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Rhythmic contractions of the ampullar epidermis during metamorphosis of the ascidian Molgula occidentalis

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Summary

The ampullae of Molgula occidentalis are hollow, tubular extensions of the epidermis. They are ensheathed by a secreted tunic. When they grow out shortly after settlement, the ampullae spread the tunic over the substratum to form a firm attachment for the sessile juvenile. A simple squamous epithelium forms the thin ampullar walls. A glandular, simple columnar epithelium forms the distal tip of each ampulla. The glandular cells probably secrete the adhesive that attaches the tunic to the substratum.

Repetitive, peristaltic contractions pass from the base to the distal end of each ampulla. Microsurgery, time-lapse cinemicrography and TEM have been used to analyze this phenomenon. The contractions are mediated by a layer of 4–8 nm microfilaments in the base of the ampullar epithelium.

Each juvenile has 7–9 ampullae which contract at different frequencies. Isolated ampullae continue to contract normally for several days. Thus each ampulla has an intrinsic rhythm. Microsurgical experiments suggest that there is no specific region within an ampulla with unique pacemaker properties. It is proposed that communication via gap junctions allows the coordination of ampullar cells into a well organized peristaltic wave.

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References

  • Abbott DP (1953) Asexual reproduction in the colonial ascidian Metandrocarpa taylori Huntsman. U Calif Publ Zool 61:1–78

    Google Scholar 

  • Abbott DP (1955) Larval structure and activity in the ascidian Metandrocarpa taylori. J Morphol 97:569–594

    Google Scholar 

  • Bancroft FW (1899) A new function of the vascular ampullae in the Botryllidae. Zool Anz 22:450–462

    Google Scholar 

  • Berrill NJ (1929) Studies in tunicate development. Part I. General physiology of development of simple ascidians. Phil Trans Roy Soc 218B:37–78

    Google Scholar 

  • Berrill NJ (1931) Studies in tunicate development II. Abbreviation of development in the Molgulidae. Phil Trans Roy Soc 219B:281–346

    Google Scholar 

  • Berrill NJ (1949) The gonads, larvae and budding of the polystyelid ascidians Stolonica and Distomus. J Mar Biol Ass UK 28:633–650

    Google Scholar 

  • Berrill NJ (1950) The Tunicata with an account of the British species. Ray Society, London

    Google Scholar 

  • Bone Q, Mackie GO (1975) Skin impulses and locomotion in Oikopleura (Tunicata: Larvacea). Biol Bull 149:267–286

    Google Scholar 

  • Brewin BI (1959) An account of larval budding in the compound ascidian Hypsistozoa fasmeriana. Quart J Microsc Sci 100:575–589

    Google Scholar 

  • Carlisle DB (1961) Locomotory powers of adult ascidians. Proc Zool Soc London 136:141–146

    Google Scholar 

  • Cloney RA (1966) Cytoplasmic filaments and cell movements: Epidermal cells during ascidian metamorphosis. J Ultrastr Res 14:300–328

    Google Scholar 

  • Cloney RA (1969) Cytoplasmic filaments and morphogenesis: The role of the notochord in ascidian metamorphosis. Z Zellforsch 100:31–53

    Google Scholar 

  • Cloney RA (1972) Cytoplasmic filaments and morphogenesis: Effects of Cytochalasin-B on contractile epidermal cells. Z Zellforsch 132:167–192

    Google Scholar 

  • Cloney RA (1978) Ascidian metamorphosis: Review and analysis. In: Chia F-S, Rice M (eds) Settlement and metamorphosis in marine invertebrate larvae. Elsevier-New York, New York Oxford, pp 255–282

    Google Scholar 

  • Cloney RA, Florey E (1968) Ultrastructure of cephalopod chromatophre organs. Z Zellforsch 89: 250–280

    Google Scholar 

  • Deck JD, Hay ED, Revel J-P (1966) Fine structure and origin of the tunic of Perophora viridis. J Morphol 120:267–280

    Google Scholar 

  • DeLeo G, Patricolo E, D'Ancona Lunetta G (1977) Studies on the fibrous components of the test of Ciona intestinalis L. I. Cellulose-like polysaccharide. Acta Zool (Stockh) 58:135–141

    Google Scholar 

  • DeSanto RS, Dudley PL (1969) Ultramicroscopic filaments in the ascidian Botryllus schlosseri (Pallas) and their possible role in ampullar contractions. J Ultrastr Res 28:259–274

    Google Scholar 

  • Dilly PN (1969) The ultrastructure of the test of the tadpole larva of Ciona intestinalis. Z Zellforsch 95:331–346

    Google Scholar 

  • Endean R (1955) Studies of the blood and tests of some Australian ascidians. III. The formation of the test of Pyura stolonifera (Heller). Austr J Mar Freshw Res 6:157–164

    Google Scholar 

  • Endean R (1961) The test of the ascidian Phallusia mammillata. Quart J Microsc Sci 102:107–117

    Google Scholar 

  • Faulkner GT (1970) Formation and fine structure of the larval tunic in simple ascidians. PhD thesis, U of Wisconsin

  • Georges D (1979) Gap and tight junctions in tunicates. Study in conventional and freeze-fracture techniques. Tiss & Cell 11:781–792

    Google Scholar 

  • Grave C (1926) Molgula citrina (Alder and Hancock). Activities and structure of the free-swimming larva. J Morphol 42:453–467

    Google Scholar 

  • Katow H, Watanabe H (1978) Fine structure and possible role of ampullae on tunic supply and attachment in a compound ascidian, Botryllus primigenus Oka. J Ultrastr Res 64:23–34

    Google Scholar 

  • Korn ED (1978) Biochemistry of actomyosin-dependent cell motility (A review). Proc Natl Acad Sci USA 75:588–599

    Google Scholar 

  • Lash JW, Cloney RA, Minor RR (1973) The effect of Cytochalasin-B upon tail resorption and metamorphosis in ten species of ascidians. Biol Bull 145:360–372

    Google Scholar 

  • Luft JH (1961) Improvements in epoxy resin embedding methods. J Biophys Biochem Cytol 9:409–414

    Article  CAS  PubMed  Google Scholar 

  • Mackie GO, Bone Q (1976) Skin impulses and locomotion in an ascidian tadpole. J Mar Biol Ass UK 56:751–768

    Google Scholar 

  • Mackie GO, Bone Q (1977) Locomotion and propagated skin impulses in salps (Tunicata: Thaliacea). Biol Bull 153:180–197

    Google Scholar 

  • Millar RH (1951) The stolonic vessels of the Didemnidae. Quart J Microsc Sci 92:249–254

    Google Scholar 

  • Mukai H, Sugimoto K, Taneda Y (1978) Comparative studies on the circulatory system of the compound ascidians Botryllus, Botrylloides and Symplegma. J Morphol 157:49–77

    Google Scholar 

  • Newberry AT (1965a) Vascular structures associated with budding in the polystyelid ascidian Metandrocarpa taylori. Ann Soc Roy Zool Belg 95:57–74

    Google Scholar 

  • Newberry AT (1965b) The structure of the circulatory apparatus of the test and its role in budding in the polystyelid ascidian Metandrocarpa taylori Huntsman. Mem Acad Roy Belg, Cl Sci sect 2 16:1–57

    Google Scholar 

  • Scott FM (1952) The developmental history of Amaroucium constellatum. III. Metamorphosis. Biol Bull 103:226–241

    Google Scholar 

  • Sebastian VO (1953) The development of Herdmania pallida (Heller). Proc Ind Acad Sci 37:174–187

    Google Scholar 

  • Smith MJ (1970) The blood cells and tunic of the ascidian Halocynthia aurantium (Pallas). II. Histochemistry of the blood cells and tunic. Biol Bull 138:379–388

    Google Scholar 

  • Staehelin LA (1974) Structure and function of intercellular junctions. Intern Rev Cytol 39:191–284

    Google Scholar 

  • Terakado K (1970) Tunic formation in the larva of the ascidian Perophora orientalis. Sci Rep Saitama Univ (B) 5:183–191

    Google Scholar 

  • Trason WB (1957) Larval structure and development of the oozooid in the ascidian Euherdmania claviformis. J Morphol 100:509–546

    Google Scholar 

  • Wardrop AB (1970) The structure and formation of the test of Pyura stolonifera. Protoplasma 70:73–86

    Google Scholar 

  • Willey A (1900) On the protostigmata of Molgula manhattensis (DeKay). Quart J Microsc Sci 44:141–159

    Google Scholar 

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Torrence, S.A., Cloney, R.A. Rhythmic contractions of the ampullar epidermis during metamorphosis of the ascidian Molgula occidentalis . Cell Tissue Res. 216, 293–312 (1981). https://doi.org/10.1007/BF00233621

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