Use este identificador para citar ou linkar para este item: https://repositorio.inpa.gov.br/handle/1/18729
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dc.contributor.authorLiang, Biqing-
dc.contributor.authorLehmann, Johannes-
dc.contributor.authorSolomon, D.-
dc.contributor.authorKinyangi, James M.-
dc.contributor.authorGrossman, Julie M.-
dc.contributor.authorO'Neill, Brendan E.-
dc.contributor.authorSkjemstad, Jan O.-
dc.contributor.authorThies, Janice E.-
dc.contributor.authorLuizão, Flávio Jesus-
dc.contributor.authorPetersen, James B.-
dc.contributor.authorNeves, Eduardo Goés-
dc.date.accessioned2020-06-15T22:02:46Z-
dc.date.available2020-06-15T22:02:46Z-
dc.date.issued2006-
dc.identifier.urihttps://repositorio.inpa.gov.br/handle/1/18729-
dc.description.abstractBlack Carbon (BC) may significantly affect nutrient retention and play a key role in a wide range of biogeochemical processes in soils, especially for nutrient cycling. Anthrosols from the Brazilian Amazon (ages between 600 and 8700 yr BP) with high contents of biomass-derived BC had greater potential cation exchange capacity (CEC measured at pH 7) per unit organic C than adjacent soils with low BC contents. Synchrotron-based near edge X-ray absorption fine structure (NEXAFS) spectroscopy coupled with scanning transmission X-ray microscopy (STXM) techniques explained the source of the higher surface charge of BC compared with non-BC by mapping cross-sectional areas of BC particles with diameters of 10 to 50 μm for C forms. The largest cross-sectional areas consisted of highly aromatic or only slightly oxidized organic C most likely originating from the BC itself with a characteristic peak at 286.1 eV, which could not be found in humic substance extracts, bacteria or fungi. Oxidation significantly increased from the core of BC particles to their surfaces as shown by the ratio of carboxyl-C/aromatic-C. Spotted and non-continuous distribution patterns of highly oxidized C functional groups with distinctly different chemical signatures on BC particle surfaces (peak shift at 286.1 eV to a higher energy of 286.7 eV) indicated that non-BC may be adsorbed on the surfaces of BC particles creating highly oxidized surface. As a consequence of both oxidation of the BC particles themselves and adsorption of organic matter to BC surfaces, the charge density (potential CEC per unit surface area) was greater in BC-rich Anthrosols than adjacent soils. Additionally, a high specific surface area was attributable to the presence of BC, which may contribute to the high CEC found in soils that are rich in BC. © Soil Science Society of America.en
dc.language.isoenpt_BR
dc.relation.ispartofVolume 70, Número 5, Pags. 1719-1730pt_BR
dc.rightsRestrito*
dc.subjectCarbonen
dc.subjectIon Exchangeen
dc.subjectMicroscopic Examinationen
dc.subjectPh Effectsen
dc.subjectPositive Ionsen
dc.subjectSpectroscopic Analysisen
dc.subjectBiogeochemical Processesen
dc.subjectBlack Carbonen
dc.subjectCation Exchange Capacity (cec)en
dc.subjectScanning Transmission X-ray Microscopy (stxm)en
dc.subjectSoil Surveysen
dc.subjectCarbonen
dc.subjectIon Exchangeen
dc.subjectMicroscopic Examinationen
dc.subjectPh Effectsen
dc.subjectPositive Ionsen
dc.subjectSoil Surveysen
dc.subjectSpectroscopic Analysisen
dc.subjectBiogeochemistryen
dc.subjectBlack Carbonen
dc.subjectIon Exchangeen
dc.subjectOrganic Carbonen
dc.subjectOxidationen
dc.subjectSoil Nutrienten
dc.subjectSoil Organic Matteren
dc.subjectAmazon Riveren
dc.subjectSouth Americaen
dc.subjectBacteria (microorganisms)en
dc.subjectFungien
dc.titleBlack carbon increases cation exchange capacity in soilsen
dc.typeArtigopt_BR
dc.identifier.doi10.2136/sssaj2005.0383-
dc.publisher.journalSoil Science Society of America Journalpt_BR
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