Un nuevo grupo de manos paleolíticas pintadas en el sur de la Península Ibérica. La cueva de las Estrellas (Castellar de la Frontera, Cádiz)

Presentamos en este trabajo la revisión de las manifestaciones de arte rupestre conservadas en una estación localizada en la comunidad autónoma de Andalucía, conocida en la literatura precedente como cueva de Las Estrellas (Castellar de la Frontera, Cádiz). Se trata de un abrigo rocoso de grandes dimensiones, abierto al aire libre, en el que ya se había constatado, en los primeros años del presente siglo, la presencia de diversas pictografías de estilo esquemático. Durante una visita reciente al enclave se ha advertido, además, la existencia de un importante conjunto figurativo de cronología paleolítica que incluye representaciones de fauna y una pequeña serie de improntas de manos en negativo. Este artículo aborda el análisis genérico de las grafías catalogadas hasta el momento en la cavidad, atendiendo con especial detalle al conjunto de las citadas huellas de manos paleolíticas, que han sido documentadas usando tecnología digital 3d. De igual modo, se tendrán en cuenta su contextualización en el arte paleolítico andaluz y una primera aproximación cronológica a este interesante y variado complejo figurativo

Gaia Early Data Release 3: The celestial reference frame (Gaia-CRF3)

Context. Gaia-CRF3 is the celestial reference frame for positions and proper motions in the third release of data from the Gaia mission, Gaia DR3 (and for the early third release, Gaia EDR3, which contains identical astrometric results). The reference frame is defined by the positions and proper motions at epoch 2016.0 for a specific set of extragalactic sources in the (E)DR3 catalogue. Aims. We describe the construction of Gaia-CRF3 and its properties in terms of the distributions in magnitude, colour, and astrometric quality. Methods. Compact extragalactic sources in Gaia DR3 were identified by positional cross-matching with 17 external catalogues of quasi-stellar objects (QSO) and active galactic nuclei (AGN), followed by astrometric filtering designed to remove stellar contaminants. Selecting a clean sample was favoured over including a higher number of extragalactic sources. For the final sample, the random and systematic errors in the proper motions are analysed, as well as the radio-optical offsets in position for sources in the third realisation of the International Celestial Reference Frame (ICRF3). Results. Gaia-CRF3 comprises about 1.6 million QSO-like sources, of which 1.2 million have five-parameter astrometric solutions in Gaia DR3 and 0.4 million have six-parameter solutions. The sources span the magnitude range G = 13-21 with a peak density at 20.6 mag, at which the typical positional uncertainty is about 1 mas. The proper motions show systematic errors on the level of 12 μas yr-1 on angular scales greater than 15 deg. For the 3142 optical counterparts of ICRF3 sources in the S/X frequency bands, the median offset from the radio positions is about 0.5 mas, but it exceeds 4 mas in either coordinate for 127 sources. We outline the future of Gaia-CRF in the next Gaia data releases. Appendices give further details on the external catalogues used, how to extract information about the Gaia-CRF3 sources, potential (Galactic) confusion sources, and the estimation of the spin and orientation of an astrometric solution

Dietary α‐Linolenic Acid, Marine ω‐3 Fatty Acids, and Mortality in a Population With High Fish Consumption: Findings From the PREvención con DIeta MEDiterránea (PREDIMED) Study

Background: Epidemiological evidence suggests a cardioprotective role of α‐linolenic acid (ALA), a plant‐derived ω‐3 fatty acid. It is unclear whether ALA is beneficial in a background of high marine ω‐3 fatty acids (long‐chain n‐3 polyunsaturated fatty acids) intake. In persons at high cardiovascular risk from Spain, a country in which fish consumption is customarily high, we investigated whether meeting the International Society for the Study of Fatty Acids and Lipids recommendation for dietary ALA (0.7% of total energy) at baseline was related to all‐cause and cardiovascular disease mortality. We also examined the effect of meeting the society's recommendation for long‐chain n‐3 polyunsaturated fatty acids (≥500 mg/day). Methods and Results: We longitudinally evaluated 7202 participants in the PREvención con DIeta MEDiterránea (PREDIMED) trial. Multivariable‐adjusted Cox regression models were fitted to estimate hazard ratios. ALA intake correlated to walnut consumption (r=0.94). During a 5.9‐y follow‐up, 431 deaths occurred (104 cardiovascular disease, 55 coronary heart disease, 32 sudden cardiac death, 25 stroke). The hazard ratios for meeting ALA recommendation (n=1615, 22.4%) were 0.72 (95% CI 0.56–0.92) for all‐cause mortality and 0.95 (95% CI 0.58–1.57) for fatal cardiovascular disease. The hazard ratios for meeting the recommendation for long‐chain n‐3 polyunsaturated fatty acids (n=5452, 75.7%) were 0.84 (95% CI 0.67–1.05) for all‐cause mortality, 0.61 (95% CI 0.39–0.96) for fatal cardiovascular disease, 0.54 (95% CI 0.29–0.99) for fatal coronary heart disease, and 0.49 (95% CI 0.22–1.01) for sudden cardiac death. The highest reduction in all‐cause mortality occurred in participants meeting both recommendations (hazard ratio 0.63 [95% CI 0.45–0.87]). Conclusions: In participants without prior cardiovascular disease and high fish consumption, dietary ALA, supplied mainly by walnuts and olive oil, relates inversely to all‐cause mortality, whereas protection from cardiac mortality is limited to fish‐derived long‐chain n‐3 polyunsaturated fatty acids. Clinical Trial Registration URL: http://www.Controlled-trials.com/. Unique identifier: ISRCTN35739639

Gaia Data Release 3: reflectance spectra of Solar System small bodies

Stars and planetary system

Gaia Data Release 3: the extragalactic content

Galaxie

Gaia Data Release 3: mapping the asymmetric disc of the Milky Way

Galaxie

Whole-genome sequencing reveals host factors underlying critical COVID-19

Critical COVID-19 is caused by immune-mediated inflammatory lung injury. Host genetic variation influences the development of illness requiring critical care1 or hospitalization2,3,4 after infection with SARS-CoV-2. The GenOMICC (Genetics of Mortality in Critical Care) study enables the comparison of genomes from individuals who are critically ill with those of population controls to find underlying disease mechanisms. Here we use whole-genome sequencing in 7,491 critically ill individuals compared with 48,400 controls to discover and replicate 23 independent variants that significantly predispose to critical COVID-19. We identify 16 new independent associations, including variants within genes that are involved in interferon signalling (IL10RB and PLSCR1), leucocyte differentiation (BCL11A) and blood-type antigen secretor status (FUT2). Using transcriptome-wide association and colocalization to infer the effect of gene expression on disease severity, we find evidence that implicates multiple genes—including reduced expression of a membrane flippase (ATP11A), and increased expression of a mucin (MUC1)—in critical disease. Mendelian randomization provides evidence in support of causal roles for myeloid cell adhesion molecules (SELE, ICAM5 and CD209) and the coagulation factor F8, all of which are potentially druggable targets. Our results are broadly consistent with a multi-component model of COVID-19 pathophysiology, in which at least two distinct mechanisms can predispose to life-threatening disease: failure to control viral replication; or an enhanced tendency towards pulmonary inflammation and intravascular coagulation. We show that comparison between cases of critical illness and population controls is highly efficient for the detection of therapeutically relevant mechanisms of disease

Genetic structure of four Spanish sheep breeds using a SNP-chip

Modern genomic tools allow genome-wide association studies (GWAS) to find genes underlying economically important traits in animals. In human, these studies have found many associations that cannot be always replicated. One of the reasons for this is the presence of population stratification in groups considered to be homogeneous. The objective of this work was to study the genetic structure of four Spanish sheep breeds (Castellana, Churra, Ojalada and Rasa Aragonesa) included in the Sheep HapMap. We selected 154 SNPs from the Ovine SNP50BeadChip, using PLINK options. Five independent analyses were made with STRUCTURE software to calculate the most likely number of clusters. The closest breeds were Ojalada and Rasa Aragonesa; Awassi was the most different when compared with any of the Spanish breeds. Population structure analysis revealed K=6 to be the most likely number of clusters. According to these results, Awassi was the most different breed (K=2), whereas among the Spanish populations, Churra was the only one clustering separately from the rest (K=3). Moreover, there were more differences within this breed than among the others (K=6). This study represents a first approach to assess/study population structure in Spanish sheep breeds and understand how these populations will behave in future GWA

Changes in the microbiome composition in Churra sheep with a resistant phenotype to infection

Trabajo presentado al: COMBAR meeting (Combatting Anthelmintic Resistance in Ruminants). Atenas (Grecia). Febrero. 2022

Analysis of the usefulness of ovine SNP50BeadChip (Illumina) for genomic studies in Spanish sheep breeds

During the development of the Sheep HapMap project, ewes from 6 breeds (Awassi, Merino, Poll Dorset, Romney, Scottish Blackface and Texel) were used to obtain the sequence of the ovine genome and look for variability. The Ovine SNP50BeadChip (Illumina) was then genotyped in 71 breeds, four of which were Spanish breeds. In some species (pig and cow) a bias has been described when testing a SNP Chip in different breeds. The aim of this study was to analyse this possible bias due to the sheep breed in the Spanish populations included in the Sheep HapMap project. For this purpose, we estimated for both, the breeds used in the Chip development and the Spanish populations the following parameters: MAF within and between breeds, gene diversity, individual heterozygosity and average proportion of alleles shared within population. The results obtained in Spanish breed were similar to those observed in the six breeds sequenced during the SNP-chip development. These findings support the value of Ovine SNP50BeadChip for genomic analysis in Spanish sheep breeds