BUSCADOR RECOLECTA

The global COVID-19 spread has forced countries to implement non-pharmacological interventions (NPI) to preserve health systems. Spain is one of the most severely impacted countries, both clinically and economically. In an effort to support policy decision-making, Candel et al.(2021) [https://dx.doi.org/10.2139/ssrn.3745801] have developed a modified Susceptible-Exposed-Infectious-Removed (SEIR) epidemiological model to simulate the pandemic evolution. Its output was used to populate an economic model to quantify healthcare costs and GDP variation, through a regression model which correlates NPI and GDP change from 42 countries. The dataset contains information on the main variables used in order to specify and estimate this predictive model.

Sexually selected signals reliably reflect individual phenotypic or genetic quality and, thus, survival prospects of holders. Telomere length is considered a good predictor of life expectancy and, consequently, exploring the links between telomere length and sexually selected traits is much needed to better understand the mechanisms that maintain the honesty of sexual signals. We manipulated the length of throat feathers in spotless starling (Sturnus unicolor) males (a sexually selected signal) before reproduction and explored its effects on telomere shortening and breeding performance in subsequent reproductive events. We did not detect an effect of the feathers clipping manipulation, but males with longer throat feathers before the experiment had shorter telomeres that also shortened more slowly than those of males with shorter throat feathers did. Moreover, length of throat feathers of males before manipulation was positively related to hatching success of second clutches. Thus, correlative but not experimental results support the expected associations between sexually selected signals, telomeres and reproduction. We discuss such results in scenarios of sexual selection where feather length reflects, but does not directly cause, telomere attrition and enhanced reproductive success. Males with longer throat feathers might be older, more experienced males (i.e., with shorter telomeres), able to buffer telomere shortening between reproductive events. Because of the absence of experimental effects, differential incubation effort of females cannot explain the detected association with hatching success, but other sexually selected traits that covary with throat-feather length could be responsible. Exploring those physiological and/or morphological characteristics related to throat-feather length should therefore be the matter of future research, This work was supported by the currently named Ministerio de Ciencia, Innovación y Universidades and European (FEDER) funds (CGL2013-48193-C3-1-P, CGL2017-83103-P, CGL2017-89063-P, CGL2015-65055-P and PGC2018-095704-B-100). MAG was financed by a predoctoral contract (BES-2014-068661) from the Spanish Ministerio de Economía y Competitividad, and GT by the Ramón y Cajal Programme., Reproductive data; Telomere data, Peer reviewed

Data file includes (i) average values of melanised (M) and non-melanised (NM) feather wear of nestling birds that grew in different nests. The file also included (ii) information of feather mass degradability of nestlings and adult birds from different nests and species estimated as the olipeptide concentration (μg x mL1) of tubes containing 4mL of PBS buffer and a colony Bacillus licheniformis D13 after 21 days of incubation at 37 ºC in constant agitation at 120 rpm in an orbital agitator (VWR, Spain). The third excel sheet contain information of bacterial loads in terms of terms of mesophilic bacteria (TSA), Enterobacteriaceae (HK), Staphylococcus (VJ), and Enterococcus (KF), and average wear of melanised (M) and non-melanised (NM) wing feathers of nestlings that grew in the same nests where bacterial loads were estimated. The last excel file contain information on feather wear of melanised and non-melanised feathers of each sampled nestlings and adult. All these data were collected the Guadix region (southern Spain) and used to perform the statistical analyses in Tables 2 and 3 in Azcárate et al. 2020 (Doi: 10.1111/jav.02320)., This work was supported by the currently named Ministerio de Ciencia, Innovación y Universidades and European (FEDER) funds (CGL2013-48193-C3-1-P, CGL2013-48193-C3-2-P, CGL2013-48193-C3-3-P, CGL2017-83103-P). MAG and SDL were financed by predoctoral contracts (BES-2014-068661, BES-2014-069116) from the Spanish Ministerio de Economía y Competitividad., Peer reviewed

Study area and study species The study was conducted during the years 2015, 2016 and 2017 in a south-eastern region of Spain (Hoya de Guadix, 37º15’N, 3º01’W), where nest-boxes attached to tree trunks or walls at 3–4 m above-ground are available for starlings to breed in (for further information on the study area see Soler et al. (2017)). In the studied starling population, the reproductive season starts in early April and most individuals lay a second clutch during May-June. The most common clutch size is 62 plants to the nest, which have been shown to have antimicrobial-beneficial functions4-5 eggs. Here, we will focus on the colouration of the base of the beak, a trait with a more marked sexual differentiation as we can see in its reflectance at different wavelengths (Fig. 1). Fieldwork and experimental procedure In this population, courtship activity (e.g. singing, introducing fresh green plants and feathers in nest boxes) starts in February, more than one month before egg laying (pers. obs.). During this period, some birds roost in nest-boxes and we take advantage ofthis fact for conducting yearly bird trapping sessions in the study area (twice a year between February and mid-March). One hour before dawn, we closed the entrance of all nest boxes in the study area, and immediately after dawn, we captured by hand all individuals found roosting inside. Captured birds were kept individually in clean cotton bags hanging from a stick to keep birds quiet, and were released immediately after sampling. The maximum time that a captured starling was in the bag did never exced three hours. We explored the possible effect of time that birds were kept in the bag on bird colouration and body condition measures of the males that we recaptured by classifying them as being kept in the bag less than 1 hour (N(males) = 10), between 1 and 2 hours (N = 5), and between 2 and 3 hours (N = 7). After controlling for the effect of date of first and last capture, time between captures, treatment and size of throat feathers in the first capture, results showed that retaining time 184 in first captures did not significantly affect blue, red-yellow, or brightness colouration of the beak of males (F1,15 < 2.66, P > 0.124), nor body condition (F1, 10 = 2.19, P = 0.170) in subsequent captures. It neither had any apparent long-term consequences (see Ruiz-Rodríguez et al. (2015)), nor imply apparent negative effects on breeding performance of captured birds (Soler et al. 2008), This work was supported by the currently named Ministerio de Ciencia,es and European (FEDER) funds (GL2013C-48193-C3-1-P, CGL2017-83103-P Innovación Universidad, CGL2017-89063-P). MAG was financed by a predoctoral contract (BES-2014-068661) from the Spanish Ministerio de Economía y Competitividad, and GT by the Ramón y Cajal Programme, Peer reviewed

Dataset used in Tomás et al. (2020): (DOI: 10.1111/jav.02427). Data were collected in the Hoya de Guadix in 2012 in spotless starling (Sturnus unicolor) nests in the framework of an experiment to evaluate whether distance to the cavity entrance and nest size influence the risk of ectoparasitism in avian nests. Dataset includes hatching date, brood size, mean nestling body mass, microclimate of the cavity, as well as ectoparasite abundance and distance between the nest and the cavity entrance before and after experimental manipulation., Dataset used in Tomás et al. (2020): (DOI: 10.1111/jav.02427). It contains data collected in Guadix in 2012 in the framework of an experiment to evaluate whether distance to the cavity entrance and nest size influence the risk of ectoparasitism in avian nests., Financial support was provided by grants from Spanish Ministerio de Ciencia e Innovación (MCI) and FEDER (CGL2010-19233-C03-01), from Ministerio de Economía, Industria y Competitividad (CGL2017-89063-P, CGL2017-83103-P), by a predoctoral fellowship from MCI to CRC, by Junta para Ampliación de Estudios programme to MRR, and by Juan de la Cierva and Ramón y Cajal programmes to GT., Peer reviewed