Hostname: page-component-586b7cd67f-2plfb Total loading time: 0 Render date: 2024-11-26T10:48:39.477Z Has data issue: false hasContentIssue false
  • English
  • Français

Microscopic Characterization of a Sperm Mutant Line of the Fern Ceratopteris Richardii

Published online by Cambridge University Press:  02 July 2020

Kelly A. Davidson ,
Leslie G. Hickok  and
Karen S. Renzaglia
Kelly A. Davidson
Affiliation:
Department of Plant Biology, Southern Illinois University, Carbondale, IL62901
Leslie G. Hickok
Affiliation:
Department of Plant Biology, Southern Illinois University, Carbondale, IL62901
Karen S. Renzaglia
Affiliation:
Department of Plant Biology, Southern Illinois University, Carbondale, IL62901
Get access

Extract

Mature sperm cells of Ceratopteris richardii are spiraled over three revolutions and contain a locomotory apparatus with approximately 70 flagella attached at the cell anterior (Fig. 1). Abundant organelles are dispersed along the inner surface of an elongated, coiled nucleus (Figs. 1, 3, 8). The cytoskeleton comprises a network of microfilaments that encases the nucleus (Fig. 6) and two distinct microtubule arrays: a microtubular ribbon (spline) and flagella with anchoring basal bodies (Fig. 3). This study uses light, fluorescence, transmission electron (TEM), and scanning electron microscopy (SEM) to characterize cell organization in a motility impaired sperm mutant line of Ceratopteris. Because motility mutations likely involve the cytoskeleton, emphasis was placed on observing microtubule and actin arrays in the mutant compared to wild-type sperm cells. Protocols follow Hoffman and Vaughn for TEM and Schmitt and Renzaglia for SEM. Microfilament arrays in relation to the nucleus were examined by rhodamine-phalloidin and DAPI fluorescence.

Type
Light and Electron Microscopic Techniques for the Study of Plant Pathogenic Fungi and Their Interactions with Host Plants
Information
Microscopy and Microanalysis , Volume 6 , Issue S2: Proceedings: Microscopy & Microanalysis 2000, Microscopy Society of America 58th Annual Meeting, Microbeam Analysis Society 34th Annual Meeting, Microscopical Society of Canada/Societe de Microscopie de Canada 27th Annual Meeting, Philadelphia, Pennsylvania August 13-17, 2000 , August 2000 , pp. 700 - 701
Copyright
Copyright © Microscopy Society of America

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1. Hoffman, J. C., and Vaughn, K. C.. Inter. J. Plant Sci. 156 (1995) 346-35,8.CrossRefGoogle Scholar

2. Schmitt, S. J. and Renzaglia, K. S.. Microsc. Microanal. 5 (Proc. MSA 1999): 1260–1261.CrossRefGoogle Scholar

3. Mainwaring, L. H.. Thesis, East Tennessee State University (1997).Google Scholar

4. Duckett, J. G. et al. Gamete Res. 2 (1979) 320–343.CrossRefGoogle Scholar

5. Dutcher, S. K. et al. J. Cell Biol. 98 (1984) 229–236.CrossRefGoogle Scholar

6. This research was supported by undergraduate research scholarships from the Microscopy Society of America and Illinois Academy of Science, an SIU-C Chancellor's Undergraduate Research/Creative Activity Award, and NSF grant DEB-9527735 (Research Experiences for Undergraduates Program).Google Scholar