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1.
《Applied Geochemistry》2000,15(9):1369-1381
Thirty-eight samples of stream sediments draining high-grade metamorphic rocks in the Walawe Ganga (river) Basin, Sri Lanka, were analysed for their REE contents, together with samples of metamorphic suites from the source region. The metamorphic rocks are enriched in light REE (LREE) compared to heavy REE (HREE) and are characterised by high La/Lu ratios and negative Eu anomalies. The chondrite-normalised patterns for these granulite-grade rocks are similar to that of the average post-Archaean upper crust, but they are slightly enriched with La and Ce. The REE contents of the <63-μm fraction of the stream sediments are similar to the probable source rocks, but the other grain size fractions show more enriched patterns. The <63-μm stream sediments fraction contains lower total REE, more pronouncd negative Eu anomalies, higher EuN/SmN and lower La N/LuN ratios relative to other fractions. The lower La N/LuN ratio is related to the depletion of heavy minerals in the <63-μm fraction. The 63–125-μm and 125–177-μm grain size fractions of sediments are particularly enriched in LREE (average ΣLREE=2990 μg/g and 3410 μg/g, respectively). The total HREE contents are surprisingly uniform in all size fractions. However, the REE contents in the Walawe Ganga sediments are not comparable with those of the granulite-grade rocks from the source region of the sediments. The enrichment of REE is accounted for by the presence of REE containing accessory mineral phases such as zircon, monazite, apatite and garnet. These minerals are derived from an unknown source, presumably from scattered bodies of granitic pegmatites.  相似文献   

2.
 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  相似文献   

3.
This paper examines the surface sediments collected from Dongping Lake in China for speciation and distribution of toxic heavy metals (Cu, Pb, Ni, Cd) in different grain size fractions, and for the factors that need to be considered in potential hazard of metals to the environment. Four grain size fractions (<63, 63–78, 78–163 and 163–280 μm), divided in wet condition, and bulk samples less than 280 μm in diameter were analyzed for their distribution, density and appearance. A three-stage extraction procedure following the BCR protocol was used to chemically fractionate metals into “acid soluble”, “reducible”, “oxidizable” and “residual” fractions. Correlation analysis was used to analyze the datasets. The results showed that <63 μm grain size part constitutes the major proportion of the sediments, but its density is the smallest among the four grain size fractions. In general, the metal content curve against grain size presents “S” distribution, and the highest concentrations do not exist in <63 μm grain size. Appearance observation indicates that the adsorbed substance increases gradually along with the decreasing grain size. The dominant speciation of elements and the extent of pollution are responsible for the metal distribution in different grain size sediments. While studying bioavailability and mobilization of metals, it is advisable to take metal speciation, grain size distribution and density into consideration.  相似文献   

4.
 A total of 121 bed sediment samples were collected from a 5.8-km stretch of Manoa Stream, Hawaii. Samples were physically partitioned into two grain-size fractions, <63 μm and 63–125 μm, acid digested and analyzed by ICP-AES and FAAS. Non-parametric matched-pair statistical testing and correlation analysis were used to assess differences and strengths of association between the two fractions for Al, Ba, Cu, Fe, Mn, Ni, Pb, Ti and Zn. Results indicated statistically significant differences between fractions for all elements except Mn. Concentrations were significantly greater in the <63 μm fraction for Al, Cu, Pb, Ti and Zn, while Ba, Fe and Ni were higher in the 63–125 μm fraction. Though some elements had statistically significant differences between fractions (Al, Ba, Fe and Zn) percentage differences were in the range of analytical precision of the instrument and thus differences were not practically significant. Correlation analysis indicated strong positive associations for all elements between the two fractions (p<0.0001). Three contamination indices indicated similar degrees of pollution for each size fraction for four elements having an anthropogenic signal (Ba, Cu, Pb and Zn). The environmental information obtained from the 63–125 μm fraction was essentially equivalent to that from the <63 μm fraction. In this system it is clear that both bed sediment fractions indicate anthropogenic enrichment of trace metals, especially Pb, and further supports previous research that has found that aquatic sediments are critical median for tracing sources of pollution. Received: 17 August 1998 · Accepted: 30 October 1998  相似文献   

5.
Urban roadside soils are important environmental media for assessing heavy metal concentrations in urban environment. However, among other things, heavy metal concentrations are controlled by soil particle grain size fractions. In this study, two roadside sites were chosen within the city of Xuzhou (China) to reflect differences in land use. Bulk soil samples were collected and then divided by particle diameter into five physical size fractions, 500–250, 250–125, 125–74, 74–45, < 45 μm. Concentrations of metals (Ti, Cr, Al, Ga, Pb, Ba, Cd, Co, Cu, Mn, Ni, V, Zn, Mo, As, Sb, Se, Hg, Bi, Ag) were determined for each individual fraction. These metals could be roughly classified into two groups: anthropogenic element (Pb, Ba, Cd, Cu, Zn, Mo, As, Sb, Se, Hg, Bi, Ag) and lithophile element (Ti, Cr, Al, Ga, Co, Mn, Ni, V) in terms of values of enrichment factor. As expected, higher concentrations of anthropogenic heavy metals (Cu, Zn, Mo, As, Hg, Bi, Ag) are observed in the finest particle grain size fraction (i.e. < 45 μm). However, heavy metals Se, Sb and Ba behave independently of selected grain size fractions. From the viewpoint of mass loading, more than 30% of the concentrations for all anthropogenic heavy metals are contributed by the particle grain size fractions of 45–74 μm at site 1 and more than 70% of the concentrations for all heavy metals are contributed by the particle grain size fractions of 45–74 and 74–125 μm at site 2. These results are important for transport of soil-bound heavy metals and pollution control by various remedial options.  相似文献   

6.
 The Oka River basin is located in the Urdaibai National Biosphere Reserve, North Spain. In order to obtain a preliminary view of its environmental conditions, nitric acid extractable Fe, Mn, Zn, Pb, Cu, Cr, Ni and Co, organic matter content (L.O.I.), geochemical fractionation of heavy metals and mineralogical composition were analysed in surficial sediments (fraction <63 μm) collected in October 1991. Relatively high concentrations of metals occurred in a sampling site upstream, due to a local natural enrichment controlled by weathering of volcanic rocks. Geochemical fractionation confirmed the lithogenic origin of metals, which were mainly associated to the detrital phase. The significant increase of heavy metals found in some samples collected in the municipal area of Gernika suggested a pollution effect, related to anthropogenic wastes. Large amounts of metallic slags have been found mixed with the sediments upstream from this locality. Nevertheless, in view of their composition, it is unlikely that these slags constitute a significant source of heavy metals in the studied area. In a second sampling in October 1997 an apparent decreasing trend in some heavy metal levels was noted, particularly for Pb and Cu. Nowadays, enrichment factors relative to background values confirm moderate anthropogenic influence on Zn, Pb, Cu, Cr and Ni concentrations. However, heavy metal levels in the Oka river sediments are much lower than those detected in other major rivers of the Basque Country (Nervión, Urumea, Deba). Received: 7 July 1997 · Accepted: 4 July 1998  相似文献   

7.
Heavy metal distribution in sediments of Krishna River basin,India   总被引：1，自引：0，他引：1  
Suspended and bed sediments collected from the entire region of the Krishna River and its major tributaries were analyzed for heavy metals (V, Cr, Mn, Fe, Co, Ni, Cu, Zn, and Pb) by the thin-film energy dispersive x-ray fluorescence technique. There is considerable variation in the concentration of elements towards downstream, which may be due to the variation in the subbasin geology and various degrees of human impact. Suspended particles are enriched in heavy metals throughout the basin relative to bed sediments. The heavy metals are enriched in coarse size fractions (10–90 µm) throughout the Krishna River except its tributary Bhima, where finer fractions (2 µm) dominate. Transition elements correlate very well with each other. There is a striking similarity between the bed sediments of Krishna River and the Indian average. When the annual heavy metal flux carried by the Krishna River was estimated, and viewed in relation to the other major riverine transport, the Krishna is seen to be a minor contributor of heavy metals to the Bay of Bengal.  相似文献   

8.
 The distribution of Si, Al, Fe, Mn, Cu, Zn, Ni and Cr in different grain-size fractions and geochemical association of Fe, Mn, Cu and Zn with <63-μm size fraction of bed sediments of Damodar River has been studied. In general, concentrations of heavy metals tend to increase as the size fractions get finer. However at two sites, near mining areas, the coarser particles show similar or even higher heavy metal concentrations than finer ones. The higher residence time and/or presence of coarser particles from mining wastes are possibly responsible for higher metal content in the coarser size fractions. The chemical fractionation study shows that lithogenic is the major chemical phase for heavy metals. Fe and Mn are the major elements of the lithogenic lattice, constituting 34–63% and 22–59%, respectively, of total concentrations. Fe-Mn oxide and organic bound fractions are significant phases in the non-lithogenic fraction. The carbonate fraction is less significant for heavy metal scavenging in the present environment and shows the following order of abundance Zn>Cu>Mn>Fe. The exchangeable fraction of the Damodar sediments contains very low amounts of heavy metals suggesting poor bioavailability of metals. Received: 18 August 1998 · Accepted: 1 December 1998  相似文献   

9.
Road dust collected from India’s richest and oldest coal mining belt of Dhanbad and Bokaro regions was analysed for particle size characteristics and elemental composition. The particle size distribution pattern shows dominance of 500–250 μm and 250–125 μm size fractions, constituting 45–58% of the mass size spectrum. Si is the most dominant element and its concentration varied between 29.3 and 36.4% with the average value 34.3%. Fe, Ti and Mn are the dominant heavy metals followed by Zn, Cr, Pb, Cu, Ni and Co. No significant differences concentration of metals between sampling sites was apparent; however, some sites tend to accommodate relatively higher metals due to its proximity to industrial and mining sites. In general, finer fraction (<63 μm) tend to contain 1–3 times higher metals as compared with the bulk composition. Except Pb and Mn all the measured metals are generally lie below grade zero, suggesting that there is no pollution threat with respect to these metals in roadway dust from the studied sites. Geochemical speciation study shows that the lithogenic phase is the major sink for heavy metals. Fe–Mn oxide and organic are the major non-lithogenic phases and Pb and Zn are the major elements of the non-lithogenic phase.  相似文献   

10.
 The Ganga Plain is one of the most densely populated regions and one of the largest groundwater repositories of the Earth. For several decades, the drainage basin of the Ganga Plain has been used for the disposal of domestic and industrial wastes which has adversely affected the quality of water, sediments and agricultural soils of the plain. The concentrations of Al, Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, Sn, Zn and organic carbon were determined in river sediments and soils of the Ganga Plain in the Kanpur-Unnao industrial region in 1994 and 1995 (pre-monsoon period of April–May). High contents (maximum values) of C-org (12.0 wt. %), Cr (3.40 wt. %), Sn (1.92 wt. %), Zn (4000 mg/kg), Pb (646 mg/kg), Cu (408 mg/kg), Ni (502 mg/kg) and Cd (9.8 mg/kg) in sediments (<20 μm fraction); and C-org (5.9 wt. %), Cr (2.16 wt. %), Sn (1.21 wt %), Zn (975 mg/kg) and Ni (482 mg/kg) in soils (<20 μm) in the pre-monsoon period of 1994 were found. From 1994 to 1995 the contents of Fe and Sn in sediments increase whereas those of C-org, Cd, Cu, Ni and Zn decrease. Considering the analytical errors, Al, Co, Cr, Mn and Pb do not show any change in their concentrations. In soils, the contents of Cd, Fe and Sn increase whereas those of Ni decrease from 1994 to 1995. Aluminium, Co, Cr, Cu, Mn, Pb and Zn do not show any change in their concentrations from 1994 to 1995. About 90% of the contents of Cd, Cr and Sn; 50–75% of C-org, Cu and Zn; and 25% of Co, Ni and Pb in sediments are derived from the anthropogenic input in relation to the natural background values, whereas in soils this is the case for about 90% of Cr and Sn; about 75% of Cd; and about 25% of C-org, Cu, Ni and Zn. The sediments of the study area show enrichment factors of 23.6 for Cr, 14.7 for Cd, 12.2 for Sn, 3.6 for C-org, 3.2 for Zn, 2.6 for Cu and 1.6 for Ni. The soils are enriched with factors of 10.7 for Cr, 9.0 for Sn, 3.6 for Cd, 1.8 for Ni and 1.5 for Cu and Zn, respectively. Received: 3 March 1998 · Accepted: 15 June 1998  相似文献   

11.
Bed sediment-associated trace metals in an urban stream, Oahu, Hawaii   总被引：78，自引：0，他引：78  
 Of the 117 stream and lake systems sampled nationwide, fish from Manoa Stream on Oahu, Hawaii, have consistently shown the highest Pb concentrations. Therefore a detailed study was conducted to examine total metal contents in bed sediments from a 5.8-km stretch of Manoa Stream. A total of 123 samples (<63 μm) were examined for 18 elements and 14 samples for 21 elements. Selected samples were also examined using different leach solutions to examine metal phase associations. All trace metal data, computations of enrichment ratios and the modified index of geoaccumulation point to mineralogical control for Cr and Ni; minor anthropogenic contamination for Ba, Cd, Cu, Hg and Zn; and a very strong contamination signal for Pb. Maximum Pb contents (up to 1080 mg kg−1) were associated with anthropogenic material dumping in minor tributaries, storm sewer sediments and sediments in the “lower” section of the basin. Proportionally Pb had the highest non-residual component of elements examined; dominantly in the reducible phase associated with Mn and amorphous Fe oxyhydroxides. The contamination signal was typically lowest in the “undisturbed” headwater reach of the basin (above 5.1 km) with significant increases throughout the “residential” and “commercial-institutional” zones of the mid-basin. The spatial pattern of bed sediment contamination and evidence from storm sewer-outlet sediments strongly indicates that Pb, and to a lesser degree some other metals, is still being transported to the stream and the primary agent is soil erosion and transport of metals sorbed to sediments. The primary source of sediment-associated metals is considered to be the automobile, though other minor sources can not be ruled out. Received: 3 November 1998 · Accepted: 26 January 1999  相似文献   

12.
 Size-normalized (<63 μm) distributions of Cu, Zn, and Pb in the surficial sediments of one of Sydneys' four major estuaries – the Georges River/Botany Bay estuary – are not facies or depositionally controlled, but rather their distribution is dominated by source. Point sources (waste dumps, sewage overflows, and discharge from a polluted river) are responsible for elevating sediment heavy-metal concentrations up to 50 times above background. Nonpoint sources contribute in raising baseline levels to four times background and comprise mainly stormwater and also marinas, moorings, and wharfs/jetties. Heavy metals disgorged from a point source (Cooks River) strongly impact the sediments in the lower estuary, which has implications for the construction of a new runway for Sydney airport. Received: 3 October 1994 · Accepted: 21 September 1995  相似文献   

13.
The abandoned Kilembe copper mine in western Uganda is a source of contaminants, mobilised from mine tailings into R. Rukoki flowing through a belt of wetlands into Lake George. Water and sediments were investigated on the lakeshore and the lakebed. Metal associations in the sediments reflect the Kilembe sulphide mineralisation. Enrichment of metals was compared between lakebed sediments, both for wet and dry seasons. Total C in a lakebed core shows a general increment, while Cu and Co decrease with depth. The contaminants are predominant (> 65%) in the ≤ 63 μm sediment size range with elevated Cu and Zn (> 28%), while Ni, Pb and Co are low (< 18%) in all the fractions. Sequential extraction of Fe for lakeshore sediment samples reveals low Fe mobility. Relatively higher mobility and biological availability is seen for Co, Cu and S. Heavy metal contents in lake waters are not an immediate risk to the aquatic environment.  相似文献   

14.
《Applied Geochemistry》2001,16(3):339-350
This study on the application of multi-element relationships in stream sediments to mineral exploration in the Walawe Ganga Basin presents one of the first of its kind in Sri Lanka. In order to determine the nature of these sediments, multi-element analysis of selected grain size (<63 μm, 63–125 μm, 125–177 μm and 177–250 μm) fractions was undertaken. The chemical composition of these fractions were compared with those of the upper continental crust.Some elements, notably Zr, Hf, Th, U, Ce and La, show very high enrichment factors (e.g. 54 for Zr) as compared to the upper crustal abundance. These are presumably associated with heavy minerals such as zircon, rutile and monazite found in abundance in the stream sediments of the Walawe Ganga Basin.Principal Component Analysis (PCA) of the geochemical data show that multi-element relationships could be effectively used to delineate target areas for mineral exploration. With the use of PCA, this study reveals that areas with associations of calc-silicate/marble and charnockitic rocks are probable source regions for mineral occurrences, particularly in the axial regions of anticlines.  相似文献   

15.
《Applied Geochemistry》1996,11(4):605-616
Lake Valencia is a tropical lowland lake in north-central Venezuela. Lake bottom sediments were collected from 25 locations in April, 1988. At 2 locations water pH, conductivity, dissolved O2 and temperature were measured at successive depths. After drying, 5 sediment samples were sieved into 5 mechanical fractions. Each was extracted with 1 M HNO3 and analysed for AI, Ca, Cd, Co, Cr, Cu, Fe, K, Mg, Mn, Na, Ni, Pb and Zn. The <63 μm fraction of all samples was similarly analysed. Water temperatures declined with depth (1°C/25 m) from approximately 26°C. Conductivity varied little with depth but dissolved O2 contents indicated anoxic conditions < 25 m. Water pH (8.8–9.4) was consistent with high dissolved carbonates. There was little consistent relationship between grain size and sediment metal contents. Approximate baseline metal contents were calculated from 21 of 25 samples. The average composition of the sediments corresponded to an ideal mixture of shales/carbonate rocks as 0.5–0.7/0.5-0.3. Five samples from alluvial fans near the mouths of rivers traversing urban-industrial zones had compositions different from the other sediments. Generally, Ph, Zn, Ni, Cd and Cu were anthropogenically enriched by factors of 2–16. The major sources of pollutants were identified as domestic and industrial activities affecting the rivers that traverse the lakeside cities of Maracay and Valencia. Sodium, Mg, Ca, Mn and CO3− showed natural enrichment arising from carbonate precipitation following a physical mixing of 2 sedimentary components (biogenic carbonate and terrigenous material). Low geochemical mobility of metallic elements in neutral-basic and reducing waters, a processes of bury and mixture of sediments and precipitation of carbonate result in only 10% of the lake area being affected by contamination. Isoline plots of elements in the bottom sediments supported a hypothesis that material mixing, physical transport and carbonate precipitation are the main controls of spatial distribution patterns.  相似文献   

16.
Analysis of 3-m sediment cores revealed that profiles of carbon (C), sulfur (S), and iron (Fe) varied with relative distance from marine and terrestrial sediment sources in Tomales Bay California. Despite relatively high sedimentation rates throughout the bay (historically 3–30 mm yr−1), sulfate reduction of deposited organic matter led to free-sulfide accumulation in sediments only at the location farthest from terrestrial runoff, the source of reactive iron. Acid-volatile sulfide concentrations in all sediments (<10 μmol g−1) were low relative to concentrations of chromiumreducible sulfide (up to 400 μmol g−1 farthest from the reactive iron source). A calculated index of iron availability, used to describe sediment resistance to build-up of free sulfide, was lowest at this location. Recent, upward shifts in reactive Fe concentration and in the relative contribution of terrestrial orgnic carbon (measured as a shift in δ13C of bulk sediment organic matter) in all cores indicated that erosion and transport of sediments from the watershed surrounding Tomales Bay increased after European settlement in the 1850s.  相似文献   

17.
 Distribution of the trace elements Cr, Cu, Ni, Pb and Zn in surficial sediments of the river/sea environment in Danang – Hoian area (Vietnam) was investigated to examine the degree of metal pollution caused by anthropogenic activities. Point sources from domestic and industrial wastes are identified as dominant contributors of trace element accumulation. Surficial sediments of Hoian River show extremely high total concentrations of Cu (Average Concentration 295 μg/g), Ni (AC 112 μg/g), Pb (AC 396 μg/g) and Zn (AC 429 μg/g) that exceed assigned safety levels ER-M. Similarly, the sediments of Han River show high Pb (AC 188 μg/g) and Zn (AC 282 μg/g) contents. In marine sediments of Thanhbinh beach Pb is also enriched (138 μg/g) above guideline levels. In contrast the sediments of the Cude River are dominated by trace element concentrations close to background values. Received: 17 December 1998 · Accepted: 6 May 1999  相似文献   

18.
Dry lakes, degraded sandy grasslands, abandoned farmland and mobile dunes which are widely distributed throughout the arid areas of northern China have been investigated in this work. Gain-size distribution of the surface sediments of Manas lake in Junggar basin, Juyan lake in the Alxa plateau, Zhuye lake in Minqin basin and most deserts (such as Mu Us desert, Otindag desert, Horqin desert and Hulun Buir desert) in China have been analyzed. The results show clay with particle sized <10 μm on the surface sediments of dry lakebed and sandy grassland developed from dry lakebed, respectively, account for >60% and ∼50% of the total mass. Since the tiny particles on the surface of abandoned farmland are blown away easily and rapidly, the content of clay particles in Minqin basin is <14%. The grain-size distribution of mobile dunes in northern China mainly consists of particles >63 μm and few particles <10 μm. Consequently, although sand/dust storms originate primarily in the western deserts, the gobi areas of the Alxa plateau, the north and east of Hexi Corridor and in central Mongolia, the widely distributed dry lakebeds, sandy grasslands and abandoned farmland adjacent to the deserts also contribute to aeolian dusts. Hence, the material sources for sand dust storm in East Asia include inland deserts, but also dry lakes, sandy grasslands and abandoned farmland, which are widely distributed throughout the arid inlands of northern China.  相似文献   

19.
A conceptual isotopic/geochemical model is presented to explain the variation of major, trace and rare earth element (REE) geochemistry and Sr isotope systematics in suspended particulate matter (SPM) as a function of particle/colloid size. This conceptual model is an extension of a previous investigation of the origin of SPM in the Murray-Darling River system (MDRS) that utilised Sr isotope systematics to examine aspects of SPM (particle/colloid) origin, structure and mineralogy. The geochemical processes that give rise to the often coherent trends in major, trace and REE geochemistry and Sr isotopic signature as a function of particulate (<1 μm) and colloidal (>1 μm) size in the MDRS have been identified using an enhanced SPM size fractionation technique as a basis to not only obtain a broad range of particle/colloid size ranges, but also to provide sufficient material for subsequent geochemical and isotopic analysis. The conceptual isotopic/geochemical model proposed here contains three major components: (i) the differential weathering of micas and alkali (K-) feldspars to form the majority of the particulate (<1 μm) fractions (high 87Sr/86Sr ratio), which have a geochemical and Sr isotopic signature that closely resembles precursor mineralogies, (ii) the differential weathering of Na, Ca-feldspars (plagioclase) which decompose to form clay minerals in the colloidal (>1 μm) fractions (low 87Sr/86Sr ratio), with a range of geochemical signatures related to the relative proportions of inorganic and organic constituents, and (iii) the presence of natural organic matter as coatings on the particulate (<1 μm) and colloidal (>1 μm) matter and possibly as organo-colloids which exert an increasing influence in particular on bulk colloid geochemistry with decreasing colloid size. This conceptual isotopic/geochemical model also accounts for the distinct variation in major, trace and REE geochemistry and Sr isotopic systematics between the particulate (<1 μm) and colloidal (>1 μm) fractions, the variation being primarily a function of the distinctly different precursor mineralogies of the SPM fractions and geochemical fractionation during the weathering and transport. Additionally, this model explains a systematic fractionation of REE apparent within colloidal (>1 μm) fractions. Statisitcal (hierachical cluster) analysis of two particulate and three colloidal fractions from 23 samples from the MDRS is used as a basis to investigate geochemical and mineralogical associations within the particulate and colloidal size fractions and to provide additional supporting evidence for the conceptual isotopic/geochemical model. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

20.
Surficial sediment samples were collected at 47 stations in Little Traverse Bay, Lake Michigan, to determine the geochemical associations between certain rare earth elements (REE's) and trace metals. Each sample was analyzed for carbonate carbon, organic carbon, grain size, and the elements Al, Ca, Ce, Co, Cr, Eu, Fe, Hf, La, and Mn. Two distinct Ce subpopulatins were identified by graphical analysis, and an R-mode factor analysis was applied to data from the “enriched” Ce subpopulation (18 samples). Results show that the REE's and trace metals are primarily enriched in the authigenic phase of these sediments. Partial correlation analyses indicate that the REE's are primarily associated with hydrous Fe oxides relative to organic matter in this phase. The ratio of Ce/La concentrations increased markedly from the bay margins to the central trough of the bay, indicating that Ce, similar to Fe, exhibits a variable oxidation state in the authigenic phase of nearshore fine-grained sediments. The results of the present study suggest that the REE's and trace metals behave coherently in the authigenic phase of recent lacustrine sediments, and the REE's may be useful as geochemical tracers to differentiate between trace metal enrichments in surface sediments as a result of diagenesis and pollution loadings.  相似文献   

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