1976
DOI: 10.1016/0305-0491(76)90261-3
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Cuticular lipids of insects—VII Cuticular hydrocarbons of the crickets Achet a domesticus, gryllus pennsylvanicus and Nemobius fasciatus

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Cited by 8 publications
(7 citation statements)
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“…This result is consistent with previous analysis of cuticular hydrocarbons in orthopterans (Soliday et al. , 1974; Nelson & Sukkestad, 1975; Warthen & Uebel, 1980), and is particularly characteristic of crickets (Blomquist et al. , 1976).…”
Section: Discussionsupporting
confidence: 93%
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“…This result is consistent with previous analysis of cuticular hydrocarbons in orthopterans (Soliday et al. , 1974; Nelson & Sukkestad, 1975; Warthen & Uebel, 1980), and is particularly characteristic of crickets (Blomquist et al. , 1976).…”
Section: Discussionsupporting
confidence: 93%
“…Moreover, we found that a high proportion (approximately 80%) of the compounds, are n-alkanes and n-alkenes ranging in chain length from 31 to 33 carbons. This result is consistent with previous analysis of cuticular hydrocarbons in orthopterans (Soliday et al, 1974;Nelson & Sukkestad, 1975;Warthen & Uebel, 1980), and is particularly characteristic of crickets (Blomquist et al, 1976). Using peak retention times in our data analysis, rather than the actual identification of compounds, may have led to the overlooking of hidden variation in chemical profiles.…”
Section: Discussionsupporting
confidence: 89%
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“…In respect to synthesis of 2-methylalkanes either by the parasitized nymph or by the Eretmocerus female, the biosynthetic mechanisms for possible formation of a mono-methyl branched alkane at the 2 position have been established. Various studies on the biosynthesis of 2-methylalkanes in plants (Kolattukudy et al, 1976) and insects Blomquist et al, 1976Blomquist et al, , 1987 suggest that the methyl branch originates from the iso-branched starter piece (isobutyryl-CoA) derived from the branched amino acid, valine. The use of isobutyryl-CoA as the starter for the biosynthetic pathway for the synthesis of alkanes in insects (Nelson, 1993;Nelson and Blomquist, 1995) results in the synthesis of even-carbon numbered alkanes with a methyl branch at the carbon-2 position .…”
Section: Discussionmentioning
confidence: 99%
“…Various studies on the biosynthesis of 2-methylalkanes in plants (Kolattukudy et al, 1976) and insects Blomquist et al, 1976Blomquist et al, , 1987 suggest that the methyl branch originates from the iso-branched starter piece (isobutyryl-CoA) derived from the branched amino acid, valine. The use of isobutyryl-CoA as the starter for the biosynthetic pathway for the synthesis of alkanes in insects (Nelson, 1993;Nelson and Blomquist, 1995) results in the synthesis of even-carbon numbered alkanes with a methyl branch at the carbon-2 position .…”
Section: Discussionmentioning
confidence: 99%