Skip to main content
Log in

Chronic coral consumption by butterflyfishes

  • Report
  • Published:
Coral Reefs Aims and scope Submit manuscript

Abstract

Interactions between predators and prey organisms are of fundamental importance to ecological communities. While the ecological impact that grazing predators can have in terrestrial and temperate marine systems are well established, the importance of coral grazers on tropical reefs has rarely been considered. In this study, we estimate the biomass of coral tissue consumed by four prominent species of corallivorous butterflyfishes. Sub-adult butterflyfishes (60–70 mm, 6–11 g) remove between 0.6 and 0.9 g of live coral tissue per day, while larger adults (>110 mm, ~40–50 g) remove between 1.5 and 3 g of coral tissue each day. These individual consumption rates correspond to the population of coral-feeding butterflyfishes at three exposed reef crest habitats at Lizard Island, Great Barrier Reef, consuming between 14.6 g (±2.0) and 19.6 g (±3.9) .200 m−2 day−1 of coral tissue. When standardised to the biomass of butterflyfishes present, a combined reefwide removal rate of 4.2 g (±1.2) of coral tissue is consumed per 200 m−2 kg−1 of coral-feeding butterflyfishes. The quantity of coral tissue removed by these predators is considerably larger than previously expected and indicates that coral grazers are likely to play an important role in the transfer of energy fixed by corals to higher consumers. Chronic coral consumption by butterflyfishes is expected to exact a large energetic cost upon prey corals and contribute to an increased rate of coral loss on reefs already threatened by anthropogenic pressure and ongoing climate change.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

References

  • Abramsky Z, Rosenzweig ML, Subach A (2002) The costs of apprehensive foraging. Ecology 83:1330–1340

    Article  Google Scholar 

  • Anthony KRN, Kline DI, Diaz-Pulido G, Dove S, Hoegh-Guldberg O (2008) Ocean acidification causes bleaching and productivity loss in coral reef builders. Proc Natl Acad Sci USA 105:17442–17446

    Article  CAS  PubMed  Google Scholar 

  • Avila-Sakar G, Leist LL, Stephenson AG (2003) Effects of the spatial pattern of leaf damage on growth and reproduction: nodes and branches. J Ecol 91:867–879

    Article  Google Scholar 

  • Bellwood DR, Hoey AS, Ackerman JL, Depczynski M (2006) Coral bleaching, reef fish community phase shifts and the resilience of coral reefs. Global Change Biol 12:1587–1594

    Article  Google Scholar 

  • Belsky AJ (1986) Does herbivory benefit plants? A review of the evidence. Am Nat 127:870–892

    Article  Google Scholar 

  • Belsky AJ, Carson WP, Jensen CL, Fox GA (1993) Overcompensation by plants: herbivore optimization or red herring? Evol Ecol 7:109–121

    Article  Google Scholar 

  • Berumen ML, Pratchett MS, McCormick MI (2005) Within-reef differences in diet and body condition of coral-feeding butterflyfishes (Chaetodontidae). Mar Ecol Prog Ser 287:217–227

    Article  Google Scholar 

  • Bigger DS, Marvier MA (1998) How different would a world without herbivory be? A search for generality in ecology. Integr Biol 1:60–67

    Article  Google Scholar 

  • Blumer P, Diemer M (1996) The occurrence and consequences of grasshopper herbivory in an alpine grassland, Swiss Central Alps. Arct Alp Res 28:435–440

    Article  Google Scholar 

  • Bruno JF, Stachowicz JJ, Bertness MD (2003) Inclusion of facilitation into ecological theory. Trends Ecol Evol 18:119–125

    Article  Google Scholar 

  • Carpenter SR, Kitchell JF, Hodgson JR (1985) Cascading trophic interactions and lake productivity. Bioscience 35:634–639

    Article  Google Scholar 

  • Carpenter KE, Abrar M, Aeby G, Aronson RB, Banks S, Bruckner A, Chiriboga A, Cortes J, Delbeek JC, DeVantier L, Edgar GJ, Edwards AJ, Fenner D, Guzmán HM, Hoeksema BW, Hodgson G, Johan O, Licuanan WY, Livingstone SR, Lovell ER, Moore JA, Obura DO, Ochavillo D, Polidoro BA, Precht WF, Quibilan MC, Reboton C, Richards ZT, Rogers AD, Sanciangco J, Sheppard A, Sheppard C, Smith J, Stuart S, Turak E, Veron JEN, Wallace C, Weil E, Wood E (2008) One-third of reef-building corals face elevated extinction risk from climate change and local impacts. Science 321:560–563

    Article  CAS  PubMed  Google Scholar 

  • Cole AJ, Pratchett MS, Jones GP (2008) Diversity and functional importance of coral-feeding fishes on tropical coral reefs. Fish Fish 9:286–307

    Google Scholar 

  • Cole AJ, Pratchett MS, Jones GP (2009) Effects of coral bleaching on the feeding response of two species of coral-feeding fish. J Exp Mar Biol Ecol 373:11–15

    Article  Google Scholar 

  • Costa AN, Vasconcelos HL, Vieira-Neto EHM, Bruna EM (2008) Do herbivores exert top-down effects in Neotropical savannas? Estimates of biomass consumption by leaf-cutter ants. J Veg Sci 19:849–854

    Article  Google Scholar 

  • Cox EF (1986) The effects of a selective corallivore on growth-rates and competition for space between 2 species of Hawaiian corals. J Exp Mar Biol Ecol 101:161–174

    Article  Google Scholar 

  • Cox EF (1994) Resource use by corallivorous butterflyfishes (Family Chaetodontidae) in Hawaii. Bull Mar Sci 54:535–545

    Google Scholar 

  • Crawley MJ (1997) Plant-herbivore dynamics. In: Crawley M (ed) Plant ecology vol. 2. Blackwell Scientific, Cambridge, MA, pp 401–474

    Google Scholar 

  • Emanuel K (2005) Increasing destructiveness of tropical cyclones over the past 30 years. Nature 436:686–688

    Article  CAS  PubMed  Google Scholar 

  • Glynn PW (1985) Corallivore population sizes and feeding effects following El Nino (1982–1983) associated coral mortality in Panama. Proc 5th Int Coral Reef Symp: 183–188

  • Glynn PW (1996) Coral reef bleaching: facts, hypotheses and implications. Global Change Biol 2:495–509

    Article  Google Scholar 

  • Gochfeld DJ (2010) Territorial damselfishes facilitate survival of corals by providing an associational defense against predators. Mar Ecol Pro Ser 398:137–148

    Article  Google Scholar 

  • Gregson MA, Pratchett MS, Berumen ML, Goodman BA (2008) Relationship between butterflyfish (Chaetodontidae) feeding rate and coral consumption on the Great Barrier Reef. Coral Reefs 27:583–591

    Article  Google Scholar 

  • Hall VR (2001) The response of Acropora hyacinthus and Montipora tuberculosa to three different types of colony damage: scraping injury, tissue mortality and breakage. J Exp Mar Biol Ecol 264:209–223

    Article  Google Scholar 

  • Harmelin-Vivien M, Bouchon-Navaro Y (1981) Trophic relationships among Chaetodontid fishes in the Gulf of Aquaba (Red Sea). Proc 4th Int Coral Reef Symp 2: 537–544

    Google Scholar 

  • Harmelin-Vivien ML, Bouchon-Navaro Y (1983) Feeding diets and significance of coral feeding among chaetodontid fishes in Moorea (French Polynesia). Coral Reefs 2:119–127

    Article  Google Scholar 

  • Hatcher BG (1988) Coral reef primary productivity: A beggar’s banquet. Trends Ecol Evol 3:106–111

    Article  CAS  PubMed  Google Scholar 

  • Hixon MA (1997) Effects of reef fishes on corals and algae. In: Birkeland C (ed) Life and death of coral reefs.Chapman and Hall, South Melbourne, 230–248

  • Hladun KR, Adler LS (2009) Influence of leaf herbivory, root herbivory, and pollination on plant performance in Cucurbita moschata. Ecol Entomol 34:144–152

    Article  Google Scholar 

  • Hoegh-Guldberg O, Mumby PJ, Hooten AJ, Steneck RS, Greenfield P, Gomez E, Harvell CD, Sale PF, Edwards AJ, Caldeira KN, Knowlton N, Eakin CM, Iglesias-Prieto R, Muthiga N, Bradbury RH, Dubi A, Hatziolos ME (2007) Coral reefs under rapid climate change and ocean acidification. Science 318:1737–1742

    Article  CAS  PubMed  Google Scholar 

  • Horn MH (1989) Biology of marine herbivorous fishes. Oceanogr Mar Biol Annu Rev 27:167–272

    Google Scholar 

  • Hourigan TF (1989) Environmental determinants of butterflyfish social-systems. Environ Biol Fish 25:61–78

    Article  Google Scholar 

  • Hourigan TF, Tricas TC, Reese ES (1988) Coral reef fishes as indicators of environmental stress in coral reefs. In: Soule DF, Kleppel GS (eds) Marine organisms as indicators. Springer Verlag, New York, pp 107–135

    Google Scholar 

  • Hughes TP, Baird AH, Bellwood DR, Card M, Connolly SR, Folke C, Grosberg R, Hoegh-Guldberg O, Jackson JBC, Kleypas J, Lough JM, Marshall P, Nystrom M, Palumbi SR, Pandolfi JM, Rosen B, Roughgarden J (2003) Climate change, human impacts, and the resilience of coral reefs. Science 301:929–933

    Article  CAS  PubMed  Google Scholar 

  • Idjadi JA, Edmunds PJ (2006) Scleractinian corals as facilitators for other invertebrates on a Caribbean reef. Mar Ecol Prog Ser 319:117–127

    Article  Google Scholar 

  • Ives AR, Cardinale BJ, Snyder WE (2005) A synthesis of subdisciplines: predator–prey interactions, and biodiversity and ecosystem functioning. Ecol Lett 8:102–116

    Article  Google Scholar 

  • Jayewardene D (2010) Experimental determination of the cost of lesion healing on Porites compressa growth. Coral Reefs 29:131–135

    Article  Google Scholar 

  • Jones CG, Lawton JH, Shachak M (1994) Organisms as ecosystem engineers. Oikos 69:373–386

    Article  Google Scholar 

  • Klumpp DW, Polunin NVC (1990) Algal production, grazers and habitat partitioning on a coral reef: positive correlation between grazing rate and food availability. In: Barnes M, Gibson RN (eds) Trophic relationships in the marine environment. Aberdeen University Press, Aberdeen, pp 372–388

    Google Scholar 

  • Korpinen S, Jormalainen V, Honkanen T (2007) Effects of nutrients, herbivory, and depth on the macroalgal community in the rocky sublittoral. Ecology 88:839–852

    Article  CAS  PubMed  Google Scholar 

  • Leavitt H, Robertson IC (2006) Petal herbivory by chrysomelid beetles (Phyllotreta sp.) is detrimental to pollination and seed production in Lepidium papilliferum (Brassicaceae). Ecol Entomol 31:657–660

    Article  Google Scholar 

  • Lesser MP (2007) Coral reef bleaching and global climate change: Can corals survive the next century? Proc Natl Acad Sci USA 104:5259–5260

    Article  CAS  PubMed  Google Scholar 

  • Lirman D (2000) Lesion regeneration in the branching coral Acropora palmata: effects of colonization, colony size, lesion size, and lesion shape. Mar Ecol Prog Ser 197:209–215

    Article  Google Scholar 

  • Lirman D, Fong P (1997) Patterns of damage to the branching coral Acropora palmata following Hurricane Andrew: Damage and survivorship of hurricane-generated asexual recruits. J Coast Res 13:67–72

    Google Scholar 

  • Maron JL, Crone E (2006) Herbivory: effects on plant abundance, distribution and population growth. Proc R Soc Biol Sci Ser B 273:2575–2584

    Article  Google Scholar 

  • Marshall PA, Baird AH (2000) Bleaching of corals on the Great Barrier Reef: differential susceptibilities among taxa. Coral Reefs 19:155–163

    Article  Google Scholar 

  • McNaughton SJ (1985) Ecology of a grazing ecosystem: the Serengeti. Ecol Monogr 55:259–294

    Article  Google Scholar 

  • Meyer GA (1998) Pattern of defoliation and its effect on photosynthesis and growth of goldenrod. Funct Ecol 12:270–279

    Article  Google Scholar 

  • Midoko-Iponga D, Krug CB, Milton SJ (2005) Competition and herbivory influence growth and survival of shrubs on old fields: Implications for restoration of renosterveld shrubland. J Veg Sci 16:685–692

    Article  Google Scholar 

  • Montgomery WL, Myrberg AA Jr, Fishelson L (1989) Feeding ecology of surgeonfishes (Acanthuridae) in the northern Red Sea, with particular reference to Acanthurus nigrofuscus (Forsskål). J Exp Mar Biol Ecol 132:179–207

    Article  Google Scholar 

  • Mutshinda CM, O’Hara RB, Woiwod IP (2009) What drives community dynamics? Proc R Soc Biol Sci Ser B 276:2923–2929

    Article  Google Scholar 

  • Neudecker S (1979) Effects of grazing and browsing fishes on the zonation of corals in Guam. Ecology 60:666–672

    Article  Google Scholar 

  • Oren U, Benayahu Y, Lubinevsky H, Loya Y (2001) Colony integration during regeneration in the stony coral Favia favus. Ecology 82:802–813

    Google Scholar 

  • Page C, Willis B (2006) Distribution, host range and large-scale spatial variability in black band disease prevalence on the Great Barrier Reef, Australia. Dis Aquat Org 69:41–51

    Article  PubMed  Google Scholar 

  • Pandolfi JM, Bradbury RH, Sala E, Hughes TP, Bjorndal KA, Cooke RG, McArdle D, McClenachan L, Newman MJH, Paredes G, Warner RR, Jackson JB (2003) Global trajectories of the long-term decline of coral reef ecosystems. Science 301:955–958

    Article  CAS  PubMed  Google Scholar 

  • Pitcher TJ, Lang SH, Turner JA (1988) A risk-balancing trade off between foraging rewards and predation hazard in a shoaling fish. Behav Ecol Sociobiol 22:225–228

    Article  Google Scholar 

  • Pratchett MS (2005) Dietary overlap among coral-feeding butterflyfishes (Chaetodontidae) at Lizard Island, northern Great Barrier Reef. Mar Biol 148:373–382

    Article  Google Scholar 

  • Pratchett MS (2007) Dietary selection by coral-feeding butterflyfishes (Chaetodontidae) on the Great Barrier Reef, Australia. Raffles Bull Zool 14:155–160

    Google Scholar 

  • Pratchett MS, Berumen ML (2008) Interspecific variation in distributions and diets of coral reef butterflyfishes (Teleostei: Chaetodontidae). J Fish Biol 73:1730–1747

    Article  Google Scholar 

  • Pratchett MS, Schenk TJ, Baine M, Syms C, Baird AH (2009) Selective coral mortality associated with outbreaks of Acanthaster planci L. in Bootless Bay, Papua New Guinea. Mar Environ Res 67:230–236

    Article  CAS  PubMed  Google Scholar 

  • Preisser EL, Bolnick DI, Benard MF (2005) Scared to death? The effects of intimidation and consumption in predator-prey interactions. Ecology 86:501–509

    Article  Google Scholar 

  • Reese ER (1977) Coevolution of corals and coral feeding fishes of the family Chaetodontidae. Proc 3rd Int Coral Reef Symp: 268–274

  • Ritchie ME, Tilman D, Knops JMH (1998) Herbivore effects on plant and nitrogen dynamics in oak savanna. Ecology 79:165–177

    Article  Google Scholar 

  • Roberts CM, Ormond RFG (1992) Butterflyfish social-behavior, with special reference to the incidence of territoriality: A review. Environ Biol Fish 34:79–93

    Article  Google Scholar 

  • Robertson R (1970) Review of the predators and parasites of stony corals, with special reference to symbiotic prosobranch gastropods. Pac Sci 24:43–54

    Google Scholar 

  • Rodrigues LJ, Grottoli AG (2007) Energy reserves and metabolism as indicators of coral recovery from bleaching. Limnol Oceanogr 52:1874–1882

    Article  Google Scholar 

  • Rotjan RD, Lewis SM (2008) Impact of coral predators on tropical reefs. Mar Ecol Prog Ser 367:73–91

    Article  Google Scholar 

  • Rudgers JA, Whitney KD (2006) Interactions between insect herbivores and a plant architectural dimorphism. J Ecol 94:1249–1260

    Article  Google Scholar 

  • Russ GR (2003) Grazer biomass correlates more strongly with production than with biomass of algal turfs on a coral reef. Coral Reefs 22:63–67

    Google Scholar 

  • Sano M, Shimizu M, Nose Y (1987) Long-term effects of destruction of hermatypic corals by Acanthaster planci infestation on reef fish communities at Iromote Island, Japan. Mar Ecol Pro Ser 37:191–199

    Article  Google Scholar 

  • Schmitz OJ (2007) Predator diversity and trophic interactions. Ecology 88:2415–2426

    Article  PubMed  Google Scholar 

  • Schmitz OJ, Beckerman AP, O’Brien KM (1997) Behaviorally mediated trophic cascades: effects of predation risk on food web interactions. Ecology 78:1388–1399

    Article  Google Scholar 

  • Scrimgeour GJ, Culp JM (1994) Foraging and evading predators: the effect of predator species on a behavioural trade-off by a lotic mayfly. Oikos 69:71–79

    Article  Google Scholar 

  • Steneck RS, Graham MH, Bourque BJ, Corbett D, Erlandson JM, Estes JA, Tegner MJ (2002) Kelp forest ecosystems: biodiversity, stability, resilience and future. Environ Conserv 29:436–459

    Google Scholar 

  • Thompson AA, Dolman AM (2010) Coral bleaching: one disturbance too many for near-shore reefs of the Great Barrier Reef. Coral Reefs 29:637–648

    Article  Google Scholar 

  • Titlyanov EA, Titlyanova TV, Yakovleva IM, Nakano Y, Bhagooli R (2005) Regeneration of artificial injuries on scleractinian corals and coral/algal competition for newly formed substrate. J Exp Mar Biol Ecol 323:27–42

    Article  Google Scholar 

  • Tricas TC (1989) Prey selection by coral-feeding butterflyfishes: strategies to maximize profit. Environ Biol Fish 25:171–185

    Article  Google Scholar 

  • Van Veghel MLJ, Bak RPM (1994) Reproductive characteristics of the polymorphic Caribbean reef building coral, Montastrea annularis. III. Reproduction in damaged and regenerating colonies. Mar Ecol Prog Ser 109:229–233

    Article  Google Scholar 

  • Verges A, Perez M, Alcoverro T, Romero J (2008) Compensation and resistance to herbivory in seagrasses: induced responses to simulated consumption by fish. Oecologia 155:751–760

    Article  PubMed  Google Scholar 

  • Veron JEN, Hoegh-Guldberg O, Lenton TM, Lough JM, Obura DO, Pearce-Kelly P, Sheppard CRC, Spalding M, Stafford-Smith MG, Rogers AD (2009) The coral reef crisis: The critical importance of <350 ppm CO2. Mar Pollut Bull 58:1428–1436

    Article  CAS  PubMed  Google Scholar 

  • Ward S (1995) The effect of damage on the growth, reproduction and storage of lipids in the scleractinian coral Pocillopora damicornis (Linnaeus). J Exp Mar Biol Ecol 187:193–206

    Article  CAS  Google Scholar 

  • Wellington GM (1982) Depth zonation of corals in the Gulf of Panama: control and facilitation by resident reef fishes. Ecol Monogr 52:223–241

    Article  Google Scholar 

  • Wisdom CS, Crawford CS, Aldon EF (1989) Influence of insect herbivory on photosynthetic area and reproduction in Gutierrezia species. J Ecol 77:685–692

    Article  Google Scholar 

  • Zangerl AR, Hamiliton JG, Miller TJ, Crofts AR, Oxborough K, Berenbaum MR, de Lucia EH (2002) Impact of folivory on photosynthesis is greater than the sum of its holes. Proc Natl Acad Sci USA 99:1088–1091

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

This work was funded by the ARC CoE for Coral Reef studies and a AWPS grant awarded to A. Cole. We thank K. Chong-Seng, J. Hines, D. McCowan and D. Coker for field assistance and the staff at Lizard Island Research Station for invaluable logistical advice. This paper benefited from comments provided by N. Graham,T. Petray and three anonymous reviewers. This project was covered by the JCU Animal ethics review committee no. A1306.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to A. J. Cole.

Additional information

Communicated by Biology Editor Prof. Philip Munday

Rights and permissions

Reprints and permissions

About this article

Cite this article

Cole, A.J., Lawton, R.J., Pratchett, M.S. et al. Chronic coral consumption by butterflyfishes. Coral Reefs 30, 85–93 (2011). https://doi.org/10.1007/s00338-010-0674-6

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00338-010-0674-6

Keywords

Navigation