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A new non-toxic species in the dinoflagellate genusAzadinium:A. poporumsp. nov.

https://doi.org/10.1080/09670262.2011.556753
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What this work says

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

inferredcites →https://doi.org/10.1016/0269-7491(90)90174-bopenalex-snapshot
Novel phytoplankton blooms: Causes and impacts of recurrent brown tides and other unusual blooms
inferredcites →https://doi.org/10.1016/j.chroma.2003.10.045openalex-snapshot
Liquid chromatography—multiple tandem mass spectrometry for the determination of ten azaspiracids, including hydroxyl analogues in shellfish
inferredcites →https://doi.org/10.1016/j.hal.2007.05.002openalex-snapshot
Two decades of marine biotoxin monitoring in bivalves from Portugal (1986–2006): A review of exposure assessment
inferredcites →https://doi.org/10.1016/j.hal.2008.06.003openalex-snapshot
Characterization of azaspiracids in plankton size-fractions and isolation of an azaspiracid-producing dinoflagellate from the North Sea
inferredcites →https://doi.org/10.1016/j.toxicon.2009.07.014openalex-snapshot
First identification of azaspiracid and spirolides in Mesodesma donacium and Mulinia edulis from Northern Chile
inferredcites →https://doi.org/10.1016/s0003-9365(85)80012-9openalex-snapshot
An SEM study of Amphidoma nucula (dinophyceae) and description of the thecal plates in A. caudata
inferredcites →https://doi.org/10.1016/s0041-0101(02)00082-xopenalex-snapshot
First evidence of an extensive northern European distribution of azaspiracid poisoning (AZP) toxins in shellfish
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/10.1016/s0041-0101(02)00288-xopenalex-snapshot
Detection of five new hydroxyl analogues of azaspiracids in shellfish using multiple tandem mass spectrometry
inferredcites →https://doi.org/10.1016/s0041-0101(03)00105-3openalex-snapshot
The first identification of azaspiracids in shellfish from France and Spain
inferredcites →https://doi.org/10.1029/ce035p0383openalex-snapshot
The Chrysochromulina polylepis bloom in Scandinavian waters during spring 1988
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/10.1080/10635150390235520openalex-snapshot
A Simple, Fast, and Accurate Algorithm to Estimate Large Phylogenies by Maximum Likelihood
inferredcites →https://doi.org/10.1080/10635150490522304openalex-snapshot
Model Selection and Model Averaging in Phylogenetics: Advantages of Akaike Information Criterion and Bayesian Approaches Over Likelihood Ratio Tests
inferredcites →https://doi.org/10.1093/bioinformatics/14.9.817openalex-snapshot
MODELTEST: testing the model of DNA substitution.
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/oxfordjournals.molbev.a003851openalex-snapshot
A General Empirical Model of Protein Evolution Derived from Multiple Protein Families Using a Maximum-Likelihood Approach
inferredcites →https://doi.org/10.1111/j.0022-3646.1985.00662.xopenalex-snapshot
A RAPID SIMPLE TECHNIQUE UTILIZING CALCOFLUOR WHITE M2R FOR THE VISUALIZATION OF DINOFLAGELLATE THECAL PLATES 1
inferredcites →https://doi.org/10.1111/j.1095-8339.1971.tb02138.xopenalex-snapshot
A fine-structural survey of dinoflagellate pyrenoids and food-reserves
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.1529-8817.2004.03060.xopenalex-snapshot
ALEXANDRIUM TAMUTUM SP. NOV. (DINOPHYCEAE): A NEW NONTOXIC SPECIES IN THE GENUS ALEXANDRIUM1
inferredcites →https://doi.org/10.1111/j.1529-8817.2005.04168.xopenalex-snapshot
PHYLOGENY OF DINOFLAGELLATES BASED ON MITOCHONDRIAL CYTOCHROME B AND NUCLEAR SMALL SUBUNIT RDNA SEQUENCE COMPARISONS1
inferredcites →https://doi.org/10.1111/j.1558-5646.1985.tb00420.xopenalex-snapshot
CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP
inferredcites →https://doi.org/10.1242/jcs.1.2.187openalex-snapshot
Further observations on the fine structure of Chrysochromulina chiton, with special reference to the pyrenoid
inferredcites →https://doi.org/10.2216/i0031-8884-41-1-22.1openalex-snapshot
Diel changes in pyrenoid and starch reserves in 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/10.2983/0730-8000(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/md6020039openalex-snapshot
Azaspiracid Shellfish Poisoning: A Review on the Chemistry, Ecology, and Toxicology with an Emphasis on Human Health Impacts

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.4591756openalex-extracted
inferred← citeshttps://doi.org/10.1002/9781118994672.ch16openalex-snapshot
Harmful Algal Species Fact Sheets
inferred← citeshttps://doi.org/10.1002/9781118994672.ch16bopenalex-snapshot
Harmful Algal Species Fact Sheet: Amphidomataceae
inferred← citeshttps://doi.org/10.1007/978-94-007-6419-4_20openalex-snapshot
Azaspiracid Toxins: Toxicological Profile
inferred← citeshttps://doi.org/10.1007/978-94-007-6650-1_20-1openalex-snapshot
Azaspiracid Toxins: Toxicological Profile
inferred← citeshttps://doi.org/10.1007/s00216-012-5849-2openalex-snapshot
Quantitative analysis of azaspiracids in Azadinium spinosum cultures
inferred← citeshttps://doi.org/10.1007/s00248-021-01777-wopenalex-snapshot
Co-localisation of Azaspiracid Analogs with the Dinoflagellate Species Azadinium spinosum and Amphidoma languida in the Southwest of Ireland
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1007/s40415-017-0435-7openalex-snapshot
First detection of species of the potentially toxic genus Azadinium (Amphidomataceae, Dinophyceae) in tropical coastal waters of Brazil
inferred← citeshttps://doi.org/10.1016/j.aquatox.2012.08.016openalex-snapshot
Effect of Azadinium spinosum on the feeding behaviour and azaspiracid accumulation of Mytilus edulis
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.ecss.2021.107622openalex-snapshot
Insights into the discrepancy between Azadinium spp. and azaspiracid toxins near strategically important aquaculture operations in the west and southwest of Ireland
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.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.2011.06.010openalex-snapshot
The role of Azadinium spinosum (Dinophyceae) in the production of azaspiracid shellfish poisoning in mussels
inferred← citeshttps://doi.org/10.1016/j.hal.2012.05.004openalex-snapshot
Blooms of Azadinium cf. spinosum Elbrächter et Tillmann (Dinophyceae) in northern shelf waters of Argentina, Southwestern Atlantic
inferred← citeshttps://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.
inferred← citeshttps://doi.org/10.1016/j.hal.2012.11.009openalex-snapshot
Morphology, phylogeny and azaspiracid profile of Azadinium poporum (Dinophyceae) from the China Sea
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.hal.2014.04.012openalex-snapshot
Azaspiracid variability of Azadinium poporum (Dinophyceae) from the China Sea
inferred← citeshttps://doi.org/10.1016/j.hal.2014.07.007openalex-snapshot
High abundance of the potentially maitotoxic dinoflagellate Gambierdiscus carpenteri in temperate waters of New South Wales, Australia
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.hal.2016.02.004openalex-snapshot
Growth and bioactive secondary metabolites of arctic Protoceratium reticulatum (Dinophyceae)
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.hal.2016.02.012openalex-snapshot
Toxigenic algae and associated phycotoxins in two coastal embayments in the Ebro Delta (NW Mediterranean)
inferred← citeshttps://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
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.hal.2018.08.003openalex-snapshot
Sympatric occurrence of two Azadinium poporum ribotypes in the Eastern Mediterranean Sea
inferred← citeshttps://doi.org/10.1016/j.hal.2018.08.011openalex-snapshot
Diversity, distribution, and azaspiracids of Amphidomataceae (Dinophyceae) along the Norwegian coast
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.hal.2019.101665openalex-snapshot
The effect of temperature and salinity on growth rate and azaspiracid cell quotas in two strains of Azadinium poporum (Dinophyceae) from Puget Sound, Washington State
inferred← citeshttps://doi.org/10.1016/j.hal.2021.101976openalex-snapshot
Diversity and regional distribution of harmful algal events along the Atlantic margin of Europe
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.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.2023.102471openalex-snapshot
Production of the dinoflagellate Amphidoma languida in a large scale photobioreactor and structure elucidation of its main metabolite AZA-39
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.2026.103196openalex-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.marpolbul.2021.112451openalex-snapshot
DNA metabarcoding illustrates biological pollution threats of Red Sea - Dead Sea water conveyance to Dead Sea biodiversity
inferred← citeshttps://doi.org/10.1016/j.protis.2011.10.005openalex-snapshot
Amphidoma languida sp. nov. (Dinophyceae) Reveals a Close Relationship between Amphidoma and Azadinium
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.toxicon.2012.04.351openalex-snapshot
Azaspiracid accumulation, detoxification and biotransformation in blue mussels (Mytilus edulis) experimentally fed Azadinium spinosum
inferred← citeshttps://doi.org/10.1016/j.toxicon.2012.05.007openalex-snapshot
New azaspiracids in Amphidomataceae (Dinophyceae)
inferred← citeshttps://doi.org/10.1016/j.toxicon.2013.01.010openalex-snapshot
Dissolved azaspiracids are absorbed and metabolized by blue mussels (Mytilus edulis)
inferred← citeshttps://doi.org/10.1016/j.toxicon.2015.10.002openalex-snapshot
Two-year study of lipophilic marine toxin profile in mussels of the North-central Adriatic Sea: First report of azaspiracids in Mediterranean seafood
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.2026.109148openalex-snapshot
Structure elucidation and in vitro toxicity of AZA-40, an azaspiracid isobaric to AZA-1
inferred← citeshttps://doi.org/10.1017/s1755267215001128openalex-snapshot
First records of Amphidoma languida and Azadinium dexteroporum (Amphidomataceae, Dinophyceae) from the Irminger Sea off Iceland
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b01066openalex-snapshot
Chemical Diversity, Origin, and Analysis of Phycotoxins
inferred← citeshttps://doi.org/10.1071/mf19124openalex-snapshot
Field observations of the dinoflagellate genus Azadinium and azaspiracid toxins in the south-west Atlantic Ocean
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/10.1080/09670262.2017.1346205openalex-snapshot
Amphidoma parvula (Amphidomataceae), a new planktonic dinophyte from the Argentine Sea
inferred← citeshttps://doi.org/10.1080/17451000.2013.866252openalex-snapshot
Azadinium caudatumvar.margalefii, a poorly known member of the toxigenic genusAzadinium(Dinophyceae)
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/10.1093/plankt/fbs077openalex-snapshot
Molecular discrimination of taxa within the dinoflagellate genus Azadinium, the source of azaspiracid toxins
inferred← citeshttps://doi.org/10.1093/plankt/fbt054openalex-snapshot
Phycotoxin composition and distribution in plankton fractions from the German Bight and western Danish coast
inferred← citeshttps://doi.org/10.1093/plankt/fbw099openalex-snapshot
Identification ofAzadinium poporum(Dinophyceae) in the Southeast Pacific: morphology, molecular phylogeny, and azaspiracid profile characterization
inferred← citeshttps://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
inferred← citeshttps://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
inferred← citeshttps://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.
inferred← citeshttps://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
inferred← citeshttps://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)
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1111/pre.12455openalex-snapshot
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
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/10.1201/b16662-26openalex-snapshot
AZA: The Producing Organisms—Biology and Trophic Transfer
inferred← citeshttps://doi.org/10.1371/journal.pone.0235015openalex-snapshot
Distribution and abundance of azaspiracid-producing dinophyte species and their toxins in North Atlantic and North Sea waters in summer 2018
inferred← citeshttps://doi.org/10.2216/13-178.1openalex-snapshot
Azadinium dalianense , a new dinoflagellate species from the Yellow Sea, China
inferred← citeshttps://doi.org/10.2216/15-138.1openalex-snapshot
Katodinium glaucum(Dinophyceae) revisited: proposal of new genus, family and order based on ultrastructure and phylogeny
inferred← citeshttps://doi.org/10.3354/ame01603openalex-snapshot
Feeding by heterotrophic protists and copepods on the photosynthetic dinoflagellate Azadinium cf. poporum from western Korean waters
inferred← citeshttps://doi.org/10.3389/frpro.2025.1612811openalex-snapshot
Vertical distribution of harmful algae in the sediment of Uranouchi Inlet by metabarcoding
inferred← citeshttps://doi.org/10.3390/md10061360openalex-snapshot
Production and Isolation of Azaspiracid-1 and -2 from Azadinium spinosum Culture in Pilot Scale Photobioreactors
inferred← citeshttps://doi.org/10.3390/md13116687openalex-snapshot
Structure Elucidation and in Vitro Toxicity of New Azaspiracids Isolated from the Marine Dinoflagellate Azadinium poporum
inferred← citeshttps://doi.org/10.3390/microarrays2010001openalex-snapshot
Testing a Microarray to Detect and Monitor Toxic Microalgae in Arcachon Bay in France
inferred← citeshttps://doi.org/10.3390/microorganisms7080250openalex-snapshot
Metagenomic Sequencing Identifies Highly Diverse Assemblages of Dinoflagellate Cysts in Sediments from Ships’ Ballast Tanks
inferred← citeshttps://doi.org/10.5772/25265openalex-snapshot
Molecular Techniques to Estimate Biodiversity with Case Studies from the Marine Phytoplankton
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