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The trophic importance of algal turfs for coral reef fishes: the crustacean link

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Abstract

On coral reefs, the epilithic algal matrix (EAM) is widely recognised as an important resource for herbivorous and detritivorous fishes. In comparison, little is known of the interaction between benthic carnivores and the EAM, despite the abundance of Crustacea within the EAM. The trophic importance of the EAM to fishes was investigated in Pioneer Bay, Orpheus Island, Great Barrier Reef. Fish densities were quantified using visual and clove oil censuses, and gut content analyses conducted on abundant fish species. Crustaceans were found to be an important dietary category, contributing between 49.5 and 100 % of the gut contents, with harpacticoid copepods being the dominant component. Of the benthic carnivores, the goby Eviota zebrina was found to consume the most harpacticoids with a mean of 249 copepods m−2 day−1. This represents approximately 0.1 % of the available harpacticoid population in the EAM. In a striking comparison, herbivorous parrotfishes were estimated to consume over 12,000 harpacticoids m−2 day−1, over 27 times more than all benthic carnivores surveyed, representing approximately 5.3 % of the available harpacticoid copepod population each day. The high consumption of harpacticoid copepods by benthic carnivores and parrotfishes indicates that harpacticoids form an important trophic link between the EAM and higher trophic levels on coral reefs.

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References

  • Ackerman JL, Bellwood DR (2000) Reef fish assemblages: a re-evaluation using enclosed rotenone stations. Mar Ecol Prog Ser 206:227–237

    Article  Google Scholar 

  • Ajiboye O, Yakubu A, Adams T, Olaji E, Nwogu N (2011) A review of the use of copepods in marine fish larviculture. Rev Fish Biol Fish 21:225–246

    Article  Google Scholar 

  • Alheit J, Scheibel W (1982) Benthic harpacticoids as a food source for fish. Mar Biol 70:141–147

    Article  Google Scholar 

  • Arias-Gonzalez JE, Delesalle B, Salvat B, Galzin R (1997) Trophic functioning of the Tiahura reef sector, Moorea Island, French Polynesia. Coral Reefs 16:231–246

    Article  Google Scholar 

  • Bellwood DR (1988) Ontogenetic changes in the diet of early post-settlement Scarus species (Pices, Scaridae). J Fish Biol 33:213–219

    Article  Google Scholar 

  • Bellwood DR, Wainwright P (2001) Locomotion in labrid fishes: Implications for habitat use and cross-shelf biogeography on the Great Barrier Reef. Coral Reefs 20:139–150

    Article  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 

  • Berkström C, Jones G, McCormick M, Srinivasan M (2012) Ecological versatility and its importance for the distribution and abundance of coral reef wrasses. Mar Ecol Prog Ser 461:151–163

    Article  Google Scholar 

  • Bonaldo R, Bellwood D (2011) Spatial variation in the effects of grazing on epilithic algal turfs on the Great Barrier Reef, Australia. Coral Reefs 30:381–390

    Article  Google Scholar 

  • Bowen SH, Lutz EV, Ahlgren MO (1995) Dietary protein and energy as determinants of food quality - trophic strategies compared. Ecology 76:899–907

    Article  Google Scholar 

  • Boxshall GA, Halsey SH (2004) An introduction to copepod diversity. The Ray Society, London

    Google Scholar 

  • Carleton JH, Hamner WM (2007) The hyperbenthic plankton community: composition, distribution, and abundance in a coral reef lagoon. Mar Ecol Prog Ser 336:77–88

    Article  Google Scholar 

  • Ceccarelli DM (2007) Modification of benthic communities by territorial damselfish: a multi-species comparison. Coral Reefs 26:853–866

    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 

  • Choat JH, Clements KD (1998) Vertebrate herbivores in marine and terrestrial environments: A nutritional ecology perspective. Annu Rev Ecol Syst 29:375–403

    Article  Google Scholar 

  • Choat JH, Kingett PD (1982) The influence of fish predation on the abundance cycles of an algal turf invertebrate fauna. Oecologia 54:88–95

    Article  Google Scholar 

  • Choat JH, Axe LM, Lou DC (1996) Growth and longevity in fishes of the family Scaridae. Mar Ecol Prog Ser 145:33–41

    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 

  • Coull BC (1990) Are members of the meiofauna food for higher trophic levels? Trans Am Microsc Soc 109:233–246

    Article  Google Scholar 

  • Coull BC (1999) Role of meiofauna in estuarine soft-bottom habitats. Aust J Ecol 24:327–343

    Article  Google Scholar 

  • de Troch M, Mees J, Wakwabi E (1998) Diets of abundant fishes from beach seine catches in seagrass beds of a tropical bay (Gazi Bay, Kenya). Belg J Zool 128:135–154

    Google Scholar 

  • Denny CM, Schiel DR (2001) Feeding ecology of the banded wrasse Notolabrus fucicola (Labridae) in southern New Zealand: Prey items, seasonal differences, and ontogenetic variation. N Z J Mar Freshw Res 35:925–933

    Article  Google Scholar 

  • Depczynski M, Bellwood DR (2003) The role of cryptobenthic reef fishes in coral reef trophodynamics. Mar Ecol Prog Ser 256:183–191

    Article  Google Scholar 

  • Depczynski M, Bellwood DR (2004) Microhabitat utilisation patterns in cryptobenthic coral reef fish communities. Mar Biol 145:455–463

    Article  Google Scholar 

  • Depczynski M, Bellwood DR (2006) Extremes, plasticity, and invariance in vertebrate life history traits: Insights from coral reef fishes. Ecology 87:3119–3127

    Article  PubMed  Google Scholar 

  • Dickens LC, Goatley CHR, Tanner JK, Bellwood DR (2011) Quantifying relative diver effects in underwater visual censuses. PLoS ONE 6(4):e18965

    Article  PubMed  CAS  Google Scholar 

  • Edgar GJ, Shaw C (1995) The production and trophic ecology of shallow-water fish assemblages in southern Australia I. Species richness, size-structure and production of fishes in Western Port. Victoria. J Exp Mar Biol Ecol 194:53–81

    Article  Google Scholar 

  • Forest J, von Vaupel Klein JC (2004) The Crustacea, revised and updated from the Traite de Zoologie. Brill, Netherlands

    Google Scholar 

  • Fox RJ, Bellwood DR (2007) Quantifying herbivory across a coral reef depth gradient. Mar Ecol Prog Ser 339:49–59

    Article  Google Scholar 

  • Fox RJ, Bellwood DR (2008) Direct versus indirect methods of quantifying herbivore grazing impact on a coral reef. Mar Biol 154:325–334

    Article  Google Scholar 

  • Fricke A, Teichberg M, Beilfuss S, Bischof K (2011) Succession patterns in algal turf vegetation on a Caribbean coral reef. Bot Mar 54:111–126

    Article  Google Scholar 

  • Gee JM (1987) Impact of epibenthic predation on estuarine intertidal harpacticoid copepod populations. Mar Biol 96:497–510

    Article  Google Scholar 

  • Gee JM (1989) An ecological and economic review of meiofauna as food for fish. Zool J Linn Soc 96:243–261

    Article  Google Scholar 

  • Goatley CHR, Bellwood DR (2011) The roles of dimensionality, canopies and complexity in ecosystem monitoring. PLoS ONE 6(11):e27307

    Article  PubMed  CAS  Google Scholar 

  • Hall MO, Bell SS (1993) Meiofauna on the seagrass Thalassia testudinum: Population characteristics of harpacticoid copepods and associations with algal epiphytes. Mar Biol 116:137–146

    Article  Google Scholar 

  • Hiatt RW, Strasburg DW (1960) Ecological relationships of the fish fauna on coral reefs of the Marshall Islands. Ecol Monogr 30:65–127

    Article  Google Scholar 

  • Hicks GRF (1985) Biomass and production estimates for an estuarine meiobenthic copepod, with an instantaneous assessment of exploitation by flatfish predators N Z. J Ecol 8:125–127

    Google Scholar 

  • Hicks GRF (1988) Evolutionary implications of swimming behaviour in meiobenthic copepods. Hydrobiologia 167–168:497–504

    Article  Google Scholar 

  • Jones GP, Ferrell DJ, Sale PF (1991) Fish predation and its impact on the invertebrates of coral reefs and adjacent sediments. In: Sale PF (ed) The ecology of fishes on coral reefs. Academic Press, San Diego, pp 156–181

    Google Scholar 

  • Klumpp DW, McKinnon AD (1989) Temporal and spatial patterns in primary production of a coral-reef epilithic algal community. J Exp Mar Biol Ecol 131:1–22

    Article  Google Scholar 

  • Klumpp DW, McKinnon AD (1992) Community structure, biomass and productivity of epilithic algal communities on the Great Barrier Reef: dynamics at different spatial scales. Mar Ecol Prog Ser 86:77–89

    Article  Google Scholar 

  • Klumpp DW, McKinnon AD, Mundy CN (1988) Motile cryptofauna of a coral reef: Abundance, distribution and trophic potential. Mar Ecol Prog Ser 45:95–108

    Article  Google Scholar 

  • Kramer MJ, Bellwood DR, Bellwood O (2012) Cryptofauna of the epilithic algal matrix on an inshore coral reef, Great Barrier Reef. Coral Reefs doi:10.1007/s00338-012-0924-x

  • Logan D, Townsend KA, Townsend K, Tibbetts IR (2008) Meiofauna sediment relations in leeward slope turf algae of Heron Island reef. Hydrobiologia 610:269–276

    Article  Google Scholar 

  • Marnane MJ, Bellwood DR (1997) Marker technique for investigating gut throughput rates in coral reef fishes. Mar Biol 129:15–22

    Article  Google Scholar 

  • Montagna PA, Blanchard GF, Dinet A (1995) Effect of production and biomass of intertidal microphytobenthos on meiofaunal grazing rates. J Exp Mar Biol Ecol 185:149–165

    Article  Google Scholar 

  • Nakamura Y, Horinouchi M, Nakai T, Sano M (2003) Food habits of fishes in a seagrass bed on a fringing coral reef at Iriomote Island, southern Japan. Ichthyol Res 50:0015–0022

    Article  Google Scholar 

  • Peyrot-Clausade M (1980) Motile cryptofauna of Tulear reef flats. Mar Biol 59:43–47

    Article  Google Scholar 

  • Polunin NVC, Harmelin-Vivien M, Galzin R (1995) Contrasts in algal food processing among five herbivorous coral-reef fishes. J Fish Biol 47:455–465

    Article  Google Scholar 

  • Preston NP, Doherty PJ (1994) Cross-shelf patterns in the community structure of coral-dwelling crustacea in the central region of the Great Barrier Reef. II. Cryptofauna. Mar Ecol Prog Ser 104:27–38

    Article  Google Scholar 

  • Purcell SW, Bellwood DR (2001) Spatial patterns of epilithic algal and detrital resources on a windward coral reef. Coral Reefs 20:117–125

    Article  Google Scholar 

  • Randall J, Allen G, Steene R (1997) Fishes of the Great Barrier Reef and Coral Sea, 2nd edn. University of Hawaii Press, Honolulu

    Google Scholar 

  • Reznick D, Endler JA (1982) The impact of predation on life history evolution in Trinidadian Guppies (Poecilia reticulata). Evolution 36:160–177

    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 

  • Scott FJ, Russ GR (1987) Effects of grazing on species composition of the epilithic algal community on coral reefs of the central Great Barrier Reef. Mar Ecol Prog Ser 39:293–304

    Article  Google Scholar 

  • Stella JS, Jones GP, Pratchett MS (2010) Variation in the structure of epifaunal invertebrate assemblages among coral hosts. Coral Reefs 29:957–973

    Article  Google Scholar 

  • Toepfer CS, Fleeger JW (1995) Diet of juvenile fishes Citharichthys spilopterus, Symphurus plaguisa and Gobionellus boleosoma. Bull Mar Sci 56:238–249

    Google Scholar 

  • Vermeij MJA, van Moorselaar I, Engelhard S, Hornlein C, Vonk SM, Visser PM (2010) The effects of nutrient enrichment and herbivore abundance on the ability of turf algae to overgrow coral in the Caribbean. PLoS ONE 5(12):e14312. doi:10.1371/journal.pone.0014312

    Article  PubMed  CAS  Google Scholar 

  • Wainwright PC, Bellwood DR (2002) Ecomorphology of feeding in coral reef fishes. In: Sale PF (ed) Coral reef fishes: Dynamics and diversity in a complex system. Academic Press, San Diego, pp 33–55

    Chapter  Google Scholar 

  • Wainwright PC, Bellwood DR, Westneat MW, Grubich JR, Hoey AS (2004) A functional morphospace for the skull of labrid fishes: Patterns of diversity in a complex biomechanical system. Biol J Linn Soc 82:1–25

    Article  Google Scholar 

  • Wanders JBW (1977) The role of benthic algae in the shallow reef of Curaçao (Netherlands Antilles) III: The significance of grazing. Aquat Bot 3:357–390

    Article  Google Scholar 

  • Welsh JQ, Bellwood DR (2012) Spatial ecology of the steephead parrotfish (Chlorurus microrhinos): an evaluation using acoustic telemetry. Coral Reefs 31:55–65

    Article  Google Scholar 

  • Williams DM, 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 R, Robins DB (1982) Effects of preservation on wet weight, dry weight, nitrogen and carbon contents of Calanus helgolandicus (Crustacea: Copepoda). Mar Biol 71:271–281

    Article  Google Scholar 

  • Wilson SK (2000) Trophic status and feeding selectivity of blennies (Blenniidae: Salariini). Mar Biol 136:431–437

    Article  Google Scholar 

  • Wilson S, Bellwood DR (1997) Cryptic dietary components of territorial damselfishes (Pomacentridae, Labroidei). Mar Ecol Prog Ser 153:299–310

    Article  CAS  Google Scholar 

  • Wilson SK, Bellwood DR, Choat JH, Furnas MJ (2003) Detritus in the epilithic algal matrix and its use by coral reef fishes. Oceanogr Mar Biol Annu Rev 41:279–309

    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 

  • Wolf NG, Bermingham EB, Reaka ML (1983) Relationships between fishes and mobile benthic invertebrates on coral reefs. In: Reaka ML (ed) The ecology of deep and shallow coral reefs, vol 1., Office of Undersea ResearchRockville, Maryland, pp 69–78

    Google Scholar 

  • Zeller DC (1988) Short-term effects of territoriality of a tropical damselfish and experimental exclusion of large fishes on invertebrates in algal turfs. Mar Ecol Prog Ser 44:85–93

    Article  Google Scholar 

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Acknowledgments

We wish to thank S. Leahy, J. Welsh and staff of Orpheus Island Research Station for their support in the field; Y. Bosiger and J. Welsh for their valuable assistance processing samples; and five anonymous reviewers for constructive comments. This work was supported by the Australian Research Council (D.R.B.).

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Correspondence to M. J. Kramer.

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Kramer, M.J., Bellwood, O. & Bellwood, D.R. The trophic importance of algal turfs for coral reef fishes: the crustacean link. Coral Reefs 32, 575–583 (2013). https://doi.org/10.1007/s00338-013-1009-1

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