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FIGURE 4 in Morphological studies and molecular data on a new marine ciliate, Apokeronopsis sinica n. sp. (Ciliophora: Urostylida), from the South China Sea
FIGURE 4. Unmatched sites from SSrRNA gene sequences alignment. Numbers represent the positions of the nucleotides. Missing sites are compensated by gaps (-). Matched sites are marked with dots (.).
FIGURE 3 in Morphological studies and molecular data on a new marine ciliate, Apokeronopsis sinica n. sp. (Ciliophora: Urostylida), from the South China Sea
FIGURE 3. Comparison of Apokeronopsis species. A. crassa (A, B, from Song et al. 2004), A. wrighti (C, D, from Long et al. 2008), A. antarctica (E, F, from Petz 1995), A. ovalis (G, H, from Shao et al. 2009), A. bergeri (I, J, from Li et al. 2008), and A. sinica (K, L, original), to show the morphology of live cells (A, C, E, G, I, K), infraciliature (B, D, F, H, J, L). Scale bars in (A, B, I, J) =100 µm, in (C–H, K, L) = 60 µm.
FIGURE 2 in Morphological studies and molecular data on a new marine ciliate, Apokeronopsis sinica n. sp. (Ciliophora: Urostylida), from the South China Sea
FIGURE 2. Photomicrographs of Apokeronopsis sinica n. sp. from live cells (A–E, I, J) and after protargol impregnation (K–O), and ventral views of live cells of A. crassa (F), A. bergeri (G) and A. wrighti (H). (A) Ventral view of the typical specimen. (B) Ventral view, showing the contractile vacuole (arrow). (C) Lateral view. (D) Ventral view of the anterior portion, arrows indicate the cilia of adoral zone of membranelles, arrowheads mark the paroral membranes and double-arrowheads depict the buccal cirri. (E) Lateral view to show the large cortical granules distributed on dorsal side. (I) Ventral view, to show the cortical granules: vermeil large (arrows), colorless large (arrowheads) and colorless small ones (double-arrowheads). (J) Ventral view, showing the cortical granules between the cirri rows. (K) infraciliature of the ventral side of a typical specimen. (L) Ventral view of the anterior portion, arrow indicates the paroral membrane and arrowhead marks the endoral membrane. (M) Ventral view of the anterior-right portion, arrowheads refer to frontoterminal cirri, and arrows show the buccal cirri. (N) Macronuclear nodules. (O) Ventral view of the posterior portion, note the transverse cirri (arrows). Scale bars in (A, B, C, F, G, H) = 100 µm, in (K) = 80 µm.
FIGURE 1. Apokeronopsis sinica n in Morphological studies and molecular data on a new marine ciliate, Apokeronopsis sinica n. sp. (Ciliophora: Urostylida), from the South China Sea
FIGURE 1. Apokeronopsis sinica n. sp. from live cells (A–D) and after protargol impregnation (E–F). (A, B) Ventral views of two typical specimens. (C) Dorsal view; to show the sparsely distributed large granules. (D) Details of the cortex, double-arrowheads indicate the smaller cortical granules, arrows mark the vermeil larger ones and arrowheads mark the colorless larger ones. (E, F) Ventral and dorsal views of the infraciliature and nuclear apparatus. AZM = adoral zone of membranelles; BC = buccal cirri; BiC = bicoronal cirri; DK = dorsal kineties; EM = endoral membrane; FTC = frontoterminal cirri; LMR = left marginal row; Ma = macronuclei; MC = midventral complex; PM = paroral membrane; RMR = right marginal row; TC = transverse cirri. Scale bars = 80 µm.
Data from: Molecular dynamics simulation of the interaction between palmitic acid and high pressure CO2
<p>In this study, molecular dynamics simulation was used to explore the interaction characteristics of palmitic acid and CO2, and the effects of temperature and pressure on the solubility of palmitic acid in CO2 were investigated. In the range of 293K-353K and 5MPa-30MPa, the snapshot of palmitic acid distribution in CO2 shows that the molecular chain of palmitic acid in high-density CO2 system is more straight and more dispersed than that in low-density CO2 system. The radial distribution function further clearly shows that the solubility of palmitic acid in CO2 decreases with the increase of temperature and increases with the increase of pressure, which is consistent with the fatty acid solubility data reported in the literature and the setting rules of supercritical CO2 extraction process conditions. As the temperature decreases and the pressure increases, the interaction energy between palmitic acid and CO2 increases, which is conducive to overcoming the intermolecular force of palmitic acid and promoting dissolution. The solubility parameters of palmitic acid and CO2 can better reflect the trend of palmitic acid solubility changing with temperature and pressure, which can play a guiding role in the determination of process conditions and even the development of new processes.</p>
Figure 9 in Species delimitation in the Andean grasshopper genus Orotettix Ronderos & Carbonell (Orthoptera: Melanoplinae): an integrative approach combining morphological, molecular and biogeographical data
Figure 9 Orotettix males. Phallic complex, species as indicated. A, D, G, J, M, distal portion of aedeagal valves, lateral view; B, E, H, K, N, distal portion of aedeagal valves, dorsal view; C, F, I, L, O, epiphallus, dorsal view. Numbers indicate characters and states used in the phylogenetic analyses.
Figure 11 in Species delimitation in the Andean grasshopper genus Orotettix Ronderos & Carbonell (Orthoptera: Melanoplinae): an integrative approach combining morphological, molecular and biogeographical data
Figure 11 Outgroup taxa used in the phylogenetic analyses, species as indicated. A–D, male habitus. Scale bars: 5 mm. Numbers indicate characters and states used in the phylogenetic analyses.
Figure 12 in Species delimitation in the Andean grasshopper genus Orotettix Ronderos & Carbonell (Orthoptera: Melanoplinae): an integrative approach combining morphological, molecular and biogeographical data
Figure 12 Outgroup taxa used in the phylogenetic analyses, species as indicated. A, C, E, G, male distal abdominal segments, dorsal view; B, D, F, H, male distal abdominal segments, lateral view. Numbers indicate characters and states used in the phylogenetic analyses.
Figure 7 in Species delimitation in the Andean grasshopper genus Orotettix Ronderos & Carbonell (Orthoptera: Melanoplinae): an integrative approach combining morphological, molecular and biogeographical data
Figure 7 Orotettix males, species as indicated. A, C, E, G, I, distal abdominal segments, lateral view; B, D, F, H, J, distal abdominal segments, dorsal view. Numbers indicate characters and states used in the phylogenetic analyses.
Figure 4 in Species delimitation in the Andean grasshopper genus Orotettix Ronderos & Carbonell (Orthoptera: Melanoplinae): an integrative approach combining morphological, molecular and biogeographical data
Figure 4 Combined molecular and morphological phylogenetic analysis under parsimony criteria, using an extended implied weighting strategy. Numbers indicate branch supports (symmetric resampling).
Figure 5 in Species delimitation in the Andean grasshopper genus Orotettix Ronderos & Carbonell (Orthoptera: Melanoplinae): an integrative approach combining morphological, molecular and biogeographical data
Figure 5 Orotettix, phallic complex, in lateral (A) and dorsal views (B). Abbreviations: Ap, apodemes of cingulum; Ar, arch of aedeagus; Av, aedeagal valves; Ep, endophallic plates; E, epiphallus; L, lophi of epiphallus; Rm, rami; Sh, sheath of aedeagus.
Figure 13 in Species delimitation in the Andean grasshopper genus Orotettix Ronderos & Carbonell (Orthoptera: Melanoplinae): an integrative approach combining morphological, molecular and biogeographical data
Figure 13 Outgroup taxa used in the phylogenetic analyses, species as indicated. Phallic complex. A, D, G, J, distal portion of aedeagal valves, lateral view; B, E, H, K, distal portion of aedeagal valves, dorsal view; C, F, I, L, epiphallus, dorsal view. Numbers indicate characters and states used in the phylogenetic analyses.
Figure 3 A in Species delimitation in the Andean grasshopper genus Orotettix Ronderos & Carbonell (Orthoptera: Melanoplinae): an integrative approach combining morphological, molecular and biogeographical data
Figure 3 A, most parsimonious tree of the genus Orotettix (length 55, CI = 0.87, RI = 0.97) resulting from the cladistic analysis of the morphological character dataset, under equal weights. Black circles indicate unique changes and white circles indicate homoplasies. The numbers below the nodes are bootstrap support values, and those above are Bremer support values. The new species (O. sp. 1; O. sp. 2; O. sp. 3; O. sp. 4; O. sp. 5) delimited in this study based on molecular, morphological and geographical analyses are indicated in the tree. Lateral bars indicate the distribution of the specimens according to the geomorphic units of the Andes delimited by Gonzalez & Pfiffner (2012). B, geomorphological units of the Andes delimited by Gonzalez & Pfiffner (2012).
Figure 8 in Species delimitation in the Andean grasshopper genus Orotettix Ronderos & Carbonell (Orthoptera: Melanoplinae): an integrative approach combining morphological, molecular and biogeographical data
Figure 8 Orotettix males, species as indicated. A, C, E, G, I, distal abdominal segments, lateral view; B, D, F, H, J, distal abdominal segments, dorsal view. Numbers indicate characters and states used in the phylogenetic analyses.
Figure 10 in Species delimitation in the Andean grasshopper genus Orotettix Ronderos & Carbonell (Orthoptera: Melanoplinae): an integrative approach combining morphological, molecular and biogeographical data
Figure 10 Orotettix males. Phallic complex, species as indicated. A, D, G, J, M, distal portion of aedeagal valves, lateral view; B, E, H, K, N, distal portion of aedeagal valves, dorsal view; C, F, I, L, O, epiphallus, dorsal view. Numbers indicate characters and states used in the phylogenetic analyses.
Figure 2 in Species delimitation in the Andean grasshopper genus Orotettix Ronderos & Carbonell (Orthoptera: Melanoplinae): an integrative approach combining morphological, molecular and biogeographical data
Figure 2 Bayesian phylogenetic analysis of COI characters. Acronyms of specimens according to Table 1. Numbers on branches indicate posterior probabilities. Numbers in parentheses indicate bootstrap supports of maximum-parsimony analysis. Results of General Mixed Yule-coalescent (GMYC) analysis are represented as lateral bars with different line patterns. Each bar indicates a different cluster identified by GMYC. Solid black patterns indicate clusters which coincide with species delimitation based on results from the other molecular, morphological and geographical analyses. 1, O. andeanus; 2, O. sp. 1; 3, O. sp. 2; 4, O. hortensis; 5, O. sp. 3; 6, O. sp. 4; 7, O. carrascoi; 8, O. sp. 5; 9, O. ceballosi.
Figure 6 in Species delimitation in the Andean grasshopper genus Orotettix Ronderos & Carbonell (Orthoptera: Melanoplinae): an integrative approach combining morphological, molecular and biogeographical data
Figure 6 Orotettix males, species as indicated. A–J, habitus. Scale bars: 5 mm. Numbers indicate characters and states used in the phylogenetic analyses.
Figure 1 in Species delimitation in the Andean grasshopper genus Orotettix Ronderos & Carbonell (Orthoptera: Melanoplinae): an integrative approach combining morphological, molecular and biogeographical data
Figure 1 Geographical distribution of Orotettix species (except for O. laevis), considering all specimens examined in this study. The map was produced with QGIS 2.4 Chugiak.
Figure 9. A–D in A new genus of African Acrometopini (Tettigoniidae: Phaneropterinae) based on morphology, chromosomes, acoustics, distribution, and molecular data, and the description of a new species
Figure 9. A–D, left cercus of male Altihoratosphaga species. A, Altihoratosphaga hanangensis sp. nov. B, Altihoratosphaga nou. C, Altihoratosphaga montivaga. D, Altihoratosphaga nomima. All specimens were collected from Ruaha National Park. Scale bar: 2 mm. E–H, subgenital plates of male Altihoratosphaga species. E, A. hanangensis sp. nov. F, A. nou. G, A. montivaga. H, A. nomima. All specimens were collected from Ruaha National Park. Scale bar: 2 mm. I, right tegmen of male A. hanangensis sp. nov. Scale bar: 0.5 cm. J, subgenital plate of female A. hanangensis sp. nov. Scale bar: 1 mm. K, ovipositor of A. hanangensis sp. nov. Scale bar: 1 mm.
Figure 8. A–D in A new genus of African Acrometopini (Tettigoniidae: Phaneropterinae) based on morphology, chromosomes, acoustics, distribution, and molecular data, and the description of a new species
Figure 8. A–D, lateral view of the pronotum and dorsal view of the abdominal apex of male Altihoratosphaga species. A, Altihoratosphaga hanangensis sp. nov., paratype. B, Altihoratosphaga nou, paratype. C, Altihoratosphaga montivaga. D, Altihoratosphaga nomima, holotype. E–H, dorsal view of abdominal apex of male Altihoratosphaga species. E, A. hanangensis sp. nov., paratype. F, A. nou, paratype. G, A. montivaga. H, A. nomima, holotype I, dorsal aspect of male pronotum of A. hanangensis sp. nov. Note the triangle-shaped posterior part of the pronotum. J, lateral view of abdominal apex of female A. hanangensis sp. nov., paratype. K, reduced alae of female A. montivaga. Scale bars: 2 mm.
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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.