Distribution and reactivity of oxyanions (Sb, As, V, Mo) in the surface freshwater reaches of the Gironde Estuary (France)

The present work reports on the temporal variations of Sb, As, V and Mo concentrations in the surface freshwater reaches of the Gironde Estuary (SW France). Dissolved (<0.2 and <0.02 μm) and particulate Sb, As, V and Mo concentrations were measured in samples collected with high temporal resolution (every 30 min) during two consecutive tides at a fixed station located upstream of the city of Bordeaux and the maximum turbidity zone (MTZ). In addition, measurements of suspended particulate matter concentration, physico-chemical parameters, Cl⁻ concentration, water depth, current velocity and particulate Th concentration were performed either at the same time resolution or continuously. The data obtained suggested that variations in particulate As, V and Mo concentrations were most probably related to tidal cycling near the sampling site of fine grained particles from the MTZ located downstream. Significant differences in the behavior of the dissolved target oxyanions, mostly present in the <0.02 μm fraction, occurred. The behavior of Sb was conservative. Variations of the dissolved As and V concentrations showed similar cycling trends, strongly related to tidal cycles. These As and V cycles were interpreted as a mixing between upstream freshwater and downstream water enriched in dissolved As and V by desorption from the MTZ particles. The observed trend in the variation of the dissolved Mo was more complex than that of As and Sb and attributed to the mixing of the water bodies mentioned above coupled to a point source input of dissolved Mo from an intra-estuarine source. The contribution of this suspected Mo source to the dissolved Mo concentrations measured at the sampling site was estimated from the ratio of dissolved Mo to dissolved As concentrations. The additional dissolved Mo signal, coupled to the monitored ebb and flood length and associated current velocities, suggested an anthropogenic input which may derive from industrial activity near the city of Bordeaux. Extrapolating these results to the annual scale suggested that this dissolved Mo may be equivalent to 45-90% of the annual dissolved Mo flux into the Garonne Branch, highlighting the importance to further investigate the origin and behavior of Mo in the fluvial estuary near Bordeaux.     

Biogeochemistry of trace metals (Mn, Sr, Rb, Ba, Cu, Zn, Pb and Cd) in a river-wetland-lake system (Balaton Region, Hungary)

Mn, Sr, Ba, Rb, Cu, Zn, Pb and Cd concentrations have been measured seasonally in the water and deposited sediments of the system comprising: Zala river (main input) — Lakes Kis-Balaton 1 and 2 (small artificial lakes created in a former bay of Lake Balaton) — Keszthely bay (hypertrophic part of Lake Balaton). The concentrations of the trace elements together with pH, alkalinity, dissolved cations (Ca²⁺, Mg²⁺, Na⁺, and K⁺), dissolved inorganic ligands (Cl^–, SO₄ ^2–), particulate Al, Ca, inorganic and organic carbon are used to assess the contamination of the study area and biogeochemical processes controlling trace element concentrations. Thermodynamic speciation calculations have also been utilized to enhance our understanding of the system. In the sediments Rb, Ba, Cu and Zn concentrations were mainly controlled by the abundance of the aluminosilicate fraction. Strontium was mainly associated with the calcium carbonate fraction. The aluminosilicate fraction constitutes a major sink for Mn and Cd but the concentration of these elements are also strongly related to calcite precipitation. The main processes that control the dissolved distribution of trace elements in the Balaton system were: solid phase formation (carbonate) for Mn; coprecipitation with calcite for Sr, Ba, Rb and possibly Mn and Cd; adsorption/desorption processes (pH dependent) for Zn and Pb; solubilization of Mn and precipitation of Cd and Cu in reed covered wetland areas where anoxic conditions were probably existing during the warm season. A preliminary budget of atmospheric and river input to Lake Balaton has also been outlined. Although Lake Balaton, is subjected to anthropogenic inputs mainly from agricultural and domestic activities, their impact on trace element concentrations in the Balaton system is very limited due to the efficiency of removal processes (i.e. adsorption and co-precipitation) and to high sedimentation rates and strong sediment re-suspension. Anthropogenic inputs are only detected for Pb.     

Geochemistry and Modes of Occurrence of Hazardous Trace Elements in the No. 11 Coal Seam, Antaibao Surface Mine, Shanxi Province

Concentrations of seventeen hazardous trace elements including As, Pb, Hg, Se, Cd, Cr, Co, Mo, Mn, Ni, U, V, Th, Be, Sb, Br and Zn in the No.ll coal seam, Antaibao surface mine, Shanxi Province were determined using Instrumental Neutron Activation Analysis （INAA）, Inductively Coupled Plasma Atomic Emission Spectrometry （ICP-AES）, Cold-Vapor Atomic Absorption Spectrometry （CV-AAS） and Graphite Furnace Atomic Absorption Spectrometry （GF-AAS）. Comparisons with average concentrations of trace elements in Chinese coal show that the concentrations of Hg and Cd in the No. 11 coal seam, Antaibao surface mine are much higher. They may be harmful to the environment in the process of utilization. The variations of the trace elements contents and pyritic suffur in vertical section indicated that： （a） the concentrations of As, Pb, Mn, and pyritic sulfur decrease from roof to floor; （b） the concentrations of Cr, Zn and Mo are higher in roof, floor and lower in coal seam; （c） the concentration of Br, Sb, and Hg are higher in coal seam and lower in roof and floor; （d） the concentrations of Mo, V, Th and AI vary consistently with the ash yield. Cluster analysis of trace elements, pyritic sulfur, ash yield and major elements, such as AI, Fe, P, Ca shows that： （a） pyritic sulfur, Fe, As, Mn, Ni, Be are closely associated and reflect the influence of pyrite; （b） Mo, Se, Pb, Cr, Th, Co, Ca and A! are related to clay mineral, which is the main source of ash; （c） U, Zn, V, Na, P maybe controlled by phosphate or halite; （d） Hg, Br, Sb and Cd may be mainly organic-associated elements which fall outside the three main groups. The concentration distribution characteristics of trace elements in coal seam and the cluster analysis of major and trace elements showed that the contents of trace elements in the No. 11 coal seam, Antaibao surface mine, are mainly controlled by detrital input and migration from roof and floor.     

Abundances and modes of occurrence of trace elements in the Çan coals (Miocene), Çanakkale-Turkey

This study presents the concentrations and modes of occurrence of trace elements in 81 coal samples from the Çan basin of northwestern Turkey. The concentration of trace elements in coal were determined by inductively coupled plasma-mass spectrometry and inductively coupled plasma-atomic emission spectrometry. Additionally, traditional coal parameters were studied by proximate, ultimate, X-ray diffraction, and petrographic analyses. Twenty trace elements, including As, B, Ba, Be, Cd, Cu, Co, F, Hg, Mo, Ni, Pb, Sb, Se Sn, Th, Tl, U, V, and Zn, receive much attention due to their related environmental and human health concerns. The Çan coals investigated in this study are lignite to sub-bituminous coal, with a broad range of ash yields and sulphur contents. The trace element concentrations show variety within the coal seams in the basin, and the affinities vary among locations. The concentrations of B, Ba, Be, Cd, Cu, Co, F, Hg, Mo, Ni, Pb, Sb, Se, Sn, Tl, and Zn in Çan coals are within the Swaine's worldwide concentration range, with the exception of As, Th, U, and V. On the other hand, compared with world coals, the Çan basin coals have higher contents of As, B, Cu, Co, Mo, Pb, Th, U, V, and Zn. Based on statistical analyses, most of the trace elements, except for U, show an affinity to ash yield. Elements including As, Cd, Hg, Se, Cu, Mo, Ni, and Zn, show a possible association with pyrite; however, the elements Se, B, and Mo can be have both organic and inorganic associations.     

Concentration and distribution of trace elements in some coals from Northern China

The concentration, distribution and modes of occurrence of trace elements in thirty coals, four floors and two roofs from Northern China were studied. The samples were collected from the major coalfields of Shanxi Province, Shaanxi Province, Inner Mongolian Autonomous Region, and Ningxia Hui Autonomous Region. The concentrations of seventeen potential hazardous trace elements, including Hg, As, Se, Pb, Cd, Br, Ni, Cr, Co, Mo, Mn, Be, Sb, Th, V, U, Zn, and five major elements P, Na, Fe, Al, and Ca in coals were determined.Compared with average concentration of trace elements in Chinese coal, the coals from Northern China contain a higher concentration of Hg, Se, Cd, Mn, and Zn. They may be harmful to the environment in the process of combustion and utilization. Vertical variations of trace elements in three coal seams indicated the distributions of most elements in coal seam are heterogeneous. Based on statistical analyses, trace elements including Mo, Cr, Se, Th, Pb, Sb, V, Be and major elements including Al, P shows an affinity to ash content. In contrast, Br is generally associated with organic matter. Elements As, Ni, Be, Mo, and Fe appear to be associated with pyrite. The concentrations of trace elements weakly correlate either to coal rank or to maceral compositions.     

Mode of occurrence of trace elements in the Pellana lignite (SE Peloponnese,Greece)

Mineralogical and geochemical analyses of the Pellana lignite (SE Peloponnese, Greece) were carried out in order to predict the mode of occurrence of trace elements and their mobility during lignite combustion for power generation. Lignite and ash samples (after combustion at 750 °C) of two cores from this deposit were examined. The mean ash content is 30% to 43% and C contents on dry, ash-free basis range from 45% to 60%, respectively. The mineral phases contained in the lignite are quartz, K-feldspars, mixed-layer clays (illite-rich), micas, gypsum and pyrite. Factor analysis on geochemical data shows that the elements As, Ba, Mn, Mo, Sb, Se, Sr, U and V have both organic and inorganic affiliation. To study the mobility of each element during combustion, the relative enrichment factor was calculated. The most depleted and hence the most mobile elements, proved to be Hf, Nb and Sb, while Se, Ba and Bi are moderately depleted. In case of the Pellana lignite utilization we should expect environmental problems associated with the elements As, Ba, Bi, Hf, Mn, Mo, Nb, Sb and Se. These elements may be either volatilized during combustion or leached from fly ash-disposal areas into underground waters, causing severe environmental and health impacts.     

晋北-宁北煤中痕量元素的地球化学特征

应用仪器中子活化 (INAA)、电感耦合等离子体原子发射光谱 (ICP- AES)和原子吸收光谱 (AAS)等方法测定了晋北-宁北一线 5对矿井、 2个露天矿、 5个电厂和 3个洗煤厂煤中环境敏感性痕量元素的含量;通过与中国土壤、其他地区煤以及世界范围煤中痕量元素含量进行对比,总结了研究区痕量元素的分布、富集特征,得知部分地区煤中 Hg、 Cd和 Se的含量较高,在燃烧利用过程中可能对环境造成影响.通过分析痕量元素与灰分、挥发分的相关性以及痕量元素间、痕量元素与 Al、 Fe和 Sp的相关、聚类特性,探讨了痕量元素间及其与矿物质间的亲合性及赋存特征.     

Spatial distribution of metals in urban topsoils of Xuzhou (China): controlling factors and environmental implications

The contamination of soils by metals from various sources is a subject of increasing concern in recent times. Twenty-eight elements (Fe, Ti, Cr, Al, Ga, Pb, Sc, Ba, Li, Cd, Be, Co, Cu, Mn, Ni, V, Zn, Mo, Pt, Pd, Au, As, Sb, Se, Hg, Bi, Ag and Sn) have been analyzed from urban topsoil from the city of Xuzhou. The concentrations of these analyzed elements have been correlated to some soil parameters such as organic matter, pH, cation exchange capacity, carbonate content, and granulometric fractions (clay, silt and sand). Results of the statistical analysis show a large variety and complexity in these relationships. The spatial distributions of these metal concentrations were also constructed using geographical information system. The spatial distribution patterns of the elements analyzed show that traffic and industrial activities are the principal anthropogenic pollutant sources.     

Platinum and Palladium in Coal Rock and Geochemical Anomaly in Eastern Yunnan Province,Southwest China

A series of geochemical anomalies of Pt and Pd were found in 1 358 recombined samples from a geochemical stream sediment survey in eastern Yunnan (云南) Province, China. Chemical optical emission spectroscopy, X-ray fluorescence analysis, and inductively coupled plasmas atomic emission spectrometry analyses of 22 elements and chemical compositions of 21 samples from coal-bearing strata from the Late Paleozoic, Mesozoic, and Cenozoic show Pt and Pd concentrated to some extent in coal rocks, with Pd/Pt相似文献   

Taxonomical and Biogeochemical Investigation of Elements in Holocene Mollusk Shells in the South and Southwestern Marmara Basin, Turkey

Concentrations of some heavy metals and trace elements such as Cr,Ga,Ni,Zn,Mo,Cu, Pb,Yb,Y,Nb,Ti,Sr,Ba,Mn,Sc,Co,V,Zr,Fe,Al,W,Se,Bi,Sb,As,Cd in recent mollusk shells and factors affecting their distribution and deposits collected from various depths in the southern and southwestern parts of the Marmara Sea are investigated.The distribution of the elements in the shells is categorized into four groups.Of these,concentrations of 12 elements(As,Bi,Cd,Co,Ga,Mo,Nb, Sb,Se,Sc,W and Yb)are below zero [(0.053-0.79)×10~(-6)];concentrations of seven elements(Cr,Ni, Pb,V,Y,Zr and Cu)are(1.0-6.0)×10~(-6);concentrations of four elements(Ti,Mn,Ba and Zn)are 10- 20×10~(-6);and concentrations of five elements(Si,Al,Fe,Mg and Sr)are(47.44-268.11)×10~(-6).The taxonomic characteristics of the 29 elements were studied separately in mollusk shells such as Chamalea gallina(Linné),Pitar-rudis(Poll),Nassarius reticulatus(Linné),Venerupis senescens (Coocconi),Mytilus galloprovincialis(Lamarck),Mytilaster lineatus(Gemelin in Linné)and Chlamys glabra.It was found that,in mollusk taxonomy,the elements have unique values.In other words, element concentrations in various mollusk shells depend mainly on the taxonomic characteristics of mollusks.In various bionomic environments different element distributions of the same species are attributed to the different geochemical characters of the each environment.Data obtained in this study indicate that the organisms are the most active and deterministic factors of the environment.     

Heavy metal concentrations in sultana-cultivation soils and sultana raisins from Manisa (Turkey)

This paper describes the concentrations of heavy metals in soils and in raisins (sultanas) cultivated upon the Gediz Plain (Manisa), western Turkey, which is cut by major roads from ?zmir to ?stanbul and ?zmir to Ankara. A total of 212 samples of surface soil and 82 raisin samples were analysed. Soil samples have nearly same mineralogy, quartz, calcite, magnetite, pseudo-rutile and clay minerals. Dolomite is seen especially in areas close to Neogene sediments. Clay minerals are mainly mica (illite?Cmuscovite), chlorite/kaolinite, smectite and mixed layers (Sm-Il). The concentrations of 21 elements (Ba, Ni, Mo, Cu, Pb, Zn, Co, Mn, As, U, Sr, Cd, Sb, Bi, Cr, B, W, Hg, Sn, Li and organic C) were determined in the surface soils. The degree of element enrichment in soil can be measured in many ways, the most common of which are the geoaccumulation index (Igeo), enrichment factor and the pollution index. Arsenic and Sb showed the highest Igeo values, corresponding to Igeo classes 3?C4. Hence, the area is characterised as ??being heavily contaminated to polluted?? by As and Sb. Arsenic contamination has been reported from all over world. Arsenic-related pollutants enter the groundwater system by gradually moving with the flow of groundwater from rains and irrigation. Gediz Plain forms the main groundwater supply of ?zmir city. The enrichment factor (EF_arsenic) of the analysed soil samples is around 76, which corresponds to ??extremely high enrichment??. The concentrations of 33 elements (Al, Sb, As, Ba, Be, Bi, B, Cd, Ca, Cr, Co, Cu, Fe, Pb, Li, Mg, Mn, Hg, Mo, Ni, K, Se, Ag, Na, Sr, Ta, Th, Sn, Ti, U, V, Zn and Zr) were determined in the raisin samples. The Pb and Cd contents of raisins are of great concern due to their toxicity. Pb contents ranged between 0.05 and 0.46?mg?kg^?1, and average Cd content was 0.04?mg?kg^?1. Only one sample contained high level of Cd, 0.23?mg?kg^?1. After cleaning the raisins, the heavy metal concentrations were low as in the European Community (EC) regulation No: 466/2001 for allowable levels of Pb (0.2?mg?kg^?1) and Cd (0.05?mg?kg^?1).     

Pedo-geochemical baseline content levels and soil quality reference values of trace elements in soils from the Mediterranean (Castilla La Mancha, Spain)

To evaluate trace element soil contamination, geochemical baseline contents and reference values need to be established. Pedo-geochemical baseline levels of trace elements in 72 soil samples of 24 soil profiles from the Mediterranean, Castilla La Mancha, are assessed and soil quality reference values are calculated. Reference value contents (in mg kg^?1) were: Sc 50.8; V 123.2; Cr 113.4; Co 20.8; Ni 42.6; Cu 27.0; Zn 86.5; Ga 26.7; Ge 1.3; As 16.7; Se 1.4; Br 20.1; Rb 234.7; Sr 1868.4; Y 38.3; Zr 413.1; Nb 18.7; Mo 2.0; Ag 7.8; Cd 4.4; Sn 8.7; Sb 5.7; I 25.4; Cs 14.2; Ba 1049.3; La 348.4; Ce 97.9; Nd 40.1; Sm 10.7; Yb 4.2; Hf 10.0; Ta 4.0; W 5.5; Tl 2.3; Pb 44.2; Bi 2.2; Th 21.6; U 10.3. The contents obtained for some elements are below or close to the detection limit: Co, Ge, Se, Mo, Ag, Cd, Sb, Yb, Hf, Ta, W, Tl and Bi. The element content ranges (the maximum value minus the minimum value) are: Sc 55.0, V 196.0, Cr 346.0, Co 64.4, Ni 188.7, Cu 49.5, Zn 102.3, Ga 28.7, Ge 1.5, As 26.4, Se 0.9, Br 33.0 Rb 432.7, Sr 3372.6, Y 39.8, Zr 523.2, Nb 59.7, Mo 3.9, Ag 10.1, Cd 1.8, Sn 75.2, Sb 9.9, I 68.0, Cs 17.6, Ba 1394.9, La 51.3, Ce 93.5, Nd 52.5, Sm 11.2, Yb 4.2, Hf 11.3, Ta 6.3, W 5.2, Tl 2.1, Pb 96.4, Bi 3.0, Th 24.4, U 16.4 (in mg kg^?1). The spatial distribution of the elements was affected mainly by the nature of the bedrock and by pedological processes. The upper limit of expected background variation for each trace element in the soil is documented, as is its range as a criterion for evaluating which sites may require decontamination.     

Diel variation of arsenic,molybdenum and antimony in a stream draining natural As geochemical anomaly

The Mokrsko Stream in the central Czech Republic is an oxic and slightly alkaline stream that drains a natural As geochemical anomaly. Although long-term monitoring has characterized the general seasonal trends in trace element concentrations (i.e., As, Mo, Cu, Zn) in this stream, little is known about solubility controls and sorption processes that influence diel cycles in trace element concentrations. Trace elements (including As species, Cu, Mn, Mo, Pb and Sb) and other parameters were monitored over two 24-h periods in unfiltered and filtered (0.1 μm) samples collected in August 2010 and June 2011. Copper and Pb were predominantly (>92% of the mass) associated with the particulate fraction (>0.1 μm). Arsenic, Mo and Sb were predominantly (>88% of the mass) in the “dissolved” (<0.1 μm) form. Particulate-associated elements displayed up to a factor of 13 differences between minimum and maximum concentrations, most likely due to increased streamflow related to rainfall events. Dissolved concentrations of the trace metal cations (Cu, Fe, Mn and Pb) were consistently low and displayed no diel trends. Dissolved As(V), Mo and Sb varied on a diel cycle, with increased concentrations (up to 36%) during the late afternoon and decreased concentrations during the nighttime. Diel trends in trace anionic elements are explained by temperature-dependent sorption, as the diel changes in pH during base flow were very small (0.07 std. units). Very low concentrations of As(III), which have been shown to vary in a diel cycle, were attributed to enhanced hydraulic exchange with As(III)-rich hyporheic water during rainfall events.     

Geochemical features of aerosols in Santiago de Chile from time series analysis

Santiago, the capital of Chile, suffers from high air pollution levels, especially during winter. An extensive particulate matter (PM) monitoring and analysis program was conducted to quantify elemental concentrations of PM. Size-resolved PM samples (PM_2.5 and PM_10–2.5) from the La Paz and Las Condes stations in Santiago (2004–2005) were analyzed using ICP-MS. Most trace element concentrations (Cu, Pb, Zn, Mn, V, Sb, Pb and As) were higher during winter than during summer and were also higher at the La Paz station than at the Las Condes station. During the highest pollution events, As concentrations in PM_2.5 (16 ng m^?3) exceeded the annual average standard value (6 ng m^?3). A 10-year time series showed decreasing Pb and As concentrations and slightly increasing Zn, Cu and Mn concentrations. Concentrations of Cr and Ni remained relatively constant. The implementation of new public policies in 1998 may explain the decreasing concentrations of Pb and As. Enrichment factor (EF) calculations identified two principal groups: elements with EF < 10 (Mg, Y, Zr, U Sr, Ca, Ti, and V) and EF > 10 (Rb, K, Cs, Fe, P, Ba, Mn, Ni, Cr, Co, Zn, Sn, Pb, Cu, Mo, Cd, As, Ag, and Sb), which were related to natural and anthropogenic PM sources, respectively. Three main PM sources were identified using factor analysis: a natural source (crustal matter and marine aerosol), combustion and copper smelting. Three other sources were identified using rare earth elements: fluid catalytic crackers, oil-fired power production and catalytic converters.     

Deciphering factors controlling trace element distribution in the soils of Karaduvar industrial-agricultural area (Mersin,SE Turkey)

In this study, 30 topsoil samples were collected from Karaduvar area (Mersin, SE Turkey) where at present various industrial and agricultural activities are occurring. Using a five-step ultrasound-assisted sequential extraction (UASE) procedure, trace elements in soil samples were partitioned into the following: (1) soluble-exchangeable; (2) bound to carbonates; (3) bound to Fe- and Mn-oxides; (4) bound to organic matter and sulfide compounds, and (5) residual fraction. Concentrations of 11 trace elements in the extracts were determined using ICP-MS. Total concentrations ranged between (in mg kg⁻¹) 3.35 and 7.26 for As; 1.18 and 3.96 for Cd; 10.76 and 20.26 for Co; 37.99 and 63.48 for Cr; 18.55 and 243.1 for Cu; 338.7 and 565.6 for Mn; 4.42 and 6.44 for Mo; 148 and 279.3 for Ni; 10.12 and 73.71 for Pb; 17.93 and 36.55 for V, and 25.46 and 331.7 for Zn. Factor analysis was applied to dataset in order to discriminate between natural and anthropogenic pollution sources and factors controlling the spatial distribution of trace elements in the area. Results suggest that distributions of Co, Cr, Mn, and Ni are mainly controlled by lithological factors, whereas, distributions of Cu, Pb, and Zn can be attributed to agricultural activities such as pesticide/herbicide use and fertilizer application, as well as irrigation with petroleum hydrocarbon-contaminated groundwater. Highest concentrations of Cd and Mo are generally observed around the diesel-fired thermal power plant and ATAŞ refinery. Highest concentrations of As and V are generally observed at the NW sector of the area; however, no definitive source can be designated for both of these elements.     

Enrichment of redox-sensitive trace metals (U,V, Mo,As) associated with the late Hauterivian Faraoni oceanic anoxic event

The Faraoni Level is a short-lived oxygen-deficient event that took place during the latest Hauterivian. In order to improve our understanding of the palaeoenvironmental conditions that occurred during this event, we have analysed the contents of several redox-sensitive trace elements (U, V, Mo, As, Co, Cd, Cu, Zn, Ni, Pb, Cr) from bulk limestone samples of late Hauterivian–early Barremian age from three reference sections. U, V, Mo and As show consistent and significant enrichments during the Faraoni event whereas the other redox-sensitive trace elements analysed here are not systematically enriched. In order to explain this discrepant behaviour, we propose that the Faraoni Level was deposited during a period of anoxic conditions near the sediment–water interface. The distinctive peaks in U, V, Mo and As contents are traceable throughout the three studied sections and represent a good correlation tool which helps to identify the Faraoni Level and its equivalents in the western Tethyan realm and outside of the Tethys. For example, a peak in U contents in upper Hauterivian sediments of the northwestern Pacific realm (ODP leg 185, site 1149) may well be an expression of the Faraoni event in this particular basin.     

Antimony and arsenic mobility in a creek draining an antimony mine abandoned 85 years ago (upper Orb basin,France)

Mining residues from the Sb mine of Bournac in the upper Orb River valley (Southern France), constitute an important source of As and Sb pollution. Arsenic concentrations are as high as 78 μg/L and Sb reaches 32 μg/L in the small creek draining the tailings impoundment. Although both metalloids occur mainly in oxidized form in the creek water, their behaviour differs significantly. Iron oxides are the main carrier phases for both elements in the suspended particulate matter. In oxic conditions the two elements are mainly present in water in oxidised form As(V) and Sb(V) and both field studies and laboratory experiments indicate a higher affinity of As(V) than Sb(V) for the solid phase. In the pool, which receives the water from Bournac Creek, the reductive dissolution of Fe-oxides is linked to the oxidation of small pyrite grains transported from the tailings dump. In oxic conditions Sb is released to solution more efficiently than As. Conversely, in anoxic conditions, mobilisation of As is greater than that of Sb. This is attributed to the reduction of As, which favours its mobility. Whatever the conditions, the activity of bacteria naturally present in the sediments enhances the remobilization of Sb in oxidizing conditions and that of As in reducing conditions.     

Specifics of the elemental composition of waters in environments with operating mining and ore-processing plants in the Kola North

The paper presents data on the specifics of the distributions of chemical elements in natural waters of the Kola North depending on the landscape–geochemical characteristics of the water catchment areas and aerotechnogenic pollution. The territory is subdivided into seven zones with different dominant rock types and typical landscapes. Lakes in the Kola region generally contain elevated concentrations of Cu, Ni, Co, Cr, V, Mo, U, Sb, Bi, Al, Fe, Mn, Sr, Li, Rb, Pb, Zn, Cd, La, and Ce. The waters of lakes in the influence zones of Cu–Ni mines are enriched in La, Ce, Sm, Gd, Pr, and Nd. In waterlogged landscapes, waters are enriched in certain trace elements because of their migration with humic acids. Technogenic acidic precipitation is proved to result in leaching of several elements, first of all Cd, Zn, and As (as well as other elements contained in rocks composing the water catchment areas) and their transfer into the waters.     

甘肃北山金、铜矿床红沙的植物地球化学特征及其找矿意义

北山地区植被属戈壁荒漠植被类型，主要植物群落为红沙，红沙中多数元素特别是成矿元素及其伴生元素的含量和变化系数矿区大于背景区，元素含量背景区呈对数正态分布，矿区呈偏对数正态或多峰分布，红沙中的元素组合分类背景区为Au,Cu,Pb,Zn,As,Sb,Mo,V,Mn和Ag,Sn,Sr,Ba及Ti,Cr,Co,Ni,金矿区为Au,Ag,As,Sb,Mo,Mn,Sr和Cu,Pb,Zn,Sn,Ba及Co,Ni,Ti,V,Cr,铜矿区为Cu,Pb,Zn,Mo,Au,Ag,Ba和As,Sb,Sn,Mn及Ti,V,Cr,Co,Ni,Sr，矿区红沙中浓集系数较大的元素多数在矿区岩石中的浓集系统亦较大，金，铜矿床红沙和岩石中的特征元素分别都有Au,Ag,Ag,Sb,Mo,(Mn)和Cu,Pb,(Ba,Ti,Cr)。在金，铜矿床（体上方分别发育有良好的Au和Cu的生物地球化学异常和元素组合及分带，根据红沙的地球化学特征能，判断金或铜矿种类型，并能对掩埋，隐伏金，铜矿床（体）进行定位预测。     

Assessment of elemental content of milled coal,combustion residues,and stack emitted materials: Possible environmental effects for a Canadian pulverized coal-fired power plant

Two monitoring studies were carried out at four-year intervals on a power plant that uses western Canadian subbituminous coal and generates approximately 800 Mw/h of electricity. The distributions of elements of environment concern (As, Hg, Ni, Pb, and Cd) and elements of environmental interest (B, Ba, Be, Cl, Co, Cr, Cu, Mn, Mo, Th, Se, V, U, and Zn) in milled coals, power plant ashes, and emitted materials from the stack were determined using neutron activation analysis (NAA), Inductively Coupled Plasma Emission Spectroscopy (ICPES), and Inductively Coupled Plasma-Mass spectroscopy (ICP-MS) for most elements, Graphite Furnace Atomic Absorption (GFAA) for Pb, and Cold Vapor Atomic Absorption (CVAA) for Hg.The concentrations of most of elements in milled coal are low as compared to world coals and other Canadian milled coals. For example, in both studies mercury is within the lower range of world coal. Bottom ashes from both studies have low concentrations of As, Cd, Hg, Pb, and Zn, as well as low relative enrichment factors (RE) for the same elements, indicating that they were not enriched in the bottom ash. The ESP's remove most of the elements of environmental interest as indicated by their high RE ratios of greater than > 0.7.The rates of input of elements of environmental concern (As, Cd, Hg, Pb and Ni) for this station were 23.65, 1.24, 0.54, 98.2 and 95.2 kg/day, respectively, of which only 0.20, 0.02, 0.31, 0.48 and 0.36 kg/day were emitted from the stack. Thus only a small amount of these elements found in the milled coal was emitted while most were captured in the bottom and the ESP ashes. Nickel has the highest rate of emission (0.48 kg/day) within the elements of environmental concern group. However, the Ni emitted from this station does not belong to the toxic species. The element with the lowest rate of emission is Cd (0.02 kg/day). The total emission of elements of environmental concern is 1.37 kg/day, which is low as compared their ambient concentrations in either rural or urban air. The total rate of emission of B, Ba, Be, Co, Cr, Cu, Mn, Mo, Se, Th, U, V, and Zn is 56.51 kg/day and is mostly comprised of the total emission of Ba (21.73 kg/day) and Zn (19.14 kg/day).