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Differential response of coral communities to Caulerpa spp. bloom in the reefs of Indian Ocean

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Abstract

Coral reef ecosystems are disturbed in tandem by climatic and anthropogenic stressors. A number of factors act synergistically to reduce the live coral cover and threaten the existence of reefs. Continuous monitoring of the coral communities during 2012–2014 captured an unprecedented growth of macroalgae as a bloom at Gulf of Mannar (GoM) and Palk Bay (PB) which are protected and unprotected reefs, respectively. The two reefs varying in their protection level enabled to conduct an assessment on the response of coral communities and their recovery potential during and after the macroalgal bloom. Surveys in 2012 revealed a live coral cover of 36.8 and 14.6% in GoM and PB, respectively. Live coral cover was lost at an annual rate of 4% in PB due to the Caulerpa racemosa blooms that occurred in 2013 and 2014. In GoM, the loss of live coral cover was estimated to be 16.5% due to C. taxifolia bloom in 2013. Tissue regeneration by the foliose and branching coral morphotypes aided the recovery of live coral cover in GoM, whereas the chances for the recovery of live coral cover in PB reef were low, primarily due to frequent algal blooms, and the existing live coral cover was mainly due to the abundance of slow-growing massive corals. In combination, results of this study suggested that the recovery of a coral reef after a macroalgal bloom largely depends on coral species composition and the frequency of stress events. A further study linking macroalgal bloom to its specific cause is essential for the successful intervention and management.

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References

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

    Article  CAS  Google Scholar 

  • Bender D, Diaz-Pulido G, Dove S (2012) Effects of macroalgae on corals recovering from disturbance. J of Exp Mar Biol and Ecol 429:15–19

    Article  Google Scholar 

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

    Article  CAS  Google Scholar 

  • Bonaldo RM, Hay ME (2014) Seaweed-coral interactions: variance in seaweed allelopathy, coral susceptibility, and potential effects on coral resilience. PLoS One 9:e85786

    Article  Google Scholar 

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

    Article  Google Scholar 

  • Burke L, Selig E, Spalding M (2006) Reefs at risk in Southeast Asia. World Resources Institute, Washington, DC

    Google Scholar 

  • Diaz-Pulido G, McCook LJ (2005) Effects of nutrient enhancement on the fecundity of a coral reef macroalga. J Exp Mar Biol Ecol 317:13–24

    Article  Google Scholar 

  • Diaz-Pulido G, McCook LJ (2008) Environmental status: macroalgae (seaweeds). In: Chin A (ed) The state of the great barrier reef . Great Barrier Reef Marine Park Authority, Townsville, AustraliaOnline

    Google Scholar 

  • Diaz-Pulido G, McCook LJ, Dove S, Berkelmans R, Roff G, Kline DI, Weeks S, Evans RD, Williamson DH, Hoegh-Guldberg O (2009) Doom and boom on a resilient reef: climate change, algal overgrowth and coral recovery. PLoS One 4:e5239

    Article  Google Scholar 

  • Edmunds PJ, Carpenter RC (2001) Recovery of Diadema antillarum reduces macroalgal cover and increases abundance of juvenile corals on a Caribbean reef. Proc Natl Acad Sci 98:5067–5071

    Article  CAS  Google Scholar 

  • Edward JKP, Mathews G, Patterson J, Wilhelmsson D (2007) Coral reef of the Gulf of Mannar, southeastern India-distribution, diversity and status. Sugandhi Devadasan Marine Research Institute, Tuticorin, p. 120

    Google Scholar 

  • English S, Wilkinson C, Baker V (1997) Survey manual for tropical marine resources 2nd ed. Australian Institute of Marine Science. Townsville, Australia

    Google Scholar 

  • Fung T, Seymour RM, Johnson CR (2011) Alternative stable states and phase shifts in coral reefs under anthropogenic stress. Ecology 92:967–982

    Article  Google Scholar 

  • Gates RD, Baghdasarian G, Muscatine L (1992) Temperature stress causes host cell detachment in symbiotic cnidarians: implications for coral bleaching. Biol Bull 182:324–332

    Article  Google Scholar 

  • Gilmour JP, Smith LD, Heyward AJ, Baird AH, Pratchett MS (2013) Recovery of an isolated coral reef system following severe disturbance. Science 340:69–71

    Article  CAS  Google Scholar 

  • Harley CDG, Anderson KM, Demes KW, Jorve JP, Kordas RL, Coyle TA (2012) Effects of climate change on global seaweed communities. J Phycol 48:1064–1078

    Article  CAS  Google Scholar 

  • Hughes T, Szmant AM, Steneck R, Carpenter R, Miller S (1999) Algal blooms on coral reefs: what are the causes? Limnol Oceanogr 44:1583–1586

    Article  CAS  Google Scholar 

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

    Article  Google Scholar 

  • Hunter CL, Evans CW (1994) Reefs in Kaneohe Bay, Hawaii: two centuries of western influence and two decades of data. In: Ginzburg RM (ed) Proceedings of the colloquium on global aspects of coral reefs: health, hazards and history. University of Miami, Florida, pp. 339–345

    Google Scholar 

  • Idjadi JA, Lee SC, Bruno JF, Precht WF, Allen-Requa L, Edmunds PJ (2006) Rapid phase-shift reversal on a Jamaican coral reef. Coral Reefs 25:209–211

    Article  Google Scholar 

  • Jasmine S (2013) Mass spawning of Scleractinian corals in the Lakshadweep Archipelago. http://eprints.cmfri.org.in/9365/1/147.pdf (accessed on 30 May 2015)

  • Johnson CR, Mann KH (1986) The crustose coralline alga, Phymatolithon Foslie, inhibits the overgrowth of seaweeds without relying on herbivores. J Exp Mar Biol and Ecol 96:127–146

    Article  Google Scholar 

  • Jompa J, McCook LJ (2003) Coral-algal competition: macroalgae with different properties have different effects on corals. Mar Ecol Prog Ser 258:87–95

    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 

  • Manikandan B, Ravindran J, Shrinivaasu S, Marimuthu N, Paramasivam K (2014) Community structure and coral status across reef fishing intensity gradients in Palkbay, southeast coast of India. Env Monit and Ass 186:5989–6002

    Article  CAS  Google Scholar 

  • Martin-Smith KM (1993) The phenology of four species of Sargassum at magnetic island, Australia. Bot Mar 36:327–334

    Article  Google Scholar 

  • McClanahan TR (1995) A coral reef ecosystem-fisheries model: impacts of fishing intensity and catch selection on reef structure and processes. Ecol Model 80:1–19

    Article  CAS  Google Scholar 

  • McCook L, 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 

  • McCook LJ (1999) Macroalgae, nutrients and phase shifts on coral reefs: scientific issues and management consequences for the great barrier reef. Coral Reefs 18(4):357–367

    Article  Google Scholar 

  • Miller IR (2003) Crown-of-thorns starfish and coral surveys using the manta tow and scuba search technicques. Standard operational procedure No. 8. SOP 8. Australian Institute of Marine Science, pp. 43, http://epubs.aims.gov.au/handle/110687/7487

  • NIO report (2012) Environmental impact assessment of the 4A alignment of the Sethusamudram ship can project. Ministry of Shipping, New Delhi

    Google Scholar 

  • Norström AV, Lokrantz J, Nystrom M, Yap HT (2007) Influence of dead coral substrate morphology on patterns of juvenile coral distribution. Mar Biol 150:1145–1152

    Article  Google Scholar 

  • Norström AV, Nyström M, Lokrantz J, Folke C (2009) Alternative states on coral reefs: beyond coral-macroalgal phase shifts. Mar Ecol Prog Ser 376:295–306

    Article  Google Scholar 

  • Nugues MM, Delvoye L, Bak RPM (2004) Coral defence against macroalgae: differential effects of mesenterial filaments on the green alga Halimeda opuntia. Mar Ecol Prog Ser 278:103–114

    Article  Google Scholar 

  • Nystrom M, Folke C (2001) Spatial resilience of coral reefs. Ecosystems 4(5):406–417

    Article  Google Scholar 

  • Paine RT (1980) Food webs: linkage, interaction strength and community infrastructure. J Anim Ecol 89:667–685

    Google Scholar 

  • Raj KD, Patterson J (2010) Observations on the reproduction of Acropora corals along the Tuticorin coast of the Gulf of Mannar, southeastern India. Ind J Mar Sci 39:219–226

    Google Scholar 

  • Rasher DB, Stout EP, Engel MS, Kubanek J, Hay ME (2011) Macroalgal terpenes function as allelopathic agents against reef corals. Proc Natl Acad of Sci 108:17726–17731

    Article  CAS  Google Scholar 

  • Ravindran J, Kannapiran E, Manikandan B, ManiMurali R, Joseph A (2012) Bleaching and secondary threats on the corals of Palk Bay: a survey and proactive conservation needs. Ind J of Geo Mar Sci 41:19–26

    Google Scholar 

  • Shinn EA (1976) Coral reef recovery in Florida and the Persian Gulf. Env Geol 1:241–254

    Article  Google Scholar 

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

    Article  Google Scholar 

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

  • Szmant AM (2002) Nutrient enrichment on coral reefs: is it a major cause of coral reef decline? Estuaries 25(4):743–766

    Article  CAS  Google Scholar 

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

    Article  Google Scholar 

  • Venkataraman K, Rajkumar R (2013) Status of coral reefs in Palk Bay. Records of Zoological Survey India 113:1–11

    Google Scholar 

  • Venkataraman K, Satyanarayana CH, Alfred JRB, Wolstenholme J (2003) Handbook on hard corals of India. Zoological Survey of India, Kolakatta

    Google Scholar 

  • Vermeij MJA, Dailer ML, Smith CM (2011) Crustose coralline algae can suppress macroalgal growth and recruitment on Hawaiian coral reefs. Mar Ecol Prog Ser 422:1–7

    Article  Google Scholar 

  • Veron JEN (2000) Corals of the world. In: Stafford-Smith M (ed) Australian Institute of Marine Science. Townsville, Australia

    Google Scholar 

  • Vuki VC, Price IR (1998) Seasonal changes in the Sargassum populations on a fringing coral reef, magnetic island, great barrier reef region, Australia. Aquat Bot 48:153–166

    Article  Google Scholar 

  • Wallace CC, Watt A, Bull GD (1986) Recruitment of juvenile corals onto coral tables preyed upon by Acanthaster planci. Mar Ecol Prog Ser 32:299–306

    Article  Google Scholar 

Download references

Acknowledgements

The authors thank the Dr. S.W.A. Naqvi, Director, CSIR- National Institute of Oceanography for his encouragement and support. The first author thanks the Department of Science and Technology, Government of India, for the award of INSPIRE fellowship (Grant No. IF110663) and Mr. Kathiresan, Boat Personnel, for his logistical support and assistance during field activities. NIO contribution number: 5963.

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  1. Biological Oceanography Division, CSIR - National Institute of Oceanography, Dona Paula, Panaji, Goa -, 403004, India

    B. Manikandan & J. Ravindran

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  1. B. Manikandan
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  2. J. Ravindran
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Correspondence to J. Ravindran.

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Manikandan, B., Ravindran, J. Differential response of coral communities to Caulerpa spp. bloom in the reefs of Indian Ocean. Environ Sci Pollut Res 24, 3912–3922 (2017). https://doi.org/10.1007/s11356-016-8136-5

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