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Recolonization of the Himerometra robustipinna (Himerometridae, Crinoidea) by macrosymbionts: an in situ experiment

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Abstract

It is generally considered that symbiotic organisms colonize their hosts during their early stages of development. The main goals of the present study were to assess whether post-settled (juvenile and adult) symbionts were able to colonize comatulid crinoids, and whether a hosts’ spatial distribution may influence the colonization pattern through a series of field recolonization experiments. Three series of experiments on recolonization of the comatulid crinoid Himerometra robustipinna were conducted in the Nhatrang Bay, South-China Sea, Vietnam. Ten species of macrosymbiont, 1 polychaetes, 1 gastropods, 1galatheids, 1 ophiurids, and 6 shrimps were found to be associated with H. robustipinna host in the controls and in the 3 experimental series. We found that symbionts rapidly colonized depopulated crinoids in all the experimental series. The prevalence was lower in the experimental series than in the controls butthe abundance, species richness were not significantly different. The presence of post-settled juveniles and adults in experimental series indicated migration from neighboring hosts. Dispersal strategies of symbionts varied: some of them such as the polychaete Paradyte crinoidicola, the gastropod Annulobalcis vinarius, and the galatheid Allogalathea elegans were rapid colonizers. The shrimps Periclimenes commensalis, Pontoniopsis comanthi, and ophiuroid Gymnolophus obscura demonstrated low colonization rate. The 1 and 2 experimental series showed that there was movement of symbionts in dense hosts’ aggregations or over short distances. Unexpectedly, the infestation characteristics of crinoids in the spatially isolated site (series 3) didn’t differ from that of crinoids from aggregations (series 1 and 2), which indicates that long distance (tens meters) migrations of crinoid symbionts also occurs.

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References

  • Britayev TA (1991) Life cycle of the symbiotic scaleworm Arctonoe vittata (Polychaeta: Polynoidae). Ophelia 5:305–312

    Google Scholar 

  • Britayev TA, Mekhova ES (2011) Assessment of hidden diversity of crinoids and their symbionts in the Bay of Nhatrang, Vietnam. Org Divers Evol 11:275–285

    Article  Google Scholar 

  • Britayev TA, Mikheev VN (2013) Clumped spatial distribution of scleractinian corals influences structure of their symbiotic associations. Dokl Biol Sci 448 (in print)

  • Castro P (1978) Movements between corals colonies in Trapezia ferruginia (Crustacea: Brachyura), an obligate symbiont of scleractinian corals. Mar Biol 46:237–245

    Article  Google Scholar 

  • Coles SL (1980) Species diversity of Decapods associated with living and dead reef coral Pocillopora meandrina. Mar Ecol Prog Ser 2:281–291

    Article  Google Scholar 

  • Davenport D (1950) Studies in the physiology of commensalism. I. The polynoid genus Arctonoë. Biol Bull Mar Biol Lab Woods Hole 98:81–93

    Article  CAS  Google Scholar 

  • De Bruyn C, Rigaud T, David B, De Ridder C (2009) Symbiosis between the pea crab Dissodactylus primitivus and its echinoid host Meoma ventricosa: potential consequences for the crab mating system. Mar Ecol Prog Ser 375:173–183

    Article  Google Scholar 

  • De Bruyn C, De Ridder C, Rigaud T, David B (2011) Chemical host detection and differential attraction in a parasitic pea crab infecting two echinoids. J Exp Mar Biol Ecol 397:173–178

    Article  Google Scholar 

  • Deheyn D, Lyskin SA, Eeckhaut I (2006) Assemblages of symbionts in tropical shallow-water crinoids and assessment of symbionts’ host specificity. Symbiosis 42:161–168

    Google Scholar 

  • Dimock RV Jr, Davenport D (1971) Behavioral specificity and the induction of host recognition in a symbiotic polychaete. Biol Bull Mar Biol Laboratory Woods Hole 141:472–484

    Article  Google Scholar 

  • Edgar GJ (1992) Patterns of colonization of mobile epifauna in a Western Australian seagrass bed. J Exp Mar Biol Ecol 157:225–246

    Article  Google Scholar 

  • Eggleston DB, Elis WE, Etherington LL, Dahlgren CP, Posey MH (1999) Organism responses to habitat fragmentation and diversity: habitat colonization by estuarine macrofauna. J Exp Mar Biol Ecol 236:107–132

    Article  Google Scholar 

  • Fabricius KE, Dale MB (1993) Multispecies associations of symbionts on shallow water crinoids of the central Great Barrier Reef. Cenoses 8(1):41–52

    Google Scholar 

  • Fishelson L (1985) Ecology of Red Sea crinoids and their epi- and endozoic fauna. Mar Biol 28(2):183–192

    Google Scholar 

  • Glynn PW, Stewart RH, McCosker JE (1972) Pacific coral reefs of Panama: structure, distribution, and predators. Geol Rundsch 61: 483–519

    Google Scholar 

  • Gustafsson C, Salo T (2012) A latitudinal comparison on the effect of distance on faunal colonization in seagrass ecosystems. Mar Biol 159:1497–1507

    Article  Google Scholar 

  • Hoeksema BW, van der Land J, van der Meij SET, Ofwegen LP, Reijnen BT, van Soest RWM, de Voogd NJ (2011) Unforeseen importance of historical collections as baselines to determine biotic change of coral reefs: the Saba Bank case. Mar Ecol 32:135–141

    Article  Google Scholar 

  • Huang HD, Rittschof D, Jeng MS (2005) Multispecies associations of macrosymbionts on the comatulid crinoids Comanthina schlegeli (Carpenter) in Southern Taiwan. Symbiosis 39:47–51

    Google Scholar 

  • Jangoux M (1990) Diseases of Echinodermata. In: Kinne O (ed) Diseases of Echinodermata, vol 3. Biologische Anstalt Helgoland, Hamburg, pp 439–567

    Google Scholar 

  • MacDonald KS, Rios R, Duffy JE (2006) Biodiversity, host specificity, and dominance by eusocial species among sponge-dwelling alpheid shrimp on the Belize Barrier Reef. Divers Distrib 12:165–178

    Article  Google Scholar 

  • Mekhova ES, Britayev TA (2012) Feather stars (Crinoidea, Comatulida) of Nhatrang Bay, Vietnam; fauna, habitat and symbionts. In: Britayev TA, Pavlov DS (eds) Benthic fauna of the Bay of Nhatrang, Southern Vietnam, vol 2. KMK Scientific Press, Moscow, p 447–478

  • Messing CG (1994) Comatulid crinoids (Echinodermata) of Madang, Papua New Guinea, and environs: diversity and ecology. In: David B, Guille A, Feral J-P, Roux M (eds) Echinoderms through time. Balkema, Rotterdam, pp 237–243

    Google Scholar 

  • Messing CG, Meyer DL, Siebeck UE, Jermiin LS, Vaney DI, Rouse GW (2006) A modern soft-bottom, shallow-water crinoid fauna (Echinodermata) from the Great Barrier Reef, Australia. Coral Reefs 25:164–168

    Article  Google Scholar 

  • Patton WK (1994) Distribution and ecology of animals associatedwith branching corals (Acropora spp.) from the Great BarrierReef, Australia. Bull Mar Sci 55:193–211

    Google Scholar 

  • Rasmussen E (1973) Systematics and ecology of the Isefjord marine fauna (Denmark). Ophelia 11:495p

    Article  Google Scholar 

  • Russell BD, Gillanders BM, Connell SD (2005) Proximity and size of neighbouring habitat affects invertebrate diversity. Mar Ecol Prog Ser 296:31–38

    Article  Google Scholar 

  • Sorokin IY (1990) Aspects of trophic relations, productivity and energy balance in coral-reef ecosystems. In: Dubinski Z (ed) Ecosystems of the world: coral reefs, vol 25. Elsevier, Amsterdam, pp 401–409

    Google Scholar 

  • Stella JS, Jones GP, Pratchett MS (2010) Variation in the structure of epifaunal invertebrate assemblages among coral hosts. Coral Reefs 29:957–973

    Article  Google Scholar 

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

    Google Scholar 

  • Thorson G (1946) Reproduction and larval development of Danish marine bottom invertebrates with special reference to the planktonic larvae in the Sound (Oresund). Medd Dan Fisk-Havunder. Ser Placton 4:1–523

    Google Scholar 

  • Trzcinski MK, Fahrig L, Merriam G (1999) Independent effects of forest cover and fragmentation on the distribution of forest breeding birds. Ecol Appl 9:586–593

    Article  Google Scholar 

  • VandenSpiegel D, Eeckhaut I, Jangoux M (1998) Host selection by Synalpheus stimpsoni (De Man), an ectosymbiotic shrimp of comatulid crinoids, inferred by a field survey and laboratory experiments. J Exp Mar Biol Ecol 225:185–196

    Article  Google Scholar 

  • Virnstein RW, Curran MC (1986) Colonization of artificial seagrass versus time and distance from source. Mar Ecol Prog Ser 29:279–288

    Article  Google Scholar 

  • Warén A (1983) A generic revision of the family Eulimidae (Gastropoda, Prosobranchia). J Mollus Stud 49(Suppl. 13):1–96

    Google Scholar 

  • Yanagisawa Y, Hamaishi A (1986) Mate acquisition by a solitary crab Zebrida adamsii, a symbiont of the sea urchin. J Ethol 4:153–162

    Article  Google Scholar 

Download references

Acknowledgments

We would like to thank the Russian-Vietnam Tropical Center of A.N. Severtsov Institute of Ecology and Evolution of Russian Academy of Sciences (SIEE) for the opportunity to make this investigation, O.V. Savinkin (SIEE) and our colleagues from the Laboratory of Morphology and Ecology of Marine Invertebrates of SIEE for technical and field assistance, Yu.V. Deart for help with statistical analysis, Dr. V.N. Mikheev and two anonymous reviewers for valuable editorial advices and improvement of the manuscript,. The study was supported by the Russian Foundation for Basic Research, under grants 12-05-00239, 12-04-31017 and by the Ministry of Education and Science of Russian Federation (contract No 16.512.11.2133).

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Correspondence to P. Yu. Dgebuadze.

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Dgebuadze, P.Y., Mehova, E.S. & Britayev, T.A. Recolonization of the Himerometra robustipinna (Himerometridae, Crinoidea) by macrosymbionts: an in situ experiment. Symbiosis 58, 253–258 (2012). https://doi.org/10.1007/s13199-013-0227-1

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