水生生物水质基准研究中轮虫、水螅、涡虫类受试生物的筛选

轮虫、水螅、涡虫是水生生态系统的重要生物类群。因其对水体污染较敏感,所以对水生生物基准研究有重要意义。依据我国生物区系资料及毒性数据丰度,筛选出8种代表性本土轮虫、水螅、涡虫类生物。参照美国水生生物基准技术指南,搜集、筛选了这8种代表性生物的急性毒性数据,通过数据分析,筛选出对各物种毒性最大的污染物,主要包括重金属、农药、有机锡化物、表面活性剂、吡啶胺类杀菌剂。分析污染物的物种敏感度分布,依据累积概率对代表性生物的物种敏感性进行分类,结果为:萼花臂尾轮虫(Brachionus calyciflorus)、绿水螅(Hydra viridissima)、普通水螅(Hydra vulgaris)对重金属铜的累积概率为6.5%、8.5%和10.4%,普通水螅(Hydra vulgaris)对重金属汞的累积概率为6.3%;龟甲轮虫(Keratella cochlearis)和四齿腔轮虫(Lecane quadridentata)对五氯酚钠的累积概率为5.1%和7.6%;褐水螅(Hydra oligactis)和绿水螅(Hydra viridissima)对三丁基氧化锡的累积概率为6.9%和13.8%,萼花臂尾轮虫(Brachionus calyciflorus)对氟啶胺的累积概率为6.7%,日本三角涡虫(Dugesia japonica)对四氯化碳、十二烷基苯磺酸钠的累积概率分别为6.7%和7.1%。上述结果表明:萼花臂尾轮虫、绿水螅对重金属铜敏感;普通水螅对重金属铜和汞敏感;龟甲轮虫和四齿腔轮虫对农药敏感;褐水螅和绿水螅对有机锡化物敏感;萼花臂尾轮虫对吡啶胺类杀菌剂敏感;日本三角涡虫对四氯化碳、表面活性剂敏感。这7种代表性生物可作为相关污染物的水生生物基准受试物种。     

贵州省典型矿区土壤重金属污染对蚯蚓的毒性效应评估

选取我国贵州省某矿区典型的重金属复合污染土壤开展28 d慢性毒性暴露试验,以蚯蚓体内2种抗氧化酶活性——过氧化氢酶(CAT)和超氧化物歧化酶(SOD)、8-羟基脱氧鸟苷(8-ODHG)和金属硫蛋白(MT)含量为生物指标,评估了以上生物指标与土壤重金属含量的相关性,探讨该研究方法用于矿区土壤重金属生态风险评估的可行性。结果表明,CAT和SOD在暴露周期内均出现先诱导后抑制的动态响应过程,表明蚯蚓通过提高CAT和SOD的活性来清除机体因污染胁迫而产生的自由基,以适应环境变化,在毒性缓解后,蚯蚓体内代谢产物的积累抑制了抗氧化氢酶活性,CAT和SOD活性下降并趋于稳定。暴露于重金属污染亚致死浓度时,蚯蚓体内的8-OHDG含量随着暴露时间的延长显著降低,随着暴露浓度的增加,损伤存在由低到高的转变。在28 d暴露周期内,蚯蚓体内MT在重金属胁迫下发挥了解毒作用,MT含量在蚯蚓暴露后第7天增加,随后逐渐降低。本文基于生物毒性试验综合评估了矿区典型重金属污染土壤的生态风险,研究结果对指导重金属复合污染土壤的修复与再利用具有重要意义。     

溴氰菊酯对菲律宾蛤仔体内酶活性和组织损伤的初步探索

采用不同质量浓度的溴氰菊酯(0.0070 mg·L~(-1)、0.014 mg·L~(-1)、0.020 mg·L~(-1)、0.027 mg·L~(-1))对菲律宾蛤仔进行20 d半静置染毒,测定不同时间淋巴液中乙酰胆碱酯酶(ACh E)和钠离子-钾离子-三磷酸腺苷酶(Na~+-K~+-ATPase)活性、鳃和肝脏中谷胱甘肽转硫酶(GST)活性的变化,并观察染毒20 d后鳃丝组织和消化盲囊组织的损伤情况。酶活性分析结果显示,与对照组相比,低浓度组(0.0070 mg·L~(-1))试验期间酶活性均无显著差异(P0.05);中浓度组(0.014 mg·L~(-1)、0.020 mg·L~(-1))淋巴液中ACh E和Na~+-K~+-ATPase均呈先激活后抑制的变化规律(P0.05),鳃和肝脏中GST活性均呈上升趋势(P0.05);高浓度组(0.027mg·L~(-1))淋巴液中ACh E和Na~+-K~+-ATPase、肝脏中GST活性在试验期间持续下降(P0.01),而鳃中GST活性呈先抑制后升高的趋势(P0.05)。研究表明,低中浓度的溴氰菊酯对菲律宾蛤仔体内的酶活性表现为先诱导后抑制,具有明显的时间、剂量效应;高浓度的溴氰菊酯对菲律宾蛤仔体内酶活持续抑制,且染毒浓度越高,组织细胞变异越显著,表现为鳃丝上皮细胞纤毛层萎缩、纤毛脱落,消化盲囊上皮细胞膨胀,出现包涵体样结构。     

Toxicity evaluation of 10 oil gelling agents北大核心CSCD

Oil gelling agents are widely used in emergency response of marine oil spills. However, the biological toxicity of oil gelling agents is not well understood. This research aimed to evaluate the environmental safety of oil gelling agents used for rapid removal and cleanup of marine oil spills. We used luminescent bacteria (Acinetobacter sp. Tox2 and Acinetobacter sp. RecA) combined with exposure experiment using marine medaka (Oryzias melastigma) juveniles to detect the acute toxicity and genotoxicity of 10 oil gelling agents. As a result, a certain level of acute toxicity was detected from the oil gelling agent FOA and GMN-01 (the toxicity equivalent to 0.067 mg/L and 0.084 mg/L of HgCl2, respectively), and a certain level of genotoxicity was detected from the oil gelling agent NORSOREX (the toxicity equivalent to 0.307 mg/L of MMC) by the luminescent bacteria test. However, no obvious acute toxicity or genotoxicity was detected from the above three oil gelling agents in fish-exposure experiments. Our results suggest that the 10 oil gelling agents have no obvious acute toxicity or genotoxicity to higher organisms (including marine medaka). The luminescent bacteria test is more sensitive in detecting biological toxicity of oil gelling agents. This study provides a reference for environmental safety evaluation of the oil gelling agents used in the cleaning up of the marine oil spills.     

垃圾填埋场渗滤液溶解性有机质特性及其去除技术综述

垃圾填埋场渗滤液所含物质种类繁多,理化特性复杂,且随填埋时间等条件而变化.本文综合分析了垃圾渗滤液溶解性有机质的组成特征、结构特征及随年代变化特征.针对垃圾渗滤液难降解有机质的特性而研发的处理技术包括物化法、高级氧化法和微电解法等,并在实际工程中得到应用.随着越来越严格的渗滤液排放要求,溶解性有机质的去除应充分考虑投资的经济、运行的稳定性和可靠性.     

Changes in nitrogen budget and potential risk to the environment over 20 years(1990–2010) in the agroecosystems of the Haihe Basin,China

The nitrogen balance can serve as an indicator of the risk to the environment of nitrogen loss from agricultural land. To investigate the temporal and spatial changes in agricultural nitrogen application and its potential threat to the environment of the Haihe Basin in China, we used a database of county-level agricultural statistics to calculate agricultural nitrogen input, output,surplus intensity, and use efficiency. Chemical fertilizer nitrogen input increased by 51.7% from1990 to 2000 and by 37.2% from 2000 to 2010, concomitant with increasing crop yields.Simultaneously, the nitrogen surplus intensity increased by 53.5% from 1990 to 2000 and by16.5% from 2000 to 2010, presenting a continuously increased environmental risk. Nitrogen use efficiency decreased from 0.46 in 1990 to 0.42 in 2000 and remained constant at 0.42 in 2010,partly due to fertilizer composition and type improvement. This level indicates that more than half of nitrogen inputs are lost in agroecosystems. Our results suggest that although the improvement in fertilizer composition and types has partially offset the decrease in nitrogen use efficiency, the environmental risk has still increased gradually over the past 20 years, along with the increase in crop yields and nitrogen application. It is important to achieve a better nitrogen balance through more effective management to significantly reduce the environmental risk,decrease nitrogen surplus intensity, and increase nitrogen use efficiency without sacrificing crop yields.     

罗布泊“大耳朵”地区沉积物重金属含量及空间分布特征

以罗布泊"大耳朵"地区为研究区域,利用石墨炉原子吸收分光光度计(GF-990)和火焰原子吸收分光光度计(AAS-990)分析测试了沉积物中Pb、Cu、Ni和Mn元素的总量,并测定了沉积物中有机质的含量,运用SPSS软件分析了各重金属总量与有机质之间的相互关系。结果表明:罗布泊"大耳朵"地区盐壳层沉积物中Pb含量的变化范围在2.57~58.63 mg/kg,Cu含量的变化范围在6.33~39.65 mg/kg,Ni含量的变化范围在5.55~46.33 mg/kg,Mn含量的变化范围在46.33~1474.60 mg/kg;除Pb的垂直分布随着深度的增加其含量减少并趋于稳定外,重金属Cu、Ni和Mn的总量在各剖面垂直方向上大部分呈波折多峰行分布,分布趋势差异较大;重金属Pb、Cu、Ni和Mn与有机质都存在显著相关性。     

钦杭结合带加里东期榴闪岩超高压变质作用研究

对钦杭结合带首次发现的加里东期榴闪岩进行了详细的年代学、矿物学和变质作用研究。结果表明,榴闪岩的变质时代为454±4Ma,经历了早期角闪岩相进变质、中期榴辉岩相峰期变质和晚期角闪岩相退变质三个阶段,具顺时针P-T-t轨迹。早期角闪岩相进变质作用阶段的矿物共生组合为角闪石+斜长石+石英,温压条件分别为719℃~795℃和7.56Kpa~8.30Kpa;中期榴辉岩相峰期变质作用阶段的矿物共生组合为石榴子石+绿辉石(后期退变为透辉石+钠长石)±石英,温压条件分别为668℃~821℃和26.42Kpa~33.46Kpa;晚期角闪岩相退变质作用阶段的矿物共生组合为石榴子石+角闪岩+斜长石±石英(即榴闪岩),相应的温压条件分别为611℃~854℃和4.76Kpa~9.30Kpa。结合前人资料推断,区域内加里东期可能经历了榴辉岩相超高压变质→高温麻粒岩相退变质→角闪岩相退变质的演化过程。钦杭结合带首次厘定出加里东期超高压变质作用,表明华夏和扬子两大陆块碰撞拼合发生在加里东期。     

Flower-, wire-, and sheet-like MnO2-deposited diatomites: Highly efficient absorbents for the removal of Cr(VI)

Flower-, wire-, and sheet-like MnO₂-deposited diatomites have been prepared using a hydrothermal method with Mn(Ac)₂, KMnO₄ and/or MnSO₄ as Mn source and diatomite as support. Physical properties of the materials were characterized by means of numerous analytical techniques, and their behaviors in the adsorption of chromium(VI) were evaluated. It is shown that the MnO₂-deposited diatomite samples with different morphologies possessed high surface areas and abundant surface hydroxyl groups (especially the wire-like MnO₂/diatomite sample). The wire-like MnO₂/diatomite sample showed the best performance in the removal of Cr(VI), giving the maximum Cr(VI) adsorption capacity of 101 mg/g.