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  • 1
    Electronic Resource
    Electronic Resource
    The effect of host spatial distribution on patterns of parasitism by Nasonia vitripennis (1987)
    Springer
    Entomologia experimentalis et applicata 44 (1987), S. 169-175 
    Details
    ISSN: 1570-7458
    Keywords: Hymenoptera ; Pteromalidae ; Nasonia vitripennis ; Diptera ; Calliphora sp. ; spatial distribution ; parasitism ; aggregation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Description / Table of Contents: Résumé Nous avons examiné les effets de différents niveaux d'agrégation des hôtes (pupes de Calliphora) sur l'efficacité parasitaire de Nasonia vitripennis. Une augmentation de l'agrégation des pupes a diminué le nombre d'hôtes parasités bien que le nombre de pupes attaquées ait été peu modifié. Cette différence a été attribuée à un accroissement des interactions comportementales entre les parasitoïdes et à une tendance au superparasitisme plus élevée lors des distributions les plus agrégatives. Plus les hôtes étaient concentrés, moins l'effectif de parasitoïdes achevant leur développement et émergeant était important. La fréquence des males a augmenté avec la concentration des pupes. Nous avons estimé que les facteurs déterminants ont été les interactions comportementales entre femelles et leur aptitude à modifier le taux sexuel de leur descendance immédiate. Nous en avons conclu que N. vitripennis est peut-être mieux adaptée aux populations d'hôtes distribuées au hasard, type de distribution le plus vraisemblable dans les populations naturelles.
    Notes: Abstract Patterns of parasitism of Calliphora sp. pupae by Nasonia vitripennis (Walker) (Hymenoptera: Pteromalidae) are explored under various conditions of host aggregation. Increasing the hosts' spatial aggregation decreased the number of hosts actually parasitised but had no significant effect on the total number of hosts attacked. Increasing host aggregation also resulted in a smaller parasitoid population with a more male biased sex ratio.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00367626
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  • 2
    Electronic Resource
    Electronic Resource
    Nest plundering allomones of the fire beeTrigona (Oxytrigona) mellicolor (1988)
    Springer
    Journal of chemical ecology 14 (1988), S. 495-501 
    Details
    ISSN: 1573-1561
    Keywords: Fire bee ; Trigona (Oxtrigona) mellicolor ; Trigona (Oxtrigona) tataira ; honeybee ; Apis mellifera ; Hymenoptera ; Apidae ; mandibular gland secretion ; allomone ; nest plundering ; diketones ; (E)-3-heptene-2,5-dione ; (E)-3-nonene-2,5-dione
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Ten volatile compounds derived from the cephalic glands of the fire beeTrigona (Oxytrigona)mellicolor were bioassayed for possible allomonal activities facilitating nest plundering. Two diketones, (E)-3-heptene-2,5-dione and (E)-3-nonene-2,5-dione, caused the honeybeeApis mellifera to display avoidance behavior and reduced defensive behavior. These diketones are produced in relatively large quantities in fire-bee cephalic glands.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01013901
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  • 3
    Electronic Resource
    Electronic Resource
    Venom chemistry of ants in the genusMonomorium (1982)
    Springer
    Journal of chemical ecology 8 (1982), S. 285-300 
    Details
    ISSN: 1573-1561
    Keywords: Monomorium spp. ; Hymenoptera ; Formicidae 2,5-dialkylpyrrolidines ; ant venom alkaloids ; methoxymercuration-demercuration ; chemotaxonomy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract A comparative analysis of the venomous alkaloids produced by ant species in the subgenusMonomorium of the genusMonomorium has been undertaken. All species produce mixtures of unsymmetricaltrans-2,5-dialkylpyrrolidines, but the proportions of the constituents may vary considerably between species. All alkaloids contain both C6 and C9 side chains which are present as C9-saturated. C6-monounsaturated, and both C6-and C9-monounsaturated dialkylpyrrolidines. The structure of 2-(1-hex-5-enyl)-5-(1-non-8-enyl)pyrrolidine, a previously undescribed alkaloid, was proved by unambiguous synthesis after the location of the double bonds was established by the methoxymercuration-demercuration followed by mass spectrometry. The possible chemotaxonomic significance of the mixtures of venomous alkaloids produced by these species ofMonomorium is discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00984024
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  • 4
    Electronic Resource
    Electronic Resource
    Chemistry of venom alkaloids in the ant genusMegalomyrmex (1991)
    Springer
    Journal of chemical ecology 17 (1991), S. 1897-1908 
    Details
    ISSN: 1573-1561
    Keywords: Megalomyrmex ; Hymenoptera ; Formicidae ; venom ; alkaloids ; ants ; trans-2,5-dialkylpyrrolidine ; 3,5-dialkylpyrrolizidine ; Hofmann degradation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Chemical analyses of three species in the Neotropical ant genusMegalomyrmex have identified this taxon as the third myrmicine genus to produce alkaloids as major venom products. Workers ofM. leoninus and workers and ergatoids ofM. goeldii produce one or more of fourtrans-2,5-dialkylpyrrolidines previously identified in other myrmicine genera.M. modestus, on the other hand, is distinctive in producing the novel alkaloid (5E,8E)-3-butyl-5-hexylpyrrolizidine (5d), whose structure was established using a micro-Hofmann degradation sequence. The relationship ofMegalomyrmex to other alkaloid-producing ant genera is discussed along with the possible chemotaxonomic significance of the analyzed species when viewed in terms of the recognized species groups in this genus.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00993736
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  • 5
    Electronic Resource
    Electronic Resource
    Chemistry of cephalic secretion of fire beeTrigona (Oxytrigona) tataira (1984)
    Springer
    Journal of chemical ecology 10 (1984), S. 451-461 
    Details
    ISSN: 1573-1561
    Keywords: Fire bee ; Trigona (Oxytrigona) tataira ; Hymenoptera ; Apidae ; mandibular gland secretion ; enediones ; monoketones ; carboxylic esters ; hydrocarbons ; E-3-hepten-2,5-dione ; E-3-nonen-2,5-dione
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Analysis of the volatile compounds derived from cephalic glands of the fire beeTrigona (Oxytrigona) tataira by GC-MS was undertaken. The following compounds were readily identified: hydrocarbons:n-C11H24,n-C13H28,n-C14H30,n-C15H32,n-C17H36,n-C23H48,n-C15H30,n-C17H34,n-C21 H42, andn-C23H46; carboxylic acids: palmitic acid, linoleic acid, linolenic acid, stearic acid, and oleic acid; carboxylic esters: dodecyl acetate, tetradecyl acetate, hexadecyl acetate, octadecyl acetate, and dodecyl decanoate; monoketones: 5-hepten-2-one, 3-hepten-2-one, 2-heptanone, and 5-nonen-2-one. Two major components of the mixture were identified asE-hepten-2,5-dione andE-3-nonen-2,5-dione. Structures of these novel compounds were suggested by their GC-MS behavior and the GC-MS behavior of their dimethoximes and proved by comparison with authentic synthetic samples. Trace amounts of the corresponding Z isomers and the saturated analogs, heptan-2,5-dione and nonan-2,5-dione, were also found. The possible functions of these glandular constituents are discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00988091
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  • 6
    Electronic Resource
    Electronic Resource
    3-Hexyl-5-Methylindolizidine Isomers from Thief Ants, Solenopsis (Diplorhoptrum) Species (1998)
    Springer
    Journal of chemical ecology 24 (1998), S. 933-943 
    Details
    ISSN: 1573-1561
    Keywords: Venom ; alkaloids ; Solenopsis (Diplorhoptrum) ; indolizidine ; chemotaxonomy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The venom alkaloids from the workers of nine collections of Solenopsis (Diplorhoptrum) from California contain either (5E,9E)-3-hexyl-5-methylindolizidine (1c) or (5Z,9E)-3-hexyl-5-methylindolizidine (1d) along with cis-2-methyl-6-nonylpiperidine. The structures of these compounds were determined from their mass spectra and by comparison of their GC-FTIR spectra with those of a synthetic mixture. In view of the facts that a third diastereomer of 3-hexyl-5-methylindolizidine had been reported in previous collections of Solenopsis (Diplorhoptrum) queens from Puerto Rico, and that indolizidines along with other ant venom alkaloids are sequestered by amphibians, the determination of species in this difficult group of ants is significant. In particular, the chemotaxonomic value of the stereochemistry of these venom alkaloids is discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1022381719471
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  • 7
    Electronic Resource
    Electronic Resource
    Chemistry of venom alkaloids in the antMegalomyrmex foreli (Myrmicinae) from Costa Rica (1991)
    Springer
    Journal of chemical ecology 17 (1991), S. 2507-2518 
    Details
    ISSN: 1573-1561
    Keywords: Megalomyrmex ; Hymenoptera ; Myrmicinae ; venom ; alkaloids ; ants ; pyrrolines ; alarm behavior ; stridulation ; toxicity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Chemical analysis of the venom of the myrmicine antMegalomyrmex foreli from Costa Rica revealed the presence of four major alkaloidal components. Two of these, 2-butyl-5-(E, 1-heptenyl)-5-pyrroline (3) and 2-butyl-5-(E, E, 1,3-heptadienyl)-5-pyrroline (4), constitute a new functional class of ant venom alkaloids, whose structures were assigned from their spectral and chemical behavior and unambiguous syntheses. The function of these compounds is suggested by field observations of the behavior ofM. foreli, its sting morphology, and the relative toxicity of 3 and 4 against termite workers.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00994598
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  • 8
    Electronic Resource
    Electronic Resource
    Chemistry of venom alkaloids in someSolenopsis (Diplorhoptrum) species from Puerto Rico (1996)
    Springer
    Journal of chemical ecology 22 (1996), S. 1221-1236 
    Details
    ISSN: 1573-1561
    Keywords: Venom ; alkaloids ; Solenopsis ; Puerto Rico
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract A number of 15-carbon alkaloids have been identified in venom extracts of four Puerto Rican species of ants in the genusSolenopsis (Diplorhoptrum). Workers of a species from El Verde produced thecis andtrans isomers of 2-methyl-6-nonylpiperidine with the latter isomer predominating. The same compounds were identified in queens of a species from Río Grande, but in this species no alkaloids were detected in worker extracts. Workers of aDiplorhoptrum species collected on Mona Island produced primarily atrans-2-methyl-6-(Z-4-nonenyl)piperidine,3, with smaller amounts of thecis isomer, whereas the major compound found in the queens of the same species on Mona Island was (5Z,9Z)-3-hexyl-5-methylindolizidine, identical with the alkaloid produced by queens of a species collected on Cabo Rojo. Surprisingly, workers of the Cabo Rojo species produced (5Z,9Z)- and (5E,9E)-3-butyl-5-propylindolizidine (4 and5, respectively) reported earlier as the 223AB indolizidines from skins of dendrobatid frogs. The possible significance of the qualitative and quantitative differences in the venom alkaloids synthesized by queens and workers is discussed as is the possibility that ants containing such alkaloids may serve as a dietary source for the skin alkaloids used by certain frogs in chemical defense.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02266962
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