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Azadinium obesum (Dinophyceae), a new nontoxic species in the genus that can produce azaspiracid toxins

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What this work says

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

inferredcites →https://doi.org/10.1002/rcm.3385openalex-snapshot

Discovery of new analogs of the marine biotoxin azaspiracid in blue mussels ( Mytilus edulis ) by ultra‐performance liquid chromatography/tandem mass spectrometry

inferredcites →https://doi.org/10.1007/s00216-008-2221-7openalex-snapshot

LC-MS-MS aboard ship: tandem mass spectrometry in the search for phycotoxins and novel toxigenic plankton from the North Sea

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/s0041-0101(01)00226-4openalex-snapshot

Chronic effects in mice caused by oral administration of sublethal doses of azaspiracid, a new marine toxin isolated from mussels

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(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/10.1080/0967026031000096227openalex-snapshot

Discrimination of the toxigenic dinoflagellates Alexandrium tamarense and A. ostenfeldii in co-occurring natural populations from Scottish coastal waters

inferredcites →https://doi.org/10.1080/09670260601044068openalex-snapshot

An assessment of cryptic genetic diversity within theCyclotella meneghinianaspecies complex (Bacillariophyta) based on nuclear and plastid genes, and amplified fragment length polymorphisms

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/10.1093/plankt/3.1.53openalex-snapshot

A survey for body scales in dinoflagellates and a revision of Cachonina and Heterocapsa (Pyrrhophyta)

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.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/10.2216/i0031-8884-20-4-424.1openalex-snapshot

A scanning electron microscopical study of the apical pores of marine dinoflagellates (Dinophyceae)

inferredcites →https://doi.org/10.2216/i0031-8884-42-4-420.1openalex-snapshot

Chemical ecology of eukaryotic microalgae in marine ecosystems

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

inferredcites →https://doi.org/10.5860/choice.35-3284openalex-snapshot

Identifying marine phytoplankton

What points at this work

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

inferred← citeshttps://doi.org/10.11646/phytotaxa.220.3.3zenodo-depositor-declared

Taxonomic clarification of the dinophyte Peridinium acuminatum Ehrenb., ≡ Scrippsiella acuminata, comb. nov. (Thoracosphaeraceae, Peridiniales)

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/s00216-015-8637-yopenalex-snapshot

Quantification and profiling of lipophilic marine toxins in microalgae by UHPLC coupled to high-resolution orbitrap mass spectrometry

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/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/s12526-016-0471-8openalex-snapshot

Dinoflagellate taxonomy — a review and proposal of a revised classification

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.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.fct.2019.04.041openalex-snapshot

Bioaccessibility of lipophilic and hydrophilic marine biotoxins in seafood: An in vitro digestion approach

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.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.2018.08.011openalex-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.2019.101697openalex-snapshot

Ocean acidification increases domoic acid contents during a spring to summer succession of coastal phytoplankton

inferred← citeshttps://doi.org/10.1016/j.hal.2020.101874openalex-snapshot

Temporal and spatial distribution of Azadinium species in the inland and coastal waters of the Pacific northwest in 2014–2018

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.2025.102969openalex-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.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.protis.2017.08.001openalex-snapshot

Ultrastructure and Phylogeny of Kirithra asteri gen. et sp. nov. (Ceratoperidiniaceae, Dinophyceae) — a Free-Living, Thin-Walled Marine Photosynthetic Dinoflagellate from Argentina

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.2017.07.025openalex-snapshot

Presence of azaspiracids in bivalve molluscs from Northern Spain

inferred← citeshttps://doi.org/10.1016/j.toxicon.2017.11.001openalex-snapshot

Assessing the presence of marine toxins in bivalve molluscs from southwest India

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/10.1021/tx200553popenalex-snapshot

Comparative Effects of the Marine Algal Toxins Azaspiracid-1, -2, and -3 on Jurkat T Lymphocyte Cells

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/10.1080/00318884.2019.1670013openalex-snapshot

Amphidomataceae (Dinophyceae) in the western Greenland area, including description of Azadinium perforatum sp. nov.

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/10.1080/09670262.2011.556753openalex-snapshot

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

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/fby052openalex-snapshot

Molecular detection and quantification of the azaspiracid-producing dinoflagellateAmphidoma languida(Amphidomataceae, Dinophyceae)

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/jpy.12584openalex-snapshot

Plate pattern clarification of the marine dinophyte Heterocapsa triquetra sensu Stein (Dinophyceae) collected at the Kiel Fjord (Germany)

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.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.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/10.1201/b16662-26openalex-snapshot

AZA: The Producing Organisms—Biology and Trophic Transfer

inferred← citeshttps://doi.org/10.13057/biodiv/d221156openalex-snapshot

Detection of marine microalgae (phytoplankton) quality to support seafood health: A case study on the west coast of South Sulawesi, Indonesia

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/10.3354/ame01603openalex-snapshot

Feeding by heterotrophic protists and copepods on the photosynthetic dinoflagellate Azadinium cf. poporum from western Korean waters

inferred← citeshttps://doi.org/10.3390/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/10.3906/bot-1506-34openalex-snapshot

First molecular records of potentially harmful planktonic dinoflagellatesfrom the southern Black Sea

inferred← citeshttps://doi.org/10.4067/s0718-19572012000300016openalex-snapshot

A new record of Azadinium spinosum (Dinoflagellata) from the tropical Mexican Pacific

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