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Taxonomic Studies of Ciona intestinalis (L.) and Its Allies
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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/bf02955974openalex-snapshot
Die Stammverwandtschaft zwischen Ascidien und Wirbelthieren
inferredcites →https://doi.org/10.1016/0300-9629(84)90148-8openalex-snapshot
Comparative study on amounts of trace elements in the solitary ascidians, Ciona intestinalis and Ciona robusta
inferredcites →https://doi.org/10.1080/00222936308681401openalex-snapshot
XVIII.—Observations on the British Tunicata, with descriptions of several new species
inferredcites →https://doi.org/10.1080/00222937008696269openalex-snapshot
XXXIV.—On the larval state of Molgula; with descriptions of several new species of Simple Ascidians
inferredcites →https://doi.org/10.1111/j.1096-3642.1970.tb00732.xopenalex-snapshot
Ascidians, including specimens from the deep sea, collected by the R.V. ‘Vema’ and now in the American Museum of Natural History
inferredcites →https://doi.org/10.1111/j.1469-7998.1963.tb01623.xopenalex-snapshot
AUSTRALIAN ASCIDIANS IN THE BRITISH MUSEUM (NATURAL HISTORY)
inferredcites →https://doi.org/10.5134/175476openalex-snapshot
AN UNUSUALLY ROBUST CIONA FROM THE NORTHEASTERN COAST OF HONSYU ISLAND, JAPAN
inferredcites →https://doi.org/10.5281/zenodo.13449581openalex-snapshot
Ein Beitrag zur Kenntnis der japanischen Ascidienfauna
inferredcites →https://doi.org/10.5281/zenodo.16136963openalex-snapshot
Observations on the British Tunicata with descriptions of several new species
inferredcites →https://doi.org/10.5281/zenodo.16553898openalex-snapshot
Die einfachen Ascidien (Ascidiae Simplices) des Golfes von Neapel
inferredcites →https://doi.org/10.5479/si.00963801.45-1989.427openalex-snapshot
The simple ascidians from the northeastern Pacific in the collection of the United States National Museum
inferredcites →https://doi.org/10.5962/bhl.title.125513openalex-snapshot
Mémoires sur les animaux sans vertèbres. *1e partie*@Description et classification des animaux invertébrés et articulés, connus sous les noms de crustacés, d'insectes, d'annélides, etc
inferredcites →https://doi.org/10.5962/bhl.title.1573openalex-snapshot
The ascidians collected by the United States fisheries bureau steamer Albatross on the coast of California during the summer of 1904
inferredcites →https://doi.org/10.5962/bhl.title.65971openalex-snapshot
Mémoires sur les animaux sans vertèbres /
inferredcites →https://doi.org/10.5962/bhl.title.69327openalex-snapshot
Northern and Arctic invertebrates in the collection of the Swedish State Museum (Riksmuseum).
inferredcites →https://doi.org/10.5962/p.260426openalex-snapshot
Ascidies récoltées par la «Thalassa» sur la pente du plateau continental du Golfe de Gascogne (18-25 octobre 1968)
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/zootaxa.4657.3.1zenodo-depositor-declared
The Ascidiacea collected during the 2017 British Columbia Hakai MarineGEO BioBlitz
inferred← citeshttps://doi.org/10.5281/zenodo.4525060openalex-extracted
New records of ascidians from the NE Pacific: a new species of Trididemnum, range extension and redescription of Aplidiopsis pannosum (Ritter, 1899) including its larva, and several non-indigenous species
inferred← citeshttps://doi.org/10.1002/(sici)1098-2795(200001)55:1<109::aid-mrd15>3.0.co;2-bopenalex-snapshot
Mechanism of the block to hybridization and selfing between the sympatric ascidians Ciona intestinalis and Ciona savignyi
inferred← citeshttps://doi.org/10.1002/dvdy.21163openalex-snapshot
Initial stage of genetic mapping in Ciona intestinalis
inferred← citeshttps://doi.org/10.1002/dvg.22837openalex-snapshot
Mutation studies in ascidians: A review
inferred← citeshttps://doi.org/10.1002/jez.1402410109openalex-snapshot
Autonomous fluorescence of eggs of the ascidian Ciona intestinalis
inferred← citeshttps://doi.org/10.1002/jez.1402420212openalex-snapshot
Differentiation of the accessory cells and structural regionalization of the oocyte in the ascidian Ciona savignyi during early oogenesis
inferred← citeshttps://doi.org/10.1007/978-3-642-20763-1_6openalex-snapshot
A New Animal Model for Merging Ecology and Evolution
inferred← citeshttps://doi.org/10.1007/978-4-431-56432-4_26openalex-snapshot
Taxonomy of Ascidians (Urochordata: Ascidiacea) in Japan: Past, Present, and Future
inferred← citeshttps://doi.org/10.1007/bf00539896openalex-snapshot
Regulated spatial expression of fusion gene constructs with the 5? upstream region of Halocynthia roretzi muscle actin gene in Ciona savignyi embryos
inferred← citeshttps://doi.org/10.1007/s00227-007-0617-0openalex-snapshot
Genealogical relationships within and among shallow-water Ciona species (Ascidiacea)
inferred← citeshttps://doi.org/10.1007/s00227-012-1898-5openalex-snapshot
Field identification of ‘types’ A and B of the ascidian Ciona intestinalis in a region of sympatry
inferred← citeshttps://doi.org/10.1007/s00239-003-2559-6openalex-snapshot
Complete mtDNA of Ciona intestinalis Reveals Extensive Gene Rearrangement and the Presence of an atp8 and an Extra trnM Gene in Ascidians
inferred← citeshttps://doi.org/10.1007/s00239-005-0009-3openalex-snapshot
Genomic Approaches Reveal Unexpected Genetic Divergence Within Ciona intestinalis
inferred← citeshttps://doi.org/10.1007/s00438-009-0453-7openalex-snapshot
DrosophilaP transposons of the urochordata Ciona intestinalis
inferred← citeshttps://doi.org/10.1007/s101260000048openalex-snapshot
Genetic Relatedness and Variability in Inbred and Wild Populations of the Solitary Ascidian Ciona intestinalis Revealed by Arbitrarily Primed Polymerase Chain Reaction
inferred← citeshttps://doi.org/10.1007/s12526-017-0699-yopenalex-snapshot
The invasive ascidian Ciona robusta recorded from a Red Sea marina
inferred← citeshttps://doi.org/10.1007/s12526-025-01534-zopenalex-snapshot
Novel insights into the phylogeographic patterns of ascidians fouling Greek mussel cultures
inferred← citeshttps://doi.org/10.1007/s12601-019-0041-7openalex-snapshot
Assessing Cryptic Invasion State: Fine-Scale Genetic Analysis of Ciona savignyi Population in Putative Native Habitat of the Korean Coast
inferred← citeshttps://doi.org/10.1007/s42995-024-00228-yopenalex-snapshot
Context-dependent antioxidant defense system (ADS)-based stress memory in response to recurrent environmental challenges in congeneric invasive species
inferred← citeshttps://doi.org/10.1016/0012-1606(88)90178-9openalex-snapshot
Development of myoplasm-enriched ascidian embryos
inferred← citeshttps://doi.org/10.1016/j.bse.2005.03.011openalex-snapshot
Qualitative variation of alkaloids in color morphs of Cystodytes (Ascidiacea)
inferred← citeshttps://doi.org/10.1016/j.gene.2015.09.066openalex-snapshot
Reference gene selection for quantitative gene expression studies during biological invasions: A test on multiple genes and tissues in a model ascidian Ciona savignyi
inferred← citeshttps://doi.org/10.1016/j.jembe.2016.09.001openalex-snapshot
Comparative morpho-physiological analysis between Ciona robusta and Ciona savignyi
inferred← citeshttps://doi.org/10.1016/j.marenvres.2014.06.006openalex-snapshot
Marine fouling invasions in ports of Patagonia (Argentina) with implications for legislation and monitoring programs
inferred← citeshttps://doi.org/10.1016/j.ydbio.2019.10.028openalex-snapshot
Hox13 is essential for formation of a sensory organ at the terminal end of the sperm duct in Ciona
inferred← citeshttps://doi.org/10.1016/j.ympev.2010.03.042openalex-snapshot
Polymorphism and divergence within the ascidian genus Ciona
inferred← citeshttps://doi.org/10.1016/j.ympev.2011.11.013openalex-snapshot
Peculiar patterns of amino acid substitution and conservation in the fast evolving tunicate Oikopleura dioica
inferred← citeshttps://doi.org/10.1017/s175526720900116xopenalex-snapshot
Reinclusion of Ciona intestinalis (Ascidiacea: Cionidae) in Brazil—a methodological view
inferred← citeshttps://doi.org/10.1038/s41598-020-68031-0openalex-snapshot
Coupling feeding activity, growth rates and molecular data shows dietetic needs of Ciona robusta (Ascidiacea, Phlebobranchia) in automatic culture plants
inferred← citeshttps://doi.org/10.1038/srep24875openalex-snapshot
Contrasting global genetic patterns in two biologically similar, widespread and invasive Ciona species (Tunicata, Ascidiacea)
inferred← citeshttps://doi.org/10.1073/pnas.0610158104openalex-snapshot
Cryptic speciation in a model invertebrate chordate
inferred← citeshttps://doi.org/10.1079/cabicompendium.88555openalex-snapshot
Ciona intestinalis (sea vase)
inferred← citeshttps://doi.org/10.1080/00785326.1998.10409376openalex-snapshot
Ascidians from the north-western Pacific Region. 5. Phlebobranchia.
inferred← citeshttps://doi.org/10.1080/24750263.2026.2718662openalex-snapshot
Challenge from nomenclature changes: the case of ascidian biodiversity
inferred← citeshttps://doi.org/10.1086/719476openalex-snapshot
Ecological Review of the Ciona Species Complex
inferred← citeshttps://doi.org/10.1093/gbe/evu122openalex-snapshot
Evolutionary Genomics of Fast Evolving Tunicates
inferred← citeshttps://doi.org/10.1093/zoolinnean/zlaa042openalex-snapshot
An integrative taxonomic framework for the study of the genus Ciona (Ascidiacea) and description of a new species, Ciona intermedia
inferred← citeshttps://doi.org/10.1111/j.1440-169x.1987.00627.xopenalex-snapshot
Cytological Characterization of Self Incompatibility in Gametes of the Ascidian, Ciona intestinalis
inferred← citeshttps://doi.org/10.1111/j.1440-169x.1991.00307.xopenalex-snapshot
Gray and Red Fragments of the Egg of the Ascidian Ciona savignyi: Preferential Development of Muscle Cells from Gray Fragments
inferred← citeshttps://doi.org/10.1111/j.1463-6409.2005.00167.xopenalex-snapshot
How do morphotypes and chemotypes relate to genotypes? The colonial ascidianCystodytes(Polycitoridae)
inferred← citeshttps://doi.org/10.1111/jzs.12101openalex-snapshot
Morphological evidence that the molecularly determinedCiona intestinalistype A and type B are different species:Ciona robustaandCiona intestinalis
inferred← citeshttps://doi.org/10.1111/maec.12543openalex-snapshot
Temporal correlation of population composition and environmental variables in the marine invader Ciona robusta
inferred← citeshttps://doi.org/10.1111/mec.14382openalex-snapshot
Rapid response to changing environments during biological invasions: DNA methylation perspectives
inferred← citeshttps://doi.org/10.1134/s1063074007020083openalex-snapshot
On the introduction of the ascidian Ciona savignyi Herdman, 1882 into Peter the Great Bay, Sea of Japan
inferred← citeshttps://doi.org/10.1371/journal.pone.0122879openalex-snapshot
Morphological Differences between Larvae of the Ciona intestinalis Species Complex: Hints for a Valid Taxonomic Definition of Distinct Species
inferred← citeshttps://doi.org/10.15298/invertzool.11.1.04openalex-snapshot
Deep-sea fauna of European seas: An annotated species check-list of benthic invertebrates living deeper than 2000 m in the seas bordering Europe. Ascidiacea
inferred← citeshttps://doi.org/10.1530/rep-24-0184openalex-snapshot
An attempt to search for the common cellular mechanism of ovulation across all metazoans
inferred← citeshttps://doi.org/10.15368/theses.2012.31openalex-snapshot
THE PROTEOMIC RESPONSE OF SEA SQUIRTS (GENUS CIONA CONGENERS) TO HYPOSALINITY STRESS
inferred← citeshttps://doi.org/10.2108/zsj.21.285openalex-snapshot
Development of Ciona intestinalis Juveniles (Through 2nd Ascidian Stage)
inferred← citeshttps://doi.org/10.2307/1541299openalex-snapshot
CHANGES IN BEHAVIOR AND OCELLAR STRUCTURE DURING THE LARVAL LIFE OF SOLITARY ASCIDIANS
inferred← citeshttps://doi.org/10.2307/1541632openalex-snapshot
THE ACCUMULATION AND DISTRIBUTION OF VANADIUM, IRON, AND MANGANESE IN SOME SOLITARY ASCIDIANS
inferred← citeshttps://doi.org/10.2988/0006-324x-127.1.284openalex-snapshot
Morphological and molecular identification of an introduced alien sea squirt (Tunicata: Ascidiacea) in Korea
inferred← citeshttps://doi.org/10.3354/meps259145openalex-snapshot
Persistence and differential distribution of nonindigenous ascidians in harbors of the Southern California Bight
inferred← citeshttps://doi.org/10.3391/ai.2010.5.4.05openalex-snapshot
First record of the solitary ascidian Ciona savignyi Herdman, 1882 in the Southern Hemisphere
inferred← citeshttps://doi.org/10.3391/ai.2012.7.3.002openalex-snapshot
Barcoding of the cytochrome oxidase I (COI) indicates a recent introduction of Ciona savignyi into New Zealand and provides a rapid method for Ciona species discrimination
inferred← citeshttps://doi.org/10.3391/bir.2020.9.3.01openalex-snapshot
Iceland: a laboratory for non-indigenous ascidians
inferred← citeshttps://doi.org/10.4282/sosj.29.61openalex-snapshot
Recent topics on the biology of alien ascidians
inferred← citeshttps://doi.org/10.5179/benthos.80.62openalex-snapshot
Marine nonnative species in Japanese waters: Results of the two questionnaire surveys conducted in 2002–2003 and 2022–2023
inferred← citeshttps://doi.org/10.5179/benthos1981.1986.44openalex-snapshot
Several recent studies on the ascidian species: a brief review
inferred← citeshttps://doi.org/10.5962/p.289566openalex-snapshot
Ascidies de Nouvelle-Calédonie VIII. Phlébobranches (suite)
inferred← citeshttps://doi.org/10.70675/6bac8de3z0b88z4e0dzbec7za7f96e119214openalex-snapshot
Divergence évolutive et isolement reproducteur chez les ascidies du genre Ciona, introduites et indigènes en Europe
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