{"title":"钒镍卟啉在伍德福德页岩中的分布及不同四吡咯构型对金属的选择性螯合作用","authors":"Derek R. Parks, Xiao-Lei Liu","doi":"10.1016/j.orggeochem.2023.104693","DOIUrl":null,"url":null,"abstract":"<div><p>Abundant vanadyl (VO) and nickel (Ni) porphyrins were detected in the Late Devonian–Early Mississippian Woodford formation shales using a recently developed reverse-phase liquid chromatography quadrupole time-of-flight mass spectrometry with electrospray ionization (RPLC-ESI-qTOF-MS) method. This Woodford shale sequence is characterized by the presence of sustained photic zone euxinia (PZE), as indicated by the occurrence of green sulfur bacteria-produced isorenieratane. The distribution of VO- and Ni-porphyrins, expressed as the VO/(VO + Ni) ratio, reflects a generally reducing/sulfidic condition throughout most of the Woodford deposition. However, in the later Upper Woodford, there is a significant drop in the VO/(VO + Ni) ratio, marking the collapse of anoxia/euxinia due to gradual oxygenation. The depth profiles of VO- and Ni-porphyrin concentrations exhibit a remarkable increase during the peak of PZE in the Middle Woodford, implying that Ni-porphyrin is not completely limited by sulfide. All three categories of porphyrin structures, namely bicycloalkanoporphyrin (BiCAP), deoxophylloerythroethioporphyrin (DPEP), and etioporphyrin (Etio), occurred in VO- and Ni-porphyrins. VO<sup>2+</sup> exhibits a preferential chelation to BiCAP over the other two types of porphyrins. In contrast, Ni-porphyrins are predominantly composed of Etio structures. Due to such selective binding of metal species to specific porphyrin structures, the relative abundance of VO- and Ni-porphyrins (VO/Ni) exhibits a strong positive correlation (<em>R</em><sup>2</sup> > 0.83) with the ratio of BiCAP to Etio (BiCAP/Etio). These findings suggest that the distribution of VO- and Ni-porphyrins in sediments is not solely controlled by the availability of metal ions. When both VO<sup>2+</sup> and Ni<sup>2+</sup> are not limited, the molecular configurations of porphyrins determine the relative abundance of VO- and Ni-porphyrins. Further investigations into the influence of biological and diagenetic processes on the production of BiCAP and Etio are crucial and warrant future research endeavors.</p></div>","PeriodicalId":400,"journal":{"name":"Organic Geochemistry","volume":"186 ","pages":"Article 104693"},"PeriodicalIF":2.6000,"publicationDate":"2023-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Distributions of vanadyl and nickel porphyrins in the Woodford Shale and selective chelation of metal species by different tetrapyrrole configurations\",\"authors\":\"Derek R. Parks, Xiao-Lei Liu\",\"doi\":\"10.1016/j.orggeochem.2023.104693\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Abundant vanadyl (VO) and nickel (Ni) porphyrins were detected in the Late Devonian–Early Mississippian Woodford formation shales using a recently developed reverse-phase liquid chromatography quadrupole time-of-flight mass spectrometry with electrospray ionization (RPLC-ESI-qTOF-MS) method. This Woodford shale sequence is characterized by the presence of sustained photic zone euxinia (PZE), as indicated by the occurrence of green sulfur bacteria-produced isorenieratane. The distribution of VO- and Ni-porphyrins, expressed as the VO/(VO + Ni) ratio, reflects a generally reducing/sulfidic condition throughout most of the Woodford deposition. However, in the later Upper Woodford, there is a significant drop in the VO/(VO + Ni) ratio, marking the collapse of anoxia/euxinia due to gradual oxygenation. The depth profiles of VO- and Ni-porphyrin concentrations exhibit a remarkable increase during the peak of PZE in the Middle Woodford, implying that Ni-porphyrin is not completely limited by sulfide. All three categories of porphyrin structures, namely bicycloalkanoporphyrin (BiCAP), deoxophylloerythroethioporphyrin (DPEP), and etioporphyrin (Etio), occurred in VO- and Ni-porphyrins. VO<sup>2+</sup> exhibits a preferential chelation to BiCAP over the other two types of porphyrins. In contrast, Ni-porphyrins are predominantly composed of Etio structures. Due to such selective binding of metal species to specific porphyrin structures, the relative abundance of VO- and Ni-porphyrins (VO/Ni) exhibits a strong positive correlation (<em>R</em><sup>2</sup> > 0.83) with the ratio of BiCAP to Etio (BiCAP/Etio). These findings suggest that the distribution of VO- and Ni-porphyrins in sediments is not solely controlled by the availability of metal ions. When both VO<sup>2+</sup> and Ni<sup>2+</sup> are not limited, the molecular configurations of porphyrins determine the relative abundance of VO- and Ni-porphyrins. Further investigations into the influence of biological and diagenetic processes on the production of BiCAP and Etio are crucial and warrant future research endeavors.</p></div>\",\"PeriodicalId\":400,\"journal\":{\"name\":\"Organic Geochemistry\",\"volume\":\"186 \",\"pages\":\"Article 104693\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2023-11-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic Geochemistry\",\"FirstCategoryId\":\"89\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0146638023001390\",\"RegionNum\":3,\"RegionCategory\":\"地球科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"GEOCHEMISTRY & GEOPHYSICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic Geochemistry","FirstCategoryId":"89","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0146638023001390","RegionNum":3,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GEOCHEMISTRY & GEOPHYSICS","Score":null,"Total":0}
Distributions of vanadyl and nickel porphyrins in the Woodford Shale and selective chelation of metal species by different tetrapyrrole configurations
Abundant vanadyl (VO) and nickel (Ni) porphyrins were detected in the Late Devonian–Early Mississippian Woodford formation shales using a recently developed reverse-phase liquid chromatography quadrupole time-of-flight mass spectrometry with electrospray ionization (RPLC-ESI-qTOF-MS) method. This Woodford shale sequence is characterized by the presence of sustained photic zone euxinia (PZE), as indicated by the occurrence of green sulfur bacteria-produced isorenieratane. The distribution of VO- and Ni-porphyrins, expressed as the VO/(VO + Ni) ratio, reflects a generally reducing/sulfidic condition throughout most of the Woodford deposition. However, in the later Upper Woodford, there is a significant drop in the VO/(VO + Ni) ratio, marking the collapse of anoxia/euxinia due to gradual oxygenation. The depth profiles of VO- and Ni-porphyrin concentrations exhibit a remarkable increase during the peak of PZE in the Middle Woodford, implying that Ni-porphyrin is not completely limited by sulfide. All three categories of porphyrin structures, namely bicycloalkanoporphyrin (BiCAP), deoxophylloerythroethioporphyrin (DPEP), and etioporphyrin (Etio), occurred in VO- and Ni-porphyrins. VO2+ exhibits a preferential chelation to BiCAP over the other two types of porphyrins. In contrast, Ni-porphyrins are predominantly composed of Etio structures. Due to such selective binding of metal species to specific porphyrin structures, the relative abundance of VO- and Ni-porphyrins (VO/Ni) exhibits a strong positive correlation (R2 > 0.83) with the ratio of BiCAP to Etio (BiCAP/Etio). These findings suggest that the distribution of VO- and Ni-porphyrins in sediments is not solely controlled by the availability of metal ions. When both VO2+ and Ni2+ are not limited, the molecular configurations of porphyrins determine the relative abundance of VO- and Ni-porphyrins. Further investigations into the influence of biological and diagenetic processes on the production of BiCAP and Etio are crucial and warrant future research endeavors.
期刊介绍:
Organic Geochemistry serves as the only dedicated medium for the publication of peer-reviewed research on all phases of geochemistry in which organic compounds play a major role. The Editors welcome contributions covering a wide spectrum of subjects in the geosciences broadly based on organic chemistry (including molecular and isotopic geochemistry), and involving geology, biogeochemistry, environmental geochemistry, chemical oceanography and hydrology.
The scope of the journal includes research involving petroleum (including natural gas), coal, organic matter in the aqueous environment and recent sediments, organic-rich rocks and soils and the role of organics in the geochemical cycling of the elements.
Sedimentological, paleontological and organic petrographic studies will also be considered for publication, provided that they are geochemically oriented. Papers cover the full range of research activities in organic geochemistry, and include comprehensive review articles, technical communications, discussion/reply correspondence and short technical notes. Peer-reviews organised through three Chief Editors and a staff of Associate Editors, are conducted by well known, respected scientists from academia, government and industry. The journal also publishes reviews of books, announcements of important conferences and meetings and other matters of direct interest to the organic geochemical community.