Dissolved trace elements and heavy metals from the shallow lakes in the middle and lower reaches of the Yangtze River region,China

Dissolved trace elements and heavy metals of waters and sediments in the ten shallow lakes in the middle and lower reaches of the Yangtze River region were determined to identify their composition and spatial distribution, and to assess the extent of their environmentally detrimental effects by comparison with water and sediment quality guidelines. Results indicated that As and Pb were the main pollutants in lake waters and Mn and Hg the potential ones, while As, Cu and Pb were the main pollutants in lake sediments. Their spatial distribution indicated that Daye Lake was seriously polluted by metals, which was corroborated by cluster analysis. Higher concentrations of trace elements have been found in lakes downstream of the Yangtze River delta, and higher concentrations of metals have been recorded in sediments of upstream lakes, suggesting that metals in water were more sensitive to anthropogenic activities and that metals in sediment were mainly controlled by minerals. Correlation analyses demonstrated that there were stronger associations among metals in lake sediments than those in lake waters, and their good relationships suggested the common sources. Further research on the subject will help develop water quality management with the aim of restoring shallow lakes in the Yangtze River.     

Spatial and temporal variability of trace element concentrations in an urban subtropical watershed,Honolulu, Hawaii

Trace metal concentrations in soils and in stream and estuarine sediments from a subtropical urban watershed in Hawaii are presented. The results are placed in the context of historical studies of environmental quality (water, soils, and sediment) in Hawaii to elucidate sources of trace elements and the processes responsible for their distribution. This work builds on earlier studies on sediments of Ala Wai Canal of urban Honolulu by examining spatial and temporal variations in the trace elements throughout the watershed. Natural processes and anthropogenic activity in urban Honolulu contribute to spatial and temporal variations of trace element concentrations throughout the watershed. Enrichment of trace elements in watershed soils result, in some cases, from contributions attributed to the weathering of volcanic rocks, as well as to a more variable anthropogenic input that reflects changes in land use in Honolulu. Varying concentrations of As, Cd, Cu, Pb and Zn in sediments reflect about 60 a of anthropogenic activity in Honolulu. Land use has a strong impact on the spatial distribution and abundance of selected trace elements in soils and stream sediments. As noted in continental US settings, the phasing out of Pb-alkyl fuel additives has decreased Pb inputs to recently deposited estuarine sediments. Yet, a substantial historical anthropogenic Pb inventory remains in soils of the watershed and erosion of surface soils continues to contribute to its enrichment in estuarine sediments. Concentrations of other elements (e.g., Cu, Zn, Cd), however, have not decreased with time, suggesting continued active inputs. Concentrations of Ba, Co, Cr, Ni, V and U, although elevated in some cases, typically reflect greater proportions attributed to natural sources rather than anthropogenic input.     

Sediment type distribution in reservoirs: sediment source versus morphometry

 Bottom sediments were collected from seven Texas reservoirs to assess the spatial distribution of sediment types in reservoirs. The sediment samples were analyzed for water content, organic content, and grain-size distributions. The reservoirs are characterized by distinct water content patterns (referred to in this paper as Types I, II, and III) that reflect the lithologic units comprising their drainage area. The water content, organic content, and percent mud decreases from Type I (shale, marl) through Type II (limestone-marl-sandstone) to Type III (granite-gneiss-schist-sandstone) reservoirs. Reported elemental concentrations in the reservoir sediments are consistent with concentrations in the dominant rocks within their drainage area. While water depth accounts for part of the spatial distribution, sediment source explains the overall distribution of sediment types. Coarse-grained source rocks, multiple source rocks, and multiple tributaries which input sediment at different points contribute to an inconsistent sediment type distribution. Depending on the sediment source, sand and gravel-size sediments are present in the deeper regions of some reservoirs. This disrupts the classical morphometry (water depth, slope) controlled sediment distribution pattern (coarser sediments in shallower regions and finer sediments in deeper regions) of natural lakes. Thus, the location of tributaries and the type of sediments they carry are the dominant factors that control the sediment type distribution in reservoirs. Received: 16 June 1998 · Accepted: 24 August 1998     

Overbank sediments from central Mexico: an evaluation of their use in regional geochemical mapping and in studies of contamination from modern and historical mining

Overbank sediment sequences in central Mexico display vertical changes in chemistry which can be related to both anthropogenic contamination and natural geological sources and processes. They also show significant lateral chemical variation, at both local and regional levels, which makes the design of a sampling strategy for regional geochemical mapping or contamination studies difficult. This variation is particularly pronounced in drainage basins which have been contaminated by mining activity and limits the use of overbank sediment as a systematic regional geochemical mapping medium. To be used with confidence, overbank sediments require detailed studies of fluvial geomorphology and history, accompanied by accurate age dating. Active drainage sediments are a more viable alternative in areas of historical mining activity, but must be examined carefully in the light of the regional background where levels of contamination are low or the contaminants are buried within the river floodplain.     

Trace metal concentrations in lake and overbank sediments in southern Norway

 As, Be, Cd, Co, Cr, Cu, Hg, Ni, Pb, V, Se and Zn concentrations were determined and compared in lake and overbank sediments from 33 catchments without local pollution sources in southern Norway. There were no significant differences in concentrations of Be, Co, Cr, Cu, Ni, and V in overbank and pre-industrial lake sediments. In areas with shallow overburden, and significant influence from long-range atmospheric pollution, concentrations of As, Cd, Hg, Pb, Se, and Zn in overbank sediments were probably modified by vertical percolating water. In such areas, we suggest using lake sediments as a better sampling medium for mapping pre-industrial concentrations. Pre-industrial lake sediments yield natural concentrations of Hg and Se, which consist of both geogenic and natural atmospheric deposition. Important covariables like organic carbon content, Fe oxides, and fine mineral fraction were generally higher in pre-industrial lake sediments as compared to overbank sediments. By adjusting for such differences overbank sediments could be used as an alternative in mapping background concentrations of trace metals in regions with few lakes. Received: 19 February 1999 · Accepted: 17 April 1999     

Elemental distribution of coastal sea and stream sediments in the island-arc region of Japan and mass transfer processes from terrestrial to marine environments

A total of 49 elements have been identified in 338 coastal sea sediment samples collected from an area situated off the Ise-Tokai region of Japan for a nationwide marine geochemical mapping project. The spatial distribution patterns of the elemental concentrations in coastal seas along with the existing geochemical maps in terrestrial areas were used to define the natural geochemical background variation, mass transport, and contamination processes. The elemental concentrations of coastal sea sediments are determined primarily by particle size and regional differences. Most elemental concentrations increase with a decrease in particle size. Some elements such as Ca, Mn, and Yb are found to exist in large quantities in coarse particles containing calcareous shells, Fe–Mn oxides, and felsic volcanic sediments. Regional differences reflect the mass transfer process from terrestrial areas to coastal seas and the influence of the local marine geology. An analysis of variance (ANOVA) reveals that for many elements, the particle size effect is predominant over regional difference. The mean chemical compositions of coastal sea sediments are similar to those of stream sediments in adjacent terrestrial areas and in the upper crust of Japan. This observation supports the fact that coastal sea sediments have certainly originated from terrestrial materials. However, the spatial distributions of elemental concentrations are not always continuous between the land and coastal seas. The scale of mass movement observed in marine geochemical maps occurs at a distance of 20 km from the river mouth. A detailed examination of the spatial distribution patterns of K (K₂O) and Cr concentrations suggests that terrestrial materials supplied through rivers are deposited near the shore initially, and then gravity-driven processes shift the sediments deeper into the basin. Contamination with heavy metals such as Zn, Cd and Pb was observed in coastal bays surrounded by urban and industrial areas. It is noteworthy that the areas with the highest concentration of these elements usually do not occur near the shore (not near the contamination source) but at the center of the bay. Unexpected low concentrations of Zn, Cd and Pb near shore may either be due to a decreased anthropogenic load in the most recent sediments or to dilution by unpolluted flood sediments.     

Sources,Distribution and Behavior of Major and Trace Elements in a Complex Karst Lake System

Sources and distribution of major and trace elements were investigated in the Plitvice Lakes, a pristine cascade hydrological system of sixteen karst lakes situated in a sparsely populated area of the central Croatia. Water and surface sediment samples from 17 locations, including springs, tributaries and lakes, were analyzed for the content of 22 elements by high-resolution inductively coupled mass spectrometry. Principal component analysis of the collected data set showed that different springs and tributaries displayed distinct multielemental compositions, reflecting primarily the differences in their corresponding geological backgrounds. It was shown that the springs situated in the Upper and Middle Jurassic dolomite bedrock represented the main source of several trace elements, including some toxic metals (Cd, Zn, Ni and Tl), to the Plitvice Lakes system. The concentrations of most of the trace elements (Mn, Fe, Al, Cd, Zn, Cu, Ni, Pb, Co, Cr and Tl) showed decreasing spatial trends in the downstream direction, from sources to the lakes. Such a distribution was interpreted to be a consequence of an efficient removal of the dissolved elements in the lentic parts of the system, mainly by co-precipitation with authigenic calcite and Mn oxides. Nevertheless, most of the elements in the lake sediments were highly correlated with Al, which indicated their prevalent association with terrigenic material. It was shown that the multicascade system of the Plitvice Lakes had an enhanced autopurification efficiency regarding the elimination of most of the trace metals from the aqueous phase.     

The use of overbank sediment for geochemical mapping and contamination assessment: results from selected English and Welsh floodplains

Overbank sediment profiles from floodplains in England and Wales contain a record of both natural geochemical patterns and those showing the influence of man's activities. It has been suggested that this characteristic can be used to allow maps to be compiled which show human impact on the fluvial geochemical environment. Studies reviewed in this paper, however, show that a single overbank profile very rarely spans the period from before anthropogenic disturbance through to the Industrial Revolution and later. Significant lateral variations in metal concentrations occur also over a relatively small area in overbank sediments of the same general age. These, and the nature of vertical changes in chemistry, make the choice of sample sites, and sampling interval within a profile, difficult. Even sediments which appear uncontaminated may record anthropogenic influences from activities such as deforestation and agriculture. A means of dating the sediment and an appreciation of river erosion and sedimentation histories are shown to be essential in order to ensure that maps intended to depict natural geochemical variations are based on material deposited before disturbance of the catchment by human activity. These considerations and associated costs may render overbank sediment non-viable as a regional geochemical mapping medium.     

Zn, Pb, Cu and As distribution patterns in overbank and medium-order stream sediment samples: their use in exploration and environmental geochemistry

Overbank and medium-order stream sediment samples were collected in Belgium and Luxembourg from 66 sampling locations (area of about 33,000 km²) and analysed for major and trace elements among which Zn, Pb, Cu and As. At each sampling location large bulk samples were taken, namely in the lower (normally at ≥1.5 m depth, over an interval of about 20–40 cm) and upper (normally upper 5–25 cm) parts of the overbank profiles and from the stream sediments. Furthermore, at a number of these sites, a detailed geochemical analysis of vertical overbank sediment profiles (sampling intervals of 10–20 cm) was subsequently carried out to unravel element variations through time and to help in the overall evaluation. For most sampled sections evidences such as ¹⁴C-dating and the absence of anthropogenic particles point towards a pre-industrial and often pristine origin of the lower overbank sediment samples. From the latter bulk samples, mean background concentrations were deduced. They reveal the existence of significant differences between the northern and southern part of Belgium (incl. Luxembourg) which relate to the difference in geological substrate. In the north dominantly non-lithified Quaternary and Tertiary sands, marls and clays occur while in the south Palaeozoic sandstones, shales and carbonate rocks outcrop. Consequently separate mean background values were calculated for the two areas. In the southern study area, some anomalous metal concentrations have been recorded in pre-industrial sediments. They are derived from mineralised Palaeozoic rocks, a feature which could be of interest for base metal exploration. In the upper overbank and stream sediments, in general, higher heavy metal and As contents were recorded with highest values in areas with metal mining, metal melting and cokes treatment industries. By comparing the trace element concentrations of the upper overbank or stream sediment samples with the concentrations detected in the lower overbank samples at each of the sampling locations, and by evaluating the vertical distribution patterns where available, the degree of pollution of the alluvial plain and the present-day stream sediments can be assessed. From this exercise, it is clear that highest pollution occurs in the northern part of Belgium, which relates to its high population density and industrial development.     

Distribution of trace elements in the coastal sea sediments of Maslinica Bay, Croatia

Spatial distributions of trace elements in the coastal sea sediments and water of Maslinica Bay (Southern Adriatic), Croatia and possible changes in marine flora and foraminifera communities due to pollution were investigated. Macro, micro and trace elements’ distributions in five granulometric fractions were determined for each sediment sample. Bulk sediment samples were also subjected to leaching tests. Elemental concentrations in sediments, sediment extracts and seawater were measured by source excited energy dispersive X-ray fluorescence (EDXRF). Concentrations of the elements Cr, Cu, Zn, and Pb in bulk sediment samples taken in the Maslinica Bay were from 2.1 to over six times enriched when compared with the background level determined for coarse grained carbonate sediments. A low degree of trace elements leaching determined for bulk sediments pointed to strong bonding of trace elements to sediment mineral phases. The analyses of marine flora pointed to higher eutrophication, which disturbs the balance between communities and natural habitats.     

湘江下游河床沉积物元素地球化学背景值估算

本研究对湘江下游河床沉积物进行了元素地球化学分析,在认识沉积物元素地球化学特征、甄别人为源与自然源重金属的基础上,估算了沉积物的元素地球化学背景值。结果表明:SiO2、TiO2、Al2O3、Fe2O3、K2O等主量元素及V、Co、Cr、Ba、Sc、U、Sr、Ga、Ge、Rb、Nb、Y、REE等微量元素在沉积物中含量变化相对稳定(Cv<0.2),分布相对均匀,且富集不明显(EF<2.0,Sr明显亏损)。而MnO、MgO、CaO、Na2O、P2O5等主量元素,及Cd、Mn、Cu、Pb、Zn等重金属在沉积物中含量变化大(Cv>0.25),分布极不均匀,且沉积物中重金属明显富集(EF>2.0)。主成分及Pearson线性相关性分析显示,沉积物中不明显富集的微量元素主要赋存于难溶硅酸盐矿物相中,为自然源元素。而沉积物中显著富集的重金属主要赋存于铁—锰氧化物等矿物相中,为有人为源叠加的元素。故针对不同来源特征的元素用不同的方法进行了背景值计算,求得沉积物中47个元素的背景值。再利用元素比值等方法对所得背景值进行检验。结果表明,本文得到的湘江沉积物元素背景值合理,可用作流域沉积物重金属污染评价参考。     

Dispersion of tailings in the Knabena—Kvina drainage basin, Norway, 1: Evaluation of overbank sediments as sampling medium for regional geochemical mapping

Molybdenum mining in the Knabena—Kvina drainage basin (1918–1973) left more than eight million tons of tailings in two small lakes in the headwater area of the Knabena river. The piles, that reach above the water surface, were freely eroded until a dam was built to reduce the dispersion in 1976. Sampling of tailings and fluvial sediments took place almost 20 years later. Sampling media were natural sediment sources, 1-cm-thick slices of overbank sediments of various depths, material from the tailings pond, sandbars, stream sediments, fjord sediments, and integrated samples of floodplain surfaces (0–25 cm). In total 734 samples were collected. Chemical analysis (ICP-AES after aqua regia or HNO₃ extraction) showed that overbank sediments at a certain depth represent the pre-industrial trace metal concentrations within the drainage basin. The tailings and recent fluvial sediments were enriched in approximately the same element suite. The highest enrichment factors were obtained for Cu (8–53) and Mo (22–57). Fluvial processes in the tailings pond have probably selectively eroded fine-grained, low-density particles. Thus, coarse chalcopyrite may have been left behind, while molybdate associated with fine-grained particles may have been selectively entrained causing dilution of Cu and enrichment of Mo in the downstream fluvial sediments. In the sandbars, the highest Cu and Mo concentrations were found in fine-grained sediments downstream of a low-gradient reach that act as a bedload trap. On the floodplains, it is seen that the first areas to be inundated in a flood situation (proximal to the river and in depressions) have the highest metal concentrations. For regional geochemical mapping it is suggested that overbank sediment profiles along river reaches with a laterally stable or slowly migrating channel, should be sampled. In such floodplains, pre-industrial overbank sediments are usually preserved at depth. In case of laterally unstable reaches upstream of the sampling point, polluted and unpolluted sediments may be interlayered or mixed. Therefore, samples should be collected from various depths or sedimentary units in such profiles. A similar sampling strategy should probably be adopted to detect vertical migration of elements especially in areas with acid rain and low bedrock buffer capacity. To obtain high contrasts between polluted and unpolluted drainage basins, the overbank sediment profiles should be within the proximal part of the floodplain.     

福建近岸浅海沉积物元素丰度及含量变化特征

通过福建省沿海经济带生态地球化学调查,在福建近岸浅海区域共采集479件沉积物样品,分析测试了52种化学元素以及pH值和有机碳等指标。总结了该区域浅海沉积物化学元素的丰度、含量变化及其区域分布,并分不同沉积物类型统计有害元素的污染起始值。福建近岸浅海沉积物与中国浅海沉积物对比,大部分元素的含量高于中国浅海沉积物,含量变化基本遵循“元素的粒度控制律”,除Si元素相反外,Al、Fe、Cu、Co、Ni等绝大多数元素的含量随沉积物粒度变细（砂→粉砂→泥）而升高,有些元素在泥质沉积物中的含量常高出砂质的数倍;其高值、高背景区的区域分布也总是与细粒沉积物有关,而低值、低背景区则明显地与砂质沉积物的分布相关。     

Major and trace element geochemistry of superficial sediments and suspended particulate matter of shallow saline lakes in Eastern Austria

General geochemical parameters of water, superficial sediments, and suspended particulate matter (SPM) were determined from small shallow saline lakes (soda ponds) as well as from lake Neusiedlersee in eastern Austria. Additionally, instrumental neutron activation analysis (INAA) was used to determine the distribution of major, rare earth and other trace elements in superficial sediments and SPM. Chemical results show remarkable differences in salinity and ionic strength between the investigated ponds. Anthropogenic effects, such as drawdown of ground water level and a loss of lake water due to drainage, are clearly reflected in obtained chemical and geological data. Due to a strong dependence of the complexation and scavenging behavior of the rare earth elements (REE) on ionic strength, a significant difference between REE concentrations in soda ponds with different anthropogenic impact was found. The content and composition of authigenic evaporitic minerals in superficial sediments and SPM clearly differ with a fluctuating water level and salt concentration. Furthermore, we determined the distribution of major and trace elements in superficial sediments of a nearby fluvial system. Our results show a clear correlation between REE superficial sediment concentrations in anthropogenically degraded soda ponds and fluvial system. Therefore, we assume that REE concentrations of sediments and SPM are suitable for the study of geochemical changes of inland saline lakes due to anthropogenic impacts on water balance.     

High spatial resolution sampling of metals in the sediment and water column in Port Jefferson Harbor, New York

Eighteen sediment samples and six water-column samples were collected in a small (6 km²), coastal embayment (Port Jefferson Harbor, New York) to define a high-resolution spatial distribution of metals and to elucidate sources of contaminants to the harbor. Sediment metal (Ag, Cu, Fe, Ni, Pb, V, and Zn) concentrations varied widely, reflecting differences in sediment grain size, with higher metal concentrations located in the fine-grained inner harbor sediments. Calculated enrichment factors for these sediments show that Ag, Pb, Cu, and Zn are elevated relative to both crustal abundances and their respective abundances in sediments in central Long Island Sound. Metal concentrations were 1.2 to 10 fold greater in water from the inner harbor compared to water from Long Island Sound collected outside the mouth of the harbor. Spatial variations in trace metals in surface waters within the bay parallel the spatial variations of trace metals in sediments within the harbor. Elevated water-column metal concentrations appear to be partially derived from a combination of diagenetic remobilization from contaminated sediments (e.g., Ag) and anthropogenic sources (e.g., Cu and Zn) within the southern portions of the harbor. Although the National Status and Trends Program had reported previously that sediment metal concentrations in Port Jefferson Harbor were low, the results of this study show sediment metals have high spatial variability and are enriched in the inner harbor sediments at levels comparable to more urbanized western north shore Long Island harbors.     

Influence of sediment provenance on background values of potentially toxic metals from near-surface sediments of Po coastal plain (Italy)

Systematic variability in metal concentrations is recorded in near-surface (1 m deep) Late Quaternary sediments of Po coastal plain, across the boundary between alluvial deposits of Apenninic provenance and a formerly active, now abandoned, delta lobe of the Po River. In the latter area, high Cr and Ni concentrations, exceeding the national standard limits, are attributed to sediment provenance from ultramafic source rocks of Po catchment basin, and not to anthropogenic impact. Spatial distribution of carbonate-related elements, such as Ca and Sr, displays consistent differences between the two areas, confirming a primary control of provenance domains on sediment composition. Accurate facies characterization of near-surface sediments, coupled with detailed information on sediment dispersal patterns, enable a reliable interpretation of the spatial variability of major elements and trace metals in the study area. Particularly, detailed reconstructions of source area composition and changes in flow directions through historical times allow precise correlation of apparently anomalous geochemical patterns with distinctive depositional events, such as shifts in channel course, crevasse splay formation and beach-ridge evolution. The findings of unusually high, natural (provenance-controlled) heavy metal concentrations in pre-industrial near-surface levels highlight the contribution of a sedimentological approach to a reliable interpretation of geochemical data. This should be taken into account when determining background values versus anthropogenic impact.     

Concentration distribution and assessment of several heavy metals in sediments of west-four Pearl River Estuary

Grain size parameters, trace metals (Co, Cu, Ni, Pb, Cr, Zn, Ba, Zr and Sr) and total organic matter (TOM) of 38 surficial sediments and a sediment core of west-four Pearl River Estuary region were analyzed. The spacial distribution and the transportation procession of the chemical element in surficial sediments were studied mainly. Multivariate statistics are used to analyses the interrelationship of metal elements, TOM and the grain size parameters. The results demonstrated that terrigenous sediment taken by the rivers are main sources of the trace metal elements and TOM, and the lithology of parent material is a dominating factor controlling the trace metal composition in the surficial sediment. In addition, the hydrodynamic condition and landform are the dominating factors controlling the large-scale distribution, while the anthropogenic input in the coastal area alters the regional distribution of heavy metal elements Co, Cu, Ni, Pb, Cr and Zn. The enrichment factor (EF) analysis was used for the differentiation of the metal source between anthropogenic and naturally occurring, and for the assessment of the anthropogenic influence, the deeper layer content of heavy metals were calculated as the background values and Zr was chosen as the reference element for Co, Cu, Ni, Pb, Cr and Zn. The result indicate prevalent enrichment of Co, Cu, Ni, Pb and Cr, and the contamination of Pb is most obvious, further more, the peculiar high EF value sites of Zn and Pb probably suggest point source input.     

Geochemistry of trace elements in surface waters of the Arno River Basin,northern Tuscany,Italy

Trace element geochemistry of the Arno River and its main tributaries was investigated on the basis of two sampling campaigns carried out in November 1996 and June 1997. By analyzing filtered and unfiltered water samples, Fe and Al are found in solution mainly as colloidal particles of size lower than 0.45 μm. In June (lower flow rate), Fe and Al are enriched in the filtered waters from the main river, and this feature was interpreted in terms of higher water temperature promoting the formation of smaller particles, thus reducing their aggregation properties. Iron and Al show perfectly synchronous downstream profiles along the Arno River, correlate quite well each to other, and display abrupt concentration increases near to Florence, where the lithology of the catchment changes from siliciclastic dominated to clay-sand (lacustrine-marine)-dominated. The same behaviour is shown by most of the other trace elements in the river, thus supporting a general lithological control. Trace elements in the final part of the Arno River are influenced by flocculation processes in addition to mixing. Adsorption phenomena on oxy-hydroxides are denoted by good elemental correlations with Fe (and Al). Sporadic anomalous concentration values, possibly related to anthropogenic contributions, may prevent such correlations. Referring to the quality of waters for potable use and fish life, toxic elements are below the acceptable limits of current European regulations, with few exceptions for Hg exceeding guideline values. Multivariate analysis groups trace elements according to geochemical affinities and natural or anthropogenic sources, thus distinguishing contaminated from uncontaminated samples. The results achieved in this work will help regional and national Authorities for compliance with the EU water policy, especially in assessing the water quality at the river basin scale and its vulnerability to human activities.     

Geochemistry of overbank and high-order stream sediments in Belgium and Luxembourg: a way to assess environmental pollution

A geochemical survey of Belgium and Luxembourg was carried out as part of an international research project entitled ‘Regional geochemical mapping of Western Europe towards the year 2000'. The aim of this research was to map regional background geochemical patterns based on pristine or at least pre-industrial overbank samples and to deduce regional information on the degree of environmental pollution of floodplain and present-day river sediments. Over the entire study area (about 33,000 km²), 66 overbank sites have been sampled. Catchment areas range between 60 and 600 km². At each site an overbank profile has been dug out in the immediate vicinity of the river and described in detail. A first composite sample was taken 5–25 cm below the surface. This sample is supposed to represent deposition over the last centuries. Human interferences in this interval are often inferable based on changed sedimentary characteristics and the presence of anthropogenic particles such as charcoal, slags and brick fragments. A second composite sample was taken at depth, usually >1.5 m below the surface over an interval of about 20 cm. In most sites, the profile characteristics allowed to assume pre-industrial or even pristine conditions for this lower overbank sample. In some profiles this was confirmed by ¹⁴C-dating and/or by the absence of anthropogenic particles. Finally, a present-day stream sediment was sampled on the site to infer the actual pollution status. After drying at 80°C, disaggregation and sieving, the <125 μm fractions of the three sediment samples were analysed by XRF for major elements and several trace elements. Lower overbank samples generally show a direct link with the geological substrate and allow to assess natural background concentrations. Results from the mapping exercise as well as from the statistical analyses display a clear contrast between the northern part of Belgium where Cenozoic unconsolidated sandy and silty formations dominate which are especially vulnerable for erosion, and the southern part of Belgium and Luxembourg where Paleozoic and Mesozoic sandstones, carbonates, marls and shales are the prevalent lithologies. Here the shales are the most intensively eroded lithologies. This is especially reflected in the element patterns of Al₂O₃, MgO, K₂O, Ga, Ni, Rb, Sc and V which negatively correlate with SiO₂. Despite the human related pollution, the geological contrast between north and south Belgium is still recognisable in the geochemical pattern of the upper overbank and present-day stream sediment samples for the above-mentioned elements. Furthermore there is a clear increase in heavy metal contents (Zn, Cd, Pb, Cu), As and in certain locations in Ba from the lower to the upper overbank sediment, as well as to the present-day stream sediment. The relative increase in element content allows to assess the degree of pollution and helps to define those drainage areas where more detailed research is needed.     

http://www.sciencedirect.com/science/article/pii/S1674987115000584

The spatial distribution patterns of surficial sediment samples from different sedimentary domains(shallow to deep-sea regions) of the eastern Arabian Sea were studied using sediment proxies viz.environmental magnetism,geochemistry,particle size and clay mineralogy.Higher concentrations of magnetic minerals(high x_(lf)) were recorded in the deep-water sediments when compared with the shallow water sediments.The magnetic mineralogy of one of the shallow water samples is influenced by the presence of bacterial magnetite as evidenced from the x_(ARM)/x_(lf)~(vs).x_(arm_/x_(fd)biplot.However,the other samples are catchment-derived.The high correlation documented for x_(lf).anhysteretic remanent magnetisation(x_(arm)) and isothermal remanent magnetisation(IRM) with Al indicates that the deep-sea surficial sediments are influenced by terrigenous fluxes which have been probably derived from the southern Indian rivers,the Sindhu(the Indus) and the Narmada-Tapti rivers.A lower Mn concentration is recorded in the upper slope sediments from the oxygen minimum zone(OMZ) but a higher Mn/Al ratio is documented in the lower slope and deep-sea sediments.Clay minerals such as illite(24-48.5%),chlorite(14.1-34.9%),smectite(10.6-28.7%) and kaolinite(11.9-27.5%) dominate the sediments of shallow and deep-sea regions and may have been derived from different sources and transported by fluvial and aeolian agents.Organic carbon(OC) data indicate a low concentration in the shallow/shelf region(well oxygenated water conditions) and deeper basins(increased bottom-water oxygen concentration and low sedimentation rate).High OC concentrations were documented in the OMZ(very low bottom-water oxygen concentration with high sedimentation rate).The calcium carbonate concentration of the surface sediments from the continental shelf and slope regions( 1800 m) up to the Chagos-Laccadive Ridge show higher concentrations(average = 58%) when compared to deep basin sediments(average = 44%).Our study demonstrates that particle size as well as magnetic grain size,magnetic minerals and elemental variations are good indicators to distinguish terrigenous from biogenic sediments and to identify sediment provenance.