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

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...

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Veröffentlicht in:Journal of Hydrology and Hydromechanics 2016-06, Vol.64 (2), p.111-120
Hauptverfasser: Fér, Miroslav, Leue, Martin, Kodešová, Radka, Gerke, Horst H., Ellerbrock, Ruth H.
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container_issue 2
container_start_page 111
container_title Journal of Hydrology and Hydromechanics
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creator Fér, Miroslav
Leue, Martin
Kodešová, Radka
Gerke, Horst H.
Ellerbrock, Ruth H.
description 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 ( R 2 = 0.75). The a parameter was significantly related to the WDPT ( R 2 = 0.84) and to the PWI ( R 2 = 0.64). The relations between the b parameter and the WDPT ( R 2 = 0.61) and the PWI ( R 2 = 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 ( R 2 = 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
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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 ( R 2 = 0.75). The a parameter was significantly related to the WDPT ( R 2 = 0.84) and to the PWI ( R 2 = 0.64). The relations between the b parameter and the WDPT ( R 2 = 0.61) and the PWI ( R 2 = 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 ( R 2 = 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. 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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 ( R 2 = 0.75). The a parameter was significantly related to the WDPT ( R 2 = 0.84) and to the PWI ( R 2 = 0.64). The relations between the b parameter and the WDPT ( R 2 = 0.61) and the PWI ( R 2 = 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 ( R 2 = 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.</abstract><cop>Bratislava</cop><pub>De Gruyter Poland</pub><doi>10.1515/johh-2016-0021</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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source De Gruyter Open Access Journals; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Aggregates
clay and organic matter coatings
Contact angle
drift spectroscopy
Mineralogy
Soil sciences
Spectrum analysis
wdpt
Worms
title Droplet infiltration dynamics and soil wettability related to soil organic matter of soil aggregate coatings and interiors
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