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FIGURE 1 in A new glass sponge genus (Hexactinellida: Euplectellidae) from abyssal depth of the Yap Trench, northwestern Pacific Ocean
FIGURE 1. Rhizophyta yapensis gen. et sp. nov., specimens. A. Holotype. Whole specimen (A1), lateral view of atrial surface (A2), and half-lateral view of dermal surface (A3). B. Paratype A. Whole collected sample (B1) and in situ image (B2). C. Paratype B. Collected sample (C1), dermal surface (C2), and atrial surface (C3). D. Paratype C. Collected sample with main body cut in half (D1), lateral view of main body (D2), and dermal surface (D3).
FIGURE 2 in A new glass sponge genus (Hexactinellida: Euplectellidae) from abyssal depth of the Yap Trench, northwestern Pacific Ocean
FIGURE 2. Rhizophyta yapensis gen. et sp. nov., surfaces of holotype. A. Atrial surface. B. Close-up image of atrial lattice. C. SEM of atrial lattice. D. Dermal surface with radiating subdermal strands of diactins. E. Close-up image of dermal lattice. F. SEM of dermal lattice. G. Base of peduncle with root-like structures. H. Close-up image of the veil of pentactins covering the peduncle. I. SEM of the veil of pentactins covering the peduncle. J. SEM of fused diactins in root-like structures.
Data to "Distinguishing mirror from glass: A 'big data' approach to material perception"
<p>This record contains images, models, and analysis scripts written in MATLAB.</p> <p>Tamura, Prokott, Fleming. "Distinguishing mirror from glass: A ‘big data’ approach to material perception." in preparation.</p>
Iterative quantum optimization of spin glass problems with rapidly oscillating transverse fields
Open the record for dataset details and reuse information.
DFT datasets for training machine-learning potential to model Cl-doped lithium borosilicate glasses using DeePMD
<h2><strong>Li diffusion in oxygen-chlorine mixed anion borosilicate glasses using</strong></h2> <h2><strong>a machine-learning simulation</strong></h2> <h5>Shingo Urata, Noriyoshi Kayaba</h5> <ul> <li>DFT_Data_for_Cl-doped_LBSCl_glass.zip inlucudes atom configurations, energies, forces, box size, atom types, atom kinds, and virial in coord.raw, energy.raw, force.raw, type.raw, type_map.raw, and virial.raw, respectively. </li> <li>All DFT data were evaluated using PBE with a cutoff energy of 600 eV by VASP.</li> <li>The other detasets are available from https://doi.org/10.5281/zenodo.10577559</li> <li>LBSCl_DMD_model.pb is force field developed using DeePMD-kit.</li> <li>LBSCl_DMD_model_c.pb.zip is the compressed version of LBSCl_DMD_model.pb.</li> </ul>
Adhesion of silicate impact melts on impact glasses of Chang'e-5 regolith
<p><span>Reference data of components in Chang'e-5 regolith, and geochemical data gathered for five studied Chang'e-5 impact glass particles and surface microscopic silicate melts.</span></p>
Data and code of "Unified percolation scenario for the α and β processes in simple glass formers
<p>Molecular dynamics simulation data and post-processing code for "Unified percolation scenario for the α and β processes in simple glass formers"</p>
Figure 6 in Reproductive behaviour of the glass frog Hyalinobatrachium cappellei (Anura: Centrolenidae) in the Southern Amazon
Figure 6. Observed predation and parasitoid events on Hyalinobatrachium cappellei clutches in Cotriguaçu, Mato Grosso, Brazil. Clutches without male attendance suffering predation by (a) Blattodea; (b) Noctuidae moth family; (c) Tettigoniidae bush crickets; and (d) ants, Pheidole sp. (e, f) Abandoned clutch, process of dehydration and initiated fungi development after four days.
Figure 5 in Reproductive behaviour of the glass frog Hyalinobatrachium cappellei (Anura: Centrolenidae) in the Southern Amazon
Figure 5. First two axes of nonmetric multidimensional scaling (NMDS), composed by acoustics parameters of advertisement call (A) and courtship call (C) of Hyalinobatrachium cappellei in Cotriguaçu, Mato Grosso, Brazil.
Figure 3 in Reproductive behaviour of the glass frog Hyalinobatrachium cappellei (Anura: Centrolenidae) in the Southern Amazon
Figure 3. Non-aggressive behaviours of Hyalinobatrachium cappellei in Cotriguaçu, Mato Grosso, Brazil. (a) Two males vocalizing on different leaves of the same plant; (b) two males sharing the same leaf, the arrow indicates couple in amplexus; (c) invasive couple in amplexus, with the arrow indicating the male resident; (d) female retreating from a couple in amplexus.
Figure 1 in Reproductive behaviour of the glass frog Hyalinobatrachium cappellei (Anura: Centrolenidae) in the Southern Amazon
Figure 1. Reproductive behaviours of Hyalinobatrachium cappellei at Cotriguaçu, Mato Grosso, Brazil. (a) Vocalizing male on the upper face of leaf with a clutch on the lower face; (b) clutch with hatching tadpoles; (c) multiple disposition of clutches on the same leaf; (d) male ventral brooding behaviour after remaining for a few minutes in the rain; (e) male near clutch during the day; (f) couple in amplexus.
Figure 2 in Reproductive behaviour of the glass frog Hyalinobatrachium cappellei (Anura: Centrolenidae) in the Southern Amazon
Figure 2. Sequence of courtship and oviposition behaviour in Hyalinobatrachium cappellei (a, b) Female approaching the calling male which initiates the vocalization of courtship call; (c) female touching the male; (d) male 'turns' its body around the female; (e) amplexus formation; (f) couple traverses both the upper and lower face of the leaf; (g) oviposition, (h) female leaves the top of clutch while male remains, rotating the body; (i) male remains on clutch while the female abandons the reproductive site. Illustration by Milton Cordova.
Figure 7 in Reproductive behaviour of the glass frog Hyalinobatrachium cappellei (Anura: Centrolenidae) in the Southern Amazon
Figure 7. Number of clutches recorded in a 10-day period between Hyalinobatrachium cappellei males initially with clutches and males initially without clutches at Cotriguaçu, Mato Grosso, Brazil.
Figure 4 in Reproductive behaviour of the glass frog Hyalinobatrachium cappellei (Anura: Centrolenidae) in the Southern Amazon
Figure 4. Sonogram and oscillogram of (a) advertisement call and (b) courtship call of Hyalinobatrachium cappellei at Cotriguaçu, Mato Grosso, Brazil.
Figure 7 in Reproductive ecology of the glass frog Espadarana prosoblepon (Anura: Centrolenidae) in an urban forest of the Central Andes of Colombia
Figure 7. Preferred use of fronds of Selaginella geniculata as substrates for oviposition in Espadarana prosoblepon in a population in the Botanical Garden at Universidad del Quindío, Armenia, Colombia. The expected legend refers to the number of clutches that should be found in a given substrate category according to the abundance of these in the habitat; the observed legend refers to the actual number of clutches found per substrate category in this study. The category 'Leaves' refers to leaves of species other than S. geniculata while 'Others' refers to branches, trunks, and rocks.
Figure 6 in Reproductive ecology of the glass frog Espadarana prosoblepon (Anura: Centrolenidae) in an urban forest of the Central Andes of Colombia
Figure 6. (a) Amplexus, (b) oviposition, (c) abandonment of the oviposition site by the male and (d) egg attendance by the female in Espadarana prosoblepon.
Figure 5 in Reproductive ecology of the glass frog Espadarana prosoblepon (Anura: Centrolenidae) in an urban forest of the Central Andes of Colombia
Figure 5. (a) Relationship between the body size of males, and chorus tenure (i.e. number of nights a same male was recorded over the duration of the study or until was recorded in amplexus). (b) Influence of chorus tenure in males and their probability of mating. (c) Lack of assortative mating by body size of individuals in amplexus. (d) Relationship between the body size of the females and the size of their egg clutches. Regression line is showed only for the statistically significant tendency at α = 0.05.
Figure 4 in Reproductive ecology of the glass frog Espadarana prosoblepon (Anura: Centrolenidae) in an urban forest of the Central Andes of Colombia
Figure 4. Variation of (a) rainfall and environmental temperature; (b) number of males and females; and (c) egg clutches in the study area between December 2013 and November 2015. Extensions of the bars in the middle figure indicate standard deviation.
Figure 3 in Reproductive ecology of the glass frog Espadarana prosoblepon (Anura: Centrolenidae) in an urban forest of the Central Andes of Colombia
Figure 3. Frequency of activity (number of nights a same individual was observed) of males (left plot) and females (right plot) of the glass frog Espadarana prosoblepon between December 2013 and November 2015 in the Botanical Garden at Universidad del Quindío, Armenia, Central Andes of Colombia.
Figure 2 in Reproductive ecology of the glass frog Espadarana prosoblepon (Anura: Centrolenidae) in an urban forest of the Central Andes of Colombia
Figure 2. Example of patterns of black and yellow dots observed on the back of adult individuals of Espadarana prosoblepon and used to monitor males and females.
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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.