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A study of reproduction and other life cycle phenomena in planktonic protists using an acridine orange fluorescence technique

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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The development of the macronucleus in the ciliated protozoan Stylonychia mytilus
inferredcites →https://doi.org/10.1007/bf00285634openalex-snapshot
Morphology and development of the macronuclei of the ciliates Stylonychia mytilus and Euplotes aediculatus
inferredcites →https://doi.org/10.1007/bf00352450openalex-snapshot
Microgamete formation and the growth rate of Tintinnopsis beroidea
inferredcites →https://doi.org/10.1007/bf00386854openalex-snapshot
Studies on the functional role of tintinnids in the Southern California Bight. III. Grazing impact of natural assemblages
inferredcites →https://doi.org/10.1007/bf00390938openalex-snapshot
A spatial model of phytoplankton patchiness
inferredcites →https://doi.org/10.1007/bf00395638openalex-snapshot
Studies on the functional role of tintinnids in the Southern California Bight. I. Grazing and growth rates in laboratory cultures
inferredcites →https://doi.org/10.1016/0011-7471(72)90030-7openalex-snapshot
The phased division and cytological characteristics of Pyrocystis spp. can be used to estimate doubling times of their populations in the sea
inferredcites →https://doi.org/10.1016/0011-7471(75)90055-8openalex-snapshot
Phased cell division in natural populations of the marine diatom Ditylum brightwelli and the potential significance of diel phytoplankton behavior in the sea
inferredcites →https://doi.org/10.1016/0022-0981(76)90126-xopenalex-snapshot
Phased cell division in natural populations of marine dinoflagellates from shipboard cultures
inferredcites →https://doi.org/10.1016/0022-0981(79)90002-9openalex-snapshot
Temporal pattern of division in the dinoflagellate genus ceratium and its application to the determination of growth rate
inferredcites →https://doi.org/10.1016/0022-0981(80)90052-0openalex-snapshot
Phased cell division in natural and laboratory populations of marine planktonic diatoms
inferredcites →https://doi.org/10.1016/0022-1694(72)90028-5openalex-snapshot
A manual on methods for the assessment of secondary productivity in fresh waters
inferredcites →https://doi.org/10.1016/0026-265x(79)90052-3openalex-snapshot
Principles and techniques of electron microscopy, vol. 7. Biological applications
inferredcites →https://doi.org/10.1016/b978-0-08-016437-3.50005-5openalex-snapshot
NUCLEAR PHENOMENA DURING CONJUGATION AND AUTOGAMY IN CILIATES
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CELL DIVISION PERIODICITY IN 13 SPECIES OF MARINE PHYTOPLANKTON ON A LIGHT: DARK CYCLE1
inferredcites →https://doi.org/10.1111/j.1529-8817.1979.tb02964.xopenalex-snapshot
CELL DIVISION PERIODICITY IN 13 SPECIES OF MARINE PHYTOPLANKTON ON A LIGHT: DARK CYCLE1
inferredcites →https://doi.org/10.1111/j.1550-7408.1969.tb02308.xopenalex-snapshot
Tintinnida: Feeding Experiments and Lorica Development1
inferredcites →https://doi.org/10.1111/j.1550-7408.1977.tb00982.xopenalex-snapshot
Timing and Regulation of Nuclear and Cortical Events in the Cell Cycle of Tetrahymena pyriformis*
inferredcites →https://doi.org/10.1139/f70-168openalex-snapshot
Spatial Heterogeneity of Phytoplankton in a Near-Shore Environment
inferredcites →https://doi.org/10.2307/1540679openalex-snapshot
STUDIES ON THE SIZES, SHAPES, AND THE DEVELOPMENT OF THE LORICA OF AGGLUTINATED TINTINNIDA
inferredcites →https://doi.org/10.2307/1933452openalex-snapshot
Reproductive Rate of Copepods in Nature and Its Relation to Phytoplankton Population
inferredcites →https://doi.org/10.2307/1937111openalex-snapshot
An Experimental Approach to the Dynamics of a Natural Population of Daphnia Galeata Mendotae
inferredcites →https://doi.org/10.2307/3224301openalex-snapshot
Essentials of Practical Microtechnique
inferredcites →https://doi.org/10.2307/3225420openalex-snapshot
Essentials of Practical Microtechnique
inferredcites →https://doi.org/10.2307/3225561openalex-snapshot
Principles and Techniques of Electron Microscopy
inferredcites →https://doi.org/10.4319/lo.1974.19.6.0902openalex-snapshot
The use of a deep tank in plankton ecology. 2. Efficiency of a planktonic food chain1
inferredcites →https://doi.org/10.4319/lo.1976.21.6.0784openalex-snapshot
Some consequences of distributional heterogeneity of phytoplankton and zooplankton1
inferredcites →https://doi.org/10.4319/lo.1978.23.3.0518openalex-snapshot
Silicic acid incorporation in marine diatoms on light:dark cycles: Use as an assay for phased cell division 1
inferredcites →https://doi.org/10.4319/lo.1980.25.3.0430openalex-snapshot
The egg production of a marine planktonic copepod in relation to its food supply: Laboratory studies1
inferredcites →https://doi.org/10.4319/lo.1980.25.4.0610openalex-snapshot
Population structure and in situ division rates of Ceratium in oligotrophic waters of the North Pacific central gyre1

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Fauna of tintinnids (Tintinnida, Ciliata) during an Arctic-Antarctic cruise, with the S/V “Croatian Tern”
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Variations in biochemical parameters of Heterocapsa sp. and Olisthodiscus luteus grown in 12:12 light:dark cycles
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Variations in biochemical parameters of Heterocapsa sp. and Olisthodiscus luteus grown in 12:12 light:dark cycles I. Cell cycle and nucleic acid composition
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Grazing of the mixotrophic dinoflagellate Gymnodinium sanguineum on ciliate populations of Chesapeake Bay
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Dinoflagellate infections of Favella panamensis from two North American estuaries
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Growth of Favella sp. (Ciliata: Tintinnina) and other microzooplankters in cages incubated in situ and comparison to growth in vitro
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Spatial and temporal occurrence of the parasitic dinoflagellate Duboscquella cachoni and its tintinnine host Eutintinnus pectinis in Chesapeake Bay
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Microphagous ciliates in mesohaline Chesapeake Bay waters: Estimates of growth rates and consumption by copepods
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Dinopallor Comventus n. gen., n. sp., a Novel Parasitoid of Marine Dinoflagellates Representing a Sister Lineage to Seagrass Parasites and Expanding the Host Range of Phytomyxea (Rhizaria, Endomyxa)
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Cultivation of shear stress sensitive and tolerant microalgal species in a tubular photobioreactor equipped with a centrifugal pump
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Trophic biology of phaeodarian radiolarians and flux of living radiolarians in the upper 2000 m of the North Pacific central gyre
inferred← citeshttps://doi.org/10.1016/0272-7714(89)90069-3openalex-snapshot
Estimates of in situ population growth rates of four tintinnine ciliate species near Kingston Harbour, Jamaica
inferred← citeshttps://doi.org/10.1016/0272-7714(90)90044-ropenalex-snapshot
Seasonal abundances of planktonic ciliates and microflagellates in mesohaline Chesapeake Bay waters
inferred← citeshttps://doi.org/10.1016/0272-7714(91)90003-topenalex-snapshot
Guilds of ciliate microzooplankton in the Chesapeake Bay
inferred← citeshttps://doi.org/10.1016/j.ecss.2005.01.013openalex-snapshot
Temporal variability of optical properties in a shallow, eutrophic estuary: Seasonal and interannual variability
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Phylogeny of the order Choreotrichida (Ciliophora, Spirotricha, Oligotrichea) as inferred from morphology, ultrastructure, ontogenesis, and SSrRNA gene sequences
inferred← citeshttps://doi.org/10.1016/j.ejop.2012.08.003openalex-snapshot
A modified dilution method reveals higher protozoan growth rates than the size fractionation method
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The interplay between host toxins and parasitism by Amoebophrya
inferred← citeshttps://doi.org/10.1016/j.protis.2011.11.007openalex-snapshot
Ultrastructure of Amoebophrya sp. and its Changes during the Course of Infection
inferred← citeshttps://doi.org/10.1016/j.protis.2015.08.005openalex-snapshot
Do All Dinoflagellates have an Extranuclear Spindle?
inferred← citeshttps://doi.org/10.1016/s0167-7012(03)00042-3openalex-snapshot
The edaphic quantitative protargol stain: a sampling protocol for assessing soil ciliate abundance and diversity
inferred← citeshttps://doi.org/10.1016/s0932-4739(11)80303-2openalex-snapshot
Morphogenesis in some freshwater Tintinnids (Ciliophora, Oligotrichida)
inferred← citeshttps://doi.org/10.1017/s0025315400090093openalex-snapshot
Ciliate growth rates from Plymouth Sound: comparison of direct and indirect estimates
inferred← citeshttps://doi.org/10.1038/s41467-022-28867-8openalex-snapshot
Mucospheres produced by a mixotrophic protist impact ocean carbon cycling
inferred← citeshttps://doi.org/10.1038/s41598-022-26004-5openalex-snapshot
Protistan epibionts affect prey selectivity patterns and vulnerability to predation in a cyclopoid copepod
inferred← citeshttps://doi.org/10.1046/j.1529-8817.2002.01200.xopenalex-snapshot
PARASITISM OF PHOTOSYNTHETIC DINOFLAGELLATES BY THREE STRAINS OF AMOEBOPHRYA (DINOPHYTA): PARASITE SURVIVAL, INFECTIVITY, GENERATION TIME, AND HOST SPECIFICITY1
inferred← citeshttps://doi.org/10.1080/11263508909430254openalex-snapshot
Reproduction and cyst formation in Scrippsiella precaria (Dinophyceae)
inferred← citeshttps://doi.org/10.1098/rsif.2021.0860openalex-snapshot
Reproduction dynamics of planktonic microbial eukaryotes in the open ocean
inferred← citeshttps://doi.org/10.1111/j.0022-3646.1984.00351.xopenalex-snapshot
SEXUAL PROCESSES IN THE LIFE CYCLE OFGYRODINIUM UNCATENUM(DINOPHYCEAE): A MORPHOGENETIC OVERVIEW1
inferred← citeshttps://doi.org/10.1111/j.0022-3646.1992.00267.xopenalex-snapshot
EFFECTS OF TURBULENCE ON THE MARINE DINOFLAGELLATE GYMNODINIUM NELSONII1
inferred← citeshttps://doi.org/10.1111/j.1529-8817.1986.tb00013.xopenalex-snapshot
CELL DIVISION RATES OF EUCARYOTIC ALGAE MEASURED BY TRITIATED THYMIDINE INCORPORATION INTO DNA: COINCIDENT MEASUREMENTS OF PHOTOSYNTHESIS AND CELL DIVISION OF INDIVIDUAL SPECIES OF PHYTOPLANKTON ISOLATED FROM NATURAL POPULATIONS
inferred← citeshttps://doi.org/10.1111/j.1529-8817.1986.tb00043.xopenalex-snapshot
OCCURRENCE OF RICHELIA INTACELLULARIS (CYANOPHYTA)WITHIN THE DIATOMMMS HEMIAULUS HAUKII ADN H. MEMBRANACEUS OFF HAWAII1
inferred← citeshttps://doi.org/10.1111/j.1529-8817.1987.tb04215.xopenalex-snapshot
ULTRASTRUCTURE OF A NEW INTRACELLULAR SYMBIOTIC ALGA FOUND WITHIN PLANKTONIC FORAMINIFERA1
inferred← citeshttps://doi.org/10.1111/j.1529-8817.2004.04002.xopenalex-snapshot
INFECTION OF THE BLOOM‐FORMING THECATE DINOFLAGELLATES ALEXANDRIUM AFFINE AND GONYAULAX SPINIFERA BY TWO STRAINS OF AMOEBOPHRYA (DINOPHYTA)1
inferred← citeshttps://doi.org/10.1111/j.1529-8817.2007.00392.xopenalex-snapshot
Species‐specific physiological response of dinoflagellates to quantified small‐scale turbulence1
inferred← citeshttps://doi.org/10.1111/j.1529-8817.2009.00649.xopenalex-snapshot
DINOFLAGELLATE HOST‐PARASITE STEROL PROFILES DICTATE KARLOTOXIN SENSITIVITY1
inferred← citeshttps://doi.org/10.1111/j.1550-7408.1988.tb04159.xopenalex-snapshot
Duboscquella cachoni N. Sp., a Parasitic Dinoflagellate Lethal to Its Tintinnine Host Eutintinnus pectinis1
inferred← citeshttps://doi.org/10.1111/j.1550-7408.1992.tb01286.xopenalex-snapshot
Morphology and Infraciliature of Three Species of Eutintinnus (Ciliophora; Tintinnina) with Guidelines for Interpreting Protargol‐Stained Tintinnine Ciliates
inferred← citeshttps://doi.org/10.1111/j.1550-7408.1993.tb04881.xopenalex-snapshot
Spatial and Temporal Aspects of Mixotrophy In Chesapeake Bay Dinoflagellates
inferred← citeshttps://doi.org/10.1111/j.1550-7408.1994.tb01520.xopenalex-snapshot
Occurrence of the Parasitic Dinoflagellate Amoebophrya ceratii in Chesapeake Bay Populations of Gymnodinium sanguineum
inferred← citeshttps://doi.org/10.1111/j.1550-7408.1995.tb01577.xopenalex-snapshot
Kyaroikeus cetarius N. G., N. Sp.: A Parasitic Ciliate from the Respiratory Tract of Odonticete Cetacea
inferred← citeshttps://doi.org/10.1111/j.1550-7408.1996.tb04490.xopenalex-snapshot
Stomatogenesis in Kyaroikeus cetarius (Dysteriina, Kyaroikeidae, N. Fam.): Clues to Its Systematic Placement
inferred← citeshttps://doi.org/10.1111/j.1550-7408.1998.tb04527.xopenalex-snapshot
Stomatogenesis of the Ciliate Genus Strombidinopsis with an Improved Description of S. spiniferum and S. acuminatum
inferred← citeshttps://doi.org/10.1111/j.1550-7408.1999.tb06060.xopenalex-snapshot
The Feeding Ecology of Actinophrys sol (Sarcodina: Heliozoa) in Chesapeake Bay
inferred← citeshttps://doi.org/10.1111/j.1550-7408.2000.tb00082.xopenalex-snapshot
Infection of Gymnodinium sanguineum by the Dinoflagellate Amoebophryasp.: Effect of Nutrient Environment on Parasite Generation Time, Reproduction, and Infectivity
inferred← citeshttps://doi.org/10.1111/j.1550-7408.2002.tb00343.xopenalex-snapshot
Ecology of the Red‐Tide Dinoflagellate Ceratium furca: Distribution, Mixotrophy, and Grazing Impact on Ciliate Populations of Chesapeake Bay
inferred← citeshttps://doi.org/10.1111/j.1550-7408.2004.tb00392.xopenalex-snapshot
Molecular Phylogeny of Phyllopharyngean Ciliates and their Group I Introns
inferred← citeshttps://doi.org/10.1111/j.1550-7408.2008.00326.xopenalex-snapshot
Morphological Characterization and Intraspecific Variation of Zoothamnium intermedium Precht, 1935 (Ciliophora, Peritrichia) Attached to Calanoid Copepods in the Chesapeake Bay, USA
inferred← citeshttps://doi.org/10.1111/j.1550-7408.2008.00378.xopenalex-snapshot
Sexual and Asexual Processes in Protoperidinium steidingerae Balech (Dinophyceae), with Observations on Life‐History Stages of Protoperidinium depressum (Bailey) Balech (Dinophyceae)
inferred← citeshttps://doi.org/10.1111/j.1550-7408.2009.00433.xopenalex-snapshot
Expressed Sequence Tags from Amoebophrya sp. Infecting Karlodinium veneficum: Comparing Host and Parasite Sequences
inferred← citeshttps://doi.org/10.1111/j.1550-7408.2010.00504.xopenalex-snapshot
Tintinnophagus acutus n. g., n. sp. (Phylum Dinoflagellata), an Ectoparasite of the Ciliate Tintinnopsis cylindrica Daday 1887, and Its Relationship to Duboscquodinium collini Grassé 1952
inferred← citeshttps://doi.org/10.1111/j.1550-7408.2011.00588.xopenalex-snapshot
Revision of the Family D uboscquellidae with Description of E uduboscquella crenulata n. gen., n. sp. ( D inoflagellata, S yndinea), an Intracellular Parasite of the Ciliate F avella panamensis Kofoid & Campbell,
inferred← citeshttps://doi.org/10.1111/j.1744-7410.2000.tb00169.xopenalex-snapshot
Planeticovorticella finleyi n.g., n.sp. (Peritrichia, Vorticellidae), a planktonic ciliate with a polymorphic life cycle
inferred← citeshttps://doi.org/10.1111/jeu.12252openalex-snapshot
Epistylis portoalegrensis n. sp. (Ciliophora, Peritrichia): A New Freshwater Ciliate Species from Southern Brazil
inferred← citeshttps://doi.org/10.1111/jeu.12496openalex-snapshot
Redescription of Tintinnopsis everta Kofoid and Campbell 1929 (Alveolata, Ciliophora, Tintinnina) Based on Taxonomic and Genetic Analyses—Discovery of a New Complex Ciliary Pattern
inferred← citeshttps://doi.org/10.1111/jeu.12728openalex-snapshot
Redescription of Antetintinnidium mucicola (Claparède and Lachmann, 1858) nov. gen., nov. comb. (Alveolata, Ciliophora, Tintinnina)
inferred← citeshttps://doi.org/10.1111/jeu.12879openalex-snapshot
Ecology of planktonic ciliates in a changing world: Concepts, methods, and challenges
inferred← citeshttps://doi.org/10.1128/aem.46.6.1388-1393.1983openalex-snapshot
Double-Staining Epifluorescence Technique to Assess Frequency of Dividing Cells and Bacteriovory in Natural Populations of Heterotrophic Microprotozoa
inferred← citeshttps://doi.org/10.1128/aem.51.4.769-775.1986openalex-snapshot
Radioisotopic Method for Measuring Cell Division Rates of Individual Species of Diatoms from Natural Populations
inferred← citeshttps://doi.org/10.1139/z87-092openalex-snapshot
Distribution and abundance of tintinnids in the Quoddy Region of the Bay of Fundy
inferred← citeshttps://doi.org/10.11646/zootaxa.3869.5.5openalex-snapshot
Description of Epistylis riograndensis n.sp. (Ciliophora: Peritrichia) found in an artificial lake in Southern Brazil
inferred← citeshttps://doi.org/10.11646/zootaxa.4508.2.4openalex-snapshot
Description of Two New Species of the Genus Vorticella (Ciliophora: Peritrichia) Epibionts on Pomacea canaliculata (Mollusca: Ampullariidae: Gastropoda) in Southern Brazil
inferred← citeshttps://doi.org/10.1186/s12866-025-03780-4openalex-snapshot
Morphologic changes in the model tintinnid Schmidingerella (Alveolata, Ciliophora) during the cell cycle, including the first volumetric analyses of the lorica-forming material
inferred← citeshttps://doi.org/10.1575/1912/1644openalex-snapshot
The ecology, life history, and phylogeny of the marine thecate heterotrophic dinoflagellates Protoperidinium and Diplopsalidaceae (Dinophyceae)
inferred← citeshttps://doi.org/10.1590/s1519-69842008000400013openalex-snapshot
Attachment of the peritrich epibiont Zoothamnium intermedium Precht, 1935 (Ciliophora, Peritrichia) to artificial substrates in a natural environment
inferred← citeshttps://doi.org/10.18174/336941openalex-snapshot
Microalgae for aquaculture
inferred← citeshttps://doi.org/10.2307/1466987openalex-snapshot
Guilds of Anuran Larvae: Relationships among Developmental Modes, Morphologies, and Habitats
inferred← citeshttps://doi.org/10.3354/ame01599openalex-snapshot
Influence of inorganic nutrients, irradiance, and time of day on food uptake by the mixotrophic dinoflagellate Neoceratium furca
inferred← citeshttps://doi.org/10.3354/ame01687openalex-snapshot
Observations on dinoflagellate parasites of aloricate ciliates in Korean coastal waters
inferred← citeshttps://doi.org/10.3354/ame028069openalex-snapshot
Ciliate grazing on the parasite Amoebophrya sp. decreases infection of the red-tide dinoflagellate Akashiwo sanguinea
inferred← citeshttps://doi.org/10.3354/ame029011openalex-snapshot
Effects of parasitism on diel vertical migration, phototaxis/geotaxis, and swimming speed of the bloom-forming dinoflagellate Akashiwo sanguinea
inferred← citeshttps://doi.org/10.3354/meps015225openalex-snapshot
Periodicities of photosynthesis and cell division: behavior of phase-lagged replicate cultures of Ditylum brightwellii in a diurnally varying photic regime
inferred← citeshttps://doi.org/10.3354/meps029117openalex-snapshot
Growth rates of natural tintinnid populations in Narragansett Bay
inferred← citeshttps://doi.org/10.3354/meps044287openalex-snapshot
Species-specific phytoplankton growth rates via diel DNA synthesis cycles. II DNA quantification and model verification in the dino-flagellate Heterocapsa triquetra
inferred← citeshttps://doi.org/10.3354/meps047239openalex-snapshot
Reproductive rates and periodicities of oceanic tintinnine ciliates
inferred← citeshttps://doi.org/10.3354/meps060075openalex-snapshot
Phagotrophy and fecal pellet production by an athecate dinoflagellate in Antarctic sea ice
inferred← citeshttps://doi.org/10.3354/meps227281openalex-snapshot
Effects of two strains of the parasitic dinoflagellate Amoebophrya on growth, photosynthesis, light absorption, and quantum yield of bloom-forming dinoflagellates
inferred← citeshttps://doi.org/10.3354/meps239057openalex-snapshot
Top-down regulation in ctenophore-copepod-ciliate-diatom-phytoflagellate communities in coastal waters: a mesocosm study
inferred← citeshttps://doi.org/10.3354/meps262137openalex-snapshot
Feeding in the mixotrophic dinoflagellate Ceratium furca is influenced by intracellular nutrient concentrations
inferred← citeshttps://doi.org/10.3389/fmars.2023.1296836openalex-snapshot
Morphology of Hobagella saltata n. gen. and n. sp. (Syndiniophyceae, Miozoa) infecting the marine dinoflagellate Cucumeridinium coeruleum (Dinophyceae, Miozoa) and its potential onshore advection
inferred← citeshttps://doi.org/10.3390/d14020070openalex-snapshot
Morphology and Molecular Phylogeny of Fuscheriides baugilensis sp. nov. (Protozoa, Ciliophora, Haptorida) from South Korea
inferred← citeshttps://doi.org/10.3390/microorganisms10050913openalex-snapshot
Diversity Patterns of Protists Are Highly Affected by Methods Disentangling Biological Variants: A Case Study in Oligotrich (s.l.) Ciliates
inferred← citeshttps://doi.org/10.3923/ajava.2013.663.669openalex-snapshot
An Investigation into Marine Ciliates with Establishment of a New Genus, Phyllopharyngean americana Nov. Gen., Nov. Spec.
inferred← citeshttps://doi.org/10.4467/16890027ap.26.002.23471openalex-snapshot
250 years of Tintinnid Studies: Modern Era Workers
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