01917nam a2200253Ia 4500 MX-MdCICY 20260521091111.0 CICY B-8435 Early.flowering Scots pines through tissue culture for accelerating tree breeding Theoretical and Applied Genetics, 93(5-6), p.840-848, 1996 Scots pine plantlets were produced via tissue culture using cotyledons excised from germinated embryos as ~xplants. The optimum tissue culture conditions were: ~4GD basal medium gelled with agar-Gelrite during shoot formation and with agar during rooting, inclusion of 5.0 btM benzylaminopurine (BAP)and 0.05 pM naphthaleneacetic acid (NAA)for 2 weeks for shoot induction, and repeated 2.7 pM NAA pulses of 1 week for rooting. Micropropagation success was genotype-dependent. Average multiplication rates varied among experiments from 3 to 15 shoots per embryo. The maximum shoot production from a single embryo was 35. Rooting was the most difficult phase in the propagation process. Most of the plantlets had a plagiotrophic and highly branched growth habit when growing in the greenhouse. Some individuals produced megasporangiate strobili at the age of 3 years and microsporangiate strobili with viable pollen at the age of 4 years. Early-flowering clones and the ability to onserve seedlings from which cotyledons have been cultured give new possibilities for accelerated tree breeding. PINUS SYHESTRIS SCOTS PINE TISSUE CULTURE EARLY MATURATION FLOWERING Haggman, H. M. Aronen, T. S. Stomp, A.-M. https://drive.google.com/file/d/1FBShW8tr00a2Q-ODH7uv2jOou-qsniVQ/view?usp=drivesdk Para ver el documento ingresa a Google con tu cuenta: @cicy.edu.mx Loc REF1 250602s9999 xx |||||s2 |||| ||und|d 18678 18678 0 0 Loc 0 0 F1 CICY CICY RE 2025-06-25 0 B-8435 2025-06-25 12:47:20 2025-06-25 REF1