Atmospheric methane uptake by tropical montane forest soils and the contribution of organic layers

Microbial oxidation in aerobic soils is the primary biotic sink for atmospheric methane (CH₄), a powerful greenhouse gas. Although tropical forest soils are estimated to globally account for about 28% of annual soil CH₄ consumption (6.2 Tg CH₄ year^?1), limited data are available on CH₄ exchange from tropical montane forests. We present the results of an extensive study on CH₄ exchange from tropical montane forest soils along an elevation gradient (1,000, 2,000, 3,000 m) at different topographic positions (lower slope, mid-slope, ridge position) in southern Ecuador. All soils were net atmospheric CH₄ sinks, with decreasing annual uptake rates from 5.9 kg CH₄–C ha^?1 year^?1 at 1,000 m to 0.6 kg CH₄–C ha^?1 year^?1 at 3,000 m. Topography had no effect on soil atmospheric CH₄ uptake. We detected some unexpected factors controlling net methane fluxes: positive correlations between CH₄ uptake rates, mineral nitrogen content of the mineral soil and with CO₂ emissions indicated that the largest CH₄ uptake corresponded with favorable conditions for microbial activity. Furthermore, we found indications that CH₄ uptake was N limited instead of inhibited by NH₄ ⁺. Finally, we showed that in contrast to temperate regions, substantial high affinity methane oxidation occurred in the thick organic layers which can influence the CH₄ budget of these tropical montane forest soils. Inclusion of elevation as a co-variable will improve regional estimates of methane exchange in these tropical montane forests.     

Carbon dioxide and methane emissions from interfluvial wetlands in the upper Negro River basin, Brazil

Extensive interfluvial wetlands occur in the upper Negro River basin (Brazil) and contain a mosaic of vegetation dominated by emergent grasses and sedges with patches of shrubs and palms. To characterize the release of carbon dioxide and methane from these habitats, diffusive and ebullitive emissions and transport through plant aerenchyma were measured monthly during 2005 in permanently and seasonally flooded areas. CO₂ emissions averaged 2193 mg C m^?2 day^?1. Methane was consumed in unflooded environments and emitted in flooded environments with average values of ?4.8 and 60 mg C m^?2 day^?1, respectively. Bubbles were emitted primarily during falling water periods when hydrostatic pressure at the sediment?Cwater interface declined. CO₂ and CH₄ emissions increased when dissolved O₂ decreased and vegetation was more abundant. Total area and seasonally varying flooded areas for two wetlands, located north and south of the Negro River, were determined through analysis of synthetic aperture radar and optical remotely sensed data. The combined areas of these two wetlands (3000 km²) emitted 1147 Gg C year^?1 as CO₂ and 31 Gg C year^?1 as CH₄. If these rates are extrapolated to the area occupied by hydromorphic soils in the upper Negro basin, 63 Tg C year^?1 of CO₂ and 1.7 Tg C year^?1 as CH₄ are estimated as the regional evasion to the atmosphere.     

Emissions of CO<Subscript>2</Subscript>, CH<Subscript>4</Subscript> and N<Subscript>2</Subscript>O from undisturbed,drained and mined peatlands in Estonia

The aim of this study is to estimate emissions of greenhouse gases CO₂, CH₄ and N₂O, and the effects of drainage and peat extraction on these processes, in Estonian transitional fens and ombrotrophic bogs. Closed-chamber-based sampling lasted from January to December 2009 in nine peatlands in Estonia, covering areas with different land-use practices: natural (four study sites), drained (six sites), abandoned peat mining (five sites) and active peat mining areas (five sites). Median values of soil CO₂ efflux were 1,509, 1,921, 2,845 and 1,741 kg CO₂-C ha^?1 year^?1 from natural, drained, abandoned and active mining areas, respectively. Emission of CH₄-C (median values) was 85.2, 23.7, 0.07 and 0.12 kg ha^?1 year^?1, and N₂O-N ?0.05, ?0.01, 0.18 and 0.19 kg ha^?1 year^?1, respectively. There were significantly higher emissions of CO₂ and N₂O from abandoned and active peat mining areas, whereas CH₄ emissions were significantly higher in natural and drained areas. Significant Spearman rank correlation was found between soil temperature and CO₂ flux at all sites, and CH₄ flux with high water level at natural and drained areas. Significant increase in CH₄ flux was detected for groundwater levels above 30 cm.     

Soil-atmosphere exchange of nitrous oxide and methane in New Zealand terrestrial ecosystems and their mitigation options: a review

The two non-CO₂ greenhouse gases (GHGs) nitrous oxide (N₂O) and methane (CH₄) comprise 54.8% of total New Zealand emissions. Nitrous oxide is mainly generated from mineral N originating from animal dung and urine, applied fertiliser N, biologically fixed N₂, and mineralisation of soil organic N. Even though about 96% of the anthropogenic CH₄ emitted in New Zealand is from ruminant animals (methanogenesis), methane uptake by aerobic soils (methanotrophy) can significantly contribute to the removal of CH₄ from the atmpsphere, as the global estimates confirm. Both the net uptake of CH₄ by soils and N₂O emissions from soils are strongly influenced by changes in land use and land management. Quantitative information on the fluxes of these two non-CO₂ GHGs is required for a range of land-use and land-management ecosystems to determine their contribution to the national emissions inventory, and for assessing the potential of mitigation options. Here we report soil N₂O fluxes and CH₄ uptake for a range of land-use and land-management systems collated from published and unpublished New Zealand studies. Nitrous oxide emissions are highest in dairy-grazed pastures (10–12 kg N₂O–N ha^?1 year^{? 1}), intermediate in sheep-grazed pastures, (4–6 kg N₂O–N ha^?1 year^?1), and lowest in forest, shrubland and ungrazed pasture soils (1–2 kg N₂O–N ha^?1 year^?1). N deposited in the form of animal urine and dung, and N applied as fertiliser, are the principal sources of N₂O production. Generally, N₂O emissions from grazed pasture soils are high when the soil water-filled pore-space is above field capacity, and net CH₄ uptake is low or absent. Although nitrification inhibitors have shown some promise in reducing N₂O emissions from grazed pasture systems, their efficacy as an integral part of farm management has yet to be tested. Methane uptake was highest for a New Zealand Beech forest soil (10–11 kg CH₄ ha^?1 year^?1), intermediate in some pine forest soils (4–6 kg CH₄ ha^?1 year^?1), and lowest in most pasture (<1 kg CH₄ ha^?1 year^?1) and cropped soils (1.5 kg CH₄ ha^?1 year^?1). Afforestation /reforestation of pastures results in increases in soil CH₄ uptake, largely as a result of increases in soil aeration status and changes in the population and activities of methanotrophs. Soil CH₄ uptake is also seasonally dependent, being about two to three times higher in a dry summer and autumn than in a wet winter. There are no practical ways yet available to reduce CH₄ emissions from agricultural systems. The mitigation options to reduce gaseous emissions are discussed and future research needs identified.     

Infilled Ditches are Hotspots of Landscape Methane Flux Following Peatland Re-wetting

Peatlands are large terrestrial stores of carbon, and sustained CO₂ sinks, but over the last century large areas have been drained for agriculture and forestry, potentially converting them into net carbon sources. More recently, some peatlands have been re-wetted by blocking drainage ditches, with the aims of enhancing biodiversity, mitigating flooding, and promoting carbon storage. One potential detrimental consequence of peatland re-wetting is an increase in methane (CH₄) emissions, offsetting the benefits of increased CO₂ sequestration. We examined differences in CH₄ emissions between an area of ditch-drained blanket bog, and an adjacent area where drainage ditches were recently infilled. Results showed that Eriophorum vaginatum colonization led to a “hotspot” of CH₄ emissions from the infilled ditches themselves, with smaller increases in CH₄ from other re-wetted areas. Extrapolated to the area of blanket bog surrounding the study site, we estimated that CH₄ emissions were around 60 kg CH₄ ha^?1 y^?1 prior to drainage, reducing to 44 kg CH₄ ha^?1 y^?1 after drainage. We calculated that fully re-wetting this area would initially increase emissions to a peak of around 120 kg CH₄ ha^?1 y^?1, with around two-thirds of the increase (and 90% of the increase over pre-drainage conditions) attributable to CH₄ emissions from E. vaginatum-colonized infilled ditches, despite these areas only occupying 7% of the landscape. We predicted that emissions should eventually decline toward pre-drainage values as the ecosystem recovers, but only if Sphagnum mosses displace E. vaginatum from the infilled ditches. These results have implications for peatland management for climate change mitigation, suggesting that restoration methods should aim, if possible, to avoid the colonization of infilled ditches by aerenchymatous species such as E. vaginatum, and to encourage Sphagnum establishment.     

A mass-balance study on chloride fluxes in a large central European catchment during 1900–2010

Using data on long-term monitoring of water quality, mass budgets, and empirical models, we quantified chloride (Cl) leaching from major diffuse and point sources in a large central European catchment (upper Vltava river, Czech Republic) over a 110-year period (1900–2010), with the major aim to evaluate the influence of historical changes in land use and management practices on Cl leaching from agricultural land. The Cl input to farmland in synthetic fertilizers, livestock feed, and atmospheric deposition tripled in the 1950s–1980s (from 23 to 64 kg ha^?1 year^?1 on average), and then abruptly decreased to ~14 kg ha^?1 year^?1 during 1990–2010. The proportion of drained agricultural land rapidly increased from 4 % in the 1950s to its maximum of 43 % in the 1990s. Until the 1950s, the Cl leaching from agricultural land followed a simple dose–response function. Then, agricultural soils retained on average 16 ± 4 kg ha^?1 year^?1 of Cl during 1959–1985, when the most important changes in land use and management practices occurred, and subsequently became a net Cl source of 11 ± 3 kg ha^?1 year^?1 on average during 1986–2010, when Cl input to soils declined and drainage of new land ceased. Our data suggest that the temporal changes in the Cl storage in agricultural land are associated with changes in Cl concentrations in both permanent soil water and soils. Physico-chemical conditions in freshly drained soils, namely elevated aeration and high concentrations of soil organic matter (SOM), and high Cl inputs probably resulted in a Cl immobilization in soils by formation of organic chlorine (Cl_org) and adsorption that was higher than the Cl production from Cl_org mineralization and desorption. In contrast, Cl_org mineralization and Cl desorption exceeded the Cl retention during the consecutive period of low Cl inputs and decreasing SOM concentrations in agricultural soils. Our study implies that changes in land use and agricultural management can significantly affect dose–response functions even for Cl, which is traditionally considered and modelled as a conservative ion.     

Net ecosystem carbon exchange and the greenhouse gas balance of tidal marshes along an estuarine salinity gradient

Tidal wetlands are productive ecosystems with the capacity to sequester large amounts of carbon (C), but we know relatively little about the impact of climate change on wetland C cycling in lower salinity (oligohaline and tidal freshwater) coastal marshes. In this study we assessed plant production, C cycling and sequestration, and microbial organic matter mineralization at tidal freshwater, oligohaline, and salt marsh sites along the salinity gradient in the Delaware River Estuary over four years. We measured aboveground plant biomass, carbon dioxide (CO₂) and methane (CH₄) exchange between the marsh and atmosphere, microbial sulfate reduction and methanogenesis in marsh soils, soil biogeochemistry, and C sequestration with radiodating of soils. A simple model was constructed to estimate monthly and annually integrated rates of gross ecosystem production (GEP), ecosystem respiration (ER) to carbon dioxide ( \( {\text{ER}}_{{{\text{CO}}_{2} }} \) ) or methane ( \( {\text{ER}}_{{{\text{CH}}_{4} }} \) ), net ecosystem production (NEP), the contribution of sulfate reduction and methanogenesis to ER, and the greenhouse gas (GHG) source or sink status of the wetland for 2 years (2007 and 2008). All three marsh types were highly productive but evidenced different patterns of C sequestration and GHG source/sink status. The contribution of sulfate reduction to total ER increased along the salinity gradient from tidal freshwater to salt marsh. The Spartina alterniflora dominated salt marsh was a C sink as indicated by both NEP (~140 g C m^?2 year^?1) and ²¹⁰Pb radiodating (336 g C m^?2 year^?1), a minor sink for atmospheric CH₄, and a GHG sink (~620 g CO_2-eq m^?2 year^?1). The tidal freshwater marsh was a source of CH₄ to the atmosphere (~22 g C–CH₄ m^?2 year^?1). There were large interannual differences in plant production and therefore C and GHG source/sink status at the tidal freshwater marsh, though ²¹⁰Pb radiodating indicated modest C accretion (110 g C m^?2 year^?1). The oligohaline marsh site experienced seasonal saltwater intrusion in the late summer and fall (up to 10 mS cm^?1) and the Zizania aquatica monoculture at this site responded with sharp declines in biomass and GEP in late summer. Salinity intrusion was also linked to large effluxes of CH₄ at the oligohaline site (>80 g C–CH₄ m^?2 year^?1), making this site a significant GHG source (>2,000 g CO_2-eq m^?2 year^?1). The oligohaline site did not accumulate C over the 2 year study period, though ²¹⁰Pb dating indicated long term C accumulation (250 g C m^?2 year^?1), suggesting seasonal salt-water intrusion can significantly alter C cycling and GHG exchange dynamics in tidal marsh ecosystems.     

N<Subscript>2</Subscript>O and CH<Subscript>4</Subscript> emission from <Emphasis Type="Italic">Miscanthus</Emphasis> energy crop fields in the infertile Loess Plateau of China

Background

The greenhouse gas (GHG) mitigation is one of the most important environmental benefits of using bioenergy replacing fossil fuels. Nitrous oxide (N₂O) and methane (CH₄) are important GHGs and have drawn extra attention for their roles in global warming. Although there have been many works of soil emissions of N₂O and CH₄ from bioenergy crops in the field scale, GHG emissions in large area of marginal lands are rather sparse and how soil temperature and moisture affect the emission potential remains unknown. Therefore, we sought to estimate the regional GHG emission based on N₂O and CH₄ releases from the energy crop fields.

Results

Here we sampled the top soils from two Miscanthus fields and incubated them using a short-term laboratory microcosm approach under different conditions of typical soil temperatures and moistures. Based on the emission measurements of N₂O and CH₄, we developed a model to estimate annual regional GHG emission of Miscanthus production in the infertile Loess Plateau of China. The results showed that the N₂O emission potential was 0.27 kg N ha^?1 year^?1 and clearly lower than that of croplands and grasslands. The CH₄ uptake potential was 1.06 kg C ha^?1 year^?1 and was slightly higher than that of croplands. Integrated with our previous study on the emission of CO₂, the net greenhouse effect of three major GHGs (N₂O, CH₄ and CO₂) from Miscanthus fields was 4.08 t CO_2eq ha^?1 year^?1 in the Loess Plateau, which was lower than that of croplands, grasslands and shrub lands.

Conclusions

Our study revealed that Miscanthus production may hold a great potential for GHG mitigation in the vast infertile land in the Loess Plateau of China and could contribute to the sustainable energy utilization and have positive environmental impact on the region.

     

Carbon fluxes in forested bog margins along a human impact gradient: could vegetation structure be used as an indicator of peat carbon emissions?

Bog ecosystems are sensitive to anthropogenic disturbance, including drainage and air pollution. Carbon (C) balance measurements to determine the effect of disturbance on bog functioning are laborious; therefore reliable proxies for C fluxes that could facilitate upscaling from single studies to a larger scale would be valuable. We measured peat CO₂ emissions (R _s), CH₄ efflux and vegetation characteristics in four bog areas that formed a gradient from pristine to severely disturbed peatlands, affected by drainage, peat mining, alkaline air pollution and underground oil-shale mining. We expected that sites experiencing higher human impact (i.e., the vegetation was more distinct from that of a natural bog) would have higher R _s and lower CH₄ emissions, but differences in peat C emissions between the most disturbed and pristine sites were not significant. Growing period median R _s ranged from 0.5 to 2.2 g C m^?2 day^?1 for our plots; methane emissions, measured from July to December were an order of magnitude lower, ranging from ?5.9 to 126.7 mg C m^?2 day^?1. R _s and CH₄ emissions were primarily determined by water table depth, as was tree stand productivity. Therefore, stand structural parameters could potentially be good indicators of soil C emissions from poorly drained forested bogs.     

Simulation of N2O emissions and nitrate leaching from plastic mulch radish cultivation with LandscapeDNDC

Radish is one of the major dry field crops in Asia commonly grown with plastic mulch and high rates of N fertilization, and potentially harming the environment due to N₂O emissions and nitrate leaching. Despite the widespread use of plastic mulch, biogeochemical models so far do not yet consider impacts of mulch on soil environmental conditions and biogeochemistry. In this study, we adapted and successfully tested the LandscapeDNDC model against field data by simulating crop growth, C and N turnover and associated N₂O emissions as well as nitrate leaching for radish cultivation with plastic mulch and in conjunction with different rates of N fertilization (465–765 kg N ha^?1 year^?1). Due to the sandy soil texture and monsoon climate, nitrate leaching with rates up to 350 kg N ha^?1 year^?1 was the dominant reason for overall low nitrogen use efficiency (32–43 %). Direct or indirect N₂O emissions (calculated from simulated nitrate leaching rates and IPCC EF_ind = 0.0075) ranged between 2 and 3 kg N ha^?1 year^?1, thus contributing an equal amount to total field emissions of about 5 kg N ha^?1 year^?1. Based on our results, emission factors for direct N₂O emissions ranged between 0.004 and 0.005. These values are only half of the IPCC default value (0.01), demonstrating the need of biogeochemical models for developing site and/or region specific EFs. Simulation results also revealed that changes in agricultural management by applying the fertilizer only to the rows would be an efficient mitigation strategy, effectively decreasing field nitrate leaching and N₂O emissions by 50–60 %.     

Fluxes of nitrogen and phosphorus in a gallery forest in the Cerrado of central Brazil

The Gallery forests of the Cerrado biome play a critical role in controlling stream chemistry but little information about biogeochemical processes in these ecosystems is available. This work describes the fluxes of N and P in solutions along a topographic gradient in a gallery forest. Three distinct floristic communities were identified along the gradient: a wet community nearest the stream, an upland dry community adjacent to the woodland savanna and an intermediate community between the two. Transects were marked in the three communities for sampling. Fluxes of N from bulk precipitation to these forests resulted in deposition of 12.6 kg ha^?1 y^?1 of total N of which 8.8 kg ha^?1 was as inorganic N. The throughfall flux of total N was generally <8.4 kg ha^?1 year^?1. Throughfall NO₃?CN fluxes were higher (7?C32%) while NH₄?CN and organic N fluxes were lower (54?C69% and 5?C46%) than those in bulk precipitation. The throughfall flux was slightly lower for the wet forest community compared to other communities. Litter leachate fluxes differed among floristic communities with higher NH₄?CN in the wet community. The total N flux was greater in the wet forest than in the dry forest (13.5 vs. 9.4 kg ha^?1 year^?1, respectively). The stream water had total N flux of 0.3 kg ha^?1 year^?1. The flux of total P through bulk precipitation was 0.7 kg ha^?1 year^?1 while the mean fluxes of total P in throughfall (0.6 kg ha^?1 year^?1) and litter leachate (0.5 kg ha^?1 year^?1) declined but did not differ between communities. The low concentrations presented in soil solution and low fluxes in stream water (0.3 and 0.1 kg ha^?1 year^?1 for N and P, respectively) relative to other flowpaths emphasize the conservative nutrient cycling of these forests and the importance of internal recycling processes for the maintenance and conservation of riparian and stream ecosystems in the Cerrado.     

Carbon cycling and sequestration in a Japanese red pine (Pinus densiflora) forest on lava flow of Mt. Fuji

Biometric-based carbon flux measurements were conducted in a pine forest on lava flow of Mt. Fuji, Japan, in order to estimate carbon cycling and sequestration. The forest consists mainly of Japanese red pine (Pinus densiflora) in a canopy layer and Japanese holly (Ilex pedunculosa) in a subtree layer. The lava remains exposed on the ground surface, and the soil on the lava flow is still immature with no mineral soil layer. The results showed that the net primary production (NPP) of the forest was 7.3 ± 0.7 t C ha^?1 year^?1, of which 1.4 ± 0.4 t C ha^?1 year^?1 was partitioned to biomass increment, 3.2 ± 0.5 t C ha^?1 year^?1 to above-ground fine litter production, 1.9 t C ha^?1 year^?1 to fine root production, and 0.8 ± 0.2 t C ha^?1 year^?1 to coarse woody debris. The total amount of annual soil surface CO₂ efflux was estimated as 6.1 ± 2.9 t C ha^?1 year^?1, using a closed chamber method. The estimated decomposition rate of soil organic matter, which subtracted annual root respiration from soil respiration, was 4.2 ± 3.1 t C ha^?1 year^?1. Biometric-based net ecosystem production (NEP) in the pine forest was estimated at 2.9 ± 3.2 t C ha^?1 year^?1, with high uncertainty due mainly to the model estimation error of annual soil respiration and root respiration. The sequestered carbon being allocated in roughly equal amounts to living biomass (1.4 t C ha^?1 year^?1) and the non-living C pool (1.5 t C ha^?1 year^?1). Our estimate of biometric-based NEP was 25 % lower than the eddy covariance-based NEP in this pine forest, due partly to the underestimation of NPP and difficulty of estimation of soil and root respiration in the pine forest on lava flows that have large heterogeneity of soil depth. However, our results indicate that the mature pine forest acted as a significant carbon sink even when established on lava flow with low nutrient content in immature soils, and that sequestration strength, both in biomass and in soil organic matter, is large.     

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.     

Methane emissions from Mexican freshwater bodies: correlations with water pollution

The literature concerning methane (CH₄) emissions from temperate and boreal lakes is extensive, but emissions from tropical and subtropical lakes have been less documented. In particular, methane emissions from Mexican lakes, which are often polluted by anthropogenic carbon and nutrient inputs, have not been reported previously. In this work, methane emissions from six Mexican lakes were measured, covering a broad range of organic inputs, trophic states, and climatic conditions. Methane emissions ranged from 5 to 5,000 mg CH₄ m^?2 day^?1. Water samples from several depths in each lake were analyzed for correlation between water quality indicators and methane emissions. Trophic state and water quality indexes were most strongly correlated with methane fluxes. The global methane flux from Mexican freshwater lakes was estimated to be approximately 1.3 Tg CH₄ year^?1, which is about 20% of methane and 4.4% of total national greenhouse gas emissions. Data for untreated wastewater releases to the environment gave an emission factor of 0.19 kg CH₄ kg^?1 of Biochemical Oxygen Demand, which is superior to that previously estimated by the IPCC for lake discharges. Thus, the large volume of untreated wastewater in Mexico implies higher methane emission than previously estimated.     

Soil system budgets of N,Si and P in an agricultural irrigated watershed: surplus,differential export and underlying mechanisms

Ongoing socio-economic and climatic changes can differentially affect the biogeochemistry of the key nutrients nitrogen (N), silica (Si), and phosphorus (P) by altering their soil budgets, their transfer to aquatic environments and their ecological stoichiometry. This may lead to cascade consequences for aquatic communities and biogeochemical processes. Soil budgets, river export, and N, Si, and P ecological stoichiometry were assessed in a heavy impacted basin (Mincio River, Italy) in two decades (1991–2000; 2001–2010). The main aim was to analyse element-specific mechanisms of terrestrial-aquatic transport and retention within aquatic habitats. Budget results suggest a net accumulation (inputs exceeding outputs) of all nutrients in agricultural lands, mainly due to livestock manure, with a reduction for N (196 kg N ha^?1 year^?1 in 2000, and 132 kg N ha^?1 year^?1 in 2010), and constant values for Si (up to 3 kg Si ha^?1 year^?1) and P (43 kg P ha^?1 year^?1) along the study period. River export of N and P accounted for 3–27% and?~?2% of N and P soil net accumulation, respectively, while Si export was significantly greater (25 kg Si ha^?1 year^?1) than Si net accumulation on farmlands. The stoichiometry of net nutrient accumulation in soils was not reflected by the stoichiometry of nutrient riverine export, due to element-specific mechanisms. We speculate that N and Si vertical and horizontal mobilization is increased by the irrigation loop, while P retention is favored by limited erosion due to limited slopes in the Mincio River basin. The simultaneous analysis of N, Si and P allows us to better understand the different paths, transformation and retention mechanisms at the watershed scale.     

Nitrous oxide and methane exchange in two small temperate forest catchments—effects of hydrological gradients and implications for global warming potentials of forest soils

The magnitude of greenhouse gas (GHG) flux rates may be important in wet and intermediate wet forest soils, but published estimates are scarce. We studied the surface exchange of methane (CH₄) and nitrous oxide (N₂O) from soil along toposequences in two temperate deciduous forest catchments: Strødam and Vestskoven. The soil water regime ranged from fully saturated to aerated within the catchments. At Strødam the largest mean flux rates of N₂O (15 μg N₂O-N m^?2 h^?1) were measured at volumetric soil water contents (SWC) between 40 and 60% and associated with low soil pH compared to smaller mean flux rates of 0-5 μg N₂O-N m^?2 h^?1 for drier (SWC < 40%) and wet conditions (SWC > 80%). At Vestskoven the same response of N₂O to soil water content was observed. Average CH₄ flux rates were highly variable along the toposequences (?17 to 536 μg CH₄-C m^?2 h^?1) but emissions were only observed above soil water content of 45%. Scaled flux rates of both GHGs to catchment level resulted in emission of 322 and 211 kg CO₂-equivalents ha^?1 year^?1 for Strødam and Vestskoven, respectively, with N₂O contributing the most at both sites. Although the wet and intermediate wet forest soils occupied less than half the catchment area at both sites, the global warming potential (GWP) derived from N₂O and CH₄ was more than doubled when accounting for these wet areas in the catchments. The results stress the importance of wet soils in assessments of forest soil global warming potentials, as even small proportions of wet soils contributes substantially to the emissions of N₂O and CH₄.     

Soil CO2 efflux and soil carbon balance of a tropical rubber plantation

Natural rubber is a valuable source of income in many tropical countries and rubber trees are increasingly planted in tropical areas, where they contribute to land-use changes that impact the global carbon cycle. However, little is known about the carbon balance of these plantations. We studied the soil carbon balance of a 15-year-old rubber plantation in Thailand and we specifically explored the seasonal dynamic of soil CO₂ efflux (F _S) in relation to seasonal changes in soil water content (W _S) and soil temperature (T _S), assessed the partitioning of F _S between autotrophic (R _A) and heterotrophic (R _H) sources in a root trenching experiment and estimated the contribution of aboveground and belowground carbon inputs to the soil carbon budget. A multiplicative model combining both T _S and W _S explained 58 % of the seasonal variation of F _S. Annual soil CO₂ efflux averaged 1.88 kg C m^?2 year^?1 between May 2009 and April 2011 and R _A and R _H accounted for respectively 63 and 37 % of F _S, after corrections of F _S measured on trenched plots for root decomposition and for difference in soil water content. The 4-year average annual aboveground litterfall was 0.53 kg C m^?2 year^?1 while a conservative estimate of belowground carbon input into the soil was much lower (0.17 kg C m^?2 year^?1). Our results highlighted that belowground processes (root and rhizomicrobial respiration and the heterotrophic respiration related to belowground carbon input into the soil) have a larger contribution to soil CO₂ efflux (72 %) than aboveground litter decomposition.     

Spatial and temporal variability of pCO2 and CO2 efflux in seven Amazonian Rivers

Current estimates of CO₂ outgassing from Amazonian rivers and streams have considerable uncertainty since they are based on limited-time surveys of pCO₂ measurements along the Amazon mainstem and mouths of major tributaries, using conservative estimates of gas exchange velocities. In order to refine basin-scale CO₂ efflux estimates from Amazonian rivers, we present a long time (5-year) dataset of direct measurements of CO₂ fluxes, gas transfer velocities and pCO₂ measurements in seven representative rivers of the lowland Amazon basin fluvial network, six non-tidal (Negro, Solimões, Teles Pires, Cristalino, Araguaia and Javaés) and one tidal river (Caxiuanã), with sizes ranging from 4th to 9th order. Surveys were conducted from January 2006 to December 2010, in a total of 389 campaigns covering all stages of their hydrographs. CO₂ fluxes and gas transfer velocities (k) were measured using floating chambers and pCO₂ was measured simultaneously by headspace extraction followed by gas chromatography analysis. Results show high CO₂ flux rate variability among rivers and hydrograph stages, ranging from ?0.8 to 15.3 μmol CO₂ m^?2 s^?1, with unexpected negative fluxes in clear-water rivers during low waters. Non-tidal rivers showed marked seasonal CO₂ flux patterns, with significantly higher exchange during high waters. Seasonality was modulated by pCO₂, which was positive and strongly correlated with discharge. In these rivers k was well correlated with wind speed, which allowed the use of wind data to model k. We estimate a release of 360 ± 60 Tg C year^?1 from Amazonian rivers and streams within a 1.47 million km² quadrant in the central lowland Amazon. Extrapolating these values to the basin upstream of Óbidos, results in an outgassing of 0.8 Pg C to the atmosphere each year. Our results are a step forward in achieving more accurate gas emission values for Amazonian rivers and their role in the annual carbon budget of the Amazon basin.     

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.     

Estimation of greenhouse gas emissions from sewer pipeline system

Purpose

The aim of this study was to estimate the total greenhouse gas (GHG) emissions generated from whole life cycle stages of a sewer pipeline system and suggest the strategies to mitigate GHG emissions from the system.

Methods

The process-based life cycle assessment (LCA) with a city-scale inventory database of a sewer pipeline system was conducted. The GHG emissions (direct, indirect, and embodied) generated from a sewer pipeline system in Daejeon Metropolitan City (DMC), South Korea, were estimated for a case study. The potential improvement actions which can mitigate GHG emissions were evaluated through a scenario analysis based on a sensitivity analysis.

Results and discussion

The amount of GHG emissions varied with the size (150, 300, 450, 700, and 900 mm) and materials (polyvinyl chloride (PVC), polyethylene (PE), concrete, and cast iron) of the pipeline. Pipes with smaller diameter emitted less GHG, and the concrete pipe generated lower amount of GHG than pipes made from other materials. The case study demonstrated that the operation (OP) stage (3.67 × 10⁴ t CO₂eq year^?1, 64.9%) is the most significant for total GHG emissions (5.65 × 10⁴ t CO₂eq year^?1) because a huge amount of CH₄ (3.51 × 10⁴ t CO₂eq year^?1) can be generated at the stage due to biofilm reaction in the inner surface of pipeline. Mitigation of CH₄ emissions by reducing hydraulic retention time (HRT), optimizing surface area-to-volume (A/V) ratio of pipes, and lowering biofilm reaction during the OP stage could be effective ways to reduce total GHG emissions from the sewer pipeline system. For the rehabilitation of sewer pipeline system in DMC, the use of small diameter pipe, combination of pipe materials, and periodic maintenance activities are suggested as suitable strategies that could mitigate GHG emissions.

Conclusions

This study demonstrated the usability and appropriateness of the process-based LCA providing effective GHG mitigation strategies at a city-scale sewer pipeline system. The results obtained from this study could be applied to the development of comprehensive models which can precisely estimate all GHG emissions generated from sewer pipeline and other urban environmental systems.