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1.
The Okchon black shale in Korea provides a typical example of natural geological materials enriched with potentially toxic elements. The Chung-Joo, Duk-Pyung, Geum-Kwan, I-Won, Bo-Eun and Chu-Bu areas are underlain by these black shales and slates of the Guryongsan Formation or the Changri Formation, which are parts of the Okchon Group in the central part of the southern Korean Peninsula. In order to investigate the enrichment levels and dispersion patterns of potentially toxic elements in the rock–soil–plant system, environmental geochemical surveys were undertaken in the above six study areas in the Okchon Zone. After appropriate preparation, rock and soil samples were analyzed for potentially toxic elements by instrumental neutron activation analysis (INAA) and inductively coupled plasma atomic emission spectrometry (ICP-AES), and plant samples by atomic absorption spectrometry (AAS). In particular, Ba, Cd, Mo, V and U in Okchon black shales are highly enriched, and their mean concentrations are significantly higher than those in black slates. These elements are geochemically associated, and might be enriched simultaneously. The highest mean concentrations of 42.0 μg g−1 As, 2100 μg g−1 Ba, 10.9 μg g−1 Cd, 213 μg g−1 Mo, 83 μg g−1 U, 938 μg g−1 V and 394 μg g−1 Zn are found in black shales from the Duk-Pyung area. Mean concentrations of As, Mo and U in soils overlying black shales occurring in the Duk-Pyung area (30 μg g−1 As, 24 μg g−1 Mo and 50 μg g−1 U) and Chu-Bu area (39 μg g−1 As, 15 μg g−1 Mo and 27 μg g−1 U) are higher than the permissible level. Enrichment index values of the six study areas decrease in the order of Duk-Pyung > Chu-Bu > Bo-Eun > Chung-Joo > Geum-Kwan = I-Won areas. Relationships between trace element concentrations in soils and plants are significantly correlated, and the biological absorption coefficients (BAC) in plants are in the order of Cd > Zn = Cu > Pb, which suggests that Cd is more bioavailable to plants than the other elements. Cadmium concentrations in plant species decrease in the order of chinese cabbage > red pepper > soybean = sesame > rice stalk > corn > rice grain. From the result of sequential extraction analysis of soils, relatively high proportions of Cu, Pb and Zn are present as residual fractions, and that of Cd as non-residual fractions. Cadmium occurs predominantly as exchangeable/water-acid soluble phase in soils, and this is in agreement with the findings of high Cd concentrations in plants.  相似文献   

2.
Plant species that accumulate high levels of metals in proportion to the metal content in the soil are of considerable interest in biogeochemical and biogeobotanical prospecting. This study was aimed at investigating copper and nickel accumulation in the plants Helichrysum candolleanum and Blepharis diversispina, to assess their potential use as mineral indicators in biogeochemical prospecting. Soils and plants were collected from copper–nickel mineralised areas in Botswana. Analyses of the soils and the respective plant parts (roots, stem, leaves and flowers) were carried out using ultrasonic slurry sampling electrothermal atomic absorption spectrometry (ETAAS), which allowed rapid determination of copper and nickel in small amounts of the samples.The metal concentration in the soil was in the range ≈ 40 μg/g–4% (w/w) for Cu and ≈ 60 μg/g–0.3% (w/w) for Ni. The concentration ranges of the elements in the plant parts were ≈ 6 μg/g–0.2% Cu and ≈ 3–210 μg/g Ni. At high soil metal content (greater than 2.5% (w/w) Cu and 0.1% (w/w) Ni), high levels of both nickel and copper were found in the shoots (leaves and flowers) of H. candolleanum. Concentrations as high as 0.2% (w/w) Cu were found in the leaves and flowers of H. candolleanum, indicating hyperaccumulation for this plant. For B. diversispina, the metal concentrations did not exceed 100 μg/g for any plant part, for both metals. Both plant species tolerate high concentrations of metals and should therefore be categorized as metallophytes. In order to evaluate metal translocation from the soil to the shoots, metal leaf transfer coefficients (ratio of metal concentration in the leaf to metal concentration in the soil) were calculated. Our data suggest that the two plant species have different metal uptake and transport mechanisms, which needs to be investigated further. The present work also suggests that H. candolleanum may be used as a copper/nickel indicator plant in biogeochemical or biogeobotanical prospecting.  相似文献   

3.
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   

4.
Eight catchments, an area of 15 to 35 km2, have been studied within an ecogeochemical mapping programme in the western Kola Peninsula and contiguous parts of Finland and Norway. Three catchments, one northeast of Zapolyarniy (1) and two, 5 and 25 km south of Monchegorsk (2 and 4) show high levels of deposition of heavy metals, especially nickel (Ni) and copper (Cu), related to the metallurgical industry in these cities. Twenty-five topsoil samples, from sites evenly distributed over catchment 2, have mean contents of Ni and Cu 1 to 2 orders of magnitude higher than both C-horizon samples from the same sites and topsoil samples from catchment 4, providing strong evidence for the anthropogenic origin of the heavy metals. The same samples show geometric mean total contents for the noble metals analysed of: 1.4 μg/kg rhodium (Rh), 49.6 μg/kg platinum (Pt), 187.6 μg/kg palladium (Pd) and 9.5 μg/kg gold (Au). The pattern of concentration of the noble metals mirrors that found in published averages for ore from the Talnakh mineralizations in the Noril'sk province, though 1–2 orders of magnitude lower. This also clearly shows that the noble-metal contents of the topsoil are anthropogenic, and suggests that they emanate from the plants in Monchegorsk at an early stage in treatment of the ore, probably as a minor component of Ni-Cu rich particles. The noble-metal geochemistry of the topsoil in the other catchments also reflects the nature of the ore being processed at the plants nearby.  相似文献   

5.
Concentrations of total and dissolved elements were determined in 35 water samples collected from rivers in Sardinia, a Mediterranean island in Italy. The overall composition did not change for waters sampled in both winter and summer (i.e., January at high-flow condition and June at low-flow condition), but the salinity and concentrations of the major ions increased in summer. Concentrations of elements such as Li, B, Mn, Rb, Sr, Mo, Ba and U were higher in summer with only small differences between total and dissolved (i.e., in the fraction <0.4 μm) concentrations. The fact that these elements are mostly dissolved during low flow periods appears to be related to the intensity of water–rock interaction processes that are enhanced when the contribution of rainwater to the rivers is low, that is during low-flow conditions. In contrast, the concentrations of Al and Fe were higher in winter during high flow with total concentrations significantly higher than dissolved concentrations, indicating that the total amount depends on the amount of suspended matter. In waters filtered through 0.015 μm pore-size filters, the concentrations of Al and Fe were much lower than in waters filtered through 0.4 μm pore-size filters, indicating that the dissolved fraction comprises very fine particles or colloids. Also, Co, Ni, Cu, Zn, Cd and Pb were generally higher in waters collected during the high-flow condition, with much lower concentrations in 0.015 μm pore-size filtered waters; this suggests aqueous transport via adsorption onto very fine particles. The rare earth elements (REE) and Th dissolved in the river waters display a wide range in concentrations (∑REE: 0.1–23 μg/L; Th: <0.005–0.58 μg/L). Higher REE and Th concentrations occurred at high flow. The positive correlation between ∑REE and Fe suggests that the REE are associated with very fine particles (>0.015 and <0.4 μm); the abundance of these particles in the river controls the partitioning of REE between solution and solid phases.Twenty percent of the water samples had dissolved Pb and total Hg concentrations that exceeded the Italian guidelines for drinking water (>10 μg/L Pb and >1 μg/L Hg). The highest concentrations of these heavy metals were observed at high-flow conditions and they were likely due to the weathering of mine wastes and to uncontrolled urban wastes discharged into the rivers.  相似文献   

6.
This work addresses the mercury exposure scenarios through fish consumption in the urban area of Alta Floresta, by comparing the different patterns of mercury exposure from fish ingestion for different population groups. This study was based on field surveys that could provide background information, such as the characteristics of Hg sources, characteristics of local and regional environment, Hg concentrations in different media, and the characterization of the local urban population. The urban area of Alta Floresta is one of the most important gold-trading centers in Amazonia, where approximately 1 ton of gold has been commercialized monthly. The general adult urban population is exposed to low-level mercury concentration via fish consumption with an average daily intake of 0.2 μg/kg (b.w.) and an estimated hazard quotient of 0.7. However, the fishermen families present an average daily intake of 2.2 μg/kg (b.w.) and a hazard quotient of 8.6. The children of fishermen families between 5 and 14 years old are the main risk group for Hg exposure via fish ingestion. Based on the uncertainty analysis, the Hg fish concentrations and the fish ingestion rate were found to be the main parameters affecting the variability of the model outputs.  相似文献   

7.
In order to study the first steps of incorporation of lipids in recent organic-rich sediments into free and bound fractions, we have selected the Santa Barbara Basin, off California. This basin with a maximum of 590 m water depth is characterized by high phytoplankton production in surface waters and a low oxygen content in bottom waters. Sediments show the following features: high sedimentation rate ≈ 4 mm/yr, no bioturbation, and development of a bacterial mat community at the surface with predominance of sulphur-oxidizing bacteria trapping particles, thus preventing re-distribution of sediment, which permit a unique observations of organic sedimentation on a new few years basis.A sediment core has been divided into 2 cm thick slices corresponding to a time resolution of ≈5 years, from 1835 up to 1987. Samples have been analyzed using a multi-parameter approach, such as for plankton species identification, carbon stable isotope ratios and, as reported here, for lipid organic tracers. Organic tracers have been analyzed in the sterol and fatty series for both free and bound compounds by gas chromatography and gas chromatography/mass spectrometry.The incorporation processes of sterols with depth appear different for free and bound compounds. Total free sterol concentrations show high values in surface sediments (≈ 100 μg/g dry sediment), rapidly decrease up to ≈ 10 cm depth and remain at a constant value of 30–40 μg/g. Total bound sterol concentrations show low values in surface sediment (13.6 μg/g), and vary irregularly with depth up to a value of 55 μg/g at 7.3 m, and then remain constant at 25–26 μg/g.Profiles of evolution with depth of free C27, C28 sterols show a regular decrease, whereas C29 sterols show an irregular decrease with anomalies at 7.3 cm (approximately age: 1977–1978) and at 14.1 cm (1962–1964). Profiles of bound compounds are rather different, very regular for C28 sterols, irregular with oscillations for C27 and C29 sterols at 7.3, 12.2 and 18.0 cm (1954–1956), suggesting a different mode of incorporation and probably different inputs for C27, C29 and C28 sterols.The study of the kinetics of degradation of sterols between surface (1987) and 10.5 cm (1968–1972) shows that C27 compounds are degraded at a slight higher rate (0.53 μg/μg of initial C27 concentration/ year) than are C28 and C29 compounds (0.047 μg/μg of initial concentration/year). An intermediate value is found for brassicasterol: 0.049 μg/μg/year.  相似文献   

8.
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   

9.
Arkosic sandstones and conglomerates of Tertiary age beneath the Challis Volcanics of Eocene age at Basin Creek, 10 km northeast of Stanley, Idaho, contain uranium-bearing vitrainized carbon fragments. The economic potential of these sandstones and conglomerates is currently being assessed. Springs abound at the contacts of rock units, and water from these springs supports abundant growths of bryophytes (mosses and liverworts). Water from 22 springs and associated bryophytes were sampled; two springs were found to contain apparently anomalous concentrations (normalized) of uranium — as much as 6.5 μg/L (ppb) in water and 1800 μg/g (ppm) in ash of mosses. Moss samples from both springs also contained anomalous concentrations of arsenic, and one contained highly anomalous amounts of beryllium. Water from a third spring contained slightly anomalous amounts of uranium, and two species of mosses at the spring contained anomalous uranium (400 and 700 μg/g) and high levels of both cadmium and lead. Water from a fourth spring was normal for uranium (0.18 μg/L), but the moss from the water contained a moderate uranium level and highly anomalous concentrations of lead, germanium, and thallium.These results suggest that, in the Basin Creek area, moss sampling at springs may give a more reliable indication of uranium occurrence than would water sampling. The reason for this may be the ability of mosses to concentrate uranium and its associated pathfinder elements and to integrate uranium fluctuations that occur in the spring water over any period of time.  相似文献   

10.
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   

11.
This paper describes the influence of volcanic ash on the concentrations and occurrences of associated elements in coal in the Zhijin Coalfield in western Guizhou Province, China. Our studies reveal that the No. 9 coal seam in the Zhijin Coalfield has very high content of Fe (4.34%), Cu (369.90 μg/g), U (49.6 μg/g), Mo (63.10 μg/g), Zn (33.97 μg/g), and Zr (841.80 μg/g). The studies have also found that elements, such as Fe and Cu, do not occur as sulfides in this coal seam, in sharp contrast to many other coal seams in China. The geochemical and mineralogical anomalies of the coal seam are attributed to synsedimentary volcanic ash. In addition to normal macerals and minerals in coal, a volcanic-influenced material (VIM) derived from volcanic ash, detrital material of terrigenous origin and organic matter was identified under polarized-light reflectance microscopy and scanning electron microscopy equipped with energy-dispersive X-ray (EDX) analyzer. The volcanic-influenced material is the main carrier of the above elements in this coal. Six types of the volcanic-influenced material (VIM-1, VIM-2, VIM-3, VIM-4, VIM-5, and VIM-6) are further distinguished on the basis of their structures and compositions. To the best of our knowledge, this is the first report that presents a detailed classification of coal components with a high content of volcanic ash.  相似文献   

12.
The potential for using groundwater helium surveys in exploration has been evaluated by conducting local and regional surveys in several mineralized and background areas in Australia. Dissolved helium contents decrease markedly upwards, particularly in the top 10–15m, due to degassing in attaining dynamic equilibrium with the atmosphere. Gradients of depth profiles are not uniform but because total concentration variations to 50m or more are commonly less than 10, whereas regional variations are 103–105, samples from the greatest constant depth possible below water-table are adequate for survey purposes. Helium concentrations in excess of the atmosphere equilibrium value of 0.044 μl He/l H2O were found to be associated with uranium mineralization at Honeymoon (6.9–44.4 μl/l), Manyingee (0.08–1.68 μl/l), Bennett Well (9.9–29.5 μ/l) and the Stuart Shelf—Roxby Downs (910–2495 μl/l), with a carbonatite at Mt. Weld (0.18–13.6 μl/l), and with kimberlites at Wandagee (0.2–3.25 μl/l). No anomaly was associated with the shallow calcrete uranium deposit at Yeelirrie. However, equivalent or higher concentrations were found in groundwaters from unmineralized areas around these deposits, e.g. up to 85 μl/l at Manyingee—Bennett Well, to 215 μl/l at Yeelirrie and to 1525 μl/l, Stuart Shelf—Mt. Gunson. Similarly, helium in waters from stock wells near Mt. Weld appears to indicate the presence of the carbonatite but in a survey of a geologically similar area near Malcolm, equivalent anomalies were not related to carbonatite.Although the uranium (and thorium) mineralization is a significant source, high helium concentrations can arise by accumulation in groundwaters with long residence times and by leakage from deep sources, particularly granitoid basement. The concentration reached is also a function of the porosity and configuration of the aquifer and the permeability of the aquiclude to helium. These factors are more important in determining dissolved helium concentrations than the uranium and thorium contents of the rocks. However, the effects are not readily quantifiable, particularly in exploration areas where geology and hydrology are relatively unknown, hence helium groundwater data can be difficult if not impossible to interpret.  相似文献   

13.
Boehmite-rich coal of Pennsylvanian age was discovered earlier at the Heidaigou Surface Mine, Jungar Coalfield, Inner Mongolia, China. This paper reports new results on 29 bench samples of the no. 6 coal from a drill core from the adjacent Haerwusu Surface Mine, and provides new insights into the origin of the minerals and elements present. The results show that the proportion of inertinite in the no. 6 coal is higher than in other Late Paleozoic coals in northern China. Based on mineral proportions (boehmite to kaolinite ratio) and major element concentrations in the coal benches of the drill core, the no. 6 coal may be divided into five sections (I to V). Major minerals in Sections I and V are kaolinite. Sections II and IV are mainly kaolinite with a trace of boehmite, and Section III is high in boehmite. The boehmite is derived from bauxite in the weathered surface (Benxi Formation) in the sediment-source region. The no. 6 coal is rich in Al2O3 (8.89%), TiO2 (0.47%), Li (116 μg/g), F (286 μg/g), Ga (18 μg/g), Se (6.1 μg/g), Sr (350 μg/g), Zr (268 μg/g), REEs (172 μg/g), Pb (30 μg/g), and Th (17 μg/g). The elements are classified into five associations by cluster analysis, i.e. Groups A, B, C, D, and E. Group A (ash–SiO2–Al2O3–Na2O–Li) and Group B (REE–Sc–In–Y–K2O–Rb–Zr–Hf–Cs–U–P2O5–Sr–Ba–Ge) are strongly correlated with ash yield and mainly have an inorganic affinity. The elements that are negatively or less strongly correlated with ash yield (with exceptions of Fe2O3, Be, V, and Ni) are grouped in the remaining three associations: Group C, Se–Pb–Hg–Th–TiO2–Bi–Nb–Ta–Cd–Sn; Group D, Co–Mo–Tl–Be–Ni–Sb–MgO–Re–Ga–W–Zn–V–Cr–F–Cu; and Group E, S–As–CaO–MnO–Fe2O3. Aluminum is mainly distributed in boehmite, followed by kaolinite. The high correlation coefficients of the Li–ash, Li–Al2O3, and Li–SiO2 pairs indicate that Li is related to the aluminosilicates in the coal. The boehmite-rich coal is high in gallium and F, which occur in boehmite and the organic matter. Selenium and Pb are mainly in epigenetic clausthalite fillings in fractures. The abundant rare earth elements in the coal benches were supplied from two sources: the bauxite on the weathered surface of the Benxi Formation and from adjacent partings by groundwater leaching during diagenesis. The light rare earth elements (LREEs) are more easily leached from the partings and incorporated into the organic matter than the heavy REEs, leading to a higher ratio of LREEs to HREEs in the coal benches than in the overlying partings.  相似文献   

14.
An orientation survey was conducted over the Quartz Mountain, Oregon, hot-spring type disseminated gold deposit to address three questions critical to successful exploration of the area: What is the relationship between bedrock geology and the trace-element content of trees and soils; do these relationships change seasonally; are these relationships similar in the two tree species which discontinuously blanket the area?Twig, needle and wood samples were collected four times during the year from both ponderosa pine (Pinus ponderosa) and white fir (Abies concolor). Soils were collected once. All samples were analyzed for Au and As and the wood samples were analyzed also for Sb.Arsenic was the best pathfinder element, having little analytical, spatial, or seasonal variation in the twig and needle samples. Anomalous levels were 150 μg/g (ppm) As in pine and 30 μg/g in fir. Gold showed analytical variation of 20–30%, sample duplicate variation up to 90%, spatial changes, and seasonal variation ranging from winter-summer background [10–20 ng/g (ppb) Au] to anomalies of 300–400 ng/g (ppb) Au in pine and 100 μg/g (ppb) Au in fir in the spring and fall. Antimony could not be completely evaluated as a pathfinder element because it was only determined in wood samples.Needles and twigs from both species proved to be viable sample media for exploration of the area. Wood was not a suitable medium because of low, erratic values, perhaps due in part to analytical technique. Needles had 2 to 20 times higher As concentrations than did twigs. Twigs had a slightly higher Au content [25 ng/g (ppb)] than did needles. The pine samples were higher in both elements than were the fir samples. The data, normalized by species, could be treated as one homogeneous data base.The soil Au and As data outlined the mineralization clearly with a central Au anomaly [100 ng/g (ppb) and greater] surrounded by As anomalies [100 μg/g (ppm) and greater] over a distance of 594 m. Neither spring nor fall tree Au anomalies were coincident with the soil Au anomaly. Consistent throughout the year, tree As anomalies coincided with the soil As anomalies, but covered a smaller area. Both the Au and As anomalies in trees appeared to be related to bedrock contact zones rather than to the soil the trees were growing in.  相似文献   

15.
Samples were collected near known gold mineralization from anomalous and background soils developed on glacial till in British Columbia and Ontario, and in residual soils in Nevada, Utah and the Yukon Territory. After wet sieving to five size fractions finer than 2000 mm, and separation of heavy minerals (S.G. > 3.3) for the − 212 + 106 μm and − 106 + 53 μm fractions, gold concentrations in each fraction were determined by fire assay-atomic absorption.In all cases more than 60% of the gold resides in the − 53 μm fraction. For the residual soils most of the remaining gold is associated with the light mineral fractions and only a negligible proportion resides in the heavy minerals. Estimates of the numbers of gold particles and subsampling variability suggest that gold, in both heavy and light mineral fractions, is largely present as inclusions of fine gold. For exploration purposes, optimum sample representativity would be obtained with the − 53 μm fraction. However, because this fraction is a major component of the soils, use of a coarser size fraction (e.g., − 212 μm) will only slightly reduce sample representativity. Also, because most of the gold is associated with the − 53 μm and light mineral fractions, use of heavy mineral concentrates offers no significant advantage and in some cases would result in anomalous conditions being overlooked.  相似文献   

16.
Pulverized coals from eleven power plants burning Central Appalachian coal blends and eight power plants burning Illinois Basin coal blends were studied in order to assess the petrographic nature of industrial-scale coal grinding. All coals were high volatile bituminous. Coals were wet screened at 100 (150 μ), 200 (75 μ), 325 (about 40 μ), and 500 (about 25 μ) mesh. Petrographic analysis of the whole coals and size fractions consisted of a combined maceral and microlithotype analysis. Microlithotype analysis, in particular, provides a reasonable approximation of the whole-particle composition at the scale of utility coal pulverization. In the size fractions, duroclarite, the most abundant trimaceral microlithotype, is most abundant in the coarsest fraction and least abundant in the finest fraction. Vitrite, the most abundant monomaceral microlithotype, exhibits the opposite trend. Duroclarite becomes more enriched in vitrinite towards the finer sizes. The partitioning of microlithotypes and the partitioning of macerals within the microlithotypes is indicative of the relative brittle nature of vitrite compared to the hard-to-grind trimaceral microlithotypes. Increased vitrinite in duroclarite is an indication that the microlithotype within the particular size fraction is more brittle than relatively vitrinite-depleted duroclarite in coarser fractions. The relative grindability of microlithotypes will, in turn, impact combustion efficiency.  相似文献   

17.
The triterpenol geochemistry of the Santa Monica Basin from the Southern California Borderland, off the U.S.A., is described from the study of two sets of trap deployments, five box cores (≈30 cm) and a hydroplastic core (≈1 m). The biogenic sources and diagenetic stability of the triterpenols are discussed.The 17β(H), 21β(H)-hopanols (22R isomer) occur in the carbon number range from 30 to 32 and their abundance is nearly uniform in the shallow sediment sections. However, the three hopanols follow the order of abundance, C32 > C31 C30, in deeper sections. Their concentrations spans from trace levels to 156 μg/g organic carbon (<15 ng to 7 μg/g dry sediment). Tetrahymanol (gammaceran-3β-ol) has been identified in all the samples except in one set of trap particles collected at 100 m water depth, from trace level (<1 μg) to 215 μg/g organic carbon (<20 ng to 9 μg/g dry sediment). Diplopterol is also detected in trace amounts in some samples. The triterpenols in the trap material generally increase with the water column depth and decrease with the subbottom depth in the sediment cores.The extended hopanols are either degradation products of polyhydroxybacteriohopanes or are biosynthesized by bacteria. Tetrahymanol is probably the only suggested biological precursor of gammacerane (the reduced counterpart of tetrahymanol), which has been recognized in numerous crude oils and lithified sediments. Although it has been reported earlier from Green River Shale and from a residual Pleistocene lake sediment, tetrahymanol has so far been positively identified from recent marine sediments only in two recent studies. The decreasing content of tetrahymanol in sedimentary depth profiles in the Santa Monica Basin would favor an origin for this compound in the water column or at the sediment surface. The ubiquitous occurrence of this compound throughout the study area suggests that this triterpenol most probably originates from primitive organisms (protozoa, bacteria?), hitherto not identified or, more likely, not yet analyzed for their lipid composition.  相似文献   

18.
Surface microlayer and subsurface water samples were collected at an oligotrophic Mediterranean site during a diel cycle. The composition of phospholipid ester-linked fatty acids (PLFA) was determined in size-fractionated particles (0.2–0.7 μm; 0.7–200 μm) in order to characterize the major contributors of organic matter to different size fractions. GF/F-retained particles (0.7–200 μm) from the surface microlayer were consistently enriched in PLFA relative to the underlying water. Molecular markers revealed a substantial difference in biological assemblages in both particle sizes. The larger particles were dominated by dinoflagellates, cyanobacteria, microzooplankton and attached bacteria, whereas particles filtered through GF/F and collected on 0.2 μm porosity Durapore filters (0.2–0.7 μm) were mostly bacteria and heterotrophic flagellates. Bacterial PLFA associated with 0.7–200 μm particles were more abundant than those in the 0.2–0.7 μm particles. Specific markers in the branched series appeared more representative of bacteria of smaller particle size.  相似文献   

19.
The focal point of this report is a bibliography of 133 references and an associated topic index — both of which could be useful to geochemists attempting to locate new Au deposits. Fifty of these references originated in the Soviet Union, where most of the initial work on biogeochemical exploration for Au had been done. The 15 topics in the index range from agriculture (Au in crop plants) to silver.As an introduction to the bibliography, we have briefly described some examples of applications and difficulties in using plants. These examples are drawn from the literature and from field experience. Because of the generally low Au concentrations found in plants, the analysis of plant tissue is critical to the successful application of the biogeochemical method of prospecting. Neuron activation analysis is the most widely used method to detect Au in plants, due largely to its sensitivity; levels in the parts per billion range are easily attained. Two general types of sampling media are used in prospecting for Au: humus and living plants. Humus has been widely used in Canada, but the sampling of plants has increased there and elsewhere in recent years. Our use of douglas-fir (Pseudotsuga menziesii) at a Au-bearing stockwork in Idaho is a prime example. A maximum Au concentration of 14 μg/g (ppm) was detected in the wood ash of this coniferous tree, well above the normal concentration of ≈ 0.15 μg/g. Among shrubs that might be useful in Au prospecting, we recommend sagebrush or wormwood (genus Artemisia), because it is extremely responsive to concealed mineralization. It has been used extensively in the Soviet Union and could be used in areas of the western United States where disseminated Au occurrences might be located.Among the problems one may encounter in using plants for Au prospecting are: (1) physiological barriers, by which many plant species simply do not absorb Au at detectable levels; (2) misconceptions of soil-plant correlations; (3) localization of Au in plant tissue; and (4) the variation of Au concentrations due to season. Despite these limitations, biogeochemical techniques can complement or replace other geochemical methods currently used.  相似文献   

20.
Gold anomalies in drainage sediments are often erratic, reflecting both the nugget effect and hydraulic effects whereby gold is concentrated at favorable sites along a stream. This study investigates these factors in a stream in northeastern Thailand.Bulk sediment samples, consisting of approximately 40 kg of −12 mm material, were collected from bar and pavement sites along an 8 km study reach. Samples were wet sieved into eight size fractions. The five fractions between 425 μm and 53 μm were then processed to obtain heavy mineral concentrates (SG > 3.3). Gold content of all size and density fractions finer than 425 μm was determined by fire assay-atomic absorption.Concentrations of Au in the heavy mineral concentrates typically range from 10,000 to 50,000 ppb (maximum 198,000 ppb), whereas the corresponding light mineral fractions and the −53 μm fraction generally contain <5 ppb gold. Within the heavy mineral fractions concentrations of Au generally increase downstream away from their supposed source and are higher at pavement than at point bar sites. Variations in abundance of gold between point bar sites can be related to stream characteristics (such as width, velocity and bed roughness) that are indicative of changing energy conditions and of the ability of the stream to winnow light minerals from its bed.The estimated median number of gold particles in the heavy mineral concentrates increase from less than one in the 212–425 μm fraction to about three in the 53–106 μm size range. However, because of dilution by the light mineral and −53 μm fractions, the probability of a 30 g analytical sub-sample containing a particle of gold is so low that in thirteen out of sixteen −149 μm sediment samples no gold was detected. Insofar as this results from dilution by large quantities of −53 μm sediment, failure of conventional sieved sediment samples to reliably detect the anomaly is probably a consequence of increased erosion caused by deforestation and land usage.Heavy mineral concentrates from pavement and other high energy sites are more reliable than conventional sediment samples for detecting gold anomalies of the Huai Hin Laep type. A low sample density is adequate but, because anomaly contrast may increase downstream, careful interpretation is required.  相似文献   

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