Fruit drop: The role of inner agents and environmental factors in the drop of flowers and fruits13-23.Views:371
The basic conditions of fruit set (synchronic bloom, transfer of pollen, etc.) still do decide definitely the fate of the flower (Cano-Medrano & Darnell, 1998) in spite of the best weather conditions (Stösser, 2002). Beyond a set quantity of fruits, the tree is unable to bring up larger load. A system of autoregulation works in the background and causes the drop of a fraction of fruits in spite of the accomplished fertilisation and the equality of physiological precedents (Soltész, 1997). There are also basically genetic agents in action. The further development of fruits maintained on the tree depends mainly on the growing conditions (e.g. water, supply of nutrients, weather adversities, pruning, fruit thinning, biotic damages, etc.), which may cause on their own turn fruit drop especially at the time of approaching maturity.
Physiological and biochemical evolution of peach leaf buds during dormancy course under two contrasted temperature patterns15-19.Views:104
Budbreak anomalies in temperate fruit trees grown under mild conditions have often been described. However, only few authors approached the physiological evolution of leaf buds all along the dormancy period according to the temperature pattern. The aim of this study was to characterize the evolution of peach leaf bud dormancy through some physiological and biochemical parameters under temperate winter conditions and under total cold deprivation after the endodormancy onset. Two treatments were applied in peach trees cv. Redhaven: (i) Regular Chilling Amounts — RCA and (ii) Total Chilling Deprivation — TCD. Buds were sampled periodically from different parts of the stem (terminal, medium and basal ones). We recorded the evolution of: carbohydrate concentrations (glucose, fructose, sucrose, sorbitol and starch), respiration rate, water contents and energy metabolism (ATP and ADP ratio). The dynamics of these parameters were compared and correlated with dormancy evolution ("one node cuttings" test) and budbreak patterns in plank:. The endodormancy intensity of terminal buds was significantly lower than those of median and basal buds in early October. Under RCA treatment, this gradient faded and the bud endodormancy release was completed at the same time in all positions along the stem. Thereafter, the "cuttings" test indicated that terminal buds grew slightly faster than median and basal buds, and, consistently, budbreak in planta started with the terminals buds, followed by the medians and then by the basal ones. The carbohydrate contents showed a transitory change only when the buds began to grow after the endodormancy was released under RCA. Respiration, water content and ATP/ADP changed dynamics only under RCA and only after the end of the endodormancy (their respective changes were very parallel). The dynamics of none of the tested parameters could be related with the endodormancy dynamics, but respiration, water content and ATP/ADP could be consistent markers of the actual bud growth before bud break (in this respect, ATP/ADP could not show differences between the terminal and axillary buds while respiration and water content could).
The increasing importance of grapevine trunk diseases21-30.Views:292
Grapevine trunk diseases (GTDs) are destroying the woody parts of the plants, resulting decline or dieback of the grapevine. More detailed research of the GTD began in 1950s, when Hewitt et al. (1957) observed that specific symptoms cannot be detected on the diseased trunks every year. Latest results have also proved that abiotic factors affect the appearance and the severity of the disease. Moreover several pathogenic fungi may play role as causative agents (Bertsch et al., 2013). Eutypa, Botryosphaeria, Phomopsis dieback, esca disease complex, and Petri disease are considered the major GTDs, where a variety of pathogens attack the woody perennial organs of the vine and ultimately lead to the death of the plant (Lehoczky, 1974; Larignon & Dubos, 1997; Rolshausen et al. 2010; Kotze et al., 2011; Bertsch et al., 2013; Fontaine et al., 2015).
The GTD incidence has been reported to be increased during the last decades (Úrbez-Torres et al., 2014). The esca incidence has reached 60% to 80% in some old vineyards in southern Italy (Pollastro et al., 2000; Surico et al., 2000; Calzarano & Di Marco, 2007). The disease incidence of the esca was reported to be increased from 1.83% to almost 13%, between 2003 and 2007 in Hungary (Dula, 2011). There was detected a five times increase in the GTD disease incidence in the Tokaj Wine Region, Hungary between 2014 and 2016 (Bihari et al,
Terminology of fruit set and fruit drop of sour cherry cultivars33-36.Views:186
Fruit set and fruit drop rates of 9 sour cherry cultivars (‘Érdi bôtermő’, ‘Debreceni bőtermő’, ‘Kántorjánosi’, ‘Újfehértói fürtös’, ‘Éva’, ‘Petri’ ‘Oblocsinszka’, ‘Pandy 279’ and ‘Csengôdi’) of eight years-old trees grown in Újfehértó, located in the Eastern north part of Hungary which grafted on Prunns mahaleb have been studied. Significant differences have been found in fruit set among cultivars. The average percentage of fruit set was 18.3%, which the ‘Oblacsinszka’ by 32.6% the highest fruit set, while ‘Debreceni bőtermő’ is very similar to ‘Pandy279’ showed lowest (12%) fruit set. Seasonal changes of fruit set and drop shows that there are four abscission peaks. The first fruit abortion wave appears during second week after pollination Thereafter, the second and third dropping period was found during the third and forth weeks after pollination. The forth abscission happened on the forth week after pollination. The highest fruit drop happened on ‘Pandy279’ (92.4%) very similar to ‘Éva’ (90%) while the lowest fruit drop observed in ‘Oblocsinszka’ (71.5%)
New sour cherry cultivars selected from local sources79-80.Views:260
New sour cherry cultivars selected from local sources