International audienceThe geology of the Republic of Djibouti, in the SE Afar Triangle, is characterized by intense tectonic and bimodal volcanic activity that began as early as 25-30 Ma. Each magmatic event was accompanied by hydrothermal activity. Mineralization generally occurs as gold-silver bearing chalcedony veins and is associated with felsic volcanism. Eighty samples from mineralized hydrothermal chalcedony, quartz ± carbonate veins and breccias were studied from ten sites representing four major volcanic events that range in age from early Miocene to the present. The most recent veins are controlled by fractures at the edges of grabens established during the last 4 Myr. Gold in excess of 200 ppb is present in 30% of the samples, with values up to 16 ppm. Mineralogical compositions allowed us to identify different types of mineralization corresponding to different depths in the hydrothermal system: (1) surface and subsurface mineralization characterized by carbonate chimneys, gypsum, silica cap and quartz ± carbonate veins that are depleted in metals and Au; (2) shallow banded chalcedony ± adularia veins related to boiling that contain up to 16 ppm Au, occurring as native gold and electrum with pyrite, and tetradymite; (3) quartz veins with sulfides, and (4) epidote alteration in the deepest hydrothermal zones. Samples in which pyrite is enriched in As tend to have a high Au content. The association with bimodal volcanism, the occurrence of adularia and the native Au and electrum in banded chalcedony veins are typical of epithermal systems and confirm that this type of mineralization can occur in a young intracontinental rift system
Epithermal mineralization was recently described in synrift volcanic rocks from the SE Afar Rift in Djibouti. To infer fluid sources in this system, coupled sulfur and strontium isotopic analyses were performed on mineralized samples from hydrothermal veins and stockwork zones. Mineralization includes gypsum and chalcedony, and/or quartz ± carbonate containing gold and sulfides. Sulfur isotopic compositions of sulfides and sulfates were determined using Multicollector-Inductively Coupled Plasma Mass Spectrometer (MC ICPMS); Laser Ablation MC ICPMS; and Continuous Flow Elemental Analyzer-Isotope Ratio Mass Spectrometry while strontium isotopes were determined by Thermal Ionisation Mass Spectrometry (TIMS) methods. Sulfur isotopic composition of sulfides (mainly pyrite) varies from − 9.2 to + 6.6‰. These values are classically reported for hydrothermal sulfides resulting from the mixing of variable S sources such as seawater sulfate and magmatic source. In addition, individual pyrite grains within the same sample show both positive and negative δ34S values suggesting multi-phase mineralization processes. Coupled sulfur and strontium isotopic compositions of seven sulfate samples hosted in (i) gypsum mound, (ii) evaporites, (iii) stockwork veins in sediments or in volcanic rocks were also investigated to characterize the sources of Sr and S. The δ34S values of the sulfate ranged from − 0.8 to + 14.3‰ while the 87Sr/86Sr ranged from 0.70389 to 0.70639 consistent with variable mixing ratios of Sr and S derived from volcanic sources and seawater-derived sulfate. This study shows that, although precious-metal deposition is related to low-sulfidation epithermal environment, both acidic fluid of magmatic and saline origins contributed to the hydrothermal system in the SE Afar Rift. Please note that this is an author-produced PDF of an article accepted for publication following peer review. The definitive publisher-authenticated version is available on the publisher Web site.
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