We compare the petrogenetic and chemical signatures of two alkali silicate suites from the Cretaceous Damaraland igneous province (Namibia), one with and one without associated carbonatite, in order to explore their differences in terms of magma source and evolution. The Etaneno complex occurs in close spatial proximity to the Kalkfeld bimodal carbonatite–alkali silicate complex, and is dominated by nepheline (ne)-monzosyenites and ne-bearing alkali feldspar syenites. The Etaneno samples have isotopic compositions of 87Sr/86Sr(i)=0.70462–0.70508 and Nd=−0.5 to −1.5, with the highest 87Sr/86Sr(i) and lowest Nd values observed in evolved samples. The magma differentiated via olivine, feldspar, clinopyroxene, and nepheline (ne) fractionation in a F-rich system, which fractionated Zr from Hf, and Y from Ho. Partly glassy, recrystallized inclusions in some samples are less evolved than their host rocks and contain a cumulate component (nepheline, plagioclase). The Kalkfeld ne-foidites (ijolites) and ne-syenites have 87Sr/86Sr(i)=0.70285–0.70592 and Nd=0.5 to 1.1. The isotope ratios show no consistent variation with rock composition, and they are in the same range as the associated carbonatites. The Kalkfeld silicate magma fractionated nepheline and alkali-feldspar in a CO2-dominated, F- and Ca-poor system. As a result, the rocks display some major and trace element trends distinctly different from those of the Etaneno samples.
We suggest that the Etaneno and the Kalkfeld magmas represent different melt fractions of a heterogeneous mantle source, resulting in different compositions especially with respect to CO2 contents of the primitive, parental magmas. In this scenario, the carbonated alkali silicate Kalkfeld parental melt contained a critical CO2 concentration and underwent liquid separation of carbonate and silicate melt fractions at crustal depths. The resulting silicate melt fraction experienced a very different mode of differentiation than the carbonate-poor Etaneno parental magma. Thus, the Kalkfeld rocks are depleted in Ca and other divalent cations, as well as F, rare-earth elements (REE), Ba, and P relative to the Etaneno syenites. We interpret these differences to reflect the partitioning of these elements into the carbonate melt fraction during immiscible separation. 相似文献
Abstract Whole—rock Rb—Sr, zircon U—Pb and hornblende, biotite and K—feldspar K—Ar ages are used to reconstruct the cooling history of the Huangmeijian intrusion in the Anqing—Lujiang quartz—syenite belt in Anhui. Oxygen isotope geothermometry of mineral pairs demonstrates that diffusion is a dominant factor controlling the closure of isotopic systems. Assuming the cooling of the intrusion is synchronous with a dicrease in local geothermal gradients, an emplacement depth of about 8 km and the magma crystallization temperature of 800 ± 50°C are estimated. The Huangmeijian intrusion experienced a rapid cooling process and uplifted after its emplacement and crystallization at 133 Ma B.P. with a cooling rate of 34.5°C / Ma and an uplifting rate of 0.35 mm/ a. The intrusion was rising until it rested at a depth of 3 km at a temperature of 300 ± 50°C about 14 Ma later. Then the intrusion was in slow cooling and uplifting with a cooling rate of 4.4°C / Ma and an uplifting rate of 0.04 mm/ a. U—Pb dating of pitchblende is done for the hydrothermal uranium deposit formed in the contact zone of the Huangmeijian intrusion. The result shows that the mineralization age is close to the closing time of the K—Ar system in biotite. The fluid inclusion thermometry indicates that the mineralization temperature is in agreement with the closure temperature of the biotite K—Ar system. This suggests a close relationship between the slow cooling of the intrusion and the hydrothermal uranium mineralization process. 相似文献