Temperature effects on flower formation in saffron (Crocus sativus L.)

The temperature conditions for shoot growth and flower formation were characterised for saffron (Crocus sativus L.). Leaf withering occurred during late winter or spring depending on location, and coincided with a rise in temperature. No growth was detectable in the buds during the first 30 days after leaf withering, neither in underground corms nor in lifted corms incubated in the laboratory under controlled conditions. Flower initiation occurred during the first growth stages of the buds. The optimal temperature for flower formation was in the range from 23 to 27 °C, 23 °C temperature being marginally better. To ensure the formation of a maximum number of flowers, the incubation at these temperatures should exceed 50 days, although incubation longer than 150 days resulted in flower abortion. Flower emergence required the transfer of the corms from the conditions of flower formation to a markedly lower temperature (17 °C). Incubation of the corms after lifting at a higher temperature (30 °C), reduced flower initiation and caused the abortion of some of the initiated flowers. No flowers formed in corms incubated at 9 °C. A variable proportion (20–100%) of the corms forced directly at 17 °C without a previous incubation at 23–27 °C formed a single flower. The wide differences in the timing of the phenological stages in different locations we found in this study seemed related to the ambient temperature. Leaf withering was followed shortly by flower initiation, which occurred during late spring or early summer as the rising temperature reached 20 °C. A long hot summer delayed flower emergence which occurred in late autumn as the temperature fell to the range of 15–17 °C.     

Temperature effects on corm dormancy and growth of Zephyra elegans D.Don

Experiments were performed with the Chilean geophyte Zephyra elegans, a potential cut flower, to evaluate the effect of corm weight and storage temperature on corm dormancy, and to determine the effect of day and night growing temperatures on its growth and flowering. Z. elegans has a deciduous and synanthous growth habit and the corm is replaced annually. Dormant corms were stored at different constant temperatures or temperature combinations from 20 to 40 °C. Corms released from their dormancy were grown at 15/10, 20/15, or 25/20 °C day/night temperatures. Corms of various weights were planted at the same date after being stored dry at 25 °C for 22 weeks. They all emerged 19–38 days after planting, showing that dormancy release was not affected by corm weight. A 20-week corm storage treatment at a constant 25 °C resulted in the most rapid corm sprouting. Sprouting percentage was reduced at higher or lower storage temperatures. Temperature also affected plant growth. When plants were grown at 15/10 or 20/15 °C they emerged and flowered more rapidly than when they were grown at 25/20 °C. The latter growing temperature also resulted in poor flower quality.     

Day and night temperatures,daily light integral,and CO2 enrichment affect growth and flower development of Campanula carpatica ‘Blue Clips’

Campanula carpatica Jacq. ‘Blue Clips’ plants were grown in a greenhouse under nine combinations of day and night temperatures created by moving plants every 12 h among three day/night temperatures (15, 20, and 25°C). At each temperature, there were three daily light integrals (DLI; 4.2, 10.8, and 15.8 mol m⁻² per day, averaged over the experimental period) created with varying supplemental light, and ambient (≈400 μmol mol⁻¹) and enriched (≈600 μmol mol⁻¹) CO₂ concentrations. Time to flower was closely related to average daily temperature (ADT), and was not significantly affected by the day or night temperatures delivered to achieve a specific ADT. Time to flower was not largely affected by DLI or CO₂ enrichment. As plant ADT increased between 15 and 25°C, flower diameter decreased about 1 mm per degree and was not related to the difference between day and night temperatures (DIF). Flower diameter was smallest and least sensitive to changes in temperature at lower DLI and at ambient CO₂ levels. There were 10 less flower buds and 0.3 g less dry mass per plant at first flower for every 1° increase in plant ADT at high and medium DLIs. Flower bud number and dry mass were relatively low and less sensitive to changes in ADT at low DLI, and increased slightly with CO₂ enrichment at medium and high but not at low DLI. Plant height was not related to ADT, but increased linearly as DIF increased from −6 to 12°C at all DLIs, but the response was stronger under low DLI than high and medium DLIs. Flower bud number and dry mass were correlated closely with the ratio of DLI to daily thermal time (base temperature of 0°C). Flower bud number and dry mass were highest when C. carpatica plants were grown at 15°C with a DLI of 10–15 mol m⁻² per day.     

Effects of pre-blossom temperatures on flower development and fruit set in apricot

The influence of pre-blossom temperatures on flower development and fruit set is ascertained in apricot (Prunus armeniaca L.), a species without previous records on the effect of pre-blossom temperature on fruit set, but that is particularly prone to erratic fruit set. A polyethylene cage was used during pre-blossom development of flower buds to increase maximum temperatures by 6–7 °C and mean temperatures by 3 °C in orchard conditions. This increase in temperature accelerated flower bud development, caused a hastening in flowering time and following hand-pollination, reduced fruit set. At anthesis, flowers that had developed in warmer conditions weighed less and showed less development of the pistil than control flowers. Pistil growth of flowers under warm conditions did not differ from that of the control flowers when both the populations were compared on a real time scale in spite of the fact that warmed buds were at an advanced external phenological stage. Thus, hastening of external floral development by warm pre-blossom temperatures was not accompanied by advance in pistil development. This lack of synchrony resulted in premature flowering of flowers with underdeveloped pistils that had a reduced capability to set fruit. The results are discussed in terms of flower quality and its implications in fruit set and subsequent crop load.     

Flowering of Primula malacoides in response to photoperiod and temperature

Primula malacoides Franch. ‘Prima Lilac’ was grown at 16 or 20 °C in combination with short days (SD, 8 h) or long days (LD, 16 h). In addition to uninterrupted growing conditions, plants within each temperature were moved at weekly intervals to the other photoperiod and left until termination. Temperature, but not photoperiod, significantly affected the rate of development from start of treatments (51 days from seeding) to 2 mm visible flower bud (VB). At 16 °C, VB averaged 30 days and at 20 °C, 48 days. Time to flower (first horizontal petals) at 16 °C increased from 56 to 64 days as SD increased from 1 week to continuous conditions while LD decreased time to flower from 64 to 56 days. Time to flower at 20 °C varied from 73 to 87 days with additional SD exposure resulting in slower and LD in faster flowering. These observations of the flowering response in ‘Prima’ are contrary to the photoperiodic classification of P. malacoides as a SD plant.     

The temperature and photoperiod regulation of flowering and runnering in the strawberries,Fragaria chiloensis,F. virginiana,and F. x ananassa

The temperature and photoperiod interactions of a number of elite genotypes of Fragaria virginiana, F. x ananassa, and F. chiloensis were studied in a series of growth chamber experiments. Several parameters were evaluated including: (1) the critical day-length (CDL) for flowering of short day (SD) genotypes under 8, 9, 10, and 11 h days at 18 °C, (2) the floral and runnering response of single and multiple cropping genotypes under 8 and 16 h days at 18 °C, and (3) the effect of temperature on flower bud formation in day-neutral (DN) genotypes held at 18, 22, 26, and 30 °C under 12 h day-lengths. The same number of flowers were initiated under 15 and 30 day induction periods, regardless of photoperiod. Frederick 9, LH 50-4 and RH 30 (F. virginiana), ‘Aromas’ and ‘Tribute’ (F. x ananassa) and CFRA 0368 of F. chiloensis flowered under both long days (LDs) and SDs; while Eagle-14 (F. virginiana), ‘Fort Laramie’ and ‘Quinalt’ (F. x ananassa) flowered only under long days. While those genotypes that flowered under both LD and SD can be considered day-neutral, they varied in the degree of floral response to the two photoperiods. CFRA 0368 and Frederick 9 produced the same number of flowers under both LDs and SDs, while ‘Aromas’ and ‘Tribute’ had more flowers under LDs and RH 30 had more under SDs. Of the DN genotypes, LH 50-4 and RH 30 were the only ones that produced runners under SDs. Flowering in ‘Fort Laramie’ was least affected of any genotype by high temperature, although its dry weight was negatively impacted. Based on these data, several genotypes show promise as breeding parents: CFRA 0368 and Frederick 9 to equalize flower production under LD and SD conditions, LH 50-4 and RH 30 to produce more freely runnering DNs, and ‘Fort Laramie’ for floral heat tolerance.     

The impact of photoperiod and irradiance on flowering of several herbaceous ornamentals

Forty-one herbaceous species were grown under short-days (8 h photoperiod, ambient irradiance averaged 12–13.2 and 6.4–8.3 mol m⁻² day⁻¹ for Experiments I and II, respectively) with or without supplemental high-pressure sodium lighting (+50, 100, or 150 μmol m⁻² s⁻¹); or under long-days delivered using natural day lengths and irradiance with night interruption lighting (2200–0200 h at 2 μmol m⁻² s⁻¹ from incandescent lamps) or under ambient daylight plus supplemental irradiance during the day and as a day extension to 18 h (0800–0200 h) with supplemental high pressure sodium lighting (+50, 100, or 150 μmol m⁻² s⁻¹) to identify the impact of photoperiod and irradiance on flowering of each species. Days to first open flower, leaf number below first flower, and mean dry weight gain per day (MDWG) were measured when the first flower opened. Twenty-seven species were photoperiodic with examples of five photoperiodic response groups represented: obligate short-day (2), facultative short-day (5), obligate long-day (16), facultative long-day (4); 13 were day neutral (no photoperiod response in flowering). One species, Salvia sclarea L., did not flower. A facultative irradiance response was observed with 10 species; 28 species were irradiance indifferent; 2 had delayed flowering as irradiance increased. Photoperiod affected MDWG of 30 species. Increasing irradiance affected MDWG with 14 species. Photoperiod interacted with irradiance to affect MDWG of 11 species. Cobaea scandens had the greatest MDWG (0.40 g day⁻¹) while Amaranthus hybridus had the least MDWG (0.01 g day⁻¹) across photoperiod and irradiance levels.     

Combining ability among male sterile two-type and restorer lines of Zinnia elegans and implications for the breeding of this ornamental species

Nineteen parental lines including five male sterile A-lines (AH002A, AH003A, AH209A, S5001A, J16A) and fourteen restorers (A1-GH, A3, S5, J6, J7N, J7J, J8, J9, J10, J11, J12, J13, J14, J17) were crossed using the North Carolina II statistical method. Studies of combining ability and heritability were conducted on selected parents along with their seventy F₁ hybrids for main ornamental traits. Plant height, crown size and length of node had obvious additive genetic effects, high (>0.50) broad sense heritability and high narrow sense heritability (length of node was medium). Pedicel length showed approximately equivalent maternal and paternal additive genetic effects, high broad sense heritability and medium (0.30–0.50) narrow sense heritability. Number of whorls of ray florets across capitulum and number of branches were able to take advantage of heterosis. The relationship between general combining ability and specific combining ability in Zinnia elegans depended on materials and traits. Male sterile two-type line was pivotal in the hybridization breeding of Z. elegans. S5001A, AH002A and A1-GH, A3, J14 which performed high negative GCA effects in PH, PL, LN and type I in PH, PL, NW, LN were ideal female and male parents of potted flowering plants; AH209A, J16A and S5, J10, J17 which displayed positive GCA effects and almost type I in PH, PL, LN were ideal female and male parents of cut flowers, respectively. For potted flowering plants, AH002A × J17, AH209A × A1-GH and S5001A × J6 with high negative SCA effects in PH, PL and LN were the most promising combinations, AH002A × S5, AH003A × A3 and J16A × J6 were the subprime combinations; for cut flowers, AH209A × S5, AH209A × J17 and J16A × J17 with high positive SCA effects in PH, PL and LN were the primary combinations, AH209A × J9 and S5001A × J10 were the secondary combinations.     

Production of high quality Ardisia plants by stem tip cuttings

To produce commercially acceptable Ardisia plants, stem tip cuttings from mature plants were rooted and forced in greenhouses. Ten centimeter long cuttings were either treated with 200 ppm 1-naphthalene acetic acid (NAA) for 2 h, 2000 ppm indole-3-yl-butyric acid (IBA) for 10 s, or 0.5 and 1.0% IBA powder prior to sticking them in the rooting medium. Rooting percentage at 45 days exceeded 76% with 2000 ppm IBA treatment which was a significant increase over non-treated control. Rooted cuttings developed into three types of plants: those forming only vegetative shoots without flowers, those forming reproductive shoots with flowers, and those forming both vegetative and reproductive shoots. The ideal plant produced only vegetative shoots when rooted cuttings were transplanted into pots. About 50% rooted cuttings were forced to finish, producing 31 or 40% of high quality plants when rooted cuttings with vegetative shoots were grown in a greenhouse (GH) at temperatures higher than 21/19 °C (day/night) in 1995 or 21/18 °C GH in 1997, respectively. This method shortened the total production time to less than 2 years as compared to 4 years when starting from seeds.     

Influence of temperature and bark injuries on the development of Phytophthora cactorum and P. Citrophthora on peach trees

The effect of temperature and bark injuries on the occurrence of crown rot of peach trees caused by P. cactorum and P. citrophthora were examined in field and laboratory. Lesions developed at 35 °C (the complete range of temperatures tested) but maximum development occurred at 20–25 °C. Greatest growth of these fungi on cornmeal agar (CMA) also occurred between 15 and 30 °C. Both pathogens could infect injured trees up to 20 days after wounding, but could not infect uninjured plants or plants wounded 40 and 30 days before inoculation, respectively. This study showed that temperature is a critical factor for the development of Phytophthora crown rot of peach trees. In addition, crown rot developed from recent wounds inoculated with agar plugs of Phytophthora.     

Freezing temperature treatment induces bud dormancy in ‘Granny Smith’ apple shoots

One-year-old, ‘Granny Smith’ apple (Malus × domestica Borkh.) shoots were selected randomly from commercial orchards in 1999 and 2003, cold stored at temperatures between 1 and 13 °C for varied periods, following a 12/12 h freezing temperature pre-treatment of −1/13 °C (supposedly non-chilling temperatures) for 1 or 2 weeks. The rate of budburst, determined after forcing at 25 °C, was used to follow the progression of bud dormancy. The freezing pre-treatment clearly enhanced (deepened) bud dormancy in all experiments. Clearly definable influences due to the presence of leaves during the pre-treatment were not observed on shoots cold stored at chilling temperatures. Trees were defoliated before leaf drop in late summer/autumn under field conditions by hand (2001) and using a spray containing 3% urea and 1.8% zinc sulphate in 2003. In 2001 the first two hand defoliation dates significantly enhanced dormancy, while in 2003 chemical defoliation had no effect. These data indicate that the leaves are not clearly involved in the perception of factors that are responsible for dormancy induction. As with dormancy release it is possible that the perception of induction factors, i.e. low temperatures, and as shown in these data, freezing temperatures, occurs within the buds themselves.     

GA4+7 plus benzyladenine reduce foliar chlorosis of Lilium longiflorum

The effectiveness of two commercial formulations of gibberellin (GA) and benzyladenine (BA) for reducing foliar chlorosis on Easter lily (Lilium longiflorum Thunb.) was compared. On a per liter basis, plants were sprayed with 0, 100, 200, or 400 mg (BA equivalent) of Accel (GA₄₊₇:BA of 1:10) or Promalin (GA₄₊₇:BA of 1:1) when the crop leaf area index (LAI)=3. One group of plants was sprayed with 100 mg of Accel or Promalin (BA equivalent) per liter twice: once at LAI=3 and again 3 weeks later. Plants were harvested when the largest flower bud on each plant measured 13 cm in length, stored for 0 or 3 weeks at 2.5°C in the dark, and then moved into a post-harvest evaluation room at 21°C, where foliar chlorosis was monitored for 3 weeks. Senescence of some lower leaves on plants in every treatment was evident at harvest, and incidence of senescence increased during the 21 days of post-harvest evaluation. Cold storage increased the number of leaves senescing during the subsequent evaluation period. Application of Promalin or Accel significantly reduced leaf senescence compared to that of untreated plants. At harvest, 21% of the leaves on untreated plants were senescent, while plants treated with Promalin or Accel averaged 3 or 9% senescent leaves, respectively. Following 7 days of post-harvest evaluation, Promalin was more effective in preventing chlorosis than Accel at the 400 mg l⁻¹ (BA equivalent) level. Following 14 or 21 days of post-harvest evaluation, Promalin was more effective than Accel for the 100 mg l⁻¹ 2× and 400 mg l⁻¹ (BA equivalent) treatments.Plants in all Promalin and Accel treatments were taller than untreated plants 1 week after sprays were applied. At harvest, plants sprayed with Promalin were between 6 and 14 cm taller than untreated plants, but those treated with Accel were the same height as untreated plants.Neither Promalin nor Accel influenced the occurrence of malformed or aborted flowers in this study. However, cold storage significantly increased the number of plants with aborted buds and malformed flowers. Unstored plants averaged 0.16 aborted buds and 0.02 malformed flowers each, while those stored 3 weeks averaged 0.51 aborted buds and 0.18 malformed flowers each.     

Environmental factors affecting flowering of rice flower (Ozothamnus diosmifolius,Vent.)

Rice flower (Ozothamnus diosmifolius, Vent.), native to east Australia, is a spring flowering perennial shrub. It is a new cut flower plant, recently introduced into cultivation in Australia and in Israel. Its response to environmental conditions, which affect growth and flowering, are not yet known. The purpose of the present study was to evaluate the effects of growth temperature, photoperiod and total solar energy on flowering. Experiments were conducted with plants of the cv. Cook’s Snow White. Plants were grown in three cycles under controlled conditions in the phytotron, at four day/night temperature regimes: 17/9, 20/12, 23/15 and 26/18°C. Two photoperiods — short day (SD) of 10 h natural day light and long day (LD) of 10 h natural light plus 10 h incandescent light — were employed. High temperatures enhanced vegetative growth but blocked flowering under both LD and SD. Under medium–moderate temperatures plants were absolute LD plants and did not flower under SD conditions. Under lower temperatures plants flowered under both LD and SD, but SD delayed flowering. High total solar radiation under LD did not affect flowering time but greatly promoted the number of flowering stems.     

Interaction of temperature and vegetative flush maturity influences shoot structure and development of lychee (Litchi chinensis Sonn.)

Potted lychee trees (cv. Tai so) of varying vegetative flush maturity were grown under a range of temperature regimes and monitored for subsequent shoot structure and development. A combination of low temperature (15/17 or 18/13 °C day/night) and high vegetative flush maturity was necessary for floral initiation to occur. Exposure to high temperatures (28/23 °C) invariably resulted in the production of vegetative shoots, irrespective of flush maturity. Strong floral initiation was marked by the emergence of terminal panicles and accompanying axillary panicles. A decrease in vegetative flush maturity or increase in temperature (e.g. 23/18 °C) resulted in a decrease in axillary shoot formation and the production of several intermediate shoot structures. These included leafy panicles, stunted panicles, partially emerged buds and non-emergent swollen buds, often produced on the same tree. At 23/18 °C, closer synchronisation of initial flush maturity was required for the production of a consistent shoot-type. Trees with synchronised mature flushes (I-2) at 23/18 °C resulted in the production of swollen terminal buds. Healthy trees were maintained in this state for at least 11 months. These results indicate that both temperature and flush maturity can influence subsequent shoot structure of lychee. In the absence of either a strong floral temperature (18/13 °C) or strong vegetative temperature (28/23 °C), slight differences in initial flush maturity have greater impact on the type of emerging shoot formed.     

Bruising injury of persimmon (Diospyros kaki cv. Fuyu) fruits

This study was performed to monitor the deterioration of bruised persimmon (Diospyros kaki cv. Fuyu) fruits. Freshly harvested fruits were bruised by dropping them from a height of 50 cm onto a steel board and then stored at 0 or 20 °C in temperature controlled chambers for up to 4 weeks. Immediately after the bruising, no visible injury on the fruits was evident, but the fruits deteriorated rapidly during storage. The skin tissues of the fruits stored at 20 °C became more reddish with the duration of the storage, but no such changes were found with the fruits stored at 0 °C. The increase in redness of the skin tissues appeared to be associated with storage temperature, but not with the bruising. The skin tissues also became darker when stored at 20 °C than at 0 °C and this tendency was more obvious with the bruised fruits. Flesh firmness decreased rapidly during storage except for the non-bruised fruits stored at 0 °C. Even the non-bruised fruits rapidly lost their flesh firmness at 20 °C. No significant changes in lipid peroxidation, as expressed by malondialdehyde production, were found between the bruised and the non-bruised fruits during the storage either at 0 °C or at 20 °C. This implies that the fruit deterioration caused by bruising is not due to the consequences of lipid peroxidation. Polyphenol oxidase activity increased more rapidly in the bruised fruits than in the non-bruised fruits during storage. The bruising had more effect on increasing polyphenol oxidase activity than did the storage temperature. Although the increase in polyphenol oxidase activity appeared to be associated with the visual deterioration of the bruised fruits, it did not exactly correspond to the physical deterioration. These results indicate that polyphenol oxidase is not the only factor influencing the deterioration associated with bruising. Cell wall hydrolases are currently being assayed to determine if they also contribute the deterioration following bruising.     

Cultivation of cut flower and bulb species with saline water

The long-term effect of saline water irrigation on flower yield and quality was investigated in three herbaceous cut flower crops of commercial importance, the Emily cultivars of Japanese limonium, Trachelium caeruleum and Eustoma grandiflorum (lisianthus), and in two bulb species, Hippeastrum hybridum and Ornithogalum arabicum. Among the tested crops, limonium showed the highest resistance to salinity. Irrigation water with an electrical conductivity of up to 11.5 dS m⁻¹ had little or no effect on stem yield and length of limonium flowering stems. In Trachelium, salinity had no effect on the yield of flowering stems or the size of the inflorescence, but it markedly reduced stem weight and length. The concomitant reduction in the number of nodes to flowering was reflected in earlier flower initiation. Since delayed flower differentiation and over-elongation of Trachelium stems is a serious problem during the winter months, application of mildly saline irrigation for winter production could be used to induce earlier flower initiation and to control stem height. In lisianthus subjected to salinity from bud appearance onwards, a salinity level of 6.0 dS m⁻¹ increased stem weight and the number of flowers per stem without affecting other quality parameters. The work carried out with Trachelium and lisianthus, although limited, indicates that salinity may be used for improving the quality of some cut flowers. In contrast to its beneficial effect on the herbaceous species, salinity led to a significant reduction of bulb, leaf, and root weight of the two bulbous species, H. hybridum and O. arabicum.     

The association between low temperatures and anatomical changes in preanthetic ovules of Musa (Musaceae)

Bananas growing in subtropical environments suffer tissue malformation in fruit structures that is associated with mean daily temperatures of about 14 °C during differentiation of the fruit tissues. Low temperatures may also affect the pre-anthetic ovules and contribute to loss of functionality in reproductive structures. Ovules of Musa acuminata Colla ssp. that experienced a range, 3–18 °C, of minimum temperatures in the field, were examined for anatomical changes. We assumed that low temperatures caused the changes by association with the gross abnormalities of flower structure described in the literature. The first sign of anatomical changes in ovules associated with low temperature was the protrusion of the nucellus and nucellar cap through the micropyle forming a tongue, which often contained the embryo sac. Malformed ovules were found next to normal ones, especially in ovaries that displayed no outward signs of malformation associated with low temperatures.The ovules affected by low temperature were smaller, grew less between developmental stages and remained more round towards anthesis than those that were unaffected. Affected ovules had smaller female gameotphytes that occupied a reduced proportion of the nucellus. In addition, the distance between the embryo sac and the nucellar cap increased, however the number of intervening cells did not. The nucellar cells in the tongue were squashed longitudinally. Malformations of ovules were observed in bunches emerging in the autumn and winter as well as spring, associated with low temperatures at a critical period in the few weeks before anthesis when the archesporia and megaspore were formed.     

Embryo induction via anther culture in papaya and sex analysis of the derived plantlets

We investigated the embryo induction of papaya by anther culture, and identified the sex of plantlets derived from embryos using a sex-diagnostic PCR. Anthers, containing approximately 80% uninucleate pollen, were collected from 10 to 14 mm long male flower buds. They were pre-treated on agar (0.8%) or in liquid medium for 1–5 days at 25 or 35 °C, then transferred to agar medium with 0.1 mg l⁻¹ BA and 0.1 mg l⁻¹ NAA. Agar and liquid media used for the pre-treatment contained water only or MS nutrients with or without sucrose (2.0%). On the agar medium, no embryos were induced at any pre-treatment temperature. In the liquid medium at 25 °C, embryos were induced at about 1.0% (rate of anthers forming embryos) in MS medium with sucrose for 3 or 5 days. At 35 °C, embryo induction rate tended to increase up to about 4.0% when anthers were treated in water for 1 day or MS medium with sucrose for 3 or 5 days. The sex of plantlets established through anther culture was analyzed using a sex-diagnostic PCR. All plantlets were determined as female. From these results, we suggest that all plantlets established through anther culture were of microspore origin, and that the anther culture technique is useful for the breeding of female papaya.     

The influence of increasing tree cover on mean radiant temperature across a mixed development suburb in Adelaide,Australia

The implementation of trees in urban environments can mitigate outdoor thermal stress. Growing global urban population and the risk of heatwaves, compounded by development driven urban warmth (the urban heat island), means more people are at risk of heat stress in our cities. Effective planning of urban environments must minimise heat-health risks through a variety of active and passive design measures at an affordable cost. Using the Solar and Longwave Environmental Irradiance Geometry (SOLWEIG) model and working within the bounds of current urban design, this study aimed to quantify changes in mean radiant temperature (T_mrt) from increased tree cover at five different 200 × 200 m urban forms (including compact mid-rise development, residential and open grassy areas) within a suburb of Adelaide, Australia during summer. Following a successful validation of SOLWEIG, street trees were strategically distributed throughout each of the five urban forms and the model run over five warm sunny days (13–17 February 2011). Results showed spatially averaged daytime (7:30–20:00) T_mrt reduced by between 1.7 °C and 5.1 °C at each site, while under peak heating conditions (16 February, 14:00) T_mrt reduced by between 2.0 °C and 7.1 °C. The largest reduction in T_mrt under peak warming conditions was at the residential site, despite having the fewest number of trees added. Directly below clusters of trees, T_mrt could be reduced by between 14.1 °C and 18.7 °C. SOLWEIG also highlighted that more built-up sites showed higher T_mrt under peak warming conditions due to increased radiation loading from 3D urban surfaces, but over the course of the day, open sites were exposed to greater and more uniform T_mrt. This study clearly demonstrates the capacity of street trees to mitigate outdoor thermal stress and provides guidance for urban planners on strategic street tree implementation.     

Decreased anthocyanin biosynthesis in grape berries grown under elevated night temperature condition

In grape cultivation, high night temperature generally reduces anthocyanin accumulation in berry skin. To clarify the regulatory mechanism of anthocyanin biosynthesis under the conditions of high night temperatures, we examined flavonoid accumulation, the activities of related enzymes and gene expression in the anthocyanin biosynthetic pathway in grape berries grown under cool and warm night conditions. Anthocyanin accumulation in the skin of berries grown at high night temperatures (30 °C continuous) was reduced as compared to that of berries grown at low night temperatures (30 °C in daytime/15 °C in night time). On the other hand, flavonol levels in the skin of berries were not significantly different between low and high night temperature conditions. High night temperatures also inhibited the gene expression of chalcone synthase (CHS), flavanone 3-hydroxylase (F3H), dihydroflavonol 4-reductase (DFR), leucoanthocyanidin dioxygenase (LDOX) and UDP-glucose: flavonoid 3-O-glucosyltransferase (UFGT) at veraison and an increase in UFGT activity after veraison. These results suggest that the inhibition of anthocyanin biosynthesis in grape berries grown under high night temperature condition could be caused by lower expression levels of anthocyanin biosynthetic genes at an early stage of ripening and lower activities of anthocyanin biosynthetic enzymes, particularly UFGT.