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Dispersed Carbon in Basalts of the Altered Oceanic Crust: Isotope Composition and Mechanisms of Formation

机译:蚀变大洋地壳玄武岩中的分散碳:同位素组成和形成机制

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Carboncontents and isotopic compositions were compared in the basalt groundmass of the oceanic crust of different age in the zone of the East Pacific Rise. In samples the basalt groundmass of the ancient oceanic crust (similar to 270 Ma, ODP Site 801C) in which a carbonate phase was found, the isotopic composition of the oxidized carbon (delta C-13 = +/- 1.5 parts per thousand indicates that this carbon was formed by the precipitation of seawater dissolved inorganic carbon (DIC). In the samples in which no carbonate phase was identified, the low concentration (<0.1 wt % CO2) of oxidized dispersed carbon and its isotopic composition (delta C-13 < -7 parts per thousand) are in the range of values typical of carbon dissolved in basalt glasses without crystallinity. This makes it possible to relate the oxidized dispersed carbon to residual carbon dissolved in the magmatic melt after CO2 degassing. The precipitation of DIC results in a positive correlation between the concentration of total carbon and its delta C-13 values, along with the formation of a carbonate phase. The application of this criterion to basalt groundmass samples of the young crust (similar to 15 Ma, ODP Site 1256D) showed that oxidized dispersed carbon in the young oceanic crust groundmass was not formed by the precipitation of DIC, contradicting the generally accepted paradigm. Constant concentration and delta C-13 values of the reduced dispersed carbon in the basalt groundmass of the young and ancient oceanic crusts, including lithological zones where microbial activity has not been recorded, indicate that the most probable model is high-temperature abiogenic generation of reduced dispersed carbon near the ridge axis. The Fischer-Tropsch synthesis and/or Bell-Boudouard reaction provide a possible basis for the abiogenic model. The Bell-Boudouard reaction 2CO = C + CO2 leads to the formation of an adsorbed layer of elemental carbon on the fresh surfaces of minerals during background alteration of the oceanic basalt crust. The CO2-CO gas-phase equilibrium maintains the necessary depletion of the newly formed elemental carbon in the C-13 isotope to delta C-13 < -20 parts per thousand. Abiogenic models for the origin of the isotopically light reduced dispersed carbon in the basalt groundmass do not assume the presence of carbon depleted in the heavy C-13 isotope in the magmatic melt.
机译:比较了东太平洋隆起带不同年龄洋壳玄武岩基质的碳含量和同位素组成。在发现碳酸盐相的古代洋壳玄武岩基质(类似于270 马,ODP站点801C)的样品中,氧化碳的同位素组成(delta C-13 = +/- 1.5千分之一表明该碳是由海水溶解无机碳(DIC)沉淀形成的。在未鉴定碳酸盐相的样品中,氧化分散碳的低浓度(<0.1 wt % CO2)及其同位素组成(δ C-13 <千分之 -7)处于溶解在无结晶度的玄武岩玻璃中的碳的典型值范围内。这使得将氧化分散的碳与CO2脱气后溶解在岩浆熔体中的残余碳联系起来成为可能。DIC的沉淀导致总碳浓度与其δC-13值呈正相关,并形成碳酸盐相。将该标准应用于年轻地壳的玄武岩基质样品(类似于15 马,ODP站点1256D)表明,年轻洋壳基质中的氧化分散碳不是由DIC的沉淀形成的,这与普遍接受的范式相矛盾。年轻和古老大洋结壳玄武岩基质中还原分散碳的恒定浓度和δ C-13值表明,最可能的模型是在山脊轴附近高温非生物生成还原分散碳。费托合成和/或Bell-Boudouard反应为非生物成因模型提供了可能的基础。Bell-Boudouard 反应 2CO = C + CO2 导致在海洋玄武岩地壳的背景蚀变期间在矿物的新鲜表面上形成吸附的元素碳层。CO2-CO气相平衡将C-13同位素中新形成的元素碳维持在δC-13的必要消耗<千分之20。玄武岩基质中同位素轻还原分散碳起源的非生物成因模型不假设岩浆熔体中重C-13同位素中存在耗尽的碳。

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