Oecologia

, Volume 149, Issue 1, pp 174–184 | Cite as

Dispersal strategies in sponge larvae: integrating the life history of larvae and the hydrologic component

  • Simone Mariani
  • María-J. Uriz
  • Xavier Turon
  • Teresa Alcoverro
Behavioural Ecology

Abstract

While known to be uniformly non-feeding, short-lived, and potentially short dispersing, sponge larvae display different behaviours (swimming ability and taxis). Our aim was to show whether sponge larvae with different behaviours exhibit different dispersal strategies under variable intensity of water movements. We first assessed the distribution of larvae of six taxa: Dictyoceratida spp., Dysidea avara, Crambe crambe, Phorbas tenacior, Scopalina lophyropoda, and Cliona viridis, collected through plankton sampling, and the abundance of the corresponding adult sponges across three hard bottom communities and a sandy bottom from a north-west Mediterranean rocky shore. We then tested adult–larvae couplings (abundance of larvae vs abundance of adults) under increasing levels of water movements (surge) to assess the importance of this environmental factor in driving differences in dispersal strategies. Adults of Dictyoceratida spp., D. avara, and P. tenacior were most abundant in semi-dark caves (SDC), C. crambe and C. viridis in communities of sciaphilic algae (SA), whereas the distribution of S. lophyropoda was extremely patchy, being present almost only in the SA community of one of the five stations studied. Larvae of Dictyoceratida spp. and P. tenacior were more abundant in the SDC, whereas D. avara and C. crambe were homogeneously distributed across the communities. The larvae of C. viridis were more abundant in the SA communities and the S. lophyropoda larvae were mostly present in one station and one community (SA). Increased water movement did not modify the adult–larvae coupling for Dictyoceratida spp., D. avara, and C. crambe, whereas it broke up the positive association for P. tenacior and to some extent S. lophyropoda. For C. viridis, possible variability in adult–larvae coupling was not tested because the larvae were collected on only one day under calm sea conditions. We confirm that efficient-swimming larvae with some cue response can actively counteract hydrodynamic forces and highlight the importance of both larval behaviour and environmental conditions in determining small-scale patterns of dispersal.

Keywords

Behaviour Marine invertebrates Mediterranean Sea Plankton Water movement 

References

  1. Abelson A, Denny M (1997) Settlement of marine organisms in flow. Annu Rev Ecol Syst 28:317–339CrossRefGoogle Scholar
  2. Amano S (1986) Larval release in response to a light signal by the intertidal sponge Halichondria panicea. Biol Bull 171:371–378CrossRefGoogle Scholar
  3. Amano S (1988) Morning release of larvae controlled by the light in an intertidal sponge, Callyspongia ramosa. Biol Bull 175:181–184CrossRefGoogle Scholar
  4. Becerro MA, Uriz MJ, Turon X (1994) Trends in space occupation by the encrusting sponge Crambe crambe: variation in shape as a function of size and environment. Mar Biol 121:301–307CrossRefGoogle Scholar
  5. Bergquist PR, Sinclair ME (1968) The morphology and behaviour of larvae of some intertidal sponges. NZ J Mar Freshw Res 2:426–437CrossRefGoogle Scholar
  6. Bergquist PR, Sinclair ME, Hogg JJ (1970) Adaptation to intertidal existence: reproductive cycles and larval behaviour in Demospongiae. Symp Zool Soc Lond 25:247–271Google Scholar
  7. Boury-Esnault N, Rützler K (1997) Thesaurus of sponge morphology. Smith Contr Zool 596:1–55Google Scholar
  8. Burdett-Coutts V, Metaxas A (2004) The effect of the quality of food patches on vertical distribution of the sea urchins Lytechinus variegatus (Lamark) and Strongylocentrotus droebachensis (Mueller). J Exp Mar Biol Ecol 308:221–236CrossRefGoogle Scholar
  9. Fisher R (2005) Swimming speeds of larval coral reef fishes: impacts of self-recruitment and dispersal. Mar Ecol Prog Ser 285:223–232CrossRefGoogle Scholar
  10. Gilg MR, Hilbish TJ (2003) The geography of marine larval dispersal: coupling genetics with fine-scale physical oceanography. Ecology 84:2989–2998CrossRefGoogle Scholar
  11. Graham KR, Sebens KP (1996) The distribution of marine invertebrate larvae near vertical surfaces in the rocky subtidal zone. Ecology 77:933–949CrossRefGoogle Scholar
  12. Grosberg RK (1987) Limited dispersal and proximity-dependent mating success in the colonial ascidian Botryllus shlosseri. Evolution 41:372–384CrossRefGoogle Scholar
  13. Jackson JBC (1985) Distribution and ecology of clonal and aclonal benthic invertebrates. In: Jackson JBC, Buss LW, Cook E (eds) Population biology and evolution of clonal organisms. Yale University, New Haven, pp 297–356Google Scholar
  14. Keough MJ (1986) The distribution of a bryozoan on seagrass blades: settlement, growth, and mortality. Ecology 67:846–857CrossRefGoogle Scholar
  15. Keough MJ, Black KP (1996) Predicting the scale of marine impacts: Understanding planktonic links between population. In: Schmitt RJ, Osenberg CW (eds) The design of ecological impact studies: conceptual issues and application in coastal marine habitats. Academic, Orlando, pp 199–234Google Scholar
  16. Leis JM, Sweatman HPA, Reader SE (1996) What pelagic stages of coral reef fishes are doing in the blue water: daytime field observations of larval behavioural capabilities. Mar Freshw Res 47:401–411CrossRefGoogle Scholar
  17. Levin LA, Huggett D, Myers P, Bridges T, Weaver J (1993) Rare-earth tagging methods for the study of larval dispersal by marine invertebrates. Limnol Oceanogr 38:346-360CrossRefGoogle Scholar
  18. Leys SP, Degnan BM (2001) Cytological basis of photoresponsive behavior in a sponge larva. Biol Bull 201:323–338PubMedCrossRefGoogle Scholar
  19. Lindquist N, Hay ME (1996) Palatability and chemical defence of marine invertebrate larvae. Ecol Monogr 62:547–568CrossRefGoogle Scholar
  20. Linquist N, Bolser RC, Laing K (1997) Timing of larval release by two Caribbean demosponges. Mar Ecol Prog Ser 155:309–316CrossRefGoogle Scholar
  21. Maldonado M, Bergquist PR (2002) Phylum porifera. In: Young CM (ed) Atlas of marine invertebrate larvae. Academic, London, pp 21–50Google Scholar
  22. Maldonado M, Uriz MJ (1998) Microrefuge explotation by subtidal encrusting sponges: patterns of settlement and post-settlement survival. Mar Ecol Prog Ser 174:141–150CrossRefGoogle Scholar
  23. Maldonado M, Young CM (1996) Effects of physical factors on larval behavior, settlement and recruitment of four tropical demosponges. Mar Ecol Prog Ser 138:169–180CrossRefGoogle Scholar
  24. Maldonado M, Durfort M, McCarty DA, Young CM (2003) The cellular basis of photobehavior in the tufted parenchymella larva of demosponges. Mar Biol 143:427–441CrossRefGoogle Scholar
  25. Mariani S (2002) Larval supply and recruitment of invertebrates in the western Mediterranean: patterns in contrasting benthic communities. PhD thesis, University of BarcelonaGoogle Scholar
  26. Mariani S (2003) Recruitment in invertebrates with short-lived larvae: the case of the bryozoan Disporella hispida (Fleming). Helgol Mar Res 57:47–53Google Scholar
  27. Mariani S, Uriz MJ, Turon X (2000) Larval bloom of the oviparous sponge Cliona viridis: coupling of larval abundance and adult distribution. Mar Biol 137:783–790CrossRefGoogle Scholar
  28. Mariani S, Piscitelli M, Uriz MJ (2001) Temporal and spatial co-occurrence in spawning and larval release of Cliona viridis (Porifera: Hadromerida). J Mar Biolog Assoc UK 81:365–367Google Scholar
  29. Mariani S, Uriz MJ, Turon X (2003) Methodological bias in the estimations of important meroplanktonic components from near-shore bottoms. Mar Ecol Prog Ser 253:67–75CrossRefGoogle Scholar
  30. Mariani S, Uriz MJ, Turon X (2005a) The dynamics of sponge larvae assemblages from northwestern Mediterranean nearshore bottms. J Plankt Res 27:249–262CrossRefGoogle Scholar
  31. Mariani S, Alcoverro T, Uriz M-J, Turon X (2005b) Early life histories in the bryozoan Scizobrachiella sanguinea: a case study. Mar Biol 147:735–745CrossRefGoogle Scholar
  32. Metaxas A (2001) Behaviour in flow: perspectives on the distribution and dispersion of meroplanktonic larvae in the water column. Can J Fish Aquat Sci 58:86–98CrossRefGoogle Scholar
  33. Olson RR (1985) The consequences of short-distance larval dispersal in a sessile marine invertebrate. Ecology 66:30–39CrossRefGoogle Scholar
  34. Olson RR, McPherson R (1987) Potential vs. realized larval dispersal: fish predation on larvae of the ascidian Lissoclinum patella (Gottshaldt). J Exp Mar Biol Ecol 110:245–256CrossRefGoogle Scholar
  35. Paris CB, Cowen RK (2004) Direct evidence of a biophysical retention mechanism for coral reef fish larvae. Limnol Oceanogr 49:1964–1979CrossRefGoogle Scholar
  36. Raimondi PT (1991) Settlement behavior of Chtamalus anisopoma larvae largely determines the adult distribution. Oecologia 85:349–360CrossRefGoogle Scholar
  37. Stoner DS (1990) Recruitment of a tropical colonial ascidian: relative importance of pre-settlement vs. post settlement processes. Ecology 71:1682–1690CrossRefGoogle Scholar
  38. Stoner DS (1992) Vertical distribution of a colonial ascidian on a coral reef: the roles of larval dispersal and life-history variation. Am Nat 139:802–824CrossRefGoogle Scholar
  39. Svane I, Young CM (1989) The ecology and behaviour of ascidian larvae. Ocean Mar Biol Annu Rev 27:45–90Google Scholar
  40. Underwood AJ, Keough (2002) Supply-side ecology. The nature and consequences of variations in recruitment of intertidal organisms. In: Bertness MD, Gaines SD, Hay ME (eds) Marine community ecology. Sinauer, Sunderland, pp 183–200Google Scholar
  41. Uriz MJ, Rosell D, Martin D (1992) The sponge population of the Cabrera archipelago (Balearic Islands): characteristics, distribution, and abundance of the most representative species. PSZNI Mar Ecol 13:101–117CrossRefGoogle Scholar
  42. Uriz MJ, Turon X, Becerro MA, Galera J, Lozano J (1996) Feeding deterrence in sponges. The role of toxicity, physical defences, energetic contents, and life-history stage. J Exp Mar Biol Ecol 205:187–204CrossRefGoogle Scholar
  43. Uriz MJ, Maldonado M, Turon X, Martí R (1998) How do reproductive output, larval behaviour, and recruitment contribute to adult spatial patterns in Mediterranean encrusting sponges? Mar Ecol Prog Ser 167:137–148CrossRefGoogle Scholar
  44. Uriz MJ, Turon X, Becerrro MA (2001) Morphology and ultrastructure of the swimming larvae of Crambe crambe (Demospongiae, Poecillosclerida). Invertebr Biol 120:295–307CrossRefGoogle Scholar
  45. Young CM, Chia FS (1987) Abundance and distribution of pelagic larvae as influenced by predation, behavior, and hydrogeographic factors. In: Giese AC (ed) Reproduction of marine invertebrates, vol 9. Blackwell, Palo Alto, pp 385–464Google Scholar
  46. Zea S (1993) Recruitment of Demosponges (Porifera, Demospongiae) in rocky and coral reef habitats of Santa Marta, Colombian Carribean. PSZNI Mar Ecol 14:1–21CrossRefGoogle Scholar

Copyright information

© Springer-Verlag 2006

Authors and Affiliations

  • Simone Mariani
    • 1
  • María-J. Uriz
    • 1
  • Xavier Turon
    • 2
  • Teresa Alcoverro
    • 1
  1. 1.Centre d’Estudis Avançats de Blanes (CSIC)BlanesSpain
  2. 2.Departament de Biologia Animal (Invertebrats), Facultat de BiologiaUniversitat de BarcelonaBarcelonaSpain

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