Dynamics of methanogenesis and methanotrophy in tropical paddy soils as influenced by elevated CO2 and temperature interaction

Response of methanogenesis and methanotrophy to elevated carbon dioxide (CO₂) could be affected by changes in soil moisture content and temperature. In soil microcosms contained in glass bottles and incubated under laboratory conditions, we assessed the impact of elevated CO₂ and temperature interactions on methanogenesis and methanotrophy in alluvial and laterite paddy soils of tropical origin. Soil samples were incubated at ambient (370 μmol mol⁻¹) and elevated (600 μmol mol⁻¹) CO₂ concentrations at 25, 35 and 45 °C under non-flooded and flooded conditions for 60 d. Under flooded condition, elevated CO₂ significantly increased methane (CH₄) production while under non-flooded condition, only marginal increase in CH₄ production was observed in both the soils studied and the increase was significantly enhanced by further rise in temperature. Increased methanogenesis as a result of elevated CO₂ and temperature interaction was mostly attributed to decreased soil redox potential, increased readily mineralizable carbon, and also noticeable stimulation of methanogenic bacterial population. In contrast to CH₄ production, CH₄ oxidation was consistently low under elevated CO₂ concentration and the decrease was significant with rise in temperature. The low affinity and high affinity CH₄ oxidation were faster under non-flooded condition as compared to flooded condition. Admittedly, decreased low and high affinity CH₄ oxidation as a result of elevated CO₂ and temperature interaction was related to unfavorable lower redox status of soil and the inhibition of CH₄-oxidizing bacterial population.     

Increased moisture and methanogenesis contribute to reduced methane oxidation in elevated CO2 soils

Awareness of global warming has stimulated research on environmental controls of soil methane (CH₄) consumption and the effects of increasing atmospheric carbon dioxide (CO₂) on the terrestrial CH₄ sink. In this study, factors impacting soil CH₄ consumption were investigated using laboratory incubations of soils collected at the Free Air Carbon Transfer and Storage I site in the Duke Forest, NC, where plots have been exposed to ambient (370 μL L⁻¹) or elevated (ambient + 200 μL L⁻¹) CO₂ since August 1996. Over 1 year, nearly 90% of the 360 incubations showed net CH₄ consumption, confirming that CH₄-oxidizing (methanotrophic) bacteria were active. Soil moisture was significantly (p < 0.01) higher in the 25–30 cm layer of elevated CO₂ soils over the length of the study, but soil moisture was equal between CO₂ treatments in shallower soils. The increased soil moisture corresponded to decreased net CH₄ oxidation, as elevated CO₂ soils also oxidized 70% less CH₄ at the 25–30 cm depth compared to ambient CO₂ soils, while CH₄ consumption was equal between treatments in shallower soils. Soil moisture content predicted (p < 0.05) CH₄ consumption in upper layers of ambient CO₂ soils, but this relationship was not significant in elevated CO₂ soils at any depth, suggesting that environmental factors in addition to moisture were influencing net CH₄ oxidation under elevated CO₂. More than 6% of the activity assays showed net CH₄ production, and of these, 80% contained soils from elevated CO₂ plots. In addition, more than 50% of the CH₄-producing flasks from elevated CO₂ sites contained deeper (25–30 cm) soils. These results indicate that subsurface (25 cm+) CH₄ production contributes to decreased net CH₄ consumption under elevated CO₂ in otherwise aerobic soils.     

Groundwater level controls CO2, N2O and CH4 fluxes of three different hydromorphic soil types of a temperate forest ecosystem

Hydromorphic soils should exhibit higher climate change feedback potentials than well aerated soils since soil organic matter (SOM) losses in them are predicted to be much larger than those of well aerated soils. To evaluate a combined feedback relationship between groundwater level (GWL) and total greenhouse gas (GHG) emission, a greenhouse microcosm experiment was performed by exposing three hydromorphic forest soil types that differed in carbon content to three water levels (?40, ?20 and ?5 cm) while plants were excluded. Net GHG fluxes were measured continuously. GHG concentrations plus oxygen were measured in soil air and soil water at different depths. In this study, soil type hardly affected GHG emissions but GWL did. CO₂ emissions peaked at GWL of ?40 cm and declined on average to 65 and 33% during GWL at ?20 and ?5 cm, respectively. CH₄ emissions showed the opposite pattern having the highest emission rates at GWL of ?5 cm and compared to that on average only ?3 and ?8% during GWL at ?20 and ?40 cm, respectively. The highest mean N₂O emissions were detected at the intermediate GWL of ?20 cm, whereas it is reduced on average to 18% for GWL at ?40 cm and at ?5 cm. The highest greenhouse gas emissions (in CO₂ equivalents) were calculated for GWL at ?20 cm. During GWL at ?40 cm, CO₂ equivalent fluxes were only insignificantly lower. CO₂ equivalent fluxes reduced explicitly in mean to 35% with GWL at ?5 cm. The outcome emphasizes that anaerobic SOM decomposition apparently produces a lower warming potential than aerobic SOM decomposition. Undoubtedly, hydromorphic soils have to be considered for climate–carbon feedback scenarios.     

Carbon dioxide, nitrous oxide and methane dynamics in boreal organic agricultural soils with different soil characteristics

The annual carbon dioxide (CO₂), nitrous oxide (N₂O) and methane (CH₄) dynamics were measured with static chambers on two organic agricultural soils with different soil characteristics. Site 1 had a peat layer of 30 cm, with an organic matter (OM) content of 74% in the top 20 cm. Site 2 had a peat layer of 70 cm but an OM content of only 40% in the top 20 cm. On both sites there were plots under barley and grass and also plots where the vegetation was removed. All soils were net sources of CO₂ and N₂O, but they consumed atmospheric CH₄. Soils under barley had higher net CO₂ emissions (830 g CO₂-C m⁻² yr⁻¹) and N₂O emissions (848 mg N₂O-N m⁻² yr⁻¹) than those under grass (395 g CO₂-C m⁻³ yr⁻¹ and 275 mg N₂O-N m⁻² yr⁻¹). Bare soils had the highest N₂O emissions, mean 2350 mg N₂O-N m⁻² yr⁻¹. The mean CH₄ uptake rate from vegetated soils was 100 mg CH₄-C m⁻³ yr⁻¹ and from bare soils 55 mg CH₄-C m⁻² yr⁻¹. The net CO₂ emissions were higher from Site 2, which had a high peat bulk density and a low OM content derived from the addition of mineral soil to the peat during the cultivation history of that site. Despite the differences in soil characteristics, the mean N₂O emissions were similar from vegetated peat soils from both sites. However, bare soils from Site 2 with mineral soil addition had N₂O emissions of 2-9 times greater than those from Site 1. Site 1 consumed atmospheric CH₄ at a higher rate than Site 2 with additional mineral soil. N₂O emissions during winter were an important component of the N₂O budget even though they varied greatly, ranging from 2 to 99% (mean 26%) of the annual emission.     

Dissolved organic matter and inorganic N jointly regulate greenhouse gases fluxes from forest soils with different moistures during a freeze-thaw period

ABSTRACT

Antecedent soil moisture before freezing can affect greenhouse gases (GHG) fluxes from soils during thaw, but their critical threshold values for GHG fluxes and the underlying mechanisms are still not clear. By using packed soil-core incubation experiments, we have studied nitrous oxide (N₂O), carbon dioxide (CO₂) and methane (CH₄) fluxes from a mature broadleaf and Korean pine-mixed forest soil and an adjacent white birch forest soil with nine levels of soil moisture ranging from 10 to 90% water-filled pore space (WFPS) during a 2-month freezing at ?8°C and the following 10-day thaw at 10°C. The threshold values of soil moisture ranged from 50 to 70% WFPS for CH₄ uptake and from 70 to 90% WFPS for N₂O and CO₂ emissions from the two soils during the freeze-thaw period. Under the optimum soil moisture condition, fulvic-like compounds with high bioavailability contributed more than 60% of dissolved organic matter (DOM) in the soil. Cumulative N₂O emissions from forest soils during the freeze-thaw period were greatest when the concentration ratio of nitrate-N to dissolved organic carbon (DOC) was 0.04 g N g^?1 C. Cumulative soil CO₂ emissions and CH₄ uptake during the freeze-thaw period were both regulated by the interaction between soil DOC and net N mineralization. The activities of β-1,4-glucosidase and β-1,4-N-acetyl-glucosaminidase, microbial biomass C and N, and the microbial biomass C-to-N ratios, were all significantly correlated to the soil N₂O, CO₂, and CH₄ fluxes. Overall, upon a freeze-thaw period with different soil moistures, GHG fluxes from forest soils were jointly regulated by inorganic N and DOC concentrations, and related to the labile components of DOM released into the soil, which could be strictly controlled by the related microbial properties.     

Methane production in a flooded soil in response to elevated atmospheric carbon dioxide concentrations

 CH₄ production in a flooded soil as affected by elevated atmospheric CO₂ was quantified in a laboratory incubation study. CH₄ production in the flooded soil increased by 19.6%, 28.2%, and 33.4% after a 2-week incubation and by 38.2%, 62.4%, and 43.0% after a 3-week incubation under atmospheres of 498, 820, and 1050 μl l^–1 CO₂, respectively, over that in soil under the ambient CO₂ concentration. CH₄ production in slurry under 690, 920, and 1150 μl l^–1 CO₂ increased by 2.7%, 5.5%, and 5.0%, respectively, after a 3-day incubation, and by 6.7%, 12.8%, and 5.4%, respectively, after a 6-day incubation over that in slurry under the ambient CO₂ concentration. The increase in CH₄ production in the soil slurry under elevated CO₂ concentrations in a N₂ atmosphere was more pronounced than that under elevated CO₂ concentrations in air. These data suggested that elevated atmospheric CO₂ concentrations could promote methanogenic activity in flooded soil. Received: 2 March 1998     

Exchange of greenhouse gases between soil and atmosphere: interactions of soil physical factors and biological processes

This review examines the interactions between soil physical factors and the biological processes responsible for the production and consumption in soils of greenhouse gases. The release of CO₂ by aerobic respiration is a non‐linear function of temperature over a wide range of soil water contents, but becomes a function of water content as a soil dries out. Some of the reported variation in the temperature response may be attributable simply to measurement procedures. Lowering the water table in organic soils by drainage increases the release of soil carbon as CO₂ in some but not all environments, and reduces the quantity of CH₄ emitted to the atmosphere. Ebullition and diffusion through the aerenchyma of rice and plants in natural wetlands both contribute substantially to the emission of CH₄; the proportion of the emissions taking place by each pathway varies seasonally. Aerated soils are a sink for atmospheric CH₄, through microbial oxidation. The main control on oxidation rate is gas diffusivity, and the temperature response is small. Nitrous oxide is the third greenhouse gas produced in soils, together with NO, a precursor of tropospheric ozone (a short‐lived greenhouse gas). Emission of N₂O increases markedly with increasing temperature, and this is attributed to increases in the anaerobic volume fraction, brought about by an increased respiratory sink for O₂. Increases in water‐filled pore space also result in increased anaerobic volume; again, the outcome is an exponential increase in N₂O emission. The review draws substantially on sources from beyond the normal range of soil science literature, and is intended to promote integration of ideas, not only between soil biology and soil physics, but also over a wider range of interacting disciplines.     

Influence of water table level and soil properties on emissions of greenhouse gases from cultivated peat soil

A lysimeter method using undisturbed soil columns was used to investigate the effect of water table depth and soil properties on soil organic matter decomposition and greenhouse gas (GHG) emissions from cultivated peat soils. The study was carried out using cultivated organic soils from two locations in Sweden: Örke, a typical cultivated fen peat with low pH and high organic matter content and Majnegården, a more uncommon fen peat type with high pH and low organic matter content. Even though carbon and nitrogen contents differ greatly between the sites, carbon and nitrogen density are quite similar. A drilling method with minimal soil disturbance was used to collect 12 undisturbed soil monoliths (50 cm high, Ø29.5 cm) per site. They were sown with ryegrass (Lolium perenne) after the original vegetation was removed. The lysimeter design allowed the introduction of water at depth so as to maintain a constant water table at either 40 cm or 80 cm below the soil surface. CO₂, CH₄ and N₂O emissions from the lysimeters were measured weekly and complemented with incubation experiments with small undisturbed soil cores subjected to different tensions (5, 40, 80 and 600 cm water column). CO₂ emissions were greater from the treatment with the high water table level (40 cm) compared with the low level (80 cm). N₂O emissions peaked in springtime and CH₄ emissions were very low or negative. Estimated GHG emissions during one year were between 2.70 and 3.55 kg CO₂ equivalents m⁻². The results from the incubation experiment were in agreement with emissions results from the lysimeter experiments. We attribute the observed differences in GHG emissions between the soils to the contrasting dry matter liability and soil physical properties. The properties of the different soil layers will determine the effect of water table regulation. Lowering the water table without exposing new layers with easily decomposable material would have a limited effect on emission rates.     

Degradability of black carbon and its impact on trace gas fluxes and carbon turnover in paddy soils

Rice paddy soils are characterized by anoxic conditions, anaerobic carbon turnover, and significant emissions of the greenhouse gas methane. A main source for soil organic matter in paddy fields is the rice crop residue that is returned to fields if not burned. We investigated as an alternative treatment the amendment of rice paddies with rice residues that have been charred to black carbon. This treatment might avoid various negative side effects of traditional rice residue treatments. Although charred biomass is seen as almost recalcitrant, its impact on trace gas (CO₂, CH₄) production and emissions in paddy fields has not been studied. We quantified the degradation of black carbon produced from rice husks in four wetland soils in laboratory incubations. In two of the studied soils the addition of carbonised rice husks resulted in a transient increase in carbon mineralisation rates in comparison to control soils without organic matter addition. After almost three years, between 4.4% and 8.5% of the black carbon added was mineralised to CO₂ under aerobic and anaerobic conditions, respectively. The addition of untreated rice husks resulted in a strong increase in carbon mineralisation rates and in the same time period 77%-100% of the added rice husks were mineralised aerobically and 31%-54% anaerobically. The ¹³C-signatures of respired CO₂ gave a direct indication of black carbon mineralisation to CO_2. In field trials we quantified the impact of rice husk black carbon or untreated rice husks on soil respiration and methane emissions. The application of black carbon had no significant effect on soil respiration but significantly enhanced methane emissions in the first rice crop season. The additional methane released accounted for only 0.14% of black carbon added. If the same amount of organic carbon was added as untreated rice husks, 34% of the applied carbon was released as CO₂ and methane in the first season. Furthermore, the addition of fresh harvest residues to paddy fields resulted in a disproportionally high increase in methane emissions. Estimating the carbon budget of the different rice crop residue treatments indicated that charring of rice residues and adding the obtained black carbon to paddy fields instead of incorporating untreated harvest residues may reduce field methane emissions by as much as 80%. Hence, the production of black carbon from rice harvest residues could be a powerful strategy for mitigating greenhouse gas emissions from rice fields.     

Total carbon and nitrogen in the soils of the world

The soil is important in sequestering atmospheric CO₂ and in emitting trace gases (e.g. CO₂, CH₄ and N₂O) that are radiatively active and enhance the ‘greenhouse’ effect. Land use changes and predicted global warming, through their effects on net primary productivity, the plant community and soil conditions, may have important effects on the size of the organic matter pool in the soil and directly affect the atmospheric concentration of these trace gases. A discrepancy of approximately 350 × 10¹⁵ g (or Pg) of C in two recent estimates of soil carbon reserves worldwide is evaluated using the geo-referenced database developed for the World Inventory of Soil Emission Potentials (WISE) project. This database holds 4353 soil profiles distributed globally which are considered to represent the soil units shown on a ¹/₂° latitude by ¹/₂° longitude version of the corrected and digitized 1:5 M FAO–UNESCO Soil Map of the World. Total soil carbon pools for the entire land area of the world, excluding carbon held in the litter layer and charcoal, amounts to 2157–2293 Pg of C in the upper 100 cm. Soil organic carbon is estimated to be 684–724 Pg of C in the upper 30 cm, 1462–1548 Pg of C in the upper 100 cm, and 2376–2456 Pg of C in the upper 200 cm. Although deforestation, changes in land use and predicted climate change can alter the amount of organic carbon held in the superficial soil layers rapidly, this is less so for the soil carbonate carbon. An estimated 695–748 Pg of carbonate-C is held in the upper 100 cm of the world's soils. Mean C: N ratios of soil organic matter range from 9.9 for arid Yermosols to 25.8 for Histosols. Global amounts of soil nitrogen are estimated to be 133–140 Pg of N for the upper 100 cm. Possible changes in soil organic carbon and nitrogen dynamics caused by increased concentrations of atmospheric CO₂ and the predicted associated rise in temperature are discussed.     

Soil organic matter dynamics in grassland soils under elevated CO2: Insights from long-term incubations and stable isotopes

Elevated atmospheric carbon dioxide (CO₂) levels generally stimulate carbon (C) uptake by plants, but the fate of this additional C largely remains unknown. This uncertainty is due in part to the difficulty in detecting small changes in soil carbon pools. We conducted a series of long-term (170-330 days) laboratory incubation experiments to examine changes in soil organic matter pool sizes and turnover rates in soil collected from an open-top chamber (OTC) elevated CO₂ study in Colorado shortgrass steppe. We measured concentration and isotopic composition of respired CO₂ and applied a two-pool exponential decay model to estimate pool sizes and turnover rates of active and slow C pools. The active and slow C pools of surface soils (5-10 cm depth) were increased by elevated CO₂, but turnover rates of these pools were not consistently altered. These findings indicate a potential for C accumulation in near-surface soil C pools under elevated CO₂. Stable isotopes provided evidence that elevated CO₂ did not alter the decomposition rate of new C inputs. Temporal variations in measured δ¹³C of respired CO₂ during incubation probably resulted mainly from the decomposition of changing mixtures of fresh residue and older organic matter. Lignin decomposition may have contributed to declining δ¹³C values late in the experiments. Isotopic dynamics during decomposition should be taken into account when interpreting δ¹³C measurements of soil respiration. Our study provides new understanding of soil C dynamics under elevated CO₂ through the use of stable C isotope measurements during microbial organic matter mineralization.     

Functional dependencies of soil CO2 emissions on soil biological properties in northern German agricultural soils derived from a glacial till

Agricultural soil CO₂ emissions and their controlling factors have recently received increased attention because of the high potential of carbon sequestration and their importance in soil fertility. Several parameters of soil structure, chemistry, and microbiology were monitored along with soil CO₂ emissions in research conducted in soils derived from a glacial till. The investigation was carried out during the 2012 growing season in Northern Germany. Higher potentials of soil CO₂ emissions were found in grassland (20.40 µg g^?1 dry weight h^?1) compared to arable land (5.59 µg g^?1 dry weight h^?1) within the incubating temperature from 5°C to 40°C and incubating moisture from 30% to 70% water holding capacity (WHC) of soils taken during the growing season. For agricultural soils regardless of pasture and arable management, we suggested nine key factors that influence changes in soil CO₂ emissions including soil temperature, metabolic quotient, bulk density, WHC, percentage of silt, bacterial biomass, pH, soil organic carbon, and hot water soluble carbon (glucose equivalent) based on principal component analysis and hierarchical cluster analysis. Slightly different key factors were proposed concerning individual land use types, however, the most important factors for soil CO₂ emissions of agricultural soils in Northern Germany were proved to be metabolic quotient and soil temperature. Our results are valuable in providing key influencing factors for soil CO₂ emission changes in grassland and arable land with respect to soil respiration, physical status, nutrition supply, and microbe-related parameters.     

Short-term effects of raw rice straw and its derived biochar on greenhouse gas emission in five typical soils in China

Abstract

A short-term study was conducted to investigate the greenhouse gas emissions in five typical soils under two crop residue management practices: raw rice straw (Oryza sativa L., cv) and its derived biochar application. Rice straw and its derived biochar (two biochars, produced at 350 and 500°C and referred to as BC350 and BC500, respectively) were incubated with the soils at a 5% (weight/weight) rate and under 70% water holding capacity for 28 d. Incorporation of BC500 into soils reduced carbon dioxide (CO₂) and nitrous oxide (N₂O) emission in all five soils by 4?40% and 62?98%, respectively, compared to the untreated soils, whereas methane (CH₄) emission was elevated by up to about 2 times. Contrary to the biochars, direct return of the straw to soil reduced CH₄ emission by 22?69%, whereas CO₂ increased by 4 to 34 times. For N₂O emission, return of rice straw to soil reduced it by over 80% in two soils, while it increased by up to 14 times in other three soils. When all three greenhouse gases were normalized on the CO₂ basis, the global warming potential in all treatments followed the order of straw > BC350 > control > BC500 in all five soils. The results indicated that turning rice straw into biochar followed by its incorporation into soil was an effective measure for reducing soil greenhouse gas emission, and the effectiveness increased with increasing biochar production temperature, whereas direct return of straw to soil enhanced soil greenhouse gas emissions.     

Effects of biochar application in forest ecosystems on soil properties and greenhouse gas emissions: a review

Purpose

Forests play a critical role in terrestrial ecosystem carbon cycling and the mitigation of global climate change. Intensive forest management and global climate change have had negative impacts on the quality of forest soils via soil acidification, reduction of soil organic carbon content, deterioration of soil biological properties, and reduction of soil biodiversity. The role of biochar in improving soil properties and the mitigation of greenhouse gas (GHG) emissions has been extensively documented in agricultural soils, while the effect of biochar application on forest soils remains poorly understood. Here, we review and summarize the available literature on the effects of biochar on soil properties and GHG emissions in forest soils.

Materials and methods

This review focuses on (1) the effect of biochar application on soil physical, chemical, and microbial properties in forest ecosystems; (2) the effect of biochar application on soil GHG emissions in forest ecosystems; and (3) knowledge gaps concerning the effect of biochar application on biogeochemical and ecological processes in forest soils.

Results and discussion

Biochar application to forests generally increases soil porosity, soil moisture retention, and aggregate stability while reducing soil bulk density. In addition, it typically enhances soil chemical properties including pH, organic carbon stock, cation exchange capacity, and the concentration of available phosphorous and potassium. Further, biochar application alters microbial community structure in forest soils, while the increase of soil microbial biomass is only a short-term effect of biochar application. Biochar effects on GHG emissions have been shown to be variable as reflected in significantly decreasing soil N₂O emissions, increasing soil CH₄ uptake, and complex (negative, positive, or negligible) changes of soil CO₂ emissions. Moreover, all of the aforementioned effects are biochar-, soil-, and plant-specific.

Conclusions

The application of biochars to forest soils generally results in the improvement of soil physical, chemical, and microbial properties while also mitigating soil GHG emissions. Therefore, we propose that the application of biochar in forest soils has considerable advantages, and this is especially true for plantation soils with low fertility.

     

Impact of the heatwave in 2003 on the summer CH4 budget of a spruce forest with large variation in soil drainage: A four‐year comparison (2001–2004)

Well‐aerated soils are sinks for atmospheric methane (CH₄) whereas hydromorphic soils act as sources. Both CH₄ oxidation and production are highly sensitive to variation in soil moisture. Significant changes of net CH₄ fluxes from soils can therefore be expected to accompany redistribution of precipitation in the course of climate change where more extreme events are predicted for the future. The extreme summer drought in 2003 offered the opportunity to study the impact of such events on methane fluxes under field conditions. The objective was to evaluate the impact of the summer drought in 2003 on net methane budget of a spruce‐forest ecosystem. We studied net CH₄ flux (bi‐)weekly during the summers of 2000–2004 using a closed‐chamber technique on six different soil types ranging from well‐aerated Cambisols, to poorly drained Gleysols and a wet Histosol in a cool‐humid spruce forest.     

Microcosm Study of Iron Mobilization and Greenhouse Gas Evolution in Soils of a Plantation-Forested Subtropical Coastal Catchment

This study examined the potential for Fe mobilization and greenhouse gas (GHG, e.g. CO₂, and CH₄) evolution in SEQ soils associated with a range of plantation forestry practices and water-logged conditions. Intact, 30-cm-deep soil cores collected from representative sites were saturated and incubated for 35?days in the laboratory, with leachate and headspace gas samples periodically collected. Minimal Fe dissolution was observed in well-drained sand soils associated with mature, first-rotation Pinus and organic Fe complexation, whereas progressive Fe dissolution occurred over 14?days in clear-felled and replanted Pinus soils with low organic matter and non-crystalline Fe fractions. Both CO₂ and CH₄ effluxes were relatively lower in clear-felled and replanted soils compared with mature, first-rotation Pinus soils, despite the lack of statistically significant variations in total GHG effluxes associated with different forestry practices. Fe dissolution and GHG evolution in low-lying, water-logged soils adjacent to riparian and estuarine, native-vegetation buffer zones were impacted by mineral and physical soil properties. Highest levels of dissolved Fe and GHG effluxes resulted from saturation of riparian loam soils with high Fe and clay content, as well as abundant organic material and Fe-metabolizing bacteria. Results indicate Pinus forestry practices such as clear-felling and replanting may elevate Fe mobilization while decreasing CO₂ and CH₄ emissions from well-drained, SEQ plantation soils upon heavy flooding. Prolonged water-logging accelerates bacterially mediated Fe cycling in low-lying, clay-rich soils, leading to substantial Fe dissolution, organic matter mineralization, and CH₄ production in riparian native-vegetation buffer zones.     

Strong pH influence on N2O and CH4 fluxes from forested organic soils

Greenhouse gas (GHG) emissions from farmed organic soils can have a major impact on national emission budgets. This investigation was conducted to evaluate whether afforestation of such soils could mitigate this problem. Over the period 1994–1997, emissions of methane (CH₄) and nitrous oxide (N₂O) were recorded from an organic soil site in Sweden, forested with silver birch (Betula pendula Roth), using static field chambers. The site was used for grazing prior to forestation. Soil pH and soil carbon content varied greatly across the site. The soil pH ranged from 3.6 to 5.9 and soil carbon from 34 to 42%. The mean annual N₂O emission was 19.4 (± 6.7) kg N₂O‐N ha^?1 and was strongly correlated with soil pH (r = ?0.93, P < 0.01) and soil carbon content (r = 0.97, P < 0.001). The N₂O emissions showed large spatial and temporal variability with greatest emissions during the summer periods. The site was a sink for CH₄ (i.e. ?0.8 (± 0.5) kg CH₄ ha^?1 year^?1) and the flux correlated well with the C/N ratio (r = 0.93, P < 0.01), N₂O emission (r = 0.92, P < 0.01), soil pH (r = ?0.95, P < 0.01) and soil carbon (r = 0.97, P < 0.001). CH₄ flux followed a seasonal pattern, with uptake dominating during the summer, and emission during winter. This study indicates that, because of the large N₂O emissions, afforestation may not mitigate the GHG emissions from fertile peat soils with acidic pH, although it can reduce the net GHG because of greater CO₂ assimilation by the trees compared with agricultural crops.     

Methane production potential and methanogenic archaeal community structure in tropical irrigated Indian paddy soils

Soil characteristics regulate various belowground microbial processes including methanogenesis and, consequently, affect the structure and function of methanogenic archaeal communities due to change in soil type which in turn influences the CH₄ production potential of soils. Thus, five different soil orders (Alfisol, Entisol, Inceptisol, Podzol and Vertisol) were studied to assess their CH₄ production potential and also the methanogenic archaeal community structure in dryland irrigated Indian paddy soils. Soil incubation experiments revealed CH₄ production to range from 178.4 to 431.2 μg CH₄ g^-1 dws in all soil orders as: Vertisol<Inceptisol<Entisol<Podzol<Alfisol. The numbers of methanogens as quantified using real-time quantitative polymerase chain reaction (qPCR) targeting mcrA genes varied between 0.06 and 72.97 (×10⁶ copies g^-1 dws) and were the highest in Vertisol soil and the least in Alfisol soil. PCR-denaturing gradient gel electrophoresis (DGGE)-based approach targeting 16S rRNA genes revealed diverse methanogenic archaeal communities across all soils. A total of 43 DGGE bands sequenced showed the closely related groups to Methanomicrobiaceae, Methanobacteriaceae, Methanocellales, Methanosarcinaceae, Methanosaetaceae and Crenarchaeota. The composition of methanogenic groups differed among all soils and only the Methanocellales group was common and dominant in all types of soils. The highest diversity of methanogens was found in Inceptisol and Vertisol soils. Methane production potential varied significantly in different soil orders with a positive relationship (p?<?0.05) with methanogens population size, permanganate oxidizable C (POXC) and CO₂ production. The present study suggested that CH₄ production potential of different soils depends on physicochemical properties, methanogenic archaeal community composition and the population size.     

Priming depletes soil carbon and releases nitrogen in a scrub-oak ecosystem exposed to elevated CO2

Elevated atmospheric CO₂ tends to stimulate plant productivity, which could either stimulate or suppress the processing of soil carbon, thereby feeding back to atmospheric CO₂ concentrations. We employed an acid-hydrolysis-incubation method and a net nitrogen-mineralization assay to assess stability of soil carbon pools and short-term nitrogen dynamics in a Florida scrub-oak ecosystem after six years of exposure to elevated CO₂. We found that soil carbon concentration in the slow pool was 27% lower in elevated than ambient CO₂ plots at 0-10 cm depth. The difference in carbon mass was equivalent to roughly one-third of the increase in plant biomass that occurred in the same experiment. These results concur with previous reports from this ecosystem that elevated CO₂ stimulates microbial degradation of relatively stable soil organic carbon pools. Accordingly, elevated CO₂ increased net N mineralization in the 10-30 cm depth, which may increase N availability, thereby allowing for continued stimulation of plant productivity by elevated CO₂. Our findings suggest that soil texture and climate may explain the differential response of soil carbon among various long-term, field-based CO₂ studies. Increased mineralization of stable soil organic carbon by a CO₂-induced priming effect may diminish the terrestrial carbon sink globally.     

Physical,chemical and microbiological soil attributes influence soil greenhouse gases fluxes in Atlantic Forest and pine (Pinus taeda) plantations in Brazil

Forest soils can be sources or sinks of greenhouse gases (GHGs) depending on soil attributes that affect biomass and activity of soil micro-organisms involved in GHGs fluxes. In this work, we tested the hypothesis that soil physical, chemical and microbiological attributes, under different forests ecosystems, affect the soil GHGs [nitrous oxide (N₂O), carbon dioxide (CO₂) and methane (CH₄)] fluxes. The study was carried out in two locations in southern Brazil in 2019, with three experimental plots of 900 m² in native forests of the Atlantic Forest biome and in loblolly pine (Pinus taeda) plantations. Air samples released from the soil surface were analysed for concentration and flux of CO₂, N₂O and CH₄. Soil samples were analysed for chemical attributes, density (Ds), soil microporosity (MiPs), soil macroporosity (MaPs), total porosity (TP), water-filled pore space (WFPS), microbial biomass carbon (MB-C), basal respiration (BR), microbial (qMic) and metabolic (qCO₂) quotient and activities of soil urease and β-glucosidase enzymes. The seasons influenced the CO₂ and N₂O emissions, probably because of the changes in seasonal conditions. However, native forests consumed more CH₄ than pine plantations. Meanwhile, the native forests presented soils with lower Ds (average 21.5% lower), more TP (average 12.5% higher) and more moisture (average 33% higher), which improved the microbiological attributes of the soil (20% to 60% more MB-C, 67% higher urease activity and 30% higher β-glucosidase activity) compared with pine plantations. Native forests contributed more intensely to CH₄ consumption than pine plantations because they present better physical, chemical and microbiological soil conditions. Therefore, it is possible that forestry practices that improve soil physical attributes are likely to contribute to increase CH₄ consumption, and to reduce GHGs emissions in forest ecosystems.