全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Longitudinal Observation of Japanese Lancelet, Branchiostoma japonicum, Metamorphosis

DOI: 10.7167/2013/839671

Full-Text   Cite this paper   Add to My Lib

Abstract:

The lancelet (amphioxus) performs metamorphosis and produces minute and ciliate pelagic larvae commonly found in other metamorphic marine invertebrates. During larval life and metamorphosis, however, the animal displays interesting combination of features not found in other animals such as long coexistence of ciliate and muscular locomotion and no change in feeding behavior. The uniqueness of lancelet metamorphosis can provide important data to understand the evolutionary history of this animal as well as the metamorphosis broadly appeared in metazoans. Although lancelet metamorphosis has been studied, all previous studies depended on cross-sectional observations. To get serial data on metamorphic events, we performed longitudinal observations on the Japanese lancelet under the culture condition and confirmed the following: (1) there were individual variations of the duration of metamorphosis from 15 to 27 days; (2) growth was arrested for a month and the maximum reduction of the body length (2.2%–3.2%) occurred when gill slits became paired; (3) during rather long duration of metamorphosis, the oral transformation and the division of the gill pores by tongue bar were completed within two to four days. Our observations suggest that the duration and mode of lancelet metamorphosis depend mainly on intrinsic requirements rather than on extrinsic selective pressures. 1. Introduction Profound change of body plan under the same genomic background during life cycle is common in metazoans. It is called metamorphosis and found in at least some species of most extant phyla [1]. Metamorphosis of lancelets (amphioxus) has been noticed from the first embryological study of Kowalevsky [2] and interested the following scientists such as Lankester and Willey [3], Willey [4], and van Wijhe [5]. Like other marine invertebrates, lancelets change their life mode from pelagic to benthic passing through metamorphosis. However, their diet and feeding method are not changed principally. Lancelet ontogeny uniquely displays a long-term coexistence of cilia- and muscle-driving locomotion before metamorphosis [6, 7]. The metamorphosis takes place after pelagic larval life, the duration of which depends on the environmental condition and species [8–10], and animals after metamorphosis settle into sand substratum. Metamorphic changes mainly occur in the pharyngeal region in lancelets. Metapleural folds appear first on the ventral trunk on both sides and fused ventrally covering the original body surface in the pharyngeal region and abdominal region anterior to the iliocolonic ring

References

[1]  S. M. Degnan and B. M. Degnan, “The initiation of metamorphosis as an ancient polyphenic trait and its role in metazoan life-cycle evolution,” Philosophical Transactions of the Royal Society B, vol. 365, no. 1540, pp. 641–651, 2010.
[2]  A. Kowalevsky, “Entwickelingsgeschichte des Amphioxus lancelolatus,” L'Académie Impériale des Sciences de St. Pétersburg, vol. 11, no. 4, pp. 1–17, 1867.
[3]  E. R. Lankester and A. Willey, “The development of the atrial chamber of amphioxus,” Quarterly Journal of Microscopic Science, vol. 31, no. 123, pp. 445–466, 1890.
[4]  A. Willey, “The later larval development of amphioxus,” Quarterly Journal of Microscopic Science, vol. 32, no. 126, pp. 183–234, 1891.
[5]  J. W. van Wijhe, “On the metamorphosis of Amphioxus lanceolatus,” Konikijke Akademie van Wetenschappen te Amsterdam, vol. 16, pp. 574–583, 1914.
[6]  F. S. Chia, J. Buckland-Nicks, and C. M. Young, “Locomotion of marine invertebrate larvae: a review,” Canadian Journal of Zoology, vol. 62, no. 7, pp. 1205–1222, 1984.
[7]  M. D. Stokes, “Larval locomotion of the lancelet Branchiostoma floridae,” Journal of Experimental Biology, vol. 200, no. 11, pp. 1661–1680, 1997.
[8]  J. E. Webb, “The ecology of Lagos Lagoon. III. The life history of Branchiostoma nigeriense Webb,” Transactions of the Royal Society B, vol. 241, no. 683, pp. 335–353, 1958.
[9]  J. H. Wickstead, “Chordata: acrania (Cephalochordata),” in Reproduction of Marine Invertebrates, A. C. Giese and J. S. Pearse, Eds., vol. 2 of Entoprocts and Lesser Coelomates, pp. 282–319, Academic Press, New York, NY, USA, 1975.
[10]  M. D. Stokes and N. D. Holland, “Embryos and larvae of a lancelet, Branchiostoma floridae, from hatching through metamorphosis: growth in the laboratory and external morphology,” Acta Zoologica, vol. 76, no. 2, pp. 105–120, 1995.
[11]  M. Urata, N. Yamaguchi, Y. Henmi, and K. Yasui, “Larval development of the oriental lancelet, Branchiostoma belcheri, in laboratory mass culture,” Zoological Science, vol. 24, no. 8, pp. 787–797, 2007.
[12]  G. Williams, Adaptation and Natural Selection, Princeton University Press, Princeton, NJ, USA, 1966.
[13]  L. Z. Holland, et al., “The amphioxus genome illuminates vertebrate origins and cephalochordate biology,” Genome Research, vol. 18, no. 7, pp. 1100–1111, 2008.
[14]  M. G. Hadfield, “Why and how marine-invertebrate larvae metamorphose so fast,” Seminars in Cell and Developmental Biology, vol. 11, no. 6, pp. 437–443, 2000.
[15]  M. Paris, H. Escriva, M. Schubert et al., “Amphioxus postembryonic development reveals the homology of chordate metamorphosis,” Current Biology, vol. 18, no. 11, pp. 825–830, 2008.
[16]  Q. J. Zhang, J. Zhong, S. H. Fang, and Y. Q. Wang, “Branchiostoma japonicum and B. belcheri are distinct lancelets (Cephalochordata) in Xiamen waters in China,” Zoological Science, vol. 23, no. 6, pp. 573–579, 2006.
[17]  K. Yasui, M. Urata, N. Yamaguchi, H. Ueda, and Y. Henmi, “Laboratory culture of the oriental lancelet Branchiostoma belcheri,” Zoological Science, vol. 24, no. 5, pp. 514–520, 2007.
[18]  M. D. Stokes and N. D. Holland, “Ciliary hovering in larval lancelets (= amphioxus),” Biological Bulletin, vol. 188, no. 3, pp. 231–233, 1995.
[19]  J. H. Wickstead and Q. Bone, “Ecology of acraniate larvae,” Nature, vol. 184, no. 4702, pp. 1849–1851, 1959.
[20]  J. E. Webb, “On the feeding and behaviour of the larva of Branchiostoma lanceolatum,” Marine Biology, vol. 3, no. 1, pp. 58–72, 1969.
[21]  P. T. Walsh, J. R. Downie, and P. Monaghan, “Plasticity of the duration of metamorphosis in the African clawed toad,” Journal of Zoology, vol. 274, no. 2, pp. 143–149, 2008.
[22]  A. Willey, Amphioxus and the Ancestor of the Vertebrates, Macmillan, London, UK, 1894.
[23]  J. H. Wickstead, “Branchiostoma lanceolatum larvae: some experiments on the effect of thiouracil on metamorphosis,” Journal of the Marine Biological Association, vol. 47, no. 1, pp. 49–59, 1967.
[24]  E. J. W. Barrington, “The digestive system of Amphioxus (Branchiostoma) lanceolatum,” Philosophical Transactions of the Royal Society B, vol. 228, pp. 269–312, 1937.
[25]  H. Ueda and K. Sakaki, “Effects of turbation of the Japanese common lancelet Branchiostoma japonicum (Cephalochordata) on sediment condition: laboratory observation,” Plankton and Benthos Research, vol. 2, no. 3, pp. 155–160, 2007.
[26]  D. G. Shu, H. L. Luo, S. Conway Morris et al., “Lower Cambrian vertebrates from south China,” Nature, vol. 402, no. 6757, pp. 42–46, 1999.
[27]  N. H. Putnam, T. Butts, D. E. K. Ferrier et al., “The amphioxus genome and the evolution of the chordate karyotype,” Nature, vol. 453, no. 7198, pp. 1064–1071, 2008.
[28]  T. Kon, M. Nohara, Y. Yamanoue, Y. Fujiwara, M. Nishida, and T. Nishikawa, “Phylogenetic position of a whale-fall lancelet (Cephalochordata) inferred from whole mitochondrial genome sequences,” BMC Evolutionary Biology, vol. 7, article 127, 2007.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133