Crop Science Grow Your Career with CSSA
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Published in Crop Sci 23:268-272 (1983)
© 1983 Crop Science Society of America
677 S. Segoe Rd., Madison, WI 53711 USA
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Rines, H. W.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Rines, H. W.
Agricola
Right arrow Articles by Rines, H. W.

Oat Anther Culture: Genotype Effects on Callus Initiation and the Production of a Haploid Plant1

H. W. Rines2

Calli were initiated from 2,627 of approximately 65,000 anthers of oats (Avena sativa L.) placed on various culture media. One haploid (n = 3x = 21) and two diploid (2n = 6x = 42) plants were recovered from an anther of the cultivar ‘Stout’. These were the first plants known to be producebdy anther culture in oats. Ther elated cultivars Stout and ‘Clintford’ were the source of most of the anthers which formed callus. These lines responded with more than 30% anthers callusing under defined culture conditions, while no other genotypes among over 100 initially tested had more than 6% anthers callusing and most had none. When Clintford was crossed with five nonresponding genotypes, the F1 plants from three of the crosses produced relatively high frequency anther-callusing responses while F1 plants of the other two crosses gave low responses indicating a complex inheritance of the trait. The highest frequency of callusing anthers was achieved with a Stout x Clintford F2 plant where 12 of 15 cultured anthers responded. Murashige and Skoog basal medium with 10% sucrose and no hormonegs ave the highest anther callus initiation frequencies among media tested, but the only anther to produce plants had been initially plated on a modified potato extract medium containing 2 mg/ liter 2,4-dichlorophenoxy acetic acid and 0.5 mg/liter kinetin. This anther had also been heat-shocked at 35 C for 24 hours immediately after plating and prior to standard incubation at 22 C. Cold shocks reduced sucrose levels, and the addition of various growth substances had either no or detrimental effects on callus initiation frequencies and did not promote plant differentiation. Means to regenerate plants from initiated calli on a consistent basis are needed to make oat anther culture a useful technique.

Key Words: Cereals • Tissue culture • Allopolyhaploid • Androgenesis • Avena sativa L


1 Joint contribution of USDA-ARS and the Minnesota Agric. Exp. Stn. Paper No. 12,061, Scientific Journal Series, Minnesota Agric. Exp. Stn.

2 Research geneticist, USDA-ARS, and associate professor, Dep. of Agronomy and Plant Genetics, Univ. of Minnesota, St. Paul, MN 55108.

Received for publication January 25, 1982.





HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
The SCI Journals Agronomy Journal Vadose Zone Journal
Journal of Plant Registrations Soil Science Society of America Journal
Journal of Natural Resources
and Life Sciences Education
Journal of
Environmental Quality
Copyright © 1983 by the Crop Science Society of America.