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Nemertean, copepod, and amphipod symbionts of the dimorphic ascidian Pyura stolonifera near Melbourne, Australia: specificities to host morphs, and factors affecting prevalences

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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/bf00002992openalex-snapshot
Why do anemonefishes inhabit only some host actinians?
inferredcites →https://doi.org/10.1007/bf00042882openalex-snapshot
Parasites as biological indicators of the population biology, migrations, diet, and phylogenetics of fish
inferredcites →https://doi.org/10.1007/bf01989293openalex-snapshot
Ecology of marine parasites
inferredcites →https://doi.org/10.1016/0007-1935(90)90020-4openalex-snapshot
Parasitology—The biology of animal parasites. 6th edn.
inferredcites →https://doi.org/10.1016/0020-7519(87)90109-3openalex-snapshot
Parasites as indicators of host populations
inferredcites →https://doi.org/10.1016/0020-7519(90)90204-zopenalex-snapshot
Marine parasites: An Australian perspective
inferredcites →https://doi.org/10.1016/0022-0981(76)90060-5openalex-snapshot
Some histochemical observations on digestive and other enzymes of the entozoic hoplonemertean Gononemertes australiensis Gibson, with comments on its possible feeding behaviour
inferredcites →https://doi.org/10.1016/0022-0981(84)90190-4openalex-snapshot
The seasonal reproductive cycle of the nemertean Gononemertes australiensis Gibson in relation to that of its ascidian host, Pyura pachydermatina (Herdman)
inferredcites →https://doi.org/10.1016/0022-0981(84)90191-6openalex-snapshot
The seasonal occurrence of the copepod Pachypygusaustralis Gotto (Notodelphyidae) in its host Pyurapachydermatina (Herdman) Pyuridae: Ascidiacea
inferredcites →https://doi.org/10.1016/0022-0981(90)90133-wopenalex-snapshot
Life cycle and population dynamics of the symbiotic copepod Lichomolgus canui Sars associated with the ascidian Halocynthia pyriformis (Rathke)
inferredcites →https://doi.org/10.1016/0169-4758(91)90128-bopenalex-snapshot
Parasites as biological tags
inferredcites →https://doi.org/10.1016/s0065-2881(08)60292-8openalex-snapshot
The Association of Copepods with Marine Invertebrates
inferredcites →https://doi.org/10.1016/s0065-2881(08)60341-7openalex-snapshot
The Biology of Ascidians
inferredcites →https://doi.org/10.1017/s0025315400030393openalex-snapshot
Seasonality of the Association Between the Ascidian, Molgula Complanata, and the Commensal Copepod, Doropygus pulex
inferredcites →https://doi.org/10.1071/mf9790661openalex-snapshot
The Reproduction of the Entozoic Nemertean Gononemertes australiensis Gibson (Nemertea: Hoplonemertea : Monostylifera)–Gonads, Gametes, Embryonic Development and Larval Development
inferredcites →https://doi.org/10.1079/9780851988450.0000openalex-snapshot
Ecology of Marine Parasites
inferredcites →https://doi.org/10.1080/00445096.1974.11448519openalex-snapshot
An Investigation of Pyura Stolonifera (Tunicata) from the Cape Peninsula
inferredcites →https://doi.org/10.1080/01688170.1988.10510361openalex-snapshot
Environmental Sex Determination in a Crustacean Parasite
inferredcites →https://doi.org/10.1080/02541858.1994.11448350openalex-snapshot
Description ofDoropygus pyurusn.sp. (Copepoda, Notodelphyidae) fromPyura stolonifera(Echinodermata, Ascidiacea) in South Africa
inferredcites →https://doi.org/10.1111/j.1096-3642.1974.tb01647.xopenalex-snapshot
A new species of commensal hoplonemertean from Australia
inferredcites →https://doi.org/10.1111/j.1469-7998.1966.tb03005.xopenalex-snapshot
Seasonal cycles of Notodelphys and Ascidicola, copepod associates with Ascidiella (Ascidiacea)
inferredcites →https://doi.org/10.1515/9789882200968-010openalex-snapshot
9 ECOLOGY OF MARINE PARASITES
inferredcites →https://doi.org/10.2307/1548625openalex-snapshot
Ultrastructure and Presumed Function of the Pleural Dermal Glands in the Atypical Male of the Parasitic Copepod Pachypygus gibber (Crustacea: Notodelphyidae)
inferredcites →https://doi.org/10.2307/1548793openalex-snapshot
Population Biology of Doropygus Pulex and Gunenotophorus Globularis (Copepoda), Symbionts Within the Ascidian Polycarpa Pomaria (Savigny)
inferredcites →https://doi.org/10.2307/2287349openalex-snapshot
Biometry: The Principles and Practice of Statistics in Biological Research (2nd ed.).
inferredcites →https://doi.org/10.2307/2413066openalex-snapshot
Coding Multistate Characters, with Special Reference to the Use of Parasites as Characters of Their Hosts
inferredcites →https://doi.org/10.2307/2529087openalex-snapshot
Biometry. The Principles and Practice of Statistics in Biological Research
inferredcites →https://doi.org/10.2307/3243209openalex-snapshot
Symbiosis. An Introduction to Biological Associations
inferredcites →https://doi.org/10.2307/3281335openalex-snapshot
The Use of Ecological Terms in Parasitology (Report of an Ad Hoc Committee of the American Society of Parasitologists)
inferredcites →https://doi.org/10.2307/3282891openalex-snapshot
Parasitology: The Biology of Animal Parasites
inferredcites →https://doi.org/10.3853/j.0812-7387.13.1991.367openalex-snapshot
The families and genera of marine gammaridean Amphipoda (except marine gammaroids). Part 2
inferredcites →https://doi.org/10.5281/zenodo.16245539openalex-snapshot
South African parasitic Copepoda
inferredcites →https://doi.org/10.5479/si.00810282.103openalex-snapshot
Gammaridean Amphipoda from Australia, Part I
inferredcites →https://doi.org/10.5479/si.00963801.108-3390.463openalex-snapshot
North American Copepods of the Family Notodelphyidae
inferredcites →https://doi.org/10.5962/p.254738openalex-snapshot
Doropygus dakarensis n. sp. Copépode parasite de l'Ascidie Pyura stolonifera (Heller, 1878)
inferredcites →https://doi.org/10.7326/0003-4819-86-4-520_4openalex-snapshot
Parasitology. The Biology of Animal Parasites.

What points at this work

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

inferred← citeshttps://doi.org/10.1080/00222933.2021.1948128zenodo-depositor-declared
A new ascidian-dwelling species of Leucothoe Leach, 1814 (Amphipoda: Leucothoidae) from Ilha Grande Bay, Rio de Janeiro state, Brazil
inferred← citeshttps://doi.org/10.11646/zootaxa.3780.2.6zenodo-depositor-declared
The ascidian-associated mysid Corellamysis eltanina gen.nov., sp.nov. (Mysida, Mysidae, Heteromysinae): a new symbiotic relationship from the Southern Ocean
inferred← citeshttps://doi.org/10.1007/s00227-014-2469-8openalex-snapshot
Host preference of a symbiotic flatworm in relation to the ecology of littoral snails
inferred← citeshttps://doi.org/10.1007/s002270000372openalex-snapshot
Population and reproductive biology of two sibling amphipod species from ascidians and sponges
inferred← citeshttps://doi.org/10.1007/s10530-008-9217-2openalex-snapshot
The solitary ascidian Herdmania momus: native (Red Sea) versus non-indigenous (Mediterranean) populations
inferred← citeshttps://doi.org/10.1007/s12526-018-0928-zopenalex-snapshot
Anthropogenic range extension of Leucothoe eltoni Thomas, 2015 (Crustacea: Amphipoda: Leucothoidae)
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2008.03.003openalex-snapshot
Contamination of marine biogenic habitats and effects upon associated epifauna
inferred← citeshttps://doi.org/10.1016/j.rsma.2024.103942openalex-snapshot
Exploring the association between the arrow crab Stenorhynchus lanceolatus (Brullé, 1837) and the sea anemone Telmatactis cricoides (Duchassaing, 1850) in the Canary Islands
inferred← citeshttps://doi.org/10.1023/a:1013005814145openalex-snapshot
Status of the Nemertea as predators in marine ecosystems
inferred← citeshttps://doi.org/10.1038/s41598-025-18125-4openalex-snapshot
Parasitic Pachypygus gibber poses a silent threat to reproduction and development in Ciona robusta
inferred← citeshttps://doi.org/10.1071/9781486300105.part03openalex-snapshot
The invertebrates
inferred← citeshttps://doi.org/10.1080/002229399300371openalex-snapshot
Host-use and population demographics of the ascidian-dwelling amphipod Leucothoe spinicarpa : indication for extended parental care and advanced social behaviour
inferred← citeshttps://doi.org/10.1080/00785236.1997.10428673openalex-snapshot
Reproductive and electrophoretic evidence for genetic maintenance of dimorphism in the ascidianPyura stoloniferanear Melbourne, Australia
inferred← citeshttps://doi.org/10.1093/jcbiol/ruac060openalex-snapshot
Two new endemic species of leucothoid amphipods (Amphipoda: Leucothoidae) from New Zealand and northeastern Indonesia
inferred← citeshttps://doi.org/10.1111/j.1439-0485.1997.tb00441.xopenalex-snapshot
Dimorphism in the Ascidian Pyura stolonifera Near Melbourne, Australia, and its Evaluation Through Field Transplant Experiments
inferred← citeshttps://doi.org/10.1111/j.1744-7410.2010.00184.xopenalex-snapshot
Characterization of macrofaunal assemblages associated with sponges and tunicates collected off the southeastern United States
inferred← citeshttps://doi.org/10.1134/s0012496611050097openalex-snapshot
Interspecific competition of symbiotic and fouling species of red king crab in the Barents Sea
inferred← citeshttps://doi.org/10.1139/z04-156openalex-snapshot
Ecology and natural history of the protochordates
inferred← citeshttps://doi.org/10.11646/zootaxa.1494.1.1openalex-snapshot
New species and host associations of commensal leucothoid amphipods from coral reefs in Florida and Belize (Crustacea:Amphipoda)
inferred← citeshttps://doi.org/10.11646/zootaxa.2754.1.2openalex-snapshot
A revision of the Pyura stolonifera species complex (Tunicata, Ascidiacea), with a description of a new species from Australia
inferred← citeshttps://doi.org/10.1590/s0104-64972015002312openalex-snapshot
Temporal variation of the gammaridean fauna (Crustacea, Amphipoda) associated with the sponge Mycale angulosa (Porifera, Demospongiae) in southeastern Brazil
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