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Partitioning behavior of trace elements between dacitic melt and plagioclase, orthopyroxene, and clinopyroxene based on laser ablation ICPMS analysis of silicate melt inclusions

机译:基于激光烧蚀的硅酸盐熔体包裹体的ICpms分析,在英安岩熔体和斜长石,斜方辉石和单斜辉石之间微量元素的分配行为

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摘要

Partitioning behavior of Sc, Ti, V, Mn, Sr, Y, Zr, Nb, Ba, La, Nd, Sm, Eu, Gd, Dy, Ho, Yb, Hf, and Pb between dacitic silicate melt and clinopyroxene, orthopyroxene, and plagioclase has been determined based on laser ablation-inductively coupled plasma mass spectrometric (LA-ICPMS) analysis of melt inclusions and the immediately adjacent host mineral. Samples from the 1988 eruption of White Island, New Zealand were selected because petrographic evidence suggests that all three mineral phases are in equilibrium with each other and with the melt inclusions. All three phenocryst types are found as mineral inclusions within each of the other phases, and mineral inclusions often coexist with melt inclusions in growth-zone assemblages. Compositions of melt inclusions do not vary between the different host minerals, suggesting that boundary layer processes did not affect compositions of melt inclusions and that post-trapping modifications have not occurred. Partition coefficients were calculated from the host and melt inclusion compositions and results were compared to published values. All trace elements examined in this study except Sr are incompatible in plagioclase, and all measured trace elements except for Mn are incompatible in orthopyroxene. In clinopyroxene, Sc, V, and Mn are compatible, and Y, Ti, HREE, and the MREE are only slightly incompatible. Most partition coefficients overlap the wide range of values reported in the literature, but the White Island data are consistently at the lower end of the range in published values. Results from the literature obtained using modern microanalytical techniques such as secondary ion mass spectrometry (SIMS) or proton induced X-ray emission spectroscopy (PIXE) also fall at the lower end of the published values, whereas partition coefficients determined from bulk analysis of glass and crystals separated from volcanic rocks typically extend to higher values. Rapid crystal growth-rates, crystal zonation, or the presence of accessory mineral inclusions in phenocrysts likely accounts for the wide range and generally higher partition coefficients obtained using bulk sampling techniques. The results for 3+ cations from this study are consistent with theoretical predictions based on a lattice strain model for site occupancy. The results also confirm that the melt inclusion-mineral (MIM) technique is a reliable method for determining partition coefficients, as long as the melt inclusions have not experienced post-entrapment reequilibration.
机译:Sc,Ti,V,Mn,Sr,Y,Zr,Nb,Ba,La,Nd,Sm,Eu,Gd,Dy,Ho,Yb,Hf和Pb在硅酸盐硅酸盐熔体与斜辉石,邻位辉石之间的分配行为斜长石是根据熔体包裹体和紧邻的主体矿物的激光烧蚀-电感耦合等离子体质谱(LA-ICPMS)分析确定的。选择1988年新西兰怀特岛火山喷发的样本,是因为岩相学证据表明所有三个矿物相彼此之间以及与熔体包裹体处于平衡状态。在所有其他相中都发现了所有三种隐晶类型为矿物夹杂物,并且矿物夹杂物通常与生长带组合中的熔融夹杂物共存。熔体夹杂物的组成在不同的主体矿物之间没有变化,这表明边界层过程不会影响熔体夹杂物的组成,并且捕集后的改性也没有发生。从主体和熔体夹杂物组成计算分配系数,并将结果与​​公布的值进行比较。在本研究中检查的所有痕量元素(除Sr外)在斜长石中均不相容,而所有测得的痕量元素(除Mn之外)在邻二甲苯中均不相容。在斜茂铁中,Sc,V和Mn是相容的,而Y,Ti,HREE和MREE只是略微不相容。大多数分配系数与文献中报道的宽范围值重叠,但怀特岛的数据始终处于已公布值范围的低端。使用现代微分析技术(如二次离子质谱(SIMS)或质子诱导的X射线发射光谱(PIXE))获得的文献结果也落在已发表值的下端,而分配系数由玻璃和玻璃的体积分析确定从火山岩中分离出来的晶体通常会延伸到更高的值。快速的晶体生长速率,晶体的带状分布,或在隐晶石中存在辅助矿物夹杂物,可能解释了使用大容量采样技术获得的宽范围和更高的分配系数。该研究中3+阳离子的结果与基于位点占据的晶格应变模型的理论预测一致。结果还证实,只要熔体夹杂物没有经历包埋后重新平衡,熔融矿物-矿物(MIM)技术是确定分配系数的可靠方法。

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