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1.
金属硫化物Re-Os等时线年龄的合理解释是揭示金属矿床成矿时代的关键.通过对新疆东天山梅岭铜矿床开展Re-Os同位素定年研究,结果表明浸染状和脉状矿石中黄铁矿样品在Os浓度和Os同位素比值方面都有很大的变化,这两类样品定义了很好的Re-Os等时线年龄,分别为523±59 Ma和707±99 Ma.由于得到的等时线年龄明显老于它们的实际地质成矿年龄,且187Os/188Os与普通Os的倒数（以1/192Os为例）之间存在着很好的相关性（R2分别为0.997 3和0.994 5）,因此这些样品存在着初始Os同位素组成不均一的现象,这些Re-Os等时线是混合等时线,没有地质意义.理论和数学公式推导显示观测到的Re-Os等时相关性是在形成时期没有达到完全的同位素平衡的二元混合的结果,这种同位素扩散不平衡产生的原因主要是在矿床形成时期Os同位素在金属硫化物与硅酸盐矿物之间的同位素扩散存在限制性.回归得到的Os的初始值更偏向于地壳值,表明矿床形成时期的地壳混染可能造成金属硫化物体系中的这种初始Os同位素不均一.因此,将Re-Os同位素体系应用于金属硫化物样品定年时,187Os/188Os与1/192Os之间是否存在相关关系可以作为Re-Os等时线年龄是否具有地质意义的判断标准. 相似文献
2.
Preparation and Certification of Re-Os Dating Reference Materials: Molybdenites HLP and JDC 总被引：27，自引：1，他引：27
Andao Du Shuqi Wu Dezhong Sun Shuxian Wang Wenjun Qu Richard Markey Holly Stain John Morgan Dmitry Malinovskiy 《Geostandards and Geoanalytical Research》2004,28(1):41-52
Two Re-Os dating reference material molybdenites were prepared. Molybdenite JDC and molybdenite HLP are from a carbonate vein-type molybdenum-(lead)-uranium deposit in the Jinduicheng-Huanglongpu area of Shaanxi province, China. The samples proved to be homogeneous, based on the coefficient of variation of analytical results and an analysis of variance test. The sampling weight was 0.1 g for JDC and 0.025 g for HLP. An isotope dilution method was used for the determination of Re and Os. Sample decomposition and pre-concentration of Re and Os prior to measurement were accomplished using a variety of methods: acid digestion, alkali fusion, ion exchange and solvent extraction. Negative thermal ionisation mass spectrometry and inductively coupled plasma-mass spectrometry were used for the determination of Re and 187 Os concentration and isotope ratios. The certified values include the contents of Re and Os and the model ages. For HLP, the Re content was 283.8 ± 6.2 μg g−1 , 187 Os was 659 ± 14 ng g−1 and the Re-Os model age was 221.4 ± 5.6 Ma. For JDC, the Re content was 17.39 ± 0.32 μg g−1 , 187 Os was 25.46 ± 0.60 ng g−1 and the Re-Os model age was 139.6 ± 3.8 Ma. Uncertainties for both certified reference materials are stated at the 95% level of confidence. Three laboratories (from three countries: PR. China, USA, Sweden) joined in the certification programme. These certified reference materials are primarily useful for Re-Os dating of molybdenite, sulfides, black shale, etc. 相似文献
3.
A suite of 14 diamond-bearing and 3 diamond-free eclogite xenoliths from the Newlands kimberlite, South Africa, have been studied using the Re–Os isotopic system to provide constraints on the age and possible protoliths of eclogites and diamonds. Re concentrations in diamond-bearing eclogites are variable (0.03–1.34 ppb), while Os concentrations show a much more limited range (0.26–0.59 ppb). The three diamond-free eclogites have Re and Os concentrations that are at the extremes of the range of their diamond-bearing counterparts. 187Os/188Os ranges from 0.1579 to 1.4877, while 187Re/188Os varies from 0.54 to 26.2 in the diamond-bearing eclogites. The highly radiogenic Os in the diamond-bearing eclogites (γOs=23–1056) is consistent with their high 187Re/188Os and requires long-term isolation from the convecting mantle. Re–Os model ages for 9 out of 14 diamond-bearing samples lie between 3.08 and 4.54 Ga, in agreement with FTIR spectra of Newlands diamonds that show nitrogen aggregation states consistent with diamond formation in the Archean. Re–Os isochron systematics for the Newlands samples do not define a precise isochron relationship, but lines drawn between subsets of the data provide ages ranging from 2.9 to 4.1 Ga, all of which are suggestive of formation in the Archean. The Re–Os systematics combined with mineral chemistry and stable isotopic composition of the diamond-bearing eclogites are consistent with a protolith that has interacted with surficial environments. Therefore, the favored model for the origin of the Newlands diamond-bearing eclogites is via subduction. The most likely precursors for the Kaapvaal eclogites include komatiitic ocean ridge products or primitive portions of oceanic plateaus or ocean islands. 相似文献
4.
Re-Os同位素定年对岩浆型Cu-Ni硫化物矿床成矿时代的制约 总被引：3，自引：1，他引：2
Re-Os同位素体系被认为是岩浆Cu-Ni硫化物矿床直接定年的有力工具。通过研究世界级典型岩浆Cu-Ni硫化物矿床的Re-Os等时线表面年龄,发现有时能得到成矿年龄,有时得到与成矿年龄不一致的表面年龄或根本得不到Re-Os等时线,还有时同一矿床的不同类型矿石给出不同的Re-Os等时线表面年龄。文章介绍了能够解释上述现象的理论模型。模型预测对与基性-超基性岩共生的Cu-Ni硫化物矿床,除一些特殊情况外,块状矿石可得到有地质意义的Re-Os等时线年龄,浸染状矿石常得到没有地质意义的假等时线;而浸染状矿石常得到有地质意义的Os同位素初始比值,而块状矿石给出的"Os同位素表面初始比值"往往没有地质意义。因此,建议在应用Re-Os同位素体系定年时要结合矿床类型、矿石类型以及成矿过程等因素综合考虑;对Re-Os数据的科学合理解释同样需要从矿床学和同位素地球化学的基本原理出发,结合矿床的实际情况,进行深入分析研究。 相似文献
5.
Re-Os isotopes were used to constrain the source of the ore-forming elements of the Tharsis and Rio Tinto mines of the Iberian
Pyrite Belt, and the timing of mineralization. The pyrite from both mines has simila]r Os and Re concentrations, ranging between
0.05–0.7 and 0.6–66 ppb, respectively. 187Re/188Os ratios range from about 14 to 5161. Pyrite-rich ore samples from the massive ore of Tharsis and two samples of stockwork
ore from Rio Tinto yield an isochron with an age of 346 ± 26 Ma, and an initial 187Os/188Os ratio of about 0.69. Five samples from Tharsis yield an age of 353 ± 44 Ma with an initial 187Os/188Os ratio of about 0.37. A sample of massive sulfide ore from Tharsis and one from Rio Tinto lie well above both isochrons
and could represent Re mobilization after mineralization. The pyrite Re-Os ages agree with the paleontological age of 350 Ma
of the black shales in which the ores are disseminated. Our data do not permit us to determine whether the Re-Os isochron
yields the original age of ore deposition or the age of the Hercynian metamorphism that affected the ores. However, the reasonable
Re-Os age reported here indicates that the complex history of the ores that occurred after the severe metamorphic event that
affected the Iberian Pyrite Belt massive sulfide deposits did not fundamentally disturb the Re-Os geochronologic system. The
highly radiogenic initial Os isotopic ratio agrees with previous Pb isotopic studies. If the initial ratio is recording the
initial and not the metamorphic conditions, then the data indicate that the source of the metals was largely crustal. The
continental margin sediments that underlie the deposits (phyllite-quartzite group) or the volcanic rocks (volcanogenic-sedimentary
complex) in which the ores occur are plausible sources for the ore-forming metals and should constrain the models for the
genesis of these deposits.
Received: 15 March 1999 / Accepted: 26 July 1999 相似文献
6.
Rhenium-Osmium (Re-Os) isotopic dating applied to the geochronology of hydrocarbon accumulation has been the forefront of international research in the last 10 years and has achieved significant achievements. However, our current researches are lacking in Re-Os isotopic chronology on the geochronology of hydrocarbon accumulation. The successful application of the Re-Os geochronology has enabled the determination of accurate and precise depositional ages for Organic-Rich Sedimentary rocks (ORS), the establishment of timing constraints of oil generation or migration, and the fingerprinting of the source of oil. On the basis of literatures study both at home and abroad, this article mainly dealt with the principle of Re-Os isotopic dating and analyzed the accumulation processes of Re and Os in a seawater-sediment system. Meanwhile, the test samples, sample preparation and analytical methodology of Re-Os isotopic dating were summarized. The results revealed that the initial 187Os/188Os ratio could constrain the age of oil generation or migration, and effectively evaluated the relationship between source rock and oil. The radiogenic 187Os/188Os ratio showed a positively correlated relationship with source rock age. This article proposed that hydrocarbon mature, biodegradation and water washing had minimal or no effect on data scatter about Re-Os isochron. However, the effects of postdepositional mobility of Re and Os, variations in the initial 187Os/188Os ratio, and thermochemical sulfate reduction could result in data scatter. The reproducibility and accuracy of Re-Os age was also closely related to the sample particle size and sample amount. Compared with other isotopic dating, the biggest advantage of Re-Os isotopic dating is to study geological body related to accumulation process, and to obtain direct evidence of hydrocarbon accumulation period. From what was discussed above, the article discussed the existing problems and put forward the future hot research and development direction of Re-Os isotope system, so as to promote the deep development of relative theory and technology of Re-Os isotopic dating. 相似文献
7.
Re-Os Age of Cu-Ni Ores from the Huangshandong Cu-Ni Sulfide Deposit in the East Tianshan Mountains and Its Implication for Geodynamic Processes 总被引：4，自引：0，他引：4
MAO Jingwen YANG Jianmin QU Wenjun DU Andao WANG Zhiliang HAN Chunming Faculty of Geosciences Resources China University of Geosciences Beijing E-mail: jingwenmao@.netInstitute of Mineral Resources Chinese Academy of Geological Sciences Beijing National Research Center of Geoanalysis Chinese Academy of Geological Sciences Beijing 《《地质学报》英文版》2003,77(2):220-226
An isochron age of 282±20 (95% conf. limit) Ma of the sulfide ores in the Huangshandong Cu-Ni sulfide deposit, the East Tianshan Mountains has been obtained through Re-Os isotopic measurement. The age implies that the Cu-Ni sulfide deposit and other related deposits in the same area occurred in a Permian extensional environment of post-collision instead of Devonian-Early Carboniferous ophiolite-related oceanic or island arc environments inferred before. It shares the same ages with the orogenic and epithermal gold deposit systems in the same area. An initial 187Os/188Os ratio of 0.25±0.04 (1σ) and a γos value of 99 on average display the participation of large quantities of crustal components into the rock-forming and ore-forming system during mineralization and magmatic emplacement. 相似文献
8.
The geochemistry of Re-Os and the recent use of Re as a non-traditional stable isotope both need accurate and precise quantification of 187 Re/185 Re ratios. This paper reports rhenium isotopic data obtained from the analysis of a standard solution and geological samples by MC-ICP-MS. We show that measured isotopic ratios are modified by matrix effects that cannot be accounted for by the standard solution bracketing technique. The bias resulting from measurements on a spiked (185 Re-enriched) sample is shown to alter the apparent Re concentration by several percent. When spiking samples and calibrators with tungsten, simultaneous measurement of tungsten and rhenium isotopes compensates for the matrix-induced modification of mass bias. Rhenium and tungsten are shown to have different fractionation factors. This may be due to the fact that the two elements fractionate in a different but systematic way, or that the reference isotopic ratios used for elemental Re and W are incoherent with one another. The consistency of fractionation through time can be used to obtain an empirical relationship between W and Re measured ratios from a standard solution to obtain a sample's fractionation-corrected 187 Re/185 Re spiked ratio on samples containing pg g−1 levels of Re, even if some matrix capable of affecting mass bias remains in the final solution. 相似文献
9.
新疆坡北基性-超基性岩带10号岩体SHRIMP U-Pb和矿石Re-Os同位素定年及其意义 总被引：9，自引：2，他引：7
坡北基性-超基性岩带10号岩体位于塔里木板块东北部北山裂谷带内,岩体侵位于下石炭统红柳园组.前人根据岩体侵位地层的时代,间接推断出该岩体形成年龄为晚石炭世一早二叠世.文章对坡北基性-超基性岩带的10号岩体辉长岩和浸染状矿石分别进行了锆石SHRIMP U-Pb、Re-Os定年和Sr-Nd同位素示踪研究,获得岩体的辉长岩锆石SHRIMP U-Pb年龄信息比较分散,其表面年龄信息从古生代-新元古代-古元古代-新太古代均有显示,揭示了新疆塔里木板块东北部北山裂谷带内的基性-超基性岩体的形成经历了复杂的地质演化历史.所获得的主体锆石的年龄为(289±13)Ma(95%可信度),与岩体侵位于下石炭统红柳园组的地质事实相吻合,可能代表了岩体形成的时间,而年龄信息(2 559～2 589 Ma)暗示了北山地区可能存在古元古代一新太古代的结晶基底.获得浸染状铜镍硫化物矿石的Re-Os等时线年龄为(413±20)Ma(95%可信度),该年龄不仅大于含矿超基性岩体(289 Ma)的形成时代,而且也老于岩体所侵入的下石炭统红柳园组的地层时代,显然与宏观的地质证据相悖.Sr-Nd和Os同位素特征研究表明,坡北岩带在约280 Ma前成岩成矿时,岩浆在从地幔源区侵入到地壳过程中受到了地壳物质混染,致使浸染状矿石的Re-Os同位素体系呈二元混合体系,因此浸染状矿石Re-Os同位素体系确定的等时线疑为假等时线,其年龄不能代表矿床形成时代或不具有确切的地质意义.铜镍矿化无论从时间上还是空间上都与岩体的侵位密切相关,矿床成因类型又为岩浆熔离型矿床,表明坡北10号铜镍硫化物矿床的成岩成矿时间应发生在晚石炭世一早二叠世期间,是后碰撞构造背景下幔源岩浆上侵的产物. 相似文献
10.
Tarun K. Dalai Katsuhiko Suzuki Masao Minagawa Yoshiyuki Nozaki 《Chemical Geology》2005,220(3-4):303-314
Concentrations of Re and Os, and the isotopic composition of Os have been measured in the Japan Sea sediments to assess the response of the Japan Sea to glacial–interglacial climate change and associated weathering fluxes. The osmium concentrations in the sediment samples analyzed vary from 59 to 371 pg/g, and 187Os/188Os from 0.935 to 1.042. Only 187Os/188Os of sediment samples from dark laminations deposited under suboxic to anoxic conditions and having elevated concentrations of Re and Os, and with ≥ 80% hydrogenous Os are explained in terms of seawater composition. Lower 187Os/188Os were observed for sediments deposited during the last glacial maximum (LGM) when planktonic foraminifera from the Japan Sea recorded lighter oxygen isotopic composition. Decrease in dissolved Os fluxes from continents and/or change in the composition of the dissolved load to the Japan Sea are suggested as the driving mechanisms for the observed lower LGM 187Os/188Os. The results of this study, coupled with lower 187Os/188Os during the last glacial observed at other sites from ocean basins with different lithology and contrasting sediment accumulation rates, suggest that this trend is characteristic of the global oceans.
Data from this study show that the Japan Sea recorded higher 187Os/188Os during the current interglacial coinciding with excursions of oxygen isotopic compositions of planktonic foraminifera to heavier values. This is explained in terms of preferential release of 187Os during deglacial weathering and/or higher continental Os flux driven by warm and wet climate. This study demonstrates that Os isotopic composition of reducing margin sediments has immense potential to track variations in the seawater composition. In addition, 187Os/188Os of reducing sediments may be used to draw inferences about local paleoceanographic processes in semi-enclosed basins such as the Japan Sea. 相似文献
11.
赤柏松岩浆型铜镍硫化物矿床位于华北克拉通胶辽吉带,含矿镁铁质—超镁铁质岩侵入到鞍山群最下部的四道砬子河组变质岩中;该矿床硫化物矿样品的Os和Re浓度分别为19×10-3~490×10-3和0.47×10-3~13.97×10-3,对这些数据分析得出了一条6点Re-Os等时线年龄为1 885±94 Ma,矿石的初始(187)^Os/(188)^Os 比值为0.80±0.16 (MSWD=0.17),表明矿石为岩浆源,熔体主要由地幔贡献,但在成矿过程及岩浆侵位期间有不少地壳物质混入成岩成矿系统。新的Re-Os年代学结果表明,赤柏松镁铁质—超镁铁质侵入体与铜镍矿床形成于古元古代,而不是前人认为的早白垩世。 相似文献
12.
对流上地幔Os同位素组成的准确估算是运用Re-Os同位素体系探讨地幔演化的基础。前人研究主要是以地幔橄榄岩为研究对象,由于地幔橄榄岩Os同位素存在明显的不均一性,因而直接影响估算值的准确性。对流上地幔中包含的不同亏损程度的难熔组分在部分熔融过程中难以熔融,对形成的熔体相的Os同位素组成贡献很少或者没有。因此,与对流上地幔具有相同的Os同位素组成初始值的早期分离结晶岩石(如堆晶岩),结合堆晶岩中锆石的准确定年,可以用来估算对流上地幔Os同位素组成。本文根据这一方法测试了那曲地区弧后盆地堆晶岩的Os同位素组成和锆石U-Pb年龄,推测那曲地区新特提斯洋对流上地幔Os同位素组成为碳质球粒陨石型的。根据这一模型,对比了罗布莎和东巧铬铁矿岩、含矿围岩以及不含矿围岩的Os同位素特征,揭示出矿石及围岩均具有古老大陆岩石圈地幔信息,而不含矿围岩(泽当岩体)的Os同位素组成为碳质球粒陨石型的,无古老大陆岩石圈地幔信息。 相似文献
13.
新疆哈密月牙湾铜镍矿是近年来在东天山卡拉塔格地区新发现的岩浆型铜镍硫化物矿床.为确定该矿床的成岩、成矿时代及其成矿作用,利用锆石LA-ICP-MS U-Pb定年和硫化物Re-Os同位素等时线定年方法,分别对主含矿岩相橄榄辉长岩和矿石中的磁黄铁矿进行了年龄测定.橄榄辉长岩中锆石的206Pb/238U年龄为255~292 Ma,加权平均值为274±2.4 Ma,代表了橄榄辉长岩的成岩年龄;矿石中磁黄铁矿Re-Os同位素等时线年龄为271.9±9.5 Ma,代表了硫化物熔离成矿的年龄;187Os/188Os初始值为0.279 6±0.008 9,γOs值为117~126,指示在岩浆侵位及硫化物熔离成矿过程中有地壳物质加入.月牙湾镁铁质岩浆的成岩、成矿作用发生于早二叠世,与东天山黄山-图拉尔根一带典型铜镍硫化物矿床为同一时期的产物. 相似文献
14.
Proterozoic melting in the northern peridotite Massif, Zabargad Island: Os isotopic evidence 总被引：1，自引：0，他引：1
The geodynamic history of the three Zabargad peridotite bodies is the key to their significance as samples of the upper mantle. Currently, there are two main hypotheses that differ greatly in their implications for the origin and age of the peridotite complex as a whole. In the first, the Zabargad peridotite bodies all represent young asthenospheric mantle that was juxtaposed with ancient crustal gneisses during the opening of the Red Sea. In the second, the complex may represent a single package of residual mantle and lower crust of Pan-African age that was uplifted during the Miocene. In order to distinguish between these two models, we have analysed five samples of Zabargad peridotite and two pyroxenites for Os isotopes. The 187 Os/188 Os results range from 0.1198 to 0.1320 and correlate with Al2 O3 , allowing an age inference for the northern body, based on the Os isotopic evolution curve for the bulk Earth, of 1.4±0.3 Gyr. This is at least as old as the previously inferred Pan-African age and may be older, and agrees with previous suggestions that the northern and central peridotite bodies probably represent ancient continental lithospheric mantle, while the southern body represents recent asthenospheric mantle. Our results from both central and southern bodies are consistent with either crustal age hypothesis. 相似文献
15.
A double spike for osmium analysis of highly radiogenic samples 总被引：1，自引：0，他引：1
Richard Markey Judith L. Hannah John W. Morgan Holly J. Stein 《Chemical Geology》2003,200(3-4):395-406
Geologic samples containing highly radiogenic Os (molybdenites and low-level, highly radiogenic (LLHR) samples) have no internal means by which to correct for mass fractionation during isotopic measurement by mass spectrometry. We describe a double spike for use with highly radiogenic samples, created by combining isotopically enriched 188Os and 190Os. Spiking molybdenite and other highly radiogenic minerals with this tracer allows for a fractionation correction, as well as a more reliable determination of common Os relative to analysis using single spikes.
The precise isotopic composition of the double spike is determined by a calibration against natural Os, in which two separate measurements are necessary: one each for the pure double spike and the spike–standard mixture. An estimate of the true composition of the spike is obtained by least squares approximation, and the errors are obtained by Monte Carlo methods. Sample analyses are then much more straightforward than the calibration because isotopic compositions of all components are known a priori.
Results obtained with a mixed Re-double Os spike demonstrate an improved reproducibility over individual 185Re and 190Os spikes. For an Archean in-house molybdenite standard we now observe a reproducibility of 0.08%. The ability to make a fractionation correction is essential for Os measurements made by ion counting. With the double Os spike, young samples and those with low Re contents (i.e., LLHR) can now be accurately analyzed. The 188Os–190Os double spike also allows a determination of the common Os contents of highly radiogenic samples. Common Os is poorly determined for ancient samples with high concentrations of 187Os, which fortunately are not sensitive to estimates of common Os. Common Os can be reasonably well determined for younger samples and those with low Re contents. We report a common Os concentration of 0.4±0.1 ppb for an 11 Ma molybdenite. Consideration of common Os content is important for age determination of young samples and LLHR samples, and is not possible by other published means of Os analysis. 相似文献
16.
The Tudun deposit is a medium-sized Cu–Ni sulfide deposit, located at the westernmost edge of the Huangshan–Jing’erquan Belt in the northern part of Eastern Tianshan, NW China. Sulfide separates including pentlandite, pyrrhotite and chalcopyrite from the Tudun deposit, contain Re, common Os and 187Os ranging from 40.46 to 201.2, 0.8048 to 6.246 and 0.1709 to 0.9977 ppb, respectively. They have very low 187Os/188Os ratios of 1.224–2.352. The sulfides yield a Re–Os isochron age of 270.0 ± 7.5 Ma (MSWD = 1.3), consistent within uncertainty with the SHRIMP zircon U–Pb age for the Tudun mafic intrusion (gabbro) of 280.0 ± 3.0 Ma. The calculated initial 187Os/188Os ratio is 0.533 ± 0.022, and γOs values range from 283 to 307, with a mean of 297, indicating significant crustal contamination of the parent melt prior to sulfide saturation. The Tudun deposit shares the same age and Re–Os isotopic compositions with other orthomagmatic Cu–Ni sulfide deposits in Huangshan–Jing’erquan Belt, suggesting that they have formed in Early Permian. 相似文献
17.
湖南鲁塘石墨矿Re-Os同位素研究 总被引：5，自引：1，他引：4
石墨具有较高的Re、Os含量,可望成为理想的Re-Os同位素测年对象,但迄今国内外研究较少,尤其在煤层经变质作用形成石墨过程中,其中Re-Os同位素体系的变化还有待研究。湖南鲁塘石墨矿是我国典型的隐晶质石墨矿床之一,矿体产于二叠系龙潭组煤系地层中。本文采用Carius管逆王水溶解样品,直接蒸馏、微蒸馏分离纯化Os,丙酮萃取法分离富集Re,热表面电离质谱法对鲁塘矿区石墨样品以及外围原煤进行了Re-Os同位素分析。结果表明:鲁塘石墨的Re含量为0.901~9.794 ng/g,Os含量为7.3~189.5 pg/g,Re-Os同位素等时线年龄为155.6±3.6 Ma,该年龄与鲁塘石墨矿东侧骑田岭岩体第二阶段中粒黑云母花岗岩锆石U-Pb年龄153~157 Ma一致,表明了龙潭组煤层受到骑田岭岩体"烘烤"作用,发生热接触变质作用,使得靠近骑田岭岩体原煤变质为石墨,形成石墨矿床。通过对比石墨、原煤和骑田岭岩体Re、Os含量及比值,发现石墨中的Re、Os主要来源于原煤,并根据石墨Re-Os等时线初始(187Os/188Os)i值(0.686±0.032),推测骑田岭岩体在侵入煤系地层过程中,有少量具有较低187Os/188Os值的Os被碳质吸附。 相似文献
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黑矿型矿床成矿物质来源：日本上向黑矿铼—锇和氦同位素证据 总被引：5，自引：1，他引：5
上向黑矿（Uwamuki Kuroko)是日本最典型的黑矿型矿床，它形成于日本岛弧中新世矢折岛弧裂谷环境，产于双峰式岩石组合的长英质火山岩系中。矿床由下部筒状硅矿带和上部块状黑矿带构成，后者显示典型的上黑（黑矿）下黄（黄矿）金属分带。为探索研究长期争议的成矿物质来源，系统测定了矿石和主岩的Os,He同位素组成。含矿流纹岩系的R／RA值介于0．93－1．14间，证实该岩浆可能主要来源于陆壳重熔。上向黑矿的上部块状黑矿矿石具较高的^187Os/^188Os值（2．246－7．608），反映矿石Os主体来源于壳源沉积物或矿区基底岩系；下部脉状－网脉状硅矿、块状黄矿和少量黑矿则具低^187Os/^188Os值（0．423－0．793），证实矿石Os具两源性，估计幔源物质贡献约57％－89％，壳源物质贡献约11％－43％。此外，在上部块状黑矿带内部，矿石 ^187Os/^188O显示清楚的垂向韵律性变化，揭示了成矿流体及成矿物质的周期性混合，据此，本文提出了一个新的两阶段成矿模式。 相似文献
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滇东南八布地区发育一套晚古生代超镁铁质-镁铁质杂岩,是认识古特提斯分支洋构造演化的重要窗口,而其中以火山岩为赋矿围岩的杨万铜矿床,被视作区域找矿的突破点。目前,对这套超镁铁质-镁铁质杂岩的构造属性及赋存铜矿床的成矿时代及成因联系还存在争议。通过对杨万铜矿床中黄铜矿和黄铁矿进行Re-Os同位素定年,获得Re-Os等时线年龄为269±3 Ma,表明该矿床形成于早中二叠世,与火山岩(～270 Ma)大致同时;而初始187Os/188Os值为0.31±0.17,暗示成矿时存在热液流体与古海水的相互作用。区内玄武岩围岩和其它超镁铁质-镁铁质岩石的地球化学特征对比分析显示,八布超镁铁质-镁铁质杂岩为一套N-MORB型蛇绿岩组合,代表了古特提斯分支洋盆的洋壳残片。杨万铜矿床应划归为与古特提斯分支洋裂解有关的火山成因块状硫化物(VMS)矿床,其周边地区具有较好的找矿潜力。 相似文献