scholarly journals Differences in Fruit Development among Large- and Small-fruited Cultivars of Saskatoon (Amelanchier alnifolia)

2001 ◽  
Vol 126 (4) ◽  
pp. 381-385 ◽  
Author(s):  
Roisin McGarry ◽  
Jocelyn A. Ozga ◽  
Dennis M. Reinecke
Keyword(s):  
Fruit Development ◽  
Developmental Stages ◽  
Fruit Size ◽  
Cell Number ◽  
Fruit Growth ◽  
Stage I ◽  
Canadian Prairies ◽  
Amelanchier Alnifolia ◽  
Minimum Number ◽  
Harvest Maturity

Fruit growth in saskatoons (Amelanchier alnifolia Nutt.), an emerging horticultural crop across the Canadian prairies, results from development of the mesocarp and the endocarp-locular-ovular structure which includes the developing seeds. Contribution of these tissues to fruit size was assessed using transverse sections of ovaries sampled at six developmental stages among large- and small-fruited cultivars. Mesocarp development was similar among the larger-fruited cultivars (Thiessen, Northline, and Smoky); the number of cells increased rapidly through Stage I [162 to 293 growing degree days (GDDs)] of fruit growth, and cell number increase was minimal during Stages II (293 to 577 GDDs) and III (577 to 747 GDDs). In `Regent' fruit (a small-fruited cultivar), the maximal rate of cell division was delayed until Stage II and the mesocarp contained fewer cells than the larger-fruited cultivars at harvest maturity. Mesocarp cell enlargement was similar among all of the cultivars studied where cell expansion was maximal during Stage I and continued at a slower rate during Stages II and III. The area of the endocarp-locular-ovular structure was greatest for `Thiessen' and `Northline', midrange for `Smoky', and smallest for `Regent'. Data suggest that a minimum number of mesocarp cells early in fruit development is required to attain maximal mesocarp size, and that differences in cultivar fruit size are a function of both the mesocarp and the endocarp-locular-ovular structure.

scholarly journals Fruit Development in Saskatoon (Amelanchier alnifolia Nutt.)

HortScience ◽  
1996 ◽  
Vol 31 (4) ◽  
pp. 682f-682
Author(s):  
Roisin McGarry ◽  
Jocelyn A. Ozga ◽  
Dennis M. Reinecke
Keyword(s):  
Fruit Development ◽  
Fruit Size ◽  
Fruit Weight ◽  
Growth Patterns ◽  
Fruit Growth ◽  
Seed Number ◽  
Fresh Weight ◽  
Canadian Prairies ◽  
Developmental Patterns ◽  
Growing Seasons

Saskatoon fruits, an emerging horticultural crop across the Canadian prairies, vary greatly in size among cultivars. In this study, we compare fruit development patterns among large, medium, and small fruited cultivars of saskatoon, and assess the role of seed number and pedicel diameter on fruit size. Fruit growth patterns of four cultivars (Thiessen, Northline, Regent, and Smoky) were determined from weekly measurements of fruit diameters and fresh and dry flower/fruit weights during two consecutive growing seasons. The developmental patterns of fruit growth determined using the above criteria were similar among cultivars and between years. At maturity, the largest fruits (fresh weight) obtained were from cv. Thiessen, followed by `Northline', `Smoky', and `Regent', in descending order. Pedicel diameters (one week prior to maturity) correlated linearly with increasing fruit diameter and fresh weight. At maturity, seed number per fruit correlated linearly with increasing fruit weight. Thiessen contained significantly more seeds per fruit (4.6) than `Northline' (3.7), `Smoky' (3.2), and `Regent' (3.2).

scholarly journals Rootstock Effects on Growth, Cell Number, and Cell Size of `Gala' Apples

2004 ◽  
Vol 129 (1) ◽  
pp. 37-41 ◽  
Author(s):  
Yahya K. Al-Hinai ◽  
Teryl R. Roper
Keyword(s):  
Cell Division ◽  
Cell Size ◽  
Agricultural Research ◽  
Fruit Size ◽  
Cell Number ◽  
Fruit Growth ◽  
Research Station ◽  
Full Bloom ◽  
Final Size ◽  
Load Effects

The effects of rootstock on growth of fruit cell number and size of `Gala' apple trees (Malus domestica Borkh) were investigated over three consecutive seasons (2000-02) growing on Malling 26 (M.26), Ottawa-3, Pajam-1, and Vineland (V)-605 rootstocks at the Peninsular Agricultural Research Station near Sturgeon Bay, WI. Fruit growth as a function of cell division and expansion was monitored from full bloom until harvest using scanning electron microscopy (SEM). Cell count and cell size measurements showed that rootstock had no affect on fruit growth and final size even when crop load effects were removed. Cell division ceased about 5 to 6 weeks after full bloom (WAFB) followed by cell expansion. Fruit size was positively correlated (r2 = 0.85) with cell size, suggesting that differences in fruit size were primarily a result of changes in cell size rather than cell number or intercellular space (IS).

scholarly journals Association between Fruit Development and Mature Fruit Drop in Huanglongbing-affected Sweet Orange

HortScience ◽  
2020 ◽  
Vol 55 (6) ◽  
pp. 851-857
Author(s):  
Lisa Tang ◽  
Sukhdeep Singh ◽  
Tripti Vashisth
Keyword(s):  
Fruit Development ◽  
Sweet Orange ◽  
Water Status ◽  
Fruit Size ◽  
Substantial Reduction ◽  
Fruit Growth ◽  
Mature Fruit ◽  
Callose Deposition ◽  
Immature Fruit ◽  
Fruit Drop

In the past decade, FL citrus industry has been struck by Huanglongbing (HLB), a disease caused by the phloem-limited bacterium Candidatus Liberibacter asiaticus (CLas). Besides tree decline, HLB causes a sharp increase in mature fruit drop before harvest, leading to a substantial reduction in citrus production. The aim of the study was to provide insights in HLB-associated mature fruit drop. For HLB-affected ‘Valencia’ and ‘Hamlin’ sweet orange (Citrus sinensis), trees exhibiting severe symptoms (“severe trees”) had a significantly higher rate of mature fruit drop compared with mildly symptomatic ones (“mild trees”). Interestingly, dropped fruit were smaller than those still attached to tree branches regardless of the symptom levels of trees; overall, fruit of severe trees were smaller than mild trees. The result suggests a negative effect of HLB on fruit growth that may lead to a high incidence to drop subsequently at maturity. This possibility is further supported by the difference in immature fruit size as early as 2 months after bloom between severe and mild trees. Although HLB-triggered phloem plugging due to callose deposition in citrus leaves, which results in disrupted carbohydrate transport, has been documented in literature, the results of the histological analysis demonstrated no consistent pattern of callose deposition in the mature fruit pedicel in relation to the drop incidence. Additionally, sugar concentration in juice was not significantly different between dropped and attached fruit, providing evidence that carbohydrate shortage is not the case for dropped fruit and thus not the predominant cause of HLB-associated mature fruit drop. Notably, the midday water potential was significantly lower for severe than mild trees during the preharvest period (2 weeks before harvest of the current crop) in late March, which was also the second week after full bloom of return flowering. This suggests that altered tree water status due to HLB might limit fruit growth during the initial stage of fruit development (immediately after flowering) and/or increase the incidence of mature fruit abscission, leading to elevated preharvest fruit drop. Together, the results suggest that in the presence of HLB, strategies to increase fruit size and minimize additional stresses (especially drought) for the trees may improve mature fruit retention.

scholarly journals Response of Cell Division and Cell Expansion to Local Fruit Heating in Tomato Fruit

2012 ◽  
Vol 137 (5) ◽  
pp. 294-301 ◽  
Author(s):  
Julienne Fanwoua ◽  
Pieter de Visser ◽  
Ep Heuvelink ◽  
Gerco Angenent ◽  
Xinyou Yin ◽  
...  
Keyword(s):  
Cell Expansion ◽  
Tomato Fruit ◽  
Fruit Size ◽  
Growth Period ◽  
Cell Number ◽  
Fruit Growth ◽  
Growth Responses ◽  
Direction Parallel ◽  
Cell Divisions ◽  
Fruit Skin

To improve our understanding of fruit growth responses to temperature, it is important to analyze temperature effects on underlying fruit cellular processes. This study aimed at analyzing the response of tomato (Solanum lycopersicum) fruit size to heating as affected by changes in cell number and cell expansion in different directions. Individual trusses were enclosed into cuvettes and heating was applied either only during the first 7 days after anthesis (DAA), from 7 DAA until fruit maturity (breaker stage), or both. Fruit size and histological characteristics in the pericarp were measured. Heating fruit shortened fruit growth period and reduced final fruit size. Reduction in final fruit size of early-heated fruit was mainly associated with reduction in final pericarp cell volume. Early heating increased the number of cell layers in the pericarp but did not affect the total number of pericarp cells. These results indicate that in the tomato pericarp, periclinal cell divisions respond differently to temperature than anticlinal or randomly oriented cell divisions. Late heating only decreased pericarp thickness significantly. Continuously heating fruit reduced anticlinal cell expansion (direction perpendicular to fruit skin) more than periclinal cell expansion (direction parallel to fruit skin). This study emphasizes the need to measure cell expansion in more than one dimension in histological studies of fruit.

scholarly journals 745 PB 079 SINK SIZE IN GAs-TREATED AND POLLINATED RABBITEYE BLUEBERRY FRUITS

HortScience ◽  
1994 ◽  
Vol 29 (5) ◽  
pp. 539g-539
Author(s):  
Raouel Cano-Medrano ◽  
Rebecca L. Darnell
Keyword(s):  
Cell Size ◽  
Fruit Set ◽  
Fruit Size ◽  
Cell Number ◽  
Cross Sectional Area ◽  
Stage I ◽  
Stage Ii ◽  
Sectional Area ◽  
Cross Sectional ◽  
Small Fruit

Exogenous applications of GA, have induced pathenocarpic fruit set in blueberry; however, size of GA,-treated fruit is smaller than pollinated fruit. The small fruit size in GA3-treated fruit may be related to either cell number and/or cell size. Thus, these parameters were examined throughout development in pollinated, non-pollinated and GA3-treated fruits. Fruit growth followed a double sigmoid pattern. During Stage I (0-25 DAA), fruit size in GA,-treated, pollinated, and non-pollinated fruits averaged 0.33, 0.39, and 0.16 g, respectively. There was little change in fruit size in Stage II (25-45 DAA). At ripening, fruit size averaged 1.7 g for GA,-treated and 2.6 g for pollinated fruits. Non-pollinated fruit abscised in Stage II. At anthesis, mesocarp cell number averaged 9910 cells per median cross sectional area and remained constant up to ripening. In Stage I, cell size in G A3-treated and pollinated fruits increased 7X and 9X respectively. Cell size in both fruit types increased 1.5X and 2.8X during Stage II and Stage 111, respectively. Fruit cell number was set at anthesis and differences in fruit size were due to differences in cell ellongation in Stage I.

scholarly journals Calcium Absorption during Fruit Development in ‘Honeycrisp’ Apple Measured Using 44Ca as a Stable Isotope Tracer

HortScience ◽  
2017 ◽  
Vol 52 (12) ◽  
pp. 1804-1809 ◽  
Author(s):  
Lee Kalcsits ◽  
Gregory van der Heijden ◽  
Michelle Reid ◽  
Katie Mullin
Keyword(s):  
Stable Isotope ◽  
Fruit Development ◽  
Developmental Stages ◽  
Calcium Absorption ◽  
Fruit Size ◽  
Absorption Efficiency ◽  
Stable Isotope Tracer ◽  
Isotope Tracer ◽  
Bitter Pit ◽  
Balance Analysis

Calcium (Ca) sprays are commonly used to control Ca-related disorders such as bitter pit in apple. Increases in the frequency and the amount of Ca applied directly to the fruit have increased fruit Ca levels and are associated with a reduction in bitter pit incidence. However, the absorption efficiency at different fruit developmental stages is poorly understood. Here, the absorption efficiency was measured using 44Ca stable isotope applied to 30 individual fruit at five different times every 2 weeks between June drop and 2 weeks before harvest in a medium-density ‘Honeycrisp’ orchard. Fruit size, spray adhesion, and Ca and potassium (K) content were monitored weekly for 12 weeks between 26 May and 13 Aug. 2015. At harvest, the 44Ca-labeled fruit was picked and separated into peel and inner fruit for mass balance analysis of 44Ca absorption to regions of the fruit that are important to prevent Ca-related disorders. As expected, δ44Ca was greater in the peel than the interior of the fruit. However, there was a significant amount of 44Ca present in the inner fruit at harvest for all five applications applied during the growing season. Using a stable isotope tracer approach, we present evidence that Ca is absorbed throughout fruit development. These findings support current recommendations for frequent Ca applications in low concentrations throughout fruit development to increase fruit Ca levels and reduce the incidence of bitter pit in ‘Honeycrisp’ apple.

scholarly journals EjBZR1 represses fruit enlargement by binding to the EjCYP90 promoter in loquat

2021 ◽  
Vol 8 (1) ◽  
Author(s):  
Wenbing Su ◽  
Zikun Shao ◽  
Man Wang ◽  
Xiaoqing Gan ◽  
Xianghui Yang ◽  
...  
Keyword(s):  
Large Scale ◽  
Crop Yields ◽  
Fruit Size ◽  
Plant Size ◽  
Cell Number ◽  
Fruit Growth ◽  
Eriobotrya Japonica ◽  
Scale Production ◽  
Virus Induced Gene Silencing ◽  
P450 Gene

AbstractLoquat (Eriobotrya japonica) is a subtropical tree that bears fruit that ripens during late spring. Fruit size is one of the dominant factors inhibiting the large-scale production of this fruit crop. To date, little is known about fruit size regulation. In this study, we first discovered that cell size is more important to fruit size than cell number in loquat and that the expression of the EjBZR1 gene is negatively correlated with cell and fruit size. Virus-induced gene silencing (VIGS) of EjBZR1 led to larger cells and fruits in loquat, while its overexpression reduced cell and plant size in Arabidopsis. Moreover, both the suppression and overexpression of EjBZR1 inhibited the expression of brassinosteroid (BR) biosynthesis genes, especially that of EjCYP90A. Further experiments indicated that EjCYP90A, a cytochrome P450 gene, is a fruit growth activator, while EjBZR1 binds to the BRRE (CGTGTG) motif of the EjCYP90A promoter to repress its expression and fruit cell enlargement. Overall, our results demonstrate a possible pathway by which EjBZR1 directly targets EjCYP90A and thereby affects BR biosynthesis, which influences cell expansion and, consequently, fruit size. These findings help to elucidate the molecular functions of BZR1 in fruit growth and thus highlight a useful genetic improvement that can lead to increased crop yields by repressing gene expression.

scholarly journals Comparison of fruit morphology and nutrition metabolism in different cultivars of kiwifruit across developmental stages

PeerJ ◽  
2021 ◽  
Vol 9 ◽  
pp. e11538
Author(s):  
Yu-fei Li ◽  
Weijia Jiang ◽  
Chunhong Liu ◽  
Yuqi Fu ◽  
Ziyuan Wang ◽  
...  
Keyword(s):  
Fruit Development ◽  
Dry Matter ◽  
Developmental Stages ◽  
Soluble Sugars ◽  
Fruit Size ◽  
Quinic Acid ◽  
Quality Parameters ◽  
Soluble Solids ◽  
Dry Matter Accumulation ◽  
Shape Pattern

Kiwifruit (Actinidia) is becoming increasingly popular worldwide due to its favorable flavour and high vitamin C content. However, quality parameters vary among cultivars. To determine the differences in quality and metabolic parameters of kiwifruit, we monitored the growth processes of ‘Kuilv’ (Actinidia arguta), ‘Hongyang’ (Actinidia chinensis) and ‘Hayward’ (Actinidia deliciosa). We found that ‘Kuilv’ required the shortest time for fruit development, while ‘Hayward’ needed the longest time to mature. The fruit size of ‘Hayward’ was the largest and that of ‘Kuilv’ was the smallest. Furthermore, ‘Hongyang’ showed a double-S shape of dry matter accumulation, whereas ‘Kuilv’ and ‘Hayward’ showed a linear or single-S shape pattern of dry matter accumulation during development. The three cultivars demonstrated the same trend for total soluble solids accumulation, which did not rise rapidly until 90–120 days after anthesis. However, the accumulation of organic acids and soluble sugars varied among the cultivars. During later fruit development, the content of glucose, fructose and quinic acid in ‘Kuilv’ fruit was far lower than that in ‘Hongyang’ and ‘Hayward’. On the contrary, ‘Kuilv’ had the highest sucrose content among the three cultivars. At maturity, the antioxidative enzymatic systems were significantly different among the three kiwifruit cultivars. ‘Hongyang’ showed higher activities of superoxide dismutase than the other cultivars, while the catalase content of ‘Hayward’ was significantly higher than that of ‘Hongyang’ and ‘Kuilv’. These results provided knowledge that could be implemented for the marketing, handling and post-harvest technologies of the different kiwifruit cultivars.

scholarly journals Differences in Cell Number Facilitate Fruit Size Variation in Rabbiteye Blueberry Genotypes

2011 ◽  
Vol 136 (1) ◽  
pp. 10-15 ◽  
Author(s):  
Lisa Klima Johnson ◽  
Anish Malladi ◽  
D. Scott NeSmith
Keyword(s):  
Fruit Development ◽  
Fruit Size ◽  
Size Variation ◽  
Cell Number ◽  
Fruit Weight ◽  
Cell Area ◽  
Vaccinium Ashei ◽  
Cell Production ◽  
University Of Georgia ◽  
Fruit Diameter

Fruit size is a valuable commercial trait in blueberry. The cellular basis of variation in fruit size among rabbiteye blueberry (Vaccinium ashei) genotypes was investigated. Twenty genotypes, including cultivars and advanced selections from the University of Georgia blueberry breeding program, were analyzed. Among the 20 genotypes, fruit weight and fruit diameter varied by over threefold and 1.6-fold, respectively. Regression analysis indicated a linear relationship between fruit weight and fruit diameter (R2 = 0.97, P < 0.001), suggesting that fruit diameter is a good predictor of fruit weight. Among the 20 genotypes, mesocarp cell number and cell area varied by almost 2.5-fold and 1.5-fold, respectively. Although fruit diameter and cell number were significantly related (R2 = 0.79, P < 0.001), no relationship could be established between fruit diameter and cell area. These data indicate that variation in fruit size among rabbiteye blueberry genotypes is primarily facilitated by variation in cell number. Two small and two large fruit size genotypes were further analyzed. Differences in cell number among some of these genotypes were apparent at bloom suggesting that cell production before bloom is an important mechanism contributing to variation in final cell number. Differences in final cell number among other genotypes were manifested during fruit development, indicating that cell production during fruit development was also instrumental in determining variation in final cell number. This study suggests that fruit size variation in rabbiteye blueberry genotypes is determined by mechanisms that regulate cell production before bloom and during fruit development.

scholarly journals Regulation of Fruit Growth and Fruit Size in Apple

HortScience ◽  
2005 ◽  
Vol 40 (4) ◽  
pp. 1097A-1097
Author(s):  
Anish Malladi ◽  
Peter Goldsbrough ◽  
Peter Hirst
Keyword(s):  
Gene Expression ◽  
Cell Cycle ◽  
Cell Division ◽  
Fruit Development ◽  
Fruit Size ◽  
Cell Number ◽  
Rt Pcr ◽  
Cell Production ◽  
Golden Delicious ◽  
Dividing Cells

Fruit development in apple cultivars varying in their ultimate fruit size was analyzed using cytology, flow cytometry (FCM), and semi-quantitative RT-PCR. Fruit size variation across cultivars was largely explained by variation in cell number. The cell division phase lasted for less than 30 days in all varieties, less than previously believed. A distinct overlap between the cell division and cell expansion phases was present. Analysis of the relative cell production rate (rCPR) showed a major peak about 10 days after full bloom (DAFB) after which it declined. Comparison of the rCPR across varieties suggested distinct patterns of cell production with `Gala' having a low but sustained rCPR, `Pixy Crunch' a short but high rCPR, and `Golden Delicious' having a high and sustained rCPR. FCM analysis also showed similar patterns with a peak in the proportion of dividing cells about 10 DAFB followed by a decline. To further understand regulation of cell number, four cell cycle related genes were cloned from `Gala'. Cyclin Dependent Kinase B (CDK B) and Cyclin B were found to be highly cell division phase specific in their expression. Analysis of gene expression by semi-quantitative RT-PCR indicated peak expression of these two genes at 5-10 DAFB, consistent with the peaks in rCPR and proportion of dividing cells. Comparison of gene expression across the varieties showed higher peak expression of the above genes in the larger-fruited `Golden Delicious' than in the smaller-fruited `Gala.' This study provides novel insight into the regulation of fruit development in apple and also suggests a role for the cell cycle genes in fruit size regulation.

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