Environmental factors controlling temporal and spatial variability in the soil‐atmosphere exchange of CO2, CH4 and N2O from an Australian subtropical rainforest

The temporal variations in CO₂, CH₄ and N₂O fluxes were measured over two consecutive years from February 2007 to March 2009 from a subtropical rainforest in south‐eastern Queensland, Australia, using an automated sampling system. A concurrent study using an additional 30 manual chambers examined the spatial variability of emissions distributed across three nearby remnant rainforest sites with similar vegetation and climatic conditions. Interannual variation in fluxes of all gases over the 2 years was minimal, despite large discrepancies in rainfall, whereas a pronounced seasonal variation could only be observed for CO₂ fluxes. High infiltration, drainage and subsequent high soil aeration under the rainforest limited N₂O loss while promoting substantial CH₄ uptake. The average annual N₂O loss of 0.5 ± 0.1 kg N₂O‐N ha^?1 over the 2‐year measurement period was at the lower end of reported fluxes from rainforest soils. The rainforest soil functioned as a sink for atmospheric CH₄ throughout the entire 2‐year period, despite periods of substantial rainfall. A clear linear correlation between soil moisture and CH₄ uptake was found. Rates of uptake ranged from greater than 15 g CH₄‐C ha^?1 day^?1 during extended dry periods to less than 2–5 g CH₄‐C ha^?1 day^?1 when soil water content was high. The calculated annual CH₄ uptake at the site was 3.65 kg CH₄‐C ha^?1 yr^?1. This is amongst the highest reported for rainforest systems, reiterating the ability of aerated subtropical rainforests to act as substantial sinks of CH₄. The spatial study showed N₂O fluxes almost eight times higher, and CH₄ uptake reduced by over one‐third, as clay content of the rainforest soil increased from 12% to more than 23%. This demonstrates that for some rainforest ecosystems, soil texture and related water infiltration and drainage capacity constraints may play a more important role in controlling fluxes than either vegetation or seasonal variability.     

Predicting long‐term carbon mineralization and trace gas production from thawing permafrost of Northeast Siberia

The currently observed Arctic warming will increase permafrost degradation followed by mineralization of formerly frozen organic matter to carbon dioxide (CO₂) and methane (CH₄). Despite increasing awareness of permafrost carbon vulnerability, the potential long‐term formation of trace gases from thawing permafrost remains unclear. The objective of the current study is to quantify the potential long‐term release of trace gases from permafrost organic matter. Therefore, Holocene and Pleistocene permafrost deposits were sampled in the Lena River Delta, Northeast Siberia. The sampled permafrost contained between 0.6% and 12.4% organic carbon. CO₂ and CH₄ production was measured for 1200 days in aerobic and anaerobic incubations at 4 °C. The derived fluxes were used to estimate parameters of a two pool carbon degradation model. Total CO₂ production was similar in Holocene permafrost (1.3 ± 0.8 mg CO₂‐C gdw^?1 aerobically, 0.25 ± 0.13 mg CO₂‐C gdw^?1 anaerobically) as in 34 000–42 000‐year‐old Pleistocene permafrost (1.6 ± 1.2 mg CO₂‐C gdw^?1 aerobically, 0.26 ± 0.10 mg CO₂‐C gdw^?1 anaerobically). The main predictor for carbon mineralization was the content of organic matter. Anaerobic conditions strongly reduced carbon mineralization since only 25% of aerobically mineralized carbon was released as CO₂ and CH₄ in the absence of oxygen. CH₄ production was low or absent in most of the Pleistocene permafrost and always started after a significant delay. After 1200 days on average 3.1% of initial carbon was mineralized to CO₂ under aerobic conditions while without oxygen 0.55% were released as CO₂ and 0.28% as CH₄. The calibrated carbon degradation model predicted cumulative CO₂ production over a period of 100 years accounting for 15.1% (aerobic) and 1.8% (anaerobic) of initial organic carbon, which is significantly less than recent estimates. The multiyear time series from the incubation experiments helps to more reliably constrain projections of future trace gas fluxes from thawing permafrost landscapes.     

Methane flux dynamics in an Irish lowland blanket bog

Pristine peatlands are a significant source of atmospheric methane (CH₄). Large spatio–temporal variation has been observed in flux rates within and between peatlands. Variation is commonly associated with water level, vegetation structure, soil chemistry and climatic variability. We measured spatial and temporal variation in CH₄ fluxes in a blanket bog during the period 2003–2005. The surface of the bog was composed of different vegetation communities (hummocks, lawns and hollows) along a water level gradient. CH₄ fluxes were measured in each community using a chamber method. Regression modelling was used to relate the fluxes with environmental variables and to integrate fluxes over the study period. Water level was the strongest controller of spatial variation; the average flux rate was lowest in hummocks and highest in hollows, ranging from 3 to 53 mg CH₄ m⁻² day⁻¹. In vegetation communities with a permanently high water level, the amount and species composition of vegetation was also a good indicator of flux rate. We observed a clear seasonal variation in flux that was chiefly controlled by temperature. The annual average flux (6.2 g CH₄ m⁻² year⁻¹) was similar to previous estimates from blanket bogs and continental raised bogs. No interannual variation was observed.     

Carbon balance of rewetted and drained peat soils used for biomass production: a mesocosm study

Rewetting of drained peatlands has been recommended to reduce CO₂ emissions and to restore the carbon sink function of peatlands. Recently, the combination of rewetting and biomass production (paludiculture) has gained interest as a possible land use option in peatlands for obtaining such benefits of lower CO₂ emissions without losing agricultural land. This study quantified the carbon balance (CO₂, CH₄ and harvested biomass C) of rewetted and drained peat soils under intensively managed reed canary grass (RCG) cultivation. Mesocosms were maintained at five different groundwater levels (GWLs), that is 0, 10, 20 cm below the soil surface, representing rewetted peat soils, and 30 and 40 cm below the soil surface, representing drained peat soils. Net ecosystem exchange (NEE) of CO₂ and CH₄ emissions was measured during the growing period of RCG (May to September) using transparent and opaque closed chamber methods. The average dry biomass yield was significantly lower from rewetted peat soils (12 Mg ha^?1) than drained peat soils (15 Mg ha^?1). Also, CO₂ fluxes of gross primary production (GPP) and ecosystem respiration (ER) from rewetted peat soils were significantly lower than from drained peat soils, but net uptake of CO₂ was higher from rewetted peat soils. Cumulative CH₄ emissions were negligible (0.01 g CH₄ m^?2) from drained peat soils but were significantly higher (4.9 g CH₄ m^?2) from rewetted peat soils during measurement period (01 May–15 September 2013). The extrapolated annual C balance was 0.03 and 0.68 kg C m^?2 from rewetted and drained peat soils, respectively, indicating that rewetting and paludiculture can reduce the loss of carbon from peatlands.     

Effects of seasonality,transport pathway,and spatial structure on greenhouse gas fluxes in a restored wetland

Wetlands can influence global climate via greenhouse gas (GHG) exchange of carbon dioxide (CO₂), methane (CH₄), and nitrous oxide (N₂O). Few studies have quantified the full GHG budget of wetlands due to the high spatial and temporal variability of fluxes. We report annual open‐water diffusion and ebullition fluxes of CO₂, CH₄, and N₂O from a restored emergent marsh ecosystem. We combined these data with concurrent eddy‐covariance measurements of whole‐ecosystem CO₂ and CH₄ exchange to estimate GHG fluxes and associated radiative forcing effects for the whole wetland, and separately for open‐water and vegetated cover types. Annual open‐water CO₂, CH₄, and N₂O emissions were 915 ± 95 g C‐CO₂ m^?2 yr^?1, 2.9 ± 0.5 g C‐CH₄ m^?2 yr^?1, and 62 ± 17 mg N‐N₂O m^?2 yr^?1, respectively. Diffusion dominated open‐water GHG transport, accounting for >99% of CO₂ and N₂O emissions, and ~71% of CH₄ emissions. Seasonality was minor for CO₂ emissions, whereas CH₄ and N₂O fluxes displayed strong and asynchronous seasonal dynamics. Notably, the overall radiative forcing of open‐water fluxes (3.5 ± 0.3 kg CO₂‐eq m^?2 yr^?1) exceeded that of vegetated zones (1.4 ± 0.4 kg CO₂‐eq m^?2 yr^?1) due to high ecosystem respiration. After scaling results to the entire wetland using object‐based cover classification of remote sensing imagery, net uptake of CO₂ (?1.4 ± 0.6 kt CO₂‐eq yr^?1) did not offset CH₄ emission (3.7 ± 0.03 kt CO₂‐eq yr^?1), producing an overall positive radiative forcing effect of 2.4 ± 0.3 kt CO₂‐eq yr^?1. These results demonstrate clear effects of seasonality, spatial structure, and transport pathway on the magnitude and composition of wetland GHG emissions, and the efficacy of multiscale flux measurement to overcome challenges of wetland heterogeneity.     

Spatial variation in landscape‐level CO2 and CH4 fluxes from arctic coastal tundra: influence from vegetation,wetness, and the thaw lake cycle

Regional quantification of arctic CO₂ and CH₄ fluxes remains difficult due to high landscape heterogeneity coupled with a sparse measurement network. Most of the arctic coastal tundra near Barrow, Alaska is part of the thaw lake cycle, which includes current thaw lakes and a 5500‐year chronosequence of vegetated thaw lake basins. However, spatial variability in carbon fluxes from these features remains grossly understudied. Here, we present an analysis of whole‐ecosystem CO₂ and CH₄ fluxes from 20 thaw lake cycle features during the 2011 growing season. We found that the thaw lake cycle was largely responsible for spatial variation in CO₂ flux, mostly due to its control on gross primary productivity (GPP). Current lakes were significant CO₂ sources that varied little. Vegetated basins showed declining GPP and CO₂ sink with age (R² = 67% and 57%, respectively). CH₄ fluxes measured from a subset of 12 vegetated basins showed no relationship with age or CO₂ flux components. Instead, higher CH₄ fluxes were related to greater landscape wetness (R² = 57%) and thaw depth (additional R² = 28%). Spatial variation in CO₂ and CH₄ fluxes had good satellite remote sensing indicators, and we estimated the region to be a small CO₂ sink of ?4.9 ± 2.4 (SE) g C m^?2 between 11 June and 25 August, which was countered by a CH₄ source of 2.1 ± 0.2 (SE) g C m^?2. Results from our scaling exercise showed that developing or validating regional estimates based on single tower sites can result in significant bias, on average by a factor 4 for CO₂ flux and 30% for CH₄ flux. Although our results are specific to the Arctic Coastal Plain of Alaska, the degree of landscape‐scale variability, large‐scale controls on carbon exchange, and implications for regional estimation seen here likely have wide relevance to other arctic landscapes.     

Large‐scale patterns in summer diffusive CH4 fluxes across boreal lakes,and contribution to diffusive C emissions

Lakes are a major component of boreal landscapes, and whereas lake CO₂ emissions are recognized as a major component of regional C budgets, there is still much uncertainty associated to lake CH₄ fluxes. Here, we present a large‐scale study of the magnitude and regulation of boreal lake summer diffusive CH₄ fluxes, and their contribution to total lake carbon (C) emissions, based on in situ measurements of concentration and fluxes of CH₄ and CO₂ in 224 lakes across a wide range of lake type and environmental gradients in Québec. The diffusive CH₄ flux was highly variable (mean 11.6 ± 26.4 SD mg m^?2 d^?1), and it was positively correlated with temperature and lake nutrient status, and negatively correlated with lake area and colored dissolved organic matter (CDOM). The relationship between CH₄ and CO₂ concentrations fluxes was weak, suggesting major differences in their respective sources and/or regulation. For example, increasing water temperature leads to higher CH₄ flux but does not significantly affect CO₂ flux, whereas increasing CDOM concentration leads to higher CO₂ flux but lower CH₄ flux. CH₄ contributed to 8 ± 23% to the total lake C emissions (CH₄ + CO₂), but 18 ± 25% to the total flux in terms of atmospheric warming potential, expressed as CO₂‐equivalents. The incorporation of ebullition and plant‐mediated CH₄ fluxes would further increase the importance of lake CH₄. The average Q₁₀ of CH₄ flux was 3.7, once other covarying factors were accounted for, but this apparent Q₁₀ varied with lake morphometry and was higher for shallow lakes. We conclude that global climate change and the resulting shifts in temperature will strongly influence lake CH₄ fluxes across the boreal biome, but these climate effects may be altered by regional patterns in lake morphometry, nutrient status, and browning.     

Carbon dioxide,methane, and nitrous oxide exchanges in an age‐sequence of temperate pine forests

We investigated soil carbon dioxide (CO₂), methane (CH₄), and nitrous oxide (N₂O) exchanges in an age‐sequence (4, 17, 32, 67 years old) of eastern white pine (Pinus strobus L.) forests in southern Ontario, Canada, for the period of mid‐April to mid‐December in 2006 and 2007. For both CH₄ and N₂O, we observed uptake and emission ranging from ?160 to 245 μg CH₄ m^?2 h^?1 and ?52 to 21 μg N₂O m^?2 h^?1, respectively (negative values indicate uptake). Mean fluxes from mid‐April to mid‐December across the 4, 17, 32, 67 years old stands were similar for CO₂ fluxes (259, 246, 220, and 250 mg CO₂ m^?2 h^?1, respectively), without pattern for N₂O fluxes (?3.7, 1.5, ?2.2, and ?7.6 μg N₂O m^?2 h^?1, respectively), whereas the uptake rates of CH₄ increased with stand age (6.4, ?7.9, ?10.8, and ?23.3 μg CH₄ m^?2 h^?1, respectively). For the same period, the combined contribution of CH₄ and N₂O exchanges to the global warming potential (GWP) calculated from net ecosystem exchange of CO₂ and aggregated soil exchanges of CH₄ and N₂O was on average 4%, <1%, <1%, and 2% for the 4, 17, 32, 67 years old stand, respectively. Soil CO₂ fluxes correlated positively with soil temperature but had no relationship with soil moisture. We found no control of soil temperature or soil moisture on CH₄ and N₂O fluxes, but CH₄ emission was observed following summer rainfall events. LFH layer removal reduced CO₂ emissions by 43%, increased CH₄ uptake during dry and warm soil conditions by more than twofold, but did not affect N₂O flux. We suggest that significant alternating sink and source potentials for both CH₄ and N₂O may occur in N‐ and soil water‐limited forest ecosystems, which constitute a large portion of forest cover in temperate areas.     

Soil‐derived trace gas fluxes from different energy crops – results from a field experiment in Southwest Germany

Willow coppice, energy maize and Miscanthus were evaluated regarding their soil‐derived trace gas emission potential involving a nonfertilized and a crop‐adapted slow‐release nitrogen (N) fertilizer scheme. The N application rate was 80 kg N ha^?1 yr^?1 for the perennial crops and 240 kg N ha^?1 yr^?1 for the annual maize. A replicated field experiment was conducted with 1‐year measurements of soil fluxes of CH₄, CO₂ and N₂O in weekly intervals using static chambers. The measurements revealed a clear seasonal trend in soil CO₂ emissions, with highest emissions being found for the N‐fertilized Miscanthus plots (annual mean: 50 mg C m^?² h^?1). Significant differences between the cropping systems were found in soil N₂O emissions due to their dependency on amount and timing of N fertilization. N‐fertilized maize plots had highest N₂O emissions by far, which accumulated to 3.6 kg N₂O ha^?1 yr^?1. The contribution of CH₄ fluxes to the total soil greenhouse gas subsumption was very small compared with N₂O and CO₂. CH₄ fluxes were mostly negative indicating that the investigated soils mainly acted as weak sinks for atmospheric CH₄. To identify the system providing the best ratio of yield to soil N₂O emissions, a subsumption relative to biomass yields was calculated. N‐fertilized maize caused the highest soil N₂O emissions relative to dry matter yields. Moreover, unfertilized maize had higher relative soil N₂O emissions than unfertilized Miscanthus and willow. These results favour perennial crops for bioenergy production, as they are able to provide high yields with low N₂O emissions in the field.     

Long‐term nutrient addition increases respiration and nitrous oxide emissions in a New England salt marsh

Salt marshes may act either as greenhouse gas (GHG) sources or sinks depending on hydrological conditions, vegetation communities, and nutrient availability. In recent decades, eutrophication has emerged as a major driver of change in salt marsh ecosystems. An ongoing fertilization experiment at the Great Sippewissett Marsh (Cape Cod, USA) allows for observation of the results of over four decades of nutrient addition. Here, nutrient enrichment stimulated changes to vegetation communities that, over time, have resulted in increased elevation of the marsh platform. In this study, we measured fluxes of carbon dioxide (CO₂), methane (CH₄) and nitrous oxide (N₂O) in dominant vegetation zones along elevation gradients of chronically fertilized (1,572 kg N ha^?1 year^?1) and unfertilized (12 kg N ha^?1 year^?1) experimental plots at Great Sippewissett Marsh. Flux measurements were performed using darkened chambers to focus on community respiration and excluded photosynthetic CO₂ uptake. We hypothesized that N‐replete conditions in fertilized plots would result in larger N₂O emissions relative to control plots and that higher elevations caused by nutrient enrichment would support increased CO₂ and N₂O and decreased CH₄ emissions due to the potential for more oxygen diffusion into sediment. Patterns of GHG emission supported our hypotheses. Fertilized plots were substantially larger sources of N₂O and had higher community respiration rates relative to control plots, due to large emissions of these GHGs at higher elevations. While CH₄ emissions displayed a negative relationship with elevation, they were generally small across elevation gradients and nutrient enrichment treatments. Our results demonstrate that at decadal scales, vegetation community shifts and associated elevation changes driven by chronic eutrophication affect GHG emission from salt marshes. Results demonstrate the necessity of long‐term fertilization experiments to understand impacts of eutrophication on ecosystem function and have implications for how chronic eutrophication may impact the role that salt marshes play in sequestering C and N.     

Greenhouse gas fluxes from tropical peatlands in south‐east Asia

The lowland peatlands of south‐east Asia represent an immense reservoir of fossil carbon and are reportedly responsible for 30% of the global carbon dioxide (CO₂) emissions from Land Use, Land Use Change and Forestry. This paper provides a review and meta‐analysis of available literature on greenhouse gas fluxes from tropical peat soils in south‐east Asia. As in other parts of the world, water level is the main control on greenhouse gas fluxes from south‐east Asian peat soils. Based on subsidence data we calculate emissions of at least 900 g CO₂ m^?2 a^?1 (～250 g C m^?2 a^?1) for each 10 cm of additional drainage depth. This is a conservative estimate as the role of oxidation in subsidence and the increased bulk density of the uppermost drained peat layers are yet insufficiently quantified. The majority of published CO₂ flux measurements from south‐east Asian peat soils concerns undifferentiated respiration at floor level, providing inadequate insight on the peat carbon balance. In contrast to previous assumptions, regular peat oxidation after drainage might contribute more to the regional long‐term annual CO₂ emissions than peat fires. Methane fluxes are negligible at low water levels and amount to up to 3 mg CH₄ m^?2 h^?1 at high water levels, which is low compared with emissions from boreal and temperate peatlands. The latter emissions may be exceeded by fluxes from rice paddies on tropical peat soil, however. N₂O fluxes are erratic with extremely high values upon application of fertilizer to wet peat soils. Current data on CO₂ and CH₄ fluxes indicate that peatland rewetting in south‐east Asia will lead to substantial reductions of net greenhouse gas emissions. There is, however, an urgent need for further quantitative research on carbon exchange to support the development of consistent policies for climate change mitigation.     

Winter precipitation and snow accumulation drive the methane sink or source strength of Arctic tussock tundra

Arctic winter precipitation is projected to increase with global warming, but some areas will experience decreases in snow accumulation. Although Arctic CH₄ emissions may represent a significant climate forcing feedback, long‐term impacts of changes in snow accumulation on CH₄ fluxes remain uncertain. We measured ecosystem CH₄ fluxes and soil CH₄ and CO₂ concentrations and ¹³C composition to investigate the metabolic pathways and transport mechanisms driving moist acidic tundra CH₄ flux over the growing season (Jun–Aug) after 18 years of experimental snow depth increases and decreases. Deeper snow increased soil wetness and warming, reducing soil %O₂ levels and increasing thaw depth. Soil moisture, through changes in soil %O₂ saturation, determined predominance of methanotrophy or methanogenesis, with soil temperature regulating the ecosystem CH₄ sink or source strength. Reduced snow (RS) increased the fraction of oxidized CH₄ (Fox) by 75–120% compared to Ambient, switching the system from a small source to a net CH₄ sink (21 ± 2 and ?31 ± 1 mg CH₄ m^?2 season^?1 at Ambient and RS). Deeper snow reduced Fox by 35–40% and 90–100% in medium‐ (MS) and high‐ (HS) snow additions relative to Ambient, contributing to increasing the CH₄ source strength of moist acidic tundra (464 ± 15 and 3561 ± 97 mg CH₄ m^?2 season^?1 at MS and HS). Decreases in Fox with deeper snow were partly due to increases in plant‐mediated CH₄ transport associated with the expansion of tall graminoids. Deeper snow enhanced CH₄ production within newly thawed soils, responding mainly to soil warming rather than to increases in acetate fermentation expected from thaw‐induced increases in SOC availability. Our results suggest that increased winter precipitation will increase the CH₄ source strength of Arctic tundra, but the resulting positive feedback on climate change will depend on the balance between areas with more or less snow accumulation than they are currently facing.     

Initial nitrous oxide,carbon dioxide,and methane costs of converting conservation reserve program grassland to row crops under no‐till vs. conventional tillage

Around 4.4 million ha of land in USDA Conservation Reserve Program (CRP) contracts will expire between 2013 and 2018 and some will likely return to crop production. No‐till (NT) management offers the potential to reduce the global warming costs of CO₂, CH₄, and N₂O emissions during CRP conversion, but to date there have been no CRP conversion tillage comparisons. In 2009, we converted portions of three 9–21 ha CRP fields in Michigan to conventional tillage (CT) or NT soybean production and reserved a fourth field for reference. Both CO₂ and N₂O fluxes increased following herbicide application in all converted fields, but in the CT treatment substantial and immediate N₂O and CO₂ fluxes occurred after tillage. For the initial 201‐day conversion period, average daily N₂O fluxes (g N₂O‐N ha^?1 d^?1) were significantly different in the order: CT (47.5 ± 6.31, n = 6) ? NT (16.7 ± 2.45, n = 6) ? reference (2.51 ± 0.73, n = 4). Similarly, soil CO₂ fluxes in CT were 1.2 times those in NT and 3.1 times those in the unconverted CRP reference field. All treatments were minor sinks for CH₄ (?0.69 ± 0.42 to ?1.86 ± 0.37 g CH₄–C ha^?1 d^?1) with no significant differences among treatments. The positive global warming impact (GWI) of converted soybean fields under both CT (11.5 Mg CO₂e ha^?1) and NT (2.87 Mg CO₂e ha^?1) was in contrast to the negative GWI of the unconverted reference field (?3.5 Mg CO₂e ha^?1) with on‐going greenhouse gas (GHG) mitigation. N₂O contributed 39.3% and 55.0% of the GWI under CT and NT systems with the remainder contributed by CO₂ (60.7% and 45.0%, respectively). Including foregone mitigation, we conclude that NT management can reduce GHG costs by ~60% compared to CT during initial CRP conversion.     

Greenhouse gas emissions from the energy crop oilseed rape (Brassica napus); the role of photosynthetically active radiation in diurnal N2O flux variation

Oilseed rape (OSR, Brassica napus L.) is an important feedstock for biodiesel; hence, carbon dioxide (CO₂), methane (CH₄) and particularly fertilizer‐derived nitrous oxide (N₂O) emissions during cultivation must be quantified to assess putative greenhouse gas (GHG) savings, thus creating an urgent and increasing need for such data. Substrates of nitrification [ammonium (NH₄)] and denitrification [nitrate (NO₃)], the predominant N₂O production pathways, were supplied separately and in combination to OSR in a UK field trial aiming to: (i) produce an accurate GHG budget of fertilizer application; (ii) characterize short‐ to medium‐term variation in GHG fluxes; (iii) establish the processes driving N₂O emission. Three treatments were applied twice, 1 week apart: ammonium nitrate fertilizer (NH₄NO₃, 69 kg‐N ha^?1) mimicking the farm management, ammonium chloride (NH₄Cl, 34.4 kg‐N ha^?1) and sodium nitrate (NaNO₃, 34.6 kg‐N ha^?1). We deployed SkyLine2D for the very first time, a novel automated chamber system to measure CO_2, CH₄ and N₂O fluxes at unprecedented high temporal and spatial resolution from OSR. During 3 weeks following the fertilizer application, CH₄ fluxes were negligible, but all treatments were a net sink for CO₂ (ca. 100 g CO₂ m^?2). Cumulative N₂O emissions (ca. 120 g CO₂‐eq m^?2) from NH₄NO₃ were significantly greater (P < 0.04) than from NaNO₃ (ca. 80 g CO₂‐eq m^?2), but did not differ from NH₄Cl (ca. 100 g CO₂‐eq m^?2) and reduced the carbon sink of photosynthesis so that OSR was a net GHG source in the fertilizer treatment. Diurnal variation in N₂O emissions, peaking in the afternoon, was more strongly associated with photosynthetically active radiation (PAR) than temperature. This suggests that the supply of carbon (C) from photosynthate may have been the key driver of the observed diurnal pattern in N₂O emission and thus should be considered in future process‐based models of GHG emissions.     

Release of CO2 and CH4 from lakes and drainage ditches in temperate wetlands

Shallow fresh water bodies in peat areas are important contributors to greenhouse gas fluxes to the atmosphere. In this study we determined the magnitude of CH₄ and CO₂ fluxes from 12 water bodies in Dutch wetlands during the summer season and studied the factors that might regulate emissions of CH₄ and CO₂ from these lakes and ditches. The lakes and ditches acted as CO₂ and CH₄ sources of emissions to the atmosphere; the fluxes from the ditches were significantly larger than the fluxes from the lakes. The mean greenhouse gas flux from ditches and lakes amounted to 129.1 ± 8.2 (mean ± SE) and 61.5 ± 7.1 mg m^?2 h^?1 for CO₂ and 33.7 ± 9.3 and 3.9 ± 1.6 mg m^?2 h^?1 for CH₄, respectively. In most water bodies CH₄ was the dominant greenhouse gas in terms of warming potential. Trophic status of the water and the sediment was an important factor regulating emissions. By using multiple linear regression 87% of the variation in CH₄ could be explained by PO₄ ^3? concentration in the sediment and Fe²⁺ concentration in the water, and 89% of the CO₂ flux could be explained by depth, EC and pH of the water. Decreasing the nutrient loads and input of organic substrates to ditches and lakes by for example reducing application of fertilizers and manure within the catchments and decreasing upward seepage of nutrient rich water from the surrounding area will likely reduce summer emissions of CO₂ and CH₄ from these water bodies.     

N2O and CH4 fluxes in undisturbed and burned holm oak, scots pine and pyrenean oak forests in central Spain

We investigated N₂O and CH₄ fluxes from soils of Quercus ilex, Quercus pyrenaica and Pinus sylvestris stands located in the surrounding area of Madrid (Spain). The fluxes were measured for 18?months from both mature stands and post fire stands using the static chamber technique. Simultaneously with gas fluxes, soil temperature, soil water content, soil C and soil N were measured in the stands. Nitrous oxide fluxes ranged from ?11.43 to 8.34?μg N₂O–N?m^?2?h^?1 in Q.ilex, ?7.74 to 13.52?μg N₂O–N?m^?2?h^?1 in Q. pyrenaica and ?28.17 to 21.89?μg N₂O–N?m^?2?h^?1 in P. sylvestris. Fluxes of CH₄ ranged from ?8.12 to 4.11?μg CH₄–C?m^?2?h^?1 in Q.ilex, ?7.74 to 3.0?μg CH₄–C m^?2?h^?1 in Q. pyrenaica and ?24.46 to 6.07?μg CH₄–C?m^?2?h^?1 in P. sylvestris. Seasonal differences were detected; N₂O fluxes being higher in wet months whereas N₂O fluxes declined in dry months. Net consumption of N₂O was related to low N availability, high soil C contents, high soil temperatures and low moisture content. Fire decreased N₂O fluxes in spring. N₂O emissions were closely correlated with previous day’s rainfall and soil moisture. Our ecosystems generally were a sink for methane in the dry season and a source of CH₄ during wet months. The available water in the soil influenced the observed seasonal trend. The burned sites showed higher CH₄ oxidation rates in Q. ilex, and lower rates in P. sylvestris. Overall, the data suggest that fire alters both N₂O and CH₄ fluxes. However, the magnitude of such variation depends on the site, soil characteristics and seasonal climatic conditions.     

Full carbon and greenhouse gas balances of fertilized and nonfertilized reed canary grass cultivations on an abandoned peat extraction area in a dry year

Bioenergy crop cultivation on former peat extraction areas is a potential after‐use option that provides a source of renewable energy while mitigating climate change through enhanced carbon (C) sequestration. This study investigated the full C and greenhouse gas (GHG) balances of fertilized (RCG‐F) and nonfertilized (RCG‐C) reed canary grass (RCG; Phalaris arundinacea) cultivation compared to bare peat (BP) soil within an abandoned peat extraction area in western Estonia during a dry year. Vegetation sampling, static chamber and lysimeter measurements were carried out to estimate above‐ and belowground biomass production and allocation, fluxes of carbon dioxide (CO₂), methane (CH₄) and nitrous oxide (N₂O) in cultivated strips and drainage ditches as well as the dissolved organic carbon (DOC) export, respectively. Heterotrophic respiration was determined from vegetation‐free trenched plots. Fertilization increased the above‐ to belowground biomass production ratio and the autotrophic to heterotrophic respiration ratio. The full C balance (incl. CO₂, CH₄ and DOC fluxes from strips and ditches) was 96, 215 and 180 g C m^?2 yr^?1 in RCG‐F, RCG‐C and BP, respectively, suggesting that all treatments acted as C sources during the dry year. The C balance was driven by variations in the net CO₂ exchange, whereas the combined contribution of CH₄ and DOC fluxes was <5%. The GHG balances were 3.6, 7.9 and 6.6 t CO₂ eq ha^?1 yr^?1 in RCG‐F, RCG‐C and BP, respectively. The CO₂ exchange was also the dominant component of the GHG balance, while the contributions of CH₄ and N₂O were <1% and 1–6%, respectively. Overall, this study suggests that maximizing plant growth and the associated CO₂ uptake through adequate water and nutrient supply is a key prerequisite for ensuring sustainable high yields and climate benefits in RCG cultivations established on organic soils following drainage and peat extraction.     

Seasonal and spatial variations of methane emissions from coastal marshes in the northern Yellow River estuary, China

Aims and methods

To evaluate the seasonal and spatial variations of methane (CH₄) emissions and understand the controlling factors, we measured CH₄ fluxes and their environmental variables for the first time by a static chamber technique in high Suaeda salsa marsh (HSM), middle S. salsa marsh (MSM), low S. salsa marsh (LSM) and bare flat (BF) in the northern Yellow River estuary throughout a year.

Results

CH₄ emissions from coastal marsh varied throughout different times of the day and significant differences were observed in some sampling periods (p?<?0.05). Over all sampling periods, CH₄ fluxes averaged between ?0.392 mgCH₄ m^?2?h^?1 and 0.495 mgCH₄ m^?2?h^?1, and emissions occurred during spring (0.008 mgCH₄ m^?2?h^?1) and autumn (0.068 mgCH₄ m^?2?h^?1) while sinks were observed during summer (?0.110 mgCH₄ m^?2?h^?1) and winter (?0.009 mgCH₄ m^?2?h^?1). CH₄ fluxes from the four marshes were not significantly different (p?>?0.05), and emissions occurred in LSM (0.026 mgCH₄ m^?2?h^?1) and BF (0.055 mgCH₄ m^?2?h^?1) while sinks were observed in HSM (?0.035 mgCH₄ m^?2?h^?1) and MSM (?0.022 mgCH₄ m^?2?h^?1). The annual average CH₄ flux from the intertidal zone was 0.002 mgCH₄ m^?2?h^?1, indicating that coastal marsh acted as a weak CH₄ source. Temporal variations of CH₄ emission were related to the interactions of abiotic factors (temperatures, soil moisture and salinity) and the variations of limited C and mineral N in sediments, while spatial variations were mainly affected by the vegetation composition at spatial scale.

Conclusions

This study observed a large spatial variation of CH₄ fluxes across the coastal marsh of the Yellow River estuary (CV?=?7856.25 %), suggesting that the need to increase the spatial replicates at fine scales before the regional CH₄ budget was evaluated precisely. With increasing exogenous nitrogen loading to the Yellow River estuary, the magnitude of CH₄ emission might be enhanced, which should also be paid more attentions as the annual CH₄ inventory was assessed accurately.     

Impact of winter roads on boreal peatland carbon exchange

Across Canada's boreal forest, linear disturbances, including cutlines such as seismic lines and roads, crisscross the landscape to facilitate resource exploration and extraction; many of these linear disturbances cross peatland ecosystems. Changes in tree canopy cover and the compression of the peat by heavy equipment alter local thermal, hydrological, and ecological conditions, likely changing carbon exchange on the disturbance, and possibly in the adjacent peatland. We measured bulk density, water table, soil temperature, plant cover, and CO₂ and CH₄ flux along triplicate transects crossing a winter road through a wooded fen near Peace River, Alberta, Canada. Sample plots were located 1, 5, and 10 m from the road on both sides with an additional three plots on the road. Productivity of the overstory trees, when present, was also determined. The winter road had higher bulk density, shallower water table, higher graminoid cover, and thawed earlier than the adjacent peatland. Tree productivity and CO₂ flux varied between the plots, and there was no clear pattern in relation to distance from the road. The plots on the winter road acted as a greater CO₂ sink and greater CH₄ source compared to the adjacent peatland with plots on the winter road emitting on average (standard error) 479 (138) compared to 41 (10) mg CH₄ m^?2 day^?1 in the adjacent peatland. Considering both gases, global warming potential increased from 70 to 250 g CO₂e m^?2 year^?1 in the undisturbed area to 2100 g CO₂e m^?2 year^?1 on the winter road. Although carbon fluxes on any given cutline through peatland will vary depending on level of compaction, line width and vegetation community shifts, the large number of linear disturbances in Canada's boreal forest and slow recovery on peatland ecosites suggest they could represent an important anthropogenic greenhouse gas source.     

Considerable methane uptake by alpine grasslands despite the cold climate: in situ measurements on the central Tibetan Plateau, 2008–2013

The uptake of CH₄ by aerate soil plays a secondary role in the removal of tropospheric CH₄, but it is still highly uncertain in terms of its magnitude, spatial, and temporal variation. In an attempt to quantify the sink of the vast alpine grasslands (1 400 000 km²) of the Tibetan Plateau, we conducted in situ measurements in an alpine steppe (4730 m) and alpine meadow (4900 m) using the static chamber and gas chromatograph method. For the alpine steppe, measurements (2008–2013) suggested that there is large interannual variability in CH₄ uptake, ranging from ?48.8 to ?95.8 μg CH₄ m^?2 h^?1 (averaged of ?71.5 ± 2.5 μg CH₄ m^?2 h^?1), due to the variability in precipitation seasonality. The seasonal pattern of CH₄ uptakes in the form of stronger uptake in the early growing season and weaker uptake in the rainy season closely matched the precipitation seasonality and subsequent soil moisture variation. The relationships between alpine steppe CH₄ uptake and soil moisture/temperature are best depicted by a quadratic function and an exponential function (Q₁₀ = 1.67) respectively. Our measurements also showed that the alpine meadow soil (average of ?59.2 ± 3.7 μg CH₄ m^?2 h^?1) uptake less CH₄ than the alpine steppe and produces a similar seasonal pattern, which is negatively regulated by soil moisture. Our measurements quantified – at values far higher than those estimated by process‐based models – that both the alpine steppe and alpine meadow are considerable CH₄ sinks, despite the cold weather of this high‐altitude area. The consecutive measurements gathered in this study also highlight that precipitation seasonality tends to drive the interannual variation in CH₄ uptake, indicating that future study should be done to better characterize how CH₄ cycling might feedback to the more extreme climate.