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.     

Seasonal nitrous oxide and methane emissions across a subtropical estuarine salinity gradient

Currently, there is a lack of knowledge about GHG emissions, specifically N₂O and CH₄, in subtropical coastal freshwater wetland and mangroves in the southern hemisphere. In this study, we quantified the gas fluxes and substrate availability in a subtropical coastal wetland off the coast of southeast Queensland, Australia over a complete wet-dry seasonal cycle. Sites were selected along a salinity gradient ranging from marine (34 psu) in a mangrove forest to freshwater (0.05 psu) wetland, encompassing the range of tidal influence. Fluxes were quantified for CH₄ (range ?0.4–483 mg C–CH₄ h^?1 m^?2) and N₂O (?5.5–126.4 μg N–N₂O h^?1 m^?2), with the system acting as an overall source for CH₄ and N₂O (mean N₂O and CH₄ fluxes: 52.8 μg N–N₂O h^?1 m^?2 and 48.7 mg C–CH₄ h^?1 m^?2, respectively). Significantly higher N₂O fluxes were measured during the summer months (summer mean 64.2 ± 22.2 μg N–N₂O h^?1 m^?2; winter mean 33.1 ± 24.4 µg N–N₂O h^–1 m^?2) but not CH₄ fluxes (summer mean 30.2 ± 81.1 mg C–CH₄ h^?1 m^?2; winter mean 37.4 ± 79.6 mg C–CH₄ h^?1 m^?2). The changes with season are primarily driven by temperature and precipitation controls on the dissolved inorganic nitrogen (DIN) concentration. A significant spatial pattern was observed based on location within the study site, with highest fluxes observed in the freshwater tidal wetland and decreasing through the mangrove forest. The dissolved organic carbon (DOC) varied throughout the landscape and was correlated with higher CH₄ fluxes, but this was a nonlinear trend. DIN availability was dominated by N–NH₄ and correlated to changes in N₂O fluxes throughout the landscape. Overall, we did not observe linear relationships between CH₄ and N₂O fluxes and salinity, oxygen or substrate availability along the fresh-marine continuum, suggesting that this ecosystem is a mosaic of processes and responses to environmental changes.     

Spatial variability of N2O, CH4 and CO2 fluxes within the Xilin River catchment of Inner Mongolia, China: a soil core study

In order to identify the effects of land-use/cover types, soil types and soil properties on the soil-atmosphere exchange of greenhouse gases (GHG) in semiarid grasslands as well as provide a reliable estimate of the midsummer GHG budget, nitrous oxide (N₂O), methane (CH₄) and carbon dioxide (CO₂) fluxes of soil cores from 30 representative sites were determined in the upper Xilin River catchment in Inner Mongolia. The soil N₂O emissions across all of the investigated sites ranged from 0.18 to 21.8 μg N m^-2 h^-1, with a mean of 3.4 μg N m^-2 h^-1 and a coefficient of variation (CV, which is given as a percentage ratio of one standard deviation to the mean) as large as 130%. CH₄ fluxes ranged from -88.6 to 2,782.8 μg C m^-2 h^-1 (with a CV of 849%). Net CH₄ emissions were only observed from cores taken from a marshland site, whereas all of the other 29 investigated sites showed net CH₄ uptake (mean: -33.3 μg C m^-2 h^-1). CO₂ emissions from all sites ranged from 3.6 to 109.3 mg C m^-2 h^-1, with a mean value of 37.4 mg C m^-2 h^-1 and a CV of 66%. Soil moisture primarily and positively regulated the spatial variability in N₂O and CO₂ emissions (R²?=?0.15–0.28, P?<?0.05). The spatial variation of N₂O emissions was also influenced by soil inorganic N contents (P?<?0.05). By simply up-scaling the site measurements by the various land-use/cover types to the entire catchment area (3,900 km²), the fluxes of N₂O, CH₄ and CO₂ at the time of sampling (mid-summer 2007) were estimated at 29 t CO₂-C-eq d^-1, -26 t CO₂-C-eq d^-1 and 3,223 t C d^-1, respectively. This suggests that, in terms of assessing the spatial variability of total GHG fluxes from the soils at a semiarid catchment/region, intensive studies may focus on CO₂ exchange, which is dominating the global warming potential of midsummer soil-atmosphere GHG fluxes. In addition, average GHG fluxes in midsummer, weighted by the areal extent of these land-use/cover types in the region, were approximately -30.0 μg C m^-2 h^-1 for CH₄, 2.4 μg N m^-2 h^-1 for N₂O and 34.5 mg C m^-2 h^-1 for CO₂.     

Soil N and C trace gas fluxes and microbial soil N turnover in a sessile oak (Quercus petraea (Matt.) Liebl.) forest in Hungary

During two intensive field campaigns in summer and autumn 2004 nitrogen (N₂O, NO/NO₂) and carbon (CO₂, CH₄) trace gas exchange between soil and the atmosphere was measured in a sessile oak (Quercus petraea (Matt.) Liebl.) forest in Hungary. The climate can be described as continental temperate. Fluxes were measured with a fully automatic measuring system allowing for high temporal resolution. Mean N₂O emission rates were 1.5 μg N m⁻² h⁻¹ in summer and 3.4 μg N m⁻² h⁻¹ in autumn, respectively. Also mean NO emission rates were higher in autumn (8.4 μg N m⁻² h⁻¹) as compared to summer (6.0 μg N m⁻² h⁻¹). However, as NO₂ deposition rates continuously exceeded NO emission rates (−9.7 μg N m⁻² h⁻¹ in summer and −18.3 μg N m⁻² h⁻¹ in autumn), the forest soil always acted as a net NO _x sink. The mean value of CO₂ fluxes showed only little seasonal differences between summer (81.1 mg C m⁻² h⁻¹) and autumn (74.2 mg C m⁻² h⁻¹) measurements, likewise CH₄uptake (summer: −52.6 μg C m⁻² h⁻¹; autumn: −56.5 μg C m⁻² h⁻¹). In addition, the microbial soil processes net/gross N mineralization, net/gross nitrification and heterotrophic soil respiration as well as inorganic soil nitrogen concentrations and N₂O/CH₄ soil air concentrations in different soil depths were determined. The respiratory quotient (ΔCO_{2 resp} ΔO_{2 resp}⁻¹) for the uppermost mineral soil, which is needed for the calculation of gross nitrification via the Barometric Process Separation (BaPS) technique, was 0.8978 ± 0.008. The mean value of gross nitrification rates showed only little seasonal differences between summer (0.99 μg N kg⁻¹ SDW d⁻¹) and autumn measurements (0.89 μg N kg⁻¹ SDW d⁻¹). Gross rates of N mineralization were highest in the organic layer (20.1–137.9 μg N kg⁻¹ SDW d⁻¹) and significantly lower in the uppermost mineral layer (1.3–2.9 μg N kg⁻¹ SDW d⁻¹). Only for the organic layer seasonality in gross N mineralization rates could be demonstrated, with highest mean values in autumn, most likely caused by fresh litter decomposition. Gross mineralization rates of the organic layer were positively correlated with N₂O emissions and negatively correlated with CH₄ uptake, whereas soil CO₂ emissions were positively correlated with heterotrophic respiration in the uppermost mineral soil layer. The most important abiotic factor influencing C and N trace gas fluxes was soil moisture, while the influence of soil temperature on trace gas exchange rates was high only in autumn.     

Soil-atmosphere exchange of greenhouse gases in subtropical plantations of indigenous tree species

Indigenous broadleaf plantations are increasingly developing as a prospective silvicultural management approach for substituting in place of large pure conifer plantations in subtropical China. However, little information is known about the effects of tree species conversion on soil-atmosphere greenhouse gas (GHG) exchanges. Four adjacent monospecific plantations were selected in subtropical China to examine the effects of tree species on soil-atmosphere exchanges of N₂O, CH₄ and CO₂. One coniferous plantation was composed of Pinus massoniana (PM), and the three broadleaf plantations were Castanopsis hystrix (CH), Michelia macclurei (MM) and Mytilaria laosensis (ML). We found that mean soil N₂O and CO₂ emissions in the PM plantation were 4.34 μg N m^?2?h^?1 and 43.25 mg C m^?2?h^?1, respectively, lower than those in the broadleaf plantations (>5.25 μg N m^?2?h^?1 and >56.38 mg C m^?2?h^?1). The PM plantation soil had higher mean CH₄ uptake (39.03 μg C m^?2?h^?1) than the broadleaf plantation soils (<32.67 μg C m^?2?h^?1). Variations in soil N₂O emissions among tree species could be primarily explained by the differences in litter C:N ratio and soil total N stock. Differences in soil CH₄ uptake among tree species could be mostly attributed to the differences in mean soil CO₂ flux and water filled pore space (WFPS). Litter C:N ratio could largely account for variations in soil CO₂ emissions among tree species. This study confirms that there is no GHG benefit of converting PM plantation to broadleaf plantations in subtropical China. Therefore, the future strategy of tree species selection for substituting in place of large coniferous plantations in subtropical China needs to consider the potential effects of tree species on soil-atmosphere GHG exchanges.     

Physical and biological controls on trace gas fluxes in semi-arid urban ephemeral waterways

Rapid increases in human population and land transformation in arid and semi-arid regions are altering water, carbon (C) and nitrogen (N) cycles, yet little is known about how urban ephemeral stream channels in these regions affect biogeochemistry and trace gas fluxes. To address these knowledge gaps, we measured carbon dioxide (CO₂), nitrous oxide (N₂O), and methane (CH₄) before and after soil wetting in 16 ephemeral stream channels that vary in soil texture and organic matter in Tucson, AZ. Fluxes of CO₂ and N₂O immediately following wetting were among the highest ever published (up to 1,588 mg C m^?2 h^?1 and 3,121 μg N m^?2 h^?1). Mean post-wetting CO₂ and N₂O fluxes were significantly higher in the loam and sandy loam channels (286 and 194 mg C m^?2 h^?1; 168 and 187 μg N m^?2 h^?1) than in the sand channels (45 mg C m^?2 h^?1 and 7 μg N m^?2 h^?1). Factor analyses show that the effect of soil moisture, soil C and soil N on trace gas fluxes varied with soil texture. In the coarser sandy sites, trace gas fluxes were primarily controlled by soil moisture via physical displacement of soil gases and by organic soil C and N limitations on biotic processes. In the finer sandy loam sites trace gas fluxes and N-processing were primarily limited by soil moisture, soil organic C and soil N resources. In the loam sites, finer soil texture and higher soil organic C and N enhance soil moisture retention allowing for more biologically favorable antecedent conditions. Variable redox states appeared to develop in the finer textured soils resulting in wide ranging trace gas flux rates following wetting. These findings indicate that urban ephemeral channels are biogeochemical hotspots that can have a profound impact on urban C and N biogeochemical cycling pathways and subsequently alter the quality of localized water resources.     

Trace gas flux and the influence of short-term soil water and temperature dynamics in Australian sheep grazed pastures of differing productivity

Temperate pastures are often managed with P fertilizers and N₂-fixing legumes to maintain and increase pasture productivity which may lead to greater nitrous oxide (N₂O) emissions and reduced methane (CH₄) uptake. However, the diel and inter-daily variation in N₂O and CH₄ flux in pastures is poorly understood, especially in relation to key environmental drivers. We investigated the effect of pasture productivity, rainfall, and changing soil moisture and temperature upon short-term soil N₂O and CH₄ flux dynamics during spring in sheep grazed pasture systems in southeastern Australia. N₂O and CH₄ flux was measured continuously in a High P (23 kg P ha^?1 yr^?1) and No P pasture treatment and in a sheep camp area in a Low P (4 kg P ha^?1 yr^?1) pasture for a four week period in spring 2005 using an automated trace gas system. Although pasture productivity was three-fold greater in the High P than No P treatment, mean CH₄ uptake was similar (?6.3?±?SE 0.3 to ?8.6?±?0.4 μg C m^?2 hr^?1) as were mean N₂O emissions (6.5 to 7.9?±?0.8 μg N m^?2 hr^?1), although N₂O flux in the No P pasture did not respond to changing soil water conditions. N₂O emissions were greatest in the Low P sheep camp (12.4 μg?±?1.1 N m^?2 hr^?1) where there were also net CH₄ emissions of 5.2?±?0.5 μg C m^?2 hr^?1. There were significant, but weak, relationships between soil water and N₂O emissions, but not between soil water and CH₄ flux. The diel temperature cycle strongly influenced CH₄ and N₂O emissions, but this was often masked by the confounding covariate effects of changing soil water content. There were no consistently significant differences in soil mineral N or gross N transformation rates, however, measurements of substrate induced respiration (SIR) indicated that soil microbial processes in the highly productive pasture are more N limited than P limited after >20 years of P fertilizer addition. Increased productivity, through P fertilizer and legume management, did not significantly increase N₂O emissions, or reduce CH₄ uptake, during this 4 week measurement period, but the lack of an N₂O response to rainfall in the No P pasture suggests this may be evident over a longer measurement period. This study also suggests that small compacted and nutrient enriched areas of grazed pastures may contribute greatly to the overall N₂O and CH₄ trace gas balance.     

Nitrous oxide and methane fluxes from soils of the Orinoco savanna under different land uses

The study investigates the effect of land‐use change on nitrous oxide (N₂O) and methane (CH₄) fluxes from soil, in savanna ecosystems of the Orinoco region (Venezuela). Gas fluxes were measured by closed static chambers, in the wet and dry season, in representative systems of land management of the region: a cultivated pasture, an herbaceous savanna, a tree savanna and a woodland (control site). Higher N₂O emissions were observed in the cultivated pasture and in the herbaceous savanna compared with the tree savanna and the woodland, and differences were mainly related to fine soil particle content and soil volumetric water content measured in the studied sites. Overall N₂O emissions were quite low in all sites (0–1.58 mg N₂O‐N m^?2 day^?1). The cultivated pasture and the woodland savanna were on average weak CH₄ sinks (?0.05±0.07 and ?0.08±0.05 mg CH₄ m^?2 day^?1, respectively), whereas the herbaceous savanna and the tree savanna showed net CH₄ production (0.23±0.05 and 0.19±0.05 mg CH₄ m^?2 day^?1, respectively). Variations of CH₄ fluxes were mainly driven by variation of soil water‐filled pore space (WFPS), and a shift from net CH₄ consumption to net CH₄ production was observed at around 30% WFPS. Overall, the data suggest that conversion of woodland savanna to managed landscape could alter both CH₄ and N₂O fluxes; however, the magnitude of such variation depends on the soil characteristics and on the type of land management before conversion.     

Effect of water table on greenhouse gas emissions from peatland mesocosms

Peatland landscapes typically exhibit large variations in greenhouse gas (GHG) emissions due to microtopographic and vegetation heterogeneity. As many peatland budgets are extrapolated from small-scale chamber measurements it is important to both quantify and understand the processes underlying this spatial variability. Here we carried out a mesocosm study which allowed a comparison to be made between different microtopographic features and vegetation communities, in response to conditions of both static and changing water table. Three mesocosm types (hummocks?+?Juncus effusus, hummocks?+?Eriophorum vaginatum, and hollows dominated by moss) were subjected to two water table treatments (0–5 cm and 30–35 cm depth). Measurements were made of soil-atmosphere GHG exchange, GHG concentration within the peat profile and soil water solute concentrations. After 14 weeks the high water table group was drained and the low water table group flooded. Measurement intensity was then increased to examine the immediate response to change in water table position. Mean CO₂, CH₄ and N₂O exchange across all chambers was 39.8 μg m^?2 s^?1, 54.7 μg m^?2 h^?1 and ?2.9 μg m^?2 h^?1, respectively. Hence the GHG budget was dominated in this case by CO₂ exchange. CO₂ and N₂O emissions were highest in the low water table treatment group; CH₄ emissions were highest in the saturated mesocosms. We observed a strong interaction between mesocosm type and water table for CH₄ emissions. In contrast to many previous studies, we found that the presence of aerenchyma-containing vegetation reduced CH₄ emissions. A significant pulse in both CH₄ and N₂O emissions occurred within 1–2 days of switching the water table treatments. This pulsing could potentially lead to significant underestimation of landscape annual GHG budgets when widely spaced chamber measurements are upscaled.     

Quantification of N2O fluxes from soil–plant systems may be biased by the applied gas chromatograph methodology

With regard to measuring nitrous oxide (N₂O) emissions from biological sources, there are three most widely adopted methods that use gas chromatograph with an electron capture detector (GC–ECD). They use: (a) nitrogen (N₂) as the carrier gas (DN); (b) ascarite as a carbon dioxide (CO₂) trap with DN (DN-Ascarite); and (c) a mixture gas of argon and methane as the carrier (AM). Additional methods that use either a mixture of argon and methane (or of CO₂ and N₂) as a make-up gas with the carrier nitrogen or soda lime (or ascarite) as a CO₂ trap with the carrier helium have also been adopted in a few studies. To test the hypothesis that the use of DN sometimes considerably biases measurements of N₂O emissions from plants, soils or soil–plant systems, experiments were conducted involving DN, AM and DN-Ascarite. When using DN, a significant relationship appeared between CO₂ concentrations and the apparent N₂O concentrations in air samples. The use of DN led to significantly overestimated N₂O emissions from detached fresh plants in static chamber enclosures. Meanwhile, comparably lower emissions were found when using either the DN-Ascarite or AM methods. When an N₂O flux (from a soil or a soil–plant system), measured by DN in combination with sampling from the enclosure of a static opaque chamber, was greater than 200 μg N m^?2 h^?1, no significant difference was found between DN and DN-Ascarite. When the DN-measured fluxes were within the ranges of <?30, ?30–0, 0–30, 30–100 and 100–200 μg N m^?2 h^?1, significant differences that amounted to ?72, ?22, 5, 38 and 64 μg N m^?2 h^?1, respectively, appeared in comparison to DN-Ascarite. As a result, the DN measurements in rice–wheat and vegetable fields overestimated both annual total N₂O emissions (by 7–62%, p?<?0.05) and direct emission factors for applied nitrogen (by 6–65%). These results suggest the necessity of reassessing the available data determined from DN measurements before they are applied to inventory estimation. Further studies are required to explore appropriate approaches for the necessary reassessment. Our results also imply that the DN method should not be adopted for measuring N₂O emissions from weak sources (e.g., with intensities less than 200 μg N m^?2 h^?1). In addition, we especially do not recommend the use of DN to simultaneously measure N₂O and CO₂ with the same ECD.     

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.     

Nitrous oxide and methane exchange in two small temperate forest catchments—effects of hydrological gradients and implications for global warming potentials of forest soils

The magnitude of greenhouse gas (GHG) flux rates may be important in wet and intermediate wet forest soils, but published estimates are scarce. We studied the surface exchange of methane (CH₄) and nitrous oxide (N₂O) from soil along toposequences in two temperate deciduous forest catchments: Strødam and Vestskoven. The soil water regime ranged from fully saturated to aerated within the catchments. At Strødam the largest mean flux rates of N₂O (15 μg N₂O-N m^?2 h^?1) were measured at volumetric soil water contents (SWC) between 40 and 60% and associated with low soil pH compared to smaller mean flux rates of 0-5 μg N₂O-N m^?2 h^?1 for drier (SWC < 40%) and wet conditions (SWC > 80%). At Vestskoven the same response of N₂O to soil water content was observed. Average CH₄ flux rates were highly variable along the toposequences (?17 to 536 μg CH₄-C m^?2 h^?1) but emissions were only observed above soil water content of 45%. Scaled flux rates of both GHGs to catchment level resulted in emission of 322 and 211 kg CO₂-equivalents ha^?1 year^?1 for Strødam and Vestskoven, respectively, with N₂O contributing the most at both sites. Although the wet and intermediate wet forest soils occupied less than half the catchment area at both sites, the global warming potential (GWP) derived from N₂O and CH₄ was more than doubled when accounting for these wet areas in the catchments. The results stress the importance of wet soils in assessments of forest soil global warming potentials, as even small proportions of wet soils contributes substantially to the emissions of N₂O and CH₄.     

Nitrous oxide emissions from two alpine meadows in the Qinghai–Tibetan Plateau

Nitrous oxide (N₂O) emission was measured in a Kobresia humilis meadow and a Potentilla fruticosa meadow in the Qinghai–Tibet Plateau from June 2003 to July 2006. Five treatments were setup in the two alpine meadows. Two bare soil treatments were setup in the K. humilis meadow (BSK) and in the P. fruticosa meadow (BSP) by removing the above- and belowground plant biomass. Three plant community treatments were setup with one in the K. humilis meadow (herbaceous community in the K. humilis meadow-HCK) and two in the P. fruticosa meadow (herbaceous community in the P. fruticosa meadow-HCP, and shrub community in the P. fruticosa meadow-SCP). Nitrous oxide emission from BSP was estimated to be 38.1?±?3.6 μg m^?2 h^?1, significantly higher than from BSK (30.2?±?2.8 μg m^?2 h^?1) during the whole experiment period. Rates from the two herbaceous blocks (HCK and HCP) were close to 39.5 μg m^?2 h^?1 during the whole experimental period whereas shrub community (SCP) showed significant high emission rates of N₂O. Annual rate of N₂O emission was estimated to be 356.7?±?8.3 and 295.0?±?11.6 mg m^?2 year^?1 from the alpine P. fruticosa meadow and from the alpine K. humilis meadow, respectively. These results suggest that alpine meadows in the Qinghai–Tibetan Plateau are an important source of N₂O, contributing an average of 0.3 Tg N₂O year^?1. We concluded that N₂O emission will decrease, due to a predicted vegetation shift from shrubs to grasses imposed by overgrazing.     

Diffusive greenhouse gases fluxes from the surface of the Three Gorges Reservoir: Study at a site in Fuling

To investigate the water-air diffusive greenhouse gases (GHGs) fluxes from the Three Gorges Reservoir (TGR), a field experiment on carbon dioxide (CO₂), methane (CH₄) and nitrous oxide (N₂O) fluxes from water surface was carried out from March 2011 to August 2012 by floating static chamber method. The results showed that CO₂ was released to the atmosphere all the time and was less in autumn than in other seasons (P < 0.05). CH₄ was also released to the atmosphere throughout the year but more in summer than other three seasons (P < 0.05). N₂O flux was higher in autumn than other seasons (P < 0.05), and N₂O was absorbed from the atmosphere mainly in summer. Moreover, correlation analysis illustrated that CO₂ flux had significantly negative correlation with wind velocity (P < 0.05), whereas positive correlation with pH (P < 0.01) had been found. There was no significant correlation between CH₄ (or N₂O) flux and the measured environmental variables respectively (P > 0.05). Additionally, the annual fluxes of CO₂, CH₄ and N₂O were 140.45 ± 12.57 mg CO₂·m^?2 h^?1, 1.35 ± 0.14 mg CH₄·m^?2 h^?1 and 34.34 ± 11.64 μg N₂O·m^?2 h^?1, respectively. When compared to other reservoirs worldwide, the CO₂ and N₂O fluxes from TGR were higher than those from boreal and temperate reservoirs, but much lower than those from tropical reservoirs. CH₄ flux was lower than those from boreal, temperate and most tropical reservoirs. In our study, the surface area of the TGR emitted 1.42 × 10⁶ t CO₂, 1.19 × 10⁴ t CH₄ and 589.93 t N₂O in a year. The total GWP was 17.68 t CO₂-eq ha^?1 yr^?1, of which CO₂ flux was dominant (74.38%). Therefore, CO₂ was the main contributor of GHGs fluxes in our study and thus future researches should focus on how to reduce CO₂ fluxes from the surface of the TGR. TGR has a considerable contribution to regional GHG emissions.     

Emission of Methane and Nitrous Oxide by Australian Mangrove Ecosystems

Abstract: The fluxes of the greenhouse gases methane (CH₄) and nitrous oxide (N₂O) were measured in mangrove wetlands in Queensland, Australia, using the closed chamber technique. Large differences in the fluxes of both gases from different study sites were observed, which presumably depended on differences in substrate availability. CH₄ emission rates were in the range of 20 to 350 μg m^‐2 h^‐1, whereas N₂O fluxes were lower, amounting to ‐ 2 to 14 μg m^‐2 h^‐1. In general, the field sites with high substrate availability showed higher emissions than sites with poor nutrient supply. This assumption is supported by the observation of dramatically increased N₂O emissions (150 ‐ 400 μg m^‐2 h^‐1) if study sites were artificially fertilised with additional N. As expected, N fertilisation did not alter CH₄ fluxes during the period of investigation. In the present study, it was confirmed that the mangrove vegetation may play a role as a transport path for CH₄ and N₂O by facilitating diffusion out of the soil. Prop roots from Rhizophora stylosa emitted CH₄ and N₂O at rates of 2.6 and 3.3 μg m^‐2 root surface h^‐1, respectively, whereas the soil of this stand acted as a sink for CH₄. As a consequence, the ecosystem as a whole could constitute a CH₄ source despite CH₄ uptake by the soil. In contrast to prop roots, the presence of pneumatophores in Avicennia marina led to a significant increase in CH₄ emissions from mangrove soils, but did not enhance N₂O emissions. These findings indicate that mangrove ecosystems may be considered a significant source of N₂O and that anthropogenic nutrient input into these ecosystems will lead to enhanced source strengths. For an up‐scaling of greenhouse gas emissions from mangrove forests to a global scale, more information is needed, particularly on the significance of vegetation.     

Soil nitrous oxide and methane fluxes are low from a bioenergy crop (canola) grown in a semi-arid climate

Understanding nitrous oxide (N₂O) and methane (CH₄) fluxes from agricultural soils in semi‐arid climates is necessary to fully assess greenhouse gas emissions from bioenergy cropping systems, and to improve our knowledge of global terrestrial gaseous exchange. Canola is grown globally as a feedstock for biodiesel production, however, resulting soil greenhouse gas fluxes are rarely reported for semi‐arid climates. We measured soil N₂O and CH₄ fluxes from a rain‐fed canola crop in a semi‐arid region of south‐western Australia for 1 year on a subdaily basis. The site included N fertilized (75 kg N ha^?1 yr^?1) and nonfertilized plots. Daily N₂O fluxes were low (?1.5 to 4.7 g N₂O‐N ha^?1 day^?1) and culminated in an annual loss of 128 g N₂O‐N ha^?1 (standard error, 12 g N₂O‐N ha^?1) from N fertilized soil and 80 g N₂O‐N ha^?1 (standard error, 11 g N₂O‐N ha^?1) from nonfertilized soil. Daily CH₄ fluxes were also low (?10.3 to 11.9 g CH₄‐C ha^?1 day^?1), and did not differ with treatments, with an average annual net emission of 6.7 g CH₄–C ha^?1 (standard error, 20 g CH₄–C ha^?1). Greatest daily N₂O fluxes occurred when the soil was fallow, and following a series of summer rainfall events. Summer rainfall increased soil water contents and available N, and occurred when soil temperatures were >25 °C, and when there was no active plant growth to compete with soil microorganisms for mineralized N; conditions known to promote N₂O production. The proportion of N fertilizer emitted as N₂O, after correction for emissions from the no N fertilizer treatment, was 0.06%; 17 times lower than IPCC default value for the application of synthetic N fertilizers to land (1.0%). Soil greenhouse gas fluxes from bioenergy crop production in semi‐arid regions are likely to have less influence on the net global warming potential of biofuel production than in temperate climates.     

Microbial and Environmental Controls of Methane Fluxes Along a Soil Moisture Gradient in a Pacific Coastal Temperate Rainforest

Most studies of greenhouse gas fluxes from forest soils in the coastal rainforest have considered carbon dioxide (CO₂), whereas methane (CH₄) has not received the same attention. Soil hydrology is a key driver of CH₄ dynamics in ecosystems, but the impact on the function and distribution of the underlying microbial communities involved in CH₄ cycling and the resultant net CH₄ exchange is not well understood at this scale. We studied the growing season variations of in situ CH₄ fluxes, microbial gene abundances of methanotrophs (CH₄ oxidizers) and methanogens (CH₄ producers), soil hydrology, and nutrient availability in three typical forest types across a soil moisture gradient. CH₄ displayed a spatial variability changing from a net uptake in the upland soils (3.9–46 µmol CH₄ m^?2 h^?1) to a net emission in the wetter soils (0–90 μmol CH₄ m^?2 h^?1). Seasonal variations of CH₄ fluxes were related to soil hydrology in both upland and wet soils. Thus, in the upland soils, uptake rates increased with the decreasing soil moisture, whereas CH₄ emission was inversely related to the water table depth in the wet soils. Spatial variability of CH₄ exchange was related to the abundance of genes involved in CH₄ oxidation and production, but there was no indication of a temporal link between microbial groups and CH₄ exchange. Our data show that the abundances of genes involved in CH₄ oxidation and production are strongly influenced by soil moisture and each other and grouped by the upland–wetland classification but not forest type.     

Interaction of benthic microalgae and macrofauna in the control of benthic metabolism, nutrient fluxes and denitrification in a shallow sub-tropical coastal embayment (western Moreton Bay, Australia)

Benthic biogeochemistry and macrofauna were investigated six times over 1 year in a shallow sub-tropical embayment. Benthic fluxes of oxygen (annual mean ?918 μmol O₂ m^?2 h^?1), ammonium (NH₄ ⁺), nitrate (NO₃ ^?), dissolved organic nitrogen, dinitrogen gas (N₂), and dissolved inorganic phosphorus were positively related to OM supply (N mineralisation) and inversely related to benthic light (N assimilation). Ammonium (NH₄ ⁺), NO₃ ^? and N₂ fluxes (annual means +14.6, +15.9 and 44.6 μmol N m^?2 h^?1) accounted for 14, 16 and 53 % of the annual benthic N remineralisation respectively. Denitrification was dominated by coupled nitrification–denitrification throughout the study. Potential assimilation of nitrogen by benthic microalgae (BMA) accounted for between 1 and 30 % of remineralised N, and was greatest during winter when bottom light was higher. Macrofauna biomass tended to be highest at intermediate benthic respiration rates (?1,000 μmol O₂ m^?2 h^?1), and appeared to become limited as respiration increased above this point. While bioturbation did not significantly affect net fluxes, macrofauna biomass was correlated with increased light rates of NH₄ ⁺ flux which may have masked reductions in NH₄ ⁺ flux associated with BMA assimilation during the light. Peaks in net N₂ fluxes at intermediate respiration rates are suggested to be associated with the stimulation of potential denitrification sites due to bioturbation by burrowing macrofauna. NO₃ ^? fluxes suggest that nitrification was not significantly limited within respiration range measured during this study, however comparisons with other parts of Moreton Bay suggest that limitation of coupled nitrification–denitrification may occur in sub-tropical systems at respiration rates exceeding ?1,500 μmol O₂ m^?2 h^?1.     

Fluxes of N2O and CH4 from soils of savannas and seasonally-dry ecosystems

Aim Savannas and seasonally‐dry ecosystems cover a significant part of the world's land surface. If undisturbed, these ecosystems might be expected to show a net uptake of methane (CH₄) and a limited emission of nitrous oxide (N₂O). Land management has the potential to change dramatically the characteristics and gas exchange of ecosystems. The present work investigates the contribution of warm climate seasonally‐dry ecosystems to the atmospheric concentration of nitrous oxide and methane, and analyses the impact of land‐use change on N₂O and CH₄ fluxes from the ecosystems in question. Location Flux data reviewed here were collected from the literature; they come from savannas and seasonally‐dry ecosystems in warm climatic regions, including South America, India, Australasia and Mediterranean areas. Methods Data on gas fluxes were collected from the literature. Two factors were considered as determinants of the variation in gas fluxes: land management and season. Land management was grouped into: (1) control, (2) ‘burned only’ and (3) managed ecosystems. The season was categorized as dry or wet. In order to avoid the possibility that the influence of soil properties on gas fluxes might confound any differences caused by land management, sites were grouped in homogeneous clusters on the basis of soil properties, using multivariate analyses. Inter‐ and intra‐cluster analysis of gas fluxes were performed, taking into account the effects of season, land management and main vegetation types. Results Soils were often acid and nutrient‐poor, with low water retention. N₂O emissions were generally very low (median flux 0.32 mg N₂O m^?2 day^?1), and no significant differences were observed between woodland savannas and managed savannas. The highest fluxes (up to 12.9 mg N₂O m^?2 day^?1) were those on relatively fertile soils with high air‐filled porosity and water retention. The effect of season on N₂O production was evident only when sites were separated in homogeneous groups on the basis of soil properties. CH₄ fluxes varied over a wide range (?22.9 to 3.15 mg CH₄ m^?2 day^?1, where the negative sign denotes removal of gas from the atmosphere), with an annual average daily flux of ?0.48 ± 0.96 (SD) mg CH₄ m^?2 day^?1 in undisturbed (control) sites. Land‐use change dramatically reduced this CH₄ sink. Managed sites were weak sinks of CH₄ in the dry season and became sources of CH₄ in the wet season. This was particularly evident for pastures. Burning alone did not reduce soil net CH₄ oxidation, but decreased N₂O production. Main conclusions Despite the low potential for N₂O production, both in natural and managed conditions, tropical seasonally‐dry ecosystems represent a significant source of N₂O (4.4 Tg N₂O year^?1) on a global scale, as a consequence of the large area they occupy. The same environments represent a potential CH₄ sink of 5.17 Tg CH₄ year^?1. However, assuming that c. 30% of the tropical land is converted to different uses, the sink would be reduced to 3.2 Tg CH₄ year^?1. The limited information on fluxes from Mediterranean ecosystems does not allow a meaningful scaling up.     

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.