Al-/Fe-(hydr)oxides–organic carbon associations in Oxisols — From ecosystems to submicron scales

Detalhes bibliográficos
Autor(a) principal: Souza, Ivan F.
Data de Publicação: 2017
Outros Autores: Archanjo, Bráulio S., Hurtarte, Luis C.C., Oliveros, Martin E., Gouvea, Cristol P., Lidizio, Leandro R., Achete, Carlos A., Schaefer, Carlos E.R., Silva, Ivo R.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: LOCUS Repositório Institucional da UFV
Texto Completo: https://doi.org/10.1016/j.catena.2017.02.017
http://www.locus.ufv.br/handle/123456789/21385
Resumo: Al-/Fe(hydr)oxides accumulation upon weathering favors soil organic carbon (SOC) protection into mineral-organic associations (MOAs). Paradoxically, tropical ecosystems on highly weathered soils are characterized by high turnover rates of SOC. Our objective was to propose an explanation for such apparent contradiction by inferring the chemical composition of MOAs in Oxisols. To this end, we compiled a large data set from 43 published articles providing chemical and physical properties of 179 Oxisols/Ferralsols and their SOC content in the A horizon. Thermal analysis (TA) coupled to evolved gas detection (EGD) was used to assess mineral dehydroxylation and SOC oxidation in two soils with contrasting SOC content. Scanning transmission electron microscopy (STEM) was used to probe MOAs within the soil fraction < 53 μm. At large scales, SOC content was strongly correlated to Al extractable by both ammonium oxalate (AO) (r = 0.71) and dithionite-citrate-bicarbonate (DCB) (r = 0.41). Weaker, but significant correlations occurred for SOC against Fe-AO and Fe-DCB (r = 0.38, and r = 014, respectively). At micro-scale, SOC also was found associated to Al-/Fe-(hydr)oxides, as inferred from the STEM imaging. TA-EGD indicated that with increasing SOC content, proportionally more organic matter was oxidized following the dehydroxylation of Al-/Fe-(hydr)oxides at temperatures < 400 °C. Within the first 20 cm of the topsoil of the Oxisols included in our data set, Al-AO explained 62% of the total variation in SOC. However, while SOC content varied from 0.8 up to 145.8 g kg− 1 soil, Al-AO varied between 0.2 and 15.3 g kg− 1 soil. From the perspective of mineral control on SOC retention, reactive species of Al-(hydr)oxides should interact with a disproportionally large amount of organic matter. Because mineral protection is seemingly reduced upon increasing C content in MOAs, SOC in Oxisols may be more vulnerable to environmental changes than currently recognized.
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spelling Souza, Ivan F.Archanjo, Bráulio S.Hurtarte, Luis C.C.Oliveros, Martin E.Gouvea, Cristol P.Lidizio, Leandro R.Achete, Carlos A.Schaefer, Carlos E.R.Silva, Ivo R.2018-08-23T13:45:02Z2018-08-23T13:45:02Z2017-070341-8162https://doi.org/10.1016/j.catena.2017.02.017http://www.locus.ufv.br/handle/123456789/21385Al-/Fe(hydr)oxides accumulation upon weathering favors soil organic carbon (SOC) protection into mineral-organic associations (MOAs). Paradoxically, tropical ecosystems on highly weathered soils are characterized by high turnover rates of SOC. Our objective was to propose an explanation for such apparent contradiction by inferring the chemical composition of MOAs in Oxisols. To this end, we compiled a large data set from 43 published articles providing chemical and physical properties of 179 Oxisols/Ferralsols and their SOC content in the A horizon. Thermal analysis (TA) coupled to evolved gas detection (EGD) was used to assess mineral dehydroxylation and SOC oxidation in two soils with contrasting SOC content. Scanning transmission electron microscopy (STEM) was used to probe MOAs within the soil fraction < 53 μm. At large scales, SOC content was strongly correlated to Al extractable by both ammonium oxalate (AO) (r = 0.71) and dithionite-citrate-bicarbonate (DCB) (r = 0.41). Weaker, but significant correlations occurred for SOC against Fe-AO and Fe-DCB (r = 0.38, and r = 014, respectively). At micro-scale, SOC also was found associated to Al-/Fe-(hydr)oxides, as inferred from the STEM imaging. TA-EGD indicated that with increasing SOC content, proportionally more organic matter was oxidized following the dehydroxylation of Al-/Fe-(hydr)oxides at temperatures < 400 °C. Within the first 20 cm of the topsoil of the Oxisols included in our data set, Al-AO explained 62% of the total variation in SOC. However, while SOC content varied from 0.8 up to 145.8 g kg− 1 soil, Al-AO varied between 0.2 and 15.3 g kg− 1 soil. From the perspective of mineral control on SOC retention, reactive species of Al-(hydr)oxides should interact with a disproportionally large amount of organic matter. Because mineral protection is seemingly reduced upon increasing C content in MOAs, SOC in Oxisols may be more vulnerable to environmental changes than currently recognized.engCATENAvolume 154, páginas 63-72, julho 2017Elsevier B.V.info:eu-repo/semantics/openAccessAl-/Fe-(hydr)oxidesCarbonOxisolsFerralsolsSubtropicsTropicsAl-/Fe-(hydr)oxides–organic carbon associations in Oxisols — From ecosystems to submicron scalesinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfreponame:LOCUS Repositório Institucional da UFVinstname:Universidade Federal de Viçosa (UFV)instacron:UFVORIGINALartigo.pdfartigo.pdftexto completoapplication/pdf1657714https://locus.ufv.br//bitstream/123456789/21385/1/artigo.pdf3348491430b9e41be0f963536c776393MD51LICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://locus.ufv.br//bitstream/123456789/21385/2/license.txt8a4605be74aa9ea9d79846c1fba20a33MD52THUMBNAILartigo.pdf.jpgartigo.pdf.jpgIM Thumbnailimage/jpeg6478https://locus.ufv.br//bitstream/123456789/21385/3/artigo.pdf.jpg52b470b6f0043b0ff31ccb98387d9bd7MD53123456789/213852018-08-23 23:00:46.812oai:locus.ufv.br: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Repositório InstitucionalPUBhttps://www.locus.ufv.br/oai/requestfabiojreis@ufv.bropendoar:21452018-08-24T02:00:46LOCUS Repositório Institucional da UFV - Universidade Federal de Viçosa (UFV)false
dc.title.en.fl_str_mv Al-/Fe-(hydr)oxides–organic carbon associations in Oxisols — From ecosystems to submicron scales
title Al-/Fe-(hydr)oxides–organic carbon associations in Oxisols — From ecosystems to submicron scales
spellingShingle Al-/Fe-(hydr)oxides–organic carbon associations in Oxisols — From ecosystems to submicron scales
Souza, Ivan F.
Al-/Fe-(hydr)oxides
Carbon
Oxisols
Ferralsols
Subtropics
Tropics
title_short Al-/Fe-(hydr)oxides–organic carbon associations in Oxisols — From ecosystems to submicron scales
title_full Al-/Fe-(hydr)oxides–organic carbon associations in Oxisols — From ecosystems to submicron scales
title_fullStr Al-/Fe-(hydr)oxides–organic carbon associations in Oxisols — From ecosystems to submicron scales
title_full_unstemmed Al-/Fe-(hydr)oxides–organic carbon associations in Oxisols — From ecosystems to submicron scales
title_sort Al-/Fe-(hydr)oxides–organic carbon associations in Oxisols — From ecosystems to submicron scales
author Souza, Ivan F.
author_facet Souza, Ivan F.
Archanjo, Bráulio S.
Hurtarte, Luis C.C.
Oliveros, Martin E.
Gouvea, Cristol P.
Lidizio, Leandro R.
Achete, Carlos A.
Schaefer, Carlos E.R.
Silva, Ivo R.
author_role author
author2 Archanjo, Bráulio S.
Hurtarte, Luis C.C.
Oliveros, Martin E.
Gouvea, Cristol P.
Lidizio, Leandro R.
Achete, Carlos A.
Schaefer, Carlos E.R.
Silva, Ivo R.
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Souza, Ivan F.
Archanjo, Bráulio S.
Hurtarte, Luis C.C.
Oliveros, Martin E.
Gouvea, Cristol P.
Lidizio, Leandro R.
Achete, Carlos A.
Schaefer, Carlos E.R.
Silva, Ivo R.
dc.subject.pt-BR.fl_str_mv Al-/Fe-(hydr)oxides
Carbon
Oxisols
Ferralsols
Subtropics
Tropics
topic Al-/Fe-(hydr)oxides
Carbon
Oxisols
Ferralsols
Subtropics
Tropics
description Al-/Fe(hydr)oxides accumulation upon weathering favors soil organic carbon (SOC) protection into mineral-organic associations (MOAs). Paradoxically, tropical ecosystems on highly weathered soils are characterized by high turnover rates of SOC. Our objective was to propose an explanation for such apparent contradiction by inferring the chemical composition of MOAs in Oxisols. To this end, we compiled a large data set from 43 published articles providing chemical and physical properties of 179 Oxisols/Ferralsols and their SOC content in the A horizon. Thermal analysis (TA) coupled to evolved gas detection (EGD) was used to assess mineral dehydroxylation and SOC oxidation in two soils with contrasting SOC content. Scanning transmission electron microscopy (STEM) was used to probe MOAs within the soil fraction < 53 μm. At large scales, SOC content was strongly correlated to Al extractable by both ammonium oxalate (AO) (r = 0.71) and dithionite-citrate-bicarbonate (DCB) (r = 0.41). Weaker, but significant correlations occurred for SOC against Fe-AO and Fe-DCB (r = 0.38, and r = 014, respectively). At micro-scale, SOC also was found associated to Al-/Fe-(hydr)oxides, as inferred from the STEM imaging. TA-EGD indicated that with increasing SOC content, proportionally more organic matter was oxidized following the dehydroxylation of Al-/Fe-(hydr)oxides at temperatures < 400 °C. Within the first 20 cm of the topsoil of the Oxisols included in our data set, Al-AO explained 62% of the total variation in SOC. However, while SOC content varied from 0.8 up to 145.8 g kg− 1 soil, Al-AO varied between 0.2 and 15.3 g kg− 1 soil. From the perspective of mineral control on SOC retention, reactive species of Al-(hydr)oxides should interact with a disproportionally large amount of organic matter. Because mineral protection is seemingly reduced upon increasing C content in MOAs, SOC in Oxisols may be more vulnerable to environmental changes than currently recognized.
publishDate 2017
dc.date.issued.fl_str_mv 2017-07
dc.date.accessioned.fl_str_mv 2018-08-23T13:45:02Z
dc.date.available.fl_str_mv 2018-08-23T13:45:02Z
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dc.identifier.uri.fl_str_mv https://doi.org/10.1016/j.catena.2017.02.017
http://www.locus.ufv.br/handle/123456789/21385
dc.identifier.issn.none.fl_str_mv 0341-8162
identifier_str_mv 0341-8162
url https://doi.org/10.1016/j.catena.2017.02.017
http://www.locus.ufv.br/handle/123456789/21385
dc.language.iso.fl_str_mv eng
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dc.relation.ispartofseries.pt-BR.fl_str_mv volume 154, páginas 63-72, julho 2017
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