The accumulation of carbon (C) and nitrogen (N) was measured on two sites on Rothamsted Farm that had been fenced off some 120 years ago and allowed to revert naturally to woodland. The sites had previously been arable for centuries. One had been chalked and was still calcareous; the other had never been chalked and the pH fell from 7.1 in 1883 to 4.4 in 1999. The acidic site (Geescroft wilderness) is now a deciduous wood, dominated by oak (Quercus robor); the calcareous site (Broadbalk wilderness) is now dominated by ash (Fraxinus excelsior), with sycamore (Acer pseudoplatanus) and hawthorn (Craetagus monogyna) as major contributors. The acidic site gained 2.00 t C ha−1 yr−1 over the 118‐year period (0.38 t in litter and soil to a depth of 69 cm, plus an estimated 1.62 t in trees and their roots); the corresponding gains of N were 22.2 kg N ha−1 year−1 (15.2 kg in the soil, plus 6.9 kg in trees and their roots). The calcareous site gained 3.39 t C ha−1 year−1 over the 120‐year period (0.54 t in the soil, plus an estimated 2.85 t in trees and roots); for N the gains were 49.6 kg ha−1 yr−1 (36.8 kg in the soil, plus 12.8 kg in trees and roots). Trees have not been allowed to grow on an adjacent part of the calcareous site. There is now a little more C and N in the soil from this part than in the corresponding soil under woodland. We argue from our results that N was the primary factor limiting plant growth and hence accumulation of C during the early stages of regeneration in these woodlands. As soil organic N accumulates and the sites move towards N saturation, other factors become limiting. Per unit area of woodland, narrow strips; that is, wide hedges with trees, are the most efficient way of sequestering C – provided that they are not short of N.
Processes that produce only ethanol from lignocellulosics display poor economics. This is generally overcome by constructing large facilities having satisfactory economies of scale, thus making financing onerous and hindering the development of suitable technologies. Lignol Innovations has developed a biorefining technology that employs an ethanol-based organosolv step to separate lignin, hemicellulose components, and extractives from the cellulosic fraction of woody biomass. The resultant cellulosic fraction is highly susceptible to enzymatic hydrolysis, generating very high yields of glucose (>90% in 12-24 h) with typical enzyme loadings of 10-20 FPU (filter paper units)/g. This glucose is readily converted to ethanol, or possibly other sugar platform chemicals, either by sequential or simultaneous saccharification and fermentation. The liquor from the organosolv step is processed by well-established unit operations to recover lignin, furfural, xylose, acetic acid, and a lipophylic extractives fraction. The process ethanol is recovered and recycled back to the process. The resulting recycled process water is of a very high quality, low BOD5, and suitable for overall system process closure. Significant benefits can be attained in greenhouse gas (GHG) emission reductions, as per the Kyoto Protocol. Revenues from the multiple products, particularly the lignin, ethanol and xylose fractions, ensure excellent economics for the process even in plants as small as 100 mtpd (metric tonnes per day) dry woody biomass input a scale suitable for processing wood residues produced by a single large sawmill.
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