Wen-Han Lo, Chin-Ho Tsai, Ioannis Baziotis, Sun-Lin Chung, Chiao Liu, Yoshiyuki Iizuka, Hao-Yang Lee
{"title":"块岩化学对台湾玉丽变质带高压绿帘石角闪岩中paragonite稳定性的影响","authors":"Wen-Han Lo, Chin-Ho Tsai, Ioannis Baziotis, Sun-Lin Chung, Chiao Liu, Yoshiyuki Iizuka, Hao-Yang Lee","doi":"10.1007/s00410-025-02228-2","DOIUrl":null,"url":null,"abstract":"<div><p>Paragonite is an important high-pressure (H<i>P</i>) indicator in epidote-amphibolites; however, its occurrence in these rocks is notably rare. Paragonite-bearing and paragonite-free epidote-amphibolites from Taiwan offer a great opportunity to understand the influence of bulk-rock chemistry on paragonite stability by phase equilibrium modelling. The investigated epidote-amphibolites have basaltic compositions with elevated Al₂O₃ content (16.2–19.7 wt%). The paragonite-bearing (PEA) type is characterised by pargasitic hornblende + epidote + paragonite + rutile + quartz ± garnet assemblages, while the paragonite-free (EA) type contains pargasitic hornblende + epidote + rutile + quartz ± chlorite assemblages. The mineralogical difference between the two types is attributed to a variation in bulk-rock Mg# (PEA: 28–54; EA: 63–67). Both types experienced similar peak pressure–temperature (<i>P–T</i>) conditions at 1.2–1.6 GPa and 575–625 °C (M1 stage). Although the <i>P–T</i> estimates are comparable to that of some eclogites, these rocks do not exhibit eclogite facies mineral assemblages. The corresponding paleo-geothermal gradients of 12–16 °C km<sup>− 1</sup> indicate a warm subduction environment, likely reflecting the thermal structure of a young intra-oceanic subduction zone. Although these rocks show little or no retrogression, we still identified two post-peak metamorphic stages, including a blueschist facies overprint at 0.7–0.8 GPa and 440–475 °C (M2 stage), and a greenschist facies overprint at 0.4–0.6 GPa and 400–475 °C (M3 stage). These <i>P–T</i> estimates suggest a cooling and decompression from M1 to M2, followed by a near isothermal decompression from M2 to M3. <i>P–T–X</i> modelling in the MnNCFMASHTO (K-free) systems shows that paragonite preferentially stabilises in high-Al, high-Na/(Na + Ca), high-Fe³⁺/ΣFe, or low-Mg# metabasic compositions. H₂O saturation, or near H₂O saturation, is also essential for paragonite stability. Using the median worldwide metabasite composition in Forshaw et al. (2024) as a global reference, the <i>P–X</i> modelling in the NCFMASHTO (K-free) system predicts that paragonite is stable when any one compositional parameter meets the following approximate thresholds: Al₂O₃ > ~17.0 wt%, Na/(Na + Ca) > ~ 0.45, or Fe³⁺/ΣFe > ~ 0.50. However, these values should be considered as a first-order approximation, rather than strict criteria. Our results emphasise the pivotal role of bulk-rock chemistry in controlling the occurrence of paragonite in metabasites.</p></div>","PeriodicalId":526,"journal":{"name":"Contributions to Mineralogy and Petrology","volume":"180 6","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2025-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effects of bulk-rock chemistry on paragonite stability in high-pressure epidote-amphibolites from the Yuli metamorphic belt, Taiwan\",\"authors\":\"Wen-Han Lo, Chin-Ho Tsai, Ioannis Baziotis, Sun-Lin Chung, Chiao Liu, Yoshiyuki Iizuka, Hao-Yang Lee\",\"doi\":\"10.1007/s00410-025-02228-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Paragonite is an important high-pressure (H<i>P</i>) indicator in epidote-amphibolites; however, its occurrence in these rocks is notably rare. Paragonite-bearing and paragonite-free epidote-amphibolites from Taiwan offer a great opportunity to understand the influence of bulk-rock chemistry on paragonite stability by phase equilibrium modelling. The investigated epidote-amphibolites have basaltic compositions with elevated Al₂O₃ content (16.2–19.7 wt%). The paragonite-bearing (PEA) type is characterised by pargasitic hornblende + epidote + paragonite + rutile + quartz ± garnet assemblages, while the paragonite-free (EA) type contains pargasitic hornblende + epidote + rutile + quartz ± chlorite assemblages. The mineralogical difference between the two types is attributed to a variation in bulk-rock Mg# (PEA: 28–54; EA: 63–67). Both types experienced similar peak pressure–temperature (<i>P–T</i>) conditions at 1.2–1.6 GPa and 575–625 °C (M1 stage). Although the <i>P–T</i> estimates are comparable to that of some eclogites, these rocks do not exhibit eclogite facies mineral assemblages. The corresponding paleo-geothermal gradients of 12–16 °C km<sup>− 1</sup> indicate a warm subduction environment, likely reflecting the thermal structure of a young intra-oceanic subduction zone. Although these rocks show little or no retrogression, we still identified two post-peak metamorphic stages, including a blueschist facies overprint at 0.7–0.8 GPa and 440–475 °C (M2 stage), and a greenschist facies overprint at 0.4–0.6 GPa and 400–475 °C (M3 stage). These <i>P–T</i> estimates suggest a cooling and decompression from M1 to M2, followed by a near isothermal decompression from M2 to M3. <i>P–T–X</i> modelling in the MnNCFMASHTO (K-free) systems shows that paragonite preferentially stabilises in high-Al, high-Na/(Na + Ca), high-Fe³⁺/ΣFe, or low-Mg# metabasic compositions. H₂O saturation, or near H₂O saturation, is also essential for paragonite stability. Using the median worldwide metabasite composition in Forshaw et al. (2024) as a global reference, the <i>P–X</i> modelling in the NCFMASHTO (K-free) system predicts that paragonite is stable when any one compositional parameter meets the following approximate thresholds: Al₂O₃ > ~17.0 wt%, Na/(Na + Ca) > ~ 0.45, or Fe³⁺/ΣFe > ~ 0.50. However, these values should be considered as a first-order approximation, rather than strict criteria. Our results emphasise the pivotal role of bulk-rock chemistry in controlling the occurrence of paragonite in metabasites.</p></div>\",\"PeriodicalId\":526,\"journal\":{\"name\":\"Contributions to Mineralogy and Petrology\",\"volume\":\"180 6\",\"pages\":\"\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2025-05-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Contributions to Mineralogy and Petrology\",\"FirstCategoryId\":\"89\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s00410-025-02228-2\",\"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}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Contributions to Mineralogy and Petrology","FirstCategoryId":"89","ListUrlMain":"https://link.springer.com/article/10.1007/s00410-025-02228-2","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}
Effects of bulk-rock chemistry on paragonite stability in high-pressure epidote-amphibolites from the Yuli metamorphic belt, Taiwan
Paragonite is an important high-pressure (HP) indicator in epidote-amphibolites; however, its occurrence in these rocks is notably rare. Paragonite-bearing and paragonite-free epidote-amphibolites from Taiwan offer a great opportunity to understand the influence of bulk-rock chemistry on paragonite stability by phase equilibrium modelling. The investigated epidote-amphibolites have basaltic compositions with elevated Al₂O₃ content (16.2–19.7 wt%). The paragonite-bearing (PEA) type is characterised by pargasitic hornblende + epidote + paragonite + rutile + quartz ± garnet assemblages, while the paragonite-free (EA) type contains pargasitic hornblende + epidote + rutile + quartz ± chlorite assemblages. The mineralogical difference between the two types is attributed to a variation in bulk-rock Mg# (PEA: 28–54; EA: 63–67). Both types experienced similar peak pressure–temperature (P–T) conditions at 1.2–1.6 GPa and 575–625 °C (M1 stage). Although the P–T estimates are comparable to that of some eclogites, these rocks do not exhibit eclogite facies mineral assemblages. The corresponding paleo-geothermal gradients of 12–16 °C km− 1 indicate a warm subduction environment, likely reflecting the thermal structure of a young intra-oceanic subduction zone. Although these rocks show little or no retrogression, we still identified two post-peak metamorphic stages, including a blueschist facies overprint at 0.7–0.8 GPa and 440–475 °C (M2 stage), and a greenschist facies overprint at 0.4–0.6 GPa and 400–475 °C (M3 stage). These P–T estimates suggest a cooling and decompression from M1 to M2, followed by a near isothermal decompression from M2 to M3. P–T–X modelling in the MnNCFMASHTO (K-free) systems shows that paragonite preferentially stabilises in high-Al, high-Na/(Na + Ca), high-Fe³⁺/ΣFe, or low-Mg# metabasic compositions. H₂O saturation, or near H₂O saturation, is also essential for paragonite stability. Using the median worldwide metabasite composition in Forshaw et al. (2024) as a global reference, the P–X modelling in the NCFMASHTO (K-free) system predicts that paragonite is stable when any one compositional parameter meets the following approximate thresholds: Al₂O₃ > ~17.0 wt%, Na/(Na + Ca) > ~ 0.45, or Fe³⁺/ΣFe > ~ 0.50. However, these values should be considered as a first-order approximation, rather than strict criteria. Our results emphasise the pivotal role of bulk-rock chemistry in controlling the occurrence of paragonite in metabasites.
期刊介绍:
Contributions to Mineralogy and Petrology is an international journal that accepts high quality research papers in the fields of igneous and metamorphic petrology, geochemistry and mineralogy.
Topics of interest include: major element, trace element and isotope geochemistry, geochronology, experimental petrology, igneous and metamorphic petrology, mineralogy, major and trace element mineral chemistry and thermodynamic modeling of petrologic and geochemical processes.