Geochemistry of Archaean volcanic rocks from Iron Ore Supergroup, Singhbhum, eastern India     

S. Sengupta  S. K. Acharyya  J. B. DeSmeth 《Journal of Earth System Science》1997,106(4):327-342

Mafic-ultramafic rocks of Archaean age constitute a significant component of the Eastern Indian Craton. These occur in two different modes. In the eastern belt these occur as a long, linear enclave within the Singhbhum granite and the primary banding in them is subvertical. In the more extensive western belt along the periphery of the Singhbhum granite, the disposition of the primary banding is subhorizontal. The major rock type in both the belts is meta-basalt with minor peridotitic komatiite and basaltic komatiite occurring in the eastern belt. Rare ultramafic rocks with cumulate textures are present in both the belts. The larger volume of the basaltic rocks preclude the possibility of their being derived by fractional crystallization of the high-MgO components. On the basis of trace element and REE characters the rocks may be classified into three groups. One of the groups shows a tholeiitic trend and include samples mostly from the eastern belt while the second consisting mostly of samples from the western belt shows a calc-alkaline trend. The third group includes samples having elemental ratios intermediate between these two groups. Zr/Nb ratios for the tholeiitic and calc-alkaline samples are different suggesting their sources to be different. The tholeiitic samples have been generated from a source having chondritic REE characters, while the calc-alkaline samples have been generated from a source with LREE enriched character. The high-MgO components in both the groups are suggested to represent high degrees of melting compared to the basalts in each group. It is further suggested that the tholeiitic basalts have been generated relatively early from a chondritic source. Down-buckling of this material has added LREE enriched melts to the source, thereby changing its character into a LREE enriched one. Melting of a source with such changed character has subsequently produced the calc-alkaline melts. Rocks with variable but intermediate characters between these two groups have been generated as a result of contamination between these two groups.  相似文献   

吉林省板石沟铁矿矿区地质特征   总被引：2，自引：0，他引：2  

屈奋雄  张宝华  崔文智 《吉林地质》1992,(3)

本文认为吉林省板石沟铁矿区为一太古宙绿岩带发育区;铁矿相当于G.A.Gross的阿尔戈马型;矿区鞍山群地层在太古宙末期经历了一次强塑性变形—D_1,它置换了矿区地层,产生了一套透入性的S+F+L构造;这期构造变形发生在低角闪岩相条件下,它控制着板石沟铁矿矿体的形态、厚度、展布及延伸。  相似文献   

青林省含铁地下水的分布与处理措施     

滕继奎 《吉林地质》1992,(4)

本文根据含铁地下水的形成条件将吉林省含铁地下水划分为四个区,并论述了各区的分布特征。综合国内目前各种地下水除铁技术,着重对各除铁系统的方法、基本原理和适用条件以及经济效益等进行了论述。从环境水文地质学的角度,提出了在含铁地下水区寻找低铁地下水的方法,并通过实例验证是可行的。  相似文献   

Immobilization of Cu and As in two contaminated soils with zero-valent iron – Long-term performance and mechanisms     

《Applied Geochemistry》2016

Immobilization of trace elements in contaminated soils by zero-valent iron (ZVI) is a promising remediation method, but questions about its long-term performance remain unanswered. To quantify immobilization and predict possible contaminant remobilization on long timescales detailed knowledge about immobilization mechanisms is needed. This study aimed at assessing the long-term effect of ZVI amendments on dissolved copper and arsenic in contaminated soils, at exploring the immobilization mechanism(s), and at setting up a geochemical model able to estimate dissolved copper and arsenic under different scenarios. Samples from untreated and ZVI-treated plots in two field experiments where ZVI had been added 6 and 15 years ago were investigated by a combination of batch experiments, geochemical modeling and extended X-ray absorption fine structure (EXAFS) spectroscopy. Dissolved copper and arsenic concentrations were described by a multisurface geochemical model with surface complexation reactions, verified by EXAFS. The ZVI remained “reactive” after 6–15 years, i.e. the dissolved concentrations of copper and arsenic were lower in the ZVI-treated than in the untreated soils. There was a shift in copper speciation from organic matter complexes in the untreated soil to surface complexes with iron (hydr)oxides in the ZVI-treated soil. The pH value was important for copper immobilization and ZVI did not have a stabilizing effect if pH was lower than about 6. Immobilization of arsenic was slightly pH-dependent and sensitive to the competition with phosphate. If phosphate was ignored in the modeling, the dissolution of arsenate was greatly underestimated.  相似文献   

The Effect of Organic Carbon-Iron Oxide Association on the Preservation of Sedimentary Organic Carbon in Marine Environments   总被引：1，自引：0，他引：1  

Zhao Bin  Yao Peng  Yu Zhigang 《地球科学进展》2016,31(11):1151-1158

Understanding the mechanisms responsible for long-term storage of organic carbon (OC) in marine environment is important for studying the marine carbon cycling and predicting how the global carbon cycle will respond to climate change. It is estimated that more than 20% of the OC in marine sediments is associated with iron oxides and thus these complexes are one of the most important factors in the long-term storage of OC. The OC-iron oxide (OC-Fe) association can be formed through either adsorption or co-precipitation, but the dominant mechanism of OC-Fe association in marine environments is co-precipitation. The combination of OC from different sources with iron oxides is selective. Iron oxides preferentially combine with marine OC in most marine environments, but in estuarine delta regions they prefer terrestrial OC. Due to large inputs of terrestrial materials, high primary production and frequent re-suspension, estuarine and marginal seas are suitable sites for OC-Fe association studies, which should be emphasized in the future.  相似文献   

Fluxes of iron and manganese across the sediment–water interface under various redox conditions     

Svetlana V. Pakhomova  Per O.J. Hall  Mikhail Yu. Kononets  Alexander G. Rozanov  Anders Tengberg  Andrei V. Vershinin 《Marine Chemistry》2007

Fluxes of dissolved forms of iron and manganese across the sediment–water interface were studied in situ in the Gulf of Finland and the Vistula Lagoon (Baltic Sea), and in the Golubaya Bay (Black Sea) from 2001 to 2005. Fluxes were measured using chamber incubations, and sediment cores were collected and sliced to assess the porewater and solid phase metal distribution at different depths. Measured and calculated benthic fluxes of manganese and iron were directed out of sediment for all sites and were found to vary between 70–4450 and 5–1000 µmole m^− 2 day^− 1 for manganese and iron, respectively. The behavior of the studied metals at various redox conditions in the near-bottom water and in the sediment was the main focus in this study. Our results show the importance of bottom water redox conditions for iron fluxes. We measured no fluxes at oxic conditions, intermediate fluxes at anoxic conditions (up to 200 μmole m^− 2 day^− 1) and high fluxes at suboxic conditions (up to 1000 μmole m^− 2 day^− 1). Total dissolved iron fluxes were generally dominated by iron(II). Contribution of iron(III) to the total iron flux did not exceed 20%. Obtained fluxes of manganese at all studied regions showed a linear correlation (r² = 0.97) to its concentration in the porewater of the top sediment layer (0–5 mm) and did not depend on dissolved oxygen concentrations of bottom water. Organically complexed iron and manganese were in most cases not involved in the benthic exchange processes.  相似文献   

Parameterization of iron and manganese cycling in the Black Sea suboxic and anoxic environment     

Sergey Konovalov  Anatoliy Samodurov  Temel Oguz  Leonid Ivanov 《Deep Sea Research Part I: Oceanographic Research Papers》2004,51(12):273

New and published data on the distribution and speciation of manganese and iron in seawater are analyzed to identify and parameterize major biogeochemical processes of their cycling within the suboxic (15.6σ_t16.2) and anoxic layers (σ_t16.2) of the Black Sea. A steady-state transport-reaction model is applied to reveal layering and parameterize kinetics of redox and dissolution/precipitation processes. Previously published data on speciation of these elements in seawater are used to specify the nature of the transformations. Two particulate species of iron (Fe(III) hydroxide and Fe(II) sulfide) are necessary to adequately parameterize the vertical profile of suspended iron, while three particulate species (hydrous Mn(IV) oxide, Mn(II) sulfide, and Mn(II) carbonate) are necessary to describe the profile of suspended manganese. In addition to such processes as mixing and advection, precipitation, sinking, and dissolution of manganese carbonate are found to be essential in maintaining the observed vertical distribution of dissolved Mn(II). These results are used to interpret the observed difference in the form of vertical distribution for dissolved Mn(II) and Fe(II). Redox transformations of iron and manganese are coupled via oxidation of dissolved iron by sinking suspended manganese at σ_t16.2±0.2 kg m⁻³. The particulate manganese, necessary for this reaction, is supplied through oxidation of dissolved Mn(II). The best agreement with observations is achieved when nitrate, rather than oxygen, is set to oxidize dissolved Mn(II) in the lower part of the suboxic layer (15.90σ_t16.2). The results support the idea that, after sulfides of these metals are formed, they sink with particulate organic matter. The sinking rates of the particles and specific rates of individual redox and dissolved-particulate transformations have been estimated by fitting the vertical profile of the net rate.  相似文献   

Mesozooplankton responses to iron-fertilization in the western subarctic Pacific (SEEDS2001)   总被引：1，自引：1，他引：1  

Atsushi Tsuda  Hiroaki Saito  Jun Nishioka  Tsuneo Ono 《Progress in Oceanography》2005,64(2-4):237

A mesoscale iron-fertilization experiment was carried out in the western subarctic Pacific during summer 2001. The iron-patch was traced for 14 days after the fertilization, and the abundance and behavior of mesozooplankton were compared with those outside of the patch. The phytoplankton biomass in the patch rapidly increased to over 15 times the initial level by the later half of the observation period, and was composed of large-sized (>10 mm), centric diatoms. Dominant zooplankton species in the upper 200-m depth were large copepods: Neocalanus plumchrus, Neocalanus cristatus, Eucalanus bungii and Metridia pacifica. Mesozoplankton biomass as well as species composition did not change significantly in the patch over the observation period. Furthermore, no changes of vertical distribution or diel vertical migration were observed for any species or stages of mesozooplankton throughout the observation period. However, the abundance of the first copepodite stages of N. plumchrus and E. bungii increased several fold in the patch after the diatom bloom formation compared to the densities outside the patch. The increases of both species are considered to be due to lowered mortality during the egg and nauplius stages. Spawning of N. plumchrus takes place at depth using lipid storage, while spawning of E. bungii takes place in the surface layer supported by grazing. These facts suggest that the relative importance of nauplii in the diets of the large copepods was decreased in the patch by the diatom bloom. Gut-pigment contents of dominant copepods in the patch increased 4–18 times, and the maximum values were observed during the bloom peak. However, the grazing impact on phytoplankton was low throughout the experiment, especially during the bloom period (<6% of the primary production).  相似文献   

西南三江金厂河矽卡岩型多金属矿床铁同位素分馏机制及其对成矿物质来源的制约SCIEI北大核心CSCD     

陈福川  程晓林  韩润生  李龚健  刘金宇  常河  贾祯  程岩 《岩石学报》2022,38(1):157-171

金厂河矿床是西南三江成矿省保山地块最具代表性的远端矽卡岩型多金属矿床之一,查明其成矿金属来源对理解该类矿床成因以及区域成矿规律具有重要意义。本文通过分析不同成矿阶段代表性含铁矿物的铁同位素组成,探讨其在成矿过程中的分馏机制,从而示踪成矿金属的源区特征。金厂河矽卡岩型矿床中成矿前阶段未蚀变的石榴子石和氧化物成矿阶段的磁铁矿均相对富集铁的重同位素,其δ;Fe值分别为0.05‰~0.16‰和0.07‰~0.18‰,而硫化物成矿阶段的黄铁矿和黄铜矿则相对富集铁的轻同位素,其δ;Fe值分别为-0.12‰~0.17‰和-0.54‰~-0.38‰,整体显示出从高氧逸度的成矿前阶段向低氧逸度的硫化物成矿阶段演化过程中矿物δ;Fe值逐渐降低的趋势,指示Fe;富集铁的重同位素,Fe;富集铁的轻同位素。同时,金厂河矿床各阶段矿物的δ;Fe值均显著低于碳酸盐围岩,而接近全球花岗岩的δ;Fe值,表明成矿的铁不是由围岩贡献,而是来自于隐伏的中酸性岩体。  相似文献   

富铁橄榄石的水溶性实验研究SCIEI北大核心CSCD     

杨家英  张琼  赵永红  李杨  KOHLSTEDTDavidL 《岩石学报》2022,38(4):1280-1284

地幔的力学性质主要受橄榄石流变性的控制,含水对橄榄石流变性质的影响很大,而橄榄石的水溶性受到温度和铁含量的影响,因此,本文进行了不同铁含量橄榄石在不同温度下的水溶性实验研究。实验使用的样品为天然橄榄石单晶Fa_(17)和Fa_(24.7)(Fe_(No.)=100×molar Fe/(Mg+Fe))以及人工合成的橄榄石单晶Fa_(22);橄榄石单晶的水溶性实验在300MPa围压和1273~1473K的温度条件下进行,每隔50K进行一组实验,氧逸度被控制在Ni NiO水平上。实验结束后,对橄榄石单晶沿b面进行双面研磨抛光,用电子探针分析确定橄榄石单晶成分,采用EBSD精确测量橄榄石的单晶方向,使用红外光谱仪(FTIR)的非偏振光路测试橄榄石单晶在b轴上的吸收光谱。对FTIR吸收光谱进行积分得到富铁橄榄石的水溶性实验结果:当温度由1273K升至1473K时,橄榄石单晶Fa_(17)的水溶性变化为600~1200H/10^(6) Si,橄榄石单晶Fa_(24.7)的水溶性变化为1000~1300H/10^(6) Si,人工合成的橄榄石单晶Fa_(22)的水溶性变化为500~900 H/10^(6) Si。因此,相同铁含量橄榄石单晶的水溶性随温度的增加而增加,相同温度条件下,天然形成的橄榄石的水溶性随着铁含量的增加而增加,百分之一的铁含量的增加,可以导致约百分之十的水溶性的增加。本文所研究的不同铁含量的橄榄石可以为更好地估算上地幔水溶性提供依据。  相似文献