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Emissions from Paraná-Etendeka Magmatic Province: evaluating the silicic and thermogenic gases

Detalhes bibliográficos
Ano de defesa: 2024
Autor(a) principal: Esteves, Melina Cristina Borges
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Tese
Tipo de acesso: Acesso aberto
Idioma: eng
Instituição de defesa: Biblioteca Digitais de Teses e Dissertações da USP
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: https://www.teses.usp.br/teses/disponiveis/44/44143/tde-03102024-104246/
Resumo: Brazil hosts one of the world\'s most significant Continental Flood Basalts (CFBs), the Paraná-Etendeka Magmatic Province (PMP), associated with the breakup of the Gondwana Supercontinent and the opening of the Atlantic Ocean. The temporal coincidence between the emplacement of CFBs and global environmental changes emphasizes the potential role that volcanic emissions can exert on atmospheric composition, potentially leading to significant climate and ecosystem disturbances. Although the role of volcanic activity is uncontroversial, the limited data on PMPs magmatic volatiles, especially the silicic magmatism, have made it challenging to assess the potential environmental impacts associated. Additionally, the severity of the environmental disturbance during LIP events may also lie directly on the composition of the gases generated in their respective volcanic basins. Here we bridge these two gaps by first estimating the original volatile budgets of the high-Ti silicic rocks using melt inclusions (MIs) entrapped in plagioclase macrocrysts and the halogen signatures of apatite crystals and second investigating the thermal degassing of sedimentary samples from the Amazonas (CAMP) and Paraná (PMP) Basins. The analyzed MIs bear pre- entrapment crystals, daughter crystals, and fluid-bearing shrinkage bubbles, and they are characterized by silica-rich compositions (69 to 74 SiO2 wt%, on a dry basis), with low Cl and S (up to 363 and 314 ppm, respectively). Apatite crystals are fluorapatite, with consistently high fluorine (F>3.5 wt%) but low chlorine contents (Cl<2000 ppm). Using thermodynamically constrained equations we estimated the exchange reactions that control volatile partitioning, and approximated halogen contents of the equilibrium melt (F ~2800, Cl ~1400 ppm, and H2O ~0.5 wt%). Forward models using the aforementioned data as input closely reproduce apatite compositional trends, allowing insights into the depth of magma storage (c.a. 2 kbar) based on fluid/melt Cl partitioning and on Cl/H2O of equilibrium melt. The depolymerizing nature of F combined with high Rheological Agpaitic Indexes calculated from whole rock data imply an effusive eruptive style, with a passive degassing of F as high as 6.5 Gt, at least 2.1 Gt of Cl, and ~0.5 Gt of S. Experiments reveal significant geochemical and mineralogical alterations, with synthetic fluid inclusions indicating the release of volatiles such as CO2, CH4, N2, H2S, and H2O primarily through decarbonation, dehydration, and cracking of organic matter. Isotopic analysis shows a shift in 13C values, highlighting the impact of thermal processes on isotopic fractionation. Metamorphic reactions and associated fluids are treated to estimate basin-scale devolatilization. Even under conservative degassing effectiveness, the upscaling of our experimental results indicates the generation of 3200 Gt C in the Paraná- Etendeka Province and 14200 Gt C in the CAMP. We emphasize that factors beyond organic matter abundance, such as their quality, gas speciation, and production potential, would have controlled the volume of thermogenic gasses associated with the emplacement of the studied LIPs. The effects of the volcanic-related halogen are likely local due to rapid removal from the atmosphere through rainfall. Additionally, the absence of hydrothermal vent complexes in the PMP suggests that methane generated during metamorphism may have been stored within the geological formations rather than released into the atmosphere, both factors probably contribute to the lack of a significant global paleoenvironmental event linked to Paraná-Etendeka Province.
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spelling Emissions from Paraná-Etendeka Magmatic Province: evaluating the silicic and thermogenic gasesEmissões da Província Magmática Paraná-Etendeka: avaliando os gases silícicos e termogênicosFluid inclusionMelt inclusionnão disponívelParaná-Etendeka Magmatic ProvinceSilic gasesThermogenic gasesBrazil hosts one of the world\'s most significant Continental Flood Basalts (CFBs), the Paraná-Etendeka Magmatic Province (PMP), associated with the breakup of the Gondwana Supercontinent and the opening of the Atlantic Ocean. The temporal coincidence between the emplacement of CFBs and global environmental changes emphasizes the potential role that volcanic emissions can exert on atmospheric composition, potentially leading to significant climate and ecosystem disturbances. Although the role of volcanic activity is uncontroversial, the limited data on PMPs magmatic volatiles, especially the silicic magmatism, have made it challenging to assess the potential environmental impacts associated. Additionally, the severity of the environmental disturbance during LIP events may also lie directly on the composition of the gases generated in their respective volcanic basins. Here we bridge these two gaps by first estimating the original volatile budgets of the high-Ti silicic rocks using melt inclusions (MIs) entrapped in plagioclase macrocrysts and the halogen signatures of apatite crystals and second investigating the thermal degassing of sedimentary samples from the Amazonas (CAMP) and Paraná (PMP) Basins. The analyzed MIs bear pre- entrapment crystals, daughter crystals, and fluid-bearing shrinkage bubbles, and they are characterized by silica-rich compositions (69 to 74 SiO2 wt%, on a dry basis), with low Cl and S (up to 363 and 314 ppm, respectively). Apatite crystals are fluorapatite, with consistently high fluorine (F>3.5 wt%) but low chlorine contents (Cl<2000 ppm). Using thermodynamically constrained equations we estimated the exchange reactions that control volatile partitioning, and approximated halogen contents of the equilibrium melt (F ~2800, Cl ~1400 ppm, and H2O ~0.5 wt%). Forward models using the aforementioned data as input closely reproduce apatite compositional trends, allowing insights into the depth of magma storage (c.a. 2 kbar) based on fluid/melt Cl partitioning and on Cl/H2O of equilibrium melt. The depolymerizing nature of F combined with high Rheological Agpaitic Indexes calculated from whole rock data imply an effusive eruptive style, with a passive degassing of F as high as 6.5 Gt, at least 2.1 Gt of Cl, and ~0.5 Gt of S. Experiments reveal significant geochemical and mineralogical alterations, with synthetic fluid inclusions indicating the release of volatiles such as CO2, CH4, N2, H2S, and H2O primarily through decarbonation, dehydration, and cracking of organic matter. Isotopic analysis shows a shift in 13C values, highlighting the impact of thermal processes on isotopic fractionation. Metamorphic reactions and associated fluids are treated to estimate basin-scale devolatilization. Even under conservative degassing effectiveness, the upscaling of our experimental results indicates the generation of 3200 Gt C in the Paraná- Etendeka Province and 14200 Gt C in the CAMP. We emphasize that factors beyond organic matter abundance, such as their quality, gas speciation, and production potential, would have controlled the volume of thermogenic gasses associated with the emplacement of the studied LIPs. The effects of the volcanic-related halogen are likely local due to rapid removal from the atmosphere through rainfall. Additionally, the absence of hydrothermal vent complexes in the PMP suggests that methane generated during metamorphism may have been stored within the geological formations rather than released into the atmosphere, both factors probably contribute to the lack of a significant global paleoenvironmental event linked to Paraná-Etendeka Province.O Brasil abriga um dos mais expressivos derrames basálticos continentais (CFB) do mundo, a Província Magmática Paraná-Etendeka (PMP), associada à fragmentação do Supercontinente Gondwana e à abertura do Oceano Atlântico. A coincidência temporal entre a colocaçãodos CFBs e as mudanças ambientais globais enfatiza o papel que as emissões vulcânicas podem exercer na composição atmosférica, conduzindo a perturbações climáticas e ecossistémicas significativas. Embora o papel da atividade vulcânica seja incontroverso, os dados limitados sobre os voláteis magmáticos da PMP, especialmente o magmatismo silícico, tornaram difícil avaliar os potenciais impactos ambientais associados. Além disso, a gravidade da perturbação ambiental durante esses eventos também pode estar diretamente ligada à composição dos gases gerados nas suas respectivas bacias vulcânicas. Este trabalho preenche essas duas lacunas primeiro estimando os voláteis originais das rochas silícicas com alto teor de Ti usando inclusões de fundido (MIs) aprisionadas em macrocristais de plagioclásio e as assinaturas de halogênio de cristais de apatita e também investigando a desgaseificação térmica de amostras sedimentares das bacias do Amazonas (CAMP) e Paraná (PMP). As MIs analisadas apresentam cristais pré-aprisionados, cristais filhos e bolhas contendo fluido, e são caracterizadas por composições ricas em sílica (69 a 74% wt% SiO2, em base seca), com baixo Cl e S (363 e 314 ppm, respectivamente). Os cristais de apatita são fluorapatita, com flúor consistentemente alto (F>3,5% wt%), mas baixo teor de cloro (Cl<2.000 ppm). Usando equações termodinamicamente restritas, estimamos as reações de troca que controlam a partição volátil e aproximamos o conteúdo de halogênio do fundido em equilíbrio (F ~ 2.800, Cl ~ 1.400 ppm e H2O ~ 0,5% wt%). Modelos usando os dados acima mencionados reproduzem as tendências de composição da apatita, permitindo estimar a profundidade de armazenamento do magma (~ 2 kbar com base na partição de Cl fluido/fundido e em Cl/H2O do fundido de equilíbrio). A natureza despolimerizante do F combinada com altos índices reológicos Agpaíticos calculados a partir de dados de rocha total implicam um estilo eruptivo efusivo, com uma desgaseificação passiva de F de no máximo 6,5 Gt, pelo menos 2,1 Gt de Cl e ~0,5 Gt de S. Experimentos revelam alterações geoquímicas e mineralógicas significativas, com inclusões fluidas sintéticas indicando a liberação de voláteis como CO2, CH4, N2, H2S e H2O principalmente por meio de descarbonatação, desidratação e craqueamento de matéria orgânica. A análise isotópica mostra uma mudança nos valores de 13C, destacando o impacto dos processos térmicos no fracionamento isotópico. Reações metamórficas e fluidos associados são tratados para estimar a desgaseificação em escala de bacia. Mesmo sob uma eficácia conservadora de desgaseificação, os resultados experimentais indicam a geração de 3.200 Gt C na Província Paraná-Etendeka e 14.200 Gt C na CAMP. Ressaltamos que fatores além da abundância de matéria orgânica, como qualidade, especiação de gases e potencial de produção, teriam controlado o volume de gases termogênicos associados à colocação das Províncias estudadas. Os efeitos do halogênio relacionado ao magmatismo são provavelmente locais devido à rápida remoção através das chuvas. Além disso, a ausência de vents na PMP sugere que o metano gerado durante o metamorfismo pode ter sido armazenado em vez de liberado na atmosfera, ambos os fatores provavelmente contribuem para a inobservância de um evento paleoambiental global significativo ligado à Província Paraná-Etendeka.Biblioteca Digitais de Teses e Dissertações da USPAlves, AdrianaEsteves, Melina Cristina Borges2024-08-09info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisapplication/pdfhttps://www.teses.usp.br/teses/disponiveis/44/44143/tde-03102024-104246/reponame:Biblioteca Digital de Teses e Dissertações da USPinstname:Universidade de São Paulo (USP)instacron:USPReter o conteúdo por motivos de patente, publicação e/ou direitos autoriais.info:eu-repo/semantics/openAccesseng2024-10-03T14:01:02Zoai:teses.usp.br:tde-03102024-104246Biblioteca Digital de Teses e Dissertaçõeshttp://www.teses.usp.br/PUBhttp://www.teses.usp.br/cgi-bin/mtd2br.plvirginia@if.usp.br|| atendimento@aguia.usp.br||virginia@if.usp.bropendoar:27212024-10-03T14:01:02Biblioteca Digital de Teses e Dissertações da USP - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Emissions from Paraná-Etendeka Magmatic Province: evaluating the silicic and thermogenic gases
Emissões da Província Magmática Paraná-Etendeka: avaliando os gases silícicos e termogênicos
title Emissions from Paraná-Etendeka Magmatic Province: evaluating the silicic and thermogenic gases
spellingShingle Emissions from Paraná-Etendeka Magmatic Province: evaluating the silicic and thermogenic gases
Esteves, Melina Cristina Borges
Fluid inclusion
Melt inclusion
não disponível
Paraná-Etendeka Magmatic Province
Silic gases
Thermogenic gases
title_short Emissions from Paraná-Etendeka Magmatic Province: evaluating the silicic and thermogenic gases
title_full Emissions from Paraná-Etendeka Magmatic Province: evaluating the silicic and thermogenic gases
title_fullStr Emissions from Paraná-Etendeka Magmatic Province: evaluating the silicic and thermogenic gases
title_full_unstemmed Emissions from Paraná-Etendeka Magmatic Province: evaluating the silicic and thermogenic gases
title_sort Emissions from Paraná-Etendeka Magmatic Province: evaluating the silicic and thermogenic gases
author Esteves, Melina Cristina Borges
author_facet Esteves, Melina Cristina Borges
author_role author
dc.contributor.none.fl_str_mv Alves, Adriana
dc.contributor.author.fl_str_mv Esteves, Melina Cristina Borges
dc.subject.por.fl_str_mv Fluid inclusion
Melt inclusion
não disponível
Paraná-Etendeka Magmatic Province
Silic gases
Thermogenic gases
topic Fluid inclusion
Melt inclusion
não disponível
Paraná-Etendeka Magmatic Province
Silic gases
Thermogenic gases
description Brazil hosts one of the world\'s most significant Continental Flood Basalts (CFBs), the Paraná-Etendeka Magmatic Province (PMP), associated with the breakup of the Gondwana Supercontinent and the opening of the Atlantic Ocean. The temporal coincidence between the emplacement of CFBs and global environmental changes emphasizes the potential role that volcanic emissions can exert on atmospheric composition, potentially leading to significant climate and ecosystem disturbances. Although the role of volcanic activity is uncontroversial, the limited data on PMPs magmatic volatiles, especially the silicic magmatism, have made it challenging to assess the potential environmental impacts associated. Additionally, the severity of the environmental disturbance during LIP events may also lie directly on the composition of the gases generated in their respective volcanic basins. Here we bridge these two gaps by first estimating the original volatile budgets of the high-Ti silicic rocks using melt inclusions (MIs) entrapped in plagioclase macrocrysts and the halogen signatures of apatite crystals and second investigating the thermal degassing of sedimentary samples from the Amazonas (CAMP) and Paraná (PMP) Basins. The analyzed MIs bear pre- entrapment crystals, daughter crystals, and fluid-bearing shrinkage bubbles, and they are characterized by silica-rich compositions (69 to 74 SiO2 wt%, on a dry basis), with low Cl and S (up to 363 and 314 ppm, respectively). Apatite crystals are fluorapatite, with consistently high fluorine (F>3.5 wt%) but low chlorine contents (Cl<2000 ppm). Using thermodynamically constrained equations we estimated the exchange reactions that control volatile partitioning, and approximated halogen contents of the equilibrium melt (F ~2800, Cl ~1400 ppm, and H2O ~0.5 wt%). Forward models using the aforementioned data as input closely reproduce apatite compositional trends, allowing insights into the depth of magma storage (c.a. 2 kbar) based on fluid/melt Cl partitioning and on Cl/H2O of equilibrium melt. The depolymerizing nature of F combined with high Rheological Agpaitic Indexes calculated from whole rock data imply an effusive eruptive style, with a passive degassing of F as high as 6.5 Gt, at least 2.1 Gt of Cl, and ~0.5 Gt of S. Experiments reveal significant geochemical and mineralogical alterations, with synthetic fluid inclusions indicating the release of volatiles such as CO2, CH4, N2, H2S, and H2O primarily through decarbonation, dehydration, and cracking of organic matter. Isotopic analysis shows a shift in 13C values, highlighting the impact of thermal processes on isotopic fractionation. Metamorphic reactions and associated fluids are treated to estimate basin-scale devolatilization. Even under conservative degassing effectiveness, the upscaling of our experimental results indicates the generation of 3200 Gt C in the Paraná- Etendeka Province and 14200 Gt C in the CAMP. We emphasize that factors beyond organic matter abundance, such as their quality, gas speciation, and production potential, would have controlled the volume of thermogenic gasses associated with the emplacement of the studied LIPs. The effects of the volcanic-related halogen are likely local due to rapid removal from the atmosphere through rainfall. Additionally, the absence of hydrothermal vent complexes in the PMP suggests that methane generated during metamorphism may have been stored within the geological formations rather than released into the atmosphere, both factors probably contribute to the lack of a significant global paleoenvironmental event linked to Paraná-Etendeka Province.
publishDate 2024
dc.date.none.fl_str_mv 2024-08-09
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.teses.usp.br/teses/disponiveis/44/44143/tde-03102024-104246/
url https://www.teses.usp.br/teses/disponiveis/44/44143/tde-03102024-104246/
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv
dc.rights.driver.fl_str_mv Reter o conteúdo por motivos de patente, publicação e/ou direitos autoriais.
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Reter o conteúdo por motivos de patente, publicação e/ou direitos autoriais.
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.coverage.none.fl_str_mv
dc.publisher.none.fl_str_mv Biblioteca Digitais de Teses e Dissertações da USP
publisher.none.fl_str_mv Biblioteca Digitais de Teses e Dissertações da USP
dc.source.none.fl_str_mv
reponame:Biblioteca Digital de Teses e Dissertações da USP
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Biblioteca Digital de Teses e Dissertações da USP
collection Biblioteca Digital de Teses e Dissertações da USP
repository.name.fl_str_mv Biblioteca Digital de Teses e Dissertações da USP - Universidade de São Paulo (USP)
repository.mail.fl_str_mv virginia@if.usp.br|| atendimento@aguia.usp.br||virginia@if.usp.br
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