Micro-scale CO2 and CH4 dynamics in a peat soil during a water fluctuation and sulfate pulse

被引:75
作者
Blodau, C
Moore, TR
机构
[1] McGill Univ, Dept Geog, Montreal, PQ H3A 2K6, Canada
[2] McGill Univ, Ctr Climate & Global Change Res, Montreal, PQ H3A 2K6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
peatlands; carbon dioxide; methane; sulfate; pore water;
D O I
10.1016/S0038-0717(03)00008-7
中图分类号
S15 [土壤学];
学科分类号
0903 ; 090301 ;
摘要
We investigated the response Of CO2 and CH4 production to a water table fluctuation and a SO42- pulse in a bog mesocosm. Net gas production rates in the mesocosm were calculated from concentration data by diffusive mass-balances. Incubation experiments were used to quantify the effect of SO42- addition and the distribution of potential CO2 and CH4 production rates. Flooding of unsaturated peat resulted in rapid depletion of O-2 and complex patterns of net CH4, CO2, and H2S production. Methane production began locally and without a time lag at rates of 3-4 nmol cm(-3) d(-1) deeper in the peat. Similar rates were determined after a time lag of 10-60 days in the surface layers, whereas rates at lower depths declined. Net CO2 production was largest immediately after the water table position was altered (100-300 nmol cm(-3) d(-1)) and declined to -50-50 nmol cm(-3) d(-1) after a few weeks. SO42- addition (500 mM) significantly increased potential CH4 production rates in the surface layer from an average of 132-201 nmol cm(-3) d(-1) and reduced it below from an average of 418-256 nmol cm(-3) d(-1). Our results suggest that deeper in the peat (40-70 cm) under in situ conditions, methanogenic populations are less impaired by unsaturated conditions than in the surface layers, and that at these depths after flooding the substrate availability for CH4 and DIC production is significantly enhanced. They also suggest that methanogenic and SO42--reducing activity were non-competitive in the surface layer, which might explain contradictory findings from field studies. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:535 / 547
页数:13
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