Regional geochemistry of trace elements in Chesapeake Bay sediments

The concentrations of Cr, Mn, Fe, Co, Ni, Cu, Zn, Cd, and Pb in 177 surface sediment samples from throughout Chesapeake Bay are reported. Analyses were made of both unfractionated samples and the <63 μm fractions. Analytical uncertainty, always less than ±10%, controlled reproducibility in analyses of the <63 μm fractions, but sampling variance controlled reproducibility in the unfractionated samples, especially when coarse-grained sediments were being analyzed. Sediments in the northernmost part of the bay are enriched relative to average continental crust in all elements except Cr. This reflects the composition of dissolved and suspended material being delivered to that region by the Susquehanna River. The enriched sediments appear not to be transported south of Baltimore in significant quantily. Zinc, cadmium, and lead are enriched relative to average crust throughout the bay and in most other estuaries in the eastern United States.     

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.     

Spatial distribution and geochemical baselines of major/trace elements in soils of Medak district,Andhra Pradesh,India

Regional-scale variations in soil geochemistry were investigated with special reference to differences among soil groups and lithology in an area of 9,699 km² in Medak district, Andhra Pradesh, India. The concentrations of 29 elements (major: Si, Al, Fe, Mn, Mg, Ca, Na, K, Ti, P and trace: As, Ba, Cd, Co, Cr, Cu, F, Mo, Ni, Pb, Rb, Se, Sr, Th, U, V, Y, Zn, Zr) in 878 soil samples collected (557-topsoil, 321-subsoil) at a sampling density of 1 site/17 km² from 557 sites representative of all the soil types present in studied area were determined, and their elemental composition are discussed. The baseline levels of these elements in soils are determined over different lithological units for the identification of anomalous values relative to these. For the first time, geochemical maps for Medak district are prepared on 1:50,000 scale and the lithogeochemical database generated provides information on the lateral and vertical distribution of elements in soil. The spatial variations in the distribution of elements reflect underlying geologic characteristics. Box-plots reveal that the concentration of most of the elements in soils were not strongly dependent on the soil group but the soil-geochemistry abruptly changes with the change in the soil parent materials indicating that the distribution of elements is mostly influenced by the bedrock lithology and other natural processes acting on them. For instance, the concentrations of Co, Cu, Fe, Mn, Ti, V and Zn are high in soils developed on basaltic terrain while the soils developed on granitic and gneissic terrain exhibit high elemental concentrations of K, Pb, Rb, Si, Th and Y. Alfisols had relatively high contents of elements while entisols had lower concentrations of most of the elements. The database can be used in the chemical characterisation of different geological units as well as applications in various environmental and agricultural fields. The results indicate that regional geology is an important determinant of soil geochemical baselines for soil pollution assessment and further emphasizes the importance of determining background levels locally. The defined baselines can be used to establish background values for future soil surveys.     

Composition and variation of major and trace elements in Croatian bottled waters

Within the framework of the Pan-European project about the geochemistry of bottled mineral waters in Europe launched in 2007 by the European Geological Surveys (EGS) Geochemistry Expert Group fourteen brands of bottled natural waters from Croatia of both mineral and spring types were evaluated for getting more coherent spatial information about the natural variation of element concentration in bottled waters found at the European market. Results of chemical analysis show that not a single one out of fourteen analyzed bottled waters from Croatia exceeds the Croatian water standards sanctioning thereby their suitability for human consumption. Also, statistical tests performed for 41 analytes (including pH and EC) clearly show that the water chemistry is in a high degree of conformity with regional geology, depending on structural, stratigraphic and, above all, lithological diversity of aquifers. Thus Dinaric and Pannonian parts of Croatia differ largely with regard to their water types: Dinaric region is completely lacking mineral water types while, on the other side, in the Pannonian region even the spring waters show stronger mineralization in comparison with their Dinaric counterparts. Typically, all natural waters from Croatia bear the bicarbonate (HCO₃) signature. However, Ca–Mg cation pair combination is characteristic of spring waters while Na–K dominates in the mineral waters.     

Spatial distribution of major and trace elements in shallow reservoir sediments: an example from Lake Waco, Texas

 Sediment geochemistry of a shallow (6-m average) reservoir (Lake Waco) was evaluated for the spatial distribution of major and trace elements. Sixty bottom and core samples along a 21-km transect within the reservoir, 18 overbank sediment samples, and 8 rock types in the drainage area were collected and analyzed for major (Al, Ca, Fe) and trace elements (As, Ba, Cr, Cu, Hg, Mn, Ni, Pb, Sr, V, Zn). Elemental concentrations in the reservoir sediments closely correspond to concentrations in the regional rocks and represent a mixture of overbank sediment composition of the tributaries. Elemental concentrations were statistically regressed against Al concentrations in order to establish regional baseline levels and thereby distinguish natural from anthropogenic sources. Spatial geochemical trends, considered in terms of element-to-Al ratio versus V-to-Al ratio, relate to the natural and anthropogenic sources contributing to the elemental concentrations. The spatial elemental distribution in the reservoir, which receive sediments from two mineralogically contrasting basins, reflect textural and mineralogical transition within the reservoir and suggest a progressive mixing of sediment from the tributaries. The spatial elemental distribution and sediment texture suggest that the sediment-source, which determines the sediment-type, has a greater influence on the major- and trace-element distributions in shallow reservoir sediments than bathymetry. Received: 25 September 1997 · Accepted: 3 February 1998     

Geographical variations of trace elements in sediments of the major rivers in eastern China

 A total of 26 geographically and hydrologically diverse sediment samples were collected from 12 major rivers in eastern China. The <63-μm fraction of the sediments was analysed for both total concentrations of Cu, Zn, Pb and Cd, and their associations with various geochemical phases. The geographical variations of sediment-bound trace metals can be related to the bedrock types and weathering processes in the corresponding river basins. The rivers in southern China had notably higher concentrations of trace metals in sediments because of abundant non-ferrous mineral deposits and stronger weathering process in the region. A large proportion of trace metals in these sediments was associated with iron and manganese oxides and organic matter. Relative low levels of trace metals were found in river sediments in northern China, and a significant proportion of the metals was bound to organic matter, carbonates, and the residual fraction. The sediments in the Yellow River, originating from special loess, had the lowest concentrations of trace metals. Most of the trace metals were associated with the carbonates and residual phases. Received: 24 March 2000 · Accepted: 11 July 2000     

Geochemical factors controlling accumulation of major and trace elements in Greenland coastal and fjord sediments

 The major (Al, Ti, Ca, Mg, Fe, Mn, Si) and trace element (Cd, Cr, Cu, Hg, Li, Ni, Pb, V, Zn) concentrations in surficial (<20 cm) sediments from fjords and open coastal waters around Greenland have been determined. Regionally, high concentrations of Fe, Ti, Mg, Cr, Cu, Ni, and V occur in some west and east coast sediments, but they appear to be natural in origin, as there is no indication of anthropogenic influence. Chemical partition indicates that most of the heavy metals are structurally bound in various silicate, oxide, and sulfide minerals. These host minerals occur more or less equally in the coarse and fine sediment fractions (material >63 μm and <63 μm) and have accumulated at the same rate as other detrital clastic material. Provenance and glaciomarine deposition are the main factors controlling the abundance and distribution of the major and trace elements. The chemical composition reflects the mineralogical differences in the provenance of glacial marine material deposited by water and ice adjacent to Greenland. The main source of the sediments enriched in Ti, Fe, Mg, Cr, Cu, Ni, and V appears to be material derived from the volcanic rocks of the Mesozoic-Tertiary Provinces of Greenland by glacial erosion. Received: 26 June 1995 · Accepted: 11 August 1995     

Climate implications of major geochemical elements in the Holocene sediments of the North and East China monsoonal regions

Two Holocene sediment cores were retrieved respectively from the enclosed Lake Daihai in the monsoon/arid transition zone of North China and the Taihu Lake coast in the monsoonal area of the Yangtze delta, Eastern China. Distribution of major geochemical elements and their ratios were employed to reveal the characteristics of Holocene climate and associated environmental implications in the two regions. It is suggested that the temporal distribution of major elements serve as a useful indicator to denote the variations of monsoon effective precipitation for the enclosed lake area. High values of resistant elements such as Al₂O₃, SiO₂, TiO₂, (FeO + Fe₂O₃), MnO in the lake sediments correspond to the depressed chemical weathering and weakened mon-soon effective precipitation, while the highs of mobile and easy soluble elements such as MgO, CaO, Na₂O reflect the enhanced chemical weathering and increased monsoon effective precipitation in the lake basin. In comparison, the behaviors of the major elements in sediments of the Taihu Lake coast were largely controlled by the changes both in sea transgression in the different Holocene time periods and the monsoon precipitation. The relatively highs of Al₂O₃, TiO₂, (FeO + Fe₂O₃), in marine-influenced sediments suggest relatively strong coastal hydrodynamics and chemical weathering, and vice versa. Meanwhile, the lows of SiO₂, Na₂O and CaO in the non-marine-influenced sediments also denote relatively strong hydrodynamics and chemical weathering due to enhanced monsoon precipitation, and vice versa. Sedimentary environment should be taken into account when achieving a full understanding of their climate implications.     

Distribution and partitioning of major and trace elements in pyrite-bearing sediments of a Mediterranean coastal lagoon

The formation of iron sulphide minerals exerts significant control on the behaviour of trace elements in sediments. In this study, three short sediment cores, retrieved from the remote Antinioti lagoon (N. Kerkyra Island, NW Greece), are investigated concerning the solid phase composition, distribution, and partitioning of major (Al, Fe) and trace elements (Cd, Cu, Mn, Pb, and Zn). According to ²¹⁰Pb, the sediments sampled correspond to depositions of the last 120 years. The high amounts of organic carbon (4.1–27.5%) result in the formation of Fe sulphides, predominantly pyrite, already at the surface sediment layers. Pyrite morphologies include monocrystals, polyframboids, and complex FeS–FeS₂ aggregates. According to synchrotron-generated micro X-ray fluorescence and X-ray absorption near-edge structure spectra, authigenically formed, Mn-containing, Fe(III) oxyhydroxides (goethite type) co-exist with pyrite in the sediments studied. Microscopic techniques evidence the formation of galena, sphalerite and CuS, whereas sequential extractions show that carbonates are important hosts for Mn, Cd, and Zn. However, significant percentages of non-lattice held elements are bound to Fe/Mn oxyhydroxides that resist reductive dissolution (on average 60% of Pb, 46% of Cd, 43% of Zn and 9% of Cu). The partitioning pattern changes drastically in the deeper part of the core that is influenced by freshwater inputs. In these sediments, the post-depositional pyritization mechanism, illustrated by overgrowths of Fe monosulphides on pre-existing pyrite grains, results in relatively high degree of pyritization that reaches 49% for Cd, 66% for Cu, 32% for Zn and 7% for Pb.     

Distribution of Rare—earth Elements in the Shenzhen Bay and Dapeng Bay Modern Sediments

The aim of this paper is to study the REE geochemistry of the Shenzhen Bay (SZB) and Dapeng Bay(DPB) modern sediments, discuss their REE distribution patterns, reveal the REE geochemical difference between the two bays which share the same material source but are deposited in different sedimentary environments, and expound their dynamic changes.It can be concluded that the SZB and DPB sediments are essentially of continental source.Their REE distribution patterns are quite different from those of Pacific pelagic sediments, but are very similar to those of South Chi-na granites.Because of different sedimentary environments prevailing in the SZB and DPB, some REE fractionation would have taken place in the sediments of the two bays.     

海底沉积物中不同形式烃类气体的地球化学意义

顶空气法和酸解烃法将东沙群岛海域海底浅表层沉积物中不同形式的烃类气体释放出来,通过分析两类气体在沉积物中的含量及其甲烷碳同位素,发现两类气体的成因和来源不同。笔者认为,相对而言,吸附气(包裹气)反映的是一种更为早期的信息,而游离气(溶解气)则更具有“现代性”。笔者进一步认为,两类气体的不同形成过程,对于天然气水合物调查具有不同的意义,其中游离气(溶解气)具有直接的指示意义,而吸附气(包裹气)可能指示成岩时沉积物中的空间信息。     

Spatial variation of probabilistic seismic hazard for Mumbai and surrounding region

Mumbai city, the economical capital of India, is located on the west coast of stable intra-plate continental region of Peninsular India which has an experience of significant historical earthquakes in the past. The city stood as the fourth most populous city in the world. Recent seismo-tectonic studies of this city highlighted the presence of active West coast fault and Chiplun fault beneath the Deccan basalt. In the present study, spatial variability of probabilistic seismic hazard for Mumbai region (latitudes of 18.85–19.35°N and longitudes of 72.80–73.15°E at a grid spacing of 0.05°) which includes Mumbai city, Suburban, part of Thane district and Navi Mumbai, in terms of ground motion parameters; peak horizontal acceleration and spectral acceleration at 1.0-s period for 2 and 10 % probability of exceedance in 50 years are generated. The epistemic uncertainty in hazard estimation is accounted by employing seven different ground motion prediction equations developed for worldwide shallow crustal intra-plate environments. Further, the seismic hazard results are deaggregated for Mumbai (latitude 18.94°N, longitude 72.84°E) to understand the relative contributions of earthquake sources in terms of magnitude and distance. The generated hazard maps are compared with the zoning specified by Indian seismic code (IS1893: Part 1 in Indian standard criteria for earthquake-resistant design of structures, Part 1—General provisions and buildings. Bureau of Indian Standards, New Delhi, India, 2002) for rocky site. Present results show an underestimation of potential seismic hazard in the entire study region by non-probabilistic zoning prescribed by IS1893: Part 1 with significantly higher seismic hazard values in the southern part of Navi Mumbai.     

Impact of historical metalworks on the concentrations of major and trace elements in sediments: a case study in Finland

The concentrations of major and trace elements were determined (aqua regia leach and ICP-AES analyses) in stream, lake and dredged sediments downstream of the historical Antskog iron- and copperworks, S.Finland. The levels of Ag, Cd, Cu, Pb and Zn are highly elevated in all studied sediment types: roughly half of the studied lake-sediment samples contain >5 ppm Ag, >15 ppm Cd, >0.1% Cu, >0.1% Pb and >0.3% Zn. In the dredged sediment material located onshore, the concentrations of Ag, Cu and Pb are comparable to those in the polluted lake-sediment samples, while in stream sediments elevated metal concentrations are found especially in samples characterised by high concentrations of organic material. The source of the elevated metal concentrations is the historical metalworks at Antskog, mainly the copperworks of the 19th century. Compared to the limit values for contaminated soils in Finland, the concentrations of Cu, Pb and Zn are on average elevated by factors >10 in the polluted horizons of lake sediments, >5 in the dredged sediment located onshore and >2 at the most heavily contaminated site in the stream. Since the surface waters in the area are used for agricultural purposes and for various leisure activities, it is necessary to make further detailed investigations into the extent of the metal pollution and to determine species, mobility and bioavailability of the metals.     

Rare earth elements in pore waters of marine sediments

The rare earth elements (REEs) were measured in pore waters of the upper ∼25 cm of sediment from one site off Peru and three sites on the California margin. The pore water REE concentrations are higher than sea water and show systematic down core variations in both concentration and normalized pattern. From these analyses and from comparison to other chemical species measured (dissolved Fe, Mn, Ba, oxygen, nitrate, phosphate), it is suggested that pore water REEs can be grouped into three categories: those that are from an Fe-source, those that are from a POC-source, and cerium oxide. REEs from the Fe-source appear where anoxia is reached; they have a distinctive “middle-REE (MREE) enriched” pattern. The concentrations in this source are so elevated that they dominate REE trends in the Fe-oxide reduction zone. The net result of flux from the POC-source is relative enrichment of heavy-REEs (HREEs) over light-REEs (LREEs), reflecting remineralizing POC and complexation with DOC. A common “linear” REE pattern, seen in both oxic and anoxic sediments, is associated with this POC-source, as well as a “HREE enriched” pattern that is seen in surficial sediments at the Peru site. Overall, the pore water results indicate that Mn-oxides are not an important carrier of REEs in the oceans.A REE biogeochemical model is presented which attempts to reconcile REE behavior in the water and sediment columns of the oceans. The model proposes that POC, Fe-oxide and Ce-oxide sources can explain the REE concentration profiles and relative abundance patterns in environments ranging from oxic sea water to anoxic pore water. The model is also consistent with our observation that the “Ce-anomaly” of pore water does not exceed unity under any redox condition.     

Factors controlling regional spatial distribution of 53 elements in coastal sea sediments in northern Japan: Comparison of geochemical data derived from stream and marine sediments

In all, 53 elements were analyzed in 1406 coastal sea sediment samples collected from an area off Hokkaido and the Tohoku region of Japan during 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 natural geochemical background variation and mass transport processes. The terrestrial area is covered by mafic volcanic rocks and accretionary complexes associated with ophiolite, which has small amounts of felsic volcanic rocks and granite. The spatial distribution patterns of elements enriched in mafic lithologies such as Fe (Total Fe₂O₃) and Sc in marine environments are influenced by adjoining terrestrial materials. The spatial distribution patterns of Cr and Ni concentrations, which are highly abundant in ultramafic rocks on land, are used to evaluate the mass transport from land to the sea and the dispersive processes caused by oceanic currents. The scale of mass transport by oceanic currents occurs up to a distance of 100–200 km from the coast along the coastal areas. The regional differences of elements rich in felsic lithologies such as K (K₂O), Nb and La in marine sediments are determined mainly by the relative proportion of minerals and lithic fragments enriching felsic materials to those associated with mafic materials. The spatial distribution of elemental concentration is not always continuous between the land areas and coastal sea areas. That difference is interpreted as resulting from (1) transportation of marine sediments by oceanic currents and storm waves, (2) contribution of volcanic materials such as tephra, (3) occurrence of shell fragments and foraminifera tests and (4) distribution of relict sediments of the last glacial age and early transgression age. Contamination with Cu, Zn, Cd, As, Mo, Sn, Sb, Hg, Pb and Bi was not observed in marine environments because the study area has little anthropogenic activity. Terrestrial materials are the dominant source for these metals. The Mo, Cd, Sn, Sb, Hg, Pb and Bi are abundant in silty and clayey sediments locally because of early diagenetic processes, authigenic precipitation and organic substances associated with these elements. The spatial distribution of As concentration shows exceptions: it is concentrated in some coarse and fine sands on the shelf. The enrichment is explained by adsorption of As, sourced from a coal field, to Fe hydroxide.     

Determination of some trace elements in geochemical standards by X-ray fluorescence

The following trace elements Cr, Cu, Nb, Ni, Pb, Rb, Sr, Y, Zn, and Zr were determined by X-ray fluorescence in some geochemical standards from Japan and France. The internal standard method was applied using a Philips PW 1410 X-ray spectrometer. The results were compared with the published data.     

海伦市土壤主要微量元素空间分布特征

以海伦市研究区1 175件表层(0~20 cm)土壤样品主要微量元素(B、Cu、Mn、Mo、Zn)的实测含量为研究对象,采用地统计学与GIS相结合的方法,对土壤微量元素的含量及空间分布特征进行分析。结果表明:研究区表层土壤中B和Mo含量较缺乏;Mn和Mo的块金效应大于75%,空间自相关性弱,B、Cu和Zn块金效应在25%~75%之间,属于中等空间相关,空间变异主要受到自然因素影响;B和Cu的空间分布相似,由中心向四周逐渐减少,Mn和Mo含量呈明显带状分布,Zn含量北部高于南部。微量元素之间既存在着共生关系,也可能存在拮抗关系。土壤有机质含量、成土母质、土壤类型和土地利用对微量元素均有不同程度的影响。     

Trace elements in surface sediments of Navarino Bay,Greece

The distribution of a number of trace elements in the Navarino Bay surface sediments is examined and their source and association with the major phases is determined. Cobalt follows Al in its distribution, having its highest vaues towards the center and deeper parts of the bay; Zn and Cu have their highest values at the effluent outfalls of a distillery and an olive oil and olive kernel factory (at the port of Yalova), being decreased away. The highest concentration of Ni is found near the town Pylos, while the highest concentrations of Rb and Y are observed at the mouths of rivers Yalovas and Xerias. Organic matter has its highest content at the port of Pylos, while no significant variations have been observed in the distribution of Sn and Ga. It is demonstrated that there is an anthropogenic input of Zn, Cu, and Corg in the bay. Zn and Cu are discharged by a distillery and an olive oil and olive kernel factory, at Yalova. Organic matter is mainly derived from domestic sewage. Ni enters the bay from its southern coasts and might be derived from weathering of bauxite deposits present in the adjacent limestones. Rb and Y are transported by the rivers Yalovas and Xerias from the northeastern adjacent land area; Ni, Co, and Cu show positive correlation with Al, suggesting their incorporation in clay minerals, while Rb shows positive correlation with Si, suggesting its incorporation in silicate detrital minerals. The following areas in the bay are considered to be heavily polluted: (1) the port and a large zone near Pylos (domestic sewage); (2) the port and a small area near Yalova (domestic sewage and industrial effluents); and (3) the eastern coast of the island Sphaktiria (oil). The domestic sewage pollution in Navarino Bay is of the same level as that in other Greek bays.