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1.
Re-Os study of Fe-Ti-V oxide and Fe-Cu-Ni sulfide deposits, Suwałki Anorthosite Massif, northeast Poland 总被引：1，自引：0，他引：1
J. W. Morgan H. J. Stein J. L. Hannah R. J. Markey J. Wiszniewska 《Mineralium Deposita》2000,35(5):391-401
The Suwałki anorthosite massif, located in extreme northeast Poland beneath more than a kilometer of Phanerozoic cover, hosts
major Fe-Ti-V deposits. These deposits, discovered in 1962, are contained in Fe and Ti oxide minerals that coexist with subordinate
quantities of Fe, Cu, Ni, and Co sulfides in massif-style anorthosites, norites, and gabbronorites. Accessibility and other
considerations preclude development of this natural resource in the present economic climate. Detailed work by Polish geologists
during the last 35 years provides a sound geologic framework for this Re-Os study of the age and origin of oxide and sulfide
deposits associated with a major, but lesser known anorthosite massif. Rhenium and osmium abundances and Os isotopic compositions
were measured for nine sulfides and four titanomagnetites from the Suwałki anorthosite massif. The titanomagnetites are over
an order of magnitude lower in Re (0.4–1.5 ppb) and Os (0.036–0.144 ppb) concentrations than co-precipitated pyrrhotite, pyrite,
and chalcopyrite that yield consistent concentrations for Re (30–55 ppb) and Os (1–6 ppb). Parallel lines connecting co-existing
titanomagnetite and sulfides have slopes of ∼1 on Re versus common Os concentration plots, indicating that both Re and Os
behave similarly during crystallization in their high preference for any sulfide phase over magnetite. Samples from three
deposits within the anorthosite massif were analyzed. An age of 1559 ± 37 Ma (n=10) with an initial 187Os/188Os of 1.16 ± 0.06 for the Jezioro Okrągłe and Krzemianka deposits is essentially identical to an age of 1556 ± 94 Ma (n=3) for the Udryń deposit. Udryń, however, yielded a marginally lower initial 187Os/188Os of 0.87 ± 0.20. The high initial 187Os/188Os combined with the Proterozoic Re-Os age indicates that the source for Suwałki oxides-sulfides is older crust, and hypothetically,
could involve Archean rocks. An average crustal value of 50 for 187Re/188Os yields a 2777 Ma age for Suwałki source rocks. Widespread Phanerozoic cover severely limits knowledge of basement rocks
in Poland, however, and no Archean rocks are known in the immediate region. More likely, 187Re/188Os ratios may be higher than average continental crust, reflecting mafic crust in the source, and may move the source age
for Suwałki anorthosite and mineral deposits toward younger values that easily include ∼2.0 Ga Proterozoic rocks. This more
favorable case also accommodates Paleoproterozoic Nd model ages. Regardless of Archean or Proterozoic source age, the high
initial 187Os/188Os ratios derived from the Re-Os isochron indicate that the source for the oxide-sulfide mineral deposits is more likely the
crust and not the mantle. Given that these deposits are clearly magmatic, the Re-Os results add a new dimension to the long-standing
“origin of anorthosite” problem, implying a crustal source for the anorthosite as well. The 1559 Ma Suwałki age is compatible
with a well-exposed east-west band of 1530-1660 Ma rapakivi granite-anorthosite magmatism to the immediate north, transecting
western Russia, southern Finland, Estonia and Latvia, and central Sweden. In particular, the age and isotopic character of
Suwałki are not unlike those of the well-studied Salmi rapakivi granite-anorthosite batholith in western Russia (Karelia).
Received: 4 December 1998 / Accepted: 11 November 1999 相似文献
2.
Seven 187Re-187Os ages were determined for molybdenite and pyrite samples from two well-dated Precambrian intrusions in Fennoscandia to examine
the sustainability of the Re-Os chronometer in a metamorphic and metasomatic setting. Using a new 187Re decay constant (1.666 × 10−11y−1) with a much improved uncertainty (±0.31%), we determined replicate Re-Os ages for molybdenite and pyrite from the Kuittila
and Kivisuo prospects in easternmost Finland and for molybdenite from the Kabeliai prospect in southernmost Lithuania. These
two localities contain some of the oldest and youngest plutonic activity in Fennoscandia and are associated with newly discovered
economic Au mineralization (Ilomantsi, Finland) and a Cu-Mo prospect (Kabeliai, Lithuania). Two Re-Os ages for vein-hosted
Kabeliai molybdenite average 1486 ± 5 Ma, in excellent agreement with a 1505 ± 11 Ma U-Pb zircon age for the hosting Kabeliai
granite pluton. The slightly younger age suggests the introduction of Cu-Mo mineralization by a later phase of the Kabeliai
magmatic system. Mean Re-Os ages of 2778 ± 8 Ma and 2781 ± 8 Ma for Kuittila and Kivisuo molybdenites, respectively, are in
reasonable agreement with a 2753 ± 5 Ma weighted mean U-Pb zircon age for hosting Kuittila tonalite. These Re-Os ages agree
well with less precise ages of 2789 ± 290 Ma for a Rb-Sr whole-rock isochron and 2771 ± 75 Ma for the average of six Sm-Nd
TDM model ages for Kuittila tonalite. Three Re-Os analyses of a single pyrite mineral separate, from the same sample of Kuittila
pluton that yielded a molybdenite separate, provide individual model ages of 2710 ± 27, 2777 ± 28, and 2830 ± 28 Ma (Re = 17.4,
12.1, and 8.4 ppb, respectively), with a mean value of 2770 ± 120 Ma in agreement with the Kuittila molybdenite age. The Re
and 187Os abundances in these three pyrite splits are highly correlated (r = 0.9994), and provide a 187Re-187Os isochron age of 2607 ± 47 Ma with an intercept of 21 ppt 187Os (MSWD = 1.1). It appears that the Re-Os isotopic system in pyrite has been reset on the millimeter scale and that the 21 ppt 187Os intercept reflects the in situ decay of 187Re during the ∼160 to 170 m.y. interval from ∼2778 Ma (time of molybdenite ± pyrite deposition) to ∼2607 Ma (time of pyrite
resetting). When the Re-Os data for molybdenites from the nearby Kivisuo prospect are plotted together with the Kuittila molybdenite
and pyrite data, a well-constrained five-point isochron with an age of 2780 ± 8 Ma and a 187Os intercept (−2.4 ± 3.8 ppt) of essentially zero results (MSWD = 1.5). We suggest that the pyrite isochron age records a
regional metamorphic and/or hydrothermal event, possibly the time of Au mineralization. A proposed Re-Os age of ∼2607 Ma for
Au mineralization is in good agreement with radiometric ages by other methods that address the timing of Archean Au mineralization
in deposits worldwide (so-called “late Au model”). Molybdenite, in contrast, provides a robust Re-Os chronometer, retaining
its original formation age of ∼2780 Ma, despite subsequent metamorphic disturbances in Archean and Proterozoic time.
Received: 25 September 1996 / Accepted: 27 August 1997 相似文献
3.
John W. Morgan Richard J. WalkerMary F. Horan Ellyn S. BearyAnthony J. Naldrett 《Geochimica et cosmochimica acta》2002,66(2):273-290
We measured by negative thermal ionization mass spectrometry (NTIMS) Re, Os and 186Os/188Os and 187Os/188Os in 26 samples of 18 Ni-Cu sulfide ores from the Falconbridge, McCreedy West, and Strathcona mines at Sudbury, Ontario. At McCreedy West and Falconbridge, the isochron Re-Os ages are 1835 ± 70 Ma and 1827 ± 340 Ma, and the initial 187Os/188Os ratios 0.514 ± 0.019 and 0.550 ± 0.024, respectively. The ages agree with the canonical value of 1850 ± 1 Ma for the Sudbury Igneous Complex (SIC). For Hangingwall and Deep Zone ores at Strathcona, the age of 1780 ± 7 Ma may reflect resetting by dyke activity. The high initial 187Os/188Os of 0.934 ± 0.005 in these ores is distinct from those at McCreedy West and Falconbridge. Strathcona Deep Copper Zone ores have highly radiogenic Os giving a mean model age of 1883 ± 54 Ma that is similar to ages at McCreedy West and Falconbridge, but distinct from other Strathcona sulfides. Initial 186Os/188Os in two Strathcona ores with low 190Pt/188Os average 0.119 826 ± 0.000 009 (n = 3) and 0.119 827 ± 0.000 004 (n = 3), respectively, with a grand mean of 0.119 827 ± 0.000 003. This ratio may be slightly lower than the chondritic value at that time. Similar ores at Falconbridge and McCreedy West show more scatter, averaging 0.119 855 ± 0.000 008 (n = 6) and 0.119 867 ± 0.000 020 (n = 3), respectively. These values are substantially suprachondritic. The Re-Os isotope systematics of Sudbury ores are clearly of crustal origin and may be derived from a binary mixture of Superior Province and Huronian metasedimentary rocks, with Strathcona, Falconbridge, and McCreedy West ores containing, respectively, 55%, 16%, and 12% of Os from Superior sediments. The suprachondritic 186Os/188Os at McCreedy West and Falconbridge may be due to admixture of Archean or Paleozoic mafic rocks with 190Pt/188Os ≈ 0.1. No trace of the asteroid that produced the Sudbury Structure has been reported. At the Whistle mine S-poor olivine melanorite inclusions with high Ni and Os and low 187Os/188Os may contain the signature of a magmatically fractionated asteroidal core contributing 1 to 2.5 % metal. The S-poor melanorite Ni and Os data are equally well explained by admixture of ≈40% mantle peridotite, however. 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.
Shenghong Yang Wenjun Qu Yulong Tian Jiangfeng Chen Gang Yang Andao Du 《Chemical Geology》2008,247(3-4):401-418
Apparent Re–Os ages of some magmatic sulfide ore deposits are older than the zircon and baddeleyite U–Pb ages which are interpreted as the formation age of the host intrusions. The Jinchuan Ni–Cu–PGE deposit of China, the world's third largest, is such a case. We report apparent Re–Os isochron ages of 1117 ± 67 Ma, 1074 ± 120 Ma and 867 ± 75 Ma with initial 187Os/188Os ratios of 0.120 ± 0.012, 0.162 ±0.017 and 0.235 ± 0.027 for disseminated ores, sulfides from the disseminated ores and massive ores from Jinchuan, respectively. Using these data and Re–Os ages from the literature, we find that the oldest apparent Re–Os age and lowest initial Os isotope ratio are from disseminated ores which contain small amounts of sulfide minerals, the highest initial Os isotope ratios and youngest apparent Re–Os ages, consistent with the zircon and baddeleyite U–Pb ages, are from massive ores containing 90–100 modal% sulfide, and net-textured ores with about 25 modal% sulfides yield apparent Re–Os ages and initial Os ratios intermediate between those of the disseminated and massive ores.Because Os diffusion between sulfides is inhibited by the intervening silicates even at high temperatures, re-equilibration did not occur in the disseminated ore and the samples retained the Os ratios of the contaminated magma, leading to geologically meaningless ages that are older than the formation age of the rocks. While Os-bearing sulfide minerals and magnetite show low closure temperatures of Os diffusion and the sulfide minerals in the massive ore are closely connected with each other, facilitating fast diffusion of Os, re-equilibration of Os was achieved during cooling of the ore from about 850 °C after the segregation to about 400 °C. Thus, an age corresponding to the formation time and an elevated initial Os ratio were yielded by the massive ore. Os isotopes in the net-textured ore behave in the way intermediate between the disseminated and massive ores. Pb isotope data support the Os results. Disseminated ores have heterogeneous Pb isotope ratios whereas Pb in the massive ores is more uniform, consistent with Pb isotopic equilibration in the massive ores, but not in the disseminated ores. 相似文献
6.
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
7.
滇东北会泽超大型铅锌矿Re-Os同位素特征及喜山期成矿作用动力学背景探讨 总被引：2，自引：0，他引：2
会泽超大型铅锌矿是滇东北铅锌多金属成矿域中典型的密西西比河谷型(MVT)或会泽型(HZT)矿床,因其独特的成矿系统以及矿床中富锗而被地质学者熟知,由于该类型矿床成矿温度较低且缺少合适的定年矿物,其成矿时代一直存在较大的争议。本文在会泽铅锌矿麒麟厂矿区1584中段0-11号穿脉坑道块状铅锌硫化物矿石中挑选了9件硫化物样品(黄铁矿、方铅矿和闪锌矿),采用负离子热表面电离质谱法进行Re-Os同位素分析,获得Re-Os等时线年龄为40.7±2.6 Ma(n=9),与模式年龄加权平均值40.0±2.6Ma(n=8)在误差内完全一致,闪锌矿和方铅矿模式年龄分别为38.24±0.41 Ma和36.57±0.40 Ma。上述同位素年龄揭示了会泽超大型铅锌矿的成矿时代可能为始新世。结合滇东北铅锌矿集区NE向逆冲断层和冲断褶皱控矿构造区域构造解析以及断裂、矿体构造-岩相蚀变特征,提出会泽超大型铅锌矿经历了燕山期、喜山期两阶段构造-流体贯入的成矿作用模型。 相似文献
8.
Re–Os dating of disseminated ore from the Kalatongke Cu–Ni sulfide mineral deposit, Xinjiang, Northwest (NW) China, yields an apparent isochron age of 433 ± 31 Ma with an apparent initial 187Os/188Os (433 Ma) ratio of 0.197 ± 0.027. This apparent age is older than not only the zircon U–Pb age of the host intrusion (287 ± 5 Ma, Han et al., 2004) but also the stratigraphic age of the intruded country rock. Thus, the regression line is a pseudo-isochron. However, previous Re–Os dating of massive ores of the same deposit yielded an age that is consistent, within analytical uncertainty, with the zircon U–Pb age (Zhang et al., 2008). This relationship is similar to that observed in the Jinchuan deposit, NW China. Therefore, we suggested that the same mechanism, post-segregation diffusion of Os (Yang et al., 2008), is applicable to the Kalatongke deposit.Re–Os isotopic studies of Kalatongke, Jinchuan and representative magmatic Cu–Ni sulfide deposits suggest that the massive ores of mafic–ultramafic-rock-associated Cu–Ni sulfide deposits would yield geologically meaningful Re–Os age, whereas a pseudo-isochron would be obtained for the disseminated ores. Therefore, to obtain a geologically meaningful Re–Os age, the type of the deposit, the type of the ore and the ore-forming process should be taken into account. 相似文献
9.
Re-Os Dating of Sulfides from the Volcanogenic Massive Sulfide Deposit at Gacun, Southwestern China 总被引：1，自引：0，他引：1
Abstract. The Re-Os isotopic compositions of sulfide ores were analyzed for the Gacun, a volcanogenic massive sulfide deposit in southwestern China, to constrain the timing of mineralization. Sulfide ores from the deposit have a wide range of Re and Os concentrations, varying from 80.2 to 1543.2 ppb and from 0.307 to 8.83 ppb, respectively, and yielded a limited field of high 187 Re/188 Os and high 187 Os/188Os ratios, ranging from 1452 to 3309 and from 5.77 to 13.24, respectively. All sulfide samples yielded an isochron with an age of 217±28 Ma and an initial 187 Os/188 Os ratio of around 0.52±0.73. The Re-Os isochron age agrees with ages previously constrained by the other isotopic dating of the host rocks and fossil strata for the deposit. The rhythmic variation in 187 Os/188 Os and 187 Re/188 Os ratios within massive sulfide zone records a complicated process for ore-forming fluids episodically vented into the brine pool on the Mesozoic seafloor. 相似文献
10.
川西里伍式富铜矿位于扬子地台西缘和松潘-甘孜造山带接合带的江浪穹窿中。矿体大体上呈层状-似层状或透镜状。前期的矿床地质特征调查及矿相学研究结果表明,里伍铜矿的矿体至少经历了两期富集过程:早期硫化物构造变形特征明显,成典型的条带状构造,而晚期的矿化不具变形特征,主要呈块状、团块-浸染状及脉状矿构造叠加改造于前者之上。本文对里伍和中咀矿床中早期条带状黄铜矿进行了Re-Os同位素定年,获得一个良好的等时线年龄为343±11 Ma(n=4,2σ),初始~(187)Os/~(188)Os比值为~2.37。本文据此认为里伍式富铜矿早期成矿事件始于早石炭世,明显晚于赋矿围岩——元古界里伍岩群,该时期的成矿物质主要来源于大陆上地壳。 相似文献
11.
Osmium isotopic compositions, and Re and Os concentrations have been examined in one komatiite unit and two komatiitic basalt units at Dundonald Beach, part of the 2.7 Ga Kidd-Munro volcanic assemblage in the Abitibi greenstone belt, Ontario, Canada. The komatiitic rocks in this locality record at least three episodes of alteration of Re-Os elemental and isotope systematics. First, an average of 40% and as much as 75% Re may have been lost due to shallow degassing during eruption and/or hydrothermal leaching during or immediately after emplacement. Second, the Re-Os isotope systematics of whole rock samples with 187Re/188Os ratios >1 were reset at ∼2.5 Ga, possibly due to a regional metamorphic event. Third, there is evidence for relatively recent gain and loss of Re in some rocks.Despite the open-system behavior, some aspects of the Re-Os systematics of these rocks can be deciphered. The bulk distribution coefficient for Os (DOssolid/liquid) for the Dundonald rocks is ∼3 ± 1 and is well within the estimated D values obtained for komatiites from the nearby Alexo area and stratigraphically-equivalent komatiites from Munro Township. This suggests that Os was moderately compatible during crystal-liquid fractionation of the magmas parental to the Kidd-Munro komatiitic rocks. Whole-rock samples and chromite separates with low 187Re/188Os ratios (<1) yield a precise chondritic average initial 187Os/188Os ratio of 0.1083 ± 0.0006 (γOs = 0.0 ± 0.6) for their well-constrained ∼2715 Ma crystallization age. The chondritic initial Os isotopic composition of the mantle source for the Dundonald rocks is consistent with that determined for komatiites in the Alexo area and in Munro Township, suggesting that the mantle source region for the Kidd-Munro volcanic assemblage had evolved with a long-term chondritic Re/Os before eruption. The chondritic initial Os isotopic composition of the Kidd-Munro komatiites is indistinguishable from that of the projected contemporaneous convective upper mantle. The uniform chondritic Os isotopic composition of the Kidd-Munro komatiites contrasts with the typical large-scale Os isotopic heterogeneity in the mantle sources for ca. 89 Ma komatiites from the Gorgona Island, arc-related rocks and present-day ocean island basalts. This suggests that the Kidd-Munro komatiites sampled a late-Archean mantle source region that was significantly more homogeneous with respect to Re/Os relative to most modern mantle-derived rocks. 相似文献
12.
13.
石墨Re-Os同位素分析及其在成矿年代学中的初步运用 总被引：4，自引：0，他引：4
本文探索性地对江西省铅山县长寿源铅锌共生的晶质石墨进行了Re-Os同位素分析。研究结果显示石墨的Re-Os同位素年龄为424±25Ma(n=7,MSWD=7.8),与该区二云二长花岗岩中锆石的年龄(433±9Ma)在误差范围内相一致,说明石墨的成因与区域上岩浆的侵入存在密切联系。Re的含量介于47×10-9～330×10-9之间,普通Os和187Os的含量分别为0.32×10-9～2.15×10-9和0.27×10-9～1.75×10-9,相对于Re、Os在地壳中的丰度显著富集,Os同位素初始比值187Os/188Os=1.69±0.29,表明石墨来源于富有机质沉积地层。通过测定石墨样品中的有机碳和固定碳,对Re、Os在石墨中的赋存状态进行了研究,表明Re、Os可能是以某种形式赋存在石墨的固定碳中,与其中有机质无关。从原理上解释了石墨的Re-Os同位素年龄反映的是使沉积地层中的炭质变质为石墨,并发生富集迁移的岩浆热变质事件的时期。研究表明石墨的Re-Os同位素分析技术不仅能够为变质作用时间的精确测定提供新的方法,而且对矿床成因的研究也具有重要意义。 相似文献
14.
石灰岩铼-锇同位素分析方法研究及应用初探 总被引：2，自引：2，他引：0
针对石灰岩样品Re-Os同位素分析,在选样和溶样方法上进行了改进,在Carius管封闭前加入HCl与石灰岩反应释放出大量CO2,然后加入氧化剂和稀释剂封闭Carius管溶解样品,大大增加了样品取样量。利用改进的方法对采自青海玉树地区二叠世九十道班组底部的灰黑色微细晶灰岩的Re-Os同位素体系进行了分析测定,得到了精确的沉积年龄(283.1±7.1)Ma(MSWD=0.61,Model1,n=7)。187Os/188Os同位素初始值为0.56±0.12,与二叠纪时海水的187Os/188Os值相一致,反映了石灰岩沉积时海水的187Os/188Os比值。所得石灰岩年龄与其中的生物化石年龄相吻合,并且与区域上岩浆岩锆石年龄相互印证,表明Re-Os同位素体系在该石灰岩中的封闭性较好。通过石灰岩中有机碳含量以及其中Re、Os含量关系研究,得出了Re、Os在灰岩中主要赋存于有机质中的结论。从原理上解释了Re-Os同位素体系在灰岩中的应用具有十分广泛的前景。 相似文献
15.
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
16.
We report the first study of the Re-Os systematics of cobaltite (CoAsS) using disseminated grains and massive sulfides from samples of two breccia-type and two stratabound deposits in the Co-Cu-Au Idaho cobalt belt (ICB), Lemhi subbasin to the Belt-Purcell Basin, Idaho, USA. Using a 185Re + 190Os spike solution, magnetic and non-magnetic fractions of cobaltite mineral separates give reproducible Re-Os analytical data for aliquot sizes of 150 to 200 mg. Cobaltite from the ICB has highly radiogenic 187Os/188Os ratios (17–45) and high 187Re/188Os ratios (600–1800) but low Re and total Os contents (ca. 0.4–4 ppb and 14–64 ppt, respectively). Containing 30 to 74% radiogenic 187Os, cobaltite from the ICB is amenable to Re-Os age determination using the isochron regression approach.Re-Os data for disseminated cobaltite mineralization in a quartz-tourmaline breccia from the Haynes-Stellite deposit yield a Model 1 isochron age of 1349 ± 76 Ma (2σ, n = 4, mean squared weighted deviation MSWD = 2.1, initial 187Os/188Os ratio = 4.7 ± 2.2). This middle Mesoproterozoic age is preserved despite a possible metamorphic overprint or a pulse of metamorphic-hydrothermal remobilization of pre-existing cobaltite that formed along fold cleavages during the ca. 1190–1006 Ma Grenvillian orogeny. This phase of remobilization is tentatively identified by a Model 3 isochron age of 1132 ± 240 Ma (2σ, n = 7, MSWD = 9.3, initial 187Os/188Os ratio of 9.0 ± 2.9) for cobaltite in the quartz-tourmaline breccia from the Idaho zone in the Blackbird mine.All Mesoproterozoic cobaltite mineralization in the district was affected by greenschist- to lower amphibolite-facies (garnet zone) metamorphism during the Late Jurassic to Late Cretaceous Cordilleran orogeny. However, the fine- to coarse-grained massive cobaltite mineralization from the shear zone-hosted Chicago zone, Blackbird mine, is the only studied deposit that has severely disturbed Re-Os systematics with evidence for a linear trend of mixing with (metamorphic?) fluids.The new Re-Os ages and extremely high initial 187Os/188Os ratios of cobaltite reported here favor a magmatic-hydrothermal genetic model for a multi-stage REE-Y-Co-Cu-Au mineralization occurring at ca. 1370 to 1349 Ma, and related to the emplacement of the Big Deer Creek granite pluton at ca. 1377 Ma. In our model, deposition of paragenetically early xenotime and gadolinite was followed by an influx of Mesoproterozoic evaporitic brines and magmatic-hydrothermal fluids containing metals and reduced sulfur derived from mafic and oceanic island-arc Archean to Paleoproterozoic rocks in the Laurentian basement. Cobaltite mineralization occurred upon cooling of these fluids at an inferred temperature of 300 °C or below. 相似文献
17.
含有普通锇的辉钼矿Re-Os同位素定年研究 总被引：14，自引：3，他引：11
通过大量数据统计,表明较高比例的辉钼矿中存在普通锇。普通锇可能以类质同像形式存在于辉钼矿样品中,理论上辉钼矿中可能含有较高含量普通锇。辉钼矿样品含有较高含量普通锇可能对Re-Os定年结果产生很大影响,从原理上并结合实例证实了普通锇含量对辉钼矿Re-Os年龄影响程度。对于一般辉钼矿样品来讲,如果187Os总量(放射成因187Os与非放射成因187Os之和)与普通锇比值小于20,需要考虑普通锇对Re-Os模式年龄的影响,并提出了对于含有普通锇辉钼矿模式年龄的计算方法。先做出187Os/188Os-187Re/188Os等时线,求得初始187Os/188Os值,再根据初始187Os/188Os值和单个样品的普Os含量求得非放射成因的普Os中187Os的量。最后根据Re含量以及放射成因187Os含量得到模式年龄。 相似文献
18.
Using improved analytical techniques, which reduce the Re blanks by factors of 8 to 10, we report new Re-Os data on low Re and low PGE pallasites (PAL-anom) and IIIAB irons. The new pallasite samples nearly double the observed range in Re/Os for pallasites and allow the determination of an isochron of slope 0.0775 ± 0.0008 (T = 4.50 ± 0.04 Ga, using the adjusted λ187Re = 1.66 × 10−11 a−1) and initial (187Os/188Os)0 = 0.09599 ± 0.00046. If the data on different groups of pallasites (including the “anomalous” pallasites) are considered to define a whole-rock isochron, their formation would appear to be distinctly younger than for the iron meteorites by ∼60 Ma. Five IIIAB irons (Acuna, Bella Roca, Chupaderos, Grant, and Bear Creek), with Re contents ranging from 0.9 to 2.8 ppb, show limited Re/Os fractionation and plot within errors on the IIAB iron meteorite isochron of slope 0.07848 ± 0.00018 (T = 4.56 ± 0.01 Ga) and initial (187Os/188Os)0 = 0.09563 ± 0.00011. Many of the meteorites were analyzed also for Pd-Ag and show 107Ag enrichments correlated with Pd/Ag, requiring early formation and fractionation of the FeNi metal, in a narrow time interval, after injection of live 107Pd (t1/2 = 6.5 Ma) into the solar nebula. Based on Pd-Ag, the typical range in relative ages of these meteorites is ≤10 Ma. The Pd-Ag results suggest early formation and preservation of the 107Pd-107Ag systematics, both for IIIAB irons and for pallasites, while the younger Re-Os apparent age for pallasites suggests that the Re-Os system in pallasites was subject to re-equilibration. The low Re and low PGE pallasites show significant Re/Os fractionation (higher Re/Os) as the Re and PGE contents decrease. By contrast, the IIIAB irons show a restricted range in Re/Os, even for samples with extremely low Re and PGE contents. There is a good correlation of Re and Ir contents. The correlation of Re and Os contents for IIIAB irons shows a similar complex pattern as observed for IIAB irons (Morgan et al., 1995), and neither can be ascribed to a continuous fractional crystallization process with uniform solid-metal/liquid-metal distribution coefficients. 相似文献
19.
Robert A Creaser Poulomi Sannigrahi Thomas ChackoDavid Selby 《Geochimica et cosmochimica acta》2002,66(19):3441-3452
Re-Os isotopic analyses of a single organic-rich sedimentary rock unit (ORS) of known depositional age, and at three levels of regional hydrocarbon maturity, show that hydrocarbon maturation does not affect the ability the 187Re-187Os chronometer to yield a depositional age for such rocks. We present Re-Os isotope analyses from the Late Devonian Exshaw Formation in the subsurface of the Western Canada Sedimentary Basin, Alberta, and obtain a Re-Os isochron age of 358 ± 10 Ma (2σ, Model 3, λ = 1.666 × 10−11.a−1) for samples ranging from hydrocarbon immature to overmature. This age is within uncertainty of the established absolute age for the Exshaw Formation. Hydrocarbon immature, and mature plus overmature samples show no significant age differences if regressed individually, indicating that hydrocarbon maturation did not greatly disturb the Re-Os isotope system in the Exshaw Formation. As such, we propose that the Re-Os geochronometer may be used as a reliable tool for measuring the depositional ages of ORS regardless of their level of hydrocarbon maturity. We find that minimizing natural variation in the initial 187Os/188Os ratio is more important than avoiding hydrocarbon maturation in obtaining precise Re-Os ages. In particular, the Exshaw Formation appears to contain a nonhydrogenous component of unradiogenic Os, in addition to the hydrogenous Os load. A subset of Exshaw Formation samples with >5% total organic carbon (TOC), which should best reflect the hydrogenous Os load alone, yields a very well-fitted isochron having a depositional age of 358 ± 9 Ma (2σ, λ = 1.666 × 10−11.a−1) with an initial 187Os/188Os ratio of 0.59 ± 0.05 (Model 3, Mean Square of Weighted Deviates (MSWD) = 1.8). The initial 187Os/188Os ratio of this regression may provide an estimate of the Os isotopic composition of local seawater at the time of deposition. 相似文献
20.
The Yushui Cu-polymetallic deposit, which is associated with Ag, Pb, and Zn, is located in the middle part of the Yongan–Meixian Late Paleozoic Hercynian depression. It was discovered in eastern Guangdong Province in the late 1980s and is one of the richest copper deposits in China with high-grade copper averaging 3.25% and locally reaching 50–60%. The main ore body is located along the unconformity between the Upper Carboniferous Hutian Group limestone and the Lower Carboniferous Zhongxin Formation quartz sandstone with a bedded and lenticular morphology. The ores exhibit massive textures dominated by chalcopyrite, bornite, chalcocite, pyrite, sphalerite, galena, and a trace amount of argentite. Although researchers began studying the Yushui deposit in the early 1990s, the ore genesis remains controversial because of the lack of precise mineralisation age constraints. In this study, direct Re–Os dating of Cu sulphides aided in facilitating a better understanding of the timing of formation of the Yushui deposit. This study is the first attempt to use the Re–Os isotopic system for directly dating chalcopyrite and bornite ores for the Yushui deposit. The contents of Re, common Os, 187Re and 187Os in nine sulphides are 1.68–219.35 ppb, 0.003–0.427 ppb, 1.05–137.31 ppb, and 0.045–0.734 ppb, respectively. The isotope data yielded an isochron age of 308 ± 15 Ma (mean square weighted deviates = 2.4) using the 87Re/188Os–187Os/188Os plot, which is interpreted to represent the age of formation for these sulphides, suggesting that the mineralisation age of the Yushui deposit is close to the age of the host rocks. The 187Os/188Os initial value obtained from the Re–Os isochron is 1.81 ± 0.34, which corresponds to the γOs value of + 1349. This value indicates that the ore-forming materials were derived from the crust without mixing with materials from the mantle, and that the Yushui massive sulphide deposit may be of sedimentary exhalative origin. 相似文献