in

Behavioral traits and territoriality in the symbiotic scaleworm Ophthalmonoe pettiboneae

[adace-ad id="91168"]
  • 1.

    Baeza, J. A. & Thiel, M. Predicting territorial behavior in symbiotic crabs using host characteristics: A comparative study and proposal of a model. Mar. Biol. 142, 93–100. https://doi.org/10.1007/s00227-002-0927-1 (2003).

    Article 

    Google Scholar 

  • 2.

    Kamran, M. & Moore, P. A. Dominance and territory. In Encyclopedia of Evolutionary Psychological Science (eds Shackelford, T. K. & Weekes-Shackelford, V. A.) 1–4 (Springer, 2016).

    Google Scholar 

  • 3.

    Grant, J. W. A. Whether or not to defend? The influence of resource distribution. Mar. Behav. Physiol. 22, 137–153. https://doi.org/10.1080/10236249309378862 (1993).

    ADS 
    Article 

    Google Scholar 

  • 4.

    Duffy, J. E. The ecology and evolution of eusociality in sponge-dwelling shrimp. In Genes, Behaviors and Evolution of Social Insects (ed. Kikuchi, T.) 217–254 (Hokkaido University Press, 2002).

    Google Scholar 

  • 5.

    Baeza, J. A., Stotz, W. & Thiel, M. Agonistic behaviour and development of territoriality during ontogeny of the sea anemone dwelling crab Allopetrolisthes spinifrons (H. Milne Edwards, 1837)(Decapoda: Anomura: Porcellanidae). Mar. Freshw. Behav. Physiol. 35, 189–202. https://doi.org/10.1080/1023624021000003817 (2002).

    Article 

    Google Scholar 

  • 6.

    Castro, P. Symbiotic Brachyura. In Treatise on Zoology-Anatomy, Taxonomy, Biology. The Crustacea, Volume 9 Part C Vol. 2 (eds Castro, P. et al.) 543–581 (Brill, 2015).

    Chapter 

    Google Scholar 

  • 7.

    Wilson, E. O. Sociobiology: The New Synthesis (Harvard University, 1975).

    Google Scholar 

  • 8.

    Burt, W. H. Territoriality and home range concepts as applied to mammals. J. Mammal. 24, 346–352. https://doi.org/10.2307/1374834 (1943).

    Article 

    Google Scholar 

  • 9.

    Gerking, S. D. Feeding Ecology of Fish (Academic Press, 2014).

    Google Scholar 

  • 10.

    Barrows, E. M. Animal Behavior Desk Reference: A Dictionary of Animal Behavior, Ecology, and Evolution (CRC Press, 2000).

    Book 

    Google Scholar 

  • 11.

    Hardy, I. C. W. & Briffa, M. Animal Contests Vol. 357 (Cambridge University Press, 2013).

    Book 

    Google Scholar 

  • 12.

    Dimock, R. V. Jr. Intraspecific aggression and the distribution of a symbiotic polychaete on its host. In Symbiosis in the Sea (ed. Vernberg, W. B.) 29–44 (University of South Carolina Press, 1974).

    Google Scholar 

  • 13.

    Duffy, J. E., Morrison, C. L. & Macdonald, K. S. Colony defense and behavioral differentiation in the eusocial shrimp Synalpheus regalis. Behav. Ecol. Sociobiol. 51, 488–495. https://doi.org/10.1007/s00265-002-0455-5 (2002).

    Article 

    Google Scholar 

  • 14.

    Huber, M. E. Aggressive behavior of Trapezia intermedia Miers and T. digitalis Latreille (Brachyura: Xanthidae). J. Crustacean Biol. 7, 238–248. https://doi.org/10.2307/1548604 (1987).

    Article 

    Google Scholar 

  • 15.

    Douglas, A. The Symbiotic Habit (Princeton University Press, 2010).

    Google Scholar 

  • 16.

    Williams, J. D. & McDermott, J. J. Hermit crab biocoenoses: A worldwide review of the diversity and natural history of hermit crab associates. J. Exp. Mar. Biol. Ecol. 305, 1–128. https://doi.org/10.1016/j.jembe.2004.02.020 (2004).

    Article 

    Google Scholar 

  • 17.

    Fautin, D. G. The anemonefish symbiosis: What is known and what is not. Symbiosis 10, 23–46 (1991).

    Google Scholar 

  • 18.

    Martin, D. & Britayev, T. A. Symbiotic polychaetes: Review of known species. Oceanogr. Mar. Biol. Ann. Rev. 36, 217–340 (1998).

    Google Scholar 

  • 19.

    Fernández-Leborans, G. Epibiosis in Crustacea: An overview. Crustaceana 83, 549–640. https://doi.org/10.1163/001121610X532648 (2010).

    Article 

    Google Scholar 

  • 20.

    Stella, J. S., Pratchett, M. S., Hutchings, P. A. & Jones, G. P. Diversity, importance and vulnerability of coral-associated invertebrates. Oceanogr. Mar. Biol. Ann. Rev. 49, 43–116 (2011).

    Google Scholar 

  • 21.

    Thiel, M. & Baeza, J. A. Factors affecting the social behaviour of crustaceans living symbiotically with other marine invertebrates: a modelling approach. Symbiosis 30, 163–190 (2001).

    Google Scholar 

  • 22.

    Jones, K. M. M. The effect of territorial damselfish (family Pomacentridae) on the space use and behaviour of the coral reef fish Halichoeres bivittatus (Bloch, 1791) (family Labridae). J. Exp. Mar. Biol. Ecol. 324, 99–111. https://doi.org/10.1016/j.jembe.2005.04.009 (2005).

    Article 

    Google Scholar 

  • 23.

    Thiel, M., Zander, A. & Baeza, J. A. Movements of the symbiotic crab Liopetrolisthes mitra between its host sea urchin Tetrapygus niger. Bull. Mar. Sci. 72, 89–101 (2003).

    Google Scholar 

  • 24.

    Marin, I. & Britayev, T. A. Symbiotic Community Associated with Corals Galaxea Oken, 1815 (Euphillidae: Scleractinia) Vol. 148 (KMK Press, 2014).

    Google Scholar 

  • 25.

    Ross, R. M. Territorial behavior and ecology of the anemonefish Amphiprion melanopus on Guam. Z. Tierpsychol. 46, 71–83. https://doi.org/10.1111/j.1439-0310.1978.tb01439.x (1978).

    Article 

    Google Scholar 

  • 26.

    Kobayashi, M. & Hattori, A. Spacing pattern and body size composition of the protandrous anemonefish Amphiprion frenatus inhabiting colonial host anemones. Ichthyol. Res. 53, 1–6. https://doi.org/10.1007/s10228-005-0305-3 (2006).

    Article 

    Google Scholar 

  • 27.

    Huebner, L. K., Dailey, B., Titus, B. M., Khalaf, M. & Chadwick, N. E. Host preference and habitat segregation among Red Sea anemonefish: Effects of sea anemone traits and fish life stages. Mar. Ecol. Progr. Ser. 464, 1–15. https://doi.org/10.3354/meps09964 (2012).

    ADS 
    Article 

    Google Scholar 

  • 28.

    Duffy, J. E. Eusociality in a coral-reef shrimp. Nature 381, 512–514. https://doi.org/10.1038/381512a0 (1996).

    ADS 
    CAS 
    Article 

    Google Scholar 

  • 29.

    Baeza, J. A. & Stotz, W. B. Host-use pattern and host-selection during ontogeny of the commensal crab Allopetrolisthes spinifrons (H. Milne Edwards, 1837) (Decapoda: Anomura: Porcellanidae). J. Nat. Hist. 35, 341–355. https://doi.org/10.1080/002229301300009586 (2001).

    Article 

    Google Scholar 

  • 30.

    Ambrosio, L. J. & Baeza, J. A. Territoriality and conflict avoidance explain asociality (solitariness) of the endosymbiotic pea crab Tunicotheres moseri. PLoS ONE 11, e0148285–e0148285. https://doi.org/10.1371/journal.pone.0148285 (2016).

    CAS 
    Article 
    PubMed 
    PubMed Central 

    Google Scholar 

  • 31.

    Baeza, J. A. & Thiel, M. The mating system of symbiotic crustaceans: A conceptual model based on optimality and ecological constraints. In Evolutionary Ecology of Social and Sexual Systems: Crustaceans as Model Organisms (eds Duffy, J. E. & Thiel, M.) 250–267 (Oxford University Press, 2007).

    Google Scholar 

  • 32.

    Bell, J. L. Distribution and abundance of Dissodactylus mellitae Rathbun (Pinnotheridae) on Mellita quinquiesperforata (Leske)(Echinodermata). J. Exp. Mar. Biol. Ecol. 117, 93–114. https://doi.org/10.1016/0022-0981(88)90220-1 (1988).

    Article 

    Google Scholar 

  • 33.

    Castro, P. Movements between coral colonies in Trapezia ferruginea (Crustacea: Brachyura), an obligate symbiont of scleractinian corals. Mar. Biol. 46, 237–245. https://doi.org/10.1007/BF00390685 (1978).

    Article 

    Google Scholar 

  • 34.

    Baeza, J. A., Simpson, L., Ambrosio, L. J., Guéron, R. & Mora, N. Monogamy in a hyper-symbiotic shrimp. PLoS ONE 11, e0149797. https://doi.org/10.1371/journal.pone.0149797 (2016).

    CAS 
    Article 
    PubMed 
    PubMed Central 

    Google Scholar 

  • 35.

    Diesel, R. Male-female association in the spider crab Inachus phalangium: The influence of female reproductive stage and size. J. Crustac. Biol. 8, 63–69. https://doi.org/10.1163/193724088X00080 (1988).

    Article 

    Google Scholar 

  • 36.

    Wells, H. W. & Wells, M. J. Observations on Pinnaxodes floridensis, a new species of pinnotherid crustacean commensal in holothurians. Bull. Mar. Sci. 11, 267–279 (1961).

    Google Scholar 

  • 37.

    Martin, D. & Britayev, T. A. Symbiotic polychaetes revisited: an update of the known species and relationships (1998–2017). Oceanogr. Mar. Biol. Ann. Rev. 56, 371–448. https://doi.org/10.1201/9780429454455-6 (2018).

    Article 

    Google Scholar 

  • 38.

    Perry, O., Sapir, Y., Perry, G., Ten Hove, H. & Fine, M. Substrate selection of Christmas tree worms (Spirobranchus spp.) in the Gulf of Eilat, Red Sea. J. Mar. Biol. Ass. UK 98, 791–799. https://doi.org/10.1017/S0025315416002022 (2018).

    Article 

    Google Scholar 

  • 39.

    Hunte, W., Colin, B. E. & Marsden, J. R. Habitat selection in the tropical polychaete Spirobranchus giganteus 1 Distribution on corals. Mar. Biol. 104, 87–92 (1990).

    Article 

    Google Scholar 

  • 40.

    Mackie, A. S. Y., Oliver, P. G. & Nygren, A. Antonbruunia sociabilis sp. nov (Annelida: Antonbruunidae) associated with the chemosynthetic deep-sea bivalve Thyasira scotiae Oliver & Drewery, 2014, and a re-examination of the systematic affinities of Antonbruunidae. Zootaxa 3995, 20–36 (2015).

    Article 

    Google Scholar 

  • 41.

    Ruff, R. E. A new species of Bathynoe (Polychaeta: Polynoidae) from the Northeast Pacific Ocean commensal with two species of deep-water asteroids. in: Systematics, Biology and Morphology of World Polychaeta. Proceedings of the Second International Polychaeta Conference. Ophelia Suppl. 5, 219–230 (1991).

  • 42.

    Miura, T. & Ohta, S. Two polychaete species from the deep-sea hydrothermal vent in the Middle Okinawa Trough. Zool. Sci. 8, 383–387 (1991).

    Google Scholar 

  • 43.

    Martin, D., Nygren, A., Hjelmstedt, P., Drake, P. & Gil, J. On the enigmatic symbiotic polychaete “Parasyllideahumesi Pettibone, 1961 (Hesionidae): taxonomy, phylogeny and behaviour. Zool. J. Linn. Soc. 174, 429–446. https://doi.org/10.1111/zoj.12249 (2015).

    Article 

    Google Scholar 

  • 44.

    Chim, C. K., Ong, J. J. L. & Tan, K. S. An association between a hesionid polychaete and temnopleurid echinoids from Singapore. Cah. Biol. Mar. 54, 577–585. https://doi.org/10.21411/CBM.A.ED45E036 (2013).

    Article 

    Google Scholar 

  • 45.

    Goerke, H. Nereis fucata (Polychaeta, Nereidae) als kommensale von Eupagurus bernhardus (Crustacea, Decapoda) Entwicklung einer population und verhalten der art. Veröffentlichungen des Instituts für Meeresforschung in Bremerhaven 13, 79–81 (1971).

    Google Scholar 

  • 46.

    Britayev, T. A., Mekhova, E., Deart, Y. & Martin, D. Do syntopic host species harbour similar symbiotic communities? The case of Chaetopterus spp. (Annelida: Chaetopteridae). PeerJ 5, e2930. https://doi.org/10.7717/peerj.2930 (2017).

    Article 
    PubMed 
    PubMed Central 

    Google Scholar 

  • 47.

    Britayev, T. A., Martin, D., Krylova, E. M., von Cosel, R. & Aksiuk, E. S. Life-history traits of the symbiotic scale-worm Branchipolynoe seepensis and its relationships with host mussels of the genus Bathymodiolus from hydrothermal vents. Mar. Ecol. Evolut. Perspect. 28, 36–48. https://doi.org/10.1111/j.1439-0485.2007.00152.x (2007).

    Article 

    Google Scholar 

  • 48.

    Britayev, T. A. & Zamyshliak, E. A. Association of the commensal scaleworm Gastrolepidia clavigera (Polychaeta: Polynoidae) with holothurians near the coast of South Vietnam. Ophelia 45, 175–190 (1996).

    Article 

    Google Scholar 

  • 49.

    Britayev, T. A. Life cycle of the symbiotic scale-worm Arctonoe vittata (Polychaeta: Polynoidae). In: Systematics, Biology and Morphology of World Polychaeta. Proceedings of the Second International Polychaeta Conference. Ophelia Suppl. 5, 305–312 (1991).

  • 50.

    Devaney, D. M. An ectocommensal polynoid associated with Indo-pacific echinoderms, primarily ophiuroids. Occ. Pap. Bernice P. Bishop Mus. 23, 287–304 (1967).

    Google Scholar 

  • 51.

    Tokaji, H., Nakahara, K. & Goshima, S. Host switching improves survival rate of the symbiotic polychaete Arctonoe vittata. Plank. Bent. Res. 9, 189–196. https://doi.org/10.3800/pbr.9.189 (2014).

    Article 

    Google Scholar 

  • 52.

    Martin, D., Rosell, D. & Uriz, M. J. Harmothoe hyalonemae sp. nov. (Polychaeta, Polynoidae), an exclusive inhabitant of different Atlanto-Mediterranean species of Hyalonema (Porifera, Hexactinellida). Ophelia 35, 169–185 (1992).

    Article 

    Google Scholar 

  • 53.

    Reish, D. J. & Alosi, M. C. Aggressive behavior in the polychaetous annelid family Nereidae. Bull. South. Calif. Acad. Sci. 67, 21–28 (1968).

    Google Scholar 

  • 54.

    Evans, S. M. Behavior in polychaetes. Q. Rev. Biol. 46, 379–405 (1971).

    Article 

    Google Scholar 

  • 55.

    Scaps, P. Intraspecific agonistic behaviour in the polychaete Perinereis cultrifera (Grübe). Vie et Milieu 45, 123–128 (1995).

    Google Scholar 

  • 56.

    Johnson, H. P. A preliminary account of the marine annelids of the Pacific coast, with descriptions of new species. Proc. Calif. Acad. Sci. 1, 153–199 (1897).

    Google Scholar 

  • 57.

    Miers, E. J. Report on the Brachyura collected by HMS Challenger during the years 1873–1876. in: Report on the scientific results of the Voyage of HMS Challenger during the years 1873–76 under the command of Captain George S. Nares, R. N., F.R.S. and the late Captain Frank Tourle Thompson, R. N. Zoology 17, 1–363, pls. 361–329 (1886).

  • 58.

    Latreille, P. A. Trapezie. in Entomologie, ou histoire naturelle des crustaces, des arachnides et des insectes, Vol. 10 695–696 (Encyclopedie Methodique, Histoire Naturelle, 1828).

  • 59.

    Petersen, M. E. & Britayev, T. A. A new genus and species of polynoid scaleworm commensal with Chaetopterus appendiculatus Grube from the Banda Sea (Annelida: Polychaeta), with a review of commensals of Chaetopteridae. Bull. Mar. Sci. 60, 261–276 (1997).

    Google Scholar 

  • 60.

    Grube, A. E. Descriptiones Annulatorum novorum mare Ceylonicum habitantium ab honoratissimo Holdsworth collectorum. Proc. Zool. Soc. Lond. 41, 325–329. https://doi.org/10.1111/j.1096-3642.1874.tb02492.x (1874).

    Article 

    Google Scholar 

  • 61.

    Britayev, T. A. & Martin, D. Scale-worms (Polychaeta, Polynoidae) associated with chaetopterid worms (Polychaeta, Chaetopteridae), with description of a new genus and species. J. Nat. Hist. 39, 4081–4099. https://doi.org/10.1080/00222930600556229 (2005).

    Article 

    Google Scholar 

  • 62.

    Grant, J. W. A., Gaboury, C. L. & Levitt, H. L. Competitor-to-resource ratio, a general formulation of operational sex ratio, as a predictor of competitive aggression in Japanese medaka (Pisces: Oryziidae). Behav. Ecol. 11, 670–675. https://doi.org/10.1093/beheco/11.6.670 (2000).

    Article 

    Google Scholar 

  • 63.

    Britayev, T. A. & Smurov, A. V. Distribution and relocation of commensal crabs Pinnixa rathbhuni (Pinnotheridae) on their hosts. Dokl. Akad. Nauk SSSR 300, 1506–1509 (1988).

    Google Scholar 

  • 64.

    Walker, A. O. Notes on a collection of Crustacea from Singapore. J. Linn. Soc. Lond. Zool. 20, 107–117. https://doi.org/10.1111/j.1096-3642.1887.tb01440.x (1887).

    Article 

    Google Scholar 

  • 65.

    Kemp, D. J. Habitat selection and territoriality. In Insect behavior: from mechanisms to ecological and evolutionary consequences (eds Córdoba-Aguilar, A. et al.) 80–97 (Oxford University Press, 2018).

    Google Scholar 

  • 66.

    Jumars, P. A., Dorgan, K. M. & Lindsay, S. M. Diet of worms emended: An update of polychaete feeding guilds. Ann. Rev. Mar. Sci. 7, 497–520. https://doi.org/10.1146/annurev-marine-010814-020007 (2015).

    Article 
    PubMed 

    Google Scholar 

  • 67.

    Cotter, E., O’Riordan, R. M. & Myers, A. A. A histological study of reproduction in the serpulids Pomatoceros triqueter and Pomatoceros lamarckii (Annelida: Polychaeta). Mar. Biol. 142, 905–914 (2003).

    Article 

    Google Scholar 

  • 68.

    Prevedelli, D., Massamba N’Siala, G., Ansaloni, I. & Simonini, R. Life cycle of Marphysa sanguinea (Polychaeta: Eunicidae) in the Venice Lagoon (Italy). Mar. Ecol. 28, 384–393. https://doi.org/10.1111/j.1439-0485.2007.00160.x (2007).

    ADS 
    Article 

    Google Scholar 

  • 69.

    Bergman, D. A. & Moore, P. A. Prolonged exposure to social odours alters subsequent social interactions in crayfish (Orconectes rusticus). Anim. Behav. 70, 311–318. https://doi.org/10.1016/j.anbehav.2004.10.026 (2005).

    Article 

    Google Scholar 

  • 70.

    Arakaki, J. Y. et al. Battle of the borders: Is a range-extending fiddler crab affecting the spatial niche of a congener species?. J. Exp. Mar. Biol. Ecol. 532, 151445. https://doi.org/10.1016/j.jembe.2020.151445 (2020).

    Article 

    Google Scholar 

  • 71.

    Britayev, T. A. & Mekhova, E. S. Do symbiotic polychaetes migrate from host to host?. Mem. Mus. Victoria 71, 21–25 (2014).

    Article 

    Google Scholar 

  • 72.

    Livermore, J., Perreault, T. & Rivers, T. Luminescent defensive behaviors of polynoid polychaete worms to natural predators. Mar. Biol. 165, 149. https://doi.org/10.1007/s00227-018-3403-2 (2018).

    Article 

    Google Scholar 

  • 73.

    Daly, J. M. Segmentation, autotomy and regeneration of lost posterior segments in Harmothoe imbricata (L) (Polychaeta: Polynoidae). QH1.M454 1, 17–28 (1973).

    Google Scholar 

  • 74.

    Schiaparelli, S., Alvaro, M. C. & Barnich, R. Polynoid polychaetes living in the gut of irregular sea urchins: A first case of inquilinism in the Southern Ocean. Antarct. Sci. 23, 144–151. https://doi.org/10.1017/S0954102011000083 (2011).

    ADS 
    Article 

    Google Scholar 

  • 75.

    Sokal, R. R. & Rohlf, F. J. Biometry. The Principles and Practice of Statistics in Biological Research 3rd edn. (W.H. Freeman and Company, 1995).

    MATH 

    Google Scholar 

  • 76.

    Everitt, B. The Analysis of Contingency Tables 2nd edn. (Chapman & Hall, 1992).

    Book 

    Google Scholar 


  • Source: Ecology - nature.com

    Southward decrease in the protection of persistent giant kelp forests in the northeast Pacific

    Integrating spatial analysis and questionnaire survey to better understand human-onager conflict in Southern Iran