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Satellite remote sensing data can be used to model marine microbial metabolite turnover
Sampling ecosystems, even at a local scale, at the temporal and spatial resolution necessary to capture natural variability in microbial communities are prohibitively expensive. We extrapolated marine surface microbial community structure and metabolic potential from 72 16S rRNA amplicon and 8 metag...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4274419/ https://www.ncbi.nlm.nih.gov/pubmed/25072414 http://dx.doi.org/10.1038/ismej.2014.107 |
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author | Larsen, Peter E Scott, Nicole Post, Anton F Field, Dawn Knight, Rob Hamada, Yuki Gilbert, Jack A |
author_facet | Larsen, Peter E Scott, Nicole Post, Anton F Field, Dawn Knight, Rob Hamada, Yuki Gilbert, Jack A |
author_sort | Larsen, Peter E |
collection | PubMed |
description | Sampling ecosystems, even at a local scale, at the temporal and spatial resolution necessary to capture natural variability in microbial communities are prohibitively expensive. We extrapolated marine surface microbial community structure and metabolic potential from 72 16S rRNA amplicon and 8 metagenomic observations using remotely sensed environmental parameters to create a system-scale model of marine microbial metabolism for 5904 grid cells (49 km(2)) in the Western English Chanel, across 3 years of weekly averages. Thirteen environmental variables predicted the relative abundance of 24 bacterial Orders and 1715 unique enzyme-encoding genes that encode turnover of 2893 metabolites. The genes' predicted relative abundance was highly correlated (Pearson Correlation 0.72, P-value <10(−6)) with their observed relative abundance in sequenced metagenomes. Predictions of the relative turnover (synthesis or consumption) of CO(2) were significantly correlated with observed surface CO(2) fugacity. The spatial and temporal variation in the predicted relative abundances of genes coding for cyanase, carbon monoxide and malate dehydrogenase were investigated along with the predicted inter-annual variation in relative consumption or production of ∼3000 metabolites forming six significant temporal clusters. These spatiotemporal distributions could possibly be explained by the co-occurrence of anaerobic and aerobic metabolisms associated with localized plankton blooms or sediment resuspension, which facilitate the presence of anaerobic micro-niches. This predictive model provides a general framework for focusing future sampling and experimental design to relate biogeochemical turnover to microbial ecology. |
format | Online Article Text |
id | pubmed-4274419 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-42744192015-01-01 Satellite remote sensing data can be used to model marine microbial metabolite turnover Larsen, Peter E Scott, Nicole Post, Anton F Field, Dawn Knight, Rob Hamada, Yuki Gilbert, Jack A ISME J Original Article Sampling ecosystems, even at a local scale, at the temporal and spatial resolution necessary to capture natural variability in microbial communities are prohibitively expensive. We extrapolated marine surface microbial community structure and metabolic potential from 72 16S rRNA amplicon and 8 metagenomic observations using remotely sensed environmental parameters to create a system-scale model of marine microbial metabolism for 5904 grid cells (49 km(2)) in the Western English Chanel, across 3 years of weekly averages. Thirteen environmental variables predicted the relative abundance of 24 bacterial Orders and 1715 unique enzyme-encoding genes that encode turnover of 2893 metabolites. The genes' predicted relative abundance was highly correlated (Pearson Correlation 0.72, P-value <10(−6)) with their observed relative abundance in sequenced metagenomes. Predictions of the relative turnover (synthesis or consumption) of CO(2) were significantly correlated with observed surface CO(2) fugacity. The spatial and temporal variation in the predicted relative abundances of genes coding for cyanase, carbon monoxide and malate dehydrogenase were investigated along with the predicted inter-annual variation in relative consumption or production of ∼3000 metabolites forming six significant temporal clusters. These spatiotemporal distributions could possibly be explained by the co-occurrence of anaerobic and aerobic metabolisms associated with localized plankton blooms or sediment resuspension, which facilitate the presence of anaerobic micro-niches. This predictive model provides a general framework for focusing future sampling and experimental design to relate biogeochemical turnover to microbial ecology. Nature Publishing Group 2015-01 2014-07-29 /pmc/articles/PMC4274419/ /pubmed/25072414 http://dx.doi.org/10.1038/ismej.2014.107 Text en Copyright © 2015 International Society for Microbial Ecology http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Original Article Larsen, Peter E Scott, Nicole Post, Anton F Field, Dawn Knight, Rob Hamada, Yuki Gilbert, Jack A Satellite remote sensing data can be used to model marine microbial metabolite turnover |
title | Satellite remote sensing data can be used to model marine microbial metabolite turnover |
title_full | Satellite remote sensing data can be used to model marine microbial metabolite turnover |
title_fullStr | Satellite remote sensing data can be used to model marine microbial metabolite turnover |
title_full_unstemmed | Satellite remote sensing data can be used to model marine microbial metabolite turnover |
title_short | Satellite remote sensing data can be used to model marine microbial metabolite turnover |
title_sort | satellite remote sensing data can be used to model marine microbial metabolite turnover |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4274419/ https://www.ncbi.nlm.nih.gov/pubmed/25072414 http://dx.doi.org/10.1038/ismej.2014.107 |
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