Evaluation of the properties of dolomitization fluids and diagenetic alterations of mg/Ca ratios in carbonate rocks in the cambrian series-2 to miaolingian strata in Central Uplift Belt, Tarim Basin: Constraints from halogens, REEs and isotope geochemistry

Abstract

The nature of the dolomitization fluids and the diagenetic alterations on carbonate Mg/Ca ratios in Cambrian series-2 to Miaolingian strata in Central Uplift Belt, Tarim Basin are interpreted on the basis of petrography, geochemistry (trace elements, halogens, REEs, O–C–Sr isotopes) and fluid inclusion microthermometry. Based on petrographic examination, two types of less stoichiometric dolomites: dolomicrites (DM), very fine-to fine-crystalline planar-e(s) dolomite (D1) formed at near-surface to shallow-burial settings, and two types of more stochiometric dolomites (fine-to medium-crystalline planar-e(s) dolomite (D2) and medium-to coarse-crystalline.nonplanar-a dolomite (D3)) formed at deep-burial setting are identified. Medium-to coarse-crystalline, nonplanar-a saddle dolomite cement (DC), and early-stage calcite cement (ESCAL) and later-stage calcite cement (LSCAL) are identified. The DM, D1, D2, and D3 samples display positive Cerium anomalies (δCe) and negative Europium anomalies (δEu), and the DC display positive δCe and positive δEu. They show micritic-bladed and blocky calcite-like REE patterns, suggesting their dolomitizing fluids inherited the seawater or seawater-like REE signatures of their precursor carbonate materials at the time of crystal growth. No correlations exist between δ13C, δ18O, 87Sr/86Sr, Mg/Ca, and Mn/Sr which were tools used to evaluate the diagenetic history of the carbonates, coupled with the high Mg/Ca ratios (0.64–0.85), Mn/Sr ratios, and more depleted δ18O, δ13C values of D2, D3, and DC. This suggests that the dolomites were altered by high-temperatures or their isotopic difference may be the result of equilibrium isotopic fractionation. The increasing trend in Cl/(Ca + Mg), I/(Ca + Mg), and Br/(Ca + Mg) ratios in the D2, D3, and DC with dolomite content >50 wt% can be explained by the presence of evaporite (salt) derived from seawater or sedimentary pore waters as fluid interaction with sedimentary materials in the studied strata. The comparable isotopic (δ18O, δ13C and 87Sr/86Sr) values between DM, D1, D2, D3, DC, and coeval Early Paleozoic seawater value, coupled with the relatively high homogenization temperature (Th) and salinity levels in D2, D3, and DC, indicates that their diagenetic fluids were derived from radiogenic 87Sr-enrich coeval seawater with hypersaline signatures in deep-burial settings. The dolomitization model shows that the precipitation of dolomicrites was by evaporative seepage-reflux dolomitization at near-surface burial settings. Evaporative seawater dolomitization supported by 87Sr/86Sr, δ13C values and calculated water oxygen isotope ratio was probably responsible for the D1 during shallow-burial, and D2 and D3 with irregular overgrowth rims were formed during deep-burial dolomitization. The average range of the Th values of DC is 148.2–193.4 °C; mostly overlapping with the estimated ambient temperature (65 °C–180 °C, at a depth >4000 m) for the studied strata, indicates that the growth of DC in fractures may have resulted from upward and laterally squeezed higher-temperature saline-enriched basinal fluids conveyed by geothermal convective-advective fluid flows or squeegee fluid flows at depth resulting in geothermal dolomitization.