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.     

Exchange of CO2, CH4 and N2O between the atmosphere and two northern boreal ponds with catchments dominated by peatlands or forests

Concentrations of carbon dioxide (CO₂), methane (CH₄) and nitrous oxide (N₂O) in the water column and their exchange at the water/air interface were studied during the open water period in two freshwater ponds with different catchment characteristics in the northern boreal zone in Finland; either peatlands or coniferous upland forests dominated the catchment of the ponds. Both ponds were supersaturated with dissolved CO₂ and CH₄ with respect to the equilibrium with the atmosphere, but were close to the equilibrium with N₂O. The mean CO₂ efflux from the pond was higher in the peatland-dominated catchment (22 mg m^–2 h^–1) than in the forested catchment (0.7 mg m^–2 h^–1), whereas the mean CH₄ emissions were similar (7.6 and 3.5 mg m^–2 d^–1, respectively). The fluxes of N₂O were generally negligible. The higher CO₂ concentrations and efflux in the pond with the peatland-dominated catchment were attributed to a greater input of allochthonous carbon to that pond from its catchment due to its higher water colour and higher total organic carbon (TOC) concentration. The water pH, which also differed between the ponds, could additionally affect the CO₂ dynamics. Since the catchment characteristics can regulate aquatic carbon cycles, catchment-scale studies are needed to attain a deeper understanding of the aquatic greenhouse gas dynamics.     

Dynamics of dissolved O2, CO2, CH4, and N2O in a tropical coastal swamp in southern Thailand

We studied the distribution of dissolved O₂, CO₂, CH₄, and N₂O in a coastal swamp system in Thailand with the goal to characterize the dynamics of these gases within the system. The gas concentrations varied spatially and seasonally in both surface and ground waters. The entire system was a strong sourcefor CO₂ and CH₄, and a possible sink for atmospheric N₂O. Seasonal variation in precipitation primarily regulated the redox conditions in the system. However, distributions of CO₂, CH₄, and N₂O in the river that received swamp waters were not always in agreement with redox conditions indicated by dissolvedO₂ concentrations. Sulfate production through pyriteoxidation occurred in the swamp with thin peat layerunder aerobic conditions and was reflected by elevatedSO ₄ ^2– /Cl^– in the river water. When SO ₄ ^2– /Cl^– was high, CO₂ and CH₄ concentrations decreased, whereas the N₂O concentration increased. The excess SO ₄ ^2– in the river water was thus identified as a potential indicator for gas dynamics in this coastal swamp system.     

Soil gas fluxes of N2O,CH4 and CO2 beneath Lolium perenne under elevated CO2: The Swiss free air carbon dioxide enrichment experiment

Fluxes of nitrous oxide, methane and carbon dioxide were measured from soils under ambient (350 µL L^-1) and enhanced (600 µL L^-1) carbon dioxide partial pressures (pCO₂) at the Free Air Carbon Dioxide Enrichment (FACE) experiment, Eidgenössische Technische Hochschule (ETH), Eschikon, Switzerland in July 1995, using a GC housed in a mobile laboratory. Measurements were made in plots of Lolium perenne maintained under high N input. During the data collection period N fertiliser was applied at a rate of 14 g m^-2 of N. Elevated pCO₂ appeared to result in an increased (27%) output of N₂O, thought to be the consequence of enhanced root-derived available soil C, acting as an energy source for denitrification. The climate, agricultural practices and soils at the FACE experiment combined to give rise to some of the largest N₂O emissions recorded for any terrestrial ecosystem. The amount of CO₂–C being lost from the control plot was higher (10%) than for the enhanced CO₂ plot, and is the reverse of that predicted. The control plot oxidised consistently more CH₄ than the enhanced plot, oxidising 25.5 ± 0.8 µg m^-2 hr^-1 of CH₄ for the control plot, with an average of 8.5 ± 0.4 µg m^-2 hr^-1 of CH₄ for the enhanced CO₂ plot. This suggests that elevated pCO₂ may lead to a feedback whereby less CH₄ is removed from the atmosphere. Despite the limited nature of the current study (in time and space), the observations made here on the interactions of elevated pCO₂ and soil trace gas release suggest that significant interactions are occurring. The feedbacks involved could have importance at the global scale.     

Fluxes of CH4 and N2O in aspen stands grown under ambient and twice-ambient CO2

The objectives of this study were: (1) to quantify the effects of plant species' loss from designed calcareous grassland communities at a field site in northwestern Switzerland on the size and composition of earthworm communities, and (2) to evaluate how exposure of plant communities to elevated atmospheric CO2 might alter the effects of plant species' loss on earthworm communities. We non-destructively censused earthworm communities in each of 24 1.2 m2 experimental plots in autumn 1996 when soils were wet and earthworms were active. Each plot contained an experimental plant community with 31, 12 or 5 native plant species (eight plots each). Half of the plots in each species treatment were exposed to ambient CO2 concentrations (350 μL CO2 L-1) and half to elevated CO2 (600 μL CO2 L-1) using screen-aided CO2 control. The study was conducted in the fourth year after community establishment and the third year of CO2 treatment as part of a long-term study on the interactive effects of plant species' loss and elevated CO2 on grassland communities. The size (density and biomass) of earthworm communities declined linearly when the number of plant species in the community was reduced from 31 to 5 species (e.g. 32 ± 1 g m-2 to 23 ± 2 g m-2) due mainly to a decline in the endogeic worm species Allolobophora rosea which was the most abundant of nine earthworm species observed (nearly half of all worms in each plot). However, no changes in the relative contribution of individual species or the three main earthworm ecological groups (anecics, endogeics, epigeics) to the entire earthworm community were observed with declining number of plant species. The responses of earthworm communities to plant species'; loss appear to reflect changes in community fine root biomass in the topsoil (e.g. declining worm biomass with declining fine root biomass) observed in parallel studies conducted at this site. Further the results of this study demonstrate that a loss of plant species from these calcareous grassland communities may also alter the age structure of earthworm communities, but not significantly influence their diversity or composition. Our data also indicate that rising atmospheric CO2 may not greatly impact the size and composition of worm communities or alter the effects of plant species' loss on earthworm communities. Therefore, the disappearance of plant species from these native grasslands, as a result of ever increasing human activities, may be expected to lead to reductions in the size of earthworm communities and the ecosystem services they provide. This revised version was published online in July 2006 with corrections to the Cover Date.     

Evaluation of carbon accrual in afforested agricultural soils

Afforestation of agricultural lands can provide economically and environmentally realistic C storage to mitigate for elevated CO₂ until other actions such as reduced fossil fuel use can be taken. Soil carbon sequestration following afforestation of agricultural land ranges from losses to substantial annual gains. The present understanding of the controlling factors is inadequate for understanding ecosystem dynamics, modeling global change and for policy decision‐makers. Our study found that planting agricultural soils to deciduous forests resulted in ecosystem C accumulations of 2.4 Mg C ha⁻¹ yr⁻¹ and soil accumulations of 0.35 Mg C ha⁻¹ yr⁻¹. Planting to conifers showed an average ecosystem sequestration of 2.5 and 0.26 Mg C ha⁻¹ yr⁻¹ in the soils but showed greater field to field variability than when planted to deciduous forest. Path analysis showed that Ca was positively related to soil C accumulations for both conifers and deciduous afforested sites and played a significant role in soil C accumulations in these sites. Soil N increases were closely related to C accumulation and were two times greater than could be explained by system N inputs from atmospheric deposition and natural sources. Our results suggest that the addition of Ca to afforested sites, especially conifers, may be an economical means to enhance soil C sequestration even if it does not result in increasing C in aboveground pools. The mechanism of N accumulation in these aggrading stands needs further investigation.     

Greenhouse gas dynamics in boreal, littoral sediments under raised CO2 and nitrogen supply

SUMMARY 1. The effects of increasing CO₂ and nitrogen loading and of a change in water table and temperature on littoral CH₄, N₂O and CO₂ fluxes were studied in a glasshouse experiment with intact sediment cores including vegetation (mainly sedges), taken from a boreal eutrophic lake in Finland. Sediments with the water table held at a level of 0 or at ?15 cm were incubated in an atmosphere of 360 or 720 p.p.m. CO₂ for 18 weeks. The experiment included fertilisation with NO₃^– and NH₄⁺ (to a total 3 g N m^?2). 2. Changes in the water table and temperature strongly regulated sediment CH₄ and cCO₂ fluxes (community CO₂ release), but did not affect N₂O emissions. Increase in the water table increased CH₄ emissions but reduced cCO₂ release, while increase in temperature increased emissions of both CO₂ and CH₄. 3. The raised CO₂ increased carbon turnover in the sediments, such that cCO₂ release was increased by 16–26%. However, CH₄ fluxes were not significantly affected by raised CO₂, although CH₄ production potential (at 22 °C) of the sediments incubated at high CO₂ was increased. In the boreal region, littoral CH₄ production is more likely to be limited by temperature than by the availability of carbon. Raised CO₂ did not affect N₂O production by denitrification, indicating that this process was not carbon limited. 4. A low availability of NO₃^– did severely limit N₂O production. The NO₃^– addition caused up to a 100‐fold increase in the fluxes of N₂O. The NH₄⁺ addition did not increase N₂O fluxes, indicating low nitrification capacity in the sediments.     

Characterization of microbial NO production, N2O production and CH4 oxidation initiated by aeration of anoxic rice field soil

Intermittent drainage of rice fields isdiscussed as an option to mitigate emission ofCH₄, an important greenhouse gas. HoweverN₂O, a potentially more effective greenhouse gas,may be emitted during the aeration phase. Therefore,the metabolism of NO, N₂O, NH ,NO and NO and the kinetics ofCH₄ oxidation were measured after aeration ofmethanogenic rice field soil. Before aeration, thesoil contained NH in relatively highconcentrations (about 4 mM), while NO andNO were almost undetectable. Immediatelyafter aeration both NO and N₂O were produced withrates of about 15 pmol h^-1 gdw^-1 and 5 pmolh^-1 gdw^-1, respectively. Simultaneously,NH decreased while NO accumulated. Later on, NO was depletedwhile NO concentrations increased.Characteristic phases of nitrogen turnover wereassociated with the activities of ammonium oxidizers,nitrite oxidizers and denitrifiers. Oxidation ofNH and production of NO and N₂O wereinhibited by 10 Pa acetylene demonstrating thatnitrification was obligatory for the initiation ofnitrogen turnover and production of NO and N₂O.Ammonium oxidation was not limited by the availableNH and thus, concomittant production of NOand N₂O was not stimulated by addition ofNH . However, addition of NO stimulated production of NO and N₂O in bothanoxic and aerated rice soil slurries. In this case,10 Pa acetylene did not inhibit the production of NOand N₂O demonstrating that it was due todenitrification which was obviously limited by theavailability of NO . In the aerated soilslurries CH₄ was only oxidized if present atelevated concentrations >50 ppmv CH₄). Atatmospheric CH₄ concentrations (1.7 ppmv)CH₄ was not consumed, but was even slightly produced.CH₄ oxidation activity increased afterpreincubation at 20% CH₄, and then CH₄was also oxidized at atmospheric concentrations. CH₄oxidation kinetics exhibited sigmoid characteristicsat low CH₄ concentrations presumably because ofinhibition of CH₄ oxidation by NH .     

Soil–atmosphere exchange of CH4, CO,N2O and NOx and the effects of land‐use change in the semiarid Mallee system in Southeastern Australia

The semiarid and arid zones cover a quarter of the global land area and support one‐fifth of the world's human population. A significant fraction of the global soil–atmosphere exchange for climatically active gases occurs in semiarid and arid zones yet little is known about these exchanges. A study was made of the soil–atmosphere exchange of CH₄, CO, N₂O and NO_x in the semiarid Mallee system, in north‐western Victoria, Australia, at two sites: one pristine mallee and the other cleared for approximately 65 years for farming (currently wheat). The mean (± standard error) rates of CH₄ exchange were uptakes of ?3.0 ± 0.5 ng(C) m^?2 s^?1 for the Mallee and ?6.0 ± 0.3 ng(C) m^?2 s^?1 for the Wheat. Converting mallee forest to wheat crop increases CH₄ uptake significantly. CH₄ emissions were observed in the Mallee in summer and were hypothesized to arise from termite activity. We find no evidence that in situ growing wheat plants emit CH₄, contrary to a recent report. The average CO emissions of 10.1 ± 1.8 ng(C) m^?2 s^?1 in the Mallee and 12.6 ± 2.0 ng(C) m^?2 s^?1 in the Wheat. The average N₂O emissions were 0.5 ± 0.1 ng(N) m^?2 s^?1 from the pristine Mallee and 1.4 ± 0.3 ng(N) m^?2 s^?1 from the Wheat. The experimental results show that the processes controlling these exchanges are different to those in temperate systems and are poorly understood.     

Fluxes of nitrous oxide and methane from nitrogen-amended soils in a Colorado alpine ecosystem

In order to determine the effect of increased nitrogen inputs on fluxed of N₂O and CH₄ from alpine soils, we measured fluxes of these gases from fertilized and unfertilized soils in wet and dry alpine meadows. In the dry meadow, the addition of nitrogen resulted in a 22-fold increase in N₂O emissions, while in the wet meadow, we observed a 45-fold increase in N₂O emission rates. CH₄ uptake in the dry meadow was reduced 52% by fertilization; however, net CH₄ production occurred in all the wet meadow plots and emission rates were not significantly affected by fertilization. Net nitrification rates in the dry meadow were higher in fertilized plots than in non-fertilized plots throughout the growing season; net mineralization rates in fertilized dry meadow pots were higher than those in non-fertilized plots during the latter half of the growing season.     

Effect of nitrogen fertilizers and moisture content on CH4 and N2O fluxes in a humisol: Measurements in the field and intact soil cores

Field and laboratory studies were conducted to determine effects of nitrogen fertilizers and soil water content on N₂O and CH₄ fluxes in a humisol located on the Central Experimental Farm of Agriculture Canada, Ottawa. Addition of 100 kg N ha^–1 as either urea or NaNO₃ had no significant effect on soil CH₄ flux measured using chambers. Fertilization with NaNO₃ resulted in a significant but transitory stimulation of N₂O production. Inorganic soil N profiles and the potential nitrification rate suggested that much of the NH ₄ ⁺ from urea hydrolysis was rapidly nitrified. CH₄ fluxes measured using capped soil cores agreed well with fluxes measured using field chambers, and with fluxes calculated from soil gas concentration gradients using Fick's diffusion law. This humisol presents an ideal, unstructured, vertically homogeneous system in which to study gas diffusion, and the influence of gas-filled porosity on CH₄ uptake. In soil cores gradually saturated with H₂O, the relationship of CH₄ flux to gas-filled porosity was an exponential rise to a maximum. Steepening CH₄ concentration gradients partially compensated for the decreasing diffusion coefficient of CH₄ in soil matrix air as water content increased, and diffusion limitation of CH₄ oxidation occurred only at water contents > 130% (dry weight), or gas-filled porosities < 0.2.Corresponding author     

植物对沼泽湿地生态系统CO2和CH4排放的影响

利用静态暗箱/气相色谱法于2003~2005年在生长季对三江平原小叶章(Calamagrostis angustifolia)沼泽化草甸和毛果苔草(Carexlasiocarpa)沼泽地区CO2和CH4的排放通量进行野外对比观测实验。结果表明:2003~2005年生长季小叶章草甸土壤-植物系统CO2排放通量分别是土壤CO2排放通量的1.65、2.06和2.01倍,毛果苔草沼泽土壤-植物系统CO2排放通量分别是土壤CO2排放通量的2.58、2.27和4.21倍,表明沼泽湿地土壤-植物系统CO2排放通量的主要贡献者是植物地上部分的呼吸作用,且3个生长季小叶章草甸CO2排放通量均显著大于毛果苔草沼泽,主要是由于植物生物量的差异以及土壤微生物活性的不同。2003~2005年植物生长季,小叶章草甸土壤-植物系统CH4排放通量分别是土壤的4.84、3.55和6.45倍,毛果苔草沼泽土壤-植物系统CH4排放通量分别是土壤的2.60、1.25和3.22倍,且3个生长季小叶章草甸和毛果苔草沼泽CH4排放通量均具有显著差异,这主要是由于水位的差异以及植物对CH4排放能力的不同造成的。     

Temporal changes in N2O-losses from two arable soils

N₂O-loss rates from two soils were measured over a continuous observation period of 2 years. The two soils, differing in texture (sandy loam and silty loam), are frequently used for intensive crop production. Rates were estimated using a closed soil cover box technique. N₂O-losses obtained were scrutinised with physical, chemical and microbiological properties of the soils as well as with climatic data.Large temporal changes in N₂O-emission rates were found. The data were approximately log-normal distributed. In spring maximal values of 20 g N₂O-N ha^-1 d^-1 were observed. According to this observation, two situations associated with high flux rates could be distinguished; 1. N₂O- production by soil at spring thaw and 2. N₂O-production within one week after N-fertilizer application. For both soils equal N₂O-losses were found, which are adequate to 1 kg N₂O-N ha^-1 per year. From this data was calculated that N₂O-losses ranged from 0.8–1.5% of the applied fertilizer N.     

Ecosystem–atmosphere exchange of CH4 and N2O and ecosystem respiration in wetlands in the Sanjiang Plain, Northeastern China

Natural wetlands are critically important to global change because of their role in modulating atmospheric concentrations of CO₂, CH₄, and N₂O. One 4‐year continuous observation was conducted to examine the exchanges of CH₄ and N₂O between three wetland ecosystems and the atmosphere as well as the ecosystem respiration in the Sanjiang Plain in Northeastern China. From 2002 to 2005, the mean annual budgets of CH₄ and N₂O, and ecosystem respiration were 39.40 ± 6.99 g C m^?2 yr^?1, 0.124 ± 0.05 g N m^?2 yr^?1, and 513.55 ± 8.58 g C m^?2 yr^?1 for permanently inundated wetland; 4.36 ± 1.79 g C m^?2 yr^?1, 0.11 ± 0.12 g N m^?2 yr^?1, and 880.50 ± 71.72 g C m^?2 yr^?1 for seasonally inundated wetland; and 0.21 ± 0.1 g C m^?2 yr^?1, 0.28 ± 0.11 g N m^?2 yr^?1, and 1212.83 ± 191.98 g C m^?2 yr^?1 for shrub swamp. The substantial interannual variation of gas fluxes was due to the significant climatic variability which underscores the importance of long‐term continuous observations. The apparent seasonal pattern of gas emissions associated with a significant relationship of gas fluxes to air temperature implied the potential effect of global warming on greenhouse gas emissions from natural wetlands. The budgets of CH₄ and N₂O fluxes and ecosystem respiration were highly variable among three wetland types, which suggest the uncertainties in previous studies in which all kinds of natural wetlands were treated as one or two functional types. New classification of global natural wetlands in more detailed level is highly expected.     

Management options for reducing CO2 emissions from agricultural soils

Crop-based agriculture occupies 1.7 billion hectares, globally, with a soil C stock of about 170 Pg. Of the past anthropogenic CO² additions to the atmosphere, about 50 Pg C came from the loss of soil organic matter (SOM) in cultivated soils. Improved management practices, however, can rebuild C stocks in agricultural soils and help mitigate CO² emissions.Increasing soil C stocks requires increasing C inputs and/or reducing soil heterotrophic respiration. Management options that contribute to reduced soil respiration include reduced tillage practices (especially no-till) and increased cropping intensity. Physical disturbance associated with intensive soil tillage increases the turnover of soil aggregates and accelerates the decomposition of aggregate-associated SOM. No-till increases aggregate stability and promotes the formation of recalcitrant SOM fractions within stabilized micro- and macroaggregate structures. Experiments using¹³ C natural abundance show up to a two-fold increase in mean residence time of SOM under no-till vs intensive tillage. Greater cropping intensity, i.e., by reducing the frequency of bare fallow in crop rotations and increasing the use of perennial vegetation, can increase water and nutrient use efficiency by plants, thereby increasing C inputs to soil and reducing organic matter decomposition rates.Management and policies to sequester C in soils need to consider that: soils have a finite capacity to store C, gains in soil C can be reversed if proper management is not maintained, and fossil fuel inputs for different management practices need to be factored into a total agricultural CO² balance.     

Response of tundra CH4 and CO2 flux tomanipulation of temperature and vegetation

We conducted plant species removals, air temperaturemanipulations, and vegetation and soil transplants inAlaskan wet-meadow and tussock tundra communities todetermine the relative importance of vegetation typeand environmental variables in controlling ecosystemmethane (CH₄) and carbon dioxide (CO₂) flux. Plastic greenhouses placed over wet-meadow tundraincreased air temperature, soil temperature, and soilmoisture, but did not affect CH₄ or CO₂ flux(measured in the dark). By contrast, removal ofsedges in the wet meadow significantly decreased fluxof CH₄, while moss removal tended to increaseCH₄ emissions. At 15 cm depth, pore-waterCH₄ concentrations were higher in sedge-removalthan in control plots, suggesting that sedgescontribute to CH₄ emissions by transportingCH₄ from anaerobic soil to the atmosphere, ratherthan by promoting methanogenesis. Inreciprocal-ecosystem transplants between thewet-meadow and tussock tundra communities, CH₄and CO₂ emissions were higher overall in thewet-meadow site, but were unrelated to transplantorigin. Methane flux was correlated with localvariation in soil temperature, thaw depth, andwater-table depth, but the relative importance ofthese factors varied through the season. Our resultssuggest that future changes in CH₄ and CO₂flux in response to climatic change will be morestrongly mediated by large-scale changes in vegetationand soil parameters than by direct temperature effects.     

Nitrate limitation of N2O production and denitrification from tropical pasture and rain forest soils

Nitrous oxide production was measured in intact cores taken from active pasture and old-growth forest Inceptisols in the Atlantic Lowlands of Costa Rica. Following additions of aqueous KNO₃ or glucose, or the two combined amendments, the cores were incubated in the laboratory to determine if N₂O production rates were either N-limited or C-limited in the two land use types. Differences in rates of denitrification (N2₂O + N₂ production) among amended forest and pasture soils were determined by addition of 10% C₂H₂.The forest soils were relatively insensitive to all amendment additions, including the acetylene block. Forest N₂O production rates among the treatments did not differ from the controls, and were consistently lower than those of the pasture soils. With the addition of glucose plus nitrate to the forest soils, production of N₂O was three times greater than the controls, although this increase was not statistically significant. On the other hand, the pasture soils were definitely nitrogen-limited since N₂O production rates were increased substantially beyond controls by all the amendments which contained nitrate, despite the very low N level (5 mg N kg^–1 soil) relative to typical fertilizer applications. With respect to the nitrate plus glucose plus acetylene treatment, denitrification was high in the pasture soils; N₂O production in the presence of C₂H₂ was 150% of the rate of N₂O production measured in the absence of the acetylene block. The results are discussed in relation to the effects of agricultural land use practices and subsequent impacts of disturbance on N₂O release.     

Enhanced CH4 emission from a wetland soil exposed to Elevated CO2

Methane emissions from wetland soils are generally a positive function ofplant size and primary productivity, and may be expected to increase dueto enhanced rates of plant growth in a future atmosphere of elevatedCO₂. We performed two experiments with Orontium aquaticum, acommon emergent aquatic macrophyte in temperate and sub-tropical wetlands, todetermine if enhanced rates of photosynthesis in elevated CO₂atmospheres would increase CH₄ emissions from wetland soils.O. aquaticum was grown from seed in soil cores under ambient and elevated(ca. 2-times ambient) concentrations of CO₂ in an initialglasshouse study lasting 3 months and then a growth chamber study lasting 6months. Photosynthetic rates were 54 to 71% higher underelevated CO₂ than ambient CO₂, but plantbiomass was not significantly different at the end of the experiment. Ineach case, CH₄ emissions were higher under elevated thanambient CO₂ levels after 2 to 4 months of treatment, suggestinga close coupling between photosynthesis and methanogenesis in our plant-soilsystem. Methane emissions in the growth chamber study increased by 136%. We observed a significant decrease in transpirationrates under elevated CO₂ in the growth chamber study, andspeculate that elevated CO₂ may also stimulate CH₄ emissions by increasing the extent and duration offlooding in some wetland ecosystems. Elevated CO₂ maydramatically increase CH₄ emissions from wetlands, a sourcethat currently accounts for 40% of global emissions.     

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.