Heiner Flessa

Terrestrial ecosystems in northern high latitudes exchange large amounts of methane (CH₄) with the atmosphere. Climate warming could have a great impact on CH₄ exchange, in particular in regions where degradation of permafrost is induced. In order to improve the understanding of the present and future methane dynamics in permafrost regions, we studied CH₄ fluxes of typical landscape structures in a small catchment in the forest tundra ecotone in northern Siberia. Gas fluxes were measured using a closed‐chamber technique from August to November 2003 and from August 2006 to July 2007 on tree‐covered mineral soils with and without permafrost, on a frozen bog plateau, and on a thermokarst pond. For areal integration of the CH₄ fluxes, we combined field observations and classification of functional landscape structures based on a high‐resolution Quickbird satellite image. All mineral soils were net sinks of atmospheric CH₄. The magnitude of annual CH₄ uptake was higher for soils without permafrost (1.19 kg CH₄ ha⁻¹ yr⁻¹) than for soils with permafrost (0.37 kg CH₄ ha⁻¹ yr⁻¹). In well‐drained soils, significant CH₄ uptake occurred even after the onset of ground frost. Bog plateaux, which stored large amounts of frozen organic carbon, were also a net sink of atmospheric CH₄ (0.38 kg CH₄ ha⁻¹ yr⁻¹). Thermokarst ponds, which developed from permafrost collapse in bog plateaux, were hot spots of CH₄ emission (approximately 200 kg CH₄ ha⁻¹ yr⁻¹). Despite the low area coverage of thermokarst ponds (only 2.1% of the total catchment area), emissions from these sites resulted in a mean catchment CH₄ emission of 3.8 kg CH₄ ha⁻¹ yr⁻¹. Export of dissolved CH₄ with stream water was insignificant. The results suggest that mineral soils and bog plateaux in this region will respond differently to increasing temperatures and associated permafrost degradation. Net uptake of atmospheric CH₄ in mineral soils is expected to gradually increase with increasing active layer depth and soil drainage. Changes in bog plateaux will probably be much more rapid and drastic. Permafrost collapse in frozen bog plateaux would result in high CH₄ emissions that act as positive feedback to climate warming.

Quantitative information about the amount and stability of organic carbon (OC) in different soil organic‐matter (OM) fractions and in specific organic compounds and compound‐classes is needed to improve our understanding of organic‐matter sequestration in soils. In the present paper, we summarize and integrate results performed on two different arable soils with continuous maize cropping (a) Stagnic Luvisol with maize cropping for 24 y, b) Luvic Phaeozem with maize cropping for 39 y) to identify (1) the storage of OC in different soil organic‐matter fractions, (2) the function of these fractions with respect to soil‐OC stabilization, (3) the importance and partitioning of fossil‐C deposits, and (4) the rates of soil‐OC stabilization as assessed by compound‐specific isotope analyses. The fractionation procedures included particle‐size fractionation, density fractionation, aggregate fractionation, acid hydrolysis, different oxidation procedures, isolation of extractable lipids and phospholipid fatty acids, pyrolysis, and the determination of black C. Stability of OC was determined by ¹³C and ¹⁴C analyses. The main inputs of OC were plant litter (both sites) and deposition of fossil C likely from coal combustion and lignite dust (only Phaeozem).

The sequestration of carbon in soil is not completely understood, and quantitative information about the rates of soil organic carbon (SOC) turnover could improve understanding. We analyzed the effects of the uneven distribution of crop residues after harvest of silage maize on C and N losses (CO₂‐C, dissolved organic carbon (DOC) and nitrogen (DON), and NO₃^–) from a Haplic Phaeozem and on the occurrence of priming effects induced by the decomposition of accumulated maize residues. Soil columns were taken from a continuous maize (since 1961) field after harvest i) between maize stalk rows (M_bare), ii) within the maize rows including a standing maize stalk (M_stalk), and iii) from a continuous rye (since 1878) field after tillage (rye stalk and roots were mixed into the Ap horizon). The soil columns were incubated for 230 days at 8 °C with an irrigation rate of 2 mm 10^–2 M CaCl₂ per day. Natural ¹³C abundance was used to distinguish between maize‐derived C (in SOC and maize residues) and older C originating from former C₃ vegetation.The uneven distribution of maize residues resulted in a considerably increased heterotrophic activity within the maize rows as compared with soil between seed rows. Cumulative CO₂ production was 53.1 g CO₂‐C m^–2 for M_stalk and 23.3 g CO₂‐C m^–2 for M_bare. The contribution of maize‐derived C to the total CO₂ emission was 83 % (M_stalk) and 67 % (M_bare). Calculated as difference between CO₂‐C release from M_stalk and M_bare, 19 % of the maize residues (roots and stalk) in M_stalk were mineralized during the incubation period. There was no or only a marginal effect of the accumulation of maize residues in M_stalk on leaching of DOC, DON, and NO₃^–. Total DOC and DON leaching amounted to 2.5 g C m^–2 and 0.16 g N m^–2 for M_stalk and to 2.1 g C m^–2 and 0.12 g N m^–2 for M_bare. The contribution of maize‐derived C to DOC leaching was about 25 % for M_stalk and M_bare. Nitrate leaching amounted to 3.9 g NO₃^–‐N m^–2 for M_stalk and to 3.5 g NO₃^–‐N m^–2 for M_bare. There was no priming effect induced by the decomposition of fresh maize residues with respect to CO₂ or DOC production from indigenous soil organic carbon derived from C₃ vegetation.

Applying cattle slurry to soil may induce emissions of the greenhouse gases N₂O and CH₄. Our objective was to determine the effects of different application techniques (surface application and slit injection) of cattle (Bostaurus) slurry on the decomposition of slurry organic matter and the emissions of N₂O and CH₂. The effects of slurry application (43.6 m³ ha⁻¹) were studied for 9 wk under controlled laboratory conditions using a soil microcosm system with automated monitoring of the CO₂, N₂O, and CH₄ fluxes. The soil used was a silty loam (Ap horizon of a cambisol) with a constant water‐filled pore space of 67% during the experiment. About 38% of the organic matter applied with the slurry was decomposed within 9 wk. Production of CO₂ was not affected by the application technique. Emissions of N₂O and CH₄ from the injected slurry were significantly higher than from the surface‐applied slurry, probably because of restricted aeration at the injected‐slurry treatment. Total N₂O‐N emissions were 0.2% (surface application) and 3.3% (slit injection) of the slurry N added. Methane emission occurred only during the first few days following application. The total net flux of CH₄‐C for 2 wk was −12 g ha⁻¹ for the control (CH₄ uptake), 2 g ha⁻¹ for the surface‐applied slurry, and 39 g ha⁻¹ for the injected slurry. Slurry injection, which is recommended to reduce NH₃ volatilization, appears to increase emissions of the greenhouse gases N₂O and CH₄ from the fertilized fields.