CO<Subscript>2</Subscript> Emission and Organic Carbon Pools in Soils of the Northern Taiga Ecosystems of Western Siberia under Different Geocryological Conditions

Statistical analysis of a vast body of data collected during five field seasons (2011–2015) was performed to characterize the biological activity of soils in the northern taiga ecosystems of Western Siberia. Automorphic forest soils, hydromorphic (oligotrophic bog) soils, and semihydromorphic (flat-topped and large peat mounds) soils were characterized. Statistically significant differences of average levels of CO₂ emission from the soils were identified at the ecosystem level. The CO₂ emission from podzols of automorphic forest ecosystems at the peak of the growing season (205 ± 30 to 410 ± 40 mg CO₂/(m² h)) was significantly higher than the emission from semihydromorphic soils of peat mounds (70 ± 20 to 116 ± 10 mg CO₂/(m² h)). The presence and depth of permafrost was a significant factor that affected ecosystem diversity and biological activity of northern taiga soils. Statistically significant differences in the total, labile, and microbial carbon pools were observed for the studied soils. Labile and microbial carbon pools in the organic layer (10 cm) of forest podzols amounted to 0.19 and 0.66 t/ha, respectively; those in the organic layer (40 cm) of peat cryozems of flat-topped peat mounds reached 1.24 and 3.20 t/ha, and those in the oligotrophic peat soils (50 cm) of large peat mounds were 2.76 and 1.35 t/ha, respectively. The portion of microbial carbon in the total carbon pool (C_micr/C_tot, %) varied significantly; according to the values of this index, the soils were arranged into the following sequence: oligotrophic peat soil < peat cryozem < podzol.     

The contribution of stone cover to biological activity in the Negev desert,Israel

Ancient valley agriculture in the northern Negev highlands was based on the principle of directed collection of water and eroded material from the slopes and their consequent flow towards the valleys. The stones on these slopes were therefore removed and/or collected into piles known as ‘grape mounds’. The aim of this study was to understand the contribution of stone cover and slope‐facing to biological activity in soil. Soil samples from a depth of 0–5 mm from the soil surface were collected during the study period (December 1994–March 1996) from northern and southern hill slopes, from under limestones and between stones. Soil moisture, organic matter, chlorophyll‐a and soil respiration were determined. The results obtained in field and laboratory studies demonstrated differences between the northern and southern slopes. The stone cover on the northern slope made up 33 per cent and in the southern slope 23 per cent, stone size ranging from 15–50 cm² and 15–35 cm², respectively. Soil moisture content varied from 12 per cent in December 1994 on both slopes to one‐quarter of the initial value during the dry period. Organic matter content reached a maximal level of 14 per cent and 16 per cent on the northern and southern slopes, respectively. Values of chlorophyll‐a on both the northern and southern slopes were 0.38 μg g⁻¹ dry soil during the wet season, decreasing to 0.05 μg g⁻¹ dry soil during the dry period. Soil samples from under the stones on both slopes produced high levels of CO₂, ranging between 50 and 100 μg CO₂ g;⁻¹ dry soil h⁻¹, whereas in the control samples the levels ranged between 30 and 70 μg CO₂ g⁻¹ dry soil h⁻¹. In conclusion, the stone cover apparently plays an important role in the maintenance of biological activity through its contribution to slope biotope stability. Copyright © 2001 John Wiley & Sons, Ltd.     

Soil chemistry versus environmental controls on production of CH4 and CO2 in northern peatlands

Rates of organic carbon mineralization (to CO₂ and CH₄) vary widely in peat soil. We transplanted four peat soils with different chemical composition into six sites with different environmental conditions to help resolve the debate about control of organic carbon mineralization by resource availability (e.g. carbon and nutrient chemistry) versus environmental conditions (e.g. temperature, moisture, pH). The four peat soils were derived from Sphagnum (bog moss). Two transplant sites were in mid‐boreal Alberta, Canada, two were in low‐boreal Ontario, Canada, and two were in the temperate United States. After 3 years in the field, CH₄ production varied significantly as a function of peat type, transplant site, and the type–site interaction. All four peat soils had very small rates of CH₄ production (< 20 nmol g^?1 day^?1) after transplant into two sites, presumably caused by acid site conditions (pH < 4.0). One peat soil had small CH₄ production rates regardless of transplant site. A canonical discriminant analysis revealed that large rates of CH₄ production (4000 nmol g^?1 day^?1) correlated with large holocellulose content, a large concentration of p‐hydroxyl phenolic compounds in the Klason lignin, and small concentrations of N, Ca and Mn in peat. Significant variation in rates of CO₂ production correlated positively with holocellulose content and negatively with N concentrations, regardless of transplant site. The temperature response for CO₂ production varied as a function of climate, being greater for peat formed in a cold climate, but did not apply to transplanted peat. Although we succeeded in elucidating some aspects of peat chemistry controlling production of CH₄ and CO₂ in Sphagnum‐derived peat soils, we also revealed idiosyncratic combinations of peat chemistry and site conditions that will complicate forecasting rates of peat carbon mineralization into the future.     

Respiration of Louisiana Freshwater Floating Marsh Soils Amended with Ammonium,Phosphate, and Sulfate

Wetland soils of the freshwater coastal deltaic regions of Louisiana have developed under decreasing influence from the Mississippi River, which has resulted in lower available nutrient conditions and sediment input relative to other coastal marshes. A laboratory soil respiration experiment was conducted to measure cumulative carbon dioxide (CO₂) and methane (CH₄) production in soils from a floating freshwater marsh in response to additions of added ammonium (N), phosphate (P), ammonium (N) + phosphate (P), and sulfate (S). CO₂ respiration was significantly greater over a 28-day period than controls following ammonium N, phosphorus, and sulfate addition at 10 mg L^?1. Nitrogen and phosphorus addition at 10 mg L^?1 also increased methane production. The lower sulfate amendment (10 mg L^?1) did not significantly increase CH₄ production. In contrast, the greatest sulfate treatment (100 m l^?1) significantly reduced total carbon (C) production by inhibiting CH₄ production. The fact that soil C/N (20.2) and C/P (355) ratios were both relatively low may partially explain why both N and P colimited microbial activity and respiration. While microbial activity of freshwater floating marsh soils was stimulated over the short term with increased ammonium, nitrogen, phosphorus, and sulfate exposure, it is unclear whether the increase would be the same over extended periods or would increase in plant productivity from nutrient additions compensate for any loss in soil carbon.     

Production,oxidation, emission and consumption of methane by soils: A review

Methane emission by soils results from antagonistic but correlated microbial activities. Methane is produced in the anaerobic zones of submerged soils by methanogens and is oxidised into CO₂ by methanotrophs in the aerobic zones of wetland soils and in upland soils. Methanogens and methanotrophs are ubiquitous in soils where they remain viable under unfavourable conditions. Methane transfer from the soil to the atmosphere occurs mostly through the aerenchyma of aquatic plants, but also by diffusion and as bubbles escaping from wetland soils. Methane sources are mainly wetlands. However 60 to more than 90 % of CH₄ produced in the anaerobic zones of wetlands is reoxidised in their aerobic zones (rhizosphere and oxidised soil-water interface). Methane consumption occurs in most soils and exhibits a broad range of values. Highest consumption rates or potentials are observed in soils where methanogenesis is or has been effective and where CH₄ concentration is or has been much higher than in the atmosphere (ricefields, swamps, landfills, etc.). Aerobic soils consume atmospheric CH₄ but their activities are very low and the micro-organisms involved are largely unknown. Methane emissions by cultivated or natural wetlands are expressed in mg CH₄·m^–2·h^–1 with a median lower than 10 mg CH₄·m^–2·h^–1. Methanotrophy in wetlands is most often expressed with the same unit. Methane oxidation by aerobic upland soils is rarely higher than 0.1 mg CH₄·m^–2·h^–1. Forest soils are the most active, followed by grasslands and cultivated soils. Factors that favour CH₄ emission from cultivated wetlands are mostly submersion and organic matter addition. Intermittent drainage and utilisation of the sulphate forms of N-fertilisers reduce CH₄ emission. Methane oxidation potential of upland soils is reduced by cultivation, especially by ammonium N-fertiliser application.     

Spatial Variability of Carbon Dioxide Emission by Soils in the Main Types of Forest Ecosystems at the Zvenigorod Biological Station of Moscow State University

Carbon dioxide (CO₂) emission from the soil surface in forest biogeocenoses of the Zvenigorod Biological Station of Moscow State University in summer varies on average from 120 to 350 mg C–CO₂/(m² h) and depends on the hydrothermal conditions (soil moisture and temperature) and the type of phytocenosis. The intensity of CO₂ emission in the biogeocenosis does not depend on its parcel structure and varies with respect to plant microgroups: it is maximum in oxalis pine–spruce and maple–lime forests and bracken spruce–birch forests and minimum in areas of forest fall without vegetation. The upper (from 0 to 20 cm thick) soil layer provides up to 50% of the total soil CO₂ emission. The role of microbial respiration in the total CO₂ emission from soils is determined by weather conditions and varies from 9–33% in a dry summer to 55–75% in a summer with favorable temperature and moisture.     

Microbial CO2 production, CH4 dynamics and nitrogen in a wetland soil (New York State, USA) associated with three plant species (Typha, Lythrum, Phalaris)

Plants furnish soil with organic carbon (OC) compounds that fuel soil microorganisms, but whether individual plant species – or plants with unique traits – do so uniquely is uncertain. We evaluated soil microbial processes within a wetland in which areas dominated by a distinct plant species (cattail –Typha sp.; purple loosestrife –Lythrum salicaria L.; reed canarygrass –Phalaris arundinacea L.) co‐mingled. We also established an experimental plot with plant shoot removal. The Phalaris area had more acidic soil pH (7.08 vs. 7.27–7.57), greater amount of soil organic matter (19.0% vs. 9.0–11.5%), and the slowest production rates of CO₂ (0.10 vs. 0.21–0.46 μmol kg⁻¹ s⁻¹) and CH₄ (0.040 vs. 0.054–0.079 nmol kg⁻¹ s⁻¹). Nitrogen cycling was dominated by net nitrification, with similar rates (17.2–18.9 mg kg⁻¹ 14 days⁻¹) among the four sampling areas. In the second part of the study, we emplaced soil cores that either allowed root in‐growth or excluded roots to evaluate how roots directly affect soil CO₂ and CH₄. The three plant species had similar amounts of root growth (ca 290 g m⁻² year⁻¹). Fungal biomass was similar in soils with root in‐growth versus root exclusion, regardless of dominant plant species. Rates of soil CO₂ production did not differ with root in‐growth versus root exclusion, and added glucose increased CO₂ production rates by only 35%. Root in‐growth did lead to greater rates of CH₄ production; albeit, addition of glucose had much greater effect on CH₄ production (1.24 nmol kg⁻¹ s⁻¹) compared with controls without added glucose (0.058 nmol kg⁻¹ s⁻¹). Our data revealed relatively few subtle differences in soil characteristics and processes associated with different plant species; albeit, roots had little effect, even inhibiting some microbial processes. This research highlights the need for both field and experimental studies in long‐established monocultures of plant species to understand the role of plant biodiversity in soil function.     

Microbial biomass and biological activity of soils and soil-like bodies in coastal oases of Antarctica

The method of luminescent microscopy has been applied to study the structure of the microbial biomass of soils and soil-like bodies in East (the Thala Hills and Larsemann Hills oases) and West (Cape Burks, Hobbs coast) Antarctica. According to Soil Taxonomy, the studied soils mainly belong to the subgroups of Aquic Haploturbels, Typic Haploturbels, Typic Haplorthels, and Lithic Haplorthels. The major contribution to their microbial biomass belongs to fungi. The highest fungal biomass (up to 790 μg C/g soil) has been found in the soils with surface organic horizons in the form of thin moss/lichen litters, in which the development of fungal mycelium is most active. A larger part of fungal biomass (70–98%) is represented by spores. For the soils without vegetation cover, the accumulation of bacterial and fungal biomass takes place in the horizons under surface desert pavements. In the upper parts of the soils without vegetation cover and in the organic soil horizons, the major part (>60%) of fungal mycelium contains protective melanin pigments. Among bacteria, the high portion (up to 50%) of small filtering forms is observed. A considerable increase (up to 290.2 ± 27 μg C/g soil) in the fungal biomass owing to the development of yeasts has been shown for gley soils (gleyzems) developing from sapropel sediments under subaquatic conditions and for the algal–bacterial mat on the bottom of the lake (920.7 ± 46 μg C/g soil). The production of carbon dioxide by the soils varies from 0.47 to 2.34 μg C–CO₂/(g day). The intensity of nitrogen fixation in the studied samples is generally low: from 0.08 to 55.85 ng С₂Н₄/(g day). The intensity of denitrification varies from 0.09 to 19.28 μg N–N₂O/(g day).     

Abiotic uptake of gases by organic soils

Methodological and experimental studies of the abiotic uptake of gaseous substances by organic soils were performed. The static adsorption method of closed vessels for assessing the interaction of gases with the solid and liquid soil phases and the dynamic method of determining the sorption isotherms of gases by soils were analyzed. The theoretical substantiation of the methods and their practical implementations on the basis of a PGA-7 portable gas analyzer (Russia) were considered. Good agreement between the equilibrium sorption isotherms of the gases and the Langmuir model was revealed; for the real ranges of natural gas concentrations, this model can be reduced to the linear Henry equation. The limit values of the gas sorption (Langmuir monolayer capacity) are typical for dry samples; they vary from 670–4000 g/m³ for methane and oxygen to 20 000–25 000 g/m³ for carbon dioxide. The linear distribution coefficients of gases between the solid and gas phases of organic soils (Henry constants) are 8–18 units for poorly sorbed gases (O₂, CH₄) and 40–60 units for CO₂. The kinetics of the chemicophysical uptake of gases by the soil studied is linear in character and obeys the relaxation kinetic model of the first order with the corresponding relaxation constants, which vary from 1 h ^?1 in wet samples to 10 h ^?1 in dry samples.     

Suppressing methane emission and global warming potential from rice fields through intermittent drainage and green biomass amendment

Winter cover crops are recommended to improve soil quality and carbon sequestration, although their use as green manure can significantly increase methane (CH₄) emission from paddy soils. Soil management practices can be used to reduce CH₄ emission from paddy soils, but intermittent drainage is regarded as a key practice to reduce CH₄ emission and global warming potential (GWP). However, significantly greater emissions of carbon dioxide (CO₂) and nitrous oxide (N₂O) are expected when large amounts of cover crop biomass are incorporated into soils. In this study, we investigated the effects of midseason drainage on CH₄ emission and GWP following incorporation of 0, 3, 6 and 12 Mg/ha of cover crop biomass. Methane, CO₂ and N₂O emission rates significantly (P < 0.05) increased with higher rates of cover crop biomass incorporation under both irrigation conditions. However, intermittent drainage effectively reduced seasonal CH₄ fluxes by ca. 42–46% and GWP by 17–31% compared to continuous flooding. Moreover, there were no significant differences in rice yield between the two water management practices with similar biomass incorporation rates. In conclusion, intermittent drainage and incorporation of 3 Mg/ha of green biomass could be a good management option to reduce GWP.     

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.     

Methane and nitrous oxide fluxes, and carbon dioxide production in boreal forest soil fertilized with wood ash and nitrogen

Wood ash has been used to alleviate nutrient deficiencies and acidification in boreal forest soils. However, ash and nitrogen (N) fertilization may affect microbial processes producing or consuming greenhouse gases: methane (CH₄), nitrous oxide (N₂O) and carbon dioxide (CO₂). Ash and N fertilization can stimulate nitrification and denitrification and, therefore, increase N₂O emission and suppress CH₄ uptake rate. Ash may also stimulate microbial respiration thereby enhancing CO₂ emission. The fluxes of CH₄, N₂O and CO₂ were measured in a boreal spruce forest soil treated with wood ash and/or N (ammonium nitrate) during three growing seasons. In addition to in situ measurements, CH₄ oxidation potential, CO₂ production, net nitrification and N₂O production were studied in laboratory incubations. The mean in situ N₂O emissions and in situ CO₂ production from the untreated, N, ash and ash + N treatments were not significantly different, ranging from 11 to 17 μg N₂O m^?2 h^?1 and from 533 to 611 mg CO₂ m^?2 h^?1. However, ash increased the CH₄ oxidation in a forest soil profile which could be seen both in the laboratory experiments and in the CH₄ uptake rates in situ. The mean in situ CH₄ uptake rate in the untreated, N, ash and ash + N plots were 153 ± 5, 123 ± 8, 188 ± 10 and 178 ± 18 μg m^?2 h^?1, respectively.     

Atmospheric Nitrogen Deposition and the Properties of Soils in Forests of Vologda Region

Twenty plots (20 m² each) were selected in coniferous and mixed forests of the industrial Vologda district and the Vytegra district without developed industries in Vologda region. In March, snow cores corresponding to the snow cover depth were taken on these plots. In August, soil samples from the 0- to 20-cm layer of litter-free soddy-podzolic soil (Albic Retisol (Ochric)) were taken on the same plots in August. The content of mineral nitrogen (N_min), including its ammonium (NH⁺₄) and nitrate (NO^-₃) forms, was determined in the snow (meltwater) and soil. The contents of total organic carbon, total nitrogen, and elements (Al, Ca); pH; particle size distribution; and microbiological parameters―carbon of microbial biomass (C_mic) and microbial respiration (MR)―were determined in the soil. The ratio MR/C_mic = qCO₂ (specific respiration of microbial biomass, or soil microbial metabolic quotient) was calculated. The content of N_mic in meltwater of two districts was 1.7 mg/L on the average (1.5 and 0.3 mg/L for the NH⁺₄ and NO^–₃ forms, respectively). The annual atmospheric deposition was 0.6–8.9 kg N_min/ha, the value of which in the Vologda district was higher than in the Vytegra district by 40%. Reliable correlations were found between atmospheric NH⁺₄ depositions and C_mic (–0.45), between NH⁺₄ and qCO₂ (0.56), between atmospheric NO^-₃ depositions and the soil NO^-₃ (–0.45), and between NO^-₃ and qCO₂ (–0.58). The content of atmospheric N_min depositions correlated with the ratios C/N (–0.46) and Al/Ca (–0.52) in the soil. In forests with the high input of atmospheric nitrogen (>2.0 kg NH⁺₄/(ha yr) and >6.4 kg N_min/(ha yr)), a tendency of decreasing C_mic, C/N, and Al/Ca, as well as increasing qCO₂, was revealed, which could be indicative of deterioration in the functioning of microbial community and the chemical properties of the soil.     

Net fluxes of CO2, but not N2O or CH4, are affected following agronomic-scale additions of urea to prairie and arable soils

While experimental addition of nitrogen (N) tends to enhance soil fluxes of carbon dioxide (CO₂), methane (CH₄), and nitrous oxide (N₂O), it is not known if lower and agronomic-scale additions of urea-N applied also enhance trace gas fluxes, particularly for semi-arid agricultural lands in the northern plains. We aimed to test if this were true at agronomic rates [low (11 kg N ha⁻¹), moderate (56 kg N ha⁻¹), and high (112 kg N ha⁻¹)] for central North Dakota arable and prairie soils using intact soil cores to minimize disturbance and simulate field conditions. Additions of urea to cores incubated at 21 °C and 57% water-filled pore space enhanced fluxes of CO₂ but not CH₄ and N₂O. At low, moderate, and high urea-N, CO₂ fluxes were significantly greater than control but not fluxes of CH₄ and N₂O. The increases in CO₂ emission with rate of urea-N application indicate that agronomic-scale N inputs may stimulate microbial carbon cycling in these soils, and that the contribution of CO₂ to net greenhouse gas source strength following fertilization of semi-arid agroecosystems may at times be greater than contributions by N₂O and CH₄.     

The differential effects of ammonium and nitrate on methanotrophs in rice field soil

It has been known that nitrogenous fertilizers can either stimulate or inhibit methane oxidation in soils. The mechanism, however, remains unclear. Here we conducted laboratory incubation experiments to evaluate the effects of ammonium versus nitrate amendment on CH₄ oxidation in a rice field soil. The results showed that both N forms stimulated CH₄ oxidation. But nitrate stimulated CH₄ oxidation to a greater extent than ammonium per unit N base. The 16S rRNA genes and the pmoA genes were analyzed to determine the dynamics of total bacterial and methanotrophic populations, respectively. The methanotrophic community consisted of type I and type II methanotrophs and was dominated by type I group after two weeks of incubation. Nitrate promoted both types of methanotrophs, but ammonium promoted only type I. DNA-based stable isotope probing confirmed that ammonium stimulated the incorporation of ¹³CH₄ into type I methanotrophs but not type II, while nitrate caused almost homogenous distribution of ¹³CH₄ in type I and type II methanotrophs. Our study suggests that nitrate can promote CH₄ oxidation more significantly than ammonium and is probably a better N source for both types of methanotrophs in rice field soil. More investigations, e.g. using ¹⁵N labeling, are necessary to elucidate this possibility.     

CO<Subscript>2</Subscript> emission from the surface of dark gray forest soils of the forest steppe and sandy soddy-podzolic soils of the southern taiga

Studies performed on dark gray loamy forest soils in an oak forest in the southern forest steppe and on sandy soddy-podzolic soil in a pine forest in the southern taiga showed that the annual emission of CO₂ from the soil surface in the pine forest was 16.3 t CO₂/ha, including 10.1 t CO₂/ha due to root respiration and 6.2 t CO₂/ha due to soil microbial respiration. In the southern forest steppe, the corresponding values were 17.8 t CO₂/ha due to root respiration at the optimum water content (20%) and 28.3 t CO₂/ha due to soil microbial respiration. With the insufficient soil water content (12.5%), 10.3 and 17.8 t CO₂/ha were due to root respiration and soil microbial respiration, respectively. Under strong drought conditions (water content of 10%), the emission of CO₂ decreased to 8.2 and 16.3 t/ha due to root respiration and soil microbial respiration, respectively.     

Methane emissions from paddy fields in Bali Island,Indonesia

Abstract

Methane emission rates from plots with and without fertilizer and rice straw application, and growth of two rice varieties (an improved variety, IR74 or IR64, and a local variety, Krueng Aceh) in two Indonesian paddy fields (Inceptisol and Alfisol soils of volcanic ash origin) were measured every week throughout the growth period in the first and the second cropping seasons, 1994. The CH₄ emission rates from the fields were similar between the two varieties. The effect of chemical fertilizer on the increase of the emissions was observed only in the Tabanan paddy field for the plots treated with rice straw. Application of rice straw increased the CH₄ emission rates. The mean rates of CH₄ emission were 1.37-2.13 mg CH₄?C m^?2 h^?1 for the plots without rice straw and 2.14–3.62 mg CH₄?C m^?2 h^?1 for the plots with rice straw application in the Alfisol plots, and 2.32–3.32 mg CH₄ -C m-2 h-1 for the plots without rice straw and 4.18–6.35 mg CH₄?C m^?2 h^?1 for the plots with rice straw application in the Inceptisol plots, respectively. Total amounts of CH₄ emitted during the growth period were 3.9–6.8 and 2.6–3.3 g CH₄?C m^?2 for the Alfisol plots and 6.9–10.7 and 4.2–5.8 g CH₄?C m^?2 for the Inceptisol plots with and without rice straw application, respectively. These findings suggested that CH₄ emission from tropical paddy fields with soils of volcanic ash origin is low.     

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.     

Evaluation of organic carbon stocks and СО<Subscript>2</Subscript> fluxes in grasslands of Western Transbaikalia

The stocks of organic carbon and mean rates of the CO₂ emission during the growing season (May–September) and the entire year were estimated in a sequence of grass ecosystems along the transect encompassing chestnut and meadow-chestnut steppe soils, marsh and meadow alluvial soils, and a haloxerophytic community on a typical solonchak. The total stocks of organic carbon comprised 6.17–9.70 kg С/m² in steppe, 7.41–10.04 kg С/m² in floodplain, and 4.74 kg С/m² in haloxerophytic ecosystems. The portion of humus carbon in the upper 50-cm-thick soil layer comprised 79–92% of the total carbon stock. The mean daily CO₂ emission (С–CO₂/(m² day)) from alluvial soils was moderate (3.3–4.9) or low (1.5–2.5). The dependence of the CO₂ emission on the moistening of steppe soils, temperature of alluvial soils, and temperature and moistening of solonchak was revealed. In comparison with the CO₂ emission from the zonal chestnut soil, its mean values during the growing season and the entire year were 1.2 times higher for the meadowchestnut soil, 3.3 times higher for the marsh alluvial soil, 2.3 times higher for the meadow alluvial soil, and 1.7 times higher for the solonchak. The portion of the CO₂ emission beyond the growing season in the mean annual emission averaged 19.8–24.2% and depended on the type of grass ecosystem and on weather conditions of particular years. The sink of carbon in the grass ecosystems exceeded carbon emission, especially in the steppe ecosystems.     

Methane uptake in soils from Pinus radiata plantations, a reverting shrubland and adjacent pastures: Effects of land-use change, and soil texture, water and mineral nitrogen

Afforestation and reforestation of pastures are key land-use changes in New Zealand that help sequester carbon (C) to offset its carbon dioxide (CO₂) emissions under the Kyoto Protocol. However, relatively little attention has been given so far to associated changes in trace gas fluxes. Here, we measure methane (CH₄) fluxes and CO₂ production, as well as microbial C, nitrogen (N) and mineral-N, in intact, gradually dried (ca. 2 months at 20 °C) cores of a volcanic soil and a heavier textured, non-volcanic soil collected within plantations of Pinus radiata D. Don (pine) and adjacent permanent pastures. CH₄ fluxes and CO₂ production were also measured in cores of another volcanic soil under reverting shrubland (mainly Kunzea var. ericoides (A. Rich) J. Thompson) and an adjacent pasture. CH₄ uptake in the pine and shrubland cores of the volcanic soils at field capacity averaged about 35 and 14 μg CH₄-C m⁻² h⁻¹, respectively, and was significantly higher than in the pasture cores (about 21 and 6 μg CH₄-C m⁻² h⁻¹, respectively). In the non-volcanic soil, however, CH₄-C uptake was similar in most cores of the pine and pasture soils, averaging about 7-9 μg m⁻² h⁻¹, except in very wet samples. In contrast, rates of CO₂ production and microbial C and N concentrations were significantly lower under pine than under pasture. In the air-dry cores, microbial C and N had declined in the volcanic soil, but not in the non-volcanic soil; ammonium-N, and especially nitrate-N, had increased significantly in all samples. CH₄ uptake was, with few exceptions, not significantly influenced by initial concentrations of ammonium-N or nitrate-N, nor by their changes on air-drying. A combination of phospholipid fatty acid (PLFA) and stable isotope probing (SIP) analyses of only the pine and pasture soils showed that different methanotrophic communities were probably active in soils under the different vegetations. The C18 PLFAs (type II methanotrophs) predominated under pine and C16 PLFAs (type I methanotrophs) predominated under pasture. Overall, vegetation, soil texture, and water-filled pore space influenced CH₄-C uptake more than did soil mineral-N concentrations.