scholarly journals Chemical structure peculiarities of different organic matter pools in Haplic Chernozem of the Streleskaya steppe

Author(s):  
N.N. Danchenko ◽  
Z.S. Artemyeva ◽  
Yu.G. Kolyagin ◽  
B.M. Kogut
Author(s):  
Rossana Del Vecchio ◽  
Neil V Blough ◽  
Carmen Cartisano ◽  
Marla Bianca ◽  
Tara M Schendorf ◽  
...  

2021 ◽  
Vol 54 (6) ◽  
pp. 852-864
Author(s):  
Z. S. Artemyeva ◽  
N. N. Danchenko ◽  
E. P. Zazovskaya ◽  
Yu. G. Kolyagin ◽  
N. P. Kirillova ◽  
...  

Forests ◽  
2019 ◽  
Vol 10 (10) ◽  
pp. 914
Author(s):  
Jing Geng ◽  
Shulan Cheng ◽  
Huajun Fang ◽  
Jie Pei ◽  
Meng Xu ◽  
...  

Key Findings: Combining physical fractionation and pyrolysis–gas chromatography/mass spectrometry (py-GC/MS) technique can help better understand the dynamics of soil organic matter (SOM). Background and Objectives: SOM plays a critical role in the global carbon (C) cycle. However, its complexity remains a challenge in characterizing chemical molecular composition within SOM and under nitrogen (N) deposition. Materials and Methods: Three particulate organic matter (POM) fractions within SOM and under N treatments were studied from perspectives of distributions, C contents and chemical signatures in a subtropical forest. N addition experiment was conducted with two inorganic N forms (NH4Cl and NaNO3) applied at three rates of 0, 40, 120 kg N ha−1 yr−1. Three particle-size fractions (>250 μm, 53–250 μm and <53 μm) were separated by a wet-sieving method. Py-GC/MS technique was used to differentiate between chemical composition. Results: A progressive proportion transfer of mineral-associated organic matter (MAOM) to fine POM under N treatment was found. Only C content in fine POM was sensitive to N addition. Principal component analyses (PCA) showed that the coarse POM had the largest plant-derived markers (lignins, phenols, long-chain n-alkanes, and n-alkenes). Short-chain n-alkanes and n-alkenes, benzofurans, aromatics and polycyclic aromatic hydrocarbons mainly from black carbon prevailed in the fine POM. N compounds and polysaccharides from microbial products dominated in the MAOM. Factor analysis revealed that the degradation extent of three fractions was largely distinct. The difference in chemical structure among three particulate fractions within SOM was larger than treatments between control and N addition. In terms of N treatment impact, the MAOM fraction had fewer benzofurans compounds and was enriched in polysaccharides, indicating comparatively weaker mineralization and stronger stabilization of these substances. Conclusions: Our findings highlight the importance of chemical structure in SOM pools and help to understand the influence of N deposition on SOM transformation.


1998 ◽  
Vol 38 (7) ◽  
pp. 667 ◽  
Author(s):  
J. O. Skjemstad ◽  
L. J. Janik ◽  
J. A. Taylor

Summary. Non-living soil organic matter is a small but critical component of soils contributing to soil structure, fertility and a range of other chemical, physical and biological functions. Although considerable work has contributed to our knowledge of its distribution, chemical structure, mineral associations and turnover, there is still little information on which fractions or pools of non-living soil organic matter are implicated in various soil functions and to what extent. This review paper summarises some of what is known about the distribution, chemistry, mineral associations and soil structure, turnover and the measurement of non-living soil organic matter, with particular emphasis on Australia. It also discusses some of the difficulties in using current methods for describing the function of this material in soil.


Soil Research ◽  
2010 ◽  
Vol 48 (8) ◽  
pp. 693 ◽  
Author(s):  
Eben S. Quill ◽  
Michael J. Angove ◽  
David W. Morton ◽  
Bruce B. Johnson

This study investigated the chemical structure of extracted dissolved organic matter (DOM) derived from thermally altered plant material found in the box–ironbark environments of central Victoria, namely: Eucalyptus tricarpa, Pinus pinaceae, Isolepsis nodosa, Acacia pycnantha, and Cassinia arcuata. Samples taken from the plants were burnt at 150, 300, and 400°C, under oxidising and reducing conditions in order to represent the variable combustion undergone by plants during bushfire events. The extraction of DOM from the burnt residues into water was conducted over 96 h. During the extraction period, solution concentrations of DOM were measured using HPLC and TOC methods, while the chemistry of the extracted DOM was characterised using ATR-IR. The nature of the extracted DOM depended on the originating species and whether burnt under oxidising or reducing conditions. DOM derived from the residues of the Australian native trees and shrubs (E. tricarpa, A. pycnantha, and C. arcuata) were generally more aromatic and conjugated than the materials extracted from herbaceous I. nodosa and introduced dendrophyte P. pinaceae. When burnt under reducing conditions, fire residues were less polar, indicated by the fact that they were significantly less soluble and ATR-IR spectra spectroscopy showed little OH stretching compared with the extracts obtained under oxidising conditions. Water extracts from the burnt residues sorbed strongly to the mineral goethite, but had less affinity for the kaolinite surface.


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