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.     

Where can switchgrass production be more profitable than corn and soybean? An integrated subfield assessment in Iowa,USA

Perennial bioenergy crops are considered an important feedstock for a growing bioeconomy. However, in the USA, production of biofuel from these dedicated, nonfood crops is lagging behind federal mandates and markets have yet to develop. Most studies on the economic potential of perennial biofuel crops have concluded that even high‐yielding bioenergy grasses are unprofitable compared to corn/soybeans, the prevailing crops in the United States Corn Belt. However, they did not account for opportunities precision agriculture presents to integrate perennials into agronomically and economically underperforming parts of corn/soybean fields. Using publicly available subfield data and market projections, we identified an upper bound to the areas in Iowa, United States, where the conversion from corn/soybean cropland to an herbaceous bioenergy crop, switchgrass, could be economically viable under different price, land tenancy, and yield scenarios. Assuming owned land, medium crop prices, and a biomass price of US$ 55 Mg^?1, we showed that 4.3% of corn/soybean cropland could break even when converted to switchgrass yielding up to 10.08 Mg ha^?1. The annualized change in net present value on each converted subfield patch ranged from just above US$ 0 ha^?1 to 692 ha^?1. In the three counties of highest economic opportunity, total annualized producer benefits from converting corn/soybean to switchgrass summed to US$ 2.6 million, 3.4 million, and 7.6 million, respectively. This is the first study to quantify an upper bound to the potential private economic benefits from targeted conversion of unfavorable corn/soybean cropland to switchgrass, leaving arable land already under perennial cover unchanged. Broadly, we conclude that areas with high within‐field yield variation provide highest economic opportunities for switchgrass conversion. Our results are relevant for policy design intended to improve the sustainability of agricultural production. While focused on Iowa, this approach is applicable to other intensively farmed regions globally with similar data availability.     

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 integrated biogeochemical and economic analysis of bioenergy crops in the Midwestern United States

This study integrates a biophysical model with a county‐specific economic analysis of breakeven prices of bioenergy crop production to assess the biophysical and economic potential of biofuel production in the Midwestern United States. The bioenergy crops considered in this study include a genotype of Miscanthus, Miscanthus×giganteus, and the Cave‐in‐Rock breed of switchgrass (Panicum virgatum). The estimated average peak biomass yield for miscanthus in the Midwestern states ranges between 7 and 48 metric tons dry matter per hectare per year ( t DM ha^?1 yr^?1), while that for switchgrass is between 10 and 16 t DM ha^?1 yr^?1. With the exception of Minnesota and Wisconsin, where miscanthus yields are likely to be low due to cold soil temperatures, the yield of miscanthus is on average more than two times higher than yield of switchgrass. We find that the breakeven price, which includes the cost of producing the crop and the opportunity cost of land, of producing miscanthus ranges from $53 t^?1 DM in Missouri to $153 t^?1 DM in Minnesota in the low‐cost scenario. Corresponding costs for switchgrass are $88 t^?1 DM in Missouri to $144 t^?1 DM in Minnesota. In the high‐cost scenario, the lowest cost for miscanthus is $85 t^?1 DM and for switchgrass is $118 t^?1 DM, both in Missouri. These two scenarios differ in their assumptions about ease of establishing the perennial crops, nutrient requirements and harvesting costs and losses. The differences in the breakeven prices across states and across crops are mainly driven by bioenergy and row crop yields per hectare. Our results suggest that while high yields per unit of land of bioenergy crops are critical for the competitiveness of bioenergy feedstocks, the yields of the row crops they seek to displace are also an important consideration. Even high yielding crops, such as miscanthus, are likely to be economically attractive only in some locations in the Midwest given the high yields of corn and soybean in the region.     

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.     

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

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

Crassulacean acid metabolism (CAM) offers sustainable bioenergy production and resilience to climate change

Biomass production on low‐grade land is needed to meet future energy demands and minimize resource conflicts. This, however, requires improvements in plant water‐use efficiency (WUE) that are beyond conventional C3 and C4 dedicated bioenergy crops. Here we present the first global‐scale geographic information system (GIS)‐based productivity model of two highly water‐efficient crassulacean acid metabolism (CAM) candidates: Agave tequilana and Opuntia ficus‐indica. Features of these plants that translate to WUE advantages over C3 and C4 bioenergy crops include nocturnal stomatal opening, rapid rectifier‐like root hydraulic conductivity responses to fluctuating soil water potential and the capacity to buffer against periods of drought. Yield simulations for the year 2070 were performed under the four representative concentration pathway (RCPs) scenarios presented in the IPCC's 5th Assessment Report. Simulations on low‐grade land suggest that O. ficus‐indica alone has the capacity to meet ‘extreme’ bioenergy demand scenarios (>600 EJ yr^?1) and is highly resilient to climate change (?1%). Agave tequilana is moderately impacted (?11%). These results are significant because bioenergy demand scenarios >600 EJ yr^?1 could be met without significantly increasing conflicts with food production and contributing to deforestation. Both CAM candidates outperformed the C4 bioenergy crop, Panicum virgatum L. (switchgrass) in arid zones in the latitudinal range 30°S–30°N.     

Bio‐mitigation of carbon following afforestation of abandoned salinized farmland

As the global demand for food continues to increase, the displacement of food production by using agricultural land for carbon mitigation, via either carbon sequestration, bioenergy or biofuel is a concern. An alternative approach is to target abandoned salinized farmland for mitigation purposes. Australia, for example, has 17 million ha of farmland that is already or could become saline. At a representative, salinized, low rainfall (350 mm yr^?1) site at Wickepin, Western Australia, we demonstrate that afforestation can mitigate carbon emissions through either providing a feedstock for bioenergy or second generation biofuel production and produce salt‐tolerant fodder for livestock. A range of factors markedly affect this mitigation. These include hydrological conditions such as salinity, site factors such as slope position and soil properties and a range of silvicultural factors such as species, planting density and age of the planting. High density (2000 stems ha^?1) plantings of Eucalyptus occidentalis Endl. produced a mean total biomass of 4.6 t ha^?1 yr^?1 (8.5 t CO₂‐e ha^?1 yr^?1) averaged over 8 years. Atriplex nummularia Lindl. produced a mean total biomass of 3.8 t ha^?1 yr^?1 (6.9 t CO₂‐e ha^?1 yr^?1) averaged over 4 years and approximately 1.9 t ha^?1 yr^?1 of edible dry matter annually to 8 years of age. With differences in salt tolerance between E. occidentalis and A. nummularia, we propose an integrated approach to treating salinized sites that takes salinity gradients into account, replicates natural wetland ecosystems and produces both fodder and biomass. Continued mitigation is expected as the stands mature, assuming that growth is not affected by the accumulation of salt in the soil profile. Such carbon mitigation could potentially be applied to salinized farmland globally, and this could thus represent a major contribution to global carbon mitigation without competing with food production.     

Spatial evaluation of switchgrass productivity under historical and future climate scenarios in Michigan

Switchgrass (Panicum virgatum) productivity on marginal and fertile lands has not been thoroughly evaluated in a systematic manner that includes soil–crop–weather–management interactions and to quantify the risk of failure or success in growing the crop. We used the Systems Approach to Land Use Sustainability (SALUS) model to identify areas with low risk of failing to having more than 8000 kg ha^?1 yr^?1 switchgrass aboveground net primary productivity (ANPP) under rainfed and unfertilized conditions. In addition, we diagnosed constraining factors for switchgrass growth, and tested the effect of nitrogen fertilizer application on plant productivity across Michigan for 30 years under three climate scenarios (baseline climate in 1981–2010, future climate with emissions using RCP 2.6 and RCP 6.0). We determined that <16% of land in Michigan may have at least 8 Mg ha^?1 yr^?1 ANPP under rainfed and unfertilized management with a low risk of failure. Of the productive low‐risk land, about 25% was marginal land, with more than 80% of which was affected by limited water availability due to low soil water‐holding capacity and shallow depth. About 80% of the marginal land was N limited under baseline conditions, but that percentage decreased to 58.5% and 42.1% under RCP 2.6 and RCP 6.0 climate scenarios, respectively, partly due to shorter growing season, smaller plants and less N demand. We also found that the majority of Michigan's land could have high switchgrass ANPP and low risk of failure with no more than 60 kgN ha^?1 fertilizer input. We believe that the methodology used in this study works at different spatial scales, as well as for other biofuel crops.     

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.     

Carbon dioxide exchange dynamics over a mature switchgrass stand

Switchgrass (Panicum virgatum L.) has gained importance as feedstock for bioenergy over the last decades due to its high productivity for up to 20 years, low input requirements, and potential for carbon sequestration. However, data on the dynamics of CO₂ exchange of mature switchgrass stands (>5 years) are limited. The objective of this study was to determine net ecosystem exchange (NEE), ecosystem respiration (Re), and gross primary production (GPP) for a commercially managed switchgrass field in its sixth (2012) and seventh (2013) year in southern Ontario, Canada, using the eddy covariance method. Average NEE flux over two growing seasons (emergence to harvest) was ?10.4 μmol m^?2 s^?1 and reached a maximum uptake of ?42.4 μmol m^?2 s^?1. Total annual NEE was ?380 ± 25 and ?430 ± 30 g C m^?2 in 2012 and 2013, respectively. GPP reached ?1354 ± 23 g C m^?2 in 2012 and ?1430 ± 50g C m^?2 in 2013. Annual Re in 2012 was 974 ± 20 g C m^?2 and 1000 ± 35 g C m^?2 in 2013. GPP during the dry year of 2012 was significantly lower than that during the normal year of 2013, but yield was significantly higher in 2012 with 1090 g  m^?2, compared to 790 g m^?2 in 2013. If considering the carbon removed at harvest, the net ecosystem carbon balance came to 106 ± 45 g C  m^?2 in 2012, indicating a source of carbon, and to ?59 ± 45 g C m^?2 in 2013, indicating a sink of carbon. Our results confirm that switchgrass can switch between being a sink and a source of carbon on an annual basis. More studies are needed which investigate this interannual variability of the carbon budget of mature switchgrass stands.     

Quantifying above‐ and belowground biomass carbon loss with forest conversion in tropical lowlands of Sumatra (Indonesia)

Natural forests in South‐East Asia have been extensively converted into other land‐use systems in the past decades and still show high deforestation rates. Historically, lowland forests have been converted into rubber forests, but more recently, the dominant conversion is into oil palm plantations. While it is expected that the large‐scale conversion has strong effects on the carbon cycle, detailed studies quantifying carbon pools and total net primary production (NPP_total) in above‐ and belowground tree biomass in land‐use systems replacing rainforest (incl. oil palm plantations) are rare so far. We measured above‐ and belowground carbon pools in tree biomass together with NPP_total in natural old‐growth forests, ‘jungle rubber’ agroforests under natural tree cover, and rubber and oil palm monocultures in Sumatra. In total, 32 stands (eight plot replicates per land‐use system) were studied in two different regions. Total tree biomass in the natural forest (mean: 384 Mg ha^?1) was more than two times higher than in jungle rubber stands (147 Mg ha^?1) and >four times higher than in monoculture rubber and oil palm plantations (78 and 50 Mg ha^?1). NPP_total was higher in the natural forest (24 Mg ha^?1 yr^?1) than in the rubber systems (20 and 15 Mg ha^?1 yr^?1), but was highest in the oil palm system (33 Mg ha^?1 yr^?1) due to very high fruit production (15–20 Mg ha^?1 yr^?1). NPP_total was dominated in all systems by aboveground production, but belowground productivity was significantly higher in the natural forest and jungle rubber than in plantations. We conclude that conversion of natural lowland forest into different agricultural systems leads to a strong reduction not only in the biomass carbon pool (up to 166 Mg C ha^?1) but also in carbon sequestration as carbon residence time (i.e. biomass‐C:NPP‐C) was 3–10 times higher in the natural forest than in rubber and oil palm plantations.     

Importance of biophysical effects on climate warming mitigation potential of biofuel crops over the conterminous United States

Current quantification of climate warming mitigation potential (CWMP) of biomass‐derived energy has focused primarily on its biogeochemical effects. This study used site‐level observations of carbon, water, and energy fluxes of biofuel crops to parameterize and evaluate the community land model (CLM) and estimate CO₂ fluxes, surface energy balance, soil carbon dynamics of corn (Zea mays), switchgrass (Panicum virgatum), and miscanthus (Miscanthus × giganteus) ecosystems across the conterminous United States considering different agricultural management practices and land‐use scenarios. We find that neglecting biophysical effects underestimates the CWMP of transitioning from croplands and marginal lands to energy crops. Biogeochemical effects alone result in changes in carbon storage of ?1.9, 49.1, and 69.3 g C m^?2 y^?1 compared to 20.5, 78.5, and 96.2 g C m^?2 y^?1 when considering both biophysical and biogeochemical effects for corn, switchgrass, and miscanthus, respectively. The biophysical contribution to CWMP is dominated by changes in latent heat fluxes. Using the model to optimize growth conditions through fertilization and irrigation increases the CWMP further to 79.6, 98.3, and 118.8 g C m^?2 y^?1, respectively, representing the upper threshold for CWMP. Results also show that the CWMP over marginal lands is lower than that over croplands. This study highlights that neglecting the biophysical effects of altered surface energy and water balance underestimates the CWMP of transitioning to bioenergy crops at regional scales.     

Bioenergy crop productivity and potential climate change mitigation from marginal lands in the United States: An ecosystem modeling perspective

Growing biomass feedstocks from marginal lands is becoming an increasingly attractive choice for producing biofuel as an alternative energy to fossil fuels. Here, we used a biogeochemical model at ecosystem scale to estimate crop productivity and greenhouse gas (GHG) emissions from bioenergy crops grown on marginal lands in the United States. Two broadly tested cellulosic crops, switchgrass, and Miscanthus, were assumed to be grown on the abandoned land and mixed crop‐vegetation land with marginal productivity. Production of biomass and biofuel as well as net carbon exchange and nitrous oxide emissions were estimated in a spatially explicit manner. We found that, cellulosic crops, especially Miscanthus could produce a considerable amount of biomass, and the effective ethanol yield is high on these marginal lands. For every hectare of marginal land, switchgrass and Miscanthus could produce 1.0–2.3 kl and 2.9–6.9 kl ethanol, respectively, depending on nitrogen fertilization rate and biofuel conversion efficiency. Nationally, both crop systems act as net GHG sources. Switchgrass has high global warming intensity (100–390 g CO₂eq l^?1 ethanol), in terms of GHG emissions per unit ethanol produced. Miscanthus, however, emits only 21–36 g CO₂eq to produce every liter of ethanol. To reach the mandated cellulosic ethanol target in the United States, growing Miscanthus on the marginal lands could potentially save land and reduce GHG emissions in comparison to growing switchgrass. However, the ecosystem modeling is still limited by data availability and model deficiencies, further efforts should be made to classify crop‐specific marginal land availability, improve model structure, and better integrate ecosystem modeling into life cycle assessment.     

Using CO2 to enhance carbon capture and biomass applications of freshwater macroalgae

A major limiting factor in the development of algae as a feedstock for the bioenergy industry is the consistent production and supply of biomass. This study is the first to access the suitability of the freshwater macroalgal genus Oedogonium to supply biomass for bioenergy applications. Specifically, we quantified the effect of CO₂ supplementation on the rate of biomass production, carbon capture, and feedstock quality of Oedogonium when cultured in large‐scale outdoor tanks. Oedogonium cultures maintained at a pH of 7.5 through the addition of CO₂ resulted in biomass productivities of 8.33 (±0.51) g DW m^?2 day^?1, which was 2.5 times higher than controls which had an average productivity of 3.37 (±0.75) g DW m^?2 day^?1. Under these productivities, Oedogonium had a carbon content of 41–45% and a higher heating value of 18.5 MJ kg^?1, making it an ideal biomass energy feedstock. The rate of carbon fixation was 1380 g C m^?2 yr^?1 and 1073.1 g C m^?2 yr^?1 for cultures maintained at a pH of 7.5 and 8.5, and 481 g C m^?2 yr^?1 for cultures not supplemented with CO₂. This study highlights the potential of integrating the large‐scale culture of freshwater macroalgae with existing carbon waste streams, for example coal‐fired power stations, both as a tool for carbon sequestration and as an enhanced and sustainable source of bioenergy.     

Bioenergy Crops and Carbon Sequestration

Greenhouse gas (GHG) emissions constitute a global problem. The need for agricultural involvement in GHG mitigation has been widely recognized since the 1990s. The concept of C sinks, C credits, and emission trading has attracted special interests in herbaceous and woody species as energy crops and source of biofuel feedstock. Bioenergy crops are defined as any plant material used to produce bioenergy. These crops have the capacity to produce large volume of biomass, high energy potential, and can be grown in marginal soils. Planting bioenergy crops in degraded soils is one of the promising agricultural options with C sequestration rates ranging from 0.6 to 3.0 Mg C ha^?1 yr^?1. About 60 million hectares (Mha) of land is available in the United States and 757 Mha in the world to grow bioenergy crops. With an energy offset of 1 kg of C in biomass per 0.6 kg of C in fossil fuel, there exists a vast potential of offsetting fossil fuel emission. Bioenergy crops have the potential to sequester approximately 318 Tg C yr^?1 in the United States and 1631 Tg C yr^?1 worldwide. Bioenergy crops consist of herbaceous bunch-type grasses and short-rotation woody perennials. Important grasses include switchgrass (Panicum virgatum L.), elephant grass (Pennissetum purpureum Schum.), tall fescue (Fetusca arundinacea L.), etc. Important among short-rotation woody perennials are poplar (Populus spp.), willow (Salix spp.), mesquite (Prosopis spp.), etc. The emissions of CO₂ from using switchgrass as energy crop is 1.9 kg C Gj^?1 compared with 13.8, 22.3, and 24.6 kg C Gj^?1 from using gas, petroleum, and coal, respectively. Mitigation of GHG emissions cannot be achieved by C sinks alone, a substantial reduction in fossil fuel combustion will be necessary. Carbon sequestration and fossil fuel offset by bioenergy crops is an important component of a possible total societal response to a GHG emission reduction initiative.     

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.     

Soil carbon and belowground carbon balance of a short‐rotation coppice: assessments from three different approaches

Uncertainty in soil carbon (C) fluxes across different land‐use transitions is an issue that needs to be addressed for the further deployment of perennial bioenergy crops. A large‐scale short‐rotation coppice (SRC) site with poplar (Populus) and willow (Salix) was established to examine the land‐use transitions of arable and pasture to bioenergy. Soil C pools, output fluxes of soil CO₂, CH₄, dissolved organic carbon (DOC) and volatile organic compounds, as well as input fluxes from litter fall and from roots, were measured over a 4‐year period, along with environmental parameters. Three approaches were used to estimate changes in the soil C. The largest C pool in the soil was the soil organic carbon (SOC) pool and increased after four years of SRC from 10.9 to 13.9 kg C m^?2. The belowground woody biomass (coarse roots) represented the second largest C pool, followed by the fine roots (Fr). The annual leaf fall represented the largest C input to the soil, followed by weeds and Fr. After the first harvest, we observed a very large C input into the soil from high Fr mortality. The weed inputs decreased as trees grew older and bigger. Soil respiration averaged 568.9 g C m^?2 yr^?1. Leaching of DOC increased over the three years from 7.9 to 14.5 g C m^?2. The pool‐based approach indicated an increase of 3360 g C m^?2 in the SOC pool over the 4‐year period, which was high when compared with the ?27 g C m^?2 estimated by the flux‐based approach and the ?956 g C m^?2 of the combined eddy‐covariance + biometric approach. High uncertainties were associated to the pool‐based approach. Our results suggest using the C flux approach for the assessment of the short‐/medium‐term SOC balance at our site, while SOC pool changes can only be used for long‐term C balance assessments.     

Hydrological responses of land use change from cotton (Gossypium hirsutum L.) to cellulosic bioenergy crops in the Southern High Plains of Texas,USA

The Southern High Plains (SHP) region of Texas in the United States, where cotton is grown in a vast acreage, has the potential to grow cellulosic bioenergy crops such as perennial grasses and biomass sorghum (Sorghum bicolor). Evaluation of hydrological responses and biofuel production potential of hypothetical land use change from cotton (Gossypium hirsutum L.) to cellulosic bioenergy crops enables better understanding of the associated key agroecosystem processes and provides for the feasibility assessment of the targeted land use change in the SHP. The Soil and Water Assessment Tool (SWAT) was used to assess the impacts of replacing cotton with perennial Alamo switchgrass (Panicum virgatum L.), Miscanthus × giganteus (Miscanthus sinensis Anderss. [Poaceae]), big bluestem (Andropogon gerardii) and annual biomass sorghum on water balances, water use efficiency and biofuel production potential in the Double Mountain Fork Brazos watershed. Under perennial grass scenarios, the average (1994–2009) annual surface runoff from the entire watershed decreased by 6–8% relative to the baseline cotton scenario. In contrast, surface runoff increased by about 5% under the biomass sorghum scenario. Perennial grass land use change scenarios suggested an increase in average annual percolation within a range of 3–22% and maintenance of a higher soil water content during August to April compared to the baseline cotton scenario. About 19.1, 11.1, 3.2 and 8.8 Mg ha^?1 of biomass could potentially be produced if cotton area in the watershed would hypothetically be replaced by Miscanthus, switchgrass, big bluestem and biomass sorghum, respectively. Finally, Miscanthus and switchgrass were found to be ideal bioenergy crops for the dryland and irrigated systems, respectively, in the study watershed due to their higher water use efficiency, better water conservation effects, greater biomass and biofuel production potential, and minimum crop management requirements.     

Evaluation of terrestrial carbon cycle models for their response to climate variability and to CO2 trends

The purpose of this study was to evaluate 10 process‐based terrestrial biosphere models that were used for the IPCC fifth Assessment Report. The simulated gross primary productivity (GPP) is compared with flux‐tower‐based estimates by Jung et al. [Journal of Geophysical Research 116 (2011) G00J07] (JU11). The net primary productivity (NPP) apparent sensitivity to climate variability and atmospheric CO₂ trends is diagnosed from each model output, using statistical functions. The temperature sensitivity is compared against ecosystem field warming experiments results. The CO₂ sensitivity of NPP is compared to the results from four Free‐Air CO₂ Enrichment (FACE) experiments. The simulated global net biome productivity (NBP) is compared with the residual land sink (RLS) of the global carbon budget from Friedlingstein et al. [Nature Geoscience 3 (2010) 811] (FR10). We found that models produce a higher GPP (133 ± 15 Pg C yr^?1) than JU11 (118 ± 6 Pg C yr^?1). In response to rising atmospheric CO₂ concentration, modeled NPP increases on average by 16% (5–20%) per 100 ppm, a slightly larger apparent sensitivity of NPP to CO₂ than that measured at the FACE experiment locations (13% per 100 ppm). Global NBP differs markedly among individual models, although the mean value of 2.0 ± 0.8 Pg C yr^?1 is remarkably close to the mean value of RLS (2.1 ± 1.2 Pg C yr^?1). The interannual variability in modeled NBP is significantly correlated with that of RLS for the period 1980–2009. Both model‐to‐model and interannual variation in model GPP is larger than that in model NBP due to the strong coupling causing a positive correlation between ecosystem respiration and GPP in the model. The average linear regression slope of global NBP vs. temperature across the 10 models is ?3.0 ± 1.5 Pg C yr^?1 °C^?1, within the uncertainty of what derived from RLS (?3.9 ± 1.1 Pg C yr^?1 °C^?1). However, 9 of 10 models overestimate the regression slope of NBP vs. precipitation, compared with the slope of the observed RLS vs. precipitation. With most models lacking processes that control GPP and NBP in addition to CO₂ and climate, the agreement between modeled and observation‐based GPP and NBP can be fortuitous. Carbon–nitrogen interactions (only separable in one model) significantly influence the simulated response of carbon cycle to temperature and atmospheric CO₂ concentration, suggesting that nutrients limitations should be included in the next generation of terrestrial biosphere models.