and Kourís-Lazos, 1996 ). Factors such as cultivar, weather and soil conditions, fruit ripeness, agronomic practices, and oil extraction process modify oil chemical composition and organoleptic characteristics ( García et al., 1996 ; Salvador et al
Ana Morales-Sillero, R. Jiménez, J.E. Fernández, A. Troncoso and G. Beltrán
Bao-Cheng Ma, Wan-Li Tang, Li-Yan Ma, Ling-Ling Li, Lu-Bin Zhang, Shi-Jiang Zhu, Chuxiong Zhuang and Donald Irving
and MeJA to determine the possible relationship between chitinase gene expression and resistance to anthracnose disease in harvested bananas during development from the green to the ripe stage. We also tested physical (heat) and chemical (H 2 O 2 - and
Mohsen Hatami, Siamak Kalantari, Forouzandeh Soltani and John C. Beaulieu
). The fruit mature ≈1 month after pollination and detach from the plant when ripe ( Hatami et al., 2016 ). The stripes change color as the fruit approaches maturity. The dark-green stripes become intense orange, maroon, or brown and the light
Charles E. Barrett, Xin Zhao, Charles A. Sims, Jeffrey K. Brecht, Eric Q. Dreyer and Zhifeng Gao
/BW, BW/MU, and BW/SU were harvested on 13 June and assessed after 4 d at the same ambient temperature. Fruit from the five field blocks were pooled for each treatment to provide enough ripe fruit for >100 sensory analysis samples. Tomatoes were cut from
P. Perkins-Veazie, J.K. Collins and S. Pair
The red flesh of watermelon contains the fat-soluble carotenoid pigment lycopene. A high level of lycopene in human blood serum has been correlated with a reduced incidence of several cancers. This experiment was done to determine the variation in lycopene content among watermelon cultivars and ripeness stages. Ten melons per cultivar of hybrid, open-pollinated, and triploid (seedless) types were selected from field plantings at Lane, Okla. Additionally, 20-melon, quarterly shipments of hybrid or triploid types were used from commercial growers. Melons were cut transversely and a 100-g sample of heart tissue was removed from the center, frozen at –80 °C, extracted with a hexane–acetone–ethanol mixture and pigment quantified at 503 nm. Unripe melons (about 3 to 5 days from fully ripe) had 18% less lycopene than ripe melons. The average lycopene content of all ripe melons sampled (open-pollinated, hybrid, triploid) was 47.82 μg/g (n = 247 melons), while that of ripe hybrid and triploid melons was 54.76 μg/g (n = 209 melons). Lycopene content of ripe melons varied among cultivars, from as little as 33.96 μg/g in `Crimson Sweet' to as much as 75.72 μg/g in `Scarlet Trio'. These results indicate that fresh watermelon has a naturally high level of lycopene and that potential for enhanced lycopene content is already present in the germplasm of commercial cultivars.
Tomato fruit transformed with the PG-antisense gene have been shown to exhibit persistent structural competence and extended shelf-life compared with normal, PG-containing lines. In this study, PG-antisense and nontransformed, wild-type fruit were examined for electrolyte efflux trends during ripening and following extended storage at the full-ripe stage. Pericarp disks from PG-antisense fruit showed minimal differences in net electrolyte efflux compared with the normal, wild-type fruit at the mature-green through ripe stages of development. Following extended storage (14 days) of ripe fruit, or in response to storage at chilling (1°C) temperatures, significantly higher (25%–33%) values for proportional electrolyte efflux were observed for wild-type fruit. Additionally, ripe wild-type fruit following extended storage or in response to chilling injury exhibited increased (15%–20%) total soluble electrolytes, particularly in tissues subjected to freeze-thaw versus thermal-disruption. Although PG-antisense fruit do exhibit increases in net electrolyte efflux during ripening, the enhanced efflux and electrolyte generation from wild-type ripe fruit during extended storage was due, in part, to the release of polyelectrolytes originating from pectin hydrolysis. These data may explain the divergence in postharvest performance and structural integrity of PG-antisense and normal, wild-type fruit during post-ripe storage and also suggest that modification of the apoplastic environment resulting from developmental increases in electrolyte efflux can enhance the catalytic activity of PG in vivo.
P. Perkins-Veazie, J.K. Collins, E. Baldwin and Fumi Takeda
Erect-fruited blackberries are often described as having a wild blackberry flavor. Flavor can be greatly affected by sugar and volatile composition, neither of which is known for erect-fruited blackberries. This study was done to characterize changes in sugar and volatile composition in ripening blackberries. Blackberries of `Navaho', `Arapaho', `Shawnee', and `Choctaw' were harvested at red, mottled, shiny, and dull black ripeness stages. Sucrose was found in small amounts (4% to 15%) in all stages of ripeness in all cultivars. Total sugars increased from ≈20–30 to 60–80 mg/g dry weight as fruit ripened from red to dull black. Fructose and glucose maintained a constant 1:1 ratio with ripeness stage and cultivar. Three of the four cultivars had a linear increase in total sugars with ripening; total sugars increased 4% to 40% as fruit ripened from shiny to dull black. Twenty to 25 volatile peaks were found by headspace gas chromatography in ripening blackberries. Six volatiles, tentatively identified as α-pinene, eugenol, limonene, p-cymene, α-terpinol, and gernaylacetone, appeared in all cultivars, but only in ripe (shiny and dull black) fruit. Few volatile peaks were observed in red (unripe) fruit. Data indicate that blackberries continue to increase in sugars in the latter stages of ripeness and that volatiles unique to ripe blackberries are produced during this period.
Wilhelmina Kalt, Christopher Lawand, Daniel A.J. Ryan, Jane E. McDonald, Horst Donner and Charles F. Forney
The antioxidant properties of blueberries have been examined only in ripe fruit, although fruit of different maturities are used in processed food products. In this study, highbush blueberry cultivars Bergitta, Bluegold, and Nelson highbush blueberry fruit at different stages of ripeness were examined to characterize differences in oxygen radical absorbing capacity (ORAC) and the phenolic components responsible for ORAC. Underripe fruit at different stages of maturity were also stored at 20 °C for up to 8 days to assess changes in ORAC and phenolic content. Anthocyanin content was substantially higher in fruit of more advanced stages of ripeness. In contrast, the phenolic content and ORAC were lower in the riper fruit. Anthocyanins continued to form during storage, although rate of pigment formation declined after about 4 days. Less anthocyanin pigment was formed in the less ripe fruit. After 8 days of storage, the anthocyanin content of fruit harvested 5% to 50% or 50% to 95% blue exceeded that of ripe fruit. Up to 60% of the total phenolic content could be accounted for by anthocyanins. ORAC was positively correlated with total phenolic content (R 2 = 0.78), but not with anthocyanin content.
Variability in maturity within a peach (Prunus persica, L. Batsch) fruit was estimated by measurements of force and the soluble solids concentration (SSC) at 16 coordinates around the peach at five maturity stages: 1) about one-half final swell (immature); 2) 85% final swell (green); 3) firm-ripe and similar to chip #3 of the Clemson Univ. system; 4) firm-ripe and similar to chip #5; and 5) tree-ripe. Firm-ripe 3 and 4 stages were firm enough to ship, but the tree-ripe stage was too soft. Firmness measured with a 4.7-mm-diameter penetrometer tip from two cultivars indicates a strong trend for the peach tip and cheeks to be firmer than tissue at other coordinates. Coordinates at the equator and around the stem end are generally firmer than coordinates at lat. 45°N, particularly in stages 3, 4, and 5. The SSC in juice from a cylinder of fruit adjacent to the puncture was higher at long. 90°E-W than at the sutures and higher at lat. 0° than at 70°S. Variance increased for force and decreased for SSC between maturity stages to the firm-ripe stage. The coordinate technique might be used to characterize and select cultivars that would be most suitable for once-over harvests.
Angela R. Davis, Charles L. Webber III, Wenge Liu, Penelope Perkins-Veazie, Amnon Levi and Stephen King
summer of 2007 and were harvested throughout the season. All full-sized fruit (n = 570) were weighed and then cut through the ground spot. Length and width were measured on approximately half the fruit harvested and was only measured on fully ripe fruit