Studies of the mineralogy and sulfur isotope composition of sediment-hosted hydrothermal sulfide minerals in cores are important for understanding the seafloor mineralization environment and material source and recons...Studies of the mineralogy and sulfur isotope composition of sediment-hosted hydrothermal sulfide minerals in cores are important for understanding the seafloor mineralization environment and material source and reconstructing the hydrothermal history.However,the source of ore-forming materials and the history of hydrothermal activity in the southern Okinawa Trough(SOT)remain unclear.Here,the mineralogy and sulfur isotope characteristics of sulfides from gravity core HOBAB4-S2,collected between the Yonaguni Knoll IV hydrothermal field(HF)and the Tangyin HF,was investigated.Enrichments in Zn(up to 321×10^(-6)),Cu(up to73.7×10^(-6)),and Pb(up to 160×10^(-6))and the presence of pyrite,galena,pyrrhotite and minor sphalerite and chalcopyrite provide evidence for the input of hydrothermal materials into the sediments.The pyrite morphologies include disseminated cubic,pentagonal dodecahedron,and framboidal forms.Except for minor framboidal pyrite,euhedral pyrite from core HOBAB4-S2 is mainly of hydrothermal origin with Co/Ni ratios>1 and S/Fe atomic ratios<2 in the Cu-Zn-Pb-rich layers.The occurrences of hexagonal pyrrhotite,high-Co(up to0.17%)pyrite and high-Fe sphalerite indicate that the hydrothermal precipitates formed at medium-high temperatures and low-sulfur fugacity(f S_(2))environments.The δ^(34) S values of sulfides(0.21‰–3.45‰)with low-f S_(2) mineral assemblages(e.g.,pyrrhotite±high-Fe sphalerite)in the core are significantly lower than those of magmatic rocks and seawater,indicating possible incorporation of previously formed biogenic sulfur in the sediment.Combined with the age model of the core,it is suggested that hydrothermal activity likely began in the Tangyin HF before AD 1445–1483 and that at least three active episodes may have occurred since then.展开更多
The Bipindi iron ore district is located in the central section of the Nyong Complex at the northwestern margin of the Congo Craton in Southwest Cameroon.This iron district contains numerous iron mineralization hosted...The Bipindi iron ore district is located in the central section of the Nyong Complex at the northwestern margin of the Congo Craton in Southwest Cameroon.This iron district contains numerous iron mineralization hosted by the Mewongo,Bibole,Kouambo,and Zambi banded iron formations(BIFs).These BIFs contain magnetite as the main iron ore mineral associated with pyrite,and gangue minerals are quartz with minor chlorite and amphibole.The origin of iron ore from these BIFs was investigated using a combination of in-situ magnetite and whole-rock chemistry.The studied BIF ore samples have a narrow range of TFe between 30.90 wt.%and 43.20 wt.%,indicating a low-grade ore.The geochemical signatures of magnetite such as low contents of base metals(e.g.,Cu,Co,V,and Zn)and low Co/Zn ratios<0.85 indicate a hydrothermal origin.Combined with the geochemical features of these BIFs,e.g.,high Fe/Ti and Fe/Al ratios(mean>600 and>75,respectively),we suggest that magnetite was derived from a mixture of seawater and~0.1%low-temperature hydrothermal fluids in an oxidizing environment.Collectively,low-temperature hydrothermal and later metamorphic fluids were necessary for the transformation of the protolith Nyong Complex BIFs to iron ore.展开更多
Summary of main observation and conclusion An efficient and environmentally benign electrochemical oxidative radical C-H trifluoromethylation of arenes by employing Langlois reagent as the CF3 source was developed in ...Summary of main observation and conclusion An efficient and environmentally benign electrochemical oxidative radical C-H trifluoromethylation of arenes by employing Langlois reagent as the CF3 source was developed in this work.Neither transition metal catalysts nor external chemical oxidants were required in this trifluoromethylation process.The reaction could be conducted in gram scale with high reaction efficiency.展开更多
基金The National Natural Science Foundation of China under contract No.91958213the Strategic Priority Research Program of the Chinese Academy of Sciences under contract No.XDB42020402+3 种基金the National Programma on Global Change and AirSea Interaction under contract No.GASI-GEOGE-02the International Partnership Program of the Chinese Academy of Sciences under contract No.133137KYSB20170003the Special Fund for the Taishan Scholar Program of Shandong Province under contract No.ts201511061the National Key Basic Research Program of China under contract No.2013CB429700。
文摘Studies of the mineralogy and sulfur isotope composition of sediment-hosted hydrothermal sulfide minerals in cores are important for understanding the seafloor mineralization environment and material source and reconstructing the hydrothermal history.However,the source of ore-forming materials and the history of hydrothermal activity in the southern Okinawa Trough(SOT)remain unclear.Here,the mineralogy and sulfur isotope characteristics of sulfides from gravity core HOBAB4-S2,collected between the Yonaguni Knoll IV hydrothermal field(HF)and the Tangyin HF,was investigated.Enrichments in Zn(up to 321×10^(-6)),Cu(up to73.7×10^(-6)),and Pb(up to 160×10^(-6))and the presence of pyrite,galena,pyrrhotite and minor sphalerite and chalcopyrite provide evidence for the input of hydrothermal materials into the sediments.The pyrite morphologies include disseminated cubic,pentagonal dodecahedron,and framboidal forms.Except for minor framboidal pyrite,euhedral pyrite from core HOBAB4-S2 is mainly of hydrothermal origin with Co/Ni ratios>1 and S/Fe atomic ratios<2 in the Cu-Zn-Pb-rich layers.The occurrences of hexagonal pyrrhotite,high-Co(up to0.17%)pyrite and high-Fe sphalerite indicate that the hydrothermal precipitates formed at medium-high temperatures and low-sulfur fugacity(f S_(2))environments.The δ^(34) S values of sulfides(0.21‰–3.45‰)with low-f S_(2) mineral assemblages(e.g.,pyrrhotite±high-Fe sphalerite)in the core are significantly lower than those of magmatic rocks and seawater,indicating possible incorporation of previously formed biogenic sulfur in the sediment.Combined with the age model of the core,it is suggested that hydrothermal activity likely began in the Tangyin HF before AD 1445–1483 and that at least three active episodes may have occurred since then.
基金supported by the Central South University Postdoctoral Research Fund(No.22020084)。
文摘The Bipindi iron ore district is located in the central section of the Nyong Complex at the northwestern margin of the Congo Craton in Southwest Cameroon.This iron district contains numerous iron mineralization hosted by the Mewongo,Bibole,Kouambo,and Zambi banded iron formations(BIFs).These BIFs contain magnetite as the main iron ore mineral associated with pyrite,and gangue minerals are quartz with minor chlorite and amphibole.The origin of iron ore from these BIFs was investigated using a combination of in-situ magnetite and whole-rock chemistry.The studied BIF ore samples have a narrow range of TFe between 30.90 wt.%and 43.20 wt.%,indicating a low-grade ore.The geochemical signatures of magnetite such as low contents of base metals(e.g.,Cu,Co,V,and Zn)and low Co/Zn ratios<0.85 indicate a hydrothermal origin.Combined with the geochemical features of these BIFs,e.g.,high Fe/Ti and Fe/Al ratios(mean>600 and>75,respectively),we suggest that magnetite was derived from a mixture of seawater and~0.1%low-temperature hydrothermal fluids in an oxidizing environment.Collectively,low-temperature hydrothermal and later metamorphic fluids were necessary for the transformation of the protolith Nyong Complex BIFs to iron ore.
基金supported by the National Natural Science Foundation of China (No.21702081)Jiangxi Provincial Education Department Foundation (No.GJJ160325).
文摘Summary of main observation and conclusion An efficient and environmentally benign electrochemical oxidative radical C-H trifluoromethylation of arenes by employing Langlois reagent as the CF3 source was developed in this work.Neither transition metal catalysts nor external chemical oxidants were required in this trifluoromethylation process.The reaction could be conducted in gram scale with high reaction efficiency.
