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  • 1
    Online Resource
    Online Resource
    Newark :John Wiley & Sons, Incorporated,
    Keywords: Tintinnida. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (322 pages)
    Edition: 2nd ed.
    ISBN: 9781118358115
    DDC: 579.4/9
    Language: English
    Note: Intro -- Title page -- Copyright page -- Contents -- Contributors -- Chapter 1: Introduction to Tintinnids -- 1.1 Why A Book on Tintinnid Ciliates? -- 1.2 What Is A Tintinnid Ciliate? -- 1.3 The Lorica As the Defining Characteristic of Tintinnid Ciliates -- 1.4 History of Tintinnid Studies -- 1.5 Tintinnids As Model Organisms for Marine Plankton -- 1.6 Key Points -- Acknowledgments -- Chapter 2: The Tintinnid Lorica -- 2.1 Introduction -- 2.2 Diversity, Formation, and Variability of Loricae -- Diversity of loricae -- General aspects of lorica formation -- Lorica material -- Role of the somatic cilia -- Lorica phenotypes formed during the cell cycle -- Variability of loricae during the cell cycle in hyaline species -- Formation of hard, agglomerated loricae -- Soft, agglomerated loricae -- Problems of lorica typological taxa -- 2.3 Ultrastructure of Loricae -- 2.4 Chemical Composition of Loricae -- History of chemical studies -- Cytochemical stains and enzymatic experiments -- 2.5 Lorica Sedimentation -- 2.6 Key Points -- Acknowledgments -- Chapter 3: Systematics and Evolution of Tintinnid Ciliates -- 3.1 Introduction -- 3.2 History of Tintinnid Taxonomy and Systematics -- The beginning -- The introduction of staining techniques -- The era of electron microscopy -- Cladistic analysis -- Gene sequence analysis -- Species descriptions and redescriptions -- Monographs and identification keys -- 3.3 Evolution of Tintinnids -- Kinetal maps -- The ancestor of the stichotrichs, halteriids, oligotrichids, and choreotrichids -- The ancestor of the halteriids, oligotrichids, and choreotrichids -- The ancestor of the oligotrichids and choreotrichids -- The ancestor of the choreotrichids -- The early evolution within the tintinnids -- Freshwater species -- Marine species -- The capsule types -- The lorica sac -- Cladistic analysis -- Conclusions. , 3.4 How to Read the Tintinnid Cladogram -- 3.5 Molecular Analysis and Comparison with Morphologic Data -- Gene sequence analysis in general -- Data acquisition -- SSU rRNA phylogenies -- Comparison of SSU rRNA phylogenies and cladograms with former hypothesis -- 3.6 Systematics -- Recent changes in the classification -- Additional changes -- 3.7 Comparison with the Evolution of Related Planktonic Ciliates: The Aloricate Choreotrichids, Oligotrichids, and Halteriids -- The planktonic life style -- The somatic ciliature -- Resting cysts -- The halteriids, an enigmatic ciliate group -- Gene sequence analyses -- 3.8 Key Points -- Acknowledgments -- Chapter 4: Ecophysiology and Behavior of Tintinnids -- 4.1 Introduction -- 4.2 Feeding -- An overview of tintinnid feeding -- Functional response -- Size selectivity -- Selectivity other than size -- 4.3 Growth -- An overview of tintinnid growth -- Population growth -- Numerical response -- Scaling tintinnid maximum growth rate to size -- Cell size, number, and growth rate -- Gross growth and assimilation efficiency -- 4.4 Swimming Behavior -- The basics of swimming -- An assessment of swimming motion -- Changes in swimming behavior -- Swimming synthesis -- 4.5 Response to Abiotic Factors and Interactions with Biotic Factors -- Temperature -- Other abiotic factors -- 4.6 Tintinnids as Models and in Models -- General models -- Favella -- Incorporation of tintinnids into models -- 4.7 Key Points -- Acknowledgments -- Chapter 5: Predators of Tintinnids -- 5.1 Introduction -- 5.2 Predators of Tintinnids -- Other protists -- Copepods -- Euphausiids and other large crustacean zooplankton -- Gelatinous zooplankton including cnidarians, ctenophores, chaetognaths, pteropods and pelagic tunicates -- Other holoplankton -- Ichthyoplankton -- Larvae and adults of benthic invertebrates. , 5.3 Anti-Predator Defenses of Tintinnids -- 5.4 Top-down Control of Tintinnids -- 5.5 Importance of Tintinnids as Prey for the Predator -- 5.6 Tintinnids as Vectors for Algal Toxins -- 5.7 Key Points -- Acknowledgments -- Chapter 6: Parasites of Tintinnids -- 6.1 Background -- Heterotrophic symbionts of ciliates -- Discovery of tintinnid parasites -- 6.2 Dinoflagellate Parasites: Morphology and Infection Cycle -- Syndinean parasites -- Dinophycean parasites -- Sexuality -- Key to the dinoflagellate parasites of tintinnids -- 6.3 Molecular Evolution of Dinoflagellates Parasitizing Tintinnids -- Placement of tintinnid parasites within the dinoflagellates -- Dinokaryote parasites of tintinnids -- Syndinean parasites of tintinnids -- 6.4 Ecology of Tintinnid Parasites -- Distribution, seasonality, and host range -- Parasite prevalence and impact on host populations -- 6.5 Summary and Future Directions -- 6.6 Key Points -- Acknowledgments -- Chapter 7: Comparative Biology of Tintinnid Cysts -- 7.1 Introduction -- What is a cyst? -- Historical overview of tintinnid and aloricate ciliate cysts -- 7.2 Morphology -- Characteristics of tintinnid cysts observed in seawater samples -- Characteristics of oligotrich and dinoflagellate cysts -- 7.3 Encystment and Excystment -- Encystment -- Factors inducing encystment -- Factors inducing excystment -- 7.4 Ecological Function of Cysts -- Distribution of tintinnid cysts in coastal sediments -- Influence of excystment and encystment on population dynamics -- 7.5 Key Points -- Acknowledgments -- Chapter 8: Fossil Tintinnids -- 8.1 Introduction: A Paucity of Data -- 8.2 Proterozoic Tintinnids: No Evidence of a Beginning -- 8.3 Paleozoic Tintinnid Reports: Too Thin to Know -- 8.4 Mesozoic Tintinnids and Calpionellids: Same Shape, Different Composition -- 8.5 Cenozoic Tintinnids: Sparse. , 8.6 Organic and Agglutinated Phanerozoic Fossils: The Most Likely Candidates -- 8.7 Conclusions and Perspectives -- 8.8 Key Points -- Acknowledgments -- Chapter 9: Tintinnids in Microzooplankton Communities -- 9.1 Ecology of Microzooplankton -- Microzooplankton as a functional trophic category -- Composition of microzooplankton assemblages -- Grazing impact of microzooplankton -- Nutrient regeneration by microzooplankton -- Microzooplankton as food for higher trophic levels -- 9.2 Quantitative Importance of Tintinnids in Microzooplankton Assemblages -- Abundance and biomass -- Grazing -- Tintinnids as prey for other zooplankton -- In situ growth -- 9.3 Characteristics That Set Tintinnids Apart from Other Microzooplankton -- The lorica -- Obligate planktonic habitat -- Strict heterotrophy? -- 9.4 Key Points -- Acknowledgments -- Chapter 10: Diversity and Distributions of Tintinnids -- 10.1 Introduction -- 10.2 Biogeography -- Global biogeography -- Distribution-abundance relationships -- Latitudinal diversity gradient -- 10.3 Assemblages of Coastal Systems -- Seasonal changes in species richness -- Seasonal changes in morphotypes -- 10.4 Assemblages of Open Waters -- 10.5 Key Points -- Acknowledgments -- References -- Organism Index -- Subject Index -- Supplemental Images.
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 35 (1988), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Inc
    The @journal of eukaryotic microbiology 52 (2005), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Microzooplankton grazing can be important in regulating growth of dinoflagellate populations, including species responsible for harmful algal blooms. In the Chesapeake Bay region, microzooplankton community grazing coefficients on small cell-size dinoflagellates are often greater than potential gross growth coefficients of dinoflagellates, and thus grazing may prevent bloom formation. Who are the major microzooplankton grazers on small dinoflagellates? Ciliates or other dinoflagellates? Data from Chesapeake Bay and its tributaries indicate both; sometimes ciliates and sometimes dinoflagellates are the major grazers. The importance of ciliates and heterotrophic dinoflagellates varies with season and location, but often one group dominates the microzooplankton assemblage. Specific clearance and division rates of ciliates are higher than that of heterotrophic dinoflagellates, thus it could be expected that ciliates would be the dominant microzooplankton grazers. However, during summer, small heterotrophic dinoflagellates are often the dominant grazers on small dinoflagelllates in the mesohaline Bay. Differential predation by copepods on ciliates may be responsible for this pattern. When microzooplankton community grazing is less than dinoflagellate cell division, red tides may result. Thus, it is important to understand the factors controlling both ciliate and heterotrophic dinoflagellate populations and their grazing impacts.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science Inc
    The @journal of eukaryotic microbiology 52 (2005), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Myrionecta rubra and Mesodinium pulex are among the most commonly encountered planktonic ciliates in coastal marine and estuarine regions throughout the world. Despite their widespread distribution, both ciliates have received little attention by taxonomists. In order to understand the phylogenetic position of these ciliates better, we determined the SSU rRNA gene from cultures of M. rubra and M. pulex. Partial sequence data were also generated from isolated cells of M. rubra from Chesapeake Bay. The M. rubra and M. pulex sequences were very divergent from all other ciliates, but shared a branch with 100% bootstrap support. Both species had numerous deletions and substitutions in their SSU rRNA gene, resulting in a long branch for the clade. This made the sequences prone to spurious phylogenetic affiliations when using simple phylogenetic methods. Maximum likelihood analysis placed M. rubra and M. pulex on the basal ciliate branch, following the removal of ambiguously aligned regions. Fluorescent in situ hybridization probes were used with confocal laser scanning microscopy to confirm that these divergent sequences were both expressed in the cytoplasm and nucleolus of M. rubra and M. pulex. We found that our sequence data matched several recently discovered unidentified eukaryotes in Genbank from diverse marine habitats, all of which had apparently been misattributed to highly divergent amoeboid organisms.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of eukaryotic microbiology 46 (1999), S. 0 
    ISSN: 1550-7408
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Mixotrophy, used herein for the combination of phototrophy and phagotrophy, is widespread among dinoflagellates. It occurs among most, perhaps all, of the extant orders, including the Prorocentrales, Dinophysiales. Gymnodiniales, Noctilucales, Gonyaulacales, Peridiniales, Blastodiniales. Phytodiniales, and Dinamoebales. Many cases of mixotrophy among dinoflagellates are probably undocumented. Primarily photosynthetic dinoflagellates with their “own” plastids can often supplement their nutrition by preying on other cells. Some primarily phagotrophic species are photosynthetic due to the presence of kleptochloroplasts or algal endosymbionts. Some parasitic dinoflagellates have plastids and are probably mixotrophic. For most mixotrophic dinoflagellates, the relative importance of photosynthesis, uptake of dissolved inorganic nutrients, and feeding are unknown. However, it is apparent that mixotrophy has different functions in different physiological types of dinoflagellates. Data on the simultaneous regulation of photosynthesis, assimilation of dissolved inorganic and organic nutrients, and phagotophy by environmental parameters (irradiance. availablity of dissolved nutrients, availability of prey) and by life history events are needed in order to understand the diverse roles of mixotrophy in dinoflagellates.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] It is well documented that organelles can be retained and used by predatory organisms, but in most cases such sequestrations are limited to plastids of algal prey. Furthermore, sequestrations of prey organelles are typically highly ephemeral as a result of the inability of the organelle to ...
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Mesodinium rubrum (Lohmann 1908) Jankowski 1976 (= Myrionecta rubra) is a common photosynthetic marine planktonic ciliate which can form coastal red-tides. It may represent a ‘species complex’ and since Darwin's voyage on the Beagle, it has been of great cytological, ...
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 503 (1987), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 326 (1987), S. 790-792 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Surface water samples were collected from the Oceanographic Institution dock in Great Harbor, Woods Hole, Massachusetts and the planktonic ciliates were enumerated (Fig. 1). This location is well mixed by tidal currents, and thus stratification of the water column is minimal, and samples could be ...
    Type of Medium: Electronic Resource
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  • 10
    Publication Date: 2024-02-01
    Keywords: 5191045; AT_II-119/5_26-4; Atlantis_II-119/5; Atlantis II (1963); Bacteria, heterotrophic; Bottle number; Ciliates, non-oligotrich, other; Ciliates, non-oligotrich, other, biomass as carbon; Ciliates, non-plastidic-oligotrich; Ciliates, non-plastidic-oligotrich, biomass as carbon; Ciliates, oligotrich, other; Ciliates, oligotrich, other, biomass as carbon; Ciliates, plastidic-oligotrich; Ciliates, plastidic-oligotrich, biomass as carbon; Copepoda, nauplii; Copepoda, other; CTD/Rosette; CTD-RO; Cyanobacteria; Cyanobacteria, biomass as carbon; Cyanobacteria, biovolume; Cyanobacteria, cell biovolume; DEPTH, water; Dinoflagellates, heterotrophic; Dinoflagellates, heterotrophic, biomass as carbon; Dinoflagellates, heterotrophic, standard deviation; Foraminifera; JGOFS; Joint Global Ocean Flux Study; Leucine incorporation rate; Mesodinium; Mesodinium, biomass as carbon; NABE; Nanoplankton, heterotrophic; Nanoplankton, heterotrophic, biomass as carbon; Nanoplankton, heterotrophic, biovolume; Nanoplankton, phototrophic; Nanoplankton, phototrophic, biomass as carbon; Nanoplankton, phototrophic, biovolume; North Atlantic; North Atlantic Bloom Experiment, 1989-1991; Plankton, heterotrophic, cell biovolume; Plankton, phototrophic, cell biovolume; Pressure, water; Sticholonche; Tintinnid; Tintinnid, biomass as carbon
    Type: Dataset
    Format: text/tab-separated-values, 409 data points
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