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Urea production reporting

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Urea production reporting

New postby aliazharch» Mon Apr 01, 2013 10:30 am
Dear Friends,

At our Urea plant, 3 different totalizers are available for urea production reporting i.e Ammonia totalizer, CO2 totalizer and Weigh scale totalizer. However, we use Ammonia totalizer to declare the production due to its consistency in accuracy.

Has anyone of you used Weigh scale totalizer for declaring Urea production?
aliazharch
Posts: 10
Joined: Mon Dec 20, 2010 11:33 am
Location: Pakistan
Title: Sr. Executive (Process)
First name: Ali
Last name: Azhar
Department: Technical services
Company: FFBL
Country: Pakistan
Urea Plant Technology: Stamicarbon
Final product: Granules




Re: Urea production reporting

New postby Basheer» Mon Apr 08, 2013 12:26 pm
to my knowledge, Ammonia mass flow meter is used to declare the production on daily basis. However, production test is carried out every 2 months by using the trucks weigh scale and hence coreect the ammonia to urea ratio.

regards
Basheer Ali Al-Awami
Saudi Arabia
T +966 (3) 340 6160
F +966 (3) 340 6217
User avatar
Basheer
Posts: 3
Joined: Mon Mar 16, 2009 6:58 am
Title: Director - Technical Operation (Urea)
First name: Basheer
Last name: Al-Awami
Department: Fertilizer Manufacturing Unit
Company: Sabic
Country: Saudi Arabia
Urea Plant Technology: Stamicarbon and Snam
Final product: Granules


Re: Urea production reporting

New postby norozi1972» Mon Apr 08, 2013 2:28 pm
Dear Freind
I think , final weigher that located on the belt before urea storage can be useful for declaring of production.
Ammonia and CO2 totalizer can help for accuracy.Test run should be done every one or two month by truck.Ammonia and CO2 totalizer is a compensative device with temprature and pressure that can be sometime wrong and have a flauctuation.
with best regard
khpc-iran
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norozi1972
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Re: Urea production reporting

New postby m.farooq» Tue Apr 09, 2013 10:21 am
dear friends,

i do agree that at urea plant all of these totallizer are used to moniteer the urea production. rate. weighing scale at belt conveyer is among good option , but there are some associated problem due to dust at bottom of prilling tower and normaly one faces problem in accuracy in dusty conditions . production test of course is important is counter check . At our plant we have preferred ammonia base production and factor of production is calibrated after production test . additionally one can use molten urea line totallizer as well
regards.




Calculation of Urea Production

New postby alokjaiswal» Mon Sep 02, 2013 6:35 am
Dear all,

I wish to know
1. How the Urea Production is calculated?
2. If it is calculated from Ammonia flow-meter, then how the accuracy of flow-meter is checked i.e. the physical Urea matching with calculated Urea.

Regards,

Alok
alokjaiswal
 
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First name: Alok
Last name: Jaiswal
Department: Technical
Company: IFFCO
Country: India
Urea Plant Technology: Stamicarbon
Final product: Prills



Re: Calculation of Urea Production

New postby GIRISH PRAKASH» Mon Sep 02, 2013 12:23 pm
Dear Alok,

It may not be accurate to calculate the Urea production from ammonia flowmeter rate.

Regards,
Girish
GIRISH PRAKASH
Experienced
 
Posts: 124
Joined: Fri Oct 23, 2009 4:40 am
First name: GIRISH
Last name: PRAKASH
Department: Manager - Urea
Company: Tata Chemicals Ltd., Babrala
Country: India



Re: Calculation of Urea Production

New postby norozi1972» Mon Sep 02, 2013 3:16 pm
dear friend
there are many ways for calculation of urea production:
1-by ammonia consumption
2-by co2 consumption
3-by concentrated urea flow meter that installed before first urea evaporator or after final evaporators .
4-by weigher installed on the belt before going to product storage.
all mentioned ways can accurate with a direct or indirect test run minimum per month.
with best regard
norozi
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TRe: Calculation of Urea Production
New postby Reduxe» Tue Sep 03, 2013 12:24 am
Dear All
Urea Production is digitally calculated by a weight cell located in the final belt before the storage house. But there is some deviation between the actual production and the main plant load so we compare it by using the NH3 feed flow meter which gives us the main flow during the operation day ( 45 T/D )
45 * 24 = 1080 T of NH3 consumption
1080/0.566 = 1908 T of Urea produced ( every one ton of urea produce by reaction of 0.566
Ton of NH3 )
So the load of urea plant is
1908/17.5 = 109.03 %
So we compare the result with the actual production then we make a factor which controls that process ( you need to check that factor during operation )
All the above calculations can be made by using CO2 flow meter also ( every one tone of urea produced by react of 0.733 Ton of CO2 ) .
Thank you
 
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Country: Egypt
Urea Plant Technology: Stamicarbon
Final product: Granules



Re: Calculation of Urea Production

New postby alokjaiswal» Thu Sep 05, 2013 10:58 am
Dear all,

As rightly mentioned, Urea production can be calculated by Ammonia from specific consumption of 0.566 MT/MT or by CO2 from specific consumption of 0.733. But again I have some doubts.
1. Will it not be accurate to take Ammonia or CO2 losses into account?
2. If any Industry is taking losses into account, then how much is being taken into account?
3. What about ammonia flow-meter reading? How much accurate is its reading owing to the fact that ammonia is highly volatile.

Request industry professionals to share their experience.

Regards,
Alok
alokjaiswal
 
Posts: 2
Joined: Sat May 12, 2012 4:46 am
Title: Mr
First name: Alok
Last name: Jaiswal
Department: Technical
Company: IFFCO
Country: India
Urea Plant Technology: Stamicarbon
Final product: Prills



Re: Calculation of Urea Production

New postby GIRISH PRAKASH» Sat Sep 07, 2013 4:02 pm
Dear Alok,

If you do not take the losses into account, the declared production will be always inaccurate. It is very easy to account for the losses. As far as ammonia metering is concerned, the accuracy also depends on the type of flowmeter used for measuring the flow.

Regards,
Girish
GIRISH PRAKASH
Experienced
 
Posts: 124
Joined: Fri Oct 23, 2009 4:40 am
First name: GIRISH
Last name: PRAKASH
Department: Manager - Urea
Company: Tata Chemicals Ltd., Babrala
Country: India



Re: Calculation of Urea Production

New postby KASHIF NASEEM» Sat Sep 14, 2013 8:03 pm
Carry out the actual load test and record the values of flow meters on monthly basis and find the optimum consumption ratios and then use these ratios to calculate the urea production.
Before load test calibrate the flow meters as per instrumental compensation factors.
MUHAMMAD KASHIF NASEEM
SR.PROCESS ENGINEER
SAUDI BASIC INDUSTRIAL CORPORATION (SABIC)
KINGDOM OF SAUDIARABIA
naseemce@yahoo.com
+966596560770

Annex IV Guidance for assessment of representativeness and reliability of baseline environmental attributes

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Methods of Monitoring and Analysis


Annex IV
Guidance for assessment of representativeness and reliability of baseline environmental attributes
(Also Please Refer CPCB Guidelines on Methods of Monitoring and Analysis)
Attributes
Sampling
Measurement Method
Remarks
A.Air Environment
Network
Frequency


Meteorological
        Wind speed
        Wind direction
        Dry bulb temperature
        Wet bulb temperature
        Relative humidity
        Rainfall
        Solar radiation
        Cloud cover
        Environmental Lapse Rate

Minimum 1 site
in the project impact area


1 hourly continuous



Mechanical/automatic weather station



Rain gauge
As per IMD specifications
As per IMD specifications

Mini Sonde/SODAR
IS 5182 Part 1-20
Site specific primary data is essential



Secondary data from IMD, New Delhi

CPCB guidelines
Pollutants
        SPM

10 to 15 locations in the project impact area

24 hourly twice a week
(Please refer

Gravimetric (High-Volume)
Monitoring Network
        Minimum 2 locations in upwind side, more sites in downwind side / impact zone
        RPM

National Ambient Air Quality Standards, CPCB
Gravimetric (High-Volume with Cyclone)
        All the sensitive receptors need to be covered
        SO2

Notification dated 11th April, 1994)
EPA Modified West & Gaeke method
Measurement Methods
        NOx


Arsenite modified Jacob & Hochheiser
As per CPCB standards for NAQM, 1994
        CO

8 hourly twice a week
NDIR technique

        H2S*

24 hourly twice a week
Methylene-blue

        NH*3


Nessler�s method

        HC*


Infra Red analyser

        Fluoride*


Specific Ion meter

        Pb*




*Project Specific �������������������������������������������������������������������������� ����������� ��������

Note: For Rapid Environmental Impact Assessment one complete season data except monsoon is adequate while the comprehensive Environmental Impact Assessment Resources coverage of three seasons

Guidance for assessment of representativeness and reliability of baseline environmental attributes

Attributes
Sampling
Measurement Method
Remarks
B. Noise
Network
Frequency


        Hourly equivalent noise levels
Identified study area
Once in each season
Instrument : Noise level meter
IS:4954-1968 as adopted by CPCB
        Hourly equivalent noise levels
Inplant (1.5 metre from machinery)
Once
Instrument : Noise level meter
CPCB/OSHA
        Hourly equivalent noise levels
Highways
Once in each season
Instrument : Noise level meter
CPCB/IS:4954-1968
        Peak particle velocity
150-200m from blast site
Once
PPV meter



C.Water




Parameters for water quality
        pH, temp, turbidity, magnesium hardness, total alkalinity, chloride, sulphate, nitrate, fluoride, sodium, potassium, salinity
        Total nitrogen, total phosphorus, DO, BOD, COD, Phenol
        Heavy metals
        Total coliforms, faecal coliforms
        Phyto plankton
        Zoo plankton
        Set of grab samples during pre and post-monsoon for ground and surface water for 10 km distance
Diurnal and Season wise
Samples for water quality should be collected and analysed as per :
        IS : 2488 (Part 1-5) methods for sampling and testing of Industrial effluents
        Standard methods for examination of water and wastewater analysis published by American Public Health Association.


Guidance for assessment of representativeness and reliability of baseline environmental attributes

Attributes
Sampling
Measurement Method
Remarks

Network
Frequency


For River Bodies

        Total Carbon
        pH
        Dissolved Oxygen
        Biological Oxygen Demand
        Free NH4
        Boron
        Sodium Absorption Ratio
        Electrical Conductivity


        Standard methodology for collection of surface water (BIS standards)

        At least one grab sample per location per season


        Yield of water sources to be measured during critical season
        River Stretch within project area be divided in grids (say 1 km length and 1/3 width) and samples should be from each grid at a time when the wastewater discharged by other sources of pollution is expected to be maximum



Samples for water quality should be collected and analysed as per :
        IS : 2488 (Part 1-5) methods for sampling and testing of Industrial effluents
        Standard methods for examination of water and wastewater analysis published by American Public Health Association.


Data should be collected from relevant offices such as central water commission, state and central ground water board, Irrigation dept.



Guidance for assessment of representativeness and reliability of baseline environmental attributes

Attributes
Sampling
Measurement Method
Remarks

Network
Frequency


Parameters for wastewater characterisation
        Temp, colour, odour, turbidity, TSS, TDS
        pH, alkalinity as CaCO3, p value, M value, total hardness as CaCO3, chloride as Cl sulphate as SO4, Nitrate as N O3, Fluoride as F, Phosphate as PO4, Chromium as Cr. (Hexavalent, total) Ammonical Nitrogen as N, TKN, % sodium, BOD at 20�C, COD, DO, total residual chlorine as Cl2, oil and grease, sulphide, phenolic compound
        In plant sources
        Grab and
compositesampling
        Diurnal and season wise variation
Samples for water quality should be collected and analysed as per :
        IS : 2488 (Part 1-5) methods for sampling and testing of Industrial effluents
Standard methods for examination of water and wastewater analysis published by American Public Health Association.
All plant sources categorised as :
        Process wastewater
        ETP wastewater
        Domestic/sanitary wastewater






Contd...

Guidance for assessment of representativeness and reliability of baseline environmental attributes

Attributes
Sampling
Measurement Method
Remarks

Network
Frequency


D.Land Environment




Soil
        Particle size distribution
        Texture
        pH
        Electrical conductivity
        Cation exchange capacity
        Alkali metals
        Sodium Absorption Ratio (SAR)
        Permeability
        Water holding capacity
        Porosity
One surface sample from each village, (soil samples be collected as per BIS specifications)
Seasonwise
Collected and analysed as per soil analysis reference book, M.I.Jackson and soil analysis reference book by C.A. Black

Land use/Landscape
        Location code
        Total project area
        Topography
        Drainage (natural)
        Cultivated, forest, plantations, water bodies, roads and settlements
At least 20 points along the boundary

Global positioning system


Topo sheets
Satellite Imageries* (1:25,000)
Satellite Imageries*
(1:25,000)

*Project specific


Contd...


Guidance for assessment of representativeness and reliability of baseline environmental attributes

Attributes
Sampling
Measurement Method
Remarks

Network
Frequency


Solid Waste




Domestic Waste
        Per capita contribution
        Collection, transport and disposal system
        Process waste
        Quality (oily, chemical, biological)
Grab and composite samples
Seasonwise
Guidelines
IS 9569 : 1980
IS 10447 : 1983
IS 12625 : 1989
IS 12647 : 1989
IS 12662 (PTI) 1989

Quality
        Loss on heating
        pH
        EC
        Calorific value, metals etc.
Grab and composite samples
Seasonwise
Analysis
IS 9334 : 1979
IS 9235 : 1979
IS 10158 : 1982

Hazardous Waste
        Permeability and porosity
        Moisture pH
        Electrical conductivity
        Loss on ignition
        Phosphorous
        Total nitrogen
        Cation exchange capacity
        Particle size distribution
        Heavy metal
        Arsenic
        Fluoride
Grab and composite samples

Analysis
IS 9334 : 1979
IS 9235 : 1979
IS 10158 : 1982





Contd...

Guidance for assessment of representativeness and reliability of baseline environmental attributes

Attributes
Sampling
Measurement Method
Remarks

Network
Frequency


E.Biological Environment
Aquatic
        Primary productivity
        Aquatic weeds
        Enumeration of phyto plankton, zoo plankton and benthos
        Fisheries
        Diversity indices
        Trophic levels
        Rare and endangered species
        Marine Parks/ Sanctuaries/ closed areas /coastal regulation zone (CRZ)
Terrestrial
        Vegetation-species list, economic importance, forest produce, medicinal value
        Importance value index (IVI) of trees
        Fauna
        Considering probable impact, sampling points and number of samples to be decided on personal judgement within 10/25 km radius from the proposed site
        Samples to collect from upstream and downstream of discharge point, nearby tributaries at down stream, and also from dug wells close to activity site
Season wise
Standard techniques (APHA et. al. 1995, Rau and Wooten 1980) to be followed for sampling and measurement
        Seasonal sampling for aquatic biota
        One season for terrestrial biota, in addition to vegetation studies during monsoon season
        Preliminary assessment
        Microscopic analysis of plankton and me bents, studies of macro fauna, aquatic vegetation and application of indices, viz. Shannon, similarity, dominance IVI etc.
        Point quarter plot less method for terrestrial vegetation survey
Contd...

Guidance for assessment of representativeness and reliability of baseline environmental attributes


Attributes
Sampling
Measurement Method
Remarks

Network
Frequency


        Avi fauna
        Rare and endangered species
        Sanctuaries / National park / Biosphere reserve
        Migratory routes

        For forest studies, direction of wind should be considered while selecting forests


        Secondary data to collect from Government offices, NGOs, published literature
        Plankton net
        Sediment dredge
        Depth sampler
        Microscope
        Field binocular
F. socio-economic




        Demographic structure
        Infrastructure resource base
        Economic resource base
        Health status : Morbidity pattern
        Cultural and aesthetic attributes
        Education
Socio-economic survey is based on proportionate, stratified and random sampling method
Minimum for two phases of the project
Primary data collection through questionnaire
Secondary data from census records, statistical hard books, topo sheets, health records and relevant official records available with Govt. agencies
 

Natural Gas Testing

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Natural Gas Testing

Natural gas testing expertise.

Intertek laboratories provide natural gas quality and component analysis. Natural gas testing includes the analysis of conventional and shale gas, LNG, and other hydrocarbon condensates and components. Gases analyzed include hydrocarbons (C1 to C6+) such as methane, ethane, propane, iso-butane, n-butane, iso-pentane, n-pentane, and hexane, plus heavier molecules.
Natural gas labs test to trace detection levels for impurities. Natural gas trace impurities include hydrogen, nitrogen, carbon monoxide, carbon dioxide, oxygen, mercury, sulfur, water, and other components.
Natural gas tests:Natural gas test methods:
Natural Gas Composition Analysis:ASTM D1945, GPA 2261, ISO 6974, UOP 539, GC-MS, etc.
Natural Gas Condensate Analysis 
Methanemol %
Ethane C2mol %
Propane C3mol %
Iso Butane C4mol %
Normal Butanemol %
Iso Pentane C5mol %
Normal Pentanemol %
Hexane plus Heavier mol %
Total C6 carbonmol %
Total C7 carbonmol %
Nitrogenmol %
Carbon Dioxidemol %
Oxygenmol %
Total SulfurASTM D5504, ISO 6326, etc.
Hydrogen SulfideASTM D5504, ISO 6326, etc.
Water                KF
Energy CalculationsASTM D3588, GPA 2172, ISO 6976
Vapor DensityCalculated
Relative Density                                Calculated
Molecular WeightCalculated
Gross Heating Value (GHV)Calculated
Net Heating Value (NHV)Calculated

 

 

SAFETY PLEDGE & HEALTH -SAFETY CULTURE & SAFETY MOVEMENT HISTORY

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very thankful to Mr. pareed kutty FOR SHARING WITH US


Health & Safety Culture
Health & Safety Culture
(A). Introduction
The purpose of this bullettin is to give you a fundamental idea about the subject “ Health and Safety Culture” and to identify and correct your behaviour, if applicable, to promote a positive Health and Safety Culture in our organization. The success or failure of EHS implementation in an organization depends on the EHS Culture existing in the organisation. If it is negative, we need to change to positive through our actions in dealing with each EHS related matters at all levels. The availability of a good EHSMS alone within an organisation does not guarantee the implementation of the same. The culture of an organization has been described as the objective characteristics about the way in which it works-its structure, rules, management style, ethics, attitudes..etc which may be observed from outside. The Health and Safety culture is recognised as being the single key driver of health and Safety performance. It reflects people’s belief and attitude towards safety. An organisation’s safety culture is the result of interactions between their systems, attitudes and perception of Safety

(B) Definition
As per , the definition of Safety Culture is as follows:
“The product of individual and group values, attitudes, perceptions, competencies and patterns of behaviour that determine the commitment to, and the style and proficiency of , an organisation’s health and safety management”.
An organisation’s safety culture has a direct impact on things like:
• The success or failure of health and safety initiatives;
• Whether employees comply with rules and procedures;
• Whether they are prepared to take risks;
• The balance between safety and production.

(C). Safety Culture ( Negative/Positive)
An organisation with a positive health and Safety culture will consist of competent people with strongly-held values which they put into practice. This will go through the whole organisation-from top to bottom. Thus, it starts with a firm statement of policy and this policy will be reflected at all levels in both the attitudes of management and employees, and the working practices and safety measures applied. There will be clear determination to control hazards and risk, and to make the workplace a safe place for all concerned. By contrast, where there is a negative safety culture, management and staff are likely to adopt only the minimum safety arrangement just to comply with the law with the aim of avoiding financial fine/warnings from govt. authorities ...etc.
A negative effect on health and Safety culture may be seen in two ways.
  􀂾 Managers at different levels will give important to production progress only and downplay safety
considerations.
􀂾 Workers will loose faith in the protection offered by safety policies and, and view management as untrustworthy and unethical in its operation. They may also seek advancement and increases in pay through demonstrating similar values to management, and thus themselves cut corners and take more risk.

(D) Internal Influence on Health and Safety Culture
There are several factors , internal to the organisation, that influence the Health and Safety culture of an organisation as well as external factors which is out of the scope of this bulletin.

The following are some of the important points :-
• Management Commitment : The level of commitment to Health and Safety is crucial to the culture of Health and Safety in the organisation
• Production Demands : Whether the Health and Safety is given enough consideration at the projects or Are employees allowed to cut corners on health and Safety issues in the project to achieve production
Targets ? The Project Manager has a very big role in this matter.
• The communication : Communications , formal and informal, existing in an organisation has good impact on safety culture. Whether EHS is addressed in each work related communications/Meetings ...etc ?
• Competence : Whether staff are competent to work safely ? Whether training , appropriate to the nature of the individual’s health & Safety Role, is provided to the employees?
Now, I am giving below some of the examples which i have observed in some of my previous employment with another organisation/subcontractors . This is for you to think and analyse whether it is a part of a negative safety culture or not ?

􀂙 Visiting of a senior manager ( Example: Project Managers/ any other senior Manager ) to the construction site without wearing hard hat. The rest of his subordinates wear it. Does it not an indicator of Negative Safety Culture ? ( What messagegoes to subordinate’s mind about Health and Safety. Just Think. “Do what i say, not what i do” message is a negative safety culture )
􀂙 Internal Safety Training ? Yah. It can be conducted, but, only in the rest time/Lunch time of the people, not on duty time.
The reason is that Safety training will interrupt the production progress. Is it a positive sign or Negative sign with regard tohealth and Safety culture? Sure. It is negative. The benefit of Safety Training is not considered here. Also, safety is notconsidered as an integral part of the work, Safety is considered as an unwanted element or just to satisfy somebody.
􀂙 Safety Implementation ? Yah. We do it. We have safety Plan and Safety Officer. They do it. ? What it indicates ? A Negative Or positive Safety Culture ? Pls Think.

􀂙 If the safety is not implemented properly at site, the concerned Manager call the EHS officer and shout him in front of thefrontline supervisors without asking the frontline supervisors about it. Is it a part of a positive safety culture ? I can assureyou that Health and Safety will never improve in that organisation till this attitudes are changed/corrected about EHS.
􀂙 A secret agenda between a manager and his foremen/Engineer to bypass EHS procedure for more production. Is it Positive?
􀂙 Yes, We have to implement safety in the site to avoid financial fine from authorities (Municipality, RTA...etc). Is it the main
objectives of implementing safety ? If no fine, no need of safety at site!! Is it right ?
The above are only some of the examples and we can give a lot more. These examples are just for you to think about Health and
Safety Culture .


(D) Conclusion
The promotion of positive Safety culture is a very important subject to look into when we are serious about safety implementation. A change of safety Culture is possible with everybody’s cooperation and with strong back up of management. Normally, change of safety culture does not happen very soon as overcoming of resistance/ Changing of attitude from strong minded persons requires time with management’s involvement from time to time. Please remember – A wrong thing is wrong thing even if we have been practicing it in this way since many years.
If the above descriptions are applicable to us, it is the time to think about a change of mindset to develop a positive culture

(E) Wearing PPE – How to create a Positive culture
Now Let us take the case of wearing PPE at the site. In order to develop a positive culture in this regard,what are the recommendations. It can be something like below
􀂾 The Engineers, Managers and Supervision staff to set an example by wearing PPE at the project
􀂾 Training to the employees- About the benefits of wearing PPE
􀂾 Consult and communicate with the workforce in the selection of PPE . This can be done through toolbox talk.
􀂾 Listen to their problems/barriers, if any, to wear PPE and reach to a decision
􀂾 Motivate the labours to wear PPE by giving safety award and Cash Award to selected labours who wear PPE always
􀂾 In case a worker does not wear PPE, the supervision staff to take action first and inform safety officer.
􀂾 Make Available the PPE at the store. No exemption for not wearing PPE at any time. No reasons accepted

Vedkal                         Yajurved, Rugved, Upnishads etc. Old concept of science and safety in nation. Our ancient heritage.
BC 3500                      Medhatithi of Bharat discovered decimal system.
BC 3000                      The Ebers Papyrys and the Edwin Smith Papyrus, the first written document on health and safety.
BC 2000                      Chanakya Kautilya's Arthshastra dealing many subjects including safety. See Part-5.1 of Chapter-1.
BC 2000                      Babylonian code of Hammurabi of some 280 paragraphs covering bodily injuries and workers' compensation laws.
BC 1500                      Ramses III hired Physicians to care for mine and quarry workers.
BC 1000                      Acharya Dhanvantari invented 'Pharmacy' and Sushrut  'surgery'. Bhrugu shilp Sahitya on many branches of Engineering.
BC 800                        Bodhayan's Shalvasutra - Principle of right angle.
BC 680                        Invention of 'atom' by Kanad muni.
BC 427-347                Pleto's teaching of mathematics and globe shapes of all planets.
BC 400                        Hippocrates, known as the father of medicine described tetanus.
BC 384-322                Philosophy of science by Aristotle.
BC 320                        Indian sword gifted to Alexander.
BC 287-212                Displacement of water, buoyancy and specific gravity by Archimedes.
BC 200                        The effects of lead poisoning were described by the Greek poet and physician Nicander.
BC 100 to 2nd             Various Roman writers described the plague of Athens, the ill effects of their
Century                        environment on mine workers and unhealthful effects of lead for water piping and wine containers.
100-178                       Ptolemy who told that the Sun moves around the earth. His book, 'The Great Treatise  of  Astronomy'.  He  gave mathematical models.
650                              Aryabhatttoid thatSun'shines themoon and earth rotates. This results in day and night;
Fifth                             Aryabhatt's contribution in Mathematics.
Century                        His discovery of D (22/7), sine, cosine etc.
Eight                             Nagarjun's book 'Ras ratnakar' on Chemistry.
Century
700-800                       In Lombardy, King Rothari codified the laws in 388 chapters on principles of compensation for injury. Bhaskaracharya's 'Lilavati Ganit' i.e. Algebra and Law of Gravitation.
1456                            First printing press in Germany  by Gutenberg.
1473-1543                   Nicolas Copernicus told that the Sun is the centre and the Earth and other planets move around it. This was told by Aryabhatta many years ago in 650. .
1473                            Ulrich Ellen bag, an Austrian physician warned about hazards of metal burning.
1561                            George Agricola's book described air venting in mines and use of gloves, leggings and masks.
1564-1642                   Galileo who discovered equal speed of falling bodies, telescope and reaffirmed Copernicus' Sun-centered principle.
1567                            Paracelsus published On the 'Miners' Sickness  and  other  Miners'  Diseases, distinguishing acute and chronic poisoning.
1571-1630                   Kepler who stated the elliptical motion of planets around the Sun.
1642-1727                   Issac Newton. Principles of gravity, rules of light, optics, calculus etc.
1701-1800                   Industrialisation (Mills) started in Britain and spread to the Continent and USA.
1732                            First  spinning  machine  by  Richard Arcright. Pioneer of industrial revolution.
1749-1838                   John Stevance, Father of American Railways.
1761-1828                   Nicolas Lui Rober, pioneer of paper industry.
1764                            Discovery- of spinning jenny.
1765                            Steam engine by James Watt.
1765-1825                   Aley Whitney produced sewing, washing and other machines.
1768-1835                   Sernual Sletor, Father of American cloth industry.
1771-1852                   David Wilkinson, Father of machine tools industries.
1784                            Discovery of powerlooms.
1792                            Discovery of cotton gins.
1796                            Dr. Edward Janner, Small Pox vaccination.
1800-1860                   Charls Goodyear, Father of rubber industry.
1801-1874                   Gail Borden, Father of modern dairy technology.
1804                            President Thomas Jefferson delivered his safety message to Captain Merriwether Lewis.
1806-1873                   John Stuart Mill, the great contributor in philosophy of science.
1807                            Steam ship by Robert Fulton.
1809-1884                   Sirus  Hall  McCormick,  Father  of agriculture industry.
1813-1818                   Sir  Henri  Bessimer,  Father  of steel industry.
1814                            Locomotive engine by James Watt.
1819-1880                   Edwin L. Derek, Father of Petroleum industry.
1825                            Railway usage began.
1830-1850                   First attempt to legislate the working hours of women and children in Great Britain.
1831-1879                   James Clerk Maxwell, Electromagnetic waves which led us to Radio and TV.
1832-1891                   Nicholas August Auto discovered internal combustion engine. Father of automobile industry. Great contribution to industrial revolution.
1833                            England, Govt. Factory Inspectorate established.
George Stephenson suggested use of a steam whistle on locomotives.
1834                            England, law enacted to provide fencing for mill gears and shafts. Lord Ashley's Great Factory Act.
1844-1929                   Karl Benz made first motor car and called Father of motor car industry.
1845-1923                   Wilhelm Rontgen, discovery of X-ray. First Nobel Prize winner in 1901.
1847-1922                   Alexander Greham Bell discovered Telephone.    Called    Father    of telecommunication.
1847-1931                   Thomas Alva Edison, Father of electrical industry.
1847-1937                   Gugli Eimo Marconi discovered wireless telegraph and called father of wireless telegraphy.
1855                            Insurance  Protection against boiler explosions was afforded in England.
1858-1913                   Rudolf Diesel discovered diesel fuel and called father of diesel industry.
1858-1932                   Dr Jagdish Chandra Bose. Sensation of plant. Cresco graph to view enlargement of plant movement.
1863-1914                   Charles Martin Hall obtained pure aluminum and called father of aluminum industry.
1864                            First accident insurance policy in North America.
1865                            Benzene ring structure.
1866                            National Board of Fire under-writers.
1867                            Massachusetts had begun to use factory inspectors.
Boiler and machinery insurance, started in USA.
1869                            Germany-Acts passed providing that all employers furnish necessary appliances to safeguard health and life of employees. Massachusetts (USA) established, the first state bureau of labour statistics in order to determine the kinds and causes of accidents.
Periodic Table of elements by Mendelif.
1870                            Westing house airbrake adopted by the railroads.
1872                            First electric automatic signal installed on the Pennsylvania rail board.
1873-1961                   Lee De'Forest discovered radio and called father of radio industry.
1874                            France, Law enacted providing for special inspection service of workshops.
1876-1920                   Willis Havilland Carrier discovered airconditioning and called father of airconditioning industry.
1877                            Massachusetts. Law passed compelling guarding of dangerous moving machinery.
1879-1955                   Albert Einstein. Quantum theory and principles of relativity.
1879                            Electric bulb by Thomas Alva Edison.
1880                            American Society of Mechanical Engineers.
1881                            American National Red Cross.
First Indian Factories Act.
1885                            Germany Alabama, passed employers' liability law.
Germany, Bismarck prepared and enacted the first Compulsory Compensation Act for workers. This Act covered only sickness.
1887                            Massachusetts passed an employers' liability law.
Ervin Schrodinger - wave mechanics.
1890                            First international conference in Berlin of 15  European  States  to  draw  up international conventions on labour regulations.
Establishment of International Association for the Legal Protection of Workers, the forerunner of the ILO which was established in 1919.
1892                            Safety Department of the Joliet Works of the Illinois Steel Company formed. This has been called "The birthplace of the American industrial accident prevention movement". The first safety order was the inspection of all engine flywheels.
1893                            Federal Safety Appliance Act required use of standard safety equipment on railroad.
1896                            National Fire Protection Association (NFPA), USA.
Radioactive elements by Cury couple.
1900                            US Census of 1900 showed 1750178 working children between 10 to 15 years. Quantum theory by Mex Planck. First safety periodical 'Safety Maintenance' published by Alfred M. Best company.
1901                            National Bureau of Standards.
1903                            First steel passenger car constructed. Demands of industrial workers were considered in Russia.
1905                            Extension of Quantum theory by Einsteine.
1907                            Quarterly of the National Fire Protection Association published by NFPA.
1908                            Transportation of Dangerous Explosives Act passed.
1909                            Aeroplane by Orvil and Vilbar Right brothers.
First National Conference on Industrial Diseases held.
1910                            The oldest large Occupational Health Institute "The Clinica del Lavoro" in Milan.
1911                            New Jersey First State Workmen's compensation law passed.
California passed the first American law for   the  compulsory   reporting  of occupational diseases.
AmericanMuseum of Safety.
Ernest Rutherford - Concept of Nucleus and electron in atom; alpha, beta and gamma rays and many inventions on atomic energy.
1912                            Discovery of Thorium, Polonium and Radium by Madam Curry.
1913                            Bureau of Labour Statistics.
'Safety'  published by  the  AmericanMuseum of Safety.
Atomic structure, Nuclear structure and Atomic Model by Nisbohr.
National Safety Council was founded in USA.
1914                            The first World-War started accelerating industrialization and need of safety.
The first safety of life at sea convention held in London.
1915                            American Society of Safety.
Elliptical  motion  of  electrons  by Summerfield.
1918                            Air Mail Service started.
1919                            National Railroad Accident Prevention Drive inaugurated.
National Safety News published by the National Safety Council. Then many other publications-started in the subsequent years by NSC (USA).
International Labour Organi-sation (ILO) was established at Geneva, Switzerland. Hours of Work (Industry), ILO Con.l, Unemployment Con.2, Recom 1, Maternity Protection Con.S, Night Work (Women) Con:4, Minimum Age (Industry) Con.5, Night Work of Young Persons (Industry) Con.6, Anthrax prevention Recom 3, Lead ' Poisoning Recom 4, .Labour Inspection Recom 5, White Phosphorous Recom 6
1921                            ILO at Geneva set up a safety service. White Lead, ILO Con. 13, Weekly Rest (Industry) Con. 14.
1922                            Greenburg and Smith introduced the impinger, a dust sampling device, which resulted in the impinger method becoming the standard for the US Bureau of Mines and the Public Health Service.
1923                            Labour Inspection ILO Recom 20
1925                            Workmen's Compensation ILO Con. 17 to 19 and Recom 22 to 25.
1926                            Bensol, Poisoning study.
4:1 accident cost ratio presented by H.W. Heinrich.
First rocket fly.
1927                            A study of the relation between safety and production was made by the American Engineering Council in 1926 and 1927.
1928                            First National Aromatic Safety Conference held in America.
American Standards Association.
Functioning of International Commission on Radiological Protection (ICRP).
1929                            The US Load Line Act passed to prevent overloading of cargo under various conditions.
The foundation of a major injury ratio 30029-1 indicated by H.W. Heinrich. Peniciline by Alexander Flemming.
Prevention of Industrial Accidents ILO Recom 31
Power driven machinery, ILO Recom 32
1930                            First Greater New York Safety Conference held in New York city. It was a one day session with 900 attendence.
1930-1934                   The ILO published its first Encyclopedia "Occupation and Health", the value of which was widely recognized.
1934                            Bureau of Labour Standards.
Workmen's Compensation revised, ILO
1908                            The Air Hygiene Foundation was created to conduct scientific studies to prevent occupational diseases and industrial health. 40 Hours Week, ILO Con. 47.
1936                            Holidays with Pay, ILO Con. 52, Recom 47.
1937                            Automotive Safety Foundation.             
National Committee on Films for Safety. Safety Provisions (Building), ILO Con.62, Recom 53 to 56.
1938                            Centre for Safety Education.                 
Nuclear Fission of Uranium by Farmy and Han.                       
1939                            American Industrial Hygiene Association. Labour Inspectorates, ILO Recom 59.
1940-150                     Inclusion of Modern Defense Equipment viz.. Radar, jet aircraft, missiles, atom      bomb, computer etc.
1941                            Industrial Hygiene Departments set up in 33 States (USA).
The Accident Cause Code was completed by USA. This code introduced an era of    accident cause standardization in USA overcoming a weakness in industrial accident prevention that had long existed. National Bureau for Industrial Protection (USA).
1944                            Medical Care, ILO Recom 69.
1945                            SolidState Transistor by Bell Telephone Laboratories of America. Ultimately this solid state electronics has now come upto the stage of microelectronics using silicon chips and integrated circuits.
America threw atom bombs on Hiroshima and Nagasaki of Japan causing @ 1,20,000 deaths and more injuries in Aug 1945.
Tata Institute of Fundamental Research in atomic energy at Bombay.
DGFASLT. i.e. Directorate General. Factory Advice Service and Labour Institute was set up at Delhi. It was shifted toBomba) (the CLI building) in 1966.
Foundation of International Air Transport Association (IATA) in Switzerland.
1946                            Medical Examination of young person? (Industry & Non-industry), ILO Con.77-79 and Recom 79.
The oldest Occupational Health Service ii France. Then in Japan in 1947.
1947                            Establishment,    of    International Organisation for Standardi-sation (ISO) by ILO on 24-2-1947. ISO, work is carried out through some 2000 technical bodies and 100000 experts from all over the world More than 4000 International Standard have been published in some 30000 pages Labour Inspection, ILO Con. 81,85, Recom 81, 82.
ILO  conference  adopted  the  first International Standards Concerning the organisation of labour inspection. Atomic Energy Commission (USA).
1948                            Declaration of Industrial Policy for small scale industries and public sectors on 6-41948.
Atomic Energy Commission.
1949                            The first national Ergonomics Research Society in UK.
The ILO published a model code of Safety Regulations for Industrial Establishments for the guidance of Governments and Industry.
1950-60                       Establishment of Indian Institutes of Technology at Kharagpur, Bombay, Madras, Delhi and Kanpur, Defense organization. Council of Scientific and Industrial Research and Department of Technology in our country.
1952                            Pesticides manufacturing started in India. Social Security (Minimum Standards) ILO Con.102
1953                            Protection of workers health, ILO Recom 97 (It includes technical as well as medical measures and compulsory notification of occupational diseases).
1954                            Atomic battery (giving crores of electrons per second on transistor wafer) by USA. Atomic Energy Centre was established at Trombay in Bombay. This was renamed as Bhabha Atomic Research Centre in 1967.
1955                            Dr. Bhabha was selected as President of the conference on the Peaceful Uses of Atomic Energy at Geneva.
1956                            Our first nuclear reactor 'Apsara', the first in Asia also.
Welfare facilities, ILO Recom 102
1957                            Sputnic the first satellite in the sk/ by Russia.
Formation of International Committee for Lifts Regulations (CIRA) in Switzerland. International Atomic Energy Agency (IAEA) came into existence on 29-7-1957 by the statute of United Nations.
1958                            Defense Research and Development Organisation. Approval of National Policy on Scientific Research and Development by the Parliament on 4-3-58.
1959                            Occupational Health Service, ILO Recom 112.
Birth of International Ergonomics Association (IEA) on  6-4-1959 in Oxford. International Occupational Safety and Health Information Centre (CIS) was set up by the ILO Office in May 1959 to collect, disseminate, co-ordinate and distribute world-wide information on occupational safety and health. The service was computerised since 1974. Direct access to CIS data via display terminals and variety of publications are available.
1960                            The Regional Labou" Institute (RLI), Madras was set up.
Radiation Protection, ILO Con.llS, Recom 114.
1961                            The Central Labour Institute (CLI) started in a rented building in 1961 and shifted to its Sion-Bombay premises in 1966.                
1962                            The Regional Labour Institute (RLI), Kanpur was set up.                      
1963                            Guarding of Machinery, ILO Con.ll9, Recom 118.
1964                            Hygiene (Commerce & Offices) ILO Con.l20, Recom 120. Employment Injury    Benefit ILO Con. 121 Recom 121.
1965                            The Regional Labour Institute (RLI), Calcutta was set up. Formation of International Agency for Research on Cancer by WHO.
Medical examination of young persons (underground work) ILO Con. 124.
1966                            The National Safety Council (NSC) was established on 4th March 1966, at CLIBuilding, Sion,  Bombay-22.  In  this remembrance, 4th March is celebrated as the National Safety Day in our country.       
Electronics Committee at the Chairmanship of Dr. Vikram Sarabhai.
First tidal electric plant in France giving 5000 Kwh electricity per year. 
Foundation of the International Radiation    1978 Protection Asso-ciation (IRPA) in France.
1967                            Maximum Weight, ILO Con.l27, Recom 128.
1968                            Two conventions on Road Traffic and Road Signs and Signals in Vienna.
Agreement on the International Transport of Dangerous Goods by Road (ADR) came into force on 29-1-1968 at Geneva.
1969                            Atomic Power Station at Tarapur in Maharashtra.
Apollo - II landed on the moon with three scientists, on 21-7-69..
DAE-NASA Satellite - I TV experiment. Report of the National Commission of    Labour, India, 1969.
Medical care and Sickness benefits, ILO Con. 130, Recom 134.
A meeting of editors and users of occupational safety and health periodicals from 21 countries at Geneva on 7-8 July 1969.
1970                            Establishment of International Nuclear Information System (INIS) by the IAEA started in 1957.
1971                            Electronics  Commission  under  the President ship of Dr. Menon.
The Division of Nuclear Safety and Environment Protection started as a division of IAEA.
Starting of programme of evaluation of chemical carcinogenic risk to humans. Starting of Science and Technology Department by the Central Government. Benzene, ILO Con.l36, Recom 144.
1972                            Foundation of International Association of Labour Inspection (IALI) in Switzerland.
1974                            Atomic explosion (experiment) in the desert of Rajasthan.
Occupational Cancer, ILO Con.139, Recom 147.
1975                            Combination of two space shuttles Apollo (USA) and Soyuz (USSR) in the sky.
1976                            Landing of Viking-1 & 2 (USA) on the Mars. Launching of PIACT (International Programme for the Improvement of working conditions and environments). Legislation - The Toxic Substances Control Act 1976 (TSCA) in USA.
International Occupational Safety and Health Hazard Alert System was adopted by the International Labour conference.
1977                            Gujarat Safety Council was registered on 52-1977 at Vadodara.
Working Environment (Air pollution, Noise and Vibration) ILO , Con.148, Recom 156.
1978                            International conference on primary health care sponsored by WHO & UNICEF on 129-78.
Labour Administration, ILO  Con.150, Recom 158.
Identification  of  4039907  chemical compounds by the American Chemical Society's Chemical Abstract Service (CAS).
1979                            Occupational Safety & Health, Dock Work, ILO Con.l52, Recom 160, Hours of Work & Rest Periods (Road Transport) ILO Con.l53, Recom 161.
Publication of Initial Chemical substances inventory listing 44000 chemicals, by USA.
1980                            The International Programme on Chemical Safety (IPCS) became operational in June 1980, at WHO Head quarters. It is a cooperative venture by UNEP (United Nations Environment Programme), ILO and WHO.
1981                            Occupational Safety & Health, ILO, Con.l55, Recom 164.
1982                            Maintenance of Social Security Rights, ILO Con.l57. Recom 167.
1985                            Labour statistics, ILO, Con.l60. Recom 170.    1996 Occupational Health Services, ILO Con. 161, Recom 171, World Environment (1985), a brochure published by Loksabha, warned about environmental problems. 'TlieState of India's Environment 1984-85, i.e. the Second Citizen's Report' also threw light on tremendous loss of environment and    1997 human health in our country (see Chap-1).
1986                            Asbestos, ILO Con.l62, Recom 172. The Environment (Protection) Act, 1986.
1987                            Vital amendments in the Factories Act, 1948 owing to Bhopal disaster.             
1988                            Safety and Health in Construction, ILO Con.l67, Recom 175.                         
1990                            The Chemicals, ILO Con.l70, Recom 177. Night Work, ILO Con. 171, Recom 178.     
1993                            Prevention of Major Industrial Accident, ILO Con.l74, Recom 181.                 
1995                            Safety & Health in Mines, ILO Con.l76 Recom 183. Vital amendments in the   Gujarat  Factories  Rules,  1963,  in consequence to the 1987 amendment in the Factories Act.
1996                            'Down to Earth' report of 15-10-96, warned about environmental losses, air and water pollution and danger to human health (see Chap-1).
'Greenpeace international' report of 10-12-96 threw light on unsafe conditions of our industries and dangers due to chemicals. 3
1997                            Landing of arobotic spacecraft. Pathfinder on 4-7-1997, on the red planet Mars by the NASA, USA.
Launching of a Satellite IRS-ID by ISRO on 29-9-1997.
1998                            IS:14489  -  Code  of  Practice  on Occupational Safety and Health Audit.
1999                            Launching of a Commercial Telecom Satellite INSET-2E by ISRO on 3-4-1999.
2001                            Safety and Health in Agriculture Con. 184, Recom 192.
2002                            List of Occupational Diseases, Recom 194.
2004                            HRD Recom 195.
2006                            IS : 15656 Hazard Identification and Risk Analysis.

PERFORMANCE STANDARD OBJECTIVES

International Women's Day Official UN Themes-Equality for Women is Progress for All

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International Women's Day
The day is an official holiday in Afghanistan, Angola, Armenia,Azerbaijan,Belarus, Burkina Faso,Cambodia, China (for women only), Cuba,Georgia,Guinea-Bissau, Eritrea,[Kazakhstan,KyrgyzstanLaos,Macedonia (for women only), Madagascar (for women only), Moldova, Mongolia, Nepal (for women only), Russia,Tajikistan,Turkmenistan,Uganda,Ukraine,Uzbekistan,[Vietnam, and Zambia.

In some countries, such as Cameroon,Croatia, Romania,Montenegro, Bosnia and Herzegovina,Serbia,Bulgaria and Chile, the day is not a public holiday, but is widely observed nonetheless. On this day it is customary for men to give the women in their lives – friends, mothers, wives, girlfriends, daughters, colleagues, etc. – flowers and small gifts. In some countries (such as Bulgaria and Romania) it is also observed as an equivalent of Mother's Day, where children also give small presents to their mothers and grandmothers.

 



Women and Hunger: 10 Facts



Women are often victims of hunger. They also have a crucial role to play in defeating hunger. As mothers, farmers, teachers and entrepreneurs, they hold the key to building a future free of malnutrition. Here are ten reasons why empowering women is such an important part of WFP’s work.
  1. In developing countries, 79 % of economically active women spend their working hours producing food through agriculture. Women are 43% of the farming work force.
  2. Yields for women farmers are 20-30 percent lower than for men. This is because women have less access to improved seeds, fertilizers and equipment.
  3. Giving women farmers more resources could bring the number of hungry people in the world down by 100 - 150 million people.
  4. Surveys in a wide range of countries have shown that 85 - 90 percent of the time spent on household food preparation is women’s time.
  5. In some countries, tradition dictates that women eat last, after all the male members and children have been fed.
  6. When a crisis hits, women are generally the first to sacrifice their food consumption, in order to protect the food consumption of their families.
  7. Malnourished mothers are more likely to give birth to underweight babies. Underweight babies are 20 percent more likely to die before the age of five.
  8. Around half of all pregnant women in developing countries are anaemic. This causes around 110,000 deaths during child birth each year.
  9. Research confirms that, in the hands of women, an increase in family income improves children’s health and nutrition.
  10. Education is key. One study showed that women's education contributed 43% of the reduction in child malnutrition over time, while food availability accounted for 26%.
                                         Women in the developing world: facts and stats
Women and climate change
Women in Dola, Nepal, construct a pond to irrigate their vegetable gardens. Photo: Tom Pietrasik.
Women make up 20 million of the 26 million people estimated to have been displaced by climate change.
Women are often hit much harder during disasters. In the Bangladesh cyclone of 1991, the number of women who died was five times greater than the number of men. They had not been taught how to swim and received no prior warning of the event. In the tsunami that hit Sri Lanka in December 2004, many more women perished than men because they did not know how to swim or climb trees.

In southwest Bangladesh, the salinisation of drinking water has meant that many women are forced to walk long distances – up to 10km every day – just to fetch water.

Droughts in the Philippines are making it increasingly difficult for women to search for food, fuel and water, all of which were previously accessible in towns. In rural areas, women and girls are being forced to walk for hours to fetch water. This makes them more prone to accidents and acts of violence.

After a food crisis, women and children often give up their meals for the men, increasing their susceptibility to malnutrition.

Increasingly unpredictable and extreme weather is affecting harvests and making it harder for the poorest people, especially women, to provide food for their families. In many developing countries, rural women produce up to 60% of household food, and are major producers of the world’s staple crops (such as rice, wheat, maize), which provide up to 90% of the rural poors' food intake.

Women and food
Oxfam is helping communities establish vegetable gardens in the Highlands of Papua New Guinea. Photo: Jerry Galea
Women produce the majority of the world’s food but do so under difficult conditions.
On Sub Saharan African farms, 75% of the workforce are women, they produce 80% of the household food but they only own 1% of the land and are rarely included in the decision making (either on agricultural production or at a household level).

Research has shown that farms run by educated women show increases in yields of up to 22%. Yet two-thirds of the children denied school are girls and 64% of the world’s illiterate adults are women.

Women worldwide rarely own land: in Sub-Saharan Africa women own 1% of the land, in Brazil they own 11% and in Peru 13%. Lack of land rights means women are frequently the ones left dispossessed and uncompensated. When women do own land, their holdings are smaller than their male counterparts – between 20% and 35% on average worldwide. Such land is often marginal and thus of low productivity.

Women face discrimination in terms of access to credit, tools, training and a variety of other agricultural services. Available figures show that only 5% of extension services have been addressed to rural women, while no more than 15% of the world's extension agents are women. In Africa women receive 7% of extension services and 10% of the credit to small-scale farmers. When women do obtain credit the average value is 42% of what is granted to male farmers, and often a much higher percentage of collateral is required (collateral that women rarely have, see earlier point).

  Women and increasing food prices

Women and children living in poverty will be hardest hit if global food prices continue to rise. In many countries it is women who are responsible for feeding their families and, when times are hard, it is women who go without to allow their husbands and children to eat.

Governments must act now and act together to help those already facing the crisis, to avert another global crisis and to help end hunger for the almost one billion people who go to bed hungry every day.

Women in the developing world: facts and stats



Women and climate change

Women in Dola, Nepal, construct a pond to irrigate their vegetable gardens. Photo: Tom Pietrasik.
Women in Dola, Nepal, construct a pond to irrigate their vegetable gardens. With this pond and drought-resistant seeds, they now have a sustainable food supply.
Women make up 20 million of the 26 million people estimated to have been displaced by climate change.
Women are often hit much harder during disasters. In the Bangladesh cyclone of 1991, the number of women who died was five times greater than the number of men. They had not been taught how to swim and received no prior warning of the event. In the tsunami that hit Sri Lanka in December 2004, many more women perished than men because they did not know how to swim or climb trees.
In southwest Bangladesh, the salinisation of drinking water has meant that many women are forced to walk long distances – up to 10km every day – just to fetch water.
Droughts in the Philippines are making it increasingly difficult for women to search for food, fuel and water, all of which were previously accessible in towns. In rural areas, women and girls are being forced to walk for hours to fetch water. This makes them more prone to accidents and acts of violence.
After a food crisis, women and children often give up their meals for the men, increasing their susceptibility to malnutrition.
Increasingly unpredictable and extreme weather is affecting harvests and making it harder for the poorest people, especially women, to provide food for their families. In many developing countries, rural women produce up to 60% of household food, and are major producers of the world’s staple crops (such as rice, wheat, maize), which provide up to 90% of the rural poors' food intake.

Women and food

Oxfam is helping communities establish vegetable gardens in the Highlands of Papua New Guinea. Photo: Jerry Galea
Oxfam is helping communities establish vegetable gardens in the Highlands of Papua New Guinea.
Women produce the majority of the world’s food but do so under difficult conditions.
On Sub Saharan African farms, 75% of the workforce are women, they produce 80% of the household food but they only own 1% of the land and are rarely included in the decision making (either on agricultural production or at a household level).
Research has shown that farms run by educated women show increases in yields of up to 22%. Yet two-thirds of the children denied school are girls and 64% of the world’s illiterate adults are women.
Women worldwide rarely own land: in Sub-Saharan Africa women own 1% of the land, in Brazil they own 11% and in Peru 13%. Lack of land rights means women are frequently the ones left dispossessed and uncompensated. When women do own land, their holdings are smaller than their male counterparts – between 20% and 35% on average worldwide. Such land is often marginal and thus of low productivity.
Women face discrimination in terms of access to credit, tools, training and a variety of other agricultural services. Available figures show that only 5% of extension services have been addressed to rural women, while no more than 15% of the world's extension agents are women. In Africa women receive 7% of extension services and 10% of the credit to small-scale farmers. When women do obtain credit the average value is 42% of what is granted to male farmers, and often a much higher percentage of collateral is required (collateral that women rarely have, see earlier point).

Women and increasing food prices

Women and children living in poverty will be hardest hit if global food prices continue to rise. In many countries it is women who are responsible for feeding their families and, when times are hard, it is women who go without to allow their husbands and children to eat.
Governments must act now and act together to help those already facing the crisis, to avert another global crisis and to help end hunger for the almost one billion people who go to bed hungry every day.
- See more at: http://www.oxfam.org.nz/what-we-do/issues/gender-equality/women-in-the-developing-world#sthash.FNHF12KV.dpuf

Women in the developing world: facts and stats



Women and climate change

Women in Dola, Nepal, construct a pond to irrigate their vegetable gardens. Photo: Tom Pietrasik.
Women in Dola, Nepal, construct a pond to irrigate their vegetable gardens. With this pond and drought-resistant seeds, they now have a sustainable food supply.
Women make up 20 million of the 26 million people estimated to have been displaced by climate change.
Women are often hit much harder during disasters. In the Bangladesh cyclone of 1991, the number of women who died was five times greater than the number of men. They had not been taught how to swim and received no prior warning of the event. In the tsunami that hit Sri Lanka in December 2004, many more women perished than men because they did not know how to swim or climb trees.
In southwest Bangladesh, the salinisation of drinking water has meant that many women are forced to walk long distances – up to 10km every day – just to fetch water.
Droughts in the Philippines are making it increasingly difficult for women to search for food, fuel and water, all of which were previously accessible in towns. In rural areas, women and girls are being forced to walk for hours to fetch water. This makes them more prone to accidents and acts of violence.
After a food crisis, women and children often give up their meals for the men, increasing their susceptibility to malnutrition.
Increasingly unpredictable and extreme weather is affecting harvests and making it harder for the poorest people, especially women, to provide food for their families. In many developing countries, rural women produce up to 60% of household food, and are major producers of the world’s staple crops (such as rice, wheat, maize), which provide up to 90% of the rural poors' food intake.

Women and food

Oxfam is helping communities establish vegetable gardens in the Highlands of Papua New Guinea. Photo: Jerry Galea
Oxfam is helping communities establish vegetable gardens in the Highlands of Papua New Guinea.
Women produce the majority of the world’s food but do so under difficult conditions.
On Sub Saharan African farms, 75% of the workforce are women, they produce 80% of the household food but they only own 1% of the land and are rarely included in the decision making (either on agricultural production or at a household level).
Research has shown that farms run by educated women show increases in yields of up to 22%. Yet two-thirds of the children denied school are girls and 64% of the world’s illiterate adults are women.
Women worldwide rarely own land: in Sub-Saharan Africa women own 1% of the land, in Brazil they own 11% and in Peru 13%. Lack of land rights means women are frequently the ones left dispossessed and uncompensated. When women do own land, their holdings are smaller than their male counterparts – between 20% and 35% on average worldwide. Such land is often marginal and thus of low productivity.
Women face discrimination in terms of access to credit, tools, training and a variety of other agricultural services. Available figures show that only 5% of extension services have been addressed to rural women, while no more than 15% of the world's extension agents are women. In Africa women receive 7% of extension services and 10% of the credit to small-scale farmers. When women do obtain credit the average value is 42% of what is granted to male farmers, and often a much higher percentage of collateral is required (collateral that women rarely have, see earlier point).

Women and increasing food prices

Women and children living in poverty will be hardest hit if global food prices continue to rise. In many countries it is women who are responsible for feeding their families and, when times are hard, it is women who go without to allow their husbands and children to eat.
Governments must act now and act together to help those already facing the crisis, to avert another global crisis and to help end hunger for the almost one billion people who go to bed hungry every day.
- See more at: http://www.oxfam.org.nz/what-we-do/issues/gender-equality/women-in-the-developing-world#sthash.FNHF12KV.dpuf

    Evolution in Environmental Monitoring and Added Value of Wireless Data Transmission

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    Evolution in Environmental Monitoring and Added Value of Wireless Data Transmission
    Increasing needs for process control, as well as the global growing environmental concerns, require companies and site operators to monitor and report a very wide variety of environmental conditions. These measurements take place within and around the industrial sites to provide accurate information to local and state regulatory departments.
    Process monitoring requires having a global overview of operational figures, machine status, and utilities use. On the environmental side, most measurements concern gaseous emissions or effluent discharge. The environmental variables that must be recorded and reported vary depending upon each industrial site and activity. Provided by all types of on-site instrumentation, sensor data may include temperature, flow, pressure, and the composition of utilities, liquid, and exhaust discharged into the environment.
    Bringing existing sites up to the new technological standards can be a time consuming and costly task because the power supply and signal wires to and from the sensors were not part of the original facility’s plan. Today’s industrial wireless technology is easy to install, power grid independent, and provides several configurations such as simple point to point, star, or tree network topologies where multiple sensors, instrumentation, and controllers can be connected over an entire plant.
    Continuous improvement in wireless technology has made monitoring process and environmental conditions in many hazardous locations much easier and safer with the development of autonomous and EX approved devices. Personnel are no longer exposed to dangerous or unpleasant environments and the frequency of manually monitoring or recording environmental readings from difficult-to-access locations has decreased.
    Banner Engineering has developed a series of industrial wireless I/O solutions that range from self-contained, environmentally rated housings to embeddable board models designed to be installed into enclosures already in use at the site.

    Environmental Monitoring Applications
    Due to the configuration of waste, water, and wastewater treatment sites where distance between equipment can be important, and local power supply is not always guaranteed, wireless technology is particularity adapted to monitoring process and environmental data. These configurations are also commonly found in the oil and gas industries.

    Water treatment plants
    Water undergoes several stages during its treatment process, from primary treatment to coagulation, flocculation, and clarification. Instrumentation and sensors are installed at several stages of the process. One sensitive point is measuring the sludge level in the clarification tank. Because the sensor is installed on the clarification tank bridge, communicating the sensor information back to the supervisor is done using slip rings that do not guarantee a reliable transmission and need frequent replacement. By using a wireless node, signals from multiple tanks can be transmitted up to several hundred meters to the main control room.

    Another common wireless application for factories or wastewater facilities is monitoring the temperature of the effluent discharge into the river and comparing it to the upstream water temperature. Although the distance from the river edge to the treatment plant is short, often there is no power at either data collection point and wiring can be cost prohibitive compared to the cost of the current wireless technology and temperature sensors.

    River and Pond Level Control
    Monitoring and controlling river, pond, and lake levels is an ideal example of using wireless technology in areas without access to wired power or data communication.
    Radar gauges, encoders, and float systems connected to wireless devices are used to monitor lake levels. The wireless devices translate the level data back to a control center for logging and analysis. Submersible pressure sensors connected to wireless devices are also used to monitor retention pond levels. Level data is transmitted back to central control rooms for analysis to prevent retention ponds from overflowing during rainstorms or releasing the runoff into streams and rivers before it is tested for contaminants.

    Landfill Leachate and
    Biogas Monitoring
    Regulatory agencies require landfill operators to measure and monitor the water levels within all ground wells in the landfill site, monitor leachate accumulation and removal, and accurately monitor methane gas production, removal, venting, and burning.
    Wireless devices connected with a counter input and submersible pressure sensor/transmitter reliably monitor both the leachate level and the pump. The submersible pressure transmitter monitors the leachate level while the pump strokes used to remove that leachate are counted. The sensor information is wirelessly transmitted to a host system that stores the data, performs calculations, or notifies personnel when a service vehicle is needed at a specific well.
    Biogas wellheads equipped with a pressure sensor and wireless EX approved wireless node send back status signals on gas production for each individual well. Negative pressure within the methane production system is monitored and adjusted in real time, increasing efficiency and cost effectiveness. Thermocouples are used on the flare to monitor flame temperature and verify that the combustion of methane is ongoing. The wireless devices connected to both a pressure transducer and the temperature sensors collect the data and wirelessly transmit the data back to a host system for logging and analysis to comply with local, state, and federal regulations.
    Anaerobic Digestion
    Biodegradable material is digested by bacteria in a special tank. Depending on regulations, the produced biogas can be injected into the distribution grid and sent to a cogeneration unit to produce electricity and heat. During the process stages, it is necessary to measure the storage tank fill level, biogas pressure in the digester, flare status, and other parameters. Battery operated DX99 wireless units can help to monitor these values from the control room without having to run new cables.

    Compost Temperature Management
    To increase the efficiency of composting and ensure proper hygienisation, the temperature of the compost piles is measured and logged constantly through wireless temperature probes equipped with three sensing points.
    Using wireless devices increases workplace safety because operators do not need to climb onto the piles several times a week to manually monitor the temperatures. Manually collecting this data is time consuming, introduces errors, and exposes the personnel to harmful pathogens.
    Automatically collecting the data using sensors and wirelessly transmitting the data back to a centralized location allows composting temperatures to be continually recorded and logged, improving efficiency and reducing the time needed to complete a composting cycle.

    Gas Detection in a
    Hazardous Environment
    In a recent application, a major French gas detection company installed gas detectors on a UK client site to ensure employee safety around the plant and detect any hazardous situation. Due to the facility’s size, running additional wires to the detectors situated far from the control room would have been complex and too expensive.
    Instead, they equipped the sensors with a wireless OEM board. With this option, the signal from all detectors can be remotely monitored at all times, effectively protecting the site personnel and limiting the need to enter potentially dangerous areas.

    Oil and Gas
    Having a precise control of tanks volumes allows operating companies to efficiently coordinate fuel purchases with respect to fuel market fluctuations. It also helps avoid losses and inaccuracies caused by human errors. The exact measure of volume is not dependent only on level; mass, temperature, and density variations have also to be taken into consideration. Installation costs for this type of application can be very high because of the tank’s remote location, which can be several hundred meters apart, as well as being in an ATEX zone. Banner Engineering’s wireless modules connected to the instrumentation will transmit the sensor signals back to the primary control location.

    Slurry Pipeline Leak Monitoring
    Coal slurry is the dirty water used to wash coal during mining. After the washing process is complete, the slurry is pumped to a slurry retention pond.
    To prevent the slurry from entering streams and local water supplies, retention ponds are usually created within valleys between hills. While the slurry is pumped from the mine site over hills into the retention pond, the flow rates are measured at the origination site and at the retention pond. Sensors are also positioned at pipeline splices to detect leaks.
    Wireless devices and flow sensors were mounted at each end of the pipeline to detect changes in the flow rates. Wireless devices and optical sensors were used at all pipeline splices to detect the presence of liquid. When a leak is detected, signals sent from the radios back to the control location shut down the slurry pumps to minimise the leaks.
    Because the total length of the pipeline can be several miles, a wireless solution eliminates the need to run power and data cables the entire length of the pipeline. The wireless devices and their sensors can also be moved if the configuration of the pipeline ever changes.


    The importance of effective leadership in improving EHS performance and to disseminate these findings to other organizations seeking to develop new or tailor existing EHS initiatives. Several important findings have emerged from this research effort:

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    The importance of effective leadership in improving EHS performance and to disseminate these findings to other organizations seeking to develop new or tailor existing EHS initiatives.
    Several important findings have emerged from this research effort:
      Leadership style Effective EHS leaders have the ability to inspire others to behave safely,
    recognize the connection between good safety and good business practices, possess up-to-date
    EHS knowledge, and have the communication skills to convey it. Furthermore, a combination of
    transactional and transformational leadership styles brings about remarkable achievements in EHS
    performance.
    Accountability Senior line management has ultimate responsibility and accountability for EHS
    policies and incidents. Effective leaders take the time to regularly relay messages of safety through various channels. Leaders also integrate EHS into performance reviews via leading and lagging indicators to demonstrate their organization’s and personal commitment to worker safety.
    Worker empowerment Worker empowerment regarding the development, distribution,
    and enforcement of EHS messages and policies is important for obtaining worker consensus and
    compliance. Equally important are leader-member exchanges and the encouragement of safety
    citizenship behavior to involve workers in safety initiatives.
    EHS and its role in business decisions EHS factors into all major business decisions,
    such as new product development, mergers, acquisitions and contractor relations.
    Leadership training Leadership training is essential to ensuring that EHS leaders are grown
    within an organization. Such training focuses on the “soft skills” of effective EHS communication in
    addition to technical safety training.
    Safety climate and culture Safety needs to be a value, not just a priority, if it is to be firmly
    embedded within an organization’s culture. It is a leader’s responsibility to recognize and celebrate safe
    behavior to emphasize the central role of EHS in the organization.


    This comparative analysis described EHS leadership as a multidimensional construct with the following key components:
    ❱ Personal commitment and accountability at the highest organizational level;
    ❱ Comprehensive leadership training of managers and executives;
    ❱ Integration of EHS into performance measurement plans using relevant metrics; and
    ❱ Worker empowerment.
     

    Interview Questions EHS DEVELOPMENT IN ORGANISATION

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    Interview Questions
    Leadership style
      What qualities or skills of your CEO make him an effective leader in EHS?
      How does your CEO visibly demonstrate his commitment to EHS within the company?
      How does your CEO set a positive example in regards to EHS?
    Accountability
      What is the highest level of leadership held accountable for EHS at your company?
      What kinds of EHS metrics are built into your leaders’ performance reviews (e.g., leading vs. lagging)?
      What methods of communication does leadership employ for making safe work practices visible to all employees throughout your organization (e.g., publications, technology, etc.)?
      What lengths has management taken to become accessible to employees in regards to safety issues and concerns?
    Worker Empowerment
    • Do you think your company employees see meaningful opportunities to be personally
    engaged in promoting safety in the workplace?
      Is employee input included in the process of developing or revising EHS policies and practices?
      Are there rewards or incentive programs that are designed to recognize frontline employees
    for their contribution to EHS?
    EHS  and its role in business decisions
      Does the C-suite get involved in the development of your company’s EHS policy?
      To what extent do you think EHS considerations inform business decisions within your company?
      What role does EHS play in business decisions (e.g., mergers and acquisitions)?
      Please describe how the organization approaches relationships between the workforce
    and management, including contractors.
    Leadership training
      Is leadership throughout your organization required to take EHS training?
      What kind of EHS training is a requirement for leadership throughout the levels of your
    organization?
      What other kinds of training are available to leadership within your organization?
    Safety climate and culture
      How does leadership inspire, build, and continue to uphold an EHS culture, nurturing positive
    behaviors and practices?
      Please explain how the management style contributes to the EHS culture at your organization.
      How does your organization assess and measure EHS culture?

    International Conference on Environment

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    with best regards,
    (2014)
    Dr. AMAR NATH GIRI
    EHSQ , NFCL
    amarnathgiri@nagarjunagroup.com
    M.Sc.,Ph.D & DIPLOMA AS - P.G.D.E.P.L,CES, DCA,
    EX IIM LUCKNOW FELLOW, EX RESEARCH SCIENTIST
    IGIDR-MUMBAI 
    EHSQ BLOG :http://dramarnathgiri.blogspot.in/?view=magazine


    ---------- Forwarded message ----------
    From: Vivek U. Glendenning “Nomad”<vivekglendenning@groundreportindia.org>
    Date: Sun, Mar 9, 2014 at 8:12 PM
    Subject: If you are interested to know more about Indian common villages and communities
    To: environment.conferences@lists.riseup.net, groundreport@googlegroups.com


    Dear Patron,
    Have a good day

    We are traveling all over India covering around 100,000 kilometres for various environment, climate change, agriculture, water and waste management issues including social environment.

    Please let us know, if you 
    - want to join the tour  or
    - know an individual or organization or group working on the above issues

    Thank you
    Regards
    Vivek 

    °°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°
    Vivek U Glendenning "Nomad" MCIJ
    http://www.nomadhermitage.groundreportindia.org

    The Chief Editor, Ground Report India Group of Journals
    http://www.groundreportindia.org

    Facebook Group-  https://www.facebook.com/groups/groundreportindia.discussion
    Facebook Page-  https://www.facebook.com/nomad.cottage

    °°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°°

    206 Conferences on Environment & Climate Change and a 1,00,000 kms national tour

    1 WHY INDIA PLAYS AN IMPORTANT ROLE IN PROTECTING THE ENVIRONMENT



    India is a vast country with a large population, amazing social diversities, social & economic biases and inequalities. India is a growing consumer economy and will one day have amongst the largest group of consumers in the world. However, the population of India must be seen beyond that of potential consumers for international markets. The Indian population must play an important role in protecting the environment. It is therefore increasingly important that work is done to create environmental awareness with the common people of India towards sustainable development. We need to explore the people, groups and organizations working for environmental issues on the real ground if we are serious about protecting the environment. Exclusive awareness and participatory dialogue programs with the common people is needed that promote decentralized methods of protecting the environment.


    However, currently in India there is little public dialogue or community awareness about the local and global issues facing the environment. What is climate change? What are other issues facing the environment? And what are roles people can play to protect the environment? In answering these questions, it is our view that environmental issues cannot be resolved only by funded academic research, or through grants and programs supported by government agencies. Environmental problems need to be resolved by and between individuals, which includes common people, the corporate sector, academics, NGOs and government. All sectors and all individuals need to consider their role in protecting the environment and work together towards a common goal.
    In order to begin to work towards sustainable development, we propose a chain of environment conferences. The most important activity of this chain of environment conferences is a dialogue with common people about their environment, its problems and potential solutions. If common people will understand how environmental issues are related to them and their future generations, then they can start to work for the environment sincerely, including advocating to government and private sector to make better policies for the environment that promote its sustainability.
    2 THE ACTIVITY
    Ground Report India (GRI) was founded as an accountable media platform. The people of GRI go to the ground for their reports. In this process they found that there is a missing gap - most people didn’t understand or were not aware about environmental issues, even though it is one of the most important issues of the world today. GRI has also published special editions on water, agriculture and tribal issues. Through this, GRI found that many common people and local communities are supporting sustainable development and could play larger roles in working to resolve environmental issues. 
    Based on this work, we have decided to initiate a sincere dialogue and awareness program for the environment in India. We plan to organize a chain of conferences. There are hundreds conferences currently going on across the globe and in India, but they do not touch the common people. This chain of conferences will not be limited to research in academic institutions. If a person, a local community, a voluntary group is doing works or making efforts for the environment on the ground then they will have the opportunity to present and speak at these conferences. Various stratums of the human systems co-related with the environment will also be participate. This includes people in urban and rural areas; the media; lawyers; local administration; research institutes; policy activists; students; local leaders; NGOs; corporate sector; central and state governments including government bureaucrats, political leaders and common leaders.
    The environment is not limited to the planting of trees, or building of water bodies. The use of natural resources depends on the community mentality, customs and social behaviours. This chain of conferences will try to understand the solution locally with relation to society as a whole.
    With the support of local people, academics, government, private sector, civil society and you, Ground Report India Group will conduct three levels of conferences over two years from July 2012 to October 2014 for mass awareness and public dialogues on environmental issues. This includes:
    • 1 international conference
    • 5 regional conferences in different states in India
    • 200 local conferences in different regions of many states across India
    • 1,00,000 kilometres exclusive national tour covering different areas of India
    • Talks, quizzes and debates in colleges, institutes and universities
    3 THE OBJECTIVES
    After the conferences, we hope that people will at least begin to think about their local environmental issues, to know about the global environmental problems and how humans impact upon it. Presently, we see that people don’t understand the important role they can personally play to protect the environment. At the moment, environmental activism in India is elite or is considered an elitist activity in the mind set of many people. People think they cannot do anything to protect the environment. But we hope that the conferences will break this and that people will recognise that protecting the environment can be done by anyone. We also recognise that in a country of such diversity as India, each individual has a different role to play, no matter which layer of society they are in and what assets they may or may not have. We also believe that environmental protection and sustainable development can have many positive impacts for people’s livelihoods and well-being. We start from the point that rather than looking only at the government to provide the answers, we also need to start how as a society we can collectively work together to resolve environmental issues. 
    Overall, through this activity we hope to:
    • Change people’s behaviour in their daily lives to have more consideration for their individual impact on the environment, as well as those in their locality. At each local and regional conference we will facilitate discussion on major environmental topics related to the local area. This could include, for example, water quality issues, energy security, waste management and air pollution.
    • Catalyse a people’s movement to advocate and work for the environment. At each local and regional conference, leaders will be identified who are passionate to continue working for environmental issues in their locality. At the international conference, organised in the year 2014, these leaders will come together to share experiences, learn from each other, and unite with others nationally and internationally.
    • Popularise environmental issues/education and catalyse environmental advocacy in India. Environmental movements are strong in western countries, for example through Al Gore’s campaign. But because of India’s poverty, population, diversity and complexity, a different awareness is needed, that allows people to improve their livelihood and well-being while also protecting their natural resources. 
    • Record and summarise the outcomes of each conference. We acknowledge that across such an amazing country like India, not all environmental issues will be the same. Different pressures exist for different resources. For example, water is too much in some places, and less in others. Mining is common in some states, while issues related to urbanisation is more relevant in some towns and cities. We aim to present findings from each local and regional conference at the international conference. We plan to channel the questions that come up at the conferences, then synthesise to achieve some key points that can be easily communicated. 
    • Invite all layers of society to discuss and debate about environmental issues in local/regional conferences. We want to see all sectors engaged in working for the environment. To encourage people to attend the conferences, the organisers will run smaller forums prior to the local/regional conferences will target specific groups of people and leaders in sectors including government, academia, education, spiritual/religious leaders, activists, lawyers and students. At the international conference, we hope that the leaders from each sector in the local/regional conferences will attend at the international conference. 
    We will work to support people, in whatever position they are in, to do as they can – we will work with them on issues that will be relevant to them and their ability. 
    4 THE METHOD 
    4.1 LOCAL CONFERENCES
    195 local conferences on environmental issues relevant to the locality will be undertaken. Each local conference will be a one day dialogue with local people from schools, universities, other institutes, villages nearby, suburban areas of the township of a particular area. The expected gathering for each local conference will be around 200-1,000 people. 

    The tour team will spend a few days in an area, covering many villages and townships, before the local conference. We will meet local youth, local public representatives, farmers, students, voluntary organisations, school teachers and government officials. This will be supported by the network of Ground Report India and partner organisations already have on the ground. From this activity, we aim to find interested and influential people who want to work for, or are already working for, environmental issues. We will explore with them how many conferences could happen or are needed in the locality. The local people will decide the day and venue and then we will all sit together. The venue will be decided by the local communities after the local tour. 

    We will talk with them about their local environmental issues (smaller scale) and try to explore ways that they could further resolve environmental issues locally (large scale issues). The local conferences will cover the issues related to water, agriculture, energy, consumerism, community health and education. The local conferences will be up to 10 to 50 villages. It will be important to talk with people about issues relevant to them, and also to balance with their economic development and livelihoods. 
    Through the local conferences, we will document what are their environmental issues. Considering the scale and number of local conferences, we anticipate a large number of environmental issues being highlighted. These important issues will be distilled and become the starting discussion point at the regional conferences and ultimately the international conference, where experts will also attend to meet and discuss with local leaders. 
    4.2 REGIONAL CONFERENCES
    The ten two-day regional conferences will start in 2014 after organizing the local conferences. Each regional conference will be a two day dialogue with an expected gathering of around 1000-5000 people.

    The tour team will spend around 40-130 days in a region of various states covering hundreds of villages and townships. The venues will be decided by the communities after the first round of the dialogue with the voluntary and social organisations. The regional conferences will be held in the states of Uttar Pradesh, Bihar, Rajasthan, Chhattisgarh, Madhya Pradesh, Nagaland and Kerala. Each regional conference will try to cover a few states. Interested and influential people will be invited to the regional conference, and many of them will be found from the local conferences. Academic institutes will also be invited. The regional conferences will reach policy makers. Documentation and follow-up to each conference will ensure that the discussions and conclusions are bought to the attention of policy makers and others. 

    The regional conferences will begin to consider ideas to support local communities to protect their environment and will cover similar issues as the local conferences including, water, agriculture, forestation, waste management and pollution. At the regional conference, discussion of the environmental issues highlighted at the local conferences will be discussed and the most important issues and how collectively the local issues could be resolved. Also, because the regional conferences will cover a greater geographic area, environmental issues will still be locally relevant, but also encompass environmental issues that are present at a larger scale and could be tackled collectively at a this scale. 
    4.3 INTERNATIONAL CONFERENCE
    A four-day international conference on the environment and climate change will take place in 2015. Experts from many countries will meet with national leaders in India over four days. This conference will occur at the end of the chain of conferences, thereby bringing all the lessons and stories learnt from the local and regional conferences, in addition to the national tour, to a culmination point at the international conference. The expected gathering will be around 5,000-15000 people. The international conference will cover the following issues: climate change; conservation; water reservoirs; energy; environment degradation; farming and agriculture; land degradation and use; waste management; health; resource depletion; water pollution; air pollution; industrial pollution; food pollution; population; consumerism. All the environmental issues from the local and regional conferences will be brought to this conference and discussed. The role of each sector and each community will be discussed to see how each can assist the other. 

    The two main aims of the international conference are to:
    • Link the network of people working in the environment, with the hope that it could join India’s local environmental leaders with international campaigns/movements for environmental and climate change. At the international conference, the ground environmental leaders and genuine interested people will be introduced to the international community – that is people who are really interested in environmental issues and have been working for it. Because the Indian population is very large thus it could play a larger role in global environmental movements. The international conference will provide an opportunity to explore how this could be done. The local conferences, regional conferences and 100,000 kilometres exclusive national tour will build a ground network in thousands of villages, sub-urban and urban areas for the international environment movements.
    • Discuss the recorded documentation of environmental problems and issues from the local and regional conferences. Through this activity we hope that participants will begin to see the important role of each individual and organisation in working to assist local communities across the nation to solve the identified environmental issues. 
    4.4 THE TOUR 
    To make this chain of conferences worthwhile and down to earth, which means that it will cover various stratums of the human made systems with the best involvement of common people, we will conduct a 100,000 km national tour and talks, quizzes and debates in thousands of colleges, institutes and universities consecutively as the conferences. Through the national tour, talks, quizzes, debates and local conferences, we will connect with the common people. Through connecting with local people during the national tour, we will hold the local, regional and international conferences. The local conferences will be organic – they will occur as the local people suggest.
    A 100,000 kilometres national tour will be done for participatory dialogues covering thousands of villages, townships and metro-cities in next around two years. The tour will be in two parts, whereby 50,000 kms will be an exclusive national tour covering all over India, and the second 50,000 kms will be the chain of various local and regional tours supporting local and regional conferences. 
    4.5 Talks, quizzes and debates in colleges, institutes and universities:
    Talks, quizzes and debates based on environment issues in thousands of colleges, institutes and universities will be organized on the national tour. Awards, lucky draws and certificates will be given to the students at local level and at international conference.
    **************************************************
    The International Advisory Board:
    **************************************************
    Idea Initiator:
    Credits for the concept note:
    • Vivek Umrao Glendenning "Nomad's Hermitage"
    • Prof. Willem Vervoort, PhD, University of Sydney, Australia
    • John Szemerey, Belgium
    • Dr Madeleine Florin, PhD, Wageningen University, Netherlands
    • Dr Madan Thangavelu, PhD, University of Cambridge, U.K.
    • Dr B. K. Sharma, U.K.
    • Shankar Sharma, India







    Factors Affecting DO

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    Factors Affecting DO
    • Volume and velocity of water flowing in the water body

    In fast-moving streams, rushing water is aerated by bubbles as it churns over rocks and falls down hundreds of tiny waterfalls. These streams, if unpolluted, are usually saturated with oxygen. In slow, stagnant waters, oxygen only enters the top layer of water, and deeper water is often low in DO concentration due to decomposition of organic matter by bacteria that live on or near the bottom of the reservoir.
    Dams slow water down, and therefore can affect the DO concentration of water downstream. If water is released from the top of the reservoir, it can be warmer because the dam has slowed the water, giving it more time to warm up and lose oxygen. If dams release water from the bottom of a reservoir, this water will be cooler, but may be low in DO due to decomposition of organic matter by bacteria.

    • Climate/Season
    The colder the water, the more oxygen can be dissolved in the water. Therefore, DO concentrations at one location are usually higher in the winter than in the summer. During dry seasons, water levels decrease and the flow rate of a river slows down. As the water moves slower, it mixes less with the air, and the DO concentration decreases. During rainy seasons, oxygen concentrations tend to be higher because the rain interacts with oxygen in the air as it falls. More sunlight and warmer temperatures also bring increased activity levels in plant and animal life; depending on what organisms are present, this may increase or decrease the DO concentration.
    • The type and number of organisms in the water body
    During photosynthesis, plants release oxygen into the water. During respiration, plants remove oxygen from the water. Bacteria and fungi use oxygen as they decompose dead organic matter in the stream. The type of organisms present (plant, bacteria, fungi) affect the DO concentration in a water body. If many plants are present, the water can be supersaturated with DO during the day, as photosynthesis occurs. Concentrations of oxygen can decrease significantly during the night, due to respiration. DO concentrations are usually highest in the late afternoon, because photosynthesis has been occurring all day. For an example of how DO can vary from day to night.

    • Altitude
    Oxygen is more easily dissolved into water at low altitudes than at high altitudes, because of higher atmospheric pressure.
    • Dissolved or suspended solids

    Oxygen is more easily dissolved into water with low levels of dissolved or suspended solids. Waters with high amounts of salt, such as the ocean (which contains about 35 grams of salt for each 1000 grams of water) have low concentrations of DO. Freshwater lakes, streams, and tap water generally contain much less salt, so DO concentrations are higher. As the amount of salt in any body of water increases, the amount of dissolved oxygen decreases. An increase in salt concentration due to evaporation of water from an ecosystem tends to reduce the dissolved oxygen available to the ecosystem’s inhabitants. Runoff from roads and other paved surfaces can bring salts and sediments into stream water, increasing the dissolved and suspended solids in the water.
    • Amount of nutrients in the water

    Nutrients are food for algae, and water with high amounts of nutrients can produce algae in large quantities. When these algae die, bacteria decompose them, and use up oxygen. This process is called eutrophication. DO concentrations can drop too low for fish to breathe, leading to fish kills. However, nutrients can also lead to increased plant growth. This can lead to high DO concentrations during the day as photosynthesis occurs, and low DO concentrations during the night when photosynthesis stops and plants and animals use the oxygen during respiration. For an example of how DO can vary from day to night, select here.
    Nitrate and phosphate are nutrients. Nitrate is found in sewage discharge, fertilizer runoff, and leakage from septic systems. Phosphate is found in fertilizer and some detergents. 
    • Organic Wastes

    Organic wastes are the remains of any living or once-living organism. Organic wastes that can enter a body of water include leaves, grass clippings, dead plants or animals, animal droppings, and sewage. Organic waste is decomposed by bacteria; these bacteria remove dissolved oxygen from the water when they breathe. If more food (organic waste) is available for the bacteria, more bacteria will grow and use oxygen, and the DO concentration will drop.
    Directly downstream from where sewage effluent is discharged to a river, DO content often decreases, because of the increase in growth rate of bacteria that consume the organic matter contained in the effluent. The degree and extent of the DO "sag" depends on the Biological Oxygen Demand (BOD) of the effluent (how much oxygen the effluent can consume) (Giller and Malmqvist, 1998).
    • Riparian Vegetation

    Shading tends to lower average summer temperature and reduce the daily duration of higher temperature. Removing trees reduces shade on the creek, allowing the sun to warm the water. This can affect DO concentrations in different ways. As mentioned above, in general, as water temperature increases, DO drops. Also, the bare soil exposed from removing the tree can erode, increasing the amount of dissolved and suspended solids in the water. This also leads to a decrease in DO concentrations. However, direct sunlight, along with increased nutrients can increase the growth rate of aquatic plants. These plants release oxygen to the water during the day, but then remove oxygen from the water at night. This can cause DO concentrations to become very high during the day, then very low during the night. For an example of how DO can vary from day to night, select here .
    • Groundwater Inflow

    The amount of groundwater entering a river or stream can influence oxygen levels. Groundwater usually has low concentrations of DO, but it is also often colder than stream water. Therefore, groundwater may at first lower the DO concentration, but as groundwater cools the stream or river, the ability of the water to hold oxygen improves.

    Why are Nitrogen Concentrations an indicator of Water Quality?

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    Why are Nitrogen Concentrations an indicator of Water Quality?

    Abnormal levels of Nitrogenous Compounds generally indicates pollution. Most of the nitrogen found in water originates from the decay from the remains of plants and animals. Ammonia Nitrogen is the most common form of nitrogen from an effluent involving the biological breakdown of animal waste products. Since it is readily oxidizes to either nitrite or nitrate under aerobic conditions, high amounts of this pollutant may indicate a fairly fresh or recent pollution event. Although to a lesser extent than nitrate-nitrogen, ammonia can be utilized by aquatic plants and algae to support their growth. Examples of sources of this type of nitrogen would be from wastewater treatment plants, failing septic tank systems, and runoff from livestock farms. When dissolved oxygen is readily available, bacteria quickly oxidize ammonia to nitrate through a process known as nitrification. Other types of bacteria produce ammonia as they decompose dead plant and animal matter. Depending on temperature and pH (a measurement of “acidity”), high levels of ammonia can be toxic to aquatic life. High pH and warmer temperatures increase the toxicity of a given ammonia concentration. High ammonia concentrations can stimulate excessive aquatic production and indicate pollution. Important sources of ammonia to lakes and streams can include: fertilizers, human and animal wastes, and by-products from industrial manufacturing processes. Techniques to prevent high ammonia concentrations involve filtration of runoff water especially from barnyards and other areas where animals may be kept in larger numbers, proper septic system maintenance, and not over-fertilizing yards or fields.
    In order to understand and remove nitrogen when it threatens the stability of your water source, you must understand the different forms of nitrgen and some commonly referred to terms that you will be dealing with.    
      • Total Nitrogen is the sum of all nitrogen forms (TKN + NO2 + NO3)
      • Total Kjeldhal Nitrogen (TKN); this is the sum of NH3 + Organic Nitrogen
      • Ammonia Nitrogen (NH3)
      • Nitrite (NO2)
      • Nitrate(NO3)
      • Nitrogen Gas (N2)
      • Refractory Nitrogen is the Nitrogen that is not biologically decomposable
    Each of these nitrogen components play a role in the overall nitrogen manifestation in water quality. For example, for every 1 part ammonia(NH3) converted to nitrate (NO3) - 7.1 parts of alkalinity are depleted, and for every 1 part nitrate (NO3) removed - 3.6 parts alkalinity are recovered.  
       
    How do Nitrogen Concentrations affect Water Quality?


    Nitrogen-containing compounds act as nutrients in streams, rivers, and reservoirs. The major routes of entry of nitrogen into bodies of water are municipal and industrial wastewater, septic tanks, feed lot discharges, animal wastes (including birds and fish), runoff from fertilized agricultural field and lawns and discharges from car exhausts. Bacteria in water quickly convert nitrites [NO2-] to nitrates [NO 3 -] and this process uses up oxygen. Excessive concentrations of nitrites can produce a serious condition in fish called "brown blood disease." Nitrites also can react directly with hemoglobin in the blood of humans and other warm-blooded animals to produce methemoglobin. Methemoglobin destroys the ability of red blood cells to transport oxygen. This condition is especially serious in babies under three months of age. It causes a condition known as methemoglobinemia or "blue baby" disease. Water with nitrate levels exceeding 1.0 mg/L should not be used for feeding babies. High nitrates in drinking water can cause digestive disturbances in people. Nitrite/nitrogen levels below 90 mg/L and nitrate levels below 0.5 mg/L seem to have no affect on warm water fish. Because nitrogen is such an involved chemical, its consequences exceed simply water quality and extend to their consequences to organisms.
    What level of Nitrogenous Compounds is preferable for a sustainable community?

    On one hand, you do not want nitrogenous compounds to rise too high.  Monitoring studies conducted at national and state levels show that nitrogen (N) concentrations in groundwater exceed health standards more often than other common contaminants, such as pesticides. A nationwide survey conducted by EPA showed that 1.2 percent of community and 2.4 percent of private drinking water wells exceeded the 10 parts per million (ppm) nitrate-nitrogen (NO3-N) standard. Though it rarely occurs, you also do not want nitrogen to drop too low. Nitrogen-containing compounds act as nutrients in streams, rivers, and reservoirs. Nitrite/nitrogen levels below 90 mg/L and nitrate levels below 0.5 mg/L seem to have no affect on warm water fish.

    Why are Nitrates and Nitrites indicators of sustainability?

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    Why are Nitrates and Nitrites indicators of sustainability?
    Nitrate and nitrite are compounds that contain a nitrogen atom joined to oxygen atoms, with nitrate containing three oxygen atoms and nitrite containing two. In nature, nitrates are readily converted to nitrites and vice versa. Both are anions, or ions with a negative charge. They tend to associate with cations, or ions with a positive charge, to achieve a neutral charge balance.Nitrates are naturally present in soil, water, and food. In the natural nitrogen cycle, bacteria convert nitrogen to nitrate, which is taken up by plants and incorporated into tissues. Animals that eat plants use the nitrate to produce proteins. Nitrate is returned to the environment in animal feces, as well as through microbial degradation of plants and animals after they die. Microorganisms can convert nitrate or the ammonium ion (which is a nitrogen atom combined with four hydrogen atoms) to nitrite; this reaction occurs in the environment as well as within the digestive tract of humans and other animals. After bacteria
    convert (reduce) nitrate to nitrite in the environment, the nitrogen cycle is completed when they then convert the nitrite to nitrogen. Normally, this natural cycling process does not allow excessive amounts of nitrates or nitrites to accumulate in the environment. However, human activities have increased environmental nitrate concentrations, with agriculture being the major source. This includes increased use of nitrogen-containing fertilizers as well as concentrated livestock and poultry farming; the latter two produce millions of tons of nitrate-containing manure each year. Nitrate and nitrite compounds are very soluble in water and quite mobile in the environment. They have a high potential for entering surface water when it rains, as nitrates in applied fertilizers can dissolve in runoff that flows into streams or lakes; they also have a high potential for entering groundwater through leaching. The concentration associated with soil particles has been estimated to be about half the concentration in interstitial water (the water in the pore spaces between the soil particles).
    What are some health effects of Nitrates and Nitrite?
    Nitrates themselves are relatively nontoxic. However, when swallowed, they are converted to nitrites that can react with hemoglobin in the blood, oxidizing its divalent iron to the trivalent form and creating methemoglobin. This methemoglobin cannot bind oxygen, which decreases the capacity of the blood to transport oxygen so less oxygen is transported from the lungs to the body tissues, thus causing a condition known as methemoglobinemia. Normal individuals have low levels (0.5 to 2%) of methemoglobin in their blood. When this level increases to 10%, the skin and lips can take on a bluish tinge (cyanosis), and levels above 25% can cause weakness and a rapid pulse. At levels above 50 to 60%, a person can lose consciousness, go into a coma, and die. Infants are much more sensitive than adults to nitrates/nitrites, and essentially all deaths from nitrate/nitrite poisoning have been in infants. Long-term exposure to lower levels of nitrates and nitrites can cause diuresis (an increase in the amount of urine, and starchy deposits and hemorrhaging of the spleen).

    Top 10 Amazing Extinct Animals

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    Top 10 Amazing Extinct Animals

    The terrestrial fauna has undergone major changes over the millions and hundreds of years that have passed. Today, images found on the internet, images that place us in front of the weirdest and most interesting animals that have become extinct, astonish us. The next 10 animals are the statement of the miracles nature can give.
    10. The Steller Sea Cow


    This giant mammal bears the name of its finder, Georg Steller, the researcher who first saw it in the waters of Commander Islands. With a length going to 8-9 meters and a weight between 8 and 10 tons, the Steller Sea Cow was the giant from the depths. The black and thick skin, the small head and the toothless mouth gives it the image of a scary but friendly giant. The last specimen died in 1768, and in this way, the science has lost one subject of research.
    9. The Cave Lion


    This Eurasian lion, specially known for its way of living in caves, was one of the biggest predators hunting thousands years ago. The dimensions of this mammal were impressive, having the shoulder height of 1.2 meters and the length around 2 meters. It is believed to have been extinct around 10,000 years ago, once with the Würm glaciations, but it seems to have been seen around 2000 ago, in the Balkans Mountains.
    8. The Great Auk


    This amazing flightless bird succeeded in carrying its existence till more recent times, 1844 being the year of the last recording of its presence. The features were the same with the today’s penguins, having white and black feathers. The Great Auk was measuring around 75 centimeters high and was weighing up to 5 kilograms. Today, this population has been extinct, and the lands of Canada, Iceland, Greenland, Norway or Great Britain lack this amazing and interesting creature.
    7. Dodo bird


    Flightless and very much similar to the mixture between pigeons and doves, this Mauritian specific bird has been considered the archetype of the extinct species. Having a meter tall, its presence wasn’t hard to miss, and people are the main responsible for its extinction. Beginning with the 17th century, the phrase “as dead as a dodo” is synonymous with undoubted death.
    6. The Aurochs

    250,000 years ago represents the starting point of the existence of this amazing animal on the European continent. And due to its huge importance as a prize, its hunting was allowed only to nobles and the members of the royal court. As the aurochs populations were reducing, the royal court decided to ask for the services of the gamekeepers. In spite of all the measures taken, the last aurochs female died in 1627.
    5. The Caspian Tiger


    This amazing feline, mostly met in the western part of the Asian continent was the third in the top of the largest tigers. Its physical construction was frightening at a first look. The paws of this giant were wide and big, and the claws unusually large. You can easily compare it with the Bengal tiger in terms of colors. The weight was also impressive, the male weighing around 169-240 kilograms, and the female between 86-135 kilograms. Although extinct from 1970, few voices still claim possible apparitions of this ferocious animal.
    4. The Irish Deer


    With no less than 2.10 meters high and a distance of 3.6 meters between antlers, the Irish Elk, as the Irish population was naming it, remains the largest deer ever. More than the large and imposing body, the Irish Deer was hunted for its antlers. The last deer seems to have lived about 7,000 years ago, information given by the fossils found. This prehistoric wonder of the nature remembers us daily the things that we miscalculate when it comes to live in great communion with the surroundings.
    3. The Tasmanian tiger


    Member of the Thylacine order, the Tasmanian tiger was a totally carnivorous and the largest marsupial of those times. The last record of the Tasmanian tiger dates back to 1936, although have been recorded sightings of this creepy animal. Again, guilty of its extinction are people. Because of the massive and continuous hunting, the populations of the Tasmanian tiger reduced until extinction. Other factors could be the diseases, the hunting dogs specially trained for killing these specimens.
    2. The Quagga


    The wonders of the African continent bring us another rarity. Due to its peculiarities, Quagga, although extinct species, still raises interest from the past of the researchers. Half zebra, half horse, this amazing animal could never be classified after a certain rule. This was due to the fact that you couldn’t see two Quagga alike. Again, the hunt for meat and hides caused the extinction of this beautiful animal.
    1. The One and Only T-Rex

    On the top of the list of extinct animals is to be found the biggest and the most fearful of all times: the T-Rex. Its dimensions were stunning, 43.3 feet long and 16.6 ft tall. The weight was also unbelievable: up to 7 tons. The natural causes determined the complete extinction of this huge carnivorous 65 million years ago. With more than 30 species, the T-Rex remains the king of the fauna and the absolute master of the times.

    Industrial Dust, Air Pollution and related Occupational Diseases – Nuisance to be controlled for improvement of general environment, safety and health standard:

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    Industrial Dust, Air Pollution and related Occupational Diseases – Nuisance to be controlled for improvement of general environment, safety and health standard:

    1.0. Introduction - Air pollution is the presence of high concentration of contamination, dust, smokes etc., in the general body of air man breaths. Dust is defined as particulate matter as “any airborne finely divided solid or liquid material with a diameter smaller than 100 micrometers.” Dust and smoke are the two major components of particulate matter. Car emissions, chemicals from factories, dust, pollen and mold spores may be suspended as particles. Ozone, a gas, is a major part of air pollution in cities. When ozone forms air pollution, it’s also called smog. These materials come from various sources, such as, various industrial processes, paved and unpaved roadways, construction and demolition sites, parking lots, storage piles, handling and transfer of materials, and open areas. Some air pollutants are poisonous. Inhaling them can increase the chances of health problems. In fact, dust when inhaled can increase breathing problems, damage lung tissue, and aggravate existing health problems. In addition to health concerns, dust generated from various activities can reduce visibility, resulting in accidents. Therefore, every federal Govt. has stringent regulations which require prevention, reduction and/or mitigation of dust emissions.PDS_AIR_POLLUTION_0
    Thus, prime sources of air pollution are the industrial activities or processes releasing large quantity of pollutants in the atmosphere. These pollutants are mainly:
    (a) Smoke comes out from various industries like, power plants, chemical plants, other manufacturing facilities, motor vehicles, etc.;
    (b) Burning of wood, coal in furnaces and incinerators;
    (c) Gaseous pollutants from Oil refining industries;
    (d) Dust generated and thrown to general atmosphere by various industries such as cement plants, ore / stone crushing units, mining industries due to rock drilling & movements of mining machineries & blasting etc.;
    (e) Waste deposition for landfills which generate methane;
    (f) Toxic / germ / noxious gasses and fumes generated from military activities and explosives blasting in mines.

    2.0. Mechanism of Adverse Impact of Smoke Pollutant – The main sources of smoke pollutants in urban areas are Petrol / Diesel driven motor vehicles, Fuel combustion in stationary sources including residential, commercial and industrial heating / cooling system and coal-burning power plants etc. PDS_AIR_POLLUTION_1
    Petrol / Diesel driven motor vehicles produce high levels of Carbon Dioxide (CO2) / Carbon Monoxide (CO), major source of Hydrocarbon (HC) and Nitrogen oxides (NOx). Fuel combustion in stationary sources is the dominant source of Carbon Dioxide (CO2) and Sulfur Dioxide (SO2).
    Carbon Dioxide (CO2)– This is one of the major gas pollutants in the atmosphere. Major sources of CO2 are due to burning of fossil fuels and deforestation. Industrially developed countries like USA, Russia etc., account for more than 65% of CO2 emission. Less developed countries with 80% of world’s population responsible for about 35% of CO2 emission. Due to high growth reported from less developed countries in last decade, it is estimated that, the Carbon dioxide emissions may rise from these areas and by 2020 their contribution may become 50%. It has also been seen that, Carbon dioxide emissions are rising by 4% annually.
    As ocean water contain about 60 times more CO2 than atmosphere; CO2 released by the industry leads to disturbance of equilibrium of concentration of CO2 in the system. In such a scenario, the oceans would absorb more and more CO2 and atmosphere would also remain excess of CO2. As water warms, ocean’s ability to absorb CO2 is reduced. CO2 is a good transmitter of sunlight, but partially restricts infrared radiation going back from the earth into space. This produces the so-called “Greenhouse Effect” that prevents a drastic cooling of the Earth during the night. This so-called “Greenhouse Effect” is responsible for GLOBAL WARMING. Currently Carbon Dioxide is responsible for major portion of the global warming trend.
    Nitrogen oxides (NOx)– They come mainly from nitrogen based fertilizers, deforestation, and biomass burning. Nitrogen oxides contribute mostly as atmospheric contaminants. These gases are responsible in the formation of both acid precipitation and photochemical smog and causes nitrogen loading. These gases have a role in reducing stratospheric ozone.
    Sulfur Dioxide (SO2)– Sulfur dioxide is produced by combustion of sulfur-containing fuels, such as coal and fuel oils. SO2 also produced in the process of producing Sulfuric Acid and in metallurgical process involving ores that contain sulfur. Sulfur oxides can injure man, plants and materials. As emissions of sulfur dioxide and nitric oxide from stationary sources are transported long distances by winds, they form secondary pollutants such as nitrogen dioxide, nitric acid vapor, and droplets containing solutions of sulfuric acid, sulfate, and nitrate salts. These chemicals descend to the earth’s surface in wet form as rain or snow and in dry form as a gases fog, dew, or solid particles. This is known as acid deposition or acid rain.
    Choloroflurocarbons (CFCs)– Chlorofluorocarbons, also known as Freons, are greenhouse gases that contribute to global warming. CFCs are responsible for lowering the average concentration of ozone in the stratosphere.
    Smog – Smog is the result from the irradiation by sunlight of hydrocarbons caused primarily by unburned gasoline emitted by automobiles and other combustion sources. Smog is created by burning coal and heavy oil that contain mostly sulfur impurities.
    [For more refer Pollution from Motor Vehicles ]

    3.0. Mechanism of air pollution by particulate matters (Fine and Coarse Dust particles) – ‘Fine particles’ are less than 2.5 micron in size and require electron microscope for detection, however, they are much larger than the molecules of Ozone etc., and other gaseous pollutants, which are thousands times smaller and cannot be seen through even electron microscope.
    Fine particles are formed by the condensation of molecules into solid or liquid droplets, whereas larger particles are mostly formed by mechanical breakdown of material or crushing of minerals. ‘Coarse particles’ are between 2.5 to 10 micron size, and cannot penetrate as readily as of Fine particle; however, it has been seen these are responsible for serious health hazards. The severity of the health hazards vary with the chemical nature of the particles.
    The inhalation of particles has been linked with illness and deaths from heart and lung disease as a result of both short- and long-term exposures. People with heart and lung disease may experience chest pain, shortness of breath, fatigue etc., when exposed to particulate-matter pollutants. Inhalation of particulate matter can increase susceptibility to respiratory infections such as Asthma, Chronic Bronchitis. The general medical term given for such lung diseases is ‘Pneumoconiosis’.
    Emissions from diesel-fuel combustion in vehicles / engines / equipments; Dusts from cement plants, power plants, chemical plants, mines are a special problem, specially for those individuals breathing in close proximity to such atmosphere. Cars, trucks and off-road engines emit more than half a million tones of diesel particulate matter per year.
    3.1. Controlling Airborne Particulate Matters – Airborne particulate matters (PM) emissions can be minimized by pollution prevention and emission control measures. Prevention, which is frequently more cost-effective than control, should be emphasized. Special attention should be given to mitigate the effects, where toxics associated with particulate emissions may pose a significant environmental risk.
    Measures such as improved process design, operation, maintenance, housekeeping, and other management practices can reduce emissions. By improving combustion efficiency in Diesel engines, generation of particulate matters can be significantly reduced. Proper fuel-firing practices and combustion zone configuration, along with an adequate amount of excess air, can achieve lower PICs (products of incomplete combustion). Few following steps should be adhered to control PM:
    a. Choosing cleaner fuels – Natural gas used as fuel emits negligible amounts of particulate matter.
    b. Low-ash fossil fuels contain less noncombustible, ash-forming mineral matter and thus generate lower levels of particulate emissions.
    c. Reduction of ash by coal cleaning reduces the generation of ash and Particulate Matter (PM) emissions by up to 40%.
    d. The use of more efficient technologies or process changes can reduce PIC emissions.
    e. Advanced coal combustion technologies such as coal gasification and fluidized-bed combustion are examples of cleaner processes that may lower PICs by approximately 10%.
    f. A variety of particulate removal technologies, are available – these are (a) Inertial or impingement separators, (b) Electrostatic precipitators (ESPs) , (c) Filters and dust collectors (baghouses), (d) Wet scrubbers that rely on a liquid spray to remove dust particles from a gas stream.
    4.0. Dust in cement industry – Its prevention and collection enhances environment standard : The manufacturing of cement involves mining; crushing and grinding of raw materials (mostly limestone and clay); calcinating the material in rotary kiln; cooling the resulting clinker; mixing the clinker with Gypsum; and milling, storing and bagging the finished cement. The cement manufacturing process generates lot of dust, which is captured and recycled to the process. Gasses from clinker cooler are used as secondary combustion air. The process, using pre-heaters and pre-calciners, is both economically and environmentally preferable to wet process because of techno-economic advantages of the energy saving dry system over wet. Certain other solids such as pulverized fly ash from power plants, slag, roasted pyrite residue and foundry sand can be used as additives to prepare blended cement. pds_diagram_cement_plant
    a. Dust generation: Generation of fine particulates and dust are inherent in the process; but most are recovered and recycled. The sources of dust emission include clinker cooler, crushers, grinders and material-handling equipments. Material-handling operations such as conveyors result in fugitive dust emission.
    b. Prevention and control of dust: The priority in the cement industry is to minimize the increase in ambient particulate levels by reducing the mass load emitted from the stacks, from fugitive emissions, and from other sources. Collection and recycling of dust in the kiln gases in required to improve the efficiency of the operation and to reduce atmospheric emissions. Units that are well designed, well operated, and well maintained can normally achieve generation of less than 0.2 kilograms of dust per metric tonne (kg /t) of clinker, using dust recovery systems. For control of fugitive dust (a) ventilation systems should be used in conjunction with hoods and enclosures covering transfer points and conveyors; (b) Drop distances should be minimized by the use of adjustable conveyors; (c) Dusty areas such as roads should be wetted down to reduce dust generation; (d) Appropriate stormwater and runoff control systems should be provided to minimize the quantities of suspended material carried off site.
    c. Mechanical systems for controlling dust:Several mechanical equipments are used in cement manufacturing plant to control / collect dust. These are:
    (i) Dust collector - A dust collector (bag house) is a typically low strength enclosure that separates dust from a gas stream by passing the gas through a media filter. The dust is collected on either the inside or the outside of the filter. A pulse of air or mechanical vibration removes the layer of dust from the filter. This type of filter is typically efficient when particle sizes are in the 0.01 to 20 micron range. pds_dust_collector
    pds_cyclone(ii) Cyclone - Dust laden gas enters the chamber from a tangential direction at the outer wall of the device, forming a vortex as it swirls within the chamber. The larger articulates, because of their greater inertia, move outward and are forced against the chamber wall. Slowed by friction with the wall surface, they then slide down the wall into a conical dust hopper at the bottom of the cyclone. The cleaned air swirls upward in a narrower spiral through an inner cylinder and emerges from an outlet at the top. Accumulated particulate dust is deposited into a hopper, dust bin or screw conveyor at the base of the collector. Cyclones are typically used as pre-cleaners and are followed by more efficient air-cleaning equipment such as electrostatic precipitators and bag houses.
    pds_electrostatic_precipitator(iii) Electrostatic Precipitator - In an electrostatic precipitator, particles suspended in the air stream are given an electric charge as they enter the unit and are then removed by the influence of an electric field. A high DC voltage (as much as 100,000 volts) is applied to the discharge electrodes to charge the particles, which then are attracted to oppositely charged collection electrodes, on which they become trapped. An electrostatic precipitator can remove particulates as small as 1 μm (0.00004 inch) with an efficiency exceeding 99 percent.

    5.0. Dust in Coal Handling Plant (CHP) and its control systems: Thermal power plants (coal-fired power plants) use coal as their fuel. To handle the coal, each power station is equipped with a coal handling plant. The coal has to be sized, processed, and handled which should be done effectively and efficiently. The major factor which reduces the staff efficiency in operation of coal handling plant is the working environment i.e. a dusty atmosphere and condition. Lots of care is always needed to reduce dust emission. In developing countries, all most all systems used in power station coal handling plants are wet dust suppression systems.
    5.1. After dust is formed, control systems are used to reduce dust emissions. Although installing a dust control system does not assure total prevention of dust emissions, a well-designed dust control system can protect workers and often provide other benefits, such as (a) Preventing or reducing risk of dust explosion or fire; (b) Increasing visibility and reducing probability of accidents; (c) Preventing unpleasant odors; (d) Reducing cleanup and maintenance costs; (e) Reducing equipment wear, especially for components such as bearings and pulleys on which fine dust can cause a “grinding” effect and increase wear or abrasion rates; (f) Increasing worker morale and productivity; (f) Assuring continuous compliance with existing health regulations. In addition, proper planning, design, installation, operation, and maintenance are essential for an efficient, cost-effective, and reliable dust control system.
    5.2. There are two basic types of dust control systems currently used in minerals processing operations are:
    (a) Dust collection system - Dust collection systems use ventilation principles to capture the dust-filled air-stream and carry it away from the source through ductwork to the collector. A typical dust collection system consists of four major components, such as (1) An exhaust hood to capture dust emissions at the source; (2) Ductwork to transport the captured dust to a dust collector; (3) A dust collector to remove the dust from the air; (4) A fan and motor to provide the necessary exhaust volume and energy.
    (b) Wet dust suppression system - Wet dust suppression techniques use water sprays to wet the material so that it generates less dust. There are two different types of wet dust suppression: pds_dust_suppression
    (i) wets the dust before it is airborne (surface wetting) and
    (ii) wets the dust after it becomes airborne. In many cases surfactants or chemical foams are often added to the water into these systems in order to improve performance.
    A water spray with surfactant means that a surfactant has been added to the water in order to lower the surface tension of the water droplets and allow these droplets to spread further over the material and also to allow deeper penetration into the material.
    i. Surface wetting system: The principle behind surface wetting is the idea that dust will not even be given a chance to form and become airborne. With this method, effective wetting of the material can take place by static spreading (wetting material while it is stationary) and dynamic spreading (wetting material while it is moving). For static wetting, more effective dust suppression arises by increasing the surface coverage by either reducing the droplet diameter or its contact angle. For dynamic spreading, more factors come into play such as the surface tension of the liquid, the droplet diameter, the size of the material being suppressed, and the droplet impact velocity.
    airborne_dust_1ii. Airborne dust capture system - Airborne dust capture systems may also use a water-spray technique; however, airborne dust particles are sprayed with atomized water. When the dust particles collide with the water droplets, agglomerates are formed.  These agglomerates become too heavy to remain airborne and settle. Airborne dust wet suppression systems work on the principle of spraying very small water droplets into airborne dust. When the small droplets collide with the airborne dust particles, they stick to each other and fall out of the air to the ground. Research showed that, if a sufficient number of water droplets of approximately the same size as the dust particles could be produced, the possibility of collision between the two would be extremely high. It was also determined that if the droplet exceeded the size of the dust particle, there was little probability of impact and the desired precipitation. Instead, the dust particle would move around the droplet.
    5.3. System Efficiency: Over the years, water sprays has established the following facts:
    (a) For a given spray nozzle, the collection efficiency for small dust particles increases as the pressure increases;
    (b) At a given pressure, the efficiency increases as the nozzle design is changed so as to produce smaller droplets. The efficiency of spray dust capture increases by increasing the number of smaller sized spray droplets per unit volume of water utilized and by optimizing the energy transfer of spray droplets with the dust-laden air.
    5.4. Sophisticated system like ‘Ultrasonic Dust Suppression’ systems uses water and compressed air to produce micron sized droplets that are able to suppress respirable dust without adding any detectable moisture to the process. Ideal for spray curtains to contain dust within hoppers. The advantages of using Ultrasonic Atomizing Systems for dust suppression can therefore be summarized as: (a) reduced health hazards; (b) decrease in atmospheric pollution; (c) improved working conditions; (d) efficient operation with minimum use of water.

    6.0. Air pollution control devices / equipments for industries, in general – The commonly used equipments / process for control of dust in various industries are (a) Mechanical dust collectors in the form of dust cyclones; (b) Electrostatic precipitators – both dry and wet system; (c) particulate scrubbers; (d) Water sprayer at dust generation points; (e) proper ventilation system and (f) various monitoring devices to know the concentration of dust in general body of air.
    The common equipments / process used for control of toxic / flue gases are the (a) process of desulphurisation; (b) process of denitrification; (c) Gas conditioning etc. and (d) various monitoring devices to know the efficacy of the systems used.
    7.0. Occupational Hazards / diseases due to expose in dusty and polluted air: There are certain diseases which are related to one’s occupation. These are caused by constant use of certain substances that sneak into air and then enter our body.
    (i) Silicosis (Silico-tuberculosis) occurs due to inhalation of free silica, or SiO2 (Silicon dioxide), while mining or working in industries related to pottery, ceramic, glass, building and construction work. The workers get chronic cough and pain in the chest. Silicosis treatment is extremely limited considering a lack of cure for the disease. However, like all occupational respiratory ailments, it is 100% preventable if exposure is minimized.
    (ii) Asbestosis is caused by asbestos, which is used in making ceilings. It is also considered as cancer causing agent. Pathogenesis of the disease is characterized as progressive and irreversible, leading to subsequent respiratory disability. In severe cases, asbestosis results in death from pulmonary hypertension and cardiac failure.
    (iii) Byssinosis, also referred to as brown lung disease, is an occupational respiratory disorder characterized by the narrowing of pulmonary airways. It is a disabling lung disease, which is marked by chronic cough and chronic bronchitis due to inhalation of cotton fibers over a long period of time.
    (iv) Coal worker’s Pneumoconiosis occurs due to inhalation of coal dust from coal mining industry. Also referred to as black lung disease. The workers suffer from lung problems. Apart from asbestosis, black lung disease is the most frequently occurring type of pneumoconiosis . In terms of disease pathogenesis, a time delay of nearly a decade or more occurs between exposure and disease onset.
    7.1. Preventive Measures – The most successful tool of prevention of respiratory diseases from industrial dust is to minimize exposure. However, this is not a practical approach from the perspective of industries such as mining, construction/demolition, refining/manufacturing/processing, where industrial dust is an unavoidable byproduct. In such cases, industries must implement a stringent safety protocol that effectively curtails exposure to potentially hazardous dust sources. National Institute for Occupational Safety and Health (NIOSH) recommended precautionary measures to reduce exposure to a variety of industrial dust types.
    1.    Recognize when industrial dust may be generated and plan ahead to eliminate or control the dust at the source. Awareness and planning are keys to prevention of silicosis.
    2.    Do not use silica sand or other substances containing more than 1% crystalline silica as abrasive blasting materials. Substitute less hazardous materials.
    3.    Use engineering controls and containment methods such as blast-cleaning machines and cabinets, wet drilling, or wet sawing of silica-containing materials to control the hazard and protect adjacent workers from exposure.
    4.    Routinely maintain dust control systems to keep them in good working order.
    5.    Practice good personal hygiene to avoid unnecessary exposure to other worksite contaminants such as lead.
    6.    Wear disposable or washable protective clothes at the worksite.
    7.    Shower (if possible) and change into clean clothes before leaving the worksite to prevent contamination of cars, homes, and other work areas.
    8.    Conduct air monitoring to measure worker exposures and ensure that controls are providing adequate protection for workers.
    9.    Use adequate respiratory protection when source controls cannot keep silica exposures below the designated limit.
    10.    Provide periodic medical examinations for all workers who may be exposed to respirable crystalline silica.
    11.    Post warning signs to mark the boundaries of work areas contaminated with respirable crystalline silica.
    12    Provide workers with training that includes information about health effects, work practices, and protective equipment for respirable crystalline silica.
    13.    Report all cases of silicosis to Federal / State health departments.
    8.0. Preventing damaging effects of air and dust pollution – The prevention of air pollution is world wide concern. There have been many investigations into what causes air pollution and the exact methods that work best in the prevention of air pollution. Through the use of many different methods air pollution is becoming easier to control. It is only through various measures, though, that the prevention of air pollution is possible. The government plays a very important role in prevention of air pollution. It is through government regulations that industries are forced to reduce their air pollution and new developments in technology are created to help everyone do their part in the prevention of air pollution. The government also helps by continuously making regulations stricter and enforcing new regulations that help to combat any new found source of air pollution.
    In many countries in the world, steps are being taken to stop the damage to our environment from air pollution. Scientific groups study the damaging effects on plant, animal and human life. Legislative bodies write laws to control emissions. Educators in schools and universities teach students, beginning at very young ages, about the effects of air pollution. The first step to solving air pollution is assessment. Researchers have investigated outdoor air pollution and have developed standards for measuring the type and amount of some serious air pollutants.
    Scientists must then determine how much exposure to pollutants is harmful. Once exposure levels have been set, steps can be undertaken to reduce exposure to air pollution. These can be accomplished by regulation of man-made pollution through legislation. Many countries have set controls on pollution emissions for transportation vehicles and industry. This is usually done to through a variety of coordinating agencies which monitor the air and the environment.
    In the prevention of air pollution it is important to understand about indoor air pollution. Indoor air pollution may seem like an individual concern, but it actually is not just something to worry about in your own home. Indoor air pollution contributes to outdoor air pollution. Prevention is another key to controlling air pollution. The regulatory agencies mentioned above play an essential role in reducing and preventing air pollution in the environment. In addition, it is possible to prevent many types of air pollution that are not regulated through personal, careful attention to our interactions with the environment. One of the most dangerous indoor air pollutants is cigarette smoke. Restricting smoking is an important key to a healthier environment. Legislation to control smoking is in effect in some locations, but personal exposure should be monitored and limited wherever possible.
    9.0. Conclusion – Air pollution prevention efforts of companies have generally focused on both source and waste reduction, and on reuse and recycling. Preventing air pollution within a company’s manufacturing processes remains the key approach. Cleaning and processing, switch to non-polluting technologies and materials, reduced generation of waste water, converting hazardous by-products to non-threatening forms, etc. have been attempted in this regard. Indirect air pollution prevention measures by companies also cover transportation. Examples of such measures include: providing company transportation to employees; offering commuting information and selling public transit passes; and encouraging employees to carpool and use public transportation. Companies have also initiated successful programmes such as the use of bicycles to commute to work, telecomuting, and work-at-home etc. to reduce pollution due to commuting.
    It should be noted that, only through the efforts of scientists, business leaders, legislators, and individuals can we reduce the amount of air pollution on the planet. This challenge must be met by all of us in order to assure that a healthy environment exist for ourselves and our children.
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    Did pilot commit SUICIDE? CIA boss says it is one theory agency is looking at as Malaysian police say they are carrying out psychological profiles of everyone on plane

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    Did pilot commit SUICIDE? CIA boss says it is one theory agency is looking at as Malaysian police say they are carrying out psychological profiles of everyone on plane


    This photo provided by Laurent Errera taken Dec. 26, 2011, shows the Malaysia Airlines Boeing 777-200ER that disappeared from air traffic control screens Saturday, taking off from Roissy-Charles de Gaulle Airport in France

    • CIA head John Brennan: 'No theory can be discounted' in hunt for clues
    • It came after he was asked if it was possible the pilot deliberately crashed
    • Brennan also said 'terrorism has not yet been ruled out of investigation'
    • Malaysian police say one of the two men on stolen passports was Iranian
    • Was asylum seeker, 19, 'not terrorist', and his mother was waiting for him
    • Smartphones of missing aboard flight MH370 'are still ringing', families say
    • 19 families of missing claim to be connected - airline have also called crew
    • Growing frustration for relatives with no information on their missing
    • Angry relatives threw water bottles at officials unable to offer any answers
    Authorities are investigating the possibility that the pilot of the missing Malaysian Airlines flight MH 370 committed suicide, the director of the CIA has revealed. 
    John Brennan, head of the US Central Intelligence Agency (CIA), said: 'I think you cannot discount any theory', when asked if it was possible the pilot deliberately crashed the Boeing 777.
    His intervention came as Malaysian police say they are carrying out psychological profiles of everyone on board the plane, which vanished on Saturday carrying 239 people after taking off from Kuala Lumpur en route to Beijing.
    The theory could offer an explanation as to how the plane 'disappeared' from civilian radar tracking its movements, as the pilot could simply have switched off the transponder shortly before it vanished.
    Scroll down for video

    Authorities are investigating the possibility that the pilot of the missing Malaysian Airlines flight MH 370 committed suicide, John Brennan the director of the CIA has revealed
    Authorities are investigating the possibility that the pilot of the missing Malaysian Airlines flight MH 370 committed suicide, John Brennan the director of the CIA has revealed
    Head of the US Central Intelligence Agency (CIA), said: 'I think you cannot discount any theory', when asked if it was possible the pilot deliberately crashed the Boeing 777
    Head of the US Central Intelligence Agency (CIA), said: 'I think you cannot discount any theory', when asked if it was possible the pilot deliberately crashed the Boeing 777
    Jonti Roos (centre) claims she and her friend were entertained by Fariq Abdul Hamid, 27, who is one of the pilots of the missing Malaysia Airlines flight (right)
    Jonti Roos (centre) claims she and her friend were entertained by Fariq Abdul Hamid, 27, who is one of the pilots of the missing Malaysia Airlines flight (right)
    The two men who travelled on the doomed Malaysian Airlines flight from Kuala Lumpur to Beijing on stolen passports. The younger man (left) was identified as Pouiria Nur Mohammad Mehrdad, 19, said by police in Malaysia to be an Iranian asylum seeker on his way to Germany to meet his mother. The older man (right) remains unknown.
    The two men who travelled on the doomed Malaysian Airlines flight from Kuala Lumpur to Beijing on stolen passports. The younger man (left) was identified as Pouiria Nur Mohammad Mehrdad, 19, said by police in Malaysia to be an Iranian asylum seeker on his way to Germany to meet his mother. The older man (right) remains unknown.
    Media interest: Relatives of Chinese passengers on Malaysia Airlines flight MH370 were still clutching to faint straws of hope for their loved ones on March 11, four days after the aircraft went missing
    Media interest: Relatives of Chinese passengers on Malaysia Airlines flight MH370 were still clutching to faint straws of hope for their loved ones on March 11, four days after the aircraft went missing
    Agonizing wait: Chinese relatives of passengers aboard a missing Malaysia Airlines plane wait for the latest news inside a hotel room for relatives or friends of passengers aboard the missing airplane in Beijing, China Tuesday, on March 11, 2014.
    Agonizing wait: Chinese relatives of passengers aboard a missing Malaysia Airlines plane wait for the latest news inside a hotel room for relatives or friends of passengers aboard the missing airplane in Beijing, China Tuesday, on March 11, 2014.
    Emotional: A relative of passengers on Malaysia Airlines flight MH370 cries in the waiting lounge in Lido Hotel in Beijing
    Emotional: A relative of passengers on Malaysia Airlines flight MH370 cries in the waiting lounge in Lido Hotel in Beijing

    Interpol chief statement as passport imposter is exposed
    Brennan also said that terrorism could not be ruled out in the disappearance of the airliner.
    'Could it just have been some kind of catastrophic event? I do not think people at this point should rule out any lines of inquiry.'
    'I think there's a lot of speculation right now - some claims of responsibility that have not been, you know, confirmed or corroborated at all,' he said.
    He added that there were a host of unanswered questions including why the plane's transponder stopped emitting signals and what was the role of passengers carrying stolen passports.

    WHAT COULD HAVE HAPPENED?

    A mid-air explosion: The lack of debris could be explained by it falling into Malaysian jungle
    A terrorist attack: Director of CIA has said terrorism could not be ruled out
    Power failure: Possibly caused by deliberate cutting of power to communication instruments
    Electronic warfare: 20 passengers on board were experts in this technology.
    Hijacking: Radar data indicates the plane might have made a U-turn.
    A pilot error: There is a chance of them in all air mysteries, claim experts
    Structural failure: Possibly involving damage sustained by an accident in 2012
    Pilot suicide: There were two large jet crashes in the late 1990s caused by this
    Aeronautical black hole: Plane is stranded hundreds of miles from current search area
    'There are a number of very curious anomalies about all of this...You know, did it turn around? You know, were the individuals with these stolen passports in any way involved?'
    He added: 'What about the transponder? Why did it sort of, you know, just disappear from the radar?'
    The former counter-terrorism adviser to President Barack Obama said there had been 'some claims of responsibility' over the missing jet that had 'not been confirmed or corroborated'.
    But when asked if he could rule out a terrorist link, Brennan said: 'No, I wouldn’t rule it out.'
    He said there were many unanswered questions about the Malaysia Airlines flight.
    He said: 'We are looking at it very carefully. Clearly this is still a mystery.'
    He added: 'I think at this point we again have to be patient and wait for the authorities to investigate.
    'There are many questions. Who had the ability to turn off the transponder? How can one such action be masked?
    Brennan's comments came at a rare public speaking appearance at an event in Washington organised by the Council on Foreign Relations, a think tank.
    Earlier today relatives claimed they were able to call the cellphones of their missing loved ones
    According to the Washington Post, family of some of the 239 people on board the vanished Boeing 777 said that they were getting ring tones and could see them active online through a Chinese social networking service called QQ.
    One man said that the QQ account of his brother-in-law showed him as online, but frustratingly for those waiting desperately for any news, messages sent have gone unanswered and the calls have not been picked up.
    This new eerie development comes as the Malaysian authorities said they had identified one of the men on two stolen European passports who were on the flight - and that he was not considered likely to be a terrorist. 
    CIA: Can't rule out terrorism in Malaysia plane mystery
    Separately, the search for any trace of the missing airliner has now shifted to the Straits of Malacca, at least 100 miles away from where it was last recorded by electronic monitoring devices.
    The dramatic shift raises the possibility that it flew undetected, crossing mainland Malaysia, before ditching into the sea.
    However the phantom phone calls and online presence set off a whole new level of hysteria for relatives who have spent the past three-days cooped-up in a Beijing hotel waiting for some concrete information on the missing plane.
    Repeatedly telling Malaysian Airlines officials about the QQ accounts and ringing telephone calls, they hoped that modern technology could simply triangulate the GPS signal of the phones and locate their relatives. 
    However, according to Singapore's Strait Times, a Malaysia Airlines official, Hugh Dunleavy has confirmed to families that his company had tried to call the cellphones of crew members and they too had also rang out.
    He is reported to have told relatives that those phone numbers have been turned over to Chinese authorities.
    One man who had asked police to come to his house and see the active QQ account on his computer was devastated to see that by Monday afternoon it had switched to inactive.
    According to China.org.cn, 19 families of those missing have signed a joint statement confirming that their calls connected to their loved ones but that they rang out.
    The relatives have asked for a full investigation and some complained that Malaysian Airlines is not telling the whole truth.
     
    MH370: Families in tears as they continue to wait for news

    Family members of passengers onboard flight MH370 arrive in a car to the hotel they are staying at, in Putrajaya on March 11, 2014
    Family members of passengers onboard flight MH370 arrive in a car to the hotel they are staying at, in Putrajaya on March 11, 2014
    Family members of passengers onboard the missing Malaysia Airlines flight MH370 from Beijing arrive at Cyberview Lodge Hotel as they await news on their missing loved ones
    Family members of passengers onboard the missing Malaysia Airlines flight MH370 from Beijing arrive at Cyberview Lodge Hotel as they await news on their missing loved ones
    No answers yet: Family members from Beijing, China, of a missing Malaysian Airlines flight arrive at a hotel in Cyberjaya, near Kuala Lumpur International Airport, Sepang, Selangor, Malaysia on Tuesday morning
    No answers yet: Family members from Beijing, China, of a missing Malaysian Airlines flight arrive at a hotel in Cyberjaya, near Kuala Lumpur International Airport, Sepang, Selangor, Malaysia on Tuesday morning
    Hopeful family members from Beijing, China, of a missing Malaysian Airlines flight arrive at a hotel in Kuala Lumpur International Airport on Tuesday morning as they wait for any news
    Hopeful family members from Beijing, China, of a missing Malaysian Airlines flight arrive at a hotel in Kuala Lumpur International Airport on Tuesday morning as they wait for any news
    A board displaying messages for the passengers from the missing Malaysia Airlines flight MH370 is seen at Kuala Lumpur International Airport in Sepang on March 11, 2014
    A board displaying messages for the passengers from the missing Malaysia Airlines flight MH370 is seen at Kuala Lumpur International Airport in Sepang on March 11, 2014
    The International Business Times reported that the sister of one of the Chinese passengers also rang his phone on live television.
    'This morning, around 11:40, I called my older brother's number twice, and I got the ringing tone,' said Bian Liangwei, sister of one of the passengers according to IBT.
    At 2pm, Bian called again and heard it ringing once more.
    'If I could get through, the police could locate the position, and there's a chance he could still be alive.'
    However, at a press conference in Beijing, Malaysian Airlines spokesman Ignatius Ong said one of the numbers that had been passed on to the airline's head office in Kuala Lumpur failed to get through.
    'I myself have called the number five times while the airline's command center also called the number. We got no answering tone,' said Ong.
    Indeed, authorities Authorities hunting for the missing Malaysia Airlines jetliner expanded their search on land and sea Tuesday, reflecting the difficulties in locating traces of the plane more than three days after it vanished.
    Malaysia Airlines said in a statement the western coast of the country, near the Straits of Malacca, was 'now the focus' of the hunt. That is on the other side of peninsular Malaysia from where flight 370 was reported missing.

    WHY ARE THE PASSENGERS' PHONES STILL RINGING?

    After three days, wouldn’t the phone batteries be dead by now?
    Not necessarily. Smartphones are renowned for their poor battery life and will typically last up to around 24 hours. But the batteries of older phones can last considerably longer.
    For example, the Nokia 100 boasts a standby battery life of a staggering 35 days. Smartphone batteries can also last longer if the handset isn’t being used, and especially if the phone is in Flight Mode.
    However, if the phone is in Flight Mode, it switches off all wireless activity meaning calls wouldn’t be able to connect, effectively ruling out this theory.  If the phone batteries are dead, wouldn’t the call go straight to voicemail?
    In a word, yes. However, the process of sending the call to voicemail can differ depending on the service provider.
    For example, the majority of phones will go straight to voicemail, or callers will get an out of service message if voicemail hasn’t been set up.
    This will occur even if the phone is underwater, or not near a cell signal.
    However, some service providers will ring once or twice before the phone goes to voicemail, or cut off. This may explain the reports that claimed phones rang before seeming to hang up. Some reports claim the phones are just ringing and ringing though. How is this possible?
    Telecoms expert Alan Spencer told MailOnline that if the phones are really ringing, they can categorically not be under the sea.
    He added that the phones will only be ringing if they are ‘switched on, not in water, the battery is charged, and [they are] near a mobile cell site.’
    This means that if the phones are genuinely ringing, the plane needs to have landed on land – not in the sea – and be in a location where there is cell service, rather than landing in the middle of a jungle, for example. Why can’t network operators locate the phones?
    A number of family members have asked the network operators why they can’t use the phone’s signal to locate the missing people.
    Professor William Webb, a Fellow of the Royal Academy of Engineering, told MailOnline: ‘The phones definitely won't be working. They'll be underwater, out of coverage and by this time out of battery.
    ‘So there's absolutely no way they could be used for triangulation.
    ‘As to why they are ‘ringing’ it'll be the same as if they were out of coverage - in some cases it may ring before going to voicemail.’What about the T3212 timer I’ve read about?
    The T3212 is a timer that causes a phone to periodically send a message to the network saying where it is.
    But Professor Webb said this only works when the phone is turned on and it is in coverage. It won't work when the battery is dead.
    What about reports that passengers are appearing online, on the QQ social network?
    When people sign into social networks including QQ, as well as Facebook, they appear online.
    This is the case whether they’ve signed in on a phone, tablet, PC, and laptop.
    if missing passengers are shown as online, they may not be using the service on their phone. Instead they may still be logged in on another device.
    If this other device shuts down or goes into standby, however, or there is a long period of inactivity, the social network will log them out, which may explain why some accounts went from online to offline over a period of three days.
    Shift of focus: Azharuddin Abdul Rahman (R), director general of the Department of Civil Aviation of Malaysia, speaks during a press conference on March 10, 2014 in Kuala Lumpur, Malaysia
    Shift of focus: Azharuddin Abdul Rahman (R), director general of the Department of Civil Aviation of Malaysia, speaks during a press conference on March 10, 2014 in Kuala Lumpur, Malaysia
    Vietnamese officers discuss their plan during a meeting before a mission to find the missing Malaysia Airlines flight MH370 at Phu Quoc Airport on Phu Quoc Island March 11, 2014
    Vietnamese officers discuss their plan during a meeting before a mission to find the missing Malaysia Airlines flight MH370 at Phu Quoc Airport on Phu Quoc Island March 11, 2014
    Civil aviation chief Azharuddin Abdul Rahman said the statement didn't imply authorities believed the plane was off the western coast. 'The search is on both sides,' he said.
    The Boeing 777 had 239 people on board when it vanished off radar screens early Saturday morning en route to Beijing from Kuala Lumpur, triggering a massive international search effort.
    Authorities began their hunt at the point the plane was last known to be, a spot in the seas between Malaysia and Vietnam. With no debris found, they have systematically expanded their search to include areas where the plane could have in theory ended up given the amount of fuel it had on board.
    They have also said that the plane might have tried to turn back to Kuala Lumpur. On Sunday, Malaysia's air force chief said there were indications on military radar that the jet may have done a U-turn.
    Vietnamese planes and ships are a major component of the international search and rescue effort.

    Search: A U.S. Navy SH-60R Seahawk helicopter takes off from the destroyer USS Pinckney in the Gulf of Thailand, to assist in the search for missing Malaysian Airlines flight MH370 on Monday
    Search: A U.S. Navy SH-60R Seahawk helicopter takes off from the destroyer USS Pinckney in the Gulf of Thailand, to assist in the search for missing Malaysian Airlines flight MH370 on Monday
    Lt. Gen. Vo Van Tuan, deputy chief of staff of Vietnamese People's Army, said authorities on land had also been ordered to search for the plane, which could have crashed into mountains or uninhabited jungle.
    He said that military units near the border with Laos and Cambodia had been instructed to search their regions also.
    'So far we have found no signs (of the plane) ... so we must widen our search on land,' he said.
    Experts say possible causes of the apparent crash include an explosion, catastrophic engine failure, extreme turbulence, pilot error or even suicide.
    This deepening of the already baffling mystery into the disappearance of flight MH370 comes as it was claimed that the two passengers traveling on stolen passports on the plane were Iranian nationals.
    A friend of one of the two men told BBC Persia that he played host to the pair in Kuala Lumpur after their arrival from Tehran before they took off on the fateful journey.

    This photo provided by Laurent Errera taken Dec. 26, 2011, shows the Malaysia Airlines Boeing 777-200ER that disappeared from air traffic control screens Saturday, taking off from Roissy-Charles de Gaulle Airport in France
    This photo provided by Laurent Errera taken Dec. 26, 2011, shows the Malaysia Airlines Boeing 777-200ER that disappeared from air traffic control screens Saturday, taking off from Roissy-Charles de Gaulle Airport in France
    The source told the BBC service that the pair had bought the fake passports because they wanted to go and live in Europe.
    The two men were using the passports of Christian Kozel - a 30-year-old Austrian and Luigi Maraldi, a 37-year-old Italian.
    The friend, who knew one of the men from school said that both purchased the illegal and fake passports in Malaysia and one-way tickets to Amsterdam.
    BBC Persia's UN correspondent Bahman Kalbasi told the UK's Daily Telegraph newspaper that the two men were not sinister and were only 'looking for a place to settle.'
    Investigators in Malaysia are voicing skepticism that the airliner that disappeared early Saturday with 239 people on board was the target of an attack, U.S. and European government sources close to the probe said.

    How the search is widening - but has still to find a thing: Strait of Malacca is now main focus of air and sea search but China is deploying ships, planes and helicopters to the South China Sea to try to find any trace of the Boeing 777. Its authorities say more needs to be done to find what happened to the plane.
    How the search is widening - but has still to find a thing: Strait of Malacca is now main focus of air and sea search but China is deploying ships, planes and helicopters to the South China Sea to try to find any trace of the Boeing 777. Its authorities say more needs to be done to find what happened to the plane.
    The fate of the Malaysian airliner that vanished about an hour into a flight to Beijing remained a mystery, as a massive air and sea search, now in its fourth day, failed to turn up any trace of the Boeing 777 plane.
    Neither Malaysia's Special Branch, the agency leading the investigation locally, nor spy agencies in the United States and Europe have ruled out the possibility that militants may have been involved in downing Malaysia Airlines Flight.
    But Malaysian authorities have indicated that the evidence so far does not strongly back an attack as a cause for the aircraft's disappearance, and that mechanical or pilot problems could have led to the apparent crash, the U.S. sources said.
    'There is no evidence to suggest an act of terror,' said a European security source, who added that there was also 'no explanation what's happened to it or where it is.'

    Chinese and international journalists wait at the check-in area for Malaysian Airlines at Capital Airport in Beijing, China on Monday
    Chinese and international journalists wait at the check-in area for Malaysian Airlines at Capital Airport in Beijing, China on Monday
    Meanwhile, dozens of ships and aircraft from 10 countries were still scouring the seas around Malaysia and south of Vietnam as questions mounted over possible security lapses that could have led to a downing of the Boeing 777-200ER after it climbed to an altitude of 35,000 feet.
    Interpol confirmed on Sunday at least two passengers used stolen passports and said it was checking whether others aboard had used false identity documents.
    Even so, one U.S. source said Malaysian authorities were leaning away from the theory that the plane was attacked.
    Their view was mostly based on electronic evidence that indicates the flight may have turned back toward the Malaysian capital of Kuala Lumpur before disappearing.
    Even that information has not been clearly confirmed, and investigators and intelligence sources say the fate of the Flight MH370 is still shrouded in mystery.

    Chinese students stand by candles while praying for the passengers aboard the missing Boeing 777-200 plane of Malaysia Airlines Flight MH370 at a school in Zhuji city, east Chinas Zhejiang province
    Chinese students stand by candles while praying for the passengers aboard the missing Boeing 777-200 plane of Malaysia Airlines Flight MH370 at a school in Zhuji city, east Chinas Zhejiang province
    One reason was that the aircraft had failed to make automatic contact with a flight data-monitoring system after vanishing from radar screens, two people familiar with the matter said on Monday.
    Such contact could have helped investigators determine what happened.
    Also raising doubts about the possibility of an attack, the United States extensively reviewed imagery taken by spy satellites for evidence of a mid-air explosion, but saw none, a US government source said. The source described U.S. satellite coverage of the region as thorough.
    With no success so far, authorities were planning to widen the search from Tuesday, Azharuddin Abdul Rahman, the head of Malaysia's Civil Aviation Authority, told reporters on Monday.
    'Unfortunately we have not found anything that appears to be objects from the aircraft, let alone the aircraft,' he said.
    'As far as we are concerned, we have to find the aircraft. We have to find a piece of the aircraft if possible.'
    Azharuddin said a hijacking attempt could not be ruled out as investigators explore all theories.

    Frustrated relatives of Chinese passengers threw water bottles at airline officials during briefing

    Angry relatives threw water bottles at Malaysia Airlines officials after they were unable to offer any more information on the disappearance of flight MH370.
    Four members of staff of the airline faced relatives of Chinese passengers on board the flight during a briefing yesterday afternoon.
    According to The New York Times, one of the relatives shouted 'All Malaysians are liars', before adding 'do you know what "liars" means?'

    Hugh Dunleavy (second right) and Ignatius Ong (second left) from Malaysia Airline attend a conference with Chinese relatives of the passengers onboard flight MH370 at the Lido Hotel
    Hugh Dunleavy (second right) and Ignatius Ong (second left) from Malaysia Airline attend a conference with Chinese relatives of the passengers onboard flight MH370 at the Lido Hotel
    Nearly 100 people crammed themselves into the room for the 20-minute briefing, which journalists were officially barred from, the paper reported.
    Meanwhile, more than 100 of the relatives, who have been holed up in a Beijing hotel anxiously awaiting news of their family members, have signed a petition demanding answers and government assistance, The Washington Post has reported.
    The airline sent professionals to counsel and support the families over the weekend.
    Over the last three days the search mission has grown to include nine aircraft and 24 ships from nine countries, which have been scouring the Gulf of Thailand on the eastern side of Malaysia.
    Apart from the sea, land areas are also being searched.

    Chinese relatives of the passengers onboard Malaysia Airlines flight MH370 gather inside the waiting area at Lido Hotel
    Chinese relatives of the passengers onboard Malaysia Airlines flight MH370 gather inside the waiting area at Lido Hotel
    A relative (centre) of passengers on the missing Malaysia Airlines flight MH370 speaking to journalists in the Lido Hotel in Beijing
    A relative (centre) of passengers on the missing Malaysia Airlines flight MH370 speaking to journalists in the Lido Hotel in Beijing
    China, where two-thirds of the passengers were from, has urged Malaysian authorities to 'speed up the efforts' while also contributing ships and helicopters to the search.
    The plane took off from Kuala Lumpur, on the western coast of Malaysia, early Saturday en route to Beijing. It flew overland across Malaysia and crossed the eastern coast into the Gulf of Thailand at 35,000 feet (11,000 meters).
    There it disappeared from radar screens. The airline says the pilots did not send any distress signals, suggesting a sudden and possibly catastrophic incident.

    A relative of a Chinese passenger onboard Malaysia Airlines flight MH370 answers questions from the media at the Lido Hotel
    A relative of a Chinese passenger onboard Malaysia Airlines flight MH370 answers questions from the media at the Lido Hotel
    In a statement, Malaysia Airlines said search and rescue teams 'have expanded the scope beyond the flight path to the West Peninsula of Malaysia at the Straits of Malacca'.
    An earlier statement had said the western coast of Malaysia was 'now the focus', but the airline subsequently said that phrase was an oversight.
    'The search is on both sides,' Civil aviation chief Azharuddin Abdul Rahman said, adding that the previous statement didn't mean that the plane was more likely to be off the western coast.

    How India's upcoming green regulator can strike a balance between growth & environmental protection

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    How India's upcoming green regulator can strike a balance between growth & environmental protection

    M Rajshekhar, ET BureauMar 11, 2014, 03.34AM IST
     (The regulator should have…)
     India's environmental clearance process is universally loathed. Industry and technocrats find it cumbersome and corrupt, and blame it for project delays and slowing growth. Environmentalists and project-affected people consider it superficial, corrupt and given to approving virtually all projects, unmindful of their social and environmental costs.
    Both views are correct. India's environmental clearance (EC) process is a mess, unable to strike a balance between the demands of growth and the need to protect the ecological systems needed to support what will soon be the world's most populous country.
    William Lockhart , the emeritus professor of law at University of Utah's SJ Quinney College of Law, has been studying India's EC process for a long time, and he pans every part of it. "Clearances of all sorts are approved with minimal or no meaningful environmental review, under constant political pressure, on the basis of 'future' compliance with 'conditions' for post-clearance performance on matters that are required by law to be assessed before clearance, and in any event remain almost wholly unenforced." That is the bad news.
    The good news is this could change. On January 6, the country's highest court, assessing the ministry of environment's mechanism t o appraise projects to be "not satisfactory", directed it to set up by March 31 an independent regulator that would appraise, approve and monitor projects.
    A set of bureaucrats in the ministry is currently working on the architecture of the new regulator. But will this new architecture address the shortcomings that plague each of the four steps of the EC process?
    Step 1: Impact Study
    The first step is assessing the environmental impact of a project. At present, private consultants or Indian academic institutions (like IIT Roorkee) conduct environmental impact assessment (EIA) studies. But since they are funded by project proponents, EIAs inevitably under-report environmental costs. Some years ago, after persistent complaints about poor EIA studies, the ministry asked the Quality Council of India to accredit EIA agencies. A ministry official working on the new regulator says this has not worked. "None of the companies being empanelled as EIA consultants understands ecosystem services—everything that an environment provides," says this official, on the condition of anonymity.
    The ministry, this official adds, is weighing two changes. First, it is considering a system where the regulator accredits EIA agencies on its own; at the very least, participates in the process. Second, it wants to create a new body, containing environmental information from satellites, Forest Survey of India, etc, which can be used to authenticate claims in EIA reports—for example, about the distance between a project site and the nearest forest or river.

    Step 2: Expert Verdict
    Once an EIA report is prepared, it goes to an expert appraisal committee (EAC), be it at the Centre or at the state level. EACs comprise experts from various fields who meet, usually monthly, to assess the EIA reports and recommend clearance (or not) to the ministry.
    Most EAC members belong to the very industry whose projects they vet. Some of the outcomes give cause for concern. For example, a February 2013 study by the South Asia Network on Dams, Rivers and People, a Delhibased anti-dam organisation, noted the hydel EAC, in its six years, had evaluated 262 hydropower and irrigation projects. It did not reject even one.
    There is also conflict of interest. Former power secretary Paul Abraham was the chairman of the hydel EAC between 2007 and 2009. During this period, he was also on the board of hydel companies and companies that had invested in them. Abraham says he would recuse himself when the projects of these companies came up.
    However, the minutes of the 11th meeting of the EAC on February 20-21, 2008 show he chaired the meetings where two projects of Athena Demwe were taken up and approved. Abraham was on the board of PTC, which was an equity investor in Athena Demwe.
    Another factor is lack of support. Last year, a senior member of the hydel EAC, who has since stepped down, told ET that norm-setting was a problem. "There are no internal regulations on norms for hydel —be it the minimum flow or the gap between projects. None of this has been defined," he said. "The EAC has just worked out some norms on its own." The SC judgement refers to this, observing that "lack of permanence in the expert appraisal committees leads to lack of continuity and institutional memory, leading to poor knowledge management".

    India grows, environment pays the cost

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    India grows, environment pays the cost

    Chetan Chauhan, Hindustan Times New Delhi, March 01, 2014
    First Published: 21:43 IST(1/3/2014) | Last Updated: 11:52 IST(2/3/2014)
    India has driven the truck of development — loaded with tar, bricks, glass, concrete…the works — right through its most treasured and fragile green spaces in the last decade. While major cities like Delhi and Mumbai sacrificed green cover for real estate, the country's finest wildlife corridors have been ceded to indiscriminate industrialisation.
    In the absence of a clear policy to balance development and environment, the Aravallis in Gurgaon, Western Ghats spread across five states, biodiversity of the Northeast and the forests in tribal districts (one-fifth of the country’s 640 districts) have taken a hit.
    India lost 135 hectares of forest — think 190 full-sized football fields — daily to industrial projects in 2013 compared with about 80 hectare two decades ago, showed an RTI reply by the environment ministry.
    Nothing will change unless environement protection is made independent of the government, say environmentalists (HT photo)

    The government records, however, fail to depict the true degradation, thanks to Forest Survey of India (FSI) showing rubber plantations and apple orchards as green cover. “The trick is that the forest department manages to add compensatory afforestation programmes to the total green cover,” said Neeraj Vagholikar of environmental group Kalpavriksh.
    Western Ghats’ forests — spread across Gujarat, Maharashtra, Karnataka, Andhra Pradesh and Kerala — shrunk by about 25% in two decades because of reckless mining and quarrying.
    Stalin D of environmental group Vanashakti said the government had meekly surrendered to the “development lobby which sought a free hand to unleash destruction”. Madhav Gadgil, who headed an ecological expert panel on the Western Ghats, said if restrictions were not imposed, we would lose pristine ecology to “those who send bags of money to politicians”.
    In spite of a 2005 Bombay high court order declaring mangroves as forests, rampant reclamation of mangrove-rich coasts is making way for housing projects and industries in Maharashtra.
    In the Northeast, a probe panel set up by the Supreme Court in 2011 found that 39% land at nine cement plants in Meghalaya were forests. Around 10,000 hectares of forest has been encroached by tea estates in Assam.
    About 80 hydel projects in Arunachal Pradesh approved in the last three years would wipe out hundreds of acres of forest including the habitat of the Black Neck Crane, considered the embodiment of the sixth Dalai Lama, and the Bengal Florican, a critically endangered species.
    Northeast’s jewel, the Kaziranga National Park, home to tigers and the single-horn rhino, has been damaged by stone quarries, stone crushes, brick kilns and other industrial units within the notified ‘no development zone’.
    “The environment ministry and the Assam government allowed the mushrooming of industrial units including private tea factories in this sensitive zone,” said Rohit Choudhury, an activist who lives near Kaziranga.
    Elsewhere, it is the same story.
    Odisha, Jharkhand, Chhattisgarh and Goa have all lost green cover to aggressive mining. The MB Shah Commission, which investigated illegal mining in these states, accused the environment ministry of allowing plunder at the cost of the exchequer.
    In Odisha alone, the panel said, illegal mining worth Rs. 59,000 crore was allowed. Around 16,000 hectare of forest — half of it in Keonjhar district — was lost to mining. Odisha principal chief conservator of forest JD Sharma, however, said there was no violation.
    “When we find any discrepancy, we initiate action,” he said.
    Among more than 100 projects cleared, environment minister Veerappa Moily this February allowed mining in the core area of an elephant reserve in Jharkhand. Earlier, the ministry approved mining in the green corridor used by elephants and tigers to move from one reserve to another in Maharashtra and Chhattisgarh.
    Forest loss because of rampant mining had prompted Tribal Affairs minister V Kishore Chandra Deo to seek a ban on mining in tribal areas including in his home state Andhra Pradesh, where about 1,500 hectares in Visakhapatnam cleared for bauxite mining is under litigation.
    “Mining clearances are being given without a thorough environmental and social impact assessment. This leads to rapid forest degradation and unrest among local tribals dependent on these forests for their livelihood,” said Srinivas Ganjivarapu, environmental activist based in Visakhapatnam.
    Closer home in Delhi, green regulations are getting compromised within 40 km of the ministry’s headquarters at Paryavaran Bhawan.
    The National Capital Region Planning Board plans to allow 0.5% of Aravallis for construction and tourism on the ground of land constraint, by leasing the capital’s green lungs to colonisers. The state had sought permission from courts to set up a Disneyland, a technology park and a film city. The courts refused permission.
    In UP, sand mining and unauthorised construction on Yamuna banks goes on unabated, resulting in shrinking of wetlands from 19 in 2009 to 6 in 2011. “Ironic that a state, which is willing to spend Rs. 2,000 crore on an artificial night zoo, is not protecting its natural gifts,” said Vikrant Tongad, a local environmentalist.An officer like Durga Shakti Nagpal, who challenged the mining mafia, was suspended in 2013 for stopping illegal sand mining in Gautam Budh Nagar. A young IPS officer, Narendra Kumar Singh, was crushed under a tractor in MP’s Morena in 2012 when he tried stopping illegal sand mining.
    “Nothing much will change unless environment protection is made independent of the government. There needs to be transparency in clearing projects and strict penalties for violation,” said Sunita Narian, director general of Delhi-based advocacy group Centre for Science and Environment.
    (With inputs from Prasad Nichenametla, Rahul Karmakar, Priyaranjan Sahu, Vinod Rajput and Snehil Sinha)

    PLEASE MAKE KAKINADA AS CAPITAL, Kakinada will be the best capital of Seemandhra

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    Kakinada will be the best capital of Seemandhra , here all type of infrastructure can be developed with latest ideas & technology , all industrialist will support for it 

    History of Kakinada

    Kakinada is a city and a municipal corporation in the Indian state of Andhra Pradesh. It is located 465 kilometres (289 mi) east of the state capital, Hyderabad. It is also the headquarters of East Godavari district. It is nicknamed 'Fertilizer City' (owing to the large concentration of fertiliser plants), 'Pensioner's Paradise' and 'Second Madras'. The city had an urban population of 312,255 in 2011, making it the fourth largest city by area and the sixth largest city by population in Andhra Pradesh. Its urban/metropolitan population is 442,936 of which 217,573 are males and 225,363 are females. The sex ratio of Kakinada city is 1046 per 1000 males. It is spread over an area of 90 km. Kakinada is part of a Special Economic Zone and a proposed 'Petroleum, Chemical and Petrochemical Investment Region (PCPIR)'. It is a hub to all the deep sea exploratory activity in the region due to its deep-water sea port and its proximity to the gas fields.

    Etymology

    Several theories exist regarding the origin of the name Kakinada. One is that the place was called 'Kakinandiwada' during the reign of Nandi kings who ruled prior to the arrival of the Europeans and the name was truncated to Kakinada over time. The British used to call it Cocanada (pronounced 'Caa-key-naada'). After Independence, the name was renaturalised to Kakinada, although a few organisations established during the British colonial rule retain the old name (e.g., Cocanada Chamber of Commerce). As per history this place was full of ponds filled with red lotus which is called as Kokanadamu in Telugu. Eventually this became CoCanada during the British rule. Even now, the City's two railway stations are codenamed CCT (Kakinada Town Junction) and COA (Kakinada Port) by Indian Railways. Kakinada is also known as 'Pensioners Paradise', as it shares it calm and pleasant environment to the retired and old-age people. Some of the people locally conjures Kakinada as second MADRAS as they have some similar properties.

    Geography

    Kakinada is located at 16.93°N 82.22°E. The 82½ degrees east longitude, with respect to which IST (Indian Standard Time) is calculated, passes through Kakinada. It has an average elevation of 2 metres (6 ft) and many areas of the city are below sea level. The city has roughly a north-south orientation and is confined to a long narrow strip parallel to the sea coast. The average width of the city is around 6 km but its length is around 15 km. It can be divided into two broad regions. The city in the south called Jagannathapuram is separated from the rest of the city by Buckingham Canal. A couple of bridges connect these parts. This canal and its branches form Medaline Island, which abuts the city in the southwest. The northern part consists of the more modern part of the city and its recent outgrowth. The eastern part is separated from coastline by an industrial belt, running north-south through the entire length of the city. The city is bordered in the south east by Kakinada bay and a marshy wetland, home to India's second largest mangrove forest and Coringa Wildlife Sanctuary. One of the branches of the mighty River Godavari, the Gouthami, flows into the Bay of Bengal at this point.

    Distances to other cities in Andhra Pradesh:

    Hyderabad: 500 km
    Vijayawada: 210 km
    Visakhapatnam: 160 km
    Rajahmundry: 60 km
    Tirupati: 600 km
    Warangal: 390 km

    Climate

    Kakinada has a tropical savanna climate. The weather is hot and humid for most of the year. The hottest part of the year is late May to early June with maximum temperatures around 38–42 °C (100–108 °F). The coolest part of the year is January, with minimum temperatures around 18–20 °C (64–68 °F). The city gets most of its seasonal rainfall from the south-west monsoon winds although a good deal of rains greet these parts during the northeast monsoon from mid-October to mid-December. Cyclones in the Bay of Bengal frequently hit the city. Prevailing winds in Kakinada are usually southwesterly for most part of the year except during October to January when they blow north-easterly. The city experiences an average annual rainfall between 110 and 115 centimetres.

    Civic Administration

    The city of Kakinada is run by the Kakinada Municipal Corporation, consisting of elected representatives and a commissioner. The city is divided into 50 wards and each ward elects a corporator through direct ballot. A mayor is elected for the entire city among the elected corporators by indirect ballot. The commissioner who is an IAS is appointed by the state government. Apart from this, the city is represented at the state level in the Andhra Pradesh State Legislative Assembly by two MLAs and at the federal level in the Lok Sabha by an MP.

    Transportation

    Air

    The nearest airport is located at Rajahmundry, about 65 km.Rajahmundry City Airport has services to Chennai, Hyderabad, Vijayawada and Bangalore. Kingfisher Airlines, Jet Airways and Spice Jet are the airlines operating here. The other nearest major airport is at Visakhapatnam at a distance of 145 km and has the services of many airline operators to major cities in the country.and there was aproposal to build an international airport equidistant from kakinada and vishakapatnam.

    Rail

    As a city located on the sea shore, Kakinada is a railway terminus. It has four railway stations, namely Kakinada Town Junction (1.2 km), Kakinada Port (1.8 km), Kakinada Port New (4.1 km), and Sarpavaram (6.5 km). Through a branch line, Kakinada is connected to Samalkot Junction (13 km) which is on the Chennai-Howrah trunk line, where almost all express trains stop to connect Kakinada with the important places of the country. There are direct daily trains running to Hyderabad, Mumbai, Bangalore, Chennai, Tirupati, Shirdi(tri weekly) and Bhavnagar (weekly) and also special trains running all through the year to Hyderabad and Ernakulam. There is a demand for construction of the long waited Kakinada – Pitapuram railway line of 21 km length which connects Kakinada to the main line apart from extending the Kakinada-Kotipalli railway line to Narsapur which will bring rail connectivity to Konaseema region.according to railway budjet few trains will be started to mumbai,a/c train to secunderabad and howrah from kakinada.

    Road

    Good roads connect Kakinada with all the places within the state and rest of the country. NH-214 from Kathipudi to Ongole (both on NH-5) passes through Kakinada. A couple of state highways connect Kakinada to Rajahmundry and other places within the district. There is a proposal to develop the road between Kakinada and Suryapet via Rajahmundry into a National Highway which will reduce the distance between Kakinada and Hyderabad.

    Economy

    In the late 1940s (around the time of Indian independence) there was little industry in or around Kakinada, and the local economy consisted mainly of agriculture and fishing. Until the early 1980s (before the fertiliser companies started their operation here), the local economy was mainly based on the textile industry, auto parts, steel industry related ancillary units, agriculture and fishery industries. Today, Kakinada's economy has a diverse industrial base thanks to an established sea port and port based industries.

    Kakinada Port

    The presence of a small island called Hope Island about 5 km from Kakinada coast makes Kakinada a natural harbour. It is home to two ports, an anchorage port and a deep water port. Kakinada's deep-water port is the second largest in the state after Visakhapatnam port and is the first port in the country to be built on a Public-private partnership basis (in 1996). It is operated by Kakinada Seaports Limited. Before the deep water port was built, the anchorage port was the largest of the forty minor ports operating in India. Currently both deep water port and older anchorage port co-exist. A shipyard is under construction, as a joint venture of Singapore-based Sembawang Shipyard Pvt. Ltd and Kakinada Seaports Ltd to provide vessel support services to ships plying around Kakinada port and on the East coast of India. Kakinada's principal exports now include seafood (prawns, shrimp, fish) and related products, agricultural products like rice, corn, oilmeals, processed food products, chemicals, iron ore, bauxite powder, and biofuel. Imports include chemicals, edible oils, and agricultural products (e.g. wheat and sugar). The deep water port handled a cargo of 13MT during 2009–10.LAURSAN&TUBRO,has choosen kakinada to build a ship yard with a worth of rupees 1000 crs.

    Industries

    Fertilizer

    Kakinada is often called the 'Fertilizer City' of Andhra Pradesh. The city is home to two fertiliser producers: Nagarjuna Fertilizers is the biggest urea manufacturer in coastal Andhra. Another company, Godavari Fertilizers owned by Murugappa Group, produces Diammonium Hydrogen Phosphate (DAP).

    Sugar

    The Murugappa Group-owned EID Parry (India) Ltd and Cargill International SA joint venture, Silk Road Sugars Pvt Ltd, has a port-based stand-alone sugar refinery in Kakinada with a refining capacity of 6 lakh tonnes. Reliance is also planning to set up a sugar mill. But due to scarcity of Gas, Silk road sugars pvt ltd is closed temporarily.

    Natural Gas and Petroleum

    Kakinada is the base for Oil and Natural Gas Corporation's Eastern Offshore Asset. Several oil companies have Kakinada as a transit point for oil and gasoline shipments. Baker Hughes and Schlumberger are examples of the field development companies working on natural gas fields offshore the city. The Krishna Godavari Basin is considered to be the largest natural gas basin in India and significant discoveries of oil and natural gas were made by Oil and Natural Gas Corporation (ONGC), Gujarat State Petroleum Corporation and Reliance, which has been producing around 60 mmscd of gas for the past two years from its prolific KG D6 block off the Kakinada coast. Reliance has an onshore terminal at Gadimoga village about 25 km from Kakinada to process and distribute gas to other parts of the country. Gujarat State Petroleum Corporation is also working on setting up a similar facility near Mallavaram village south of Kakinada. Reliance Gas Transportation Infrastructure Ltd (RGTIL) has built a 1,440 km pipeline from Kakinada to Bharuch (Gujarat) to transport 120 million cubic meters per day (mcmd) of natural gas from Krishna-Godavari fields owned by Reliance Industries across India to the west coast. In 2010, the Petroleum and Natural Gas Regulatory Board awarded the City Gas Distribution project for Kakinada city to Bhagyanagar Gas Limited, a consortium of GAIL and Hindustan Petroleum. The construction work is underway to supply gas to Kakinada city and the surrounding towns of Samalkot, Peddapuram and Pithapuram, thus making Kakinada the first city in Andhra Pradesh to get piped gas supply for domestic, commercial and industrial purposes along with Hyderabad and Vijayawada.

    Edible Oil Refineries and Biofuel Plants

    In 2002 several edible oil refineries established themselves in Kakinada and the refining capacity has touched 3000 tons per day. Kakinada port is facilitating the imports of crude palm oil, crude soyabean oil. Kakinada has an edible oil refining capacity of more than 3000 MTS per day. Major refineries are Acalmar Oils & Fats Limited (now, taken over by Adani Wilmar Ltd.), Ruchi Infrastructure, Nikhil Refineries Ltd, etc. The Vakalapudi Industrial park in Kakinada has attracted investments worth over US$ 10 million from bio-diesel companies such as Reliance Industries, Naturol Bioenergy and Universal Bio Fuel. Andhra Pradesh has entered into a formal agreement with Reliance Industries for Jatropha planting. The company has selected 200 acres (0.81 km2) of land at Kakinada to grow jatropha for high quality bio-diesel fuel.

    Power Generation

    There are several small and large power plants in and around Kakinada. Spectrum Power Generation Ltd. has a 208MW power plant at Kakinada. In fact, it was one of the first Independent Power Producer in the country. The company is planning to expand the capacity to 1350 MW in phases. Tenders for the first phase of expansion to the tune of 350 MW have been called for recently. A 220 MW Power Station (currently being scaled upwards to 2400 MW at a cost of Rs 10000 Cr) owned by Reliance Energy Limited, and a 464 MW Combined Cycle Power Plant by GVK group are under operation at Samalkota (Kakinada Rural). All these private power plants supply electricity to the state's transmission utility, AP TRANSCO, under a Power Purchase Agreement.

    Information Technology

    Kakinada is one of the 4 tier-II cities in Andhra Pradesh where Software Technology Parks of India (STPI) had set up a facility in 2007. Since the inception of the facility, several companies have started operations in this city and list is growing due to availability of highly educated workforce in the district. About 28 companies are currently operating in Kakinada with a total employee base of around 1200. Total turnover of IT/ITES from Kakinada is around Rs 15 Crore during the last fiscal year. Godavari IT Association of East and West Godavari districts (GITA) is an association of IT companies in the twin Godavari districts which is based out of the city. Some of the prominent IT companies that have set shop here are: Infotech Enterprises, a Hyderabad based multinational software company, Avineon Inc, an US based technology company that provides geospatial and engineering services, Firstobject Technologies, a prominent BPO firm. There are also several small to mid-size software companies that operate in Kakinada which include, Myfam Technologies,3One Technologies, TrewPort Technologies, Aaspire Technologies, Traceout Technologies, ForeTell Technologies Private Limited, Mythrii Solutions, Nyros Technologies, Meconzee InfoTech and Software Services, Easty Solutions. etc.

    Electronics

    Kakinada is home to Andhra Electronics Ltd., an electronic components manufacturing company, which started operations in 1977.

    Auto and Iron/Steel

    There are several auto and iron/steel ancillary industries in Kakinada, such as Sri Ramadas Motor Transport Limited and Sri Bhavani Castings Ltd.

    Rice Mills

    Several rice mills exist in and around Kakinada and some of the rice is exported to other countries.

    City

    With the recent growth in the industrial and commercial sectors, major hotels, multiplex theatres and shopping malls are just beginning to show up in the city.

    Retails, Entertainment and Attractions

    The city has many cinema theatres and multiplex theatres and constructing a new inox theatre at gudarigunta, a couple of parks, a cosmopolitan club apart from beaches and other natural scenic attractions. The city has many shoping malls M&M, Spencers, Nmart retails, more. Reliance, Sona, Raju Bhavan, Landmark, Planet Fashion & Laxons Baby World. The city has all new branded showrooms like Peter England, reebok, levis, basics life, woodland, club avis usa, jocky, flying machine, MEGA MART (the multi branded showroom), VILAN STYLO, H&A, K-Lounge (Killer), Lee, Wrangler, Pepe,white house,levis denizen,pan america, & the newly opened United Colors of Benetton at Kakinada Central Mall People here are just catching up with the mall culture and as such no major pan Indian mall can be seen here.
    Kakinada City was well planned, where the new comer can easily understand the City. Most of the Cinema Theatres can be seen on same road for which that road was named as Cinema Road.
    Surya Kala Mandir in the Cinema road is Famous Auditorium.

    Hotels

    The city is home to several three star and other lower range of hotels and resorts. Three-star hotels include Ishwarya Grand, Royal Park, Jaya Residency of Dasapalla Group, Oak Tree Hotel, Hotel ARKA,Venkey's Residency, THE PARK(proposed),city in(proposed) and the Paradigm Sarovar Portico (from India's third largest chain of hotels, The Sarovar Hotels and Resorts). Halycon times is a popular resort in the city.Surya residency which is in center of kakinada and The Green Park hotel chain is constructing a new hotel near ADB road. Kakinada is well known for the Famous Hotel 'Subbayya Hotel', it is famous for 'Butta Bhojanam' which satisfies with its taste & quantity. It's catering was spread around 200 KM radius for Functions and Marriages.

    Health care

    Kakinada has many health care facilities supported by both the government and private institutions. The major ones include the Government General Hospital (GGH), Apollo Hospitals, Christian Cancer Centre, Care Hospital, Sai Sudha Hospital, Sravani ENT Care, Trust Hospital, Star hospital, Safe Emergency Hospital, Sri Satya Sai Multispeciality Hospital and New Life Hospital. Kakinada also has famous eye hospitals like the 50 year old State of the art D. V. Raju Eye Hospital which has been serving the city and the district of East Godavari through 3 generations. Hospitals like Nayana eye care and kiran eye Hospital were established much later.

    Education

    Kakinada is a major educational hub fulfilling the growing educational demands of people in the state. The past decade has witnessed exponential growth and many residential colleges have been established to offer quality secondary education. There are also several professional colleges in and around the city offering courses in Engineering, Medical, Information Technology and Management at the graduate and postgraduate level.
    The Jawaharlal Nehru Technological University, Kakinada offers engineering courses and has a school of business, while Rangaraya Medical College is one of the best medical colleges in the state of Andhra Pradesh.
    Andhra University Post Graduate Centre (called A.U.M.S.N. PG Centre), established in November 1977, is another important college for higher learning in Kakinada. This University center is located between Kakinada Port – Samalkot ADB Road on a 50.93-acre (206,100 m2) campus in Thimmapuram. The campus is six kilometres from Kakinada Town Railway Station. There are many Schools with different boards like State, CBSE, ICSE. CBSE schools like Akshara, Ashram, Hamsavahini Vidyalaya, Subhaniketan, Nalanda, Kakinada Public School (KPS) etc. are prominent. Several state board private schools like Pragati Little public school, Aditya Public school, Pithapuram Rajas Govt Degree College (a), Ideal college of Arts and Sciences, M S N Degree College are also popular.
    There are many choultries in kakinada which provide free food facility for Poor Students throughout their Education. Famous Choultries are:
    1. Bangaru China Sobanadri (Office in the market near to Masjid Centre)
    2. Mutha Manikyam (Kalpana Centre)
    3. Mutha Sarvarayudu (kalpana Centre)
    4. Pynda Chalamaiah (Devalayam Street, Near Balaji Cheruvu)
    5. Mantripragada Choultry (Office in Mutta complex at Mantripragada street).
    These choultries take applications in the starting of the Academic year (June). Netha Varga Samkshema Sangham (Weavers Hostel):
    This hostel is located at Mantripragada Street which provides accommodation to Economically Backward students (Priority is given for students from Weavers Community) collecting only Maintenance Charges ( around Rs. 150/- per month). But due to lack of proper administration and funds this Hostel is in Pathetic situation and is about to close. For details of this hostel visit www.weavershostel.hpage.com
    Apart from this, there are some more hostels(BC Hostel, SC Hostel, OC Hostel) in Kakinada providing free accommodation, encouraging & supporting the Poor students to pursue their studies.
    Madireddy Library, Opposite to Sai Sudha Hospital near Balaji Cheruvu is a house of Books where Job aspirants can rely on it. It also houses Engineering Text Books, Diploma, Degree (all streams) & many other general useful books.

    Merger of Villages:

    There is a long time proposal to merge 37 villages around the city to form Greater Kakinada. This merging would make the population of Kakinada to rise up to 8 lakhs. And the Villages to be merged are:
    • Ramanayyapeta
    • Timmapuram
    • V Venkatapuram
    • Panduru
    • Nemam
    • Penumarthi
    • Tammavaram
    • Suryaraopeta
    • Vakalapudi
    • Valasapakala
    • Uppalanka
    • Gurajanapalli
    • Chollangi
    • Chollangipeta
    • Penuguduru
    • Korupalli
    • Nadakuduru
    • Z Bhavavaram
    • Aratlakatla
    • Goddatipalem
    • Kovvuru
    • Turangi
    • Koppavaram
    • Kakinada Medaline
    • Indrapalem
    • Chidiga
    • Kovvada
    • Repuru
    • Rameswaram
    • Ganganapalli
    • Swaminagar
    • S Atchutapuram
    • Madhavapatnam
    • Sarpavaram
    • Panasapadu
    • Atchampeta
    • Kakinada Revenue Village

    Tourism

    Though Kakinada is not known for tourism, it has some good places in and around to visit, like ancient temples, some beaches, mangrove forests and Godavari delta. The Union Territory of Yanam on the banks of River Godavari,25 km south of Kakinada, is making rapid strides in Tourism. A replica of the world famous Eiffel Tower, 100m in height, is being built there. AP Tourism is trying to promote the Konaseema region (30 km from Kakinada), into a tourism hub. Below is a list of places in and around Kakinada that may be of some interest to visitors.
    Annavaram Satyanarayana Swamy Temple, Andhra Pradesh's second richest temple, (40 km)
    Draksharama Shiva Temple (One of the five Pancharama Kshetras and aNational Heritage site), (25 km)
    Samalkot Shiva Temple (another one of the five Pancharama Kshetras and aNational Heritage site), (12 km)
    Sri Bhimeswaraswamy Vari Temple (Sri Chalukya Kumararama Temple, one of the five Pancharama Kshetras and a National Heritage site) (Samalkota, 10 km)
    Kukkuteshwara Swamy Temple at Pithapuram,(12 km)
    Kotipalli Kotilingeswara Temple, on the banks of the river Godavari, (30 km)
    Shri Bhavanarayana Swamy Temple (Sun God), Sarpavaram, Kakinada,(5 km)
    Coringa Wildlife Sanctuary, a part of River Godavari's estuary, (5 km)
    Hope Island, India, a sand spit formed in sea by River Godavari.(5 km offshore, from Vakalapudi beach)
    Konaseema, scenic locations of Godavari delta islands, (30 km)
    Kakinada-Uppada Beach (Vakalpudi Beach), (5 km) and
    Rajiv Gandhi Beach on the banks of the Godavari, Yanam, (25 km)
    Jain Temple, located in Main road

    Demographics

    As of 2011 census, Kakinada municipality had a population of 312,255 and the urban agglomeration had a population of 442,936. The sex ratio was 1046 females per 1000 males and 8.7% of the population were under six years old. Effective literacy was 81.23%; male literacy was 84.88% and female literacy was 77.76%.

    People

    People from Kakinada can easily be identified by their characteristic Godavari Telugu accent. They have gained a reputation for being hospitable, polite and cultured. People from Kakinada frequently uses a common suffix word 'andi' just like a word 'ji' in Hindi, which offers respect to the person corresponding to. The Godavari Telugu accent places emphasis on respecting elders and strangers. To achieve this, people of this region normally use the grammatical forms of Telugu that convey respect which is not found in Telugu usage in other parts of the Andhra Pradesh. The educated and the young understand English and use it as a mode of communication with people outside the state. Kakinada is a major educational center with several schools, colleges and universities. Many among the younger generation are migrating to the cities like Hyderabad, Visakhapatnam and out of the country in search of opportunities that meet their scale of ambition. However, there are significant parts of the society that have ridden the boom by expanding their businesses and investments. The local population is supplemented by immigrants who have left their villages to seek work and opportunity in this bustling city. People of Kakinada enjoy spending the hot summers in the shallow waters of Bay of Bengal. As tides are not intense and as the water is shallow people enjoy playing in the waters of Bay of Bengal. Devi Multiplex,[48] Janmabhoomi Park, Gandhinagar park and Vivekananda Park are other places people here love to hang out. Most of the people living in kakinada are belonging to middle class who enjoys by going to movies, parks, small hotels, roadside foods. Generally the people in this town are calm and decent. The temples are very pleasant, turning the people devotional. A varied number of cultures are followed here.

    Notable Residents

    Few among famous personalities from Kakinada:
    Chittajallu Srinivasa Rao (C.S.Rao) – actor, writer and director.
    C.Pullaiah – Telugu film director.
    Suryakantham (actress)
    Rao Gopal Rao (actor)
    Durgabai Deshmukh: (Freedom fighter, lawyer, social worker and politician)
    Kalpana Rai, female comedian of Telugu Film Industry was born in Kakinada

    Food

    East Godavari is famous for traditional Andhra cuisine and Kakinada is no different: pickles (aavakaaya) made from mangoes, vegetables (e.g. cauliflower aavakaaya), chicken, shrimp, mutton or even fish. Some people here swear by the pungent aroma and the lingering taste of dried fish (Endu Chepa) and shrimp (Endu Royya).
    This city is also famous for its unique Kakinada Kaaja, a sweet made from maida and dipped in sugar syrup. This sweet was very popular not only in Andhra but also in far away places like Bihar and U. P.[50] Kotiah Sweets (founded in 1900) is locally the most famous and possibly the earliest known maker of Kakinada Kaaja.
    Locals frequent the innumerable carts strategically located on populous street corners to purchase bhajis and a delicious mixture of onions, toasted rice, and sev (Pidatha Kindha Pappu).
    Kakinada is also one of the few regions in the entire Andhra Pradesh where Chekkarakeli aratipandu (banana) and Kothapalli kobbari maamidipandu (mango) are available. Kakinada is also famous for its delicious pesarattu, a breakfast or brunch item formed into crêpes from moong daal (pesara pappu), green chillies, ginger and cumin. These are sold in restaurants as well as street stalls. Pootarekulu is a sweet in coastal Andhra, made of thin sugar wafers.
    Kakinada is also famous for Udupi Vegetarian hotels. There are nearly half a dozen of the Udupi restaurant in the city, some of them provide even boarding & lodging.
    More recent food attractions include Yati foods and its restaurants at several locations in Kakinada. The Hyderabadi Dum Biryani recipe made at the Bhanugudi location is said to rival the famous Bawarchi biryani of Hyderabad, Other famous restaurants include Dakshin,Arali,E2,bhemas,seasons,unnat,aryan,spice,Haveli,surya residency and Varmas.

    Sports

    Cricket is the most popular game followed by badminton and athletics. The city is home to a number of local cricket teams participating in various district and zonal events. Kakinada has a cricket stadium used for Ranji Trophy matches. The East Godavari District Sports Authority has a vast sports campus in the city with many sporting facilities. An indoor stadium and a swimming pool are also located in this campus. Tennis is being taught to school and college students by KTA(Kakinada Tennis Academy) at the tennis courts of Rangaraya Medical College A roller skating rink is present at Vivekananda Park for skating enthusiasts.

    Health Hazard Criteria (Mandatory)

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    Appendix A TO §1910.1200—Health Hazard Criteria (Mandatory)
    A.0 GENERAL CLASSIFICATION CONSIDERATIONS
    A.0.1 Classification
    A.0.1.1 The term "hazard classification" is used to indicate that only the intrinsic hazardous properties of chemicals are considered. Hazard classification incorporates three steps:
    (a) identification of relevant data regarding the hazards of a chemical;

    (b) subsequent review of those data to ascertain the hazards associated with the chemical;

    (c) determination of whether the chemical will be classified as hazardous and the degree of hazard.
    A.0.1.2 For many hazard classes, the criteria are semi quantitative or qualitative and expert judgment is required to interpret the data for classification purposes.
    A.0.2 Available data, test methods and test data quality
    A.0.2.1 There is no requirement for testing chemicals.
    A.0.2.2 The criteria for determining health hazards are test method neutral, i.e., they do not specify particular test methods, as long as the methods are scientifically validated.
    A.0.2.3 The term "scientifically validated" refers to the process by which the reliability and the relevance of a procedure are established for a particular purpose. Any test that determines hazardous properties, which is conducted according to recognized scientific principles, can be used for purposes of a hazard determination for health hazards. Test conditions need to be standardized so that the results are reproducible with a given substance, and the standardized test yields "valid" data for defining the hazard class of concern.
    A.0.2.4 Existing test data are acceptable for classifying chemicals, although expert judgment also may be needed for classification purposes.
    A.0.2.5 The effect of a chemical on biological systems is influenced, by the physico-chemical properties of the substance and/or ingredients of the mixture and the way in which ingredient substances are biologically available. A chemical need not be classified when it can be shown by conclusive experimental data from scientifically validated test methods that the chemical is not biologically available.
    A.0.2.6 For classification purposes, epidemiological data and experience on the effects of chemicals on humans (e.g., occupational data, data from accident databases) shall be taken into account in the evaluation of human health hazards of a chemical.
    A.0.3 Classification based on weight of evidence
    A.0.3.1 For some hazard classes, classification results directly when the data satisfy the criteria. For others, classification of a chemical shall be determined on the basis of the total weight of evidence using expert judgment. This means that all available information bearing on the classification of hazard shall be considered together, including the results of valid in vitro tests, relevant animal data, and human experience such as epidemiological and clinical studies and well-documented case reports and observations.
    A.0.3.2 The quality and consistency of the data shall be considered. Information on chemicals related to the material being classified shall be considered as appropriate, as well as site of action and mechanism or mode of action study results. Both positive and negative results shall be considered together in a single weight-of-evidence determination.
    A.0.3.3 Positive effects which are consistent with the criteria for classification, whether seen in humans or animals, shall normally justify classification. Where evidence is available from both humans and animals and there is a conflict between the findings, the quality and reliability of the evidence from both sources shall be evaluated in order to resolve the question of classification. Reliable, good quality human data shall generally have precedence over other data. However, even well-designed and conducted epidemiological studies may lack a sufficient number of subjects to detect relatively rare but still significant effects, or to assess potentially confounding factors. Therefore, positive results from well-conducted animal studies are not necessarily negated by the lack of positive human experience but require an assessment of the robustness, quality and statistical power of both the human and animal data.
    A.0.3.4 Route of exposure, mechanistic information, and metabolism studies are pertinent to determining the relevance of an effect in humans. When such information raises doubt about relevance in humans, a lower classification may be warranted. When there is scientific evidence demonstrating that the mechanism or mode of action is not relevant to humans, the chemical should not be classified.
    A.0.3.5 Both positive and negative results are considered together in the weight of evidence determination. However, a single positive study performed according to good scientific principles and with statistically and biologically significant positive results may justify classification.
    A.0.4 Considerations for the classification of mixtures
    A.0.4.1 For most hazard classes, the recommended process of classification of mixtures is based on the following sequence:
    (a) Where test data are available for the complete mixture, the classification of the mixture will always be based on those data;

    (b) Where test data are not available for the mixture itself, the bridging principles designated in each health hazard chapter of this appendix shall be considered for classification of the mixture;

    (c) If test data are not available for the mixture itself, and the available information is not sufficient to allow application of the above-mentioned bridging principles, then the method(s) described in each chapter for estimating the hazards based on the information known will be applied to classify the mixture (e.g., application of cut-off values/concentration limits).
    A.0.4.2 An exception to the above order or precedence is made for Carcinogenicity, Germ Cell Mutagenicity, and Reproductive Toxicity. For these three hazard classes, mixtures shall be classified based upon information on the ingredient substances, unless on a case-by-case basis, justification can be provided for classifying based upon the mixture as a whole. See chapters A.5, A.6, and A.7 for further information on case-by-case bases.
    A.0.4.3 Use of cut-off values/concentration limits
    A.0.4.3.1 When classifying an untested mixture based on the hazards of its ingredients, cut-off values/concentration limits for the classified ingredients of the mixture are used for several hazard classes. While the adopted cut-off values/concentration limits adequately identify the hazard for most mixtures, there may be some that contain hazardous ingredients at lower concentrations than the specified cut-off values/concentration limits that still pose an identifiable hazard. There may also be cases where the cut-off value/concentration limit is considerably lower than the established non-hazardous level for an ingredient.
    A.0.4.3.2 If the classifier has information that the hazard of an ingredient will be evident (i.e., it presents a health risk) below the specified cut-off value/concentration limit, the mixture containing that ingredient shall be classified accordingly.
    A.0.4.3.3 In exceptional cases, conclusive data may demonstrate that the hazard of an ingredient will not be evident (i.e., it does not present a health risk) when present at a level above the specified cut-off value/concentration limit(s). In these cases the mixture may be classified according to those data. The data must exclude the possibility that the ingredient will behave in the mixture in a manner that would increase the hazard over that of the pure substance. Furthermore, the mixture must not contain ingredients that would affect that determination.
    A.0.4.4 Synergistic or antagonistic effects
    When performing an assessment in accordance with these requirements, the evaluator must take into account all available information about the potential occurrence of synergistic effects among the ingredients of the mixture. Lowering classification of a mixture to a less hazardous category on the basis of antagonistic effects may be done only if the determination is supported by sufficient data.
    A.0.5 Bridging principles for the classification of mixtures where test data are not available for the complete mixture
    A.0.5.1 Where the mixture itself has not been tested to determine its toxicity, but there are sufficient data on both the individual ingredients and similar tested mixtures to adequately characterize the hazards of the mixture, these data shall be used in accordance with the following bridging principles, subject to any specific provisions for mixtures for each hazard class. These principles ensure that the classification process uses the available data to the greatest extent possible in characterizing the hazards of the mixture.
    A.0.5.1.1 Dilution
    For mixtures classified in accordance with A.1 through A.10 of this Appendix, if a tested mixture is diluted with a diluent that has an equivalent or lower toxicity classification than the least toxic original ingredient, and which is not expected to affect the toxicity of other ingredients, then:
    (a) the new diluted mixture shall be classified as equivalent to the original tested mixture; or

    (b) for classification of acute toxicity in accordance with A.1 of this Appendix, paragraph A.1.3.6 (the additivity formula) shall be applied.
    A.0.5.1.2 Batching
    For mixtures classified in accordance with A.1 through A.10 of this Appendix, the toxicity of a tested production batch of a mixture can be assumed to be substantially equivalent to that of another untested production batch of the same mixture, when produced by or under the control of the same chemical manufacturer, unless there is reason to believe there is significant variation such that the toxicity of the untested batch has changed. If the latter occurs, a new classification is necessary.
    A.0.5.1.3 Concentration of mixtures
    For mixtures classified in accordance with A.1, A.2, A.3, A.8, A.9, or A.10 of this Appendix, if a tested mixture is classified in Category 1, and the concentration of the ingredients of the tested mixture that are in Category 1 is increased, the resulting untested mixture shall be classified in Category 1.
    A.0.5.1.4 Interpolation within one toxicity category
    For mixtures classified in accordance with A.1, A.2, A.3, A.8, A.9, or A.10 of this Appendix, for three mixtures (A, B and C) with identical ingredients, where mixtures A and B have been tested and are in the same toxicity category, and where untested mixture C has the same toxicologically active ingredients as mixtures A and B but has concentrations of toxicologically active ingredients intermediate to the concentrations in mixtures A and B, then mixture C is assumed to be in the same toxicity category as A and B.
    A.0.5.1.5 Substantially similar mixtures
    For mixtures classified in accordance with A.1 through A.10 of this Appendix, given the following set of conditions:
    (a) Where there are two mixtures: (i) A + B;
    (ii) C + B;

    (b) the concentration of ingredient B is essentially the same in both mixtures;

    (c) the concentration of ingredient A in mixture (i) equals that of ingredient C in mixture (ii);

    (d) and data on toxicity for A and C are available and substantially equivalent; i.e., they are in the same hazard category and are not expected to affect the toxicity of B; then
    If mixture (i) or (ii) is already classified based on test data, the other mixture can be assigned the same hazard category.
    A.0.5.1.6 Aerosols
    For mixtures classified in accordance with A.1, A.2, A.3, A.4, A.8, or A.9 of this Appendix, an aerosol form of a mixture shall be classified in the same hazard category as the tested, non-aerosolized form of the mixture, provided the added propellant does not affect the toxicity of the mixture when spraying.


    A.1 ACUTE TOXICITY
    A.1.1 Definition
    Acute toxicity refers to those adverse effects occurring following oral or dermal administration of a single dose of a substance, or multiple doses given within 24 hours, or an inhalation exposure of 4 hours.
    A.1.2 Classification criteria for substances
    A.1.2.1 Substances can be allocated to one of four toxicity categories based on acute toxicity by the oral, dermal or inhalation route according to the numeric cut-off criteria as shown in Table A.1.1. Acute toxicity values are expressed as (approximate) LD50 (oral, dermal) or LC50 (inhalation) values or as acute toxicity estimates (ATE). See the footnotes following Table A.1.1 for further explanation on the application of these values.
    Table A.1.1: Acute toxicity hazard categories and acute toxicity estimate (ATE) values
    defining the respective categories
    Exposure routeCategory 1Category 2Category 3Category 4
    Oral (mg/kg bodyweight)
    see:        Note (a)
                  Note (b)

    ≤ 5

    >5 and ≤ 50

    >50 and ≤ 300

    >300 and ≤ 2000
    Dermal (mg/kg bodyweight)
    see:        Note (a)
                  Note (b)

    ≤ 50

    >50 and ≤ 200

    >200 and ≤ 1000

    >1000 and ≤ 2000
    Inhalation - Gases (ppmV)
    see:        Note (a)
                  Note (b)
                  Note (c)

    ≤ 100

    >100 and ≤ 500

    >500 and ≤ 2500

    >2500 and ≤ 20000
    Inhalation - Vapors (mg/l)
    see:        Note (a)
                  Note (b)
                  Note (c)
                  Note (d)

    ≤ 0.5

    >0.5 and ≤ 2.0

    >2.0 and ≤ 10.0

    >10.0 and ≤ 20.0
    Inhalation – Dusts and Mists (mg/l)
    see:        Note (a)
                  Note (b)
                  Note (c)

    ≤ 0.05

    >0.05 and ≤ 0.5

    >0.5 and ≤ 1.0

    >1.0 and ≤ 5.0
    Note: Gas concentrations are expressed in parts per million per volume (ppmV).
    Notes to Table A.1.1:
    (a) The acute toxicity estimate (ATE) for the classification of a substance is derived using the LD50/LC50 where available;

    (b) The acute toxicity estimate (ATE) for the classification of a substance or ingredient in a mixture is derived using:
    (i) the LD50/LC50 where available. Otherwise,

    (ii) the appropriate conversion value from Table 1.2 that relates to the results of a range test, or

    (iii) the appropriate conversion value from Table 1.2 that relates to a classification category;
    (c) Inhalation cut-off values in the table are based on 4 hour testing exposures. Conversion of existing inhalation toxicity data which has been generated according to 1 hour exposure is achieved by dividing by a factor of 2 for gases and vapors and 4 for dusts and mists;

    (d) For some substances the test atmosphere will be a vapor which consists of a combination of liquid and gaseous phases. For other substances the test atmosphere may consist of a vapor which is nearly all the gaseous phase. In these latter cases, classification is based on ppmV as follows: Category 1 (100 ppmV), Category 2 (500 ppmV), Category 3 (2500 ppmV), Category 4 (20000 ppmV).

    The terms "dust", "mist" and "vapor" are defined as follows:
    (i) Dust: solid particles of a substance or mixture suspended in a gas (usually air);

    (ii) Mist: liquid droplets of a substance or mixture suspended in a gas (usually air);

    (iii) Vapor: the gaseous form of a substance or mixture released from its liquid or solid state.
    A.1.2.3 The preferred test species for evaluation of acute toxicity by the oral and inhalation routes is the rat, while the rat or rabbit are preferred for evaluation of acute dermal toxicity. Test data already generated for the classification of chemicals under existing systems should be accepted when reclassifying these chemicals under the harmonized system. When experimental data for acute toxicity are available in several animal species, scientific judgment should be used in selecting the most appropriate LD50 value from among scientifically validated tests.
    A.1.3 Classification criteria for mixtures
    A.1.3.1 The approach to classification of mixtures for acute toxicity is tiered, and is dependent upon the amount of information available for the mixture itself and for its ingredients. The flow chart of Figure A.1.1 indicates the process that must be followed:
    Figure A.1.1: Tiered approach to classification of mixtures for acute toxicity
    Figure A.1.1: Tiered approach to classification of mixtures for acute toxicity
    A.1.3.2 Classification of mixtures for acute toxicity may be carried out for each route of exposure, but is only required for one route of exposure as long as this route is followed (estimated or tested) for all ingredients and there is no relevant evidence to suggest acute toxicity by multiple routes. When there is relevant evidence of acute toxicity by multiple routes of exposure, classification is to be conducted for all appropriate routes of exposure. All available information shall be considered. The pictogram and signal word used shall reflect the most severe hazard category; and all relevant hazard statements shall be used.
    A.1.3.3 For purposes of classifying the hazards of mixtures in the tiered approach:
    (a) The "relevant ingredients" of a mixture are those which are present in concentrations ≥ 1% (weight/weight for solids, liquids, dusts, mists and vapors and volume/volume for gases). If there is reason to suspect that an ingredient present at a concentration < 1% will affect classification of the mixture for acute toxicity, that ingredient shall also be considered relevant. Consideration of ingredients present at a concentration < 1% is particularly important when classifying untested mixtures which contain ingredients that are classified in Category 1 and Category 2;

    (b) Where a classified mixture is used as an ingredient of another mixture, the actual or derived acute toxicity estimate (ATE) for that mixture is used when calculating the classification of the new mixture using the formulas in A.1.3.6.1 and A.1.3.6.2.4.

    (c) If the converted acute toxicity point estimates for all ingredients of a mixture are within the same category, then the mixture should be classified in that category.

    (d) When only range data (or acute toxicity hazard category information) are available for ingredients in a mixture, they may be converted to point estimates in accordance with Table A.1.2 when calculating the classification of the new mixture using the formulas in A.1.3.6.1 and A.1.3.6.2.4.
    A.1.3.4 Classification of mixtures where acute toxicity test data are available for the complete mixture
    Where the mixture itself has been tested to determine its acute toxicity, it is classified according to the same criteria as those used for substances, presented in Table A.1.1. If test data for the mixture are not available, the procedures presented below must be followed.
    A.1.3.5 Classification of mixtures where acute toxicity test data are not available for the complete mixture: bridging principles
    A.1.3.5.1 Where the mixture itself has not been tested to determine its acute toxicity, but there are sufficient data on both the individual ingredients and similar tested mixtures to adequately characterize the hazards of the mixture, these data will be used in accordance with the following bridging principles as found in paragraph A.0.5 of this Appendix: Dilution, Batching, Concentration of mixtures, Interpolation within one toxicity category, Substantially similar mixtures, and Aerosols.
    A.1.3.6 Classification of mixtures based on ingredients of the mixture (additivity formula)
    A.1.3.6.1 Data available for all ingredients
    The acute toxicity estimate (ATE) of ingredients is considered as follows:

    (a) Include ingredients with a known acute toxicity, which fall into any of the acute toxicity categories, or have an oral or dermal LD50 greater than 2000 but less than or equal to 5000 mg/kg body weight (or the equivalent dose for inhalation);

    (b) Ignore ingredients that are presumed not acutely toxic (e.g., water, sugar);

    (c) Ignore ingredients if the data available are from a limit dose test (at the upper threshold for Category 4 for the appropriate route of exposure as provided in Table A.1.1) and do not show acute toxicity.

    Ingredients that fall within the scope of this paragraph are considered to be ingredients with a known acute toxicity estimate (ATE). See note (b) to Table A.1.1 and paragraph A.1.3.3 for appropriate application of available data to the equation below, and paragraph A.1.3.6.2.4.
    The ATE of the mixture is determined by calculation from the ATE values for all relevant ingredients according to the following formula below for oral, dermal or inhalation toxicity:
    The formula for oral, dermal or inhalation toxicity
    where:
    Ci   =   concentration of ingredient i
    n ingredients and i is running from 1 to n
    ATEi   =   acute toxicity estimate of ingredient i.
    A.1.3.6.2 Data are not available for one or more ingredients of the mixture
    A.1.3.6.2.1 Where an ATE is not available for an individual ingredient of the mixture, but available information provides a derived conversion value, the formula in A.1.3.6.1 may be applied. This information may include evaluation of:
    (a) Extrapolation between oral, dermal and inhalation acute toxicity estimates. Such an evaluation requires appropriate pharmacodynamic and pharmacokinetic data;

    (b) Evidence from human exposure that indicates toxic effects but does not provide lethal dose data;

    (c) Evidence from any other toxicity tests/assays available on the substance that indicates toxic acute effects but does not necessarily provide lethal dose data; or

    (d) Data from closely analogous substances using structure/activity relationships.
    A.1.3.6.2.2 This approach requires substantial supplemental technical information, and a highly trained and experienced expert, to reliably estimate acute toxicity. If sufficient information is not available to reliably estimate acute toxicity, proceed to the provisions of A.1.3.6.2.3.
    A.1.3.6.2.3 In the event that an ingredient with unknown acute toxicity is used in a mixture at a concentration ≥ 1%, and the mixture has not been classified based on testing of the mixture as a whole, the mixture cannot be attributed a definitive acute toxicity estimate. In this situation the mixture is classified based on the known ingredients only. (Note: A statement that x percent of the mixture consists of ingredient(s) of unknown toxicity is required on the label and safety data sheet in such cases; see Appendix C, Allocation of Label Elements and Appendix D, Safety Data Sheets.)
    Where an ingredient with unknown acute toxicity is used in a mixture at a concentration ≥ 1%, and the mixture is not classified based on testing of the mixture as a whole, a statement that X% of the mixture consists of ingredient(s) of unknown acute toxicity is required on the label and safety data sheet in such cases; see Appendix C, Allocation of Label Elements and Appendix D, Safety Data Sheets.)
    A.1.3.6.2.4 If the total concentration of the relevant ingredient(s) with unknown acute toxicity is ≤ 10% then the formula presented in A.1.3.6.1 must be used. If the total concentration of the relevant ingredient(s) with unknown acute toxicity is < 10%, the formula presented in A.1.3.6.1 is corrected to adjust for the percentage of the unknown ingredient(s) as follows:
    The unknown ingredient(s)
    Table A.1.2: Conversion from experimentally obtained acute toxicity range values
    (or acute toxicity hazard categories) to acute toxicity point estimates for use in the formulas
    for the classification of mixtures

    Exposure routes
    Classification category or experimentally obtained
    acute toxicity range estimate
    Converted Acute Toxicity
    point estimate
    Oral
    (mg/kg bodyweight)
    0
    5
    50
    300
    < Category 1 ≤
    < Category 2 ≤
    < Category 3 ≤
    < Category 4 ≤
    5
    50
    300
    2000
    0.5
    5
    100
    500
    Dermal
    (mg/kg bodyweight)
    0
    50
    200
    1000
    < Category 1 ≤
    < Category 2 ≤
    < Category 3 ≤
    < Category 4 ≤
    50
    200
    1000
    2000
    5
    50
    300
    1100
    Gases
    (ppmV)
    0
    100
    500
    2500
    < Category 1 ≤
    < Category 2 ≤
    < Category 3 ≤
    < Category 4 ≤
    100
    500
    2500
    20000
    10
    100
    700
    4500
    Vapors
    (mg/l)
    0
    0.5
    2.0
    10.0
    < Category 1 ≤
    < Category 2 ≤
    < Category 3 ≤
    < Category 4 ≤
    0.5
    2.0
    10.0
    20.0
    0.05
    0.5
    3
    11
    Dust/mist
    (mg/l)
    0
    0.05
    0.5
    1.0
    < Category 1 ≤
    < Category 2 ≤
    < Category 3 ≤
    < Category 4 ≤
    0.05
    0.5
    1.0
    5.0
    0.005
    0.05
    0.5
    1.5
    Note: Gas concentrations are expressed in parts per million per volume (ppmV).


    A.2 SKIN CORROSION/IRRITATION
    A.2.1 Definitions and general considerations
    A.2.1.1 Skin corrosion is the production of irreversible damage to the skin; namely, visible necrosis through the epidermis and into the dermis, following the application of a test substance for up to 4 hours. Corrosive reactions are typified by ulcers, bleeding, bloody scabs, and, by the end of observation at 14 days, by discoloration due to blanching of the skin, complete areas of alopecia, and scars. Histopathology should be considered to evaluate questionable lesions.
    Skin irritation is the production of reversible damage to the skin following the application of a test substance for up to 4 hours.
    A.2.1.2 Skin corrosion/irritation shall be classified using a tiered approach as detailed in figure A.2.1. Emphasis shall be placed upon existing human data (See A.0.2.6), followed by other sources of information. Classification results directly when the data satisfy the criteria in this section. In case the criteria cannot be directly applied, classification of a substance or a mixture is made on the basis of the total weight of evidence (See A.0.3.1). This means that all available information bearing on the determination of skin corrosion/irritation is considered together, including the results of appropriate scientifically validated in-vitro tests, relevant animal data, and human data such as epidemiological and clinical studies and well-documented case reports and observations.
    A.2.2 Classification criteria for substances using animal test data
    A.2.2.1 Corrosion
    A.2.2.1.1 A corrosive substance is a chemical that produces destruction of skin tissue, namely, visible necrosis through the epidermis and into the dermis, in at least 1 of 3 tested animals after exposure up to a 4-hour duration. Corrosive reactions are typified by ulcers, bleeding, bloody scabs and, by the end of observation at 14 days, by discoloration due to blanching of the skin, complete areas of alopecia and scars. Histopathology should be considered to discern questionable lesions.
    A.2.2.1.2 Three sub-categories of Category 1 are provided in Table A.2.1, all of which shall be regulated as Category 1.
    Table A.2.1: Skin corrosion category and sub-categories
    Category 1: CorrosiveCorrosive sub-categoriesCorrosive in ≥ 1 of 3 animals
      ExposureObservation
     1A≤ 3 min≤ 1 h
    1B> 3 min ≤ 1 h≤ 14 days
    1C> 1 h ≤ 4 h≤ 14 days
    A.2.2.2 Irritation
    A.2.2.2.1 A single irritant category (Category 2) is presented in the Table A.2.2. The major criterion for the irritant category is that at least 2 tested animals have a mean score of ≥ 2.3 ≥ 4.0.
    Table A.2.2      Skin irritation category
     Criteria
    Irritant
    (Category 2)
    (1) Mean value of ≥ 2.3 ≥ 4.0 for erythema/eschar or for edema in at least 2 of 3 tested animals from gradings at 24, 48 and 72 hours after patch removal or, if reactions are delayed, from grades on 3 consecutive days after the onset of skin reactions; or
    (2) Inflammation that persists to the end of the observation period normally 14 days in at least 2 animals, particularly taking into account alopecia (limited area), hyperkeratosis, hyperplasia, and scaling; or
    (3) In some cases where there is pronounced variability of response among animals, with very definite positive effects related to chemical exposure in a single animal but less than the criteria above.
    A.2.2.2.2 Animal irritant responses within a test can be quite variable, as they are with corrosion. A separate irritant criterion accommodates cases when there is a significant irritant response but less than the mean score criterion for a positive test. For example, a substance might be designated as an irritant if at least 1 of 3 tested animals shows a very elevated mean score throughout the study, including lesions persisting at the end of an observation period of normally 14 days. Other responses could also fulfil this criterion. However, it should be ascertained that the responses are the result of chemical exposure. Addition of this criterion increases the sensitivity of the classification system.
    A.2.2.2.3. Reversibility of skin lesions is another consideration in evaluating irritant responses. When inflammation persists to the end of the observation period in 2 or more test animals, taking into consideration alopecia (limited area), hyperkeratosis, hyperplasia and scaling, then a chemical should be considered to be an irritant.
    A.2.3 Classification Criteria for Substances Using Other Data Elements
    A.2.3.1 Existing human and animal data including information from single or repeated exposure should be the first line of analysis, as they give information directly relevant to effects on the skin. If a substance is highly toxic by the dermal route, a skin corrosion/irritation study may not be practicable since the amount of test substance to be applied would considerably exceed the toxic dose and, consequently, would result in the death of the animals. When observations are made of skin corrosion/irritation in acute toxicity studies and are observed up through the limit dose, these data may be used for classification provided that the dilutions used and species tested are equivalent. In vitro alternatives that have been scientifically validated shall be used to make classification decisions. Solid substances (powders) may become corrosive or irritant when moistened or in contact with moist skin or mucous membranes. Likewise, pH extremes like ≤ 2 and ≥ 11.5 may indicate skin effects, especially when associated with significant buffering capacity. Generally, such substances are expected to produce significant effects on the skin. In the absence of any other information, a substance is considered corrosive (Skin Category 1) if it has a pH ≤ 2 or a pH ≥ 11.5. However, if consideration of alkali/acid reserve suggests the substance or mixture may not be corrosive despite the low or high pH value, then further evaluation may be necessary. In some cases enough information may be available from structurally related compounds to make classification decisions.
    A.2.3.2 A tiered approach to the evaluation of initial information shall be used (Figure A.2.1) recognizing that all elements may not be relevant in certain cases.
    A.2.3.3 The tiered approach explains how to organize information on a substance and to make a weight-of-evidence decision about hazard assessment and hazard classification.
    A.2.3.4 All the above information that is available on a substance shall be evaluated. Although information might be gained from the evaluation of single parameters within a tier, there is merit in considering the totality of existing information and making an overall weight of evidence determination. This is especially true when there is information available on some but not all parameters. Emphasis shall be placed upon existing human experience and data, followed by animal experience and testing data, followed by other sources of information, but case-by-case determinations are necessary.
    Figure A.2.1: Tiered evaluation of skin corrosion and irritation potential
    Figure A.2.1: Tiered evaluation of skin corrosion and irritation potential
    Notes to Figure A.2.1:
    1. Evidence of existing human or animal data may be derived from single or repeated exposure(s) in occupational, consumer, transportation, or emergency response scenarios; from ethically-conducted human clinical studies; or from purposely-generated data from animal studies conducted according to scientifically validated test methods (at present, there is no internationally accepted test method for human skin irritation testing).
    2. Classify in the appropriate harmonized category, as shown in Tables A.2.1 and A.2.2.
    3. Pre-existing animal data (e.g. from an acute dermal toxicity test or a sensitisation test) should be carefully reviewed to determine if sufficient skin corrosion/irritation evidence is available through other, similar information. For example, classification/categorization may be done on the basis of whether a chemical has or has not produced any skin irritation in an acute dermal toxicity test in animals at the limit dose, or produces very toxic effects in an acute dermal toxicity test in animals. In the latter case, the chemical would be classified as being very hazardous by the dermal route for acute toxicity, and it would be moot whether the chemical is also irritating or corrosive on the skin. It should be kept in mind in evaluating acute dermal toxicity information that the reporting of dermal lesions may be incomplete, testing and observations may be made on a species other than the rabbit, and species may differ in sensitivity in their responses.
    4. Evidence from studies using scientifically validated protocols with isolated human/animal tissues or other, non-tissue-based, though scientifically validated, protocols should be assessed. Examples of scientifically validated test methods for skin corrosion include OECD TG 430 (Transcutaneous Electrical Resistance Test (TER)), 431 (Human Skin Model Test), and 435 (Membrane Barrier Test Method). OECD TG 439 (Reconstructed Human Epidermis Test Method) is a scientifically validated in vitro test method for skin irritation.
    5. Measurement of pH alone may be adequate, but assessment of acid or alkali reserve (buffering capacity) would be preferable. Presently, there is no scientifically validated and internationally accepted method for assessing this parameter.
    6. All information that is available on a chemical should be considered and an overall determination made on the total weight of evidence. This is especially true when there is conflict in information available on some parameters. Professional judgment should be exercised in making such a determination.
    A.2.4 Classification criteria for mixtures
    A.2.4.1 Classification of mixtures when data are available for the complete mixture
    A.2.4.1.1 The mixture shall be classified using the criteria for substances (See A.2.3).
    A.2.4.2 Classification of mixtures when data are not available for the complete mixture: bridging principles
    A.2.4.2.1 Where the mixture itself has not been tested to determine its skin corrosion/irritation, but there are sufficient data on both the individual ingredients and similar tested mixtures to adequately characterize the hazards of the mixture, these data will be used in accordance with the following bridging principles, as found in paragraph A.0.5 of this Appendix: Dilution, Batching, Concentration of mixtures, Interpolation within one toxicity category, Substantially similar mixtures, and Aerosols.
    A.2.4.3 Classification of mixtures when data are available for all ingredients or only for some ingredients of the mixture
    A.2.4.3.1 For purposes of classifying the skin corrosion/irritation hazards of mixtures in the tiered approach:

    The "relevant ingredients" of a mixture are those which are present in concentrations ≥1% (weight/weight for solids, liquids, dusts, mists and vapors and volume/volume for gases.) If the classifier has reason to suspect that an ingredient present at a concentration <1% will affect classification of the mixture for skin corrosion/irritation, that ingredient shall also be considered relevant.
    A.2.4.3.2 In general, the approach to classification of mixtures as irritant or corrosive to skin when data are available on the ingredients, but not on the mixture as a whole, is based on the theory of additivity, such that each corrosive or irritant ingredient contributes to the overall irritant or corrosive properties of the mixture in proportion to its potency and concentration. A weighting factor of 10 is used for corrosive ingredients when they are present at a concentration below the concentration limit for classification with Category 1, but are at a concentration that will contribute to the classification of the mixture as an irritant. The mixture is classified as corrosive or irritant when the sum of the concentrations of such ingredients exceeds a cut-off value/concentration limit.
    A.2.4.3.3 Table A.2.3 below provides the cut-off value/concentration limits to be used to determine if the mixture is considered to be an irritant or a corrosive to the skin.
    A.2.4.3.4 Particular care shall be taken when classifying certain types of chemicals such as acids and bases, inorganic salts, aldehydes, phenols, and surfactants. The approach explained in A.2.4.3.1 and A.2.4.3.2 might not work given that many of such substances are corrosive or irritant at concentrations < 1%. For mixtures containing strong acids or bases the pH should be used as classification criteria since pH will be a better indicator of corrosion than the concentration limits of Table A.2.3. A mixture containing corrosive or irritant ingredients that cannot be classified based on the additivity approach shown in Table A.2.3, due to chemical characteristics that make this approach unworkable, should be classified as Skin Category 1 if it contains ≥ 1% of a corrosive ingredient and as Skin Category 2 when it contains ≥ 3% of an irritant ingredient. Classification of mixtures with ingredients for which the approach in Table A.2.3 does not apply is summarized in Table A.2.4 below.
    A.2.4.3.5 On occasion, reliable data may show that the skin corrosion/irritation of an ingredient will not be evident when present at a level above the generic concentration cut-off values mentioned in Tables A.2.3 and A.2.4. In these cases the mixture could be classified according to those data (See Use of cut-off values/concentration limits, paragraph A.0.4.3 of this Appendix).
    A.2.4.3.6 If there are data showing that (an) ingredient(s) may be corrosive or irritant at a concentration of < 1% (corrosive) or < 3% (irritant), the mixture shall be classified accordingly (See Use of cut-off values /concentration limits, paragraph A.0.4.3 of this Appendix).
    Table A.2.3: Concentration of ingredients of a mixture classified as skin Category 1 or 2
    that would trigger classification of the mixture as hazardous to skin (Category 1 or 2)


    Sum of ingredients
    classified as:
    Concentration triggering classification of a mixture as:
    Skin corrosiveSkin irritant
    Category 1Category 2
    Skin Category 1≥ 5%≥ 1% but < 5%
    Skin Category 2 ≥ 10%
    (10 x Skin Category 1) +
    Skin Category 2
     ≥ 10%
    Table A.2.4: Concentration of ingredients of a mixture for which the additivity approach
    does not apply, that would trigger classification of the mixture as hazardous to skin
    Ingredient:Concentration:Mixture classified as:
    Skin
    Acid with pH ≤ 2≥ 1%Category 1
    Base with pH ≥ 11.5≥ 1%Category 1
    Other corrosive (Category 1) ingredients for which additivity does not apply≥ 1%Category 1
    Other irritant (Category 2) ingredients for which additivity does not apply, including acids and bases≥ 3%Category 2


    A.3 SERIOUS EYE DAMAGE /EYE IRRITATION
    A.3.1 Definitions and general considerations
    A.3.1.1 Serious eye damage is the production of tissue damage in the eye, or serious physical decay of vision, following application of a test substance to the anterior surface of the eye, which is not fully reversible within 21 days of application.
    Eye irritation is the production of changes in the eye following the application of test substance to the anterior surface of the eye, which are fully reversible within 21 days of application.
    A.3.1.2 Serious eye damage/eye irritation shall be classified using a tiered approach as detailed in figure A.3.1. Emphasis shall be placed upon existing human data (See A.0.2.6), followed by animal data, followed by other sources of information. Classification results directly when the data satisfy the criteria in this section. In case the criteria cannot be directly applied, classification of a substance or a mixture is made on the basis of the total weight of evidence (See A.0.3.1). This means that all available information bearing on the determination of serious eye damage/eye irritation is considered together, including the results of appropriate scientifically validated in vitro tests, relevant animal data, and human data such as epidemiological and clinical studies and well-documented case reports and observations.
    A.3.2 Classification criteria for substances using animal test data
    A.3.2.1 Irreversible effects on the eye/serious damage to eyes (Category 1)
    A single hazard category is provided in Table A.3.1, for substances that have the potential to seriously damage the eyes. Category 1, irreversible effects on the eye, includes the criteria listed below. These observations include animals with grade 4 cornea lesions and other severe reactions (e.g. destruction of cornea) observed at any time during the test, as well as persistent corneal opacity, discoloration of the cornea by a dye substance, adhesion, pannus, and interference with the function of the iris or other effects that impair sight. In this context, persistent lesions are considered those which are not fully reversible within an observation period of normally 21 days. Category 1 also contains substances fulfilling the criteria of corneal opacity ≥ 3 and/or iritis > 1.5 detected in a Draize eye test with rabbits, because severe lesions like these usually do not reverse within a 21-day observation period.
    Table A.3.1: Irreversible eye effects
    A substance is classified as Serious Eye Damage Category 1 (irreversible effects on the eye) when it produces:

    (a) at least in one tested animal, effects on the cornea, iris or conjunctiva that are not expected to reverse or have not fully reversed within an observation period of normally 21 days; and/or

    (b) at least in 2 of 3 tested animals, a positive response of:
    (i) corneal opacity ≥ 3; and/or

    (ii) iritis > 1.5;

    calculated as the mean scores following grading at 24, 48 and 72 hours after instillation of the substance.
    A.3.2.2 Reversible effects on the eye (Category 2)
    A single category is provided in Table A.3.2 for substances that have the potential to induce reversible eye irritation.
    Table A.3.2: Reversible eye effects
    A substance is classified as Eye irritant Category 2A (irritating to eyes) when it produces in at least in 2 of 3 tested animals a positive response of:
    (i) corneal opacity ≥ 1; and/or

    (ii) iritis ≥ 1; and/or

    (iii) conjunctival redness ≥ 2; and/or

    (iv) conjunctival edema (chemosis) ≥ 2

    calculated as the mean scores following grading at 24, 48 and 72 hours after instillation of the substance, and which fully reverses within an observation period of normally 21 days.
    An eye irritant is considered mildly irritating to eyes (Category 2B) when the effects listed above are fully reversible within 7 days of observation.
    A.3.2.3 For those chemicals where there is pronounced variability among animal responses, this information may be taken into account in determining the classification.
    A.3.3 Classification Criteria for Substances Using Other Data Elements
    A.3.3.1 Existing human and animal data should be the first line of analysis, as they give information directly relevant to effects on the eye. Possible skin corrosion shall be evaluated prior to consideration of serious eye damage/eye irritation in order to avoid testing for local effects on eyes with skin corrosive substances. In vitro alternatives that have been scientifically validated and accepted shall be used to make classification decisions. Likewise, pH extremes like ≤ 2 and ≥ 11.5, may indicate serious eye damage, especially when associated with significant buffering capacity. Generally, such substances are expected to produce significant effects on the eyes. In the absence of any other information, a mixture/substance is considered to cause serious eye damage (Eye Category 1) if it has a pH ≤ 2 or ≥ 11.5. However, if consideration of acid/alkaline reserve suggests the substance may not have the potential to cause serious eye damage despite the low or high pH value, then further evaluation may be necessary. In some cases enough information may be available from structurally related compounds to make classification decisions.
    A.3.3.2 A tiered approach to the evaluation of initial information shall be used where applicable, recognizing that all elements may not be relevant in certain cases (Figure A.3.1).
    A.3.3.3 The tiered approach explains how to organize existing information on a substance and to make a weight-of-evidence decision, where appropriate, about hazard assessment and hazard classification.
    A.3.3.4 All the above information that is available on a substance shall be evaluated. Although information might be gained from the evaluation of single parameters within a tier, consideration should be given to the totality of existing information and making an overall weight of evidence determination. This is especially true when there is conflict in information available on some parameters.
    Figure A.3.1 Evaluation strategy for serious eye damage and eye irritation
    (See also Figure A.2.1)
    Figure A.3.1: Evaluation strategy for serious eye damage and eye irritation
    Notes to Figure A.3.1:
    1 Evidence of existing human or animal data may be derived from single or repeated exposure(s) in occupational, consumer, transportation, or emergency response scenarios; from ethically-conducted human clinical studies; or from purposely-generated data from animal studies conducted according to scientifically validated test methods. At present, there are no internationally accepted test methods for human skin or eye irritation testing.

    2 Classify in the appropriate harmonized category, as shown in Tables A.3.1 and A.3.2.

    3 Pre-existing animal data should be carefully reviewed to determine if sufficient skin or eye corrosion/irritation evidence is available through other, similar information.

    4 Evidence from studies using scientifically validated protocols with isolated human/animal tissues or other, non-tissue-based, though scientifically validated, protocols should be assessed. Examples of, scientifically validated test methods for identifying eye corrosives and severe irritants (i.e., Serious Eye Damage) include OECD TG 437 (Bovine Corneal Opacity and Permeability (BCOP)) and TG 438 (Isolated Chicken Eye). Positive test results from a scientifically validated in vitro test for skin corrosion would likely also lead to a conclusion to classify as causing Serious Eye Damage.

    5 Measurement of pH alone may be adequate, but assessment of acid or alkali reserve (buffering capacity) would be preferable.

    6 All information that is available on a chemical should be considered and an overall determination made on the total weight of evidence. This is especially true when there is conflict in information available on some parameters. The weight of evidence including information on skin irritation could lead to classification of eye irritation. It is recognized that not all skin irritants are eye irritants as well. Professional judgment should be exercised in making such a determination.
    A.3.4 Classification criteria for mixtures
    A.3.4.1 Classification of mixtures when data are available for the complete mixture
    A.3.4.1.1 The mixture will be classified using the criteria for substances
    A.3.4.1.2 Unlike other hazard classes, there are alternative tests available for skin corrosivity of certain types of chemicals that can give an accurate result for classification purposes, as well as being simple and relatively inexpensive to perform. When considering testing of the mixture, chemical manufacturers are encouraged to use a tiered weight of evidence strategy as included in the criteria for classification of substances for skin corrosion and serious eye damage and eye irritation to help ensure an accurate classification, as well as avoid unnecessary animal testing. In the absence of any other information, a mixture is considered to cause serious eye damage (Eye Category 1) if it has a pH ≤ 2 or ≥ 11.5. However, if consideration of acid/alkaline reserve suggests the substance or mixture may not have the potential to cause serious eye damage despite the low or high pH value, then further evaluation may be necessary.
    A.3.4.2 Classification of mixtures when data are not available for the complete mixture: bridging principles
    A.3.4.2.1 Where the mixture itself has not been tested to determine its skin corrosivity or potential to cause serious eye damage or eye irritation, but there are sufficient data on both the individual ingredients and similar tested mixtures to adequately characterize the hazards of the mixture, these data will be used in accordance with the following bridging principles, as found in paragraph A.0.5 of this Appendix: Dilution, Batching, Concentration of mixtures, Interpolation within one toxicity category, Substantially similar mixtures, and Aerosols.
    A.3.4.3 Classification of mixtures when data are available for all ingredients or only for some ingredients of the mixture
    A.3.4.3.1 For purposes of classifying the eye corrosion/irritation hazards of mixtures in the tiered approach:
    The "relevant ingredients" of a mixture are those which are present in concentrations ≥1% (weight/weight for solids, liquids, dusts, mists and vapors and volume/volume for gases.) If the classifier has reason to suspect that an ingredient present at a concentration <1% will affect classification of the mixture for eye corrosion/irritation, that ingredient shall also be considered relevant.
    A.3.4.3.2 In general, the approach to classification of mixtures as seriously damaging to the eye or eye irritant when data are available on the ingredients, but not on the mixture as a whole, is based on the theory of additivity, such that each corrosive or irritant ingredient contributes to the overall irritant or corrosive properties of the mixture in proportion to its potency and concentration. A weighting factor of 10 is used for corrosive ingredients when they are present at a concentration below the concentration limit for classification with Category 1, but are at a concentration that will contribute to the classification of the mixture as an irritant. The mixture is classified as seriously damaging to the eye or eye irritant when the sum of the concentrations of such ingredients exceeds a threshold cut-off value/concentration limit.
    A.3.4.3.3 Table A.3.3 provides the cut-off value/concentration limits to be used to determine if the mixture should be classified as seriously damaging to the eye or an eye irritant.
    A.3.4.3.4 Particular care must be taken when classifying certain types of chemicals such as acids and bases, inorganic salts, aldehydes, phenols, and surfactants. The approach explained in A.3.4.3.1 and A.3.4.3.2 might not work given that many of such substances are corrosive or irritant at concentrations < 1%. For mixtures containing strong acids or bases, the pH should be used as classification criteria (See A.3.4.1) since pH will be a better indicator of serious eye damage than the concentration limits of Table A.3.3. A mixture containing corrosive or irritant ingredients that cannot be classified based on the additivity approach applied in Table A.3.3 due to chemical characteristics that make this approach unworkable, should be classified as Eye Category 1 if it contains ≥ 1% of a corrosive ingredient and as Eye Category 2 when it contains ≥ 3% of an irritant ingredient. Classification of mixtures with ingredients for which the approach in Table A.3.3 does not apply is summarized in Table A.3.4.
    A.3.4.3.5 On occasion, reliable data may show that the reversible/irreversible eye effects of an ingredient will not be evident when present at a level above the generic cut-off values/concentration limits mentioned in Tables A.3.3 and A.3.4. In these cases the mixture could be classified according to those data (See also A.0.4.3 Use of cut-off values/concentration limits"). On occasion, when it is expected that the skin corrosion/irritation or the reversible/irreversible eye effects of an ingredient will not be evident when present at a level above the generic concentration/cut-off levels mentioned in Tables A.3.3 and A.3.4, testing of the mixture may be considered. In those cases, the tiered weight of evidence strategy should be applied as referred to in section A.3.3, Figure A.3.1 and explained in detail in this chapter.
    A.3.4.3.6 If there are data showing that (an) ingredient(s) may be corrosive or irritant at a concentration of < 1% (corrosive) or < 3% (irritant), the mixture should be classified accordingly (See also paragraph A.0.4.3, Use of cut-off values/concentration limits).
    Table A.3.3: Concentration of ingredients of a mixture classified as Skin Category 1 and/or
    Eye Category 1 or 2 that would trigger classification of the mixtures as hazardous to the eye


    Sum of ingredients classified as
    Concentration triggering classification of a mixture as
    Irreversible eye effectsReversible eye effects
    Category 1Category 2
    Eye or Skin Category 1≥ 3%≥ 1% but < 3%
    Eye Category 2 ≥ 10%
    (10 x Eye Category 1) + Eye Category 2 ≥ 10%
    Skin Category 1 + Eye Category 1≥ 3%≥ 1% but < 3%
    10 x (Skin Category 1 + Eye Category 1) + Eye Category 2 ≥ 10%
    Note: A mixture may be classified as Eye Category 2B in cases when all relevant ingredients are classified as Eye Category 2B.
    Table A.3.4: Concentration of ingredients of a mixture for which the additivity approach does
    not apply, that would trigger classification of the mixture as hazardous to the eye

    Ingredient

    Concentration
    Mixture classified as:
    Eye
    Acid with pH ≤ 2≥ 1%Category 1
    Base with pH ≥ 11.5≥ 1%Category 1
    Other corrosive (Category 1) ingredients for which additivity does not apply≥ 1%Category 1
    Other irritant (Category 2) ingredients for which additivity does not apply, including acids and bases≥ 3%Category 2


    A.4 RESPIRATORY OR SKIN SENSITIZATION
    A.4.1 Definitions and general considerations
    A.4.1.1 Respiratory sensitizer means a chemical that will lead to hypersensitivity of the airways following inhalation of the chemical.
    Skin sensitizer means a chemical that will lead to an allergic response following skin contact.
    A.4.1.2 For the purpose of this chapter, sensitization includes two phases: the first phase is induction of specialized immunological memory in an individual by exposure to an allergen. The second phase is elicitation, i.e., production of a cell-mediated or antibody-mediated allergic response by exposure of a sensitized individual to an allergen.
    A.4.1.3 For respiratory sensitization, the pattern of induction followed by elicitation phases is shared in common with skin sensitization. For skin sensitization, an induction phase is required in which the immune system learns to react; clinical symptoms can then arise when subsequent exposure is sufficient to elicit a visible skin reaction (elicitation phase). As a consequence, predictive tests usually follow this pattern in which there is an induction phase, the response to which is measured by a standardized elicitation phase, typically involving a patch test. The local lymph node assay is the exception, directly measuring the induction response. Evidence of skin sensitization in humans normally is assessed by a diagnostic patch test.
    A.4.1.4 Usually, for both skin and respiratory sensitization, lower levels are necessary for elicitation than are required for induction.
    A.4.1.5 The hazard class "respiratory or skin sensitization" is differentiated into:
    (a) Respiratory sensitization; and

    (b) Skin sensitization
    A.4.2 Classification criteria for substances
    A.4.2.1 Respiratory sensitizers
    A.4.2.1.1 Hazard categories
    A.4.2.1.1.1 Effects seen in either humans or animals will normally justify classification in a weight of evidence approach for respiratory sensitizers. Substances may be allocated to one of the two sub-categories 1A or 1B using a weight of evidence approach in accordance with the criteria given in Table A.4.1 and on the basis of reliable and good quality evidence from human cases or epidemiological studies and/or observations from appropriate studies in experimental animals.
    A.4.2.1.1.2 Where data are not sufficient for sub-categorization, respiratory sensitizers shall be classified in Category 1.
    Table A.4.1: Hazard category and sub-categories for respiratory sensitizers
    Category 1:Respiratory sensitizer
     A substance is classified as a respiratory sensitizer
    (a) if there is evidence in humans that the substance can lead to specific respiratory hypersensitivity and/or
    (b) if there are positive results from an appropriate animal test.
      Sub-category 1A:Substances showing a high frequency of occurrence in humans; or a probability of occurrence of a high sensitization rate in humans based on animal or other tests.1 Severity of reaction may also be considered.
      Sub-category 1B:Substances showing a low to moderate frequency of occurrence in humans; or a probability of occurrence of a low to moderate sensitization rate in humans based on animal or other tests.1 Severity of reaction may also be considered.
    A.4.2.1.2 Human evidence
    A.4.2.1.2.1 Evidence that a substance can lead to specific respiratory hypersensitivity will normally be based on human experience. In this context, hypersensitivity is normally seen as asthma, but other hypersensitivity reactions such as rhinitis/conjunctivitis and alveolitis are also considered. The condition will have the clinical character of an allergic reaction. However, immunological mechanisms do not have to be demonstrated.
    A.4.2.1.2.2 When considering the human evidence, it is necessary that in addition to the evidence from the cases, the following be taken into account:
    (a) the size of the population exposed;

    (b) the extent of exposure.
    A.4.2.1.2.3 The evidence referred to above could be:
    (a) clinical history and data from appropriate lung function tests related to exposure to the substance, confirmed by other supportive evidence which may include:
    (i) in vivo immunological test (e.g., skin prick test);

    (ii) in vitro immunological test (e.g., serological analysis);

    (iii) studies that may indicate other specific hypersensitivity reactions where immunological mechanisms of action have not been proven, e.g., repeated low-level irritation, pharmacologically mediated effects;

    (iv) a chemical structure related to substances known to cause respiratory hypersensitivity;
    (b) data from positive bronchial challenge tests with the substance conducted according to accepted guidelines for the determination of a specific hypersensitivity reaction.
    A.4.2.1.2.4 Clinical history should include both medical and occupational history to determine a relationship between exposure to a specific substance and development of respiratory hypersensitivity. Relevant information includes aggravating factors both in the home and workplace, the onset and progress of the disease, family history and medical history of the patient in question. The medical history should also include a note of other allergic or airway disorders from childhood and smoking history.
    A.4.2.1.2.5 The results of positive bronchial challenge tests are considered to provide sufficient evidence for classification on their own. It is, however, recognized that in practice many of the examinations listed above will already have been carried out.
    A.4.2.1.3 Animal studies
    A.4.2.1.3.1 Data from appropriate animal studies which may be indicative of the potential of a substance to cause sensitization by inhalation in humans may include:
    (a) measurements of Immunoglobulin E (IgE) and other specific immunological parameters, for example in mice

    (b) specific pulmonary responses in guinea pigs.
    A.4.2.2 Skin sensitizers
    A.4.2.2.1 Hazard categories
    A.4.2.2.1.1 Effects seen in either humans or animals will normally justify classification in a weight of evidence approach for skin sensitizers. Substances may be allocated to one of the two sub-categories 1A or 1B using a weight of evidence approach in accordance with the criteria given in Table A.4.2 and on the basis of reliable and good quality evidence from human cases or epidemiological studies and/or observations from appropriate studies in experimental animals according to the guidance values provided in A.4.2.2.2.1 and A.4.2.2.3.2 for sub-category 1A and in A.4.2.2.2.2 and A.4.2.2.3.3 for sub-category 1B.
    A.4.2.2.1.2 Where data are not sufficient for sub-categorization, skin sensitizers shall be classified in Category 1.
    Table A.4.2: Hazard category and sub-categories for skin sensitizers
    Category 1:Skin sensitizer
     A substance is classified as a skin sensitizer
    (a) if there is evidence in humans that the substance can lead to sensitization by skin contact in a substantial number of persons, or
    (b) if there are positive results from an appropriate animal test.
      Sub-category 1A:Substances showing a high frequency of occurrence in humans and/or a high potency in animals can be presumed to have the potential to produce significant sensitization in humans. Severity of reaction may also be considered.
      Sub-category 1B:Substances showing a low to moderate frequency of occurrence in humans and/or a low to moderate potency in animals can be presumed to have the potential to produce sensitization in humans. Severity of reaction may also be considered.
    A.4.2.2.2 Human evidence
    A.4.2.2.2.1 Human evidence for sub-category 1A may include:
    (a) positive responses at ≤ 500 µg/cm2 (Human Repeat Insult Patch Test (HRIPT), Human Maximization Test (HMT) – induction threshold);

    (b) diagnostic patch test data where there is a relatively high and substantial incidence of reactions in a defined population in relation to relatively low exposure;

    (c) other epidemiological evidence where there is a relatively high and substantial incidence of allergic contact dermatitis in relation to relatively low exposure.
    A.4.2.2.2.2 Human evidence for sub-category 1B may include:
    (a) positive responses at > 500 µg/cm2 (HRIPT, HMT – induction threshold);

    (b) diagnostic patch test data where there is a relatively low but substantial incidence of reactions in a defined population in relation to relatively high exposure;

    (c) other epidemiological evidence where there is a relatively low but substantial incidence of allergic contact dermatitis in relation to relatively high exposure.
    A.4.2.2.3 Animal studies
    A.4.2.2.3.1 For Category 1, when an adjuvant type test method for skin sensitization is used, a response of at least 30% of the animals is considered as positive. For a non-adjuvant Guinea pig test method a response of at least 15% of the animals is considered positive. For Category 1, a stimulation index of three or more is considered a positive response in the local lymph node assay.
    A.4.2.2.3.2 Animal test results for sub-category 1A can include data with values indicated in Table A.4.3 below:
    Table A.4.3: Animal test results for sub-category 1A
    AssayCriteria
    Local lymph node assayEC3 value ≤ 2%
    Guinea pig maximization test≥ 30% responding at ≤ 0.1% intradermal induction dose or
    ≥ 60% responding at > 0.1% to ≤ 1% intradermal induction dose
    Buehler assay≥ 15% responding at ≤ 0.2% topical induction dose or
    ≥ 60% responding at > 0.2% to ≤ 20% topical induction dose
    Note: EC3 refers to the estimated concentration of test chemical required to induce a stimulation index of 3 in the local lymph node assay.
    A.4.2.2.3.3 Animal test results for sub-category 1B can include data with values indicated in Table A.4.4 below:
    Table A.4.4: Animal test results for sub-category 1B
    AssayCriteria
    Local lymph node assayEC3 value > 2%
    Guinea pig maximization test≥ 30% to < 60% responding at > 0.1% to ≤ 1% intradermal induction dose or
    ≥ 30% responding at > 1% intradermal induction dose
    Buehler assay≥ 15% to < 60% responding at > 0.2% to ≤ 20% topical induction dose or
    ≥ 15% responding at > 20% topical induction dose
    Note: EC3 refers to the estimated concentration of test chemical required to induce a stimulation index of 3 in the local lymph node assay.
    A.4.2.2.4 Specific considerations
    A.4.2.2.4.1 For classification of a substance, evidence shall include one or more of the following using a weight of evidence approach:
    (a) Positive data from patch testing, normally obtained in more than one dermatology clinic;

    (b) Epidemiological studies showing allergic contact dermatitis caused by the substance. Situations in which a high proportion of those exposed exhibit characteristic symptoms are to be looked at with special concern, even if the number of cases is small;

    (c) Positive data from appropriate animal studies;

    (d) Positive data from experimental studies in man (See paragraph A.0.2.6 of this Appendix);

    (e) Well documented episodes of allergic contact dermatitis, normally obtained in more than one dermatology clinic;

    (f) Severity of reaction.
    A.4.2.2.4.2 Evidence from animal studies is usually much more reliable than evidence from human exposure. However, in cases where evidence is available from both sources, and there is conflict between the results, the quality and reliability of the evidence from both sources must be assessed in order to resolve the question of classification on a case-by-case basis. Normally, human data are not generated in controlled experiments with volunteers for the purpose of hazard classification but rather as part of risk assessment to confirm lack of effects seen in animal tests. Consequently, positive human data on skin sensitization are usually derived from case-control or other, less defined studies. Evaluation of human data must, therefore, be carried out with caution as the frequency of cases reflect, in addition to the inherent properties of the substances, factors such as the exposure situation, bioavailability, individual predisposition and preventive measures taken. Negative human data should not normally be used to negate positive results from animal studies. For both animal and human data, consideration should be given to the impact of vehicle.
    A.4.2.2.4.3 If none of the above-mentioned conditions are met, the substance need not be classified as a skin sensitizer. However, a combination of two or more indicators of skin sensitization, as listed below, may alter the decision. This shall be considered on a case-by-case basis.
    (a) Isolated episodes of allergic contact dermatitis;

    (b) Epidemiological studies of limited power, e.g., where chance, bias or confounders have not been ruled out fully with reasonable confidence;

    (c) Data from animal tests, performed according to existing guidelines, which do not meet the criteria for a positive result described in A.4.2.2.3, but which are sufficiently close to the limit to be considered significant;

    (d) Positive data from non-standard methods;

    (e) Positive results from close structural analogues.
    A.4.2.2.4.4 Immunological contact urticaria
    A.4.2.2.4.4.1 Substances meeting the criteria for classification as respiratory sensitizers may, in addition, cause immunological contact urticaria. Consideration shall be given to classifying these substances as skin sensitizers.
    A.4.2.2.4.4.2 Substances which cause immunological contact urticaria without meeting the criteria for respiratory sensitizers shall be considered for classification as skin sensitizers.
    A.4.2.2.4.4.3 There is no recognized animal model available to identify substances which cause immunological contact urticaria. Therefore, classification will normally be based on human evidence, similar to that for skin sensitization.
    A.4.3 Classification criteria for mixtures
    A.4.3.1 Classification of mixtures when data are available for the complete mixture
    When reliable and good quality evidence, as described in the criteria for substances, from human experience or appropriate studies in experimental animals, is available for the mixture, then the mixture shall be classified by weight of evidence evaluation of these data. Care must be exercised in evaluating data on mixtures that the dose used does not render the results inconclusive.
    A.4.3.2 Classification of mixtures when data are not available for the complete mixture: bridging principles
    A.4.3.2.1 Where the mixture itself has not been tested to determine its sensitizing properties, but there are sufficient data on both the individual ingredients and similar tested mixtures to adequately characterize the hazards of the mixture, these data will be used in accordance with the following agreed bridging principles as found in paragraph A.0.5 of this Appendix: Dilution, Batching, Concentration of mixtures, Interpolation, Substantially similar mixtures, and Aerosols.
    A.4.3.3 Classification of mixtures when data are available for all ingredients or only for some ingredients of the mixture
    The mixture shall be classified as a respiratory or skin sensitizer when at least one ingredient has been classified as a respiratory or skin sensitizer and is present at or above the appropriate cut-off value/concentration limit for the specific endpoint as shown in Table A.4.5.
    Table A.4.5: Cut-off values/concentration limits of ingredients of a mixture classified as either
    respiratory sensitizers or skin sensitizers that would trigger classification of the mixture





    Ingredient classified as:
    Cut-off values/concentration limits
    triggering classification of a mixture as:
    Respiratory Sensitizer
    Category 1
    Skin Sensitizer
    Category 1
    Solid/LiquidGasAll physical states
    Respiratory Sensitizer
    Category 1
    ≥ 0.1%≥ 0.1% 
    Respiratory Sensitizer
    Sub-category 1A
    ≥ 0.1%≥ 0.1% 
    Respiratory Sensitizer
    Sub-category 1B
    ≥ 0.1%≥ 0.2% 
    Skin Sensitizer
    Category 1
      ≥ 0.1%
    Skin Sensitizer
    Sub-category 1A
      ≥ 0.1%
    Skin Sensitizer
    Sub-category 1B
      ≥ 1.0%


    A.5 GERM CELL MUTAGENICITY
    A.5.1 Definitions and general considerations
    A.5.1.1 A mutation is defined as a permanent change in the amount or structure of the genetic material in a cell. The term mutation applies both to heritable genetic changes that may be manifested at the phenotypic level and to the underlying DNA modifications when known (including, for example, specific base pair changes and chromosomal translocations). The term mutagenic and mutagen will be used for agents giving rise to an increased occurrence of mutations in populations of cells and/or organisms.
    A.5.1.2 The more general terms genotoxic and genotoxicity apply to agents or processes which alter the structure, information content, or segregation of DNA, including those which cause DNA damage by interfering with normal replication processes, or which in a non-physiological manner (temporarily) alter its replication. Genotoxicity test results are usually taken as indicators for mutagenic effects.
    A.5.1.3 This hazard class is primarily concerned with chemicals that may cause mutations in the germ cells of humans that can be transmitted to the progeny. However, mutagenicity/genotoxicity tests in vitro and in mammalian somatic cells in vivo are also considered in classifying substances and mixtures within this hazard class.
    A.5.2 Classification criteria for substances
    A.5.2.1 The classification system provides for two different categories of germ cell mutagens to accommodate the weight of evidence available. The two-category system is described in the Figure A.5.1.
    Figure A.5.1: Hazard categories for germ cell mutagens
    CATEGORY 1:


    Category 1A:


    Category 1B:








    CATEGORY 2:
    Substances known to induce heritable mutations or to be regarded as if they induce heritable mutations in the germ cells of humans

    Substances known to induce heritable mutations in germ cells of humans

    Positive evidence from human epidemiological studies.

    Substances which should be regarded as if they induce heritable mutations in the germ cells of humans
    (a) Positive result(s) from in vivo heritable germ cell mutagenicity tests in mammals; or
    (b) Positive result(s) from in vivo somatic cell mutagenicity tests in mammals, in combination with some evidence that the substance has potential to cause mutations to germ cells. This supporting evidence may, for example, be derived from mutagenicity/genotoxicity tests in germ cells in vivo, or by demonstrating the ability of the substance or its metabolite(s) to interact with the genetic material of germ cells; or
    (c) Positive results from tests showing mutagenic effects in the germ cells of humans, without demonstration of transmission to progeny; for example, an increase in the frequency of aneuploidy in sperm cells of exposed people.

    Substances which cause concern for humans owing to the possibility that they may induce heritable mutations in the germ cells of humans
    Positive evidence obtained from experiments in mammals and/or in some cases from in vitro experiments, obtained from:
    (a) Somatic cell mutagenicity tests in vivo, in mammals; or
    (b) Other in vivo somatic cell genotoxicity tests which are supported by positive results from in vitro mutagenicity assays.
    Note: Substances which are positive in in vitro mammalian mutagenicity assays, and which also show chemical structure activity relationship to known germ cell mutagens, should be considered for classification as Category 2 mutagens.
    A.5.2.2 Specific considerations for classification of substances as germ cell mutagens:
    A.5.2.2.1 To arrive at a classification, test results are considered from experiments determining mutagenic and/or genotoxic effects in germ and/or somatic cells of exposed animals. Mutagenic and/or genotoxic effects determined in in vitro tests shall also be considered.
    A.5.2.2.2 The system is hazard based, classifying chemicals on the basis of their intrinsic ability to induce mutations in germ cells. The scheme is, therefore, not meant for the (quantitative) risk assessment of chemical substances.
    A.5.2.2.3 Classification for heritable effects in human germ cells is made on the basis of scientifically validated tests. Evaluation of the test results shall be done using expert judgment and all the available evidence shall be weighed for classification.
    A.5.2.2.4 The classification of substances shall be based on the total weight of evidence available, using expert judgment. In those instances where a single well-conducted test is used for classification, it shall provide clear and unambiguously positive results. The relevance of the route of exposure used in the study of the substance compared to the route of human exposure should also be taken into account.
    A.5.3 Classification criteria for mixtures
    A.5.3.1 Classification of mixtures when data are available for all ingredients or only for some ingredients of the mixture
    A.5.3.1.1 Classification of mixtures shall be based on the available test data for the individual ingredients of the mixture using cut-off values/concentration limits for the ingredients classified as germ cell mutagens.
    A.5.3.1.2 The mixture will be classified as a mutagen when at least one ingredient has been classified as a Category 1A, Category 1B or Category 2 mutagen and is present at or above the appropriate cut-off value/concentration limit as shown in Table A.5.1 below for Category 1 and 2 respectively.
    Table A.5.1: Cut-off values/concentration limits of ingredients of a mixture classified as
    germ cell mutagens that would trigger classification of the mixture


    Ingredient classified as:
    Cut-off/concentration limits triggering classification of a mixture as:
    Category 1 mutagenCategory 2 mutagen
    Category 1A/B mutagen≥ 0.1 %-
    Category 2 mutagen-≥ 1.0 %
    Note: The cut-off values/concentration limits in the table above apply to solids and liquids (w/w units) as well as gases (v/v units).
    A.5.3.2 Classification of mixtures when data are available for the mixture itself
    The classification may be modified on a case-by-case basis based on the available test data for the mixture as a whole. In such cases, the test results for the mixture as a whole must be shown to be conclusive taking into account dose and other factors such as duration, observations and analysis (e.g. statistical analysis, test sensitivity) of germ cell mutagenicity test systems.
    A.5.3.3 Classification of mixtures when data are not available for the complete mixture: bridging principles
    A.5.3.3.1 Where the mixture itself has not been tested to determine its germ cell mutagenicity hazard, but there are sufficient data on both the individual ingredients and similar tested mixtures to adequately characterize the hazards of the mixture, these data will be used in accordance with the following bridging principles as found in paragraph A.0.5 of this Appendix: Dilution, Batching, and Substantially similar mixtures.
    A.5.4 Examples of scientifically validated test methods:
    A.5.4.1 Examples of in vivo heritable germ cell mutagenicity tests are:
    (a) Rodent dominant lethal mutation test (OECD 478)

    (b) Mouse heritable translocation assay (OECD 485)

    (c) Mouse specific locus test
    A.5.4.2 Examples of in vivo somatic cell mutagenicity tests are:
    (a) Mammalian bone marrow chromosome aberration test (OECD 475)

    (b) Mouse spot test (OECD 484)

    (c) Mammalian erythrocyte micronucleus test (OECD 474)
    A.5.4.3 Examples of mutagenicity/genotoxicity tests in germ cells are:
    (a) Mutagenicity tests:

    (i) Mammalian spermatogonial chromosome aberration test (OECD 483)

    (ii) Spermatid micronucleus assay
    (b) Genotoxicity tests:

    (i) Sister chromatid exchange analysis in spermatogonia

    (ii) Unscheduled DNA synthesis test (UDS) in testicular cells
    A.5.4.4 Examples of genotoxicity tests in somatic cells are:
    (a) Liver Unscheduled DNA Synthesis (UDS) in vivo (OECD 486)

    (b) Mammalian bone marrow Sister Chromatid Exchanges (SCE)
    A.5.4.5 Examples of in vitro mutagenicity tests are:
    (a) In vitro mammalian chromosome aberration test (OECD 473)

    (b) In vitro mammalian cell gene mutation test (OECD 476)

    (c) Bacterial reverse mutation tests (OECD 471)
    A.5.4.6 As new, scientifically validated tests arise, these may also be used in the total weight of evidence to be considered.


    A.6 CARCINOGENICITY
    A.6.1 Definitions
    Carcinogen means a substance or a mixture of substances which induce cancer or increase its incidence. Substances and mixtures which have induced benign and malignant tumors in well-performed experimental studies on animals are considered also to be presumed or suspected human carcinogens unless there is strong evidence that the mechanism of tumor formation is not relevant for humans.
    Classification of a substance or mixture as posing a carcinogenic hazard is based on its inherent properties and does not provide information on the level of the human cancer risk which the use of the substance or mixture may represent.
    A.6.2 Classification criteria for substances
    A.6.2.1 For the purpose of classification for carcinogenicity, substances are allocated to one of two categories based on strength of evidence and additional weight of evidence considerations. In certain instances, route-specific classification may be warranted.
    Figure A.6.1: Hazard categories for carcinogens
    CATEGORY 1:




    Category 1A:

    Category 1B:









    CATEGORY 2:





    Other considerations:
    Known or presumed human carcinogens
    The classification of a substance as a Category 1 carcinogen is done on the basis of epidemiological and/or animal data. This classification is further distinguished on the basis of whether the evidence for classification is largely from human data (Category 1A) or from animal data (Category 1B):

    Known to have carcinogenic potential for humans. Classification in this category is largely based on human evidence.

    Presumed to have carcinogenic potential for humans. Classification in this category is largely based on animal evidence.
    The classification of a substance in Category 1A and 1B is based on strength of evidence together with weight of evidence considerations (See paragraph A.6.2.5). Such evidence may be derived from:
    - human studies that establish a causal relationship between human exposure to a substance and the development of cancer (known human carcinogen); or
    - animal experiments for which there is sufficient evidence to demonstrate animal carcinogenicity (presumed human carcinogen).
    In addition, on a case by case basis, scientific judgment may warrant a decision of presumed human carcinogenicity derived from studies showing limited evidence of carcinogenicity in humans together with limited evidence of carcino¬genicity in experimental animals.

    Suspected human carcinogens
    The classification of a substance in Category 2 is done on the basis of evidence obtained from human and/or animal studies, but which is not sufficiently convincing to place the substance in Category 1A or B. This classification is based on strength of evidence together with weight of evidence considerations (See paragraph A.6.2.5). Such evidence may be from either limited evidence of carcinogenicity in human studies or from limited evidence of carcinogenicity in animal studies.

    Where the weight of evidence for the carcinogenicity of a substance does not meet the above criteria, any positive study conducted in accordance with established scientific principles, and which reports statistically significant findings regarding the carcinogenic potential of the substance, must be noted on the safety data sheet.
    A.6.2.2 Classification as a carcinogen is made on the basis of evidence from reliable and acceptable methods, and is intended to be used for substances which have an intrinsic property to produce such toxic effects. The evaluations are to be based on all existing data, peer-reviewed published studies and additional data accepted by regulatory agencies.
    A.6.2.3 Carcinogen classification is a one-step, criterion-based process that involves two interrelated determinations: evaluations of strength of evidence and consideration of all other relevant information to place substances with human cancer potential into hazard categories.
    A.6.2.4 Strength of evidence involves the enumeration of tumors in human and animal studies and determination of their level of statistical significance. Sufficient human evidence demonstrates causality between human exposure and the development of cancer, whereas sufficient evidence in animals shows a causal relationship between the agent and an increased incidence of tumors. Limited evidence in humans is demonstrated by a positive association between exposure and cancer, but a causal relationship cannot be stated. Limited evidence in animals is provided when data suggest a carcinogenic effect, but are less than sufficient. (Guidance on consideration of important factors in the classification of carcinogenicity and a more detailed description of the terms "limited" and "sufficient" have been developed by the International Agency for Research on Cancer (IARC) and are provided in non-mandatory Appendix F.)
    A.6.2.5 Weight of evidence: Beyond the determination of the strength of evidence for carcinogenicity, a number of other factors should be considered that influence the overall likelihood that an agent may pose a carcinogenic hazard in humans. The full list of factors that influence this determination is very lengthy, but some of the important ones are considered here.
    A.6.2.5.1 These factors can be viewed as either increasing or decreasing the level of concern for human carcinogenicity. The rela¬tive emphasis accorded to each factor depends upon the amount and coherence of evidence bearing on each. Generally there is a requirement for more complete information to decrease than to increase the level of concern. Additional considerations should be used in evaluating the tumor findings and the other factors in a case-by-case manner.
    A.6.2.5.2 Some important factors which may be taken into consideration, when assessing the overall level of concern are:
    (a) Tumor type and background incidence;

    (b) Multisite responses;

    (c) Progression of lesions to malignancy;

    (d) Reduced tumor latency;

    Additional factors which may increase or decrease the level of concern include:

    (e) Whether responses are in single or both sexes;

    (f) Whether responses are in a single species or several species;

    (g) Structural similarity or not to a substance(s) for which there is good evidence of carcinogenicity;

    (h) Routes of exposure;

    (i) Comparison of absorption, distribution, metabolism and excretion between test animals and humans;

    (j) The possibility of a confounding effect of excessive toxicity at test doses; and,

    (k) Mode of action and its relevance for humans, such as mutagenicity, cytotoxicity with growth stimulation, mitogenesis, immunosuppression.
    Mutagenicity: It is recognized that genetic events are central in the overall process of cancer development. Therefore evidence of mutagenic activity in vivo may indicate that a substance has a potential for carcinogenic effects.
    A.6.2.5.3 A substance that has not been tested for carcinogenicity may in certain instances be classified in Category 1A, Category 1B, or Category 2 based on tumor data from a structural analogue together with substantial support from consi¬deration of other important factors such as formation of common significant metabolites, e.g., for benzidine congener dyes.
    A.6.2.5.4 The classification should also take into consideration whether or not the substance is absorbed by a given route(s); or whether there are only local tumors at the site of administration for the tested route(s), and adequate testing by other major route(s) show lack of carcinogenicity.
    A.6.2.5.5 It is important that whatever is known of the physico-chemical, toxicokinetic and toxicodynamic properties of the substances, as well as any available relevant information on chemical analogues, i.e., structure activity relationship, is taken into consideration when undertaking classification.
    A.6.3 Classification criteria for mixtures
    A.6.3.1 The mixture shall be classified as a carcinogen when at least one ingredient has been classified as a Category 1 or Category 2 carcinogen and is present at or above the appropriate cut-off value/concentration limit as shown in Table A.6.1.
    Table A.6.1: Cut-off values/concentration limits of ingredients of a mixture classified as
    carcinogen that would trigger classification of the mixture
    Ingredient classified as:Category 1 carcinogenCategory 2 carcinogen
    Category 1 carcinogen≥ 0.1 % 
    Category 2 carcinogen ≥ 0.1% (note 1)
    Note: If a Category 2 carcinogen ingredient is present in the mixture at a concentration between 0.1% and 1%, information is required on the SDS for a product. However, a label warning is optional. If a Category 2 carcinogen ingredient is present in the mixture at a concentration of ≥ 1%, both an SDS and a label is required and the information must be included on each.
    A.6.3.2 Classification of mixtures when data are available for the complete mixture
    A mixture may be classified based on the available test data for the mixture as a whole. In such cases, the test results for the mixture as a whole must be shown to be conclusive taking into account dose and other factors such as duration, observations and analysis (e.g., statistical analysis, test sensitivity) of carcinogenicity test systems.
    A.6.3.3 Classification of mixtures when data are not available for the complete mixture: bridging principles
    Where the mixture itself has not been tested to determine its carcinogenic hazard, but there are sufficient data on both the individual ingredients and similar tested mixtures to adequately characterize the hazards of the mixture, these data will be used in accordance with the following bridging principles as found in paragraph A.0.5 of this Appendix: Dilution; Batching; and Substantially similar mixtures.
    A.6.4 Classification of carcinogenicity
    A.6.4.1 Chemical manufacturers, importers and employers evaluating chemicals may treat the following sources as establishing that a substance is a carcinogen or potential carcinogen for hazard communication purposes in lieu of applying the criteria described herein:
    A.6.4.1.1 National Toxicology Program (NTP), "Report on Carcinogens" (latest edition);
    A.6.4.1.2 International Agency for Research on Cancer (IARC) "Monographs on the Evaluation of Carcinogenic Risks to Humans" (latest editions)
    A.6.4.2 Where OSHA has included cancer as a health hazard to be considered by classifiers for a chemical covered by 29 CFR part 1910, Subpart Z, Toxic and Hazardous Substances, chemical manufacturers, importers, and employers shall classify the chemical as a carcinogen.


    A.7 REPRODUCTIVE TOXICITY
    A.7.1 Definitions and general considerations
    A.7.1.1 Reproductive toxicity includes adverse effects on sexual function and fertility in adult males and females, as well as adverse effects on development of the offspring. Some reproductive toxic effects cannot be clearly assigned to either impairment of sexual function and fertility or to developmental toxicity. Nonetheless, chemicals with these effects shall be classified as reproductive toxicants.
    For classification purposes, the known induction of genetically based inheritable effects in the offspring is addressed in Germ cell mutagenicity (See A.5).
    A.7.1.2 Adverse effects on sexual function and fertility means any effect of chemicals that interferes with reproductive ability or sexual capacity. This includes, but is not limited to, alterations to the female and male reproductive system, adverse effects on onset of puberty, gamete production and transport, reproductive cycle normality, sexual behaviour, fertility, parturition, pregnancy outcomes, premature reproductive senescence, or modifications in other functions that are dependent on the integrity of the reproductive systems.
    A.7.1.3 Adverse effects on development of the offspring means any effect of chemicals which interferes with normal development of the conceptus either before or after birth, which is induced during pregnancy or results from parental exposure. These effects can be manifested at any point in the life span of the organism. The major manifestations of developmental toxicity include death of the developing organism, structural abnormality, altered growth and functional deficiency.
    A.7.1.4 Adverse effects on or via lactation are also included in reproductive toxicity, but for classification purposes, such effects are treated separately (See A.7.2.1).
    A.7.2 Classification criteria for substances
    A.7.2.1 For the purpose of classification for reproductive toxicity, substances shall be classified in one of two categories in accordance with Figure A.7.1(a). Effects on sexual function and fertility, and on development, shall be considered. In addition, effects on or via lactation shall be classified in a separate hazard category in accordance with Figure A.7.1(b).
    Figure A.7.1(a): Hazard categories for reproductive toxicants
    CATEGORY 1:






    Category 1A:


    Category 1B:






    CATEGORY 2:
    Known or presumed human reproductive toxicant
    Substance shall be classified in Category 1 for reproductive toxicity when they are known to have produced an adverse effect on sexual function and fertility or on development in humans or when there is evidence from animal studies, possibly supplemented with other information, to provide a strong presumption that the substance has the capacity to interfere with reproduction in humans. The classification of a substance is further distinguished on the basis of whether the evidence for classification is primarily from human data (Category 1A) or from animal data (Category 1B).

    Known human reproductive toxicant
    The classification of a substance in this category is largely based on evidence from humans.

    Presumed human reproductive toxicant
    The classification of a substance in this category is largely based on evidence from experimental animals. Data from animal studies shall provide sufficient evidence of an adverse effect on sexual function and fertility or on development in the absence of other toxic effects, or if occurring together with other toxic effects the adverse effect on reproduction is considered not to be a secondary non-specific consequence of other toxic effects. However, when there is mechanistic information that raises doubt about the relevance of the effect for humans, classification in Category 2 may be more appropriate.

    Suspected human reproductive toxicant
    Substances shall be classified in Category 2 for reproductive toxicity when there is some evidence from humans or experimental animals, possibly supplemented with other information, of an adverse effect on sexual function and fertility, or on development, in the absence of other toxic effects, or if occurring together with other toxic effects the adverse effect on reproduction is considered not to be a secondary non-specific consequence of the other toxic effects, and where the evidence is not sufficiently convincing to place the substance in Category 1. For instance, deficiencies in the study may make the quality of evidence less convincing, and in view of this, Category 2 would be the more appropriate classification.
    Figure A.7.1(b): Hazard category for effects on or via lactation
    EFFECTS ON OR VIA LACTATION

    Effects on or via lactation shall be classified in a separate single category. Chemicals that are absorbed by women and have been shown to interfere with lactation or that may be present (including metabolites) in breast milk in amounts sufficient to cause concern for the health of a breastfed child, shall be classified to indicate this property hazardous to breastfed babies. This classification shall be assigned on the basis of:
    (a) absorption, metabolism, distribution and excretion studies that indicate the likelihood the substance would be present in potentially toxic levels in breast milk; and/or

    (b) results of one or two generation studies in animals which provide clear evidence of adverse effect in the offspring due to transfer in the milk or adverse effect on the quality of the milk; and/or

    (c) human evidence indicating a hazard to babies during the lactation period.
    A.7.2.2 Basis of classification
    A.7.2.2.1 Classification is made on the basis of the criteria, outlined above, an assessment of the total weight of evidence, and the use of expert judgment. Classification as a reproductive toxicant is intended to be used for substances which have an intrinsic, specific property to produce an adverse effect on reproduction and substances should not be so classified if such an effect is produced solely as a non-specific secondary consequence of other toxic effects.
    A.7.2.2.2 In the evaluation of toxic effects on the developing offspring, it is important to consider the possible influence of maternal toxicity.
    A.7.2.2.3 For human evidence to provide the primary basis for a Category 1A classification there must be reliable evidence of an adverse effect on reproduction in humans. Evidence used for classification shall be from well conducted epidemiological studies, if available, which include the use of appropriate controls, balanced assessment, and due consideration of bias or confounding factors. Less rigorous data from studies in humans may be sufficient for a Category 1A classification if supplemented with adequate data from studies in experimental animals, but classification in Category 1B may also be considered.
    A.7.2.3 Weight of evidence
    A.7.2.3.1 Classification as a reproductive toxicant is made on the basis of an assessment of the total weight of evidence using expert judgment. This means that all available information that bears on the determination of reproductive toxicity is considered together. Included is information such as epidemiological studies and case reports in humans and specific reproduction studies along with sub-chronic, chronic and special study results in animals that provide relevant information regarding toxicity to reproductive and related endocrine organs. Evaluation of substances chemically related to the material under study may also be included, particularly when information on the material is scarce. The weight given to the available evidence will be influenced by factors such as the quality of the studies, consistency of results, nature and severity of effects, level of statistical significance for intergroup differences, number of endpoints affected, relevance of route of administration to humans and freedom from bias. Both positive and negative results are considered together in a weight of evidence determination. However, a single, positive study performed according to good scientific principles and with statistically or biologically significant positive results may justify classification (See also A.7.2.2.3).
    A.7.2.3.2 Toxicokinetic studies in animals and humans, site of action and mechanism or mode of action study results may provide relevant information, which could reduce or increase concerns about the hazard to human health. If it is conclusively demonstrated that the clearly identified mechanism or mode of action has no relevance for humans or when the toxicokinetic differences are so marked that it is certain that the hazardous property will not be expressed in humans then a chemical which produces an adverse effect on reproduction in experimental animals should not be classified.
    A.7.2.3.3 In some reproductive toxicity studies in experimental animals the only effects recorded may be considered of low or minimal toxicological significance and classification may not necessarily be the outcome. These effects include, for example, small changes in semen parameters or in the incidence of spontaneous defects in the fetus, small changes in the proportions of common fetal variants such as are observed in skeletal examinations, or in fetal weights, or small differences in postnatal developmental assessments.
    A.7.2.3.4 Data from animal studies shall provide sufficient evidence of specific reproductive toxicity in the absence of other systemic toxic effects. However, if developmental toxicity occurs together with other toxic effects in the dam (mother), the potential influence of the generalized adverse effects should be assessed to the extent possible. The preferred approach is to consider adverse effects in the embryo/fetus first, and then evaluate maternal toxicity, along with any other factors which are likely to have influenced these effects, as part of the weight of evidence. In general, developmental effects that are observed at maternally toxic doses should not be automatically discounted. Discounting developmental effects that are observed at maternally toxic doses can only be done on a case-by-case basis when a causal relationship is established or refuted.
    A.7.2.3.5 If appropriate information is available it is important to try to determine whether developmental toxicity is due to a specific maternally mediated mechanism or to a non-specific secondary mechanism, like maternal stress and the disruption of homeostasis. Generally, the presence of maternal toxicity should not be used to negate findings of embryo/fetal effects, unless it can be clearly demonstrated that the effects are secondary non-specific effects. This is especially the case when the effects in the offspring are significant, e.g., irreversible effects such as structural malformations. In some situations it is reasonable to assume that reproductive toxicity is due to a secondary consequence of maternal toxicity and discount the effects, for example if the chemical is so toxic that dams fail to thrive and there is severe inanition; they are incapable of nursing pups; or they are prostrate or dying.
    A.7.2.4 Maternal toxicity
    A.7.2.4.1 Development of the offspring throughout gestation and during the early postnatal stages can be influenced by toxic effects in the mother either through non-specific mechanisms related to stress and the disruption of maternal homeostasis, or by specific maternally-mediated mechanisms. So, in the interpretation of the developmental outcome to decide classification for developmental effects it is important to consider the possible influence of maternal toxicity. This is a complex issue because of uncertainties surrounding the relationship between maternal toxicity and developmental outcome. Expert judgment and a weight of evidence approach, using all available studies, shall be used to determine the degree of influence to be attributed to maternal toxicity when interpreting the criteria for classification for developmental effects. The adverse effects in the embryo/fetus shall be first considered, and then maternal toxicity, along with any other factors which are likely to have influenced these effects, as weight of evidence, to help reach a conclusion about classification.
    A.7.2.4.2 Based on pragmatic observation, it is believed that maternal toxicity may, depending on severity, influence development via non-specific secondary mechanisms, producing effects such as depressed fetal weight, retarded ossification, and possibly resorptions and certain malformations in some strains of certain species. However, the limited numbers of studies which have investigated the relationship between developmental effects and general maternal toxicity have failed to demonstrate a consistent, reproducible relationship across species. Developmental effects which occur even in the presence of maternal toxicity are considered to be evidence of developmental toxicity, unless it can be unequivocally demonstrated on a case by case basis that the developmental effects are secondary to maternal toxicity. Moreover, classification shall be considered where there is a significant toxic effect in the offspring, e.g., irreversible effects such as structural malformations, embryo/fetal lethality, or significant post-natal functional deficiencies.
    A.7.2.4.3 Classification shall not automatically be discounted for chemicals that produce developmental toxicity only in association with maternal toxicity, even if a specific maternally-mediated mechanism has been demonstrated. In such a case, classification in Category 2 may be considered more appropriate than Category 1. However, when a chemical is so toxic that maternal death or severe inanition results, or the dams (mothers) are prostrate and incapable of nursing the pups, it is reasonable to assume that developmental toxicity is produced solely as a secondary consequence of maternal toxicity and discount the developmental effects. Classification is not necessarily the outcome in the case of minor developmental changes, e.g., a small reduction in fetal/pup body weight or retardation of ossification when seen in association with maternal toxicity.
    A.7.2.4.4 Some of the endpoints used to assess maternal toxicity are provided below. Data on these endpoints, if available, shall be evaluated in light of their statistical or biological significance and dose-response relationship.
    (a) Maternal mortality: An increased incidence of mortality among the treated dams over the controls shall be considered evidence of maternal toxicity if the increase occurs in a dose-related manner and can be attributed to the systemic toxicity of the test material. Maternal mortality greater than 10% is considered excessive and the data for that dose level shall not normally be considered to need further evaluation.

    (b) Mating index (Number of animals with seminal plugs or sperm/Number of mated x 100)

    (c) Fertility index (Number of animals with implants/Number of matings x 100)

    (d) Gestation length (If allowed to deliver)

    (e) Body weight and body weight change: Consideration of the maternal body weight change and/or adjusted (corrected) maternal body weight shall be included in the evaluation of maternal toxicity whenever such data are available. The calculation of an adjusted (corrected) mean maternal body weight change, which is the difference between the initial and terminal body weight minus the gravid uterine weight (or alternatively, the sum of the weights of the fetuses), may indicate whether the effect is maternal or intrauterine. In rabbits, the body weight gain may not be a useful indicator of maternal toxicity because of normal fluctuations in body weight during pregnancy.

    (f) Food and water consumption (if relevant): The observation of a significant decrease in the average food or water consumption in treated dams (mothers) compared to the control group may be useful in evaluating maternal toxicity, particularly when the test material is administered in the diet or drinking water. Changes in food or water consumption must be evaluated in conjunction with maternal body weights when determining if the effects noted are reflective of maternal toxicity or more simply, unpalatability of the test material in feed or water.

    (g) Clinical evaluations (including clinical signs, markers, and hematology and clinical chemistry studies): The observation of increased incidence of significant clinical signs of toxicity in treated dams (mothers) relative to the control group is useful in evaluating maternal toxicity. If this is to be used as the basis for the assessment of maternal toxicity, the types, incidence, degree and duration of clinical signs shall be reported in the study. Clinical signs of maternal intoxication include, but are not limited to: coma, prostration, hyperactivity, loss of righting reflex, ataxia, or labored breathing.

    (h) Post-mortem data: Increased incidence and/or severity of post-mortem findings may be indicative of maternal toxicity. This can include gross or microscopic pathological findings or organ weight data, including absolute organ weight, organ to body weight ratio, or organ to brain weight ratio. When supported by findings of adverse histopathological effects in the affected organ(s), the observation of a significant change in the average weight of suspected target organ(s) of treated dams (mothers), compared to those in the control group, may be considered evidence of maternal toxicity.
    A.7.2.5 Animal and experimental data
    A.7.2.5.1 A number of scientifically validated test methods are available, including methods for developmental toxicity testing (e.g., OECD Test Guideline 414, ICH Guideline S5A, 1993), methods for peri- and post-natal toxicity testing (e.g., ICH S5B, 1995), and methods for one or two-generation toxicity testing (e.g., OECD Test Guidelines 415, 416)
    A.7.2.5.2 Results obtained from screening tests (e.g., OECD Guidelines 421 - Reproduction/ Developmental Toxicity Screening Test, and 422 - Combined Repeated Dose Toxicity Study with Reproduction/Development Toxicity Screening Test) can also be used to justify classification, although the quality of this evidence is less reliable than that obtained through full studies.
    A.7.2.5.3 Adverse effects or changes, seen in short- or long-term repeated dose toxicity studies, which are judged likely to impair reproductive function and which occur in the absence of significant generalized toxicity, may be used as a basis for classification, e.g., histopathological changes in the gonads.
    A.7.2.5.4 Evidence from in vitro assays, or non-mammalian tests, and from analogous substances using structure-activity relationship (SAR), can contribute to the procedure for classification. In all cases of this nature, expert judgment must be used to assess the adequacy of the data. Inadequate data shall not be used as a primary support for classification.
    A.7.2.5.5 It is preferable that animal studies are conducted using appropriate routes of administration which relate to the potential route of human exposure. However, in practice, reproductive toxicity studies are commonly conducted using the oral route, and such studies will normally be suitable for evaluating the hazardous properties of the substance with respect to reproductive toxicity. However, if it can be conclusively demonstrated that the clearly identified mechanism or mode of action has no relevance for humans or when the toxicokinetic differences are so marked that it is certain that the hazardous property will not be expressed in humans then a substance which produces an adverse effect on reproduction in experimental animals should not be classified.
    A.7.2.5.6 Studies involving routes of administration such as intravenous or intraperitoneal injection, which may result in exposure of the reproductive organs to unrealistically high levels of the test substance, or elicit local damage to the reproductive organs, e.g., by irritation, must be interpreted with extreme caution and on their own are not normally the basis for classification.
    A.7.2.5.7 There is general agreement about the concept of a limit dose, above which the production of an adverse effect may be considered to be outside the criteria which lead to classification. Some test guidelines specify a limit dose, other test guidelines qualify the limit dose with a statement that higher doses may be necessary if anticipated human exposure is sufficiently high that an adequate margin of exposure would not be achieved. Also, due to species differences in toxicokinetics, establishing a specific limit dose may not be adequate for situations where humans are more sensitive than the animal model.
    A.7.2.5.8 In principle, adverse effects on reproduction seen only at very high dose levels in animal studies (for example doses that induce prostration, severe inappetence, excessive mortality) do not normally lead to classification, unless other information is available, for example, toxicokinetics information indicating that humans may be more susceptible than animals, to suggest that classification is appropriate.
    A.7.2.5.9 However, specification of the actual "limit dose" will depend upon the test method that has been employed to provide the test results.
    A.7.3 Classification criteria for mixtures
    A.7.3.1 Classification of mixtures when data are available for all ingredients or only for some ingredients of the mixture
    A.7.3.1.1 The mixture shall be classified as a reproductive toxicant when at least one ingredient has been classified as a Category 1 or Category 2 reproductive toxicant and is present at or above the appropriate cut-off value/concentration limit specified in Table A.7.1 for Category 1 and 2, respectively.
    A.7.3.1.2 The mixture shall be classified for effects on or via lactation when at least one ingredient has been classified for effects on or via lactation and is present at or above the appropriate cut-off value/concentration limit specified in Table A.7.1 for the additional category for effects on or via lactation.
    Table A.7.1: Cut-off values/concentration limits of ingredients of a mixture classified as
    reproductive toxicants or for effects on or via lactation that trigger classification of the mixture




    Ingredients classified as:
    Cut-off values/concentration limits triggering classification of a mixture as:

    Category 1
    reproductive toxicant

    Category 2
    reproductive toxicant
    Additional category
    for effects on or via
    lactation
    Category 1
    reproductive toxicant
    ≥ 0.1%  
    Category 2
    reproductive toxicant
     ≥ 0.1% 
    Additional category for effects
    on or via lactation
      ≥ 0.1%
    A.7.3.2 Classification of mixtures when data are available for the complete mixture
    Available test data for the mixture as a whole may be used for classification on a case-by-case basis. In such cases, the test results for the mixture as a whole must be shown to be conclusive taking into account dose and other factors such as duration, observations and analysis (e.g., statistical analysis, test sensitivity) of reproduction test systems.
    A.7.3.3 Classification of mixtures when data are not available for the complete mixture: bridging principles
    A.7.3.3.1 Where the mixture itself has not been tested to determine its reproductive toxicity, but there are sufficient data on both the individual ingredients and similar tested mixtures to adequately characterize the hazards of the mixture, these data shall be used in accordance with the following bridging principles as found in paragraph A.0.5 of this Appendix: Dilution, Batching, and Substantially similar mixtures.


    A.8 SPECIFIC TARGET ORGAN TOXICITY
    SINGLE EXPOSURE
    A.8.1 Definitions and general considerations
    A.8.1.1 Specific target organ toxicity - single exposure, (STOT-SE) means specific, non-lethal target organ toxicity arising from a single exposure to a chemical. All significant health effects that can impair function, both reversible and irreversible, immediate and/or delayed and not specifically addressed in A.1 to A.7 and A.10 of this Appendix are included. Specific target organ toxicity following repeated exposure is classified in accordance with SPECIFIC TARGET ORGAN TOXICITY – REPEATED EXPOSURE (A.9 of this Appendix) and is therefore not included here.
    A.8.1.2 Classification identifies the chemical as being a specific target organ toxicant and, as such, it presents a potential for adverse health effects in people who are exposed to it.
    A.8.1.3 The adverse health effects produced by a single exposure include consistent and identifiable toxic effects in humans; or, in experimental animals, toxicologically significant changes which have affected the function or morphology of a tissue/organ, or have produced serious changes to the biochemistry or hematology of the organism, and these changes are relevant for human health. Human data is the primary source of evidence for this hazard class.
    A.8.1.4 Assessment shall take into consideration not only significant changes in a single organ or biological system but also generalized changes of a less severe nature involving several organs.
    A.8.1.5 Specific target organ toxicity can occur by any route that is relevant for humans, i.e., principally oral, dermal or inhalation.
    A.8.1.6 The classification criteria for specific organ systemic toxicity single exposure are organized as criteria for substances Categories 1 and 2 (See A.8.2.1), criteria for substances Category 3 (See A.8.2.2) and criteria for mixtures (See A.8.3). See also Figure A.8.1.
    A.8.2 Classification criteria for substances
    A.8.2.1 Substances of Category 1 and Category 2
    A.8.2.1.1 Substances shall be classified for immediate or delayed effects separately, by the use of expert judgment on the basis of the weight of all evidence available, including the use of recommended guidance values (See A.8.2.1.9). Substances shall then be classified in Category 1 or 2, depending upon the nature and severity of the effect(s) observed, in accordance with Figure A.8.1.
    Figure A.8.1: Hazard categories for specific target organ toxicity following single exposure
    CATEGORY 1:








    CATEGORY 2:






    CATEGORY 3:
    Substances that have produced significant toxicity in humans, or that, on the basis of evidence from studies in experimental animals can be presumed to have the potential to produce significant toxicity in humans following single exposure
    Substances are classified in Category 1 for STOT-SE on the basis of:
    (a) reliable and good quality evidence from human cases or epidemiological studies; or
    (b) observations from appropriate studies in experimental animals in which significant and/or severe toxic effects of relevance to human health were produced at generally low exposure concentrations. Guidance dose/concentration values are provided below (See A.8.2.1.9) to be used as part of weight-of-evidence evaluation.

    Substances that, on the basis of evidence from studies in experimental animals, can be presumed to have the potential to be harmful to human health following single exposure
    Substances are classified in Category 2 for STOT-SE on the basis of observations from appropriate studies in experimental animals in which significant toxic effects, of relevance to human health, were produced at generally moderate exposure concentrations. Guidance dose/concentration values are provided below (See A.8.2.1.9) in order to help in classification.
    In exceptional cases, human evidence can also be used to place a substance in Category 2 (See A.8.2.1.6).

    Transient target organ effects
    There are target organ effects for which a substance does not meet the criteria to be classified in Categories 1 or 2 indicated above. These are effects which adversely alter human function for a short duration after exposure and from which humans may recover in a reasonable period without leaving significant alteration of structure or function. This category only includes narcotic effects and respiratory tract irritation. Substances are classified specifically for these effects as discussed in A.8.2.2.
    Note: The primary target organ/system shall be identified where possible, and where this is not possible, the substance shall be identified as a general toxicant. The data shall be evaluated and, where possible, shall not include secondary effects (e.g., a hepatotoxicant can produce secondary effects in the nervous or gastro-intestinal systems).
    A.8.2.1.2 The relevant route(s) of exposure by which the classified substance produces damage shall be identified.
    A.8.2.1.3 Classification is determined by expert judgment, on the basis of the weight of all evidence available including the guidance presented below.
    A.8.2.1.4 Weight of evidence of all available data, including human incidents, epidemiology, and studies conducted in experimental animals is used to substantiate specific target organ toxic effects that merit classification.
    A.8.2.1.5 The information required to evaluate specific target organ toxicity comes either from single exposure in humans (e.g., exposure at home, in the workplace or environmentally), or from studies conducted in experimental animals. The standard animal studies in rats or mice that provide this information are acute toxicity studies which can include clinical observations and detailed macroscopic and microscopic examination to enable the toxic effects on target tissues/organs to be identified. Results of acute toxicity studies conducted in other species may also provide relevant information.
    A.8.2.1.6 In exceptional cases, based on expert judgment, it may be appropriate to place certain substances with human evidence of target organ toxicity in Category 2: (a) when the weight of human evidence is not sufficiently convincing to warrant Category 1 classification, and/or (b) based on the nature and severity of effects. Dose/concentration levels in humans shall not be considered in the classification and any available evidence from animal studies shall be consistent with the Category 2 classification. In other words, if there are also animal data available on the substance that warrant Category 1 classification, the chemical shall be classified as Category 1.
    A.8.2.1.7 Effects considered to support classification for Category 1 and 2
    A.8.2.1.7.1 Classification is supported by evidence associating single exposure to the substance with a consistent and identifiable toxic effect.
    A.8.2.1.7.2 Evidence from human experience/incidents is usually restricted to reports of adverse health consequences, often with uncertainty about exposure conditions, and may not provide the scientific detail that can be obtained from well-conducted studies in experimental animals.
    A.8.2.1.7.3 Evidence from appropriate studies in experimental animals can furnish much more detail, in the form of clinical observations, and macroscopic and microscopic pathological examination and this can often reveal hazards that may not be life-threatening but could indicate functional impairment. Consequently all available evidence, and evidence relevance to human health, must be taken into consideration in the classification process. Relevant toxic effects in humans and/or animals include, but are not limited to:
    (a) Morbidity resulting from single exposure;

    (b) Significant functional changes, more than transient in nature, in the respiratory system, central or peripheral nervous systems, other organs or other organ systems, including signs of central nervous system depression and effects on special senses (e.g., sight, hearing and sense of smell);

    (c) Any consistent and significant adverse change in clinical biochemistry, hematology, or urinalysis parameters;

    (d) Significant organ damage that may be noted at necropsy and/or subsequently seen or confirmed at microscopic examination;

    (e) Multi-focal or diffuse necrosis, fibrosis or granuloma formation in vital organs with regenerative capacity;

    (f) Morphological changes that are potentially reversible but provide clear evidence of marked organ dysfunction; and,

    (g) Evidence of appreciable cell death (including cell degeneration and reduced cell number) in vital organs incapable of regeneration.
    A.8.2.1.8 Effects considered not to support classification for Category 1 and 2
    Effects may be seen in humans and/or animals that do not justify classification. Such effects include, but are not limited to:
    (a) Clinical observations or small changes in bodyweight gain, food consumption or water intake that may have some toxicological importance but that do not, by themselves, indicate "significant" toxicity;

    (b) Small changes in clinical biochemistry, hematology or urinalysis parameters and/or transient effects, when such changes or effects are of doubtful or of minimal toxicological importance;

    (c) Changes in organ weights with no evidence of organ dysfunction;

    (d) Adaptive responses that are not considered toxicologically relevant; and,

    (e) Substance-induced species-specific mechanisms of toxicity, i.e., demonstrated with reasonable certainty to be not relevant for human health, shall not justify classification.
    A.8.2.1.9 Guidance values to assist with classification based on the results obtained from studies conducted in experimental animals for Category 1 and 2
    A.8.2.1.9.1 In order to help reach a decision about whether a substance shall be classified or not, and to what degree it shall be classified (Category 1 vs. Category 2), dose/concentration "guidance values" are provided for consideration of the dose/concentration which has been shown to produce significant health effects. The principal argument for proposing such guidance values is that all chemicals are potentially toxic and there has to be a reasonable dose/concentration above which a degree of toxic effect is acknowledged.
    A.8.2.1.9.2 Thus, in animal studies, when significant toxic effects are observed that indicate classification, consideration of the dose/concentration at which these effects were seen, in relation to the suggested guidance values, provides useful information to help assess the need to classify (since the toxic effects are a consequence of the hazardous property(ies) and also the dose/concentration).
    A.8.2.1.9.3 The guidance value (C) ranges for single-dose exposure which has produced a significant non-lethal toxic effect are those applicable to acute toxicity testing, as indicated in Table A.8.1.
    Table A.8.1: Guidance value ranges for single-dose exposures
     Guidance value ranges for:
    Route of exposureUnitsCategory 1Category 2Category 3
    Oral (rat)mg/kg body weightC ≤ 3002000 ≥ C > 300

    Guidance
    values do not
    apply
    Dermal (rat or rabbit)mg/kg body weightC ≤ 10002000 ≥ C > 1000
    Inhalation (rat) gasppmV/4hC ≤ 250020,000 ≥ C > 2500
    Inhalation (rat) vapormg/1/4hC ≤ 1020 ≥ C > 10
    Inhalation (rat) dust/mist/fumemg/l/4hC ≤ 1.05.0 ≥ C > 1.0
    A.8.2.1.9.4 The guidance values and ranges mentioned in Table A.8.1 are intended only for guidance purposes, i.e., to be used as part of the weight of evidence approach, and to assist with decisions about classification. They are not intended as strict demarcation values. Guidance values are not provided for Category 3 since this classification is primarily based on human data; animal data may be included in the weight of evidence evaluation.
    A.8.2.1.9.5 Thus, it is feasible that a specific profile of toxicity occurs at a dose/concentration below the guidance value, e.g., < 2000 mg/kg body weight by the oral route, however the nature of the effect may result in the decision not to classify. Conversely, a specific profile of toxicity may be seen in animal studies occurring at above a guidance value, e.g., ≥ 2000 mg/kg body weight by the oral route, and in addition there is supplementary information from other sources, e.g., other single dose studies, or human case experience, which supports a conclusion that, in view of the weight of evidence, classification is the prudent action to take.
    A.8.2.1.10 Other considerations
    A.8.2.1.10.1 When a substance is characterized only by use of animal data the classification process includes reference to dose/concentration guidance values as one of the elements that contribute to the weight of evidence approach.
    A.8.2.1.10.2 When well-substantiated human data are available showing a specific target organ toxic effect that can be reliably attributed to single exposure to a substance, the substance shall be classified. Positive human data, regardless of probable dose, predominates over animal data. Thus, if a substance is unclassified because specific target organ toxicity observed was considered not relevant or significant to humans, if subsequent human incident data become available showing a specific target organ toxic effect, the substance shall be classified.
    A.8.2.1.10.3 A substance that has not been tested for specific target organ toxicity shall, where appropriate, be classified on the basis of data from a scientifically validated structure activity relationship and expert judgment-based extrapolation from a structural analogue that has previously been classified together with substantial support from consideration of other important factors such as formation of common significant metabolites.
    A.8.2.2 Substances of Category 3
    A.8.2.2.1 Criteria for respiratory tract irritation
    The criteria for classifying substances as Category 3 for respiratory tract irritation are:
    (a) Respiratory irritant effects (characterized by localized redness, edema, pruritis and/or pain) that impair function with symptoms such as cough, pain, choking, and breathing difficulties are included. It is recognized that this evaluation is based primarily on human data;

    (b) Subjective human observations supported by objective measurements of clear respiratory tract irritation (RTI) (e.g., electrophysiological responses, biomarkers of inflammation in nasal or bronchoalveolar lavage fluids);

    (c) The symptoms observed in humans shall also be typical of those that would be produced in the exposed population rather than being an isolated idiosyncratic reaction or response triggered only in individuals with hypersensitive airways. Ambiguous reports simply of "irritation" should be excluded as this term is commonly used to describe a wide range of sensations including those such as smell, unpleasant taste, a tickling sensation, and dryness, which are outside the scope of classification for respiratory tract irritation;

    (d) There are currently no scientifically validated animal tests that deal specifically with RTI; however, useful information may be obtained from the single and repeated inhalation toxicity tests. For example, animal studies may provide useful information in terms of clinical signs of toxicity (dyspnoea, rhinitis etc) and histopathology (e.g., hyperemia, edema, minimal inflammation, thickened mucous layer) which are reversible and may be reflective of the characteristic clinical symptoms described above. Such animal studies can be used as part of weight of evidence evaluation; and,

    (e) This special classification will occur only when more severe organ effects including the respiratory system are not observed as those effects would require a higher classification.
    A.8.2.2.2 Criteria for narcotic effects
    The criteria for classifying substances in Category 3 for narcotic effects are:
    (a) Central nervous system depression including narcotic effects in humans such as drowsiness, narcosis, reduced alertness, loss of reflexes, lack of coordination, and vertigo are included. These effects can also be manifested as severe headache or nausea, and can lead to reduced judgment, dizziness, irritability, fatigue, impaired memory function, deficits in perception and coordination, reaction time, or sleepiness; and,

    (b) Narcotic effects observed in animal studies may include lethargy, lack of coordination righting reflex, narcosis, and ataxia. If these effects are not transient in nature, then they shall be considered for classification as Category 1 or 2.
    A.8.3 Classification criteria for mixtures
    A.8.3.1 Mixtures are classified using the same criteria as for substances, or alternatively as described below. As with substances, mixtures may be classified for specific target organ toxicity following single exposure, repeated exposure, or both.
    A.8.3.2 Classification of mixtures when data are available for the complete mixture
    When reliable and good quality evidence from human experience or appropriate studies in experimental animals, as described in the criteria for substances, is available for the mixture, then the mixture shall be classified by weight of evidence evaluation of this data. Care shall be exercised in evaluating data on mixtures, that the dose, duration, observation or analysis, do not render the results inconclusive.
    A.8.3.3 Classification of mixtures when data are not available for the complete mixture: bridging principles
    A.8.3.3.1 Where the mixture itself has not been tested to determine its specific target organ toxicity, but there are sufficient data on both the individual ingredients and similar tested mixtures to adequately characterize the hazards of the mixture, these data shall be used in accordance with the following bridging principles as found in paragraph A.0.5 of this Appendix: Dilution, Batching, Concentration of mixtures, Interpolation within one toxicity category, Substantially similar mixtures, or Aerosols.
    A.8.3.4 Classification of mixtures when data are available for all ingredients or only for some ingredients of the mixture
    A.8.3.4.1 Where there is no reliable evidence or test data for the specific mixture itself, and the bridging principles cannot be used to enable classification, then classification of the mixture is based on the classification of the ingredient substances. In this case, the mixture shall be classified as a specific target organ toxicant (specific organ specified), following single exposure, repeated exposure, or both when at least one ingredient has been classified as a Category 1 or Category 2 specific target organ toxicant and is present at or above the appropriate cut-off value/concentration limit specified in Table A.8.2 for Categories 1 and 2, respectively.
    Table A.8.2: Cut-off values/concentration limits of ingredients of a mixture classified as a
    specific target organ toxicant that would trigger classification of the mixture as Category 1 or 2



    Ingredients classified as:
    Cut-off values/concentration limits triggering classification of a
    mixture as:
    Category 1Category 2
    Category 1
    Target organ toxicant

    ≥ 1.0 %
     
    Category 2
    Target organ toxicant
     
    ≥ 1.0 %
    A.8.3.4.2 These cut-off values and consequent classifications shall be applied equally and appropriately to both single- and repeated-dose target organ toxicants.
    A.8.3.4.3 Mixtures shall be classified for either or both single and repeated dose toxicity independently.
    A.8.3.4.4 Care shall be exercised when toxicants affecting more than one organ system are combined that the potentiation or synergistic interactions are considered, because certain substances can cause target organ toxicity at < 1% concentration when other ingredients in the mixture are known to potentiate its toxic effect.
    A.8.3.4.5 Care shall be exercised when extrapolating the toxicity of a mixture that contains Category 3 ingredient(s). A cut-off value/concentration limit of 20%, considered as an additive of all Category 3 ingredients for each hazard endpoint, is appropriate; however, this cut-off value/concentration limit may be higher or lower depending on the Category 3 ingredient(s) involved and the fact that some effects such as respiratory tract irritation may not occur below a certain concentration while other effects such as narcotic effects may occur below this 20% value. Expert judgment shall be exercised. Respiratory tract irritation and narcotic effects are to be evaluated separately in accordance with the criteria given in A.8.2.2. When conducting classifications for these hazards, the contribution of each ingredient should be considered additive, unless there is evidence that the effects are not additive.


    A.9 SPECIFIC TARGET ORGAN TOXICITY
    REPEATED OR PROLONGED EXPOSURE
    A.9.1 Definitions and general considerations
    A.9.1.1 Specific target organ toxicity - repeated exposure (STOT-RE) means specific target organ toxicity arising from repeated exposure to a substance or mixture. All significant health effects that can impair function, both reversible and irreversible, immediate and/or delayed and not specifically addressed in A.1 to A.7 and A.10 of this Appendix are included. Specific target organ toxicity following a single-event exposure is classified in accordance with SPECIFIC TARGET ORGAN TOXICITY – SINGLE EXPOSURE (A.8 of this Appendix) and is therefore not included here.
    A.9.1.2 Classification identifies the substance or mixture as being a specific target organ toxicant and, as such, it may present a potential for adverse health effects in people who are exposed to it.
    A.9.1.3 These adverse health effects produced by repeated exposure include consistent and identifiable toxic effects in humans, or, in experimental animals, toxicologically significant changes which have affected the function or morphology of a tissue/organ, or have produced serious changes to the biochemistry or hematology of the organism and these changes are relevant for human health. Human data will be the primary source of evidence for this hazard class.
    A.9.1.4 Assessment shall take into consideration not only significant changes in a single organ or biological system but also generalized changes of a less severe nature involving several organs.
    A.9.1.5 Specific target organ toxicity can occur by any route that is relevant for humans, e.g., principally oral, dermal or inhalation.
    A.9.2 Classification criteria for substances
    A.9.2.1 Substances shall be classified as STOT - RE by expert judgment on the basis of the weight of all evidence available, including the use of recommended guidance values which take into account the duration of exposure and the dose/concentration which produced the effect(s), (See A.9.2.9). Substances shall be placed in one of two categories, depending upon the nature and severity of the effect(s) observed, in accordance with Figure A.9.1.
    Figure A.9.1: Hazard categories for specific target organ toxicity following repeated exposure
    CATEGORY 1:








    CATEGORY 2:
    Substances that have produced significant toxicity in humans, or that, on the basis of evidence from studies in experimental animals can be presumed to have the potential to produce significant toxicity in humans following repeated or prolonged exposure
    Substances are classified in Category 1 for specific target organ toxicity (repeated exposure) on the basis of:
    (a) reliable and good quality evidence from human cases or epidemiological studies; or,
    (b) observations from appropriate studies in experimental animals in which significant and/or severe toxic effects, of relevance to human health, were produced at generally low exposure concentrations. Guidance dose/concentration values are provided below (See A.9.2.9) to be used as part of weight-of-evidence evaluation.

    Substances that, on the basis of evidence from studies in experimental animals can be presumed to have the potential to be harmful to human health following repeated or prolonged exposure
    Substances are classified in Category 2 for specific target organ toxicity (repeated exposure) on the basis of observations from appropriate studies in experimental animals in which significant toxic effects, of relevance to human health, were produced at generally moderate exposure concentrations. Guidance dose/concentration values are provided below (See A.9.2.9) in order to help in classification.
    In exceptional cases human evidence can also be used to place a substance in Category 2 (See A.9.2.6).
    Note: The primary target organ/system shall be identified where possible, or the substance shall be identified as a general toxicant. The data shall be carefully evaluated and, where possible, shall not include secondary effects (e.g., a hepatotoxicant can produce secondary effects in the nervous or gastro-intestinal systems).
    A.9.2.2 The relevant route of exposure by which the classified substance produces damage shall be identified.
    A.9.2.3 Classification is determined by expert judgment, on the basis of the weight of all evidence available including the guidance presented below.
    A.9.2.4 Weight of evidence of all data, including human incidents, epidemiology, and studies conducted in experimental animals, is used to substantiate specific target organ toxic effects that merit classification.
    A.9.2.5 The information required to evaluate specific target organ toxicity comes either from repeated exposure in humans, e.g., exposure at home, in the workplace or environmentally, or from studies conducted in experimental animals. The standard animal studies in rats or mice that provide this information are 28 day, 90 day or lifetime studies (up to 2 years) that include hematological, clinico-chemical and detailed macroscopic and microscopic examination to enable the toxic effects on target tissues/organs to be identified. Data from repeat dose studies performed in other species may also be used. Other long-term exposure studies, e.g., for carcinogenicity, neurotoxicity or reproductive toxicity, may also provide evidence of specific target organ toxicity that could be used in the assessment of classification.
    A.9.2.6 In exceptional cases, based on expert judgment, it may be appropriate to place certain substances with human evidence of specific target organ toxicity in Category 2: (a) when the weight of human evidence is not sufficiently convincing to warrant Category 1 classification, and/or (b) based on the nature and severity of effects. Dose/concentration levels in humans shall not be considered in the classification and any available evidence from animal studies shall be consistent with the Category 2 classification. In other words, if there are also animal data available on the substance that warrant Category 1 classification, the substance shall be classified as Category 1.
    A.9.2.7 Effects considered to support classification
    A.9.2.7.1 Classification is supported by reliable evidence associating repeated exposure to the substance with a consistent and identifiable toxic effect.
    A.9.2.7.2 Evidence from human experience/incidents is usually restricted to reports of adverse health consequences, often with uncertainty about exposure conditions, and may not provide the scientific detail that can be obtained from well-conducted studies in experimental animals.
    A.9.2.7.3 Evidence from appropriate studies in experimental animals can furnish much more detail, in the form of clinical observations, hematology, clinical chemistry, macroscopic and microscopic pathological examination and this can often reveal hazards that may not be life-threatening but could indicate functional impairment. Consequently all available evidence, and relevance to human health, must be taken into consideration in the classification process. Relevant toxic effects in humans and/or animals include, but are not limited to:
    (a) Morbidity or death resulting from repeated or long-term exposure. Morbidity or death may result from repeated exposure, even to relatively low doses/concentrations, due to bioaccumulation of the substance or its metabolites, or due to the overwhelming of the de-toxification process by repeated exposure;

    (b) Significant functional changes in the central or peripheral nervous systems or other organ systems, including signs of central nervous system depression and effects on special senses (e.g., sight, hearing and sense of smell);

    (c) Any consistent and significant adverse change in clinical biochemistry, hematology, or urinalysis parameters;

    (d) Significant organ damage that may be noted at necropsy and/or subsequently seen or confirmed at microscopic examination;

    (e) Multi-focal or diffuse necrosis, fibrosis or granuloma formation in vital organs with regenerative capacity;

    (f) Morphological changes that are potentially reversible but provide clear evidence of marked organ dysfunction (e.g., severe fatty change in the liver); and,

    (g) Evidence of appreciable cell death (including cell degeneration and reduced cell number) in vital organs incapable of regeneration.
    A.9.2.8 Effects considered not to support classification
    Effects may be seen in humans and/or animals that do not justify classification. Such effects include, but are not limited to:
    (a) Clinical observations or small changes in bodyweight gain, food consumption or water intake that may have some toxicological importance but that do not, by themselves, indicate "significant" toxicity;

    (b) Small changes in clinical biochemistry, hematology or urinalysis parameters and /or transient effects, when such changes or effects are of doubtful or of minimal toxicological importance;

    (c) Changes in organ weights with no evidence of organ dysfunction;

    (d) Adaptive responses that are not considered toxicologically relevant;

    (e) Substance-induced   species-specific   mechanisms   of   toxicity,   i.e., demonstrated with reasonable certainty to be not relevant for human health, shall not justify classification.
    A.9.2.9 Guidance values to assist with classification based on the results obtained from studies conducted in experimental animals
    A.9.2.9.1 In studies conducted in experimental animals, reliance on observation of effects alone, without reference to the duration of experimental exposure and dose/concentration, omits a fundamental concept of toxicology, i.e., all substances are potentially toxic, and what determines the toxicity is a function of the dose/concentration and the duration of exposure. In most studies conducted in experimental animals the test guidelines use an upper limit dose value.
    A.9.2.9.2 In order to help reach a decision about whether a substance shall be classified or not, and to what degree it shall be classified (Category 1 vs. Category 2), dose/concentration "guidance values" are provided in Table A.9.1 for consideration of the dose/concentration which has been shown to produce significant health effects. The principal argument for proposing such guidance values is that all chemicals are potentially toxic and there has to be a reasonable dose/concentration above which a degree of toxic effect is acknowledged. Also, repeated-dose studies conducted in experimental animals are designed to produce toxicity at the highest dose used in order to optimize the test objective and so most studies will reveal some toxic effect at least at this highest dose. What is therefore to be decided is not only what effects have been produced, but also at what dose/concentration they were produced and how relevant is that for humans.
    A.9.2.9.3 Thus, in animal studies, when significant toxic effects are observed that indicate classification, consideration of the duration of experimental exposure and the dose/concentration at which these effects were seen, in relation to the suggested guidance values, provides useful information to help assess the need to classify (since the toxic effects are a consequence of the hazardous property(ies) and also the duration of exposure and the dose/concentration).
    A.9.2.9.4 The decision to classify at all can be influenced by reference to the dose/concentration guidance values at or below which a significant toxic effect has been observed.
    A.9.2.9.5 The guidance values refer to effects seen in a standard 90-day toxicity study conducted in rats. They can be used as a basis to extrapolate equivalent guidance values for toxicity studies of greater or lesser duration, using dose/exposure time extrapolation similar to Haber’s rule for inhalation, which states essentially that the effective dose is directly proportional to the exposure concentration and the duration of exposure. The assessment should be done on a case-by-case basis; for example, for a 28-day study the guidance values below would be increased by a factor of three.
    A.9.2.9.6 Thus for Category 1 classification, significant toxic effects observed in a 90-day repeated-dose study conducted in experimental animals and seen to occur at or below the (suggested) guidance values (C) as indicated in Table A.9.1 would justify classification:
    Table A.9.1: Guidance values to assist in Category 1 classification
    (applicable to a 90-day study)

    Route of exposure

    Units
    Guidance values
    (dose/concentration)
    Oral (rat)mg/kg body weight/dayC ≤ 10
    Dermal (rat or rabbit)mg/kg body weight/dayC ≤ 20
    Inhalation (rat) gasppmV/6h/dayC ≤ 50
    Inhalation (rat) vapormg/liter/6h/dayC ≤ 0.2
    Inhalation (rat) dust/mist/fumemg/liter/6h/dayC ≤ 0.02
    A.9.2.9.7 For Category 2 classification, significant toxic effects observed in a 90-day repeated-dose study conducted in experimental animals and seen to occur within the (suggested) guidance value ranges as indicated in Table A.9.2 would justify classification:
    Table A.9.2: Guidance values to assist in Category 2 classification
    (applicable to a 90-day study)

    Route of exposure

    Units
    Guidance values range
    (dose/concentration)
    Oral (rat)mg/kg body weight/day10 < C ≤ 100
    Dermal (rat or rabbit)mg/kg body weight/day20 < C ≤ 200
    Inhalation (rat) gasppmV/6h/day50 < C ≤ 250
    Inhalation (rat) vapormg/liter/6h/day0.2 < C ≤ 1.0
    Inhalation (rat) dust/mist/fumemg/liter/6h/day0.02 < C ≤ 0.2
    A.9.2.9.8 The guidance values and ranges mentioned in A.2.9.9.6 and A.2.9.9.7 are intended only for guidance purposes, i.e., to be used as part of the weight of evidence approach, and to assist with decisions about classification. They are not intended as strict demarcation values.
    A.9.2.9.9 Thus, it is possible that a specific profile of toxicity occurs in repeat-dose animal studies at a dose/concentration below the guidance value, e.g., < 100 mg/kg body weight/day by the oral route, however the nature of the effect, e.g., nephrotoxicity seen only in male rats of a particular strain known to be susceptible to this effect, may result in the decision not to classify. Conversely, a specific profile of toxicity may be seen in animal studies occurring at above a guidance value, e.g., ≥ 100 mg/kg body weight/day by the oral route, and in addition there is supplementary information from other sources, e.g., other long-term administration studies, or human case experience, which supports a conclusion that, in view of the weight of evidence, classification is prudent.
    A.9.2.10 Other considerations
    A.9.2.10.1 When a substance is characterized only by use of animal data the classification process includes reference to dose/concentration guidance values as one of the elements that contribute to the weight of evidence approach.
    A.9.2.10.2 When well-substantiated human data are available showing a specific target organ toxic effect that can be reliably attributed to repeated or prolonged exposure to a substance, the substance shall be classified. Positive human data, regardless of probable dose, predominates over animal data. Thus, if a substance is unclassified because no specific target organ toxicity was seen at or below the dose/concentration guidance value for animal testing, if subsequent human incident data become available showing a specific target organ toxic effect, the substance shall be classified.
    A.9.2.10.3 A substance that has not been tested for specific target organ toxicity may in certain instances, where appropriate, be classified on the basis of data from a scientifically validated structure activity relationship and expert judgment-based extrapolation from a structural analogue that has previously been classified together with substantial support from consideration of other important factors such as formation of common significant metabolites.
    A.9.3 Classification criteria for mixtures
    A.9.3.1 Mixtures are classified using the same criteria as for substances, or alternatively as described below. As with substances, mixtures may be classified for specific target organ toxicity following single exposure, repeated exposure, or both.
    A.9.3.2 Classification of mixtures when data are available for the complete mixture
    When reliable and good quality evidence from human experience or appropriate studies in experimental animals, as described in the criteria for substances, is available for the mixture, then the mixture shall be classified by weight of evidence evaluation of these data. Care shall be exercised in evaluating data on mixtures, that the dose, duration, observation or analysis, do not render the results inconclusive.
    A.9.3.3 Classification of mixtures when data are not available for the complete mixture: bridging principles
    A.9.3.3.1 Where the mixture itself has not been tested to determine its specific target organ toxicity, but there are sufficient data on both the individual ingredients and similar tested mixtures to adequately characterize the hazards of the mixture, these data shall be used in accordance with the following bridging principles as found in paragraph A.0.5 of this Appendix: Dilution; Batching; Concentration of mixtures; Interpolation within one toxicity category; Substantially similar mixtures; and Aerosols.
    A.9.3.4 Classification of mixtures when data are available for all ingredients or only for some ingredients of the mixture
    A.9.3.4.1 Where there is no reliable evidence or test data for the specific mixture itself, and the bridging principles cannot be used to enable classification, then classification of the mixture is based on the classification of the ingredient substances. In this case, the mixture shall be classified as a specific target organ toxicant (specific organ specified), following single exposure, repeated exposure, or both when at least one ingredient has been classified as a Category 1 or Category 2 specific target organ toxicant and is present at or above the appropriate cut-off value/concentration limit specified in Table A.9.3 for Category 1 and 2 respectively.
    Table A.9.3: Cut-off value/concentration limits of ingredients of a mixture classified as a
    specific target organ toxicant that would trigger classification of the mixture as Category 1 or 2


    Ingredient classified as:
    Cut-off values/concentration limits triggering classification of a mixture as:
    Category 1Category 2
    Category 1
    Target organ toxicant

    ≥ 1.0 %
     
    Category 2
    Target organ toxicant
     
    ≥ 1.0 %
    A.9.3.4.2 These cut-off values and consequent classifications shall be applied equally and appropriately to both single- and repeated-dose target organ toxicants.
    A.9.3.4.3 Mixtures shall be classified for either or both single- and repeated-dose toxicity independently.
    A.9.3.4.4 Care shall be exercised when toxicants affecting more than one organ system are combined that the potentiation or synergistic interactions are considered, because certain substances can cause specific target organ toxicity at < 1% concentration when other ingredients in the mixture are known to potentiate its toxic effect.


    A.10 ASPIRATION HAZARD
    A.10.1 Definitions and general and specific considerations
    A.10.1.1 Aspiration means the entry of a liquid or solid chemical directly through the oral or nasal cavity, or indirectly from vomiting, into the trachea and lower respiratory system.
    A.10.1.2 Aspiration toxicity includes severe acute effects such as chemical pneumonia, varying degrees of pulmonary injury or death following aspiration.
    A.10.1.3 Aspiration is initiated at the moment of inspiration, in the time required to take one breath, as the causative material lodges at the crossroad of the upper respiratory and digestive tracts in the laryngopharyngeal region.
    A.10.1.4 Aspiration of a substance or mixture can occur as it is vomited following ingestion. This may have consequences for labeling, particularly where, due to acute toxicity, a recommendation may be considered to induce vomiting after ingestion. However, if the substance/mixture also presents an aspiration toxicity hazard, the recommendation to induce vomiting may need to be modified.
    A.10.1.5 Specific considerations
    A.10.1.5.1 The classification criteria refer to kinematic viscosity. The following provides the conversion between dynamic and kinematic viscosity:
    Equation for conversion between dynamic and kinematic viscosity
    A.10.1.5.2 Although the definition of aspiration in A.10.1.1 includes the entry of solids into the respiratory system, classification according to (b) in table A.10.1 for Category 1 is intended to apply to liquid substances and mixtures only.
    A.10.1.5.3 Classification of aerosol/mist products
    Aerosol and mist products are usually dispensed in containers such as self-pressurized containers, trigger and pump sprayers. Classification for these products shall be considered if their use may form a pool of product in the mouth, which then may be aspirated. If the mist or aerosol from a pressurized container is fine, a pool may not be formed. On the other hand, if a pressurized container dispenses product in a stream, a pool may be formed that may then be aspirated. Usually, the mist produced by trigger and pump sprayers is coarse and therefore, a pool may be formed that then may be aspirated. When the pump mechanism may be removed and contents are available to be swallowed then the classification of the products should be considered.
    A.10.2 Classification criteria for substances
    Table A.10.1: Criteria for aspiration toxicity
    CategoryCriteria
    Category 1: Chemicals known to cause human aspiration toxicity hazards or to be regarded as if they cause human aspiration toxicity hazardA substance shall be classified in Category 1:
    (a) If reliable and good quality human evidence indicates that it causes aspiration toxicity (See note); or
    (b) If it is a hydrocarbon and has a kinematic viscosity ≤ 20.5 mm2/s, measured at 40° C.
    Note: Examples of substances included in Category 1 are certain hydrocarbons, turpentine and pine oil.
    A.10.3 Classification criteria for mixtures
    A.10.3.1 Classification when data are available for the complete mixture
    A mixture shall be classified in Category 1 based on reliable and good quality human evidence.
    A.10.3.2 Classification of mixtures when data are not available for the complete mixture: bridging principles
    A.10.3.2.1 Where the mixture itself has not been tested to determine its aspiration toxicity, but there are sufficient data on both the individual ingredients and similar tested mixtures to adequately characterize the hazard of the mixture, these data shall be used in accordance with the following bridging principles as found in paragraph A.0.5 of this Appendix: Dilution; Batching; Concentration of mixtures; Interpolation within one toxicity category; and Substantially similar mixtures. For application of the dilution bridging principle, the concentration of aspiration toxicants shall not be less than 10%.
    A.10.3.3 Classification of mixtures when data are available for all ingredients or only for some ingredients of the mixture
    A.10.3.3.1 A mixture which contains ≥ 10% of an ingredient or ingredients classified in Category 1, and has a kinematic viscosity ≤ 20.5 mm2/s, measured at 40 °C, shall be classified in Category 1.
    A.10.3.3.2 In the case of a mixture which separates into two or more distinct layers, one of which contains ≥ 10 % of an ingredient or ingredients classified in Category 1 and has a kinematic viscosity ≤ 20.5 mm2/s, measured at 40 °C, then the entire mixture shall be classified in Category 1.
    [77 FR 17790, March 26, 2012; 78 FR 9313, Feb. 8, 2013]
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