On the public citation graph
Mixotrophy in the nematocyst–taeniocyst complex-bearing phototrophic dinoflagellate Polykrikos hartmannii
0 signed · 92 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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/10.1007/s11120-010-9546-8openalex-snapshot
The acquisition of phototrophy: adaptive strategies of hosting endosymbionts and organelles
inferredcites →https://doi.org/10.1007/s12237-009-9169-5openalex-snapshot
Understanding Causes and Impacts of the Dinoflagellate, Cochlodinium polykrikoides, Blooms in the Chesapeake Bay
inferredcites →https://doi.org/10.1007/s12601-010-0007-2openalex-snapshot
Growth, feeding and ecological roles of the mixotrophic and heterotrophic dinoflagellates in marine planktonic food webs
inferredcites →https://doi.org/10.1007/s12601-013-0001-6openalex-snapshot
Morphology and molecular characterization of the epiphytic dinoflagellate Prorocentrum cf. rhathymum in temperate waters off Jeju Island, Korea
inferredcites →https://doi.org/10.1016/0025-326x(82)90024-8openalex-snapshot
Marine dinoflagellates of the British Isles
inferredcites →https://doi.org/10.1016/0041-0101(89)90017-2openalex-snapshot
Paralytic shellfish poisoning in northwest Spain: The toxicity of the dinoflagellate Gymnodinium catenatum
inferredcites →https://doi.org/10.1016/j.ejop.2009.08.003openalex-snapshot
Re-classification of Pheopolykrikos hartmannii as Polykrikos (Dinophyceae) based partly on the ultrastructure of complex extrusomes
inferredcites →https://doi.org/10.1016/j.hal.2007.12.004openalex-snapshot
Control of the harmful alga Cochlodinium polykrikoides by the naked ciliate Strombidinopsis jeokjo in mesocosm enclosures
inferredcites →https://doi.org/10.1016/j.hal.2007.12.006openalex-snapshot
Characterization, dynamics, and ecological impacts of harmful Cochlodinium polykrikoides blooms on eastern Long Island, NY, USA
inferredcites →https://doi.org/10.1016/j.hal.2008.08.010openalex-snapshot
Mixotrophy, a major mode of nutrition for harmful algal species in eutrophic waters
inferredcites →https://doi.org/10.1016/j.hal.2013.05.006openalex-snapshot
Morphology and molecular characterization of the epiphytic benthic dinoflagellate Ostreopsis cf. ovata in the temperate waters off Jeju Island, Korea
inferredcites →https://doi.org/10.1016/j.hal.2013.10.004openalex-snapshot
Mixotrophic dinoflagellate red tides in Korean waters: Distribution and ecophysiology
inferredcites →https://doi.org/10.1016/j.hal.2013.10.008openalex-snapshot
Red tides in Masan Bay, Korea in 2004–2005: I. Daily variations in the abundance of red-tide organisms and environmental factors
inferredcites →https://doi.org/10.1016/j.hal.2013.10.012openalex-snapshot
Economic impact, management and mitigation of red tides in Korea
inferredcites →https://doi.org/10.1016/j.hal.2015.06.004openalex-snapshot
A hierarchy of conceptual models of red-tide generation: Nutrition, behavior, and biological interactions
inferredcites →https://doi.org/10.1016/j.protis.2006.12.001openalex-snapshot
Morphology and Phylogeny of the Pseudocolonial Dinoflagellates Polykrikos lebourae and Polykrikos herdmanae n. sp.
inferredcites →https://doi.org/10.1016/j.protis.2013.12.001openalex-snapshot
Polykrikos tanit sp. nov., a New Mixotrophic Unarmoured Pseudocolonial Dinoflagellate from the NW Mediterranean Sea
inferredcites →https://doi.org/10.1046/j.1529-8817.2000.98076.xopenalex-snapshot
Mixotrophy in gyrodinium galatheanum (DINOPHYCEAE): grazing responses to light intensity and inorganic nutrients*
inferredcites →https://doi.org/10.1073/pnas.1204302109openalex-snapshot
Heterotrophic feeding as a newly identified survival strategy of the dinoflagellate Symbiodinium
inferredcites →https://doi.org/10.1093/plankt/8.4.811openalex-snapshot
Cyst and motile morphology of a colonial dinoflagellate Pheopolykrikos hartmannii (Zinunermann) comb. nov.
inferredcites →https://doi.org/10.1093/plankt/fbh114openalex-snapshot
Spatial and temporal patterns of phytoplankton composition in subtropical coastal lagoon, the Indian River Lagoon, Florida, USA
inferredcites →https://doi.org/10.1111/j.1440-1835.2008.00489.xopenalex-snapshot
Research Note: Molecular phylogenetic affiliations of Dissodinium pseudolunula, Pheopolykrikos hartmannii, Polykrikos cf. schwartzii and Polykrikos kofoidii to Gymnodinium sensu stricto species (Dinophyceae)
inferredcites →https://doi.org/10.1111/j.1529-8817.1986.tb00021.xopenalex-snapshot
THECATE HETEROPHIC DINOFLAGELLATES: FEEDING BEHAVIOR AND MECHANISMS 1
inferredcites →https://doi.org/10.1111/j.1529-8817.2007.00319.xopenalex-snapshot
CHARACTER EVOLUTION IN POLYKRIKOID DINOFLAGELLATES1
inferredcites →https://doi.org/10.1111/j.1550-7408.1999.tb04586.xopenalex-snapshot
Growth and Grazing Rates of the Marine Planktonic Ciliate Strombidinopsis sp. on Red‐Tide and Toxic Dinoflagellates
inferredcites →https://doi.org/10.1111/j.1550-7408.1999.tb04619.xopenalex-snapshot
Mixotrophy among Dinoflagellates1
inferredcites →https://doi.org/10.1111/j.1550-7408.2001.tb00318.xopenalex-snapshot
Growth and Grazing Rates of the Heterotrophic Dinoflagellate Polykrikos kofoidii on Red‐Tide and Toxic Dinoflagellates
inferredcites →https://doi.org/10.1111/j.1550-7408.2004.tb00292.xopenalex-snapshot
Mixotrophy in the Phototrophic Harmful Alga Cochlodinium polykrikoides (Dinophycean): Prey Species, the Effects of Prey Concentration, and Grazing Impact
inferredcites →https://doi.org/10.1111/j.1550-7408.2004.tb00540.xopenalex-snapshot
Interactions between Planktonic Microalgae and Protozoan Grazers1
inferredcites →https://doi.org/10.1111/j.1550-7408.2009.00421.xopenalex-snapshot
Feeding by Phototrophic Red‐Tide Dinoflagellates on the Ubiquitous Marine Diatom Skeletonema costatum
inferredcites →https://doi.org/10.1111/j.1550-7408.2009.00448.xopenalex-snapshot
Feeding by the Newly Described Mixotrophic Dinoflagellate Paragymnodinium shiwhaense: Feeding Mechanism, Prey Species, and Effect of Prey Concentration
inferredcites →https://doi.org/10.1111/j.1550-7408.2009.00462.xopenalex-snapshot
Description of a New Planktonic Mixotrophic Dinoflagellate Paragymnodinium shiwhaense n. gen., n. sp. from the Coastal Waters off Western Korea: Morphology, Pigments, and Ribosomal DNA Gene Sequence
inferredcites →https://doi.org/10.1111/j.1550-7408.2011.00531.xopenalex-snapshot
Mixotrophy in the Newly Described Phototrophic Dinoflagellate Woloszynskia cincta from Western Korean Waters: Feeding Mechanism, Prey Species and Effect of Prey Concentration
inferredcites →https://doi.org/10.1111/j.1550-7408.2011.00580.xopenalex-snapshot
Feeding by the Newly Described, Nematocyst‐Bearing Heterotrophic Dinoflagellate Gyrodiniellum shiwhaense
inferredcites →https://doi.org/10.1111/jeu.12041openalex-snapshot
A Dinoflagellate Amylax triacantha with Plastids of the Cryptophyte Origin: Phylogeny, Feeding Mechanism, and Growth and Grazing Responses
inferredcites →https://doi.org/10.1111/jpy.12037openalex-snapshot
Life Cycle of the pseudocolonial dinoflagellatePolykrikos kofoidii(Gymnodiniales, Dinoflagellata)
inferredcites →https://doi.org/10.1111/jpy.12114openalex-snapshot
Morphology, phylogeny, dynamics, and ichthyotoxicity of P heopolykrikos hartmannii ( D inophyceae) isolates and blooms from N ew Y ork, USA
inferredcites →https://doi.org/10.1139/m62-029openalex-snapshot
STUDIES OF MARINE PLANKTONIC DIATOMS: I. CYCLOTELLA NANA HUSTEDT, AND DETONULA CONFERVACEA (CLEVE) GRAN.
inferredcites →https://doi.org/10.1515/bot.2000.004openalex-snapshot
Dinoflagellate Cysts in Recent Marine Sediments from SW India
inferredcites →https://doi.org/10.2216/i0031-8884-35-6-490.1openalex-snapshot
Engulfment of Ceratium spp. (Dinophyceae) by the thecate photosynthetic dinoflagellate Fragilidium subglobosum
inferredcites →https://doi.org/10.2216/i0031-8884-39-1-82.1openalex-snapshot
Observations of the feeding behavior and growth rates of the heterotrophic dinoflagellate Polykrikos kofoidii (Polykrikaceae, Dinophyceae)
inferredcites →https://doi.org/10.2307/1539198openalex-snapshot
THE TAXONOMY OF UNARMORED DINOPHYCEAE OF SHALLOW EMBAYMENTS ON CAPE COD, MASSACHUSETTS
inferredcites →https://doi.org/10.3354/ame01166openalex-snapshot
Prey size spectrum and bioenergetics of the mixotrophic dinoflagellate Karlodinium armiger
inferredcites →https://doi.org/10.3354/ame01203openalex-snapshot
Growth and grazing responses of the mixotrophic dinoflagellate Dinophysis acuminata as functions of light intensity and prey concentration
inferredcites →https://doi.org/10.3354/ame01279openalex-snapshot
Grazing by Karenia brevis on Synechococcus enhances its growth rate and may help to sustain blooms
inferredcites →https://doi.org/10.3354/ame01394openalex-snapshot
Ecology of Gymnodinium aureolum. I. Feeding in western Korean waters
inferredcites →https://doi.org/10.3354/ame031307openalex-snapshot
Reduction in the toxicity of the dinoflagellate Gymnodinium catenatum when fed on by the heterotrophic dinoflagellate Polykrikos kofoidii
inferredcites →https://doi.org/10.3354/ame038249openalex-snapshot
Feeding by the mixotrophic red-tide dinoflagellate Gonyaulax polygramma: mechanisms, prey species, effects of prey concentration, and grazing impact
inferredcites →https://doi.org/10.3354/ame040133openalex-snapshot
Feeding by phototrophic red-tide dinoflagellates: five species newly revealed and six species previously known to be mixotrophic
inferredcites →https://doi.org/10.3354/ame041131openalex-snapshot
Feeding by red-tide dinoflagellates on the cyanobacterium Synechococcus
inferredcites →https://doi.org/10.3354/ame045101openalex-snapshot
First successful culture of the marine dinoflagellate Dinophysis acuminata
inferredcites →https://doi.org/10.3354/meps147187openalex-snapshot
Mixotrophic feeding of Fragilidium subglobosum (Dinophyceae) on three species of Ceratium:effects of prey concentration, prey species and light intensity
inferredcites →https://doi.org/10.3354/meps152001openalex-snapshot
Mixotrophy in the dinoflagellate Prorocentrum minimum
inferredcites →https://doi.org/10.3354/meps176263openalex-snapshot
Feeding by the mixotrophic thecate dinoflagellate Fragilidium cf. mexicanum on red-tide and toxic dinoflagellates
inferredcites →https://doi.org/10.3354/meps322085openalex-snapshot
Bacterivory by co-occurring red-tide algae, heterotrophic nanoflagellates, and ciliates
inferredcites →https://doi.org/10.37543/oceanides.v27i1.111openalex-snapshot
A checklist and classification of living dinoflagellates (Dinoflagellata, Alveolata)
inferredcites →https://doi.org/10.4319/lo.1972.17.6.0805openalex-snapshot
EFFECTS OF SIZE AND CONCENTRATION OF FOOD PARTICLES ON THE FEEDING BEHAVIOR OF THE MARINE PLANKTONIC COPEPOD CALANUS PACIFICUS 1
inferredcites →https://doi.org/10.4319/lo.1997.42.4.0687openalex-snapshot
Zooplankton grazing and growth: Scaling within the 2‐2,‐μm body size range
inferredcites →https://doi.org/10.4319/lo.1997.42.5_part_2.1137openalex-snapshot
Harmful algal blooms: Their ecophysiology and general relevance to phytoplankton blooms in the sea
inferredcites →https://doi.org/10.4319/lo.2000.45.3.0569openalex-snapshot
Carbon to volume relationships for dinoflagellates, diatoms, and other protist plankton
inferredcites →https://doi.org/10.4490/algae.2013.28.3.213openalex-snapshot
Morphology and molecular characterization of the epiphytic dinoflagellate Amphidinium massartii, isolated from the temperate waters off Jeju Island, Korea
inferredcites →https://doi.org/10.4490/algae.2014.29.2.137openalex-snapshot
Mixotrophy in the newly described dinoflagellate Ansanella granifera: feeding mechanism, prey species, and effect of prey concentration
inferredcites →https://doi.org/10.4490/algae.2014.29.2.153openalex-snapshot
Feeding by common heterotrophic dinoflagellates and a ciliate on the red-tide ciliate Mesodinium rubrum
inferredcites →https://doi.org/10.4490/algae.2015.30.1.035openalex-snapshot
Obligate mixotrophy of the pigmented dinoflagellate Polykrikos lebourae (Dinophyceae, Dinoflagellata)
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4846337openalex-extracted
First Bloom Report of Polykrikos Hartmannii (Dinophyceae), a Harmful Algal Bloom (Hab) Species in the Coastal Waters of the İzmir Bay (Aegean Sea, Eastern Mediterranean Sea)
inferred← citeshttps://doi.org/10.1002/lno.12708openalex-snapshot
Prey morphotype and abundance controls plastid retention and bloom dynamics for a mixotrophic dinoflagellate
inferred← citeshttps://doi.org/10.1007/s00227-025-04704-6openalex-snapshot
Mixotrophy in Pyrophacus horologium (thecate dinoflagellate): predation on toxic and harmful dinoflagellates and molecular phylogenetics
inferred← citeshttps://doi.org/10.1007/s00248-026-02739-wopenalex-snapshot
Feeding and growth of the new mixotrophic dinoflagellate Gymnodinium sp. GSTY2405 and the prey spectrum extension of its sister species Gymnodinium smaydae
inferred← citeshttps://doi.org/10.1007/s00709-016-0999-2openalex-snapshot
On the extrusomes of Oxyrrhis marina (Dinophyceae)
inferred← citeshttps://doi.org/10.1007/s10311-022-01457-2openalex-snapshot
Methods to control harmful algal blooms: a review
inferred← citeshttps://doi.org/10.1016/j.hal.2016.09.008openalex-snapshot
Mixotrophic ability of the phototrophic dinoflagellates Alexandrium andersonii, A. affine, and A. fraterculus
inferred← citeshttps://doi.org/10.1016/j.hal.2016.10.008openalex-snapshot
Mixotrophy in the phototrophic dinoflagellate Takayama helix (family Kareniaceae): Predator of diverse toxic and harmful dinoflagellates
inferred← citeshttps://doi.org/10.1016/j.hal.2016.12.005openalex-snapshot
Differential interactions between the nematocyst-bearing mixotrophic dinoflagellate Paragymnodinium shiwhaense and common heterotrophic protists and copepods: Killer or prey
inferred← citeshttps://doi.org/10.1016/j.hal.2016.12.007openalex-snapshot
Mixotrophy in the newly described dinoflagellate Yihiella yeosuensis : A small, fast dinoflagellate predator that grows mixotrophically, but not autotrophically
inferred← citeshttps://doi.org/10.1016/j.hal.2020.101846openalex-snapshot
Allelopathic effects of Margalefidinium polykrikoides and Gymnodinium impudicum in the growth of Gymnodinium catenatum
inferred← citeshttps://doi.org/10.1016/j.marmicro.2017.05.004openalex-snapshot
Atlas of modern dinoflagellate cyst distributions in the Black Sea Corridor: from Aegean to Aral Seas, including Marmara, Black, Azov and Caspian Seas
inferred← citeshttps://doi.org/10.1038/s41598-018-37065-wopenalex-snapshot
Dinoflagellate nucleus contains an extensive endomembrane network, the nuclear net
inferred← citeshttps://doi.org/10.1080/17451000.2017.1379604openalex-snapshot
Mixotrophy in the sand-dwelling dinoflagellate Thecadinium kofoidii
inferred← citeshttps://doi.org/10.1111/jpy.12525openalex-snapshot
The function of the ocelloid and piston in the dinoflagellate Erythropsidinium (Gymnodiniales, Dinophyceae)
inferred← citeshttps://doi.org/10.1111/jpy.12981openalex-snapshot
Ultrastructure and Systematics of Two New Species of Dinoflagellate, Paragymnodinium Asymmetricum sp. nov. and Paragymnodinium Inerme sp. nov. (Gymnodiniales, Dinophyceae) 1
inferred← citeshttps://doi.org/10.1111/jpy.70201openalex-snapshot
Revisiting the life cycle of Margalefidinium polykrikoides Group III
inferred← citeshttps://doi.org/10.1111/pre.12452openalex-snapshot
Paragymnodinium verecundum sp. nov. (Gymnodiniales, Dinophyceae), a new species of mixotrophic dinoflagellate from Japan
inferred← citeshttps://doi.org/10.1126/sciadv.1602552openalex-snapshot
Microbial arms race: Ballistic “nematocysts” in dinoflagellates represent a new extreme in organelle complexity
inferred← citeshttps://doi.org/10.3389/fmars.2024.1354063openalex-snapshot
Rapid dilution effectively decreases hydrocarbons following small oil spills, but impacts on microeukaryote communities are still observed
inferred← citeshttps://doi.org/10.4490/algae.2016.31.11.17openalex-snapshot
Reduction in CO2 uptake rates of red tide dinoflagellates due to mixotrophy
inferred← citeshttps://doi.org/10.4490/algae.2017.32.11.27openalex-snapshot
Interactions between the voracious heterotrophic nanoflagellate Katablepharis japonica and common heterotrophic protists
inferred← citeshttps://doi.org/10.4490/algae.2017.32.11.28openalex-snapshot
Ichthyotoxic Cochlodinium polykrikoides red tides offshore in the South Sea, Korea in 2014: III. Metazooplankton and their grazing impacts on red-tide organisms and heterotrophic protists
inferred← citeshttps://doi.org/10.4490/algae.2017.32.8.25openalex-snapshot
Ichthyotoxic Cochlodinium polykrikoides red tides offshore in the South Sea, Korea in 2014: II. Heterotrophic protists and their grazing impacts on red-tide organisms
inferred← citeshttps://doi.org/10.4490/algae.2020.35.2.24openalex-snapshot
Spatio-temporal distributions of the newly described mixotrophic dinoflagellate Yihiella yeosuensis (Suessiaceae) in Korean coastal waters and its grazing impact on prey populations
inferred← citeshttps://doi.org/10.4490/algae.2023.38.12.6openalex-snapshot
Protists in hypoxic waters of Jinhae Bay and Masan Bay, Korea, based on metabarcoding analyses: emphasizing surviving dinoflagellates
inferred← citeshttps://doi.org/10.4490/algae.2023.38.6.6openalex-snapshot
Five phototrophic Scrippsiella species lacking mixotrophic ability and the extended prey spectrum of Scrippsiella acuminata (Thoracosphaerales, Dinophyceae)
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.