玄武岩阿连德斜长石-橄榄石包裹体SA-1的形成和结晶的化学和同位素限制

A. Kennedy, I. Hutcheon
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引用次数: 24

摘要

- SA-1是阿连德地区一种罕见的玄武岩斜长石-橄榄石包裹体(POI),具有同心圆的结构和矿物学带,外边界细粒,100μm,内部粗粒,具有亚蛇纹结构。SA-1外边界和内部的辉石、透辉石和橄榄石具有均匀的本质分异,同位素重Mg (FMg = 3.6±1.8‰/amu)。而靠近细晶边界的富尖晶石区尖晶石的Mg同位素组成正常(FMg = 0.1±1.5‰/amu)。大钙(an90,99)斜长石岩心中没有多余的26Mg,对应26Mg*/ 27Al < 3.7 × 10−6。SA-1中Mg同位素的非均质性要求靠近细晶边界的富尖晶石区域的初始冷却速率大于~ 75°C/hr。相反,内部的亚嗜酸性结构表明冷却速度为5-20°C/ hr。SA-1中的矿物表现出广泛的REE丰度。镧的浓度从早晶透辉石中的1 ×球粒石(ch)到晚晶辉石中的100 × ch不等。霞石的LREE含量为18 ~ 20 × ch, HREE含量为11 ~ 25 × ch,富铁介态的REE含量为270 ~ 400 × ch, HREE含量为230 ~ 280 × ch。斜辉石和斜长石的稀土元素互补模式以及不相容微量元素在中晶和结晶后期的富集与封闭体系结晶相一致。霞石的稀土元素和富铁中间体数据表明,这些相处于平衡状态,霞石是熔融结晶。碱、少量铁和卤素的流入一定是在结晶的最后阶段发生的,或者包裹体在钠流入期间一定是部分熔融的,因为包裹体中既有钙长石(An99),也有霞石。熔体结晶的包裹体中同位素不均匀性的保存意味着熔体不完全,允许残余尖晶石存活。SA-1的主微量元素丰度与星云物质混合物的形成不一致,表明SA-1含有由火成岩分异产生的化学分馏成分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chemical and isotopic constraints on the formation and crystallization of SA-1, a basaltic Allende plagioclase-olivine inclusion
— SA-1, an unusual basaltic plagioclase-olivine inclusion (POI) in Allende, has concentric textural and mineralogic zones, a fine-grained, 100μm outer border and a coarse-grained interior with subophitic texture. Fassaite, diopside and olivine from the exterior border and interior of SA-1 have uniform intrinsic mass fractionation with isotopically heavy Mg (FMg = 3.6 ± 1.8‰/amu). In contrast, spinels from the spinel-rich regions adjacent to the fine-grained border have normal Mg isotopic composition (FMg = 0.1 ± 1.5‰/amu). The cores of large calcic (An90,99) plagioclase have no excess 26Mg, corresponding to 26Mg*/ 27Al < 3.7 × 10−6. The Mg isotopic heterogeneity in SA-1 requires initial cooling rates of spinel-rich regions adjacent to the fine-grained border to be greater than ∼75 °C/hr. In contrast, the subophitic texture of the interior suggests cooling rates of 5–20 °C/ hr. The minerals in SA-1 exhibit a wide range of REE abundances. Lanthanum concentrations vary from 1 × chondritic (ch) in early crystallizing diopside to 100 × ch in late crystallizing fassaite. Nepheline has 18–20 × ch LREE and 11–25 × ch HREE and iron-rich mesostasis is highly enriched in the REE with 270–400 × ch LREE and 230–280 × ch HREE. The complementary REE patterns of clinopyroxene and plagioclase and the enrichment of incompatible trace elements in the mesostasis and late crystallizing phases is consistent with closed system crystallization. The REE data for nepheline and the iron-rich mesostasis indicate these phases are in equilibrium and that nepheline crystallized from a melt. Influx of alkalies, minor Fe and halogens must have occurred during the last stages of crystallization or the inclusion must have been partially molten during Na influx as both anorthite (An99) and nepheline are present in this inclusion. The preservation of isotopic heterogeneity in an inclusion that crystallized from a melt implies that melting was incomplete, allowing for survival of the relict spinels. The major and trace element abundances in SA-1 are inconsistent with formation as a mixture of nebular materials and suggest that SA-1 contains a chemically fractionated component produced by igneous differentiation.
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