INFLUENCE OF ORGANIC MATTER ON MEAN SIZE OF CLAY MINERALS IN BASALT SOILS IN SOUTHERN BRAZIL

被引:12
作者
Hanke, Daniel [1 ]
Melo, Vander de Freitas [2 ]
Dieckow, Jeferson [2 ]
Dick, Deborah Pinheiro [3 ]
Bognola, Itamar Antonio [4 ]
机构
[1] Univ Fed Parana, Dept Solos & Engn Agr, Programa Posgrad Ciencia Solo, BR-80060000 Curitiba, Parana, Brazil
[2] Univ Fed Parana, Dept Solos & Engn Agr, BR-80060000 Curitiba, Parana, Brazil
[3] Univ Fed Rio Grande do Sul, Inst Quim, Porto Alegre, RS, Brazil
[4] Empresa Brasileira Pesquisa Agr, Embrapa Florestas, Colombo, Parana, Brazil
来源
REVISTA BRASILEIRA DE CIENCIA DO SOLO | 2015年 / 39卷 / 06期
关键词
dissolution; reduction; complexation; carboxyl; crystal; IRON-OXIDES; GOETHITE; CARBON; DISSOLUTION; KAOLINITE; GIBBSITE;
D O I
10.1590/01000683rbcs20140655
中图分类号
S15 [土壤学];
学科分类号
0903 ; 090301 ;
摘要
The interaction of organic compounds with clay minerals can change the size of crystals. However, in soils this effect is still unclear because of limitations in separation of pure mineral phases for conducting dissolution experiments. In this study, the relationship between soil organic matter (SOM) and mean crystallite size (MCS) of clay minerals from surface and subsurface horizons of soils from a toposequence in Southern Brazil was evaluated. Soil C and N contents were determined and the nature of the SOM functional groups were evaluated by FTIR spectroscopy. The MCS of minerals was assessed by X ray diffraction performed on Fe-oxide free samples and on Fe-concentrated samples. The C and N content and the relative intensities of the FTIR spectra were considered as predictor variables, and the MCS of hematite, goethite, kaolinite, and gibbsite as predicated variables. The C and N content and carboxylic and C-O-alkyl groups showed significant effects on the variation of MCS. The crystallite dimension of the Fe-oxides and kaolinite was inversely affected by these SOM properties. In contrast, the MCS of gibbsite was not affected by the SOM properties. The SOM influence on the MCS of Fe-oxides was attributed to surface complexation reactions and to surface redox reactions that promote a continuous dissolution-precipitation process.
引用
收藏
页码:1611 / 1622
页数:12
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