Movement and distribution of 14C-indole-3-acetic acid in branches and rooted cuttings of Douglas-fir

The transport of ¹⁴C-indole-3-acetic acid in branch terminals and stems of rooted cuttings of Pseudotsuga menziesii (Mirb.) Franco was studied to determine if the plagiotropic growth of cuttings might result from an accumulation of basipetally transported auxin in the morphologically upper side of cuttings stems. Twenty-four h after application of 10 μl of ¹⁴C-IAA solution to the cut surface of decapitated, rooted cuttings, nearly twice as much activity was detected in extracts of tissue from the morphologically upper than from the lower halves of the stems. A similar distribution of activity was observed in horizontal branch terminals and in branch terminals which had been tied vertically for 2 weeks. The magnitude of the difference in activity between the 2 sides of the stem was greater in the horizontal than in the vertical branches.
There was no significant difference in transport through the upper and lower sides of excised stem segments from cuttings or branch terminals. In segments from rooted cutting stems, however, significantly more radioactivity from ¹⁴C-IAA donor blocks was detected in the lower than in the upper halves of segments.     

Age- and position-of-origin and rootstock effects in Douglas-fir plantlet growth and plagiotropism

Plagiotropic angle of seedling-derived Douglas-fir plantlets varied with position of adventitious bud origin on the explanted cotyledon rosette, being least at its center (18°) and greatest (45°) along the basal third of the cotyledon. When the tops of plagiotropic plantlets (55°) were grafted to seedling rootstock, they assumed a near-vertical orientation (10°), with pectinate changed to radial leaf arrangement, within 5 months. Conversely, seedling tops grafted to plagiotropic plantlet rootstock grew plagiotropically (56°). These, and other observations lead to a hypothesis that plagiotropism in cotyledon-derived plantlets results in part from an incomplete vascular connection of the root system to the shoot.In contrast, the greater plagiotropic angle in plantlets from a 12 year-old tree, decreased by only half (from 72° to 34°) after grafting to seedling rootstock. First-season height increment of these plantlets was only 60 percent of seedling or juvenile plantlet height increment, and was unaffected by rootstock type. The adult-origin plantlets exhibited mature shoot morphology, and unchanged plagiotropism after 2 years growth in large pots. Thus it appears that the culture-induced juvenile appearance and behaviour noted for this material when maintained in vitro, is dependent on the continued presence of the culture conditions.     

Micropropagation of adult Swainsona formosa (Leguminosae: Papilionoideae: Galegeae)

Summary Explants of axillary buds excised from mature adult stems of Swainsona formosa (G. Don) J. Thompson (syn. Clianthus formosus) were cultured on Murashige and Skoog medium supplemented with a range of auxins, cytokinins, and sucrose concentrations. Auxins did not increase shoot or bud numbers above controls, and 2,4-dichlorophenoxyacetic acid was the only auxin to significantly increase callus production. Benzyladenine or thidiazuron incorporated into the medium at 0.1 μM stimulated shoot and bud production, and shoot growth occurred following removal of cytokinins from the medium after 4 wk. Shoot number increased linearly with sucrose concentration up to 40 g l⁻¹, but shoot height and the number of cytokinin-induced buds were optimal at sucrose levels of 20–30 g l⁻¹. Roots were initiated in vitro following treatment of cuttings with 0.1% indole-3-butyric acid and 0.1% α-naphthaleneactic acid. Plantlets were successfully established in soil but were plagiotropic and exhibited distichous phyllotaxy.     

Elongation, rooting and acclimatization of micropropagated shoots from mature material of hybrid larch

Factors were defined for elongation, rooting and acclimatization of micropropagated shoots ofLarix x eurolepis Henry initiated from short shoot buds of plagiotropic stecklings serially propagated for 9 years from an 8-year-old tree. Initiation and multiplication were on Schenk and Hildebrandt (SH) medium supplemented with 5 M 6-benzyladenine (BA) and 1 M indole-butyric acid (IBA). Stem elongation was obtained in 36% of the shoots on SH medium containing 0.5 M BA and 63% of the remaining non-elongated shoots initiated stem elongation after transfer on SH medium devoid of growth regulators. Rooting involved 2 steps: root induction on Campbell and Durzan mineral salts and Murashige and Skoog organic elements, both half-strength (CD-MS/2), supplemented with 1 M of both naphthaleneacetic acid (NAA) and IBA, and root elongation following transfer to CD-MS/2 medium devoid of growth regulators. Repeating this 2-step sequence yielded up to 67% rooted shoots. Acclimatization of plantlets ranged from 83% to 100%. Over 300 plants were transferred to the greenhouse; some showed plagiotropic growth.     

Frequency of somaclonal variation in plants of black spruce (Picea mariana,Pinaceae) and white spruce (P. glauca,Pinaceae) derived from somatic embryogenesis and identification of some factors involved in genetic instability

Plants of black spruce (Picea mariana, N = 7047 individuals) and white spruce (P. glauca, N = 3995 individuals) were regenerated from a total of 87 clones over a 5-yr period by somatic embryogenesis to study factors that might be associated with the appearance of variant phenotypes. Morphological evaluation of the plants showed several types of variation. These variations were grouped into nine types: dwarfism (type A), reduced height with various form anomalies (types B, C, and D), needle fasciation (type E), abnormality in tree architecture (type F), variegata phenotype (type G), and plants with an overall regular morphology but smaller than normal plants (type H). Plagiotropic plants were also observed (type I). Each plant from types A to H (except type C where no plants survived more than 6 mo) had retained its phenotype over 4–5 yr of growth. Some of the variant types could be related to chromosomic instability: chromosome counts showed aneuploid cells for type-A and type-D plants. The type I (plagiotropism) was not related to genetic instability but rather to physiological disorders. In total, spruce variants of types A–H were obtained at relatively low frequencies, i.e., 1.0% (39/3995) for white spruce and 1.6% (110/7047) for black spruce. Statistical analyses, conducted with family, clone, and time in maintenance as variables, showed that clone was the most important source of genetic instability followed by time in maintenance.     

Rooting and establishment of Calabrian pine plantlets propagated in vitro: influence of growth substances, rooting medium and origin of explant

The effect of auxins and a cytokinin on induction of roots in cultured axillary shoots of Pinus brutia Ten, has been tested. Auxin was crucial for root initiation and the rooting response varied according to the type and concentration of auxin applied. Both auxin and cytokinin and the interactions between them affected the quantity and quality of the induced roots. Aerated non-sterile tap water was an effective rooting medium, comparable to agar. After planting out into soil, some of the influences of auxin and cytokinin could still be seen after six months. However, roots developed normally in the soil, displaying dichotomous lateral branches. The results draw attention to the need for care in the choice and application of the medium for the initial induction of roots. Results of greenhouse trials indicated that the most vigorous plants were obtained via the axillary shoots.     

Special symposium: In vitro plant recalcitrance recalcitrance of woody and herbaceous perennial plants: Dealing with genetic predeterminism

Summary As a general, long-lived perennial plants probably present the most challenging obstecles to the researcher, breeder or propagator utilizing microculture as a tool. These challenges appear during all stages of the microculture process, but are probably most resplendent during the stabilization phase. What may be particularly frustrating is that much of this ‘recalcitrance’ is genetically driven and is thus difficult to control by environmental and nutritional manipulations in microculture. Perennials have complex seasonal cycles and life cycles, which complicate control of their growth in microculture. As shoot cultures have provided useful tools for overcoming these limitations, the inability to establish stabilized shoot cultures is a major form of recalcitrance. Plants having seasonal growth dynamics dominated by strong episodic or determinant shoot growth are some of the most recalcitrant species because stabilized shoot cultures cannot be readily generated. In some cases, episodic growth may be tied closely to phase state and can thus be controlled by manipulating phase; nevertheless, adequate controls have not been identified for many problematic plants. Another trait contributing to recalcitrance of perennials is the relatively slow growth rate in microculture. Slow growth complicates such procedures as selection of transformed tissues. The high phenolic content of many perennial tissues can interfere with the efficacy of transgenic traits such as β-glucuronidase. Developmentally determined growth characteristics such as plagiotropism may persist through all stages of microculture and complicate the recovery of commercially useful micropropagules. Although some technical approaches can occasionally circumvent immediate microculture limitations, general solutions await the development of a deeper understanding of physiological bases of such genetically predetermined phenomena.