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Nestmate recognition

Polistes dominulus W-CW Nestmate recognition cues 7-Methylnonacosane 73,11-methylnona-cosane 74, (1 lZ)-nonacos-l l-ene 75, (llZ)-hentriacont-ll-ene 76, (9Z)-nonacos-9-ene 77 [116]... [Pg.169]

Workers are often cited as the source of nestmate or kin recognition cues (e.g., [115]). Many GC analysis studies have shown that the cuticular hydrocarbon profiles are different between nestmates and non-nestmates. However, only recently have specific hydrocarbons, 7-methylnonacosane 73,11-methyl-nonacosane 74, (llZ)-nonacos-ll-ene 75, (llZ)-hentriacont-ll-ene 76, and (9Z)-nonacos-9-ene 77, been shown to mediate nestmate recognition in the paper wasp, Polistes dominulus [116]. [Pg.171]

Vander Meer RK, Morel L (1998) Nestmate recognition in ants. In Vander Meer RK, Breed MD, Espelie KE, Winston ML (eds) Pheromone communication in social insects ants, wasps, bees and termites. Westview Press, Boulder, Colorado, p 79... [Pg.178]

Breed, M.D., Diaz, P.H. and Lucero, K.D. (2004) Olfactory information processing in honey bee, Apis mellifera, nestmate recognition. Anim. Behav. 68, 921-928. [Pg.176]

Gamboa, J.G., Reeve, H.K., Ferguson, I.D. and Wacker, T.L. (1986) Nestmate recognition in social wasps the origin and acquisition of recognition odours. Anim. Behav. 34, 685-695. [Pg.176]

Vander Meer RK, Morel L (1998) Nestmate recognition in ants. In Vander Meer RK,... [Pg.175]

Nestmate recognition ant cuticular hydrocarbons Wagner etal. (2000) Lahav etal. (2001) ... [Pg.324]

Chen J. S. C. and Nonacs P. (2000) Nestmate recognition and intraspecific aggression... [Pg.335]

Clement J.-L. and Bagneres A.-G. (1998) Nestmate recognition in termites, pp. 126-155, In eds R. K. Vander Meer, M. Breed, M. Winston and K. Espelie, Pheromone Communication in Social Insects Ants, Wasps, Bees, and Termites, Westview Press, Boulder, CO. [Pg.336]

Hernandez J. V., Lopez H. and Jaffe K. (2002) Nestmate recognition signals of the leafcutting ant Atta laevigata. J. Insect Physiol. 48, 287-295. [Pg.337]

Lenoir A., Cuisset D. and Hefetz A. (2001a) Effects of social isolation on hydrocarbon pattern and nestmate recognition in the ant Aphaenogaster senilis (Hymenoptera, Formicidae). Insectes Soc. 48, 101-109. [Pg.338]

Liang D. and Silverman J. (2000) You are what you eat diet modifies cuticular hydrocarbons and nestmate recognition in the Argentine ant, Linepithema humile. Naturwissenschaften 87, 412-416. [Pg.338]

Ruther J., Sieben S. and Schricker B. (2002) Nestmate recognition in social wasps manipulation of hydrocarbon profiles induces aggression in the European hornet. Naturwissenschaften 89, 111-114. [Pg.339]

Soroker V., Vienne C., Nowbahari E., and Hefetz A. (1994) The postpharyngeal gland as a gestalt organ for nestmate recognition in the ant Cataglyphis niger. Naturwissenschaften 81, 510-513. [Pg.339]

Wagner D., Tissot M., Cuevas W. and Gordon D. M. (2000) Harvester ants utilize cuticular hydrocarbons in nestmate recognition. J. Chem. Ecol. 26, 2245-2257. [Pg.340]

Zanetti P, Dani F. R., Destri S., Fanelli D., Massolo A., Moneti G., Pieraccini G. and Turillazzi S. (2001) Nestmate recognition in Parischnogaster striatula (Hymenoptera Stenogastrinae), visual and olfactory recognition cues. J. Insect Physiol. 47, 1013— 1020. [Pg.340]

The long-chain hydrocarbons of insects play central roles in the waterproofing of the insect cuticle and function extensively in chemical communication where relatively non-volatile chemicals are required. The recognition of the critical roles that hydrocarbons serve as sex pheromones, kairomones, species and gender recognition cues, nestmate recognition, dominance and fertility cues, chemical mimicry, primer pheromones and task-specific cues has resulted in an explosion of new information in the past several decades, and, indeed, served as the impetus for this book. [Pg.3]

Bonavita-Cougourdan, A., Clement, J.L. and Lange, C. (1987). Nestmate recognition the role of cuticular hydrocarbons in the ant Camponotus vagus Scop../. Entomol. ScL, 22, 1-10. [Pg.12]

Morel, L., Vander Meer, R.K. and Lavine, B. K. (1988). Ontogeny of nestmate recognition cues in the red carpenter ant (Camponotus floridanus) Behavioral and chemical evidence for the role of age and social experience. Behav. Ecol. Sociobiol., 22,175-183. [Pg.17]

Dani, F., Fratini, S. and Turillazzi, S. (1996a). Behavioural evidence for the involvement of Dufour s gland secretion in nestmate recognition in the social wasp Polistes dominulus (Hymenoptera Vespidae). Behav. Ecol. Sociobiol., 38, 311-319. [Pg.92]

Dani, F., Morgan, E.D. and Turillazzi, S. (1996b). Dufour gland secretion of Polistes wasps chemical composition and possible involvement in nestmate recognition (Hymenoptera Vespidae)../. Insect Physiol., 42, 541-548. [Pg.92]

Vander Meer, R. K. and Morel, L. (1998). Nestmate recognition in ants. In Pheromone Communication in Social Insects. Ants, Wasps, Bees and Termites, ed. R. K. Vander Meer, M. D. Breed, K. E. Espelie and M.L. Winston. New York Westview Press, pp. 79-103. [Pg.99]

Lorenzi, M.-C., Bagneres, A-G., Clement, J.-L and Turillazzi, S. (1997). Polistes biglumis bimaculatus epicuticular hydrocarbons and nestmate recognition (Hymenoptera Vespidae). Insect Soc., 44, 123-138. [Pg.158]

Torres, C. W., Brandt, M. and Tsutsui, N.D. (2007). The role of cuticular hydrocarbons as chemical cues for nestmate recognition in the invasive Argentine ant (Linepithema humile). Insect Soc., 54, 363-373. [Pg.162]

The external cuticle of insects is covered by a waxy layer composed of mixtures of hydro-phobic lipids that include long-chain alkanes, alkenes, wax esters, fatty acids, alcohols, aldehydes, and sterols. The primary purpose of this layer is to maintain water balance and prevent desiccation, as described in Chapter 6, but many of the cuticular lipid components have important secondary roles as intraspecific contact chemical signals (pheromones). These roles include species and sex recognition during reproductive interactions, and nestmate recognition and other colony organization functions in social insects. Thus, these compounds are essential mediators of insect behaviors. Cuticular compounds are also exploited by parasitoids and predators as interspecific contact cues (kairomones) to aid in host location. [Pg.163]

Akino, T., Yamamura, K., Wakamura, S. and Yamaoka, R. (2004). Direct behavioral evidence for hydrocarbons as nestmate recognition cues in Formica japonica (Hymenoptera Formicidae). Appl. Entomol. Zool., 39, 381-387. [Pg.181]

In addition to the Drosophila sex pheromone CHCs mentioned above, it is well known that CHCs are used by ants for various chemical communications nestmate recognition, caste discrimination, etc. (see related chapters). In various ant species, chemical analysis of the body surface materials suggested that the colony-specific blends of a multi-component CHC mixture act as the nestmate-discriminative pheromone (Bonavita-Cougourdan et al., 1987 Yamaoka, 1990 Howard, 1993 Vander Meer and Morel, 1998 Howard and Blomquist, 2005). In a Japanese carpenter ant, Camponotus japonicus, the CHC pheromone, consisting of 18 CHC components of 20-40 carbons, is used as a chemical cue for nestmate and non-nestmate discrimination (Yamaoka, 1990). Because of the antennation behavior for inspecting encountered ants, the CHC-sensitive sensillum was expected to be discovered on the antenna. [Pg.209]

CHCs were proposed as the chemical sign for nestmate recognition (Bonavita-Cougourdan... [Pg.215]

Blomquist, 2005). The colony-specific CHC profiles could be detected even by a single sweep of their antennae (Wilson, 1971 Tanner, 2008). Thus, based on the chemical signatures of CHC mixtures, nestmate recognition underlies various social behaviors of ants. The hypothesis that CHCs play essential roles in the social behaviors of ants has been supported by experimental evidence through a variety of behavioral bioassays or correlation studies in which cuticular compounds are removed and reapplied via solvent extraction (Bonavita-Cougourdan et al., 1987 Howard, 1993 Vander Meer and Morel, 1998 Breed, 1998 Martin et al., 2008a, b Guerreri and d Ettore, 2008). This hypothesis was further... [Pg.215]

See other pages where Nestmate recognition is mentioned: [Pg.57]    [Pg.58]    [Pg.328]    [Pg.338]    [Pg.8]    [Pg.8]    [Pg.80]    [Pg.81]    [Pg.84]    [Pg.86]    [Pg.88]    [Pg.158]    [Pg.214]    [Pg.216]   
See also in sourсe #XX -- [ Pg.3 , Pg.8 , Pg.17 , Pg.80 , Pg.81 , Pg.84 , Pg.86 , Pg.88 , Pg.92 , Pg.98 , Pg.158 , Pg.162 , Pg.163 , Pg.181 , Pg.209 , Pg.214 , Pg.215 , Pg.216 , Pg.217 , Pg.222 , Pg.223 , Pg.224 , Pg.225 , Pg.226 , Pg.227 , Pg.228 , Pg.229 , Pg.230 , Pg.231 , Pg.232 , Pg.233 , Pg.234 , Pg.235 , Pg.237 , Pg.238 , Pg.239 , Pg.240 , Pg.241 , Pg.242 , Pg.243 , Pg.253 , Pg.274 , Pg.298 , Pg.309 , Pg.319 , Pg.320 , Pg.322 , Pg.477 ]



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