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The distribution and abundance of reef-associated predatory fishes on the Great Barrier Reef

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Abstract

Predatory fishes are important components of coral-reef ecosystems of the Great Barrier Reef (GBR) through both the ecological functions they perform and their high value to recreational and commercial fisheries, estimated at $30 million in 2014. However, management of GBR predatory fish populations is hampered by a lack of knowledge of their distribution and abundance, aside from that of the highly targeted coral trout (Plectropomus spp. and Variola spp.). Furthermore, there is little information on how these fishes respond to environmental stressors such as coral bleaching, outbreaks of coral-feeding starfishes (Acanthaster planci) and storms, which limits adaptive management of their populations as the frequency or severity of such natural disturbances increases under climate change. Here, we document the distribution and abundance of 48 species of reef-associated predatory fishes and assess their vulnerability to a range of natural disturbances. There were clear differences in predatory fish assemblages across the continental shelf, but many species were widespread, with few species restricted to either inshore or offshore waters. There was weak latitudinal structure with only a few species restricted to either the northern or southern GBR. On the whole, predatory fishes were surprisingly resistant to the effects of disturbance, with few clear changes in abundance or species richness following 66 documented disturbances of varying magnitudes.

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References

  • Ayling AM, Ayling AL (1992) Abundance distribution and length frequencies of a group of large piscivorous fishes, Plectropomus spp. (Pisces: Serranidae) on the Great Barrier Reef. Unpublished report to the Great Barrier Reef Marine Park Authority, Townsville, 212 pp

  • Berkelmans R, De’ath G, Kininmonth S, Skirving WJ (2004) A comparison of the 1998 and 2002 coral bleaching events on the Great Barrier Reef: spatial correlation, patterns, and predictions. Coral Reefs 23:74–83

    Article  Google Scholar 

  • Carpenter B, Gelman A, Hoffman M, Lee D, Goodrich B, Betancourt M, Brubaker MA, Guo J, Li P, Riddell A (2017) Stan: a probabilistic programming language. J Stat Softw 76:1–31

    Article  Google Scholar 

  • Carpenter S, Walker B, Anderies JM, Abel N (2001) From metaphor to measurement: resilience of what to what? Ecosystems 4:765–781

    Article  Google Scholar 

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

    Article  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

    Article  Google Scholar 

  • Currey LM, Heupel MR, Simpfendorfer CA, Williams AJ (2015) Assessing environmental correlates of fish movement on a coral reef. Coral Reefs 34:1267–1277

    Article  Google Scholar 

  • Davidson J (1997) Optimising the use of a video transect technique for the monitoring and rapid ecological assessment of tropical benthic communities. MSc Thesis, James Cook University, Townsville, Australia, 251 pp

  • De’ath G (2007) Boosted trees for ecological modeling and prediction. Ecology 88:243–251

    Article  PubMed  Google Scholar 

  • Dinesen ZD (1983) Patterns in the distribution of soft corals across the central Great Barrier Reef. Coral Reefs 1:229–236

    Article  Google Scholar 

  • Done TJ (1982) Patterns in the distribution of coral communities across the central Great Barrier Reef. Coral Reefs 1:95–107

    Article  Google Scholar 

  • Donelson JM, Munday PL, McCormick MI, Pankhurst NW, Pankhurst PM (2010) Effects of elevated water temperature and food availability on the reproductive performance of a coral reef fish. Mar Ecol Prog Ser 401:233–243

    Article  Google Scholar 

  • Drew EA (1983) Halimeda biomass, growth rates and sediment generation on reefs in the central Great Barrier Reef province. Coral Reefs 2:101–110

    Article  Google Scholar 

  • Elith J, Leathwick JR, Hastie T (2008) A working guide to boosted regression trees. J Anim Ecol 77:802–813

    Article  CAS  PubMed  Google Scholar 

  • Emslie MJ, Pratchett MS, Cheal AJ (2011) Effects of different disturbance types on butterflyfish communities of Australia’s Great Barrier Reef. Coral Reefs 30:461–471

    Article  Google Scholar 

  • Emslie MJ, Cheal AJ, Johns KA (2014) Retention of habitat complexity minimizes disassembly of reef fish communities following disturbance: a large-scale natural experiment. PLoS One 9:e105384

    Article  PubMed  PubMed Central  Google Scholar 

  • Emslie MJ, Cheal AJ, Sweatman HPA, Delean S (2008) Recovery from disturbance of coral and reef fish communities on the Great Barrier Reef, Australia. Mar Ecol Prog Ser 371:177–190

    Article  Google Scholar 

  • Emslie MJ, Pratchett MS, Cheal AJ, Osborne K (2010) Great Barrier Reef butterflyfish community structure: the role of shelf position and benthic community type. Coral Reefs 29:705–715

    Article  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 

  • Emslie MJ, Logan M, Williamson DH, Ayling AM, MacNeil MA, Ceccarelli D, Cheal AJ, Evans RD, Johns KA, Jonker MJ, Miller IR, Osborne K, Russ GR, Sweatman HPA (2015) Expectations and outcomes of reserve network performance following re-zoning of the Great Barrier Reef Marine Park. Curr Biol 25:983–992

    Article  CAS  PubMed  Google Scholar 

  • Graham NA, Wilson SK, Jennings S, Polunin NV, Bijoux JP, Robinson J (2006) Dynamic fragility of oceanic coral reef ecosystems. Proc Natl Acad Sci U S A 103:8425–8429

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Gust N, Choat JH, McCormick MI (2001) Spatial variability in reef fish distribution, abundance, size and biomass: a multi-scale analysis. Mar Ecol Prog Ser 214:237–251

    Article  Google Scholar 

  • Hammond LS, Birtles RA, Reichelt RE (1985) Holothuroid assemblages on coral reefs across the central section of the Great Barrier Reef. Proc 5th Int Coral Reef Symp 5:285–290

  • Hixon MA, Carr MH (1997) Synergistic predation, density dependence and population regulation in marine fish. Science 277:946–949

    Article  CAS  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 

  • Jackson JB, Kirby MX, Berger WH, Bjorndal KA, Botsford LW, Bourque BJ, Bradbury RH, Cooke R, Erlandson J, Estes JA, Hughes TP, Kidwell S, Lange CB, Lenihan HS, Pandolfi JM, Peterson CH, Steneck RS, Tegner MJ, Warner RR (2001) Historical overfishing and the recent collapse of coastal ecosystems. Science 293:629–637

    Article  CAS  PubMed  Google Scholar 

  • Jones GP, Ferrell DJ, Sale PF (1992) Fish feeding and dynamics of soft-sediment mollusc populations in a coral reef lagoon. Mar Ecol Prog Ser 80:175–190

    Article  Google Scholar 

  • Jonker M, Johns K, Osborne K (2008) Surveys of benthic reef communities using underwater digital photography and counts of juvenile corals. Long-term Monitoring of the Great Barrier Reef, Standard Operation Procedure Number 10, Australian Institute of Marine Science, Townsville, Australia

  • Kerry JT, Bellwood DR (2015) Do tabular corals constitute keystone structures for fishes on coral reefs? Coral Reefs 34:41–50

    Article  Google Scholar 

  • Legendre P, Gallagher ED (2001) Ecologically meaningful transformations for ordination of species data. Oecologia 129:271–280

    Article  PubMed  Google Scholar 

  • Leigh GM, Campbell AB, Lunow CP, O’Neill MF (2014) Stock assessment of the Queensland east coast common coral trout (Plectropomus leopardus) fishery. Queensland Department of Agriculture, Fisheries and Forestry, Brisbane, Queensland

    Google Scholar 

  • Mapstone BD, Davies CR, Little LR, Punt AE, Smith ADM, Pantus F, Lou DC, Williams AJ, Jones A, Ayling AM, Russ GR, McDonald AD (2004) The effects of line fishing on the Great Barrier Reef and evaluations of alternative potential management strategies. CRC Reef Research Centre Technical Report No 52. CRC Reef Research Centre, Townsville, Australia

  • McCormick MI (1995) Fish feeding on mobile benthic invertebrates: influence of spatial variability in habitat associations. Mar Biol 121:627–637

    Article  Google Scholar 

  • Miller IR, Jonker M, Coleman G (2009) Crown-of-thorns and coral surveys using the manta tow and SCUBA search techniques. Long Term Monitoring of the Great Barrier Reef Standard Operating Procedure Number 9 Edition 3. Australian Institute of Marine Science, Townsville, Australia

  • Munday PL, McCormick MI, Nilsson GE (2012) Impact of global warming and rising CO2 levels on coral reef fishes: what hope for the future? J Exp Biol 215:3865–3873

    Article  CAS  PubMed  Google Scholar 

  • Myers RA, Worm B (2005) Extinction, survival or recovery of large predatory fishes. Philos Trans R Soc Lond B Biol Sci 360:13–20

    Article  PubMed  PubMed Central  Google Scholar 

  • Newman SJ, Williams DM (1996) Variation in reef associated assemblages of the Lutjanidae and Lethrinidae at different distances offshore in the central Great Barrier Reef. Environ Biol Fishes 46:123–138

    Article  Google Scholar 

  • Newman SJ, Williams DM, Russ GR (1997) Patterns of zonation of assemblages of the Lutjanidae, Lethrinidae and Serranidae (Epinephelinae) within and among mid-shelf and outer-shelf reefs in the central Great Barrier Reef. Mar Freshw Res 48:119–128

    Article  Google Scholar 

  • Pauly D, Christensen V, Dalsgaard J, Froese R, Torres F (1998) Fishing down marine food webs. Science 279:860–863

    Article  CAS  PubMed  Google Scholar 

  • Pitcher CR, Wassenberg TJ, Cappo MC, Smith GP, Austin M, Gordon SR, Bustamante RH, Moeseneder CH, Speare PJ, Kennedy JA, Doherty PJ, Hooper JNA (2004) Dynamics of large sessile seabed fauna, important for structural fisheries habitat and biodiversity of marine ecosystems—and use of these habitats by key finfish species. Final report to Fisheries Research and Development Corporation. CSIRO Marine Research, Brisbane, Australia, 304 pp

  • Pratchett MS, Wilson SK, Baird AH (2006) Declines in the abundance of Chaetodon butterflyfishes following extensive coral depletion. J Fish Biol 69:1269–1280

    Article  Google Scholar 

  • R Core Team (2015) R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria

    Google Scholar 

  • Ridgeway G (2006) gbm: Generalized boosted regression models. R package version 1:3

    Google Scholar 

  • Rosenzweig C, Karoly D, Vicarelli M, Neofotis P, Wu Q, Casassa G, Menzel A, Root TL, Estrella N, Seguin B, Tryjanowski P, Liu C, Rawlins S, Imeson A (2008) Attributing physical and biological impacts to anthropogenic climate change. Nature 453:353–357

    Article  CAS  PubMed  Google Scholar 

  • Rue H, Martino S, Chopin N (2009) Approximate Bayesian inference for latent Gaussian models using integrated nested Laplace approximations. J R Stat Soc Series B Stat Methodol 71:319–392

    Article  Google Scholar 

  • Russ GR (1984) 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, Cheal AJ, Dolman AM, Emslie MJ, Evans RD, Miller I, Sweatman H, Williamson DH (2008) Rapid increase in fish numbers follows creation of world’s largest marine reserve network. Curr Biol 18:R514–R515

    Article  CAS  PubMed  Google Scholar 

  • Sano M, Shimizu M, Nose Y (1984) Changes in structure of coral reef fish communities by destruction of hermatypic corals: observational and experimental views. Pacific Science 38:51–79

    Google Scholar 

  • Ulstrup KE, Berkelmans R, Ralph PJ, Van Oppen MJ (2006) Variation in bleaching sensitivity of two coral species across a latitudinal gradient on the Great Barrier Reef: the role of zooxanthellae. Mar Ecol Prog Ser 314:135–148

    Article  Google Scholar 

  • Vergés A, Steinberg PD, Hay ME, Poore AG, Campbell AH, Ballesteros E, Heck KL, Booth DJ, Coleman MA, Feary DA, Figueira W (2014) The tropicalization of temperate marine ecosystems: climate-mediated changes in herbivory and community phase shifts. Proc R Soc Lond B Biol Sci 281:20140846

    Article  Google Scholar 

  • Wickham H (2009) ggplot2: elegant graphics for data analysis. Springer, New York

    Book  Google Scholar 

  • Wilkinson CR, Cheshire AC (1988) Cross shelf variations in coral reef structure and function—influences of land and ocean. Proc 6th Int Coral Reef Symp 1:227–233

  • Williams DMcB (1982) Patterns in the distribution of fish communities across the central Great Barrier Reef. Coral Reefs 1:35–43

    Article  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 DM, Russ GR (1994) Review of data on fishes of commercial and recreational fishing interest in the Great Barrier Reef, vol 1. Great Barrier Reef Marine Park Authority, Townsville, Australia

    Google Scholar 

  • Williams DMcB, Dixon P, English S (1988) Cross shelf distribution of copepods and fish larvae across the central Great Barrier Reef. Mar Biol 99:577–589

    Article  Google Scholar 

  • Wilson SK, Graham NA, Pratchett MS, Jones GP, Polunin NV (2006) Multiple disturbances and the global degradation of coral reefs: are reef fishes at risk or resilient? Glob Chang Biol 12:2220–2234

    Article  Google Scholar 

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Authors and Affiliations

  1. Australian Institute of Marine Science, PMB Number 3, Townsville Mail Centre, Townsville, 4810, Australia

    Michael J. Emslie, Alistair J. Cheal & Murray Logan

Authors
  1. Michael J. Emslie
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  2. Alistair J. Cheal
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  3. Murray Logan
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Correspondence to Michael J. Emslie.

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Communicated by Ecology Editor Dr. Alastair Harborne

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Emslie, M.J., Cheal, A.J. & Logan, M. The distribution and abundance of reef-associated predatory fishes on the Great Barrier Reef. Coral Reefs 36, 829–846 (2017). https://doi.org/10.1007/s00338-017-1573-x

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  • DOI: https://doi.org/10.1007/s00338-017-1573-x

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