Coral Reefs

, Volume 35, Issue 2, pp 399–409 | Cite as

Consequences of extreme life history traits on population persistence: do short-lived gobies face demographic bottlenecks?

  • Carine D. Lefèvre
  • Kirsty L. Nash
  • Alonso González-Cabello
  • David R. Bellwood


The majority of coral reef goby species are short-lived, with some highly abundant species living less than 100 d. To understand the role and consequences of this extreme life history in shaping coral reef fish populations, we quantitatively documented the structure of small reef fish populations over a 26-month period (>14 short-lived fish generations) at an inshore reef on the Great Barrier Reef, Australia. Most species with life spans >1 yr, such as pomacentrids, exhibited a peak in recruitment during the austral summer, driving seasonal changes in the small fish community composition. In contrast, there were no clear changes in goby community composition, despite the abundance of short-lived, high turnover species. Species of Eviota, the most abundant gobiid genus observed, showed remarkably similar demographic profiles year-round, with consistent densities of adults as well as recently recruited juveniles. Our results demonstrate ongoing recruitment of these small cryptic fishes, which appears to compensate for an exceptionally short life span on the reef. Our results suggest that gobiid populations are able to overcome demographic limitations, and by maintaining reproduction, larval survival and recruitment throughout the year, they may avoid population bottlenecks. These findings also underline the potential trophodynamic importance of these small species; because of this constant turnover, Eviota species and other short-lived fishes may be particularly valuable contributors to the flow of energy on coral reefs, underpinning the year-round trophic structure.


Life history Year-round recruitment Gobiidae Short life span Coral reef trophodynamics Eviota 



We thank the staff of Orpheus Island Research Station for field support; R Bonaldo, J Hopf, V Mocellin, P Osmond, T Sunderland and J Welsh for field assistance; H Larson and R Winterbottom for taxonomic identifications; C Goatley, R Bonaldo and three anonymous reviewers for helpful discussions or comments on the earlier drafts of the manuscript. This project was supported by the Australian Research Council (DRB).

Supplementary material

338_2016_1406_MOESM1_ESM.docx (1.2 mb)
Supplementary material 1 (DOCX 1244 kb)


  1. Ackerman JL, Bellwood DR (2002) Comparative efficiency of clove oil and rotenone for sampling tropical reef fish assemblages. J Fish Biol 60:893–901CrossRefGoogle Scholar
  2. Ackerman JL, Bellwood DR (2003) The contribution of small individuals to density-body size relationships. Oecologia 136:137–140CrossRefPubMedGoogle Scholar
  3. Ackerman JL, Bellwood DR, Brown JH (2004) The contribution of small individuals to density-body size relationships: examination of energetic equivalence in reef fishes. Oecologia 139:568–571CrossRefPubMedGoogle Scholar
  4. Ahmadia GN, Pezold FL, Smith DJ (2012a) Cryptobenthic fish biodiversity and microhabitat use in healthy and degraded coral reefs in SE Sulawesi, Indonesia. Mar Biodiv 42:433–442CrossRefGoogle Scholar
  5. Ahmadia GN, Sheard LJ, Pezold FL, Smith DJ (2012b) Cryptobenthic fish assemblages across the coral reef-seagrass continuum in SE Sulawesi, Indonesia. Aquat Biol 16:125–135CrossRefGoogle Scholar
  6. Allen GR, Steene R, Humann P (2003) Reef fish identification: tropical Pacific. New World Publications, Jacksonville, FLGoogle Scholar
  7. Almany GR (2004) Does increased habitat complexity reduce predation and competition in coral reef fish assemblages? Oikos 106:275–284CrossRefGoogle Scholar
  8. Almany GR, Webster MS (2006) The predation gauntlet: early post-settlement mortality in reef fishes. Coral Reefs 25:19–22CrossRefGoogle Scholar
  9. Bellwood DR, Hoey AS, Ackerman JL, Depczynski M (2006) Coral bleaching, reef fish community phase shifts and the resilience of coral reefs. Glob Chang Biol 12:1587–1594CrossRefGoogle Scholar
  10. Bellwood DR, Baird AH, Depczynski M, González-Cabello A, Hoey AS, Lefèvre CD, Tanner JK (2012) Coral recovery may not herald the return of fishes on damaged coral reefs. Oecologia 170:567–573CrossRefPubMedGoogle Scholar
  11. Bergenius MAJ, Meekan MG, Robertson DR, McCormick MI (2002) Larval growth predicts the recruitment success of a coral reef fish. Oecologia 131:521–525CrossRefGoogle Scholar
  12. Bergenius MAJ, McCormick MI, Meekan MG, Robertson DR (2005) Environmental influences on larval duration, growth and magnitude of settlement of a coral reef fish. Mar Biol 147:291–300CrossRefGoogle Scholar
  13. Booth DJ, Brosnan DM (1995) The role of recruitment dynamics in rocky shore and coral reef fish communities. Adv Ecol Res 26:309–385CrossRefGoogle Scholar
  14. Bray RN, Miller AC, Geesey GG (1981) The fish connection: a trophic link between planktonic and rocky reef communities? Science 214:204–205CrossRefPubMedGoogle Scholar
  15. Caley MJ, Carr MH, Hixon MA, Hughes TP, Jones GP (1996) Recruitment and the local dynamics of open marine populations. Annu Rev Ecol Syst 27:477–500CrossRefGoogle Scholar
  16. Caselle JE (1999) Early post-settlement mortality in a coral reef fish and its effect on local population size. Ecol Monogr 69:177–194CrossRefGoogle Scholar
  17. Choat JH, Axe LM (1996) Growth and longevity in acanthurid fishes: an analysis of otolith increments. Mar Ecol Prog Ser 134:15–26CrossRefGoogle Scholar
  18. Clifton KE (1995) Asynchronous food availability on neighboring Caribbean coral reefs determines seasonal patterns of growth and reproduction for the herbivorous parrotfish Scarus iserti. Mar Ecol Prog Ser 116:39–46CrossRefGoogle Scholar
  19. D’Alessandro EK, Sponaugle S, Llopiz JK, Cowen RK (2011) Larval ecology of the great barracuda, Sphyraena barracuda, and other sphyraenids in the Straits of Florida. Mar Biol 158:2625–2638CrossRefGoogle Scholar
  20. De’ath G, Fabricius KE, Sweatman H, Puotinen M (2012) The 27-year decline of coral cover on the Great Barrier Reef and its causes. Proc Natl Acad Sci U S A 109:17995–17999CrossRefPubMedPubMedCentralGoogle Scholar
  21. Depczynski M, Bellwood DR (2003) The role of cryptobenthic reef fishes in coral reef trophodynamics. Mar Ecol Prog Ser 256:183–191CrossRefGoogle Scholar
  22. Depczynski M, Bellwood DR (2004) Microhabitat utilisation patterns in cryptobenthic coral reef fish communities. Mar Biol 145:455–463CrossRefGoogle Scholar
  23. Depczynski M, Bellwood DR (2005) Shortest recorded vertebrate lifespan found in a coral reef fish. Curr Biol 15:R288–R289CrossRefPubMedGoogle Scholar
  24. Depczynski M, Bellwood DR (2006) Extremes, plasticity, and invariance in vertebrate life history traits: Insights from coral reef fishes. Ecology 87:3119–3127CrossRefPubMedGoogle Scholar
  25. Depczynski M, Fulton CJ, Marnane MJ, Bellwood DR (2007) Life history patterns shape energy allocation among fishes on coral reefs. Oecologia 153:111–120CrossRefPubMedGoogle Scholar
  26. Doherty PJ (1983) Diel, lunar and seasonal rhythms in the reproduction of two tropical damselfishes: Pomacentrus flavicauda and P. wardi. Mar Biol 75:215–224CrossRefGoogle Scholar
  27. Doherty PJ (1991) Spatial and temporal patterns in recruitment. In: Sale PF (ed) The ecology of fishes on coral reefs. Academic Press, San Diego, New York, pp 261–293CrossRefGoogle Scholar
  28. Doherty PJ, Williams DM (1988) The replenishment of coral reef fish populations. Oceanogr Mar Biol Annu Rev 26:487–551Google Scholar
  29. Doherty PJ, Fowler T (1994) An empirical test of recruitment limitation in a coral reef fish. Science 263:935–939CrossRefPubMedGoogle Scholar
  30. Doherty PJ, Dufour V, Galzin R, Hixon MA, Meekan MG (2004) High mortality during settlement is a population bottleneck for a tropical surgeonfish. Ecology 85:2422–2428CrossRefGoogle Scholar
  31. Forrester GE, Steele MA (2004) Predators, prey refuges, and the spatial scaling of density-dependent prey mortality. Ecology 85:1332–1342CrossRefGoogle Scholar
  32. Forrester GE, Steele MA, Samhouri JF, Evans B, Vance RR (2008) Spatial density dependence scales up but does not produce temporal density dependence in a reef fish. Ecology 89:2980–2985CrossRefGoogle Scholar
  33. Frederick JL (1997) Post-settlement movement of coral reef fishes and bias in survival estimates. Mar Ecol Prog Ser 150:65–74CrossRefGoogle Scholar
  34. González-Cabello A, Bellwood DR (2009) Local ecological impacts of regional biodiversity on reef fish assemblages. J Biogeogr 36:1129–1137CrossRefGoogle Scholar
  35. Hamilton SL, White JW, Caselle JE, Swearer SE, Warner RR (2006) Consistent long-term spatial gradients in replenishment for an island population of a coral reef fish. Mar Ecol Prog Ser 306:247–256CrossRefGoogle Scholar
  36. Herler J, Munday PL, Hernaman V (2011) Gobies on coral reefs. In: Patzner RA, Van Tassel JL, Kovacic M, Kapoor BG (eds) The biology of gobies. Science Publishers, Boca Raton, FL, pp 493–529CrossRefGoogle Scholar
  37. Hernaman V, Munday PL (2005) Life-history characteristics of coral reef gobies. I. Growth and life-span. Mar Ecol Prog Ser 290:207–221CrossRefGoogle Scholar
  38. Hiatt RW, Strasburg DW (1960) Ecological relationships of the fish fauna on coral reefs of the Marshall Islands. Ecol Monogr 30:65–127CrossRefGoogle Scholar
  39. 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, San Diego, New York, pp 475–507CrossRefGoogle Scholar
  40. Hixon MA, Jones GP (2005) Competition, predation, and density-dependent mortality in demersal marine fishes. Ecology 86:2847–2859CrossRefGoogle Scholar
  41. Hixon MA, Anderson TW, Buch KL, Johnson DW, McLeod JB, Stallings CD (2012) Density dependence and population regulation in marine fish: a large-scale, long-term field manipulation. Ecol Monogr 82:467–489CrossRefGoogle Scholar
  42. Hughes TP, Bellwood DR, Folke C, Steneck RS, Wilson J (2005) New paradigms for supporting the resilience of marine ecosystems. Trends Ecol Evol 20:380–386CrossRefPubMedGoogle Scholar
  43. Hughes TP, Graham NA, Jackson JB, Mumby PJ, Steneck RS (2010) Rising to the challenge of sustaining coral reef resilience. Trends Ecol Evol 25:633–642CrossRefPubMedGoogle Scholar
  44. Karino K, Arai R (2006) Effect of clutch size on male egg-fanning behavior and hatching success in the goby, Eviota prasina (Klunzinger). J Exp Mar Bio Ecol 334:43–50CrossRefGoogle Scholar
  45. Kingsford MJ, Finn MD, O’Callaghan MD, Atema J, Gerlach G (2014) Planktonic larval duration, age and growth of Ostorhinchus doederleini (Pisces: Apogonidae) on the southern Great Barrier Reef, Australia. Mar Biol 161:245–259CrossRefGoogle Scholar
  46. Kramer MJ, Bellwood DR, Bellwood O (2014) Benthic Crustacea on coral reefs: a quantitative survey. Mar Ecol Prog Ser 511:105–116CrossRefGoogle Scholar
  47. Kritzer JP (2002) Stock structure, mortality and growth of the decorated goby, Istigobius decoratus (Gobiidae), at Lizard Island, Great Barrier Reef. Environ Biol Fish 63:211–216CrossRefGoogle Scholar
  48. Lachner E, Karnella S (1980) Fishes of the Indo-Pacific: genus Eviota with descriptions of eight new species (Teleostei, Gobiidae). Smithson Contrib Zool 315:1–127CrossRefGoogle Scholar
  49. Langston RC (2004) Gonad morphology and sex change in sandburrowers (Teleostei: Creediidae). Ph.D. thesis, University of Hawai’i, Honolulu, HIGoogle Scholar
  50. Lefèvre CD, Bellwood DR (2015) Disturbance and recolonisation by small reef fishes: the role of local movement versus recruitment. Mar Ecol Prog Ser 537:205–215CrossRefGoogle Scholar
  51. Longenecker K, Langston R (2005) Life history of the Hawaiian blackhead triplefin, Enneapterygius atriceps (Blennioidei, Tripterygiidae). Environ Biol Fish 73:243–251CrossRefGoogle Scholar
  52. McCormick MI (1994) Variability in age and size at settlement of the tropical goatfish Upeneus tragula (Mullidae) in the northern Great Barrier Reef lagoon. Mar Ecol Prog Ser 103:1–15CrossRefGoogle Scholar
  53. McCormick MI, Molony BW (1995) Influence of water temperature during the larval stage on size, age and body condition of a tropical reef fish at settlement. Mar Ecol Prog Ser 118:59–68CrossRefGoogle Scholar
  54. McFarland WN, Brothers EB, Ogden JC, Shulman MJ, Bermingham EL (1985) Recruitment patterns in young French grunts, Haemulon flavolineatum (Family Haemulidae), at St-Croix, Virgin Islands. Fish Bull 83:413–426Google Scholar
  55. Menge BA (2000) Recruitment vs. postrecruitment processes as determinants of barnacle population abundance. Ecol Monogr 70:265–288CrossRefGoogle Scholar
  56. Milicich MJ, Doherty PJ (1994) Larval supply of coral reef fish populations: magnitude and synchrony of replenishment to Lizard Island, Great Barrier Reef. Mar Ecol Prog Ser 110:121–134CrossRefGoogle Scholar
  57. Milicich MJ, Meekan MG, Doherty PJ (1992) Larval supply: a good predictor of recruitment of three species of reef fish (Pomacentridae). Mar Ecol Prog Ser 86:153–166CrossRefGoogle Scholar
  58. Miller PJ (1996) The functional ecology of small fish: Some opportunities and consequences. In: Miller PJ (ed) Miniature vertebrates: the implications of small body size. Oxford University Press, Oxford, pp 175–199Google Scholar
  59. Munday PL, Jones GP (1998) The ecological implications of small body size among coral-reef fishes. Oceanogr Mar Biol Annu Rev 36:373–411Google Scholar
  60. Neff BD (2003) Decisions about parental care in response to perceived paternity. Nature 422:716–719CrossRefPubMedGoogle Scholar
  61. Odum HT, Odum EP (1955) Trophic structure and productivity of a windward coral reef community on Eniwetok Atoll. Ecol Monogr 25:291–320CrossRefGoogle Scholar
  62. Randall J (2005) Reef and shore fishes of the southern Pacific: New Caledonia to Tahiti and the Pitcairn Islands. University of Hawai’i Press, Honolulu, HIGoogle Scholar
  63. Randall J, Allen G, Steene R (1997) Fishes of the Great Barrier Reef and Coral Sea, 2nd edn. University of Hawai’i Press, Honolulu, HIGoogle Scholar
  64. Robertson DR (1990) Differences in the seasonalities of spawning and recruitment of some small neotropical reef fishes. J Exp Mar Bio Ecol 144:49–62CrossRefGoogle Scholar
  65. Robertson DR (1991) The role of adult biology in the timing of spawning of tropical reef fishes. In: Sale PF (ed) The ecology of fishes on coral reefs. Academic Press, San Diego, New York, pp 356–386CrossRefGoogle Scholar
  66. Robertson DR (1992) Patterns of lunar settlement and early recruitment in Caribbean reef fishes at Panamá. Mar Biol 114:527–537CrossRefGoogle Scholar
  67. Robertson DR, Smith-Vaniz WF (2010) Use of clove oil in collecting coral reef fishes for research. Mar Ecol Prog Ser 401:295–302CrossRefGoogle Scholar
  68. Robertson DR, Schober UM, Brawn JD (1993) Comparative variation in spawning output and juvenile recruitment of some Caribbean reef fishes. Mar Ecol Prog Ser 94:105–113CrossRefGoogle Scholar
  69. Robertson DR, Swearer SE, Kaufmann K, Brothers EB (1999) Settlement vs. environmental dynamics in a pelagic-spawning reef fish at Caribbean Panama. Ecol Monogr 69:195–218CrossRefGoogle Scholar
  70. Saeki T, Sakai Y, Hashimoto H, Gushima K (2005) Foraging behavior and diet composition of Trimma caudomaculata and Trimma caesiura (Gobiidae) on coral reefs in Okinawa, Japan. Ichthyol Res 52:302–305CrossRefGoogle Scholar
  71. Sale PF (1980) The ecology of fishes on coral reefs. Oceanogr Mar Biol Annu Rev 18:367–421Google Scholar
  72. Sale PF, Douglas WA (1984) Temporal variability in the community structure of fish on coral patch reefs and the relation of community structure to reef structure. Ecology 65:409–422CrossRefGoogle Scholar
  73. Sale PF, Guy JA, Steel WJ (1994) Ecological structure of assemblages of coral reef fishes on isolated patch reefs. Oecologia 98:83–99CrossRefGoogle Scholar
  74. Searcy SP, Sponaugle S (2000) Variable larval growth in a coral reef fish. Mar Ecol Prog Ser 206:213–226CrossRefGoogle Scholar
  75. Shulman MJ, Ogden JC (1987) What controls tropical reef fish populations: recruitment or benthic mortality? An example in the Caribbean reef fish Haemulon flavolineatum. Mar Ecol Prog Ser 39:233–242CrossRefGoogle Scholar
  76. Smith C, Tyler JC (1972) Space resource sharing in a coral reef community. Bulletin of the Natural History Museum of Los Angeles City 14:125–170Google Scholar
  77. Sogard SM (1997) Size-selective mortality in the juvenile stage of teleost fishes: a review. Bull Mar Sci 60:1129–1157Google Scholar
  78. Sponaugle S (2015) Recruitment of coral reef fishes: linkages across stages. In: Mora C (ed.) Ecology of fishes on coral reefs. Cambridge University Press, pp 28–33Google Scholar
  79. Sponaugle S, Lee T, Kourafalou V, Pinkard D (2005) Florida current frontal eddies and the settlement of coral reef fishes. Limnol Oceanogr 50:1033–1048CrossRefGoogle Scholar
  80. Srinivasan M, Jones GP (2006) Extended breeding and recruitment periods of fishes on a low latitude coral reef. Coral Reefs 25:673–682CrossRefGoogle Scholar
  81. Steele MA, Forrester GE (2002) Early postsettlement predation on three reef fishes: effects on spatial patterns of recruitment. Ecology 83:1076–1091CrossRefGoogle Scholar
  82. Steele MA, Forrester GE (2005) Small-scale field experiments accurately scale up to predict density dependence in reef fish populations at large scales. Proc Natl Acad Sci U S A 102:13513–13516CrossRefPubMedPubMedCentralGoogle Scholar
  83. Sunobe T (1998) Reproductive behavior in six species of Eviota (Gobiidae) in aquaria. Ichthyol Res 45:409–412CrossRefGoogle Scholar
  84. Syms C, Jones GP (1999) Scale of disturbance and the structure of a temperate fish guild. Ecology 80:921–940CrossRefGoogle Scholar
  85. Taru M, Sunobe T (2000) Notes on reproductive ecology of the gobiid fish Eviota abax at Kominato, Japan. Bull Mar Sci 66:507–512Google Scholar
  86. Thresher RE (1984) Reproduction in reef fishes. Publications, Neptune City, New Jersey, USA, T.F.HGoogle Scholar
  87. Tornabene L, Valdez S, Erdmann M, Pezold F (2015) Support for a ‘Center of Origin’ in the Coral Triangle: cryptic diversity, recent speciation, and local endemism in a diverse lineage of reef fishes (Gobiidae: Eviota). Mol Phylogenet Evol 82:200–210CrossRefPubMedGoogle Scholar
  88. Tornabene L, Ahmadia GN, Berumen ML, Smith DJ, Jompa J, Pezold FL (2013) Evolution of microhabitat association and morphology in a diverse group of cryptobenthic coral reef fishes (Teleostei: Gobiidae: Eviota). Mol Phylogenet Evol 66:391–400CrossRefPubMedGoogle Scholar
  89. Vallès H, Kramer DL, Hunte W (2008) Temporal and spatial patterns in the recruitment of coral-reef fishes in Barbados. Mar Ecol Prog Ser 363:257–272CrossRefGoogle Scholar
  90. Vallès H, Hunte W, Kramer DL (2009) Variable temporal relationships between environment and recruitment in coral reef fishes. Mar Ecol Prog Ser 379:225–240CrossRefGoogle Scholar
  91. Victor BC (1983) Recruitment and population dynamics of a coral reef fish. Science 219:419–420CrossRefPubMedGoogle Scholar
  92. Victor BC, Vasquez-Yeomans L, Valdez-Moreno M, Wilk L, Jones DL, Lara MR, Caldow C, Shivji M (2010) The larval, juvenile, and adult stages of the Caribbean goby, Coryphopterus kuna (Teleostei: Gobiidae): a reef fish with a pelagic larval duration longer than the post-settlement lifespan. Zootaxa 2346:53–61Google Scholar
  93. Warner RR, Chesson PL (1985) Coexistence mediated by recruitment fluctuations—a field guide to the storage effect. Am Nat 125:769–787CrossRefGoogle Scholar
  94. Williams DM (1980) Dynamics of the pomacentrid community on small patch reefs in One Tree Lagoon (Great Barrier Reef). Bull Mar Sci 30:159–170Google Scholar
  95. Willis TJ, Anderson MJ (2003) Structure of cryptic reef fish assemblages: relationships with habitat characteristics and predator density. Mar Ecol Prog Ser 257:209–221CrossRefGoogle Scholar
  96. Wilson DT (2001) Patterns of replenishment of coral reef fishes in the nearshore waters of the San Blas Archipelago, Caribbean Panama. Mar Biol 139:735–753Google Scholar
  97. Wilson SK (2004) Growth, mortality and turnover rates of a small detritivorous fish. Mar Ecol Prog Ser 284:253–259CrossRefGoogle Scholar
  98. Winterbottom R, Southcott L (2008) Short lifespan and high mortality in the western Pacific coral reef goby Trimma nasa. Mar Ecol Prog Ser 366:203–208CrossRefGoogle Scholar
  99. Winterbottom R, Hoese DF (2015) A revision of the Australian species of Trimma (Actinopterygii, Gobiidae), with descriptions of six new species and redescriptions of twenty-three valid species. Zootaxa 3934:1–102CrossRefPubMedGoogle Scholar
  100. Winterbottom R, Alofs KM, Marseu A (2011) Life span, growth and mortality in the western Pacific goby Trimma benjamini, and comparisons with T. nasa. Environ Biol Fish 91:295–301CrossRefGoogle Scholar

Copyright information

© Springer-Verlag Berlin Heidelberg 2016

Authors and Affiliations

  • Carine D. Lefèvre
    • 1
    • 2
  • Kirsty L. Nash
    • 1
    • 2
  • Alonso González-Cabello
    • 1
    • 2
  • David R. Bellwood
    • 1
    • 2
  1. 1.Australian Research Council Centre of Excellence for Coral Reef StudiesJames Cook UniversityTownsvilleAustralia
  2. 2.College of Marine and Environmental SciencesJames Cook UniversityTownsvilleAustralia

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