阿哈水库沉积物总汞及甲基汞分布特征

为弄清阿哈水库沉积物是否受到历史矿山废水输入对沉积物总汞及甲基汞垂直分布的影响,对沉积物总汞及甲基汞的含量和其垂直分布特征进行了研究.结果表明,阿哈水库沉积物总汞含量变化范围为160～252 ng·g-1,平均为210 ng·g-1,明显高于其他未受到污染的水库沉积物.沉积物中总汞含量随沉积物深度增加呈增加趋势,与其沉积环境有关.沉积物中甲基汞含量变化范围为0.2～7.2 ng·g-1,平均为1.8 ng·g-1,丰水期甲基汞含量随深度增加逐渐下降,且沉积物表层甲基汞含量显著高于枯水期,与丰水期表层有机物的增加和厌氧环境有关.     

长白山森林地区河流中汞的时空分布特征

采集并测定了枯水期和丰水期长白山北坡几条河流的水样,研究了长白山地区河流中总汞和甲基汞的时空变化规律.长白山北坡地区河流总汞的变化范围为2.0～20 ng·L-1,受北方燃煤等人为活动影响,枯水期总汞含量高于丰水期;甲基汞的变化范围为0.12～0.55 ng·L-1,不同季节的甲基汞变化不大.水体汞含量随海拔的升高而降低,汇入松花江的几条河流对松花江水体的影响较为明显,随着河流的汇入溶解态汞含量下降,颗粒态汞含量升高.与世界上其他一些森林水体对比发现,长白山水体甲基汞含量较低,但总汞含量较高.估计研究地区河流一年将向下游地区输出33 kg的总汞以及200 g甲基汞,这将进一步加剧下游水体汞的负担.     

长白山北坡森林土壤汞的含量和形态分布

分别于2009年4月和9月对长白山北坡的土壤样品进行了采集,研究北方森林地区不同海拔土壤样品中的总汞和甲基汞的分布情况.长白山土壤THg和MeHg含量分别为0.08～0.73 mg·kg-1和0.05～0.56 μg·kg-1,库存量分别为97 kg·km-2和128 g·km-2,高于吉林省背景值,MeHg的最高含量...     

乌江洪家渡水库鱼体汞含量

测定了贵州省乌江流域新建的洪家渡水库中的8种124尾鱼类的总汞和甲基汞含量,探讨其变化趋势及可能产生的生态风险。总汞采用混合酸消解用冷原子荧光(CVAFS)测定,甲基汞的测定采用碱消解-水相乙基化结合气相色谱(GC)冷原子荧光(CVAFS)测定。结果表明,总汞和甲基汞含量均为肉食性鱼类杂食性鱼类,鱼体汞含量与它们的生态学特性(食物来源和生活习性)有关,与体重和体长无显著相关关系;鱼体总汞和甲基汞含量均值分别为0.063±0.046和0.028±0.019mg.kg-1,均远低于大部分研究报道的新建水库中鱼体汞含量(0.50mg.kg-1)。洪家渡水库鱼类由于在低汞环境中,导致甲基汞不易富集,其鱼体甲基汞和总汞含量并未急剧增加,显著不同于北美和欧洲等地区新建水库中鱼体汞含量升高的现象,但随着水库演化导致水库有机质增加可能使鱼体汞逐步上升。     

长江三峡库区江段沉积物的重金属污染特征

测定了三峡库区江段沉积物中２１个元素的含量,比例比配统计分析指出,重庆至涪陵江段的沉积物样品间无明显相关,涪陵至巴陵段的沉积物间在９０％置信水平上显著相关;沉积物中钙、镁、锶、钡、铁、钴、镍、镉、锰、锌、铝、钒、镧、钇、钛等元素间在９０％置信水平上有显著相关,伸砷、镉、铜、汞、铜、磷等元素间以及它们与上述元素间无显著相关,这表明涪陵以上江段的沉积物因受重庆和长春污染影响大,样品间的相似性小,而涪陵     

贵阳市大气降水中汞的分布特征

于2008年7-9月对贵阳市中心城区采集的21个大气降水进行了总汞、甲基汞及阴、阳离子浓度的测定,分析了大气降水中总汞与阴阳离子间的相互关系.结果表明:大气降水中总汞的平均含量为18 ng·L-1,变化范围为0.4～57.4 ng·L-1;甲基汞的平均含量为0.07 ng·L-1,变化范围为0.02～0.2 ng·L-1.大气降水中的阴离子以SO2-4和NO-3为主,其浓度平均值分别为151和145 mol·L-1;阳离子主要以Ca2+为主,平均浓度达到了123 mol·L-1,变化范围为3.7～560 mol·L-1,其次是NH4+和Mg2+,其浓度平均值分别为52.2和20.4 mol·L-1.通过分析降水中总汞和阴阳离子之间的相互关系,发现总汞和阴离子SO2-4具有显著的相关性,与F-有一定的相关性,而与NO-3不具有相关性.由此初步判定,大气降水中的总汞主要来源于燃煤等人为释放源.     

中亚热带常绿阔叶林凋落物分解过程中汞的动态变化及迁移机理

森林凋落物对于汞在林地土壤的生物地球化学循环中起到重要作用,为研究森林凋落物分解过程中汞的迁移转化特征,以重庆四面山风景名胜区典型林分(常绿阔叶林)作为研究对象。于2014年3月—2015年3月连续监测典型林分凋落物中各形态汞浓度和有机质变化量,同时监测周围土壤中汞浓度变化。结果表明:四面山典型林分凋落物分解过程中汞浓度整体上升,总汞浓度(初始浓度:78 ng/g)的增幅最高达53%,甲基汞浓度(初始浓度:0.32 ng/g)最高增幅达138%;在春季和夏季,水溶态和酸溶态两种活性态汞含量分别增加了851%和96%,在分解前期和末期,凋落物汞的中惰性汞比例最高,占比达75%。土壤腐殖质层中总汞和甲基汞浓度比较稳定。凋落物中活性态汞通过雨水淋洗进入土壤与有机质络合并发生甲基化/去甲基化过程,通过地表径流、地下径流进入水体。凋落物中C含量减少了22%,N含量增加了15%,总汞浓度与C/N比呈负相关,与N含量呈正相关。凋落物中微生物C、N含量整体增加,与汞浓度峰值同步,且夏季含量显著高于冬季含量(P0.05),说明微生物与凋落物固定汞和汞的甲基化过程密切相关。     

汞的微生物甲基化研究进展

汞的微生物甲基化作用是汞生物地球化学循环过程中重要环节之一,与人类健康密切相关.近年来,该领域的研究受到越来越多的关注.本文综述了汞的微生物甲基化研究的历史与发展现状、汞微生物甲基化的影响因素、甲基化的机制和目前的主要研究方法等.确定特定生态系统中的汞甲基化微生物种类,明确甲基化机制及影响因素,以及探讨汞微生物甲基化过程中导致的汞同位素分馏等,将成为本领域的研究热点及重点.     

网箱养鱼对水库水体甲基汞的影响

分别在2010年9月(暖季)和2011年3月(冷季),选取乌江渡水库网箱养鱼区和距离网箱100～200m的对照区(库心),对水体不同形态汞及其他相关参数进行了研究,以揭示网箱养鱼对水库汞地球化学行为的影响。结果表明,暖季养鱼区水体总汞含量为(2.04±0.53)ng·L-1,甲基汞含量为(0.146±0.231)ng·L-1,对照区水体总汞含量为(3.33±2.39)ng·L-1,甲基汞含量为(0.380±0.577)ng·L-1;冷季养鱼区水体总汞含量为(3.04±1.53)ng·L-1,甲基汞含量为(0.047±0.028)ng·L-1,对照区水体总汞含量为(3.24±1.23)ng·L-1,甲基汞含量为(0.046±0.013)ng·L-1;养鱼区与对照区总汞含量(n=35,P=0.875)、甲基汞含量(n=35,P=0.091)均无显著差异。结合对养鱼区与对照区水体中其他各参数(总氮、总磷、溶解性有机碳、叶绿素、温度、溶解氧等)综合分析表明,由于水库蓄水与泄水发电对水库水体的扰动及水库自身水体的交换作用导致水体呈混匀状态,网箱养鱼造成的水体甲基化程度差异不显著;而水库水体季节性分层造成的水体底部厌氧和温度的变化是影响水体甲基汞含量及分布的主要因素之一。     

Mercury Contamination and Dynamics in the Sediment of the Second Songhua River,China

The Second Songhua River (SSR) was subjected to a large amount of mercury discharge from petrochemical industries in Jilin City from the 1960s to 1980s. The objectives of this study were to investigate the spatial and temporal change of mercury concentration in the sediments of the river and to assess Hg pollution in sediment employing enrichment ratio. Bottom sediments sampled in 2005 were digested with various acids followed by analysis by atomic fluorescence spectrometry for Hg, ICP-MS for Cd, Pb and Sc, and ICP-OES for Co, Cr, Cu, Zn, Mn, Ni, P, Pb, Sb, Ti, V, Al, Fe, Mg, Ca, Na, and K, in order to measure the total concentrations of these elements in the sediments. Results indicated that mercury concentrations in the sediments were strongly related with distance from the historic industrial point source, decreasing at an exponential rate from 1.27 mg kg^?1 at Jilin City to 0.01 mg kg^?1 at downstream Haerbin City. In addition, mercury concentration decreased from 16.8 mg kg^{? 1} y^?1 in 1974 to 0.09 mg kg^?1 y^?1 in 2005 in the sediments at effluent discharge site, and from 0.006 mg kg^?1 y^?1in 1974 to 0.004 mg kg^?1 y^?1 in 2005 at Songyuan City 257 km downstream. In the sedimentary sections of the river, deeper sediments contained higher concentrations of mercury as compared to the surface sediments, suggesting discharges of higher levels of mercury in the past and its subsequent burial over the years by less polluted sediments. Background concentrations of mercury in the surface sediments, reconstructed by tracer Sc, were 0.011 to 0.018 mg kg^?1. Enrichment ratios of Hg in the sediments of SSR was 5 to 75, indicating moderate to extreme pollution, while the sediment of Songhua River is less contaminated, with enrichment ratios of 0.9 to 1.5. At present, the previously accumulated and buried mercury in sediments may not significantly affect water quality of the SSR, but might pose a potential ecological risk to aquatic and amphibian animals. Natural attenuation seems to be an economic remedial choice for these sediments.     

福建漳江口红树林沉积物重金属汞(Hg)的分布特征

对福建漳江口红树林沉积物中重金属汞(Hg)含量的时空分布进行了研究。结果表明漳江口红树林湿地汞含量为0.0815 mg•kg–1—0.3431 mg•kg–1。在潮间带水平分布上, 从光滩到高潮位汞含量显著上升(P<0.05), 相对光滩, 红树林沉积物更易富集汞, 其中高潮位红树林底泥中汞含量最高。在垂直方向上, 大多数的汞富集在表层及亚表层, 随着深度的加深, 汞含量呈现下降趋势。汞在红树林湿地沉积物中的积累主要与有机碳(TOC), 含水率, 盐度相关。从计算的单一污染指数(Pi)来看, 漳江口地区汞污染等级为Ⅲ级以下, 大多数采样点属于自由污染或轻度污染。就该地区汞污染的时空变化趋势以及和其他红树林区汞污染状况的对比来看, 漳江口地区存在一定程度的汞污染威胁加剧的现象, 值得引起注意。     

Geospatial Estimation of Mercury Contamination in Buffalo River Sediments

The Buffalo River Area of Concern (AOC) is associated with heavy metal pollution. This research utilized sediment core data to model the geographic distribution of mercury within surface and subsurface sediments of a section of the AOC. Using ordinary kriging, a geostatistical interpolation technique, mercury concentration prediction maps were created. Standard maps were created by interpolating a prediction surface for the entire study area. In addition, spliced maps were created by interpolating prediction surfaces for three sections of the study area and merging these together to generate a quasi-continuous surface. The latter type of map was needed in order to account for the pronounced meandering nature of the river and to explore the potential existence of regional and local mercury sedimentation patterns. The surface level results show an increased level of mercury contamination from east to west (the direction of river flow), with peak values found in the mid-region of the study area. Additionally, surface sediments were less polluted with mercury than subsurface sediments. Finally, this study highlighted several mercury contamination hotspots, which could be targeted for future sediment restoration endeavors in the AOC.     

Behavior of mercury in the Patuxent River estuary

An overview of a comprehensive study of the behavior and fate of mercury in the estuarine Patuxent River is presented. Total Hg (Hg_T) and methylmercury (MeHg) exhibited weakly non-conservative behavior in the estuary. Total Hg concentrations ranged from 6 ng L^-1 in the upper reaches of the sub-urbanized tidal freshwater river to <0.5 ng L^-1 in the mesohaline lower estuary. Filterable (0.2 µm) Hg_T ranged from 0.2 to 1.5 ng L^-1. On average, MeHg accounted for <5% of unfiltered Hg_T and <2% of filterable Hg_T. Dissolved gaseous section Hg (DGHg) concentrations were highest (up to 150 pg L^-1) in the summer in the mesohaline, but were not well correlated with primary production or chlorophyll a, demonstrating the complex nature of Hg⁰ formation and cycling in an estuarine environment. Organic matter content appeared to control the Hg_T content of sediments, while MeHg in sediments was positively correlated with Hg_T and organic matter, and negatively correlated with sulfide. MeHg in sediments was low (0.1 to 0.5% of Hg_T). Preliminary findings suggest that net MeHg production within sediments exceeds net accumulation. Although Hg_T in pore waters increased with increasing sulfide, bulk MeHg concentrations decreased. The concentration of MeHg in sediments was not related to the concentration of Hg_T in pore waters. These observations support the hypothesis that sulfide affects the speciation and therefore bioavailability of dissolved and/or solid-phase Hg for methylation. Comparison with other ecosystems, and the negative correlation between pore water sulfide and sediment MeHg, suggest that sulfide limits production and accumulation of MeHg in this system.     

渭河陕西段沉积物重金属空间分布及来源解析

为了了解渭河陕西段河道沉积物重金属空间分布特征,本研究对渭河陕西段干流及其支流17个采样点沉积物中的10种重金属元素(Cd、Sb、As、Co、Cu、Pb、Ni、Cr、Zn、Mn)含量进行测定及来源辨析。结果表明: 重金属元素Cd、Sb、As、Co、Cu、Pb、Ni、Cr、Zn、Mn的平均含量分别为0.10、1.24、11.73、11.95、24.90、24.91、29.31、54.18、72.74、626.85 mg·kg^-1, 除Cd的变异系数大于1以外,其他元素的变异系数均低于0.5。其中,Cd、Pb、Cr含量于灞河入渭处达到峰值,Co和Mn在黑河入渭处达到峰值,Cu和Zn在清姜河入渭处达到峰值, Sb、As和Ni分别于沙王渡、咸阳铁桥和林家村处达到峰值。相关性分析、主成分分析和聚类分析表明,Cd、Co、Cu、Pb、Ni、Cr、Zn、Mn主要来源于以工业源和生活源为主的污染源;Sb、As主要来源于农业和地球化学污染源。     

Mercury dynamics in Tivoli South Bay, a freshwater tidal mudflat wetland in the Hudson River

The accumulation of total mercury (Hg_T) andmethylmercury (MeHg) was evaluated in sediments ofTivoli South Bay, a freshwater tidal mudflat wetlandin the Hudson River National Estuarine ResearchReserve system. Hg_T concentrations in sedimentcores were measured to evaluate the spatialvariability of Hg_T deposition, and to establisha chronology of Hg_T accumulation. Cores takenfrom the northern, middle, and southern sections ofthe bay had similar distribution patterns andconcentrations of Hg_T, suggesting a common sourceof Hg_T throughout the bay. Sedimentconcentrations ranged from 190 to 1040 ng Hg g^–1,2 to 10 times greater than concentrations expected insediments from non-anthropogenic sources. Hg_Tdeposition rates were similar in different regions ofthe bay, and increased from 200 ng Hg cm^–2yr^–1in the 1930s to a maximum of 300 ngHg cm^–2 yr^–1 in the 1960s. Deposition rateshave steadily declined since the 1970s and arecurrently at 80 ng Hg cm^–2 yr^–1. Transportof Hg_T by tidal waters from the Hudson River islikely the main source of Hg_T in the bay.Distribution patterns and absolute concentrations ofMeHg in sediment cores were similar throughout thebay, with concentrations ranging from 0.43 to 2.95ng g^–1. Maxima in MeHg concentration profilesoccurred just below the sediment-water interface andat a depth of 30 cm. The maximum at 30 cm wascoincident with maximum Hg_T concentrations. MeHgconcentrations in suspended particulate matter (SPM)from the Hudson River suggest that MeHg in the baycould be derived from riverine SPM rather than formedin situ.     

Distribution and contamination assessment of arsenic and mercury in surface sediments from the intertidal zone of Yantai Sishili Bay,China

Sixty surface sediment samples from the intertidal zone of Yantai Sishili Bay (YSB) have been analyzed for arsenic (As) and mercury (Hg) to evaluate their contamination levels and potential ecological risks. Concentrations of As and Hg ranged from 7.01–23.56 and 0.00–0.01 μg g^?1 in the dry season; during the wet season, the corresponding data were 1.44–6.17 and 0.00–0.02 μg g^?1. The geoaccumulation index (I_geo) and potential ecological risk index (E_rⁱ) were used to conduct a pollution assessment. The results demonstrated that the intertidal zone of YSB has good sediment quality and that As and Hg are not likely to cause negative environmental impacts in the region.