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Marine Biology

, Volume 144, Issue 4, pp 665–674 | Cite as

Ultrastructure of post-fertilization development in the red alga Callophyllis linearis (Kallymeniaceae, Cryptonemiales, Rhodophyta)

  • S. G. DelivopoulosEmail author
Research Article

Abstract

The ultrastructure of post-fertilization development of the red alga Callophyllis linearis (Kyl.) Abb. & Norr. of the Kallymeniaceae showed that the Kallymeniaceae are more closely related to the Cryptomeniales than to the Gigartinales. The auxiliary cell produces multinucleate gonimoblast initials which divide to produce generative gonimoblast cells. These cells undergo repeated cleavages to form clusters of carpospore initials, which finally differentiate into carpospores. Carpospore differentiation is simple and occurs in three developmental stages. In the first stage, young carpospores are avacuolate, contain a large nucleus, have few undeveloped plastids and exhibit incipient dictyosome activity. During the intermediate stage, plastids develop their internal thylakoid system, starch granules are formed and dictyosomes continue to produce vesicles that contribute carpospore wall material. The formation of fibrous vacuoles originates from the fibrous vacuole associated organelles (FVAOs). In the final stage, mature carpospores form cored vesicles. They also contain well-developed plastids, fibrous vacuoles, numerous starch granules and are surrounded by a two-layered carpospore wall.

Keywords

Starch Granule Auxiliary Cell Carpogonial Branch Floridean Starch Thylakoid Formation 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Notes

Acknowledgements

I gratefully acknowledge Dr. Ursula Luetz-Meindl for her critical review and constructive suggestions for improving the manuscript.

References

  1. Abbott IA, Hollenberg GI (1976) Marine algae of California. Stanford University Press, StanfordGoogle Scholar
  2. Bold HW, Wynne MJ (1985) Introduction to the algae—structure and reproduction, 2nd edn. Prentice-Hall, Englewood Cliffs, N.J.Google Scholar
  3. Broadwater S, Scott J (1982) Ultrastructure of early development in the female reproductive system of Polysiphonia harveyi Bailey (Ceramiales, Rhodophyta). J Phycol 18:427–441Google Scholar
  4. Broadwater S, Scott J (1983) Fibrous vacuole associated organelles (FVAOs) in the Florideophyceae: a new interpretation of the “appareil cinétique”. Phycologia 22:225–233Google Scholar
  5. Chamberlain AH, Evans LV (1973) Aspects of spore production in the red alga Ceramium. Protoplasma 76:139–159Google Scholar
  6. Delivopoulos SG (2000) Ultrastructure of spermatiogenesis in the red alga Osmundea spectabilis var. spectabilis (Rhodomelaceae, Ceramiales, Rhodophyta). Phycologia 39:517–526Google Scholar
  7. Delivopoulos SG (2002) Ultrastructure of tetrasporogenesis in the red alga Osmundea spectabilis var. spectabilis (Rhodomelaceae: Ceramiales: Rhodophyta). Mar Biol 140:921–934CrossRefGoogle Scholar
  8. Delivopoulos SG (2003) Ultrastructure of post-fertilization development in the red alga Nienburgia andersoniana (Delesseriaceae, Ceramiales, Rhodophyta). Bot J Linn Soc 142:289–299Google Scholar
  9. Delivopoulos S, Diannelidis BE (1991a) Ultrastructure of carposporophyte development in the red alga Ceramium strictum (Rhodophyta, Ceramiales). Microbios 65:71–80Google Scholar
  10. Delivopoulos S, Diannelidis BE (1991b) Ultrastructure of carpospore differentiation in the red alga Ceramium strictum Greville and Harvey (Ceramiales, Ceramiaceae). Ann Sci Nat Bot 13(II):9–21Google Scholar
  11. Delivopoulos S, Diannelidis BE (1991c) Ultrastructure of carpospore differentiation in the red alga Alsidium corallinum C. Agardh. (Ceramiales, Rhodomelaceae). Ann Sci Nat Bot 13(II):23–31Google Scholar
  12. Delivopoulos S, Kugrens P (1984) Ultrastructure of carposporogenesis in the parasitic red alga Faucheocolax attenuata Setch. (Rhodymeniales, Rhodymeniaceae). Am J Bot 71:1245–1259Google Scholar
  13. Delivopoulos S, Kugrens P (1985) Ultrastructure of carposporophyte development in the red alga Gloiosiphonia verticillaris (Cryptonemiales, Gloiosiphoniaceae). Am J Bot 72:1926–1938Google Scholar
  14. Delivopoulos SG, Polne-Fuller M, Diannelidis BE (1999) Ultrastructural study of the differentiated blade of Porphyra perforata (Rhodophyta). Nova Hedwigia 68:65–74Google Scholar
  15. Gori P (1980) Ultrastructure of carpospores in Gastroclonium clavatum Ardissone (Rhodymeniales). Protoplasma 103:263–271Google Scholar
  16. Hommersand MH, Ott DW (1970) Development of the carposporophyte of Kallymenia reniformis (Turner) J. Agardh. J Phycol 6:322–331Google Scholar
  17. Konrad-Hawkins E (1974) Golgi vesicles of uncommon morphology and wall formation in the red alga, Polysiphonia. Protoplasma 80:1–14PubMedGoogle Scholar
  18. Kugrens P (1974) Light and electron microscope studies of the development and liberation of Janczewskia gardneri Setch spermatia (Rhodophyta). Phycologia 13:295–306Google Scholar
  19. Kugrens P (1980) Electron microscopic observations on the differentiation and release of spermatia in the marine red alga Polysiphonia hendryi (Ceramiales, Rhodomelaceae). Am J Bot 67:519–528Google Scholar
  20. Kugrens P, Delivopoulos SG (1986) Ultrastructure of the carposporophyte and carposporogenesis in the parasitic red alga Plocamiocolax pulvinata Setch. (Gigartinales, Plocamiaceae). J Phycol 22:8-21Google Scholar
  21. Kugrens P, West JA (1973) The ultrastructure of carpospore differentiation in the parasitic red alga Levringiella gardneri (Setch) Kylin. Phycologia 12:163–173Google Scholar
  22. Kugrens P, West JA (1974) The ultrastructure of carposporogenesis in the marine hemiparasitic red alga Erythrocystis saccata. J Phycol 10:139–147Google Scholar
  23. Kylin H (1928) Entwicklungsgeschichtliche Florideen-studien. Acta Univ Lund 24(4):1–127Google Scholar
  24. Kylin H (1930) Über die Entwicklungsgeschichte der Florideen. Acta Univ Lund 26(6):1–104Google Scholar
  25. Kylin H (1932) Die Florideenordnung Gigartinales. Acta Univ Lund 28(8):1–88Google Scholar
  26. Kylin H (1956) Die Gattungen der Rhodophyceen. CWK Gleerups, LundGoogle Scholar
  27. Pueschel CM (1992) An ultrastructural survey of the diversity of crystalline proteinaceous inclusions in red algal cells. Phycologia 31:489–499Google Scholar
  28. Ramm-Anderson SM, Wetherbee R (1982) Structure and development of the carposporophyte of Nemalion helminthoides (Nemalionales, Rhodophyta). J Phycol 1:133–141Google Scholar
  29. Triemer RE, Vasconcelos AC (1977) The ultrastructure of carposporogenesis in Caloglossa leprieurii (Delesseriaceae, Ceramiales). Am J Bot 64:825–834Google Scholar
  30. Tripodi G (1971) The fine structure of the cystocarp in the red alga Polysiphonia sertularioides (Grat.) J. Ag. J Submicr Cytol 3:71–79Google Scholar
  31. Tripodi G (1974) Ultrastructural changes during carpospore formation in the red alga Polysiphonia. J Submicr Cytol 6:275–286Google Scholar
  32. Tripodi G, Gargiulo GM (1984) Relationships among membranes in plastids of the red alga Nitophyllum punctatum (Stackh) Grev. Protoplasma 119:55–61Google Scholar
  33. Tsekos I (1982) Plastid development and floridean starch grain formation during carposporogenesis in the red alga Gigartina teedii. Cryptog Algol 3:91–103Google Scholar
  34. Tsekos I, Schnepf E (1983) The ultrastructure of carposporogenesis in Gigartina teedii (Roth) Lamour. (Gigartinales, Rhodophyceae): auxiliary cell, cystocarpic plant. Flora 173:81–96Google Scholar
  35. Wetherbee R (1978) Differentiation and continuity of the Golgi apparatus during carposporogenesis in Polysiphonia (Rhodophyta). Protoplasma 95:347–360Google Scholar
  36. Wetherbee R (1980) Postfertilization development in the red alga Polysiphonia 1. Proliferation of the carposporophyte. J Ultrastruct Res 70:259–274PubMedGoogle Scholar
  37. Wetherbee R, West JA (1977) Golgi apparatus of unique morphology during early carposporogenesis in a red alga. J Ultrastruct Res 58:119–133Google Scholar
  38. Wetherbee R, Wynne MJ (1973) The fine structure of the nucleus and nuclear association of developing carposporangia in Polysiphonia novae-angliae (Rhodophyta). J Phycol 9:402–407Google Scholar
  39. Wetherbee R, Janda DM, Bretherton GA (1984) The structure, composition and distribution of proteinaceous crystalloids in vegetative cells of the red alga Wrangelia plumosa. Protoplasma 119:135–140Google Scholar

Copyright information

© Springer-Verlag 2003

Authors and Affiliations

  1. 1.Department of BotanyAristotle University of ThessalonikiThessalonikiGreece

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