Effective soil management is critical to achieving climate change mitigation in plant-based renewable energy systems, yet limitations exist in our understanding of dynamic belowground responses to the cultivation of energy crops. To better understand the belowground dynamics following cultivation of a grassland in a high-yielding tropical perennial C4 grass in a zero-tillage production system, changes in soil carbon (C) pools were quantified, modeled, and projected and the chemical composition of the aggregate-protected pool was determined in support of the simulated dynamics. Multiple C pools with different ecosystem functions and turnover increased following cultivation: immediately available microbial substrate (measured as hot water-soluble C) and active C (determined through laboratory incubation) increased by 12 and 30% respectively over time and soil C accumulated significantly in multiple physical fractions. A more rapid and dynamic nature of multiple C pools and transfers between pools existed than is often assumed in belowground models used widely in the field to simulate soil C accumulation. Multiple indicators of fresh roots, including the more easily degraded lignin monomers and root-derived long chain substituted fatty acids, appeared in aggregate-protected pools of cultivated soils over time since planting. This rapid transfer of plant inputs through active and intermediate C pools into mineral-dominated pools is the ultimate outcome required for building soil C stocks. Initial model runs suggested that this is evident, even on a 2-year frame, in transfer rates of 0.485 and 0.890 from active to slow and slow to passive pools respectively. The rapid transfer of fresh root-derived input to stable pool suggests that soil C under zero-tillage management may be resilient to disturbances, such as replanting following a kill-harvest, that would otherwise result in losses from unprotected or readily available pools.
As part of an integrated energy and climate system, biomass production for bioenergy based on the tropical perennial C4 grass energycane can both offset fossil fuels and store soil carbon (C). We measured energycane yields, root biomass, soil C pools, and soil C stocks in a 4 year field trial and modeled C flow from plants to soils in the surface layer of no‐till energycane planted after more than a century of intensive sugarcane agriculture. Aboveground yields ranged from 16.7 to 19.0 Mg C/ha over the 4 year trial. Although total C stocks did not significantly differ in the surface layer (approx. 0–20 cm) during the study, C in free and occluded light fractions decreased, whereas C in the mineral‐rich dense fraction increased over 4 years. Belowground system inputs, estimated from measurements and informed by convergence in the final soil fraction model, were set to 2.5 Mg C ha−1 year−1. With this input value, we estimated that surface soils retained photosynthetically fixed C predominantly within the mineral‐associated organic matter pool for a mean and median transit time of 177 and 110 years, respectively. Although we did not model C flow to deep soil layers (approx. 0–100 cm), observed C accumulation (11.4 Mg C ha−1 year−1) and root growth down to 120 cm suggest that soil processes and resulting C sequestration at the surface are likely to persist deeper into the soil profile. Energycane, as a strong candidate for climate change mitigation and land degradation remediation, showed high biomass yields and allocation of resources to roots, with sequestered soil C expected to persist for over a century.
The efficacy of C4 grasses as feedstocks for liquid fuel production and their climate mitigation potential remain unresolved in the tropics. To identify highly convertible C4 grasses, we measured final fuels and postprocess biomass produced in two laboratory-scale conversion pathways across 12 species and varieties within the Poaceae (grass) family. Total mass, carbon, and energy in final fuels and postprocess biomass were assessed based on field mass and area-based production. Two lignocellulosic processes were investigated: (1) anaerobic digestion (AD) to methane and (2) hot water pretreatment and enzymatic hydrolysis (HWP-EH) to ethanol. We found AD converted lignocellulose to methane more efficiently in terms of carbon and energy compared to ethanol production using HWP-EH, although improvements to and the optimization of each process could change these contrasts. The resulting data provide design limitations for agricultural production and biorefinery systems that regulate these systems as net carbon sources or sinks to the atmosphere. Median carbon recovery in final fuels and postprocess biomass from the studied C4 grasses were ~5 Mg C ha−1 year−1 for both methane and ethanol, while median energy recovery was ~200 MJ ha−1 year−1 for ethanol and ~275 MJ ha−1 year−1 for methane. The highest carbon and energy recovery from lignocellulose was achieved during methane production from a sugarcane hybrid called energycane, with ~10 Mg C ha−1 year−1 and ~450 MJ ha−1 year−1 of carbon and energy recovered, respectively, from fuels and post-process biomass combined. Carbon and energy recovery during ethanol production was also highest for energycane, with ~9 Mg C ha−1 year−1 and ~350 MJ ha−1 year−1 of carbon and energy recovered in fuels and postprocess biomass combined. Although several process streams remain unresolved, agricultural production and conversion of C4 grasses must operate within these carbon and energy limitations for biofuel and bioenergy production to be an atmospheric carbon sink.