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首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >Correction for volatile fractionation in ascending magmas: Noble gas abundances in primary mantle melts
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Correction for volatile fractionation in ascending magmas: Noble gas abundances in primary mantle melts

机译:校正上升岩浆中的挥发分馏:原始地幔熔体中的稀有气体丰度

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Accurate relative noble gas abundances of mantle-derived melts are required in order to further understand the distribution of noble gases in the mantle and fractionation of noble gases during the melting process. Noble gas relative abundances in the majority of oceanic basalts are highly fractionated, at least in part due to late stage, solubility controlled fractionation. Noble gas concentrations in the volatile phase (≡ noble gas:CO_2 ratio) will vary systematically during solubility controlled degassing of a magma. This contribution models the noble gas concentrations in the volatile phase during degassing at different pressures and vesicularities in order to develop a method for correcting fractionation resulting from magmatic degassing, and thereby estimate the "initial" (pre-degassing) noble gas compositions. Correcting for fractionation during magmatic degassing requires: a) a method for determining the volatile fractionation trajectory during degassing; and b) one well constrained mantle volatile composition with which to "fix" the extrapolation. The trajectory of volatile fractionation can be estimated by sequential crushing of basaltic glasses. Vesicles grow during ascent, therefore large vesicles trap early (less fractionated) volatiles while small vesicles trap late (fractionated) volatiles. Sequential crushing of basaltic glasses releases volatiles from progressively smaller vesicles, thereby allowing the fractionation trajectory resulting from degassing to be determined on individual samples. The production rate of both ~(21)Ne and ~4He in the mantle is a function of U concentration only, resulting in a constant ~(21)Ne/~4He production ratio in the mantle which can be used to "fix" the degassing fractionation trajectory determined by sequential crushing. This correction then allows fractionation of ~4He from ~(40)Ar prior to degassing to be assessed. This method is illustrated using multiple crushes of a single basaltic glass from the mid-Atlantic Ridge that shows that ~4He appears to have been fractionated from ~(40)Ar before degassing.
机译:为了进一步了解稀有气体在地幔中的分布以及稀有气体在熔融过程中的分馏,需要精确地相对于稀有的地幔来源的稀有气体丰度。大多数海洋玄武岩中的稀有气体相对丰度高度分馏,至少部分是由于后期的溶解度控制分馏所致。在溶解度控制的岩浆脱气过程中,挥发性相中的稀有气体浓度(稀有气体:CO_2比)将系统地变化。该贡献对在不同压力和囊泡下的脱气过程中的挥发性相中的稀有气体浓度进行建模,以便开发一种校正因岩浆脱气而产生的分馏的方法,从而估算“初始”(预脱气)稀有气体的成分。在岩浆脱气过程中进行分馏校正需要:a)确定脱气过程中挥发性分馏轨迹的方法; b)一种约束良好的地幔挥发性成分,用以“固定”外推。可以通过依次压碎玄武玻璃来估算挥发分馏的轨迹。囊泡在上升过程中生长,因此大囊泡捕获较早(分级分离的)挥发物,而小囊泡捕获较晚(分级分离的)挥发物。依序粉碎玄武玻璃可从逐渐变小的囊泡中释放出挥发物,从而可以对单个样品确定由脱气产生的分馏轨迹。地幔中〜(21)Ne和〜4He的产生率仅是U浓度的函数,导致地幔中恒定的〜(21)Ne /〜4He产生率,可用于“固定”通过顺序破碎确定脱气分馏轨迹。然后,该校正可以评估脱气前从〜(40)Ar中〜4He的分馏。大西洋中脊单个玄武质玻璃的多次压碎说明了该方法,结果表明〜4He似乎是在脱气之前从〜(40)Ar中分离出来的。

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