混合嗜酸菌浸出污泥中重金属机制判定方法

为判断混合菌种的生物沥浸机制,采用添加沥浸混合菌种+作用底物（硫酸亚铁铵、硫粉）、只添加作用底物和仅加硫酸3组实验,估算直接氧化作用（F₁₁）,化学氧化作用（F₁₂）和酸性浸出作用（F₁₃）的贡献率,从而获得混合菌种的重金属浸出机制.针对某污水处理厂剩余污泥的生物沥滤实验结果表明,Cu的浸出过程中F₁₁、F₁₂、F₁₃贡献率分别为92.55%、7.45%、0%,说明混合菌种作用下Cu的浸出机制主要为直接机制;Zn的沥浸作用中F₁₁、F₁₂、F₁₃贡献率分别为18.86%、44.35%、36.79%,判定Zn在混合菌种的作用下为间接机制.该法可在实际环境条件下判定重金属的生物沥浸机制,对相关研究和实际应用提供理论依据.     

起爆药污染场地土壤中锑的环境风险评估

为研究起爆药污染场地土壤中Sb（锑）的环境风险,利用微波消解原子荧光光度法、Tessier逐级提取法、TCLP（toxicity characteristic leaching procedure）毒性浸出法及SBET（simplied bioaccessibility extraction test）方法,分析了某起爆药场地表层土壤中Sb的价态、形态、浸出水平和生物可给性及其对人体健康风险水平和地下水环境风险水平的影响.结果表明:①土壤中w（TSb）为26.7~4 255.0 mg/kg,是GB 36600-2018《土壤环境质量建设用地土壤污染风险管控标准》中第一类用地筛选值的1.33~212.75倍,最大值超过相应管制值的10.82倍.土壤样品中Sb主要以Sb5+存在,w（Sb5+）在w（TSb）中的占比达65.57%~95.46%.②土壤中不同形态Sb的比例由高到低依次为残渣态（38.05%~94.22%）、铁锰氧化物结合态（0.01%~31.80%）、有机结合态（0.32%~21.55%）、碳酸盐结合态（0.01%~11.16%）和可交换态（0.42%~3.70%）.土壤中w（可交换态Sb）与CEC（阳离子交换量）呈负相关,w（铁锰氧化物结合态Sb）与w（Fe）、w（Mn）均呈正相关.③土壤中Sb的浸出浓度为0.22~35.49 μg/L,并随土壤中w（砂粒）、w（TSb）、w（碳酸盐结合态Sb）和w（可交换态Sb）的增大而升高,随CEC的增大而降低.④土壤中Sb的生物可给性范围在8.03%~67.69%之间,w（Fe）和w（OM）的增加能够降低Sb的生物可给性.⑤基于Sb生物可给性健康风险水平和基于Sb价态健康风险水平的结果分别是以w（TSb）为暴露浓度计算的传统风险评估模型预测结果的8.00%~67.69%和62.00%~77.01%,土壤中Sb的实际浸出浓度较常规模型（三相平衡耦合地下水稀释模型）预测值低3~5个数量级.研究显示,充分考虑Sb在起爆药污染场地土壤中的赋存特征能够降低常规风险评估方法的保守性.      

Behaviour and mobility of preemergent herbicides in turfgrass: A field study

Abstract

The quality of many golf courses and other turfgrass areas often requires high levels of cultural management. The fact that this level of maintenance usually includes the use of preemergent herbicides has caused concern about their potential for ground water contamination. Much of this concern is based on extrapolation from agricultural situations rather than data developed from studies conducted in field turfgrass situations. To address this data gap, a two‐year field project evaluating the behaviour and mobility of the commonly used preemergent herbicides, benfluralin, trifluralin, bensulide, oxadiazon. pendimethalin, and DCPA with its two metabolites was conducted at OARDC/The Ohio State University, Wooster, Ohio, in 1988–89. Plots were located on a site with thatch (WT) and one with no thatch (NT)to further clarify the impact of thatch on herbicide behavior. Treatments were applied in April and samples of thatch and four zones of soil (0–2.5, 2.5–5, 7.5–10 and 22.5–25cm) were collected throughout the year and analyzed for residue dissipation. Residues of pendimethalin, benfluralin, and trifluralin in the 22.5–25 cm zone were below the limit of determination. No detectable oxadiazon residues were found in this zone at the WT site in 1988 but on two occasions, residues of 0.01 and 0.02 kg/ha were found in 1989. At the NT site, residues in this zone on one occasion were 0.02 kg/ha in 1988 and none in 1989. Residues of bensulide in the same zone ranged not detectable (ND)‐0.02 kg/ha in both locations. The DCPA residues in the 22.5–25 cm zone ranged ND‐0.10 kg/ha (WT), ND‐0.27 kg/ha (NT) in 1988. and ND‐0.02 kg/ha (WT), ND‐0.04 kg/ha (NT) in 1989. The residues of SDS 1449, the less stable of two dacthal metabolites, were very low but higher in 1988 than in 1989 in both locations. The SDS 954 residues in 22.5–25 cm zone ranged ND‐0.1 kg/ha (WT), and ND‐0.16 kg/ha (NT) in 1988, and ND‐0.26 kg/ha (WT), and ND‐0.27 kg/ha (NT) in 1989.

Some amount of all herbicides applied carried over into the spring of the year following application but oxadiazon and bensulide were the most persistent.     

Evaluation of the cytotoxic effects of glyphosate herbicides in human liver,lung, and nerve

Glyphosate-based herbicides are broad-spectrum pesticides widely used in the world, which is considered a highly safe pesticide due to their target specificity, but recently, there has been an ongoing controversy regarding their carcinogenicity and possible side effects of glyphosate on human health. Commercial glyphosate-based herbicides (GBHs) consist of declared active ingredient (glyphosate salts) and a number of formulants such as ethoxylated formulants (4130®, 3780^®, and A-178^®). The aim of our study is to investigate whether the toxicity of GBHs is related to formulants. The effects of GBHs on human health were studied at the cellular level based on their toxicity to liver, lungs and nerve tissue. The inhibitory toxicity to cell viability by GBHs was examined with cell-based systems using three human cell lines: HepG2, A549, and SH-SY5Y. Data obtained showed that all tested ethoxylated formulants and their mixtures with declared active ingredient glyphosate isopropylamine salt (GP) have significant inhibitory effect on cell proliferation, while the declared active ingredient has no significant toxicity. Our study demonstrates that the toxic effect of GBH is primarily due to the use of formulants. This result suggests that GP is relatively safe and a new approach for the assessment of toxicity should be made.     

钛石膏中重金属元素的浸出特性研究

研究了钛石膏中重金属含量和不同浸出条件下钛石膏中重金属的浸出特性。结果表明,钛石膏中Mn、Hg、Zn、Cr、As含量相对较高,表现出对周围环境的潜在危害性。不同浸提剂浸出实验中,由于较强的离子强度效应,海水对重金属的浸出能力强于硫酸/硝酸、去离子水(除Zn外),且海水Hg浸出浓度超出标准限值近3倍。在连续静态浸出实验中,海水浸出和酸性浸出的重金属浓度均不断降低,但重金属海水浸出量始终高于酸性浸出,表明盐度对重金属的浸出具有持续促进作用,而钛石膏则表现出较强的酸缓冲能力。同时在连续浸出过程中海水及酸性浸出的重金属累积浸出率均显著增加,说明在标准加速浸出时间以外,钛石膏液固浸出体系仍具有较强的重金属释放能力,故认为钛石膏简易堆存可能存在环境风险。     

AOD渣中铬的连续淋溶特性及其动力学模型的构建

为评价AOD(氩氧脱碳炉)渣的淋溶毒性,采用连续20 d的静态淋溶试验,研究了中性和酸性淋溶液对AOD炉渣中Cr(铬)淋溶特性的影响,以累积溶出率构建了Cr淋溶动力学模型. 结果表明:在连续淋溶过程中,淋溶液pH(9.6~11.5)始终保持碱性,DO(溶解氧)基本处于饱和状态,淋溶液还原性呈降低趋势;随着淋溶时间的延长,淋溶液中Cr6+、TCr和Cr3+的累积溶出率呈增加趋势,不同初始淋溶液pH(2.0、3.0、4.0、5.0、6.0、7.0)下,连续淋溶20 d时Cr6+、TCr和Cr3+的累积溶出率分别是淋溶2 d时的10.1~22.2、7.5~15.6、6.3~17.1倍;与中性和弱酸性淋溶液相比,连续淋溶20 d,酸性较强的淋溶液中Cr6+、TCr和Cr3+的累积溶出率分别为其3.1~6.6、1.6~3.2和1.8~2.1倍;与短期静态淋溶相比,连续淋溶增加了淋溶液总量,尽管ρ(Cr)变化较小,但TCr累积溶出率显著增加;双常数速率、抛物线和指数模型均可拟合淋溶液中Cr6+、TCr和Cr3+的累积溶出率,其中,抛物线模型的相关系数均在0.99以上,是最佳模型. AOD渣中Cr的连续淋溶动力学模型的构建可为不锈钢渣中Cr的淋溶毒性及其生态风险评价奠定试验和理论基础.      

工矿型绿洲农田土壤中氟和镉的剖面行为研究

以甘肃白银市城郊东区农田土壤为研究对象进行剖面取样、对土壤中氟和镉的剖面分布及行为进行研究.结果表明,在长期灌溉与降水渗水流作用下,F和Cd发生不同程度的淋溶迁移,F迁移深度达到80~100cm,Cd迁移深度在40~60cm,迁移程度为F>Cd;元素F和Cd都具有显著的负乘幂迁移规律,同时表现出不同的迁移态势,F 为高剂量时迁移率大,低剂量时迁移率小,但Cd呈现相反的迁移趋势.污水灌溉作为土壤污染物来源之一对土壤F和Cd累积和迁移有一定影响,F元素对当地地下水污染的威胁较大.     

镍钴采选行业废石和尾矿中重金属淋溶释放规律研究

镍钴采选废石和尾矿中重金属的溶出释放规律对矿区的重金属污染防治具有重要意义。但目前,国内还没有对镍钴行业采选产生的尾矿和废石中重金属的溶出规律开展研究。本文以镍钴采选企业的尾矿和废石作为样本,开展了毒性浸出实验。研究了不同pH值、离子强度、温度等实验条件对重金属溶出的影响,探讨了镍钴采选过程中所产生的尾矿和废石中重金属的溶出特性和释放规律。实验结果表明,尾矿样品中Ni的浸出浓度为42.28 mg·L^-1,是最大允许排放浓度的8.86倍,为具有浸出毒性特征的危险废物;废石样品中重金属Ni和Cu的溶出浓度分别为4.72 mg·L^-1和26.2 mg·L^-1,超过最大允许排放浓度,属于第Ⅱ类一般工业固体废物。pH对样品中Ni、Cr、Pb、Co和As的溶出量影响较大,其中尾矿中Ni和Cu在pH较低的条件下,可达到44.28 mg·L^-1和53 mg·L^-1,远高于最大允许排放浓度,而Hg、Cd和Cu的溶出量随pH值的变化不大。除As以外,样品中大多数重金属的溶出质量浓度在酸性条件下比在中性条件下高,这表明在酸性环境条件下,这些重金属对周围生态环境的潜在风险更大。离子强度的变化对Cd和Co的溶出量的变化并不明显,而当离子强度变化时,Ni、Cr、Pb、Hg、Cu和As的溶出量可能达到最大,使周围环境的潜在生态风险增大。当温度达到35~40℃时,部分重金属如Co、Pb、Cd 等,溶出量将达到最大;当温度低于25℃时,除 Ni 以外,大部分重金属溶出量很低。而温度变化对重金属Cu、As、Cr和Hg的溶出量的影响不明显,波动范围较小,对周围生态环境产生的潜在生态风险较小。     

热带亚热带土壤氮素反硝化研究进展

热带亚热带独特的土壤性质可能使得反硝化机理有别于温带土壤.文章综述了热带亚热带地区土壤氮素生物反硝化的研究进展,试图更好地了解该地区土壤反硝化在全球氮（N）循环以及在全球环境变化和生态系统响应互作中的角色.热带亚热带土壤反硝化强度普遍较温带地区弱,且随着土地利用方式和耕作管理措施的不同而呈现较大的时空变异性.影响土壤水分状况和土壤碳（C）、N 转化特性和速率的因素即为区域和农田尺度上的反硝化影响因素.湿润型热带亚热带土壤由于含有丰富的氧化物而致使土壤氧化还原势较高,这也是导致该地区土壤反硝化势较温带地区较低的关键土壤因素之-.然而土壤pH 值不是该地区土壤反硝化势较低的主要限制因素.有机C 矿化过程较土壤全氮含量和土壤C/N 比在决定湿润型亚热带土壤反硝化势方面更为重要.愈来愈多的证据表明热带亚热带土壤反硝化的生态环境效应不同于温带地区,热带亚热带地区土壤反硝化对全球变暖的贡献应综合考虑其对其它温室气体（如CH4,CO2）排放和氮沉降的影响.热带亚热带土壤生态系统具有-些防止土壤氮素反硝化损失的机制和保氮策略.然而,热带亚热带生态系统对全球变化的响应机制及其生物地球化学调控机制仍然不清楚,这些研究对于反硝化和其它同时发生的氮转化过程模型的精确构建至关重要.     

猪粪还田对土壤硝态氮淋失的影响研究——以黄灌区稻旱轮作制为例

宁夏引黄灌区是水污染严重地区之一,大部分排水沟水质属于劣五类,主要污染物是硝态氮与铵态氮.猪粪还田试验共有3个处理:传统施肥+空白(CK)、传统施肥+猪粪还田4500 kg/hm²(T1)和传统施肥+猪粪还田9000 kg/hm²(T2).采用树脂芯法测定了30,60,90cm土层的硝态氮淋失量.结果表明,30cm土层处,猪粪还田没有明显增加土壤硝态氮淋失.与对照(15.96±0.41) kg/hm²相比,T1(16.85±0.40) kg/hm²与T2(17.01±0.46) kg/hm²没有达到显著差异(P>0.05);60cm土层处理与对照也没有达到显著差异;90cm土层处的猪粪处理与对照达到显著差异,处理之间没有差异.猪粪还田有利于土壤有机质和总氮提高,30cm土层,与对照相比,T1和T2的有机质增加0.95g/kg和1.41g/kg,分别提高7.50%和11.13%;总氮增加0.06和0.16g/kg,分别提高7.72%和22.04%.猪粪还田提高了作物产量,水稻增产12.26%~11.56%,冬小麦产量提高9.32%~12.52%.