RESUMO 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.

ABSTRACT 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.

ABSTRACT Bases are chemical species that donate electrons, accept protons, or release hydroxyls (OH–) in aqueous solution. In Soil Science, “base saturation”, “exchangeable bases” or “basic cations” has been widely used to distinguish Ca2+, Mg2+, Na+, and K+ from H+ and Al3+ cations. This terminology is confusing since none of these cations are truly a base in chemistry sense. However, in the absence of the proposition of a correct term, the term “base saturation” remains in use nowadays, causing confusion among students, professionals, and even among professors and researchers in Soil Science, as it leads to the erroneous interpretation that the soil acidity can be corrected by adding these cations to the soil. Here, we present the historical background of this nomenclature and a theoretical foundation that justifies the abolition of the use of these terms in Soil Science. We consider that the most correct is to call it “Ca-Mg-K-Na saturation”, which, despite being long, would refer directly and without any misinterpretation of the terminology. In Soil Fertility, the “base saturation” is often calculated only as a function of the sum of Ca, Mg, and K, since the Na content is negligible in most tropical and subtropical soils. Thus, one could use the term “Ca-Mg-K saturation”. Likewise, it is also suggested to abolish the use of the term “sum of bases” and use the term “sum of Ca-Mg-K” or “sum of Ca-Mg-K-Na” instead when necessary.

ABSTRACT: 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.

ABSTRACT Aggregate stability is one of the most important factors in soil conservation and maintenance of soil environmental functions. The objective of this study was to investigate the aggregate stability mechanisms related to chemical composition of organic matter in soil profiles with humic and histic horizons in a toposequence under Araucaria moist forest in southern Brazil. The soils sampled were classified as Humic Hapludox (highest position), Fluvaquentic Humaquepts (lowest slope position), and Typic Haplosaprists (floodplain). The C and N contents were determined in bulk soil samples. The chemical composition of soil organic matter was evaluated by infrared spectroscopy. Aggregate stability was determined by applying increasing levels of ultrasound energy. Carbon content increased from the top of the slope to the alluvial plain. Higher ultrasonic energy values for clay dispersion were observed in the C-rich soils in the lower landscape positions, indicating that organic compounds play an important role in the structural stabilization of these profiles. Both aliphatic and carbohydrate-like structures were pertinent to aggregate stability. In the Oxisol, organo-mineral interaction between carbohydrates and the clay mineral surface was the most important mechanism affecting aggregation. In soils with a higher C content (Humaquepts and Haplosaprists), stabilization is predominantly conferred by the aliphatic groups, which is probably due to the structural protection offered by these hydrophobic organic groups.

ABSTRACT Soils with humic and histic horizons in tropical and subtropical ecosystems play an important role in determining the atmospheric C stock and its stabilization, climate regulation, water holding capacity, and environmental filtering, due to the different functions of soil organic matter (SOM). However, the processes and mechanisms that regulate SOM dynamics in these soils are not clear. The objectives of this study were: i) determine the C and N stocks and ii) investigate the SOM chemical fractions and their interactions with Fe and Al ions in soils with humic and histic horizons of a toposequence under Araucaria moist forest in southern Brazil. The soils sampled were classified as Humic Hapludox (top - not hydromorphic), Fluvaquentic Humaquepts (lower third - hydromorphic), and Typic Haplosaprists (floodplain - hydromorphic). The C and N contents were determined in bulk soil samples and SOM chemical fractions; in these fractions, Fe and Al co-extracted contents were also determined. The chemical composition of humin and humic acid fractions was investigated by FTIR spectroscopy. The C content in the toposequence increased from the top to the lowest position. The differences observed in SOM content and SOM chemical composition were defined by the differences in soil water regime. The amount of C stored in the subsurface horizons is about 70 % of total organic C. The carbohydrate-like structures in the humin fraction were protected from solubilization through interaction with iron oxides, which may represent an important mechanism for labile organic compound preservation in these soils. The soluble humic substances showed the highest Fe and Al contents, and their compartments have different affinities for Fe and Al.

The goal of this study was to investigate the effect of composted pig slurry (PS) on the organic matter concentration and distribution of humic acid (HA), fulvic acid (FA) and humin (HU) fractions. The fractions were quantified following the addition of composted PS to the soil, which was produced with no acidification (T2) or with acidification with H3PO4 (T3); and in soil without compost addition (T1). The HA chemical composition was analyzed by FTIR spectroscopy. The addition of the two composts did not change the soil carbon concentration but affected the distribution of the humic fractions. For the three treatments, the carbon concentration of humic substances increased until 52 days following compost addition, with more pronounced increases with the addition of non-acidified PS compost (14.5 g kg-1) and acidified PS compost (15.1 g kg-1). This increase was reflected in both the FA and HA concentrations. The addition of compost with PS acidification resulted in the formation of larger humic micelles (HA) with higher aromatic content and fewer functional groups than the non-acidified PS compost. These findings, together with a lower proportion of carbohydrate-type structures, indicated the presence of more stable humic micelles in the soil treated with acidified PS compost.

RESUMO A produção de resíduos orgânicos durante os processos agroindustriais é um problema tanto ambiental quanto econômico devido às características químicas desses resíduos. Geralmente, resíduos orgânicos estabilizados servem como condicionadores de solos. Esses resíduos podem afetar tanto na composição química quanto nas características das cargas trocáveis dos solos. O objetivo deste trabalho foi avaliar a formação de substâncias húmicas (SH) durante a vermicompostagem em diferentes resíduos agroindustriais, bem como caracterizar a composição química e molecular. Assim, diferentes resíduos - esterco bovino (EB), esterco ovino (EO), restos de alimentos de restaurantes (RA), lodo de arroz parboilizado (LP), restos de frutas e vegetais (RF) - foram submetidos à vermicompostagem. Amostras desses materiais foram secas, trituradas e caracterizadas quimicamente quanto a pH, carbono (C) orgânico, N total, Ca, Mg, K, P, relação C/N, e condutividade elétrica (CE) antes, durante e depois do processo de vermicompostagem. Além disso, foi analisado o fracionamento da matéria orgânica como as SH, análise elementar e espectroscopia de infravermelho. De acordo com o processo de vermicompostagem dos resíduos agroindustriais, o carbono orgânico total (COT) e os ácidos fúlvicos (AF) foram reduzidos; contudo, os ácidos húmicos (AH) aumentaram proporcionalmente. Dentre os vermicompostos estudados diferiram quanto à proporção final de SH formadas decrescendo na sequência: EB>RF>EO>RA>LP. Isso demonstra uma estabilização dos compostos orgânicos por meio da vermicompostagem, podendo, consequentemente, ser utilizados com uma maior segurança na agricultura.

ABSTRACT The production of organic waste during the agro-industrial processes is a problem for both environmental and economical issues due to the chemical characteristics of these wastes. Generally, stabilized organic residues are used as soil conditioners. These residues can affect both the chemical composition and the characteristics of exchangeable charges of the soils. The aim of this study was to evaluate the formation of humic substances during the vermicomposting of different agro-industrial solid residues, as well as characterize the chemical and molecular composition. So, different residues (bovine manure (EB), sheep manure (EO); food waste from restaurants (RA); mud of parboiled rice (LP); waste of fruits and vegetables (RF)) were subjected to vermicomposted. Samples of these materials were dried, smashed and chemically characterized as pH, organic carbon, total nitrogen, Ca, Mg, K, P, C/N ratio, and electrical conductivity (EC) before, during and after the vermicomposting process. In addition, it was analyzed the fractionation of organic matter such as humic substances, elemental analysis and infrared spectroscopy. According to the vermicomposting process of agro-industrial wastes, the total organic carbon and fulvic acids were reduced; however, humic acids increased proportionately. Among the studied vermicomposts, they differ in the final ratio of humic substances formed decreasing following: EB>RF>AND>RA>LP. This demonstrates a stabilization of organic compounds through the vermicompost process, and therefore can be used with greater safety in agriculture.

RESUMO A interação de compostos orgânicos com minerais de argila pode alterar o tamanho dos cristais. No entanto, em solos, esse efeito é ainda pouco claro por causa das limitações na separação de fases puras de minerais para realizar experimentos de dissolução. Neste estudo, a relação entre a matéria orgânica do solo (MOS) e diâmetro médio do cristal (DMC) de minerais de argila de horizontes superficiais e subsuperfíciais de solos de uma topossequência no sul do Brasil foi avaliada. Os teores de C e N foram determinados, e a natureza dos grupos funcionais da MOS foi avaliada por espectroscopia de FTIR. O DMC dos minerais foi avaliado por difração de raios X, em umas amostras desferrificadas e outras com óxidos de Fe concentrados. Os teores de C e N e as intensidades relativas dos espectros de FTIR foram considerados como variáveis preditoras; e o DMC de hematita, goethita, caulinita e gibbsita, como variáveis preditas. Os teores de C e N e os grupos carboxílicos e C-O-Alquil evidenciaram efeito significativo sobre a variação do DMC. A dimensão dos cristais de óxidos de Fe e de caulinita foi inversamente correlacionada com esses atributos da MOS. Em contraste, o DMC de gibbsita não foi influenciado pelos atributos dae MOS. A influência da MOS sobre o DMC dos óxidos de Fe foi atribuída às reações de complexação de superfície e de redox, que promovem um processo contínuo de dissolução-precipitação.

ABSTRACT 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.

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.

A utilização de herbicidas com formulações com liberação controlada poderá se constituir em uma ferramenta importante para reduzir problemas de lixiviação e garantir a eficácia desses produtos. O objetivo do presente trabalho foi comparar a eficiência de controle de Urochloa plantaginea (UROPL) e o rendimento de grãos de milho entre uma formulação de atrazina comercial (WG) e uma formulação de liberação controlada (xerogel). O delineamento utilizado foi o de blocos ao acaso, em parcelas subdivididas, com quatro repetições, em um esquema (2x7)+1. Nas parcelas principais, foram locadas as formulações de atrazina (WG e xerogel) e, nas subparcelas, as concentrações dos herbicidas (0, 2400, 3200, 3600, 4200, 5400 e 8000g de atrazina ha-1). Foram determinados os níveis de controle e densidade de plantas de UROPL e o rendimento de grãos da cultura do milho. A elevação das doses de atrazina resultou em aumento dos níveis de controle de UROPL. Em avaliações realizadas aos 28 e 35 dias após a aplicação, a atrazina xerogel demonstrou eficiência agronômica superior à formulação WG. Não ocorreram diferenças de rendimento de grãos de milho em parcelas tratadas com diferentes formulações e níveis de atrazina.

The use of herbicides with controlled release formulations may constitute important tool to reduce leaching problems and increase the efficacy of atrazine in soil. The aim of this study was to compare the efficiency of control of Urochloa plantaginea (UROPL) and corn grain yield from a commercial formulation (WG) of atrazine and a controlled-release formulation (xerogel). The design was randomized blocks in split plots with four replications in a scheme (2x7)+1. Factor A consisted of the formulations of atrazine (WG and xerogel), factor B concentrations of herbicide (0, 2400, 3200, 3600, 4200, 5400 and 8000ha atrazine g-1). Variables assessed consisted of control levels, plant density of UROPL and corn grain yield. The increasing levels of atrazine resulted in increased levels of control UROPL. In assessments made at 28 and 35 days after application, atrazine xerogel showed higher agronomic efficiency than the WG formulation. There were no differences in corn grain yield from plots treated with different formulations and atrazine levels.

A avaliação da qualidade do solo depende do uso de indicadores e índices construídos com as propriedades dele. Entretanto, essas propriedades podem variar entre tipos de uso do solo, bem como interferir nas propriedades do solo usadas para construir os índices. Objetivou-se com este estudo determinar a capacidade de propriedades intrínsecas do solo (teor de argila e óxido de ferro) para explicar as propriedades variáveis (soma de bases, acidez potencial, carbono orgânico, porosidade e densidade) em diferentes usos do solo (floresta nativa, plantio direto e agricultura convencional) em pequenas propriedades familiares no sul do Brasil. Os resultados evidenciaram que as cinco propriedades do solo estudadas podem ser incluídas em avaliações de qualidade e não são influenciadas pelo teor de argila e óxido de ferro. Sugeriu-se que, para solos pouco intemperizados, ricos em filossilicatos do tipo 1:1 e 2:1, se o teor de argila estiver em um intervalo de aproximadamente 200 g kg-1 e o de óxido de ferro for menor que aproximadamente 15 g kg-1, o uso do solo é o maior fator para controlar as propriedades físico-químicas da camada superficial do solo.

The assessment of soil quality is based on indicators and indices derived from soil properties. However, intrinsic soil properties may interfere with other soil properties that vary under different land uses and are used to calculate the indices. The aim of this study was to assess the extent to which intrinsic soil properties (clay and iron oxide contents) explain variable soil properties (sum of bases, potential acidity, organic carbon, total porosity, and bulk density) under different land uses (native forest, no-tillage and conventional agriculture) on small family farms in Southern Brazil. The results showed that the five properties evaluated can be included in soil quality assessments and are not influenced by the clay and iron oxide contents. It was concluded that for little weathered 1:1 and 2:1 phyllosilicate rich-soils, if the difference between the maximum and the minimum clay content under the different land uses is less than about 200 g kg-1 and the iron oxide content less than about 15 g kg-1, the physico-chemical soil properties in the surface layer are determined mostly by the land use.

A interferência antrópica no solo tem modificado a formação original nos Campos de Cima da Serra. O estudo objetivou avaliar a distribuição das substâncias húmicas em um Latossolo sob campo nativo (CN), campo nativo queimado (CNq), mata nativa (MN), florestamento de pinus (FP) e lavoura (LA). Os teores de C orgânico total (COT) e de C em compartimentos químicos da matéria orgânica do solo (MOS) foram determinados. Os usos e manejos adotados no solo afetaram os teores de COT e do C nos compartimentos da MOS. Com relação ao ambiente CN, a MN aumentou o teor de COT, o qual se manteve equivalente no manejo com queima e foi reduzido pelos usos do solo com LA e FP. As alterações de uso e manejo do solo tenderam a reduzir o C nas frações húmicas e modificaram a distribuição das frações ácidos húmicos e fúlvicos.

The anthropic interference have changed the original soil condition in Campos de Cima da Serra region, Brazil. This study aimed to evaluate the distribution of humic substances in an Oxisol under native pasture (CN), native burned pasture (CNq), native forest (MN), pine afforestation (FP) and annual crops (LA). The levels of total organic carbon (TOC) and C compartments of chemical soil organic matter (SOM) were determined. The use and management adopted affected the levels of TOC and C in the chemical compartments of the SOM. In comparison to CN, the MN increased the amounts of TOC, which remained unchanged in the CNq and was reduced by land uses with LA and FP. Changes in land use and management tended to reduce the C in humic fractions and modified the humic and fulvic acids distribution.

A interferência antrópica tem modificado a condição original do solo nos Campos de Cima da Serra. O estudo avaliou atributos químicos e físicos de um Latossolo sob campo nativo (CN), campo nativo manejado com queima (CNq), mata nativa (MN), florestamento de pinus (FP) e lavoura em sistema plantio convencional (LA), nas camadas de 0,00-0,025, 0,025-0,05, 0,05-0,10, 0,10-0,20, 0,20-0,30m. A mineralogia foi avaliada por difratometria de raios X. Foram avaliados o C orgânico total (COT), pH (H2O); Ca, Mg, K, Na e Al trocáveis; H+Al e P; e calculou-se a soma de bases, a capacidade de troca de cátions, a saturação por bases e por Al. Estimou-se a área superficial específica (ASE) e a capacidade máxima de adsorção de fósforo (CMAP). O solo apresentou mineralogia caulinítica e oxídica. No CN, o COT variou entre 15,3 e 56,4g kg-1, o pH foi ≤4,8, a CTC foi alta (18<CTCpH7<22cmol c dm-3), com baixa saturação por bases (3<V<34%) e alta saturação por Al (23<m<88%). Em comparação ao CN, o COT aumentou em superfície na MN, foi equivalente no CNq e diminuiu sob FP e LA. A fertilidade do solo aumentou sob MN e CNq, e foi reduzida sob FP, tendo sido condicionada pelo teor de COT. O COT mostrou relação positiva com a ASE e negativa com a CMAP do solo.

The original landscape of Campos de Cima da Serra region has changed by anthropogenic interference. The study aimed to evaluate soil chemical and physical attributes of an Oxisol under natural grassland (CN), burned natural grassland (CNq), natural forest (MN), pine afforestation (PF) and annual crops in conventional tillage system (LA), in the 0.00-0.025, 0.025-0.05, 0.05-0.10, 0.10-0.20, 0.20-0.30m layers. The mineralogy was evaluated by X-ray diffraction. It was evaluated the total organic carbon (TOC); pH (H2O); exchangeable Ca, Mg, K, Na and Al; H+Al and P contents; and calculated bases sum (S), cation exchange capacity (CEC) and bases and Al saturation on CEC. It was estimated soil specific surface area (SSA) and maximum phosphorus adsorption capacity (MPAC). The soil showed kaolinitic and oxidic mineralogy. In the CN soil TOC content ranged between 15.3 and 56.4g kg-1, pH values ≤4.8; CEC was high (18<CECpH7<22 cmol c dm-3) with low bases saturation (3<V<34%) and high Al saturation (23<m<88%). Related to CN soil, TOC contents increased in the MN surface was similar for the CNq and decreased for the FP and LA areas. Soil fertility was positively modified in MN and CNQ areas, and reduced under FP, and was conditioned by TOC. The TOC content was positively related to soil ASE and negatively with soil MPAC.

O objetivo deste trabalho foi avaliar o padrão de distribuição e a composição da matéria orgânica do solo (MOS) e de seus compartimentos físicos em um Neossolo periodicamente afetado pelo fogo nos últimos 100 anos, no Sul do Brasil. Amostras de solo foram coletadas nas profundidades de 0-5, 5-10 e 10-15 cm, nos seguintes ambientes: pastagem nativa sem queima há um ano e com lotação de 0,5 animal por hectare por ano (1NB); pastagem nativa sem queima há 23 anos e com lotação de 2,0 animais por hectare por ano (23NB); e mata de Araucária (AF). Fracionamento físico foi realizado com amostras das camadas de 0-5 e 5-10 cm. Os estoques de C e N do solo foram determinados nas três profundidades e nas frações físicas, e a matéria orgânica foi caracterizada por espectroscopia de infravermelho e termogravimetria. O maior estoque de C em todas as profundidades e as frações físicas foi verificado na AF. O ambiente 23NB apresentou o menor estoque de C e N do solo na profundidade de 5-15 cm, associado ao cessar fogo e à maior densidade de pastejo. A MOS da fração leve oclusa apresentou maior recalcitrância química em 1NB do que em 23NB. A queima anual da pastagem não afeta o estoque de C até 15 cm de profundidade.

The objective of this work was to evaluate the distribution pattern and composition of soil organic matter (SOM) and its physical pools of Leptosols periodically affected by fire over the last 100 years in South Brazil. Soil samples at 0-5, 5-10, and 10-15 cm depths were collected from the following environments: native pasture without burning in the last year and grazed with 0.5 livestock per hectare per year (1NB); native pasture without burning in the last 23 years and grazed with 2.0 livestock per hectare per year (23NB); and an Araucaria forest (AF). Physical fractionation was performed with the 0-5 and 5-10 cm soil layers. Soil C and N stocks were determined in the three depths and in the physical pools, and organic matter was characterized by infrared spectroscopy and thermogravimetry. The largest C stocks in all depths and physical pools were found under the AF. The 23NB environment showed the lowest soil C and N stocks at the 5-15 cm depth, which was related to the end of burning and to the higher grazing intensity. The SOM of the occluded light fraction showed a greater chemical recalcitrance in 1NB than in 23NB. Annual pasture burning does not affect soil C stocks up to 15 cm of depth.

Distribution and stocks of soil organic matter (SOM) compartments after Pinus monoculture introduction in a native pasture area of a Cambisol, Santa Catarina, Brazil, were investigated. Pinus introduction increased soil acidity, content of exchangeable Al+3 and diminished soil nutrients. Nevertheless, soil C stock increased in all humic fractions of the 0-5 cm layer after Pinus afforestation. In the subsurface, the vegetation change only promoted SOM redistribution from the NaOH-extractable humic substances to a less hydrophobic humin fraction. Under Pinus, soil organo-mineral interactions were relevant up to a 15 cm depth, while in pasture environment, this mechanism occurred mainly in the surface layer.