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Lianchang Zhang - One of the best experts on this subject based on the ideXlab platform.

  • depositional environment of the paleoproterozoic yuanjiacun banded iron formation in shanxi province china
    Economic Geology, 2015
    Co-Authors: Changle Wang, Kurt O. Konhauser, Lianchang Zhang
    Abstract:

    The Paleoproterozoic (~2.38–2.21 Ga) Yuanjiacun banded iron formation (BIF), located in Shanxi Province, is a Superior-type BIF in the North China craton. This BIF is within a Metasedimentary Rock succession of the Yuanjiacun Formation, in the lower Luliang Group, which has undergone lower greenschist-facies metamor phism. Iron oxide (magnetite and hematite), carbonate, and silicate facies are all present within the iron-rich layers. The eastward transition from carbonate- into oxide-facies iron formations is accompanied by a change in mineralogical composition from siderite in the west through magnetite-ankerite and magnetite-stilpnomelane assemblages in the transition zone to magnetite and then hematite in the east. These distinct lateral facies are also observed vertically within the BIF, i.e., the iron mineral assemblage changes upsection from sider ite through magnetite into hematite-rich iron formation. The oxide-facies BIF formed near shore, whereas carbonate (siderite)- and silicate-facies assemblages formed in deeper waters. Based on detailed analyses of these variations on a basinal scale, the BIF precipitated during a transgressive event within an environment that ranged from deep waters below storm wave base to relatively shallow waters. The BIF samples display distinctively seawater-like REEs + Y profiles that are characterized by positive La and Y anomalies and HREEs enrichment relative to LREEs in Post-Archean Australian shale-normalized diagrams. Consistently positive Eu anomalies are also observed, which are typical of reduced, high-temperature hydrothermal fluids. In addition, slightly negative to positive Ce anomalies, and a large range in ratios of light to heavy REEs, are present in the oxide-facies BIF. These characteristics, in combination with consistently positive δ 56Fe values, suggest that deposition of the BIF took place along the chemocline where upwelling of deep, anoxic, iron- and silicarich hydrothermal fluids mixed with shallower and slightly oxygenated seawater. The ankerite displays highly depleted δ13C values and the carbonate-rich BIF has a high content of organic carbon, suggesting dissimilatory Fe(III) reduction of a ferric oxyhydroxide precursor during burial of biomass deposited from the water column; that same biomass was likely tied to the original oxidation of dissolved Fe(II). The fact that the more ferric BIF facies formed in shallower waters suggests that river-sourced nutrients would have been minimal, thus limiting primary productivity in the shallow waters and minimizing the organic carbon source necessary for reducing the hematite via dissimilatory Fe(III) reduction. By contrast, in deeper waters more proximal to the hydrothermal vents, nutrients were abundant, and high biomass productivity was coupled to increased carbon burial, leading to the deposition of iron-rich carbonates. The deposition of the Yuanjiacun BIF during the onset of the Great Oxidation Event (GOE; ca. 2.4–2.2 Ga) confirms that deep marine waters during this time period were still episodically ferruginous, but that shallow waters were sufficiently oxygenated that Fe(II) oxidation no longer needed to be tied directly to proximal cyanobacterial activity.

  • depositional environment of the paleoproterozoic yuanjiacun banded iron formation in shanxi province china
    Economic Geology, 2015
    Co-Authors: Changle Wang, Kurt O. Konhauser, Lianchang Zhang
    Abstract:

    The Paleoproterozoic (~2.38–2.21 Ga) Yuanjiacun banded iron formation (BIF), located in Shanxi Province, is a Superior-type BIF in the North China craton. This BIF is within a Metasedimentary Rock succession of the Yuanjiacun Formation, in the lower Luliang Group, which has undergone lower greenschist-facies metamor phism. Iron oxide (magnetite and hematite), carbonate, and silicate facies are all present within the iron-rich layers. The eastward transition from carbonate- into oxide-facies iron formations is accompanied by a change in mineralogical composition from siderite in the west through magnetite-ankerite and magnetite-stilpnomelane assemblages in the transition zone to magnetite and then hematite in the east. These distinct lateral facies are also observed vertically within the BIF, i.e., the iron mineral assemblage changes upsection from sider ite through magnetite into hematite-rich iron formation. The oxide-facies BIF formed near shore, whereas carbonate (siderite)- and silicate-facies assemblages formed in deeper waters. Based on detailed analyses of these variations on a basinal scale, the BIF precipitated during a transgressive event within an environment that ranged from deep waters below storm wave base to relatively shallow waters. The BIF samples display distinctively seawater-like REEs + Y profiles that are characterized by positive La and Y anomalies and HREEs enrichment relative to LREEs in Post-Archean Australian shale-normalized diagrams. Consistently positive Eu anomalies are also observed, which are typical of reduced, high-temperature hydrothermal fluids. In addition, slightly negative to positive Ce anomalies, and a large range in ratios of light to heavy REEs, are present in the oxide-facies BIF. These characteristics, in combination with consistently positive δ 56Fe values, suggest that deposition of the BIF took place along the chemocline where upwelling of deep, anoxic, iron- and silicarich hydrothermal fluids mixed with shallower and slightly oxygenated seawater. The ankerite displays highly depleted δ13C values and the carbonate-rich BIF has a high content of organic carbon, suggesting dissimilatory Fe(III) reduction of a ferric oxyhydroxide precursor during burial of biomass deposited from the water column; that same biomass was likely tied to the original oxidation of dissolved Fe(II). The fact that the more ferric BIF facies formed in shallower waters suggests that river-sourced nutrients would have been minimal, thus limiting primary productivity in the shallow waters and minimizing the organic carbon source necessary for reducing the hematite via dissimilatory Fe(III) reduction. By contrast, in deeper waters more proximal to the hydrothermal vents, nutrients were abundant, and high biomass productivity was coupled to increased carbon burial, leading to the deposition of iron-rich carbonates. The deposition of the Yuanjiacun BIF during the onset of the Great Oxidation Event (GOE; ca. 2.4–2.2 Ga) confirms that deep marine waters during this time period were still episodically ferruginous, but that shallow waters were sufficiently oxygenated that Fe(II) oxidation no longer needed to be tied directly to proximal cyanobacterial activity.

Kurt O. Konhauser - One of the best experts on this subject based on the ideXlab platform.

  • depositional environment of the paleoproterozoic yuanjiacun banded iron formation in shanxi province china
    Economic Geology, 2015
    Co-Authors: Changle Wang, Kurt O. Konhauser, Lianchang Zhang
    Abstract:

    The Paleoproterozoic (~2.38–2.21 Ga) Yuanjiacun banded iron formation (BIF), located in Shanxi Province, is a Superior-type BIF in the North China craton. This BIF is within a Metasedimentary Rock succession of the Yuanjiacun Formation, in the lower Luliang Group, which has undergone lower greenschist-facies metamor phism. Iron oxide (magnetite and hematite), carbonate, and silicate facies are all present within the iron-rich layers. The eastward transition from carbonate- into oxide-facies iron formations is accompanied by a change in mineralogical composition from siderite in the west through magnetite-ankerite and magnetite-stilpnomelane assemblages in the transition zone to magnetite and then hematite in the east. These distinct lateral facies are also observed vertically within the BIF, i.e., the iron mineral assemblage changes upsection from sider ite through magnetite into hematite-rich iron formation. The oxide-facies BIF formed near shore, whereas carbonate (siderite)- and silicate-facies assemblages formed in deeper waters. Based on detailed analyses of these variations on a basinal scale, the BIF precipitated during a transgressive event within an environment that ranged from deep waters below storm wave base to relatively shallow waters. The BIF samples display distinctively seawater-like REEs + Y profiles that are characterized by positive La and Y anomalies and HREEs enrichment relative to LREEs in Post-Archean Australian shale-normalized diagrams. Consistently positive Eu anomalies are also observed, which are typical of reduced, high-temperature hydrothermal fluids. In addition, slightly negative to positive Ce anomalies, and a large range in ratios of light to heavy REEs, are present in the oxide-facies BIF. These characteristics, in combination with consistently positive δ 56Fe values, suggest that deposition of the BIF took place along the chemocline where upwelling of deep, anoxic, iron- and silicarich hydrothermal fluids mixed with shallower and slightly oxygenated seawater. The ankerite displays highly depleted δ13C values and the carbonate-rich BIF has a high content of organic carbon, suggesting dissimilatory Fe(III) reduction of a ferric oxyhydroxide precursor during burial of biomass deposited from the water column; that same biomass was likely tied to the original oxidation of dissolved Fe(II). The fact that the more ferric BIF facies formed in shallower waters suggests that river-sourced nutrients would have been minimal, thus limiting primary productivity in the shallow waters and minimizing the organic carbon source necessary for reducing the hematite via dissimilatory Fe(III) reduction. By contrast, in deeper waters more proximal to the hydrothermal vents, nutrients were abundant, and high biomass productivity was coupled to increased carbon burial, leading to the deposition of iron-rich carbonates. The deposition of the Yuanjiacun BIF during the onset of the Great Oxidation Event (GOE; ca. 2.4–2.2 Ga) confirms that deep marine waters during this time period were still episodically ferruginous, but that shallow waters were sufficiently oxygenated that Fe(II) oxidation no longer needed to be tied directly to proximal cyanobacterial activity.

  • depositional environment of the paleoproterozoic yuanjiacun banded iron formation in shanxi province china
    Economic Geology, 2015
    Co-Authors: Changle Wang, Kurt O. Konhauser, Lianchang Zhang
    Abstract:

    The Paleoproterozoic (~2.38–2.21 Ga) Yuanjiacun banded iron formation (BIF), located in Shanxi Province, is a Superior-type BIF in the North China craton. This BIF is within a Metasedimentary Rock succession of the Yuanjiacun Formation, in the lower Luliang Group, which has undergone lower greenschist-facies metamor phism. Iron oxide (magnetite and hematite), carbonate, and silicate facies are all present within the iron-rich layers. The eastward transition from carbonate- into oxide-facies iron formations is accompanied by a change in mineralogical composition from siderite in the west through magnetite-ankerite and magnetite-stilpnomelane assemblages in the transition zone to magnetite and then hematite in the east. These distinct lateral facies are also observed vertically within the BIF, i.e., the iron mineral assemblage changes upsection from sider ite through magnetite into hematite-rich iron formation. The oxide-facies BIF formed near shore, whereas carbonate (siderite)- and silicate-facies assemblages formed in deeper waters. Based on detailed analyses of these variations on a basinal scale, the BIF precipitated during a transgressive event within an environment that ranged from deep waters below storm wave base to relatively shallow waters. The BIF samples display distinctively seawater-like REEs + Y profiles that are characterized by positive La and Y anomalies and HREEs enrichment relative to LREEs in Post-Archean Australian shale-normalized diagrams. Consistently positive Eu anomalies are also observed, which are typical of reduced, high-temperature hydrothermal fluids. In addition, slightly negative to positive Ce anomalies, and a large range in ratios of light to heavy REEs, are present in the oxide-facies BIF. These characteristics, in combination with consistently positive δ 56Fe values, suggest that deposition of the BIF took place along the chemocline where upwelling of deep, anoxic, iron- and silicarich hydrothermal fluids mixed with shallower and slightly oxygenated seawater. The ankerite displays highly depleted δ13C values and the carbonate-rich BIF has a high content of organic carbon, suggesting dissimilatory Fe(III) reduction of a ferric oxyhydroxide precursor during burial of biomass deposited from the water column; that same biomass was likely tied to the original oxidation of dissolved Fe(II). The fact that the more ferric BIF facies formed in shallower waters suggests that river-sourced nutrients would have been minimal, thus limiting primary productivity in the shallow waters and minimizing the organic carbon source necessary for reducing the hematite via dissimilatory Fe(III) reduction. By contrast, in deeper waters more proximal to the hydrothermal vents, nutrients were abundant, and high biomass productivity was coupled to increased carbon burial, leading to the deposition of iron-rich carbonates. The deposition of the Yuanjiacun BIF during the onset of the Great Oxidation Event (GOE; ca. 2.4–2.2 Ga) confirms that deep marine waters during this time period were still episodically ferruginous, but that shallow waters were sufficiently oxygenated that Fe(II) oxidation no longer needed to be tied directly to proximal cyanobacterial activity.

  • ancient graphite in the eoarchean quartz pyroxene Rocks from akilia in southern west greenland ii isotopic and chemical compositions and comparison with paleoproterozoic banded iron formations
    Geochimica et Cosmochimica Acta, 2010
    Co-Authors: Dominic Papineau, Kurt O. Konhauser, Jianhua Wang, Bradley T De Gregorio, Rhonda M Stroud, A Steele, Ernesto Pecoits, Marilyn L Fogel
    Abstract:

    We present detailed petrographic surveys of apatite grains in association with carbonaceous material (CM) in two banded iron formations (BIFs) from the Paleoproterozoic of Uruguay and Michigan for comparison with similar mineral associations in the highly debated Akilia Quartz-pyroxene (Qp) Rock. Petrographic and Raman spectroscopic surveys of these Paleoproterozoic BIFs show that apatite grains typically occur in bands parallel to bedding and are more often associated with CM when concentrations of organic matter are high. Carbonaceous material in the Vichadero BIF from Uruguay is generally wellcrystallized graphite and occurs in concentrations around 0.01 wt% with an average d 13 Cgra value of � 28.6 ± 4.4& (1r). In this BIF, only about 5% of apatite grains are associated with graphite. In comparison, CM in the Bijiki BIF from Michigan is also graphitic, but occurs in concentrations around 2.4 wt% with d 13 Cgra values around � 24.0 ± 0.3& (1r). In the Bijiki BIF, more than 78% of apatite grains are associated with CM. Given the geologic context and high levels of CM in the Bijiki BIF, the significantly higher proportion of apatite grains associated with CM in this Rock is interpreted to represent diagenetically altered biomass and shows that such diagenetic mineral associations can survive metamorphism up to the amphibolite facies. Isotope compositions of CM in muffled acidified whole-Rock powders from the Akilia Qp Rock have average d 13 Cgra values of � 17.5 ± 2.5& (1r), while d 13 Ccarb values in whole-Rock powders average � 4.0 ± 1.0& (1r). Carbon isotope compositions of graphite associated with apatite and other minerals in the Akilia Qp Rock were also measured with the NanoSIMS to have similar ranges of d 13 Cgra values averaging � 13.8 ± 5.6& (1r). The NanoSIMS was also used to semi-quantitatively map the distributions of H, N, O, P, and S in graphite from the Akilia Qp Rock, and relative abundances were found to be similar for graphite associated with apatite or with hornblende, calcite, and sulfides. These analyses revealed generally lower abundances of trace elements in the Akilia graphite compared to graphite associated with apatite from Paleoproterozoic BIFs. Graphite associated with hornblende, calcite, and sulfides in the Akilia Qp Rock was fluid-deposited at high-temperature from carbon-bearing fluids, and since this graphite has similar ranges of d 13 Cgra values and of trace elements compared to graphite associated with apatite, we conclude that the Akilia graphite in different mineral associations formed from the same source(s) of CM. Collectively our results do not exclude a biogenic origin of the carbon in the Akilia graphite, but because some observations can not exclude graphitization of abiogenic carbon from CO2- and CH4-bearing mantle fluids, there remain ambiguities with respect to the exact origin of carbon in this ancient Metasedimentary Rock. Accordingly, there

Changle Wang - One of the best experts on this subject based on the ideXlab platform.

  • depositional environment of the paleoproterozoic yuanjiacun banded iron formation in shanxi province china
    Economic Geology, 2015
    Co-Authors: Changle Wang, Kurt O. Konhauser, Lianchang Zhang
    Abstract:

    The Paleoproterozoic (~2.38–2.21 Ga) Yuanjiacun banded iron formation (BIF), located in Shanxi Province, is a Superior-type BIF in the North China craton. This BIF is within a Metasedimentary Rock succession of the Yuanjiacun Formation, in the lower Luliang Group, which has undergone lower greenschist-facies metamor phism. Iron oxide (magnetite and hematite), carbonate, and silicate facies are all present within the iron-rich layers. The eastward transition from carbonate- into oxide-facies iron formations is accompanied by a change in mineralogical composition from siderite in the west through magnetite-ankerite and magnetite-stilpnomelane assemblages in the transition zone to magnetite and then hematite in the east. These distinct lateral facies are also observed vertically within the BIF, i.e., the iron mineral assemblage changes upsection from sider ite through magnetite into hematite-rich iron formation. The oxide-facies BIF formed near shore, whereas carbonate (siderite)- and silicate-facies assemblages formed in deeper waters. Based on detailed analyses of these variations on a basinal scale, the BIF precipitated during a transgressive event within an environment that ranged from deep waters below storm wave base to relatively shallow waters. The BIF samples display distinctively seawater-like REEs + Y profiles that are characterized by positive La and Y anomalies and HREEs enrichment relative to LREEs in Post-Archean Australian shale-normalized diagrams. Consistently positive Eu anomalies are also observed, which are typical of reduced, high-temperature hydrothermal fluids. In addition, slightly negative to positive Ce anomalies, and a large range in ratios of light to heavy REEs, are present in the oxide-facies BIF. These characteristics, in combination with consistently positive δ 56Fe values, suggest that deposition of the BIF took place along the chemocline where upwelling of deep, anoxic, iron- and silicarich hydrothermal fluids mixed with shallower and slightly oxygenated seawater. The ankerite displays highly depleted δ13C values and the carbonate-rich BIF has a high content of organic carbon, suggesting dissimilatory Fe(III) reduction of a ferric oxyhydroxide precursor during burial of biomass deposited from the water column; that same biomass was likely tied to the original oxidation of dissolved Fe(II). The fact that the more ferric BIF facies formed in shallower waters suggests that river-sourced nutrients would have been minimal, thus limiting primary productivity in the shallow waters and minimizing the organic carbon source necessary for reducing the hematite via dissimilatory Fe(III) reduction. By contrast, in deeper waters more proximal to the hydrothermal vents, nutrients were abundant, and high biomass productivity was coupled to increased carbon burial, leading to the deposition of iron-rich carbonates. The deposition of the Yuanjiacun BIF during the onset of the Great Oxidation Event (GOE; ca. 2.4–2.2 Ga) confirms that deep marine waters during this time period were still episodically ferruginous, but that shallow waters were sufficiently oxygenated that Fe(II) oxidation no longer needed to be tied directly to proximal cyanobacterial activity.

  • depositional environment of the paleoproterozoic yuanjiacun banded iron formation in shanxi province china
    Economic Geology, 2015
    Co-Authors: Changle Wang, Kurt O. Konhauser, Lianchang Zhang
    Abstract:

    The Paleoproterozoic (~2.38–2.21 Ga) Yuanjiacun banded iron formation (BIF), located in Shanxi Province, is a Superior-type BIF in the North China craton. This BIF is within a Metasedimentary Rock succession of the Yuanjiacun Formation, in the lower Luliang Group, which has undergone lower greenschist-facies metamor phism. Iron oxide (magnetite and hematite), carbonate, and silicate facies are all present within the iron-rich layers. The eastward transition from carbonate- into oxide-facies iron formations is accompanied by a change in mineralogical composition from siderite in the west through magnetite-ankerite and magnetite-stilpnomelane assemblages in the transition zone to magnetite and then hematite in the east. These distinct lateral facies are also observed vertically within the BIF, i.e., the iron mineral assemblage changes upsection from sider ite through magnetite into hematite-rich iron formation. The oxide-facies BIF formed near shore, whereas carbonate (siderite)- and silicate-facies assemblages formed in deeper waters. Based on detailed analyses of these variations on a basinal scale, the BIF precipitated during a transgressive event within an environment that ranged from deep waters below storm wave base to relatively shallow waters. The BIF samples display distinctively seawater-like REEs + Y profiles that are characterized by positive La and Y anomalies and HREEs enrichment relative to LREEs in Post-Archean Australian shale-normalized diagrams. Consistently positive Eu anomalies are also observed, which are typical of reduced, high-temperature hydrothermal fluids. In addition, slightly negative to positive Ce anomalies, and a large range in ratios of light to heavy REEs, are present in the oxide-facies BIF. These characteristics, in combination with consistently positive δ 56Fe values, suggest that deposition of the BIF took place along the chemocline where upwelling of deep, anoxic, iron- and silicarich hydrothermal fluids mixed with shallower and slightly oxygenated seawater. The ankerite displays highly depleted δ13C values and the carbonate-rich BIF has a high content of organic carbon, suggesting dissimilatory Fe(III) reduction of a ferric oxyhydroxide precursor during burial of biomass deposited from the water column; that same biomass was likely tied to the original oxidation of dissolved Fe(II). The fact that the more ferric BIF facies formed in shallower waters suggests that river-sourced nutrients would have been minimal, thus limiting primary productivity in the shallow waters and minimizing the organic carbon source necessary for reducing the hematite via dissimilatory Fe(III) reduction. By contrast, in deeper waters more proximal to the hydrothermal vents, nutrients were abundant, and high biomass productivity was coupled to increased carbon burial, leading to the deposition of iron-rich carbonates. The deposition of the Yuanjiacun BIF during the onset of the Great Oxidation Event (GOE; ca. 2.4–2.2 Ga) confirms that deep marine waters during this time period were still episodically ferruginous, but that shallow waters were sufficiently oxygenated that Fe(II) oxidation no longer needed to be tied directly to proximal cyanobacterial activity.

Jingsong Wang - One of the best experts on this subject based on the ideXlab platform.

  • identification of ca 850 ma high temperature strongly peraluminous granitoids in southeastern guizhou province south china a result of early extension along the southern margin of the yangtze block
    Precambrian Research, 2018
    Co-Authors: Jiaxi Zhou, Simon A Wilde, Xuance Wang, Hairui Sun, Jingsong Wang
    Abstract:

    Abstract Strongly peraluminous granites are characterized by high A/CNK values (>1.1) and are important for understanding the regional tectonic regime. Here, we present integrated studies of zircon U–Pb ages, trace elements and Lu–Hf isotopes, whole-Rock major and trace elements, and Nd isotope compositions for the newly discovered Nage granite porphyry in southeastern Guizhou Province. The porphyry has a crystallization age of 852 ± 5 Ma and shows wide ranges in SiO2 (64.5–72.51 wt%) and Al2O3 (13.08–19.34 wt%) contents, with low TiO2 (0.41–0.84 wt%) and P2O5 ( 1.1, and they have similar trace element patterns with depletion in high field strength elements (HFSE, e.g., Nb and Ta) and enrichment in large-ion lithophile elements (LILE, e.g., Rb, Th and U). Initial zircon Hf isotopes of the porphyry vary from eHf(t) = −7.6 to −0.6, whereas whole-Rock Nd isotopes are relatively uniform with eNd(t) = −6.0 to −6.7. They record high zircon saturation temperatures (Tzr) (786–842 °C, mostly >810 °C), but low oxygen fugacity (log fO2 = −16 to −25, corresponding to ΔFMQ −3 to ΔFMQ −7) and emplacement pressure of 1.1), K2O/Na2O (0.7–2.6; average 1.4) and CaO/Na2O (0.2–0.8; mostly >0.5) ratios suggest that clay-poor Metasedimentary Rock were dominant in the source. Combined with the Nd–Hf isotopes, we suggest that the Nage granite porphyry formed by anatexis of an immature arkose and greywacke source, which was a mixture of weathered juvenile igneous materials and minor recycled ancient crustal components. The ca. 850 Ma strongly peraluminous granites, along with coeval extension-related magmatism along the southwestern margin of the Yangtze Block, indicate an extensional environment started as early as ca. 850 Ma.

Xuance Wang - One of the best experts on this subject based on the ideXlab platform.

  • identification of ca 850 ma high temperature strongly peraluminous granitoids in southeastern guizhou province south china a result of early extension along the southern margin of the yangtze block
    Precambrian Research, 2018
    Co-Authors: Jiaxi Zhou, Simon A Wilde, Xuance Wang, Hairui Sun, Jingsong Wang
    Abstract:

    Abstract Strongly peraluminous granites are characterized by high A/CNK values (>1.1) and are important for understanding the regional tectonic regime. Here, we present integrated studies of zircon U–Pb ages, trace elements and Lu–Hf isotopes, whole-Rock major and trace elements, and Nd isotope compositions for the newly discovered Nage granite porphyry in southeastern Guizhou Province. The porphyry has a crystallization age of 852 ± 5 Ma and shows wide ranges in SiO2 (64.5–72.51 wt%) and Al2O3 (13.08–19.34 wt%) contents, with low TiO2 (0.41–0.84 wt%) and P2O5 ( 1.1, and they have similar trace element patterns with depletion in high field strength elements (HFSE, e.g., Nb and Ta) and enrichment in large-ion lithophile elements (LILE, e.g., Rb, Th and U). Initial zircon Hf isotopes of the porphyry vary from eHf(t) = −7.6 to −0.6, whereas whole-Rock Nd isotopes are relatively uniform with eNd(t) = −6.0 to −6.7. They record high zircon saturation temperatures (Tzr) (786–842 °C, mostly >810 °C), but low oxygen fugacity (log fO2 = −16 to −25, corresponding to ΔFMQ −3 to ΔFMQ −7) and emplacement pressure of 1.1), K2O/Na2O (0.7–2.6; average 1.4) and CaO/Na2O (0.2–0.8; mostly >0.5) ratios suggest that clay-poor Metasedimentary Rock were dominant in the source. Combined with the Nd–Hf isotopes, we suggest that the Nage granite porphyry formed by anatexis of an immature arkose and greywacke source, which was a mixture of weathered juvenile igneous materials and minor recycled ancient crustal components. The ca. 850 Ma strongly peraluminous granites, along with coeval extension-related magmatism along the southwestern margin of the Yangtze Block, indicate an extensional environment started as early as ca. 850 Ma.