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Fig. 2. Statistical parsimony cladogram network representing relationships among the 45 haplotypes for a 615 in Genetic diversity of Halyomorpha halys (Hemiptera, Pentatomidae) in Korea and comparison with COI sequence datasets from East Asia, Europe, and North America
Fig. 2. Statistical parsimony cladogram network representing relationships among the 45 haplotypes for a 615 bp fragment of the COI gene of Halyomorpha halys. Each circle is labeled with haplotype number, and the size of each circle is proportional to the frequency of each haplotype [H3 (n = 353); H1 (n = 285); H22 (n = 43); H8 (n = 34); H33 (n = 23); H2 (n = 16); H32 (n = 8); H7, H9–H13, and H43 (n = 3); H6, H14, H34, H39, and H40 (n = 2); H4–H5, H12, H15–H21, H23, H30–H31, H35–H38, H41, H42, and H44–H51 (n = 1)]. Differing colors indicate countries in which samples were collected.
Fig. 5 in Range expansion of the invasive Tropical House Gecko, Hemidactylus mabouia (Squamata: Gekkonidae), in South America
Fig. 5. Known distribution of Hemidactylus mabouia in South America. Black circles represent literature data (most previous records) and red circles indicate the location of new records in Peru (2008–2019). Other relatively recent records in Peru (1989– 1999) are from the San Martin and Huánuco regions (yellow triangle and square). Recent records from coastal Ecuador are indicated with yellow diamonds. The color scheme of the map represents the elevation in m asl (see legend on the right).
Fig. 4. A in Range expansion of the invasive Tropical House Gecko, Hemidactylus mabouia (Squamata: Gekkonidae), in South America
Fig. 4. A consensus Bayesian phylogeny based on 474 bp of aligned mitochondrial sequences (16s rRNA gene). Posterior probability values are shown on nodes. The arrow indicates the specimen from central Peru (MUSM 33241; Field Nbr. RvM64–14).
Fig. 1 in Range expansion of the invasive Tropical House Gecko, Hemidactylus mabouia (Squamata: Gekkonidae), in South America
Fig. 1. Dorsal views of head (A), midbody (B), and tail (C) of adult female of Hemidactylus mabouia (MUSM 33241; Field Nbr. RvM64–14) collected in Chanchamayo, Peru. Dorsal views of head (D), midbody (E), and tail (F) of adult female Hemidactylus frenatus (MVZ 73664) collected in Bataan Province, Philippines. Photographs by Rudolf von May.
Fig. 2 in Range expansion of the invasive Tropical House Gecko, Hemidactylus mabouia (Squamata: Gekkonidae), in South America
Fig. 2. Dorsal views of adult male Hemidactylus mabouia (CORBIDI 6276) collected in Loreto (Genaro Herrera, Requena Province), Peru (A). Dorsal view of juvenile Hemidactylus mabouia (CORBIDI 15363) collected in Lima (Surquillo, Lima Province), Peru (B). Lateral view of body (C) and head (D), ventral view of head and body (E), and ventral view of right hand (F) of the same individual (CORBIDI 15363). Photographs by Pablo Venegas (A) and Germán Chávez (B–F).
Fig. 3 in Range expansion of the invasive Tropical House Gecko, Hemidactylus mabouia (Squamata: Gekkonidae), in South America
Fig. 3. Dorsolateral views of adult Hemidactylus frenatus from Aur Island, Malaysia (A), Nam Du Island, Vietnam (B), and Villavicencio, Meta, Colombia (C–D). Photographs by L. Lee Grismer (A–B) and Juan D. Vásquez-Restrepo (C–D).
Figs 11-15 in A new species of velvet mite from meridional South America of the genus Clavismaris (Acari, Erythraeoidea, Smarididae, Hirstiosomatinae)
Figs 11-15. Clavismaris maquine sp. nov. Figs 11, 14, 15, female ♀ (MCN ARA 1912); Figs 12, 13, ♀ (MCN ARA 1915): 11, dorsal scutum (only base of sensillary setae indicated); 12, genital opening; 13, anal opening; 14, anterior sensillary area; 15, posterior sensilary area (asa, anterior sensillary area; as, anterior sensilla; e, eye; psa, posterior sensillary area; ps, posterior sensilla). Scale bars: Figs 11, 12, 14, 15, 100 μm; Fig. 13, 50μm.
Figs 6-10 in A new species of velvet mite from meridional South America of the genus Clavismaris (Acari, Erythraeoidea, Smarididae, Hirstiosomatinae)
Figs 6-10. Clavismaris maquine sp. nov. Female holotype ♀ (MCN ARA 1912): 6, eye region and surrounding scobalae. Paratype ♂ (MCN ARA 1913): 7, idiosoma, ventral view; 8-10, genital sclerite in ventral view, respectively from distal plan to proximal plan of view (e, eye; mgs, male genital sclerite; psa, posterior sensillary area). Scale bars: Fig. 6, 50 μm; Fig. 7, 500μm; Figs 8-10, 200 μm.
Figs 1-5 in A new species of velvet mite from meridional South America of the genus Clavismaris (Acari, Erythraeoidea, Smarididae, Hirstiosomatinae)
Figs 1-5. Clavismaris maquine sp. nov., holotype ♀ (MCN ARA 1912): 1, body, dorsal; 2, gnathosoma and propodossoma, dorsal; 3, tarsi, legs I, lateral; 4, tarsus, leg IV, lateral; 5, genital region, dorsal. Scale bars: Fig. 1, 500 μm; Figs 2, 3, 200 μm; Figs 4, 5, 100 μm.
Fig. 3. Crassatelline bivalves from Central and South America. A, B in Fossil Cenozoic crassatelline bivalves from Peru: New species and generic insights
Fig. 3. Crassatelline bivalves from Central and South America. A, B. Kalolophus antillarum (Reeve, 1842). A. UWBM 101885, Recent, Pacific coast of Panama; exterior (A1) and interior (A2) of left valve. B. UWBM 101884, Recent, Venezuela; dorsal view of paired valves, anterior at right. C. Hybolophus berryi (Spieker, 1922), USNM 562399, early Miocene, lower Zorritos Formation, Zorritos, Peru; exterior of left valve (C1), dorsal view of paired valves C2), anterior at right. D. Hybolophus elassa Woodring, 1982, USNM 647424, late Miocene, Gatun Formation, Panama; exterior of left valve. E. Kalolophus mediamaricanus (Brown and Pilsbry, 1913), USNM 647421, early Miocene, La Boca Formation, Panama; exterior of right valve. F. Kalolophus sp., USNM 647423, late Miocene, middle Gatun Formation, Panama; exterior (F1) and interior (F2) of left valve. G. Kalolophus jamaicensis (Dall, 1903), USNM 135683, Pliocene, Bowden Formation, Jamaica; interior of left valve. H. Kalolophus speciosus (Adams, 1854), SBMNH 140817, Recent, Panama City, Florida; exterior (H1) and interior (H2) of left valve; dorsal view of paired valves (H3), anterior at right. Scale bars 10 mm.
Fig. 16. Conodont P1 in Geometric morphometric analysis and taxonomic revision of the Gzhelian (Late Pennsylvanian) conodont Idiognathodus simulator from North America
Fig. 16. Conodont P1 elements of Idiognathodus luganicus (Kozitskaya, 1978) from the Heebner Shale (Gzhelian, Late Pennsylvanian). A. SUI 141094 TT0200); Sedan 11. B. SUI 141095 (TT0209); Clinton 12. C. SUI 141098 (TT0285); Clinton 12. D. SUI 141096 (TT0284); Clinton 12. E. SUI 141097 TT0141); Clinton 28. F. SUI 141099 (TT0018); Clinton 15. G. SUI 141100 (TT0026); I229-83. H. SUI14101 (TT0016); Clinton 14. I. SUI 14102 TT0119); Sedan 20. J. SUI 141103 (TT0118); Sedan 20. K. SUI 141104 (TT0102); Sedan 12.
Fig. 15. Conodont P1 in Geometric morphometric analysis and taxonomic revision of the Gzhelian (Late Pennsylvanian) conodont Idiognathodus simulator from North America
Fig. 15. Conodont P1 elements of Idiognathodus lateralis sp. nov. (A–M) and Idiognathodus praenuntius (Chernykh, 2005) (N–T) from the Heebner Shale, Gzhelian (Late Pennsylvanian). A. SUI 141062 (TT0228); Sedan 11. B. SUI 141063 (TT0233); Sedan 11. C. SUI 141064 (TT0050); Clinton 20. D., SUI 141065 (TT0019); Clinton 22. E. SUI 141066 (TT0168); Sedan 23. F. SUI 141067 (TT0261); Sedan 11. G. SUI 141068 (TT0260); Sedan 11. →
Fig. 14. Conodont P1 in Geometric morphometric analysis and taxonomic revision of the Gzhelian (Late Pennsylvanian) conodont Idiognathodus simulator from North America
Fig. 14. Conodont P1 elements of Idiognathodus auritus (Chernykh, 2005) from the Heebner Shale, Gzhelian (Late Pennsylvanian). A. SUI 141042 (TT0314); Sedan 17. B. SUI 141043 (TT0311); Sedan 24. C. SUI 141044 (TT0251); Sedan 11. D. SUI 141045 (TT0222); Clinton 12. E. SUI 141046 (TT0251); Sedan 11. F. SUI 141047 (TT0235); Sedan 11. G. SUI 141048 (TT0256); Sedan 11. H. SUI 141049 (TT0095); I229-83. I. SUI 141050 (TT0093); Clinton 21. J . SUI 141051 (TT0094); I229-83. K. SUI 141052 (TT0221); Clinton 12. L. SUI 141053 (TT0169); Sedan 23. M. SUI 141054 (TT0167); Sedan 23.
Fig. 12 in Geometric morphometric analysis and taxonomic revision of the Gzhelian (Late Pennsylvanian) conodont Idiognathodus simulator from North America
Fig. 12. Canonical variation (CV) cross-plots and wireframes for all grooved sinistral (A) and dextral (B) elements, using locality (red, Clinton; green, I-229; blue, Sedan) as the group-defining criterion. Gray wireframes, mean form provided by the preliminary Procrustes fit; black wireframes, form achieved with values of the corresponding canonical variate.
Fig. 11 in Geometric morphometric analysis and taxonomic revision of the Gzhelian (Late Pennsylvanian) conodont Idiognathodus simulator from North America
Fig. 11. Cross-plot of morphotype membership for each grooved sinistral (A) and dextral (B) specimen on the x-axis and their centroid size along the y-axis. Centroid size is not a measure of length, because the outwards movement of any landmark from the centroid will cause it to increase, but for the sake of providing reference, specimens with a platform length less than 0.4 mm generally had a centroid size below 900.
Fig. 8 in Geometric morphometric analysis and taxonomic revision of the Gzhelian (Late Pennsylvanian) conodont Idiognathodus simulator from North America
Fig. 8. Cross-plot of the first two principal components (labeled with their corresponding eigenvalues) and wireframes (A) and canonical variation plot (using chirality membership as the group defining criterion) and wireframes (B) for Idiognathodus luganicus. Black wireframes, form with values of the corresponding principal component values; gray wireframes, mean form provided by the preliminary Procrustes fit; blue/red wireframes, form achieved with values of the corresponding canonical variate; blue, sinistral; red, dextral.
Fig. 10 in Geometric morphometric analysis and taxonomic revision of the Gzhelian (Late Pennsylvanian) conodont Idiognathodus simulator from North America
Fig. 10. Principal component cross-plots of the first two principal components (labeled with their corresponding eigenvalues) and wireframes (A, B) and canonical variation plots (using chirality membership as the group defining criterion) and wireframes (C, D) for Idiognathodus simulator (A, C) and Idiognathodus auritus (B, D). Black wireframes, form with values of the corresponding principal component values; gray wireframes, mean form provided by the preliminary Procrustes fit; blue/red wireframes, form achieved with values of the corresponding canonical variate; blue, sinistral; red, dextral.
Fig. 6 in Geometric morphometric analysis and taxonomic revision of the Gzhelian (Late Pennsylvanian) conodont Idiognathodus simulator from North America
Fig. 6. Canonical variation plot and wireframes for all grooved specimens, using chirality membership as the group-defining criterion. Gray wireframe, the mean form provided by the preliminary Procrustes fit, and blue/ red wireframes, form achieved with values of the corresponding canonical variate; blue, sinistral; red dextral.
Fig. 7 in Geometric morphometric analysis and taxonomic revision of the Gzhelian (Late Pennsylvanian) conodont Idiognathodus simulator from North America
Fig. 7. Canonical variation (CV) cross-plots and wireframes for all grooved sinistral (A) and dextral (B) elements, using lobe membership (red, 0 lobes; blue, 1 lobe; green, 2 lobes; purple, dicconnected ridge) as the group-defining criterion. Gray wireframes, mean form provided by the preliminary Procrustes fit; black wireframes, form achieved with values of the corresponding canonical variate.
Fig. 9 in Geometric morphometric analysis and taxonomic revision of the Gzhelian (Late Pennsylvanian) conodont Idiognathodus simulator from North America
Fig. 9. Principal component cross-plots of the first two principal components (labeled with their corresponding eigenvalues) and wireframes (A, B) and canonical variation plots (using chirality membership as the group defining criterion) and wireframes (C, D) for Idiognathodus lateralis (A, C) and Idiognathodus praenuntius (B, D). Black wireframes, form with values of the corresponding principal component values; gray wireframes, mean form provided by the preliminary Procrustes fit; blue/red wireframes, form achieved with values of the corresponding canonical variate; blue, sinistral; red, dextral.
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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.