Literature DB >> 16348743

Effect of protistan grazing on the frequency of dividing cells in bacterioplankton assemblages.

B F Sherr1, E B Sherr, J McDaniel.   

Abstract

Grazing by phagotrophic flagellates and ciliates is a major source of mortality for bacterioplankton in both marine and freshwater systems. Recent studies have demonstrated a positive relationship between clearance rate and prey size for bacterivorous protists. We tested the idea that, by selectively grazing the larger (more actively growing or dividing) cells in a bacterial assemblage, protists control bacterial standing stock abundances by directly cropping bacterial production. Samples of estuarine water were passed through 0.8-mum-pore-size filters (bacteria only) or 20-mum-mesh screens (bacteria and bacterivorous protists) and placed in dialysis tubing suspended in 7 liters of unfiltered water. Changes in total bacterial biovolume per milliliter (bacterial biomass), frequency of dividing cells (FDC), and average per cell biovolume were followed over a period of 24 h. In three experiments, the FDC increased more rapidly and attained higher values in water passed through 0.8-mum-pore-size filters (average, 5.1 to 8.9%; maximum, 15.5%) compared with FDC values in water passed through 20-mum-mesh screens (average, 2.7 to 5.3%; maximum, 6.7%). Increases in bacterial biomass per milliliter lagged behind increases in FDC by about 4 to 6 h. Grazed bacterial assemblages were characterized by lower total biomasses and smaller average cell sizes compared with those of cells in nongrazed assemblages. We conclude that bacterivorous protists control bacterial standing stock abundances partly by preferentially removing dividing cells. Selective grazing of the more actively growing cells may also explain, in part, the ability of slow-growing cells to persist in bacterioplankton assemblages.

Entities:  

Year:  1992        PMID: 16348743      PMCID: PMC195790          DOI: 10.1128/aem.58.8.2381-2385.1992

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  5 in total

1.  Size-selective grazing on bacteria by natural assemblages of estuarine flagellates and ciliates.

Authors:  J M Gonzalez; E B Sherr; B F Sherr
Journal:  Appl Environ Microbiol       Date:  1990-03       Impact factor: 4.792

2.  Viruses as partners in spring bloom microbial trophodynamics.

Authors:  G Bratbak; M Heldal; S Norland; T F Thingstad
Journal:  Appl Environ Microbiol       Date:  1990-05       Impact factor: 4.792

3.  Frequency of dividing cells as an estimator of bacterial productivity.

Authors:  S Y Newell; R R Christian
Journal:  Appl Environ Microbiol       Date:  1981-07       Impact factor: 4.792

4.  Frequency of dividing cells, a new approach to the determination of bacterial growth rates in aquatic environments.

Authors:  A Hagström; U Larsson; P Hörstedt; S Normark
Journal:  Appl Environ Microbiol       Date:  1979-05       Impact factor: 4.792

5.  Use of nuclepore filters for counting bacteria by fluorescence microscopy.

Authors:  J E Hobbie; R J Daley; S Jasper
Journal:  Appl Environ Microbiol       Date:  1977-05       Impact factor: 4.792

  5 in total
  38 in total

1.  Detritus-dependent development of the microbial community in an experimental system: qualitative analysis by denaturing gradient gel electrophoresis.

Authors:  E J van Hannen; W Mooij; M P van Agterveld; H J Gons; H J Laanbroek
Journal:  Appl Environ Microbiol       Date:  1999-06       Impact factor: 4.792

2.  Bacterivory rate estimates and fraction of active bacterivores in natural protist assemblages from aquatic systems

Authors: 
Journal:  Appl Environ Microbiol       Date:  1999-04       Impact factor: 4.792

3.  Impact of protozoan grazing on bacterial community structure in soil microcosms.

Authors:  Regin Rønn; Allison E McCaig; Bryan S Griffiths; James I Prosser
Journal:  Appl Environ Microbiol       Date:  2002-12       Impact factor: 4.792

4.  The bacterivorous soil flagellate Heteromita globosa reduces bacterial clogging under denitrifying conditions in sand-filled aquifer columns.

Authors:  Richard G Mattison; Hironori Taki; Shigeaki Harayama
Journal:  Appl Environ Microbiol       Date:  2002-09       Impact factor: 4.792

5.  Strain-specific differences in the grazing sensitivities of closely related ultramicrobacteria affiliated with the Polynucleobacter cluster.

Authors:  Jens Boenigk; Peter Stadler; Anneliese Wiedlroither; Martin W Hahn
Journal:  Appl Environ Microbiol       Date:  2004-10       Impact factor: 4.792

6.  Marine bacterial community structure resilience to changes in protist predation under phytoplankton bloom conditions.

Authors:  Federico Baltar; Joakim Palovaara; Fernando Unrein; Philippe Catala; Karel Horňák; Karel Šimek; Dolors Vaqué; Ramon Massana; Josep M Gasol; Jarone Pinhassi
Journal:  ISME J       Date:  2015-08-11       Impact factor: 10.302

7.  High motility reduces grazing mortality of planktonic bacteria.

Authors:  Carsten Matz; Klaus Jürgens
Journal:  Appl Environ Microbiol       Date:  2005-02       Impact factor: 4.792

Review 8.  Fate of heterotrophic microbes in pelagic habitats: focus on populations.

Authors:  Jakob Pernthaler; Rudolf Amann
Journal:  Microbiol Mol Biol Rev       Date:  2005-09       Impact factor: 11.056

9.  Direct and indirect evidence of size-selective grazing on pelagic bacteria by freshwater nanoflagellates.

Authors:  K Simek; T H Chrzanowski
Journal:  Appl Environ Microbiol       Date:  1992-11       Impact factor: 4.792

10.  Prey food quality affects flagellate ingestion rates.

Authors:  S Paul Shannon; Thomas H Chrzanowski; James P Grover
Journal:  Microb Ecol       Date:  2006-12-22       Impact factor: 4.552

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