Effects of temperature and plant growth regulators on anthocyanin synthesis and phenylalanine ammonia-lyase activity in chicory (Cichorium intybus L.)

Summary

This study addresses the effects of air temperature and plant growth regulators on anthocyanin synthesis, sugar content and phenylalanine ammonia-lyase (PAL) activity in chicory (Cichorium intybus L.). Anthocyanin in chicory was synthesised at the highest level under 15°/10°C (day/night) temperatures, followed by 20°/15°C, and 25°/20°C; while synthesis was inhibited > 90% at 30°/25°C, resulting in an almost green colour. Sugar contents paralleled anthocyanin development under the same temperatures. The plant growth regulators, abscisic acid (ABA), ethephon and uniconazole all stimulated anthocyanin synthesis, with uniconazole treatment showing the greatest effect. Gibberellic acid (GA₃) inhibited anthocyanin development, while GA₃ in combination with uniconazole alleviated this inhibition.

PAL activity was higher at 15°/10°C or 20°/15°C (day/night) temperatures when plants were treated with ABA, ethephon or GA₃, than at 25°/20°C and 30°/25°C (day/night) temperatures. These results suggest that, under lower temperatures, plant growth regulators may play an important role in anthocyanin synthesis and PAL activity in chicory.     

Factors affecting the response of tulips to gibberellin

Gibberellic acid (GA₃) treatment of forced tulip crops has potential for producing faster growth to anthesis in the glasshouse, for reducing losses due to floral bud blasting, and for reducing the duration of cold storage needed to obtain satisfactory flowers. Using partly and fully cooled direct-forced tulips, cultivar ‘Apeldoorn’, several factors (relevant to the definition of GA₃ treatments) were studied. Experiments confirmed the previously recorded effects of gibberellins in tulips: GA₃ injections reduced the duration of the glasshouse period, enhanced flower survival and flower length, and reduced stem length at flowering.Following bulb storage at temperatures from ?2 to 20°C, GA₃ reduced the glasshouse period by 15–25% and increased flower length, compared to controls, irrespective of storage temperature. Stem length was also reduced by GA₃, this effect being greater following a storage temperature of 5°C or lower. When GA₃ was applied during the period of 17°C-storage which precedes cool storage, or during or after storage at 5°C, it was found that treatments during or at the end of cool storage were more effective in producing the characteristic effects of GA₃ than were pre-cooling applications. In partly cooled bulbs (but not fully cooled ones), the GA₃-induced earliness of flowering was about doubled when GA₃ injections were given repeatedly at 2-week intervals throughout storage. The responses to GA₃ injections were found to be unmodified by early-lifting and heat-treatment (for earlier forcing), by delaying the start of 5°C storage (for later forcing), by glasshouse temperature (16 and 18°C), and by shading treatments; there was little effect of bulb size.     

Growth of Vitis vinifera L. and Vitis aestivalis Michx. as Affected by Temperature

Abstract

Four European (Vitis vinifera L.) winegrape cvs., ‘Semillon’, ‘Pinot Noir,’ ‘Chardonnay’, and ‘Cabernet Sauvignon’, and one American (Vitis aestivalis Michx.) winegrape cv. ‘Cynthiana’, were subjected to three temperature regimes in growth chambers set at 20/15°C, 30/ 25°C, or 40/35°C, for 16/8 hr day/night to determine the influence of temperatures on vine growth and development. In general, the best temperature for shoot and root growth 28 days after temperature treatments was 20/15°C for ‘Semillon’, ‘Cabernet Sauvignon’, and ‘Cynthiana’, and 30/25°C for ‘Pinot Noir’ and ‘Chardonnay’. Although 40/35°C reduced number of leaves, shoots, tendrils, and internodes, total leaf area (LA), and total shoot biomass of all the cultivars, the reduction was more pronounced in ‘Cynthiana’ than in the European cultivars. The average reduction in number of leaves at 40/35°C for the European cultivars was 47%, compared with 92% for ‘Cynthiana’. The two types of grapes adapted differently to high temperature. Shoot growth in the European cultivars continued under high temperature, whereas growth ceased in ‘Cynthiana’. Roots of ‘Cynthiana’, however, were less susceptible to the adverse effect of high temperatures than were the shoots. This study shows that the European cultivars were relatively more tolerant to high temperature than the American cultivar and they have a potential for production of wine in the climate of south central Kansas.     

Substitution of the cold requirement of tulip CV. ‘apeldoorn’ by GA3

To investigate whether GA₃ can substitute for the requirement, 1 mg GA₃ was injected in dry stored bulbs before, during or after the following treatments: (a) 12 weeks at 21°C, (b) 12 weeks at 5°C, (c) 6 weeks at 21°C followed by 6 weeks at 5°C, and (d) 6 weeks at 5°C followed by 6 weeks at 21°C. The bulbs were then planted in light at 15°C. Plants from bulbs previously subjected to (d) flowered earlier than bulbs from treatments (a) and (c) but later than those subjected to (b). Both the GA₃ and the 5°C treatments shortened the time from planting until flowering; however, GA₃ produced shorter plants and induced the formation of parthenocarpic fruits. Reduction of scape length by GA₃ was less when it was given at a later time during treatments (a) and (c) whereas the scape lengths of bulbs subjected to treatments (b) and (d) were hardly affected by the time chosen for GA₃ application.     

Effect of GA3, CCC defoliation and quantum flux density on growth and flowering in Pelargonium × hortorum

In vegetatively propagated Pelargonium × hortorum plants, formation of axillary shoots and initiation of inflorescences and leaves were promoted by an increase in quantum flux density, whereas application of GA₃ had a negative effect. Application of CCC caused an increase in number of axillary shoots and consequently an increase in number of inflorescences and leaves per plant.Dry weight increase was promoted by an increase in quantum flux density, unaffected by GA₃ treatment, but inhibited by CCC treatment. Moreover, continuous removal of the oldest leaves reduced the number of inflorescences, leaves, axillary shoots and dry weight. The changes in inflorescence and leaf initiation could not be definitely correlated to the changes in dry weight increase.     

Influence of temperature on selenium and sulphur accumulation in Brassica oleracea L.

Summary

Selenium (Se) and sulphur (S) accumulation are affected by many factors in plants. To understand how growing temperature affected Se and S uptake and accumulation in Brassica oleracea, plants were grown at three different temperatures: 10°, 20° and 30°C. Plant growth, as reflected in fresh weight (FW) and dry weight (DW), increased with increasing temperature. Se and S accumulation were temperature-dependent and tissue-specific. Se levels increased linearly with increasing temperature in the leaves, and varied from 1.73 – 2.54 mg Se g^–1 DW. Conversely, Se accumulation decreased linearly with increasing temperature in the roots, and varied from 2.17 – 2.87 mg Se g^–1 DW. Growing temperature significantly affected S accumulation in leaves, but not in shoots or in roots. Sulphur levels ranged from 20.83 – 30.98 mg g^–1 DW in leaves, and increased with higher temperatures. Sulphate accumulation was similar to S, except that accumulation decreased at the highest growing temperature. Vegetables that accumulate S can be an efficient means and an effective alternative to deliver Se in human diets. To ensure that optimal levels of Se are attained in plants, without negative effects on plant productivity, factors that affect uptake and accumulation, such as growing temperature, need to be better understood.     

Influence of temperature,soil moisture and CCC on the flowering of Euphorbia fulgens

In the short-day plant Euphorbia fulgens under short-day conditions the flower induction in the shoot apex is delayed more and more nodes are formed beneath the final cyathium, the higher the temperature up to 28°C. The delay of induction is greater with plants growing in a moist soil than in a dry soil. The difference between moist and dry soil is greater, the higher the temperature. There are slight temporal differences in the induction of the lateral shoots in the temperature range between 15°C and 25°C, but the number of nodes formed at the lower paracladia is greater at the higher temperature. The development of the cyathia is enhanced at high temperatures. At temperatures above 28°C induction is prevented. The temperature limit for induction is some degrees higher for plants in dry soil than for those in moist soil. Cycocel causes effects similar to those caused by water deficiency, although the newly formed internodes become shorter.     

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.     

The effect of light,darkness and temperature on micropropagation of the pear rootstock BP10030

There was no effect of irradiance level on surviving percentages of shoot tip explants of the pear rootstock BP10030, but low irradiance stimulated the initial growth of the explant. Irradiance had a strong effect on shoot multiplication. With an increase in photosynthetic photon flux (PPF) from 10 to 80 μmol m^?2s^?1, shoot number and length and shoot fresh and dry weights increased. The greatest number of shoots and the longest ones were obtained with a 16 h photoperiod, while the highest fresh and dry weight of shoots were produced with a 24 h photoperiod. Rooting percentage and the number of roots were markedly promoted under 80 μmolm^?2s^?1 PPF. Photoperiods of 8, 16 and 24 h produced similar effects on rooting percentages and the numbers of roots. Four to seven days of darkness were the optimum for rooting. Rooting percentage and the number of roots increased with increased temperature during darkness between 5 and 25°C. A further increase in dark temperature up to 30°C reduced rooting percentage and root number.     

In vitro morphogenesis and growth of Narcissus in response to temperature

In vitro morphogenesis and growth of tissues of the Narcissus cultivar ‘Lord Nelson’ have been assessed in constant and alternating temperatures. Tissue of leaf-base and scape origin, producing leafy shoots and bulblets on a defined sterile medium, were grown at constant and alternating temperatures of 15, 20, 25 or 30°C and 15–25 or 20–25°C, respectively, in a 16-h daily photoperiod. The number of leaves, leaf length, volume of tissues, fresh weight (but not percentage dry matter), and the number of shoots that would ultimately produce bulbs, were maximal at a constant temperature of 25°C as compared with all other temperature-regimes tested.     

Interaction with salinity of GA3-induced leaf elongation,petiole pithiness and bolting in celery

GA₃ sprayed on celery plants, which received a continuous supply of 0, 0.2, 0.4, 0.6 or 1.0% NaCl solutions to the roots, caused a pronounced increase in leaf elongation.Along with enhanced elongation, GA₃ increased breakdown of parenchymatous tissue in the petiole, but this effect was drastically suppressed in the salt-treated plants. In a similar fashion, the effect of GA₃ on the elongation of the flowering-stem (bolting) was significantly diminished in salt-treated plants. In no case did the salinity treatment totally abolish the bolting-process induced by GA₃.Changing the temperature of the lower part of the root system altered the magnitude of GA₃ effect on bolting. As the temperature was lowered from 30 to 6° C, the ability of GA₃ to cause bolting was greatly reduced.The results are discussed in view of the possible interaction between salinity and the GA₃ effect on petiole elongation, cellular breakdown and bolting.     

Effects of ancymidol and gibberellins A3 and A4+7 on Tulipa gesneriana L. cv. Paul Richter during development in the greenhouse

The influence of soil drench applications of ancymidol (0.5 mg), GA₃ (25 mg), and Ga₄₊₇ (25 mg) was determined on the growth and development of the tulip under greenhouse conditions. Ancymidol applied on greenhouse day 1 or 6 significantly reduced the total length of the scape. Maximum reduction in growth occurred in the first internode, with a declining effect on internodes 2, 3 and 4. GA₄₊₇ applied simultaneously with ancymidol completely reversed the ancymidol effects. GA₃ was relatively ineffective. Compared to control plants, ancymidol reduced the number of cell divisions in the first internode, but not in the fourth internode. Cells of ancymidol treated plants were reduced in length and exhibited greater radial expansion. Ancymidol reduced the fresh weight of the stem and tended to conserve the fresh weight of the mother scales. The effect on the leaves and roots was variable. Ancymidol tended to increase the fresh weight of the daughter bulblets. There was no significant effect of ancymidol or the GA's on floral morphology or the number of days to flower in the greenhouse.     

Effect of stratification-temperature,chemical treatments and seed coat on the growth of peach seedlings cultivar ‘Sharbati’

In order to obtain normal seedlings of peach cultivar ‘Sharbati’ before the commencement of winter, treatments with GA₃, thiourea and kinetin were given to seeds before stratification at 7°C, 10°C or 24°C. The seedlings raised from the treated seeds and after-ripened at 24°C were dwarf. The seedling growth was increased when the treated seeds were stratified at 10°C or 7°C and the stratification period was prolonged from 15 days to 75 days. 10°C stratification-temperature was better than 7°C. The seedling growth was improved when the seed coat was removed before the treatments. With respect to both seed types, 1000 mg/l GA₃ produced the tallest seedlings at all the after-ripening temperatures and during each stratification period. The next best treatment was 100 mg/l kinetin.     

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.     

Flushing and Leaf Growth of Cacao Under Controlled Temperature Conditions

Young clonal cacao trees have been grown for nine months in controlled- environment rooms at 74° F.,80°F. or 86° F. (23·3° C., 26·7° C., or 30·0° C.), or at one of these temperatures during the day and another during the night.

No specific temperature requirements for leaf flushing, which occurred in all the treatments, were found. Flushing was considerably greater at the higher temperatures, partly as a result of the loss of apical dominance, and was especially sensitive to day temperature.

The number of expanded leaves per flush and mean area per leaf increased with a decrease in day or night temperature, as did the duration of the leaves on the trees. The biggest net leaf area increases were made by plants given a day at 80° F. and a night at either 80° F. or 74° F. A night temperature of 86° F. resulted in a rapid turn-over of small unhealthy leaves having a low chlorophyll content.

The gain in total plant dry weight was greatest at a night temperature of 74° F., smallest at a night temperature of 86° F., and the plants which maintained the greatest leaf areas also gained the most dry weight. Leaf dry weight per unit leaf area was greatest at the lowest temperatures, as was the ratio of total plant dry weight to leaf area. The ratio of leaf weight to plant weight showed a small but significant increase with increase in day temperature.     

The physiology of hyacinth bulbs. XI. The effect of gibberellic acid on the growth and flowering of variously chilled bulbs

The effect of gibberellic acid, GA₃, on the growth and flowering of hyacinth cultivars ‘Pink Pearl’, ‘Delft Blue’ and ‘Carnegie’, chilled in a cold room at 5°C or a garden frame for 28, 42 or 81 days, and either rooted or dry, unrooted, was investigated. GA, was applied to the basal plates of the bulbs in a lanolin paste on 10 October 1975.The growth of the inflorescence and leaves of plants originating from dry-chilled bulbs was generally the same as that of those grown from rooted plants. A similar response to GA₃ treatment was observed in all cultivars. Treatment of bulbs with GA₃ decreased the number of days to flowering, stimulated the growth of inflorescences and leaves, and its effect was most pronounced in the plants chilled for shorter periods.     

An analysis of the growth of forced tulips. 1. Changes in plant fresh and dry weights during growth at two temperatures

Changes in the fresh and dry weights of the component parts of plants of tulip cv. ‘Apeldoorn’ were followed in bulbs kept at low and high temperatures (9 and 18°C respectively) from the time of completion of flower differentiation until anthesis.There were marked differences between shoot dry weights at the two temperatures. At 9°C the stem, leaves and flower grew exponentially throughout the whole period, but at 18°C the specific growth rate of the stem and leaves declined throughout the period of the experiment. At 9°C the proportion of total dry weight in shoots and daughter bulbs was higher than at 18°C, and the proportion in the mother bulb was correspondingly smaller.At both temperatures the $\text{fresh weight}\text{dry weight}$ ratios of the mother bulb, shoot and daughter bulbs declined during dry storage, the decline being greater at 9°C. After planting, the ratio for all plant parts increased at 9°C, but scarcely changed at 18°C.These results are discussed in relation to dormancy, to the low-temperature requirement for successful and rapid flowering and to flower quality.     

Nutritional and cultural factors affecting rooting of papaya (Carica papaya L.) in vitro

Summary

Experiments were conducted to optimize nutritional and cultural requirements for initiation and growth of roots on papaya in vitro. Axillary shoots were obtained from plants which had been sub-cultured monthly for two years. Root initiation was enhanced when 1 to 2 mm of stem base was removed and shoots were growing actively before transfer to the rooting medium. Decreasing daylength during incubation from 24 h to 12 h promoted root initiation. Within the day temperature range of 22 to 29°C, optimum rooting occurred at 27°C and higher temperatures produced higher mean root weights per shoot. High concentrations of growth factors and the absence of sucrose in the medium both reduced root initiation, however, varying the concentration of sucrose and removing growth factors affected mean root weight per shoot. All media contained a modified de Fossard et al. (1974) basal medium plus 10 μM IBA.     

Root shoot interactions in passionfruit (Passiflora sp.) under the influence of changing root volumes and soil temperatures

Summary

Passionfruit are grown in the tropics and subtropics where mean monthly soil temperatures at 15 cm range from about 10° to 30°C. The choice of rootstock can also influence production with most industries exploiting either the purple (Passiflora edulis f. edulis) or golden passionfruit (P. edulis tflavicarpa). We examined the relationship between shoot and root growth in purple x golden hybrid E-23 grafted onto golden passionfruit seedlings. Growth was manipulated by varying the volume of the soil available to the roots or temperature of the root zone. Shoot and root growth increased as root zone volume increased from 0.3, 1.4, 4, 12 to 24 1. Shoot weight (W_s) was correlated with root weight (W_R):W_S = 12.697 + 5.272 W_R + 0.195 W_R² (r² = 91%, P<0.001), with the plants allocating a smaller proportion of dry matter to the roots as root weight increased. Differences in shoot growth with pot volume were not due to changes in water or nutrient status. In the temperature experiment, the two critical root zone temperatures at 90% of maximum growth were about 20° and 35° C for vine extension, leaf area, node and leaf production, and 20° and 30°C for flower production. Leaf and stem dry weight were optimal between about 18° and 34°C, while maximum root growth occurred at 38°C. There was a weak relationship between shoot (W_s) and root dry weight (W_R): W_s = ?19.346 + 24.500 W_R ?1.046 W_R² (r² = 53%, .P<0.001). Apparently, variations in shoot growth at different soil temperatures cannot be explained solely by differences in root growth. Reduced growth at 10°C was associated with lower chlorophyll concentration, stomatal conductance and net CO₂ assimilation, but not lower leaf water potential. The concentration of most nutrients were lower at 10°C than at higher temperatures, but none was outside the range which would be expected to restrict growth. There appears to be a co-ordination of shoot and root growth as the soil volume available for root growth increases, whereas root temperature affects the roots and tops differently. The results of the pot volume experiment demonstrate the importance of rootstock vigour in passionfruit breeding. Productivity would be affected in cool subtropical areas with soil <20°C and in tropical areas with soil >30°C.     

Effects of bud scales and gibberellins on dormancy of in vitro cultured Japanese pear leaf buds

Leaf buds of Japanese pear were collected in early June and early November and regarded as summer and winter dormant buds, respectively. Bud explants with and without scales were prepared from each of them, and cultured in vitro for 75 days at 25°C with 14 h photoperiod, on a medium either without growth regulators, or supplied with BA and GAs (GA₃ and GA₄₊₇), singly or in combination.When either BA or GA₄₊₇ was contained in the medium, bud expansion occurred. Thereafter, summer dormant buds grew into shoots in the presence of BA, while winter dormant buds, although they swelled profusely, remained in a rosette. In the presence of BA, GA₄₊₇ markedly stimulated shoot elongation of summer dormant buds, but GA₃ did not. In winter dormant buds, GA₄₊₇ not only failed to stimulate shoot elongation, but also interfered with the BA-induced swelling described above.The presence of bud scales delayed expansion of summer dormant buds, while it had little effect on winter dormant buds. The delaying effect of scales on expansion of summer buds was effectively removed by application of GA₄₊₇ to the medium.