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  • 1
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    Picoheterotrophs in the Northeast Pacific (2014)
    PANGAEA
    Details
    Publication Date: 2023-03-09
    Keywords: Bottle, Niskin; Date/Time of event; DEPTH, water; Event label; Flow cytometry; Global Ocean Ecosystem Dynamics; GLOBEC; Latitude of event; Longitude of event; NEP-LTOP-CR10-2001-9; NEP-LTOP-CR10-2003-7; NEP-LTOP-CR11-2002-4; NEP-LTOP-CR11-2002-7; NEP-LTOP-CR11-2002-9; NEP-LTOP-CR11-2003-7; NEP-LTOP-CR11-2003-9; NEP-LTOP-CR1-2001-3; NEP-LTOP-CR1-2001-9; NEP-LTOP-CR1-2002-4; NEP-LTOP-CR1-2002-7; NEP-LTOP-CR1-2002-9; NEP-LTOP-CR1-2003-4; NEP-LTOP-CR1-2003-7; NEP-LTOP-CR1-2003-9; NEP-LTOP-CR2-2002-9; NEP-LTOP-CR2-2003-4; NEP-LTOP-CR2-2003-7; NEP-LTOP-CR2-2003-9; NEP-LTOP-CR3-2001-3; NEP-LTOP-CR3-2001-9; NEP-LTOP-CR3-2002-4; NEP-LTOP-CR3-2002-7; NEP-LTOP-CR3-2002-9; NEP-LTOP-CR3-2003-4; NEP-LTOP-CR3-2003-7; NEP-LTOP-CR3-2003-9; NEP-LTOP-CR4-2001-3; NEP-LTOP-CR4-2001-9; NEP-LTOP-CR4-2002-4; NEP-LTOP-CR4-2002-7; NEP-LTOP-CR4-2002-9; NEP-LTOP-CR4-2003-4; NEP-LTOP-CR4-2003-7; NEP-LTOP-CR4-2003-9; NEP-LTOP-CR5-2001-9; NEP-LTOP-CR5-2002-4; NEP-LTOP-CR5-2002-7; NEP-LTOP-CR5-2002-9; NEP-LTOP-CR5-2003-4; NEP-LTOP-CR5-2003-7; NEP-LTOP-CR5-2003-9; NEP-LTOP-CR6-2003-7; NEP-LTOP-CR6-2003-9; NEP-LTOP-CR7-2001-3; NEP-LTOP-CR7-2001-9; NEP-LTOP-CR7-2002-4; NEP-LTOP-CR7-2002-7; NEP-LTOP-CR7-2002-9; NEP-LTOP-CR7-2003-4; NEP-LTOP-CR7-2003-7; NEP-LTOP-CR7-2003-9; NEP-LTOP-CR8-2003-7; NEP-LTOP-CR8-2003-9; NEP-LTOP-CR9-2002-4; NEP-LTOP-CR9-2003-9; NEP-LTOP-CR9a-2001-3; NEP-LTOP-CR9A-2001-9; NEP-LTOP-CR9a-2002-7; NEP-LTOP-CR9a-2002-9; NEP-LTOP-CR9a-2003-4; NEP-LTOP-CR9a-2003-7; NEP-LTOP-FM1-2002-7; NEP-LTOP-FM1-2002-9; NEP-LTOP-FM1-2003-4; NEP-LTOP-FM1-2003-7; NEP-LTOP-FM1-2003-9; NEP-LTOP-FM1a-2003-9; NEP-LTOP-FM3-2001-3; NEP-LTOP-FM3-2001-9; NEP-LTOP-FM3-2002-4; NEP-LTOP-FM3-2002-7; NEP-LTOP-FM3-2002-9; NEP-LTOP-FM3-2003-4; NEP-LTOP-FM3-2003-7; NEP-LTOP-FM3-2003-9; NEP-LTOP-FM4-2001-3; NEP-LTOP-FM4-2001-9; NEP-LTOP-FM4-2002-4; NEP-LTOP-FM4-2002-7; NEP-LTOP-FM4-2002-9; NEP-LTOP-FM4-2003-4; NEP-LTOP-FM4-2003-7; NEP-LTOP-FM4-2003-9; NEP-LTOP-FM5-2001-9; NEP-LTOP-FM5-2002-4; NEP-LTOP-FM5-2002-7; NEP-LTOP-FM5-2002-9; NEP-LTOP-FM5-2003-4; NEP-LTOP-FM5-2003-7; NEP-LTOP-FM5-2003-9; NEP-LTOP-FM6-2002-9; NEP-LTOP-FM6-2003-7; NEP-LTOP-FM6-2003-9; NEP-LTOP-FM7-2001-3; NEP-LTOP-FM7-2001-9; NEP-LTOP-FM7-2002-4; NEP-LTOP-FM7-2002-7; NEP-LTOP-FM7-2002-9; NEP-LTOP-FM7-2003-4; NEP-LTOP-FM7-2003-7; NEP-LTOP-FM7-2003-9; NEP-LTOP-FM8-2001-9; NEP-LTOP-FM8-2002-4; NEP-LTOP-FM8-2002-7; NEP-LTOP-FM8-2002-9; NEP-LTOP-FM8-2003-4; NEP-LTOP-FM8-2003-7; NEP-LTOP-FM8-2003-9; NEP-LTOP-FM9-2001-9; NEP-LTOP-FM9-2002-4; NEP-LTOP-FM9-2002-7; NEP-LTOP-FM9-2002-9; NEP-LTOP-FM9-2003-4; NEP-LTOP-FM9-2003-7; NEP-LTOP-FM9-2003-9; NEP-LTOP-HH1-2001-9; NEP-LTOP-HH1-2002-4; NEP-LTOP-HH1-2002-7; NEP-LTOP-HH1-2002-9; NEP-LTOP-HH1-2003-4; NEP-LTOP-HH1-2003-7; NEP-LTOP-HH1-2003-9; NEP-LTOP-HH15-2003-4; NEP-LTOP-HH2-2001-9; NEP-LTOP-HH2-2002-4; NEP-LTOP-HH2-2002-9; NEP-LTOP-HH2-2003-4; NEP-LTOP-HH2-2003-7; NEP-LTOP-HH2-2003-9; NEP-LTOP-HH3-2001-9; NEP-LTOP-HH3-2002-4; NEP-LTOP-HH3-2002-9; NEP-LTOP-HH3-2003-4; NEP-LTOP-HH3-2003-7; NEP-LTOP-HH3-2003-9; NEP-LTOP-HH4-2001-9; NEP-LTOP-HH4-2002-4; NEP-LTOP-HH4-2002-9; NEP-LTOP-HH4-2003-4; NEP-LTOP-HH4-2003-7; NEP-LTOP-HH4-2003-9; NEP-LTOP-HH5-2001-9; NEP-LTOP-HH5-2002-4; NEP-LTOP-HH5-2002-9; NEP-LTOP-HH5-2003-4; NEP-LTOP-HH5-2003-7; NEP-LTOP-HH5-2003-9; NEP-LTOP-HH7-2001-9; NEP-LTOP-HH7-2002-4; NEP-LTOP-HH7-2002-9; NEP-LTOP-HH7-2003-7; NEP-LTOP-HH7-2003-9; NEP-LTOP-HH9-2002-4; NEP-LTOP-HH9-2002-9; NEP-LTOP-HH9-2003-9; NEP-LTOP-NH03-2002-2; NEP-LTOP-NH05-2002-2; NEP-LTOP-NH10-2002-12; NEP-LTOP-NH10-2002-2; NEP-LTOP-NH10-2002-7; NEP-LTOP-NH10-2002-9; NEP-LTOP-NH10-2003-2; NEP-LTOP-NH10-2003-4; NEP-LTOP-NH10-2003-7; NEP-LTOP-NH10-2003-9; NEP-LTOP-NH1-2002-12; NEP-LTOP-NH1-2002-7; NEP-LTOP-NH1-2003-4; NEP-LTOP-NH1-2003-7; NEP-LTOP-NH1-2003-9; NEP-LTOP-NH15-2001-11; NEP-LTOP-NH15-2001-3; NEP-LTOP-NH15-2001-7; NEP-LTOP-NH15-2001-9; NEP-LTOP-NH15-2002-12; NEP-LTOP-NH15-2002-2; NEP-LTOP-NH15-2002-4; NEP-LTOP-NH15-2002-7; NEP-LTOP-NH15-2002-9; NEP-LTOP-NH15-2003-2; NEP-LTOP-NH15-2003-4; NEP-LTOP-NH15-2003-7; NEP-LTOP-NH15-2003-9; NEP-LTOP-NH20-2002-2; NEP-LTOP-NH20-2002-9; NEP-LTOP-NH20-2003-7; NEP-LTOP-NH25-2001-11; NEP-LTOP-NH25-2001-3; NEP-LTOP-NH25-2001-7; NEP-LTOP-NH25-2001-9; NEP-LTOP-NH25-2002-12; NEP-LTOP-NH25-2002-2; NEP-LTOP-NH25-2002-4; NEP-LTOP-NH25-2002-7; NEP-LTOP-NH25-2002-9; NEP-LTOP-NH25-2003-2; NEP-LTOP-NH25-2003-4; NEP-LTOP-NH25-2003-7; NEP-LTOP-NH25-2003-9; NEP-LTOP-NH3-2002-12; NEP-LTOP-NH3-2002-4; NEP-LTOP-NH3-2002-7; NEP-LTOP-NH3-2002-9; NEP-LTOP-NH3-2003-2; NEP-LTOP-NH3-2003-4; NEP-LTOP-NH3-2003-7; NEP-LTOP-NH3-2003-9; NEP-LTOP-NH35-2001-11; NEP-LTOP-NH35-2001-3; NEP-LTOP-NH35-2001-7; NEP-LTOP-NH35-2001-9; NEP-LTOP-NH35-2002-12; NEP-LTOP-NH35-2002-2; NEP-LTOP-NH35-2002-4; NEP-LTOP-NH35-2002-7; NEP-LTOP-NH35-2002-9; NEP-LTOP-NH35-2003-2; NEP-LTOP-NH35-2003-4; NEP-LTOP-NH35-2003-7; NEP-LTOP-NH35-2003-9; NEP-LTOP-NH45-2001-3; NEP-LTOP-NH45-2001-7; NEP-LTOP-NH45-2001-9; NEP-LTOP-NH45-2002-12; NEP-LTOP-NH45-2002-2; NEP-LTOP-NH45-2002-4; NEP-LTOP-NH45-2002-7; NEP-LTOP-NH45-2002-9; NEP-LTOP-NH45-2003-2; NEP-LTOP-NH45-2003-4; NEP-LTOP-NH45-2003-7; NEP-LTOP-NH45-2003-9; NEP-LTOP-NH5-2001-11; NEP-LTOP-NH5-2001-3; NEP-LTOP-NH5-2001-7; NEP-LTOP-NH5-2001-9; NEP-LTOP-NH5-2002-12; NEP-LTOP-NH5-2002-4; NEP-LTOP-NH5-2002-7; NEP-LTOP-NH5-2002-9; NEP-LTOP-NH5-2003-2; NEP-LTOP-NH5-2003-4; NEP-LTOP-NH5-2003-7; NEP-LTOP-NH5-2003-9; NEP-LTOP-NH55-2002-4; NEP-LTOP-NH55-2003-2; NEP-LTOP-NH55-2003-9; NEP-LTOP-NH65-2001-3; NEP-LTOP-NH65-2001-7; NEP-LTOP-NH65-2001-9; NEP-LTOP-NH65-2002-12; NEP-LTOP-NH65-2002-2; NEP-LTOP-NH65-2002-4; NEP-LTOP-NH65-2002-7; NEP-LTOP-NH65-2002-9; NEP-LTOP-NH65-2003-2; NEP-LTOP-NH65-2003-4; NEP-LTOP-NH65-2003-7; NEP-LTOP-NH65-2003-9; NEP-LTOP-NH85-2001-3; NEP-LTOP-NH85-2001-7; NEP-LTOP-NH85-2001-9; NEP-LTOP-NH85-2002-12; NEP-LTOP-NH85-2002-4; NEP-LTOP-NH85-2002-7; NEP-LTOP-NH85-2002-9; NEP-LTOP-NH85-2003-2; NEP-LTOP-NH85-2003-4; NEP-LTOP-NH85-2003-7; NEP-LTOP-NH85-2003-9; NEP-LTOP-RR1-2001-9; NEP-LTOP-RR1-2002-4; NEP-LTOP-RR1-2002-7; NEP-LTOP-RR1-2003-4; NEP-LTOP-RR2-2001-3; NEP-LTOP-RR2-2001-9; NEP-LTOP-RR2-2002-4; NEP-LTOP-RR2-2002-7; NEP-LTOP-RR2-2003-4; NEP-LTOP-RR3-2001-3; NEP-LTOP-RR3-2001-9; NEP-LTOP-RR3-2002-4; NEP-LTOP-RR3-2002-7; NEP-LTOP-RR3-2003-4; NEP-LTOP-RR4-2001-9; NEP-LTOP-RR4-2002-4; NEP-LTOP-RR4-2002-7; NEP-LTOP-RR4-2003-4; NEP-LTOP-RR6-2001-9; NEP-LTOP-RR6-2002-4; NEP-LTOP-RR6-2002-7; NEP-LTOP-RR6-2003-4; NEP-LTOP-RR7-2001-9; NEP-LTOP-RR7-2002-4; NEP-LTOP-RR7-2002-7; NEP-LTOP-RR7-2003-4; NIS; Northeast Pacific; Prokaryotes
    Type: Dataset
    Format: text/tab-separated-values, 1725 data points
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    DATA PANGAEA
  • 2
    Electronic Resource
    Electronic Resource
    Protozoa in Planktonic Food Webs, (1985)
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 32 (1985), S. 0 
    Details
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Protozoa are now being recognized as important members of planktonic food webs. This is due to the inclusion of microbial links in our paradigm of trophic relationships. Heterotrophic microflagellates and ciliates are major grazers of bacteria. They can stimulate production through nutrient recycling and can transform microbial production into larger particles, which are then available for macroconsumers. In this paper we add new groups, the small (〈 20 μm) ciliates and myxotrophic flagellates, to the planktonic food web.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1111/j.1550-7408.1985.tb04036.x
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    Paper (German National Licenses)
    Fulltext
  • 3
    Electronic Resource
    Electronic Resource
    High rates of consumption of bacteria by pelagic ciliates (1987)
    [s.l.] : Nature Publishing Group
    Nature 325 (1987), S. 710-711 
    Details
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Water samples containing natural assemblages of ciliates were collected in the Duplin River, a salt marsh tidal embayment on the Georgia, US coast. Ciliates were not taxonomically identified, except for one scuticociliate, Uronema marina, which we cultured on a wheat grain infusion. However, based ...
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1038/325710a0
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  • 4
    Electronic Resource
    Electronic Resource
    β-Glucosaminidase activity in marine microbes (1999)
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology ecology 28 (1999), S. 0 
    Details
    ISSN: 1574-6941
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Activity at acidic pH (4.5) of β-glucosaminidase (βGAM) has been suggested as a quantitative marker for biomass of bacterivorous protists in aquatic ecosystems. βGAM is an enzyme that cleaves peptidoglycan, a major component of bacterial cell walls. Measuring the rate of cleavage of the fluorochrome methylumbelliferone (MUF) from the fluorogenic substrate MUF-N-acetyl-β-d-glucosaminide (MUF-[GlcNAc]) is a simple assay for in situ activity of βGAM. However, this approach is seriously compromised by three characteristics of the enzyme: (1) all classes of marine microbes tested: bacteria, protists, and phytoplankton, exhibit βGAM activity, (2) the pH maximum for activity of βGAM is in the range of 6–8 for all classes of marine microbes, and (3) some species of marine phytoplankton have relatively high cell-specific and volume-specific βGAM activities at pH 4.5 and/or pH 7. Based on these results, enzymatic cleavage of the MUF-[GlcNAc] substrate does not appear to be useful as a specific assay for in situ biomass of heterotrophic protists, although the method could be applied in defined culture experiments.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1111/j.1574-6941.1999.tb00566.x
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  • 5
    Electronic Resource
    Electronic Resource
    Reply to the comment of J. Vrba: Problems with enzyme-based methods (2000)
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology ecology 33 (2000), S. 0 
    Details
    ISSN: 1574-6941
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1111/j.1574-6941.2000.tb00730.x
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  • 6
    Electronic Resource
    Electronic Resource
    Direct use of high molecular weight polysaccharide by heterotrophic flagellates (1988)
    [s.l.] : Nature Publishing Group
    Nature 335 (1988), S. 348-351 
    Details
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Samples containing natural assemblages of protozoa were collected from the surface waters of the salt marsh estuary adjacent to Sapelo Island, Georgia, and from a freshwater pond on the south end of the island. For dextran-uptake experiments, samples were prescreened through IS-jjum-mesh Nitex ...
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1038/335348a0
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  • 7
    Electronic Resource
    Electronic Resource
    And now, small is plentiful (1989)
    [s.l.] : Nature Publishing Group
    Nature 340 (1989), S. 429-429 
    Details
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] ON PAGE 467 of this issue1, Bergh et al. report the use of transmission electron microscopy to make direct counts of femtoplankton - viruses of less than 0.2 urn in size2 in natural waters. They find up to 108 viruses per ml, which is three to seven orders of magnitude higher than previous ...
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1038/340429a0
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  • 8
    Electronic Resource
    Electronic Resource
    New technologies needed (1991)
    [s.l.] : Nature Publishing Group
    Nature 352 (1991), S. 752-752 
    Details
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] SIR — I am appalled by your article "Many catastrophes too many" (Nature 351, 171-172; 1991), and its reaffirma-tion of simplistic and fatally incorrect mainstream ideas on the economic de-velopment of poor nations. Modern eco-nomic theory, which is founded on the notion of continual growth, ...
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1038/352752a0
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  • 9
    Electronic Resource
    Electronic Resource
    Trophic interactions within pelagic microbial communities: Indications of feedback regulation of carbon flow (1988)
    Springer
    Hydrobiologia 159 (1988), S. 19-26 
    Details
    ISSN: 1573-5117
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Future considerations of carbon-energy flows within pelagic food webs should include internal, biotic feedback controls, in addition to abiotic forcing functions, in the regulation of these flows. Over the past two decades, research on microbial communities of pelagic ecosystems has yielded data suggestive of cybernetic-like regulation operating within these communities. As presently conceived, phagotrophic protozoa have a pivotal role in such regulation as a consequence of their rapid growth, grazing, and nutrient regenerative capabilities. Feedback controls within microbial food webs may have significant effects on distal portions of pelagic ecosystems, including the fate of organic detritus and metazoan production.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00007364
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  • 10
    facet.materialart.
    Unknown
    Trophic interactions within pelagic microbial communities: Indications of feedback regulation of carbon flow (1988)
    Springer
    Details
    Publication Date: 1988-03-01
    Print ISSN: 0018-8158
    Electronic ISSN: 1573-5117
    Topics: Biology
    Published by Springer
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    PAPER CURRENT
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