Estoques e mecanismos de estabilização do carbono orgânico do solo em agroecossistemas de clima temperado e sub-tropical

• Ano de defesa: 2009
• Autor(a) principal: Nicoloso, Rodrigo da Silveira
• Tipo de documento: Tese
• Tipo de acesso: Acesso aberto
• Idioma: por
• Instituição de defesa: Universidade Federal de Santa Maria; BR; Engenharia Agrícola; UFSM; Programa de Pós-Graduação em Engenharia Agrícola
• Palavras-chave em Português: Seqüestro de carbono; Agregados; Carbono orgânico particulado; Carbon sequestration; Aggregates; Particulate organic carbon; CNPQ::CIENCIAS AGRARIAS::ENGENHARIA AGRICOLA
• Link de acesso: http://repositorio.ufsm.br/handle/1/3574

Soil carbon (C) sequestration in agriculture soil is a low cost option to mitigate global climatic change. No-till (NT) associated with good husbandry practices could compensate up to 15% of the anthropogenic CO2 emissions by storing the C from atmosphere as soil organic carbon (SOC). To be fully accepted as a mitigation alternative, research must be conducted to improve the accuracy of soil C sequestration estimates on field experiments as well as those made by mathematical models at regional and local scales. Complementarily, is necessary to improve the knowledge about the SOC stabilization mechanisms, delimiting the real soil´s capacity into accumulate C, quantifying how much of the stored C could be re-emitted to the atmosphere by changes in soil management. The present work is divided in four chapters with the objective to answer these questions. The first chapter has the objective to discuss the importance of sampling depth (0-0.30, 0-0.60, and 0-0.90 m) and the definition of a reliable and adequate baseline for the calculation of the C sequestration rates. Two long-term field experiments from a temperate (Mollisol) and a sub-tropical (Oxisol) climate soil were selected for this research. The experiments tested soil tillage systems (conventional tillage (CT) and NT) (Mollisol and Oxisol) and sources and rates of nitrogen amendment on corn in the Mollisol (control without N, 168 kg N ha-1 as ammonium sulfate, and 168 kg N ha-1 as organic fertilizer) and different crop rotation systems in the Oxisol (R0:soybean-wheat, R1:soybean-wheat-soybean-oat, and R2:soybean-oat-soybean-oat+vetch-corn-radish-wheat). The increase of sampling depth provided limited contribution to the estimates of C sequestration rates due to the increase of the error on SOC stocks estimates at deeper soil depths. To improve the C sequestration rate estimates, SOC temporal dynamic analysis should be preferred rather than the comparison of the SOC stocks of paired plots at a unique time point. The second chapter had the objective to apply simple mathematical equations to describe the SOC dynamics and improve the estimates of C sequestration rates and also to understand the role of the macroaggregate formation on SOC accumulation and saturation. The use of linear and kinetic (exponential growth) equation was adequate to describe the SOC dynamics increasing the accuracy of the C sequestration rate estimates by reducing errors promoted by soil spatial variability. The SOC accumulation was a function of the amount of C input to the soil and the macroaggregate formation to protect SOC. The SOC saturation process occurred from the smaller to the larger aggregate size fraction, limiting the capacity of a given superficial soil layer to accumulate SOC. However, the SOC saturation at superficial soil layers did not indicate the end of C sequestration in the soil, since the SOC accumulation occurred at sub-superficial soil layers. In the third chapter, the mathematical approach to determine changes on SOC stocks and the SOC saturation-induced limitation for C sequestration were applied to improve the accuracy of the Hénin e Dupuís (1945) one- 8 compartmental mathematical model into predict future soil C sequestration rates. The long-term field experiment from the Mollisol was selected for this research because of the better data availability (sampling years) and also by the presence of two treatments under CT and NT with SOC saturated soil layers. The mathematical adjustment (by linear equations) of the SOC dynamic coefficients improved the adjustment of the model‟s predictions. The SOC saturation-induced restriction for SOC accumulation on the mathematical model avoided the overestimation of the soil‟s potential for C sequestration. The predictions of the mathematical models indicate that the Mollisol‟s superficial layer (0-0.05 m) under NT could maintain significant C sequestration rates for up to 50 years as a function of the amount of C input to the soil. For the fourth chapter, a detailed study of the SOC pools in water-stable aggregate size fractions by granulometric and densimetric fractionation was carried out. The objective was to identify the pools where SOC accumulation was occurring and what SOC stabilization mechanisms were present. This will provide estimates of the NT potential to promote long-term C sequestration. SOC accumulation occurred preferentially in the more stable and recalcitrant SOC fractions (Mollisol and Oxisol) or in microaggregate and macroaggregate physically protected fractions (Mollisol). In the Oxisol, the SOC enrichment occurred mostly in the mineral associated-SOC fractions extra-microaggregates occluded within meso- and macroaggregates, while in the Mollisol, the SOC accumulation occurred in both intra- and extra-microaggregate mineral associated-SOC fractions. More than 78 and 92% of the C sequestration verified in the Mollisol and Oxisol, respectively, were considered as long-term by occurring in stable SOC fractions.