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.     

Methane and nitrous oxide fluxes in annual and perennial land-use systems of the irrigated areas in the Aral Sea Basin

Land use and agricultural practices can result in important contributions to the global source strength of atmospheric nitrous oxide (N₂O) and methane (CH₄). However, knowledge of gas flux from irrigated agriculture is very limited. From April 2005 to October 2006, a study was conducted in the Aral Sea Basin, Uzbekistan, to quantify and compare emissions of N₂O and CH₄ in various annual and perennial land-use systems: irrigated cotton, winter wheat and rice crops, a poplar plantation and a natural Tugai (floodplain) forest. In the annual systems, average N₂O emissions ranged from 10 to 150 μg N₂O-N m⁻² h⁻¹ with highest N₂O emissions in the cotton fields, covering a similar range of previous studies from irrigated cropping systems. Emission factors (uncorrected for background emission), used to determine the fertilizer-induced N₂O emission as a percentage of N fertilizer applied, ranged from 0.2% to 2.6%. Seasonal variations in N₂O emissions were principally controlled by fertilization and irrigation management. Pulses of N₂O emissions occurred after concomitant N-fertilizer application and irrigation. The unfertilized poplar plantation showed high N₂O emissions over the entire study period (30 μg N₂O-N m⁻² h⁻¹), whereas only negligible fluxes of N₂O (<2 μg N₂O-N m⁻² h⁻¹) occurred in the Tugai. Significant CH₄ fluxes only were determined from the flooded rice field: Fluxes were low with mean flux rates of 32 mg CH₄ m⁻² day⁻¹ and a low seasonal total of 35.2 kg CH₄ ha⁻¹. The global warming potential (GWP) of the N₂O and CH₄ fluxes was highest under rice and cotton, with seasonal changes between 500 and 3000 kg CO₂ eq. ha⁻¹. The biennial cotton–wheat–rice crop rotation commonly practiced in the region would average a GWP of 2500 kg CO₂ eq. ha⁻¹ yr⁻¹. The analyses point out opportunities for reducing the GWP of these irrigated agricultural systems by (i) optimization of fertilization and irrigation practices and (ii) conversion of annual cropping systems into perennial forest plantations, especially on less profitable, marginal lands.     

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.     

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 stand age on greenhouse gas fluxes from a Sitka spruce [Picea sitchensis (Bong.) Carr.] chronosequence on a peaty gley soil

The influence of forest stand age in a Picea sitchensis plantation on (1) soil fluxes of three greenhouse gases (GHGs – CO₂, CH₄ and N₂O) and (2) overall net ecosystem global warming potential (GWP), was investigated in a 2‐year study. The objective was to isolate the effect of forest stand age on soil edaphic characteristics (temperature, water table and volumetric moisture) and the consequent influence of these characteristics on the GHG fluxes. Fluxes were measured in a chronosequence in Harwood, England, with sites comprising 30‐ and 20‐year‐old second rotation forest and a site clearfelled (CF) some 18 months before measurement. Adjoining unforested grassland (UN) acted as a control. Comparisons were made between flux data, soil temperature and moisture data and, at the 30‐year‐old and CF sites, eddy covariance data for net ecosystem carbon (C) exchange (NEE). The main findings were: firstly, integrated CO₂ efflux was the dominant influence on the GHG budget, contributing 93–94% of the total GHG flux across the chronosequence compared with 6–7% from CH₄ and N₂O combined. Secondly, there were clear links between the trends in edaphic factors as the forest matured, or after clearfelling, and the emission of GHGs. In the chronosequence sites, annual fluxes of CO₂ were lower at the 20‐year‐old (20y) site than at the 30‐year‐old (30y) and CF sites, with soil temperature the dominant control. CH₄ efflux was highest at the CF site, with peak flux 491±54.5 μg m⁻² h⁻¹ and maximum annual flux 18.0±1.1 kg CH₄ ha⁻¹ yr⁻¹. No consistent uptake of CH₄ was noted at any site. A linear relationship was found between log CH₄ flux and the closeness of the water table to the soil surface across all sites. N₂O efflux was highest in the 30y site, reaching 108±38.3 μg N₂O‐N m⁻² h⁻¹ (171 μg N₂O m⁻² h⁻¹) in midsummer and a maximum annual flux of 4.7±1.2 kg N₂O ha⁻¹ yr⁻¹ in 2001. Automatic chamber data showed a positive exponential relationship between N₂O flux and soil temperature at this site. The relationship between N₂O emission and soil volumetric moisture indicated an optimum moisture content for N₂O flux of 40–50% by volume. The relationship between C : N ratio data and integrated N₂O flux was consistent with a pattern previously noted across temperate and boreal forest soils.     

Soil-atmosphere exchange of nitrous oxide and methane in New Zealand terrestrial ecosystems and their mitigation options: a review

The two non-CO₂ greenhouse gases (GHGs) nitrous oxide (N₂O) and methane (CH₄) comprise 54.8% of total New Zealand emissions. Nitrous oxide is mainly generated from mineral N originating from animal dung and urine, applied fertiliser N, biologically fixed N₂, and mineralisation of soil organic N. Even though about 96% of the anthropogenic CH₄ emitted in New Zealand is from ruminant animals (methanogenesis), methane uptake by aerobic soils (methanotrophy) can significantly contribute to the removal of CH₄ from the atmpsphere, as the global estimates confirm. Both the net uptake of CH₄ by soils and N₂O emissions from soils are strongly influenced by changes in land use and land management. Quantitative information on the fluxes of these two non-CO₂ GHGs is required for a range of land-use and land-management ecosystems to determine their contribution to the national emissions inventory, and for assessing the potential of mitigation options. Here we report soil N₂O fluxes and CH₄ uptake for a range of land-use and land-management systems collated from published and unpublished New Zealand studies. Nitrous oxide emissions are highest in dairy-grazed pastures (10–12 kg N₂O–N ha^?1 year^{? 1}), intermediate in sheep-grazed pastures, (4–6 kg N₂O–N ha^?1 year^?1), and lowest in forest, shrubland and ungrazed pasture soils (1–2 kg N₂O–N ha^?1 year^?1). N deposited in the form of animal urine and dung, and N applied as fertiliser, are the principal sources of N₂O production. Generally, N₂O emissions from grazed pasture soils are high when the soil water-filled pore-space is above field capacity, and net CH₄ uptake is low or absent. Although nitrification inhibitors have shown some promise in reducing N₂O emissions from grazed pasture systems, their efficacy as an integral part of farm management has yet to be tested. Methane uptake was highest for a New Zealand Beech forest soil (10–11 kg CH₄ ha^?1 year^?1), intermediate in some pine forest soils (4–6 kg CH₄ ha^?1 year^?1), and lowest in most pasture (<1 kg CH₄ ha^?1 year^?1) and cropped soils (1.5 kg CH₄ ha^?1 year^?1). Afforestation /reforestation of pastures results in increases in soil CH₄ uptake, largely as a result of increases in soil aeration status and changes in the population and activities of methanotrophs. Soil CH₄ uptake is also seasonally dependent, being about two to three times higher in a dry summer and autumn than in a wet winter. There are no practical ways yet available to reduce CH₄ emissions from agricultural systems. The mitigation options to reduce gaseous emissions are discussed and future research needs identified.     

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-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.     

N2O, CH4 and CO2 emissions from seasonal tropical rainforests and a rubber plantation in Southwest China

The main focus of this study was to evaluate the effects of soil moisture and temperature on temporal variation of N₂O, CO₂ and CH₄ soil-atmosphere exchange at a primary seasonal tropical rainforest (PF) site in Southwest China and to compare these fluxes with fluxes from a secondary forest (SF) and a rubber plantation (RP) site. Agroforestry systems, such as rubber plantations, are increasingly replacing primary and secondary forest systems in tropical Southwest China and thus effect the N₂O emission in these regions on a landscape level. The mean N₂O emission at site PF was 6.0 ± 0.1 SE μg N m⁻² h⁻¹. Fluxes of N₂O increased from <5 μg N m⁻² h⁻¹ during dry season conditions to up to 24.5 μg N m⁻² h⁻¹ with re-wetting of the soil by the onset of first rainfall events. Comparable fluxes of N₂O were measured in the SF and RP sites, where mean N₂O emissions were 7.3 ± 0.7 SE μg N m⁻² h⁻¹ and 4.1 ± 0.5 SE μg N m⁻² h⁻¹, respectively. The dependency of N₂O fluxes on soil moisture levels was demonstrated in a watering experiment, however, artificial rainfall only influenced the timing of N₂O emission peaks, not the total amount of N₂O emitted. For all sites, significant positive correlations existed between N₂O emissions and both soil moisture and soil temperature. Mean CH₄ uptake rates were highest at the PF site (−29.5 ± 0.3 SE μg C m⁻² h⁻¹), slightly lower at the SF site (−25.6 ± 1.3 SE μg C m⁻² h⁻¹) and lowest for the RP site (−5.7 ± 0.5 SE μg C m⁻² h⁻¹). At all sites, CH₄ uptake rates were negatively correlated with soil moisture, which was also reflected in the lower uptake rates measured in the watering experiment. In contrast to N₂O emissions, CH₄ uptake did not significantly correlate with soil temperature at the SF and RP sites, and only weakly correlated at the PF site. Over the 2 month measurement period, CO₂ emissions at the PF site increased significantly from 50 mg C m⁻² h⁻¹ up to 100 mg C m⁻² h⁻¹ (mean value 68.8 ± 0.8 SE mg C m⁻² h⁻¹), whereas CO₂ emissions at the SF and RP site where quite stable and varied only slightly around mean values of 38.0 ± 1.8 SE mg C m⁻² h⁻¹ (SF) and 34.9 ± 1.1 SE mg C m⁻² h⁻¹ (RP). A dependency of soil CO₂ emissions on changes in soil water content could be demonstrated for all sites, thus, the watering experiment revealed significantly higher CO₂ emissions as compared to control chambers. Correlation of CO₂ emissions with soil temperature was significant at the PF site, but weak at the SF and not evident at the RP site. Even though we demonstrated that N and C trace gas fluxes significantly varied on subdaily and daily scales, weekly measurements would be sufficient if only the sink/ source strength of non-managed tropical forest sites needs to be identified.     

The Impact of Nitrogen Placement and Tillage on NO, N2O, CH4 and CO2 Fluxes from a Clay Loam Soil

To evaluate the impact of N placement depth and no-till (NT) practice on the emissions of NO, N₂O, CH₄ and CO₂ from soils, we conducted two N placement experiments in a long-term tillage experiment site in northeastern Colorado in 2004. Trace gas flux measurements were made 2–3 times per week, in zero-N fertilizer plots that were cropped continuously to corn (Zea mays L.) under conventional-till (CT) and NT. Three N placement depths, replicated four times (5, 10 and 15 cm in Exp. 1 and 0, 5 and 10 cm in Exp. 2, respectively) were used. Liquid urea–ammonium nitrate (UAN, 224 kg N ha⁻¹) was injected to the desired depth in the CT- or NT-soils in each experiment. Mean flux rates of NO, N₂O, CH₄ and CO₂ ranged from 3.9 to 5.2 μg N m⁻² h⁻¹, 60.5 to 92.4 μg N m⁻² h⁻¹, −0.8 to 0.5 μg C m⁻² h⁻¹, and 42.1 to 81.7 mg C m⁻² h⁻¹ in both experiments, respectively. Deep N placement (10 and 15 cm) resulted in lower NO and N₂O emissions compared with shallow N placement (0 and 5 cm) while CH₄ and CO₂ emissions were not affected by N placement in either experiment. Compared with N placement at 5 cm, for instance, averaged N₂O emissions from N placement at 10 cm were reduced by more than 50% in both experiments. Generally, NT decreased NO emission and CH₄ oxidation but increased N₂O emissions compared with CT irrespective of N placement depths. Total net global warming potential (GWP) for N₂O, CH₄ and CO₂ was reduced by deep N placement only in Exp. 1 but was increased by NT in both experiments. The study results suggest that deep N placement (e.g., 10 cm) will be an effective option for reducing N oxide emissions and GWP from both fertilized CT- and NT-soils.     

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.     

CH4 and N2O emissions from smallholder agricultural systems on tropical peatlands in Southeast Asia

There are limited data for greenhouse gas (GHG) emissions from smallholder agricultural systems in tropical peatlands, with data for non-CO₂ emissions from human-influenced tropical peatlands particularly scarce. The aim of this study was to quantify soil CH₄ and N₂O fluxes from smallholder agricultural systems on tropical peatlands in Southeast Asia and assess their environmental controls. The study was carried out in four regions in Malaysia and Indonesia. CH₄ and N₂O fluxes and environmental parameters were measured in cropland, oil palm plantation, tree plantation and forest. Annual CH₄ emissions (in kg CH₄ ha⁻¹ year⁻¹) were: 70.7 ± 29.5, 2.1 ± 1.2, 2.1 ± 0.6 and 6.2 ± 1.9 at the forest, tree plantation, oil palm and cropland land-use classes, respectively. Annual N₂O emissions (in kg N₂O ha⁻¹ year⁻¹) were: 6.5 ± 2.8, 3.2 ± 1.2, 21.9 ± 11.4 and 33.6 ± 7.3 in the same order as above, respectively. Annual CH₄ emissions were strongly determined by water table depth (WTD) and increased exponentially when annual WTD was above −25 cm. In contrast, annual N₂O emissions were strongly correlated with mean total dissolved nitrogen (TDN) in soil water, following a sigmoidal relationship, up to an apparent threshold of 10 mg N L⁻¹ beyond which TDN seemingly ceased to be limiting for N₂O production. The new emissions data for CH₄ and N₂O presented here should help to develop more robust country level ‘emission factors’ for the quantification of national GHG inventory reporting. The impact of TDN on N₂O emissions suggests that soil nutrient status strongly impacts emissions, and therefore, policies which reduce N-fertilisation inputs might contribute to emissions mitigation from agricultural peat landscapes. However, the most important policy intervention for reducing emissions is one that reduces the conversion of peat swamp forest to agriculture on peatlands in the first place.     

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.     

不同恢复方式下大兴安岭重度火烧迹地林地土壤温室气体通量

为研究大兴安岭重度火烧迹地在不同恢复方式下林地土壤CO₂、CH₄和N₂O排放特征及其影响因素,采用静态箱/气相色谱法,在2017年生长季（6月-9月）对3种恢复方式（人工更新、天然更新和人工促进天然更新）林地土壤温室气体CO₂、CH₄、N₂O通量进行了原位观测。研究结果表明：（1）3种恢复方式林地土壤在生长季均为大气CO₂、N₂O的源,CH₄的汇;生长季林地土壤CO₂排放通量大小关系为人工促进天然更新（（634.40±246.52）mg m^-2 h^-1） > 人工更新（（603.63±213.22）mg m^-2 h^-1） > 天然更新（（575.81±244.12）mg m^-2 h^-1）,3种恢复方式间无显著差异;人工更新林地土壤CH₄吸收通量显著高于人工促进天然更新;天然更新林地土壤N₂O排放通量显著高于其他两种恢复方式。（2）土壤温度是影响3种恢复方式林地土壤温室气体通量的关键因素;土壤水分仅对人工更新林地土壤N₂O通量有极显著影响（P < 0.01）;3种恢复方式林地土壤CO₂通量与大气湿度具有极显著的响应（P < 0.01）;土壤pH仅与天然更新林地土壤CO₂通量显著相关（P < 0.05）;土壤全氮含量仅与人工促进天然更新林地土壤CH₄通量显著相关（P < 0.05）。（3）基于100年尺度,由3种温室气体计算全球增温潜势得出,人工促进天然更新（1.83×10⁴ kg CO₂/hm²） > 人工更新（1.74×10⁴ kg CO₂/hm²） > 天然更新（1.67×10⁴ kg CO₂/hm²）。（4）阿木尔地区林地土壤年生长季CO₂和N₂O排放量为8.85×10⁶ t和1.88×10² t,CH₄吸收量为1.05×10³ t。     

Effect of biochar amendment on the soil-atmosphere exchange of greenhouse gases from an intensive subtropical pasture in northern New South Wales, Australia

We assessed the effect of biochar incorporation into the soil on the soil-atmosphere exchange of the greenhouse gases (GHG) from an intensive subtropical pasture. For this, we measured N₂O, CH₄ and CO₂ emissions with high temporal resolution from April to June 2009 in an existing factorial experiment where cattle feedlot biochar had been applied at 10 t ha^?1 in November 2006. Over the whole measurement period, significant emissions of N₂O and CO₂ were observed, whereas a net uptake of CH₄ was measured. N₂O emissions were found to be highly episodic with one major emission pulse (up to 502 ??g N₂O-N m^?2 h^?1) following heavy rainfall. There was no significant difference in the net flux of GHGs from the biochar amended vs. the control plots. Our results demonstrate that intensively managed subtropical pastures on ferrosols in northern New South Wales of Australia can be a significant source of GHG. Our hypothesis that the application of biochar would lead to a reduction in emissions of GHG from soils was not supported in this field assessment. Additional studies with longer observation periods are needed to clarify the long term effect of biochar amendment on soil microbial processes and the emission of GHGs under field conditions.     

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.     

Urbanization can accelerate climate change by increasing soil N2O emission while reducing CH4 uptake

Urban land-use change has the potential to affect local to global biogeochemical carbon (C) and nitrogen (N) cycles and associated greenhouse gas (GHG) fluxes. We conducted a meta-analysis to (1) assess the effects of urbanization-induced land-use conversion on soil nitrous oxide (N₂O) and methane (CH₄) fluxes, (2) quantify direct N₂O emission factors (EF_d) of fertilized urban soils used, for example, as lawns or forests, and (3) identify the key drivers leading to flux changes associated with urbanization. On average, urbanization increases soil N₂O emissions by 153%, to 3.0 kg N ha⁻¹ year⁻¹, while rates of soil CH₄ uptake are reduced by 50%, to 2.0 kg C ha⁻¹ year⁻¹. The global mean annual N₂O EF_d of fertilized lawns and urban forests is 1.4%, suggesting that urban soils can be regional hotspots of N₂O emissions. On a global basis, conversion of land to urban greenspaces has increased soil N₂O emission by 0.46 Tg N₂O-N year⁻¹ and decreased soil CH₄ uptake by 0.58 Tg CH₄-C year⁻¹. Urbanization driven changes in soil N₂O emission and CH₄ uptake are associated with changes in soil properties (bulk density, pH, total N content, and C/N ratio), increased temperature, and management practices, especially fertilizer use. Overall, our meta-analysis shows that urbanization increases soil N₂O emissions and reduces the role of soils as a sink for atmospheric CH₄. These effects can be mitigated by avoiding soil compaction, reducing fertilization of lawns, and by restoring native ecosystems in urban landscapes.     

Diurnal fluctuations of dissolved nitrous oxide (N2O) concentrations and estimates of N2O emissions from a spring-fed river: implications for IPCC methodology

There is uncertainty in the estimates of indirect nitrous oxide (N₂O) emissions as defined by the Intergovernmental Panel on Climate Change (IPCC). The uncertainty is due to the challenge and dearth of in situ measurements. Recent work in a subtropical stream system has shown the potential for diurnal variability to influence the downstream N transfer, N form, and estimates of in‐stream N₂O production. Studies in temperate stream systems have also shown diurnal changes in stream chemistry. The objectives of this study were to measure N₂O fluxes and dissolved N₂O concentrations from a spring‐fed temperate river to determine if diurnal cycles were occurring. The study was performed during a 72 h period, over a 180 m reach, using headspace chamber methodology. Significant diurnal cycles were observed in radiation, river temperature and chemistry including dissolved N₂O‐N concentrations. These data were used to further assess the IPCC methodology and experimental methodology used. River NO₃‐N and N₂O‐N concentrations averaged 3.0 mg L⁻¹ and 1.6 μg L⁻¹, respectively, with N₂O saturation reaching a maximum of 664%. The N₂O‐N fluxes, measured using chamber methodology, ranged from 52 to 140 μg m⁻² h⁻¹ while fluxes predicted using the dissolved N₂O concentration ranged from 13 to 25 μg m⁻² h⁻¹. The headspace chamber methodology may have enhanced the measured N₂O flux and this is discussed. Diurnal cycles in N₂O% saturation were not large enough to influence downstream N transfer or N form with variability in measured N₂O fluxes greater and more significant than diurnal variability in N₂O% saturation. The measured N₂O fluxes, extrapolated over the study reach area, represented only 6 × 10⁻⁴% of the NO₃‐N that passed through the study reach over a 72 h period. This is only 0.1% of the IPCC calculated flux.     

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.     

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.