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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 3 in Assessing the taxonomic status of tropical frogs through bioacoustics: geographical variation in the advertisement calls in the Eleutherodactylus discoidalis species group (Anura)
Figure 3. Discriminant function analyses of the number of pulses, call length, and dominant frequency of species belonging to the Eleutherodactylus discoidalis group. Ellipses only intend to facilitate the observation of groups. BV, Eleutherodactylus cf. cruralis from the Bellavista Mountains; EC, Eleutherodactylus cruralis; ED, Eleutherodactylus discoidalis; EI, Eleutherodactylus ibischi; HO, Eleutherodactylus cf. cruralis from La Hoyada; EM, Eleutherodactylus madidi.
Figure 2 in Assessing the taxonomic status of tropical frogs through bioacoustics: geographical variation in the advertisement calls in the Eleutherodactylus discoidalis species group (Anura)
Figure 2. Oscillogram and sound spectrogram of the advertisement call of: (A) Eleutherodactylus cruralis from Rurrenabaque, Amazonian rainforest; (B) E. cf. cruralis from Bellavista Mountains; (C) E. cf. cruralis from La Hoyada; (D) Eleutherodactylus discoidalis from Campos de Pinos; (E) Eleutherodactylus ibischi from Samaipata Road; (F) Eleutherodactylus madidi from Eslabón.
Figure 4 in Assessing the taxonomic status of tropical frogs through bioacoustics: geographical variation in the advertisement calls in the Eleutherodactylus discoidalis species group (Anura)
Figure 4. Scatterplot for (A) number of pulses and call length, (B) dominant frequency and number of pulses, and (C) dominant frequency and call length of species and populations of the Eleutherodactylus discoidalis group. Lines correspond to normally distributed probability ellipses (0.99, N = 194). BV, Eleutherodactylus cf. cruralis from the Bellavista Mountains; EC, Eleutherodactylus cruralis; ED, Eleutherodactylus discoidalis; EI, Eleutherodactylus ibischi; HO, Eleutherodactylus cf. cruralis from La Hoyada; EM, Eleutherodactylus madidi.
Figure 1 in Assessing the taxonomic status of tropical frogs through bioacoustics: geographical variation in the advertisement calls in the Eleutherodactylus discoidalis species group (Anura)
Figure 1. Map of the Andes of Bolivia showing the studied localities (see also Table 1). 1, Eslabón; 2, Chalalán; 3, Rurrenabaque; 4, Chapare, 500 m; 5, Mataracú; 6, La Hoyada; 7, Samaipata road; 8, Bellavista Mt; 9, Masicurí; 10, Campos de Pinos.
FIGURE 78 in An inordinate fondness for inconspicuous brown frogs: integration of phylogenomics, archival DNA analysis, morphology, and bioacoustics yields 24 new taxa in the subgenus Brygoomantis (genus Mantidactylus) from Madagascar
FIGURE 78. Mantidactylus manerana fotaka ssp. nov. in life. (a,b) Adult female from Sorata in dorsolateral and ventral view. Specimen probably corresponding to a voucher deposited in the UADBA collection.
FIGURE 77 in An inordinate fondness for inconspicuous brown frogs: integration of phylogenomics, archival DNA analysis, morphology, and bioacoustics yields 24 new taxa in the subgenus Brygoomantis (genus Mantidactylus) from Madagascar
FIGURE 77. Audiospectrogram and corresponding oscillogram of one advertisement call of the holotype of Mantidactylus manerana manerana, recorded on 17 November 2016 at Camp Simpona, Marojejy National Park (ca 20°C air temperature). Recording bandpass-filtered at 350–6000 Hz.
FIGURE 76 in An inordinate fondness for inconspicuous brown frogs: integration of phylogenomics, archival DNA analysis, morphology, and bioacoustics yields 24 new taxa in the subgenus Brygoomantis (genus Mantidactylus) from Madagascar
FIGURE 76. Mantidactylus manerana manerana sp. nov. from Marojejy in life, in dorsolateral and ventral view. (a,b) Adult male (holotype ZSM 500/2016 = ZCMV 15162), photographed in 2016. (c,d). Adult male (ZSM 209/2005 = FGZC 2881), photographed in 2005. (e,f) Adult male (ZSM 207/2005 = FGZC 2846), photographed in 2005.
FIGURE 73 in An inordinate fondness for inconspicuous brown frogs: integration of phylogenomics, archival DNA analysis, morphology, and bioacoustics yields 24 new taxa in the subgenus Brygoomantis (genus Mantidactylus) from Madagascar
FIGURE 73. Preserved lectotype of Mantidactylus inaudax, and holotype specimens of newly named species and subspecies in the M. inaudax clade. Scale bars equal 5 mm.
FIGURE 71 in An inordinate fondness for inconspicuous brown frogs: integration of phylogenomics, archival DNA analysis, morphology, and bioacoustics yields 24 new taxa in the subgenus Brygoomantis (genus Mantidactylus) from Madagascar
FIGURE 71. Audiospectrogram and corresponding oscillogram of a 1000 ms section of a series of advertisement calls (three calls figured) tentatively allocated to Mantidactylus glosi, recorded on 26 February 2006 at Ambatovory (air temperature not measured). Recording bandpass-filtered at 640–2300 Hz.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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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.