Library

X
feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Trace co-attractants in synthetic sex lures for 22 noctuid moths (1982)
    Springer
    Cellular and molecular life sciences 38 (1982), S. 94-96 
    Details
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Trace components contributed significantly to the potency of synthetic sex attractant lures for males of many species of Noctuidae. Improved synthetic blends for 12 moths includingEuxoa ochrogaster andTrichoplusia ni, and new lure blends for 10 moths are described. In every case the trace constituents were structural analogs of the main lure components.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01944547
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 2
    Electronic Resource
    Electronic Resource
    Structure-activity relationships in sex attractants for north American noctuid moths (1982)
    Springer
    Journal of chemical ecology 8 (1982), S. 731-754 
    Details
    ISSN: 1573-1561
    Keywords: Alkenylcompounds ; pheromones ; chemotaxonomy ; decenyl dodecenyl ; tetradecenyl ; hexadecenyl ; trapping ; Lepidoptera ; Noctuidae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Sex attractants known for 145 species of noctuid moths have many common features both as to chemical constituents and to their relationships in blends. The great majority of constituents are straight-chain (Z)-alkenols, -alkenals, or -alkenyl acetates of even carbon number (10 through 16). The unsaturation is nonterminal in odd-numbered positions (5 through 11). In effective lures, these components are blended in specific ratios and the components in a sex pheromone or sex attractant blend are structurally related by “one-change” steps. This means that any blend component differs from one or more other components by a single structural alteration, such as a change in double bond position, or a change in carbon chain length, or a change in the oxygen function. For the few multicomponent systems known in detail, the central place in the “one-change” framework is occupied by the predominant blend component. Different patterns of occurrence of lure components occur in the subfamilies Acronictinae, Noctuinae, Hadeninae, Cuculliinae, Amphipyrinae, Heliothidinae, Plusiinae, Acontiinae, and Pantheinae, and some subfamilies are as yet without known lures. Some guiding principles for elucidation of blend compositions for unstudied species are presented; these guidelines can also be used in improvement of some synthetic blends of unsatisfactory quality.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00988315
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 3
    Electronic Resource
    Electronic Resource
    Triunsaturated hydrocarbons, sex pheromone components ofCaenurgina erechtea (1983)
    Springer
    Journal of chemical ecology 9 (1983), S. 1413-1423 
    Details
    ISSN: 1573-1561
    Keywords: Behavior ; Caenurgina erechtea (Cramer) ; forage looper ; Lepidoptera ; Noctuidae ; sex pheromone ; (Z,Z,Z)-3,6,9-eicosatriene ; (Z,Z,Z)-3,6,9-heneicosatriene ; flight tunnel
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract (Z,Z,Z)-3,6,9-Eicosatriene and (Z,Z,Z)-3,6,9-heneicosatriene have been identified as components of the sex pheromone of the noctuid,Caenurgina erechtea (Cramer), the forage looper. Structural assignments were made on the basis of spectroscopic and chromatographic data and were confirmed by comparison with synthetic material. Flight tunnel behavioral studies demonstrated that either component, when tested individually, would elicit wing fanning responses in males; however, mixtures of the two components increased this response and were essential for initiation of upwind flight and landing. In field experiments, traps baited with either component alone captured few or no adult forage looper males while those baited with both components captured several target males.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00990747
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 4
    Electronic Resource
    Electronic Resource
    9,11-Dodecadienyl alcohols, acetates, or aldehydes as synthetic chemical sex attractants for four Lepidoptera:Cosmopterix gemmiferella (Clemens),Dichrorampha simulana (Clemens),Tortricidia testacea (Packard), and anAncylis sp. (1985)
    Springer
    Journal of chemical ecology 11 (1985), S. 1341-1347 
    Details
    ISSN: 1573-1561
    Keywords: Sex attractant ; Cosmopterigidae ; Tortricidae ; Cosmopterix gemmiferella ; Dichrorampha simulana ; Tortricidia testacea ; Ancylis sp. ; (9Z)-9,11-dodecadienyl acetate ; (9E)-9,11-dodecadienyl acetate ; (9Z)-9,11-dodecadien-1-ol ; (9E)-9,11-dodecadien-1-ol ; (9Z)-9,11-dodecadienal ; (9E)-9,11-dodecadienal
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Four lepidoptera were lured to field traps containing various combinations of 9,11-dodecadienes with alcohol, acetate, or aldehyde functional groups. All species required two chemical components for best attraction.Cosmopterix gemmiferella was most responsive to a combination of (9Z)-9,11-dodecadienyl acetate and (9E)-9,11-dodecadienyl acetate in 2∶1 ratio;Dichrorampha simulana to (9E)-9,11-dodecadienyl acetate and (9E)-9,11-dodecadien-1-ol in 10∶1 ratio;Tortricidia testacea to (9Z)-9,11-dodecadienal and (9E)-9,11-dodecadienal in 10∶1 ratio; andAncylis sp. to (9Z)-9,11-dodecadienyl acetate and (9Z)-9,11-dodecadien-1-ol in 10∶1 ratio.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01012135
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 5
    Electronic Resource
    Electronic Resource
    Field trapping of threeEpinotia species with (Z,Z)-7,9-dodecadienyl acetate (Lepidoptera: Tortricidae) (1985)
    Springer
    Journal of chemical ecology 11 (1985), S. 1389-1398 
    Details
    ISSN: 1573-1561
    Keywords: (Z,Z)-7,9-Dodecadienyl acetate ; (Z,Z)-7,9-dodecadien-1-ol ; Epinotia silvertoniensis ; Epinotia criddleana ; Epinotia sp. ; Lepidoptera ; Tortricidae ; sex attractant
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Field survey of the geometrical isomers of 7,9-dodecadienyl alcohol, acetate, and aldehyde has resulted in attractants and inhibitors for three species of tortricid moths.Epinotia silvertoniensis and an undescribedEpinotia sp. were all attracted to (Z,Z)-7,9-dodecadienyl acetate. AnotherEpinotia sp. was attracted to (Z,Z)-7,9-dodecadienyl acetate and (Z,Z)-7,9-dodecadien-1-ol. Electroantennogram data and inhibition patterns for one of theEpinotia sp. are also reported. In addition,E. criddleana was attracted to lures containing (E)-9-dodecenyl acetate.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01012139
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 6
    Electronic Resource
    Electronic Resource
    Attraction of tortricid moths of subfamily olethreutinae to field traps baited with dodecadienes (1985)
    Springer
    Journal of chemical ecology 11 (1985), S. 217-230 
    Details
    ISSN: 1573-1561
    Keywords: Sex attractant ; Lepidoptera ; Tortricidae ; Olethreutinae ; 8,10-dodecadienes ; 7,9-dodecadienes ; field trapping
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract All four geometrical isomers of 7,9- and 8,10-dodecadienes with acetate, alcohol, and aldehyde functional groups were synthesized and field tested. The field survey produced sex attractant lures for 14 insect species. Species in the generaCydia, Grapholita, Eucosma, Pelochrista, Petrova, Phenta, Hedya, and Pseudosciaphila were captured. Defined lures were developed for some of the species captured. Gas chromatographie retention times for all geometrical isomers of 7,9- and 8,10-dodecadienes with acetate, alcohol, and aldehyde functional groups are reported. A study of the isomerization of 8,10-dodecadienyl acetates and aldehydes impregnated in rubber septa is reported.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00988204
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 7
    Electronic Resource
    Electronic Resource
    Optimized conditions for sex attractant trapping of male redbacked cutworm moths,Euxoa ochrogaster (Guenée) (1980)
    Springer
    Journal of chemical ecology 6 (1980), S. 585-591 
    Details
    ISSN: 1573-1561
    Keywords: Sex attractant ; trapping ; redbacked cutworm moth ; Euxoa ochrogaster ; Lepidoptera ; Noctuidae ; (Z)-5- and (Z)-7-dodecenyl acetates
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Mixtures of (Z)-5- and (Z)-7-dodecenyl acetates in ratios 〉100∶1 are powerful, specific sex attractants for redbacked cutworm male moths. Bioactive lures were produced by admixture of these pure compounds or through syntheses involving catalytic bond shifting. Best field trapping was obtained with 200∶1 (Z)-5∶(Z)-7 ratio, at lure doses (on rubber) of 0.1–2.0 mg, using cone swivel traps with 10- to 13-mm orifices, or Pherocon® 1-CP sticky traps, at a height of 50–90 cm. The pheromone traps were more efficient than large blacklight traps and captured the various morphological forms of the moth in similar ratios.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00987670
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 8
    Electronic Resource
    Electronic Resource
    Synthesis of sex pheromone components of the forest tent caterpillar,Malacosoma disstria (Hübner) and of the western tent caterpillar,Malacosoma californicum (Packard) (1981)
    Springer
    Journal of chemical ecology 7 (1981), S. 159-164 
    Details
    ISSN: 1573-1561
    Keywords: Synthesis ; isomers ; 5,7-dodecadienal ; sex pheromone ; Malacosoma disstria ; Malacosoma californicum ; Lepidoptera ; Lasiocampidae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract All four geometrical isomers of 5,7-dodecadien-1-ol have been stereoselectively synthesized by using Wittig condensation reactions. (5 Z,7E)-5,7-Dodecadien-1-ol and its corresponding aldehyde are components of the sex pheromone of the forest tent caterpillar. (5 E,7 Z)-5,7-Dodecadienal is a component of the pheromone of the western tent caterpillar. These compounds have been successfully tested in the field.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00988643
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 9
    Electronic Resource
    Electronic Resource
    Geometrical and positional isomerization of alkenyl acetates produced by hydrogenation of alkynyl acetates over palladium metal catalysts (1978)
    Springer
    Journal of chemical ecology 4 (1978), S. 657-663 
    Details
    ISSN: 1573-1561
    Keywords: Pheromone ; trans isomer ; cis isomer ; alkenyl acetate ; alkynyl acetate ; hydrogenation ; isomerization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Alkenyl acetates containing both geometrical isomers can be produced by a single controlled catalytic hydrogenation of the corresponding alkynyl acetate. The hydrogenation is capable of yielding formulations containing up to 60% trans isomer; the reduction is attended by positional isomerization in both geometrical isomers.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00990276
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 10
    Electronic Resource
    Electronic Resource
    Attraction and inhibition in moth species responding to sex-attractant lures containing Z-11-hexadecen-1-yl acetate (1977)
    Springer
    Journal of chemical ecology 3 (1977), S. 603-612 
    Details
    ISSN: 1573-1561
    Keywords: Eurois occulta ; Leucania commoides ; Scotogramma trifolii ; Crymodes devastator ; Mamestra configurata ; sex pheromones ; specificity ; Lepidoptera ; chemical communication
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Sex attractants for several sympatric noctuid moths required Z-11-hexadecen-1-yl acetate and additional olefinic compounds (coattractants) for effective, species-specific operation. In nearly all cases at least one of the coattractant compounds for each species functioned as a strong inhibitor of one or more of the other species in the group. It was concluded that species specificity in sex attractants can be achieved through conspecific coattractants which are at the same time transspecific inhibitors.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00989080
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...