He-Ar-S-Pb Isotopic Compositions of Pyrite: Constraints on the Source of Ore-forming Materials of the Chengchao Skarn Iron Deposit, SE Hubei Province, Eastern China     

LI Wei  XIE Guiqing  ZHU Qiaoqiao 《《地质学报》英文版》2016,90(5):1780-1794

The Chengchao iron deposit,the largest high-grade skarn iron deposit in southeastern Hubei Province,contains considerable amounts of magnetite and by-product anhydrite.To obtain better understanding of the ore-formation process,this study carried out He-Ar-S-Pb multi-isotopic analyses on the pyrites formed during two stages of mineralization.The results indicate that the δ~(34)S values(ranging from 14.0‰ to 17.6‰) of pyrites formed from the two stages have no obvious differences,suggesting that they were not derived from a single magmatic sulfur source.The δ~(34)S values of anhydrite mostly range from 21.9‰ to 28.4‰,similar to that of the Middle Triassic sedimentary anhydrite in the Middle-Lower Yangtze River metallogenic belt(MLYRB).The Pb isotopic compositions of the pyrites of both stages are homogeneous,with values of ~(208)Pb/~(204)Pb,~(207)Pb/~(204)Pb,and~(206)Pb/~(204)Pb being 38.006-38.257,15.523-15.556,and 17.806-18.052,respectively,indicating a mixed crust-mantle source.The He-Ar results exhibit different compositions of the two stages:the ~3He/~4He(R/Ra) and ~(40)Ar/~(36)Ar values for the early-stage pyrite are 0.46-0.63 and 311-322,respectively,whereas the values for late-stage pyrite are 0.23-0.34 and 305-361,respectively.Both stages of pyrites indicate the multiple sources of the ore-forming fluids,with decreasing amount of magmatic water and increasing amount of modified meteoric water(MASW) during fluid evolution.The Triassic evaporites played an important role in the mineralization process.  相似文献   

溶剂萃取法分离锂同位素研究进展   总被引：2，自引：2，他引：0       下载免费PDF全文

肖江  贾永忠  姚颖  石成龙  孙进贺  谢绍雷  景燕 《盐湖研究》2016,24(3):62-72

锂同位素(6Li和7Li)在原子能工业中占据着重要的地位。在众多锂同位素的分离方法和体系中,溶剂萃取法是一种具有较高分离系数,并最有望实现无毒、高效分离的工业生产方法。阐述了溶剂萃取法分离锂同位素的原理,综述了醇类与酮类、烷基膦与膦酸脂类、冠醚类及其它溶剂萃取体系在锂同位素分离中的研究现状及趋势,并展望了溶剂萃取法在锂同位素分离和未来青海、西藏盐湖锂资源高值化利用中的潜在应用前景。  相似文献   

冲绳海槽中段表层沉积物物质来源的定量分离:Sr-Nd同位素方法   总被引：16，自引：2，他引：16  

孟宪伟  杜德文  吴金龙 《海洋与湖沼》2001,32(3):319-326

利用1994年85－904航次获取的冲绳海槽中段表层沉积物样品，测定其硅酸盐相的^87Sr/^86Cr和^143Nd/^144Nd比值，以定量研究冲绳海槽中段表层沉积物硅酸盐物质的来源，结果表明，冲绳海槽中段陆坡区表层沉积物硅酸盐相的^87Sr/^86Sr/^143Nd/^144Nd与东海陆架沉物硅酸盐相的^87Sr/^86Sr和^143Nd/^143Nd相当，槽底和东坡沉积物硅酸盐相的^87Sr/^86Cr和^143Nd/^144Nd值介于中国大陆硅酸盐物质和海槽水山碎屑的^87Sr/^86Sr,^143Nd/^144Nd比值之间，并大致具有两端员混合特征，利用以Sr同位素为参数的二端员混合方程进行物源定量分析的结果表明，冲绳海槽中段的西坡和槽底表层沉积物硅酸盐相以陆源物质为主，最大值为91．07％，由西向东，陆源物逐渐减少，在海槽东坡含量最小，最小值为9．93％，火山源物质在东坡含量最高，量大值为64．92％，由东向西，由北向东，火山源物质逐渐减少为零。  相似文献   

Abundance, size distribution, and stable carbon and nitrogen isotopic compositions of marine organic matter isolated by tangential-flow ultrafiltration     

Ronald Benner  Bopaiah Biddanda  Brenda Black  Matthew McCarthy 《Marine Chemistry》1997,57(3-4)

Tangential-flow ultrafiltration was used to isolate particulate and high-molecular-weight dissolved material from seawater collected at various depths and geographic regions of the Pacific and Atlantic Oceans. Ultrafiltration proved to be a relatively fast and efficient method for the isolation of hundreds of milligrams of material. Optical and electron microscopy of the isolated materials revealed that relatively fragile materials were recovered intact. Depth-weighted results of the size distribution of organic matter in seawater indicated that ˜ 75% of marine organic carbon was low-molecular-weight (LMW) dissolved organic carbon (< 1 nm), ˜ 24% was high-molecular-weight (HMW) dissolved organic carbon (1–100 nm), and ˜ 1% was particulate organic carbon (> 100 nm). The distribution of carbon in surface water was shifted to greater relative abundances of larger size fractions, suggesting a diagenetic sequence from macromolecular material to small refractory molecules. The average C:N ratios of particulate organic matter (POM) and HMW dissolved organic matter (DOM) were 7.7 and 16.7, respectively. Differences in C:N ratios between POM and HMW DOM were large and invariant with depth and geographic region, indicating that the aggregation of HMW DOM to form POM must be of minor significance to overall carbon dynamics. The stable carbon isotope composition (δ¹³C) of POM averaged −22.7%. in surface water and −25.2%. in subsurface water. Several possible explanations for the observed isotopic shift with depth were explored, but we were unable to discern the cause. The δ¹³C of HMW DOM samples was relatively constant and averaged −21.7%., indicating a predominantly marine origin for this material. The δ¹⁵N values of POM were highly variable (5.8–15.4%.), and the availability of nitrate in surface waters appeared to be the major factor influencing δ¹⁵N values in the equatorial Pacific. In the upwelling region nitrate concentrations were relatively high and δ¹⁵N values of POM were low, whereas to the north and south of the upwelling nitrate concentrations were low and δ¹⁵N values were high. The δ¹⁵N values of HMW DOM reflected the same trends observed in the POM fraction and provided the first such evidence for biological cycling of dissolved organic nitrogen (DON). Using the observed δ¹⁵N values and an estimate of meridional advection velocity, we estimated a turnover time of 0.3 to 0.5% day⁻¹ for HMW DON. These results suggest a major role for DON in the upper ocean nitrogen cycle.  相似文献   

Sources and transport of dissolved and particulate organic carbon in the Mississippi River estuary and adjacent coastal waters of the northern Gulf of Mexico   总被引：5，自引：0，他引：5  

Xu-Chen Wang  Robert F. Chen  George B. Gardner 《Marine Chemistry》2004,89(1-4):241

Dissolved organic carbon (DOC), stable carbon isotopic (δ¹³C) compositions of DOC and particulate organic carbon (POC), and elemental C/N ratios of POC were measured for samples collected from the lower Mississippi and Atchafalaya rivers and adjacent coastal waters in the northern Gulf of Mexico during the low flow season in June 2000 and high flow season in April 2001. These isotopic and C/N results combined with DOC measurements were used to assess the sources and transport of terrestrial organic matter from the Mississippi and Atchafalaya rivers to the coastal region in the northern Gulf of Mexico. δ¹³C values of both POC (−23.8‰ to −26.8‰) and DOC (−25.0‰ to −29.0‰) carried by the two rivers were more depleted than the values measured for the samples collected in the offshore waters. Strong seasonal variations in δ¹³C distributions were observed for both POC and DOC in the surface waters of the region. Fresh water discharge and horizontal mixing played important roles in the distribution and transport of terrestrial POC and DOC offshore. Our results indicate that both POC and DOC exhibited non-conservative behavior during the mixing especially in the mid-salinity range. Based on a simple two end-member mixing model, the comparison of the measured DOC-δ¹³C with the calculated conservative isotopic mixing curve indicated that there was a significant in situ production of marine-derived DOC in the mid- to high-salinity waters consistent with our in situ chlorophyll-a measurements. Our DOC-δ¹³C data suggest that a removal of terrestrial DOC mainly occurred in the high-salinity (>25) waters during the mixing. Our study indicates that the mid- to high- (10–30) salinity range was the most dynamic zone for organic carbon transport and cycling in the Mississippi River estuary. Variability in isotopic and elemental compositions along with variability in DOC and POC concentrations suggest that autochthonous production, bacterial utilization, and photo-oxidation could all play important roles in regulating and removing terrestrial DOC in the northern Gulf of Mexico and further study of these individual processes is warranted.  相似文献   

厦门湾水体中铀、钍同位素及悬浮颗粒物的粒径谱--颗粒物采集方法的影响   总被引：2，自引：0，他引：2  

彭安国  黄奕普  陈敏  刘广山  邱雨生 《台湾海峡》2004,23(3):268-273

运用增强型混合纤雏素(CN-CA)膜、聚碳酸酯膜和聚丙烯滤芯过滤3种不同的方法采集、研究厦门湾水体中悬浮颗粒物(SPM)及其U、Th同位素的粒径谱．发现3种方法所得SPM总浓度和U、Th各同位素的总比活度具有很好的一致性,但粒级分布存在差异．SPM的浓度随粒径的增大而增加,并且SPM的粒径谱控制着颗粒活性很强的4种钍同位素的拉径谱．对于所研究的3种方法,采用聚碳酸脂膜过滤是研究沿岸海域SPM及颗粒活性核素粒级分布比较理想的方法。  相似文献   

Stable isotope and chemical composition of pearls: Biomineralization in cultured pearl oysters in ago bay, Japan     

Hodaka Kawahata  Mayuri Inoue  Masato Nohara  Atsushi Suzuki 《Journal of Oceanography》2006,62(4):405-412

The δ¹⁸O, δ¹³C and trace element composition of pearls collected from Ago Bay, Japan, were investigated in order to evaluate biomineralization in the cultured pearl oyster (Pinctada fucata martensii). The oxygen isotopic data suggest that the pearls were produced around 23–24°C, mainly in June to early July, which is consistent with their occurrence in the field. Therefore the pearls were produced under or close to isotopic equilibrium conditions, although they showed high calcification rates (higher than 0.2–1.0 g cm^{− 2}yr⁻¹) under which, for example, coral skeletons (calcification rate ∼0.28 g cm^{− 2}yr⁻¹) often show non-equilibrium isotope partitioning. The δ¹³C values were ∼− 2.9‰ lower than those calculated for offshore waters under equilibrium conditions. This may be due to low-δ¹³C bottom waters resulting from the degradation of organic matter (OM) or to a contribution of low-δ ¹³C food. In the latter case, a simple mass balance calculation gives a respiration component of 14%. Twelve trace elements of bulk pearl samples were classified into four groups on the basis of their enrichment/depletion patterns relative to seawater and inter-element relationships: group 1, Co, Cr, Pb; group 2, Ba, Cs, U; group 3, Cu, Sn, V, and group 4, Mn, Rb, Mo. Comparison with coral skeletons suggests that Ba and Mn (groups 2 and 4) were definitely much enriched in proteinaceous OM relative to aragonite crystals in pearls and that V (group 3) in pearls showed only slight enrichment in the organicrich layer. By contrast, the other elements showed small differences between both layers (enrichment factor of <3), suggesting that these elements occur largely in aragonite crystals.  相似文献   

冲绳海槽Jade热液区块状硫化物中流体包裹体的氦、氖、氩同位素组成   总被引：3，自引：1，他引：3       下载免费PDF全文

曾志刚  秦蕴珊  翟世奎 《海洋学报》2003,25(4):36-42

对冲绳海槽Jade热液区块状硫化物中流体包裹体的氦、氖和氩同位素组成进行了测定,流体包裹体的3He/4He比值为(6.2～10.1)Ra,均值为7.8Ra,与大洋中脊玄武岩一致[3He/4He≈(6～11)Ra],20Ne/22Ne比值为10.7～11.3,明显高于大气值(9.8),而40Ar/36Ar比值的变化范围在287～334之间,接近大气值(295.5),这些结果表明,块状硫化物中热液流体捕获的稀有气体是地幔和海水源组分混合的产物,且流体包裹体中的氦主要来自地幔,氖和氩主要来自海水。  相似文献   

Distribution and sources of organic carbon, nitrogen and their isotopes in sediments of the subtropical Pearl River estuary and adjacent shelf, Southern China   总被引：17，自引：1，他引：17  

Jianfang Hu  Ping'an Peng  Guodong Jia  Bixian Mai  Gan Zhang 《Marine Chemistry》2006,98(2-4):274-285

The isotopic composition (δ¹³C and δ¹⁵N) and organic carbon (OC) and total nitrogen (TN, organic plus inorganic) content of 37 carbonate-free surficial sediments of the subtropical Pearl River estuary and the adjacent shelf of South China Sea (SCS) was determined. The δ¹³C values indicate that the sediment organic material is a mixture from two sources, terrestrial and marine. Several of the sediments have extremely low (< 4) OC / TN ratios, which could be due to low OC contents and/or to a significant fraction of the TN present as inorganic nitrogen adsorbed on clays. In general, the spatial patterns of OC, TN, δ¹³C and δ¹⁵N are similar. Values are low at the river mouth and on the western coast, suggesting proportionally greater accumulation of terrestrial particulate organic matter relative to marine phytodetritus, which is limited by low productivity in the turbid plume of the Pearl River. Algal-derived organic carbon (al-OC) content is estimated to be low (≤ 0.06%) at the river mouth and higher (up to 0.57%) on the adjacent inner shelf based on a mixing model of end members.  相似文献   

Isotopic signatures of organic matter in sediments of the continental shelf facing the Orinoco Delta: Possible contribution of organic carbon from savannas     

Ernesto Medina  Marta Francisco  Leonel Sternberg  William T. Anderson 《Estuarine, Coastal and Shelf Science》2005,63(4):527-536

The ⁸⁷Sr, ¹³C, and ¹⁵N isotopic signatures of organic matter in sediments from the continental shelf facing the Orinoco Delta were measured to determine the contribution of sediments transported from the Amazon River by the coastal Guayana current and the sediments transported by the Orinoco River. Box core samples between 60 and 300 m water depth collected along 4 transects located eastwards to the Orinoco Delta were analyzed. Carbon and nitrogen concentrations decreased with depth under water on the shelf, and were strongly correlated indicating homogeneity of organic matter composition. Phosphorus content was also associated to organic matter in most samples, but some of them revealed deposition of P-enriched sediments. The ⁸⁷Sr/⁸⁶Sr ratios showed a strong continental signature averaging 0.7117, therefore, limiting the possible carbon and nitrogen sources associated with these sediments to C3 trees, C4 grasses, or freshwater phytoplankton. The δ¹³C values were relatively high averaging −21‰, above values reported for sediments on the Amapá shelf and the Amazon River in Brazil. Average δ¹³C values did not differ significantly among transects. High δ¹³C values point to the influence of organic matter transported from the C4-plants dominated savannas in the northern fringe of the Orinoco River. δ¹⁵N values were positive and averaged 5‰, being within the range of values measured in the Marajo island (Amazon River) and the estuary of the Pará River. The δ¹⁵N values differed significantly among transects (4.9–5.2‰), lowest values corresponding to the northernmost transect near the coast of Trinidad, and the highest values corresponding to the transect located at the southernmost position.  相似文献