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1.
蓬莱金矿区位于胶东三大金矿带中的栖霞-蓬莱金矿带内。本文系统研究了该金矿化集中区内的黑岚沟、大柳行和河西金矿的 S、Pb、Rb-Sr 同位素地球化学特征,并与招远-掖县成矿带中的玲珑金矿化集中区内的大型-超大型金矿床进行了对比研究。蓬莱金矿区δ~(34)S 值总体变化为6.3‰～9.5‰,平均值为7.5‰。其中河西金矿δ~(34)S 值为7.4‰～8.5‰,黑岚沟金矿δ~(34)S 值为6.3‰～9.5‰,大柳行金矿δ~(34)S 值为6.4‰～8.2‰。不同矿床的硫同位素组成差异十分小,并与玲珑金矿区的硫同位素组成相近(δ~(34)S=6.4‰～8.6‰,平均值为7.6‰)。蓬莱金矿区的铅同位素组成变化小,其中河西金矿~(206)Pb/~(204)Pb 为17.3086～17.4799,~(207)Pb/~(204)Pb 为15.5264～15.5543,~(208)pb/~(204)Pb 为38.0642～38.3698;大柳行金矿~(206)Pb/~(204)Pb 为17.3653～ 17.5037.~(207)Pb/~(204)Pb 为15.5142～15.5355,~(208)Pb/~(204)Pb 为38.1249～38.31 36:黑岚沟金矿~(206)Pb/~(204)Pb 为17.3558～17.5958,~(207)Ph/~(204)Pb 为15.5105～15.5746,~(208)Pb/~(204)Pb为38.0749～38.4361。投影到 Zartman and Doe(1981)铅构造模式图上,成分点落在造山带演化线附近。蓬莱金矿区与玲珑金矿区的铅同位素组成基本一致,部分数据与矿区内煌斑岩的铅同位素组成相近,而与赋矿围岩郭家岭花岗岩相差甚远,表明矿体中的铅可能与煌癍岩有相同的源区。矿石铅呈线性趋势分布,它正好位于煌斑岩与一个极具放射成因铅的胶东群地层的铅同位素组成之间,很可能说明矿石铅是壳幔混合的产物。对蓬莱金矿区黄铁矿的 Rb-Sr 同位素分析结果表明,河西金矿的成矿年龄为122.3±3.1Ma(MSWD=1.7),初始~(87)Sr/~(86)Sr 比值为0.71208;黑岚沟和大柳行金矿的成矿年龄为117.8±6.5Ma(MSWD=17),初始~(87)Sr/~(86)Sr 比值为0.71085。说明蓬莱金矿区具有与玲珑金矿区相近的成矿时代,两者均为120Ma 左右。锶同位素初始比值也说明成矿物质具有壳慢混合的特征。从蓬莱金矿区具有与玲珑金矿区一致的地质、地球化学和年代学特征可知,蓬莱金矿区具有产出大型一超大型金矿的巨大远景。  相似文献   

2.
驱龙铜矿是西藏陆陆碰撞造山带冈底斯斑岩铜矿带内代表性矿床之一。本文对其含矿斑岩和矿石矿物进行了S、Pb同位素组成分析。驱龙矿床含矿斑岩与矿石矿物的硫同位素组成比较一致,含矿斑岩δ34S为-2.1‰~-1.1‰,黄铜矿δ34S为-6.3‰~-1.0‰,均值-2.76‰;硬石膏δ34S为 12.5‰~ 14.4‰,平均 13.4‰。成矿热液中的硫同位素基本达到了平衡,显示出岩浆硫组成特点。含矿斑岩的206Pb/204Pb范围为18.5104~18.6083,207Pb/204Pb变化于15.5946~15.7329之间,208Pb/204Pb为38.6821~39.1531之间;矿石矿物黄铜矿的206Pb/204Pb、207Pb/204Pb、208Pb/204Pb分别为18.4426~18.5909、15.5762~15.6145、38.5569~38.8568。含矿斑岩与矿石矿物的铅同位素组成比较一致,它们的变化幅度较小,应具有相同的起源与演化历史。无论是岩石铅还是矿石铅,在铅构造模式图上均位于造山带铅演化曲线上。驱龙矿床硫、铅同位素数据暗示,成矿物质主要来自深源岩浆,含矿斑岩起源于西藏造山带加厚的下地壳熔融,具有幔源成分的混染。  相似文献   

3.
为探讨研究区大规模成矿流体演化特征,对紫云山岩体及其周边的W-Cu、Mo-Cu、Mo、U多金属矿床的硫、铅同位素特征进行了系统研究。研究区的多金属矿硫化物的δ34SCDT为1.2‰~21.1‰,分属1.0‰~3.0‰和21.1‰两个区间附近,分别对应W-Cu-Mo矿化和U矿化,推测研究区的W-Cu-Mo成矿流体中硫以幔源为主,而铀成矿流体则可能是有围岩硫的加入。研究区的W-Cu-Mo多金属矿床的硫化物矿石铅同位素组成:^(208)Pb/^(204)Pb=38.541~38.742,平均38.705;^(207)Pb/^(204)Pb=15.617~15.710,平均15.654;^(206)Pb/^(204)Pb=18.240~18.433,平均18.299。黑钨矿的铅同位素组成:^(208)Pb/^(204)Pb=38.649~39.595,平均39.122;^(207)Pb/^(204)Pb=15.542~15.828,平均15.685;^(206)Pb/^(204)Pb=20.842~21.319,平均21.081。石英的铅同位素组成:^(208)Pb/^(204)Pb=37.683;^(207)Pb/^(204)Pb=15.602;^(206)Pb/^(204)Pb=20.442。紫云山花岗岩铅同位素组成:^(208)Pb/^(204)Pb=38.583~39.182,平均38.943;^(207)Pb/^(204)Pb=15.635~15.683,平均15.657;^(206)Pb/^(204)Pb=18.714~19.276,平均18.937。综合全方位对比法、三参数法和模式图解法,认为研究区成矿物质具有岩浆和地层混合铅的特征,也有部分幔源铅的加入。研究矿区发生的过大规模的双源成矿流体作用以及流体的多阶段演化,导致W-Cu-Mo-U成矿元素共生分异的现象。  相似文献   

4.
凡口铅锌矿床同位素地球化学证据   总被引：3，自引：0，他引：3  
汪礼明  徐文忻  李蘅  彭省临 《地球学报》2005,26(Z1):164-167
对凡口铅锌矿床不同成矿阶段进行矿物包裹体温度、硫和铅同位素测定，获得成矿第Ⅰ阶段温度为300±50℃，第Ⅱ、Ⅲ阶段温度为250±50℃；并获得矿床硫化物的S同位素组成为2.1‰～26.5‰，具有δ34SPy＞δ34SSp＞δ34SGn；第Ⅰ阶段硫化物的硫同位素组成随赋存层位由老到新硫同位素有逐渐减小趋势；第Ⅱ阶段硫化物的δ34S为14.3‰～23.8‰；第Ⅲ阶段硫化物的δ34S为5.7％~15.7‰，具有从早阶段至晚阶段硫同位素组成变化范围从大至小的减小趋势。分析获得68件铅同位素数据，其中硫化物的206Pb/204Pb比值为18.023～18.847；207Pb/204Pb比值为15.700～15.820；208Pb/204Pb比值为38.056～39.796。灰岩全岩的206Pb/204Pb比值为18.230～18.860；207Pb/204Pb比值为15.640～16.000；208Pb/204Pb比值为38.714～39.960。辉绿岩的206Pb/204Pb比值为18.570～18.650；207Pb/204Pb比值为15.260～15.620；208Pb/204Pb比值为38.650～38.960。第Ⅰ阶段δ34OH2O为13.3‰~13.1‰，δD为－50.2‰～－61.5‰；第Ⅱ阶段δ18OH2O为－2.4‰～＋10.8‰，δD为－50.2‰～－63.2‰；第Ⅲ阶段δ18OH2O为－4.9‰～－14.3‰，δD为－59.0‰～－61.0‰。  相似文献   

5.
雪鸡坪斑岩铜矿位于西南三江构造火成岩带义敦岛弧带,其成矿斑岩为印支期石英闪长玢岩和石英二长斑岩。研究对该矿区安山岩、矿化斑岩和矿石矿物系统进行S,Pb同位素分析结果表明:金属硫化物的δ34S值为-3.1‰～ 0.7‰,平均值为-1.1‰,与矿化斑岩的硫同位素组成(-1.4‰和-1.5‰)一致,均落入幔源硫范围,表明硫主要来自岩浆;δ34S黄铁矿(-1.8‰～ 0.7‰,平均-0.5‰)>δ34S黄铜矿(-2.2‰～0.0‰,平均-1.2‰)>δ34S方铅矿(-3.1‰～-1.3‰,平均-2.4‰),硫同位素分馏基本达到平衡。矿石矿物(208Pb/204Pb=37.917～38.230,平均值38.075;207Pb/204Pb=15.528～15.614,平均值15.571;206Pb/204Pb=17.929～18.082,平均值17.981)与矿化斑岩(208Pb/204Pb=37.832、37.883,207Pb/204Pb=15.529、15.538,206Pb/204Pb=17.906、17.910)以及安山岩(208Pb/204Pb=37.816～37.884,207Pb/204Pb=15.549～15.562,206Pb/204Pb=17.845～17.919)的初始铅组成基本一致,变化范围较小,表明三者具有相同的来源;在铅构造模式图上,所有样品铅同位素均位于造山带演化线上或附近,在铅同位素源区判别图中,均落入造山带和下地壳区域,这表明Pb主要来源于壳幔混合。雪鸡坪铜矿S,Pb同位素组成共同指示成矿物质主要来自于深部岩浆,这种岩浆可能主要起源于俯冲洋壳板片的部分熔融并受到少量地壳物质的混染。  相似文献   

6.
大西洋洋中脊TAG热液区硫化物铅和硫同位素研究   总被引：18，自引：3，他引：18  
位于大西洋洋中脊26.08°N的 TAG 热液区是目前己知的赋存在无沉积物覆盖的洋中脊区的一个最大的海底热液硫化物矿床。新测得来自 ODP-158航次钻孔的9件热液硫化物的铅、硫同位素组成;2件铁锰氧化物和1件底盘玄武岩的铅同位素组成。结果表明,矿石硫化物的铅同位素组成~(206)Pb/~(204)Pb 为18.2343～18.3181,~(207)pb/~(204)Ph 为15.4717～15.5061,~(208)Pb/~(204)Pb 为37.7371～37.8417;它们位于该区底盘玄武岩(~(206)Pb/~(204)Pb=18.1454,~(207)Pb/~(204)Pb=15.4572,~(208)Pb/~(204)Pb=37.6534)和近洋底铁锰氧化物(~(206)Pb/~(204)Pb,~(207)Pb/~(204)Pb,~(208)Pb/~(204)Pb 分别为18.6907～18.9264,15.5615～15.6279,38.1164～38.3687)的铅同位素组成之间。三者呈线性相关关系,说明硫化物中铅来源于地幔(玄武岩)与海水(铁锰氧化物)的两端元混合。硫化物的硫同位素组成δ~(34)S 为6.2‰～9.5‰,它明显高于地幔玄武岩的硫同位素组成(δ~(34)S=±0‰),也高于东太平洋海隆 EPR21°N(δ~(34)S=0.9‰～4.0‰)和大西洋洋中脊 MAR23°N(δ~(34)S=1.2‰～2.8‰)等热液活动区硫化物的硫同位素组成,这一特征反映了 TAG 热液体系中硫来源于地幔玄武岩硫与海水硫酸盐无机还原作用产生的硫的两端元混合。此,铅硫同位素研究为现代大洋底热液硫化物矿床形成过程中矿质来源及流体混合作用提供了十分有益的信息。  相似文献   

7.
铜山岭铜多金属矿床是湘南W、Sn、Pb、Zn、Cu多金属矿集区的代表性矿床,本文对其不同类型岩石和矿石矿物进行了S、Pb、C同位素组成对比研究。矿石硫化物的δ34 S值变化范围为-1.9‰~5.7‰,平均值为2.6‰,硫主要来源于硫同位素组成均一化的岩浆。硫化物硫同位素平衡温度表明,矿床主要成矿温度为134~339℃。矿石铅的206 Pb/204 Pb、207 Pb/204 Pb、208 Pb/204 Pb比值分别为18.256~18.856、15.726~15.877、38.352~39.430;岩体岩石铅的206Pb/204Pb、207Pb/204Pb、208Pb/204Pb比值分别为18.617~18.805、15.721~15.786、38.923~39.073;两者铅同位素组成相同,都主要为上地壳铅,是由同一岩浆体系分异形成,可能来源于古老基底岩石。不同类型岩石、方解石矿物的δ13 CPDB值为-9.88‰~1.32‰,δ18 OSMOW值为11.67‰~17.68‰,从矽卡岩矿体到距岩体稍远的围岩地层,方解石矿物的δ13 CPDB、δ18 OSMOW值逐渐增大,成矿流体中的碳早期可能主要来源于岩浆,在成矿过程中有部分碳酸盐岩地层碳的加入。铜山岭矿床成矿物质主要来源于岩浆,赋矿地层对矿床成矿物质来源作用不显著,仅提供了少量成矿物质。  相似文献   

8.
贵州独山巴年锑矿床是华南锑矿带代表性锑矿床之一。矿体赋存于中泥盆统独山组地层之中。本文对该矿床辉锑矿的硫、铅同位素组成进行了系统分析。结果表明,辉锑矿的δ34S值变化范围为-5.4‰～-1.2‰,平均-4.2‰,计算获得成矿流体中总硫的δ34SΣS=0.1‰,显示岩浆来源硫的同位素特征。辉锑矿铅同位素组成变化范围较窄:206Pb/204Pb为18.561～19.156,平均18.813;207Pb/204Pb为15.703～15.769,平均15.734;208Pb/204Pb为38.573～39.207,平均38.906。绝大多数样品中矿石铅为正常铅,具有华南区域性铅同位素组成特征。我们认为巴年锑矿床成矿金属元素锑除主要来源于赋矿围岩泥盆系外,基底地层也可能提供了部分成矿物质。  相似文献   

9.
新城金矿是胶东金矿集区招远—莱州成矿带的一个"焦家式"蚀变型金矿床。本文主要通过C、H、O、S、Pb同位素研究,对新城金矿成矿流体、物质来源和成矿作用进行探讨和研究。新城金矿矿石中δD值范围为-116‰~-91‰,δ18O水值范围为3.8‰~7.2‰,表明成矿流体早期来源于岩浆水,成矿晚期混入大气降水。矿石硫化物、郭家岭花岗闪长岩、玲珑花岗岩和胶东群δ34S平均值分为7.9‰、6.5‰、8.5‰和6.2‰,认为矿石硫具有对矿区地层及岩浆岩硫的继承性。硫化物矿石206Pb/204Pb=17.115~17.414,207Pb/204Pb=15.460~15.577,208Pb/204Pb=37.912~38.196,显示铅具有壳幔混合来源的特征。碳、氢、氧、硫、铅同位素反映新城金矿成矿物质和流体主要来源于深部岩浆。  相似文献   

10.
为了明确内蒙古别鲁乌图铜多金属矿床的成矿年龄与矿床成因,对该矿床中与成矿关系密切的流纹岩进行了锆石U-Pb年龄以及主要金属硫化物的S、Pb同位素测试。其中流纹岩的锆石206Pb/238U加权平均年龄为(271.7±1.6)Ma(MSWD=1.02),显示成矿作用发生于二叠纪。金属硫化物的S同位素分析结果显示δ34SV-CDT值分布在-0.6‰~1.0‰之间,平均为0.49‰,变化范围较窄,显示S的来源单一;Pb同位素组成比较集中,206Pb/204Pb为18.207~18.674,207Pb/204Pb为15.620~15.699,208Pb/204Pb为38.144~38.790,具有壳幔混源的特征。S、Pb同位素特征均指示成矿物质主要来源于岩浆热液。结合区域地质、矿床地质、空间分带等特征以及S、Pb同位素组成可知,别鲁乌图铜多金属矿床为VHMS型矿床,形成于二叠纪陆缘弧裂谷中。  相似文献   

11.
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12.
Radiogenic isotopes in fluid inclusions   总被引：7，自引：0，他引：7  
Igor M. Villa   《Lithos》2001,55(1-4):115-124
Radiogenic isotopes studied in fluid inclusions are still a limited field, with great potential for expansion as analytical techniques improve. The main limitation for Sr, Ar and He isotope work is the very small number of radiogenic atoms produced in a typical fluid inclusion. The requirements to analysts are correspondingly high. Examples show that isotopic tracing on fluid inclusion fluids can be a decisive tool in solving geological problems.  相似文献   

13.
Neoproterozoic chemostratigraphy   总被引：3，自引：0，他引：3  
Chemostratigraphy has diverse applications to investigating the rock record, such as reconstructing paleoenvironments, determining the tectonic setting of sedimentary basins, indirect dating, and establishing regional or global correlations. Chemostratigraphy is thus an integral component of many investigations of the ancient sedimentary record. In this contribution, we review the principle inorganic geochemical methods that have been applied to the Neoproterozoic sedimentary record. Analysis of the traditional stable and radiogenic isotope systems, such as δ13C, δ18O, δ34S, and 87Sr/86Sr, is routine, particularly in successions rich in carbonate. These mainstay applications have yielded invaluable data and information bearing on the chronology and evolution of this eventful era in Earth history. Alongside the growing database of traditional data, a series of novel geochemical techniques have given rise to important new models and constraints on Neoproterozoic biogeochemical change. In particular, a range of proxies for water column redox, mainly obtained from black shales, have shed light on the pace and tempo of Neoproterozoic oxygenation and its link to the appearance of early animal evolution. Increased integration of diverse geochemical, sedimentological, and paleontological datasets, and the gradual radiometric calibration of the stratigraphic record promise to bring the details of the evolution of the Neoproterozoic Earth system into ever greater focus.  相似文献   

14.
硫、氧同位素和放射性同位素比值在示踪岩浆与围岩的反应及在岩浆镍-铜-铂族元素矿床成因中同化过程的重要性方面有很大作用。如1.1Ga的Duluth杂岩、Norilsk地区二叠-三叠纪侵入岩和1.4Ga的Kabanga侵入岩体中矿床的硫同位素测定结果证明硫来自含硫化物和硫酸盐的围岩。1.3Ga的VoisbeysBay矿床矿石的硫同位素δ34S值通常落入公认的地幔硫同位素组成范围(0±2‰)内,而对其元古宙变质沉积围岩进行的详细研究结果显示δ34S的平均值也在此范围。全面了解同位素组成的潜在混染对合理评价提供硫来源的围岩在矿石形成中的作用是非常必要的。用氧同位素和放射性同位素示踪岩浆和围岩相互作用时,必须在开放体系没有扰动同位素系统情况下进行。在氧同位素体系和放射性同位素体系(如Re/Os、Pb同位素体系)中,元素在热液条件下活动性强或主相没有发生同位素交换与吸收,都会导致低温热液过程掩盖高温过程。只有在进行详细的岩相观察和单矿物分析之后,再应用围岩混染同位素模式才是有意义的。  相似文献   

15.
In an effort to constrain the mechanism of dolomitization in Neogene dolomites in the Bahamas and improve understanding of the use of chemostratigraphic tracers in shallow‐water carbonate sediments the δ34S, Δ47, δ13C, δ18O, δ44/40Ca and δ26Mg values and Sr concentrations have been measured in dolomitized intervals from the Clino core, drilled on the margin of Great Bahama Bank and two other cores (Unda and San Salvador) in the Bahamas. The Unda and San Salvador cores have massively dolomitized intervals that have carbonate associated sulphate δ34S values similar to those found in contemporaneous seawater and δ44/40Ca, δ26Mg values, Sr contents and Δ47 temperatures (25 to 30°C) indicating relatively shallow dolomitization in a fluid‐buffered system. In contrast, dolomitized intervals in the Clino core have elevated values of carbonate associated sulphate δ34S values indicating dolomitization in a more sediment‐buffered diagenetic system where bacterial sulphate reduction enriches the residual in 34S, consistent with high sediment Sr concentrations and low δ44/40Ca and high δ26Mg values. Only dolomites associated with hardgrounds in the Clino core have carbonate associated δ34S values similar to seawater, indicating continuous flushing of the upper layers of the sediment by seawater during sedimentary hiatuses. This interpretation is supported by changes to more positive δ44/40Ca values at hardground surfaces. All dolomites, whether they formed in an open fluid‐buffered or closed sediment‐buffered diagenetic system have similar δ26Mg values suggesting that the HMC transformed to dolomite. The clumped isotope derived temperatures in the dolomitized intervals in Clino yield temperatures that are higher than normal, possibly indicating a kinetic isotope effect on dolomite Δ47 values associated with carbonate formation through bacterial sulphate reduction. The findings of this study highlight the utility of applying multiple geochemical proxies to disentangle the diagenetic history of shallow‐water carbonate sediments and caution against simple interpretations of stratigraphic variability in these geochemical proxies as indicating changes in the global geochemical cycling of these elements in seawater.  相似文献   

16.
Pelagic deposits at Abadeh represent a complete biostratigraphic record across the Permian/Triassic boundary (PTB). The presumed water depth during deposition of these sediments was between 60 and 90 m. Similar to other Permian/Triassic boundary sections, the succession at Abadeh is characterised by a negative carbon isotope shift of approximately 4. The values start to decrease in the lower C. changxingensis - C. deflecta s.l. Zone, reach –0.12 (V-PDB) in the uppermost Permian just below the PTB, remain low to the early I. isarcica Zone (–0.32) and increase subsequently in the upper I. isarcica Zone. For the time interval of the PTB negative carbon isotope excursion, between the C. iranica and the I. isarcica Zones, no correlation exists between the 13Ccarb and the 18Ocarb. The above observations argue against the conclusion of Heydari et al. (2001) that the carbon isotope event at the P/T transition is an alteration artefact and not a global signal. The decrease in 13Ccarb is accompanied by a ~5 (and potentially up to 10) increase in 34SSSS. Together, these features are thought to reflect a complex global event, notably the development of widespread anoxic oceans with anoxic bottom layers rising onto the shelves. For the carbon isotope drop, other factors, such as the collapse of ocean primary productivity may also have played a role. The 87Sr/86Sr ratios of Dzhulfian seawater show only a minor increase from 0.70705 to 0.70710, reaching 0.70720 in the Dorashamian. The increase becomes steeper in the Early Triassic reaching 0.70754 in the N. dieneri Zone. The rise of the strontium isotope values is thought to be related to enhanced continental weathering under humid climatic conditions in the uppermost Permian (C. meishanensis - H. praeparvus Zone) and the lack of a dense land vegetation in the Early Triassic, prior to the Spathian (Upper Olenekian).  相似文献   

17.
Mineralogical, textural and geochemical investigations were made to determine the post-depositional evolution of Devonian and Early Carboniferous carbonates from Valle de Tena. The carbonate association is made up of low-Mg calcite, which occurs as micrite, spar cements, neomorphic patches and spar filling veinlets. Non-stoichiometric dolomite and ankerite occur as cements (dolomite also as replacements) in the Middle Devonian, post-dating calcite types. All these phases pre-date tectonic stylolites, indicating compaction after stabilization of the carbonate minerals. Strontium concentrations indicate that Early Devonian and Early Carboniferous micrites initially precipitated as aragonite; Middle and Late Devonian micrites precipitated as high-Mg calcites. Both precursors were diagenetically stabilized to low-Mg calcites through interaction with meteoric waters in phreatic environments. Trace elements in dolomite and ankerite indicate precipitation from Sr-enriched meteoric water. All studied carbonates, except Middle Devonian limestones, precipitated in reducing environments, which favoured incorporation of Fe and Mn. Late calcite generations precipitated from more saline waters than micrites. Light 18O values in micrites suggest alteration mainly in meteoric-phreatic environments. The dolomites and ankerites precipitated from more 18O-depleted fluids than the calcites, suggesting a greater contribution from meteoric waters. Variations in 13C of micrites represent primary secular trends, according to published 13C variations. The 13C oscillations within each succession probably relate to sea-level oscillations. Strontium isotopes also point to a meteoric origin of diagenetic fluids. Model calculations suggest that O and Sr isotopes equilibrated between calcites and fluid at relatively low water/rock ratios, whereas C isotopic signatures are inherited from limestones.  相似文献   

18.
Lithological, chemical, and stable isotope data are used to characterize lacustrine tufas dating back to pre-late Miocene and later unknown times, capping different surfaces of a Tertiary carbonate (Sinn el-Kedab) plateau in Dungul region in the currently hyperarid south-western Egypt. These deposits are composed mostly of calcium carbonate, some magnesium carbonate and clastic particles plus minor amounts of organic matter. They have a wide range of (Mg/Ca)molar ratios, from 0.03 to 0.3. The bulk-tufa carbonate has characteristic isotope compositions: (δ13Cmean = −2.49 ± 0.99‰; δ18Omean = −9.43 ± 1.40‰). The δ13C values are consistent with a small input from C4 vegetation or thinner soils in the recharge area of the tufa-depositing systems. The δ18O values are typical of fresh water carbonates. Covariation between δ13C and δ18O values probably is a reflection of climatic conditions such as aridity. The tufas studied are isotopically similar to the underlying diagenetic marine chalks, marls and limestones (δ13Cmean = −2.06 ± 0.84‰; δ18Omean = −10.06 ± 1.39‰). The similarity has been attributed to common meteoric water signatures. This raises large uncertainties in using tufas (Mg/Ca)molar, δ13C and δ18O records as proxies of paleoclimatic change and suggests that intrinsic compositional differences in material sources within the plateau may mask climatic changes in the records.  相似文献   

19.
Iron is one of the most abundant transition metal in higher plants and variations in its isotopic compositions can be used to trace its utilization. In order to better understand the effect of plant-induced isotopic fractionation on the global Fe cycling, we have estimated by quantum chemical calculations the magnitude of the isotopic fractionation between different Fe species relevant to the transport and storage of Fe in higher plants: Fe(II)-citrate, Fe(III)-citrate, Fe(II)-nicotianamine, and Fe(III)-phytosiderophore. The ab initio calculations show firstly, that Fe(II)-nicotianamine is ～3‰ (56Fe/54Fe) isotopically lighter than Fe(III)-phytosiderophore; secondly, even in the absence of redox changes of Fe, change in the speciation alone can create up to ～1.5‰ isotopic fractionation. For example, Fe(III)-phytosiderophore is up to 1.5‰ heavier than Fe(III)-citrate2 and Fe(II)-nicotianamine is up to 1‰ heavier than Fe(II)-citrate. In addition, in order to better understand the Fe isotopic fractionation between different plant components, we have analyzed the iron isotopic composition of different organs (roots, seeds, germinated seeds, leaves and stems) from six species of higher plants: the dicot lentil (Lens culinaris), and the graminaceous monocots Virginia wild rye (Elymus virginicus), Johnsongrass (Sorghum halepense), Kentucky bluegrass (Poa pratensis), river oat (Uniola latifolia), and Indian goosegrass (Eleusine indica). The calculations may explain that the roots of strategy-II plants (Fe(III)-phytosiderophore) are isotopically heavier (by about 1‰ for the δ56Fe) than the upper parts of the plants (Fe transported as Fe(III)-citrate in the xylem or Fe(II)-nicotianamine in the phloem). In addition, we suggest that the isotopic variations observed between younger and older leaves could be explained by mixing of Fe received from the xylem and the phloem.  相似文献   

20.
镁同位素地球化学研究新进展及其应用   总被引：7，自引：3，他引：4  
作为一种新兴的地质示踪剂,Mg同位素正受到国际地学界日益广泛的关注。Mg同位素地球化学研究已取得了巨大的进展,近期研究工作主要包括两个方面。首先,调查了地球各主要储库和陨石的Mg同位素组成特征,结果表明陨石和地球地幔具有均一并且相似的Mg同位素组成,平均δ26Mg值分别为-0.28±0.06‰和-0.25±0.07‰;相反,上地壳和水圈的Mg同位素组成很不均一,δ26Mg值变化范围分别为-4.84‰~+0.92‰和-2.93‰~+1.13‰。其次,对一些地质和物理化学过程中Mg同位素的分馏行为进行研究,结果表明:(1)地表风化作用可以造成大的Mg同位素分馏,导致重Mg同位素残留在风化产物中而轻Mg同位素进入水圈;(2)岩浆分异过程中Mg同位素平衡分馏很小;(3)高温化学扩散和热扩散过程中Mg同位素会发生显著的动力学分馏。基于这些研究成果,Mg同位素体系已经被初步应用于示踪早期地球形成和壳内物质再循环等过程,并有望在不久的将来应用于示踪大陆地壳的化学演化和地质温度计等研究领域。  相似文献   

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