Li-Ping Zeng , Carl Spandler , Ying-Ying Liu , Johannes Hammerli , Wang Liao , Hao Hu , Sanna Olsson , De-Xian Zhang , Tao He , Jian-Wei Li , Xin-Fu Zhao
{"title":"蒸发岩在瑞典北部北博滕地区基鲁纳型氧化铁磷灰石矿床中的作用:来自镰状石原位卤素分析的证据","authors":"Li-Ping Zeng , Carl Spandler , Ying-Ying Liu , Johannes Hammerli , Wang Liao , Hao Hu , Sanna Olsson , De-Xian Zhang , Tao He , Jian-Wei Li , Xin-Fu Zhao","doi":"10.1016/j.chemgeo.2025.123009","DOIUrl":null,"url":null,"abstract":"<div><div>Hydrosaline liquids or salt melts have recently been suggested to play a key role in forming Kiruna-type iron oxide-apatite (IOA) deposits, with sedimentary evaporites proposed as contributors to ore-forming processes. However, the timing and role of evaporites in ore formation are poorly understood. Scapolite minerals, typical products of sodic alteration resulting from the interaction between hydrosaline liquids (also called highly saline fluids) and country rocks, may provide key insights into ore genesis. Here, we measured in situ Cl/Br ratios of scapolite from two representative IOA deposits (Mertainen and Gruvberget-Fe) and the Aitik porphyry Cu system from the Northern Norrbotten region of Sweden to trace the sources and evolution of ore-related liquids. Based on mineral assemblages, scapolite grains are classified into Scp I and Scp II. Scp I, formed during pre-ore or <em>syn</em>-ore alteration, exhibits distinct molar Cl/Br ratios (510–2000) across domains and grains. This variation implies multiple, though dominantly magmatic, sources for the associated liquids. Zoned Scp I crystals show relatively low molar Cl/Br ratios of 510–790 in their cores, increasing to 730–1640 in the mantles and/or rims. This trend suggests that the grains initially equilibrated with dominantly pore waters (bittern brines and/or seawater) but were later primarily buffered by liquids of magmatic origin. Scp II, associated with hematitization, have much higher molar Cl/Br ratios (2300–3500) and likely precipitated from halite-bearing evaporite-dissolution fluids derived from the Kiruna Greenstone Group. Our findings suggest that evaporite components were introduced into the studied IOA systems primarily through fluid circulation triggered by magmatic intrusion. However, later-stage evaporite dissolution fluids overprinting the ore system may create the misleading impression that evaporite-derived fluids played a key role in ore genesis.</div></div>","PeriodicalId":9847,"journal":{"name":"Chemical Geology","volume":"694 ","pages":"Article 123009"},"PeriodicalIF":3.6000,"publicationDate":"2025-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The role of evaporites in Kiruna-type iron oxide-apatite deposits in the Northern Norrbotten region, Sweden: Evidence from in situ halogen analyses of scapolite\",\"authors\":\"Li-Ping Zeng , Carl Spandler , Ying-Ying Liu , Johannes Hammerli , Wang Liao , Hao Hu , Sanna Olsson , De-Xian Zhang , Tao He , Jian-Wei Li , Xin-Fu Zhao\",\"doi\":\"10.1016/j.chemgeo.2025.123009\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Hydrosaline liquids or salt melts have recently been suggested to play a key role in forming Kiruna-type iron oxide-apatite (IOA) deposits, with sedimentary evaporites proposed as contributors to ore-forming processes. However, the timing and role of evaporites in ore formation are poorly understood. Scapolite minerals, typical products of sodic alteration resulting from the interaction between hydrosaline liquids (also called highly saline fluids) and country rocks, may provide key insights into ore genesis. Here, we measured in situ Cl/Br ratios of scapolite from two representative IOA deposits (Mertainen and Gruvberget-Fe) and the Aitik porphyry Cu system from the Northern Norrbotten region of Sweden to trace the sources and evolution of ore-related liquids. Based on mineral assemblages, scapolite grains are classified into Scp I and Scp II. Scp I, formed during pre-ore or <em>syn</em>-ore alteration, exhibits distinct molar Cl/Br ratios (510–2000) across domains and grains. This variation implies multiple, though dominantly magmatic, sources for the associated liquids. Zoned Scp I crystals show relatively low molar Cl/Br ratios of 510–790 in their cores, increasing to 730–1640 in the mantles and/or rims. This trend suggests that the grains initially equilibrated with dominantly pore waters (bittern brines and/or seawater) but were later primarily buffered by liquids of magmatic origin. Scp II, associated with hematitization, have much higher molar Cl/Br ratios (2300–3500) and likely precipitated from halite-bearing evaporite-dissolution fluids derived from the Kiruna Greenstone Group. Our findings suggest that evaporite components were introduced into the studied IOA systems primarily through fluid circulation triggered by magmatic intrusion. 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The role of evaporites in Kiruna-type iron oxide-apatite deposits in the Northern Norrbotten region, Sweden: Evidence from in situ halogen analyses of scapolite
Hydrosaline liquids or salt melts have recently been suggested to play a key role in forming Kiruna-type iron oxide-apatite (IOA) deposits, with sedimentary evaporites proposed as contributors to ore-forming processes. However, the timing and role of evaporites in ore formation are poorly understood. Scapolite minerals, typical products of sodic alteration resulting from the interaction between hydrosaline liquids (also called highly saline fluids) and country rocks, may provide key insights into ore genesis. Here, we measured in situ Cl/Br ratios of scapolite from two representative IOA deposits (Mertainen and Gruvberget-Fe) and the Aitik porphyry Cu system from the Northern Norrbotten region of Sweden to trace the sources and evolution of ore-related liquids. Based on mineral assemblages, scapolite grains are classified into Scp I and Scp II. Scp I, formed during pre-ore or syn-ore alteration, exhibits distinct molar Cl/Br ratios (510–2000) across domains and grains. This variation implies multiple, though dominantly magmatic, sources for the associated liquids. Zoned Scp I crystals show relatively low molar Cl/Br ratios of 510–790 in their cores, increasing to 730–1640 in the mantles and/or rims. This trend suggests that the grains initially equilibrated with dominantly pore waters (bittern brines and/or seawater) but were later primarily buffered by liquids of magmatic origin. Scp II, associated with hematitization, have much higher molar Cl/Br ratios (2300–3500) and likely precipitated from halite-bearing evaporite-dissolution fluids derived from the Kiruna Greenstone Group. Our findings suggest that evaporite components were introduced into the studied IOA systems primarily through fluid circulation triggered by magmatic intrusion. However, later-stage evaporite dissolution fluids overprinting the ore system may create the misleading impression that evaporite-derived fluids played a key role in ore genesis.
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.