The ecology of Cytophaga-Flavobacteria in aquatic environments.

By David L. Kirchman. FEMS Microbiology Ecology, 2002

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Citations in the corpus

Seasonal changes in the taxonomic composition of bacterioplankton in a coastal oligotrophic system (2003, result): “The relative importance of CFB in Blanes Bay, in turn, agrees with results obtained with FISH in a variety of systems and is consistent with the finding that many clone libraries were biased against this important marine bacterial group (Kirchman 2002).”
Interactions between marine snow and heterotrophic bacteria: aggregate formation and microbial dynamics (2006, background): “Based on their behaviour, 3 functional types of bacteria have been described (Rieman et al. 2000, Kirchman 2002, Grossart et al. 2005): (1) bacteria that specialize in colonizing particles (‘particle specialists’); (2) free-living bacteria; and (3) bacte- © Inter-Research 2006 ·…”
Ecology of marine Bacteroidetes: a comparative genomics approach (2013, background): “Members of the phylum Bacteroidetes are the most abundant group of bacteria in the ocean after Proteobacteria and Cyanobacteria (Glöckner et al., 1999; Kirchman, 2002; Amaral-Zettler et al., 2010).”
An introduction to the biogeography of aquatic microbes (2005, background): “Members of other groups such as CytophagaFlavobacteria are abundant in both freshwater and marine systems (Kirchman 2002).”
Microbial Surface Colonization and Biofilm Development in Marine Environments (2015, background): “While the sinking of the particles into deep water will decrease the physiological activity of the particle-associated microorganisms (200), the hydrolytic activities of the secreted extracellular enzymes may be retained (to a large extent), and thus, the resident free-living microorganisms may have”
Temperatures beyond the community optimum promote the dominance of heat-adapted, fast growing and stress resistant bacteria in alpine soils (2020, background): “Mucilaginibacter and Cytophaga play an important role in mineralizing organic matter, as they are able to degrade polysaccharides such as cellulose and chitin (Kirchman, 2002; Nissinen et al., 2012; �Stursov�a et al., 2012).”
Contribution of major bacterial groups to bacterial biomass production (thymidine and leucine incorporation) in the Delaware estuary (2003, positive): “Kirchman 2000b; Kirchman 2002), whereas beta-proteobacteria appear to be the dominant group in freshwater systems (Pernthaler et al. 1998; Methe and Zehr 1999).”
Environmental and Gut Bacteroidetes: The Food Connection (2011, background): “Bacteroidetes are increasingly recognized as an important compartment of the bacterioplankton in marine environments (Jooste and Hugo, 1999; Kirchman, 2002), especially in pelagic oceans.”
Abundance and activity of major groups of prokaryotic plankton in the coastal North Sea during spring and summer (2006, background): “Members of the Bacteroidetes are chemo-organotrophic, known for their capacity to degrade complex carbohydrates such as pectin, cellulose and chitin (Reichenbach & Dworkin 1991, Cottrell & Kirchman 2000, Kirchman 2002).”
Single-cell analysis of bacterial growth, cell size, and community structure in the Delaware estuary (2004, background): “Regardless of the limiting factors, growth rates appear to vary greatly within and between the major phylogenetic groups of bacteria found in aquatic systems (Kirchman 2002, Cottrell & Kirchman 2003).”
Spatio-temporal patterns of bacterioplankton production and community composition related to phytoplankton composition and protistan bacterivory in a dam reservoir (2008, background): “Moreover, the broad bacterioplankton groups distinguished, such as Cytophaga/Flavobacterium/Bacteroidetes and Actinobacteria, represent large and metabolically very diverse groups (e.g. Kirchman 2002, Hahn & Pöckl 2005).”