Carbon turnover in peatland mesocosms exposed to different water table levels

Changes of water table position influence carbon cycling in peatlands, but effects on the sources and sinks of carbon are difficult to isolate and quantify in field investigations due to seasonal dynamics and covariance of variables. We thus investigated carbon fluxes and dissolved carbon production in peatland mesocosms from two acidic and oligotrophic peatlands under steady state conditions at two different water table positions. Exchange rates and CO₂, CH₄ and DOC production rates were simultaneously determined in the peat from diffusive-advective mass-balances of dissolved CO₂, CH₄ and DOC in the pore water. Incubation experiments were used to quantify potential CO₂, CH₄, and DOC production rates. The carbon turnover in the saturated peat was dominated by the production of DOC (10–15 mmol m^–2 d^–1) with lower rates of DIC (6.1–8.5 mmol m^–2 d^–1) and CH₄ (2.2–4.2 mmol m^–2 d^–1) production. All production rates strongly decreased with depth indicating the importance of fresh plant tissue for dissolved C release. A lower water table decreased area based rates of photosynthesis (24–42%), CH₄ production (factor 2.5–3.5) and emission, increased rates of soil respiration and microbial biomass C, and did not change DOC release. Due to the changes in process rates the C net balance of the mesocosms shifted by 36 mmol m^–2 d^–1. According to our estimates the change in C mineralization contributed most to this change. Anaerobic rates of CO₂ production rates deeper in the peat increased significantly by a factor of 2–3.5 (DOC), 2.9–3.9 (CO₂), and 3–14 (CH₄) when the water table was lowered by 30 cm. This phenomenon might have been caused by easing an inhibiting effect by the accumulation of CO₂ and CH₄ when the water table was at the moss surface.     

The importance of floating peat to methane fluxes from flooded peatlands

The effect of flooding on methane (CH₄) fluxes was studied through the construction of an experimental reservoir in a boreal forest wetland at the Experimental Lakes Area in northwestern Ontario. Prior to flooding, the peatland surface was a small source of CH₄ to the atmosphere (1.0± SD of 2.3 mg CH₄ m^–2 d^–1). After flooding, CH₄ fluxes from the submerged peat surface increased to 64±68 mg CH4 m^–2 d^–1 CH₄ bubbles within the submerged peat caused about 1/3 of the peat to float. Fluxes from these floating peat islands were much higher (440±350 mg CH₄ m^–2 d^–2) than from both the pre-flood (undisturbed) and the post-flood (submerged) peat surfaces.The high fluxes of CH₄ from the floating peat surfaces may be explained by a number of factors known to affect the production and consumption of CH₄ in peat. In floating peat, however, these factors are particularly enhanced and include decreased oxidation of CH₄ due to the loss of aerobic habitat normally found above the water table of undisturbed peat and to increased peat temperatures. The extremely high fluxes associated with newly lifted peat may decrease as the islands age. However, CH₄ flux rates from floating peat islands that were several years old still far exceeded those from undisturbed peat surfaces and from the water surface of a newly created reservoir.     

Control of carbon mineralization to CH4 and CO2 in anaerobic,Sphagnum-derived peat from Big Run Bog,West Virginia

The mineralization of organic carbon to CH₄ and CO₂ inSphagnum-derived peat from Big Run Bog, West Virginia, was measured at 4 times in the year (February, May, September, and November) using anaerobic, peat-slurry incubations. Rates of both CH₄ production and CO₂ production changed seasonally in surface peat (0–25 cm depth), but were the same on each collection date in deep peat (30–45 cm depth). Methane production in surface peat ranged from 0.2 to 18.8 mol mol(C)^–1 hr^–1 (or 0.07 to 10.4 g(CH₄) g^–1 hr^–1) between the February and September collections, respectively, and was approximately 1 mol mol(C)^–1 hr^–1 in deep peat. Carbon dioxide production in surface peat ranged from 3.2 to 20 mol mol(C)^–1 hr^–1 (or 4.8 to 30.3 g(CO₂) g^–1 hr^–1) between the February and September collections, respectively, and was about 4 mol mol(C)^–1 hr^–1 in deep peat. In surface peat, temperature the master variable controlling the seasonal pattern in CO₂ production, but the rate of CH₄ production still had the lowest values in the February collection even when the peat was incubated at 19°C. The addition of glucose, acetate, and H₂ to the peat-slurry did not stimulate CH₄ production in surface peat, indicating that CH₄ production in the winter was limited by factors other than glucose degradation products. The low rate of carbon mineralization in deep peat was due, in part, to poor chemical quality of the peat, because adding glucose and hydrogen directly stimulated CH₄ production, and CO₂ production to a lesser extent. Acetate was utilized in the peat by methanogens, but became a toxin at low pH values. The addition of SO₄ ^2– to the peat-slurry inhibited CH4 production in surface peat, as expected, but surprisingly increased carbon mineralization through CH4 production in deep peat. Carbon mineralization under anaerobic conditions is of sufficient magnitude to have a major influence on peat accumulation and helps to explain the thin (< 2 m deep), old (> 13,000 yr) peat deposit found in Big Run Bog.     

Fluxes of N2O,CH4 and CO2 on afforested boreal agricultural soils

After drainage of natural boreal peatlands, the decomposition of organic matter increases and peat soil may turn into a net source of CO₂ and N₂O, whereas CH₄ emission is known to decrease. Afforestation is a potential mitigation strategy to reduce greenhouse gas emission from organic agricultural soils. A static chamber technique was used to evaluate the fluxes of CH₄, N₂O and CO₂ from three boreal organic agricultural soils in western Finland, afforested 1, 6 or 23 years before this study. The mean emissions of CH₄ and N₂O during the growing seasons did not correlate with the age of the tree stand. All sites were sources of N₂O. The highest daily N₂O emission during the growing season, measured in the oldest site, was as high as 29 mg N₂O m^–2d^–1. In general, organic agricultural soils are sinks for methane. Here, the oldest site acted as a small sink for methane, whereas the two youngest afforested organic soils were sources for methane with maximum emission rates (up to 154 mg m^–2d^–1) similar to those reported for minerogenous natural peatlands. Soil respiration rates decreased with the age of the forest. The high soil respiration in the younger sites, probably resulted from the high biomass production of herbs, could create soil anaerobiosis and increase methane production. Our results show that afforestation of agricultural peat soils does not abruptly terminate the N₂O emissions during the first two decades, and afforestation can even enhance methane emission for a few years. The carbon accumulation in the developing tree stand can partly compensate the carbon loss from soil.     

Mineralization rates of peat from eroding peat islands in reservoirs

Reservoirs are sources of greenhouses gases to the atmosphere, primarily due to organic carbon mineralization in flooded plants and soils to carbon dioxide (CO₂) and methane (CH₄). Floating peat islands are common in reservoirs that inundated peatlands. These islands can decompose on mass, or small pieces of peat can erode from islands to decompose in the water column or on the bottom of reservoirs. Here we used large 450 liter sealed enclosures to measure mineralization rates of small peat pieces and larger peat blocks collected from floating peat islands. Mineralization rates were calculated by quantifying dissolved inorganic carbon (DIC), CO₂ and CH₄ accumulation within the water and headspace of the enclosures over time. We found that peat did decompose under water, but rates of mineralization of peat pieces were not different than rates of mineralization of larger peat blocks. Mineralization rates ranged between 59 and l40 g C g^–1 d^–1. Peat pieces acidified the water, shifting the bicarbonate equilibrium to almost exclusively dissolved CO₂, which was then readily able to flux to the atmosphere. We estimated that 2.4–5.6% of peat carbon was mineralized annually, suggesting that fluxes of CO₂ and CH₄ from reservoirs that flood peatlands could last at minimum 18–42 years from this carbon source alone.     

Methane emissions from fen,bog and swamp peatlands in Quebec

A static chamber technique was used weekly from spring thaw to winter freezing to measure methane emissions from 10 sites representing subarctic fens and temperate swamps and bogs. Rates of < 200 mg CH₄ m^–2 d^–1 were recorded in subarctic fens: within-site emissions were primarily controlled by the evolution of the peat thermal regime, though significant releases during spring thaw were recorded at some sites. Between subarctic fens, topography and water table elevation were important controls on methane emissions, with the general sequence: pool = horizontal fen> string. Emission rates from the 2 swamp sites were lower (< 20 mg CH₄ m^–2 d^–1 ), except during the spring thaw and when the sites were saturated. The low water table ( < 80 cm depth) in abnormally dry years reduced emission rates; rates were also low from a swamp site which had been drained and cleared of vegetation for horticulture. Methane emission rates were also low (< 5 mg CH₄ m^–2 d^–1) from 2 ombrotrophic bog sites. Laboratory measurements of rates of methane production under anaerobic conditions and methane consumption under aerobic conditions revealed that production rates were generally highest in the surface layers (0 to 2.5 cm depth); production was high in the fens and very low in the bogs. The swamp samples were able to produce methane under anaerobic conditions, but were also able to consume methane under aerobic conditions. Annual methane emission rates are estimated to be 1 to 10 g CH₄ m^–2 from the fens, 1 to 4 g CH4 m^–2 from the swamps and <0.2 g CH₄ m^–2 from the bogs and drained swamp.     

A three-year study of controls on methane emissions from two Michigan peatlands

We investigate temporal changes in methane emissions over a three-year period from two peatlands in Michigan. Mean daily fluxes ranged from 0.6–68.4 mg CH₄ m^–2d^–1 in plant communities dominated by Chamaedaphne calyculata, an eficaceous shrub, to 11.5–209 mg CH₄ m^–2d^–1 in areas dominated by plants with aerenchymatous tissues, such as Carex oligosperma and Scheuchzeria palustris. Correlations between methane flux and water table position were significant at all sites for one annual cycle when water table fluctuations ranged from 15 cm above to 50 cm below the peat surface. Correlations were not significant during the second and third annual periods with smaller water table fluctuations. Methane flux was strongly correlated with peat temperatures at –5 to –40 cm (r _s = 0.82 to 0.98) for all three years at sites with flora acting as conduits for methane transport. At shrub sites, the correlations between methane flux and peat temperature were weak to not significant during the first two years, but were strong in the third year.Low rates of methane consumption (–0.2 to –1.5 mg CH₄ m^–2 d^–1 ) were observed at shrub sites when the water table was below –20 cm, while sites with plants capable of methane transport always had positive net fluxes of methane. The methane oxidizing potential at both types of sites was confirmed by peat core experiments. The results of this study indicate that methane emissions occur at rates that cannot be explained by diffusion alone; plant communities play a significant role in altering methane flux from peatland ecosystems by directly transporting methane from anaerobic peat to the atmosphere.     

Winter CO2 CH4 and N2O fluxes on some natural and drained boreal peatlands

CO₂ and CH₄ fluxes during the winter were measured at natural and drained bog and fen sites in eastern Finland using both the closed chamber method and calculations of gas diffusion along a concentration gradient through the snowpack. The snow diffusion results were compared with those obtained by chamber, but the winter flux estimates were derived from chamber data only. CH₄ emissions from a poor bog were lower than those from an oligotrophic fen, while both CO₂ and CH₄ fluxes were higher in theCarex rostrata- occupied marginal (lagg) area of the fen than in the slightly less fertile centre. Average estimated winter CO₂-C losses from virgin and drained forested peatlands were 41 and 68 g CO₂-C m^–2, respectively, accounting for 23 and 21% of the annual total CO₂ release from the peat. The mean release of CH₄-C was 1.0 g in natural bogs and 3.4 g m^–2 in fens, giving rise to winter emissions averaging to 22% of the annual emission from the bogs and 10% of that from the fens. These wintertime carbon gas losses in Finnish natural peatlands were even greater than reported average long-term annual C accumulation values (less than 25g C m^–2). The narrow range of 10–30% of the proportion of winter CO₂ and CH₄ emissions from annual emissions found in Finnish peatlands suggest that a wider generalization in the boreal zone is possible. Drained forested bogs emitted 0.3 g CH₄-C m^–2 on the average, while the effectively drained fens consumed an average of 0.01 g CH₄-C m^–2. Reason for the low CH₄. efflux or net oxidation in drained peatlands probably lies in low substrate supply and thus low CH₄ production in the anoxic deep peat layers. N₂O release from a fertilized grassland site in November–May was 0.7 g N₂O m^–2, accounting for 38% of the total annual emission, while a forested bog released none and two efficiently drained forested fens 0.09 (28% of annual release) and 0.04 g N₂O m^–2 (27%) during the winter, respectively.     

Production of CO2 in Soil Profiles of a California Annual Grassland

Soils play a key role in the global cycling of carbon (C), storing organic C, and releasing CO₂ to the atmosphere. Although a large number of studies have focused on the CO₂ flux at the soil–air interface, relatively few studies have examined the rates of CO₂ production in individual layers of a soil profile. Deeper soil horizons often have high concentrations of CO₂ in the soil air, but the sources of this CO₂ and the spatiotemporal dynamics of CO₂ production throughout the soil profile are poorly understood. We studied CO₂ dynamics in six soil profiles arrayed across a grassland hillslope in coastal southern California. Gas probes were installed in each profile and gas samples were collected weekly or biweekly over a three-year period. Using soil air CO₂ concentration data and a model based on Fick’s law of diffusion, we modeled the rates of CO₂ production with soil profile depth. The CO₂ diffusion constants were checked for accuracy using measured soil air ²²²Rn activities. The modeled net CO₂ production rates were compared with CO₂ fluxes measured at the soil surface. In general, the modeled and measured net CO₂ fluxes were very similar although the model consistently underestimated CO₂ production rates in the surficial soil horizons when the soils were moist. Profile CO₂ production rates were strongly affected by the inter- and intra-annual variability in rainfall; rates were generally 2–10 times higher in the wet season (December to May) than in the dry season (June to November). The El Niño event of 1997–1998, which brought above-average levels of rainfall to the study site, significantly increased CO₂ production in both the surface and subsurface soil horizons. Whole profile CO₂ production rates were approximately three times higher during the El Niño year than in the following years of near-average rainfall. During the dry season, when the net rates of CO₂ flux from the soil profiles are relatively low (4–11 mg C– CO₂ m⁻² h⁻¹), 20%–50% of the CO₂ diffusing out of the profiles appears to originate in the relatively moist soil subsurface (defined here as those horizons below 40 cm in depth). The natural abundance ¹⁴C signatures of the CO₂ and soil organic C suggest that the subsurface CO₂ is derived from the microbial mineralization of recent organic C, possibly dissolved organic C transported to the subsurface horizons during the wet season.     

Methane dynamics of recolonized cutover minerotrophic peatland: Implications for restoration

In North America, mulching of vacuum-harvested sites combined with blocking of the drainage system is widely used for peatland restoration to accelerate Sphagnum establishment. However, peat extraction in fen peatlands or exposure of deeper minerotrophic peat layers results in soil chemistry that is less suitable for re-establishment of Sphagnum moss. In this situation, restoration of plant species characteristic of minerotrophic peatlands is desirable to return the site to a carbon accumulating system. In these cases, it may be worthwhile to maintain spontaneously revegetating species as part of restoration if they provide desirable ecosystem functions. We studied the role of six spontaneously recolonizing vegetation communities for methane (CH₄) emissions and pore water CH₄ concentration for two growing seasons (2008 and 2009) at an abandoned minerotrophic peatland in southeastern Quebec. We then compared the results with bare peat and adjacent natural fen vegetation. Communities dominated by Eriophorum vaginatum, Carex aquatilis and Typha latifolia had CH₄ flux an order of magnitude greater than other cutover vegetation types and natural sites. In contrast, Scirpus atrocinctus and Equisetum arvense had CH₄ emission rates lower than natural hollow vegetation. We found seasonal average water table and vegetation volume had significant correlation with CH₄ flux. Water table and soil temperature were significantly correlated with CH₄ flux at plots where the water table was near or above the surface. Pore water CH₄ concentration suggests that CH₄ is being produced at the cutover peatland and that low measured fluxes likely result from substantial oxidation of CH₄ in the unsaturated zone. Understanding ecosystem functions of spontaneously recolonizing species on cutover fens can be used to help make decisions about the inclusion of these communities for future restoration measures.     

Evidence for older carbon loss with lowered water tables and changing plant functional groups in peatlands

A small imbalance in plant productivity and decomposition accounts for the carbon (C) accumulation capacity of peatlands. As climate changes, the continuity of peatland net C storage relies on rising primary production to offset increasing ecosystem respiration (ER) along with the persistence of older C in waterlogged peat. A lowering in the water table position in peatlands often increases decomposition rates, but concurrent plant community shifts can interactively alter ER and plant productivity responses. The combined effects of water table variation and plant communities on older peat C loss are unknown. We used a full-factorial 1-m³ mesocosm array with vascular plant functional group manipulations (Unmanipulated Control, Sedge only, and Ericaceous only) and water table depth (natural and lowered) treatments to test the effects of plants and water depth on CO₂ fluxes, decomposition, and older C loss. We used Δ¹⁴C and δ¹³C of ecosystem CO₂ respiration, bulk peat, plants, and porewater dissolved inorganic C to construct mixing models partitioning ER among potential sources. We found that the lowered water table treatments were respiring C fixed before the bomb spike (1955) from deep waterlogged peat. Lowered water table Sedge treatments had the oldest dissolved inorganic ¹⁴C signature and the highest proportional peat contribution to ER. Decomposition assays corroborated sustained high rates of decomposition with lowered water tables down to 40 cm below the peat surface. Heterotrophic respiration exceeded plant respiration at the height of the growing season in lowered water table treatments. Rates of gross primary production were only impacted by vegetation, whereas ER was affected by vegetation and water table depth treatments. The decoupling of respiration and primary production with lowered water tables combined with older C losses suggests that climate and land-use-induced changes in peatland hydrology can increase the vulnerability of peatland C stores.     

Effects of soil phosphorus availability,temperature and moisture on soil respiration in Eucalyptus pauciflora forest

Rates of soil respiration (CO₂ efflux) were measured for a year in a mature Eucalyptus pauciflora forest in unfertilized and phosphorus-fertilized plots. Soil CO₂ efflux showed a distinct seasonal trend, and average daily rates ranged from 124 to 574 mg CO₂ m^–2 hr^–1. Temperature and moisture are the main variables that cause variation in soil CO₂ efflux; hence their effects were investigated over a year so as to then differentiate the treatment effect of phosphorus (P) nutrition.Soil temperature had the greatest effect on CO₂ efflux and exhibited a highly significant logarithmic relationship (r² = 0.81). Periods of low soil and litter moisture occurred during summer when temperatures were greater than 10 °C, and this resulted in depression of soil CO₂ efflux. During winter, when temperatures were less than 10 °C, soil and litter moisture were consistently high and thus their variation had little effect on soil CO₂ efflux. A multiple regression model including soil temperature, and soil and litter moisture accounted for 97% of the variance in rates of CO₂ efflux, and thus can be used to predict soil CO₂ efflux at this site with high accuracy. Total annual efflux of carbon from soil was estimated to be 7.11 t C ha^–1 yr^–1. The model was used to predict changes in this annual flux if temperature and moisture conditions were altered. The extent to which coefficients of the model differ among sites and forest types requires testing.Increased soil P availability resulted in a large increase in stem growth of trees but a reduction in the rate of soil CO₂ efflux by approximately 8%. This reduction is suggested to be due to lower root activity resulting from reduced allocation of assimilate belowground. Root activity changed when P was added to microsites within plots, and via the whole tree root system at the plot level. These relationships of belowground carbon fluxes with temperature, moisture and nutrient availability provide essential information for understanding and predicting potential changes in forest ecosystems in response to land use management or climate change.     

Sphagnum production and decomposition in a restored cutover peatland

Natural peatlands represent a long-termsink of atmospheric carbon dioxide(CO₂), however, drained and extractedpeatlands can represent a source ofatmospheric CO₂. The restoration ofSphagnum mosses on abandoned milledpeatlands has the potential to sequesteratmospheric CO₂ thereby returning thepeatland to a peat accumulating system.Micrometeorological and chambermeasurements of net ecosystem CO₂exchange are proven methods forinvestigating production and decompositionprocesses in both natural, extracted, andrestored peatlands. However, this approachis relatively expensive because ofinfrastructure and human resources that notonly limits potential use for ecologicalmanagers but it limits the number of sitesthat can be monitored due to high spatialvariability. Here we present crank wire anddestructive sampling productionmeasurements, litter bag decompositionmeasurements and measurements of netecosystem CO₂ exchange made in arestored peatland and natural peatlandsites nearby. The objectives were to assessproduction and decomposition rates in thetwo systems as well as to compare thedifferent measurements techniques.Estimates of Sphagnum fuscumproduction at a restored peatland, usingthe different methods, followed the trend:crank wire < destructive sampling < gasexchange, with the two last methodsproviding comparable estimates. Productionestimates using crank wires in cutover peatsurfaces with a thin newly formed Sphagnum mat were shown unreliable due topeat subsidence. Results using thedestructive sampling method suggest thatSphagnum production varies betweenspecies (S. fuscum > S.capillifolium) according to their abilityto withstand harsh conditions on restoredpeat surfaces. Decomposition rate was alsosignificantly greater (p<0.05) for S. capillifolium than S. fuscum,resulting in an overall plant accumulationgreater for S. fuscum. Although therestored surfaces were fairly young,production rates estimated on cutoversurfaces that were fully covered with athin Sphagnum mat compared withproduction rates observed in natural sitesnearby.     

Drainage increases CO2 and N2O emissions from tropical peat soils

Tropical peatlands are vital ecosystems that play an important role in global carbon storage and cycles. Current estimates of greenhouse gases from these peatlands are uncertain as emissions vary with environmental conditions. This study provides the first comprehensive analysis of managed and natural tropical peatland GHG fluxes: heterotrophic (i.e. soil respiration without roots), total CO₂ respiration rates, CH₄ and N₂O fluxes. The study documents studies that measure GHG fluxes from the soil (n = 372) from various land uses, groundwater levels and environmental conditions. We found that total soil respiration was larger in managed peat ecosystems (median = 52.3 Mg CO₂ ha^?1 year^?1) than in natural forest (median = 35.9 Mg CO₂ ha^?1 year^?1). Groundwater level had a stronger effect on soil CO₂ emission than land use. Every 100 mm drop of groundwater level caused an increase of 5.1 and 3.7 Mg CO₂ ha^?1 year^?1 for plantation and cropping land use, respectively. Where groundwater is deep (≥0.5 m), heterotrophic respiration constituted 84% of the total emissions. N₂O emissions were significantly larger at deeper groundwater levels, where every drop in 100 mm of groundwater level resulted in an exponential emission increase (exp(0.7) kg N ha^?1 year^?1). Deeper groundwater levels induced high N₂O emissions, which constitute about 15% of total GHG emissions. CH₄ emissions were large where groundwater is shallow; however, they were substantially smaller than other GHG emissions. When compared to temperate and boreal peatland soils, tropical peatlands had, on average, double the CO₂ emissions. Surprisingly, the CO₂ emission rates in tropical peatlands were in the same magnitude as tropical mineral soils. This comprehensive analysis provides a great understanding of the GHG dynamics within tropical peat soils that can be used as a guide for policymakers to create suitable programmes to manage the sustainability of peatlands effectively.     

Ecosystem Respiration in a Cool Temperate Bog Depends on Peat Temperature But Not Water Table

Ecosystem respiration (ER) is an important but poorly understood part of the carbon (C) budget of peatlands and is controlled primarily by the thermal and hydrologic regimes. To establish the relative importance of these two controls for a large ombrotrophic bog near Ottawa, Canada, we analyzed ER from measurements of nighttime net ecosystem exchange of carbon dioxide (CO₂) determined by eddy covariance technique. Measurements were made from May to October over five years, 1998 to 2002. Ecosystem respiration ranged from less than 1 μmol CO₂ m⁻² s⁻¹ in spring (May) and fall (late October) to 2–4 μmol CO₂ m⁻² s⁻¹ during mid-summer (July-August). As anticipated, there was a strong relationship between ER and peat temperatures (r² = 0.62). Q₁₀ between 5° to 15°C varied from 2.2 to 4.2 depending upon the choice of depth where temperature was measured and location within a hummock or hollow. There was only a weak relationship between ER and water-table depth (r² = 0.11). A laboratory incubation of peat cores at different moisture contents showed that CO₂ production was reduced by drying in the surface samples, but there was little decrease in production due to drying from below a depth of 30 cm. We postulate that the weak correlation between ER and water table position in this peatland is primarily a function of the bog being relatively dry, with water table varying between 30 and 75 cm below the hummock tops. The dryness gives rise to a complex ER response to water table involving i) compensations between production of CO₂ in the upper and lower peat profile as the water table falls and ii) the importance of autotrophic respiration, which is relatively independent of water-table position.     

Soil and total ecosystem respiration in agricultural fields: effect of soil and crop type

A study was made of the effect of soil and crop type on the soil and total ecosystem respiration rates in agricultural soils in southern Finland. The main interest was to compare the soil respiration rates in peat and two different mineral soils growing barley, grass and potato. Respiration measurements were conducted during the growing season with (1) a closed-dynamic ecosystem respiration chamber, in which combined plant and soil respiration was measured and (2) a closed-dynamic soil respiration chamber which measured only the soil and root-derived respiration. A semi-empirical model including separate functions for the soil and plant respiration components was used for the total ecosystem respiration (TER), and the resulting soil respiration parameters for different soil and crop types were compared. Both methods showed that the soil respiration in the peat soil was 2–3 times as high as that in the mineral soils, varying from 0.11 to 0.36 mg (CO₂) m^–2 s^–1 in the peat soil and from 0.02 to 0.17 mg (CO₂) m^–2 s^–1 in the mineral soils. The difference between the soil types was mainly attributed to the soil organic C content, which in the uppermost 20 cm of the peat soil was 24 kg m^–2, being about 4 times as high as that in the mineral soils. Depending on the measurement method, the soil respiration in the sandy soil was slightly higher than or similar to that in the clay soil. In each soil type, the soil respiration was highest on the grass plots. Higher soil respiration parameter values (R_s0, describing the soil respiration at a soil temperature of 10°C, and obtained by modelling) were found on the barley than on the potato plots. The difference was explained by the different cultivation history of the plots, as the potato plots had lain fallow during the preceding summer. The total ecosystem respiration followed the seasonal evolution in the leaf area and measured photosynthetic flux rates. The 2–3-fold peat soil respiration term as compared to mineral soil indicates that the cultivated peat soil ecosystem is a strong net CO₂ source.     

Spatial and temporal variations of dissolved gases (CH4, CO2, and O2) in peat cores

Spatial and temporal variations in the concentrations of dissolved gases (CH₄, CO₂, and O₂) in peat cores were studied using membrane inlet mass spectrometry (MIMS). Variations in vertical gas profiles were observed between random peat cores taken from hollows on the same peat bog. Methane concentrations in profiles (0–30 cm) generally increased with depth and reached maximum values in the range of 200–450 m CH₄ below about 13-cm depth. In some profiles, a peak of dissolved methane was observed at 7-cm depth. Oxygen penetrated to approximately 2-cm depth in the hollows. The sampling probe was used to continuously monitor CH₄, CO₂, and O₂ concentrations at fixed depths in peat cores over periods of several days. The concentration of dissolved CO₂ and O₂ at 1-cm depth oscillated over a 24-h period with the maximum of CO₂ concentration corresponding with the minimum of 0₂. Diurnal variations in CO₂ but not CH₄ were measured at 15-cm depth; dissolved CO₂ levels decreased during daylight hours to a constant minimum concentration of 4.85 mm. This report also describes the application of MIMS for the measurement of gaseous diffusion rates in peat using an inert gas (argon); the value of D, the diffusion coefficient, was 2.07 × 10^–8 m² s^–1. Correspondence to: D. Lloyd     

Effects of short-term drying and irrigation on CO2 and CH4 production and emission from mesocosms of a northern bog and an alpine fen

Atmospheric CO₂ and CH₄ exchange in peatlands is controlled by water table levels and soil moisture, but impacts of short periods of dryness and rainfall are poorly known. We conducted drying-rewetting experiments with mesocosms from an ombrotrophic northern bog and an alpine, minerotrophic fen. Efflux of CO₂ and CH₄ was measured using static chambers and turnover and diffusion rates were calculated from depth profiles of gas concentrations. Due to a much lower macroporosity in the fen compared to the bog peat, water table fluctuated more strongly when irrigation was stopped and resumed, about 11 cm in the fen and 5 cm in the bog peat. Small changes in air filled porosity caused CO₂ and CH₄ concentrations in the fen peat to be insensitive to changes in water table position. CO₂ emission was by a factor of 5 higher in the fen than in the bog mesocosms and changed little with water table position in both peats. This was probably caused by the importance of the uppermost, permanently unsaturated zone for auto- and heterotrophic CO₂ production, and a decoupling of air filled porosity from water table position. CH₄ emission was <0.4 mmol m^?2 day^?1 in the bog peat, and up to >12.6 mmol m^?2 day^?1 in the fen peat, where it was lowered by water table fluctuations. CH₄ production was limited to the saturated zone in the bog peat but proceeded in the capillary fringe of the fen peat. Water table drawdown partly led to inhibition of methanogenesis in the newly unsaturated zone, but CH₄ production appeared to continue after irrigation without time-lag. The identified effects of irrigation on soil moisture and respiration highlight the importance of peat physical properties for respiratory dynamics; but the atmospheric carbon exchange was fairly insensitive to the small-scale fluctuations induced.     

North American approach to the restoration of Sphagnum dominated peatlands

Sphagnum dominated peatlands do not rehabilitate well after being cutover (mined) for peat and some action needs to be taken in order to restore these sites within a human generation. Peatland restoration is recent and has seen significant advances in the 1990s. A new approach addressing the North American context has been developed and is presentedin this paper. The short-term goal of this approach is to establish a plant cover composed of peat bog species and to restore a water regime characteristic of peatland ecosystems. The long-term objective is to return the cutover areas to functional peat accumulating ecosystems. The approach developed for peatland restoration in North America involves the following steps: 1)field preparation, 2) diaspore collection, 3) diaspore introduction, 4) diaspore protection, and 5) fertilization. Field preparation aims at providing suitable hydrological conditions for diaspores through creation of microtopography and water retention basins, re-shaping cutover fields and blocking ditches. It is site specific because it depends largely onlocal conditions. The second step is the collection of the top 10 centimetres of the living vegetation in a natural bog as a source of diaspores. It is recommended to use a ratio of surface collected to surface restored between 1: 10 and 1: 15 in order to minimize the impact on natural bogs and to insure rapid plant establishment in less than four years. Diaspores are then spread as a thin layer on the bare peat surfaces to be restored. It has been demonstrated that too scant or too thick a layer decreases plant establishment success. Diaspores are then covered by a straw mulch applied at a rate of 3 000 kg ha^-1 which provides improved water availabilityand temperature conditions. Finally, phosphorus fertilization favours more rapid substrate colonization by vascular plants, which have been shown to help stabilize the bare peat surface and act as nurse plants to the Sphagnum mosses.     

Stimulation of both photosynthesis and respiration in response to warmer and drier conditions in a boreal peatland ecosystem

Peatland ecosystems have been consistent carbon (C) sinks for millennia, but it has been predicted that exposure to warmer temperatures and drier conditions associated with climate change will shift the balance between ecosystem photosynthesis and respiration providing a positive feedback to atmospheric CO₂ concentration. Our main objective was to determine the sensitivity of ecosystem photosynthesis, respiration and net ecosystem production (NEP) measured by eddy covariance, to variation in temperature and water table depth associated with interannual shifts in weather during 2004–2009. Our study was conducted in a moderately rich treed fen, the most abundant peatland type in western Canada, in a region (northern Alberta) where peatland ecosystems are a significant landscape component. During the study, the average growing season (May–October) water depth declined approximately 38 cm, and temperature [expressed as cumulative growing degree days (GDD, March–October)] varied approximately 370 GDD. Contrary to previous predictions, both ecosystem photosynthesis and respiration showed similar increases in response to warmer and drier conditions. The ecosystem remained a strong net sink for CO₂ with an average NEP (± SD) of 189 ± 47 g C m^?2 yr^?1. The current net CO₂ uptake rates were much higher than C accumulation in peat determined from analyses of the relationship between peat age and cumulative C stock. The balance between C addition to, and total loss from, the top 0–30 cm depth (peat age range 0–70 years) of shallow peat cores averaged 43 ± 12 g C m^?2 yr^?1. The apparent long‐term average rate of net C accumulation in basal peat samples was 19–24 g C m^?2 yr^?1. The difference between current rates of net C uptake and historical rates of peat accumulation is likely a result of vegetation succession and recent increases in tree establishment and productivity.