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An unusual abbreviated larval life in the estuarine burrowing prawn Callianassa kraussi (Crustacea: Decapoda: Thalassinidea)

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

inferredcites →https://doi.org/10.1038/150474a0openalex-snapshot
Larvæ of Decapod Crustacea
inferredcites →https://doi.org/10.1080/00359195109519889openalex-snapshot
THE ECOLOGY OF SOUTH AFRICAN ESTUARIES
inferredcites →https://doi.org/10.1080/00359195109519891openalex-snapshot
THE ECOLOGY OF SOUTH AFRICAN ESTUARIES
inferredcites →https://doi.org/10.2307/1931020openalex-snapshot
Ecological Observations on Callianassa Major Say at Beaufort, North Carolina
inferredcites →https://doi.org/10.2307/2256924openalex-snapshot
The Ecology of Plants and Animals in the Intertidal Regions of the Zwartkops Estuary, Near Port Elizabeth, South Africa
inferredcites →https://doi.org/10.2307/2420244openalex-snapshot
The Natural History of Callianassa californiensis Dana

What points at this work

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

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Soil Neighbors I: Traces of Other Organisms in Paleosols. Crustaceans and Earthworms
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inferred← citeshttps://doi.org/10.1007/s00227-007-0715-zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00227-009-1168-3openalex-snapshot
A tropical/subtropical biogeographic disjunction in southeastern Africa separates two Evolutionarily Significant Units of an estuarine prawn
inferred← citeshttps://doi.org/10.1007/s002270050030openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s002270050503openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10750-012-1060-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0022-0981(86)90230-3openalex-snapshot
Ontogeny of osmoregulation in the estuarine ghost shrimp Callianassa jamaicense var. louisianensis Schmitt (Decapoda, Thalassinidea)
inferred← citeshttps://doi.org/10.1016/0022-0981(87)90039-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0031-0182(78)90094-9openalex-snapshot
Ophiomorpha: Its morphologic, taxonomic, and environmental significance
inferred← citeshttps://doi.org/10.1016/0272-7714(88)90014-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/0300-9629(86)90058-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.earscirev.2024.104988openalex-snapshot
The ichnogenus Ophiomorpha : Taxonomy and environmental distribution
inferred← citeshttps://doi.org/10.1016/j.ecolind.2025.114450openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jembe.2006.06.024openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jsames.2020.103135openalex-snapshot
Pleistocene Ophiomorpha nodosa from Buenos Aires, Argentina: Paleoenvironmental implications for ghost shrimp trace fossils along South America
inferred← citeshttps://doi.org/10.1016/j.palaeo.2005.07.008openalex-snapshot
Commensal worm traces and possible juvenile thalassinidean burrows associated with Ophiomorpha nodosa, Pleistocene, southern Brazil
inferred← citeshttps://doi.org/10.1016/j.palaeo.2008.04.004openalex-snapshot
Terrestrial crustacean breeding trace fossils from the Cretaceous of Patagonia (Argentina): Palaeobiological and evolutionary significance
inferred← citeshttps://doi.org/10.1016/j.palaeo.2015.02.012openalex-snapshot
Ghost shrimps (Decapoda: Axiidea: Callianassidae) as producers of an Upper Miocene trace fossil association from sublittoral deposits of Lake Pannon (Vienna Basin, Slovakia)
inferred← citeshttps://doi.org/10.1016/j.palaeo.2016.04.018openalex-snapshot
Lepeichnus giberti igen. nov. isp. nov. from the upper Miocene of Lepe (Huelva, SW Spain): Evidence for its origin and development with proposal of a new concept, ichnogeny
inferred← citeshttps://doi.org/10.1016/j.palaeo.2017.03.013openalex-snapshot
Solving a cold case: New occurrences reinforce juvenile callianassids as the Ophiomorpha puerilis tracemakers
inferred← citeshttps://doi.org/10.1016/j.palaeo.2019.05.045openalex-snapshot
Fish hunting trace Osculichnus and the oldest Sinusichnus sinuosus from the Upper Devonian of South China
inferred← citeshttps://doi.org/10.1016/j.palaeo.2020.109964openalex-snapshot
Possible ghost-shrimp burrows from the mid-Holocene of northeastern Buenos Aires, Argentina: Implications for breeding and postlarval settlement behavior
inferred← citeshttps://doi.org/10.1016/s0016-7878(78)80019-4openalex-snapshot
Ophiomorpha: a marine indicator?
inferred← citeshttps://doi.org/10.1017/s0022336000034727openalex-snapshot
A new ichnospecies of Spongeliomorpha from the Pleistocene of Sicily
inferred← citeshttps://doi.org/10.1017/s0025315400031386openalex-snapshot
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inferred← citeshttps://doi.org/10.1017/s0025315400047706openalex-snapshot
A contribution to the biology of the burrowing mud shrimp, Callianassa subterranea (Decapoda: Thalassinidea)
inferred← citeshttps://doi.org/10.1017/s0025315406012902openalex-snapshot
Egg size and clutch size in three species of Nihonotrypaea (Decapoda: Thalassinidea: Callianassidae) from western Kyushu, Japan
inferred← citeshttps://doi.org/10.1017/s0025315410000214openalex-snapshot
Burrow morphology and associated animals of the mud shrimpUpogebia yokoyai(Crustacea: Thalassinidea: Upogebiidae)
inferred← citeshttps://doi.org/10.1023/a:1017506917996openalex-snapshot
Aspects of the population dynamics of Neosarmatium meinerti at Mgazana, a warm temperate mangrove swamp in the East Cape, South Africa, investigated using an indirect method
inferred← citeshttps://doi.org/10.1038/s41598-020-58677-1openalex-snapshot
Water filtration by burrowing sandprawns provides novel insights on endobenthic engineering and solutions for eutrophication
inferred← citeshttps://doi.org/10.1080/00222930210125416openalex-snapshot
Reproductive biology ofLimnoria chilensis: another boring peracarid species with extended parental care
inferred← citeshttps://doi.org/10.1080/00359190509519178openalex-snapshot
A century of Zoology and Entomology at Rhodes University, 1905 to 2005
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ZOOPLANKTON AND SOME ENVIRONMENTAL CONDITIONS IN THE BOT RIVER ESTUARY
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Maintenance of Non-Breeding Populations of the Estuarine Prawn Callianassa Kraussi (Crustacea, Anomura, Thalassinidea)
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Population dynamics of the burrowing ghost shrimpCallianassa filholion an intertidal sandflat in New Zealand (Decapoda: Thalassinidea)
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Reproductive strategy of the ghost shrimpCallichirus major(Crustacea: Axiidea: Callianassidae) from the southwestern Atlantic: sexual maturity of females, fecundity, egg features, and reproductive output
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A peculiar reworking ofOphiomorphashafts in the Miocene Nangang Formation, Taiwan
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Temporal changes in the macrobenthos of sandprawn ( Callichirus kraussi ) beds in Swartvlei Estuary, South Africa
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A review of marine invertebrates used as fishing baits and the implications for national and regional management in the Western Indian Ocean
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Discovery of populations endemic to a marine biogeographical transition zone
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The Biology of Upogebia pusilla (Petagna) (Decapoda, Thalassinidea) I. The Burrows
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The Biology of Upogebia pusilla (PETAGNA) (Decapoda, Thalassinidea)
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Abbreviation of larval development and extension of brood care as key features of the evolution of freshwater Decapoda
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Ethologic and ontogenic significance of the Pliocene trace fossil Sinusichnus sinuosus from the northwestern Mediterranean
inferred← citeshttps://doi.org/10.1111/j.1749-7345.1998.tb00978.xopenalex-snapshot
Impacts of Burrowing Ghost Shrimp, Genus Lepidophthalmus Crustacea: Decapoda: Thalassinidea, on Penaeid Shrimp Culture
inferred← citeshttps://doi.org/10.11606/t.59.2012.tde-20052013-151016openalex-snapshot
Status taxonômico de Callichirus major (Say, 1818) sensu lato (Crustacea, Decapoda, Axiidea, Callianassidae) da costa brasileira: taxonomia, sistemática molecular, biologia populacional e reprodutiva
inferred← citeshttps://doi.org/10.1163/156854096x00493openalex-snapshot
Complete Larval Development of the Edible Mud.Shrimp Upogebia Edulis Ngoc-Ho & Chan, 1992 (Decapoda, Thalassinidea, Upogebiidae) Reared in the Laboratory
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LARVAL DEVELOPMENT OF THE GHOST SHRIMP CALLICHIRUS ISLAGRANDE (DECAPODA: THALASSINIDEA: CALLIANASSIDAE) UNDER LABORATORY CONDITIONS
inferred← citeshttps://doi.org/10.1201/b11009-5openalex-snapshot
Bioengineering effects of burrowing thalassinidean shrimps on marine soft-bottom ecosystems
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Estimating connectivity in marine fish populations
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Trace fossils from the Eocene Lillebælt Clay Formation, Røsnæs, Denmark
inferred← citeshttps://doi.org/10.1651/10-3321.1openalex-snapshot
Plankton-Caught Zoeal Stages and Megalopa of the Lobster Shrimp Axius serratus (Decapoda: Axiidae) from the Bay of Fundy, Canada, With A Summary of Axiidean and Gebiidean Literature on Larval Descriptions
inferred← citeshttps://doi.org/10.2307/1548410openalex-snapshot
Advanced Larval Development of Callianassa Tyrrhena (Decapoda: Thalassinidea) and the Effect of Environmental Factors
inferred← citeshttps://doi.org/10.2307/1549444openalex-snapshot
Comparative Larval Development in Two Species of the Burrowing Ghost Shrimp Genus Lepidophthalmus (Decapoda: Callianassidae)
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Subtidal macrozoobenthic community resilience to change following natural mouth breaching of the temporarily open/closed East Kleinemonde Estuary, South Africa
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inferred← citeshttps://doi.org/10.3354/meps079171openalex-snapshot
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inferred← citeshttps://doi.org/10.3354/meps14312openalex-snapshot
Corridors and barriers to marine connectivity around southern Africa
inferred← citeshttps://doi.org/10.3390/d11040064openalex-snapshot
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inferred← citeshttps://doi.org/10.3800/pbr.17.327openalex-snapshot
Life history characteristics and burrow structure of the mud shrimp (Decapoda: Upogebiidae)
inferred← citeshttps://doi.org/10.4067/s0716-078x2003000200007openalex-snapshot
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inferred← citeshttps://doi.org/10.5772/intechopen.75067openalex-snapshot
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inferred← citeshttps://doi.org/10.5894/rgci435openalex-snapshot
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