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Figs. 16–17 in Larval Morphology Of Agabetes Crotch (Coleoptera: Adephaga: Dytiscidae): The Hypothesis Of Sister-Group Relationship With The Subfamily Laccophilinae Revisited
Figs. 16–17. Agabetes acuductus (Harris) Instar III, metathoracic legs (excluding tarsus). 12) Anterior face; 13) posterior face. Sensillar series: A = anterior; D = dorsal; Pr = proximal. Scale bar = 0.10 mm.
Fig. 6 in The hypothesis of adaptive radiation in evolutionary biology: hard facts about a hazy concept
Fig. 6 Frequency at which the different regions of the world were investigated. The number of occurrences for each area between 2003 and 2012 corresponds to the number of case studies (potentially several case studies per article) where a taxon has likely radiated in this given area (see Table 1). Mainland: light brown ≤50 and dark brown>50. Oceans: light green = [1–5] and dark green =]5–20]. Islands s.l. (ellipses): light blue (light gray in the printed version) = [1–5], dark blue (dark gray) =]5–25], and purple (medium gray)>25
Fig. 4 in The hypothesis of adaptive radiation in evolutionary biology: hard facts about a hazy concept
Fig. 4 Sampling ratio of the group having possibly radiated for the three most frequently studied taxa. NA case studies for which the sampling ratio was not specified in the article or could not be retrieved easily. Percentages are relative to case studies (potentially several case studies per article) between 2003 and 2012. Color boxes follow the clockwise succession of categories in the pie chart
Audiovisual multisensory Kappa and reverse Kappa effect: Cognitive resource hypothesis
Open the record for dataset details and reuse information.
FIGURES 44–51. 44, K in Description of Khamul, gen. n. (Hymenoptera: Chalcidoidea: Eurytomidae), with a hypothesis of its phylogenetic placement
FIGURES 44–51. 44, K. erwini, dorsal head; 45, K. erwini, apex clava; 46, K. erwini, propodeum; 47, K. erwini, lateral procoxa; 48, K. erwini, digitiform ornamentation of postgenal bridge; 49, K. erwini, lateral petiole; 50, K. erwini, male antenna; 51, K. erwini, male antenna, pedicel to F4. Note: all females unless otherwise noted.
Figure 4 in On Liljeborgia fissicornis (M. Sars, 1858) and three related new species from Scandinavia, with a hypothesis on the origin of the group fissicornis
Figure 4. Liljeborgia caliginis sp. nov., female, holotype, Svalbard, R/V Jan Mayen sta. 807–97, TSZCr 10408. (A) Left P3; (B) articles 5–7 of left P3; (C) left P4; (D) articles 5–7 of left P4.
Figures 128–135 in Phylogeny of Neotropical Castniinae (Lepidoptera: Cossoidea: Castniidae): testing the hypothesis of the mimics as a monophyletic group and implications for the arrangement of the genera
Figures 128–135. Female genitalia and associated characters, dorsal view: 128, Synpalamides amycus (Cramer [1779]) comb. nov.; 129, Yagra fonscolombe (Godart, [1824]); 130, Athis inca (Walker, 1854); 131, Athis palatinus (Cramer, 1777); 132, Telchin syphax (Fabricius, 1775); 133, Imara therapon (Kollar, 1839) comb. nov.; 134, Synpalamides fabricii (Swainson, 1823) comb. nov.; 135, Castnia invaria Walker, 1854. Scale bar: 1 mm.
Figures 111–116 in Phylogeny of Neotropical Castniinae (Lepidoptera: Cossoidea: Castniidae): testing the hypothesis of the mimics as a monophyletic group and implications for the arrangement of the genera
Figures 111–116. Female genitalia and associated characters, dorsal view: 111, Imara acraeoides (Guérin-Ménéville, [1832]) comb. nov.; 112, Synpalamides amycus (Cramer [1779]) comb. nov.; 113, Castnius marcus (Jordan, 1908); 114, Castnia invaria Walker, 1854; 115, Prometheus cochrus (Fabricius, 1787); 116, Ceretes marcelserres (Godart, [1824]). Scale bars: 1 mm.
Figures 49–51 in Phylogeny of Neotropical Castniinae (Lepidoptera: Cossoidea: Castniidae): testing the hypothesis of the mimics as a monophyletic group and implications for the arrangement of the genera
Figures 49–51. Wing scales: 49, piliform scales on the hindwing base of Imara pallasia (Eschscholtz, 1821); 50, oblong scales on the hindwing of Yagra fonscolombe (Godart, [1824]); 51, projection on the inner margin of the forewing with oblong scales of Synpalamides amycus (Cramer [1779]) comb. nov. Scale bars: 1 cm.
Figures 87–95 in Phylogeny of Neotropical Castniinae (Lepidoptera: Cossoidea: Castniidae): testing the hypothesis of the mimics as a monophyletic group and implications for the arrangement of the genera
Figures 87–95. Tegumen, uncus, and associated characters, dorsal view: 87, Yagra dalmannii (Gray, 1838); 88, Synpalamides ctesiphon (Hübner, [1820]) comb. nov.; 89, Prometheus heliconioides (Herrich-Schäffer, [1853]) comb. nov.; 90, Telchin atymnius (Dalman, 1824); 91, Castnia invaria Walker, 1854; 92, Imara satrapes (Kollar, 1839); 93, Telchin evalthe (Fabricius, 1775) comb. nov.; 94, Castnius pelasgus (Cramer, [1779]); 95, Synpalamides hegemon (Kollar, 1839) comb. nov. Scale bars: 1 mm.
Figure 2. BEAST chronogram from a in Molecular data extend Australian Cricotopus midge (Chironomidae) species diversity, and provide a phylogenetic hypothesis for biogeography and freshwater monitoring
Figure 2. BEAST chronogram from a data set of single representatives per species/clade that corresponds with Table 1. Lettered nodes are those for which time to most recent common ancestor (tmrca) was estimated and correspond with Table 1; black stars indicate nodes to which prior calibrations were applied. The time scale is in millions of years before present.
Figure 9 in An extraordinary new genus of spiders from Western Australia with an expanded hypothesis on the phylogeny of Tetragnathidae (Araneae)
Figure 9. Pinkfloydia harveii sp. nov. Male (holotype): A, lateral; B, frontal; C, dorsal; D, ventral. Cephalothorax length is 1.36 mm (see species description for measurements).
Figure 1 in Taxonomic, palaeobiological and evolutionary implications of a phylogenetic hypothesis for Ornithischia (Archosauria: Dinosauria)
Figure 1. Hypotheses of the phylogenetic relationships of dinosaurs compared: A, the traditional ('Seeley') hypothesis (e.g. Nesbitt 2011; Langer et al., 2017) incorporating the clade Silesauridae. B, the 'Phytodinosauria' hypothesis (e.g. Paul 1984; Bakker, 1986). C, the 'Ornithoscelida' hypothesis (e.g. Baron et al., 2017a, 2017b; Cau, 2018). D, the 'Seeley' hypothesis with Silesauridae placed as the sister-taxon to traditional ornithischians (e.g. Langer & Ferigolo, 2013; Cabreira et al., 2016). E, paraphyletic silesaurs as stem-lineage ornithischians (Müller & Garcia, 2020a). Silhouettes are based on artwork by Márcio L. Castro.
Fig. A2 in Auditory system biophysics in a new species of false-leaf katydid (Tettigoniidae: Pseudophyllinae) supports a hypothesis of broadband ultrasound reception
Fig. A2. Calling song of Eubliastes chlorodictyon from Montealegre-Z and Morris (1999). Caption: 'Ecuador specimen: A, Single call. Colombian specimen: B, Single call. C, Power spectrum. D, Portion of a pulse at high resolution showing sinusoid waveform. E, Waterfall spectral display of one call.
Fig. 4 in Auditory system biophysics in a new species of false-leaf katydid (Tettigoniidae: Pseudophyllinae) supports a hypothesis of broadband ultrasound reception
Fig. 4. Eubliastes viridicorpus sp. nov. female tracheae resonances. A, female acoustic tracheae; B, right trachea anatomy showing model boundary conditions; C, left trachea first eigenfrequency; D, right trachea first eigenfrequency; E, left trachea second eigenfrequency; F, right trachea second eigenfrequency; G, left trachea third eigenfrequency; H, right trachea third eigenfrequency; I, left trachea fourth eigenfrequency; J, right trachea fourth eigenfrequency.
Fig. 3 in Auditory system biophysics in a new species of false-leaf katydid (Tettigoniidae: Pseudophyllinae) supports a hypothesis of broadband ultrasound reception
Fig. 3. Eubliastes viridicorpus sp. nov. auditory system. A. male auditory system: (left to right) acoustic spiracle, acoustic trachea, auditory pinnae; B. female auditory system (left to right same as A); C. female auditory pinnae resonances; D. male auditory pinnae resonances; E, auditory pinnae resonances across other species of the genus Eubliastes. Abbreviations: Lapc, Left anterior pinna cavity; Rapc, Right anterior pinna cavity; Lppc, Left posterior pinna cavity; Rppc, Right posterior pinna cavity.
Fig. A3 in Auditory system biophysics in a new species of false-leaf katydid (Tettigoniidae: Pseudophyllinae) supports a hypothesis of broadband ultrasound reception
Fig. A3. Calling song of Eubliastes pollonerae from ter Hofstede et al. (2020). Caption: 'Photographs and calling song spectrograms of Eubliastes pollonerae. A. Male (photo credit: H. ter Hofstede); B. Female (photo credit: C. Kernan); C. and D. Spectrogram (top panel) and oscillogram (bottom panel) of one call at different time scales'.
Study Confirms or Refutes the Hypothesis That the Autologous Bone Marrow Concentrate Together With the Allograft is a Better Alternative for the Posterolateral Fusion in Spine Surgery Than the Allogra
ClinicalTrials.gov study NCT01603836. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Amoeba Predation of Cryptococcus: A Quantitative and Population Genomic Evaluation of the Accidental Pathogen Hypothesis
GEO Series GSE238170. Cryptococcus neoformans. 32 samples. Type: Expression profiling by high throughput sequencing.
Exploring the social brain hypothesis in spiders
<p>Supplementary material</p>
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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.