Unrecognized controls on microbial functioning in Blue Carbon ecosystems: The role of mineral enzyme stabilization and allochthonous substrate supply

Abstract Tidal wetlands are effective carbon sinks, mitigating climate change through the long‐term removal of atmospheric CO2. Studies along surface‐elevation and thus flooding‐frequency gradients in tidal wetlands are often used to understand the effects of accelerated sea‐level rise on carbon seq...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Peter Mueller, Dirk Granse, Stefanie Nolte, Magdalena Weingartner, Stefan Hoth, Kai Jensen
Formato: article
Lenguaje:EN
Publicado: Wiley 2020
Materias:
Acceso en línea:https://doaj.org/article/e67e5762a1794e57854b464b4ce469a1
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:e67e5762a1794e57854b464b4ce469a1
record_format dspace
spelling oai:doaj.org-article:e67e5762a1794e57854b464b4ce469a12021-11-04T13:06:10ZUnrecognized controls on microbial functioning in Blue Carbon ecosystems: The role of mineral enzyme stabilization and allochthonous substrate supply2045-775810.1002/ece3.5962https://doaj.org/article/e67e5762a1794e57854b464b4ce469a12020-01-01T00:00:00Zhttps://doi.org/10.1002/ece3.5962https://doaj.org/toc/2045-7758Abstract Tidal wetlands are effective carbon sinks, mitigating climate change through the long‐term removal of atmospheric CO2. Studies along surface‐elevation and thus flooding‐frequency gradients in tidal wetlands are often used to understand the effects of accelerated sea‐level rise on carbon sequestration, a process that is primarily determined by the balance of primary production and microbial decomposition. It has often been hypothesized that rates of microbial decomposition would increase with elevation and associated increases in soil oxygen availability; however, previous studies yield a wide range of outcomes and equivocal results. Our mechanistic understanding of the elevation–decomposition relationship is limited because most effort has been devoted to understanding the terminal steps of the decomposition process. A few studies assessed microbial exo‐enzyme activities (EEAs) as initial and rate‐limiting steps that often reveal important insight into microbial energy and nutrient constraints. The present study assessed EEAs and microbial abundance along a coastal ecotone stretching a flooding gradient from tidal flat to high marsh in the European Wadden Sea. We found that stabilization of exo‐enzymes to mineral sediments leads to high specific EEAs at low substrate concentrations in frequently flooded, sediment‐rich zones of the studied ecotone. We argue that the high background activity of a mineral‐associated enzyme pool provides a stable decomposition matrix in highly dynamic, frequently flooded zones. Furthermore, we demonstrate that microbial communities are less nutrient limited in frequently flooded zones, where inputs of nutrient‐rich marine organic matter are higher. This was reflected in both increasing exo‐enzymatic carbon versus nutrient acquisition and decreasing fungal versus bacterial abundance with increasing flooding frequency. Our findings thereby suggest two previously unrecognized mechanisms that may contribute to stimulated microbial activity despite decreasing oxygen availability in response to accelerated sea‐level rise.Peter MuellerDirk GranseStefanie NolteMagdalena WeingartnerStefan HothKai JensenWileyarticlecarbon sequestrationexo‐enzymesfungiquantitative PCRIndicator of Reduction in Soilssalt marshEcologyQH540-549.5ENEcology and Evolution, Vol 10, Iss 2, Pp 998-1011 (2020)
institution DOAJ
collection DOAJ
language EN
topic carbon sequestration
exo‐enzymes
fungi
quantitative PCR
Indicator of Reduction in Soils
salt marsh
Ecology
QH540-549.5
spellingShingle carbon sequestration
exo‐enzymes
fungi
quantitative PCR
Indicator of Reduction in Soils
salt marsh
Ecology
QH540-549.5
Peter Mueller
Dirk Granse
Stefanie Nolte
Magdalena Weingartner
Stefan Hoth
Kai Jensen
Unrecognized controls on microbial functioning in Blue Carbon ecosystems: The role of mineral enzyme stabilization and allochthonous substrate supply
description Abstract Tidal wetlands are effective carbon sinks, mitigating climate change through the long‐term removal of atmospheric CO2. Studies along surface‐elevation and thus flooding‐frequency gradients in tidal wetlands are often used to understand the effects of accelerated sea‐level rise on carbon sequestration, a process that is primarily determined by the balance of primary production and microbial decomposition. It has often been hypothesized that rates of microbial decomposition would increase with elevation and associated increases in soil oxygen availability; however, previous studies yield a wide range of outcomes and equivocal results. Our mechanistic understanding of the elevation–decomposition relationship is limited because most effort has been devoted to understanding the terminal steps of the decomposition process. A few studies assessed microbial exo‐enzyme activities (EEAs) as initial and rate‐limiting steps that often reveal important insight into microbial energy and nutrient constraints. The present study assessed EEAs and microbial abundance along a coastal ecotone stretching a flooding gradient from tidal flat to high marsh in the European Wadden Sea. We found that stabilization of exo‐enzymes to mineral sediments leads to high specific EEAs at low substrate concentrations in frequently flooded, sediment‐rich zones of the studied ecotone. We argue that the high background activity of a mineral‐associated enzyme pool provides a stable decomposition matrix in highly dynamic, frequently flooded zones. Furthermore, we demonstrate that microbial communities are less nutrient limited in frequently flooded zones, where inputs of nutrient‐rich marine organic matter are higher. This was reflected in both increasing exo‐enzymatic carbon versus nutrient acquisition and decreasing fungal versus bacterial abundance with increasing flooding frequency. Our findings thereby suggest two previously unrecognized mechanisms that may contribute to stimulated microbial activity despite decreasing oxygen availability in response to accelerated sea‐level rise.
format article
author Peter Mueller
Dirk Granse
Stefanie Nolte
Magdalena Weingartner
Stefan Hoth
Kai Jensen
author_facet Peter Mueller
Dirk Granse
Stefanie Nolte
Magdalena Weingartner
Stefan Hoth
Kai Jensen
author_sort Peter Mueller
title Unrecognized controls on microbial functioning in Blue Carbon ecosystems: The role of mineral enzyme stabilization and allochthonous substrate supply
title_short Unrecognized controls on microbial functioning in Blue Carbon ecosystems: The role of mineral enzyme stabilization and allochthonous substrate supply
title_full Unrecognized controls on microbial functioning in Blue Carbon ecosystems: The role of mineral enzyme stabilization and allochthonous substrate supply
title_fullStr Unrecognized controls on microbial functioning in Blue Carbon ecosystems: The role of mineral enzyme stabilization and allochthonous substrate supply
title_full_unstemmed Unrecognized controls on microbial functioning in Blue Carbon ecosystems: The role of mineral enzyme stabilization and allochthonous substrate supply
title_sort unrecognized controls on microbial functioning in blue carbon ecosystems: the role of mineral enzyme stabilization and allochthonous substrate supply
publisher Wiley
publishDate 2020
url https://doaj.org/article/e67e5762a1794e57854b464b4ce469a1
work_keys_str_mv AT petermueller unrecognizedcontrolsonmicrobialfunctioninginbluecarbonecosystemstheroleofmineralenzymestabilizationandallochthonoussubstratesupply
AT dirkgranse unrecognizedcontrolsonmicrobialfunctioninginbluecarbonecosystemstheroleofmineralenzymestabilizationandallochthonoussubstratesupply
AT stefanienolte unrecognizedcontrolsonmicrobialfunctioninginbluecarbonecosystemstheroleofmineralenzymestabilizationandallochthonoussubstratesupply
AT magdalenaweingartner unrecognizedcontrolsonmicrobialfunctioninginbluecarbonecosystemstheroleofmineralenzymestabilizationandallochthonoussubstratesupply
AT stefanhoth unrecognizedcontrolsonmicrobialfunctioninginbluecarbonecosystemstheroleofmineralenzymestabilizationandallochthonoussubstratesupply
AT kaijensen unrecognizedcontrolsonmicrobialfunctioninginbluecarbonecosystemstheroleofmineralenzymestabilizationandallochthonoussubstratesupply
_version_ 1718444933492244480