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Fig. 8 Haplotype network for 44 in New insights into the phylogeny and taxonomy of Chinese species of Gagea (Liliaceae)-speciation through hybridization
Fig. 8 Haplotype network for 44 cpDNA haplotypes (psbA-trnH IGS+trnL-trnF IGS) including 38 sequences of representatives of Gagea sect. Gagea: G. aipetriensis (aip), G. ancestralis, G. angelae (ang), G. artemczukii (art), G. capusii (cap), G. erubescens (eru), G. helenae (hel), G. huochengensis (huo), G. lutea (lut), G. nakaiana (nak), G. paczoskii (pac), G. podolica (pod), G. pomeranica (pom), G. pratensis (pra), G. pusilla (pus), G. rubicunda (rub), G. shmakoviana (shm), G. terraccianoana (ter), G. tisoniana (tis), G.
Fig. 3 in Intermediary floral traits between natural hybrid and its parents in the XIquEXIquE (Cactaceae)
Fig. 3 Characterization of clad- odes and flowers of the hybrid and its parents in Catimbau National Park, Pernambuco, Brazil. Left, Xiquexique gounellei: cladode (A), lateral (B) and frontal (C) views of flower. In the middle, X.× heptagonus: cladode (D), side (E) and frontal (F) view of the flower of hybrid. Right, X. tuberculatus: cladode (G), side view (H) and front (I) of the flower of (Bar scale= 1 cm)
Fig. 6 in Intermediary floral traits between natural hybrid and its parents in the XIquEXIquE (Cactaceae)
Fig. 6 Comparison of colour spectra between the hybrid and its parents based on Euclidean distance plotted in a non-metric multidimensional scaling (NMDS)
Fig. 5 in Intermediary floral traits between natural hybrid and its parents in the XIquEXIquE (Cactaceae)
Fig. 5 Colour spectrum of flowers of the hybrid and its parents. In each of the spectra, the middle line indicates the mean reflectance and the shaded areas represent the standard deviation (SD). Reflectance spectrum of the external (EEP) and internal (IEP) elements of peri-
FIGURE 4 in Finding the last missing white oak hybrid from the Iberian Peninsula (Fagaceae, Quercus, sect. Quercus)
FIGURE 4. Abnormal leaf shapes of Q. ×gaonae, some with the proximal half of the leaf entire, as in Q. lusitanica and simultaneously with serrate margins, possessing deep lobes and divaricate secondary nerves, showing the influence of Q. canariensis, and indicating hybridization between these taxa.
FIGURE 2 in Finding the last missing white oak hybrid from the Iberian Peninsula (Fagaceae, Quercus, sect. Quercus)
FIGURE 2. Type location of Quercus ×gaonae (middle—red oval), developing conspicuously erect shoots, among the parents, the prostrate Q. lusitanica (left—turquoise oval) and growing below the Q. canariensis arboreal layer (above—green oval).
FIGURE 5 in Finding the last missing white oak hybrid from the Iberian Peninsula (Fagaceae, Quercus, sect. Quercus)
FIGURE 5. Indumentum details of Q. ×gaonae: 60×, 100× and 160×, yellowish fuzzy indumentum deriving from the parent Q. canariensis on the midrib and axillary veins; 200×, dominance of stellate and multistellate trichomes, deriving from the parent Q. lusitanica, on the abaxial leaf surface.
FIGURE 3 in Finding the last missing white oak hybrid from the Iberian Peninsula (Fagaceae, Quercus, sect. Quercus)
FIGURE 3. Holotype of Quercus ×gaonae Vila-Viçosa, Frias & F.M. Vázquez PO V72216! (Porto University, Natural History and Science Museum).
FIGURE 1 in Finding the last missing white oak hybrid from the Iberian Peninsula (Fagaceae, Quercus, sect. Quercus)
FIGURE 1. Location of the study area (Los Alcornocales Natural Park, in blue), in the Province of Cádiz and the location of the hybrid Quercus ×gaonae.
FIG. 5 in Comprehensive Analysis of Salamander Hybridization Suggests a Consistent Relationship between Genetic Distance and Reproductive Isolation across Tetrapods
FIG. 5. Genetic distances between salamanders that hybridize with heteromorphic sex chromosomes (median ¼ 0.109) and salamanders that hybridize without sex chromosomes (median ¼ 0.152). There is no significant difference (P ¼ 0.5293) between salamanders with sex chromosomes and salamanders without sex chromosomes.
FIG. 2 in Comprehensive Analysis of Salamander Hybridization Suggests a Consistent Relationship between Genetic Distance and Reproductive Isolation across Tetrapods
FIG. 2. (A) Histogram of cytochrome b (MT-CYB) genetic distance estimates (HKY85 þ C) between salamanders that hybridize. Graph bin width is 0.0125. (B) Ratio of mitochondrial MT-CYB genetic distance to nuclear recombination activating 1 (RAG1) genetic distance between parental species of salamanders that hybridize on a log scale. The ratio of genetic distance ranged from 0.6 to 162 with the majority of species pairs having a higher mitochondrial genetic distance (median ¼ 21.1).
FIG. 3. Cytochrome b in Comprehensive Analysis of Salamander Hybridization Suggests a Consistent Relationship between Genetic Distance and Reproductive Isolation across Tetrapods
FIG. 3. Cytochrome b (MT-CYB) genetic distances between parental species that hybridize in different tetrapod groups. Kruskal-Wallis H test showed no significant differences across the groups (P ¼ 0.661). Salamanders are not hybridizing across greater genetic distances.
FIG. 1 in Comprehensive Analysis of Salamander Hybridization Suggests a Consistent Relationship between Genetic Distance and Reproductive Isolation across Tetrapods
FIG. 1. Salamander hybrids are found in most families (Pyron and Wiens, 2011). About 12.1% of salamanders are known to hybridize with over half belonging to Plethodontidae. There was no significant correlation between the number of papers per species and the proportion of salamanders found to hybridize (Kendall's rank correlation P ¼ 0.236).
FIG. 4 in Comprehensive Analysis of Salamander Hybridization Suggests a Consistent Relationship between Genetic Distance and Reproductive Isolation across Tetrapods
FIG. 4. Genetic distance ratio of mitochondrial cytochrome b (MTCYB) to nuclear recombination activating 1 (RAG1) for pairs of species that hybridize in major tetrapod clade on a log scale. Kruskal-Wallis H test showed no strong significant differences across the four groups (P ¼ 0.108).
Figure 3 in Genetic data to describe the hybrid zone between Bufo bufo (Linnaeus, 1758) and Bufo verrucosissimus (Pallas, 1814) in northeastern Türkiye
Figure 3. Cline analysis of nuclear (based on STRUCTURE Q-scores) and mitochondrial data across the Bufo bufo/Bufo verrucosissimus (Common Toad/ Caucasian Toad) hybrid zone along a west-east transect. Each point represents one population and grey shades represent 95% confidence intervals of fitted clines.
Figure 2 in Genetic data to describe the hybrid zone between Bufo bufo (Linnaeus, 1758) and Bufo verrucosissimus (Pallas, 1814) in northeastern Türkiye
Figure 2. Interpolation map (a) and individual assignment barplot (b) constructed under K = 2 in Structure corresponding to the genetic pools of Bufo bufo (Common Toad) and Bufo verrucosissimus (Caucasian Toad). Different shadings show probabilities of belonging to the respective species (blue for Bufo bufo and yellow for Bufo verrucosissimus). Dark shades represent pure populations of each species whereas lighter shades indicate higher admixture. The white range indicates maximum admixture in the center of the hybrid zone.
Figure 1 in Genetic data to describe the hybrid zone between Bufo bufo (Linnaeus, 1758) and Bufo verrucosissimus (Pallas, 1814) in northeastern Türkiye
Figure 1. Admixture proportions of each population as illustrated by pie charts on the map of the study area (a) according to STRUCTURE results (b), with information on mtDNA haplotypes observed in each population displayed over the STRUCTURE barplot. The inset map, modified from Özdemir et al. (2020), represents the geographic range of the Bufo bufo species group, with arrows pinpointing the western hybrid zone between Bufo spinosus (Iberian Common Toad, in red) and Bufo bufo (Common Toad, in blue) and potential contact areas between Bufo bufo and Bufo verrucosissimus (Caucasian Toad, in yellow) in Türkiye. The scatterplots of PCA (c) and DAPC (d) represent three groups (Bb: Bufo bufo; Bv: Bufo verrucosissimus; Hybrid: YAY population). Green dashed lines: Rize borders; Ruby red dashed lines: Artvin borders; Cyan line: Çoruh River along Artvin.
Supplementary data for the article: "Towards an widely applicable earthquake detection algorithm for fibreoptic and hybrid fibreoptic-seismometer networks"
<p>Repository of supporting data associated with the article submitted to GJI, titled: "Towards an widely applicable earthquake detection algorithm for fibreoptic and hybrid fibreoptic-seismometer networks".</p> <p> </p> <p>Contents include:</p> <ol> <li>A full working example of modified QuakeMigrate version and seismic time-series data used to detect an earthquake.</li> <li>Earthquake catalogues for the three datasets described in the publication.</li> </ol>
Retrieved studies for Impacts of the Adoption of Hybrid Work on Collaboration in Information Technology Teams
<p>Retrieved studies for Impacts of the Adoption of Hybrid Work on Collaboration in Information Technology Teams</p>
Dataset for the article "A deep equivariant neural network approach for efficient hybrid density functional calculations"
<p>Dataset files for DeepH-hybrid, containing structures and preprocessed Hamiltonian matrices computed with HSE06 hybrid functional and ABACUS DFT package.</p> <p>Enclosed include:</p> <ol> <li>The four datasets corresponding to the four DeepH-hybrid models mentioned in DeepH-hybrid's paper, each containing material structures and electronic structure properties of </li> <li>Basis set files for the ABACUS DFT package</li> <li>Snapshot of a version of the additional codes utilized to preprocess hybrid DFT Hamiltonians (also available via this <a href="https://github.com/aaaashanghai/DeepH-hybrid">GitHub link</a>)</li> </ol> <p>Note only the additional codes of DeepH-hybrid is provided, and it may be used in combination with DeepH-E3 package for neural-network training. For additional details please refer to the "README" file of the code.</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.