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Identification ofAzadinium poporum(Dinophyceae) in the Southeast Pacific: morphology, molecular phylogeny, and azaspiracid profile characterization

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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/bf00160155openalex-snapshot

Estimation of evolutionary distances between nucleotide sequences

inferredcites →https://doi.org/10.1007/bf01731581openalex-snapshot

A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences

inferredcites →https://doi.org/10.1007/bf01734359openalex-snapshot

Evolutionary trees from DNA sequences: A maximum likelihood approach

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/10.1007/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/10.1016/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.hal.2012.05.004openalex-snapshot

Blooms of Azadinium cf. spinosum Elbrächter et Tillmann (Dinophyceae) in northern shelf waters of Argentina, Southwestern Atlantic

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.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.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.seares.2011.03.008openalex-snapshot

Bloom of the Yessotoxin producing dinoflagellate Protoceratium reticulatum (Dinophyceae) in Northern Chile

inferredcites →https://doi.org/10.1016/j.toxicon.2006.11.013openalex-snapshot

Identification of pectenotoxins in plankton, filter feeders, and isolated cells of a Dinophysis acuminata with an atypical toxin profile, from Chile

inferredcites →https://doi.org/10.1016/j.toxicon.2008.03.022openalex-snapshot

Confirmation by LC–MS/MS of azaspiracids in shellfish from the Portuguese north-western coast

inferredcites →https://doi.org/10.1016/j.toxicon.2008.05.006openalex-snapshot

First report on azaspiracid and yessotoxin groups detection in French shellfish

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.2009.04.013openalex-snapshot

Pectenotoxins and yessotoxin from Arica Bay, North Chile as determined by tandem mass spectrometry

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/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.2011.07.006openalex-snapshot

Latitudinal transects in the southeastern Pacific Ocean reveal a diverse but patchy distribution of phycotoxins

inferredcites →https://doi.org/10.1016/j.toxicon.2012.05.007openalex-snapshot

New azaspiracids in Amphidomataceae (Dinophyceae)

inferredcites →https://doi.org/10.1016/j.toxicon.2014.07.017openalex-snapshot

Lipophilic toxins in cultivated mussels (Mytilus galloprovincialis) from Baja California, Mexico

inferredcites →https://doi.org/10.1016/j.toxicon.2015.05.010openalex-snapshot

Occurrence and profiles of lipophilic toxins in shellfish harvested from Argentina

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(03)00105-3openalex-snapshot

The first identification of azaspiracids in shellfish from France and Spain

inferredcites →https://doi.org/10.1021/np500555kopenalex-snapshot

Isolation, Structure Elucidation, Relative LC-MS Response, and in Vitro Toxicity of Azaspiracids from the Dinoflagellate Azadinium spinosum

inferredcites →https://doi.org/10.1023/a:1008027610826openalex-snapshot

Copper, copper mine tailings and their effect on marine algae in Northern Chile

inferredcites →https://doi.org/10.1051/alr/2009028openalex-snapshot

Paralytic shellfish toxins inArgopecten purpuratusandSemimytilus algosusfrom northern Chile

inferredcites →https://doi.org/10.1073/pnas.1012021107openalex-snapshot

Navigating transformations in governance of Chilean marine coastal resources

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/10.1093/bioinformatics/17.8.754openalex-snapshot

MRBAYES: Bayesian inference of phylogenetic trees

inferredcites →https://doi.org/10.1093/molbev/mst197openalex-snapshot

MEGA6: Molecular Evolutionary Genetics Analysis Version 6.0

inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot

MUSCLE: multiple sequence alignment with high accuracy and high throughput

inferredcites →https://doi.org/10.1093/plankt/fbq022openalex-snapshot

Intra- and interannual variability of nearshore phytoplankton biovolume and community changes in the northern Humboldt Current system

inferredcites →https://doi.org/10.1093/plankt/fbs077openalex-snapshot

Molecular discrimination of taxa within the dinoflagellate genus Azadinium, the source of azaspiracid toxins

inferredcites →https://doi.org/10.1111/j.0022-3646.1985.00347.xopenalex-snapshot

THE Si:C:N RATIO OF MARINE DIATOMS: INTERSPECIFIC VARIABILITY AND THE EFFECT OF SOME ENVIRONMENTAL VARIABLES 1

inferredcites →https://doi.org/10.1111/j.0022-3646.1994.00999.xopenalex-snapshot

IDENTIFICATION OF GROUP‐ AND STRAIN‐SPECIFIC GENETIC MARKERS FOR GLOBALLY DISTRIBUTED ALEXANDRIUM (DINOPHYCEAE). II. SEQUENCE ANALYSIS OF A FRAGMENT OF THE LSU rRNA GENE 1

inferredcites →https://doi.org/10.1111/j.0022-3646.1996.00424.xopenalex-snapshot

ANALYSIS OF ALEXANDRIUM (DINOPHYCEAE) SPECIES USING SEQUENCES OF THE 5.8S RIBOSOMAL DNA AND INTERNAL TRANSCRIBED SPACER REGIONS1

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.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/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/10.1128/aem.54.6.1426-1429.1988openalex-snapshot

Extraction from Natural Planktonic Microorganisms of DNA Suitable for Molecular Biological Studies

inferredcites →https://doi.org/10.1201/b16569-3openalex-snapshot

Harmful Algae and their Toxins: Progress, Paradoxes and Paradigm Shifts

inferredcites →https://doi.org/10.1201/b16662openalex-snapshot

Seafood and Freshwater Toxins

inferredcites →https://doi.org/10.1201/b16662-26openalex-snapshot

AZA: The Producing Organisms—Biology and Trophic Transfer

inferredcites →https://doi.org/10.1201/b16662-28openalex-snapshot

Azaspiracids: Toxicology, Pharmacology, and Risk Assessment

inferredcites →https://doi.org/10.1201/b16662-31openalex-snapshot

Gambierol: Synthetic Aspects

inferredcites →https://doi.org/10.1201/b16662-33openalex-snapshot

Cyclic Imine Toxins: Chemistry, Origin, Metabolism, Pharmacology, Toxicology, and Detection

inferredcites →https://doi.org/10.1271/bbb.61.1775openalex-snapshot

Fluorometric Measurement of Yessotoxins in Shellfish by High-pressure Liquid Chroraatography

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/10.2983/0730-8000(2006)25[1067:fdoaim]2.0.co;2openalex-snapshot

FIRST DETECTION OF AZASPIRACIDS IN MUSSELS IN NORTH WEST AFRICA

inferredcites →https://doi.org/10.3354/meps197041openalex-snapshot

Primary production and community respiration in the Humboldt Current System off Chile and associated oceanic areas

inferredcites →https://doi.org/10.3354/meps269083openalex-snapshot

Phytoplankton size structure during and after the 1997/98 El Niño in a coastal upwelling area of the northern Humboldt Current System

inferredcites →https://doi.org/10.3390/md11061815openalex-snapshot

Diarrhetic Shellfish Toxins and Other Lipophilic Toxins of Human Health Concern in Washington State

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/10.3724/sp.j.1123.2010.00363openalex-snapshot

Determination of azaspiracid-1 in shellfishes by liquid chromatography with tandem mass spectrometry

inferredcites →https://doi.org/10.4067/s0718-19572012000300016openalex-snapshot

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

inferredcites →https://doi.org/10.4067/s0718-19572014000300008openalex-snapshot

Azadinium (Amphidomataceae, Dinophyceae) in the Southwest Atlantic: In situ and satellite observations

inferredcites →https://doi.org/10.4319/lo.1997.42.5_part_2.1137openalex-snapshot

Harmful algal blooms: Their ecophysiology and general relevance to phytoplankton blooms in the sea

What points at this work

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

inferred← citeshttps://doi.org/10.1080/00318884.2024.2382521zenodo-depositor-declared

Morphological and molecular characterization of Prorocentrum bidens (formerly known as P. compressum ) and description of the closely related Prorocentrum bisaeptum sp. nov . (Prorocentrales, Dinophyceae)

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.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.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.2018.12.005openalex-snapshot

Two novel azaspiracids from Azadinium poporum, and a comprehensive compilation of azaspiracids produced by Amphidomataceae, (Dinophyceae)

inferred← citeshttps://doi.org/10.1016/j.hal.2019.05.003openalex-snapshot

Cryptic speciation in Protoceratium reticulatum (Dinophyceae): Evidence from morphological, molecular and ecophysiological data

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.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.toxcx.2020.100059openalex-snapshot

Fatty acid esters of azaspiracids identified in mussels (Mytilus edulis) using liquid chromatography-high resolution 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/10.1080/00318884.2023.2204681openalex-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/10.1080/09670262.2021.1948614openalex-snapshot

Clarifying confusion – Prorocentrum triestinum J.Schiller and Prorocentrum redfieldii Bursa (Prorocentrales, Dinophyceae) are two different species

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/10.3390/md17090489openalex-snapshot

Effects of Temperature, Growth Media, and Photoperiod on Growth and Toxin Production of Azadinium spinosum

inferred← citeshttps://doi.org/10.3390/microorganisms9010134openalex-snapshot

Multiple New Strains of Amphidomataceae (Dinophyceae) from the North Atlantic Revealed a High Toxin Profile Variability of Azadinium spinosum and a New Non-Toxigenic Az. cf. spinosum

inferred← citeshttps://doi.org/10.3390/toxins12090564openalex-snapshot

A Mediterranean Alexandrium taylorii (Dinophyceae) Strain Produces Goniodomin A and Lytic Compounds but Not Paralytic Shellfish Toxins

inferred← citeshttps://doi.org/10.5194/bg-22-3397-2025openalex-snapshot

Extraordinary bloom of toxin-producing phytoplankton enhanced by strong retention on the offshore Patagonian shelf

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