User-experience in design and use: enhancing the experience of media content with programmable surround lighting

Table of contents\ud 1 Introduction 4\ud 1.1 Affect and UX 4\ud 1.2 Framework for UX design and evaluation 6\ud 1.3 Programmable surround lighting to enhance UX 6\ud 1.4 UX evaluation 9\ud 1.5 Rationale and research questions 12\ud 2 Method 12\ud 2.1 Design 13\ud 2.2 Participants 13\ud 2.3 Materials and equipment 13\ud 2.4 Procedure 17\ud 3 Results 17\ud 3.1 Aggregated comparisons 18\ud 3.2 Comparisons by clip 27\ud 4 Discussion 29\ud 4.1 The effect of surround lighting on UX 29\ud 4.2 Assimilation effects 33\ud 4.3 Evaluation method 35\ud 4.4 Future work 36\ud 5 Recommendations 38\ud 6 Conclusion 38Programmable surround lighting has the potential to enhance user-experience of media content, but there is a lack of research demonstrating this. Building on existing work in user-experience and Kurosu’s framework for user-experience design and evaluation, we developed a method for testing people’s experience of video content with added programmable controlled surround lighting. We employed simple video content to evoke a response of positive or negative affect. Using a repeated-measures design (N = 33), we manipulated the colour of surround lighting to enhance the affect response (yellow and green for positive affect; red and purple for negative affect) and then tested the benefits of added surround lighting. Yellow surround colour enhanced positive affect in response to video content and red surround colour enhanced negative affect. There was evidence of assimilation effects as a result of alternating coloured (e.g., yellow) and white surround lighting on affect. This work has implications for the choice of surround lighting colour to enhance user-experience, research design and substantive future research.\ud Keywords (up to 6): user-experience evaluation; magnitude-based inference; programmable surround lighting; media content; data analysis; comparative testin

Purinergic Signaling in Kidney Disease

Nucleotides are key subunits for nucleic acids and provide energy for intracellular metabolism. They can also be released from cells to act physiologically as extracellular messengers or pathologically as danger signals. Extracellular nucleotides stimulate membrane receptors in the P2 and P1 family. P2X are ATP- activated cation channels; P2Y and P1 are G-protein coupled receptors activated by ATP, ADP, UTP and UDP or adenosine, respectively. Renal P2 receptors influence both vascular contractility and tubular function. Renal cells also express ectonucleotidases that rapidly hydrolyze extracellular nucleoti des. These enzymes integrate this multi-receptor purinergic-signaling complex by determining the nucleotide milieu, as well as titrating receptor activation. Purinergic signaling also regulates immune cell function by modulating the synthesis and release of various cytokines such as IL1-β and IL-18 as part of inflammasome activation. Abnormal or excessive stimulation of this intricate paracrine system can be pro- or anti-inflammatory, and is also linked to necrosis and apoptosis. Kidney tissue injury causes a localized increase in ATP concentration, and sustained activation of P2 receptors can lead to renal glomerular, tubular and vascular cell damage. Purinergic receptors also regulate the activity and proliferation of fibroblasts, promoting both inflammation and fibrosis in chronic disease. In this short review we summarize some of the recent findings related to purinergic signaling in the kidney. We focus predominantly on the P2X7 receptor, discussing why antagonists have so far disappointed in clinical trials and how advances in our understanding of purinergic signaling might help to reposition these compounds as potential treatments for renal disease

Molecular phylogeny of Subtribe Artemisiinae (Asteraceae), including Artemisia and its allied and segregate genera

BACKGROUND: Subtribe Artemisiinae of Tribe Anthemideae (Asteraceae) is composed of 18 largely Asian genera that include the sagebrushes and mugworts. The subtribe includes the large cosmopolitan, wind-pollinated genus Artemisia, as well as several smaller genera and Seriphidium, that altogether comprise the Artemisia-group. Circumscription and taxonomic boundaries of Artemisia and the placements of these small segregate genera is currently unresolved. RESULTS: We constructed a molecular phylogeny for the subtribe using the internal transcribed spacers (ITS) of nuclear ribosomal DNA analyzed with parsimony, likelihood, and Bayesian criteria. The resulting tree is comprised of three major clades that correspond to the radiate genera (e.g., Arctanthemum and Dendranthema), and two clades of Artemisia species. All three clades have allied and segregate genera embedded within each. CONCLUSIONS: The data support a broad concept of Artemisia s.l. that includes Neopallasia, Crossostephium, Filifolium, Seriphidium, and Sphaeromeria. However, the phylogeny excludes Elachanthemum, Kaschgaria, and Stilnolepis from the Artemisia-group. Additionally, the monophyly of the four subgenera of Artemisia is also not supported, with the exception of subg. Dracunculus. Homogamous, discoid capitula appear to have arisen in parallel four to seven times, with the loss of ray florets. Thus capitular morphology is not a reliable taxonomic character, which traditionally has been one of the defining characters

Molecular phylogeny of Subtribe Artemisiinae (Asteraceae), including \u3ci\u3eArtemisia\u3c/i\u3e and its allied and segregate genera

Background: Subtribe Artemisiinae of Tribe Anthemideae (Asteraceae) is composed of 18 largely Asian genera that include the sagebrushes and mugworts. The subtribe includes the large cosmopolitan, wind-pollinated genus Artemisia, as well as several smaller genera and Seriphidium, that altogether comprise the Artemisia-group. Circumscription and taxonomic boundaries of Artemisia and the placements of these small segregate genera is currently unresolved. Results: We constructed a molecular phylogeny for the subtribe using the internal transcribed spacers (ITS) of nuclear ribosomal DNA analyzed with parsimony, likelihood, and Bayesian criteria. The resulting tree is comprised of three major clades that correspond to the radiate genera (e.g., Arctanthemum and Dendranthema), and two clades of Artemisia species. All three clades have allied and segregate genera embedded within each. Conclusions: The data support a broad concept of Artemisia s.l. that includes Neopallasia, Crossostephium, Filifolium, Seriphidium, and Sphaeromeria. However, the phylogeny excludes Elachanthemum, Kaschgaria, and Stilnolepis from the Artemisia-group. Additionally, the monophyly of the four subgenera of Artemisia is also not supported, with the exception of subg. Dracunculus. Homogamous, discoid capitula appear to have arisen in parallel four to seven times, with the loss of ray florets. Thus capitular morphology is not a reliable taxonomic character, which traditionally has been one of the defining characters

ETA receptor-mediated Ca2+ signaling in thin descending limbs of Henle's loop: Impairment in genetic hypertension

ETA-mediated Ca2+ signaling in thin descending limbs of Henle's loop: Impairment in genetic hypertension.BackgroundEndothelins (ET) have diuretic and natriuretic actions via ETB receptors that are found in most renal tubular segments, although the thin limbs have not been studied. Data also suggest that dysfunction of the renal ET system may be important in the pathogenesis of hypertension. The present study was aimed at determining the presence and nature of ET receptors in the thin limbs of Henle's loop and their ability to activate a Ca2+-dependent signaling pathway, as well as whether ET-induced Ca2+ signals are altered in hypertension.MethodsReverse transcription-polymerase chain reaction (RT-PCR) and Fura 2 fluorescence measurements of [Ca2+]i were made to characterize ET receptors in descending thin limbs (DTL) of Sprague-Dawley rats, spontaneously hypertensive (SH) rats, and control Wistar-Kyoto (WKY) rats, and the three selected strains of Lyon rats with low-normal (LL), normal (LN), and high (LH) blood pressure.ResultsIn SD rats, ET induced Ca2+ signals in DTL of long-looped nephrons, but not in DTL of short loops, or in ascending thin limbs. Ca2+ increases were abolished by BQ123, an antagonist of the ETA receptor, but not by BQ788, an antagonist of the ETB subtype. Endothelin-3 and sarafotoxin 6c, two ETB receptor agonists, were both inactive. RT-PCR showed the presence of both ETA and ETB receptor mRNA. Ca2+ signals measured in DTL of WKY LL and LN rats were similar to those in Sprague-Dawley rats, but were significantly diminished (LH) or abolished (SH) in hypertensive rats.ConclusionA functional ETA receptor activating a Ca2+-dependent pathway is expressed in DTL. This ETA-induced calcium signaling is impaired in two strains of genetically hypertensive rats

First assessment of geophysical sensitivities from spaceborne Galileo and BeiDou GNSS-Reflectometry data collected by the UK TechDemoSat-1 Mission

The UK’s TechDemoSat-1 (TDS-1), launched 2014, has demonstrated the use of global positioning system (GPS) signals for monitoring ocean winds and sea ice. Here it is shown, for the first time, that Galileo and BeiDou signals detected by TDS-1 show similar promise. TDS-1 made seven raw data collections, recovering returns from Galileo and BeiDou, between November 2015 and March 2019. The retrieved open ocean delay Doppler maps (DDMs) are similar to those from GPS. Over sea ice, the Galileo DDMs show a distinctive triple peak. Analysis, adapted from that for GPS DDMs, gives Galileo’s signal-to-noise ratio (SNR), which is found to be inversely sensitive to wind speed, as for GPS. A Galileo track transiting from open ocean to sea ice shows a strong instantaneous SNR response. These results demonstrate the potential of future spaceborne constellations of GNSS-R (global navigation satellite system–reflectometry) instruments for exploiting signals from multiple systems: GPS, Galileo, and BeiDou

Masses of Neutron Stars in High-Mass X-ray Binaries with Optical Astrometry

Determining the type of matter that is inside a neutron star (NS) has been a long-standing goal of astrophysics. Despite this, most of the NS equations of state (EOS) that predict maximum masses in the range 1.4-2.8 solar masses are still viable. Most of the precise NS mass measurements that have been made to date show values close to 1.4 solar masses, but a reliable measurement of an over-massive NS would constrain the EOS possibilities. Here, we investigate how optical astrometry at the microarcsecond level can be used to map out the orbits of High-Mass X-ray Binaries (HMXBs), leading to tight constraints on NS masses. While previous studies by Unwin and co-workers and Tomsick and co-workers discuss the fact that the future Space Interferometry Mission should be capable of making such measurements, the current work describes detailed simulations for 6 HMXB systems, including predicted constraints on all orbital parameters. We find that the direct NS masses can be measured to an accuracy of 2.5% (1-sigma) in the best case (X Per), to 6.5% for Vela X-1, and to 10% for two other HMXBs.Comment: 8 pages, Accepted by Ap

Notice of nodosaur (Dinosauria, Ankylosauria) remains from the mid-Cretaceous of Cambridge, England, with comments on cervical half-ring armour

Three pieces from cervical half-rings of an immature nodosaur, part of a nodosaurid presacral rod and some post-cranial osteoderms from the Cretaceous of Cambridge were studied at the Booth Museum of Natural History, Brighton, UK. Two of the three half-ring elements show dorsal ridge morphologies distinct from each other, and all three have unfused sutured lateral borders. It is possible they may be derived from the same animal. Comparison with other material from the Cretaceous of Europe, USA and Asia indicates the presence of a large nodosaurid in the Cambridge Greensand fauna, with cervical half-ring morphologies similar to North American taxa, but unlike any previously known from the European Cretaceous

Effect of P2X4 and P2X7 receptor antagonism on the pressure diuresis relationship in rats

Reduced glomerular filtration, hypertension and renal microvascular injury are hallmarks of chronic kidney disease, which has a global prevalence of ~10%. We have shown previously shown that the Fischer (F344) rat has lower GFR than the Lewis rat, and is more susceptible to renal injury induced by hypertension. In the early stages this injury is limited to the pre-glomerular vasculature. We hypothesized that poor renal hemodynamic function and vulnerability to vascular injury are causally linked and genetically determined. In the present study, normotensive F344 rats had a blunted pressure diuresis relationship, compared with Lewis rats. A kidney microarray was the interrogated using the Endeavour enrichment tool to rank candidate genes for impaired blood pressure control. Two novel candidate genes, P2rx7 and P2rx4, were identified, having a 7- and 3- fold increased expression in F344 rats. Immunohistochemistry localized P2X4 and P2X7 receptor expression to the endothelium of the pre-glomerular vasculature. Expression of both receptors was also found in the renal tubule; however there was no difference in expression profile between strains. Brilliant Blue G (BBG), a relatively selective P2X7 antagonist suitable for use in vivo, was administered to both rat strains. In Lewis rats, BBG had no effect on blood pressure, but increased renal vascular resistance, consistent with inhibition of some basal vasodilatory tone. In F344 rats BBG caused a significant reduction in blood pressure and a decrease in renal vascular resistance, suggesting that P2X7 receptor activation may enhance vasoconstrictor tone in this rat strain. BBG also caused reduced the pressure diuresis threshold in F344 rats, but did not alter its slope. These preliminary findings suggest a physiological and potential pathophysiological role for P2X7 in controlling renal and/or systemic vascular function, which could in turn affect susceptibility to hypertension-related kidney damage