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FIGURES 9a–d in Revision of the Old World species of the genus Tephritis (Diptera, Tephritidae) with a pair of isolated apical spots
FIGURES 9a–d. Tephritis dilacerata dilacerata: a—lectotype ♀ habitus; b–d—wings; bar = 1 mm.
FIGURE 32 in Revision of the Old World species of the genus Tephritis (Diptera, Tephritidae) with a pair of isolated apical spots
FIGURE 32. Tephritis theryi—habitus, paratype♀. Scale bar = 1 mm.
FIGURES 37a–f in Revision of the Old World species of the genus Tephritis (Diptera, Tephritidae) with a pair of isolated apical spots
FIGURES 37a–f. Tephritis youngiana new species: a—Paratype, habitus ♂; b–f—wing. Scale bar = 1 mm.
FIGURES 18a–b in Revision of the Old World species of the genus Tephritis (Diptera, Tephritidae) with a pair of isolated apical spots
FIGURES 18a–b. Tephritis heiseri: a—habitus ♀; b—abdomen, dorsal.
Supplementary material 2 from: Ney G, Schul J (2019) Epigenetic and genetic variation between two behaviorally isolated species of Neoconocephalus (Orthoptera: Tettigonioidea). Journal of Orthoptera Research 28(1): 11-19. https://doi.org/10.3897/jor.28.28888
: Explanation note: Matrix of MS-AFLP called fragments for all individuals.
Figure 5 from: Ney G, Schul J (2019) Epigenetic and genetic variation between two behaviorally isolated species of Neoconocephalus (Orthoptera: Tettigonioidea). Journal of Orthoptera Research 28(1): 11-19. https://doi.org/10.3897/jor.28.28888
Figure 5 Scatterplot of between-individual Euclidean genetic and epigenetic distance showing significant positive correlation between genetic and epigenetic differentiation. The correlation was tested using a Mantel test and 10,000 permutations of the design matrix to determine significance.
Figure 1 from: Ney G, Schul J (2019) Epigenetic and genetic variation between two behaviorally isolated species of Neoconocephalus (Orthoptera: Tettigonioidea). Journal of Orthoptera Research 28(1): 11-19. https://doi.org/10.3897/jor.28.28888
Figure 1 Species assignment based on call pulse period ratio and center frequency. Labeled boxes indicate the calls classified as N.robustus and N.bivocatus. Individuals that fall outside of species classifications were removed from further epigenetic and genetic analyses (as described in Ney and Schul 2017).
Figure 4 from: Ney G, Schul J (2019) Epigenetic and genetic variation between two behaviorally isolated species of Neoconocephalus (Orthoptera: Tettigonioidea). Journal of Orthoptera Research 28(1): 11-19. https://doi.org/10.3897/jor.28.28888
Figure 4 Consensus shared ancestry population structure for epigenetic and genetic loci. A. and C. Bar plots using MS-AFLP loci to estimate genetic (A) and epigenetic (C) structure among N.robustus and N.bivocatus using the software package STRUCTURE. B. and D. Delta K graphs for K = 1–10 genetic clusters showing moderate support for K = 2 genetic clusters (B) and low support for K = 4 epigenetic clusters (D).
Figure 3 from: Ney G, Schul J (2019) Epigenetic and genetic variation between two behaviorally isolated species of Neoconocephalus (Orthoptera: Tettigonioidea). Journal of Orthoptera Research 28(1): 11-19. https://doi.org/10.3897/jor.28.28888
Figure 3 PCoA of N.robustus and N.bivocatus utilizing genetic (A) and epigenetic (B) data. Plotted are the two most informative principal components calculated for the genetic and epigenetic loci datasets, as derived from the MS-AFLP fragment analysis. A. Genetic Euclidean distance with individuals grouped by species assignment. B. Epigenetic Euclidean distance with individuals grouped by species assignment. Group labels show the centroid of the points for each group. The long axis of the ellipse represents the direction of maximum dispersion and the short axis the direction of minimum dispersion.
Figure 2 from: Ney G, Schul J (2019) Epigenetic and genetic variation between two behaviorally isolated species of Neoconocephalus (Orthoptera: Tettigonioidea). Journal of Orthoptera Research 28(1): 11-19. https://doi.org/10.3897/jor.28.28888
Figure 2 Comparison of genome-wide methylation levels between species. Mann-Whitney U test; p<0.005 (**). Between-species significant variation is in total methylation (internal cytosine methylated and hemimethylated fragments).
Supplementary material 1 from: Wölfling M, Uhl B, Fiedler K (2019) Multi-decadal surveys in a Mediterranean forest reserve – do succession and isolation drive moth species richness? Nature Conservation 35: 25-40. https://doi.org/10.3897/natureconservation.35.32934
: Data type: species data
Figure 3 from: Poli A, Bovio E, Verkley G, Prigione V, Varese GC (2019) Elbamycella rosea gen. et sp. nov. (Juncigenaceae, Torpedosporales) isolated from the Mediterranean Sea. MycoKeys 55: 15-28. https://doi.org/10.3897/mycokeys.55.35522
Figure 3 Elbamycellarosea sp. nov.: 28-days-old colonies at 21 °C on ACMASWBCMASSC PDASW D PDASS; 28-days-old colonies at 10 °C on ECMASWFCMASSG PDASW H PDASS.
Figure 2 from: Poli A, Bovio E, Verkley G, Prigione V, Varese GC (2019) Elbamycella rosea gen. et sp. nov. (Juncigenaceae, Torpedosporales) isolated from the Mediterranean Sea. MycoKeys 55: 15-28. https://doi.org/10.3897/mycokeys.55.35522
Figure 2 Elbamycellarosea sp. nov. A, D group of young subglobose ascomata B, C globose ascomata with one or two necks E immature (bottom) and dehiscent (top) asci F ascoma in cross section G mature ascus with 8 ascospores H ascospores. Scale bars: 50 µm (A, D, F); 100 µm (B, C); 10 µm (E, G, H).
Figure 1 from: Poli A, Bovio E, Verkley G, Prigione V, Varese GC (2019) Elbamycella rosea gen. et sp. nov. (Juncigenaceae, Torpedosporales) isolated from the Mediterranean Sea. MycoKeys 55: 15-28. https://doi.org/10.3897/mycokeys.55.35522
Figure 1 Phylogenetic inference of Elbamycellarosea sp. nov. based on a combined nrSSU and nrLSU dataset. The tree is rooted to Xylariahypoxylon. Branch numbers indicate BPP/MLB values; Bar = expected changes per site (0.03).
Figure 2 from: Medina D, Ibáñez R, Lips KR, Crawford AJ (2019) Amphibian diversity in Serranía de Majé, an isolated mountain range in eastern Panamá. ZooKeys 859: 117-130. https://doi.org/10.3897/zookeys.859.32869
Figure 2 Individual-based rarefaction curves showing the estimated richness as a function of the upper 95% confidence interval (CI) calculated by the function Mao Tao. A Rarefaction curve combining all data obtained for the Serranía de Majé transect B rarefaction curves for low (120 – 150 m), intermediate (797 m), and high elevation (1,240–1,365 m) survey sites.
Figure 3 from: Medina D, Ibáñez R, Lips KR, Crawford AJ (2019) Amphibian diversity in Serranía de Majé, an isolated mountain range in eastern Panamá. ZooKeys 859: 117-130. https://doi.org/10.3897/zookeys.859.32869
Figure 3 Site-level dendrogram based on Jaccard dissimilarities and built with the unweighted pair-group method based on arithmetic averages (UPGMA). This analysis was based on all post-metamorphic amphibians captured at each site.
Figure 4 from: Medina D, Ibáñez R, Lips KR, Crawford AJ (2019) Amphibian diversity in Serranía de Majé, an isolated mountain range in eastern Panamá. ZooKeys 859: 117-130. https://doi.org/10.3897/zookeys.859.32869
Figure 4 Diagram showing a decrease with elevation in the similarities of amphibian species assemblages associated with sites from the Serranía de Piedras-Pacora mountain range and the isolated Serranía de Majé mountain range. The numbers represent the shared species between sites (N), Jaccard similarity coefficients (N) and total number of species at the site level (N). Each color represents an elevation category, where the lowlands (< 400 m) are represented in yellow, mid-elevation sites (400–800 m) in green, and highlands (> 800 m) in blue. NA = no data available.
Figure 1 from: Medina D, Ibáñez R, Lips KR, Crawford AJ (2019) Amphibian diversity in Serranía de Majé, an isolated mountain range in eastern Panamá. ZooKeys 859: 117-130. https://doi.org/10.3897/zookeys.859.32869
Figure 1 Map showing the location of the study sites in the Serranía de Majé and the Serranía de Piedras-Pacora across the valley of the Chepo River.
Supplementary material 1 from: Medina D, Ibáñez R, Lips KR, Crawford AJ (2019) Amphibian diversity in Serranía de Majé, an isolated mountain range in eastern Panamá. ZooKeys 859: 117-130. https://doi.org/10.3897/zookeys.859.32869
: Data type: specimen list.
Fig. 15 in Integrative taxonomy of five astome ciliates (Ciliophora, Astomatia) isolated from earthworms in Central Europe
Fig. 15. Small subunit rRNA gene phylogenetic trees showing systematic positions of astome ciliates isolated from lumbricid earthworms. Posterior probabilities were mapped onto the 50%-majority rule Bayesian consensus tree (upper panel) and bootstrap values onto the 50%-majority rule neighbor-joining tree (lower panel). Sequences in bold face were obtained during this study. Note that there is a conflict between the Bayesian and the neighbor-joining tree in the position of specimens of Metaradiophrya Jankowski, 2007. However, according to tree topology tests, the branching pattern of the Bayesian tree is not significantly better than that of the neighbor-joining tree. The scale bar denotes fraction of substitutions.
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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)
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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.