1997
DOI: 10.3354/meps150275
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Widespread Archaea and novel Bacteria from the deep sea as shown by 16S rRNA gene sequences

Abstract: ABSTRACT. Marine microbial diversity is important yet poorly-known, due to low culturability and undersampling. However, 16s rRNA gene sequences cloned directly from biomass allow us to know what microbial types are present, irrespective of culturing, and to create probes suitable for biodiversity studies. Many sequences are needed for good probe design. Here we report on sequences from 57 deep sea clones, obtained by the polymerase chain reaction with 'universal' primers, from 500 m and 3000 m depths in the n… Show more

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Cited by 230 publications
(224 citation statements)
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“…This is the first time group III is reported as dominating an archaeal assemblage. Group III Euryarchaeota were first identified in the Northeast Pacific (Fuhrman and Davis 1997) and was later detected in different parts of the Mediterranean Sea (Massana et al, 2000;Martin-Cuadrado et al, 2007, the South Atlantic (Martin-Cuadrado et al, 2007;Ló pez-García et al, 2001) and in the North Pacific Ocean . However, group III is usually rarely represented in marine ecosystems, in which MGI Crenarchaeota and group II Euryarchaeota are the most abundant groups (Massana et al, 2000).…”
Section: Discussionmentioning
confidence: 99%
“…This is the first time group III is reported as dominating an archaeal assemblage. Group III Euryarchaeota were first identified in the Northeast Pacific (Fuhrman and Davis 1997) and was later detected in different parts of the Mediterranean Sea (Massana et al, 2000;Martin-Cuadrado et al, 2007, the South Atlantic (Martin-Cuadrado et al, 2007;Ló pez-García et al, 2001) and in the North Pacific Ocean . However, group III is usually rarely represented in marine ecosystems, in which MGI Crenarchaeota and group II Euryarchaeota are the most abundant groups (Massana et al, 2000).…”
Section: Discussionmentioning
confidence: 99%
“…Genome fragments from Group III Euryarchaeota Euryarchaeota Group III was first identified from environmental 16S rRNA gene libraries by Fuhrman and Davis (1997) in samples retrieved from the Northeast Pacific at 500 and 300 m depth, and was later detected at 941 m depth in the Alboran Sea (Mediterranean) (Massana et al, 2000) and at 3000 m depth in the Antarctic Polar Front (Ló pez-García et al, 2001), suggesting that they were specific inhabitants of the deep ocean. Group III members were also detected in metagenomic libraries throughout the ALOHA water column in the Pacific, although at lower frequencies in surface waters .…”
Section: Metabolic Clues From Group II Euryarchaeota Genome Fragmentsmentioning
confidence: 99%
“…Group II Euryarchaeota usually appear to be relatively more abundant in surface waters compared with Thaumarchaeota (Karner et al, 2001;Ghai et al, 2010), but they may be abundant in deep-sea waters as well, reaching in some oceanic regions even higher proportions than Thaumarchaeota (Martín-Cuadrado et al, 2008). The much more enigmatic group III Euryarchaeota have been almost exclusively detected in deep-sea plankton, and are found in general in lower abundance than Thaumarchaeota and group II Euryarchaeota (Fuhrman and Davis, 1997;Martín-Cuadrado et al, 2008).…”
Section: Introductionmentioning
confidence: 98%
“…The other two groups of marine planktonic archaea, groups II and III are phylogenetically related and branch as sister-group of the Thermoplasmatales within the Euryarchaeota in 16S rDNA phylogenetic trees (DeLong, 1992;Fuhrman and Davis, 1997). In contrast with Thaumarchaeota, these euryarchaeotal groups lack any cultured representative and their metabolic capabilities remain unknown, except for the indication of a possible phototrophic metabolism in group II archaea from surface waters .…”
Section: Introductionmentioning
confidence: 99%