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Prudent female allocation by modular hermaphrodites: female investment is promoted by the opportunity to outcross in cyclostome bryozoans

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What this work says

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

inferredcites →https://doi.org/10.1007/978-1-4615-6974-9_6openalex-snapshot
Modification of the Gender of Seed Plants in Varying Conditions
inferredcites →https://doi.org/10.1007/978-1-4899-3043-9openalex-snapshot
Plant Breeding Systems
inferredcites →https://doi.org/10.1007/978-4-431-66982-1_48openalex-snapshot
Laboratory Studies of Mating in the Aplousobranch Diplosoma listerianum
inferredcites →https://doi.org/10.1007/978-94-007-7146-8openalex-snapshot
Evolution of Sexual Reproduction in Marine Invertebrates: Example of gymnolaemate bryozoans
inferredcites →https://doi.org/10.1007/bf01313478openalex-snapshot
Storage of exogenous sperm by the compound ascidianDiplosoma listerianum
inferredcites →https://doi.org/10.1007/s002270100566openalex-snapshot
Inbreeding and hermaphroditism in the sessile-brooding bryozoan Celleporella hyalina
inferredcites →https://doi.org/10.1016/0022-0981(93)90029-nopenalex-snapshot
Effects of diet on life-history parameters of the marine bryozoan, Celleporella hyalina (L.)
inferredcites →https://doi.org/10.1016/0022-5193(77)90363-0openalex-snapshot
Simultaneous hermaphroditism; cost and benefit
inferredcites →https://doi.org/10.1016/b978-012100543-6/50032-5openalex-snapshot
Mating Conflicts and Sperm Competition in Simultaneous Hermaphrodites
inferredcites →https://doi.org/10.1016/s0169-5347(00)89138-7openalex-snapshot
The ‘paradox’ of polyembryony
inferredcites →https://doi.org/10.1038/251556b0openalex-snapshot
Reproduction of marine invertebrates
inferredcites →https://doi.org/10.1038/263125a0openalex-snapshot
Why be an hermaphrodite?
inferredcites →https://doi.org/10.1073/pnas.1334011100openalex-snapshot
Stress promotes maleness in hermaphroditic modular animals
inferredcites →https://doi.org/10.1073/pnas.162339699openalex-snapshot
Female investment is retarded pending reception of allosperm in a hermaphroditic colonial invertebrate
inferredcites →https://doi.org/10.1073/pnas.76.5.2480openalex-snapshot
Simultaneous hermaphroditism and sexual selection
inferredcites →https://doi.org/10.1080/00785326.1972.10430099openalex-snapshot
Fertilization in the Bryozoa
inferredcites →https://doi.org/10.1086/bblv219n1p27openalex-snapshot
Effects of Selfing on Offspring Survival and Reproduction in a Colonial Simultaneous Hermaphrodite (Bugula stolonifera, Bryozoa)
inferredcites →https://doi.org/10.1093/icb/icj037openalex-snapshot
The third way: spermcast mating in sessile marine invertebrates
inferredcites →https://doi.org/10.1098/rspb.1986.0046openalex-snapshot
Life history variation in Celleporella hyalina (Bryozoa)
inferredcites →https://doi.org/10.1098/rspb.1996.0061openalex-snapshot
Female control of paternity in the internally fertilizing compound ascidian Diplosoma listerianum. II. Investigation of male mating success using RAPD markers
inferredcites →https://doi.org/10.1098/rspb.1998.0353openalex-snapshot
Fertilization in the sea: are the hazards of broadcast spawning avoided when free–spawned sperm fertilize retained eggs?
inferredcites →https://doi.org/10.1098/rspb.2000.1124openalex-snapshot
Water–borne sperm trigger vitellogenic egg growth in two sessile marine invertebrates
inferredcites →https://doi.org/10.1098/rspl.1895.0060openalex-snapshot
VI. On the development of Lichenopora verrucaria , Fabr
inferredcites →https://doi.org/10.1111/brv.12189openalex-snapshot
Matrotrophy and placentation in invertebrates: a new paradigm
inferredcites →https://doi.org/10.1111/evo.12039openalex-snapshot
FROM INCIPIENT TO SUBSTANTIAL: EVOLUTION OF PLACENTOTROPHY IN A PHYLUM OF AQUATIC COLONIAL INVERTEBRATES
inferredcites →https://doi.org/10.1111/j.0014-3820.2006.tb00525.xopenalex-snapshot
ANIMALS MIX IT UP TOO: THE DISTRIBUTION OF SELF-FERTILIZATION AMONG HERMAPHRODITIC ANIMALS
inferredcites →https://doi.org/10.1111/j.1095-8312.1930.tb01330.xopenalex-snapshot
Presidential Address, 24th May, 1929.
inferredcites →https://doi.org/10.1111/j.1095-8312.2009.01312.xopenalex-snapshot
Patterns of self compatibility, inbreeding depression, outcrossing, and sex allocation in a marine bryozoan suggest the predominating influence of sperm competition
inferredcites →https://doi.org/10.1111/j.1558-5646.2009.00669.xopenalex-snapshot
TESTS OF SEX ALLOCATION THEORY IN SIMULTANEOUSLY HERMAPHRODITIC ANIMALS
inferredcites →https://doi.org/10.1126/science.1092180openalex-snapshot
Evolutionary Ecology of the Prezygotic Stage
inferredcites →https://doi.org/10.1242/jcs.s2-34.135.199openalex-snapshot
On the Occurrence of Embryonic Fission in Cyclostomatous Polyzoa
inferredcites →https://doi.org/10.1242/jcs.s2-39.153.71openalex-snapshot
On the Development of Lichenopora verrucaria, Fabr
inferredcites →https://doi.org/10.1242/jcs.s2-41.161.73openalex-snapshot
On the Development of Tubulipora, and on some British and Northern Species of this Genus
inferredcites →https://doi.org/10.2307/2402622openalex-snapshot
Population Biology of Plants.
inferredcites →https://doi.org/10.2307/j.ctt2250w9nopenalex-snapshot
Population Biology and Evolution of Clonal Organisms
inferredcites →https://doi.org/10.3354/meps061125openalex-snapshot
Prevalence of cross-fertilization in the hermaphroditic compound ascidian Diplosoma listerianum
inferredcites →https://doi.org/10.3354/meps07850openalex-snapshot
Independent evolution of matrotrophy in the major classes of Bryozoa: transitions among reproductive patterns and their ecological background
inferredcites →https://doi.org/10.3354/meps188073openalex-snapshot
Molecular genetic evidence for the prevalence of outcrossing in the hermaphroditic brooding bryozoan Celleporella hyalina
inferredcites →https://doi.org/10.3354/meps224087openalex-snapshot
Age-dependent loss of fertility in water-borne sperm of the bryozoan Celleporella hyalina
inferredcites →https://doi.org/10.3989/scimar.2005.69s1169openalex-snapshot
Lessons in modularity: the evolutionary ecology of colonial invertebrates
inferredcites →https://doi.org/10.5860/choice.31-3778openalex-snapshot
The Natural history of inbreeding and outbreeding: theoretical and empirical perspectives
inferredcites →https://doi.org/10.5860/choice.49-0248openalex-snapshot
Hermaphroditism: a primer on the biology, ecology, and evolution of dual sexuality
inferredcites →https://doi.org/10.5860/choice.50-1469openalex-snapshot
Animal evolution: interrelationships of the living phyla
inferredcites →https://doi.org/10.5962/bhl.title.104481openalex-snapshot
The effects of cross and self fertilisation in the vegetable kingdom
inferredcites →https://doi.org/10.5962/bhl.title.110800openalex-snapshot
The effects of cross and self fertilisation in the vegetable kingdom /
inferredcites →https://doi.org/10.5962/bhl.title.48714openalex-snapshot
Contribution à l'histoire naturelle des bryozoaires ectoproctes marins
inferredcites →https://doi.org/10.7312/columbia/9780231153867.001.0001openalex-snapshot
Hermaphroditism
inferredcites →https://doi.org/10.7312/steb94536openalex-snapshot
Variation and Evolution in Plants

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.4484.1.1zenodo-depositor-declared
Bryozoa (Cyclostomata and Ctenostomata) from polymetallic nodules in the Russian exploration area, Clarion–Clipperton Fracture Zone, eastern Pacific Ocean—taxon novelty and implications of mining
inferred← citeshttps://doi.org/10.1002/9781118454961.refsopenalex-snapshot
References
inferred← citeshttps://doi.org/10.1007/978-1-0716-2172-1_8openalex-snapshot
Collecting and Culturing Bryozoans for Regenerative Studies
inferred← citeshttps://doi.org/10.1016/b978-0-08-102871-1.00003-8openalex-snapshot
Phylum Bryozoa
inferred← citeshttps://doi.org/10.1017/s0025315419000286openalex-snapshot
Colonies as dynamic systems: reconstructing the life history of Cribrilina annulata (Bryozoa) on two algal substrates
inferred← citeshttps://doi.org/10.1086/743184openalex-snapshot
First Transcriptomic Insights into the Invertebrate Placental Analogue: Differential Gene Expression in Gonozooids of Crisiella producta (Bryozoa, Cyclostomatida)
inferred← citeshttps://doi.org/10.1098/rstb.2015.0541openalex-snapshot
Sexual selection in hermaphrodites, sperm and broadcast spawners, plants and fungi
inferred← citeshttps://doi.org/10.1111/brv.12478openalex-snapshot
Modularity is the mother of invention: a review of polymorphism in bryozoans
inferred← citeshttps://doi.org/10.1186/s12862-021-01775-zopenalex-snapshot
Three in one: evolution of viviparity, coenocytic placenta and polyembryony in cyclostome bryozoans
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