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Larval settlement preferences of Acropora palmata and Montastraea faveolata in response to diverse red algae

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Abstract

Settlement specificity can regulate recruitment but remains poorly understood for coral larvae. We studied larvae of the corals, Acropora palmata and Montastraea faveolata, to determine their rates of settlement and metamorphosis in the presence of ten species of red algae, including eight species of crustose coralline algae, one geniculated coralline and one encrusting peyssonnelid. Twenty to forty percent of larvae of A. palmata settled on coralline surfaces of Hydrolithon boergesenii, Lithoporella atlantica, Neogoniolithon affine, and Titanoderma prototypum, whereas none settled and metamorphosed on Neogoniolithon mamillare. Larvae of M. faveolata had 13–25 % settlement onto the surface of Amphiroa tribulus, H. boergesenii, N. affine, N. munitum, and T. prototypum, but had no settlement on the surface of N. mamillare, Porolithon pachydermum, and a noncoralline crust Peyssonnelia sp. Some of these algal species were common on Belizean reefs, but the species that induced the highest rates of larval settlement and metamorphosis tended to be rare and primarily found in low-light environments. The shallow coral, A. palmata, and the deeper coral, M. faveolata, both had increased larval settlement rates in the presence of only a few species of red algae found at deeper depths suggesting that patterns of coral distribution can only sometimes be related to the distribution of red algae species.

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References

  • Adey WH (1970) A revision of the Foslie crustose coralline herbarium. Det K Nor Vidensk Selsk Skr 1:1–46

    Google Scholar 

  • Adey WH, Adey PJ (1973) Studies on the biosystematics and ecology of the epilithic crustose Corallinaceae of the British Isles. Br Phycol J 8:343–407

    Article  Google Scholar 

  • Adey WH, Steneck RS (2001) Thermogeography over time creates biogeographic regions: a temperature/space/time-integrated model and an abundance-weighted test for benthic marine algae. J Phycol 37:677–698

    Article  Google Scholar 

  • Adey WH, Townsend RA, Boykins WT (1982) The crustose coralline algae (Rhodophyta:Corallinaceae) of the Hawaiian islands. Smithson Contrib Mar Sci 15:1–74

    Article  Google Scholar 

  • Arnold SN, Steneck RS (2011) Settling into an increasingly hostile world: the rapidly closing “recruitment window” for corals. PLoS ONE 6:e28681

    Article  CAS  PubMed Central  PubMed  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 

  • Baird AH, Hughes TP (1997) Spatial variation in coral recruitment around Lizard Island, Australia. Proc 8th Int Coral Reef Symp 2:1207–1210

    Google Scholar 

  • Baird AH, Babcock RC, Mundy CP (2003) Habitat selection by larvae influences the depth distribution of six common coral species. Mar Ecol Prog Ser 252:289–293

    Article  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

  • Birrell CL, McCook LJ, Willis BL, Diaz-Pulido G (2008) Effects of benthic algae on the replenishment of corals and the implications for the resilience of coral reefs. Oceanogr Mar Biol Annu Rev 46:25–63

    Google Scholar 

  • Bittner L, Payri CE, Maneveldt GW, Couloux A, Cruaud C, de Reviers B, Le Gall L (2011) Evolutionary history of the Corallinales (Corallinophycidae, Rhodophyta) inferred from nuclear, plastidial and mitochondrial genomes. Mol Phylogenet Evol 61:697–713

    Article  CAS  PubMed  Google Scholar 

  • Brandt ME, McManus JW (2009) Disease incidence is related to bleaching extent in reef-building corals. Ecology 90:2859–2867

    Article  PubMed  Google Scholar 

  • Bruno JF, Selig ER (2007) Regional decline of coral cover in the Indo-Pacific: timing, extent, and subregional comparisons. PLoS ONE 2(8):e711

    Article  PubMed Central  PubMed  Google Scholar 

  • Carlon DB (2002) Production and supply of larvae as determinants of zonation in a brooding tropical coral. J Exp Mar Biol Ecol 268:33–46

    Article  Google Scholar 

  • Doropoulis C, Ward S, Diaz-Pulido G, Hoegh-Guldberg O, Mumby PJ (2012) Ocean acidification reduces coral recruitment by disrupting intimate larval-algal settlement interactions. Ecol Lett 15:338–346

    Article  Google Scholar 

  • Gaines S, Roughgarden J (1985) Larval settlement rate - a leading determinant of structure in an ecological community of the marine intertidal zone. Proc Natl Acad Sci USA 82:3707–3711

    Article  CAS  PubMed  Google Scholar 

  • Gleason DF, Danilowicz BS, Nolan CJ (2009) Reef waters stimulate substratum exploration in planulae from brooding Caribbean corals. Coral Reefs 28:549–554

    Article  Google Scholar 

  • Golbuu Y, Richmond RH (2007) Substratum preferences in planula larvae of two species of scleractinian corals, Goniastrea retiformis and Stylaraea punctata. Mar Biol 152:639–644

    Article  Google Scholar 

  • Gordon GD, Masaki T, Akioka H (1976) Floristic and distributional account of the common crustose coralline algae on Guam. Micronesica 12:247–277

    Google Scholar 

  • Hadfield MG (2011) Biofilms and marine invertebrate larvae: what bacteria produce that larvae use to choose settlement sites. Annu Rev Mar Sci 3:453–470

    Article  Google Scholar 

  • Hadfield MG, Paul VJ (2001) Natural chemical cues for settlement and metamorphosis of marine-invertebrate larvae. In: McClintock J, Baker B (eds) Marine chemical ecology. CRC Press, Boca Raton, pp 431–462

    Chapter  Google Scholar 

  • Halpern BS, Walbridge S, Selkoe KA, Kappel CV, Micheli F, D’Agrosa C, Bruno JF, Casey KS, Ebert C, Fox HE, Fujita R, Heinemann D, Lenihan HS, Madin EMP, Perry MT, Selig ER, Spalding M, Steneck R, Watson R (2008) A global map of human impact on marine ecosystems. Science 319:948–952

    Article  CAS  PubMed  Google Scholar 

  • Harrington L, Fabricius K, De’ath G, Negri A (2004) Recognition and selection of settlement substrata determine post-settlement survival in corals. Ecology 85:3428–3437

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Kato A, Baba M, Suda S (2011) Revision of Mastophoroideae (Corallinales, Rhodophyta) and polyphyly in nongeniculate species widely distributed on Pacific coral reefs. J Phycol 47:662–672

    Article  Google Scholar 

  • Kuffner IB, Paul VJ (2004) Effects of the benthic cyanobacterium Lyngbya majuscula on the larval settlement of the reef corals Acropora surculosa and Pocillopora damicornis. Coral Reefs 23:455–458

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Littler DS, Littler MM (2000) Caribbean reef plants: An identification guide to the reef plants of the Caribbean, Bahamas, Florida and Gulf of Mexico. OffShore Graphics Inc, Washington, DC

    Google Scholar 

  • Mason B, Beard M, Miller MW (2011) Coral larvae settle at a higher frequency on red surfaces. Coral Reefs 30:667–676

    Article  Google Scholar 

  • Miller J, Muller E, Rogers C, Waara R, Atkinson A, Whelan KRT, Patterson M, Witcher B (2009a) Coral disease following massive bleaching in 2005 causes 60% decline in coral cover on reefs in the US Virgin Islands. Coral Reefs 28:925–937

    Article  Google Scholar 

  • Miller MW, Valdivia A, Kramer KL, Mason B, Williams DE, Johnston L (2009b) Alternate benthic assemblages on reef restoration structures and cascading effects on coral settlement. Mar Ecol Prog Ser 387:147–156

    Article  Google Scholar 

  • Morse DE, Morse ANC (1991) Enzymatic characterization of the morphogen recognized by Agaricia humilis (scleractinian coral) larvae. Biol Bull 181:104–122

    Article  Google Scholar 

  • Morse DE, Hooker N, Morse ANC, Jensen RA (1988) Control of larval metamorphosis and recruitment in sympatric agariciid corals. J Exp Mar Biol Ecol 116:193–217

    Article  Google Scholar 

  • Morse DE, Morse ANC, Raimondi PT, Hooker N (1994) Morphogen-based chemical flypaper for Agaricia humilis coral larvae. Biol Bull 186:172–181

    Article  CAS  Google Scholar 

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

    Article  PubMed  Google Scholar 

  • Mundy CN, Babcock RC (1998) Role of light intensity and spectral quality in coral settlement: implications for depth-dependent settlement? J Exp Mar Biol Ecol 223:235–255

    Article  Google Scholar 

  • Mundy CN, Babcock RC (2000) Are vertical distribution patterns of scleractinian corals maintained by pre- or post-settlement processes? A case study of three contrasting species. Mar Ecol Prog Ser 198:109–119

    Article  Google Scholar 

  • Negri AP, Webster NS, Hill RT, Heyward AJ (2001) Metamorphosis of broadcast spawning corals in response to bacteria isolated from crustose algae. Mar Ecol Prog Ser 223:121–131

    Article  Google Scholar 

  • NMFS (2006) Endangered and threatened species: final listing determinations for Elkhorn coral and Staghorn coral. Federal Register 71:26852–26861

    Google Scholar 

  • O’Leary JK, McClanahan TR (2010) Trophic cascades results in large-scale coralline algae loss through differential grazer effects. Ecology 91:3584–3597

    Article  PubMed  Google Scholar 

  • O’Leary JK, Potts DC, Braga JC, McClanahan TR (2012) Indirect consequences of fishing: reduction of coralline algae suppresses juvenile coral abundance. Coral Reefs 31:547–559

    Article  Google Scholar 

  • Pandolfi JM, Jackson JB (2006) Ecological persistence interrupted in Caribbean coral reefs. Ecol Lett 9:818–826

    Article  PubMed  Google Scholar 

  • Paul VJ, Kuffner IB, Walters LJ, Ritson-Williams R, Beach K, Becerro MA (2011) Chemically mediated interactions between macroalgae Dictyota spp. and multiple life-history stages of the coral Porites astreoides. Mar Ecol Prog Ser 426:161–170

    Article  Google Scholar 

  • Pawlik JR (1992) Chemical ecology of the settlement of benthic marine invertebrates. Oceanogr Mar Biol Annu Rev 30:273–335

    Google Scholar 

  • Penin L, Michonneau F, Baird AH, Connolly SR, Pratchett MS, Kayal M, Adjeroud M (2010) Early post-settlement mortality and the structure of coral assemblages. Mar Ecol Prog Ser 408:55–64

    Article  Google Scholar 

  • Price N (2010) Habitat selection, facilitation, and biotic settlement cues affect distribution and performance of coral recruits in French Polynesia. Oecologia 163:747–758

    Article  PubMed Central  PubMed  Google Scholar 

  • Raimondi PT, Morse ANC (2000) The consequences of complex larval behavior in a coral. Ecology 81:3193–3211

    Article  Google Scholar 

  • Ritson-Williams R, Paul VJ, Arnold S, Steneck RS (2010) Larval settlement preferences and post-settlement survival of the threatened Caribbean corals Acropora palmata and A. cervicornis. Coral Reefs 29:71–81

    Article  Google Scholar 

  • Ritson-Williams R, Arnold S, Fogarty N, Steneck RS, Vermeij M, Paul VJ (2009) New perspectives on ecological mechanisms affecting coral recruitment on reefs. Smithson Contrib Mar Sci 38:437–457

    Article  Google Scholar 

  • Rogers CS, Fitz HC III, Gilnack M, Beets J, Hardin J (1984) Scleractinian coral recruitment patterns at Salt River Submarine Canyon, St. Croix, U.S. Virgin Islands. Coral Reefs 3:69–76

    Article  Google Scholar 

  • Stake JL, Sammarco PW (2003) Effects of pressure on swimming behavior in planula larvae of the coral Porites astreoides (Cnidaria, Scleractinia). J Exp Mar Biol Ecol 288:181–201

    Article  Google Scholar 

  • Steneck RS (1986) The ecology of coralline algal crusts: convergent patterns and adaptive strategies. Annu Rev Ecol Syst 17:273–303

    Article  Google Scholar 

  • Steneck RS (1997) Crustose corallines, other algal functional groups, herbivores and sediments: complex interactions along reef productivity gradients. Proc 8th Int Coral Reef Symp 1:695–700

    Google Scholar 

  • Taylor WR (1960) Marine algae of the eastern tropical and subtropical coasts of the Americas. University of Michigan studies Vol. 21, University of Michigan Press, Ann Arbor, p 870

  • Tran C, Hadfield MG (2011) Larvae of Pocillopora damicornis (Anthozoa) settle and metamorphose in response to surface-biofilm bacteria. Mar Ecol Prog Ser 433:85–96

    Article  Google Scholar 

  • Underwood AJ, Fairweather PG (1989) Supply-side ecology and benthic marine assemblages. Trends Ecol Evol 4:16–20

    Article  CAS  PubMed  Google Scholar 

  • Vermeij MJA, Fogarty ND, Miller MW (2006) Pelagic conditions affect larval behavior, survival, and settlement patterns in the Caribbean coral Montastraea faveolata. Mar Ecol Prog Ser 310:119–128

    Article  Google Scholar 

  • Vermeij MJA, Marhaver KL, Huijbers CM, Nagelkerken I, Simpson SD (2010) Coral larvae move toward reef sounds. PLoS ONE 5:e10660

    Article  PubMed Central  PubMed  Google Scholar 

  • Wallace CC (1985) Seasonal peaks and annual fluctuations in recruitment of juvenile scleractinian corals. Mar Ecol Prog Ser 21:289–298

    Article  Google Scholar 

  • Webster NS, Smith LD, Heyward AJ, Watts JEM, Web RI, Blackall LL, Negri AP (2004) Metamorphosis of a scleractinian coral in response to microbial biofilms. Appl Environ Microbiol 70:1213–1221

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Woelkerling WJ (1988) The coralline red algae: An analysis of the genera and subfamilies of nongeniculate Corallinaceae. British Museum and Oxford University Press, London

    Google Scholar 

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Acknowledgments

Special thanks to Nikki Fogarty for advice, intellectual discussions, and help with our experiments. We appreciate the logistical support of Klaus Ruetzler, Michael Carpenter, Zach Foltz, and Scott Jones for facilitating our work at Carrie Bow Cay. Belize Fisheries Department provided us with permits to conduct this research. This work was supported by the Hunterdon Oceanographic Fund and the Marine Science Network at the Smithsonian Institution. This is contribution number 953 of the Caribbean Coral Reef Ecosystems program and 935 of the Smithsonian Marine Station at Fort Pierce.

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Correspondence to R. Ritson-Williams.

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Ritson-Williams, R., Arnold, S.N., Paul, V.J. et al. Larval settlement preferences of Acropora palmata and Montastraea faveolata in response to diverse red algae. Coral Reefs 33, 59–66 (2014). https://doi.org/10.1007/s00338-013-1113-2

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