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Figure 3 from: Short M (2015) New records of Lophoproctus coecus Pocock, 1894 (Diplopoda, Polyxenida, Lophoproctidae) extend the range of the genus Lophoproctus. In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 209-222. https://doi.org/10.3897/zookeys.510.8668
Figure 3 - Lophoproctus coecus (Pocock, 1888), Krasnodar Province, Russia. Illustration of diagnostic features. A labrum showing triangular median linguiform process B typical setae on coxa C right antenna showing articles VI–VIII with sensilla D right antennal article VI showing arrangement of sensilla E tarsus 2 and telotarsus. Scale bars: 10 µm (A, B); 50 µm (C); 20 µm (D, E).
Figure 2 from: Short M (2015) New records of Lophoproctus coecus Pocock, 1894 (Diplopoda, Polyxenida, Lophoproctidae) extend the range of the genus Lophoproctus. In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 209-222. https://doi.org/10.3897/zookeys.510.8668
Figure 2 - Typical pattern of basiconic sensilla on the right 6th antennal article. A Lophoproctus coecus B Lophoproctus lucidus. The coeloconic sensilla are not visible due to angle of view. Scale bar: 20 µm (A, B).
Figure 2 from: Tuf IH, Chmelík V, Dobroruka I, Hábová L, Hudcová P, Šipoš J, Stašiov S (2015) Hay-bait traps are a useful tool for sampling of soil dwelling millipedes and centipedes. In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 197-207. https://doi.org/10.3897/zookeys.510.9020
Figure 2 - Changes in myriapod communities inside hay-bait traps installed in three biotopes during the 12 week trapping period. Qualitative as well as quantitative parameters are shown for these communities. Open dots are observed parameters, whereas solid lines represent models of succession including standard errors (green shading).
Figure 1 from: Short M (2015) New records of Lophoproctus coecus Pocock, 1894 (Diplopoda, Polyxenida, Lophoproctidae) extend the range of the genus Lophoproctus. In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 209-222. https://doi.org/10.3897/zookeys.510.8668
Figure 1 - Habitus drawing of Lophoproctus coecus Pocock, 1894 showing typical morphology of the family Lophoproctidae.
Figure 1 from: Tuf IH, Chmelík V, Dobroruka I, Hábová L, Hudcová P, Šipoš J, Stašiov S (2015) Hay-bait traps are a useful tool for sampling of soil dwelling millipedes and centipedes. In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 197-207. https://doi.org/10.3897/zookeys.510.9020
Figure 1 - Rarefactions of estimated species richness (i.e. number of species) in increasing size of random samples (i.e. number of individuals), comparison of effectiveness of sampling by individual methods at different sites. Vertical lines represent standard errors.
Figure 3 from: Bogyó D, Magura T, Nagy DD, Tóthmérész B (2015) Distribution of millipedes (Myriapoda, Diplopoda) along a forest interior – forest edge – grassland habitat complex. In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 181-195. https://doi.org/10.3897/zookeys.510.8657
Figure 3 - DCCA analysis for the millipede species of the study area. Squares represent the sampled habitats (blue squares: samples from the forest interior habitat; red squares: samples from the forest edge habitat; black squares: samples from the grassland habitat).The arrows denote the increase of the value of the environmental variables (airtemp: air temperature on the surface; canopy: canopy cover; DH: soil dehydrogenase enzyme activity; dwood: cover of decaying wood material; herbs: cover of herbs; littcover: cover of leaf litter; littdepth: depth of leaf litter; humidity: relative humidity on the surface; pH: soil pH; shrubs: cover of shrubs; stemp: soil temperature at 2cm depth; smoisture: soil moisture; woodysp: number of woody plant species). Green circles and the four-letter abbreviations indicate the millipede species (BRBA: Brachyiulus bagnalli; BRSU: Brachydesmus superus; GLTE: Glomeris tetrasticha; JUTE: Julus terrestris; KROC: Kryphioiulus occultus; LECI: Leptoiulus cibdellus; MABO: Mastigona bosniensis; MEUN: Megaphyllum unilineatum; POCO: Polydesmus complanatus).
Figure 2 from: Bogyó D, Magura T, Nagy DD, Tóthmérész B (2015) Distribution of millipedes (Myriapoda, Diplopoda) along a forest interior – forest edge – grassland habitat complex. In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 181-195. https://doi.org/10.3897/zookeys.510.8657
Figure 2 - Hierarchical cluster analysis of millipede assemblages of the studied habitats using Hellinger distance and Ward fusion method.
Figure 1 from: Bogyó D, Magura T, Nagy DD, Tóthmérész B (2015) Distribution of millipedes (Myriapoda, Diplopoda) along a forest interior – forest edge – grassland habitat complex. In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 181-195. https://doi.org/10.3897/zookeys.510.8657
Figure 1 - Millipede abundance, species richness and Shannon diversity at the studied habitats. Mean values (±SD) of the overall millipede abundance (A), species richness (B) and Shannon diversity (C) per samples at the studied habitats. Different letters indicate significant differences by Tukey test.
Figure 1 from: Leśniewska M, Jastrzębski P, Stańska M, Hajdamowicz I (2015) Centipede (Chilopoda) richness and diversity in the Bug River valley (Eastern Poland). In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 125-139. https://doi.org/10.3897/zookeys.510.8763
Figure 1 - Location of the study area in Poland. Study area. Morzyczyn, Płatkownica – lower section of the Bug valley: Mogielnica, Zabuże, Gnojno – central section of the Bug valley.
Figure 4 from: Papastefanou G, Panayiotou E, Mylonas M, Simaiakis SM (2015) Centipede assemblages along an urbanization gradient in the city of Heraklion, Crete (Greece). In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 163-179. https://doi.org/10.3897/zookeys.510.8414
Figure 4 - NMDS two-dimensional ordination plot based on the Bray-Curtis dissimilarity matrix of the nine sites along the urbanization gradient.
Figure 9 from: Golovatch SI (2015) Cave Diplopoda of southern China with reference to millipede diversity in Southeast Asia. In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 79-94. https://doi.org/10.3897/zookeys.510.8640
Figure 9 - Distribution of Pacidesmus species. After Golovatch and Geoffroy (2014). Map courtesy L. Deharveng & A. Bedos.
Figures 3-6 from: Stoev P, Akkari N, Komerički A, Edgecombe GD, Bonato L (2015) At the end of the rope: Geophilus hadesi sp. n. – the world's deepest cave-dwelling centipede (Chilopoda, Geophilomorpha, Geophilidae). In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 95-114. https://doi.org/10.3897/zookeys.510.9614
Figures 3-6 - Geophilus hadesi sp. n. 3 cephalic capsule, dorsal 4 clypeus, ventral 5 right antenna, article IV, dorsal 6a right antenna, ultimate articles, dorsal 6b right antenna, close up of sensilla basiconica cluster, mesal. SEM micrographs taken from female paratype NHMW8363 from cave Muda labudova.
Figures 2-4 from: Golovatch SI (2015) Cave Diplopoda of southern China with reference to millipede diversity in Southeast Asia. In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 79-94. https://doi.org/10.3897/zookeys.510.8640
Figures 2-4 - Habitus of Nepalella grandoides Golovatch, Geoffroy & Mauriès, 2006, a completely unpigmented, blind, long-legged and long-antenned troglobiont from Sichuan, length nearly 38 mm. After Golovatch et al. (2006b). Photos courtesy L. Albenga.
Figures 7-10 from: Stoev P, Akkari N, Komerički A, Edgecombe GD, Bonato L (2015) At the end of the rope: Geophilus hadesi sp. n. – the world's deepest cave-dwelling centipede (Chilopoda, Geophilomorpha, Geophilidae). In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 95-114. https://doi.org/10.3897/zookeys.510.9614
Figures 7-10 - Geophilus hadesi sp. n. 7 intermediate part of labrum, ventral 8 right half of the maxillary complex, ventral 9 forcipular segment, ventral 10 close up of forcipular coxosternite, ventral. SEM micrographs taken from female paratype NHMW8363 from cave Muda labudova. Abbreviations: labral bristle (lb), labral denticle (ld), first maxillae (MxI), second maxillae (MxII), first maxillary telopodite (tl), first maxillary coxal projection (cxp), second maxillary pretarsus (p), coxopleural suture (cxps), chitin-line (chl), basal denticle of tarsungulum (bd).
Figure 20 from: Stoev P, Akkari N, Komerički A, Edgecombe GD, Bonato L (2015) At the end of the rope: Geophilus hadesi sp. n. – the world's deepest cave-dwelling centipede (Chilopoda, Geophilomorpha, Geophilidae). In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 95-114. https://doi.org/10.3897/zookeys.510.9614
Figure 20 - Ultimate leg-bearing segment and postpedal segments, ventral. Photo taken from female paratype NHMW8363 from cave Muda labudova.
Figure 2 from: David J-F, Coulis M (2015) Millipedes faced with drought: the life cycle of a Mediterranean population of Ommatoiulus sabulosus (Linnaeus) (Diplopoda, Julida, Julidae). In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 115-124. https://doi.org/10.3897/zookeys.510.8838
Figure 2 - Phenology of Ommatoiulus sabulosus in Provence (March 2010–November 2010). See explanations in the legend to Fig. 1.
Figure 1 from: Golovatch SI (2015) Cave Diplopoda of southern China with reference to millipede diversity in Southeast Asia. In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 79-94. https://doi.org/10.3897/zookeys.510.8640
Figure 1 - Main trends in the ecological evolution of Diplopoda. All are life forms except for arboricoles. 1 stratobionts 2 trunk and crown arboricoles, as well as subcorticolous xylobionts 3 epiphytobionts 4 troglobionts 5 geobionts. NB: The thickness of numbered arrows roughly corresponds to the share of the respective ecological grouping along a gradient of biome succession with age (uppermost arrows, the gap between them indicates the primary subtropical biome whence developed all the main extant biomes). After Kime and Golovatch (2000). Drawing courtesy S. Dashdamirov.
Figure 1 from: Edgecombe GD, Vahtera V, Giribet G, Kaunisto P (2015) Species limits and phylogeography of Newportia (Scolopendromorpha) and implications for widespread morphospecies. In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 65-77. https://doi.org/10.3897/zookeys.510.8573
Figure 1 - Map of Mesoamerica, the Caribbean and northern South America showing geographic distribution of Newportia specimens analyzed herein (see Table 1 for coordinates of samples).
Figure 5 from: Oeyen JP, Wesener T (2015) Steps towards a phylogeny of the pill millipedes: non-monophyly of the family Protoglomeridae, with an integrative redescription of Eupeyerimhoffia archimedis (Diplopoda, Glomerida). In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 49-64. https://doi.org/10.3897/zookeys.510.8675
Figure 5 - Eupeyerimhoffia archimedis (Strasser, 1965) male and female, SEM. A Leg-pair 1, male, right side, posterior view B Leg-pair 2, female, right side, posterior view C Leg-pair 2, male, left side, posterior view D Leg-pair 2, female, right vulva, ventral view E Leg-pair 2, male gonopore, posterior view F Leg-pair 9, male, right side, posterior view G Leg-pair 17, left side, anterior view H Leg-pair 18, right side, posterior view I Telopod with syncoxite, anterior view J Telopod, inner horn of syncoxite K Telopod, posterior view. Abbreviations: Cx = Coxa; Pre = Prefemur; Fem = Femur; Post = Postfemur; Tib = Tibia; Tar = Tarsus; Vu = Vulva; Go = Gonopore; Mp = Median plate; Lp = Lateral plate; Op = Operculum; 1-4 = Podomere 1-4; cL = Central lobe; h = Inner horn; Scx = Syncoxite; Tr = Trichostele. Scale bar: 400 μm (A, B); 250 μm (C); 100 μm (D, H); 25 μm (E); 200 μm (F, I); 150 μm (G, K); 50 μm (J).
Figure 4 from: Oeyen JP, Wesener T (2015) Steps towards a phylogeny of the pill millipedes: non-monophyly of the family Protoglomeridae, with an integrative redescription of Eupeyerimhoffia archimedis (Diplopoda, Glomerida). In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 49-64. https://doi.org/10.3897/zookeys.510.8675
Figure 4 - Eupeyerimhoffia archimedis (Strasser, 1965) male, SEM. A Thoracic shield, dorso-lateral view B Thoracic shield, meso-lateral C Thoracic shield, schism detail, ventro-lateral view D Tergite, detail of peg, antero-lateral view E Tergite, detail of depression, lateral view F Tergite, ventral view G Tergite, dorso-lateral view H Tergite, ozopore, dorsal view I Collum, dorsal view J Tergite 11 and anal shield, detail of furrow, ventro-lateral view K Tergite 11 and anal shield, left side, anterior view L Tergite 11 and anal shield, right side, posterior view. Abbreviations: AS = Anal shield; Dp = Depression; F = Furrow; Oz = Ozopore; LDp = Lateral depression; P = Peg; Sch = Schisma; stri = striae; T11 = Tergite 11. Arrows point anteriorly. Scale bar: 400 μm (A, H, I, K, L); 300 μm (B, F); 100 μm (C, D, J); 50 μm (E); 500 μm (G).
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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)
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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.