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131.
Yasunori Mahara Tomoko Ohta Tomochika Tokunaga Hiroyuki Matsuzaki Eiji Nakata Yuki Miyamoto Yukihiro Mizuochi Toshiharu Tashiro Masahiro Ono Toshifumi Igarashi Keisuke Nagao 《Applied Geochemistry》2012
Fifty-three samples, including brines associated with oil and natural gas reservoirs and groundwater samples from deep boreholes, were collected from the Pacific and Japan Sea coastal regions in Japan. The 129I/127I and 36Cl/Cl ratios, and stable isotopes (δD and δ18O) are compared to investigate differences related to the geotectonic settings of the two regions. The δD and δ18O data indicate that brine and groundwater from the Pacific coastal region reflect mixing of meteoric water with connate seawater in the pores of sedimentary rocks. On the other hand, brine and groundwater from the Japan Sea coastal region have been hydrothermally altered. In particular, brines associated with petroleum accumulations at Niigata and Akita showed the same isotopic characteristics as fluids found in the Kuroko deposits of the Green Tuff region in northeastern Japan. There is little difference in the 36Cl/Cl ratios in brine and groundwater from the Pacific and Japan Sea coasts. Most brine and some deep groundwater, except those from the Pleistocene Kazusa Group, have already reached the average secular equilibrium ratio of 9.9 ± 2.7 × 10−15 for their mudstone and sandstone reservoirs. There was no correlation between the 36Cl/Cl ratios and differences in geotectonic setting between the Pacific and the Japan Sea coast. The molar I/Br ratio suggests that the I in all of water samples was of biogenic origin. The average 129I/127I ratio was 290 ± 130 × 10−15 to 294 ± 105 × 10−15 in both regions, showing no relationship to the different geotectonic settings. The uncontaminated brine and groundwater samples are likely to have retained the original 129I/127I ratios of marine I released from the old organic matter stored in sedimentary rock. 相似文献
132.
Takashi Tomiyasu Akito Matsuyama Ryusuke Imura Hitoshi Kodamatani Junko Miyamoto Yuriko Kono David Kocman Jo?e Kotnik Vesna Fajon Milena Horvat 《Environmental Earth Sciences》2012,65(4):1309-1322
Although the mining activity of the Idrija mine in Slovenia ceased in 1995, a large amount of mining dregs containing high
concentrations of mercury remains in the area. The mining dregs were transported with river flow and deposition along the
Idrija River. To estimate the dispersion and change in the chemical form of mercury, a total of 28 soil core samples were
taken around the river. The individual core samples were separated into layers for the analysis of their chemical composition,
carbon contents, total mercury (T-Hg) and methylmercury (MeHg) concentrations. The chemical composition measured by X-ray
fluorescence spectrometry was useful to estimate the dispersion of tailings: the fluvial terrace soil had a chemical composition
similar to that of the tailings and could be distinguished clearly from the forest soil. The highest T-Hg concentration, 1,100 mg kg−1, was observed in the fluvial terrace soil near the mine. Although the concentration decreased gradually along with distance
from the mine, concentrations higher than 200 mg kg−1 of T-Hg were still observed in the fluvial terrace soil approximately 20 km downstream from the mine. In the vertical distribution
of T-Hg in the hillslope soil, a higher value was observed in the upper layers, which suggests the recent atmospheric deposition
of mercury. The concentration of MeHg was the lowest at the riverside and higher in the hillslope soil, which was the opposite
of the T-Hg distribution. The total organic carbon content tracked similarly with the distribution of MeHg and a linear relation
with a significantly high correlation coefficient was obtained. The distinction may be related to the different dispersion
process of mercury, and the organic carbon contents may be an important factor for MeHg formation. 相似文献
133.
Ando Haruo Maki Hideaki Kashiwagi Nobuhisa Ishii Yuuichi 《Journal of Oceanography》2021,77(6):843-858
Journal of Oceanography - Long-term trends of bottom-water concentrations of dissolved oxygen (DO), total nitrogen, and total phosphorus at 42 sites in Tokyo Bay were analyzed using monthly data... 相似文献
134.
Granulite grade marble layers interlayered with metapelitic granulites from Lützow Holm Bay, East Antarctica, provide insight into fluid–rock interactions during burial to and exhumation from lower crustal levels. Sub-millimeter scale strontium, oxygen and carbon isotope variations along with LA-ICPMS trace element geochemistry and mineral chemistry of texturally characterized carbonates and associated minerals helped to reconstruct the multistage metamorphic fluid history.Fluid–rock interaction dating back to prograde metamorphism are still preserved in consistently low oxygen and high strontium isotope compositions (δ18O = 12‰; 87Sr/86Sr(550Ma) = 0.7248) within a massif dolomitic marble layer that escaped significant later metasomatism. In most marbles, total re-crystallization and isotopic resetting occurred in the presence of “externally derived” hyper-saline fluids that circulated along the carbonate layers during the early stages of prograde metamorphism. This leads to a trend of increased radiogenic Sr in marbles towards the value of associated metapelitic rocks that have 87Sr/86Sr(550Ma) of 0.764.LA-ICPMS studies on trace elements in carbonate and associated silicate minerals at different textural settings, distinguished using cathodoluminescence microscopy, revealed multiple metasomatic events during retrograde metamorphism. Trace element contents of Ba, Sr, Pb and U gave compelling evidence for metasomatic alteration that postdate the exsolution of carbonate at ~ 600 ºC, which can be correlated with the fluids released from the crystallization of anatectic melts and pegmatites. Subsequently, meteoric fluid infiltration occurred at a shallower level of the crust and caused extreme oxygen isotopic heterogeneity (δ18O = 14.7 ~ ? 4.9‰) and imprinted high concentration of fluid mobile elements. Taken together our results emphasize the importance of integrating textural and chemical heterogeneities to reveal the multiple episodes of fluid–rock interaction processes in a dynamic continental crust, which has major implications on migration of fluids and material and help in formulating models on the geodynamic evolution of crust. 相似文献
135.
Antarctic lunar meteorites Yamato-793169, Asuka-881757, MIL 05035, and MET 01210 (YAMM): Launch pairing and possible cryptomare origin 总被引:1,自引:0,他引:1
Tomoko Arai B. Ray Hawke Keiji Misawa Masamichi Miyamoto 《Geochimica et cosmochimica acta》2010,74(7):2231-3852
The Antarctic lunar meteorite Meteorite Hills (MET) 01210 is a polymict regolith breccia, dominantly composed of mare basalt components. One relatively large (2.7 × 4.7 mm) basalt clast in MET 01210 (MET basalt) shows remarkable mineralogical similarities to the lunar-meteorite crystalline mare basalts Yamato (Y)-793169, Asuka (A)-881757, and Miller Range (MIL) 05035. All four basalts have similar rock texture, mineral assemblage, mineral composition, pyroxene crystallization trend, and pyroxene exsolution lamellae. The estimated TiO2 contents (∼2.0 wt%) of the MET basalt and MIL 05035 are close to the bulk-rock TiO2 contents of Y-793169 and A-881757. These similarities suggest that Y-793169, A-881757, MIL 05035, and the MET basalt came from the same basalt flow, which we designate the YAMM basalt. The source-basalt pairing of the YAMM is also supported by their similar REE abundances, crystallization ages (approx. 3.8-3.9 Ga), and isotopic compositions (low U/Pb, low Rb/Sr, and high Sm/Nd). The pyroxene exsolution lamellae, which are unusually coarse (up to a few microns) by mare standards, imply a relatively slow cooling in an unusually thick lava and/or subsequent annealing within a cryptomare. Reported noble gas and CRE data with close launch ages (∼1 Ma) and ejection depths (deeper than several meters) among the four meteorites further indicate their simultaneous ejection from the moon. Despite the marginally close terrestrial ages, pairing in the conventional Earth-entry sense seems unlikely because of the remote recovery sites among the YAMM meteorites.The high abundance (68%) of mare components in MET 01210 estimated from a two-component mixing model calculation could have resulted from either lateral mixing at a mare-highland boundary or vertical mixing in a cryptomare. The proportion of mare materials in MET 01210 is greater than in Apollo core samples at the mare-highland boundary. The burial depth (>several meters deep) inferred from the lack of surface irradiation of MET 01210 exceeds the typical mare regolith thickness (a few meters). Thus, the source of the YAMM meteorites is likely a terrain of locally high mare-highland mixing within a cryptomare. We searched for a possible source crater of the YAMM meteorites within the well-defined cryptomare, based on the multiple constraints obtained from this study and published data. An unnamed 1.4 km-diameter crater (53°W, 44.5°S) on the floor of the Schickard crater is the most suitable source for the YAMM meteorites.The 238U/204Pb (μ) value of the YAMM basalts is extremely low, relative to those of the Apollo mare basalts, but comparable to those of the Luna 24 very low-Ti basalts. The low-μ source indicates a derivation from a less differentiated mantle with a lack of KREEP components. Although the chemical sources of materials and heat source of melting might be independent, the heat source that generated the source magma of the YAMM and Luna 24 basalts may not be related to KREEP, unlike the case of the Apollo basalts. The distinct chemical and isotopic compositions of mantle sources between the Apollo basalts and the YAMM/Lunar 24 basalts imply differences in mantle composition and thermal evolution between the Procellarum KREEP Terrane (PKT) and non-PKT regions of the nearside. 相似文献
136.
We measured molecular distributions and compound-specific hydrogen (δD) and stable carbon isotopic ratios (δ13C) of mid- and long-chain n-alkanes in forest soils, wetland peats and lake sediments within the Dorokawa watershed, Hokkaido, Japan, to better understand sources and processes associate with delivery of terrestrial organic matter into the lake sediments. δ13C values of odd carbon numbered C23-C33n-alkanes ranged from −37.2‰ to −31.5‰, while δD values of these alkanes showed a large degree of variability that ranged from −244‰ to −180‰. Molecular distributions in combination with stable carbon isotopic compositions indicate a large contribution of C3 trees as the main source of n-alkanes in forested soils whereas n-alkanes in wetland soil are exclusively derived from marsh grass and/or moss. We found that the n-alkane δD values are much higher in forest soils than wetland peat. The higher δD values in forest samples could be explained by the enrichment of deuterium in leaf and soil waters due to increased evapotranspiration in the forest or differences in physiology of source plants between wetland and forest. A δ13C vs. δD diagram of n-alkanes among forest, wetland and lake samples showed that C25-C31n-alkanes deposited in lake sediments are mainly derived from tree leaves due to the preferential transport of the forest soil organic matter over the wetland or an increased contribution of atmospheric input of tree leaf wax in the offshore sites. This study demonstrates that compound-specific δD analysis provides a useful approach for better understanding source and transport of terrestrial biomarkers in a C3 plant-dominated catchment. 相似文献