LONG-TERM EFFECTS OF NITROGEN-FERTILIZATION ON METHANE OXIDATION IN SOIL OF THE BROADBALK WHEAT EXPERIMENT

Citation
Bw. Hutsch et al., LONG-TERM EFFECTS OF NITROGEN-FERTILIZATION ON METHANE OXIDATION IN SOIL OF THE BROADBALK WHEAT EXPERIMENT, Soil biology & biochemistry, 25(10), 1993, pp. 1307-1315
Citations number
34
Categorie Soggetti
Agriculture Soil Science
Journal title
ISSN journal
00380717
Volume
25
Issue
10
Year of publication
1993
Pages
1307 - 1315
Database
ISI
SICI code
0038-0717(1993)25:10<1307:LEONOM>2.0.ZU;2-Z
Abstract
Methane uptake by a temperate arable soil was investigated in incubati on experiments with intact soil cores. The measurements were carried o ut with a soil moisture content of 16-17% (w/w) and at 25-degrees-C. T he decrease of the CH4 concentrations in an amended atmosphere (10 mul CH4 l-1) was measured during a 212 h period. There was no decrease of CH4 if the soil was autoclaved showing that the disappearance of meth ane was entirely mediated by microbial activity. The long-term applica tion (140 yr) of mineral nitrogen fertilizer caused significant differ ences in the ability of the soil to oxidize CH4: the larger the amount of fertilizer applied the lower the rate of CH4 oxidation. No signifi cant short-term effect of mineral-N fertilization could be observed wh ether applied as (NH4)2SO4 or KNO3. An organic manure treatment, which has received nearly 240 kg N ha-1 each year as farmyard manure, showe d almost the same ability to oxidize CH4 as an unfertilized plot and h ad a significantly higher CH, oxidation rate after an application of 1 44 kg N ha-1 as nitrate fertilizer. For the mineral-N treatments the i nhibition of the CH4 oxidation increased with increasing N turnover ra te but was independent of the mineral nitrogen content of the soil at the time of measurement Therefore, the continued application of minera l-N fertilizer for an extended period (at least 7 yr) caused a depleti on of the bacterial methane sink in soil and may have contributed to t he continuous increase in atmospheric CH4 over the past decades.