Abstract

AbstractConversion of large areas of agricultural grassland is inevitable if European and UK domestic production of biomass is to play a significant role in meeting demand. Understanding the impact of these land‐use changes on soil carbon cycling and stocks depends on accurate predictions from well‐parameterized models. Key considerations are cultivation disturbance and the effect of autotrophic root input stimulation on soil carbon decomposition under novel biomass crops. This study presents partitioned parameters from the conversion of semi‐improved grassland to Miscanthus bioenergy production and compares the contribution of autotrophic and heterotrophic respiration to overall ecosystem respiration of CO2 in the first and second years of establishment. Repeated measures of respiration from within and without root exclusion collars were used to produce time‐series model integrations separating live root inputs from decomposition of grass residues ploughed in with cultivation of the new crop. These parameters were then compared to total ecosystem respiration derived from eddy covariance sensors. Average soil surface respiration was 13.4% higher in the second growing season, increasing from 2.9 to 3.29 g CO2‐C m−2 day−1. Total ecosystem respiration followed a similar trend, increasing from 4.07 to 5.4 g CO2‐C m−2 day−1. Heterotrophic respiration from the root exclusion collars was 32.2% lower in the second growing season at 1.20 g CO2‐C m−2 day−1 compared to the previous year at 1.77 g CO2‐C m−2 day−1. Of the total respiration flux over the two‐year time period, aboveground autotrophic respiration plus litter decomposition contributed 38.46% to total ecosystem respiration while belowground autotrophic respiration and stimulation by live root inputs contributed 46.44% to soil surface respiration. This figure is notably higher than mean figures for nonforest soils derived from the literature and demonstrates the importance of crop‐specific parameterization of respiration models.

Highlights

  • IntroductionThe stay-green trait has been used for years by breeders as a measure of post-flowering drought tolerance (Rosenow and Clark, 1981; Borrell et al, 2001) and is a mechanism that prevents premature senescence under

  • The mean number of alleles was highest in SBI-10 (8.3) followed by SBI-09 and SBI-06 (7), SBI-01 and SBI-04 (6.8), SBI-02 (6.6) SBI-08 (6.4) SBI-07 (5.5), SBI-03 (5.3) and SBI-05 with the least (3.7)

  • Derivatives of B35, KS19 and E36-1 clustered together with their parental lines based on all 68 simple sequence repeats (SSR), while IS3620C was the least related with any other genotype

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Summary

Introduction

The stay-green trait has been used for years by breeders as a measure of post-flowering drought tolerance (Rosenow and Clark, 1981; Borrell et al, 2001) and is a mechanism that prevents premature senescence under. Understanding the inheritance of traits, such as stay-green, is important for its successful application in plant breeding programmes. Alleles of simple sequence repeats (SSR) associated with stay-green quantitative trait loci (QTL) have been identified in a number of genetic sources (Borrell et al, 2000ab; Bhattramakki et al, 2000; Kebede et al, 2001; Kong et al, 2000; Haussmann et al, 2002), which might influence their tolerance on post-flowering drought stress. Different genetic sources of stay-green may employ different genes and display different inheritance characteristics

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