کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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2027081 | 1070085 | 2006 | 9 صفحه PDF | دانلود رایگان |
Stable 15N isotope dilution and tracer techniques were used in cultivated (C) and uncultivated (U) ephemeral wetlands in central Saskatchewan, Canada to: (1) quantify gross mineralization and nitrification rates and (2) estimate the relative proportion of N2O emissions from these wetlands that could be attributed to denitrification versus nitrification-related processes. In-field incubation experiments were repeated in early May, mid-June and late July. Mean gross mineralization and nitrification rates (10.3 and 3.1 mg kg−1 d−1, respectively) did not differ between C and U wetlands on any given date. Despite these similarities, the mean NH4+ pool size in the U wetlands (17.2 mg kg−1) was two to three times that of the C wetlands (6.7 mg kg−1) whereas the mean NO3− pool size in U wetlands (2.2 mg kg−1) was less than half that of C wetlands (5.8 mg kg−1). Mean N2O emissions from the C wetlands decreased from 112.8 to 17.0 ng N2O m2 s−1 from May to July, whereas mean U-wetland N2O emissions ranged only from 31.8 to 51.1 ng N2O m2 s−1 over the same period. This trend is correlated to water-filled pore space in C wetlands, demonstrating a soil moisture influence on emissions. Denitrification is generally considered the dominant emitter of N2O under anaerobic conditions, but in the C wetlands, only 49% of the May emissions could be directly attributed to denitrification, decreasing to 29% in July. In contrast, more than 75% of the N2O emissions from the U wetlands arose from denitrification of the soil NO3− pool throughout the season. These land use differences in emission sources and rates should be taken into consideration when planning management strategies for greenhouse gas mitigation.
Journal: Soil Biology and Biochemistry - Volume 38, Issue 12, December 2006, Pages 3398–3406