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Figure 4. A, Anokkostenostomum anatirostrum. B, A. corderoi. C, A. eveline. D, A in A taxonomic revision of South American species of the genus Stenostomum O. Schmidt (Platyhelminthes: Catenulida) based on morphological characters
Figure 4. A, Anokkostenostomum anatirostrum. B, A. corderoi. C, A. eveline. D, A. membrenosum. Scale bars = 200 Mm.
FIGURE 9. Nemadactylus macropterus, ANSP 102720, 213.8 in A taxonomic revision of Cheilodactylidae and Latridae (Centrarchiformes: Cirrhitoidei) using morphological and genomic characters
FIGURE 9. Nemadactylus macropterus, ANSP 102720, 213.8mm SL.
FIGURE 10. Pseudogoniistius nigripes, YPM 5957, 242.6 in A taxonomic revision of Cheilodactylidae and Latridae (Centrarchiformes: Cirrhitoidei) using morphological and genomic characters
FIGURE 10. Pseudogoniistius nigripes, YPM 5957, 242.6mm SL.
FIGURE 5. Dactylophora nigricans, USNM 84375, 338 in A taxonomic revision of Cheilodactylidae and Latridae (Centrarchiformes: Cirrhitoidei) using morphological and genomic characters
FIGURE 5. Dactylophora nigricans, USNM 84375, 338mm SL. Photograph by Sandra Raredon.
FIGURE 3. Cheilodactylus fasciatus, ROM 50995, 109 in A taxonomic revision of Cheilodactylidae and Latridae (Centrarchiformes: Cirrhitoidei) using morphological and genomic characters
FIGURE 3. Cheilodactylus fasciatus, ROM 50995, 109mm SL. Photograph by E Holm.
FIGURE 5 in The taxonomic revision of Asian Aristolochia (Aristolochiaceae) III: Two new taxa of Aristolochia and morphological revision for the flower character of A. obliqua from Yunnan, China
FIGURE 5. Holotype of Aristolochia hainanensis subsp. yingjiangensis (CSH-0134133).
FIGURE 3 in The taxonomic revision of Asian Aristolochia (Aristolochiaceae) III: Two new taxa of Aristolochia and morphological revision for the flower character of A. obliqua from Yunnan, China
FIGURE 3. Holotype of Aristolochia involuta (CSH-0137427).
TABLE 2. Diagnostic characters for X. lichneuta and X in Taxonomic status of Xyrosaris melanopsamma Meyrick, 1931 (Lepidoptera: Yponomeutidae) with notes on congeneric species in East Asia
<p><b>TABLE 2.</b> Diagnostic characters for <i>X. lichneuta</i> and <i>X. melanopsamma</i> on the base of female and male genitalia.</p><table><tbody><tr><th><b>No</b></th><th><b>Diagnostic character\ species</b></th><th><i>X. lichneuta</i></th><th><i>X. melanopsamma</i></th></tr><tr><th><b>Female genitalia</b></th></tr></tbody><tbody><tr><th>1</th><td>distance between anterior edge of sterigma and posterior edge of 7th segment</td><td>relatively short, 7.6 times shorter than papillae anales</td><td>relatively long, 2.5 times shorter than papillae anales</td></tr><tr><th>2</th><td>shape of posterior edge of 7th sternite</td><td>rounded concave, with distinct lateral triangular projections</td><td>almost straight, with faintly distinguishable lateral projections</td></tr><tr><th>3</th><td>shape of sterigma</td><td>transversely oval with distinct anterior margin</td><td>more or less angular, with a weakly defined anterior edge</td></tr><tr><th>4</th><td>7th sternite</td><td>with relatively wide longitudinal zone almost lacking microsetae in the middle and sclerotised lateral sides</td><td>with close longitudinal lines of dense microsetae in the middle and weak sclerotised lateral sides</td></tr><tr><th>5</th><td>plate between base of papillae anales</td><td>as equilateral triangle</td><td>as longitudinally elongated triangle</td></tr><tr><th><b>Male genitalia</b></th></tr><tr><th>6</th><td>length of harpa</td><td>reaches 9/10 of valva length</td><td>slightly exceeds 3/5 of valva length</td></tr><tr><th>7</th><td>row of strong thorns on apical part of harpa</td><td>semioval with equal dorsal and ventral parts (Fig. 8)</td><td>arched, with longer part along ventral margin of harpa (Fig. 12)</td></tr><tr><th>3</th><td>thorns on the apical part of harpa</td><td>smaller</td><td>larger, especially along ventral margin of harpa</td></tr><tr><th>4</th><td>shape of valva</td><td>smoothly widened from base towards 3/5 (Fig. 7)</td><td>smoothly widened from base towards 1/3, further parallel-sided towards 2/3 (Fig. 11)</td></tr></tbody></table><p>......continued on the next page</p>
FIGURE 2 in A revision of taxonomic relation between Oenothera royfraseri and O. turoviensis (sect. Oenothera, subsect. Oenothera; Onagraceae) based on multivariate analyses of morphological characters
FIGURE 2. The holotype of Oenothera turoviensis Rostański, sheet one of four (WRSL-4010207).
FIGURE 1 in A revision of taxonomic relation between Oenothera royfraseri and O. turoviensis (sect. Oenothera, subsect. Oenothera; Onagraceae) based on multivariate analyses of morphological characters
FIGURE 1. The lectotype of Oenothera royfraseri Gates (BM-1025692).
Fig. 51 in Phylogeny, Taxonomic Revision, And Character Evolution Of The Genera Chiasmocleis And Syncope (Anura, Microhylidae) In Amazonia, With Descriptions Of Three New Species
Fig. 51. Optimization (egg clutch size) and distribution (tadpole energy source and egg pigmentation) of some characters associated with reproductive biology of Chiasmocleis. Taxonomy updated to the one proposed in the present work. Chiasmocleis devriesi is nested within C. anatipes and is not shown.
Fig. 31 in Phylogeny, Taxonomic Revision, And Character Evolution Of The Genera Chiasmocleis And Syncope (Anura, Microhylidae) In Amazonia, With Descriptions Of Three New Species
Fig. 31. Distribution of Chiasmocleis hudsoni and C. haddadi. Star 5 type locality of C. jimi (considered here as a synonym of C. hudsoni); circles 5 examined specimens of C. hudsoni; cross 5 type locality of C. haddadi; half circles 5 examined specimens of C. haddadi.
Figure 6 from: Edgecombe G, Lopez Gutierrez B, MacLeod N (2011) Detecting taxonomic signal in an under-utilised character system: geometric morphometrics of the forcipular coxae of Scutigeromorpha (Chilopoda). ZooKeys 156: 49-66. https://doi.org/10.3897/zookeys.156.1997
Figure 6 - Strobe models of five positions along the canonical variates indicated in Fig. 5. CV-1, CV-2, and CV-3 axes account for 79.5% of the observed between-species shape variation. Landmarks and semi-landmarks are superimposed in the figure to the right of each sequence to express the magnitudes and directions (arrows) of shape trends. In all models, the mesial margin of the coxa is depicted to the left, the lateral margin to the right.
Figure 5 from: Edgecombe G, Lopez Gutierrez B, MacLeod N (2011) Detecting taxonomic signal in an under-utilised character system: geometric morphometrics of the forcipular coxae of Scutigeromorpha (Chilopoda). ZooKeys 156: 49-66. https://doi.org/10.3897/zookeys.156.1997
Figure 5 - Results of the CVA of coxal shape data for all eight species, showing the subspaces formed by the first three discriminant axes, which together account for more than 79% of observed between-group shape variation. Within each subspace plot the black circles represent the coordinate locations for each of the five along-axis shape models depicted in Fig. 6.
Figure 4 from: Edgecombe G, Lopez Gutierrez B, MacLeod N (2011) Detecting taxonomic signal in an under-utilised character system: geometric morphometrics of the forcipular coxae of Scutigeromorpha (Chilopoda). ZooKeys 156: 49-66. https://doi.org/10.3897/zookeys.156.1997
Figure 4 - Scatterplots of Procrustes PCA scores for coxal shape data. The first two shape variation axes (top) together account for 62.63% of the observed shape variation; PC-2 and PC-3 axes (bottom) together account for 27.58% of the observed shape variation.
Figure 3 from: Edgecombe G, Lopez Gutierrez B, MacLeod N (2011) Detecting taxonomic signal in an under-utilised character system: geometric morphometrics of the forcipular coxae of Scutigeromorpha (Chilopoda). ZooKeys 156: 49-66. https://doi.org/10.3897/zookeys.156.1997
Figure 3 - Thereuopoda longicornis scatterplot of coxal shape data along the discriminant subspace formed by the first two CV axes, which together account for 74.17% of observed between-group shape variation.
Figure 2 from: Edgecombe G, Lopez Gutierrez B, MacLeod N (2011) Detecting taxonomic signal in an under-utilised character system: geometric morphometrics of the forcipular coxae of Scutigeromorpha (Chilopoda). ZooKeys 156: 49-66. https://doi.org/10.3897/zookeys.156.1997
Figure 2 - Landmarks (L1-L10) used in morphometric analysis. Diagonal line to L1 is the longest line from anterolateral to posteromedial corners of the coxa. Spine-bristles numbered 1-4 (blue) from interior to exterior. Throughout text, left and right coxae refer to dorsal orientation (inverted 180° relative to this ventral view).
Figure 1 from: Edgecombe G, Lopez Gutierrez B, MacLeod N (2011) Detecting taxonomic signal in an under-utilised character system: geometric morphometrics of the forcipular coxae of Scutigeromorpha (Chilopoda). ZooKeys 156: 49-66. https://doi.org/10.3897/zookeys.156.1997
Figure 1 - Ventral view of head and forcipules of Thereuopoda longicornis placed in a standard horizontal position. BM 1952.9.8.574-575, Kuching, Sarawak, Malaysia.
Figure 26 from: Syaukani S, Thompson G (2011) Taxonomic Notes on Nasutitermes and Bulbitermes (Termitidae, Nasutitermitinae) from the Sunda region of Southeast Asia based on morphological and molecular characters. ZooKeys 148: 135-160. https://doi.org/10.3897/zookeys.148.2055
Figure 26 - Figure 26. Plot of maximum intraspecific divergence against nearest neighbour distance between species (Bulbitermes 4 spp. and Nasutitermes 4 spp.) as identified from morphological characters. All species fall above the 1:1 line, indicating the presence of a barcode gap.
Figures 9-16 from: Syaukani S, Thompson G (2011) Taxonomic Notes on Nasutitermes and Bulbitermes (Termitidae, Nasutitermitinae) from the Sunda region of Southeast Asia based on morphological and molecular characters. ZooKeys 148: 135-160. https://doi.org/10.3897/zookeys.148.2055
Figures 9-16 - Figures 9–16. Workers of Bulbitermes from Sunda region. Left 9, 11, 13, 15 and right 10, 12, 14, 16 mandibles. B. constrictus 9, 10 B. singaporiensis 11, 12 B. flavicans 13, 14 B. neopusillus 15, 16. Scale bar: 0.1 mm.
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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.