Spanish Ministerio De Ciencia Research Articles

Role of the first WHO mutation catalogue in the diagnosis of antibiotic resistance in Mycobacterium tuberculosis in the Valencia Region, Spain: a retrospective genomic analysis

In June, 2021, WHO published the most complete catalogue to date of resistance-conferring mutations in Mycobacterium tuberculosis. Here, we aimed to assess the performance of genome-based antimicrobial resistance prediction using the catalogue and its potential for improving diagnostics in a real low-burden setting. In this retrospective population-based genomic study M tuberculosis isolates were collected from 25 clinical laboratories in the low-burden setting of the Valencia Region, Spain. Culture-positive tuberculosis cases reported by regional public health authorities between Jan 1, 2014, and Dec 31, 2016, were included. The drug resistance profiles of these isolates were predicted by the genomic identification, via whole-genome sequencing (WGS), of the high-confidence resistance-causing variants included in the catalogue and compared with the phenotype. We determined the minimum inhibitory concentration (MIC) of the isolates with discordant resistance profiles using the resazurin microtitre assay. WGS was performed on 785 M tuberculosis complex culture-positive isolates, and the WGS resistance prediction sensitivities were: 85·4% (95% CI 70·8-94·4) for isoniazid, 73·3% (44·9-92·2) for rifampicin, 50·0% (21·1-78·9) for ethambutol, and 57·1% (34·0-78·2) for pyrazinamide; all specificities were more than 99·6%. Sensitivity values were lower than previously reported, but the overall pan-susceptibility accuracy was 96·4%. Genotypic analysis revealed that four phenotypically susceptible isolates carried mutations (rpoB Leu430Pro and rpoB Ile491Phe for rifampicin and fabG1 Leu203Leu for isoniazid) known to give borderline resistance in standard phenotypic tests. Additionally, we identified three putative resistance-associated mutations (inhA Ser94Ala, katG Leu48Pro, and katG Gly273Arg for isoniazid) in samples with substantially higher MICs than those of susceptible isolates. Combining both genomic and phenotypic data, in accordance with the WHO diagnostic guidelines, we could detect two new multidrug-resistant cases. Additionally, we detected 11 (1·6%) of 706 isolates to be monoresistant to fluoroquinolone, which had been previously undetected. We showed that the WHO catalogue enables the detection of resistant cases missed in phenotypic testing in a low-burden region, thus allowing for better patient-tailored treatment. We also identified mutations not included in the catalogue, relevant at the local level. Evidence from this study, together with future updates of the catalogue, will probably lead in the future to the partial replacement of culture testing with WGS-based drug susceptibility testing in our setting. European Research Council and the Spanish Ministerio de Ciencia.

(Invited) tamm Plasmon Resonance Sensors Based on Nanoporous Anodic Alumina Photonic Crystals

Nanoporous Anodic Alumina (NAA) is a material with growing interest in nanotechnology and for biological and medical applications. It is a cost-effective nanostructured material obtained by the electrochemical etching of aluminum in acidic electrolytes at the adequate conditions of applied voltage or current, temperature and electrolyte composition [1-4]. The precise control over the diameter of the nanopore allows to create periodic variations of nanopore’s diameter in deep and obtain different photonic crystals e.g.., Gradient-index filters, microcavities, Distributed Bragg Reflectors, etc [5-6]. The optical properties of NAA depend on its nanoporous structure and of its functionalized surface. NAA can be used to fabricate hybrid photonic structures by gold coating on nanoporous anodic alumina photonic crystals surface (NAA-PCs) [7]. In this metal-dielectric photonic structure, we can observe effects of an enhancement of the surface plasmon resonance due to absorption of the light at the interface of metallic layer and the NAA photonic crystal.Tamm plasmon resonance (TPR) can be tuned by engineering the properties and characteristics of the metal film and the porous photonic structure, providing new opportunities to achieve unique plasmonic−photonic structures for different applications (optical switching, lasing, light emission, surface-enhanced spectroscopy, and sensing). One interesting application of TPR is the use as a sensing platform taking advantage of its exceptional optical properties to confine/amplify the light-matter interactions [8-9]. The sensing performance of TPR-NAA−PCs is assessed by the infiltration of their structure with analytical solutions, producing a spectral shift in the Tamm plasmonic resonance. In this work, we evaluate the structural geometry and the optical properties of TPR-NAA-PCs and the assessment of TPR-NAA-PCs as a sensing platform.Figure 1a shows the reflectance spectrum for a TPR-NAA–PCs structure. The spectrum shows the photonic bandgap and the absorption narrow-line associated with the resonant recirculation of light within the plasmon-photonic system. Figure 1b shows the sensing performance of TPR-NAA-PCS. Red-shift on the position of the TPR-NAA-PCs is observed due to the refractive index variation when the nanopores are infiltrated of different analytical solutions (water- ethylene glycol)AcknowledgmentsThis work was supported by the Spanish Ministerio de Ciencia e Innovación (MICINN/FEDER) PDI2021- 128342OB-I00, by the Agency for Management of University and Research Grants (AGAUR) ref. 2017- SGR-1527, COST Action 20126 - NETPORE and by the Catalan Institution for Research and Advanced Studies (ICREA) under the ICREA Academia Award.

Synthesis and Excited State Charge Separation Involving Coordinated C60 of π-Extended Pyrazinepyrene Fused Zinc Phthalocyanines

Polycyclic aromatic hydrocarbons (PAHs) play an important role in organic electronics.[1] To increase the stability and the conjugation, pyrene units could be further attached through heteroatoms to improve the photo/chemical stability to oxygen or light.[2] In terms of the synthesis of these types of large acenes through pyrene, many routes have been studied and one of the best protocols is to synthesize the quinoxaline derivative from the dione and the corresponding diamino subunit.[3] Herein, we will present a series of pyrazinepyrene fused zinc phthalocyanines (ZnPc-Pyrn) as a new class of π-extended phthalocyanine systems. Bathochromically shifted absorption as a function of the number of pyrazinepyrene entities due to extended π-conjugation, and quenched fluorescence due to the presence of fused pyrazinepyrene were witnessed. The electronic structures of these phthalocyanines were probed by systematic computational and electrochemical studies while the excited state properties were examined by pump-probe spectroscopies operating at the femto- and nanosecond time scales. Like the excited singlet lifetimes, the excited triplet states also revealed diminished lifetimes with an increased number of pyrazinepyrene entities. Further, the coordinatively unsaturated zinc in these molecules was coordinated with phenyl imidazole functionalized fullerene, ImC60 to form a new series of donor-acceptor conjugates. Upon full characterization of these conjugates, the occurrence of excited-state charge separation was established by transient pump-probe spectroscopy covering wide temporal and spatial regions. With an increase in pyrazinepyrene entities, an increased rate of forward charge separation was witnessed while rate constants for charge recombination were slower resulting in the final lifetime of charge-separated states of about 40-50 ns, better than that reported earlier for a similar pristine zinc phthalocyanine derived dyad. [4]AcknowledgmentsAuthors acknowledge the support from the Spanish Ministerio de Ciencia e Innovación (MICINN/FEDER, PID2020-117855RB-I00 to ASS) and Generalitat Valenciana (CIPROM/2021/059 and MFA/2022/028 to ASS) and US-National Science Foundation (2000988 to FD). The computational work was completed at the Holland Computing Center of the University of Nebraska, which receives support from the Nebraska Research Initiative.

Hub Location with Protection Under Interhub Link Failures

This paper introduces the hub location problem under interhub link failures, a hub location problem in which activated interhub links may fail with a given probability. Two different optimization models are studied, which construct hub backbone networks protected under interhub link disruptions by imposing that, for each commodity, an additional routing path exists besides its original routing path. Both models consider the minimization of the fixed costs of the activated hubs and interhub links plus the expected value of the routing costs of the original and alternative paths. The first model builds explicitly the alternative routing paths, whereas the second model guarantees that, for each commodity, at least one alternative path exists using a large set of connectivity constraints although the alternative paths are not built explicitly. The results of extensive computational testing allow us to analyze the performance of the two proposed models and to evaluate the extra cost required to design a robust backbone network under interhub link failures. The obtained results support the validity of the proposal. History: Accepted by David Alderson, Area Editor for Network Optimization: Algorithms & Application. Funding: The authors of this research acknowledge financial support by the Spanish Ministerio de Ciencia y Tecnología, Agencia Estatal de Investigación and Fondos Europeos de Desarrollo Regional (FEDER) via projects PID2020-114594GB-C21 and MTM2019-105824GB-I00. The authors also acknowledge partial support from projects FEDER-US-1256951, Junta de Andalucía P18-FR-422, P18-FR-2369, B-FQM-322-UGR20 (COXMOS), and NetmeetData: Ayudas Fundación BBVA a equipos de investigación científica 2019. The first author was partially supported by the IMAG-Maria de Maeztu grant [CEX2020-001105-M/AEI/10.13039/501100011033] and UE-NextGenerationEU (ayudas de movilidad para la recualificación del profesorado universitario). Supplemental Material: The online supplement is available at https://doi.org/10.1287/ijoc.2023.1296 .

Review of Juan José Martínez Sierra (Ed.) (2021). Multilingualism, Translation and Language Teaching. The PluriTAV Project. Tirant lo Blanch

The book Multilingualism, Translation and Language Teaching, The PluriTAV Projec, edited by Juan José Martínez Sierra stems from the PluriTav Project funded by the Spanish Ministerio de Ciencia e Innovación and led by researchers at the Universitat de València, Universitat Jaume I, University College London, and the University of Roehampton. The book is divided into 13 chapters within two distinct parts. Part 1 consists of 5 chapters and presents the project rationale, the research and teaching context in which it emerged, its findings, and learning and teaching materials created by project members. Part 2 comprises 8 chapters, each of them featuring a research paper amongst the papers presented at the PluriTAV International Conference Multilingualism, Translation, and Language Teaching, which was held in Valencia, Spain, in 2019. The book is prefaced by an introductory chapter written by the editor and concludes with some final remarks.

(Invited, Digital Presentation) Translational Multiplexed Electroanalytical Biotools for Assisting Personalized Diagnosis and Follow-up of Known or Unexpected Diseases

The evolution of human diseases involves a highly dynamic and interactive system of multiple layers of molecular markers. Therefore, it is now fully accepted that simultaneous analysis of molecular markers from the same or different omics layers leads to novel strategies for their realistic early detection and monitoring, thus improving disease prevention, treatment, and outcomes. In this regard, features such as versatility for profiling multiple and/or multi-omics biomarkers, simplicity, affordable cost, markedly shorter analysis time and smaller sample amount required for analyses compared to conventional or state-of-the-art methodologies, make electrochemical bioplatforms suitable alternatives for routine determinations in clinical and basic research settings. The great advances demonstrated by electrochemical biosensors in recent years have gone hand in hand with the development of new electrochemical substrates, attractive surface chemistries, bioassay formats and amplification strategies, but also with the production and application of new bioreceptors, such as those provided by HaloTag and Phage Display technologies, which has allowed these devices to incur and demonstrate pioneering applications.With all this in mind, this communication will discuss bioelectroanalytical tools recently developed by us and our partners potentially transferable to the clinic due to their simplicity, cost, testing time and decentralized character, which have shown pioneering applications to decisively aid in personalized diagnostics by targeting methylation events in nucleic acids both globally and regionally and deregulated autoantibody expression.These biotools have shown to be able to determine simultaneously and with monobasic sensitivity the most common methylated bases in nucleic acids: 5-methylcytosine 5-mC), 5-hydroxymethylcytosine (5-hmC) and N6-methyladenine (6mA) in DNA and N6-methyladenosine (m6A) in RNA, both globally and regionally and without adopting other amplification strategies than conventional enzymatic labeling [1,2]. A multiplexed platform was proposed with application to the global determination of m6A in total RNA extracted from colorectal cancer cells with different metastatic potential, and to the determination of global methylations of 5-mC, 5-hmC and 6mA in genomic DNA extracted from matched tumor and healthy tissues of CRC patients. The obtained results demonstrated the clinical potential of the developed multiplexed bioplatform to discriminate the aggressiveness of tumor cells as well as tumor versus healthy tissues (accuracy, sensitivity, and specificity of 87.5, 100 and 75 %, respectively, using Ward's clustering method) in only 45 min from small amounts (no more than 100 ng) of denatured genomic DNA and crude total RNA without fragmentation and amplification.As for the electroanalytical bioplatforms developed for autoantibodies determination, they have shown ability to identify and confirm the clinical potential of previously undescribed specific autoantibody signatures against i) tumor-associated antigens, identified in the circulation or in tumor exosomes, for early and differential diagnosis of a given neoplasm [3,4]; ii) phage-derived and aberrant HaloTagged peptides to diagnose Alzheimer's disease (AD) [5]; and iii) SARS-CoV-2 serum-specific immunoglobulins to identify vulnerable population or with natural or acquired immunizations, allowing early detection of exaggerated immune system responses or epidemiological studies on the strain responsible for the infection and the efficacy of available vaccines against the different variants of the virus.It is exciting and rewarding to think that we are tackling and developing highly versatile technologies with the potential to efficiently provide relevant information on key aspects of known and unexpected diseases, such as their onset, severity, and immune response, enabling their management in a fast, simple, affordable, and personalized way in diverse settings.[1] Povedano et al. Anal. Chem. 92 (2020) 5604−5612.[2] Povedano et al. Anal. Chim. Acta 1182 (2021) 338946. https://doi.org/10.1016/j.aca.2021.338946.[3] Garranzo-Asensio et al. Theranostics 10(7) (2020) 3022–3034.[4] Montero-Calle et al. Engineering (2021) in press. https://doi.org/10.1016/j.eng.2021.04.026.[5] Valverde et al. Analysis & Sensing 1 (2021) 161-165.The financial support of PID2019-103899RB-I00 (Spanish Ministerio de Ciencia e Innovación), Research Project, PI17CIII/00045 and PI20CIII/00019 grants from the AES-ISCIII program grants from the AES-ISCIII program and the TRANSNANOAVANSENS-CM Program from the Comunidad de Madrid (Grant S2018/NMT-4349) are gratefully acknowledged.

The long period of 3He-rich solar energetic particles measured by Solar Orbiter 2020 November 17-23

The Suprathermal Ion Spectrograph (SIS) is a European facility instrument funded by ESA. The SIS instrument was constructed by the JHU/Applied Physics Lab. and CAU Kiel. We thank the many individuals at ESA and within the Energetic Particle Detector team for their support in its development. Post launch operation of SIS at APL is funded by NASA contract NNN06AA01C, and we thank NASA headquarters and the NASA/GSFC Solar Orbiter project office for their continuing support. The UAH team acknowledges the financial support by the Spanish Ministerio de Ciencia, Innovacion y Universidades FEDER/MCIU/AEI Projects ESP2017-88436- R and PID2019-104863RB- I00/AEI/10.13039/501100011033. The CAU Kiel team thanks the German Federal Ministry for Economic Affairs and Energy and the German Space Agency (Deutsches Zentrum fur Luft- und Raumfahrt, e.V., (DLR)) for their unwavering support under grant numbers 50OT0901, 50OT1202, 50OT1702, and 50OT2002; and ESA for supporting the build of SIS under contract number SOL.ASTR.CON.00004, and the University of Kiel and the Land Schleswig-Holstein for their support of SIS. R. Bucik is supported ˇ in part by NASA grant 80NSSC19K0079. F. Carcaboso acknowledges the financial support by the Spanish MINECO-FPI-2016 predoctoral grant with FSE. V. Krupaˇr acknowledges the support by NASA under grants 18-2HSWO2182- 0010 and 19-HSR-192-0143. L. Balmaceda acknowledges the support from the NASA program NNH17ZDA001N-LWS (Awards Nr. 80NSSC19K1261 and 80NSSC19K1235).

Access to Gold(I) Protic N-Heterocyclic Carbene Complexes from Trinuclear Gold(I) Imidazolate Clusters

This work was supported by the Spanish Ministerio de Ciencia e Innovacion (Project No. PID2019-109975GB-100) and the University of Oviedo (Project Nos. PAPI-20-PUENTE-10 and PAPI-20-GR-2011-0027). M.A.M. thanks the MINECO for a scholarship. This article is dedicated to the memory of Professor Victor Riera and in honor to his many contributions to organometallic chemistry.

Elsepa—Dirac partial-wave calculation of elastic scattering of electrons and positrons by atoms, positive ions and molecules (New Version Announcement)

A new version of the Fortran program elsepa, which calculates differential and integrated cross sections for elastic scattering of electrons and positrons, is presented. Details of the program and its applications are given in the original paper [Comput. Phys. Commun.165 (2005) 157–190]. Dirac phase shifts are now calculated by using the recently published subroutine package radial (Salvat and Fernández-Varea, 2019), which solves the radial wave equation for real or complex central potentials by means of a robust and accurate power-series method. In addition, elastic collisions with atoms in elemental solids are described by using the muffin-tin optical model potential proposed by Bote et al., (2009), which is somewhat more elaborate and flexible than that in the original elsepa code and allows adjusting the absorption potential to give inelastic cross sections in close agreement with empirical data. With the use of the radial subroutines, the work of elsepa is reduced to (1) the definition of the interaction potential and (2) the summation of the partial-wave series of the scattering amplitudes. The structure of the new code has been simplified and stricter criteria for the convergence of the partial-wave series have been adopted. The distribution package includes gnuplot scripts for easy visualization of the calculation results. Program summaryProgram Title:elsepaCPC Library link to program files:https://doi.org/10.17632/w4hm5vymym.1Licensing provisions: CC BY NC 3.0Programming language: Fortran 90Journal reference of previous version: Comput. Phys. Commun. 165 (2005) 157–190Does the new version supersede the previous version?: YesReasons for the new version: This new version offers increased accuracy, and a more flexible modeling of elastic collisions of electrons and positrons with atoms in elemental solids.Summary of revisions: The calculation of phase shifts is now performed by the generic subroutines of the radial package [1]. A more flexible optical-model potential for scattering in solids is included [2]. Stricter criteria for convergence of the partial-wave series are applied. The distribution package has been reorganized, with the numerical database files now placed in a separate directory; scripts for direct visualization of the calculation results with the plotting program gnuplot (http://www.gnuplot.info) are also included.Nature of problem: The code calculates differential cross sections, total cross sections and transport cross sections for single elastic scattering of electrons and positrons by neutral atoms, positive ions and randomly oriented molecules. When the energy of the projectile is less than about 5 MeV, the programs also compute scattering amplitudes and spin polarization functions.Solution method: The effective interaction between the projectile and the target atom is represented by a local central potential that can optionally include an imaginary (absorptive) part to account approximately for the coupling with inelastic channels. For projectiles with kinetic energy less that about 5 MeV, the code performs a conventional relativistic Dirac partial-wave analysis. For higher kinetic energies, where the convergence of the partial-wave series is too slow, approximate factorization methods are used. The programs only admit kinetic energies higher than 5 eV, a practical lower limit that may be changed by editing the source files.Additional comments including restrictions and unusual features: The calculations are based on the static-field approximation. The optional correlation-polarization and inelastic absorption corrections are obtained from approximate, semi-empirical models. elsepa allows considering an absorption potential only for projectiles with energies less than about 1 MeV; for higher energies, the absorption potential is set to zero to prevent the occurrence of numerical instabilities. Calculations for molecules are based on a single-scattering independent-atom approximation. To ensure accuracy of the results for scattering by ions, the electron density of the ion must be supplied by the user; it can be generated, e.g., by running the program dhfs of the radial package [1].AcknowledgmentsWe are indebted to Dr John Villarrubia for pointing out various cases of incomplete convergence of the original code. Financial support from the Spanish Ministerio de Ciencia, Innovación y Universidades / Agencia Estatal de Investigación, Spain / European Regional Development Fund , European Union, (project no. RTI2018-098117-B-C22) is gratefully aknowledged.

Incidence and genetic diversity of cucurbit viruses in Spain

This study was partially supported by the Spanish Ministerio de Ciencia, Innovacion y Universidades grants AGL2017-85563-C2 (1-R and 2-R) and RTA2017-00061-C03-03 (INIA) cofounded with FEDER funds, and by the PROMETEO project 2017/078 (to promote excellence groups) by the Conselleria d'Educacio , Investigacio , Cultura i Esports (Generalitat Valenciana). C. Saez is a recipient of a predoctoral fellowship (ACIF/2016/188) from Generalitat Valenciana, cofunded by the Operational Program of the European Social Fund (FSECV 2014-2020).

Beating the Thermal Conductivity Alloy Limit Using Long-Period Compositionally Graded Si1–xGex Superlattices

The Spanish Ministerio de Ciencia, Innovacion y Universidades, is gratefully acknowledged for its support through Grant No. SEV-2015-0496 in the framework of the Spanish Severo Ochoa Centre of Excellence program and through Grants MAT2016-79759-R (PHONTANNA), MAT2015-70850-P (HIBRI2), and CSD2010-00044 (Consolider NANOTHERM). The authors also thank the Catalan agency AGAUR for Grant 2017-SGR-00488.

Radical Arylation of Triphenyl Phosphite Catalyzed by Salicylic Acid: Mechanistic Investigations and Synthetic Applications.

A straightforward and scalable methodology to synthesize diphenyl arylphosphonates at 20 °C within 1-2 h is reported using inexpensive SA as the catalytic promoter of the reaction. Mechanistic investigations suggest that the reaction proceeds via radical-radical coupling, consistent with the so-called persistent radical effect. The reaction tolerated a wide range of functional groups and heteroaromatic moieties. The synthetic usefulness and the unique reactivity of the obtained phosphonates were demonstrated in different one-step transformations.

VOFTools 5: An extension to non-convex geometries of calculation tools for volume of fluid methods

VOFTools 5: An extension to non-convex geometries of calculation tools for volume of fluid methods

Correction to “Tear-and-Interconnect Domain Decomposition Scheme for Solving Multiscale Composite Penetrable Objects”

In the above article [1] , the paragraph of support information, sponsor, and financial support acknowledgment should read “This work was supported in part by the European Regional Development Fund (ERDF) and the Spanish Ministerio de Ciencia, Innovacioin y Universidades under Project TEC2017-85376-C2-1-R and Project TEC2017-85376-C2-2-R, in part by the ERDF and the Galician Regional Government as part of the agreement for funding the Atlantic Research Center for Information and Communication Technologies (AtlantTIC), and in part by the ERDF and the Extremadura Regional Government under Project IB18073 and Project GR18055.”

Electric-field-induced avalanches and glassiness of mobile ferroelastic twin domains in cryogenic SrTiO3

We acknowledge financial support from EPSRC (Grant No. EP/P024904/1) and support from the Spanish Ministerio de Ciencia, Innovacion y Universidades through Grant No. MAT2017-85232-R (AEI/FEDER, EU), Severo Ochoa SEV-2015-0496, the Generalitat de Catalunya through Grant No. 2017 301 SGR1377, and the Academy of Finland (Grant No. 316857).

Surface electronic structure of the wide band gap topological insulator PbBi4Te4Se3

This work is supported by the Russian Science Foundation (Grants No. 18-12-00169 in part of the density functional calculations and No. 18-12-00062 in part of the photoemission measurements) and Saint Petersburg State University (Grant ID 40990069). The support from the Academic D.I. Mendeleev Fund Program of Tomsk State University (Project No. 8.1.01.2018), the Russian Foundation for Basic Researches (Grant No. 18-52-06009), the Science Development Foundation under the President of the Republic of Azerbaijan (Grant No. EIF/MQM/Elm-Tehsil-1-2016-1(26)-71/01/4-M33), the Basque Country Government, Departamento de Educacion, Universidades e Investigacion (Grants No. IT-756-13 and No. IT1301-19) and the Spanish Ministerio de Ciencia e Innovacion (Grant No. FIS2016-75862-P) are acknowledged. J.S.-B. gratefully acknowledges financial support from the Impuls-und Vernetzungsfonds der Helmholtz-Gemeinschaft under Grant No. HRSF-0067 (Helmholtz-Russia Joint Research Group). Calculations were partly performed using computational resources provided by Resource Center “Computer Center of SPbU” (http://cc.spbu.ru) and the SKIFCyberia sup

More than an Artist in the Making: Samuel Beckett’s “Assumption” Revisited

Abstract Samuel Beckett’s first published short story, “Assumption” (1929), is usually described as an apprentice work, “a piece of marginally interesting juvenilia” (Pattie 2000: 52), a beginner’s attempt toward a modernist short story in which the influence of James Joyce is clear. Indeed, it has been claimed that Joyce’s A Portrait of the Artist as a Young Man is the model underlying Beckett’s early foray into creative fiction. The current paper seeks to reassess the established critical appreciation of “Assumption”, that of being a parody of Joyce’s novel by a playful disciple; instead, I will argue that Beckett was in fact questioning the very principles of his master’s art. If Portrait is the epitome of the Künstlerroman, Beckett in his short piece debunked the myth of the young artist by consciously downgrading the aesthetic concerns of his protagonist and by disrupting the revered categories of modernist fiction.This essay is part of the research project FF I 2016-76477-P, funded by the Spanish Ministerio de Ciencia, Innovación y Universidades and by AEI / FEDER. The author would also like to thank CEI Patrimonio (Universidad de Almería) for their support..

Erratum: Supergranular turbulence in the quiet Sun: Lagrangian coherent structures

SSAS acknowledges financial support from agency Coordenacao de aperfeicoamento de Pessoal de nivel Superior (CAPES 88882.316962/2019-01, Brazil). ELR acknowledges financial support from Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq, Brazil), partial financial support from CAPES (Brazil) and from Fundacao de Amparo a Pesquisa de Sao Paulo (FAPESP, Brazil). LBR acknowledges financial support from the Spanish Ministerio de Ciencia, Innovacion y Universidades through grant RTI2018-096886-B-C51, including a percentage from European Regional Development Fund (FEDER), and through the 'Center of Excellence Severo Ochoa' award to the Instituto de Astrofisica de Andalucia (SEV-2017-0709).

VOFTools 3.2: Added VOF functionality to initialize the liquid volume fraction in general convex cells

VOFTools 3.2: Added VOF functionality to initialize the liquid volume fraction in general convex cells

Nest material preferences by spotless starlings

This work was supported by Spanish Ministerio de Ciencia e Innovacion, European funds (FEDER) (CGL2010-19233-C03-01, CGL2010-19233-C03-03, CGL2013-48193-C3-1-P, CGL2013-48193-C3-2-P). M.R.R. received a postdoc from the program “JAE-Doc” and C.R.C. had a predoctoral grant from the Spanish Government. G.T. was supported by Ramon y Cajal program (Spain).