The tamarillo: Fruit growth and maturation, ripening, respiration, and the role of ethylene

1976 ◽  
Vol 27 (5) ◽  
pp. 399-404 ◽  
Author(s):  
Harlan K. Pratt ◽  
Michael S. Reid
Keyword(s):  
HortScience ◽  
1994 ◽  
Vol 29 (5) ◽  
pp. 440a-440
Author(s):  
Rémy E Milad ◽  
Kenneth A Shackel

End cracking of French prune fruits occurs when previously water stressed trees are irrigated during early July. Fruit phloem, xylem and transpiration flows (P, X and T, respectively) were measured diurnally during 72 h periods in mid June, early July and mid July (before, during and after the crack-susceptible period). Midway through each 72 h period, the previously stressed trees were irrigated. In mid June, X was larger than P, whereas P was larger than X during early July. In mid July, P and X were similar. In early July, the period preceding irrigation was characterized by an ourflow of phloem sap during the day and phloem inflow during the night. After irrigation, larger phloem inflows were observed and no phloem outflow occurred. Fruit transpiration rates were highly correlated with VPD. They exhibited a gradual decrease during the season, reaching minimum values during early July, before increasing again. The sum of P and X was virtually identical for the three periods i.e. stronger P's compensated for weaker X's and vice versa. Our results suggest that properties intrinsic to the fruit play the primary role in modulating water and photosynthate movements between the tree and the fruit. The possible role of these properties on fruit growth and cracking will be examined.


2005 ◽  
Vol 124 (3) ◽  
pp. 371-380 ◽  
Author(s):  
Saneyuki Kawabata ◽  
Haruka Sasaki ◽  
Ryozo Sakiyama

2000 ◽  
Vol 75 (4) ◽  
pp. 413-422 ◽  
Author(s):  
C. J. Stanley ◽  
D. S. Tustin ◽  
G. B. Lupton ◽  
S. Mcartney ◽  
W. M. Cashmore ◽  
...  

1996 ◽  
Vol 121 (4) ◽  
pp. 676-679 ◽  
Author(s):  
K. Yonemori ◽  
A. Itai ◽  
R. Nakano ◽  
A. Sugiura

The role of calyx lobes in CO2 exchange in persimmon (Diospyros kaki Thunb.) fruit was investigated during fruit growth and development. Carbon dioxide exchange rates of attached and detached fruit were measured in light and dark conditions in the field after calyx lobes were removed. Calyx lobes were removed at fruit growth stages I and III, which were defined as the period when fruit diameter increases >0.3 mm·d-1 (Zheng et al., 1990). Removing calyx lobes at stage I significantly inhibited fruit growth, while removing them at stage III had no effect on growth. Two weeks after calyx lobes were removed at stage I, CO2 exchange decreased 80% in light and dark conditions compared with the control fruit. The rapid decreases of CO2 exchange rate by calyx lobe removal at stage I were obvious if expressed per fruit or on a fresh weight basis. In contrast, treatment at stage III had no effect on CO2 exchange rate of fruit and no effect on fruit growth. However, when the calyx lobe scars were sealed with Vaseline soon after calyx lobe removal at stage III, an immediate decline in CO2 exchange rate in the dark occurred with simultaneous inhibition of the final swell in fruit growth. A possible relationship between fruit growth potential and gas-exchange capacity is discussed.


2010 ◽  
Vol 62 (5) ◽  
pp. 727-741 ◽  
Author(s):  
Elodie Mathieu-Rivet ◽  
Frédéric Gévaudant ◽  
Adrien Sicard ◽  
Sophie Salar ◽  
Phuc Thi Do ◽  
...  

Planta ◽  
1997 ◽  
Vol 201 (4) ◽  
pp. 446-455 ◽  
Author(s):  
Maria J. Rodrigo ◽  
José L. García-Martínez ◽  
Cristina M. Santes ◽  
Paul Gaskin ◽  
Peter Hedden

1968 ◽  
Vol 21 (6) ◽  
pp. 1103 ◽  
Author(s):  
D I Jackson

Gibberellic acid and a mixture of gibberellin A4 and gibberellin A7 each induced seedless fruit development in plum. Parthenocarpic fruits grew more rapidly early in the season but their final diameters were only 60% of control. Hormones applied only to developing vegetative shoots and not to neighbouring flowers did not induce parthenocarpy. The role of hormones in fruit growth is discussed.


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