01.02.2013 Views

Insect Control: Biological and Synthetic Agents - Index of

Insect Control: Biological and Synthetic Agents - Index of

Insect Control: Biological and Synthetic Agents - Index of

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

418 11: Entomopathogenic Fungi <strong>and</strong> their Role in Regulation <strong>of</strong> <strong>Insect</strong> Populations<br />

Another example <strong>of</strong> an establishment in a<br />

completely new environment was the release <strong>of</strong> an<br />

Israeli isolate <strong>of</strong> Z. radicans to control the clover<br />

aphid Therioaphis trifolii in Australia. The experiments<br />

were limited in time <strong>and</strong> the area studied was<br />

small, yet it was shown that dispersal <strong>of</strong> the fungus<br />

up to at least 65 m took place within 2 months <strong>of</strong><br />

release (Milner et al., 1982). Another isolate <strong>of</strong> this<br />

same species was released in Illinois in 1984 to<br />

control the potato leafhopper, Empoasca fabae<br />

(McGuire et al., 1987a). Epizootics <strong>of</strong> Z. radicans<br />

then occurred in E. fabae <strong>and</strong> contributed to regulation<br />

<strong>of</strong> the population, <strong>and</strong> there was evidence to<br />

suggest that one <strong>of</strong> the isolates might have become<br />

established (McGuire et al., 1987b).<br />

Neozygites floridana from South America has<br />

been considered for classical biological control<br />

<strong>of</strong> the cassava green mite (Mononychellus tanajore)<br />

in Africa (Elliot et al., 2000). The data on dispersal<br />

in plots in Brazil indicated that the fungus would<br />

be capable <strong>of</strong> spread under African conditions<br />

<strong>and</strong> contribute to long-term control <strong>of</strong> the pest.<br />

However, it was concluded that N. floridana<br />

would not be capable <strong>of</strong> providing adequate<br />

control <strong>of</strong> the mite if used as the sole control<br />

agent. Releases <strong>of</strong> the Brazilian isolate were<br />

made in Benin in 1999 (Hountondji et al., 2002).<br />

Postrelease monitoring revealed that the introduced<br />

isolate had become established, with infection<br />

prevalences <strong>of</strong> up to 36%, 48 weeks after initial<br />

introduction.<br />

The use <strong>of</strong> fungi for classical biological control is<br />

at the present time a rather difficult issue. First, one<br />

must find a potential agent that does not already<br />

occur in the chosen environment. Then, laboratory<br />

studies are warranted to document that the proposed<br />

agent has potential for classical biological<br />

control. Finally, the authorities must be convinced<br />

that the agent for release <strong>and</strong> establishment poses no<br />

harm to the native fauna, <strong>and</strong> this is difficult, but<br />

not impossible, to accomplish (Hajek <strong>and</strong> Goettel,<br />

2000; Goettel <strong>and</strong> Hajek, 2001). Today, the latter<br />

is difficult to achieve, due to the present attitude<br />

in society that more or less dem<strong>and</strong>s zero risk to<br />

biodiversity.<br />

11.9. Role in Conservation Biocontrol<br />

Conservation biological control (sometimes also<br />

called habitat manipulation) is defined as<br />

Modification <strong>of</strong> the environment or existing practices<br />

to protect <strong>and</strong> enhance specific natural enemies or<br />

other organisms to reduce the effect <strong>of</strong> pests<br />

Eilenberg et al. (2001)<br />

It is probably the most attractive among all strategies<br />

for biological control, yet the least studied.<br />

No agents are released, but the farming systems <strong>and</strong><br />

practice are modified in order to stimulate the naturally<br />

occurring predators, parasitoids, <strong>and</strong> insect<br />

pathogens, to regulate the pest insect populations<br />

below the damage threshold (Barbosa, 1998). Sufficient<br />

regulation by entomophthoralean fungi <strong>and</strong><br />

other natural enemies may actually already exist<br />

for the vast number <strong>of</strong> crop herbivorous insect <strong>and</strong><br />

mite species, which never do any damage because <strong>of</strong><br />

low densities. The conservation strategy also fits<br />

well into modern sustainable agriculture, where<br />

actions to make direct use <strong>of</strong> the naturally occurring<br />

enemies <strong>of</strong> pests are taken into consideration,<br />

including increasing biodiversity <strong>and</strong> supporting a<br />

positive interaction between the crop, the flora,<br />

<strong>and</strong> fauna within the field <strong>and</strong> field margins, <strong>and</strong><br />

l<strong>and</strong>scape elements (Gurr <strong>and</strong> Wratten, 2000;<br />

L<strong>and</strong>is et al., 2000). Fungi from the order Entomophthorales<br />

fit very well into this strategy (Pell<br />

et al., 2001). They have the ability to establish natural<br />

epizootics depending on the host insect <strong>and</strong> a<br />

number <strong>of</strong> biotic <strong>and</strong> abiotic factors. A number <strong>of</strong><br />

entomophthoralean species exist in each field, forest,<br />

private garden, greenhouse, stable <strong>and</strong> nature<br />

area. Certainly, this diversity <strong>of</strong> species (<strong>and</strong> isolates<br />

from each species) could be explored <strong>and</strong> exploited<br />

in conservation biological control.<br />

Each system should be analyzed adequately.<br />

Studies on the epizootiology <strong>of</strong> N. fresenii in the<br />

cotton aphid, Aphis gossypii, in Arkansas have<br />

demonstrated that it is possible to monitor <strong>and</strong><br />

to some extent predict the epizootic development<br />

<strong>of</strong> the fungus in the target insect population<br />

(Hollingsworth et al., 1995; Steinkraus et al.,<br />

1996; Pell et al., 2001). The monitoring <strong>of</strong> the<br />

pest insect can therefore be supplemented with<br />

knowledge on the symptoms <strong>of</strong> fungal disease in<br />

the host, which would allow extension <strong>of</strong>ficers to<br />

modify their recommendations <strong>of</strong> intervention;<br />

e.g., if the pest population is high, but fungus<br />

infected, no pesticide treatment would be required<br />

as the pest population would soon succumb to the<br />

disease.<br />

Habitat manipulation <strong>and</strong> modification <strong>of</strong> existing<br />

practices are <strong>of</strong>ten proposed as means to promote<br />

infections caused by entomopathogenic fungi (Pell<br />

et al., 2001): more hedges, less spraying with<br />

chemicals (e.g., fungicides), <strong>and</strong> irrigation are all,<br />

at least theoretically, supportive to development <strong>of</strong><br />

natural fungal epizootics among pest insects. It was

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!