温州城市河流河岸带土壤中PAHs的污染特征与来源

为研究城市河流河岸带土壤中多环芳烃（PAHs）的污染特征,于2010年8月沿温州九山外河和山下河河岸带采集了21个表层土壤样品,利用加速溶剂萃取仪（ASE）萃取,净化柱提取净化,使用气相色谱-质谱联用仪（GC-MS）分析了土壤中18种PAHs的含量.结果表明,温州九山外河和山下河河岸带表层土壤中PAHs含量范围为60.7～3 871.3 ng·g-1,山下河河岸带土壤中ΣPAHs含量显著低于九山外河.两条河流河岸带土壤中的PAHs均以2、3环的低环为主,平均占到PAHs总量的62.47%～72.51%.与国内外其他研究地区土壤中PAHs含量相比,研究河段河岸带土壤中的PAHs处于中等污染水平,但有3个样品中BaP浓度远大于前苏联土壤标准,应引起足够重视.利用Ant/（Ant＋Phe）和Fla/（Fla＋Pyr）比值法和主成分分析方法进行判源,温州城市河流河岸带土壤中的PAHs均表现出明显的燃烧源和石油源的综合来源特征。     

电子废物拆解区农业土壤中PCNs的污染水平、分布特征与来源解析

用GC-NCI-MS法测定了路桥农业表层土壤中46种多氯萘(PCNs)的含量.目的是了解该地区表层土壤中PCNs的污染水平、空间分布特征和来源.结果表明,所有表层土壤样品中ΣPCNs的含量为0.062～2.92 ng.g-1,平均值为0.630 ng.g-1.多数样品中tetra-CNs和penta-CNs是最主要的同族体,分别占18.4%～88.8%(平均值为46.7%)和8.40%～53.1%(平均值为30.7%),其次是tri-CNs,范围为0～47.3%,平均值为10.6%.聚类分析和燃烧指示物分析表明,采样点主要受Halowax1014和Halowax 1013工业品污染,PCBs工业品和电子废物燃烧也可能对污染有贡献.与国内外其它研究相比,研究区域内土壤中PCNs污染处于中等水平.     

Evaluation of the European Space Agency Climate Change Initiative Soil Moisture Product over China Using Variance Reduction Factor

In this study, we evaluated the European Space Agency Climate Change Initiative soil moisture product v02.1 (ESA CCI SM v02.1) using in situ observations collected at 547 stations in China from 1991 to 2013. A conventional validation was first conducted, and the triple collocation errors of ESA CCI SM and the European Centre for Medium Range Weather Forecasting reanalysis data were approximately 0.053 and 0.050 m³/m³, respectively. To obtain more reliable validation results, the average soil moisture of the in situ observations per ESA CCI SM pixel was also used as the validation sites. Variance reduction factor (VRF) was adopted to quantify the accuracy of the soil moisture validation sites, and the average VRF was estimated at 4.88%. The validation results were enhanced by excluding validation sites with VRF errors greater than 5% from the statistical analysis. Although the ESA CCI SM underestimated the in situ observations with a Bias of 0.05 m³/m³, a moderately high correlation coefficient of 0.44 and a relatively small unbiased root‐mean‐square difference of 0.05 m³/m³ were observed. This study provides information on the utilization of ESA CCI SM for ecological protection, climate change, and hydrological forecasting. It also suggests the adoption of VRF for future error corrections of satellite‐based products.     

乌梁素海周围盐化潮土钠质化特征

以乌梁素海周围盐角草(CSE)、碱蓬(CSG)、盐爪爪(CKF)和苦豆子(CSA)群落的盐化潮土为研究对象,分别采集0～20,>20～40,>40～60和>60～80 cm共16个混合土样. 测定土壤pH,含水量,含盐量,钠吸附比(SAR)和交换性钠离子百分率(ESP)等指标,分析了土壤的碱化特征. 结果表明:CSE土壤剖面含盐量,SAR和ESP的平均值最高,其次为CSG,CKF和CSA土壤. CSE土壤金属离子总量最大,其次为CSG,CKF和CSA;阳离子以Ca2+和Na+为主,阴离子以Cl-和SO2-₄为主,而CO₃2-和HCO₃-含量极低. 土壤盐分主要以氯化物和硫酸盐为主,碳酸盐以碳酸钙形式存在. ESP与含盐量(R20.834,P0.000 8)和SAR(R20.862,P0.000 2)之间均呈现显著的正相关,ESP随着含盐量和SAR的增大而增大,SAR可以替代ESP的测量. 土壤剖面盐分的分布状况是在降水、蒸发、灌溉和地下水等因素的综合作用下形成的.      

水稻土中氮素对微生物固砷的扰动及效应机制

我国是世界上最大的水稻生产国,水稻生产在粮食安全方面起着重要的作用.现阶段,我国稻田土壤的砷污染问题表现突出.稻田长期处于淹水的缺氧环境下,微生物在厌氧条件下介导的砷形态转化速率和程度均强于化学过程.理解和认知微生物对稻田土壤中砷固定的关键过程及作用机制将为开展稻田砷污染的有效治理提供理论依据.在综合分析了砷在稻田土壤中的迁移及其影响因素的基础上,主要综述了涉及淹水稻田土壤中微生物参与As （Ⅲ）固定两条重要途径：Fe （Ⅱ）氧化成矿耦合As （Ⅲ）固定（间接过程）与As （Ⅲ）直接氧化固定（直接过程）.同时,就氮素在土壤的形态及分配对微生物参与砷固定的响应过程也展开系统性论述.其中,总结了参与微生物砷固定与氮素转化的关键基因表达及代谢机制;最后,归纳了砷污染稻田微生物修复技术的相关研究进展,并提出了初步展望.     

Adsorption–desorption behavior of atrazine on agricultural soils in China

Adsorptionanddesorptionareimportantprocessesthataffectatrazinetransport,transformation,andbioavailabilityinsoils.Inthisstudy,theadsorption–desorptioncharacteristicsofatrazinein three soils (laterite, paddy soil and alluvial soil) were evaluated using the batch equilibrium method. The results showed that the kinetics of atrazine in soils was completed in two steps: a “fast” adsorption and a “slow” adsorption and could be well described by pseudo-second-order model.In addition,the adsorption equilibrium isotherms were nonlinear and were well fitted by Freundlich and Langmuir models. It was found that the adsorption data on laterite, and paddy soil were better fitted by the Freundlich model;as for alluvial soil,the Langmuir model described it better. The maximum atrazine sorption capacities ranked as follows: paddy soil > alluvial soil > laterite. Results of thermodynamic calculations indicated that atrazine adsorption on three tested soils was spontaneous and endothermic. The desorption data showed that negative hysteresis occurred. Furthermore, lower solution pH value was conducive to the adsorptionofatrazineinsoils.Theatrazineadsorptioninthesethreetestedsoilswascontrolled by physical adsorption, including partition and surface adsorption. At lower equilibrium concentration, the atrazine adsorption process in soils was dominated by surface adsorption;while with the increase of equilibrium concentration, partition was predominant.     

悬浮液进样FAAS法测定黄棕壤中的微量铜

本文采用悬浮进样火焰原子吸收光谱法测定黄棕壤中微量铜 ,并对样品的研磨时间、悬浮液浓度、酸度选择及校正方法等进行了探讨。实验表明 :该法的检出限 (K =3)为 0 .12μg· g-1,精密度 (RSD)为4.6 % ,加标回收率为 98～ 10 6 % ,对水系沉积物 GSD5、GSD6标准样品测定结果与推荐值吻合。     

Occurrence and congeners specific of polychlorinated biphenyls in agricultural soils from Southern Jiangsu, China

A total of 198 agricultural soil samples were collected from Zhangjiagang and Changshu in Southern Jiangsu for analysis of 13 polychlorinated biphenyls （PCBs） in order to assess the levels of pollution, sources, area distribution, and potential risk for the environment. All methods were rigorously tested and an adequate quality control was ensured. Only one site had no PCBs residues, and the highest total PCBs concentration in the surface soils was 32.83 ng/g. The average concentration in all the soil samples was 4.13 ng/g, signaling low-level pollution. Tetra-, penta-, and hexa-chlorinated biphenyls were dominant species in soil samples, accounting for more than 75% of ∑PCBs in the soil samples. PCB118 was the most abundant congener in all the samples. The PCB118 was about 20% of ∑PCBs. The soil organic matter content showed only a weak correlation with the levels of all PCB congeners, in which a better correlation was noted for the more volatile lighter PCB congeners than for the heavier homologues. To a certain extent, the sources and land use seemed to influence the levels of PCBs.     

广州地区农田土壤中有机氯农药残留分布特征

以网格法在农田土壤中均匀布点,采集土壤样品75个,对广州地区农田土壤中有机氯农药含量及分布状况进行了研究。结果表明,试区土壤有机氯农药的检出率为100％,表明广州地区农田土壤中有机氯农药残留现象普遍存在。六六六（HCHs）和滴滴涕（DDTs）的平均含量分别为42．75μg/kg、52．76μg/kg,含量范围分别在1．35—803．72和2．73—1036．90μg/kg。与国内不同区域的同类研究相比,广州地区土壤的有机氯残留水平较高。在不同利用类型土壤中,有机氯残留状况有所差异,六六六在水稻土中残留量最高,而滴滴涕在菜园土中含量最高。     

上海崇明岛蔬菜地土壤重金属含量与生态风险预警评估

崇明3城镇蔬菜地土壤重金属的总体含量为Cu 29.2 mg·kg^-1、Pb 26.5 mg·kg^-1、Cr 79.4 mg·kg^-1、Zn 91.2 mg·kg^-1和Cd 0.222 mg·kg^-1.除Cd在城桥镇和陈家镇超过国家土壤一级标准(GB 15618-1995)外,其余均低于国家土壤一级标准,并且满足国家对绿色食品产地土壤重金属含量的要求(NY/T391-2000).与上海土壤背景值相比,Cu、Pb、Cr、Zn和Cd分别高出上海土壤背景值 24.3％、24.4％、22.9％、18.8％和65.7％.崇明3城镇蔬菜地土壤重金属生态风险预警评估得出,23个采样点中有3个样点属于中警,10个样点属于轻警,8个样点属于预警,1个样点属于无警,综合评估I_{ER＝1.562,为轻警.3城镇生态风险排序为堡镇（IER=1.799）>城桥镇（IER=1.636）>陈家镇（IER=1.368）,均属于轻警.}