Long‐term impacts of manure amendments on carbon and greenhouse gas dynamics of rangelands

Livestock manure is applied to rangelands as an organic fertilizer to stimulate forage production, but the long‐term impacts of this practice on soil carbon (C) and greenhouse gas (GHG) dynamics are poorly known. We collected soil samples from manured and nonmanured fields on commercial dairies and found that manure amendments increased soil C stocks by 19.0 ± 7.3 Mg C ha^?1 and N stocks by 1.94 ± 0.63 Mg N ha^?1 compared to nonmanured fields (0–20 cm depth). Long‐term historical (1700–present) and future (present–2100) impacts of management on soil C and N dynamics, net primary productivity (NPP), and GHG emissions were modeled with DayCent. Modeled total soil C and N stocks increased with the onset of dairying. Nitrous oxide (N₂O) emissions also increased by ~2 kg N₂O‐N ha^?1 yr^?1. These emissions were proportional to total N additions and offset 75–100% of soil C sequestration. All fields were small net methane (CH₄) sinks, averaging ?4.7 ± 1.2 kg CH₄‐C ha^?1 yr^?1. Overall, manured fields were net GHG sinks between 1954 and 2011 (?0.74 ± 0.73 Mg CO₂ e ha^?1 yr^?1, CO₂e are carbon dioxide equivalents), whereas nonmanured fields varied around zero. Future soil C pools stabilized 40–60 years faster in manured fields than nonmanured fields, at which point manured fields were significantly larger sources than nonmanured fields (1.45 ± 0.52 Mg CO₂e ha^?1 yr^?1 and 0.51 ± 0.60 Mg CO₂e ha^?1 yr^?1, respectively). Modeling also revealed a large background loss of soil C from the passive soil pool associated with the shift from perennial to annual grasses, equivalent to 29.4 ± 1.47 Tg CO₂e in California between 1820 and 2011. Manure applications increased NPP and soil C storage, but plant community changes and GHG emissions decreased, and eventually eliminated, the net climate benefit of this practice.     

Effects of seasonality,transport pathway,and spatial structure on greenhouse gas fluxes in a restored wetland

Wetlands can influence global climate via greenhouse gas (GHG) exchange of carbon dioxide (CO₂), methane (CH₄), and nitrous oxide (N₂O). Few studies have quantified the full GHG budget of wetlands due to the high spatial and temporal variability of fluxes. We report annual open‐water diffusion and ebullition fluxes of CO₂, CH₄, and N₂O from a restored emergent marsh ecosystem. We combined these data with concurrent eddy‐covariance measurements of whole‐ecosystem CO₂ and CH₄ exchange to estimate GHG fluxes and associated radiative forcing effects for the whole wetland, and separately for open‐water and vegetated cover types. Annual open‐water CO₂, CH₄, and N₂O emissions were 915 ± 95 g C‐CO₂ m^?2 yr^?1, 2.9 ± 0.5 g C‐CH₄ m^?2 yr^?1, and 62 ± 17 mg N‐N₂O m^?2 yr^?1, respectively. Diffusion dominated open‐water GHG transport, accounting for >99% of CO₂ and N₂O emissions, and ~71% of CH₄ emissions. Seasonality was minor for CO₂ emissions, whereas CH₄ and N₂O fluxes displayed strong and asynchronous seasonal dynamics. Notably, the overall radiative forcing of open‐water fluxes (3.5 ± 0.3 kg CO₂‐eq m^?2 yr^?1) exceeded that of vegetated zones (1.4 ± 0.4 kg CO₂‐eq m^?2 yr^?1) due to high ecosystem respiration. After scaling results to the entire wetland using object‐based cover classification of remote sensing imagery, net uptake of CO₂ (?1.4 ± 0.6 kt CO₂‐eq yr^?1) did not offset CH₄ emission (3.7 ± 0.03 kt CO₂‐eq yr^?1), producing an overall positive radiative forcing effect of 2.4 ± 0.3 kt CO₂‐eq yr^?1. These results demonstrate clear effects of seasonality, spatial structure, and transport pathway on the magnitude and composition of wetland GHG emissions, and the efficacy of multiscale flux measurement to overcome challenges of wetland heterogeneity.     

Land‐use change to bioenergy: grassland to short rotation coppice willow has an improved carbon balance

The effect of a transition from grassland to second‐generation (2G) bioenergy on soil carbon and greenhouse gas (GHG) balance is uncertain, with limited empirical data on which to validate landscape‐scale models, sustainability criteria and energy policies. Here, we quantified soil carbon, soil GHG emissions and whole ecosystem carbon balance for short rotation coppice (SRC) bioenergy willow and a paired grassland site, both planted at commercial scale. We quantified the carbon balance for a 2‐year period and captured the effects of a commercial harvest in the SRC willow at the end of the first cycle. Soil fluxes of nitrous oxide (N₂O) and methane (CH₄) did not contribute significantly to the GHG balance of these land uses. Soil respiration was lower in SRC willow (912 ± 42 g C m^?2 yr^?1) than in grassland (1522 ± 39 g C m^?2 yr^?1). Net ecosystem exchange (NEE) reflected this with the grassland a net source of carbon with mean NEE of 119 ± 10 g C m^?2 yr^?1 and SRC willow a net sink, ?620 ± 18 g C m^?2 yr^?1. When carbon removed from the ecosystem in harvested products was considered (Net Biome Productivity), SRC willow remained a net sink (221 ± 66 g C m^?2 yr^?1). Despite the SRC willow site being a net sink for carbon, soil carbon stocks (0–30 cm) were higher under the grassland. There was a larger NEE and increase in ecosystem respiration in the SRC willow after harvest; however, the site still remained a carbon sink. Our results indicate that once established, significant carbon savings are likely in SRC willow compared with the minimally managed grassland at this site. Although these observed impacts may be site and management dependent, they provide evidence that land‐use transition to 2G bioenergy has potential to provide a significant improvement on the ecosystem service of climate regulation relative to grassland systems.     

Effect of catchment characteristics on aquatic carbon export from a boreal catchment and its importance in regional carbon cycling

Inland waters transport and emit into the atmosphere large amounts of carbon (C), which originates from terrestrial ecosystems. The effect of land cover and land‐use practises on C export from terrestrial ecosystems to inland waters is not fully understood, especially in heterogeneous landscapes under human influence. We sampled for dissolved C species in five tributaries with well‐determined subcatchments (total size 174.5 km²), as well as in various points of two of the subcatchments draining to a boreal lake in southern Finland over a full year. Our aim was to find out how land cover and land‐use affect C export from the catchments, as well as CH₄ and CO₂ concentrations of the streams, and if the origin of C in stream water can be determined from proxies for quality of dissolved organic matter (DOM). We further estimated the gas evasion from stream surfaces and the role of aquatic fluxes in regional C cycling. The export rate of C from the terrestrial system through an aquatic conduit was 19.3 g C m^?2(catchment) yr^?1, which corresponds to 19% of the estimated terrestrial net ecosystem exchange of the catchment. Most of the C load to the recipient lake consisted of dissolved organic carbon (DOC, 6.1 ± 1.0 g C m^?2 yr^?1); the share of dissolved inorganic carbon (DIC) was much smaller (1.0 ± 0.2 g C m^?2 yr^?1). CO₂ and CH₄ emissions from stream and ditch surfaces were 7.0 ± 2.4 g C m^?2 yr^?1 and 0.1 ± 0.04 g C m^?2 yr^?1, respectively, C emissions being thus equal with C load to the lake. The proportion of peatland in the catchment and the drainage density of peatland increased DOC in streams, whereas the proportion of agricultural land in the catchment decreased it. The opposite was true for DIC. Drained peatlands were an important CH₄ source for streams.     

The positive net radiative greenhouse gas forcing of increasing methane emissions from a thawing boreal forest‐wetland landscape

At the southern margin of permafrost in North America, climate change causes widespread permafrost thaw. In boreal lowlands, thawing forested permafrost peat plateaus (‘forest’) lead to expansion of permafrost‐free wetlands (‘wetland’). Expanding wetland area with saturated and warmer organic soils is expected to increase landscape methane (CH₄) emissions. Here, we quantify the thaw‐induced increase in CH₄ emissions for a boreal forest‐wetland landscape in the southern Taiga Plains, Canada, and evaluate its impact on net radiative forcing relative to potential long‐term net carbon dioxide (CO₂) exchange. Using nested wetland and landscape eddy covariance net CH₄ flux measurements in combination with flux footprint modeling, we find that landscape CH₄ emissions increase with increasing wetland‐to‐forest ratio. Landscape CH₄ emissions are most sensitive to this ratio during peak emission periods, when wetland soils are up to 10 °C warmer than forest soils. The cumulative growing season (May–October) wetland CH₄ emission of ~13 g CH₄ m^?2 is the dominating contribution to the landscape CH₄ emission of ~7 g CH₄ m^?2. In contrast, forest contributions to landscape CH₄ emissions appear to be negligible. The rapid wetland expansion of 0.26 ± 0.05% yr^?1 in this region causes an estimated growing season increase of 0.034 ± 0.007 g CH₄ m^?2 yr^?1 in landscape CH₄ emissions. A long‐term net CO₂ uptake of >200 g CO₂ m^?2 yr^?1 is required to offset the positive radiative forcing of increasing CH₄ emissions until the end of the 21st century as indicated by an atmospheric CH₄ and CO₂ concentration model. However, long‐term apparent carbon accumulation rates in similar boreal forest‐wetland landscapes and eddy covariance landscape net CO₂ flux measurements suggest a long‐term net CO₂ uptake between 49 and 157 g CO₂ m^?2 yr^?1. Thus, thaw‐induced CH₄ emission increases likely exert a positive net radiative greenhouse gas forcing through the 21st century.     

Methane and carbon dioxide emissions from inland waters in India – implications for large scale greenhouse gas balances

Inland waters were recently recognized to be important sources of methane (CH₄) and carbon dioxide (CO₂) to the atmosphere, and including inland water emissions in large scale greenhouse gas (GHG) budgets may potentially offset the estimated carbon sink in many areas. However, the lack of GHG flux measurements and well‐defined inland water areas for extrapolation, make the magnitude of the potential offset unclear. This study presents coordinated flux measurements of CH₄ and CO₂ in multiple lakes, ponds, rivers, open wells, reservoirs, springs, and canals in India. All these inland water types, representative of common aquatic ecosystems in India, emitted substantial amounts of CH₄ and a major fraction also emitted CO₂. The total CH₄ flux (including ebullition and diffusion) from all the 45 systems ranged from 0.01 to 52.1 mmol m^?2 d^?1, with a mean of 7.8 ± 12.7 (mean ± 1 SD) mmol m^?2 d^?1. The mean surface water CH₄ concentration was 3.8 ± 14.5 μm (range 0.03–92.1 μm ). The CO₂ fluxes ranged from ?28.2 to 262.4 mmol m^?2 d^?1 and the mean flux was 51.9 ± 71.1 mmol m^?2 d^?1. The mean partial pressure of CO₂ was 2927 ± 3269 μatm (range: 400–11 467 μatm). Conservative extrapolation to whole India, considering the specific area of the different water types studied, yielded average emissions of 2.1 Tg CH₄ yr^?1 and 22.0 Tg CO₂ yr^?1 from India's inland waters. When expressed as CO₂ equivalents, this amounts to 75 Tg CO₂ equivalents yr^?1 (53–98 Tg CO₂ equivalents yr^?1; ± 1 SD)_, with CH₄ contributing 71%. Hence, average inland water GHG emissions, which were not previously considered, correspond to 42% (30–55%) of the estimated land carbon sink of India. Thereby this study illustrates the importance of considering inland water GHG exchange in large scale assessments.     

Soil‐derived trace gas fluxes from different energy crops – results from a field experiment in Southwest Germany

Willow coppice, energy maize and Miscanthus were evaluated regarding their soil‐derived trace gas emission potential involving a nonfertilized and a crop‐adapted slow‐release nitrogen (N) fertilizer scheme. The N application rate was 80 kg N ha^?1 yr^?1 for the perennial crops and 240 kg N ha^?1 yr^?1 for the annual maize. A replicated field experiment was conducted with 1‐year measurements of soil fluxes of CH₄, CO₂ and N₂O in weekly intervals using static chambers. The measurements revealed a clear seasonal trend in soil CO₂ emissions, with highest emissions being found for the N‐fertilized Miscanthus plots (annual mean: 50 mg C m^?² h^?1). Significant differences between the cropping systems were found in soil N₂O emissions due to their dependency on amount and timing of N fertilization. N‐fertilized maize plots had highest N₂O emissions by far, which accumulated to 3.6 kg N₂O ha^?1 yr^?1. The contribution of CH₄ fluxes to the total soil greenhouse gas subsumption was very small compared with N₂O and CO₂. CH₄ fluxes were mostly negative indicating that the investigated soils mainly acted as weak sinks for atmospheric CH₄. To identify the system providing the best ratio of yield to soil N₂O emissions, a subsumption relative to biomass yields was calculated. N‐fertilized maize caused the highest soil N₂O emissions relative to dry matter yields. Moreover, unfertilized maize had higher relative soil N₂O emissions than unfertilized Miscanthus and willow. These results favour perennial crops for bioenergy production, as they are able to provide high yields with low N₂O emissions in the field.     

Multiyear greenhouse gas balances at a rewetted temperate peatland

Drained peat soils are a significant source of greenhouse gas (GHG) emissions to the atmosphere. Rewetting these soils is considered an important climate change mitigation tool to reduce emissions and create suitable conditions for carbon sequestration. Long‐term monitoring is essential to capture interannual variations in GHG emissions and associated environmental variables and to reduce the uncertainty linked with GHG emission factor calculations. In this study, we present GHG balances: carbon dioxide (CO₂), methane (CH₄) and nitrous oxide (N₂O) calculated for a 5‐year period at a rewetted industrial cutaway peatland in Ireland (rewetted 7 years prior to the start of the study); and compare the results with an adjacent drained area (2‐year data set), and with ten long‐term data sets from intact (i.e. undrained) peatlands in temperate and boreal regions. In the rewetted site, CO₂ exchange (or net ecosystem exchange (NEE)) was strongly influenced by ecosystem respiration (R_eco) rather than gross primary production (GPP). CH₄ emissions were related to soil temperature and either water table level or plant biomass. N₂O emissions were not detected in either drained or rewetted sites. Rewetting reduced CO₂ emissions in unvegetated areas by approximately 50%. When upscaled to the ecosystem level, the emission factors (calculated as 5‐year mean of annual balances) for the rewetted site were (±SD) ?104 ± 80 g CO₂‐C m^?2 yr^?1 (i.e. CO₂ sink) and 9 ± 2 g CH₄‐C m^?2 yr^?1 (i.e. CH₄ source). Nearly a decade after rewetting, the GHG balance (100‐year global warming potential) had reduced noticeably (i.e. less warming) in comparison with the drained site but was still higher than comparative intact sites. Our results indicate that rewetted sites may be more sensitive to interannual changes in weather conditions than their more resilient intact counterparts and may switch from an annual CO₂ sink to a source if triggered by slightly drier conditions.     

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

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

Molecular mechanisms of water table lowering and nitrogen deposition in affecting greenhouse gas emissions from a Tibetan alpine wetland

Rapid climate change and intensified human activities have resulted in water table lowering (WTL) and enhanced nitrogen (N) deposition in Tibetan alpine wetlands. These changes may alter the magnitude and direction of greenhouse gas (GHG) emissions, affecting the climate impact of these fragile ecosystems. We conducted a mesocosm experiment combined with a metagenomics approach (GeoChip 5.0) to elucidate the effects of WTL (?20 cm relative to control) and N deposition (30 kg N ha^?1 yr^?1) on carbon dioxide (CO₂), methane (CH₄) and nitrous oxide (N₂O) fluxes as well as the underlying mechanisms. Our results showed that WTL reduced CH₄ emissions by 57.4% averaged over three growing seasons compared with no‐WTL plots, but had no significant effect on net CO₂ uptake or N₂O flux. N deposition increased net CO₂ uptake by 25.2% in comparison with no‐N deposition plots and turned the mesocosms from N₂O sinks to N₂O sources, but had little influence on CH₄ emissions. The interactions between WTL and N deposition were not detected in all GHG emissions. As a result, WTL and N deposition both reduced the global warming potential (GWP) of growing season GHG budgets on a 100‐year time horizon, but via different mechanisms. WTL reduced GWP from 337.3 to ?480.1 g CO₂‐eq m^?2 mostly because of decreased CH₄ emissions, while N deposition reduced GWP from 21.0 to ?163.8 g CO₂‐eq m^?2, mainly owing to increased net CO₂ uptake. GeoChip analysis revealed that decreased CH₄ production potential, rather than increased CH₄ oxidation potential, may lead to the reduction in net CH₄ emissions, and decreased nitrification potential and increased denitrification potential affected N₂O fluxes under WTL conditions. Our study highlights the importance of microbial mechanisms in regulating ecosystem‐scale GHG responses to environmental changes.     

Agricultural encroachment: implications for carbon sequestration in tropical African wetlands

Tropical wetlands have been shown to exhibit high rates of net primary productivity and may therefore play an important role in global climate change mitigation through carbon assimilation and sequestration. Many permanently flooded areas of tropical East Africa are dominated by the highly productive C₄ emergent macrophyte sedge, Cyperus papyrus L. (papyrus). However, increasing population densities around wetland margins in East Africa are reducing the extent of papyrus coverage due to the planting of subsistence crops such as Colocasia esculenta (cocoyam). In this paper, we assess the impact of this land use change on the carbon cycle and in particular the impacts of land conversion on net ecosystem carbon dioxide exchange. Eddy covariance techniques were used, on a campaign basis, to measure fluxes of carbon dioxide over both papyrus and cocoyam dominated wetlands located on the Ugandan shore of Lake Victoria. Peak rates of net photosynthetic CO₂ assimilation, derived from monthly diurnal averages of net ecosystem exchange, of 28–35 μmol CO₂ m^?2 s^?1 and 15–20 μmol CO₂ m^?2 s^?1 were recorded in the papyrus and cocoyam wetlands, respectively, whereas night‐time respiratory losses ranged between 10 and 15 μmol CO₂ m^?2 s^?1 at the papyrus wetland and 5–10 μmol CO₂ m^?2 s^?1 at the cocoyam site. The integration of the flux data suggests that papyrus wetlands have the potential to act as a sink for significant amounts of carbon, in the region of 10 t C ha^?1 yr^?1. The cocoyam vegetation assimilated ~7 t C ha^?1 yr^?1 but when carbon exports from crop biomass removal were accounted for these wetlands represent a significant net loss of carbon of similar magnitude. The development of sustainable wetland management strategies are therefore required to promote the dual wetland function of crop production and the mitigation of greenhouse gas emissions especially under future climate change scenarios.     

The greenhouse gas balance of European grasslands

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

Agricultural greenhouse gas mitigation potential globally,in Europe and in the UK: what have we learnt in the last 20 years?

Agricultural lands occupy about 40–50% of the Earth's land surface. Agricultural practices can make a significant contribution at low cost to increasing soil carbon sinks, reducing greenhouse gas (GHG) emissions and contributing biomass feedstocks for energy use. Considering all gases, the global technical mitigation potential from agriculture (excluding fossil fuel offsets from biomass) by 2030 is estimated to be ca. 5500–6000 Mt CO₂‐eq. yr^?1. Economic potentials are estimated to be 1500–1600, 2500–2700 and 4000–4300 Mt CO₂‐eq. yr^?1 at carbon prices of up to $US20, 50 and 100 t CO₂‐eq.^?1, respectively. The value of the global agricultural GHG mitigation at the same three carbon prices is $US32 000, 130 000 and 420 000 million yr^?1, respectively. At the European level, early estimates of soil carbon sequestration potential in croplands were ca. 200 Mt CO₂ yr^?1, but this is a technical potential and is for geographical Europe as far east as the Urals. The economic potential is much smaller, with more recent estimates for the EU27 suggesting a maximum potential of ca. 20 Mt CO₂‐eq. yr^?1. The UK is small in global terms, but a large part of its land area (11 Mha) is used for agriculture. Agriculture accounts for about 7% of total UK GHG emissions. The mitigation potential of UK agriculture is estimated to be ca. 1–2 Mt CO₂‐eq. yr^?1, accounting for less than 1% of UK total GHG emissions.     

Climatic variability,hydrologic anomaly,and methane emission can turn productive freshwater marshes into net carbon sources

Freshwater marshes are well‐known for their ecological functions in carbon sequestration, but complete carbon budgets that include both methane (CH₄) and lateral carbon fluxes for these ecosystems are rarely available. To the best of our knowledge, this is the first full carbon balance for a freshwater marsh where vertical gaseous [carbon dioxide (CO₂) and CH₄] and lateral hydrologic fluxes (dissolved and particulate organic carbon) have been simultaneously measured for multiple years (2011–2013). Carbon accumulation in the sediments suggested that the marsh was a long‐term carbon sink and accumulated ~96.9 ± 10.3 (±95% CI) g C m^?2 yr^?1 during the last ~50 years. However, abnormal climate conditions in the last 3 years turned the marsh to a source of carbon (42.7 ± 23.4 g C m^?2 yr^?1). Gross ecosystem production and ecosystem respiration were the two largest fluxes in the annual carbon budget. Yet, these two fluxes compensated each other to a large extent and led to the marsh being a CO₂ sink in 2011 (?78.8 ± 33.6 g C m^?2 yr^?1), near CO₂‐neutral in 2012 (29.7 ± 37.2 g C m^?2 yr^?1), and a CO₂ source in 2013 (92.9 ± 28.0 g C m^?2 yr^?1). The CH₄ emission was consistently high with a three‐year average of 50.8 ± 1.0 g C m^?2 yr^?1. Considerable hydrologic carbon flowed laterally both into and out of the marsh (108.3 ± 5.4 and 86.2 ± 10.5 g C m^?2 yr^?1, respectively). In total, hydrologic carbon fluxes contributed ~23 ± 13 g C m^?2 yr^?1 to the three‐year carbon budget. Our findings highlight the importance of lateral hydrologic inflows/outflows in wetland carbon budgets, especially in those characterized by a flow‐through hydrologic regime. In addition, different carbon fluxes responded unequally to climate variability/anomalies and, thus, the total carbon budgets may vary drastically among years.     

Methane oxidation in contrasting soil types: responses to experimental warming with implication for landscape‐integrated CH4 budget

Arctic ecosystems are characterized by a wide range of soil moisture conditions and thermal regimes and contribute differently to the net methane (CH₄) budget. Yet, it is unclear how climate change will affect the capacity of those systems to act as a net source or sink of CH₄. Here, we present results of in situ CH₄ flux measurements made during the growing season 2014 on Disko Island (west Greenland) and quantify the contribution of contrasting soil and landscape types to the net CH₄ budget and responses to summer warming. We compared gas flux measurements from a bare soil and a dry heath, at ambient conditions and increased air temperature, using open‐top chambers (OTCs). Throughout the growing season, bare soil consumed 0.22 ± 0.03 g CH₄‐C m^?2 (8.1 ± 1.2 g CO₂‐eq m^?2) at ambient conditions, while the dry heath consumed 0.10 ± 0.02 g CH₄‐C m^?2 (3.9 ± 0.6 g CO₂‐eq m^?2). These uptake rates were subsequently scaled to the entire study area of 0.15 km², a landscape also consisting of wetlands with a seasonally integrated methane release of 0.10 ± 0.01 g CH₄‐C m^?2 (3.7 ± 1.2 g CO₂‐eq m^?2). The result was a net landscape sink of 12.71 kg CH₄‐C (0.48 tonne CO₂‐eq) during the growing season. A nonsignificant trend was noticed in seasonal CH₄ uptake rates with experimental warming, corresponding to a 2% reduction at the bare soil, and 33% increase at the dry heath. This was due to the indirect effect of OTCs on soil moisture, which exerted the main control on CH₄ fluxes. Overall, the net landscape sink of CH₄ tended to increase by 20% with OTCs. Bare and dry tundra ecosystems should be considered in the net CH₄ budget of the Arctic due to their potential role in counterbalancing CH₄ emissions from wetlands – not the least when taking the future climatic scenarios of the Arctic into account.     

Methane emissions from sheep pasture,measured with an open‐path eddy covariance system

Methane (CH₄) is an important greenhouse gas, contributing 0.4–0.5 W m^?2 to global warming. Methane emissions originate from several sources, including wetlands, rice paddies, termites and ruminating animals. Previous measurements of methane flux from farm animals have been carried out on animals in unnatural conditions, in laboratory chambers or fitted with cumbersome masks. This study introduces eddy covariance measurements of CH₄, using the newly developed LI‐COR LI‐7700 open‐path methane analyser, to measure field‐scale fluxes from sheep grazing freely on pasture. Under summer conditions, fluxes of methane in the morning averaged 30 nmol m^?2 s^?1, whereas those in the afternoon were above 100 nmol m^?2 s^?1, and were roughly two orders of magnitude larger than the small methane emissions from the soil. Methane emissions showed no clear relationship with air temperature or photosynthetically active radiation, but some diurnal pattern was apparent, probably linked to sheep grazing behaviour and metabolism. Over the measurement period (days 60–277, year 2010), cumulative methane fluxes were 0.34 mol CH₄ m^?2, equating to 134.3 g CO₂ equivalents m^?2. By comparison, a carbon dioxide (CO₂) sink of 819 g CO₂ equivalents m^?2 was measured over the same period, but it is likely that much of this would be released back to the atmosphere during the winter or as off‐site losses (through microbial and animal respiration). By dividing methane fluxes by the number of sheep in the field each day, we calculated CH₄ emissions per head of livestock as 7.4 kg CH₄ sheep^?1 yr^?1, close to the published IPCC emission factor of 8 kg CH₄ sheep^?1 yr^?1.     

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

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

High emissions of greenhouse gases from grasslands on peat and other organic soils

Drainage has turned peatlands from a carbon sink into one of the world's largest greenhouse gas (GHG) sources from cultivated soils. We analyzed a unique data set (12 peatlands, 48 sites and 122 annual budgets) of mainly unpublished GHG emissions from grasslands on bog and fen peat as well as other soils rich in soil organic carbon (SOC) in Germany. Emissions and environmental variables were measured with identical methods. Site‐averaged GHG budgets were surprisingly variable (29.2 ± 17.4 t CO₂‐eq. ha^?1 yr^?1) and partially higher than all published data and the IPCC default emission factors for GHG inventories. Generally, CO₂ (27.7 ± 17.3 t CO₂ ha^?1 yr^?1) dominated the GHG budget. Nitrous oxide (2.3 ± 2.4 kg N₂O‐N ha^?1 yr^?1) and methane emissions (30.8 ± 69.8 kg CH₄‐C ha^?1 yr^?1) were lower than expected except for CH₄ emissions from nutrient‐poor acidic sites. At single peatlands, CO₂ emissions clearly increased with deeper mean water table depth (WTD), but there was no general dependency of CO₂ on WTD for the complete data set. Thus, regionalization of CO₂ emissions by WTD only will remain uncertain. WTD dynamics explained some of the differences between peatlands as sites which became very dry during summer showed lower emissions. We introduced the aerated nitrogen stock (N_air) as a variable combining soil nitrogen stocks with WTD. CO₂ increased with N_air across peatlands. Soils with comparatively low SOC concentrations showed as high CO₂ emissions as true peat soils because N_air was similar. N₂O emissions were controlled by the WTD dynamics and the nitrogen content of the topsoil. CH₄ emissions can be well described by WTD and ponding duration during summer. Our results can help both to improve GHG emission reporting and to prioritize and plan emission reduction measures for peat and similar soils at different scales.     

Quantifying global greenhouse gas emissions from land‐use change for crop production

Many assessments of product carbon footprint (PCF) for agricultural products omit emissions arising from land‐use change (LUC). In this study, we developed a framework based on IPCC national greenhouse gas inventory methodologies to assess the impacts of LUC from crop production using oil palm, soybean and oilseed rape as examples. Using ecological zone, climate and soil types from the top 20 producing countries, calculated emissions for transitions from natural vegetation to cropland on mineral soils under typical management ranged from ?4.5 to 29.4 t CO₂‐eq ha^?1 yr^?1 over 20 years for oil palm and 1.2–47.5 t CO₂‐eq ha^?1 yr^?1 over 20 years for soybeans. Oilseed rape showed similar results to soybeans, but with lower maximum values because it is mainly grown in areas with lower C stocks. GHG emissions from other land‐use transitions were between 62% and 95% lower than those from natural vegetation for the arable crops, while conversions to oil palm were a sink for C. LUC emissions were considered on a national basis and also expressed per‐tonne‐of‐oil‐produced. Weighted global averages indicate that, depending on the land‐use transition, oil crop production on newly converted land contributes between ?3.1 and 7.0 t CO₂‐eq t oil production^?1 yr^?1 for palm oil, 11.9–50.6 t CO₂‐eq t oil production^?1 yr^?1 for soybean oil, and 7.7–31.4 t CO₂‐eq t oil production^?1 yr^?1 for rapeseed oil. Assumptions made about crop and LUC distribution within countries contributed up to 66% error around the global averages for natural vegetation conversions. Uncertainty around biomass and soil C stocks were also examined. Finer resolution data and information (particularly on land management and yield) could improve reliability of the estimates but the framework can be used in all global regions and represents an important step forward for including LUC emissions in PCFs.     

Measurement and modelling of CO2 flux from a drained fen peatland cultivated with reed canary grass and spring barley

Cultivation of bioenergy crops has been suggested as a promising option for reduction of greenhouse gas (GHG) emissions from arable organic soils (Histosols). Here, we report the annual net ecosystem exchange (NEE) fluxes of CO₂ as measured with a dynamic closed chamber method at a drained fen peatland grown with reed canary grass (RCG) and spring barley (SB) in a plot experiment (n = 3 for each cropping system). The CO₂ flux was partitioned into gross photosynthesis (GP) and ecosystem respiration (R_E). For the data analysis, simple yet useful GP and R_E models were developed which introduce plot‐scale ratio vegetation index as an active vegetation proxy. The GP model captures the effect of temperature and vegetation status, and the R_E model estimates the proportion of foliar biomass dependent respiration (R_fb) in the total R_E. Annual R_E was 1887 ± 7 (mean ± standard error, n = 3) and 1288 ± 19 g CO₂‐C m^?2 in RCG and SB plots, respectively, with R_fb accounting for 32 and 22% respectively. Total estimated annual GP was ?1818 ± 42 and ?1329 ± 66 g CO₂‐C m^?2 in RCG and SB plots leading to a NEE of 69 ± 36 g CO₂‐C m^?2 yr^?1 in RCG plots (i.e., a weak net source) and ?41 ± 47 g CO₂‐C m^?2 yr^?1 in SB plots (i.e., a weak net sink). Standard errors related to spatial variation were small (as shown above), but more significant uncertainties were related to the modelling approach for establishment of annual budgets. In conclusion, the bioenergy cropping system was not more favourable than the food cropping system when looking at the atmospheric CO₂ emissions during cultivation. However, in a broader GHG life‐cycle perspective, the lower fertilizer N input and the higher biomass yield in bioenergy cropping systems could be beneficial.