新疆喀什三角洲地下水SO2-4化学特征及来源

"水质型"缺水问题是新疆喀什地区水资源紧缺的主要原因之一.位于喀什地区西部的喀什三角洲面积13 329 km~2,73. 2%面积的潜水和53. 2%面积的承压水SO_4~(2-)浓度超过地下水质量Ⅲ类标准,同时伴随有高TDS、高硬度等特征.运用δD、δ~(18)O-H_2O和δ~(34)S-SO_4~(2-)同位素等手段分析地下水SO_4~(2-)化学特征及来源.结果表明:①区内剥蚀山区钙质粉砂岩、钙质细砂岩和石膏等盐类矿物的溶解控制了流域水化学组成,形成了水化学类型以SO_4型为主的地表水和地下水.地下水化学类型演变方向为HCO_3·SO_4→SO_4→SO_4·Cl,山麓斜坡冲洪积砾质平原为溶滤-径流带,河流冲积平原为径流-累积带,上游至下游地下水化学成分趋向盐化;②区内地下水初始补给源主要为大气降水,且受一定蒸发作用影响.不同水文地质单元地下水δD和δ~(18)O分布特征明显,上游至下游,同位素值由低到富集,受蒸发作用由弱到强;冲积平原承压水同位素分布较离散,受到上覆潜水混合作用影响;③南部、北部山麓斜坡冲洪积砾质平原潜水SO_4~(2-)来源分别为海陆交互相和陆相蒸发岩的溶滤;河流冲积平原潜水SO_4~(2-)除了陆相蒸发岩溶滤来源外,还存在化肥淋滤的污染;承压水受蒸发岩溶滤外,还受到潜水的混合作用和细菌还原硫酸盐作用影响.     

丹江流域山区地表水-地下水水化学特征及其影响因素

丹江流域是南水北调中线工程重要水源涵养区,深入研究丹江流域水化学特征及其影响因素,对区域水资源保护及合理利用具有重要意义.通过对丹江流域水样采集与分析,综合运用描述性统计、Piper三线图、Gibbs图、离子比例系数法及氢氧同位素的方法,分析丹江流域水化学特征及其影响因素.结果表明,丹江流域水体整体呈弱碱性,主要水化学类型为HCO3-Ca型,中游离子质量浓度及水化学类型变化频繁.流域水体均受大气降水补给,地表水受蒸发作用影响明显,水化学组分受岩石风化溶解、离子交换和人类活动共同影响. Ca2+和Mg2+源于方解石、白云石及石膏等碳酸盐和硫酸盐矿物溶解,农业活动是水中硝酸盐的主要来源.地表水与地下水频繁转化和支流汇入影响是丹江干流空间分布特征差异化的主要原因.     

植被恢复中坡地土壤颗粒有机碳分布特征和δ~(13)C值组成

以喀斯特地区植被恢复过程中典型坡地为研究对象,对坡地各个地形剖面土壤及土壤不同粒径组分中有机碳含量和有机质稳定碳同位素(δ13C值)组成进行了分析.结果显示:坡地土壤有机碳含量向下坡方向逐渐降低,上坡位两个剖面土壤砂粒(50～2000 um)中有机碳含量占50%以上,处于不稳定状态;易受到侵蚀作用破坏;而下坡位两个剖面中有机碳主要储存在粉粒(2～50um)和粘粒(<2um)土壤中,属于高度腐殖化的稳定有机碳.土壤有机质的δ13C值是评估SOC周转的一个良好指标,因粒径组成、剖面深度.植被和成土环境而不同.坡地各个土壤剖面中δ13C值的组成差异,较好地反映作物残体输入和土壤累积特征;输入土壤中的植物有机体由于分解程度不同而储存在不同粒径土壤中,因此各粒径中δ13C值对土层中有机质的储存和变化趋势具有较好的指示作用.     

Role of peat organic matter on isotopic composition of most abundant benthic organisms in intertidal habitats of SW Iceland

The transfer of peat organic matter (OM) from tidal pools of upper littoral to downstream rocky shores and its potential incorporation into marine biota were investigated using the stable isotope approach. Samplings were carried out in September 2004 in two SW Icelandic sites (Osar and Hvassahraun), where we selected (1) areas with shores where grass gently declined towards rocks and, on reaching the sea line, formed small tidal peat pools and (2) areas where grass and rocky shores were not contiguous, rather the grass lower limits were several hundreds of meters back from the shore. In both grass and no grass areas, in the intertidal zone, all benthic organisms and all potential OM sources were sampled. Dominant macroalgae were Ascophyllum nodosum ([Linnaeus] Le Jolis) and Fucus vesiculosus Linnaeus. In grass sites, organisms partially reflected the isotopic composition of peat OM, while in no grass sites, peat represented only a negligible amount of available OM, or its signal was totally absent from the environment. Intertidal organisms could rely on peat both directly by suspension feeding, grazing or scavenging and indirectly by predation (crabs) on low level consumers (barnacles).     

贵州省务川汞矿区汞污染的初步研究

对贵州省务川汞矿区的大气、地表水和土壤中汞污染的调查表明,务川汞矿区大气汞浓度为7-40000 ng·m-3,超出正常大气汞浓度1-4个数量级.地表水总汞为43-2100 ng·l-1,远高于对照区(15-29 ng·l-1);活性汞、溶解态汞和颗粒态汞含量也显著高于对照区,颗粒态汞是地表水汞迁移的主要方式.土壤总汞含量为1.3-360 mg·kg-1,远高于对照区土壤总汞含量(O.22-0.39 mg·kg-1),土壤剖面汞含量的垂向递减反映了大气汞的沉降是土壤汞的重要来源之一;同一地点不同土地利用类型的土壤,一般为稻田总汞含量高于菜地和玉米地;土壤pH值和有机质影响着土壤中汞的迁移和富集.     

贵阳市2种不同类型草地的汞释放通量

利用动态通量箱法对贵阳市人工草坪和天然草地的汞释放通量进行了野外实测. 结果表明:春季和夏季的草地是大气中汞的来源,并未出现明显的季节性变化,其平均汞释放通量为(7.8±15.7)～(41.5±15.2) ng/(m2·h),且天然草地的汞释放通量明显高于人工草坪. 草地的汞释放通量具有明显的日变化特征,白天汞释放通量显著高于夜间,最大值通常出现在午后,最小值则出现在夜间. 草地的汞释放通量与光照强度、土壤温度、大气温度呈显著的正线性关系,与大气相对湿度呈负线性关系. 大气中气态总汞的质量浓度是影响草地汞释放通量的另一个重要因素. 大气中气态总汞质量浓度的升高能够抑制草叶片向大气中释放汞,而高质量浓度的气态总汞可导致大气中的汞向草叶片的强烈沉降.      

济南市大气颗粒汞的浓度特征及污染来源解析

为了解冬季采暖对济南市大气PM_2.5中汞浓度的影响,在济南市城郊开展了为期超过两年的PM_2.5样品采集工作,共计采集有效样品481个,测定并分析其中的颗粒汞(PHg)浓度和汞含量变化特征。结果表明,济南市大气PHg在采暖期的浓度均值为583.1 pg/m³,约为非采暖期的1.4倍,在国内外城市中处于中等偏上水平。济南市大气PM_2.5对PHg具有极强的富集能力,且在采暖期更强,可能与燃煤等活动排放了更多的超细颗粒物有关。在采暖期,大气PHg浓度主要受煤炭燃烧源和交通排放源影响,两者分别贡献了总方差的39.2%和16.7%;在非采暖期,气象条件季节性变化、交通排放源、煤炭燃烧源的影响显著,三者分别贡献了总方差的32.4%、15.8%、12.0%。高浓度PHg主要来源于分布在采样站点东北偏东方向上的众多燃煤工业企业。此外,济南市大气PHg还主要受来源于鲁西南地区的区域污染气团的影响,途经污染较重的京津冀地区的污染气团对济南市PHg浓度也有较大贡献。在非采暖期,济南市PHg还受到来自东南和西南方向的清洁海洋气团的显著影响。     

同位素示踪法检测废水中TCC／TCS生物毒性的研究

用同位素示踪法测定微生物的葡萄糖摄入量,可能检测废水中有毒物质的生物毒性。实验结果显示：ＴＣＣ／ＴＣＳ对废水处理系统中厌氧菌的葡萄糖摄入有抑制作用,其抑制率与接触剂量的对数呈线性关系,但与接触时间却没有明显的线性关系。由此可见,ＴＣＣ／ＴＣＳ对微生物葡萄糖摄入的影响是复杂的。当生物处理系统中的微生物未接触ＴＣＣ／ＴＣＳ时,１０％有作用浓度（ＥＣ１０）和５０％有作用浓度（ＥＣ５０）分别为１．７１ｍｇ     

Temporal Trends in Mercury Accumulation in Lake Sediments in Sweden

Lake sediment cores were analyzedto study the history of mercury (Hg) pollution andparticularly to determine whether recent sedimentconcentrations have declined in response todeclining atmospheric deposition of Hg. Sedimentcores from 6 forest lakes distributed fromsouthern to northern Sweden and 3 northernmountain lakes were analyzed for Hg using CVAAS. A400 cm sediment profile from Måkevatten insouthwest Sweden indicates that the onset of Hgpollution occurred in the 18th century. Anindisputable increase in Hg concentrationsoccurred concurrent with the appearance ofspheroidal carbonaceous flyash particles (SCP)derived from fossil-fuel combustion, in themid-19th century. There is a strong correlationbetween Hg and SCP concentrations in the sedimentcores (r=0.67 to 0.91), which suggests a strongrelationship between historical Hg pollution andfossil fuel burning. In contrast to sediment corestaken in 1979, maximum Hg concentrations are nowobserved below the sediment surface and declinetowards the sediment surface. This study confirmsthat reductions in atmospheric deposition of Hgover Sweden have resulted in a decreased transferof total Hg to aquatic environments as reflectedby lake sediments, and that lake sediment profilesof Hg concentrations reflect relative trends inthe atmospheric deposition of Hg rather thanpost-depositional diagenetic processes.     

Mobility and Methylation of Mercury in Forest Soils Development of an In-Situ Stable Isotope Tracer Technique and Initial Results

A method for investigating in-situmethylation and mobility of mercury has beendeveloped and applied to forest soil. The methodis based on additions of stable ¹⁹⁹Hgisotopes to forest soil plots followed bysampling and analysis of isotope ratios of totalmercury and MeHg using ICP-MS. Initial resultsindicate that a fraction (30%) of the mercuryadded to the forest soils is immobilised over atime scale of 16 months. A small but significantfraction of the mercury is methylated during thesame time scale. Higher methylation rates werefound in wetland soil than in dry forest podzolsoil.