In vitro propagation of ‘Troyer’ citrange from epicotyl segments

Isolated epicotyl, root meristem and root segment tissues of ‘Troyer’ citrange [Poncirus trifoliata (L.) Rat. × Citrus sinensis (L.) Osbeck] were established in continuous culture to compare their regeneration potential. Callus was obtained from these explants on a Murashige—Skoog (MS) medium containing NAA (10 mg l^?1) and BAP (0.1–10 mg l^?1). Formation of shoots from root segments was direct without callus formation on MS medium containing BAP (10 mg l^?1) and NAA (1 mg l^?1). Shoot formation from epicotyl callus occurred on MS medium containing 0.25 mg l^?1 BAP and 0.1 mg l^?1 NAA. Formation of shoots from epicotyl segments occurred on MS medium containing BAP (0.5 mg l^?1) and NAA (0.1–1.0 mg l^?1), while rooting of regenerated shoots occurred in treatments containing 2.0 mg l^?1 NAA alone. This system provides a rapid method for propagation of ‘Troyer’ citrange.     

Effect of gibberellic acid (GA3) on elongation and rooting of ‘St. Julien A’ rootstock in vitro

‘St. Julien A’ (Prunus instititia L.) rootstock was induced to proliferate shoots on a modified half-strength Murashige and Skoog (MS) medium. Cultures treated with 12.5 mg l^?1 gibberellic acid (GA₃) produced elongated shoots suitable for rooting. Elongated shoots were placed in media with indolebutyric acid (IBA) or indole-3-acetic acid (IAA) with or without a 16-day dark incubation. Light (16-h photoperiod) inhibited rooting. IAA (4 mg l^?1) was ineffective in promoting rooting. Rooting was best when shoots were incubated in the dark with IBA (4 mg l^?1). GA₃ was deleterious to shoots, causing chlorosis and apical die-back. Light regime interacted with auxin treatments in affecting shoot condition. Shoot condition was better on shoots treated with IBA and dark-incubated; while those treated with IAA were better when light-incubated.     

Effect of GA3, Planofix (NAA) and Ethrel on granulation and fruit quality in ‘Kaula’ mandarin

The effect of GA₃ 15 mg l^?1, Planofix (NAA = 1-naphthalene acetic acid) 300 mg l^?1 and Ethrel 250 mg l^?1 on granulation and fruit quality in ‘Kaula’ mandarin (Citrus recticulata Blanco) was studied during 1975–1976. Three sprays of Planofix reduced the incidence of granulation to 30.7% from 62.7% in control. Three sprays of GA₃ were almost equally effective (31.3% granulation). These treatments also improved the fruit quality and gave the highest fruit weight, pulp percentage, juice, T.S.S., reducing and non-reducing sugars and ascorbic acid, and the lowest acidity, peel and rag. In both these treatments (3 sprays of GA₃ or Planofix) the T.S.S. was 9.3% (8.1% in control). The application of 3 sprays of Planofix 300 mg l^?1 or GA₃ 15 mg l^?1 is, therefore, considered to be successful in reducing the granulation in this cultivar of mandarin.     

Use of 6-benzylamino purine and Promalin for improved canopy development in selected apple cultivars

Foliar sprays of Promalin (gibberellins A_{4 + 7} + 6-benzylamino purine) applied to 1-year-old apple (Malus domestica Borkh.) trees at the 3–5-cm growth stage significantly increased lateral branching in 5 of 9 cultivars tested. Branching response ranged from 0% (‘Winter Banana’) to 131% (‘Starkrimson Delicious’) of the untreated controls. Total shoot growth was not consistently increased by 6-benzylamino purine or Promalin in tests over 3 years on spur and non-spur 1- and 2-year-old apple trees. Sprays of 50–300 mg l⁻¹ Promalin were ineffective for increased branch development. Sprays of 300–500 mg l⁻¹ increased total shoot numbers and reduced average shoot length. Sprays applied prior to new terminal growth in spring were ineffective. Treatment during periods of active shoot growth were generally effective, but periods of stress may have reduced response. Sprays were more effective for inducing lateral shoot formation than dormant heading or delayed dormant heading (pruning) (10 days after full bloom) in ‘Criterion Golden Delicious’. No difference in branching response was observed between BA and Promalin. Addition of a spray adjuvant (Buffer-X) did not affect branching response. Repeat annual single sprays of Promalin applied to dormant pruned trees were generally less effective for stimulating lateral branching than a single application in a given year. Phytotoxicity was associated with Promalin sprays at 300–500 mg l⁻¹ on ‘Delicious’.     

In vitro propagation of garlic by shoot proliferation

Shoot buds (5–8 mm long), excised from dormant cloves of the New Zealand commercial garlic (Allium sativum L.) and a virus-free French cultivar ‘Rose-de-Kakylis’, proliferated both axillary and adventitious shoots on B-5 basal medium supplemented with 0.5 mg l^?1 isopentenyladenine (2-ip) and 0.1 mg l^?1 naphthaleneacetic acid (NAA). An 8-fold increase in shoot number occurred every 6 weeks. Shoots were readily rooted in B-5 + 0.01 mg l^?1 2-ip + 0.2 mg l^?1 NAA and transferred to pots, where about 70% of the shoots formed established plants. The plants raised by this shoot-proliferation method retained the diploid condition of the parents.     

Shedding of the upper parts of grapevine shoots

Shedding of the upper parts of unlignified grapevine (Vitis vinifera L.) canes is frequent during autumn. Stress conditions during the growing-season lead to similar shedding of shoot tips. The separation process occurs above a node in the boundary area between the distal part of the diaphragm and the pith.Ethephon (2-chloroethyl-phosphonic acid) sprays, at 750 or 1500 mg l^?1, induced separation of the shoot tips of ‘Perlette’ and ‘Queen of the Vineyards’. Ethylene (C₂H₄) 200 vpm and ethephon at 10, 100 and 1000 mg l^?1 enhanced separation in shoot explants, whereas 2,4,5-TP (2,4,5-trichlorophenoxy-propionic acid) at concentrations above 1 mg l^?1 arrested it.This phenomenon may be regarded as a shoot abscission process which may represent adaptation of self-pruning of the grapevine.     

Rapid propagation of Cucurbita pepo L. by culture of meristem tips

A tissue culture technique has been developed for the rapid multiplication of pumpkin (Cucurbita pepo L.) clones. Meristem-tips from seedlings of cultivar ‘Cinderella’ were grown initially on MS medium containing 2.56 mg l^?1 Kinetin and 8 mg l^?1 IAA, and then transferred to experimental media. Maximum shoot proliferation occurred on MS medium containing 1 mg l^?1 BA and no auxin. Cultures were rooted after 2–3 weeks on MS medium containing 8 mg l^?1 IAA and no cytokinin.     

Influence of growth regulators on setting,retention and weight of fruits in two cultivars of litchi

Investigations were undertaken to explore the possibility of improving setting, retention and weight of fruits in ‘Early Seedless’ and ‘Calcuttia’ cultivars of lichi (Litchi chinensis) by means of growth regulators. Indole acetic acid (IAA) at 20, 40 and 80 mg l^?1, 2,4-dichlorophenoxy acetic acid (2,4-D) at 2,4 and 8 mg l^?1 and gibberellic acid (GA₃) at 50, 100 and 150 mg l^?1 were sprayed on panicles in the first fortnight of April, when 50–100% flowers had opened. All 3 growth regulators caused a favourable effect on fruit setting, fruit retention and weight of individual fruits, but IAA at 20 mg l^?1 proved the best for enhancing setting, GA₃ at 50 mg l^?1 for increasing retention and GA₃ at 100 mg l^?1 for improving fruit weight. IAA and GA₃ should, therefore, be used in combination. Between the 2 cultivars tested, ‘Calcuttia’ proved superior to ‘Early Seedless’ in fruit setting, fruit retention and weight of individual fruits.     

In vitro somatic embryogenesis from Mangifera indica L. callus

The nucellus and globular adventitious proembryos were removed from 2-month-old fruits of mango (Mangifera indica L.) cultivars ‘Ono’ and ‘Chino’, and were cultured on sterile, solid Murashige and Skoog (MS) medium that had been modified as follows: half-strength major salts and chelated iron; 20% (v/v) coconut water (CW); 6% sucrose; 100 mg l^?1 ascorbic acid and 400 mg l^?1 glutamine. Embryogenic explants were sub-cultured after 4–6 weeks in liquid modified MS medium containing 2 mg l^?1 2,4-dichlorophenoxyacetic acid (2,4-D) instead of CW. Rapidly growing cultures were established and were sub-cultured monthly. Somatic embryogenesis was induced following sub-culture from MS medium with 2,4-D to MS without growth regulators and with or without activated charcoal (0.5%). Germination of somatic embryos appeared to be enhanced by 1 mg l^?1 benzyladenine (BA); however, most of the germinating embryos became embryogenic.     

Vegetative growth and nutritional status as influenced by auxins and gibberellic acid,and their effect on fruit yield in lemon

Application of 2,4-D and 2,4,5-T at concentrations ranging from 5 to 20 mg l^?1 to 5-year-old ‘Pant Lemon-1’ (Citrus limon Burm) trees reduced the vegetative growth in terms of height, spread, shoot length, number and size of the leaves in the autumn flush. Various NAA treatments (5–20 mg l^?1), however, enhanced growth, but not to the extent that was observed after GA₃ treatments. Application of GA₃ at 10–40 mg l^?1 significantly enhanced all aspects of growth, and the effects were most pronounced at 20 and 40 mg l^?1. Nutritional status of the leaves showed a slight variation in relation to vegetative growth under various treatments.Some 2,4-D- and 2,4,5-T-treatments increased the fruit yield over the control, which could suggest mobilization of foods even at the expense of reduced vegetative growth. On the other hand, NAA, particularly at 10 mg l^?1, increased both vegetative growth and yield, suggesting that the transport of the photosynthates from the leaves to the fruits was not at the expense of new growth extension. Due to excessive growth enhancement under higher concentrations of GA₃ (20 and 40 mg l^?1), comparatively fewer nutrients were translocated to the fruit “sinks”, thereby resulting in a non-significant decrease in yield.     

Adventitious shoot formation from sections of sweet potato grown in vitro

Sweet potato (Ipomoea batatas Lam.) root sections were obtained from the cultivars ‘Centennial’, ‘Redmar’ and ‘Jewel’ with a No. 6 cork borer. These sections were cut into 2–3-mm discs and explanted on to modified Murashige and Skoog (MS) medium consisting of MS high mineral salts, myo-inositol (100 mg l^?1), Staba vitamins, 6-benzyl-aminopurine (2.0 mg l^?1), naphthaleneacetic acid (0.1 mg l^?1), sucrose (30 g l^?1) and agar (10 g l^?1). Root discs from internal regions of the tuberous roots gave rise to calli and meristematic bud-like centers (MBLC's). A small percentage of ‘Centennial’ MBLC's burst open to reveal plantlets which grew and rooted well on the medium. Some of the ‘Jewel’ MBLC's contained only roots, while those of ‘Redmar’ did not differentiate. MBLC-formation occurred most often on discs taken from fresh (unstored) roots of ‘Centennial’. Petiole sections taken from in vitro-cultured plants of all 3 cultivars developed plants quite readily on the medium. Shoots of all 3 cultivars grew rapidly, to yield whole rooted plants which could easily be moved to soil and grown in the greenhouse and field.     

The influence of wax emulsion,morphactin and gibberellic acid on the storage behaviour of indian gooseberry fruits

Qualities of Indian gooseberry fruits (Phyllanthus emblica L.) were determined after dip-treatment with wax emulsion (WE) with or without morphactin (Mor) and gibberellic acid (GA₃). Dip-treatments with 100–500 mg l^?1 Mor reduced marketability by inducing browning and high weight loss, but loss in ascorbic acid was checked and phenols increased. 10 mg l^?1 Mor maintained marketability at par with control, effectively controlled loss in ascorbic acid, and increased acidity and reducing sugars. GA₃, although failing to control the loss of ascorbic acid, was effective in checking browning and thereby increased the market value of fruits as compared with controls and Mor-treated fruits.WE with or without Mor (10 mg l^?1) controlled browning, accumulation of phenols and losses in weight and moisture as compared with 10 mg l^?1 Mor, 100 mg l^?1 GA₃, or control, but could not retain ascorbic acid in comparison to 10 mg l^?1 Mor-treated fruits. Marketability of fruits having had treatment with either WE or GA₃ was the same. Fruits having had combined treatment with WE and 10 mg l^?1 Mor had maximum marketability. Minimum marketability was observed in fruits subjected to a combined treatment of WE + 100 mg l^?1 GA₃ due to maximum infection with Aspergillus spp. and Penicillium spp.     

Effects of ozone and sulfur dioxide on grapevines

Greenhouse-grown ‘Ives’ and ‘Delaware’ grapevines (Vitis labruscana, Bailey) were fumigated for 4-hours with ozone (O₃) and/or sulfur dioxide (SO₂) at 0.40 and 0.80 mg l^?1. Fumigations were performed in a plexiglass chamber situated within a controlled environment walk-in growth chamber. When applied separately, both gases induced characteristic foliar injury. ‘Ives’ grapevines were much more sensitive to $\text{O}{}_3\text{SO}{}_2$ fumigations than were ‘Delaware’ grapevines. Within each cultivar, leaf necrosis and shoot growth reduction were greatest following fumigation with 0.80 mg l^?1 O₃ plus 0.80 mg l^?1 SO₂. Leaf abscission occurred only on ‘Ives’ and was related to foliar necrosis. Shoot growth following fumigation was less on vines having most foliar necrosis. Yet, ‘Delaware’ vines showing less than 1% leaf area necrosis still had significant reductions in shoot growth. All O₃ and SO₂ fumigations resulted in stomatal opening.     

Cost-effective tissue culture media for large-scale propagation of three commercial banana (Musa spp.) varieties

Cost-effective tissue culture protocols have been established for the commercial multiplication of three banana varieties, ‘Rasthali’ (AAB – Silk), ‘Grand Naine’ (AAA – Cavendish), and ‘Udhayam’ (ABB – Pisang Awak). Reverse osmosis water and 3% (w/v) table sugar were used as the low-cost water and carbon source, respectively. Six different gelling agent treatments were tested: sago alone (T1), Isabgol alone (T2), sago + agar (T3), Isabgol + agar (T4), sago + Isabgol (T5), and agar alone as a control (T6). Full-strength Murashige and Skoog (MS) medium supplemented with 3 mg l^–1 6-benzylaminopurine (BAP) and 1 mg l^–1 indole-3-acetic acid (IAA) were used for culture initiation and subculturing. Rooting was accomplished on low-cost MS medium containing 1.0 mg l^–1 α-napthaleneacetic acid (NAA), 1.0 mg l^–1 indole-3-butyric acid (IBA), and 250 mg l^–1 activated charcoal. Statistical analysis indicated that sago + Isabgol (T5) produced the maximum number of shoots (10 per explant) in ‘Udhayam’ and ‘Rasthali’, while sago alone (T1) produced the maximum number of shoots (6 per explant) in ‘Grand Naine’. The genetic stability of tissue-cultured banana plantlets produced using these low-cost substitutes was assessed using inter-simple sequence repeat (ISSR) markers. The results indicated that the ISSR profiles of the five treatments and the control (T6) were similar, indicating genetic stability using these cost-effective tissue culture protocols. Reductions in cost over the control (l^–1 of MS medium) ranged from 65% to 86%, while the per plant production cost was reduced by 12.5%–20.0%. Adoption of these treatments (T1–T5) as low-cost tissue culture protocols for in vitro propagation would reduce production costs significantly, leading to an expansion of the area planted with tissue-cultured banana, thereby increasing productivity.     

Gibberellic acid soak treatments for fully-cooled tulips

In attempts to reduce the glasshouse period of fully-cooled 5°C-forced tulips, ‘Apeldoorn’ bulbs were soaked before planting in aerated and non-aerated gibberellic acid (GA₃) solutions for 2–48 h. A 48-h treatment with 250–500 mg l^?1 GA₃ was the most effective, giving a glasshouse period 7–11 days shorter than for untreated bulbs. Soaks for 24 and 48 h caused root emergence, and 48-h soaks caused perianth segment splitting in one experiment. Aerated or non-aerated GA₃ solutions gave similar results. Soaking in water alone gave a smaller increase in earliness. In general, a shortened glasshouse period was associated with shorter whole stem and last internode lengths. In GA₃ treatments, flower losses were lower than for distilled water treated and untreated bulbs. A practical treatment would be a non-aerated soak for 24 h with between 250 and 500 mg l^?1 GA₃.     

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.     

Responses of day-neutral,June-bearing and everbearing strawberry cultiv ars to gibberellic acid and phthalimide treatments

Field grown day-neutral, June-bearing and everbearing strawberry cultivars responded similarly to GA₃ in most cases. GA₃ stimulated daughter-plant production in ‘Hecker’ (DN) and suppressed it in ‘Guardian’ (June). Fifty mg l^?1 GA₃ increased initial runner production of all cultivars, while both 50 and 100 mg l^?1 GA₃ increased fruit yield the year following treatment. In greenhouse studies, GA₃ initially increased leaf number, petiole length and runner production, but the effects diminished with time. Phthalimide at 1000 mg l^?1 was most effective in increasing leaf number.     

Rapid seedlings regeneration from seeds and vegetative propagation with sucker and rhizome of Eremospatha macrocarpa (Mann & Wendl.) Wendl and Laccosperma secundiflorum (P. Beauv.) Kuntze

To develop efficient seedling production methods for Laccosperma secundiflorum and Eremospatha macrocarpa, a study was conducted to examine regeneration using offsets combined with several physical and chemical treatments of seeds. Offsets categorized into small, medium and large diameters, were planted in three conditions: shaded and open nursery, and greenhouse. We tested sucker from E. macrocarpa, and sucker and rhizome from L. secundiflorum. For both species, high viability percentage (ranging from 55% to 100%) were observed for small and medium suckers planted in shaded nursery and greenhouse, against less than 49% for sucker planted in open nursery. The mean seedling emergence times were estimated to 84, 77 and 75 days after planting (DAP) for small, medium and large sucker of L. secundiflorum, respectively under open nursery condition, and 76, 75, 95 DAP for small, medium and large suckers of the same species, respectively in shaded condition. Greenhouse has a significant positive effect on E. macrocarpa seedlings emergence time. For this species, the mean seedling emergence times were estimated to 43 DAP for small sucker and 76, 93 DAP for medium and large suckers. No seedling was obtained from rhizome planted in all the growing conditions tested. Concerning seed dormancy breaking, germination percentages and rates were determined for 13 treatments. The best treatments were pre-soaking unscarified seeds for 4 days in 1.01 g l⁻¹ and 0.10 g l⁻¹ KNO₃, with 79% and 68% of germination, respectively and in 3.46 × 10⁻³ g l⁻¹ GA₃ for 68% of germination. These methods are suggested to improve germination of L. secundiflorum seeds. Successful and recommended methods for E. macrocarpa are pre-soaking scarified seeds in 3.46 × 10⁻³ g l⁻¹ and 3.46 × 10⁻⁴ g l⁻¹ GA₃, 96% and 94% of germination, respectively. Dormancy, probably a combination of mechanical and chemical dormancy, is present in the two species.     

Chemical composition of French and Polish cloudy apple juices

Summary

Cloudy juices from six apple cultivars from Poland (‘Ariwa’, ‘Gold Milenium’, ‘Florina’, ‘Melfree’, ‘Novamac’, and ‘Rajka’) and four French cultivars (‘Ariane’, ‘Chanteline’, ‘Judeline’, and ‘Judor’) were produced and chemically characterised. The analyses encompassed 23 chemical parameters and phenolics profiles. The most important parameter, differentiating cloudy juice from clear juice, was turbidity. Cloudy juices were characterised by having an average total turbidity of 1,210 Nephelometric Turbidity Units (NTU) and a stability of turbidity of 42%. Some of the results deviated from the accepted ranges given in reference values for apple juices in the Code of Practice of the European Fruit Juice Association. This occurred in the cases of simple sugars and saccharose contents of the Polish apple juices (e.g., up to 56.9 mg l^–1 of saccharose vs. a maximum value of 30 mg l^?1), and for some mineral compounds in the French apple juices (e.g., sodium values up to 10 mg l^?1). Large variations were found in case of important healthconferring components. Water-soluble pectin contents varied from 205 mg l^?1 for ‘Chanteline’, to 1,289 mg l^?1 for ‘Gold Milenium’; while, in the case of phenolic compounds, the range was from 85.7 mg l^?1 for ‘Novamac’, to 524.8 mg l^?1 for ‘Melfree’.     

The effect of sucrose,silver thiosulphate and 8-hydroxyquinoline citrate on the quality of Lilium inflorescences cut at the bud stage and stored at low temperature

A continuous supply of sucrose together with 8-hydroxyquinoline citrate to cut Lilium Asiatic hybrid ‘Prima’ inflorescences resulted in buds opening satisfactorily and increased their longevity. The best results were obtained using 30 g l^?1 sucrose. Cut Lilium inflorescences could be stored at 1°C for 4 weeks without a great loss in potential vase-life and decorative value when the inflorescences were pre-treated with silver thiosulphate + 100 g l^?1 sucrose for 24 h before cold storage, kept in a cold room in a solution containing 50 mg l^?1 silver nitrate, and after cold storage kept in a solution containing 30 g l^?1 sucrose and 200 mg l^?1 8-hydroxyquinoline citrate. Such treatment greatly improved bud opening, increased the diameters of individual flowers and prolonged their life.