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PREDATORY MITES IN IPM<br />
321<br />
effect was additive, multiplicative or detrimental in the action of predators. The notoverlapping<br />
degree of specialization, narrow in P. persimilis, wider in N.<br />
californicus, <strong>and</strong> the consequent asymmetry in the response guaranteed, for some<br />
weeks, fast (mainly due to P. persimilis) <strong>and</strong> longer (mainly due to N. californicus)<br />
term equilibrium of the prey-predator system <strong>and</strong> of biological control, especially on<br />
eggplant <strong>and</strong> pepper.<br />
As concerns the ascertained intrinsic traits <strong>and</strong> versatility of some phytoseiid, N.<br />
californicus appears able to adapt to different food <strong>and</strong> climatic conditions<br />
(Castagnoli & Simoni, 2004), <strong>and</strong> it may be considered feasible <strong>and</strong> convenient if<br />
combined to or in light shifts of phytoseiid releases, or in application with some<br />
other kind of biocontrol agents (i.e. other mites, insects or the fungus Beauveria<br />
bassiana). Obviously, the adoption of such a tactic needs an intensive monitoring, a<br />
full evaluation of the possible effect of the micr<strong>org</strong>anism on the predator <strong>and</strong> an<br />
assessment concerning the possibility that the phytoseiid is able to recognize the<br />
treated substrate (Simoni, Guidi, & Tarchi, 2009).<br />
3.5. Cannibalism <strong>and</strong> Intraguild Predation<br />
The coexistence <strong>and</strong> interaction of two different phytoseiids species sharing a<br />
common prey resource can undoubtedly determine new functional-trophic relations<br />
(Rudolf, 2008). Intraguild predation <strong>and</strong> cannibalism are, in cases of combined<br />
release of predators, variables to be included in current models aiming at<br />
overcoming the discrepancy between theory <strong>and</strong> empirical data.<br />
Although cannibalism may often represent a weak, unuseful interaction in<br />
nature, it may have significant consequences at the population level (McCann,<br />
Hastings, & Huxel, 1998). Cannibalism can be a crucial factor contributing to<br />
population structure, dynamics <strong>and</strong> control in a given habitat (McCann et al., 1998),<br />
affecting the quantity <strong>and</strong> quality of food for the remaining individuals. Predatorpredator<br />
interactions such as competition, intraguild predation (IGP), <strong>and</strong><br />
cannibalism affect the development <strong>and</strong> coexistence of predator populations, <strong>and</strong><br />
can have significance in the biological control of commonly exploited pest<br />
<strong>org</strong>anisms (Castagnoli, Liguori, & Simoni, 2002; Schausberger & Croft, 2000).<br />
Furthermore, phytoseiids are suitable models for studying cannibalism <strong>and</strong> related<br />
phenomena, due to their diversity <strong>and</strong> variability, small size <strong>and</strong> ease of rearing in<br />
the laboratory. In future research <strong>and</strong> in the frame of tactics <strong>and</strong> strategies of control,<br />
most fields are to be exploited, i.e. kin the link of cannibalism with discrimination<br />
<strong>and</strong> disease transmission, the interplay between cannibalism <strong>and</strong> dispersal, <strong>and</strong> the<br />
effects of cannibalism on population dynamics <strong>and</strong> species communities.<br />
4. CONCLUSIONS<br />
Given the number <strong>and</strong> complexity of factors involved in the wide pattern of natural<br />
enemies <strong>and</strong> antagonists, phytoseiid mites appear able to significantly interact in the<br />
dynamic equilibria of different prey-crop contexts. The modality of agricultural<br />
pests control <strong>by</strong> these predators can range from classical biological control, with<br />
introduction <strong>and</strong> establishment of foreign species, to safeguard <strong>and</strong> augmentation of