{"title":"早古生代海水化学成分的特殊性(鄂尔多斯奥陶系盐盆地岩盐岩流体包裹体研究)","authors":"A. Galamay, F. Meng, D. Sydor, Yongsheng Zhang","doi":"10.15407/ggcm2019.04.078","DOIUrl":null,"url":null,"abstract":"The fluid inclusions in the marine Middle Ordovician halite of the Majiagou Salt Formation of the Ordos Basin (China) have been investigated. In addition to the primary inclusions the secondary ones of several generations were also detected. The fluid inclusions brine chemistry of halite was studied using an ultramicrochemical (UMCA) method, and the homogenization temperature of fluid inclusions was determined in a special thermal chamber designed by V. A. Kalyuzhny At the post-sedimentation stage, the studied salt strata were exposed to high temperature (58–72 °C) and high (up to several tens of MPa) pressure. Although there are opinions of the inability of primary inclusions in such halite to determine the physical and chemical conditions of sedimentation, however, the informative value of primary inclusions in halite of the Majiagou Formation has remained. The preservation of the integrity (and thus the informative value) of primary inclusions in halite is evidenced by the same chemistry of their brines, which differs from that of secondary inclusions The sedimentation brines of the basin were concentrated to the middle of halite stage and points to the Na-K-Mg-Ca-Cl seawater. The physical and chemical conditions of evaporites formation are not known enough. Currently, the results of the brine chemistry of primary fluid inclusions in marine halite are the best indicators of seawater composition in the Phanerozoic. It is established that the magnesium content in the brines of the Lower Paleozoic basins is lower comparing to modern seawater of the corresponding concentration, and the potassium ion concentration is higher. The chemical composition of the concentrated seawater from which the halite was crystallized in the Ordovician salt basin of Ordos, with the exception of the calcium ion content, is similar to the seawater chemistry of the Cambrian and Silurian basins, which indicates the relative constancy of Early Paleozoic seawater chemistry. Age-related changes in the chemical composition of seawater are always consistent with many quantitatively or qualitatively characterized processes of the Earth’s crust evolution. So we believe that the causes that led to more than twice the potassium content of Riphean-Devonian clays, unlike the younger ones, it were also the reason for the increase in potassium content in the Lower Paleozoic marine brines. The studies conducted also clarify the limits of oscillation of calcium ion content, which determines the type of seawater. Its content in the sedimentary brines of the Ordos basin of the Middle Ordovician reaches 66 g/l at the middle of halite stage. Therefore, at the beginning of the stage of halite precipitation, its content should be approximately 20 g/l (considering its theoretical content of 10 g/l with the modern composition of the atmosphere). Apparently, the cause of the abnormally high calcium content in the early Paleozoic Ocean was the direct flow of it with hydrothermal solutions into the ocean during the activation of global tectonics of the Earth and the increase of solubility of carbonates of continents and ocean floor due to high carbon dioxide atmospheric content.","PeriodicalId":176324,"journal":{"name":"Geology and Geochemistry of Combustible Minerals","volume":"57 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Peculiarities of chemical composition of Early Paleozoic seawater (study of fluid inclusions in halite of Ordovician Ordos salt basin, China)\",\"authors\":\"A. Galamay, F. Meng, D. Sydor, Yongsheng Zhang\",\"doi\":\"10.15407/ggcm2019.04.078\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The fluid inclusions in the marine Middle Ordovician halite of the Majiagou Salt Formation of the Ordos Basin (China) have been investigated. In addition to the primary inclusions the secondary ones of several generations were also detected. The fluid inclusions brine chemistry of halite was studied using an ultramicrochemical (UMCA) method, and the homogenization temperature of fluid inclusions was determined in a special thermal chamber designed by V. A. Kalyuzhny At the post-sedimentation stage, the studied salt strata were exposed to high temperature (58–72 °C) and high (up to several tens of MPa) pressure. Although there are opinions of the inability of primary inclusions in such halite to determine the physical and chemical conditions of sedimentation, however, the informative value of primary inclusions in halite of the Majiagou Formation has remained. The preservation of the integrity (and thus the informative value) of primary inclusions in halite is evidenced by the same chemistry of their brines, which differs from that of secondary inclusions The sedimentation brines of the basin were concentrated to the middle of halite stage and points to the Na-K-Mg-Ca-Cl seawater. The physical and chemical conditions of evaporites formation are not known enough. Currently, the results of the brine chemistry of primary fluid inclusions in marine halite are the best indicators of seawater composition in the Phanerozoic. It is established that the magnesium content in the brines of the Lower Paleozoic basins is lower comparing to modern seawater of the corresponding concentration, and the potassium ion concentration is higher. The chemical composition of the concentrated seawater from which the halite was crystallized in the Ordovician salt basin of Ordos, with the exception of the calcium ion content, is similar to the seawater chemistry of the Cambrian and Silurian basins, which indicates the relative constancy of Early Paleozoic seawater chemistry. Age-related changes in the chemical composition of seawater are always consistent with many quantitatively or qualitatively characterized processes of the Earth’s crust evolution. So we believe that the causes that led to more than twice the potassium content of Riphean-Devonian clays, unlike the younger ones, it were also the reason for the increase in potassium content in the Lower Paleozoic marine brines. The studies conducted also clarify the limits of oscillation of calcium ion content, which determines the type of seawater. Its content in the sedimentary brines of the Ordos basin of the Middle Ordovician reaches 66 g/l at the middle of halite stage. Therefore, at the beginning of the stage of halite precipitation, its content should be approximately 20 g/l (considering its theoretical content of 10 g/l with the modern composition of the atmosphere). Apparently, the cause of the abnormally high calcium content in the early Paleozoic Ocean was the direct flow of it with hydrothermal solutions into the ocean during the activation of global tectonics of the Earth and the increase of solubility of carbonates of continents and ocean floor due to high carbon dioxide atmospheric content.\",\"PeriodicalId\":176324,\"journal\":{\"name\":\"Geology and Geochemistry of Combustible Minerals\",\"volume\":\"57 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-12-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Geology and Geochemistry of Combustible Minerals\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.15407/ggcm2019.04.078\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Geology and Geochemistry of Combustible Minerals","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15407/ggcm2019.04.078","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
对鄂尔多斯盆地马家沟盐组海相中奥陶统岩盐岩流体包裹体进行了研究。除了原生包裹体外,还发现了几代的次生包裹体。采用超显微化学(UMCA)方法研究了岩盐流体包裹体的卤水化学,并在V. a . Kalyuzhny设计的特殊热室中测定了流体包裹体的均一温度。沉积后阶段,研究的盐层暴露于高温(58 ~ 72℃)和高压(高达几十MPa)下。虽然有观点认为马家沟组岩盐岩原生包裹体不能确定沉积的物理和化学条件,但马家沟组岩盐岩原生包裹体的信息价值仍然存在。原生包裹体的卤水化学性质与次生包裹体的相同,证明了原生包裹体的完整性(因而具有信息价值)。盆地沉积卤水集中于岩盐期中期,指向Na-K-Mg-Ca-Cl海水。蒸发岩形成的物理和化学条件尚不清楚。目前,海相岩盐原生流体包裹体的卤水化学结果是反映显生界海水成分的最佳指标。确定下古生界盆地卤水中镁元素含量低于现代相应浓度的海水,而钾离子浓度较高。鄂尔多斯奥陶系盐盆地盐岩结晶的浓缩海水化学成分除钙离子含量外,与寒武系和志留系的海水化学成分相似,表明早古生代的海水化学成分具有相对的稳定性。与年龄相关的海水化学成分的变化总是与地壳演化的许多定量或定性特征过程相一致。因此,我们认为,与更年轻的粘土不同,导致里芬-泥盆纪粘土钾含量增加两倍以上的原因,也是下古生代海洋盐水钾含量增加的原因。所进行的研究还阐明了钙离子含量的振荡限度,钙离子含量决定了海水的类型。中奥陶统鄂尔多斯盆地沉积盐水中,其含量在岩盐期中期达到66 g/l。因此,在岩盐沉淀阶段开始时,其含量应约为20 g/l(考虑到其理论含量为10 g/l,以现代大气组成)。显然,早古生代海洋钙含量异常高的原因是全球构造活动期间,钙随热液直接流入海洋,以及大气中二氧化碳含量高导致大陆和洋底碳酸盐溶解度增加。
Peculiarities of chemical composition of Early Paleozoic seawater (study of fluid inclusions in halite of Ordovician Ordos salt basin, China)
The fluid inclusions in the marine Middle Ordovician halite of the Majiagou Salt Formation of the Ordos Basin (China) have been investigated. In addition to the primary inclusions the secondary ones of several generations were also detected. The fluid inclusions brine chemistry of halite was studied using an ultramicrochemical (UMCA) method, and the homogenization temperature of fluid inclusions was determined in a special thermal chamber designed by V. A. Kalyuzhny At the post-sedimentation stage, the studied salt strata were exposed to high temperature (58–72 °C) and high (up to several tens of MPa) pressure. Although there are opinions of the inability of primary inclusions in such halite to determine the physical and chemical conditions of sedimentation, however, the informative value of primary inclusions in halite of the Majiagou Formation has remained. The preservation of the integrity (and thus the informative value) of primary inclusions in halite is evidenced by the same chemistry of their brines, which differs from that of secondary inclusions The sedimentation brines of the basin were concentrated to the middle of halite stage and points to the Na-K-Mg-Ca-Cl seawater. The physical and chemical conditions of evaporites formation are not known enough. Currently, the results of the brine chemistry of primary fluid inclusions in marine halite are the best indicators of seawater composition in the Phanerozoic. It is established that the magnesium content in the brines of the Lower Paleozoic basins is lower comparing to modern seawater of the corresponding concentration, and the potassium ion concentration is higher. The chemical composition of the concentrated seawater from which the halite was crystallized in the Ordovician salt basin of Ordos, with the exception of the calcium ion content, is similar to the seawater chemistry of the Cambrian and Silurian basins, which indicates the relative constancy of Early Paleozoic seawater chemistry. Age-related changes in the chemical composition of seawater are always consistent with many quantitatively or qualitatively characterized processes of the Earth’s crust evolution. So we believe that the causes that led to more than twice the potassium content of Riphean-Devonian clays, unlike the younger ones, it were also the reason for the increase in potassium content in the Lower Paleozoic marine brines. The studies conducted also clarify the limits of oscillation of calcium ion content, which determines the type of seawater. Its content in the sedimentary brines of the Ordos basin of the Middle Ordovician reaches 66 g/l at the middle of halite stage. Therefore, at the beginning of the stage of halite precipitation, its content should be approximately 20 g/l (considering its theoretical content of 10 g/l with the modern composition of the atmosphere). Apparently, the cause of the abnormally high calcium content in the early Paleozoic Ocean was the direct flow of it with hydrothermal solutions into the ocean during the activation of global tectonics of the Earth and the increase of solubility of carbonates of continents and ocean floor due to high carbon dioxide atmospheric content.