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FIGURE 11 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 11. Lateral view of dentate portion of right dentary (reversed) of Lobotes surinamensis, ASU 19554, 52 mm SL, showing alternative interpretations of tooth replacement: A) "grouped tooth replacement of Hilton & Bemis (2005), in which a functional group of lateral teeth (in blue) is replaced by the group of replacement teeth immediately basal to it (in pink); B) posterolateral tooth replacement, in which anteromedially directed series of teeth develop at their posterolateral end. The functional and replacement groups in A belong to two different series (shown, respectively, in yellow and red in B). Dark grey indicates non-mineralised portion of developing teeth. The circles below B show the relative positions of teeth when viewed dorsally. Illustrations by A.C. Gill.
FIGURE 10 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 10. Capros aper, cleared and stained 15 mm SL postflexion larva ZMUC P42227: A) whole specimen; B) detail of head to show serrations. Abbreviations: Aa, anguloarticular; Br, branchiostegals; Cl, cleithrum; Co, coracoid; D, dentary; F, frontal; IL, interopercle-mandibular ligament; IO1, infraorbital 1; LE, lateral ethmoid; Mx, maxilla; N, nasal; Pcl, postcleithra; PG, pelvic girdle; Pmx, premaxilla; Po, preopercle; Ptt, posttemporal; Ra, retroarticular; S, suproccipital; Scl, supracleithrum. Photos by A.C. Gill.
FIGURE 5. Larval Datnioides polota, 7.8 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 5. Larval Datnioides polota, 7.8 mm SL, AMS I.28986-046, from estuarine waters of the Malay Peninsula (after Ditty 2000: fig. 107). Illustration by J.M. Leis and S.B. Leis.
FIGURE 15 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 15. Lateral view of dentate portion of left dentary of Antigonia rhomboidea, AMS I.15526-006, 45 mm SL. Methods of presentation as in Figure 11B. Illustration by A.C. Gill.
FIGURE 13 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 13. Lateral view of posterior portion of left premaxilla of the chaetodontid Chaetodon auriga, ASU 19076, 63.0 mm SL. Methods of presentation as in Figure 11B, except circles represent ventral view of teeth in coloured series. Illustration by A.C. Gill.
FIGURE 1 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 1. Adult Lobotes surinamensis, ca. 150 mm SL, Swansboro, North Carolina, USA. Photo by A.K. Gardner.
FIGURE 9. Capros aper, 5.2 in Phylogenetic position of the fish genera Lobotes, Datnioides and Hapalogenys, with a reappraisal of acanthuriform composition and relationships based on adult and larval morphology
FIGURE 9. Capros aper, 5.2 mm SL postflexion larva ZMUC P42226, Dana 3529I. Spinule-shaped scales on nearly all of trunk and tail, including anterior to pelvic-fin base. These obscure the myomeres, which are omitted. A few spinule-shaped scales are also present on the cheek. A single spinule is at the base of each dorsal- and anal-fin element. The scales are shown only on a patch laterally on the upper trunk. Small spines on the fin spines are longer and more robust than the spinule-shaped scales. The dorsal tip of the ascending process of the premaxilla is dorsal to the posterior border of the nasal pit and hidden by the nasal ridge of spines. Pigment omitted. Scale bar = 1 mm. Illustration by J.M. Leis and S.B. Leis.
FIGURE 17 in Systematic position of Apodemia paucipuncta (Riodinidae), and a critical evaluation of the nymphidiine transtilla
FIGURE 17. Uncus in ventral view, gnathos in lateral view, and uncus plus tegumen and vinculum tip in dorsal view showing characters used in the analysis.
ECC-POPC-curved-bilayer-positive
<p>A curved POPC bilayer, restrained in the *negative* regions - positively curved regions are free to move.</p>
[Dataset] Tuneable reflexes control antennal positioning in flying hawkmoths
<p>The datasets used to study airflow-dependent antennal positioning in flying hawkmoths.</p>
Acoustic positioning telemetry in a case study on the Albert Canal (Belgium): VPS and YAPS positions
<p><strong>Description</strong><br> This dataset contains data of an acoustic positioning telemetry study on the Albert canal, in a 200x150 m area directly upstream of the navigation lock complex of Kwaadmechelen, Belgium. European silver eels (<em>Anguilla anguilla</em>) and Atlantic salmon smolts (<em>Salmo salar</em>) were tagged with 69-kHz acoustic transmitters (Vemco, Halifax, NS) and detected by acoustic receivers attached at the canal walls and ship guiding structures of the navigation lock complex. The study comprises 3 deployments between 2015-11-25 and 2017-06-16. At the end of each deployment, receivers were offloaded and the detections were sent to Vemco for processing and calculation of the VPS positions. Additionally, we used the raw detection data to calculate positions by use of the YAPS algorithm.</p> <p><strong>Files</strong></p> <ul> <li><strong>metadata.csv</strong>: definitions for the fields in deployments.csv, receivers.csv, transmitters.csv, detections.csv, positions_vps.csv, positions_yaps.csv and gps_track.csv.</li> <li><strong>deployments.csv</strong>: Start and end date of the 3 deployments. At the end of each deployment, receivers were offloaded and the detections were sent to Vemco for processing and calculation of the VPS positions.</li> <li><strong>receivers.csv</strong>: Positions and specifications of the used receivers (VR2W and 1 VRT2-x). Receivers with short_id ST8 and ST8-2 have the same receiver_id because it concerns the same receiver deployed in another position (changed on 2017-04-05 08:47). The short_id denotes this position.</li> <li><strong>transmitters.csv:</strong> Specifications of the used transmitters. Position and start_date/end_date are only specified for fixed transmitters (i.e. reference-Rx and synchronisation-Sx transmitters). S8-2, S9-2 and R4 were added during the last deployment, and have therefore start dates that differ from deployment start dates. Synchronisation transmitters Sx were collocated with receivers with corresponding STx-id. S8 and S8-2 have the same transmitter_id because it concerns the same transmitter deployed in another position.</li> <li><strong>detections.csv</strong>: Raw receiver detections with millisecond time accuracy, needed to perform the YAPS positioning algorithm. The synchronised time was calculated from the original time by use of the synchronisation transmitters: JennaVergeynst. (2019, November 13). JennaVergeynst/time_synchronization: Code for time synchronisation of an acoustic positioning system (Version v1.0.0). Zenodo. http://doi.org/10.5281/zenodo.3540681.</li> <li><strong>positions_vps.csv</strong>: Positions of fish, synchronisation and reference transmitters and test tracks from the Vemco Positioning System (VPS).</li> <li><strong>positions_yaps.csv</strong>: Positions of fish, synchronisation and reference transmitters and test tracks calculated with YAPS (Yet Another Positioning System): Baktoft, H., Gjelland, K. Ø., Økland, F., & Thygesen, U. H. (2017). Positioning of aquatic animals based on time‐of‐arrival and random walk models using YAPS (Yet Another Positioning Solver). Scientific Reports, 7(1), 14294. https://github.com/baktoft/yaps. The used code to prepare the synchronised detections as input data for YAPS, can be found on JennaVergeynst. (2019, November 13). JennaVergeynst/prepare_toa_for_yaps: Code to prepare TOA-data for YAPS (Version v1.0.0). Zenodo. http://doi.org/10.5281/zenodo.3540683</li> <li><strong>gps_track.csv</strong>: GPS positions of 2 test tracks: a track on 4 August with transmitter 255 and 53429 and one on 5 August with transmitter 16200.</li> </ul>
Figs 39–50 in On status and systematic position of Pterostichus goschi Jedlička, 1930 (Coleoptera: Carabidae)
Figs 39–50. Variation in the shape of the pronotum: 39–44 – Pterostichus neglectus A. Morawitz, 1862 (39 – Primorsky Krai, 18 km SW Barabash; 40 – Khabarovsky Krai, Khawar Stream below cordon Bichi; 41 – Primorsky Krai, Sikhote-Alinsky Reserve, bank of Lake Tsarskoye; 42 – Zabaykalsky Krai, Priargunsky district, Duroy; 43 – Khabarovsky Krai, stream between the 1st and 2nd Byk on Gorin River; 44 – Zabaykalsky Krai, Chita area, near Duroy); 45–50 – P. goschi Jedlička, 1930 (45 – Primorsky Krai, Cape Ostrovok Falshivy; 46 – Khabarovsky Krai, Namek Stream; 47 – Kunashir Island, forest lake 1 km above mouth of Tyatina River; 48 – Primorsky Krai, 1.7 km north of Cape L'va; 49, 50 – Primorsky Krai, Khasan environs). Рис. 39–50. ИЗменчивость формы переднеспинки: 39–44 — Pterostichus neglectus A. Morawitz, 1862 (39 — Приморский край, 18 км ЮЗ Барабаш; 40 — Хабаровский край, руч. Хавар ниЖе кордона Бичи; 41 — Приморский край, Сихоте-Алинский Заповедник, берег оЗ. Царское; 42 — Забайкальский край, Приаргунский р-н, Дурой; 43 — Хабаровский край, ручей меЖду 1-м и 2-м Быками на р. Горин; 44 — Забайкальский край, окрестности п. Дурой); 45–50 — P. goschi Jedlička, 1930 (45 — Приморский край, мыс Островок Фальшивый; 46 — Хабаровский край, ручей Намёк; 47 — Кунашир, лесное оЗеро 1 км выше устьЯ р. ТЯтина; 48 — Приморский край, 1,7 км севернее мыса Льва; 49, 50 — Приморский край, окрестности п. Хасан).
Figs 29–38 in On status and systematic position of Pterostichus goschi Jedlička, 1930 (Coleoptera: Carabidae)
Figs 29–38. Male of Pterostichus (Badistrinus) from Khasan district, detals: 29–30, 33–35 — P. goschi Jedlička, 1930; 31–32, 36– 38 — P. neglectus A. Morawitz, 1862; 29, 31 — dorsal habitus; 30, 32 — hind angle of pronotum; 33–38 — aedeagus, lateral and dorsal view. Рис. 29–38. Детали строениЯ самцов of Pterostichus (Badistrinus) иЗ Хасанского района: 29–30, 33–35 — P. goschi Jedlička, 1930; 31–32, 36–38 — P. neglectus A. Morawitz, 1862; 29, 31 — внешний вид, сверху; 30, 32 — Задние углы переднеспинки; 33–38 — Эдеагус, сбоку и сверху.
Figs 19–20. Pterostichus neglectus A. Morawitz, 1862 in On status and systematic position of Pterostichus goschi Jedlička, 1930 (Coleoptera: Carabidae)
Figs 19–20. Pterostichus neglectus A. Morawitz, 1862, lectotype, male: 19 — dorsal habitus; 20 — labels. Рис. 19–20. Pterostichus neglectus A. Morawitz, 1862, лектотип, самец: 19 — вид сверху; 20 — Этикетки.
Figs 21–28 in On status and systematic position of Pterostichus goschi Jedlička, 1930 (Coleoptera: Carabidae)
Figs 21–28. Endophallus: 21–24 — Pterostichus neglectus A. Morawitz, 1862 (Khabarovsky Krai, Khawar Stream below cordon Bichi); 25–28 — P. goschi Jedlička, 1930 (25 — Nikolsk Ussurijsk, lectotype; 26 — Kunashir, forest lake 1 km above mouth of Tyatina River; 27 — Primorsky Krai, Cape Ostrovok Falshivy; 28 — Khabarovsky Krai, Namek Stream); 21 — left view; 22 — dorsal view; 23, 25–28 — ventral view; 24 — right view. Рис. 21–28. Эндофаллус: 21–24 — Pterostichus neglectus A. Morawitz, 1862 (Хабаровский край, ручей Хавар ниЖе кордона Бичи); 25–28 — P. goschi Jedlička, 1930 (25 — Уссурийск [Nikolsk Ussurijsk], лектотип; 26 — Кунашир, лесное оЗеро 1 км выше устьЯ р. ТЯтина; 27 — Приморский край, мыс Островок Фальшивый; 28 — Хабаровский край, ручей Намёк); 21 — слева; 22 — сверху; 23, 25–28 — сниЗу; 24 — справа.
Figs 4–8 in On status and systematic position of Pterostichus goschi Jedlička, 1930 (Coleoptera: Carabidae)
Figs 4–8. Pterostichus goschi Jedlička, 1930, lectotype, male genitalia: 4 — aedeagus, left view; 5 — same, right view; 6 — same, dorsal view; 7 — right paramere; 8 — left paramere. Рис.4–8. Pterostichus goschi Jedlička, 1930, лектотип, гениталии самца: 4 — Эдеагус, слева; 5 — то Же, справа; 6 — то Же, сверху; 7 — праваЯ парамера; 8 — леваЯ парамера.
Fig. 1 in The phylogenetic position of Neogosseidae (Gastrotricha: Chaetonotida) and the origin of planktonic Gastrotricha
Fig. 1 Species of Neogosseidae included in this study. a Kijanebalola devestiva, habitus of adult specimen. Note the rounded posterior end with single median group of spines. b Neogossea acanthocolla, habitus of adult specimen. Note the truncate posterior end with a pair of tufts. c Neogossea antennigera, anterior two thirds of body of adult specimen. d N. antennigera, posterior end of body of adult specimen. Note the truncate posterior end with a pair of tufts. Scale bars: a and b, 50 μm; c and d, 25 μm
Fig. 2 in Hypotheses on rostral shield evolution in fossorial lizards derived from the phylogenetic position of a new species of Paracontias (Squamata, Scincidae)
Fig. 2 Phylogenetic tree of Malagasy Scincinae recon- structed using Bayesian inference (20 Mio. generations; trees sampled every 1000 generations; burn-in 10,000), based on 3,936 bp DNA sequences of 12S and 16S rRNA, ND1, BDNF, Rag2, Cmos, Enol and phosducin. Legless fossorial lineages highlighted in grey. Cordylus, Tiliqua and 'Eumeces' sensu lato used as out-group (not shown). Numbers at nodes are Bayesian posterior probabilities followed by bootstrap support values>50% from Maximum Parsimony analysis (10,000 replicates)
Fig. 4 in Hypotheses on rostral shield evolution in fossorial lizards derived from the phylogenetic position of a new species of Paracontias (Squamata, Scincidae)
Fig. 4 Live habitus of holotypes of Paracontias vermisaurus sp. n. a and P. hafa b. Photographs by M. Vences and F. Andreone, respectively
Fig. 6 Miracopteron mirabile Novokshonov, 1993 in On the phylogenetic position of the palaeopteran Syntonopteroidea (Insecta: Ephemeroptera), with a new species from the Upper Carboniferous of England
Fig. 6 Miracopteron mirabile Novokshonov, 1993, holotype (No. 2/ 135, Paleontological Institute, Russian Academy of Sciences, Moscow); photograph of counterpart. Scale bar 10 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
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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
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