Mechanisms of Olfaction in Insects - ResearchSpace@Auckland ...
Mechanisms of Olfaction in Insects - ResearchSpace@Auckland ...
Mechanisms of Olfaction in Insects - ResearchSpace@Auckland ...
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General Introduction 3<br />
moth <strong>in</strong> locat<strong>in</strong>g the „call<strong>in</strong>g‟ female over long distances. Lepidopteran sex<br />
pheromones are mostly composed <strong>of</strong> blends <strong>of</strong> two or more compounds (major and<br />
m<strong>in</strong>or pheromone components) <strong>in</strong> specific ratios (Butenandt et al., 1961; Arn et al.,<br />
1986). The ratios are species-specific and the pheromone may fail to elicit a response<br />
<strong>in</strong> males if altered. Sex pheromones are ma<strong>in</strong>ly composed <strong>of</strong> C10 to C18 unsaturated,<br />
straight cha<strong>in</strong> hydrocarbons together with an oxygenated functional group, for<br />
<strong>in</strong>stance an alcohol, acetate ester or aldehyde (Arn et al., 1992; Jurenka, 2003). Sex<br />
pheromone components <strong>in</strong> Lepidoptera are synthesised from fatty acids via enzymes<br />
such as acetyl-CoA, followed by desaturation whereby double bonds are placed at<br />
specific positions along the carbon cha<strong>in</strong>. Limited cha<strong>in</strong> shorten<strong>in</strong>g reactions then<br />
shorten the carbon cha<strong>in</strong> to the appropriate length and f<strong>in</strong>ally reductive modification<br />
<strong>of</strong> the carbonyl carbon generates the functional group (Foster and Roel<strong>of</strong>s, 1987;<br />
Foster and Dugdale, 1988; Jurenka, 2003).<br />
1.3.2 Other odorants detected by moths<br />
The extreme sensitivity and specificity <strong>of</strong> sex pheromone reception has made it the<br />
ideal model for study <strong>of</strong> olfaction <strong>in</strong> moths. However, other odorants such as plant<br />
volatiles <strong>in</strong>clud<strong>in</strong>g esters, aldehydes, alcohols, terpenes and carbon dioxide are also<br />
detected by the moth‟s olfactory system (Kaissl<strong>in</strong>g, 1971). These odorants are used by<br />
moths to locate host plants, oviposition sites and food sources. For example, l<strong>in</strong>alool,<br />
a plant volatile, is suggested to be used by B. mori, Heliothis virescens, Helicoverpa<br />
armigera and Spodoptera littoralis <strong>in</strong> host plant location for lay<strong>in</strong>g eggs (He<strong>in</strong>bockel<br />
and Kaissl<strong>in</strong>g, 1996; Angioy et al., 2003; Røstelien et al., 2005; Anderson et al.,<br />
2009). Herbivore-<strong>in</strong>duced volatiles, which are released by plants <strong>in</strong> response to <strong>in</strong>sect<br />
feed<strong>in</strong>g, result <strong>in</strong> the recruitment <strong>of</strong> beneficial <strong>in</strong>sects that parasitise the <strong>in</strong>fest<strong>in</strong>g<br />
<strong>in</strong>sects. One such example is methyl salicylate, which is detected by moths such as<br />
Mamestra brassica, S. littoralis, and Epiphyas postvittana as a warn<strong>in</strong>g that a plant is<br />
already occupied and thus females avoid such plants for lay<strong>in</strong>g eggs (Suckl<strong>in</strong>g et al.,<br />
1996; Jönsson and Anderson, 1999; Ulland et al., 2008). This is a survival mechanism<br />
used by the moths <strong>in</strong> order to m<strong>in</strong>imise competition once the larvae hatch. Eugenol,<br />
geraniol and citral have also been shown to act as oviposition deterrents for E.<br />
postvittana, while hexanal, l<strong>in</strong>alool, nonanol, octanol and nonanal act as attractants.<br />
Plant volatiles such as citral, nonanol, octanol and n-decylaldehyde have been shown