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首页> 外文期刊>Ecosystems >Chemical Changes During 6 Years of Decomposition of 11 Litters in Some Canadian Forest Sites. Part 2. p#pdC Abundance, Solid-State p#pdC NMR Spectroscopy and the Meaning of Lignin
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Chemical Changes During 6 Years of Decomposition of 11 Litters in Some Canadian Forest Sites. Part 2. p#pdC Abundance, Solid-State p#pdC NMR Spectroscopy and the Meaning of Lignin

机译:在加拿大某些森林站点分解11种垃圾的6年中,化学变化。第2部分。p#pdC丰度,固态p#pdC NMR光谱学和木质素的含义

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There is still a poor understanding of how changes in the organic composition of litter contribute to slowing or even cessation of decomposition. Using p#pdC nuclear magnetic resonance (NMR) spectroscopy of samples from the Canadian Intersite Decomposition Experiment (CIDET), we asked whether increasing lignin per se could account for the well-known increase in acid-unhydrolyzable residue (AUR), and secondly, using three litters from four sites with different mean annual temperatures, whether changes in organic composition would follow similar trajectories with C mass loss. At 6 years, there was 16-39% C remaining for 10 foliar litters and wood blocks at a site with rapid initial decomposition, and higher amounts remaining for three species at three colder sites. p#pdC NMR spectra obtained with rapid cross-polarization (CP) mainly showed increasing similarity among the foliar litters, although wood showed little change in composition. Foliage generally showed loss of O- and di-O-alkyl C, mainly from carbohydrate, and increase in alkyl, aromatic, phenolic and carboxyl C. However, O-alkyl C loss was limited, especially for litters with slow initial decomposition, and many litters showed relatively small changes in intensity distribution. Quantitative p#pdC (BD) spectra showed similar trends, but even smaller changes in C composition, and 6-year CP difference spectra showed that C was lost across the whole range of structures. Changes in tp#pdC were small and variable, but could be correlated to some extent with loss of carbohydrates versus tannins. Lignin was not selectively preserved, and the increase of resistant structures derived from lignin, tannins, and cutin collectively accounts for increasing AUR. Compositional changes of NMR C fractions across sites with different temperatures were small and inconsistent, likely due to the influence of other site factors; however, changes in their contents did largely follow consistent trajectories with %C remaining.
机译:对于垃圾的有机成分的变化如何导致减缓甚至停止分解的认识仍然很差。使用来自加拿大现场分解实验(CIDET)的样品的p#pdC核磁共振(NMR)光谱,我们询问木质素本身的增加是否可以解释众所周知的酸不可水解残基(AUR)的增加,其次,使用来自四个地点的年平均温度不同的三个垫料,有机组成的变化是否会遵循相似的轨迹,且质量损失为C。在6年时,在迅速分解初期的10个叶凋落物和木块中,仍有16-39%的C残留,而在三个较冷的地点,三个物种的残留量更高。尽管木材的组成几乎没有变化,但通过快速交叉极化(CP)获得的p#pdC NMR光谱主要显示出叶凋落物之间的相似性不断提高。叶子通常表现出主要由碳水化合物引起的O-和二-O-烷基C的损失,以及烷基,芳族,酚和羧基C的增加。但是,O-烷基C的损失是有限的,特别是对于初期分解较慢的垃圾而言。许多垃圾的强度分布变化较小。定量p#pdC(BD)光谱显示出相似的趋势,但C组成的变化更小,并且6年CP差异光谱显示C在整个结构范围内都丢失了。 tp#pdC的变化很小且变化不定,但在一定程度上可能与碳水化合物相对单宁的损失有关。木质素未被选择性地保存,并且源自木质素,单宁和角质的抗性结构的增加共同导致了AUR的增加。跨温度不同的站点的NMR C馏分的组成变化很小且不一致,可能是由于其他站点因素的影响。但是,其内容的变化确实遵循了一致的轨迹,且剩余%C。

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