We studied C and N mineralisation patterns from a large number of plant materials (76 samples, covering 37 species and several plant parts), and quantified how these patterns related to biological origin and selected indicators of chemical composition. We determined C and N contents of whole plant material, in water soluble material and in fractions (neutral detergent soluble material, cellulose, hemicellulose and lignin) obtained by stepwise chemical digestion (modified van Soest method). Plant materials were incubated in a sandy soil under standardised conditions (15°C, optimal water content, no N limitation) for 217 days, and CO 2 evolution and soil mineral N contents were monitored regularly. The chemical composition of the plant materials was very diverse, as indicated by total N ranging from 2 to 59 mg N g )1 , (i.e. C/N-ratios between 7 and 227). Few materials were lignified (median lignin ¼ 4% of total C). A large proportion of plant N was found in the neutral detergent soluble (NDS) fraction (average 84%) but less of the plant C (average 46%). Over the entire incubation period, holocellulose C content was the single factor that best explained the variability of C mineralisation (r ¼ )0.73 to )0.82).Overall, lignin C explained only a small proportion of the variability in C mineralisation (r ¼ )0.44 to )0.51), but the higher the lignin content, the narrower the range of cumulative C mineralisation. Initial net N mineralisation rate was most closely correlated (r ¼ 0.76) to water soluble N content of the plant materials, but from Day 22, net N mineralisation was most closely correlated to total plant N and NDS-N contents (r varied between 0.90 and 0.94). The NDS-N content could thus be used to roughly categorise the net N mineralisation patterns into (i) sustained net N immobilisation for several months; (ii) initial net N immobilisation, followed by some re-mineralisation; and (iii) initially rapid and substantial net N mineralisation. Contrary to other studies, we did not find plant residue C/N or lignin/N-ratio to be closely correlated to decomposition and N mineralisation.
For environmental, as well as agronomic reasons, the turnover of carbon (C) and nitrogen (N) from crop residues, catch crops and green manures incorporated into agricultural soils has attracted much attention. It has previously been found that the C and N content in fractions from stepwise chemical digestion of plant materials constitutes an adequate basis for describing a priori the degradability of both C and N in soil. However, the analyses involved are costly and, therefore, unlikely to be used routinely. The aim of the present work was to develop near infrared (NIR) calibrations for C and N fractions governing decomposition dynamics. Within the five Nordic countries, we sampled a uniquely broad-ranged collection representing most of the fresh and mature plant materials that may be incorporated into agricultural soils from temperate regions. The specific objectives of the current study were (1) to produce NIR calibrations with data on C and N in fractions obtained by stepwise chemical digestion (SCD); (2) to validate these calibrations on independent plant samples and (3) to compare the precision and robustness of these broad-based calibrations with calibrations derived from materials within a narrower quality range. According to an internal validation set, plant N, soluble N, cellulose C, holocellulose (hemicellulose + cellulose) C, soluble C and neutral detergent fibre (NDF) dry matter were the parameters best predicted (r 2 = 0.97, 0.95, 0.94, 0.91, 0.90 and 0.94, respectively). However, the calibrations for soluble C and NDF were regarded as unstable, as their validation statistics were substantially poorer than the calibration statistics. The calibrations for all structural N fractions and lignin C were considered poor (r 2 = 0.47-0.70). By comparing our broad-based calibrations for plant N and NDF with similar calibrations for a sample set representing a commercial forage database, it was evident that the broad-based calibrations predicted a narrow-based sample set better than vice versa. For plant N, the residual mean squared error of prediction (RMSEP), when testing the broad-based calibration with the narrow-based validation set, was substantially smaller than the RMSEP obtained when validating the broad-based calibration internally (1.8 vs 2.7 mg N g -1 dry matter). Overall, the calibrations that performed best were those concerning the parameters most strongly influencing C and N mineralisation from plant materials.
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