scholarly journals Mass Rearing and Life Table Attributes of Two Cyclorrhaphan Flies, Lucilia sericata Meigen (Diptera: Calliphoridae) and Musca domestica L. (Diptera: Muscidae) under Laboratory Conditions

2014 ◽  
Vol 11 (5) ◽  
pp. 291-298 ◽  
Author(s):  
Vahid Saleh ◽  
Aboozar Soltani ◽  
Tahere Dabaghmane ◽  
Hamzeh Alipour ◽  
Kourosh Azizi ◽  
...  
2020 ◽  
Vol 113 (3) ◽  
pp. 1211-1220 ◽  
Author(s):  
Yu-Jie Jia ◽  
Bo Wang ◽  
Tong-Xian Liu

Abstract The biocontrol values of natural enemies are strongly correlated to their ability to regulate the density of their host/prey. For parasitoids, apart from parasitism and host feeding, unsuccessful host stinging (i.e., stings that were aborted, abandoned, or discontinued without oviposition or host feeding) can also negatively affect their hosts and host populations. Although several studies have reported unsuccessful host stinging and its impacts on hosts, the effects of this type of attack on host life table parameters are still unclear. In the present study, we used the parasitoid Aphelinus asychis Walker (Hymenoptera: Aphelinidae) and its host Acyrthosiphon pisum (Harris) (Hemiptera: Aphididae) to investigate the influence of unsuccessful host stinging on host populations under laboratory conditions at. Biological parameters of A. pisum were analyzed using an age stage, two-sex life table. The results of this study showed that unsuccessful host stinging was prevalent under laboratory conditions, and the frequency of this type of attack on third- and fourth-instar hosts was higher than the frequencies of parasitism and host feeding. Unsuccessful host stinging adversely impacted aphid populations, by decreasing aphid survival and reproduction, and impacts were greatest in hosts attacked at the first and fourth instars. These results indicate that unsuccessful host stinging enhances the biological control impact of A. asychis attacking A. pisum, and its effect on host populations should also be considered when selecting and mass rearing of parasitoids for biological control.


1999 ◽  
Vol 2 (2) ◽  
pp. 498-502 ◽  
Author(s):  
E.M. El-Kady . ◽  
A.M. Kheirallah . ◽  
A.N. Kayed . ◽  
S.I. Dekinesh . ◽  
Z.A. Ahmed .

1987 ◽  
Vol 65 (5) ◽  
pp. 1158-1166 ◽  
Author(s):  
F. Michael Barrett

A tyrosinase, enzyme A, and a laccase, enzyme B, have been partially purified from larval cuticle of the flesh fly Sarcophaga bullata. Enzyme A (EC 1.10.3.1, o-diphenol: O2 oxidoreductase) oxidizes o-diphenols but not p-diphenols, is strongly inhibited by phenylthiourea, and has a pH optimum around pH 6.5–7.0. Assays on intact cuticle suggest that it becomes maximally activated at pH between 8 and 9. Enzyme B (EC 1.10.3.2, p-diphenol: O2 oxidoreductase) oxidizes both o-diphenols and p-diphenols, is not inhibited by phenylthiourea but is inhibited by concentrations of sodium azide that have little effect on enzyme A, and has a pH optimum near pH 4.5. Enzyme A was identified in extracts of cuticle from nine other species representing five orders. Enzyme B was much less readily extractable but was partially purified from larval cuticle of Phormia regina, Musca domestica, and Lucilia sericata. A summary of all species studied to date makes possible the test of a hypothesis about the distribution of these cuticular phenoloxidases within the Insecta.


1971 ◽  
Vol 125 (2) ◽  
pp. 395-400 ◽  
Author(s):  
P. G. C. Douch ◽  
J. N. Smith

The oxidation of 3,5-di-tert.-butylphenyl N-methylcarbamate (Butacarb) has been studied in the flies Musca domestica and Lucilia sericata, grass grubs Costelytra zealandica and the mouse. In all species eleven oxidation products, which were formed by hydroxylation of the tert.-butyl groups and the N-methyl group, were detected.


2018 ◽  
Vol 11 (7) ◽  
pp. 953-958 ◽  
Author(s):  
Mikhail Alekseevich Levchenko ◽  
Elena Anatol'evna Silivanova ◽  
Ruzilya Khusanovna Bikinyaeva ◽  
Galina Fedorovna Balabanova

2015 ◽  
Vol 114 (9) ◽  
pp. 3525-3528 ◽  
Author(s):  
Q. F. Li ◽  
X. Li ◽  
J. B. Hunag ◽  
D. M. Zhang ◽  
J. Z. Yuan

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