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FIGURES 1–6 in Critical analysis of the type material of Mutillidae described from the Australasian Region (Hymenoptera)
FIGURES 1–6. Type (and non-type) specimens of Australasian Mutillidae. 1. Mutilla abdominalis Westwood, 1843, ♂, nontype specimens det. D.J. Brothers: habitus dorsal view, habitus lateral view. 2. Mutilla abjecta André, 1902, ♀, lectotype: habitus dorsal view, labels. 3. Mutilla aciculata Kohl, 1883, ♀, holotype: habitus dorsal view, metasoma dorsal view, labels. 4. Mutilla addenda André, 1902, ♀, holotype: habitus dorsal view, labels. 5. Mutilla adjacens André, 1902, ♂, holotype: habitus dorsal view, habitus lateral view, labels. 6. Ephutomorpha adjuncta André, 1903, ♀, lectotype: habitus dorsal view, labels.
FIGURE 8. Type specimens and label data. A in Korean species of the Atheta Thomson subgenus Dimetrota Mulsant & Rey (Coleoptera: Staphylinidae: Aleocharinae) with a description of new species
FIGURE 8. Type specimens and label data. A: lectotype of Atheta (Dimetrota) altaica; B: syntype of A. (D.) sublaevana [= A. (D.) atramentaria]; C: holotype of A. (D.) sulputrida [= A. (D.) atramentaria]; D: lectotype of A. (D.) furtiva; E: holotype of A. (D.) machonryongica; F: holotype of A. (D.) photaechonica; G: lectotype of A. (D.) subsericans; H: syntype of A. (Dimetrota) weisei; I: holotype of A. (D.) chagangensis = A. (Badura) tokiokai.
Distribution. NW Argentina (Catamarca), known only from the type locality, Sierra de Ambato, about 18 km NNW Chumbicha. in Abrocomidae
Distribution. NW Argentina (Catamarca), known only from the type locality, Sierra de Ambato, about 18 km NNW Chumbicha.
Distribution. NW Argentina (NW Rioja), known only from the Sierra de Famatina, the type series was from 35 km N of Nevado de Famatina Mt. in Abrocomidae
Distribution. NW Argentina (NW Rioja), known only from the Sierra de Famatina, the type series was from 35 km N of Nevado de Famatina Mt.
Distribution. CW Argentina (N Neuquén Province), known only from the type locality and neighboring areas in the Chos Malal Department. in Ctenomyidae
Distribution. CW Argentina (N Neuquén Province), known only from the type locality and neighboring areas in the Chos Malal Department.
Distribution. NW Argentina (SW Catamarca Province), known only from the vicinity ofthe type locality. in Ctenomyidae
Distribution. NW Argentina (SW Catamarca Province), known only from the vicinity ofthe type locality.
Distribution. NW Argentina (La Rioja Province), occurs at the type locality and probably nearby areas, in Sierra de Famatina, reaching elevations up to 3800 m. in Ctenomyidae
Distribution. NW Argentina (La Rioja Province), occurs at the type locality and probably nearby areas, in Sierra de Famatina, reaching elevations up to 3800 m.
Distribution. NW Argentina (N Tucuman Province), known only from the type locality and neighboring areas. in Ctenomyidae
Distribution. NW Argentina (N Tucuman Province), known only from the type locality and neighboring areas.
Distribution. CS Bolivia, known only from the type locality at Cerro Itahuaticua at 800-1800 m altitude. in Ctenomyidae
Distribution. CS Bolivia, known only from the type locality at Cerro Itahuaticua at 800-1800 m altitude.
Distribution. SW Brazil, known only from two sites, the type locality in Rondonia and Juruena (Mato Grosso State)Descriptive notes Head-body ¢.230 mm, tail ¢.80 mm. No specific data are available for body weight. Rondon's Tuco-tuco is medium-sized. Dorsal hairs are pale at bases and sepia at tips. Head and venterare slightly rufous, and tail is uniform brown. Skull is robust and depressed. Inter-maxillaries are also robust, with lateral protruding expansion; maxillaries are narrow; and mandible is strong and wide. Supraorbital process protrudes, and traverse occipital-temporal crest is straight. Bullae are inflated. in Ctenomyidae
Distribution. SW Brazil, known only from two sites, the type locality in Rondonia and Juruena (Mato Grosso State)Descriptive notes Head-body ¢.230 mm, tail ¢.80 mm. No specific data are available for body weight. Rondon's Tuco-tuco is medium-sized. Dorsal hairs are pale at bases and sepia at tips. Head and venterare slightly rufous, and tail is uniform brown. Skull is robust and depressed. Inter-maxillaries are also robust, with lateral protruding expansion; maxillaries are narrow; and mandible is strong and wide. Supraorbital process protrudes, and traverse occipital-temporal crest is straight. Bullae are inflated.
Evaluating the role of body size and habitat type in movement behavior in human-dominated systems: A frog's eye view
<p>Animal movement is a key process that connects and maintains populations on the landscape, yet for most species we do not understand how intrinsic and extrinsic factors interact to influence individual movement behavior. </p> <p>Land-use/land-cover changes highlight that connectivity among populations will depend upon an individual's ability to traverse habitats, which may vary as a result of habitat permeability, individual condition, or a combination of these factors.</p> <p>We examined the effects of intrinsic (body size) and extrinsic (habitat type) factors on desiccation tolerance, movement, and orientation in three anuran species (American toads, <em>Anaxyrus americanus</em>; northern leopard frogs, <em>Lithobates pipiens</em>; and Blanchard's cricket frogs, <em>Acris blanchardi</em>) using laboratory and field studies to connect the effects of susceptibility to desiccation, size, and movement behavior in single habitat types and at habitat edges.</p> <p>Smaller anurans were more vulnerable to desiccation, particularly for species that metamorphose at relatively small sizes. Habitat type had the strongest effect on movement, while body size had more situational and species-specific effects on movement. We found that individuals moved the farthest in habitat types that, when given the choice, they oriented away from, suggesting that these habitats are less favorable and could represent barriers for movement.</p> <p>Overall, our work demonstrated that differences in habitat type had strong impacts on individual movement behavior and influenced choices at habitat edges. By integrating intrinsic and extrinsic factors into our study, we provided evidence that population connectivity may be influenced not only by the habitat matrix, but the condition of the individuals leaving the habitat patch.</p>
Data and results from: "De novo spatiotemporal modelling of cell-type signatures in the developmental human heart"
<p>This repository contains data used and results produced in the manuscript:</p> <p>Sergio Marco Salas, Xiao Yuan, Christer Sylven, Mats Nilsson, Carolina Wählby, Gabriele Partel. "De novo spatiotemporal modelling of cell-type signatures in the developmental human heart"</p> <p>In situ sequencing [1] and scRNA-seq data [2] generated by Asp et al. [3] were downloaded and redistributed under CC BY 4.0 license.</p> <p>[1] Wu, Chenglin; Qian, Xiaoyan; Nilsson, Mats (2019): ISS data in "A spatiotemporal organ-wide gene expression and cell atlas of the developing human heart". figshare. Dataset. https://doi.org/10.6084/m9.figshare.10058048.v1 </p> <p>[2] Asp, Michaela (2021), “Developmental heart - filtered and unfiltered count matrices and meta tables”, Mendeley Data, V2, doi: 10.17632/mbvhhf8m62.2</p> <p>[3] Asp, M., Giacomello, S., Larsson, L., Wu, C., Fürth, D., Qian, X., ... & Lundeberg, J. (2019). A spatiotemporal organ-wide gene expression and cell atlas of the developing human heart. <em>Cell</em>, <em>179</em>(7), 1647-1660.</p>
FIGURE. Sanicula orthacantha in the wild (China, Chongqing, Nanchuan, Jinfo Shan, the type locality of S. nanchuanensis). A. Habitat. B. Habit. C. Leaves (left: adaxial surface; right: abaxial surface). D. Portion of inflorescence (side view). E. Portion of inflorescence (top view). F. Involucrate bracts. G. Umbellule (side view), a) involucellate bracteoles, b) calyx teeth. H. Staminate flowers (side view). I. Fertile flower with fruit. J. Mericarps. in Taxonomic studies on the genus Sanicula (Apiaceae) from China ( ): The clarification of some morphological distinction between S. orthacantha var. orthacantha and S. orthacantha var. brevispina, with the reduction of S. petagnioides to the synonymy of the former, and S. orthacantha var. stolonifera to
FIGURE. Sanicula orthacantha in the wild (China, Chongqing, Nanchuan, Jinfo Shan, the type locality of S. nanchuanensis). A. Habitat. B. Habit. C. Leaves (left: adaxial surface; right: abaxial surface). D. Portion of inflorescence (side view). E. Portion of inflorescence (top view). F. Involucrate bracts. G. Umbellule (side view), a) involucellate bracteoles, b) calyx teeth. H. Staminate flowers (side view). I. Fertile flower with fruit. J. Mericarps.
FIGURE. Sanicula orthacantha in the wild (China, Jiangxi, Jiujiang, Lushan, the type locality of S. orthacantha). A. Habitat. B. Habit. C. Leaves (left: adaxial surface; right: abaxial surface). D. Portion of inflorescence (side view). E. Portion of inflorescence (top view). F. Involucrate bracts. G. Umbellule (side view), a) involucellate bracteoles, b) calyx teeth. H. Staminate flowers (side view). I. Fertile flower with fruit, style, petals and calyx teeth. J. Mericarps in Taxonomic studies on the genus Sanicula (Apiaceae) from China ( ): The clarification of some morphological distinction between S. orthacantha var. orthacantha and S. orthacantha var. brevispina, with the reduction of S. petagnioides to the synonymy of the former, and S. orthacantha var. stolonifera to
FIGURE. Sanicula orthacantha in the wild (China, Jiangxi, Jiujiang, Lushan, the type locality of S. orthacantha). A. Habitat. B. Habit. C. Leaves (left: adaxial surface; right: abaxial surface). D. Portion of inflorescence (side view). E. Portion of inflorescence (top view). F. Involucrate bracts. G. Umbellule (side view), a) involucellate bracteoles, b) calyx teeth. H. Staminate flowers (side view). I. Fertile flower with fruit, style, petals and calyx teeth. J. Mericarps
FIGURE. Sanicula orthacantha var. brevispina in the wild (China, Sichuan, Emei Shan, the type locality of S. orthacantha var. brevispina and S. orthacantha var. stolonifera). A. Habitat and habit. B. Rhizome. C. Leaves (left: adaxial surface; right: abaxial surface). D. Portion of inflorescence (side view). E. Portion of inflorescence (top view). F. Involucrate bracts. G. Umbellule (side view), a) involucellate bracteoles, b) calyx teeth. H. Staminate flowers (side view). I. Fertile flower with fruit, style, petals and calyx teeth. J. Mericarps. in Taxonomic studies on the genus Sanicula (Apiaceae) from China ( ): The clarification of some morphological distinction between S. orthacantha var. orthacantha and S. orthacantha var. brevispina, with the reduction of S. petagnioides to the synonymy of the former, and S. orthacantha var. stolonifera to
FIGURE. Sanicula orthacantha var. brevispina in the wild (China, Sichuan, Emei Shan, the type locality of S. orthacantha var. brevispina and S. orthacantha var. stolonifera). A. Habitat and habit. B. Rhizome. C. Leaves (left: adaxial surface; right: abaxial surface). D. Portion of inflorescence (side view). E. Portion of inflorescence (top view). F. Involucrate bracts. G. Umbellule (side view), a) involucellate bracteoles, b) calyx teeth. H. Staminate flowers (side view). I. Fertile flower with fruit, style, petals and calyx teeth. J. Mericarps.
Distribution. SC China, known only from the type locality in Wanglang Nature Reserve, Pingwu County, N Sichuan Province. Distributional limits are not known. in Gliridae
Distribution. SC China, known only from the type locality in Wanglang Nature Reserve, Pingwu County, N Sichuan Province. Distributional limits are not known.
FIGURE. Phylogenetic tree derived from Bayesian analysis, based on nrLSU data. Posterior probability (PP> 0.95) values from the Bayesian analysis are added at the nodes. The scale bar represents the number of nucleotide changes per site. (T) indicates the type specimen for this species. The new species are in bold. in Four new species of Entoloma (Entolomataceae, Agaricomycetes) subgenera Cyanula and Claudopus from Vietnam and their phylogenetic position
FIGURE. Phylogenetic tree derived from Bayesian analysis, based on nrLSU data. Posterior probability (PP> 0.95) values from the Bayesian analysis are added at the nodes. The scale bar represents the number of nucleotide changes per site. (T) indicates the type specimen for this species. The new species are in bold.
Subspecies and Distribution. P. l. longimembris Coues, 1875 — SW USA (Mojave Desert and Transverse Ranges, SW California). P. l. aestivus Huey, 1928 — NW Mexico (W base Sierra Juarez to Valle de la Trinidad, N Baja California). P.l. arizonensis Goldman, 1931 — SW USA (SC Utah and NC Arizona to SE Nevada). P. l.bangsi Mearns, 1898 — SW USA (W Colorado Desert of S California). P. l. bombycinus Osgood, 1907 — SW USA and NW Mexico (lower Colorado River Valley of SE California, SW Arizona, NE Baja California, and NW Sonora). P. l. brevinasus Osgood, 1900 — SW USA (arid coastal basins of SW California). P. l. gulosus Hall, 1941 — W USA (along the W margin of former Pleistocene Lake Bonneville in the Great Basin of E Nevada and W Utah). P. l. internationalis Huey, 1939 — SW USA and NW Mexico (SC California and adjacent NC Baja California). P. l. kinoensis Huey, 1935 — NW Mexico (disjunct and geographically restricted population along Bahia Kino, W Sonora), but may be extinct. P. l. nevadensis Merriam, 1894 — W USA (Great Basin of SE Oregon, NE California, and NC Nevada). P. l. pacificus Mearns, 1898 — SW USA (coastal plains of SW California to the USA-Mexico border). P. I. panamintinus Merriam, 1894 — SW USA (Great Basin of W Nevada and SE California). P. l. pimensis Huey, 1937 — SW USA (disjunct distribution in SC Arizona). P. l. salinensis Bole, 1937 — SW USA (restricted distribution in the Salinas Valley of SE California). P. l. tularensis Richardson, 1937 — SW USA (restricted distribution in the upper valley of the Kern River, SC California). P. l. venustus Huey, 1930 — NW Mexico (known only from the type locality of San Agustin, NC Baja California). in Heteromyidae
Subspecies and Distribution. P. l. longimembris Coues, 1875 — SW USA (Mojave Desert and Transverse Ranges, SW California). P. l. aestivus Huey, 1928 — NW Mexico (W base Sierra Juarez to Valle de la Trinidad, N Baja California). P.l. arizonensis Goldman, 1931 — SW USA (SC Utah and NC Arizona to SE Nevada). P. l.bangsi Mearns, 1898 — SW USA (W Colorado Desert of S California). P. l. bombycinus Osgood, 1907 — SW USA and NW Mexico (lower Colorado River Valley of SE California, SW Arizona, NE Baja California, and NW Sonora). P. l. brevinasus Osgood, 1900 — SW USA (arid coastal basins of SW California). P. l. gulosus Hall, 1941 — W USA (along the W margin of former Pleistocene Lake Bonneville in the Great Basin of E Nevada and W Utah). P. l. internationalis Huey, 1939 — SW USA and NW Mexico (SC California and adjacent NC Baja California). P. l. kinoensis Huey, 1935 — NW Mexico (disjunct and geographically restricted population along Bahia Kino, W Sonora), but may be extinct. P. l. nevadensis Merriam, 1894 — W USA (Great Basin of SE Oregon, NE California, and NC Nevada). P. l. pacificus Mearns, 1898 — SW USA (coastal plains of SW California to the USA-Mexico border). P. I. panamintinus Merriam, 1894 — SW USA (Great Basin of W Nevada and SE California). P. l. pimensis Huey, 1937 — SW USA (disjunct distribution in SC Arizona). P. l. salinensis Bole, 1937 — SW USA (restricted distribution in the Salinas Valley of SE California). P. l. tularensis Richardson, 1937 — SW USA (restricted distribution in the upper valley of the Kern River, SC California). P. l. venustus Huey, 1930 — NW Mexico (known only from the type locality of San Agustin, NC Baja California).
Distribution. NW Argentina, known only from the type locality in the Salar de Pipanaco, S Catamarca Province. in Octodontidae
Distribution. NW Argentina, known only from the type locality in the Salar de Pipanaco, S Catamarca Province.
Subspecies and Distribution. C.s.sclateriBroom,1907—fromBeaufortWestEalongKoueveldbergeandSneeubergetoGraaff-Reinet,WesternandEasternCapeprovinces,SSouthAfrica. C.s.guwillarmodiRoberts,1936—fromextremeEFreeStateandSWKwaZulu-NatalSthroughLesothotoCEasternCapeProvince,SouthAfrica. C.s.montanaRoberts,1924—knownonlyfromthetypelocalitynearWakkerstroom,MpumalangaProvince,ESouthAfrica. C. s. shortridgei Broom, 1950 — known only from the type locality in Sutherland, Northern Cape Province, W South Africa. in Chrysochloridae
Subspecies and Distribution. C.s.sclateriBroom,1907—fromBeaufortWestEalongKoueveldbergeandSneeubergetoGraaff-Reinet,WesternandEasternCapeprovinces,SSouthAfrica. C.s.guwillarmodiRoberts,1936—fromextremeEFreeStateandSWKwaZulu-NatalSthroughLesothotoCEasternCapeProvince,SouthAfrica. C.s.montanaRoberts,1924—knownonlyfromthetypelocalitynearWakkerstroom,MpumalangaProvince,ESouthAfrica. C. s. shortridgei Broom, 1950 — known only from the type locality in Sutherland, Northern Cape Province, W South Africa.
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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.