Low-density geochemical mapping in Portugal

This paper reports the first results of a low-density geochemical survey covering the whole continental area of Portugal, taking both topsoils and active stream sediments as the sampling media. The data were obtained in a consistent way from 653 sites at a sampling density of 1 site/135 km². The samples were analysed for 31 elements by ICP-AES and after quality control the following 19 were selected: Al, As, Ba, Ca, Co, Cr, Cu, Fe, K, La, Mg, Mn, Ni, P, Pb, Sr, Th, V and Zn. The baseline levels for these elements are presented. The first geochemical maps of Portugal were prepared and the geochemical patterns are generally well correlated to geological factors sometimes combined with anthropogenic influences. Some general trends can be observed between geochemical patterns and soils distribution.     

Particulate trace metal speciation in stream sediments and relationships with grain size: Implications for geochemical exploration

Sediment samples were collected from streambeds in an undisturbed watershed in eastern Quebec (Gaspé Peninsula). Two sampling sites were located on a stream draining an area of known mineralization (Cu, Pb, Zn) and two on a control stream. The sediment samples were separated into 8 distinct size classes in the 850 μm to <1 μm size range by wet sieving, gravity sedimentation or centrifugation. Each sediment subsample was then subjected to a sequential extraction procedure designed to partition the particulate heavy metals into five fractions: (1) exchangeable; (2) specifically adsorbed or bound to carbonates; (3) bound to Fe-Mn oxides; (4) bound to organic matter; (5) residual. The following metals were analyzed in each extract: Cu, Pb, Zn; Fe, Mn.Comparison of samples from the mineralized area with control samples revealed the expected increase in total concentrations for Cu, Pb and Zn. Non-detrital metals were mainly associated with Fe oxides (specifically adsorbed; occluded) and with organic matter or resistant sulfides. For a given sample, variation of trace metal levels in fractions 2 and 3 with grain size reflected changes in the available quantities of the inorganic scavenging phase (FeOx/MnOx); normalization with respect to Fe and Mn content in fraction 3 greatly reduced the apparent dependency on grain size.The results of this study suggest that a single reducing extraction (NH₂OH.HCl) could be used advantageously to detect anomalies in routine geochemical surveys. A second leaching step with acidified H₂O₂ could also be included, as the trace metal concentrations in fraction 4, normalized with respect to organic carbon content, also showed high {anomaly/background} ratios.     

Partitioning of manganese,iron, copper,zinc, lead,cobalt, and nickel in black coatings on stream boulders in the vicinity of the Magruder mine,Lincoln Co., Georgia

Sequential digestions of Fe-Mn oxide coated boulders collected upstream and downstream from the Magruder mine, Lincoln Co., Georgia, indicate probable partitioning relationships for Zn, Cu, Pb, Co, and Ni with respect to Mn and Fe. Initial digestion with 0.1M hydroxylamine hydrochloride (Hxl) in 0.01M HNO₃ selectively dissolyes Mn oxides, whereas subsequent digestion with 1:4 HCl dissolves remaining Fe oxides.The results indicate that partitioning is not constant, but varies systematically with respect to the location of metal-rich waters derived from sulfide mineralization. Upstream from the mineralized zone Zn and Ni are distinctly partitioned to the Fe oxide component and Co and Cu are partitioned to the Mn oxide component. Immediately downstream from the mineralized zone, Mn oxides become relatively more enriched in Zn, whereas Fe oxides are relatively more enriched in Cu, Co, and Ni. Analytical precision for Pb is poor, but available data suggests it is more closely associated with Fe oxides.For routine geochemical surveys utilizing coated surfaces, a one-step digestion method is probably adequate. Parameters useful for detecting sulfide mineralization are metal concentrations normalized to surface area or various ratios (e.g. Zn/(Mn + Fe), Cu/Mn, Pb/Fe). Ratios can be obtained much faster, and at lower analytical costs than conventional analysis of stream sediment.     

Heavy metals in stream sediments: Effects of human activities

The content of 11 heavy metals in the sediments of a stream system was determined by atomic absorption analysis. Geochemical phases were investigated using a sequential extraction scheme, and bulk contents were assessed with a single HNO₃ extraction. Certain heavy metals were associated with different geochemical phases. Co, Mn, and Ba concentrated primarily in the carbonate and Mn phases, while all the remaining metals concentrated in the Fe and remnant phases. Features located along the stream system influenced the content of heavy metals. Results from the geochemical phases indicated Cu, Pb, Zn, Cd and Ag were emitted by one landfill, while Cd, Ba, and Ag were emitted by a second landfill. A wastewater treatment facility appeared to emit Ni and Cu. A stream draining a reservoir and joining the study stream resulted in dilution of the heavy metals in the sediments. A populated area along the study stream appeared to emit Mn. The single HNO₃ extraction procedure is quicker to perform than the sequential extraction but does not indicate the phase associations.     

水系沉积物和典型土壤剖面地球化学试验--以江西九岭钨铜多金属矿集区为例

为了在成矿区带和矿集区找矿工作中有所突破,开展工作区内水系沉积物和土壤剖面地球化学的试验是一项不容忽视的工作。江西九岭钨铜多金属矿集区水系沉积物、典型土壤剖面地球化学试验表明：①在赣北九岭地区寻找岩浆热液型钨、铜多金属矿床的最佳指示元素是W、Sn、Cu、Mo、Bi、Ag、Cd、F;②地球化学普查（1∶25万-1∶5万）水系沉积物的采样位置应以一级水系的采样为主,辅以少量二级水系,采样粒度以10～60目的水系沉积物为宜;③地球化学详查（1∶5000-1∶10000）土壤地球化学测量采样层位为残积土壤B层,采样深度为20～40cm,采样粒度20～40目,或小于40目均可显示出较好的异常。     

Comparison of stream sediment and soil sampling for regional exploration in the eastern Alps,Austria

Tests in three different areas of the Austrian Alps showed that in mountainous areas, soil samples taken at the break of slope are an alternative sampling medium to stream sediments for regional geochemical exploration even if taken at the unusually low density of 1 sample/km². B-horizon soil samples from the nearest break of slope were collected in conjunction with stream sediment orientation studies. The minus 0.2 mm fraction of all samples was routinely analyzed for the total contents of 36 elements. The results for the indicator elements in the three test areas (Area 1: Cu; Area 2: Ag, As, Cu, Pb, Sb, Sn, Zn; Area 3: As, Cu) showed that break-of-slope soil samples more clearly indicate known mineralization than drainage geochemistry. In the soils, almost all elements showed a higher natural variability of the data with considerably higher metal contents. In mountaineous regions, each soil sample will have a clearly defined area of influence. The break of slope represents a site where clastically and hydromorphically dispersed elements are concentrated. It is concluded that soil samples can be used for regional exploration using low sampling densities in mountaineous areas. At the same time they will provide valuable information for other fields of science (e.g. agriculture, forestry, environmental sciences) and are thus superior to stream sediments.     

Multi-element,multi-medium regional geochemistry in the European Arctic: element concentration,variation and correlation

A multi-medium, multi element regional geochemical survey has been carried out in an 188,000 km² area in the Central Barents Region, Finland, Norway and Russia. Four different sample materials (terrestrial moss, O-, B- and C-horizons of podzol) were collected at the same sites throughout the area at a density of 1 site/300 km². While moss predominantly reflects the atmospheric input of elements, the O-horizon reflects the complex interplay between atmosphere, biosphere and lithosphere. The B-horizon can be used to study the influence of soil-forming processes, while the C-horizon represents the composition of the lithosphere at each sample site and thus the geogenic background. The concentration, variation and correlation between 24 elements (Ag, Al, As, Ba, Bi, Ca, Cd, Co, Cu, Fe, K, Mg, Mn, Na, Ni, P, Pb, S, Si, Sr, Th, V, Zn) analysed with similar techniques in all 4 materials are compared. Some rare trace elements (Ag, As, Bi, Cd, Pb) appear to be considerably more enriched in the O-horizon of podzols than the main pollutants in the survey area (Ni, Cu, Co from the Russian nickel industry in Monchegorsk and Nikel-Zapoljarnij). Biological processes play an underestimated role in determining regional geochemistry at the earth's surface.     

Regional geochemical reconnaissance in the Belgian Ardennes: Secondary dispersion patterns in stream sediments

Two geochemical stream sediment surveys were conducted in the Belgian Ardennes for Fe, Cu, Pb, Zn, Co, Ni and Mn. The geological setting is of quartzo-pelitic rocks of Early Devonian and Cambro-Ordovician age. One survey covers the Ourthe and Salm valleys, the other the Lesse and Lomme drainage basins. Results of these surveys show the geochemical similarity of the two regions. Anomalies have been ascribed to four factors: human activity, Fe-Mn enrichment, known mineralization and potential mineralization. Mean values of metal concentration and statistical dispersion are identical. This results from similar physico-chemical conditions which induce the same types of surficial metallic association. The stream environment is characterized by two main phases, an oxidizing phase where Fe-Mn oxides trap trace metals, and a reducing phase where organic matter and secondary sulphides are bound with Pb, Zn and Cu. In oxidizing conditions, Cu and Ni show a greater affinity for the Fe-oxides while Zn and especially Co are related to the Mn-oxides. Pb has only a weak relationship with the Fe-Mn oxides but is also associated with the organic matter and the secondary sulphides in the reducing environment. Consequently, one may propose the following scale of mobility: Zn > Ni-Mn > Cu-Co > Pb > Fe.     

Geochemical variations of major and trace elements in recent sediments,off the Gulf of Mannar,the southeast coast of India

The Gulf of Mannar along the Tuticorin coast is a coral base of the southeast coast of India. To obtain a preliminary view of its environmental conditions, geochemical distribution of major elements (Si, Al, Fe, Ca, Mg, Na, K, P), trace elements (Mn, Cr, Cu, Ni, Co, Pb, Zn, Cd) and acid leachable elements (Fe, Mn, Cr, Cu, Ni, Co, Pb, Zn, Cd) were analyzed in surface sediment samples from two seasons. Geochemical fractionation confirmed the lithogenic origin of metals, which were mainly associated with the detrital phase. The sediments in the gulf are sandy with abundant calcareous debris, which controls the distribution of total and acid leachable elements. Enrichment factors relative to crust vary by a magnitude of two to three and the presence of trace metals indicates the input of Cr, Pb, Cd, Cu and Zn in both forms through industrial activities. Factor analysis supports the above observation with higher loadings on acid leachable elements and its association with CaCO₃. The increase in concentration of trace metals (Cr, Pb, Cd, Cu, Co, Ni, Zn) along the Gulf of Mannar indicates that the area has been contaminated by the input from riverine sources and the industries nearby. The present study indicates that other sources should be evaluated in the long-term monitoring program.     

Geochemical dispersion of gold related to copper-gold mineralization in northeastern Thailand

The nature of gold dispersion in soils and stream sediments associated with a copper-gold-mineralized system in northeastern Thailand has been investigated as a basis for identifying appropriate geochemical exploration techniques for the search for comparable deposits in similar environments.Soils were collected with varying relationships to mineralization as a basis for determining sample representativity, size distribution of gold, variation with soil horizon and possible pathfinder elements. Similarly, stream sediments were collected to estimate sample representativity, size distribution of gold, variation of gold with depth in the stream sediment profile and to compare the relative recoveries of gold in field-panned and laboratory-prepared heavy-mineral concentrates. Samples were analyzed for Au and potential indicator elements by a variety of methods but mostly by instrumental neutron activation analysis.Results indicate the consistent distribution of fine-grained gold in soils which allows Au analysis of relatively small samples from B-horizon soils to be used effectively and reliably to identify the surficial patterns of gold mineralization in the study area. Anomalous patterns of other indicator elements, Co, As, Cu, Sb, W, Pb, Zn, Ag, Fe and Mn, may contribute additional information regarding type of mineralization. This finding indicates the effectiveness of soil surveys in gold exploration, particularly in areas of deep weathering where fresh bedrock exposures are infrequent.Unlike soils, size distributions of gold in stream sediments, as a result of the local flow regime, vary both between sampling sites and at depths within a sampling site. Exploration requires Au analysis of the fine fraction (minus 63 μm) of active stream sediments to reduce the problem of sampling representativity. The presence of coarse-grained gold in the stream channel has drawn attention to the possible benefit of using the conventional field-panning method as a semiquantitative technique for providing immediate results. However, highly erratic distribution of pannable gold on a very local scale together with variable proportions of the total gold recovered in field-panned or heavy-mineral concentrates highlights a potentially serious drawback of the method. Combination of analysis of the minus 63 μm fraction and field panning appears warranted to cover the possible existence of gold of a wide size range in stream sediments.The overall results indicate the utility of geochemical exploration techniques in the search for gold mineralization. However, particular care is necessary in the design and implementation of geochemical techniques to ensure maximum reliability of exploration.     

Geochemical fractionation of heavy metals in Chilka Lake (east coast of India)—a tropical coastal lagoon

Chilka lake, the largest coastal lagoon of Asia is one of the most dynamic ecosystems along the Indian coast. Historically the lagoon has undergone a considerable reduction in surface area due, in part, to input from natural processes but mostly due to human activities. The purpose of this investigation is to document the heavy metals' affinity for specific geochemical phases in the recently deposited sediments in the lagoon. Thirty-three samples were collected and analyzed for different geochemical phases of Fe, Mn, Cu, Cr, Ni, Pb, and Zn utilizing a sequential extraction scheme. In the nonlithogenous fraction, the exchangeable fraction was not geochemically significant, having <2% of the total metal concentration for all the elements. However, the carbonate fraction contained the following percentages of the total concentration: <1% Fe, 13% Mn, 6% Cu, 4% Cr, 8% Ni, 13% Pb, and 12% Zn, suggesting the detrital origin of the sediments. Reducible and organic matter-bound fractions were the significant phases in the nonlithogenous fraction, containing 9% Fe, 16% Mn, 15% Cu, 16% Cr, 16% Ni, 14% Pb, and 14% Zn in the former and 4% Fe, 3% Mn, 17% Cu, 3% Cr, 14% Ni, 15% Pb, and 14% Zn in the latter. The phenomenon has been attributed to the scavenging affinity of Fe-Mn oxides and affinity for sorption into organic matter of the lagoon sediments. The lithogenous, residual fraction generally considered as a guide for natural background values was determined to contain 87% Fe, 67% Mn, 61% Cu, 77% Cr, 61.3% Ni, 56% Pb, and 60% Zn of the total concentrations.     

Stream water, an ideal medium for rapidly locating polymetallic mineralization in forest-swamp terrain: a case study in the Da Hinggan Mts., northern Heilongjiang, China

A forest-bog landscape is developed in an area of moderate to low topography in northeastern China. Bogs are widespread along U- and V-shaped valleys (200–2000 m wide) and in depressions. Due to the cold climate, it was initially thought that chemical weathering would be slight in the area. However, a study of the geochemistry of surface water showed that, although most elements occur in relatively low concentrations compared to average contents in world river water, a number of mobile elements are dispersed over long distances. Marked Cu, Zn, Fe, Mn, and SO²⁻₄ anomalies, and relatively weak Ni, Co, Be, Pb and F anomalies form in stream water in the vicinity of known mineralization. Concentrations of Cu, Pb, Zn, Fe, and Mn in suspensates show no marked variations between background and anomalous streams whereas Ag exhibits a marked increase in suspensates near the mineralization. The pH of stream water near the mineralization is considerably lower than the 5 to 6.5 values recorded for background water. It can be concluded that water plays an important role in transporting elements chemically and stream water is a useful medium to sample in follow-up geochemical surveys for base and precious metals (Ag) in this landscape.     

Spatial distribution and geochemical baselines of major/trace elements in soils of Medak district,Andhra Pradesh,India

Regional-scale variations in soil geochemistry were investigated with special reference to differences among soil groups and lithology in an area of 9,699 km² in Medak district, Andhra Pradesh, India. The concentrations of 29 elements (major: Si, Al, Fe, Mn, Mg, Ca, Na, K, Ti, P and trace: As, Ba, Cd, Co, Cr, Cu, F, Mo, Ni, Pb, Rb, Se, Sr, Th, U, V, Y, Zn, Zr) in 878 soil samples collected (557-topsoil, 321-subsoil) at a sampling density of 1 site/17 km² from 557 sites representative of all the soil types present in studied area were determined, and their elemental composition are discussed. The baseline levels of these elements in soils are determined over different lithological units for the identification of anomalous values relative to these. For the first time, geochemical maps for Medak district are prepared on 1:50,000 scale and the lithogeochemical database generated provides information on the lateral and vertical distribution of elements in soil. The spatial variations in the distribution of elements reflect underlying geologic characteristics. Box-plots reveal that the concentration of most of the elements in soils were not strongly dependent on the soil group but the soil-geochemistry abruptly changes with the change in the soil parent materials indicating that the distribution of elements is mostly influenced by the bedrock lithology and other natural processes acting on them. For instance, the concentrations of Co, Cu, Fe, Mn, Ti, V and Zn are high in soils developed on basaltic terrain while the soils developed on granitic and gneissic terrain exhibit high elemental concentrations of K, Pb, Rb, Si, Th and Y. Alfisols had relatively high contents of elements while entisols had lower concentrations of most of the elements. The database can be used in the chemical characterisation of different geological units as well as applications in various environmental and agricultural fields. The results indicate that regional geology is an important determinant of soil geochemical baselines for soil pollution assessment and further emphasizes the importance of determining background levels locally. The defined baselines can be used to establish background values for future soil surveys.     

Biogeochemical evolution of trace elements in a pristine watershed in the Brazilian southeastern coastal region

Establishing ‘reference sites’ is a difficult task and a critical factor in determining the baseline functioning of ecosystems. The information thus obtained on nutrient and contaminant background concentrations in turn subsidizes the remediation of impacted landscapes. This paper reports a study on metal (Cr, Cu, Pb, Zn, Mn, Fe and Al) and nutrient (C) distribution in sediments from Capivari River watershed (Praia do Sul Biological Reserve, Ilha Grande, Rio de Janeiro State, Brazil), an area where typical SE Brazilian coastal ecosystems are located. Contrary to what one would expect from the high rate at which these ecosystems have been deteriorating in recent decades, the study site is surprisingly well preserved. The present study was developed to assess variations in heavy metal concentrations in river basin sediments, to identify the geochemical carriers of these elements, and determine the influence of water quality and organic matter on their distribution. Results showed that heavy metal distribution has been influenced by the natural biogeochemical properties of those ecosystems found in an upland-to-lowland sequence in the watershed. Minimum and maximum total concentration were: 5 and 23 mg/kg for Cr; 4 and 29 mg/kg for Cu; 13 and 53 mg/kg for Pb; 24 and 142 mg/kg for Zn; 54 and 342 mg/kg for Mn; 0.8 and 7.2% for Fe; 0.5 and 4.9% for Al; 6.3 and 25% for C. The pH and E_H are the key-parameters in explaining total metal concentration decrease in the swamp area, where dissolution processes and losses through metal transport seem important. The most important geochemical carriers are Al in the basin’s “continental” stretch and Fe in the estuarine portion. The data also provide evidence showing that organic matter is the key-parameter in Cu concentration control in the sediments through burial and accumulation processes especially in the swamp area. Heavy metal concentrations in sediments from the study area are generally lower than those found in similar regional ecosystems. Surface enrichment in heavy metal concentrations in collected sediment cores was not observed. The authors therefore conclude that this site is suitable as a ‘reference site’ for studies on the biogeochemistry and ecotoxicology of SE Brazilian coastal ecosystems.     

Regional geochemical baseline concentration of potentially toxic trace metals in the mineralized Lom Basin,East Cameroon: a tool for contamination assessment

The distribution of trace metals in active stream sediments from the mineralized Lom Basin has been evaluated. Fifty-five bottom sediments were collected and the mineralogical composition of six pulverized samples determined by XRD. The fine fraction (<?150 µm) was subjected to total digestion (HClO₄?+?HF?+?HCl) and analyzed for trace metals using a combination of ICP-MS and AAS analytical methods. Results show that the mineralogy of stream sediments is dominated by quartz (39–86%), phyllosilicates (0–45%) and feldspars (0–27%). Mean concentrations of the analyzed metals are low (e.g. As?=?99.40 µg/kg, Zn?=?573.24 µg/kg, V?=?963.14 µg/kg and Cr?=?763.93 µg/kg). Iron and Mn have significant average concentrations of 28.325 and 442 mg/kg, respectively. Background and threshold values of the trace metals were computed statistically to determine geochemical anomalies of geologic or anthropogenic origin, particularly mining activity. Factor analysis, applied on normalized data, identified three associations: Ni–Cr–V–Co–As–Se–pH, Cu–Zn–Hg–Pb–Cd–Sc and Fe–Mn. The first association is controlled by source geology and the neutral pH, the second by sulphide mineralization and the last by chemical weathering of ferromagnesian minerals. Spatial analysis reveals similar distribution trends for Co–Cr–V–Ni and Cu–Zn–Pb–Sc reflecting the lithology and sulphide mineralization in the basin. Relatively high levels of As were concordant with reported gold occurrences in the area while Fe and Mn distribution are consistent with their source from the Fe-bearing metamorphic rocks. These findings provide baseline geochemical values for common and parallel geological domains in the eastern region of Cameroon. Although this study shows that the stream sediments are not polluted, the evaluation of metal composition in environmental samples from abandoned and active mine sites for comparison and environmental health risk assessment is highly recommended.     

Geochemical and equilibrium trends in mine pit lakes

Chemical composition and equilibrium trends in mine pit lakes were examined to provide guidance for the application of geochemical models in predicting future lake water quality at prospective open pit mines. Composition trends show that elevated solute levels generally occur only at the extremes of acidic and alkaline pH conditions. Concentrations of cationic metals (Al, Cd, Cu, Fe, Mn, Pb, and Zn) are elevated only in acidic pit lakes, whereas anionic metalloids (As and Se) are generally elevated only in alkaline pit lakes. These trends are indicative of sulfide mineral oxidation and evapoconcentration for acidic and alkaline conditions, respectively.For nearly all pit lakes, SO₄ is the dominant solute, but is limited by gypsum solubility. Fluorite, calcite, and barite are also important solubility controls. Well-defined solubility controls exist for the major metals (Al, Fe, Mn), including jurbanite and alunite for Al, ferrihydrite for Fe, and manganite, birnessite, and, possibly, rhodochrosite for Mn. Determinations of definite controls for the minor metals are less distinct, but may include otavite for Cd, brochantite and malachite for Cu, cerrusite and pyromorphite for Pb, and hydrozincite and Zn silicates for Zn. Concentrations of As and Se appear to be limited only by adsorption, but this control is sharply diminished by increased pH and SO₄ concentration. In general, the concentrations of minor metals in pit lakes are not well represented by the theoretical solubilities of pure-phase minerals contained in the thermodynamic databases. Hence, modeling efforts will generally have to rely on empirical data on the leaching characteristics of pit wall-rocks to predict the concentrations of minor metals (Cd, Cu, Pb, Zn) in mine pit lakes.Methodologies for predicting pit lake water chemistry are still evolving. Geochemical and equilibrium trends in existing pit lakes can provide valuable information for guiding the development and application of predictive models. However, mineralogical studies of pit lake sediments, suspended particles, and alteration assemblages and studies of redox transformations are still needed to validate and refine the representations of geochemical processes in water quality models of mine pit lakes.     

Transport and sediment–water partitioning of trace metals in acid mine drainage: an example from the abandoned Kwangyang Au–Ag mine area, South Korea

Transport and sediment–water partitioning of trace metals (Cr, Co, Fe, Pb, Cu, Ni, Zn, Cd) in acid mine drainage were studied in two creeks in the Kwangyang Au–Ag mine area, southern part of Korea. Chemical analysis of stream waters and the weak acid (0.1 N HCl) extraction, strong acid (HF–HNO₃–HClO₄) extraction, and sequential extraction of stream sediments were performed. Heavy metal pollution of sediments was higher in Chonam-ri creek than in Sagok-ri creek, because there is a larger source of base metal sulfides in the ores and waste dump upstream of Chonam-ri creek. The sediment–water distribution coefficients (K _d) for metals in both creeks were dependent on the water pH and decreased in the order Pb ≈ Al > Cu > Mn > Zn > Co > Ni ≈ Cd. K _d values for Al, Cu and Zn were very sensitive to changes in pH. The results of sequential extraction indicated that among non-residual fractions, Fe–Mn oxides are most important for retaining trace metals in the sediments. Therefore, the precipitation of Fe(–Mn) oxides due to pH increase in downstream sites plays an important role in regulating the concentrations of dissolved trace metals in both creeks. For Al, Co, Cu, Mn, Pb and Zn, the metal concentrations determined by 0.1 N HCl extraction (Korean Standard Method for Soil Pollution) were almost identical to the cumulative concentrations determined for the first three weakly-bound fractions (exchangeable + bound to carbonates + bound to Fe–Mn oxides) in the sequential extraction procedure. This suggests that 0.1 N HCl extraction can be effectively used to assess the environmentally available and/or bioavailable forms of trace metals in natural stream sediments.     

A national-scale geochemical and mineralogical survey of soils of the conterminous United States

In 2007, the US Geological Survey initiated a low-density (1 site per 1600 km², c. 4800 sites) geochemical and mineralogical survey of soils of the conterminous USA. The ideal sampling protocol at each site includes a sample from 0–5 cm depth, a composite of the soil A horizon, and a sample from the soil C horizon. The <2-mm fraction of each sample is analyzed for Al, Ca, Fe, K, Mg, Na, S, Ti, Ag, Ba, Be, Bi, Cd, Ce, Co, Cr, Cs, Cu, Ga, In, La, Li, Mn, Mo, Nb, Ni, P, Pb, Rb, Sb, Sc, Sn, Sr, Te, Th, Tl, U, V, W, Y and Zn by inductively coupled plasma-mass spectrometry and inductively coupled plasma-atomic emission spectrometry following a near-total digestion in a mixture of HCl, HNO₃, HClO₄ and HF. Separate methods are used for As, Hg, Se and total C on this same size fraction. The major mineralogical components are determined by a quantitative X-ray diffraction method. Sampling was completed in 2010 with chemical and mineralogical analysis currently underway. Preliminary results for a swath from the central USA to Florida clearly show the effects of soil parent material and climate on the chemical and mineralogical composition of soils. A sample archive will be established and made available for future investigations.     

Heavy metal distribution and assessment in stream sediments of River Orle,Southwestern Nigeria

Ten heavy metals, namely, Ag, As, Cd, Co, Cr, Cu, Hg, Ni, Pb and Zn were partially extracted using aqua regia digestion method and analysed by ICP-AES from 56 stream sediment samples collected from River Orle, Igarra area, southwestern Nigeria. The analytical results were used to produce geochemical distribution maps for the elements and were subjected to univariate statistical analysis in order to evaluate the distribution and abundance of the heavy metals in the study area. The degree of pollution of these stream sediments by these heavy metals was evaluated by calculating such parameters as enrichment factors (EF), as well as pollution load and geo-accumulation indices (PLI and Igeo). Co, Cr, Cu, Ni, Pb and Zn are widely distributed in the drainage system while the distribution of Ag, Cd, As and Hg is restricted to only parts of the drainage system with Ag and Cd being localized to one sample site each near Epkeshi in the southern part of the study area. Cr and Pb display anomalously high concentrations, each from a site, also in the same locality where Ag and Cd were detected, indicating the likelihood that the four elements, Cr, Pb, Ag and Cd, are genetically related. Calculation of the enrichment factor (EF), pollution load index (PLI) and geo-accumulation index (Igeo) yielded results that indicate that all the 56 stream sediment sites, except one located about 4 km southeast of Epkeshi in the southern part of the Orle drainage system, are practically unpolluted by heavy metals. The relatively high metal concentration of this anomalous site having Pb EF of 62.5, PLI of 1.14 and Pb Igeo of 2.44 signifies Pb pollution. Both natural and anthropogenic sources of the Pb contamination around Epkeshi locality are possible. In conclusion, the levels of concentrations of heavy metals in the study area, in general, do not constitute any serious environmental risk except for Pb which needs to be monitored at only one site in the study area. Therefore the concentration ranges for the different heavy metals in the study area can serve as baseline environmental data against which the degree of pollution of these heavy metals can be evaluated in future.