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Travertines formed of crystalline crust have been widely reported, but there has not been focus on their geochemical characteristics. We therefore carefully conducted a series of geochemical investigations and U-Th dating on a travertine mound mainly composed of crystalline crust from Sobcha (southwest China) to determine their geochemical features and geological implications. The Sobcha travertines dominantly consist of granular crystals and fan crystals and show δ13C from 3.4‰ to 4.9‰ V-PDB, δ18O from −26.7‰ to −23.7‰ V-PDB, and 87Sr/86Sr from 0.712458 to 0.712951. When normalized to PASS, the Sobcha travertines exhibit MREE enrichment relative to HREE and LREE, HREE enrichment relative to LREE, and positive Eu anomalies. The δ13C signatures and mother CO2 evaluation of the Sobcha travertines show that the Sobcha travertines were thermogene travertines largely receiving mother CO2 from (upper) mantle (i.e., magmatic CO2) or a mixture of soil-derived CO2 and CO2 related to carbonate decarbonation. The 87Sr/86Sr of the Sobcha travertines is out of the 87Sr/86Sr ranges of local deposits exposed at Sobcha and surrounding areas but is well matched with the mean 87Sr/86Sr of Nadi Kangri volcanic rocks which cropped out to the northeast of the studied travertines (over 20 km away). This might indicate the important role of the Nadi Kangri volcanic rocks in suppling Sr to the studied travertines, but more studies are required. The LREE depletion compared to MREE and HREE in the Sobcha travertines was interpreted to be caused by the difference in geochemical mobility between LREEs and HREEs during water–rock interaction at depth, while the MREE enrichment compared to HREE was considered to be most likely inherited from reservoir/aquifer rocks. The positive Eu anomalies of the Sobcha travertines may result from very high reservoir temperatures and/or preferential dissolution of Eu-rich minerals/rocks (especially plagioclase). The Sobcha travertine mounds displays no or very slight vertical variations in δ13C, 87Sr/86Sr, and REE patterns, indicating the compositional stability of mother CO2 and paleo-fluids. However, a significant vertical increase in δ18O was observed and was explained as the result of gradual water temperature decrease related to climate cooling, self-closure of the vents, or mound vertical growth. The findings in this study might help us better understand the deposition of crystalline crust in Ca2+-deficient hot spring systems. [ABSTRACT FROM AUTHOR]

Banded travertines are important parts of fissure ridge systems, but studies on geochemical characterization of banded travertines are limited. This study investigated the lithofacies and stable carbon and oxygen isotopic features of banded travertines from Xiagei (southwestern China) to examine their formation mechanisms. Petrographic analyses of the banded travertines revealed two lithotypes: thick-laminated palisade crystalline crust and thin-laminated composite crystalline crust. δ13C and δ18O of the Xiagei banded travertines range from 2.82‰ to 4.50‰ V-PDB, and from −25.86‰ to −20.90‰ V-PDB. Parent CO2 evaluation shows that the Xiagei banded travertines mainly received CO2 from the decarbonation of marine carbonates, but the contributions of magmatic CO2 and the dissolution of marine carbonates are also unneglectable. Significantly, the magmatic-derived CO2 might indicate that the delamination of the lithosphere along with the asthenosphere upwelling could be taking place in the eastern Tibetan plateau. Paleotemperature calculation shows that the Xiagei travertines were precipitated from moderate- to high-temperature hot springs (44.3 to 86.8 °C). Interestingly, the thick-laminated palisade crystalline crust and thin-laminated composite crystalline crust display calculated paleotemperature between 66.6 and 86.8 °C and between 56.6 and 77.7 °C, respectively, reflecting the great role of water temperature in controlling the lithofacies of banded travertines. A comparison between the banded travertines at Xiagei and other areas also shows temperature is a non-negligible factor controlling banded travertine precipitation. However, this does not mean that water temperature is the decisive controlling factor and more studies on banded travertines are still indispensable to disclose the potential factors controlling the factors/processes affecting banded travertine lithofacies. This study provides a good example for understanding the relationship between lithofacies and stable isotopic geochemical characteristics of travertine deposits. [ABSTRACT FROM AUTHOR]

The Middle-Upper Cambrian Xixiangchi Formation in the Sichuan Basin is regarded as an important reservoir with great potential for hydrocarbon exploration. It is previously indicated that the Xixiangchi carbonates have experienced extensive dolomitization, however, the origin of dolomitizing fluids and the dolomitization mechanism still remain uncertain. In this study, a set of petrographic and geochemical examinations, including rare earth elements (REE) and isotopic (C, O, and Sr) compositions were used to trace the origins of dolomitizing fluids and associated diagenetic processes. The petrographic examination revealed three types of matrix dolomites (D1, D2, D3) and one cement saddle dolomite (SD). These phases have crystal size ranges of less than 30 μm (very fine to fine crystals, D1), 30–100 μm (fine to medium crystals, D2), 100–300 μm (medium to coarsely crystalline dolomite, D3), and 0.3–4 mm (fracture filling cements, SD), respectively. D1 is characterized by non to very weak luminescence, weakly negative Ce anomalies (Ce/Ce* = 0.84 ± 0.02), strongly negative Eu anomalies (Eu/Eu* = 0.65 ± 0.03), and high 87Sr/86Sr ratios (0.71062 ± 0.00122). In combination with δ13C (−1.5‰ ± 0.2‰) and δ18O (−9.7‰ ± 0.5‰) compositions, D1 is interpreted to be formed by penecontemporaneous dolomitization in the near-surface environment with seawater as the dolomitizing fluid. In contrast, D2 is characterized by intercrystalline pores, dirty crystal surfaces, similar δ13C (−1.4‰ ± 0.4‰) compositions but higher δ18O (−8.9‰ ± 0.7‰) compositions, and lower 87Sr/86Sr ratios (0.70992 ± 0.00035), similar Ce anomalies (Ce/Ce* = 0.87 ± 0.04) and higher Eu anomalies (Eu/Eu* = 0.85 ± 0.04). The coarser D2 is regarded to be formed by the post-penecontemporaneous seepage-reflux dolomitization or by recrystallization of D1 dolomite in a near-surface or shallow burial environment. D3 is distinguished by a cloudy core with clear rims, showing slightly higher Eu anomalies (Eu/Eu* = 0.88 ± 0.02) and similar Ce anomalies (Ce/Ce* = 0.88 ± 0.02) than those of D1 and D2. Combined with the δ18O compositions (−10.4‰ ± 0.4‰) and 87Sr/86Sr ratios (0.70989 ± 0.00048), D3 is thought to be formed by the overgrowth or recrystallization of D1 and D2 dolomites in a shallow to moderate burial environment. The fractures filling SD dolomite consists of nonplanar and much coarser crystals with undulatory extinctions and brighter red luminescence. The lower δ18O (−11.1‰ ± 0.3‰) compositions, lower negative Eu anomalies (Eu/Eu* = 0.70 ± 0.01) of SD than the matrix dolomites, and similar Ce anomalies (Ce/Ce* = 0.83 ± 0.01) are indicative of hydrothermal dolomitization, with possible fluids associated with the magma during the period of Emei taphrogenic movement. In addition, the 87Sr/86Sr ratios (0.70941 ± 0.00003) of SD suggest probable origin from the coeval seawater partially. Therefore, SD dolomite is interpreted to be formed by hydrothermal dolomitization with mixed dolomitizing fluid of seawater and hydrothermal fluids. In summary, all the matrix dolomites have almost the same ΣREE concentrations and exhibit similar near-flat REE partition patterns with weak LREE enrichments, weakly negative Ce anomalies, and negative Eu anomalies. Such characteristics of REE compositions are indicative of similar evolved dolomitizing fluid, such as seawater or seawater- derived fluids. By contrast, SD dolomites have a different REE partition pattern with left-leaning characteristics, LREE depletions, and negative Eu anomalies, thus suggesting a different dolomitizing fluid source from the matrix dolomites. In addition, the development of intercrystalline pores associated with D2 dolomite makes it more likely to be a potential reservoir, indicating that the dolomitizing history of carbonate has a strong influence on the quality of potential dolomite reservoirs. [ABSTRACT FROM AUTHOR]