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.     

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.     

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.     

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.     

Responses of CO2, N2O and CH4 fluxes between atmosphere and forest soil to changes in multiple environmental conditions

To investigate the effects of multiple environmental conditions on greenhouse gas (CO₂, N₂O, CH₄) fluxes, we transferred three soil monoliths from Masson pine forest (PF) or coniferous and broadleaved mixed forest (MF) at Jigongshan to corresponding forest type at Dinghushan. Greenhouse gas fluxes at the in situ (Jigongshan), transported and ambient (Dinghushan) soil monoliths were measured using static chambers. When the transported soil monoliths experienced the external environmental factors (temperature, precipitation and nitrogen deposition) at Dinghushan, its annual soil CO₂ emissions were 54% in PF and 60% in MF higher than those from the respective in situ treatment. Annual soil N₂O emissions were 45% in PF and 44% in MF higher than those from the respective in situ treatment. There were no significant differences in annual soil CO₂ or N₂O emissions between the transported and ambient treatments. However, annual CH₄ uptake by the transported soil monoliths in PF or MF was not significantly different from that at the respective in situ treatment, and was significantly lower than that at the respective ambient treatment. Therefore, external environmental factors were the major drivers of soil CO₂ and N₂O emissions, while soil was the dominant controller of soil CH₄ uptake. We further tested the results by developing simple empirical models using the observed fluxes of CO₂ and N₂O from the in situ treatment and found that the empirical models can explain about 90% for CO₂ and 40% for N₂O of the observed variations at the transported treatment. Results from this study suggest that the different responses of soil CO₂, N₂O, CH₄ fluxes to changes in multiple environmental conditions need to be considered in global change study.     

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.     

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.     

The greenhouse gas balance of European grasslands

The greenhouse gas (GHG) balance of European grasslands (EU‐28 plus Norway and Switzerland), including CO₂, CH₄ and N₂O, is estimated using the new process‐based biogeochemical model ORCHIDEE‐GM over the period 1961–2010. The model includes the following: (1) a mechanistic representation of the spatial distribution of management practice; (2) management intensity, going from intensively to extensively managed; (3) gridded simulation of the carbon balance at ecosystem and farm scale; and (4) gridded simulation of N₂O and CH₄ emissions by fertilized grassland soils and livestock. The external drivers of the model are changing animal numbers, nitrogen fertilization and deposition, land‐use change, and variable CO₂ and climate. The carbon balance of European grassland (NBP) is estimated to be a net sink of 15 ± 7 g C m^?2 year^?1 during 1961–2010, equivalent to a 50‐year continental cumulative soil carbon sequestration of 1.0 ± 0.4 Pg C. At the farm scale, which includes both ecosystem CO₂ fluxes and CO₂ emissions from the digestion of harvested forage, the net C balance is roughly halved, down to a small sink, or nearly neutral flux of 8 g C m^?2 year^?1. Adding CH₄ and N₂O emissions to net ecosystem exchange to define the ecosystem‐scale GHG balance, we found that grasslands remain a net GHG sink of 19 ± 10 g C‐CO₂ equiv. m^?2 year^?1, because the CO₂ sink offsets N₂O and grazing animal CH₄ emissions. However, when considering the farm scale, the GHG balance (NGB) becomes a net GHG source of ?50 g C‐CO₂ equiv. m^?2 year^?1. ORCHIDEE‐GM simulated an increase in European grassland NBP during the last five decades. This enhanced NBP reflects the combination of a positive trend of net primary production due to CO₂, climate and nitrogen fertilization and the diminishing requirement for grass forage due to the Europe‐wide reduction in livestock numbers.     

Woody biochar's greenhouse gas mitigation potential across fertilized and unfertilized agricultural soils and soil moisture regimes

Biochar has been widely researched as an important technology for climate smart agriculture, yet work is still necessary to identify the magnitude of potential greenhouse gas (GHG) mitigation and mechanisms involved. This study measured slow‐pyrolysis wood‐derived biochar's impact on GHG efflux, mineral N dynamics, and soil organic C in a series of two incubations across fertilized and unfertilized agricultural soils and soil moisture regimes. This research explored the magnitude of biochar's full GHG mitigation potential and drivers of such impacts. Results of this incubation indicate slow‐pyrolysis wood‐derived biochar has potential to provide annual emission reductions of 0.58–1.72 Mg CO₂‐eq ha^?1 at a 25 Mg ha^?1 biochar application rate. The greatest GHG mitigation potential was from C sequestration and nitrous oxide (N₂O) reduction in mineral N fertilized soils, with minimal impacts on N₂O emissions in unfertilized soils, carbon dioxide (CO₂) emissions, and methane (CH₄) uptake. Analysis of mineral N dynamics in the bulk soil and on biochar isolates indicated that neither biochar impacts on net mineralization and nitrification nor retention of ammonium () on biochar isolates could explain biochar's N₂O reduction. Instead, biochar amendments exhibited consistent N₂O emission reductions relative to the N₂O emission in the control soil regardless of soil type and fertilization. Results across a soil moisture gradient suggest that woody biochar may aerate soils shifting redox conditions and subsequent N₂O production. Understanding the magnitude of biochar's GHG reduction potential and the mechanisms driving these effects can help inform biochar modeling efforts, explain field results and identify agricultural applications that maximize biochar's full GHG mitigation potential.     

Understory vegetation management affected greenhouse gas emissions and labile organic carbon pools in an intensively managed Chinese chestnut plantation

Background and aims

The impact of understory vegetation control or replacement with selected plant species, which are common forest plantation management practices, on soil C pool and greenhouse gas (GHG, including CO₂, CH₄ and N₂O) emissions are poorly understood. The objective of this paper was to investigate the effects of understory vegetation management on the dynamics of soil GHG emissions and labile C pools in an intensively managed Chinese chestnut (Castanea mollissima Blume) plantation in subtropical China.

Methods

A 12-month field experiment was conducted to study the dynamics of soil labile C pools and GHG emissions in a Chinese chestnut plantation under four different understory management practices: control (Control), understory removal (UR), replacement of understory vegetation with Medicago sativa L. (MS), and replacement with Lolium perenne L. (LP). Soil GHG emissions were determined using the static chamber/GC technique.

Results

Understory management did not change the seasonal pattern of soil GHG emissions; however, as compared with the Control, the UR treatment increased soil CO₂ and N₂O emissions and CH₄ uptake, and the MS and LP treatments increased CO₂ and N₂O emissions and reduced CH₄ uptake (P?<?0.05 for all treatment effects, same below). The total global warming potential (GWP) of GHG emissions in the Control, UR, MS, and LP treatments were 36.56, 39.40, 42.36, and 42.99 Mg CO₂ equivalent (CO₂-e) ha^?1 year^?1, respectively, with CO₂ emission accounting for more than 95 % of total GWP regardless of the understory management treatment. The MS and LP treatments increased soil organic C (SOC), total N (TN), soil water soluble organic C (WSOC) and microbial biomass C (MBC), while the UR treatment decreased SOC, TN and NO₃ ^?-N but had no effect on WSOC and MBC. Soil GHG emissions were correlated with soil temperature and WSOC across the treatments, but had no relationship with soil moisture content and MBC.

Conclusions

Although replacing competitive understory vegetation with legume or less competitive non-legume species increased soil GHG emissions and total GWP, such treatments also increased soil C and N pools and are therefore beneficial for increasing soil C storage, maintaining soil fertility, and enhancing the productivity of Chinese chestnut plantations.     

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.     

CO2 uptake is offset by CH4 and N2O emissions in a poplar short‐rotation coppice

The need for renewable energy sources will lead to a considerable expansion in the planting of dedicated fast‐growing biomass crops across Europe. These are commonly cultivated as short‐rotation coppice (SRC), and currently poplar (Populus spp.) is the most widely planted. In this study, we report the greenhouse gas (GHG) fluxes of carbon dioxide (CO₂), methane (CH₄) and nitrous oxide (N₂O) measured using eddy covariance technique in an SRC plantation for bioenergy production. Measurements were made during the period 2010–2013, that is, during the first two rotations of the SRC. The overall GHG balance of the 4 years of the study was an emission of 1.90 (±1.37) Mg CO₂eq ha^?1; this indicated that soil trace gas emissions offset the CO₂ uptake by the plantation. CH₄ and N₂O contributed almost equally to offset the CO₂ uptake of ?5.28 (±0.67) Mg CO₂eq ha^?1 with an overall emission of 3.56 (±0.35) Mg CO₂eq ha^?1 of N₂O and of 3.53 (±0.85) Mg CO₂eq ha^?1 of CH₄. N₂O emissions mostly occurred during one single peak a few months after the site was converted to SRC; this peak comprised 44% of the total N₂O loss during the two rotations. Accurately capturing emission events proved to be critical for deriving correct estimates of the GHG balance. The nitrogen (N) content of the soil and the water table depth were the two drivers that best explained the variability in N₂O and CH_4, respectively. This study underlines the importance of the ‘non‐CO₂ GHGs’ on the overall balance. Further long‐term investigations of soil trace gas emissions should monitor the N content and the mineralization rate of the soil, as well as the microbial community, as drivers of the trace gas emissions.     

Cropland intensification mediates the radiative balance of greenhouse gas emissions and soil carbon sequestration in maize systems of sub-Saharan Africa

Sub-Saharan Africa (SSA) must undertake proper cropland intensification for higher crop yields while minimizing climate impacts. Unfortunately, no studies have simultaneously quantified greenhouse gas (GHG; CO₂, CH₄, and N₂O) emissions and soil organic carbon (SOC) change in SSA croplands, leaving it a blind spot in the accounting of global warming potential (GWP). Here, based on 2-year field monitoring of soil emissions of CO₂, CH₄, and N₂O, as well as SOC changes in two contrasting soil types (sandy vs. clayey), we provided the first, full accounting of GWP for maize systems in response to cropland intensifications (increasing nitrogen rates and in combination with crop residue return) in SSA. To corroborate our field observations on SOC change (i.e., 2-year, a short duration), we implemented a process-oriented model parameterized with field data to simulate SOC dynamic over time. We further tested the generality of our findings by including a literature synthesis of SOC change across maize-based systems in SSA. We found that nitrogen application reduced SOC loss, likely through increased biomass yield and consequently belowground carbon allocation. Residue return switched the direction of SOC change from loss to gain; such a benefit (SOC sequestration) was not compromised by CH₄ emissions (negligible) nor outweighed by the amplified N₂O emissions, and contributed to negative net GWP. Overall, we show encouraging results that, combining residue and fertilizer-nitrogen input allowed for sequestering 82–284 kg of CO₂-eq per Mg of maize grain produced across two soils. All analyses pointed to an advantage of sandy over clayey soils in achieving higher SOC sequestration targets, and thus call for a re-evaluation on the potential of sandy soils in SOC sequestration across SSA croplands. Our findings carry important implications for developing viable intensification practices for SSA croplands in mitigating climate change while securing food production.     

Soil GHG fluxes are altered by N deposition: New data indicate lower N stimulation of the N2O flux and greater stimulation of the calculated C pools

The effects of nitrogen (N) deposition on soil organic carbon (C) and greenhouse gas (GHG) emissions in terrestrial ecosystems are the main drivers affecting GHG budgets under global climate change. Although many studies have been conducted on this topic, we still have little understanding of how N deposition affects soil C pools and GHG budgets at the global scale. We synthesized a comprehensive dataset of 275 sites from multiple terrestrial ecosystems around the world and quantified the responses of the global soil C pool and GHG fluxes induced by N enrichment. The results showed that the soil organic C concentration and the soil CO₂, CH₄ and N₂O emissions increased by an average of 3.7%, 0.3%, 24.3% and 91.3% under N enrichment, respectively, and that the soil CH₄ uptake decreased by 6.0%. Furthermore, the percentage increase in N₂O emissions (91.3%) was two times lower than that (215%) reported by Liu and Greaver (Ecology Letters, 2009, 12:1103–1117). There was also greater stimulation of soil C pools (15.70 kg C ha^?1 year^?1 per kg N ha^?1 year^?1) than previously reported under N deposition globally. The global N deposition results showed that croplands were the largest GHG sources (calculated as CO₂ equivalents), followed by wetlands. However, forests and grasslands were two important GHG sinks. Globally, N deposition increased the terrestrial soil C sink by 6.34 Pg CO₂/year. It also increased net soil GHG emissions by 10.20 Pg CO₂‐Geq (CO₂ equivalents)/year. Therefore, N deposition not only increased the size of the soil C pool but also increased global GHG emissions, as calculated by the global warming potential approach.     

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.     

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.     

Greenhouse gas fluxes over managed grasslands in Central Europe

Central European grasslands are characterized by a wide range of different management practices in close geographical proximity. Site‐specific management strategies strongly affect the biosphere–atmosphere exchange of the three greenhouse gases (GHG) carbon dioxide (CO₂), nitrous oxide (N₂O), and methane (CH₄). The evaluation of environmental impacts at site level is challenging, because most in situ measurements focus on the quantification of CO₂ exchange, while long‐term N₂O and CH₄ flux measurements at ecosystem scale remain scarce. Here, we synthesized ecosystem CO₂, N₂O, and CH₄ fluxes from 14 managed grassland sites, quantified by eddy covariance or chamber techniques. We found that grasslands were on average a CO₂ sink (−1,783 to −91 g CO₂ m⁻² year⁻¹), but a N₂O source (18–638 g CO₂‐eq. m⁻² year⁻¹), and either a CH₄ sink or source (−9 to 488 g CO₂‐eq. m⁻² year⁻¹). The net GHG balance (NGB) of nine sites where measurements of all three GHGs were available was found between −2,761 and −58 g CO₂‐eq. m⁻² year⁻¹, with N₂O and CH₄ emissions offsetting concurrent CO₂ uptake by on average 21 ± 6% across sites. The only positive NGB was found for one site during a restoration year with ploughing. The predictive power of soil parameters for N₂O and CH₄ fluxes was generally low and varied considerably within years. However, after site‐specific data normalization, we identified environmental conditions that indicated enhanced GHG source/sink activity (“sweet spots”) and gave a good prediction of normalized overall fluxes across sites. The application of animal slurry to grasslands increased N₂O and CH₄ emissions. The N₂O‐N emission factor across sites was 1.8 ± 0.5%, but varied considerably at site level among the years (0.1%–8.6%). Although grassland management led to increased N₂O and CH₄ emissions, the CO₂ sink strength was generally the most dominant component of the annual GHG budget.     

Dynamics of soil biogeochemical gas emissions shaped by remolded aggregate sizes and carbon configurations under hydration cycles

Changes in soil hydration status affect microbial community dynamics and shape key biogeochemical processes. Evidence suggests that local anoxic conditions may persist and support anaerobic microbial activity in soil aggregates (or in similar hot spots) long after the bulk soil becomes aerated. To facilitate systematic studies of interactions among environmental factors with biogeochemical emissions of CO₂, N₂O and CH₄ from soil aggregates, we remolded silt soil aggregates to different sizes and incorporated carbon at different configurations (core, mixed, no addition). Assemblies of remolded soil aggregates of three sizes (18, 12, and 6 mm) and equal volumetric proportions were embedded in sand columns at four distinct layers. The water table level in each column varied periodically while obtaining measurements of soil GHG emissions for the different aggregate carbon configurations. Experimental results illustrate that methane production required prolonged inundation and highly anoxic conditions for inducing measurable fluxes. The onset of unsaturated conditions (lowering water table) resulted in a decrease in CH₄ emissions while temporarily increasing N₂O fluxes. Interestingly, N₂O fluxes were about 80% higher form aggregates with carbon placement in center (anoxic) core compared to mixed carbon within aggregates. The fluxes of CO₂ were comparable for both scenarios of carbon sources. These experimental results highlight the importance of hydration dynamics in activating different GHG production and affecting various transport mechanisms about 80% of total methane emissions during lowering water table level are attributed to physical storage (rather than production), whereas CO₂ emissions (~80%) are attributed to biological activity. A biophysical model for microbial activity within soil aggregates and profiles provides a means for results interpretation and prediction of trends within natural soils under a wide range of conditions.     

Conversion of coastal wetlands,riparian wetlands,and peatlands increases greenhouse gas emissions: A global meta‐analysis

Land‐use/land‐cover change (LULCC) often results in degradation of natural wetlands and affects the dynamics of greenhouse gases (GHGs). However, the magnitude of changes in GHG emissions from wetlands undergoing various LULCC types remains unclear. We conducted a global meta‐analysis with a database of 209 sites to examine the effects of LULCC types of constructed wetlands (CWs), croplands (CLs), aquaculture ponds (APs), drained wetlands (DWs), and pastures (PASs) on the variability in CO₂, CH₄, and N₂O emissions from the natural coastal wetlands, riparian wetlands, and peatlands. Our results showed that the natural wetlands were net sinks of atmospheric CO₂ and net sources of CH₄ and N₂O, exhibiting the capacity to mitigate greenhouse effects due to negative comprehensive global warming potentials (GWPs; ?0.9 to ?8.7 t CO₂‐eq ha^?1 year^?1). Relative to the natural wetlands, all LULCC types (except CWs from coastal wetlands) decreased the net CO₂ uptake by 69.7%?456.6%, due to a higher increase in ecosystem respiration relative to slight changes in gross primary production. The CWs and APs significantly increased the CH₄ emissions compared to those of the coastal wetlands. All LULCC types associated with the riparian wetlands significantly decreased the CH₄ emissions. When the peatlands were converted to the PASs, the CH₄ emissions significantly increased. The CLs, as well as DWs from peatlands, significantly increased the N₂O emissions in the natural wetlands. As a result, all LULCC types (except PASs from riparian wetlands) led to remarkably higher GWPs by 65.4%?2,948.8%, compared to those of the natural wetlands. The variability in GHG fluxes with LULCC was mainly sensitive to changes in soil water content, water table, salinity, soil nitrogen content, soil pH, and bulk density. This study highlights the significant role of LULCC in increasing comprehensive GHG emissions from global natural wetlands, and our results are useful for improving future models and manipulative experiments.