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Abstract. Acacia longifolia, a native legume from Australia, has been introduced in many European countries and elsewhere, thus becoming one of the most important global invasive species. In Europe, its flowering occurs in a period unsuitable for insect activity: nonetheless it is considered entomophilous. Floral traits of this species are puzzling: brightly coloured and scented as liked by insects, but with abundant staminate small-sized flowers and relatively small pollen grains, as it is common in anemophilous species. Invasion processes are especially favoured when reshaping local ecological networks, thus the interest in understanding pollination syndromes associated with invasive plant species that may facilitate invasiveness. Moreover, a striking difference exists between its massive flowering and relatively poor seed set. We introduced a novel approach: first, we consider the possibility that a part of the pollination success is carried on by wind and, second, we weighted the ethological perspective of the main pollinator. During the flowering season of A. longifolia (February-April 2016), we carried on exclusion experiments to detect the relative contribution of insects and wind. While the exclusion experiments corroborated the need for pollen vectors, we actually recorded a low abundance of insects. The honeybee, known pollinator of acacias, was relatively rare and not always productive in terms of successful visits. While wind contributed to seed set, focal observations confirmed that honeybees transfer pollen when visiting both the inflorescences to collect pollen and the extrafloral nectaries to collect nectar. The mixed pollination strategy of A. longifolia may then be the basis of its success in invading Portugal's windy coasts.

Omeprazole (OME) exhibits low stability to light, heat and humidity. In stress conditions OME stability should improve under inclusion complex form with hydroxypropyl-β-cyclodextrin (HPβCD). Stability of OME, its physical mixture (PM) with HPβCD and OME:HPβCD inclusion complex was assessed during 60 days. The inclusion complexes were prepared by kneading and freezedrying techniques and characterized by differential scanning calorimetry (DSC) and Fourier transform infrared spectroscopy (FTIR). A molecular modelling was also held to predict the most probable tridimensional conformation of inclusion complex OME:HPβCD. The inhibitory activity of free and complexed OME on selected enzymes, namely, papain (protease model of the proton pump) and acetylcholinesterase (enzyme present in cholinergic neurons and also involved in Alzheimer's disease) was compared. The results obtained show that HPβCD do not protect against OME degradation, in any prepared powder, in the presence of light, heat and humidity. This may indicate that the reactive group of OME is not included in the HPβCD cavity. This fact is supported by molecular modelling data, which demonstrated that 2-pyridylmethyl group of OME is not included into the cyclodextrin cavity. In relation to enzymatic assays it was observed that free OME and OME in the binary systems showed identical inhibitory activity on papain and acethylcolinesterase, concluding that HPβCD do not affect OME activity on these two enzymes.