Rowland, Lisa J., Ogden, Elizabeth L., and Vinyard, Bryan T.
Agronomy; Aug2020, Vol. 10 Issue 8, p1067, 1p
Subjects
FRUIT development, FRUIT quality, BLUEBERRIES, PLANT development, PLANT populations, BUD development, HERITABILITY, and POLYPLOIDY
Abstract
A diploid blueberry mapping population, used previously to map quantitative trait loci (QTL) for chilling requirement and cold hardiness, was evaluated for several plant development and fruit quality traits. Specifically, the population was phenotyped in a greenhouse for timing of various stages of flower bud, leaf bud and fruit development and for fruit quality traits including weight, diameter, color, scar, firmness, flavor and soluble solids. Phenotypic data was analyzed statistically by analysis of variance, correlation tests, to examine associations of traits, and heritability. Results indicated that the traits were segregating and most were distributed normally in the population. Many of the development traits were correlated, and timing of shoot expansion, early bloom and full bloom was also correlated with the previously evaluated trait of chilling requirement. Some correlations were found among the fruit quality traits as well. For example, weight was highly correlated with diameter, and subjectively measured firmness was moderately correlated with one of the objectively measured firmness traits. In addition, most of the traits showed significant variation across genotypes and across years, and most had moderate to high heritability. Therefore, we conclude that the diploid population should be useful for identifying QTL for many of these traits. [ABSTRACT FROM AUTHOR]
FLOWERS, FRUIT research, BLUEBERRIES, CULTIVARS, and PLANT shoots
Abstract
Injury of open flowers often occurs in fruit crops by late winter or early spring frosts and can result in significant reduction in yield. In this study, freezing tolerance of open flowers of five highbush blueberry cultivars, Bluecrop, Elliott, Hannah's Choice, Murphy, and Weymouth, was determined using two freezing methods. Methods involved either placing whole plants in a radiation frost chamber or detached shoots in a glycol-freezing bath. In both methods, plants (or excised shoots) with opening flowers were exposed to temperatures ranging from -2 to -10 °C. After freeze treatments, several flower parts were evaluated for damage and the lethal temperature50 (LT50) determined. In order, from the most sensitive flower part to the least sensitive on average, were the corolla, filament, anther, style, exterior ovary, stigma, ovules, interior ovary, and placenta. A two-way analysis of variance (ANOVA) found no significant effect of the freezing method on the calculated freeze damage to most of the various flower parts. However, a significant genotype effect was found on freeze damage to the style, filament, anthers, and exterior ovary. Overall, 'Bluecrop' was the most sensitive to freezing, whereas 'Hannah's Choice' and 'Murphy' were the most freezing-tolerant. In conclusion, genotypic variability in frost tolerance of open highbush blueberry flowers was detected, which can be exploited in breeding for more frost-tolerant cultivars. [ABSTRACT FROM AUTHOR]
Ehlenfeldt, Mark K., Rowland, Lisa J., Ogden, Elizabeth L., and Vinyard, Bryan T.
Journal of the American Society for Horticultural Science. Jan2012, Vol. 137 Issue 1, p31-37. 7p.
Subjects
EFFECT of cold on plants, BLUEBERRIES, ACCLIMATIZATION (Plants), PLANT germplasm, and CLIMATE change
Abstract
Cold injury to plants can occur by early fall freezes before cold acclimation, by severe midwinter freezes that exceed the limits of the plant's tolerance, or by hard freezes in late winter or early spring after partial or complete deacclimation. Ideally, blueberry (Vaccinium L.) cultivars for temperate regions should acclimate to cold quickly in the fall, have a high midwinter-hardiness, and deacclimate late and/or slowly during spring or during unseasonably warm spells in winter, and do all of this without adversely delaying time of fruiting. Until recently, only limited evaluations have been done on the acclimation and deacclimation process in blueberry, although it is an integral part of flower bud survival and, thus, is directly related to potential yield. In this study, we have measured the timing and rate of acclimation and deacclimation in seven blueberry genotypes with different amounts of diverse species germplasm in their backgrounds. Primary differences observed among the seven genotypes were differences in maximum hardiness levels and the date at which they were reached, and differences in the date at which maximum acclimation levels were no longer sustained and deacclimation started. Highbush cultivars Bluecrop and Legacy (V. corymbosum L.), rabbiteye cultivar Tifblue [V. ashei Reade (= V. virgatum Aiton)], and two rabbiteye hybrid derivatives (US 1043 and US 1056) all reached maximum or near maximum cold-hardiness by late December with temperatures causing 50% lethality (LT50) in a range from -22 to -27 °C. The half-high, 'Northsky', and a hybrid of V. constablaei Gray × V. ashei 'Little Giant' both achieved cold acclimation of -28 °C or below (the lowest value we could measure) by the end of November. After reaching their maximum hardiness in late December, 'Legacy', 'Tifblue', and US 1043 began a sustained and relatively linear deacclimation, whereas US 1056, 'Bluecrop', 'Northsky', and 'Little Giant' sustained their acclimation for longer intervals. 'Bluecrop' and US 1056 did not begin to deacclimate until early March, and 'Little Giant' and 'Northsky' had no LT50 values higher (warmer) than -25 °C until late March. As concerns about climate change increase, knowledge of the ability of breeding germplasm to tolerate greater temperature extremes and fluctuations will prove increasingly valuable. [ABSTRACT FROM AUTHOR]
