Effects of fire on soil organic matter in northern Amazonian forest fragments / Efeitos do fogo sobre a matéria orgânica do solo em fragmentos de floresta no norte da Amazônia

Forest fires incorporate pyrogenic organic matter into the soil, affecting the characteristics of soil organic matter (SOM) due to its high aromaticity, increasing its renewal time. However, the factors that control the concentration of pyrogenic organic matter and its chemical composition and structure are still little known. Forest fragments dispersed in a savanna matrix of the northern Brazilian Amazon are frequently impacted by fires, which can affect the composition of SOM within the fragments. The aim of this study was to analyse the chemical composition of SOM in the border and interior of six forest fragments in the Roraima savanna, in the northern Brazilian Amazon. Soil samples were collected at 10-cm intervals up to 1 m in depth at the border and in the interior of each fragment. Soil organic material concentration was determined with 10% HF solution and its elemental composition, thermogravimetric index, and 13C CPMAS NMR spectroscopic analysis were determined. There was no significant difference in the aromaticity index between border and interior. The concentration of alkyl C structures between border (22 to 25%) and interior (19 to 29%) indicated the occurrence of medium-intensity fires in the study area. The thermogravimetric analysis showed no significant difference in the thermal stability of SOM between border and interior. Our results showed no pronounced difference in SOM quality up to 1 m depth between the border and the interior of the evaluated forest fragments, indicating that this compartment is stable throughout the fragments.(AU)

Incêndios florestais incorporam matéria orgânica pirogênica ao solo, afetando as características da matéria orgânica do solo (MOS), devido a sua alta aromaticidade. Porém, os fatores que controlam a composição química e a estrutura da matéria orgânica pirogência ainda são pouco conhecidos. Fragmentos florestais dispersos em uma matriz de savana na Amazônia setentrional brasileira são freqüentemente impactados por incêndios, que podem afetar a composição da MOS nos fragmentos. O objetivo deste estudo foi analisar a composição química da MOS na borda e no interior de seis fragmentos florestais situados na savana de Roraima, norte da Amazônia brasileira. Amostras de solo foram coletadas em intervalos de 10 cm até 1 m de profundidade na borda e no interior de cada fragmento. A concentração da MOS foi determinada com solução de HF a 10% e sua composição elementar, índice termogravimétrico e análise espectroscópica de 13C CPMAS RMN foram determinados. Não houve diferença significativa no índice de aromaticidade entre borda e interior. A concentração de estruturas alquil C entre a borda (22 a 25%) e o interior (19 a 29%) indicou a ocorrência de incêndios de média intensidade na área de estudo. A análise termogravimétrica não mostrou diferença significativa na estabilidade térmica da matéria orgânica do solo entre a borda e o interior. Nossos resultados não mostraram diferença pronunciada na qualidade da MOS até 1 m de profundidade entre a borda e o interior dos fragmentos florestais avaliados, indicando que este compartimento é estável ao longo dos fragmentos.(AU)

Atrazine degradation patterns: the role of straw cover and herbicide application history

In Brazil, atrazine (ATZ) is widely applied to maize (Zea mays L.) fields for weed control. The presence of ATZ and its metabolites in soil and water matrices has become a matter of some concern for governmental authorities as well as for society at large. This study evaluated the patterns of ATZ degradation (mineralization, extractable and non-extractable ATZ residues, and metabolite formation) in a Brazilian Typic Paleudult. Soil samples from a cultivated area under a no-tillage system with a history of ATZ application were incubated with 14C-ATZ in both the presence and absence of straw cover on the soil surface, and the evolved 14CO2 was determined by liquid scintillation. Samples from an area with native vegetation, adjacent to the cultivated area, were also incubated as a control. A higher mineralization of ATZ was observed in the cultivated soil (> 85 %) in comparison with the native soil (10 %) after 85 days of incubation. In addition to the higher mineralization and hydroxyatrazine (HA) formation, a rapid decrease in the water-extractable residues was observed in the cultivated soil. When the cultivated soil was covered with straw, mineralization was reduced by up to 30 % although a small amount of remobilization to the soil occurred within the 85 days. Straw cover hindered the degradation of ATZ in cultivated soils; whereas an accelerated biodegradation was due to repeated applications of ATZ, which may have selected microbiota more skilled at biodegrading the herbicide.

Atrazine degradation patterns: the role of straw cover and herbicide application history

In Brazil, atrazine (ATZ) is widely applied to maize (Zea mays L.) fields for weed control. The presence of ATZ and its metabolites in soil and water matrices has become a matter of some concern for governmental authorities as well as for society at large. This study evaluated the patterns of ATZ degradation (mineralization, extractable and non-extractable ATZ residues, and metabolite formation) in a Brazilian Typic Paleudult. Soil samples from a cultivated area under a no-tillage system with a history of ATZ application were incubated with 14C-ATZ in both the presence and absence of straw cover on the soil surface, and the evolved 14CO2 was determined by liquid scintillation. Samples from an area with native vegetation, adjacent to the cultivated area, were also incubated as a control. A higher mineralization of ATZ was observed in the cultivated soil (> 85 %) in comparison with the native soil (10 %) after 85 days of incubation. In addition to the higher mineralization and hydroxyatrazine (HA) formation, a rapid decrease in the water-extractable residues was observed in the cultivated soil. When the cultivated soil was covered with straw, mineralization was reduced by up to 30 % although a small amount of remobilization to the soil occurred within the 85 days. Straw cover hindered the degradation of ATZ in cultivated soils; whereas an accelerated biodegradation was due to repeated applications of ATZ, which may have selected microbiota more skilled at biodegrading the herbicide.(AU)

Carbon sequestration in clay and silt fractions of Brazilian soils under conventional and no-tillage systems

The capacity of soils to sequestrate carbon (C) is mainly related to the formation of organo-mineral complexes. In this study, we investigated the influence of soil management systems on the C retention capacity of soil with an emphasis on the silt and clay fractions of two subtropical soils with different mineralogy and climate. Samples from a Humic Hapludox and a Rhodic Hapludox, clayey soils cultivated for approximately 30 years under no-tillage (NT) and conventional tillage (CT) were collected from six layers distributed within 100-cm soil depth from each site and from an adjacent native forest. After the removal of particulate organic matter (POM), the suspension ( 53 µm) was sonicated, the silt and clay fractions were separated in accordance with Stokes' law and the carbon content of whole soil and physical fractions was determined. In the Humic Hapludox, the clay and silt fractions under NT showed a higher maximum C retention (72 and 52 g kg-1, respectively) in comparison to those under CT (54 and 38 g kg-1, respectively). Moreover, the C concentration increase in both fractions under NT occurred mainly in the topsoil (up to 5 cm). The C retention in physical fractions of Rhodic Hapludox varied from 25 to 32 g kg-1, and no difference was observed whether under an NT or a CT management system. The predominance of goethite and gibbsite in the Humic Hapludox, as well as its exposure to a colder climate, may have contributed to its greater C retention capacity. In addition to the organo-mineral interaction, a mechanism of organic matter self-assemblage, enhanced by longer periods of soil non-disturbance, seems to have contributed to the carbon stabilization in both soils.

Carbon sequestration in clay and silt fractions of Brazilian soils under conventional and no-tillage systems

The capacity of soils to sequestrate carbon (C) is mainly related to the formation of organo-mineral complexes. In this study, we investigated the influence of soil management systems on the C retention capacity of soil with an emphasis on the silt and clay fractions of two subtropical soils with different mineralogy and climate. Samples from a Humic Hapludox and a Rhodic Hapludox, clayey soils cultivated for approximately 30 years under no-tillage (NT) and conventional tillage (CT) were collected from six layers distributed within 100-cm soil depth from each site and from an adjacent native forest. After the removal of particulate organic matter (POM), the suspension ( 53 µm) was sonicated, the silt and clay fractions were separated in accordance with Stokes' law and the carbon content of whole soil and physical fractions was determined. In the Humic Hapludox, the clay and silt fractions under NT showed a higher maximum C retention (72 and 52 g kg-1, respectively) in comparison to those under CT (54 and 38 g kg-1, respectively). Moreover, the C concentration increase in both fractions under NT occurred mainly in the topsoil (up to 5 cm). The C retention in physical fractions of Rhodic Hapludox varied from 25 to 32 g kg-1, and no difference was observed whether under an NT or a CT management system. The predominance of goethite and gibbsite in the Humic Hapludox, as well as its exposure to a colder climate, may have contributed to its greater C retention capacity. In addition to the organo-mineral interaction, a mechanism of organic matter self-assemblage, enhanced by longer periods of soil non-disturbance, seems to have contributed to the carbon stabilization in both soils.(AU)

Solos subtropicais de altitude: atributos químicos, teor de matéria orgânica e resistência à oxidação química / Highland subtropical soils: chemical attributes, content of organic matter and its resistance to chemical oxidation

Neste trabalho foram estudadas amostras de horizontes A de oito solos representativos da região Campos de Cima da Serra, Rio Grande do Sul, sendo determinados: textura, pH em água, CTC a pH 7, teores de Al trocável e de óxidos de Fe (Fed e Feo). As amostras foram tratadas com peróxido de hidrogênio e, antes e após tratamento, foram determinados teores de C e de N e realizada análise por espectroscopia de infra-vermelho com transformada de Fourier (FTIR). O teor de C foi alto (4 a 23 por cento) e sua variação correlacionou-se com a altitude e com o teor de Al trocável, sugerindo que a menor temperatura e a complexação com Al iônico contribuem para a estabilização da matéria orgânica do solo (MOS). A proporção de carbono do solo resistente à oxidação variou de 1 a 16 por cento e correlacionou-se com a razão Feo/Fed. A estabilização desta fração da MOS foi atribuída à interação de grupos carboxílicos ligados a estruturas alifáticas e aromáticas com óxidos de Fe de baixa cristalinidade.(AU)

In this research, texture, soil pH, CEC at pH 7, exchangeable Al, and content of Fe-oxides (Fed and Feo) were determined in A horizons samples of eight representative soils under native pasture from Campos de Cima da Serra, Rio Grande do Sul State, Brazil. The samples were treated with hydrogen peroxide and, before and after the treatment, C and N contents were determined and Fourier Transformed Infra-red (FTIR) spectroscopy was performed. The content of soil C was high (4 to 23 percent) and its variation correlated with the altitude and exchangeable Al indicating that lower temperatures and complexation with ionic Al contribute to soil organic matter (SOM) stabilization. The proportion of oxidation-resistant carbon varied between 1 and 16 percent and correlated with the ratio Feo/Fed. The stabilization of this SOM fraction was assigned to the interaction of carboxylic groups bound to aromatic and aliphatic structures with Fe-oxides of low crystallinity degree.(AU)