Abstract
Plants of Hydrangea macrophylla Thunb. were grown in various environments to identify factors responsible for the appearance of malformed hydrangea leaves and to screen cultivars for tolerance to the foliar disorder. Ambient temperature, photosynthetic photon flux (PPF), and root system temperature were studied. Hydrangea leaf malformation is under thermal control and can be stimulated by ambient temperatures of 33/26C (light/dark), but these must be maintained to sustain the development of distorted foliage. Placement of plants with malformed leaves into a 26/22C (light/dark) environment resulted in subsequent development of typical leaves. A PPF of 506 μmol·s−1·m−2 resulted in a more rapid appearance of distorted leaves than a PPF of 224 μmol·s−1·m−2. Reducing the root system temperature below the ambient level of 32/28C to 20/18C (light/dark) reduced, but did not prevent, the development of malformed leaves. ‘Blau Donau’ and ‘Tricolor’ did not develop malformed foliage during 22 weeks of growth at 32/26C (light/dark). ‘Rose Supreme’, ‘Merritt's Supreme’, ‘Rosa Rita’, and ‘Dr. Bernard Steiniger’ had developed malformed leaves by week 8 of treatment. For ‘Rose Supreme’ and ‘Blau Donau’, leaves developing at the higher temperatures had shorter and narrower laminae, less fresh weight and surface area, and more dry weight per unit area than plants at the lower temperatures. Laminae developing at the higher temperatures were thicker due to an increase in adaxial palisade parenchyma tissue. Malformed ‘Rose Supreme’ leaves had fewer intercellular spaces than normal leaves and lacked an observable spongy parenchyma layer. However, laminae of ‘Blau Donau’ leaves developed a distinct, yet thinner, spongy parenchyma layer at the higher than at the lower temperatures; intercellular spaces were still prevalent in the spongy parenchyma layer at the higher temperatures.
The diffusion coefficient of CO2 in `Russet Burbank' potato (Solanum tuberosum L.) tubers was determined under steady-state conditions at 10 and 27C. The data showed that the skin is the main barrier to gas diffusion, with an average diffusion coefficient of 6.57 × 10-7 and 7.61 × 10-7 cm·s-1 at 10 and 27C, respectively. The flesh also presents an appreciable barrier to gas diffusion. The average diffusion coefficient of CO2 in the flesh was 2.00 × 10-4 and 2.24 × 10-4 cm·s-1 at 10 and 27C, respectively. Under regular storage conditions, the tuber is well aerated and the concentration of O2 at the center of the tuber is sufficient to maintain aerobic respiration.
Ilex crenata Thunb. `Rotundifolia' split-root plants were grown for 3 weeks with root zones at 30/30, 30/34, 30/38, 30/42, 34/34, 38/38, and 42/42C. The 38C root-zone treatment was the upper threshold for several growth and physiological characteristics. A portion of the root system grown at or near the optimum temperature could compensate, in terms of shoot growth, for part of the root system exposed to supraoptimal root-zone temperatures up to 38C. Higher root-zone temperatures did not affect short-term photosynthetic rates or root : shoot ratios, but altered photosynthate partitioning to various stem and root sinks. Although no differences were found for total 14C partitioned to the roots, partitioning of 14C into soluble and insoluble fractions and the magnitude of root respiration and exudation were influenced by treatment. Heating half of a root system at 38C increased the amount of 14C respired from the heated side and increased the total CO2respired from the nonheated (30C) half. Exposure of both root halves to 42C resulted in membrane damage that increased the loss of 14C-labeled photosynthates through leakage into the medium.
Knowledge of the level of soil temperatures that is detrimental for shoot and root growth for cool-season grasses may help develop heat-tolerant plants and effective management practices to improve summer performance. The objectives of this study were to determine the level and duration of high temperatures in the root zone that will induce decline for various growth and physiological parameters and to compare the responses of different physiological parameters and cultivars to high root-zone temperatures. Nine creeping bentgrass [Agrostis stolonifera L. var. palustris (Huds.) Farw.] cultivars were subjected to eight root-zone temperatures (20, 21, 22, 23, 25, 27, 31, 35 °C) in water baths while exposed to a constant air temperature of 20 °C for 54 days. Root number, dry weight, and depth, active root biomass, turf quality, leaf cytokinin content, and canopy net photosynthetic rate (Pn), decreased in all nine cultivars as root-zone temperature increased from 20 to 35 °C, but the time and temperature at which the decline occurred varied for each parameter measured. Pn, cytokinin content, root number, and turf quality declined at 23, 27, 27, and 35 °C, respectively, after 28 days of exposure. Active root biomass, root number, root dry weight, turf quality, and rooting depth declined at 23, 25, 25, 25, and 35 °C, respectively, at 54 days. At a 31 °C root-zone temperature the decline in root number, cytokinin content, and turf quality occurred at 19, 37, and 47 days, respectively. The results suggest that root-zone temperatures of 23 °C or above this level were detrimental to root activities, Pn, and overall turf growth. Root and Pn decline at lower temperatures and earlier in the study than turf quality suggest that the disturbance of physiological activities of roots and leaves could lead to turfgrass quality decline at high root-zone temperatures.
Turf quality of creeping bentgrass (Agrotis palustris L.) often declines during summer months. Reducing soil temperature alleviates bentgrass quality decline at supraoptimal air temperatures. The objective of this study was to investigate whether reducing soil temperature during the night is more effective than during the day in improving shoot and root growth when air temperature was supraoptimal for creeping bentgrass. The experiment was conducted in growth chambers using water baths to manipulate soil temperatures. Plants were exposed to the following temperature treatments: 1) optimal air and soil temperature during the day and night (20/20 °C, day/night, control); 2) high air and soil temperature during the day and night (35/35 °C, day/night); 3) lower soil temperatures during the day (20/35, 25/35, and 30/35 °C, day/night); and 4) lower soil temperature during the night (35/20, 35/25, and 35/30 °C) while air temperature was maintained at 35 °C during the day and night. Turf quality (on 1-9 scale) increased to the level of 6.5, 3.0, and 2.5 by reducing day soil temperature to 20, 25, or 30 °C, respectively, at 28 days of treatment, compared to the quality of 2.0 at 35/35 °C. Turf quality increased from 2.0 at 35/35 °C to 7.0, 6.0, and 4.5, respectively, by 28 days of exposure to night temperatures of 20, 25, and 30 °C. Chlorophyll content, root number, and root weight also were increased by reducing day or night soil temperature, and the increases were more pronounced for reduced night temperatures than day temperatures. These results demonstrated that reduced night soil temperature was more effective than reduced day soil temperature in improving shoot and root growth in creeping bentgrass under high air temperature conditions.
Growth of Magnolia grandiflora Hort. `St. Mary' (southern magnolia) trees in containers spaced 120 cm on center was studied for 2 years. During the 1st year, trees were grown in container volumes of 10, 27, or 57 liter. At the start of the second growing season, trees were transplanted according to six container shifting treatments [10-liter containers (LC) both years, 10 to 27LC, 10 to 57LC, 27LC both years, 27 to 57LC, or 57LC both years]. The mean maximum temperature at the center location was 4.8 and 6.3C lower for the 57LC than for the 27 and 10LC, respectively. Height and caliper, measured at the end of 2 years, were” greatest for magnolias grown continuously in 27 or 57LC. Caliper was greater for trees shifted from 10LC to the larger containers compared with trees grown in 10LC both years. Trees grown in 10LC both years tended to have fewer roots growing in tbe outer 4 cm of the growing medium at the eastern, southern, and western exposures. During June and August of the 2nd year, high air and growth medium temperatures may have been limiting factors to carbon assimilation. Maintenance of adequate carbon assimilation fluxes and tree growth, when container walls are exposed to solar radiation, may require increasing the container volume. This procedure may be more important when daily maximum air temperatures are lower during late spring or early fall than in midsummer, because low solar angles insolate part of the container surface.
( Vineland Research and Innovation Centre, 2013 ). Owing to the lack of well-adapted cultivars, garden rose sales have decreased from 25% to 30% during the past 20 years ( Byrne et al., 2010 ; Hutton, 2012 ; Pemberton and Karlik, 2015 ). Heat stress is one
experimental design. Iranian tall fescue ecotypes were subjected to the following three temperature treatments for 24 d. The treatments were 1) optimal temperatures, 2) heat stress, and 3) cold stress. In the first group, plants were maintained at optimal
Abstract
Direct heat injury to plant parts may occur in areas of high insolation and high humidity where transpiration is low. Using electrolyte leakage procedures, critical high temperatures of detached leaves of ‘Glen’ citrange [Citrus sinensis L. (Osbk.) × Poncirus trifoliata L. (Raf.)], ‘Swingle’ citrumelo [C. paradisi Macf. × P. trifoliata L. (Raf.)], and ‘Hamlin’ orange [C. sinensis L. (Osbk.)] were determined by exposure to temperatures between 25° and 65°C. Lethal temperatures for a 20 min exposure ranged from 54.3° ± 0.5° for ‘Glen’ citrange to 56.1° ± 0.4° for ‘Swingle’ citrumelo. Maximum canopy temperatures of 36.6° were recorded. Therefore, it appears that under field conditions in Florida, these cultivars are normally not subjected to temperatures that would cause direct heat injury.
We investigated the effects of evaporative cooling (EC), kaolin particle film (KP) and 20% shade net (SN) on the control of sunburn, fruit temperature amelioration and fruit quality of `Cripps' Pink' and `Royal Gala' apples [Malus domestica Borkh.] under orchard conditions during the 2003–04 season in Stellenbosch, South Africa. On days with maximum air temperatures of 34 to 37 °C, SN fruit were 5.4 to 9.7 °C cooler, EC fruit were 3.1 to 5.8 °C cooler and KP fruit were 1.5 to 6.4 °C cooler compared to the control (nontreated, CO) fruit. SN was effective in reducing fruit temperature from mid-morning until midafternoon; KP was most effective during late morning and early afternoon but not at midday; EC was effective from late morning on days when EC was activated. SN, followed by KP, was the most effective technique for controlling sunburn in fruit of both cultivars, with EC being less effective. The different technologies reduced fruit blush color compared to the CO treatment, with SN showing the most reduction and EC the least. EC increased fruit mass compared to all other treatments in `Royal Gala', and also increased fruit diameter and mass compared to CO in `Cripps' Pink'. We conclude that under the high radiation levels experienced in South African apple production areas, technologies which reduce irradiance as well as fruit temperature (KP, SN) are more effective in reducing sunburn than those which only reduce fruit temperature (EC). However, radiation-reducing technologies are potentially detrimental to color development on blushed apples.