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Figures 8-13 from: Zonstein SL, Marusik YM, Omelko MM (2016) Redescription of the type species of Diaphorocellus Simon, 1893 (Araneae, Palpimanidae, Chediminae). African Invertebrates 57(2): 93-103. https://doi.org/10.3897/AfrInvertebr.57.9988
Figures 8-13 - Diaphorocellus biplagiatus. 8 eye pattern in female, dorsal 9 epigastric scutum, female, ventral 10 epigastric scutum after maceration, caudal view 11–13 male palp, prolateral, ventro-prolateral and retrolateral. Abbreviations: Bs sclerite opposite to book lungs; Cs strong cymbial setae; Em "embolus"; Gg grape-shaped gland; Ls lateral sclerite; Mo membranous outgrowth; Ms median sclerite; Re receptacle; So sclerotised outgrowth.
Figures 1-7 from: Zonstein SL, Marusik YM, Omelko MM (2016) Redescription of the type species of Diaphorocellus Simon, 1893 (Araneae, Palpimanidae, Chediminae). African Invertebrates 57(2): 93-103. https://doi.org/10.3897/AfrInvertebr.57.9988
Figures 1-7 - Habitus of Diaphorocellus biplagiatus male (1, 4–5, 7) and female (2–3, 6). 1, 3 entire body, dorsal 2, 7 prosoma and anterior part of abdomen, ventral 5–6 prosoma, dorsal.
Figure 27 from: Zonstein SL, Marusik YM, Omelko MM (2016) Redescription of the type species of Diaphorocellus Simon, 1893 (Araneae, Palpimanidae, Chediminae). African Invertebrates 57(2): 93-103. https://doi.org/10.3897/AfrInvertebr.57.9988
Figure 27 - Distribution of Diaphorocellus biplagiatus. The type locality (open circle) and new records listed in the text (solid circles).
Figures 20-26 from: Zonstein SL, Marusik YM, Omelko MM (2016) Redescription of the type species of Diaphorocellus Simon, 1893 (Araneae, Palpimanidae, Chediminae). African Invertebrates 57(2): 93-103. https://doi.org/10.3897/AfrInvertebr.57.9988
Figures 20-26 - Details of endogyne of Diaphorocellus biplagiatus. 20 dorsal 21 basal part, caudal-dorsal 22 grape-shaped glands 23 base of receptacles, dorsal 24 tip of base showing cilia 25 lateral part of receptacle base showing grape-shaped glands and fine threads 26 terminal part of receptacle base 21–26 made by transmitting microscope. Abbreviations: Cg cilia of Gg; Da dark area of Sb; Ft fine threads; Gg grape-shaped gland; Rs membranous sac like part of Re; Sb complex sclerotised base of Re.
Figure 1c from: Gutiérrez EE, Helgen KM, McDonough MM, Bauer F, Hawkins MTR, Escobedo-Morales LA, Patterson BD, Maldonado JE (2017) A gene-tree test of the traditional taxonomy of American deer: the importance of voucher specimens, geographic data, and dense sampling. ZooKeys 697: 87-131. https://doi.org/10.3897/zookeys.697.15124
Figure 1c - Phylogenetic tree of cytochrome-b sequences of Odocoileini (continuation). This is a strict consensus topology resulting from the Bayesian inference analysis. Nodal support is indicated at each node, except where the relationship received negligible support. Posterior probabilities (from the Bayesian inference analysis) and bootstrap values (from the maximum-likelihood analysis) are indicated before and after the slashes ("/") at branches of interest (i.e., nodal support for fairly shallow relationships within intraspecific haplogroups are omitted). The scale represents substitutions per site. For each terminal, country of origin and next-largest administrative unit (state, department, province, etc.) are provided (when reported by the team that generated them; see detailed voucher and locality information in supplementary file 1 for sequences that we generated). GenBank accession numbers are indicated for each terminal.
Figure 1b from: Gutiérrez EE, Helgen KM, McDonough MM, Bauer F, Hawkins MTR, Escobedo-Morales LA, Patterson BD, Maldonado JE (2017) A gene-tree test of the traditional taxonomy of American deer: the importance of voucher specimens, geographic data, and dense sampling. ZooKeys 697: 87-131. https://doi.org/10.3897/zookeys.697.15124
Figure 1b - Phylogenetic tree of cytochrome-b sequences of Odocoileini (continuation). This is a strict consensus topology resulting from the Bayesian inference analysis. Nodal support is indicated at each node, except where the relationship received negligible support. Posterior probabilities (from the Bayesian inference analysis) and bootstrap values (from the maximum-likelihood analysis) are indicated before and after the slashes ("/") at branches of interest (i.e., nodal support for fairly shallow relationships within intraspecific haplogroups are omitted). The scale represents substitutions per site. For each terminal, country of origin and next-largest administrative unit (state, department, province, etc.) are provided (when reported by the team that generated them; see detailed voucher and locality information in supplementary file 1 for sequences that we generated). GenBank accession numbers are indicated for each terminal.
Figure 3 from: Gutiérrez EE, Helgen KM, McDonough MM, Bauer F, Hawkins MTR, Escobedo-Morales LA, Patterson BD, Maldonado JE (2017) A gene-tree test of the traditional taxonomy of American deer: the importance of voucher specimens, geographic data, and dense sampling. ZooKeys 697: 87-131. https://doi.org/10.3897/zookeys.697.15124
Figure 3 - Hind foot bones of Mazama rufina (A) and Pudu puda (B) sensu Hershkovitz (1982). According to Hershkovitz (1982; see also Brooke 1874, 1878), the union of the cuboideonavicular and external and middle cuneiform tarsal bones into a single bone in Pudu is the only osteological characteristic shared by P. puda and P. mephistophiles that consistently separates them from all other living deer, with exception of the genera Elaphodus and Muntiacus.
Figure 2 from: Gutiérrez EE, Helgen KM, McDonough MM, Bauer F, Hawkins MTR, Escobedo-Morales LA, Patterson BD, Maldonado JE (2017) A gene-tree test of the traditional taxonomy of American deer: the importance of voucher specimens, geographic data, and dense sampling. ZooKeys 697: 87-131. https://doi.org/10.3897/zookeys.697.15124
Figure 2 - Overall morphological appearance of "M." pandora (panels A–C) and that of the genus Odocoileus (panels D–F). Notice the grayish pelage and divergent antlers larger than in other species currently classified in Mazama. "M." pandora, panels A and C individuals kept in captivity at the Parque Zoológico del Bicentenario Animaya, Mérida, Yucatán, Mexico (photographs by Luis A. Escobedo-Morales)—provenance unknown; panel B individual kept in captivity in Tekax, Yucatán, Mexico (photograph by Rosa María González Marín)—provenance unknown. Odocoileus virginianus (see proposals by Molina and Molinari 1999 and Molinari 2007); panels D and E Monteredondo, Parque Nacional Chingaza, ca. 47 km (by road) E Bogota, Cundinamarca, Colombia (photographs by Aideé Vargas-Espinoza and Irene Aconcha, respectively); panel F Laguna de Mucubají, Parque Nacional Sierra Nevada, Mérida, Venezuela (photograph by Rodrigo Díaz Lupanow).
Figure 1a from: Gutiérrez EE, Helgen KM, McDonough MM, Bauer F, Hawkins MTR, Escobedo-Morales LA, Patterson BD, Maldonado JE (2017) A gene-tree test of the traditional taxonomy of American deer: the importance of voucher specimens, geographic data, and dense sampling. ZooKeys 697: 87-131. https://doi.org/10.3897/zookeys.697.15124
Figure 1a - Phylogenetic tree of cytochrome-b sequences of Odocoileini. This is a strict consensus topology resulting from the Bayesian inference analysis. Nodal support is indicated at each node, except where the relationship received negligible support. Posterior probabilities (from the Bayesian inference analysis) and bootstrap values (from the maximum-likelihood analysis) are indicated before and after the slashes ("/") at branches of interest (i.e., nodal support for fairly shallow relationships within intraspecific haplogroups are omitted). The scale represents substitutions per site. For each terminal, country of origin and next-largest administrative unit (state, department, province, etc.) are provided (when reported by the team that generated them; see detailed voucher and locality information in supplementary file 1 for sequences that we generated). GenBank accession numbers are indicated for each terminal.
Figure 2 from: López Berrizbeitia MF, Sánchez RT, Barquez RM, Díaz MM (2017) An update on the distribution and nomenclature of fleas (Order Siphonaptera) of bats (Order Chiroptera) and rodents (Order Rodentia) from La Rioja Province, Argentina. ZooKeys 678: 139-154. https://doi.org/10.3897/zookeys.678.12006
Figure 2 - Species of fleas representing the first record for La Rioja Province, Argentina. a Craneopsylla minerva, ♀ CMLA (608) (Stephanocircidae b Polygenis (Polygenis) acodontis, ♂ CMLA (674) (Rhopalopsyllidae) c Delostichus talis, ♀ CMLA (616) (Rhopalopsyllidae) d Delostichus talis, ♂ CMLA (619) (Rhopalopsyllidae) e Tiamastus palpalis, ♀ CMLA (631) (Rhopalopsyllidae) f Tiamastus palpalis, ♂ CMLA (629) (Rhopalopsyllidae). Scale=500 um.
Figure 1 from: López Berrizbeitia MF, Sánchez RT, Barquez RM, Díaz MM (2017) An update on the distribution and nomenclature of fleas (Order Siphonaptera) of bats (Order Chiroptera) and rodents (Order Rodentia) from La Rioja Province, Argentina. ZooKeys 678: 139-154. https://doi.org/10.3897/zookeys.678.12006
Figure 1 - Map illustrating the localities of fleas of bats and rodents from La Rioja Province, Argentina. The symbol with associated locality number are listed on map by latitude from north to south. The localities include specific locality, coordinates, department, and altitudes as follow: 1 700 m E of National Route 40 (28°24'17.4"S, 67°04'48.4"W), San Blas Department, 1123 m 2 Quebrada de Santo Domingo 30 km SW of Jagüé (28°31'34.7"S, 68°46'13.8"W), Vinchina Department, 3131 m 3 2 km S Río de La Punta on provincial road 7 (28°45'28.8"S; 66°47'09.3"W), Arauco Department, 996 m 4 Reserva Aguada de las Alturas, 4 km W Anillaco (28°47.942'S, 66°59.749'W), Castro Barros Department, 1188 m 5 Anillaco, 500 m W of plaza de Anillaco (28°48'40.30"S, 66°55'55.55"W), Castro Barros Department, 500 m 6 Anillaco 1.7 m E of CRILAR (28°48'46.00"S, 66°55'50.44"W), Castro Barros Department, 1357 m 7 Anillaco, behind cemetery (28°48'49.04"S, 66°56'0.75"W), Castro Barros Department, 1365 m 8 800 m E Anillaco (28°48.572' S; 66°55.193' W), Castro Barros Department, 780 m 9 Cuesta La Cébila, 22 km NW of Chumbicha, by route 60 (28°50'S, 66°24'W), Capital Department: 1066 m 10 5 km S of Cañón del Ocre (28°51'55.9"S, 67°41'26.3"W), Famatina Department, 2495 m 11 8 km NE of Cañón del Ocre, (28°57'37.3"S, 67°41'26.3"W), Famatina Department, 3127 m 12 Zapallar, (29°18'24.74"S, 68°40'9.2"W), Coronel Felipe Varela Department, 1634 m 13 1 km N Los Tambillos (29°22'S, 67°47'W), Coronel Felipe Varela Department, 1951 m 14 2 km E of Malanzán, camping El Descanso (30°48'37.7'"S, 66°34'40.3"W), General Facundo J. Quiroga Department, 957 m 15 Ulapes, 1 km W of plaza principal de Ulapes (31°34'35"S, 66°14'55"W), San Martín Department, 493 m.
Figure 1 from: Arbo MM (2017) Neotypification of Clytostoma sciuripabulum Hovel. PhytoKeys 78: 17-21. https://doi.org/10.3897/phytokeys.78.10649
Figure 1 - Clytostoma sciuripabulum Hovel. S15-37635, and S15-37634 (Neotype). Copyright of images: Naturhistoriska riksmuseet, Stockholm.
Figure 4 from: Gossner MM, Heckmann R, Moretti M (2018) From the South and from the North? – Quilnus marcosi Heiss & Baena and Aradus angularis J. Sahlberg, two flat bug species new for Central Europe (Hemiptera, Heteroptera, Aradidae). Alpine Entomology 2: 7-14. https://doi.org/10.3897/alpento.2.21801
Figure 4 Frequency of occurrences of Aradus angularis J. Sahlberg, 1886 with respect to time since fire (left) and elevation (right), based on previous records in Fennoscandia (grey) and the new record in Switzerland (red). Please note that data were available for a subset of records only.
Figure 1 from: Gossner MM, Heckmann R, Moretti M (2018) From the South and from the North? – Quilnus marcosi Heiss & Baena and Aradus angularis J. Sahlberg, two flat bug species new for Central Europe (Hemiptera, Heteroptera, Aradidae). Alpine Entomology 2: 7-14. https://doi.org/10.3897/alpento.2.21801
Figure 1 Photographs of the burnt site in Leuk, Valais, Switzerland: (A) Detail of the forest in 2003, one month after the fire; (B) Overview in August 2013 and (C) Detail of the site incl. Combi-trap in April 2013 (Aradus angularis J. Sahlberg, 1886 was sampled in June 2013); (D) Surrounding and (E) detail of the burnt pine tree (Pinus sylvestris) on which Quilnus marcosi Heiss & Baena, 2006 was detected in 2017 under one of a few remaining bark pieces. Photo credits: A: Marco Moretti, B, E: Beat Wermelinger, C: Martin Obrist, D: Martin M. Gossner.
Figure 3 from: Gossner MM, Heckmann R, Moretti M (2018) From the South and from the North? – Quilnus marcosi Heiss & Baena and Aradus angularis J. Sahlberg, two flat bug species new for Central Europe (Hemiptera, Heteroptera, Aradidae). Alpine Entomology 2: 7-14. https://doi.org/10.3897/alpento.2.21801
Figure 3 Records of Aradus angularis J. Sahlberg, 1886 (blue, n=46) and Quilnus marcosi Heiss & Baena, 2006 (red, n=7) in Europe, and new records of both species in Switzerland (star). Data are based on Heiss and Péricart (2007), Brustel (2009), Heiss (2010), Esser (Mallorca, unpubl., leg. Esser, det. coll. MMG) and the website of the Muséum national d'histoire naturelle Paris (https://science.mnhn.fr/institution/mnhn/collection/eh/item/eh18974?lang=en_US) for Q. marcosi and Reuter (1900), Helioevaara and Vaisanen (1983), Pettersson and Nilsson (1986), Lammes and Rinne (1990), Roth and Coulianos (2014), Hagglund et al. (2015), Heikkala et al. (2017), Heikkala (pers. com.), Martikainen (pers. com.), Artportalen Sveden (https://artfakta.artdatabanken.se/taxon/100379) and Kirishenko (1951) for A. angularis. Please note that data points in the European part of Russia represent the centre of each Oblast in which the species has been recorded.
Figure 2 from: Gossner MM, Heckmann R, Moretti M (2018) From the South and from the North? – Quilnus marcosi Heiss & Baena and Aradus angularis J. Sahlberg, two flat bug species new for Central Europe (Hemiptera, Heteroptera, Aradidae). Alpine Entomology 2: 7-14. https://doi.org/10.3897/alpento.2.21801
Figure 2 Two flat bug (Aradidae) species new to Central Europe, sampled in the burnt forest site in Leuk, Valais, Switzerland. (A) Male of Aradus angularis J. Sahlberg, 1886, sampled with a "Combi-trap" at 1730 m a.s.l. in June 2013 (sampling period 21 May to 23 June), leg. MM, det. coll. RH. Characteristic for the species are the size, the very thin antennae and the elongated body with the almost parallel outer margins of the wings and the form of the male genital structures. (B) Stenoptere male and juvenile of Quilnus marcosi Heiss & Baena, 2006, sampled under the bark of a burnt pine (Pinus sylvestris) tree at 1480 m a.s.l. on 1 June 2017, leg. det. coll. MMG. Characteristic for the species within the genus are the small size, the rounded apical corners of the pronotum and the form of the male genital structures. Photo credits: Gerhard Strauß.
Figure 3 from: Al-Mahadeen MM, Jaber AM, Al-Najjar BO (2024) Design, synthesis and biological evaluation of novel 2-hydroxy-1 H-indene-1,3(2 H)-dione derivatives as FGFR1 inhibitors. Pharmacia 71: 1-9. https://doi.org/10.3897/pharmacia.71.e122127
Figure 3 Stick representation of a. Erdafitinib; b. 7b; c. 9a; d. 9b; e. 9c in grey colour, docked within FGFR1 (PDB ID: 5EW8) binding site (green). Generated by Biovia Discovery Studio visualizer®.
Figure 2 from: Al-Mahadeen MM, Jaber AM, Al-Najjar BO (2024) Design, synthesis and biological evaluation of novel 2-hydroxy-1 H-indene-1,3(2 H)-dione derivatives as FGFR1 inhibitors. Pharmacia 71: 1-9. https://doi.org/10.3897/pharmacia.71.e122127
Figure 2 Solid ribbon representation of FGFR1 (PDB ID: 5EW8) with co-crystal (grey) and re-docked (orange) erdafitinib. Generated by Biovia Discovery Studio visualizer®.
Figure 4 from: Al-Mahadeen MM, Jaber AM, Al-Najjar BO (2024) Design, synthesis and biological evaluation of novel 2-hydroxy-1 H-indene-1,3(2 H)-dione derivatives as FGFR1 inhibitors. Pharmacia 71: 1-9. https://doi.org/10.3897/pharmacia.71.e122127
Figure 4 Dose-response curves of compounds 7b, 9a, 9b and 9c FGFR1 inhibitor. A. Dose-response curve of 7b with IC50 = 3.1 μM; B. Dose-response curve of 9a with IC50 = 5.7 μM; C. Dose-response curve of 9b with IC50 = 3.3 μM; D. Dose-response curve of 9c with IC50 = 4.1 μM.
Рис. 21–22. Coelorinchus idiolepis sp. nov., гоΛотип (21) и C. anisacanthus, гоΛотип (22), чешуйный покров поΔ основанием первого спинного пΛавника выше боковой Λинии. Масштаб: 21 — 15 мм; 22 — 10 мм Figs. 21–22. Coelorinchus idiolepis sp. nov., holotype (21) and C. anisacanthus, holotype (22), squamation below first dorsal-fin base and above lateral line. Scale bars: 21 — 15 mm; 22 — 10 mm in Coelorinchus From The Hawaiian-Emperor Seamount Chain (The Pacific Ocean) (Teleostei, Gadiformes, Macrouridae)
Рис. 21–22. Coelorinchus idiolepis sp. nov., гоΛотип (21) и C. anisacanthus, гоΛотип (22), чешуйный покров поΔ основанием первого спинного пΛавника выше боковой Λинии. Масштаб: 21 — 15 мм; 22 — 10 мм Figs. 21–22. Coelorinchus idiolepis sp. nov., holotype (21) and C. anisacanthus, holotype (22), squamation below first dorsal-fin base and above lateral line. Scale bars: 21 — 15 mm; 22 — 10 mm
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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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.