Simultaneous measurement of oxygen and carbon dioxide diffusivity in pear fruit tissue

2003 ◽  
Vol 29 (2) ◽  
pp. 155-166 ◽  
Author(s):  
W Schotsmans ◽  
B.E Verlinden ◽  
J Lammertyn ◽  
B.M Nicolaı̈
2005 ◽  
pp. 243-251
Author(s):  
Q. Tri Ho ◽  
B.E. Verlinden ◽  
P. Verboven ◽  
S. Vandewalle ◽  
B.M. Nicolaï

2007 ◽  
Vol 87 (10) ◽  
pp. 1858-1867 ◽  
Author(s):  
Quang Tri Ho ◽  
Bert E Verlinden ◽  
Pieter Verboven ◽  
Stefan Vandewalle ◽  
Bart M Nicolaï

Plant Disease ◽  
2002 ◽  
Vol 86 (6) ◽  
pp. 625-628 ◽  
Author(s):  
R. A. Spotts ◽  
L. A. Cervantes

d'Anjou pear, the main cultivar grown in the Mid-Columbia Region of Oregon, is subject to russeting of the fruit surface, resulting in reduced quality and value. The role of Aureobasidium pullulans and Rhodotorula glutinis in russet of pear fruit was studied. Inoculations were done at full bloom in 1998 and 1999 and petal fall in 1999 with a log range of concentrations up to 108CFU/ml. Populations of A. pullulans on floral and fruit tissue were monitored during spring 1999 and 2000 in six orchards with a history of russet. Russet of fruit in both studies was evaluated at harvest. In 1998 neither fungus increased russet. In 1999, inoculation with two strains of each fungus at 108 CFU/ml increased russet. Inoculation with 104 or 106 CFU/ml did not increase russet in either year. In commercial orchards, there was no correlation between fruit russet and the populations of A. pullulans on floral and fruit tissue. Populations were less than 103 CFU/g of tissue. We conclude that A. pullulans and R. glutinis are not major contributors to russet of d'Anjou pear fruit in the Mid-Columbia Region.


2005 ◽  
pp. 113-120
Author(s):  
Q. Tri Ho ◽  
B.E. Verlinden ◽  
P. Verboven ◽  
B.M. Nicolaï ◽  
S. Vandewalle

1993 ◽  
Vol 17 (1) ◽  
pp. 77-83 ◽  
Author(s):  
Fang Qian ◽  
Juntao Lu ◽  
Zhongbo Zhou ◽  
Chuansin Cha

HortScience ◽  
1990 ◽  
Vol 25 (11) ◽  
pp. 1355F-1356
Author(s):  
George D. Nanos ◽  
Roger J. Romani ◽  
Adel A. Kader

The response of pear fruits and suspension-cultured pear fruit cells to 0% or 0.25% O2 is being examined to evaluate the feasibility of using such atmospheres for postharvest insect control. These treatments inhibited ethylene production, had no effect on acetaldehyde content, and increased ethanol production in pears kept at 20C for 10 days. The blossom end area of pear fruits was more prone to anaerobiosis, as indicated by increased alcohol dehydrogenase activity and ethanol content. Pear fruit plugs showed increased respiration and ethylene production rates when skin was present compared to plugs without skin. Methods for measuring activity of alcohol dehydrogenase, pyruvate decarboxylase, and pyruvate kinase have been modified and optimized and will be used to determine changes in pear fruit tissue during low O2 treatment and subsequent recovery in air.


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