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The digital text of the 13 books of the "Confessiones" by Augustinus is taken from The Latin Library (http://www.thelatinlibrary.com/august.html). The original text was lemmatized and PoS tagged with the UDPipe tool (using the PROIEL trained model). The output of UDPipe was then checked manually at the CIRCSE Research Centre of the Università Cattolica del Sacro Cuore, Milan, Italy. The linking of the text to the Lemma Bank of the LiLa Knowledge Base was performed at CIRCSE, too.

Supplemental material, supplementary_material for Climate variability of the last ~2700 years in the Southern Adriatic Sea: Coccolithophore evidences by Antonio Cascella, Sergio Bonomo, Bassem Jalali, Marie-Alexandrine Sicre, Nicola Pelosi, Sabine Schmidt and Fabrizio Lirer in The Holocene

This dataset contains the dissolved organic matter (DOM) quantification and optical characterisation results from a KOSMOS mesocosm experiment carried out in the framework of the Ocean Artificial Upwelling project. The experiment was carried out in the autumn of 2018 in the oligotrophic waters of Gran Canaria. During the 39 days of experiment nutrient-rich deep water was added to the mesocosms in two modes (singular vs recurring additions), with four levels of intensity. Dissolved organic carbon, nitrogen and phosphorus were quantified with a Shimadzu TOC-5000 and a QuAAtro AutoAnalyzer. The absorption and fluorescence proprieties of DOM were determined making use of an Ocean Optics USB2000+UV-VIS-ES Spectrometer and a Jobin Yvon Horiba Fluoromax-4 spectrofluorometer, respectively. The aim of this dataset was to study the effect of artificial upwelling on the dissolved organic matter pool and its potential implications for carbon sequestration.

ELMo language model (https://github.com/allenai/bilm-tf) used to produce contextual word embeddings, trained on entire Gigafida 2.0 corpus (https://viri.cjvt.si/gigafida/System/Impressum) for 10 epochs. 1,364,064 most common tokens were provided as vocabulary during the training. The model can also infer OOV words, since the neural network input is on the character level.

In this dataset, we present Fe, Na and Ca concentration and fluxes retrieved from the North Greenland Eemian Ice Drilling (NEEM) ice core project, covering the last 108 kyrs. The sampling resolution was 110 cm. To ensure an effective dissolution of Fe particles, samples were acidified to pH 1 using Suprapure nitric acid and stored at room temperature for 1 month before the analysis. The ice samples were analyzed with an Inductively Coupled Plasma Single Quadrupole Mass Spectrometer equipped with a quartz Scott spray chamber. Limits of Detection, calculated as three times the standard deviation of the blanks, were 0.8 µg L-1 for 57Fe, 1 µg L-1 for Ca and 3 µg L-1 for Na. Our results show that Holocene Fe fluxes (0.042 -11.7 kyr b2k, 0.5 mg m-2 yr-1) at the NEEM site were four times lower than the average recorded over the last glacial period (11.7– 108 kyr b2k, 2.0 mg m-2 yr-1), while they were greater during the Last Glacial Maximum (LGM, 14.5 – 26.5 kyr b2k, 3.6 mg m-2 yr-1) and Marine Isotope Stage 4 (MIS 4, 60 - 71 kyr b2k, 5.8 mg m-2 yr-1). We present Fe, Ca and Na concentration and fluxes. Dating (GICC05modelext-NEEM-1) and accumulation data are from Rasmussen et al., 2013.

The IBM 3D models and derivative products were generated via a typical Image-based modeling pipeline. The aerial photos were collected by the UC Merced team using a DJI Phantom 3 Pro multi-rotor drone. The geospatial control data was collected by California State Parks licensed surveyor David Gutierrez using a Trimble differential GPS and Trimble robotic total station. The TLS LiDAR data were collected by the UC Merced team using a FARO Focus 3D S120 range finder and processed in FARO Scene and CloudCompare. The CAD drawings were created by Arianna Campiani using orthographic views of the buildings' terrestrial laser scanning point clouds produced by Scott McAvoy in the Potree Viewer. Dataset includes all the natively digital geospatial and 3D data collected in our topographic and 3D survey of the iconic Dechambeau Hotel & IOOF Hall buildings located at the entrance of town on Main St.

This dataset contains environmental data (temperature, relative humidity, and, in some cases, light and ultraviolet radiation levels) of partner museums of the European Horizon 2020 CollectionCare project . The following museums provided data to create this compilation and consolidation: Alava Arms Museum (Spain), Alava Fine Arts Museum (Spain), National Historical Museum (Greece), The Ethnographic Open Air Museum of Latvia, The Royal Danish Collection - Rosenborg (Denmark).

Additional file 3: Table S1. Genes located within consensus homozygous segments in Exmoor ponies.

This table contains the quantities of each pottery class at each site identified during archaeological surveys in Vidarbha, Maharashtra, India. The data is arranged according to the archaeological sites. For each site, the number of sherds and the MNI count are presented.

We freeze-dried and homogenized 44 samples of c. 0.7-1.8 g dry sediment from core PG1351 covering late glacials and interglacials of MIS 8 to MIS 5e, integrating sediment of 1 cm core depth. Temporal resolution of these samples ranges from 140 to 960 years per sample. For the period between 430 and 405 kyrs ago (end of MIS 12 to MIS 11c), 13 samples of 0.5-1.3 g of dry sediment from ICDP core 5011-1 were taken for MA analyses, integrating sediment of 2 cm core depth. Eight of these 13 samples are from the same core depths as were previously analysed for pollen (Melles et al., 2012). Temporal resolution of these samples varies between 200 and 970 years per sample comparable to core PG1351. Across all samples, temporal resolution is 333 ± 273 years per sample, giving centennial- to millennial scale averages. We extracted the polar lipids of all MA samples using a Dionex Accelerated Solvent Extraction system (ASE 350, ThermoFisher Scientific) at 100°C, 103 bar pressure and two extraction cycles (20 min static time) with 100 % methanol, after an ASE cycle with 100 % dichloromethane. For every sample sequence (n=13-18), we extracted a blank ASE cell and included it in all further steps. We added 60 ng of deuterated levoglucosan (C6H3D7O5; dLVG; Th. Geyer GmbH & Co. KG) as internal standard, and filtered the extract over a PTFE filter using acetonitrile and 5 % HPLC-grade water. We analysed the extracts with an Ultimate 3000 RS ultra-high performance liquid chromatograph (U-HPLC) with thermostated autosampler and column oven coupled to a Q Exactive Plus Orbitrap mass spectrometer (Quadrupole-Orbitrap MS; ThermoFisher Scientific) with heated electrospray injection (HESI) probe at GFZ Potsdam, using measurement conditions adapted from earlier studies (Hopmans et al., 2013;Schreuder et al., 2018;Dietze et al., 2019). Briefly, separation was achieved on two Xbridge BEH amide columns in series (2.1 x 150 mm, 3.5 um particle size) fitted with a 50 mm pre-column of the same material (Waters). The compounds were eluted (flow rate 0.2 mL min-1) with 100 % A for 15 minutes, followed by column cleaning with 100 % B for 15 min, and re-equilibration to starting conditions for 25 min. Eluent A was acetonitrile:water:triethylamine (92.5:7.5:0.01) and eluent B acetonitrile:water:triethylamine (70:30:0.01). HESI settings were as follows: sheath gas (N2) pressure 20 (arbitrary units), auxiliary gas (N2) pressure 3 (arbitrary units), auxiliary gas (N2) temperature of 50 ˚C, spray voltage -2.9 kV (negative ion mode), capillary temperature 300 °C, S-Lens 50 V. Detection was achieved by monitoring m/z 150-200 with a resolution of 280,000 ppm. Targeted data dependent MS2 (normalized collision energy 13 V) was performed on any signal within 10 ppm of m/z 161.0445 (calculated exact mass of deprotonated levoglucosan and its isomers) or m/z 168.0884 (calculated exact mass of deprotonated dLVG) with an isolation window of 0.4 m/z. The detection limit was 2.5 pg on column, based on injections of 0.5 to 5000 pg on column of authentic standards of LVG, MAN, and GAL (Santa Cruz Biotechnology) and dLVG. Integrations were performed on mass chromatograms within 3 ppm mass accuracy and corrected for relative response factors to dLVG (1.08 ± 0.10, 0.76 ± 0.10 and 0.24 ± 0.05 for LVG, MAN, and GAL, respectively), according to known authentic standard mixes injected before and after every measurement sequence and supported by characteristic isomer-specific MS² data. All samples were corrected by subtracting the maximum MA concentrations in the blank duplicates of each ASE sequence. To account for biases due to sediment properties and sedimentation rates, MA influxes (mass accumulation rates in ng cm-2 yr-1) were calculated by multiplying the concentrations (ng g-1) with the sample-specific dry bulk densities (Melles et al., 2007;Wennrich et al., 2016), and the sample's sedimentation rates (cm yr-1) using the age-depth models presented by Nowaczyk et al. (2013) for the the PG1351 and the ICDP-5011-1 cores.