The oxygen isotopic composition of carbonate in lakes has been used as a useful indicator in Palaeolimnological research, and has made some important contributions to our understanding of lacustrine systems. For modern lakes in arid or cold areas, however, there are few data available to test the effect of lake salinity and temperature on the oxygen isotopic composition of various carbonate sources such as ostracod, bulk carbonate, and fine-grained carbonate (< 60 μm). Here we examined the oxygen isotopic composition of ostracods, bulk carbonate, and fine-grained carbonates, as well as that of coexisting water from Lake Qinghai and the smaller surrounding lakes and ponds on the Qinghai–Tibet Plateau. Our investigation highlights three key effects. First, the oxygen isotopic composition of ostracods, bulk carbonate, and fine-grained carbonate in the lakes and ponds shows a clear response to lake water δ18O values, and these vary with water salinity. The relationship between lake water δ18O and salinity is not only dominated by the evaporation/freshwater input ratios, but is also controlled by the distance to the mouth of the major rivers supplying to the lake. Second, the ostracod, bulk carbonate, and fine-grained carbonate show similar isotopic change trends in the study area, and oxygen isotopic differences between ostracods and authigenic carbonate may be explained by the different water temperatures and very small ‘vital offsets’ of ostracods. Finally, the effect of water depth on temperature leads to increasing δ18O values in carbonates as water depth increases, both in benthic ostracods living on the lake bottom, as well as in bulk carbonate precipitated at the water surface.For arid, high-altitude Lake Qinghai, our results suggest that variations in the δ18O values of carbonate in Lake Qinghai are mainly controlled by the oxygen-isotope ratio of the lake water changing with water salinity. As a secondary effect, increasing water depth leads to cooler bottom and surface water, which may result in more positive δ18O values of ostracod and bulk carbonate. 相似文献
Geotechnical and Geological Engineering - Underground water-sealed storage cavern is an important way for petroleum strategic reserve in China, which owns lots of outstanding advantages, such as... 相似文献
It is universally known that residual soils behave very differently from sedimentary soils. While the latter is widely known as cross-anisotropic, little is known regarding the strength anisotropy of residual soils. This study presents how the inherent anisotropy affects the strength of natural granite residual soils under generalized conditions, where intact specimens were carefully prepared and sheared under triaxial compression, extension, simple shear, and hollow cylinder torsional shear tests. The strength of natural residual soil, in terms of ultimate stress ratio M and undrained shear strength Su, is found to be significantly anisotropic in a different way from normally consolidated clays with the maximum strength obtained under triaxial compression and the minimum under simple shear or at intermediate principal stress direction. As a result, the existing method failed to measure the anisotropy degree of the studied soil. Two parameters were proposed accordingly to quantify the anisotropic strength under general conditions, taking the special strength anisotropy pattern and cohesive-frictional nature of GRS into account. The proposed parameters enable the direct comparison of strength anisotropy among soils. This study serves as a data set to better understand residual soils regarding their anisotropic behaviors under generalized conditions. Although specific to granite residual soils in China, this study is expected to be more widely applicable to other weathered geomaterials.
To characterize the hydrothermal processes of East Pacific rise at 9°-10°N, sulfide mineral compositions, textural, and geochemical features of chimney ores were studied using ore microscope,scanning electron microscope, X-ray diffraction analysis, and electron microprobe techniques. Results show that there are three mineral assemblages for the hydrothermal chimney ores, namely:(i) anhydrite + marcasite + pyrite, (ii) pyrite + sphalerite + chalcopyrite, and (iii) chalcopyrite + bornite + digenite + covellite. Mineral assemblages, zonational features, and geochemical characteristics of the ore minerals indicate that ore fluid temperature changed from low to high then to low with a maximum temperature up to 400 ℃. The chimney is a typical black smoker. The initial structure of the chimney was formed by the precipitation of anhydrites, and later the sulfides began to precipitate in the inner wall. 相似文献
The Fengjia barite–fluorite deposit in southeast Sichuan is a stratabound ore deposit which occurs mainly in Lower Ordovician carbonate rocks. Here we present results from fluid inclusion and oxygen and hydrogen isotope studies to determine the nature and origin of the hydrothermal fluids that generated the deposit. The temperature of the ore‐forming fluid shows a range of 86 to 302 °C. Our detailed microthermometric data show that the temperature during mineralization of the fluorite and barite in the early ore‐forming stage was higher than that during the formation of the calcite in the late ore‐forming stage. The salinity varied substantially from 0.18% to 21.19% NaCl eqv., whereas the density was around 1.00 g/cm3. The fluid composition was mainly H2O (>91.33%), followed by CO2, CH4 and traces of C2H6, CO, Ar, and H2S. The dominant cation was Na+ and the dominant anion Cl‐, followed by Ca2+, SO42‐, K+, and Mg2+, indicating a mid–low‐temperature, mid‐low‐salinity, low‐density NaCl–H2O system. Our results demonstrate that the temperature decreased during the ore‐forming process and the fluid system changed from a closed reducing environment to an open oxidizing environment. The hydrogen and oxygen isotope data demonstrate that the hydrothermal fluids in the study area had multiple sources, primarily formation water, as well as meteoric water and metamorphic water. Combined with the geological setting and mineralization features we infer that the stratabound barite–fluorite deposits originated from mid–low‐temperature hydrothermal fluids and formed vein filling in the fault zone. 相似文献