Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 1034
Function: getPubMedXML
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3152
Function: GetPubMedArticleOutput_2016
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
Long-range sex pheromones are generally considered to be a main cue for mate recognition in the order Hymenoptera. Although considerable attention has been given to the identification of semiochemicals in the superfamily Chalcidoidea, which comprises 19 families, no study has identified active components in a field bioassay. We herein report the sensitive and selective pheromone communication system of the Korean apricot wasp, Eurytoma maslovskii (Eurytomidae), whose larvae feed on Prunus mume seeds. Using gas chromatography coupled with electroantennographic detection (GC-EAD) and mass spectrometry (GC-MS), we detected 2,10-dimethyldodecyl propionate and 2,8-dimethyldecyl propionate in thoracic extracts of female E. maslovskii at a ratio of 8:2 as the active pheromone components. Field experiments showed that the attractive effect of the two compounds is highly enantioselective. Racemic 2,10-dimethyldodecyl propionate and 2,8-dimethyldecyl propionate were not attractive to E. maslovskii males. In bioassays with single enantiomers, the (2 S,10 R)-enantiomer was highly attractive to male wasps, and the (2 S,8 S)-enantiomer was also attractive, although to a lesser degree. No synergistic effect between (2 S,10 R)- and (2 S,8 S)-enantiomers was identified, and the (2 S,10 R)-enantiomer alone caught significantly more males than the natural pheromone extracts. The addition of other enantiomers to the (2 S,10 R)-isomer significantly decreased the attraction of conspecific males. In addition, a very low dose of synthetic pheromone attracted conspecific males, showing that both female signaling and male response traits may have evolved to contribute to species-specific sexual communication in this species.
Download full-text PDF |
Source |
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7314779 | PMC |
http://dx.doi.org/10.1038/s41598-020-67252-7 | DOI Listing |
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