Abstract
GEOCHEMISTRY GEOPHYSICS GEOSYSTEMS,
VOL. 9,
Q04N14,
26 PP., 2008
doi:10.1029/2006GC001558 [Citation]
Radiocarbon-based carbon source quantification of anomalous isotopic foraminifera in last glacial sediments in the western North Pacific
AMS Facility (NIES-TERRA), Environmental Chemistry Division, National Institute for Environmental Studies (NIES), Tsukuba 305-8506, Japan
Institute of Oceanographic Research for Global Changes (IORGC), Japan Agency for Marine-Earth Science and Technology (JAMSTEC), Yokosuka 237-0061, Japan
Geological Survey of Japan, National Institute of Advanced Industrial Science and Technology (AIST), 1-1-1, Higashi, Tsukuba 305-8567, Japan
Institute of Oceanographic Research for Global Changes (IORGC), Japan Agency for Marine-Earth Science and Technology (JAMSTEC), Yokosuka 237-0061, Japan
Kochi Institute for Core Sample Research, Japan Agency for Marine-Earth Science and Technology (JAMSTEC), Nankoku, Kochi 783-8502, Japan
Earth and Planetary System Science, Faculty of Science, Hokkaido University, Sapporo 060-0810, Japan
Earth and Planetary System Science, Faculty of Science, Hokkaido University, Sapporo 060-0810, Japan
Geological Survey of Japan, National Institute of Advanced Industrial Science and Technology (AIST), 1-1-1, Higashi, Tsukuba 305-8567, Japan
AMS Facility (NIES-TERRA), Environmental Chemistry Division, National Institute for Environmental Studies (NIES), Tsukuba 305-8506, Japan
A previous study interpreted extremely 13C-depleted excursions of planktonic and benthic foraminifera in last glacial sediments (17,500 to 25,400 cal years B.P.) of the core retrieved from off Shimokita Peninsula and off Hokkaido, Japan, as evidence for periodic releases of methane, arising from the dissociation of methane hydrate. To better understand the formation process of the 13C-depleted excursions, we conducted high-resolution natural radiocarbon measurements and biogeochemical analyses. We found highly depleted 13C excursions ranging from −10.2‰ to −1.6‰ and −6.8‰ to −1.6‰ in planktonic and benthic foraminifera, respectively. Most of the foraminiferal tests in these horizons were brown, most likely as a result of postdepositional alteration, reflecting the formation of authigenic carbonate on the surface of tests. These alterations were also supported by high levels of Mg-calcite and the acid-leaching test for anomalous foraminifera. To evaluate the carbon sources in the altered foraminifera tests, we quantified the relative contributions of 14C-free methane-derived carbon sources to the formation of authigenic carbonates in foraminifera with depleted 13C excursions using a coupled mass balance isotopic model (14C/C and 13C/12C). The radiocarbon ages of both planktonic and benthic 13C-depleted foraminifera were approximately 600 to 2000 years older than those of normal tests from nearby horizons. The relative contributions of authigenic carbonates derived from the methane oxidizing process reached to ∼22 wt% for planktonic foraminifera and ∼15 wt% for benthic foraminifera. The δ 13C values of methane calculated from the mass balance model were between −29‰ and −68‰ for planktonic foraminifera and between −40‰ and −108‰ for benthic foraminifera, consistent with δ 13C values reported for thermogenic and abiogenic methane in global methane hydrate reservoirs. These data consistently suggest that methane-related drastic environmental change occurred in the horizons that included δ 13C anomalies. This study provides important information for interpreting geological records of the methane hydrate instability associated with climate.
Received 16 December 2006; accepted 25 December 2007; published 2 April 2008.
Citation: (2008), Radiocarbon-based carbon source quantification of anomalous isotopic foraminifera in last glacial sediments in the western North Pacific, Geochem. Geophys. Geosyst., 9, Q04N14, doi:10.1029/2006GC001558.
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