Marine Biology

, 165:74 | Cite as

Microherbivores are significant grazers on Palau’s forereefs

  • Noam T. Altman-Kurosaki
  • Mark A. Priest
  • Yimnang Golbuu
  • Peter J. Mumby
  • Alyssa Marshell
Original paper

Abstract

Herbivory plays an important role in controlling benthic dynamics on coral reefs. The previous studies have highlighted the importance of grazing herbivorous fishes in removing algal turf biomass, but fewer studies have investigated the impact of invertebrate microherbivore grazing. This study examined the impact of microherbivore grazing in areas of high- and low-wave exposure on the forereefs of Palau, Micronesia, in June 2015. Experimental tiles were placed on open benthos, and in benthic and suspended herbivore exclusion cages at exposed and sheltered sites to partition the grazing impacts of microherbivores from fish grazers while examining the effect of exposure on algal turf productivity. Microherbivore grazing significantly impacted algal turf biomass, and this impact was greater in exposed sites than sheltered sites. Exposure did not significantly affect algal turf biomass on experimental tiles in the suspended exclusion cages. Surveys of microherbivore density revealed only Paguroidea (hermit crabs, especially of family Diogenidae) were more abundant at exposed sites than sheltered sites. Furthermore, tank trials of grazing rates showed diogenid hermit crabs removed over four times as much algal turf biomass as Columbellidae (marine gastropods), the second most abundant microherbivores. These results show that microherbivores are significant grazers on Palau’s forereefs, and may play an important role in maintaining reef resilience as reef health continues to decline worldwide. The significant role of invertebrate microherbivores in removing algal turf biomass should be investigated when considering the ecological role of herbivory on coral reefs.

Notes

Acknowledgements

The authors would like to thank the Princeton Environmental Institute’s Undergraduate Research fund for senior thesis research at Princeton University, the Mountlake Field Research Fund, and the Council on Science and Technology for financial support (grants to NAK). Additional funding was provided by the Australian Research Council’s Centre of Excellence for Coral Reef Studies (grant to PJM), the Australian Endeavour Award Postdoctoral Fellowship, and PADI Foundation Award (grants to AM) We also thank the Palau International Coral Reef Center for graciously hosting this study, Steve Lindfield for field assistance, Jessica Stella for help with invertebrate identification, and Stephen Pacala for additional guidance. We thank the reviewers for their comments, which improved our final manuscript.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflicts of interest.

Ethical approval

All applicable international, national, and/or institutional guidelines for the care and use of animals were followed.

Supplementary material

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Supplementary material 1 (PDF 3933 kb)
227_2018_3327_MOESM2_ESM.pdf (169 kb)
Supplementary material 2 (PDF 169 kb)
227_2018_3327_MOESM3_ESM.pdf (79 kb)
Supplementary material 3 (PDF 78 kb)
227_2018_3327_MOESM4_ESM.pdf (97 kb)
Supplementary material 4 (PDF 96 kb)

References

  1. Adey WH, Goertemiller T (1987) Coral reef algal turfs: master producers in nutrient poor seas. Phycologia 26:374–386CrossRefGoogle Scholar
  2. Adey WH, Steneck RS (1985) Highly productive eastern Caribbean reefs: synergistic effects of biological, chemical, physical and geological factors. Ecol Coral Reefs 3:163–187Google Scholar
  3. 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 414:91–105CrossRefGoogle Scholar
  4. Aronson RB, Precht WF (2000) Herbivory and algal dynamics on the coral reef at Discovery Bay, Jamaica. Limnol Oceanogr 45:251–255CrossRefGoogle Scholar
  5. Aronson RB, Precht WF, Toscano MA, Koltes KH (2002) The 1988 bleaching event and its aftermath on a coral reef in Belize. Mar Biol 141:435–447CrossRefGoogle Scholar
  6. Aronson RB, Macintyre IG, Wapnick CM, O’Neill MW (2004) Phase shifts, alternative states, and the unprecedented convergence of two reef systems. Ecology 85:1876–1891CrossRefGoogle Scholar
  7. Australian Bureau of Meteorology and CSIRO (2014) Palau. In: Climate variability, extremes and change in the western tropical Pacific: new science and updated country reports. Pacific-Australia climate change science and adaptation planning program technical report. Australian Bureau of Meteorology and Commonwealth Scientific and Industrial Research Organisation, Melbourne, Australia, pp 201–218Google Scholar
  8. Bejarano S, Jouffray JB, Chollet I, Allen R, Roff G, Marshell A, Steneck R, Ferse SCA, Mumby PJ (2017) The shape of success in a turbulent world: wave exposure filtering on coral reef herbivory. Funct Ecol 31:1312–1324.  https://doi.org/10.1111/1365-2435.12828 CrossRefGoogle Scholar
  9. Bellwood DR, Fulton CJ (2008) Sediment-mediated suppression of herbivory on coral reefs: decreasing resilience to rising sea-levels and climate change? Limnol Oceanogr 53:2695–2701CrossRefGoogle Scholar
  10. Bellwood DR, Hoey AS, Choat JH (2003) Limited functional redundancy in high diversity systems: resilience and ecosystem function on coral reefs. Ecol Lett 6:281–285CrossRefGoogle Scholar
  11. Birrell CL, McCook LJ, Willis BL (2005) Effects of algal turfs and sediment on coral settlement. Mar Pollut Bull 51:408–414CrossRefPubMedGoogle Scholar
  12. Bonaldo RM, Bellwood DR (2008) Size-dependent variation in the functional role of the parrotfish Scarus rivulatus on the Great Barrier Reef, Australia. Mar Ecol Prog Ser 360:237–244CrossRefGoogle Scholar
  13. Box SJ, Mumby PJ (2007) Effect of macroalgal competition on growth and survival of juvenile Caribbean corals. Mar Ecol Prog Ser 342:139–149CrossRefGoogle Scholar
  14. Brawley SH, Adey WH (1977) Territorial behavior of three spot damselfish (Eupomecentrus planifrons) increases reef algal biomass and productivity. Environ Biol Fishes 2:45–51CrossRefGoogle Scholar
  15. Brawley SH, Adey WH (1981) The effect of micrograzers on algal community structure in a coral reef microcosm. Mar Biol 61:167–177CrossRefGoogle Scholar
  16. Bronstein O, Loya Y (2014) Echinoid community structure and rates of herbivory and bioerosion on exposed and sheltered reefs. J Exp Mar Biol Ecol 456:8–17CrossRefGoogle Scholar
  17. Bruggemann JH, van Kessle AM, van Rooji JM, Breeman AM (1996) Bioerosion and sediment ingestion by the Caribbean parrotfish Scarus vetula and Sparisoma viride: implications of fish size, feeding mode and habitat use. Mar Ecol Prog Ser 134:59–71CrossRefGoogle Scholar
  18. Burkepile DE, Hay ME (2008) Herbivore species richness and feeding complementarity affect community structure and function on a coral reef. Proc Natl Acad Sci USA 105:16201–16206CrossRefPubMedPubMedCentralGoogle Scholar
  19. Burkepile DE, Hay ME (2010) Impact of herbivore identity on algal succession and coral growth on a Caribbean reef. PLoS ONE 5:e8963CrossRefPubMedPubMedCentralGoogle Scholar
  20. Carpenter RC (1986) Partitioning herbivory and its effects on coral reef algal communities. Ecol Monogr 56:345CrossRefGoogle Scholar
  21. Carpenter RC (1988) Mass mortality of a Caribbean sea urchin: immediate effects on community metabolism and other herbivores. Proc Natl Acad Sci USA 85:511–514CrossRefPubMedPubMedCentralGoogle Scholar
  22. Carpenter RC, Williams SL (1993) Effects of algal turf canopy height and microscale substratum topography on profiles of flow speed in a coral forereef environment. Limnol Oceanogr 38:687–694CrossRefGoogle Scholar
  23. Carpenter RC, Hackney JM, Adey WH (1991) Measurement of primary productivity and nitrogenase activity of coral reef algae in a chamber incorporating oscillatory flow. Limnol Oceanogr 36:40–49CrossRefGoogle Scholar
  24. Carpenter KE, Abrar M, Aeby G, Aronson RB, Banks S, Bruckner A, Chiriboga A, Cortes J, Delbeek JC, Devantier L, Edgar GJ, Edwards AJ, Fenner D, Guzman HM, Hoeksema BW, Hodgson G, Johan O, Licuanan WY, Livingstone SR, Lovell ER, Moore JA, Obura DO, Ochavillo D, Polidoro BA, Precht WF, Quibilan MC, Reboton C, Richards ZT, Rogers AD, Sanciangco J, Sheppard A, Sheppard C, Smith J, Stuart S, Turak E, Veron JEN, Wallace C, Weil E, Wood E (2008) One-third of reef-building corals face elevated extinction risk from climate change and local impacts. Science 321:560–563CrossRefPubMedGoogle Scholar
  25. Carreiro-Silva M, McClanahan TR (2001) Echinoid bioerosion and herbivory on Kenyan coral reefs: the role of protection from fishing. J Exp Mar Biol Ecol 262:133–153CrossRefPubMedGoogle Scholar
  26. Cernerhorsky NH, McClanahan TR, Babu I, Horsak M (2015) Small herbivores suppress algal accumulation on Agatti atoll, Indian Ocean. Coral Reefs 34:1023–1035CrossRefGoogle Scholar
  27. Choat JH (1991) The biology of herbivorous fishes on coral reefs. In: Sale PF (ed) The ecology of fishes on coral reefs. Academic Press Inc, San Diego, pp 120–155Google Scholar
  28. Clarke KR (1993) Non parametric multivariate analysis of changes in community structure. Aust J Ecol 18:117–143CrossRefGoogle Scholar
  29. Clarke KR, Gorley RN (2006) PRIMERv6: user manual/tutorial. Primer-E, Plymouth Marine Laboratory, PlymouthGoogle Scholar
  30. Coen LD (1988a) Herbivory by Caribbean majid crabs: feeding ecology and plant susceptibility. J Exp Mar Biol Ecol 122:257–276CrossRefGoogle Scholar
  31. Coen LD (1988b) Herbivory by crabs and the control of algal epibionts on Caribbean host corals. Oecologia 75:198–203CrossRefPubMedGoogle Scholar
  32. Coen LD, Tanner CE (1989) Morphological variation and differential susceptibility to herbivory in the tropical brown alga Lobophora variegata. Mar Ecol Prog Ser 54:287–298CrossRefGoogle Scholar
  33. Cronin G, Paul VJ, Hay ME, Renical W (1997) Are tropical herbivores more resistant than temperate herbivores to seaweed chemical defences? Diterpenoid metabolites from Dictyota acutiloba as feeding deterrents for tropical versus temperate fishes and urchins. J Chem Ecol 23:289–302CrossRefGoogle Scholar
  34. Doropoulos C, Ward S, Marshell A, Diaz-Pulido G, Mumby PJ (2012) Interactions among chronic and acute impacts on coral recruits: the importance of size-escape thresholds. Ecology 93:2131–2138CrossRefPubMedGoogle Scholar
  35. Doropoulos C, Roff G, Zupan M, Nestor V, Isechal AL, Mumby PJ (2014) Reef-scale failure of coral settlement following typhoon disturbance and macroalgal bloom in Palau, Western Pacific. Coral Reefs 33:613–623CrossRefGoogle Scholar
  36. Doropoulos C, Roff G, Bozec Y, Zupan M, Werminghausen J, Mumby PJ (2016) Characterizing the ecological trade-offs throughout the early ontogeny of coral recruitment. Ecol Monogr 86:20–44Google Scholar
  37. Duffy JE, Hay ME (1990) Seaweed adaptations to herbivory. Bioscience 40:368–375CrossRefGoogle Scholar
  38. Dumas P, Kulbicki M, Chifflet S, Fichez R, Ferraris J (2007) Environmental factors influencing urchin spatial distributions on disturbed coral reefs (New Caledonia, South Pacific). J Exp Mar Biol Ecol 344:88–100CrossRefGoogle Scholar
  39. Dunn RP, Altieri AH, Miller K, Yeager M, Hovel KA (2017) Coral identity and structural complexity drive habitat associations and demographic processes for an increasingly important Caribbean herbivore. Mar Ecol Prog Ser 577:34–47CrossRefGoogle Scholar
  40. Fang JKH, Schönberg CHL, Kline DI, Hoegh-Guldberg O, Dove S (2012) Methods to quantify components of the excavating sponge Cliona orientalis Thiele, 1900. Mar Ecol 34:193–206CrossRefGoogle Scholar
  41. Foster NL, Box SJ, Mumby PJ (2008) Competitive effects of macroalgae on the fecundity of the reef-building coral Montastraea annularis. Mar Ecol Prog Ser 367:143–152CrossRefGoogle Scholar
  42. Fox RJ, Bellwood DR (2008) Direct versus indirect methods of quantifying herbivore grazing impact on a coral reef. Mar Biol 154:325–334CrossRefGoogle Scholar
  43. Froese R, Pauly D (2016) Fishbase. http://www.fishbase.org/. Accessed 27 July 2015
  44. Fulton CJ, Bellwood DR (2005) Wave-induced water motion and the functional implications for coral reef fish assemblages. Limnol Oceanogr 50:255–264CrossRefGoogle Scholar
  45. Goatley CHR, Bellwood DR (2012) Sediment suppresses herbivory across a coral reef depth gradient. Biol Lett 8:1016–1018CrossRefPubMedPubMedCentralGoogle Scholar
  46. Goatley CHR, Bonaldo RM, Fox RJ, Bellwood DR (2016) Sediments and herbivory as sensitive indicators of coral reef degradation. Ecol Soc 21:29CrossRefGoogle Scholar
  47. Harris JL, Lewis LS, Smith JE (2015) Quantifying scales of spatial variability in algal turf assemblages on coral reefs. Mar Ecol Prog Ser 532:41–57CrossRefGoogle Scholar
  48. Hatcher BG, Larkum AWD (1983) An experimental analysis of factors controlling the standing crop of the epilithic algal community on a coral reef. J Exp Mar Biol Ecol 69:61–84CrossRefGoogle Scholar
  49. Hay ME (1997) The ecology and evolution of seaweed-herbivore interactions on coral reefs. Coral Reefs 16:S67–S76CrossRefGoogle Scholar
  50. Hixon MA, Brostoff WN (1996) Succession and herbivory: effects of differential fish grazing on Hawaiian coral reef algae. Eol Monogr 66:67–90CrossRefGoogle Scholar
  51. Hoey AS, Bellwood DR (2009) Limited functional redundancy in a high diversity system: single species dominates key ecological process on coral reefs. Ecosystems 12:1316–1328CrossRefGoogle Scholar
  52. Hughes TP, Reed DC, Boyle M (1987) Herbivory on coral reefs: community structure following mass mortalities of sea urchins. J Exp Mar Biol Ecol 113:39–59CrossRefGoogle Scholar
  53. 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 17:360–365CrossRefPubMedGoogle Scholar
  54. Idjadi JA, Edmunds PJ (2006) Scleractinian corals as facilitators for other invertebrates on a Caribbean reef. Mar Ecol Prog Ser 319:117–127CrossRefGoogle Scholar
  55. Johansson CL, van de Leemput IA, Depczynski M, Hoey AS, Bellwood DR (2013) Key herbivores reveal limited functional redundancy on inshore coral reefs. Coral Reefs 32:963–972CrossRefGoogle Scholar
  56. Jyoti J, Awatshi M (2013) Factors affecting algal growth. In: Kumar S, Tyagi SK (eds) Recent advances in bioenergy research, vol 2. Sardar Swaran Singh National Institute of Renewable Energy, Kapurthala, pp 315–324Google Scholar
  57. Klumpp DW, McKinnon AD (1989) Temporal and spatial patterns in primary production of a coral-reef epilithic algal community. J Exp Mar Biol Ecol 131:1–22CrossRefGoogle Scholar
  58. Klumpp DW, Polunin NVC (1989) Partitioning among grazers of food resources within damselfish territories on a coral reef. J Exp Mar Biol Ecol 125:145–169CrossRefGoogle Scholar
  59. Klumpp DW, Pulfrich A (1989) Trophic significance of herbivorous macroinvertebrates on the central Great Barrier Reef. Coral Reefs 8:135–144CrossRefGoogle Scholar
  60. Kohler KE, Gill SM (2006) Coral Point Count with Excel extensions (CPCe): a visual basic program for the determination of coral and substrate coverage using random point count methodology. Comput Geosci 32:1259–1269CrossRefGoogle Scholar
  61. Kuempel CD, Altieri AH (2017) The emergent role of small-bodied herbivores in pre-empting phase shifts on degraded coral reefs. Sci Rep 7:39670.  https://doi.org/10.1038/srep39670 CrossRefPubMedPubMedCentralGoogle Scholar
  62. Kulbicki M, Guillemot N, Amand M (2005) A general approach to length-weight relationships for New Caledonian lagoon fishes. Cybium 29:235–252Google Scholar
  63. Larned ST, Atkinson MJ (1997) Effects of water velocity on NH4 and PO4 uptake and nutrient-limited growth in the macroalga Dictyosphaeria cavernosa. Mar Ecol Prog Ser 157:295–302CrossRefGoogle Scholar
  64. Ledlie MH, Graham NAJ, Bythell JC, Wilson SK, Jennings S, Polunin SVC, Hardcastle J (2007) Phase shifts and the role of herbivory in the resilience of coral reefs. Coral Reefs 26:641–653CrossRefGoogle Scholar
  65. Marshell A, Mumby P (2015) The role of surgeonfish (Acanthuridae) in maintaining algal turf biomass on coral reefs. J Exp Mar Biol Ecol 473:152–160CrossRefGoogle Scholar
  66. Mathieson AC, Fralick RA, Burns R, Flahive W (1971) Comparative studies of subtidal vegetation in the Virgin Islands and New England coastlines. In: Miller JW, VanDerwalker JG, Waller RA (eds) Scientists in the sea. Department of the Interior, Washington, DC, pp 106–129Google Scholar
  67. McClanahan TR (1999) Predation and the control of the sea urchin Echinometra viridis and fleshy algae in the patch reefs of Glovers Reef, Belize. Ecosystems 2:511–523CrossRefGoogle Scholar
  68. Mumby PJ, Hedley JD, Zychaluk K, Harborne AR, Blackwell PG (2006a) Revisiting the catastrophic die-off of the urchin Diadema antillarum on Caribbean coral reefs: fresh insights on resilience from a simulation model. Ecol Model 196:131–148CrossRefGoogle Scholar
  69. 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 (2006b) Fishing, trophic cascades, and the process of grazing on coral reefs. Science 311:98–101.  https://doi.org/10.1126/science.1121129 CrossRefPubMedGoogle Scholar
  70. Mumby PJ, Steneck RS, Adjeroud M, Arnold SN (2015) High resilience masks underlying sensitivity to algal phase shifts of Pacific coral reefs. Oikos 125:644–655CrossRefGoogle Scholar
  71. Muthiga N, McClanahan TR (1987) Population changes of sea urchin (Echinometra mathaei) on an exploited fringing reef. Afr J Ecol 25:1–8Google Scholar
  72. Nelson HR, Kuempel CD, Altieri AH (2016) The resilience of reef invertebrate biodiversity to coral mortality. Ecosphere 7:e01399.  https://doi.org/10.1002/ecs2.1399 CrossRefGoogle Scholar
  73. Netchy K, Hallock P, Lunz KS, Daly KL (2015) Epibenthic mobile invertebrate diversity organized by coral habitat in Florida. Mar Biodivers 46:1–13Google Scholar
  74. Nystrom M, Folke C (2001) Spatial resilience on coral reefs. Ecosystems 4:406–417CrossRefGoogle Scholar
  75. Pandolfi JM, Bradbury RH, Sala E, Hughes TP, Bjorndal KA, Cooke RG, McArdle D, McClenachan L, Newman MJ, Paredes G (2003) Global trajectories of the long-term decline of coral reef ecosystems. Science 301:955–958CrossRefPubMedGoogle Scholar
  76. Quan-Young LI, Espinoza-Avalos J (2006) Reduction of zooxanthellae density, chlorophyll a concentration, and tissue thickness of the coral Montastraea faveolata (Scelractinia) when competing with mixed turf algae. Limnol Oceanogr 51:1159–1166CrossRefGoogle Scholar
  77. Rasher DB, Hay ME (2010) Chemically rich seaweeds poison corals when not controlled by herbivores. Proc Natl Acad Sci USA 107:9683–9688CrossRefPubMedPubMedCentralGoogle Scholar
  78. Ritson-Williams R, Arnold SN, Paul VJ, Steneck RS (2014) Larval settlement preferences of Acropora palmata and Montastraea faveolata in response to diverse red algae. Coral Reefs 33:59–66CrossRefGoogle Scholar
  79. Russ G (1984) 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 20:23–34CrossRefGoogle Scholar
  80. Russ GR (2003) Grazer biomass correlates more strongly with production than with biomass of algal turfs on a coral reef. Coral Reefs 22:63–67Google Scholar
  81. Sammarco PW (1982) Effects of grazing by Diadema antillarum Philippi (Echinodermata: Echinoidea) on algal diversity and community structure. J Exp Mar Biol Ecol 65:83–105CrossRefGoogle Scholar
  82. Sangil C, Guzman HM (2016) Assessing the herbivore role of the sea-urchin Echinometra viridis: keys to determine the structure of communities in disturbed coral reefs. Mar Environ Res 120:202–213CrossRefPubMedGoogle Scholar
  83. Schlichting H (1979) Boundary-layer theory. McGraw-Hill, New YorkGoogle Scholar
  84. Schupp PJ, Paul VJ (1994) Calcium carbonate and secondary metabolites in tropical seaweeds: variable effects on herbivorous fishes. Ecology 75:1172–1185CrossRefGoogle Scholar
  85. Steneck RS (1983) Escalating herbivory and resulting adaptive trends in calcareous algal crusts. Paleobiology 9:44–61CrossRefGoogle Scholar
  86. Steneck RS (1988) Herbivory on coral reefs: a synthesis. In: Proceedings of the 6th international coral reef symposium, vol 1, pp 37–49Google Scholar
  87. Steneck RS, Dethier MN (1994) A functional group approach to the structure of algal-dominated communities. Oikos 69:476–498CrossRefGoogle Scholar
  88. Steneck RS, Arnold SN, Mumby PJ (2014) Experiment mimics fishing on parrotfish: insights on coral reef recovery and alternative attractors. Mar Ecol Prog Ser 506:115–127CrossRefGoogle Scholar
  89. Tanner JE (1995) Competition between scleractinian corals and macroalgae: an experimental investigation of coral growth, survival and reproduction. J Exp Mar Biol Ecol 190:151–168CrossRefGoogle Scholar
  90. Thomas FIM, Atkinson MJ (1997) Ammonium uptake by coral reefs: effects of water velocity and surface roughness on mass transfer. Limnol Oceanogr 42:81–88CrossRefGoogle Scholar
  91. Vermeij MJA, Moorselaar IV, Engelhard S, Hornlein C, Vonk SM, Visser PM (2010) The effects of nutrient enrichment and herbivore abundance on the ability of turf algae to overgrow coral in the Caribbean. PLoS ONE 5(12):e14312.  https://doi.org/10.1371/journal.pone.0014312 CrossRefPubMedPubMedCentralGoogle Scholar
  92. Vogel S (1984) Drag and flexibility in sessile organisms. Integr Comp Biol 24:37–44Google Scholar
  93. 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 41:279–309Google Scholar

Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2018

Authors and Affiliations

  • Noam T. Altman-Kurosaki
    • 1
    • 2
    • 3
  • Mark A. Priest
    • 4
    • 5
  • Yimnang Golbuu
    • 4
  • Peter J. Mumby
    • 5
  • Alyssa Marshell
    • 5
    • 6
  1. 1.Department of Ecology and Evolutionary BiologyPrinceton UniversityPrincetonUSA
  2. 2.Princeton Environmental InstitutePrinceton UniversityPrincetonUSA
  3. 3.Hawaii Institute of Marine BiologyUniversity of Hawaii at ManoaKaneoheUSA
  4. 4.Palau International Coral Reef CentreKororPalau
  5. 5.Marine Spatial Ecology Lab, Australian Research Council Centre of Excellence for Coral Reef Studies, School of Biological SciencesUniversity of QueenslandBrisbaneAustralia
  6. 6.Marine Ecology Lab Oman, Department of Marine Science and Fisheries, College of Agriculture and Marine ScienceSultan Qaboos UniversityMuscatOman

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