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Phototactic responses in the gametes of the brown alga, Ectocarpus siliculosus

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Abstract

The action spectrum of phototaxis was determined and the photoreceptive mechanism was studied in Ectocarpus gametes (Ectocarpales, Phaeophyceae) using a computerized cell-tracking system. The fine structures of the stigma and the flagellar swelling were analyzed, and the reflective function of the stigma was demonstrated for the first time. Under monochromatic light stimulation, Ectocarpus gametes show mainly positive phototaxis between 370 nm and 520 nm. The action spectrum has a minor peak near 380 nm, and two major peaks at 430 nm and 450 nm or 460 nm and a shoulder at 470 nm adjoining a remarkable depression near 440 nm. Under unilateral stroboscopic illumination with more than four pulses per second, the gametes show clear phototaxis. However, the response is disturbed at lower frequencies. Addition of methyl cellulose, which increases the viscosity of the medium and slows down gamete rotation, decreases the threshold frequency. These results indicate that rotation of the gamete plays an essential role in the photoreceptive mechanism. Under equal intensities of bilateral illumination at an angle of 90°, most of the gametes swim on the resultant between the two light beams. This response is disturbed when the angle of the two light beams is as large as 120°. Observations by transmission electron microscopy show that the flagellar swelling fits precisely into a concave depression of the chloroplast at the central region of the stigma. Electron-dense material is present in that sector of the flagellar swelling which faces away from the stigma. Epifluorescence microscopy without a barrier filter and epipolarization microscopy reveal that stigmata reflect blue light. A hypothesis is formulated which discusses the possibility that the reflected light is focused onto the flagellar swelling.

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References

  • Buder, J. (1919) Zur Kenntnis der phototaktischen Richtungsbewegungen. Jahrb. Wiss. Bot. 58, 105–220

    Google Scholar 

  • Coleman, A.W. (1988) The autofluorescent flagellum: a new phylogenetic enigma. J. Phycol. 24, 118–120

    Google Scholar 

  • Diehn, B. (1973) Phototaxis in Euglena. 1.: Physiological basis of photoreceptor and tactic orientation, In: Behaviour of Micro-organisms, pp. 83–90, Perez-Miravete, A., ed. Plenum Press, London

    Google Scholar 

  • Dodge, J.D. (1975) The fine structure of algal cells. Academic Press, London

    Google Scholar 

  • Foster, K.W., Smyth, R.D. (1980) Light antennas in phototactic algae. Microbiol. Rev. 44, 572–630

    Google Scholar 

  • Geller, A., Müller, D.G. (1981) Analysis of the flagellar beat pattern of male Ectocarpus siliculosus gametes (Phaeophyta) in relation to chemotactic stimulation by female cells. J. Exp. Biol. 92, 53–66

    Google Scholar 

  • Häder, D.-P. (1987) Polarotaxis, gravitaxis and vertical phototaxis in the green flagellate, Euglena gracilis. Arch. Microbiol. 147, 179–183

    Google Scholar 

  • Häder, D.-P., Lebert, M. (1985) Real time computer-controlled tracking of motile microorganisms. Photochem. Photobiol. 42, 509–524

    Google Scholar 

  • Häder, D.-P., Lebert, M., Di Lena, M.R. (1986) New evidence for the mechanism of phototactic orientation of Euglena gracilis. Curr. Microbiol. 14, 157–163

    Google Scholar 

  • Kawai, H. (1988) A flavin-like autofluorescent substance in the posterior flagellum of golden and brown algae. J. Phycol. 24, 114–117

    Google Scholar 

  • Kawai, H., Inouye, I. (1989) Flagellar autofluorescence in forty-four chlorophyll c-containing algae. Phycologia 28, 222–227

    Google Scholar 

  • Kawai, H., Kubota, M., Kondo, T., Watanabe, M. (1990) Action spectra of the phototaxis in zoospore of a brown alga Pseudochorda sp. Protoplasma, in press

  • Moestrup, O. (1982) Flagellar structure in algae: a review, with new observations particularly on the Chrysophyceae, Phaeophyceae (Fucophyceae), Euglenophyceae, and Reckertia. Phycologia 21, 427–528

    Google Scholar 

  • Müller, D.G. (1979) Genetic affinity of Ectocarpus siliculosus (Dillw.) Lyngb. from the Mediterranean, North Atlantic and Australia. Phycologia 18, 312–318

    Google Scholar 

  • Müller, D.G., Maier, I., Müller, H. (1987) Flagellum autofluorescence and photoaccumulation in heterokont algae. Photochem. Photobiol. 46, 1003–1008

    Google Scholar 

  • Starr, R.C. (1978) The culture collection of algae at the University of Texas at Austin. J. Phycol. 14 (Suppl.), 47–100

    Google Scholar 

  • Spurr, A.R. (1969) A low-viscosity epoxy resin-embedding medium for electron microscopy. J. Ultrastruct. Res. 26, 31–43

    Google Scholar 

  • Walne, P.L., Arnott, H.J. (1967) The comparative ultrastructure and possible function of stigmata: Euglena granulata and Chlamydomonas eugametos. Planta 77, 325–353

    Google Scholar 

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We are grateful to Jochen Schäfer and Elke Reinecke for their technical assistance and Dr. G. Konerman for access to epipolarization microscopy. We are also grateful to the Alexander von Humboldt Foundation for a Research Fellowship to H.K. and the Deutsche Forschungsgemeinschaft (University of Freiburg, Freiburg, FRG) for financial aid to D.-P.H.

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Kawai, H., Müller, D.G., Fölster, E. et al. Phototactic responses in the gametes of the brown alga, Ectocarpus siliculosus . Planta 182, 292–297 (1990). https://doi.org/10.1007/BF00197124

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  • DOI: https://doi.org/10.1007/BF00197124

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