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  • Manihot esculenta  (2)
  • Springer  (2)
  • American Chemical Society (ACS)
  • American Institute of Physics
  • National Academy of Sciences
  • 1985-1989  (2)
Collection
Publisher
  • Springer  (2)
  • American Chemical Society (ACS)
  • American Institute of Physics
  • National Academy of Sciences
Years
  • 1985-1989  (2)
Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Plant cell, tissue and organ culture 6 (1986), S. 221-228 
    ISSN: 1573-5044
    Keywords: Manihot esculenta ; cassava ; propagation ; in vitro propagation ; tissue culture
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A method is presented for the rapid in vitro propagation of cassava (Manihot esculenta Crantz). Nodal explants were induced to grow as multiple-shoot cultures on a medium containing 1.0 μM 6-benzylamino purine (BAP), supplemented with 0.25 μM α-naphthaleneacetic acid (NAA). Nodes were removed from the shoots after three weeks of growth and subcultured on fresh culture medium. An average of 7.0 nodes were produced from each explanted node after three weeks in culture. Nodal explants were transferred to a medium containing 2.5 μM indole-3-butyric acid (IBA) to improve root initiation on the developing plantlets. Plant establishment was possible upon transfer to soil. In vitro propagation offers enhanced rates of multiplication over more conventional methods of propagation. In addition, in vitro propagation facilitates the storage and international exchange of cassava germplasm.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Plant cell, tissue and organ culture 6 (1986), S. 229-234 
    ISSN: 1573-5044
    Keywords: Manihot esculenta ; cassava ; embryo culture ; seed germination
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Cassava fertility and seed viability are frequently low, which can be a disadvantage in a breeding programme. An embryo culture method is described whereby embryonic axes are excised from mature seeds and placed on a culture medium containing 1.23 μM indolebutyric acid (IBA) at 30°C under continuous light. The number of plants recovered by embryo culture was much greater than the number recovered from conventional seed germination procedures.
    Type of Medium: Electronic Resource
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