Influence of land use on the microbiological properties of urban soils

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Edafoloxía e Química Agrícolagl
dc.contributor.affiliationUniversidade de Santiago de Compostela. Instituto Interdisciplinar de Tecnoloxías Ambientais (CRETUS)gl
dc.contributor.authorGómez-Brandón, Maria
dc.contributor.authorHerbón Allo, Cecilia
dc.contributor.authorProbst, Maraike
dc.contributor.authorFornasier, Favio
dc.contributor.authorBarral Silva, María Teresa
dc.date.accessioned2022-08-10T08:45:19Z
dc.date.available2022-08-10T08:45:19Z
dc.date.issued2022
dc.description.abstractAdvancing towards sustainable cities needs a better understanding of all components of urban ecosystems, including soils, but the biological component of urban soils remains poorly studied compared to natural and agricultural soils. With the objective of advancing knowledge in this aspect, we studied the microbiological properties in 61 soils of the city of Santiago de Compostela (NW Spain), under several land uses (urban grassland, urban forest, urban garden, and periurban arable land). We determined thirteen extracellular enzymatic activities as a proxy of microbial community functioning, along with measures of microbial activity (basal respiration), microbial abundance (DNA extraction and real-time PCR), and the composition of microbial communities (Illumina MiSeq sequencing on 16S rRNA and ITS marker regions). Results showed a high variability in all of the microbiological variables among soils, reflecting the typical spatial heterogeneity of urban soils. Respiration and enzymatic activities were highly correlated to soil organic matter contents but not affected by land use within the city, with the exception of alkaline phosphomonoesterase activity, which was higher in urban garden soils and correlated positively to pH and availability of phosphorus and nitrogen. Unlike fungal abundance, we recorded a higher bacterial abundance in the urban grasslands than in the other land uses. While the composition of bacterial communities was structured in a more homogeneous, land use-dependent manner (33% variance, pAdonis = 0.001), the respective fungal communities were more heterogeneous and less influenced by group-dependent characteristics (18%, pAdonis = 0.001). Soil pH had a larger influence on the bacterial community composition (28% variance) compared to the fungal composition (8.5% variance). Overall, these findings provide evidence that the typically high soil heterogeneity of urban ecosystems is the main driving force for the urban soil microbiome, with soil organic matter determining largely microbial activitygl
dc.description.peerreviewedSIgl
dc.description.sponsorshipDr. Paradelo and Dr. Gómez-Brandón thank the Spanish State Agency for Research (AEI) for their Ramón y Cajal grants RYC-2016-19286 and RYC-2016-21231, funded by MCIN/AEI/10.13039/501100011033 and by “ESF Investing in your future”. This research has been funded by the Xunta de Galicia regional government (grant number ED431F 2018/04)gl
dc.identifier.citationApplied Soil Ecology 175 (2022) 104452gl
dc.identifier.doi10.1016/j.apsoil.2022.104452
dc.identifier.essn0929-1393/
dc.identifier.urihttp://hdl.handle.net/10347/29045
dc.language.isoenggl
dc.publisherElseviergl
dc.relation.publisherversionhttps://doi.org/10.1016/j.apsoil.2022.104452gl
dc.rights©2022 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by- nc-nd/4.0/)gl
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional
dc.rights.accessRightsopen accessgl
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectUrban ecosystemsgl
dc.subjectEnzymatic activitiesgl
dc.subjectMicrobial activitygl
dc.subjectMicrobial communitiesgl
dc.subjectSoil healthgl
dc.titleInfluence of land use on the microbiological properties of urban soilsgl
dc.typejournal articlegl
dc.type.hasVersionVoRgl
dspace.entity.typePublication
relation.isAuthorOfPublication5af89317-a84d-435c-b931-f18288d12a04
relation.isAuthorOfPublication.latestForDiscovery5af89317-a84d-435c-b931-f18288d12a04

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