Low electric current density enhances the calcification rate of the colonial Stony Coral Galaxea fascicularis

References

• Allemand, D., Christine Ferrier-Pagès, Furla, P., Fanny Houlbrèque, Puverel, S., & Stéphanie R., et al. 2004. Biomineralisation in reef-building corals: from molecular mechanisms to environmental control. CR Palevol 3, 453–467.
   Web of Science ®Google Scholar
• Anthony, K.R.N., Willis, B.L., 2002. Comparative analysis of energy allocation to tissue and skeletal growth in corals. Limnol. Oceanogr. 47, 1417–1429. doi:10.4319/lo.2002.47.5.1417
   Web of Science ®Google Scholar
• Badger, M.R., Price, G.D., 1994. The role of carbonic anhydrase in photosynthesis. Plant Biol. 45, 369–392. doi:10.1146/annurev.pp.45.060194.002101
   Web of Science ®Google Scholar
• Barott, K. L., Perez, S. O., Linsmayer, L. B., & Tresguerres, M., 2015. Differential localization of ion transporters suggests distinct cellular mechanisms for calcification and photosynthesis between two coral species. Am. J. Physiol. Regul. Integr. Comp. Physiol. 309, R235–R246. doi:10.1152/ajpregu.00052.2015
   PubMed Web of Science ®Google Scholar
• Barron, M.E., Thies, A.B., Espinoza, J.A., Barott, K.L., Hamdoun, A., Tresguerres, M., 2018. A vesicular Na+/Ca2+ exchanger in coral calcifying cells. PLOS One, 13. doi:10.1371/journal.pone.0205367
   Web of Science ®Google Scholar
• Beer, S., Vilenkin, B., Weil, A., Veste, M., Susel, L., Eshel, A., 1998. Measuring photosynthetic rates in seagrasses by pulse amplitude modulated (PAM) fluorometry. Mar. Ecol. Prog. Ser. 174, 293–300. doi:10.3354/meps174293
   Web of Science ®Google Scholar
• Borell, E.M., Romatzki, S.B.C., Ferse, S.C.A., 2010. Differential physiological responses of two congeneric scleractinian corals to mineral accretion and an electric field. Coral Reefs 29, 191–200. doi:10.1007/s00338-009-0564-y
   Web of Science ®Google Scholar
• Comeau, S., Tambutté, E., Carpenter, R. C., Edmunds, P. J., Evensen, N. R., & Allemand, D., et al. 2017. Coral calcifying fluid pH is modulated by seawater carbonate chemistry not solely seawater pH. Proc. Royal Soc. B 284.
   Google Scholar
• Damayanti, L.P.A., Ahyadi, H., Candri, D.A., Sabil, A., 2011. Growth rate of Acropora formosa and Montipora digitata transplanted on biorock in Gili Trawangan. Journal of Indonesian. Coral Reefs 1, 114–119
   Google Scholar
• Dickson, A.G., Sabine, C.L., Christian, J.R. (Eds.), 2007. Guide to Best Practices for Ocean CO₂ Measurements. PICES Special Publication. North Pacific Marine Science Organization, Sidney, British Columbia. 191 pp.
   Google Scholar
• Eashwar, M., Sathish Kumar, P., Ravishankar, R., & Subramanian, G., 2013. Sunlight-enhanced calcareous deposition on cathodic stainless steel in natural seawater. Biofouling 29, 185–193. doi:10.1080/08927014.2012.755673
   PubMed Web of Science ®Google Scholar
• Erez, J., Braun, A., 2007. Calcification in hermatypic corals is based on direct seawater supply to the biomineralization site. Geochimica et Cosmochimica Acta 71, A260–A260.
   Web of Science ®Google Scholar
• Estes, A.M., Kempf, S.C., Henry, R.P., 2003. Localization and quantification of carbonic anhydrase activity in the symbiotic scyphozoan Cassiopea xamachana. Biol. Bull. 204, 278–289. doi:10.2307/1543599
   PubMed Web of Science ®Google Scholar
• Feng, Y., Hare, C. E., Rose, J. M., Handy, S. M., Ditullio, G. R., & Lee, P. A., et al. 2010. Interactive effects of iron, irradiance and CO2 on Ross Sea phytoplankton. Deep-Sea Res. Part I 57, 368–383.
   Google Scholar
• Ferrario, F., Beck, M.W., Storlazzi, C.D., Micheli, F., Shepard, C.C., Airoldi, L., 2014. The effectiveness of coral reefs for coastal hazard risk reduction and adaptation. Nat. Commun. 5, 3794. doi:10.1038/ncomms4794
   PubMed Web of Science ®Google Scholar
• Gorbatsevich, L.I., 1997. Initial survival of coral nubbins transplanted by a new coral transplantation technology-options for reef rehabilitation. Mar. Ecol. Prog. Ser. 150, 287–292.
   Web of Science ®Google Scholar
• Goreau, T.J., 2012. Innovative methods of marine ecosystem restoration. CRC Press 5, 205–230.
   Google Scholar
• Goreau, T.J., 2014. Electrical stimulation greatly increases settlement, growth, survival, and stress resistance of marine organisms. Nat. Resour. Forum 05, 527–537. doi:10.4236/nr.2014.510048
   Google Scholar
• Hilbertz, W.H., 1992. Solar-generated building material from seawater as a sink for carbon. AMBIO 21, 126–129.
   Web of Science ®Google Scholar
• Hilbertz, W.H., Goreau, T.J., 1996. Method of enhancing the growth of aquatic organisms, and structures created thereby: US. Patent number 5 US Patent Office, pp14.
   Google Scholar
• Hoegh-Guldberg, O., 1988. A method for determining the surface area of corals. Coral Reefs 7, 113–116. doi:10.1007/BF00300970
   Web of Science ®Google Scholar
• Huang, B., Yuan, X., Huang, H., Liu, S., 2017. Comparison of calcium carbonate crystals and coral bone crystals by electrodeposition of seawater. Ocean Sci. 41(07), 113–119.
   Google Scholar
• Jokiel, P.L., Maragos, J.E., Franzisket, L., 1978. Coral growth: buoyant weight technique. In: Stoddart, D.R., Johannes, R.E. (Eds.), Coral Reefs: Research Methods, pp. 529–542. UNESCO Monographs on Oceanographic Methodology, Paris.
   Google Scholar
• Jones, R.J., 1997. Zooxanthellae loss as a bioassay for assessing stress in corals. Mar. Ecol. Prog. Ser. 149, 163–171. doi:10.3354/meps149163
   Web of Science ®Google Scholar
• Jones, R.J., Yellowlees, D., 1997. Regulation and control of intracellular algae (= zooxanthellae) in hard corals. Philos. Trans. Royal Soc. B 352, 457–468. doi:10.1098/rstb.1997.0033
   Web of Science ®Google Scholar
• Kihara, K., Taniguchi, H., Koibuchi, Y., Yamamoto, S., Kondo, Y., Hosokawa, Y., 2013. Enhancing settlement and growth of corals using feeble electrochemical method. Galaxea, JCRS 15, 323–329. doi:10.3755/galaxea.15.323
   Google Scholar
• Levas, S. J., Andréa G. Grottoli, Hughes, A., Osburn, C. L., & Matsui, Y., 2013. Physiological and biogeochemical traits of bleaching and recovery in the mounding species of coral Porites lobata: Implications for resilience in mouding corals. PLOS One, 8. doi:10.1371/journal.pone.0063267
   PubMed Web of Science ®Google Scholar
• Lin, D., Smith, M.A., Elter, J., Champagne, C., Downey, C.L., Beck, J., Offenbacher, S., 2003. The mechanism of calcification and its relation to photosynthesis and respiration in the scleractinian coral Galaxea fascicularis. Mar. Biol. 142, 419–426.
   Web of Science ®Google Scholar
• Moya, A., Tambutté, S., Tambutté, E., Zoccola, D., Caminiti, N., Allemand, D., 2006. Study of calcification during a daily cycle of the coral Stylophora pistillata: implications for light-enhanced calcification. J. Exp. Biol. 209, 3413–3419. doi:10.1242/jeb.02382
   PubMed Web of Science ®Google Scholar
• Olivotto, I., Planas, M., Simões, N, Holt, G., Avella, M., & Calado, R., 2011. Advances in breeding and rearing marine ornamentals. J. World Aquacult. Soc. 42, 135–166. doi:10.1111/j.1749-7345.2011.00453.x
   Web of Science ®Google Scholar
• Osinga, R., Redeker, D., Beukelaar, P.B., Wijffels, R.H., 1999. Measurement of sponge growth by projected body area and underwater weight. Optik 125, 3756–3758.
   Google Scholar
• Ralph, P.J., Gademann, R., 2005. Rapid light curves: A powerful tool to assess photosynthetic activity. Aquat. Bot. 82, 222–237. doi:10.1016/j.aquabot.2005.02.006
   Web of Science ®Google Scholar
• Rinkevich, B., 2005. Conservation of coral reefs through active restoration measures: Recent approaches and last decade progress. Environ. Sci. Technol. 39, 4333–4342. doi:10.1021/es0482583
   PubMed Web of Science ®Google Scholar
• Rollion-Bard, C., Blamart, D., 2015. Possible controls on Li, Na, and Mg incorporation into aragonite coral skeletons. Chem. Geol. 396, 98–111. doi:10.1016/j.chemgeo.2014.12.011
   Web of Science ®Google Scholar
• Romatzki, S.B.C., 2014. Influence of electrical fields on the performance of Acropora coral transplants on two different designs of structures. Mar. Biol. Res. 10, 449–459. doi:10.1080/17451000.2013.814794
   Web of Science ®Google Scholar
• Sabater, M.G., Yap, H.T., 2002. Growth and survival of coral transplants with and without electrochemical deposition of CaCO3. J. Exp. Mar. Biol. Ecol. 272, 131–146. doi:10.1016/S0022-0981(02)00051-5
   Web of Science ®Google Scholar
• Sabater, M.G., Yap, H.T., 2004. Long-term effects of induced mineral accretion on growth, survival and corallite properties of Porites cylindrica Dana. J. Exp. Mar. Biol. Ecol. 311, 355–374. doi:10.1016/j.jembe.2004.05.013
   Web of Science ®Google Scholar
• Schreiber, U., 2004. Pulse-Amplitude-Modulation (PAM) fluorometry and saturation pulse method: An overview. In: Papageorgiou, G.C., Govindjee (Eds.), Chlorophyll a Fluorescence. Advances in Photosynthesis and Respiration, Springer Netherlands. 19, 279–319.
   Google Scholar
• Schuhmacher, H., Schillak, L., 1994. Integrated electrochemical and biogenic deposition of hard material—a nature-like colonization substrate. B. Mar. Sci. 55, 672–679.
   Web of Science ®Google Scholar
• Schutter, M., Crocker, J., Paijmans, A., Janse, M., Osinga, R., Verreth, A.J., Wijffels, R.H., 2010. The effect of different flow regimes on the growth and metabolic rates of the scleractinian coral Galaxea fascicularis. Coral Reefs 29, 737–748. doi:10.1007/s00338-010-0617-2
   Web of Science ®Google Scholar
• Schutter, M., Kranenbarg, S., Wijffels, R.H., Verreth, J., Osinga, R., 2011. Modification of light utilization for skeletal growth by water flow in the scleractinian coral Galaxea fascicularis. Mar. Biol. 158, 769–777. doi:10.1007/s00227-010-1605-3
   Web of Science ®Google Scholar
• Senatore, A., Raiss, H., Le, P., 2016. Physiology and evolution of voltage-gated calcium channels in early diverging animal phyla: Cnidaria, Placozoa, Porifera and Ctenophora. Front. Physiol. 7. doi:10.3389/fphys.2016.00481
   PubMed Web of Science ®Google Scholar
• Spencer Davies, P., 1989. Short-term growth measurements of corals using an accurate buoyant weighing technique. Mar. Biol. 101(3), 389–395. doi:10.1007/BF00428135
   Web of Science ®Google Scholar
• Stromberg, S.M., Lundalv, T., Goreau, T.J., 2010. Suitability of mineral accretion as a rehabilitation method for cold-water coral reefs. J. Exp. Mar. Biol. Ecol. 395, 153–161. doi:10.1016/j.jembe.2010.08.028
   Web of Science ®Google Scholar
• Tambutté S, Holcomb M, Ferrier-Pagès C, Reynaud S, Tambutté É, Zoccola D, Allemand D., 2011. Coral biomineralization: From the gene to the environment. J. Exp. Mar. Biol. Ecol. 408, 58–78. doi:10.1016/j.jembe.2011.07.026
   Web of Science ®Google Scholar
• Wells, S., Samoilys, M., Makoloweka, S., Kalombo, H., 2010. Lessons learnt from a collaborative management program in coastal Tanzania. Ocean Coast. Manage. 53(4), 161–168. doi:10.1016/j.ocecoaman.2010.01.007
   Web of Science ®Google Scholar
• Wilbur, K.M., Watabe, N., 1976. The mechanisms of mineralization in the invertebrates and plants: symposium. Published for the Belle W. Baruch Institute for Marine Biology and Coastal Research by the University of South Carolina Press, Columbia. 196, 1704–1709.
   Google Scholar
• Wright, J.C., Holliday, C.W., Odonnell, M.J., 1994. Na+/K+-ATPase activity in the pleopods and hindgut-rectum of terrestrial isopods - implications for colligative water-vapor absorption. J. Crustac. Biol. 14, 522–529. doi:10.2307/1548998
   Web of Science ®Google Scholar
• Zheng, X., Guo, F., Liu, X., Lin, R., Zhou, Z., Shi, X., 2015. Ocean acidification did not significantly affect the calcification and photosynthesis of adult staghorn cup coral. J. Oceanology, 37(10), 59–68.
   Google Scholar
• Zheng, X., Li, Y., Chen, S., Lin, R., 2018. Effects of calcium ion concentration on calcification rates of six stony corals: A mesocosm study. Aquaculture 497, 246–252. doi:10.1016/j.aquaculture.2018.07.041
   Web of Science ®Google Scholar