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Geographical gradients of marine herbivorous fishes: patterns and processes

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Abstract

We present new data and the first rigorous analysis of latitudinal and thermal gradients of diversity, density and biomass of marine herbivorous fishes and review proposed explanatory mechanisms. Consistently, negative relationships between latitude, and positive relationships between sea surface temperature (SST), and relative richness and relative abundance of herbivorous fishes were found worldwide. Significant differences in the strength of gradients of richness and abundance with latitude and SST between tropical and extratropical zones were found consistently across ocean basins. Standardized sampling along the western Atlantic also showed negative relationships between latitude and total density and biomass. The trends, however, are driven by different components of the fish assemblages (i.e., scarids in the Caribbean and acanthurids in Brazil). Patterns of abundance along thermal gradients, generally associated with extensive latitudinal gradients, also were found at the local scale. Feeding rate of the ocean surgeonfish Acanthurus bahianus decreases with temperature more rapidly than the mean metabolic rate of teleost fishes. This relationship suggests a temperature-related physiological constraint. From the new standardized and comparative data presented and the review of the explanatory hypotheses, we conclude that temperature-related feeding and digestive processes are most likely involved in the distribution patterns of herbivorous fishes.

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References

  • Andrew NL (1989) Contrasting ecological implications of food limitation in sea urchins and herbivorous gastropods. Mar Ecol Prog Ser 51:189–193

    Article  Google Scholar 

  • Arrington DA, Winemiller KO, Loftus WF, Akin S (2002) How often do fishes “run on empty”? Ecology 83:2145–2151

    Google Scholar 

  • Barry JP, Ehret MJ (1993) Diet, food preference, and algal availability for fishes and crabs on intertidal reef communities in southern California. Envir Biol Fish 37:75–95

    Article  Google Scholar 

  • Bellwood DR (1994) A phylogenetic study of the parrotfishes family Scaridae (Pisces: Labroidei), with a revision of genera. Rec Aust Mus Suppl 20:1–86

    Google Scholar 

  • Bellwood DR (2003) Origins and escalation of herbivory in fishes: a functional perspective. Paleobiology 29:71–83

    Article  Google Scholar 

  • Bolser RC, Hay ME (1996) Are tropical plants better defended? Palatability and defenses of temperate vs. tropical seaweeds. Ecology 77:2269–2286

    Article  Google Scholar 

  • Brown JH, Lomolino MV (1998) Biogeography, 2nd edn. Sinauer Associates, Sunderland

    Google Scholar 

  • Bruggemann JH (1994) Parrotfish grazing on coral reefs: a trophic novelty. PhD Thesis, University of Groningen, Netherlands

  • CARICOMP (2002) The Caribbean coastal marine productivity program (CARCOMP) database: potential for data mining and comparisons of Caribbean-wide datasets. In: Proceedings of the 9th international coral reef symposium, 2:901–908

  • Carpenter RC (1986) Partitioning herbivory and its effects on coral reef algal communities. Ecol Monogr 56:345–363

    Article  Google Scholar 

  • Cebrian J (2002) Variability and control of carbon consumption, export, and accumulation in marine communities. Limnol Oceanogr 47:11–22

    CAS  Google Scholar 

  • Chan AS, Horn MH, Dickson KA, Gawlicka A (2004) Digestive enzyme activities in carnivores and herbivores: comparisons among four closely related prickleback fishes (Teleostei: Stichaeidae) from a California rocky intertidal habitat. J Fish Biol 65:848–858

    Article  CAS  Google Scholar 

  • Choat JH (1991) The biology of herbivorous fishes on coral reefs. In: Sale PF (ed) The ecology of fishes on coral reefs. Academic, San Diego, pp 120–155

    Google Scholar 

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

    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 

  • Clarke A, Johnston NM (1999) Scaling of metabolic rate with body mass and temperature in teleost fish. J Animal Ecol 68:893–905

    Article  Google Scholar 

  • Clements KD, Alfaro ME, Fessler JL, Westneat MW (2004) Relationships of the temperate Australasian labrid fish tribe Odacini (Perciformes; Teleostei). Mol Phylogenet Evol 32:575–587

    Article  PubMed  CAS  Google Scholar 

  • Coley PD, Aide TM (1991) A comparison of herbivory and plant defenses in temperate and tropical broad-leaved trees. In: Price PW, Lewinsohn TM, Fernandes GW, Benson WW (eds) Plant–animal interactions: evolutionary ecology in tropical and temperate regions. Wiley, New York, pp 25–49

    Google Scholar 

  • Coley PD, Barone JA (1996) Herbivory and plant defenses in tropical forests. Annu Rev Ecol Syst 27:305–335

    Article  Google Scholar 

  • Cooper WE, Vitt LJ (2002) Distribution, extent, and evolution of plant consumption by lizards. J Zool 257:487–517

    Article  Google Scholar 

  • Cossins AR, Bowler K (1987) Temperature biology of animals. Chapman and Hall, London

    Google Scholar 

  • Cronin G, Paul VJ, Hay ME, Fenical W (1997) Are tropical herbivores more resistant than temperate herbivores to seaweed chemical defenses? Diterpenoid metabolites from Dictyota acutiloba as feeding deterrents for tropical versus temperate fishes and urchins. J Chem Ecol 23:289–302

    Article  CAS  Google Scholar 

  • Crossman DJ, Choat JH, Clements KD, Hardy J, McConochie J (2001) Detritus as food for grazing fishes on coral reefs. Limnol Oceanogr 46:1596–1605

    Article  Google Scholar 

  • Cyr H, Pace ML (1993) Magnitude and patterns of herbivory in aquatic and terrestrial ecosystems. Nature 361:148–150

    Article  Google Scholar 

  • Davis GE, Kushner DJ, Mondragon JM, Mondragon JE, Lerma D, Richards D (1997) Kelp forest monitoring handbook, vol 1. Sampling protocol, Channel Islands National Park, Ventura, CA

  • Ebeling AW, Hixon MA (1991) Tropical and temperate reef fishes: comparison of community structure. In: Sale PF (ed) The ecology of fishes on coral reefs. Academic, San Diego, pp 509–563

    Google Scholar 

  • Edgar GJ, Banks S, Fariña JM, Calvopiña M, Martínez C (2004) Regional biogeography of shallow reef fish and macro-invertebrate communities in the Galapagos archipelago. J Biogeogr 31:1107–1124

    Article  Google Scholar 

  • Fänge R, Grove D (1979) Digestion. In: Hoar WS, Randall DJ, Brett JR (eds) Fish physiology. Bioenergetics and growth. Academic, New York, pp 162–260

    Google Scholar 

  • Ferreira CEL (1998) Resource partitioning by herbivores on a tropical rocky shore. PhD Thesis, Universidade Federal de São Carlos, São Paulo, Brazil (in Portuguese)

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

    Google Scholar 

  • Ferreira CEL, Floeter SR, Gasparini JL, Joyeux JC, Ferreira BP (2004) Trophic structure patterns of Brazilian reef fishes: a latitudinal comparison. J Biogeogr 31:1093–1106

    Article  Google Scholar 

  • Ferreira CEL, Gasparini JL, Carvalho-Filho A, Floeter SR (2005) A recently extinct parrotfish species from Brazil. Coral Reefs 24:128

    Article  Google Scholar 

  • Floeter SR, Guimarães RZP, Rocha LA, Ferreira CEL, Rangel CA, Gasparini JL (2001) Geographic variation in reef-fish assemblages along the Brazilian coast. Global Ecol Biogeogr 10:423–433

    Article  Google Scholar 

  • Floeter SR, Ferreira CEL, Dominici-Arosemena A, Zalmon I (2004) Latitudinal gradients in Atlantic reef fish communities: trophic structure and spatial use patterns. J Fish Biol 64:1680–1699

    Article  Google Scholar 

  • Francis M (1996) Geographic distribution of marine reef fishes in the New Zealand region. New Zeal J Mar Freshw Res 30:35–55

    Google Scholar 

  • Francour P (1997) Fish assemblages of Posidonia oceanica beds at Port-Cros (France, NW Mediterranean): assessment of composition and long term fluctuations by visual census. PSZN Mar Ecol 18:157–173

    Article  Google Scholar 

  • Gaines SD, Lubchenco J (1982) A unified approach to marine plant-herbivore interactions. II. Biogeography. Annu Rev Ecol Syst 13:111–138

    Article  Google Scholar 

  • Gatesoupe FJ, Lesel R (1998) An environmental approach to intestinal microflora in fish. Cah Agricult 7:29–35

    Google Scholar 

  • German DP, Horn MH, Gawlicka A (2004) Digestive enzyme activities in herbivorous and carnivorous prickleback fishes (Teleostei: Stichaeidae): ontogenetic, dietary, and phylogenetic effects. Physiol Biochem Zool 77:789–804

    Article  PubMed  CAS  Google Scholar 

  • Gillooly JF, Brown JH, West GB, Savage VM, Charnov EL (2001) Effects of size and temperature on metabolic rate. Science 293:2248–2251

    Article  PubMed  CAS  Google Scholar 

  • Hackney JM, Carpenter RC, Adey WH (1989) Characteristic adaptations to grazing among algal turfs on a Caribbean coral reef. Phycologia 28:109–119

    Google Scholar 

  • Harmelin-Vivien ML (2002) Energetics and fish diversity on coral reefs. In: Sale PF (ed) Coral reef fishes: dynamics and diversity in a complex ecosystem. Academic, San Diego, pp 265–274

    Google Scholar 

  • Hatcher BG (1981) The interaction between grazing organisms and the epilithic algal community of a coral reef: a quantitative assessment. In: Proceedings of the 4th international coral reef symposium, 2:515–524

  • Hatcher BG (1988) Coral reef primary productivity: a beggar’s banquet. Trends Ecol Evol 3:106–111

    Article  Google Scholar 

  • Hay ME (1991) Fish-seaweed interactions on corals reefs: effects of herbivorous fishes and adaptations of their prey. In: Sale PF (ed) The ecology of fishes on coral reefs. Academic, San Diego, pp 96–119

    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 

  • Horn MH (1989) Biology of marine herbivorous fishes. Oceanogr Mar Biol Annu Rev 27:167–272

    Google Scholar 

  • Horn MH, Gibson RN (1990) Effects of temperature on the food processing of three species of seaweed-eating fishes from European coastal waters. J Fish Biol 37:237–248

    Article  Google Scholar 

  • Horn MH, Ojeda FP (1999) Herbivory. In: Horn MH, Martin KLM, Chotkowski MA (eds) Intertidal fishes: life in two worlds. Academic, San Diego, pp 197–222

    Google Scholar 

  • Hughes TP (1996) Demographic approaches to community dynamics: a coral reef example. Ecology 77:2256–2260

    Article  Google Scholar 

  • Irelan CD, Horn MH (1991) Effects of macrophyte secondary chemicals on food choice and digestive efficiency of Cebidichthys violaceus (Girard), an herbivorous fish of temperate marine waters. J Exp Mar Biol Ecol 153:179–194

    Article  Google Scholar 

  • Jones GP (1988) Ecology of rocky reef fish on New Zealand: a review. Mar Freshw Res 22:445–462

    Google Scholar 

  • Jones GP, Andrew NL (1990) Herbivory and patch dynamics on rocky reefs in temperate Australasia, the role of fish and sea-urchins. Aust J Ecol 15:505–520

    Article  Google Scholar 

  • Kandel JS, Horn MH, Van Antwerp W (1994) Volatile fatty acids in the hindguts of herbivorous fishes from temperate and tropical marine waters. J Fish Biol 45:527–529

    Article  CAS  Google Scholar 

  • Leão ZMAN, Kikuchi RKP (2001) The Abrolhos reefs of Brazil. In: Seeliger U, Kjerfve B (eds) Ecological studies. Coastal Marine Ecosystems of Latin America, vol 144. Springer, Berlin, pp 83–96

  • Lewis SM (1986) The role of herbivorous fishes in the organization of a Caribbean reef community. Ecol Monogr 56:183–200

    Article  Google Scholar 

  • Lubchenco J, Gaines SD (1981) A unified approach to marine plant-herbivore interactions. I. Populations and communities. Annu Rev Ecol Syst 12:405–437

    Article  Google Scholar 

  • Maida M, Ferreira BP (1997) Coral reefs of Brazil: an overview. In: Proceedings of the 8th international coral reef symposium, 1:263–274

  • Mann KH (1973) Seaweeds: their productivity and strategy for growth. Science 182:975–981

    Article  PubMed  CAS  Google Scholar 

  • McKinon W, Alexander GJ (1999) Is temperature independence of digestive efficiency an experimental artifact in lizards? A test using the common flat lizard (Platysaurus intermedius). Copeia 199:299–303

    Article  Google Scholar 

  • Mead GW (1970) A history of South Pacific fishes. In: Wooster WS (ed) Scientific explorations of the South Pacific. National Academy of Sciences, Washington, pp 236–251

    Google Scholar 

  • Meekan MG, Choat JH (1997) Latitudinal variation in abundance of herbivorous fishes. Mar Biol 128:373–383

    Article  Google Scholar 

  • Miller MW (1998) Coral/seaweed competition and the control of reef community structure within and between latitudes. Oceanogr Mar Biol Annu Rev 36:65–96

    Google Scholar 

  • Mountfort DO, Campbell J, Clements KD (2002) Hindgut fermentation in three species of marine herbivorous fish. Appl Environ Microbiol 68:1374–1389

    Article  PubMed  CAS  Google Scholar 

  • Moura RL, Figueiredo JL, Sazima I (2001) A new parrotfish (Scaridae) from Brazil, and revalidation of Sparisoma frondosum (Agassiz, 1831), S. amplum (Ranzani, 1842), S. axillare (Steindachner, 1878) and Scarus trispinosus Valenciennes, 1840. Bull Mar Sci 68:505–524

    Google Scholar 

  • Myrick CA, Cech JJ Jr (2000) Temperature influences on California rainbow trout physiological performance. Fish Physiol Biochem 22:245–254

    Article  CAS  Google Scholar 

  • Olff H, Ritchie ME, Prins HHT (2002) Global environmental controls of diversity in large herbivores. Nature 415:901–904

    Article  PubMed  CAS  Google Scholar 

  • Polunin NVC, Klumpp DW (1992) A trophodynamic model of fish production on a windward coral-reef tract. In: John DM, Hawkins SJ, Price JH (eds) Plant-animal interactions in the marine benthos. Systematics Association Special Publication, vol 46. Clarendon, Oxford, pp 213–233

  • Pringle CM, Hamazaki T (1997) Effects of fishes on algal response to storms in a tropical stream. Ecology 78:2432–2442

    Google Scholar 

  • Pringle CM, Hamazaki T (1998) The role of omnivory in a neotropical stream: separating diurnal and nocturnal effects. Ecology 79:269–280

    Google Scholar 

  • Ralston SL, Horn MH (1986) High tide movements of the temperate-zone herbivorous fish Cebidichthys violaceus (Girard) as determined by ultrasonic telemetry. J Exp Mar Biol Ecol 98:35–50

    Article  Google Scholar 

  • Randall JE (1967) Food habits of reef fishes of the West Indies. Stud Trop Oceanogr 5:665–847

    Google Scholar 

  • Russell BC (1983) The food and feeding habits of rocky reef fish of northeastern New Zealand. New Zeal J Mar Freshw Res 17:121–145

    Article  Google Scholar 

  • Shurin JB, Borer ET, Seabloom EW, Anderson K, Blanchette CA, Broitman B, Cooper SD, Halpern BS (2002) A cross-ecosystem comparison of the strength of trophic cascades. Ecol Lett 5:785–791

    Article  Google Scholar 

  • Smith TB, Wahl DH, Mackie RI (1996) Volatile fatty acids and anaerobic fermentation in temperate piscivorous and omnivorous freshwater fish. J Fish Biol 48:829–841

    Article  CAS  Google Scholar 

  • Steinberg PD, Estes JA, Winter FC (1995) Evolutionary consequences of food chain length in kelp forest communities. Proc Natl Acad Sci USA 92:8145–8148

    Article  PubMed  CAS  Google Scholar 

  • Steneck RS (1983) Escalating herbivory and resulting adaptive trends in calcareous algal crusts. Paleobiology 9:44–61

    Google Scholar 

  • Steneck RS (1988) Herbivory on coral reefs: a synthesis. In: Proceedings of the 6th international coral reef symposium, 1:37–49

  • Stevens CE, Hume ID (1998) Contributions of microbes in the vertebrate gastrointestinal tract to production and conservation of nutrients. Physiol Rev 78:393–427

    PubMed  CAS  Google Scholar 

  • Stoddard KM (1985) A phylogenetic analysis of some prickleback fishes (Teleostei, Stichaeidae, Xiphisterinae) from the north Pacific Ocean, with a discussion of their biogeography. MA thesis, California State University, Fullerton

  • Sturm EA, Horn MH (1998) Food habits, gut morphology and pH, and assimilation efficiency of the zebraperch Hermosilla azurea, an herbivorous kyphosid fish of temperate marine waters. Mar Biol 132:515–522

    Article  Google Scholar 

  • Swihart RK, Bryant JP (2001) Importance of biogeography and ontogeny of woody plants in winter herbivory by mammals. J Mammal 82:1–21

    Article  Google Scholar 

  • Szmant AM (2001) Coral reef algal community dynamics. Coral Reefs 19:299–302

    Google Scholar 

  • Terborgh J (1973) On the notion of favorableness in plant ecology. Am Nat 107:481–501

    Article  Google Scholar 

  • Valentine JW, Roy K, Jablonski D (2002) Carnivore/non-carnivore ratios in northeastern Pacific marine gastropods. Mar Ecol Prog Ser 228:153–163

    Article  Google Scholar 

  • Van Alstyne KL, VJ Paul (1990) The biogeography of polyphenolic compounds in marine macroalgae: temperate brown algal defenses deter feeding by tropical herbivorous fishes. Oecologia 84:158–163

    Google Scholar 

  • Van Marken Lichtenbelt WD (1992) Digestion in an ectothermic herbivore, the green iguana (Iguana iguana): effect of food composition and body temperature. Physiol Zool 65:649–673

    Google Scholar 

  • Van Marken Lichtenbelt WD, Vogel JT, Wesselingh RA (1997) Energetic consequences of field body temperatures in the green iguana. Ecology 78:297–307

    Article  Google Scholar 

  • Vermeij GJ, Lindberg DR (2000) Delayed herbivory and the assembly of marine benthic ecosystems. Paleobiology 26:419–430

    Article  Google Scholar 

  • Westneat MW, Alfaro ME (2005) Phylogenetic relationships and evolutionary history of the reef fish family Labridae. Mol Phyl Evol (in press)

  • 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, 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 

  • Wooton TJ, Oemke MP (1992) Latitudinal differences in fish community trophic structure and the role of fish herbivory in a Costa Rica stream. Environ Biol Fish 35:311–319

    Article  Google Scholar 

  • Zar JH (1999) Biostatiscal analysis. 4th edn. Prentice Hall, Englewood Cliffs

    Google Scholar 

  • Zimmerman LC, CR Tracy (1989) Interactions between the environment and ectothermy and herbivory in reptiles. Physiol Zool 62:374–409

    Google Scholar 

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Acknowledgments

We thank K. Lafferty, A. Clark, M. Francis, J.H. Choat, P. Munday, S.C. Pennings, B. Hawkins, P. Buston, J.P. Barreiros, R.L. Moura, R. Stevens, D. Vázquez, F. Campón and A. Moles for exchanging ideas and/or providing unpublished records and literature. S.R.F. and C.E.L.F. thank the Smithsonian Tropical Research Institute for the STV grants for working in Panama; J.L. Gasparini, O.J. Luiz-Júnior, W. Krohling, M. Hostin, J.P. Barreiros, L.C. Gerhardinger, A.G.V. Floeter, IEAPM staff and D.R. Roberston (STRI) for invaluable help in the field and logistical support; Padi Aware Foundation, UENF and Fundação O Boticário de Proteção à Natureza (to S.R.F.), WWF (to C.E.L.F.) for financial support. Collection of data by M.J.P. was supported by the National Center for Caribbean Coral Reef Research through EPA grant# R828020 (Upper Florida Keys); NOAA-Fisheries Coral Reef Initiative (Key West), NSF grant OCE 0095955 to R.K. Cowen and C. Hughes (Caribbean), NOAA’s “Coral Reef Conservation Grant” (2003) to R.S. Steneck, National Undersea Research Center Caribbean Marine Research Center and the Pew Fellows Program for Marine Conservation Collaborative Grant (with T. McClanahan) (Bonaire); M.J.P. thanks M. Sullivan, K. Grorud-Colvert, A.L. Chapin, T. Boone, T.B. Smith, J. Llopiz, J. Purcell, M. Sullivan, R.K. Cowen, R.S. Steneck and S.M. Shellito for field support; M.W. Miller for field and logistical support as well as for facilitating the collaboration with S.R.F.; M.D.B. acknowledges the University of California Marine Council grant 01TCEQI081080 for essential funding. M.H.H. acknowledges NSF grant OCE-9906857 for financial support. This work was conducted while S.R.F. was Postdoctoral Associate at the National Center for Ecological Analysis and Synthesis, a center funded by NSF (Grant DEB-0072909) and the University of California, Santa Barbara.

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Floeter, S.R., Behrens, M.D., Ferreira, C.E.L. et al. Geographical gradients of marine herbivorous fishes: patterns and processes. Marine Biology 147, 1435–1447 (2005). https://doi.org/10.1007/s00227-005-0027-0

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