The 3He/4He and 4He/20Ne ratios of 115 natural gas samples, including various types of gases from volcanoes, hot springs, mineral springs, water wells, petroleum fields, and natural gas fields, were measured using a mass spectrometer. The observed 3He/4He and 4He/20Ne ratios range from 7.47×10−8 to 9.65×10 −6 and from 0.26 to 1100, respectively. The 3He/4He ratios reflect well the geotectonic structure of the Japanese Islands. In northeastern (NE) Japan there is a clear geographical difference in the 3He/4He ratios between the frontal arc (forearc) and volcanic arc (back arc) regions. Lower ratios were found in the trench side region and higher ratios in the back arc side. This result suggests that the mantle‐derived helium in the volcanic arc region is associated with the diapiric uprise of a magma. Lower 3He/4He ratios in the frontal arc region may be due to radiogenic He produced by radioactive decay of U and Th in the crustal and sedimentary rocks. In southwestern (SW) Japan there is no clear geographical contrast in the 3He/4He ratios. Some samples in the frontal arc region show quite high 3He/4He ratios. The tendency of the 3He/4He ratios agrees with the distribution of terrestrial heat flow data and reflects geotectonic structures different from NE Japan. The high 3He/4He ratios observed in the frontal arc region in SW Japan may be indicative of renewed or incipient magmatism due to a descending young and warm slab.
Carbon dioxide-rich fluid bubbles, containing approximately 86 percent CO(2), 3 percent H(2)S, and 11 percent residual gas (CH(4) + H(2)), were observed to emerge from the sea floor at 1335- to 1550-m depth in the JADE hydrothermal field, mid-Okinawa Trough. Upon contact with seawater at 3.8 degrees C, gas hydrate immediately formed on the surface of the bubbles and these hydrates coalesced to form pipes standing on the sediments. Chemical composition and carbon, sulfur, and helium isotopic ratios indicate that the CO(2)-rich fluid was derived from the same magmatic source as dissolved gases in 320 degrees C hydrothermal solution emitted from a nearby black smoker chimney. The CO(2)-rich fluid phase may be separated by subsurface boiling of hydrothermal solutions or by leaching of CO(2)-rich fluid inclusion during posteruption interaction between pore water and volcanogenic sediments.
Chloride (Cl(-)) and sulfate (SO(4)(2-)) ion concentrations of ground water issuing from two wells located near the epicenter of the Kobe earthquake in Japan fluctuated before the disastrous magnitude 7.2 event on 17 January 1995. The samples measured were pumped ground water packed in bottles and distributed in the domestic market as drinking water from 1993 to April 1995. Analytical results demonstrate that Cl(-)and SO(4)(2-) concentrations increased steadily from August 1994 to just before the earthquake. Water sampled after the earthquake showed much higher Cl(-) and SO(4)(2-) concentrations. The precursory changes in chemical composition may reflect the preparation stage of a large earthquake.
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