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952 results for “revised taxonomy”
FIGURE 33 in Haasea Verhoeff, 1895-a genus of tumultuous history and chaotic recordsredefinition, revision of taxonomy and geographic distributions, with descriptions of two new species from Austria and Serbia (Diplopoda, Chordeumatida, Haaseidae)
FIGURE 33. Haasea makarovi sp. nov., paratype male (NHMW9473). A. Left anterior gonopod, mesal view. B. Right anterior gonopod, lateral view. C. Posterior gonopods, posterior view. Abbreviations: ab—anterior branch; alp—anterior lateral process; mb—medial branch; mdl—mesodistal lobe; mp—mesal process; pb—posterior branch; pl—posterior lamella; plp—posterior lateral process; s—sternum; t—telopodite. Scale bars: 0.1 mm.
FIGURE 34 in Haasea Verhoeff, 1895-a genus of tumultuous history and chaotic recordsredefinition, revision of taxonomy and geographic distributions, with descriptions of two new species from Austria and Serbia (Diplopoda, Chordeumatida, Haaseidae)
FIGURE 34. Haasea makarovi sp. nov., paratype male (NHMW9474). A. Right tarsus 3, anterior view. B. Leg 7, detail with ventral papillae, ventral view. C. Anterior gonopods, anterior view. D. Anterior gonopods, posterodistal view. E. Anterior gonopods, detail of distal part, anterior view. F. Anterior gonopods, detail of distal part, posterodistal view. Abbreviations: a—angiocoxite; alp—anterior lateral process; asl—anterior sternal lobe; f—furrow; mdl—mesodistal lobe; ml—"Opuntia- like" membranous; mp—mesal process; msp—medial sternal process; pc—papillated cone; plp—posterior lateral process; s—sternum; so—seminal opening; Scale bars: 0.1 mm (C, D), 0.05 mm (A, E, F), 0.01 mm (B).
FIGURE 37 in Haasea Verhoeff, 1895-a genus of tumultuous history and chaotic recordsredefinition, revision of taxonomy and geographic distributions, with descriptions of two new species from Austria and Serbia (Diplopoda, Chordeumatida, Haaseidae)
FIGURE 37. Haasea makarovi sp. nov., paratype female (IZB). A. Vulvae, ventral view. B. Postgenital plate, posterior view. C. Leg-pair 3, Anterior view. Abbreviations: b—bursa; o—operculum; sl—sternal lobe. Scale bars: 0.1 mm.
FIGURE 28 in Haasea Verhoeff, 1895-a genus of tumultuous history and chaotic recordsredefinition, revision of taxonomy and geographic distributions, with descriptions of two new species from Austria and Serbia (Diplopoda, Chordeumatida, Haaseidae)
FIGURE 28. Haasea gruberi sp. nov., holotype male (NHMW9470). A. Leg-pair 2, posterior view. B. Leg-pair 3, anterior view. C. Right leg 4, posterior view. D. Right leg 5, posterior view. E. Left leg 6, anterior view. F. Leg-pair 7, anterior view. G. Left leg 10, posterior view. H. Left leg 11, posterior view. Scale bars: 0.1 mm.
FIGURE 35 in Haasea Verhoeff, 1895-a genus of tumultuous history and chaotic recordsredefinition, revision of taxonomy and geographic distributions, with descriptions of two new species from Austria and Serbia (Diplopoda, Chordeumatida, Haaseidae)
FIGURE 35. Haasea makarovi sp. nov., A. Paratype male (IZB), left anterior gonopod, lateral view. B. Paratype male (IZB), left anterior gonopod, mesal view. C. Paratype male (IZB), left anterior gonopod, detail of distal part, lateral view. D. Paratype male (IZB), left anterior gonopod, detail of distal part, mesal view. E. Paratype male (NHMW9474), anterior gonopods, detail, posterodital view. F. Paratype male (NHMW9474), left posterior gonopod, mesal view. G. Paratype female (IZB), vulvae, ventral view. Abbreviations: a—angiocoxite; ab—anterior branch; alp—anterior lateral process; b—bursa; cp—coxal process; f—furrow; mb—medial branch; mdl—mesodistal lobe; ml—"Opuntia-like" membranous lobe; mp—mesal process; o—operculum; pb—posterior branch; pc—papillated cone; pgp—postgenital plate; plp—posterior lateral process; so—seminal opening; t—telopodite. Scale bars: 0.1 mm (A, B, F, G), 0.05 mm (C, D, E).
FIGURE 17 in Haasea Verhoeff, 1895-a genus of tumultuous history and chaotic recordsredefinition, revision of taxonomy and geographic distributions, with descriptions of two new species from Austria and Serbia (Diplopoda, Chordeumatida, Haaseidae)
FIGURE 17. Haasea inflata (Verhoeff, 1907), males from Posruck, Schlossberg, Austria. A. Habitus, lateral view. B. Left anterior gonopod, lateral view. C. Left anterior gonopod, mesal view. Scale bars: 1 mm (A), 0.1 mm (B, C).
FIGURE 14 in Haasea Verhoeff, 1895-a genus of tumultuous history and chaotic recordsredefinition, revision of taxonomy and geographic distributions, with descriptions of two new species from Austria and Serbia (Diplopoda, Chordeumatida, Haaseidae)
FIGURE 14. Haasea germanica (Verhoeff, 1901), male from Krummnussbaum, Austria. A–E. Left anterior gonopod. F–H. Right posterior gonopod. A. Mesal view. B. Lateral view. C. Distolateral view. D. Detail of distal part, mesal view. E. Detail of distal part, distal view. F, G. Posterior view. H. Mesal view. Abbreviations: a—angiocoxite; ab—anterior branch; asl—anterior sternal lobe; cp—coxal process; dp—distal part; f—furrow; mb—medial branch; mdl—mesodistal lobe; ml—"Opuntia-like" membranous lobe; mp—mesal process; pb—posterior branch; pc—papillated cone; pl—posterior lamella; plp—posterior lateral process; s—sternum; so—seminal opening; t—telopodite. Scale bars: 0.1 mm (A–C, F–H), 0.05 mm (D, E).
FIGURE 13 in Haasea Verhoeff, 1895-a genus of tumultuous history and chaotic recordsredefinition, revision of taxonomy and geographic distributions, with descriptions of two new species from Austria and Serbia (Diplopoda, Chordeumatida, Haaseidae)
FIGURE 13. Haasea germanica (Verhoeff, 1901), male from Krummnussbaum, Austria. A. Habitus, lateral view. B. Left anterior gonopod, lateral view. C. Left anterior gonopod, mesal view. Scale bars: 1 mm (A), 0.1 mm (B, C).
FIGURE 1. Living Haasea Verhoeff, 1895. A. H in Haasea Verhoeff, 1895-a genus of tumultuous history and chaotic recordsredefinition, revision of taxonomy and geographic distributions, with descriptions of two new species from Austria and Serbia (Diplopoda, Chordeumatida, Haaseidae)
FIGURE 1. Living Haasea Verhoeff, 1895. A. H. germanica (Verhoeff, 1901), female from Reiflding, Germany. B. H. ger- manica (Verhoeff, 1901), mating pair from Riedl, Germany. C. H. flavescens (Latzel, 1884), male from Schwaighofen, Austria. D. H. flavescens (Latzel, 1884), mating pair from Gaisberg, Austria. E. H. hungarica (Verhoeff, 1928), male from Fruška gora Mt., Serbia. F. H. vidinensis (Strasser, 1973a), female from the Ponor Radovanske reke Cave, Serbia. Photos credit: A–D. Jörg Spelda, E. Dragiša Savić (photo in lab), F. Nikola Vesović (photo in lab).
FIGURE 16 in Haasea Verhoeff, 1895-a genus of tumultuous history and chaotic recordsredefinition, revision of taxonomy and geographic distributions, with descriptions of two new species from Austria and Serbia (Diplopoda, Chordeumatida, Haaseidae)
FIGURE 16. Haasea hungarica (Verhoeff, 1928), male from Fruška gora Mt., Serbia. A. Right anterior gonopod, mesal view. B. Right anterior gonopod, lateral view. C. Right anterior gonopod, detail of distal part, mesal view. D. Left posterior gonopod, mesal view. E. Right posterior gonopod, mesal view. F. Right posterior gonopod, posterior view. Abbreviations: a—angiocoxite; ab—anterior branch; asl—anterior sternal lobe; cp—coxal process; dp—distal part; mb—medial branch; mdl—mesodistal lobe; ml—"Opuntia-like" membranous lobe; mp—mesal process; pb—posterior branch; pc—papillated cone; pl—posterior lamella; plp—posterior lateral process; so—seminal opening; t—telopodite. Scale bars: 0.1 mm (A, B, D–F), 0.05 mm (C).
Data from: Integrative taxonomy and species delimitation in harvestmen: a revision of the western North American genus Sclerobunus (Opiliones: Laniatores: Travunioidea)
Alpha taxonomy, and specifically the delimitation of species, is becoming increasingly objective and integrative. The use of coalescent-based methods applied to genetic data is providing new tools for the discovery and delimitation of species. Here, we use an integrative approach via a combination of discovery-based multivariate morphological analyses to detect potential new species. These potential species are then used as a priori species in hypothesis-driven validation analyses with genetic data. This research focuses on the harvestmen genus Sclerobunus found throughout the mountainous regions of western North America. Based on our analyses, we conduct a revision of Sclerobunus resulting in synonymy of Cyptobunus with Sclerobunus including transfer of S. cavicolens comb. nov. and elevation of both subspecies of S. ungulatus: S. ungulatus comb. nov. and S. madhousensis comb. nov., stat. nov. The three subspecies of S. robustus are elevated, S. robustus, S. glorietus stat. nov., and S. idahoensis stat. nov. Additionally, five new species of Sclerobunus are described from New Mexico and Colorado, including S. jemez sp. nov., S. klomax sp. nov., S. skywalkeri sp. nov., S. speoventus sp. nov., and S. steinmanni sp. nov. Several of the newly described species are single-cave endemics, and our findings suggest that further exploration of western North American cave habitats will likely yield additional new species.
Data from: The western spring beauties, Claytonia lanceolata (Montiaceae): a review and revised taxonomy for California
The taxonomic history of Claytonia lanceolata is fraught with confusion. Poor preservation of diagnostic characteristics on museum specimens and incomplete original descriptionsmade from limited reference material have resulted in inadequate characterization of morphological features and geographic distributions, particularly for plants in more xeric areas of California. In this paper, we investigate populations previously thought to belong to C. lanceolata and provide an updated taxonomy for Californian taxa based largely on morphological observations and geographic records. These data are corroborated by evidence of genetic polymorphisms and ecological divergence. Claytonia obovata was synonymized with C. lanceolata in 1966 and remained unrecognized until now because previous treatments misinterpreted morphological variation in C. lanceolata s. s. Claytonia peirsonii is a new combination for a species comprising four subspecies endemic to the Desert Southwest, three of which are new to science. Two new species are described here: Claytonia panamintensis, known in California only from the Panamint Mountains but ranging morewidely across southern Nevada, and Claytonia serpenticola. The latter species shares a similar geographic rangewith C. obovata in the Klamath-Siskiyou region of northern California and southwestern Oregon, and these two occur in close sympatry through much of their respective distributions. We also provide molecular evidence to support retention of the name C. lanceolata for populations in California that do not fall into any of the aforementioned new species or combinations. Taxa accepted in this paper are best distinguished from each other by their habitat (many are apparently edaphic endemics), betalain pigmentation, inflorescence architecture, and morphology of cauline leaves, subterranean stems, and flowers.
FIGURES 8-9. Fig. 8 in Hadena ligata Möschler (Lepidoptera: Noctuidae): distribution and revised taxonomy
FIGURES 8-9. Fig. 8. Larva of Dypterygia rozmani. 14 July 1989, reared ex ovo (coded: tlm 89-37) on Rumex crispus, Pine Bush, Albany County, New York. Fig. 9. Larva of Trachea delicata. 10 August 1989, reared ex ovo (coded: tlm 89-34) on Rumex crispus, Badlands, Slope County, North Dakota.
FIGURES 1-6. Fig. 1 in Hadena ligata Möschler (Lepidoptera: Noctuidae): distribution and revised taxonomy
FIGURES 1-6. Fig. 1. Dypterygia ligata, female habitus (expanse 37.0 mm). 7 May 1978, Fuch's Hammock nr. Homestead, Dade Co., Florida, T. Dickel. Fig. 2. Dypterygia ligata, female genitalia (length 5.0 mm) (gen. diss. McCabe 3466). Same data as Fig. 1. Fig. 3. Dypterygia ligata, male genitalia (expanse 4.0 mm) – valves (gen. diss. McCabe 3279). 15 January 1999, Key Largo Botanical Preserve, Munroe Co., Florida, T. McCabe. Fig. 4. Dypterygia ligata, male genitalia – same data as Fig. 3. Fig. 5. Dypterygia ordinarius, male genitalia – valves (gen. diss. McCabe 3543). 20 July 1986, Mt. St. Benedict, St. George's Co., Trinidad, H. Romack. Fig. 6. Dypterygia ordinarius, male genitalia – vesica – same data as Fig. 5.
FIGURE 2 in A new species of Ansonia Stoliczka 1872 (Anura: Bufonidae) from Central Peninsular Malaysia and a revised taxonomy for Ansonia from the Malay Peninsula
FIGURE 2. Upper: Female paratypes (ZRC 1.11561–62, 1.11564–65, left to right) of Ansonia latirostra. Holotype (ZRC 1.11559) on far left. Lower: Male paratypes (ZRC 1.11560, 1.11563, 1.11566, left to right) of A. latirostra. White bar = 15 mm.
FIGURE 1 in A new species of Ansonia Stoliczka 1872 (Anura: Bufonidae) from Central Peninsular Malaysia and a revised taxonomy for Ansonia from the Malay Peninsula
FIGURE 1. Distribution of Ansonia on the Malay Peninsula and adjacent islands. State borders are delimited for West Malaysia only.
FIGURE 21 in Revision of the pentacrinid stalked crinoids of the genus Endoxocrinus (Echinodermata, Crinoidea), with a study of environmental control of characters and its consequences for taxonomy
FIGURE 21. Relative growth rate of the four Bahamian phenotypes of Endoxocrinus and Neocrinus decorus revealed by Sr content of columnals (from David 1998). White spots: proximal columnals; black spots: distal columnals.
FIGURE 24 in Revision of the pentacrinid stalked crinoids of the genus Endoxocrinus (Echinodermata, Crinoidea), with a study of environmental control of characters and its consequences for taxonomy
FIGURE 24. Allopatric and sympatric differentiation of Atlantic and Pacific phenotypes in the genus Endoxocrinus.
FIGURE 23 in Revision of the pentacrinid stalked crinoids of the genus Endoxocrinus (Echinodermata, Crinoidea), with a study of environmental control of characters and its consequences for taxonomy
FIGURE 23. Estimation of the morphological disparity between Atlantic and Pacific phenotypes of diplocrinine crinoids (from David 1998). Semiquantitative estimate accumulates distinctive characters (main traits in external morphology and facet characters of articulations).
FIGURE 22 in Revision of the pentacrinid stalked crinoids of the genus Endoxocrinus (Echinodermata, Crinoidea), with a study of environmental control of characters and its consequences for taxonomy
FIGURE 22. Decrease in size related to depth in Atlantic and Pacific diplocrinine crinoids. For the northeastern Atlantic (dotted line), the number of specimens is obtained by multiplying by 20 (from Roux 1976). For the Caribbean (100500 m), stalk diameters between 2.1 to 3.5 mm correspond to more frequent juvenile specimens.
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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)
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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.