Petrogenesis of Neoproterozoic high-K calc-alkaline granites forming large batholiths in SE Brazil: Clues from trace-element chemistry of apatite, titanite and hornblende

IF 2.9 2区 地球科学 Q2 GEOCHEMISTRY & GEOPHYSICS
Valdecir de Assis Janasi, Lucelene Martins, Bárbara Bueno Toledo, Adriana Alves, Silvio Roberto Farias Vlach
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引用次数: 0

Abstract

Granites may lose or gain residual melts respectively by compaction and reactive porous flow, and therefore their composition is potentially different from that of the original magmas. Consequently, the chemistry of individual minerals with well-understood textural relationships should be prioritized for inferring magma sources and crystallization conditions. We investigated the major and trace element chemistry of coexisting apatite, titanite and hornblende in thin sections of I-type high-K calc-alkaline (HKCA) granitic rocks forming two voluminous Neoproterozoic batholiths in SE Brazil. Detailed textural studies, major-element analyses by EPMA, and trace-element analyses by LA-ICPMS bring key information on magma genesis and evolution. Titanite is absent or forms thin rims in ferri-ilmenite in granites from Socorro Batholith, resulting from magmatic crystallization at higher temperatures (>800 °C) compared to similar granites from the Agudos Grandes Batholith, where it occurs as large crystals preserving temperature-related zonation, reflected in decreasing LREE and Zr contents. The influence of titanite crystallization is particularly evident in the trace-element chemistry of hornblende and apatite from the Agudos Grandes granites, with one order of magnitude lower REE contents and smaller to suppressed negative Eu anomalies. Systematically higher Sr/Y (and in part also La/Yb) of hornblende, apatite and titanite from Agudos Grandes granites confirms suggestions that they equilibrated at significantly greater depths (and by inference in a thicker crust) as compared to the Socorro granites. Quantitative estimates of Sr/Y in the original melts are hampered by coprecipitation of minerals that accommodate these elements and by potential Sr diffusion, especially in apatite. However, as an early-crystallizing phase in granitic magmas, apatite trace-element composition is a precious source of petrogenetic information; in our study, it reveals that most of the volume of the Agudos Grandes granites crystallized below 800 °C (i.e., after titanite starts to crystallize) and confirms, in agreement with other proxies, that the two batholiths crystallized under oxidizing conditions (e.g., sulfur in apatite up to 800 ppm).
巴西东南部新元古代高钾钙碱性花岗岩形成大岩基的岩石成因:磷灰石、钛矿和角闪石微量元素化学线索
花岗岩可能通过压实作用和反应性多孔流动作用分别失去或获得残余熔体,因此其成分可能与原始岩浆不同。因此,在推断岩浆来源和结晶条件时,应优先考虑具有良好结构关系的单个矿物的化学性质。研究了巴西东南部两大块新元古代高钾钙碱性(HKCA)花岗质岩石中共存的磷灰石、钛矿和角闪石的主微量元素化学特征。详细的结构研究、EPMA主元素分析和LA-ICPMS微量元素分析为岩浆成因和演化提供了重要信息。与Agudos Grandes基的花岗岩相比,Socorro基的铁钛铁矿中没有钛铁矿或形成薄边缘,这是由于岩浆结晶温度(>800°C)高于Agudos Grandes基的花岗岩,在Agudos Grandes基的花岗岩中,钛铁矿以大晶体形式存在,保持了与温度相关的分带,反映在LREE和Zr含量降低。钛矿结晶对阿古多斯花岗岩角闪石和磷灰石微量元素化学的影响尤为明显,稀土元素含量降低一个数量级,且Eu负异常较小至抑制。Agudos Grandes花岗岩中角闪石、磷灰石和钛矿的Sr/Y(部分La/Yb)较高,证实了与Socorro花岗岩相比,它们在更深的深度(推断在更厚的地壳中)达到平衡。原始熔体中Sr/Y的定量估计受到容纳这些元素的矿物的共沉淀和潜在的Sr扩散的阻碍,特别是在磷灰石中。磷灰石微量元素组成作为花岗岩岩浆中的早结晶阶段,是岩石成因信息的宝贵来源;在我们的研究中,它揭示了Agudos Grandes花岗岩的大部分体积在800°C以下结晶(即在钛矿开始结晶之后),并与其他指标一致,证实了两个岩基在氧化条件下结晶(例如,磷灰石中的硫高达800 ppm)。
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来源期刊
Lithos
Lithos 地学-地球化学与地球物理
CiteScore
6.80
自引率
11.40%
发文量
286
审稿时长
3.5 months
期刊介绍: Lithos publishes original research papers on the petrology, geochemistry and petrogenesis of igneous and metamorphic rocks. Papers on mineralogy/mineral physics related to petrology and petrogenetic problems are also welcomed.
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