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1.
The pH, electrical conductance and concentration of six anions and 33 cations were determined in stream waters sampled in 1994 from eight arctic catchments on and adjacent to the Kola Peninsula (Russia, Finland and Norway). The catchments are located at various distances (5–300 km) from the major industrial emissions centres of Monchegorsk, Nikel and Zapoljarniy in Russia. The source of the elements can be (1) natural, marine (sea spray), (2) natural, geogenic (blowing soil/dust, till, bedrock), and/or (3) anthropogenic, industrial (emissions from smelters, dust from mining, etc.), each source showing a distinct signature. The median concentration of many contaminants can vary by up to three orders of magnitude from polluted to remote locations, and the concentration ranges observed in different catchments often do not overlap. This implies that contamination falls sharply with distance from source, but is quite profound and lasting close to the emission centres. Elevated trace metal contents in the most polluted streams indicates that deposited contaminants are transferred to the aquatic ecosystem, and eventually can reach the ocean.  相似文献   

2.
Stream water composition, measured weekly for 8–9 months in 1994 in three arctic catchments on and around the Kola Peninsula (Russia, Finland and Norway), is presented in the form of time-series. In all three catchments, snowmelt causes a major dilution of the stream water, as reflected by marked dips in electrical conductance. In the most polluted catchment (C2), the snowmelt flood (the major hydrological event at these latitudes) is reflected in the stream water by a pH dip and a pulse in technogenic heavy metals (Cu, Ni, etc.), Al and S. This results from melting of the snow laden with heavy metals and sulphate, and from leaching of the topsoil layer. In the most pristine catchment (C8), snowmelt causes no heavy metal pulse (remote location) but yields an increase in stream water Al (acidic lithology/overburden). In the intermediate catchment (C5), very subdued heavy metal and S increases are noticeable in the stream water, whilst its pH increases steadily until summer (basic lithology). Some elements (Cl, S) may be mobilised out of the snowpack before its complete thawing and reach the stream 1–2 weeks ahead of the heavy metals. The substrate (soil, overburden and bedrock) of a catchment controls to a large extent its ability to buffer acid inputs.  相似文献   

3.
Samples of topsoil together with reference samples of subsurface soil from a depth of 80–90 cm were collected in the central-northern part of the Zambian Copperbelt to distinguish lithogenic sources of metals from anthropogenic contamination of soils caused by fallout of dust from mining operations, flotation ore treatment plants, tailings dams, smelters and slag dumping grounds. The total sulphur, Cu and Co contents were found to be significantly higher in topsoil relative to subsurface soil over a large part of the surveyed area, and Zn, Pb, As and Hg contents showed a definite increase in the close neighbourhood of smelters and in the direction of prevailing winds. This indicates that the increase of these elements in the topsoil is due to anthropogenic activities. The areal extent and degree of anthropogenic contamination of topsoil can be expressed by an enrichment index (EI) based on the average ratio of the actual and median concentrations of the given contaminants. Although the contamination of soil by dust fallout decreases progressively with depth in the soil profile, in areas strongly affected by mining and mineral processing the anthropogenic contamination by sulphur and copper can be traced to a depth of 80–90 cm. In contrast, the concentration of elements such as Cr, Ni, and V, that show a direct correlation with the content of iron in the soils, increases in the subsurface soil relative to the topsoil. This is particularly evident in areas underlain by rocks of the Katanga Supergroup.  相似文献   

4.
A genetic relationship is shown for the noble-metal mineralization (up to 11.3 g/t of Pt and platinoids and 2.58 g/t of Au) discovered in the Poperechnoe Fe–Mn deposit and the fluid–explosive breccias. The composition of platinoid minerals is in agreement with the characteristics of ore and placer formations of the Ural–Alaskan type and corresponds to the isoferroplatinum–osmium igneous paragenesis. The noble metals were crystallized at the conditions that should take place at the crust–mantle boundary under partial melting of the slab rocks. The near-surface occurrence of these metals is caused by the rising of high-mobile fluid flows. The data obtained testify to the expedience of searches for noble metals associated with occurrences of fluidolites.  相似文献   

5.
The geology of the Volkovsky deposit, the composition of its rocks, titanomagnetite and copper-titanomagnetite ores with accompanying noble-metal mineralization, and their formation conditions are considered. Special attention is paid to the recently revealed noble-metal mineralization and its attendant character in respect to titanomagnetite ore is shown. Ore minerals and their relationships are characterized. Initially immiscible sulfide segregations are described and their evolution is traced up to interrelations with oxide and silicate cumulates. The distribution of noble metals (NM) in titanomagnetite and copper-titanomagnetite ores is discussed. Throughout ore formation, NM gradually accumulated in silicates, oxides, and sulfides. The highest NM concentrations are related to the sulfide schlieren and veinlike segregations in gabbroic rocks. It is suggested that the deposit was formed as a product of fractionation of basaltic magma. The copper-iron ore was deposited from the residual melt enriched in Cu, Fe, Ti, V and volatile P and S in a wide temperature range of 800 to 570°C. Noble metals concentrated in parallel with their own minerals (largely tellurides and native gold) at the final stage of crystallization of gabbroic intrusion.  相似文献   

6.
The abandoned Hg mine in Podljubelj was in operation with interceptions from 1557 to 1902. The entire operating period yielded about 110 000 tons of ore, from which 360 tons of Hg was produced. The objective of the research project was to establish the contents and spatial distribution of Hg in soils and stream sediments in the vicinity of the mine. On an area of 88 ha the soil was sampled in a 100 × 100 m grid. Two soil horizons (0–5 cm and 20–30 cm) were sampled in order to distinguish between geogenic and anthropogenic Hg sources. It was established that on an area of about 9 ha Hg content in soil exceeds The New Dutchlist action value for Hg (10 mg/kg). Total Hg concentrations in soil samples vary between 0.17 and 719 mg/kg, with a mean of 3.0 mg/kg. Mercury contents in stream sediments range from 0.065 to 1.4 mg/kg, with a mean of 0.64 mg/kg. The highest determined value in soils was found in the area around the former roasting furnace, where the ore was processed. Increased Hg concentrations were also found on the mine waste dump (108 mg/kg). Mercury contents in soils generally decrease with soil profile depth and with the distance from the mine and from the roasting furnace location. Mercury also appears in higher concentrations along the road that runs through the valley, which results from the use of Hg-bearing ore residues in road construction. The average enrichment factor (EF) of Hg in topsoil with respect to subsoil is 3.3. Calculated enrichment factors show higher values also for Cd (3.2), Pb (2.7), Ca (2.4) and P (1.9). The average enrichment factor of Hg in topsoil with regard to the established Slovenian soil averages (EFslo) is 19. EFslo of other determined chemical elements do not exceed 3.0.  相似文献   

7.
The Cr and Ni contents are high in the Eocene lignite of the Shenbei coalfield, which is a small intracontinental basin located in Liaoning Province, China. In this paper, we studied the distribution, origin and occurrence of Cr, Ni and other hazardous trace elements in the Shenbei lignite on the basis of coal petrology, and geochemistry of the lignite and combustion products. The following conclusions on the Shenbei lignite can be drawn: (1) The dominant maceral group in the Shenbei coal is huminite (humodetrinite), accounting for 96%–99% of the total maceral. Inertinite content is less than 1%. Liptinite content (sporinite and cutinite) is 0.2–1.6%. Common minerals in the Shenbei lignite include clay minerals (kaolinite), pyrite and quartz, and calcite and siderite. Chromite is not present in the lignite. (2) Potentially hazardous trace elements such as Co (22 μg/g), Cr (79 μg/g), Cu (63 μg/g), Zn (93 μg/g), V (88 μg/g) and Ni (75 μg/g) are strongly enriched in the Shenbei lignite compared with average concentration of trace elements in the Chinese coal and worldwide lignite. These elements are mainly associated with fulvic acid (FA) and/or coal organic macromolecular compounds in most of the studied lignite samples, indicating an organic association and enrichment of these elements in the Shenbei lignite. (3) Unusually high trace elements contents in the Shenbei lignite are derived mainly from the olivine basalt (country rock of coal basin) that consists of 52.7% plagioclase, 17.8% pyroxene, 14% olivine and 15.5% Ti–Fe oxide minerals. These olivine basalts have higher Cr, Ni, Pb and Zn contents than other types of rock and worldwide basalts do. (4) Fly ash of the Shenbei lignite, with 90% 1–50 μm amorphous particles and 8% 1–10 μm cenosphere, has high contents of Zn (23,707 μg/g), Be (12 μg/g), Sr (1574 μg/g), Pb (486 μg/g) and Cr (349 μg/g). In particular, the ferruginous micro-cenoshperes contain 1–12.79% Zn. Fine bottom ash (<0.031mm) of the Shenbei lignite has higher contents for most of the elements with the exception of Mo, Sn and Zn. Therefore, the potentially environmental and health impact of the fly ash and fine bottom ash should constitute a major concern.  相似文献   

8.
Sixty-five sediment samples and 25 water samples were collected from Al-Mujib reservoir, central Jordan, in order to investigate the heavy metal and ionic contamination assessment. Therefore, to achieve this aim, water and sediment samples were collected during winter and summer seasons (2007) from Al-Mujib reservoir and the areas surrounding it. The study shows that there are elevated levels of SO4 2−, Cl− and Na+ in reservoir water, which might originate from anthropogenic activities in the reservoir catchment area. In addition, the reservoir water has higher total hardness (TH) values together with high Ca and Mg contents. This might be attributed to pH of reservoir water and the nature of the rocks exposed in the catchment area. The average levels of heavy metals in reservoir sediments are Fe = 14,888.1, Cu = 17.8, Zn = 88.6, Ni = 38.7, Cd = 4.4, Mn = 337.9 and Pb = 6.1 mg/kg, which are lower than that observed in Wadi Al-Arab reservoir, northern Jordan. The values of enrichment factor are Cd = 35.5, Ni = 3.02, Zn = 2.54, Cu = 1.26, Mn = 1.2 and Pb = 0.57; these values indicate that heavy metals in sediments of Al-Mujeb reservoir have a different anthropogenic incrimination inputs. The study showed that the sediments are polluted with Cd, relatively contaminated with Ni and Zn and uncontaminated with respect to Mn, Pb and Cu.  相似文献   

9.
Gold has been exploited intensively in the Brazilian Amazon during the past fifteen years using garimpo methods (small-scale gold mining). In this study, two gold mining areas were investigated, the municipalities of Pocone and Alta Floresta located in the state of Mato Grosso. Central Brazil. The elemental mercury (Hg) used in amalgamating the gold, the final stage of the ore dressing process, has caused abnormal Hg concentrations in waterways. This has occurred principally in the Amazon region, where most of the ore prospected is alluvial. Background levels of metals were determined by analyzing sediments and soils located upstream of the anthropogenic inputs and unaffected by mining activities. The study aimed to evaluate the pollution level in sediments and soils, taking into account drainage waters directly affected by gold mining. ‘Geoaccumulation indexes’ (Igeo) of Hg in sediments from both study areas were used to assesses the pollution level in the aquatic environment. The geoaccumulation indexes of Hg in sediments of the Bento Gomes River in Pocone indicate a relatively high degree of pollution at some sites, even reaching class 4 (1.85 mg/kg). However, when the river reaches the Pantanal swamp, Hg concentrations drop considerably to 0.30 mg/kg. This drop seems to be due to accumulation of metals in the sediments of a lake (sampling site PG-24), which retains most of the sediments transported by the Bento Gomes River. Accumulation of metals in the lake also occurred for Cu, Pb, Zn, Fe and Mn. In the region of Alta Floresta, total Hg concentrations in sediments of the Teles Pires River were studied in the grain size fractions < 74 μm and > 74 μm. Hg concentrations in bottom sediments of this river were higher than those found in the Pocone region, with increases of 1.5 to 30 times the background, and thus reaching an Igeo up to class 5.  相似文献   

10.
《Applied Geochemistry》2003,18(2):283-309
International agreements (e.g. OSPAR) on the release of hazardous substances into the marine environment and environmental assessments of shelf seas require that concentrations and bioavailability of metals from anthropogenic sources can be distinguished from those originating as a result of natural geological processes. The development of a methodology for distinguishing between anthropogenic and natural sources of metals entering the Irish Sea through river inputs is described. The geochemistry of stream, river and estuarine sediments has been used to identify background geochemical signatures, related to geology, and modifications to these signatures by anthropogenic activities. The British Geological Survey (BGS) geochemical database, based on stream sediments from 1 to 2 km2 catchments, was used to derive the background signatures. Where mining activity was present, the impact on the signature was estimated by comparison with the geochemistry of sediments from a geologically similar, but mining free, area. River sediment samples taken upstream and downstream of major towns were used respectively to test the validity of using stream sediments to estimate the chemistry of the major river sediment and to provide an indication of the anthropogenic impact related to urban and industrial development. The geochemistry of estuarine sediments from surface samples and cores was then compared with river and offshore sediment chemistry to assess the importance of riverine inputs to the Irish Sea. Studies were undertaken in the Solway, Ribble, Wyre and Mersey estuaries. The results verify that catchment averages of stream sediments and major river samples have comparable chemistry where anthropogenic influences are small. Major urban and industrial (including mining) development causes easily recognised departures from the natural multi-element geochemical signature in river sediment samples downstream of the development and enhanced metal levels are observed in sediments from estuaries with industrial catchments. Stream sediment chemistry coupled with limited river and estuarine sampling provides a cost-effective means of identifying anthropogenic metal inputs to the marine environment. Investigations of field and laboratory protocols to characterise biological impact (bioaccumulation) of metals in sediments of the Irish Sea and its estuaries show that useful assessments can be made by a combination of surveys with bioindicator species such as clams Scrobicularia plana, selective sediment measurements that mimic the ‘biologically available’ fractions, and laboratory (mesocosm) studies.  相似文献   

11.
Summary Fifteen snow samples were collected at the end of the 1995/96 winter in the vicinity (1.5–8 km) of the copper-nickel processing plants at Zapoljarnij, Nikel and Monchegorsk on the Kola Peninsula, NW Russia. Polished sections were made from the snow filter residues for microscopic and qualitative and quantitative electron microprobe investigations. Particles in snow are derived from either geogenic1, or technogenic sources2. Ore particles from two different Ni-Cu deposits can be identified in the snow: i) local Pechenga ore and ii) imported ore from Norilsk-Talnakh. Technogenic particles consist of a wide spectrum of sulphides (Ni-Cu-Fe-Co), oxides (Fe-Ni-Cu), metallic phases and alloys (Ni-Cu-Fe-Co), as well as slag particles and coke. Differences in the processing technologies used in the three plants (e.g. roasting, smelting to Cu-Ni matte, converting, refining) can be deduced from the mineralogy of the particulate emissions. The mineralogy of particulate matter in snow is characteristic for each emitter and can thus be used to fingerprint different sources. PGE-bearing sulphides (pentlandite with 0.2–0.3 wt% Pd) have been observed in the particulate emissions from Zapoljarnij and discrete PGE-phases at Monchegorsk.
Mineralogie und Mineralchemie von Schnee-Filtraten aus dem Bereich der NickelKupfer Kombinate der Kola-Halbinsel, NW Rußland
Zusammenfassung Fünfzehn Schneeproben wurden in der Nähe (1.5–8 km) von Kupfer-Nickel-Minen und Mitten in Zapoljarnij, Nikel und Monchegorsk auf der Halbinsel Kola, NW Rußland, am Ende des Winters 1995/96 genommen. Anschliffe von Schneefilterrückständen wurden für die mikroskopischen Untersuchungen Bowie für qualitative und quantitative Mikrosondenanalytik angefertigt. Die in den Anschliffen beobachteten Phasen sind teils geogener1, teils technogener2 Herkunft. Die geogenen Partikel sind Teil der lokalen Staubemissionen (Pechenga Ni-Cu-Tagebaue, Transport und Aufbereitung von Erzen). Die technogenen Partikel repräsentieren ein breites Spektrum unterschiedlich zusammengesetzter Sulphide (Ni-Cu-Fe-Co), Oxyde (Fe-Ni-Cu), metallischer Phasen und Legierungen (Ni-Cu-Fe-Co), sowie Schlacke-Partikel und Koks. Variationen der Zusammensetzung und im Auftreten dieser Phasen ermöglichen Rückschlüsse auf die im Prozess eingesetzten Erze und auf verschiedene Stadien der Prozesstechnik (z.B. Rösten, Schmelzen auf Cu-Ni Stein, Konvertieren auf Cu-Ni Feinstein, Raffinieren) in den lokalen Haupternittenten. Ausserdem konnten PGE-führende Sulphide (Pentlandit mit 0.2–0.3 Gew% Pd) und separate PGE-Phasen in den partikulären Emissionen von Zapoljarnij and Monchegorsk identifiziert werden.

With 8 Figures  相似文献   

12.
Due to rapid industrialization, urbanization and intensive agriculture in India increasing contamination of heavy metals in soil has become a major concern. An environmental geochemical investigation was carried out in and around the Pali industrial development area of Rajasthan to determine the effect of contamination in the study area. Soil samples collected near the Pali industrial area were analyzed for Pb, Cr, Cu, Zn, Sr and V contents by using Philips PW 2440 X-ray fluorescence spectrometer. Samples were collected from the industrial area of Pali from the top 10 cm layer of the soil. Most of the samples were collected near small streams adjacent to industrial areas, and near Bandi River. Levels of the metals in soils around the industrial area were found to be significantly higher than their normal distribution in soil such as Pb – 293 mg/kg, Cr – 240 mg/kg, Cu – 298 mg/kg, Zn – 1,364 mg/kg, Sr – 2,694 mg/kg and V – 377 mg/kg. High concentration of these toxic elements in soil is responsible for the development of toxicity in agriculture products, which in turn affects human life. Distribution of metals, their contents at different locations, correlation of heavy metals in soil and their effect on human health are discussed in the paper.  相似文献   

13.
New data are presented on the contents of Fe, Mn, Zn, Cu, Pb, Cd, and Ni in dissolved and particulate modes of occurrence in unpolluted or anthropogenically contaminated major rivers of Primorye. The background contents of dissolved metals are as follows: 0.1–0.5 μg/l for Zn and Ni, 0.3–0.7 μg/l for Cu, 0.01–0.04 μg/l for Pb and Cd, and 2–20 μg/l for Fe and Mn. Common anthropogenic loading (communal wastewaters) notably increases the dissolved Fe and Mn concentrations Industrial wastes lead to a local increase in the contents of dissolved metals in river waters by one to three orders of magnitude. The effect of hydrological regime is expressed most clearly in the areas of anthropogenic impact. The metal contents in the particulate matter are controlled mainly by its granulometric composition. Original Russian Text ? V.M. Shulkin, N.N. Bogdanov, V.I. Kiselev, 2007, published in Geokhimiya, 2007, No. 1, pp. 79–88.  相似文献   

14.
This paper describes the influence of siliceous and iron-rich calcic low-temperature hydrothermal fluids (LTHF) on the mineralogy and geochemistry of the Late Permian No. 11 Coal (anthracitic, Rr=2.85%) in the Dafang Coalfield in northwestern Guizhou Province, China. The No. 11 Coal has high contents of vein ankerite (10.2 vol.%) and vein quartz (11.4 vol.%), with formation temperatures of 85 and 180 °C, respectively, indicating that vein ankerite and vein quartz were derived from low-temperature calcic and siliceous hydrothermal fluids in two epigenetic episodes. The vein quartz appears to have formed earlier than vein ankerite did, and at least three distinct stages of ankerite formation with different Ca/Sr and Fe/Mn ratios were observed.The two types of mineral veins are sources of different suites of major and trace metals. Scanning electron microscope and sequential extraction studies show that, in addition to Fe, Mg, and Ca, vein ankerite is the dominant source of Mn, Cu, Ni, Pb, and Zn in the coal, and the contents of these five elements are as high as 0.09% and 74.0, 33.6, 185, and 289 μg/g, respectively. In contrast, vein quartz is the main carrier mineral for platinum-group elements (PGEs) Pd, Pt, and Ir in the coal, and the contents of Pd, Pt, and Ir are 1.57, 0.15, and 0.007 μg/g, respectively. Sequential extraction showed a high PGE content in the silicate fraction, up to 10.4 μg/g Pd, 1.23 μg/g Pt, and 0.05 μg/g Ir, respectively. It is concluded that the formation of ankerite and quartz and the anomalous enrichment of trace elements in the No. 11 Coal in the Dafang Coalfield, Guizhou, result from the influx of calcic and siliceous low-temperature hydrothermal fluids.  相似文献   

15.
Identification of reliable background values of potentially toxic metals in sediments requires detailed integration of geochemical data with accurate sedimentological studies. Through analysis of 60 soil samples from the Pisa coastal plain, this study shows to what extent sediment provenance and facies characteristics may influence the natural distribution of potentially toxic metals (Cr, Ni, Cu, Zn, Pb) within alluvial and coastal sediments. Metals supplied to the alluvial plain are mostly concentrated within the finest sediment fraction (floodplain clays), while coarser crevasse and overbank deposits exhibit invariably lower metal contents. Beach-ridge sands display the lowest metal concentrations. Transport of ophiolitic detritus by the longshore drift may account for locally high Cr concentrations within beach deposits. Geochemical fingerprinting of individual facies associations in terms of natural metal contents results in the construction of a geologically-based geochemical map. This map offers a more reliable depiction of spatial distribution of background levels than interpolation techniques based uniquely upon statistical methods. Matching background values against metal concentrations from topsoil samples leads to the reliable assessment of the pollution status of Pisa coastal plain. Metal contents exceeding the threshold values designated for contaminated areas (Cr) simply reflect catchment geology, and are not the product of artificial contamination. On the other hand, anthropogenic disturbance may be detected even where metal contents (Pb, Cu) lie below the threshold values. The use of sedimentological criteria is presented here as a pragmatic tool to enhance predictability of natural metal contents in sediments, with obvious positive feedbacks for legislative purposes and environmental protection.  相似文献   

16.
This paper discusses the mineralogy and geochemistry of the No. 6 Coal (Pennsylvanian) in the Junger Coalfield, Ordos Basin, China. The results show that the vitrinite reflectance (0.58%) is lowest and the proportions of inertinite and liptinite (37.4% and 7.1%, respectively) in the No. 6 Coal of the Junger Coalfield are highest among all of the Late Paleozoic coals in the Ordos Basin. The No. 6 Coal may be divided vertically into four sections based on their mineral compositions and elemental concentrations. A high boehmite content (mean 6.1%) was identified in the No. 6 Coal. The minerals associated with the boehmite in the coal include goyazite, rutile, zircon, and Pb-bearing minerals (galena, clausthalite, and selenio-galena). The boehmite is derived from weathered and oxidized bauxite in the weathered crust of the underlying Benxi Formation (Pennsylvanian). A high Pb-bearing mineral content of samples ZG6-2 and ZG6-3 is likely of hydrothermal origin. The No. 6 coal is enriched in Ga (44.8 μg/g), Se (8.2 μg/g), Sr (423 μg/g), Zr (234 μg/g), REEs (193.3 μg/g), Hg (0.35 μg/g), Pb (35.7 μg/g), and Th (17.8 μg/g). Gallium and Th in the No. 6 Coal mainly occur in boehmite, and the Pb-bearing selenide and sulfide minerals contribute not only to Se and Pb contents in the coal, but also probably to Hg content. A high Zr content is attributed to the presence of zircon, and Sr is related to goyazite. The REEs in the coal are supplied from the sediment-source region, and the REEs leached from the adjacent partings by groundwater.  相似文献   

17.
We present data on the location, chemical composition, and contents of trace elements in thin ferromanganese crusts at two sites of the submarine Vityaz’ Ridge: Diana and Bussol’ test grounds. The crusts abound in inclusions of grains of nonferrous (Cu, Zn, Pb, Sn, Ni, W) and noble (Au, Ag, Pd, Pt) metals in the form of native elements, sulfides, sulfates, oxides, or intermetallic compounds. The crusts at the Diana test ground contain mainly grains of nonferrous-metal minerals, and those at the Bussol’ test ground, mainly noble-metal minerals. There are also sites with Ni-rich (up to 3.5%) manganese crust. A detailed study of the ore crusts from the Vityaz’ Ridge showed that they are probably at the initial stage of formation.  相似文献   

18.
The mobility and retention of heavy metals, arsenic and sulphur in podzols from eight areas located north of the Arctic Circle in Finland, Norway and Russia were determined by analyzing the < 2.0 mm fraction, using an ammonium acetate (pH 4.5) extraction in addition to a concentrated nitric acid digestion for the humus samples, and a hot aqua regia digestion for the mineral soil samples. Total C, H and N concentrations were determined in humus and mineral soil samples with a CHN analyser.Ni, Cu, Co and As were strongly enriched in the humus layer in the contaminated sites (Monchegorsk, Kurka, Zapoljarnij) when compared to their concentrations in the parent tills and in podzols from the background sites. In most study sites the illuvial layer showed a low capacity to retain the metals and As, the exception included a strongly eroded profile at Monchegorsk, where Ni was tightly fixed in the illuvial layer while Cu was mobile. In contrast to metals, airborne S was not accumulated in the humus layer, but was accumulated in the illuvial layer, more markedly at eroded sites than in places where the humus was covered as at Monchegorsk.  相似文献   

19.
The Nickel Plate deposit, in which gold occurs as <25 μm blebs associated with arsenopyrite in garnet-pyroxene skarns, is in the subalpine zone near the southern limit of the Thompson Plateau. During the last glaciation the Cordilleran ice sheet moved south-southwest across the deposit and deposited a stony basal till. A dispersion train with anomalous concentrations of gold in tills and soils now extends 2 km down ice from the deposit.Gold contents of samples of humus (LFH horizon) and the −212 μm fraction of mineral soils (A, B and C horizons) was determined by instrumental neutron activation and fire assay-atomic absorption, respectively. Selected samples were examined in detail to determine distribution of gold between different size and density fractions.Despite erratic variability, Au contents of the −212 μm fraction generally decrease from 200–400 ppb close to the mine site to <50 ppb at distal sites. At most sites there is also a twofold increase of gold values down the soil profile. Within samples concentrations of Au in the −420 + 212 μm, −212 + 106 μm, −106 + 53 μm and −53 μm fractions are usually roughly constant. However, because of its abundance, the −53 μm fraction contains more than 70% of the gold. Amenability of gold in this fraction to cyanidation suggests that it is largely free gold. For size fractions > 53 μm the contribution of the heavy mineral (SG > 3.3) fraction to total gold content increases with decreasing grain size.Distribution of gold between size and density fractions is consistent with its release from the bedrock or pre-glacial regolith by glacial abrasion. The bulk of the gold was incorporated into the fine fractions of the till at or close to the source. However, differences between down ice dilution ratios for gold in different heavy mineral size fractions suggest that comminution of host minerals continued to transfer gold to the finer size fractions during glacial transport.For exploration purposes, B and C horizon samples provide the best anomaly contrast. Estimates of the abundance of gold particles in different size fractions indicate that the nugget effect, which causes erratic gold values in the −212 μm fraction, can be avoided by analysis of 30 g of −53 μm material.  相似文献   

20.
The amount of Cu and Fe associated with humic acids was estimated in five sediment cores from a tropical coastal lagoon (Piratininga Lagoon, Rio de Janeiro, Brazil). Core samples were analysed for humic acid contents, total Fe and Cu content. Fe and Cu associated with humic acids were also measured. Results show amounts of humic acids ranging from 0.7 to 21.7% of the dry weight of sediment (average 4.6%, standard deviation 4.4%). Concentrations of Fe and Cu ranged from 0.3 to 6.0% (average 2.2%, S.D. 1.2%) and from <1.0 to 65.0 μg g−1 (average 28.6 μg g−1, S.D. 16.4 μg g−1), respectively. The results of strongly bound metals show that while humic acids are the main carrier for Cu, Fe does not seems to be significantly associated with this organic matter.  相似文献   

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