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5,436 results for “phylogenetic species”
Fig 13. Carrhotus taprobanicus Simon, 1902. A–B. Male habitus. A. Dorsal view. B. Ventral view. C–D. Female habitus. C. Dorsal view. D. Ventral view. E–F. Palp. E. Ventral view. F. Retrolateral view. G in Phylogenetic placement of Carrhotus Thorell, 1891 with three new species from Sri Lanka (Araneae: Salticidae)
Fig 13. Carrhotus taprobanicus Simon, 1902. A–B. Male habitus. A. Dorsal view. B. Ventral view. C–D. Female habitus. C. Dorsal view. D. Ventral view. E–F. Palp. E. Ventral view. F. Retrolateral view. G. Epigynum, ventral view. Abbreviations: E = embolus; PEB = posterior epigynal border; PLP = posterior lateral protrusion; RTA = retrolateral tibial apophysis; TE = tegulum. Scale bars: A–D = 2 mm; E–F = 0.2 mm; G = 0.1 mm.
Fig 12. Carrhotus silanthi Caleb, 2020.A–B. Palp.A. Ventral view.B. Retrolateral view.C–D. Epigynum. C. Ventral view. D in Phylogenetic placement of Carrhotus Thorell, 1891 with three new species from Sri Lanka (Araneae: Salticidae)
Fig 12. Carrhotus silanthi Caleb, 2020.A–B. Palp.A. Ventral view.B. Retrolateral view.C–D. Epigynum. C. Ventral view. D. Dorsal view. Abbreviations: AG = accessory gland; E = embolus; FD = fertilization duct; RTA = retrolateral tibial apophysis; S = spermatheca; TE = tegulum. Scale bars: A–B = 0.2 mm; C–D = 0.1 mm.
Fig 9 in Phylogenetic placement of Carrhotus Thorell, 1891 with three new species from Sri Lanka (Araneae: Salticidae)
Fig 9. Carrhotus lobatus sp. nov., palp. A. Ventral view. B. Retrolateral view. Abbreviations: E = embolus; PLP = posterior lateral protrusion; RTA = retrolateral tibial apophysis; TE = tegulum. Scale bars = 0.2 mm.
Fig 7 in Phylogenetic placement of Carrhotus Thorell, 1891 with three new species from Sri Lanka (Araneae: Salticidae)
Fig 7. Carrhotus atratus sp. nov. A–B. Palp. A. Ventral view. B. Retrolateral view. C. Epigynum ventral view. D. Vulva dorsal view. Abbreviations: AG = accessory gland; CO = copulatory opening; E = embolus; FD = fertilization duct; PLP = posterior lateral protrusion; RTA = retrolateral tibial apophysis; S = spermatheca; TE = tegulum. Scale bars: A–B = 0.2 mm; C–D = 0.1 mm.
Fig. 11. Carrhotus silanthi Caleb, 2020. A–B. Male habitus. A. Dorsal view. B. Ventral view. C–D. Female habitus. C. Dorsal view. D. Ventral view. E–H. Palp. E–F in Phylogenetic placement of Carrhotus Thorell, 1891 with three new species from Sri Lanka (Araneae: Salticidae)
Fig. 11. Carrhotus silanthi Caleb, 2020. A–B. Male habitus. A. Dorsal view. B. Ventral view. C–D. Female habitus. C. Dorsal view. D. Ventral view. E–H. Palp. E–F. Ventral view; the arrows showing the embolus tip directed in clockwise (11E) or directed in apical (11F). G–H. Retrolateral view. Abbreviations: PLP = posterior lateral protrusion; RTA = retrolateral tibial apophysis; TE = tegulum. Scale bars: A–D = 2 mm; E–H = 0.2 mm.
Three new species of Macrostomum (Platyhelminthes, Macrostomorpha), with notes on taxonomy and phylogenetics
<p>The deposited folders contain image material of free-living flatworm specimens. These data support the following publication: Shi Y, Zeng Z, Wang J, Zhang S, Deng L, Wang A (2022) Three new species of <em>Macrostomum</em> (Platyhelminthes, Macrostomorpha) from China and Australia, with notes on taxonomy and phylogenetics. ZooKeys 1099: 1-28. <a href="https://doi.org/10.3897/zookeys.1099.72964">https://doi.org/10.3897/zookeys.1099.72964</a></p> <p>For more information about these specimens see also https://macrostomorpha.myspecies.info</p>
Fig 8 in Phylogenetic placement of Carrhotus Thorell, 1891 with three new species from Sri Lanka (Araneae: Salticidae)
Fig 8. Carrhotus lobatus sp. nov. A–B. Male habitus. A. Dorsal view. B. Ventral view. C–D. Palp, C. Ventral view. D. Retrolateral view. Abbreviations: E = embolus; PLP = posterior lateral protrusion; RTA = retrolateral tibial apophysis; TE = tegulum. Scale bars: A–B = 2 mm; C–D = 0.2 mm.
Fig 4 in Phylogenetic placement of Carrhotus Thorell, 1891 with three new species from Sri Lanka (Araneae: Salticidae)
Fig 4. Carrhotus albosetosus sp. nov. A. Epigynum, ventral view. B. Vulva, dorsal view. Abbreviations: AG = accessory gland; CO = copulatory opening; FD = fertilization duct; S = spermatheca. Scale bars = 0.1 mm.
Fig 1 in Phylogenetic placement of Carrhotus Thorell, 1891 with three new species from Sri Lanka (Araneae: Salticidae)
Fig 1. The single most likely tree obtained by ML analysis of the combined molecular data in RAxML– VI–HPC. The numbers above the nodes represent bootstrap values (only values 50 and above are given). Nodes that are unsupported have been collapsed. Collection country is given if available. In life images: A. Carrhotus albosetosus sp. nov. from Pillikutuwa. B. C. taprobanicus Simon, 1902 from Gomaraya. C. C. silanthi Caleb, 2020 from Ussangoda. D. C. silanthi from Giants Tank Sanctuary. E. C. atratus sp. nov. from Hiyare. F. C. viduus from Mandaitivu.
Fig 3 in Phylogenetic placement of Carrhotus Thorell, 1891 with three new species from Sri Lanka (Araneae: Salticidae)
Fig 3. Carrhotus albosetosus sp. nov., female. A. Habitus, dorsal view. B. Habitus, ventral view. C. Epigynum. Scale bars: A–B = 2 mm; C = 0.1 mm.
Fig 6 in Phylogenetic placement of Carrhotus Thorell, 1891 with three new species from Sri Lanka (Araneae: Salticidae)
Fig 6. Carrhotus atratus sp. nov. A–B. Male habitus. A. Dorsal view. B. Ventral view. C–D. Female habitus. C. Dorsal view. D. Ventral view. E–F. Palp. E. Ventral view. F. Retrolateral view. G. Epigynum. Abbreviations: E = embolus; PLP = posterior lateral protrusion; RTA = retrolateral tibial apophysis. Scale bars: A–D = 2 mm; E–F = 0.2 mm; G = 0.1 mm.
Fig 10 in Phylogenetic placement of Carrhotus Thorell, 1891 with three new species from Sri Lanka (Araneae: Salticidae)
Fig 10. Photographs of live Carrhotus silanthi Caleb, 2020, males. A–C. From Giants Tank Sanctuary. D–F. From Ussangoda.
Fig. 32. Slaterocoris breviatus, male genitalia. A in Revision And Phylogenetic Analysis Of The North American Genus Slaterocoris Wagner With New Synonymy, The Description Of Five New Species And A New Genus From Mexico, And A Review Of The Genus Scalponotatus Kelton (Heteroptera: Miridae: Orthotylinae)
Fig. 32. Slaterocoris breviatus, male genitalia. A. Progress, BC. B, K. Cedar Creek Recreation Area, ID. C, O. Peshtigo River, WI. D–F, I. Washington, DC. J. Pine Grove Furnace State Park, PA. L. Slave Lake, AB. M. Ingonish, NS. N. Chiwaukee Prairie, WI.
Fig. 33. Slaterocoris pallidicornis, male genitalia. A, D, F–I in Revision And Phylogenetic Analysis Of The North American Genus Slaterocoris Wagner With New Synonymy, The Description Of Five New Species And A New Genus From Mexico, And A Review Of The Genus Scalponotatus Kelton (Heteroptera: Miridae: Orthotylinae)
Fig. 33. Slaterocoris pallidicornis, male genitalia. A, D, F–I. Theodore Roosevelt National Park, ND. B, C, E, J, K. Beddeck, NS. L. Pingree Park, CO.
The impact of species phylogenetic relatedness on invasion varies distinctly along resource versus nonresource environmental gradients
<p><span>Understanding why certain plant communities are vulnerable to alien invasive species is essential to predicting and controlling invasion in a changing environment. Darwin's naturalization hypothesis suggests that non-native species should be more successful in communities where their close relatives are absent. Empirical tests of this hypothesis, however, have produced mixed results. Using plot-level data from natural forests along elevational transects covering strong environmental gradients, we examined whether the invasion of the globally invasive species <em>Ageratina adenophora</em> can be explained by environmental filtering and/or competition from closely related species linked to environmental gradients. Abundant precipitation, warm temperatures, open canopies, and postfire environments facilitated <em>A. adenophora</em> invasion, whereas resident taxonomic richness suppressed its invasion. Importantly, we found that invader-resident relatedness had a strong negative effect on invader cover under resource scarcity conditions (e.g., low water availability), but not under nonresource environmental stress conditions (e.g., low temperature). Our findings help reconcile the varied applicability of Darwin's naturalization hypothesis to biological invasions in a changing world.</span></p>
Fig. 4 in A new species of the genus Cottus (Scorpaeniformes, Cottidae) from the Baltic Sea Basin and its phylogenetic placement
Fig. 4. The result of statistical analysis of morphometric characters of type and non-type specimens of Cottus cyclophthalmus sp. nov. from rivers Krasnaya, Neris, Šerkšnė, Siesartis, and Žeimena (method of principal components was used). The numbers correspond to the places where the sculpins were caught, as indicated on the map (Fig. 1).
Fig. 2 in A new species of the genus Cottus (Scorpaeniformes, Cottidae) from the Baltic Sea Basin and its phylogenetic placement
Fig. 2. Cottus cyclophthalmus sp. nov., holotype, ♂ (ZIN 56687), SL 83.3 mm, TL 99.0 mm, Krasnaya River, near Tokarevka village, 54º24'59.4" N 22º23'50.4" E. 3D scan images. a. Lateral view. b. Dorsal view. c. Ventral view.
Fig. 1 in A new species of the genus Cottus (Scorpaeniformes, Cottidae) from the Baltic Sea Basin and its phylogenetic placement
Fig. 1. The map of sampling sites showing the distribution of Cottus cyclophtalmus sp. nov. The numbers indicate sampling sites in various rivers: 1. Krasnaya River. 2. Neris River. 3. Žeimena River. 4. Siesartis River. 5. Šerkšnė River. The star marks the type locality of the new species; the circles mark sampling sites of non-type specimens; the triangle marks the locality where specimen of Cottus microstomus sp. nov. was caught.
Fig. 3 in A new species of the genus Cottus (Scorpaeniformes, Cottidae) from the Baltic Sea Basin and its phylogenetic placement
Fig. 3. The zoological picture of the holotype of Cottus cyclophthalmus sp. nov. (ZIN 56687), SL 83.3 mm, lateral view.
Fig. 5 in A new species of the genus Cottus (Scorpaeniformes, Cottidae) from the Baltic Sea Basin and its phylogenetic placement
Fig. 5. The result of the DFA carried out on morphometric characters to discriminateCottus cyclophthalmus sp. nov. (green), Cottus gobio Linnaeus, 1758 (blue), and Cottus koshewnikowi Gratzianov, 1907 (red).
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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.