Agrobacterium-mediated transformation of black cherry for flowering control and insect resistance

2014 ◽  
Vol 119 (1) ◽  
pp. 107-116 ◽  
Author(s):  
Ying Wang ◽  
Paula M. Pijut
2018 ◽  
Author(s):  
Christine Kronfoth ◽  
◽  
Peter Grayson ◽  

HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 526d-526
Author(s):  
M. Freeman ◽  
C. Walters ◽  
M.A. Thorpe ◽  
T. Gradziel

Almond, as with other stone fruit, possesses a highly lignified endocarp or shell. The dominant hard-shelled trait (D-) is positively associated with greater resistant to insect infestation than nuts expressing the paper-shelled (dd) trait. Hard-shelled genotypes have undesirable effects, including a lower kernel meat-to-nut crack-out ratio, greater kernel damage during mechanical shelling, and a reduction in plant energy available to kernel development. Histogenic analysis shows that the almond endocarp, unlike peach, has a tri-partite structure. Insect feeding studies have subsequently demonstrated that the inner endocarp layer, which is similar in both hard and paper-shelled types, is the most important structural barrier to insect infestation. Shell-seal integrity and X-ray studies have confirmed that discontinuities at the inner endocarp suture seal are the primary, though not the sole site of entry for insect pests. Paper-shelled almond selections with highly lignified and well-sealed inner endocarps show resistance levels comparable to hard shelled types but with crack-out ratios 30% to 40% higher. Pseudo-paper-shelled types have also been selected, in which a highly lignified outer endocarp is formed, but is retained by the fruit hull at dehiscence. An understanding of endocarp morphology and development is thus important in breeding for insect resistance as well as the commercial utilization of both kernel and hull.


1992 ◽  
Vol 57 ◽  
Author(s):  
D. Maddelein ◽  
N. Lust

The  study of a seventy years old stand of Scots pine on drift sands proves that  Scots pine growth on these sites was and is still relatively good: average  diameter 27.6 cm, average height 19.4 m, standing volume 213 m3 and an annual increment  of 4.9 m3.ha-1.yr-1. All Scots pines  belong to the upper storey. Yet considerable differences in crown development  and vitality are observed. The current growth rate and the spontaneous  settlement of pine seedlings under canopy show the ideal conditions for the  creation of a high forest with reserves. Anyway a rotation period of more  than 70 years is recommendable.     On several places a consolidated regeneration of Scots pine seedlings under  canopy occur. Groups with a stem number of 700 to 3,500 seedlings per are, ranging  in age from 3 to 11 years and in height from 10 to 170 cm, are present. This  Scots pine regeneration has developed in a normal mor humus layer and in a  dense Deschampsia mat.      Broadleaved regeneration is not so abundant, and consists for 75 % of black  cherry. Absence of seed trees, browsing damage and the exclusive character of  black cherry are the limiting factors for the installation and survival of  valuable indigenous species, such as pedunculate oak.     Provided that black cherry is removed and that the regeneration is  protected against wild damage, it is possible to create a mixed forest  dominated by Scots pine but with a considerable admixture of indigenous  broadleaved trees. However, if black cherry will not be sufficiently  controlled, it can be expected that in a first phase black cherry will  dominate the understorey, that it will prevent the regeneration of all other  species and that, very soon, it will form an almost single-species dominated  stage in forest succession.


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