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The ploys of sex: relationships among the mode of reproduction, body size and habitats of coral-reef brittlestars

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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/bimj.19700120319openalex-snapshot

Sokal, R. R., and I. J. Rohlf: Biometry. W. H. Freeman and Company, San Francisco 1969, XXI + 776 S., 89 Abb., 56 Tab., Preis 126/—

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The Dynamics of the Community Associated with a Marine Scleractinian Coral

inferredcites →https://doi.org/10.1007/bf00345098openalex-snapshot

Effect of habitat complexity on population density and species richness in tropical intertidal predatory gastropod assemblages

inferredcites →https://doi.org/10.1007/bf00385227openalex-snapshot

Spatial and temporal patterns in herbivory on a Caribbean fringing reef: the effects on plant distribution

inferredcites →https://doi.org/10.1007/bf00392016openalex-snapshot

Communication and coexistence in a coral community

inferredcites →https://doi.org/10.1007/bf00393221openalex-snapshot

Divide and broadcast: sexual reproduction in the West Indian brittle star Ophiocomella ophiactoides and its relationship to fissiparity

inferredcites →https://doi.org/10.1007/bf00395789openalex-snapshot

Microhabitat and resource utilization in cryptic rocky intertidal echinoderms at Aldabra Atoll, Seychelles

inferredcites →https://doi.org/10.1007/bf00396901openalex-snapshot

Complexity of coral interactions: Influence of time, location of interaction and epifauna

inferredcites →https://doi.org/10.1007/bf00396981openalex-snapshot

Motile cryptofauna of Tul�ar reef flats

inferredcites →https://doi.org/10.1007/bf00397256openalex-snapshot

Size and structure of echinoderm populations associated with different coexisting coral species at Aldabra Atoll, Seychelles

inferredcites →https://doi.org/10.1007/bf00401391openalex-snapshot

Ecological aspects of ophiuroids from the phytal of S. W. Atlantic Ocean warm waters

inferredcites →https://doi.org/10.1007/bf00406885openalex-snapshot

Community structure of ophiuroids (Echinodermata) from three different habitats on a coral reef in Barbados, West Indies

inferredcites →https://doi.org/10.1007/bf02111102openalex-snapshot

A new mothed of classifying the growth form of corals and its application to a field survey of coral-associated animals in Kabira Cove, Ishigaki Island

inferredcites →https://doi.org/10.1007/bf02395281openalex-snapshot

Algal resistance to herbivory on a Caribbean barrier reef

inferredcites →https://doi.org/10.1016/0022-0981(83)90016-3openalex-snapshot

Asexual reproduction in the west indian brittle star Ophiocomella ophiactoides (H.L. Clark) (Echinodermata: Ophiuroidea)

inferredcites →https://doi.org/10.1016/0022-0981(84)90039-xopenalex-snapshot

Resource limitation and recruitment patterns in a coral reef fish assemblage

inferredcites →https://doi.org/10.1016/0022-0981(84)90048-0openalex-snapshot

An apparent instance of recruitment following sexual reproduction in the fissiparous brittlestar Ophiactissavignyi Muller & Troschel

inferredcites →https://doi.org/10.1016/b978-0-12-395527-2.50010-xopenalex-snapshot

ECHINODERMS OF CORAL REEFS

inferredcites →https://doi.org/10.1071/mf9800163openalex-snapshot

Community structure of the fauna associated with the coral Pocillopora damicornis (L.) on the Great Barrier Reef

inferredcites →https://doi.org/10.1080/10236247509378509openalex-snapshot

General morphology and behaviour of gastrozoids and dactylozoids in two species ofmillepora(milleporina, coelenterata)

inferredcites →https://doi.org/10.1086/283186openalex-snapshot

What Are Dandelions and Aphids?

inferredcites →https://doi.org/10.1093/biomet/29.3-4.350openalex-snapshot

THE SIGNIFICANCE OF THE DIFFERENCE BETWEEN TWO MEANS WHEN THE POPULATION VARIANCES ARE UNEQUAL

inferredcites →https://doi.org/10.1093/biomet/34.1-2.28openalex-snapshot

THE GENERALIZATION OF ‘STUDENT'S’ PROBLEM WHEN SEVERAL DIFFERENT POPULATION VARLANCES ARE INVOLVED

inferredcites →https://doi.org/10.1093/icb/15.3.691openalex-snapshot

Adaptational Significance of the Patterns of Ophiuroid Development

inferredcites →https://doi.org/10.1098/rstb.1969.0021openalex-snapshot

The biomorphology of Solomon Islands shores with a discussion of zoning patterns and ecological terminology

inferredcites →https://doi.org/10.1111/j.1439-0485.1984.tb00304.xopenalex-snapshot

The Association of Ophiothrix lineata and Callyspongia vaginalis: A Brittlestar‐Sponge Cleaning Symbiosis?

inferredcites →https://doi.org/10.1111/j.1469-7998.1975.tb03219.xopenalex-snapshot

Feeding mechanisms and feeding strategies of Atlantic reef corals

inferredcites →https://doi.org/10.1126/science.221.4612.747openalex-snapshot

Isolation of Halimedatrial: Chemical Defense Adaptation in the Calcareous Reef-Building AlgaHalimeda

inferredcites →https://doi.org/10.1126/science.847476openalex-snapshot

Sea Urchin Recruitment Patterns and Implications of Commercial Fishing

inferredcites →https://doi.org/10.2307/1541241openalex-snapshot

DEVELOPMENT AND METAMORPHOSIS OF THE BRITTLE STAROPHIOCOMA PUMILA:EVOLUTIONARY AND ECOLOGICAL IMPLICATIONS

inferredcites →https://doi.org/10.2307/1938950openalex-snapshot

Induced Settlement and Metamorphosis of Sand Dollar (Dendraster Ecentricus) Larvae in Predator‐Free sites: Adult Sand Dollar Beds

inferredcites →https://doi.org/10.3354/meps002243openalex-snapshot

Sea Urchin Recruitment: Effect of Substrate Selection on Juvenile Distribution

inferredcites →https://doi.org/10.3354/meps005255openalex-snapshot

Population Structure, Recruitment and Mortality of Two Sea Urchins (Strongylocentrotus franciscanus and S. purpuratus) in a Kelp Forest

inferredcites →https://doi.org/10.3354/meps013131openalex-snapshot

Community patterns of coral-associated decapods

inferredcites →https://doi.org/10.5281/zenodo.13651009openalex-snapshot

The echinoderms of Aldabra and their habitats

inferredcites →https://doi.org/10.5281/zenodo.16648553openalex-snapshot

The echinoderm fauna of Torres Strait: its composition and its origin

inferredcites →https://doi.org/10.5479/si.01960768.12.9openalex-snapshot

The habitat distribution and community structure of the barrier reef complex at Carrie Bow Cay, Belize

inferredcites →https://doi.org/10.5962/bhl.title.11376openalex-snapshot

Studies of the development and larval forms of echinoderms, by Dr. Th. Mortensen.

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/ece3.10096openalex-snapshot

Opportunistic consumption of coral spawn by the ruby brittle star (Ophioderma rubicundum)

inferred← citeshttps://doi.org/10.1007/978-3-642-20051-9_3openalex-snapshot

Central America Echinoderms: Diversity, Ecology and Future Perspectives

inferred← citeshttps://doi.org/10.1007/978-3-642-20051-9_7openalex-snapshot

Echinoderms from Venezuela: Scientific Recount, Diversity and Distribution

inferred← citeshttps://doi.org/10.1007/bf00302020openalex-snapshot

Distributional patterns of mobile fauna associated with Halimeda on the Tiahura coral-reef complex (Moorea, French Polynesia)

inferred← citeshttps://doi.org/10.1007/bf00334473openalex-snapshot

Hurricane effects on backreef echinoderms of the Caribbean

inferred← citeshttps://doi.org/10.1007/bf00349149openalex-snapshot

Reproduction and population dynamics of the fissiparous brittle star Ophiactis savignyi (Echinodermata: Ophiuroidea)

inferred← citeshttps://doi.org/10.1007/bf00394836openalex-snapshot

Submersible and laboratory observations on Asteroschema tenue, a long-armed euryaline brittle star epizoic on gorgonians

inferred← citeshttps://doi.org/10.1007/bf00399584openalex-snapshot

Nutrition and development of brooded embryos in the brittlestar Amphipholis squamata: do endosymbiotic bacteria play a role?

inferred← citeshttps://doi.org/10.1007/bf01313268openalex-snapshot

Genetic structure of populations of two closely related brittle stars with contrasting sexual and asexual life histories, with observations on the genetic structure of a second asexual species

inferred← citeshttps://doi.org/10.1007/bf01319411openalex-snapshot

Reproduction, development and population biology of the Caribbean ophiuroidOphionereis olivacea, a protandric hermaphrodite that broods its young

inferred← citeshttps://doi.org/10.1007/s00227-003-1066-zopenalex-snapshot

Reproduction of Ophiactis resiliens (Echinodermata: Ophiuroidea) in New South Wales with observations on recruitment

inferred← citeshttps://doi.org/10.1007/s00227-004-1327-5openalex-snapshot

Juvenile?adult relationship in the gregarious ophiuroid Ophiothrix fragilis (Echinodermata): a behavioral and morphological study

inferred← citeshttps://doi.org/10.1007/s00338-021-02185-9openalex-snapshot

The biology and ecology of coral rubble and implications for the future of coral reefs

inferred← citeshttps://doi.org/10.1007/s00338-021-02214-7openalex-snapshot

Cryptofaunal diversity in fringing reef rhodoliths

inferred← citeshttps://doi.org/10.1007/s00338-026-02847-6openalex-snapshot

Cryptic coral reef microhabitats and the functional role of brittle stars in biogenic sediment generation

inferred← citeshttps://doi.org/10.1007/s10152-009-0161-zopenalex-snapshot

Brooding in Psolus patagonicus (Echinodermata: Holothuroidea) from Argentina, SW Atlantic Ocean

inferred← citeshttps://doi.org/10.1007/s10530-022-02815-5openalex-snapshot

The effects of the nonnative brittle star Ophiothela mirabilis Verrill, 1867 on the feeding performance of an octocoral host in a southwestern Atlantic rocky shore

inferred← citeshttps://doi.org/10.1016/bs.amb.2016.10.001openalex-snapshot

Patterns and Drivers of Egg Pigment Intensity and Colour Diversity in the Ocean

inferred← citeshttps://doi.org/10.1016/j.csr.2023.104925openalex-snapshot

From emblematic to problematic: The case of Astrospartus mediterraneus (Risso, 1826) (Echinodermata: Ophiuroidea) in the artisanal fishing grounds of the Cap de Creus area (NW Mediterranean Sea)

inferred← citeshttps://doi.org/10.1016/j.dsr.2017.08.007openalex-snapshot

New evidence of brooding in the deep-sea brittle star Astrotoma agassizii Lyman, 1876 from a South Western Atlantic Canyon

inferred← citeshttps://doi.org/10.1016/j.ecss.2013.11.006openalex-snapshot

Small-scale spatial distribution and oogenetic synchrony in brittlestars (Echinodermata: Ophiuroidea)

inferred← citeshttps://doi.org/10.1016/j.jembe.2006.10.055openalex-snapshot

Brooding in echinoderms: How can modern experimental techniques add to our historical perspective?

inferred← citeshttps://doi.org/10.1016/j.jembe.2010.07.021openalex-snapshot

Sediment preference and burrowing behaviour in the sympatric brittlestars Ophiura albida Forbes, 1839 and Ophiura ophiura (Linnaeus, 1758) (Ophiuroidea, Echinodermata)

inferred← citeshttps://doi.org/10.1016/j.ympev.2019.04.014openalex-snapshot

Dark offshoot: Phylogenomic data sheds light on the evolutionary history of a new species of cave brittle star

inferred← citeshttps://doi.org/10.1017/s1755267209000840openalex-snapshot

The effect of two common reef organisms on the growth of the common reef coral Acropora formosa

inferred← citeshttps://doi.org/10.1038/s41598-022-08944-0openalex-snapshot

Mitochondrial phylogeny of the brittle star genus Ophioderma

inferred← citeshttps://doi.org/10.1080/10236248809378676openalex-snapshot

Substrate selection by the burrowing brittlestarmicrophiopholis gracillima(Stimpson) (Echinodermata: Ophiuroidea)

inferred← citeshttps://doi.org/10.1086/285492openalex-snapshot

The Evolution of Parental Care in Brooding Spirorbid Polychaetes: The Effect of Scaling Constraints

inferred← citeshttps://doi.org/10.1086/715843openalex-snapshot

The Waiting Stage, Prolonged Residency in Nursery Habitats by Juveniles of the Predatory Sea StarMarthasterias glacialis

inferred← citeshttps://doi.org/10.1086/725864openalex-snapshot

Fertilization Mode Covaries with Body Size

inferred← citeshttps://doi.org/10.1093/icb/30.1.197openalex-snapshot

Why Life Histories Evolve Differently in the Sea

inferred← citeshttps://doi.org/10.1093/icb/icae048openalex-snapshot

Evolution of Maternal Provisioning and Development in the Ophiuroidea: Egg Size, Larval Form, and Parental Care

inferred← citeshttps://doi.org/10.1111/evo.14639openalex-snapshot

Macroevolutionary patterns in marine hermaphroditism

inferred← citeshttps://doi.org/10.1111/j.1744-7410.2000.tb00109.xopenalex-snapshot

Reproduction, spawning, and development of 5 ophiuroids from Australia and New Zealand

inferred← citeshttps://doi.org/10.1111/j.1744-7410.2006.00049.xopenalex-snapshot

Direct development of the brittle star Amphiodia occidentalis (Ophiuroidea, Amphiuridae) from the northeastern Pacific Ocean

inferred← citeshttps://doi.org/10.1111/j.1744-7410.2007.00110.xopenalex-snapshot

Brooding of pelagic‐type larvae in Ophiopeza spinosa: reproduction and development in a tropical ophiodermatid brittlestar

inferred← citeshttps://doi.org/10.1111/maec.12042openalex-snapshot

Temporal variation of ophiuroids associated with the macroalga A mphiroa fragilissima on a S outhwest A tlantic coral reef

inferred← citeshttps://doi.org/10.1139/z00-218openalex-snapshot

Larval and life-cycle patterns in echinoderms

inferred← citeshttps://doi.org/10.13170/depik.9.2.13582openalex-snapshot

Komunitas Echinodermata di kawasan intertidal Pantai Mandalika Pulau Lombok, Indonesia

inferred← citeshttps://doi.org/10.15517/rbt.v56i3.27022openalex-snapshot

Equinodermos (Echinodermata) del occidente del Archipiélago Sabana-Camagüey, Cuba

inferred← citeshttps://doi.org/10.1590/s1984-46702009000100018openalex-snapshot

Gametogenic cycle of Ophioderma januarii, a common Ophiodermatidae (Echinodermata: Ophiuroidea) in southeastern Brazil

inferred← citeshttps://doi.org/10.1651/09-3187.1openalex-snapshot

Larval Biology of Thaumatopsyllid Copepods Endoparasitic in Caribbean Ophiuroids

inferred← citeshttps://doi.org/10.22458/urj.v13i2.3535openalex-snapshot

Echinoderm research perspectives: A Central American bibliometric review

inferred← citeshttps://doi.org/10.22541/au.167712142.23100333/v1openalex-snapshot

Capricious commensalisms: Consumption of coral spawn by the ruby brittle star ( Ophioderma rubicundum )

inferred← citeshttps://doi.org/10.22541/au.167712142.23100333/v2openalex-snapshot

Capricious commensalisms: Consumption of coral spawn by the ruby brittle star ( Ophioderma rubicundum )

inferred← citeshttps://doi.org/10.2307/1541755openalex-snapshot

Ophiuroid Skeleton Ontogeny Reveals Homologies Among Skeletal Plates of Adults: A Study of Amphiura filiformis, Amphiura stimpsonii and Ophiophragmus filograneus (Echinodermata)

inferred← citeshttps://doi.org/10.2307/1548743openalex-snapshot

Contributions to the Ecology of Paranebalia belizensis from the Waters off Central Belize, Central America

inferred← citeshttps://doi.org/10.2307/3227060openalex-snapshot

Babysitting Brittle Stars: Heterospecific Symbiosis between Ophiuroids (Echinodermata)

inferred← citeshttps://doi.org/10.3390/d16120753openalex-snapshot

Mesophotic and Bathyal Echinoderms of the Italian Seas

inferred← citeshttps://doi.org/10.3897/zookeys.307.4673openalex-snapshot

A taxonomic guide to the brittle-stars (Echinodermata, Ophiuroidea) from the State of Paraíba continental shelf, Northeastern Brazil

inferred← citeshttps://doi.org/10.3897/zookeys.406.6306openalex-snapshot

Ophiuroidea (Echinodermata) from coral reefs in the Mexican Pacific

inferred← citeshttps://doi.org/10.47749/t/unicamp.2008.417231openalex-snapshot

Ecologia de ofiuroides associados a microhabitats biologicos

inferred← citeshttps://doi.org/10.5281/zenodo.16342604openalex-snapshot

The Ecological Significance of Sexual Reproduction by Tropical Green Algae

inferred← citeshttps://doi.org/10.5281/zenodo.16551288openalex-snapshot

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inferred← citeshttps://doi.org/10.71161/ivb.144.4.2025.00035openalex-snapshot

Brittle stars in the plankton: Descriptions of larvae and developing juveniles of the northeastern Pacific Ocean, with a key for their identification

inferred← citeshttps://doi.org/10.7287/peerj.15655v0.1/reviews/1openalex-snapshot

Peer Review #1 of "Integrative species delimitation in the common ophiuroid Ophiothrix angulata (Echinodermata: Ophiuroidea): insights from COI, ITS2, arm coloration, and geometric morphometrics (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.15655v0.1/reviews/2openalex-snapshot

Peer Review #2 of "Integrative species delimitation in the common ophiuroid Ophiothrix angulata (Echinodermata: Ophiuroidea): insights from COI, ITS2, arm coloration, and geometric morphometrics (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.15655v0.1/reviews/3openalex-snapshot

Peer Review #3 of "Integrative species delimitation in the common ophiuroid Ophiothrix angulata (Echinodermata: Ophiuroidea): insights from COI, ITS2, arm coloration, and geometric morphometrics (v0.1)"

inferred← citeshttps://doi.org/10.7287/peerj.15655v0.2/reviews/1openalex-snapshot

inferred← citeshttps://doi.org/10.7287/peerj.15655v0.2/reviews/2openalex-snapshot

inferred← citeshttps://doi.org/10.7287/peerj.15655v0.2/reviews/3openalex-snapshot

inferred← citeshttps://doi.org/10.7717/peerj.15655openalex-snapshot

Integrative species delimitation in the common ophiuroid Ophiothrix angulata (Echinodermata: Ophiuroidea): insights from COI, ITS2, arm coloration, and geometric morphometrics

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