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1.
富有机物流体中一些重要Ge同位素的平衡分馏参数 总被引：1，自引：1，他引：0
锗（Ge）同位素在地球化学领域有着潜在的应用意义,但是Ge同位素平衡分馏参数的缺乏,严重制约了其在相关研究中的应用。本研究提供了富有机物流体中物种Ge（OH）4、GeO（OH）3^-以及Ge的一些亲有机质络合物（Ge与邻苯二酚、柠檬酸以及草酸配合形成的络合物）之间的Ge同位素平衡分馏参数。用基于Urey模型（或称Bigeleisen-Mayer公式）理论,结合量子化学计算的方法,在B3LYP／6-311＋G（d,p）理论水平下计算了这些Ge同位素平衡分馏系数,其中,溶液效应用精确的“水滴法”来处理。预测这些基本分馏参数的误差约为±0．2‰。纯水溶液中,△Ge（OH）4-GeO（OH）3^-约为0．6‰,海水中稍小,约为0．3‰;而△Ge（OH）4-Ge-邻苯二酚、△Ge（OH）4-Ge-草酸、△Ge（OH）4-Ge-柠檬酸（c）和△Ge（OH）4-Ge柠檬酸（d）非常大,分别约为4．4‰、3．5‰、3．8‰和3．9‰。这些大的分馏或许可以用来示踪生物作用参与过程。结果表明,轻的Ge同位素将富集在富有机质的环境,如煤系、黑色页岩及一些缺氧的条件下,因此这些环境可能存在一个轻Ge同位素的“汇”。 相似文献
2.
采用密度泛函方法模拟了阳离子对水体中B(OH)3和B(OH)4-的影响,计算海水的硼同位素平衡分馏参数。模拟海水环境时,选择基于分子簇模型的"水滴"法,以最多12个水分子环绕兴趣分子的方式构建"水滴"。对海水环境的计算结果显示,B(OH)3和B(OH)4-的硼同位素平衡分馏系数在25?C时为1.031,与纯水环境下的该分馏值并无明显差别。研究表明前人对B(OH)3和B(OH)4-间硼同位素平衡分馏参数的实验测定可能存在问题。研究结果为精进硼同位素古环境重建工作和硼同位素平衡分馏测定提供了理论制约。 相似文献
3.
西藏驱龙斑岩铜矿铜同位素研究 总被引：9，自引：1，他引：8
本文通过Cu的同位素组成示踪斑岩型铜矿床Cu的来源,探讨岩浆-热液过程中Cu同位素的分馏.选择驱龙矿区从早到晚的三期热液脉以及早期钾硅酸盐化蚀变同期的样品,挑选新鲜的黄铜矿,测定其Cu同位素组成.早期A脉:为不规则石英-钾长石脉、石英-硬石膏脉及黑云母脉,δ~(65)Cu的范围为-0.44‰～-0.09‰,集中在-0.44‰～-0.31‰,平均值-0.29‰;B脉,为石英+硬石膏+黄铜矿±辉钼矿±黄铁矿脉和绿帘石-石英脉,δ~(65)Cu的范围为-0.42‰～+0.14‰,集中在-0.25‰～-0.18‰,平均值-0.18‰;晚期D脉,为板状黄铜矿-黄铁矿及黄铁矿脉,δ~(65)Cu的范围为-0.27‰～+0.47‰,集中在-0.27‰～-0.05‰,平均值-0.02‰;早期钾硅酸盐蚀变带,δ~(65)Cu的范围为-0.47‰～-0. 1‰,平均值-0.29‰.矿区铜同位素组成基本同岩浆岩一致(Zhu et al.,2000,2002;Maréchal et al.,1999,2002),表明Cu主要来自斑岩岩浆.不同期次热液的Cu同位素具有明显的分馏,早期相对富集~(63)Cu,晚期相对亏损~(63)Cu,A脉与B脉的同位素组成的差异可能与岩浆-热液演化过程有关,D脉的同位素组成差异可能是大气降水大量混入的结果. 相似文献
4.
《吉林大学学报(地球科学版)》2015,(Z1)
<正>硅元素的丰度在地壳中仅次于氧,是所有硅酸盐矿物的主要成分。然而,有关于地球表层系统(即土壤、水体、植物)的硅同位素分布问题还存在许多不解之处。比如,Georg等(2007)和Hughes等(2013)在室温下由瑞利模型推导的黏土和其溶液的硅同位素平衡分馏系数分别为Δ30Siclay-solution=-1.5‰和-2.05‰,这明显违背化学键越强越富集重同位素的常识。理论上,沉淀的矿物由于其相对于溶液中的H4SiO 4具有较短的Si-O键会优先富集重同位素。类似的现象还存在于石英与溶液的分馏过程。绝大多数现场观测表明, 相似文献
5.
大别造山带天柱山燕山期中酸性岩浆岩元素和同位素地球化学研究 总被引：9，自引：0，他引：9
大别-苏鲁造山带中生代岩浆岩的物质来源和成因机制,是大陆碰撞造山带研究的热点和前沿问题之一。本文通过对大别造山带天柱山燕山期中酸性岩进行全岩主量和微量元素以及放射成因同位素、单矿物氧同位素分析,指示这些碰撞后岩浆岩是俯冲陆壳物质再循环的产物。研究发现,这些中酸性岩表现出明显的轻稀土富集、高场强元素Nb、Ta和Ti负异常以及Pb正异常。它们都具有较高的Sr同位素初始比值(0．7062-0．7083)和较低的εNd(t)值(-17．1--19．7),与北大别杂岩的变化范围一致。单矿物氧同位素变化范围较大(石英:7．48-9．16‰,钾长石:3．76-7．80‰,斜长石:2．06- 6．96‰,锆石:4．16-5．83‰),大多数样品锆石具有与正常地慢锆石(5．3±0．3‰)一致的δ18O值。大多数样品的石英-锆石之间达到并保存了岩浆结晶时的氧同位素平衡分馏,而其它矿物(如钾长石、斜长石、黑云母和角闪石)与锆石之间大多表现为明显的氧同位素不平衡分馏,表明它们受到了岩浆期后亚固相水-岩相互作用的扰动。元素、Sr-Nd同位素和锆石氧同位素特征表明,大别山中生代中性岩可能是由加厚的扬子板块基性下地壳脱水部分熔融并经结晶分异形成的,花岗岩是由化学组成类似于北大别TTG片麻岩的中性下地壳脱水部分熔融形成的。 相似文献
6.
前寒武纪条带状硅铁建造的形成机制与地球早期的大气和海洋 总被引：16，自引：1，他引：15
前寒武纪条带状硅铁建造(BIFs)是地球早期特有的化学沉积建造类型,记录了当时大气和海洋的化学成分、氧化还原状态及演化。本文系统测定了华北地台条带状硅铁建造的硫硅氧同位素组成。不同时代和不同类型条带状硅铁建造中石英的硅同位素组成非常相似,强烈亏损30Si,δ30SiNBS-28大部分位于-2.0‰～-0.3‰之间,平均-0.8‰;硅铁建造中石英的δ18OV-SMOW相对较高,8.1‰～21.5‰,平均13.9‰;二者均与现代海底黑烟囱、泉华及热水沉积硅质岩的硅氧同位素组成相似。在同一样品中,磁铁矿条带中石英的δ30SiNBS-28普遍低于相邻硅质条带中石英的值,而δ18OV-SMOW刚好相反,反映了硅铁建造沉积时的初始特征。BIFs中硫化物的δ34SV-CDT变化范围很大,-22.0‰～+11.8‰,但大部分集中分布在0值附近。Δ33S=-0.89‰～+1.2‰,显示出了明显的硫同位素非质量分馏特征,说明当时大气氧浓度很低。与火山活动关系密切的Algoma型硅铁建造的Δ33S多为负值,而远离火山活动中心的Superior型硅铁建造的Δ33S多为正值。提出无论是Algoma型,还是Superior型BIFs都是由海底热液喷气作用形成的。富含溶解硅和铁的热水溶液喷发到在海底以后,由于温度突然下降,硅酸H4SiO4在海水中达到过饱和状态,导致SiO2首先沉淀,形成硅质层;随着热水溶液与海水的不断混合,温度不断降低,Eh值不断升高,Fe2+逐渐被氧化生成Fe3+随后沉淀,形成富铁层。一套硅铁韵律层代表了一次大的海底喷气活动;海底热液喷气的周期性活动形成了规律性的硅铁韵律层。BIFs的广泛分布和硫同位素非质量分馏效应的普遍存在,表明当时大气氧水平很低,可能不足现在氧水平的1‰;火山和海底喷气活动非常强烈,海水温度较高,呈酸性,pH值在3.0～5.5之间;海洋中可溶解硅H4SiO4和Fe2+的浓度很高;而可溶硫酸盐的浓度极低,1mM。早元古代(1.8Ga)以后海洋硫酸盐浓度升高,由富铁海洋转化为富硫酸盐的海洋,是造成BIFs消失的根本原因。大规模火山喷发和海底喷气活动对海洋的成分和氧化还原状态影响很大,使海洋的氧化时间较大气至少推迟了6亿年。 相似文献
7.
新疆望峰金矿区成矿流体的Si同位素示踪研究及其成矿意义 总被引：1，自引：1，他引：0
新疆望峰金矿区金的成矿作用与硅化作用密切相关,文章通过对矿区典型矿体的赋矿围岩、蚀变岩石及矿石进行Si同位素组成研究,探讨了成矿流体中硅质来源、演化过程及其成矿意义。结果表明:1望峰金矿体围岩具有较均一的Si同位素组成,δ30Si=-0.2‰(n=3),显示了花岗质原岩Si同位素组成特征,动力变质作用对原岩硅同位素组成无明显影响;2蚀变岩石Si同位素组成均一性较高,δ30Si=-0.1‰(n=3),显示了花岗质原岩Si与成矿期热液Si的混合特征;3矿石Si同位素组成变化范围较大,不同类型矿石的Si同位素组成差异较明显:硅化蚀变糜棱岩型δ30Si=-0.5‰~-0.2‰(n=9),集中于-0.3‰~-0.2‰,平均-0.3‰;硅化蚀变岩型δ30Si=-0.3‰~-0.1‰(n=9),平均-0.2‰;热液石英脉型δ30Si=-0.3‰~0.1‰(n=6),平均-0.1‰。望峰金矿区金成矿流体中的硅质,主要来源于花岗质赋矿围岩。矿石中Si同位素组成变化较大,是富硅成矿流体演化过程中发生Si同位素动力学分馏的结果,矿体下部及矿区深部应有一定的找矿前景。 相似文献
8.
本文报道了南岭地区两个花岗岩(大东山和千里山)的全岩以及主要造岩矿物(黑云母、斜长石和石英)的硼含量和硼同位素组成。结果显示,黑云母含有最高的硼含量,斜长石次之,石英中的硼含量则非常低。花岗岩中的硼可能主要以晶格替换方式赋存在黑云母和斜长石中,而石英中的微量硼则来自其包裹的流体包裹体。同时,黑云母具有最低的硼同位素组成,斜长石次之,而石英则具有最高的硼同位素组成。本次研究首次发现花岗岩中的主要造岩矿物间存在着较大的硼同位素分馏:大东山花岗岩中黑云母与斜长石之间存在着-9.3‰的分馏,黑云母与石英之间存在-9.9‰的分馏;千里山花岗岩中黑云母与斜长石之间存在着-6.6‰的分馏,黑云母与石英之间存在着-10.2‰的硼同位素分馏。结合镜下观察和氧同位素研究发现,造成不同矿物间这一大的硼同位素分馏的原因很可能是岩浆后期的热液蚀变作用。综合以往所发表的研究数据,得到含四次配位硼为主的硅酸盐矿物与中酸性热液流体之间的硼同位素分馏方程:1000lnα硅酸盐-流体=-11.19×(103/T[K])+5.09,该分馏是由于硼的四次配位和三次配位之间的转换引起的。 相似文献
9.
为确定元素 B 掺入进珊瑚的形式、B(OH)与 B(OH)3间的分馏系数及珊瑚中微量元素对硼同位素?4组成的影响,对北海涠洲岛、海南三亚和雷州半岛灯楼角三地活体珊瑚的 Mg、Sr、Na、Ca、B 浓度及硼同位素组成(δ11Bcoral)进行了测定.结果表明,涠洲岛、三亚和灯楼角三地珊瑚的 Mg、Sr、Na 和 Ca 浓度平均值分别为40.1 mmol/L、86.1 mmol/L、449 mmol/L 和12.1 mol/L.珊瑚中 B 浓度的变化范围为4.4~8.4 mmol/L,平均值为5.9 mmol/L.Ca、Sr 在珊瑚中明显富集,而 Mg 在珊瑚中贫化.珊瑚 B 浓度的变化主要反映了珊瑚生长时海水 pH 值的变化.δ11Bcoral 的变化范围为22.8‰~27.9‰,平均为25.2‰.除与 B 浓度呈弱正相关关系外,δ11Bcoral 与其他四种元素不相关.应用珊瑚硼同位素组成恢复古海水 pH 值时选择同属种珊瑚和判别是否有 Mg(OH)2的存在是必要的.涠洲岛、灯楼角和三亚三地珊瑚与海水间的硼同位素分馏系数αcoral-sw 分别为0.9839、0.9847和0.9850.计算得到的珊瑚与海水 B(OH)3间的分馏系数αcoral-3的变化范围为0.9772~0.9800,平均值为0.9788.该新的α4-3值是准确的,可以用来反演古海水 pH 值.αcoral-sw 和αcoral-3随pH 值的升高分别呈现出增大和减小的变化趋势.珊瑚的平均δ11Bcoral 位于理论计算的δ11B4和δ11B3曲线之间,而且都低于原始合成海水的δ11B.这些都表明 B 以 B(OH)3和B(OH)两种形式以变化的比例同时掺入进?4珊瑚,并以B(OH)优先掺入为主.计算得到有0.1%~5.5%(平均值为2.2%)的 B(OH)3掺入进珊瑚中.由于?4 B(OH)3同时掺入进生物碳酸盐,δ11Bcarb=δ11B4的假设不能成立,由所测生物碳酸盐δ11Bcarb 值计算的海水 pH值将产生误差,使δ11B-pH 技术变得更为复杂.通过无机碳酸盐沉积或有孔虫或珊瑚的养殖实验(或者野外观测实验)建立用于重建古海水 pH 值的δ11Bcarb-pH 经验方程是今后的一项重要任务. 相似文献
10.
大别山中生代中酸性岩浆岩锆石U-Pb定年、元素和氧同位素地球化学研究 总被引：10，自引：2，他引：10
对大别山中生代主簿源、天柱山和团岭中酸性岩浆岩进行了锆石U-Pb定年、全岩主量和微量元素分析以及全岩和单矿物的氧同位素分析。结果表明,这些富钾的中酸性侵入岩表现出明显的轻稀土富集和高场强元素(Nb、P和Ti)负异常,与围岩片麻岩之间具有类似的微量元素分布特征和初始Sr-Nd-Ph同位素组成。锆石U-Pb年龄指示了早白垩世(121～131Ma)的岩浆结晶年龄。通过CL照相和SHRIMP定年在某些锆石颗粒中发现了老的继承核,年龄分别为742～815Ma和222Ma。这些新元古代和三叠纪核年龄分别与大别-苏鲁造山带超高压变火成岩原岩年龄和超高压变质年龄一致。尽管石英和锆石具有较小的δ~(18)O值变化范围(石英:6.30‰～8.66‰,锆石:4.14‰～6.11‰),全岩和其它单矿物氧同位素比值变化较大(全岩:0.07‰～7.13‰,钾长石:0.55‰～7.40‰,斜长石:-4.88‰～6.96‰),大多数锆石具有与正常地幔锆石(5.3±0.3‰)一致的δ~(18)O值。大多数样品的石英-锆石之间保存了氧同位素平衡分馏,而其它矿物(如,钾长石、斜长石、黑云母和角闪石)与锆石之间则大多表现出明显的氧同位素不平衡分馏,指示它们受到了岩浆期后亚固相水-岩相互作用的扰动。元素和同位素特征表明,大别山中生代中性岩起源于加厚基性下地壳的脱水部分熔融,在岩浆侵位过程中伴随有结晶分异作用;而花岗岩则起源于与北大别TTG正片麻岩具有相似化学组成的中性地壳的部分熔融。因此,大别山中生代中酸性岩岩浆源区是三叠纪扬子陆块俯冲产生的加厚地壳,形成机制可能与早白垩世地幔超柱事件热扰动所引起的部分熔融有关。 相似文献
11.
Rachelle B. Turnier Yaron Katzir Kouki Kitajima Ian J. Orland Michael J. Spicuzza John W. Valley 《Journal of Metamorphic Geology》2020,38(1):53-70
Corundum (Crn), including sapphire, occurs in emery pods surrounded by marble on the island of Naxos, Greece. The emery formed from bauxite deposited in karst that was metamorphosed to 400–700°C at 20–15 Ma. Many of these rocks initially appeared well suited for refractory accessory mineral (RAM) thermometry, which uses oxygen isotope fractionation between a RAM – corundum – and a modally dominant phase with faster diffusion of oxygen – calcite (Cc) – to determine peak metamorphic temperatures. However, previous attempts at oxygen isotope thermometry were confounded by highly variable fractionations (Δ18O) measured at mm-scale and the uncertain calibration of Δ18O(Cc-Crn) versus temperature. Secondary ion mass spectrometry (SIMS) permits in situ analysis of δ18O in corundum and calcite at the 10-μm scale in adjacent grains where textures suggest peak metamorphic equilibrium was attained. SIMS analyses of adjacent mineral pairs in eight rocks yield values of Δ(Cc-Crn) that systematically decrease from 7.2 to 2.9‰ at higher metamorphic grade. Pairing these data with independent temperature estimates from mineral isograds yields an empirical calibration of 1,000 lnα(Cc-Crn) = 2.72 ± 0.3 × 106/T2 (T in K). The new fractionations (2.7‰ at 1,000 K) are significantly smaller than those calculated from the modified increment method (6.5‰ at 1,000 K; Zheng, Geochimica et Cosmochimica Acta, 1991, 55:2299–2307; Zheng, Mineral Mag, 1994, 58A:1000–1001), which yield unreasonably high temperatures of 630 to 1,140°C when applied to the new Naxos data. The new calibration of Δ(Cc-Crn) can be combined with published fractionations to calculate A-factors for corundum versus a range of 14 other minerals. These new fractionation factors can be used for thermometry or to constrain the genesis of corundum. A compilation of gem corundum δ18O values shows that many igneous sapphires, including important deposits of basalt-associated sapphire, are mildly elevated in δ18O relative to the calculated range in equilibrium with mantle values (4.4–5.7‰) and formed from evolved magmas. 相似文献
12.
河南栾川地区是我国著名斑岩钼矿集区,近年铅锌矿勘查取得重要进展,但对铅锌矿成因认识分歧颇多。研究表明,栾川地区铅锌矿产在燕山期斑岩钼矿床外围,矿区地层为中元古界官道口群和新元古界栾川群碳酸盐岩-碎屑岩沉积变质建造,地层中侵入有晋宁期辉长岩、正长岩和燕山期酸性斑岩,铅锌矿呈脉状或透镜状,发育3种类型:受燕山期斑岩与元古界钙质地层接触带控制的夕卡岩型铅锌矿、受北西西向层间断裂构造控制的脉状铅锌矿和受北东或近南北向张-张扭性断裂控制的脉状铅锌矿。铅锌矿石中硫化物δ~(34)S_(V-CDT)为近零的正值(骆驼山0.37‰～4.20‰、赤土店-0.32‰～8.30‰、百炉沟-1.20‰～10.90‰、冷水北沟0.70‰～12.10‰),岩浆来源硫特征明显;夕卡岩型铅锌硫化物的δ~(34)S_(V-CDT)与本地斑岩型钼矿石中硫化物的δ~(34)S_(V-CDT)(1.24‰～3.30‰)极为相近,脉状铅锌硫化物的δ~(34)S_(V-CDT)与斑岩型钼矿石中硫化物重合,但有地层中硫(δ~(34)S_(V-CDT)为12.43‰～18.63‰)的影响。总体上δ~(34)S_(黄铁矿)>δ~(34)S_(闪锌矿)>δ~(34)S_(方铅矿),指示矿石中主要硫化物矿物硫同位素分馏基本达到平衡,赤土店铅锌矿石中共生方铅矿与闪锌矿的硫同位素温度计指示硫化物矿物沉淀温度较高(388.29℃)。河南栾川地区铅锌矿主体应为受燕山期构造-岩浆作用控制的中高温热液铅锌矿床。 相似文献
13.
《地学前缘(英文版)》2022,13(5):101250
Sulfur mass-independent fractionation (S-MIF) preserved in Archean sedimentary pyrite is interpreted to reflect atmospheric chemistry. Small ranges in Δ33S that expanded into larger fractionations leading up to the Great Oxygenation Event (GOE; 2.45–2.2 Ga) are disproportionately represented by sequences from the Kaapvaal and Pilbara Cratons. These patterns of S-MIF attenuation and enhancement may differ from the timing and magnitude of minor sulfur isotope fractionations reported from other cratons, thus obscuring local for global sulfur cycling dynamics. By expanding the Δ33S record to include the relatively underrepresented São Francisco Craton in Brazil, we suggest that marine biogeochemistry affected S-MIF preservation prior to the GOE. In an early Neoarchean sequence (2763–2730 Ma) from the Rio das Velhas Greenstone Belt, we propose that low δ13Corg (<?30‰) and dampened Δ33S (0.4‰ to ?0.7‰) in banded iron formation reflect the marine diagenetic process of anaerobic methane oxidation. The overlying black shale (TOC up to 7.8%) with higher δ13Corg (?33.4‰ to ?19.2‰) and expanded Δ33S (2.3‰ ± 0.8‰), recorded oxidative sulfur cycling that resulted in enhance preservation of S-MIF input from atmospheric sources of elemental sulfur. The sequence culminates in a metasandstone, where concomitant changes to more uniform δ13Corg (?30‰ to ?25‰), potentially associated with the RuBisCO I enzyme, and near-zero Δ33S (?0.04‰ to 0.38‰) is mainly interpreted as evidence for local oxygen production. When placed in the context of other sequences worldwide, the Rio das Velhas helps differentiate the influences of global atmospheric chemistry and local marine diagenesis in Archean biogeochemical processes. Our data suggest that prokaryotic sulfur, iron, and methane cycles might have an underestimated role in pre-GOE sulfur minor isotope records. 相似文献
14.
Oxygen isotope compositions and magmatic epidote from two contrasting metaluminous granitoids,NE Brazil 总被引：1，自引：0，他引：1
Oxygen isotope compositions of mineral separates were determined from two metaluminous granitoids (Emas and São Rafael plutons) from northeastern Brazil. The I-type Emas pluton has high δ18O (WR) values (11.5–11.8‰), whereas the São Rafael pluton has low δ18O (WR) values (7.5–8.1‰), but Sr and Nd are characteristics of S-type granitoids. Measured mineral–mineral fractionations suggest continuous sub-solidus inter-mineral isotope exchange among all minerals except zircon. There is a large and consistent quartz–epidote fractionation that gives apparent temperatures that are much lower than anticipated closure temperatures for epidote. Oxygen isotope fractionation between natural zircon and magmatic epidote is opposite to that predicted from theoretical determinations, as δ18O (epidote) <δ18O (zircon). An empirical calibration based on these results would suggests a closure T for oxygen in epidote of ~500 °C and Δ(qtz–epi) ~5.19 at 500 °C. 相似文献
15.
Raphaelle Escoube Olivier J. Rouxel Béatrice Luais Emmanuel Ponzevera Olivier F.X. Donard 《Geostandards and Geoanalytical Research》2012,36(2):149-159
Recent analytical developments in germanium stable isotope determination by multicollector ICP‐MS have provided new perspectives for the use of Ge isotopes as geochemical tracers. Here, we report the germanium isotope composition of the NIST SRM 3120a elemental reference solution that has been calibrated relative to internal isotopic standard solutions used in the previous studies. We also intercalibrate several geological reference materials as well as geological and meteoritic samples using different techniques, including online hydride generation and a spray chamber for sample introduction to MC‐ICP‐MS, and different approaches for mass bias corrections such as sample–calibrator bracketing, external mass bias correction using Ga isotopes and double‐spike normalisation. All methods yielded relatively similar precisions at around 0.1‰ (2s) for δ74/70Ge values. Using igneous and mantle‐derived rocks, the bulk silicate Earth (BSE) δ74/70Ge value was re‐evaluated to be 0.59 ± 0.18‰ (2s) relative to NIST SRM 3120a. Several sulfide samples were also analysed and yielded very negative values, down to ?4.3‰, consistent with recent theoretical study of Ge isotope fractionation. The strong heavy isotope depletion in ore deposits also contrasts with the generally positive Ge isotope values found in many modern and ancient marine sediments. 相似文献
16.
17.
R. ZHAO R. Y. ZHANG J. G. LIOU A. L. BOOTH E. C. POPE C. P. CHAMBERLAIN 《Journal of Metamorphic Geology》2007,25(2):207-224
Two Rongcheng eclogite‐bearing peridotite bodies (Chijiadian and Macaokuang) occur as lenses within the country rock gneiss of the northern Sulu terrane. The Chijiadian ultramafic body consists of garnet lherzolite, whereas the Macaokuang body is mainly meta‐dunite. Both ultramafics are characterized by high MgO contents, low fertile element concentrations and total REE contents, which suggests that they were derived from depleted, residual mantle. High FeO contents, an LREE‐enriched pattern and trace‐element contents indicate that the bulk‐rock compositions of these ultramafic rocks were modified by metasomatism. Oxygen‐isotope compositions of analysed garnet, olivine, clinopyroxene and orthopyroxene from these two ultramafic bodies are between +5.2‰ and +6.2‰ (δ18O), in the range of typical mantle values (+5.1 to +6.6‰). The eclogite enclosed within the Chijiadian lherzolite shows an LREE‐enriched pattern and was formed by melts derived from variable degrees (0.005–0.05) of partial melting of peridotite. It has higher δ18O values (+7.6‰ for garnet and +7.7‰ for omphacite) than those of lherzolite. Small O‐isotope fractionations (ΔCpx‐Ol: 0.4‰, ΔCpx‐Grt: 0.1‰, ΔGrt‐Ol: 0.3–0.4‰) in both eclogite and ultramafic rocks suggest isotopic equilibrium at high temperature. The P–T estimates suggest that these rocks experienced subduction‐zone ultrahigh‐pressure (UHP) metamorphism at ～700–800 °C, 5 GPa, with a low geothermal gradient. Zircon from the Macaokuang eclogite contains inclusions of garnet and diopside. The 225 ± 2 Ma U/Pb age obtained from these zircon may date either the prograde conditions just before peak metamorphism or the UHP metamorphic event, and therefore constrains the timing of subduction‐related UHP metamorphism for the Rongcheng mafic–ultramafic bodies. 相似文献
18.
S. R. DUNN 《Journal of Metamorphic Geology》2005,23(9):813-827
This study presents calcite–graphite carbon isotope fractionations for 32 samples from marble in the northern Elzevir terrane of the Central Metasedimentary Belt, Grenville Province, southern Ontario, Canada. These results are compared with temperatures calculated by calcite–dolomite thermometry (15 samples), garnet–biotite thermometry (four samples) and garnet–hornblende thermometry (three samples). Δcal‐gr values vary regularly across the area from >6.5‰ in the south to 4.0‰ in the north, which corresponds to temperatures of 525 °C in the south to 650 °C in the north. Previous empirical calibration of the calcite–graphite thermometer agrees very well with calcite–dolomite, garnet–biotite and garnet–hornblende thermometry, whereas, theoretical calibrations compare less well with the independent thermometry. Isograds in marble based on the reactions rutile + calcite + quartz =titanite and tremolite + calcite + quartz = diopside, span temperatures of 525–600 °C and are consistent with calculated temperature–X(CO2) relations. Results of this study compare favourably with large‐scale regional isotherms, however, local variation is greater than that revealed by large‐scale sampling strategies. It remains unclear whether the temperature–Δcal‐gr relationship observed in natural materials below 650 °C represents equilibrium fractionations or not, but the regularity and consistency apparent in this study demonstrate its utility for thermometry in amphibolite facies marble. 相似文献
19.
浙江江山寒武系碳酸盐岩碳氧同位素特征及其古环境意义探讨 总被引：8，自引：1，他引：8
对浙江江山碓边下寒武统上部—下奥陶统下部碳酸盐岩进行了碳氧同位素测定。δ1 3C、δ1 8O值变化范围和均值分别为 - 1.9‰～ 3.7‰、- 13.0‰～ - 1.3‰和 0 .86‰、- 9.76‰。碳氧同位素地层曲线与 Veizer et al.(1986 )的同位素年代演化曲线形状相似 ,在寒武纪—奥陶纪界线附近没有明显的δ1 3C、δ1 8O漂移现象。δ1 3C地层曲线具旋回性变化特征 ,大陈岭组、杨柳岗组各形成一个完整的演化旋回 ,与根据露头层序地层研究推测的海平面变化曲线吻合性较好 ,表现出δ1 3C值的高值区是海盆水体变深的反映。一个明显的碳同位素正漂移发生于晚寒武世早期 (华严寺组下部 ) ,与 Matthew etal.(2 0 0 0 )报道的在美国内华达州中东部、哈萨克斯坦 Malyi Karatau地区、澳大利亚昆士兰州西北部和湘西桃源瓦儿岗等地发现的 δ1 3C正漂移记录 (SPICE— The Steptoean Positive CarbonIsotope Excursion)和 Veizer et al.(1986 )碳同位素年代演化曲线中的正漂移波峰一致 ,为晚寒武世全球性碳同位素正漂移提供了一个佐证。 相似文献