The determinants of length of stay in the Azores : a count model approach

This paper employs count data models to estimate the determinants of length of stay, as count data models naturally lend themselves to overcome the censoring and truncation data issues associated with the non-negative, integer nature of length of stay. This paper employs a rich micro data set gathered through questionnaires ministered to a representative sample of tourists departing from the Azores: the fastest growing touristic region in Portugal. It is found that sociodemographic profiles, such as nationality and Azorean ascendancy, and trip attributes, such as repeat visitation rates and type of flight, are important determinants of length of stay. In addition, it is found that destination image and attitudes regarding environmental initiatives, constructed from a factor analysis exercise, also influence length of stay. In particular, the results suggest that marketing strategies that promote the Azores for its nature, landscape, remoteness, weather and safety may increase length of stay, whereas cultural heritage has the opposite effect.N/

Policy Coordination in an Oligopolistic Housing Market

This paper analyzes the consequences of the interaction between two different levels of government (regulators) in the development of housing policy when their decisions determine the level of competition in the housing market. The analysis discusses the implications derived from a lack of coordination between a local regulator who controls the supply of land for housing development and a central regulator who decides on housing subsidies. The results suggest that lack of coordination has significant effects on prices and supply of houses, housing developers’ profits, and buyers’ surplus.imperfect competition, housing policy coordination

Unravelling the surface chemistry of metal oxide nanocrystals, the role of acids and bases

We synthesized HfO2 nanocrystals from HfCl4 using a surfactant-free solvothermal process in benzyl alcohol and found that the resulting nanocrystals could be transferred to nonpolar media using a mixture of carboxylic acids and amines. Using solution 1H NMR, FTIR, and elemental analysis, we studied the details of the transfer reaction and the surface chemistry of the resulting sterically stabilized nanocrystals. As-synthesized nanocrystals are charge-stabilized by protons, with chloride acting as the counterion. Treatment with only carboxylic acids does not lead to any binding of ligands to the HfO2 surface. On the other hand, we find that the addition of amines provides the basic environment in which carboxylic acids can dissociate and replace chloride. This results in stable, aggregate-free dispersions of HfO2 nanocrystals, sterically stabilized by carboxylate ligands. Moreover, titrations with deuterated carboxylic acid show that the charge on the carboxylate ligands is balanced by coadsorbed protons. Hence, opposite from the X-type/nonstoichiometric nanocrystals picture prevailing in literature, one should look at HfO2/carboxylate nanocrystals as systems where carboxylic acids are dissociatively adsorbed to bind to the nanocrystals. Similar results were obtained with ZrO2 NCs. Since proton accommodation on the surface is most likely due to the high Brønsted basicity of oxygen, our model could be a more general picture for the surface chemistry of metal oxide nanocrystals with important consequences on the chemistry of ligand exchange reactions

Assessing User Expertise in Spoken Dialog System Interactions

Identifying the level of expertise of its users is important for a system since it can lead to a better interaction through adaptation techniques. Furthermore, this information can be used in offline processes of root cause analysis. However, not much effort has been put into automatically identifying the level of expertise of an user, especially in dialog-based interactions. In this paper we present an approach based on a specific set of task related features. Based on the distribution of the features among the two classes - Novice and Expert - we used Random Forests as a classification approach. Furthermore, we used a Support Vector Machine classifier, in order to perform a result comparison. By applying these approaches on data from a real system, Let's Go, we obtained preliminary results that we consider positive, given the difficulty of the task and the lack of competing approaches for comparison.Comment: 10 page

Two distinct arabinofuranosidases contribute to arabino-oligosaccharide degradation in Bacillus subtilis.

Microbiology 154 (2008) 2719-2729Bacillus subtilis produces alpha-l-arabinofuranosidases (EC 3.2.1.55; AFs) capable of releasing arabinosyl oligomers and l-arabinose from plant cell walls. Here, we show by insertion-deletion mutational analysis that genes abfA and xsa(asd), herein renamed abf2, encode AFs responsible for the majority of the intracellular AF activity in B. subtilis. Both enzyme activities were shown to be cytosolic and functional studies indicated that arabino-oligomers are natural substrates for the AFs. The products of the two genes were overproduced in Escherichia coli, purified and characterized. The molecular mass of the purified AbfA and Abf2 was about 58 kDa and 57 kDa, respectively. However, native PAGE gradient gel analysis and cross-linking assays detected higher-order structures (>250 kDa), suggesting a multimeric organization of both enzymes. Kinetic experiments at 37 degrees C, with p-nitrophenyl-alpha-l-arabinofuranoside as substrate, gave an apparent K(m) of 0.498 mM and 0.421 mM, and V(max) of 317 U mg(-1) and 311 U mg(-1) for AbfA and Abf2, respectively. The two enzymes displayed maximum activity at 50 degrees C and 60 degrees C, respectively, and both proteins were most active at pH 8.0. AbfA and Abf2 both belong to family 51 of the glycoside hydrolases but have different substrate specificity. AbfA acts preferentially on (1-->5) linkages of linear alpha-1,5-l-arabinan and alpha-1,5-linked arabino-oligomers, and is much less effective on branched sugar beet arabinan and arabinoxylan and arabinogalactan. In contrast, Abf2 is most active on (1-->2) and (1-->3) linkages of branched arabinan and arabinoxylan, suggesting a concerted contribution of these enzymes to optimal utilization of arabinose-containing polysaccharides by B. subtilis.This work was partially supported by grant no. POCI/AGR/60236/2004 from the Fundacao para a Ciencia e Tecnologia (FCT) and FEDER to I. d. S.- N., and fellowship SFRH/BD/18238/2004 from the FCT to J. M. I

Use of a new enrichment nanosorbent for speciation of mercury by FI-CV-ICP-MS

Mercury is one of the most toxic environmental pollutants and its effects on human and ecosystem health are well known. All mercury species are toxic, with organic mercury compounds generally being more toxic than inorganic species. Chromatography techniques (GC, HPLC) coupled to element specific detectors, are able to separate mercury species in order to elucidate mercury transformation and transport processes where the determination of all mercury species is desirable. However, in practice, especially in sampling campaigns for sea water analysis where a large number of samples are collected over a longer period of time, a combination of methods is usually applied to accurately determine the most toxic mercury species. These include non-chromatographic methods based on the different chemical and/or physical behavior of the mercury species. These non-chromatographic methods can be less time consuming, more cost effective and available, and present competitive limits of detection. Especially when mercury could vapor (CV) generation technique is employed, which reduces salt effect on the analytical signal and improve the sensibility. Among non-chromatographic methods, solid phase extraction and microextraction (SPE and SPME) which is becoming increasingly popular for sample preparation in organic analysis, found its way to speciation analysis of organometals. SPE/SPME is the most popular sample preconcentration method for its simplicity, high enrichment factor, low or no consumption of organic solvents and feasibly to be automated. On the other hand, the exploration of new materials, especially nanometer sized materials, as the support phase is another active research area in SPE/SPME for mercury determination. The use of nanoparticles leads to higher extraction capacity/efficiency and rapid dynamics of extraction originated from the higher surface area to volume ratio and short diffusion route. In this work, a new enrichment nanosorbent functionalized with 1,5 bis (2-pyridyl) methylene thiocarbohidrazide was synthesized and characterized. From the study of its adsorption capacity toward metal ions, Hg2+ was observed to be one of the most retained 173.1 µmol g-1 at pH 5. Thus, a flow injection solid phase extraction and cold vapor generation method for its determination and speciation based on the use of this new chelating nanosorbent was optimized. The method developed has showed to be useful for the automatic pre-concentration and sequential speciation of mercury and methylmercury in environmental and biological samples. The system was based on chelating retention of the analytes onto a mini-column filled with the new nanosorbent and their sequential elution by using two different eluents, 0.2 % HCl for CH3Hg+ and 0.1 % thiourea in 0.5 % HCl for Hg2+. The determination was performed using inductively coupled plasma mass spectrometry. Under the optimum conditions and 120 s preconcentration time, the enrichment factors were 4.7 and 11.0; the detection limits (3σ) were 0.002 and 0.004 µg L-1; the determination limits (10σ) were 0.011 and 0.024 µg L-1; and the precisions (calculated for 10 replicate determinations at a 2 µg L-1 standard of both species) were 2.8 and 2.6 % (RSD); for CH3Hg+ and Hg2+, respectively. Linear calibration graphs were obtained for both species from the determination limits to at least 70 µg L-1. For the quality control of the analytical performance and the validation of the newly developed method, the analysis of two certified samples, LGC 6016 estuarine water and SRM 2976 mussel tissue were addressed. The results showed good agreement with the certified values. The method was successfully applied to the speciation of mercury in sea-water samples collected in the Málaga Bay.Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tech

Towards a comparable evaluation for VANET protocols: NS-2 experiments builder assistant and extensible test bed

Proceedings of: 9th Embedded Security in Cars Conference (ESCAR 2011), November 9 to 10, 2011, Dresden, GermanyIn order to validate an Intelligent Transportation System (ITS) application or service, simulation techniques are usually employed. Nowadays, there are two problems associated to this kind of validation: the relative complexity of existing simulators and the lack of common criteria in the creation of simulation experiments. The first one makes it hard for users not familiar with a simulation tool to create and execute comprehensive experiments. The second one leads to a situation in which different proposals are validated in different scenarios, thus making it difficult to compare their performance. This work contributes on addressing both problems by proposing VanSimFM, an open-source assistant tool for creating NS-2 simulation experiments, and by defining an extensible test bed which contains a set of simulation scenarios. The test bed is intended to represent the different situations that may be found in a real vehicular environment.This work is partially supported by Ministerio de Ciencia e Innovacion of Spain, project E-SAVE, under grant TIN2009-13461.No publicad

Aqueous ZrO 2 and YSZ colloidal systems through microwave assisted hydrothermal synthesis

In this paper, the formation of ZrO2 and yttria-stabilised-zirconia (YSZ) aqueous colloidal systems via microwave assisted hydrothermal synthesis is studied. Microwave synthesis allows a fast screening of the influence of different parameters such as time and temperature. The temperature varied from 140 degrees C up to 180 degrees C and the used reaction time varied from 5 min up to 1 h. The synthesised zirconia nanoparticles have a particle size of 50 nm confirmed by TEM. A H-1 NMR (nuclear magnetic resonance) study helped to understand the stabilization mechanism of the synthesised particles. By the addition of ytrrium ions into the zirconia colloidal solution, YSZ could be formed via an additional thermal treatment. Hereby, the samples are heated up to 400 degrees C for 1 h. YSZ colloidal solutions are synthesised by making use of complexing agents such as nitrilotriacetic acid, ethylenediaminetetraacetic acid and citric acid to control the hydrolysis and condensation of both ions to avoid non-stoichiometric phases. The ratio of Zr/Y in the particles is quantified by XRF. The amorphous structure of those particles necessitates an additional thermal treatment up to 600 degrees C during 1 h in order to obtain crystalline YSZ

Synthesis and characterization of a new nanosorbent based on functionalized magnetic nanoparticles and its use in the determination of mercury by FI-CV-ETAAS

In this work, a new chelating sorbent which employs 1,5-bis(di-2-pyridil)methylene thiocarbohydrazide as the functional group and magnetic nanoparticles (MNPs) as its support (DPTH-MNP) was synthetized and characterized. The MNPs were prepared by coprecipitation of Fe+2 and Fe+3 with NH3 and then coated with silica in order to easily bind the support and the functionalizing molecule. The aim of the synthesis of this material is applying it as a solid-phase extracting agent and evaluating its potential for the extraction and pre-concentration of trace amounts of analytes present in biological and environmental samples with on-line methods. The MNPs’ magnetic core would allow overcoming the usual backpressure problems that happen in solid-phase extraction methods thanks to the possibility of immobilizing the MNPs by applying an external magnetic field. From the study of its adsorption capacity toward metal ions, mercury and antimony were the most retained. Thus, a flow injection solid phase extraction and cold vapor generation method for mercury determination based on the use of this new chelating nanosorbent was optimized. The greatest efforts were put into the reactor design to minimize compaction and loss of nanosorbent. The knotted reactor shown in Figure 1 was chosen as the best. Then, chemical and flow variables were optimized by Central composite designs (CCDs). The method developed has showed to be useful for the automatic pre-concentration and determination of mercury in environmental and biological samples. The determination was performed using electrothermal atomic absorption spectrometry (ETAAS). Under the optimum conditions, pH 5 and 120 s preconcentration time, the enrichment factor was 5.33; the detection limit (3σ) was 7.8 ng L-1; the determination limit (10σ) was 99 ng L-1; and the precisions (calculated for 10 replicate determinations at a 1 and 5 µg L-1 standards) were 1.7 and 1.9 % (RSD), respectively. Two linear calibration graphs were obtained, from the determination limits to 10 µg L-1 and from 10 to at least 50 µg L-1. From the comparison with other similar methods found in the bibliography, the detection limit and precisions calculated with our method were better. In order to evaluate the accurate and applicability of the method, the analysis of five certified samples LGC 6016 estuarine water, TMDA 54.4 fortified lake water, SRM 2976 mussel tissue, TORT-1 lobster hepatopancreas and DOLT-1 dogfish liver by standard addition and external calibration, were addressed. The results showed good agreement between the certified values, or added amounts of mercury, and the found concentrations. The method was successfully applied to the determination of mercury in sea-water samples collected in the Málaga Bay.Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tec