Nanocarrier‐delivered dsRNA suppresses wing development of green peach aphids

2021 ◽  
Author(s):  
Yun‐Hui Zhang ◽  
Zhong‐Zheng Ma ◽  
Hang Zhou ◽  
Zi‐Jian Chao ◽  
Shuo Yan ◽  
...  
2020 ◽  
Vol 29 (2) ◽  
pp. 195-204
Author(s):  
B.M. Kataev ◽  
M.A. Yeshitla ◽  
J. Schmidt

Omostropus rotundatus Clarke, 1973 from the Bale Mountains (Ethiopia) is transferred to the genus Harpalus Latreille, 1802. Since the name rotundatus was already used in the latter genus, the substitute name Harpalus clarkei Kataev et Schmidt, nom. nov. is proposed for Harpalus rotundatus (Clarke, 1973), comb. nov. (non Dejean, 1829; non Chaudoir, 1844). The diagnostic characters of Harpalus and Omostropus are discussed. Data on distribution and hind wing development of some additional Ethiopian species of Harpalina mostly from the Bale and Arsi Mountains are presented.


2008 ◽  
Vol 98 (9) ◽  
pp. 985-991 ◽  
Author(s):  
R. Srinivasan ◽  
J. M. Alvarez

Hairy nightshade, Solanum sarrachoides, is a solanaceous weed found abundantly in Pacific Northwest potato ecosystems. It serves as a reservoir for one of the important potato viruses, Potato leafroll virus (PLRV) (Luteoviridae: Polerovirus), and its most important vector, the green peach aphid, Myzus persicae (Homoptera: Aphididae). Laboratory research indicated an increased green peach aphid settling and performance on S. sarrachoides than on potato. It also revealed that green peach aphids transmitted PLRV more efficiently from S. sarrachoides to potato than from potato to potato. To test the efficiency of S. sarrachoides as an inoculum source in the field, a two season (2004 and 2005) trial was conducted at Kimberly, Idaho. Two inoculum sources, PLRV-infected potato and PLRV-infected S. sarrachoides, were compared in this trial. Green peach aphid density and temporal and spatial PLRV spread were monitored at weekly intervals. Higher densities of green peach aphids were observed on plots with S. sarrachoides and inoculum sources (PLRV-infected S. sarrachoides and potato) than on plots without S. sarrachoides and inoculum sources. PLRV infection in plots with PLRV-infected S. sarrachoides was similar to or slightly higher than in plots with PLRV-infected potato as an inoculum source. Temporal and spatial PLRV spread was similar in plots with either inoculum source. Thus, S. sarrachoides is as efficient as or a better PLRV inoculum source than potato.


1976 ◽  
Vol 6 (3) ◽  
pp. 425-428 ◽  
Author(s):  
Ehud Arbel ◽  
Tova Arzee

The formation of cork in vertical strips on young branches of Ceratoniasiliqua L. is described. The cork strips represent an early stage in the development of peripheral periderm. Initiation of the cork ridges began with the differentiation of lenticels in vertical rows and further development occurred through the subsequent formation of periderm, primarily in the longitudinal direction. A circumfluent covering of periderm was formed eventually by lateral extension of phellogen leading to the gradual coalescence of the cork strips. Similarities with patterns of cork wing development are discussed.


Nature ◽  
10.1038/39362 ◽  
1997 ◽  
Vol 389 (6651) ◽  
pp. 627-631 ◽  
Author(s):  
Kazuhide Tsuneizumi ◽  
Takuya Nakayama ◽  
Yuko Kamoshida ◽  
Thomas B. Kornberg ◽  
Jan L. Christian ◽  
...  

Development ◽  
1998 ◽  
Vol 125 (15) ◽  
pp. 2951-2962 ◽  
Author(s):  
T. Klein ◽  
A.M. Arias

The Notch signalling pathway plays an important role during the development of the wing primordium, especially of the wing blade and margin. In these processes, the activity of Notch is controlled by the activity of the dorsal specific nuclear protein Apterous, which regulates the expression of the Notch ligand, Serrate, and the Fringe signalling molecule. The other Notch ligand, Delta, also plays a role in the development and patterning of the wing. It has been proposed that Fringe modulates the ability of Serrate and Delta to signal through Notch and thereby restricts Notch signalling to the dorsoventral boundary of the developing wing blade. Here we report the results of experiments aimed at establishing the relationships between Fringe, Serrate and Delta during wing development. We find that Serrate is not required for the initiation of wing development but rather for the expansion and early patterning of the wing primordium. We provide evidence that, at the onset of wing development, Delta is under the control of apterous and might be the Notch ligand in this process. In addition, we find that Fringe function requires Su(H). Our results suggest that Notch signalling during wing development relies on careful balances between positive and dominant negative interactions between Notch ligands, some of which are mediated by Fringe.


Development ◽  
2002 ◽  
Vol 129 (16) ◽  
pp. 3815-3823 ◽  
Author(s):  
Florencia Cavodeassi ◽  
Isabel Rodríguez ◽  
Juan Modolell

During development, the imaginal wing disc of Drosophila is subdivided along the proximal-distal axis into different territories that will give rise to body wall (notum and mesothoracic pleura) and appendage (wing hinge and wing blade). Expression of the Iroquois complex (Iro-C) homeobox genes in the most proximal part of the disc defines the notum, since Iro-C– cells within this territory acquire the identity of the adjacent distal region, the wing hinge. Here we analyze how the expression of Iro-C is confined to the notum territory. Neither Wingless signalling, which is essential for wing development, nor Vein-dependent EGFR signalling, which is needed to activate Iro-C, appear to delimit Iro-C expression. We show that a main effector of this confinement is the TGFβ homolog Decapentaplegic (Dpp), a molecule known to pattern the disc along its anterior-posterior axis. At early second larval instar, the Dpp signalling pathway functions only in the wing and hinge territories, represses Iro-C and confines its expression to the notum territory. Later, Dpp becomes expressed in the most proximal part of the notum and turns off Iro-C in this region. This downregulation is associated with the subdivision of the notum into medial and lateral regions.


1967 ◽  
Vol 60 (5) ◽  
pp. 1088-1091 ◽  
Author(s):  
R. C. Dickson ◽  
E. F. Laird
Keyword(s):  

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