Barbarea vulgaris: Lansdown, R.V.

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2004 ◽  
Vol 94 (6) ◽  
pp. 509-516 ◽  
Author(s):  
Jian-hua Lu ◽  
Shu-sheng Liu ◽  
A.M. Shelton

AbstractThe term ‘dead-end trap cropping’ has recently been proposed to identify a plant that is highly attractive for oviposition by an insect pest, but on which offspring of the pest cannot survive. The potential of the wild crucifer Barbarea vulgaris R. Br. to allure and serve as a dead-end trap crop for the diamondback moth Plutella xylostella (L.), an important pest of cruciferous crops worldwide, was examined in laboratory experiments. When P. xylostella adults were provided with a dual-choice of plants of B. vulgaris, and Chinese cabbage Brassica campestris (L.), in one arena, adult moths laid 2.5–6.8 times more eggs on the former than on the latter. When P. xylostella adults were provided with a dual-choice of plants of B. vulgaris and common cabbage Brassica oleracea L., adult moths laid virtually all their eggs on the former and ignored the latter. Nearly all P. xylostella eggs laid on the three species of plants hatched successfully, but nearly all individuals on plants of B. vulgaris died as neonates or early instar larvae, while 87–100% of the larvae on Chinese cabbage and common cabbage survived to pupation. Dual choice tests with a Y-tube olfactometer showed that volatiles from B. vulgaris were much more attractive to P. xylostella adults than those from common cabbage. The results demonstrate that B. vulgaris has a great potential as a dead-end trap crop for improving management of P. xylostella. Factors that may influence the feasibility of using B. vulgaris as a trap crop in the field are discussed, and ways to utilize this plant are proposed.


2009 ◽  
Vol 151 (4) ◽  
pp. 1977-1990 ◽  
Author(s):  
Vera Kuzina ◽  
Claus Thorn Ekstrøm ◽  
Sven Bode Andersen ◽  
Jens Kvist Nielsen ◽  
Carl Erik Olsen ◽  
...  

2012 ◽  
Vol 30 (4) ◽  
pp. 506-512 ◽  
Author(s):  
Fiorello Toneatto ◽  
Thure P. Hauser ◽  
Jens Kvist Nielsen ◽  
Marian Ørgaard

1955 ◽  
Vol 47 (2) ◽  
pp. 104-105
Author(s):  
Marvin M. Schreiber ◽  
Stanford N. Fertig

1974 ◽  
Vol 52 (10) ◽  
pp. 916-921 ◽  
Author(s):  
D. Dörnemann ◽  
W. Löffelhardt ◽  
H. Kindl

A chemical synthesis of specifically 14C-labelled 2-benzylmalic acid, hitherto unknown, was developed. 4-Phenylacetoacetate obtained by condensation of phenylacetyl chloride-1-14C with ethyl acetoacetate yielded 2-benzylmalic acid-2-14C after cyanohydrin reaction and hydrolysis.2-Benzylmalic acid-2-14C, administered to shoots of Nasturtium officinale and Barbarea vulgaris, was shown to be an efficient precursor of the aglucone moiety of the mustard oil glucoside gluconasturtiin. The incorporation of radioactivity agreed well with the values reported for incorporation of 3-benzylmalic acid, but was considerably higher than that obtained after application of L-phenylalanine-U-14C. A conversion of 2-benzylmalic acid into 3-benzylmalic acid and 2-amino-4-phenylbutyric acid could also be demonstrated. These findings provide the final evidence for a chain-lengthening mechanism leading to homologous amino acids as proposed by Underbill and Wetter in 1966.


2006 ◽  
Vol 67 (12) ◽  
pp. 1214-1223 ◽  
Author(s):  
Hanneke van Leur ◽  
Ciska E. Raaijmakers ◽  
Nicole M. van Dam

2011 ◽  
Vol 59 (13) ◽  
pp. 6947-6956 ◽  
Author(s):  
Lea Dalby-Brown ◽  
Carl Erik Olsen ◽  
Jens Kvist Nielsen ◽  
Niels Agerbirk
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