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Figures 14–18 in Species of the genus Steganopsis from China (Diptera: Lauxaniidae)
Figures 14–18. Stegonopsis multilineata de Meijere, 1924, male. 14. Syntergosternite and epandrium, lateral view; 15. Syntergosternite, anerior view; 16. Epandrium, posterior view; 17. Aedeagal complex, ventral view; 18. Aedeagal complex, lateral view.
Figure 11–14 in Two new species of Eurytoma (Hymenoptera: Eurytomidae), parasitoids of Bradybatus sp. (Coleoptera: Curculionidae) damaging seeds of Acer truncatum in China
Figure 11–14. Eurytoma truncatumi Yang, Liu & Cao, sp. nov., male. 11. Antenna. 12. Head and mesosoma in dorsal view. 13. Head in front view. 14. Mesosoma in lateral view.
Figures 7–14 in A taxonomic assessment and redefinition of the Lucanus fortunei species group in China (Coleoptera: Lucanidae: Lucaninae)
Figures 7–14. Habitus of Lucanus delavayi. 7. Male, dorsal view. 8. Male, ventral view. 9. Male, lateral view. 10. Major male. 11. Median male. 12. Minor male. 13. Female, dorsal view. 14. Female, ventral view. Scale bar = 10 mm.
Data supplementing Einhäuser, W., Neubert, C. R., Grimm, S., & Bendixen, A. (2024). High visual salience of alert signals can lead to a counterintuitive increase of reaction times. Scientific Reports, 14, 8858.
<p>These files supplement the publication <br>Einhäuser, W., Neubert, C. R., Grimm, S., & Bendixen, A. (2024). High visual salience of alert signals can lead to a counterintuitive increase of reaction times. <em>Scientific Reports, </em>14, 8858. https://doi.org/10.1038/s41598-024-58953-4</p> <p>The files data_expX.mat, where X is the experiment number (1-4), contain the data as described below. </p> <p>The files dataTraining_expX.mat contain the data of the first (training) block of each experiment. They are needed only for the supplemental material. </p> <p>To exemplify the usage, the functions figure2and3.m, figure4.m, figure5.m, figure6.m and Table1.m output the paper's figures and the data of Table 1, respectively; figureS2.m, figureS3.m, figureS4.m and figureS5.m output the figures of the supplemental material (figure S1 needs substantial amounts of external source code to compute the salience maps and is therefore not included).</p> <p><br>data_exp1.mat contains the following variables<br>For alert trials, variable of dimensions subjects x blocks x alert trials (20x10x64); note that only used participants and blocks with alert trials (2 through 11) are included in the data set:<br>alert_aud - the salience level of the alert tone (1-8, corresponding to 54dB(A) through 89 dB(A))<br>alert_vis - the salience level of the alert frame (1-8, corresponding to 0.10 to 8.50 Weber contrasts in logarithmic steps)<br>alert_side - the side on which the alert frame and the tone were presented (1-left, 2-right)<br>alert_fixOk - derived from eye movement data, was the first fixation closer to the alert square than to the center?<br>alert_primaryRT - primary-task reaction time (for alert trials)<br>alert_alertRT - alert-task reaction time <br>alert_correctAlert - was the response (up/down) to the alert correct?<br>alert_intrusionAlert - was there an intrusion (left/right pressed before up or down)?<br>alert_correctPrimary - was the primary task conducted correctly?<br>alert_intrusionPrimary - was there an intrusion for the primary task?<br>alert_timeToFixation - time to first fixation on alert square <br>alert_fixationToResp - time from beginning of fixation to response to the alert <br>alert_fixDur - duration of first fixation after trial onset</p> <p>For no-alert trials, variable of dimensions subjects x blocks x no-alert trials (20x10x448):<br>noalert_correctPrimary - was the primary task conducted correctly?<br>noalert_intrusionPrimary - was there an intrusion for the primary task? (i.e., up/down pressed before left/right)?</p> <p>For all trials, variable of dimensions subjects x blocks x no-alert trials (20x10x512):<br>all_correctPrimary - was the primary task conducted correctly?<br>all_intrusionPrimary - was there an intrusion for the primary task? (i.e., up/down pressed before left/right)?<br>all_RT - reaction time in the primary task<br>all_isAlertTrial - was the trial an alert trial? (useful to map no-alert trials and alert trials on all trials)</p> <p>In addition, there are some raw eye movement data for the alert blocks:<br>alert_eyeX, alert_eyeY - dimension 20 x 10 x 64 x 6000; x and y position in pixel coordinates relative to trial (and alert) onset, 1ms/sample, ends at conclusion of trials, filled up with NaN if duration was less than 6000ms <br>alert_eyeFixX, alert_eyeFixY, alert_eyeFixTon, alert_eyeFixDur - 20 x 10 x 64 x 15; x and y position, onset (in ms relative to trial onset) and duration of fixations during the trial (from onset to primary-task response), filled with NaN when less than 15 fixations were made. Note that the first entry of alert_eyeFixDur along the forth dimension will usually equal the alert_fixDur</p> <p><br>data_exp2.mat contains the same variables as data_exp1.mat with the following exceptions:<br>alert_vis - contains only two levels (1 and 2) corresponding to Weber contrasts of 0.10 and 2.39, respectively<br>alert_dur - the level of duration of the alert frame (1 through 8, corresponding to 25ms, 50ms, 100ms, 200ms, 300ms, 400ms, 600ms, 800ms)<br>alert_aud is not included (all tones were at 54 dB(A))<br>there are only 19 participants; hence the variables are of size 19 x ...<br>note: block 8 for subject 6 contains only 450 trials (57 alert trials), the remainder is filled with NaN.</p> <p><br>data_exp3.mat contains the same variables as data_exp1.mat with the following exceptions:<br>alert_aud - contains only two levels (1 and 2) corresponding to sound levels of 54 dB(A) and 79 dB(A) respectively<br>alert_dur - the level of duration of the alert tone (1 through 8, corresponding to 25ms, 50ms, 100ms, 200ms, 300ms, 400ms, 600ms, 800ms)<br>alert_vis is not included (all alert frames were at 0.10 contrast)</p> <p> </p> <p>data_exp4.mat contains the same variables as data_exp1.mat with the following exceptions:<br>alert_aud - contains only two levels (1 and 2) corresponding to sound levels of 54 dB(A) and 79 dB(A) respectively<br>alert_vis is not included and replaced by<br>alert_condBefore - alert frame contrast level before the saccade (1 - 0.10 contrast, 2 - 2.39 contrast)<br>alert_condAfter - alert frame contrast level after the saccade (1 - 0.10 contrast, 2 - 2.39 contrast)</p> <p><br>dataTraining_expX.mat contains for the first (training) block of experiment X (X being 1, 2, 3 or 4) the following variables of size 20x512 (participant x trial) [19x512 in case of Experiment 2]:<br>all_correctPrimary - was the primary task conducted correctly?<br>all_RT - reaction time in the primary task<br>[Note that there are no alert trials in this block and these data are only used in the supplementary material (part 4)]</p>
Figuras 14-25 in Reevaluación del género Andonectes Guéorguiev, 1971 y establecimiento de nuevas combinaciones para el género Platynectes (Agametrus) Régimbart, 1879 (Coleoptera: Dytiscidae: Agabinae) en Venezuela
Figuras 14-25. Escleritos genitales de las especies de Platynectes (Agametrus) de Venezuela. 14. P. (A.) apure. 15. P. (A.) bordoni. 16. P. (A.) gregarius. 17. P. (A.) intermedius. 18. P. (A.) meridensis. 19. P. (A.) mildredae. 20. P. (A.) milla. 21. P. (A.) pineiroi. 22. P. (A.) septentrionalis. 23. P. (A.) similaris. 24. P. (A.) trujillo. 25. P. (A.) venezuelanus. lbm = lóbulo medio, pde = parámero izquierdo excepto en P. (A.) pineiroi (parámero izquierdo), lto = lateroterguito, gcxto = gonocoxa, gcxto = gonocoxito. / 14. P. (A.) apure. 15. P. (A.) bordoni. 16. P. (A.) gregarius. 17. P. (A.) intermedius. 18. P. (A.) meridensis. 19. P. (A.) mildredae. 20. P. (A.) milla. 21. P. (A.) pineiroi. 22. P. (A.) septentrionalis. 23. P. (A.) similaris. 24. P. (A.) trujillo. 25. P. (A.) venezuelanus. lbm = middle lobe, pde = left paramere except in P. (A.) pineiroi (left paramere), lto = lateroterguite, gcxto = gonocoxa, gcxto = gonocoxite.
Figure 14 in Population ecology of Ctenolepisma (C.) udumalpetense (Insecta: Zygentoma: Lepismatidae) in a deciduous forest floor of the Trimurti Dam, Tamil Nadu, India
Figure 14. Showing the monthly fluctuations of male, female and nymph population, temperature and humidity in Row III.
Figures 13-18. Chrysodeixis chalcites Esper 13. Forewing, 14. Hindwing, 15 in Status of Chrysodeixis chalcites Esper and Chrysodeixis eriosoma (Doubleday) of family Noctuidae (Lepidoptera) in India as determined by DNA barcoding and morphological characterization
Figures 13-18. Chrysodeixis chalcites Esper 13. Forewing, 14. Hindwing, 15. Eight photos of forewing spots; Chrysodeixis acuta (Walker) – 16. Forewing, 17. Hindwing, 18. Eight photos of forewing spots.
Figure 14 in The diversity of Triassic South American sphenodontians: a new basal form, clevosaurs, and a revision of rhynchocephalian phylogeny
Figure 14. Reconstructions of the skulls of Clevosaurus brasiliensis (A–D) and Microsphenodon bonapartei gen. et sp. nov. (E–H). A, B, cranium of C. brasiliensis in: A, dorsal; B, ventral views. C, right lateral view of the cranium and mandible of C. brasiliensis. D, a medial view of the right mandible of C. brasiliensis. E, F, cranium of M. bonapartei in: E, dorsal, F, ventral views. G, a right lateral view of the cranium and mandible of M. bonapartei. H, a medial view of the right mandible of M. bonapartei. Abbreviations: ang, angular; art, articular; bo, basioccipital; bs, basisphenoid; cor, coronoid; d, dentary; epi, epipterygoid; ept, ectopterygoid; f, frontal; j, jugal; m, maxilla; n, nasal; p, parietal; pal, palatine; pm, premaxilla; po, postorbital; pof, postfrontal; pfr, prefrontal; pra, prearticular; ps, parasphenoid; pt, pterygoid; q, quadrate; so, supraoccipital; sq, squamosal; st, supratemporal; sur, surangular; vo, vomer. Scale bars equal 10 mm.
FIGURE 14 in Miocene and Pliocene amphibians from Hambach (Germany): New evidence for a late Neogene refuge in northwestern Europe
FIGURE 14. Axial elements of Latonia sp. from Hambach: atlas (IPB-HaH 2071) in anterior (A), dorsal (B), left lateral (C), ventral (D) and posterior (E) views; trunk vertebra (IPB-HaH 2073) in anterior (F), dorsal (G) and posterior (H) views; trunk vertebra (IPB-HaR 2032) in anterior (I), dorsal (J) and left lateral (K) views; sacral vertebra (IPB-HaH 2219) in dorsal view (L); sacral vertebra (IPB-HaR 2014) in dorsal (M), anterior (N) and ventral (O) views; urostyle (IPB-2199) in dorsal view (P); urostyle (IPB-HaH 2200) in dorsal view (Q); urostyle (IPB-HaR 2034) in dorsal view (R). Scale bars equal 1 mm. Abbreviations: f, fissure; k, keel.
FIGURE 14 in Comparison of Miocene to early Pleistocene-aged Castor californicus (Rodentia: Castoridae) to extant beavers and implications for the evolution of Castor in North America
FIGURE 14. Variation line graph calculated by coefficients of variation with sample size correction for Castor canadensis and C. californicus postcranial measurements. Note that C. fiber is excluded due to limited sampling. Castor canadensis and C. californicus both contains high levels of variation in postcranial elements. See Table 17 for descriptive statistics, coefficients of variation, and ANOVA results.
FIGURE 14 in Fossil snakes of the Penny Creek Local Fauna from Webster County, Nebraska, USA, and the first record of snakes from the Early Clarendonian (12.5-12 Ma) of North America
FIGURE 14. Complete-linkage hierarchical cluster analysis showing the relative similarity of snake assemblages from 19 Barstovian-Blancan localities in Nebraska based on presence-absence.. Three major clusters are visible. From the left, the first cluster contains only Bw 123, the unique Pratt Slide local fauna; the second cluster contains all Barstovian and Clarendonian faunas minus Bw 123, but with the addition of Hemphillian Cn 106b (Thamnophis + Colubrinae indet.); and the third cluster, containing all Hemphillian through Blancan sites except Cn 106b.
FIGURE 14 in A vanished ecosystem: Sophora microphylla (Kōwhai) dominated forest recorded in mid-late Holocene rock shelters in Central Otago, New Zealand
FIGURE 14. Muehlenbeckia sp. A. Abaxial surface with stomatal complexes below and peltate trichome with divided base above (LX2891, Shelter-95, scale bar equals 40 μm). B. Three stomatal complexes among fine surface ridging and peltate trichome with divided base at lower left (LX3100, Coprolite-36, scale bar equals 40 μm).
FIGURE 14. 1-4 in Taxonomic notes on Recent Foraminifera from the Continental Shelf-Slope Region of Southwestern Bay of Bengal, East Coast of India
FIGURE 14. 1-4, Globigerinoides sacculifera (Brady, 1877) in dorsal view (scale equals 500 μm) (1); in ventral view (scale equals 400 μm) (2); in dorsal view (scale equals 500 μm) (3); and in ventral view (scale equals 500 μm) (4). 5-6, Globigerinoides triloba (Reuss, 1850) in dorsal view (scale equals 400 μm) (5) and in ventral view (scale equals 400 μm) (6). 7-8, Globoturborotalita sp. in dorsal view (scale equals 100 μm) (7) and in ventral view (scale equals 100 μm) (8). 9-10, Sphaeroidinella dehiscens (Parker and Jones, 1865) in dorsal view (scale equals 400 μm) (9) and in ventral view (scale equals 400 μm) (10). 11, Candeina nitida d'Orbigny, 1839 in dorsal view (scale equals 100 μm). 12, Globigerinita glutinata (Egger, 1893) in dorsal view (scale equals 100 μm). 13-14, Globorotalia cultrata (d'Orbigny, 1839) in dorsal view (scale equals 100 μm) (13) and in ventral view (scale equals 100 μm) (14). 15-16, Globorotalia menardii (d'Orbigny, 1826) in dorsal view (scale equals 400 μm) (15) and in ventral view (scale equals 500 μm) (16). 17-18, Globorotalia tumida (Brady, 1877) in dorsal view (scale equals 500 μm) (17) and in ventral view (scale equals 500 μm) (18). 19-20, Globorotalia ungulata Bermúdez, 1961 in dorsal view (scale equals 300 μm) (19) and in ventral view (scale equals 200 μm) (20).
FIGURE 14. 1–8 in Synoptic revision of the Silurian fauna from the Pentland Hills, Scotland described by Lamont (1978)
FIGURE 14. 1–8: Plumulites ruskini Lamont, 1978, from locality R82, Wether Law Linn Formation; 1, 2: specimen NMS G. 1979.77.17 (part and counterpart), figured by Lamont on plate XXVIII, figure 13; 3: specimen NMS G.1979.77.18, figured by Lamont on plate XXVIII, figure 14; 4: specimen NMS G.1979.77.19, figured by Lamont on plate XXVIII, figure 15; 5: handwritten label; 6: specimen NMS G.1979.77.20, figured by Lamont on plate XXVIII, figure 16; 7: specimen NMS G.1979.77.21, figured by Lamont on plate XXVIII, figure 17; 8: specimen NMS G.1979.77.22, not figured by Lamont. All specimens from the Lamont Collection, possibly re-registered from NMS G.1876.42.8 (Henderson Collection). Scale bars: 1 mm (figures 1–4, 6–8).
Figure 14 in On a remarkable new species of Tharsis, a Late Jurassic teleostean fish from southern Germany: its morphology and phylogenetic relationships
Figure 14. Caudal vertebrae and caudal skeleton of Tharsis dubius (JME-SOS 02633) in lateral view. Note the polyural condition of ural centra U1 to U6. Arrows point to the dorsal processes of caudal fin rays. Note that the dorsal processes have additional elongate processes. Abbreviations are as follows: an.p, anterior process; d.scu, piece of dorsal scute; E1–3, epural 1–3; H1–3, hypurals 1–3; nsPU2, 1, neural spine of preural centrum 2, 1; PH, parhypural; PU4, 1, preural centrum 4, 1; UN1, 5, uroneural 1, 5.
Figure 14 in A morphometric approach to conch ontogeny of Cymaclymenia and related genera (Ammonoidea, Late Devonian)
Figure 14. Cross sections (A–I; all × 1.5) and ontogenetic trajectories (J–M) of Cymaclymenia subvexa n. sp. from the Anti-Atlas of Morocco. (A) Paratype MB.C.22647.1 (Korn 2009 Coll.) from Madène el Mrakib. (B) Paratype MB.C.22686.1 (Wendt Coll.) from Khorb et Attil. (C) Paratype MB.C.22675 (Wendt Coll.) from Bou Ifarherioun. (D) Paratype MB.C.22636.2 (Korn 1998 Coll.) from Madène el Mrakib. (E) Paratype MB.C.22682 (Wendt Coll.) from Taourirt. (F) Paratype MB.C.22686.2 (Wendt Coll.) from Khorb et Attil. (G) Paratype MB.C.22683.1 (Wendt Coll.) from Taourirt. (H) Paratype MB.C.22684.1 (Wendt Coll.) from Taourirt. (I) Paratype MB.C.22636.3 (Korn 1998 Coll.) from Madène el Mrakib. (J) Conch width index (ww / dm). (K) Umbilical width index (ww / wh). (L) Whorl width index (uw / dm). (M) Whorl expansion rate (WER).
Fig. 14 in A new cryptic species of Polybiidae (Crustacea: Decapoda: Portunoidea) from the East Atlantic, with considerations on the genus Polybius
Fig. 14. Polybius holsatus (Fabricius, 1798), ♂ from Belgium, Duinbergen (RBINS, INV. 187221). A. Dorsal habitus. B. Facial habitus. C. Ventral habitus. D. Carpus of right pereiopod.
F I G U R E 1 Map displaying the 14 in Migration patterns and navigation cues of Atlantic salmon post-smolts migrating from 12 rivers through the coastal zones around the Irish Sea
F I G U R E 1 Map displaying the 14 capture sites in 12 rivers where Atlantic salmon smolts (n = 1008) were captured for tagging in England, Scotland, Northern Ireland and the Republic of Ireland for this study. In addition, 60 hatchery origin smolts were tagged and released in the River Burrishoole. The coastal region each river belongs to is referenced in brackets next to the river name. Where Region one (1) refers to the Solway Firth (Rivers Derwent, Nith, Bladnoch); Region two (2) refers to the Clyde Estuary (Rivers Endrick and Gryffe); Region three (3) refers to the Bush Coastal region (rivers Bann, Bush, Carey and Glendun); Region four (4), refers to Lough Foyle (rivers Roe and Faughan); Region five (5), refers to Clew Bay (River Burrishoole). Tagged fish release sites are represented by stars, and acoustic receivers (n = 183) are represented by gray dots. Marine monitoring lines (A and B) in the Irish Sea are labeled in alphabetical order from south to north. Twenty-two acoustic receivers were initially deployed at monitoring line A. One hundred and eight acoustic receivers were deployed at monitoring line B and are labeled in numerical order from the furthest west receiver (R1) on the monitoring line to the furthest east (R108). Refer to Figure S2 for the locations of acoustic receivers that were not retrieved from marine monitoring line A (n = 2) and B (n = 9).
Fig. 14 in A late Paleocene fauna from shallow-water chemosynthesis-based ecosystems, Spitsbergen, Svalbard
Fig. 14. Arcticid bivalve?Arctica sp. from the upper Paleocene, Basilika Formation, Fossildalen, Spitsbergen, Svalbard. NRM-PZ Mo 149143, shell, left (A1) and right (A2) valves, dorsal (A3) and anterodorsal (A4) views, oblique dorsal view of left valve showing very fine commarginal ornament (A5).
Fig. 14 in A new assessment of the Late Devonian antiarchan fish Bothriolepis leptocheira from South Timan (Russia) and the biotic crisis near the Frasnian-Famennian boundary
Fig. 14. Antiarchan fish Bothriolepis leptocheira jeremejevi (Rohon, 1900), reconstruction of the head, the trunk armour and the pectoral fins in ventral view, based on IG KSC 155/10-1, IG KSC 155/10-2, and IG KSC 155/10- 3. Abbreviations: AVL, anterior ventro-lateral plate; Cv1–4, ventral central plate 1 to 4; Ifg, inferognathal plate; La, lateral plate; Ml2–5, lateral marginal plates 2 to 5; Mm4, mesial marginal plate 4; MV, median ventral plate; Prl, prelateral plate; Prm, premedian plate; PVL, posterior ventro-lateral plate; SM, semilunar plate; SMg, submarginal plate; T, terminal plate.
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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.