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Central control of swimming in the cubomedusan jellyfishCarybdea rastonii
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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/jcp.1030220306openalex-snapshot
Neuromuscular facilitation in scyphomedusae
inferredcites →https://doi.org/10.1002/jez.1401900103openalex-snapshot
Morphological substrates of conduction in the colonial hydroid Hydractinia echinata. I. An ectodermal nerve net
inferredcites →https://doi.org/10.1002/jmor.1051230105openalex-snapshot
The recognition, distribution and ultrastructure of hydrozoan nerve elements
inferredcites →https://doi.org/10.1002/neu.480060403openalex-snapshot
Neurobiology of Stomotoca. II. Pacemakers and conduction pathways
inferredcites →https://doi.org/10.1002/neu.480090205openalex-snapshot
Neurobiology of Polyorchis. I. Function of effector systems
inferredcites →https://doi.org/10.1007/978-1-4757-9724-4_67openalex-snapshot
The Control of Fast and Slow Muscle Contractions in the Siphonophore Stem
inferredcites →https://doi.org/10.1007/bf00593116openalex-snapshot
Unit spike activity in the coelenteran neural network
inferredcites →https://doi.org/10.1007/bf01933964openalex-snapshot
Muscular and nervous systems of the cubopolyp (Cnidaria)
inferredcites →https://doi.org/10.1038/232582a0openalex-snapshot
Life Cycle of Tripedalia cystophora Conant (Cubomedusae)
inferredcites →https://doi.org/10.1038/281141a0openalex-snapshot
Swimming control in a cubomedusan jellyfish
inferredcites →https://doi.org/10.1085/jgp.52.3.600openalex-snapshot
Epithelial Conduction in Hydromedusae
inferredcites →https://doi.org/10.1093/icb/12.1.35openalex-snapshot
Epidermal Melanin Units Melanocyte-Keratinocyte Interactions
inferredcites →https://doi.org/10.1093/icb/5.3.465openalex-snapshot
PACEMAKERS AND ACTIVITY PATTERNS IN MEDUSAE: HOMAGE TO ROMANES
inferredcites →https://doi.org/10.1098/rspl.1875.0016openalex-snapshot
III. Preliminary observations on the locomotor system of medusæ
inferredcites →https://doi.org/10.1098/rstl.1876.0011openalex-snapshot
XI. The Croonian lecture.--Preliminary observations on the locomotor system of medusæ
inferredcites →https://doi.org/10.1098/rstl.1877.0018openalex-snapshot
XVIII. Further observations on the locomotor system of medusœ
inferredcites →https://doi.org/10.1098/rstl.1878.0017openalex-snapshot
XVII. Observations on the nervous system of Aurelia aurita
inferredcites →https://doi.org/10.1126/science.17918openalex-snapshot
Electrically Coupled, Photosensitive Neurons Control Swimming in a Jellyfish
inferredcites →https://doi.org/10.1242/jcs.s3-95.29.85openalex-snapshot
Observations on the Nerve Fibres of Aurellia aurita
inferredcites →https://doi.org/10.1242/jcs.s3-97.37.59openalex-snapshot
The Nervous System of the Ephyra Larva of Aurellia aurita
inferredcites →https://doi.org/10.1242/jeb.31.4.594openalex-snapshot
The Nerves and Muscles of Medusae
inferredcites →https://doi.org/10.1242/jeb.36.1.72openalex-snapshot
The Nerves and Muscles of Medusae
inferredcites →https://doi.org/10.1242/jeb.51.2.377openalex-snapshot
Two Slow Conduction Systems in the Sea Anemone Calliactis Parasitica
inferredcites →https://doi.org/10.1242/jeb.62.2.421openalex-snapshot
The transmission of impulses in the ectodermal slow conduction system of the sea anemone Calliactis parasitica (Couch)
inferredcites →https://doi.org/10.15083/00037703openalex-snapshot
Notes on the Physiology of Charybdea rastonii
inferredcites →https://doi.org/10.2307/1540493openalex-snapshot
BEHAVIOR AND ELECTRICAL ACTIVITY IN THE HYDROZOAN PROBOSCIDACTYLA FLAVICIRRATA (BRANDT). II. THE MEDUSA
inferredcites →https://doi.org/10.2307/1540562openalex-snapshot
THE ONTOGENY OF SWIMMING BEHAVIOR IN THE SCYPHOZOAN,AURELIA AURITA.I. ELECTROPHYSIOLOGICAL ANALYSIS
inferredcites →https://doi.org/10.2307/1540635openalex-snapshot
ELECTRICAL ACTIVITIES OF THE ANTHOMEDUSAN,SPIROCODON SALTATRIX(TILESIUS)
inferredcites →https://doi.org/10.5134/175745openalex-snapshot
REPORT ON GIANT NERVE FIBRES IN NANOMIA
inferredcites →https://doi.org/10.5134/175754openalex-snapshot
BEHAVIORAL CONTROL SYSTEMS IN MEDUSAE; A COMPARISON BETWEEN HYDRO- AND SCYPHOMEDUSAE
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.4543.4.3zenodo-depositor-declared
Revision of the genus Carybdea (Cnidaria: Cubozoa: Carybdeidae): clarifying the identity of its type species Carybdea marsupialis
inferred← citeshttps://doi.org/10.1002/cne.20658openalex-snapshot
Bilateral symmetric organization of neural elements in the visual system of a coelenterate, Tripedalia cystophora (Cubozoa)
inferred← citeshttps://doi.org/10.1002/cne.25133openalex-snapshot
Neuropeptide expression in the box jellyfish Tripedalia cystophora —New insights into the complexity of a “simple” nervous system
inferred← citeshttps://doi.org/10.1002/j.2040-4603.1996.tb01736.xopenalex-snapshot
Invertebrate Nervous Systems
inferred← citeshttps://doi.org/10.1002/jmor.10472openalex-snapshot
Bilaterally symmetrical rhopalial nervous system of the box jellyfish Tripedalia cystophora
inferred← citeshttps://doi.org/10.1002/neu.480200513openalex-snapshot
The importance of cnidarian synapses for neurobiology
inferred← citeshttps://doi.org/10.1002/syn.890020605openalex-snapshot
Three‐dimensional structure of bidirectional, excitatory chemical synapses in the jellyfish Cyanea capillata
inferred← citeshttps://doi.org/10.1007/978-1-4020-2762-8_17openalex-snapshot
Photoreceptors of cubozoan jellyfish
inferred← citeshttps://doi.org/10.1007/978-1-4613-1955-9_9openalex-snapshot
Organization of Conducting Systems in “Simple” Invertebrates: Porifera, Cnidaria and Ctenophora
inferred← citeshttps://doi.org/10.1007/978-1-4899-0921-3_7openalex-snapshot
Neurons and Their Peptide Transmitters in Coelenterates
inferred← citeshttps://doi.org/10.1007/978-3-031-23216-9_2openalex-snapshot
Cnidarians: Diversity and Evolution of Cnidarian Visual Systems
inferred← citeshttps://doi.org/10.1007/978-3-0348-9219-3_2openalex-snapshot
The nervous systems of Cnidarians
inferred← citeshttps://doi.org/10.1007/978-3-319-92486-1_27openalex-snapshot
Vision Made Easy: Cubozoans Can Advance Our Understanding of Systems-Level Visual Information Processing
inferred← citeshttps://doi.org/10.1007/978-3-642-60659-5_1openalex-snapshot
Lens crystallins of invertebrates
inferred← citeshttps://doi.org/10.1007/978-94-011-3240-4_78openalex-snapshot
Neuropeptides in coelenterates: a review
inferred← citeshttps://doi.org/10.1007/bf00026513openalex-snapshot
Neuropeptides in coelenterates: a review
inferred← citeshttps://doi.org/10.1007/bf00312135openalex-snapshot
Die Ultrastruktur des neuromuskulären Systems der Medusen von Tripedalia cystophora und Carybdea marsupialis (Coelenterata, Cubozoa)
inferred← citeshttps://doi.org/10.1007/bf00614500openalex-snapshot
The cellular eye lens and crystallins of cubomedusan jellyfish
inferred← citeshttps://doi.org/10.1007/bf00679020openalex-snapshot
The physiology of a coelenterate neuromuscular synapse
inferred← citeshttps://doi.org/10.1007/s00359-008-0336-0openalex-snapshot
Swim pacemakers in box jellyfish are modulated by the visual input
inferred← citeshttps://doi.org/10.1007/s00359-013-0839-1openalex-snapshot
Swim pacemaker response to bath applied neurotransmitters in the cubozoan Tripedalia cystophora
inferred← citeshttps://doi.org/10.1007/s00441-005-0134-8openalex-snapshot
Rhopalia are integrated parts of the central nervous system in box jellyfish
inferred← citeshttps://doi.org/10.1007/s00441-007-0393-7openalex-snapshot
The ring nerve of the box jellyfish Tripedalia cystophora
inferred← citeshttps://doi.org/10.1007/s00441-008-0614-8openalex-snapshot
Immunohistochemical evidence for multiple photosystems in box jellyfish
inferred← citeshttps://doi.org/10.1007/s10750-004-2674-4openalex-snapshot
Photoreceptors of cubozoan jellyfish
inferred← citeshttps://doi.org/10.1007/s10750-012-1345-0openalex-snapshot
Contrast and rate of light intensity decrease control directional swimming in the box jellyfish Tripedalia cystophora (Cnidaria, Cubomedusae)
inferred← citeshttps://doi.org/10.1016/0196-9781(85)90417-6openalex-snapshot
Arg-Phe-amide-like peptides in the primitive nervous systems of coelenterates
inferred← citeshttps://doi.org/10.1016/0301-0082(82)90007-7openalex-snapshot
Recent advances and model systems in coelenterate neurobiology
inferred← citeshttps://doi.org/10.1016/0361-9230(88)90030-5openalex-snapshot
Evolutionary and comparative aspects of nociception
inferred← citeshttps://doi.org/10.1016/0742-8413(83)90139-1openalex-snapshot
Neurotransmitters in coelenterates
inferred← citeshttps://doi.org/10.1016/0742-8413(86)90032-0openalex-snapshot
Cholinergic mechanism in Liriope tetraphylla (Cnidaria, Hydrozoa)
inferred← citeshttps://doi.org/10.1016/0742-8413(88)90015-1openalex-snapshot
Pharmacology of the radial neuromuscular system of Liriope tetraphylla (Hydrozoa, Trachymedusae)
inferred← citeshttps://doi.org/10.1016/b978-0-12-408096-6.00001-8openalex-snapshot
Biology and Ecology of Irukandji Jellyfish (Cnidaria: Cubozoa)
inferred← citeshttps://doi.org/10.1016/j.mehy.2005.08.036openalex-snapshot
Is sleep’s ‘supreme mystery’ unraveling? An evolutionary analysis of sleep encounters no mystery; nor does life’s earliest sleep, recently discovered in jellyfish
inferred← citeshttps://doi.org/10.1016/s0074-7696(08)61345-5openalex-snapshot
Peptides in the Nervous Systems of Cnidarians: Structure, Function, and Biosynthesis
inferred← citeshttps://doi.org/10.1016/s0079-6123(08)61170-xopenalex-snapshot
Chapter 11 The peptidergic nervous system of coelenterates
inferred← citeshttps://doi.org/10.1080/10236249509378935openalex-snapshot
Observations on the anatomy and behaviour of the cubozoanCarybdea rastoniihaacke
inferred← citeshttps://doi.org/10.1080/10635150500433615openalex-snapshot
Medusozoan Phylogeny and Character Evolution Clarified by New Large and Small Subunit rDNA Data and an Assessment of the Utility of Phylogenetic Mixture Models
inferred← citeshttps://doi.org/10.1086/697071openalex-snapshot
Regeneration of the Rhopalium and the Rhopalial Nervous System in the Box Jellyfish Tripedalia cystophora
inferred← citeshttps://doi.org/10.1086/699325openalex-snapshot
Tentacle Musculature in the Cubozoan Jellyfish Carybdea marsupialis
inferred← citeshttps://doi.org/10.1086/bblv217n1p35openalex-snapshot
Ultrastructure of the Retinal Synapses in Cubozoans
inferred← citeshttps://doi.org/10.1086/bblv222n1p35openalex-snapshot
Opposite Patterns of Diurnal Activity in the Box Jellyfish Tripedalia cystophora and Copula sivickisi
inferred← citeshttps://doi.org/10.1086/bblv227n3p274openalex-snapshot
Multiple Conducting Systems in the Cubomedusa Carybdea marsupialis
inferred← citeshttps://doi.org/10.1093/icb/43.4.542openalex-snapshot
Visual Ecology and Functional Morphology of Cubozoa (Cnidaria)
inferred← citeshttps://doi.org/10.1093/icb/icv067openalex-snapshot
Cnidarian Nerve Nets and Neuromuscular Efficiency
inferred← citeshttps://doi.org/10.1098/rspb.2020.2494openalex-snapshot
The most efficient metazoan swimmer creates a ‘virtual wall’ to enhance performance
inferred← citeshttps://doi.org/10.1111/j.1432-1033.1996.00449.xopenalex-snapshot
Lens Crystallins of Invertebrates
inferred← citeshttps://doi.org/10.1111/j.1744-7410.2004.tb00139.xopenalex-snapshot
Cladistic analysis of Medusozoa and cnidarian evolution
inferred← citeshttps://doi.org/10.1139/z02-132openalex-snapshot
Neuronal control of swimming in jellyfish: a comparative story
inferred← citeshttps://doi.org/10.1139/z98-193openalex-snapshot
Microanatomy of the bell rim ofAurelia aurita(Cnidaria: Scyphozoa)
inferred← citeshttps://doi.org/10.1242/dev.103.2.249openalex-snapshot
Morphological, cytochemical and neuropharmacological evidence for the presence of catecholamines in hydrozoan planulae
inferred← citeshttps://doi.org/10.1242/jeb.031559openalex-snapshot
Multiple photoreceptor systems control the swim pacemaker activity in box jellyfish
inferred← citeshttps://doi.org/10.1242/jeb.043687openalex-snapshot
Do jellyfish have central nervous systems?
inferred← citeshttps://doi.org/10.1242/jeb.110.1.69openalex-snapshot
Radial Symmetry and the Organization of Central Neurones in A Hydrozoan Jellyfish
inferred← citeshttps://doi.org/10.1242/jeb.111955openalex-snapshot
Electrogenesis in the lower Metazoa and implications for neuronal integration
inferred← citeshttps://doi.org/10.1242/jeb.204.8.1413openalex-snapshot
Why do cubomedusae have only four swim pacemakers?
inferred← citeshttps://doi.org/10.1242/jeb.233197openalex-snapshot
Cytoskeletal and synaptic polarity of LWamide-like+ ganglion neurons in the sea anemone Nematostella vectensis
inferred← citeshttps://doi.org/10.1371/journal.pone.0027201openalex-snapshot
Setting the Pace: New Insights into Central Pattern Generator Interactions in Box Jellyfish Swimming
inferred← citeshttps://doi.org/10.1679/aohc.52.suppl_265openalex-snapshot
Neurones and neuropeptides in coelenterates.
inferred← citeshttps://doi.org/10.17875/gup2013-697openalex-snapshot
Annals of the History and Philosophy of Biology 16/2011
inferred← citeshttps://doi.org/10.17875/gup2023-697openalex-snapshot
Annals of the History and Philosophy of Biology 16/2011
inferred← citeshttps://doi.org/10.2307/1541341openalex-snapshot
APPARENT ABSENCE OF GAP JUNCTIONS IN TWO CLASSES OF CNIDARIA
inferred← citeshttps://doi.org/10.2307/3593133openalex-snapshot
Muscle Organization of the Cubozoan JellyfishTripedalia cystophoraConant 1897
inferred← citeshttps://doi.org/10.25903/6b6r-bq97openalex-snapshot
Taxonomy and phylogeny of Australian cubozoa
inferred← citeshttps://doi.org/10.3389/fphys.2016.00099openalex-snapshot
Hunting in Bioluminescent Light: Vision in the Nocturnal Box Jellyfish Copula sivickisi
inferred← citeshttps://doi.org/10.3800/pbr.12.129openalex-snapshot
Recognition of the Californian cubozoan population as a new species—Carybdea confusa n. sp. (Cnidaria, Cubozoa, Carybdeida)
inferred← citeshttps://doi.org/10.70675/ffef6377z3968z4ab7zb677z254b4877f6a0openalex-snapshot
Bases cellulaires et moléculaires de la régénération chez la méduse Clytia hemisphaerica
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