The structure and developmental patterns of inflorescence of longan (Dimocarpus longan Lour.) were studied microscopically and by the naked eye. In inflorescence of longan, compound dichasia are arranged on three to four orders of monopodial axes without the formation of terminal flowers, indicating that longan inflorescence is pleiothyrse; cymose partial inflorescences are arranged on more than two monopodial axes. Most of the monopodial axes had differentiated by the end of November just before the cool season. The first sign of inflorescence formation was the appearance of bract primordia at apical meristems of the preformed monopodial axes, with lateral axes preceding the main axes. Dichasia were formed in the axils of bract primordia, and the formation of bracts and dichasia continued. Bract appearance can be detected by the naked eye 1 week after microscopically detected bract appearance. Shoots with intermediate characteristics between the inflorescence and the vegetative shoots were formed; dichasia were formed on the lateral axes, but not on the main axes in intermediate shoots. These results suggest that apical meristems on the terminal shoot produce monopodial axes, together with foliage leaf primordia, before floral induction, but produce bract primordia and compound dichasia, which are composed of sympodial axes, after floral induction.
Miki Nakata, Nobuo Sugiyama, and Tanachai Pankasemsuk
Samuel Salazar-García, Elizabeth M. Lord, and Carol J. Lovatt
The developmental stage at which the shoot primary axis meristem (PAM) of the `Hass' avocado (Persea americana Mill.) is committed to flowering was determined. Three-year-old trees were subjected to low-temperature (LT) treatments at 10/7 °C day/night with a 10-h photoperiod for 1 to 4 weeks followed by 25/20 °C day/night at the same photoperiod. Before LT treatment, apical buds of mature vegetative shoots consisted of a convex PAM with two lateral secondary axis inflorescence meristems lacking apical bracts each associated with an inflorescence bract. Apical buds did not change anatomically during LT treatment. However, the 3- and 4-week LT treatments resulted in inflorescences at 17% and 83% of apical buds, respectively. Trees receiving 2 weeks or less LT, including controls maintained at 25/20 °C, produced only vegetative shoots. Apical buds of 2-year-old trees receiving 3 weeks at 10/7 °C plus 1 week at 20/15 °C produced 100% inflorescences. GA3(100 mg·L-1) applied to buds 2 or 4 weeks after initiation of this LT treatment did not reduce the number of inflorescences that developed. `Hass' avocado apical buds were fully committed to flowering after 4 weeks of LT, but were not distinguishable anatomically from those that were not committed to flowering.
Charlotte M. Guimond, Preston K. Andrews, and Gregory A. Lang
Flower initiation and development in `Bing' sweet cherry (Prunus avium L.) was examined using scanning electron microscopy. There was a 1- to 2-week difference in the time of initiation of flower buds on summer pruned current season shoots (P) compared to buds borne on unpruned shoots (U) or spurs (S). By late July, this difference was obvious in morphological development. The P buds had already formed floral primordia, while the S and U buds showed little differentiation in the meristem until early August. In general, buds from unpruned shoots were similar developmentally to spur buds. By late August, primordial differentiation was similar in the buds from all the wood types; however, buds from pruned shoots were significantly larger (838 μm) than buds from spurs (535 μm) and unpruned shoots (663 μm). Early summer pruning may shift allocation of resources from terminal shoot elongation to reproductive meristem development at the base of current season shoots. The similarity in reproductive bud development between spurs and unpruned shoots, given the difference in active terminal growth, might suggest that developmental resources are inherently more limiting in reproductive buds on spurs.
Merle M. Millard, Dehua Liu, Michael J. Line, and Miklos Faust
Magnetic resonance imaging estimates unreasonably high T2 times when creating T2 images in woody plants when tissues contain a limited amount of water. We developed a system to correct such images. Tissue distribution of proton density and states of water were determined by creating images of proton density and T2 relaxation times in summerdormant (paradormant) apple (Malus domestica Borkh.) buds. These images reveal that the proton density and water states obviously are not distributed uniformly in the bud and stem; but, the distribution of water depends greatly on the tissue type (bark, xylem, or meristem of the stem), and there are differences in the states of water even within the same tissue. At low proton density T2, calculated relaxation times were unreasonably high in tissues, with the exception of meristem of the shoot. In buds that were induced to grow and in which proton density was higher, T2 times appeared as expected. Variance of T2 times in tissues containing little water was 50 times higher than in those with a higher water content. Data with such high variance were excluded from the images; thus, the image was “corrected.” Corrected images of T2 times fit the distribution of water indicated by the proton density images well.
J.W. White, H. Chen, X. Zhang, D.J. Beattie, and H. Grossman
Floral initiation and development of greenhouse and growth room-grown Aquilegia × hybrida Sims cultivars were studied using a scanning electron microscope. All greenhouse-grown cultivars initiated floral buds before cold treatment, ≈ 5 months after sowing. Floral initiation occurred at the apical meristem and proceeded acropetally on an elongated conical axis in the sequence: sepals, petals, stamens, stamenodia, and carpels. In a second experiment, 13 Aquilegia cultivars, three of which had been used in the first experiment, were grown as seedlings in a growth room at 20C under an 8-, 12-, 16-, or 20-hr photoperiod, each totaling 10.2 mol·day-1·m-2 irradiance from cool-white fluorescent lamps. Here, floral initiation was absent even after 7 months from sowing, presumably because there was no diurnal variation in irradiance or temperature.
Azza Abdel-Aziz Tawfik and P. E. Read
Regeneration from callus of rosemary has not been reported. Leaf segment, meristem-tip and shoot-tip explants of Rosmarinus officinalis were cultured on a Murashige and Skoog (MS) medium supplemented with five concentrations of the cytokinin thidiazuron (TDZ) alone or in combination with 3-indoleacetic acid (IAA). Callus was formed on the base and leaves of the shoottips after 6 weeks when cultured under cool white fluorescent light (26 u mol·S-1 m-2) on MS containing 0.5, 1.0, 1.5 or 2.0 mg/l TDZ. Calti were transferred to fresh MS medium supplemented with 0.2, 0.4, 0.6, 0.8 or 1.0 mg/l TDZ or 2.0, 4.0, 6.0 or 8.0 mg/l benzyladenine (BA) where shoot formation occurred. Essentiality of IAA was not clear from these experiments and further research is underway to refine regeneration protocol
Carole H. Saravitz, Frank A. Blazich, and Henry V. Amerson
Hypocotyls of Fraser fir (Abies fraseri (Pursh) Poir.) were excised from seeds germination 9 days and placed on bud induction medium containing 10 mg/liter benzyladenine (BA) and 0.01 mg/liter naphthaleneacetic acid (NAA) or medium without growth regulators. After 3 days on medium containing growth regulators, cell divisions were localized in epidermal and subepidermal layers of the hypocotyl while similar cell divisions were not observed in control-treated hypocotyls. Cell clusters consisting of two to five cells were present after 7 days in hypocotyls placed on bud induction medium. In control-treated hypocotyls, stomata continued to develop and cells within the cortex became vacuolated during the first 2 weeks in culture. All hypocotyls were transferred to secondary medium after 3 weeks. Cell clusters continued to enlarge into meristemoids in hypocotyls initially placed on bud induction medium. Gradually, meristemoids developed into buds and cataphylls were observed covering bud meristems.
Terri Woods Starman
Manually pinched plants of 18 cultivars of Impatiens hybrids (Keintzler New Guinea impatiens) were compared to control plants to determine the effect of apical meristem removal on flowering, growth and branching. Pinching delayed days to anthesis (first flower) of all cultivars, however, further delay in days to marketability (5 flowers open) was dependent upon cultivar. Plant area and fresh and dry weight were not affected by pinching plants of any cultivar. Cultivar influenced response to pinching treatments for plant height and plant width. Secondary branch number was increased by approximately 3 branches for all cultivars when plants were pinched. There were interactions between cultivar and treatment for primary, tertiary, and total branch number. Measured improvements in plant form determined two cultivars, Sylvine and Thecla, should be pinched. Chemically pinching these two cultivars with dikegulac at 780 mg·liter-1 was comparable to manually pinching plants.
Jeffrey W. Adelberg, Bill B. Rhodes, Halina T. Skorupska, and William C. Bridges
Adventitious and axillary shoots of melon (Cucumis melo L.) were cultured from explants on a modified Murashige and Skoog medium containing 10 μm BA. Explants were diversified with regard to genetic source (breeding lines Miniloup, L-14, and B-line), seed parts (apical and cotyledon tissue), seed maturity (10-40 days after pollination; DAP), and cotyledon sections with respect to apical-radicle axis (distal and proximal). Plants were screened for ploidy level by pollen morphometry. Immature cotyledons produced more tetraploid regenerants than mature cotyledons from seed of breeding line Miniloup; the highest frequency of tetraploid regenerant plants was from cotyledons of embryos harvested 18 and 22 DAP. Explants from the apical meristem of the same seeds produced fewer or no tetraploid plants. Proximal sections from immature cotyledons of three genotypes (Miniloup, L-14, B-line) produced higher frequencies of tetraploids than whole mature cotyledons or whole immature cotyledons.
Richard L. Harkess and Robert E. Lyons
A study was undertaken to determine the rate of floral initiation in Rudbeckia hirta. R. hirta plants were grown to maturity, 14-16 leaves, under short days (SD). Paired controls were established by placing half of the plants under long days (LD) with the remainder left under SD. Beginning at the start of LD (day 0), five plants were harvested daily from each photoperiod group for twenty days. Harvested meristems were fixed in 2% paraformaldehyde - 2.5% glutaraldehyde in 0.1 M sodium cacodylate buffer (pH 7.0) for 24 hrs, dehydrated in an ethanol series, embedded in paraffin and sectioned at 8 μm. Serial sections were stained with Methyl-green Pyronin, with adjacent sections treated with RNase for nucleic acid comparison. All events of floral initiation were identified, The results of limited inductive photoperiod indicate that 16-18 LD were required for flowering.