Celestine Mineralisation in Jabal Hafit, Al-Ain (United Arab Emirates): Constraints from Geochemical and Sr-S Isotope Systematics

Celestine (SrSO4) is the principal ore of Sr and a sensitive tracer of diagenetic fluid–rock interaction in carbonate–evaporite successions. This study presents integrated petrographic mineral chemistry and Sr–S isotopic data for epigenetic celestine hosted by Asmari carbonates at Jabal Hafit, Al Ain (UAE), to constrain fluid source, and mechanisms of SrSO4 precipitation during basin diagenesis. Field and SEM observations show celestine as stratabound, vug- and fracture-filling euhedral to subhedral crystals within dolomitised limestone, suggesting precipitation after initial lithification during early-to-mid burial diagenesis. Electron microprobe analyses show nearly stoichiometric SrSO4 (55.15–57.30 wt.% SrO; 42.43–44.35 wt.% SO3) with very low Ba and Ca. The characteristically high Sr/Ba signature of the celestine reflects a complex diagenetic history driven by efficient Sr remobilisation during carbonate recrystallisation within an inherently Ba-poor marine sequence. Measured 87Sr/86Sr ratios are tightly clustered (0.707841–0.707854) with a high degree of isotopic homogeneity, which indicates a stable, well-buffered fluid reservoir, while the absolute values align with an Oligocene marine signature. Sulphur isotope values (δ34S = +27.3 to +29.1‰) are enriched relative to coeval marine sulphate, which could be attributed to closed-system Rayleigh fractionation driven by bacterial sulphate reduction. We propose that celestine precipitated from stable, marine-buffered burial brines, where supersaturation was achieved through coupled Sr enrichment from carbonate diagenesis and microbial modification of the sulphate reservoir.

Minerals

Minerals

16

2075-163X

N/A

6

18