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首页> 外文期刊>Minerals >Formation of Authigenic Low-Magnesium Calcite from Sites SS296 and GC53 of the Gulf of Mexico
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Formation of Authigenic Low-Magnesium Calcite from Sites SS296 and GC53 of the Gulf of Mexico

机译:从墨西哥湾的SS296和GC53矿床形成自成因的低镁方解石

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Authigenic low-magnesium calcite (LMC)—a mineral phase that should precipitate in calcite seas rather than today’s aragonite sea—was recently discovered at the seafloor of the Gulf of Mexico (GoM) at water depths of 65 m (site SS296) and 189 m (site GC53). This study investigates the mineralogical, petrographic, and geochemical characteristics of LMC from both sites to reveal its formation process. The δ 18 O values of LMC from site SS296 cluster in two groups (?0.6‰ to 1.7‰; 6.3‰ to 7.5‰) and the presence of cone-in-cone texture in the samples with lower δ 18 O values suggest precipitation at higher temperatures and greater depth. Low δ 18 O values of LMC from site GC53 ranging from ?9.4‰ to ?2.5‰ indicate an influence of meteoric waters during formation. LMC at both sites reveals a wide range of δ 13 C values (?17.4‰ to 2.6‰), indicating various carbon sources including seawater and/or organic matter. This interpretation is further supported by the δ 13 C values of organic carbon extracted from the LMC lithologies (δ 13 C org : from ?26.8‰ to ?18.9‰). Relatively low Sr concentrations of LMC samples regardless of variable 87 Sr/ 86 Sr ratios, ranging from 0.707900 to 0.708498 for site GC53 and from 0.709537 to 0.710537 for site SS396, suggest the exchange of Sr between pore fluids and ambient sediments/rocks. The observed wide range of 87 Sr/ 86 Sr ratios and the enrichment of Fe and Mn in LMC is in accordance with pore fluids deriving from the dissolution of Louann salt. Overall, this study reveals that the formation of LMC at sites SS296 and GC53 was favored by the presence of low Mg/Ca ratio pore fluids resulting from salt dissolution in subsurface environments when sufficient dissolved inorganic carbon was available. These results are essential for understanding the formation of marine LMC at times of an aragonite sea, highlighting the role of formation environments—open environments close to or at the seafloor vs. confined subseafloor environments typified by pore waters with a composition largely different from that of seawater.
机译:自发性低镁方解石(LMC)是一种应在方解石海而不是今天的文石海中沉淀的矿物相,最近在墨西哥湾(GoM)的海底处发现了水深65 m(SS296位置)和189 m(网站GC53)。这项研究调查了这两个地点的LMC的矿物学,岩石学和地球化学特征,以揭示其形成过程。来自SS296簇的LMC的δ18 O值分为两组(?0.6‰到1.7‰; 6.3‰到7.5‰),并且在较低δ18 O值的样品中存在锥形锥结构,表明在更高的温度和更大的深度。来自GC53站点的LMC的低δ18 O值在9.4‰到2.5‰之间,这表明在形成过程中流域水的影响。两个地点的LMC都显示出很宽的δ13 C值范围(?17.4‰至2.6‰),表明包括海水和/或有机物在内的各种碳源。从LMC岩性中提取的有机碳的δ13 C值(δ13 C org:从?26.8‰至?18.9‰)进一步支持了这种解释。 LMC样品的Sr浓度相对较低,无论其可变的87 Sr / 86 Sr比率如何(对于GC53站点为0.707900至0.708498,对于SS396站点为0.709537至0.710537),表明孔隙流体与周围沉积物/岩石之间的Sr交换。观察到的广泛的87 Sr / 86 Sr比范围以及LMC中Fe和Mn的富集与卢安盐溶解产生的孔隙流体有关。总的来说,这项研究表明,当有足够的溶解的无机碳存在时,由于盐在地下环境中的溶解而导致的低Mg / Ca比孔隙流体的存在,有利于在SS296和GC53位形成LMC。这些结果对于了解文石海时期海洋LMC的形成至关重要,突出了形成环境的作用-靠近或位于海底的开放环境与以孔隙水为代表的密闭海底环境(其组成与海水的组成大不相同)海水。

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