scholarly journals Stability of soil aggregates and their ability of carbon sequestration

2014 ◽  
Vol 9 (No. 3) ◽  
pp. 111-118 ◽  
Author(s):  
V. Šimanský ◽  
D. Bajčan
Keyword(s):  
Organic Matter ◽  
Carbon Sequestration ◽  
Soil Organic Matter ◽  
Soil Aggregates ◽  
Size Fraction ◽  
Size Fractions ◽  
Water Stable Aggregates ◽  
Binding Agents ◽  
Carbon Reservoir ◽  
The Stability

One of the most important binding agents for forming stable aggregates is a soil organic matter (SOM), which can be retained in various size fractions of aggregates. If aggregates are water-resistant, they retain more carbon. Therefore, the aim of this study was to evaluate the stability of aggregates and their ability of carbon sequestration in different soil types and soil management systems in Slovakian vineyards. The highest content of water-stable macro-aggregates (WSA<sub>ma</sub>) was determined in Cambisols, and the lowest in Fluvisols. The highest content of WSA<sub>ma</sub> (size fraction 0.5&ndash;3 mm) was determined in Chernozems, decreasing within the following sequence: Fluvisols &gt; Leptosols &gt; Cambisols &gt; Luvisols. The soil type had a statistically significant influence on the re-distribution of soil organic matter in size fractions of water-stable aggregates. The highest content of SOM in water-stable aggregates of the vineyards was determined in grassy strips in-between the vineyard rows in comparison to intensively cultivated rows of vineyard. The highest values of carbon sequestration capacity (CSC) in WSA<sub>ma</sub> were found in Cambisols &gt; Leptosols and the lowest values of CSC were in Fluvisols. The micro-aggregates represented a significant carbon reservoir for the intensively cultivated soils (rows of vineyard). On the other hand, increasing of macro-aggregates (size fraction 0.5&ndash;3 mm) was characteristic for grassland soils (between the rows of vineyard).

Free soil colloids and colloidal building units of soil aggregates

2020 ◽  
Author(s):  
Ni Tang ◽  
Nina Siebers ◽  
Erwin Klumpp
Keyword(s):  
Mass Spectrometry ◽  
Organic Matter ◽  
Organic Carbon ◽  
Inductively Coupled Plasma ◽  
Soil Aggregates ◽  
Size Fraction ◽  
Ionization Mass ◽  
Soil Matrix ◽  
Size Fractions ◽  
20 Nm

&lt;p&gt;Nanosized mineral particles and organic matter (&lt;100 nm) ,as well as their associations, belong to the most important ingredients for the formation of the soil aggregate structure being a hierarchically organized system. Colloids (&lt; 220 nm) including nanoparticles can be occluded as primary building units of soil aggregates. Nevertheless, a large proportion of these colloids is mobile and presents in the solution phase (as &amp;#8220;free&amp;#8221;) within the soil matrix. However, the differences between &amp;#8220;free&amp;#8221; and occluded colloids remain unclear.&lt;/p&gt;&lt;p&gt;Here, both occluded and free colloids were isolated from soil samples of an arable field with different clay contents (19% and 34%) using wet sieving and centrifugation. The release of occluded colloids from soil macroaggregates (&gt;250 &amp;#181;m) was carried out with ultrasonic treatment at 1000 J mL&lt;sup&gt;-1&lt;/sup&gt;. The free and occluded colloidal fractions were then characterized for their size-resolved elemental composition using flow field-flow fractionation inductively coupled plasma mass spectrometry and organic carbon detector (FFF-ICP-MS/OCD). In addition, selected samples were also subjected to transmission electron microscopy as well as pyrolysis field ionization mass spectrometry (Py-FIMS).&lt;/p&gt;&lt;p&gt;Both, free and occluded colloids were composed of three size fractions: nanoparticles &lt;20 nm, medium-sized nanoparticles (20 nm&amp;#8211;60 nm), and, fine colloids (60 nm&amp;#8211;220 nm). The fine colloid fraction was the dominant size fraction in both free and occluded colloids, which mainly consist of organic carbon, Al, Si, and Fe, probably present as phyllosilicates and associations of Fe- and Al- (hydr)oxides and organic matter. However, the organic matter contents for all three size fractions were higher for the occluded colloids than for the free ones. The role of OM concentration and composition in these colloids will be discussed in the paper.&lt;/p&gt;

ÉTUDE COMPARATIVE DE L'AGRÉGATION ET DE LA MATIÈRE ORGANIQUE ASSOCIÉE AUX FRACTIONS GRANULOMÉTRIQUES DE SEPT SOLS SOUS CULTURE DE MAÏS OU EN PRAIRIE

1990 ◽  
Vol 70 (3) ◽  
pp. 395-402 ◽  
Author(s):  
J. ELUSTONDO ◽  
M. R. LAVERDIÈRE ◽  
D. A. ANGERS ◽  
A. N'DAYEGAMIYE
Keyword(s):  
Particle Size ◽  
Organic Matter ◽  
Size Fraction ◽  
Cropping System ◽  
Clay Content ◽  
Size Fractions ◽  
Particle Size Fractions ◽  
Carbon And Nitrogen ◽  
Water Stable Aggregates ◽  
Continuous Corn

Water-stable aggregation and organic matter associated with particle-size fractions were compared for seven pairs of soils that were either under meadow or continuous corn cropping for more than 5 yr. Soils that have remained under meadow contained 25 and 29% more carbon and nitrogen than those under continuous corn. Carbon contents of the sand- and silt-size fractions were also 61 and 15% higher, respectively, under meadow than under continuous corn. The cropping system had no significant effect on the carbon and nitrogen contents of the clay-size fractions. The amount of water-stable aggregates (> 1 mm) was on average 34% higher in soils under meadow than in soils under corn cropping. Significant correlations were found between water-stable aggregates and total C (r = 0.77) and C in sand-size fraction (r = 0.79). The results also indicate that the beneficial effect of meadow over continuous corn on soil aggregation increases as soil clay content increases. Key words: Aggregation, organic matter, particle-size fractions, corn, meadow

Structural Characterization of Soil Organic Matter and Humic Acids in Particle-Size Fractions of an Agricultural Soil

2002 ◽  
Vol 66 (1) ◽  
pp. 129 ◽  
Author(s):  
Benny Chefetz ◽  
Jorge Tarchitzky ◽  
Ashish P. Deshmukh ◽  
Patrick G. Hatcher ◽  
Yona Chen
Keyword(s):  
Particle Size ◽  
Organic Matter ◽  
Soil Organic Matter ◽  
Humic Acids ◽  
Structural Characterization ◽  
Agricultural Soil ◽  
Size Fractions ◽  
Particle Size Fractions

scholarly journals Long term trends in fertility of soils under continuous cultivation and cereal cropping in southern Queensland. III. Distribution and kinetics of soil organic carbon in particle size fractions

Soil Research ◽  
1986 ◽  
Vol 24 (2) ◽  
pp. 293 ◽  
Author(s):  
RC Dalal ◽  
RJ Mayer
Keyword(s):  
Particle Size ◽  
Organic Matter ◽  
Organic Carbon ◽  
Soil Organic Carbon ◽  
Size Fraction ◽  
Organic C ◽  
Size Fractions ◽  
Particle Size Fractions ◽  
Clay Size Fraction ◽  
Sand Size

Distribution of soil organic carbon in sand-, silt- and clay-size fractions during cultivation for periods ranging from 20 to 70 years was studied in six major soils used for cereal cropping in southern Queensland. Particle-size fractions were obtained by dispersion in water using cation exchange resin, sieving and sedimentation. In the soils' virgin state no single particle-size fraction was found to be consistently enriched as compared to the whole soil in organic C in all six soils, although the largest proportion (48%) of organic C was in the clay-size fraction; silt and sand-size fractions contained remaining organic C in equal amounts. Upon cultivation, the amounts of organic C declined from all particle-size fractions in most soils, although the loss rates differed considerably among different fractions and from the whole soil. The proportion of the sand-size fraction declined rapidly (from 26% to 12% overall), whereas that of the clay-size fraction increased from 48% to 61% overall. The proportion of silt-size organic C was least affected by cultivation in most soils. It was inferred, therefore, that the sand-size organic matter is rapidly lost from soil, through mineralization as well as disintegration into silt-size and clay-size fractions, and that the clay fraction provides protection for the soil organic matter against microbial and enzymic degradation.

scholarly journals Droplet infiltration dynamics and soil wettability related to soil organic matter of soil aggregate coatings and interiors

2016 ◽  
Vol 64 (2) ◽  
pp. 111-120 ◽  
Author(s):  
Miroslav Fér ◽  
Martin Leue ◽  
Radka Kodešová ◽  
Horst H. Gerke ◽  
Ruth H. Ellerbrock
Keyword(s):  
Organic Matter ◽  
Soil Organic Matter ◽  
Preferential Flow ◽  
Water Drop ◽  
Soil Aggregates ◽  
High Water ◽  
Contact Angles ◽  
Surface Wettability ◽  
Mineral Coatings ◽  
Droplet Infiltration

Abstract The organo-mineral coatings of soil aggregates, cracks, and biopores control sorption and macropore-matrix exchange during preferential flow, in particular in the clay-illuvial Bt-horizon of Luvisols. The soil organic matter (SOM) composition has been hypothesized to explain temporal changes in the hydraulic properties of aggregate surfaces. The objective of this research was to find relations between the temporal change in wettability, in terms of droplet infiltration dynamics, and the SOM composition of coated and uncoated aggregate surfaces. We used 20 to 40 mm sized soil aggregates from the Bt2 horizon of a Haplic Luvisol from loess that were (i) coated, (ii) not coated (both intact), and (iii) aggregates from which coatings were removed (cut). The SOM composition of the aggregate surfaces was characterized by infrared spectroscopy in the diffuse reflection mode (DRIFT). A potential wettability index (PWI) was calculated from the ratio of hydrophobic and hydrophilic functional groups in SOM. The water drop penetration times (WDPT) and contact angles (CA) during droplet infiltration experiments were determined on dry and moist aggregate samples of the three types. The decrease in the CA with time was described using the power function (CA(t) = at−b). For dry aggregates, the WDPT values were larger for coated as compared to uncoated regions on the aggregate surfaces, and increased with increasing PWI value (R2 = 0.75). The a parameter was significantly related to the WDPT (R2 = 0.84) and to the PWI (R2 = 0.64). The relations between the b parameter and the WDPT (R2 = 0.61) and the PWI (R2 = 0.53) were also significant. The WDPT values of wet soil aggregates were higher than those of dry aggregates due to high water contents, which limited the droplet infiltration potential. At the wet aggregate surfaces, the WDPT values increased with the PWI of the SOM (R2 = 0.64). In contrast to dry samples, no significant relationships were found between parameters a or b of CA(t) and WDPT or PWI for wet aggregate surfaces. The results suggest that the effect of the SOM composition of coatings on surface wettability decreases with increasing soil moisture. In addition to the dominant impact of SOM, the wettability of aggregate surfaces could be affected by different mineralogical compositions of clay in coatings and interiors of aggregates. Particularly, wettability of coatings could be decreased by illite which was the dominant clay type in coatings. However, the influence of different clay mineral fractions on surface wettability was not due to small number of measurements (2 and 1 samples from coatings and interiors, respectively) quantified.

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