Japan Geoscience Union Meeting 2016

Presentation information


Symbol B (Biogeosciences) » B-PT Paleontology

[B-PT05] Decoding the history of Earth: From Hadean to Modern

Wed. May 25, 2016 3:30 PM - 5:00 PM 105 (1F)

Convener:*Tsuyoshi Komiya(Department of Earth Science & Astronomy Graduate School of Arts and Sciences The University of Tokyo), Yasuhiro Kato(Department of Systems Innovation, Graduate School of Engineering, University of Tokyo), Katsuhiko Suzuki(Research and Development Center for Submarine Resources, Japan Agency for Marine-Earth Science and Technology), Chair:Shogo Aoki(Graduate School of arts and science, University of Tokyo)

3:45 PM - 4:00 PM

[BPT05-20] Authigenic carbonate precipitation at the end-Guadalupian (Middle Permian) in China: Implications for the carbon cycle in ancient anoxic oceans

*Masafumi Saitoh1, Yuichiro Ueno2, Yukio Isozaki3, Takazo Shibuya1, Katsumi Shozugawa3, Motoyuki Matsuo3, Naohiro Yoshida2 (1.JAMSTEC, 2.Tokyo Tech, 3.Univ Tokyo)

Carbonate precipitation is a major process in the global carbon cycle. It was recently proposed that authigenic carbonate (carbonate precipitated in situ at the sediment–water interface and/or within the sediment) played a major role in the carbon cycle throughout Earth’s history. The carbon isotopic composition of authigenic carbonates in ancient oceans have been assumed to be significantly lower than that of dissolved inorganic carbon (DIC) in seawater, as is observed in the modern oceans. However, the d13C values of authigenic carbonates in the past has not been analyzed in detail. Here, we report authigenic carbonates in the uppermost Guadalupian (Middle Permian) rocks at Chaotian, Sichuan, South China. Monocrystalline calcite crystals <20 mm long are common in the black mudstone/chert sequence that was deposited on a relatively deep anoxic slope/basin along the continental margin. Textures of the crystals indicate in situ precipitation on the seafloor and/or within the sediments. The calcite precipitation corresponds stratigraphically with denitrification and sulfate reduction in the anoxic deep-water mass, as indicated by previously reported nitrogen and sulfur isotope records, respectively. Relatively high d13C values of the authigenic carbonates (largely -1‰) compared with those of organic matter in the rocks (ca. -26‰) suggest that the main carbon source of the carbonates was DIC in the water column. The calcite crystals precipitated in an open system with respect to carbonate, possibly near the sediment–water interface rather than deep within the sediments. The d13C values of the carbonates were close to the d13C value of seawater due to mixing of 13C-depleted remineralized organic carbon (that was released into the water column by the water-mass anaerobic respiration) with the large DIC pool in the oceans. Our results imply that d13C values of authigenic carbonates in the anoxic oceans might have been systematically different from the values in the oxic oceans in Earth’s history, controlled by the depth of the redoxcline in the water column and sediments. If our model is correct, authigenic carbonates with relatively high d13C values in the ancient anoxic oceans may have had a less substantial influence on the bulk d13C values in geologic records than has been previously suggested.
[ref.] Saitoh et al. (2015) Progress in Earth and Science 2:41