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Born to lose. I. Measures of tissue loss and regeneration by the brittlestar Microphiopholis gracillima (Echinodermata: Ophiuroidea)
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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/bf00312273openalex-snapshot
Morphology and histology of the disc autotomy plane in Ophiophragmus filograneus (Echinodermata, Ophiurida)
inferredcites →https://doi.org/10.1007/bf00334473openalex-snapshot
Hurricane effects on backreef echinoderms of the Caribbean
inferredcites →https://doi.org/10.1007/bf00391963openalex-snapshot
Siphon size and burying depth in deposit- and suspension-feeding benthic bivalves
inferredcites →https://doi.org/10.1007/bf00393108openalex-snapshot
Comparative study of the structure of some tropical and temperate marine soft-bottom macrobenthic communities
inferredcites →https://doi.org/10.1007/bf00394276openalex-snapshot
Field survey of the occurrence and significance of regeneration in Amphiura filiformis (Echinodermata: Ophiuroidea) from Galway Bay, west coast of Ireland
inferredcites →https://doi.org/10.1007/bf00406013openalex-snapshot
Long-term assessment of the population dynamics of Amphiura filiformis (Echinodermata: Ophiuroidea) in Galway Bay (west coast of Ireland)
inferredcites →https://doi.org/10.1007/bf00569441openalex-snapshot
Effects of salinity and calcium concentration on arm regeneration byOphiothrix angulata (Echinodermata: Ophiuroidea)
inferredcites →https://doi.org/10.1007/bf01319415openalex-snapshot
Skeletal changes in the test and jaws of the sea urchinDiadema antillarum in response to food limitation
inferredcites →https://doi.org/10.1007/bf01633006openalex-snapshot
Skeleton resorption in echinoderms: Regression of pedicellarial stalks inSphaerechinus granularis (Echinoida)
inferredcites →https://doi.org/10.1007/bf01986353openalex-snapshot
Effects of disc and arm loss on regeneration byMicrophiopholis gracillima (Echinodermata: Ophiuroidea) in nutrient-free seawater
inferredcites →https://doi.org/10.1016/0022-0981(71)90006-2openalex-snapshot
Studies on Tellina tenuis Da Costa. III. Aspects of general biology and energy flow
inferredcites →https://doi.org/10.1016/0022-0981(75)90014-3openalex-snapshot
The behaviour of some amphiur1d Brittle-Stars
inferredcites →https://doi.org/10.1016/0022-0981(82)90182-4openalex-snapshot
Siphon nipping: Its importance to small fishes and its impact on growth of the bivalve Protothaca staminea (Conrad)
inferredcites →https://doi.org/10.1016/0022-0981(84)90227-2openalex-snapshot
Particle selection by the burrowing brittlestar Micropholis gracillima (Stimpson) (Echinodermata:Ophiuroidea)
inferredcites →https://doi.org/10.1016/0022-0981(85)90094-2openalex-snapshot
Petersen's benthic stations revisited. I. Is the Kattegatt becoming eutrophic?
inferredcites →https://doi.org/10.1016/0022-0981(85)90197-2openalex-snapshot
The effects of sublethal predation on reproduction in the spionid polychaete Polydora ligni Webster
inferredcites →https://doi.org/10.1016/0022-0981(86)90125-5openalex-snapshot
Allocation of nutrient resources to body components by regenerating Luidia clathrata (Say) (Echinodermata: Asteroidea)
inferredcites →https://doi.org/10.1016/0022-0981(87)90174-2openalex-snapshot
Petersen's benthic stations revisited. II. Is the Oslofjord and eastern Skagerrak enriched?
inferredcites →https://doi.org/10.1016/0022-0981(88)90050-0openalex-snapshot
The benthic ecology of Loch Linnhe and Loch Eil, a sea-loch system on the west coast of Scotland. V. Biology of the dominant soft-bottom epifauna and their interaction with the infauna
inferredcites →https://doi.org/10.1016/0022-0981(92)90122-qopenalex-snapshot
The effects of geography and hurricane disturbance on a tropical predator-prey interaction
inferredcites →https://doi.org/10.1016/0077-7579(79)90012-7openalex-snapshot
Secondary production by tail regeneration in a tidal flat population of lugworms (Arenicola marina), cropped by flatfish
inferredcites →https://doi.org/10.1016/0077-7579(79)90037-1openalex-snapshot
Annual food intake by plaice and flounder in a tidal flat area in the dutch wadden sea, with special reference to consumption of regenerating parts of macrobenthic prey
inferredcites →https://doi.org/10.1016/0077-7579(85)90019-5openalex-snapshot
Secondary production by siphon regeneration in a tidal flat population of Macoma balthica
inferredcites →https://doi.org/10.1016/0077-7579(86)90064-5openalex-snapshot
Observations on the population dynamics of amphiura filiformis (ophiuroidea: echinodermata) in the southern north sea and its exploitation by the dab, Limanda limanda
inferredcites →https://doi.org/10.1017/s0025315400027776openalex-snapshot
A Comparative Study of Some Features of the Biology ofAmphiura FiliformisandAmphiura Chiajei[Ophiuroidea] Considered in Relation to their Distribution
inferredcites →https://doi.org/10.1071/mf9870169openalex-snapshot
Natural diet of the tiger prawns Penaeus esculentus and P. semisulcatus
inferredcites →https://doi.org/10.1080/00785236.1981.10426567openalex-snapshot
Density and growth of juvenileAmphiura filiformis(Ophiuroidea) in the Øresund
inferredcites →https://doi.org/10.1080/00785326.1986.10421999openalex-snapshot
Energy flow through anAmphiura filiformis(Ophiuroidea: Echinodermata) population in Galway Bay, west coast of Ireland: A preliminary investigation
inferredcites →https://doi.org/10.1086/284237openalex-snapshot
Evolution of Regeneration Capabilities
inferredcites →https://doi.org/10.1126/science.157.3788.557openalex-snapshot
Negative Growth and Longevity in the Purple Sea Urchin Strongylocentrotus purpuratus (Stimpson)
inferredcites →https://doi.org/10.1130/mem67v1-p461openalex-snapshot
Chapter 17: Bottom Communities (Sublittoral or Shallow Shelf)
inferredcites →https://doi.org/10.1139/z83-375openalex-snapshot
Rate of arm regeneration and potential causes of arm loss in the feather star Florometra serratissima (Echinodermata: Crinoidea)
inferredcites →https://doi.org/10.1201/9781003077565-124openalex-snapshot
Simultaneous allocation of resources to arm regeneration and to somatic and gonadal production in Luidia clathrata (Say) (Echinodermata: Asteroidea)
inferredcites →https://doi.org/10.1201/9781003077565-3openalex-snapshot
Analysis of characteristics of echinoderms associated with stress and disturbance
inferredcites →https://doi.org/10.1201/9781003078913-41openalex-snapshot
The population dynamics of Amphiura filiformis (O.F.Müller) in Galway Bay, West coast of Ireland
inferredcites →https://doi.org/10.1201/9781003078951-25openalex-snapshot
Fréquence et causes presumées de la régénération brachiale chez Amphipholis squamata (Echinodermata: Ophiuroidea)
inferredcites →https://doi.org/10.1201/9781003079224-46openalex-snapshot
Effect of mechanical stress on the calcification pattern in regular echinoid skeletal plates
inferredcites →https://doi.org/10.1515/botm.1976.19.2.119openalex-snapshot
Interpretations of the 14C Method of Measuring the Total Annual Production of Phytoplankton in a South Carolina Estuary
inferredcites →https://doi.org/10.2307/1350801openalex-snapshot
Composition and Seasonality of Zooplankton of North Inlet, South Carolina
inferredcites →https://doi.org/10.2307/1445906openalex-snapshot
Predation: Direct and Indirect Impacts on Aquatic Communities
inferredcites →https://doi.org/10.2307/1535809openalex-snapshot
A STUDY OF THE RATE OF REGENERATION OF THE ARMS IN THE BRITTLE-STAR, OPHIOGLYPHA LACERTOSA
inferredcites →https://doi.org/10.2307/1541162openalex-snapshot
EFFECTS OF BROWSING PREDATORS: ACTIVITY CHANGES IN INFAUNA FOLLOWING TISSUE LOSS
inferredcites →https://doi.org/10.2307/1542439openalex-snapshot
Nutrient Translocation during Early Disc Regeneration in the Brittlestar Microphiopholis gracillima (Stimpson) (Echinodermata: Ophiuroidea)
inferredcites →https://doi.org/10.2307/1941354openalex-snapshot
Brittlestar Beds: Low‐Predation Anachronisms in the British Isles
inferredcites →https://doi.org/10.2307/20022487openalex-snapshot
Regeneration in the Brittle-Star Ophiocoma Pumila, with Reference to the Influence of the Nervous System
inferredcites →https://doi.org/10.2307/4613openalex-snapshot
Physiological Ecology: An Evolutionary Approach to Resource Use
inferredcites →https://doi.org/10.2312/reports-ifm-bhv.1974.14.3.161openalex-snapshot
Arm-Regeneration bei Amphiura filiformis (Ophiuroidea)
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/10.5281/zenodo.16215900openalex-snapshot
The effect of stress and disturbance on echinoderms
inferredcites →https://doi.org/10.5962/bhl.title.37098openalex-snapshot
Life history patterns of three estuarine brittlestars (ophiuroidea) at Cedar Key, Florida
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.4405.1.1zenodo-depositor-declared
Shallow-water brittle stars (Echinodermata: Ophiuroidea) from Araçá Bay (Southeastern Brazil), with spatial distribution considerations
inferred← citeshttps://doi.org/10.1002/jemt.1185openalex-snapshot
Autotomy as a prelude to regeneration in echinoderms
inferred← citeshttps://doi.org/10.1007/bf00119050openalex-snapshot
Sublethal effects of cadmium on arm regeneration in the burrowing brittlestar, Microphiopholis gracillima
inferred← citeshttps://doi.org/10.1007/bf00349232openalex-snapshot
Sublethal predation on Polydora cornuta (Polychaeta: Spionidae): patterns of tissue loss in a field population, predator functional response and potential demographic impacts
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1007/bf00363917openalex-snapshot
Large-scale estimate of somatic growth in Amphiura filiformis (Echinodermata: Ophiuroidea)
inferred← citeshttps://doi.org/10.1007/s00227-006-0274-8openalex-snapshot
Effects of simulated sublethal predation on the growth and regeneration rates of a spionid polychaete in laboratory flumes
inferred← citeshttps://doi.org/10.1007/s00227-006-0431-0openalex-snapshot
Anterior regeneration in the spionid polychaetes Dipolydora quadrilobata and Pygospio elegans
inferred← citeshttps://doi.org/10.1007/s00227-007-0690-4openalex-snapshot
Frequency of sublethal injury in a deepwater ophiuroid, Ophiacantha bidentata, an important component of western Atlantic Lophelia reef communities
inferred← citeshttps://doi.org/10.1007/s00227-012-1884-yopenalex-snapshot
In situ rates of body growth and palp regeneration of a spionid polychaete following simulated sublethal predation
inferred← citeshttps://doi.org/10.1007/s00227-013-2302-9openalex-snapshot
Ephemeral injuries, regeneration frequencies, and intensity of the injury-producing process
inferred← citeshttps://doi.org/10.1007/s00227-016-2854-6openalex-snapshot
Quantitative regeneration in bivalve siphons: difference between short- and long-siphoned species
inferred← citeshttps://doi.org/10.1007/s00227-025-04739-9openalex-snapshot
Low salinities impair heat tolerance and alter reproductive traits with no implications for survival in a marine annelid from coastal habitats
inferred← citeshttps://doi.org/10.1007/s00427-005-0487-8openalex-snapshot
Afuni, a novel transforming growth factor-β gene is involved in arm regeneration by the brittle star Amphiura filiformis
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/10.1016/0022-0981(95)00125-5openalex-snapshot
Quantifying sediment disturbance by browsed spionid polychaetes: implications for competitive and adult-larval interactions
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.jembe.2006.03.003openalex-snapshot
Regeneration of lost siphon tissues in the tellinacean bivalve Nuttallia olivacea
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.jprot.2014.08.011openalex-snapshot
Transcriptomic and proteomic analyses of Amphiura filiformis arm tissue-undergoing regeneration
inferred← citeshttps://doi.org/10.1016/j.marenvres.2007.02.005openalex-snapshot
Effects of sediment organic matter quality on bioaccumulation, degradation, and distribution of pyrene in two macrofaunal species and their surrounding sediment
inferred← citeshttps://doi.org/10.1016/j.seares.2021.102021openalex-snapshot
Sampling nearshore Infaunal ‘weeds’ rather than ‘trees’: Does this orthodoxy undervalue importance of sedimentary biomes?
inferred← citeshttps://doi.org/10.1016/j.ygcen.2019.113220openalex-snapshot
Endocrine regulation of regeneration: Linking global signals to local processes
inferred← citeshttps://doi.org/10.1016/s0022-0981(02)00208-3openalex-snapshot
The effect of salinity on respiration, excretion, regeneration and production in Ophiophragmus filograneus (Echinodermata: Ophiuroidea)
inferred← citeshttps://doi.org/10.1016/s0022-0981(99)00024-6openalex-snapshot
Energy content of Ophiocoma echinata (Echinodermata: Ophiuroidea) maintained at different feeding levels during arm regeneration
inferred← citeshttps://doi.org/10.1016/s1385-1101(96)90762-5openalex-snapshot
Arm regeneration frequency in eight species of ophiuroidea (Echinodermata) from European sea areas
inferred← citeshttps://doi.org/10.1080/00785326.1998.10409380openalex-snapshot
Escape responses in four epibenthic brittle stars (Ophiuroidea: Echinodermata)
inferred← citeshttps://doi.org/10.1080/10236240109379070openalex-snapshot
An escape response behaviour in the brittle star ophiopteris papillosa (echinodermata: Ophiuroidea)
inferred← citeshttps://doi.org/10.1080/17451000.2012.707323openalex-snapshot
The effect of temperature on the inhalant siphon regeneration ofAmiantis purpurata(Lamarck, 1818) (Bivalvia; Veneridae)
inferred← citeshttps://doi.org/10.1080/17451000.2014.904884openalex-snapshot
Effects of temperature and salinity on mortality and metabolism of Ophiopholis mirabilis
inferred← citeshttps://doi.org/10.1086/285947openalex-snapshot
Modeling Interactions of Browsing Predation, Infaunal Activity, and Recruitment in Marine Soft-Sediment Habitats
inferred← citeshttps://doi.org/10.1086/bblv217n3p242openalex-snapshot
Sublethal Predation and Regeneration in Two Onuphid Polychaetes: Patterns and Implications
inferred← citeshttps://doi.org/10.1093/icb/icq099openalex-snapshot
Frequency of Injury and the Ecology of Regeneration in Marine Benthic Invertebrates
inferred← citeshttps://doi.org/10.1111/j.1744-7410.2003.tb00082.xopenalex-snapshot
Effects of variable water motion on regeneration of Hemipholis elongata (Echinodermata, Ophiuroidea)
inferred← citeshttps://doi.org/10.1111/j.1744-7410.2007.00114.xopenalex-snapshot
Morphology of anterior regeneration in two spionid polychaete species: implications for feeding efficiency
inferred← citeshttps://doi.org/10.1139/cjz-79-7-1171openalex-snapshot
Regeneration neurohormones and growth factors in echinoderms
inferred← citeshttps://doi.org/10.1242/jeb.02445openalex-snapshot
Growth or differentiation? Adaptive regeneration in the brittlestarAmphiura filiformis
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.250750openalex-snapshot
Regeneration physiology of invertebrates
inferred← citeshttps://doi.org/10.13102/scb8105openalex-snapshot
Crescimento de Ophioderma cinereum (Müller & Troschel, 1842) (Echinodermata: Ophiuroidea) em duas praias rochosas da cidade de Salvador, Bahia, Brasil
inferred← citeshttps://doi.org/10.1590/s0073-47212010000200006openalex-snapshot
Ophionereis reticulata (Echinodermata, Ophiuroidea)
inferred← citeshttps://doi.org/10.3354/ab00004openalex-snapshot
Delayed arm regeneration in the Antarctic brittle star Ophionotus victoriae
inferred← citeshttps://doi.org/10.3354/ab00435openalex-snapshot
Slow arm regeneration in the Antarctic brittle star Ophiura crassa (Echinodermata, Ophiuroidea)
inferred← citeshttps://doi.org/10.3354/meps247093openalex-snapshot
Utilization of algal and bacterial extracellular polymeric secretions (EPS) by the deposit-feeding brittlestar Amphipholis gracillima (Echinodermata)
inferred← citeshttps://doi.org/10.47749/t/unicamp.2008.417231openalex-snapshot
Ecologia de ofiuroides associados a microhabitats biologicos
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.70675/ffef6377z3968z4ab7zb677z254b4877f6a0openalex-snapshot
Bases cellulaires et moléculaires de la régénération chez la méduse Clytia hemisphaerica
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