Abstract
The study of bioerosion, a widespread process greatly impacting reef biodiversity, structural complexity, and sediment production, has largely focused on shallow-water reefs with no review of this process in deeper environments. In this first synthesis of bioerosion literature for mesophotic reefs (subtropical and tropical ecosystems in low-light conditions at depths of ~30 to 150 m), we show that the distribution of key bioeroder taxa, their abundances, and overall bioerosion rates are considerably different on mesophotic reefs compared to their shallow-water counterparts. In particular, carbonate grazing and phototrophic microboring rates decline with depth from shallow to mesophotic reefs. In the absence of significant erosive action by grazers, sponges are hypothesized as the primary long-term bioeroders on lower mesophotic reefs (60–150 m) and possibly on some upper mesophotic reefs (30–60 m). Given these factors, we postulate that mesophotic reef substrates experience slower bioerosion rates and lose less carbonate than shallower reefs over the same timeframe. This likely stems from differences in photosynthetically active radiation and other factors such as temperature, sedimentation, bioeroder food abundance and quality, substrate characteristics, and exposure time for bioerosion. There is a critical need to document mesophotic bioeroders via taxonomic inventories, as well as quantify their bioerosion rates across mesophotic depths in terms of specific bioeroder guilds using experimental substrates. These data will aid management efforts to maintain positive net carbonate budgets on mesophotic reefs, ensuring that sufficient three-dimensional structure is available to support biodiversity at mesophotic depths.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Alwany MA, Thaler E, Stachowitsch M (2009) Parrotfish bioerosion on Egyptian Red Sea reefs. J Exp Mar Biol Ecol 371:170–176
Andradi-Brown DA, Gress E, Wright G et al (2016) Reef fish community biomass and trophic structure changes across shallow to upper-mesophotic reefs in the Mesoamerican Barrier Reef, Caribbean. PLoS ONE 11:e0156641
Aponte NE, Ballantine DL (2001) Depth distribution of algal species on the deep insular fore reef at Lee Stocking Island, Bahamas. Deep-Sea Res I Oceanogr Res Pap 48:2185–2194
Appeldoorn R, Ballantine D, Bejarano I et al (2016) Mesophotic coral ecosystems under anthropogenic stress: a case study at Ponce, Puerto Rico. Coral Reefs 35(1):63–75
Asher J, Williams ID, Harvey ES (2017) Mesophotic depth gradients impact reef fish assemblage composition and functional group partitioning in the main Hawaiian Islands. Front Mar Sci 4:98
Bak RPM (1976) The growth of coral colonies and the importance of crustose coralline algae and burrowing sponges in relation with carbonate accumulation. Neth J Sea Res 10(3):285–337
Baker PA, Weber JN (1975) Coral growth rate: variation with depth. Earth Planet Sci Lett 27(1):57–61
Baker EK, Puglise KA, Harris PT (eds) (2016) Mesophotic coral ecosystems – a lifeboat for coral reefs? United Nations Environment Programme and GRID, Nairobi, 98p
Bejarano I, Appeldoorn RS, Nemeth M (2014) Fishes associated with mesophotic coral ecosystems in La Parguera, Puerto Rico. Coral Reefs 33(2):313–328
Bellwood DR, Choat JH (1990) A functional analysis of grazing in parrotfishes (family Scaridae): the ecological implications. Environ Biol Fish 28(1–4):189–214
Bonaldo RM, Hoey AS, Bellwood DR (2014) The ecosystem roles of parrotfishes on tropical reefs. In: Hughes RN, Hughes DJ, Smith IP (eds) Oceanography and marine biology: an annual review. CRC Press, Boca Raton, pp 81–132
Bongaerts P, Ridgway T, Sampayo EM et al (2010) Assessing the ‘Deep Reef Refugia’ hypothesis: focus on Caribbean reefs. Coral Reefs 29(2):309–327
Bosscher H, Schlager W (1992) Computer simulation of reef growth. Sedimentology 39(3):503–512
Bouchon-Navaro Y, Harmelin-Vivien ML (1981) Quantitative distribution of herbivorous reef fishes in the Gulf of Aqaba (Red Sea). Mar Biol 63(1):79–86
Bridge TCL, Luiz OJ, Coleman RR et al (2016) Ecological and morphological traits predict depth-generalist fishes on coral reefs. Proc R Soc Lond [Biol] 283:20152332
Brokovich E, Ayalon I, Einbinder S et al (2010) Grazing pressure on coral reefs decreases across a wide depth gradient in the Gulf of Aqaba, Red Sea. Mar Ecol Prog Ser 399:69–80
Bruggemann JH, van Kessel AM, van Rooij JM et al (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 134:59–71
Budd DA, Perkins RD (1980) Bathymetric zonation and paleoecological significance of microborings in Puerto Rican shelf and slope sediments. J Sediment Res 50(3):881–903
Cardoso SC, Soares MC, Oxenford HA et al (2009) Interspecific differences in foraging behaviour and functional role of Caribbean parrotfish. Mar Biodivers Rec 2:1–6
Chazottes V, Le Campion-Alsumard T, Peyrot-Clausade M (1995) Bioerosion rates on coral reefs: interactions between macroborers, microborers and grazers (Moorea, French Polynesia). Palaeogeogr Palaeoclimatol Palaeoecol 113(2–4):189–198
Chazottes V, Le Campion-Alsumard T, Peyrot-Clausade M et al (2002) The effects of eutrophication-related alterations to coral reef communities on agents and rates of bioerosion (Reunion Island, Indian Ocean). Coral Reefs 21(4):375–390
Chazottes V, Cabioch G, Golubic S et al (2009) Bathymetric zonation of modern microborers in dead coral substrates from New Caledonia – implications for paleodepth reconstructions in Holocene corals. Palaeogeogr Palaeoclimatol Palaeoecol 280(3–4):456–468
Clements KD, German DP, Piché J et al (2016) Integrating ecological roles and trophic diversification on coral reefs: multiple lines of evidence identify parrotfishes as microphages. Biol J Linn Soc 120:729–751
Dennis GD, Bright TJ (1988) Reef fish assemblages on hard banks in the northwestern Gulf of Mexico. Bull Mar Sci 43:280–307
Dullo W, Gektidis M, Golubic S et al (1995) Factors controlling Holocene reef growth: an interdisciplinary approach. Facies 32(1):145–188
Färber C, Wisshak M, Pyko I et al (2015) Effects of water depth, seasonal exposure, and substrate orientation on microbial bioerosion in the Ionian Sea (Eastern Mediterranean). PLoS ONE 10:e0126495
Feitoza BM, Rosa RS, Rocha LA (2005) Ecology and zoogeography of deep-reef fishes in northeastern Brazil. Bull Mar Sci 76:725–742
Friedlander AM, Sandin SA, DeMartini EE et al (2010) Spatial patterns of the structure of reef fish assemblages at a pristine atoll in the central Pacific. Mar Ecol Prog Ser 410:219–231
Fukunaga A, Kosaki RK, Wagner D et al (2016) Structure of mesophotic reef fish assemblages in the Northwestern Hawaiian Islands. PLoS ONE 11:e0157861
García-Sais JR (2010) Reef habitats and associated sessile-benthic and fish assemblages across a euphotic-mesophotic depth gradient in Isla Desecheo, Puerto Rico. Coral Reefs 29(2):277–288
Gektidis M, Dubinsky Z, Goffredo S (2007) Microendoliths of the shallow euphotic zone in open and shaded habitats at 30°N–Eilat, Israel–paleoecological implications. Facies 53(1):43–55
Glynn PW, Manzello DP (2015) Bioerosion and coral reef growth: a dynamic balance. In: Birkeland C (ed) Coral reefs in the Anthropocene. Springer, Dordrecht, pp 67–97
Golubic SS, Perkins RD, Lukas KJ (1975) Boring microorganisms and microborings in carbonate substrates. In: Frey RW (ed) Study of trace fossils. Springer, Berlin, pp 229–259
Goreau TF, Hartman WD (1963) Control of coral reefs by boring sponges. In: Sognnaes RF (ed) Mechanisms of hard tissue destruction. AAAS Publishing, Washington, DC, pp 25–54
Greenstein BJ, Pandolfi JM (2003) Taphonomic alteration of reef corals: effects of reef environment and coral growth form II: the Florida Keys. Palaios 18:495–509
Grigg RW (2006) Depth limit for reef building corals in the Auʻau Channel, S.E. Hawaii. Coral Reefs 25(1):77–84
Günther A (1990) Distribution and bathymetric zonation of shell-boring endoliths in recent reef and shelf environments: Cozumel, Yucatan (Mexico). Facies 22(1):233–261
Hassan M (1998) Modification of carbonate substrata by bioerosion and bioaccretion on coral reefs of the Red Sea. Shaker Verlag, Aachen (thesis)
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(1):61–84
Heindel K, Westphal H, Wisshak M (2009) Data report: bioerosion in the reef framework, IODP Expedition 310 off Tahiti (Tiarei, Maraa, and Faaa sites). In: Camoin GF, Iryu Y, McInroy DB, Expedition 310 Scientists (eds) Proceedings of the Integrated Ocean Drilling Program. Integrated Ocean Drilling Program Management International, Washington, DC
Hernández-Ballesteros LM, Elizalde-Rendón EM, Carballo JL et al (2013) Sponge bioerosion on reef-building corals: dependent on the environment or on skeletal density? J Exp Mar Biol Ecol 441:23–27
Highsmith RC (1981) Coral bioerosion: damage relative to skeletal density. Am Nat 117(2):193–198
Hinderstein LM, Marr JCA, Martinez FA et al (2010) Theme section on “Mesophotic Coral Ecosystems: Characterization, Ecology, and Management.” Coral Reefs 29(2):247–251
Hoskin CM, Reed JK, Mook DH (1986) Production and off-bank transport of carbonate sediment, Black Rock, southwest Little Bahama Bank. Mar Geol 73(1–2):125–144
Hubbard DK (2009) Depth and species-related patterns of Holocene reef accretion in the Caribbean and Western Atlantic: a critical assessment of existing models. In: Swart PK, Eberli GP, McKenzie JA (eds) Perspectives in carbonate geology: a tribute to the career of Robert Nathan Ginsburg. International Association of Sedimentologists Special Publication. Blackwell, Oxford, pp 1–18
Hubbard DK, Scaturo D (1985) Growth rates of seven species of scleractinian corals from Cane Bay and Salt River, St. Croix, USVI. Bull Mar Sci 36(2):325–338
Hubbard DK, Miller AI, Scaturo D (1990) Production and cycling of calcium carbonate in a shelf-edge reef system (St. Croix, U.S. Virgin Islands): applications to the nature of reef systems in the fossil record. J Sediment Res 60(3):335–360
Hughes TP (1987) Skeletal density and growth form of corals. Mar Ecol Prog Ser 35:259–266
Huston M (1985) Variation in coral growth rates with depth at Discovery Bay, Jamaica. Coral Reefs 4(1):19–25
Hutchings PA (2011) Bioerosion. In: Hopley D (ed) Encyclopedia of modern coral reefs: structure, form and process. Springer, Dordrecht, pp 139–156
James NP, Ginsburg RN (1979) The seaward margin of Belize barrier and atoll reefs: morphology, sedimentology, organism distribution and late Quaternary history. Blackwell Scientific Publishing Ltd., Oxford, 204p
Kahle D, Wickham H (2013) ggmap: spatial visualization with ggplot 2. R J 5:144–161
Kahng SE, García-sais JR, Spalding HL et al (2010) Community ecology of mesophotic coral reef ecosystems. Coral Reefs 29(2):255–275
Kane C, Kosaki RK, Wagner D (2014) High levels of mesophotic reef fish endemism in the northwestern Hawaiian Islands. Bull Mar Sci 90:693–703
Kiene WE (1985) Biological destruction of experimental coral substrates at Lizard Island (Great Barrier Reef, Australia). In: Harmelin Vivien M, Salvat B (eds) Proceedings of the 5th International Coral Reef Symposium, vol 5. Tahiti, pp 339–344 Miscellaneous Paper (A)
Kiene WE, Hutchings PA (1993) Long-term bioerosion of experimental coral substrates from Lizard Island, Great Barrier Reef. In: Richmond RH (ed) Proceedings of the 7th International Coral Reef Symposium, vol 1. University of Guam Press, UOG Station, Guam, pp 397–403
Kiene WE, Hutchings PA (1994) Bioerosion experiments at Lizard Island, Great Barrier Reef. Coral Reefs 13(2):91–98
Lesser MP, Slattery M (2011) Phase shift to algal dominated communities at mesophotic depths associated with lionfish (Pterois volitans) invasion on a Bahamian coral reef. Biol Invasions 13(8):1855–1868
Lesser MP, Slattery M, Leichter JJ (2009) Ecology of mesophotic reefs. J Exp Mar Bio Ecol 375:1-8
Lewis SM, Wainwright PC (1985) Herbivore abundance and grazing intensity on a Caribbean coral reef. J Exp Mar Biol Ecol 87(3):215–228
Liddell WD, Ohlhorst SL (1986) Changes in benthic community composition following the mass mortality of Diadema at Jamaica. J Exp Mar Biol Ecol 95(3):271–278
Liddell WD, Ohlhorst SL (1988) Hard substrata community patterns, 1–120 m, north Jamaica. Palaios 3(4):413–423
Liddell WD, Ohlhorst SL, Boss SK (1984) Community patterns on the Jamaican fore-reef (15–56 m). Paleontol Am 54:385–389
Lindfield SJ, Harvey ES, Halford AR et al (2016) Mesophotic depths as refuge areas for fishery-targeted species on coral reefs. Coral Reefs 35(1):125–137
Lough JM, Cooper TF (2011) New insights from coral growth band studies in an era of rapid environmental change. Earth-Sci Rev 108(3–4):170–184
MacGeachy JK (1977) Factors controlling sponge boring in Barbados reef corals. In: Taylor DL (ed) Proceedings of the 3rd International Coral Reef Symposium, vol 2: Geology. Rosenstiel School of Marine and Atmospheric Science, Miami, pp 477–483
MacGeachy JK, Stearn CW (1976) Boring by macroorganisms in the coral Montastrea annularis on Barbados reefs. Int Rev Hydrobiol Hydrogr 61(6):715–745
Maher RL, Johnston MA, Brandt ME, Smith TB, Correa AMS (2018) Depth and coral cover drive the distribution of a coral macroborer across two reef systems. PLoS ONE 13(6):e0199462
Moore and Shedd (1977) Effective rates of sponge bioerosion as a function of carbonate production. In: Taylor DL (ed) Proceedings of the 3rd International Coral Reef Symposium, vol 2: Geology. Rosenstiel School of Marine and Atmospheric Science, Miami, pp 499–505
Morrison D (1988) Comparing fish and urchin grazing in shallow and deeper coral reef algal communities. Ecology 69(5):1367–1382
Mumby PJ (2009) Herbivory versus corallivory: are parrotfish good or bad for Caribbean coral reefs? Coral Reefs 28(3):683–690
Muñoz RC, Buckel CA, Whitfield PE et al (2017) Conventional and technical diving surveys reveal elevated biomass and differing fish community composition from shallow and upper mesophotic zones of a remote United States coral reef. PLoS ONE 12:e0188598
Nemeth RS, Smith TB, Blondeau J et al (2008) Characterization of deep water reef communities within the Marine Conservation District, St. Thomas, U.S. Virgin Islands. Caribbean Fisheries Management Council Final Report 3349, 82 p
Neumann AC (1966) Observations on coastal erosion in Bermuda and measurements of the boring rate of the sponge, Cliona lampa. Limnol Oceanogr 11:92–108
Ogden JC, Lobel PS (1978) The role of herbivorous fishes and urchins in coral reef communities. Environ Biol Fish 3(1):49–63
Perry CT (1998) Macroborers within coral framework at Discovery Bay, north Jamaica: species distribution and abundance, and effects on coral preservation. Coral Reefs 17(3):277–287
Perry CT (1999) Reef framework preservation in four contrasting modern reef environments, Discovery Bay, Jamaica. J Coast Res 15(3):796–812
Perry CT, Harborne AR (2016) Bioerosion on modern reefs: impacts and responses under changing ecological and environmental conditions. In: Hubbard DK, Rogers CS, Lipps JH, Stanley GD Jr (eds) Coral reefs at the crossroads. Springer, Dordrecht, pp 69–101
Perry CT, Hepburn LJ (2008) Syn-depositional alteration of coral reef framework through bioerosion, encrustation and cementation: taphonomic signatures of reef accretion and reef depositional events. Earth-Sci Rev 86(1–4):106–144
Perry CT, Macdonald IA (2002) Impacts of light penetration on the bathymetry of reef microboring communities: implications for the development of microendolithic trace assemblages. Palaeogeogr Palaeoclimatol Palaeoecol 186(1–2):101–113
Perry CT, Edinger EN, Kench PS et al (2012) Estimating rates of biologically driven coral reef framework production and erosion: a new census-based carbonate budget methodology and applications to the reefs of Bonaire. Coral Reefs 31(3):853–868
Perry CT, Murphy GN, Kench PS et al (2013) Caribbean-wide decline in carbonate production threatens coral reef growth. Nat Commun 4:1402
Perry CT, Murphy GN, Kench PS et al (2014) Changing dynamics of Caribbean reef carbonate budgets: emergence of reef bioeroders as critical controls on present and future reef growth potential. Proc R Soc B Biol Sci 281(1796):20142018
Pinheiro HT, Mazzei E, Moura RL et al (2015) Fish biodiversity of the Vitória-Trindade Seamount Chain, southwestern Atlantic: an updated database. PLoS ONE 10:e0118180
Pinheiro HT, Goodbody-Gringley G, Jessup ME et al (2016) Upper and lower mesophotic coral reef fish communities evaluated by underwater visual censuses in two Caribbean locations. Coral Reefs 35(1):139–151
Reaka-Kudla ML, Feingold JS, Glynn W (1996) Experimental studies of rapid bioerosion of coral reefs in the Galápagos Islands. Coral Reefs 15(2):101–107
Rosa MR, Alves AC, Medeiros DV et al (2016) Mesophotic reef fish assemblages of the remote St. Peter and St. Paul’s Archipelago, Mid-Atlantic Ridge, Brazil. Coral Reefs 35(1):113–123
Rose CS, Risk MJ (1985) Increase in Cliona delitrix infestation of Montastrea cavernosa heads on an organically polluted portion of the Grand Cayman fringing reef. Mar Ecol 6(4):345–363
Schlager W (1981) The paradox of drowned reefs and carbonate platforms. Geol Soc Am Bull 92(4):197–211
Schönberg CHL (2002) Substrate effects on the bioeroding demosponge Cliona orientalis. 1. Bioerosion rates. Mar Ecol 23(4):313–326
Schönberg CHL, Fang JKH, Carballo JL (2017a) Bioeroding sponges and the future of coral reefs. In: Carballo J, Bell J (eds) Climate change, ocean acidification and sponges: impacts across multiple levels of organization. Springer, Cham, pp 179–372
Schönberg CHL, Fang JKH, Carreiro-Silva M et al (2017b) Bioerosion: the other ocean acidification problem. ICES J Mar Sci 74(1):895–925
Sherman C, Locker SD, Webster JM et al (2019) Geology and geomorphology. In: Loya Y, Puglise KA, Bridge TCL (eds) Mesophotic coral ecosystems. Springer, New York, pp 849–878
Smith TB, Kadison E, Henderson L et al (2012) The United States Virgin Islands Territorial Coral Reef Monitoring Program, 2011 Annual Report. University of the Virgin Islands, United States Virgin Islands, 243 p
Smith TB, Ennis RS, Kadison E et al (2015) The United States Virgin Islands Territorial Coral Reef Monitoring Program, year 15 Annual Report. Version 1. University of the Virgin Islands, United States Virgin Islands, 288 p
Steneck RS (1983) Quantifying herbivory on coral reefs: just scratching the surface and still biting off more than we can chew. In: Reaka ML (ed) The ecology of deep and shallow coral reefs. Symposia Series for Undersea Research, Office of Undersea Research, NOAA, Rockville, MD, pp 103–111
Tapanila L, Hutchings P (2012) Reefs and mounds. In: Knaust D, Bromley RG (eds) Developments in sedimentology: trace fossils as indicators of sedimentary environments. vol 64. Elsevier, Amsterdam, pp 751–775
Thresher RE, Colin PL (1986) Trophic structure, diversity and abundance of fishes of the deep reef (30–300 m) at Enewetak, Marshall Islands. Bull Mar Sci 38:253–272
Toro-Farmer G, Cantera Kintz JR, Londoño-Cruz E et al (2004) Patrones de distribución y tasas de bioerosión del erizo Centrostephanus coronatus (Diadematoida: Diadematidae), en el arrecife de Playa Blanca, Pacífico Colombiano. Rev Biol Trop 52:67–76
Tribollet A (2008) The boring microflora in modern coral reef ecosystems: a review of its roles. In: Wisshak M, Tapanila L (eds) Current developments in bioerosion. Springer, Berlin/Heidelberg, pp 67–94
Tribollet A, Golubic S (2005) Cross-shelf differences in the pattern and pace of bioerosion of experimental carbonate substrates exposed for 3 years on the northern Great Barrier Reef, Australia. Coral Reefs 24(3):422–434
Tribollet A, Golubic S (2011) Reef bioerosion: agents and processes. In: Dubinsky Z, Stambler N (eds) Coral reefs: an ecosystem in transition. Springer, Dordrecht, pp 435–449
Tribollet A, Decherf G, Hutchings P et al (2002) Large-scale spatial variability in bioerosion of experimental coral substrates on the Great Barrier Reef (Australia): importance of microborers. Coral Reefs 21(4):424–432
Tribollet A, Radtke G, Golubic S (2011) Bioerosion. In: Reitner J, Thiel V (eds) Encyclopedia of geobiology. Springer Netherlands, Dordrecht, pp 117–134
van den Hoek C, Breeman AM, Bak RPM et al (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 Curaçao, Netherlands Antilles. Aquat Bot 5:1–46
Vogel K, Gektidis M, Golubic S et al (2000) Experimental studies on microbial bioerosion at Lee Stocking Island, Bahamas, and One Tree Island, Great Barrier Reef, Australia: implications for paleoecological reconstructions. Lethaia 33(3):190–204
Watanabe T, Watanabe TK, Yamazaki A et al (2019) Coral sclerochronology: similarities and differences in the coral isotopic signatures between mesophotic and shallow-water reefs. In: Loya Y, Puglise KA, Bridge TCL (eds) Mesophotic coral ecosystems. Springer, New York, pp 667–681
Weinstein DK (2014) Deep reef bioerosion and deposition: sedimentology of mesophotic coral reefs in the U.S. Virgin Islands. Dissertation, University of Miami
Weinstein DK, Smith TB, Klaus JS (2014) Mesophotic bioerosion: variability and structural impact on U.S. Virgin Island deep reefs. Geomorphology 222:14–24
Weinstein DK, Klaus JS, Smith TB (2015) Habitat heterogeneity reflected in mesophotic reef sediments. Sediment Geol 329:177–187
Weinstein DK, Sharifi A, Klaus JS et al (2016) Coral growth, bioerosion, and secondary accretion of living orbicellid corals from mesophotic reefs in the US Virgin Islands. Mar Ecol Prog Ser 559:45–63
White KN, Weinstein DK, Ohara T et al (2017) Shifting communities after typhoon damage on an upper mesophotic reef in Okinawa, Japan. PeerJ 5:e3573
Wilkinson CR (1983) Role of sponges in coral reef structural processes. In: Barnes DJ (ed) Perspectives on coral reefs. Australian Institute of Marine Science, Townsville, pp 263–274
Wilson S, Bellwood DR (1997) Cryptic dietary components of territorial damselfishes (Pomacentridae, Labroidei). Mar Ecol Prog Ser 153:299–310
Wisshak M (2012) Microbioerosion. In: Knaust D, Bromley RG (eds) Developments in sedimentology: trace fossils as indicators of sedimentary environments. vol 64. Elsevier, Amsterdam, pp 213–243
Wisshak M, Form A, Jakobsen J et al (2010) Temperate carbonate cycling and water mass properties from intertidal to bathyal depths (Azores). Biogeosciences 7:2379–2396
Wisshak M, Tribollet A, Golubic S et al (2011) Temperate bioerosion: ichnodiversity and biodiversity from intertidal to bathyal depths (Azores). Geobiology 9:492–520
Woods R (1999) Reef evolution. Oxford University Press, Oxford, 426p
Zundelevich A, Lazar B, Ilan M (2007) Chemical versus mechanical bioerosion of coral reefs by boring sponges–lessons from Pione cf. vastifica. J Exp Biol 210:91–96
Acknowledgments
This chapter is dedicated to the memory of Robert Ginsburg, who was an early pioneer advocating mesophotic reef research, as well as a great inspiration, mentor, teacher, and friend. We thank the editors for inviting us to contribute to this important book. Special thanks to Christine Schönberg for providing critical suggestions, edits, and detailed review and to Clark Sherman and William Kiene for reviewing earlier versions of this chapter and suggesting improvements. Alan Weinstein provided editorial review. We also greatly appreciate the constructive comments and suggestions for improving this chapter from Peter Glynn, Chris Perry, Stjepko Golubic, and an anonymous reviewer. USVI funding (to DKW) was provided by the National Science Foundation (NSF), the Geological Society of America, Sigma Xi, ExxonMobil, the Academy of Underwater Arts and Sciences, the RSMAS Graduate Student Fund, the University of Miami Center for Latin American Studies, and the Leonard and Jayne Abess/Citizens Board. Support was also provided by a Zuckerman STEM Postdoctoral Scholarship (DKW). A Sigma Xi Grants-in-Aid of Research (to RLM) and awards from the NSF (BIO-OCE 1635798 and 1800914 to AMSC) also supported this work.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2019 Springer Nature Switzerland AG
About this chapter
Cite this chapter
Weinstein, D.K., Maher, R.L., Correa, A.M.S. (2019). Bioerosion. In: Loya, Y., Puglise, K., Bridge, T. (eds) Mesophotic Coral Ecosystems. Coral Reefs of the World, vol 12. Springer, Cham. https://doi.org/10.1007/978-3-319-92735-0_43
Download citation
DOI: https://doi.org/10.1007/978-3-319-92735-0_43
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-319-92734-3
Online ISBN: 978-3-319-92735-0
eBook Packages: Earth and Environmental ScienceEarth and Environmental Science (R0)