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Delayed arm regeneration in the Antarctic brittle star Ophionotus victoriae

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What this work says

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

inferredcites →https://doi.org/10.1007/978-3-642-59419-9_29openalex-snapshot
Ecophysiology of Antarctic marine ectotherms: limits to life
inferredcites →https://doi.org/10.1007/bf00119050openalex-snapshot
Sublethal effects of cadmium on arm regeneration in the burrowing brittlestar, Microphiopholis gracillima
inferredcites →https://doi.org/10.1007/bf00349374openalex-snapshot
Field survey of the occurrence and significance of regeneration in Amphiura chiajei (Echinodermata: Ophiuroidea) from Killary Habrour, west coast of Ireland
inferredcites →https://doi.org/10.1007/bf00349478openalex-snapshot
Abundance and arm loss of the infaunal brittlestar Ophiophragmus filograneus (Echinodermata: Ophiuroidea), with an experimental determination of regeneration rates in natural and planted seagrass beds
inferredcites →https://doi.org/10.1007/bf00350302openalex-snapshot
Born to lose. I. Measures of tissue loss and regeneration by the brittlestar Microphiopholis gracillima (Echinodermata: Ophiuroidea)
inferredcites →https://doi.org/10.1007/bf00442644openalex-snapshot
Feeding biology of the Antarctic brittle star Ophionotus victoriae (Echinodermata: Ophiuroidea)
inferredcites →https://doi.org/10.1007/s00227-006-0428-8openalex-snapshot
Very slow development in two Antarctic bivalve molluscs, the infaunal clam Laternula elliptica and the scallop Adamussium colbecki
inferredcites →https://doi.org/10.1007/s00300-002-0463-yopenalex-snapshot
Ecology of inshore notothenioid fish from the Danco Coast, Antarctic Peninsula
inferredcites →https://doi.org/10.1007/s00300-006-0236-0openalex-snapshot
The influence of depth, site exposure and season on the intensity of iceberg scouring in nearshore Antarctic waters
inferredcites →https://doi.org/10.1007/s003000050229openalex-snapshot
Semi-quantitative study of macrobenthic fauna in the region of the South Shetland Islands and the Antarctic Peninsula
inferredcites →https://doi.org/10.1007/s003000100308openalex-snapshot
Ecophysiology of Antarctic marine ectotherms: limits to life
inferredcites →https://doi.org/10.1007/s00442-004-1648-6openalex-snapshot
Links between the structure of an Antarctic shallow-water community and ice-scour frequency
inferredcites →https://doi.org/10.1016/0022-0981(94)90170-8openalex-snapshot
Arm regeneration in two populations of Acrocnida brachiata (Montagu) (Echinodermata: Ophiuroidea) in Douarnenez Bay, (Brittany: France): An ecological significance
inferredcites →https://doi.org/10.1016/0022-0981(95)00177-8openalex-snapshot
Sub-lethal predation and rate of regeneration in the euryalinid snake star Astrobrachion constrictum (Echinodermata, Ophiuroidea) in a New Zealand fiord
inferredcites →https://doi.org/10.1016/s1385-1101(96)90762-5openalex-snapshot
Arm regeneration frequency in eight species of ophiuroidea (Echinodermata) from European sea areas
inferredcites →https://doi.org/10.1017/s0025315400044891openalex-snapshot
Determination of Growth and Age of Slow Growing Brittle Stars (Echinodermata: Ophiuroidea) From Natural Growth Bands
inferredcites →https://doi.org/10.1038/nrg1923-c1openalex-snapshot
Bridging the regeneration gap: insights from echinoderm models
inferredcites →https://doi.org/10.1093/icb/31.1.65openalex-snapshot
Reproduction of Antarctic Benthic Marine Invertebrates: Tempos, Modes, and Timing
inferredcites →https://doi.org/10.1111/j.0269-8463.2004.00903.xopenalex-snapshot
Extreme sensitivity of biological function to temperature in Antarctic marine species
inferredcites →https://doi.org/10.1111/j.1744-7410.2003.tb00082.xopenalex-snapshot
Effects of variable water motion on regeneration of Hemipholis elongata (Echinodermata, Ophiuroidea)
inferredcites →https://doi.org/10.1242/jeb.02445openalex-snapshot
Growth or differentiation? Adaptive regeneration in the brittlestarAmphiura filiformis
inferredcites →https://doi.org/10.2307/2528285openalex-snapshot
A Simple Method of Resolution of a Distribution into Gaussian Components
inferredcites →https://doi.org/10.3354/meps074091openalex-snapshot
Predation, physical disturbance, and sublethal arm damage in ophiuroids: a Jurassic-Recent comparison
inferredcites →https://doi.org/10.3354/meps111191openalex-snapshot
Trophic biology of antarctic shallow-water echinoderms
inferredcites →https://doi.org/10.3354/meps186001openalex-snapshot
Community recovery following catastrophic iceberg impacts in a soft-sediment shallow-water site at Signy Island, Antarctica
inferredcites →https://doi.org/10.3354/meps219159openalex-snapshot
Seasonality of respiration and ammonium excretion in the Antarctic echinoid Sterechinus neumayeri
inferredcites →https://doi.org/10.3354/meps278141openalex-snapshot
Long-term interannual cycles of the gametogenic ecology of the Antarctic brittle star Ophionotus victoriae
inferredcites →https://doi.org/10.3354/meps318213openalex-snapshot
Metabolism and development of pelagic larvae of Antarctic gastropods with mixed reproductive strategies
inferredcites →https://doi.org/10.5281/zenodo.16215900openalex-snapshot
The effect of stress and disturbance on echinoderms
inferredcites →https://doi.org/10.60950/bgtl.2006.5.chinn.sopenalex-snapshot
Habitat distribution and comparison of brittle star (Echinodermata: Ophiuroidea) arm regeneration on Moorea, French Polynesia

What points at this work

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

inferred← citeshttps://doi.org/10.3897/subtbiol.51.152663zenodo-depositor-declared
Amphicutis stygobita (Echinodermata, Ophiuroidea, Echinodermata, Amphilepididae), a brooding brittle star from anchialine caves in The Bahamas: feeding, reproduction, morphology, paedomorphisms and troglomorphisms
inferred← citeshttps://doi.org/10.1002/jmor.21296openalex-snapshot
Morphogenesis and histogenesis during the arm regeneration in a basket star Astrocladus dofleini (Euryalida, Ophiuroidea, Echinodermata)
inferred← citeshttps://doi.org/10.1007/978-1-0716-2172-1_1openalex-snapshot
The Hazards of Regeneration: From Morgan’s Legacy to Evo-Devo
inferred← citeshttps://doi.org/10.1007/978-3-031-51282-7_26openalex-snapshot
Extreme Biomimetik
inferred← citeshttps://doi.org/10.1007/978-3-319-45340-8_1openalex-snapshot
Psychrophiles as Sources for Bioinspiration in Biomineralization and Biological Materials Science
inferred← citeshttps://doi.org/10.1007/978-3-319-92483-0_26openalex-snapshot
Extreme Biomimetics
inferred← citeshttps://doi.org/10.1007/978-3-319-92486-1_14openalex-snapshot
Regeneration in Stellate Echinoderms: Crinoidea, Asteroidea and Ophiuroidea
inferred← citeshttps://doi.org/10.1007/s00435-009-0095-7openalex-snapshot
Wound healing and arm regeneration in Ophioderma longicaudum and Amphiura filiformis (Ophiuroidea, Echinodermata): comparative morphogenesis and histogenesis
inferred← citeshttps://doi.org/10.1016/j.aquatox.2011.03.001openalex-snapshot
Immune suppression of the echinoderm Asterias rubens (L.) following long-term ocean acidification
inferred← citeshttps://doi.org/10.1016/j.crvi.2013.10.004openalex-snapshot
Thermotolerance and regeneration in the brittle star species complex Ophioderma longicauda: A preliminary study comparing lineages and Mediterranean basins
inferred← citeshttps://doi.org/10.1016/j.jembe.2011.06.032openalex-snapshot
Dynamic gene expression profiles during arm regeneration in the brittle star Amphiura filiformis
inferred← citeshttps://doi.org/10.1016/j.jembe.2011.12.001openalex-snapshot
Gene expression and regeneration in ophiuroids: A study of transcriptional activity and regeneration in the temperate Amphiura filiformis and Antarctic Ophionotus victoriae
inferred← citeshttps://doi.org/10.1016/j.jembe.2017.05.012openalex-snapshot
Effects of CO2, pH and temperature on respiration and regeneration in the burrowing brittle stars Hemipholis cordifera and Microphiopholis gracillima
inferred← citeshttps://doi.org/10.1016/j.margen.2012.05.003openalex-snapshot
Transcriptome pyrosequencing of the Antarctic brittle star Ophionotus victoriae
inferred← citeshttps://doi.org/10.1016/j.susmat.2022.e00447openalex-snapshot
The philosophy of extreme biomimetics
inferred← citeshttps://doi.org/10.1016/j.tree.2009.08.005openalex-snapshot
Evolution of animal regeneration: re-emergence of a field
inferred← citeshttps://doi.org/10.1016/j.tree.2015.09.014openalex-snapshot
A Cold Limit to Adaptation in the Sea
inferred← citeshttps://doi.org/10.1017/9781108683319openalex-snapshot
Life in Extreme Environments
inferred← citeshttps://doi.org/10.1017/9781108683319.001openalex-snapshot
Introduction
inferred← citeshttps://doi.org/10.1017/9781108683319.002openalex-snapshot
Extreme environments: responses and adaptation to change
inferred← citeshttps://doi.org/10.1017/9781108683319.003openalex-snapshot
Physiological traits of the Greenland sharkSomniosus microcephalusobtained during the TUNU-Expeditions to Northeast Greenland
inferred← citeshttps://doi.org/10.1017/9781108683319.004openalex-snapshot
Metazoan adaptation to deep-sea hydrothermal vents
inferred← citeshttps://doi.org/10.1017/9781108683319.005openalex-snapshot
Extremophiles populating high-level natural radiation areas (HLNRAs) in Iran
inferred← citeshttps://doi.org/10.1017/9781108683319.006openalex-snapshot
Biodiversity, bioenergetic processes, and biotic and abiotic interactions
inferred← citeshttps://doi.org/10.1017/9781108683319.007openalex-snapshot
Metazoan life in anoxic marine sediments
inferred← citeshttps://doi.org/10.1017/9781108683319.008openalex-snapshot
How to survive winter?
inferred← citeshttps://doi.org/10.1017/9781108683319.009openalex-snapshot
Vertebrate viruses in polar ecosystems
inferred← citeshttps://doi.org/10.1017/9781108683319.010openalex-snapshot
Life in extreme environments and the responses to change: the example of polar environments
inferred← citeshttps://doi.org/10.1017/9781108683319.011openalex-snapshot
Life in the extreme environments of our planet under pressure
inferred← citeshttps://doi.org/10.1017/9781108683319.012openalex-snapshot
The ecophysiology of responding to change in polar marine benthos
inferred← citeshttps://doi.org/10.1017/9781108683319.013openalex-snapshot
The Southern Ocean: an extreme environment or just home of unique ecosystems?
inferred← citeshttps://doi.org/10.1017/9781108683319.014openalex-snapshot
Microorganisms in cryoturbated organic matter of Arctic permafrost soils
inferred← citeshttps://doi.org/10.1017/9781108683319.015openalex-snapshot
Chemical ecology in the Southern Ocean
inferred← citeshttps://doi.org/10.1017/9781108683319.016openalex-snapshot
Metabolic and taxonomic diversity in antarctic subglacial environments
inferred← citeshttps://doi.org/10.1017/9781108683319.017openalex-snapshot
Life and habitability
inferred← citeshttps://doi.org/10.1017/9781108683319.018openalex-snapshot
Analytical astrobiology: the search for life signatures and the remote detection of biomarkers through their Raman spectral interrogation
inferred← citeshttps://doi.org/10.1017/9781108683319.019openalex-snapshot
Adaptation/acclimatisation mechanisms of oxyphototrophic microorganisms and their relevance to astrobiology
inferred← citeshttps://doi.org/10.1017/9781108683319.020openalex-snapshot
Life at the extremes
inferred← citeshttps://doi.org/10.1017/9781108683319.021openalex-snapshot
Index
inferred← citeshttps://doi.org/10.1017/9781108683319.022openalex-snapshot
Plate Section (PDF Only)
inferred← citeshttps://doi.org/10.1038/s41598-024-66151-5openalex-snapshot
Late Holocene echinoderm assemblages can serve as paleoenvironmental tracers in an Antarctic fjord
inferred← citeshttps://doi.org/10.1086/605982openalex-snapshot
Macrophysiology: A Conceptual Reunification
inferred← citeshttps://doi.org/10.1111/j.0906-7590.2008.05456.xopenalex-snapshot
Likely responses of the Antarctic benthos to climate‐related changes in physical disturbance during the 21st century, based primarily on evidence from the West Antarctic Peninsula region
inferred← citeshttps://doi.org/10.1111/j.0906-7590.2008.5456.xopenalex-snapshot
Likely responses of the Antarctic benthos to climate-related changes in physical disturbance during the 21st century, based primarily on evidence from the West Antarctic Peninsula region
inferred← citeshttps://doi.org/10.1111/j.1365-2486.2012.02755.xopenalex-snapshot
Marine invertebrate skeleton size varies with latitude, temperature and carbonate saturation: implications for global change and ocean acidification
inferred← citeshttps://doi.org/10.1186/s13059-025-03542-5openalex-snapshot
Chromosome-level genome assembly and single-cell analysis unveil molecular mechanisms of arm regeneration in the ophiuroid Ophiura sarsii vadicola
inferred← citeshttps://doi.org/10.1242/jeb.242848openalex-snapshot
Plasticity in fluctuating hydrodynamic conditions: tube foot regeneration in sea urchins
inferred← citeshttps://doi.org/10.1242/jeb.244613openalex-snapshot
The added costs of winter ocean warming for metabolism, arm regeneration and survival in the brittle star Ophionereis schayeri
inferred← citeshttps://doi.org/10.1242/jeb.249426openalex-snapshot
Long-term study of the combined effects of ocean acidification and warming on the mottled brittle star, Ophionereis fasciata
inferred← citeshttps://doi.org/10.1371/journal.pone.0133860openalex-snapshot
Tissue Regeneration and Biomineralization in Sea Urchins: Role of Notch Signaling and Presence of Stem Cell Markers
inferred← citeshttps://doi.org/10.1387/ijdb.180031mmopenalex-snapshot
The evolution of regeneration – where does that leave mammals?
inferred← citeshttps://doi.org/10.15252/embr.201643795openalex-snapshot
Animal regeneration: ancestral character or evolutionary novelty?
inferred← citeshttps://doi.org/10.15517/rbt.v63i2.23164openalex-snapshot
Histological analysis after arm tip amputation in the brittle star Ophioplocus januarii (Echinodermata: Ophiuroidea).
inferred← citeshttps://doi.org/10.2110/palo.2012.p12-100ropenalex-snapshot
DISSOLUTION OF OPHIUROID OSSICLES ON THE SHALLOW ANTARCTIC SHELF: IMPLICATIONS FOR THE FOSSIL RECORD AND OCEAN ACIDIFICATION
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4237645/v1openalex-snapshot
Fjords, Echinoderms and the Holocene: a new ecological proxy from the Ross Sea (Edisto Inlet)
inferred← citeshttps://doi.org/10.3354/ab00435openalex-snapshot
Slow arm regeneration in the Antarctic brittle star Ophiura crassa (Echinodermata, Ophiuroidea)
inferred← citeshttps://doi.org/10.3389/fcell.2021.768641openalex-snapshot
Regeneration in Echinoderms: Molecular Advancements
inferred← citeshttps://doi.org/10.3389/fevo.2021.621686openalex-snapshot
Evolution of Regeneration in Animals: A Tangled Story
inferred← citeshttps://doi.org/10.3390/genes15111448openalex-snapshot
Exposure to High Concentrations of Tetrabromobisphenol A Slows the Process of Tissue Regeneration and Induces an Imbalance of Metabolic Homeostasis in the Regenerated Intestines of Apostichopus japonicus
inferred← citeshttps://doi.org/10.70675/6012d53dz2ffaz42b5za1f4z693eb4c703deopenalex-snapshot
Etude écologique et génétique du complexe d'espèces cryptiques Ophioderma longicauda (Ophiuroidea : Echinodermata) : comparaison entre lignées incubantes et lignées produisant des larves planctoniques.
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