Whether olfaction recognizes odorants by their shape, their molecular vibrations, or both remains an open and controversial question. A convenient way to address it is to test for odor character differences between deuterated and undeuterated odorant isotopomers, since these have identical ground-state conformations but different vibrational modes. In a previous paper (Franco et al. (2011) Proc Natl Acad Sci USA 108:9, 3797-802) we showed that fruit flies can recognize the presence of deuterium in odorants by a vibrational mechanism. Here we address the question of whether humans too can distinguish deuterated and undeuterated odorants. A previous report (Keller and Vosshall (2004) Nat Neurosci 7:4, 337-8) indicated that naive subjects are incapable of distinguishing acetophenone and d-8 acetophenone. Here we confirm and extend those results to trained subjects and gas-chromatography [GC]-pure odorants. However, we also show that subjects easily distinguish deuterated and undeuterated musk odorants purified to GC-pure standard. These results are consistent with a vibrational component in human olfaction.

No abstract

Take-down policy If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim.

The efficacy of an improved form of the mass‐trapping method for the control of the olive fruit fly, Bactrocera oleae (Gmelin) was tested for 4 years in a pilot test at Tanagra Voeotia, Greece. Improvements consisted of the extension of the active life of the toxic trap used, active life referring both to its attracting and killing properties, as well as in trap deployment, which combined efficacy and low cost. The method was compared to bait sprays applied from the ground, which constitutes the current standard method for the control of this pest. Both pest population density and fruit infestation levels, the main parameters used for the evaluation of the two methods were considerably lower during all 4 years of tests in the orchards protected by mass trapping compared with those in the orchards protected by bait sprays. Furthermore no complementary measures were required in the mass‐trapping orchards for acceptable crop protection, which was not the case under certain conditions, prior to the introduction of the recent improvements. The cost of the mass‐trapping method was approximately US$ 0.40 per tree per year compared with US$ 0.35 for bait sprays (figures of the Greek Ministry of Agriculture). However, the mass‐trapping method reduces the amount of insecticide used for olive protection by 99.5% (15 mg a.i. per tree per year as opposed to 3 g in the case of bait sprays). A considerable reduction in the cost of the mass‐trapping method is expected with the extension of its use and the mass production of materials used, especially traps.

Screening systems for ecdysteroid mimetic or antiecdysteroid substances in plant extracts or libraries of synthetic compounds are commonly based on the observation of morphological and/or growth responses in insect cell lines. Because these responses are slow and require careful monitoring, existing screening systems are considered limited regarding their applicability to analysis in high-throughput (HT) formats. Here we describe the generation of transformed silkmoth (Bombyx mori) cell lines that respond to the addition of ecdysone-like substances through the expression of the green fluorescent protein (GFP) and the appearance of green fluorescence. Because tests consist of three simple steps, i.e., 1) distribution of transformed cells in microtiter plates; 2) addition of compounds/extracts at different concentrations; and 3) quantification of fluorescence intensity by a fluorescence plate reader, they can be performed quickly and be easily adapted to a HT format. The generated reporter cell lines are used for the screening of extracts from available plant collections for the presence of compounds with ecdysone mimetic or antagonistic activities as well as for monitoring subsequent activity during enrichment and purification steps. The same cell lines are also used here for the determination of structure-activity relationships among available synthetic dibenzoylhydrazine derivatives. Finally, for the identified agonists, we show that their activity as determined by the cell-based screening assays parallels their bioactivity in growth inhibition and toxicity assays carried out on live insects.