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Towards an Ecological Understanding of Dinoflagellate Cyst Functions
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/jqs.2564openalex-snapshot
Process length variation of the cyst of the dinoflagellate Protoceratium reticulatum in the North Pacific and Baltic‐Skagerrak region: calibration as an annual density proxy and first evidence of pseudo‐cryptic speciation
inferredcites →https://doi.org/10.1007/978-1-4020-4443-4_14openalex-snapshot
Biomacromolecules of algae and plants and their fossil analogues
inferredcites →https://doi.org/10.1007/978-94-017-1907-0_17openalex-snapshot
Morphological convergence of resting stages of planktonic organisms: a review
inferredcites →https://doi.org/10.1007/bf00350743openalex-snapshot
Mass encystment and sinking of dinoflagellates during a spring bloom
inferredcites →https://doi.org/10.1007/bf00626331openalex-snapshot
Sexualität beiCeratium cornutum (Dinophyta)
inferredcites →https://doi.org/10.1007/s00227-007-0652-xopenalex-snapshot
Temporary cyst enables long-term dark survival of Scrippsiella hangoei (Dinophyceae)
inferredcites →https://doi.org/10.1007/s11258-005-9027-xopenalex-snapshot
Biomacromolecules of Algae and Plants and their Fossil Analogues
inferredcites →https://doi.org/10.1016/0022-0981(85)90039-5openalex-snapshot
Time-course measurements of phosphorus depletion and cyst formation in the dinoflagellate Gonyaulax tamarensis Lebour
inferredcites →https://doi.org/10.1016/0303-2647(80)90006-4openalex-snapshot
On dinoflagellate evolution
inferredcites →https://doi.org/10.1016/b978-0-12-656520-1.50017-1openalex-snapshot
Dinoflagellate Cysts
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The intricacies of dinoflagellate pellicle cysts: The example of Alexandrium minutum cysts from a bloom-recurrent area (Bay of Baiona, NW Spain)
inferredcites →https://doi.org/10.1016/j.dsr2.2009.09.004openalex-snapshot
Bloom dynamics and life cycle strategies of two toxic dinoflagellates in a coastal upwelling system (NW Iberian Peninsula)
inferredcites →https://doi.org/10.1016/j.ecss.2004.07.008openalex-snapshot
Breeze conditions as a favoring mechanism of Alexandrium taylori blooms at a Mediterranean beach
inferredcites →https://doi.org/10.1016/j.hal.2012.02.001openalex-snapshot
Viability of Alexandrium tamarense cysts in the sediment of Funka Bay, Hokkaido, Japan: Over a hundred year survival times for cysts
inferredcites →https://doi.org/10.1016/j.hal.2012.04.001openalex-snapshot
Life cycle stages of the benthic palytoxin-producing dinoflagellate Ostreopsis cf. ovata (Dinophyceae)
inferredcites →https://doi.org/10.1016/j.marmicro.2008.10.004openalex-snapshot
Process length variation in cysts of a dinoflagellate, Lingulodinium machaerophorum, in surface sediments: Investigating its potential as salinity proxy
inferredcites →https://doi.org/10.1016/j.orggeochem.2004.06.012openalex-snapshot
An example of oxidative polymerization of unsaturated fatty acids as a preservation pathway for dinoflagellate organic matter
inferredcites →https://doi.org/10.1016/j.orggeochem.2011.10.007openalex-snapshot
Infra red spectroscopy, flash pyrolysis, thermally assisted hydrolysis and methylation (THM) in the presence of tetramethylammonium hydroxide (TMAH) of cultured and sediment-derived Lingulodinium polyedrum (Dinoflagellata) cyst walls
inferredcites →https://doi.org/10.1016/j.pocean.2010.02.006openalex-snapshot
Dinoflagellate blooms in upwelling systems: Seeding, variability, and contrasts with diatom bloom behaviour
inferredcites →https://doi.org/10.1016/j.protis.2005.09.002openalex-snapshot
The Systematic Position of the Parasitoid Marine Dinoflagellate Paulsenella vonstoschii (Dinophyceae) Inferred from Nuclear-Encoded Small Subunit Ribosomal DNA
inferredcites →https://doi.org/10.1016/j.protis.2008.05.003openalex-snapshot
Description, Host-specificity, and Strain Selectivity of the Dinoflagellate Parasite Parvilucifera sinerae sp. nov. (Perkinsozoa)
inferredcites →https://doi.org/10.1016/j.protis.2008.12.003openalex-snapshot
The Life History and Cell Cycle of Kryptoperidinium foliaceum, A Dinoflagellate with Two Eukaryotic Nuclei
inferredcites →https://doi.org/10.1016/j.protis.2010.12.001openalex-snapshot
Interplay Between the Parasite Amoebophrya sp. (Alveolata) and the Cyst Formation of the Red Tide Dinoflagellate Scrippsiella trochoidea
inferredcites →https://doi.org/10.1016/j.revpalbo.2006.09.001openalex-snapshot
Effects of temperature, light and salinity on cyst production and morphology of Tuberculodinium vancampoae (the resting cyst of Pyrophacus steinii)
inferredcites →https://doi.org/10.1016/s0003-9365(79)80022-6openalex-snapshot
Elektronenmikroskopische Untersuchungen am Panzer von Dinoflagellaten
inferredcites →https://doi.org/10.1016/s0022-0981(02)00549-xopenalex-snapshot
Viability of dinoflagellate cysts after the passage through the copepod gut
inferredcites →https://doi.org/10.1016/s0146-6380(97)00134-4openalex-snapshot
Characterization of a highly resistant biomacromolecular material in the cell wall of a marine dinoflagellate resting cyst
inferredcites →https://doi.org/10.1021/bk-1984-0262.ch011openalex-snapshot
Shellfish Toxicity and Dormant Cysts in Toxic Dinoflagellate Blooms
inferredcites →https://doi.org/10.1023/a:1003071205424openalex-snapshot
Morphological convergence of resting stages of planktonic organisms: a review
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Effects of particle shape on settling velocity at low Reynolds numbers
inferredcites →https://doi.org/10.1038/325616a0openalex-snapshot
An endogenous annual clock in the toxic marine dinoflagellate Gonyaulax tamarensis
inferredcites →https://doi.org/10.1038/ncomms1314openalex-snapshot
Phytoplankton growth after a century of dormancy illuminates past resilience to catastrophic darkness
inferredcites →https://doi.org/10.1038/sj.hdy.6800034openalex-snapshot
Origins of the machinery of recombination and sex
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ENVIRONMENTAL AND ENDOGENOUS REGULATION OF CYST GERMINATION IN TWO FRESHWATER DINOFLAGELLATES
inferredcites →https://doi.org/10.1046/j.1529-8817.2002.01062.xopenalex-snapshot
CYST–THECA RELATIONSHIP, LIFE CYCLE, AND EFFECTS OF TEMPERATURE AND SALINITY ON THE CYST MORPHOLOGY OF GONYAULAX BALTICA SP. NOV. (DINOPHYCEAE) FROM THE BALTIC SEA AREA1
inferredcites →https://doi.org/10.1046/j.1529-8817.2002.01242.xopenalex-snapshot
LIFE CYCLE OF THE HETEROTROPHIC DINOFLAGELLATE PFIESTERIA PISCICIDA (DINOPHYCEAE)1
inferredcites →https://doi.org/10.1051/alr:2007015openalex-snapshot
Viability, growth and toxicity ofAlexandrium catenellaandAlexandrium minutum(Dinophyceae) following ingestion and gut passage in the oysterCrassostrea gigas
inferredcites →https://doi.org/10.1080/00071617200650111openalex-snapshot
The encystment of a freshwater dinoflagellate: A light and electron-microscopical study
inferredcites →https://doi.org/10.1080/00071617300650141openalex-snapshot
Observations on vegetative reproduction and sexual life cycles of two freshwater dinoflagellates,Gymondinium pseudopalustreSchiller andWoloszynskia apiculatasp. nov.
inferredcites →https://doi.org/10.1080/00071618900650151openalex-snapshot
An ultrastructural study of planozygotes and encystment of a marine dinoflagellate,Scrippsiellasp
inferredcites →https://doi.org/10.1080/00139307509435842openalex-snapshot
Implications of Dinoflagellate Life Cycles on Initiation ofGymnodinium BreveRed Tides
inferredcites →https://doi.org/10.1080/00173136509429150openalex-snapshot
Modern Hystrichospheres and Dinoflagellate Cysts from the Woods Hole Region
inferredcites →https://doi.org/10.1080/00288330.2012.719911openalex-snapshot
The first report of Vulcanodinium rugosum (Dinophyceae) from the South China Sea with a focus on the life cycle
inferredcites →https://doi.org/10.1080/00364827.1977.10411318openalex-snapshot
Cysts of the toxic red-tide dinoflagellateGonyaulax excavata(Braarud) Balech from Oslofjorden, Norway
inferredcites →https://doi.org/10.1080/00378941.1972.10839089openalex-snapshot
La signification cytologique de la « cyclose nucléaire » dans le cycle de vie des Dinoflagellés
inferredcites →https://doi.org/10.1080/00721395.1971.9989704openalex-snapshot
Biological problems concerning fossilizable dinoflagellates
inferredcites →https://doi.org/10.1080/01916122.1995.9989457openalex-snapshot
Morphological development of resting cysts in cultures of the marine dinoflagellateLingulodinium polyedrum(=L. Machaerophorum)
inferredcites →https://doi.org/10.1080/09670260600810360openalex-snapshot
Resting cysts of the toxigenic dinoflagellate genusAlexandriumin recent sediments from the Western Mediterranean coast, including the first description of cysts ofA. kutneraeandA. peruvianum
inferredcites →https://doi.org/10.1080/11035895009454146openalex-snapshot
Fynd av Hystrichosphaera furcata i Gullmarn
inferredcites →https://doi.org/10.1093/aob/mcs194openalex-snapshot
Seed dormancy distribution: explanatory ecological factors
inferredcites →https://doi.org/10.1093/genetics/156.1.423openalex-snapshot
The Evolution of Recombination in a Heterogeneous Environment
inferredcites →https://doi.org/10.1093/plankt/16.5.513openalex-snapshot
The effects of temperature, growth medium and darkness on excystment and growth of the toxic dinoflagellate Gymnodinium catenatum from northwest Spain
inferredcites →https://doi.org/10.1093/plankt/18.10.1837openalex-snapshot
Influences of temperature, salinity and irradiance on growth of Prorocentrum minimum (Dinophyceae) from the Mediterranean Sea
inferredcites →https://doi.org/10.1093/plankt/21.12.2373openalex-snapshot
A recurrent and localized dinoflagellate bloom in a Mediterranean beach
inferredcites →https://doi.org/10.1093/plankt/22.7.1311openalex-snapshot
Factors regulating germination of resting cysts of the spring bloom dinoflagellate Scrippsiella hangoei from the northern Baltic Sea
inferredcites →https://doi.org/10.1093/plankt/24.7.681openalex-snapshot
Role of temporary cysts in the population dynamics of Alexandrium taylori (Dinophyceae)
inferredcites →https://doi.org/10.1093/plankt/fbi149openalex-snapshot
Vertical distribution and cyst production of Peridiniella catenata (Dinophyceae) during a spring bloom in the Baltic Sea
inferredcites →https://doi.org/10.1093/plankt/fbm034openalex-snapshot
On the allelochemical potency of the marine dinoflagellate Alexandrium ostenfeldii against heterotrophic and autotrophic protists
inferredcites →https://doi.org/10.1098/rspb.2003.2654openalex-snapshot
Marine dinoflagellates show induced life-history shifts to escape parasite infection in response to water–borne signals
inferredcites →https://doi.org/10.1111/j.0022-3646.1985.00200.xopenalex-snapshot
ENCYSTMENT OF THE DINOFLAGELLATEGYRODINIUM UNCATENUM: TEMPERATURE AND NUTRIENT EFFECTS1
inferredcites →https://doi.org/10.1111/j.0022-3646.1989.00095.xopenalex-snapshot
ULTRASTRUCTURAL ASPECTS OF SEXUAL REPRODUCTION IN THE RED TIDE DINOFLAGELLATEGONYAULAX TAMARENSIS1
inferredcites →https://doi.org/10.1111/j.0022-3646.1992.00082.xopenalex-snapshot
AMPHIESMAL ULTRASTRUCTURE OF DINOFLAGELLATES: A REEVALUATION OF PELLICLE FORMATION1
inferredcites →https://doi.org/10.1111/j.1365-294x.2009.04165.xopenalex-snapshot
Implications of life‐history transitions on the population genetic structure of the toxigenic marine dinoflagellate Alexandrium tamarense
inferredcites →https://doi.org/10.1111/j.1440-1835.1996.tb00040.xopenalex-snapshot
The life cycle of Gyrodinium instriatum (Dinophyceae) in culture*
inferredcites →https://doi.org/10.1111/j.1462-2920.2004.00609.xopenalex-snapshot
Temporary cyst formation in phytoplankton: a response to allelopathic competitors?
inferredcites →https://doi.org/10.1111/j.1529-8817.1978.tb02452.xopenalex-snapshot
POTENTIAL IMPORTANCE OF BENTHIC CYSTS OF GONYAULAX TAMARENSIS AND G. EXCAVATA IN INITIATING TOXIC DINOFLAGELLATE BLOOMS 1, 2, 3
inferredcites →https://doi.org/10.1111/j.1529-8817.1980.tb03013.xopenalex-snapshot
EFFECTS OF TEMPERATURE CONDITIONING ON DEVELOPMENT AND GERMINATION OFGONYAULAX TAMARENSIS(DINOPHYCEAE) HYPNOZYGOTES1
inferredcites →https://doi.org/10.1111/j.1529-8817.1981.tb00857.xopenalex-snapshot
THE DINOFLAGELLATE PELLICULAR WALL LAYER AND ITS OCCURRENCE IN THE DIVISION PYRRHOPHYTA1
inferredcites →https://doi.org/10.1111/j.1529-8817.1982.tb03165.xopenalex-snapshot
CYST FORMATION IN THE FRESHWATER DINOFLAGELLATE CERATIUM HIRUNDINELLA (DINOPHYCEAE)1
inferredcites →https://doi.org/10.1111/j.1529-8817.2004.03202.xopenalex-snapshot
THE SEXUAL LIFE CYCLES OF PFIESTERIA PISCICIDA AND CRYPTOPERIDINIOPSOIDS (DINOPHYCEAE)1
inferredcites →https://doi.org/10.1111/j.1529-8817.2005.04045.xopenalex-snapshot
A STUDY OF THE SEXUAL REPRODUCTION AND DETERMINATION OF MATING TYPE OF GYMNODINIUM NOLLERI (DINOPHYCEAE) IN CULTURE1
inferredcites →https://doi.org/10.1111/j.1529-8817.2005.04150.xopenalex-snapshot
SEXUAL REPRODUCTION AND TWO DIFFERENT ENCYSTMENT STRATEGIES OF LINGULODINIUM POLYEDRUM (DINOPHYCEAE) IN CULTURE 1
inferredcites →https://doi.org/10.1111/j.1529-8817.2006.00181.xopenalex-snapshot
NUCLEAR FEATURES AND EFFECT OF NUTRIENTS ON GYMNODINIUM CATENATUM (DINOPHYCEAE) SEXUAL STAGES 1
inferredcites →https://doi.org/10.1111/j.1529-8817.2006.00191.xopenalex-snapshot
EFFECTS OF PARENTAL FACTORS AND MEIOSIS ON SEXUAL OFFSPRING OF GYMNODINIUM NOLLERI (DINOPHYCEAE)1
inferredcites →https://doi.org/10.1111/j.1529-8817.2006.00205.xopenalex-snapshot
EVIDENCE FOR ASEXUAL RESTING CYSTS IN THE LIFE CYCLE OF THE MARINE PERIDINOID DINOFLAGELLATE,SCRIPPSIELLA HANGOEI1
inferredcites →https://doi.org/10.1111/j.1529-8817.2006.00262.xopenalex-snapshot
MULTIPLE ROUTES OF SEXUALITY INALEXANDRIUM TAYLORI(DINOPHYCEAE) IN CULTURE1
inferredcites →https://doi.org/10.1111/j.1529-8817.2007.00393.xopenalex-snapshot
Comparative study of the life cycles of Alexandrium tamutum and Alexandrium minutum (Gonyaulacales, Dinophyceae) in culture1
inferredcites →https://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)
inferredcites →https://doi.org/10.1128/mmbr.00005-10openalex-snapshot
The Evolution of Sex: a Perspective from the Fungal Kingdom
inferredcites →https://doi.org/10.1371/journal.pone.0061075openalex-snapshot
Co-Variation between Seed Dormancy, Growth Rate and Flowering Time Changes with Latitude in Arabidopsis thaliana
inferredcites →https://doi.org/10.2216/0031-8884(2005)44[416:sowdiw]2.0.co;2openalex-snapshot
Studies on woloszynskioid dinoflagellates I:Woloszynskia coronatare-examined using light and electron microscopy and partial LSU rDNA sequences, with description ofTovelliagen. nov. andJadwigiagen. nov. (Tovelliaceae fam. nov.)
inferredcites →https://doi.org/10.2216/0031-8884(2005)44[658:eonfad]2.0.co;2openalex-snapshot
Effects of nutritional factors and different parental crosses on the encystment and excystment of Alexandrium catenella (Dinophyceae) in culture
inferredcites →https://doi.org/10.2216/11-16.1openalex-snapshot
Buried alive – germination of up to a century-old marine protist resting stages
inferredcites →https://doi.org/10.2216/i0031-8884-27-3-413.1openalex-snapshot
Alternate life history stages in Amphidinium klebsii (Dinophyceae, Pyrrophyta)
inferredcites →https://doi.org/10.2216/i0031-8884-41-6-667.1openalex-snapshot
Regeneration from hyaline cysts of Cochlodinium polykrikoides (Gymnodiniales, Dinophyceae), a red tide organism along the Korean coast
inferredcites →https://doi.org/10.2216/i0031-8884-43-4-355.1openalex-snapshot
An ultrastructural study of hypnozygotes of Alexandrium species (Dinophyceae)
inferredcites →https://doi.org/10.2307/1308678openalex-snapshot
Biologic and Hydrographic Aspects of Red Tides
inferredcites →https://doi.org/10.2307/1484378openalex-snapshot
Observations on the Morphology of Fossil Dinoflagellates
inferredcites →https://doi.org/10.2307/2260522openalex-snapshot
The Ecology of Freshwater Phytoplankton.
inferredcites →https://doi.org/10.2307/2420042openalex-snapshot
The Structure and Reproduction of the Algae.
inferredcites →https://doi.org/10.2331/suisan.57.1215openalex-snapshot
Sexual Reproduction of Scrippsiella trochoidea Isolated from Muroran Harbor, Hokkaido
inferredcites →https://doi.org/10.2331/suisan.57.2249openalex-snapshot
Life-Cycle and Its Control of Sargassum muticum (Phaeophyta) in Batch Cultures.
inferredcites →https://doi.org/10.3354/ame01206openalex-snapshot
New life-cycle stages of Gymnodinium catenatum (Dinophyceae): laboratory and field observations
inferredcites →https://doi.org/10.3354/ame01497openalex-snapshot
Influence of altered light conditions and grazers on Scrippsiella trochoidea (Dinophyceae) cyst formation
inferredcites →https://doi.org/10.3354/meps216057openalex-snapshot
Effects of cyst resuspension on germination and seeding of two bloom-forming dinoflagellates in the Baltic Sea
inferredcites →https://doi.org/10.4319/lo.1985.30.5.1000openalex-snapshot
Sinking characteristics of dinoflagellate cysts1
inferredcites →https://doi.org/10.4319/lo.1987.32.2.0340openalex-snapshot
The effects of darkness and anaerobiosis on dinoflagellate cyst germination1,2
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Scrippsiella acuminata versus Scrippsiella ramonii: A Physiological Comparison
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Molecular cloning of heat shock protein 60 (Hsp60) and 10 (Hsp10) genes from the cosmopolitan and harmful dinoflagellate Scrippsiella trochoidea and their differential transcriptions responding to temperature stress and alteration of life cycle
inferred← citeshttps://doi.org/10.1007/s00227-019-3554-9openalex-snapshot
De novo transcriptome of the newly described phototrophic dinoflagellate Yihiella yeosuensis: comparison between vegetative cells and cysts
inferred← citeshttps://doi.org/10.1007/s00227-019-3569-2openalex-snapshot
Variation in biochemical composition during encystment of the planktonic dinoflagellate Akashiwo sanguinea in N-limited cultures
inferred← citeshttps://doi.org/10.1007/s00227-020-03774-yopenalex-snapshot
Variation in the photosynthetic activities of the dinoflagellate Akashiwo sanguinea during formation of resting cysts
inferred← citeshttps://doi.org/10.1007/s00248-023-02175-0openalex-snapshot
Contrasting Mechanisms Determine the Microeukaryotic and Syndiniales Community Assembly in a Eutrophic bay
inferred← citeshttps://doi.org/10.1007/s00343-018-6291-xopenalex-snapshot
Solid sand particle addition can enhance the production of resting cysts in dinoflagellates
inferred← citeshttps://doi.org/10.1007/s00343-019-9077-xopenalex-snapshot
Proof of homothally of Pheopolykrikos hartmannii and details of cyst germination process
inferred← citeshttps://doi.org/10.1007/s00343-022-2122-1openalex-snapshot
Reviving and characterizing three species of dinoflagellate cysts dormant for about 70 years in the East China Sea: Biecheleria brevisulcata, Biecheleriopsis adriatica, and Scrippsiella donghaienis
inferred← citeshttps://doi.org/10.1007/s00343-024-4134-5openalex-snapshot
Establishing an assessment framework for the risk of dinoflagellate HABs based on cyst-mapping of marine sediments
inferred← citeshttps://doi.org/10.1007/s00343-025-5021-4openalex-snapshot
Composition and distribution of dinoflagellate cysts in surficial sediments and their linkages to their free-living form in five bays of three eastern islands in the Philippines, western Pacific border
inferred← citeshttps://doi.org/10.1007/s00343-026-5157-xopenalex-snapshot
Cyst induction by intracellular Mg2+/Ca2+ injection and its implications for optimizing Mg2+ conditions for future CRISPR delivery in Alexandrium catenella
inferred← citeshttps://doi.org/10.1007/s10661-022-10451-8openalex-snapshot
Mobility of trace metals and microbiological pollution from dredged sediments to the Gulf of Gabes, Tunisia
inferred← citeshttps://doi.org/10.1007/s10750-016-2885-5openalex-snapshot
Introduction to the biology and ecology of the freshwater cryophilic dinoflagellate Woloszynskia pascheri causing red ice
inferred← citeshttps://doi.org/10.1007/s10811-018-1399-0openalex-snapshot
The ‘stress’ concept in microalgal biology—homeostasis, acclimation and adaptation
inferred← citeshttps://doi.org/10.1007/s10811-019-01809-6openalex-snapshot
Cloning and comparative studies of proliferating cell nuclear antigen (PCNA) genes for nine dinoflagellates
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A perspective on the current status of approaches for early detection of microalgal grazing
inferred← citeshttps://doi.org/10.1007/s10811-022-02862-4openalex-snapshot
Molecular cloning, origin, and expression of saxitoxin biosynthesis gene sxtB from the toxic dinoflagellate Alexandrium catenella
inferred← citeshttps://doi.org/10.1007/s11356-015-5526-zopenalex-snapshot
Microbenthic community structure and trophic status of sediments in the Mar Piccolo of Taranto (Mediterranean, Ionian Sea)
inferred← citeshttps://doi.org/10.1007/s11356-024-34451-yopenalex-snapshot
First insights into the distribution and diversity of toxic dinoflagellate cysts in the surface sediments of Dakhla Bay (African Atlantic coast): relationships with environmental factors and mollusk intoxication events
inferred← citeshttps://doi.org/10.1007/s11802-023-5583-8openalex-snapshot
Effects of 5-Azacytidine (AZA) on the Growth, Antioxidant Activities and Germination of Pellicle Cysts of Scrippsiella acuminata (Dinophyceae)
inferred← citeshttps://doi.org/10.1007/s12298-022-01228-xopenalex-snapshot
Responses of Prorocentrum cordatum (Ostenfeld) Dodge, 1975 (Dinoflagellata) to copper nanoparticles and copper ions effect
inferred← citeshttps://doi.org/10.1007/s12526-016-0523-0openalex-snapshot
A multidisciplinary approach to study confined marine basins: the holobenthic and merobenthic assemblages in the Mar Piccolo of Taranto (Ionian Sea, Mediterranean)
inferred← citeshttps://doi.org/10.1007/s12526-018-0850-4openalex-snapshot
Influence of environmental factors on spatial–temporal distribution patterns of dinoflagellate cyst communities in the South China Sea
inferred← citeshttps://doi.org/10.1007/s13131-016-0887-9openalex-snapshot
Validation of reference genes for gene expression studies in the dinoflagellate Akashiwo sanguinea by quantitative real-time RT-PCR
inferred← citeshttps://doi.org/10.1007/s13131-019-1375-9openalex-snapshot
The impact of biotic and abiotic factors on the distribution of surface sediment dinoflagellate cyst assemblages on the Nanji Island in the East China Sea
inferred← citeshttps://doi.org/10.1016/b978-0-12-811405-6.00003-7openalex-snapshot
Biology of Microalgae
inferred← citeshttps://doi.org/10.1016/b978-0-443-15743-1.00005-4openalex-snapshot
Sexual reproduction, cell cycle, and molecular regulators
inferred← citeshttps://doi.org/10.1016/j.ancene.2017.11.004openalex-snapshot
Algal palynomorphs as proxies of human impact on freshwater resources in the Great Lakes region
inferred← citeshttps://doi.org/10.1016/j.aquatox.2023.106732openalex-snapshot
Palmelloid-like phenotype in the alga Raphidocelis subcapitata exposed to pollutants: A generalized adaptive strategy to stress or a specific cellular response?
inferred← citeshttps://doi.org/10.1016/j.cretres.2017.04.003openalex-snapshot
Intrinsic processes control late Turonian calcareous dinoflagellate cyst assemblages – A case study from the Sussex chalk (England)
inferred← citeshttps://doi.org/10.1016/j.csr.2016.11.012openalex-snapshot
Spring bloom dinoflagellate cyst dynamics in three eastern sub-basins of the Baltic Sea
inferred← citeshttps://doi.org/10.1016/j.csr.2022.104648openalex-snapshot
Assemblages of dinoflagellate resistance cysts and copepod eggs in superficial sediments at the upper Gulf of California
inferred← citeshttps://doi.org/10.1016/j.dsr.2018.06.003openalex-snapshot
Transport of organic-walled dinoflagellate cysts in nepheloid layers off Cape Blanc (N-W Africa)
inferred← citeshttps://doi.org/10.1016/j.earscirev.2022.104172openalex-snapshot
Reply to the discussion paper by R. Martin on Kroeck et al. “A review of Paleozoic phytoplankton biodiversity: Driver for major evolutionary events?”
inferred← citeshttps://doi.org/10.1016/j.earscirev.2025.105280openalex-snapshot
Middle to Late Devonian calcium-stressed restricted-marine basins as a unique habitat and taphonomic window for calcareous microbiota
inferred← citeshttps://doi.org/10.1016/j.ecoinf.2025.103460openalex-snapshot
Recent advances in dinoflagellate cyst: Integrating review with visual taxonomic perspectives
inferred← citeshttps://doi.org/10.1016/j.ecolmodel.2014.02.015openalex-snapshot
Processes leading to the coexistence of a host and its parasitoid in homogeneous environments: The role of an infected dormant stage
inferred← citeshttps://doi.org/10.1016/j.ecss.2020.106648openalex-snapshot
Dinoflagellates encystment with emphasis on blooms in Boughrara Lagoon (South-Western Mediterranean): Combined effects of trace metal concentration and environmental context
inferred← citeshttps://doi.org/10.1016/j.ecss.2021.107239openalex-snapshot
Abiotic stability promotes dinoflagellate blooms in marine coastal ecosystems
inferred← citeshttps://doi.org/10.1016/j.ejop.2021.125770openalex-snapshot
Fine-structural characterization and phylogeny of Sphaerodinium (Suessiales, Dinophyceae), with the description of an unusual type of freshwater dinoflagellate cyst
inferred← citeshttps://doi.org/10.1016/j.envpol.2022.119901openalex-snapshot
The role of physico-chemical interactions in the seasonality of toxic dinoflagellate cyst assemblages: The case of the NW Patagonian fjords system
inferred← citeshttps://doi.org/10.1016/j.envpol.2023.121008openalex-snapshot
Response mechanism of harmful algae Phaeocystis globosa to ocean warming and acidification
inferred← citeshttps://doi.org/10.1016/j.hal.2014.08.005openalex-snapshot
Allelopathic activity of the toxic dinoflagellate Alexandrium ostenfeldii: Intra-population variability and response of co-occurring dinoflagellates
inferred← citeshttps://doi.org/10.1016/j.hal.2014.09.009openalex-snapshot
Cellular and nuclear morphological variability within a single species of the toxigenic dinoflagellate genus Gambierdiscus: Relationship to life-cycle processes
inferred← citeshttps://doi.org/10.1016/j.hal.2014.10.001openalex-snapshot
Coupling planktonic and benthic shifts during a bloom of Alexandrium catenella in southern Chile: Implications for bloom dynamics and recurrence
inferred← citeshttps://doi.org/10.1016/j.hal.2015.05.006openalex-snapshot
The effects of major environmental factors and nutrient limitation on growth and encystment of planktonic dinoflagellate Akashiwo sanguinea
inferred← citeshttps://doi.org/10.1016/j.hal.2015.05.009openalex-snapshot
Alexandrium and Scrippsiella cyst viability and cytoplasmic fullness in a 60-cm sediment core from Sequim Bay, WA
inferred← citeshttps://doi.org/10.1016/j.hal.2015.10.007openalex-snapshot
Differential expressions of an Hsp70 gene in the dinoflagellate Akashiwo sanguinea in response to temperature stress and transition of life cycle and its implications
inferred← citeshttps://doi.org/10.1016/j.hal.2016.06.004openalex-snapshot
Gambierdiscus balechii sp. nov (Dinophyceae), a new benthic toxic dinoflagellate from the Celebes Sea (SW Pacific Ocean)
inferred← citeshttps://doi.org/10.1016/j.hal.2016.10.005openalex-snapshot
Development of real-time RT-PCR for detecting viable Cochlodinium polykrikoides (Dinophyceae) cysts in sediment
inferred← citeshttps://doi.org/10.1016/j.hal.2017.04.002openalex-snapshot
Different life cycle strategies of the dinoflagellates Fragilidium duplocampanaeforme and its prey Dinophysis acuminata may explain their different susceptibilities to the infection by the parasite Parvilucifera infectans
inferred← citeshttps://doi.org/10.1016/j.hal.2017.07.008openalex-snapshot
The life history of the toxic marine dinoflagellate Protoceratium reticulatum (Gonyaulacales) in culture
inferred← citeshttps://doi.org/10.1016/j.hal.2017.12.001openalex-snapshot
Effects of modified clay used for the control of harmful algal blooms on Alexandrium pacificum cysts
inferred← citeshttps://doi.org/10.1016/j.hal.2018.01.006openalex-snapshot
Life histories of microalgal species causing harmful blooms: Haploids, diploids and the relevance of benthic stages
inferred← citeshttps://doi.org/10.1016/j.hal.2020.101788openalex-snapshot
Evidence for resting cyst production in the cosmopolitan toxic dinoflagellate Karlodinium veneficum and the cyst distribution in the China seas
inferred← citeshttps://doi.org/10.1016/j.hal.2020.101793openalex-snapshot
Morphology and molecular phylogeny of a new PST-producing dinoflagellate species: Alexandrium fragae sp. nov. (Gonyaulacales, dinophyceae)
inferred← citeshttps://doi.org/10.1016/j.hal.2020.101832openalex-snapshot
Alexandrium catenella cyst accumulation by passive and active dispersal agents: Implications for the potential spreading risk in Chilean Patagonian fjords
inferred← citeshttps://doi.org/10.1016/j.hal.2020.101921openalex-snapshot
Monoculture-based consumer-resource models predict species dominance in mixed batch cultures of dinoflagellates
inferred← citeshttps://doi.org/10.1016/j.hal.2021.102031openalex-snapshot
Transcriptomic and isotopic data reveal central role of ammonium in facilitating the growth of the mixotrophic dinoflagellate, Dinophysis acuminata
inferred← citeshttps://doi.org/10.1016/j.hal.2021.102050openalex-snapshot
Exploration of resting cysts (stages) and their relevance for possibly HABs-causing species in China
inferred← citeshttps://doi.org/10.1016/j.hal.2021.102064openalex-snapshot
Understanding controls on Margalefidinium polykrikoides blooms in the lower Chesapeake Bay
inferred← citeshttps://doi.org/10.1016/j.hal.2021.102079openalex-snapshot
Omics study of harmful algal blooms in China: Current status, challenges, and future perspectives
inferred← citeshttps://doi.org/10.1016/j.hal.2021.102121openalex-snapshot
Geographic distribution and historical presence of the resting cysts of Karenia mikimotoi in the seas of China
inferred← citeshttps://doi.org/10.1016/j.hal.2021.102130openalex-snapshot
Temperature-dependent growth and sexuality of the ciguatoxin producer dinoflagellate Gambierdiscus spp. in cultures established from the Canary Islands
inferred← citeshttps://doi.org/10.1016/j.hal.2022.102248openalex-snapshot
Energy metabolism and genetic information processing mark major transitions in the life history of Scrippsiella acuminata (Dinophyceae)
inferred← citeshttps://doi.org/10.1016/j.hal.2022.102307openalex-snapshot
Active meiosis during dinoflagellate blooms: A ‘sex for proliferation’ hypothesis
inferred← citeshttps://doi.org/10.1016/j.hal.2022.102312openalex-snapshot
Deficiency of nitrogen but not phosphorus triggers the life cycle transition of the dinoflagellate Scrippsiella acuminata from vegetative growth to resting cyst formation
inferred← citeshttps://doi.org/10.1016/j.hal.2022.102338openalex-snapshot
Six marine thecate Heterocapsa (Dinophyceae) from Malaysia, including the description of three novel species and their cytotoxicity potential
inferred← citeshttps://doi.org/10.1016/j.hal.2023.102427openalex-snapshot
The niche of a stress-tolerant specialist, Dinophysis acuminata, in a coastal upwelling system
inferred← citeshttps://doi.org/10.1016/j.hal.2023.102495openalex-snapshot
Small and patchy is enough: An example about how toxic HAB events can spread through low resting cyst loads
inferred← citeshttps://doi.org/10.1016/j.hal.2024.102658openalex-snapshot
Evidence for the production of asexual resting cysts in a free-living species of Symbiodiniaceae (Dinophyceae)
inferred← citeshttps://doi.org/10.1016/j.hal.2024.102746openalex-snapshot
Species and genetic diversity of notorious dinoflagellates Pfiesteria piscicida, Luciella masanensis, and relatives in marine sediments of China
inferred← citeshttps://doi.org/10.1016/j.hal.2025.102941openalex-snapshot
Single-cyst morpho-molecular identification detected an unexpected high species diversity of dinoflagellate resting cysts from the coastal seas of China
inferred← citeshttps://doi.org/10.1016/j.hal.2025.103002openalex-snapshot
A newly developed Germlings Harvester (GEHA) in combination with metabarcoding analysis detected numerous plankton species, particularly HABs-causing species, from in-situ germination of resting stage cells
inferred← citeshttps://doi.org/10.1016/j.hal.2025.103030openalex-snapshot
Melatonin promotes dinoflagellate cyst germination by crosstalk with abscisic acid and gibberellin
inferred← citeshttps://doi.org/10.1016/j.hal.2026.103064openalex-snapshot
Upwelling-driven vertical segregation of co-occurring phytoplankton, including HAB species, revealed by niche analyses
inferred← citeshttps://doi.org/10.1016/j.hal.2026.103083openalex-snapshot
Geographic and seasonal comparison of LSU rDNA copy numbers in Alexandrium catenella life cycle stages
inferred← citeshttps://doi.org/10.1016/j.hal.2026.103210openalex-snapshot
Multi-level evidence reveals a possibly vital role of H+-pyrophosphatase in the energetic metabolism of dinoflagellate resting cysts
inferred← citeshttps://doi.org/10.1016/j.heliyon.2024.e26495openalex-snapshot
Wide ecological niches ensure frequent harmful dinoflagellate blooms
inferred← citeshttps://doi.org/10.1016/j.ibiod.2019.02.006openalex-snapshot
Distribution of harmful dinoflagellate cysts in the surface sediments of Daya Bay of the South China Sea and their relationship to environmental factors
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2023.125116openalex-snapshot
Dinoflagellates as sustainable cellulose source: Cultivation, extraction, and characterization
inferred← citeshttps://doi.org/10.1016/j.jclepro.2026.148947openalex-snapshot
Ecological implications of fishery-photovoltaic systems: Altered phytoplankton dynamics and reduced microbial network stability under photovoltaic coverage
inferred← citeshttps://doi.org/10.1016/j.jmarsys.2015.01.006openalex-snapshot
Analysis of the hydrographic conditions and cyst beds in the San Jorge Gulf, Argentina, that favor dinoflagellate population development including toxigenic species and their toxins
inferred← citeshttps://doi.org/10.1016/j.jsames.2024.104878openalex-snapshot
Climatic variation of the last 29.000 years BP in the northern Santos basin (Rio de Janeiro Shelf) inferred by an alternation of cysts Tuberculodinium vancampoae and Operculodinium centrocarpum
inferred← citeshttps://doi.org/10.1016/j.jsames.2025.105783openalex-snapshot
Early Holocene climate transitions, fossil dinoflagellate cyst assemblages in the southern Gulf of California: Insights from the DIPAL IV core
inferred← citeshttps://doi.org/10.1016/j.marenvres.2023.106251openalex-snapshot
Plankton assemblages from microplastics of tropical coastal environments reveal high diversity and evidence of toxic species
inferred← citeshttps://doi.org/10.1016/j.marenvres.2024.106577openalex-snapshot
Transport and preservation of calcareous and organic-walled dinoflagellate cysts off Cape Blanc (NW africa) in relation to nepheloid layers
inferred← citeshttps://doi.org/10.1016/j.marenvres.2025.107768openalex-snapshot
The sterol composition of harmful dinoflagellates distinguishes environmental characteristics of Chilean Patagonia
inferred← citeshttps://doi.org/10.1016/j.marenvres.2026.107954openalex-snapshot
Dinoflagellate cysts revealed by combining microscopy and metabarcoding in the Taiwan Strait in Southeast China: the potential risk of harmful algal blooms
inferred← citeshttps://doi.org/10.1016/j.marmicro.2016.01.003openalex-snapshot
Dinoflagellate cyst distribution in the oligotrophic environments of the Gulf of Aqaba and northern Red Sea
inferred← citeshttps://doi.org/10.1016/j.marmicro.2019.03.013openalex-snapshot
Survival and recovery of the foraminifer Amphistegina gibbosa and associated diatom endosymbionts following up to 20 months in aphotic conditions
inferred← citeshttps://doi.org/10.1016/j.marmicro.2019.101816openalex-snapshot
Identifying the signature of sea-surface properties in dinocyst assemblages: Implications for quantitative palaeoceanographical reconstructions by transfer functions and analogue techniques
inferred← citeshttps://doi.org/10.1016/j.marmicro.2020.101824openalex-snapshot
A historical perspective on the development of the Northern Hemisphere modern dinoflagellate cyst database
inferred← citeshttps://doi.org/10.1016/j.marmicro.2020.101852openalex-snapshot
Distribution of dinoflagellate cysts along the salinity gradient in two tropical estuaries along the West coast of India
inferred← citeshttps://doi.org/10.1016/j.marmicro.2021.102000openalex-snapshot
Distribution of organic-walled dinoflagellate cysts in surface sediments of the southern Caribbean and the eastern tropical Pacific and its environmental implications
inferred← citeshttps://doi.org/10.1016/j.marmicro.2025.102449openalex-snapshot
Dinoflagellate cyst assemblages in recent sediments of Iran's tropical mangrove forests
inferred← citeshttps://doi.org/10.1016/j.marmicro.2025.102502openalex-snapshot
Progress, challenges and future directions in marine organic-walled dinoflagellate cyst research: New insights from an international workshop
inferred← citeshttps://doi.org/10.1016/j.marmicro.2026.102575openalex-snapshot
Complementarity of ancient DNA and microfossil records in a marine sedimentary archive from the Arctic
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2018.06.013openalex-snapshot
Molecular methods for cost-efficient monitoring of HAB (harmful algal bloom) dinoflagellate resting cysts
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2019.110825openalex-snapshot
Two - stages bloom of Margalefidinium cf. polykrikoides in a Mediterranean shallow bay (Ionian Sea, Italy)
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2021.112269openalex-snapshot
Dinoflagellate cyst distribution in surface sediments of Ambon Bay (eastern Indonesia): Environmental conditions and harmful blooms
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2022.114103openalex-snapshot
Continental shelf off northern Chilean Patagonia: A potential risk zone for the onset of Alexandrium catenella toxic bloom?
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2022.114567openalex-snapshot
A combined approach detected novel species diversity and distribution of dinoflagellate cysts in the Yellow Sea, China
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2024.116612openalex-snapshot
Environmental factors influencing the abundance and spatial distribution of modern dinoflagellate cysts in Izmir Bay (Eastern Mediterranean)
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2024.116832openalex-snapshot
Metabarcoding and co-occurrence network reveal significant effects of mariculture on benthic eukaryotic microalgal community: A case study in Daya Bay of the South China Sea
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2024.117059openalex-snapshot
Spatiotemporal dynamics of dinoflagellate communities in the Taiwan Strait and their correlations with micro-eukaryotic and bacterial communities
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2024.117080openalex-snapshot
Screening of ApDOT1.9 interacting proteins and the potential function of interactor ApSNARE in the rapid growth regulation of Alexandrium pacificum
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2024.117319openalex-snapshot
Assessment of dinoflagellate diversity using DNA metabarcoding reveals toxic dinoflagellate species in Australian coastal waters
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2025.117671openalex-snapshot
Physiological responses and sexual compatibility within a massive toxic bloom of Alexandrium minutum
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2025.117899openalex-snapshot
High-resolution DNA metabarcoding of modern surface sediments uncovers a diverse assemblage of dinoflagellate cysts in the Pacific and Arctic Oceans
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2025.118631openalex-snapshot
Controls on spatial heterogeneity in dinoflagellate cyst distribution in recent sediments off West Antarctica
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2025.119064openalex-snapshot
Shifts of dinoflagellate cyst assemblages over the past 100 years indicate the history of harmful algal blooms, eutrophication, and possible alien genotype invasion around the Shandong Peninsula, China
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2026.119568openalex-snapshot
An integrated morpho-molecular approach revealed dinoflagellate cysts diversity in ballast tank sediments of foreign ships
inferred← citeshttps://doi.org/10.1016/j.mitoco.2024.07.002openalex-snapshot
The mitochondria chronicles of melatonin and ATP: Guardians of phase separation
inferred← citeshttps://doi.org/10.1016/j.oceano.2021.09.002openalex-snapshot
Inhibitory effects of the brown macroalga Turbinaria ornata on cyst germination and progeny cells of five harmful dinoflagellate species
inferred← citeshttps://doi.org/10.1016/j.palaeo.2020.110055openalex-snapshot
Dinoflagellate cysts and ENSO-PDO climate forcing in the southern Gulf of California
inferred← citeshttps://doi.org/10.1016/j.pocean.2023.102999openalex-snapshot
When phytoplankton do not bloom: the case of the dinoflagellate Lepidodinium chlorophorum in southern Brittany (France) assessed by environmental DNA
inferred← citeshttps://doi.org/10.1016/j.pocean.2023.103000openalex-snapshot
Distribution of dinoflagellate cyst assemblages in surface sediments of Magellan fjords and channels (Patagonia, Chile) with a focus on harmful species: An overview on environmental scenario
inferred← citeshttps://doi.org/10.1016/j.protis.2015.01.001openalex-snapshot
Nuclear and Cell Morphological Changes during the Cell Cycle and Growth of the Toxic Dinoflagellate Alexandrium minutum
inferred← citeshttps://doi.org/10.1016/j.protis.2019.06.003openalex-snapshot
A Transcriptome-based Perspective of Meiosis in Dinoflagellates
inferred← citeshttps://doi.org/10.1016/j.quascirev.2023.108229openalex-snapshot
Dinocyst assemblages and water surface conditions in the Sea of Marmara during MIS 6 and 5 from two long cores
inferred← citeshttps://doi.org/10.1016/j.revmic.2018.09.003openalex-snapshot
Dinoflagellate fossils: Geological and biological applications
inferred← citeshttps://doi.org/10.1016/j.revpalbo.2024.105128openalex-snapshot
The utility of freshwater dinoflagellate cyst assemblages as a paleoecological proxy: An assessment from boreal lakes (northwest Ontario, Canada)
inferred← citeshttps://doi.org/10.1016/j.rsma.2020.101472openalex-snapshot
Dinoflagellate cyst assemblages as indicators of environmental conditions and shipping activities in coastal areas of the Black and Caspian Seas
inferred← citeshttps://doi.org/10.1016/j.rsma.2022.102502openalex-snapshot
Distribution of dinoflagellate cysts in the modern sediments from the coastal aquaculture area and its adjacent oceanic shelf in southeast China
inferred← citeshttps://doi.org/10.1016/j.rsma.2025.104284openalex-snapshot
Harmful algal blooms contribute to the dynamics of salt marsh ponds in a bar‐built estuary
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2017.11.269openalex-snapshot
Environmental forcing on the flux of organic-walled dinoflagellate cysts in recent sediments from a subtropical lagoon in the Gulf of California
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.147378openalex-snapshot
Drivers of dinoflagellate benthic cyst assemblages in the NW Patagonian Fjords System and its adjacent oceanic shelf, with a focus on harmful species
inferred← citeshttps://doi.org/10.1017/pab.2021.15openalex-snapshot
Size and shape variation in the calcareous nannoplankton genus Braarudosphaera following the Cretaceous/Paleogene (K/Pg) mass extinction: clues as to its evolutionary success
inferred← citeshttps://doi.org/10.1017/pab.2022.12openalex-snapshot
Morphometric analysis of Skiagia -plexus acritarchs from the early Cambrian of North Greenland: toward a meaningful evaluation of phenotypic plasticity
inferred← citeshttps://doi.org/10.1038/s41467-023-40657-4openalex-snapshot
Extreme environments offer an unprecedented opportunity to understand microbial eukaryotic ecology, evolution, and genome biology
inferred← citeshttps://doi.org/10.1038/s41564-020-00814-7openalex-snapshot
Dinoflagellates alter their carbon and nutrient metabolic strategies across environmental gradients in the central Pacific Ocean
inferred← citeshttps://doi.org/10.1038/s41597-025-04699-1openalex-snapshot
Full-length transcriptome analysis of a bloom-forming dinoflagellate Scrippsiella acuminata (Dinophyceae)
inferred← citeshttps://doi.org/10.1038/s41598-020-75194-3openalex-snapshot
Stressor-induced ecdysis and thecate cyst formation in the armoured dinoflagellates Prorocentrum cordatum
inferred← citeshttps://doi.org/10.1038/s41598-021-04227-2openalex-snapshot
Cryoprotectant treatment tests on three morphologically diverse marine dinoflagellates and the cryopreservation of Breviolum sp. (Symbiodiniaceae)
inferred← citeshttps://doi.org/10.1038/s41598-021-98148-9openalex-snapshot
Direct evidence of sex and a hypothesis about meiosis in Symbiodiniaceae
inferred← citeshttps://doi.org/10.1038/s41598-023-41339-3openalex-snapshot
Phosphorus deficiency induces sexual reproduction in the dinoflagellate Prorocentrum cordatum
inferred← citeshttps://doi.org/10.1038/s41598-026-65036-zopenalex-snapshot
Winter sediment resuspension in a submarine canyon drives the offshore export of toxigenic Alexandrium catenella cysts
inferred← citeshttps://doi.org/10.1038/srep45850openalex-snapshot
Eukaryotic Life Inhabits Rhodolith-forming Coralline Algae (Hapalidiales, Rhodophyta), Remarkable Marine Benthic Microhabitats
inferred← citeshttps://doi.org/10.1080/00288330.2015.1110187openalex-snapshot
Historical deposits of Alexandrium catenella resting cysts in the sediments of Queen Charlotte Sound, New Zealand
inferred← citeshttps://doi.org/10.1080/00318884.2019.1620582openalex-snapshot
Morphology, phylogeny and life cycle of Fragilidium mexicanum Balech (Gonyaulacales, Dinophyceae)
inferred← citeshttps://doi.org/10.1080/01916122.2014.990115openalex-snapshot
A determination key for modern dinoflagellate cysts
inferred← citeshttps://doi.org/10.1080/01916122.2016.1276027openalex-snapshot
The influence of dissolved oxygen on dinoflagellate cyst distribution across Sluice Pond, a meromictic lake in NE Massachusetts, USA
inferred← citeshttps://doi.org/10.1080/01916122.2023.2273267openalex-snapshot
Dinoflagellate cyst distribution over the past 9 kyrs BP from offshore east Tasmania, southeast Australia
inferred← citeshttps://doi.org/10.1080/09670262.2014.915062openalex-snapshot
Development, morphological characteristics and viability of temporary cysts ofPyrodinium bahamensevar.compressum(Dinophyceae)in vitro
inferred← citeshttps://doi.org/10.1080/09670262.2018.1455111openalex-snapshot
Species diversity and abundance of dinoflagellate resting cysts seven months after a bloom of Alexandrium catenella in two contrasting coastal systems of the Chilean Inland Sea
inferred← citeshttps://doi.org/10.1080/09670262.2018.1563216openalex-snapshot
Cell death in individual freshwater phytoplankton species: relationships with population dynamics and environmental factors
inferred← citeshttps://doi.org/10.1080/09670262.2021.1885066openalex-snapshot
Export flux succession of dinoflagellate cysts and planktonic foraminifera in an active upwelling cell off Cape Blanc (NW Africa)
inferred← citeshttps://doi.org/10.1080/09670262.2025.2450678openalex-snapshot
Linking new DNA sequence data to old scientific names of Parvodinium (Peridiniopsidaceae, Dinophyceae)
inferred← citeshttps://doi.org/10.1080/14634988.2017.1403269openalex-snapshot
Harmful non-indigenous dinoflagellate cysts in China: A review
inferred← citeshttps://doi.org/10.1093/biosci/biab101openalex-snapshot
Eutrophication on Coral Reefs: What Is the Evidence for Phase Shifts, Nutrient Limitation and Coral Bleaching
inferred← citeshttps://doi.org/10.1093/molbev/msw119openalex-snapshot
Sex, Scavengers, and Chaperones: Transcriptome Secrets of DivergentSymbiodiniumThermal Tolerances
inferred← citeshttps://doi.org/10.1093/plankt/fby020openalex-snapshot
Seed bank and seasonal patterns of the eukaryotic SAR (Stramenopila, Alveolata and Rhizaria) clade in a New England vernal pool
inferred← citeshttps://doi.org/10.1093/plphys/kiag524openalex-snapshot
Light-dependent processes in algae across scales: from cellular physiology to ecological organization
inferred← citeshttps://doi.org/10.1099/mic.0.000653openalex-snapshot
Encystation: the most prevalent and underinvestigated differentiation pathway of eukaryotes
inferred← citeshttps://doi.org/10.1111/1462-2920.15863openalex-snapshot
Protistan plankton communities in the Galápagos Archipelago respond to changes in deep water masses resulting from the 2015/16 El Niño
inferred← citeshttps://doi.org/10.1111/1755-0998.13903openalex-snapshot
Evaluating the use of lake sedimentary DNA in palaeolimnology: A comparison with long‐term microscopy‐based monitoring of the phytoplankton community
inferred← citeshttps://doi.org/10.1111/aec.12852openalex-snapshot
A functional deconstructive approach to mixotrophic phytoplankton responds better to local, regional and biogeographic predictors than species
inferred← citeshttps://doi.org/10.1111/are.13815openalex-snapshot
Towards control of unwanted cyst-forming dinoflagellates in aquaculture systems: Knockout and recovery of Pfiesteria sp. after peracetic acid exposure
inferred← citeshttps://doi.org/10.1111/fwb.70260openalex-snapshot
Ecological Dynamics and Characteristics of Mountain Lakes: Insights Into Diversity and Understanding Phytoplankton Resilience
inferred← citeshttps://doi.org/10.1111/jeu.12231openalex-snapshot
Euduboscquella costata n. sp. (Dinoflagellata, Syndinea), an Intracellular Parasite of the Ciliate Schmidingerella arcuata : Morphology, Molecular Phylogeny, Life Cycle, Prevalence, and Infection Intensity
inferred← citeshttps://doi.org/10.1111/jeu.12681openalex-snapshot
Cloning and Partial Characterization of a Cold Shock Domain‐Containing Protein Gene from the Dinoflagellate Scrippsiella trochoidea
inferred← citeshttps://doi.org/10.1111/jeu.12827openalex-snapshot
Microeukaryotic Communities Associated With the Seagrass Zostera marina Are Spatially Structured
inferred← citeshttps://doi.org/10.1111/jeu.13005openalex-snapshot
Single‐cell DNA from West Greenland marine sediments suggests presence of Protoperidinium tricingulatum in the Arctic
inferred← citeshttps://doi.org/10.1111/jeu.13015openalex-snapshot
The second most abundant dinophyte in the ponds of a botanical garden is a species new to science
inferred← citeshttps://doi.org/10.1111/jpy.12257openalex-snapshot
First report of fossilized cysts produced by the benthic B ysmatrum subsalsum ( D inophyceae) from a shallow M exican lagoon in the G ulf of M exico
inferred← citeshttps://doi.org/10.1111/jpy.12274openalex-snapshot
Sexual resting cyst production by the dinoflagellate Akashiwo sanguinea : a potential mechanism contributing to the ubiquitous distribution of a harmful alga
inferred← citeshttps://doi.org/10.1111/jpy.12337openalex-snapshot
Life history, excystment features, and growth characteristics of the Mediterranean harmful dinoflagellate Alexandrium pseudogonyaulax
inferred← citeshttps://doi.org/10.1111/jpy.12485openalex-snapshot
Discovery of a resting stage in the harmful, brown‐tide‐causing pelagophyte, Aureoumbra lagunensis: a mechanism potentially facilitating recurrent blooms and geographic expansion
inferred← citeshttps://doi.org/10.1111/jpy.12611openalex-snapshot
Benthic flattened cells of the phylogenetically related marine dinoflagellates Protoceratium reticulatum and Ceratocorys mariaovidiorum (Gonyaulacales): a new type of cyst?
inferred← citeshttps://doi.org/10.1111/jpy.12756openalex-snapshot
The potential for dispersal of microalgal resting cysts by migratory birds
inferred← citeshttps://doi.org/10.1111/jpy.12783openalex-snapshot
Laciniporus arabicusgen. et sp. nov. (Dinophyceae, Peridiniales), a new thecate, marine, sand‐dwelling dinoflagellate from the northern Indian Ocean (Arabian Sea)1
inferred← citeshttps://doi.org/10.1111/jpy.12919openalex-snapshot
Generalist Life Cycle Aids Persistence of Alexandrium ostenfeldii (Dinophyceae) in Seasonal Coastal Habitats of the Baltic Sea
inferred← citeshttps://doi.org/10.1111/jpy.12925openalex-snapshot
Evidence for Production of Sexual Resting Cysts by the Toxic Dinoflagellate Karenia mikimotoi in Clonal Cultures and Marine Sediments
inferred← citeshttps://doi.org/10.1111/jpy.12989openalex-snapshot
Life Cycle Stages and Evidence of Sexual Reproduction in the Marine DinoflagellateProrocentrum minimum(Dinophyceae, Prorocentrales)
inferred← citeshttps://doi.org/10.1111/jpy.13382openalex-snapshot
Does dinocyst wall composition really reflect trophic affinity? New evidence from ATR micro‐FTIR spectroscopy measurements
inferred← citeshttps://doi.org/10.1111/jpy.70151openalex-snapshot
Phytoplankton community structure in a subtropical river revealed by DNA metabarcoding, with a focus on cell‐cyst coupling of Unruhdinium spp. (Dinophyceae)
inferred← citeshttps://doi.org/10.1111/jpy.70201openalex-snapshot
Revisiting the life cycle of Margalefidinium polykrikoides Group III
inferred← citeshttps://doi.org/10.1111/pala.12722openalex-snapshot
The palaeobiological significance of clustering in acritarchs: a case study from the early Cambrian of North Greenland
inferred← citeshttps://doi.org/10.1126/sciadv.adk1033openalex-snapshot
Climate change, society, and pandemic disease in Roman Italy between 200 BCE and 600 CE
inferred← citeshttps://doi.org/10.1126/sciadv.ads7789openalex-snapshot
Broad active metabolic pathways, autophagy, and antagonistic hormones regulate dinoflagellate cyst dormancy in marine sediments
inferred← citeshttps://doi.org/10.1127/pip/2016/0039openalex-snapshot
Unravelling the functional genetics of dinoflagellates: a review of approaches and opportunities
inferred← citeshttps://doi.org/10.1128/msphere.00366-24openalex-snapshot
Interaction patterns and assembly mechanisms of dinoflagellates and diatoms in a coastal bay suffering from long-term eutrophication
inferred← citeshttps://doi.org/10.1144/sp511-2020-109openalex-snapshot
Non-pollen palynomorphs in freshwater sediments and their palaeolimnological potential and selected applications
inferred← citeshttps://doi.org/10.1144/sp511-2020-55openalex-snapshot
Marine dinocysts, acritarchs and less well-known NPP: tintinnids, ostracod and foraminiferal linings, copepod and worm remains
inferred← citeshttps://doi.org/10.1146/annurev-marine-042021-012353openalex-snapshot
Temporal and Spatial Signaling Mediating the Balance of the Plankton Microbiome
inferred← citeshttps://doi.org/10.1186/s12864-021-07840-7openalex-snapshot
Transcriptome and metabolome analyses of cold and darkness-induced pellicle cysts of Scrippsiella trochoidea
inferred← citeshttps://doi.org/10.1186/s12864-024-10847-5openalex-snapshot
A decade of dinoflagellate genomics illuminating an enigmatic eukaryote cell
inferred← citeshttps://doi.org/10.1186/s12915-021-00994-6openalex-snapshot
Comparison of 15 dinoflagellate genomes reveals extensive sequence and structural divergence in family Symbiodiniaceae and genus Symbiodinium
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