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Petrogenesis of Cretaceous igneous rocks from the Duolong porphyry Cu–Au deposit, central Tibet: evidence from zircon U–Pb geochronology, petrochemistry and Sr–Nd–Pb–Hf isotope characteristics
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The Duolong porphyry Cu–Au deposit (5.4 Mt at 0.72% Cu, 41 t at 0.23 g/t Au) was recently discovered in the southern Qiangtang terrane, central Tibet. Here, new whole‐rock elemental and Sr–Nd–Pb isotope and zircon Hf isotopic data of syn‐ and post‐ore volcanic rocks and barren and ore‐bearing granodiorite porphyries are presented for a reconstruction of magmas associated with Cu–Au mineralization. LA–ICP–MS zircon U–Pb dating yields mean ages of 117.0 ± 2.0 and 120.9 ± 1.7 Ma for ore‐bearing granodiorite porphyry and 105.2 ± 1.3 Ma for post‐ore basaltic andesite. All the samples show high‐K calc‐alkaline compositions, with enrichment of light rare earth elements (LREE) and large ion lithophile elements (LILE: Cs and Rb) and depletion of high field strength elements (HFSE: Nb and Ti), consistent with the geochemical characteristics of arc‐type magmas. Syn‐ and post‐ore volcanic rocks show initial Sr ratios of 0.7045–0.7055, εNd(t) values of −0.8 to 3.6, (206Pb/204Pb)t ratios of 18.408–18.642, (207Pb/204Pb)t of 15.584–15.672 and positive zircon εHf(t) values of 1.3–10.5, likely suggesting they dominantly were derived from metasomatized mantle wedge and contaminated by southern Qiangtang crust. Compared to mafic volcanic rocks, barren and ore‐bearing granodiorite porphyries have relatively high initial Sr isotopic ratios (0.7054–0.7072), low εNd(t) values (−1.7 to −4.0), similar Pb and enriched zircon Hf isotopic compositions [εHf(t) of 1.5–9.7], possibly suggesting more contribution from southern Qiangtang crust. Duolong volcanic rocks and granodiorite porphyries likely formed in a continental arc setting during northward subduction of the Bangong–Nujiang ocean and evolved at the base of the lower crust by MASH (melting, assimilation, storage and homogenization) processes. Copyright © 2014 John Wiley & Sons, Ltd.
Title: Petrogenesis of Cretaceous igneous rocks from the Duolong porphyry Cu–Au deposit, central Tibet: evidence from zircon U–Pb geochronology, petrochemistry and Sr–Nd–Pb–Hf isotope characteristics
Description:
The Duolong porphyry Cu–Au deposit (5.
4 Mt at 0.
72% Cu, 41 t at 0.
23 g/t Au) was recently discovered in the southern Qiangtang terrane, central Tibet.
Here, new whole‐rock elemental and Sr–Nd–Pb isotope and zircon Hf isotopic data of syn‐ and post‐ore volcanic rocks and barren and ore‐bearing granodiorite porphyries are presented for a reconstruction of magmas associated with Cu–Au mineralization.
LA–ICP–MS zircon U–Pb dating yields mean ages of 117.
0 ± 2.
0 and 120.
9 ± 1.
7 Ma for ore‐bearing granodiorite porphyry and 105.
2 ± 1.
3 Ma for post‐ore basaltic andesite.
All the samples show high‐K calc‐alkaline compositions, with enrichment of light rare earth elements (LREE) and large ion lithophile elements (LILE: Cs and Rb) and depletion of high field strength elements (HFSE: Nb and Ti), consistent with the geochemical characteristics of arc‐type magmas.
Syn‐ and post‐ore volcanic rocks show initial Sr ratios of 0.
7045–0.
7055, εNd(t) values of −0.
8 to 3.
6, (206Pb/204Pb)t ratios of 18.
408–18.
642, (207Pb/204Pb)t of 15.
584–15.
672 and positive zircon εHf(t) values of 1.
3–10.
5, likely suggesting they dominantly were derived from metasomatized mantle wedge and contaminated by southern Qiangtang crust.
Compared to mafic volcanic rocks, barren and ore‐bearing granodiorite porphyries have relatively high initial Sr isotopic ratios (0.
7054–0.
7072), low εNd(t) values (−1.
7 to −4.
0), similar Pb and enriched zircon Hf isotopic compositions [εHf(t) of 1.
5–9.
7], possibly suggesting more contribution from southern Qiangtang crust.
Duolong volcanic rocks and granodiorite porphyries likely formed in a continental arc setting during northward subduction of the Bangong–Nujiang ocean and evolved at the base of the lower crust by MASH (melting, assimilation, storage and homogenization) processes.
Copyright © 2014 John Wiley & Sons, Ltd.
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