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FIGURE 19 in Bioacoustics and systematics of Mecopoda (and related forms) from South East Asia and adjacent areas (Orthoptera, Tettigonioidea, Mecopodinae) including some chromosome data
FIGURE 19. Tegmina in Mecopoda and Eumecopoda species. A M. angusta, male, B M. angusta, female, C M. divergens, female, holotype, photo without scale, size according to the description, D E. platyphoea stat. nov., female, holotype, E E. cyrtoscelis zhantievi subsp. nov., male, holotype, F E. cyrtoscelis zhantievi subsp. nov., female, paratype. Scale 10 mm.
FIGURE 9 in Bioacoustics and systematics of Mecopoda (and related forms) from South East Asia and adjacent areas (Orthoptera, Tettigonioidea, Mecopodinae) including some chromosome data
FIGURE 9. Oscillograms of the calling songs of species of the Mecopoda confracta subgroup. Details (1 s sections). In M. sismondoi sp. nov. synchronous registration of movement of left tegmen and sound (upper line: upward deflection indicating opening, downward closing; lower line: sound).
FIGURE 6 in Bioacoustics and systematics of Mecopoda (and related forms) from South East Asia and adjacent areas (Orthoptera, Tettigonioidea, Mecopodinae) including some chromosome data
FIGURE 6. Oscillograms of the calling songs of species of the Mecopoda niponensis subgroup and of M. cf. yunnana. Overview (12 s sections).
FIGURE 18 in Bioacoustics and systematics of Mecopoda (and related forms) from South East Asia and adjacent areas (Orthoptera, Tettigonioidea, Mecopodinae) including some chromosome data
FIGURE 18. Ovipositor of A Mecopoda angusta (CH3744) and B Eumecopoda platyphoea stat. nov., holotype. Scale 10 mm.
FIGURE 8 in Bioacoustics and systematics of Mecopoda (and related forms) from South East Asia and adjacent areas (Orthoptera, Tettigonioidea, Mecopodinae) including some chromosome data
FIGURE 8. Oscillograms of the calling songs of species of the Mecopoda confracta subgroup. Overview (12 s sections).
FIGURE 2 in Bioacoustics and systematics of Mecopoda (and related forms) from South East Asia and adjacent areas (Orthoptera, Tettigonioidea, Mecopodinae) including some chromosome data
FIGURE 2. Male subgenital plates in Mecopoda and Eumecopoda. A M. niponensis continentalis (CH7674), B M. niponensis vietnamica subsp. nov. (holotype), C M. himalaya (CH3737), D M. sismondoi sp. nov. (CH3738), E M. javana, neotype, F M. javana, Sri Lanka, G M. mahindai sp. nov., H E. cyrtoscelis zhantievi subsp. nov. Scale 2 mm.
FIGURE 16 in Bioacoustics and systematics of Mecopoda (and related forms) from South East Asia and adjacent areas (Orthoptera, Tettigonioidea, Mecopodinae) including some chromosome data
FIGURE 16. Frontal view of the head in Mecopoda and Eumecopoda species. A M. angusta, male, B M. angusta, female, C M. dilatata, male, syntype, D M. divergens, male, NMW, E M. divergens, female, holotype, F E. cyrtoscelis zhantievi subsp. nov., male, holotype.
FIGURE 13 in Bioacoustics and systematics of Mecopoda (and related forms) from South East Asia and adjacent areas (Orthoptera, Tettigonioidea, Mecopodinae) including some chromosome data
FIGURE 13. Mirror area in the right male tegmen of Mecopoda and Eumecopoda species. A–K: elongata-group: A–G niponensis-subgr.: A M. niponensis niponensis, lectotype, B M. niponensis vietnamica subsp. nov., holotype, C M. himalaya, Malaysia (CH3737), D M. macassariensis, holotype, E M. fallax, Thailand (CI 3254538), F M. s. stridulata (CRTmeceloM02), G M. s. stridulata (from Gorochov 2020), H niponensis-subgr.?: M. paucidens sp. nov., Java; I–L: confracta-subgr.: I M. sismondoi sp. nov., holotype, J M. javana, neotype, K M. javana, Sri Lanka, L M. mahindai sp. nov., holotype; M M. angusta, (CH3674), N Eumecopoda cyrtoscelis zhantievi subsp. nov., O M. dilatata, Borneo.
FIGURE 22 in Bioacoustics and systematics of Mecopoda (and related forms) from South East Asia and adjacent areas (Orthoptera, Tettigonioidea, Mecopodinae) including some chromosome data
FIGURE 22. File diversity in Mecopoda in selected areas. A Borneo, B Indonesian islands Sumatra-Java-Bali-Timor, C Thailand. Inter-tooth spacing in stridulatory files. Thick lines indicate specimens with known song. Red/lilac lines presumed niponensis subgroup, blue presumed confracta subgroup, green unknown, black paucidens. In the legend after specimen ID the number of stridulatory teeth and relative width of the mirror cells (width/length; in brackets).
FIGURE 12 in Bioacoustics and systematics of Mecopoda (and related forms) from South East Asia and adjacent areas (Orthoptera, Tettigonioidea, Mecopodinae) including some chromosome data
FIGURE 12. Inter-tooth spacing in stridulatory files of Mecopoda species. Thick lines and filled symbols indicate specimens with known song. A–D: M. elongata group: A M. niponensis subgroup and M. marmorata, B M. himalaya and macassariensis, C M. fallax and species with similar files, D M. confracta subgroup, E other Mecopoda and Eumecopoda species.
FIGURE 15. C in Bioacoustics and systematics of Mecopoda (and related forms) from South East Asia and adjacent areas (Orthoptera, Tettigonioidea, Mecopodinae) including some chromosome data
FIGURE 15. C-banded karyotypes (left side) and mitotic metaphase (right side) of five Mecopoda species with different chromosome number (2n). Karyotypes are reconstructed by arranging homologous chromosomes in order of decreasing size. X, sex chromosome.
FIGURE 21 in Bioacoustics and systematics of Mecopoda (and related forms) from South East Asia and adjacent areas (Orthoptera, Tettigonioidea, Mecopodinae) including some chromosome data
FIGURE 21. Distribution map of Eumecopoda species in and around Northwestern New Guinea. 1 type locality of E. cyrtoscelis zhantievi subsp. nov., 2 type locality of E. cyrtoscelis aru (Gorochov 2020, Redtenbacher 1892, Willemse 1933), 3–6 E. cyrtoscelis cyrtoscelis (3 type locality, 4 Hebard 1922, 5, 6 Helfert & Sänger 2007), 7–8 E. superba (7 Griffini 1908, Gorochov 2020, 8 type locality), 9–11 E. moluccarum (9 type locality, 10 Hebard 1922, 11 Gorochov 2020), 12 type locality of E. sp. spinosa Gorochov 2020, 13 type locality of E. spinosa supiori Gorochov 2020. Map based on SimpleMappr (Shorthouse, 2010).
FIGURE 1 in Bioacoustics and systematics of Mecopoda (and related forms) from South East Asia and adjacent areas (Orthoptera, Tettigonioidea, Mecopodinae) including some chromosome data
FIGURE 1. Mirror cells in the right male tegmen, viewed from the lower (A, C) and upper (B, D) side. A–B Mecopoda himalaya (CH3411), a member of the niponensis subgroup, C–D M. sismondoi sp. nov. (CH3688), confracta subgroup. Note the pretzel-shaped mirror in both species. Scale 5 mm.
Figure 1 in Chromosomal and genetic characterization of four Caribbean Prioninae (Coleoptera: Cerambycidae) species with notes on biogeography
Figure 1. Schematic representation of the Lesser Antilles and photography of the insects under study.
Figure 10 in Chromosomal and genetic characterization of four Caribbean Prioninae (Coleoptera: Cerambycidae) species with notes on biogeography
Figure 10. Phylogenetic tree resulting from the Bayesian analysis, clustering the different haplotypes of Prioninae retrieved from the Genbank with those assessed of this study as compressed subtree (red triangle). Expansion of the subtree and phylogenetic relationships between the different haplotypes is also shown. The topology of the clusters was similar for the UPGMA and NJ trees. Numbers above branches of the major clusters correspond to posterior probabilities from the Bayesian analysis. TdeH and TdeB: Terre-de-Haut and Terre-de-Bas islands from Les Saintes.
Figures 6-9 in Chromosomal and genetic characterization of four Caribbean Prioninae (Coleoptera: Cerambycidae) species with notes on biogeography
Figures 6-9. Karyotypes of Solenoptera and Hovorodon species. 6) Giemsa stained karyotype of S. touroulti exhibiting three pairs (# 1, 2 and 4) of sub-metacentric autosomes. 7) Karyotype of a spermatocyte I at pachynema of S. touroulti, after Giemsa (left) and silver (right) stainings. Notice the lack of synapsis at the NOR locus (arrow) and the silver staining of nucleoli. 8) Giemsa stained karyotype of H. maxillosum exhibiting 10 pairs of sub-metacentric autosomes. 9) Karyotype of a spermatocyte I at pachynema of H. maxillosum, after Giemsa (left) and silver (right) stainings. Arrow: NOR on bivalent 12. Bars = 10μm.
Figures 2-5 in Chromosomal and genetic characterization of four Caribbean Prioninae (Coleoptera: Cerambycidae) species with notes on biogeography
Figures 2-5. Karyotypes of Solenoptera species. 2) Giemsa stained male karyotype of S. canaliculata. The arrows on chromosome 4 indicate an elongated region, which is the only region stained by C-banding. Bar = 10 μm, as in other figures. 3) Karyotype of a spermatocyte I at pachynema of S. canaliculata, after Giemsa (left) and silver (right) stainings. The NOR on bivalent 4 looks elongated, and is surrounded by nucleoli after silver staining. 4) Giemsa stained XYY karyotype of S. quadrilineata. Chromosome 4 is elongated at the same position as in S. canaliculata (arrow), which indicates the position of the NOR. 5) Giemsa stained metaphase I of the XYY male of S. quadrilineata exhibiting a parachute sex trivalent. Arrows point out the two Ys. The accidental presence of two Ys in male beetles was estimated to about 1 per cent (Dutrillaux and Dutrillaux 2011). Bars = 10μm.
FIGURE 1. Snake chromosomes. A in Karyotypes of Coralsnakes (Reptilia: Elapidae) from the Western Hemisphere, with Comments on Intraspecific Variation and Centric Fission of Chromosomes
FIGURE 1. Snake chromosomes. A. Karyotype of Micruroides euryxanthus (2n = 34, with 14 macrochromosomes and 20 microchromosomes), AMNH R-109413, male. B. Karyotype of Micrurus tener (2n = 32 in males, 33 in females, with 16 macrochromosomes and 16 microchromosomes in males, 17 microchromosomes in females), AMNH R-110075, female illustrated with ZW1W2 sex chromosome heteromorphism. Scale bar = 10 µm.
Fig. 65 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 65. Evolution of carnivory inferred from our optimization of the carnivory character of Ferrarezi and Gimenez (1996: table 1; see our table 8) on our strict consensus tree from the character congruence analysis. The ''uncertain'' states for Phyllostomus and Tonatia are due to taxonomic polymorphism.
Fig. 64 in Phylogeny Of Phyllostomid Bats (Mammalia: Chiroptera): Data From Diverse Morphological Systems, Sex Chromosomes, And Restriction Sites
Fig. 64. Evolution of different types of nectarivory inferred from our optimization of the nectarivory character of Ferrarezi and Gimenez (1996: table 1; see our table 8) on our strict consensus tree from the character congruence analysis. Note that the nectarivory character, as defined by Ferrarezi and Gimenez (1996) includes the consumption of pollen and petals. To prevent an equivocal reconstruction for the base of the clade that includes all phyllostomids except desmodontines, we examined trees in which the position of Brachyphylla was resolved and fixed the node at the base of the clade that includes all phyllostomids except desmodontines with the state that occurred under the two alternative placements for this genus.
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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.