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Asexual reproduction of Pliocene solitary scleractinian coral Truncatoflabellum: a morphological and biometric study

Published online by Cambridge University Press:  20 May 2016

Yuki Tokuda
Affiliation:
Tottori Prefectural Museum, 2-124, Higashi-machi, Tottori 680-0011, Japan,
Yoichi Ezaki
Affiliation:
Department of Geosciences, Osaka City University, Sugimoto, Sumiyoshi-ku, Osaka 558-8585, Japan

Abstract

Truncatoflabellum has been considered a free-living genus that exhibits both sexual and asexual phases; divided lower coralla (anthocauli) are specialized for asexual reproduction by transverse division through a decalcification process, whereas the upper coralla (anthocyathi) only undertake sexual reproduction, in a life-cycle strategy that includes a distinct alternation of generations. However, little evidence has been presented to support this idea of its life cycle. We elucidate the life mode of Truncatoflabellum by identifying key fossil characters (e.g., multiple rejuvenations and decalcification records just beneath lateral spines) and statistically analyzing the size distributions of over 500 individual coralla. Results of those morphological and biometric analyses clearly indicate alternation of generations in the life cycle of Truncatoflabellum.

Type
Research Article
Copyright
Copyright © The Paleontological Society 

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References

Cairns, S. D. 1984. New records of ahermatypic corals (Scleractinia) from the Hawaiian and Line Islands. Occasional Papers Bishop Museum, 25:130.Google Scholar
Cairns, S. D. 1989a. A revision of the ahermatypic Scleractinia of the Philippine Islands and adjacent waters, Part1. Fungiacyathidae, Micrabaciidae, Guyniidae, and Flabellidae. Smithsonian Contributions to Zoology, 486:1136.Google Scholar
Cairns, S. D. 1989b. Asexual reproduction in solitary Scleractinia. Proceedings of the 6th International Coral Reef Symposium, Australia, 2:641646.Google Scholar
Cairns, S. D. 1994. Scleractinia of the temperate North Pacific. Smithsonian Contributions to Zoology, 557:1150.Google Scholar
Cairns, S. D. 1995. The marine fauna of New Zealand: Scleractinia (Cnidaria: Anthozoa). New Zealand Oceanographic Institute Memoir, 103:1210.Google Scholar
Cairns, S. D. 1999. Cnidaria Anthozoa: Deep-water azooxanthellate Scleractinia from Vanuatu, and Wallis and Futuna Islands. Memoires du Museum National d'Histoire Naturelle, 180:31167.Google Scholar
Cairns, S. D., Hoeksema, B. W., and van der Land, J. 1999. List of extant stony corals. Atoll Research Bulletin, 459:1346.Google Scholar
Hoeksema, B. W. 1989. Taxonomy, phylogeny and biogeography of mushroom corals (Scleractinia: Fungiidae). Zoologische Verhandelingen Leiden, 254:1295.Google Scholar
Iwai, M., Kondo, Y., Kikuchi, N., and Oda, M. 2006. Overview of stratigraphy and paleontology of Pliocene Tonohama Group, Kochi Prefecture, southwest Japan. Journal of Geological Society Japan, 112 (Supplement):2740.Google Scholar
Kita, S., Ikehara, M., Kondo, Y., and Iwai, M. 2009. Late Pliocene paleoenvironmental changes from the Ananai Formation drilled core: Evidence for stable isotope ratio. Abstracts of Japan Geoscience Union Meeting 2009, L135-001.Google Scholar
Oliver, W. A. Jr., 1968. Some aspects of colony development in corals. Journal of Paleontology, 42:1634.Google Scholar
Squire, D. F. 1963. Flabellum rubrum (Quoy and Gaimard). New Zealand Oceanographic Institute Memoir, 20:143.Google Scholar
Stolarski, J. 1992. Transverse division in a Miocene scleractinian coral. Acta Palaeontologica Polonica, 36:413426.Google Scholar
Tokuda, Y., Ikeno, T., Goto, S. G., Numata, H., and Ezaki, Y. 2010. Influence of habitat change on the evolution of morphology and life history traits of azooxanthellate solitary corals (Scleractinia: Flabellidae). Biological Journal of the Linnean Society, 101:184192.Google Scholar
Yamashiro, H. and Yamazato, K. 1987. Studies on the detachment of the mushroom coral Fungia fungites with special reference to hard structural changes. Galaxea, 6:163175.Google Scholar
Wells, J. W. 1956. Scleractinia, p. F328T444. InMoore, R. C. (ed.), Treatise on Invertebrate Paleontology. Pt. F. Coelenterata. Geological Society of America and University of Kansas Press, Lawrence, Kansas.Google Scholar
Wells, J. W. 1966. Evolutionary development in the scleractinian family Fungiidae, p. 223246. InRees, W. J. (ed.), The Cnidaria and their evolution. Symposia of the Zoological Society of London, 16.Google Scholar
Wells, J. W. 1984. Notes on Indo-Pacific scleractinian corals. Part 10. Late Pleistocene ahermatypic corals from Vanuatu. Pacific Science, 38:205219.Google Scholar
Yabe, H. and Eguchi, M. 1942a. Fossil and Recent Flabellum from Japan. Scientific Reports of the Tohoku Imperial University, series 2 (Geology), 22:87103.Google Scholar
Yabe, H. and Eguchi, M. 1942b. Fossil and Recent simple corals from Japan. Scientific Reports of the Thohoku Imperial University, series 2 (Geology), 22:105178.Google Scholar
Zibrowius, H. 1985. Asexual reproduction by bud-shedding in shallow-water Balanophylla of the tropical Indo-Pacific (Cnidaria: Scleractinia: Dendrophylliidae). Proceedings of the Fifth International Coral Reef Congress, Tahiti, 5:233238.Google Scholar