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Russian Journal of Marine Biology

, Volume 44, Issue 3, pp 175–184 | Cite as

An Inventory of Marine Benthic Macroalgae of Hainan Island, China

  • E. A. Titlyanov
  • T. V. Titlyanova
  • X. Li
  • H. Huang
Review
  • 12 Downloads

Abstract

In this review, the results of the study of marine benthic algal flora of Hainan Island, China, during the period from 1933 to 2015 are considered. It has been found that the local floristic diversity and taxonomic composition are similar to those of macroalgae from other large islands of the Indo-Pacific, where coral reefs are the main ecosystem of the shallow-water zone. An analysis of historical (decadal) changes in the marine benthic flora of Hainan has shown the following pattern of variations in the species diversity of macroalgae since the middle of the 20th century: a decline in low-productive epilithic algae with voluminous forms of thalli and an increase in highly productive opportunistic species with filamentous, fine filamentous, and membranous forms. These historical changes are thought to be caused by human impacts: inappropriate exploitation of coral reefs and eutrophication of coastal waters due to household sewage from large cities and discharge of mariculture wastes.

Keywords

inventory macrophytic algae Hainan Island 

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References

  1. 1.
    Guryanova, E.F., Marine zoological expedition to Hainan, Vestn. Akad. Nauk SSSR, 1959, vol. 3, pp. 89–92.Google Scholar
  2. 2.
    Nabivailo, Yu.V. and Titlyanov, E.A., Competitive relationships in natural and artificial algal communities, Russ. J. Mar. Biol., 2006, vol. 32, suppl. 1, pp. S21–S31.CrossRefGoogle Scholar
  3. 3.
    Perestenko, L.P., Vodorosli zaliva Petra Velikogo (Algae of Peter the Great Bay), Leningrad: Nauka, 1980.Google Scholar
  4. 4.
    Sergeeva, O.S., Titlyanova, T.V., and Titlyanov, E.A., Species composition and distribution of algae on the fringing coral reef of Sesoko Island (Ryukyu Archipelago) before and after the natural catastrophe of 1998, Russ. J. Mar. Biol., 2007, vol. 33, no. 1, pp. 30–42.CrossRefGoogle Scholar
  5. 5.
    Titlyanov, E.A. and Titlyanova, T.V., Coral-algal competition on damaged reefs, Russ. J. Mar. Biol., 2008, vol. 34, no. 4, pp. 199–219.CrossRefGoogle Scholar
  6. 6.
    Titlyanov, E.A. and Titlyanova, T.V., Marine plants in a coral reef ecosystem, Russ. J. Mar. Biol., 2012, vol. 38, no. 3, pp. 201–210.CrossRefGoogle Scholar
  7. 7.
    Titlyanov, E.A. and Titlyanova, T.V., Morskie rasteniya Aziatsko-Tikhookeanskogo regiona, ikh ispol’zovanie i kul’tivirovanie (Marie Algae of the Asia-Pacific Region, Their Use and Cultivation), Vladivostok: Dal’nauka, 2012.Google Scholar
  8. 8.
    Titlyanov, E.A. and Titlyanova, T.V., Changes in the species composition of benthic macroalgal communities of the upper subtidal zone on a coral reef in Sanya Bay (Hainan Island, China) during 2009–2012, Russ. J. Mar. Biol., 2013, vol. 39, no. 6, pp. 413–419.CrossRefGoogle Scholar
  9. 9.
    Anthony, K.R.N., Kline, D.I., Diaz-Pulido, G., et al., Ocean acidification causes bleaching and productivity loss in coral reef builders, Proc. Natl. Acad. Sci. U.S.A., 2008, vol. 105, no. 45, pp. 17442–17446.CrossRefPubMedPubMedCentralGoogle Scholar
  10. 10.
    Ateweberhan, M., Bruggemann, J.H., and Breeman, A.M., Effects of extreme seasonality on community structure and functional group dynamics of coral reef algae in the southern Red Sea (Eritrea), Coral Reefs, 2006, vol. 25, pp. 391–406.CrossRefGoogle Scholar
  11. 11.
    Berchez, F.A.S. and Oliveira, E.C., Temporal changes in the benthic marine flora of the Baía de Santos, SP,Brazil, over the last four decades, Algae and Environment: A General Approach, São Paulo: Sociedade Brasileira de Ficologia, 1992, pp. 120–131.Google Scholar
  12. 12.
    Cannicci, S., Gomei, M., Dahdouh-Guebas, F., et al., Influence of seasonal food abundance and quality on the feeding habits of an opportunistic feeder, the intertidal crab Pachygrapsus marmoratus, Mar. Biol., 2007, vol. 151, pp. 1331–1342.CrossRefGoogle Scholar
  13. 13.
    Charpy, L., Charpy-Roubaud, C., and Buat, P., Excess primary production, calcification and nutrient fluxes of a patch reef (Tikehau atoll, French Polynesia), Mar. Ecol.: Prog. Ser., 1998, vol. 173, pp. 139–147.Google Scholar
  14. 14.
    Charpy-Roubaud, C.J. and Charpy, L., Part II: Nutrients, particulate organic matter, and planktonic and benthic production of the Tikehau Atoll (Tuamotu Archipelago French Polynesia), Atoll Res. Bull., 1994, vol. 415, pp. 1–30.CrossRefGoogle Scholar
  15. 15.
    Clements, K.D. and Choat, J.H., Influence of season, ontogeny and tide on the diet of the temperate marine herbivorous fish Odax pullus (Odacidae), Mar. Biol., 1993, vol. 117, pp. 213–220.CrossRefGoogle Scholar
  16. 16.
    Diaz-Pulido, G. and McCook, L., The fate of bleached corals: patterns and dynamics of algal recruitment, Mar. Ecol.: Prog. Ser., 2002, vol. 232, pp. 115–128.Google Scholar
  17. 17.
    Done, T.J., Phase shifts in coral reef communities and their ecological significance, Hydrobiologia, 1992, vol. 247, pp. 121–132.CrossRefGoogle Scholar
  18. 18.
    Fiege, D., Neumann, V., and Li, J., Observations on coral reefs of Hainan Island, South China Sea, Mar. Pollut. Bull., 1994, vol. 29, pp. 84–89.CrossRefGoogle Scholar
  19. 19.
    Fricke, A., Titlyanova, T.V., Nugues, M.M., and Bischof, K., Depth-related variation in epiphytic communities growing on the brown alga Lobophora variegata in a Caribbean coral reef, Coral Reefs, 2011, vol. 30, pp. 967–973.CrossRefGoogle Scholar
  20. 20.
    Furnas, M., Mitchell, A., and Skuza, M., Shelf-scale nitrogen and phosphorus budgets for the central Great Barrier Reef (16–19° S), Proc. 8 Int. Coral Reef Symp., 1997, vol. 1, pp. 809–814.Google Scholar
  21. 21.
    Gartner, A., Lavery, P., and Smit, A.J., Use of δ15N signatures of different functional forms of macroalgae and filter feeders to reveal temporal and spatial patterns in sewage dispersal, Mar. Ecol.: Prog. Ser., 2002, vol. 235, pp. 63–73.Google Scholar
  22. 22.
    Glynn, P.W. and Enochs, I.C., Invertebrates and their roles in coral reef ecosystems, in Coral Reefs: An Ecosystem in Transition, Dordrecht: Springer-Verlag, 2011, pp. 273–326.CrossRefGoogle Scholar
  23. 23.
    Harley, C.D.G., Anderson, K.M., Demes, K.W., et al., Effects of climate change on global seaweed communities, J. Phycol., 2012, vol. 48, pp. 1064–1078.CrossRefPubMedGoogle Scholar
  24. 24.
    Hepburn, C.D., Pritchard, D.W., Cornwall, C.E., et al., Diversity of carbon use strategies in a kelp forest community: Implications for a high CO2 ocean, Global Change Biol., 2011, vol. 17, pp. 2488–2497.CrossRefGoogle Scholar
  25. 25.
    Hoegh-Guldberg, O., Mumby, P.J., Hooten, A.J., et al., Coral reefs under rapid climate change and ocean acidification, Science, 2007, vol. 318, pp. 1737–1742.CrossRefPubMedGoogle Scholar
  26. 26.
    Hughes, R.N. and Seed, R., Behavioural mechanisms of prey selection in crabs, J. Exp. Mar. Biol. Ecol., 1995, vol. 193, pp. 225–238.CrossRefGoogle Scholar
  27. 27.
    Huisman, J.M. and Borowitzka, M.A., Marine benthic flora of the Dampier Archipelago, Western Australia, The Marine Flora and Fauna of Dampier, Western Australia, Perth: West. Aust. Mus., 2003, pp. 291–344.Google Scholar
  28. 28.
    Hutchings, P.A. and Wu, B.L., Coral reefs of Hainan Island, South China Sea, Mar. Pollut. Bull., 1987, vol. 18, pp. 25–26.CrossRefGoogle Scholar
  29. 29.
    Jokiel, P.L., Rodgers, K.S., Kuffner, I.B., et al., Ocean acidification and calcifying reef organisms: A mesocosm investigation, Coral Reefs, 2008, vol. 27, pp. 473–483.CrossRefGoogle Scholar
  30. 30.
    Karez, R., Engelbert, S., Kraufvelin, P., et al., Biomass response and changes in composition of ephemeral macroalgal assemblages along an experimental gradient of nutrient enrichment, Aquat. Bot., 2004, vol. 78, pp. 103–117.CrossRefGoogle Scholar
  31. 31.
    Kennish, R., Williams, G.A., and Lee, S.Y., Algal seasonality on an exposed rocky shore in Hong Kong and the dietary implications for the herbivorous crab Grapsus albolineatus, Mar. Biol., 1996, vol. 125, pp. 55–64.CrossRefGoogle Scholar
  32. 32.
    Kinzie, R.A., Four decades of macroalgal stasis and change on an urban coral reef, Micronesica, 2008, vol. 40, no. 1/2, pp. 101–122.Google Scholar
  33. 33.
    Knowlton, N., Thresholds and multiple stable states in coral reef community dynamics, Am. Zool., 1992, vol. 32, pp. 674–682.CrossRefGoogle Scholar
  34. 34.
    Kuffner, I.B., Andersson, A.J., Jokiel, P.L., et al., Decreased abundance of crustose coralline algae due to ocean acidification, Nat. Geosci., 2008, vol. 1, pp. 114–117.CrossRefGoogle Scholar
  35. 35.
    Lapointe, B.E., Nutrient thresholds for bottom-up control of macroalgal blooms on coral reefs in Jamaica and southeast Florida, Limnol. Oceanogr., 1997, vol. 42, pp. 1119–1131.CrossRefGoogle Scholar
  36. 36.
    Lapointe, B.E., Barile, P.J., Littler, M.M., et al., Macroalgal blooms on southeast Florida coral reefs: I. Nutrient stoichiometry of the invasive green alga Codium isthmocladum in the wider Caribbean indicates nutrient enrichment, Harmful Algae, 2005, vol. 4, pp. 1092–1105.CrossRefGoogle Scholar
  37. 37.
    Lapointe, B.E., Barile, P.J., Littler, M.M., and Littler, D.S., Macroalgal blooms on southeast Florida coral reefs: II. Cross-shelf discrimination of nitrogen sources indicates widespread assimilation of sewage nitrogen, Harmful Algae, 2005, vol. 4, pp. 1106–1122.CrossRefGoogle Scholar
  38. 38.
    Lapointe, B.E., Barile, P.J., Wynne, M.J., and Yentsch, C.S., Reciprocal Caulerpa invasion: Mediterranean native Caulerpa ollivieri in the Bahamas supported by human nitrogen enrichment, Aquat. Invaders, 2005, vol. 16, pp. 1–5.Google Scholar
  39. 39.
    Lapointe, B.E. and Bedford, B.J., Ecology and nutrition of invasive Caulerpa brachypus f. parvifolia blooms on coral reefs off southeast Florida, U.S.A., Harmful Algae, 2010, vol. 9, pp. 1–12.CrossRefGoogle Scholar
  40. 40.
    Lapointe, B.E., Littler, M.M., and Littler, D.S., Macroalgal overgrowth of fringing coral reefs at Discovery Bay, Jamaica: bottom-up versus top-down control, Proc. 8 Int. Coral Reef Symp., 1997, vol. 1, pp. 927–932.Google Scholar
  41. 41.
    Lewis, J.E. and Norris, J.N., A history and annotated account of the benthic marine algae of Taiwan, Smithson. Contrib. Mar. Sci., 1987, no. 29, pp. 1–38.CrossRefGoogle Scholar
  42. 42.
    Li, X.B., Liu, S., Huang, H., et al., Coral bleaching caused by an abnormal water temperature rise at Luhuitou fringing reef, Sanya Bay, China, Aquat. Ecosyst. Health Manage., 2012, vol. 15, no. 2, pp. 227–233.CrossRefGoogle Scholar
  43. 43.
    Lirman, D., Competition between macroalgae and corals: Effects of herbivore exclusion and increased algal biomass on coral survivorship and growth, Coral Reefs, 2001, vol. 19, pp. 392–399.CrossRefGoogle Scholar
  44. 44.
    Lüning, K., Seaweeds: Their Environment, Biogeography, and Ecophysiology, New York: Wiley, 1990.Google Scholar
  45. 45.
    Malta, E.-J. and Verschuure, J.M., Effects of environmental variables on between-year variation of Ulva growth and biomass in a eutrophic brackish lake, J. Sea Res., 1997, vol. 38, pp. 71–84.CrossRefGoogle Scholar
  46. 46.
    McClanahan, T.R., Marnane, M.J., Cinner, J.E., and Kiene, W.E., A comparison of marine protected areas and alternative approaches to coral-reef management, Curr. Biol., 2006, vol. 16, pp. 1408–1413.CrossRefPubMedGoogle Scholar
  47. 47.
    McCook, L.J., Macroalgae, nutrients and phase shifts on coral reefs: Scientific issues and management consequences for the Great Barrier Reef, Coral Reefs, 1999, vol. 18, pp. 357–367.CrossRefGoogle Scholar
  48. 48.
    McCook, L.J., Jompa, J., and Diaz-Pulido, G., Competition between corals and algae on coral reefs: a review of evidence and mechanisms, Coral Reefs, 2001, vol. 19, pp. 400–417.CrossRefGoogle Scholar
  49. 49.
    McManus, J.W. and Polsenberg, J.F., Coral-algal phase shifts on coral reefs: ecological and environmental aspects, Prog. Oceanogr., 2004, vol. 60, pp. 263–279.CrossRefGoogle Scholar
  50. 50.
    Nakano, Y., Global environmental change and coral bleaching, Coral Reefs of Japan, Tokyo: Minist. Environ., 2004, pp. 42–48.Google Scholar
  51. 51.
    Oliveira, E.C. and Qi, Y., Decadal changes in a polluted bay as seen from its seaweed flora: The case of Santos Bay in Brazil, Ambio, 2003, vol. 32, pp. 403–405.CrossRefPubMedGoogle Scholar
  52. 52.
    Petraitis, P.S. and Dudgeon, S.R., Detection of alternative stable states in marine communities, J. Exp. Mar. Biol. Ecol., 2004, vol. 300, pp. 343–371.CrossRefGoogle Scholar
  53. 53.
    Roleda, M.Y., Boyd, P.W., and Hurd, C.L., Before ocean acidification: calcifier chemistry lessons, J. Phycol., 2012, vol. 48, pp. 840–843.CrossRefPubMedGoogle Scholar
  54. 54.
    Sfriso, A. and Curiel, D., Check-list of seaweeds recorded in the last 20 years in Venice lagoon and a comparison with the previous records, Bot. Mar., 2007, vol. 50, pp. 2–58.CrossRefGoogle Scholar
  55. 55.
    Silva, P.C., Geographic patterns of diversity in benthic marine algae, Pac. Sci., 1992, vol. 46, pp. 429–437.Google Scholar
  56. 56.
    Silva, P.C., Menez, E.G., and Moe, R.L., Catalog of the benthic marine algae of the Philippines, Smithson. Contrib. Mar. Sci., 1987, vol. 27, pp. 1–179.CrossRefGoogle Scholar
  57. 57.
    Tadashi, K., Dai, C.F., Park, H.-S., et al., Status of coral reefs in East and North Asia (China, Hong Kong, Taiwan, South Korea and Japan), Status of Coral Reefs of the World, Townsville, Australia: Global Coral Reef Monit. Network, 2008, pp. 145–158.Google Scholar
  58. 58.
    Titlyanov, E.A., Titlyanova, T.V., and Chapman, D., Dynamics and patterns of algal colonization of mechanically damaged and dead colonies of the coral Porites lutea, Bot. Mar., 2008, vol. 51, pp. 285–296.CrossRefGoogle Scholar
  59. 59.
    Titlyanov, E.A., Kiyashko, S.I., Titlyanova, T.V., et al., Nitrogen sources to macroalgal growth in Sanya Bay (Hainan Island, China), Curr. Dev. Oceanogr., 2011, vol. 2, pp. 65–84.Google Scholar
  60. 60.
    Titlyanov, E.A., Titlyanova, T.V., Xia, B.M., and Bartsch, I., Checklist of marine benthic green algae (Chlorophyta) on Hainan, a subtropical island off the coast of China: Comparisons between the 1930s and 1990–2009 reveal environmental changes, Bot. Mar., 2011, vol. 54, pp. 523–535.Google Scholar
  61. 61.
    Titlyanov, E.A., Titlyanova, T.V., Huang, H., and Li, X., Seasonal changes in benthic algal communities of the upper subtidal zone in Sanya Bay (Hainan Island, China), J. Mar. Biol. Assoc. U. K., 2014, vol. 94, no. 1, pp. 51–64.CrossRefGoogle Scholar
  62. 62.
    Titlyanov, E.A., Titlyanova, T.V., Li, X., et al., Seasonal changes in the intertidal algal communities of Sanya Bay (Hainan Island, China), J. Mar. Biol. Assoc. U. K., 2014, vol. 94, no. 5, pp. 879–893.CrossRefGoogle Scholar
  63. 63.
    Titlyanov, E.A., Titlyanova, T.V., Belous, O.S., and Kalita, T.L., Inventory change 1990s–2010s in the marine flora of Sanya Bay (Hainan Island, China), J. Mar. Biol. Assoc. U. K., 2015, vol. 95, no. 3, pp. 461–470.CrossRefGoogle Scholar
  64. 64.
    Titlyanov, E.A., Titlyanova, T.V., Li, X., et al., Recent 2008–2012 seaweed flora of Hainan Island, South China Sea, Mar. Biol. Res., 2015, vol. 11, no. 5, pp. 540–550.CrossRefGoogle Scholar
  65. 65.
    Titlyanov, E.A., Titlyanova, T.V., Xia, B.M., and Bartsch, I., Retrospective analysis of diversity and species composition of marine macroalgae of Hainan Island (China), Ocean Sci. J., 2016, vol. 51, no. 3, pp. 485–506.CrossRefGoogle Scholar
  66. 66.
    Titlyanova, T.V., Titlyanov, E.A., Xia, B., and Bartsch, I., New records of benthic marine green algae (Chlorophyta) for the island of Hainan, China, Nova Hedwigia, 2012, vol. 94, nos. 3–4, pp. 441–470.CrossRefGoogle Scholar
  67. 67.
    Titlyanova, T.V., Titlyanov, E.A., and Kalita, T.L., Marine algal flora of Hainan Island: a comprehensive synthesis, Coastal Ecosyst., 2014, vol. 1, pp. 28–53.Google Scholar
  68. 68.
    Tseng, C.K., Studies on the marine Chlorophyceae from Hainan. I, Chin. Mar. Biol. Bull., 1936, vol. 1, pp. 129–200.Google Scholar
  69. 69.
    Tseng, C.K., Common Seaweeds of China, Beijing: Science Press, 1983.Google Scholar
  70. 70.
    Tseng, C.K., The past, present and future of phycology in China, Hydrobiologia, 2004, vol. 512, pp. 11–20.CrossRefGoogle Scholar
  71. 71.
    Tsuda, R.T., Checklist and bibliography of the marine benthic algae from the Mariana Islands (Guam and CNMI), Univ. Guam Mar. Lab., Tech. Rep., 2003, vol. 107, pp. 1–49.Google Scholar
  72. 72.
    Tsuda, R.T., Checklist and bibliography of the marine benthic algae within Chuuk, Pohnpei, and Kosrae States, Federated States of Micronesia, Bishop Mus., Tech. Rep., 2006, no. 34, pp. 1–35.Google Scholar
  73. 73.
    Zhang, S., The species distribution of the seaweeds in the coast of China seas, Chin. Biodiversity, 1996, vol. 4, pp. 139–144.Google Scholar
  74. 74.
    Zhang, G., Que, H., Liu, X., and Xu, H., Abalone mariculture in China, J. Shellfish Res., 2004, vol. 23, pp. 947–950.Google Scholar
  75. 75.
    Zhang, Q., Shi, Q., Chen, G., et al., Status monitoring and health assessment of Luhuitou fringing reef of Sanya, Hainan, China, Chin. Sci. Bull., 2006, vol. 51, pp. 81–88.CrossRefGoogle Scholar
  76. 76.
    Zhang, Q., Xu, X.Z., and Long, X.M., A numerical study on internal tides in the northeast of the South China Sea, Trop. Oceanol., 1996, vol. 14, pp. 15–23.Google Scholar

Copyright information

© Pleiades Publishing, Ltd. 2018

Authors and Affiliations

  • E. A. Titlyanov
    • 1
  • T. V. Titlyanova
    • 1
  • X. Li
    • 2
  • H. Huang
    • 2
  1. 1.Zhirmunsky Institute of Marine Biology, National Scientific Center of Marine Biology, Far Eastern BranchRussian Academy of SciencesVladivostokRussia
  2. 2.Tropical Marine Biological Research Station in HainanChinese Academy of SciencesSanyaChina

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