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1.
《Applied Geochemistry》2001,16(1):123-136
Concentrations of several elements extractable with BaCl2 and acid ammonium acetate (pH 4.65) were measured in the organic and 4 mineral soil layers on the national forest inventory plots of the Finnish Forest Research Institute. The soil data also includes total concentrations of elements in the organic layer and site and soil physical characteristics. Data were compared with the aqua regia extractable element concentrations measured in the nationwide regional till geochemical mapping carried out by the Geological Survey of Finland.Correlations between concentrations in surface soil and underlying basal till were generally highest for K, Mg, Mn, P and Zn; in the organic layer and till they were highest for Cr and Cu. The strength of these correlations did not increase regularly from surface to deeper soil layers. All soil base cations with the exception of Ca, which is of relatively low solubility, were well correlated. The elements Zn, K, P, Al and Mn in till were the most reliable indicators of surface soil chemistry.Fuzzy clustering showed that the correlation between element concentrations in basal till and the two uppermost layers of mineral soil was better within areas of distinct till geochemistry, such as the schist belts in southwestern Finland, the Lake Ladoga–Bothnian Bay zone and the Kuusamo schist belt.Surface soil chemical variables were clearly better in discriminating fertility classes of forest sites than were element concentrations in basal till. The independent ability of till geochemistry to distinguish these productivity classes and to explain surface soil fertility was nevertheless demonstrated. 相似文献
2.
Dominik Weiss William ShotykJack Rieley Susan PageMarlies Gloor Steve ReeseAntonio Martinez-Cortizas 《Geochimica et cosmochimica acta》2002,66(13):2307-2323
Biogeochemical processes in a forested tropical peat deposit and its record of past atmospheric dust deposition were assessed using the vertical distribution of lithophilic and plant essential elements in a dated core profile from Borneo, SE Asia. Peat formation started ∼22,120 14C yr before present (BP), and Ca/Mg mass ratios of the solid peat and very low ash contents indicate a strongly ombrotrophic character throughout the deposit, implying that most of the inorganic fraction has been supplied exclusively by atmospheric inputs. Concentration profiles of Mn, Sr, and Ca suggest a very minor influence of chemical diagenesis in the underlying sediments. Silicon, Ca, Mg, P, S, and K show a strong and extended zone of enrichment in the top 200 cm of the profile, indicating that biological accumulation mechanisms are much more extensive than in temperate peat bogs.In the lower core sections, where the element distribution is dominated solely by past atmospheric deposition, average Al/Ti ratios are similar to the upper continental crust (UCC), whereas Fe is slightly enriched and Si is strongly depleted: this condition favors highly weathered tropical soil dust as the main inorganic mineral source. Significant correlation of Al, Fe, Si, S, Ca, and Ti with the lithophilic elements Y and Zr suggests that the distribution of these elements is controlled by sources of atmospheric mineral dust. The Ca/Mg, Ca/K, and Mg/K ratios of the collected rainwater samples are similar to the global average of continental rainwater and suggest a continental character for the site. This is supported by the similarity of the average concentration of Br, Mg, Ca, and S to that in temperate continental and maritime bogs in Switzerland and Scotland.The concentration profiles of Si, Fe, Al, and Ti show distinct peaks within the profile, implying enhanced dust deposition, reduced rates of peat accumulation, or possibly both owing to climatic changes during the Holocene. Enhanced dust deposition between ∼10,830 and 9060 14C yr BP is tentatively interpreted as a Younger Dryas-like event with dust fluxes of ∼10.8 mg/m2/yr. The variations in Al/Ti and Fe/Ti profiles suggest that mineral dust sources have been changing constantly during the Holocene, with local sources being dominant between ∼7820 and 9500 14C yr BP and long-range transport (derived most likely from China) being important during the late Pleistocene and early Holocene and from ∼7820 14C yr BP to the present. 相似文献
3.
Metal concentrations from stream waters in two geological blocks in Northern Ireland were compared to determine the contributions of catchment characteristics and in-stream conditions. One block is composed of metamorphosed schist and unconsolidated glacial drift with peat or peaty podzol (mainly humic) soils, while the other block consists of tertiary basalt with brown earth and gley soils. Water samples were collected from 52 stream sites and analysed for iron (Fe), manganese (Mn) and aluminium (Al) as well as a range of other chemical determinands known to affect metal solubility. Densities of metal-rich ochre deposit were determined for stream bed stone samples. Higher conductivities and concentrations of bicarbonate, alkalinity, calcium and magnesium occurred on basalt than on schist. Despite higher Fe and Mn oxide concentrations in basalt-derived non-humic soils, stream water concentrations were much lower and ochre deposit densities only one-third of those on schist overlain by humic soils. Neither rock nor soil type predicted Al concentrations, but pH and dissolved oxygen did. Peat-generated acidity and the limited acid neutralising capacity of base-poor metamorphosed schist have resulted in elevated concentrations of metals and ochre deposit in surface waters. 相似文献
4.
Pertti W. Lahermo 《Environmental Geology》1991,18(1):57-69
About 6,400 water samples were collected from small catchments in northern Finland and Norway above 66° N latitude as a part of the Nordkalott Project carried out jointly by the Geological Surveys of Finland, Norway, and Sweden. Electrical conductivity (EC) was measured in situ and Ca, Mg, Sr, Ba, Na, K, Si, Fe, Mn, Al, and Zn concentrations were determined from filtered and acidified samples by the ICAP method. The relative abundance of mafic, ultramafic, and carbonate rock components in the catchments is the most influential factor controlling the EC values and the main cation concentrations (Ca, Mg, Sr). These components also determine the HCO3 alkalinity or acid-neutralizing capacity (ANC) of streamwater. In the northern coastal belt, Na is derived largely from airborne sea salts, but in the southwestern corner of the research area it may be derived partly from relict sea salts in sediments. The concentrations of Na, K, and Si do not depend solely on the lithological environment. Fe and, to a lesser extent, Mn and Al occur in the highest abundances in the low-lying, intensely paludified southern part of the area, suggesting that these metals tend to go into solution and are transported in complexed forms with dissolved and colloidic humic matter. The areal distribution patterns of the main cations (Ca, Mg, Sr) and of some heavy metals (Fe, Mn) in streamwater are fairly consistent with those of till and minerogenic stream sediments, although, in a statistical approach, only a few significant correlation coefficients were established. 相似文献
5.
This study assesses a simple sediment source tracing method using major- (Al, Ca, Fe, K, Mg, Mn, Na, P, Si, Ti) and trace-element (Ba, Be, Ce, Co, Cr, Mo, Nd, Pb, Sr, Th, V, Y, Zn) signatures of stream suspended particulate matter (SPM), bed sediments and soils in a small agricultural catchment in NE Scotland. Whilst most erosion studies characterise the large amounts of material mobilised at the highest flows, this study aimed to assess properties of sediments during moderate to low flow periods. These occur more frequent than intense storms and are important in linking stream sediments, near-channel sources and aquatic ecosystem impacts. Data were transformed by multivariate statistical methods to compare elemental signatures of SPM (ranging from 3 to 53 mg L−1 in the stream) and stream bed sediments with a limited number of near-channel source soils. Increased concentrations of Ce, Nd, Th and Y in subsoils contributed to the ability to discriminate between surface fieldslope and stream bank erosion sources. Stream bed sediments showed close matches with compositions of stream bank and arable surface soils, but signatures of SPM differed greatly from any of the sources. Large concentrations of Cr, Pb and Zn in SPM, particularly during summer (677, 177 and 661 mg kg−1, respectively) exceeded water quality standards and were linked to an accumulation of trace elements associated with biological material. The potential for within-stream alteration of SPM in relation to erosion sources was confirmed by changes in the nature of the SPM organic matter observed by IR spectroscopy. Thus the potential is shown for multi-element signatures to give information on catchment sediment sources to aid land management decisions, given careful consideration of the effects of in-stream alteration of eroded material. However, this combined information may be beneficial to process understanding linking land use and stream ecosystems at critical ecological periods. 相似文献
6.
Water and bed sediment samples collected from the Damodar River and its tributaries were analysed to study elemental chemistry
and suspended load characteristics of the river basin. Na and Ca are the dominant cations and HCO3 is the dominant anion. The water chemistry of the Damodar River basin strongly reflects the dominance of continental weathering
aided by atmospheric and anthropogenic activities in the catchment area. High concentrations of SO4 and PO4 at some sites indicate the mining and anthropogenic impact on water quality. The high concentration of dissolved silica,
relatively high (Na+K)/TZ+ ratio (0.2–0.4) and low equivalent ratio of (Ca+Mg)/(Na+K) indicate that dissolved ions contribute significantly to the weathering
of aluminosilicate minerals of crystalline rocks. The seasonal data show a minimum ionic concentration in the monsoon season,
reflecting the influence of atmospheric precipitation on total dissolved solids contents. The suspended sediments show a positive
correlation with discharge and both discharge and suspended load reach their maximum value during the monsoon season. Kaolinite
is the mineral that is possibly in equilibrium with the water. This implies that the chemistry of the Damodar River water
favours kaolinite formation. The concentration of heavy metals in the finer size fraction (<37 μ m) is significantly higher
than the bulk composition. The geoaccumulation index values calculated for Fe, Mn, Zn, Ni and Cr are well below zero, suggesting
that there is no pollution from these metals in Damodar River sediments.
Received: 21 January 1998 · Accepted: 4 May 1998 相似文献
7.
《Applied Geochemistry》1997,12(5):593-605
The impact of sediment type on stream water geochemistry was studied in a catchment in Finland affected by sulphidic fine-grained sediments. Stream water samples for general characterisation of water quality (pH, electrical conductivity) were taken at the basin outlet during various hydrological conditions, while samples for detailed geochemical analysis were collected at 119 sites in the catchment on one single occasion during high-water flow in autumn. The occurrence of sulphidic fine sediments was estimated based on data from an airborne electromagnetic survey carried out by the Geological Survey of Finland.Growing-symbol maps, which were prepared for each of the studied variables in water, and statistical calculations including factor analysis and Spearman correlations show that the concentrations of Al, Ga, U and Tl, all the lanthanides and several alkali and alkaline earth metals (K, Mg, Na, Li, Ca, Rb, Sr), transition metals (Cd, Co, Cu, Zn, Sc, Mn, Ni, Y, Hf) and non-metals (S, Br, I, Si) increase in water when the proportion of the catchment cover of sulphidic fine sediments increases. It is therefore argued that these elements are released and mobilised in considerable amounts by the oxidation and subsequent acidification and weathering of this type of sediment. Other elements are either slightly depleted in streams in areas of sulphidic fine sediments (V, Nb, Pb, Zr), have a distribution unrelated to sediment type (Fe, Cr, Cs, Mo), or are only weakly impacted by the occurrence of sulphidic sediments in the catchment (As, Ti, Ba). It is argued that these elements are not leached extensively from the oxidising sulphidic sediments, and that their distributions at least partly may be controlled by the contents of dissolved humic material and/or suspended organic and inorganic phases in the water. 相似文献
8.
东营凹陷古近系中深层湖盆演化中的无机元素响应 总被引：2，自引：1，他引：1
为查明无机元素分布与水深、盐度等沉积环境以及湖盆演化过程的关系,采用电感耦合等离子体发射光谱仪分析对东营凹陷郝科1科探井古近系深层微量元素含量进行了测试、分析,所涉及的研究层位是该凹陷的主要烃源岩层段（沙河街组三亚段、沙河街组四亚段、孔店组）,分析结果表明:在水体浅、蒸发作用强烈的孔店组—沙四下亚段强氧化性滨浅湖环境里,钙、锶含量和Ca/Mg、Sr/Ba、Sr/Ca参数值具低值响应,铁、铝、钡、钒含量和（Fe+Al）/(Ca+Mg)参数值具高值响应;在沙四中亚段膏岩、盐岩等普遍发育的盐湖环境中,钠、锶含量和Sr/Ba、Fe/Mn、Sr/Ca均出现高值响应,锰、钡、钒含量和V/Ni、(Fe+Al)/(Ca+Mg)出现低值响应;在还原性的沙四上亚段半咸化深湖环境中,钾、钠、铁含量和Fe/Mn值具低值响应,钙、锰含量具高值响应;在沙四中亚段膏盐与泥岩共生体系中元素分布离散性明显,呈现波动性特征;Sr/Ba、Sr/Ca在盐湖环境中出现显著的高值响应,被证实可以作为良好的水体盐度指标参数,Fe/Mn、(Fe+Al)/(Ca+Mg)随水体加深逐渐增大,是良好的水体深浅指标参数。元素分布受沉积环境、岩性特征等多种地质因素的影响,在利用元素含量分布及特征元素比值来判断某单个地质因素的变化时,应该应用多种参数,进行综合判断。 相似文献
9.
Four overbank profiles from the three terraces of different age were sampled in 10 to 20 cm intervals for the bulk content of major and minor (Ca, Mg, Fe, Ti, Al, Na, K and P) and trace (Mo, Cu, Pb, Zn, Ni, Co, Mn, As, U, Th, Sr, Cd, Sb, V, La, Cr, Ba, W, Zr, Ce, Sn, Y, Nb, Ta, Sc, Li, Rb and Hf) elements in the minus 0.125 mm fraction. Univariate statistics together with analysis of variance discriminated between the lower-lying carbonate (CA) population dominantly composed of carbonates and the overlying silicate (SI) population being dominantly of silicate mineralogy. This stratified pattern resulted from the intensive erosive action of melting glaciers exerted on limestones and dolomites in the alpine region, followed by local inputs mainly of silicate composition. Elements exhibiting the greatest between-population variability are Ca and Mg being enriched in the CA population and Fe, Mn, P, Sr, Al, Na, K, Li, Rb, Y, Zr, Ni, Cr and Ti being enriched in the SI population. Anomalously high Hg, Pb and Ba concentrations (maximum values: 6,500±2,860 ppb, 225±13 ppm and 1,519±91 ppm, respectively) in the lowermost part of the profile S7, which is nearest to the Croatian-Slovenian border, derive from the mineralized Slovenian catchment area. This profile also contains trimodal frequency distributions of Fe, Mn and P whose highest concentrations coincide with increased values of Zn and Cu which are bimodally distributed. Geochemical patterns of majority of elements in all four profiles consistently reflect the average compositions of the upstream drainage basins. 相似文献
10.
Abundance, Sources and Speciation of Trace Elements in Humus-Rich Streams Affected by Acid Sulphate Soils 总被引：3，自引：0，他引：3
The behaviour of trace elements (Al, As, Cd, Co, Cr,Cu, Fe, Mn, Ni, V, Zn) was studied in five humus-richstreams (dissolved organic carbon = 14–40 mg/L)impacted by acid sulphate soils developed in marinesulphide-bearing fine-grained sediments. During heavyrainfalls in autumn, on which the study focusses, themetals Al, Cd, Co, Cu, Mn, Ni and Zn are extensivelyleached from these acidic soils (pH = 2.5–4.5), whileAs, Cr, Fe and V are not leached more strongly fromthis soil type than from areas of till and peat. Aspeciation experiment, based on anion and cationexchange of the stream waters in the field, showedthat (1) the metals Al, Cd, Co, Mn, Ni and Zn aretransported in the streams mainly as inorganiccations, (2) Cu exists mainly in cationic form but isalso to a significant extent associated with dissolvedhumic substances, (3) Fe occurs mainly in the anionicfraction explained by organic coating on colloidal Feoxyhydoxides and (4) the hydrochemistry of As, Cr andV is complex as these elements may exist in severalunquantified anionic fractions and to a minor extentin cationic species/forms. Whereas the proportion ofacid sulphate soils in the catchments had a largeimpact on concentrations levels of several elements inthe stream waters, these soils did not have a largeaffect on the speciation of elements in water. 相似文献
11.
Detailed vertical profiles were taken in the north basin of lake Windermere between July and November 1980. Measurements were made of temperature, dissolved oxygen, pH, total suspended load and the major-element composition (organic C, Al, Fe, Mn, Si, S, P, Ca, Mg, Ba and K) of suspended particles.Excess concentrations (those reactive phases not supported by detrital phases) of particulate S, P, Ca, Mg, Ba and K are highest in the epilimnion due to their incorporation into the growing phytoplankton. These elements are associated with planktonic organic matter and are rapidly recycled in the upper 25 m of this 60 m oxic lake. This is documented by the decrease with depth of both excess concentrations of S, P, Ca, Mg, Ba and K and their ratios to POC. Large concentrations of excess particulate Si occur in the hypolimnion as the result of the settling out of diatom skeletal matter produced near the surface during the spring bloom. These siliceous particles do not contain significant quantities of excess particulate S, P, Ca, Mg, Ba and K. This observation supports the conclusion that organic matter is the important recycling matrix for these inorganic elements.Elevated concentrations of excess particulate Mn at depth indicate that there is a Mn-redox cycle operating in the lake. 相似文献
12.
Influence of parent sediments on the concentration of heavy metals in urban and suburban soils in Turku,Finland 总被引：1，自引：0，他引：1
The purpose of this study was to examine the influence of parent sediment material on soil geochemistry and to locate possible pollution sources in the area of Turku town in southwestern Finland. The study area is glaciated terrain and subsurface samples were chosen to represent five different parent sediment materials: glacial till, glaciofluvial or littoral sand, clay, peat and marine mud. Elemental concentrations of surface (100 samples) and background soil (50 samples) were analysed by ICP-AES (Al, Ba, Ca, Co, Cr, Cu, Fe, K, Mg, Mn, Na, Ni, P, S, Sr, Ti, V) and by graphite furnace AAS (As, Cd, Mo, Se). Loss-on-ignition was determined as an indicator of organic matter. Analytical results were examined using multivariate statistical methods. The results indicate that the studied soils are not heavily contaminated; there were only few sample sites with elevated heavy metal concentrations. High Pb concentrations were observed along main traffic routes, and also in places where there has been small-scale use of antifouling paints. However, concentrations of heavy metals in topsoil were in general significantly lower than those measured in large cities elsewhere. The parent material strongly affects the geochemical character of the soils. Clays naturally have a significantly higher concentration of heavy metals than sands or till material. This is also reflected in concentrations in organic topsoil. When assessing target levels for polluted soil, the primary sediment appears to be a more important factor than the amount of organic matter. 相似文献
13.
《Applied Geochemistry》2001,16(3):387-396
The concentration variations of 16 trace elements were determined along the main stem of a medium-sized stream (catchment area=107 km2), which drains areas covered with acid sulphate soils developed on sulphide-bearing marine sediments. During high flows in autumn, there was a strong downstream increase in the concentrations of Al, Cd, Co, Cu, Mn, Ni, Se, U and Zn and a moderate increase in those of Cr and Tl, related to extensive leaching of the acid sulphate soils, which increase in abundance from the headwater towards the basin outlet. During high flow in early summer, the downstream increase in the concentrations of these elements was not as strong as in autumn, due to decreased amounts of available mobile element fractions in the acid sulphate soils. Under baseflow conditions, the runoff from areas with acid sulphate soils is low in comparison to that in areas covered with other soils/sediments, resulting in relatively small loads of trace elements throughout the stream. The concentration variations of As, Pb, Sb, Ti and V were unrelated to catchment cover and did not vary along the stream in a regular manner. These 5 elements are, therefore, in contrast to the others, not leached more abundantly from the acid sulphate soils than from other soils/sediments. Based on the identified hydrogeochemical features and controls, it is suggested that water-quality improvement measures should include methods that primarily aim at reducing the leaching of hazardous chemical elements in the source areas (acid sulphate soils). 相似文献
14.
Over the last few years there has been growing concern over the mobilisation of anthropogenically derived, atmospherically deposited Pb from upland blanket peat soils to receiving surface waters. The near-surface layer of blanket peat soils of the Peak District, southern Pennines, UK, is severely contaminated with high concentrations of Pb. Erosion of peat soils in this upland area may be releasing large quantities of previously deposited Pb into the fluvial system. Samples of fluvial sediments (suspended, floodplain, streamside fan, trash-line and channel bed) were collected from a severely eroding blanket peat catchment in the Peak District in order to investigate Pb contamination of fluvial sediments, to determine the mechanism for fluvial Pb transport and to determine if erosion of contaminated peat soils in the catchment is releasing Pb into the fluvial system. Concentrations of Pb associated with fluvial sediments are considerably higher than those in the catchment geology, but not as high as those in peat soils in the catchment. Intra- and inter-storm variability in the Pb content of suspended sediments can be explained by differences in organic matter content of these sediments and differences in erosion processes operating within the catchment. High Pb concentrations are associated with suspended sediments that have a high organic matter content. The results of this study suggest that organic matter is the principle vector for sediment-associated Pb in the fluvial system. Erosion of contaminated peat soils in the Peak District is releasing Pb into the fluvial system. The extent to which this is a problem in other peatland environments is an area requiring further research. 相似文献
15.
Thirty four elements dissolved in water and 33 elements bound in particulate matter were analysed in the small river Saale (Thuringia, Germany, MQ=23 m3/s) in 1996 and the results were compared with those obtained in 1950 (44 elements). Monthly sampling was used to eliminate fluctuations caused by seasons and weather. Comparison of the element contents of a river over a 40-year-time span provides interesting insight into the anthropogenic change in the catchment area of the river with regard to „global change”.Without taking into consideration systematic errors, the analysed elements can be divided into three groups:
- (a) Elements whose average annual analytical values in 1996 were lower by >50% than those in 1950: Al, As, Ba, Fe, Pb, Zn (in solution), and As, B, Cr, Li, Mn, Pb, Se, Sn, U (suspended).
- (b) Elements whose average annual analytical values in 1996 are in the range of those in 1950, i.e., are within 50–150%: Ca, Co, Cr, F, K, Li, Mn, Na, Si, Sr, Ti, U (in solution), and Hg, Cr, Cu, Sc, Sr, Ti, Zn (suspended).
- (c) Elements whose average annual analytical values in 1996 were higher by >150% than those in 1950: B, Cd, Mg, Ni, Rb, Sc (in solution), and Ba, Ni, P, Zr (suspended).
16.
The chemistry of suspended matter in Esthwaite Water,a biologically productive lake with seasonally anoxic hypolimnion 总被引：1，自引：0，他引：1
Ten detailed vertical water column profiles were taken between April and November, 1979, in Esthwaite Water (English Lake district), a lake with high biological productivity and a seasonally anoxic hypolimnion. Measurements of the major-element particle composition (organic C, P, S, Si, Al, Ti, K, Mg, Ca, Fe, Mn, and Ba) and hydrochemical constituents (temperature, pH, dissolved oxygen, total suspended load, dissolved Fe, Mn, P, and Ba) were carried out. These have revealed new information about the mechanisms and kinetics of biogeochemical cycles in a lake.Pronounced seasonal cycles exist in which large excess concentrations (those unsupported by detrital components) of particulate organic C, Fe, Mn, P, S, Mg, K, Ba, and Ca are being generated and lost in situ in the water column (15m deep). In the epilimnion these elements (excepting Fe and Mn) are incorporated into the organic components of growing phytoplankton during the spring and summer. Simultaneously, in the hypolimnion there is a build-up and then a decrease in the excess concentrations of particulate C, P, S, Mg, K, Ba and Ca; this cycle is due to the indirect involvement of these elements with the iron redox cycle. As the hypolimnion becomes anoxic, dissolved ferrous Fe is released from the sediments and large concentrations of excess particulate iron (III) oxides accumulate; these oxides act as adsorbing substrates for the above mentioned elements. As conditions become more reducing, these same elements are solubilized as the iron (III) oxide particles are reduced to dissolved ferrous iron.Adsorption equations are derived from the field data which relate the concentration of excess particulate Fe to those of POC, P, S, Ca, Mg, Ba, and K. At the last stages of anoxia (before the lake overturns) large populations of bacteria and the formation of iron sulfide particles control the concentrations of excess particulate C, S, P, Mg, K, and Ca. 相似文献
17.
Two hundred and forty water samples (in four seasons) and seventeen sediment samples have been analyzed to monitor the natural and anthropogenic influences on the water and sediment chemistry of the Dal Lake, Kashmir Himalaya. The scatter diagrams [(Ca+Mg)/total cations (TZ+), (Ca+Mg)/HCO3, (Ca+Mg)/(HCO3+SO4), (Na+K)/TZ+; (Ca+Mg)/(Na+K)] and the geological map of the study area suggest predominance of carbonate and silicate weathering. Lower pH and high total dissolved solids, electrical conductivity and
values in the Gagribal basin and in some patches of other basins reflect anthropogenic inputs in the form of sewage from surrounding population, houseboats, hotels, etc. The Dal Lake is characterized by high chemical index of alteration (CIA: 87–95), reflecting extreme weathering of the catchment area. Relative to the average carbonates, the lakebed sediments are enriched in Al, Ti, Zn, Cu and Co and depleted in Ni and Mn. Compared to the post-Archean Shale the sediments have higher Al, Zn and Cu contents and lower Ni and Co. There are distinct positive anomalies of Al, Mn, Zn and Cu and negative anomalies of Ni and Pb with respect to the upper continental crust. Geoaccumulation index (I
geo) and the US Environmental Protection Agency sediment quality standards indicate that the Gagribal basin and some patches of the Nagin basin are polluted with respect to Zn, Cu and Pb. These data suggest that the Dal Lake is characterized by differential natural and anthropogenic influences. 相似文献
18.
In support of IGCP Project 259 (International Geochemical Mapping), a pilot survey designed to test the effectiveness of analysing dried humus collected at an extremely low sampling density (one composite sample per 23 000 km2) for geochemical mapping was carried out in 49 large catchment basins in Fennoscandia. The samples were analysed for their aqua-regia leachable contents of 30 elements by ICP-ES. The results were compared with those of till sampled at the same sites and with moss from previous surveys. The correlation with underlying bedrock was also studied.Geological features exert only a weak influence on the regional distribution of elements in humus. Exceptions are high levels of Ca and Sr in areas of carbonate bedrock and low contents of K in areas of Archean rocks. The distribution patterns of Co, Cr, Cu, Mg, Ni and Zn in humus coincide partly, and the levels correlate positively with those in till. The contents of Ni, Cr and Cu are lower in humus overlying acid magmatic rocks and arkose than other rock types.Pollution is the obvious source of high concentrations of Pb, Cd and Zn in southern Sweden and southern Norway. Acid fallout seems to cause leaching of Al, P and La from the humus horizon. The contents of these elements are low in the south where deposition of S and N is high and pH of rainwater is below 4.5. Deposition of sea salts gives high levels of Na, Mg, K and B along the coast of Norway and southern Sweden.The contents of several elements in humus correlate positively with the amount of organic matter (LOI). Comparison between four types of forest shows that the contents of Ca, Mg and Na in birch forest and of Cd, Mn, Pb and Zn in spruce forest are significantly higher than in other forest types. These features, however, are considered false and are due to sources such as atmospheric deposition of anthropogenic metals and sea salt.The results of the relatively strong chemical attack used for analyses of humus samples are less informative than those from till and overbank sediments. A weaker attack may have given more useful information. The humus horizon could be suited for environmental monitoring if used in global geochemical mapping. 相似文献
19.
通过对秦岭南坡中山地带火地塘林区大气降水与支沟溪流水和流域出口径流水质的比较分析,以及溪流水和流域出口径流水质与水量的相关分析,发现7~10月份大气降水呈微酸性,经过森林生态系统的调节,径流pH值升高,且不随流量变化而发生变化;森林生态系统对随降水输入的NO3-、NH4+、PO43-有很好的净化作用,这种作用对于降低南水北调中线工程取水地丹江口水库水质富营养化的威胁非常有益,对重金属元素Cd、Pb、Mn有固定作用;对K、Na、Ca、Mg、Fe有增加作用,尤其对Ca、Mg含量增幅较大,但这种作用不会对水质产生不良影响,对Fe的调升有利于水质改善;森林生态系统在调减Zn含量方面作用显著;林区径流水质与水量之间并无较大关系,水质不随水量变化而发生较大变化,森林生态系统对水质有很好的稳定作用。 相似文献
20.
Yves Goddéris Louis M. François Jacques Schott David Labat 《Geochimica et cosmochimica acta》2006,70(5):1128-1147
A numerical model of chemical weathering in soil horizons and underlying bedrock (WITCH) has been coupled to a numerical model of water and carbon cycles in forest ecosystems (ASPECTS) to simulate the concentration of major species within the soil horizons and the stream of the Strengbach granitic watershed, located in the Vosges Mountains (France). For the first time, simulations of solute concentrations in soil layers and in the catchment river have been performed on a seasonal basis. The model is able to reproduce the concentrations of most major species within the soil horizons, as well as catching the first-order seasonal fluctuations of aqueous calcium, magnesium and silica concentrations. However, the WITCH model underestimates concentrations of Mg2+ and silica at the spring of the catchment stream, and significantly underestimates Ca2+ concentration. The deficit in calculated calcium can be compensated for by dissolution of trace apatite disseminated in the bedrock. However, the resulting increased Ca2+ release yields important smectite precipitation in the deepest model layer (in contact with the bedrock) and subsequent removal of large amount of silica and magnesium from solution. In contrast, the model accurately accounts for the concentrations of major species (Ca, Mg and silica) measured in the catchment stream when precipitation of clay minerals is not allowed. The model underestimation of Mg2+ and H4SiO4 concentrations when precipitation of well crystallized smectites is allowed strongly suggests that precipitation of well crystallized clay minerals is overestimated and that more soluble poorly crystallized and amorphous materials may be forming. In agreement with observations on other watersheds draining granitic rocks, this study indicates that highly soluble trace calcic phases control the aqueous calcium budget in the Strengbach watershed. 相似文献