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Text-fig. 4. Ratio diagrams of total length of p3–m3. Parasorex depereti from BRS 25 (data from Fanfani 1999), Parasorex depereti (data from Crochet 1986), Parasorex ibericus, type locality Otura-1, Spain (Mein and Martín-Suárez 1993), Parasorex pristinus (Ziegler 2003), Apulogalerix pusillus, Gargano (fissure filling F32), Italy (Masini and Fanfani 2013). On the horizontal axis are reported the element of the series, in ordinates the ratio of the average lengths on the standard Parasorex socialis from La Grive, France (data from Masini and Fanfani 2013). in New Light On Parasorex Depereti (Erinaceomorpha: Erinaceidae: Galericini) From The Late Messinian (Mn 13) Of The Monticino Quarry (Brisighella, Faenza, Italy)
Text-fig. 4. Ratio diagrams of total length of p3–m3. Parasorex depereti from BRS 25 (data from Fanfani 1999), Parasorex depereti (data from Crochet 1986), Parasorex ibericus, type locality Otura-1, Spain (Mein and Martín-Suárez 1993), Parasorex pristinus (Ziegler 2003), Apulogalerix pusillus, Gargano (fissure filling F32), Italy (Masini and Fanfani 2013). On the horizontal axis are reported the element of the series, in ordinates the ratio of the average lengths on the standard Parasorex socialis from La Grive, France (data from Masini and Fanfani 2013).
Figs 13-18 in New data on the Afrotropical Xantholinini. 1. New species from South Africa in the Janak collection (Coleoptera, Staphylinidae) 285° contribution to the knowledge of the Staphylinidae
Figs 13-18: Tergite and sternite of the male genital segment, aedeagus of Notolinopsis khoi nov.sp. (13-15) and Notolinopsis lemniscatus nov.sp. (16-18) (scale bar: 0.1 mm).
Figs 7-12 in New data on the Afrotropical Xantholinini. 1. New species from South Africa in the Janak collection (Coleoptera, Staphylinidae) 285° contribution to the knowledge of the Staphylinidae
Figs 7-12: Tergite and sternite of the male genital segment, aedeagus of Notolinopsis mbotyianus nov.sp. (7-9) and Notolinopsis mirabilis nov.sp. (10-12) (scale bar: 0.1 mm).
Figs 1-6 in New data on the Afrotropical Xantholinini. 1. New species from South Africa in the Janak collection (Coleoptera, Staphylinidae) 285° contribution to the knowledge of the Staphylinidae
Figs 1-6: Tergite and sternite of the male genital segment, aedeagus of Xanthophius janaki nov.sp. (1-3) and Notolinopsis janaki nov.sp. (4-6) (scale bar: 0.1 mm).
Fig. 3-4 in Description of a new Nebria (Eunebria) species from Iran (Coleoptera, Carabidae: Nebriini) and faunistic data for Nebria (Eunebria) xanthacra xanthacra CHAUDOIR, 1850
Fig. 3-4: waterfall at Darb-e Āsīāb vill. (3) canyon above type locality. (4) type locality (photograph: D.W.W.).
Figs 5-8 in Description of a new Nebria (Eunebria) species from Iran (Coleoptera, Carabidae: Nebriini) and faunistic data for Nebria (Eunebria) xanthacra xanthacra CHAUDOIR, 1850
Figs 5-8: Nebria, 5, 6, 8: N. kazemii nov.sp. 7: N. xanthacra xanthacra CHAUDOIR. 5, 5a: median lobe of aedeagus. (5) lateral view (holotype). (5a) dorsal view (median lobe without base, paratype) (scale bar 1 mm). 6-8: female genitalia. (6) left apical gonocoxite of ovipositor, ventral view (paratype). 7, 8: female genital tract. (7) N. xanthacra xanthacra CHAUDOIR (waterfall at Darb-e Āsīāb vill.). (8) N. kazemii nov.sp. (paratype). dbs: dorsal bursal sclerite; sp: spermatheca; spd: spermathecal duct (scale bar 1 mm).
Figs 1, 2 in Description of a new Nebria (Eunebria) species from Iran (Coleoptera, Carabidae: Nebriini) and faunistic data for Nebria (Eunebria) xanthacra xanthacra CHAUDOIR, 1850
Figs 1, 2: Nebria, habitus. (1) N. kazemii nov.sp. (paratype). (2) N. boiteli ALL. (Moyen Atlas, Lac Sidi Ali).
Fig. 1 in New data on Vespid wasp fauna of Jordan (Hymenoptera, Vespidae)
Fig. 1: Position of localities under study. For localities numbers see the chapter "List of localities".
Figure 4 in Mideopsis milankovici sp. nov. a new water mite from Montenegro based on morphological and molecular data (Acariformes, Hydrachnidia, Mideopsidae)
Figure 4 Photographs of dorsal shield (a–d; photographed immediately after dissection) and ejaculatory complex (e–g). a–c, e– Mideopsisg, milankovici sp. nov., Međurječka Rijeka stream, Montenegro: a, e, f – holotype ♂; b, g – paratype ♂; c – paratype ♀. d –M. persicus Pešić & Saboori, 2015, holotype ♂, Firooz Abad, Iran. Scale bar = 100 µm.
Figure 2 in Mideopsis milankovici sp. nov. a new water mite from Montenegro based on morphological and molecular data (Acariformes, Hydrachnidia, Mideopsidae)
Figure 2 Mideopsis milankovici sp. nov., ♂ (a–c, e, holotype; d, paratype), Međurječka rijeka stream, Montenegro. a – dorsal shield; b – ventral shield; c–d, ejaculatory complex; e – palp. Scale bars = 100 µm.
Figure 1 in Mideopsis milankovici sp. nov. a new water mite from Montenegro based on morphological and molecular data (Acariformes, Hydrachnidia, Mideopsidae)
Figure 1 Maximum Likelihood tree based on the barcode region of the COI marker. The numbers near the branches represent the bootstrap probabilities.
Figure 5 in Mideopsis milankovici sp. nov. a new water mite from Montenegro based on morphological and molecular data (Acariformes, Hydrachnidia, Mideopsidae)
Figure 5 Međurječka Rijeka stream, the locus typicus of Mideopsis milankovici sp. nov. (inset). Photo by V. Pešić.
FIG. 5 in New data on embryonic development of Halisarca dujardini Johnston, 1842 (Demospongiae, Halisarcida)
FIG. 5. — Scheme of H. dujardini embryonic development; A, mature egg; B, early cleavage; C, beginning of blastomere polarization; D, multipolar immigration; E, stage larval polarization; F, formation of internal sphere and migration of maternal eosinophilic granular amoebocytes into larva; G, disphaerula, larva of H. dujardini. Abbreviations: bi, blastocoel; ec, embryonic capsule; efa, eosinophilic amoebocytes; ic, internal cells; isp, internal sphere; mc, migrated cells; ppc, posterior pole cells; tc, transition cells; yg, yolk granules.
FIG. 4. — A in New data on embryonic development of Halisarca dujardini Johnston, 1842 (Demospongiae, Halisarcida)
FIG. 4. — A, internal flagellate cells of disphaerula; B, flagellated cell that migrated from internal sphere. Abbreviations: f, flagellum; isc, internal sphere cavity; n, nucleus; yg, yolk granules; ba, bacteria. Scale bars: A, 4 µm; B, 1 µm.
FIG. 3. — A in New data on embryonic development of Halisarca dujardini Johnston, 1842 (Demospongiae, Halisarcida)
FIG. 3. — A, division of external flagellate cells in prelarva; B, maternal eosinophilic granular amoebocyte between internal cells of disphaerula; C, posterior pole of larva; D, external flagellate epithelium of larva. Abbreviations: ba, bacteria; ic, internal cells; ec, embryonic capsule; ppc, posterior pole cells; tc, transition cells; dc, divided cell; ecc, embryonic capsule cell; f, flagellum; n, nucleus; yg, yolk granules. Scale bars: A, 5 µm; B, 5 µm; C, 10 µm; D, 5 µm.
FIG. 2. — A in New data on embryonic development of Halisarca dujardini Johnston, 1842 (Demospongiae, Halisarcida)
FIG. 2. — A, cleaving embryos in 8-cell stage; B, blastula after immigration of external cells; C, stage of invagination of flagellate cells forming internal sphere; D, disphaerula of H. dujardini. Abbreviations: ec, embryonic capsule; ic, internal cells; n, nucleus; efc, external flagellate cells; b, blastomere; bi, blastocoel; ifc, internal flagellate cells; is, internal sphere; ppc, posterior pole cells; tc, transition cells. Scale bars: A, 20 µm; B, 15 µm; C, 20 µm; D, 10 µm.
Figure 20 in The interrelationships of Devonian lungfishes (Sarcopterygii: Dipnoi) as inferred from neurocranial evidence and new data from the genus Soederberghia Lehman, 1959
Figure 20. Unambiguous character changes mapped on one possible resolution of the clade above Stomiahykus and Uranolophus found among the 72 most parsimonious cladograms (tree statistics with no character ordering implemented: L = 125, CI = 0.5760, RI = 0.8094, RCI = 0.4662) retrieved from analysis of data derived from the neurocranial complex. This topology places Melanognathus in a basal position relative to that shown in Figure 21, as the sister taxon of all lungfishes with the exception of Dipnorhynchus, Uranolophus and Speonesdyrion.
Figure 7 in The interrelationships of Devonian lungfishes (Sarcopterygii: Dipnoi) as inferred from neurocranial evidence and new data from the genus Soederberghia Lehman, 1959
Figure 7. Soederberghia groenlandica, visceral surface of dermal skull roof with endoskeletal ossifications of the ethmoid region (MGUH VP 28398). Anterior is to the top. A, specimen photograph; B, interpretive drawing. Light grey shading in B corresponds to areas of matrix with bone impressions, while dark grey regions represent matrix. Diagonal hatching indicates damaged bone surface. Scale bar represents 20 mm.
Figure 24 in The interrelationships of Devonian lungfishes (Sarcopterygii: Dipnoi) as inferred from neurocranial evidence and new data from the genus Soederberghia Lehman, 1959
Figure 24. Distribution of cladogram lengths for the neurocranial data set for 1 × 108 randomly generated topologies. Arrow marked with MPT indicates the length of the shortest tree for the neurocranial data set (L = 125), while that marked with CB indicates the length of the shortest tree returning a topology consistent with the three-lineage scheme of Campbell & Barwick (1990; L = 143). These two cladograms are considerably shorter than most possible topologies, falling within the far left tail of the treelength distribution (the shortest 5% of all trees fall to the left of the dashed line marked with 95%). All other constrained topologies examined in this paper (monophyletic Chirodipterus: L = 137; monophyletic 'Chirodipteridae': L = 132; [Holodipterus + Griphognathus]: L = 133; monophyletic Griphognathus: L = 130) lie between the two arrows.
Figure 11 in The interrelationships of Devonian lungfishes (Sarcopterygii: Dipnoi) as inferred from neurocranial evidence and new data from the genus Soederberghia Lehman, 1959
Figure 11. Palatal bones of fleurantiid lungfishes. Anterior is to the top in both figures. A, interpretive drawing of the palate of Fleurantia denticulata in dorsal view (BMNH P24748); B, specimen photograph of the parasphenoid of Jarvikia arctica in ventral view (MGUH VP 28401). Scale bar represents 10 cm.
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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.