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Bermudagrass (Cynodon spp.) turf is often overseeded with a cool-season species such as perennial ryegrass (Lolium perenne L.) to provide an improved winter surface for activities such as golf or athletic events. Perennial ryegrass can become a persistent weed in overseeded turf due to the heat and disease tolerance of improved cultivars. Intermediate ryegrass is a relatively new turfgrass that is a hybrid between perennial and annual ryegrass (L. multiflorum Lam.). Very little information is available on intermediate ryegrass as an overseeding turf. Greenhouse, field, and growth chamber studies were designed to compare two cultivars of intermediate ryegrass (`Transist' and `Froghair') with three cultivars of perennial ryegrass (`Jiffie', `Racer', and `Calypso II') and two cultivars of annual ryegrass (`Gulf' and `TAM-90'). In a greenhouse study, the perennial ryegrass cultivars had finer leaf texture (2.9-3.2 mm), shorter collar height (24.7-57.0 mm), and lower weight/tiller (29-39 mg) than the intermediate and annual cultivars. In the field studies, the intermediate cultivar Transist exhibited improved turfgrass quality (6.1-7.1) over the annual cultivars (4.5-5.8) and the other intermediate cultivar Froghair (5.4-5.7). However, neither of the intermediate cultivars had quality equal to the perennial ryegrass cultivars (7.0-7.9). The perennial ryegrass cultivars exhibited slow transition back to the bermudagrass compared to the annual and intermediate ryegrass cultivars. In the growth chamber study, the annual and intermediate cultivars all showed increased high-temperature stress under increasing temperatures compared to the perennial cultivars, which did not show stress until air temperature exceeded 40 °C. Collectively, these studies indicate that the intermediate ryegrass cultivar Transist may have promise as an overseeding turfgrass due to its improved quality compared to annual types and a lack of heat tolerance relative to perennial cultivars, but with transition qualities similar to perennial ryegrass.

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Seedlings of six provenances of Atlantic white cedar [Chamaecyparis thyoides (L.) B.S.P.] (Escambia Co., Ala., Santa Rosa Co., Fla., Wayne Co., N.C., Burlington Co., N.J., New London Co., Conn., and Barnstable Co., Mass.) were grown in controlled-environment chambers for 12 weeks under 16-hour photoperiods with 16-hour days/8-hour nights of 22/18 °C, 26/22 °C, 30/26 °C, 34/30 °C or 38/34 °C. Considerable variation in height, foliage color, and overall plant size was observed among plants from the various provenances. Seedlings from the two most northern provenances (Massachusetts and Connecticut) were most heat sensitive as indicated by decreasing growth rates at temperature regimes >22/18 °C. In contrast, plants from New Jersey and the three southern provenances (North Carolina, Florida, and Alabama) exhibited greater heat tolerance as indicated by steady or increasing growth rates and greater top and root dry weights as temperature regimes increased above 22/18 °C. Growth rates of seedlings from the four aforementioned provenances decreased rapidly at temperature regimes >30/26 °C suggesting low species tolerance to high temperatures. There were no significant differences in seedling dry matter production among provenances when temperature regimes were ≥34/30 °C. Net shoot photosynthesis and dark respiration of plants did not vary by provenance; however, net photosynthesis was temperature sensitive and decreased at temperature regimes >26/22 °C. Foliar respiration rates increased as temperature increased from 22/18 °C to 26/22 °C, but then remained relatively constant or decreased at higher temperature regimes. Plants at temperatures ≥34/30 °C exhibited severe stunting, chlorosis, and necrosis on branch tips. However, tissue concentrations of N, P, K, Ca, Mg, Fe, Zn, Cu, and Mn generally increased with temperature regimes >30/26 °C indicating that mineral nutrient concentration was not a limiting factor at high temperatures.

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, which may negatively impact the agricultural production and food availability ( Karl and Trenberth, 2003 ; Wurr et al., 1996 ). Heat tolerance is the ability of plants to grow and perform well under high temperature stress. Development of new crop

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Greenhouse-cultured, container-grown seedlings of interior Douglas fir [Pseudotsuga menziesii var. glauca (Beissn.) France], Engelmann spruce [Picea engelmannii (Parry) Engelm.], and ponderosa pine (Pinus ponderosa var. scopulorum Engelm.) were acclimated and deacclimated to cold in growth chambers over 19 weeks. Heat tolerance and cold hardiness of needles, and bud dormancy, were measured weekly. Heat tolerance of Douglas fir and Engelmann spruce needles increased with development through the first complete annual cycle: new needles on actively growing plants; mature needles, not cold-hardy, on dormant plants; cold-hardy needles on dormant and quiescent plants; and mature, needles, not cold-hardy, on actively growing plants. Heat tolerance of ponderosa pine needles differed in two respects. New needles had an intermediate tolerance level to heat, and fully cold-hardy needles were the least tolerant. Thus, the physiological changes that conferred cold hardiness were not associated with greater heat tolerance in all the conifers tested. In none of these species did the timing of changes in heat tolerance coincide consistently with changes in cold hardiness or bud dormancy.

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Abstract

Inheritance and selection of heat tolerance were investigated in common bean (Phaseolus vulgaris L.). Parental, F1, backcross, and F2 populations from the crosses PI 271998 × BBL 47, PI 271998 × 80 BP-6 and 5BP-7 × BBL 47 were used in the inheritance study. Parental, F2, F3 and backcross populations of the cross PI 271998 × BBL 47 were used to estimate selection gain. Plants were evaluated for heat tolerance by the conductivity method after 32 days in the growth chamber at 20°/15°C (day/night) and acclimation at 37° for 24 hr. The joint scaling test indicated that the additive-dominance model was adequate to explain heat tolerance in crosses PI 271998 × BBL 47 and 5BP-7 × BBL 47. The major variation for tolerance for these 2 crosses may be controlled by a small number of genes. The additive-dominance model was inadequate for PI 271998 × 80BP-6, however, and epistasis was present. Narrow sense heritability estimates ranged from 2.9% to 24.0%, indicating relatively small additive effects. Broad sense heritability estimates ranged from 0.0% to 21.6%, suggesting sizable environmental effects. Realized heritability from selection for tolerant F2 plants was 7.9%. These estimates perhaps represent the lower limit of heritability for heat tolerance. The conductivity method could be considered for evaluating heat tolerance in a breeding program but should be more effective in screening F3 families than individual F2 plants.

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Abstract

Several tuber-bearing Solanum species with different levels of frost hardiness and different capacities for cold acclimation were studied for the interrelationship of freezing and heat tolerance after cold and heat acclimation. Cold acclimation could increase the frost hardiness in some species as previously reported, but except for S. commersonii it did not change the heat hardiness in species studied. Heat acclimation, on the other hand, could increase the heat hardiness in all tested species without affecting their frost hardiness. There is no systematic relationship between freezing and heat tolerance and no correlation in heat hardiness between the controls and the heat acclimated plants. The results indicate that the mechanisms of cold and heat acclimation in the potato appear to be independent of each other.

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The genetic basis for heat tolerance during reproductive development in snap bean was investigated in a heat-tolerant × heat-sensitive common bean cross. Parental, F1, F2, and backcross generations of a cross between the heat-tolerant snap bean breeding line `Cornell 503' and the heat-sensitive wax bean cultivar Majestic were grown in a high-temperature controlled environment (32 °C day/28 °C night), initiated prior to anthesis and continued through plant senescence. During flowering, individual plants of all generations were visually rated and scored for extent of abscission of reproductive organs. The distribution of abscission scores in segregating generations (F2 and backcrosses) indicated that a high rate of abscission in response to heat stress was controlled by a single recessive gene from `Majestic'. Abscission of reproductive organs is the primary determinant of yield under heat stress in many annual grain legumes; this is the first known report of single gene control of this reaction in common bean or similar legumes. Generation means analysis indicated that genetic variation among generations for pod number under heat stress was best explained by a six-parameter model that includes nonallelic interaction terms, perhaps the result of the hypothetical abscission gene interacting with other genes for pod number in the populations. A simple additive/dominance model accounted for genetic variance for seeds per pod. Dominance [h] and epistatic dominance × dominance [l] genetic parameters for yield components under high temperatures were the largest in magnitude. Results suggest `Cornell 503' can improve heat tolerance in sensitive cultivars, and heat tolerance in common bean may be influenced by major genes.

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Abstract

Two laboratory techniques for estimating genotypic differences in response to heat stress—the electrical conductivity and the 2,3,5-triphenyl tetrazolium chloride reduction tests—were compared in tests with 26 cultivars of beans (Phaseolus vulgaris L.) previously evaluated for heat tolerance. After heat acclimation of plants, leaf disks were subjected to heat stress over a range of temperatures. The temperature causing 50% injury above the control, considered as the killing temperature, was estimated by fitting the data to a sigmoidal model. Although cultivar killing temperatures were correlated between tests, only killing temperatures for the conductivity test were correlated with yield performance under stress in the field.

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Four heat-tolerant (`Celebration Cherry Red', `Celebration Rose', `Lasting Impressions Shadow', and `Paradise Moorea') and three non-heat-tolerant (`Lasting Impressions Twilight', `Danziger Blues', and `Pure Beauty Prepona') cultivars were identified using a Weighted Base Selection Index. These cultivars were used as parents in a full diallel crossing block with reciprocals and selfs. Progeny from five parents (25 crosses) were evaluated for heat tolerance. Four floral (fl ower number, flower diameter, flower bud number, and floral dry weight) and five vegetative characteristics (visual rating, leaf size rating, vegetative dry weight, branch number, and node number) were evaluated with emphasis placed on continued flowering under long-term heat stress. In addition, progeny from all seven parents (49 crosses) were evaluated for inheritance of adaxial leaf color, abaxial leaf color, vein color, and flower color. Significant differences were found in each data category (P < 0.001) with the exception of node number, which was not significant. Flower number varied from 0 to 2, flower diameter varied from 0 to 41 mm, floral dry weight varied from 14 to 105 mg, bud number varied from 0 to 12, branch number varied from 5 to 15, and vegetative dry weight varied from 220 to 607 mg. General and specific combining abilities of the parents were evaluated as was heritability. It was found that the four heat-tolerant cultivars had higher general combining abilities. Heat tolerance has low heritability and is controlled by many genes.

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Red-osier dogwood sterns, Cornus sericea L., at ten different growth stages were subjected to a series of temperatures ranging from 25C to 60C by immersing them in a water bath for one hour. After heat treatments, the viability of internode tissues were determined by electrical conductivity and ethylene production. Heat tolerance was expressed as LT50, the temperature at which 50% of the tissues were injured. The results suggest that the LT50 of dormant plants remained relatively constant, approximately 53C. During dormancy, heat stress did not stimulate ethylene production from internode tissues. In contrast, tissues from non-dormant plants exposed to heat stress produced increasing levels of ethylene reaching a peak at 40C followed by a steady decrease at higher temperatures. Application of 1-aminocyclopropane-1-carboxylic acid (ACC) to stem segments from dormant plants, following heat treatment, enhanced production of ethylene.

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