Citation: | Xia Guangyuan, Wang Dexiang. Observation on the morphology and wound-healing process of Tethya sp.[J]. Haiyang Xuebao, 2017, 39(4): 89-100. doi: 10.3969/j.issn.0253-4193.2017.04.0099 |
Sponges of Porifera have powerful regeneration capacity. Among them, the genus Tethya is a special group, which has differentiation in cortex and choanoderm. In this paper, the morphology of Tethya sp., and its wound-healing process were studied by removing specific part of some tissues, to understand the transformation of Tethya sp. and the role of different tissues in the healing process. The results showed that the main transformation in the wound-healing process is the cell rearrangement resulted by the cell migration from the unwounded to the wounded part, the cortex and choanoderm are vital to the survival of Tethya; while the spicule center is less importance in the wound-healing process.
刘凌云, 郑光美. 普通动物学[M]. 北京: 高等教育出版社, 2009. Liu Lingyun, Zheng Guangmei. General Zoology[M]. Beijing: Higher Education Press, 2009.
|
Duckworth A R. Effect of wound size on the growth and regeneration of two temperate subtidal sponges[J]. Journal of Experimental Marine Biology and Ecology, 2003, 287(2): 139-153.
|
Duckworth A. Farming sponges to supply bioactive metabolites and bath sponges: a review[J]. Marine Biotechnology, 2009, 11(6): 669-679.
|
Morrow C, Cárdenas P. Proposal for a revised classification of the Demospongiae (Porifera)[J]. Frontiers in Zoology, 2015, 12: 7.
|
Gaino E, Liaci L S, Sciscioli M, et al. Investigation of the budding process in Tethya citrina and Tethya aurantium(Porifera, Demospongiae)[J]. Zoomorphology, 2006, 125(2): 87-97.
|
Cardone F, Gaino E, Corriero G. The budding process in Tethya citrina Sarà & Melone (Porifera, Demospongiae) and the incidence of post-buds in sponge population maintenance[J]. Journal of Experimental Marine Biology and Ecology, 2010, 389(1/2): 93-100.
|
Corriero G, Sarà M, Vaccaro P. Sexual and asexual reproduction in two species of Tethya(Porifera: Demospongiae) from a Mediterranean coastal lagoon[J]. Marine Biology, 1996, 126(2): 175-181.
|
Nickel M, Donath T, Schweikert M, et al. Functional morphology of Tethya species (Porifera): 1. Quantitative 3D-analysis of Tethya wilhelma by synchrotron radiation based X-ray microtomography[J]. Zoomorphology, 2006, 125(4): 209-223.
|
Nickel M, Bullinger E, Beckmann F. Functional morphology of Tethya species (Porifera): 2. Three-dimensional morphometrics on spicules and skeleton superstructures of T. minuta[J]. Zoomorphology, 2006, 125(4): 225-239.
|
Nickel M. Like a‘rolling stone’: quantitative analysis of the body movement and skeletal dynamics of the sponge Tethya wilhelma[J]. Journal of Experimental Biology, 2006, 209(15): 2839-2846.
|
Fishelson L. Observations on the moving colonies of the genus Tethya(Demospongia, Porifera)[J]. Zoomorphology, 1981, 98(1): 89-99.
|
Nickel M. Kinetics and rhythm of body contractions in the sponge Tethya wilhelma(Porifera: Demospongiae)[J]. Journal of Experimental Biology, 2004, 207(26): 4515-4524.
|
Ellwanger K, Eich A, Nickel M. GABA and glutamate specifically induce contractions in the sponge Tethya wilhelma[J]. Journal of Comparative Physiology A, 2007, 193(1): 1-11.
|
Ellwanger K, Nickel M. Neuroactive substances specifically modulate rhythmic body contractions in the nerveless metazoon Tethya wilhelma(Demospongiae, Porifera)[J]. Frontiers in Zoology, 2006, 3: 7.
|
Nimeth K T, Egger B, Rieger R, et al. Regeneration in Macrostomum lignano(Platyhelminthes): cellular dynamics in the neoblast stem cell system[J]. Cell and Tissue Research, 2007, 327(3): 637-646.
|
Bond C. Continuous cell movements rearrange anatomical structures in intact sponges[J]. Journal of Experimental Zoology, 1992, 263(3): 284-302.
|