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Toxigenic strains of Azadinium poporum (Amphidomataceae, Dinophyceae) from Japan and Vietnam, with first reports of A. poporum (ribotype A) and A. trinitatum in Asian Pacific
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1522-7189(199905/06)7:3<99::aid-nt46>3.0.co;2-lopenalex-snapshot
Two analogs of azaspiracid isolated from mussels, Mytilus edulis, involved in human intoxication in Ireland
inferredcites →https://doi.org/10.1007/978-3-319-70069-4_14openalex-snapshot
Overview of Harmful Algal Blooms in Asia
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Mediterranean Azadinium dexteroporum (Dinophyceae) produces six novel azaspiracids and azaspiracid-35: a structural study by a multi-platform mass spectrometry approach
inferredcites →https://doi.org/10.1007/s10811-015-0667-5openalex-snapshot
Detection of Azadinium poporum in New Zealand: the use of molecular tools to assist with species isolations
inferredcites →https://doi.org/10.1007/s13199-012-0195-xopenalex-snapshot
Multiple microalgal partners in symbiosis with the acantharian Acanthochiasma sp. (Radiolaria)
inferredcites →https://doi.org/10.1016/j.ecoenv.2016.01.017openalex-snapshot
Growth and toxin production of Azadinium poporum strains in batch cultures under different nutrient conditions
inferredcites →https://doi.org/10.1016/j.hal.2007.12.003openalex-snapshot
Phylogenetic relationships in the harmful dinoflagellate Cochlodinium polykrikoides (Gymnodiniales, Dinophyceae) inferred from LSU rDNA sequences
inferredcites →https://doi.org/10.1016/j.hal.2012.10.001openalex-snapshot
First record of the genus Azadinium (Dinophyceae) from the Shetland Islands, including the description of Azadinium polongum sp. nov.
inferredcites →https://doi.org/10.1016/j.hal.2012.11.009openalex-snapshot
Morphology, phylogeny and azaspiracid profile of Azadinium poporum (Dinophyceae) from the China Sea
inferredcites →https://doi.org/10.1016/j.hal.2013.05.009openalex-snapshot
Effect of environmental and nutritional factors on growth and azaspiracid production of the dinoflagellate Azadinium spinosum
inferredcites →https://doi.org/10.1016/j.hal.2014.04.012openalex-snapshot
Azaspiracid variability of Azadinium poporum (Dinophyceae) from the China Sea
inferredcites →https://doi.org/10.1016/j.hal.2015.11.001openalex-snapshot
Azadinium poporum from the Argentine Continental Shelf, Southwestern Atlantic, produces azaspiracid-2 and azaspiracid-2 phosphate
inferredcites →https://doi.org/10.1016/j.hal.2016.02.006openalex-snapshot
Morphology, molecular phylogeny and azaspiracid profile of Azadinium poporum (Dinophyceae) from the Gulf of Mexico
inferredcites →https://doi.org/10.1016/j.hal.2016.12.001openalex-snapshot
Amphidoma languida (Amphidomatacea, Dinophyceae) with a novel azaspiracid toxin profile identified as the cause of molluscan contamination at the Atlantic coast of southern Spain
inferredcites →https://doi.org/10.1016/j.hal.2017.05.001openalex-snapshot
Adding new pieces to the Azadinium (Dinophyceae) diversity and biogeography puzzle: Non-toxigenic Azadinium zhuanum sp. nov. from China, toxigenic A. poporum from the Mediterranean, and a non-toxigenic A. dalianense from the French Atlantic
inferredcites →https://doi.org/10.1016/j.hal.2017.08.004openalex-snapshot
Identification of Azadinium species and a new azaspiracid from Azadinium poporum in Puget Sound, Washington State, USA
inferredcites →https://doi.org/10.1016/j.hal.2018.08.003openalex-snapshot
Sympatric occurrence of two Azadinium poporum ribotypes in the Eastern Mediterranean Sea
inferredcites →https://doi.org/10.1016/j.hal.2018.08.011openalex-snapshot
Diversity, distribution, and azaspiracids of Amphidomataceae (Dinophyceae) along the Norwegian coast
inferredcites →https://doi.org/10.1016/j.hal.2019.101637openalex-snapshot
Occurrence and distribution of Amphidomataceae (Dinophyceae) in Danish coastal waters of the North Sea, the Limfjord and the Kattegat/Belt area
inferredcites →https://doi.org/10.1016/j.hal.2020.101776openalex-snapshot
Over 30 years of HABs in the Philippines and Malaysia: What have we learned?
inferredcites →https://doi.org/10.1016/j.hal.2020.101787openalex-snapshot
Harmful algal blooms and associated fisheries damage in East Asia: Current status and trends in China, Japan, Korea and Russia
inferredcites →https://doi.org/10.1016/j.protis.2011.10.005openalex-snapshot
Amphidoma languida sp. nov. (Dinophyceae) Reveals a Close Relationship between Amphidoma and Azadinium
inferredcites →https://doi.org/10.1016/j.protis.2014.04.004openalex-snapshot
Morphological and Molecular Characterization of Three New Azadinium Species (Amphidomataceae, Dinophyceae) from the Irminger Sea
inferredcites →https://doi.org/10.1016/j.protis.2015.10.003openalex-snapshot
Two New Freshwater Woloszynskioids Asulcocephalium miricentonis gen. et sp. nov. and Leiocephalium pseudosanguineum gen. et sp. nov. (Suessiaceae, Dinophyceae) Lacking an Apical Furrow Apparatus
inferredcites →https://doi.org/10.1016/j.protis.2019.125680openalex-snapshot
Gertia stigmatica gen. et sp. nov. (Kareniaceae, Dinophyceae), a New Marine Unarmored Dinoflagellate Possessing the Peridinin-type Chloroplast with an Eyespot
inferredcites →https://doi.org/10.1016/j.toxicon.2009.02.008openalex-snapshot
Isolation of azaspiracid-2 from a marine sponge Echinoclathria sp. as a potent cytotoxin
inferredcites →https://doi.org/10.1016/j.toxicon.2009.10.020openalex-snapshot
First evidence of azaspiracids (AZAs): A family of lipophilic polyether marine toxins in scallops (Argopecten purpuratus) and mussels (Mytilus chilensis) collected in two regions of Chile
inferredcites →https://doi.org/10.1016/j.toxicon.2012.05.007openalex-snapshot
New azaspiracids in Amphidomataceae (Dinophyceae)
inferredcites →https://doi.org/10.1016/s0041-0101(02)00244-1openalex-snapshot
Ubiquitous ‘benign’ alga emerges as the cause of shellfish contamination responsible for the human toxic syndrome, azaspiracid poisoning
inferredcites →https://doi.org/10.1021/ja981413ropenalex-snapshot
Azaspiracid, a New Marine Toxin Having Unique Spiro Ring Assemblies, Isolated from Irish Mussels, Mytilus edulis
inferredcites →https://doi.org/10.1080/00318884.2019.1601948openalex-snapshot
Morphological variation, ultrastructure, pigment composition and phylogeny of the star-shaped dinoflagellateAsterodinium gracile(Kareniaceae, Dinophyceae)
inferredcites →https://doi.org/10.1080/00318884.2019.1658399openalex-snapshot
Dactylodinium arachnoides sp. nov . (Borghiellaceae, Dinophyceae): a new marine dinoflagellate with a loop-shaped apical structure complex and tubular membranous extrusomes
inferredcites →https://doi.org/10.1080/00318884.2019.1670013openalex-snapshot
Amphidomataceae (Dinophyceae) in the western Greenland area, including description of Azadinium perforatum sp. nov.
inferredcites →https://doi.org/10.1080/02652030400002105openalex-snapshot
Azaspiracid poisoning, the food-borne illness associated with shellfish consumption
inferredcites →https://doi.org/10.1080/09670260802578534openalex-snapshot
Azadinium spinosumgen. et sp. nov. (Dinophyceae) identified as a primary producer of azaspiracid toxins
inferredcites →https://doi.org/10.1080/09670262.2011.556753openalex-snapshot
A new non-toxic species in the dinoflagellate genusAzadinium:A. poporumsp. nov.
inferredcites →https://doi.org/10.1080/09670262.2017.1346205openalex-snapshot
Amphidoma parvula (Amphidomataceae), a new planktonic dinophyte from the Argentine Sea
inferredcites →https://doi.org/10.1080/17451000.2013.866252openalex-snapshot
Azadinium caudatumvar.margalefii, a poorly known member of the toxigenic genusAzadinium(Dinophyceae)
inferredcites →https://doi.org/10.1093/molbev/mst197openalex-snapshot
MEGA6: Molecular Evolutionary Genetics Analysis Version 6.0
inferredcites →https://doi.org/10.1093/nar/25.24.4876openalex-snapshot
The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools
inferredcites →https://doi.org/10.1093/plankt/fbw099openalex-snapshot
Identification ofAzadinium poporum(Dinophyceae) in the Southeast Pacific: morphology, molecular phylogeny, and azaspiracid profile characterization
inferredcites →https://doi.org/10.1111/j.0908-8857.2004.03297.xopenalex-snapshot
Glacial history and colonization of Europe by the blue tit Parus caeruleus
inferredcites →https://doi.org/10.1111/j.1440-1835.2007.00466.xopenalex-snapshot
Cochlodinium fulvescens sp. nov. (Gymnodiniales, Dinophyceae), a new chain‐forming unarmored dinoflagellate from Asian coasts
inferredcites →https://doi.org/10.1111/j.1529-8817.1987.tb04217.xopenalex-snapshot
MEDIA FOR THE CULTURE OF OCEANIC ULTRAPHYTOPLANKTON 1,2
inferredcites →https://doi.org/10.1111/j.1529-8817.2012.01159.xopenalex-snapshot
TAXONOMIC REVISION OF THE DINOFLAGELLATE AMPHIDOMA CAUDATA : TRANSFER TO THE GENUS AZADINIUM (DINOPHYCEAE) AND PROPOSAL OF TWO VARIETIES, BASED ON MORPHOLOGICAL AND MOLECULAR PHYLOGENETIC ANALYSES 1
inferredcites →https://doi.org/10.1111/j.1550-7408.2011.00600.xopenalex-snapshot
First Report of the Photosynthetic Dinoflagellate Genus A zadinium in the P acific O cean: Morphology and Molecular Characterization of A zadinium cf. poporum
inferredcites →https://doi.org/10.1111/jpy.12104openalex-snapshot
A new potentially toxic A zadinium species ( D inophyceae) from the M editerranean Sea, A . dexteroporum sp. nov.
inferredcites →https://doi.org/10.1111/jpy.12575openalex-snapshot
Dactylodinium pterobelotum gen. et sp. nov., a new marine woloszynskioid dinoflagellate positioned between the two families Borghiellaceae and Suessiaceae
inferredcites →https://doi.org/10.1111/pre.12133openalex-snapshot
Revisiting the 1991 algal bloom in shelf waters off Argentina: Azadinium luciferelloides sp. nov. (Amphidomataceae, Dinophyceae) as the causative species in a diverse community of other amphidomataceans
inferredcites →https://doi.org/10.1111/pre.12225openalex-snapshot
Electron microscopy of a 1991 spring plankton sample from the Argentinean Shelf reveals the presence of four new species of the Amphidomataceae (Dinophyceae)
inferredcites →https://doi.org/10.1111/pre.12448openalex-snapshot
Morphological and molecular characterization of multiple new Azadinium strains revealed a high diversity of non‐toxigenic species of Amphidomataceae (Dinophyceae ) including two new Azadinium species in Irish waters, North East Atlantic
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/10.1201/b16662-32openalex-snapshot
Ciguatera Toxins: Pharmacology, Toxicology, and Detection
inferredcites →https://doi.org/10.2216/13-178.1openalex-snapshot
Azadinium dalianense , a new dinoflagellate species from the Yellow Sea, China
inferredcites →https://doi.org/10.2216/13-192.1openalex-snapshot
Morphology of two marine woloszynskioid dinoflagellates, Biecheleria brevisulcata sp. nov. and Biecheleriopsis adriatica (Suessiaceae, Dinophyceae), from Japanese coasts
inferredcites →https://doi.org/10.2216/i0031-8884-39-4-302.1openalex-snapshot
Phylogeny of some of the major genera of dinoflagellates based on ultrastructure and partial LSU rDNA sequence data, including the erection of three new genera of unarmoured dinoflagellates
inferredcites →https://doi.org/10.2216/ph09-35.1openalex-snapshot
Azadinium obesum (Dinophyceae), a new nontoxic species in the genus that can produce azaspiracid toxins
inferredcites →https://doi.org/10.2983/035.034.0340openalex-snapshot
Diarrhetic Shellfish Toxins in Primorsky Krai, Russia
inferredcites →https://doi.org/10.2983/0730-8000(2006)25[1067:fdoaim]2.0.co;2openalex-snapshot
FIRST DETECTION OF AZASPIRACIDS IN MUSSELS IN NORTH WEST AFRICA
inferredcites →https://doi.org/10.3390/md17090489openalex-snapshot
Effects of Temperature, Growth Media, and Photoperiod on Growth and Toxin Production of Azadinium spinosum
inferredcites →https://doi.org/10.3724/sp.j.1123.2010.00363openalex-snapshot
Determination of azaspiracid-1 in shellfishes by liquid chromatography with tandem mass spectrometry
inferredcites →https://doi.org/10.3800/pbr.1.183openalex-snapshot
A new diplopsalid species Oblea acanthocysta sp. nov. (Peridiniales, Dinophyceae)
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2023.140109openalex-snapshot
Occurrence and phase distribution of lipophilic marine algal toxins in the bottom boundary layer and sediment-porewater system of two mariculture sites
inferred← citeshttps://doi.org/10.1016/j.ecss.2025.109416openalex-snapshot
Differential accumulation of dissolved azaspiracids and diarrhetic shellfish toxins in Manila clam (Ruditapes philippinarum): effects of temperature and tissue-specific uptake
inferred← citeshttps://doi.org/10.1016/j.ecss.2026.110320openalex-snapshot
Harmful marine dinoflagellates in Vietnam: A review of their distribution, toxin production, and environmental impact
inferred← citeshttps://doi.org/10.1016/j.ejop.2021.125811openalex-snapshot
Thecal tabulation, body scale morphology and phylogeny of Heterocapsa philippinensis sp. nov. (Peridiniales, Dinophyceae) from the Philippines
inferred← citeshttps://doi.org/10.1016/j.ejop.2026.126182openalex-snapshot
Azadinium fusiforme, a new species of Amphidomataceae from Korean and Japanese coastal waters that lacks azaspiracid production
inferred← citeshttps://doi.org/10.1016/j.ejop.2026.126205openalex-snapshot
Pentapharsodinium ocelliferum sp. nov. (Ensiculiferaceae, Dinophyceae), a novel armored dinoflagellate with an eyespot from the Philippines
inferred← citeshttps://doi.org/10.1016/j.hal.2021.102059openalex-snapshot
Emerging harmful algal bloom species over the last four decades in China
inferred← citeshttps://doi.org/10.1016/j.hal.2021.102063openalex-snapshot
Diversity and distribution of harmful microalgae in the Gulf of Thailand assessed by DNA metabarcoding
inferred← citeshttps://doi.org/10.1016/j.hal.2022.102204openalex-snapshot
Morphological variation and phylogeny of Karenia selliformis (Gymnodiniales, Dinophyceae) in an intensive cold-water algal bloom in eastern Hokkaido, Japan
inferred← citeshttps://doi.org/10.1016/j.hal.2023.102404openalex-snapshot
Metabarcoding revealed a high diversity of Amphidomataceae (Dinophyceae) and the seasonal distribution of their toxigenic species in the Taiwan Strait
inferred← citeshttps://doi.org/10.1016/j.hal.2024.102701openalex-snapshot
Phylogeny and ultrastructure of a non-toxigenic dinoflagellate Amphidoma fulgens sp. nov. (Amphidomataceae, Dinophyceae), with a wide distribution across Asian Pacific
inferred← citeshttps://doi.org/10.1016/j.hal.2025.102969openalex-snapshot
Diversity of amphidomatacean dinoflagellates in Japan, with a description of Azadinium inconspicuum sp. nov. and azaspiracid components in Azadinium poporum ribotypes
inferred← citeshttps://doi.org/10.1016/j.hal.2026.103103openalex-snapshot
Unlocking species and subspecies diversity of harmful microalgae using HiFi long-read metabarcoding: insights from Amphidomataceae (Dinophyceae) in the China Sea
inferred← citeshttps://doi.org/10.1016/j.hal.2026.103196openalex-snapshot
Intracellular ultrastructural characterization of Azadinium and Amphidoma (Amphidomataceae, Dinophyceae), including toxigenic and non-toxigenic strains
inferred← citeshttps://doi.org/10.1016/j.jchromb.2024.124065openalex-snapshot
New azaspiracid analogues detected as bi-charged ions in Azadinium poporum (Amphidomataceae, Dinophyceae) isolated from Japanese coastal waters
inferred← citeshttps://doi.org/10.1016/j.jchromb.2025.124826openalex-snapshot
Novel isotope-coded derivatization of carboxylic acids provides accurate quantification of Azaspiracids in shellfish by liquid chromatography–tandem mass spectrometry
inferred← citeshttps://doi.org/10.1016/j.toxicon.2021.06.010openalex-snapshot
Complex profiles of azaspiracid analogues in two culture strains of Azadinium poporum (Amphidomataceae, Dinophyceae) isolated from Japanese coastal waters determined by LC-MS/MS
inferred← citeshttps://doi.org/10.1016/j.toxicon.2023.107069openalex-snapshot
Azaspiracid accumulation in Japanese coastal bivalves and ascidians fed with Azadinium poporum producing azaspiracid-2 as the dominant toxin component
inferred← citeshttps://doi.org/10.1016/j.toxicon.2026.109148openalex-snapshot
Structure elucidation and in vitro toxicity of AZA-40, an azaspiracid isobaric to AZA-1
inferred← citeshttps://doi.org/10.1080/00318884.2023.2204681openalex-snapshot
A new small thecate dinoflagellate Azadinium anteroporum sp. nov . (Amphidomataceae, Dinophyceae) isolated from the Asian Pacific
inferred← citeshttps://doi.org/10.1093/plankt/fbag029openalex-snapshot
Molecular detections of 14 amphidomatacean species (Dinophyceae) and their temperature-associated distribution in subarctic waters off eastern Hokkaido, Japan
inferred← citeshttps://doi.org/10.1111/jeu.13082openalex-snapshot
Kapelodiniopsis flava n. g., n. sp. (Dinophyceae), a new katodinioid with haptophyte‐derived plastids of multiple origins: Implications for the plastid integration process
inferred← citeshttps://doi.org/10.1111/pre.12567openalex-snapshot
First report of toxigenic Amphidoma languida (Amphidomataceae, Dinophyceae) from the Pacific, with reference to intracellular ultrastructure and azaspiracid compounds
inferred← citeshttps://doi.org/10.1111/pre.70001openalex-snapshot
Diversity of Amphidomataceae (Dinophyceae) in the Black Sea, including description of Amphidoma pontica sp. nov.
inferred← citeshttps://doi.org/10.1371/journal.pone.0264143openalex-snapshot
Using RDNA sequences to define dinoflagellate species
inferred← citeshttps://doi.org/10.2331/suisan.wa2980-7openalex-snapshot
7. Study on azaspiracid shellfish poisoning in Japan
inferred← citeshttps://doi.org/10.3389/frpro.2025.1612811openalex-snapshot
Vertical distribution of harmful algae in the sediment of Uranouchi Inlet by metabarcoding
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