5 × 10−3; diluted in paraffin; v/v) was added to a wick Five min

5 × 10−3; diluted in paraffin; v/v) was added to a wick. Five minutes later the wick was enclosed in an oven bag as described before and scent was subsequently collected for 2 min (two replicates). All samples collected were kept frozen (−20 °C)

until analysis. For identification of trapped volatiles, headspace samples were analysed on a Varian Saturn 2000 mass spectrometer coupled to a Varian 3800 Apitolisib gas chromatograph (GC) equipped with a 1079 injector (Varian Inc., Palo Alto, CA, USA), which had been fitted with the ChromatoProbe kit (Amirav and Dagan, 1997 and Dötterl et al., 2005a). Samples were directly inserted in the injector by means of the ChromatoProbe and analysed by thermal desorption. For all samples, the injector split vent was opened and the injector heated to 40 °C to flush any air from the system. The split vent was closed after 2 min, and the injector was heated at a rate of 200 °C/min to 200 °C, then held at 200 °C for 4.2 min, after which the split vent was opened and the injector cooled down. Separations were

achieved with a fused silica column ZB-5 (5% phenyl polysiloxane; 60 m long, inner diameter 0.25 mm, film thickness 0.25 μm, Phenomenex). Electronic flow control was used to maintain a constant helium carrier gas flow of 1.0 mL min−1. The GC oven temperature was held for 7 min Metabolism inhibitor at 40 °C, then increased by 6 °C per min to 250 °C and held for 1 min. The interface to the mass spectrometer worked at 260 °C and the ion trap at 175 °C. Mass spectra were

taken at 70 eV (in EI mode) with a scanning speed of 1 scan s−1 from m/z 30 to 350. The GC–MS data were processed using the Saturn Software package 5.2.1. Identification of compounds was carried out using the NIST 08, Wiley 7, and Adams 2007 mass spectral data bases, or the data base provided in MassFinder NADPH-cytochrome-c2 reductase 3, and confirmed by comparison of retention times with published data (Adams, 2007). Structure assignment of individual components was confirmed by comparison of both mass spectra and GC retention times with those of authentic standards. To determine the total amount of scent trapped, known amounts of monoterpenes, aliphatics, and aromatics were injected into the GC–MS system. Mean peak areas of these compounds were used to determine the total amount of scent (for more details see Dötterl et al., 2005a). By applying this method, the mean values (two replicates) for the amount of scent trapped from the wicks used for bioassays (1:1:1 diluted in paraffin, at overall 0.5 × 10−3; see below) were determined to be 2721 ng per hour of 4-oxoisophorone (extrapolated based on the 2 min collections), 229 ng of (E)-cinnamaldehyde, and 2 ng of (E)-cinnamyl alcohol. These differences in trapping/emission rates have to do with methodological/technical issues, such as the solubility in paraffin and the vapour pressure of the compounds.

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