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Field Response of Male Pine Sawflies, Neodiprion sertifer (Diprionidae), to Sex Pheromone Analogs in Japan and Sweden

Anderbrant, Olle (author)
Lund University,Lunds universitet,Funktionell zoologi,Biologiska institutionen,Naturvetenskapliga fakulteten,Functional zoology,Department of Biology,Faculty of Science,Department of Biology, Lund University
Löfqvist, Jan (author)
Swedish University of Agricultural Sciences, Alnarp,Department of Plant Protection Science, Swedish University of Agricultural Sciences, Alnarp
Hedenström, Erik (author)
Mid Sweden University,Mittuniversitetet,Institutionen för naturvetenskap, teknik och matematik (-2012)
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Bång, Joakim (author)
Mid Sweden University,Mittuniversitetet,Institutionen för naturvetenskap, teknik och matematik (-2012)
Tai, Akira (author)
Faculty of Science, Himeji Institute of Technology, Kanaji Kamigor, Japan,University of Hyogo
Högberg, Hans-Erik (author)
Mid Sweden University,Mittuniversitetet,Institutionen för naturvetenskap, teknik och matematik (-2012)
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 (creator_code:org_t)
2010-08-01
2010
English.
In: Journal of Chemical Ecology. - : Springer Science and Business Media LLC. - 0098-0331 .- 1573-1561. ; 36:9, s. 969-977
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The pine sawfly Neodiprion sertifer (Geoffroy) uses the acetate or propionate of (2S,3S,7S)-3,7-dimethyl-2-pentadecanol (diprionol) as pheromone components, with the (2S,3R,7R)-isomer being antagonistic, synergistic, or inactive according to the population tested. In this study, we tested the attraction of males to the acetates of three analogs of diprionol, each missing one methyl group, viz. (2S,7S)-7-methyl-2-pentadecanol, (2S,6S)-2,6-dimethyl-1-tetradecanol, and (2S,3S)-3-methyl-2-pentadecanol. None of the analogs alone, or in combination with diprionol acetate, was attractive in Sweden, even at 100 times the amount of diprionol acetate attractive to N. sertifer. In Japan, the acetate of (2S,3S)-3-methyl-2-pentadecanol attracted males when tested in amounts 10–20 times higher than the acetate pheromone component. The acetate esters of the (2S,3R)-analog and the (2S,3R,7R)-isomer of diprionol also were tested in combination with the pheromone compound (acetate ester). Both compounds caused an almost total trap-catch reduction in Sweden, whereas in Japan they appear to have relatively little effect on trap capture when added to diprionol acetate. Butyrate and iso-butyrate esters of diprionol were unattractive to N. sertifer in Sweden. In summary, there exists geographic variation in N. sertifer in responses to both diprionyl acetate and some of its analogs.

Subject headings

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)
NATURVETENSKAP  -- Biologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences (hsv//eng)
NATURVETENSKAP  -- Biologi -- Zoologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Zoology (hsv//eng)

Keyword

Chemistry
Kemi

Publication and Content Type

ref (subject category)
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