Spatial Variation of Soil CO<Subscript>2</Subscript>, CH<Subscript>4</Subscript> and N<Subscript>2</Subscript>O Fluxes Across Topographical Positions in Tropical Forests of the Guiana Shield

The spatial variation of soil greenhouse gas fluxes (GHG; carbon dioxide—CO₂, methane—CH₄ and nitrous oxide—N₂O) remains poorly understood in highly complex ecosystems such as tropical forests. We used 240 individual flux measurements of these three GHGs from different soil types, at three topographical positions and in two extreme hydric conditions in the tropical forests of the Guiana Shield (French Guiana, South America) to (1) test the effect of topographical positions on GHG fluxes and (2) identify the soil characteristics driving flux variation in these nutrient-poor tropical soils. Surprisingly, none of the three GHG flux rates differed with topographical position. CO₂ effluxes covaried with soil pH, soil water content (SWC), available nitrogen and total phosphorus. The CH₄ fluxes were best explained by variation in SWC, with soils acting as a sink under drier conditions and as a source under wetter conditions. Unexpectedly, our study areas were generally sinks for N₂O and N₂O fluxes were partly explained by total phosphorus and available nitrogen concentrations. This first study describing the spatial variation of soil fluxes of the three main GHGs measured simultaneously in forests of the Guiana Shield lays the foundation for specific studies of the processes underlying the observed patterns.     

Impacts of climate and land use on N2O and CH4 fluxes from tropical ecosystems in the Mt. Kilimanjaro region,Tanzania

In this study, we quantify the impacts of climate and land use on soil N₂O and CH₄ fluxes from tropical forest, agroforest, arable and savanna ecosystems in Africa. To do so, we measured greenhouse gases (GHG) fluxes from 12 different ecosystems along climate and land‐use gradients at Mt. Kilimanjaro, combining long‐term in situ chamber and laboratory soil core incubation techniques. Both methods showed similar patterns of GHG exchange. Although there were distinct differences from ecosystem to ecosystem, soils generally functioned as net sources and sinks for N₂O and CH₄ respectively. N₂O emissions correlated positively with soil moisture and total soil nitrogen content. CH₄ uptake rates correlated negatively with soil moisture and clay content and positively with SOC. Due to moderate soil moisture contents and the dominance of nitrification in soil N turnover, N₂O emissions of tropical montane forests were generally low (<1.2 kg N ha^?1 year^?1), and it is likely that ecosystem N losses are driven instead by nitrate leaching (~10 kg N ha^?1 year^?1). Forest soils with well‐aerated litter layers were a significant sink for atmospheric CH₄ (up to 4 kg C ha^?1 year^?1) regardless of low mean annual temperatures at higher elevations. Land‐use intensification significantly increased the soil N₂O source strength and significantly decreased the soil CH₄ sink. Compared to decreases in aboveground and belowground carbon stocks enhanced soil non‐CO₂ GHG emissions following land‐use conversion from tropical forests to homegardens and coffee plantations were only a small factor in the total GHG budget. However, due to lower ecosystem carbon stock changes, enhanced N₂O emissions significantly contributed to total GHG emissions following conversion of savanna into grassland and particularly maize. Overall, we found that the protection and sustainable management of aboveground and belowground carbon and nitrogen stocks of agroforestry and arable systems is most crucial for mitigating GHG emissions from land‐use change.     

Soil-atmospheric exchange of CO2, CH4, and N2O in three subtropical forest ecosystems in southern China

The magnitude, temporal, and spatial patterns of soil‐atmospheric greenhouse gas (hereafter referred to as GHG) exchanges in forests near the Tropic of Cancer are still highly uncertain. To contribute towards an improvement of actual estimates, soil‐atmospheric CO₂, CH₄, and N₂O fluxes were measured in three successional subtropical forests at the Dinghushan Nature Reserve (hereafter referred to as DNR) in southern China. Soils in DNR forests behaved as N₂O sources and CH₄ sinks. Annual mean CO₂, N₂O, and CH₄ fluxes (mean±SD) were 7.7±4.6 Mg CO₂‐C ha^?1 yr^?1, 3.2±1.2 kg N₂O‐N ha^?1 yr^?1, and 3.4±0.9 kg CH₄‐C ha^?1 yr^?1, respectively. The climate was warm and wet from April through September 2003 (the hot‐humid season) and became cool and dry from October 2003 through March 2004 (the cool‐dry season). The seasonality of soil CO₂ emission coincided with the seasonal climate pattern, with high CO₂ emission rates in the hot‐humid season and low rates in the cool‐dry season. In contrast, seasonal patterns of CH₄ and N₂O fluxes were not clear, although higher CH₄ uptake rates were often observed in the cool‐dry season and higher N₂O emission rates were often observed in the hot‐humid season. GHG fluxes measured at these three sites showed a clear increasing trend with the progressive succession. If this trend is representative at the regional scale, CO₂ and N₂O emissions and CH₄ uptake in southern China may increase in the future in light of the projected change in forest age structure. Removal of surface litter reduced soil CO₂ effluxes by 17–44% in the three forests but had no significant effect on CH₄ absorption and N₂O emission rates. This suggests that microbial CH₄ uptake and N₂O production was mainly related to the mineral soil rather than in the surface litter layer.     

Impact of Grazing Intensity and Seasons on Greenhouse Gas Emissions in Tropical Grassland

Greenhouse gases (GHG) can be affected by grazing intensity, soil, and climate variables. This study aimed at assessing GHG emissions from a tropical pasture of Brazil to evaluate (i) how the grazing intensity affects the magnitude of GHG emissions; (ii) how season influences GHG production and consumption; and (iii) what are the key driving variables associated with GHG emissions. We measured under field conditions, during two years in a palisade-grass pasture managed with 3 grazing intensities: heavy (15 cm height), moderate (25 cm height), and light (35 cm height) N₂O, CH₄ and CO₂ fluxes using static closed chambers and chromatographic quantification. The greater emissions occurred in the summer and the lower in the winter. N₂O, CH₄, and CO₂ fluxes varied according to the season and were correlated with pasture grazing intensity, temperature, precipitation, % WFPS (water-filled pores space), and soil inorganic N. The explanatory variables differ according to the gas and season. Grazing intensity had a negative linear effect on annual cumulative N₂O emissions and a positive linear effect on annual cumulative CO₂ emissions. Grazing intensity, season, and year affected N₂O, CH₄, and CO₂ emissions. Tropical grassland can be a large sink of N₂O and CH₄. GHG emissions were explained for different key driving variables according to the season.     

Contribution of litter layer to soil greenhouse gas emissions in a temperate beech forest

Background and aims

The litter layer is a major source of CO₂, and it also influences soil-atmosphere exchange of N₂O and CH₄. So far, it is not clear how much of soil greenhouse gas (GHG) emission derives from the litter layer itself or is litter-induced. The present study investigates how the litter layer controls soil GHG fluxes and microbial decomposer communities in a temperate beech forest.

Methods

We removed the litter layer in an Austrian beech forest and studied responses of soil CO₂, CH₄ and N₂O fluxes and the microbial community via phospholipid fatty acids (PLFA). Soil GHG fluxes were determined with static chambers on 22 occasions from July 2012 to February 2013, and soil samples collected at 8 sampling events.

Results

Litter removal reduced CO₂ emissions by 30 % and increased temperature sensitivity (Q₁₀) of CO₂ fluxes. Diffusion of CH₄ into soil was facilitated by litter removal and CH₄ uptake increased by 16 %. This effect was strongest in autumn and winter when soil moisture was high. Soils without litter turned from net N₂O sources to slight N₂O sinks because N₂O emissions peaked after rain events in summer and autumn, which was not the case in litter-removal plots. Microbial composition was only transiently affected by litter removal but strongly influenced by seasonality.

Conclusions

Litter layers must be considered in calculating forest GHG budgets, and their influence on temperature sensitivity of soil GHG fluxes taken into account for future climate scenarios.

     

Effects of nitrogen deposition on the greenhouse gas fluxes from forest soils

Nitrogen (N) deposition can alter the rates of microbial N- and C- turnover, and thus can affect the fluxes of greenhouse gases (GHG, e.g., CO₂, CH₄, and N₂O) from forest soils. The effects of N deposition on the GHG fluxes from forest soils were reviewed in this paper. N deposition to forest soils have shown variable effects on the soil GHG fluxes from forest, including increases, decreases or unchanged rates depending on forest type, N status of the soil, and the rate and type of atmospheric N deposition. In forest ecosystems where biological processes are limited by N supply, N additions either stimulate soil respiration or have no significant effect, whereas in “N saturated” forest ecosystems, N additions decrease CO₂ emission, reduce CH₄ oxidation and elevate N₂O flux from the soil. The mechanisms and research methods about the effects of N deposition on GHG fluxes from forest soils were also reviewed in this paper. Finally, the present and future research needs about the effects of N deposition on the GHG fluxes from forest soils were discussed.     

Greenhouse gas fluxes of grazed and hayed wetland catchments in the U.S. Prairie Pothole Ecoregion

Wetland catchments are major ecosystems in the Prairie Pothole Region (PPR) and play an important role in greenhouse gases (GHG) flux. However, there is limited information regarding effects of land-use on GHG fluxes from these wetland systems. We examined the effects of grazing and haying, two common land-use practices in the region, on GHG fluxes from wetland catchments during 2007 and 2008. Fluxes of methane (CH₄), nitrous oxide (N₂O), and carbon dioxide (CO₂), along with soil water content and temperature, were measured along a topographic gradient every other week during the growing season near Ipswich, SD, USA. Closed, opaque chambers were used to measure fluxes of soil and plant respiration from native sod catchments that were grazed or left idle, and from recently restored catchments which were seeded with native plant species; half of these catchments were hayed once during the growing season. Catchments were adjacent to each other and had similar soils, soil nitrogen and organic carbon content, precipitation, and vegetation. When compared with idle catchments, grazing as a land-use had little effect on GHG fluxes. Likewise, haying had little effect on fluxes of CH₄ and N₂O compared with non-hayed catchments. Haying, however, did have a significant effect on combined soil and vegetative CO₂ flux in restored wetland catchments owing to the immediate and comprehensive effect haying has on plant productivity. This study also examined soil conditions that affect GHG fluxes and provides cumulative annual estimates of GHG fluxes from wetland catchment in the PPR.     

Canopy soil greenhouse gas dynamics in response to indirect fertilization across an elevation gradient of tropical montane forests

Canopy soils can significantly contribute to aboveground labile biomass, especially in tropical montane forests. Whether they also contribute to the exchange of greenhouse gases is unknown. To examine the importance of canopy soils to tropical forest‐soil greenhouse gas exchange, we quantified gas fluxes from canopy soil cores along an elevation gradient with 4 yr of nutrient addition to the forest floor. Canopy soil contributed 5–12 percent of combined (canopy + forest floor) soil CO₂ emissions but CH₄ and N₂O fluxes were low. At 2000 m, phosphorus decreased CO₂ emissions (>40%) and nitrogen slightly increased CH₄ uptake and N₂O emissions. Our results show that canopy soils may contribute significantly to combined soil greenhouse gas fluxes in montane regions with high accumulations of canopy soil. We also show that changes in fluxes could occur with chronic nutrient deposition.     

华南地区尾巨桉和马占相思人工林地表温室气体通量

为探索华南地区尾巨桉人工林和马占相思人工林地表温室气体的季节排放规律、排放通量和主控因子,采用静态箱-气相色谱法,对两种林型地表3种温室气体(CO_2、CH_4、N_2O)通量进行为期1年的逐月测定。结果表明:(1)尾巨桉人工林和马占相思人工林均为CO_2和N_2O的排放源,CH_4的吸收汇。马占相思林地表N_2O通量显著(P0.01)高于尾巨桉林,CO_2通量和CH_4通量无明显差异。(2)两种林型3种温室气体通量有着相似季节变化规律,地表CO_2通量均呈现雨季高旱季低的单峰规律;地表CH_4吸收通量表现为旱季高雨季低的单峰趋势;地表N_2O通量呈现雨季高旱季低且雨季内有两个峰值的排放规律。(3)地表CO_2、N_2O通量和土壤5 cm温度呈极显著(P0.01)正相关,3种温室气体地表通量同土壤含水量呈极显著(P0.01)或显著相关(P0.05)。(4)尾巨桉林和马占相思林温室气体年温室气体排放总量为31.014 t/hm~2和28.782 t/hm~2,均以CO_2排放占绝对优势(98.46%—99.15%),CH_4和N_2O处于次要地位。     

Inundation strongly stimulates nitrous oxide emissions from stems of the upland tree Fagus sylvatica and the riparian tree Alnus glutinosa

Background and aims

Nitrous oxide (N₂O) and methane (CH₄) can be emitted from surfaces of riparian plants. Data on the emission of these greenhouse gases by upland trees are scarce. We quantified CH₄ and N₂O emissions from stems of Fagus sylvatica, an upland tree, and Alnus glutinosa, a riparian tree.

Methods

The gas fluxes were investigated in mesocosms under non-flooded control conditions and during a flooding period using static chamber systems and gas chromatographic analyses.

Results

Despite differences in the presence of an aerenchyma system, both tree species emitted N₂O and CH₄ from the stems. Flooding caused a dramatic transient increase of N₂O stem emissions by factors of 740 (A. glutinosa) and even 14,230 (F. sylvatica). Stem emissions of CH₄ were low and even deposition was determined (F. sylvatica controls). The results suggest that CH₄ was transported mainly through the aerenchyma, whereas N₂O transport occurred in the xylem sap.

Conclusions

For the first time it has been demonstrated that upland trees such as F. sylvatica clearly significantly emit N₂O from their stems despite lacking an aerenchyma. If this result is confirmed in adult trees, upland forests may constitute a new and significant source of atmospheric N₂O.     

Enhanced CO2 uptake is marginally offset by altered fluxes of non-CO2 greenhouse gases in global forests and grasslands under N deposition

Despite the increasing impact of atmospheric nitrogen (N) deposition on terrestrial greenhouse gas (GHG) budget, through driving both the net atmospheric CO₂ exchange and the emission or uptake of non-CO₂ GHGs (CH₄ and N₂O), few studies have assessed the climatic impact of forests and grasslands under N deposition globally based on different bottom-up approaches. Here, we quantify the effects of N deposition on biomass C increment, soil organic C (SOC), CH₄ and N₂O fluxes and, ultimately, the net ecosystem GHG balance of forests and grasslands using a global comprehensive dataset. We showed that N addition significantly increased plant C uptake (net primary production) in forests and grasslands, to a larger extent for the aboveground C (aboveground net primary production), whereas it only caused a small or insignificant enhancement of SOC pool in both upland systems. Nitrogen addition had no significant effect on soil heterotrophic respiration (R_H) in both forests and grasslands, while a significant N-induced increase in soil CO₂ fluxes (R_S, soil respiration) was observed in grasslands. Nitrogen addition significantly stimulated soil N₂O fluxes in forests (76%), to a larger extent in grasslands (87%), but showed a consistent trend to decrease soil uptake of CH₄, suggesting a declined sink capacity of forests and grasslands for atmospheric CH₄ under N enrichment. Overall, the net GHG balance estimated by the net ecosystem production-based method (forest, 1.28 Pg CO₂-eq year⁻¹ vs. grassland, 0.58 Pg CO₂-eq year⁻¹) was greater than those estimated using the SOC-based method (forest, 0.32 Pg CO₂-eq year⁻¹ vs. grassland, 0.18 Pg CO₂-eq year⁻¹) caused by N addition. Our findings revealed that the enhanced soil C sequestration by N addition in global forests and grasslands could be only marginally offset (1.5%–4.8%) by the combined effects of its stimulation of N₂O emissions together with the reduced soil uptake of CH₄.     

Methane Concentration in the Heartwood of Living Trees and Estimated Methane Emission on Stems in Upland Forests

The stems of living trees in upland forests might contribute to the global methane (CH₄) source, but the contribution is poorly understood. We investigated CH₄ concentration in the heartwood of living trees in dominant upland forests using field campaign and subsequently evaluated the importance of stem CH₄ emission in the context of the global total. We found that only 0%, 9.8%, and 1.8% of stems of living trees had substantial CH₄ concentration in heartwood of?≥?10,000 μL L^–1 in the boreal, temperate, and tropical and subtropical upland forests investigated, respectively. CH₄ concentration in heartwood depended mainly upon tree species and subsequently soil moisture. Relationships fitted indicate that CH₄ concentration followed a power function with respect to water content in heartwood, whereas nitrous oxide (N₂O) or carbon dioxide (CO₂) concentration linearly increased with water content in heartwood. Stem CH₄ emission was estimated at approximately 0.2–2 Tg yr^–1 globally, corresponding to less than 0.4% of the global total including all natural plus anthropogenic sources. Water content in heartwood is positively associated with soil water content. Soil water content rarely exceeds 40% v/v in upland forests, indicating stem CH₄ emission occurs mainly in the areas of low-lying upland forests with occasionally moist soils. More attentions should be paid on low-lying upland forests and forested wetlands in future when stem CH₄ emission needs to be estimated in all forests.

Graphic abstract

     

Soil Greenhouse Gas Emissions in Response to Corn Stover Removal and Tillage Management Across the US Corn Belt

In-field measurements of direct soil greenhouse gas (GHG) emissions provide critical data for quantifying the net energy efficiency and economic feasibility of crop residue-based bioenergy production systems. A major challenge to such assessments has been the paucity of field studies addressing the effects of crop residue removal and associated best practices for soil management (i.e., conservation tillage) on soil emissions of carbon dioxide (CO₂), nitrous oxide (N₂O), and methane (CH₄). This regional survey summarizes soil GHG emissions from nine maize production systems evaluating different levels of corn stover removal under conventional or conservation tillage management across the US Corn Belt. Cumulative growing season soil emissions of CO₂, N₂O, and/or CH₄ were measured for 2–5 years (2008–2012) at these various sites using a standardized static vented chamber technique as part of the USDA-ARS’s Resilient Economic Agricultural Practices (REAP) regional partnership. Cumulative soil GHG emissions during the growing season varied widely across sites, by management, and by year. Overall, corn stover removal decreased soil total CO₂ and N₂O emissions by -4 and -7 %, respectively, relative to no removal. No management treatments affected soil CH₄ fluxes. When aggregated to total GHG emissions (Mg CO₂?eq ha^?1) across all sites and years, corn stover removal decreased growing season soil emissions by ?5?±?1 % (mean?±?se) and ranged from -36 % to 54 % (n?=?50). Lower GHG emissions in stover removal treatments were attributed to decreased C and N inputs into soils, as well as possible microclimatic differences associated with changes in soil cover. High levels of spatial and temporal variabilities in direct GHG emissions highlighted the importance of site-specific management and environmental conditions on the dynamics of GHG emissions from agricultural soils.     

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.     

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.     

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.     

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.     

Drainage increases CO2 and N2O emissions from tropical peat soils

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

Influence of experimental extreme water pulses on greenhouse gas emissions from soils

Climate models predict increased frequency and intensity of storm events, but it is unclear how extreme precipitation events influence the dynamics of soil fluxes for multiple greenhouse gases (GHGs). Intact soil mesocosms (0–10 cm depth) from a temperate forested watershed in the piedmont region of Maryland [two upland forest soils, and two hydric soils (i.e., wetland, creek bank)] were exposed to experimental water pulses with periods of drying, forcing soils towards extreme wet conditions under controlled temperature. Automated measurements (hourly resolution) of soil CO₂, CH₄, and N₂O fluxes were coupled with porewater chemistry analyses (i.e., pH, Eh, Fe, S, NO₃ ^?), and polymerase chain reaction–denaturing gradient gel electrophoresis to characterize changes in microbial community structure. Automated measurements quantified unexpected increases in emissions up to 245% for CO₂ (Wetland), >23,000% for CH₄ (Creek), and >110,000% for N₂O (Forest Soils) following pulse events. The Creek soil produced the highest soil CO₂ emissions, the Wetland soil produced the highest CH₄ emissions, and the Forest soils produced the highest N₂O emissions during the experiment. Using carbon dioxide equivalencies of the three GHGs, we determined the Creek soil contributed the most to a 20-year global warming potential (GWP; 30.3%). Forest soils contributed the most to the 100-year GWP (up to 53.7%) as a result of large N₂O emissions. These results provide insights on the influence of extreme wet conditions on porewater chemistry and factors controlling soil GHGs fluxes. Finally, this study addresses the need to test biogeochemical thresholds and responses of ecosystem functions to climate extremes.     

The Effect of Increased N Deposition on Nitrous oxide, Methane and Carbon dioxide Fluxes from Unmanaged Forest and Grassland Communities in Michigan

Atmospheric nitrogen deposition is anticipated to increase over the next decades with possible implications for future forest-atmosphere interactions. Increased soil N₂O emissions, depressed CH₄ uptake and depressed soil respiration CO₂ loss is considered a likely response to increased N deposition. This study examined fluxes of N₂O, CH₄ and CO₂ over two growing seasons from soils in unmanaged forest and grassland communities on abandoned agricultural areas in Michigan. All sites were subject to simulated increased N-deposition in the range of 1–3 g N m⁻² annually. Nitrous oxide fluxes and soil N concentrations in coniferous and grassland sites were on the whole unaffected by the increased N-inputs. It is noteworthy though that N₂O emissions increased three-fold in the coniferous sites in the first growing season in response to the low N treatment, although the response was barely significant (p<0.06). In deciduous forests, we observed increased levels of soil mineral N during the second year of N fertilization, however N₂O fluxes did not increase. Rates of methane oxidation were similar in all sites with no affect of field N application. Likewise, we did not observe any changes in soil CO₂ efflux in response to N additions. The combination of tillage history and vegetation type was important for the trace gas fluxes, i.e. soil CO₂ efflux was greater in successional grassland sites compared with the forested sites and CH₄ uptake was reduced in post-tillage coniferous- and successional sites compared with the old-growth deciduous site. Our results indicate that short-term increased N availability influenced individual processes linked to trace gas turnover in the soil independently from the ecosystem N status. However, changes in whole system fluxes were not evident and were very likely mediated by competitive N uptake processes.