The peculiar attraction of royalty for tourism and the popular cultural construction of ‘Royal Tourism’

In 2008, we explored both implicit and explicit relationships between royalty and tourism in contemporary and historic UK and some international contexts. In doing so, we provided an original, direct and specific focus on the hitherto neglected subject of ‘Royal Tourism’ (Long and Palmer, 2008). A range of historical, sociological and popular cultural perspectives were included as a basis for examining the royal tourism phenomenon. There has to date, and surprisingly given the continuing relevance of the subject and enduring prominence of royalty, been no further academic studies of which we are aware that focus specifically on this royal tourism phenomenon. Nine years on, we revisit the peculiar attraction of royalty for tourism and specifically consider an enduring and persistent touristic focus on the monarchy, particularly in the UK. This chapter re-investigates the concept of 'Royal Tourism' as a specific form of popular cultural tourism and considers how royal tourism may be employed not solely for economic gain and commercial exploitation (one of the most enduring and publically contested aspects of the relationships between tourism and monarchy) but also as a political and socio-cultural tool and context. We consider Royal Tourism as a socially constructed concept (Berger and Luckman, 1966), whereby the entering into and playing out of roles and reciprocal actions by members of society as tourists are institutionalized. Thus, responses to royalty, in a tourism context, are embedded in the institutional fabric of society and popular culture. To explore this, we draw on our 2008 book though this material is adapted and updated to focus on popular cultural dimensions of Royal Tourism. The chapter considers, in turn: how there persists a focus on monarchy per se and in specific relation to royal events and tourism development and marketing activities; royal families and their prominent contribution to the reproduction of social mores and the establishment of tourist destinations through their patronage; the politics of Royal Tourism; and Royal Tourism’s meeting of psychological and physiological needs for the tourist. It then attempts to make sense of these features collectively to consider how understanding of this specific form of tourism can inform and assist deeper understanding of tourism within a wider popular cultural context

Overturn of ilmenite‐bearing cumulates in a rheologically weak lunar mantle

©2019. American Geophysical UnionThe crystallization of the lunar magma ocean (LMO) determines the initial structure of the solid Moon. Near the end of the LMO crystallization, ilmenite‐bearing cumulates (IBC) form beneath the plagioclase crust. Being denser than the underlying mantle, IBC are prone to overturn, a hypothesis that explains several aspects of the Moon's evolution. Yet the formation of stagnant lid due to the temperature dependence of viscosity can easily prevent IBC from sinking. To infer the rheological conditions allowing IBC to sink, we calculated the LMO crystallization sequence and performed high‐resolution numerical simulations of the overturn dynamics. We assumed a diffusion creep rheology and tested the effects of reference viscosity, activation energy, and compositional viscosity contrast between IBC and mantle. The overturn strongly depends on reference viscosity and activation energy and is facilitated by a low IBC viscosity. For a reference viscosity of 1021 Pa s, characteristic of a dry rheology, IBC overturn cannot take place. For a reference viscosity of 1020 Pa s, the overturn is possible if the activation energy is a factor of 2–3 lower than the values typically assumed for dry olivine. These low activation energies suggest a role for dislocation creep. For lower‐reference viscosities associated with the presence of water or trapped melt, more than 95% IBC can sink regardless of the activation energy. Scaling laws for Rayleigh‐Taylor instability confirmed these results but also showed the need of numerical simulations to accurately quantify the overturn dynamics. Whenever IBC sink, the overturn occurs via small‐scale diapirs

Generating High-Resolution 3D Faces and Bodies Using VQ-VAE-2 with PixelSNAIL Networks on 2D Representations

Modeling and representing 3D shapes of the human body and face is a prominent field due to its applications in the healthcare, clothes, and movie industry. In our work, we tackled the problem of 3D face and body synthesis by reducing 3D meshes to 2D image representations. We show that the face can naturally be modeled on a 2D grid. At the same time, for more challenging 3D body geometries, we proposed a novel non-bijective 3D–2D conversion method representing the 3D body mesh as a plurality of rendered projections on the 2D grid. Then, we trained a state-of-the-art vector-quantized variational autoencoder (VQ-VAE-2) to learn a latent representation of 2D images and fit a PixelSNAIL autoregressive model to sample novel synthetic meshes. We evaluated our method versus a classical one based on principal component analysis (PCA) by sampling from the empirical cumulative distribution of the PCA scores. We used the empirical distributions of two commonly used metrics, specificity and diversity, to quantitatively demonstrate that the synthetic faces generated with our method are statistically closer to real faces when compared with the PCA ones. Our experiment on the 3D body geometry requires further research to match the test set statistics but shows promising results

Targeted disruption of the Kcnj5 gene in the female mouse lowers aldosterone levels.

Aldosterone is released from adrenal zona glomerulosa (ZG) cells and plays an important role in Na and K homoeostasis. Mutations in the human inwardly rectifying K channel CNJ type (KCNJ) 5 (KCNJ5) gene encoding the G-coupled inwardly rectifying K channel 4 (GIRK4) cause abnormal aldosterone secretion and hypertension. To better understand the role of wild-type (WT) GIRK4 in regulating aldosterone release, we have looked at aldosterone secretion in a Kcnj5 knockout (KO) mouse. We found that female but not male KO mice have reduced aldosterone levels compared with WT female controls, but higher levels of aldosterone after angiotensin II (Ang-II) stimulation. These differences could not be explained by sex differences in aldosterone synthase (Cyp11B2) gene expression in the mouse adrenal. Using RNAseq analysis to compare WT and KO adrenals, we showed that females also have a much larger set of differentially expressed adrenal genes than males (395 compared with 7). Ingenuity Pathway Analysis (IPA) of this gene set suggested that peroxisome proliferator activated receptor (PPAR) nuclear receptors regulated aldosterone production and altered signalling in the female KO mouse, which could explain the reduced aldosterone secretion. We tested this hypothesis in H295R adrenal cells and showed that the selective PPARα agonist fenofibrate can stimulate aldosterone production and induce Cyp11b2. Dosing mice in vivo produced similar results. Together our data show that Kcnj5 is important for baseline aldosterone secretion, but its importance is sex-limited at least in the mouse. It also highlights a novel regulatory pathway for aldosterone secretion through PPARα that may have translational potential in human hyperaldosteronism

Technical solutions to improve global sustainable management of waste electrical and electronic equipment (WEEE) in the EU and China

With the amount of Waste Electrical and Electronic Equipment (WEEE) being generated every year and increasing at an accelerating rate, the management of electronic waste (e-waste) has become an important global issue. This article contains a literature survey and a practical study of five mobile phones. In the literature survey WEEE management approaches in the EU and China were evaluated to identify differences and commonalities in approach as well as the identification of the current best practices. Practical End-of-Life (EoL) treatment processes, including remanufacturing, reconditioning, repairing, recycling, repurposing, reusing and disposal of e-waste were all investigated and studied in context of mobile phones. In the phone disassembly exercise the component material, weight, joining method, possibility of re-attachment and damage of disassembly were identified and noted down for every removed component. This disassembly gave insight in how the WEEE management in the EU could be adapted to improve the amount of component recovery. A final suggestion is to implement an EU objective open-access component database where original equipment manufacturer (OEM) component data and updated component performance information can be found. This would improve the quality and identification of components and hence aid component recovery

Embedding alkenes within an icosahedral inorganic fullerene {(NH4)42[Mo132O372(L)30(H2O)72]} for trapping volatile organics

Eight alkene-functionalized molybdenum-based spherical Keplerate-type (inorganic fullerene) structures have been obtained via both direct and multistep synthetic approaches. Driven by the opportunity to design unique host–guest interactions within hydrophobic, π-electron rich confined environments, we have synthesised {(NH4)42[Mo132O372(L)30(H2O)72]}, where L = (1) acrylic acid, (2) crotonic acid, (3) methacrylic acid, (4) tiglic acid, (5) 3-butenoic acid, (6) 4-pentenoic acid, (7) 5-hexenoic acid, and (8) sorbic acid. The compounds, which are obtained in good yield (10–40%), contain 30 carboxylate-coordinated alkene ligands which create a central cavity with hydrophobic character. Extensive Nuclear Magnetic Resonance (NMR) spectroscopy studies contribute significantly to the complete characterisation of the structures obtained, including both 1D and 2D measurements. In addition, single-crystal X-ray crystallography and subsequently-generated electron density maps are employed to highlight the distribution in ligand tail positions. These alkene-containing structures are shown to effectively encapsulate small alkyl thiols (1-propanethiol (A), 2-propanethiol (B), 1-butanethiol (C), 2-butanethiol (D) and 2-methyl-1-propanethiol (E)) as guests within the central cavity in aqueous solution. The hydrophobically driven clustering of up to 6 equivalents of volatile thiol guests within the central cavity of the Keplerate-type structure results in effective thermal protection, preventing evaporation at elevated temperatures (ΔT ≈ 25 K)

A modular programmable inorganic cluster discovery robot for the discovery and synthesis of polyoxometalates

The exploration of complex multicomponent chemical reactions leading to new clusters, where discovery requires both molecular self-assembly and crystallization, is a major challenge. This is because the systematic approach required for an experimental search is limited when the number of parameters in a chemical space becomes too large, restricting both exploration and reproducibility. Herein, we present a synthetic strategy to systematically search a very large set of potential reactions, using an inexpensive, high-throughput platform that is modular in terms of both hardware and software and is capable of running multiple reactions with in-line analysis, for the automation of inorganic and materials chemistry. The platform has been used to explore several inorganic chemical spaces to discover new and reproduce known tungsten-based, mixed transition-metal polyoxometalate clusters, giving a digital code that allows the easy repeat synthesis of the clusters. Among the many species identified in this work, the most significant is the discovery of a novel, purely inorganic W24FeIII–superoxide cluster formed under ambient conditions. The modular wheel platform was employed to undertake two chemical space explorations, producing compounds 1–4: (C2H8N)10Na2[H6Fe(O2)W24O82] (1, {W24Fe}), (C2H8N)72Na16[H16Co8W200O660(H2O)40] (2, {W200Co8}), (C2H8N)72Na16[H16Ni8W200O660(H2O)40] (3, {W200Ni8}), and (C2H8N)14[H26W34V4O130] (4, {W34V4}), along with many other known species, such as simple Keggin clusters and 1D {W11M2+} chains

Studying Kaon-pion S-wave scattering in K-matrix formalism

We generalize our previous work on \pi\pi scattering to K\pi scattering, and re-analyze the experiment data of K\pi scattering below 1.6 GeV. Without any free parameter, we explain K\pi I=3/2 S-wave phase shift very well by using t-channel rho and u-channel K^* meson exchange. With the t-channel and u-channel meson exchange fixed as the background term, we fit the K\pi I=1/2 S-wave data of the LASS experiment quite well by introducing one or two s-channel resonances. It is found that there is only one s-channel resonance between K\pi threshold and 1.6 GeV, i.e., K_0^*(1430) with a mass around 1438~1486 MeV and a width about 346 MeV, while the t-channel rho exchange gives a pole at (450-480i) MeV for the amplitude.Comment: REVTeX4 file, 11 pages and 3 figure

An autonomous chemical robot discovers the rules of supramolecular chemistry without prior knowledge

We present a chemical discovery robot for the efficient and reliable discovery of supramolecular architectures through the exploration of a huge reaction space exceeding ten billion combinations. The system was designed to search for areas of reactivity found through autonomous selection of the reagent types, amounts, and reaction conditions aiming for combinations that are reactive. The process consists of two parts where reagents are mixed together, choosing from one type of aldehyde, one amine and one azide (from a possible family of two amines, two aldehydes and four azides) with different volumes, ratios, reaction times, and temperatures, whereby the reagents are passed through a copper coil reactor. Next, either cobalt or iron is added, again from a large number of possible quantities. The reactivity was determined by evaluating differences in pH, UV‐Vis, and mass spectra before and after the search was started. The algorithm was focused on the exploration of interesting regions, as defined by the outputs from the sensors, and this led to the discovery of a range of 1‐benzyl‐(1,2,3‐triazol‐4‐yl)‐N‐alkyl‐(2‐pyridinemethanimine) ligands and new complexes: [Fe(L1)2](ClO4)2 (1); [Fe(L2)2](ClO4)2 (2); [Co2(L3)2](ClO4)4 (3); [Fe2(L3)2](ClO4)4 (4), which were crystallised and their structure confirmed by single‐crystal X‐ray diffraction determination, as well as a range of new supramolecular clusters discovered in solution using high‐resolution mass spectrometry

Correlating Heteroatoms Doping, Electronic Structures, and Photocatalytic Activities of Single‐Atom‐Doped Ag25(SR)18 Nanoclusters

Atomic‐level manipulation of catalysts is important for both fundamental studies and practical applications. Here, the central metal atom in an atomically precise Ag25 nanocluster (NC) is replaced with a single Pd, Pt, and Au atom, respectively, and employed as a model system to study the structure–property–activity relationship at the atomic level. While the geometric structures are well‐preserved after doping, the electronic structures of Ag25 NCs are significantly altered. The combination of Ag25 and TiO2 enhances the charge separation at the interface, exhibiting a 10 times higher hydrogen production rate in photocatalytic hydrogen evolution reaction compared to bare TiO2. Further results show that heteroatoms doping has a negative impact on performance, particularly in the cases of Pd and Au doping. Ultraviolet photoelectron spectroscopy measurements and density functional theory calculations suggest that the lower activities are due to an energy mismatch between the levels of doped NCs and TiO2. These findings not only reveal the impact of heteroatoms doping on the electronic properties and photocatalytic activities of NCs, but can also guide the design of heterometallic NCs for photocatalytic applications.Heteroatoms doping alters the electronic structures of Ag25 nanoclusters (NCs), while keeping the geometric structures unchanged. In this way, the geometrical effects and the electronic effects are clearly distinguished. The photocatalytic activities of as‐prepared NCs deposited onto TiO2 are investigated. The performances follow the order of Ag25 ≥ PtAg24 > PdAg24 ≥ AuAg24. image © 2023 WILEY‐VCH GmbHDFG http://dx.doi.org/10.13039/501100001659China Scholarship Council http://dx.doi.org/10.13039/501100004543Peer Reviewe