地下水补给型湖泊表层沉积物矿物组成及其形成机制——以巴丹吉林沙漠湖泊群为例

盐湖中的矿物沉积记录着丰富的环境气候变化信息,是古环境研究的重要对象.在无地表径流补给的盐湖中,其矿物组成及沉积特征与有地表径流补给的湖泊相比是否有一定的特殊性,是值得探讨的问题.采集巴丹吉林沙漠33个不同矿化度地下水补给型湖泊的表层沉积物和10个地表风积砂样品,通过X衍射的方法,分析样品的矿物组成.结果显示:湖泊表层沉积物主要为石英、长石、辉石、云母等碎屑矿物,部分湖泊含有少量的碳酸盐和氯化物盐类矿物.湖泊沉积物的矿物组成与湖水矿化度的关系较为密切,淡水湖仅分布碎屑矿物,微咸水湖含有碎屑矿物和碳酸盐类矿物,盐湖含有碎屑矿物、碳酸盐类矿物和氯化物.风积砂样品中主要为碎屑矿物,占总矿物含量的90%,对湖泊沉积物的矿物组成影响较大,但对湖泊沉积物中的盐类矿物没有贡献,表明湖泊表层沉积物中盐类矿物主要是自生作用形成的.虽然本地区湖泊边缘的沉积物中盐类矿物种类相对较少并且含量较低,但其盐类矿物组成与分布能够响应湖水矿化度的变化,其环境指示意义与有径流补给的盐湖相同,可以指示其湖水的盐度.因此,可以从巴丹吉林沙漠地下水补给型湖泊沉积的盐类矿物中提取相应的古环境信息,用于恢复古气候和古环境的研究.     

湖泊沉积物碳酸盐含量的XRD半定量分析

湖泊沉积中的碳酸盐对于气候环境具有很好的指示意义.利用化学分析方法(气量法)和X衍射(XRD)方法,对青藏高原可可西里库赛湖KS-2006孔沉积物中的碳酸盐含量进行了半定量分析.结果表明:虽然KS-2006孔沉积物中的矿物种类达9种之多,且XRD的测量误差(±5%)高于气量法的测量误差(±0.8%);但XRD法获得的KS-2006孔沉积物碳酸盐总含量的平均值(18.9%)以及波动范围(7%~39%),同气量法所获得的碳酸盐含量的平均值(19.4%)和波动范围(5.0%~30.7%)基本一致,而且二者具有很好的正相关关系(相关系数R²为0.3940),随深度的波动趋势一致,说明XRD方法在半定量分析湖泊沉积物碳酸盐矿物种类及其含量方面,具有很高的可靠性.     

近百年来洞庭湖粒度指示的沉积环境演变特征

湖泊沉积物储存着长时期的流域环境信息,是百年尺度湖泊环境演变研究的高分辨率记录器。本文通过²¹⁰Pb_ex、¹³⁷Cs组合定年法,分析放射性核素剖面特征,研究沉积速率时空变化规律,并解析沉积物粒度指示的环境信息,揭示百年尺度湖泊沉积环境演变。结果表明:洞庭湖²¹⁰ Pb_ex剖面分布呈现多段衰变型、混合—衰变—平衡型、衰变—本底型和无沉积型4种类型。3大湖体200 cm的沉积深度对应的年代跨度为127～162年,构建了洞庭湖沉积物深度—年代关系。洞庭湖平均质量沉积速率为1.47～3.11 g/(cm²·a),整体上呈现南洞庭湖>西洞庭湖>东洞庭湖的空间特征;自1900年后,质量沉积速率增加了3～7倍,呈时序增加趋势。沉积年代上,沉积物粒度特征表明洞庭湖沉积环境呈3个阶段2个过渡期的演变特征,与同时期区域内毁林开荒、水利建设、植树造林等人为活动有较好的对应关系,说明近百年来人为活动是洞庭湖泥沙沉积的重要因素。本研究结果可为强化湖泊及其流域生态环境保护...     

湖泊沉积物碳酸盐含量3种测定方法的比较

湖泊沉积物中碳酸盐含量是指示气候和环境变化的常用指标之一,其测定方法多样,但缺乏不同测定方法结果之间的比较,尤其是对同一沉积序列样品的比较.选择新疆天山大龙池DLC12孔110 cm岩芯沉积物,按1 cm间隔取样,利用烧失量法、酸碱滴定法和气量法分别进行碳酸盐含量分析,并比较3种分析方法在表达湖泊沉积物碳酸盐含量时的差异性.结果表明:3种方法测定的碳酸盐含量随岩芯深度的变化趋势并无太大差别,其中烧失量法测定的结果较滴定法和气量法测定的结果平均分别偏高5%和3%,气量法结果与滴定法结果较为接近,平均差值不到2%,表明烧失量测定过程中有其他矿物分解导致碳酸盐含量被高估.将3种方法测定的结果与岩芯中20个样品的X衍射(XRD)得到的碳酸盐含量对比,发现气量法的测定结果与XRD测定结果的相关性最高.通过比较各种方法的优缺点,考虑到分析精度、操作技巧和分析费用,认为气量法比较适合湖泊沉积物的碳酸盐含量分析.     

云南程海沉积物碳酸盐来源辨识

碳酸盐是湖泊沉积物的组成部分,其碳、氧同位素组成是恢复湖区古气候/古环境的有效代用指标.沉积物碳酸盐包括物源区带来的外源碳酸盐和湖泊内生沉淀产生的自生碳酸盐,其中只有自生碳酸盐才具有古气候指示意义.故沉积物碳酸盐来源辨识是开展碳酸盐古环境记录研究的基础和前提.通过多种方法的综合判别,证明了程海沉积物碳酸盐主要是自生碳酸盐,为开展碳酸盐记录研究提供了可靠依据.程海是开展碳酸盐碳氧同位素与古气候研究的理想场所,尤其值得深入研究.     

青藏高原苟鲁错近几十年环境变化的湖泊沉积记录

通过对青藏高原苟鲁错湖泊沉积物碳酸盐含量,粒度、C值的综合分析,得出湖泊流域气候近几十年来气候呈干暖化趋势。另外,通过苟鲁错附近五道梁和沱沱河气象站统计资料和湖泊沉积特性的对比分析,说明通过碳酸盐、粒度、C值等综合指标对重建苟鲁错流域古气候是可行的,这为苟鲁错流域古气候重建提供了参考和依据。     

艾比湖水化学演化的初步研究

本文通过野外地质调查和大量样品的分析测试结果,从以下三个方面对艾比湖湖水的水化学特征进行论述:(1)湖水的矿化度和pH;(2)湖水的化学组成;(3)湖水化学组分的侧向分布。初步揭示了湖水水化学变化和主要化学元素迁移和富集的规律。艾比湖沉积物中碳酸盐矿物组成及其地球化学性质反映湖水化学组成的变动。这种变动明显受气候环境变化的影响。因此,CK4孔和湖底沉积物中的碳酸盐沉积,提供了许多信息作为湖水化学演化和古气候波动的标志,根据其碳酸盐含量、方解石含量、方解石格架中MgCO_3mol.％、Sr含量和Sr×1000/Ca比值,最后结合碳酸盐的沉积特征、地球化学演化和古沙嘴的演变,进一步阐明了湖水化学演化的趋势。     

贵州草海沉积物碳酸盐碳同位素异常正值的发现及其环境指示意义

对贵州草海沉积物柱芯碳酸盐碳同位素组成测定的结果显示,其δ13C值的变化范围为- 14.25‰至23.10‰,变化幅度为37.35％,这是迄今所发现的湖泊沉积物碳酸盐中最大的碳同位素变化幅度,其中的部分同位素值也是迄今发现的最大碳同位素值.综合碳酸盐氧同位素、碳酸盐含量和有机质含量指标,认为草海沉积物碳酸盐碳同位素组成...     

青海湖沉积碳酸盐矿物之间氧同位素分馏的评估及其环境意义

青海湖沉积岩芯的矿物学和稳定同位素研究结果显示自生碳酸盐矿物以单种或多种矿物形式保存在沉积物中;不同碳酸盐样品的δ18O值的变化范围为5.47‰至-1.04‰,差值最高达6.5‰;δ18O值与总碳酸盐含量呈正相关关系,与碳酸盐矿物种类的改变则无明显关联.结果表明,造成δ18O显著变化的主导因素是湖水氧同位素组成,自然条件下生成的不同碳酸盐之间的氧同位素分馏不明显.说明δ18O是指示闭流湖泊降水蒸发水量平衡变化的敏感指标之一.     

137Cs质量平衡法测算青海湖现代沉积速率的尝试

本文是~(137)Cs质量平衡法测算青海湖现代沉积速率的尝试.青海湖和其他低沉积速率湖泊沉积物剖面中,深度数cm处的~(137)Cs蓄积峰,也可能是沉降到底泥表面的~(137)Cs尘埃,以扩散和迁移的方式向下入渗形成.因此,将沉积剖面中的~(137)Cs蓄积峰解释为1963年的沉积,并据此计算沉积速率,未必合理.青海湖湖滨草地测得的2005年~(137)Cs本底值为1 17.7mBq/cm~2.湖泊中部海心山到东南部渔场一线的6个孔的~(137）Cs面积活度介于92.9-325.0mBq/cm~2,其中青海湖东南部两个孔的~(137)Cs面积活度较高,分别为本底值的155%和270%;湖泊中部4个孔的~(137)Cs面积活度略高于或低于本底值.显然,湖泊东南部有明显沉积发生,特别是位于江西沟冲积扇前缘水下部分的QHH02孔,沉积强烈,水深也最小;湖泊中部沉积轻微.根据表层底泥样品的~(137)Cs浓度,入湖河流泥沙的~(137)Cs浓度和流域内草地表层土壤~(137)Cs浓度的分析,初步确定C=30mBq/g,为1963年以来青海湖沉积泥沙的平均~(137)Cs浓度.利用~(137)Cs质量平衡模型求得的湖泊中部的平均沉积速率为0.020cm/a,和根据布哈河输沙模数求算出的青海湖平均沉积速率0.018cm/a吻合,远低于已报导的断代法测定的青海湖沉积速率.湖泊东南部的沉积速率大于湖泊中部,QHH02孔的沉积速率高达0.229cm/a,是已报导的青海湖沉积速率的两倍.     

太湖沉积物的磁性特征及其环境意义

本文以太湖沉积物为研究对象,试图在磁性测量的基础上,对太湖湖区四个样芯进行分层,建立芯间层位对应联系,并结合孢粉,粒度,地球化学和有机质含量等分析测定,从沉积物样芯的磁参数曲线变化中提取该地区的环境变化信息,研究结果表明,由于该方法具快速简便,经济易行,无破坏等优点,从而可能对样芯作连续测量,以提取分辨率的环境变化信息,在湖泊沉积物的研究中有着独的作用,可作为地球化学,孢粉,微体古生物,粒度等分析     

1850年以来呼伦湖沉积物无机碳埋藏时空变化

湖泊沉积物碳埋藏及其驱动机制是陆地生态系统碳循环及全球变化研究的热点问题之一,但以往湖泊碳循环的研究大多局限于有机碳,较少考虑无机碳的地位和作用.我国干旱-半干旱地区湖泊众多、无机碳储量丰富,在区域碳循环过程中的作用日益突出,因此探讨这些地区湖泊沉积物无机碳埋藏变化对深入理解区域碳循环具有重要意义.本研究通过对内蒙古高原呼伦湖15个沉积岩芯样品无机碳含量(TIC)的测定,结合沉积岩芯210Pb、137Cs年代标尺,分析了1850年以来呼伦湖无机碳埋藏速率时空变化,并揭示了影响呼伦湖无机碳埋藏的主要因素.结果表明,1980s之前,呼伦湖无机碳含量总体维持在相对稳定的低值,1980s之后开始快速增加,且近百年来呼伦湖平均无机碳含量在不同湖区差异不显著.1850年以来呼伦湖无机碳埋藏速率变化范围约为7.10～74.29 g/(m2·a),平均值约为36.15 g/(m2·a),且大体上可分为3个阶段,即1900s以前相对稳定的低值阶段、1900s-1950s期间的快速增加阶段以及1950s以来的波动增加阶段,各阶段无机碳埋藏速率平均值分别约为10.40、26.29和41.00 g/(m2·a).空间上,呼伦湖无机碳埋藏速率整体表现为中部高、南北两端低的分布格局,这可能与湖心水动力条件相对稳定,有利于碳酸盐沉积有关.此外,呼伦湖无机碳埋藏速率与湖区温度变化呈显著正相关,而与周边人类活动影响关系不明显,表明在未来全球变暖背景下,呼伦湖无机碳埋藏速率将进一步增加,湖泊在区域碳循环中的作用将更加显著.     

太湖近代沉积物中重金属元素的累积

利用210Pb、137Cs定年技术,对来自太湖不同生态和沉积特征的三个湖区的沉积物柱状样品进行了定年,用ICP—AES分析了沉积物中重金属等元素的含量,分析了太湖沉积物中重金属的累积特征及其成因.污染较重、蓝藻水华暴发频繁的梅梁湾沉积物中的重金属含量在近25年来逐年增加;太湖上游风浪较大的夹浦湖区表层10cm沉积速率大、粒度粗,除表层1cm外,1—10cm沉积物中各种重金属含量都较低,且层间变化剧烈;下游湖区正逐渐草型化的胥口湾除表层3cm外,沉积物中重金属的含量自底层向表层大致呈不断下降的趋势.研究表明,不同年代的太湖沉积物中重金属含量差异很大,明显大于不同湖区间沉积物重金属平均含量间的差异.水动力作用引起的沉积物粒度分异很可能是影响沉积物中重金属积累的一个重要因素.总体上太湖沉积物中重金属的污染比较轻微,但已经有一定程度的Cd污染,梅梁湾沉积物中自上世纪70年代开始明显积累Cd,其他重金属元素的积累也逐渐增加,值得关注.     

Sudden enhancement of sedimentation flux of~(210)Pb_(ex) as anindicator of lake productivity as exemplified by Lake Chenghai

Recent sediments in lakes and gulfs are a sensi-tive recorder of the information about environmentalchanges in the catchment areas during recent geologi-cal history. Precise determination of the ages of sedi-ments is the key to deciphering the environmental re-cords. The 210Pb dating technique and the markertechnique based on fallout radionuclide 137Cs havefound wide applications in sedimentation rate on atime scale of several tens to one hundred years, as wellas the varve chron…     

从沉积物特征谈太湖的演变

通过太湖湖底淤泥层中的微体古生物及其物理化学分析,在西太潮W1孔发现多门类海相化石。海相化石出现的时间约在1100—5000aB.P.之间。据此提出西太湖在全新世期间曾遭受海侵,因而支持了太湖形成于泻湖的说法,同时,还提出海水进入太湖的时间,比以往学者推测的早2000多年。     

Phosphorus forms and bioavailability of lake sediments in the middle and lower reaches of Yangtze River

Forms of phosphorus in sediments from 25 lakes in the middle and lower reaches of Yangtze River were analyzed by the sequential extraction procedure. Contents and spatial distrubution of algal available phosphorus (AAP) in sediments of Lake Taihu, the third largest freshwater lake of China, were also studied. Relationships between phosphorus forms in sediment and macrophytes coverage in sample sites, as well as phosphorus forms in sediments and chlorophyal contents in lake water were discussed. Exchangeable form of phosphorus (Ex-P) in surface sediments was significantly positive correlative to total phosphorus (TP), dissolved total phosphorus (DTP) and soluble reactive phosphorus (SRP) contents in the lake water. Bioavailable phosphorus (Bio-P) contents in sediments from macrophytes dominant sites were significantly lower than that in no macrophyte sites. In Lake Taihu, Ex-P content in top 3 cm sediment was highest. However, content of ferric fraction phosphorus (Fe-P) was highest in 4–10 cm. Bioavalilble phosphorus (Bio-P) contents in surface sediments positively correlated to Chlorophyll a contents in water of Lake Taihu with significant difference. Therefore, contents of Bio-P and AAP could be acted as the indicators of risks of internal release of phosphorus in the shallow lakes. It was estimated that there were 268.6 ton AAP in top 1 cm sediments in Lake Taihu. Sediment suspension caused by strong wind-induced wave disturbance could carry plenty of AAP into water in large shallow lakes like Lake Taihu.     

太湖14000年来古环境演化的湖泊记录

Two sediment cores, one 396 cm long from west Taihu Lake, another 246 cm long from east Taihu Lake, are interpreted from the analysis of their magnetic susceptibility, total organic carbon, total nitrogen, total pigments, organic carbon isotope, hydrogen index, saturated hydrocarbons, ¹⁴C dating and surficial sediment conditions. The west Taihu Lake core is the longest one studied in this lake so far, and has provided us the most complete environmental and climatic information for this lake. The results from the west Taihu lake core indicate that Taihu Lake has undergone the following stages:from ca.14 300 to 13 300 aB.P. Taihu Lake was in low lake-level, and there existed exposed features from the proxies reflecting arid paleoclimate. From ca.13 300 to 12 400 aB.P. an arid transitional stages occurred with a slightly warmer and wetter climate. From ca. 12 400 to 10 900 aB.P. a period of large climatic fluctuation occurred and from 10900-10 000 aB.P. a warm period developed with deep water and strongly reducing sediments. During ca.10 000-7 200aB.P., a cool transitional period alternating with a warm climate occurred. It was warm and wet during 7 200-5 700aB.P.; some proxies changed violently in 5 050aB.P., reflecting obvious changes in material source and a probable interruption of sedimentation. The east Taihu Lake history from ca. 6 550 to 6 450 aBP, the climate was cold and dry, and gradually turned warm and wet in ca. 6 450-6 050 aBP. It was warm and wet in ca. 6 050-5 800 aBP and had a cold tendency in 5 800-ca. 5 000 aBP. An abrupt change occurred at ca. 5 000 aBP, and the lake sediment in the uppmost part was disturbed by wave action indicating shallow water conditions.     

Phosphorus forms and bioavailability of lake sediments in the middle and lower reaches of Yangtze River

Forms of phosphorus in sediments from 25 lakes in the middle and lower reaches of Yangtze River were analyzed by the sequential extraction procedure. Contents and spatial distrubution of algal available phosphorus (AAP) in sediments of Lake Taihu, the third largest freshwater lake of China, were also studied. Relationships between phosphorus forms in sediment and macrophytes coverage in sample sites, as well as phosphorus forms in sediments and chlorophyal contents in lake water were discussed. Exchangeable form of phosphorus (Ex-P) in surface sediments was significantly positive correlative to total phosphorus (IP), dissolved total phosphorus (DTP) and soluble reactive phosphorus (SRP) contents in the lake water. Bioavailable phosphorus (Bio-P) contents in sediments from macrophytes dominant sites were significantly lower than that in no macrophyte sites. In Lake Taihu, Ex-P content in top 3 cm sediment was highest. However, content of ferric fraction phosphorus (Fe-P) was highest in 4 - 10 cm. Bioavalilble phosphorus (Bio-P) contents in surface sediments positively correlated to Chlorophyll a contents in water of Lake Taihu with significant difference. Therefore, contents of Bio-P and AAP could be acted as the indicators of risks of internal release of phosphorus in the shallow lakes. It was estimated that there were 268.6 ton AAP in top 1 cm sediments in Lake Taihu. Sediment suspension caused by strong wind-induced wave disturbance could carry plenty of AAP into water in large shallow lakes like Lake Taihu.     

Effect of mining and related activities on the sediment trace element geochemistry of Lake Coeur D'Alene,Idaho, USA part II: Subsurface sediments

During the summer of 1990, 12 gravity cores were collected in Lake Coeur d'Alene, Idaho at various depths and in a variety of depositional environments. All core subsamples were analysed to determine the bulk sediment chemistry; selected subsamples were analysed for trace element partitioning and ¹³⁷Cs activity. The purpose of these analyses was to determine the trace element concentrations and distributions in the sediment column and to try to establish a trace element geochemical history of the lake in relation to mining and mining-related discharge operations in the area. Substantial portions of the near-surface sediments in Lake Coeur d'Alene are markedly enriched in Ag, As, Cd, Hg, Pb, Sb and Zn, and slightly enriched in Cu, Fe and Mn. Variations in the thickness of the trace element-rich sediments, which range from more than 119 cm to as little as 17 cm, indicate that the source of much of this material is the Coeur d'Alene River. An estimated 75 million tonnes of trace element-rich sediments have been deposited on or in the lake bed. Estimated trace element masses in excess of those considered representative of background conditions range from a high of 468 000 tonnes of Pb to a low of 260 tonnes of Hg. The similarity between the trace element-rich surface and subsurface sediments with respect to their location, their bulk chemistry, their interelement relations and their trace element partitioning indicate that the sources and/or concentrating mechanisms causing the trace element enrichment in the lake sediments have probably been the same through-out their depositional history. Based on a Mt St Helens'ash layer from the 1980 eruption, ages estimated from ¹³⁷Cs activity and the presence of 80 discernible and presumably annual layers in a core collected near the Coeur d'Alene River delta indicate that deposition rates for the trace element-rich sediments have ranges from 2.1 to 1.3 cm/year. These data also indicate that the deposition of trace element-rich sediments began, at least in the Coeur d'Alene River delta, some time between 1895 and 1910, dates consistent with the onset of mining and ore processing activities that began in the area in the 1880s.