Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/11126
Title: Molecular sequence analysis of prokaryotic diversity in the middle and outer sections of the Portuguese estuary Ria de Aveiro
Author: Henriques, I. S.
Almeida, A.
Cunha, A.
Correia, A.
Keywords: 16S rDNA clone library
Estuarine bacterioplankton
Phylogenetic diversity
Metabolic activity
Issue Date: Aug-2004
Publisher: Wiley-Blackwell
Abstract: Construction of 16S rDNA libraries was undertaken to examine the structure of free-living bacterial communities in the estuarine system Ria de Aveiro, Portugal. Samples were collected in April 2002, from two sites representing marine (station N1) and brackish (station I6) water zones. Clones were characterized by RFLP patterns and sequence analysis of representative clones revealed that both libraries were clearly dominated by α-proteobacteria, followed by γ-proteobacteria and β-proteobacteria. Clones affiliated with the δ-proteobacteria, Verrucomicrobia, Bacteroidetes and Actinobacteria were exclusive of station I6 and sequences related to the Firmicutes were only found in station N1. Sequences retrieved are included in only a few major bacterial divisions and in general, shared a high degree of homology with sequences deposited in nucleotide databases, and recovered from aquatic environments of diverse geographic regions. Differences between the two sites may reflect adaptation to different environmental conditions, especially salinity. The pattern of prokaryotic diversity is comparable to other coastal and estuarine environments previously studied.
Peer review: yes
URI: http://hdl.handle.net/10773/11126
DOI: 10.1016/j.femsec.2004.04.003
ISSN: 0168-6496
Appears in Collections:DBio - Artigos
PT Mar - Artigos

Files in This Item:
File Description SizeFormat 
Molecular sequence analysis of prokaryotic diversity.pdf236.79 kBAdobe PDFrestrictedAccess


FacebookTwitterLinkedIn
Formato BibTex MendeleyEndnote Degois 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.