Skip to main content

Advertisement

Log in

Diet and cross-shelf distribution of rabbitfishes (f. Siganidae) on the northern Great Barrier Reef: implications for ecosystem function

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

Abstract

Herbivorous fishes are a critical functional group on coral reefs, and there is a clear need to understand the role and relative importance of individual species in reef processes. While numerous studies have quantified the roles of parrotfishes and surgeonfishes on coral reefs, the rabbitfishes (f. Siganidae) have been largely overlooked. Consequently, they are typically viewed as a uniform group of grazing or browsing fishes. Here, we quantify the diet and distribution of rabbitfish assemblages on six reefs spanning the continental shelf in the northern Great Barrier Reef. Our results revealed marked variation in the diet and distribution of rabbitfish species. Analysis of stomach contents identified four distinct groups: browsers of leathery brown macroalgae (Siganus canaliculatus, S. javus), croppers of red and green macroalgae (S. argenteus, S. corallinus, S. doliatus, S. spinus) and mixed feeders of diverse algal material, cyanobacteria, detritus and sediment (S. lineatus, S. punctatissimus, S. punctatus, S. vulpinus). Surprisingly, the diet of the fourth group (S. puellus) contained very little algal material (22.5 %) and was instead dominated by sponges (69.1 %). Together with this variation in diet, the distribution of rabbitfishes displayed clear cross-shelf variation. Biomass was greatest on inner-shelf reefs (112.7 ± 18.2 kg.ha−1), decreasing markedly on mid- (37.8 ± 4.6 kg.ha−1) and outer-shelf reefs (9.7 ± 2.2 kg.ha−1). This pattern was largely driven by the browsing S. canaliculatus that accounted for 50 % of the biomass on inner-shelf reefs, but was absent in mid- and outer-shelf reefs. Mixed feeders, although primarily restricted to the reef slope and back reef habitats, also decreased in abundance and biomass from inshore to offshore, while algal cropping taxa were the dominant group on mid-shelf reefs. These results clearly demonstrate the extent to which diet and distribution vary within the Siganidae and emphasise the importance of examining function on a species-by-species basis.

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
Fig. 4
Fig. 5

References

  • Bellwood DR, Choat JH (1990) A functional analysis of grazing in parrotfishes (family Scaridae): the ecological implications. Environ Biol Fish 28:189–214

    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 

  • Bellwood DR, Hughes TP, Hoey AS (2006) Sleeping functional group drives coral-reef recovery. Curr Biol 16:2434–2439

    Article  PubMed  CAS  Google Scholar 

  • Bennett S, Bellwood DR (2011) Latitudinal variation in macroalgal consumption by fishes on the Great Barrier Reef. Mar Ecol Prog Ser 426:241–252

    Article  Google Scholar 

  • Borsa P, Lemer S, Aurelle D (2007) Patterns of lineage diversification in rabbitfishes. Mol Phylogenet Evol 44:427–435

    Article  PubMed  CAS  Google Scholar 

  • Brandl SJ, Bellwood DR (2013) Morphology, sociality, and ecology: can morphology predict pairing behaviour in coral reefs fishes? Coral Reefs. doi:10.1007/s00338-013-1042-0

    Google Scholar 

  • Bruggemann JH, Kuyper MWM, Breeman AM (1994) Comparative analysis of foraging and habitat use by the sympatric Caribbean parrotfish Scarus vetula and Sparisoma viride (Scaridae). Mar Ecol Prog Ser 112:51–66

    Article  Google Scholar 

  • Burkepile DE, Hay ME (2008) Herbivore species richness and feeding complementarity affect community structure and function on a coral reef. Proc Natl Acad Sci USA 105:16201–16206

    Article  PubMed  CAS  Google Scholar 

  • Burkepile DE, Hay ME (2011) Feeding complementarity versus redundancy among herbivorous fishes on a Caribbean reef. Coral Reefs 30:351–362

    Article  Google Scholar 

  • Capper A, Tibbetts IR, O’Neil JM, Shaw GR (2006) Feeding preference and deterrence in rabbitfish Siganus fuscescens for the cyanobacterium Lyngbya majuscula in Moreton Bay, south-east Queensland, Australia. J Fish Biol 68:1589–1609

    Article  Google Scholar 

  • Cheal AJ, MacNeil MA, Cripps E, Emslie MJ, Jonker M, Schaffelke B, Sweatman H (2010) Coral-macroalgal phase shifts or reef resilience: links with diversity and functional roles of herbivorous fishes on the Great Barrier Reef. Coral Reefs 29:1005–1015

    Article  Google Scholar 

  • Cheal A, Emslie M, Miller I, Sweatman S (2012) The distribution of herbivorous fishes on the Great Barrier Reef. Mar Biol 159:1143–1154

    Article  Google Scholar 

  • Choat JH, Clements KD, Robbins WD (2002) The trophic status of herbivorous fishes on coral reefs. I. Dietary analyses. Mar Biol 140:613–623

    Article  CAS  Google Scholar 

  • Choat JH, Robbins WD, Clements KD (2004) The trophic status of herbivorous fishes on coral reefs. II. Food processing modes and trophodynamics. Mar Biol 145:445–454

    Article  Google Scholar 

  • Cvitanovic C, Bellwood DR (2009) Local variation in herbivore feeding activity on an inshore reef of the Great Barrier Reef. Coral Reefs 28:127–133

    Article  Google Scholar 

  • Done TJ, Ogden JC, Wiebe WJ, Rosen BR (1996) Biodiversity and ecosystem function on coral reefs. In: Mooney HA, Cushman JH, Medina E, Sala OE, Schultze ED (eds) Functional roles of biodiversity: a global perspective. Wiley, Chichester, pp 393–429

    Google Scholar 

  • Emslie MJ, Logan M, Ceccarelli DM, Cheal AJ, Hoey AS, Miller I, Sweatman HPA (2012) Regional-scale variation in the distribution and abundance of farming damselfishes on Australia’s Great Barrier Reef. Mar Biol 159:1293–1304

    Article  Google Scholar 

  • Ferreira CEL, Peret AC, Coutinho (1998) Seasonal grazing rates and food processing by tropical herbivorous fishes. J Fish Biol 53:222–235

    Google Scholar 

  • Floeter SR, Behrens MD, Ferreira CEL, Paddack MJ, Horn MH (2005) Geographical gradients of marine herbivorous fishes: patterns and processes. Mar Biol 147:1435–1447

    Article  Google Scholar 

  • Fox RJ, Bellwood DR (2008) Remote video bioassays reveal the potential feeding impact of the rabbitfish Siganus canaliculatus (f. Siganidae) on an inner-shelf reef on the Great Barrier Reef. Coral Reefs 27:605–615

    Article  Google Scholar 

  • Fox RJ, Bellwood DR (2013) Niche partitioning of feeding microhabitats produces a unique function for herbivorous rabbitfishes (Perciformes, Siganidae) on coral reefs. Coral Reefs 32:13–23

    Article  Google Scholar 

  • Fox RJ, Sunderland TL, Hoey AS, Bellwood DR (2009) Estimating functional roles in coral reef ecosystems: behaviour drives contrasting roles in herbivorous fishes (F: Siganidae). Mar Ecol Prog Ser 385:261–269

    Article  Google Scholar 

  • Goatley CHR, Bellwood DR (2012) Sediment suppresses herbivory across a coral reef depth gradient. Biol Lett 8:1016–1018

    Article  PubMed  Google Scholar 

  • Green AL, Bellwood DR (2009) Monitoring functional groups of herbivorous reef fishes as indicators of coral reef resilience. IUCN working group on Climate Change and Coral Reefs. IUCN, Gland, Switzerland

    Google Scholar 

  • Hiroyuki M, Toshiharu T, Yoshitsugu H, Shiro N, Hisashi M, Shunsuke H, Yasuhiko N (2000) Decline of afforested Ecklonia cava community by grazing of herbivorous fish Siganus fuscescens. Fish Eng 37:135–142

    Google Scholar 

  • Hoey AS, Bellwood DR (2008) Cross-shelf variation in the role of parrotfishes on the Great Barrier Reef. Coral Reefs 27:37–47

    Article  Google Scholar 

  • Hoey AS, Bellwood DR (2009) Limited functional redundancy in a high diversity system: single species dominates key ecological process on coral reefs. Ecosystems 12:1316–1328

    Article  Google Scholar 

  • Hoey AS, Bellwood DR (2010a) Among habitat variation in herbivory on Sargassum spp. on a mid-shelf reef in the northern Great Barrier Reef. Mar Biol 157:189–200

    Article  Google Scholar 

  • Hoey AS, Bellwood DR (2010b) Cross-shelf variation in browsing intensity on the Great Barrier Reef. Coral Reefs 29:499–508

    Article  Google Scholar 

  • Hoey AS, Bellwood DR (2011) Suppression of herbivory by macroalgal density: a critical feedback on coral reefs? Ecol Lett 14:267–273

    Article  PubMed  Google Scholar 

  • Hoey AS, Pratchett MS, Cvitanovic C (2011) High macroalgal cover and low coral recruitment undermines the potential resilience of the world’s southernmost coral reef assemblage. PLoS ONE 6:e25824

    Article  PubMed  CAS  Google Scholar 

  • Hughes TP, Rodrigues MJ, Bellwood DR, Ceccarelli D, Hoegh-Guldberg O, McCook L, Moltschaniwskyj N, Pratchett MS, Steneck RS, Willis B (2007) Phase shifts, herbivory, and the resilience of coral reefs to climate change. Curr Biol 17:360–365

    Article  PubMed  CAS  Google Scholar 

  • Krone R, Bshary R, Paster M, Eisinger M, van Treeck P, Schuhmacher H (2008) Defecation behaviour of the lined bristletooth surgeonfish Ctenochaetus striatus (Acanthuridae). Coral Reefs 27:619–622

    Article  Google Scholar 

  • Kuriiwa K, Hanzawa N, Yoshino T, Kimura S, Nishida M (2007) Phylogenetic relationships and natural hybridization in rabbitfishes (Teleostei: Siganidae) inferred from mitochondrial and nuclear DNA analyses. Mol Phylogenet Evol 45:69–80

    Article  PubMed  CAS  Google Scholar 

  • Lundberg B, Golani D (1995) Diet adaptations of lessepsian migrant rabbitfishes, Siganus luridus and S. rivulatus, to the algal resources of the Mediterranean coast of Israel. Mar Ecol 16:73–89

    Article  Google Scholar 

  • Lundberg B, Lipkin Y (1979) Natural food of the herbivorous rabbitfish (Siganus spp.) in the northern Red Sea. Bot Mar 22:173–181

    Article  Google Scholar 

  • Mantyka CS, Bellwood DR (2007) Direct evaluation of macroalgal removal by herbivorous coral reef fishes. Coral Reefs 26:435–442

    Article  Google Scholar 

  • Mumby PJ, Steneck RS (2008) Coral reef management and conservation in light of rapidly evolving ecological paradigms. Trends Ecol Evol 23:555–563

    Article  PubMed  Google Scholar 

  • Nystrom M (2006) Redundancy and response diversity of functional groups: implications for the resilience of coral reefs. Ambio 35:30–35

    PubMed  Google Scholar 

  • Paul VJ, Nelson SG, Sanger HR (1990) Feeding preferences of adult and juvenile rabbitfish Siganus argenteus in relation to chemical defenses of tropical seaweeds. Mar Ecol Prog Ser 60:23–34

    Article  CAS  Google Scholar 

  • Paul VJ, Meyer KD, Nelson SG, Sanger HR (1992) Deterrent effects of seaweed extracts and secondary metabolites on feeding by the rabbitfish Siganus spinus. Proc 7th Int Coral Reef Symp 2:867–874

    Google Scholar 

  • Polunin NVC, Klumpp DW (1992) Algal food supply and grazer demand in a very productive coral-reef zone. J Exp Mar Biol Ecol 164:1–15

    Article  Google Scholar 

  • Randall JE, Allen GR, Steene RC (1997) Fishes of the Great Barrier Reef and Coral Sea. Crawford House Publishing, Bathurst

    Google Scholar 

  • Rasher DB, Hay ME (2010) Chemically rich seaweeds poison corals when not controlled by herbivores. Proc Natl Acad Sci USA 107:9683–9688

    Article  PubMed  CAS  Google Scholar 

  • Rasher DB, Hoey AS, Hay ME (2013) Consumer diversity interacts with prey defences to drive ecosystem function. Ecology. doi:10.1890/12-0389.1

    PubMed  Google Scholar 

  • Robertson DR (1982) Fish feces as fish food on a Pacific coral reef. Mar Ecol Prog Ser 7:253–265

    Article  Google Scholar 

  • Russ GR (1984a) Distribution and abundance of herbivorous grazing fishes in the central Great Barrier Reef. I. Levels of variability across the entire continental shelf. Mar Ecol Prog Ser 20:23–34

    Article  Google Scholar 

  • Russ GR (1984b) Distribution and abundance of herbivorous grazing fishes in the central Great Barrier Reef. II. Patterns of zonation of mid-shelf and outershelf reefs. Mar Ecol Prog Ser 20:35–44

    Article  Google Scholar 

  • Steneck RS (1988) Herbivory on coral reefs: a synthesis. Proc 6th Int Coral Reef Symp 1:37–49

    Google Scholar 

  • Tsuda RT, Bryan PG (1973) Food preferences of juvenile Siganus rostratus and S. spinus in Guam. Copeia 1973:604–606

    Article  Google Scholar 

  • Verges A, Vanderklift MA, Doropoulos C, Hyndes GA (2010) Spatial patterns in herbivory on a coral reef are influenced by structural complexity but not algal traits. PLoS ONE 6:e17115

    Article  Google Scholar 

  • Verges A, Bennett S, Bellwood DR (2012) Diversity among macroalgae-consuming fishes on coral reefs: a transcontinental comparison. PLoS ONE 7:e45543

    Article  PubMed  CAS  Google Scholar 

  • Williams DMcB, Hatcher AI (1983) Structure of fish communities on outer slopes of inshore, mid-shelf and outer shelf reefs of the Great Barrier Reef. Mar Ecol Prog Ser 10:239–250

    Article  Google Scholar 

  • Williams ID, Polunin NVC (2001) Large-scale associations between macroalgal cover and grazer biomass on mid-depth reefs in the Caribbean. Coral Reefs 19:358–366

    Google Scholar 

  • Wilson SK, Depczynski M, Fisher R, Holmes TH, O’Leary R, Timkler P (2010) Habitat associations of juvenile fish at Ningaloo Reef, Western reef, Western Australia: the importance of coral and algae. PLoS ONE 5:e15185

    Article  PubMed  Google Scholar 

  • Wismer S, Hoey AS, Bellwood DR (2009) Cross-shelf benthic community structure on the Great Barrier Reef: relationships between macroalgal cover and herbivore biomass. Mar Ecol Prog Ser 376:45–54

    Article  Google Scholar 

  • Woodland DJ (1990) Revision of the fish family Siganidae with descriptions of two new species and comments on distribution and biology. Indo-Pacific Fishes, No. 19. Bishop Museum, Honolulu, Hawaii

Download references

Acknowledgments

We thank J. Hoey, C. Lefevre, T. Sunderland and P. Wulf for assistance in the field. Comments by J. Hoey, S. Swearer, K. Clements and an anonymous reviewer greatly improved the manuscript. We thank the staff at the Lizard Island Research Station, a facility of the Australian Museum, for invaluable field support. Financial support was provided by The Ian Potter Doctoral Fellowship at Lizard Island (ASH) and the Australian Research Council (ASH, DRB). Research was conducted under GBRMPA permit G07/23636.1.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to A. S. Hoey.

Additional information

Communicated by Biology Editor Dr. Stephen Swearer

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (DOC 2308 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hoey, A.S., Brandl, S.J. & Bellwood, D.R. Diet and cross-shelf distribution of rabbitfishes (f. Siganidae) on the northern Great Barrier Reef: implications for ecosystem function. Coral Reefs 32, 973–984 (2013). https://doi.org/10.1007/s00338-013-1043-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00338-013-1043-z

Keywords

Navigation