1981
DOI: 10.1139/b81-121
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In vitro studies of adventitious shoot formation in Pinus contorta

Abstract: Isolated embryos of Pinus contorta Dougl. ex Loud, were induced to form adventitious buds on a cytokinin-supplemented medium. Further development of the buds required transfer to a cytokininless medium. Both bud induction and development were stimulated by a dilution of the basal culture medium and best growth was obtained if the buds were isolated from the original tissue when stem elongation had started. The growth of these isolated adventitious shoots was further stimulated by adding activated charcoal to t… Show more

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Cited by 278 publications
(75 citation statements)
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“…The positive effect of activated charcoal on shoots has also been found by many other workers (Mehra-Palta et al, 1978;Von Arnold and Eriksson, 1981;David et al, 1982). The unexpected bud formation on BIMI free of growth regulators (table I) was concluded to be an after-effect of foliar spraying on mother plants (Scaltsoyiannes, 1988).…”
Section: Rooting Of Shootssupporting
confidence: 68%
“…The positive effect of activated charcoal on shoots has also been found by many other workers (Mehra-Palta et al, 1978;Von Arnold and Eriksson, 1981;David et al, 1982). The unexpected bud formation on BIMI free of growth regulators (table I) was concluded to be an after-effect of foliar spraying on mother plants (Scaltsoyiannes, 1988).…”
Section: Rooting Of Shootssupporting
confidence: 68%
“…Seeds were sterilized in 20% (v/v) commercial bleach for 20 min and rinsed three times with sterile water. Dissected embryos were placed on induction (von Arnold and Eriksson [AE]) medium (von Arnold and Eriksson, 1981) containing 10 mol L Ϫ1 2,4-D, 5 mol L Ϫ1 N 6 -benzyladenine, 5% (w/v) Suc, and 0.8% (w/v) Bacto-agar, pH 5.8 (DIFCO Laboratories, Detroit). The stock culture was maintained in the dark at 26°C for 4 to 5 weeks.…”
Section: Plant Materialsmentioning
confidence: 99%
“…The seeds were then disinfested in a flow cabinet with 2.0% (v/v ) NaOCl for 20 min, followed by three rinses with sterile water. Afterwards, zygotic embryos were excised from seeds and inoculated in test tubes (22×150 mm) containing 10 mL of LPm culture medium (von Arnold and Eriksson 1981), supplemented with Morel vitamins (Morel and Wetmore 1951), glutamic acid (8 mM), 2,4-dichlophenoxiacetic acid (2,4-D; 20 μM), maltose (3%; w/v), and Difco™ agar (0.7%; w/v). The pH of the culture medium was adjusted to 5.8 prior to autoclaving at 121°C, 120 kPa for 15 min.…”
Section: Methodsmentioning
confidence: 99%