BUSCADOR RECOLECTA

1. Batch fluidized bed methodology: The following methodology was used during the fluidized bed testing: i. The reactor was heated up in an N2 stream of 850 ml/min at a rate of 20 °C /min until the OC started to release O2, then the gas was switched to 11 vol% of O2 with N2 for balance. Note that the same mixture of air and N2 was used to regenerate the oxygen carrier (OC) after the Chemical Looping Oxygen Uncoupling (CLOU) and syngas reactions. Once the temperature and O2 concentration had stabilized, the redox cycle was initiated. ii. Oxygen release and regeneration (CLOU) was tested in an N2 atmosphere for 300 s, or until the concentration of oxygen released dropped to 0. Specifically, the oxygen concentration was recorded together with the total amount of oxygen released and the conversion of the high entropy oxygen carrier (HEOC). During regeneration, it was determined whether the HEOC was able to capture all of the previously released oxygen and how much time this required at each temperature. iii. After the oxygen release and regeneration cycles, redox reactivity experiments were performed at 950 °C using syngas (50 vol% H2 and 50 vol% CO) as the reactant. During the redox cycles the stream initially consisted of inert gas (120 s) followed by syngas (10-20 s) and inert gas (120 s) before finally being oxidized in an air and N2 mixture (until complete regeneration). The regeneration and oxidation was carried out in the same way as in the CLOU cycles. During these experiments, the reactivity of the OC in the presence of syngas and its capacity for converting syngas to CO2 and H2O were analyzed. iv. The ability of the HEOC to release oxygen and regenerate was retested after the syngas experiments. For this purpose, the experiments shown in point i were performed again and the results obtained before and after syngas combustion were compared. To a achieve fast cooling of the bed the furnace was opened at the end of the last cycle, which led to a cool down from 950 °C to 500 °C at a rate of 90 °C/min. The gas used to fluidize the bed during the cooling period is the same as in the previous oxidation step.-- 2. HEOC Reactivity in TGA and Batch Fluidized Bed Reactor: 2.1 TGA reactivity. As can be seen from Figure S1, the oxidation, after reduction with either H2 or CLOU, shows a two step behavior in the reactivity, with one very fast initial step followed by a slower step, that cannot be attributed to different redox reactions. Even so, the OC conversion was complete for both redox reactions and the reactivity was maintained during the redox cycles. The CH4 reactivity was measured at 800 °C by reduction with a gas mixture containing 15 % CH4 and 20 % H2O. The reduction reactivity (Figure S2a) increased in a single step and reached the same value independent of the calcination temperature. The oxidation was complete and fast (see Figure S2b) and the OC conversion was maintained over the redox cycles. Still, the reactivities with CH4 were not remarkable compared to other OCs 18.-- 3. HEOC characterization: 3.1 SEM-EDX Figure S7 shows SEM images and EDX mappings of the fresh HEOC_1100 (Figure 13a,b,c) as well as oxidized particles from the batch fluidized bed after 30h of operation and a cool down from 950 °C, at a rate of 90 °C/min (Figure S7d,e,f). It is apparent that the particles do not show any shape modifications after use in the batch fluidized bed reactor. In addition, a homogeneous distribution of the five elements can, in general, be observed inside the particles. However, there are subdomains enriched in Mg (red zones in Figure S7c,f), which are more frequent in the fresh particles.-- Under a Creative Commons license CC BY NC ND 4.0., 1. Batch fluidized bed methodology. 2. HEOC Reactivity in TGA and Batch Fluidized Bed Reactor: 2.1 TGA reactivity. 2.2 Batch fluidized bed reactivity. Syngas combustion cycles. 3. HEOC characterization: 3.1 SEM-EDX. Mg-enriched subdomains, This work was partiatially funded by the Swedish Research Council (2020–03487) and the Gobierno de Aragón – Dpto. de Ciencia, Universidad y Sociedad del Conocimiento - Project LMP166_21. I. Adánez-Rubio acknowledges for “Juan de la Cierva” Program (Grant IJC2019-038987-I funded by MCIN/AEI/10.13039/501100011033) and for the “José Castillejo” international mobility program for young researchers (CAS21/00200)., Peer reviewed

-Table A1. Compounds analysed by chemical group, including precursor ion, two main fragmented ions, collision energy (CE) and polarity. -Table A2. Quality control of the analytical method including recovery of the different pharmaceuticals (n = 7 days) at different levels performed in pig liver (31, 63 and 125 ng/g) everyday samples of domestic animal carcasses were processed and analysed, including limit of detection (LOD) and quantification (LOQ) of the analytical technique, and R2 of matrix-matched calibration curves of each compound made in pig liver. -Table A3. Quality control of the analytical method including recovery of the different pharmaceuticals (n = 3 days) at different levels performed in chicken liver (31, 63 and 125 ng/g) everyday samples of avian scavenger tissues were processed and analysed, including limit of detection (LOD) and quantification (LOQ) of the analytical technique, and R2 of matrix-matched calibration curves of each compound made in chicken liver. -Table A4. Quality control of the analytical method including recovery of the different pharmaceuticals and caffeine (n = 1 days) at different levels performed in partridge plasma (18, 39 and 75 ng/mL) everyday samples of avian scavenger plasma samples were processed and analysed, including limit of detection (LOD) and quantification (LOQ) of the analytical technique, and R2 of matrix-matched calibration curves of each compound made in partridge plasma. -Table A5. Veterinary pharmaceutical concentrations detected in domestic animal carcasses by species and tissues supplied at supplementary feeding stations for vultures in Aragon, including average (± SD) and maximum levels (ng/g). -Table A6. Veterinary pharmaceutical and caffeine concentrations detected in positive samples in plasma from avian scavengers captured in Aragon and nearby regions, including average (± SD), minimum and maximum levels (ng/mL). -Fig. A1. Map showing the points where avian scavengers were captured, supplementary feeding stations are shown in black and landfills in orange., Peer reviewed

Fig S1. Location and situation of the carcass of the bearded vulture near a high voltage powerline. Author: José Carlos González Ruiz., Peer reviewed

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22 files, Data for the article Identifying Natural Bioactive Peptides from the Common Octopus (Octopus vulgaris Cuvier, 1797) Skin Mucus By-Products Using Proteogenomic Analysis, https://doi.org/10.3390/ijms24087145, No

Data acquisition: Satellite ESA SMOS mission (Soil Moisture and Ocean Salinity). Filenames: BEC_SSS___SMOS__ARC_L3__B_YYYYMMDDT120000_0.25km_9d_REP_v400.nc YYYYMMDD: central date. BEC ftp service: We serve netCDF data by means of a secure FTP server. NetCDF files from which the maps were made (and other additional data) can be downloaded from SFTP address becftp.icm.csic.es at port 27500. If your browser is SFTP compatible you can browse directly from sftp://becftp.icm.csic.es:27500 address. In order to download data you should be registered in our BEC FTP service. Registration is free, you can register by filling the following form: http://bec.icm.csic.es/bec-ftp-service-registration/ If you need a dedicated FTP client (for instance FileZilla https://filezilla-project.org/) you should use the following configuration: Host: sftp://becftp.icm.csic.es. Username: your username. Password: your password. Port: 27500, Dedicated regional Sea Surface Salinity (SSS) product in the Arctic Ocean. Level 3 9-day maps. Data acquisition: Satellite ESA SMOS mission (Soil Moisture and Ocean Salinity). Time coverage 01 February 2011 - 31 December 2023. Time resolution: 9-day. Maps frequency generation: Daily. Spatial coverage: Latitude range: 45ºN-90ºN Longitude range: 180ºW-180ºE. Spatial resolution: 25 kilometers. Spatial grid: EASE-Grid 2.0 Northern Hemisphere, Lambert Azimuthal (EPSG: 6931). Sensor Satellite SMOS / MIRAS. Format NetCDF. Climate and Forecast (CF) conventions version: 1.6, With the institutional support of the ‘Severo Ochoa Centre of Excellence’ accreditation (CEX2019-000928-S), Peer reviewed

Template_experimental contains the experimental warming and POC and MAOC data in cold vs other biomes .-- Template_observational contains the observational POC and MAOC data across cold regions., Peer reviewed

This repository may be useful for further studies, for the development of new therapeutic treatments for food intoxication and for tracking microbial sources in foodstuffs, Biogenic amine-producing bacteria are responsible for the production of basic nitrogenous compounds, such as histamine, cadaverine, tyramine and putrescine, after foods spoil due to microorganisms. In the present work, we applied a shotgun proteomics approach to quickly and easily characterize 15 different foodborne strains of biogenic amine-producing bacteria. A total of 10673 peptide spectrum matches (PSMs) belonging to 4081 nonredundant peptides and corresponding to 1811 annotated proteins were identified. With the results, relevant functional pathways were determined and the strains were differentiated into different Euclidean hierarchical clusters. Moreover, a predicted protein‒protein interaction network of biogenic amine foodborne strains was created. The whole confidence network contains 260 nodes and 1973 interactions. Most of the identified proteins were related to pathways and networks of energy, putrescine metabolism and host‒virus interaction. In addition, a total of 556 nonredundant peptides were identified as virulence factors, and most of these peptides corresponded to functions such as toxins, antimicrobial compound production, antimicrobial resistance, additional resistances and tolerances, host colonization and immune evasion, ABC transporters, phage proteins, and alternative virulence factors and proteins involved in horizontal transfer. Potential species-specific peptide biomarkers were screened. Thus, 77 species-specific peptide biomarkers belonging to 64 different proteins were proposed to identify 10 species (Enterobacter aerogenes, Enterobacter cloacae, Hafnia alvei, Klebsiella oxytoca, Morganella morganii, Proteus mirabilis, Proteus penneri, Proteus vulgaris, Raoutella planticola, Stenotrophomonas maltophilia). All of these results constitute the first major dataset of peptides and proteins of seafood biogenic amine-producing strains, Peer reviewed

Grant no. IT 1526-22 from the Basque Government for consolidated groups of the Basque University; Grants PID2019-107432GB-I00 and PID2022-139579NB-I00 both funded by MCIN/AEI/10.13039/501100011033 and by “ERDF A way of making Europe”; Spanish Ministry of Science and Innovation under the María de Maeztu Units of Excellence Program (CEX2020-001038-M/MCIN/AEI/10.13039/501100011033) and Grant PID2021-123949OB-I00 funded by MCIN/AEI/10.13039/501100011033 and by “ERDF A way of making Europe”; Swedish Research Council (VR, under grant No. 2020-04986). Swedish Research Council (VR, Research environment grant No. 2016-06059); Knut and Alice Wallenberg Foundation (KAW, under grant No. 2019.0140); Ministry of Science and Higher Education of the Russian Federation (Agreement No. 075-15-2021-606), Russian Science Foundation (grant No. 23-72-10005), and BASIS Foundation (grant No. 22-1-3-2-1). Work performed in part at the Chalmers Material Analysis Laboratory (CMAL), Peer reviewed

The dataset consists of comprehensive information on litter mass loss, elemental recycling (specifically nitrogen and phosphorus release rates), and associated environmental factors. The data was collected using standardized methods and includes details such as study location coordinates, climatic conditions (temperature and precipitation), ecosystem types (terrestrial and aquatic), study subjects (species identity), litterbag specifics (exclusion method and mesh size), and litter tissue types (woody and non-woody). Missing climatic data were obtained from the WorldClim database. The dataset comprises 1568 sets of pairwise comparisons, with 1060 for plant decomposition, 360 for nitrogen release, and 148 for phosphorus release. This comprehensive dataset serves as a valuable resource for studying litter decomposition, nutrient cycling, and the interplay between environmental factors and decomposition processes., Peer reviewed