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首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >Evaluating seawater chemistry from fluid inclusions in halite: Examples from modern marine and nonmarine environments
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Evaluating seawater chemistry from fluid inclusions in halite: Examples from modern marine and nonmarine environments

机译:从盐岩中的流体包裹体评估海水化学性质:现代海洋和非海洋环境中的示例

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Fluid inclusions from marine halites have long been studied to determine the chemical composition of ancient seawater. Chemical analyses of the major ions in fluid inclusions in halites from the solar saltwork of Great Inagua Island, Bahamas, and from the supratidal sabkha, Baja California, Mexico, show that modern marine halites faithfully record the chemical signature of seawater. The major ions in Great Inagua and Baja California fluid inclusions display distinctive linear trends when plotted against one another (ie., Na+, K+, and SO42- vs. Mg2+ and Cl-), which track the evaporation path of seawater as it evolved during the crystallization of halite. These evaporation paths defined for the major ions by fluid inclusions in halite overlap findings of computer simulations of the evaporation of modern seawater by the Harvie, Moller, and Weare (HMW) computer program. The close match between the HMW seawater evaporation paths and the Great Inagua fluid inclusion data is not surprising considering the carefully controlled inflow, evaporation, and discharge of seawater at the Great Inagua saltwork. The major ion chemistry of fluid inclusions from the Baja California halites matches the HMW seawater evaporation paths int most respects, but one Baja fluid inclusion has lower concentrations of Mg2+ than evaporated seawater. Nonmarine inflows and syndepositional recycling of preexisting salts in the Baja California supratidal setting were not large enough to override the chemical signature of evaporating seawater as the primary control on the Baja fluid inclusion compositions. Fluid inclusions in halites from the nonmarine Qaidam Basin, Qinghai Province, western China, have a distinctly different major ion chemical signature than does "global" seawater. The fluid inclusion chemistries from the Qaidam Basin halites do not lie on the evaporation pathways defined by modern seawater and can clearly be differentiated from fluid inclusions containing evaporated seawater. If fluid inclusions in halites from modern natural settings contain unmistakable samples of evaporated seawater, then evaluation of the chemistry of ancient seawater by chemical analysis of fluid inclusions in ancient marine halites by means of the same approach should be valid. Copyright (C) 2001 Elsevier Science Ltd. [References: 40]
机译:长期以来,人们一直在研究海洋卤石中的流体包裹体,以确定古代海水的化学成分。对来自巴哈马大伊纳瓜岛的太阳盐场和墨西哥下加利福尼亚州萨布哈地的盐岩中卤石中流体包裹体中主要离子的化学分析表明,现代海洋卤石忠实地记录了海水的化学特征。相互绘制时,Great Inagua和Baja California流体包裹体中的主要离子表现出独特的线性趋势(即Na +,K +和SO42-与Mg2 +和Cl-),它们追踪海水在蒸发过程中的蒸发路径。盐岩的结晶。这些由盐岩中的流体包裹体为主要离子定义的蒸发路径与Harvie,Moller和Weare(HMW)计算机程序对现代海水蒸发的计算机模拟发现重叠。考虑到大伊那瓜盐场的海水流入,蒸发和排放受到精心控制,HMW海水蒸发路径与大伊那瓜流体包裹体数据之间的紧密匹配不足为奇。巴哈加利福尼亚州卤化物中流体包裹体的主要离子化学性质在大多数方面都与HMW海水蒸发路径相匹配,但是一种巴哈流体包裹体的Mg2 +浓度低于蒸发的海水。在Baja California的潮汐上游环境中,非海洋物质的流入和现有盐的同沉积物再循环不足以覆盖蒸发的海水的化学特征,作为对Baja流体包裹体成分的主要控制。来自中国西部青海省柴达木盆地波罗的海盆地卤化物中的流体包裹体,其主要离子化学特征与“全球”海水截然不同。柴达木盆地卤石的流体包裹体化学物质并不位于现代海水定义的蒸发路径上,并且可以与包含蒸发海水的流体包裹体明显区分开。如果现代自然环境中的卤化物中的流体包裹体包含无误的蒸发海水样品,则采用相同方法通过对古代海洋卤石中的流体包裹体进行化学分析来评估古代海水的化学成分应该是有效的。版权所有(C)2001 Elsevier Science Ltd. [引用:40]

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