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Fig. 1. A in Scientific Note Does the association of young fishes with jellyfishes protect from predation? A report on a failure case due to damage to the jellyfish
Fig. 1. A watchful comb grouper (Mycteroperca acutirostris) while following the jellyfish (Chrysaora lactea) tries to approach a small group of juvenile scads (Trachurus lathami), and induce them to leave the shelter on the top and among the tentacles of the jellyfish.
Fig. 2 in Scientific Note Does the association of young fishes with jellyfishes protect from predation? A report on a failure case due to damage to the jellyfish
Fig. 2. Juvenile carangids and other fishes tend to stay close to a jellyfish's umbrella or among its tentacles while frightened.
Figure 10 in The skull of Yunnanosaurus huangi Young, 1942 (Dinosauria: Prosauropoda) from the Lower Lufeng Formation (Lower Jurassic) of Yunnan, China
Figure 10. The single most parsimonious tree found by the analysis of the modified Galton & Upchurch (2004) data matrix. Material included as 'Sellosaurus' is currently regarded as Efraasia (Yates, 2003b); specimens included as 'Euskelosaurus' are currently referred to Plateosauravus cullingworthi (Yates, 2003c).
Figure 9 in The skull of Yunnanosaurus huangi Young, 1942 (Dinosauria: Prosauropoda) from the Lower Lufeng Formation (Lower Jurassic) of Yunnan, China
Figure 9. The single most parsimonious tree produced by analysis of the modified Yates (2003a) data matrix. For the sake of brevity, species of Thecodontosaurus are listed using the abbreviation of the generic name. The material included as 'Euskelosaurus' is currently referred to Plateosauravus cullingworthi (Yates, 2003c).
Figure 8. A, a in The skull of Yunnanosaurus huangi Young, 1942 (Dinosauria: Prosauropoda) from the Lower Lufeng Formation (Lower Jurassic) of Yunnan, China
Figure 8. A, a strict consensus tree of the 124 most parsimonious trees found by the analysis of the modified version of Sereno's (1999) data matrix. B, a 50% majority-rule consensus tree based on the 12 reduced consensus topologies produced by re-analysis of the modified Sereno (1999) data matrix. 'Gripposaurus' represents a referred individual of 'Gyposaurus' sinensis (Young, 1948); material included as 'Sellosaurus' is currently regarded as Efraasia (Yates, 2003b).
Figure 6 in The skull of Yunnanosaurus huangi Young, 1942 (Dinosauria: Prosauropoda) from the Lower Lufeng Formation (Lower Jurassic) of Yunnan, China
Figure 6. Skull and atlas-axis complex of Yunnanosaurus huangi (NGMJ 004546) in occipital view. A, drawing of skull as preserved. B, interpretative line drawing of the skull showing damaged areas, reconstruction, and areas obscured by matrix. See Appendix 2 for abbreviations.
Figure 4 in The skull of Yunnanosaurus huangi Young, 1942 (Dinosauria: Prosauropoda) from the Lower Lufeng Formation (Lower Jurassic) of Yunnan, China
Figure 4. Skull and atlas-axis complex of Yunnanosaurus huangi (NGMJ 004546) in dorsal view. A, drawing of skull as preserved. B, interpretative line drawing of the skull showing damaged areas, reconstruction, and areas obscured by matrix. See Appendix 2 for abbreviations.
Figure 5 in The skull of Yunnanosaurus huangi Young, 1942 (Dinosauria: Prosauropoda) from the Lower Lufeng Formation (Lower Jurassic) of Yunnan, China
Figure 5. Skull roof of Yunnanosaurus huangi (NGMJ 004546) in dorsal view showing frontal and parietal bosses (arrowed). Scale bar equals 30 mm. The cranial end of the snout is to the right. See Appendix 2 for abbreviations.
Figure 2 in The skull of Yunnanosaurus huangi Young, 1942 (Dinosauria: Prosauropoda) from the Lower Lufeng Formation (Lower Jurassic) of Yunnan, China
Figure 2. Skull and atlas-axis complex of Yunnanosaurus huangi (NGMJ 004546) in right lateral view. A, drawing of skull as preserved. B, interpretative line drawing of the skull showing damaged areas, reconstruction, and areas obscured by matrix. See Appendix 2 for abbreviations.
Figure 1 in The skull of Yunnanosaurus huangi Young, 1942 (Dinosauria: Prosauropoda) from the Lower Lufeng Formation (Lower Jurassic) of Yunnan, China
Figure 1. Skull and atlas-axis complex of Yunnanosaurus huangi (NGMJ 004546). A, right lateral view. B, left lateral view. C, dorsal view. Scale bar equals 100 mm.
KU Car, a young massive eclipsing binary system in NGC 3324
<p>Massive stars are needed engines in the galactic clockwork for the chemical evolution of the Galaxy and the energetic input to the ISM. These stars suffer endemic multiplicity, and thus, studies of the origin and evolution of massive stars is tied to the study of binaries. Therefore, eclipsing binary systems are indispensable objects because absolute parameters (e.g. masses, radii, etc.) can be derived combining the study and modeling of radial velocity and light curves. Such absolute parameters derived from direct observations help to test models about the structure and evolution of massive stars. In this talk, we are presenting an analysis of the light and radial velocity curves of the eclipsing binary system KU Car (P=2.96 d). This binary, composed by a B0.5-0.7 V primary and an unseen companion, shows a remarkable light-curve with a sharp and deep primary minimum and a shallow secondary minimum with strong "reflection effect". Using PHOEBE 2.1 code for modeling, we have derived absolute parameters for both stars proposed the evolutionary stage. This Algol-like system dominated by a young early-B type star, is located in the center of NGC 3324, a bubble-like star-forming region also known as "Gabriela Mistral" Nebula. The photometric analysis is based on multi-band observations obtained using LCOGTN telescopes, and data gathered from ASAS-3, ASAS-SN, TESS, and GDS projects spanning a period of about 18 years. Radial velocities were determined using spectroscopic observations obtained at LCO/duPont and ESO-LSO/2p2 telescopes in the framework of "OWN Survey" and "B-SUGOS" projects.</p>
Figure 5 in Old lake versus young taxa: a comparative phylogeographic perspective on the evolution of Caspian Sea gastropods (Neritidae: Theodoxus )
Figure 5. EBSPs indicating population trends for the pooled Pontocaspian (blue) and southern Iranian (red) Theodoxus groups. The central line of each plot represents the median value and the shaded area indicates the 95% confidence interval. Note the EBSPs depict marginally different starting dates for each group when compared with the phylogeny. Importantly, however, there is a strong overlap of EBSP starting dates with the 95% HPDs established for the onset of intraspecific diversification in each group, as shown in the phylogeny (figure 3).
Figure 1 in Old lake versus young taxa: a comparative phylogeographic perspective on the evolution of Caspian Sea gastropods (Neritidae: Theodoxus )
Figure 1. Representative phenotypes of the Pontocaspian and southern Iranian Theodoxus species studied herein. Pontocaspian: (a,b) T. pallasi (UGSB 20712); (c,d) T. astrachanicus (UGSB 18130); (e,f) T. pallasi (UGSB 18091); (g,h) T. major (UGSB 20482); (i,j) T. major (UGSB 20496); (k,l) T. schultzii (UGSB 20791). Southern Iranian: (m,n) T. doriae (UGSB 21706); (o,p) T. pallidus (UGSB 22228). Scale bar, 1 mm.
Figure 4. Statistical haplotype networks for COI, 16S in Old lake versus young taxa: a comparative phylogeographic perspective on the evolution of Caspian Sea gastropods (Neritidae: Theodoxus )
Figure 4. Statistical haplotype networks for COI, 16S and ATPα sequence data for Pontocaspian and southern Iranian Theodoxus groups. The total number of sequences in each network is demarcated by 'n'. The circle sizes represent the relative frequency of sequences per haplotype. The number of site changes separating haplotypes is indicated by blank dots. Colours correspond to the sampling locations, as indicated in the key and in figure 2. Haplotype groupings are boxed and labelled according to the phylogroups determined through the dated phylogeny (I–VI; figure 3).
Figure 2 in Old lake versus young taxa: a comparative phylogeographic perspective on the evolution of Caspian Sea gastropods (Neritidae: Theodoxus )
Figure 2. Map depictingthelocationsof thesamplingsitesaround the Pontocaspiansystemandsouthern Iran. Coloursof dots correspond to the locations, as indicated in the key. Dashed lines encircle (I) the Pontocaspian and (II) the southern Iranian Theodoxus sampling localities. The size of the dots represents the sample size at each location (larger = 10 specimens; smaller = 5 specimens).
Figure 3 in Old lake versus young taxa: a comparative phylogeographic perspective on the evolution of Caspian Sea gastropods (Neritidae: Theodoxus )
Figure 3. Dated phylogeny of Pontocaspian and southern Iranian Theodoxus spp. constructed in BEAST based on COI, 16S and ATPα sequence data. Supported phylogroups of Pontocaspian and southern Iranian Theodoxus are labelled Ito VI. Node labels among these phylogroups and outgroup species denote divergence time in millions of years ago (Ma), with the 95% credibility interval given in parentheses and as grey bars for in-group taxa. Small red squares at nodes (with darkened node bars and, in some instances, dates) indicate significant posterior probabilities of divergence events. Parallel to each supported phylogroup, coloured bars indicate the localities and respective morphospecies of the included specimens as defined in the key on the left. Caspian Sea lake-level variations over the last 1.5 million years (relative to absolute sea level) and regional stratigraphy (following the 'short–Akchagylian' option) are adapted from Krijgsman et al. [1] (Khv., Khvalynian).
Reproduction Package for the paper "The early evolution of young massive clusters. The kinematic history of NGC6611 / M16"
<p>This is a comprehensive reproduction package for the paper "The early evolution of young massive clusters. The kinematic history of NGC6611 / M16" by <a href="https://ui.adsabs.harvard.edu/abs/2022arXiv220708452S/abstract">Stoop et al. (2022)</a>.</p> <p>This reproduction package aims for open science, with the internal API designation of 'Gold'.</p> <p>This package aims to provide the raw data, and the software and scripts to produce the intermediate and end products. Software and scripts are also available to produce the figures and tables in the paper.</p> <p> </p>
Data for: Determining Young's modulus of arbitrarily-shaped granite samples using accurate grain-based modelling with Micro-RME
<p>HaH 346 meteorite samples with shock melt veins are tested using the nanoindentation experiment with Berkovich indenter. The data includes Young's modulus of different rock-forming minerals measured by nanoindentation test and Raman spectrum data for jadeite and wadsleyite in HaH346 meteorite. </p>
Dataset of the visual EEG oddball paradigm with young and older age group
<p>The data accompanies the research described in yet unpublished paper: "On the influence of aging on classification performance in the visual EEG oddball paradigm using statistical and temporal features" by Omejc, N., Peskar, M., Miladinović, A., Kavcic, V., Džeroski, S., Marusic, U.</p> <p>The package includes raw data, that were measured by 32-channel EEG set and stored as hpf5 file, preprocessed data. that were preprocessed using custom scripts that utilize EEGLAB and its plugins, and data that was at the end used in the classification task and includes two types of datasets, one with temporal features and another with ERP statistical features, as in more detail described in the paper. Additionally, the package includes locations of 32 channels on the head, the event mappings for both the older and the younger group, as well as some general information about the subjects.</p>
Data and R code from: Haemosporidian infections influence risk-taking behaviours in young male blackcaps Sylvia atricapilla
<p>This repository contains all data and code necessary to reproduce the results and figures of the paper:</p> <p>Remacha, C., Ramírez, A., Arriero, E. and Pérez-Tris, J. 2023. Haemosporidian infections influence risk-taking behaviours in young male blackcaps <em>Sylvia atricapilla</em>. Animal Behaviour, 196, 113-126. <a href="https://doi.org/10.1016/j.anbehav.2022.12.001">https://doi.org/10.1016/j.anbehav.2022.12.001</a></p> <p>The repository contains a readme file (README_SYAT_MS_ANIBEH_Scripts.txt) with a description of the code and the data. The code is organised in eight R script files. Instructions to run the code are provided in the readme file. The data are organised in two separate files. One file (SYAT_MS_BH_ANIBEHdata.txt) contains data of exploratory and antipredatory behaviours of 43 young male blackcaps. The other one (SYAT_MS_BH_BIOL_ANIBEHdata.txt) contains biological and experimental attributes of the same individuals: status and intensity of parasite infection, experimental treatment, morphology and body mass.</p>
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.