Geochemical Atlas of Slovakia and examples of its applications to environmental problems

Results of comprehensive geochemical mapping and thematic studies of the Slovak territory (rocks, soils, stream sediments, groundwaters, biomass, and radioactivity) in the first half of the 1990s led to several new research programmes in Slovakia, within the frame of which new methodologies for geochemical data evaluation and map visualization were elaborated. This study describes the application and elaboration of data from the Geochemical Atlas of the Slovak Republic at national and regional levels. Based on the index of environmental risk (I_ER = ΣPEC/PNEC), the level of contamination for the geological component of the environment in Slovakia was evaluated. Approximately 10.5% of Slovakia’s territory was characterized as being environmentally disturbed to highly disturbed. In the areas where environmental loadings have accumulated, 14 regions where environmental risks existed due to high element concentrations were defined. The model calculations of health risk estimates based on the databases of the Geochemical Atlas for groundwater and soils indicate that the possible risk occurrence of carcinogenic diseases from groundwater arsenic contents is high in more than 10% of Slovakia, whereas the chronic risk is negligible. To determinate the background and threshold levels a combined statistical–geochemical approach was developed and applied as an example for groundwater at the national level as well as for single groundwater bodies. The results of statistical method application for the whole groundwater body (GBW) were compared with the background values for anthropogenically non-influenced areas in GBW. Final background value took into account time variations and spatial distribution of the element in GBW. Furthermore, based on the database from the Geochemical Atlas for groundwater, groundwater bodies potentially at qualitative risk were delineated for the whole of Slovakia. From a total of 101 groundwater bodies 17 were characterized as being at risk and 22 as being at possible risk.     

Application of health risk assessment method for geological environment at national and regional scales

Health risk, defined as possibility or probability of health damage, illness or death of humans due to exposure to risk factors in the environment, was derived for geological environment (soils) and estimated at national scale for the whole Europe and at more detailed regional scale for Slovak Republic. The assessment was based on data obtained from international geochemical mapping of Europe (Geochemical Atlas of the Europe—827 soil samples) and national geochemical mapping programme of the Slovak Republic (9,860 soil samples). The following chemical elements were evaluated: As, B, Ba, Be, Cd, Cu, F, Hg, Mn, Mo, Ni, Pb, Sb, Se and Zn. The health risk assessment method was based on calculations of average daily doses of individual elements analysed in every collected soil sample. Exposure levels were set by using exposure parameters and reference doses from integrated databases of US EPA. The results of calculations were transformed into various sorts of maps (dot, pixel) to delineate areas where increased contents of risk elements can pose risk to human health. The average levels of chronic and carcinogenic risk are presented in the form of tables for single European countries and administrative units of Slovak republic. The results of European mapping (Geochemical Atlas of Europe) indicate that increased levels of potentially toxic elements in soil (mainly As, Pb and Ni) occur primarily in the countries of southern and western Europe. Such elements are associated with increased health risk for resident population. For the countries of northern Europe health risk was estimated at significantly lower level. Relatively high sampling density in Slovak Republic made it possible to calculate health risk at more detailed scale for individual administrative units (municipalities, provinces). The increased health risk level was found in areas well known for high soil contamination (e.g. mining areas).     

Geochemical mapping in northern Honshu,Japan

Geochemical mapping of northern Honshu in the Northeast Japan Arc was carried out using stream sediments at a sampling density of one sample per 130 km². More than 50 elements were determined in 395 stream sediment samples (<0.18 mm fraction). In geochemical maps, areas with especially low concentrations of large ion lithophile elements (LILE), Be and Li widely overlap with the distribution of Quaternary volcanic rocks along the volcanic front. The areas rich in mafic elements are associated with mafic rocks in many cases. On a regional scale, Ni, Cr and Cu contents are higher in the eastern Paleozoic–Mesozoic basement zone, Pb and Tl tend to be higher on the western zones, and Zn and Cd are high in the western back-arc zone. The areas especially rich in Cu, Zn, Cd, Pb, Bi and Tl coincide with the distribution of large mineral deposits. High concentrations related to Kuroko, hydrothermal-vein, and skarn-type deposits are recognized. High values of As and Sb are related to active geothermal areas near volcanoes and ore deposits. Chemical variations of K, Ce, Th and Sn in the stream sediments are concordant with chemical variations in major rocks. The median and mean concentrations for the stream sediments in northern Honshu, showing arc signatures, are lower in Rb, Cs, Th, Li, K, Be, Ta, LREE, Ni, Hg and Sn, and higher in Sc, Ca and Cd relative to the whole area of Japan, largely because of the contribution of Cenozoic island-arc volcanic rocks that are generally poor in incompatible elements. The averaged chemical compositions of the stream sediments for the geologic zones show systematic variations of many elements. The contrasting variations of LREE and Th contents, which are lower in the zones of Cenozoic rocks relative to the zones of pre-Neogene basements, reflect the regional variations in the main rocks, and also reflect the change of geological settings of the studied area from the continental margin to an island arc during the Cenozoic.     

Elemental Concentrations of Stream Sediments in Southern China

Over 3 million samples were collected from southern China at a density of 1–2 stream sediment samples per square kilometre as part of the Regional Geochemistry National Reconnaissance (RGNR) programme of China initiated in the late 1970s. Approximately 5244 composite samples of stream sediments from twelve provinces of southern China were prepared from the original RGNR samples collected from a territory with an area of 2300000 km² at a density of one composite sample per 1:50000 map sheet (about 400 km²). Seventy‐six elements were determined by the geoanalysis laboratory of Henan Province (platinum‐group elements) and by the Institute of Geophysical and Geochemical Exploration (IGGE) laboratory for the remainder. Internal quality and external quality control methods were applied to ensure that the analytical data were comparable. Statistics were used to derive the mean and background values and indicate the average concentrations of the seventy‐six elements. Comparisons were made against the mean values obtained from stream sediments, floodplain sediments, overall sediments and overall soils of the entire territory of China. The concentrations of Hg, Cd, rare earth elements and 24 other elements were higher than their background for the whole of China. In contrast, the concentration of Na₂O, CaO, Ba and Sr were lower in the stream sediments in southern China than their whole China background.     

Hydrochemical and isotopic characteristics of groundwater in the Souss Upstream Basin, southwestern Morocco

Heterogeneous shallow Plio-Quaternary formations of the Souss Plain represent the most important aquifer in southern High Atlas Mountains in Morocco. The present work was conducted in the Souss Upstream Basin to identify the chemical characteristics and the origin of groundwater in an aquifer under semi-arid climate. Isotopic and hydrochemical compositions combined with geological and hydrogeological data were used for this purpose. The total dissolved solids vary from 239 to 997 mg l⁻¹, and the following groundwater types are recognized: Ca²⁺–Mg²⁺–HCO₃⁻, Ca²⁺–Mg²⁺–SO₄²⁻ and Ca²⁺–Mg²⁺–Cl⁻. The groundwater is saturated and slightly supersaturated with respect to carbonate minerals and undersaturated with respect to evaporite minerals, which means that the groundwater composition is largely controlled by the dissolution of carbonate rocks known in the basin. The isotopic contents of groundwaters ranged from −8‰ to −5.2‰ for δ¹⁸O, from −52‰ to −34‰ for δD, and from 0 to 5.5 TU for tritium. The hydrogen (δD) and oxygen (δ¹⁸O) isotope signatures reveal a significant infiltration before evaporation takes place, indicating a major recharge directly from fractures in the crystalline and limestone formations of Atlas Mountains (above 800 m a.s.l.) and infiltration of surface water in the alluvial cones at the border of the Atlas basins. The very low tritium values suggest that the groundwater recharge follows a long flow path and a mixing between old and modern water is shown. However, a slight evaporation effect is noted in the southern part of the basin close to the Anti-Atlas Mountains.     

Changes in groundwater chemistry due to metallurgical activities in an alluvial aquifer in the Moa area (Cuba)

The aim of this work is to evaluate the changes in groundwater chemistry in an alluvial aquifer in the Moa area. Surface and ground water, metallurgical waste and various geological material samples were collected in order to evaluate groundwater composition. The results show that the alluvial aquifer is polluted with SO₄^2-, Mg²⁺and heavy metals. According to its major components in the alluvial aquifer, two types of groundwater are identified: magnesi-bicarbonated and sulphate-magnesic. Maximum SO₄^2– and Mg²⁺ contents are more than 1000 mg/L, and are four times higher than the acceptable levels for human consumption of water. The high values of Cr(VI), Ni(II), Mn(II) Fe_(total), SO₄^2– and Mg²⁺ in alluvial aquifers are due to polluted recharge from metallurgical waste from the tailing dam. This recharge is favoured by the preferential flow due to desiccation cracks in metallurgical waste. Geochemical modelling showed that potentially toxic heavy metals might exist largely in the forms of MSO₄^2– and M²⁺ in pore water of SAL metallurgical waste. All samples were supersaturated in goethite and hematite. Results from batch testing indicate that the heavy metals have two origins: natural, due to the existing ultramaphic rocks and laterites, and anthropogenic, by metallurgical waste rich in sulphate and (oxy)hydroxide minerals. These results highlight the need to locate and evaluate a new water source to supply the population of the city of Moa.     

Low-density geochemical mapping in Hungary

Guidelines for a low-density geochemical survey were described in 1990 by the Western European Geological Surveys. A low-density geochemical survey of Hungary was carried out in 1991–1995. The results are useful for future surveys and for the IGCP 360 project ‘Global Geochemical Baseline’. In regions with well-developed drainage systems in Hungary, 196 catchment basins of approx. 400 km² were delineated and flood-plain deposits sampled at their outlets. The samples were taken from 0 to 10 cm and from 50 to 60 cm depths. Samples were analysed by ICP-AES and AAS techniques in two laboratories. A Geochemical Atlas of Hungary is in preparation that will show the distribution of 25 elements in the two sampled layers. Maps for the lower layer represent regional geochemical baseline values and a geochemical subdivision of the country (maps showing the distribution of element associations) was made on the basis of factor variables. Maps constructed from the data of the upper sampling level show us the present state of contamination of the surface. The results of this survey have contributed to the establishment of guidance values for soils prepared by the Hungarian Ministry of the Environment in 1995. Safe levels were established for As, Cd, Cr, Cu, Hg, Pb and Zn and regional environmental loads plotted. Differences between the median values of the two levels are generally small. However, the concentrations of certain elements like P, Pb and S are significantly greater in the upper layer reflecting contamination from agriculture. In certain regions, the rate of sedimentation was fairly fast such that the environmental effects of ore mining in Transylvania and southern Slovakia as well as those of heavy industry in northern Hungary can be observed in samples from the lower level. The main factor controlling the geochemical pattern in Hungary is the predominance of young (Pleistocene or Miocene) clastic sediments at the surface. Approx. 90% of the surface is covered by these young sediments. This kind of survey has the disadvantage of not providing enough contrast to differentiate geologically dissimilar areas but it has the advantage to provide regional surface background geochemical data and it helps to outline areas of possible surface contamination. Based on the results of this survey we conclude that it would be much better to sample smaller, but geologically homogeneous areas in mountainous terrain to obtain data characteristic of the geochemical background of lithologic units. This approach would mean a sampling density of a few tens of km²/sample for hilly areas, and a few hundred km²/sample for lowland areas.     

Geological and geochemical examination of arsenic contamination in groundwater in the Holocene Terai Basin, Nepal

Geological and geochemical study has been carried out to investigate arsenic contamination in groundwater in Nawalparasi, the western Terai district of Nepal. The work carried out includes analyses of core sediments, provenance study by rare earth elements analyses, ¹⁴C dating, and water analyses. Results showed that distribution of the major and trace elements are not homogeneous in different grain size sediments. Geochemical characteristics and sediment assemblages of the arsenic contaminated (Nawalparasi) and uncontaminated (Bhairahawa) area have been compared. Geochemical compositions of sediments from both the areas are similar; however, water chemistry and sedimentary facies vary significantly. Extraction test of sediment samples showed significant leaching of arsenic and iron. Chemical reduction and contribution from organic matter could be a plausible explanation for the arsenic release in groundwater from the Terai sediments.     

Cation exchange processes and human activities in unconfined aquifers

During the 1999–2002 water years, a hydrogeological research project was carried out on the unconfined aquifer of Trifilia in the Peloponnese. Seawater intrusion due to overpumping, and intensive use of fertilizers caused the groundwater quality degradation that is a typical case for the coastal aquifers in Greece. Isopiezometric maps along with ion distribution balances, ion distribution maps and factor analysis indicate the existence of three zones of groundwater quality. In the first zone of saline water, a cation exchange process between the Ca²⁺ of sediments and the Na⁺ of groundwater contribute to the formation of the water type Na⁺-Ca²⁺-Cl^–. In the second zone, which is considered as a transition zone, dominate the Ca²⁺-Na⁺-HCO₃^–-Cl^– water type. In the third zone of Ca²⁺-HCO₃^–-SO₄^2– water type, relationships among Ca²⁺, SO₄^2–, NO₃^– and NH₄ can be attributed to the dissociation of ammonium nitrate and sulfate fertilizers on one hand, and Ca²⁺ derivation from cation exchange processes between water, rocks and clay minerals, such as smectite and illite, on the other.     

滇黔桂卡林型金矿区水系沉积物和岩石金含量与时空分布

为研究滇黔桂卡林型金矿区水系沉积物和岩石中金的地球化学时空分布及其与金矿规模的对应关系,系统收集了该区1:20万区域化探全国扫面计划水系沉积物和全国地球化学基准计划岩石金的地球化学数据,绘制了水系沉积物和岩石金的地球化学分布图。滇黔桂卡林型金矿区以水系沉积物金地球化学异常面积大于1000 km^2为准,共圈定5处金的地球化学省,这些金的地球化学省同时也是矿床大规模产出的部位。区内右江盆地水系沉积物金背景值(1.94×10^–9)高于扬子克拉通(1.68×10^9),其内以泥岩、页岩、砂岩、灰岩为代表的容矿岩石金背景值(0.51×10^–9)也高于扬子克拉通(0.39×10^–9)。研究区不同构造单元及沉积相中水系沉积物金背景值受岩石金背景值的制约。金的地球化学省是地壳演化过程中不均匀分布的高金背景岩石、金矿化作用及金矿床次生风化作用相互叠加的结果。该研究有助于有效判断异常成因、识别成矿作用存在,对研究金的区域成矿规律和聚焦找矿靶区具有重要意义。     

Application of multi-element statistical analysis for regional geochemical mapping in Central Japan

Some 434 stream sediment samples were collected in Central Japan for a nationwide geochemical mapping project. The resulting geochemical maps are compared with geological, mineral resource and land use maps. Spatial distribution patterns of elemental concentrations in stream sediments are determined mainly by surface geology. Elevated elemental concentrations of alkali elements, Be, Ga, Y, Cs, Ba, lanthanide (Ln), Tl, Th, and U are consistent with outcrop areas of granite, felsic volcanic rock, and accretionary complexes. High concentrations of MgO, Al₂O₃, P₂O₅, CaO, 3d transition metals, Zn, and Sr are present in sediments supplied from mafic volcanic rock, high pressure metamorphic rocks, and mafic-ultramafic rocks in accretionary complexes.A procedure is established and guidelines are set for a statistical test suite for geochemical mapping. Analysis of variance (ANOVA) and multiple comparison tests are effective for comparing means among the data subsets that are classified by parent lithological materials. Among the many procedures that have been proposed for multiple comparison tests, the Holm procedure was selected for this study. Multiple comparison statistically confirmed the correspondence of elemental abundance in stream sediments with surface geologies. However, visual interpretation of some elements is inconsistent with results of multiple comparison. According to the Holm procedure, the U content in stream sediments is affected not by granite, but by felsic volcanic rock. The Holm procedure clarifies that As, Sb, and Bi, that are not explained by the presence of mineral deposits, are enriched significantly in samples derived from accretionary complexes. Hydrothermal activity on the ocean floor might affect their levels of enrichment. Significant enrichment of Cu, Zn, Cd, Sn, Sb, Hg, and Pb observed in urban areas are also supported by the Holm procedure. The authors inferred that these sediment samples had been contaminated.     

Contamination of water and soil by the Erdenet copper–molybdenum mine in Mongolia

As one of the largest copper–molybdenum (Cu–Mo) mines in the world, the Erdenet Mine in Mongolia has been active since 1978 and is expected to continue operations for at least another 30 years. In this study, the potential impacts of mining activities on the soil and water environments have been evaluated. Water samples showed high concentrations of sulfate, calcium, magnesium, Mo, and arsenic, and high pH values in the order of high to low as follows: tailing water > Khangal River > groundwater. Statistical analysis and the δ²H and δ¹⁸O values of water samples indicate that the tailing water directly affects the stream water and indirectly affects groundwater through recharge processes. Soil and stream sediments are highly contaminated with Cu and Mo, which are major elements of ore minerals. Based on the contamination factor (CF), the pollution load index (PLI), and the degree of contamination (C_d), soil appears to be less contaminated than stream sediments. The soil particle size is similar to that of tailing materials, but stream sediments have much coarser particles, implying that the materials have different origins. Contamination levels in stream sediments display a tendency to decrease with distance from the mine, but no such changes are found in soil. Consequently, soil contamination by metals is attributable to wind-blown dusts from the tailing materials, and stream sediment contamination is caused by discharges from uncontained subgrade ore stock materials. Considering the evident impact on the soil and water environment, and the human health risk from the Erdenet Mine, measures to mitigate its environmental impact should be taken immediately including source control, the establishment of a systematic and continuous monitoring system, and a comprehensive risk assessment.     

The source of fluoride toxicity in Muteh area,Isfahan, Iran

Endemic dental fluorosis has been observed in most inhabitants of three villages of Muteh area, located in northwest of Isfahan province, with mottled enamel related to high levels of fluoride in drinking water (1.8–2.2 ppm). Forty-seven groundwater samples from six villages were collected and fluoride concentrations along with physico-chemical parameters were analyzed. Fluoride concentration in this area varies from 0.2 to 9.2 mg/l with highest fluoride level at Muteh gold mine (Chahkhatun mine). Fluoride concentration positively correlates with pH and HCO₃ ⁻ indicating that alkaline pH provides a suitable condition for leaching of fluoride from surrounding rocks. The district is mainly covered by three lithological units, namely, metamorphic and granite rocks, alluvial sediments, and carbonate rocks. Factor analysis shows that parameters can be classified into four components: electrical conductivity (EC), total dissolved solids (TDS), Cl⁻, Na⁺ and K⁺, pH and F⁻, SO₄ ²⁻and Mg²⁺, HCO₃ ⁻ and Ca₂ ⁺. The groundwaters from the three geological units were compared using Mann–Whitney U test. The order of median fluoride concentration is: metamorphic and granite rocks > alluvial sediments > carbonate rocks. Hence, the fluoride content is most probably related to fluoride-bearing minerals such as amphibole and mica group minerals in metamorphic and granitic rocks. The concentration of fluoride in drinking water wells located near the metamorphic complex in Muteh area is above 2 ppm.     

Influence of surface geology and mineral deposits on the spatial distributions of elemental concentrations in the stream sediments of Hokkaido,Japan

An elucidation of the background levels of heavy metals, including certain toxic elements, is very essential to accomplish an important environmental assessment. A regional geochemical mapping in Hokkaido, Japan was undertaken by the Geological Survey of Japan, AIST as part of a nationwide geochemical mapping for this purpose. There were 692 stream sediments collected from the active channel (1 sample) / (100 km²) in Hokkaido and the fine fraction sieved through a 180 μm screen was analyzed using the AAS, ICP-AES, and ICP-MS techniques. The regional geochemical maps for 51 elements were created as a 2000 m mesh map using the geographic information system software. Spatial distribution patterns of elemental concentrations in stream sediments, particularly Neogene–Quaternary volcanic and pyroclastic rocks, are primarily determined by surface geology. The correspondence of elemental concentrations in stream sediments to parent lithology is clearly indicated by ANOVA and a multiple comparison. Sediment samples supplied from mafic volcanic and felsic–mafic pyroclastic rocks are significantly rich in MgO, Al₂O₃, P₂O₅, CaO, Sc, TiO₂, V, MnO, Total (T)-Fe₂O₃, Co, Zn, Sr, and heavy rare earth elements (REEs) (Y and Eu–Lu), but significantly lacking in alkali elements, Be, Nb, light REEs (La–Nd), Ta, Tl, Th, and U. Accretionary complexes with sedimentary rocks derived from sediments are in stark contrast to volcanic and pyroclastic rocks. Accretionary complexes with mafic–ultramafic rock have significantly elevated Nb, Ta, and Th abundances in sediments besides MgO, Cr, Ni, Co, and Cu. This inexplicable result is caused by the mixed distributions of granite and ultramafic–mafic rocks.The watersheds with mineral deposits relate to the high concentrations of certain elements such as Zn, As, and Hg. The geochemically anomalous pattern, which is a map of the regional anomalies, and a scatter diagram were applied to examine the contribution of mineral deposits to MnO, T-Fe₂O₃, Cr, Cu, Zn, As, Cd, Sb, Hg, Pb, and Bi concentrations. Consequently, they were grouped into four types: 1) Mineral deposits with no outliers resulting from mineralization (MnO, T-Fe₂O₃, and Cr), 2) sediments supplied from watersheds without metal deposits conceal high metal inputs from known mineral deposits (Cu), 3) deposits from a geochemically anomalous area that closely relates to the presence of mineral deposits (As, Sb, and Hg), and 4) deposits from the widely altered zone associated with the Kuroko as well as hydrothermal deposits corresponding to geochemically anomalous patterns (Zn, Cd, and Pb). This study provides an important regional geochemical database for a young island-arc setting and interpretational problems, such as complicated geology and active erosion, that are unique to Japan.     

Tectonic terranes, metallogeny and regional geochemical surveys: an example from northern British Columbia

This study utilizes three major data sources: distribution of geological units; density, type, age and distribution of mineral deposits; and elemental analyses from regional geochemical stream sediment surveys to define parameters that ‘characterize’ tectonic terranes in northern British Columbia. A similar approach could be applied anywhere in the Canadian Cordillera.This area, NTS map sheets 104N, 104O and 104P along the British Columbia-Yukon border, forms a transect through allochthonous terranes into North American rocks. These are: the allochthonous island-arc Stikine, oceanic Cache Creek, cataclastic Yukon/Tanana, and island-arc Quensel terranes, the pericratonic Dorsey terrane; the parautochthonous oceanic Sylvester allochthon; and the autochthonous miogeoclinal North American Cassiar terrane. Plutonic rocks of Jurassic-Cretaceous to Tertiary age intrude all terranes.Data sources used in the study are geological base maps and reports, the Ministry of Energy Mines and Petroleum Resources' mineral deposit database (MINFILE) and analytical data from the National Regional Geochemical Survey stream sediment and water sampling program.Geological maps were compiled from various sources and plotted to act as bases for geochemical and mineral deposit overlays for analysis and interpretation.Geochemical samples were separated into background and anomalous populations and compared according to their source terranes. We found that mean concentrations from background sample populations for some elements are statistically distinctive for different terranes. Unfortunately, elemental correlation coefficients for the terranes are similar so cannot be used to characterize each terrane.Data on mineral deposits and occurrences were compiled from minfile and other sources. Particular attention was paid to deposits with histories of production or significant reported reserves. Deposits were sorted by type and commodity to produce synoptic metallogenic maps.The combined data from geological, geochemical and mineral deposit databases form a strong tool for interpreting and predicting patterns of mineralization.     

Zn, Pb, Cu and As distribution patterns in overbank and medium-order stream sediment samples: their use in exploration and environmental geochemistry

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.     

Investigation of fluoride contamination and its mobility in groundwater of Simlapal block of Bankura district,West Bengal,India

The occurrence of dental/skeletal fluorosis among the people in the study area provided the motivation to assess the distribution, severity and impact of fluoride contamination in groundwater of Bankura district at Simlapal block, West Bengal, India. To meet the desired objective, groundwater samples were collected from different locations of Laxmisagar, Machatora and Kusumkanali regions of Simlapal block at different depths of tube wells in both pre- and post-monsoon seasons. Geochemical results reveal that the groundwaters are mostly moderate- to hard-water type. Of total groundwater samples, 37% are situated mainly in relatively higher elevated region containing fluoride above 1.5 mg/L, indicating that host aquifers are severely affected by fluoride contamination. Machatora region is highly affected by fluoride contamination with maximum elevated concentration of 12.2 mg/L. Several symptoms of fluorosis among the different age-groups of people in Laxmisagar and Machatora areas are indicating consumption of fluoridated water for prolonged period. The groundwater samples were mainly Na–Ca–HCO₃ type and rock dominance indicating the dissolution of minerals taking place. Ion exchange between OH^? ion and F^? ion present in fluoride-bearing mineral is the most dominant mechanism of fluoride leaching. High concentration of Na⁺ and HCO₃ ^? increases the alkalinity of the water, providing a favorable condition for fluoride to leach into groundwater from its host rocks and minerals.     

Provenance and weathering history of Mesoproterozoic clastic sedimentary rocks from the basal Gulcheru Formation,Cuddapah Basin

Geochemical analysis for the Mesoproterozoic clastic sedimentary rocks of the basal Gulcheru Formation of the Cuddapah Basin in the Gugudu-Dadithota-Parnapalle-Palkonda region (extending atleast 40 km) have been performed to highlight their provenance and weathering history. The low K₂O/Al₂O₃ ratios of the representative samples points to the recycled nature of sediments and illite clay in the sediments indicate an overall cold climate (low chemical weathering degree). All the provenance diagrams indicate a mixed source of the Gulcheru sediments with felsic dominancy and Upper continental crust (UCC) signature.     

Assessment of natural radioactivity in aquifer medium bearing uranium ores in Koprubasi,Turkey

Koprubasi, located within Manisa Province near the Izmir, is the biggest uranium mine where uranium ores originate from Neogene aged altered sandstone and conglomerate layers. The main objective of this study is to determine the radiation hazard associated with radioactivity levels of uranium ores, and the rocks and sediments around Koprubasi. In this regard, measured activity levels of ²²⁶Ra, ²³²Th and ⁴⁰K were compared with world averages. The average activity levels of ²²⁶ Ra, ²³²Th and ⁴⁰K were measured to be 5369.75, 124.78 and 10.0 Bq/kg in uranium ores, 24.32, 52.94 and 623.38 Bq/kg in gneiss, 46.24, 45.13 and 762.26 Bq/kg in sandstone and conglomerate, 73.11, 43.15 and 810.65 Bq/kg in sediments, respectively. All samples have high ²²⁶Ra and ⁴⁰K levels according to world average level. As these sediments are used as construction materials and in agricultural activities within the study area, the radiation hazard are calculated by using dose rate (D), annual effective dose rate (He), radium equivalent activity (Ra_eq) and radiation hazard index (I_yr). All the samples have Ra_eq levels that are lower than the world average limit of 370 Bq/kg. On the other hand, D, He and I_yr values are higher than world average values. These results indicate that the uranium ores in the Koprubasi is the most important contributor to the natural radiation level. The radioactivity levels of sediments and rocks make them unsuitable for use as agricultural soil and as construction materials. Moreover, it is determined that shallow groundwater in sediments and deep groundwater in conglomerate rocks and also surface water sources in the Koprubasi have high ²²⁶Ra content. According to environmental radioactive baseline, some environmental protection study must be taken in Koprubasi uranium site and the environment.     

Geochemical Atlas of Finland: preliminary aspects

During 1984 and 1985, the Geological Survey of Finland carried out regional geochemical mapping of till, at a scale of 1:2,000,000, as part of a programme to produce data for the first Geochemical Atlas of Finland. The Atlas is designed to give comprehensive background information on the distribution of elements in rocks, soils, and the surficial environment.