Rain induced fruit cracking in sweet cherries takes 3 distinct forms: stem end cuticular fractures, calyx end cuticular fractures, and large cracks usually deep into the pulp on the cheek of the fruit. A 4-year study of sweet cherry varieties from a commercial orchard in Tasmania, Australia, was conducted to investigate the incidence of crack type and its relative likelihood, as influenced by both genotype and season. Although all 3 crack types developed in the 3-week period before commercial harvest, the extent of cracking was strongly controlled by season. While initial development of cracks coincided with rainfall, no relationship between amount of rain and incidence of cracking was found for crack type. A significant relationship was found between the tangential stress experienced by fruit skin from fruit at harvest maturity and the incidence of cracking recorded in the orchard. No other fruit property (pulp osmotic potential, fruit diameter, weight) explained the differences in incidence of cracking in the field between seasons or varieties. The results suggest that management of cracking needs to consider both varietal and seasonal factors. The development of turgor in maturing fruit also needs further investigation.
Salinity tolerance is a complex trait inferring the orchestrated regulation of a large number of physiological and biochemical processes at various levels of plant structural organisation. It remains to be answered which mechanisms and processes are crucial for salt tolerance in lucerne (Medicago sativa L.). In this study, salinity effects on plant growth characteristics, pigment and nutrient composition, PSII photochemistry, leaf sap osmolality, changes in anatomical and electrophysiological characteristics of leaf mesophyll, and net ion fluxes in roots of several lucerne genotypes were analysed. Salinity levels ranged from 40 to ~200 mm NaCl, and were applied to either 2-month-old plants or to germinating seedlings for a period of between 4 and 12 weeks in a series of hydroponic, pot and field experiments. Overall, the results suggest that different lucerne genotypes employ at least two different mechanisms for salt tolerance. Sodium exclusion appeared to be the mechanism employed by at least one of the tolerant genotypes (Ameristand 801S). This cultivar had the lowest leaf thickness, as well as the lowest concentration of Na+ in the leaf tissue. The other tolerant genotype, L33, had much thicker leaves and almost twice the leaf Na+ concentration of Ameristand. Both cultivars showed much less depolarisation of leaf membrane potential than the sensitive cultivars and, thus, had better K+ retention ability in both root and leaf tissues. The implications of the above measurements for screening lucerne germplasm for salt tolerance are discussed.
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