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.     

The effect of mining and related activities on the sediment–trace element geochemistry of Lake Coeur d'Alene,Idaho, USA. Part III. Downstream effects: the Spokane River Basin

During 1998/1999, surface and subsurface sediment samples were collected along the entire length of the Spokane River from its outlet at the northern end of Lake Coeur d'Alene (CDA), Idaho, to Lake Roosevelt on the Columbia River, Washington. The study was conducted to determine if the trace element enrichments observed in Lake CDA and on the floodplain and in the CDA River extend through the Spokane River Basin (SRB). As in Lake CDA, surface sediments in the SRB are enriched in Pb, Zn, As, Cd, Sb and Hg relative to local background levels. Pb, Cd and Zn are the most elevated, with maximum enrichment occurring in the upper Spokane River in close proximity to Lake CDA. On average, enrichment decreases downstream, apparently reflecting both increased distance from the inferred source (the CDA River Basin), as well as increased dilution by locally derived but unenriched materials. Only Cd and Zn display marked enrichment throughout the SRB. Pb, Zn and Cd seem to be associated mainly with an operationally defined iron oxide phase, whereas the majority of the As and Sb seem to be matrix‐held. Subsurface sediments also are enriched in Pb, Zn, As, Cd, Sb and Hg relative to background levels. Based on ¹³⁷Cs and excess ²¹⁰Pb dating, trace element enrichment began in the middle part of the SRB (Long Lake) between 1900 and 1920. This is contemporaneous with similar enrichments observed in Lake CDA, as well as the completion of Long Lake Dam (1913). In the most downstream part of the basin (Spokane River Arm of Lake Roosevelt), enrichment began substantially later, between 1930 and 1940. The temporal difference in enrichment between Long Lake and the River Arm may reflect the latter's greater distance from the presumed source of the enrichment (the CDA River Basin); however, the difference is more likely the result of the completion of Grand Coulee Dam (1934–1941), which formed Lake Roosevelt, backed up the Spokane River, and increased water levels in the River Arm by about 30 m.     

柴达木盆地苏干湖表层沉积与尘暴事件——元素示踪的初步结果

通过分析苏干湖地区10个地表表层沉积物、9个大气降尘(含2个尘暴降尘)、16个湖泊表层沉积物等样品的8种常量-微量元素和11种稀土元素的含量,以及同类沉积不同元素含量和不同沉积同一元素含量的相关性,结果表明,在湖泊沉积体系中Al、Fe、Sc含量的变化与强风-尘暴过程有关,指示了湖泊沉积碎屑颗粒风成输入的可能性．元素Fe、Sc含量在3种不同的沉积物中差异不大,与尘暴事件的强度和频次有关．稀土元素结果显示3类沉积具有同源性．苏干湖沉积可以用来重建研究区尘暴演化历史．     

Hydrological response to timber harvest in northern Idaho: implications for channel scour and persistence of salmonids

The potential for forest harvest to increase snowmelt rates in maritime snow climates is well recognized. However, questions still exist about the magnitude of peak flow increases in basins larger than 10 km² and the geomorphic and biological consequences of these changes. In this study, we used observations from two nearly adjacent small basins (13 and 30 km²) in the Coeur d'Alene River basin, one with recent, relatively extensive, timber harvest, and the other with little disturbance in the last 50 years to explore changes in peak flows due to timber harvest and their potential effects on fish. Peak discharge was computed for a specific rain‐on‐snow event using a series of physical models that linked predicted values of snowmelt input to a runoff‐routing model. Predictions indicate that timber harvest caused a 25% increase in the peak flow of the modelled event and increased the frequency of events of this magnitude from a 9‐year recurrence interval to a 3·6‐year event. These changes in hydrologic regime, with larger discharges at shorter recurrence intervals, are predicted to increase the depth and frequency of streambed scour, causing up to 15% added mortality of bull trout (Salvelinus confluentus) embryos. Mortality from increased scour, although not catastrophic, may have contributed to the extirpation of this species from the Coeur d'Alene basin, given the widespread timber harvest that occurred in this region. Copyright © 2008 John Wiley & Sons, Ltd.     

Dynamics of dissolved major (Na,K, Ca,Mg, and Si) and trace (Al,Fe, Mn,Zn, Cu,and Cr) elements along the lower Orinoco River

This study addresses the changes in dissolved major and trace element concentrations along the Orinoco River, including the mixing zone between the Orinoco and Apure Rivers. Water samples from the Apure and Orinoco Rivers were collected monthly in four sectors over a period of 15 months. Auxiliary parameters (pH, dissolved oxygen, conductivity, and temperature), total suspended sediments, dissolved organic carbon (DOC), and major (Na, K, Ca, Mg, and Si) and trace (Al, Fe, Mn, Zn, Cu, and Cr) element concentrations were measured in all sectors. The relative contribution of both rivers after the Apure–Orinoco confluence was determined using Ca as a tracer. Moreover, a mixing model was developed to determine whether dissolved species exhibit a conservative behavior during mixing. The results indicate that DOC is removed from waters during the Apure–Orinoco mixing, probably due to absorption of DOC on mineral phases supplied by the Apure River. Dissolved Na, Ca, and Mg behave conservatively during the mixing processes, and their concentrations are controlled by a dilution process. The anomaly in the temporal pattern of K in the Orinoco is caused by the input of biogenic K originating from the Apure River during the high‐water stage. The loss of dissolved Si during the low‐water stage can be explained by the uptake of Si by diatoms. Dissolved Mn, Zn, Al, and Fe showed a non‐conservative behavior during the Apure–Orinoco mixing. The removal of Mn and Zn from the dissolved phase can be explained by the formation of Mn‐oxyhydroxides and the scavenging of Zn onto Mn oxides. Dissolved Fe is controlled by redox processes, although the removals of Fe and Al due to the preferential adsorption of large organometallic complexes by mineral surfaces after the Apure–Orinoco confluence can affect the mobility of both elements during transport. The conservative behavior shown by Cu and Cr can be related to the tendency of both elements to be complexed with small organic colloids, which are not preferentially adsorbed by clays.     

长江中游湖泊表层沉积物多环芳烃的分布、来源特征及其生态风险评价

为明确长江中游地区湖泊沉积物中多环芳烃（PAHs）的分布特征、来源及其生态风险,于2018年7月采集了该地区12个湖泊的表层沉积物样品.采用气相色谱-质谱联用仪（GC-MS）测定了沉积物中16种PAHs的含量.结果表明：12个湖泊沉积物中均检测出16种优控PAHs,PAHs的总含量在572.7~1766.2 ng/g （dw）之间（均值为976.5±285.0 ng/g （dw））.武汉市东湖沉积物中PAHs含量最高,达到1634.8±111.4 ng/g （dw）.与国内外其他地区湖泊沉积物相比,长江中游地区湖泊沉积物中PAHs含量高于国内偏远地区的抚仙湖、青海湖及博斯腾湖,低于东部地区的巢湖、太湖及美国经济工业发达地区的湖泊.根据单体PAH的聚类分析结果,12个湖泊可以分成3种类型,类型1主要以低环为主,占比为64.04%±7.02%,类型2低环和中高环分布相对平均,分别为50.76%±5.17%和49.24%±5.17%,类型3低、中、高环分布相对平均,占比分别为35.35%±3.56%、26.17%±0.45%和38.48%±3.84%.综合该区域PAHs的分布特征及异构体比值法与主成分分析法的结果表明,类型1湖泊沉积物中PAHs主要来源为煤炭、木材等生物质的燃烧源;类型2和类型3湖泊沉积物中PAHs主要来源为煤炭、木材等生物质的低温燃烧以及机动车等燃烧汽油、柴油的尾气排放和工业炼焦等化石燃料的高温燃烧源.沉积物中PAHs与总有机碳（TOC）之间显著的相关性表明,沉积物中TOC含量是影响长江中游湖泊沉积物中PAHs归趋分布的主要因素.长江中游流域湖泊沉积物中PAHs的RQ_NCs值均小于800,且RQ_MPCs值大于1的风险商值法生态风险评价结果表明,长江中游流域湖泊表层沉积物中PAHs整体呈中等风险水平.     

黄河下游南四湖地区黄河河道变迁的湖泊沉积响应

黄河下游地区湖泊演化多与黄河河道变迁密切相关,进行高分辨率的湖泊沉积环境的研究,可揭示历史时期黄河下游的河道变迁,本文以南四湖ＤＳ孔为例,探讨河道变迁的湖泊沉响应。     

云南腾冲青海——酸性湖泊的环境特征

火山口湖成因和持续酸性地下水补给是腾冲青海呈现酸性湖泊环境的地质基础,通过对青海环境的实际调查和水、土、生物样品的分析、鉴定,结果表明：湖水具较低pH值、极低的阳离子组成和矿化度;沉积物中Ca、Mg、Al、Fe等元素有明显流失;湖泊生物种群少且生物量低,缺失蓝藻和腹足类、瓣鳃类、甲壳类动物等为区别于一般中、碱性湖泊最显著的特点,酸性水介质湖泊系统元素地球化学行为的变化及其对生物的影响－－生物贫化和耐酸种扩张,既是腾冲青海的基本特点,也是酸性湖泊环境形成的动力机制。     

内蒙古呼伦湖表层沉积物的矿物组成和沉积速率

呼伦湖表层沉积物的取样和分析表明,沉积物主要由碎屑矿物和自生碳酸盐矿物组成。碳酸盐含量为10％—18％。碳酸盐沉积作用与湖水的较高含盐量和碳酸盐过饱和度有关。湖泊中心HL8号柱样的~(210)Pb测定结果是,10cm以上平均沉积速率0.25cm/a,10—12cm为0.05cm/a。60年代开始随湖泊水位上涨沉积物输入量迅速加大。     

Mineralogical signatures and sources of recent sediment in a large tropical lake

Two lead-210 (²¹⁰Pb) dated sediment cores from Chapala Lake were studied to identify the mineral composition of the sediments and to discuss its relation with trace metals. Minerals and trace metals reflected the domain of volcanic rocks (i.e. basalts, rhyolite and andesite) that characterize Chapala Lake and the Lerma River watershed. Redundancy analyses (RDA) were used to identify the sedimentary variables (magnetic susceptibility, organic matter, sand content, and mineral composition) that could be related to elemental composition. Despite the distance between the two cores (7.3 km) and hydrodynamic circulation the RDA showed that the main mechanism that controls the input of mineral species, and, therefore, element distributions in the lacustrine sediment of Chapala Lake, is related to the weathering of volcanic rocks in the Lerma-Chapala watershed, the consequent runoff and transport of fine grained catchment materials, and later in-lake processes. These findings highlight the importance of controlling watershed erosion to contribute to the improvement of the environmental quality of the lake.     

湖北梁子湖近百年来环境演变历史及驱动因素分析

湖泊生态系统的修复必须建立在历史生态环境演化过程与驱动机制认识的基础之上.针对草型湖泊演化历史研究相对不足的现状,以长江中游典型草型湖泊梁子湖为研究对象,结合210Pb和137Cs年代测试,通过对沉积柱高分辨率的多指标分析(硅藻、元素地球化学和粒度)以及流域历史资料重建近百年来梁子湖生态环境的演化过程,并在此基础上利用冗余分析定量区分影响该湖泊生态环境演化的关键驱动因子.结果显示,沉积物总磷和重金属元素Cu是影响该湖泊生态环境演化的2个显著变量,它们分别单独解释硅藻组合的12.7%和8.5%变率.这表明近百年来人类活动引起的营养输入对梁子湖生态环境演化起关键性作用,而重金属污染也是影响梁子湖环境演变的重要因子.本研究结果可以为梁子湖及长江中下游其他类似湖泊的环境治理提供科学依据.     

Salsvatn,a lake with old sea water

Salsvatn is a 464 m deep lake laying 16 m above sea level in North Trøndelag, Norway. The lake was isolated from the sea some 3,000 years ago. It is assumed that salt-water in the deepest 50 m of the lake is the remain of sea water being trapped in the lake at this time. The concentration of cloride in the salt-water layer corresponds to a salinity of 29‰ in ordinary sea water. Hydrography of the lake and changes in some components of the salt water compared with ordinary sea water are discussed. Comparison is made with changes in the stagnant layers of the Black Sea and Lake Rørholtjorden. The latest is another lake with old sea-water at its bottom. Surface sediment samples have been collected from the freshwater and salt-water layers in Lake Rørholtfjorden and from the salt-water layer of Lake Salsvatn. Some chemical components of the sediments and interstitial water have been analysed and discussed.     

Trace element contamination in the estuarine sediments along Tuticorin coast – Gulf of Mannar,southeast coast of India

Sediment samples were collected from Kallar, Korampallam creek and Punnakayal estuaries of Tuticorin coast for assessing the level of contamination by trace elements in these estuarine sediments. The trace element concentration, calcium carbonate, organic carbon and mercury level were analyzed by Inductively Coupled Plasma Atomic Emission Spectrophotometer, Titrimetric method and SnCl₂ reduction method. The results reveals that the enrichment factor, metal pollution index and geo-accumulation index of these estuarine sediments were predominantly polluted by Cd, As, Zn, Hg and Pb. The factor analysis revealed the source of trace element accumulation in the estuarine sediments particularly Mn and Fe are from riverine inputs and As and Hg from untreated industrial effluents. Among the selected estuaries, Korampallam creek was found to be highly contaminated by trace elements due to the discharge of effluents from thermal power plant, Tuticorin alkali chemicals, copper smelting, Petrochemical industries and shipping activities.     

Geochemical evidence of hydrothermal recharge in Lake Baringo,central Kenya Rift Valley

Lake Baringo, a freshwater lake in the central Kenya Rift Valley, is fed by perennial and ephemeral rivers, direct rainfall, and hot springs on Ol Kokwe Island near the centre of the lake. The lake has no surface outlet, but despite high evaporation rates it maintains dilute waters by subsurface seepage through permeable sediments and faulted lavas. New geochemical analyses (major ions, trace elements) of the river, lake, and hot spring waters and the suspended sediments have been made to determine the main controls of lake water quality. The results show that evaporative concentration and the binary mixing between two end members (rivers and thermal waters) can explain the hydrochemistry of the lake waters. Two zones are recognized from water composition. The southern part of the lake near sites of perennial river inflow is weakly influenced by evaporation, has low total dissolved species (TDS), and has a seasonally variable load of mainly detrital suspended sediments. In contrast, waters of the northern part of the lake show evidence for strong evaporation (TDS of up to eight times inflow). Authigenic clay minerals and calcite may be precipitating from those more concentrated fluids. The subaerial hot‐spring waters have a distinctive chemistry and are enriched in some elements that are also present in the lake water. Comparison of the chemical composition of the inflowing surface waters and lake water shows (1) an enrichment of some species (HCO₃^?, Cl, SO₄^2?, F, Na, B, V, Cr, As, Mo, Ba and U) in the lake, (2) a depletion in SiO₂ in the lake, and (3) a possible hydrothermal origin for most F. The rare earth element distribution and the F/Cl and Na/Cl ratios give valuable information on the rate of mixing of the river and hydrothermal fluids in the lake water. Calculations imply that thermal fluids may be seeping upward locally into the lake through grid‐faulted lavas, particularly south of Ol Kokwe Island. Copyright © 2006 John Wiley & Sons, Ltd.     

In-channel surficial fine-grained sediment laminae. Part II: Chemical characteristics and implications for contaminant transport in fluvial systems

Samples of surficial fine-grained laminae (SFGL) were collected in three south-western Ontario rivers. Each sediment sample was subjected to a sequential extraction procedure designed to partition particulate metals (Cd, Pb, Cu, Zn) into five operationally defined fractions: (1) exchangeable; (2) bound to carbonates; (3) bound to Fe-Mn oxides; (4) bound to organic matter; and (5) residual. Particulate phosphus was sequentially extracted from the sediment samples into three fractions: (1) non-apatite inorganic P; (2) apatite P; and (3) organic P. The major accumulate phases of trace metals in SFGL are carbonates, Fe-Mn oxides and organic matter. The content of NAIP in SFGL ranged from 17 to 38% of total particulate P. Compared with suspended and bed sediments, levels of P and trace metals in SFGL were lower at the study sites. A conceptual overview of physical, chemical and biological processes influencing formation of SFGL and the potential role of this fine-grained sediment for contaminant transport in fluvial systems is presented.     

湖泊沉积物中元素相态的连续提取分析—以岱海为例

如何利用湖泊/海洋沉积物地球化学代用指标有效地指示环境很大程度取决于元素的来源及其在沉积物中赋存形态的确定.对位于半干旱区的内蒙古岱海14个沉积物样品的连续提取实验及18个元素在水可溶态、可交换态、碳酸盐结合态、铁锰氧化物结合态、有机物结合态及残留态等六种赋存相态中含量变化进行了测试和研究,结合沉积物的矿物组成,结果表明在岱海流域内只经历了较弱的化学风化过程,除了Ca和Sr外,其他元素主要赋存于残留态中,只发生了很小程度的活化溶解.受元素亲合性和湖水物理化学状态的制约,出溶的Sr与Ca的赋存相态基本一致,而出溶的Pb、Be、Co、Cu、K、Mn、Fe等元素则与自生碳酸盐、有机质表现出一定的亲合性.元素在不同赋存相态中分布为地球化学环境代用指标的提取和解释提供了机理性的实验依据.     

鄱阳湖湿地土壤中Fe、Mn的迁移特征及其与水位周期变动的关系

对鄱阳湖地区蚌湖水下沉积物、滩地草甸土柱状样品不同深度土壤的酸度、氧化还原电位进行了现场测定;对剖面各层次的Ｆｅ、Ｍｎ总量,还原性Ｆｅ、Ｍｎ含量,以及有机质等进行了分析。实验表明：鄱阳湖湿地土壤中Ｆｅ、Ｍｎ有其独特的分布规律和迁移特征。元素Ｆｅ仅在水土界面轻微富集,Ｍｎ则向界面和深层双向富集;还原性Ｆｅ、Ｍｎ受氧化还原边界层的控制呈垂向分布。另外,元素Ｆｅ、Ｍｎ的水平迁移与水位变动相关,退水时Ｆｅ     

VCS柱状采样及其在中国太湖富营养化评价中的应用

The lake sediments, especially in recent years, genuinely record human being''s activities upon the lake environment. The top 30cm sections are of significance in the process of advanced cultural eutrophication and water quality deterioration. Based on the data of 4 core sam-ples obtained in June 19-22, 1997, with VCS in northern, western and southern Taihu Lake, some preliminary results are reported. Further analyses on the physico-chemical items as well as element content may reveal more information of the accelerating cultural eutrophication.     

Core Sediments from Lake Brollus (Bahra el Burullus), Egypt

Nine short cores were taken from different regions of Lake Brollus, an Egyptian large shallow brackish-water Delta lake connected with the Mediterranean Sea. The core samples were subjected to some investigations in order to know the vertical variations in the values of different constituents of the deposits. The variations of water content of the sediments are mainly due to the nature and type of these sediments. An inverse relation was found between the density of wet mud and the water content of some core samples. The sediments of the lower parts of the cores taken from the central region of Lake Brollus were enriched with organic matter and black in color. These black sediments may be remains of dense land vegetation entered into Lake Brollus by drainage and fresh water. They may be also remains of massive plankton organisms which survived for a long period in this lake under favourable conditions. The amounts of diatom-silica estimated from the sediments can be used as a rough indicator for the amounts of diatoms which were found in the lake at the time of deposition. The allochthonous materials, the organic matter, the calcareous substances and the diatomsilica generally were deposited in variable amounts at various depths of the cores. The quantitative distribution of these components in the core sediments was found to depend mainly upon certain factors which were discussed.     

Spatial and temporal heterogeneity of Lake Lugano sediment composition

The concentrations of eighteen elements (Al, C, Ca, Cd, Cr, Cu, Fe, K, Mg, Mn, N, Ni, P, Pb, S, Si, Ti, and Zn) in 76 sediment samples collected in Lake Lugano in 1973 and in 83 samples collected in 1985 were measured and used to draw distribution maps. The chemical compositions of sediments from the three lake subbasins were statistically compared, and used to describe the state of the lake at two time-points twelve years apart. The results obtained seem to be consistent with the available information about the recent evolution of Lake Lugano; both phosphorus and nitrogen are statistically higher in the 1985 samples than in those of 1973, confirming the reported tendency of the lake to evolve towards higher trophic conditions in this period of time. For both metals and mobile elements, the differences between the two sampling years and the literature data reflect fluctuations in the normal geochemical supply from the catchment basin, rather than significant contamination phenomena. However, elements like Ni, Cr, Zn, Pb and Cu tend to be more abundant in the most recent layers of the sediments, so further studies are needed to assess whether potentially hazardous conditions will evolve in the future.The work was performed at the EEC — Environment Institute, Joint Research Centre, I-21020 Ispra (Varese) Italy