scholarly journals Pharmacophagy in green lacewings (Neuroptera: Chrysopidae:Chrysopaspp.)?

PeerJ ◽  
2016 ◽  
Vol 4 ◽  
pp. e1564 ◽  
Author(s):  
Jeffrey R. Aldrich ◽  
Kamal Chauhan ◽  
Qing-He Zhang

Green lacewings (Neuroptera: Chrysopidae) are voracious predators of aphids and other small, soft-bodied insects and mites. Earlier, we identified (1R,2S,5R,8R)-iridodial from wild males of the goldeneyed lacewing,Chrysopa oculataSay, which is released from thousands of microscopic dermal glands on the abdominal sterna. Iridodial-baited traps attractC. oculataand otherChrysopaspp. males into traps, while females come to the vicinity of, but do not usually enter traps. Despite their healthy appearance and normal fertility, laboratory-rearedC. oculatamales do not produce iridodial. Surprisingly, goldeneyed lacewing males caught alive in iridodial-baited traps attempt to eat the lure and, in Asia, males of otherChrysopaspecies reportedly eat the native plant,Actinidia polygama(Siebold & Zucc.) Maxim. (Actinidiaceae) to obtain the monoterpenoid, neomatatabiol. These observations suggest thatChrysopamales must sequester exogenous natural iridoids in order to produce iridodial; we investigated this phenomenon in laboratory feeding studies. Lacewing adult males fed various monoterpenes reduced carbonyls to alcohols and saturated double bonds, but did not convert these compounds to iridodial. Only males fed the common aphid sex pheromone component, (1R,4aS,7S,7aR)-nepetalactol, produced (1R,2S,5R,8R)-iridodial. Furthermore, althoughC. oculatamales fed the second common aphid sex pheromone component, (4aS,7S,7aR)-nepetalactone, did not produce iridodial, they did convert ∾75% of this compound to the corresponding dihydronepetalactone, and wildC. oculatamales collected in early spring contained traces of this dihydronepetalactone. These findings are consistent with the hypothesis thatChrysopamales feed on oviparae (the late-season pheromone producing stage of aphids) to obtain nepetalactol as a precursor to iridodial. In the spring, however, wildC. oculatamales produce less iridodial than do males collected later in the season. Therefore, we further hypothesize that AsianChrysopaeatA. polygamato obtain iridoid precursors in order to make their pheromone, and that other iridoid-producing plants elsewhere in the world must be similarly usurped by maleChrysopaspecies to sequester pheromone precursors.


2015 ◽  
Author(s):  
Jeffrey R Aldrich ◽  
Kamal Chauhan ◽  
Qing-He Zhang

Green lacewings (Neuroptera: Chrysopidae) are voracious predators of aphids and other small, soft-bodied insects and mites. Earlier, we identified the first lacewing pheromone from field-collected males of the goldeneyed lacewing, Chrysopa oculata Say; (1R,2S,5R,8R)-iridodial is released from thousands of microscopic dermal glands on the abdominal sternum of males, along with comparable amounts of nonanal, nonanol and nonanoic acid. Iridodial-baited traps attract C. oculata and other Chrysopa spp. males into traps, while females come to the vicinity of, but do not usually enter baited traps. Despite their healthy appearance, normal fertility and usual amounts of C9 compounds, laboratory-reared C. oculata males do not produce iridodial. However, we observed that goldeneyed lacewing males caught alive in iridodial-baited traps sometimes try to eat the lure, and in Asia Chrysopa spp. males reportedly eat the native plant, Actinidia polygama (Siebold & Zucc.) Maxim. (Actinidiaceae) to obtain the iridoid, neomatatabiol. These observations prompted us to investigate why laboratory-reared Chrysopa green lacewings do not produce iridodial. Lacewing adult males fed various monoterpenes reduced carbonyls to alcohols and saturated double bonds, but did not convert these compounds to iridodial. Males fed the bicyclic iridoid aphid pheromone component, (4aS,7S,7aR)-nepetalactone, converted ~75% to dihydronepetalactone, but did not produce iridodial; however, wild C. oculata males collected in May often contained traces of dihydronepetalactone. On the other hand, adult males fed the second common aphid pheromone component, (1R,4aS,7S,7aR)-nepetalactol, converted this compound to iridodial. In California the peak late-season attraction of green lacewings to nepetalactol (the lactone is unattractive) occurs at least a month earlier than the peak in aphid oviparae (the pheromone producing morph of aphids), consistent with the hypothesis that Chrysopa males feed on oviparae to obtain nepetalactol as a precursor to iridodial. Adult males from laboratory-reared C. oculata larvae fed nepetalactol failed to produce iridodial, and wild C. oculata males collected early in the spring produce less iridodial than males collected later in the season. Therefore, we further hypothesize that Asian Chrysopa eat A. polygama to obtain iridoid precursors in order to make their pheromone, and that other iridoid-producing plants elsewhere in the world must be similarly usurped by male Chrysopa species to sequester pheromone precursors. Whether or not sequestration of iridodial precursors from oviparae and/or iridoid-containing plants is truly the explanation for lack of pheromone in laboratory-reared Chrysopa awaits further research .



2015 ◽  
Author(s):  
Jeffrey R Aldrich ◽  
Kamal Chauhan ◽  
Qing-He Zhang

Green lacewings (Neuroptera: Chrysopidae) are voracious predators of aphids and other small, soft-bodied insects and mites. Earlier, we identified the first lacewing pheromone from field-collected males of the goldeneyed lacewing, Chrysopa oculata Say; (1R,2S,5R,8R)-iridodial is released from thousands of microscopic dermal glands on the abdominal sterna of males, along with comparable amounts of nonanal, nonanol and nonanoic acid. Iridodial-baited traps attract C. oculata and other Chrysopa spp. males into traps, while females come to the vicinity of, but do not usually enter baited traps. Despite their healthy appearance, normal fertility and usual amounts of C9 compounds, laboratory-reared C. oculata males do not produce iridodial. However, we observed that goldeneyed lacewing males caught alive in iridodial-baited traps sometimes try to eat the lure, and in Asia Chrysopa spp. males reportedly eat the native plant, Actinidia polygama (Siebold & Zucc.) Maxim. (Actinidiaceae) to obtain the iridoid, neomatatabiol. These observations prompted us to investigate why laboratory-reared Chrysopa green lacewings do not produce iridodial. Lacewing adult males fed various monoterpenes reduced carbonyls to alcohols and saturated double bonds, but did not convert these compounds to iridodial. Males fed the bicyclic iridoid aphid pheromone component, (4aS,7S,7aR)-nepetalactone, converted ~75% to dihydronepetalactone, but did not produce iridodial; however, wild C. oculata males collected in May often contained traces of dihydronepetalactone. On the other hand, adult males fed the second common aphid pheromone component, (1R,4aS,7S,7aR)-nepetalactol, converted this compound to iridodial. In California the peak late-season attraction of green lacewings to nepetalactol (the lactone is unattractive) occurs at least a month earlier than the peak in aphid oviparae (the pheromone producing morph of aphids), consistent with the hypothesis that Chrysopa males feed on oviparae to obtain nepetalactol as a precursor to iridodial. Adult males from laboratory-reared C. oculata larvae fed nepetalactol failed to produce iridodial, and wild C. oculata males collected early in the spring produce less iridodial than males collected later in the season. Therefore, we further hypothesize that Asian Chrysopa eat A. polygama to obtain iridoid precursors in order to make their pheromone, and that other iridoid-producing plants elsewhere in the world must be similarly usurped by male Chrysopa species to sequester pheromone precursors. Whether or not sequestration of iridodial precursors from oviparae and/or iridoid-containing plants is truly the explanation for lack of pheromone in laboratory-reared Chrysopa awaits further research .



2015 ◽  
Author(s):  
Jeffrey R Aldrich ◽  
Kamal Chauhan ◽  
Qing-He Zhang

Green lacewings (Neuroptera: Chrysopidae) are voracious predators of aphids and other small, soft-bodied insects and mites. Earlier, we identified the first lacewing pheromone from field-collected males of the goldeneyed lacewing, Chrysopa oculata Say; (1R,2S,5R,8R)-iridodial is released from thousands of microscopic dermal glands on the abdominal sterna of males, along with comparable amounts of nonanal, nonanol and nonanoic acid. Iridodial-baited traps attract C. oculata and other Chrysopa spp. males into traps, while females come to the vicinity of, but do not usually enter baited traps. Despite their healthy appearance, normal fertility and usual amounts of C9 compounds, laboratory-reared C. oculata males do not produce iridodial. However, we observed that goldeneyed lacewing males caught alive in iridodial-baited traps sometimes try to eat the lure, and in Asia Chrysopa spp. males reportedly eat the native plant, Actinidia polygama (Siebold & Zucc.) Maxim. (Actinidiaceae) to obtain the iridoid, neomatatabiol. These observations prompted us to investigate why laboratory-reared Chrysopa green lacewings do not produce iridodial. Lacewing adult males fed various monoterpenes reduced carbonyls to alcohols and saturated double bonds, but did not convert these compounds to iridodial. Males fed the bicyclic iridoid aphid pheromone component, (4aS,7S,7aR)-nepetalactone, converted ~75% to dihydronepetalactone, but did not produce iridodial; however, wild C. oculata males collected in May often contained traces of dihydronepetalactone. On the other hand, adult males fed the second common aphid pheromone component, (1R,4aS,7S,7aR)-nepetalactol, converted this compound to iridodial. In California the peak late-season attraction of green lacewings to nepetalactol (the lactone is unattractive) occurs at least a month earlier than the peak in aphid oviparae (the pheromone producing morph of aphids), consistent with the hypothesis that Chrysopa males feed on oviparae to obtain nepetalactol as a precursor to iridodial. Adult males from laboratory-reared C. oculata larvae fed nepetalactol failed to produce iridodial, and wild C. oculata males collected early in the spring produce less iridodial than males collected later in the season. Therefore, we further hypothesize that Asian Chrysopa eat A. polygama to obtain iridoid precursors in order to make their pheromone, and that other iridoid-producing plants elsewhere in the world must be similarly usurped by male Chrysopa species to sequester pheromone precursors. Whether or not sequestration of iridodial precursors from oviparae and/or iridoid-containing plants is truly the explanation for lack of pheromone in laboratory-reared Chrysopa awaits further research .



2008 ◽  
Vol 34 (12) ◽  
pp. 1575-1583 ◽  
Author(s):  
Sarah Y. Dewhirst ◽  
Michael A. Birkett ◽  
Jean D. Fitzgerald ◽  
Alex Stewart-Jones ◽  
Lester J. Wadhams ◽  
...  


1991 ◽  
Vol 123 (6) ◽  
pp. 1209-1218 ◽  
Author(s):  
G.G. Grant ◽  
B. Pendrel ◽  
K.N. Slessor ◽  
X.Z. Meng ◽  
W.E. Miller

AbstractMoths of the genus Pseudexentera are early-season fliers that include three species of economic importance: P. spoliana (Clemens) on oak (Quercus), P. oregonana (Walsingham) on aspen (Populus), and P. mali Freeman on apple (Malus). GC and GC/MS analysis, EAG and behavioral bioassays, and field tests confirmed that Z10-16:Ac is an attractive sex pheromone component of female P. spoliana. Capillary GC analysis supported by GC/MS also indicated the presence of 16:Ac, Z10-16:OH, and 16:OH in pheromone extracts and there was tentative GC evidence for Z12-16:Ac. However, addition of these compounds to Z10-16:Ac in various blends did not enhance male attraction. The major sex pheromone component of female P. oregonana is Z8-14:Ac. There was also GC and GC/MS evidence for Z8-14:OH and tentative GC evidence for 14:Ac in the pheromone of this species. Their addition to Z8-14:Ac failed to increase moth catches in baited traps. Pseudexentera mali males were attracted by Z,Z-8,10-16:Ac, a previously reported sex pheromone of this species. Pheromone lures targeted for each species were not cross-attractive.



2015 ◽  
Vol 41 (6) ◽  
pp. 550-556 ◽  
Author(s):  
Sándor Koczor ◽  
Ferenc Szentkirályi ◽  
John A. Pickett ◽  
Michael A. Birkett ◽  
Miklós Tóth


2013 ◽  
Vol 39 (10) ◽  
pp. 1263-1272 ◽  
Author(s):  
Rafael Gago ◽  
Jeremy D. Allison ◽  
J. Steven McElfresh ◽  
Kenneth F. Haynes ◽  
Jessica McKenney ◽  
...  


2005 ◽  
Vol 31 (3) ◽  
pp. 621-646 ◽  
Author(s):  
A. M. El-Sayed ◽  
A. R. Gibb ◽  
D. M. Suckling ◽  
B. Bunn ◽  
S. Fielder ◽  
...  


Author(s):  
Wei-Kang Han ◽  
Yi-Lin Yang ◽  
Yu-Xiao Si ◽  
Zhi-Qiang Wei ◽  
Si-Ruo Liu ◽  
...  


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