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1.
One-year-old scale and stem bulblets of Lilium longiflorum Thunb. ‘Nellie White’ (Easter lily) were grown under constant and variable growth chamber conditions and greenhouse conditions to compare growth and development and bulb production. Eight temperatures regimes were established using the following: six growth chambers set to provide day/night temperature regimes of 30/26, 26/22, 22/18, 18/14, 14/10 and 10/6 °C; a seventh growth chamber (VAR) programmed to begin at 22/18 °C, then decline in three 4–5 week steps to 10/6 °C, and subsequently increase in three 4–5 week steps to 22/18 °C to simulate seasonal field temperatures in the coastal bulb production area of northern California and southern Oregon; and a double layer polyethylene greenhouse (GH) set to begin cooling at 22 °C and heating at 18 °C. Ten percent of the scale bulblets and 35% of the stem bulblets failed to develop shoots (“no-shows”). “No-shows” increased with increasing temperature with a significant number starting at 18/14 °C. The moderately high GH temperature also induced “no-shows”. Maximum basal bulb (the main planted bulb) weight occurred at 26/22 °C for both bulblet types. Scale bulblets not only produced heavier basal bulbs with a larger circumference than stem bulblets, but also produced heavier stem bulbs. Stem bulb formation and production was maximized in the range of 18/14–26/22 °C and in the GH for scale bulblets. Stem bulb production from stem bulblets did not differ from zero. Scale bulblets produced more basal and stem roots than the stem bulblets at the end of the early growth period, but there was no significant difference at the end of the study. Root fresh weight was greatest in the range of 14/10–18/14 °C and declined at higher or lower temperatures. The VAR and GH treatments had similar root weights to those at 18/14 °C. Shoot length was maximized at 22/18 °C for stem bulblets and in the GH and at 22/18 °C for scale bulblets. Stem plus leaf (shoot) fresh weight was not statistically different between bulblet types with the exception of an increased weight for stem bulblets grown at 22/18 °C. Scale bulblets in the GH had greater stem plus leaf weights than scale bulblets in the other temperature regimes. Shoot leaf number was highest in stem bulblets at 22/18 °C and in the GH. In these two temperature treatments, more leaves were produced by stem bulblets than scale bulblets. In all other treatments, there was no significant difference in leaf number. Bulblet type had no effect on number of flowers produced. Flower number was maximum in the range 10/6–22/18 °C, decreased at 26/22 °C and in the GH, and was absent at 30/26 °C. For bulb production, reduced flowering is desired since flowers are generally removed during the outdoor bulb production period. Meristem abortion, which also causes a desirable reduction in flowers, was greater in scale bulblets. It occurred at 26/22 °C and was greater at 30/26 °C. Scale bulbs produced the largest main bulbs, with a maximum yield at 26/22 °C.  相似文献   

2.
One-year-old scale bulblets of Lilium longiflorum Thunb. ‘Nellie White’ (Easter lily) were grown under a combination of six constant day/night temperature regimes and five N–P–K nutrient treatments under short days for 107 d (growing period 1 or GP-1) to compare the effects on growth and development and bulb production. Results during GP-1 were as follows: failure of bulblets to produce a shoot (“no-shows”) was found at high temperatures (30/26 and 26/22 °C) and not influenced by the nutrient treatments. Flower bud abortion was observed in the minus-N, minus-P, and minus-N–P–K treatments at high temperatures (30/26 or 26/22 °C), but not observed at any temperatures in the complete and minus-K treatments. The loss of bulb fresh weight in minus-N treated bulblets was less than in the other treatments resulting in less root and shoot growth in the minus-N treatment. At the intermediate temperatures where growth was highest, omission of N, P, K, or all three resulted in losses in stem bulb fresh weight, stem plus leaf fresh weight, number of flowers, and stem root fresh weight. Omission of N, P, or all three nutrients resulted in lowest basal root fresh weight. Bulb N and K concentrations were lowest in plants grown with complete nutrient solution at the two coldest temperature regimes (14/10 and 10/6 °C). Bulb P concentration was lowest at the three coldest (18/14, 14/10 and 10/6 °C) and the warmest (30/26 °C) temperature regimes. Stem length was shorter when P was omitted. Omission of any of the three nutrients resulted in lower concentrations of the other nutrients. The one exception was where low K did not affect N concentration. In the second phase of the experiment, plants grown at 18/14 °C and irrigated with the complete nutrient solution for 107 d (GP-1) were continued at this day/night temperature regime and five N–P–K nutrient treatments for another 89 d under long days (growing period 2 or GP-2). Results during GP-2 were as follows. Basal bulb yield was not impacted by omission of N, P, or K, or all three. Of all growth measurements, only stem plus leaf fresh weight was lower and only when all three nutrients (minus-N–P–K) were omitted. At the end of GP-2, basal bulb concentrations of N and P did not differ from the concentrations in bulbs at the beginning of GP-1; however, K concentration was lower at the end of GP-2. Omission of N or P further resulted in lower bulb K concentration, suggesting that a moderate supply of N, P, and K be applied during GP-2 since an additional year of bulb production is needed to produce forcing-sized bulbs.  相似文献   

3.
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4.
The plants of two onion cultivars Sturon and Stuttgarter were raised from sets and placed in a growth room at 12 °C, a light flux density of 120 μmol m−2 s−1 and a 16 h photoperiod. Cultivar Stuttgarter took 195 days to initiate, whereas time for initiation in cv. Sturon was 201 days. After initiation the plants were transferred to wide range of photo-thermal regimes consisting of six set point temperatures (6, 10, 14, 18, 22 and 26 °C) and four photoperiods (8, 11, 14 and 17 h day−1). An overall mean temperature for all developmental stages under each photo thermal combination was 12.2, 12.4, 15.9, 17.8, 23 and 24.4 °C. Time to inflorescence appearance, spathe opening and floret opening decreased linearly as temperature and photoperiod increased. At low to mild temperatures (12.2–17.8 °C), longer photoperiod enhanced florets per umbel, whereas at higher temperatures (23–24.4 °C), the floret number declined with lengthening photoperiods. As the photoperiod extension in each temperature advanced inflorescence appearance, spathe opening and floret opening and this would be beneficial in a programme to accelerate seed production in onion.  相似文献   

5.
The influence of bulb maturity at bulb harvest on growth and flowering response of Ornithogalum thyrsoides Jacq. ‘Chesapeake Starlight’ was investigated. Experiments were designed to determine if bulb maturity can be induced by bulb storage temperatures and whether bulb maturity can be evaluated by flowering responses. Bulbs with all senesced leaves at harvest were considered “mature” or with emerging young leaves and re-growing young roots were considered “immature”. Bulbs were potted after 0, 3, and 6 weeks of 30 °C or 2 weeks of 10 °C given either in the middle or at the end of 6 weeks of 30 °C. Mature bulbs, as compared to immature bulbs, took longer for leaves to emerge when control bulbs that did not receive any temperature treatment after harvest were planted upon harvest. Leaf emergence of the immature bulbs was significantly earlier than that of the mature bulbs. Mature bulbs which received 30 °C for 3 weeks (30 °C/3 week) flowered 31 days faster than immature bulbs and all bulbs flowered. Leaf emergence and flowering of mature and immature bulbs that received 30 °C/6 weeks or 2 weeks of 10 °C in the middle of 6 weeks of 30 °C (30 °C/2 weeks–10 °C/2 week–30 °C/3 weeks) did not differ from each other. Maturity can be induced by storing immature bulbs at 30 °C/6 weeks. Maturity, as evaluated by flowering percentage and days from leaf emergence to flowering, can be induced in O. thyrsoides. Immature bulbs can, therefore, be harvested for later forcing as long as bulbs are treated with 30 °C/6 weeks. It is proposed that maturity can be correlated with the speed of flowering and bulbs can be harvested at immature physiological state for forcing. Postharvest high-temperature treatment can be used to force immature bulbs that were harvested before the senescence of the leaves.  相似文献   

6.
Linaria maroccana Hook. f. Ann., ‘Lace Violet’, Lupinus hartwegii ssp. cruikshankii Lindl. ‘Sunrise’ and Papaver nudicaule L. ‘Meadow Pastels’ seeds were directly sown into 105 cell plug trays and received either ambient light or supplemental high intensity discharge (HID) lighting. For each species, a 2 × 3 × 3 factorial was used with two light intensities during propagation, three transplant stages, and three night temperatures. Seedlings were transplanted at the appearance of 2–3, 5–6, or 8–9 true leaves. Transplanted Linaria and Papaver seedlings were placed at 5/11, 10/16, or 15/21 ± 1 °C night/day temperatures and Lupinus seedlings were placed at 15/24, 18/25, or 20/26 ± 2 °C night/day temperatures. For this study, the optimum production temperature for Linaria was 10/16 °C as the cut stems produced at 15/21 °C were unmarketable and production time was excessively long at 5/11 °C. At 10/16 °C, Linaria seedlings should be transplanted at the 2–3 leaf stage to maximize stem number, stem length and profitability. For Lupinus the optimum temperature was 15/24 °C due to long stems and high profitability per plant. Lupinus seedlings should be transplanted at the 2–3 leaf stage when grown at 15/24 °C to obtain the longest and thickest stems; however, $/m2 week was higher for plants transplanted at the 8–9 leaf stage due to less time in finishing production space. For Papaver, the 15/21 °C temperature was optimal as that temperature produced the longest stems in the shortest duration, resulting in the highest $/m2 week. At 15/21 °C Papaver plants should be transplanted at the 2–3 leaf stage. Supplemental HID lighting had no effect on any of the species.  相似文献   

7.
Red color plays a very important role when wax apple fruits are purchased. Temperature is one of the key factors among those influencing red color development. We evaluated the effects of temperature on color formation and other quality characteristics of ‘Pink’ wax apple fruit discs by using constant, slow-increase, fast-increase, transient shifting to high temperature, shifting to high temperature for different length of time and different day/night temperature regimes. The results show temperature has pronounced effects on quality attributes of wax apple fruit discs. Anthocyanin and total soluble solid (TSS) were greatest in the 20 °C treated discs under constant temperatures. In the slow-increase and fast-increase treatments, quality attributes in disc were better in treatments with a final temperature of 25 °C than of 30 °C. The concentration of soluble sugars (SS), starch, total phenolic compounds (TPC), free amino acids (FAA) and soluble protein (SP) all decreased with increasing temperature. Transient shifting to high temperature of 30 °C for 1-day had no effect on pigmentation but treatment periods from 3- to 5-days had a substantial adverse effect. At 30 °C for 5-days, exposed discs had the lightest weight and shortest diameter as well. Both SS and TPC decreased in the 3- and 5-day treatments. When temperature was shifted from 20 to 30 °C for 2 to 11 days, the widest and heaviest discs were found in the 5-day treatment. Anthocyanin and TSS concentration decreased following increased length of exposure to high temperature. Pigmentation of discs exposed to high temperature treatment was worse than in uncultured controls. Both protein and FAA concentrations decreased after culture. Among the 5 different day/night temperature combinations, discs under 25/20 °C had the highest anthocyanin and TSS concentrations, while those under 30/15 °C had the worst.  相似文献   

8.
High temperatures are known to reduce fruit size and fruit weight in strawberry, but cultivar differences in the response to high temperature stress during the reproductive stage up to the second inflorescence have not been sufficiently reported. We examined the effect of two day/night temperature regimes on fruit set and fruit growth in two cultivars, ‘Nyoho’ and ‘Toyonoka’. A high day/night temperature of 30/25 °C reduced the number of inflorescences, flowers, and fruits in both cultivars compared with plants grown at 23/18 °C. The percentage of fruit set in ‘Nyoho’ was not significantly different between the two temperature treatments, while that in ‘Toyonoka’ was much lower at 30/25 °C than at 23/18 °C. Days to ripening was shorter at 30/25 °C than at 23/18 °C, and no cultivar differences were observed. Fresh weight of primary, secondary, and tertiary fruits was greater at 23/18 °C than at 30/25 °C in both cultivars, and no cultivar differences were observed, except in tertiary fruits. The diameter of fruits from all positions was also reduced at 30/25 °C in both cultivars. Relative growth rates of fruits showed two peaks in both cultivars and in both temperature treatments. Both peaks appeared earlier at 30/25 °C than at 23/18 °C. Percentage of fruit set at 30/25 °C in the second inflorescence was also significantly lower in ‘Toyonoka’ than in ‘Nyoho’. These results indicate that high temperature stress negatively affects the reproductive process in strawberry and that plant response to high temperature stress is cultivar-related in such responses.  相似文献   

9.
The experiment was conducted at the experimental area of the School of Plant Sciences, University of Reading during 1996. The planting material comprised of sets (graded to 22.5 mm diameter) of two cultivars, Hygro and Delta. The sets were stored at 5 °C for nine chilling durations, between 10 and 90 days. A control treatment (sets stored at room temperature of 20 °C for days) was also included in the experiment for comparison. Sets of both cultivars treated for 90 days at 5 °C, produced nearly seven times more bolters than those treated for 20 days. Cool temperature treatment for 10 days was too short to induce bolting. Number of florets and percentage of seed bearing florets per umbel increased with lengthening cold durations and this resulted in higher seed yield per umbel. Mean bulb weight per plant was found to increase with shortening the period of low temperature treatment. For bulb crop, storage of sets at 20 °C for 90 days appears to be optimum, as it checked bolting and increased average bulb weight and bulb yields m−2 in both cultivars.  相似文献   

10.
Reducing energy use in greenhouses contributes to the profitability of horticulture. Important energy savings can be realized through the use of temperature integration. However, such a greenhouse heating strategy is only acceptable for commercial purposes if there are no adverse effects on plant growth and quality. During this 3-month study, Hedera helix ‘Green Ripple’ and H. helix ‘Shamrock’ were subjected to a day/night temperature regime of 20/20 °C (control) and two treatments with temperature integration over 24 h and 4 d, respectively, based on a DIF of 13.5 °C, maintaining the average temperature at the same level of the control. Temperature treatments resulted in a promotion of stem elongation. After 3 months, shoot length rose up to maximum 37.3% when temperature integration was applied. However, temperature integration reduced total dry weight and particularly root dry weight was negatively affected. In addition, assessments of relative growth rate, shoot extension rate, specific leaf area, total leaf area and pigment concentrations were performed and it was concluded that dynamic temperature regimes with longer integration periods support commercial production of English ivy.  相似文献   

11.
This study aimed to compare the interaction between light quality and alternating day (DT) and night temperature (NT) under two different daily light integrals (DLI) on morphology of a wild type (wt) and a phytochrome B deficient mutant (lh) of cucumber (Cucumis sativus L.). Different light qualities were established by light quality selective plastic films. Plants were grown for 18 days (lh) or 19 days (wt) under DT/NT regimes of 25/19 °C (positive DIF), 22/22 °C and 19/25 °C (negative DIF) (12-h thermoperiod) in combination with plastic films establishing a low (0.75, LRFR) and high red (R)/far-red (FR) ratio (1.62, HRFR) and a control (R/FR of 1.11). Stem, hypocotyl and internode elongation in the wt were more affected by DIF under LRFR than HRFR. In general, length was reduced 45–50% under HRFR compared to the control, while the reduction by negative DIF was 38% on average. Hypocotyl length of the lh mutant was neither affected by temperature regime nor light quality, while negative DIF reduced stem length with 15–20% compared to positive DIF due to a delayed internode elongation. The general response pattern in both genotypes was not affected by an additional reduction in DLI of 50%. In conclusion, the strongest effect of DIF was found under a LRFR which is the opposite of findings in earlier studies with day extentions with different light qualities. In general, HRFR reduced stem elongation of cucumber more than negative DIF. The results indicate a crosstalk between light phytochrome responses and thermoperidism.  相似文献   

12.
Chickpea is sensitive to chilling stress, especially at its reproductive stage and experiences abortion of flowers and poor pod set at temperatures below 10 °C. The metabolic controls governing chilling-sensitivity in chickpea, particularly involving proline are not known. Hence, in the present study we explored the role of proline in this regard. A set of chickpea plants (cv. GPF2) growing under warm conditions of the glass house (temperature – 28/14 °C as average maximum and minimum till early flowering stage) was exposed to low temperature conditions of the field (8.3–9.6/2.8–5.3 °C; average maximum and minimum temperature, respectively) during the onset of reproductive phase while another set of plants continued to grow under warm conditions. In case of chilling-stressed plants, one set of the plants was treated with 10 μM proline while the other set not treated with proline served as control under low temperature conditions. In untreated chilling-stressed plants, the endogenous proline increased to 230 μmol g−1 dry weight (DW) on 4th day of stress and decreased thereafter to reach 28 μmol on 7th day. In plants treated with 10 μM proline, its endogenous content reached 310 μmol g−1 DW on 4th day and stayed significantly higher than untreated chilling-stressed plants. The proline-treated plants showed significant improvement in retention of flowers and pods leading to better seed yield compared to the untreated ones. The proline-applied plants also had greater pollen viability, pollen germination, pollen tube growth and ovule viability. The stress injury measured as oxidative stress, electrolyte leakage, loss of chlorophyll and decrease in leaf water content was mitigated significantly in proline-treated plants. Additionally, proline application increased the level of sucrose and trehalose (cryoprotectants) in chilling-stressed plants. The studies revealed that proline application was significantly effective in reducing the impact of chilling injury on reproductive growth in chickpea.  相似文献   

13.
Changes in endogenous abscisic acid and soluble sugars levels during dormancy-release of lily bulbs of Lilium rubellum were investigated. Shoot emergence and flowering of the bulbs stored for 14 weeks at 4 °C occurred more synchronously, and the time span from first to last flower in the plants was shorter than those of bulbs stored for 10 weeks at 4 °C. Longer duration of bulb storage showed accelerating effects of increasing leaf number and stem length but negatively affected flower size. Flower number per plant was not much influenced by bulb storage duration. Concentration of endogenous abscisic acid (ABA) level in the bulbs during bulb storage decreased as storage duration increased, and it remained at a constant level after being stored for 10 weeks. This result suggests that the decrease in the endogenous ABA level during bulb storage is correlated with dormancy-release. Concentrations of soluble sugars also changed during bulb cold storage. Sucrose concentration increased as the chilling term increased to 10 weeks but decreased afterward. Glucose and fructose increased from the beginning of chilling to the end of a 14-week cold storage.  相似文献   

14.
In order to increase the fruit weight of a shriveled-seed cultivar, trees of ‘Yu Her Pau’ litchi (Litchi chinensis Sonn.) growing in Taiwan were sprayed with Gibberellic acid (GA3) (ProGibb®, 20% of GA3) at 5 and 10 mg/l 14 days after full bloom (AFB) over 2 years. Both concentrations of GA3 significantly increased fruit longitudinal and transversal diameter, and fruit, aril and pericarp weight (40–41 and 37–38 mm, and 27.3–28.4, 21.7–22.7 and 5.0–5.3 g, respectively) compared with control (35–36 and 33–34 mm, and 22.3–22.4, 17.8–17.9 and 3.9–4.0 g), but had no significant effects on seed weight, percentage of aril weight of total fruit weight or total soluble solids (0.5–0.7 g, 78.9–80.3% and 18.1–19.0 °Brix, respectively). Fruit characteristics within the two concentrations of GA3 showed no significant difference. The results indicated that sprays of GA3 should be evaluated in ‘Yu Her Pau’ commercial orchards, and in other elite cultivars.  相似文献   

15.
The flowering responses of Brunonia australis (blue pincushion) and Calandrinia sp. to vernalization, photoperiod, temperature and plant age were investigated to provide a foundation for manipulating flowering in these potential potted plants. Plants were vernalized at 4.8 °C for 0, 3 or 6 weeks at the plant age of 1–4 or 8–14 leaves. Following vernalization, plants were grown at 25/10 or 35/20 °C (day/night) under short days (11 h, ambient daylight averaged 380 ± 44 μmol m−2 s−1) or long days (16 h) provided by an additional 5 h night break (21:00–2:00 h at <4.5 μmol m−2 s−1 from incandescent lamps), for 85 days. This is the first work to investigate flowering of these ornamental species. Both species showed enhanced flowering following vernalization and a quantitative requirement for long days. The reduction of the time until the first visible inflorescence (Brunonia) or flower (Calandrinia) buds by 8–13 days was affected by vernalization for 3 or 6 weeks, respectively. Long days were effective for reducing the time to first visible floral bud and increasing the number of inflorescence or flowers per plant for both species. For Brunonia, LDs replaced vernalization when applied to plants with 1–4 leaves. Raising temperature from 25/10 to 35/20 °C increased the number of flowers per plant of Calandrinia by 2–2.5-fold for plants with 1–4 or 8–14 leaves respectively.  相似文献   

16.
Environmental control of the annual growth cycle of ‘Glen Ample’ raspberry has been studied in order to facilitate crop manipulation for out-of-season production. Plants propagated from root buds were raised in long days (LD) at 21 °C and then exposed to different temperature and daylength conditions at varying ages. Shoot growth was monitored by weekly measurements and floral initiation by regular sampling and examination of axillary bud #5. Under natural summer daylight conditions at 60°N shoot growth was nearly doubled at 21 °C compared with 15 °C, while at 9 °C one half of the plants ceased growing and formed flower buds at midsummer. Developing shoots have a juvenile phase and could not be induced to flower before the 15-leaf stage. No significant reduction in induction requirements was found in larger plants. Plants exposed to natural light conditions from 10th August, had an immediate growth suppression at 9 and 12 °C with complete cessation after 4 weeks (by September 7). This coincided with the first appearance of floral primordia. At 15 °C both growth cessation and floral initiation occurred 2 weeks later (by September 21), while at 18 °C continuous growth with no floral initiation was maintained until early November when the photoperiod had fallen below 9 h. The critical photoperiod for growth cessation and floral initiation at 15 °C was 15 h. Plants exposed to 10-h photoperiods at 9 °C for 2–4 weeks had a transient growth suppression followed by resumed growth under subsequent high temperature and LD conditions, while exposure for 5 or 6 weeks resulted in complete growth cessation and dormancy induction. The critical induction period for floral initiation was 3 weeks although no transitional changes were visible in the bud before week 4. When exposed to inductive conditions for marginal periods of 3 or 4 weeks, an increasing proportion of the plants (20% and 67%, respectively), behaved as primocane flowering cultivars with recurrent growth and terminal flowering. It is concluded that growth cessation and floral initiation in raspberry are jointly controlled by low temperature and short day conditions and coincide in time as parallel outputs from the same internal induction mechanism.  相似文献   

17.
The effects of mean daily temperature (MDT) and mean photosynthetic daily light integral (MDLI) on flowering during the finish stage of two petunia (Petunia × hybrida) cultivars were quantified. Petunia ‘Easy Wave Coral Reef’ and ‘Wave Purple’ were grown in glass-glazed greenhouses at 14–23 °C or 14–26 °C and under 4–19 mol m−2 d−1 with a 16-h photoperiod. The flower developmental rate was predicted using a model that included a linear MDT function with a base temperature multiplied by an exponential MDLI saturation function. The flower developmental rate increased and time to flower decreased as MDT increased within the temperature range studied. For example, under a MDLI of 12 mol m−2 d−1, as MDT increased from 14 to 23 °C, time to flower of ‘Easy Wave Coral Reef’ and ‘Wave Purple’ decreased from 51 to 22 d and 62 to 30 d, respectively. Flower developmental rate increased as MDLI increased until saturation at 14.1–14.4 mol m−2 d−1. Nonlinear models were generated for effects of MDT and MDLI on flower bud number and plant height at flowering. The number of flower buds at flowering increased as MDT decreased and MDLI increased. For example, at an MDT of 14 °C with 18 mol m−2 d−1, plants had 2.5–2.9 times more flower buds than those grown at 23 °C and 4 mol m−2 d−1. Models were validated with an independent data set, and the predicted time to flower, flower bud number, and plant height were within ±7 d, ±20 flowers, and ±4 cm, respectively, for 96–100%, 62–87%, and 93–100% of the observations, respectively. The models could be used during greenhouse crop production to improve scheduling and predict plant quality of these petunia cultivars.  相似文献   

18.
Changes in membrane lipid composition are important in the acclimation of plants. The influence of four day/night growing temperature combinations (18/12, 25/12, 25/22, and 30/22 °C) on membrane lipids of ‘Earliglow’ and ‘Kent’ strawberry (Fragaria × ananassa Duch.) were studied. The monogalactosyl diglyceride (MGDG) and digalactosyl diglyceride (DGDG) were the major galactolipids in the strawberry leaves. ‘Earliglow’ contained a higher amount of galactolipids in the leaves than ‘Kent’. The major phospholipids in the strawberry leaves, roots, and fruit were phosphatidylcholine (PC), phosphatidylinositol (PI), phosphatidylglycerol (PG), and phosphatidylethanolamine (PE). PC and PE were the two predominant phospholipids in the strawberry. The leaves and fruit of ‘Earliglow’ contained higher amounts of phospholipids compared to those of ‘Kent’, whereas ‘Kent’ strawberry roots had higher phospholipids. Palmitic (C16:0), stearic (C18:0), oleic (C18:1), linoleic (C18:2), and α-linolenic (C18:3) acids were major fatty acids in galacto- and phospholipids of the ‘Earliglow’ and ‘Kent’ strawberry. PC is very rich in linolenic acid in leaves compared to the fruit and root tissues. PC had the highest ratio of unsaturated to saturated fatty acids among all phospholipids. There was a significant increase in the content of galactolipids (MGDG, DGDG) and phospholipids (PC, PI, PG and PE) and unsaturation of their fatty acids in the cool day/night growth temperature. Increasing day/night growth temperatures decreased MGDG/DGDG ratios. The shifts in saturation and composition of fatty acids observed with strawberry may be an adaptation response of plants to the temperature changes.  相似文献   

19.
The influence of seed maturity, seed storage and germination pre-treatments on seed germination of cleome (Cleome gynandra L.) were investigated. Seed maturation studies showed that capsules harvested at 18 days after anthesis possessed the highest dry weight with 19.2% moisture and 1% germination. Development of fresh-ungerminated seed was observed with increasing maturity of fruit, suggesting that cleome exhibited forms of seed dormancy. Storing mature seed at 15 °C and at room temperature for 5 months showed that seed dormancy was broken after 3 months under both storage regimes. When mature seeds were subjected to different treatments including various levels of GA3, KNO3, leaching, pre-chilling, soaking and pre-heating at different temperatures, it was found that pre-heating at 40 °C for period of 1–5 days was the most effective method in breaking dormancy in cleome.  相似文献   

20.
Fruit development was investigated in the field in over-winter off-season (bloomed in late November) and on-season (bloomed in mid April) longans (Dimocarpus longan Lour. cv. Chuliang) in 2004–2005 and 2007–2008 crops, and in potted trees grown in phytotrons set at cold (15/10 °C, day/night, simulating winter) or warm temperatures (28/23 °C, day/night) in 2008. Development of fruit in both on-season and off-season longans could be divided into two stages based on the pattern of fresh weight increase. Stage I was characterized by the slow fruit growth, and Stage II by rapid fruit growth with aril expansion. Off-season longan had a longer period of fruit development than on-season longan, chiefly due to a longer Stage I. The development of off-season fruit, especially in Stage I, was exposed to low and abruptly fluctuating temperatures. In contrast, the temperatures during on-season fruit growth were warmer and less fluctuating. Off-season fruit were smaller with a significantly higher fruit drop. Intensive fruit drop did not occur during cold period until temperature had risen. Fruit cracking in off-season longan was severe (27.6%) in 2004–2005 with a dry and cold winter, but negligible in 2007–2008 with a wet and cold winter. In phytotron experiment, trees exposed to the cold temperature regime during early fruit development produced significantly smaller fruit compared to those exposed to the warm temperature regime (6.2 g vs 7.3 g), while there was no significant difference in fruit drop rate and cracking incidence. The results suggested temperatures lower than 15 °C were stressful for the growth of young fruit and reduced the growth potential and thus fruit size. Severe fruit drop in over-winter off-season longan might be associated with stressful cold plus abrupt temperature fluctuations, while severe fruit cracking in over-winter off-season longan might be related to cold and dry weather in the winter.  相似文献   

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