Isotopic and Chemical Composition of the Deep Water of Lake Baikal

Introduction. Due to its natural composition, the deep water of Lake Baikal can be bottled without any conserving agents. The development of large-scale production of bottled Baikal water requires its detailed study in order to protect it from counterfeit and falsification. The purpose of this work was to study the isotopic and chemical composition of the deep water of Lake Baikal and offer indicators for its identification. Study objects and methods. The research included deep water of Lake Baikal, sampled at various points, the water from the Angara River, and the tap water from the cities of Irkutsk and Shelekhov. The tests were performed using a quadrupole ICP-MS mass spectrometer and a Delta V Plus isotope mass spectrometer with a GasBench II module. Results and discussion. All the water samples revealed fresh water with insignificant mineralization. As for salts, the deep water samples had a lower content of sodium and chlorides, as well as a higher content of silicon. As for metals, the deep water samples contained iron, manganese, copper, and zinc; in the tap water samples, these indicators were significantly higher. Unlike that of the Angara water samples, the isotopic profile of the deep water samples was somewhat “lighter”, both in the ratio of oxygen isotopes δ18O – by 0.73‰, and hydrogen δD – by 0.49‰. The tap water samples had a higher deuterium content. The content of oxygen isotopes (δ18O) in the tap water samples was close to that in the Angara samples. Conclusion. The complex physicochemical and isotope analyses expanded the list of identification indicators and made it possible to identify the deep water of Lake Baikal.

Hydrothermal Alteration and Its Superimposed Enrichment for Qianjiadian Tabular-Type Uranium Deposit in Southwestern Songliao Basin

The evolution characteristics of hydrothermal activity and superimposed uranium mineralization in the Qianjiadian ore field in southwestern Songliao Basin are still controversial and lack direct evidence. In this comprehensive study, a detailed identification of dolerite and hydrothermally altered un-mineralized sandstone and sandstone-hosted ore in the Yaojia Formation have been performed through the use of scanning electron microscopy observation, electron probe, carbon-oxygen-sulfur isotope, and fluid inclusion analyses. The results show that the hydrothermal fluid derived from the intermediate-basic magma intrusion is a low-temperature reducing alkaline fluid and rich in CO2, Si, Zr, Ti, Fe, Mg, Mn, and Ca, producing different types of altered mineral assemblages in the rocks, including carbonation, pyritization, sphalerite mineralization, clausthalite mineralization, silicification, and biotitization. Specifically, the carbonate minerals in sandstone are mixed products of deep hydrothermal fluid and meteoric water, with carbon and oxygen isotopes ranging from −5.2‰ to −1.7‰ and −20.4‰ to −11.1‰, respectively. Carbon source of the carbonate minerals in dolerite is mainly inorganic carbon produced at the late stage of intermediate-basic magma evolution, with carbon and oxygen isotopes from −16.1‰ to −7.2‰ and −18.2‰ to −14.5‰, respectively. Various carbonate minerals in the rocks may have been precipitated by the hydrothermal fluid after the magmatic stage, due to the change of its CO2 fugacity, temperature, and cation concentration during the long-term evolution stage. A series of carbonate minerals were generated as calcite, dolomite, ankerite, ferromanganese dolomite, and dawsonite. The precipitation processes and different types of carbonate mineral mixtures identified in this study mainly occur as parallel, gradual transition, interlacing, or inclusion metasomatism in the same vein body, without obvious mineralogical and petrologic characteristics of penetrating relationship. Homogenization temperature of fluid inclusions in calcite is high, in the range of 203–234 °C, with a low salinity of 0.71–4.34% NaCl, and the data range is relatively concentrated. Homogenization temperature of fluid inclusions in ankerite is usually low, ranging from 100 °C to 232 °C, with a high salinity of 4.18–9.98% NaCl. The precipitation processes of carbonate minerals and the results of this study are basically in consistent. Overall, the sandstone-type uranium deposits have a temporal and genetic relationship with hydrothermal activities during Paleogene. (1) Hydrothermal activity was directly involved in uranium mineralization, result in dissolution and reprecipitation of earlier uranium minerals, forming uranium-bearing ankerite and complexes containing uranium, zirconium, silicon, and titanium. (2) Hydrothermal fluid activity provided reducing agent to promote hydrocarbon generation from pyrolysis of carbonaceous fragments and accelerate uranium precipitation rate. (3) Regional water stagnation prolongs reaction time, contributing to huge uranium enrichment. This study provides new petrologic, mineralogical, and geochemical evidence for multi-fluid coupled and superimposed mineralization of sandstone-hosted uranium deposits in the sedimentary basin.

Geochemical Characteristics and Origin of Formation Water From the Upper Triassic Xujiahe Tight Sandstone in the Xiaoquan-Fenggu Structural Belt, Western Sichuan Depression, China

Formation water represents an important driving force and carrier for the migration and accumulation of oil and gas; thus, research on its origin is a hot spot in petroleum geology. The Upper Triassic Xujiahe Formation in the Xiaoquan-Fenggu Structural Belt in the western Sichuan Depression, China, has developed thick tight sandstone gas reservoirs. However, previous studies have provided different conclusions on the origin of the formation water in the Xujiahe tight sandstone reservoir. In this paper, the origin of the formation water in the Xujiahe Formation was determined based on the latest major and minor elemental concentration data, hydrogen and oxygen isotopes data of formation water, and carbon and oxygen isotope data of carbonate cements. The results show that the salinity of the formation water of the Xujiahe Formation in the study area is generally greater than 50 g/L. The water type is mainly the CaCl2 type, although a small proportion of NaHCO3 type water with high salinity is observed, which is related to hydrocarbon expulsion by overpressure. Moreover, the formation water in the sandstone of the Xujiahe Formation is obviously rich in Br, which is related to membrane infiltration, overpressured hydrocarbon expulsion of shale and diagenesis of organic matter. The composition of Cl− and Na+ ions in the formation water in the Xujiahe tight sandstone reservoir is consistent with the seawater evaporation curve, which deviates significantly from the freshwater evaporation curve. The hydrogen and oxygen isotopes of condensate water in the Xujiahe Formation tight sandstone are similar to those of atmospheric precipitation water, while the hydrogen and oxygen isotopes of the formation water in the Xujiahe Formation show that it is of seawater origin. Therefore, to use hydrogen and oxygen isotopes to determine the origin of formation water, condensate water must be accurately differentiated from formation water. Otherwise, if the condensate water is misjudged as formation water, then incorrect conclusions will be drawn, e.g., that the formation water of the Xujiahe Formation originated from fresh water. Affected by organic carbon, the carbon isotope Z value of the carbonate cements in the Xujiahe Formation is low (mainly distributed between 110 and 130). A Z value of less than 120 does not indicate that the ancient water bodies formed by cements were fresh water or mixed water bodies. However, Z values greater than 120 correspond to a formation temperature lower than 80 C, which indicates that carbonate cement was not affected by organic carbon; thus, the Z value can reflect the origin of ancient water bodies. The results of this study indicate that the formation water of the Xujiahe tight sandstone in the study area is of seawater origin. The determination of the origin of the formation water and seawater of the Xujiahe Formation provides strong evidence for the determination of the marine sedimentary environment of the Xujiahe Formation in the study area, and can provide scientific guidance for the search for high-quality reservoirs.

Chronology, time averaging, and oxygen isotope composition of harvested marine mollusk assemblages from Ifri Oudadane, northeast Morocco

The archaeological site of Ifri Oudadane, NE Morocco, contains well-preserved marine mollusk concentrations throughout the Epipaleolithic (hunting-gathering) and Neolithic (food production) cultural phases, useful to test hypotheses driving such transition. However, the chronology and stratigraphy of harvested shells is complex due to the confluence of human activity and natural deposition processes. This work first quantifies the age and degree of time averaging of archaeological shells and then estimates sea-surface temperatures (SSTs) from the oxygen isotopes of selected specimens. Thirty-four radiocarbon-dated shells exhibited significant time averaging between 310 to 1170 yr that could not be explained by analytical error alone. This finding illustrates the need for individually dating shells in future paleoclimate investigations aiming for high temporal resolution. Nine isotopically analyzed shells dated to the Neolithic phase, between 5700 and 7600 cal yr BP, indicate that assuming constant oxygen isotopes of seawater, SSTs remained consistently warm, between 20°C and 22°C, that is, 2°C–4°C warmer than today. Results point to warmer conditions during the Neolithic, supporting the hypothesis that the rise of a food production mode of life in NE Morocco could have in part been triggered by warming conditions following the colder 8.2 event.