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Identification of Highly Divergent Diatom-Derived Chloroplasts in Dinoflagellates, Including a Description of Durinskia kwazulunatalensis sp. nov. (Peridiniales, Dinophyceae)
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/s002390010210openalex-snapshot
Dinoflagellate Nuclear SSU rRNA Phylogeny Suggests Multiple Plastid Losses and Replacements
inferredcites →https://doi.org/10.1007/s10265-006-0047-yopenalex-snapshot
Description of a new dinoflagellate with a diatom endosymbiont, Durinskia capensis sp. nov. (Peridiniales, Dinophyceae) from South Africa
inferredcites →https://doi.org/10.1007/s10265-012-0486-6openalex-snapshot
Prasinoxanthin is absent in the green-colored dinoflagellate Lepidodinium chlorophorum strain NIES-1868: pigment composition and 18S rRNA phylogeny
inferredcites →https://doi.org/10.1007/s10265-015-0745-4openalex-snapshot
Pigment compositions are linked to the habitat types in dinoflagellates
inferredcites →https://doi.org/10.1016/0303-2647(83)90009-6openalex-snapshot
The functional and phylogenetic significance of dinoflagellate eyespots
inferredcites →https://doi.org/10.1016/j.ejop.2003.11.003openalex-snapshot
Molecular data and the evolutionary history of dinoflagellates
inferredcites →https://doi.org/10.1016/j.ejop.2011.03.001openalex-snapshot
Morphological differences and molecular phylogeny of freshwater blooming species, Peridiniopsis spp. (Dinophyceae) from China
inferredcites →https://doi.org/10.1016/j.protis.2007.04.001openalex-snapshot
An Assessment of Potential Diatom “Barcode” Genes (cox1, rbcL, 18S and ITS rDNA) and their Effectiveness in Determining Relationships in Sellaphora (Bacillariophyta)
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.ympev.2007.03.024openalex-snapshot
Bridging the Rubicon: Phylogenetic analysis reveals repeated colonizations of marine and fresh waters by thalassiosiroid diatoms
inferredcites →https://doi.org/10.1038/22099openalex-snapshot
Single gene circles in dinoflagellate chloroplast genomes
inferredcites →https://doi.org/10.1073/pnas.1421380112openalex-snapshot
Integration of plastids with their hosts: Lessons learned from dinoflagellates
inferredcites →https://doi.org/10.1080/00173139908559217openalex-snapshot
Dinophyte chloroplasts and phylogeny - A review
inferredcites →https://doi.org/10.1080/09670269400650691openalex-snapshot
Ultrastructure of a new marine sand-dwelling dinoflagellate,Gymnodinium quadrilobatumsp. nov. (Dinophyceae) with special reference to its endosymbiotic alga
inferredcites →https://doi.org/10.1093/molbev/msr121openalex-snapshot
MEGA5: Molecular Evolutionary Genetics Analysis Using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods
inferredcites →https://doi.org/10.1093/molbev/msw109openalex-snapshot
Functional Relationship between a Dinoflagellate Host and Its Diatom Endosymbiont
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025647openalex-snapshot
Rampant horizontal transfer and duplication of rubisco genes in eubacteria and plastids
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025808openalex-snapshot
BIONJ: an improved version of the NJ algorithm based on a simple model of sequence data
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026350openalex-snapshot
Phylogenetic Analyses Indicate that the 19′Hexanoyloxy-fucoxanthin-Containing Dinoflagellates Have Tertiary Plastids of Haptophyte Origin
inferredcites →https://doi.org/10.1093/sysbio/syq010openalex-snapshot
New Algorithms and Methods to Estimate Maximum-Likelihood Phylogenies: Assessing the Performance of PhyML 3.0
inferredcites →https://doi.org/10.1098/rstb.2009.0103openalex-snapshot
The endosymbiotic origin, diversification and fate of plastids
inferredcites →https://doi.org/10.1111/j.0022-3646.1973.00091.xopenalex-snapshot
PERIDINIUM BALTICUM (LEVANDER) LEMMERMANN, AN UNUSUAL DINOFLAGELLATE WITH A MESOCARYOTIC AND AN EUCARYOTIC NUCLEUS123
inferredcites →https://doi.org/10.1111/j.0022-3646.1976.00450.xopenalex-snapshot
FURTHER EVIDENCE FOR A MEMBRANE-BOUND ENDOSYMBIONT WITHIN THE DINOFLAGELLATE PERIDINIUM FOLIACEUM1
inferredcites →https://doi.org/10.1111/j.0022-3646.1990.00741.xopenalex-snapshot
LEPIDODINIUM VIRIDE GEN. ET SP. NOV. (GYMNODINAIALES, DINOPHYTA), A GREEN DINOFLAGELLATE WITH A CHLOROPHYLL A‐ AND B‐CONTAINING ENDOSYMBIONT1,2
inferredcites →https://doi.org/10.1111/j.0022-3646.1996.00850.xopenalex-snapshot
IDENTITY OF THE ENDOSYMBIONT OF PERIDINIUM FOLIACEUM (PYRROPHYTA): ANALYSIS OF THE rbcLS OPERON1
inferredcites →https://doi.org/10.1111/j.1440-1835.1996.tb00037.xopenalex-snapshot
The phylogenetic relationship between the Chlamydomonadales and Chlorococcales inferred from 18SrDNA sequence data
inferredcites →https://doi.org/10.1111/j.1440-1835.2006.00426.xopenalex-snapshot
Serial replacement of a diatom endosymbiont in the marine dinoflagellate Peridinium quinquecorne (Peridiniales, Dinophyceae)
inferredcites →https://doi.org/10.1111/j.1529-8817.1976.tb02872.xopenalex-snapshot
FURTHER EVIDENCE FOR A MEMBRANE‐BOUND ENDOSYMBIONT WITHIN THE DINOFLAGELLATEPERIDINIUM FOLIACEUM1
inferredcites →https://doi.org/10.1111/j.1529-8817.2005.00085.xopenalex-snapshot
GALEIDINIIUM RUGATUM GEN. ET SP. NOV. (DINOPHYCEAE), A NEW COCCOID DINOFLAGELLATE WITH A DIATOM ENDOSYMBIONT1
inferredcites →https://doi.org/10.1111/j.1550-7408.1997.tb05672.xopenalex-snapshot
Ribosomal RNA Analysis Indicates a Benthic Pennate Diatom Ancestry for the Endosymbionts of the Dinoflagellates Peridinium foliaceum and Peridinium balticum (Pyrrhophyta)
inferredcites →https://doi.org/10.1111/jpy.12121openalex-snapshot
Global diversity of two widespread, colony‐forming diatoms of the marine plankton, C haetoceros socialis (syn. C . radians) and C haetoceros gelidus sp. nov.
inferredcites →https://doi.org/10.1111/jpy.12135openalex-snapshot
c PPB ‐aE is discovered from photosynthetic benthic dinoflagellates
inferredcites →https://doi.org/10.1127/1864-1318/2014/0159openalex-snapshot
Description of a new freshwater bloom-forming dinoflagellate with a diatom endosymbiont, Peridiniopsis minima sp. nov. (Peridiniales, Dinophyceae) from China
inferredcites →https://doi.org/10.1127/nova_hedwigia/2015/0272openalex-snapshot
Peridiniopsis jiulongensis, a new freshwater dinoflagellate with a diatom endosymbiont from China
inferredcites →https://doi.org/10.1128/ec.00299-13openalex-snapshot
Endosymbiotic Gene Transfer in Tertiary Plastid-Containing Dinoflagellates
inferredcites →https://doi.org/10.1371/journal.pone.0010711openalex-snapshot
The Complete Plastid Genomes of the Two ‘Dinotoms’ Durinskia baltica and Kryptoperidinium foliaceum
inferredcites →https://doi.org/10.1371/journal.pone.0043763openalex-snapshot
Tertiary Endosymbiosis in Two Dinotoms Has Generated Little Change in the Mitochondrial Genomes of Their Dinoflagellate Hosts and Diatom Endosymbionts
inferredcites →https://doi.org/10.1515/botm.1991.34.2.123openalex-snapshot
Ultrastructure of a Marine Dinoflagellate, Peridinium quinquecorne Abé (Peridiniales) from South Africa with Particular Reference to its Chrysophyte Endosymbiont
inferredcites →https://doi.org/10.2216/07-36.1openalex-snapshot
Serial Replacement of Diatom Endosymbionts in Two Freshwater Dinoflagellates, Peridiniopsis spp. (Peridiniales, Dinophyceae)
inferredcites →https://doi.org/10.2216/10-22.1openalex-snapshot
Morphology and SSU rDNA phylogeny ofDurinskia agilis(Kofoid & Swezy) comb. nov. (Peridiniales, Dinophyceae), a thecate, marine, sand-dwelling dinoflagellate formerly classified withinGymnodinium
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.306.4.6zenodo-depositor-declared
Two new generic names for dinophytes harbouring a diatom as an endosymbiont, Blixaea and Unruhdinium (Kryptoperidiniaceae, Peridiniales)
inferred← citeshttps://doi.org/10.1002/9781119842156.ch3openalex-snapshot
Evolution of Plastids and Mitochondria in Diatoms
inferred← citeshttps://doi.org/10.1007/978-1-0716-3726-5_2openalex-snapshot
Complex Endosymbioses I: From Primary to Complex Plastids, Serial Endosymbiotic Events
inferred← citeshttps://doi.org/10.1007/978-1-4939-8654-5_2openalex-snapshot
Complex Endosymbioses I: From Primary to Complex Plastids, Multiple Independent Events
inferred← citeshttps://doi.org/10.1007/978-3-030-92499-7_6openalex-snapshot
Reconstructing Dynamic Evolutionary Events in Diatom Nuclear and Organelle Genomes
inferred← citeshttps://doi.org/10.1007/978-3-031-57446-7_2openalex-snapshot
Complex Plastids Across the Eukaryotes: An Overview of Inherited and Convergently Evolved Characters
inferred← citeshttps://doi.org/10.1007/978-3-031-57446-7_4openalex-snapshot
The Extent, Role, and Timing of Endosymbiotic Gene Transfer in Plastids
inferred← citeshttps://doi.org/10.1007/978-3-031-57446-7_5openalex-snapshot
Easier Lost than Found? What We Know about Plastid Genome Reduction
inferred← citeshttps://doi.org/10.1007/978-3-031-57446-7_6openalex-snapshot
Dinotoms Illuminate Early Pathways to the Stable Acquisition of Photosynthetic Endosymbionts
inferred← citeshttps://doi.org/10.1007/978-3-662-65712-6_5openalex-snapshot
Algae from Secondary Endosymbiosis
inferred← citeshttps://doi.org/10.1007/s00294-017-0761-0openalex-snapshot
Reductive evolution of chloroplasts in non-photosynthetic plants, algae and protists
inferred← citeshttps://doi.org/10.1007/s13127-017-0348-0openalex-snapshot
Absence of co-phylogeny indicates repeated diatom capture in dinophytes hosting a tertiary endosymbiont
inferred← citeshttps://doi.org/10.1016/bs.abr.2017.06.003openalex-snapshot
Secondary Plastids of Stramenopiles
inferred← citeshttps://doi.org/10.1016/bs.abr.2017.06.004openalex-snapshot
Plastid Complexity in Dinoflagellates: A Picture of Gains, Losses, Replacements and Revisions
inferred← citeshttps://doi.org/10.1016/bs.abr.2017.11.015openalex-snapshot
Plastid Genomes in the Myzozoa
inferred← citeshttps://doi.org/10.1016/j.algal.2023.103136openalex-snapshot
Genetic transformation methods for diatom Nitzschia captiva: New tools to better understand dinotom endosymbiosis
inferred← citeshttps://doi.org/10.1016/j.hal.2025.102906openalex-snapshot
High molecular diversity of potentially harmful heterotrophic dinophytes in tropical shrimp aquaculture ponds reveals a new dinophyte Malayana penaeicida gen. et sp. nov. (Peridiniales, Dinophyceae)
inferred← citeshttps://doi.org/10.1016/j.jes.2026.03.037openalex-snapshot
Bloom of Blixaea quinquecornis (Abé) Gottschling (Dinophyceae) with Chaetoceros tenuissimus Meunier in the South Atlantic: Morphology, molecular characterization, and toxins
inferred← citeshttps://doi.org/10.1016/j.protis.2018.04.009openalex-snapshot
Diversity of Organellar Genomes in Non-photosynthetic Diatoms
inferred← citeshttps://doi.org/10.1016/j.protis.2024.126067openalex-snapshot
Dinotoms possess two evolutionary distinct autophagy-related ubiquitin-like conjugation systems
inferred← citeshttps://doi.org/10.1016/j.ympev.2017.10.011openalex-snapshot
Molecular phylogenetics of dinophytes harboring diatoms as endosymbionts (Kryptoperidiniaceae, Peridiniales), with evolutionary interpretations and a focus on the identity of Durinskia oculata from Prague
inferred← citeshttps://doi.org/10.1038/s41396-023-01464-3openalex-snapshot
Prey preference in a kleptoplastic dinoflagellate is linked to photosynthetic performance
inferred← citeshttps://doi.org/10.1038/s41598-019-46852-yopenalex-snapshot
Discovery of a kleptoplastic ‘dinotom’ dinoflagellate and the unique nuclear dynamics of converting kleptoplastids to permanent plastids
inferred← citeshttps://doi.org/10.1038/s41598-023-32949-yopenalex-snapshot
Spatial fragmentation in the distribution of diatom endosymbionts from the taxonomically clarified dinophyte Kryptoperidinium triquetrum (= Kryptoperidinium foliaceum, Peridiniales)
inferred← citeshttps://doi.org/10.1073/pnas.1911884117openalex-snapshot
Dinoflagellates with relic endosymbiont nuclei as models for elucidating organellogenesis
inferred← citeshttps://doi.org/10.1073/pnas.2514821122openalex-snapshot
How to upgrade stolen organelles into permanent plastids: A comparative transcriptomic perspective
inferred← citeshttps://doi.org/10.1080/00318884.2023.2169024openalex-snapshot
Nitzschia captiva sp. nov. (Bacillariophyta), the essential prey diatom of the kleptoplastic dinoflagellateDurinskia capensis, compared withN. agnita, N. kuetzingioidesand other species
inferred← citeshttps://doi.org/10.1080/09670262.2018.1558287openalex-snapshot
Morphology, ultrastructure and molecular phylogeny of cyst-producing Caladoa arcachonensis gen. et sp. nov. (Peridiniales, Dinophyceae) from France and Indonesia
inferred← citeshttps://doi.org/10.1080/09670262.2020.1829078openalex-snapshot
Morphology, ultrastructure and molecular phylogeny of Johsia chumphonensis gen. et sp. nov. and Parvodinium parvulum comb. nov. (Peridiniopsidaceae, Dinophyceae)
inferred← citeshttps://doi.org/10.1093/gbe/evaa096openalex-snapshot
Genomic Insights into Plastid Evolution
inferred← citeshttps://doi.org/10.1093/gbe/evy057openalex-snapshot
Plastid Transcript Editing across Dinoflagellate Lineages Shows Lineage-Specific Application but Conserved Trends
inferred← citeshttps://doi.org/10.1101/2022.07.01.498404openalex-snapshot
Insight into diatoms diversity at two European coastal sites (LTER-MC in the Mediterranean Sea and SOMLIT-Astan in the Western English Channel) using a DNA Metabarcoding approach
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/jpy.12824openalex-snapshot
The complete chloroplast and mitochondrial genomes of the diatomNitzschia palea(Bacillariophyceae) demonstrate high sequence similarity to the endosymbiont organelles of the dinotomDurinskia baltica
inferred← citeshttps://doi.org/10.1111/jpy.13039openalex-snapshot
Convergence in the RNA processing of fractured algal organelle genomes
inferred← citeshttps://doi.org/10.1111/pre.12473openalex-snapshot
Sterols of the ‘dinotom’ Durinskia baltica (Dinophyceae) are of dinoflagellate origin
inferred← citeshttps://doi.org/10.1128/mmbr.00197-22openalex-snapshot
Adaptations and metabolic evolution of myzozoan protists across diverse lifestyles and environments
inferred← citeshttps://doi.org/10.17129/botsci.3259openalex-snapshot
Timescale lessons of Durinskia baltica (Kryptoperidiniaceae, Dinophyta) from freshwater through a molecular phylogeny
inferred← citeshttps://doi.org/10.21685/1680-0826-2020-14-2-2openalex-snapshot
A Kryptoperidiniaceae species (Dinophyceae: Peridiniales) blooming in coastal Yucatan waters, Gulf of Mexico
inferred← citeshttps://doi.org/10.2216/17-140.1openalex-snapshot
Ultrastructure and phylogeny of a new species of mixotrophic dinoflagellate,Paragymnodinium stigmaticum sp. nov. (Gymnodiniales, Dinophyceae)
inferred← citeshttps://doi.org/10.22201/fc.24488100e.2021.7.2.1openalex-snapshot
Bibliometric analysis of global trends in the study of the evolutionary history of chloroplasts in members of the Class Dinophyceae
inferred← citeshttps://doi.org/10.24275/lshu4081openalex-snapshot
Durinskia yucatanensis sp. nov. (Peridiniales: Kryptoperidiniaceae), a new planktonic dinoflagellate species, and its habitat in coastal Yucatan waters, Gulf of Mexico
inferred← citeshttps://doi.org/10.24275/uam/izt/dcbs/hidro/2022v32n3/liraopenalex-snapshot
Historical revision of generic and specific nomenclatural changes of Durinskia baltica (Dinophyceae: Peridiniales)
inferred← citeshttps://doi.org/10.3389/fmicb.2018.02289openalex-snapshot
Insight Into the Pico- and Nano-Phytoplankton Communities in the Deepest Biosphere, the Mariana Trench
inferred← citeshttps://doi.org/10.3389/fpls.2020.591050openalex-snapshot
Five Non-motile Dinotom Dinoflagellates of the Genus Dinothrix
inferred← citeshttps://doi.org/10.3389/fpls.2022.918543openalex-snapshot
Comparative Plastid Genomics of Green-Colored Dinoflagellates Unveils Parallel Genome Compaction and RNA Editing
inferred← citeshttps://doi.org/10.3389/fpls.2023.1226027openalex-snapshot
Circadian rhythms and circadian clock gene homologs of complex alga Chromera velia
inferred← citeshttps://doi.org/10.3389/fpls.2026.1766966openalex-snapshot
Photosynthetic and nutritional plasticity in mixotrophic dinoflagellates: responses to environmental change
inferred← citeshttps://doi.org/10.3390/jmse11101903openalex-snapshot
Complex Plastids and the Evolution of the Marine Phytoplankton
inferred← citeshttps://doi.org/10.3390/md20090581openalex-snapshot
A Comparison of Dinoflagellate Thiolation Domain Binding Proteins Using In Vitro and Molecular Methods
inferred← citeshttps://doi.org/10.3390/phycology2040022openalex-snapshot
Preservation of Dinoflagellate Cysts in Different Oxygen Regimes: Differences in Cyst Survival between Oxic and Anoxic Natural Environments
inferred← citeshttps://doi.org/10.4081/jlimnol.2021.2023openalex-snapshot
The first floristic study of freshwater dinoflagellates (Dinophyceae) in Colombia
inferred← citeshttps://doi.org/10.4490/algae.2021.36.5.25openalex-snapshot
Plastid-associated galactolipid composition in eyespot-containing dinoflagellates: a review
inferred← citeshttps://doi.org/10.64898/2026.05.20.726455openalex-snapshot
Mechanistic Constraints on ClpM Expression Underlie Apicoplast Genome Retention in Malaria Parasites
inferred← citeshttps://doi.org/10.64898/2026.06.22.732937openalex-snapshot
Single cell genomics and fluorescence microscopy suggest a permanent plastid in a marine centrohelid
inferred← citeshttps://doi.org/10.70675/e80da54ez4400z4af2z90ccza6b6fb5b6bc7openalex-snapshot
Origins and early evolution of photosynthetic eukaryotes
inferred← citeshttps://doi.org/10.7554/elife.23717openalex-snapshot
Chimeric origins of ochrophytes and haptophytes revealed through an ancient plastid proteome
inferred← citeshttps://doi.org/10.7717/peerj.12220openalex-snapshot
Nitzschia anatoliensis sp. nov., a cryptic diatom species from the highly alkaline Van Lake (Turkey)
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