Plant Silicon Amendment Does Not Reduce Population Growth of Schizaphis graminum or Host Quality for the Parasitoid Lysiphlebus testaceipes

2020 ◽  
Vol 49 (5) ◽  
pp. 745-757
Author(s):  
M V Sampaio ◽  
G M Franco ◽  
D T Lima ◽  
A R C Oliveira ◽  
P F Silva ◽  
...  
2009 ◽  
Vol 76 (2) ◽  
pp. 251-257
Author(s):  
R.S. Cavalcanti ◽  
A. Moino Junior ◽  
E.S. Loureiro ◽  
L.A. Mendonça ◽  
A. Arnosti

RESUMO As interações entre patógenos e parasitóides devem ser avaliadas para um possível controle das pragas, sendo observada a interrupção ou não do desenvolvimento larval quando um hospedeiro parasitado é infectado ou quando um hospedeiro infectado é oferecido ao parasitóide. O objetivo deste trabalho foi avaliar o melhor tempo de liberação do parasitóide Lysiphlebus testaceipes e a melhor concentração dos fungos Beauveriabassiana, Metarhizium anisopliae, Paecilomyces fumosoroseus e Lecanicillium lecanii no controle do pulgão Schizaphis graminum. Os parasitóides foram liberados às 0, 24, 48 e 72 horas após aplicação de duas concentrações (104 e 108 conídios/mL) dos fungos B. bassiana, M. anisopliae, P. fumosoroseus e L. lecanii. Na testemunha foi pulverizada água destilada esterilizada. O fungo entomopatogênico L. lecanii é altamente prejudicial ao desenvolvimento do parasitóide na maior concentração. Para a utilização conjunta dos fungos B. bassiana, M. anisopliae e P. fumosoroseus com L. testaceipes no controle de S. graminum, a melhor época de liberação do parasitóide é logo após a sua aplicação (0h).


1988 ◽  
Vol 120 (12) ◽  
pp. 1079-1083 ◽  
Author(s):  
T.J. Kring ◽  
J.B. Kring

AbstractThe fecundity and reproductive longevity of Schizaphis graminum (Rondani) parasitized by Lysiphlebus testaceipes (Cresson) were determined in the laboratory under four temperature regimes. Daily reproduction by S. graminum declined rapidly after parasitization except at a relatively low temperature regime (12–16 °C). The mean progeny production by parasitized aphids of 2.75 ± 0.08 nymphs per parasitized adult was not significantly different than that for unparasitized aphids (2.94 ± 0.23 nymphs) during the period of time equal to the reproductive life of parasitized aphids. Reproductive longevity of parasitized aphids was longest at the lowest temperature (5.67 ± 0.25 days at 12–16 °C). No significant differences were observed in total progeny produced at different temperatures. The number of progeny within parasitized nulliparous adults (3.37 ± 0.33) as determined by dissections was not significantly different from the mean total progeny produced by parasitized aphids. Parasitization thus seems to interfere with oogenesis, but not with embryonic development or progeny deposition.


2001 ◽  
Vol 67 (9) ◽  
pp. 4233-4241 ◽  
Author(s):  
Stephen T. Abedon ◽  
Troy D. Herschler ◽  
David Stopar

ABSTRACT Bacteriophages (phages) modify microbial communities by lysing hosts, transferring genetic material, and effecting lysogenic conversion. To understand how natural communities are affected it is important to develop predictive models. Here we consider how variation between models—in eclipse period, latent period, adsorption constant, burst size, the handling of differences in host quantity and host quality, and in modeling strategy—can affect predictions. First we compare two published models of phage growth, which differ primarily in terms of how they model the kinetics of phage adsorption; one is a computer simulation and the other is an explicit calculation. At higher host quantities (∼108 cells/ml), both models closely predict experimentally determined phage population growth rates. At lower host quantities (107 cells/ml), the computer simulation continues to closely predict phage growth rates, but the explicit model does not. Next we concentrate on predictions of latent-period optima. A latent-period optimum is the latent period that maximizes the population growth of a specific phage growing in the presence of a specific quantity and quality of host cells. Both models predict similar latent-period optima at higher host densities (e.g., 17 min at 108 cells/ml). At lower host densities, however, the computer simulation predicts latent-period optima that are much shorter than those suggested by explicit calculations (e.g., 90 versus 1,250 min at 105 cells/ml). Finally, we consider the impact of host quality on phage latent-period evolution. By taking care to differentiate latent-period phenotypic plasticity from latent-period evolution, we argue that the impact of host quality on phage latent-period evolution may be relatively small.


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