Geochemical studies, magmatic evolution, microstructures and replacement mechanisms in Jebale-Barez granitoid Complex (East and Southeast Jiroft)

IntroductionThe Jebale-Barez Plutonic Complex (JBPC) is composed of many intrusive bodies and is located in the southeastern province of Kerman on the longitude of the 57◦ 45 ' east to 58◦ 00' and Northern latitudes 28◦ 30' to 29◦ 00'. The petrologic composition is composed of granodiorite, quartzdiorite, granite, alkali-granite, and trace amounts of tonalite with dominant granodiorite composition. Previously, the JBPC was separated into three plutonic phases by Ghorbani (2014). The first plutonic phase is the main body of the complex with composition of quartz-diorite to granodiorite. After differentiation of magma in the magmatic chamber, the porphyritic and not fully consolidated magmas have intruded into the main body. Their compositions were dominantly granodiorite and granite that are defined as the second plutonic phase. Finally, the last phase was started by an intrusion of the holo- leucogranite into the previous bodies. This plutonic activity was pursued by the minor Quaternary basaltic volcanism that shows metamorphic haloes in the contacts. They are dominantly porphyric leucogranites. However, some bodies show dendritic texture that may imply the existence of silicic fluids in the latest crystallization stages.
Materials and methodsIn this article different analysis methods were used. For example, we used a total of two hundred samples of the various granitoids that were selected for common thin section study. Forty four representative samples from the different granitic rocks were selected for whole rock chemical analyses. The analyses of both major and trace elements were performed at the Department of Earth Sciences, the University of Perugia, Italy. The analysis for all major elements was carried out by an X-ray fluorescence spectrometry (XRF) using a tube completed with a Rn and W anode under conditions with acceleration voltage of 40-45 kV and electric current ranging from I=30-35 mA. After calcination of powdered samples and full matrix correction, the sum of all major oxides was equal to about 100 wt.%. The concentration of trace elements in the selected samples has been performed by Inductively Coupled Plasma-Mass Spectrometry (ICP-MS). The uncertainty is