Environmental impacts of bioenergy wood production from poplar short‐rotation coppice grown at a marginal agricultural site in Germany

For avoiding competition with food production, marginal land is economically and environmentally highly attractive for biomass production with short‐rotation coppices (SRCs) of fast‐growing tree species such as poplars. Herein, we evaluated the environmental impacts of technological, agronomic, and environmental aspects of bioenergy production from hybrid poplar SRC cultivation on marginal land in southern Germany. For this purpose, different management regimes were considered within a 21‐year lifetime (combining measurements and modeling approaches) by means of a holistic Life Cycle Assessment (LCA). We analyzed two coppicing rotation lengths (7 × 3 and 3 × 7 years) and seven nitrogen fertilization rates and included all processes starting from site preparation, planting and coppicing, wood chipping, and heat production up to final stump removal. The 7‐year rotation cycles clearly resulted in higher biomass yields and reduced environmental impacts such as nitrate (NO₃) leaching and soil nitrous oxide (N₂O) emissions. Fertilization rates were positively related to enhanced biomass accumulation, but these benefits did not counterbalance the negative impacts on the environment due to increased nitrate leaching and N₂O emissions. Greenhouse gas (GHG) emissions associated with the heat production from poplar SRC on marginal land ranged between 8 and 46 kg CO₂‐eq. GJ^?1 (or 11–57 Mg CO₂‐eq. ha^?1). However, if the produced wood chips substitute oil heating, up to 123 Mg CO₂‐eq. ha^?1 can be saved, if produced in a 7‐year rotation without fertilization. Dissecting the entire bioenergy production chain, our study shows that environmental impacts occurred mainly during combustion and storage of wood chips, while technological aspects of establishment, harvesting, and transportation played a negligible role.     

CO2 uptake is offset by CH4 and N2O emissions in a poplar short‐rotation coppice

The need for renewable energy sources will lead to a considerable expansion in the planting of dedicated fast‐growing biomass crops across Europe. These are commonly cultivated as short‐rotation coppice (SRC), and currently poplar (Populus spp.) is the most widely planted. In this study, we report the greenhouse gas (GHG) fluxes of carbon dioxide (CO₂), methane (CH₄) and nitrous oxide (N₂O) measured using eddy covariance technique in an SRC plantation for bioenergy production. Measurements were made during the period 2010–2013, that is, during the first two rotations of the SRC. The overall GHG balance of the 4 years of the study was an emission of 1.90 (±1.37) Mg CO₂eq ha^?1; this indicated that soil trace gas emissions offset the CO₂ uptake by the plantation. CH₄ and N₂O contributed almost equally to offset the CO₂ uptake of ?5.28 (±0.67) Mg CO₂eq ha^?1 with an overall emission of 3.56 (±0.35) Mg CO₂eq ha^?1 of N₂O and of 3.53 (±0.85) Mg CO₂eq ha^?1 of CH₄. N₂O emissions mostly occurred during one single peak a few months after the site was converted to SRC; this peak comprised 44% of the total N₂O loss during the two rotations. Accurately capturing emission events proved to be critical for deriving correct estimates of the GHG balance. The nitrogen (N) content of the soil and the water table depth were the two drivers that best explained the variability in N₂O and CH_4, respectively. This study underlines the importance of the ‘non‐CO₂ GHGs’ on the overall balance. Further long‐term investigations of soil trace gas emissions should monitor the N content and the mineralization rate of the soil, as well as the microbial community, as drivers of the trace gas emissions.     

Can biochar reduce soil greenhouse gas emissions from a Miscanthus bioenergy crop?

Energy production from bioenergy crops may significantly reduce greenhouse gas (GHG) emissions through substitution of fossil fuels. Biochar amendment to soil may further decrease the net climate forcing of bioenergy crop production, however, this has not yet been assessed under field conditions. Significant suppression of soil nitrous oxide (N₂O) and carbon dioxide (CO₂) emissions following biochar amendment has been demonstrated in short‐term laboratory incubations by a number of authors, yet evidence from long‐term field trials has been contradictory. This study investigated whether biochar amendment could suppress soil GHG emissions under field and controlled conditions in a Miscanthus × Giganteus crop and whether suppression would be sustained during the first 2 years following amendment. In the field, biochar amendment suppressed soil CO₂ emissions by 33% and annual net soil CO₂ equivalent (eq.) emissions (CO₂, N₂O and methane, CH₄) by 37% over 2 years. In the laboratory, under controlled temperature and equalised gravimetric water content, biochar amendment suppressed soil CO₂ emissions by 53% and net soil CO₂ eq. emissions by 55%. Soil N₂O emissions were not significantly suppressed with biochar amendment, although they were generally low. Soil CH₄ fluxes were below minimum detectable limits in both experiments. These findings demonstrate that biochar amendment has the potential to suppress net soil CO₂ eq. emissions in bioenergy crop systems for up to 2 years after addition, primarily through reduced CO₂ emissions. Suppression of soil CO₂ emissions may be due to a combined effect of reduced enzymatic activity, the increased carbon‐use efficiency from the co‐location of soil microbes, soil organic matter and nutrients and the precipitation of CO₂ onto the biochar surface. We conclude that hardwood biochar has the potential to improve the GHG balance of bioenergy crops through reductions in net soil CO₂ eq. emissions.     

Land use of drained peatlands: Greenhouse gas fluxes,plant production,and economics

Drained peatlands are hotspots for greenhouse gas (GHG) emissions, which could be mitigated by rewetting and land use change. We performed an ecological/economic analysis of rewetting drained fertile peatlands in a hemiboreal climate using different land use strategies over 80 years. Vegetation, soil processes, and total GHG emissions were modeled using the CoupModel for four scenarios: (1) business as usual—Norway spruce with average soil water table of ?40 cm; (2) willow with groundwater at ?20 cm; (3) reed canary grass with groundwater at ?10 cm; and (4) a fully rewetted peatland. The predictions were based on previous model calibrations with several high‐resolution datasets consisting of water, heat, carbon, and nitrogen cycling. Spruce growth was calibrated by tree‐ring data that extended the time period covered. The GHG balance of four scenarios, including vegetation and soil, were 4.7, 7.1, 9.1, and 6.2 Mg CO₂eq ha^?1 year^?1, respectively. The total soil emissions (including litter and peat respiration CO₂ + N₂O + CH₄) were 33.1, 19.3, 15.3, and 11.0 Mg CO₂eq ha^?1 year^?1, respectively, of which the peat loss contributed 35%, 24%, and 7% of the soil emissions for the three drained scenarios, respectively. No peat was lost for the wet peatland. It was also found that draining increases vegetation growth, but not as drastically as peat respiration does. The cost–benefit analysis (CBA) is sensitive to time frame, discount rate, and carbon price. Our results indicate that the net benefit was greater with a somewhat higher soil water table and when the peatland was vegetated with willow and reed canary grass (Scenarios 2 and 3). We conclude that saving peat and avoiding methane release using fairly wet conditions can significantly reduce GHG emissions, and that this strategy should be considered for land use planning and policy‐making.     

Soil N2O emissions with different reduced tillage methods during the establishment of Miscanthus in temperate grassland

An increase in renewable energy and the planting of perennial bioenergy crops is expected in order to meet global greenhouse gas (GHG) targets. Nitrous oxide (N₂O) is a potent greenhouse gas, and this paper addresses a knowledge gap concerning soil N₂O emissions over the possible “hot spot” of land use conversion from established pasture to the biofuel crop Miscanthus. The work aims to quantify the impacts of this land use change on N₂O fluxes using three different cultivation methods. Three replicates of four treatments were established: Miscanthus x giganteus (Mxg) planted without tillage; Mxg planted with light tillage; a novel seed‐based Miscanthus hybrid planted with light tillage under bio‐degradable mulch film; and a control of uncultivated established grass pasture with sheep grazing. Soil N₂O fluxes were recorded every 2 weeks using static chambers starting from preconversion in April 2016 and continuing until the end of October 2017. Monthly soil samples were also taken and analysed for nitrate and ammonium. There was no significant difference in N₂O emissions between the different cultivation methods. However, in comparison with the uncultivated pasture, N₂O emissions from the cultivated Miscanthus plots were 550%–819% higher in the first year (April to December 2016) and 469%–485% higher in the second year (January to October 2017). When added to an estimated carbon cost for production over a 10 year crop lifetime (including crop management, harvest, and transportation), the measured N₂O conversion cost of 4.13 Mg CO₂‐eq./ha represents a 44% increase in emission compared to the base case. This paper clearly shows the need to incorporate N₂O fluxes during Miscanthus establishment into assessments of GHG balances and life cycle analysis and provides vital knowledge needed for this process. This work therefore also helps to support policy decisions regarding the costs and benefits of land use change to Miscanthus.     

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.     

Greenhouse gas fluxes over managed grasslands in Central Europe

Central European grasslands are characterized by a wide range of different management practices in close geographical proximity. Site‐specific management strategies strongly affect the biosphere–atmosphere exchange of the three greenhouse gases (GHG) carbon dioxide (CO₂), nitrous oxide (N₂O), and methane (CH₄). The evaluation of environmental impacts at site level is challenging, because most in situ measurements focus on the quantification of CO₂ exchange, while long‐term N₂O and CH₄ flux measurements at ecosystem scale remain scarce. Here, we synthesized ecosystem CO₂, N₂O, and CH₄ fluxes from 14 managed grassland sites, quantified by eddy covariance or chamber techniques. We found that grasslands were on average a CO₂ sink (−1,783 to −91 g CO₂ m⁻² year⁻¹), but a N₂O source (18–638 g CO₂‐eq. m⁻² year⁻¹), and either a CH₄ sink or source (−9 to 488 g CO₂‐eq. m⁻² year⁻¹). The net GHG balance (NGB) of nine sites where measurements of all three GHGs were available was found between −2,761 and −58 g CO₂‐eq. m⁻² year⁻¹, with N₂O and CH₄ emissions offsetting concurrent CO₂ uptake by on average 21 ± 6% across sites. The only positive NGB was found for one site during a restoration year with ploughing. The predictive power of soil parameters for N₂O and CH₄ fluxes was generally low and varied considerably within years. However, after site‐specific data normalization, we identified environmental conditions that indicated enhanced GHG source/sink activity (“sweet spots”) and gave a good prediction of normalized overall fluxes across sites. The application of animal slurry to grasslands increased N₂O and CH₄ emissions. The N₂O‐N emission factor across sites was 1.8 ± 0.5%, but varied considerably at site level among the years (0.1%–8.6%). Although grassland management led to increased N₂O and CH₄ emissions, the CO₂ sink strength was generally the most dominant component of the annual GHG budget.     

The Environmental Foodprint of Obesity

Emissions of greenhouse gases (GHG) are linked to global warming and adverse climate changes. Meeting the needs of the increasing number of people on the planet presents a challenge for reducing total GHG burden. A further challenge may be the size of the average person on the planet and the increasing number of people with excess body weight. We used data on GHG emissions from various sources and estimated that obesity is associated with ~20% greater GHG emissions compared with the normal‐weight state. On a global scale, obesity contributes to an extra GHG emissions of ~49 megatons per year of CO₂ equivalent (CO₂eq) from oxidative metabolism due to greater metabolic demands, ~361 megatons per year of CO₂eq from food production processes due to increased food intake, and ~290 megatons per year of CO₂eq from automobile and air transportation due to greater body weight. Therefore, the total impact of obesity may be extra emissions of ~700 megatons per year of CO₂eq, which is about 1.6% of worldwide GHG emissions. Inasmuch as obesity is an important contributor to global GHG burden, strategies to reduce its prevalence should prioritize efforts to reduce GHG emissions. Accordingly, reducing obesity may have considerable benefits for both public health and the environment.     

Life Cycle Greenhouse Gas Emissions Reduction From Rigid Thermal Insulation Use in Buildings

Thermal insulation is a strategic product for reducing energy consumption and related greenhouse gas (GHG) emissions from the building sector. This study examines from a life cycle perspective the changes in GHG emissions resulting from the use of two rigid thermal insulation products manufactured and installed from 1971 to 2025. GHG emissions related to insulation production and fugitive releases of blowing agents are modeled and compared with GHG savings from reduced heating loads in North America, Europe, and Asia. Implementation of alternative blowing agents has greatly improved the carbon dioxide 100‐year equivalent (CO₂‐eq) emission performance of thermal insulation. The net average CO₂‐eq savings to emissions ratio for current extruded polystyrene (XPS) and polyisocyanurate (PIR) insulation studied was 48:1, with a broad range from 3 to 1,800. Older insulation products manufactured with chlorofluorocarbons (CFCs) can result in net cumulative GHG emissions. Reduction of CO₂‐eq emissions from buildings is governed by complex interactions between insulation thickness and placement, climate, fuel type, and heating system efficiencies. A series of charts mapping both emissions payback and net savings demonstrate the interactions between these factors and provide a basis for specific policy recommendations to guide effective insulation investments and placement.     

Balancing conservation and climate change – a methodology using existing data demonstrated for twelve UK priority habitats

Mitigation of climate change (CC) is a regulating ecosystem service provided by priority habitats that is often co-delivered alongside their conservation of biodiversity. Carefully planned conservation management is thought necessary to support biodiversity adaptation to CC, but could also contribute to CC mitigation. This paper presents a methodology for assessing direct emissions of greenhouse gases (GHG: CO₂, CH₄ and N₂O) from 12 UK priority habitats in 26 Special Areas of Conservation (SAC) using readily available data. Background emissions are estimated on the basis of published field research. The contribution of conservation management to GHG emission reduction is estimated using the IPCC GHG accounting methodology and other methods. Management Data Acquisition surveys carried out at selected SACs provided data on management practises for Scotland and Wales. Climate change mitigation actions identified in this study for priority habitats included livestock removal or change in stocking density, with GHG reduction potential of up to 3 tCO₂e/animal/year, afforestation of acid grasslands—up to 19.4 tCO₂e/ha/year, wetland restoration—0.3–0.8 tCO₂e/ha/year and cessation of moorland burning—6.9 tCO₂e/ha/year. Estimated GHG emissions from priority habitats can be used to identify win:win management options that co-deliver GHG mitigation, climate adaptation and conservation benefits for consideration by policy makers and conservation managers.     

Life cycle assessment of eucalyptus short rotation coppices for bioenergy production in southern France

Short rotation coppices (SRC) are considered prime candidates for biomass production, yielding good‐quality feedstock that is easy to harvest. Besides technical, social and economical aspects, environmental issues are important to be taken into account when developing SRC. Here, we evaluated the environmental impacts of delivering 1 GJ of heat from eucalyptus SRC using life cycle assessment (LCA), based on management scenarios involving different rotations lengths, fertilizer input rates, stem densities and harvest methods. Compared to equivalent fossil chains, all eucalyptus scenarios achieved savings of fossil energy and greenhouse gas (GHG) emissions in the 80–90% range, and had generally lower impacts, except for eutrophication. The 3 year rotation scenario was the most energy and GHG‐intensive, whereas manual felling for the longer rotations resulted in twofold larger photochemical ozone impacts compared to the other scenarios. Transportation of wood chips and fertilization were the top two contributors to the impacts, the latter being more important with the shorter rotation lengths due to the evergreen character of eucalyptus. The possibility of including ecosystem carbon dynamics was also investigated, by translating the temporary sequestration of atmospheric CO₂ in the above and belowground biomass of eucalyptus as CO₂ savings using various published equivalence factors. This offset the life cycle GHG emissions of heat provision from eucalyptus SRC by 70–400%.     

Soil GHG fluxes are altered by N deposition: New data indicate lower N stimulation of the N2O flux and greater stimulation of the calculated C pools

The effects of nitrogen (N) deposition on soil organic carbon (C) and greenhouse gas (GHG) emissions in terrestrial ecosystems are the main drivers affecting GHG budgets under global climate change. Although many studies have been conducted on this topic, we still have little understanding of how N deposition affects soil C pools and GHG budgets at the global scale. We synthesized a comprehensive dataset of 275 sites from multiple terrestrial ecosystems around the world and quantified the responses of the global soil C pool and GHG fluxes induced by N enrichment. The results showed that the soil organic C concentration and the soil CO₂, CH₄ and N₂O emissions increased by an average of 3.7%, 0.3%, 24.3% and 91.3% under N enrichment, respectively, and that the soil CH₄ uptake decreased by 6.0%. Furthermore, the percentage increase in N₂O emissions (91.3%) was two times lower than that (215%) reported by Liu and Greaver (Ecology Letters, 2009, 12:1103–1117). There was also greater stimulation of soil C pools (15.70 kg C ha^?1 year^?1 per kg N ha^?1 year^?1) than previously reported under N deposition globally. The global N deposition results showed that croplands were the largest GHG sources (calculated as CO₂ equivalents), followed by wetlands. However, forests and grasslands were two important GHG sinks. Globally, N deposition increased the terrestrial soil C sink by 6.34 Pg CO₂/year. It also increased net soil GHG emissions by 10.20 Pg CO₂‐Geq (CO₂ equivalents)/year. Therefore, N deposition not only increased the size of the soil C pool but also increased global GHG emissions, as calculated by the global warming potential approach.     

Carbon and nitrogen dynamics in bioenergy ecosystems: 2. Potential greenhouse gas emissions and global warming intensity in the conterminous United States

This study estimated the potential emissions of greenhouse gases (GHG) from bioenergy ecosystems with a biogeochemical model AgTEM, assuming maize (Zea mays L.), switchgrass (Panicum virgatum L.), and Miscanthus (Miscanthus × giganteus) will be grown on the current maize‐producing areas in the conterminous United States. We found that the maize ecosystem acts as a mild net carbon source while cellulosic ecosystems (i.e., switchgrass and Miscanthus) act as mild sinks. Nitrogen fertilizer use is an important factor affecting biomass production and N₂O emissions, especially in the maize ecosystem. To maintain high biomass productivity, the maize ecosystem emits much more GHG, including CO₂ and N₂O, than switchgrass and Miscanthus ecosystems, when high‐rate nitrogen fertilizers are applied. For maize, the global warming potential (GWP) amounts to 1–2 Mg CO₂eq ha^?1 yr^?1, with a dominant contribution of over 90% from N₂O emissions. Cellulosic crops contribute to the GWP of less than 0.3 Mg CO₂eq ha^?1 yr^?1. Among all three bioenergy crops, Miscanthus is the most biofuel productive and the least GHG intensive at a given cropland. Regional model simulations suggested that substituting Miscanthus for maize to produce biofuel could potentially save land and reduce GHG emissions.     

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.     

Straw utilization for biofuel production: A consequential assessment of greenhouse gas emissions from bioethanol and biomethane provision with a focus on the time dependency of emissions

The shift from straw incorporation to biofuel production entails emissions from production, changes in soil organic carbon (SOC) and through the provision of (co‐)products and entailed displacement effects. This paper analyses changes in greenhouse gas (GHG) emissions arising from the shift from straw incorporation to biomethane and bioethanol production. The biomethane concept comprises comminution, anaerobic digestion and amine washing. It additionally provides an organic fertilizer. Bioethanol production comprises energetic use of lignin, steam explosion, enzymatic hydrolysis and co‐fermentation. Additionally, feed is provided. A detailed consequential GHG balance with in‐depth focus on the time dependency of emissions is conducted: (a) the change in the atmospheric load of emissions arising from the change in the temporal occurrence of emissions comparing two steady states (before the shift and once a new steady state has established); and (b) the annual change in overall emissions over time starting from the shift are assessed. The shift from straw incorporation to biomethane production results in net changes in GHG emissions of (a) ?979 (?436 to ?1,654) and (b) ?955 (?220 to ?1,623) kg CO₂‐eq. per t_{dry matter} straw converted to biomethane (minimum and maximum). The shift to bioethanol production results in net changes of (a) ?409 (?107 to ?610) and (b) ?361 (57 to ?603) kg CO₂‐eq. per t_{dry matter} straw converted to bioethanol. If the atmospheric load of emissions arising from different timing of emissions is neglected in case (a), the change in GHG emissions differs by up to 54%. Case (b) reveals carbon payback times of 0 (0–49) and 19 (1–100) years in case of biomethane and bioethanol production, respectively. These results demonstrate that the detailed inclusion of temporal aspects into GHG balances is required to get a comprehensive understanding of changes in GHG emissions induced by the introduction of advanced biofuels from agricultural residues.     

Real‐time monitoring of greenhouse gas emissions with tall chambers reveals diurnal N2O variation and increased emissions of CO2 and N2O from Miscanthus following compost addition

Miscanthus x giganteus's efficacy as an energy crop relies on maintaining low greenhouse gas (GHG) emissions. As demand for Miscanthus is expected to rise to meet bioenergy targets, fertilizers and composts may be employed to increase yields, but will also increase GHG emissions. Manipulation experiments are vital to investigate the consequences of any fertilizer additions, but there is currently no way to measure whole‐plant GHG fluxes from crops taller than 2.5 m, such as Miscanthus, at the experimental plot scale. We employed a unique combination of eddy covariance (EC), soil chambers and an entirely new automated chamber system, SkyBeam, to measure high frequency (ca. hourly) fluxes of carbon dioxide (CO₂), methane (CH₄) and nitrous oxide (N₂O) from a Miscanthus crop amended with green compost. Untreated controls were also monitored in a fully replicated experimental design. Net ecosystem exchange (NEE) of CO₂ was partitioned into soil respiration (R_s), gross primary productivity (GPP) and ecosystem respiration, and the crop was harvested to determine the effect of compost on crop productivity. Compost increased NEE emissions by 100% (p < .05), which was the result of a 20% increase of R_s (p < .06) and a 32% reduction in GPP (p < .05) and biomass of 37% (p < .06). Methane fluxes were small and unaffected by compost addition. N₂O emissions increased 34% under compost during an emission event; otherwise, fluxes were low and often negative, even under dry conditions. Diurnal variation in N₂O fluxes, with uptake during the day and emission at night was observed. These fluxes displayed a negative relationship with soil temperature and a hitherto undescribed diurnal temperature hysteresis. We conclude that compost addition negatively affected the productivity and environmental effects of Miscanthus cultivation during the first year following application.     

Measured and modelled effect of land‐use change from temperate grassland to Miscanthus on soil carbon stocks after 12 years

Soil organic carbon (SOC) is an important carbon pool susceptible to land‐use change (LUC). There are concerns that converting grasslands into the C₄ bioenergy crop Miscanthus (to meet demands for renewable energy) could negatively impact SOC, resulting in reductions of greenhouse gas mitigation benefits gained from using Miscanthus as a fuel. This work addresses these concerns by sampling soils (0–30 cm) from a site 12 years (T₁₂) after conversion from marginal agricultural grassland into Miscanthus x giganteus and four other novel Miscanthus hybrids. Soil samples were analysed for changes in below‐ground biomass, SOC and Miscanthus contribution to SOC (using a ¹³C natural abundance approach). Findings are compared to ECOSSE soil carbon model results (run for a LUC from grassland to Miscanthus scenario and continued grassland counterfactual), and wider implications are considered in the context of life cycle assessments based on the heating value of the dry matter (DM) feedstock. The mean T₁₂ SOC stock at the site was 8 (±1 standard error) Mg C/ha lower than baseline time zero stocks (T₀), with assessment of the five individual hybrids showing that while all had lower SOC stock than at T₀ the difference was only significant for a single hybrid. Over the longer term, new Miscanthus C₄ carbon replaces pre‐existing C₃ carbon, though not at a high enough rate to completely offset losses by the end of year 12. At the end of simulated crop lifetime (15 years), the difference in SOC stocks between the two scenarios was 4 Mg C/ha (5 g CO₂‐eq/MJ). Including modelled LUC‐induced SOC loss, along with carbon costs relating to soil nitrous oxide emissions, doubled the greenhouse gas intensity of Miscanthus to give a total global warming potential of 10 g CO₂‐eq/MJ (180 kg CO₂‐eq/Mg DM).     

Non‐native mangroves support carbon storage,sediment carbon burial,and accretion of coastal ecosystems

Mangrove forests play an important role in climate change adaptation and mitigation by maintaining coastline elevations relative to sea level rise, protecting coastal infrastructure from storm damage, and storing substantial quantities of carbon (C) in live and detrital pools. Determining the efficacy of mangroves in achieving climate goals can be complicated by difficulty in quantifying C inputs (i.e., differentiating newer inputs from younger trees from older residual C pools), and mitigation assessments rarely consider potential offsets to CO₂ storage by methane (CH₄) production in mangrove sediments. The establishment of non‐native Rhizophora mangle along Hawaiian coastlines over the last century offers an opportunity to examine the role mangroves play in climate mitigation and adaptation both globally and locally as novel ecosystems. We quantified total ecosystem C storage, sedimentation, accretion, sediment organic C burial and CH₄ emissions from ~70 year old R. mangle stands and adjacent uninvaded mudflats. Ecosystem C stocks of mangrove stands exceeded mudflats by 434 ± 33 Mg C/ha, and mangrove establishment increased average coastal accretion by 460%. Sediment organic C burial increased 10‐fold (to 4.5 Mg C ha^?1 year^?1), double the global mean for old growth mangrove forests, suggesting that C accumulation from younger trees may occur faster than previously thought, with implications for mangrove restoration. Simulations indicate that increased CH₄ emissions from sediments offset ecosystem CO₂ storage by only 2%–4%, equivalent to 30–60 Mg CO₂‐eq/ha over mangrove lifetime (100 year sustained global warming potential). Results highlight the importance of mangroves as novel systems that can rapidly accumulate C, have a net positive atmospheric greenhouse gas removal effect, and support shoreline accretion rates that outpace current sea level rise. Sequestration potential of novel mangrove forests should be taken into account when considering their removal or management, especially in the context of climate mitigation goals.     

Contribution of Urban Water Supply to Greenhouse Gas Emissions in China

Greenhouse gas (GHG) emissions from energy use in the water sector in China have not received the same attention as emissions from other sectors, but interest in this area is growing. This study uses 2011 data to investigate GHG emissions from electricity use for urban water supply in China. The objective is to measure the climate cobenefit of water conservation, compare China with other areas on a number of emissions indicators, and assist in development of policy that promotes low‐emission water supply. Per capita and per unit GHG emissions for water supplied to urban areas in China in 2011 were 24.5 kilograms carbon dioxide equivalent (kg CO₂‐eq) per capita per year and 0.213 kg CO₂‐eq per cubic meter, respectively. Comparison of provinces within China revealed that GHG emissions for urban water supply as a percentage of total province‐wide emissions from electricity use correlate directly with the rate of leakage and water loss within the water distribution system. This highlights controlling leakage as a possible means of reducing the contribution of urban water supply to GHG emissions. An inverse correlation was established between GHG emissions per unit water and average per capita daily water use, which implies that water demand tends to be higher when per unit emissions are lower. China's high emission factor for electricity generation inflates emissions for urban water supply. Shifting from emissions‐intensive electricity sources is crucial to reducing emissions in the water supply sector.     

Conversion of open lands to short‐rotation woody biomass crops: site variability affects nitrogen cycling and N2O fluxes in the US Northern Lake States

Short‐rotation woody biomass crops (SRWC) have been proposed as a major feedstock source for bioenergy generation in the Northeastern US. To quantify the environmental effects and greenhouse gas (GHG) balance of crops including SRWC, investigators need spatially explicit data which encompass entire plantation cycles. A knowledge gap exists for the establishment period which makes current GHG calculations incomplete. In this study, we investigated the effects of converting pasture and hayfields to willow (Salix spp.) and hybrid‐poplar (Populus spp.) SRWC plantations on soil nitrogen (N) cycling, nitrous oxide (N₂O) emissions, and nitrate (NO₃^?) leaching at six sites of varying soil and climate conditions across northern Michigan and Wisconsin, following these plantations from pre conversion through their first 2 years. All six sites responded to establishment with increased N₂O emissions, available inorganic N, and, where it was measured, NO₃^? leaching; however, the magnitude of these impacts varied dramatically among sites. Soil NO₃^? levels varied threefold among sites, with peak extractable NO₃^? concentrations ranging from 15 to 49 g N kg^?1 soil. Leaching losses were significant and persisted through the second year, with 44–112 kg N ha^?1 leached in SRWC plots. N₂O emissions in the first growing season varied 30‐fold among sites, from 0.5 to 17.0 Mg‐CO_2eq ha^?1 (carbon dioxide equivalents). N₂O emissions over 2 years resulted in N₂O emissions due to plantation establishment that ranged from 0.60 to 22.14 Mg‐CO_2eq ha^?1 above baseline control levels across sites. The large N losses we document herein demonstrate the importance of including direct effects of land conversion in life‐cycle analysis (LCA) studies of SRWC GHG balance. Our results also demonstrate the need for better estimation of spatial variability of N cycling processes to quantify the full environmental impacts of SRWC plantations.