山东聊城市表层土壤有机氯农药残留研究

2008年麦收期间以网格布点法采集了聊城市137个土壤表层样品,利用ASE萃取技术,采用GC-ECD方法测定了样品中六六六（BHCs）、滴滴涕（DDTs）、六氯苯、艾氏剂、狄氏剂、异狄氏剂和七氯的检出率和残留量,并对土壤质量状况做了评价。结果表明,土壤中DDTs的检出率高达94.1％,其他6种有机氯农药（OCPs）均有不同程度检出。OCPs总残留量平均值为145.35μg／kg,其中DDTs占88.58％,是残留OCPs的主要成分。全部样点中BHCs的单因子污染指数Pi最大值为0.1,土壤未受BHCs污染;95％的样点中DDTs的Pi值小于1,土壤中DDTs含量未超标,而3％的样点Pi值小于2,土壤属轻度污染,2％的样点Pi值大于2,土壤属重度污染。     

QUALITY OF STORMWATER DRAINAGE FROM URBAN LAND1

ABSTRACT Urban storm water from a 1,067-acre drainage basin in Durham, N.C. was characterized to determine yield of pollutants. Population density averaged 9 persons per acre (ranging from <3 to 16). Annual BOD contribution attributable to surface wash during storms was determined to be approximately equal to contribution by its secondary wastewater treatment plant effluent. Total organic matter (COD) was estimated to exceed the amount in raw sanitary sewage from a residentially developed area of the same size. Mean basin yields (Ib/acre/day) were: BOD-0.23, COD-2.85, Total Solids-43.6, Volatile Total Solids-4.8, Total Phosphate-0.01 and Chloride-0.20 (as NaQ). The yield of lead presumed to originate from internal combustion engines operating on and near the basin was determined to be 0.006 Ib/acre/day. The concentration of total pesticides (Dieldrin; p,p'DDE; p,p-DDT; p,p'DDD and p,p'DDT) weighted for flow significance was estimated to be 1.2 parts per billion. The major long-term pollutional impact on a projected downstream reservoir was considered to be the fixed solids residue and long-term oxygen demand (COD). Intermittent release of other pollutants in slugs during runoff periods may be a significant factor in causing undesirable effects in streams draining urban areas.     

Residues of endosulfan and other selected organochlorine pesticides in farm areas of the Lower Fraser Valley, British Columbia, Canada

Crop soils, ditch sediments, and water flowing from several farm areas to salmon tributary streams of the Fraser River in the Lower Fraser Valley (LFV) of British Columbia, Canada, were sampled in 2002-2003 to quantify for residues of an organochlorine cyclodiene pesticide, endosulfan (END = alpha-endosulfan + beta-endosulfan + endosulfan sulfate). Residues from historical use of other selected organochlorine pesticides, namely, cyclodienes (aldrin, alpha-chlordane, gamma-chlordane, dieldrin, endrin, endrin aldehyde, heptachlor, and heptachlor epoxide), hexachlorocyclohexanes [alpha-benzene-hexachloride (alpha-BHC), beta-BHC, delta-BHC, and gamma-BHC (lindane)], and DDT-related compounds (p,p-DDT, p,p-DDD, p,p-DDE, and methoxychlor) were also determined. Reference and background levels of these pesticides in ditches leading to fish streams were obtained from pristine watershed areas. Varying amounts of END residues were detected in soils (<0.02-5.60 mg kg(-1) dry wt.) and ditch sediments (<0.02-3.33 mg kg(-1) dry wt.) in mainly three of five farm areas sampled. Likewise, residues (excluding END) of other selected organochlorine compounds such as aldrin, BHC, chlordane, endrin, p,p-DDT, methoxychlor, and their respective major transformation products (endosulfan sulfate, dieldrin, endrin aldehyde, heptachlor, heptachlor epoxide, p,p-DDD, and p,p-DDE) were found in crop soils (<0.02-16.2 mg kg(-1) dry wt.) and sediments (<0.02-9.73 mg kg(-1) dry wt.). Most of these pesticides (END: <0.01-1.86 microg L(-1); other selected organochlorine pesticides: <0.0.1-1.50 microg L(-1)) were also found in ditch water leading to salmon streams in several farms. The END levels of crop soils from the same LFV study farms in 1994 and 2003 indicated an estimated decline of 22% to 1.35 mg kg(-1) dry wt. during that period. This reduction was probably due to the increasing use of alternate pesticides (e.g., organophosphorus compounds). Some possible biological implications of these pesticide residues on nontarget organisms in the LFV are discussed.     

Adsorption of Pb and Cd on the natural surface coatings (NSCs) in the presence of organochlorine pesticides: a preliminary investigation

Adsorption of Pb and Cd in the presence and absence of organochlorine pesticides (OCPs) on natural surface coatings (NSCs), which were collected in the Nanhu Lake in Changchun, China, was measured in order to investigate the effect of the OCPs on the adsorption of heavy metals on the NSCs. Adsorption of Pb/Cd was carried out under controlled laboratory conditions (mineral salt solution with defined species, ionic strength 0.05 mol/l, 25 degrees C and pH 6.0) with initial Pb and Cd concentrations ranging from 0.2 to 2.5 mol/l. The classical Langmuir adsorption isotherm was applied to estimate the equilibrium coefficients of the adsorption of Pb and Cd on the NSCs. Adsorption interference between Pb/Cd and the OCPs on the NSCs indicated that the adsorption of Pb/Cd on the NSCs was influenced by the OCPs, and competitive adsorption between Pb and the OCPs was observed while adsorption of Cd was enhanced by addition of the OCPs. Adsorption data fit the Langmuir isotherm well for the NSCs treated with the OCPs at different equilibrium concentrations. The results showed that the amount of adsorbed Pb decreased by more than 40% while the amount of adsorbed Cd increased by over 60% with an increase in the initial concentrations of the OCPs ranging from 0 to 5.0 microg/l and that adsorption of Pb/Cd on the NSCs was strongly affected by the OCPs. This preliminary study highlights the importance of the OCPs on the NSCs in controlling the transport, fate, biogeochemistry, bioavailability and toxicity of trace metals in aquatic environments.     

汕头地区农业生态系统中有机氯农药的研究

有机氯农药（Organochlorine Pesticides,OCPs）是一类由人工合成的杀虫广谱、毒性较低、残效期长的化学杀虫剂。本文以汕头市为研究区域,探讨了土壤OCPs的残留现状和特征,并对该区的土壤进行了环境质量评价和初步的生态风险评价。结果表明：（1）汕头地区土壤中OCPs的检出率高达99.13％,OCPs残留量的平均值是113.37 ng·g^-1,主要的OCPs污染物为DDTs和硫丹类;南澳县OCPs残留量平均值最高（174.68 ng·g^-1）,其次为龙湖区,濠江区含量平均值最低（69.24 ng·g^-1）;（2）与国内外一些地区土壤中OCPs的残留量对比,本研究区域土壤中的OCPs处于中等污染残留水平;与美国马里兰州标准、纽约州可容许的土壤浓度标准和我国的土壤环境质量标准相比较,OCPs基本没有超标;（3）本研究地区土壤存在较高的生态风险,OCPs可能对环境造成一定的危害,其中生态风险最高的是DDTs,BHCs的生态风险较低。     

An intergrated waste survey and environmental effects of COGIDO, a bleached pulp and paper mill in Vietnam, on the receiving waterbody

An integrated investigation on wastewater characterization and the environmental effects from the COGIDO pulp and paper mill in Bien Hoa Industrial Estate, Vietnam, a chlorine bleached soda integrated pulp and paper mill operating without a chemical recovery system, on the receiving water body was conducted during the rainy and dry seasons in 1993 and 1995. The pollution load from the mill was very high in terms of BOD, COD and SS (COD_m: 58.7 t/d; BOD: 33.3 t/d and SS: 25.1 t/d). The effluent toxicity was determined using four toxicity tests: the green micro-alga, Selenastrum capricornutum, Microtox (marine bacteria: Photobacterium phosphoreum), the duckweed, Lemna aequinoctialis, and fish (silver barb: Puntius gonionotus, and Tilapia: Tilapia nilotica). Selenastrum capricornutum was the most sensitive among the tested organisms. The mill toxicity emission rate (TER) was as high as 338 610 (Selenastrum test). The bleaching-pulp and semi-chemical pulp plants which contributed the largest pollution load to the total COGIDO effluent, therefore, were targeted for abatement measures. Physico-chemical parameters as well as qualitative and quantitative aquatic organism composition for the river water were established. The BOD₅ and COD values exceeded the potable surface water standard by a factor of 2 to 4. The species diversity and abundance of the phytoplankton, zooplankton and zoobenthos were found to be lower (20–40%) than that of unpolluted rivers in Vietnam, whereas pollution-indicator species increased up to four times during the dry season 1995.     

浅谈串联四极杆质谱（GC—QqQ-MS／MS）在土壤样品有机污染物分析中的应用

建立了ASE-GPC—GC-QqQ—MS／MS测定土壤中17种有机氯农药和19种多氯联苯以及MAE-SPE—GC-QqQ—MS／MS测定土壤中16种多环芳烃和18种邻苯二甲酸酯的方法。多环芳烃和邻苯二甲酸酯定量限在0．02～2．81μg／kg之间,有机氯农药和多氯联苯定量限在0．01～0．51μg/kg之间。样品加标浓度在5μg/kg时多环芳烃和邻苯二甲酸酯的平均回收率在66．6％～122．1％之间,相对标准偏差均小于20％;有机氯农药和多氯联苯平均回收率在79．6％～93．2％之间,相对标准偏差均小于15％。     

静态条件下持续时间对底泥中有机氯农药释放的影响

有机氯农药是广泛存在于环境中一类有机污染物,溶解度低,疏水性强,容易被颗粒物吸附,并随其在沉积物中积累,蓄积在沉积物中的有机氯农药在沉积物的再悬浮过程中会重新释放进入水体,造成二次污染。为了考察悬浮持续时间对沉积物中有机氟农药的释放的影响,采用沉积物释放模拟装置在60天内对微山湖沉积物中有机氯农药释放进行研究。结果表明,随着扰动时间的延长,上覆水中有机氯农药的含量在0—20天内增长很快,在60天左右含量趋于到稳定。不同的有机氟农药在扰动条件下,释放的速率和浓度是不一样的,其中水溶性大的农药更易向水体再次释放。     

Fate of pesticides in combined paddy rice-fish pond farming systems in northern Vietnam

During the last decades, high population growth and export-oriented economics in Vietnam have led to a tremendous intensification of rice production, which in turn has significantly increased the amount of pesticides applied in rice cropping systems. Since pesticides are toxic by design, there is a natural concern on the impact of their presence in the environment on human health and environmental quality. The present study was designed to examine the water regime and fate of pesticides (fenitrothion, dimethoate) during two consecutive rice crop seasons in combined paddy rice-fish pond farming systems in northern Vietnam. Major results revealed that 5 and 41% (dimethoate), and 1 and 17% (fenitrothion) of the applied mass of pesticides were lost from the paddy field to the adjacent fish pond during spring and summer crop seasons, respectively. The decrease of pesticide concentration in paddy surface water was very rapid with dissipation half-life values of 0.3 to 0.8 and 0.2 d for dimethoate and fenitrothion, respectively. Key factors controlling the transport of pesticides were water solubility and paddy water management parameters, such as hydraulic residence time and water holding period. Risk assessment indicates that the exposure to toxic levels of pesticides for aquaculture (, ) is significant, at least shortly after pesticide application.     

Micro-trench experiments on interflow and lateral pesticide transport in a sloped soil in northern Thailand

During recent decades, a change in land use in the mountainous regions of Northern Thailand has been accompanied by an increased input of agrochemicals. We identified lateral water flow and pesticide transport pathways and mechanisms in a Hapludult on a sloped litchi orchard in Northern Thailand. During two rainy seasons, two micro-trench experiments were performed at the plot scale (2 by 3 m). The first experiment was performed at the footslope of the orchard; the second was performed at a midslope position. Two salt tracers (bromide and chloride) and two pesticides {methomyl [S-methyl-N-(methylcarbamoyloxy)thioacetimidate] and chlorothalonil (2,4,5,6-Tetrachlor-1,3-benzdicarbonitril)} were applied in stripes parallel to the slope 150 and 300 cm away from the trench. At the trench, soil water was collected by wick samplers. Tensiometers and time-domain reflectometry probes were installed. At the end of the experiment, soil samples were taken and analyzed for residual concentrations of tracers and pesticides. Lateral subsurface flow of water occurred exclusively along preferential flow paths and was mainly observed at 0- to 30- and 60- to 90-cm depth. Lateral transport of pesticides was negligible, but both pesticides were found beneath the application area at 90 cm depth. Therefore, they may pose a groundwater contamination risk. The amount of wick flow and the location of interflow were mainly a function of rain amount and antecedent soil water suction. During dry periods, water flow was restricted to the topsoil. After heavy rain events and wet periods, interflow was mainly observed in the subsoil. The cumulative rain amount between samplings necessary to induce interflow was 20 mm. At the footslope, the interflow was seven times higher, and the network of water-bearing pores increased compared with the midslope position.     

Effects of chaotic acclimation applied on performance of microbial fuel cells

Microbial fuel cells (MFCs) are one of the bioreactors that produce electrons by metabolizing substrate from microorganisms, and have the ability to both degrade waste solution and produce electrons. Recently, the activity of microorganisms has limited the power performance of MFCs. Chaos has been used to stimulate activity of microorganisms, but it has not been used previously in MFCs. In this study, three types of acclimations – native acclimation (NA), MFC acclimation (MFCA), and MFC embedded with chaotic electric field acclimation (CMFCA) – are applied to realize their performance and chemical oxygen demand (COD) removal in MFCs, respectively. Results show that the current density and the power density of CMFCA were improved by 1.33 and 1.25 times than MFCA, and the COD removal of CMFCA reached 85% after five days. In addition, the acclimation stage at the condition of CMFCA appeared after 10 days, but was not found for the MFCA system. These observations would provide positive information for improving the performance of MCFs in the future.     

TRANSPORT OF SEDIMENT-BOUND ORGANOCHLORINE PESTICIDES TO THE SAN JOAQUIN RWER,CALIFORNIA1

ABSTRACT: Suspended sediment samples were collected in west-side tributaries and the main stem of the San Joaquin River, California, in June 1994 during the irrigation season and in January 1995 during a winter storm. These samples were analyzed for 15 organochiorine pesticides to determine their occurrence and their concentrations on suspended sediment and to compare transport during the irrigation season (April to September) to transport during winter storm runoff (October to March). Ten organochiorine pesticides were detected during the winter storm runoff; seven during the irrigation season. The most frequently detected organochlorine pesticides during both sampling periods were p,p'-DDE, p,p'-DDT, p,p'-DDD, dieldrin, toxaphene, and chiordane. Dissolved samples were analyzed for three organochiorine pesticides during the irrigation season and for 15 during the winter storm. Most calculated total concentrations of p,p-DDT, chlordane, dieldrin, and toxaphene exceeded chronic criteria for the protection of freshwater aquatic life. At eight sites in common between sampling periods, suspended sediment concentrations and streamfiow were greater during the winter storm runoff - median concentration of 3,590 mg/L versus 489 mg(L and median streamfiow of 162 ft³/s versus 11 ft³/s. Median concentrations of total DDT (sum of p,p'-DDD, p,p-DDE, and p,p'-DDT), chlordane, dieldrin, and toxaphene on suspended sediment were slightly greater during the irrigation season, but instantaneous loads of organochlorine pesticides at the time of sampling were substantially greater during the winter storm. Estimated loads for the entire irrigation season exceeded estimated loads for the January 1995 storm by about 2 to 4 times for suspended transport and about 3 to 11 times for total transport. However, because the mean annual winter runoff is about 2 to 4 times greater than the runoff during the January 1995 storm, mean winter transport may be similar to irrigation season transport. This conclusion is tentative primarily because of insufficient information on long-term seasonal variations in suspended sediment and organochlorine concentrations. Nevertheless, runoff from infrequent winter storms will continue to deliver a significant load of sediment-bound organochiorine pesticides to the San Joaquin River even if irrigation-induced sediment transport is reduced. As a result, concentrations of organochlorine pesticides in San Joaquin River biota will continue to be relatively high compared to other regions of the United States.     

新都县水污染总量控制实施研究

实施水污染总量控制,是我国在新的历史条件下污染控制战略的重大转变,也是今后环境管理工作的主要的技术手段。本文以成都市卫星城新都县为例,分析了辖区内污染物的来源和排放情况、建立环境质量与污染源分布的定量响应关系、测算区域环境容量的大小,并将总量控制的削减指标落实到主要的污染源。实施水污染总量控制的方法和措施的研究,不仅为新都县实行总量控制提供了科学依据,而且对其它中小区域也具有借鉴意义。     

混凝沉降法处理洗衣废水的实验研究

洗涤废水含有表面活性剂和磷酸盐物质,直接排入水体会造成水体的污染,增加给水处理厂的处理难度,甚至会引起水体富营养化。本实验是通过投加PAC和PAM絮凝沉降联合活性炭吸附来处理商业洗涤废水,以去除废水中的COD。实验表明：采用PAC PAM 活性炭工艺处理洗衣废水的效果较好,投药过程COD的去除率可以达到60％以上,经过活性炭过滤后,总的去除率可以达到86％。出水ODD可以降至在50mg／L左右。     

多项膜生物反应器在含盐废水处理中的应用

文章介绍了哈尔滨石化公司应用多项膜生物反应器处理炼化企业含盐废水。影响膜生物反应器的主要运行参数有电导率、溶解氧、COD,电导率适宜范围是3000～5000μS/cm,大于6000μS/cm微生物受到抑制,低于2000μS/cm时,去除率显著下降;一级好氧单元溶解氧适宜范围4.2～7.0mg/L或2.0～3.0mg/L,分别是好氧微生物和兼性微生物占据优势;当进水COD低于500mg/L,出水可稳定达到GB8978-1996《污水综合排放标准》二级标准(COD≤120mg/L)。     

The effect of Oja-titun market effluent on the chemical quality of receiving OPA reservoir in Ile-Ife, Nigeria

The effect of market effluent from the Oja-titun market in Ile-Ife, Nigeria on the chemical quality of the Opa Reservoir located 3.5 km downstream was investigated between February and November 2000. Water samples were collected in February, May, August and November from 16 sites, four along each of the market drainage channels (MDC), market stream, tributary stream and the Opa River and Reservoir. The peak level of each variable-biochemical oxygen demand, temperature, total alkalinity, Na(+), K(+), Ca(2+), Mg(2+), PO(4)(3+), SO(4)(2+), Cl(-), NO(3)(-), Pb and Zn-occurred at the MDC, and decreased significantly downstream, except pH, conductivity and dissolved oxygen, which increased. Seasonal fluctuation in most variables was pronounced. Generally, there were high values in the early dry and dry seasons and low values in the rainy and early rainy seasons. Comparison of the reservoir water with international limitation standards for drinking water supply showed that the quality of the reservoir water was very low and that treatment required to achieve minimum limitation standards for drinking water would be both intensive and expensive. The study concluded that the stream borne effluent from the market impacts significantly on the chemical quality of the reservoir water although other tributaries within the Reservoir's catchment are other possible sources of pollutants in the reservoir.     

Optimization of Fenton's oxidation of chemical laboratory wastewaters using the response surface methodology

Establishing a treatment process for practical and economic disposal of laboratory wastewaters has become an urgent environmental concern of the Department of Chemical Engineering of the Universidade Estadual de Maringá (State University of Maringá), Brazil. Fenton and related reactions are potentially useful oxidation processes for destroying toxic organic compounds in water. In these reactions, hydrogen peroxide is combined with ferrous or ferric iron in the presence or absence of light to generate hydroxyl radicals (.OH). The feasibility of Fenton's reagent to treat waste chemicals from an academic research laboratory was investigated in this study. A response surface methodology was applied to optimize the Fenton oxidation process conditions using chemical oxygen demand (COD) removal as the target parameter to optimize, and the reagent concentrations, as related to the initial concentration of organic matter in the effluent, and pH as the control factors to be optimized. Maximal COD removal (92.3%) was achieved when wastewater samples were treated at pH 4 in the presence of hydrogen peroxide and iron in the ratios [COD]:[H2O2]=1:9 and [H2O2]:[Fe2+]=4.5:1. Under these conditions, it was possible to obtain simultaneously maximal COD removal and minimal chemical sludge after treatment, which is a residue that needs further processing.     

BATCH REACTOR UNVEGETATED WETLAND PERFORMANCE IN TREATING DAIRY WASTEWATER1

ABSTRACT: Wetlands that treat holding pond effluent can be designed to utilize the pond storage capacity to allow flexibility in system management. Management of a wetland as a sequencing batch reactor can simplify operation and control detention times, but little performance data on such systems are available. The objective of this study was to evaluate the batch reactor wetland concept by quantifying removal of chemical oxygen demand (COD), total suspended sediments (TSS), total nitrogen (TN), ammonium (NH₄), nitrate (NO₃), total phosphorus (TP), and orthophosphate (PO₄) and by assessing the suitability of first‐order kinetics. Weekly samples were collected following batch loadings of wetland cells with high concentration or low concentration dairy holding pond wastewater during both fall and spring seasons. During three‐week batch periods without plants, overall mass removal averaged 54 percent for COD, 58 percent for TSS, 90 percent for TN, 72 percent for NH₄, ‐54 percent for NO₃, 38 percent for TP, and ‐8 percent for PO₄. Best fit, first‐order kinetic rate constant (k) and background concentration (C*) for COD varied by season, with k = 0.024/d and C*= 0 mg/l in fall and k = 0.056/d and C*= 200 mg/l in spring. Ammonium exhibited a consistent C*= 0 mg/l but had variable rate constants of k = 0.121/d for low concentration treatments and k = 0.079/d for high concentration treatments. Using first‐order kinetics was also appropriate for TN, with k = 0.061/d and C*= 0 mg/l for all loadings and seasons, but was not consistently appropriate for TP or PO₄. These results support the use of first‐order kinetics to describe treatment in batch reactor wastewater treatment wetlands without vegetation, perhaps during the establishment phase or in open water zones of vegetated wetlands. Further work is needed to assess the effects of vegetation.     

Biological alkylation and colloid formation of selenium in methanogenic UASB reactors

Bioalkylation and colloid formation of selenium during selenate removal in upflow anaerobic sludge bed (UASB) bioreactors was investigated. The mesophilic (30 degrees C) UASB reactor (pH = 7.0) was operated for 175 d with lactate as electron donor at an organic loading rate of 2 g COD L(-1) d(-1) and a selenium loading rate of 3.16 mg Se L(-1) d(-1). Combining sequential filtration with ion chromatographic analysis for selenium oxyanions and solid phase micro extraction gas chromatography mass spectrometry (SPME-GC-MS) for alkylated selenium compounds allowed to entirely close the selenium mass balance in the liquid phase for most of the UASB operational runtime. Although selenate was removed to more than 98.6% from the liquid phase, a less efficient removal of dissolved selenium was observed due to the presence of dissolved alkylated selenium species (dimethylselenide and dimethyldiselenide) and colloidal selenium particles in the effluent. The alkylated and the colloidal fractions contributed up to 15 and 31%, respectively, to the dissolved selenium concentration. The size fractions of the colloidal dispersion were: 4 to 0.45 mum: up to 21%, 0.45 to 0.2 mum: up to 11%, and particles smaller than 0.2 mum: up to 8%. Particles of 4 to 0.45 mum were formed in the external settler, but did not settle. SEM-EDX analysis showed that microorganisms form these selenium containing colloidal particles extracellularly on their surface. Lowering the temperature by 10 degrees C for 6 h resulted in drastically reduced selenate removal efficiencies (after a delay of 1.5 d), accompanied by the temporary formation of an unknown, soluble, organic selenium species. This study shows that a careful process control is a prerequisite for selenium treatment in UASB bioreactors, as disturbances in the operational conditions induce elevated selenium effluent concentrations by alkylation and colloid formation.     

Insecticide pollution of Indian rivers

Summary Rivers are the main source of water in India, and are particularly used for agricultural irrigation and drinking water supply. As most of the rivers pass through agricultural fields, they are subject to contamination with the different insecticides used for crop protection. Residues of persistent organochlorines, which are still used in large quantities in India, are found in water from many Indian rivers. In certain rivers, the concentrations of DDT, aldrin and heptachlor are often present in excess of their guideline limits. Although the concentration level of gamma-HCH is well below the guideline limit, the accumulation of the carcinogenic beta isomer is a matter of great concern. A few organophosphorus insecticides have also been detected in river water. Recently, some organochlorine insecticides have been banned from use in India. The use of new, readily biodegradable insecticides and biocides in agriculture and public health programmes offers some optimism.Drs Satya P. Mohapatia, Vijay T. Gajbhiye and Narendra R. Agnihotri all work within the Division of Agricultural Chemicals at the above address. Dr Manju Raina is employed by the Ganga Project Directorate of the Ministry of Environment and Forests, New Delhi 11003, India.