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Fish predation on sea urchins on the Great Barrier Reef

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Abstract

Predators are important for regulating adult sea urchin densities. Here, we employ remote underwater video cameras to record diurnal predation on tethered sea urchins at Lizard Island on the Great Barrier Reef (GBR). We identified four fish predators of adult sea urchins (Balistoides viridescens, Balistapus undulatus, Lethrinus atkinsoni and Choerodon schoenleinii). Predator activity appeared to be site-specific. Balistoides viridescens and B. undulatus (f: Balistidae) were the two most important predators of Echinometra mathaei with the former handling E. mathaei significantly faster (mean 0.7 min) than B. undulatus (5.2 min). Balistoides viridescens also successfully preyed on 70 % of detections, while C. schoenleinii, B. undulatus and L. atkinsoni preyed on just 33, 17 and <1 %, respectively. Additionally, B. viridescens were behaviourally dominant among predator species and were observed as aggressors in 30 encounters with B. undulatus and 8 encounters with L. atkinsoni. In only one encounter was B. viridescens the recipient of any aggression (from B. undulatus). In terms of relative vulnerability, of the three sea urchin species examined, E. mathaei were more vulnerable to predation than Diadema setosum or Echinothrix calamaris, with mean handling times of 1.2, 4.8 and 10.3 min, respectively. Balistoides viridescens and B. undulatus both appear to be able to play an important role as predators of sea urchins on the relatively intact coral reefs of Lizard Island. However, B. viridescens emerge as the most efficient predator in terms of handling speed and the proportion of detections preyed upon. They were also the behaviourally dominant predator. This preliminary study of the predators of sea urchins on the GBR highlights the potential significance of relatively scarce but functionally important species.

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References

  • Aronson RB, Heck KL (1995) Tethering experiments and hypothesis testing in ecology. Mar Ecol Prog Ser 121:307–309

    Article  Google Scholar 

  • Bak RPM (1994) Sea urchin bioerosion on coral reefs: place in the carbonate budget and relevant variables. Coral Reefs 13:99–103

    Article  Google Scholar 

  • Bellwood DR, Hughes TP, Folke C, Nystrom M (2004) Confronting the coral reef crisis. Nature 429:827–833

    Article  PubMed  CAS  Google Scholar 

  • Bonaviri C, Fernández TV, Badalamenti F, Gianguzza P, Di Lorenzo M, Riggio S (2009) Fish versus starfish predation in controlling sea urchin populations in Mediterranean rocky shores. Mar Ecol Prog Ser 382:129–138

    Article  Google Scholar 

  • Brodie ED, Formanowicz DR, Brodie ED (1991) Predator avoidance and antipredator mechanisms: distinct pathways to survival. Ethol Ecol Evol 3:73–77

    Article  Google Scholar 

  • Carreiro-Silva M, McClanahan TR (2001) Echinoid bioerosion and herbivory on Kenyan coral reefs: the role of protection from fishing. J Exp Mar Biol Ecol 262:133–153

    Article  PubMed  Google Scholar 

  • Clemente S, Hernández JC, Toledo K, Brito A (2007) Predation upon Diadema aff. antillarum in barren grounds in the Canary Islands. Sci Mar 71:745–754

    Google Scholar 

  • Clemente S, Hernández JC, Rodriguez A, Brito A (2010) Identifying keystone predators and the importance of preserving functional diversity in sublittoral rocky-bottom areas. Mar Ecol Prog Ser 413:55–67

    Article  Google Scholar 

  • Clemente S, Hernández JC, Brito A (2011) Context-dependent effects of marine protected areas on predatory interactions. Mar Ecol Prog Ser 437:119–133

    Article  Google Scholar 

  • Coppard SE, Campbell AC (2005) Distribution and abundance of regular sea urchins on two coral reefs in Fiji. Micronesica 37:249–269

    Google Scholar 

  • Downing N, El-Zahr CR (1987) Gut evacuation and filling rates in the rock-boring sea urchin, Echinometra mathaei. Bull Mar Sci 41:579–584

    Google Scholar 

  • Eakin CM (1996) Where have all the carbonates gone? A model comparison of calcium carbonate budgets before and after the 1982–1983 El Nino at Uva Island in the eastern Pacific. Coral Reefs 15:109–119

    Google Scholar 

  • Fairweather PG, Underwood AJ (1983) The apparent diet of predators and biases due to different handling times of their prey. Oecologia 56:169–179

    Article  Google Scholar 

  • Fricke HW (1971) Fische als feinde tropischer seeigel. Mar Biol 9:328–338

    Article  Google Scholar 

  • Guidetti P (2004) Consumers of sea urchins, Paracentrotus lividus and Arbacia lixula, in shallow Mediterranean rocky reefs. Helgol Mar Res 58:110–116

    Article  Google Scholar 

  • Guidetti P (2007) Predator diversity and density affect levels of predation upon strongly interactive species in temperate rocky reefs. Oecologia 154:513–520

    Article  PubMed  Google Scholar 

  • Hiatt RW, Strasburg DW (1960) Ecological relationships of the fish fauna on coral reefs of the Marshall Islands. Ecol Monogr 30:65–127

    Article  Google Scholar 

  • Hobson ES (1975) Feeding patterns among tropical reef fishes: understanding the way fishes respond to changing conditions during the day-night cycle provides insight into their feeding activities. Am Sci 63:382–392

    Google Scholar 

  • Hoyle JA, Keast A (1987) The effect of prey morphology and size on handling time in a piscivore, the largemouth bass (Micropterus salmoides). Can J Zool 65:1972–1977

    Article  Google Scholar 

  • Hughes TP (1994) Catastrophes, phase shifts, and large-scale degradation of a Caribbean coral reef. Science 265:1547–1551

    Article  PubMed  CAS  Google Scholar 

  • Hughes RN (1997) Diet selection. In: Godin JGJ (ed) Behavioural ecology of teleost fishes. Oxford University Press, New York, pp 134–162

    Google Scholar 

  • Matsuura K (2001) Balistidae: triggerfishes. In: Carpenter K, Niem V (eds) FAO species identification guide for fishery purposes: the living marine resources of the Western Central Pacific, Vol 6. FAO, Rome

    Google Scholar 

  • McClanahan TR (1988) Coexistence in a sea urchin guild and its implications to coral reef diversity and degradation. Oecologia 77:210–218

    Article  Google Scholar 

  • McClanahan TR (1995) Fish predators and scavengers of the sea urchin Echinometra mathaei in Kenyan coral-reef marine parks. Environ Biol Fishes 43:187–193

    Article  Google Scholar 

  • McClanahan TR (1999) Predation and the control of the sea urchin Echinometra viridis and fleshy algae in the patch reefs of Glovers Reef, Belize. Ecosystems 2:511–523

    Article  Google Scholar 

  • McClanahan TR (2000) Recovery of a coral reef keystone predator, Balistapus undulatus, in East African marine parks. Biol Conserv 94:191–198

    Article  Google Scholar 

  • McClanahan TR, Muthiga NA (1989) Patterns of predation on a sea urchin, Echinometra mathaei (de Blainville), on Kenyan coral reefs. J Exp Mar Biol Ecol 126:77–94

    Article  Google Scholar 

  • McClanahan TR, Muthiga NA (2001) The ecology of Echinometra. In: Lawrence JM (ed) Edible sea urchins: biology and ecology. Elsevier Science, Amsterdam, pp 225–243

    Chapter  Google Scholar 

  • McClanahan TR, Shafir SH (1990) Causes and consequences of sea urchin abundance and diversity in Kenyan coral reef lagoons. Oecologia 83:362–370

    Google Scholar 

  • McClanahan TR, Nugues M, Mwachireya S (1994) Fish and sea urchin herbivory and competition in Kenyan coral reef lagoons: the role of reef management. J Exp Mar Biol Ecol 184:237–254

    Article  Google Scholar 

  • Parker D, Shulman M (1986) Avoiding predation: alarm responses of Caribbean sea urchins to simulated predation on conspecific and heterospecific sea urchins. Mar Biol 93:201–208

    Article  Google Scholar 

  • Pederson HG, Johnson CR (2006) Predation of the sea urchin Heliocidaris erythrogramma by rock lobsters (Jasus edwardsii) in no-take marine reserves. J Exp Mar Biol Ecol 336:120–134

    Article  Google Scholar 

  • Randall JE (1967) Food habits of reef fishes of the West Indies. In: Bayer FM, Idyll CP, Jones JI, Koczy FF, Myrberg AA, Richard Robins C, Walton Smith FG, Voss GL, Ferguson Wood EJ, Jenses AC (eds) Proceedings of the International Conference on Tropical Oceanography: Studies In Tropical Oceanography, Miami, pp 665–847

  • Randall JE, Head SM, Sanders APL (1978) Food habits of the giant humphead wrasse. Environ Biol Fishes 3:235–238

    Article  Google Scholar 

  • Randall JE, Allen GR, Steene RC (1990) Fishes of the Great Barrier Reef and Coral Sea. University of Hawaii Press, Honolulu

    Google Scholar 

  • Sala E (1997) Fish predators and scavengers of the sea urchin Paracentrotus lividus in protected areas of the north-west Mediterranean Sea. Mar Biol 129:531–539

    Article  Google Scholar 

  • Sala E, Zabala M (1996) Fish predation and the structure of sea urchin Paracentrotus lividus populations in the NW Mediterranean. Mar Ecol Prog Ser 140:71–81

    Article  Google Scholar 

  • Sih A (1987) Predators and prey lifestyles: an evolutionary and ecological overview. In: Kerfoot WC, Sih A (eds) Predation: direct and indirect impacts on aquatic communities. University Press of New England, Hanover, NH, pp 203–224

    Google Scholar 

  • Tegner MJ, Dayton PK (2000) Ecosystem effects of fishing in kelp forest communities. ICES J Mar Sci 57:579–589

    Article  Google Scholar 

  • Turingan RG, Wainwright PC (1993) Morphological and functional bases of durophagy in the queen triggerfish, Balistes vetula (Pisces, Tetraodontiformes). J Morphol 215:101–118

    Article  Google Scholar 

  • Wainwright PC, Bellwood DR (2002) Ecomorphology of feeding in coral reef fishes. In: Sale PF (ed) Coral Reef Fishes: dynamics and diversity in a complex ecosystem. Academic Press, San Diego, pp 33–55

    Google Scholar 

  • Wootton RJ (1998) Ecology of teleost fishes. Kluwer Academic Publishers, Dordrecht

    Google Scholar 

  • Young MAL, Bellwood DR (2011) Diel patterns in sea urchin activity and predation on sea urchins on the Great Barrier Reef. Coral Reefs 30:729–736

    Article  Google Scholar 

Download references

Acknowledgments

We thank the staff of the Lizard Island Research Station (an Australian Museum facility) for the provision of logistical support and facilities. Thanks also to Mike Cappo for assistance with identifications and to Ron Schroeder and Carine Lefèvre for invaluable support in the field. Financial support for the project was made available by the ARC Centre of Excellence for Coral Reef Studies.

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Correspondence to M. A. L. Young.

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Communicated by Biology Editor Dr. Stephen Swearer

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Young, M.A.L., Bellwood, D.R. Fish predation on sea urchins on the Great Barrier Reef. Coral Reefs 31, 731–738 (2012). https://doi.org/10.1007/s00338-012-0905-0

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