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Reef Fishes, Seaweeds, and Corals

A Complex Triangle

  • Chapter
Coral Reefs in the Anthropocene

Abstract

The coral-seaweed-herbivore triangle is an accepted generalization embedded within a highly complex web of biotic interactions and abiotic conditions that bring exceptions. The pattern is confirmed by observations that herbivorous fishes and urchins can have very strong effects on the standing crop of reef macroalgae, thereby opening space for corals to thrive. However, other factors, such as the abundance and distribution of territorial damselfishes, shelter for schooling herbivores, water motion, and nutrient flux, as well as multiple stressors on corals, can modify this basic pattern, sometimes strongly. High levels of herbivory lead to dominance by low-lying algae, including crustose corallines that may foster coral settlement. The intensity of herbivory by schooling fishes often varies unimodally with depth: low in very shallow water due to wave stress and other factors limiting accessibility by fishes, high at moderate depths, and low in deeper water where coral growth that provides shelter for fishes declines. Dense stands of macroalgae tend to thrive where herbivores are rare due to lack of habitat complexity that provides refuges from predation. Herbivorous damselfishes can act as natural cages by inhibiting schooling grazers and maintaining a high diversity of mid-successional algae within their territories via moderate grazing (intermediate-predation effect). These algal mats not only inhibit coral growth, but also serve as localized refugia for small invertebrates and newly settled fishes. Nutrients also play a pivotal role in structuring benthic algal productivity, standing crops, and species assemblages. Besides directly consuming corals or algae, reef fishes can also affect invertebrate corallivores and herbivores, causing subsequent indirect effects on reef benthos. Examples include predation on the corallivorous crown-of-thorns seastar and herbivorous sea urchins, the latter causing halos around patch reefs where urchins remain near cover. From a management perspective, conserving herbivores is clearly important for keeping reef algae in check. Maintaining both the abundance and species diversity of herbivores of a variety of sizes, especially via marine reserves, is likely the best means of ensuring that macroalgae do not displace corals. Such rules of thumb are likely essential for fostering the ecological resilience of coral reefs, especially in the context of a warming and acidifying ocean.

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References

  • Allen GR (1981) Butterflyfishes and angelfishes of the world. Mergus Publishers, Melle

    Google Scholar 

  • Allen GR (1991) Damselfishes of the world. Mergus Publishers, Melle

    Google Scholar 

  • Arnold SN, Steneck RS, Mumby PJ (2010) Running the gauntlet: inhibitory effects of algal turfs on the processes of coral recruitment. Mar Ecol Prog Ser 414:91–105

    Article  Google Scholar 

  • Aronson RB, Precht WF (2000) Herbivory and algal dynamics on the coral reef at Discovery Bay, Jamaica. Limnol Oceanogr 45:251–255

    Article  Google Scholar 

  • Bak RPM, Engel MS (1979) Distribution, abundance, and survival of juvenile hermatypic corals (Scleractinia) and the importance of life history stages in the parent coral community. Mar Biol 54:341–352

    Article  Google Scholar 

  • Barlow GW (1974) Extraspecihc imposition of social grazing among surgeonfishes (Pisces: Acanthuridae). J Zool 174:333–340

    Article  Google Scholar 

  • Barott KL, Williams GJ, Vermeij MJA, Harris J, Smith JE, Rohwer FL, Sandin SA (2012) Natural history of coral−algae competition across a gradient of human activity in the Line Islands. Mar Ecol Prog Ser 460:1–12

    Article  Google Scholar 

  • Bell JD, Harmelin-Vivien M, Galzin R (1985) Large scale spatial variation in the abundance of butterflyfishes (Chaetodontidae) on Polynesian reefs. Proc 5th Int Coral Reef Symp 5:421–426

    Google Scholar 

  • Belliveau SA, Paul VJ (2002) Effects of herbivory and nutrients on the early colonization of crustose coralline and fleshy algae. Mar Ecol Prog Ser 232:105–114

    Article  Google Scholar 

  • Bellwood DR, Choat JH (1990) A functional analysis of grazing in parrotfishes (family Scaridae): the ecological implications. Environ Biol Fish 28:189–214

    Article  Google Scholar 

  • Bellwood DR, Wainwright PC (2002) The history and biogeography of fishes on coral reefs. In: Sale PF (ed) Coral reef fishes: dynamics and diversity in a complex ecosystem. Academic, San Diego, pp 5–32

    Chapter  Google Scholar 

  • Bellwood DR, Hoey AS, Choat JH (2003) Limited functional redundancy in high diversity systems: resilience and ecosystem function on coral reefs. Ecol Lett 6:281–285

    Article  Google Scholar 

  • Bellwood DR, Hughes TP, Folke C, Nyström M (2004) Confronting the coral reef crisis. Nature 429:827–833

    Article  CAS  PubMed  Google Scholar 

  • Bellwood DR, Hughes TP, Hoey AS (2006) Sleeping functional group drives coral-reef recovery. Curr Biol 16:2434–2439

    Article  CAS  PubMed  Google Scholar 

  • Bellwood DR, Hoey AS, Hughes TP (2012) Human activity selectively impacts the ecosystem roles of parrotfishes on coral reefs. Proc R Soc B 279:1621–1629

    Article  PubMed Central  PubMed  Google Scholar 

  • Birkeland C (1977) The importance of rate of biomass accumulation in early successional stages of benthic communities to the survival of coral recruits. Proc 3rd Int Coral Reef Symp 1:15–21

    Google Scholar 

  • Birkeland C, Nelson SG, Wilkins S, Gates P (1985) Effects of grazing by herbivorous fishes on coral reef community metabolism. Proc 5th Int Coral Reef Symp 4:47–51

    Google Scholar 

  • Birrell CL, McCook LJ, Willis BL (2005) Effects of algal turfs and sediment on coral settlement. Mar Poll Bull 51:408–414

    Article  CAS  Google Scholar 

  • Birrell CL, McCook LJ, Willis BL, Harrington L (2008) Chemical effects of macroalgae on larval settlement of the broadcast spawning coral Acropora millepora. Mar Ecol Prog Ser 362:129–137

    Article  Google Scholar 

  • Bonaldo RM, Bellwood DR (2009) Dynamics of parrotfish grazing scars. Mar Biol 156:771–777

    Article  Google Scholar 

  • Bonaldo RM, Bellwood DR (2011) Parrotfish predation on massive Porites on the Great Barrier Reef. Coral Reefs 30:259–269

    Article  Google Scholar 

  • Bouchon-Navarro Y, Bouchon C (1989) Correlations between chaetodontid fishes and coral communities of the Gulf of Aqaba (Red Sea). Environ Biol Fish 25:1–3

    Article  Google Scholar 

  • Bouchon-Navarro Y, Bouchon C, Harmelin-Vivien ML (1985) Impact of coral degradation on a chaetodontid fish assemblage (Moorea, French Polynesia). Proc 5th Int Coral Reef Symp 5:427–432

    Google Scholar 

  • Box SJ, Mumby PJ (2007) Effect of macroalgal competition on growth and survival of juvenile Caribbean corals. Mar Ecol Prog Ser 342:139–149

    Article  Google Scholar 

  • Brawley SH, Adey WH (1977) Territorial behavior of threespot damselfish (Eupomacentrus planifrons) increases reef algal biomass and productivity. Environ Biol Fish 2:45–51

    Article  Google Scholar 

  • Brock RE (1979) An experimental study on the effects of grazing by parrotfishes and role of refuges in benthic community structure. Mar Biol 51:381–388

    Article  Google Scholar 

  • Bruckner AW, Bruckner RJ (1998) Destruction of coral by Sparisoma viride. Coral Reefs 17:350

    Article  Google Scholar 

  • Bruckner AW, Bruckner RJ, Sollins P (2000) Parrotfish predation on live coral: “spot biting” and “focused biting”. Coral Reefs 19:50

    Article  Google Scholar 

  • Bruno JF, Sweatman H, Precht WF, Selig ER, Schutte VGW (2009) Assessing evidence of phase shifts from coral to macroalgal dominance on coral reefs. Ecology 90:1478–1484

    Article  PubMed  Google Scholar 

  • Burkepile DE (2012) Context-dependent corallivory by parrotfishes in a Caribbean reef ecosystem. Coral Reefs 31:111–120

    Article  Google Scholar 

  • Burkepile DE, Hay ME (2006) Herbivore vs. nutrient control of marine primary producers: context-dependent effects. Ecology 87:3128–3139

    Article  PubMed  Google Scholar 

  • Burkepile DE, Hay ME (2008) Herbivore species richness and feeding complementarity affect community structure and function on a coral reef. Proc Natl Acad Sci U S A 105:16201–16206

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Burkepile DE, Hay ME (2010) Impact of herbivore identity on algal succession and coral growth on a Caribbean reef. PLoS ONE 5(1):e8963. doi:10.1371/journal.pone.0008963

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Burkepile DE, Allgeier JE, Shantz AA, Pritchard CE, Lemoine NP, Bhatti LH, Layman CA (2013) Nutrient supply from fishes facilitates macroalgae and suppresses corals in a Caribbean coral reef ecosystem. Sci Rep 3:e1493. doi:10.1038/srep01493

    Article  CAS  Google Scholar 

  • Carassou L, Leopold M, Guillemot N, Wantiez L, Kulbicki M (2013) Does herbivorous fish protection really improve coral reef resilience? A case study from New Caledonia (South Pacific). PLoS One 8(4), e60564

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Carpenter RC (1984) Predator and population density control of homing behavior in the Caribbean echinoid Diadema antillarum. Mar Biol 82:101–108

    Article  Google Scholar 

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

    Google Scholar 

  • Carpenter RC (1990) Mass mortality of Diadema antillarum II. Effects on population densities and grazing intensity of parrotfishes and surgeonfishes. Mar Biol 104:79–86

    Article  Google Scholar 

  • Ceccarelli DM, Jones GP, McCook LJ (2005) Foragers versus farmers: contrasting effects of two behavioural groups of herbivores on coral reefs. Oecologia 145:445–453

    Article  PubMed  Google Scholar 

  • Cheal AJ, MacNeil MA, Cripps E, Emslie MJ, Jonker M, Schaffelke B, Sweatman H (2010) Coral–macroalgal phase shifts or reef resilience: links with diversity and functional roles of herbivorous fishes on the Great Barrier Reef. Coral Reefs 29:1005–1015

    Article  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

    Chapter  Google Scholar 

  • Choat JH, Clements KD, Robbins WD (2002) The trophic status of herbivorous fishes on coral reefs: 1: 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. 2. Food processing modes and trophodynamics. Mar Biol 145:445–454

    Article  Google Scholar 

  • Chong-Seng KM, Cole AJ, Pratchett MS, Willis BL (2011) Selective feeding by coral reef fishes on coral lesions associated with brown band and black band disease. Coral Reefs 30:473–481

    Article  Google Scholar 

  • Clarke RD (1996) Population shifts in two competing fish species on a degrading coral reef. Mar Ecol Prog Ser 137:51–58

    Article  Google Scholar 

  • Cole AJ, Pratchett MS (2011a) Inter-specific variation in susceptibility to grazing among common reef corals. Mar Ecol Prog Ser 422:155–164

    Article  Google Scholar 

  • Cole AJ, Pratchett MS (2011b) Effects of juvenile coral-feeding butterflyfishes on host corals. Coral Reefs 30:623–630

    Article  Google Scholar 

  • Cole AJ, Pratchett MS, Jones GP (2008) Diversity and functional importance of coral-feeding fishes on tropical coral reefs. Fish Fisher 9:286–307

    Article  Google Scholar 

  • Cole AJ, Pratchett MS, Jones GP (2009) Effects of coral bleaching on the feeding response of two species of coral-feeding fish. J Exp Mar Biol Ecol 373:11–15

    Article  Google Scholar 

  • Cole AJ, Pratchett MS, Jones GP (2010) Corallivory in tubelip wrasses: diet, feeding and trophic importance. J Fish Biol 76:818–835

    Article  Google Scholar 

  • Cole AJ, Lawton RJ, Pratchett MS, Wilson SK (2011) Chronic coral consumption by butterflyfishes. Coral Reefs 30:85–93

    Article  Google Scholar 

  • Cole AJ, Lawton RJ, Wilson SK, Pratchett MS (2012) Consumption of tabular acroporid corals by reef fishes: a comparison with plant–herbivore interactions. Func Ecol 26:307–316

    Article  Google Scholar 

  • Cowman PF, Bellwood DR (2013) The historical biogeography of coral reef fishes: global patterns of origination and dispersal. J Biogeogr 40:209–224

    Article  Google Scholar 

  • Cox EF (1986) The effects of a selective corallivore on growth rates and competition for space between two species of Hawaiian corals. J Exp Mar Biol Ecol 101:161–174

    Article  Google Scholar 

  • Day RW (1977) Two contrasting effects of predation on species richness in coral reef habitats. Mar Biol 44:1–5

    Article  Google Scholar 

  • Diaz-Pulido G, McCook LJ (2003) Relative roles of herbivory and nutrients in the recruitment of coral-reef seaweeds. Ecology 84:2026–2033

    Article  Google Scholar 

  • Done TJ (1992) Phase shifts in coral reef communities and their ecological significance. Hydrobiologia 247:121–132

    Article  Google Scholar 

  • Duffy JE, Hay ME (1990) Seaweed adaptations to herbivory. BioSci 40:368–375

    Article  Google Scholar 

  • Eakin CM (1987) Damselfishes and their algal lawns: a case of plural mutualism. Symbiosis 4:275–288

    Google Scholar 

  • Edwards HJ, Elliott IA, Eakin CM, Irikawa A, Madin JS, McField M, Morgan JA, Van Woesik R, Mumby PJ (2010) How much time can herbivore protection buy for coral reefs under realistic regimes of hurricanes and coral bleaching? Glob Change Biol. doi:10.1111/j.1365-2486.2010.02366.x

    Google Scholar 

  • Ferreira CEL, Goncalves JEA, Coutinho R, Peret AC (1998) Herbivory by the dusky damselfish Stegastes fuscus (Cuvier, 1830) in a tropical rocky shore: effects on the benthic community. J Exp Mar Biol Ecol 229:241–264

    Article  Google Scholar 

  • Floeter SR, Behrens MD, Ferreira CEL, Paddack MJ, Horn MH (2005) Geographical gradients of marine herbivorous fishes: patterns and processes. Mar Biol 147:1435–1447

    Article  Google Scholar 

  • Foster SA (1985) Group foraging by a coral reef fish: a mechanism for gaining access to defended resources. Anim Behav 33:782–792

    Article  Google Scholar 

  • Foster SA (1987) The relative impacts of grazing by Caribbean coral reef fishes and Diadema: effects of habitat and surge. J Exp Mar Biol Ecol 105:1–20

    Article  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 

  • Glynn PW (1988) Predation on coral reefs: some key processes, concepts and research directions. Proc 6th Int Coral Reef Symp 1:51–62

    Google Scholar 

  • Glynn PW (1990) Feeding ecology of selected coral-reef macroconsumers: patterns and effects on coral community structure. In: Dubinsky Z (ed) Ecosystems of the world, vol. 25: coral reefs. Elsevier Science Publishing, New York, pp 365–400

    Google Scholar 

  • Glynn PW, Colgan MW (1988) Defense of corals and enhancement of coral diversity by territorial damselfishes. In: Proceedings of 6th international coral reef symposium 2:157–163

    Google Scholar 

  • Glynn PW, Wellington GM, Birkeland C (1979) Coral reef growth in the Galapagos: limitation by sea urchins. Science 203:47–49

    Google Scholar 

  • Graham NAJ, Evans RD, Russ GR (2003) The effects of marine reserve protection on the trophic relationships of reef fishes on the Great Barrier Reef. Environ Conserv 30:200–208

    Article  Google Scholar 

  • Graham NAJ, Bellwood DR, Cinner JE, Hughes TP, Norström AV, Nyström M (2013) Managing resilience to reverse phase shifts in coral reefs. Front Ecol Environ 11:541–548

    Article  Google Scholar 

  • Green AL (1992) Damselfish territories: focal sites for studies of the early life history of labroid fishes. Proc 7th Int Coral Reef Symp 1:601–605

    Google Scholar 

  • Green AL (1998) Spatio-temporal patterns of recruitment of labroid fishes (Pisces: Labridae and Scaridae) to damselfish territories. Environ Biol Fish 51:235–244

    Article  Google Scholar 

  • Gruner DS, Smith JE, Seabloom EW, Sandin SA, Ngai JT, Hillebrand H, Harpole WS, Elser JJ, Cleland EE, Bracken MES, Borer ET, Bolker BM (2008) A cross-system synthesis of consumer and nutrient resource control on producer biomass. Ecol Lett 11:740–755

    Article  PubMed  Google Scholar 

  • Harmelin-Vivien ML (1989) Reef fish community structure: an Indo-Pacific comparison. In: Harmelin-Vivien ML, Bourliere F (eds) Vertebrates in complex tropical systems. Springer, New York, pp 21–60

    Chapter  Google Scholar 

  • Harmelin-Vivien ML, Bouchon-Navarro Y (1981) Trophic relationships among chaetodontid fishes in the Gulf of Aqaba (Red Sea). Proc 4th Int Coral Reef Symp, Manila 2:537–544

    Google Scholar 

  • Harmelin-Vivien ML, Bouchon-Navarro Y (1983) Feeding diets and significance of coral feeding among chaetodontid fishes in Moorea (French Polynesia). Coral Reefs 2:119–127

    Google Scholar 

  • Harmelin-Vivien ML, Peyrot-Clausade M, Romano JC (1992) Transformation of algal turf by echinoids and scarid fishes on French Polynesian coral reefs. Coral Reefs 11:45–50

    Article  Google Scholar 

  • Hata H, Kato M (2002) Weeding by the herbivorous damselfish Stegastes nigricans in nearly monocultural algae farms. Mar Ecol Prog Ser 237:227–231

    Article  Google Scholar 

  • Hata H, Kato M (2003) Demise of monocultural algal farms by exclusion of territorial damselfish. Mar Ecol Prog Ser 263:159–167

    Article  Google Scholar 

  • Hata H, Nishihira M (2002) Territorial damselfish enhances multi-species co-existence of foraminifera mediated by biotic habitat structuring. J Exp Mar Biol Ecol 270:215–240

    Article  Google Scholar 

  • Hata H, Nishihira M, Kamura S (2002) Effects of habitat-conditioning by the damselfish Stegastes nigricans (Lacepède) on the community structure of benthic algae. J Exp Mar Biol Ecol 280:95–116

    Article  Google Scholar 

  • Hatcher BG (1981) The interaction between grazing organisms and the epilithic algal community of a coral reef: a quantitative assessment. Proc 4th Int Coral Reef Symp 2:515–524

    Google Scholar 

  • Hatcher BC (1990) Coral reef primary productivity: a hierarchy of pattern and process. Trends Ecol Evol 5:149–155

    Article  CAS  PubMed  Google Scholar 

  • Hatcher BG (1997) Organic production and decomposition. In: Birkeland C (ed) Life and death of coral reefs. Chapman & Hall, New York, pp 140–174

    Chapter  Google Scholar 

  • Hay ME (1981a) Spatial patterns of grazing intensity on a Caribbean barrier reef: herbivory and algal distribution. Aquat Bot 11:97–109

    Article  Google Scholar 

  • Hay ME (1981b) Herbivory, algal distribution, and the maintenance of between-habitat diversity on a tropical fringing reef. Am Nat 118:520–540

    Article  Google Scholar 

  • Hay ME (1984) Patterns of fish and urchin grazing on Caribbean coral reefs: are previous results typical? Ecology 65:446–454

    Article  Google Scholar 

  • Hay ME (1991) Fish-seaweed interactions on coral 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

    Chapter  Google Scholar 

  • Hay ME (1997) The ecology and evolution of seaweed-herbivore interactions on coral reefs. Coral Reefs 16(Suppl):S67–S76

    Article  Google Scholar 

  • Hay ME, Fenical W (1988) Marine plant-herbivore interactions: the ecology of chemical defense. Ann Rev Ecol Syst 19:111–145

    Article  Google Scholar 

  • Hay ME, Taylor PR (1985) Competition between herbivorous fishes and urchins on Caribbean reefs. Oecologia 65:591–598

    Article  Google Scholar 

  • Hay ME, Colburn T, Downing D (1983) Spatial and temporal patterns in herbivory on a Caribbean fringing reef: the effects on plant distribution. Oecologia 58:299–308

    Article  Google Scholar 

  • Heyward AJ, Negri AP (1999) Natural inducers for coral larval metamorphosis. Coral Reefs 18:273–279

    Article  Google Scholar 

  • Hinds PA, Ballantine DL (1987) Effects of the Caribbean threespot damselfish, Stegastes planifrons (Cuvier), on algal lawn composition. Aquat Bot 27:299–308

    Article  Google Scholar 

  • Hixon MA (1983) Fish grazing and community structure of reef corals and algae: a synthesis of recent studies. In: Reaka ML (ed) The ecology of coral reefs, NOAA Symposium Series Undersea Research, vol. 1. NOAA National Undersea Research Program,Rockville, pp 79–87

    Google Scholar 

  • Hixon MA (1986) Fish predation and local prey diversity. In: Simenstad CA, Cailliet GM (eds) Contemporary studies on fish feeding. Junk, Dordrecht, pp 235–257

    Chapter  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, San Diego, pp 475–508

    Chapter  Google Scholar 

  • Hixon MA (1997) The effects of reef fishes on corals and algae. In: Birkeland C (ed) Life and death of coral reefs. Chapman and Hall, New York, pp 230–248

    Google Scholar 

  • Hixon MA (2015) Predation: piscivory and the ecology of coral-reef fishes. In: Mora C (ed) Ecology and conservation of fishes on coral reefs: the functioning of an ecosystem in a changing world. Cambridge University Press, Cambridge, pp 41–54

    Google Scholar 

  • Hixon MA, Brostoff WN (1983) Damselfish as keystone species in reverse: intermediate disturbance and diversity of reef algae. Science 220:511–513

    Article  CAS  PubMed  Google Scholar 

  • Hixon MA, Brostoff WN (1985) Substrate characteristics, fish grazing, and epibenthic reef assemblages off Hawaii. Bull Mar Sci 37:200–213

    Google Scholar 

  • Hixon MA, Brostoff WN (1996) Succession and herbivory: effects of differential fish grazing on Hawaiian coral-reef algae. Ecol Mono 66:67–90

    Article  Google Scholar 

  • Hixon MA, Jones GP (2005) Competition, predation, and density-dependent mortality in demersal marine fishes. Ecology 86:2847–2859

    Article  Google Scholar 

  • Hixon MA, Menge BA (1991) Species diversity: prey refuges modify the interactive effects of predation and competition. Theor Popul Biol 39:178–200

    Article  Google Scholar 

  • 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 Mono 82:467–489

    Article  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 

  • Hoey AS, Bellwood DR (2011) Suppression of herbivory by macroalgal density: a critical feedback on coral reefs? Ecol Lett 14:267–273

    Article  PubMed  Google Scholar 

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

    Google Scholar 

  • Hourigan TF (1989) Environmental determinants of butterflyfish social systems. Environ Biol Fish 25:61–78

    Article  Google Scholar 

  • Hughes TP (1989) Community structure and diversity of coral reefs: the role of history. Ecology 70:275–279

    Article  Google Scholar 

  • Hughes TP (1994) Catastrophes, phase-shifts, and large-scale degradation of a Caribbean coral reef. Science 265:1547–1551

    Article  CAS  PubMed  Google Scholar 

  • Hughes TP, Baird AH, Dinsdale EA, Moltschaniwskyj NA, Pratchett MS, Tanner JE, Willis BL (1999) Patterns of recruitment and abundance of corals along the Great Barrier Reef. Nature 397:59–63

    Article  CAS  Google Scholar 

  • Hughes TP, Bellwood DR, Folke CS, McCook LJ, Pandolfi JM (2006) No-take areas, herbivory and coral reef resilience. Trends Ecol Evol 22:1–3

    Article  PubMed  Google Scholar 

  • Hughes TP, Rodrigues MJ, Bellwood DR, Ceccarelli D, Hoegh-Guldberg O, McCook L, Moltschaniwskyj N, Pratchett MS, Steneck RS, Willis B (2007) Phase shifts, herbivory, and the resilience of coral reefs to climate change. Curr Biol 17:360–365

    Article  CAS  PubMed  Google Scholar 

  • Hughes TP, Graham NAJ, Jackson JBC, Mumby PJ, Steneck RS (2010) Rising to the challenge of sustaining coral reef resilience. Trends Ecol Evol 25:633–642

    Article  PubMed  Google Scholar 

  • Hutchings PA (1986) Biological destruction of coral reefs: a review. Coral Reefs 4:239–252

    Article  Google Scholar 

  • Jackson JBC (1994) Constancy and change of life in the sea. Phil Trans R Soc B 344:55–60

    Article  Google Scholar 

  • Jackson JBC (1997) Reefs since Columbus. Coral Reefs 16(Suppl):S23–S32

    Article  Google Scholar 

  • Jayewardene D (2009) A factorial experiment quantifying the influence of parrotfish density and size on algal reduction on Hawaiian coral reefs. J Exp Mar Biol Ecol 375:64–69

    Article  Google Scholar 

  • Jayewardene D, Donahue MJ, Birkeland C (2009) Effects of frequent fish predation on corals in Hawaii. Coral Reefs 28:499–506

    Article  Google Scholar 

  • Jompa J, McCook LJ (1998) Seaweeds save the reefs?!: Sargassum canopy decreases coral bleaching on inshore reefs. Reef Res 8:5

    Google Scholar 

  • Jompa J, McCook LJ (2002) The effects of nutrients and herbivory on competition between a hard coral (Porites cylindrica) and a brown alga (Lobophora variegata). Limnol Oceanogr 47:527–534

    Article  CAS  Google Scholar 

  • Jones RS (1968) Ecological relationships in Hawaiian and Johnston Island Acanthuridae (surgeonfishes). Micronesica 4:309–361

    Google Scholar 

  • Jones GP, Befell 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, San Diego, pp 156–179

    Chapter  Google Scholar 

  • Kaufman LS (1977) The threespot damselfish: effects on benthic biota of Caribbean coral reefs. 3rd Int Coral Reef Symp 1:559–564

    Google Scholar 

  • Klumpp DW, Polunin NVC (1989) Partitioning among grazers of food resources within damselfish territories on a coral reef. J Exp Mar Biol Ecol 125:145–169

    Article  Google Scholar 

  • Klumpp DW, Pulfrich A (1989) Trophic significance of herbivorous macroinvertebrates on the central Great Barrier Reef. Coral Reefs 8:135–144

    Article  Google Scholar 

  • Klumpp DW, McKinnon D, Daniel P (1987) Damselfish territories: zones of high productivity on coral reefs. Mar Ecol Prog Ser 40:41–51

    Article  Google Scholar 

  • Knowlton N (1992) Thresholds and multiple stable states in coral reef community dynamics. Am Zool 32:674–679

    Article  Google Scholar 

  • Knowlton N, Lang JC, Keller BD (1990) Case study of natural population collapse: post-hurricane predation on Jamaican staghorn corals. Smithson Contr Mar Sci 31:1–25

    Article  Google Scholar 

  • Kokita T, Nakazono A (2001) Rapid response of an obligately corallivorous filefish Oxymonacanthus longirostris (Monacanthidae) to a mass coral bleaching event. Coral Reefs 20:155–158

    Article  Google Scholar 

  • Kuffner IB, Walters LJ, Becerro MA, Paul VJ, Ritson-Williams R, Beach KS (2006) Inhibition of coral recruitment by macroalgae and cyanobacteria. Mar Ecol Prog Ser 323:107–117

    Article  Google Scholar 

  • Lapointe BE (1997) Simultaneous top-down and bottom-up forces control macroalgal blooms on coral reefs. Limnol Oceanogr 44:1586–1592

    Google Scholar 

  • Lapointe BE (1999) Simultaneous top-down and bottom-up forces control macroalgal blooms on coral reefs (reply to the comment by Hughes et al.). Limnol Oceanogr 44:1586–1592

    CAS  Google Scholar 

  • Lapointe BE, Barile PJ, Yentsch CS, Littler MM, Littler DS, Kakuk B (2004) The relative importance of nutrient enrichment and herbivory on macroalgal communities near Norman’s Pond Cay, Exumas Cays, Bahamas: a “natural” enrichment experiment. J Exp Mar Biol Ecol 298:275–301

    Article  Google Scholar 

  • Larkum AWD (1983) The primary productivity of plant communities on coral reefs. In: Barnes DJ (ed) Perspectives on coral reefs. Australian Institute of Marine Science, Townsville, pp 221–230

    Google Scholar 

  • Lassuy DR (1980) Effects of “farming” behaviour by Eupomacentrus lividus and Hemiglyphidodon plagiometapon on algal community structure. Bull Mar Sci 30:304–312

    Google Scholar 

  • Ledlie MH, Graham NAJ, Bythell JC, Wilson SK, Jennings S, Polunin NVC, Hardcastle J (2007) Phase shifts and the role of herbivory in the resilience of coral reefs. Coral Reefs 26:641–653

    Article  Google Scholar 

  • Lessios HA (1988) Mass mortality of Diadema antillarum in the Caribbean: what have we learned? Ann Rev Ecol Syst 19:371–393

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Lewis SM, Wainwright PC (1985) Herbivore abundance and grazing intensity on a Caribbean coral reef. J Exp Mar Biol Ecol 87:215–228

    Article  Google Scholar 

  • Lirman D (2001) Competition between macroalgae and corals: effects of herbivore exclusion and increased algal biomass on coral survivorship and growth. Coral Reefs 19:392–399

    Article  Google Scholar 

  • Littler MM, Littler DS (1980) The evolution of thallus form and survival strategies in benthic marine macroalgae: field and laboratory tests of a functional form model. Am Nat 116:25–44

    Article  Google Scholar 

  • Littler MM, Littler DS (1984) Models of tropical reef biogenesis. Prog Phycol Res 3:323–364

    Google Scholar 

  • Littler MM, Taylor PR, Littler DS (1983) Algal resistance to herbivory on a Caribbean barrier reef. Coral Reefs 2:111–118

    Article  Google Scholar 

  • Littler MM, Taylor PR, Littler DS (1989) Complex interactions in the control of coral zonation on a Caribbean reef flat. Oecologia 80:331–340

    Article  Google Scholar 

  • Lobel PS (1980) Herbivory by damselfishes and their role in coral reef community ecology. Bull Mar Sci 30:273–289

    Google Scholar 

  • Low RM (1971) Interspecific territoriality in a pomacentrid reef fish, Pomacentrus flavicauda Whitley. Ecology 52:648–654

    Article  Google Scholar 

  • Mantyka CS, Bellwood DR (2007a) Direct evaluation of macroalgal removal by herbivorous coral reef fishes. Coral Reefs 26:435–442

    Article  Google Scholar 

  • Mantyka CS, Bellwood DR (2007b) Macroalgal grazing selectivity among herbivorous coral reef fishes. Mar Ecol Prog Ser 352:177–185

    Article  Google Scholar 

  • McCauley DJ, Micheli F, Young HS, Tittensor DP, Brumbaugh DR, Madin EMP, Holmes KE, Smith JE, Lotze HK, DeSalles PA, Arnold SN, Worm B (2010) Acute effects of removing large fish from a near-pristine coral reef. Mar Biol 157:2739–2750

    Article  PubMed Central  PubMed  Google Scholar 

  • McClanahan TR (1992) Resource utilization, competition, and predation: a model and example from coral reef grazers. Ecol Model 61:195–215

    Article  Google Scholar 

  • McClanahan TR (1997) Primary succession of coral-reef algae: differing patterns on fished versus unfished reefs. J Exp Mar Biol Ecol 218:77–102

    Article  Google Scholar 

  • McClanahan TR (2008) Response of the coral reef benthos and herbivory to fishery closure management and the 1998 ENSO disturbance. Oecologia 155:169–177

    Article  CAS  PubMed  Google Scholar 

  • McClanahan TR, Kamukuru AT, Muthiga NA, Yebio MG, Obura D (1996) Effect of sea urchin reductions on algae, coral, and fish populations. Cons Biol 10:136–154

    Article  Google Scholar 

  • McClanahan TR, Hendrick V, Rodrigues MJ, Polunin NVC (1999) Varying responses of herbivorous and invertebrate-feeding fishes to macroalgal reduction on a coral reef. Coral Reefs 18:195–203

    Article  Google Scholar 

  • McClanahan TR, Cokos BA, Sala E (2002) Algal growth and species composition under experimental control of herbivory, phosphorus and coral abundance in Glovers Reef, Belize. Mar Poll Bull 44:441–451

    Article  CAS  Google Scholar 

  • McClanahan TR, Huntington BE, Cokos B (2011a) Coral responses to macroalgal reduction and fisheries closure on Caribbean patch reefs. Mar Ecol Prog Ser 437:89–102

    Article  Google Scholar 

  • McClanahan TR, Muthiga NA, Coleman RA (2011b) Testing for top-down control: can post-disturbance fisheries closures reverse algal dominance? Aquatic Conserv Mar Freshw Ecosyst 21:658–675

    Article  Google Scholar 

  • McClanahan TR, Donner SD, Maynard JA, MacNeil MA, Graham NAJ, Maina J, Baker AC, I. JBA, Beger M, Campbell SJ, Darling ES, Eakin CM, Heron SF, Jupiter SD, Lundquist CJ, McLeod E, Mumby PJ, Paddack MJ, Selig ER, Van Woesik R (2012) Prioritizing key resilience indicators to support coral reef management in a changing climate. PLoS ONE 7(8), doi:10.1371/journal.pone.0042884

  • McCook LJ (1997) Effects of herbivory on zonation of Sargassum spp. within fringing reefs of the central Great Barrier Reef. Mar Biol 129:713–722

    Article  Google Scholar 

  • McCook LJ (1999) Macroalgae, nutrients and phase shifts on coral reefs: scientific issues and management consequences for the Great Barrier Reef. Coral Reefs 18:357–367

    Article  Google Scholar 

  • McCook LJ (2001) Competition between corals and algal turfs along a gradient of terrestrial influence in the nearshore central Great Barrier Reef. Coral Reefs 19:419–425

    Article  Google Scholar 

  • McCook LJ, Jompa J, Diaz-Pulido G (2001) Competition between corals and algae on coral reefs: a review of evidence and mechanisms. Coral Reefs 19:400–417

    Article  Google Scholar 

  • McManus JW, Polsenberg JF (2004) Coral–algal phase shifts on coral reefs: ecological and environmental aspects. Prog Ocean 60:263–279

    Article  Google Scholar 

  • McManus JW, Meñez LAB, Kesner-Reyes KN, Vergara SG, Ablan MC (2000) Coral reef fishing and coral-algal phase shifts: implications for global reef status. ICES J Mar Sci 57:572–578

    Article  Google Scholar 

  • Meyer JL, Schultz ET (1985a) Migrating haemulid fishes as a source of nutrients and organic matter on coral reefs. Limnol Oceanogr 30:146–156

    Article  Google Scholar 

  • Meyer JL, Schultz ET (1985b) Tissue condition and growth rate of corals associated with schooling fish. Limnol Oceanogr 39:157–166

    Article  Google Scholar 

  • Meyer JL, Schultz ET, Helfman GS (1983) Fish schools: an asset to corals. Science 220:1047–1049

    Article  CAS  PubMed  Google Scholar 

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

    Google Scholar 

  • Miller MW, Hay ME (1998) Effects of fish predation and seaweed competition on the survival and growth of corals. Oecologia 113:231–238

    Article  Google Scholar 

  • Miller MW, Hay ME, Miller SL, Malone D, Sotka EE, Szmant AM (1999) Effects of nutrients versus herbivores on reef algae: a new method for manipulating nutrients on coral reefs. Limnol Oceanogr 44:1847–1861

    Article  Google Scholar 

  • Montgomery WL (1980) The impact of non-selective grazing by the giant blue damselfish, Microspathodon dorsalis, on algal communities in the Gulf of California, Mexico. Bull Mar Sci 30:290–303

    Google Scholar 

  • Montgomery WL, Gerking SD (1980) Marine macroalgae as foods for fishes: an evaluation of potential food quality. Environ Biol Fish 5:143–153

    Article  Google Scholar 

  • Mora C (2015) Perpetual struggle for conservation in a crowded world and the needed paradigm shift for easing ultimate burdens. In: Mora C (ed) Ecology and conservation of fishes on coral reefs: the functioning of an ecosystem in a changing world. Cambridge University Press, Cambridge, pp 289–296

    Google Scholar 

  • Mora C, Andréfouët S, Costello MJ, Kranenburg C, Rollo A, Veron J, Gaston KJ, Myers RA (2006) Coral reefs and the global network of marine protected areas. Science 312:1750–1751

    Article  CAS  PubMed  Google Scholar 

  • Morrison D (1988) Comparing fish and urchin grazing in shallow and deeper coral reef algal communities. Ecology 69:1367–1382

    Article  Google Scholar 

  • Morse DE, Hooker N, Morse ANC, Jensen RA (1988) Control of larval metamorphosis and recruitment in sympatric agaricid corals. J Exp Mar Biol Ecol 116:193–212

    Article  Google Scholar 

  • Muir J (1911) My first summer in the Sierra. Houghton Mifflin, Boston

    Google Scholar 

  • Mumby PJ (2006) The impact of exploiting grazers (Scaridae) on the dynamics of Caribbean coral reefs. Ecol Appl 16:747–769

    Article  PubMed  Google Scholar 

  • Mumby PJ (2009) Phase shifts and the stability of macroalgal communities on Caribbean coral reefs. Coral Reefs 28:761–773

    Article  Google Scholar 

  • Mumby PJ, Dahlgren CP, Harborne AR, Kappel CV, Micheli F, Brumbaugh DR, Holmes KE, Mendes JM, Broad K, Sanchirico JN, Buch K, Box S, Stoffle RW, Gill AB (2006) Fishing, trophic cascades, and the process of grazing on coral reefs. Science 311:98-101

    Google Scholar 

  • Mumby PJ, Steneck RS (2008) Coral reef management and conservation in light of rapidly evolving ecological paradigms. Trends Ecol Evol 23:555–563

    Google Scholar 

  • Mumby PJ, Harborne AR, Williams J, Kappel CV, Brumbaugh DR, Micheli F, Holmes KE, Dahlgren CP, Paris CB, Blackwell PG (2007a) Trophic cascade facilitates coral recruitment in a marine reserve. Proc Natl Acad Sci U S A 104:8362–8367

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Mumby PJ, Hastings A, Edwards HJ (2007b) Thresholds and the resilience of Caribbean coral reefs. Nature 450:98–101

    Article  CAS  PubMed  Google Scholar 

  • Mumby PJ, Steneck RS, Edwards AJ, Ferrari R, Coleman R, Harborne AR, Gibson JP (2012) Fishing down a Caribbean food web relaxes trophic cascades. Mar Ecol Prog Ser 445:13–24

    Article  Google Scholar 

  • Mumby PJ, Steneck RS, Hastings A (2013) Evidence for and against the existence of alternate attractors on coral reefs. Oikos 122:481–491

    Article  Google Scholar 

  • Nelson SG, Tsutsui RN (1981) Browsing by herbivorous reef fishes on the agarophyte Gracilaria edulis (Rhodophyta) at Guam, Mariana Islands. Proc 4th Int Coral Reef Symp 2:503–506

    Google Scholar 

  • Neudecker S (1979) Effects of grazing and browsing fishes on the zonation of corals in Guam. Ecology 60:666–672

    Article  Google Scholar 

  • Nyström M, Folke C, Moberg F (2000) Coral reef disturbance and resilience in a human-dominated environment. Trends Ecol Evol 15:413–417

    Article  PubMed  Google Scholar 

  • Nyström M, Graham NAJ, Lokrantz J, Norström AV (2008) Capturing the cornerstones of coral reef resilience: linking theory to practice. Coral Reefs 27:795–809

    Article  Google Scholar 

  • Nyström M, Norström AV, Blenckner T, De la Torre-Castro M, Eklöf JS, Folke C, Österblom H, Steneck RS, Thyresson M, Troell M (2012) Confronting feedbacks of degraded marine ecosystems. Ecosystems 15:695–710

    Article  Google Scholar 

  • Ogden JC, Buckman NS (1973) Movements, foraging groups, and diurnal migrations of the striped parrotfish Scarus croicensis Bloch (Scaridae). Ecology 54:589–596

    Article  Google Scholar 

  • Ogden JC, Lobel PS (1978) The role of herbivorous fishes and urchins in coral reef communities. Environ Biol Fish 3:49–63

    Article  Google Scholar 

  • Ogden JC, Brown RA, Salesky N (1973) Grazing by the echinoid Diadema antillarum philippi: formation of halos around West Indian patch reefs. Science 182:715–717

    Article  CAS  PubMed  Google Scholar 

  • Ormond RFG, Head SH, Moore RJ, Rainbow PR, Saunders AP (1973) Formation and breakdown of aggregations of the crown-of-thorns starfish. Acanthaster planci (L.). Nature 246:167–169

    Article  Google Scholar 

  • Paddack MJ, Cowen RK, Sponaugle S (2006) Grazing pressure of herbivorous coral reef fishes on low coral-cover reefs. Coral Reefs 25:461–472

    Article  Google Scholar 

  • Paine RT (1966) Food web complexity and species diversity. Am Nat 100:65–75

    Article  Google Scholar 

  • Pandolfi JM, Jackson JBC, Baron N, Bradbury RH, Guzman HM, Hughes TP, Kappel CV, Micheli F, Ogden JC, Possingham HP, Sala E (2005) Are U.S. coral reefs on the slippery slope to slime? Science 307:1725–1726

    Article  CAS  PubMed  Google Scholar 

  • Patton WK (1974) Community structure among the animals inhabiting the coral Pocillopora damicornis at Heron Island. Australia. In: Frost SH, Weissand MP, Saunders JB (eds) Symbiosis in the sea. University of South Carolina Press, Columbia, pp 219–243

    Google Scholar 

  • Paulay G (1997) Diversity and distribution of reef organisms. In: Birkeland C (ed) Life and death of coral reefs. Chapman & Hall, New York, pp 298–353

    Chapter  Google Scholar 

  • Pearson RG, Endean R (1969) A preliminary study of the coral predator Acanthaster planci (L.) (Asteroidea) on the Great Barrier Reef. Notes Dept Harbours Marine, Qld, Aust 3:27–55

    Google Scholar 

  • Petraitis P (2013) Multiple stable states in natural ecosystems. Oxford University Press, Oxford

    Book  Google Scholar 

  • Polunin NVC (1988) Efficient uptake of algal production by a single resident herbivorous fish on a reef. J Exp Mar Biol Ecol 123:61–76

    Article  Google Scholar 

  • Polunin NVC, Koike I (1987) Temporal focusing of nitrogen release by a periodically feeding reef fish. J Exp Mar Biol Ecol 111:285–296

    Article  Google Scholar 

  • Polunin NVC, Roberts CM (eds) (1996) Reef fisheries. Chapman & Hall, London

    Google Scholar 

  • Potts DC (1977) Suppression of coral populations by filamentous algae within damselfish territories. J Exp Mar Biol Ecol 28:207–216

    Article  Google Scholar 

  • Pratchett MS, Gust N, Goby G, Klanten SO (2001) Consumption of coral propagules represents a significant trophic link between corals and reef fish. Coral Reefs 20:13–17

    Article  Google Scholar 

  • Randall JE (1961) Overgrazing of algae by herbivorous marine fishes. Ecology 42:812

    Article  Google Scholar 

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

    Google Scholar 

  • Randall JE (1974) The effects of fishes on coral reefs. Proc 2nd Int Coral Reef Symp 1:159–166

    Google Scholar 

  • Raymundo LJ, Halford AR, Maypa AP, Kerr AM (2009) Functionally diverse reef-fish communities ameliorate coral disease. Proc Natl Acad Sci U S A 106:17067–17070

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Reese ES (1975) A comparative field study of the social behavior and related ecology of reef fishes of the family Chaetodontidae. Z Tierpsychol 37:37–61

    Article  CAS  PubMed  Google Scholar 

  • Reese ES (1977) Coevolution of corals and coral feeding fishes of the family Chaetodontidae. Proc 3rd Int Coral Reef Symp 2:268–274

    Google Scholar 

  • Reese ES (1981) Predation on corals by fishes of the family Chaetodontidae: implications for conversation and management of coral reef ecosystems. Bull Mar Sci 31:594–604

    Google Scholar 

  • Reinthal PN, Lewis SM (1986) Social behavior, foraging efficiency and habitat utilization in a group of tropical herbivorous fish. Anim Behav 34:1687–1693

    Article  Google Scholar 

  • Roberts CM (1995) Effects of fishing on the ecosystem structure of coral reefs. Cons Biol 9:988–995

    Article  Google Scholar 

  • Roberts CM, Ormond RFG (1992) Butterflyfish social behaviour, with special reference to the incidence of territoriality: a review. Environ Biol Fish 34:79–93

    Article  Google Scholar 

  • Roberts CM, Ormond RFG, Shepherd ARD (1988) The usefulness of butterfly fishes as environmental indicators on coral reefs. Proc 6th Int Coral Reef Symp 2:331–336

    Google Scholar 

  • Robertson R (1970) Review of the predators and parasites of stony corals, with special reference to symbiotic prosobranch gastropods. Pac Sci 24:43–54

    Google Scholar 

  • 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, San Diego, pp 356–386

    Chapter  Google Scholar 

  • Robertson DR, Gaines SD (1986) Interference competition structures habitat use in a local assemblage of coral reef surgeonfishes. Ecology 67:1372–1383

    Article  Google Scholar 

  • Robertson DR, Sweatman HPA, Fletcher EA, Cleland MG (1976) Schooling as a mechanism for circumventing the territoriality of competitors. Ecology 57:1208–1220

    Article  Google Scholar 

  • Robertson DR, Polunin NVC, Leighton K (1979) The behavioral ecology of three Indian Ocean surgeonfishes (Acanthurus lineatus, A. leucosternum, and Zebrasoma scopas): their feeding strategies, and social and mating systems. Environ Biol Fish 4:125–170

    Article  Google Scholar 

  • Roff G, Mumby PJ (2012) Global disparity in the resilience of coral reefs. Trends Ecol Evol 27:404–413

    Article  PubMed  Google Scholar 

  • Rotjan RD, Dimond JL (2010) Discriminating causes from consequences of persistent parrotfish corallivory. J Exp Mar Biol Ecol 390:188–195

    Article  Google Scholar 

  • Rotjan RD, Lewis SM (2005) Selective predation by parrotfishes on the reef coral Porites astreoides. Mar Ecol Prog Ser 305:193–201

    Article  CAS  Google Scholar 

  • Rotjan RD, Lewis SM (2006) Parrotfish abundance and selective corallivory on a Belizean coral reef. J Exp Mar Biol Ecol 335:292–301

    Article  Google Scholar 

  • Rotjan RD, Lewis SM (2008) Impact of coral predators on tropical reefs. Mar Ecol Prog Ser 367:73–91

    Article  Google Scholar 

  • Rotjan RD, Lewis SM (2009) Predators selectively graze reproductive structures in a clonal marine organism. Mar Biol 156:569–577

    Article  Google Scholar 

  • Rotjan RD, Dimond JL, Thornhill DJ, Leichter JJ, Helmuth B, Kemp DW, Lewis SM (2006) Chronic parrotfish grazing impedes coral recovery after bleaching. Coral Reefs 25:361–368

    Article  Google Scholar 

  • Russ GR (1984a) 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 (1984b) Distribution and abundance of herbivorous grazing fishes in the central Great Barrier Reef. II. Patterns of zonation of mid-shelf and outershelf reefs. Mar Ecol Prog Ser 20:35–44

    Article  Google Scholar 

  • Russ GR (1987) Is the rate of removal of algae by grazers reduced inside territories of tropical damselfishes? J Exp Mar Biol Ecol 110:1–17

    Article  Google Scholar 

  • Russ GR (1991) Coral reef fisheries: effects and yields. In: Sale PF (ed) The ecology of fishes on coral reefs. Academic, San Diego, pp 601–635

    Chapter  Google Scholar 

  • Russ GR, St. John J (1988) Diets, growth rates and secondary production of herbivorous coral reef fishes. Proc 6th Int Coral Reef Symp 2:37–43

    Google Scholar 

  • Ruyter van Steveninck ED (1984) The composition of algal vegetation in and outside damselfish territories on a Florida reef. Aquat Bot 20:11–19

    Article  Google Scholar 

  • Sale PF (ed) (1991) The ecology of fishes on coral reefs. Academic, San Diego

    Google Scholar 

  • Sale PF (ed) (2002) Coral reef fishes: dynamics and diversity in a complex ecosystem. Academic, San Diego

    Google Scholar 

  • Sale PF, Hixon MA (2014) Addressing the global decline in coral reefs and forthcoming impacts on fishery yields. In: Bortone S (ed) Interrelationships between coral reefs and fisheries. CRC Press, Boca Raton, pp 7–18

    Google Scholar 

  • Sammarco PW (1983) Effects of fish grazing and damselfish territoriality on coral reef algae. I. Algal community structure. Mar Ecol Prog Ser 13:1–14

    Article  Google Scholar 

  • Sammarco PW, Carleton JH (1981) Damselfish territoriality and coral community structure: reduced grazing, coral recruitment, and effects on coral spat. Proc 4th Int Coral Reef Symp 2:525–535

    Google Scholar 

  • Sammarco PW, Williams AH (1982) Damselfish territoriality: influences on Diadema distribution and implications for coral community structure. Mar Ecol Prog Ser 8:53–59

    Article  Google Scholar 

  • Sandin SA, Smith JE, DeMartini EE, Dinsdale EA, Donner SD, Friedlander AM, Konotchick T, Malay M, Maragos JE, Obura D, Pantos O, Paulay G, Richie M, Rohwer F, Schroeder RE, Walsh S, Jackson JBC, Knowlton N, Sala E (2008) Baselines and degradation of coral reefs in the northern Line Islands. PLoS One 3(2), e1548. doi:10.1371/journal.pone.0001548

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Sano M, Shimizu M, Nose Y (1987) Long-term effects of destruction of hermatypic corals by Acanthaster planci infestation on reef fish communities at Iriomote Island, Japan. Mar Ecol Prog Ser 37:191–199

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Sebastián CR, McClanahan TR (2013) Description and validation of production processes in the coral reef ecosystem model CAFFEE (Coral–Algae–Fish-Fisheries Ecosystem Energetics) with a fisheries closure and climatic disturbance. Ecol Model 263:326–348

    Article  Google Scholar 

  • Selig ER, Bruno JF (2010) A global analysis of the effectiveness of marine protected areas in preventing coral loss. PLoS One 5(2):e9278. doi:10.1371/journal.pone.0009278

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  • Sluka RD, Miller MW (2001) Herbivorous fish assemblages and herbivory pressure on Laamu Atoll, Republic of Maldives. Coral Reefs 20:255–262

    Article  Google Scholar 

  • Smith CL, Tyler JC (1972) Space resource sharing in a coral reef fish community. Bull Nat Hist Mus Los Angeles Co 14:125–170

    Google Scholar 

  • Smith JE, Smith CM, Hunter CL (2001) An experimental analysis of the effects of herbivory and nutrient enrichment on benthic community dynamics on a Hawaiian reef. Coral Reefs 19:332–342

    Article  Google Scholar 

  • Smith JE, Shaw M, Edwards RA, Obura D, Pantos O, Sala E, Sandin SA, Smriga S, Hatay M, Rohwer FL (2006) Indirect effects of algae on coral: algae-mediated, microbe-induced coral mortality. Ecol Lett 9:835–845

    Article  PubMed  Google Scholar 

  • Smith JE, Hunter CL, Smith CM (2010) The effects of top–down versus bottom–up control on benthic coral reef community structure. Oecologia 163:497–507

    Article  PubMed  Google Scholar 

  • Sotka EE, Hay ME (2009) Effects of herbivores, nutrient enrichment, and their interactions on macroalgal proliferation and coral growth. Coral Reefs 28:555–568

    Article  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. Proc 6th Int Coral Reef Symp 1:37–49

    Google Scholar 

  • Steneck RS, Paris CB, Arnold SN, Ablan-Lagman MC, Alcala AC, Butler MJ, McCook LJ, Russ GR, Sale PF (2009) Thinking and managing outside the box: coalescing connectivity networks to build region-wide resilience in coral reef ecosystems. Coral Reefs 28:367–378

    Article  Google Scholar 

  • Stephenson W, Searles RB (1960) Experimental studies on the ecology of intertidal environments of Heron Island. I. Exclusion of fish from beach rock. Aust J Mar Freshw Res 2:241–267

    Article  Google Scholar 

  • Stimson J, Larned ST, Conklin E (2001) Effects of herbivory, nutrient levels, and introduced algae on the distribution and abundance of the invasive macroalga Dictyosphaeria cavernosa in Kaneohe Bay, Hawaii. Coral Reefs 19:343–357

    Article  Google Scholar 

  • Suefuji M, van Woesik R (2001) Coral recovery from the 1998 bleaching event is facilitated in Stegastes (Pisces: Pomacentridae) territories, Okinawa, Japan. Coral Reefs 20:385–386

    Article  Google Scholar 

  • Sweatman HPA (1995) A field study of fish predation on juvenile crown-of-thorns starfish. Coral Reefs 14:47–53

    Article  Google Scholar 

  • Szmant AM (2001) Why are coral reefs world-wide becoming overgrown by algae? Algae, algae everywhere, and nowhere a bite to eat! Coral Reefs 19:299–302

    Article  Google Scholar 

  • Tanner JE (1995) Competition between scleractinian corals and macroalgae: an experimental investigation of coral growth, survival, and reproduction. J Exp Mar Biol Ecol 190:151–168

    Article  Google Scholar 

  • Thacker RW, Ginsburg DW, Paul VJ (2001) Effects of herbivore exclusion and nutrient enrichment on coral reef macroalgae and cyanobacteria. Coral Reefs 19:318–329

    Article  Google Scholar 

  • Tricas TM (1989) Determinants of feeding territory size in the corallivorous butterfly fish, Chaetodon multicinctus. Anim Behav 37:830–841

    Article  Google Scholar 

  • Van den Hoek C, Cortel-Breeman AM, Wanders JBW (1975) Algal zonation in the fringing coral reef of Caracas, Netherlands Antillies, in relation to zonation of corals and gorgonians. Aquat Bot 1:269–308

    Article  Google Scholar 

  • Van den Hoek C, Breeman AM, Bak RPM, van Buurt G (1978) The distribution of algae, corals, and gorgonians in relation to depth, light attenuation, water movement and grazing pressure in the fringing coral reef of Curacao, Netherlands Antilles. Aquat Bot 5:1–46

    Article  Google Scholar 

  • Vermeij MJA, van der Heijden RA, Olthuis JG, Marhaver KL, Smith JE, Visser PM (2013) Survival and dispersal of turf algae and macroalgae consumed by herbivorous coral reef fishes. Oecologia 171:417–425

    Article  PubMed  Google Scholar 

  • Vine PJ (1974) Effects of algal grazing and aggressive behaviour of the fishes Pomacentrus lividus and Acanthurus sohal on coral-reef ecology. Mar Biol 24:131–136

    Article  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 ecosystem. Academic, San Diego, pp 33–55

    Chapter  Google Scholar 

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

    Article  Google Scholar 

  • Weber JN, Woodhead PMJ (1970) Ecological studies of the coral predator Acanthaster planci in the South Pacific. Mar Biol 6:12–17

    Article  Google Scholar 

  • Wellington GM (1982) Depth zonation of corals in the Gulf of Panama: control and facilitation by resident reef fish. Ecol Mono 52:223–241

    Article  Google Scholar 

  • Westneat MW, Resing JM (1988) Predation on coral spawn by planktivorous fish. Coral Reefs 7:89–92

    Article  Google Scholar 

  • White AT (1988) Chaetodon occurrence relative to coral reef habitats in the Philippines with implications for reef assessment. Proc 6th Int Coral Reef Symp 2:427–431

    Google Scholar 

  • Wilkinson CR, Sammarco PW (1983) Effects of fish grazing and damselfish territoriality on coral reef algae. II. Nitrogen fixation. Mar Ecol Prog Ser 13:15–19

    Google Scholar 

  • Williams AH (1980) The threespot damselfish: a noncarnivorous keystone species. Am Nat 116:138–142

    Google Scholar 

  • Williams AH (1981) An analysis of competitive interactions in a patchy back-reef environment. Ecology 62:1107–1120

    Article  Google Scholar 

  • Williams DM (1986) Temporal variation in the structure of reef slope fish communities (central Great Barrier Reef): short-term effects of Acanthaster planci infestation. Mar Ecol Prog Ser 28:157–164

    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 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

    Article  Google Scholar 

  • Williams ID, Polunin NVC, Hendrick VJ (2001) Limits to grazing by herbivorous fishes and the impact of low coral cover on macroalgal abundance on a coral reef in Belize. Mar Ecol Prog Ser 222:187–196

    Article  Google Scholar 

  • Winterbottom R, Emery AR (1981) A new genus and two new species of gobiid fishes (Perciformes) from the Chagos Archipelago, Central Indian Ocean. Environ Biol Fish 6:139–149

    Article  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 

  • Zeller DC (1988) Short-term effects of territoriality of a tropical damsel fish 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

I thank Chuck Birkeland for his perseverance and patience in completing this volume. I offer my sincere apologies to authors of any highly relevant publications I missed in my literature search. I thank the U.S. National Science Foundation for funding my research cited herein. This chapter is dedicated to my new grandson, Nolan Barrett Broeder, to the memory of Gerry Wellington, and to all those who actively work to save our remaining coral reefs, so that Nolan and his generation may experience these rainbow wonders of nature.

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Correspondence to Mark A. Hixon .

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Hixon, M.A. (2015). Reef Fishes, Seaweeds, and Corals. In: Birkeland, C. (eds) Coral Reefs in the Anthropocene. Springer, Dordrecht. https://doi.org/10.1007/978-94-017-7249-5_10

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