It is well known that the Hetao Basin is one of the most seriously arsenic-affected groundwater areas in China. In order to understand the characteristics of high arsenic(As) groundwater in the Basin, a brief overview of arsenic in groundwater follows. High arsenic in the Basin commonly occurs in shallow groundwater and the total arsenic concentrations range from 0.58 to 572 μg/L(average 99.73 μg/L), exceeding the maximum mandated value of 10 μg/L for drinking water in China; As(Ш) is the predominant species. The regional distribution pattern of arsenic in the groundwater increases from south/southeast to north/northwest. Hangjinhouqi and Wuyuan counties are considered as the most seriously affected areas, with high incidences of endemic arsenicosic diseases in the Hetao Basin. High groundwater arsenic correlates with the increase of well depth. Previous studies proposed that groundwater arsenic in the Basin is mainly originated from desorption of some natural solid materials in the sediments, under reducing condition. Generally, reducing condition is believed to be the primary factor for arsenic releasing from the sediment to groundwater in the region. Under inorganic or bacterial processes, Fe2O3 changes to Fe S and arsenic adsorbed to Fe(OH)3 dissolves into groundwater, and As(V) is reduced to As(Ш). Besides, reducing environments, groundwater hydraulic gradients, organic matter, p H, evapotranspiration, and soil texture are presumed to be the predominant factors that control arsenic mobilization. 相似文献
A large amount of deep oil has been discovered in the Tazhong Uplift, Tarim Basin whereas the oil source is still controversial. An integrated geochemical approach was utilized to unravel the characteristics, origin and alteration of the deep oils. This study showed that the Lower Cambrian oil from well ZS1C (1x) was featured by small or trace amounts of biomarkers, unusually high concentration of dibenzothiophenes (DBTs), high δ34S of DBTs and high δ13C value of n-alkanes. These suggest a close genetic relationship with the Cambrian source rocks and TSR alteration. On the contrary, the Middle Cambrian oils from well ZS1 (2a) were characterized by low δ13C of n-alkanes and relatively high δ34S of individual sulfur compounds and a general “V” shape of steranes, indicating a good genetic affinity with the Middle–Upper Ordovician source rocks. The middle Cambrian salt rock separating the oils was suggested to be one of the factors responsible for the differentiation. It was suggested that most of the deep oils in the Tazhong Uplift were mixed source based on biomarkers and carbon isotope, which contain TSR altered oil in varied degree. The percentage of the oils contributed by the Cambrian–Lower Ordovician was in the range of 19–100% (average 57%) controlled by several geological and geochemical events. Significant variations in the δ34S values for individual compounds in the oils were observed suggesting a combination of different extent of TSR and thermal maturation alterations. The unusually high DBTs concentrations in the Tazhong-4 oilfield suggested as a result of mixing with the ZS1C oil (1x) and Lower Ordovician oils based on δ34S values of DBT. This study will enhance our understanding of both deep and shallow oil sources in the Tazhong Uplift and clarify the formation mechanisms of the unusually high DBTs oils in the region. 相似文献
A procedure for determining a wide range of chalcophile and siderophile elements in typical crustal rocks using standard addition and ICP‐SFMS (inductively coupled plasma sector field mass spectrometry) is presented. New results for Ga, Ge, Mo, Ag, Cd, In, Sn, Sb, W, Tl and Bi abundances in USGS whole‐rock reference materials AGV‐2, BHVO‐1, BIR‐1, G‐2, GSP‐1 and W‐2 are reported using this analytical procedure. Intermediate precision of means based on multiple dissolved aliquots of each USGS reference material was 10% RSD or better for Ga, Ge, In and Sn in all, and similarly good for Ag, Cd, Sb, Tl and Bi in most reference materials. Poorer intermediate precision of Mo and W measurements in several reference materials is probably due to higher analytical blanks on these elements and powder heterogeneity due to a sulfide‐related nugget effect in the specific case of Mo in GSP‐1. Results for all elements fell within the range of available published data with the exception of Ag, which yielded systematically higher concentrations than found in the literature for five of the six reference materials, likely reflecting interference from unresolved polyatomic species. 相似文献
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