Abstract The present study was based on the analysis of 10,467 trawls of the industrial piramutaba (Brachyplatystoma vaillantii) fishing fleet of the Brazilian state of Pará, which were mapped by onboard GPS loggers (between February 2008 and September 2011) and the PREPS data from 40 vessels which were tracked by this system between 2008 and 2011. The variation in the mean monthly CPUE, based on Lomb’s periodogram, revealed a well-defined and constant cycle with a duration of approximately one year. Three environmental factors influenced this cycle. The El Niño 3.4 index had a negative correlation with the CPUE of the piramutaba fishery, with a time lag of 15 months, while monthly rainfall and the mean discharge of the Amazon River correlated strongly (r=0.89 and 0.87, respectively; p<0.001) with the CPUE, with time lags of 12 and 11 months, respectively. The spatiotemporal analysis of the distribution of the activity of the piramutaba fishing fleet indicated that the most intense area of operation of the fleet lies between latitudes 00º N and 02° N, and longitudes 047º40’ W and 049º40’ W. This area was divided into four geographic quadrants, although fishery operations were concentrated in only three of these quadrants. The study proposed a quadrimester fishing cycle with zoning in three of the quadrants, where fishing would be permitted for four months (occupation period), followed by an 8-month rest period for the recuperation of stocks, aiming at the sustainability of this fishing exploration.

Drug trafficking and the introduction of new drugs onto the illicit market are one of the main challenges of the forensic community. In this study, the chemical profile of a new designer drug, 2-(4-iodine-2,5-dimethoxyphenyl)-n-[(2-methoxyphenyl)methyl]etamine or 25I-NBOMe was explored using thin layer chromatography (TLC), ultraviolet-visible spectrophotometry (UV-Vis), attenuated total reflection with Fourier transform infrared spectroscopy(ATR-FTIR), gas chromatography mass spectrometry (GC-MS) and electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry (ESI-FT-ICR MS). First, the TLC technique was effective for identifying spots related to 25C-, 25B- and 25I-NBOMe compounds, all with the same retention factor, Rf ≈ 0.50. No spot was detected for 2,5-dimethoxy-4-bromoamphetamine, 2,5-Dimethoxy-4-chloroamphetamine or lysergic acid diethylamide compounds. ATR-FTIR preserved the physical-chemical properties of the material, whereas GC-MS and ESI-MS showed better analytical selectivity. ESI(+)FT-ICR MS was used to identify the exact mass (m/z428.1706 for the [M + H]+ ion), molecular formula (M = C18H22INO3), degree of unsaturation (DBE = 8) and the chemical structure (from collision induced dissociation, CID, experiments) of the 25I-NBOMe compound. Furthermore, the ATR-FTIR and CID results suggested the presence of isomers, where a second structure is proposed as an isomer of the 25I-NBOMe molecule.