Elevated CO2 concentration and nitrogen fertilisation effects on N2O and CH4 fluxes and biomass production of Phleum pratense on farmed peat soil

The effects of elevated CO₂ supply on N₂O and CH₄ fluxes and biomass production of Phleum pratense were studied in a greenhouse experiment. Three sets of 12 farmed peat soil mesocosms (10 cm dia, 47 cm long) sown with P. pratense and equally distributed in four thermo-controlled greenhouses were fertilised with a commercial fertiliser in order to add 2, 6 or 10 g N m⁻². In two of the greenhouses, CO₂ concentration was kept at atmospheric concentration (360 μmol mol⁻¹) and in the other two at doubled concentration (720 μmol mol⁻¹). Soil temperature was kept at 15 °C and air temperature at 20 °C. Natural lighting was supported by artificial light and deionized water was used to regulate soil moisture. Forage was harvested and the plants fertilised three times during the basic experiment, followed by an extra fertilisations and harvests. At the end of the experiment CH₄ production and CH₄ oxidation potentials were determined; roots were collected and the biomass was determined. From the three first harvests the amount of total N in the aboveground biomass was determined. N₂O and CH₄ exchange was monitored using a closed chamber technique and a gas chromatograph. The highest N₂O fluxes (on average, 255 μg N₂O m⁻² h⁻¹ during period IV) occurred just after fertilisation at high water contents, and especially at the beginning of the growing season (on average, 490 μg N₂O m⁻² h⁻¹ during period I) when the competition of vegetation for N was low. CH₄ fluxes were negligible throughout the experiment, and for all treatments the production and oxidation potentials of CH₄ were inconsequential. Especially at the highest rates of fertilisation, the elevated supply of CO₂ increased above- and below-ground biomass production, but both at the highest and lowest rates of fertilisation, decreased the total amount of N in the aboveground dry biomass. N₂O fluxes tended to be higher under doubled CO₂ concentrations, indicating that increasing atmospheric CO₂ concentration may affect N and C dynamics in farmed peat soil.     

Short-term effects of clearfelling on soil CO2, CH4, and N2O fluxes in a Sitka spruce plantation

We examined the effects of forest clearfelling on the fluxes of soil CO₂, CH₄, and N₂O in a Sitka spruce (Picea sitchensis (Bong.) Carr.) plantation on an organic-rich peaty gley soil, in Northern England. Soil CO₂, CH₄, N₂O as well as environmental factors such as soil temperature, soil water content, and depth to the water table were recorded in two mature stands for one growing season, at the end of which one of the two stands was felled and one was left as control. Monitoring of the same parameters continued thereafter for a second growing season. For the first 10 months after clearfelling, there was a significant decrease in soil CO₂ efflux, with an average efflux rate of 4.0 g m⁻² d⁻¹ in the mature stand (40-year) and 2.7 g m⁻² d⁻¹ in clearfelled site (CF). Clearfelling turned the soil from a sink (−0.37 mg m⁻² d⁻¹) for CH₄ to a net source (2.01 mg m⁻² d⁻¹). For the same period, soil N₂O fluxes averaged 0.57 mg m⁻² d⁻¹ in the CF and 0.23 mg m⁻² d⁻¹ in the 40-year stand. Clearfelling affected environmental factors and lead to higher daily soil temperatures during the summer period, while it caused an increase in the soil water content and a rise in the water table depth. Despite clearfelling, CO₂ remained the dominant greenhouse gas in terms of its greenhouse warming potential.     

Humic-rich peat extracts inhibit sulfate reduction, methanogenesis, and anaerobic respiration but not acetogenesis in peat soils of a temperate bog

To understand why anaerobic ombrotrophic peats can be very low in methane after drainage related afforestation, we analyzed the competition of sulfate reducing, humus reducing, and methanogenic microorganisms by incubating ombrotrophic peats of the Mer Bleue bog, Ontario. Sulfate, sulfide, and sulfate containing peat dissolved organic matter (DOM) from an afforested site were added in reduced and oxidized redox state. Sulfate and acetate concentrations were analyzed, bacterial sulfate reduction (BSR) and CO₂ and CH₄ production quantified, and results analyzed by ANOVA. DOM was characterized by Fourier transformed infrared and fluorescence spectroscopy and analyzed for trace elements. CH₄ production (116 nmol cm⁻³ d⁻¹) and BSR rate (102 nmol cm⁻³ d⁻¹) were similar in ‘controls’. BSR in treatments ‘sulfate’ (73 nmol cm⁻³ d⁻¹) and ‘sulfide’ (118 nmol cm⁻³ d⁻¹) did not significantly differ from ‘controls’ but addition of DOM significantly diminished BSR down to 0.4 nmol cm⁻³ d⁻¹ (Kruskal Wallis test, p < 0.05). CH₄ production decreased with sulfate (16%, not significant) and sulfide addition (40%, p < 0.05) and CO₂ production increased (treatment ‘sulfate’, p < 0.05). Addition of all DOM extracts (67 mg L⁻¹) almost completely suppressed methanogenesis and CO₂ production (p < 0.05), but acetate accumulated compared to the control (p < 0.05). The DOM applied contained carboxylic, aromatic and phenolic moieties and metal contents typical for peat humic substances. We conclude that a toxic effect of the intensely humified DOM occurred on both methanogenic and sulfate reducing bacteria (SRB) but not on fermenting microorganisms. As yet it is not clear what might cause such a toxic effect of DOM on SRB and archaea.     

Seasonal changes in the spatial structures of N2O, CO2, and CH4 fluxes from Acacia mangium plantation soils in Indonesia

We evaluated the spatial structures of nitrous oxide (N₂O), carbon dioxide (CO₂), and methane (CH₄) fluxes in an Acacia mangium plantation stand in Sumatra, Indonesia, in drier (August) and wetter (March) seasons. A 60 × 100-m plot was established in an A. mangium plantation that included different topographical elements of the upper plateau, lower plateau, upper slope and foot slope. The plot was divided into 10 × 10-m grids and gas fluxes and soil properties were measured at 77 grid points at 10-m intervals within the plot. Spatial structures of the gas fluxes and soil properties were identified using geostatistical analyses. Averaged N₂O and CO₂ fluxes in the wetter season (1.85 mg N m⁻² d⁻¹ and 4.29 g C m⁻² d⁻¹, respectively) were significantly higher than those in the drier season (0.55 mg N m⁻² d⁻¹ and 2.73 g C m⁻² d⁻¹, respectively) and averaged CH₄ uptake rates in the drier season (−0.62 mg C m⁻² d⁻¹) were higher than those in the wetter season (−0.24 mg C m⁻² d⁻¹). These values of N₂O fluxes in A. mangium soils were higher than those reported for natural forest soils in Sumatra, while CO₂ and CH₄ fluxes were in the range of fluxes reported for natural forest soils. Seasonal differences in these gas fluxes appears to be controlled by soil water content and substrate availability due to differing precipitation and mineralization of litter between seasons. N₂O fluxes had strong spatial dependence with a range of about 18 m in both the drier and wetter seasons. Topography was associated with the N₂O fluxes in the wetter season with higher and lower fluxes on the foot slope and on the upper plateau, respectively, via controlling the anaerobic-aerobic conditions in the soils. In the drier season, however, we could not find obvious topographic influences on the spatial patterns of N₂O fluxes and they may have depended on litter amount distribution. CO₂ fluxes had no spatial dependence in both seasons, but the topographic influence was significant in the drier season with lowest fluxes on the foot slope, while there was no significant difference between topographic positions in the wetter season. The distributions of litter amount and soil organic matter were possibly associated with CO₂ fluxes through their effects on microbial activities and fine root distribution in this A. mangium plantation.     

CH4 oxidation and emissions of CH4 and N2O from Lolium perenne swards under elevated atmospheric CO2

Emissions of N₂O and CH₄ and CH₄ oxidation rates were measured from Lolium perenne swards in a short-term study under ambient (36 Pa) and elevated (60 Pa) atmospheric CO₂ at the Free Air Carbon dioxide Enrichment experiment, Eschikon, Switzerland. Elevated pCO₂ increased (P<0.05) N₂O emissions from high N fertilised (11.2 g N m⁻²) swards by 69%, but had no significant effect on net emissions of CH₄. Application of ¹³C-CH₄ (11 μl l⁻¹; 11 at.% excess ¹³C) to closed chamber headspaces in microplots enabled determination of rates of ¹³C-CH₄ oxidation even when net CH₄ fluxes from main plots were positive. We found a significant interaction between fertiliser application rate and atmospheric pCO₂ on ¹³C-CH₄ oxidation rates that was attributed to differences in gross nitrification rates and C and N availability. CH₄ oxidation was slower and thought to be temporarily inhibited in the high N ambient pCO₂ sward. The most rapid CH₄ oxidation of 14.6 μg ¹³C-CH₄ m⁻² h⁻¹ was measured in the high fertilised elevated pCO₂ sward, and we concluded that either elevated pCO₂ had a stimulatory effect on CH₄ oxidation or inhibition of oxidation following fertiliser application was lowered under elevated pCO₂. Application of ¹⁴NH₄¹⁵NO₃ and ¹⁵NH₄¹⁵NO₃ (10 at.% excess ¹⁵N) to different replicates enabled determination of the respective contributions of nitrification and denitrification to N₂O emissions. Inhibition of CH₄ oxidation in the high fertilised ambient pCO₂ sward, due to competition between NH₃ and CH₄ for methane monooxygenase enzymes or toxic effects of NH₂OH or NO₂⁻ produced during nitrification, was hypothesised to increase gross nitrification (12.0 mg N kg dry soil⁻¹) and N₂O emissions during nitrification (327 mg ¹⁵N-N₂O m⁻² over 11 d). Our results indicate that increasing atmospheric concentrations of CO₂ may increase emissions of N₂O by denitrification, lower nitrification rates and either increase or decrease the ability of soil to act as a sink for atmospheric CH₄ depending on fertiliser management.     

Seasonal variation and fire effects on CH4, N2O and CO2 exchange in savanna soils of northern Australia

Tropical savanna ecosystems are a major contributor to global CO₂, CH₄ and N₂O greenhouse gas exchange. Savanna fire events represent large, discrete C emissions but the importance of ongoing soil-atmosphere gas exchange is less well understood. Seasonal rainfall and fire events are likely to impact upon savanna soil microbial processes involved in N₂O and CH₄ exchange. We measured soil CO₂, CH₄ and N₂O fluxes in savanna woodland (Eucalyptus tetrodonta/Eucalyptus miniata trees above sorghum grass) at Howard Springs, Australia over a 16 month period from October 2007 to January 2009 using manual chambers and a field-based gas chromatograph connected to automated chambers. The effect of fire on soil gas exchange was investigated through two controlled burns and protected unburnt areas. Fire is a frequent natural and management action in these savanna (every 1-2 years). There was no seasonal change and no fire effect upon soil N₂O exchange. Soil N₂O fluxes were very low, generally between −1.0 and 1.0 μg N m⁻² h⁻¹, and often below the minimum detection limit. There was an increase in soil NH₄⁺ in the months after the 2008 fire event, but no change in soil NO₃⁻. There was considerable nitrification in the early wet season but minimal nitrification at all other times.Savanna soil was generally a net CH₄ sink that equated to between −2.0 and −1.6 kg CH₄ ha⁻¹ y⁻¹ with no clear seasonal pattern in response to changing soil moisture conditions. Irrigation in the dry season significantly reduced soil gas diffusion and as a consequence soil CH₄ uptake. There were short periods of soil CH₄ emission, up to 20 μg C m⁻² h⁻¹, likely to have been caused by termite activity in, or beneath, automated chambers. Soil CO₂ fluxes showed a strong bimodal seasonal pattern, increasing fivefold from the dry into the wet season. Soil moisture showed a weak relationship with soil CH₄ fluxes, but a much stronger relationship with soil CO₂ fluxes, explaining up to 70% of the variation in unburnt treatments. Australian savanna soils are a small N₂O source, and possibly even a sink. Annual soil CH₄ flux measurements suggest that the 1.9 million km² of Australian savanna soils may provide a C sink of between −7.7 and −9.4 Tg CO₂-e per year. This sink estimate would offset potentially 10% of Australian transport related CO₂-e emissions. This CH₄ sink estimate does not include concurrent CH₄ emissions from termite mounds or ephemeral wetlands in Australian savannas.     

The inhibitory effect of difluoromethane on CH4 oxidation in reconstructed peat columns and side-effects on CO2 and N2O emissions at two water levels

Methane emissions from soils are the net result of two processes: methane (CH₄) production and CH₄ oxidation. In order to understand how both processes respond to environmental changes, it is necessary to distinguish between CH₄ production and oxidation. In bacterial cultures and small soil samples, difluoromethane (CH₂F₂) was found to inhibit CH₄ oxidation reversibly, without affecting CH₄ production. Hence, CH₂F₂ allows the study of CH₄ production directly and of CH₄ oxidation indirectly. To our knowledge, however, the inhibitory effect of CH₂F₂ within soil columns has not yet been evaluated. We therefore tested which CH₂F₂ concentration is needed for complete inhibition of CH₄ oxidation in reconstructed 28 cm high peat soil columns under different water levels (WL). We found that soil columns require considerably higher headspace CH₂F₂ concentrations for complete inhibition of CH₄ oxidation than small soil samples. Inhibition remained complete until ca. 24 h after CH₂F₂ exposure. Then, the inhibitory effect diminished. The time needed for the inhibitory effect to disappear depended on WL; at a low WL of −15 cm, the inhibitory effect declined slowly and oxidation rates recovered by 90% only after 12 days. At WL = −5 cm, CH₄ oxidation recovered much faster (90% recovery after ca. 3 days). Last, CH₂F₂ addition significantly decreased the N₂O emissions, whereas CO₂ emissions remained unaltered.     

Fluxes of CO2, CH4, and N2O in an alpine meadow affected by yak excreta on the Qinghai-Tibetan plateau during summer grazing periods

To assess the impacts of yak excreta patches on greenhouse gas (GHG) fluxes in the alpine meadow of the Qinghai-Tibetan plateau, methane (CH₄), carbon dioxide (CO₂), and nitrous oxide (N₂O) fluxes were measured for the first time from experimental excreta patches placed on the meadow during the summer grazing seasons in 2005 and 2006. Dung patches were CH₄ sources (average 586 μg m⁻² h⁻¹ in 2005 and 199 μg m⁻² h⁻¹ in 2006) during the investigation period of two years, while urine patches (average −31 μg m⁻² h⁻¹ in 2005 and −33 μg m⁻² h⁻¹ in 2006) and control plots (average −28 μg m⁻² h⁻¹ in 2005 and −30 μg m⁻² h⁻¹ in 2006) consumed CH₄. The cumulative CO₂ emission for dung patches was about 36-50% higher than control plots during the experimental period in 2005 and 2006. The cumulative N₂O emissions for both urine and dung patches were 2.1-3.7 and 1.8-3.5 times greater than control plots in 2005 and 2006, respectively. Soil water-filled pore space (WFPS) explained 35% and 36% of CH₄ flux variation for urine patches and control plots, respectively. Soil temperature explained 40-75% of temporal variation of CO₂ emissions for all treatments. Temporal N₂O flux variation in urine patches (34%), dung patches (48%), and control (56%) plots was mainly driven by the simultaneous effect of soil temperature and WFPS. Although yak excreta patches significantly affected GHG fluxes, their contributions to the whole grazing alpine meadow in terms of CO₂ equivalents are limited under the moderate grazing intensity (1.45 yak ha⁻¹). However, the contributions of excreta patches to N₂O emissions are not negligible when estimating N₂O emissions in the grazing meadow. In this study, the N₂O emission factor of yak excreta patches varied with year (about 0.9-1.0%, and 0.1-0.2% in 2005 and 2006, respectively), which was lower than IPCC default value of 2%.     

Fluxes of CO2, CH4 and N2O from drained organic soils in deciduous forests

We examined net greenhouse gas exchange at the soil surface in deciduous forests on soils with high organic contents. Fluxes of CO₂, CH₄ and N₂O were measured using dark static chambers for two consecutive years in three different forest types; (i) a drained and medium productivity site dominated by birch, (ii) a drained and highly productive site dominated by alder and (iii) an undrained and highly productive site dominated by alder. Although the drained sites had shallow mean groundwater tables (15 and 18 cm, respectively) their average annual rates of forest floor CO₂ release were almost twice as high compared to the undrained site (1.9±0.4 and 1.7±0.3, compared to 1.0±0.2 kg CO₂ m⁻² yr⁻¹). The average annual CH₄ emission was almost 10 times larger at the undrained site (7.6±3.1 compared to 0.9±0.5 g CH₄ m⁻² yr⁻¹ for the two drained sites). The average annual N₂O emissions at the undrained site (0.1±0.05 g N₂O m⁻² yr⁻¹) were lower than at the drained sites, and the emissions were almost five times higher at the drained alder site than at the drained birch site (0.9±0.35 compared to 0.2±0.11 g N₂O m⁻² yr⁻¹). The temporal variation in forest floor CO₂ release could be explained to a large extent by differences in groundwater table and air temperature, but little of the variation in the CH₄ and N₂O fluxes could be explained by these variables. The measured soil variables were only significant to explain for the within-site spatial variation in CH₄ and N₂O fluxes at the undrained swamp, and dark forest floor CO₂ release was not explained by these variables at any site. The between-site spatial variation was attributed to variations in drainage, groundwater level position, productivity and tree species for all three gases. The results indicate that N₂O emissions are of greater importance for the net greenhouse gas exchange at deciduous drained forest sites than at coniferous drained forest sites.     

Influence of warming and enchytraeid activities on soil CO2 and CH4 fluxes

To determine the sum of ‘direct’ and ‘indirect’ effects of climatic change on enchytraeid activity and C fluxes from an organic soil we assessed the influence of temperature (4, 10 and 15 °C incubations) on enchytraeid populations and soil CO₂ and CH₄ fluxes over 116 days. Moisture was maintained at 60% of soil dry weight during the experimental period and measurements of enchytraeid biomass and numbers, and CO₂ and CH₄ fluxes were made after 3, 16, 33, 44, 65, 86 and 116 days. Enchytraeid population numbers and biomass increased in all temperature treatments with the greatest increase produced at 15 °C (to over threefold initial values by day 86). Results also showed that enchytraeid activity increased CO₂ fluxes by 10.7±4.5, 3.4±4.0 and 26.8±2.6% in 4, 10 and 15 °C treatments, respectively, with the greatest CO₂ production observed at 15 °C for the entire 116 day incubation period (P<0.05). The soil respiratory quotient analyses at lower temperatures (i.e. 4-10 °C) gave a Q₁₀ of 1.7 and 1.9 with and without enchytraeids, respectively. At temperatures above 10 °C (i.e. 10-15 °C) Q₁₀ significantly increased (P<0.01) and was 25% greater in the presence of enchytraeids (Q₁₀=3.4) than without (Q₁₀=2.6). In contrast to CO₂ production, no significant relationships were observed between net CH₄ fluxes and temperature and only time showed a significant effect on CH₄ production (P<0.01).Total soil CO₂ production was positively linked with enchytraeid biomass and mean soil CO₂-C production was 77.01±6.05 CO₂-C μg mg enchytraeid tissue⁻¹ day⁻¹ irrespective of temperature treatment. This positive relationship was used to build a two step regression model to estimate the effects of temperature on enchytraeid biomass and soil CO₂ respiration in the field. Predictions of potential CO₂ production were made using enchytraeid biomass data obtained in the field from two upland grassland sites (Sourhope and Great Dun Fell at the Moor House Nature Reserve, both in the UK). The findings of this work suggest that a 5 °C increase in atmospheric temperature above mean ambient temperature could have the potential to produce a significant increase in enchytraeid biomass resulting in a near twofold increase in soil CO₂ release from both soil types. The interaction between temperature and soil biology will clearly be an important determinant of soil respiration responses to global warming.     

Desiccation and product accumulation constrain heterotrophic anaerobic respiration in peats of an ombrotrophic temperate bog

To gain insight into the effects of drying and rewetting events on anaerobic respiration in ombrotrophic peat soils, we investigated bacterial sulfate (SO₄) reduction and methane (CH₄) production in anaerobic incubations of intact peat microcores from 30 to 40 cm depth of Mer Bleue bog, Ontario/Canada. Concentrations of dissolved SO₄, carbon dioxide (CO₂), CH₄, acetate, and hydrogen (H₂) were recorded and net turnover rates calculated from regression. Gross rates of bacterial sulfate reduction were determined by ³⁵SO₄ tracer incubation. After incubation, the peat was dried and rewetted, with saturated peat serving as control. CO₂ production was initially rapid (up to <360 nmol cm^?3 d^?1) and slowed towards an endpoint of 2–3 mmol l^?1, which was only partly related to thresholds of Gibbs free energies of the involved processes. Acetate rapidly accumulated to levels of 600–800 μmol l^?1 and remained constant thereafter. CH₄ production (0–2.8 nmol cm^?3 d^?1) was small and delayed, even after SO₄ was depleted, by about 30–40 d. Hydrogenotrophic methanogenesis was endergonic and the process thus likely followed an acetotrophic pathway. Drying and rewetting replenished the SO₄ pool, enhanced SO₄ reduction rates and suppressed methanogenesis. The overall contribution of net SO₄ reduction and methanogenesis to the CO₂ production rate was small (0.5–22%) and only enhanced in replicates subjected to drying (35–62%). The major fraction of respiration in the incubated peat cores thus followed yet unidentified pathways.     

Soil chemistry versus environmental controls on production of CH4 and CO2 in northern peatlands

Rates of organic carbon mineralization (to CO₂ and CH₄) vary widely in peat soil. We transplanted four peat soils with different chemical composition into six sites with different environmental conditions to help resolve the debate about control of organic carbon mineralization by resource availability (e.g. carbon and nutrient chemistry) versus environmental conditions (e.g. temperature, moisture, pH). The four peat soils were derived from Sphagnum (bog moss). Two transplant sites were in mid‐boreal Alberta, Canada, two were in low‐boreal Ontario, Canada, and two were in the temperate United States. After 3 years in the field, CH₄ production varied significantly as a function of peat type, transplant site, and the type–site interaction. All four peat soils had very small rates of CH₄ production (< 20 nmol g^?1 day^?1) after transplant into two sites, presumably caused by acid site conditions (pH < 4.0). One peat soil had small CH₄ production rates regardless of transplant site. A canonical discriminant analysis revealed that large rates of CH₄ production (4000 nmol g^?1 day^?1) correlated with large holocellulose content, a large concentration of p‐hydroxyl phenolic compounds in the Klason lignin, and small concentrations of N, Ca and Mn in peat. Significant variation in rates of CO₂ production correlated positively with holocellulose content and negatively with N concentrations, regardless of transplant site. The temperature response for CO₂ production varied as a function of climate, being greater for peat formed in a cold climate, but did not apply to transplanted peat. Although we succeeded in elucidating some aspects of peat chemistry controlling production of CH₄ and CO₂ in Sphagnum‐derived peat soils, we also revealed idiosyncratic combinations of peat chemistry and site conditions that will complicate forecasting rates of peat carbon mineralization into the future.     

CH4 oxidation and N2O emissions at varied soil water-filled pore spaces and headspace CH4 concentrations

Emission of N₂O and CH₄ oxidation rates were measured from soils of contrasting (30-75%) water-filled pore space (WFPS). Oxidation rates of ¹³C-CH₄ were determined after application of 10 μl ¹³C-CH₄ l⁻¹ (10 at. % excess ¹³C) to soil headspace and comparisons made with estimates from changes in net CH₄ emission in these treatments and under ambient CH₄ where no ¹³C-CH₄ had been applied. We found a significant effect of soil WFPS on ¹³C-CH₄ oxidation rates and evidence for oxidation of 2.2 μg ¹³C-CH₄ d⁻¹ occurring in the 75% WFPS soil, which may have been either aerobic oxidation occurring in aerobic microsites in this soil or anaerobic CH₄ oxidation. The lowest ¹³C-CH₄ oxidation rate was measured in the 30% WFPS soil and was attributed to inhibition of methanotroph activity in this dry soil. However, oxidation was lowest in the wetter soils when estimated from changes in concentration of ¹²⁺¹³C-CH₄. Thus, both methanogenesis and CH₄ oxidation may have been occurring simultaneously in these wet soils, indicating the advantage of using a stable isotope approach to determine oxidation rates. Application of ¹³C-CH₄ at 10 μl ¹³C-CH₄ l⁻¹ resulted in more rapid oxidation than under ambient CH₄ conditions, suggesting CH₄ oxidation in this soil was substrate limited, particularly in the wetter soils. Application of and (80 mg N kg soil⁻¹; 9.9 at.% excess ¹⁵N) to different replicates enabled determination of the respective contributions of nitrification and denitrification to N₂O emissions. The highest N₂O emission (119 μg ¹⁴⁺¹⁵N-N₂O kg soil⁻¹ over 72 h) was measured from the 75% WFPS soil and was mostly produced during denitrification (18.1 μg ¹⁵N-N₂O kg soil⁻¹; 90% of ¹⁵N-N₂O from this treatment). Strong negative correlations between ¹⁴⁺¹⁵N-N₂O emissions, denitrified ¹⁵N-N₂O emissions and ¹³C-CH₄ concentrations (r=−0.93 to −0.95, N₂O; r=−0.87 to −0.95, denitrified ¹⁵N-N₂O; P<0.05) suggest a close relationship between CH₄ oxidation and denitrification in our soil, the nature of which requires further investigation.     

Carbon dioxide, nitrous oxide and methane dynamics in boreal organic agricultural soils with different soil characteristics

The annual carbon dioxide (CO₂), nitrous oxide (N₂O) and methane (CH₄) dynamics were measured with static chambers on two organic agricultural soils with different soil characteristics. Site 1 had a peat layer of 30 cm, with an organic matter (OM) content of 74% in the top 20 cm. Site 2 had a peat layer of 70 cm but an OM content of only 40% in the top 20 cm. On both sites there were plots under barley and grass and also plots where the vegetation was removed. All soils were net sources of CO₂ and N₂O, but they consumed atmospheric CH₄. Soils under barley had higher net CO₂ emissions (830 g CO₂-C m⁻² yr⁻¹) and N₂O emissions (848 mg N₂O-N m⁻² yr⁻¹) than those under grass (395 g CO₂-C m⁻³ yr⁻¹ and 275 mg N₂O-N m⁻² yr⁻¹). Bare soils had the highest N₂O emissions, mean 2350 mg N₂O-N m⁻² yr⁻¹. The mean CH₄ uptake rate from vegetated soils was 100 mg CH₄-C m⁻³ yr⁻¹ and from bare soils 55 mg CH₄-C m⁻² yr⁻¹. The net CO₂ emissions were higher from Site 2, which had a high peat bulk density and a low OM content derived from the addition of mineral soil to the peat during the cultivation history of that site. Despite the differences in soil characteristics, the mean N₂O emissions were similar from vegetated peat soils from both sites. However, bare soils from Site 2 with mineral soil addition had N₂O emissions of 2-9 times greater than those from Site 1. Site 1 consumed atmospheric CH₄ at a higher rate than Site 2 with additional mineral soil. N₂O emissions during winter were an important component of the N₂O budget even though they varied greatly, ranging from 2 to 99% (mean 26%) of the annual emission.     

Long-term (13 years) measurements of SO2 fluxes over a forest and their control by surface chemistry

Long-term fluxes of sulphur dioxide (SO₂) have been measured over a mixed suburban forest subjected to elevated SO₂ concentrations. The net exchange was shown to be highly dynamic with substantial periods of both upward and downward fluxes observed in excellent conditions for flux measurement. Upward fluxes constituted 30% of selected fluxes and appeared more frequently when the canopy was acidic. Upward fluxes were shown to be due to desorption from a drying surface or when ambient levels declined after periods of increased SO₂ exposure.The long term average SO₂ flux (F) was −59 ng SO₂ m⁻² s⁻¹ for the period 1997-2009 corresponding to an average SO₂ concentration of 12.3 μg SO₂ m⁻³ and a deposition velocity υ_d of 5 mm s⁻¹. The smallest deposition fluxes and υ_d were measured in dry conditions (−42 ng m⁻² s⁻¹ and 3.5 mm s⁻¹, resp.), which represented 57% of all cases. Wet canopies were more efficient sinks for SO₂ and a dew-wetted canopy had a smaller υ_d (6 mm s⁻¹) than a rain-wetted canopy (ca 10 mm s⁻¹). Seasonal variability reflected differences in chemical climate or canopy buffering properties. During the summer half-year when surface acidity was low due to higher NH₃/SO₂ ratios, a higher deposition efficiency (υ_d/υ_dmax) and lower non-stomatal resistance (R_w) were observed compared to winter conditions. Comparisons of R_c for different combinations of canopy wetness and surface acidity categories emphasized the importance of both factors in regulating the non-stomatal sinks of SO₂. Increased surface water acidity gradually led to a lower υ_d/υ_dmax and an increased R_c for all considered canopy wetness categories. The smallest υ_d/υ_dmax ratio and highest R_c were obtained for a dry canopy with high surface acidity. Conversely, a rain-wetted canopy was the most efficient sink for SO₂. The canopy sink strength was further enhanced by high friction velocities (u_*), optimizing the mechanical mixing into the canopy. Long-term trends were strongly coupled to changes in the NH₃/SO₂ ratio, which has clearly enhanced the deposition efficiency of SO₂ in recent years.     

Methane oxidation in boreal forest soils: kinetics and sensitivity to pH and ammonium

In soil incubation experiments we examined if there are differences in the kinetic parameters of atmospheric methane (CH₄) oxidation in soils of upland forests and forested peatlands. All soils showed net uptake of atmospheric CH₄. One of the upland forests included also managed (clear-cut with or without previous liming or N-fertilization) study plots. The CH₄ oxidation in the forested peat soil had a higher K_m (510 μl l⁻¹) and V_max (6.2 nmol CH₄ cm⁻³ h⁻¹) than the upland forest soils (K_m from 5 to 18 μl l⁻¹ and V_max from 0.15 to 1.7 nmol CH₄ cm⁻³ h⁻¹). The forest managements did not affect the K_m-values. At atmospheric CH₄ concentration, the upland forest soils had a higher CH₄ oxidation activity than the forested peat soil; at high CH₄ concentrations the reverse was true. Most of the soils oxidised CH₄ in the studied pH range from 3 to 7.5. The pH optimum for CH₄ oxidation varied from 4 to 7.5. Some of the soils had a pH optimum for CH₄ oxidation that was above their natural pH. The CH₄ oxidation in the upland forest soils and in the peat soil did not differ in their sensitivities to (NH₄)₂SO₄ or K₂SO₄ (used as a non-ammonium salt control). Inhibition of CH₄ oxidation by (NH₄)₂SO₄ resulted mainly from a general salt effect (osmotic stress) though NH₄⁺ did have some additional inhibitory properties. Both salts were better inhibitors of CH₄ oxidation than respiration. The differences in the CH₄ oxidation kinetics in the forested peat soil and in the upland forest soils reveal that there are differences in the physiologies of the CH₄ oxidisers in these soils.     

Simultaneous inhibition of CH4 efflux and stimulation of sulphate reduction in peat subject to simulated acid rain

Acid rain sulphate (SO₄²⁻) deposition is a known suppressant of methane (CH₄) emission from wetlands. However, the hypothesised mechanism responsible for this important biogeochemical interaction, competitive exclusion of methanogens by dissimilatory SO₄²⁻ reducing bacteria (SRB), lacks supporting evidence. Here, we present data from an acid rain simulation experiment in the Moidach More peat bog of NE Scotland that strengthens this hypothesis. We report a tenfold increase in estimated SO₄²⁻ reduction during periods when measured CH₄ emission rates were suppressed relative to controls receiving only one-tenth the SO₄²⁻ of treated plots, but no treatment effect on potential methane oxidation. This tenfold increase in estimated SO₄²⁻ reduction indicates the presence of a more active population of SRB in plots where CH₄ emissions were reduced by over 30%.     

Emission of CO2, CH4 and N2O from lakeshore soils in an Antarctic dry valley

We measured soil profile concentrations and emission of CO₂, CH₄ and N₂O from soils along a lakeshore in Garwood Valley, Antarctica, to assess the extent and biogeochemical significance of biogenic gas emission to C and N cycling processes. Simultaneous emission of all three gases from the same site indicated that aerobic and anaerobic processes occurred in different layers or different parts of each soil profile. The day and location of high gas concentrations in the soil profile corresponded to those having high gas emission, but the pattern of concentration with depth in the soil profile was not consistent across sites. That the highest gas concentrations were not always in the deepest soil layer suggests either limited production or gas diffusion in the deeper layers. Emission of CO₂ was as high as 47 μmol m⁻² min⁻¹ and was strongly related to soil temperature. Soil respiration differed significantly according to location on the lakeshore, suggesting that factors other than environmental variables, such as the amount and availability of O₂ and nutrients, play an important role in C mineralization processes in these soils. High surface emission (maximum: 15 μmol m⁻² min⁻¹) and profile gas concentration (maximum: 5780 μL L⁻¹) of CH₄ were at levels comparable to those in resource-rich temperate ecosystems, indicating an active indigenous population of methanogenic organisms. Emission of N₂O was low and highly variable, but the presence of this gas and NO₃ in some of the soils suggest that denitrification and nitrification occur there. No significant relationships between N₂O emission and environmental variables were found. It appears that considerable C and N turnover occurs in the lakeshore soils, and accurate accounting will require measurements of aerobic and anaerobic mineralization. The production and emission of biogenic gases confirm the importance of these soils as hotspots of biological activity in the dry valleys and probable reservoirs of biological diversity.     

Emission of N2O, N2 and CO2 from soil fertilized with nitrate: effect of compaction, soil moisture and rewetting

Soil compaction and soil moisture are important factors influencing denitrification and N₂O emission from fertilized soils. We analyzed the combined effects of these factors on the emission of N₂O, N₂ and CO₂ from undisturbed soil cores fertilized with (150 kg N ha⁻¹) in a laboratory experiment. The soil cores were collected from differently compacted areas in a potato field, i.e. the ridges (ρ_D=1.03 g cm⁻³), the interrow area (ρ_D=1.24 g cm⁻³), and the tractor compacted interrow area (ρ_D=1.64 g cm⁻³), and adjusted to constant soil moisture levels between 40 and 98% water-filled pore space (WFPS).High N₂O emissions were a result of denitrification and occurred at a WFPS≥70% in all compaction treatments. N₂ production occurred only at the highest soil moisture level (≥90% WFPS) but it was considerably smaller than the N₂O-N emission in most cases. There was no soil moisture effect on CO₂ emission from the differently compacted soils with the exception of the highest soil moisture level (98% WFPS) of the tractor-compacted soil in which soil respiration was significantly reduced. The maximum N₂O emission rates from all treatments occurred after rewetting of dry soil. This rewetting effect increased with the amount of water added. The results show the importance of increased carbon availability and associated respiratory O₂ consumption induced by soil drying and rewetting for the emissions of N₂O.     

Carbon exchange in a freshwater marsh in the Sanjiang Plain, northeastern China

Northern wetlands are critically important to global change because of their role in modulating atmospheric concentrations of greenhouse gases, especially CO₂ and CH₄. At present, continuous observations for CO₂ and CH₄ fluxes from northern wetlands in Asia are still very limited. In this paper, two growing season measurements for CO₂ flux by eddy covariance technique and CH₄ flux by static chamber technique were conducted in 2004 and 2005, at a permanently inundated marsh in the Sanjiang Plain, northeastern China. The seasonal variations of CO₂ exchange and CH₄ flux and the environmental controls on them were investigated. During the growing seasons, large variations in net ecosystem CO₂ exchange (NEE) and gross ecosystem productivity (GEP) were observed with the range of −4.0 to 2.2 (where negative exchange is a gain of carbon from the atmosphere) and 0-7.6 g C m⁻² d⁻¹, respectively. Ecosystem respiration (RE) displayed relatively smooth seasonal pattern with the range of 0.8-4.2 g C m⁻² d⁻¹. More than 70% of the total GEP was consumed by respiration, which resulted in a net CO₂ uptake of 143 ± 9.8 and 100 ± 9.2 g C m⁻² for the marsh over the growing seasons of 2004 and 2005, respectively. A significant portion of the accumulated NEE-C was lost by CH₄ emission during the growing seasons, indicating the great potential of CH₄ emission from the inundated marsh. Air temperature and leaf area index jointly affected the seasonal variation of GEP and the seasonal dynamic of RE was mainly controlled by soil temperature and leaf area index. Soil temperature also exerted the dominant influence over variation of CH₄ flux while no significant relationship was found between CH₄ emission and water table level. The close relationships between carbon fluxes and temperature can provide insights into the response of marsh carbon exchange to a changing climate. Future long term flux measurements over the freshwater marsh ecosystems are undoubtedly necessary.