Pub Date : 2024-06-03DOI: 10.1007/s11631-024-00707-0
Jiamei Li, Yu-Yan Sara Zhao, He Cui, Shuai-Yi Qu, Yanhua Peng, Yuhong Yang, Xiongyao Li
Perchlorate and chlorate are present in various extraterrestrial celestial bodies throughout the solar system, such as Mars, the moon, and asteroids. To date, the origin mechanisms of perchlorate and chlorate on the Martian surface have been well-established; however, relatively little attention has been cast to airless bodies. Here, we experimentally investigated the potential oxidation mechanisms of chloride to chlorate and perchlorate, such as ultraviolet irradiation under H2O- and O2-free conditions and mechanical pulverization processes. Individual minerals, olivine, pyroxene, ilmenite, magnetite, TiO2 and anhydrous ferric sulfate, and lunar regolith simulants (low Ti, CLRS-1; high-Ti, CLRS-2) and their metallic iron (Fe0) bearing counterparts were examined. We found that pulverization of dry matrix material-halite mixtures, even in the presence of O2, does not necessarily lead to perchlorate and chlorate formation without involving water. Under photocatalytic and H2O- and O2-free conditions, olivine and pyroxene can produce oxychlorine (ClOx−) species, although the yields were orders of magnitude lower than those under Martian-relevant conditions. Nanophase-Fe0 particles in the lunar regolith and the common photocatalyst TiO2 can facilitate the ClOx− formation, but their yields were lower than those with olivine. The oxides ilmenite and magnetite did not efficiently contribute to ClOx− production. Our results highlight the critical role of H2O in the oxidation chloride to chlorate and perchlorate, and provide essential insights into the environmental influence on the formation of oxychlorine species on different celestial bodies.
{"title":"Experimental constraints on the formation of oxychlorine species by UV irradiation and mechanical pulverization on the lunar surface","authors":"Jiamei Li, Yu-Yan Sara Zhao, He Cui, Shuai-Yi Qu, Yanhua Peng, Yuhong Yang, Xiongyao Li","doi":"10.1007/s11631-024-00707-0","DOIUrl":"10.1007/s11631-024-00707-0","url":null,"abstract":"<div><p>Perchlorate and chlorate are present in various extraterrestrial celestial bodies throughout the solar system, such as Mars, the moon, and asteroids. To date, the origin mechanisms of perchlorate and chlorate on the Martian surface have been well-established; however, relatively little attention has been cast to airless bodies. Here, we experimentally investigated the potential oxidation mechanisms of chloride to chlorate and perchlorate, such as ultraviolet irradiation under H<sub>2</sub>O- and O<sub>2</sub>-free conditions and mechanical pulverization processes. Individual minerals, olivine, pyroxene, ilmenite, magnetite, TiO<sub>2</sub> and anhydrous ferric sulfate, and lunar regolith simulants (low Ti, CLRS-1; high-Ti, CLRS-2) and their metallic iron (Fe<sup>0</sup>) bearing counterparts were examined. We found that pulverization of dry matrix material-halite mixtures, even in the presence of O<sub>2</sub>, does not necessarily lead to perchlorate and chlorate formation without involving water. Under photocatalytic and H<sub>2</sub>O- and O<sub>2</sub>-free conditions, olivine and pyroxene can produce oxychlorine (ClO<sub>x</sub><sup>−</sup>) species, although the yields were orders of magnitude lower than those under Martian-relevant conditions. Nanophase-Fe<sup>0</sup> particles in the lunar regolith and the common photocatalyst TiO<sub>2</sub> can facilitate the ClO<sub>x</sub><sup>−</sup> formation, but their yields were lower than those with olivine. The oxides ilmenite and magnetite did not efficiently contribute to ClO<sub>x</sub><sup>−</sup> production. Our results highlight the critical role of H<sub>2</sub>O in the oxidation chloride to chlorate and perchlorate, and provide essential insights into the environmental influence on the formation of oxychlorine species on different celestial bodies.</p></div>","PeriodicalId":7151,"journal":{"name":"Acta Geochimica","volume":"43 4","pages":"625 - 637"},"PeriodicalIF":1.4,"publicationDate":"2024-06-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141269227","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Research on the origin of carbonates in Changdu Basin holds significant importance for understanding the regional potash formation model. Based on a comprehensive review of previous studies, field geological surveys, and laboratory investigations, this study analyzes the origin and properties of carbonates within the context of regional potash formation. Petrographic studies show that magnesite deposits, with the characteristics of sedimentary origin. The results of elemental geochemical analysis show that the carbonates in this area were formed in the sedimentary environment via evaporation followed by concentration, and the formation of magnesite was possibly caused by the substitution of calcium in the dolomite with magnesium-rich brine. The δ13C values of carbonats in the study area are between 5.9‰ and 9.1‰. The δ18O values of magnesite samples range from − 7.3‰ to − 1.3‰, and the δ18O values of dolomites range from − 10.3‰ to − 8.4‰. All the calculated Z values of oxygen isotopes of carbonates greater than 120. A comprehensive analysis of carbon and oxygen isotopes indicates that the magnesite was formed in a highly concentrated Marine sedimentary environment and does not show any relation with the metasomatism of hydrothermal fluids. The results on the correlation of magnesite with seawater and its sedimentary origin provide key information for explaining the migration direction of brine between the Changdu and Lanping–Simao Basins. The residual metamorphic seawater in the Changdu Basin migrated to the Lanping–Simao Basin, where potash underwent deposition. Whereas, magnesite and dolomite in the early stage of potash formation were left in the Changdu Basin.
昌都盆地碳酸盐岩的成因研究对于理解区域钾盐形成模式具有重要意义。本研究在全面回顾以往研究、野外地质调查和实验室研究的基础上,分析了区域钾盐形成背景下碳酸盐岩的成因和性质。岩石学研究表明,菱镁矿沉积具有沉积成因的特征。元素地球化学分析结果表明,该地区的碳酸盐是在沉积环境中通过蒸发后浓缩形成的,而菱镁矿的形成可能是由于白云岩中的钙被富含镁的盐水所取代。研究区域碳酸盐岩的δ13C值介于5.9‰和9.1‰之间。菱镁矿样品的δ18O值介于-7.3‰至-1.3‰之间,白云岩的δ18O值介于-10.3‰至-8.4‰之间。所有计算得出的碳酸盐氧同位素 Z 值均大于 120。碳和氧同位素的综合分析表明,菱镁矿是在高浓度海洋沉积环境中形成的,与热液的变质作用没有任何关系。菱镁矿与海水的相关性及其沉积成因的研究结果为解释盐水在昌都盆地和兰坪-思茅盆地之间的迁移方向提供了关键信息。昌都盆地的残余变质海水向兰坪-思茅盆地迁移,钾盐在此沉积。而钾盐形成初期的菱镁矿和白云岩则留在了昌都盆地。
{"title":"Genesis and geological significance of carbonate in Changdu Basin, Xizang, China: Constraints from geochemistry and C–O isotopes","authors":"Wenhua Han, Yongshou Li, Haizhou Ma, Huaide Cheng, Binkai Li, Qinyu Hai, Xuahai Ma","doi":"10.1007/s11631-024-00704-3","DOIUrl":"10.1007/s11631-024-00704-3","url":null,"abstract":"<div><p>Research on the origin of carbonates in Changdu Basin holds significant importance for understanding the regional potash formation model. Based on a comprehensive review of previous studies, field geological surveys, and laboratory investigations, this study analyzes the origin and properties of carbonates within the context of regional potash formation. Petrographic studies show that magnesite deposits, with the characteristics of sedimentary origin. The results of elemental geochemical analysis show that the carbonates in this area were formed in the sedimentary environment via evaporation followed by concentration, and the formation of magnesite was possibly caused by the substitution of calcium in the dolomite with magnesium-rich brine. The δ<sup>13</sup>C values of carbonats in the study area are between 5.9‰ and 9.1‰. The δ<sup>18</sup>O values of magnesite samples range from − 7.3‰ to − 1.3‰, and the δ<sup>18</sup>O values of dolomites range from − 10.3‰ to − 8.4‰. All the calculated Z values of oxygen isotopes of carbonates greater than 120. A comprehensive analysis of carbon and oxygen isotopes indicates that the magnesite was formed in a highly concentrated Marine sedimentary environment and does not show any relation with the metasomatism of hydrothermal fluids. The results on the correlation of magnesite with seawater and its sedimentary origin provide key information for explaining the migration direction of brine between the Changdu and Lanping–Simao Basins. The residual metamorphic seawater in the Changdu Basin migrated to the Lanping–Simao Basin, where potash underwent deposition. Whereas, magnesite and dolomite in the early stage of potash formation were left in the Changdu Basin.</p></div>","PeriodicalId":7151,"journal":{"name":"Acta Geochimica","volume":"43 6","pages":"1192 - 1204"},"PeriodicalIF":1.4,"publicationDate":"2024-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142664453","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-05-23DOI: 10.1007/s11631-024-00701-6
Vladimir N. Kuleshov, Andrey Yu. Bychkov, Irina Yu. Nikolaeva, Maria E. Tarnopolskaia
Chemical (REE and major elements) and isotope (δ13C, δ18O) composition of carbonate manganese ores and manganese-bearing carbonates of the Usa deposit (Siberia, Russia) were studied. Received data on the composition of REE exhibit both the distinct negative (Ce/Ce*PAAS < 1) and positive (Ce/Ce*PAAS˃1) cerium anomalies and the positive Eu-anomaly (Eu/Eu*PAAS˃1). Negative Eu-anomalies are not observed. The contents of Mn, Fe, REE, and Ce-anomalies show a positive correlation with each other. Ce-anomalies and the amount of manganese and REE in relation to the carbon isotope composition (δ13C) show a negative relationship and indicate that oxidized carbon of organic matter played an important role in the concentration of manganese and REE in manganese ores. The chemical and isotope composition of examined rocks indicates on secondary formation of Mn-ores. Two major phases and sources are distinguished in the ore-forming process characterized by different chemical (REE and ore elements) and isotope composition: (i) high-grade manganese ores (with high contents of REE and light carbon isotope composition) and (ii) low-grade manganese ores (with low contents of REE and heavy carbon isotope composition).
研究了乌萨矿床(俄罗斯西伯利亚)碳酸盐锰矿和含锰碳酸盐的化学(REE和主要元素)和同位素(δ13C、δ18O)组成。所收到的有关 REE 成分的数据显示出明显的负(Ce/Ce*PAAS <1)和正(Ce/Ce*PAAS˃1)铈异常以及正 Eu 异常(Eu/Eu*PAAS˃1)。未观察到负 Eu 异常。锰、铁、稀土元素和铈异常的含量呈正相关。锰、铁、REE和C-异常的含量与碳同位素组成(δ13C)呈负相关,表明有机质的氧化碳对锰矿石中锰、REE的富集起着重要作用。所考察岩石的化学成分和同位素组成表明锰矿是二次形成的。在矿石形成过程中,有两个主要阶段和来源,它们具有不同的化学(REE和矿石元素)和同位素组成:(i)高品位锰矿石(REE和轻碳同位素组成含量高)和(ii)低品位锰矿石(REE和重碳同位素组成含量低)。
{"title":"Catagenetic type of manganese ores: REE and isotope (δ13C, δ18O) geochemical features (on the example of the Usa deposit, Russia)","authors":"Vladimir N. Kuleshov, Andrey Yu. Bychkov, Irina Yu. Nikolaeva, Maria E. Tarnopolskaia","doi":"10.1007/s11631-024-00701-6","DOIUrl":"10.1007/s11631-024-00701-6","url":null,"abstract":"<div><p>Chemical (REE and major elements) and isotope (δ<sup>13</sup>C, δ<sup>18</sup>O) composition of carbonate manganese ores and manganese-bearing carbonates of the Usa deposit (Siberia, Russia) were studied. Received data on the composition of REE exhibit both the distinct negative (Ce/Ce*<sub>PAAS</sub> < 1) and positive (Ce/Ce*<sub>PAAS</sub>˃1) cerium anomalies and the positive Eu-anomaly (Eu/Eu*<sub>PAAS</sub>˃1). Negative Eu-anomalies are not observed. The contents of Mn, Fe, REE, and Ce-anomalies show a positive correlation with each other. Ce-anomalies and the amount of manganese and REE in relation to the carbon isotope composition (δ<sup>13</sup>C) show a negative relationship and indicate that oxidized carbon of organic matter played an important role in the concentration of manganese and REE in manganese ores. The chemical and isotope composition of examined rocks indicates on secondary formation of Mn-ores. Two major phases and sources are distinguished in the ore-forming process characterized by different chemical (REE and ore elements) and isotope composition: (i) high-grade manganese ores (with high contents of REE and light carbon isotope composition) and (ii) low-grade manganese ores (with low contents of REE and heavy carbon isotope composition).</p></div>","PeriodicalId":7151,"journal":{"name":"Acta Geochimica","volume":"43 6","pages":"1133 - 1152"},"PeriodicalIF":1.4,"publicationDate":"2024-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141107604","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Rice (Oryza sativa L.) paddies are increasingly threatened by cadmium (Cd) pollution, and potentially serve as CH4 emitters to the atmosphere. Remediation agents widely mitigate Cd pollution in paddy soil, however, we know little about their regulations on CH4 emission. Here, via adding biochar (B), sulfhydryl-modified palygorskite (SMP), and selenium foliar fertilizer (SFF), we conducted a pot experiment to investigate soil and rice Cd contents together with in-situ CH4 fluxes. Compared to CK, the addition of SMP, SFF, and B-SMP reduced Cd in brown rice by 25% to 50%, 25%, and 50% to 75%, respectively. Agents 7% B, 7% B-0.01% SMP, and SFF reduced CH4 emissions by 8.46%, 5.30%, and 4.11%, respectively. CH4 emission increased gradually along the growing season, with the cumulative CH4 fluxes ranging between 338.82 and 619.13 kg hm−2. Our results highlight that mixed 7% B-0.01% SMP and SFF showed collaborative effects on Cd remediation and CH4 emission. This study reveals the feasibility of reducing Cd pollution and CH4 emission in karst rice paddies, which hopes to supplement the knowledge of collaborative controls on soil remediation and carbon emission.
{"title":"Can soil remediation agents synergistically mitigate rice Cd content and CH4 emission from karst paddies?","authors":"Wangbiao Lu, Guangneng Zeng, Weijun Luo, Jiangju Song, Maofei Ni, Shuangqin Guo, Qi Zhang, Chengling Huang, Cheng Yang, Haijun Du, Shijie Wang","doi":"10.1007/s11631-024-00696-0","DOIUrl":"10.1007/s11631-024-00696-0","url":null,"abstract":"<div><p>Rice (<i>Oryza sativa</i> L.) paddies are increasingly threatened by cadmium (Cd) pollution, and potentially serve as CH<sub>4</sub> emitters to the atmosphere. Remediation agents widely mitigate Cd pollution in paddy soil, however, we know little about their regulations on CH<sub>4</sub> emission. Here, via adding biochar (B), sulfhydryl-modified palygorskite (SMP), and selenium foliar fertilizer (SFF), we conducted a pot experiment to investigate soil and rice Cd contents together with <i>in</i>-<i>situ</i> CH<sub>4</sub> fluxes. Compared to CK, the addition of SMP, SFF, and B-SMP reduced Cd in brown rice by 25% to 50%, 25%, and 50% to 75%, respectively. Agents 7% B, 7% B-0.01% SMP, and SFF reduced CH<sub>4</sub> emissions by 8.46%, 5.30%, and 4.11%, respectively. CH<sub>4</sub> emission increased gradually along the growing season, with the cumulative CH<sub>4</sub> fluxes ranging between 338.82 and 619.13 kg hm<sup>−2</sup>. Our results highlight that mixed 7% B-0.01% SMP and SFF showed collaborative effects on Cd remediation and CH<sub>4</sub> emission. This study reveals the feasibility of reducing Cd pollution and CH<sub>4</sub> emission in karst rice paddies, which hopes to supplement the knowledge of collaborative controls on soil remediation and carbon emission.</p></div>","PeriodicalId":7151,"journal":{"name":"Acta Geochimica","volume":"43 6","pages":"1123 - 1132"},"PeriodicalIF":1.4,"publicationDate":"2024-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141106762","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-05-21DOI: 10.1007/s11631-024-00703-4
Xiande Xie, Xiangping Gu, Yiping Yang
Copper possesses very strong chacophile properties, but under the conditions found in meteorites, its behavior is like that of siderophile elements. The Suizhou meteorite is a highly shocked L6 chondrite. Troilite and taenite are considered the main primary carrier of copper in this meteorite, and the post-shock thermal episode is considered the main reason that elemental Cu migrates from its original host phase and forms metallic grains. The Suizhou meteorite contains a few very thin shock melt veins. The occurrence and behavior of metallic copper in this meteorite were studied by optical microscopic examination, electron microprobe analyses, and high-resolution X-ray elemental intensity mapping. Our results show that metallic copper is abundant in the Suizhou chondritic rock. Metallic copper grains adjacent to small troilite grains inside FeNi metal are the most common occurrence, and those at the FeNi metal–troilite interface are the second most common case. The metallic copper grains occurring at the interface of FeNi metal/troililte and silicate are rather rare. Metallic copper grains are not observed within the Suizhou shock veins, Instead, Cu in elemental form is transferred through shock metamorphism into FeNi metal + troilite intergrowths. Four different occurrence types of Cu in the FeNi metal + troilite intergrowths have been identified: the concentrations of Cu in the FeNi + FeS intergrowths for four occurrence types are rather close, we estimate it might be lower than 1 wt%.
铜具有很强的嗜铬性,但在陨石中发现的条件下,其行为与嗜硒元素相似。随州陨石是一块高度休克的 L6 型陨石。冲击后的热效应被认为是铜元素从其原始主相迁移并形成金属颗粒的主要原因。随州陨石含有几条很细的冲击熔脉。我们通过光学显微镜检查、电子微探针分析和高分辨率 X 射线元素强度图谱研究了这块陨石中金属铜的出现和行为。我们的研究结果表明,金属铜在随州陨石中含量丰富。金属铜粒最常出现在铁镍金属内部的小铁镍岩颗粒附近,其次是铁镍金属-铁镍岩界面上的金属铜粒。出现在金属镍/绿泥石和硅酸盐界面上的金属铜粒相当罕见。在随州冲击矿脉中没有观察到金属铜粒,相反,元素形式的铜通过冲击变质作用转移到铁镍金属+绿泥石互生层中。在铁镍金属+铁闪长岩互生体中发现了四种不同类型的铜:四种类型的铁镍+铁闪长岩互生体中铜的浓度相当接近,我们估计可能低于 1 wt%。
{"title":"The occurrence of metallic copper and redistribution of copper in the shocked Suizhou L6 chondrite","authors":"Xiande Xie, Xiangping Gu, Yiping Yang","doi":"10.1007/s11631-024-00703-4","DOIUrl":"10.1007/s11631-024-00703-4","url":null,"abstract":"<div><p>Copper possesses very strong chacophile properties, but under the conditions found in meteorites, its behavior is like that of siderophile elements. The Suizhou meteorite is a highly shocked L6 chondrite. Troilite and taenite are considered the main primary carrier of copper in this meteorite, and the post-shock thermal episode is considered the main reason that elemental Cu migrates from its original host phase and forms metallic grains. The Suizhou meteorite contains a few very thin shock melt veins. The occurrence and behavior of metallic copper in this meteorite were studied by optical microscopic examination, electron microprobe analyses, and high-resolution X-ray elemental intensity mapping. Our results show that metallic copper is abundant in the Suizhou chondritic rock. Metallic copper grains adjacent to small troilite grains inside FeNi metal are the most common occurrence, and those at the FeNi metal–troilite interface are the second most common case. The metallic copper grains occurring at the interface of FeNi metal/troililte and silicate are rather rare. Metallic copper grains are not observed within the Suizhou shock veins, Instead, Cu in elemental form is transferred through shock metamorphism into FeNi metal + troilite intergrowths. Four different occurrence types of Cu in the FeNi metal + troilite intergrowths have been identified: the concentrations of Cu in the FeNi + FeS intergrowths for four occurrence types are rather close, we estimate it might be lower than 1 wt%.</p></div>","PeriodicalId":7151,"journal":{"name":"Acta Geochimica","volume":"43 5","pages":"827 - 837"},"PeriodicalIF":1.4,"publicationDate":"2024-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141117539","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-05-21DOI: 10.1007/s11631-024-00699-x
Ronghua Pang, Yang Li, Chen Li, Pengfei Zhang, Zhuang Guo, Sizhe Zhao, Han Yu, Li Wang, Chenxi Zhu, Shuangyu Wang, Kairui Tai, Qinwei Zhang, Yuanyun Wen, Rui Li
Space weathering is a primary factor in altering the composition and spectral characteristics of surface materials on airless planets. However, current research on space weathering focuses mainly on the Moon and certain types of asteroids. In particular, the impacts of meteoroids and micrometeoroids, radiation from solar wind/solar flares/cosmic rays, and thermal fatigue due to temperature variations are being studied. Space weathering produces various transformation products such as melted glass, amorphous layers, iron particles, vesicles, and solar wind water. These in turn lead to soil maturation, changes in visible and near-infrared reflectance spectra (weakening of characteristic absorption peaks, decreased reflectance, increased near-infrared slope), and alterations in magnetism (related to small iron particles), collectively termed the “lunar model” of space weathering transformation. Compared to the Moon and asteroids, Mercury has unique spatial environmental characteristics, including more intense meteoroid impacts and solar thermal radiation, as well as a weaker particle radiation environment due to the global distribution of its magnetic field. Therefore, the lunar model of space weathering may not apply to Mercury. Previous studies have extensively explored the effects of micrometeoroid impacts. Hence, this work focuses on the effects of solar-wind particle radiation in global magnetic-field distribution and on the weathering transformation of surface materials on Mercury under prolonged intense solar irradiation. Through the utilization of high-valence state, heavy ion implantation, and vacuum heating simulation experiments, this paper primarily investigates the weathering transformation characteristics of the major mineral components such as anorthite, pyroxene, and olivine on Mercury's surface and compares them to the weathering transformation model of the Moon. The experimental results indicate that ion implantation at room temperature is insufficient to generate np-Fe0 directly but can facilitate its formation, while prolonged exposure to solar thermal radiation on Mercury's surface can lead directly to the formation of np-Fe0. Therefore, intense solar thermal radiation is a crucial component of the unique space weathering transformation process on Mercury's surface.
{"title":"Formation and growth of nanophase iron particles on the surface of Mercury revealed by experimental study","authors":"Ronghua Pang, Yang Li, Chen Li, Pengfei Zhang, Zhuang Guo, Sizhe Zhao, Han Yu, Li Wang, Chenxi Zhu, Shuangyu Wang, Kairui Tai, Qinwei Zhang, Yuanyun Wen, Rui Li","doi":"10.1007/s11631-024-00699-x","DOIUrl":"10.1007/s11631-024-00699-x","url":null,"abstract":"<div><p>Space weathering is a primary factor in altering the composition and spectral characteristics of surface materials on airless planets. However, current research on space weathering focuses mainly on the Moon and certain types of asteroids. In particular, the impacts of meteoroids and micrometeoroids, radiation from solar wind/solar flares/cosmic rays, and thermal fatigue due to temperature variations are being studied. Space weathering produces various transformation products such as melted glass, amorphous layers, iron particles, vesicles, and solar wind water. These in turn lead to soil maturation, changes in visible and near-infrared reflectance spectra (weakening of characteristic absorption peaks, decreased reflectance, increased near-infrared slope), and alterations in magnetism (related to small iron particles), collectively termed the “lunar model” of space weathering transformation. Compared to the Moon and asteroids, Mercury has unique spatial environmental characteristics, including more intense meteoroid impacts and solar thermal radiation, as well as a weaker particle radiation environment due to the global distribution of its magnetic field. Therefore, the lunar model of space weathering may not apply to Mercury. Previous studies have extensively explored the effects of micrometeoroid impacts. Hence, this work focuses on the effects of solar-wind particle radiation in global magnetic-field distribution and on the weathering transformation of surface materials on Mercury under prolonged intense solar irradiation. Through the utilization of high-valence state, heavy ion implantation, and vacuum heating simulation experiments, this paper primarily investigates the weathering transformation characteristics of the major mineral components such as anorthite, pyroxene, and olivine on Mercury's surface and compares them to the weathering transformation model of the Moon. The experimental results indicate that ion implantation at room temperature is insufficient to generate np-Fe<sup>0</sup> directly but can facilitate its formation, while prolonged exposure to solar thermal radiation on Mercury's surface can lead directly to the formation of np-Fe<sup>0</sup>. Therefore, intense solar thermal radiation is a crucial component of the unique space weathering transformation process on Mercury's surface.</p></div>","PeriodicalId":7151,"journal":{"name":"Acta Geochimica","volume":"43 4","pages":"774 - 784"},"PeriodicalIF":1.4,"publicationDate":"2024-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141114281","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-05-15DOI: 10.1007/s11631-024-00694-2
Hui Hou, Wei Cheng, Ruidong Yang, Yan Zhang
Coal seams can enrich a variety of harmful trace elements under specific geological conditions. The spatial distribution of harmful trace elements in coal is extremely uneven, and the distribution characteristics of each element content are different. The harmful elements released in the process of coal mining and utilization will cause serious harm to the environment and the human body. It is of great resource significance to study the geochemistry of coal that affects the enrichment and distribution characteristics of harmful trace elements. Based on the domestic and foreign literature on coal geochemistry in Guizhou published by previous investigators, this study counted 1097 sample data from 23 major coal-producing counties in Guizhou Province, systematically summarized the relevant research results of harmful trace elements in the coal of Guizhou, and revealed the overall distribution and enrichment characteristics of harmful trace elements in the coal of Guizhou. The results show that the average contents of Cd, Pb, Se, Cu, Mo, U, V, As, Hg, and Cr in coal of Guizhou are higher than those in Chinese coal and world coal. A variety of harmful trace elements in the coal of Guizhou have high background values, especially in Liupanshui, Xingyi and Qianbei coalfield. The enrichment of various harmful trace elements in the Late Permian coal in Guizhou is mainly related to the combined action of various geological and geochemical factors. The supply of terrigenous debris and sedimentary environment may be the basic background of the enrichment of harmful elements in western Guizhou, while low-temperature hydrothermal activity and volcanic ash deposition may be the main reasons for the enrichment of harmful elements in southwestern Guizhou.
{"title":"The abundance, distribution, and enrichment mechanism of harmful trace elements in coals from Guizhou, Southwestern China","authors":"Hui Hou, Wei Cheng, Ruidong Yang, Yan Zhang","doi":"10.1007/s11631-024-00694-2","DOIUrl":"10.1007/s11631-024-00694-2","url":null,"abstract":"<div><p>Coal seams can enrich a variety of harmful trace elements under specific geological conditions. The spatial distribution of harmful trace elements in coal is extremely uneven, and the distribution characteristics of each element content are different. The harmful elements released in the process of coal mining and utilization will cause serious harm to the environment and the human body. It is of great resource significance to study the geochemistry of coal that affects the enrichment and distribution characteristics of harmful trace elements. Based on the domestic and foreign literature on coal geochemistry in Guizhou published by previous investigators, this study counted 1097 sample data from 23 major coal-producing counties in Guizhou Province, systematically summarized the relevant research results of harmful trace elements in the coal of Guizhou, and revealed the overall distribution and enrichment characteristics of harmful trace elements in the coal of Guizhou. The results show that the average contents of Cd, Pb, Se, Cu, Mo, U, V, As, Hg, and Cr in coal of Guizhou are higher than those in Chinese coal and world coal. A variety of harmful trace elements in the coal of Guizhou have high background values, especially in Liupanshui, Xingyi and Qianbei coalfield. The enrichment of various harmful trace elements in the Late Permian coal in Guizhou is mainly related to the combined action of various geological and geochemical factors. The supply of terrigenous debris and sedimentary environment may be the basic background of the enrichment of harmful elements in western Guizhou, while low-temperature hydrothermal activity and volcanic ash deposition may be the main reasons for the enrichment of harmful elements in southwestern Guizhou.</p></div>","PeriodicalId":7151,"journal":{"name":"Acta Geochimica","volume":"43 5","pages":"889 - 903"},"PeriodicalIF":1.4,"publicationDate":"2024-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140976048","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The Chayong Cu-polymetallic deposit is a recently discovered Cu-polymetallic deposit hosted in the Sanjiang Metallogenic Belt within the Tibetan Plateau of China to the northeast of the North Qiangtang terrane. The ore body occurs in siltstone and is controlled by a northwest-trending fault structure. According to the associations, assemblages, and cutting relationships between ore veins, the hydrothermal mineralization period can be divided into three mineralization stages: (1) a molybdenite mineralization stage, (2) a Cu-polymetallic sulfide stage, and (3) a quartz-carbonate stage. Two types of fluid inclusions (FIs), namely, liquid and vapor-rich inclusions, are present in quartz associated with sulfide minerals. Early-stage FIs are both liquid and vapor-rich, homogenized at temperatures ranging from 364.1 to 384.2 °C, and have salinities ranging from 0.70% to 9.60% NaCl equivalent (eqv). The middle-stage FIs are also both liquid- and vapor-rich, homogenized at temperatures ranging from 272.4 to 355.6 °C, and have salinities ranging from 0.53%–17.10% NaCl eqv. The late-stage FIs are liquid, homogenized at temperatures ranging from 209.4 to 255.3 °C, and have salinities ranging from 0.35%–6.87% NaCl eqv. The samples from the deposit have δ34S values of − 21.8‰ to − 19.2‰ and − 5.5‰ to − 6.0‰, suggesting that sulfur was derived from the host sediments and magmatic fluids, respectively. The metallic minerals within the deposit have 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb values of 18.439–18.458, 15.656–15.679, and 38.772–38.863, respectively, suggesting that the metals were derived from the upper crust and orogenic belts. The samples from the deposit have δ18OW values of 2.99‰–7.99‰ and δDW values ranging from − 84.4‰ to − 73.9‰, indicating that the ore-forming fluids were magmatic and mixed with minor amounts of meteoric water. The ore-forming fluid of the Chayong copper polymetallic deposit was a high-temperature, medium- to low-salinity H2O–NaCl–CH4–N2 ± CO2 fluid system. The early high-temperature magmatic fluid, due to boiling, decreased in temperature, and via the mixing of meteoric water, gradually evolved towards the later-stage medium- to low-temperature and low-salinity fluid, causing molybdenite mineralization and forming copper polymetallic sulfide veins and quartz carbonate veins.
察雍铜多金属矿床是最近发现的一个铜多金属矿床,位于中国青藏高原三江成矿带,北羌塘地层东北部。矿体位于粉砂岩中,受西北走向断层构造控制。根据矿脉之间的关联、组合和切割关系,热液成矿期可分为三个成矿阶段:(1)辉钼矿成矿阶段;(2)铜多金属硫化物阶段;(3)石英碳酸盐阶段。与硫化物矿物伴生的石英中存在两种类型的流体包裹体(FIs),即液态包裹体和富汽态包裹体。早期阶段的流体包裹体既是液态的,也是富含蒸汽的,在 364.1 至 384.2 °C 的温度范围内均质,盐度介于 0.70% 至 9.60% NaCl 当量(当量)之间。中期陨石沉积物同样富含液体和蒸汽,在 272.4 至 355.6 °C 温度范围内均质,盐度范围为 0.53% 至 17.10% NaCl 当量。晚期 FI 为液态,在 209.4 至 255.3 °C 温度范围内均质,盐度范围为 0.35%-6.87% NaCl 当量。矿床样品的δ34S值分别为-21.8‰至-19.2‰和-5.5‰至-6.0‰,表明硫分别来源于寄主沉积物和岩浆流体。矿床内金属矿物的 206Pb/204Pb、207Pb/204Pb 和 208Pb/204Pb 值分别为 18.439-18.458、15.656-15.679 和 38.772-38.863,表明金属来源于上地壳和造山带。矿床样品的δ18OW值为2.99‰-7.99‰,δDW值为-84.4‰--73.9‰,表明成矿流体为岩浆流体,并混有少量陨石水。查永铜多金属矿床的成矿流体为高温、中低盐度的 H2O-NaCl-CH4-N2 ± CO2 流体体系。早期的高温岩浆流体由于沸腾,温度降低,通过陨水的混合,逐渐向后期的中低温低盐度流体演化,造成辉钼矿化,形成铜多金属硫化物矿脉和石英碳酸盐矿脉。
{"title":"Fluid inclusion and H-O-S-Pb isotope systematics of the Chayong Cu-polymetallic deposit, Sanjiang Metallogenic Belt, Qinghai Province, China","authors":"Jian Wang, Hao Wang, Fengyue Sun, Fei Wang, Xiangwen Li, Hongju Yue","doi":"10.1007/s11631-024-00700-7","DOIUrl":"10.1007/s11631-024-00700-7","url":null,"abstract":"<div><p>The Chayong Cu-polymetallic deposit is a recently discovered Cu-polymetallic deposit hosted in the Sanjiang Metallogenic Belt within the Tibetan Plateau of China to the northeast of the North Qiangtang terrane. The ore body occurs in siltstone and is controlled by a northwest-trending fault structure. According to the associations, assemblages, and cutting relationships between ore veins, the hydrothermal mineralization period can be divided into three mineralization stages: (1) a molybdenite mineralization stage, (2) a Cu-polymetallic sulfide stage, and (3) a quartz-carbonate stage. Two types of fluid inclusions (FIs), namely, liquid and vapor-rich inclusions, are present in quartz associated with sulfide minerals. Early-stage FIs are both liquid and vapor-rich, homogenized at temperatures ranging from 364.1 to 384.2 °C, and have salinities ranging from 0.70% to 9.60% NaCl equivalent (eqv). The middle-stage FIs are also both liquid- and vapor-rich, homogenized at temperatures ranging from 272.4 to 355.6 °C, and have salinities ranging from 0.53%–17.10% NaCl eqv. The late-stage FIs are liquid, homogenized at temperatures ranging from 209.4 to 255.3 °C, and have salinities ranging from 0.35%–6.87% NaCl eqv. The samples from the deposit have δ<sup>34</sup>S values of − 21.8‰ to − 19.2‰ and − 5.5‰ to − 6.0‰, suggesting that sulfur was derived from the host sediments and magmatic fluids, respectively. The metallic minerals within the deposit have <sup>206</sup>Pb/<sup>204</sup>Pb, <sup>207</sup>Pb/<sup>204</sup>Pb, and <sup>208</sup>Pb/<sup>204</sup>Pb values of 18.439–18.458, 15.656–15.679, and 38.772–38.863, respectively, suggesting that the metals were derived from the upper crust and orogenic belts. The samples from the deposit have δ<sup>18</sup>O<sub>W</sub> values of 2.99‰–7.99‰ and δD<sub>W</sub> values ranging from − 84.4‰ to − 73.9‰, indicating that the ore-forming fluids were magmatic and mixed with minor amounts of meteoric water. The ore-forming fluid of the Chayong copper polymetallic deposit was a high-temperature, medium- to low-salinity H<sub>2</sub>O–NaCl–CH<sub>4</sub>–N<sub>2</sub> ± CO<sub>2</sub> fluid system. The early high-temperature magmatic fluid, due to boiling, decreased in temperature, and via the mixing of meteoric water, gradually evolved towards the later-stage medium- to low-temperature and low-salinity fluid, causing molybdenite mineralization and forming copper polymetallic sulfide veins and quartz carbonate veins.</p></div>","PeriodicalId":7151,"journal":{"name":"Acta Geochimica","volume":"43 6","pages":"1153 - 1168"},"PeriodicalIF":1.4,"publicationDate":"2024-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141000864","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The Dahongshan Group, situated at the southwestern margin of the Yangtze Block, represents a geological unit characterized by relatively high-grade metamorphism in the region. This paper investigates the garnet-biotite schist from the Laochanghe Formation of the Dahongshan Group, employing an integrated approach that includes petrological analysis, phase equilibrium modeling, and zircon U–Pb dating. The schist is mainly composed of garnet, biotite, plagioclase, quartz, rutile, and ilmenite. Phase equilibrium modeling revealed the peak metamorphic conditions of 8–9 kbar and 635–675 °C. By further integrating the prograde metamorphic profile of garnet and geothermobarometric results, a clockwise P–T metamorphic evolution path is constructed, which includes an increase in temperature and pressure during the prograde stage. LA–ICP–MS zircon U–Pb dating and zircon Ti thermometry constrains the post-peak metamorphic age of 831.2 ± 7.2 Ma. Integrated with previously reported results, it is revealed that the southwestern margin of the Yangtze Block experienced a large-scale regional metamorphism during the Neoproterozoic (890–750 Ma), which is related to the collisional orogenic process. This may be associated with the late-stage assembly of the Rodinia supercontinent or with local compression and subduction processes during the breakup of the Rodinia supercontinent.
大洪山组位于扬子地块西南缘,是该地区具有较高品位变质作用的地质单元。本文采用岩石学分析、相平衡建模和锆石U-Pb定年等综合方法,研究了大洪山组老厂河地层的石榴石-生物岩片岩。片岩主要由石榴石、斜长石、斜长石、石英、金红石和钛铁矿组成。相平衡模型揭示了 8-9 kbar 和 635-675 °C 的峰值变质条件。通过进一步整合石榴石的顺行变质剖面和地温测压结果,构建了一条顺时针 P-T 变质演化路径,其中包括顺行阶段温度和压力的增加。LA-ICP-MS锆石U-Pb定年和锆石Ti测温法证实了831.2 ± 7.2 Ma的峰后变质年龄。结合之前报道的结果,揭示了扬子地块西南缘在新元古代(890-750 Ma)经历了大规模的区域变质作用,这与碰撞造山过程有关。这可能与罗迪尼亚超大陆晚期组装有关,也可能与罗迪尼亚超大陆解体过程中的局部压缩和俯冲过程有关。
{"title":"Metamorphic P–T conditions and ages of garnet-biotite schists in the Dahongshan Group from the southwestern Yangtze Block","authors":"Jun-xiao Ma, Guang-shu Yang, Yong-feng Yan, Xiao-Fei Xu, Yun-hua Ren, Hui Zhao, Xiao-jun Zheng, Yuan Qin","doi":"10.1007/s11631-024-00693-3","DOIUrl":"10.1007/s11631-024-00693-3","url":null,"abstract":"<div><p>The Dahongshan Group, situated at the southwestern margin of the Yangtze Block, represents a geological unit characterized by relatively high-grade metamorphism in the region. This paper investigates the garnet-biotite schist from the Laochanghe Formation of the Dahongshan Group, employing an integrated approach that includes petrological analysis, phase equilibrium modeling, and zircon U–Pb dating. The schist is mainly composed of garnet, biotite, plagioclase, quartz, rutile, and ilmenite. Phase equilibrium modeling revealed the peak metamorphic conditions of 8–9 kbar and 635–675 °C. By further integrating the prograde metamorphic profile of garnet and geothermobarometric results, a clockwise <i>P–T</i> metamorphic evolution path is constructed, which includes an increase in temperature and pressure during the prograde stage. LA–ICP–MS zircon U–Pb dating and zircon Ti thermometry constrains the post-peak metamorphic age of 831.2 ± 7.2 Ma. Integrated with previously reported results, it is revealed that the southwestern margin of the Yangtze Block experienced a large-scale regional metamorphism during the Neoproterozoic (890–750 Ma), which is related to the collisional orogenic process. This may be associated with the late-stage assembly of the Rodinia supercontinent or with local compression and subduction processes during the breakup of the Rodinia supercontinent.</p></div>","PeriodicalId":7151,"journal":{"name":"Acta Geochimica","volume":"43 4","pages":"707 - 718"},"PeriodicalIF":1.4,"publicationDate":"2024-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141012384","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-05-04DOI: 10.1007/s11631-024-00698-y
Gehad M. Saleh, Farrage M. Khaleal, Mohammed Z. El-Bialy, Mohamed S. Kamar, Mokhles K. Azer, Mohamed M. Omar, Mohamed N. El Dawy, Ahmed Abdelaal, El Saeed R. Lasheen
Beryl is the commercial source of beryllium and several varieties of it are valued as a gemstone. To contribute to understanding the mechanism of beryl formation, we carried out detailed geological, petrographical, and geochemical investigations on beryl mineralization occurrences in the Zabara-Wadi El Gemal (Z-WG) region. This region is an NW–SE trending tract that includes six beryl-hosting areas. The green gem variety of beryl (emerald) is restricted to phlogopite schist, pegmatite, and quartz veins. Prismatic hexagonal emerald crystals are well-developed in phlogopite schist and pegmatite. The gem variety emerald examined is sodic and Cr-dominant. It contains high concentrations of chromophore transition elements ordering Cr (up to 1511 ppm) > V (up to 242 ppm) > Sc (up to 245 ppm), giving rise to its vivid green color, reflecting mafic–ultramafic source contribution. Among the investigated emeralds, the Sikait area contains the highest BeO (av. 10.76wt.%) concentration. The compositional variability of emeralds is most likely attributed to the contribution from the host rocks. This is revealed by the examined emerald mineralization, for instance; the Abu Rusheid area (one of the best areas exposing rare metal-bearing granitoids) possesses the highest average of trace and REEs concentrations. In contrast, Um Kabu emerald has the highest contents of Co (av. 20 ppm), Ni (av. 299 ppm), MgO (av. 8.2wt.%), Fe2O3 (av. 3.12wt.%), and CaO (avg. 3.4wt.%) relative to other areas, which may be linked to contribution of ultramafic rocks exposed there. The proposed mechanism we suggest for emerald genesis is metasomatic interaction between felsic (intrusions, that are enriched with K, Na, Be, Li, and B, with mafic–ultramafic rocks that are enriched in Cr, V, Mg, Fe, and Ca. This interaction is marked by the formation of phlogopite schist, the growth of emerald crystals, and desilicated pegmatite.
绿柱石是铍的商业来源,有多个品种的绿柱石被珍视为宝石。为了帮助了解绿柱石的形成机制,我们对 Zabara-Wadi El Gemal(Z-WG)地区的绿柱石矿化现象进行了详细的地质、岩相和地球化学调查。该地区呈西北-东南走向,包括六个绿柱石矿床区。绿柱石的绿色宝石品种(祖母绿)仅限于辉绿岩片岩、伟晶岩和石英脉。棱柱状六角形祖母绿晶体在辉绿岩片岩和伟晶岩中非常发达。经检测,宝石品种祖母绿呈钠态且以铬为主。它含有高浓度的发色过渡元素,包括铬(高达百万分之 1511)、钒(高达百万分之 242)和钪(高达百万分之 245),从而形成了鲜艳的绿色,反映了黑云母-超黑云母来源的贡献。在所调查的祖母绿中,Sikait 地区的氧化铍(平均 10.76wt.%)含量最高。祖母绿成分的多变性很可能是由寄主岩造成的。例如,Abu Rusheid 地区(揭露含稀有金属花岗岩的最佳地区之一)的微量元素和稀土元素平均浓度最高。相比之下,Um Kabu 绿宝石的钴(平均百万分之 20)、镍(平均百万分之 299)、氧化镁(平均 8.2wt.%)、氧化铁(平均 3.12wt.%)和氧化钙(平均 3.4wt.%)的含量相对其他地区最高,这可能与该地区出露的超基性岩有关。我们提出的祖母绿成因机制是富含 K、Na、Be、Li 和 B 的长英质(侵入体)与富含 Cr、V、Mg、Fe 和 Ca 的黑云母-超黑云母岩之间的成岩作用。这种相互作用的标志是辉绿岩片岩的形成、绿宝石晶体的生长以及脱硅伟晶岩。
{"title":"Origin and geochemical characteristics of beryllium mineralization in the Zabara-Wadi El Gemal region, South Eastern Desert, Egypt","authors":"Gehad M. Saleh, Farrage M. Khaleal, Mohammed Z. El-Bialy, Mohamed S. Kamar, Mokhles K. Azer, Mohamed M. Omar, Mohamed N. El Dawy, Ahmed Abdelaal, El Saeed R. Lasheen","doi":"10.1007/s11631-024-00698-y","DOIUrl":"10.1007/s11631-024-00698-y","url":null,"abstract":"<div><p>Beryl is the commercial source of beryllium and several varieties of it are valued as a gemstone. To contribute to understanding the mechanism of beryl formation, we carried out detailed geological, petrographical, and geochemical investigations on beryl mineralization occurrences in the Zabara-Wadi El Gemal (Z-WG) region. This region is an NW–SE trending tract that includes six beryl-hosting areas. The green gem variety of beryl (emerald) is restricted to phlogopite schist, pegmatite, and quartz veins. Prismatic hexagonal emerald crystals are well-developed in phlogopite schist and pegmatite. The gem variety emerald examined is sodic and Cr-dominant. It contains high concentrations of chromophore transition elements ordering Cr (up to 1511 ppm) > V (up to 242 ppm) > Sc (up to 245 ppm), giving rise to its vivid green color, reflecting mafic–ultramafic source contribution. Among the investigated emeralds, the Sikait area contains the highest BeO (av. 10.76wt.%) concentration. The compositional variability of emeralds is most likely attributed to the contribution from the host rocks. This is revealed by the examined emerald mineralization, for instance; the Abu Rusheid area (one of the best areas exposing rare metal-bearing granitoids) possesses the highest average of trace and REEs concentrations. In contrast, Um Kabu emerald has the highest contents of Co (av. 20 ppm), Ni (av. 299 ppm), MgO (av. 8.2wt.%), Fe<sub>2</sub>O<sub>3</sub> (av. 3.12wt.%), and CaO (avg. 3.4wt.%) relative to other areas, which may be linked to contribution of ultramafic rocks exposed there. The proposed mechanism we suggest for emerald genesis is metasomatic interaction between felsic (intrusions, that are enriched with K, Na, Be, Li, and B, with mafic–ultramafic rocks that are enriched in Cr, V, Mg, Fe, and Ca. This interaction is marked by the formation of phlogopite schist, the growth of emerald crystals, and desilicated pegmatite.</p></div>","PeriodicalId":7151,"journal":{"name":"Acta Geochimica","volume":"43 6","pages":"1105 - 1122"},"PeriodicalIF":1.4,"publicationDate":"2024-05-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141014214","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}