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opencc-by-4.0Oct 2020View details →

Figure 3 in The global freshwater bivalve checklist's extension: Freshwater occurrences and phylogenetic position of Galatea clams from West Africa (Venerida: Donacidae)

Figure 3. Shells of Galatea schwabi from Sanaga River, Cameroon. (A-B) Topotypes RMBH biv800, Mouanko (lower reaches, slightly brackish section). (C-D) Specimens RMBH biv801, Monatélé (middle reaches, freshwater section). Red arrows show well-developed muscle attachment scars. Scale bar = 10 mm. (Photos: Artem A. Lyubas).

opencc-by-4.0Oct 2020View details →

Figure 5 in The global freshwater bivalve checklist's extension: Freshwater occurrences and phylogenetic position of Galatea clams from West Africa (Venerida: Donacidae)

Figure 5. Maximum likelihood (IQ-TREE) phylogeny of Bivalvia (Venerida and Adapedonta) based on the COI gene sequences (Table 1). A Galatea member is dark red. Scale bar indicates the branch lengths (substitutions per site). Black numbers near nodes indicate the ultrafast bootstrap support (BS) values.

opencc-by-4.0Oct 2020View details →

Figure 1 in The global freshwater bivalve checklist's extension: Freshwater occurrences and phylogenetic position of Galatea clams from West Africa (Venerida: Donacidae)

Figure 1. Occurrences of Galatea schwabi (red stars) and Galatea paradoxa (light green stars). The locality data is given in Table 2. Freshwater basins are colored as follows: Sanaga (1), Cross (2), Niger (3), and Volta (4). The red dash indicates the Edea Hydroelectric Power Station's dam on the Sanaga River. (Map: Mikhail Y. Gofarov).

opencc-by-4.0Jun 2023View details →

Figures 1–8 in On the systematic position of the genus Proaegeria Le Cerf 1916 (Lepidoptera: Sesiidae) with description of a new species

Figures 1–8. Moths. Proaegeria murzini sp. n.: 1–2. Holotype, male, Sesiidae pictures №№ 0023-0024–2023; 3–4. Paratype, male. Sesiidae pictures №№ 0021-0022–2023; 5–6. Paratype, male. Sesiidae pictures №№ 0025-0026–2023; 7–8. Paratype, female. Sesiidae pictures №№ 0019-0020–2023. Dorsal view (1, 3, 5, 7) and ventral view (2, 4, 6, 8).

opencc-by-4.0Jun 2023View details →

Figures 9–14 in On the systematic position of the genus Proaegeria Le Cerf 1916 (Lepidoptera: Sesiidae) with description of a new species

Figures 9–14. Genitalia. Proaegeria murzini sp. n.: 9–14. Paratype, male, genitalia preparation № 010–2023. 9. Tegumen-uncus complex; 10. Valva; 11. Saccus; 12. Juxta, ventral view; 13. Phallus. 14. Paratype, female, genitalia preparation № 011–2023. Scale bar 1.0 mm.

Fig. 6 in Glanidium botocudo, a new species from the rio Doce and rio Mucuri, Minas Gerais, Brazil (Siluriformes: Auchenipteridae) with comments on taxonomic position of Glanidium bockmanni Sarmento-Soares & Buckup

Fig. 6. Map of eastern Brazilian drainages at northeastern Minas Gerais State illustrating regional uplifts: the Serra do Espinhaço (colored in dark gray) and Dom Silvério Group (colored in brown). Contour of river basins in the area as stated: rio São Francisco (in pink), rio Jequitinhonha (in rose), rio Mucuri (in light gray), rio Doce (in salmon). Collecting localities of Glanidium botocudo illustrated as black circles. Star indicates type locality. Regional centromochlin species at rio São Francisco basin are illustrated by squares (white - Glanidium albescens; black - Centromochlus bockmanni). Congener at southern coastal rivers of Espírito Santo, Glanidium melanopterum, is illustrated by white lozenges. Symbols may represent more than one locality. Limits of Serra do Espinhaço are based on Valadão (2009) and Dom Silvério Group based on Peres et al. (2004).

Fig. 2 in Glanidium botocudo, a new species from the rio Doce and rio Mucuri, Minas Gerais, Brazil (Siluriformes: Auchenipteridae) with comments on taxonomic position of Glanidium bockmanni Sarmento-Soares & Buckup

Fig. 2. Neurocranium of Glanidium botocudo, MNRJ 32539, paratype, 82.0 mm SL. Dorsal view. Abbreviations: ep, epioccipital; fo, cranial fontanel, fr, frontal; le, lateral ethmoid; me, mesethmoid; na, nasal; n1, first nuchal plate, n2; second nuchal plate; n3, third nuchal plate; pe, posterior epioccipital process; ps, posttemporal-supracleitrum; pt, pterotic; so, supraoccipital; sp, sphenotic. Scale bar = 1.0 mm.

Fig. 1 in Glanidium botocudo, a new species from the rio Doce and rio Mucuri, Minas Gerais, Brazil (Siluriformes: Auchenipteridae) with comments on taxonomic position of Glanidium bockmanni Sarmento-Soares & Buckup

Fig. 1. Glanidium botocudo, new species, (a) holotype, MNRJ 32538, male, 93.2 mm SL, rio Mucuri downstream from Santa Clara Dam, Nanuque, Minas Gerais State, Brazil. (b) paratype, MBML 2047, female, 86.8 mm SL, rio Doce, on area of influence of Baú I Dam, Santa Cruz do Escalvado, Minas Gerais State, Brazil.

Fig. 4 in Glanidium botocudo, a new species from the rio Doce and rio Mucuri, Minas Gerais, Brazil (Siluriformes: Auchenipteridae) with comments on taxonomic position of Glanidium bockmanni Sarmento-Soares & Buckup

Fig. 4. Right hyoid arch of Glanidium botocudo, MNRJ 32539, paratype, 82.0 mm SL. Ventral view. Abbreviations: ac, anterior ceratohyal; br, branchiostegal rays; dh, dorsal hypohyal; ic, interceratohyal cartilage; ih, interhyal; pc, posterior ceratohyal; vh, ventral hypohyal; uh, urohyal; up, urohyal ventral process. Scale bar = 1.0 mm.

Fig. 3 in Glanidium botocudo, a new species from the rio Doce and rio Mucuri, Minas Gerais, Brazil (Siluriformes: Auchenipteridae) with comments on taxonomic position of Glanidium bockmanni Sarmento-Soares & Buckup

Fig. 3. Right suspensorium of Glanidium botocudo, MNRJ 32539, paratype, 82.0 mm SL. Lateral view. Abbreviations: aa, angulo-articular; dn, dentary; hy, hyomandibula; io, interopercle; mt, metapterygoid; ms, mesopterygoid; op, opercle; po, preopercle; qu, quadrate; sb, subpreopercle; sp, suprapreopercle. Scale bar = 1.0 mm.

opencc-by-4.0Aug 2024View details →

Unravelling the Dependence of Aptamer–Target Binding Orientation and Strength on Nucleotide Modification Size, Position, and Number: A Computational Case Study of TBA

<p>Data deposition for "Unravelling the Dependence of Aptamer–Target Binding Orientation and Strength on Nucleotide Modification Size, Position, and Number: A Computational Case Study of TBA" published in Nucleic Acids Research. Data includes custom paramaterized nucleobase residues for use in AMBER molecular dyanmics simulations. Initial structures and setup code along with starting structures for generation of simulations in AMBER (pmemd.cuda). A in-house "MD-Generator" script to create nessessary files with our select simulation settings. Lastly, also included are CPPTRAJ analysis commands and scripts with visualizion scripts for use in Pymol 2.5 and above. </p>

opencc-by-4.0Dec 2013View details →

Figure 1 in Strategies for false positive reduction and multimodal lesion characterization in computer-aided diagnosis of breast cancer

Figure 1. - Representative ultrasound images at four-month post copulation (8 Sep. 2010) before resorption, five-month post copulation (20 Oct. 2010) during resorption, and six-month post copulation (3 Nov. 2010) after resorption. A: Uterine horn; B: Fetus; C: Ovary; D: Follicle.

opencc-by-4.0Apr 2021View details →

Fig. 2 in Plague transforms positive effects of precipitation on prairie dogs to negative effects

Fig. 2. Relationship between visual count changes in prairie dogs (Cynomys spp.) and annual precipitation (cm) on plots without plague management and with plague management by treating burrows with deltamethrin dust for flea control. Population change (λ) was indexed by visual counts conducted in mid-summer of adults plus juveniles, and annual precipitation was cumulative during the 12-month period prior to the typical date of the second count (interval of 1 July-30 June). Visual counts are presented as treated in the analysis (re-scaled λ, natural log transformed), although the repeated measures analysis retained the pairings of treatments that cannot be illustrated here. Points above the dashed line indicate population increases; points below the dashed line indicate population declines with points on the zero-line indicating population collapse to 0 animals.

opencc-by-4.0Apr 2021View details →

Fig. 1 in Plague transforms positive effects of precipitation on prairie dogs to negative effects

Fig. 1. Study sites in the western United States where the influence of precipitation on prairie dog population change was evaluated on paired plots with and without deltamethrin treatment to control the flea vectors of plague. Prairie dog sketch by D. Crawford.

Fig. 9 in New sauropodomorph and cynodont remains from the Late Triassic Sacisaurus site in southern Brazil and its stratigraphic position in the Norian Caturrita Formation

Fig. 9. Traversodontidae indet. (cf. Exaeretodon sp.) from Sacisaurus site, Late Triassic Caturrita Formation, Agudo, Rio Grande do Sul Brazil; MCN-PV 10205, isolated left lower incisor 1 in lingual (A) and distal (B) views.

Fig. 8. A in New sauropodomorph and cynodont remains from the Late Triassic Sacisaurus site in southern Brazil and its stratigraphic position in the Norian Caturrita Formation

Fig. 8. A. Probainognathian cynodonts from Sacisaurus site, Late Triassic Caturrita Formation, Agudo, Rio grande do Sul, Brazil; isolated left lower postcanine tooth (MCN-PV 10204) originally interpreted as belonging to Riograndia, in labial (A1) and lingual (A2) views. B, C. Riograndia guaibensis Bonaparte, Ferigolo, and Ribeiro, 2001 from the Riograndia Assemblage Zone, Linha São Luiz site, Late Triassic Caturrita Formation, Faxinal do Soturno, Rio grande do Sul, Brazil; anterior postcanines of UFRGS-PV-833-T in lingual view (B) and UFRGS-PV-1319-T in labial view (C). D, E. Riograndia guaibensis from Sacisaurus site, Late Triassic Caturrita Formation, Agudo, Rio grande do Sul, Brazil, originally referred to Brasilitherium riograndensis; isolated right lower postcanines of MCN-PV 10102 (D) and MCN-PV 10103 (E), in labial (D1, E1) and lingual (D2, E2) views. F. Brasilodon quadrangularis Bonaparte, Martinelli, Schultz, and Rubert, 2003 from the Riograndia Assemblage Zone, Late Triassic Caturrita Formation, Faxinal do Soturno, Rio grande do Sul, Brazil, UFRGS-PV-603-T (inverted), detail of middle and posterior left lower postcanines, in labial (F1) and lingual (F2) views. Abbreviations: 4o, fourth cusp; 8o, eighth cusp; a–d, names of lower cusps; (e), cusp e; g, lower cusp g; cr, constriction; pc1, pc4, postcanine tooth 1 and 4.

Fig. 2 in New sauropodomorph and cynodont remains from the Late Triassic Sacisaurus site in southern Brazil and its stratigraphic position in the Norian Caturrita Formation

Fig. 2. Right ectopterygoid of a sauropodomorph from Sacisaurus site, Late Triassic Caturrita Formation, Agudo, Rio Grande do Sul, Brazil; MCN PV 10049 in dorsal (A) and ventral (B) views. Arrows point to cranial.

Fig. 7 in New sauropodomorph and cynodont remains from the Late Triassic Sacisaurus site in southern Brazil and its stratigraphic position in the Norian Caturrita Formation

Fig. 7. Distal end of metatarsal I of a sauropodomorph from Sacisaurus site, Late Triassic Caturrita Formation, Agudo, Rio Grande do Sul, Brazil; MCN PV 10049 in cranial (A), lateral (B), caudal (C), mediodistal (D), and distal (E) views.

Fig. 5 in New sauropodomorph and cynodont remains from the Late Triassic Sacisaurus site in southern Brazil and its stratigraphic position in the Norian Caturrita Formation

Fig. 5. Left femur of a sauropodomorph from Sacisaurus site, Late Triassic Caturrita Formation, Agudo, Rio Grande do Sul, Brazil; MCN PV10008 in medial (A), cranial (B), lateral (C), and caudal (D) views. The head fragment in articulation with the rest of the bone in craniolateral (E) and caudomedial (F) views. Abbreviation: M., muscle.

Fig. 10 in New sauropodomorph and cynodont remains from the Late Triassic Sacisaurus site in southern Brazil and its stratigraphic position in the Norian Caturrita Formation

Fig. 10. Strict consensus tree of 2052 MPTs found in the analysis of the data matrix of Bronzati et al. (2018), showing the phylogenetic relationships of MCN PV sauropodomorph among Triassic sauropodomorphs and other dinosauromorphs.