Xuyang Meng, David R. Mole, A. Simon, Jingwen Mao, D. Kontak, P. Jugo, Jackie Kleinsasser
{"title":"加拿大阿比提比绿岩带>2.7 Ga的异常富硫化物岩浆磷灰石晶体","authors":"Xuyang Meng, David R. Mole, A. Simon, Jingwen Mao, D. Kontak, P. Jugo, Jackie Kleinsasser","doi":"10.2138/am-2024-9387","DOIUrl":null,"url":null,"abstract":"\n Sodic volcanoplutonic terranes in the Archean can be well preserved, but why oxidized S-rich sodic magmas and porphyry-type Cu-Au deposits are so rare remains poorly understood. Here we addressed this issue by measuring the S concentration and S6+/ΣS ratio of primary apatite grains in >2.7 Ga felsic volcanic rocks from the well-characterized Neoarchean Abitibi Greenstone Belt of the Superior Province, Canada. Whereas apatite grains in most samples contain low S concentrations (<0.01 wt%, n = 24), a few apatite samples are S-rich (0.14 ± 0.03 wt%, 1σ) and have low S6+/ΣS ratios (0.56 ± 0.17; 1σ, n = 4). Samples with S-poor apatite have variable whole-rock La/Yb ratios (generally <30) and zircon 10000*(Eu/Eu*)/Yb ratios of 11 ± 8 (1σ), which may be products of plume-driven or over-thickened crustal melting. In contrast, the samples with S-rich apatite have elevated La/Yb ratios of 49 ± 15 (1σ), zircon 10000*(Eu/EuN*)/Yb ratios of 26 ± 7 (1σ), and zircon δ18O values of 5.8 ± 0.1 ‰ (1σ), consistent with a deep, hydrous and homogeneous mantle-like source for the melts dominated by amphibole ± garnet fractionation that is reminiscent of subduction-like process. These are the first reported results documenting the predominant accommodation of relatively reduced S in S-rich apatite grains crystallized from terrestrial silicate melts, possibly reflecting slight oxidation associated with the hydration of Neoarchean mantle and crystal fractionation over the magma evolution. The more common S-poor apatite data suggest that suppressed oxidation of the parental sodic magmas led to weak S emission from Earth’s interior to its evolving surface, explaining the rarity of porphyry-type Cu deposits in > 2.7 Ga Archean sodic volcanoplutonic terranes.","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":" 367","pages":""},"PeriodicalIF":4.7000,"publicationDate":"2024-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Unusual sulfide-rich magmatic apatite crystals from >2.7 Ga Abitibi Greenstone Belt, Canada\",\"authors\":\"Xuyang Meng, David R. Mole, A. Simon, Jingwen Mao, D. Kontak, P. Jugo, Jackie Kleinsasser\",\"doi\":\"10.2138/am-2024-9387\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n Sodic volcanoplutonic terranes in the Archean can be well preserved, but why oxidized S-rich sodic magmas and porphyry-type Cu-Au deposits are so rare remains poorly understood. Here we addressed this issue by measuring the S concentration and S6+/ΣS ratio of primary apatite grains in >2.7 Ga felsic volcanic rocks from the well-characterized Neoarchean Abitibi Greenstone Belt of the Superior Province, Canada. Whereas apatite grains in most samples contain low S concentrations (<0.01 wt%, n = 24), a few apatite samples are S-rich (0.14 ± 0.03 wt%, 1σ) and have low S6+/ΣS ratios (0.56 ± 0.17; 1σ, n = 4). Samples with S-poor apatite have variable whole-rock La/Yb ratios (generally <30) and zircon 10000*(Eu/Eu*)/Yb ratios of 11 ± 8 (1σ), which may be products of plume-driven or over-thickened crustal melting. In contrast, the samples with S-rich apatite have elevated La/Yb ratios of 49 ± 15 (1σ), zircon 10000*(Eu/EuN*)/Yb ratios of 26 ± 7 (1σ), and zircon δ18O values of 5.8 ± 0.1 ‰ (1σ), consistent with a deep, hydrous and homogeneous mantle-like source for the melts dominated by amphibole ± garnet fractionation that is reminiscent of subduction-like process. These are the first reported results documenting the predominant accommodation of relatively reduced S in S-rich apatite grains crystallized from terrestrial silicate melts, possibly reflecting slight oxidation associated with the hydration of Neoarchean mantle and crystal fractionation over the magma evolution. The more common S-poor apatite data suggest that suppressed oxidation of the parental sodic magmas led to weak S emission from Earth’s interior to its evolving surface, explaining the rarity of porphyry-type Cu deposits in > 2.7 Ga Archean sodic volcanoplutonic terranes.\",\"PeriodicalId\":2,\"journal\":{\"name\":\"ACS Applied Bio Materials\",\"volume\":\" 367\",\"pages\":\"\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2024-07-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Bio Materials\",\"FirstCategoryId\":\"89\",\"ListUrlMain\":\"https://doi.org/10.2138/am-2024-9387\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"89","ListUrlMain":"https://doi.org/10.2138/am-2024-9387","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0
摘要
阿寒带的钠质火山岩地层保存完好,但富含S的氧化钠质岩浆和斑岩型铜金矿床为何如此罕见,至今仍不甚明了。在这里,我们通过测量加拿大苏必利尔省特征良好的新奥陶纪阿比提比绿岩带中大于2.7 Ga的长英质火山岩中原生磷灰石晶粒的S浓度和S6+/ΣS比率来解决这个问题。而大多数样本中的磷灰石颗粒都含有较低的 S 浓度(2.7 Ga Archean sodic volcanoplutonic terranes.
Unusual sulfide-rich magmatic apatite crystals from >2.7 Ga Abitibi Greenstone Belt, Canada
Sodic volcanoplutonic terranes in the Archean can be well preserved, but why oxidized S-rich sodic magmas and porphyry-type Cu-Au deposits are so rare remains poorly understood. Here we addressed this issue by measuring the S concentration and S6+/ΣS ratio of primary apatite grains in >2.7 Ga felsic volcanic rocks from the well-characterized Neoarchean Abitibi Greenstone Belt of the Superior Province, Canada. Whereas apatite grains in most samples contain low S concentrations (<0.01 wt%, n = 24), a few apatite samples are S-rich (0.14 ± 0.03 wt%, 1σ) and have low S6+/ΣS ratios (0.56 ± 0.17; 1σ, n = 4). Samples with S-poor apatite have variable whole-rock La/Yb ratios (generally <30) and zircon 10000*(Eu/Eu*)/Yb ratios of 11 ± 8 (1σ), which may be products of plume-driven or over-thickened crustal melting. In contrast, the samples with S-rich apatite have elevated La/Yb ratios of 49 ± 15 (1σ), zircon 10000*(Eu/EuN*)/Yb ratios of 26 ± 7 (1σ), and zircon δ18O values of 5.8 ± 0.1 ‰ (1σ), consistent with a deep, hydrous and homogeneous mantle-like source for the melts dominated by amphibole ± garnet fractionation that is reminiscent of subduction-like process. These are the first reported results documenting the predominant accommodation of relatively reduced S in S-rich apatite grains crystallized from terrestrial silicate melts, possibly reflecting slight oxidation associated with the hydration of Neoarchean mantle and crystal fractionation over the magma evolution. The more common S-poor apatite data suggest that suppressed oxidation of the parental sodic magmas led to weak S emission from Earth’s interior to its evolving surface, explaining the rarity of porphyry-type Cu deposits in > 2.7 Ga Archean sodic volcanoplutonic terranes.
期刊介绍:
ACS Applied Bio Materials is an interdisciplinary journal publishing original research covering all aspects of biomaterials and biointerfaces including and beyond the traditional biosensing, biomedical and therapeutic applications.
The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrates knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important bio applications. The journal is specifically interested in work that addresses the relationship between structure and function and assesses the stability and degradation of materials under relevant environmental and biological conditions.