Skip to main content

Advertisement

Log in

Contrasting patterns of reef utilization and recruitment of coral trout (Plectropomus leopardus) and snapper (Lutjanus carponotatus) at One Tree Island, southern Great Barrier Reef

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

Abstract

Patterns of abundance, age structure and recruitment of coral trout (Plectropomus leopardus) and snapper (Lutjanus carponotatus) were described in different environments, which varied in benthic cover, in a 12-yr study at One Tree Island. It was hypothesized that both taxa would show strong preferences to different environments and benthic cover and that patterns would be consistent through time. Plectropomus leopardus were abundant on the reef slope and seaward edge of the lagoon, where live coral cover was high, and recruitment was generally low, in all environments. The population was sustained by a trickle of recruits, and total abundance varied little after 10 to 25 yr of protection in a no-take area, suggesting P. leopardus had reached an environment-related carrying capacity. Protogynous P. leopardus recruited to shallow environments at sites with 20% or more hard live coral and age data indicated the abundance of fish on the reef slope was from redistribution. Most recruits of gonochoristic L. carponotatus (<150 mm Standard length, SL) were found in the lagoonal environments, and adults were rare on the reef slope. Abundance of recruit L. carponotatus and P. leopardus did not correlate with percent cover of live and soft coral within environments. Recruits of L. carponotatus were usually rare in all lagoonal environments, but in 2003, many recruits (80 to 120 mm SL) were found in lagoonal environments with low and high hard live coral cover. A substantial proportion of the population (age max 18 yr) was from strong recruitment events. In 2003 and 2004, total abundance of L. carponotatus was supported by 1 year class 51.7 and 41% respectively. The utilization of environments and types of substrata varied among taxa and in some cases among life-history stages. There was also temporal variation in the importance of some environments (e.g. Lagoon Centre).

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.

Institutional subscriptions

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8

Similar content being viewed by others

References

  • Adams S (2003) Morphological ontogeny of the gonad of three plectropomid species through sex differentiation and transition. J Fish Biol 63:22–36

    Article  Google Scholar 

  • Adams AJ, Ebersole JP (2004) Processes influencing recruitment inferred from distributions of coral reef fishes. Bull Mar Sci 75:153–174

    Google Scholar 

  • Anderson MJ, Willis TJ (2003) Canonical analysis of principal coordinates: a useful method of constrained ordination for ecology. Ecology 84:511–525

    Article  Google Scholar 

  • Booth D, Beretta G (2002) Changes in a fish assemblage after a coral bleaching event. Mar Ecol Prog Ser 245:205–212

    Article  Google Scholar 

  • Booth DJ, Kingsford MJ, Doherty PJ, Berretta GA (2000) Recruitment of damselfishes in One Tree Island lagoon: persistent interannual spatial patterns. Mar Ecol Prog Ser 202:212–230

    Article  Google Scholar 

  • Cappo M, Eden P, Newman S, Robertson S (2000) A new approach to validation of periodicity and timing of opaque zone formation in the otoliths of eleven species of Lutjanus from the central Great Barrier Reef. Fish Bull 98:474–488

    Google Scholar 

  • Caselle JE, Warner RR (1996) Variability in recruitment of coral reef fishes: the importance of habitat and two spatial scales. Ecology 77:2488–2504

    Article  Google Scholar 

  • Choat JH, Axe LM (1996) Growth and longevity in acanthurid fishes: an analysis of otolith increments. Mar Ecol Prog Ser 134:15–26

    Article  Google Scholar 

  • Connell SD (1997) The relationship between large predatory fish and recruitment and mortality of juvenile coral reef-fish on artificial reefs. J Exp Mar Biol Ecol 209:261–278

    Article  Google Scholar 

  • Connell SD (1998) Patterns of piscivory by resident predatory reef fish at One Tree Reef, Great Barrier Reef. Mar Freshw Res 49:25–30

    Article  Google Scholar 

  • Connell SD, Jones GP (1991) The influence of habitat complexity on postrecruitment processes in a temperate reef fish population. J Exp Mar Biol Ecol 151:271–294

    Article  Google Scholar 

  • Connell SD, Kingsford MJ (1998) Spatial, temporal and habitat-related variation in the abundance of large predatory fish at One Tree Island, Australia. Coral Reefs 17:49–57

    Article  Google Scholar 

  • Doherty PJ (2002) Variable replenishment and the dynamics of reef fish populations. In: Sale PF (ed) Coral reef fishes: dynamics and diversity in a complex ecosystem. Academic Press, London, pp 327–358

    Google Scholar 

  • Doherty PJ, Williams DM (1988) The replenishment of coral reef fish populations. Oceanogr Mar Biol Annu Rev 26:487–551

    Google Scholar 

  • Eggleston DB (1995) Recruitment in Nassau grouper Epinephelus striatus: post-settlement abundance, microhabitat features, and ontobenthic habitat shifts. Mar Ecol Prog Ser 124:9–22

    Article  Google Scholar 

  • Evans RD, Russ GR (2004) Larger biomass of targeted reef fish in no-take marine reserves on the Great Barrier Reef, Australia. Aquat Conserv 14:505–519

    Article  Google Scholar 

  • Ferreira BP, Russ GR (1992) Age growth and mortality of the inshore coral trout Plectropomus leopardus (Pisces: Serranidae) from the central Great Barrier Reef, Australia. Aust J Mar Freshw Res 43:429–440

    Google Scholar 

  • Ferreira BP, Russ GR (1994) Age validation and estimation of growth rate of the coral trout, Plectropomus leopardus, (Lacepede 1802) from Lizard Island, Northern Great Barrier Reef. Fish Bull 92:46–57

    Google Scholar 

  • Ferreira BP, Russ GR (1995) Population structure of the leopard coral grouper, (Plectropomus leopardus), on fished and unfished reefs off Townsville, Central Great Barrier Reef, Australia. Fish Bull 93:629–642

    Google Scholar 

  • Francis MP (1995) Spatial and seasonal variation in the abundance of juvenile snapper (Pagrus auratus) in the north-western Hauraki Gulf. NZ J Mar Freshw Res 29:565–579

    Article  Google Scholar 

  • Friedlander AM, Parrish JD, DeFelice RD (2002) Ecology of introduced snapper Lutjanus kasmira (Forsskål) in the reef fish assemblage of a Hawaiian bay. J Fish Biol 60:28–48

    Google Scholar 

  • Goeden GB (1978) A monograph of the coral trout Plectropomus leopardus (Lacepede). Qld Fish Serv Res Bull 1:1–42

    Google Scholar 

  • Hixon MA (1991) Predation as a process structuring coral-reef fish communities. In: Sale PF (ed) The ecology of fishes on coral reefs. Academic Press, London, pp 475–508

    Google Scholar 

  • Jackson JBC, 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 293:629–638

    Article  PubMed  CAS  Google Scholar 

  • Jennings S, Kaiser MJ, Reynolds JD (2001) Marine Fisheries Ecology. Blackwell Science, Oxford

    Google Scholar 

  • Jones GP (1984) Population ecology of a temperate reef fish Pseudolabrus celidotus Bloch & Schneider (Pisces: Labridae): II. Factors influencing adult density. J Exp Mar Biol Ecol 75:277–303

    Article  Google Scholar 

  • Jones GP (1991) Postrecruitment processes in the ecology of coral reef fish populations: a multifactorial perspective. In: Sale PF (ed) The Ecology of fishes on coral reefs. Academic Press, New York, pp 294–328

    Google Scholar 

  • Jones GP, McCormick MI, Srinivasan M, Eagle JV (2004) Coral decline threatens fish biodiversity in Marine Reserves. Proc Natl Acad Sci USA 101:8251–8253

    Article  PubMed  CAS  Google Scholar 

  • Kingsford MJ (1992) Spatial and temporal variation in predation on reef-fishes by coral trout (Plectropomus leopardus), Serranidae. Coral Reefs 11:193–198

    Article  Google Scholar 

  • Kingsford MJ (1998) Analytical aspects of sampling design. In: Kingsford MJ, Battershill CN (eds) Studying temperate marine environments: a handbook for ecologists. University of Canterbury Press, Christchurch, New Zealand, pp 49–83

    Google Scholar 

  • Kingsford MJ, Battershill CN (1998) Procedures for establishing a study. In: Kingsford MJ, Battershill CN (eds) Studying temperate marine environments: A handbook for ecologists. Canterbury University Press, Christchurch, New Zealand, pp 29–48

    Google Scholar 

  • Kingsford MJ, Hughes JM (2005) Patterns of growth, mortality and size of a tropical damselfish Acanthochromis polyacanthus across the continental shelf of the Great Barrier Reef. Fish Bull 103:561–573

    Google Scholar 

  • Kritzer JP (2002) Variation in the population biology of stripey bass Lutjanus carponotatus within and between two island groups on the Great Barrier Reef. Mar Ecol Prog Ser 243:191–207

    Article  Google Scholar 

  • Kritzer JP (2004) Sex-specific growth and mortality, spawning season, and female maturation of the stripey bass (Lutjanus carponotatus) on the Great Barrier Reef. Fish Bull 102:94–97

    Google Scholar 

  • McPherson G, Squire L, O’Brien J (1988) Demersal reef fish project 1984–85: Age and growth of four important reef fish species. Fisheries Research Branch Technical Report No. FRB 88/6, Cairns

  • Moe MAJ (1969) Biology of the reef grouper Epinephelus morio (Valenciennes), from the eastern Gulf of Mexico. Professional Paper Series, Florida Department of Natural Resources. Marine Research Laboratory 10:1–95

    Google Scholar 

  • Nadon M-O, Stirling G (2006) Field and simulation analyses of visual methods for sampling coral cover. Coral Reefs 25:177–185

    Article  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 Fish 46:123–138

    Article  Google Scholar 

  • Newman S, Cappo M, Williams D (2000) Age, growth and mortality of the stripey, Lutjanus carponotatus (Richardson) and the brown-stripe snapper, L. vitta (Quoy and Gaimard) from the central Great Barrier Reef, Australia. Fish Res 48:263–275

    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, Alcala AC (1996) Marine Reserves: rates and patterns of recovery and decline of large predatory fish. Ecol Appl 6:947–961

    Article  Google Scholar 

  • Russ GR, Lou DC, Ferreira BP (1995) A long-term study on population structure of the coral trout Plectropomus leopardus on reefs open and closed to fishing in the central great Barrier Reef, Australia. CRC Reef Research Centre. Technical Report No. 3. Townsville

  • Russell DJ, McDougall AJ (2005) Movement and juvenile recruitment of mangrove jack Lutjanus argentimaculatus (Forsskål), in northern Australia. Mar Freshw Res 56:465–475

    Article  Google Scholar 

  • Samoilys MA (1997) Periodicity of spawning aggregations of coral trout Plectropomus leopardus (Pisces Serranidae) on northern Great Barrier Reef. Mar Ecol Prog Ser 160:149–159

    Article  Google Scholar 

  • Schnute J (1981) A versatile growth model with statistically stable parameters. Can J Fish Aquat Sci 38:1128–1140

    Article  Google Scholar 

  • Underwood AJ, Petraitis PS (1993) Structure of intertidal assemblages in different locations: how can local processes be compared? In: Ricklefs R, Schulter D (eds) Species diversity in ecological communities. University of Chicago Press, Chicago, pp 38–51

    Google Scholar 

  • Veron JEN (2000) Corals of the world. Australian Institute of Marine Science, Townsville

    Google Scholar 

  • Warwick RM, Clarke KR (1991) A comparison of some methods for analysing changes in benthic community structure. J Mar Biol Assoc UK 71:225–244

    Article  Google Scholar 

  • Williams DM (1991) Patterns and processes in the distribution of coral reef fishes. In: Sale PF (ed) The ecology of fishes on coral reefs. Academic Press, San Diego, pp 437–474

    Google Scholar 

  • Woods AE, Ellis RC (1994) Laboratory histopathology: a complete reference. Churchilll Livingstone, Edinburgh

    Google Scholar 

  • Zeller DC, Russ GR (1998) Marine reserves: patterns of adult movement of the coral trout (Plectropomus leopardus (Serranidae)). Can J Fish Aquat Sci 55:917–924

    Article  Google Scholar 

Download references

Acknowledgements

For assistance with benthic counts I thank Ben Stewart, Julian Hughes, Dave Welch and Mark O’Callaghan and Mark, Tim Glasby and Mathew Galetto for helping with aging fish. Many thanks to Naomi Gardiner for assistance with graphics and analyses. This research was supported by multiple grants from the Australian Research Council.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to M. J. Kingsford.

Additional information

Communicated by Ecology Editor Prof. Peter Mumby.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kingsford, M.J. Contrasting patterns of reef utilization and recruitment of coral trout (Plectropomus leopardus) and snapper (Lutjanus carponotatus) at One Tree Island, southern Great Barrier Reef. Coral Reefs 28, 251–264 (2009). https://doi.org/10.1007/s00338-008-0421-4

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00338-008-0421-4

Keywords

Navigation