Pollution and Ecological Risk Assessment of Heavy Metals in Farmland Soils in Yanqi County,Xinjiang, Northwest China

A total of 50 farmland soil samples were collected from the Yanqi County, Xinjiang, China, and the concentrations of eight heavy metal elements (As, Cd, Cr, Cu, Mn, Ni, Pb and Zn) were determined by standard methods. The spatial distribution, pollution level and ecological risk status of heavy metals were analyzed based on GIS technology, the Geo-accumulation Index (Igeo), the Pollution Load Index (PLI) and the Potential Ecological Risk Index (RI). Results indicated that: (1) The average contents of Cd, Cr, Ni, Pb, and Zn of farmland soils exceeded the background values of irrigation soils in Xinjiang by 1.5, 1.40, 1.33, 2.63, and 4.92 times, respectively. Cd showed a no-pollution level, Zn showed a partially moderate pollution level, Pb showed a slight pollution level, and Cr, Cu, As, Mn, and Ni showed no-pollution level, compared to the classification standard. The PLI values of heavy metal elements of farmland soils varied from 0.83 to 1.89, with an average value of 1.29, at the moderate pollution level. (2) The Individual Potential Ecological Risk Index for heavy metals in the study area was ranked in the order of: As > Ni > Cu > Cd > Pb > Cr> Zn. The RI values of heavy metals of farmland soils varied from 3.45 to 11.34, with an average value of 6.13, at the low ecological risk level. (3) Cu and Mn of farmland soils were mainly originated from the soil parent material and topography of the study area. As, Cd, Ni and Pb were mainly originated from human activities, and Cr and Zn may originated from both natural and anthropogenic factors in the study area.     

博斯腾湖湿地边缘带农田土壤重金属的污染风险评价

对新疆博斯腾湖湿地边缘带农田土壤中8种重金属元素(As、Cd、Cr、Cu、Mn、Ni、Pb和Zn)地球化学特征进行分析。采用污染负荷指数(PLI)、潜在生态风险指数(RI)和生态风险预警指数(IER)对农田土壤重金属污染与环境风险进行评价。结果表明:(1)湿地边缘带农田土壤Pb和Zn呈现重度污染,As、Cd、Cr和Ni轻度污染,Cu轻微污染,Mn无污染。土壤As、Cd、Cr、Cu、Ni、Pb和Zn平均含量处于轻微风险水平。Cd是污染程度与生态风险等级最高的重金属元素;(2)湿地边缘带农田土壤PLI平均值为1.43,呈现轻度污染,RI平均值为20.62,呈现轻微生态风险状态,IER的平均值为–4.53,呈现无警态势。湿地边缘带PLI、RI与IER空间分布格局基本一致;(3)湿地边缘带农田土壤Pb与Zn来源主要受到人类活动的影响,Cr、Cu、Mn与Ni来源主要受到土壤地球化学作用的控制,As与Cd受自然因素和人为因素共同影响。     

Retention Capacity and Environmental Mobility of Pb in Soils along Highway Corridor

Although lead (Pb) emissions have dropped drastically with the phase-out of tetra-ethyl lead (TEL) as a fuel additive, Pb deposited along highway corridors continues to be of concern because of its toxicity. This paper provides comprehensive data on the extent and distribution of Pb in roadside soils, Pb interaction with soils as a function of soil composition, the retention capacity of soil based on batch adsorption tests, the retention mechanism of Pb using selective sequential extraction, the potential for mobility using batch desorption tests with simulated rain and winter road salt, and column leach tests. Highway soils on high-traffic sections near Burnaby, Canada were found to have Pb accumulations up to 1628mg/kg soil. Contamination was mainly in the top 0.3m, with concentrations rapidly decreasing to the background level at a depth of 0.6m. The top layer contained more organic material and had a high adsorption capacity. Highway soils were found to have 3–10 times higher Pb adsorption capacities than the amount currently deposited. Selective sequential extraction indicated low exchangeable Pb in highway soils. Batch desorption tests with leaching solutions of H₂O (pH 5.5), HNO₃ solution (pH 4.0) and aqueous NaCl solution (0.17M) indicate low likelihood of significant leaching. Selective sequential extraction, leachate extraction and desorption tests show that Pb has limited mobility in highway soil.     

苦水玫瑰产地土壤重金属污染评价与溯源解析

探明特色农产品产地土壤重金属污染特征及其污染来源可促进特色农作物产业的健康有序发展,对于助力乡村振兴和发展乡村特色产业具有重要意义。该研究以苦水玫瑰产地土壤为研究对象,应用内梅罗综合污染指数法、污染负荷指数法和改进物元可拓模型来量化土壤重金属As、Cd、Cr、Cu、Hg、Ni、Pb和Zn的污染水平并进行对比分析,还利用正定因子矩阵模型(positive matrix factorization, PMF)进行土壤重金属溯源解析。结果表明:1)研究区土壤除Hg和Cr的均值低于兰州市和甘肃省土壤背景值之外,其余As、Cd、Cu、Ni、Pb和Zn的均值都高于二者的背景值,但所有元素的测定值均低于《土壤环境质量农用地土壤污染风险管控标准(试行)(GB 15 618-2018)》(pH值大于7.5)的筛选值。2)内梅罗综合污染指数和污染负荷指数分别处于0.71～2.02和0.64～1.48之间,均值为1.41和1.17,土壤总体上为轻度污染。改进物元可拓模型评价结果显示研究区土壤总体上处于尚清洁状态,与内梅罗综合污染指数与污染负荷指数评价结果基本一致,但改进物元可拓模型的评价结果更具有实际指导意...     

模拟酸雨对太湖地区水稻土铜吸附—解吸的影响

以太湖地区三种典型的水稻土（黄泥土、白土、乌泥土）为例，利用模拟-培养试验，着重研究模拟酸雨对土壤的铜吸附解吸能力的影响，研究结果表明：与未淋溶土壤相比，经模拟酸雨淋溶的三种土壤对铜的吸附量有所增加，随着淋溶液pH的降低，增幅减小：易解吸态铜的解吸量则随淋溶液pH的降低而增大，模拟酸雨降低了土壤对重金融污染的缓冲能力；虽然黄泥土、乌泥土对铜的吸附量远大于白土，但模拟酸雨对乌泥土的吸附-解吸能力的影响速度也大于白土。     

Fraktionen und löslichkeit der schwermetalle Cd,Co, Cr,Cu, Ni und Pb im Boden

A successive fractionation of heavy metals — Cd, Co, Cr, Cu, Ni and Pb — as water soluble, 0.01 N NH₄Cl-exchangeable and 0.01 N NaOH-extratable was carried out, in order to determine their chemical forms in soils. Ionic activities of the heavy-metal compounds expected in equilibrium soil solutions were calculated and are presented in a solubility diagram as a function of pH.The ionic activities in soil solutions show an undersaturation with respect to heavy metal-oxide, -carbonate, -sulfate, -chloride and -phosphate compounds. The ionic activities of the elements studied are pH dependent; the correlation coefficient for pH vs pCd reaches a value 0.66 (significant at the 1 % level). Significant correlations between ionic activities and NH₄-Cl-exchangeable fractions were found for Cd, Co, Ni and Pb with correlation coefficient values of 0.88, 0.89, 0.97 and 0.79, respectively. It can therefore be assumed that desorption and adsorption phenomena are responsible for the regulation of heavy-metal behaviour in soils. The NaOH-extractable fraction of the heavy metals studied does not show any relationship to the organic matter in the soils.     

外源硅对不同pH水田土壤铅吸附热力学特征的影响

通过等温吸附试验,研究外源硅对两种不同pH水田土壤铅吸附热力学特征的影响。试验中采用硝酸中和硅酸钠的碱性,以硝酸钠补齐各处理间钠离子和硝酸根离子的差异,消除了因加入硅酸盐改变体系pH及伴随离子对土壤吸附铅可能产生的影响。结果表明：在本试验中,Freundlich方程能较好地描述3种温度下两种土壤对铅的吸附特征;加硅促进了酸性土壤对铅的吸附,抑制了碱性土壤对铅的吸附;根据热力学函数关系计算的△G〈0、△H〉0、△S〉0,说明两土壤对铅的吸附是吸热、熵增的物理过程为主;加硅后,酸性土壤△G变小、△H变大、△S变大,碱性土壤△G变大、△H变小、△S变小,说明加硅使酸性土壤吸附铅的自发性提高、碱性土壤吸附铅的自发性降低。     

珠三角滩涂围垦农田土壤和农作物重金属污染

为了研究珠三角滩涂围垦农田土壤和农作物重金属污染状况,采集了广州南沙、中山一带围垦农田农作物及其根际土壤样品,测定重金属的质量分数。结果表明,围垦农田土壤样品中Cu、Ph、Cd、Ni、Cr和Zn含量均大于广东省相应土壤环境背景值,其中Cu（56．06mg·kg^-1）、Pb（48．30mg·kg^-1）、Cd（0．72mg·kg^-1）、Ni（41．15mg·kg^-1）、Cr（115．1mg·kg^-1）和Zn（200．1mg·kg^-1）分别为背景值的3．30、1．34、12．82、2．26、2．28和4．23倍。与《土壤环境质量标准》（GB15618-1995）中Ⅱ级标准（pH〈6．5）比较,土壤样品中Cu、Cd、Ni和Zn的超标率分别为73．7％、88．6％、59．6％和28．9％。以GB15618-1995中Ⅱ级标准为评价标准,采用Nemerow指数法进行评价,土壤重金属平均综合污染指数为1．86,属3级轻污染。与《食品中污染物限量》（GB2762-2005）等相关标准比较,农作物中Cu、Pb、Cd、Ni、Cr和Zn含量的样品超标率分别为0、28．9％、2．6％、48．3％、12．3％和6．1％。由此可见,珠三角滩涂围垦农田土壤和农作物重金属污染问题已经比较突出,土壤污染以Cd为主,而农作物污染则以Ni、Ph、Cr为主。     

Adsorption and Desorption of Copper in Pasture Soils

Abstract

Copper (Cu) is bound strongly to organic matter, oxides of iron (Fe) and manganese (Mn), and clay minerals in soils. To investigate the relative contribution of different soil components in the sorption of Cu, sorption was measured after the removal of various other soil components; organic matter and aluminum (Al) and Fe oxides are important in Cu adsorption. Both adsorption and desorption of Cu at various pH values were also measured by using diverse pasture soils. The differences in the sorption of Cu between the soils are attributed to the differences in the chemical characteristics of the soils. Copper sorption, as measured by the Freundlich equation sorption constants [potassium (K) and nitrogen (N)], was strongly correlated with soil properties, such as silt content, organic carbon, and soil pH. The relative importance of organic matter and oxides on Cu adsorption decreased and increased, respectively, with increasing solution Cu concentrations. In all soils, Cu sorption increased with increasing pH, but the solution Cu concentration decreased with increasing soil pH. The cumulative amounts of native and added soil Cu desorbed from two contrasting soils (Manawatu and Ngamoka) during desorption periods showed that the differences in the desorbability of Cu were a result of differences in the physico‐chemical properties of the soil matrix. This finding suggests that soil organic matter complexes of Cu added through fertilizer, resulted in decreased desorption. The proportions of added Cu desorbed during 10 desorption periods were low, ranging from 2.5% in the 24‐h to 6% in the 2‐h desorption periods. The desorption of Cu decreased with increasing soil pH. The irreversible retention of Cu might be the result of complex formation with Cu at high pH.     

阴离子对加入到土壤中的铅吸附与提取的影响

The effect of accompanying anions on the adsorbability and extractability of Pb added in soils was studied by using bach equilibria and incubation-extraction mothods.Pb concentration ranged between 0.48-2.41 mM in the adsorption experiment,and Pb added to soil from 2.14 to 19.31mM Pb/kg with an incubation time of 2-16 weeks in the incubation-extraction test in which 1M NH4OAc(pH 7) was taken as an extraction agent,and the Pb compounds used are PbCl2,Pb(NO3)2 and Pb(OAc)2.The values of pH50 for Pb retention and the parameters,b and k values,of Langmuir equation were used to distinguish the difference of adsorbability and extractability of Pb affected by anions,respectively.Judging from the results of either pH50 value or b value,the influences of Cl^- and NO3^- on the adsorbability and extractability of Pb in soils were similar but quite different from those of OAc^-.The relative loading capacities of soils to Pb calculated according to the extraction rate showed that the values of Pb(OAc)2 were higher than those of PbCl2 and Pb(NO3)2.     

Acetochlor as a soil pollutant

The agricultural use of pesticides leads to diffuse pollution whereby the various contaminants of the soil infiltrate into the groundwater reaching lakes and drinking water aquifers. Due to the extensive application of these chemicals, their leaching presents a high environmental risk. Since the adsorption coefficient (K) characterizes the soil / water partitioning [1] and is also representative for leaching, the first step in understanding of the environmental fate of a pollutant is to study its adsorption properties. Weak binding to the soil constituents (low K) leads to groundwater pollution, while a strong binding (high K) results in surface water pollution through the erosion of the soil. Acetochlor is a widely used herbicide all over the world. Similar to other organic pollutants, the environmental fate of this chemical is strongly related to its adsorption properties. Static adsorption equilibrium measurements were carried out at 25°C on different types of Hungarian soils (chernozem, brown forest and sandy soil) characterized by varying amounts of organic matter and pH values. Acetochlor solutions were prepared in the presence of nitrate and phosphate ions (0.1 mol/L sodium nitrate and 0.1 mol/L phosphate uffer, pH=7) which are constituents of fertilizers occurring in high concentrations in the environment. In order to appreciate their effect, adsorption studies were also performed in pure aqueous medium. The equilibrated liquid was analyzed after centrifugation by two different methods (Total Organic Carbon measurement, High Performance Liquid Chromatography). Isotherms obtained under different conditions, as well as on various soils, exhibit a similar shape, thus indicating a two-step adsorption process. The plots cannot be interpreted according to the classes of isotherms suggested by Giles (H-, L- and C-type, [2]). The adsorption coefficients were estimated from the initial slope of the curves. These values were determined not only by the type of the soil, but also by the composition of the aqueous media. Due to the low value of the adsorption coefficients, the acetochlor is a rather mobile pollutant of the soil posing a potential danger to the aquatic environment. The organic matter adsorption coefficients (K_om) [3] were also calculated and they were approximately identical for soils of high organic matter. For the chernozem and brown forest soils, the values of the K and K_om parameters are increasing in the order from water < phosphate buffer < sodium nitrate. For soils of low organic content, the similarity of the K_om values cannot be expected (due to the hyperbolic nature of the equation) as the data really indicate it for the adsorption behavior of the sandy soil. Here, the organic matter plays a less important role and the adsorption is controlled by the solute / inorganic substance interactions. This conclusion is nicely proved by the adsorption of the acetochlor on quartz resulting thereby in a similar plot being obtained for the soils. According to the hypothesis presented here, the first step of the isotherms is controlled by the solute / surface interactions while the solute / adsorbed solute interactions are operating in the second step of the isotherm. The role of the organic matter in this region of the isotherm is probably negligible. The comparison of the adsorption coefficients leads to the conclusion that the presence of nitrate and phosphate ions enhances the adsorption of acetochlor on the soils containing a high percentage of organic matter. As these ions are present in the environment due to the extensive use of fertilizers, they may increase the acetochlor pollution of water by erosion. This conclusion corroborates those earlier observations that reported frequent acetochlor contamination of the surface waters [4–5]. As the organic matter content of the soils plays an important role in the acetochlor adsorption, humic substances must have a strong influence on the transport of this compound. Experiments to obtain adsorption isotherms of further pesticides and the development of a quantitative model are in progress.     

污染水稻土中重金属的形态分布及其影响因素

通过BCR3步提取法研究了江西省贵溪铜冶炼厂污染区水稻土中重金属的形态分布。研究表明,废渣场渗滤液污染区域(渣场区)的污染较污水灌溉污染区(污灌区)严重,渣场区土壤中Cu、Pb、Cd的含量高于污灌区,而污灌区土壤Ni含量较高。在表层(0～20cm)水稻土中,Cu以可氧化态为主,Pb以可还原态和可氧化态为主,Cd以酸溶态为主,Ni以残渣态为主,不同重金属元素的有效态所占总量百分比大小顺序是Cd>Cu>Pb>Ni。土壤重金属不同形态之间也呈现一定的相关性,说明Cu与Pb、Cd、Ni之间具有同源性。土壤pH主要影响了污灌区中Cu的形态分布,以及渣场区土壤酸溶态Ni的分布。土壤有机质含量对各重金属形态分布的影响不明显。     

黔产薏苡仁及其产地土壤重金属污染的特征

[目的]探明黔产薏苡仁及其产地土壤重金属污染特征,为黔产薏苡仁产业可持续发展及其产地土壤重金属防控提供科学依据.[方法]以黔西南薏苡仁及其产地土壤为供试样品,分析测定土壤pH值、有机质、阳离子交换量(CEC)和5种重金属元素镉(Cd)、铅(Pb)、锌(Zn)、铜(Cu)、镍(Ni)的含量,运用GIS和单因子污染风险评价...     

支持电解质浓度对磷酸根在可变电荷土壤表面吸附和解吸的影响

研究了离子强度对2种可变电荷土壤中磷酸根吸附和解吸的影响。结果表明,当pH分别大于3.7和4.0时,红壤和砖红壤对磷酸根的吸附量随离子强度的增加而增加;当pH分别小于3.7和4.0时,红壤和砖红壤对磷酸根的吸附量随离子强度呈相反的变化趋势。电解质主要通过改变离子专性吸附面上的电位来影响磷酸根的吸附。Zeta电位的测定结果表明,当pH大于土壤胶体的等电点(IEP)时,吸附面上电位为负值,且随离子强度增加数值减小,对磷酸根的排斥力减小,土壤表面对磷酸根的吸附量增加;当pH小于IEP时,吸附面上的电位为正值,它随离子强度增加而减小,不利于磷酸根的吸附。解吸实验的结果表明,吸附于可变电荷土壤表面的磷酸根在去离子水中的解吸量高于0.1 mol L-1NaNO3体系中的解吸量。这同样由于电解质浓度对土壤表面吸附面上的电位的影响所致。     

辽宁省污灌区土壤重金属污染特征与生态风险评价

针对当前污灌区土壤污染研究中存在的问题,提出了一种模糊识别模型评价土壤综合环境质量,并对潜在生态风险指数法进行改进,用以计量重金属潜在生态风险。采用建立的方法对辽宁省污灌区土壤环境质量和重金属潜在生态风险进行了评价,结果显示:Cd是辽宁省污灌区首要重金属污染物,而Hg、Pb、Ni污染较为普遍;重金属的来源主要是灌溉污水和农田施肥;以工业废水为灌溉用水的灌区污染情况比以河水为灌溉用水的灌区污染严重;污灌区重金属元素污染程度大小依次为:Cd>Pb>Ni>Hg>Cu>Cr>As,而重金属潜在生态风险从大到小则依次为:Cd>Hg>Pb>Cu>Ni>As>Cr。总体来看,辽宁省污灌区存在一定程度的重金属污染,且具有较为明显的复合型污染特点,其潜在生态风险超出警戒水平,各灌区应根据各自污染特点和风险等级制定相应的污染防治对策。     

Adsorption and desorption of imazosulfuron by soil

Understanding and quantifying the adsorption and desorption of herbicides by soil is important for predicting their fate and transport in the environment. Here we report a study concerning the adsorption and desorption, by four different soils, of imazosulfuron, 1-(2-chloroimidazo[1,2-a]pyridin-3-ylsulfonyl)-3-(4, 6-dimethoxypyrimidin-2-yl)urea, a new sulfonylurea herbicide. Both phenomena are well-described by the Freundlich equation, which shows this herbicide to be little adsorbed by each of the four soils investigated. The Freundlich adsorption constants, K(f-ads), ranged from 1.46 to 3.02. Distribution coefficients between soil and water, Kd, measured on soils of different organic matter contents and pH values showed an important effect of these two parameters on imazosulfuron retention. The Freundlich desorption data indicated that a significant amount of the imazosulfuron sorbed is not easily desorbed. The desorption process showed an evident hysteresis phenomenon, which may contribute to the persistence of imazosulfuron in soil.     

四川盆地丘陵区农田土壤对磷的吸附与解吸特征

研究了四川盆地丘陵区典型水田和旱地土壤对磷的吸附与解吸特征,并讨论了吸附-解吸参数与土壤基本理化性质的关系。结果表明,不同pH的农田土壤对磷的吸附和解吸均存在显著差异,土壤对磷的吸持能力表现为中性土壤〉酸性土壤〉石灰性土壤,中性有利于土壤吸附磷;水稻土对磷的最大吸附容量（Qm）和最大缓冲容量（MBC）高于紫色土,而临界平衡磷浓度（EPC0）和解吸率（b）低于紫色土。农田土壤对磷的吸附与解吸参数还受土壤理化性质的影响,Qm和MBC与有机质含量、无定形铁（Fe-ox）含量呈极显著正相关（P〈0.01,n=6）;吸附常数（K）与有机磷含量呈显著负相关（P〈0.05,n=6）;EPC0与土壤pH、CaCO3含量呈显著负相关,与有机磷含量呈显著正相关（P〈0.05,n=6）;b与Fe-ox含量呈显著负相关（P〈0.05,n=6）。     

Quantifying effects of primary parameters on adsorption–desorption of atrazine in soils

Purpose

Adsorption and desorption are important processes that influence the transport, transformation, and bioavailability of atrazine in soils. Equilibrium batch experiments were carried out to investigate the adsorption–desorption characteristics of atrazine. The objectives of this study were to (1) determine and quantify the main soil parameters governing atrazine adsorption and desorption phenomena; (2) find the correlativity between the identified soil parameters; and (3) investigate the universal desorption hysteresis traits.

Materials and methods

Fifteen soils with contrasting physico-chemical characteristics were collected from 11 provinces in eastern China. The equilibrium time was 24 h both for adsorption and desorption experiments. Atrazine was detected by Waters 2695/UV HPLC.

Results and discussion

Adsorption isotherms of atrazine could be well described by the Freundlich equation (r?≥?0.994, p?<?0.01). The total organic carbon (TOC) was the first independent variable that described 53.0 % of the total variability of K _f, followed by the pH (9.9 %), and the clay (4.0 %) and silt (1.2 %) contents, separately; while the primary soil properties that affect desorption parameters included the TOC, pH, free Fe₂O₃ (Fe_d) and the sand content, with the biggest contribution achieved by the TOC (ranged from 48.5–78.1 %). The results showed that when the content ratio of clay to TOC (RCO) was less than 40, the atrazine adsorption was largely influenced by the organic matrix, while when the RCO was greater than 40, they were vital affected by the clay content.

Conclusions

Adsorption–desorption isotherms of atrazine in soils were nonlinear. The content of TOC, clay, and iron oxides, as well as the pH value were the key soil parameters affecting the adsorption–desorption of atrazine in soil, among which the RCO especially exhibited relevance. Additionally, the desorption hysteresis existed for atrazine retention in all 15 tested soils, and the hysteretic effect enhanced with the increasing time for desorption. This would be ascribed to the heterogeneity physical–chemical properties of these soils.     

应用Langmuir等温式解释我国东北某些土壤对磷酸离子的吸附作用

目前应用Langmuir吸附等温式来探讨土壤对磷酸离子的吸附作用,较为广泛.自从Olsen(1957)系统地报道以来,从机理到结合生产实际的研究已有大量的报道,我国近年来也有研究.由于土壤本身组成的复杂性,多数学者用纯物质(如纯粘土或铁与铝的含水氧化物等)进行吸附等温式的机理研究,已取得了很多结果.     

Influence of soil physicochemical and biological properties on the degradation and adsorption of the nematicide fosthiazate

The degradation and adsorption of the organophosphorus nematicide fosthiazate were investigated in nine soils with various physicochemical and biological characteristics. Fosthiazate was more persistent in acidic soils (pH <6), with half-life (t1/2) values ranging from 53.3 to 57.7 days, compared to soils with higher pH (pH >7), with t1/2 ranging from 14.1 to 20.7 days. Application of antibacterial and antifungal antibiotics to soil samples resulted in a significant inhibition of fosthiazate degradation only in two of the three acidic soils. In contrast, soil autoclaving resulted in doubling the t1/2 of fosthiazate in all studied soils, suggesting that both microbial and abiotic processes contribute to fosthiazate degradation. Statistical analysis indicated a significant negative correlation (P < 0.01) between soil pH and t1/2. Fosthiazate was generally weakly adsorbed with Freundlich adsorption coefficient (Kf) values ranging from 1.23 to 2.74 mL/g. Fosthiazate concentration was strongly correlated with soil organic matter content with higher Kf values in soils with higher organic matter content (P < 0.01). The mean t1/2 and Kf values derived from the laboratory studies were used to parametrize the FOCUS groundwater (GW) models PRZM, PELMO, PEARL, and MACRO for nematicide application in potato and tomato crops. Predicted environmental concentrations produced by the models PEARL and MACRO suggested a potential risk for GW in several scenarios, unlike PELMO and PRZM, which predicted low risk for GW. These findings suggest that the environmental fate of fosthiazate is strongly influenced by soil characteristics and that this nematicide should be used with care in acidic, light soils with low organic matter content.