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FIGURE 10 in Taxonomy of the Brazilian species previously placed in Mantispa Illiger, 1798 (Neuroptera: Mantispidae), with the description of three new species
FIGURE 10. Dicromantispa hyalina: male: a, abdominal tergites; b, sternite IX, ventral view; c, terminalia, dorsal view; d, gonarcus, posterior view; e, ventromedial lobe; f, genitalia, ventral view; g, genitalia, lateral view. gonarcal lateral lobe (gll). Scale = 0.1 mm, except for a.
FIGURE 22 in Taxonomy of the Brazilian species previously placed in Mantispa Illiger, 1798 (Neuroptera: Mantispidae), with the description of three new species
FIGURE 22. Leptomantispa axillaris: male: a, abdominal tergites; b, terminalia, dorsal view; c, sternite IX, ventral view; d, gonarcus, dorsal view; e, genitalia, ventral view; f, genitalia, lateral view; female: g, fertilization canal; h, sternite VIII, ventral view; i, spermatheca; j, terminalia, lateral view. Gonarcal membrane (gm), hypomere (hp). Scale = 0.1 mm, except for a.
FIGURE 6 in Taxonomy of the Brazilian species previously placed in Mantispa Illiger, 1798 (Neuroptera: Mantispidae), with the description of three new species
FIGURE 6. Dicromantispa debilis: male: a, abdominal tergites; b, terminalia, dorsal view; c, sternite IX, ventral view; d, gonarcus, posterior view; e, genitalia, ventral view; f, genitalia, lateral view; female: g, fertilization canal; h, sternite VIII, ventral view; i, spermatheca; j, terminalia, lateral view. Capsule (cap), fertilization canal duct (fcd), gonarcal membrane (gm), hypomere (hp), pore (po), pseudopenal membrane (ppm), scar (sc), ventromedial lobe (vml). Scales = 0.1 mm, except for a.
FIGURE 8 in Taxonomy of the Brazilian species previously placed in Mantispa Illiger, 1798 (Neuroptera: Mantispidae), with the description of three new species
FIGURE 8. Dicromantispa gracilis: male: a, abdominal tergites; b, terminalia, dorsal view; c, ectoproct, ventral view; d, sternite IX, ventral view; e, genitalia, ventral view; f, genitalia, lateral view; g, gonarcus, posterior view; female: h, sternite VIII, ventral view; i, spermatheca; j, terminalia, lateral view. Gonarcus (gnc), sternite (stn), ventromedial lobe (vml). Scale = 0.1 mm, except for a.
FIGURE 4 in Taxonomy of the Brazilian species previously placed in Mantispa Illiger, 1798 (Neuroptera: Mantispidae), with the description of three new species
FIGURE 4. Buyda phthisica: male: a, ectoproct, lateral view; b, gonarcus, dorsal view; c, sternite IX, ventral view; d, terminalia, dorsal view; e, genitalia, ventral view; f, genitalia, lateral view; g, hypomere; female: h, sternite VIII, ventral view; i, spermatheca; j, terminalia, lateral view. Bursa copulatrix (bcp), ectoproct (ect), fertilization canal (fc), gonocoxite (gcx), gonarcal membrane (gm), gonarcal median lobe (gml), gonarcus (gnc), hypomere (hp), mediuncus (med), pseudopenis (pp), spermathecal duct (spd), sternite (stn), ventromedial lobe (vml). Scales = 0.1 mm.
Figs. 12–15. Stenocrates popei, parameres. 12–13 in A Revised Catalog of the Species ofStenocratesBurmeister (Coleoptera: Scarabaeidae: Dynastinae: Cyclocephalini), with Descriptions of Three New Species from Peru and Brazil andStenocrates inpaiRatcliffe, 1978 Placed in Junior Synonymy withStenocrates popeiEndrödi, 1971
Figs. 12–15. Stenocrates popei, parameres. 12–13) As illustrated by Endrödi (1985); 14–15) More detailed illustration.
Figs. 3–6. Stenocrates species, parameres. 3 in A Revised Catalog of the Species ofStenocratesBurmeister (Coleoptera: Scarabaeidae: Dynastinae: Cyclocephalini), with Descriptions of Three New Species from Peru and Brazil andStenocrates inpaiRatcliffe, 1978 Placed in Junior Synonymy withStenocrates popeiEndrödi, 1971
Figs. 3–6. Stenocrates species, parameres. 3) S. howdeni; 4) S. laborator; 5–6) S. hastatus. Illustrations in Figs. 3–4 from Dechambre and Hardy (2004).
FIGURE 4 in A new species of the genus Dibamus Duméril & Bibron, 1839 (Squamata: Dibamidae) from the driest and hottest place of Vietnam
FIGURE 4. Skeletal morphology of the male paratype of Dibamus tropcentr sp. nov. (ZMMU Re-17444). General view of the skeleton (A); skull in ventral (B), dorsal (C), and lateral (D) views; skeletal structures present in the cloacal region in lateral view (E), vertebral column shaded. Terminology follows Greer (1985) and Rieppel (1984). Notes: *—exoccipital fused with opisthotic; **—compound bone consists of fused splenial, articular, angular, and supraangular bones (Greer 1985).
FIGURE 5 in A new species of the genus Dibamus Duméril & Bibron, 1839 (Squamata: Dibamidae) from the driest and hottest place of Vietnam
FIGURE 5. Natural macrohabitat (A) and microhabitat (B) of Dibamus tropcentr sp. nov. at the type locality in Da Vach Mountain, Nui Chua National Park, Ninh Thuan Province, Vietnam. The rotten log shown in (B) was the habitat where the holotype of the new species was found together with Globitermes sulphureus (Haviland) colony. Photographs by Nikolay A. Poyarkov.
FIGURE 2 in A new species of the genus Dibamus Duméril & Bibron, 1839 (Squamata: Dibamidae) from the driest and hottest place of Vietnam
FIGURE 2. Holotype of Dibamus tropcentr sp. nov. (ZMMU Re-17443, female) in life in situ (A) and prior to preservation (B). Photographs by Nikolay A. Poyarkov. Scale bar equals 5 mm.
FIGURE 1 in A new species of the genus Dibamus Duméril & Bibron, 1839 (Squamata: Dibamidae) from the driest and hottest place of Vietnam
FIGURE 1. Distribution of the genus Dibamus in southern Indochina. Dot in a center of an icon marks the type locality of a species. Localities: Laos: 1—Pakxong District, Champasak Province (FMNH 258662); Vietnam: 2—Sao La Nature Reserve, A Luoi District, Thua Thien – Hue Province (Nguyen et al. 2009); 3—Son Tra Nature Reserve, Da Nang City (Phan et al. 2021); 4—Ngoc Linh Nature Reserve, Kon Tum Province (Le et al. 1999); 5—Kon Chu Rang Nature Reserve and Tram Lap, Gia Lai Province (Darevsky 1992); 6—Buon Luoi, Gia Lai Province (Darevsky 1992); 7—Da Ban Lake, Ninh Hoa District, Khanh Hoa Province (Greer 1985; Darevsky 1992; note: this locality may also refer to the environs of D'Ran Town, Don Duong District, Lam Dong Province); 8—Hon Ba Nature Reserve, Khanh Hoa Province (Bobrov 2008); 9—Le Bosquet, Da Lat City, Lam Dong Province (Smith 1921); 10—Nui Chua National Park, Ninh Thuan Province (this work); 11—Binh Chau – Phuoc Buu Nature Reserve, Ba Ria – Vung Tau Province (Ineich 1999); 12—Con Dao National Park, Ba Ria – Vung Tau Province (Honda et al. 2001); Cambodia: 13—Dalai Mountain, Phnom Samkos Wildlife Sanctuary, Pursat Province (Neang et al. 2011); Thailand: 14—Khao Soi Dao Wildlife Sanctuary, Chanthaburi Province (Honda et al. 1997). The thumbnail represents the holotype of Dibamus tropcentr sp. nov. in life (ZMMU Re-17443, female); photograph by Nikolay A. Poyarkov.
FIGURE 3 in A new species of the genus Dibamus Duméril & Bibron, 1839 (Squamata: Dibamidae) from the driest and hottest place of Vietnam
FIGURE 3. Photographs (A–C) and line drawings (D–F) of head scalation of the holotype of Dibamus tropcentr sp. nov. (ZMMU Re-17443, female), and line drawings (G–I) of the paratype of Dibamus smithi (NHMUK 1946.8.21.24, female). Head is shown in lateral (A, D, G), ventral (B, E, H), and dorsal (C, F, I) aspects. Scale bar equals 1 mm. Small dots on the rostral and labial area indicate sensory papillas. Photographs A–C and line drawings D–F by Nikolay A. Poyarkov; line drawings G–I modified from Greer (1985).
Fig. 1 in Eponyms have no place in 21st-century biological nomenclature
Fig. 1 | Number of eponym species in relation to the commemorated person's profession and/or relation to the describing author. The y axis refers to the commemorated person's nationality.Data refer to birds16, mammals17, amphibians18 and reptiles19 in Africa.
Fig. 2 in Eponyms have no place in 21st-century biological nomenclature
Fig. 2 | Proportions of eponym species in Africa and origins of their names. Percentages are those of eponym species in relation to the total number of species for land vertebrate taxa (amphibians,birds,mammals and reptiles),by African country.Pie charts show the national origins of eponyms for selected countries.Patterns in species eponyms often reflect histories of colonialism and imperialism specific to individual countries (for example, the prevalence of Belgian-derived eponyms in the Democratic Republic of the Congo or of Italianderived eponyms in Libya).
Céramiques trouvées place du 11 Novembre à Laval
Source: Objaverse 1.0 / Sketchfab
Fig. (2). Distribution of responses regarding the place of eating.
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TV Dictionary - Peyton Place (video essay)
<p>The classic TV soap opera PEYTON PLACE in just one word. With a little help from Merriam-Webster and Gilles Deleuze.</p>
Subspecies and Distribution. L. lL. lagothricha Humboldt, 1812 — SE Colombia, NE Ecuador, NW Brazil, and N Peru, from the Cordillera Oriental, N of the rios Napo and Amazonas, to the Rio Uva, a N bank affluent of the Rio Guaviare (Vichada Department, Colombia), E to the Rio Orinoco and upper Rio Negro to the Venezuelan border and NW Brazil; it is not known if it occurs in Venezuela. L. [. lugens Elliot, 1907 — Colombia, E of the Rio Atrato, throughout the Cordillera Oriental, W of the Rio Ariari (Meta Department), and parts of the Cordillera Central to the northernmost parts of the Serrania de San Lucas (SE Bolivar & N Antioquia departments), in some places up to elevations of 3000 m, and northward in the piedmont forest (now mostly destroyed) to the Rio Arauca (Arauca Department); there is no evidence thatits occurs in neighboring SW Venezuela. in Atelidae
Subspecies and Distribution. L. lL. lagothricha Humboldt, 1812 — SE Colombia, NE Ecuador, NW Brazil, and N Peru, from the Cordillera Oriental, N of the rios Napo and Amazonas, to the Rio Uva, a N bank affluent of the Rio Guaviare (Vichada Department, Colombia), E to the Rio Orinoco and upper Rio Negro to the Venezuelan border and NW Brazil; it is not known if it occurs in Venezuela. L. [. lugens Elliot, 1907 — Colombia, E of the Rio Atrato, throughout the Cordillera Oriental, W of the Rio Ariari (Meta Department), and parts of the Cordillera Central to the northernmost parts of the Serrania de San Lucas (SE Bolivar & N Antioquia departments), in some places up to elevations of 3000 m, and northward in the piedmont forest (now mostly destroyed) to the Rio Arauca (Arauca Department); there is no evidence thatits occurs in neighboring SW Venezuela.
Figure 1 in Evidence from mitochondrial genomics supports the lower Mesozoic of South Asia as the time and place of basal divergence of cypriniform fishes (Actinopterygii: Ostariophysi)
Figure 1. Geographical regions of cypriniform fish distribution at the continental scale. The seven region scheme presented here [Africa (Af), South Asia (Sa), East Asia (Ea), Europe (Eu), Siberia (Sb), and western and eastern North America (Wn & En)] is a modification of the conventional Wallace's six region system (Berra, 2001). East Asia, Europe, and Siberia are subdivisions of the Palaearctic region, overlapping with each other. Western and eastern North America are subdivisions of the Nearctic region.
Figure 5. A in Evidence from mitochondrial genomics supports the lower Mesozoic of South Asia as the time and place of basal divergence of cypriniform fishes (Actinopterygii: Ostariophysi)
Figure 5. A reconciled dispersal-vicariance analysis (DIVA; upper) and a simple parsimonious reconstruction (lower) inference of past ranges at the subfamilial level superimposed over divergence time estimates. Open rectangular bars stand for 95% confidence ranges of the divergence time estimates. The scale bar at the bottom represents the geological time scale according to Gradstein, Ogg & Smith (2004). Maps drawn from Smith, Smith & Funnel (1994) indicate onset (220 Mya) and completion (160 Mya) of the Pangaean breakup, and separation of the Indian land mass from Africa (130 Mya), which allowed marine permeation. Arrowheads indicate rifting margins; hatched pattern indicates area of black shale deposits (Olsen, 1997).
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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.