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9,937 results for “Endemicity”
Fig. 6 in New genera of stiletto flies endemic to Madagascar (Therevidae: Therevinae)
Fig. 6. Rinhatiana distincta (Lyneborg, 1976) comb. nov., ♀, (CSCA). A. Lateral view. B. Oblique view.
Figure 9 in Description of a new endemic genus of the Namib Desert and adjacent biomes in Namibia (Tineoidea: Tineidae: Hapsiferinae)
Figure 9 – Rooiklipia spec., female genitalia, A: R. mirabib, ventral; B–C: R. michaelmeyi spec. nov., B: ventral, C: lateral.
Figure 11 in Description of a new endemic genus of the Namib Desert and adjacent biomes in Namibia (Tineoidea: Tineidae: Hapsiferinae)
Figure 11 – Landscape at Rooiklip guest farm, dry season 2019, with Gamsberg (2349 m) in the background.
Figure 13 in Description of a new endemic genus of the Namib Desert and adjacent biomes in Namibia (Tineoidea: Tineidae: Hapsiferinae)
Figure 13 – Best RAxML tree topology of the COI-5P fragment, with bootstrap values displayed above nodes.
DATASET Stridulation sounds of the pacamã Lophiosilurus alexandri Steindachner, 1876 (Pseudopimelodidae), a threatened endemic Brazilian catfish
<p>This dataset contains acoustic files with sounds produced by the pacamã Lophiosilurus alexandri Steindachner, 1876. The details can be found in the related publication Raick et al. 2025.</p>
Table 1 in Evolution of Impatiens (Balsaminaceae) in the Albertine Rift – The endemic Impatiens purpureoviolacea complex consists of ten species
<p><b>Table 1.</b> Sequence characterstics of each datamatrix.</p><table><tbody><tr><th></th><th>Taxa</th><th>Characters</th><th>Parsimony-informative characters</th><th>Variable characters</th><th>Consistency index</th><th>Retention index</th></tr></tbody><tbody><tr><th><i>atpB-rbcL</i></th><td>17 + 1*</td><td>729</td><td>2</td><td>15</td><td>1</td><td>1</td></tr><tr><th><i>ImpDEF1/ImpDEF2</i></th><td>18 + 2(1)*#</td><td>1023</td><td>43</td><td>145</td><td>0.95</td><td>0.92</td></tr><tr><th>Combined</th><td>18</td><td>1752</td><td>45</td><td>160</td><td>0.95</td><td>0.93</td></tr></tbody></table><p>Consistency index: Kluge & Farris (1969), retention index: Farris (1989).</p><p>* indicates inclusion of the hybrid accession, <sup>#</sup> indicates inclusion of two copies of the nuclear genes <i>ImpDEF1</i> and <i>ImpDEF2</i> of the hybrid accession.</p>
FIG. 11 in Biodiversity of bathyal coral gardens - portrait of a uniserial bryozoan endemic to the South Azorean Seamount Chain: an unexpected evolutionary testbed?
FIG. 11. — Epifaunal assemblage associated to Madrepora oculata Linnaeus, 1758 on the bathyal slope off Brittany. Reproduction of plate 6 of the book "Les profondeurs de la mer'' by Y. Le Danois (1948), Payot, Paris.
FIG. 10 in Biodiversity of bathyal coral gardens - portrait of a uniserial bryozoan endemic to the South Azorean Seamount Chain: an unexpected evolutionary testbed?
FIG. 10. — Harmelinius uniserialis (Harmelin, 1978), intramural budding: A, two old AZ and a KZ showing marks of repeated intramural budding; B, distal part of an old AZ with multiple nested calcified layers reducing the size of the orifice and of the opesia of the avicularium; C, AZ with lateral wall presenting several nested calcified layers; D, same AZ, proximal part of the costal shield and nested layers of the lateral wall; E, same AZ, distal part showing the reduced size of the orifice and the foramen; F, old AZ with a closure plate below the damaged costal shield; G, cystid of an old damaged AZ filled with a KZ with a central window; H, distal part of a colony covered by calcified deposits produced by tissues of a corallite of Solenosmilia variabilis Duncan, 1873. Origin: A, B, F, G, Hyères SMT, Stn DW 184; C, D, E, Hyères SMT, Stn DW 200; H, Tyro SMT, Stn DW 276. Scale bars: A, 200 µm; B, D, E, 50 µm; C, F, G, 100 µm; H, 400 µm.
FIG. 6 in Biodiversity of bathyal coral gardens - portrait of a uniserial bryozoan endemic to the South Azorean Seamount Chain: an unexpected evolutionary testbed?
FIG. 6. — Harmelinius uniserialis (Harmelin, 1978), different types of avicularia: A, "adnate" type (AV3) on an ovicelled AZ; B, "columnar" type (AV1); C, "giant" type (AV5) with three porous knobs, one incompletely formed, distal to the slightly prominent rostrum; D, "adnate" type, adventitious to an ovicelled AZ, with a large pore chamber and three porous knobs (inset: enlarged view of a knob); E, autozooid with five "pyramidal" morphs (AV4) budded from lateral walls; F, vicarious kenozooid with thickened cuticule persisting on the frontal gymnocyst and the central window; G, globular and pyramidal avicularia budded by the same AZ; H, three globular (AV2), one "giant" (AV5) and one "pyramidal" (AV4) avicularia budded by two AZ and a vicarious KZ with persistent cuticular layer; Origin: A, D, Tyro SMT, Stn DW 276; B, Hyères SMT, Stn DW 200; C, E, F, G, H, Tyro SMT, Stn DW 278. Scale bars: B, C, D, 50 µm; A, F, G, 100 µm; D, H, 200 µm.
FIG. 5 in Biodiversity of bathyal coral gardens - portrait of a uniserial bryozoan endemic to the South Azorean Seamount Chain: an unexpected evolutionary testbed?
FIG. 5. — Harmelinius uniserialis (Harmelin, 1978), structure of the ovicell: A, distal part of an ovicelled autozooid bearing two adnate avicularia (AV3), with open medial slit, and ooecial kenozooid budding a distal zooid; B, close-up of the same ovicell, medial slit showing the two layers of the bivalved ooecial wall, the dorsal window of the distal kenozooid with thick gymnocystal layers and oval opesia, and two lateral porous knobs; C, ovicell in formation showing the floor of the brood chamber budded by the maternal autozooid; D, broken ovicell showing the thickness of the frontal wall and the two proximal layers, and the foramen open through the transverse wall. Origin: A, B, C, Tyro SMT, Stn DW 276; D, Hyères SMT, Stn DW 184. Scale bars: A, C, D, 100 µm; B, 50 µm.
FIG. 1 in Biodiversity of bathyal coral gardens - portrait of a uniserial bryozoan endemic to the South Azorean Seamount Chain: an unexpected evolutionary testbed?
FIG. 1. — Geographical location and depth distribution of the 19 sampling stations of Harmelinius uniserialis (Harmelin, 1978). Abbreviations: AT, Atlantis Seamount; IR, Irving Seamount; HY, Hyères Seamount; ME, Great Meteor Seamount; PL, Plato Seamount; SM, Azores, São Miguel; TY, Tyro Seamount. Map downloaded from GEBCO 2019 Gridded Bathymety Data.
FIG. 9 in Biodiversity of bathyal coral gardens - portrait of a uniserial bryozoan endemic to the South Azorean Seamount Chain: an unexpected evolutionary testbed?
FIG. 9. — Harmelinius uniserialis (Harmelin, 1978), vicarious kenozooids: A, drawing of two interconnected KZ, laterally budded by 2 AZ; B, light photography of the same zooids; C, part of colony with seven variously shaped KZ connected to several AZ; D, two differently sized KZ budded from the lateral walls of two AZ; E, pentagonal KZ with proximal corner folded on the budding locus of the maternal zooid; F, frontal wall of a large KZ with central window open on a thick, multilayered wall, surrounded by seven porous knobs. Distansescharella d'Orbigny, 1853: G, D. alcicornis (Jullien, 1882), large vicarious KZ with central window, abutted on to an AZ and close to an adventitious avicularium; H, D. seguenzai Cipolla, 1921, reticulum formed by three small KZ with a central window surrounded by 2-5 conical spinous processes with a likely porous tip; I, D. alcicornis, avicularium with opesia and rostrum poorly differentiated, and proximal side folded on the maternal zooid. Origin: A, B, Azores, São Miguel bathyal slope, Biaçores Stn 197, 815 m (9A copied from Harmelin 1978, fig. 2); C, F, Hyères SMT, Stn DW 200; D, E, Tyro SMT, Stn DW 276; G, I, R/V Thalassa, Y434, 620 m, on Lophelia prolifera (Linnaeus, 1758); H, R/V Calypso, Stn 1902, Libya. Scale bars: A, B, D, F, 200 µm; C, 400 µm; E, G, H, 100 µm; I, 50 µm.
FIG. 4 in Biodiversity of bathyal coral gardens - portrait of a uniserial bryozoan endemic to the South Azorean Seamount Chain: an unexpected evolutionary testbed?
FIG. 4. — Harmelinius uniserialis (Harmelin, 1978), morphology of non ovicelled autozooids and ancestrula: A, autozooid (AZ) with two avicularia (AV1) and distal budding from the kenozooidal cap, budded from the lateral side of another AZ; B, AZ distal part with a AV1 avicularium, note the foramen through the transverse wall separating the AZ orifice from the kenozooidal cap (idem in A), the concave proximal edge of the orifice and the unequal size of costae; C, eroded kenozooidal cap showing its subconical chamber and the broken base of the AZ transverse wall; D, distal part of AZ showing the boundary between the kenozooidal cap and the orifice frame; E, ancestrula and AZ, note their contrasting sizes and the proximal budding by the ancestrula. Origin: A, B, C, Hyères SMT, Stn DW 200; D, E, Tyro SMT, Stn DW 276. Scale bars: A, B, E, 200 µm; C, D, 100 m.
FIG. 8 in Biodiversity of bathyal coral gardens - portrait of a uniserial bryozoan endemic to the South Azorean Seamount Chain: an unexpected evolutionary testbed?
FIG. 8. — Harmelinius uniserialis (Harmelin, 1978), drawings of five types of avicularia: A, "adnate" (AV3); B, "pyramidal" (AV4); C, "giant" (AV5); D, "columnar" (AV1); E, "globular" (AV2). Origin: copied from diverse SEM pictures. Scale bar: 50 µm.
FIG. 2 in Biodiversity of bathyal coral gardens - portrait of a uniserial bryozoan endemic to the South Azorean Seamount Chain: an unexpected evolutionary testbed?
FIG. 2. — Harmelinius uniserialis (Harmelin, 1978), colonized substrates and general aspect of colonies: A, fragment of Madrepora oculata Linnaeus,1758; B, pebble; C, part of colony showing non-caudate autozooids, optical view; D, other aspect of the same colony, SEM view; E, part of colony with typical features. Origin: A, C, D, Hyères SMT, Stn DW 184; B, Irving SMT, Stn DW 251; E, Tyro SMT, Stn DW 276. Scale bars: A, B, 1 cm; C, D, 1 mm; E, 400 µm.
FIG. 7. — A in Biodiversity of bathyal coral gardens - portrait of a uniserial bryozoan endemic to the South Azorean Seamount Chain: an unexpected evolutionary testbed?
FIG. 7. — A, Glabrilaria pedunculata (Gautier, 1956), ovicelled zooid crowned by seven pedunculate avicularia; B, Cribrilaria cassidainsis Harmelin, 1984, colony edge with ten interzooidal avicularia. Origin: A, B, Mediterranean Sea, France, La Ciotat, 3PP Cave, 40-60 m inside; A, B, 20-24 m depth. Scale bars: A, 100 µm; B, 200 µm.
FIG. 3 in Biodiversity of bathyal coral gardens - portrait of a uniserial bryozoan endemic to the South Azorean Seamount Chain: an unexpected evolutionary testbed?
FIG. 3. — Harmelinius uniserialis (Harmelin, 1978), structure of colonies and graphs of zooid proportions: A - a, distal budding of autozooids with long cauda; b, lateral budding of autozooid (AZ) and kenozooid (KZ); c, abutment of kenozooid on ovicelled AZ - 1, KZ (21% white), non-ovicelled AZ (78% grey), ovicelled AZ (1% black); 2, non ovicelled AZ without avicularium (AV) (59% white), with one AV (24% grey), with two AV (17% dark); 3, ovicelled AZ, with one AV (23% grey), with two AV (77% dark); B, ovicellar kenozooid connected to the lateral pore chamber of an adjacent AZ; C, zooidal aggregation with 12 AZ without cauda, 28 AV and three KZ; D, clustering of three AZ without cauda, involving a small vicarious kenozooid abutted on to an avicularium (AV4) in proximal position, co-occurring with another AV type (AV2); E, dense aggregation of KZ. Origin: A, B, Tyro SMT, Stn DW 276; C, D, E, Tyro SMT, Stn DW 278. Scale bars: A, C, E, 400 µm; B, D, 200 µm.
Figure 3 in Phylogenetic measures of biodiversity and neo- and paleo-endemism in Australian Acacia
Figure 3 | CANAPE, a two-step procedure described in text. (a) Map of centres of endemism discovered. White cells contain no records; beige cells are not significant. The red values indicate grid cells that contain significantly lower RPE than expected given random sampling of the same number of species from a null tree, termed 'centres of neo-endemism'. The blue values indicate grid cells that contain significantly higher RPE than expected, termed 'centres of paleo-endemism'. The purple values indicate grid cells that are a mix of neo-endemism and paleo-endemism; the most highly significant of which (darker purple) are termed 'centres of superendemism'. (b) Bivariate plot showing the relationship between the numerator (y axis) and denominator (x axis) of RPE, applied following the two-step CANAPE procedure described in text, for comparison with a. The grey points in the background are results of the randomization, the beige points are actual values for grid cells that are not significant, the red points are actual values for grid cells that are interpreted as significantly dominated by neo-endemism, the blue points are actual values for grid cells that are interpreted as significantly dominated by paleo-endemism, and the purple points are actual values for grid cells significant for both the y-axis and x-axis variables separately, the most highly significant of which (darker purple) are termed 'centres of super-endemicity'.
Figure 2 in Phylogenetic measures of biodiversity and neo- and paleo-endemism in Australian Acacia
Figure 2 | Maps showing significance levels resulting from of a randomization test in Australian Acacia. White cells contain no records; beige cells are not significant. (a) PD: the red values indicate grid cells that contain significantly less PD than expected; the blue values indicate grid cells that contain significantly more PD than expected. (b) RPD: the red values indicate grid cells that contain significantly less RPD than expected; the species present in that cell are significantly more closely related than expected. The blue values indicate grid cells that contain significantly more RPD than expected; the species present in that cell are significantly more distantly related than expected. (c) Phylogenetic endemism (PE). The red values indicate grid cells that contain significantly less PE than expected; the blue values indicate grid cells that contain significantly more PE than expected. (d) Relative phylogenetic endemism (RPE). The red values indicate grid cells that contain significantly lower RPE than expected; the blue values indicate grid cells that contain significantly higher RPE than expected.
Fig. 3. – Virotia azurea H.C. Hopkins & Pillon. A in Virotia azurea (Proteaceae: Macadamieae), a striking new species endemic to New Caledonia and notes on V. francii and V. leptophylla
Fig. 3. – Virotia azurea H.C. Hopkins & Pillon. A. Fruit; B. Fruit cut open to reveal the bluish mauve cotyledons. [Photos: G. Gâteblé]
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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.