Functional Response, Prey Stage Preference, and Mutual Interference of the Tamarixia triozae (Hymenoptera: Eulophidae) on Tomato and Bell Pepper

2015 ◽  
Vol 108 (2) ◽  
pp. 414-424 ◽  
Author(s):  
X.-B. Yang ◽  
M. Campos-Figueroa ◽  
A. Silva ◽  
D. C. Henne
2009 ◽  
Vol 2009 ◽  
pp. 1-9 ◽  
Author(s):  
Lijuan Chen ◽  
Liujuan Chen

This paper discusses a discrete periodic Volterra model with mutual interference and Holling II type functional response. Firstly, sufficient conditions are obtained for the permanence of the system. After that, we give an example to show the feasibility of our main results.


2010 ◽  
Vol 2010 ◽  
pp. 1-11 ◽  
Author(s):  
Runxin Wu

This paper discuss a discrete periodic Volterra model with mutual interference and Beddington-DeAngelis functional response. By using the comparison theorem of difference equation, sufficient conditions are obtained for the permanence of the system. After that,we give an example to show the feasibility of our main result.


2020 ◽  
Vol 25 (6) ◽  
pp. 1147-1157
Author(s):  
Rosenya Michely Cintra Filgueiras ◽  
Jairo De Almeida Mendes ◽  
Francisco Wesller Batista Da Silva ◽  
Eduardo Pereira De Sousa Neto ◽  
José Wagner Da Silva Melo

Raoiella indica Hirst (Acari: Tenuipalpidae) is a polyphagous pest widely dispersed worldwide and a particular threat to crops from the Arecaceae family. Control measures are still being evaluated in recently invaded countries. A possible control strategy for this pest is the use of predatory mites. A recent study has suggested Neoseiulus barkeri Hughes (Acari: Phytoseiidae) as a potential biological control agent of R. indica. In the present study we determined the prey stage preference of N. barkeri when offered different stages of R. indica besides its functional response and numerical over its prey stage preferred. The predatory mite N. barkeri showed a marked preference for eggs over other stages of the prey. The regression analysis indicated that the predatory mite N. barkeri exhibited a Type II functional response. The prey density needed to start the oviposition was 10 R. indica eggs. The number of eggs laid by N. barkeri females increased with an increase in the prey density and tended to stabilize when prey availability was greater than 80 R. indica eggs, with average oviposition of 2 eggs/female. Our study suggests that N. barkeri shows potential to reduce populations of R. indica, especially at low prey densities. However, further studies are needed to investigate whether R. indica supports the development of immature stages of N. barkeri.


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