Heavy metal release by peat erosion in the Peak District,southern Pennines,UK     

J. J. Rothwell  S. G. Robinson  M. G. Evans  J. Yang  T. E. H. Allott 《水文研究》2005,19(15):2973-2989

Upper North Grain (UNG) is a heavily eroding blanket peat catchment in the Peak District, southern Pennines, UK. Concentrations of lead in the near‐surface peat layer at UNG are in excess of 1000 mg kg⁻¹. For peatland environments, these lead concentrations are some of the highest globally. High concentrations of industrially derived, atmospherically transported magnetic spherules are also stored in the near‐surface peat layer. Samples of suspended sediment taken during a storm event that occurred on 1 November 2002 at UNG, and of the potential catchment sources for suspended sediments, were analysed for lead content and the environmental magnetic properties of anhysteretic remanent magnetization (ARM) and saturation isothermal remanent magnetization (SIRM). At the beginning of the storm event, there is a peak in both suspended sediment and associated lead concentration. SIRM/ARM values for suspended sediment samples throughout the storm reveal that the initial ‘lead flush’ is associated with a specific sediment source, namely that of organic sediment eroded from the upper peat layer. Using the magnetic ‘fingerprinting’ approach to discrimination of sediment sources, this study reveals that erosion of the upper peat layer at UNG is releasing high concentrations of industrially derived lead (and, by inference, other toxic heavy metals associated with industrial particulates) into the fluvial systems of the southern Pennines. Climate‐change scenarios for the UK, involving higher summer temperatures and stormier winters, may result in an increased flux both of sediment‐associated and dissolved heavy metals from eroding peatland catchments in the southern Pennines, adversely affecting the quality of sediment and water entering reservoirs of the region. Copyright © 2005 John Wiley & Sons, Ltd.  相似文献   

Preliminary comparison of trace metals in coastal aerosols between Qingdao and Liverpool     

刘昌岭  张经 《中国海洋湖沼学报》2008,26(2):203-214

Aerosol samples were collected at two coastal suburban stations, Qingdao （China） in 1995-1996 and Liverpool （U.K.） in 1995, respectively. The samples were analyzed to determine the concentrations of trace metals （Cr, Zn, Cu, Co, Ni, Pb, V, and Cd） as well as A1, Fe and Mn. Data were examined to understand the difference of trace metals in aerosols between coastal zones downwind the developing area （near the Yellow Sea） and developed region （near the Irish Sea）. The results show that most elements at Qingdao have levels 4-5 times higher than those at Liverpool, particularly for the crust-dominated elements （e.g. Al, Fe and Mn）. Moreover, the aerosol composition at Qingdao is higher in spring than in summer, underlying the influence of westerlies and local emissions in combination, whereas seasonal change of aerosol composition is not significant at Liverpool. The enrichment factors for the crustal source elements （EFcrust） at Liverpool are much higher than those at Qingdao. The contributions from the pollutant source （Rp） for some trace metals like Cu, Pb, Zn and Cd are 〉90% at Qingdao and Liverpool, suggesting overwhelming anthropogenic contributions to these metals. The contributions from crustal source （Re） for trace metals tend to increase with higher aerosol levels and Al concentration at Qingdao, indicating a good correlation between the crust-dominated component and the air mass. At Liverpool, the Rc values for trace metals are positively correlated with Al concentrations instead of with aerosol mass, suggesting that Al in aerosols represents the crustal component even though the aerosols come from different sources.  相似文献   

Heavy metals,polycyclic aromatic hydrocarbons and organochlorine pesticides in the surface sediments of mangrove swamps from coastal sites along the Leizhou Peninsula, South China     

TANG Yijie  FANG Zhanqiang  YU Shixiao 《海洋学报(英文版)》2008,27(1):42-53

Contents of heavy metals, polycyclic aromatic hydrocarbons （PA Hs）, dichlorodiphenyltrichloroethanes （DDTs） and hexachlorcy- clohexanes （HCHs） in surface sediments from mangrove areas of the Leizhou Peninsula were analyzed in July and November 2005. Risk assessment criteria applied by Long E R et al. （1995） and Long E D et al. （1995） （effects range low, ERL; effects range mean, ERM） of chemicals in sediments from the gulf or estuary were used to assess the potential ecological risks of heavy metals, PAHs, DDTs and HCHs to aquatic organisms in the studied area. The results indicated that the average contents of zinc, nickel, chromium, lead, copper, arsenic and mercury were （61.97 ± 55.87）, （59.99 ± 39.01 ）, （47.93 ± 28.37）, （26.64± 13.00） , （23.45 ± 41.96）, （9.32 ± 3.62）, （0.14 ± 0.18） mg/kg in dry weight in the sediment samples col- lected from five studied sites in the Leizhou Peninsula, respectively. Cadmium was not calculated due to its content being below the detection limit （ 〈 0.3 mg,/kg）. The average levels of Cr, Cu, Ni, Pb, Zn and Hg exceed their background values. The average contents of Ni were higher than ERM. The contents of PAHs in the sediments from the five studied sites were （79.78 ± 43.70） ng/g in dry weight, far lower than ERL（4 022 ng/g）. The contents of DDE, DDD and DDTs in the sediments from five studied sites were （2.60 ± 4.68）, （ 17.52 ± 27.25 ）, （27.78 ± 46.64） ng/g in dry weight respectively, clearly higher than ERL, and the average contents of DDT were （7.66 ± 15.93） ng/g in dry weight, much higher than ERM. HCHs could be detected in the sediments only from Gaoqiao sampling site, with the average contents （0.07 ± 0.08） ng/g in dry weight.  相似文献   

Accumulation of petroleum hydrocarbons and heavy metals in clams （Ruditapes philippinarum） in Jiaozhou Bay, China   总被引：2，自引：0，他引：2  

马海青  宋茜  王旭晨 《中国海洋湖沼学报》2009,27(4):887-897

Accumulation and distributions of aliphatic and polyaromatic hydrocarbons (PAHs) and heavy metals were measured in tissues of the clam Ruditapes philippinarum collected from 5 sites in Jiaozhou Bay, Qingdao, China. The concentrations of total aliphatic hydrocarbon and PAHs ranged from 570 to 2 574 ng/gdw (gram dry weight) and from 276 to 939 ng/gdw, in the most and least polluted sites, respectively. The bio-accumulation of hydrocarbons and PAHs in the clams appeared to be selective. Aliphatic hydrocarbons were predominantly represented by short chain (<nC₂₃) n-alkanes, suggesting that petroleum hydrocarbons were likely the major contamination source. The selective uptake of 3 and 4 ring PAHs, such as naphthalene, fluorene, phenanthrene, fluoranthene and pyrene, by the clams was probably related to the physiological and bio-kinetic processes that were energetically favorable for uptake of compounds with fewer rings. Accumulation of the metals Cd, Cu, Zn, Pb, Cr, Hg, and As in the clam tissues also showed high variability, ranging from 0.043 to 87 μg/gdw. Among the 7 detected metals, Zn, Cd, Cu, and As had a particularly high potential of accumulation in R. philippinarum. In general, a positive correlation was found between the tissue concentrations and sediment concentrations of hydrocarbons and of some metals. Our study suggests that moderate contamination with polyaromatic hydrocarbons, and low to moderate contamination with metals, currently exists for clam R. philippinarum in Jiaozhou Bay, in comparison with other regional studies. A long-term monitoring program is certainly needed for assessment of the potential ecological influence and toxicity of these contaminants of R. philippinarum in Jiaozhou Bay.  相似文献   

Heavy metal pollution of coastal river sediments, north-eastern New South Wales, Australia: lead isotope and chemical evidence     

B. G. Lottermoser 《Environmental Geology》1998,36(1-2):118-126

 Heavy metal and metalloid concentrations within stream-estuary sediments (<180-μm size fraction) in north-eastern New South Wales largely represent natural background values. However, element concentrations (Ag, As, Cd, Cr, Cu, Hg, Ni, Pb, Sb, Zn) of Hunter River sediments within the heavily industrialized and urbanized Newcastle region exceed upstream background values by up to one order of magnitude. High element concentrations have been found within sediments of the Newcastle Harbour and Throsby Creek which drains into urbanized and light industry areas. Observed Pb enrichments and low ²⁰⁸Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁶Pb/²⁰⁴Pb ratios are likely caused by atmospheric deposition of Pb additives from petrol and subsequent Pb transport by road run-off waters into the local drainage system. Sediments of the Richmond River and lower Manning, Macleay, Clarence, Brunswick and Tweed River generally display no evidence for anthropogenic heavy metal and metalloid contamination (Ag, As, Cd, Cr, Cu, Hg, Ni, Pb, Sb, Zn). However, the rivers and their tributaries possess localized sedimentary traps with elevated heavy metal concentrations (Cu, Pb, Zn). Lead isotope data indicate that anthropogenic Pb provides a detectable contribution to investigated sediments. Such contributions are evident at sample sites close to sewage outlets and in the vicinity of the Pacific Highway. In addition, As concentrations of Richmond River sediments gradually increase downstream. This geochemical trend may be the result of As mobilization from numerous cattle-dip sites within the region into the drainage system and subsequent accumulation of As in downstream river and estuary sediments. Received: 5 September 1997 · Accepted: 4 November 1997  相似文献   

Detecting environmental change in estuaries: Nutrient and heavy metal distributions in sediment cores in estuaries from the Gulf of Finland,Baltic Sea     

S. Vaalgamaa  D.J. Conley 《Estuarine, Coastal and Shelf Science》2008

Historical sediment nutrient concentrations and heavy metal distributions were studied in four estuaries in the Gulf of Finland, Baltic Sea to examine the response of these estuaries to temporal changes in human activities. Cores were collected using a 1-m Mackereth corer and dated using ²¹⁰Pb and ¹³⁷Cs. The cores were analyzed for total carbon (TC), total nitrogen (TN), total phosphorus (TP), organic phosphorus (OP), inorganic phosphorus (IP), biogenic silica (BSi), loss-on-ignition (LOI), Cu, Zn, Al, Fe, Mn, K, Ca, Mg and Na. Principal component analysis (PCA) was used to summarize the trends in the chemical variables and to compare the trends at the different sites. Applying the 1986 ¹³⁷Cs date as a reference point, ²¹⁰Pb chronologies were constructed for the sites using either the CRS model or a composite model (using both CIC and CRS). Significant increases were observed in sedimentation rates, TP and TN concentrations in all of the cores. Copper showed clear increases from 1850 towards present at all sites. Furthermore, redundancy analysis (RDA) was used to correlate environmental variables (catchment land use, catchment size, estuary surface area, depth and lake percentage) to sediment geochemistry. Based on redundancy analysis (RDA), the percentage of agriculture in the catchment was the most important factor affecting the sediment accumulation rate. Urban land-use types and industry correlate well with sediment Cu and Ca concentrations. Forest areas were related to high sediment BSi concentrations. Catchment land use was the most significant factor affecting sediment geochemical composition and sediment accumulation rates in these coastal embayments. Our results demonstrate that the coastal estuaries of the Gulf of Finland respond to the increased nutrient loading with the increased sedimentation and nutrient accumulation rates.  相似文献   

Dissolved aluminium and the silicon cycle in the Arctic Ocean   总被引：1，自引：0，他引：1  

R. Middag  H.J.W. de Baar  P. Laan  K. Bakker 《Marine Chemistry》2009,115(3-4):176-195

Concentrations of dissolved (0.2 µm filtered) aluminium (Al) have been determined for the first time in the Eurasian part of the Arctic Ocean over the entire water column during expedition ARK XXII/2 aboard R.V. Polarstern (2007). An unprecedented number of 666 samples was analysed for 44 stations along 5 ocean transects. Dissolved Al in surface layer water (SLW) was very low, close to 1 nM, with lowest SLW concentrations towards the Canadian part of the Arctic Ocean and higher values adjacent to and in the shelf seas. The low SLW concentrations indicate no or little influence from aeolian dust input. Dissolved Al showed a nutrient-type increase with depth up to 28 nM, but large differences existed between the different deep Arctic basins. The differences in concentrations of Al between water masses and basins could largely be related to the different origins of the water masses. In the SLW and intermediate water layers, Atlantic and Pacific inflows were of importance. Deep shelf convection appeared to influence the Al distribution in the deep Eurasian Basin. The Al distribution of the deep Makarov Basin provides evidence for Eurasian Basin water inflow into the deep Makarov Basin. A strong correlation between Al and Silicon (Si) was observed in all basins. This correlation and the nutrient-like profile indicate a strong biological influence on the cycling and distribution of Al. The biological influence can be direct by the incorporation of Al in biogenic silica, indirect by preferential scavenging of Al onto biogenic siliceous particles, or by a combination of both processes. From the slope of the overall Al–Si relationship in the intermediate water layer (AIDW; ~ 200–2000 m depth), an Al/Si ratio of 2.2 atoms Al per 1000 atoms Si was derived. This ratio is consistent with the range of previously reported Al/Si uptake ratio in biogenic opal frustules of diatoms. In the deepest waters (>2000 m depth) a steeper slope of the Al–Si relationship of 7.4 to 13 atoms Al per 1000 atoms Si likely results from entrainment of cold shelf water into the deep basins, carrying the signal of dissolution of terrigenous particles with a much higher Al:Si ratio of crustal abundance. Only a small enrichment with such crustal Al and Si component may readily account for the higher Al:Si slope in the deepest waters.  相似文献   

Impacts of maintenance channel dredging in a northern Adriatic coastal lagoon. I: Effects on sediment properties,contamination and toxicity     

Roberta Guerra  Andrea PasterisMassimo Ponti 《Estuarine, Coastal and Shelf Science》2009

Conservation and management of coastal lagoons envisage direct human intervention. To prevent siltation and to preserve the hydrodynamics features of the lagoon system, the inner channels undergo regular maintenance dredging.  相似文献   

因子克里格分析支持的重金属元素空间多尺度变化特征——以北部湾东北部海域为例   总被引：1，自引：0，他引：1  

赵建如  初凤友  金翔龙  吴清松  杨克红  葛倩  金路 《海洋学报(英文版)》2015,34(12):137-146

将因子克里格分析方法应用于海底沉积物重金属元素空间多尺度变化的研究中,分析了北部湾东北部表层沉积物中7种重金属元素,Ni、Cu、Zn、Pb、Cr、As和Cd的空间多尺度结构特征,识别并分离了重金属元素不同尺度的空间变化,并探讨了各个尺度上重金属的物源及控制因素。结果显示,研究区重金属存在块金效应、变程为30km的球状结构(短变程尺度)和变程为140km的球状结构(长变程尺度)等三种尺度的空间结构,并拟合了研究区7种重金属元素的线性协同区域化模型。短变程尺度上,7种重金属元素的空间分布表现为"点状"或"条带状"的局部尺度的空间变化特征;长变程尺度上,7种重金属元素的空间分布反映出"片状"的区域尺度的空间变化特征。局部尺度上,Zn、Cr、Ni、Cu、Pb和Cd等元素主要源于海南岛、雷州半岛、广西大陆等陆地母岩物质,其空间分布特征受到了沉积物粒度的控制作用;而As主要受到海南岛、雷州半岛的人为污染成分的影响。区域尺度上,Zn、Cr、Ni和Cu主要来源于雷州半岛、海南岛的母岩物质,其次为广西大陆;As主要来源于海南岛的母岩物质,其次为雷州半岛、广西大陆。这些重金属元素在北部湾终年逆时针大环流的控制下,进行搬运、迁移并沉积在"汇聚中心",形成了研究区重金属元素区域尺度上NWW-NNW向的分布格局;而As不同于其他元素的亲陆的NNW向分布特征,主要源于其不同的地球化学行为。  相似文献   

湛江港海域海水和表层沉积物重金属分布特征及其污染评价   总被引：2，自引：0，他引：2  

刘芳文  颜文  苗莉  徐维海 《海洋技术学报》2015,34(2):74-82

根据2013年01月(冬季)和2013年06月(夏季)的调查数据对湛江港海域海水和表层沉积物中的重金属(铜、锌、铅、镉、砷和汞)进行了研究,调查结果显示调查海域海水和表层沉积物中重金属含量呈现岸边海域高于深海海域,东海岛北面海域高于东面海域;对比冬季和夏季的调查结果,调查海域海水中重金属平均含量夏季高于冬季。用单项污染指数对海水中的重金属进行了评价,结果表明,冬、夏两季海水中的Pb污染较明显,Cu和Zn轻度污染,其余元素(Cd,As和Hg)均未超过相应的国家海水水质标准限值,夏季重金属污染指数高于冬季,可能与陆源重金属污染物入海的影响有关;表层沉积物中重金属均低于相应的标准限值,沉积物环境质量状况良好。采用瑞典科学家H覿kanson的潜在生态危害指数法进行评价,沉积物中重金属的潜在生态危害较轻,生态危害程度HgAsCdPbCuZn。  相似文献