Carbon dioxide,methane, and nitrous oxide exchanges in an age‐sequence of temperate pine forests

We investigated soil carbon dioxide (CO₂), methane (CH₄), and nitrous oxide (N₂O) exchanges in an age‐sequence (4, 17, 32, 67 years old) of eastern white pine (Pinus strobus L.) forests in southern Ontario, Canada, for the period of mid‐April to mid‐December in 2006 and 2007. For both CH₄ and N₂O, we observed uptake and emission ranging from ?160 to 245 μg CH₄ m^?2 h^?1 and ?52 to 21 μg N₂O m^?2 h^?1, respectively (negative values indicate uptake). Mean fluxes from mid‐April to mid‐December across the 4, 17, 32, 67 years old stands were similar for CO₂ fluxes (259, 246, 220, and 250 mg CO₂ m^?2 h^?1, respectively), without pattern for N₂O fluxes (?3.7, 1.5, ?2.2, and ?7.6 μg N₂O m^?2 h^?1, respectively), whereas the uptake rates of CH₄ increased with stand age (6.4, ?7.9, ?10.8, and ?23.3 μg CH₄ m^?2 h^?1, respectively). For the same period, the combined contribution of CH₄ and N₂O exchanges to the global warming potential (GWP) calculated from net ecosystem exchange of CO₂ and aggregated soil exchanges of CH₄ and N₂O was on average 4%, <1%, <1%, and 2% for the 4, 17, 32, 67 years old stand, respectively. Soil CO₂ fluxes correlated positively with soil temperature but had no relationship with soil moisture. We found no control of soil temperature or soil moisture on CH₄ and N₂O fluxes, but CH₄ emission was observed following summer rainfall events. LFH layer removal reduced CO₂ emissions by 43%, increased CH₄ uptake during dry and warm soil conditions by more than twofold, but did not affect N₂O flux. We suggest that significant alternating sink and source potentials for both CH₄ and N₂O may occur in N‐ and soil water‐limited forest ecosystems, which constitute a large portion of forest cover in temperate areas.     

Methane emissions from wetlands and their relationship with vascular plants: an Arctic example

This paper investigates the relationship between vascular plant production and CH₄ emissions from an arctic wet tundra ecosystem in north‐east Greenland. Light intensity was manipulated by shading during three consecutive growing seasons (1998–2000). The shading treatment resulted in lower carbon cycling in the ecosystem as mean seasonal net ecosystem exchange (NEE) decreased from ?336 to ?196 mg CO₂ m^?2 h^?1 and from ?476 to ?212 mg CO₂ m^?2 h^?1 in 1999 and 2000, respectively, and total ecosystem respiration decreased from 125 to 94 mg CO₂ m^?2 h^?1 in 1999 and from 409 to 306 mg CO₂ m^?2 h^?1 in 2000. Seasonal mean CH₄ emissions in controls and shaded plots were, respectively, 6.5 and 4.5 mg CH₄ m^?2 h^?1 in 1999 and 8.3 and 6.2 mg CH₄ m^?2 h^?1 in 2000. We found that CH₄ emission was sensitive to NEE and carbon turnover, and it is reasonable to assume that the correlation was due to a combined effect of vegetative CH₄ transport and substrate quality coupled to vascular plant production. Total above‐ground biomass was correlated to mean seasonal CH₄ emission, but separation into species showed that plant‐mediated CH₄ transport was highly species dependent. Potential CH₄ production peaked at the same depth as maximum root density (5–15 cm) and treatment differences further suggest that substrate quality was negatively affected by decreased NEE in the shaded plots. The concentration of dissolved CH₄ decreased in the control plots as the growing season progressed while it was relatively stable in the shaded plots. This suggests that a progressively better developed root system in the controls increased the capacity to transport CH₄ from the soil to the atmosphere. In conclusion, vascular plant photosynthetic rate and subsequent allocation of recently fixed carbon to below‐ground structures seemed to influence both vegetative CH₄ transport and substrate quality.     

Recovery of Methanogenesis Following Summer Drought in Soils from Two Cool Temperate Peatlands,New York State,USA

Following a summer drought, intact cores of peat soil from two cool temperate peatlands (a rain-fed bog and a groundwater-fed swamp) were exposed experimentally to three different water table levels. The goal was to examine recovery of anaerobic methanogenesis and to evaluate peat soil decomposition to methane (CH₄), carbon dioxide (CO₂), and dissolved organic carbon (DOC) upon rewetting. Methane emission from soils to the atmosphere was greatest (mean = 80 μmol m^?2 s^?1) when the entire peat core was rewetted quickly; emission was negligible at low water level and when peat cores were rewetted gradually. Rates of CO₂ emission (mean = 1.0 μmol m^?2 s^?1) were relatively insensitive to water level. Concentrations of CH₄ in soil air spaces suggest that onset of methanogenesis induces, but later represses, aerobic oxidation of CH₄ above the water table. Concentrations of CO₂ suggest production at the soil surface of swamp peat versus at greater depths in bog peat. Portions of peat soil incubated in vitro without oxygen (O₂) exhibited a lag before the onset of methanogenesis, and the lag time was less in peat from the cores rewetted quickly. The inhibition of methanogenesis by the selective inhibitor 2-bromoethanesulfonic acid (BES) decreased CO₂ production by 20 to 30% but resulted in an increase in concentrations of DOC by 2 to 5 times. The results show that methanogens in peat soils tolerate moderate drought, and recovery varies among different peat types. In peat soils, the inhibition of methanogenesis might enhance DOC availability.     

长白山亚高山针叶林沼泽湿地碳源/汇沿水分环境梯度变化规律

高纬度和高海拔区为气候变化敏感区,该区域湿地碳循环与气候反馈关系倍受关注。为探究在全球变暖背景下高海拔区沼泽湿地碳源/汇功能是否发生了转化,以长白山高海拔区沿水分环境梯度分布的5种沼泽类型(草丛沼泽-C、灌丛沼泽-G、落叶松泥炭藓沼泽-LN、落叶松藓类沼泽-LX、落叶松苔草沼泽-LT)为对象,采用静态箱-气相色谱法和相对生长方程法,同步测定各沼泽类型全年尺度上的土壤异养呼吸碳排放量(CO₂和CH₄)、植被年净固碳量及相关环境因子(温度、水位和土壤有机碳等),并依据生态系统净碳收支平衡,量化各沼泽类型的碳源/汇作用,揭示其沿水分环境梯度变化规律及形成机制。结果表明：(1)5种沼泽类型土壤CO₂年均通量((97.68±8.64)—(291.01±18.31)mg m^-2 h^-1)沿水分环境梯度呈阶梯式递增规律性(环境梯度上部生境地段的落叶松苔草沼泽和落叶松藓类沼泽最高,中部生境地段的落叶松泥炭藓沼泽和灌丛沼泽居中,草丛沼泽最低);(2)CH₄年均通量((-0....     

Diurnal and seasonal variation in methane emissions in a northern Canadian peatland measured by eddy covariance

Eddy covariance measurements of methane (CH₄) net flux were made in a boreal fen, typical of the most abundant peatlands in western Canada during May–September 2007. The objectives of this study were to determine: (i) the magnitude of diurnal and seasonal variation in CH₄ net flux, (ii) the relationship between the temporally varying flux rates and associated changes in controlling biotic and abiotic factors, and (iii) the contribution of CH₄ emission to the ecosystem growing season carbon budget. There was significant diurnal variation in CH₄ emission during the peak of the growing season that was strongly correlated with associated changes in solar radiation, latent heat flux, air temperature and ecosystem conductance to water vapor. During days 181–215, nighttime average CH₄ efflux was only 47% of the average midday values. The peak value for daily average CH₄ emission rate was approximately 80 nmol m^?2 s^?1 (4.6 mg CH₄ m^?2 h^?1), and seasonal variation in CH₄ flux was strongly correlated with changes in soil temperature. Integrated over the entire measurement period [days 144–269 (late May–late September)], the total CH₄ emission was 3.2 g CH₄ m^?2, which was quite low relative to other wetland ecosystems and to the simultaneous high rate of ecosystem net CO₂ sequestration that was measured (18.1 mol CO₂ m^?2 or 217 g C m^?2). We estimate that the negative radiative forcing (cooling) associated with net carbon storage over the life of the peatland (approximately 2200 years) was at least twice the value of positive radiative forcing (warming) caused by net CH₄ emission over the last 50 years.     

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.     

Modelling carbon balances of coastal arctic tundra under changing climate

Rising air temperatures are believed to be hastening heterotrophic respiration (R_h) in arctic tundra ecosystems, which could lead to substantial losses of soil carbon (C). In order to improve confidence in predicting the likelihood of such loss, the comprehensive ecosystem model ecosys was first tested with carbon dioxide (CO₂) fluxes measured over a tundra soil in a growth chamber under various temperatures and soil‐water contents (θ). The model was then tested with CO₂ and energy fluxes measured over a coastal arctic tundra near Barrow, Alaska, under a range of weather conditions during 1998–1999. A rise in growth chamber temperature from 7 to 15 °C caused large, but commensurate, rises in respiration and CO₂ fixation, and so no significant effect on net CO₂ exchange was modelled or measured. An increase in growth chamber θ from field capacity to saturation caused substantial reductions in respiration but not in CO₂ fixation, and so an increase in net CO₂ exchange was modelled and measured. Long daylengths over the coastal tundra at Barrow caused an almost continuous C sink to be modelled and measured during most of July (2–4 g C m^?2 d^?1), but shortening daylengths and declining air temperatures caused a C source to be modelled and measured by early September (～1 g C m^?2 d^?1). At an annual time scale, the coastal tundra was modelled to be a small C sink (4 g C m^?2 y^?1) during 1998 when average air temperatures were 4 °C above normal, and a larger C sink (16 g C m^?2 y^?1) during 1999 when air temperatures were close to long‐term normals. During 100 years under rising atmospheric CO₂ concentration (C_a), air temperature and precipitation driven by the IS92a emissions scenario, modelled R_h rose commensurately with net primary productivity (NPP) under both current and elevated rates of atmospheric nitrogen (N) deposition, so that changes in soil C remained small. However, methane (CH₄) emissions were predicted to rise substantially in coastal tundra with IS92a‐driven climate change (from ～20 to ～40 g C m^?2 y^?1), causing a substantial increase in the emission of CO₂ equivalents. If the rate of temperature increase hypothesized in the IS92a emissions scenario had been raised by 50%, substantial losses of soil C (～1 kg C m^?2) would have been modelled after 100 years, including additional emissions of CH₄.     

Spatial and temporal dynamics of diffusive methane emissions in the Okavango Delta,northern Botswana,Africa

Global warming is associated with the continued increase in the atmospheric concentrations of greenhouse gases; carbon dioxide, methane (CH₄) and nitrous oxide. Wetlands constitute the largest single natural source of atmospheric CH₄ in the world contributing between 100 and 231 Tg year^?1 to the total budget of 503–610 Tg year^?1, approximately 60 % of which is emitted from tropical wetlands. We conducted diffusive CH₄ emission measurements using static chambers in river channels, floodplains and lagoons in permanent and seasonal swamps in the Okavango Delta, Botswana. Diffusive CH₄ emission rates varied between 0.24 and 293 mg CH₄ m^?2 h^?1, with a mean (±SE) emission of 23.2 ± 2.2 mg CH₄ m^?2 h^?1 or 558 ± 53 mg CH₄ m^?2 day^?1. These emission rates lie within the range reported for other tropical wetlands. The emission rates were significantly higher (P < 0.007) in permanent than in seasonal swamps. River channels exhibited the highest average fluxes at 31.3 ± 5.4 mg CH₄ m^?2 h^?1 than in floodplains (20.4 ± 2.5 mg CH₄ m^?2 h^?1) and lagoons (16.9 ± 2.6 mg CH₄ m^?2 h^?1). Diffusive CH₄ emissions in the Delta were probably regulated by temperature since emissions were highest (20–300 mg CH₄ m^?2 h^?1) and lowest (0.2–3.0 mg m^?2 h^?1) during the warmer-rainy and cooler winter seasons, respectively. Surface water temperatures between December 2010 and January 2012 varied from 15.3 °C in winter to 33 °C in summer. Assuming mean inundation of 9,000 km², the Delta’s annual diffusive emission was estimated at 1.8 ± 0.2 Tg, accounting for 2.8 ± 0.3 % of the total CH₄ emission from global tropical wetlands.     

Soil–atmosphere exchange of greenhouse gases in a Eucalyptus marginata woodland, a clover-grass pasture, and Pinus radiata and Eucalyptus globulus plantations

Soils provide the largest terrestrial carbon store, the largest atmospheric CO₂ source, the largest terrestrial N₂O source and the largest terrestrial CH₄ sink, as mediated through root and soil microbial processes. A change in land use or management can alter these soil processes such that net greenhouse gas exchange may increase or decrease. We measured soil–atmosphere exchange of CO₂, N₂O and CH₄ in four adjacent land‐use systems (native eucalypt woodland, clover‐grass pasture, Pinus radiata and Eucalyptus globulus plantation) for short, but continuous, periods between October 2005 and June 2006 using an automated trace gas measurement system near Albany in southwest Western Australia. Mean N₂O emission in the pasture was 26.6 μg N m⁻² h⁻¹, significantly greater than in the natural and managed forests (< 2.0 μg N m⁻² h⁻¹). N₂O emission from pasture soil increased after rainfall events (up to 100 μg N m⁻² h⁻¹) and as soil water content increased into winter, whereas no soil water response was detected in the forest systems. Gross nitrification through ¹⁵N isotope dilution in all land‐use systems was small at water holding capacity < 30%, and under optimum soil water conditions gross nitrification ranged between < 0.1 and 1.0 mg N kg⁻¹ h⁻¹, being least in the native woodland/eucalypt plantation < pine plantation < pasture. Forest soils were a constant CH₄ sink, up to −20 μg C m⁻² h⁻¹ in the native woodland. Pasture soil was an occasional CH₄ source, but weak CH₄ sink overall (−3 μg C m⁻² h⁻¹). There were no strong correlations (R < 0.4) between CH₄ flux and soil moisture or temperature. Soil CO₂ emissions (35–55 mg C m⁻² h⁻¹) correlated with soil water content (R < 0.5) in all but the E. globulus plantation. Soil N₂O emissions from improved pastures can be considerable and comparable with intensively managed, irrigated and fertilised dairy pastures. In all land uses, soil N₂O emissions exceeded soil CH₄ uptake on a carbon dioxide equivalent basis. Overall, afforestation of improved pastures (i) decreases soil N₂O emissions and (ii) increases soil CH₄ uptake.     

Emission of N2O, N2, CH4, and CO2 from constructed wetlands for wastewater treatment and from riparian buffer zones

We measured nitrous oxide (N₂O), dinitrogen (N₂), methane (CH₄), and carbon dioxide (CO₂) fluxes in horizontal and vertical flow constructed wetlands (CW) and in a riparian alder stand in southern Estonia using the closed chamber method in the period from October 2001 to November 2003. The replicates’ average values of N₂O, N₂, CH₄ and CO₂ fluxes from the riparian gray alder stand varied from −0.4 to 58 μg N₂O-N m⁻² h⁻¹, 0.02–17.4 mg N₂-N m⁻² h⁻¹, 0.1–265 μg CH₄-C m⁻² h⁻¹ and 55–61 mg CO₂-C m⁻² h⁻¹, respectively. In horizontal subsurface flow (HSSF) beds of CWs, the average N₂ emission varied from 0.17 to 130 and from 0.33 to 119 mg N₂-N m⁻² h⁻¹ in the vertical subsurface flow (VSSF) beds. The average N₂O-N emission from the microsites above the inflow pipes of the HSSF CWs was 6.4–31 μg N₂O-N m⁻² h⁻¹, whereas the outflow microsites emitted 2.4–8 μg N₂O-N m⁻² h⁻¹. In VSSF beds, the same value was 35.6–44.7 μg N₂O-N m⁻² h⁻¹. The average CH₄ emission from the inflow and outflow microsites in the HSSF CWs differed significantly, ranging from 640 to 9715 and from 30 to 770 μg CH₄-C m⁻² h⁻¹, respectively. The average CO₂ emission was somewhat higher in VSSF beds (140–291 mg CO₂-C m⁻² h⁻¹) and at the inflow microsites of HSSF beds (61–140 mg CO₂-C m⁻² h⁻¹). The global warming potential (GWP) from N₂O and CH₄ was comparatively high in both types of CWs (4.8 ± 9.8 and 6.8 ± 16.2 t CO₂ eq ha⁻¹ a⁻¹ in the HSSF CW 6.5 ± 13.0 and 5.3 ± 24.7 t CO₂ eq ha⁻¹ a⁻¹ in the hybrid CW, respectively). The GWP of the riparian alder forest from both N₂O and CH₄ was relatively low (0.4 ± 1.0 and 0.1 ± 0.30 t CO₂ eq ha⁻¹ a⁻¹, respectively), whereas the CO₂-C flux was remarkable (3.5 ± 3.7 t ha⁻¹ a⁻¹). The global influence of CWs is not significant. Even if all global domestic wastewater were treated by wetlands, their share of the trace gas emission budget would be less than 1%.     

Microbial and Environmental Controls of Methane Fluxes Along a Soil Moisture Gradient in a Pacific Coastal Temperate Rainforest

Most studies of greenhouse gas fluxes from forest soils in the coastal rainforest have considered carbon dioxide (CO₂), whereas methane (CH₄) has not received the same attention. Soil hydrology is a key driver of CH₄ dynamics in ecosystems, but the impact on the function and distribution of the underlying microbial communities involved in CH₄ cycling and the resultant net CH₄ exchange is not well understood at this scale. We studied the growing season variations of in situ CH₄ fluxes, microbial gene abundances of methanotrophs (CH₄ oxidizers) and methanogens (CH₄ producers), soil hydrology, and nutrient availability in three typical forest types across a soil moisture gradient. CH₄ displayed a spatial variability changing from a net uptake in the upland soils (3.9–46 µmol CH₄ m^?2 h^?1) to a net emission in the wetter soils (0–90 μmol CH₄ m^?2 h^?1). Seasonal variations of CH₄ fluxes were related to soil hydrology in both upland and wet soils. Thus, in the upland soils, uptake rates increased with the decreasing soil moisture, whereas CH₄ emission was inversely related to the water table depth in the wet soils. Spatial variability of CH₄ exchange was related to the abundance of genes involved in CH₄ oxidation and production, but there was no indication of a temporal link between microbial groups and CH₄ exchange. Our data show that the abundances of genes involved in CH₄ oxidation and production are strongly influenced by soil moisture and each other and grouped by the upland–wetland classification but not forest type.     

Soil N and C trace gas fluxes and microbial soil N turnover in a sessile oak (Quercus petraea (Matt.) Liebl.) forest in Hungary

During two intensive field campaigns in summer and autumn 2004 nitrogen (N₂O, NO/NO₂) and carbon (CO₂, CH₄) trace gas exchange between soil and the atmosphere was measured in a sessile oak (Quercus petraea (Matt.) Liebl.) forest in Hungary. The climate can be described as continental temperate. Fluxes were measured with a fully automatic measuring system allowing for high temporal resolution. Mean N₂O emission rates were 1.5 μg N m⁻² h⁻¹ in summer and 3.4 μg N m⁻² h⁻¹ in autumn, respectively. Also mean NO emission rates were higher in autumn (8.4 μg N m⁻² h⁻¹) as compared to summer (6.0 μg N m⁻² h⁻¹). However, as NO₂ deposition rates continuously exceeded NO emission rates (−9.7 μg N m⁻² h⁻¹ in summer and −18.3 μg N m⁻² h⁻¹ in autumn), the forest soil always acted as a net NO _x sink. The mean value of CO₂ fluxes showed only little seasonal differences between summer (81.1 mg C m⁻² h⁻¹) and autumn (74.2 mg C m⁻² h⁻¹) measurements, likewise CH₄uptake (summer: −52.6 μg C m⁻² h⁻¹; autumn: −56.5 μg C m⁻² h⁻¹). In addition, the microbial soil processes net/gross N mineralization, net/gross nitrification and heterotrophic soil respiration as well as inorganic soil nitrogen concentrations and N₂O/CH₄ soil air concentrations in different soil depths were determined. The respiratory quotient (ΔCO_{2 resp} ΔO_{2 resp}⁻¹) for the uppermost mineral soil, which is needed for the calculation of gross nitrification via the Barometric Process Separation (BaPS) technique, was 0.8978 ± 0.008. The mean value of gross nitrification rates showed only little seasonal differences between summer (0.99 μg N kg⁻¹ SDW d⁻¹) and autumn measurements (0.89 μg N kg⁻¹ SDW d⁻¹). Gross rates of N mineralization were highest in the organic layer (20.1–137.9 μg N kg⁻¹ SDW d⁻¹) and significantly lower in the uppermost mineral layer (1.3–2.9 μg N kg⁻¹ SDW d⁻¹). Only for the organic layer seasonality in gross N mineralization rates could be demonstrated, with highest mean values in autumn, most likely caused by fresh litter decomposition. Gross mineralization rates of the organic layer were positively correlated with N₂O emissions and negatively correlated with CH₄ uptake, whereas soil CO₂ emissions were positively correlated with heterotrophic respiration in the uppermost mineral soil layer. The most important abiotic factor influencing C and N trace gas fluxes was soil moisture, while the influence of soil temperature on trace gas exchange rates was high only in autumn.     

Transitional slopes act as hotspots of both soil CO<Subscript>2</Subscript> emission and CH<Subscript>4</Subscript> uptake in a temperate forest landscape

Forest soils are an important component of CO₂ and CH₄ fluxes at the global scale, but the magnitude of these fluxes varies greatly in space and time within a landscape. Understanding the spatial and temporal distributions of these fluxes across complex landscapes remains a major challenge for researchers and land managers alike. We investigated the spatiotemporal variability of soil-atmosphere CO₂ and CH₄ fluxes and the relationships of these fluxes to chemical and physical soil properties distributed across a topographically-heterogeneous landscape. Soil CO₂ and CH₄ fluxes were measured along with soil temperature, moisture, bulk density, texture, carbon, sorption capacity, and dissolved organic matter quality over 2 years along hillslope transects spanning valley bottom, transition zone, and upland landscape positions in a temperate forest watershed. Transition zone soil CO₂ efflux was 54–160% higher than low-lying valley bottoms, and 15–54% higher than uplands. Net seasonal CH₄ uptake was 58–150% higher in transition zone soils than in uplands, while valley bottoms were occasionally large net sources (up to 19 nmol CH₄ m^?2 s^?1). Soil CO₂ efflux and net CH₄ uptake were both positively associated with seasonal temperature, and were highest in soils with relatively high carbon and clay content, and relatively low bulk density, moisture, and sorption capacity. We concluded that: (1) transition zone soils act as landscape hotspots for net CH₄ uptake in addition to CO₂ efflux, and (2) that this spatial distribution is more consistent across seasons for net CH₄ uptake than for CO₂ efflux.     

The response of soil CO2 flux to changes in atmospheric CO2, nitrogen supply and plant diversity

We measured soil CO₂ flux over 19 sampling periods that spanned two growing seasons in a grassland Free Air Carbon dioxide Enrichment (FACE) experiment that factorially manipulated three major anthropogenic global changes: atmospheric carbon dioxide (CO₂) concentration, nitrogen (N) supply, and plant species richness. On average, over two growing seasons, elevated atmospheric CO₂ and N fertilization increased soil CO₂ flux by 0.57 µmol m^?2 s^?1 (13% increase) and 0.37 µmol m^?2 s^?1 (8% increase) above average control soil CO₂ flux, respectively. Decreases in planted diversity from 16 to 9, 4 and 1 species decreased soil CO₂ flux by 0.23, 0.41 and 1.09 µmol m^?2 s^?1 (5%, 8% and 21% decreases), respectively. There were no statistically significant pairwise interactions among the three treatments. During 19 sampling periods that spanned two growing seasons, elevated atmospheric CO₂ increased soil CO₂ flux most when soil moisture was low and soils were warm. Effects on soil CO₂ flux due to fertilization with N and decreases in diversity were greatest at the times of the year when soils were warm, although there were no significant correlations between these effects and soil moisture. Of the treatments, only the N and diversity treatments were correlated over time; neither were correlated with the CO₂ effect. Models of soil CO₂ flux will need to incorporate ecosystem CO₂ and N availability, as well as ecosystem plant diversity, and incorporate different environmental factors when determining the magnitude of the CO₂, N and diversity effects on soil CO₂ flux.     

Methane and carbon dioxide dynamics within four vernal pools in Maine,USA

Vernal pools are small, seasonal wetlands that are a common landscape feature contributing to biodiversity in northeastern North American forests. Basic information about their biogeochemical functions, such as carbon cycling, is limited. Concentrations of dissolved methane (CH₄) and carbon dioxide (CO₂) and other water chemistry parameters were monitored weekly at the bottom and surface of four vernal pools in central and eastern Maine, USA, from April to August 2016. The vernal pools were supersaturated with respect to CH₄ and CO₂ at all sampling dates and locations. Concentrations of dissolved CH₄ and CO₂ ranged from 0.4 to 210 μmol L^?1 and 72–2300 μmol L^?1, respectively. Diffusive fluxes of CH₄ and CO₂ into the atmosphere ranged from 0.2 to 73 mmol m^?2 d^?1, and 30–590 mmol m^?2 d^?1, respectively. During the study period, the four vernal pools emitted 0.1–5.8 kg C m^?2 and 9.6–120 kg C m^?2 as CH₄ and CO₂, respectively. The production fluxes (production rates normalized to surface area) of CH₄ and CO₂ ranged from ? 0.02 to 0.66 and 0.40–4.6 g C m^?2 d^?1, respectively, and increased significantly over the season. Methane concentrations were best predicted by alkalinity, ortho-phosphate and depth, while CO₂ concentrations were best predicted with only alkalinity. Alkalinity as a predictor variable highlights the importance of anaerobic respiration in production of both gases. Our study pools had large concentrations and effluxes of CH₄ and CO₂ compared to permanently inundated wetlands, indicating vernal pools are metabolically active sites and may be important contributors to the global carbon budget.     

Dynamics of gaseous nitrogen and carbon fluxes in riparian alder forests

We studied greenhouse gas (GHG) fluxes in two differently loaded riparian Alnus incana-dominated forests in agricultural landscapes of southern Estonia: a 33-year-old stand in Porijõgi, in which the uphill agricultural activities had been abandoned since the middle of the 1990s, and a 50-year-old stand in Viiratsi, which still receives polluted lateral flow from uphill fields fertilized with pig slurry. In Porijõgi, closed-chamber based sampling lasted from October 2001 to October 2009, whereas in Viiratsi the sampling period was from November 2003 to October 2009. Both temporal and spatial variations in all GHG gas fluxes were remarkable. Local differences in GHG fluxes between micro-sites (“Edge”, “Dry” and “Wet” in Porijõgi, and “Wet”, “Slope” and “Dry” in Viiratsi) were sometimes greater than those between sites. Median values of GHG fluxes from both sites over the whole study period and all microsites did not differ significantly, being 45 and 42 mg CO₂-C m⁻² h⁻¹, 8 and 0.5 μg CH₄-C m⁻² h⁻¹, 1.0 and 2.1 mg N₂-N m⁻² h⁻¹, and 5 and 9 μg N₂O-N m⁻² h⁻¹, in Porijõgi and Viiratsi, respectively. The N₂:N₂O ratio in Viiratsi (40-1200) was lower than in Porijõgi (10-7600). The median values-based estimation of the Global Warming Potential of CH₄ and N₂O was 19 and 185 kg CO₂ equivalents (eq) ha⁻¹ yr⁻¹ in Porijõgi and −14 and 336 kg CO₂ eq ha⁻¹ yr⁻¹ in Viiratsi, respectively. A significant Spearman rank correlation was found between the mean monthly air temperature and CO₂, CH₄ and N₂ fluxes in Porijõgi, and N₂O flux in Viiratsi, and between the monthly precipitation and CH₄ fluxes in both study sites. Higher groundwater level significantly increases CH₄ emission and decreases CO₂ and N₂O emission, whereas higher soil temperature significantly increases N₂O, CH₄ and N₂ emission values. In Porijõgi, GHG emissions did not display any discernable trend, whereas in Viiratsi a significant increase in CO₂, N₂, and N₂O emissions has been found. This may be a result of the age of the grey alder stand, but may also be caused by the long-term nutrient load of this riparian alder stand, which indicates a need for the management of similar heavily loaded riparian alder stands.     

Influence of weather variables on methane and carbon dioxide flux from a shallow pond

Freshwaters are important sources of the greenhouse gases methane (CH₄) and carbon dioxide (CO₂) to the atmosphere. Knowledge about temporal variability in these fluxes is very limited, yet critical for proper study design and evaluating flux data. Further, to understand the reasons for the variability and allow predictive modeling, the temporal variability has to be related to relevant environmental variables. Here we analyzed the effect of weather variables on CH₄ and CO₂ flux from a small shallow pond during a period of 4 months. Mean CH₄ flux and surface water CH₄ concentration were 8.0 [3.3–15.1] ± 3.1 mmol m^?2 day^?1 (mean [range] ± 1 SD) and 1.3 [0.3–3.5] ± 0.9 µM respectively. Mean CO₂ flux was 1.1 [?9.8 to 16.0] ± 6.9 mmol m^?2 day^?1. Substantial diel changes in CO₂ flux and surface water CH₄ concentration were observed during detailed measurements over a 24 h cycle. Thus diel patterns need to be accounted for in future measurements. Significant positive correlations of CH₄ emissions with temperature were found and could include both direct temperature effects as well as indirect effects (e.g. related to the growth season and macrophyte primary productivity providing organic substrates). CO₂ flux on the other hand was negatively correlated to temperature and solar radiation, presumably because CO₂ consumption by plants was higher relative to CO₂ production by respiration during warm sunny days. Interestingly, CH₄ fluxes were comparable to ponds with similar morphometry and macrophyte abundance in the tropics. We therefore hypothesize that CH₄ and CO₂ summer emissions from ponds could be more related to the morphometry and dominating primary producers rather than latitude per se. Data indicate that CH₄ emissions, given the system characteristic frameworks, is positively affected by increased temperatures or prolonged growth seasons.     

冬季水分管理和水稻覆膜栽培对川中丘陵地区冬水田CH4排放的影响

采用静态箱-气相色谱法观测冬季水分管理和水稻覆膜栽培对川中丘陵地区冬水田全年的CH_4排放通量。试验设置持续淹水(CF)、冬季直接落干+稻季淹水(TF)与冬季覆膜落干+稻季覆膜(PM)3个处理。结果表明,冬季休闲期,CF、TF和PM处理CH_4排放分别为16.1、1.4 g/m~2和2.7 g/m~2;水稻生长期,CF、TF和PM处理CH_4排放分别为57.7、27.7 g/m~2和13.5 g/m~2。相较于CF处理,TF与PM处理分别减少其全年CH_4排放60.6%和78.0%。TF与PM处理水稻生长期CH_4排放峰值分别较CF处理低33.0%和56.1%。休闲期,TF、PM处理厢面与厢沟区域CH_4排放与土壤温度显著正相关(P0.05),与土壤氧化还原电位(土壤Eh)显著负相关(P0.05),而CF处理CH_4排放仅与土壤温度显著正相关(P0.05)。水稻生长期,CF处理CH_4排放与土壤温度显著正相关(P0.05),与土壤Eh显著负相关(P0.05),TF处理CH_4排放仅与土壤Eh显著负相关(P0.05),PM处理厢沟CH_4排放与土壤Eh显著正相关(P0.05)。各处理水稻生长期土壤可溶性有机碳含量(DOC)与微生物生物量碳含量(MBC)显著高于休闲期(P0.05)。研究结果为进一步研究冬水田全年CH_4排放规律及寻求有效的减排措施提供数据支撑和科学依据。     

Seasonal and spatial variations of methane emissions from coastal marshes in the northern Yellow River estuary, China

Aims and methods

To evaluate the seasonal and spatial variations of methane (CH₄) emissions and understand the controlling factors, we measured CH₄ fluxes and their environmental variables for the first time by a static chamber technique in high Suaeda salsa marsh (HSM), middle S. salsa marsh (MSM), low S. salsa marsh (LSM) and bare flat (BF) in the northern Yellow River estuary throughout a year.

Results

CH₄ emissions from coastal marsh varied throughout different times of the day and significant differences were observed in some sampling periods (p?<?0.05). Over all sampling periods, CH₄ fluxes averaged between ?0.392 mgCH₄ m^?2?h^?1 and 0.495 mgCH₄ m^?2?h^?1, and emissions occurred during spring (0.008 mgCH₄ m^?2?h^?1) and autumn (0.068 mgCH₄ m^?2?h^?1) while sinks were observed during summer (?0.110 mgCH₄ m^?2?h^?1) and winter (?0.009 mgCH₄ m^?2?h^?1). CH₄ fluxes from the four marshes were not significantly different (p?>?0.05), and emissions occurred in LSM (0.026 mgCH₄ m^?2?h^?1) and BF (0.055 mgCH₄ m^?2?h^?1) while sinks were observed in HSM (?0.035 mgCH₄ m^?2?h^?1) and MSM (?0.022 mgCH₄ m^?2?h^?1). The annual average CH₄ flux from the intertidal zone was 0.002 mgCH₄ m^?2?h^?1, indicating that coastal marsh acted as a weak CH₄ source. Temporal variations of CH₄ emission were related to the interactions of abiotic factors (temperatures, soil moisture and salinity) and the variations of limited C and mineral N in sediments, while spatial variations were mainly affected by the vegetation composition at spatial scale.

Conclusions

This study observed a large spatial variation of CH₄ fluxes across the coastal marsh of the Yellow River estuary (CV?=?7856.25 %), suggesting that the need to increase the spatial replicates at fine scales before the regional CH₄ budget was evaluated precisely. With increasing exogenous nitrogen loading to the Yellow River estuary, the magnitude of CH₄ emission might be enhanced, which should also be paid more attentions as the annual CH₄ inventory was assessed accurately.     

不同恢复方式下大兴安岭重度火烧迹地林地土壤温室气体通量

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