scholarly journals The Development of Theory on Humus and Soil Organic Matter: from Turin and Waksman to Present Days

2017 ◽  
pp. 3-38 ◽  
Author(s):  
A. L. Ivanov ◽  
B. M. Kogut ◽  
V. M. Semenov ◽  
M. . Turina Oberlander ◽  
N. . Waksman Schanbacher

He special merits of Z.A. Waksman and I.V. Turin are marked in the development of soil humus and organic matter theory. Little-known pages ex vivo of these outstanding experimentalist scientists, founders of two schools and acknowledged leaders in the investigation of the soil organic matter, are presented in the article. A comparative analysis of theories by I.V. Turin and Z.A. Waksman on the origins, composition and properties of the soil organic matter is given. Actual conceptions, ways and methods of the organic matter fractioning are described in the work. The alternative points of view on the humine matters of soils by I. V. Turin and Z. A. Waksman are considered. A brief review on the heteropolymeric and supramolecular models of soil humic matter composition is presented.

2019 ◽  
Vol 85 (10) ◽  
Author(s):  
Tao Wang ◽  
Zhaomo Tian ◽  
Anders Tunlid ◽  
Per Persson

ABSTRACT The interactions between dissolved organic matter (DOM) and mineral particles are critical for the stabilization of soil organic matter (SOM) in terrestrial ecosystems. The processing of DOM by ectomycorrhizal fungi contributes to the formation of mineral-stabilized SOM by two contrasting pathways: the extracellular transformation of DOM (ex vivo pathway) and the secretion of mineral-surface-reactive metabolites (in vivo pathway). In this study, we examined how changes in nitrogen (N) availability affected the formation of mineral-associated carbon (C) from these two pathways. DOM was extracted from forest soils. The processing of this DOM by the ectomycorrhizal fungus Paxillus involutus was examined in laboratory-scale studies with different levels of ammonium. At low levels of ammonium (i.e., under N-limited conditions), the DOM components were slightly oxidized, and fungal C metabolites with iron-reducing activity were secreted. Ammonium amendments decreased the amount of C metabolites, and no additional oxidation of the organic matter was detected. In contrast, the hydrolytic activity and the secretion of N-containing compounds increased, particularly when high levels of ammonium were added. Under these conditions, C, but not N, limited fungal growth. Although the overall production of mineral-associated organic C was not affected by ammonium concentrations, the observed shifts in the activities of the ex vivo and in vivo pathways affected the composition of organic matter adsorbed onto the mineral particles. Such changes will affect the properties of organic matter-mineral associations and, thus, ultimately, the stabilization of SOM. IMPORTANCE Nitrogen (N) availability plays a critical role in the cycling and storage of soil organic matter (SOM). However, large uncertainties remain in predicting the net effect of N addition on soil organic carbon (C) storage due to the complex interactions between organic matter, microbial activity, and mineral particles that determine the formation of stable SOM. Here, we attempted to disentangle the effects of ammonium on these interactions in controlled microcosm experiments including the ectomycorrhizal fungus P.involutus and dissolved organic matter extracted from forest soils. Increased ammonium levels affected the fungal processing of the organic material as well as the secretion of extracellular metabolites. Although ammonium additions did not increase the net production of mineral-adsorbed C, changes in the decomposition and secretion pathways altered the composition of the adsorbed organic matter. These changes may influence the properties of the organic matter-mineral associations and, thus, the stabilization of SOM.


1924 ◽  
Vol 14 (3) ◽  
pp. 469-472 ◽  
Author(s):  
T. Eden

Odén has shown that colour intensity comparisons between alkali extracts of peat soils of varying origin can be made since, despite the possible difference in the nature of their humic matter, the absorption spectra are almost identical within the visible range. These absorption spectra are also comparable with that of Merck's Acidum Huminicum, which is a standard preparation. Odén developed his colorimetric method as a means of measuring the degree of humification of the organic matter of peat soils, that is to say, the proportion of the total organic matter which could be classed as humic matter. In this way the disadvantages of Grandeau's method, in which there is no discrimination between the coloured and the colourless parts of the soil organic matter, are obviated.


1987 ◽  
Vol 1 (1) ◽  
pp. 41-45 ◽  
Author(s):  
Jerome B. Weber ◽  
M. Ray Tucker ◽  
Robert A. Isaac

Percent soil organic matter content, as determined by standard chromic acid oxidations, was highly (r = 0.89) correlated with soil humic matter content, as determined by NaOH/DTPA (diethylenetriaminepenta-acetic acid)/alcohol extraction of 201 U.S. soils. Humic matter content of the soils was equally or better correlated (r = 0.89 to 0.97) with herbicide bioactivity, as measured in field experiments, than was percent organic matter content (r = 0.87 to 0.92). Regression equations provided allow herbicide rate recommendations for 80% weed control to be calculated based on soil humic matter or soil organic matter levels.


2021 ◽  
Vol 4 (4) ◽  
Author(s):  
T. V. Alekseeva

The main part of soil organic matter (OM) is mineral-associated: 88 ± 11% of С and even more – 93 ± 9% of N. The aims of the given study were: 1 – to demonstrate experimentally the adsorption selectivity of organic compounds towards minerals with different physico-chemical properties (palygorskite vs montmorillonite); 2 – to characterize mineral-associated OM of buried Late Holocene palaeosols and estimate its diagenetic transformations; 3 – to investigate the OM of humin from modern soils of different genesis and Pleistocene and Holocene palaeosols and estimate its diagenetic transformations. The basic soil properties were determined using standard methods. Clay fractions (<2 um) – natural organo-mineral complexes (OMC) were obtained by sedimentation, their mineralogy was studied by XRD. The elemental composition of OM was studied with CNS-analyzer. The structural characteristics of organic matter were determined with the solid-state 13C-NMR-spectroscopy and FTIR-spectroscopy, isotopic composition of C and N – by mass-spectrometry. The obtained results show that the characteristics of mineral-associated OM depends on the properties of mineral “filter” as well as the fate of OM under diagenesis: how long, in what quantity and quality it will persist. It was shown that palygorskite adsorbed predominantly O-alkyls, which are chemically strongly bound. As a result, the age of fulvic type humus in palygoskite palaeosols can reach 300 My. From other side humus of smectitic paleosols of the same age is present by deeply transformed aromatic structures (“coal”). Mineral-associated OM of buried under kurgans Holocene palaeosols contains more alkyls and carboxylic groups, is less aromatic in a comparison with OM of the respective soils. The specific feature of mineral-associated OM is its enrichment in N-compounds. The later are present by both vegetal and microbial compounds, and demonstrate the large affinity towards the mineral surfaces. The formation of chemical bounds between them provides the persistence of OM in OMC. E.g. H2O2 treatment results in preferential destruction of C-rich compounds and oxidized OM demonstrates larger C/N values. Mineral-associated OM of buried Holocene soils keeps the decreased values of C/N (7–14 vs 14–21 for OM of whole soils). Additionally they are characterized by heavier isotopic composition of δ15N in a comparison with the respective soils (5–11‰ vs 6–9‰). It could be explained either by the accumulation of microbial N, or increasing of the humification degree – the loss of aliphatic C and increasing of aromaticity. Humin is the considerable part of soil humus. Experimentally shown that OM of humins both of soils and OMC is enriched in O-alkyls and C of acetal groups. OM of humins are not homogeneous, and consists from at least two groups: mineral-associated OM and partly mineralized plant fragments. As a consequence, the content of humin in OMC is smaller in a comparison with respective soils. It is concluded that mineral-associated OM and humin as well as soil humus represent dynamic soil systems.


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