武汉月湖水体和表层沉积物中25种半挥发性有机污染物分布特性

2006年4月在武汉月湖采集了8个样点的水样和表层沉积物样品,采用气-质联用技术分析了样品中25种半挥发性有机污染物(SVOCs)的含量,探讨月湖受有机物污染的程度.水样中25种半挥发性有机污染物总浓度为564.04-1209.41ng/L,平均值为965.64ng/L.沉积物中总浓度为8500.26-23347.20ng/g(DW),平均值为14832.04ng/g(DW).邻苯二甲酸酯类物质是月湖的主要污染物,其中,邻苯二甲酸乙基己基酯和邻苯二甲酸二丁酯含量最高.多环芳烃、硝基甲苯、异佛尔酮等均有不同程度检出,靠近以前的排污口的样点浓度最高.沉积物中25种半挥发性有机污染物的含量大约是水体中含量的15倍,具有潜在生态风险.     

河北西大洋水库沉积物中多环芳烃的分布、来源及生态风险评价

分析了河北西大洋水库沉积物中16种多环芳烃的含量及分布状况,并对其来源和生态风险进行了分析和评估.结果表明,表层沉积物多环芳烃总含量范围在422.36 - 1052.90 ng/g之间,且由库区上游到坝前逐渐升高.水库剖面沉积物中多环芳烃总含量在388.81 - 1205.56 ng,/g之间,自底层20 cm到表层多...     

太湖梅梁湾水体及沉积物中微囊藻毒素含量垂向分布特征

为探究太湖梅梁湾水体及沉积物中微囊藻毒素（MC-LR、MC-RR、MC-YR）含量的垂向分布特征,于2018年5月采集梅梁湾6个点位表层水、上覆水、混合水、间隙水以及柱状沉积物样品,并采用超高效液相色谱-串联质谱法分析样品中微囊藻毒素的含量.分析结果表明：水体中（表层水、上覆水、混合水以及间隙水）MC-LR、MC-RR、MC-YR的浓度范围分别为11.80~1297.14、2.50~818.40、1.80~176.00 ng/L,表层水、上覆水以及混合水中MC-LR的浓度高于MC-RR和MC-YR,MC-RR和MC-YR之间差别较小,而间隙水中MCs三种异构体浓度大小顺序为：MC-LR > MC-RR > MC-YR;垂向分布上,间隙水中MCs异构体（MC-LR、MC-RR、MC-YR）浓度均远高于表层水、上覆水以及混合水,表层水MCs异构体浓度略高于上覆水,混合水MCs异构体浓度介于表层水和上覆水之间.对沉积物的研究发现,1~10 cm表层沉积物中MC-LR、MC-RR、MC-YR含量范围分别为0.60~26.95、0~0.90、0~8.10 ng/g,且1~10 cm层中MCs三种异构体平均含量大小顺序为：MC-LR > MC-YR > MC-RR,其中MC-LR、MC-RR、MC-YR的检出率分别为100%、70%、92%;垂向分布上,MC-RR含量较低且变化不大,而MC-YR和MC-LR含量均随沉积物深度的增加先升高后降低.相关性分析结果表明,表层水和混合水中MCs与总磷浓度呈显著正相关,而与总氮浓度无显著相关性;上覆水、间隙水以及沉积物中MCs与总氮、总磷浓度均呈显著正相关.     

Perfluorinated alkyl acids in water, sediment and wildlife from Sydney Harbour and surroundings

Perfluorinated alkyl compounds (PFCs) including perfluorooctane sulphonate (PFOS) and perfluorooctanoate (PFOA) were measured in environmental samples collected from around Homebush Bay, an urban/industrial area in the upper reaches of Sydney Harbour and Parramatta River estuary. Water, surface sediment, Sea Mullet (Mugil cephalus), Sydney Rock Oyster (Saccostrea commercialis) and eggs of two bird species; White Ibis (Threskiornis molucca), and Silver Gull (Larus novaehollandiae) were analysed. In most samples PFOS was the dominant PFC. Geometric mean PFOS concentrations were 33 ng/g ww (wet weight) in gull eggs, 34 ng/g ww in ibis eggs, and 1.8 ng/g ww and 66 ng/g ww in Sea Mullet muscle and liver, respectively. In sediment the PFOS geometric mean was 1.5 ng/g, in water average PFOS and PFOA concentrations ranged from 7.5 to 21 ng/L and 4.2 to 6.4 ng/L, respectively. In oysters perfluorododecanoic acid was most abundant, with a geometric mean of 2.5 ng/g ww.     

巢湖表层沉积物中多环芳烃分布特征及来源

于2010年,采用野外采样调查、色谱分析与统计比较的方法,研究巢湖表层沉积物中27个采样点中多环芳烃(PAHs)分布特征及污染来源.结果表明:巢湖表层沉积物中检测出的14种优控PAHs总浓度为116.0~2832.2 ng/g(DW),平均值为898.9±791.0 ng/g(DW).多环芳烃组成主要以5~6环PAHs为主,占总量的32%~58%.沉积物中总有机碳含量与PAHs总量呈现良好相关性.利用蒽/(蒽+菲)与苯并[a]蒽/(苯并[a]蒽+屈)比值法对PAHs来源进行解析得出,巢湖表层沉积物中PAHs主要来源为燃烧源.与国内其它水体PAHs含量对比表明,巢湖沉积物中PAHs污染处于中等水平.生态风险评估得出南淝河表层沉积物中PAHs存在生态风险,其它采样点表层沉积物中PAHs生态风险均较低.     

The source and fate of sediment and mercury in Hunza River basin,Northern Areas,Pakistan

This article presents results of mercury in surface waters from Hunza River basin, Northern Areas, Pakistan. Small‐scale gold mining activities along the Hunza and Gilgit rivers are long known to be discharging mercury in the amalgamation and roasting processes. Previous studies reported high mercury concentrations in soils close to mining operations as well as serious health problems for miners. However, none of the studies have focused on the level of contamination in aqueous environments. This is the first study on the investigation of source and fate of sediment and river‐borne mercury in the Hunza River. The samples collected near gold panning sites showed higher mercury concentrations than critical levels established by the U.S. Environmental Protection Agency. The observed dissolved mercury concentrations ranged from 5.10 to 25.25 ng/l, whereas particulate‐bound mercury ranged from 4.85 to 154.62 ng/l. Particulate‐phase mercury corresponded to more than 75% of the total observed mercury concentrations for all of the sampled rivers. Thus, suspended sediments represented the major pathway of the riverine mercury transport. A mass balance calculation suggested an annual mercury flux of 48.6 g/km² into the Hunza River basin. The samples collected from the most affected river, the Shimsal River, averaged to have 108 ng/l total mercury. This amount was close to the average soil mercury data of 151 ng/l as reported by the Pakistan Mineral Development Corporation in 2001. The dominant source of contamination was shown to be the leaching of large quantities of mercury from the mercury‐rich sediment and flood plain soil into the rivers, rather than the direct release from mining activities. Significant decrease in both dissolved and particulate‐bound mercury concentration downstream of Attabad Lake suggested that mercury is being accumulated or consumed in the lake. Although minimization or elimination of mercury loses from the mining process seems important for the well‐being of the miners, preventing the remobilization of accumulated mercury is equally important in mercury control in this region. Copyright © 2014 John Wiley & Sons, Ltd.     

Laboratory analyses of nutrient release processes from Haihe River sediment

Sediment samples were collected from the heavily contaminated Haihe River to conduct static nutrient release experiments with tap water,and to evaluate the effect of dredging depths,salinity and light ...     

TEMPORAL AND SPATIAL DYNAMICS OF DIFFERENT PARTICLE SIZE OF SUSPENDED SEDIMENT IN THE LIU RIVER CATCHMENTS,CHINA

1 INTRODUCTION The particle size of sediment eroded from basins can provide basic information about erosion processes (Meyer et al., 1980), which can be divided into sheet wash sediment processes on hill slopes and fluvial sediment processes in rivers. In…     

Trace contaminant concentrations in the Kara Sea and its adjacent rivers, Russia.

Trace organic (chlorinated pesticides, PCBs, PAHs and dioxins/furans) and trace metal concentrations were measured in surficial sediment and biological tissues (i.e., worms, crustaceans, bivalve molluscs, and fish livers) collected from the Russian Arctic. Total DDT, chlordane, PCB and PAH concentrations ranged from ND to 1.2, ND to <0.1, ND to 1.5 and <20-810 ng g(-1), respectively, in a suite of 40 surficial sediment samples from the Kara Sea and the adjacent Ob and Yenisey Rivers. High sedimentary concentrations of contaminants were found in the lower part of the Yenisey River below the salt wedge. Total dioxins/furans were analysed in a subset of 20 sediment samples and ranged from 1.4 to 410 pg g(-1). The highest trace organic contaminant concentrations were found in organisms, particularly fish livers. Concentrations as high as 89 ng g(-1) chlordane; 1010 ng g(-1) total DDTs; 460 ng g(-1) total PCBs; and 1110 ng g(-1) total PAH, were detected. A subset of 11 tissue samples was analysed for dioxins and furans with total concentrations ranging from 12 to 61 pg g(-1). Concentrations of many trace organic and metal contaminants in the Kara Sea appear to originate from riverine sources and atmospheric transport from more temperate areas. Most organic contaminant concentrations in sediments were low; however, contaminants are being concentrated in organisms and may pose a health hazard for inhabitants of coastal villages.     

Assessment of suspended sediment transport in four alpine watersheds (France): influence of the climatic regime

High‐frequency water discharge and suspended sediment concentration (SSC) databases were collected for 3 years on four contrasted watersheds: the Asse and the Bléone (two Mediterranean rainfall regime watersheds) and the Romanche and the Ferrand (two rainfall–snowmelt regime watersheds). SSCs were calculated from turbidity recordings (1‐h time step), converted into SSC values. The rating curve was calculated by means of simultaneous SSC measurement taken by water sampling and turbidity recording. Violent storms during springtime and autumn were responsible for suspended sediment transport on the Asse and the Bléone rivers. On the Ferrand and the Romanche, a large share of suspended sediment transport was also caused by local storms, but 30% of annual fluxes results from snowmelt or icemelt which occurred from April to October. On each watershed, SSC up to 50 g l^?1 were observed. Annual specific fluxes ranged from 450 to 800 t km^?2 year^?1 and 40–80% of annual suspended sediment fluxes occurred within 2% of the time. These general indicators clearly demonstrate the intensity of suspended sediment transport on these types of watersheds. Suspended sediment fluxes proved to be highly variable at the annual scale (inter‐annual variability of specific fluxes) as well as at the event scale (through a hysteresis loop in the SSC/Q relationship) on these watersheds. In both cases, water discharge and precipitations were the main processes involved in suspended sediment production and transport. The temporal and spatial variability of hydro‐meteorological processes on the watershed provides a better understanding of suspended sediment dynamics. Copyright © 2009 John Wiley & Sons, Ltd.     

千岛湖表层沉积物中有机氯农药的残留特征及生态风险评价

对千岛湖表层沉积物中21种有机氯农药(OCPs)的残留现状进行调查,明确HCHs与DDTs的组成特征及源解析,并评估其生态风险.结果表明,千岛湖表层沉积物中共检出12种OCPs,各采样点位OCPs总量的浓度范围在0.43~12.70 ng/g之间,平均值为5.28±4.84 ng/g,处于低残留水平,其中DDTs是主要的残留物,街口、大坝前点位样品出现OCPs高残留.工业DDTs的历史使用是千岛湖表层沉积物DDTs残留的主要来源,仅街口点位样品存在林丹的污染并有新的DDTs输入,应引起重视.利用沉积物质量基准法、沉积物质量标准法分别对千岛湖表层沉积物中OCPs的生态风险进行评价,结果表明部分点位样品中OCPs的残留现状对该区生物可能存在生态风险.     

Organochlorine pesticides and PCB residues in sediments of Alexandria Harbour,Egypt

Persistent organochlorine compound concentrations were determined for 23 surface sediment samples collected from Alexandria Harbor, Egypt. Total PCB concentrations ranged from 0.9 to 1210 ng/g with four to seven Cl-substituted biphenyls being the most prevalent PCBs congeners. Different PCB congener distribution patterns were observed, probably reflecting different inputs and attenuation at various locations. Total DDT concentrations varied from <0.25 ng/g to 885 ng/g. The ratios of DDTs (2,4^′- and 4,4^′-DDT)/total DDTs (DDTs plus metabolites) in sediment samples from certain sites were 0.86 or higher, indicating little attenuation or recent input of DDT. Total chlordane (the sum of heptachlor and its epoxide, oxy-, γ- and -chlordane and cis+trans-nonachlor) ranged from <0.25 to 44 ng/g with the highest concentration found in the Arsenal Basin. The geographic distributions of PCBs, total DDTs and total chlordane were similar. Chlorinated benzenes (CBs), hexachlorocyclohexanes (HCHs), aldrin, dieldrin, endrin, chloropyrifos, endosulfan, mirex and pentachloroanisole were below detection limits or detected at low concentrations in most of the samples. Sites that were contaminated with high concentrations of organochlorine compounds were associated with dense population and low energy environment. The contamination levels of PCBs, total DDTs and total chlordane were in high range compared to other locations worldwide.     

Hydraulic and geochemical interactions between surface water and sediment pore water in seasonal hypersaline Maharlu Lake,Iran

Study of interactions between surface-water and pore-water in lakes is complicated due to spatio-temporal heterogeneities in flow condition across the sediment–water interface. In this study, seasonal hypersaline Maharlu Lake was investigated by collecting surface-water and pore-water samples from four nests of multilevel piezometers installed at different distances from the inflow of rivers to the lake. The hydraulic heads in the piezometers as well as vertical profiles of Mg⁺², Na/Cl, and Br/Cl were used to investigate both hydraulic and geochemical interactions between surface-water and pore-water in the lake. Depletion of lake surface water and pore water with respect to B, Br, Li⁺, K⁺, Mg²⁺ and the absence of Mg-K chlorides and sulphates in the lake bed sediments is probably due to leakage of highly evaporated residual brine from the lake. Hydraulic gradients in the multilevel piezometric nests indicate that a general downward flow from surface-water to pore-water occurs across sediment–water interface. Vertical profiles of Br/Cl, Mg²⁺, and Na/Cl showed that the maximum flow rate was more than 1 m/yr close to the mouth of the inflowing rivers. The downward vertical flow was limited in the area far from the inflowing rivers due to the presence of an impermeable confining halite layer which interrupts the hydraulic connection between shallow pore water (less than 50 cm deep) and deeper zones. The hydraulic and geochemical interactions between surface-water and pore-water across sediment–water interface in the Maharlu Lake are of interest to find out the fate of pollutants and their distribution in the lake.     

A SEM-based method to determine the mineralogical composition and the particle size distribution of suspended sediment

A robust method for characterizing the mineralogy of suspended sediment in continental rivers is introduced. It encompasses 3 steps: the filtration of a few milliliters of water, measurements of X-ray energy dispersive spectra using Scanning Electron Microscopy (SEM), and robust machine learning tools of classification. The method is applied to suspended particles collected from various Amazonian rivers. A total of more than 204,000 particles were analyzed by SEM-EDXS (Energy Dispersive X-ray Spectroscopy), i.e. about 15,700 particles per sampling station, which lead to the identification of 15 distinct groups of mineralogical phases. The size distribution of particles collected on the filters was derived from the SEM micrographs taken in the backscattered electron imaging mode and analyzed with ImageJ freeware. The determination of the main mineralogical groups composing the bulk sediment associated with physical parameters such as particle size distribution or aspect ratio allows a precise characterization of the load of the terrigenous particles in rivers or lakes. In the case of the Amazonian rivers investigated, the results show that the identified mineralogies are consistent with previous studies as well as between the different samples collected. The method enabled the evolution of grain size distribution from fine to coarse material to be described in the water column. Implications about hydrodynamic sorting of mineral particles in the water column are also briefly discussed. The proposed method appears well suited for intensive routine monitoring of suspended sediment in river systems.     

Sediment export from French rivers to the sea

Knowledge of sediment exports from continental areas is essential for estimating denudation rates and biogeochemical cycles. However, the estimation of current sediment fluxes to the sea is often limited by the availability and quality of sediment discharge data. This study aims to quantify the relative contributions of French rivers to the sediment discharge to the ocean. Sediment fluxes were assessed using the French river quality database, which is characterized by a low temporal resolution but long‐term measurement periods. An improved rating curve approach (IRCA) using daily discharge data, which allows the estimation of mean annual sediment loads from infrequent sediment concentration data, was used to calculate sediment fluxes. The resulting mean annual sediment loads show that French rivers export c. 16.21 Mt yr^‐1 of sediments to the sea. Among the 88 defined French rivers flowing to the sea, the four largest basins (Loire, Rhone, Garonne and Seine) export 13.2 Mt yr^‐1, which corresponds to 81.3% of total exports. No relationship was found between the mass of exported sediment and the size of the drainage basins. This is due to the variety of river basin typologies among these rivers, including lowland rivers in temperate climates, such as the Seine on the one hand and rivers draining mountainous areas in Alpine/Mediterranean areas on the other hand, such as the Rhone. The latter contributes 60% to the total sediment export for France while its drainage area is only 19% of the total area considered. Differences between the river basins considered are also shown by temporal indicators describing the duration of the exports, which may be linked with sediment production processes over drained areas. Copyright © 2012 John Wiley & Sons, Ltd.     

东太湖表层沉积物的磷饱和度初步研究

对东太湖一个横断面上８个样点、１个网围养鱼区样点,１个鱼塘样点的表层１０ｃｍ沉积物含磷量进行了分层采样分析,并以表层沉积物和湖水组成系统,通过磷添加研究了沉积物的磷饱和度。     

Fate of DDT-related compounds in Bohai Bay and its adjacent Haihe Basin, North China

Concentrations of ten DDTs (2,2-bis-(chlorophenyl)-1,1,1-trichloroethane) of which p,p'-DDA (2,2-bis(chlorophenyl)acetic acid), p,p'-DDM (bis(chlorophenyl)methane) and p,p'-DBP (dichlorobenzophenone) are often neglected, were measured in 25 water and 25 sedimentary samples from Bohai Bay and its adjacent Haihe Basin. The ratio of o,p'-DDX/p,p'-DDX in the upper reaches of Yongdingxin River ranged from 0.71 to 2.44, suggesting that the potential source of pollution would be the manufacturing or use of dicofol near this river. While DDA accounted for 52-93% of the SigmaDDT concentration in water, DDA was only detected in three sedimentary samples. And DDM was found to be an important degradation product of DDT in water following DDA. It should be noted that DBP (0.60-3.30 ng/g) is a major metabolite comparable with DDE (2,2-bis(chlorophenyl)-1,1-dichloroethylene, nondetectable-1.80 ng/g) and DDD (2,2-bis-(chlorophenyl)-1,1-dichloroethane, nondetectable-2.86 ng/g) in sediment in Bohai Bay. Finally, the SigmaDDT concentration in sedimentary sample from Bohai Bay was found to be dependent on the TOC (total organic carbon) value.     

Occurrence of perfluorinated compounds in water, sediment and mussels from the Cantabrian Sea (North Spain)

Perfluorinated compounds (PFCs) have emerged as significant global environmental pollutants with persistent, bioaccumulative and toxic properties. The aim of this study was to determine the occurrence of PFCs in water (wastewater, submarine emissaries and port-waters), sediment and transplanted mussels in estuarine areas of high urban and industrial impact from Northern Spain. Five PFCs of industrial use were studied: perfluorooctanesulfonate, perfluorohexanesulfonate, perfluorobutanesulfonate, perfluorooctanoate acid and perfluorononanoate acid. After selective extraction, samples were analyzed by Ultra Performance Liquid Chromatography coupled to tandem mass spectrometry. ΣPFCs ranged from 0.06 to 10.9 ng/L in water, with higher levels in wastewater treatment plants effluents and port waters than in submarine emissaries. Little accumulation was observed in sediments and mussels with ΣPFCs ranging from 0.01-0.13 ng/g dw and 0.01-0.06 ng/g ww, respectively. Most ubiquitous compounds were PFOS and PFOA. Mass fluxes of PFCs to the Cantabrian Sea are estimated and the impact to the coastal ecosystem is discussed.     

Suspended sediment monitoring in alluvial gullies: A laboratory and field evaluation of available measurement techniques

Gully erosion is a significant source of fine suspended sediment (<63 μm) and associated nutrient pollution to freshwater and marine waterways. Researchers, government agencies, and monitoring groups are currently using monitoring methods designed for streams and rivers (e.g., autosamplers, rising stage samplers, and turbidity loggers) to evaluate suspended sediment in gullies. This is potentially problematic because gullies have several hydrological features and monitoring operational challenges that differ to those of continually flowing streams and rivers (e.g., short and intense flows, high suspended sediment concentrations, and rapid scouring and aggradation). Here we present a laboratory and field-based assessment of the performance of common suspended sediment monitoring techniques applied to gullies. We also evaluate a recently-described method; the pumped active suspended sediment (PASS) sampler, which has been modified for monitoring suspended sediment in gully systems. Discrete autosampling provided data at high temporal resolution, however, it had poor collection efficiency (25 ± 10%) of coarser sediment particles (i.e., sand). Rising stage sampling, while robust and cost-effective, suffered from large amounts of condensation under field conditions (25–35% of sampler volume), due to harsh climatic conditions creating large diurnal temperature differences at the field site, thereby diluting sample concentrations and introducing additional measurement uncertainty. The turbidity logger exhibited a highly variable response when calibrated at each site with physically collected suspended sediment samples (R² = 0.17–0.83), highlighting that this approach should be used with caution. The modified PASS sampler proved to be a reliable and representative measurement method for gully sediment water quality, however, the time-integrated nature of the method limits its temporal resolution compared to the other monitoring methods. We recommend monitoring suspended sediment in alluvial gully systems using a combination of complementary techniques (e.g., PASS and RS samplers) to account for the limitations associated with individual methods.     

长江中下游湖泊群落水平下沉水植物碳、氮、磷化学计量特征及其影响因素

以长江中下游14个湖泊沉水植物为研究对象,分析群落水平下沉水植物碳(C)、氮(N)、磷(P)的化学计量特征及其影响因素.结果显示,沉水植物群落C含量平均为386.93±25.80 mg/g,范围为315.98~441.97 mg/g,N和P含量的平均值分别为26.10±4.84和2.64±0.99 mg/g,范围分别为13.75~40.89和1.01~5.92 mg/g.与物种水平研究相比,群落水平下沉水植物C、N、P化学计量特征变异系数较小,内稳定性更强.群落C含量与P含量具有显著相关性,而与N含量不相关,这说明C元素与N和P之间的耦合关系并不一致;N∶P比与P含量之间具有极显著的负相关关系,但与N含量不相关,说明沉水植物群落P含量的变异对N∶P比起主导作用.冗余分析表明,环境因子解释了沉水植物群落化学计量特征总变异的30.2%,在P0.01水平下对沉水植物群落化学计量特征具有显著影响的环境因子为底泥总磷、底泥N∶P比、水深和消光系数.变差分解结果表明,底泥和上覆水分别独自解释了化学计量特征总变异的5.21%和10.19%,其交互作用解释了总变异的5.25%.通过该研究结果推测,在恢复湖泊水生植被的实践过程中,相对于底泥,对上覆水光照条件进行控制可能更加迫切.