Creation of digital tools for a better foreign visitor experience of Espai Far

Treball desenvolupat dins el marc del programa 'European Project Semester'.This document will explore a research which have been done for a museum located in Vilanova I La Getru, Catalonia, Spain. The museum is called Espai Far, what stands for Lighthouse space. Espai Far approached UPC to find a team of international students for doing research and for identifying the approaches the museum needs, to increase the users experience. The team is a group of international designers and engineers on an international design semester, each possessing skills and attributes which will be essential for the completion of this project. Espai Far shows the richness of Vilanova’s maritime inheritance. The Espai Far has three exhibition spaces and opened in July, 2016. The project began at the beginning of February 2017. The team fist got introduced with the museum itself. The first thing which got clear was that al the information was only available in Catalan, besides that the museum has limited space which leaves no room for translation in other languages. The main goal for this project is to improve the visitors’ experience. Firstly, the team wanted to know who are the visitors of Espai Far? Therefore, the team decided to do research on the visitors’ experience, the number of visitors and their origins. With the answers which are provided from this surveys, it became clear for the team which further steps have to be taken. In collaboration with the supervisors there has be agreed on the next steps: • Create new digital tools o Webpage For the most effective template the team did research which can be found in chapter seven. This chapter shows some examples and mock-ups about the final website. Unfortunate the team was not able to create a working webpage and the webpage is now still under construction. o Promotion video´s The team made as well a promotion video with several pictures about Espai Far. In the video shows about the three different parts of the museum, the collaboration with schools and about other activities they organise. The video can be used on the webpage of Espai Far or for instance on social media. Besides the webpage and the promotion videos the team decided to create four more digital tools. First, the team created a navigation video, which shows the route from the train station in Vilanova to Espai Far. In the video shows pictures, street names and recognition sites. Second, panoramic pictures of the museum. Third, the use of QR-codes. Fourth, surveys on GoogleDocs. • Translate the most important information about the museum, which can be placed on the new webpage: The most important information is translated in multiple languages Spanish, English, French and Dutch. • Research on marketing purpose: To discover how Espai far can improve the visitors experience as well, the team did research on the marketing approach of Espai Far. The team had an interview with Mar Sanchez, the director of Espai Far about the actual situation of Espai Far. Besides that, the team also took interviews with other museums as well to compare their strategies with Espai Far’s. • Improve the interactivity in the museum: Interactivity in the museum is also a part of the user experience, that´s why the team invented some interactive ideas for Espai Far. These ideas can be found in chapter 6.2

A conceptual map of invasion biology: Integrating hypotheses into a consensus network

Background and aims Since its emergence in the mid‐20th century, invasion biology has matured into a productive research field addressing questions of fundamental and applied importance. Not only has the number of empirical studies increased through time, but also has the number of competing, overlapping and, in some cases, contradictory hypotheses about biological invasions. To make these contradictions and redundancies explicit, and to gain insight into the field’s current theoretical structure, we developed and applied a Delphi approach to create a consensus network of 39 existing invasion hypotheses. Results The resulting network was analysed with a link‐clustering algorithm that revealed five concept clusters (resource availability, biotic interaction, propagule, trait and Darwin’s clusters) representing complementary areas in the theory of invasion biology. The network also displays hypotheses that link two or more clusters, called connecting hypotheses, which are important in determining network structure. The network indicates hypotheses that are logically linked either positively (77 connections of support) or negatively (that is, they contradict each other; 6 connections). Significance The network visually synthesizes how invasion biology’s predominant hypotheses are conceptually related to each other, and thus, reveals an emergent structure – a conceptual map – that can serve as a navigation tool for scholars, practitioners and students, both inside and outside of the field of invasion biology, and guide the development of a more coherent foundation of theory. Additionally, the outlined approach can be more widely applied to create a conceptual map for the larger fields of ecology and biogeography

DNAzymes as Catalysts for l-Tyrosine and Amyloid β Oxidation

Single-stranded deoxyribonucleic acids have an enormous potential for catalysis by applying tailored sequences of nucleotides for individual reaction conditions and substrates. If such a sequence is guanine-rich, it may arrange into a three-dimensional structure called G-quadruplex and give rise to a catalytically active DNA molecule, a DNAzyme, upon addition of hemin. Here, we present a DNAzyme-mediated reaction, which is the oxidation of l-tyrosine toward dityrosine by hydrogen peroxide. With an optimal stoichiometry between DNA and hemin of 1:10, we report an activity of 101.2 ± 3.5 μUnits (μU) of the artificial DNAzyme Dz-00 compared to 33.0 ± 1.8 μU of free hemin. Exemplarily, DNAzymes may take part in neurodegeneration caused by amyloid beta (Aβ) aggregation due to l-tyrosine oxidation. We show that the natural, human genome-derived DNAzyme In1-sp is able to oxidize Aβ peptides with a 4.6% higher yield and a 33.3% higher velocity of the reaction compared to free hemin. As the artificial DNAzyme Dz-00 is even able to catalyze Aβ peptide oxidation with a 64.2% higher yield and 337.1% higher velocity, an in-depth screening of human genome-derived DNAzymes may identify further candidates with similarly high catalytic activity in Aβ peptide oxidation

Spinel-structured ZnCr2O4 with excess Zn is the active ZnO/Cr2O3 catalyst for high-temperature methanol synthesis

A series of ZnO/Cr2O3 catalysts with different Zn:Cr ratios was prepared by coprecipitation at a constant pH of 7 and applied in methanol synthesis at 260–300 °C and 60 bar. The X-ray diffraction (XRD) results showed that the calcined catalysts with ratios from 65:35 to 55:45 consist of ZnCr2O4 spinel with a low degree of crystallinity. For catalysts with Zn:Cr ratios smaller than 1, the formation of chromates was observed in agreement with temperature-programmed reduction results. Raman and XRD results did not provide evidence for the presence of segregated ZnO, indicating the existence of Zn-rich nonstoichiometric Zn–Cr spinel in the calcined catalyst. The catalyst with Zn:Cr = 65:35 exhibits the best performance in methanol synthesis. The Zn:Cr ratio of this catalyst corresponds to that of the Zn4Cr2(OH)12CO3 precursor with hydrotalcite-like structure obtained by coprecipitation, which is converted during calcination into a nonstoichiometric Zn–Cr spinel with an optimum amount of oxygen vacancies resulting in high activity in methanol synthesis. Density functional theory calculations are used to examine the formation of oxygen vacancies and to measure the reducibility of the methanol synthesis catalysts. Doping Cr into bulk and the (10–10) surface of ZnO does not enhance the reducibility of ZnO, confirming that Cr:ZnO cannot be the active phase. The (100) surface of the ZnCr2O4 spinel has a favorable oxygen vacancy formation energy of 1.58 eV. Doping this surface with excess Zn charge-balanced by oxygen vacancies to give a 60% Zn content yields a catalyst composed of an amorphous ZnO layer supported on the spinel with high reducibility, confirming this as the active phase for the methanol synthesis catalyst

Ionization balance of Ti in the photospheres of the Sun and four late-type stars

In this paper we investigate statistical equilibrium of Ti in the atmospheres of late-type stars. The Ti I/Ti II level populations are computed with available experimental atomic data, except for photoionization and collision induced transition rates, for which we have to rely on theoretical approximations. For the Sun, the NLTE line formation with adjusted H I inelastic collision rates and MAFAGS-OS model atmosphere solve the long-standing discrepancy between Ti I and Ti II lines. The NLTE abundances determined from both ionization stages agree within $0.01$ dex with each other and with the Ti abundance in C I meteorites. The Ti NLTE model does not perform similarly well for the metal-poor stars, overestimating NLTE effects in the atmospheres of dwarfs, but underestimating overionization for giants. Investigating different sources of errors, we find that only [Ti/Fe] ratios based on Ti II and Fe II lines can be safely used in studies of Galactic chemical evolution. To avoid spurious abundance trends with metallicity and dwarf/giant discrepancies, it is strongly recommended to disregard Ti I lines in abundance analyses, as well as in determination of surface gravities.Comment: 16 pages, accepted for publication in MNRA

Predicting functional gains in a stroke trial.

A number of therapies in development for patients with central nervous system injury aim to reduce disability by improving function of surviving brain elements rather than by salvaging tissue. The current study tested the hypothesis that, after adjusting for a number of clinical assessments, a measure of brain function at baseline would improve prediction of behavioral gains after treatment.Twenty-four patients with chronic stroke underwent baseline clinical and functional MRI assessments, received 6 weeks of rehabilitation therapy with or without investigational motor cortex stimulation, and then had repeat assessments. Thirteen baseline clinical/radiological measures were evaluated for ability to predict subsequent trial-related gains.Across all patients, bivariate analyses found that greater trial-related functional gains were predicted by (1) smaller infarct volume, (2) greater baseline clinical status, and (3) lower degree of activation in stroke-affected motor cortex on baseline functional MRI. When these 3 variables were further assessed using multivariate linear regression modeling, only lower motor cortex activation and greater clinical status at baseline remained significant predictors. Note that lower baseline motor cortex activation was also associated with larger increases in motor cortex activation after treatment.Lower motor cortex activity at baseline predicted greater behavioral gains after therapy, even after controlling for a number of clinical assessments. The boosts in cortical activity that paralleled behavioral gains suggest that in some patients, low baseline cortical activity represents underuse of surviving cortical resources. A measure of brain function might be important for optimal clinical decision-making in the context of a restorative intervention

Negative feedback regulation of MAPK signaling is an important driver of chronic lymphocytic leukemia progression

Despite available targeted treatments for the disease, drug-resistant chronic lymphocytic leukemia (CLL) poses a clinical challenge. The objective of this study is to examine whether the dual-specific phosphatases DUSP1 and DUSP6 are required to negatively regulate mitogen-activated protein kinases (MAPKs) and thus counterbalance excessive MAPK activity. We show that high expression of DUSP6 in CLL correlates with poor clinical prognosis. Importantly, genetic deletion of the inhibitory phosphatase DUSP1 or DUSP6 and blocking DUSP1/6 function using a small-molecule inhibitor reduces CLL cell survival in vitro and in vivo. Using global phospho-proteome approaches, we observe acute activation of MAPK signaling by DUSP1/6 inhibition. This promotes accumulation of mitochondrial reactive oxygen species and, thereby, DNA damage and apoptotic cell death in CLL cells. Finally, we observe that DUSP1/6 inhibition is particularly effective against treatment-resistant CLL and therefore suggest transient DUSP1/6 inhibition as a promising treatment concept to eliminate drug-resistant CLL cells