Elizabeth A. Bell , Heather M. Kirkpatrick , T. Mark Harrison
{"title":"Promises and pitfalls of source terrane prediction from inclusions in detrital zircon","authors":"Elizabeth A. Bell , Heather M. Kirkpatrick , T. Mark Harrison","doi":"10.1016/j.chemgeo.2025.122899","DOIUrl":null,"url":null,"abstract":"<div><div>Understanding the relationship between the assemblage of mineral inclusions trapped by an igneous zircon suite and the composition of the host magma is complicated by processes that preclude simple relationships between, for example, the relative proportions of modal mineral inclusions (e.g., quartz, alkali feldspar, and plagioclase; QAP) and the degree of magma differentiation. However, apatite and ferromagnesian inclusion abundances can be approximately related to the SiO<sub>2</sub> content in some magmas, potentially allowing for broad inferences of source rock composition from detrital zircon mineral inclusion suites. This study presents mineral inclusion assemblages in igneous zircon from a wide range of magma compositions, tectono-magmatic settings, and geographic locations to better determine the correlation between major inclusion phases and source rock chemistry. We find that the relationship between apatite and whole rock SiO<sub>2</sub> is strongly dependent on the aluminosity (as shown by A/CNK) of the source rock, with peraluminous and metaluminous rocks showing opposite trends. For inclusion assemblages containing less than about 30–40 % apatite, discrimination of highly silicic peraluminous from mafic-intermediate metaluminous granitoid sources is possible. Metaluminous samples display a broad increase in whole rock phosphate content with increasing apatite inclusion abundance, potentially allowing estimation of lower limits on protolith phosphate abundance. The ratio of ferromagnesian to late-crystallizing inclusions exceeds 0.5 mostly for mafic-intermediate samples, with some exceptions. Inclusion phases concentrating highly incompatible trace elements exceed 5 % of the inclusion suite only in highly silicic (>70 % SiO<sub>2</sub>) granites. However, there is no discernable relationship between QAP and whole rock chemistry, with inclusion QAP from compositionally diverse magmas clustering in a similar region of the QAP diagram. Application of these observations to several first-generation sediments derived from granitoid terranes suggests that apatite abundance, the ratio of ferromagnesian to late-crystallizing silicate inclusions, and trace elements can help select between peraluminous vs. metaluminous sources and help to distinguish mafic-intermediate from highly silicic source rocks. This could have wide applicability to using the detrital zircon record to infer petrogenetic provenance.</div></div>","PeriodicalId":9847,"journal":{"name":"Chemical Geology","volume":"690 ","pages":"Article 122899"},"PeriodicalIF":3.6000,"publicationDate":"2025-05-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Geology","FirstCategoryId":"89","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S000925412500289X","RegionNum":2,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GEOCHEMISTRY & GEOPHYSICS","Score":null,"Total":0}
引用次数: 0
Abstract
Understanding the relationship between the assemblage of mineral inclusions trapped by an igneous zircon suite and the composition of the host magma is complicated by processes that preclude simple relationships between, for example, the relative proportions of modal mineral inclusions (e.g., quartz, alkali feldspar, and plagioclase; QAP) and the degree of magma differentiation. However, apatite and ferromagnesian inclusion abundances can be approximately related to the SiO2 content in some magmas, potentially allowing for broad inferences of source rock composition from detrital zircon mineral inclusion suites. This study presents mineral inclusion assemblages in igneous zircon from a wide range of magma compositions, tectono-magmatic settings, and geographic locations to better determine the correlation between major inclusion phases and source rock chemistry. We find that the relationship between apatite and whole rock SiO2 is strongly dependent on the aluminosity (as shown by A/CNK) of the source rock, with peraluminous and metaluminous rocks showing opposite trends. For inclusion assemblages containing less than about 30–40 % apatite, discrimination of highly silicic peraluminous from mafic-intermediate metaluminous granitoid sources is possible. Metaluminous samples display a broad increase in whole rock phosphate content with increasing apatite inclusion abundance, potentially allowing estimation of lower limits on protolith phosphate abundance. The ratio of ferromagnesian to late-crystallizing inclusions exceeds 0.5 mostly for mafic-intermediate samples, with some exceptions. Inclusion phases concentrating highly incompatible trace elements exceed 5 % of the inclusion suite only in highly silicic (>70 % SiO2) granites. However, there is no discernable relationship between QAP and whole rock chemistry, with inclusion QAP from compositionally diverse magmas clustering in a similar region of the QAP diagram. Application of these observations to several first-generation sediments derived from granitoid terranes suggests that apatite abundance, the ratio of ferromagnesian to late-crystallizing silicate inclusions, and trace elements can help select between peraluminous vs. metaluminous sources and help to distinguish mafic-intermediate from highly silicic source rocks. This could have wide applicability to using the detrital zircon record to infer petrogenetic provenance.
期刊介绍:
Chemical Geology is an international journal that publishes original research papers on isotopic and elemental geochemistry, geochronology and cosmochemistry.
The Journal focuses on chemical processes in igneous, metamorphic, and sedimentary petrology, low- and high-temperature aqueous solutions, biogeochemistry, the environment and cosmochemistry.
Papers that are field, experimentally, or computationally based are appropriate if they are of broad international interest. The Journal generally does not publish papers that are primarily of regional or local interest, or which are primarily focused on remediation and applied geochemistry.
The Journal also welcomes innovative papers dealing with significant analytical advances that are of wide interest in the community and extend significantly beyond the scope of what would be included in the methods section of a standard research paper.