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3,137 results for “morphological revision”
Fig. 1. Morphological characters used for the phylogenetic analysis and key. A–C. Terminal maxillary palpomere. D–E. Eyes. F–H. Pronotum. I–J. Leg. K–L in Taxonomic revision of the Lycocerus hanatanii species group (Coleoptera, Cantharidae), with the description of new species from Taiwan
Fig. 1. Morphological characters used for the phylogenetic analysis and key. A–C. Terminal maxillary palpomere. D–E. Eyes. F–H. Pronotum. I–J. Leg. K–L. Inner margin of dorsal plate of aedeagus.
Fig. 8 in A revision of the Thyropygus allevatus group. Part V: Nine new species of the extended opinatus subgroup, based on morphological and DNA sequence data (Diplopoda: Spirostreptida: Harpagophoridae)
Fig. 8. Thyropygus sutchariti sp. nov., from Kaeng Krachan, holotype (CUMZ-D00090), ♂, gonopods. A. Anterior view, left telopodite removed. B. Posterior view, left telopodite removed. C. Left telopodite, posterior-mesal view. D. Left telopodite, anterior-lateral view.
Fig. 11. A in A revision of the Thyropygus allevatus group. Part V: Nine new species of the extended opinatus subgroup, based on morphological and DNA sequence data (Diplopoda: Spirostreptida: Harpagophoridae)
Fig. 11. A. Thyropygus navychula sp. nov., specimen from Surin Islands, living ♂ (paratype, CUMZ-D00089-1). B. Thyropygus forceps sp. nov., specimen from Namwang Srithammasokrach, living ♂ (paratype, CUMZ-D00073-1).
Fig. 5 in A revision of the Thyropygus allevatus group. Part V: Nine new species of the extended opinatus subgroup, based on morphological and DNA sequence data (Diplopoda: Spirostreptida: Harpagophoridae)
Fig. 5. Thyropygus mesocristatus sp. nov., from Srikasorn, holotype (CUMZ-D00094), ♂, gonopods. A. Anterior view, left telopodite removed. B. Posterior view, left telopodite removed. C. Lateral view. D. Left telopodite, posterior-mesal view. E. Left telopodite, anterior-lateral view.
Fig. 2 in A revision of the Thyropygus allevatus group. Part V: Nine new species of the extended opinatus subgroup, based on morphological and DNA sequence data (Diplopoda: Spirostreptida: Harpagophoridae)
Fig. 2. Thyropygus cimi sp. nov., from Namwang Srithammasokrach, holotype (CUMZ-D00086), ♂, gonopods. A. Anterior view, left telopodite removed. B. Posterior view, left telopodite removed. C. Lateral view. D. Left telopodite, posterior-mesal view. E. Left telopodite, anterior-lateral view.
Fig. 1 in A revision of the Thyropygus allevatus group. Part V: Nine new species of the extended opinatus subgroup, based on morphological and DNA sequence data (Diplopoda: Spirostreptida: Harpagophoridae)
Fig. 1. Phylogenetic relationships of Thyropygus species based on maximum likelihood analysis (ML) and Bayesian Inference (BI) of 1147 bp of concatenated gene fragments of COI (660 bp) and 16S rRNA (487 bp). Numbers at nodes indicate branch support based on bootstrapping (ML) / posterior probability (BI). Scale bar = 0.06 substitutions/site. # indicates branches which received <50% ML bootstrap support, - indicates non-supported branches by posterior probability. Clade memberships and designations are shown as vertical bars; 1A1 = T. allevatus, 1A2 = cuisinieri subgroup, 1A3 = opinatus subgroup and 1A4 = induratus subgroup. The coloured area marks the T. opinatus subgroup. Abbreviations after species names refer to locality names as shown in Table 1.
Fig. 7 in A revision of the Thyropygus allevatus group. Part V: Nine new species of the extended opinatus subgroup, based on morphological and DNA sequence data (Diplopoda: Spirostreptida: Harpagophoridae)
Fig. 7. Thyropygus planispina sp. nov., from Tham Sua temple, holotype (CUMZ-D00088), ♂, gonopods. A. Anterior view, left telopodite removed. B. Posterior view, left telopodite removed. C. Lateral view. D. Left telopodite, posterior-mesal view. E. Left telopodite, anterior-lateral view.
Fig. 6 in A revision of the Thyropygus allevatus group. Part V: Nine new species of the extended opinatus subgroup, based on morphological and DNA sequence data (Diplopoda: Spirostreptida: Harpagophoridae)
Fig. 6. Thyropygus navychula sp. nov., from Surin Islands, holotype (CUMZ-D00095), ♂, gonopods. A. Anterior view, left telopodite removed. B. Posterior view, left telopodite removed. C. Left telopodite, posterior-mesal view. D. Left telopodite, anterior-lateral view.
Fig. 4 in A revision of the Thyropygus allevatus group. Part V: Nine new species of the extended opinatus subgroup, based on morphological and DNA sequence data (Diplopoda: Spirostreptida: Harpagophoridae)
Fig. 4. Thyropygus forceps sp. nov., gonopods. – A, C–E. Holotype (CUMZ-D00092), ♂, from Namwang Srithammasokrach. A. Anterior view, left telopodite removed. C. Posterior view, left telopodite removed. D. Left telopodite, posterior-mesal view. E. Left telopodite, anterior-lateral view. – B. Specimen from Tham Pha Deang temple (CUMZ-D00093), ♂. Anterior view, left telopodite removed.
Fig. 10 in A revision of the Thyropygus allevatus group. Part V: Nine new species of the extended opinatus subgroup, based on morphological and DNA sequence data (Diplopoda: Spirostreptida: Harpagophoridae)
Fig. 10. Thyropygus ursus sp. nov., from Lanta Islands, holotype (NMHW-Inv.7855), ♂, gonopods. A. Anterior view, left telopodite removed. B. Posterior view, left telopodite removed. C. Left telopodite, posterior-mesal view. D. Left telopodite, anterior-lateral view.
Fig. 9 in A revision of the Thyropygus allevatus group. Part V: Nine new species of the extended opinatus subgroup, based on morphological and DNA sequence data (Diplopoda: Spirostreptida: Harpagophoridae)
Fig. 9. Thyropygus undulatus sp. nov., from Khao Phanom Bencha, holotype (CUMZ-D00087), ♂, gonopods. A. Anterior view, left telopodite removed. B. Posterior view, left telopodite removed. C. Lateral view. D. Left telopodite, posterior-mesal view. E. Left telopodite, anterior-lateral view.
Fig. 3 in A revision of the Thyropygus allevatus group. Part V: Nine new species of the extended opinatus subgroup, based on morphological and DNA sequence data (Diplopoda: Spirostreptida: Harpagophoridae)
Fig. 3. Thyropygus culter sp. nov., from Rorn waterfall, holotype (CUMZ-D00091), ♂, gonopods. A. Anterior view, left telopodite removed. B. Posterior view, left telopodite removed. C. Left telopodite, posterior-mesal view. D. Left telopodite, anterior-lateral view.
Fig. 4 in Taxonomic revision of Australian Amobia Robineau-Desvoidy, 1830 (Sarcophagidae: Miltogramminae): integrating morphology and genetics finds a new species and tackles old problems
Fig. 4. Amobia burnsi (Malloch, 1930), ♂, NSW, North Head, Sydney Harbour, 14 Feb. 1978, G. Daniels leg. (AM) A. Habitus, lateral view. B. Head, lateral view. C. Habitus, dorsal view. D. Head, dorsal view. E. Abdomen, dorsal view. F. Left wing, dorsal view. G. Head, anterior view. Scale bars: 1 mm.
Fig. 1 in Taxonomic revision of Australian Amobia Robineau-Desvoidy, 1830 (Sarcophagidae: Miltogramminae): integrating morphology and genetics finds a new species and tackles old problems
Fig. 1. Maximum likelihood phylogenetic tree indicating the placement of Amobia among the global Miltogramminae, inferred from COI, CYTB, ND4 and EF1α sequence data. With the exception of the three newly sequenced Australian Amobia and Macronychia rubesca, data was acquired from Piwczyński et al. (2017). Node support values are shown for both maximum likelihood analysis (bootstrap support, 1000 iterations; in bold font) and Bayesian analysis (posterior probability, 40 million generations), 'NA' indicates nodes resolved that were not resolved by the Bayesian analysis. Branch length scale = 0.3 nucleotide substitutions per site (calculated by the GTR+G nucleotide substitution model).
Fig. 6 in Taxonomic revision of Australian Amobia Robineau-Desvoidy, 1830 (Sarcophagidae: Miltogramminae): integrating morphology and genetics finds a new species and tackles old problems
Fig. 6. Amobia serpenta sp. nov., holotype, ♂, NT, Serpentine Gorge, West MacDonnell National Park, 13 Nov. 2017, Johnston, Wallman and Szpila leg. (ANIC). A. Habitus, lateral view. B. Head, lateral view. C. Habitus, dorsal view. D. Head, dorsal view. E. Abdomen, dorsal view. F. Left wing, dorsal view. G. Head, anterior view. Scale bars: 1 mm.
Fig. 3 in Taxonomic revision of Australian Amobia Robineau-Desvoidy, 1830 (Sarcophagidae: Miltogramminae): integrating morphology and genetics finds a new species and tackles old problems
Fig. 3. Amobia auriceps (Baranov, 1935), male terminalia, QLD, Cairns, 1919, J.F. Illingworth leg. (BM). A. Epandrium, cerci, surstyli and phallus, posterior view. B. Epandrium, cerci, surstyli, phallus and pre-gonite, lateral view. Abbreviations: c = cercus; d = distal lobe of phallus; s = surstylus; p = pregonite. Scale bars: 100 µm.
Fig. 5 in Taxonomic revision of Australian Amobia Robineau-Desvoidy, 1830 (Sarcophagidae: Miltogramminae): integrating morphology and genetics finds a new species and tackles old problems
Fig. 5. Amobia burnsi (Malloch, 1930), male terminalia, NT, 15 km N Katherine, 16 May 2005, R.W. Matthews leg (ANIC). A. Epandrium, cerci, surstyli and phallus, posterior view. B. Epandrium, cerci, surstyli, phallus and pre-gonite, lateral view. C. SEM image of epandrium, gonites, cerci and surstyli, posterior view. D. SEM image of epandrium, gonites, phallus, cerci and surstyli, lateral view. Abbreviations: c = cercus; d = distal lobe of phallus; s = surstylus; p = pre-gonite. Scale bars: 100 µm.
Fig. 25 in Revision of the morphology, phylogenetic relationships, behaviour and diversity of the Iberian and Italian ant-like Tachydromia Meigen, 1803 (Diptera: Hybotidae)
Fig. 25. Habitat of Tachydromia ebejeri Gonçalves, Grootaert & Andrade sp. nov. in a forest of Quercus pyrenaica Willd. in Portugal, Arganil, Benfeita (Mata da Margaraça), a region under submediterranean influence.
Fig. 24 in Revision of the morphology, phylogenetic relationships, behaviour and diversity of the Iberian and Italian ant-like Tachydromia Meigen, 1803 (Diptera: Hybotidae)
Fig. 24. Forest of Fagus sylvatica L. in the Apennine Mountains, where Tachydromia apterygon Plant & Deeming, 2006 can be found.
Fig. 21 in Revision of the morphology, phylogenetic relationships, behaviour and diversity of the Iberian and Italian ant-like Tachydromia Meigen, 1803 (Diptera: Hybotidae)
Fig. 21. Drawings of the tip of stenopterous wings and images obtained by scanning electron microscope (SEM) of the micropterous wings. Males are pictured in the left column, females in the right. A, C. T. pandellei (Séguy, 1941). B–C. T. pieltaini (Gil Collado, 1936). D–E. T. semiaptera (Gil Collado, 1923). F–G. T. stenoptera Gonçalves, Grootaert & Andrade sp. nov. Scale bars: A–D, F = 50 µm; E, G = 10 µm.
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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.