Effects of gibberellins and benzylandenine on dormancy and flowering of Lilium speciosum

GA_{4 + 7} (1000 mg/l), alone or in combination with BA (100 mg/l), was found to induce shoot emergence and flowering in dormant bulbs of L. speciosum, while GA₃, alone or in combination with BA, had no effect. BA had a significant influence on increasing flower numbers, particularly when combined with GA_{4 + 7}.     

The Effects of Some Growth Regulators on Peach Flower Bud Abscission

Applications of growth regulators to detached peach laterals in winter had variable effects on flower bud abscission. GA₃ and GA₄₊₇ increased bud abscission while IAA, BA and ABA inhibited abscission. Ethephon had a variable effect. Interactions were obtained between the compounds generally with IAA or GA playing the major role. GA had a peak of activity during a critical period in late winter indicating a variation in responsiveness. Variations in sensitivity to GA were obtained for different cultivars. Field applications of GA₃, GA₄₊₇, and ethephon to Elberta peach trees in winter, alone and in various combinations, promoted bud abscission.     

Effect of exogenous growth regulators on flowering and cytokinin levels in azaleas

‘Alaska’ and ‘Redwing’ azaleas having dormant flower buds were sprayed with gibberellins (GA₃ or GA_{4 + 7}) alone and in combination with thiourea, N⁶ benzyl adenine (BA) or kinetin weekly for 3 or 4 weeks to test the efficacy of these materials in breaking bud dormancy. Additional plants received 6 weeks of cold storage at 4.5°C or glasshouse day temperatures of 21°C and above. The 2000 and 3000 mg l^?1 GA₃ and Ga_{4 + 7} sprays were better than 1000 mg l^?1 in promoting flowering, with ‘Redwing’ responding better than ‘Alaska’. GA-treated plants flowered in fewer days than those receiving cold storage. Flower diameter and pedicel length increased with higher levels of GA, and flower uniformity was comparable to cold-stored plants on most GA-treated ‘Redwing’-plants. Thiourea, BA and kinetin applied alone had no effect and considerable cytokinin activity was highest in GA-treated buds 14–21 days after treatment application. No increase in activity occurred on plants not receiving GA.     

珍稀濒危植物珙桐离体快繁技术初步研究

 研究了我国一级珍稀濒危树种珙桐(Davidia involucrata Baill.) 带芽茎段的离体培养。筛选出最佳培养基: ( 1) 冬芽诱导培养基: WPM+BA 2.0 mg·L^-1+NAA 0.1 mg·L^-1; (2) 丛生芽诱导培养基: WPM + BA 2.0 mg·L^-1; (3) 丛生芽增殖培养基: WPM+ BA 2.0 mg·L^-1+ ZT 0.1 mg·L^-1; (4) 生根培养基: WPM + NAA 0.5 mg·L^-1。     

Comparison of shoot induction ability of different explants in herbaceous peony (Paeonia lactiflora Pall.)

Shoot induction ability of explants of herbaceous peony was investigated in semisolid MS medium containing BA, TDZ and GA₃. Callus was readily induced from stem without node and petiole explants within 2 days of culture but failed to generate shoots. Adventitious shoots were successfully produced from meristematic regions only: bud eyes on nodal stem sections, and junctions of petioles and petiolules. No shoots were induced from internode sections, petiole without junctions, or leaf sections. Nodal sections were the most efficient explants. There were up to 20 shoots in one explant generated within 20 days of culture. TDZ was more effective than BA to induce shoots. The 100% shoot induction rate was obtained in medium containing 0.1–3 mg L⁻¹ of TDZ. However, higher concentrations of TDZ inhibited shoot elongation and only large leaf clusters were produced. Combinations of BA and TDZ failed to increase shoot induction rates but caused shoots shorter. The 2–60-min pretreatment of explants with 20 mg L⁻¹ TDZ solution was very effective to induce adventitious shoots directly, but both shoot number and shoot length tended to decrease as treatment time increased. GA₃ was beneficial for shoot and stem elongation.     

Factors affecting the growth of in vitro cultured lateral buds from Phalaenopsis flower stalks

Phalaenopsis flower-stalk buds cultured in vitro show 3 modes of growth: dormant, vegetative and reproductive. The effects of bud position on the stalk, temperature, and benzyladenine (BA) on the mode of bud growth were examined.Flower stalks were cut into 1-node sections, each with 1 bud, and inserted into solid culture medium, top side up. Buds on the upper sections had a tendency to remain dormant regardless of temperature. Sprouting buds placed at 20°C or 25°C showed reproductive growth except for some on the basal sections which grew vegetatively. At 28°C, all buds developed vegetatively independent of their original position on the stalk. The buds on the sections taken from both stalks which had elongated at min 18°C and min 28°C were subcultured; the mode of growth of the cultured buds was not affected by the temperature during flower-stalk elongation but was affected by the subsequent culture temperature.Cultured buds which had remained dormant were stimulated to sprout by addition of BA to the medium. At 5 p.p.m. and above, all buds began to develop, but malformations developed on the leaves of the shoots. All factors considered, BA at 2.5 p.p.m. was found to be the optimum level. The further development of the buds released from dormancy by BA was also affected by the position on the flower stalk and by cultural temperature.     

Effects of cold storage on postharvest leaf and flower quality of potted Oriental-, Asiatic- and LA-hybrid lily cultivars

The effects of cold storage of mature potted plants on postharvest leaf and flower quality were investigated in several cultivars of three major groups (Oriental, Asiatic and LA) of hybrid lilies (Lilium spp.). Mature plants were stored in darkness at 3 °C for 2 weeks before placing them in a postharvest evaluation room (22 °C) and were compared with plants moved directly to the evaluation room. The efficacy of GA₄₊₇ plus benzyladenine (BA) treatments (applied just before cold storage) for preventing cold-induced postharvest disorders in each cultivar was also evaluated. In all cultivars, cold storage caused several adverse effects on postharvest quality, including accelerated leaf yellowing or browning, bud abortion and reduced flower or inflorescence longevity. Leaf abscission was observed only in Oriental-hybrids. Treatment with GA₄₊₇ plus BA significantly reduced these disorders and improved the overall postharvest quality after cold storage. While different cultivars differed greatly in their sensitivity to cold storage, all the cultivars benefited from GA₄₊₇ plus BA treatment. Experiments indicated that GA₄₊₇ plus BA treatments could be applied as early as 2 weeks before the mature bud stage without compromising the positive effects.     

Vegetative and floral bud abortion in cucumber plants: Hormonal and environmental effects

The acropetal, zonal pattern of axillary buds along the main shoot of the cucumber plant, which includes bare nodes (no appreciable development), staminate, mixed and, lastly, pistillate (or hermaphrodite) ones, is described in monoecious, gynoecious, andromonoecious and hermaphrodite genotypic lines grown at various seasons and treated with gibberellin (GA_{4 + 7}) or with an ethylene-releasing compound (CEPA, 2-chloroethyl phosphonic acid).Under optimal growing-conditions, GA given to gynoecious and hermaphrodite plants mimicked summer conditions by increasing the number of basal bare nodes and the proportion of abortive female buds and staminate buds. CEPA given to monoecious and andromonoecious plants generally imitated winter conditions by decreasing the proportion of bare and abortive nodes, and increasing female tendency.Bud abortion was also noticed under sub-optimal growing-conditions (low light intensities and relatively low temperatures) during the winter. This seems to be physiologically unrelated to the above mentioned phenomena.     

Factors affecting in vitro adventitious shoot formation on internode explants of Citrus aurantium L. cv. Brazilian

The in vitro formation of newly formed adventitious buds and shoots from internodal branch segments was studied on 12-month-old plants of Citrus aurantium L. cv. Brazilian. The effects of 6-Benzyladenine (BA) and α-Naphthalene acetic acid (NAA) treatments were evaluated on adventitious bud and shoot regeneration. High rates of bud initiation and shoot development were obtained both with BA supplemented medium, in the range from 1 mg L⁻¹ to 3 mg L⁻¹, and with 0.1 mg L⁻¹ NAA supplemented medium. NAA concentrations above 1 mg L⁻¹ significantly reduced bud initiation and shoot elongation. The results obtained using different in vitro culture vessels such as Petri dishes, tubes and glass culture jars were compared. The highest adventitious bud induction was observed in Petri dishes for internodes cultured in 2 mg L⁻¹ BA supplemented medium, with 95% responsive explants forming 9.0 ± 2.4 adventitious buds. The adventitious buds observed in Petri dishes reached a maximum height of 1 mm, with no further development, while some of the adventitious shoots cultured in tubes and glass culture jars grew over 1 cm in height. A shoot regeneration gradient of the internodes collected along the branch axis was noticed, with basal ones exhibiting higher regeneration frequency.     

Endogenous gibberellins and their effects on flowering and stem elongation in cabbage (Brassica oleracea var. capitata)

Summary

Endogenous gibberellins were extracted from cabbage shoots and were analysed using gas chromatography and mass spectrometry. Nine gibberellins (GA₁, GA₁₉, GA₂₀, GA₄₄, GA₁₂, GA₄, GA_15, GA₂₄ and GA₂₅) were identified. Two gibberellin biosynthesis pathways were suggested, an early-13-hydroxlyated pathway and a non-13-hydroxylated pathway, to operate in cabbage shoots. GA₁, GA₄ and prohexadione calcium, a gibberellin biosynthesis inhibitor, were applied to the shoot tip of cabbage ‘Sousyu’ and ‘Kinkei No.201’ with or without cold treatment. Without cold treatment, stem elongation was increased by gibberellins and was suppressed by prohexadione calcium in both cultivars. But prohexadione calcium treatment, followed by gibberellin, promoted stem elongation more than gibberellin alone. Flowering was not induced by gibberellin or prohexadione calcium without cold treatment. When gibberellin and prohexadione calcium were applied during a cold treatment, stem elongation after the cold treatment was increased by gibberellins and was suppressed by prohexadione calcium in both cultivars. Flower bud appearance was promoted by GA₁ and GA₄ in ‘Sousyu’, but in ‘Kinkei No. 201’ only GA₄ was markedly effective. Inhibition of stem elongation and delay of flower bud appearance by prohexadione calcium were overcome by applying GA₁ or GA₄. Neither gibberellin nor prohexadione calcium treatment changed the number of leaf nodes at anthesis. These results indicated that stem elongation and flower bud development are regulated by gibberellins, but gibberellins might have little effect on flower induction.     

Direct shoot organogenesis on shoot apex from seedling explants of Capsicum annuum L.

In vitro direct multiple shoot formation from seedling explants of Indian high pungent varieties of Capsicum annuum cv. Arka Abhir (AA) and Arka Lohit (AL) was successfully obtained. We were able to induce regeneration potency in these varieties by inverting the explant. Aseptically grown seedling explants with decapitated roots, apical meristem and cotyledonary leaves were inoculated in an inverted position in bud induction medium comprising of Murashige and Skoog's basal medium supplemented with 2-(N-morpholine) ethanesulphonic acid (MES) buffer along with 26.63 μM benzyl adenine (BA), 2.28 μM indole-3-acetic acid (IAA) and 10 μM silver nitrate. Profuse shoot bud induction with 20–25 shoot buds per explant was obtained. Supplementation of phloroglucinol in the bud induction medium resulted in 17 and 18% enhancement in bud induction response in Arka Abhir and Arka Lohit variety, respectively on the inverted hypocotyls. Auxin transport inhibitor tri-iodo benzoic acid (TIBA) in the bud induction medium resulted in induction of buds in a shorter period of 40–45 days when compared to bud induction (BI) medium which takes 55–65 days for bud induction. These buds were transferred to MS medium containing 2.8 μM gibberellic acid and 10 μM silver nitrate resulting in elongation of shoot buds. Transfer of shoots to MS basal medium induced rooting to produce plantlets. This protocol can be efficiently used for mass propagation and presumably also for regeneration of genetically transformed C. annuum tissues.     

Growth and regeneration of plantlets in callus cultures of pineapple

Callus cultures were established from the basal region of in vitro-obtained shoot buds on MS medium supplemented with CH + CW + NAA. Such callus cultures, when grown on MS medium devoid of any growth regulators, regenerated shoot buds and optimum regeneration was obtained on MS + CW (5% v/v) medium. Addition of BA did not enhance shoot bud regeneration, but two variants (albino types) were observed among the BA-induced regenerants. The callus-regenerated shoot buds produced multiple shoots when transferred to MS + NAA + IBA + K medium. The plantlets were induced to root on a modified White's medium + NAA + IBA and subsequently transferred to soil.     

The Influence of Foliar Applications of GA3 GA4,7 and PBA on Breaking Flower Bud Dormancy on Azalea CVS Redwing and Dogwood

Foliar applications of gibberellins (GA₃, GA₄,₇) and 6-benzylamino-9-(2-tetra- hydropyranyl)-9H-purine (PBA) were compared with untreated controls and the conventional low temperature treatment for breaking flower bud dormancy. GA₃ and GA₄, ₇ were compared for their role in promoting flower development. Treatments were initiated when microscopic examination showed the flower buds had reached Stage 6 (style elongated and closed). Plants that did not receive a dormancy-breaking treatment failed to reach anthesis. Application of GA₃ or GA₄, ₇ hastened flowering and increased flower size and pedicel length.     

In vitro micropropagation of the ornamental prickly pear cactus Opuntia lanigera Salm–Dyck and effects of sprayed GA3 after transplantation to ex vitro conditions

We established the conditions to micropropagate the ornamental prickly pear cactus Opuntia lanigera Salm–Dyck through axillary shoot development from isolated areoles. For the shoot proliferation stage different explant orientation (vertical and horizontal), type of cytokinin (BA, DAP and K), and concentrations (0, 1.25, 2,5, 5.0 and 7.5 mg/L) were evaluated. Media [Murashige, T., Skoog, F., 1962. A revised medium for rapid growth and bioassays with tobacco cultures. Phys. Plant. 15, 473–497: 50 and 100%], and carbohydrate concentration (0.25, 0.5, 0.75 and 1.0%) were studied to optimize individual shoot growth and elongation. Following micropropagation and plantlet acclimatization, the effects of GA₃ on plant growth were determined by spraying a series of increasing concentrations (0, 150, 300 and 450 ppm). A reliable and efficient protocol of micropropagation was established for this particular plant species. The greatest propagation ratio (shoot proliferation) was obtained when explants were cultured in vertical orientation (4.975 shoots per explant) as compared to horizontal position (3.692 shoots per explant). The addition of BA to the media resulted in increased shoot number per explant (8) in comparison to K and DA, which produced only 2 shoots in average. However, after 42 days of culture, significantly higher shoot length was obtained with DAP (14 mm) compared to K and BA (4 mm). After the shoot proliferation stage, an elongation subculture was performed prior rooting in which shoot growth was enhanced when crowns of shoots were cultured in 50% of basal salt formulation of Murashige and Skoog (1962) and low sucrose concentration (2.5 and 5%). Exogenous application of GA₃ after plantlet acclimatization on glasshouse conditions increased spine-hair (developed from areoles in young plants) length as part of short-term effects. However, significantly higher values were obtained in plantlets treated with 300 ppm of GA₃ when compared with the rest of the treatments. At the end of the study, the most important long-term effect produced by GA₃ was the suppression of total shoot growth. The micropropagation protocol described here and the conditions to grow the plants through fertigation plus the application of GA₃ that induced changes in the phenotype may be used in commercial exploitations to regenerate 12,500 plantelts in average after 12 months of culture and produce healthy plants with better ornamental characteristics and higher commercial value.     

Cold treatments enhance responsiveness to gibberellin in stock (Matthiola incana (L.) R. Br.)

Summary

Endogenous GAs have been suggested as regulators of stem elongation and flowering of cold-requiring plants. Here, the relationship between temperature conditions and responsiveness to GA₄ on stem elongation and flowering of stock (Matthiola incana) was investigated. The optimum temperature for induction of flower bud initiation was 10°C, and the minimum duration was 20 d in the late flowering cv. Banrei; the type of cold treatment effect on flowering was classified as a “direct effect”. Stem elongation was markedly promoted by cold treatment regardless of flower bud initiation. The cold treatment amplified the stem elongation response to GA₄. The GA₄ level necessary for flower bud initiation was lower in the 10°C treatment than in the 15°C treatment, and it became lower at longer durations of cold treatment. These results indicate that the cold treatments enhance responsiveness to GA₄ not only in the stem elongation process but also in the flower bud initiation process and that the development of responsiveness to GA₄ may correlate with the temperature and duration of cold treatment.     

辣椒子叶高效植株再生体系的建立

 以双丰等17 个辣椒品种为试材, 探讨了不同基因型、激素组合、有机成分及AgNO3 等因素对子叶再生的影响。观察到DJ 添加物(辣椒幼苗茎叶提取汁液∶卡那霉素= 500∶1) 对不定芽的分化及伸长有明显的促进作用, 比对照分别提高10. 0 %～11. 1 %和90. 5 %～133. 3 %。筛选出高效芽分化培养基为MB+ IAA 1. 0 mg/L + 62BA 5. 0 mg/L + DJ 5 000. 0 mg/L + AgNO3 10. 0 mg/L , 17 个品种平均芽分化率达92. 3 %;高效芽伸长培养基为MB + IAA 1. 0 mg/L + 62BA 5. 0 mg/L + DJ 5 000. 0 mg/ L + AgNO3 10. 0 mg/ L + GA3 2. 0 mg/ L , 17 个品种平均芽伸长率达57. 8 %; 高效生根诱导培养基为MS + IAA 0. 2 mg/ L + NAA 0. 1 mg/ L ,生根率达90 % , 建立了辣椒子叶高效植株再生体系。     

Clonal propagation of Poncirus trifoliate through culture of shoot primordia

Summary

In Poncirus trifoliate, a highly efficient clonal propagation system for the culture of shoot primordia was devised. Shoot primordia were induced at the base of hypocotyl tissue cultured on MS medium supplemented with 44.4 µM BA, 3% sucrose and 0.8% agar. In MS liquid medium (44.4 µM BA, 3% sucrose) on a rotary shaker at two revolutions per minute, shoot primordia of Poncirus grew in size and number. Plant regeneration occurred on MS solid medium. Frequency of regeneration was highest on MS basal medium containing 3% sucrose and 0.8% agar. About 75 shoot buds regenerated from one shoot primordium. Histological observations showed that shoot buds arose from cells in the hypodermal layers of the shoot primordium. The shoot bud developed a vascular system, which became connected to the shoot primordium tissue. Regenerated shoots rooted on 1/2 MS basal medium or 1/2 MS medium supplemented with 0.5 or 5.0 µM IBA. These rooted shoots were acclimatized easily under intermittent mist.     

‘艾西丝’南瓜子叶的离体培养

用‘艾西丝’南瓜子叶作外植体离体培养，成功地建立了一套子叶高频率诱导再生芽的程序。在ＭＳ＋ＢＡ ４．０ｍｇ／Ｌ＋ＩＡＡ０．４ｍｇ／Ｌ的培养基上，以４ｄ苗龄子叶基部切块为外植体，其不定芽的诱导率最高，达５０％，在ＭＳ＋ＢＡ０．２５－０．５ｍｇ／Ｌ的培养基上继代，增殖培养效果较好，在无激素的１／２ＭＳ培养基上最易生根。     

连香树离体快繁初步研究

 连香树为我国珍稀濒危树种, 具有较高的经济价值和观赏价值。本文研究了3年生连香树(Cercidiphyllum japonicum Sieb. et Zucc. ) 带芽茎段的离体培养。筛选出最佳培养基: (1) 腋芽诱导培养基: MS +NAA 0.01 mg·L ^{- 1} ; (2) 丛生芽诱导培养基: MS +BA 1.0 mg·L ^{- 1} ; (3) 丛生芽增殖培养基:MS +BA 2.0 mg·L ^{- 1} + 2,4-D 0.01 mg·L ^{- 1} ; (4) 生根培养基: 1 /2MS + IBA 1.0 mg·L ^{- 1}。     

Fruit set and June drop in Cox's Orange Pippin apple as affected by pollination and treatment with a mixture of gibberellins A4 and A7

Single spray applications of 100 ppm of a mixture of the gibberellins A₄ and A₇ (GA_{4 + 7}) were made on fruiting spurs of the apple cultivar Cox's Orange Pippin to investigate the effect on set, June drop and growth of fruits, as well as on shoot development and flower-bud formation on the bourses. Applications were made from 1 to 50 days after full bloom following partial hand-pollination of flowers, i.e. two stigmas per flower pollinated. In another experiment applications were made from 1 to 20 days after full bloom following complete (five stigmas per flower) or partial (two stigmas per flower) hand-pollination, after open pollination, or on emasculated flowers.GA_{4 + 7} only temporarily increased fruit set after open pollination or after effemination of flowers, and then only after application 1 day after full bloom. GA_{4 + 7} did not affect the very high fruit set after complete or partial hand-pollination. Both latter pollination treatments induced an equally high fruit set.GA_{4 + 7} reduced June drop significantly whenever fruits were left after first drop, except after early applications following open pollination. GA_{4 + 7} was effective in June-drop reduction up to 40 days after full bloom, i.e. until the onset of the June drop.Fruit size was not clearly affected by GA_{4 + 7}. The smaller fruits obtained in some cases after GA treatment could be explained by assuming that maturity was reached by fruits that would have abscised without an exogenous GA_{4 + 7} supply. GA_{4 + 7} also increased seed abortion. Fruit length was increased by GA_{4 + 7} only for applications made up to 20 days after full bloom.GA_{4 + 7} stimulated bourse-shoot development to some extent. Flower-bud formation on the bourses was not clearly affected by GA_{4 + 7}, but was markedly influenced by the presence of fruits.That GA_{4 + 7} reduced June drop so much in spite of a slight promotive effect on bourse-shoot growth and a slight abortive action on seeds suggests that these gibberellins may be specific stimuli for apple-fruit growth after actual fruit set is achieved.