Mixing of cogenetic magmas in the Cretaceous Zhangzhou calc-alkaline granite from SE China recorded by in-situ apatite geochemistry

2021 ◽  
Author(s):  
S. Aspiotis ◽  
S. Jung ◽  
F. Hauff ◽  
R. L. Romer

AbstractThe late-tectonic 511.4 ± 0.6 Ma-old Nomatsaus intrusion (Donkerhoek batholith, Damara orogen, Namibia) consists of moderately peraluminous, magnesian, calc-alkalic to calcic granites similar to I-type granites worldwide. Major and trace-element variations and LREE and HREE concentrations in evolved rocks imply that the fractionated mineral assemblage includes biotite, Fe–Ti oxides, zircon, plagioclase and monazite. Increasing K2O abundance with increasing SiO2 suggests accumulation of K-feldspar; compatible with a small positive Eu anomaly in the most evolved rocks. In comparison with experimental data, the Nomatsaus granite was likely generated from meta-igneous sources of possibly dacitic composition that melted under water-undersaturated conditions (X H2O: 0.25–0.50) and at temperatures between 800 and 850 °C, compatible with the zircon and monazite saturation temperatures of 812 and 852 °C, respectively. The Nomatsaus granite has moderately radiogenic initial 87Sr/86Sr ratios (0.7067–0.7082), relatively radiogenic initial εNd values (− 2.9 to − 4.8) and moderately evolved Pb isotope ratios. Although initial Sr and Nd isotopic compositions of the granite do not vary with SiO2 or MgO contents, fSm/Nd and initial εNd values are negatively correlated indicating limited assimilation of crustal components during monazite-dominated fractional crystallization. The preferred petrogenetic model for the generation of the Nomatsaus granite involves a continent–continent collisional setting with stacking of crustal slices that in combination with high radioactive heat production rates heated the thickened crust, leading to the medium-P/high-T environment characteristic of the southern Central Zone of the Damara orogen. Such a setting promoted partial melting of metasedimentary sources during the initial stages of crustal heating, followed by the partial melting of meta-igneous rocks at mid-crustal levels at higher P–T conditions and relatively late in the orogenic evolution.


2020 ◽  
Vol 117 (35) ◽  
pp. 21125-21131 ◽  
Author(s):  
Jing-Liang Guo ◽  
Zaicong Wang ◽  
Wen Zhang ◽  
Frédéric Moynier ◽  
Dandan Cui ◽  
...  

Zircons widely occur in magmatic rocks and often display internal zonation finely recording the magmatic history. Here, we presented in situ high-precision (2SD <0.15‰ for δ94Zr) and high–spatial-resolution (20 µm) stable Zr isotope compositions of magmatic zircons in a suite of calc-alkaline plutonic rocks from the juvenile part of the Gangdese arc, southern Tibet. These zircon grains are internally zoned with Zr isotopically light cores and increasingly heavier rims. Our data suggest the preferential incorporation of lighter Zr isotopes in zircon from the melt, which would drive the residual melt to heavier values. The Rayleigh distillation model can well explain the observed internal zoning in single zircon grains, and the best-fit models gave average zircon–melt fractionation factors for each sample ranging from 0.99955 to 0.99988. The average fractionation factors are positively correlated with the median Ti-in-zircon temperatures, indicating a strong temperature dependence of Zr isotopic fractionation. The results demonstrate that in situ Zr isotope analyses would be another powerful contribution to the geochemical toolbox related to zircon. The findings of this study solve the fundamental issue on how zircon fractionates Zr isotopes in calc-alkaline magmas, the major type of magmas that led to forming continental crust over time. The results also show the great potential of stable Zr isotopes in tracing magmatic thermal and chemical evolution and thus possibly continental crustal differentiation.


2021 ◽  
Author(s):  
Long Zhang ◽  
Zhenyu Chen ◽  
Fangyue Wang ◽  
Noel C. White ◽  
Taofa Zhou

Abstract Uraninite is the main contributor to the bulk-rock uranium concentration in many U-rich granites and is the most important uranium source for granite-related uranium deposits. However, detailed textural and compositional evolution of magmatic uraninite in granites during alteration and associated uranium mobilization have not been well documented. In this study, textures and geochemistry of uraninites from the Zhuguangshan batholith (South China) were investigated by scanning electron microscopy (SEM) and electron probe microanalysis (EPMA). The geochemical data indicate that the Longhuashan and Youdong plutons are peraluminous leucogranite, the Changjiang pluton is highly fractionated high-K calc-alkaline granite, and the Jiufeng pluton belongs to a high-K calc-alkaline association. Uraninites from the Longhuashan and Youdong granites have lower concentrations of ThO2 (0.9–4.0 wt %) and rare earth elements (REE)2O3 (0.1–1.0 wt %) than those from the Changjiang and Jiufeng granites (ThO2 = 4.4–7.6 wt %, REE2O3 = 0.7–5.1 wt %). Uraninites observed in the Longhuashan, Youdong, Changjiang, and Jiufeng granites yielded chemical ages of 223 ± 3, 222 ± 2, 157 ± 1, and 161 ± 2 Ma, respectively. The samples (including altered and unaltered) collected from the Longhuashan, Youdong, and Changjiang granites are characterized by highly variable whole-rock U concentrations of 6.9 to 44.7 ppm and Th/U ratios of 0.9 to 7.0, consistent with crystallization of uraninite in these granites being followed by uranium leaching during alteration. Alteration of uraninite, indicated by altered domains developing microcracks and appearing darker in backscattered electron (BSE) images compared to unaltered domains, results in the incorporation of Si and Ca and mobilization of U. In contrast, the least altered samples of the unmineralized Jiufeng granite have low U concentrations (5.3–16.4 ppm) and high ΣREE/U (13.6–49.4) and Th/U ratios (2.1–5.6), which inhibit crystallization of uraninite, as its crystallization occurs when the U concentration is high enough to exceed the substitution capacity of other U-bearing minerals. These results indicate that the Longhuashan, Youdong, and Changjiang granites were favorable uranium sources for the formation of uranium deposits in this area. This study highlights the potential of uraninite alteration and geochemistry to assist in deciphering uranium sources and enrichment processes of granite-related uranium deposits.


2002 ◽  
Vol 66 (2) ◽  
pp. 235-251 ◽  
Author(s):  
X. Wang ◽  
W. L. Griffin ◽  
S. Y. O’Reilly ◽  
X. M. Zhou ◽  
X. S. Xu ◽  
...  

AbstractThe Pingtan and Tonglu igneous complexes in SE China are typical of the calc-alkaline series developed at active continental margins. These two complexes are dominated by felsic rocks, temporally and spatially associated with minor mafic rocks. Morphological and trace-element studies of zircon populations in rocks from each of these complexes show that the zircon populations may be divided into 3–4 distinct growth stages, characterized by different distributions of morphological indices (Ipr, Ipy and Iel), and different contents of the substituting elements (Hf, U, Th, Y and P). The four growth stages recognized in the zircons are believed to have formed successively in the magma chamber, during the emplacement, and in the early and later stages of magma consolidation, respectively. All four stages are recognized in the plutonic Pingtan complex, whereas the stages 3 and 4 are less developed in the volcanic/subvolcanic Tonglu complex. Based on the chemistry and morphology of the different zircon populations of the Pingtan and Tonglu complexes, it is suggested that basaltic magmas underplating at the boundary between crust and mantle caused partial melting of the mid–lower crust and produced granitoid magmas. Subsequently, mixing between magmas was important.


2015 ◽  
Vol 27 (1) ◽  
pp. 258-280 ◽  
Author(s):  
Laura Iudith Bellos ◽  
Antonio Castro ◽  
Juan Díaz-Alvarado ◽  
Alejandro Toselli
Keyword(s):  

1982 ◽  
Vol 46 (339) ◽  
pp. 201-210 ◽  
Author(s):  
Agnete Steenfelt

AbstractThe Caledonian fold belt of East Greenland contains calc-alkaline granite (sensu lato) intrusions with ages ranging from c.2000 Ma to c.350 Ma. The Proterozoic granites have low U contents and the pre-Devonian Caledonian granites contents of U corresponding to the clarke value for U in granites. Some aspects of the geochemistry of U are discussed using U-K/Rb, U-Sr, U-Zr, and U-Th diagrams. Secondary enrichment and mineralization occurs in fractured and hydrothermally altered granites and rhyolites situated in or near a major NNE fault zone. The U is associated with iron oxides or hydrocarbons. It is suggested that the source of the mineralization was Devonian acid magma, which also acted as a heat source for circulating hydrothermal fluids.


1984 ◽  
Vol 74 (4) ◽  
pp. 193-227 ◽  
Author(s):  
N. M. S. Rock

ABSTRACTCalc-alkaline lamprophyres are porphyritic dyke-rocks, richer in amphibole, biotite, ultramark elements (Mg, Cr, Ni) and incompatible elements (K, F, P, Rb, Sr, Zn, Nb, Ba, REE, Th, U) than other rocks of comparable colour index (35–67) or % SiO2(46–57). Field and petrological criteria are suggested for identifying them uniquely. New average compositions, based on some 600 screened analyses, confirm the chemical variability but possible heteromorphism of vogesites, kersantites, spessartites and some minettes. Calc-alkaline lamprophyres probably crystallise from volatile-rich, crystal-laden fluids. Microdioritic ‘porphyrites’, K-rich syenites and quartz-feldspar porphyries commonly form from these fluids by acidic hybridisation, and more rarely byin situdifferentiation. Calc-alkaline lamprophyres have close compositional equivalents among, for example, shonkinites and absarokites, but not among kimberlites or common plutonie or volcanic rocks. They are compositionally more ‘crustal’ than lamproites and leucitites, despite some overlap. They are far more widespread than other K-rich or alkaline rocks. Three genetic petrological associations are confirmed: with calc-alkaline granitoid plutons (A), with shoshonitic volcanic and subvolcanic suites (B), and with appinite—breccia-pipe complexes (C). Most calc-alkaline lamprophyres, from association A, perhaps form by crustal modification of primary lamproitic or leucititic magmas; a very few, carrying rare mantle-type xenoliths, may represent relatively unmodified, but otherwise similar, primary magmas. Those of association B may form merely by volatile enrichment of shoshonitic magmas during subvolcanic crystallisation. Different origins for minettes in these associations are suggested by compositional differences, revealed by discriminant analysis.


2009 ◽  
Vol 260 (1-2) ◽  
pp. 73-86 ◽  
Author(s):  
Courtney J. Gregory ◽  
Christopher R.M. McFarlane ◽  
Jörg Hermann ◽  
Daniela Rubatto

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