Abstract:We conducted headspace gas analyses using cores from two 520 m boreholes to evaluate the gas permeability of Neogene sedimentary rocks in Horonobe, Hokkaido, Japan. Analytical data suggest that most hydrocarbon gases are microbial methane. Further analyses of these data indicated that the low concentration and heavy carbon isotope composition of methane could be explained by carbon isotopic fractionation during migration near fractures. The high residual volume of microbial methane observed in the study area s… Show more
“…Funaki et al . [] reported that the δ 13 C CH4 and C 1 /(C 2 + C 3 ) ratios of a biogenic gas from Neogene sedimentary rocks in the Horonobe area are less than −50‰ and several thousand, respectively.…”
Section: Discussionmentioning
confidence: 99%
“…The d 13 C CH4 and C 1 /(C 2 1 C 3 ) ratios of the gas in the Haboro and Hakobuchi formations, as determined by head-space analysis, are approximately 230& and <10, respectively [JNOC, 1995]; these values indicate that the gases are of thermogenic origin [JNOC, 1995]. Funaki et al [2012] reported that the d 13 C CH4 and C 1 /(C 2 1 C 3 ) ratios of a biogenic gas from Neogene sedimentary rocks in the Horonobe area are less than 250& and several thousand, respectively.…”
[1] The origin of muddy sand and gas in muddy sand sediments in the Horonobe area of northern Hokkaido, Japan, was investigated by analyzing the mineralogical and chemical compositions of the sediments and the chemical/isotopic compositions of the gas. X-ray fluorescence and X-ray diffraction analyses indicate that chemically, the muddy sand is derived from a mixing of components from the Hakobuchi and overlying formations, and that the characteristic mineral of the muddy sand is heulandite, which, in the study area, has been detected only in the Hakobuchi Formation. These results suggest that the sediments ascended from depths of at least 2200-2400 m. The d 13 C CH4 values and the methane/ (ethane 1 propane) ratios of the gas indicate that the primary origin of the methane is by thermogenic decomposition of coal-bearing beds in the Haboro or Hakobuchi formations, or further deep sources. This study provides new data on processes of onshore mud volcanism in Japan, and contributes to an understanding of processes of subsurface mass transport in regions of mud-volcanic activity.
“…Funaki et al . [] reported that the δ 13 C CH4 and C 1 /(C 2 + C 3 ) ratios of a biogenic gas from Neogene sedimentary rocks in the Horonobe area are less than −50‰ and several thousand, respectively.…”
Section: Discussionmentioning
confidence: 99%
“…The d 13 C CH4 and C 1 /(C 2 1 C 3 ) ratios of the gas in the Haboro and Hakobuchi formations, as determined by head-space analysis, are approximately 230& and <10, respectively [JNOC, 1995]; these values indicate that the gases are of thermogenic origin [JNOC, 1995]. Funaki et al [2012] reported that the d 13 C CH4 and C 1 /(C 2 1 C 3 ) ratios of a biogenic gas from Neogene sedimentary rocks in the Horonobe area are less than 250& and several thousand, respectively.…”
[1] The origin of muddy sand and gas in muddy sand sediments in the Horonobe area of northern Hokkaido, Japan, was investigated by analyzing the mineralogical and chemical compositions of the sediments and the chemical/isotopic compositions of the gas. X-ray fluorescence and X-ray diffraction analyses indicate that chemically, the muddy sand is derived from a mixing of components from the Hakobuchi and overlying formations, and that the characteristic mineral of the muddy sand is heulandite, which, in the study area, has been detected only in the Hakobuchi Formation. These results suggest that the sediments ascended from depths of at least 2200-2400 m. The d 13 C CH4 values and the methane/ (ethane 1 propane) ratios of the gas indicate that the primary origin of the methane is by thermogenic decomposition of coal-bearing beds in the Haboro or Hakobuchi formations, or further deep sources. This study provides new data on processes of onshore mud volcanism in Japan, and contributes to an understanding of processes of subsurface mass transport in regions of mud-volcanic activity.
“…The δ 13 C CH4 values of gases from depths of <1000 m, in the biogenic region, are usually in the range of -70‰ to −60‰, with isotopic compositions becoming heavier as depth increases towards the thermogenic region (e.g., [12,13]). Large variations in carbon isotopic ratios in CH 4 and CO 2 are often reported for depths of <1000 m, with δ 13 C CH4 values sometimes reaching −20‰ (e.g., [14][15][16][17]). These variations are associated with the effects of microbial activity on methane production or oxidation in underground environments [18].…”
Section: Introductionmentioning
confidence: 99%
“…In a previous study, gas samples from two boreholes (PB-V01 and SAB-1, both~500 m deep) in the Horonobe area, Hokkaido, were processed using IsoJar™ containers [14]. In that study, cores were stored in IsoJar™ containers with water and a few drops of BKC solution [14] for up to three months before headspace analysis.…”
Section: Introductionmentioning
confidence: 99%
“…In a previous study, gas samples from two boreholes (PB-V01 and SAB-1, both~500 m deep) in the Horonobe area, Hokkaido, were processed using IsoJar™ containers [14]. In that study, cores were stored in IsoJar™ containers with water and a few drops of BKC solution [14] for up to three months before headspace analysis. Because sampling date of cores and analysis date of gases, which are necessary for the calculation of the storage period, have not been presented in Funaki et al [14], these unpublished information are summarized in Tables S1a and S1b.…”
The IsoJar™ container is widely used in headspace gas analysis for gases adsorbed on cuttings or bore cores from oil and gas fields. However, large variations in the carbon isotopic ratios of CH4 and CO2 are often reported, especially for data obtained from depths of <1000 m. The IsoJar™ method leaves air in the headspace that allows microbial oxidation of CH4 to CO2, meaning that isotopic fractionation occurs during storage. This study employed the IsoJar™ method to investigate the causes of differences in δ13C data reported by previous studies in the Horonobe area of Japan. It was found that after 80 d storage, δ13CCO2 values decreased by ~2‰, while δ13CCH4 values increased by >30‰, whereas samples analyzed within a week of collection showed no such fluctuations. The conventional amount of microbial suppressant (~0.5 ml of 10% benzalkonium chloride (BKC) solution) is insufficient to suppress microbial activity if groundwater is used as filling water. The significant variations in carbon isotopic compositions previously reported were caused by microbial methane oxidation after sampling and contamination by groundwater from different depths. To avoid these problems, we recommend the following: (1) if long-term sample storage is necessary, >10 ml of 10% BKC solution should be added or >0.3% BKC concentration is required to suppress microbial activity; (2) analyses should be performed within one week of sampling; and (3) for CO2 analyses, it is important that samples are not contaminated by groundwater from different depths.
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