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1.
Gold mining activity in the Sierra Nevada foothills, both recently and during the California Gold Rush, has exposed arsenic-rich pyritic rocks to weathering and erosion. This study describes arsenic concentration and speciation in three hydrogeologic settings in the southern Mother Lode Gold District: mineralized outcrops and mine waste rock (overburden); mill tailings submerged in a water reservoir; and lake waters in this monomictic reservoir and in a monomictic lake developing within a recent open-pit mine. These environments are characterized by distinct modes of rock-water interaction that influence the local transport and fate of arsenic. Arsenic in outcrops and waste rock occurs in arsenian pyrite containing an average of 2 wt% arsenic. Arsenic is concentrated up to 1300 ppm in fine-grained, friable, iron-rich weathering products of the arsenian pyrite (goethite, jarosite, copiapite), which develop as efflorescences and crusts on weathering outcrops. Arsenic is sorbed as a bidentate complex on goethite, and substitutes for sulfate in jarosite.

Submerged mill tailings obtained by gravity core at Don Pedro Reservoir contain arsenic up to 300 ppm in coarse sand layers. Overlying surface muds have less arsenic in the solid fraction but higher concentrations in porewaters (up to 500 μg/L) than the sands. Fine quartz tailings also contain up to 3.5 ppm mercury related to the ore processing. The pH values in sediment porewaters range from 3.7 in buried gypsum-bearing sands and tailings to 7 in the overlying lake sediments. Reservoir waters immediately above the cores contain up to 3.5 μg/L arsenic; lake waters away from the submerged tailings typically contain less than 1 μg/L arsenic.

Dewatering during excavation of the Harvard open-pit mine produced a hydrologic cone of depression that has been recovering toward the pre-mining groundwater configuration since mining ended in 1994. Aqueous arsenic concentrations in the 80 m deep pit lake are up to 1000 μg/L. Redistribution of the arsenic occurs during summer stratification, with highest concentrations at middle depths. The total mass of arsenic in the pit lake increases coinciding with early winter rains that erode, partially dissolve, and transport arsenic-bearing salts into the pit lake.

Arsenic concentration, speciation, and distribution in the Sierra Nevada foothills depend on many factors, including the lithologic sources of arsenic, climatic influences on weathering of host minerals, and geochemical characteristics of waters with which source and secondary minerals react. Oxidation of arsenian pyrite to goethite, jarosite, and copiapite causes temporary attenuation of arsenic during summer, when these secondary minerals accumulate; subsequent rapid dissemination of arsenic into the aqueous environment is caused by annual winter storms. As the population of the Mother Lode area grows, it is increasingly important to consider these effects during planning and development of land and groundwater resources.  相似文献   

2.
Groundwater pollution by arsenic is a major health threat in suburban areas of Hanoi, Vietnam. The present study evaluates the effect of the sedimentary environments of the Pleistocene and Holocene deposits, and the recharge systems, on the groundwater arsenic pollution in Hanoi suburbs distant from the Red River. At two study sites (Linh Dam and Tai Mo communes), undisturbed soil cores identified a Pleistocene confined aquifer (PCA) and Holocene unconfined aquifer (HUA) as major aquifers, and Holocene estuarine and deltaic sediments as an aquitard layer between the two aquifers. The Holocene estuarine sediments (approximately 25–40 m depth, 9.6–4.8 cal ka BP) contained notably high concentrations of arsenic and organic matter, both likely to have been accumulated by mangroves during the Holocene sea-level highstand. The pore waters in these particular sediments exhibited elevated levels of arsenic and dissolved organic carbon. Arsenic in groundwater was higher in the PCA (25–94 μg/L) than in the HUA (5.2–42 μg/L), in both the monitoring wells and neighboring household tubewells. Elevated arsenic concentration in the PCA groundwater was likely due to vertical infiltration through the arsenic-rich and organic-matter-rich overlying Holocene estuarine sediments, caused by massive groundwater abstraction from the PCA. Countermeasures to prevent arsenic pollution of the PCA groundwater may include seeking alternative water resources, reducing water consumption, and/or appropriate choice of aquifers for groundwater supply.  相似文献   

3.
Uraniferous Holocene sediments occur in the Carson Range of Nevada and California, U.S.A., between Lake Tahoe and Carson Valley. The hosts for the uranium include peat and interbedded organic-rich sand, silt, and mud that underly valley floors, fens, and marshes along stream valleys between the crest of the range and the edge of Lake Tahoe. The known uranium accumulations extend along the Carson Range from the area just southeast of South Lake Tahoe northward to the area just east of Carson City; however, they almost certainly continue beyond the study area to the north, west, and south. Due to the young age of the accumulations, uranium in them is in gross disequilibrium with its highly radioactive daughter products. These accumulations have thus escaped discovery with radiation detection equipment in the past. The uranium content of these sediments approaches 0.6 percent; however, the average is in the range of 300–500 ppm. Waters associated with these sediments locally contain as much as 177 ppb uranium. Modest levels of helium and radon also occur in these waters.Uraniferous waters are clearly entering the private and public water supply systems in some parts of the study area; however, it is not known how much uranium is reaching users of these water supplies. Many of the waters sampled in the study area exceed the published health effects guidance level of the Environmental Protection Agency. Regulatory standards for uranium in waters have not been published, however.Much uranium is stored in the sediments along these stream valleys. Estimates for a marsh and a fen along one drainage are 24,000 and 15,000 kg, respectively. The potential effects of man-induced environmental changes on the uranium are uncertain. Laboratory studies of uraniferous sediment rich in organic matter may allow us to evaluate the potential of liberating uranium from such sediments and creating transient increases in the level of uranium moving in water in the natural environment.  相似文献   

4.
A pilot area within the Venetian Plain was selected to assess the arsenic (As) contamination of groundwater. The area represents a typical residential, industrial and agricultural organization representative of most western countries, and is also devoid of lithologies with high or anomalous As content. Hydrogeological and chemical data have been collected, the latter spatialized by a geostatistical approach. The unconfined aquifer reservoir varies from a predominantly gravel composition in the north to a sandy and silt–clay composition further south, including peat layers. The hydrochemical features of the waters are rather homogeneous, featuring low mineral content and a Ca-bicarbonate signature. In contrast, the redox state is highly variable; oxidizing conditions are predominant in the northern and coarse parts of the aquifer, whereas reducing potentials prevail in the southern and silt–clay parts. Several well waters contain arsenic in excess of drinkable limits (=10 ppb), and most of these wells are located in the southern area. A large portion of the studied area has a high probability of containing non-potable water (up to 150 ppb As). Remarkably, As “hot spots” (As > 300 ppb, up to 431 ppb) were identified at the transition from gravel to silt–clay sediments. No industrial or agricultural source of As has been found.  相似文献   

5.
Groundwater in some deep wells of Maydavood aquifer, southwestern Iran, contains relatively high concentrations of arsenic. Detailed hydrochemical analysis of these groundwaters (with ICP-OES instrument) showed that concentrations of iron, manganese, nickel, and vanadium are also high in them and concentrations of total arsenic in 81% of deep wells are greater than World Health Organization’s permissible value (10 ppb). XRF analysis of surrounding geological formations and aquifer sediments proposed that original source of arsenic in aquifer material can be attributed to minerals from Asmari Formation. It appears that a key mechanism for arsenic mobilizing to deep wells is microbial biodegradation of petroleum related organic matters (PROMs), which exist in aquifer sediments and originates from the bedrock of the aquifer (Gachsaran Formation). This process is followed by microbially mediated reductive dissolution of arsenic-bearing iron/manganese oxyhydroxides/oxides and further by nickel and vanadium mobilizing to groundwater. According to hydrogeochemical conditions and cluster analysis, water wells in Maydavood aquifer are divided to four subgroups: the wells with mildly reducing condition (subgroup I), moderately reducing condition (subgroup II), reducing condition (subgroup III), and high reducing condition (subgroup IV). Affected wells to arsenic are belonged to subgroups III and IV.  相似文献   

6.
 The aquifer system of the Upper Triassic Keuper Sandstone, an important source of drinking water in northern Bavaria, is affected by elevated arsenic concentrations. Within the study area of 8000 km2, no evidence exists for any artificial source of arsenic. Data from about 500 deep water wells show that in approximately 160 wells arsenic concentrations are 10–150 μg/L. The regional distribution of arsenic in the groundwater shows that elevated arsenic concentrations are probably related to specific lithofacies of the aquifers that contain more sediments of terrestrial origin. Geochemical measurements on samples from four selected well cores show that arsenic has accumulated in the rocks. This indigenous arsenic is the source of arsenic in the groundwater of certain facies of the middle unit of the Keuper Sandstone. Received, June 1998 / Revised, January 1999, May 1999 / Accepted, June 1999  相似文献   

7.
High arsenic levels in groundwater of the aquifers, belonging to the Pliocene terrestrial layers and Quaternary alluvial sediments, have become a significant problem for the inhabitants living in Sarkisla (Turkey). The main objective of this study was to determine the origin and arsenic contamination mechanisms of the Sarkisla drinking water aquifer systems. The highest arsenic concentrations were found in Pliocene layers and alluvial sediments with concentrations ranging from 2.1 to 155 mg/kg. These rocks are the main aquifers in the study area, and most of the drinking groundwater demand is met by these aquifers. Groundwater from the Pliocene aquifer is mainly Ca-HCO3 and Ca-SO4 water type with high EC values reaching up to 3,270 μS/cm, which is due to the sulfate dissolution in some parts of the alluvial aquifer. Stable isotope values showed that the groundwater was of meteoric origin. Tritium values for the groundwater were between 8.31 and 14.06 TU, representing a fast circulation in the aquifer. Arsenic concentrations in the aquifers were between 0.5 and 345 μg/L. The highest arsenic concentrations detected in the Pliocene aquifer system reached up to 345 μg/L with an average value of 60.38 μg/L. The arsenic concentrations of the wells were high, while the springs had lower arsenic concentrations. These springs are located in the upper parts of the study area where the rocks are less weathered. The hydrogeochemical properties demonstrated that the water–rock interaction processes in sulfide-bearing rocks were responsible for the remarkably high groundwater arsenic contamination in the study area. In the study area, the arsenic levels determined in groundwater exceeded the levels recommended by the WHO. Therefore, it is suggested that this water should not be used for drinking purposes and new water sources should be investigated.  相似文献   

8.
Spatial distribution and temporal trends studies were carried out at Katedan Industrial Development Area (KIDA) near Hyderabad, capital of Andhra Pradesh state, India under Indo-Norwegian Institutional Cooperation Program, to find out the extent of contamination in streams and lake sediments from the discharge of industrial effluents. Stream and lake sediment samples were collected from the five lakes in the study area and connecting water streams. The samples were analyzed by XRF spectrometer for toxic elements. The studies reveal that the stream sediments with in the KIDA and the impounded Noor Mohammed Lake down stream have high concentration of some of the toxic elements like chromium, nickel, lead, arsenic, zinc etc. The geology of the area indicates that the study area consists of residual soil of acidic rocks, which are predominantly of Archaean gneisses and granites having low to medium concentrations of chromium and nickel. The source of these high concentration of elements like lead 2,300 mg/kg, copper 1,500 mg/kg, arsenic 500 mg/kg, chromium 500 mg/kg etc. cannot be derived from the surrounding acidic rocks and may be attributed to the industrial effluents released in the ditches and random dumping of hazardous solid waste. It was observed that the metal concentrations increased in the streams during the dry season (pre-monsoon period). After the monsoon rains, the metal concentrations in the streams were reduced by half which may be due to dilution. The eroded sediments are deposited in the lake where very high concentrations were encountered. Overflowing of the lake will spread the contamination further downstream. The lake sediments will remain as a major source of contamination by desorption to the water phase regardless of what happens to the effluent discharge in the KIDA. However, some samples showed enrichment of lead, arsenic and nickel during post-monsoon, which were collected near the dumpsite due to the leaching of toxic elements from the dump site to the lakes. Some of the toxic elements like nickel and copper have not shown any dilution but have increased after the rains, which could be due to the leaching of arsenic from the dumpsite to the lake along with rainwater. Geochemical maps showing the distribution of heavy/trace elements in streams and lakes are prepared and presented in this paper. Effect of toxic elements on the health of the residents in the surrounding residential areas is also discussed.  相似文献   

9.
High As contents in groundwater were found in Rayen area and chosen for a detailed hydrogeochemical study. A total of 121 groundwater samples were collected from existing tube wells in the study areas in January 2012 and analyzed. Hydrogeochemical data of samples suggested that the groundwater is mostly Na–Cl type; also nearly 25.62 % of samples have arsenic concentrations above WHO permissible value (10 μg/l) for drinking waters with maximum concentration of aqueous arsenic up to 25,000 μg/l. The reducing conditions prevailing in the area and high arsenic concentration correlated with high bicarbonate and pH. Results show that arsenic is released into groundwater by two major phenomena: (1) through reduction of arsenic-bearing iron oxides/oxyhydroxides and Fe may be precipitated as iron sulfide when anoxic conditions prevail in the aquifer sediments and (2) transferring of As into the water system during water–acidic volcanic rock interactions.  相似文献   

10.
Geochemical stream sediment survey in Winder Valley, Balochistan, Pakistan   总被引：1，自引：0，他引：1  
A pilot scale geochemical survey of sediments from the Winder Stream (SW Pakistan) and its tributaries was carried out. The Winder Stream mainly receives sediment from the southern extensions of the Mor and Pab Ranges in the District of Lasbela (Balochistan). In these two mountain ranges, rocks from Jurassic to Cretaceous age are exposed. Rocks of the Ferozabad Group comprise of carbonates and siliciclastics of Lower–Middle Jurassic age and occupy the dominant part of the Mor Range. These strata host syngenetic and epigenetic Zn–Pb–Ba mineralizations of Stratiform Sediment-Hosted (SSH) and Mississippi Valley Type (MVT) deposits.Quantitative estimates of mobile and immobile elements were made from active stream sediments of the Winder stream and its tributaries. The samples were analyzed for Ag, Zn, Pb, Cu, Ni, Co, V, Mn, Fe and Ba using atomic absorption spectroscopy. The abundance of these elements is discussed in relation to local geological conditions such as bedrock, climate, weathering, mobility and pH of the dispersing waters. A number of Zn anomalies have been distinguished in the study area. Kharrari (Zn, 360 ppm), Sand (Zn, 340 ppm) and Draber (Zn, 210 ppm) are demarcated as new areas for Zn mineralization. The present study also indicates prospects of Ag, Cu and V in the rocks of the Mor Range.Relationships between various elements have been identified from scattergrams and reflect genetic associations. Whereby the positive correlation between Cu–Zn (0.55, n=18) and Cu–Pb (0.63) is related to possible sulphide mineralization.  相似文献   

11.
 Interaction of groundwater with As-bearing rocks has been proposed as one of three main sources of arsenic at Zimapán valley, México. The complexity of the geology and hydrogeology of the valley make it difficult to identify the natural causes of arsenic poisoning. Samples from the different rock outcrops and water from wells tapping various rock formations were analyzed. The rocks from mineralized areas contained higher concentrations of arsenic with respect to the same formations in non-mineralized areas. The arsenic minerals arsenopyrite, scorodite, and tennantite were identified in some rock samples. Higher temperature and lower Eh values were found for those wells containing more arsenic. The physicochemical characteristics of these naturally polluted well waters could be produced by arsenopyrite oxidation. The geochemical model PHREEQCI was used to perform the inverse modeling of two wells located along the same fault. Arsenopyrite oxidation and scorodite dissolution appear to be the geochemical processes producing the natural pollution according to the model. The release and transport of arsenic mainly occur through fractures within the cretaceous limestones where the most productive wells are drilled. The presence of arsenic should be expected also in other formations near mineralized zones in the Zimapán Valley. Field determinations of Eh and T could be used to detect potentially polluted wells. Received: 29 April 1999 / Accepted: 18 July 2000  相似文献   

12.
《Applied Geochemistry》2006,21(9):1482-1497
Population statistics for As concentrations in rocks, sediments and ground water differ by geology and land use features in the New England region, USA. Significant sources of As in the surficial environment include both natural weathering of rocks and anthropogenic sources such as arsenical pesticides that were commonly applied to apple, blueberry and potato crops during the first half of the 20th century in the region. The variation of As in bedrock ground water wells has a strong positive correlation with geologic features at the geologic province, lithology group, and bedrock map unit levels. The variation of As in bedrock ground water wells also has a positive correlation with elevated stream sediment and rock As chemistry. Elevated As concentrations in bedrock wells do not correlate with past agricultural areas that used arsenical pesticides on crops. Stream sediments, which integrate both natural and anthropogenic sources, have a strong positive correlation of As concentrations with rock chemistry, geologic provinces and ground water chemistry, and a weaker positive correlation with past agricultural land use. Although correlation is not sufficient to demonstrate cause-and-effect, the statistics favor rock-based As as the dominant regional source of the element in stream sediments and ground water in New England. The distribution of bedrock geology features at the geologic province, lithology group and map unit level closely correlate with areas of elevated As in ground water, stream sediments, and rocks.  相似文献   

13.
Lack of high-spatial-resolution soil and sediment arsenic data for Hawai‘i has generated substantial disagreement between researchers and regulators regarding the magnitude of natural levels of arsenic in Hawai‘i and rendered difficult the defining of areas of anthropogenically elevated arsenic. Our earlier research into the occurrence of arsenic in terrestrial and marine environments revealed widely disparate concentrations of arsenic with no apparent spatial pattern. To better understand the distribution and abundance of arsenic in soils and sediments of O‘ahu, we collected an additional 64 samples at locations chosen to represent different environments with varying degrees of human impact. We found surface arsenic values that ranged from 0.28 to 740 ppm with a median concentration of 8.1 ppm, which is above the global median of 5 ppm and US soil median of 5.2 ppm. Higher concentrations of arsenic (up to 913 ppm) were encountered at depth in soil cores. The median arsenic in streambed sediments from one of our earlier studies of 6.1 ppm was comparable to the conterminous US median of 6.3 ppm; however, we encountered arsenic concentrations as high as 43.9 ppm (median = 8.60 ppm, n = 75) in marine sediments in recent work off the leeward coast of O‘ahu. Overall, arsenic in the soils and sediments of O‘ahu is elevated relative to world and national values, but there still is no readily discernible pattern in the distribution of arsenic to explain these elevated values.  相似文献   

14.
The Yunnan-Guizhou-Guangxi region is well known for its abundant mineral resources, and low-temperature hydrothermal mineralization represented by the elemental association of gold, arsenic, antimony and mercury is widely developed there. Many studies on the geological-geochemical characteristics of gold have been conducted, but a comprehensive understanding of the antimony geochemical pattern is still lacking. This paper studied the Sb distribution characteristics and the cause of geochemical anomalies based on the geochemical data of stream sediments and rocks in the study area. In addition, the geochemical data of Au, As, Sb and Hg were centered and log-ratio transformed to eliminate the closure effect, and then random forest regression (RFR) with Au, As and Hg as the characteristic variables was used to investigate the ore-related geochemical anomalies of Sb. Seven geochemical provinces were delineated from the original geochemical data, and they are not entirely consistent with the known deposits. Sb moves from the rocks to the stream sediments during weathering. The variation trend in the Sb background values in stream sediments in each tectonic unit is consistent with that in the rocks themselves, implying that Sb in the stream sediments is inherited from the background rocks. The distributions of Sb predicted by RFR are similar to the distribution pattern of Sb in stream sediments. Of the three elements considered, the influence of As on the variations in the Sb geochemical background is the greatest, followed by Au and then Hg. The geochemical anomalies extracted by the residuals produced in this algorithm are consistent with where the known Sb metallogenic district is located, indicating that this method of recognizing geochemical anomalies is feasible and effective and has theoretical and practical significance.  相似文献   

15.
The Iron Quadrangle has been the scenery of the most important gold production in Brazil. It is estimated that during the three centuries of gold mining in the Iron Quadrangle, at least 390,000 t of arsenic was discharged into the drainage system. This study presents geochemical data for the three river basins in the region, with focus on surface water and stream sediment monitoring. Samples of primary and oxidized sulfide ores as well as of tailings and groundwater from the major gold mines were also studied. The highest As concentrations in water and stream sediments occur in the vicinity of mining areas. In surface water, up to 300 g As/l were found whereas the As contents in stream sediments were in the range of 20 to 4,000 mg/kg. The As3+/As5+ concentration ratios obtained for some water samples range from 1.10у to 4.10ф. The As mobility associated with ore-deposit weathering could be traced in some closed gold mines by observation of in-situ pyrite and arsenopyrite oxidation, precipitation of scorodite and gippsite, As adsorption onto goethite, and final liberation of As into underground and surface waters. This process is likely to produce large volumes of mine effluents containing total As and trivalent As up to 1,960 and 60 g/l, respectively. River sediments and tailings pile samples were submitted to a leaching procedure showing maximal arsenic release from 1 to 4% of the original total As in the samples. There are potential risks for As hazards in some areas induced by, for instance, the dispersion of old tailings by flooding, occupation of poisoned soils for settlements, and occasional consumption of contaminated surface and groundwater.  相似文献   

16.
A reconnaissance exploration survey over 14 000 km2 of Precambrian terrain in South Greenland using stream-sediment and stream-water samples delineated a central uranium district of 2000 km2 with enhanced uranium levels and smaller anomalous zones in the south of the field area.The area is underlain by Archean and Proterozoic gneisses, granites and metasediments all of which have been intruded by late Proterozoic alkaline intrusions (Gardar Province). The terrain is mountainous and the streams are either steep torrents or impeded drainages typical of glaciated terrains with boggy organic rich sediments.The central uranium district was defined by a high uranium background in both stream sediments (5–20 ppm) and stream waters (0.5–1.0 ppb) and a markedly higher frequency of very anomalous values in the order of 50–100's ppm in the stream sediments and 1–10 ppb in the stream waters. An areal correlation of uranium, in this district, with high pH and conductivity in the stream water in addition to a higher organic content noted in the stream sediment raised the question of a possible enhancement of uranium values due to secondary environmental effects. On the other hand, an areal correlation of uranium with niobium and other trace elements characteristically associated with alkaline rocks, and the geographic proximity of this uraniferous district to the alkaline intrusions suggested a genetic relationship between uranium mineralization and the alkaline igneous activity.Limited follow-up work located 8 pitchblende occurrences in this extensive district. The pitchblende is in veins which contain quartz, calcite, iron oxide, fluorite and minor sulphides. The isotopic (U-Pb) age of the pitchblende, which ranges from 1180-1090 Ma, corresponds to the late stages of Gardar alkaline igneous activity. It is concluded, therefore, that the reconnaissance geochemistry reflects a district-wide hydrothermal event related to the late volatile differentiates derived from the highly fractionated alkaline magma. A combination of primary and secondary features have complemented each other in enhancing the geochemical reconnaissance data and emphasized its importance but has not materially altered the interpretation.The south of the field area also has a relatively high uranium background in both the sample media with some discrete anomalous zones, usually with a slightly lower order of magnitude than the central area, but still with a distinct contrast of 5–10 times. Fine-grained uraninite has been found in the area occurring as disseminated grains in pegmatitic elements as in the central district. Isotopic ratios (U-Pb) suggest an age of 1728 ± 30 Ma which probably reflects the long cooling of the granite.It is concluded that the geochemical reconnaissance data delineated two uranium metallogenic districts characterized by distinctly different types of uranium mineralization. It is suggested that South Greenland may be part of a much wider uranium geochemical province which includes parts of Labrador. To the present plate-tectonic models, which suggest such a connection (Le Pichon et al., 1977), must be added the comparable reconnaissance geochemical results (G.S.C. Open Files nos. 748 and 749), and the similar 1730 Ma age of the Kitts uranium mineral occurrence in Labrador (Gandhi, S.S , 1978) to that of the uraninite found in the south of the field area in Greenland.  相似文献   

17.
The Chinkuashih is a group of dacite-related hydrothermal enargite-gold deposits of the Quaternary age, which produced 94 tons of gold and 119,101 tons of copper from 1895 to 1987. It has remaining reserves of 656 tons of gold with an average grade range of 1.5–3.5 g/ton of Au for all orebodies discovered.Mercury content in different media such as stream sediments, heavy minerals in stream sediments, soils, rocks/ores, and pyrite samples was analyzed by a gold–film mercury detector to evaluate whether mercury is a good pathfinder for these types of deposits at Chinkuashih. The gold film technique is more rapid and cheaper than the traditional fire assay or fire assay/ICP-MS gold and trace element analyses.Mercury in stream sediments and soils indicated the border zone of gold mineralization 12 km away from the center of mineralization at Chinkuashih. Mercury in heavy minerals of the stream sediments distinguished the intermediate zone with gold veins and gold/gold–copper breccia pipes from the core or inner zone with the gold–copper zone. It has been found that contours of 1000 or 500 ppb Hg of soil samples can delineate the outcropping gold orebodies. The gold ores generally contain 1000 ppb or more Hg.  相似文献   

18.
Low-temperature thermal waters (<20–40 °C) from Mesozoic carbonate formations of Outer and Inner Dinarides which outcrop along the margins of small Tertiary basins, are characterised by low content (commonly <500 mg/l) of total dissolved solids and the dominance of calcium-(magnesium) bicarbonate hydrogeochemical facies. Trace elements occur in the ppb to ppt range, and can be substantially enriched in carbon dioxide-rich thermomineral waters. Contacts of thermal waters with clastic sediments affect the abundance of many trace elements, like B, Ni, Mn, Fe, Se, Sr, Ba, REE and Th. The U/Th ratios are commonly very high for the waters from carbonate aquifers, although the U abundance is in the range of some ppb. The influence of clastic sediments is reflected in an increased abundance of Th, and therefore much lower U/Th ratio. Some waters are rich in strontium (over 1 ppm), which probably originates from aragonite in Cretaceous carbonate rocks.  相似文献   

19.
A new method of simultaneous multi-elemental analysis, Proton Induced X-ray Emission (PIXE), was used to detect trace elements in waters associated with a coal strip-mining operation in southern Indiana. Stream, pond, and ground water samples were collected and analyzed monthly from, or near, Sulphur Creek in Sullivan County. The concentrations of 26 major and trace elements were determined in samples from eleven locations: K, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, As, Se, Br, Rb, Sr, Mo, Cd, Sn, Sb, I, Ba, Hg, Pb, and U. Elemental concentrations fluctuated considerably throughout the 13-month sampling period and also among sampling sites. Nickel, Zn, As, Cd, Mn, Fe, and Ca were highest in the upstream water which was most acidic (pH = 2.9–4.0) because of old unreclaimed mining operations. The highest values recorded were Ni = 1662 ppb, Zn = 4953 ppb, As = 26 ppb, Cd = 93 ppb, Mn = 5063 ppb, Fe = 63 ppm, and Ca = 325 ppm. The concentrations of these elements decreased downstream as the pH of Sulphur Creek increased which was likely due to the influence of the calcareous glacial till cover in the area and the recent mining activity which disturbed overburden containing a high percentage of calcareous materials. Lead, I, Br, and Ti values were highest (661 ppb, 86 ppb, 70 ppb, and 45 ppb, respectively) in the ground water from the coal seam (pH approximately 7). Other elements which were relatively high in the pH 7 waters closest to the current mining operations (pond, stream, and groundwater) included K (17 ppm), Sr (3408 ppb), Ba (173 ppb), As (14 ppb), Rb (16 ppb), Sn (14 ppb), and Cu (3840 ppb). The highest Cu concentration was recorded at the point where drainage water from the mine entered Sulphur Creek. Gallium, U, Hg, and Mo were found in low (< 13 ppb for Ga and Hg; < 205 ppb for Mo and U) concentrations and only in the ponds within the mine.  相似文献   

20.
Overbank and medium-order stream sediment samples were collected in Belgium and Luxembourg from 66 sampling locations (area of about 33,000 km2) and analysed for major and trace elements among which Zn, Pb, Cu and As. At each sampling location large bulk samples were taken, namely in the lower (normally at ≥1.5 m depth, over an interval of about 20–40 cm) and upper (normally upper 5–25 cm) parts of the overbank profiles and from the stream sediments. Furthermore, at a number of these sites, a detailed geochemical analysis of vertical overbank sediment profiles (sampling intervals of 10–20 cm) was subsequently carried out to unravel element variations through time and to help in the overall evaluation. For most sampled sections evidences such as 14C-dating and the absence of anthropogenic particles point towards a pre-industrial and often pristine origin of the lower overbank sediment samples. From the latter bulk samples, mean background concentrations were deduced. They reveal the existence of significant differences between the northern and southern part of Belgium (incl. Luxembourg) which relate to the difference in geological substrate. In the north dominantly non-lithified Quaternary and Tertiary sands, marls and clays occur while in the south Palaeozoic sandstones, shales and carbonate rocks outcrop. Consequently separate mean background values were calculated for the two areas. In the southern study area, some anomalous metal concentrations have been recorded in pre-industrial sediments. They are derived from mineralised Palaeozoic rocks, a feature which could be of interest for base metal exploration. In the upper overbank and stream sediments, in general, higher heavy metal and As contents were recorded with highest values in areas with metal mining, metal melting and cokes treatment industries. By comparing the trace element concentrations of the upper overbank or stream sediment samples with the concentrations detected in the lower overbank samples at each of the sampling locations, and by evaluating the vertical distribution patterns where available, the degree of pollution of the alluvial plain and the present-day stream sediments can be assessed. From this exercise, it is clear that highest pollution occurs in the northern part of Belgium, which relates to its high population density and industrial development.  相似文献   

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