Tandem mass spectrometry of organophosphate and carbamate pesticides

We present tandem quadrupole mass spectrometric data for 26 organophosphate and 16 carbamate pesticides. These data are of use in developing methods for screening samples for specific compounds (by selected reaction monitoring) or specific classes of compounds (by parent scans and neutral loss scans). Optimization of tandem mass spectrometry conditions for maximum sensitivity is also described.     

Interaural spectral asymmetry and sensitivity to interaural time differences

Listeners' ability to discriminate interaural time difference (ITD) changes in low-frequency noise was determined as a function of differences in the noise spectra delivered to each ear. An ITD was applied to Gaussian noise, which was bandpass filtered using identical high-pass, but different low-pass cutoff frequencies across ears. Thus, one frequency region was dichotic, and a higher-frequency region monotic. ITD thresholds increased as bandwidth to one ear (i.e., monotic bandwidth) increased, despite the fact that the region of interaural spectral overlap remained constant. Results suggest that listeners can process ITD differences when the spectra at two ears are moderately different.     

Ion mobility spectrometer—field asymmetric ion mobility spectrometer-mass spectrometry

Since the development of electrospray ionization (ESI) for ion mobility spectrometry mass spectrometry (IMMS), IMMS have been extensively applied for characterization of gas-phase bio-molecules. Conventional ion mobility spectrometry (IMS), defined as drift tube IMS (DT-IMS), is typically a stacked ring design that utilizes a low electric field gradient. Field asymmetric ion mobility spectrometry (FAIMS) is a newer version of IMS, however, the geometry of the system is significantly different than DT-IMS and data are collected using a much higher electric field. Here we report construction of a novel ambient pressure dual gate DT-IMS coupled with a FAIMS system and then coupled to a quadrupole ion trap mass spectrometer (QITMS) to form a hybrid three-dimensional separation instrument, DT-IMS-FAIMS-QITMS. The DT-IMS was operated at ~3 Townsend (electric field/number density (E/N) or (Td)) and was coupled in series with a FAIMS, operated at ~80 Td. Ions were mobility-selected by the dual gate DT-IMS into the FAIMS and from the FAIMS the ions were detected by the QITMS for as either MS or MSⁿ. The system was evaluated using cocaine as an analytical standard and tested for the application of separating three isomeric tri-peptides: tyrosine-glycine-tryptophan (YGW), tryptophan-glycine-tyrosine (WGY) and tyrosine-tryptophan-glycine (YWG). All three tri-peptides were separated in the DT-IMS dimension and each had one mobility peak. The samples were partially separated in the FAIMS dimension but two conformation peaks were detected for the YWG sample while YGW and WGY produced only one peak. Ion validation was achieved for all three samples using QITMS.     

Potentiometrie

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