Biogeochemistry and biodiversity of methane cycling in subsurface marine sediments (Skagerrak, Denmark)

RJ Parkes, BA Cragg, N Banning… - Environmental …, 2007 - Wiley Online Library
RJ Parkes, BA Cragg, N Banning, F Brock, G Webster, JC Fry, E Hornibrook, RD Pancost
Environmental Microbiology, 2007Wiley Online Library
This biogeochemical, molecular genetic and lipid biomarker study of sediments (∼ 4 m
cores) from the Skagerrak (Denmark) investigated methane cycling in a sediment with a
clear sulfate‐methane‐transition zone (SMTZ) and where CH4 supply was by diffusion,
rather than by advection, as in more commonly studied seep sites. Sulfate reduction
removed sulfate by 0.7 m and CH4 accumulated below. 14C‐radiotracer measurements
demonstrated active H2/CO2 and acetate methanogenesis and anaerobic oxidation of CH4 …
Summary
This biogeochemical, molecular genetic and lipid biomarker study of sediments (∼4 m cores) from the Skagerrak (Denmark) investigated methane cycling in a sediment with a clear sulfate‐methane‐transition zone (SMTZ) and where CH4 supply was by diffusion, rather than by advection, as in more commonly studied seep sites. Sulfate reduction removed sulfate by 0.7 m and CH4 accumulated below. 14C‐radiotracer measurements demonstrated active H2/CO2 and acetate methanogenesis and anaerobic oxidation of CH4 (AOM). Maximum AOM rates occurred near the SMTZ (∼3 nmol cm−3 day−1 at 0.75 m) but also continued deeper, overall, at much lower rates. Maximum rates of H2/CO2 and acetate methanogenesis occurred below the SMTZ but H2/CO2 methanogenesis rates were × 10 those of acetate methanogenesis, and this was consistent with initial values of 13C‐depleted CH413C c.−80‰). Areal AOM and methanogenic rates were similar (∼1.7 mmol m−2 day−1), hence, CH4 flux is finely balanced. A 16S rRNA gene library from 1.39 m combined with methanogen (T‐RFLP), bacterial (16S rRNA DGGE) and lipid biomarker depth profiles showed the presence of populations similar to some seep sites: ANME‐2a (dominant), ANME‐3, Methanomicrobiales, Methanosaeta Archaea, with abundance changes with depth corresponding to changes in activities and sulfate‐reducing bacteria (SRB). Below the SMTZ to ∼1.7 m CH4 became progressively more 13C depleted (δ13C −82‰) indicating a zone of CH4 recycling which was consistent with the presence of 13C‐depleted archaeol (δ13C −55‰). Pore water acetate concentrations decreased in this zone (to ∼5 μM), suggesting that H2, not acetate, was an important CH4 cycling intermediate. The potential biomarkers for AOM‐associated SRB, non‐isoprenoidal ether lipids, increased below the SMTZ but this distribution reflected 16S rRNA gene sequences for JS1 and OP8 bacteria rather than those of SRB. At this site peak rates of methane production and consumption are spatially separated and seem to be conducted by different archaeal groups. Also AOM is predominantly coupled to sulfate reduction, unlike recent reports from some seep and gassy sediment sites.
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Bibliography

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