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Figure 9 in Systematics of the Miocene-Recent bryozoan genus Pentapora (Cheilostomata)
Figure 9. Pentapora lacryma sp. nov., scanning electron micrographs of uncoated specimens from the Pliocene Coralline Crag Formation of Suffolk, England, imaged using back-scattered electrons. A, ovicellate autozooids and giant avicularia partly obscured by diagenetic cement, Aldeburgh Member, Aldeburgh Hall, NHM BZ 5677. B, C, E, F, Aldeburgh Member, Crag Pit Nursery, Aldeburgh, NHM BZ 5648. B, autozooids from encrusting base. C, growing edge of encrusting base showing ovicellate zooids and a few giant avicularia. E, ovicellate zooids with closure plates and a giant avicularium (left). F, ovicell (pores obscured by diagenetic cement) and giant avicularium. D, holotype with ovicellate zooids showing evenly porous ooecia, Broom Hill, NHM D50716. Scale bars: A = 55 Mm; B = 240 Mm; C = 520 Mm; D = 230 Mm; E = 150 Mm; F = 130 Mm.
Figure 8 in Systematics of the Miocene-Recent bryozoan genus Pentapora (Cheilostomata)
Figure 8. Pentapora pertusa (Milne Edwards, 1836), scanning electron micrographs of uncoated specimens from the Pliocene Coralline Crag Formation of Suffolk, England, imaged using back-scattered electrons. A, autozooids and several giant avicularia, Broom Pit, NHM D50182. B, ovicellate zooids and giant suboral avicularium with details obscured by diagenetic cement, Aldeburgh Member, Aldeburgh Hall, NHM BZ 5643. C–F, NHM BZ 5676,?Ramsholt Member, Broom Pit. C, patch of colony dominated by ovicellate zooids. D, ovicells and normal suboral avicularia. E, orifice and normal suboral avicularium. F, giant triangular suboral avicularium. Scale bars: A = 280 Mm; B = 190 Mm; C = 520 Mm; D = 220 Mm; E = 60 Mm; F = 100 Mm.
Figure 10 in Systematics of the Miocene-Recent bryozoan genus Pentapora (Cheilostomata)
Figure 10.?Pentapora lacryma sp. nov., scanning electron micrographs of uncoated specimens from the Pliocene Red Crag Formation of Walton-on-Naze, Essex, England, imaged using back-scattered electrons. A, B, NHM D34979(a). A, autozooids and giant avicularia. B, broken ovicells and a giant avicularium (left). C, D, NHM D34979(b). C, autozooids with and without the outer aragonitic layer of the frontal shield. D, autozooid preserving the aragonite layer, sometimes merging across zooidal boundaries (arrow). Scale bars: A = 430 Mm; B = 210 Mm; C = 170 Mm; D = 160 Mm.
Figure 6 in Systematics of the Miocene-Recent bryozoan genus Pentapora (Cheilostomata)
Figure 6. Pentapora fascialis (Pallas, 1766), scanning electron micrographs of uncoated fossil specimens imaged using backscattered electrons. A–C, Lower Pleistocene, Arda stream, Castell'Arquato, Piacenza, Emilia, Italy, NHM BZ 5669. A, colony fragment showing zooids with normal and giant avicularia, and ovicells overgrown by secondary calcification. B, giant avicularium in autozooid having primary orifice almost obscured by lappets forming a bridge. C, ovicell. D–F, Pliocene, Emilian, Gillina, Calabria, Italy. D, E, NHM BZ 5664. D, autozooids, showing normal avicularia and a giant avicularium, and a broken ovicell. E, ovicell. F, NHM BZ 5667. bases of oral spines (arrows). Scale bars: A = 300 Mm; B = 150 Mm; C, E = 120 Mm; D = 200 Mm; F = 110 Mm.
Figure 7 in Systematics of the Miocene-Recent bryozoan genus Pentapora (Cheilostomata)
Figure 7. Pentapora ottomulleriana (Moll, 1803), Monterosso al Mare, Liguria, Italy, NHM 2007.9.14.16; scanning electron micrographs of uncoated specimens imaged using back-scattered electrons. A, autozooids. B, ovicell. C, young zooids at the growing edge. D, autozooids and an avicularium. E, primary orifice. F, avicularium. Scale bars: A = 600 Mm; B = 100 Mm; C = 350 Mm; D = 200 Mm; E = 75 Mm; F = 130 Mm.
Figure 5 in Systematics of the Miocene-Recent bryozoan genus Pentapora (Cheilostomata)
Figure 5. Pentapora fascialis (Pallas, 1766), scanning electron micrographs of uncoated recent specimens imaged using back-scattered electrons. A, B, Tino Island, Italy, NHM 2007.9.14.14. A, group of autozooids, some with ovicells. B, autozooidal orifice and giant suboral avicularium. C, D, Oran, Algeria, NHM 1963.9.4.8. C, edge of branch showing autozooids (most with normal suboral avicularia) and marginal kenozooids. D, orifice and normal suboral avicularium. E, F, reputedly from Port Western, South Australia, NHM 34.2.20.15. E, inferred predator boreholes (arrowed) in frontal shields. F, giant suboral avicularia. Scale bars: A = 280 Mm; B = 100 Mm; C = 470 Mm; D = 60 Mm; E = 300 Mm; F = 100 Mm.
Figure 4 in Systematics of the Miocene-Recent bryozoan genus Pentapora (Cheilostomata)
Figure 4. Pentapora fascialis (Pallas, 1766), Tino Island, Italy, NHM 2007.9.14.14; scanning electron micrographs of coated specimens imaged using secondary electrons. A, autozooids. B, growing edge. C, primary orifice. D, oblique profile of normal suboral avicularium. Scale bars: A = 0.5 mm; B = 0.4 mm; C = 100 Mm; D = 0.5 mm.
Figure 3 in Systematics of the Miocene-Recent bryozoan genus Pentapora (Cheilostomata)
Figure 3. Pentapora foliacea (Ellis & Solander, 1786); scanning electron micrographs of uncoated specimens imaged using back-scattered electrons. A–C, NHM 2009.1.28.2, Littlehampton, Sussex, England. A, young autozooids close to growing edge. B, older autozooids. C, primary orifice of a young autozooid. D, primary orifice, Boreray, St Kilda, Scotland, NHM 1985.1.10.54. E–F, Persier Reef, Plymouth, Devon, England, NHM 2007.9.14.2. E, young ovicell. F, older ovicell embedded in secondary calcification. Scale bars: A = 290 Mm; B = 180 Mm; C, D = 60 Mm; E, F = 100 Mm.
Figure 2 in Systematics of the Miocene-Recent bryozoan genus Pentapora (Cheilostomata)
Figure 2. Pentapora foliacea (Ellis & Solander, 1786), Skomer Nature Reserve, Watwick, Dyfed, Wales, NHM 2007.9.14.5; scanning electron micrographs of coated specimens imaged using secondary electrons. A, old autozooids. B, growing edge and a kenozooid (left of centre). C, primary orifice. D, ovicellate zooids. E, autozooids, many with small suboral avicularia. F, oblique profile of suboral avicularium. Scale bars: A, B = 0.4 mm; C = 150 Mm; D, E = 0.4 mm; F = 40 Mm.
Figure 1 in Systematics of the Miocene-Recent bryozoan genus Pentapora (Cheilostomata)
Figure 1. Large colonies of the cheilostome bryozoan Pentapora. A, eschariform colony of Pentapora foliacea (Ellis & Solander, 1786), British waters, NHM 2009.1.28.3. B, adeoniform colony of Pentapora fascialis (Pallas, 1766), NHM 2001.1.25.4, near Marseille. Scale bars: A = 4 cm; B = 2 cm.
FIGURE 2 in Descriptions of the males of two recently described South African Panurginae (Hymenoptera: Andrenidae), with updated keys to the African species of Melitturga and Meliturgula
FIGURE 2: a, Melitturga (Australomelitturga) penrithorum gonostyli; b, Melitturga (Australomelitturga) barbareae gonostyli. Scale = 0.33mm.
Data from: Using singleton densities to detect recent selection in Bos taurus
<p>Many quantitative traits are subject to polygenic selection, where several genomic regions undergo small, simultaneous changes in allele frequency that collectively alter a phenotype. The widespread availability of genome data, along with novel statistical techniques, has made it easier to detect these changes. We apply one such method, the 'Singleton Density Score', to the Holstein breed of<i> Bos taurus</i> to detect recent selection (arising up to around 740 years ago). We identify several genes as candidates for targets of recent selection, including some relating to cell regulation, catabolic processes, neural-cell adhesion and immunity. We do not find strong evidence that three traits that are important to humans – milk protein content, milk fat content, and stature – have been subject to directional selection. Simulations demonstrate that since <i>B. taurus</i> recently experienced a population bottleneck, singleton numbers are reduced limiting the power of SDS methods. These results inform on which genes underlie recent genetic change in <i>B. </i><i>taurus</i>, while providing information on how polygenic selection can be best investigated in future studies.</p>
FIGURE 28 in On the recent Cyclocypridinae (Podocopida, Candonidae) with description of two new genera and one new species 2820
FIGURE 28. Physocypria bullata Vávra, 1897. A—lectotype, ♀ (MNB 10011); B, C—♂ (ZMH 1242b): A—T1, B—T2; C— hemipenis; D—T1. Scales = 0.1 mm.
FIGURE 14 in On the recent Cyclocypridinae (Podocopida, Candonidae) with description of two new genera and one new species 2820
FIGURE 14. Keysercypria deformis (Klie, 1940). A-E, lectotype ♂ (ZMH 550a), F-H paralectotype ♀ (ZMH 550b): A—last three segments of T2; B—last two segments of A2; C—right prehensile palp; D—left prehensile palp; E—hemipenis; F—UR; G—LV; H—RV: I—carapace, dorsal view. Scales = 0.1 mm. G-I modified after Klie (1940) and not to scale.
FIGURE 15 in On the recent Cyclocypridinae (Podocopida, Candonidae) with description of two new genera and one new species 2820
FIGURE 15. Keysercypria longiseta (Klie, 1930). A-F, lectotype ♂ (ZMH 937a); G-I. paralectotype ♀ (ZMH 937b): A—last two segments of A2; B—last five segments of A1; C—hemipenis; D—T2; E—right prehensile palp; F—left prehensile palp; G—LV; H—RV, I—carapace, dorsal view. Scales = 0.1 mm. G-I modified after Klie (1930) and not to scale.
FIGURE 2 in The recently proposed odonatan 'suborder' Cephalozygoptera: fact or fiction
FIGURE 2. Heads of Sieblosiidae and Lestidae. A, Stenolestes falloti (Théobald, 1937), holotype MNHN-F-B.24507. B, Undescribed Lestidae (late Eocene, Tibet, China). Scale bars = 5 mm (A), 2 mm (B).
FIGURE 1 in The recently proposed odonatan 'suborder' Cephalozygoptera: fact or fiction
FIGURE 1. Lestes ceresti Nel & Papazian, 1985, holotype MNHN-F-R.07445, Head. A, Part. B, Counterpart. Scale bars = 5 mm.
FIGURE 1 in Comparison of the recently described early Permian paoliid genus Permomertovia with the 'eoblattid' genera of the families Permulidae and Permotermopsidae
FIGURE 1. Permula lebachensis (Schlechtendal, 1913), specimen PE2021/5003. A, Part. B, Counterpart, arrows: weak arculus. Scale bars = 10 mm.
Supplementary data for "Recent increase in global land evapotranspiration is overestimated"
<p>Supplementary data for "Recent increase in global land evapotranspiration is overestimated"</p>
FIGURE 6 in A recently discovered species of Apiomorpha Rübsaamen (Hemiptera: Coccoidea: Eriococcidae) with unusual gall morphology
FIGURE 6. Phylogeny of 11 species of Apiomorpha based on a maximum parsimony (MP) analysis of mtDNA sequence data (COII) using an equal-weights scheme. Numbers above branches are bootstrap support values from 100 pseudoreplicates (MP/ ML).
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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.