scholarly journals Effect of Mulching to Root Zone Soil on Fruit Cracking, Plant Water Relation, and Fruit Growth and Quality in Sweet Cherry

2008 ◽  
Vol 7 (3) ◽  
pp. 351-358
Author(s):  
Takanori Yamamoto ◽  
Kohei Okuya ◽  
Hiroyuki Tanaka ◽  
Ko Kawakami ◽  
Akehiro Kanamoto
1979 ◽  
Vol 21 (4) ◽  
pp. 259-265 ◽  
Author(s):  
A. M. Ahmed ◽  
M. M. Heikal ◽  
M. A. Shaddad

2015 ◽  
Vol 35 (8) ◽  
Author(s):  
祝英 ZHU Ying ◽  
熊俊兰 XIONG Junlan ◽  
吕广超 LV Guangchao ◽  
Asfa Batool ASFA Batool ◽  
王兆滨 WANG Zhaobin ◽  
...  

2021 ◽  
Vol 8 (1) ◽  
Author(s):  
José Quero-García ◽  
Philippe Letourmy ◽  
José Antonio Campoy ◽  
Camille Branchereau ◽  
Svetoslav Malchev ◽  
...  

AbstractRain-induced fruit cracking is a major problem in sweet cherry cultivation. Basic research has been conducted to disentangle the physiological and mechanistic bases of this complex phenomenon, whereas genetic studies have lagged behind. The objective of this work was to disentangle the genetic determinism of rain-induced fruit cracking. We hypothesized that a large genetic variation would be revealed, by visual field observations conducted on mapping populations derived from well-contrasted cultivars for cracking tolerance. Three populations were evaluated over 7–8 years by estimating the proportion of cracked fruits for each genotype at maturity, at three different areas of the sweet cherry fruit: pistillar end, stem end, and fruit side. An original approach was adopted to integrate, within simple linear models, covariates potentially related to cracking, such as rainfall accumulation before harvest, fruit weight, and firmness. We found the first stable quantitative trait loci (QTLs) for cherry fruit cracking, explaining percentages of phenotypic variance above 20%, for each of these three types of cracking tolerance, in different linkage groups, confirming the high complexity of this trait. For these and other QTLs, further analyses suggested the existence of at least two-linked QTLs in each linkage group, some of which showed confidence intervals close to 5 cM. These promising results open the possibility of developing marker-assisted selection strategies to select cracking-tolerant sweet cherry cultivars. Further studies are needed to confirm the stability of the reported QTLs over different genetic backgrounds and environments and to narrow down the QTL confidence intervals, allowing the exploration of underlying candidate genes.


2021 ◽  
Vol 12 ◽  
Author(s):  
Shenglan Li ◽  
Liang Fang ◽  
Josefine Nymark Hegelund ◽  
Fulai Liu

Increasing atmospheric CO2 concentrations accompanied by abiotic stresses challenge food production worldwide. Elevated CO2 (e[CO2]) affects plant water relations via multiple mechanisms involving abscisic acid (ABA). Here, two tomato (Solanum lycopersicum) genotypes, Ailsa Craig (AC) and its ABA-deficient mutant (flacca), were used to investigate the responses of plant hydraulic conductance to e[CO2] and drought stress. Results showed that e[CO2] decreased transpiration rate (E) increased plant water use efficiency only in AC, whereas it increased daily plant water consumption and osmotic adjustment in both genotypes. Compared to growth at ambient [CO2], AC leaf and root hydraulic conductance (Kleaf and Kroot) decreased at e[CO2], which coincided with the transcriptional regulations of genes of plasma membrane intrinsic proteins (PIPs) and OPEN STOMATA 1 (OST1), and these effects were attenuated in flacca during soil drying. Severe drought stress could override the effects of e[CO2] on plant water relation characteristics. In both genotypes, drought stress resulted in decreased E, Kleaf, and Kroot accompanied by transcriptional responses of PIPs and OST1. However, under conditions combining e[CO2] and drought, some PIPs were not responsive to drought in AC, indicating that e[CO2] might disturb ABA-mediated drought responses. These results provide some new insights into mechanisms of plant hydraulic response to drought stress in a future CO2-enriched environment.


2013 ◽  
Vol 14 (2) ◽  
pp. 179
Author(s):  
Mirjana Stojanović ◽  
Dragan Milatović ◽  
Mirko Kulina ◽  
Zlatka Alić – Džanović

Susceptibility of 5 sweet cherry cultivars, grafted on Gisela 5, to rain induced fruit cracking was studied in the region of Sarajevo, during a two – year period (2010 – 2011). Testing of fruit cracking was done using index by Christensen. During the testing period, significant differences in susceptibility to fruit cracking among both the cultivars and the years of testing were found. All the cultivars had the highest fruit cracking index in 2010 year. The highest susceptibility to rain induced fruit cracking was evidenced in cultivar ‘Burlat’ during both years. Cultivars ‘Kordia’, ‘Regina’, ‘Karina’ and ‘Schneider's Spӓte Knorpelkirsche’ were moderately susceptible to fruit cracking.


2021 ◽  
pp. 282-303
Author(s):  
Lynn E. Long ◽  
Gregory A. Lang ◽  
Clive Kaiser

Abstract This chapter provides information on the processes that occur in the sweet cherry fruit during ripening prior to harvest. Some pre-harvest disorders, such as fruit cracking, and their management are presented. Some factors to consider during the harvesting of the fruits are also discussed, along with various harvesting techniques. Some postharvest fruit quality considerations are highlighted and the importance of postharvest temperature and humidity control and safe transport of fruits from the orchard to the packing house are pointed out.


2014 ◽  
pp. 477-488 ◽  
Author(s):  
C. Kaiser ◽  
E. Fallahi ◽  
M. Meland ◽  
L.E. Long ◽  
J.M. Christensen
Keyword(s):  

2004 ◽  
Vol 129 (3) ◽  
pp. 407-415 ◽  
Author(s):  
Matthew D. Whiting ◽  
Gregory A. Lang

Canopy fruit to leaf area ratios (fruit no./m2 leaf area, F:LA) of 7- and 8-year-old `Bing' sweet cherry (Prunus avium L.) on the dwarfing rootstock `Gisela 5' (P. cerasus L. × P. canescens L.) were manipulated by thinning dormant fruit buds. F:LA influenced yield, fruit quality, and vegetative growth, but there were no consistent effects on whole canopy net CO2 exchange rate (NCERcanopy). Trees thinned to 20 fruit/m2 LA had yield reduced by 68% but had increased fruit weight (+25%), firmness (+25%), soluble solids (+20%), and fruit diameter (+14%), compared to unthinned trees (84 fruit/m2). Fruit quality declined when canopy LA was ≈200 cm2/fruit, suggesting that photoassimilate capacity becomes limiting to fruit growth below this ratio. NCERcanopy and net assimilation varied seasonally, being highest during stage III of fruit development (64 days after full bloom, DAFB), and falling more than 50% by 90 DAFB. Final shoot length, LA/spur, and trunk expansion were related negatively to F:LA. F:LA did not affect subsequent floral bud induction per se, but the number of flowers initiated per bud was negatively and linearly related to F:LA. Although all trees were thinned to equal floral bud levels per spur for the year following initial treatment (2001), fruit yields were highest on the trees that previously had no fruit, reflecting the increased number of flowers initiated per floral bud. Nonfruiting trees exhibited a sigmoidal pattern of shoot growth and trunk expansion, whereas fruiting trees exhibited a double sigmoidal pattern due to a growth lag during Stage III of fruit development. Vegetative growth in the second year was not related to current or previous season F:LA. We estimate that the LA on a typical spur is only sufficient to support the full growth potential of a single fruit; more heavily-set spurs require supplemental LA from nonfruiting shoots. From these studies there appears to be a hierarchy of developmental sensitivity to high F:LA for above-ground organs in `Bing'/`Gisela 5' sweet cherry trees: trunk expansion > fruit soluble solids (Stage III) > fruit growth (Stage III) > LA/spur > shoot elongation > fruit growth (Stages I and II) > LA/shoot. Current season F:LA had a greater influence on fruit quality than prior cropping history, underscoring the importance of imposing annual strategies to balance fruit number with LA.


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