Productivity and water use efficiency of Agave americana in the first field trial as bioenergy feedstock on arid lands

Agave species are high‐yielding crassulacean acid metabolism (CAM) plants, some of which are grown commercially and recognized as potential bioenergy species for dry regions of the world. This study is the first field trial of Agave species for bioenergy in the United States, and was established to compare the production of Agave americana with the production of Agave tequilana and Agave fourcroydes, which are produced commercially in Mexico for tequila and fiber. The field trial included four experimental irrigation levels to test the response of biomass production to water inputs. After 3 years, annual production of healthy A. americana plants reached 9.3 Mg dry mass ha^?1 yr^?1 (including pup mass) with 530 mm of annual water inputs, including both rainfall and irrigation. Yields in the most arid conditions tested (300 mm yr^?1 water input) were 2.0–4.0 Mg dry mass ha^?1 yr^?1. Agave tequilana and Agave fourcroydes were severely damaged by cold in the first winter, and produced maximum yields of only 0.04 Mg ha^?1 yr^?1 and 0.26 Mg ha^?1 yr^?1, respectively. The agave snout weevil (Scyphophorus acupunctatus) emerged as an important challenge for A. americana cropping, killing a greater number of plants in the higher irrigation treatments. Physiological differences in A. americana plants across irrigation treatments were most evident in the warmest season, with gas exchange beginning up to 3 h earlier and water use efficiency declining in treatments with the greatest water input (780 mm yr^?1 water input). Yields were lower than previous projections for Agave species, but results from this study suggest that A. americana has potential as a bioenergy crop and would have substantially reduced irrigation requirements relative to conventional crops in the southwestern USA. Challenges for pest management and harvesting must still be addressed before an efficient production system that uses Agave can be realized.     

Marginal land bioethanol yield potential of four crassulacean acid metabolism candidates (Agave fourcroydes,Agave salmiana,Agave tequilana and Opuntia ficus‐indica) in Australia

The Nobel environmental productivity index (EPI) was used as a framework for the development of a predictive geospatial model to estimate the bioethanol yield potential of four crassulacean acid metabolism (CAM) candidates in Australia (Agave fourcroydes, Agave salmiana, Agave tequilana, and Opuntia ficus‐indica). GIS software was used to integrate climate datasets with titratable acidity responses to changes in photosynthetically active radiation (PAR), temperature, and water availability. Additional refinements to Nobel's approach were made to accommodate spatial and temporal fluctuations in soil water potential (ψs) as a function of soil particle size distribution and precipitation, and CO₂ uptake response to a range of day and night temperatures. A scalar factor for CO₂ persistence during periods of drought was also introduced to model the capacity of succulent species of Agave to buffer against fluctuations in ψs. Macro‐scale criteria were applied to estimate environmentally responsible (ER) bioethanol yield potential on lands that are not suitable for food production. Consideration was given to indigenous vascular plant species richness and endemism scores at ER sites of interest. The highest mean ER bioethanol yield was achieved by A. fourcroydes (μ: 3.89, max. 7.17 kL ha^‐1 yr^‐1) while the highest maximum yield was achieved by A. tequilana (μ: 3.78, max. 7.63 kL ha^‐1 yr^‐1). This research indicated the CAM pathway may produce significant yields (≥≥ 5 kL ha^‐1 yr^‐1) at ER sites totalling 57,700 km² (0.7% land area of Australia).     

A reassessment of global bioenergy potential in 2050

Many climate change mitigation strategies rely on strong projected growth in biomass energy, supported by literature estimating high future bioenergy potential. However, expectations to 2050 are highly divergent. Examining the most widely cited studies finds that some assumptions in these models are inconsistent with the best available evidence. By identifying literature‐supported, up‐to‐date assumptions for parameters including crop yields, land availability, and costs, we revise upper‐end estimates of potential biomass availability from dedicated energy crops. Even allowing for the conversion of virtually all ‘unused’ grassland and savannah, we find that the maximum plausible limit to sustainable energy crop production in 2050 would be 40–110 EJ yr^?1. Combined with forestry, crop residues, and wastes, the maximum limit to long‐term total biomass availability is 60–120 EJ yr^?1 in primary energy. After accounting for current trends in bioenergy allocation and conversion losses, we estimate maximum potentials of 10–20 EJ yr^?1 of biofuel, 20–40 EJ yr^?1 of electricity, and 10–30 EJ yr^?1 of heating in 2050. These findings suggest that many technical projections and aspirational goals for future bioenergy use could be difficult or impossible to achieve sustainably.     

Modelling nonlinear dynamics of Crassulacean acid metabolism productivity and water use for global predictions

Crassulacean acid metabolism (CAM) crops are important agricultural commodities in water‐limited environments across the globe, yet modelling of CAM productivity lacks the sophistication of widely used C3 and C4 crop models, in part due to the complex responses of the CAM cycle to environmental conditions. This work builds on recent advances in CAM modelling to provide a framework for estimating CAM biomass yield and water use efficiency from basic principles. These advances, which integrate the CAM circadian rhythm with established models of carbon fixation, stomatal conductance and the soil–plant‐atmosphere continuum, are coupled to models of light attenuation, plant respiration and biomass partitioning. Resulting biomass yield and transpiration for Opuntia ficus‐indica and Agave tequilana are validated against field data and compared with predictions of CAM productivity obtained using the empirically based environmental productivity index. By representing regulation of the circadian state as a nonlinear oscillator, the modelling approach captures the diurnal dynamics of CAM stomatal conductance, allowing the prediction of CAM transpiration and water use efficiency for the first time at the plot scale. This approach may improve estimates of CAM productivity under light‐limiting conditions when compared with previous methods.     

Development and evaluation of ForestGrowth‐SRC a process‐based model for short rotation coppice yield and spatial supply reveals poplar uses water more efficiently than willow

Woody biomass produced from short rotation coppice (SRC) poplar (Populus spp.) and willow (Salix spp.) is a bioenergy feedstock that can be grown widely across temperate landscapes and its use is likely to increase in future. Process‐based models are therefore required to predict current and future yield potential that are spatially resolved and can consider new genotypes and climates that will influence future yield. The development of a process‐based model for SRC poplar and willow, ForestGrowth‐SRC, is described and the ability of the model to predict SRC yield and water use efficiency (WUE) was evaluated. ForestGrowth‐SRC was parameterized from a process‐based model, ForestGrowth for high forest. The new model predicted annual above ground yield well for poplar (r² = 0.91, RMSE = 1.46 ODT ha^?1 yr^?1) and willow (r² = 0.85, RMSE = 1.53 ODT ha^?1 yr^?1), when compared with measured data from seven sites in contrasting climatic zones across the United Kingdom. Average modelled yields for poplar and willow were 10.3 and 9.0 ODT ha^?1 yr^?1, respectively, and interestingly, the model predicted a higher WUE for poplar than for willow: 9.5 and 5.5 g kg^?1 respectively. Using regional mapped climate and soil inputs, modelled and measured yields for willow compared well (r² = 0.58, RMSE = 1.27 ODT ha^?1 yr^?1), providing the first UK map of SRC yield, from a process‐based model. We suggest that the model can be used for predicting current and future SRC yields at a regional scale, highlighting important species and genotype choices with respect to water use efficiency and yield potential.     

Fuzzy GIS‐based multi‐criteria evaluation for US Agave production as a bioenergy feedstock

In the United States, renewable energy mandates calling for increased production of cellulosic biofuels will require a diversity of bioenergy feedstocks to meet growing demands. Within the suite of potential energy crops, plants within the genus Agave promise to be a productive feedstock in hot and arid regions. The potential distributions of Agave tequilana and Agave deserti in the United States were evaluated based on plant growth parameters identified in an extensive literature review. A geospatial suitability model rooted in fuzzy logic was developed that utilized a suite of biophysical criteria to optimize ideal geographic locations for this new crop, and several suitability scenarios were tested for each species. The results of this spatially explicit suitability model suggest that there is potential for Agave to be grown as an energy feedstock in the southwestern region of the United States – particularly in Arizona, California, and Texas – and a significant portion of these areas are proximate to existing transportation infrastructure. Both Agave species showed the highest state‐level renewable energy benefit in Arizona, where agave plants have the potential to contribute 4.8–9.6% of the states' ethanol consumption, and 2.5–4.9% of its electricity consumption, for A. deserti and A. tequilana, respectively. This analysis supports the feasibility of Agave as a complementary bioenergy feedstock that can be grown in areas too harsh for conventional energy feedstocks.     

Trade‐offs between land and water requirements for large‐scale bioenergy production

Bioenergy is expected to play an important role in the future energy mix as it can substitute fossil fuels and contribute to climate change mitigation. However, large‐scale bioenergy cultivation may put substantial pressure on land and water resources. While irrigated bioenergy production can reduce the pressure on land due to higher yields, associated irrigation water requirements may lead to degradation of freshwater ecosystems and to conflicts with other potential users. In this article, we investigate the trade‐offs between land and water requirements of large‐scale bioenergy production. To this end, we adopt an exogenous demand trajectory for bioenergy from dedicated energy crops, targeted at limiting greenhouse gas emissions in the energy sector to 1100 Gt carbon dioxide equivalent until 2095. We then use the spatially explicit global land‐ and water‐use allocation model MAgPIE to project the implications of this bioenergy target for global land and water resources. We find that producing 300 EJ yr^?1 of bioenergy in 2095 from dedicated bioenergy crops is likely to double agricultural water withdrawals if no explicit water protection policies are implemented. Since current human water withdrawals are dominated by agriculture and already lead to ecosystem degradation and biodiversity loss, such a doubling will pose a severe threat to freshwater ecosystems. If irrigated bioenergy production is prohibited to prevent negative impacts of bioenergy cultivation on water resources, bioenergy land requirements for meeting a 300 EJ yr^?1 bioenergy target increase substantially (+ 41%) – mainly at the expense of pasture areas and tropical forests. Thus, avoiding negative environmental impacts of large‐scale bioenergy production will require policies that balance associated water and land requirements.     

Initial soil C and land‐use history determine soil C sequestration under perennial bioenergy crops

In the UK and other temperate regions, short rotation coppice (SRC) and Miscanthus x giganteus (Miscanthus) are two of the leading ‘second‐generation’ bioenergy crops. Grown specifically as a low‐carbon (C) fossil fuel replacement, calculations of the climate mitigation provided by these bioenergy crops rely on accurate data. There are concerns that uncertainty about impacts on soil C stocks of transitions from current agricultural land use to these bioenergy crops could lead to either an under‐ or overestimate of their climate mitigation potential. Here, for locations across mainland Great Britain (GB), a paired‐site approach and a combination of 30‐cm‐ and 1‐m‐deep soil sampling were used to quantify impacts of bioenergy land‐use transitions on soil C stocks in 41 commercial land‐use transitions; 12 arable to SRC, 9 grasslands to SRC, 11 arable to Miscanthus and 9 grasslands to Miscanthus. Mean soil C stocks were lower under both bioenergy crops than under the grassland controls but only significant at 0–30 cm. Mean soil C stocks at 0–30 cm were 33.55 ± 7.52 Mg C ha^?1 and 26.83 ± 8.08 Mg C ha^?1 lower under SRC (P = 0.004) and Miscanthus plantations (P = 0.001), respectively. Differences between bioenergy crops and arable controls were not significant in either the 30‐cm or 1‐m soil cores and smaller than for transitions from grassland. No correlation was detected between change in soil C stock and bioenergy crop age (time since establishment) or soil texture. Change in soil C stock was, however, negatively correlated with the soil C stock in the original land use. We suggest, therefore, that selection of sites for bioenergy crop establishment with lower soil C stocks, most often under arable land use, is the most likely to result in increased soil C stocks.     

Changes in soil carbon stocks under perennial and annual bioenergy crops

Bioenergy crops are expected to provide biomass to replace fossil resources and reduce greenhouse gas emissions. In this context, changes in soil organic carbon (SOC) stocks are of primary importance. The aim of this study was to measure changes in SOC stocks in bioenergy cropping systems comparing perennial (Miscanthus × giganteus and switchgrass), semi‐perennial (fescue and alfalfa), and annual (sorghum and triticale) crops, all established after arable crops. The soil was sampled at the start of the experiment and 5 or 6 years later. SOC stocks were calculated at equivalent soil mass, and δ¹³C measurements were used to calculate changes in new and old SOC stocks. Crop residues found in soil at the time of SOC measurements represented 3.5–7.2 t C ha^?1 under perennial crops vs. 0.1–0.6 t C ha^?1 for the other crops. During the 5‐year period, SOC concentrations under perennial crops increased in the surface layer (0–5 cm) and slightly declined in the lower layers. Changes in δ¹³C showed that C inputs were mainly located in the 0–18 cm layer. In contrast, SOC concentrations increased over time under semi‐perennial crops throughout the old ploughed layer (ca. 0–33 cm). SOC stocks in the old ploughed layer increased significantly over time under semi‐perennials with a mean increase of 0.93 ± 0.28 t C ha^?1 yr^?1, whereas no change occurred under perennial or annual crops. New SOC accumulation was higher for semi‐perennial than for perennial crops (1.50 vs. 0.58 t C ha^?1 yr^?1, respectively), indicating that the SOC change was due to a variation in C input rather than a change in mineralization rate. Nitrogen fertilization rate had no significant effect on SOC stocks. This study highlights the interest of comparing SOC changes over time for various cropping systems.     

Carbon sequestration in soil in a semi‐natural Miscanthus sinensis grassland and Cryptomeria japonica forest plantation in Aso,Kumamoto, Japan

Although Miscanthus sinensis grasslands (Misc‐GL) and Cryptomeria japonica forest plantations (Cryp‐FP) are proposed bioenergy feedstock systems, their relative capacity to sequester C may be an important factor in determining their potential for sustainable bioenergy production. Therefore, our objective was to quantify changes in soil C sequestration 47 years after a Misc‐GL was converted to a Cryp‐FP. The study was conducted on adjacent Misc‐GL and Cryp‐FP located on Mt. Aso, Kumamoto, Japan. After Cryp‐FP establishment, only the Misc‐GL continued to be managed by annual burning every March. Mass C and N, δ¹³C, and δ¹⁵N at 0–30 cm depth were measured in 5 cm increments. Carbon and N concentrations, C:N ratio, δ¹³C, and δ¹⁵N were measured in litter and/or ash, and rhizomes or roots. Although C input in Misc‐GL by M. sinensis was approximately 36% of that in Cryp‐FP by C. japonica, mean annual soil C sequestration in Misc‐GL (503 kg C ha^?1 yr^?1) was higher than that in Cryp‐FP (284 kg C ha^?1 yr^?1). This was likely the result of larger C input from aboveground litter to soil, C‐quality (C:N ratio and lignin concentration in aboveground litter) and possibly more recalcitrant C (charcoal) inputs by annual burning. The difference in soil δ¹⁵N between sites indicated that organic C with N had greater cycling between heterotrophic microbes and soil and produces more recalcitrant humus in Misc‐GL than in Cryp‐FP. Our data indicate that in terms of soil C sequestration, maintenance of Misc‐GL may be more advantageous than conversion to Cryp‐FP in Aso, Japan.     

Plant roots and GHG mitigation in native perennial bioenergy cropping systems

Native perennial bioenergy crops can mitigate greenhouse gases (GHG) by displacing fossil fuels with renewable energy and sequestering atmospheric carbon (C) in soil and roots. The relative contribution of root C to net GHG mitigation potential has not been compared in perennial bioenergy crops ranging in species diversity and N fertility. We measured root biomass, C, nitrogen (N), and soil organic carbon (SOC) in the upper 90 cm of soil for five native perennial bioenergy crops managed with and without N fertilizer. Bioenergy crops ranged in species composition and were annually harvested for 6 (one location) and 7 years (three locations) following the seeding year. Total root biomass was 84% greater in switchgrass (Panicum virgatum L.) and a four‐species grass polyculture compared to high‐diversity polycultures; the difference was driven by more biomass at shallow soil depth (0–30 cm). Total root C (0–90 cm) ranged from 3.7 Mg C ha^?1 for a 12‐species mixture to 7.6 Mg C ha^?1 for switchgrass. On average, standing root C accounted for 41% of net GHG mitigation potential. After accounting for farm and ethanol production emissions, net GHG mitigation potential from fossil fuel offsets and root C was greatest for switchgrass (?8.4 Mg CO2e ha^?1 yr^?1) and lowest for high‐diversity mixtures (?4.5 Mg CO2e ha^?1 yr^?1). Nitrogen fertilizer did not affect net GHG mitigation potential or the contribution of roots to GHG mitigation for any bioenergy crop. SOC did not change and therefore did not contribute to GHG mitigation potential. However, associations among SOC, root biomass, and root C : N ratio suggest greater long‐term C storage in diverse polycultures vs. switchgrass. Carbon pools in roots have a greater effect on net GHG mitigation than SOC in the short‐term, yet variation in root characteristics may alter patterns in long‐term C storage among bioenergy crops.     

Comparative assessment of ecosystem C exchange in Miscanthus and reed canary grass during early establishment

Land‐use change to bioenergy crop production can contribute towards addressing the dual challenges of greenhouse gas mitigation and energy security. Realisation of the mitigation potential of bioenergy crops is, however, dependent on suitable crop selection and full assessment of the carbon (C) emissions associated with land conversion. Using eddy covariance‐based estimates, ecosystem C exchange was studied during the early‐establishment phase of two perennial crops, C₃ reed canary grass (RCG) and C₄ Miscanthus, planted on former grassland in Ireland. Crop development was the main determinant of net carbon exchange in the Miscanthus crop, restricting significant net C uptake during the first 2 years of establishment. The Miscanthus ecosystem switched from being a net C source in the conversion year to a strong net C sink (?411 ± 63 g C m^?2) in the third year, driven by significant above‐ground growth and leaf expansion. For RCG, early establishment and rapid canopy development facilitated a net C sink in the first 2 years of growth (?319 ± 57 (post‐planting) and ?397 ± 114 g C m^?2, respectively). Peak seasonal C uptake occurred three months earlier in RCG (May) than Miscanthus (August), however Miscanthus sustained net C uptake longer into the autumn and was close to C‐neutral in winter. Leaf longevity is therefore a key advantage of C₄ Miscanthus in temperate climates. Further increases in productivity are projected as Miscanthus reaches maturity and are likely to further enhance the C sink potential of Miscanthus relative to RCG.     

Poplar and shrub willow energy crops in the United States: field trial results from the multiyear regional feedstock partnership and yield potential maps based on the PRISM‐ELM model

To increase the understanding of poplar and willow perennial woody crops and facilitate their deployment for the production of biofuels, bioproducts, and bioenergy, there is a need for broadscale yield maps. For national analysis of woody and herbaceous crops production potential, biomass feedstock yield maps should be developed using a common framework. This study developed willow and poplar potential yield maps by combining data from a network of willow and poplar field trials and the modeling power of PRISM‐ELM. Yields of the top three willow cultivars across 17 sites ranged from 3.60 to 14.6 Mg ha^?1 yr^?1 dry weight, while the yields from 17 poplar trials ranged from 7.5 to 15.2 Mg ha^?1 yr^?1. Relationships between the environmental suitability estimates from the PRISM‐ELM model and results from field trials had an R² of 0.60 for poplar and 0.81 for willow. The resulting potential yield maps reflected the range of poplar and willow yields that have been reported in the literature. Poplar covered a larger geographic range than willow, which likely reflects the poplar breeding efforts that have occurred for many more decades using genotypes from a broader range of environments than willow. While the field trial data sets used to develop these models represent the most complete information at the time, there is a need to expand and improve the model by monitoring trials over multiple cutting cycles and across a broader range of environmental gradients. Despite some limitations, the results of these models represent a dramatic improvement in projections of potential yield of poplar and willow crops across the United States.     

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.     

An evaluation of the global potential of bioenergy production on degraded lands

In this article the global potential of energy crop production on degraded lands was estimated using detailed, spatially explicit data about the area, type and extent of degradation derived from the Global Assessment of Land Degradation Dataset, and by combining this dataset with various spatially explicit data sets. Next, an estimate was made of the possible yield of perennial energy crops on the degraded areas as a function of the type and degree of degradation. Lightly degraded areas were not included, as these areas might be suitable for conventional food production. The total global potential energy production on degraded lands was assessed to be slightly above 150 and 190 EJ yr^?1, for grassy and woody energy crops, respectively. Most of this potential, however, is on areas currently classified as forest, cropland or pastoral land, leaving a potential of around 25 and 32 EJ yr^?1 on other land cover categories. Most of the potential energy crop production on degraded land is located in developing regions. China has a total potential of 30 EJ yr^?1, of which 4 EJ yr^?1 from areas classified as other land. Also USA, Brazil, West Africa, East Africa, Russia and India have substantial potentials of 12–18 EJ yr^?1, with up to 30% of the potential from areas classified as other land.     

Comparing annual and perennial crops for bioenergy production – influence on nitrate leaching and energy balance

Production of energy crops is promoted as a means to mitigate global warming by decreasing dependency on fossil energy. However, agricultural production of bioenergy can have various environmental effects depending on the crop and production system. In a field trial initiated in 2008, nitrate concentration in soil water was measured below winter wheat, grass‐clover and willow during three growing seasons. Crop water balances were modelled to estimate the amount of nitrate leached per hectare. In addition, dry matter yields and nitrogen (N) yields were measured, and N balances and energy balances were calculated. In willow, nitrate concentrations were up to approximately 20 mg l^?1 nitrate‐N during the establishment year, but declined subsequently to <5 mg l^?1 nitrate‐N, resulting in an annual N leaching loss of 18, 3 and 0.3 kg ha^?1 yr^?1 N in the first 3 years after planting. A similar trend was observed in grass‐clover where concentrations stabilized at 2–4 mg l^?1 nitrate‐N from the beginning of the second growing season, corresponding to leaching of approximately 5 kg ha^?1 yr^?1 N. In winter wheat, an annual N leaching loss of 36–68 kg ha^?1 yr^?1 was observed. For comparison, nitrate leaching was also measured in an old willow crop established in 1996 from which N leaching ranged from 6 to 27 kg ha^?1 yr^?1. Dry matter yields ranged between 5.9 and 14.8 Mg yr^?1 with lowest yield in the newly established willow and the highest yield harvested in grass‐clover. Grass‐clover gave the highest net energy yield of 244 GJ ha^?1 yr^?1, whereas old willow, winter wheat and first rotation willow gave net energy yields of 235, 180 and 105 GJ ha^?1 yr^?1. The study showed that perennial crops can provide high energy yields and significantly reduce N losses compared to annual crops.     

Bioenergy crop greenhouse gas mitigation potential under a range of management practices

Perennial grasses have been proposed as viable bioenergy crops because of their potential to yield harvestable biomass on marginal lands annually without displacing food and to contribute to greenhouse gas (GHG) reduction by storing carbon in soil. Switchgrass, miscanthus, and restored native prairie are among the crops being considered in the corn and agricultural regions of the Midwest and eastern United States. In this study, we used an extensive dataset of site observations for each of these crops to evaluate and improve the DayCent biogeochemical model and make predictions about how both yield and GHG fluxes would respond to different management practices compared to a traditional corn‐soy rotation. Using this model‐data integration approach, we found 30–75% improvement in our predictions over previous studies and a subsequent evaluation with a synthesis of sites across the region revealed good model‐data agreement of harvested yields (r² > 0.62 for all crops). We found that replacement of corn‐soy rotations would result in a net GHG reduction of 0.5, 1.0, and 2.0 Mg C ha^?1 yr^?1 with average annual yields of 3.6, 9.2, and 17.2 Mg of dry biomass per year for native prairie, switchgrass, and miscanthus respectively. Both the yield and GHG balance of switchgrass and miscanthus were affected by harvest date with highest yields occurring near onset of senescence and highest GHG reductions occurring in early spring before the new crops emergence. Addition of a moderate length rotation (10–15 years) caused less than a 15% change to yield and GHG balance. For policy incentives aimed at GHG reduction through onsite management practices and improvement of soil quality, post‐senescence harvests are a more effective means than maximizing yield potential.     

Changes in isotopic signatures of soil carbon and CO2 respiration immediately and one year after Miscanthus removal

The removal of perennial bioenergy crops, such as Miscanthus, has rarely been studied although it is an important form of land use change. Miscanthus is a C4 plant, and the carbon (C) it deposits during its growth has a different isotopic signature (¹²/¹³C) compared to a C3 plant. Identifying the proportion of C stored and released to the atmosphere is important information for ecosystem models and life cycle analyses. During a removal experiment in June 2011 of a 20‐year old Miscanthus field (Grignon, France), vegetation was removed mechanically and chemically. Two replicate plots were converted into a rotation of annual crops, two plots had Miscanthus removed with no soil disturbance, followed by bare soil (set‐aside), one control plot was left with continued Miscanthus cultivation, and an adjacent field was used as annual arable crops control. There was a significant difference in the isotopic composition of the total soil C under Miscanthus compared with adjacent annual arable crops in all three measured soil layers (0–5, 5–10 and 10–20 cm). Before Miscanthus removal, total C in the soil under Miscanthus ranged from 4.9% in the top layer to 3.9% in the lower layers with δ¹³C values of ?16.3 to ?17.8 while soil C under the adjacent arable crop was significantly lower and ranged from 1.6 to 2% with δ¹³C values of ?23.2. This did not change much in 2012, suggesting the accumulation of soil C under Miscanthus persists for at least the first year. In contrast, the isotopic signals of soil respiration 1 year after Miscanthus removal from recultivated and set‐aside plots were similar to that of the annual arable control, while just after removal the signals were similar to that of the Miscanthus control. This suggests a rapid change in the form of soil C pools that are respired.     

Environmental costs and benefits of growing Miscanthus for bioenergy in the UK

Planting the perennial biomass crop Miscanthus in the UK could offset 2–13 Mt oil eq. yr^?1, contributing up to 10% of current energy use. Policymakers need assurance that upscaling Miscanthus production can be performed sustainably without negatively impacting essential food production or the wider environment. This study reviews a large body of Miscanthus relevant literature into concise summary statements. Perennial Miscanthus has energy output/input ratios 10 times higher (47.3 ± 2.2) than annual crops used for energy (4.7 ± 0.2 to 5.5 ± 0.2), and the total carbon cost of energy production (1.12 g CO₂‐C eq. MJ^?1) is 20–30 times lower than fossil fuels. Planting on former arable land generally increases soil organic carbon (SOC) with Miscanthus sequestering 0.7–2.2 Mg C4‐C ha^?1 yr^?1. Cultivation on grassland can cause a disturbance loss of SOC which is likely to be recovered during the lifetime of the crop and is potentially mitigated by fossil fuel offset. N₂O emissions can be five times lower under unfertilized Miscanthus than annual crops and up to 100 times lower than intensive pasture. Nitrogen fertilizer is generally unnecessary except in low fertility soils. Herbicide is essential during the establishment years after which natural weed suppression by shading is sufficient. Pesticides are unnecessary. Water‐use efficiency is high (e.g. 5.5–9.2 g aerial DM (kg H₂O)^?1, but high biomass productivity means increased water demand compared to cereal crops. The perennial nature and belowground biomass improves soil structure, increases water‐holding capacity (up by 100–150 mm), and reduces run‐off and erosion. Overwinter ripening increases landscape structural resources for wildlife. Reduced management intensity promotes earthworm diversity and abundance although poor litter palatability may reduce individual biomass. Chemical leaching into field boundaries is lower than comparable agriculture, improving soil and water habitat quality.     

A comparison of isoprene and monoterpene emission rates from the perennial bioenergy crops short‐rotation coppice willow and Miscanthus and the annual arable crops wheat and oilseed rape

Biogenic volatile organic compounds (BVOC) emissions from bioenergy crops may differ from those of conventional crops. We compared emission rates of isoprene and a number of monoterpenes from the lignocellulosic bioenergy crops short‐rotation coppice (SRC) willow and Miscanthus, with the conventional crops wheat and oilseed rape. BVOC emission rates were measured via dynamic vegetation enclosure and GC‐MS analysis approximately monthly between April 2010 and August 2012 at a location in England and from SRC willow at two locations in Scotland. The largest BVOC emission rates were measured from willow in England and varied between years. Isoprene emission rates varied between μg g^?1 h^?1. Of the monoterpenes detected from willow, α‐pinene emission rates were highest (μg g^?1 h^?1), followed by μg g^?1 h^?1 for δ‐3‐carene, μg g^?1 h^?1 for β‐pinene and μg g^?1 h^?1 for limonene. BVOC emission rates measured in Scotland were much lower. Low emission rates of isoprene and α‐pinene were measured from Miscanthus in 2010 (μg g^?1 h^?1 and μg g^?1 h^?1, respectively) but were not detected in subsequent years. Emission rates from wheat of isoprene were negligible but relatively high for monoterpenes (μg g^?1 h^?1 and μg g^?1 h^?1 for α‐pinene and limonene, respectively). No significant emission rates of BVOCs were measured from oilseed rape. The measured emission rates followed a clear seasonal trend. Crude extrapolations based solely on data gathered here indicate that isoprene emissions from willow could correspond to 0.004–0.03% (UK) and 0.76–5.5% (Europe) of current global isoprene if 50% of all land potentially available for bioenergy crops is planted with willow.