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Short‐term changes in the composition of active marine bacterial assemblages in response to diesel oil pollution

The changes caused by diesel oil pollution in the metabolically active bacterioplankton from an oligotrophic coastal location were analysed in laboratory microcosms (44 l) using 16S ribosomal RNA (16S rRNA) as molecular marker. The aim was to simulate typical hydrocarbon pollution events in a coasta...

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Autores principales: Lanfranconi, Mariana P., Bosch, Rafael, Nogales, Balbina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815773/
https://www.ncbi.nlm.nih.gov/pubmed/21255357
http://dx.doi.org/10.1111/j.1751-7915.2010.00192.x
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author Lanfranconi, Mariana P.
Bosch, Rafael
Nogales, Balbina
author_facet Lanfranconi, Mariana P.
Bosch, Rafael
Nogales, Balbina
author_sort Lanfranconi, Mariana P.
collection PubMed
description The changes caused by diesel oil pollution in the metabolically active bacterioplankton from an oligotrophic coastal location were analysed in laboratory microcosms (44 l) using 16S ribosomal RNA (16S rRNA) as molecular marker. The aim was to simulate typical hydrocarbon pollution events in a coastal area exploited for seasonal touristic activities. The experiment consisted in addition of low amounts of diesel oil without nutrients to seawater collected at different times (winter and summer). Bacterial diversity was analysed by terminal‐restriction fragment length polymorphism (T‐RFLP) profiling of 16S rRNAs after reverse transcription polymerase chain reaction (RT‐PCR), and by generation of 16S rRNA clone libraries in control and diesel‐polluted microcosms. Diesel addition caused a twofold increase in prokaryotic numbers in comparison with controls at the end of the experiment, both in winter and summer microcosms. Bacterioplankton composition, determined by 16S rRNA T‐RFLP data, changed rapidly (within 17 h) in response to treatment. The resulting communities were different in microcosms with water collected in summer and winter. A reduction in diversity (Shannon index, calculated on the basis of T‐RFLP data) was observed only in summer microcosms. This was due to the rapid increase of phylotypes affiliated to the Oceanospirillaceae, not observed in winter microcosms. After diesel treatment there was a reduction in the number of phylotypes related to SAR11, SAR86 and picocyanobacteria, while phylotypes of the Roseobacter clade, and the OMG group seemed to be favoured. Our results show that diesel pollution alone caused profound effects on the bacterioplankton of oligotrophic seawater, and explained many of the differences in diversity reported previously in pristine and polluted sites in this coastal area.
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spelling pubmed-38157732014-02-12 Short‐term changes in the composition of active marine bacterial assemblages in response to diesel oil pollution Lanfranconi, Mariana P. Bosch, Rafael Nogales, Balbina Microb Biotechnol Research Articles The changes caused by diesel oil pollution in the metabolically active bacterioplankton from an oligotrophic coastal location were analysed in laboratory microcosms (44 l) using 16S ribosomal RNA (16S rRNA) as molecular marker. The aim was to simulate typical hydrocarbon pollution events in a coastal area exploited for seasonal touristic activities. The experiment consisted in addition of low amounts of diesel oil without nutrients to seawater collected at different times (winter and summer). Bacterial diversity was analysed by terminal‐restriction fragment length polymorphism (T‐RFLP) profiling of 16S rRNAs after reverse transcription polymerase chain reaction (RT‐PCR), and by generation of 16S rRNA clone libraries in control and diesel‐polluted microcosms. Diesel addition caused a twofold increase in prokaryotic numbers in comparison with controls at the end of the experiment, both in winter and summer microcosms. Bacterioplankton composition, determined by 16S rRNA T‐RFLP data, changed rapidly (within 17 h) in response to treatment. The resulting communities were different in microcosms with water collected in summer and winter. A reduction in diversity (Shannon index, calculated on the basis of T‐RFLP data) was observed only in summer microcosms. This was due to the rapid increase of phylotypes affiliated to the Oceanospirillaceae, not observed in winter microcosms. After diesel treatment there was a reduction in the number of phylotypes related to SAR11, SAR86 and picocyanobacteria, while phylotypes of the Roseobacter clade, and the OMG group seemed to be favoured. Our results show that diesel pollution alone caused profound effects on the bacterioplankton of oligotrophic seawater, and explained many of the differences in diversity reported previously in pristine and polluted sites in this coastal area. Blackwell Publishing Ltd 2010-09 2010-08-19 /pmc/articles/PMC3815773/ /pubmed/21255357 http://dx.doi.org/10.1111/j.1751-7915.2010.00192.x Text en Copyright © 2010 The Author. Journal compilation © 2010 Society for Applied Microbiology and Blackwell Publishing Ltd
spellingShingle Research Articles
Lanfranconi, Mariana P.
Bosch, Rafael
Nogales, Balbina
Short‐term changes in the composition of active marine bacterial assemblages in response to diesel oil pollution
title Short‐term changes in the composition of active marine bacterial assemblages in response to diesel oil pollution
title_full Short‐term changes in the composition of active marine bacterial assemblages in response to diesel oil pollution
title_fullStr Short‐term changes in the composition of active marine bacterial assemblages in response to diesel oil pollution
title_full_unstemmed Short‐term changes in the composition of active marine bacterial assemblages in response to diesel oil pollution
title_short Short‐term changes in the composition of active marine bacterial assemblages in response to diesel oil pollution
title_sort short‐term changes in the composition of active marine bacterial assemblages in response to diesel oil pollution
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815773/
https://www.ncbi.nlm.nih.gov/pubmed/21255357
http://dx.doi.org/10.1111/j.1751-7915.2010.00192.x
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