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550 results for “taxonomic implications”
Supporting Data for "Exploring ChatGPT-4 for Transforming Taxonomic Data into OWL: Lessons Learned and Implications for Ontology Development"
<p>Data from the trials with ChatGPT to generate OWL files for taxonomic data from the GBIF Backbone Taxonomy.</p> <p>Updates of version 2: additional prompts from the experiments with Gemini and DeepSeek.</p>
First genetic data for the Critically Endangered Cuban endemic Zapata Rail Cyanolimnas cerverai, and the taxonomic implications
<p>Data associated with the publication First genetic data for the Critically Endangered Cuban endemic Zapata Rail <em>Cyanolimnas cerverai</em>, and the taxonomic implications.</p>
Fig. 7 in Taxonomic revision of West African cone snails (Gastropoda: Conidae) based upon mitogenomic studies: implications for conservation
Fig. 7 (opposite page). Kalloconus canariensis sp. nov. A–B. Holotype (dorsal and ventral views), 89.0 mm (MNCN 15.05/200091H). C. Paratype 1, 85.3 mm (MNCN 15.05/200091P). D. Paratype 5, 76.3 mm (MNCN 15.05/200092). E. Paratype 3, 92.1 mm (MNCN 15.05/200093). F. Paratype 2, 132.0 mm (MNCN 15.05/200094). G. Paratype 4, 93.9 mm (MNCN 15.05/200092). H. Paratype 6, 47.4 mm (MNCN 5.05.200091P). I. Paratype 7, 43.3 mm (MNCN 15.05/200095). J–K. Radular tooth. K. K. canariensis sp. nov., paratype 1. K. K. pulcher ([Lightfoot], 1786), Joal Fadiouth, Senegal (MJT), SL = 96.7 mm. Scale bars = 10 mm unless otherwise indicated
Fig. 8 in Taxonomic revision of West African cone snails (Gastropoda: Conidae) based upon mitogenomic studies: implications for conservation
Fig. 8. Plot of maximum diameter (MD, mm) versus shell length (SL, mm) for K. canariensis sp. nov. (Ɨ) and K. pulcher ([Lightfoot], 1786) (-). The lectotype of K. siamensis (Hwass in Bruguiére, 1792) (A) is also shown.
Fig. 6 in Taxonomic revision of West African cone snails (Gastropoda: Conidae) based upon mitogenomic studies: implications for conservation
Fig. 6 (opposite page). A. Conus navarroi navarroi Rolán, 1986, holotype, 16 mm (MNCN 15.05/1008). B. Africonus angeluquei Tenorio, Abalde & Zardoya, 2018 (= perrineae Cossignani & Fiadeiro, 2018), holotype, 30.0 mm (MNCN 15.05/78710). C. Conus raulsilvai Rolán, Monteiro & Fernandes, 1998, holotype, 19.7 mm (MNCN 15.05/27230). D. Conus regonae Rolán & Trovão, 1990, holotype, 32.7 mm (MNCN 15.05/1092). E. Conus roeckeli Rolán, 1980, holotype, 13.2 mm (MNCN 15.05/1049). F. Africonus salletae Cossignani, 2014, holotype, 15.5 mm (MMM). G. Africonus santaluziensis Cossignani & Fiadeiro, 2015, paratype, 28.1 mm (Paul Kersten coll.). H. Africonus santanaensis Afonso & Tenorio, 2014, holotype, 17.1 mm (MNCN 15.05/60118). I. Conus saragasae Rolán, 1986, holotype, 21.8 mm (MNCN 15.05/1009). J. Africonus verdensis (Trovão, 1979), 22.5 mm (MNCN 15.05/78864). K. Conus vulcanus Tenorio & Afonso, 2004, holotype, 25.2 mm (MNCN 15.05/46652). L. Chelyconus ermineus (Born, 1778), 54.3 mm (MNCN 15.05/80014). M. Genuanoconus genuanus (Linnaeus, 1758), 50.2 mm (MNCN 15.05/78547). N. Kalloconus ateralbus (Kiener, 1850), 40.1 mm (MNCN 15.05/79649). O. Kalloconus byssinus (Röding, 1798), 56.4 mm (MNCN 15.05/90429). Scale bars = 10 mm.
Fig. 2 in Taxonomic revision of West African cone snails (Gastropoda: Conidae) based upon mitogenomic studies: implications for conservation
Fig. 2. Phylogenetic relationships of West African cones and species delimitation. A time tree (relaxed molecular clock) was reconstructed following methods and calibrations in Abalde et al. (2017a). Dates are in million years. Bold names indicate new mitogenomes. A red line indicates the threshold (uncorrected p distance of 0.2%, based on the divergences between Africonus verdensis (Trovão, 1979) and its sister group and Varioconus guanche (Lauer, 1993) and its sister group) for species delimitation.
Fig. 10 in Taxonomic revision of West African cone snails (Gastropoda: Conidae) based upon mitogenomic studies: implications for conservation
Fig. 10 (opposite page). A. Conus ambiguus Reeve, 1844, neotype, 39.3 mm (NBC). B. Conus bellocqae van Rossum, 1996, paratype, 60 mm (F. Gubbioli coll., Marbella, Spain). C. Monteiroconus tabidus (Reeve, 1844), 33.6 mm (MNCN 15.05/78864). D. Conus belairensis Pin & Leung Tack in Pin, 1989, holotype, 36.7 mm (MNHN IM-2000-32668). E. Varioconus bruguieresi (Kiener, 1846) comb. nov., 32.1 mm (MNCN 15.05/78497). F. Varioconus cloveri (Walls, 1978) comb. nov., 23.2 mm (MNCN 15.05/78457). G. Varioconus echinophilus (Petuch, 1975b) comb. nov., 22.0. mm (MNCN 15.05/90430). H. Conus franciscanus Hwass in Bruguière, 1792, lectotype, 56.6 mm (MHNG-MOLL-52625). I. Varioconus franciscanus (Hwass in Bruguière, 1792) comb. nov., 53.6 mm (MNCN 15.05/78491). J. Varioconus franciscanus f. hybridus (Kiener, 1847), 40.0 mm (MNCN 15.05/78427). K. Conus guanche Lauer, 1993, holotype, 34.0 mm (MNHN IM-2000-2553). L. Conus guinaicus Hwass in Bruguière, 1792, lectotype, 43.0 mm (MHNG-MOLL-52638). M. Varioconus guinaicus (Hwass in Bruguière, 1792) comb. nov., 50.2 mm (MNCN 15.05/78443). N. Lautoconus wolof Petuch & Berschauer, 2018, holotype, 21.1 mm (MNHN IM-2000-34015). O. Conus pineaui Pin & Leung Tack in Pin, 1989, holotype, 28.7 mm (MNHN IM-2000-2528). P. Conus dorotheae Monnier & Limpalaër, 2010, holotype, 26.8 mm (MNHN IM-2009-8702). Scale bars = 10 mm.
Fig. 4 in Taxonomic revision of West African cone snails (Gastropoda: Conidae) based upon mitogenomic studies: implications for conservation
Fig. 4 (opposite page). A. Conus felitae Rolán, 1990, holotype, 12.7 mm (MNCN 15.05/1099). B. Africonus fernandesi (Tenorio, Afonso & Rolán, 2008), 14.5 mm (MNCN 15.05/78598). C. Africonus freitasi Tenorio, Afonso, Rolán, Pires, Vasconcelos, Abalde & Zardoya, 2018, holotype, 13.7 mm (MNCN 15.05/200008) D. Conus verdensis furnae Rolán, 1990, holotype, 21.1 mm (MNCN 15.05/1097). E. Africonus fuscoflavus (Röckel, Rolán & Monteiro, 1980), 22.3 mm (MNCN 15.05/80407). F. Conus damottai galeao Rolán, 1990, holotype, 21.3 mm (MNCN 15.05/1093). G. Africonus gonsaloi Afonso & Tenorio, 2014, holotype, 19.3 mm (MNCN 15.05/60119). H. Africonus grahami (Röckel, Cosel & Burnay, 1980), 24.0 mm (MNCN 15.05/78549). I. Conus infinitus Rolán, 1990, holotype, 20.8 mm (MNCN, 15.05/1095). J. Conus isabelarum Tenorio & Afonso, 2004, holotype, 22.8 mm (MNCN 15.05/46654). K. Conus josephinae Rolán, 1980, holotype, 25.8 mm (MNCN 15.05/1050). L. Africonus kersteni (Tenorio, Afonso & Rolán, 2008), holotype, 20.8 mm (MNCN 15.05/47051). M. Africonus longilineus (Röckel, Rolán & Monteiro, 1980), 21.7 mm (MNCN 15.05/79738). N. Africonus lugubris (Reeve, 1849), 14.5 mm (MNCN 15.05/90431). O. Africonus maioensis (Trovão, Rolán & Félix-Alves, 1990), 29.5 mm (MNCN 15.05/78689). P. Africonus miruchae (Röckel, Rolán & Monteiro, 1980), 12.9 mm (MNCN 15.05/79789). Scale bars = 10 mm.
Fig. 1. A in A new Mississippian hexactinellid sponge from the western Gondwana: Taxonomic and paleobiogeographic implications
Fig. 1. A. Geographic location of the studied area. B. Geological map and location of the studied section. The west flank of the Agua Quemada Syncline is divided in some tectonic blocks (1 and 2) by inverse and dextral strip faults. Sponges come from nodules of equivalent fine-grained dark stratigraphical intervals of the Agua de Lucho Formation (Tournaisian), cropping out under glacigenic diamictitic in both tectonic blocks. C. Stratigraphic column of the Agua de Lucho Formation and the location of the sponge-bearing levels.
Fig. 2 in A new Mississippian hexactinellid sponge from the western Gondwana: Taxonomic and paleobiogeographic implications
Fig. 2. Hexactinellid sponge Minitaspongia parvis gen. et sp. nov. from the Tournaisian Carboniferous, Sierra de las Minitas section, La Rioja Province, Argentina. A. Holotype PULR-I 4, complete obconical specimen, showing the cylindrical acute base. External surface of the holotype showing deep impressions of vertical and horizontal tracts and cross-shaped spicule molds as second order elements in the middle of first order quadrules (A2). B. Paratype PULR-I 5, external impression with original spicules forming the reticulate skeleton (B1); detail showing a well preserved external area of the second order quadrules (B2); detail of the first order quadrules showing preserved hexactine-based spicules aligned (B3); detail of the tract with vertically oriented, main long axis hexactine- based spicules, bundles of two or three long spicule axis occur in the tract (B4); enlarged section of B4 showing nodes of the perpendicular axis of the hexactins (B5); details of the spicules in the tracts, long rayed hexactins, and small second order hexactins with equal-ray dimensions (B6, B7).
Fig. 3. A in A new Mississippian hexactinellid sponge from the western Gondwana: Taxonomic and paleobiogeographic implications
Fig. 3. A. Schematic reconstruction of the complete sponge Minitaspongia parvis gen et. sp. nov. B. The spicule framework of the wall as main parts of the vertical and horizontal bands.
Figure 6 in The record of Torosaurus (Ornithischia: Ceratopsidae) in Canada and its taxonomic implications
Figure 6. Osteohistology of Torosaurus cf. T. latus (EM P16.1). A, thin section of cortical bone of left femoral diaphysis ('B9- 3') (red bounding boxes indicate details in B); B, details of A, showing poorly vascularized periosteum (left) and deep cortex (right). Arrow indicates possible line of arrested growth. Note the lack of a discernible 'External Fundamental System' in B. Further imagery available at links in Appendix 2.
Figure 3 in The record of Torosaurus (Ornithischia: Ceratopsidae) in Canada and its taxonomic implications
Figure 3. Squamosals attributable to Torosaurus. A, EM P16.1; B, MPM VP6841; C, YPM 1830, holotype of T. latus (mirrored left squamosal). Note that EM P16.1 and MPM VP6841 share a wide squamosal blade, broadly rounded caudolateral corner (indicated by arrows) and a large fenestra within the blade. Squamosals scaled to same length to emphasize shape differences. Image in B provided by R. Hunt-Foster and image in C provided by A. Farke (used with permission).
Figure 2 in The record of Torosaurus (Ornithischia: Ceratopsidae) in Canada and its taxonomic implications
Figure 2. Parietosquamosal frill of Torosaurus cf. T. latus (EM P16.1.). A, dorsal surface; B, interpretive reconstruction of dorsal surface; C, schematic transverse cross-section of squamosal near caudal edge, based on sketch by H. Jones; D, schematic of frill, showing paired fossae and channels on ventral surface of squamosals, based on sketch by H. Jones. Abbreviations: p, parietal; pf, parietal fenestra; sq, squamosal; sqaf, accessory fenestra of squamosal; sqb, squamosal bar.
Figure 1 in The record of Torosaurus (Ornithischia: Ceratopsidae) in Canada and its taxonomic implications
Figure 1. Locality information pertinent to Canadian Torosaurus specimens. A, map (created using https://www. simplemappr.net/) showing locations of EM P16.1 and UALVP 1646 (stars). B, stratigraphic context of EM P16.1 and UALVP 1646, with distribution of Hell Creek Formation Torosaurus for context. Note that the precise placement of EM P16.1 within the Frenchman Formation is unknown. The precise location of MPM VP6841 within the upper Hell Creek Formation is likewise uncertain. Abbreviations: Fm, Formation; K-Pg, Cretaceous-Palaeogene boundary; Mtn, Mountain.
Figure 7 in The record of Torosaurus (Ornithischia: Ceratopsidae) in Canada and its taxonomic implications
Figure 7. Parietal of Torosaurus cf. T. latus (UALVP 1646). A, dorsal surface; B, interpretive reconstruction of dorsal surface; C, ventral surface; D, interpretive reconstruction ventral surface; E, detail of left parietal fenestra. Arrows in B and D indicate epiparietal loci. Arrows in E indicate unbroken margin of parietal fenestra. Abbreviations: mb, median bump; pf, parietal fenestra; pfo, parietal fossa.
Figure 5 in The record of Torosaurus (Ornithischia: Ceratopsidae) in Canada and its taxonomic implications
Figure 5. Osteohistology of Torosaurus cf. T. latus (EM P16.1). A, thin section of trabecular bone of left femoral metaphysis ('B9-2A') (red bounding box indicates detail in B); B, detail of A, showing large, subcircular erosion bays and dense, Haversian tissue; C, thin section of cortical bone of left femoral metaphysis ('B9-2B'), sampled immediately adjacent and superficial to A (red bounding box indicates detail in D); D, detail of C, showing periosteum. Arrows indicate lines of arrested growth. Note the lack of a discernible 'External Fundamental System' in D. Further imagery available at links in Appendix 2.
Fig. 9. N-dimensional morphospace for the 28 in Taxonomic implications of describing a new species of Loimia (Annelida, Terebellidae) with two size-dependent morphotypes
Fig. 9. N-dimensional morphospace for the 28 species of Loimia Malmgren, 1866, calculated for the larger (body length>100 mm, grey) and smaller (body length <100 mm, pink) species separately; red dots = larger and smaller individuals of Loimia davidi sp. nov.; large points with white borders = centroids of each hypervolume; hypervolume shape and boundaries defined by 5000 random points; table = summary of hypervolume richness, dispersion and evenness.
Fig. 10 in Taxonomic implications of describing a new species of Loimia (Annelida, Terebellidae) with two size-dependent morphotypes
Fig. 10. Original drawing of Terebella gigantea Montagu, 1819 by Eliza Dorville, included in Montagu (1819: pl. xi) and downloaded at http://biodiversitylibrary.org/page/758907 [accessed 12 Dec. 2018].
Fig. 5 in Taxonomic implications of describing a new species of Loimia (Annelida, Terebellidae) with two size-dependent morphotypes
Fig. 5. Loimia davidi sp. nov.A–C, G–H. Paratype CEAB A.P. 935B.D–F. Paratype MNCN 16.01/19140. A. Anterior fragment in ventral view. B. Anterior end in ventral view. C. Anterior end in lateral view. D. Anterior end in dorsal view. E. Anterior end in frontal view. F. Anterior end in lateral view, showing ocular spots. G. Posterior end in dorsal view. H. Detail of the pygidial papillae. Abbreviations: ll = lower lip; ll1 = first pair of lateral lappets; ll2 = second pair of lateral lappets; tm = tentacular membrane; ul =
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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.