Pollution assessment of organochlorine pesticides in urban agricultural soils of Jilin City,China

The content, source, and pollution level of organochlorine pesticides (OCPs) in soils are necessary to assess potential risks to eco-environment and human health, and to target environment-friendly policies. A total of 50 surface soil samples were collected from urban vegetable fields of Jilin City and thirteen OCPs were analyzed. The concentrations were in the ranges of 3.16–48.35 ng·g^?1 for Dichloro-Diphenyl-Tricgloroethanes (DDTs, sum of o, p′-DDT, p, p′-DDT, p, p′-DDD, and p, p′-DDE), 4.37–44.77 ng·g^?1 for Hexachlorocyclohexanes (HCHs, sum of α-HCH, β-HCH, γ-HCH, and δ-HCH), 1.19–13.17 ng·g^?1 for Chlordanes (sum of heptachlor, t-chlordane, and c-chlordane), 0.24–2.60 ng·g^?1 for aldrin, and nd–3.43 ng·g^?1 for dieldrin, respectively. The different compositions indicated that the residues of DDTs and HCHs originated mainly from the historical application, while chlordanes were mostly from recent input. On the basis of soil quality standards of China and the Netherlands, DDTs and chlordanes in this study were categorized as light pollution, and HCHs were classified as no pollution for the majority of soil samples. There are a variety of OCPs residues in urban vegetable soils of Jilin City, but it is still safe and suitable for agricultural production.     

南亚热带典型地区农业土壤中多环芳烃和有机氯农药研究

参考美国EPA标准方法对南亚热带潮汕地区农业土壤中持久性有机污染物多环芳烃（PAHs）和有机氯农药（OCPs）进行分析,并对其分布和来源进行研究,最后探讨了不同种植方式下污染物的污染特征。结果表明：该区农业土壤中PAHs含量范围从22．1ng／g到1256．9ng／g,与其它地区的污染程度和一些土壤环境质量标准相比,该区处于中等污染水平。高温裂解是土壤PAHs的主要来源。OCPs在被禁止20a后在土壤中仍有残留,残留水平从4．6ng／g到1021．5ng／g,其中HCHs和DDTs的残留未超过国家土壤环境质量标准。早期使用残留是其主要污染源,但新近仍有DDT和硫丹的输入。PAHs和OCPs的污染主要集中在土壤表层和亚表层,且随着深度的加深,污染逐渐减少,但40cm以下,污染变化很小。菜地土壤PAHs污染水平低于稻田土壤,而OCPs污染水平高于稻田土壤。     

Ecotoxicological Risk Assessment of Polychlorinated Biphenyls (PCBs) in Bank Sediments from along the Yamuna River in Delhi,India

The River Yamuna originates from the Yamunotri glacier of the Himalayas and travels 22 km in the Delhi region. The river is used for various purposes in Delhi including drinking water supply. Twenty-eight polychlorinated biphenyls (PCBs) congeners were measured in bank sediments along the river, and their ecotoxicological risk was evaluated. Concentrations of ∑28PCBs varied from 0.20–21.16 ng g^?1 (dry wt.) with mean and median values of 6.63 ng g^?1 and 5.84 ng g^?1 (±0.69 ng g^?1), respectively. The concentration of 12 dl-PCBs concentrations varied from 0.04–2.86 ng g^?1 with a mean of 1.04 ± 0.11 ng g^?1, and their toxic equivalency ranged between <0.01–28.67 pg WHO-TEQ g^?1 with a mean of 10.77 ± 1.06 pg WHO-TEQ g^?1. CB-37, CB-44, CB-114, and CB-118 congeners were dominant among all PCBs congeners. The tri-PCBs (49%) were the main contributors to the PCB homolog followed by tetra-PCBs (35%), and penta-PCB (14%). Because there are no environmental guidelines in India for PCBs in river and marine sediments, concentrations of PCBs and their toxic equivalents were compared in a screening-level assessment with established freshwater sediment quality guidelines and found lower than those guideline values, which suggests no adverse ecotoxicological effect.     

巢湖表层水体中有机氯农药的分布及其组成

以固相萃取-气相色谱法/电子捕获检测器(SPE-GC/ECD)作为检测手段,对巢湖表层水体中有机氯农药(OCPs)的分布及组成特征进行分析.结果表明:研究区13个采样点中共检出包括六六六(HCHs)、滴滴涕(DDTs)、β-硫丹(β-Endosulfan)、艾氏剂(Aldrin)、六氯苯(hexachlorobenzene)和七氯(Heptachlor)在内的16种有机氯农药,其总含量范围为0.54～64.01ng.L-1;16种有机氯农药中以HCHs和DDTs为主,其平均质量浓度分别为5.56ng.L-1和16.57ng.L-1,约占其总量的84.75%;研究区的有机氯农药污染除了主要源于历史上农田中有机氯农药的残留外,近期可能还有新的农药污染源进入水环境;研究区所检出的各类有机氯农药均未超过国家地表水环境质量标准,巢湖表层水体中有机氯农药含量及潜在风险均属于中等偏低水平.     

Distribution of organochlorines and ecological risks in surface sediments from El-Mex Bay,Mediterranean Sea

Polychlorinated biphenyls (PCBs) and organochlorine pesticides (OCPs) were determined in eight sampling sites collected from El-Mex Bay sediments during the period of 2013–2015. Concentrations of PCBs, Hexachlorocyclohexanes (HCHs), Dichloro Diphenyl Trichloroethanes (DDTs), and cyclodienes ranged from 0.148 to 23.99, ND to 0.089, ND to 4.64, and 0.005 to 0.581 ng g^?1 dry wt, respectively. Total organic carbon (TOC) was relatively low, ranging from 0.09% to 1.42%. Total carbonate content ranged from 38% to 58%. The negative correlation of TOC with total pesticides (r = ?0.18) suggested that TOC does not have a role binding with pesticides. On the other hand, a positive correlation between PCBs and TOC (r = 0.254 at p > 0.01) was observed probably due to the low solubility of PCBs in the seawater. So, it will continue to precipitate until it reaches the bottom water and contaminates the sediment. The data obtained in the present work compared well with the counterpart data reported internationally. In general, the results of PCBs and OCP concentrations in El-Mex Bay sediments were much lower than the permissible levels recorded by sediment quality guidelines (SQGs). Interestingly, the organochlorines in sediments of El-Mex Bay were below the respective SQG values and were not likely to pose potential biological adverse impact.     

Characterization,source apportionment,and human health risk assessment of polycyclic aromatic hydrocarbons (PAHs) in road dust of a small island state in the Caribbean

Sixty-four and fifty-six road dust samples were collected over two seasons from various locations throughout the island of Trinidad and analyzed for the 16 priority PAHs. Total PAH concentrations ranged from 21 ng g^?1 to 4723 ng g^?1 (d.w.) for the rainy season and 36 ng g^?1 to 2428 ng g^?1 (d.w.) for the dry season. The Σ4–6 ring PAHs accounted for 88% and 63% of the 16 PAHs in road dust samples for the rainy and dry seasons, respectively. PAH diagnostic ratios, principal component analysis, and cluster analysis revealed both pyrogenic and petrogenic sources in road dust for the two seasons, with major contributions from vehicular emissions. Contributions from incomplete combustion and petroleum sources were also identified. The estimated Incremental Lifetime Cancer Risk (ILCR) associated with exposure to road dust PAHs in Trinidad for the rainy and dry seasons indicated no potential risk for both children and adults, as denoted by ILCR values lower than 10^?6.     

Organochlorine Pesticides in Sediments around Chaohu Lake: Concentration Levels and Vertical Distribution

Eighteen organochlorine pesticides (OCPs) were investigated in surface sediments from the Nanfei River and in four sediment cores from the primary estuaries of Chaohu Lake, Eastern China. The results indicate that the OCP concentrations in the surface and core sediments around Chaohu Lake were 3.48–121.08 (with a mean of 34.93) ng/g and 0.60–39.28 (7.07) ng/g, respectively. Significantly higher concentrations of ΣOCPs were observed in sediment samples from the Nanfei River and its estuary. The three important OCP contributors around Chaohu Lake were dichlorodiphenyltrichloroethane and its metabolites (DDTs), hexachlorocyclohexane isomers (HCHs), and hexachlorobenzene (HCB), which originated primarily from the historical use of technical DDTs and HCHs. A principal component analysis (PCA) suggests that HCB and lindane may originate from the same sources, and DDTs were greatly influenced by organic carbon from the soil environment and the impact of urbanization processes.     

Bioaccessibility-Based Risk Assessment of PAHs in Soils from Sites of Different Anthropogenic Activities in Lagos,Nigeria Using the Fed Organic Estimation Human Simulation Test Method

The aim of this study was to carry out a bioaccessibility-based risk assessment of polycyclic aromatic hydrocarbons (PAHs) in soils from sites of different anthropogenic activities in Lagos, Nigeria. Using an in vitro gastrointestinal model—Fed Organic Estimation Human Simulation Test method (FOREShT), the concentration of bioaccessible 16 priority US Environmental Protection Agency (USEPA) PAHs in soils were determined. Total concentration of 16 priority USEPA PAHs was also determined. The concentration range was 702–253,922 ng g^?1 and 92–760 ng g^?1 for total and bioaccessible PAHs, respectively. For persons involved with activities at these sites no health risks were observed, based on bioaccessibility values of PAHs. Mean daily intake of PAHs from these soils were below the oral mean daily intake threshold for PAHs in food. Also, overall estimated theoretical cancer risk (2.5 × 10^?09, 6.5 × 10^?07, 5.5 × 10^?10, 2.7 × 10^?09, 6.5 × 10^?10, 9.5 × 10^?10, 2.0 × 10^?09, and 4.1 × 10^?07 for the eight sites based on their bioaccessible concentration) for exposure to PAHs in surface soils were below the health guidelines for extreme (1 × 10^?04) and normal (1 × 10^?06) exposures.     

Heavy Metals Bioconcentration from Soil to Vegetables and Assessment of Health Risk Caused by Their Ingestion

The present study was undertaken to assess the non-carcinogenic human health risk of heavy metals through the ingestion of locally grown and commonly used vegetables viz. Raphanus sativus (root vegetable), Daucus carota (root vegetable), Benincasa hispida (fruit vegetable) and Brassica campestris leaves (leafy vegetable) in a semi-urbanized area of Haryana state, India. Heavy metal quantification of soil and vegetable samples was done using flame atomic absorption spectrophotometer. Lead, cadmium and nickel concentration in vegetable samples varied in range of 0.12–6.54 mg kg^?1, 0.02–0.67 mg kg^?1 and <0.05–0.41 mg kg^?1, respectively. Cadmium and lead concentration in some vegetable samples exceeded maximum permissible limit given by World Health Organization/Food and Agriculture Organization and Indian standards. Much higher concentrations of Pb (40–190.5 mg kg^?1), Cd (0.56–9.85 mg kg^-1) and Ni (3.21–45.87 mg kg^?1) were reported in corresponding vegetable fields’ soils. Correlation analysis revealed the formation of three primary clusters, i.e. Cu–Cd, Cd–Pb and Ni–Zn in vegetable fields’ soils further supported by cluster analysis and principal component analysis. Bioconcentration factor revealed that heavy metals’ uptake was more by leafy vegetable than root and fruit vegetables. Hazard index of all the vegetables was less than unity; thus, the ingestion of these vegetables is unlikely to pose health risks to the target population.     

PAH contamination in road dust from a moderate city in North China: The significant role of traffic emission

To investigate the contamination level, distribution, possible source, and human exposure risk of polycyclic aromatic hydrocarbons (PAHs) in the urban traffic environment, 15 PAHs were measured in 34 road dust samples (particle size < 25 μm) collected from three grades of roads and park paths in Xinxiang, China. ΣPAHs concentrations ranged from 311 to 21200 ng g^?1, with a mean of 5890 ng g^?1 and decreased in the following order: main roads (7650 ng g^?1) > collector streets (7410 ng g^?1) > bypasses (2970 ng g^?1) > park paths (1570 ng g^?1), indicating that significant positive correlation existed between PAH contamination and traffic density. PAHs in all samples were dominantly composed of 4-ring PAHs, accounting for 44.8% of the total. Pyrene, fluoranthene, and chrysene were the predominant individual components and accounted for 14.7% (1.2–19.2%), 12.9% (3.3–20.3%), and 11.0% (2.5–18.6%) of ΣPAHs, respectively. The specific isomer ratios indicated that traffic emission was the dominant source of PAHs in road dust. The incremental lifetime cancer risk values showed that cancer risk from exposure to road dust–borne PAHs was acceptable for local residents in Xinxiang.     

宁波滩涂贝类养殖区沉积物中有机氯农药和多氯联苯残留及生态风险评估

利用GC-ECD对宁波市主要滩涂贝类养殖区表层沉积物中的多氯联苯(PCBs)和有机氯农药六六六(HCHs)、滴滴涕(DDTs)的残留量进行测定,研究其分布状况,并进行生态风险评估.结果表明:贝类养殖区表层沉积物中的总有机氯农药含量为0.80～32.40ng·g-1,多氯联苯含量为3.20～33.33 ng·g-1.HCHs主要来自远距离大气传输及历史残留,部分区域有DDTs输入,其来源可能是三氯杀螨醇的使用.大部分站位的p,p’-DDT和DDTs存在潜在的生态风险,其中墙头和西店海域的p,p’-DDT残留超过生物效应中值,对底栖生物毒害效应较高.大多数站位PCBs的生态风险较低.     

The detection of food soils on stainless steel using energy dispersive X-ray and Fourier transform infrared spectroscopy

Organic soiling is a major issue in the food processing industries, causing a range of biofouling and microbiological problems. Energy dispersive X-ray (EDX) and Fourier transform infra red spectroscopy (FT-IR) were used to quantify and determine the biochemical groups of food soils on stainless steel surfaces. EDX quantified organic material on surfaces where oily based residues predominated, but was limited in its usefulness since other food soils were difficult to detect. FT-IR provided spectral ‘fingerprints’ for each of the soils tested. Key soiling components were associated with specific peaks, viz. oils at 3025 cm^?1–3011 cm^?1, proteins at 1698 cm^?1–1636 cm^?1 and carbohydrates at 1658 cm^?1–1596 cm^?1, 783 cm^?1–742 cm^?1. High concentrations of some soils (10%) were needed for detection by both EDX and FT-IR. The two techniques may be of use for quantifying and identifying specific recalcitrant soils on surfaces to improve cleaning and hygiene regimes.     

Dust mediated transfer of phosphorus to alpine lake ecosystems of the Wind River Range,Wyoming, USA

Alpine lakes receive a large fraction of their nutrients from atmospheric sources and are consequently sensitive to variations in both the amount and chemistry of atmospheric deposition. In this study we explored the spatial changes in lake water chemistry and biology along a gradient of dust deposition in the Wind River Range, Wyoming. Regional differences were explored using the variation in bulk deposition, lake water, sediment, and bedrock geochemistry and catchment characteristics. Dust deposition rates in the Southwestern region averaged 3.34 g m^?2 year^?1, approximately three times higher than deposition rates in the Northwestern region (average 1.06 g m^?2 year^?1). Dust-P deposition rates ranged from 87 µg P m² day^?1 in the Northwestern region to 276 µg P m² day^?1 in the Southwestern region. Subalpine and alpine lakes in the Southwestern region had greater total phosphorus (TP) concentrations (5–13 µg L^?1) and greater sediment phosphorus (SP) concentrations (2–5 mg g^?1) than similar lakes elsewhere in the region (1–8 µg L^?1 TP, 0.5–2 mg g^?1 SP). Lake phosphorus concentrations were related to dissolved organic carbon (DOC) across vegetation gradients, but related to the percent of bare rock, catchment area to lake area, and catchment steepness across dust deposition gradients. Modern phytoplankton and zooplankton biomasses were two orders of magnitude greater in the Southwest than in the Northwest, and alpine lakes in the Southwest had a unique diatom species assemblage with relatively higher concentrations of Asterionella formosa, Pseudostaurosira pseudoconstruens, and Pseudostaurosira brevistriata. These results suggests that catchment controls on P export to lakes (i.e. DOC) are overridden in dominantly bare rock basins where poor soils cannot effectively retain dust deposited P.     

Distribution characteristics,sources, and ecological risk assessment of polycyclic aromatic hydrocarbons in sediments from Haizhou Bay,China

Sixteen USEPA priority polycyclic aromatic hydrocarbons (PAHs) were analyzed by gas chromatography–mass spectrometry. Twenty samples were collected from the surface sediments of Haizhou Bay in this survey. This research aimed to identify the PAHs' contamination level, composition pattern, pollution sources, and assess the ecological risk of PAHs. The results showed that the sum of PAH concentrations ranged from 116.6 ng g^?1 to 2414.9 ng g^?1 (mean: 662.42 ng g^?1), which is higher than the reported values for different wetlands worldwide. Three- and four-ring PAHs (accounts for more than 70% of the total PAH content) were predominant in the wetland sediment. The PAHs source distribution in the surface sediments were determined using diagnostic ratio and PCA/MLR. Consequently, multiple PAHs sources were found. Of the total PAH, 79.25% was derived from vehicular emission, 20.75% from coal combustion. The effect range low/effect range median (ERL/ERM) values indicated a low toxicity risk level. However, the fluoranthene concentrations exceeded the ERL level, and even the ERM level, in some stations. The mean effects range–median quotient (M-ERM-Q) suggests a low ecological risk for the PAHs in the sediments.     

赣江流域底泥中有机氯农药残留特征及空间分布

基于"临水垂直插管法"采集赣江流域32个采样点的底泥样品,经索氏提取方法(Soxhlet Extraction,SE)前处理及气相色谱法(GC-ECD)检测样品中有机氯农药(OCPs)含量。结合多元统计学和ArcGIS9.3,研究了8种有机氯农药的残留状况及空间分布情况。结果表明,所检测8种OCPs中,除β-HCH有2个点未检出,其它7种OCPs检出率为100%。以DDTs残留含量最高,DDTs平均值为10.40μg/kg,其异构体以p,p’-DDT为主;HCHs的平均值为8.24μg/kg,其异构体以β-HCH为主。它们除了来自环境中的早期残留外,仍然具有新的外源HCHs和DDTs的输入。不同OCPs在研究区分布存在很大差异,HCHs总量分布较高的地区位于流域的中下游,DDTs总量分布较高的地区位于流域的中上游。     

Assessment of the Genotoxic Potential of Sediments Contaminated with POPs and Agricultural Soils Using Vicia faba Micronucleus Assay

The aim of this study was to assess the levels of some persistent organic pollutants in the surface sediments from the Zahuapan and Atoyac rivers (Tlaxcala, Mexico), as well as to determine the genotoxic potential, by the micronucleus test in Vicia faba, of the sediments and agricultural soils irrigated with water from these rivers. This document is the first study on the presence of POPs in surface sediments of the above-mentioned rivers; among the compounds analyzed are the HCH isomers, DDT and its metabolite DDE, HCB, mirex, aldrin, and 41 PCB congeners. The concentrations of HCB, ΣDDTs, ΣHCHs, and ΣPCBs ranged from 138–510, 45–450, 3–27, and 59–1876 μg kg^?1 dry weight, respectively. The highest levels of HCB, HCH isomers, and PCB congeners were found in the Atoyac River, and these compounds have the potential for causing an environmental impact. On the other hand, biological testing shows that both sediments and agricultural soils possess a genotoxic potential, given that the micronuclei frequency in V. faba is increased.     

Boron induced changes in biochemical constituents,enzymatic activities,and growth performance of wheat

The present study investigates how excess boron (B) affects and alters the biochemical constituents and enzymatic activities of wheat (Triticum aestivum var. ‘Raj 4037’), consequently leading to reduced plant growth and yield. Plants were raised in soils supplemented with various concentrations of B (0, 1, 2, 4, 8, 16, and 32 µg B g^?1 soil). Biochemical constituents including soluble leaf protein contents, total phenol contents, soluble sugar contents, proline contents, enzymatic activities of peroxidase (POX), and nitrate reductase (NR) were analyzed. In addition, growth parameters namely shoot–root length, shoot–root fresh and dry weight, seed number and seed weight were analyzed to assess the impact of B toxicity. Results indicate that change in biochemical constituents were correlated with B treatments. Boron concentrations beyond 4 µg g^?1 significantly increased soluble leaf protein contents, total phenol contents, soluble sugar contents, and proline contents. The POX activity was found to be positively correlated with B treatments. B significantly affects nitrogen metabolism and nitrate accumulation which is reflected by the downregulation of NR activity at higher B concentrations. B induced changes in physiological parameters of the plant which subsequently led to the reduction in growth, biomass production, and yield attributes. Out of the various concentrations of B, 8 µg g^?1 was moderately toxic while 16 and 32 µg g^?1 generated high toxicity and induced B stress response to confer tolerance in wheat. Further, a possible mechanism of B toxicity response in wheat is suggested.     

Historical deposition behaviors of organochlorine pesticides (OCPs) in the sediments of a shallow eutrophic lake in Eastern China: Roles of the sources and sedimentological conditions

Organochlorine pesticides (OCPs) were quantified in sediments from Lake Chaohu, a shallow eutrophic lake in Eastern China, to investigate their historical deposition behaviors and to reconstruct their use history. The OCP concentrations ranged from 2.17 to 18.61 ng g⁻¹ in the surface sediments in the lake region and from .28 to 86.27 ng g⁻¹ in the inflowing river. The highest values of the aforementioned variables were attributed to urban-industrial pollution sources in the west lake region and decreased with distance from the river inlets. Historically, OCP contamination displayed three stages in Lake Chaohu: an initial increase before the 1930s, a sharp increase until the 1980s, and a decrease due the implementation of policies banning their use in the 1980s. During the second stage, the OCP concentrations increased rapidly from .69, .58, 1.95 and .02 ng g⁻¹ in the C4, C5, C6 and C10 samples in the 1930s to 8.68, 61.89, 24.14 and 3.53 ng g⁻¹, respectively, in the early 1980s. This temporal trend of OCP concentrations corresponded with historically intense anthropogenic activities, indicating that contamination by OCPs was accompanied by industrialization and civilization prior to their prohibition. In addition, dichlorodiphenyltrichloroethane (DDT) contamination was derived from the historical use of technical DDTs, whereas hexachlorocyclohexane (BHC) contamination was attributed to the historical use of technical BHCs with Lindane and new inputs of illegal DDTs. Strong positive relationships between the OCP concentrations and the total organic carbon (TOC) concentrations, sediment grain sizes (<4 μm), nutrient contents and heavy metal contents indicated that the sedimentary conditions and human activities affected the depositional characteristics of the OCPs. The DDT residues and their metabolites, particularly those in the inlet rivers, should be of concern because they result in an ecotoxicological risk in the catchment of Lake Chaohu.     

Distribution of surface soil mercury of Wuda old mining area,Inner Mongolia,China

In this study, mercury (Hg) concentrations in dustfall and topsoil were investigated. Three hundred forty-four samples were collected, including dustfall and topsoil samples, across an area of ～180 km² in Wuda, China. Dustfall Hg concentration in Wuda ranged from 10 to 6453 ng·g^?1_, with an average of 305 ng·g^?1, and topsoil Hg concentration ranged from 3 to 1537 ng·g^?1, with an average value of 135 ng·g^?1. The average dustfall Hg concentrations in the coalfield, industrial park, and urban areas were 289 ng·g^?1, 809 ng·g^?1, and 160 ng·g^?1, respectively, and the corresponding average topsoil Hg concentrations were 216 ng·g^?1, 242 ng·g^?1, and 91 ng·g^?1. Hg concentrations were significantly higher in the coalfield, industrial park, and urban areas compared with background values for Wuda and China tide soil. The coal Hg concentrations ranged from 273 to 346 ng·g^?1, with an average value of 317 ng·g^?1. Comparison of the Hg concentrations of Wuda coal with other regions and countries, indicated that Hg concentrations were significantly enriched in coal, highlighting that coal is the primary Hg source for Wuda District. While coal fires provided the primary source of Hg, some higher Hg values were caused by factors such as gangue hills and coalfield topography, the use of activated carbon with HgCl₂ as a catalyst in the industrial park, and several coal washeries in wasteland areas. In addition to atmospheric Hg, underground coal seam emissions served as another potential Hg source in the coalfield. The surface soil Hg in the coalfield and industrial park areas should be given closer attention in the future.     

Elevated Concentrations of Pesticides and PCBs in Soils at the Southern Caspian Sea (Iran) are Related to Land Use

Soil contamination by organochlorine pesticides or PCBs is almost undocumented for Iran. Here we report a soil survey in Mazandaran and Guilan provinces that hold >30% of the agricultural areas of Iran where pesticide use is widespread. Concentration of DDTs, HCHs, cyclodienes, and PCBs were measured in 45 soil samples from different agricultural land uses and forest land. The average concentrations of ∑DDT (37 μg kg^?1) and ∑HCH (21 μg kg^?1) in agricultural soils are among the largest ever reported and exceed international soil screening standards. All residues were larger in agricultural than in forest soil. Within agricultural land, ∑DDT were largest for tea gardens, lindane was largest in rice fields, and cyclodiens largest in citrus orchards. The ratio of (DDD + DDE)/DDT is an index of the extent of DDT degradation in soil and was lower in tea gardens than in other soils (0.7 versus 2–5), indicating either ongoing DDT input or lower degradation rate in the tea gardens that are more acid than the other soils (pH 4.5 versus 6.5–7.0). The o,p′–DDT/p,p′–DDT ratio was about 3 in forest soils, suggesting that DDT is derived from dicofol application and not from technical DDT as in agricultural soils. The PCB 28, 180, and 138 showed the highest mean concentration compared with other PCB congeners in all land uses. This survey is the first of this kind for Iran and illustrates that concentrations of organochlorine pesticide in soil are relatively large.