No abstract

Green 'Anjou' pear and its bud mutation, red 'Anjou' were compared to understand their differences in phenolic metabolism and its effect on primary metabolism. In the flesh of the two cultivars, no difference was detected in the concentration of any phenolic compound, the transcript level of MYB10 or the transcript levels or activities of key enzymes involved in anthocyanin synthesis. Compared with green 'Anjou', the shaded peel of red 'Anjou' had higher anthocyanin concentrations, higher transcript levels of MYB10 and higher activity of UDP-glucose:flavonoid 3-O-glycosyltransferase (UFGT), suggesting that MYB10 regulates UFGT to control anthocyanin synthesis in red 'Anjou' peel. In the sun-exposed peel, activities of phenylalanine ammonia lyase, dihydroflavonol reductase, flavonol synthase and anthocyanidin synthase as well as UFGT were higher in red 'Anjou' than in green 'Anjou'. The peel of red 'Anjou' had higher activities of sorbitol dehydrogenase, raffinose synthase and sucrose synthase and higher levels of raffinose, myo-inositol and starch, indicating that sorbitol metabolism, raffinose synthesis and starch synthesis were upregulated in red 'Anjou'. The flesh of red 'Anjou' had higher concentrations of glucose, but lower activities of ATP-dependent phosphofructokinase, pyruvate kinase and glucose-6-phosphate dehydrogenase and lower dark respiration. The peel of red 'Anjou' had higher activities of glutaminase, asparagine synthetase and asparaginase, and higher concentrations of asparagine, aspartate, alanine, valine, threonine and isoleucine. The effects of anthocyanin synthesis on primary metabolism in fruit peel are discussed.

Sweet cherry (Prunus avium L.) producers in the Pacific Northwest have devoted considerable acreage to late-maturing cultivars. By using these cultivars to extend the harvest window, producers avoid lower returns associated with cherries harvested during the peak period (i.e., midseason) when supplies are overly abundant. Over several years, we evaluated preharvest applications of gibberellic acid (GA3) between 10 and 100 ppm (a.i.) on the late-maturing sweet cherry cultivars Lapins, Skeena, Staccato, and Sweetheart. Individual trials examined the timing of GA3 applications and/or rate on fruit quality attributes at harvest and after 4 weeks of cold storage at 0 °C. The influence of GA3 timing and/or rate on sweet cherry skin color and harvest delay was also evaluated. Multiple applications split between the end of Stage II (pit hardening) and mid-Stage III (final fruit swell) of fruit development did not improve fruit quality attributes or delay skin color development of ‘Skeena’ and ‘Sweetheart’ compared with equivalent concentrations applied once at the end of Stage II. Low concentrations (between 10 and 25 ppm) consistently improved fruit firmness (FF) of all cultivars by 10% to 43%. No further improvements in FF were observed when rates exceeded 25 ppm. Skin color development was retarded by GA3 but did not respond in a consistent manner to increasing rate. Fruit size was not uniformly increased by GA3. In trials where GA3 had a positive effect on fruit size, the effect was observed at low concentrations and was not further improved with increasing rate. A cultivar-dependent response to GA3 was observed for return bloom. ‘Skeena’ reproductive buds per fruiting spur and flowers per floral bud in years after treatment were unaffected by GA3 concentration. On the contrary, the number of flowers per bud of ‘Lapins’ was significantly reduced to 79% and 38% of control levels for 50 and 100 ppm GA3, respectively. At 100 ppm, GA3 additionally limited the number of reproductive buds returning on fruiting spurs of ‘Lapins’. GA3 reduced stem browning and surface pitting disorder of ‘Sweetheart’ and ‘Lapins’ after 4 weeks of cold storage at 0 °C; however, these effects were optimized at 25 ppm. Respiration rate and weight loss were unaffected by GA3 at harvest or after 2 and 4 weeks of cold storage. Unidentified endogenous factors that regulate FF and are inducible by GA3 appear to be largely responsible for improved resistance to pitting. Collectively, the results demonstrate high sensitivity of cherry FF and skin color to GA3. Split applications did not provide further harvest delays or affect any of the attributes evaluated, possibly because low rates (20 ppm) applied at the first timing were sufficient to saturate the response. In general, fruit quality of late-maturing cultivars of sweet cherry was improved by low rates of GA3 applied in a single application at the end of pit hardening.

European pears (Pyrus communis L.) require a range of cold-temperature exposure to induce ethylene biosynthesis and fruit ripening. Physiological and hormonal responses to cold temperature storage in pear have been well characterized, but the molecular underpinnings of these phenomena remain unclear. An established low-temperature conditioning model was used to induce ripening of ‘D’Anjou’ and ‘Bartlett’ pear cultivars and quantify the expression of key genes representing ripening-related metabolic pathways in comparison to non-conditioned fruit. Physiological indicators of pear ripening were recorded, and fruit peel tissue sampled in parallel, during the cold-conditioning and ripening time-course experiment to correlate gene expression to ontogeny. Two complementary approaches, Nonparametric Multi-Dimensional Scaling and efficiency-corrected 2-(ΔΔCt), were used to identify genes exhibiting the most variability in expression. Interestingly, the enhanced alternative oxidase (AOX) transcript abundance at the pre-climacteric stage in ‘Bartlett’ and ‘D’Anjou’ at the peak of the conditioning treatments suggests that AOX may play a key and a novel role in the achievement of ripening competency. There were indications that cold-sensing and signaling elements from ABA and auxin pathways modulate the S1-S2 ethylene transition in European pears, and that the S1-S2 ethylene biosynthesis transition is more pronounced in ‘Bartlett’ as compared to ‘D’Anjou’ pear. This information has implications in preventing post-harvest losses of this important crop.

Reflective fabric was installed before bloom in 2009 and 2010 in alleyways of a mature, low-density ‘Anjou’ pear orchard (269 trees/ha). Four treatments were applied to study intracanopy light environments on fruit growth rate and size, cropload, yield, and fruit quality: 1) no fabric (NF); 2) partial-season fabric applied before full bloom (FB) and removed 75 days after full bloom (dafb) (PSF); 3) full-season fabric applied before FB and removed at harvest (FSF); and 4) shadecloth (60%) applied 60 dafb through harvest (SC). PSF and FSF improved yield by 12% and 18%, respectively, over the two-year period relative to NF. The high yields of fabric treatments were attributed to fruit number in the lower (less than 2.4 m) interior, mid-, and exterior zones of the canopy. Photosynthetic active radiation (PAR) was increased by fabric 28%, 95%, and 30% in the lower exterior, mid-, and interior canopy, respectively. Photosynthesis:light response curves indicated improved carbon assimilation of pear leaves developing in the elevated PAR environment of the lower canopy. Fruit growth rate and final size were unaffected by fabric treatments. FSF fruit size was similar to NF despite higher fruit density. Compared with NF, FSF had a small, non-significant effect on fruit maturity (increased softening) at harvest. Yield and fruit size of SC fruit were significantly reduced. The number of fruit in SC trees did not differ from NF in 2009, but the effect of shade reduced fruit number in 2010. Fabric did not affect fruit quality attributes after three and six months of regular atmosphere cold storage. Pears from SC trees did not attain ripening capacity after three months of cold storage and a 7-day ripening period and had lower sugar content compared with other treatments. The cumulative yield advantages associated with FSF support its use in mature pear orchards.