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Figure 12 from: Rodríguez-Flores PC, Gutiérrez-Rodríguez J, Aguirre-Ruiz EF, García-París M (2016) Salt lakes of La Mancha (Central Spain): A hot spot for tiger beetle (Carabidae, Cicindelinae) species diversity. ZooKeys 561: 63-103. https://doi.org/10.3897/zookeys.561.6042
Figure 12 - Behavioural observations on Cephalota dulcinea A Specimen of Cephalota dulcinea located in a trail devouring a winged hymenopteran. Note the number of insect remains located behind the specimen (ants, other Hymenoptera and Coleoptera), suggesting that the spot is used as a hunting post B A couple of Cephalota dulcinea involved in courship C A recently killed specimen of Cephalota dulcinea in a trail, about to be seized by ants D Trail located near laguna de Pajares with a large colony of Cephalota dulcinea, Cephalota maura maura and scattered Cylindera paludosa. We hypothesize that these trails, despite of being surrounded by unfavourable habitat, might be used as dispersal corridors between lakes, facilitating the maintenance of metapopulation systems. Photographs by MG-P.
Figure 3 from: Rodríguez-Flores PC, Gutiérrez-Rodríguez J, Aguirre-Ruiz EF, García-París M (2016) Salt lakes of La Mancha (Central Spain): A hot spot for tiger beetle (Carabidae, Cicindelinae) species diversity. ZooKeys 561: 63-103. https://doi.org/10.3897/zookeys.561.6042
Figure 3 - Representative specimens of Cephalota from La Mancha wetlands. A Cephalota (Taenidia) dulcinea (Sánchez Gómez, Cuenca) B Cephalota (Cassolaia) maura (Arroyo San Marcos, Ciudad Real) C Cephalota (Taenidia) circumdata imperialis (Tirez, Toledo). Photographs by MG-P.
Figure 7 from: Rodríguez-Flores PC, Gutiérrez-Rodríguez J, Aguirre-Ruiz EF, García-París M (2016) Salt lakes of La Mancha (Central Spain): A hot spot for tiger beetle (Carabidae, Cicindelinae) species diversity. ZooKeys 561: 63-103. https://doi.org/10.3897/zookeys.561.6042
Figure 7 - Observations of Calomera littoralis littoralis at Laguna de Manjavacas (left) and La Dehesilla (upper right). Colours indicate the month in which observations were made (see legend). Note seasonal changes in specimen's location as the water front retreats or following changes in humidity of the soil. Blue squares correspond to the habitat shown in Fig. 6b.
Figure 2 from: Rodríguez-Flores PC, Gutiérrez-Rodríguez J, Aguirre-Ruiz EF, García-París M (2016) Salt lakes of La Mancha (Central Spain): A hot spot for tiger beetle (Carabidae, Cicindelinae) species diversity. ZooKeys 561: 63-103. https://doi.org/10.3897/zookeys.561.6042
Figure 2 - Representative specimens of tiger beetles from La Mancha wetlands A Calomera littoralis littoralis (La Dehesilla, Cuenca) B Cicindela campestris campestris (La Dehesilla, Cuenca) C Cicindela maroccana (La Sal, Toledo) D Cylindera paludosa (El Longar, Toledo) E Lophyra flexuosa flexuosa (El Pardo, Madrid) F Myriochila melancholica melancholica (Tirez, Toledo). Photographs by MG-P.
Figure 10 from: Rodríguez-Flores PC, Gutiérrez-Rodríguez J, Aguirre-Ruiz EF, García-París M (2016) Salt lakes of La Mancha (Central Spain): A hot spot for tiger beetle (Carabidae, Cicindelinae) species diversity. ZooKeys 561: 63-103. https://doi.org/10.3897/zookeys.561.6042
Figure 10 - Behavioural observations on Cephalota circumdata imperialis. A, B A few specimens of Cephalota circumdata located at the shade of a rock in the middle of the exposed salt flat C Individual photographed on the wet mud under the remains of a plastic bag, also in the salt flat. This behaviour is atypical for the species, which is generally active at full sunlight in mid summer in the area. The observations were made the 13th of June, at mid-day, the first date in which activity of the species was recorded. It is possibly that the specimens had just eclosed and wait in the shade while hardening their integument. Photographs by MG-P.
Figure 1 from: Tan M, Armbruster JW (2016) Two new species of spotted Hypancistrus from the Rio Negro drainage (Loricariidae, Hypostominae). ZooKeys 552: 123-135. https://doi.org/10.3897/zookeys.552.5956
Figure 1 - Hypancistrus phantasma sp. n., holotype, 123.3 mm SL, dorsal, lateral, and ventral views, MZUSP 116531, Rio Uaupes. Photographs by M Tan.
Figure 3 from: Tan M, Armbruster JW (2016) Two new species of spotted Hypancistrus from the Rio Negro drainage (Loricariidae, Hypostominae). ZooKeys 552: 123-135. https://doi.org/10.3897/zookeys.552.5956
Figure 3 - Hypancistrus margaritatus sp. n., holotype, 45.6 mm SL, dorsal, lateral, and ventral views, AUM 35610, Takutu River. Photographs by M Tan.
Figure 4 from: Tan M, Armbruster JW (2016) Two new species of spotted Hypancistrus from the Rio Negro drainage (Loricariidae, Hypostominae). ZooKeys 552: 123-135. https://doi.org/10.3897/zookeys.552.5956
Figure 4 - Photograph of live Hypancistrus margaritatus holotype, AUM 35610, Takutu River. Image flipped horizontally. Photograph by MH Sabaj Pérez.
Figure 2 from: Tan M, Armbruster JW (2016) Two new species of spotted Hypancistrus from the Rio Negro drainage (Loricariidae, Hypostominae). ZooKeys 552: 123-135. https://doi.org/10.3897/zookeys.552.5956
Figure 2 - Map of South America, with known localities for Hypancistrus phantasma sp. n. (●) and Hypancistrus margaritatus sp. n. (■).
Figure 2 from: Colombo Ferreguetti Á, Pereira BC, Bergallo HG (2018) Assessing the population density of the spotted paca, Cuniculus paca, (Rodentia: Cuniculidae) on an Atlantic Forest island, southeastern Brazil. Zoologia 35: 1-5. https://doi.org/10.3897/zoologia.35.e23133
Figure 2 Plot of the detection function for spotted pacas based on the AIC selected Conventional Distance Sampling (CDS) model. Histogram represents the probability of detection for each distance interval. The curved line is the detection function, showing the probability that a spotted paca is observed as a function of distance from the transect line.
Figure 1 from: Colombo Ferreguetti Á, Pereira BC, Bergallo HG (2018) Assessing the population density of the spotted paca, Cuniculus paca, (Rodentia: Cuniculidae) on an Atlantic Forest island, southeastern Brazil. Zoologia 35: 1-5. https://doi.org/10.3897/zoologia.35.e23133
Figure 1 Ilha Grande in the state of Rio de Janeiro, Brazil and location of the transects. Black triangle representing the Abraão village.
Spotted turtle dispersal microsatellite DNA sex and site data
<p>Sex-biased dispersal is common in many animals, with male-biased dispersal often found in studies of mammals and reptiles, including interpretations of spatial genetic structure, ostensibly as a result of male-male competition and a lack of male parental care. Few studies of sex-biased dispersal have been conducted in turtles, but a handful of studies, in saltwater turtles and in terrestrial turtles, have detected male-biased dispersal as expected. We tested for sex-biased dispersal in the endangered freshwater turtle, the spotted turtle (<em>Clemmys</em> <em>guttata</em>) by investigating fine-scale genetic spatial structure of males and females. We found significant spatial genetic structure in both sexes, but the patterns mimicked each other. Both males and females typically had higher than expected relatedness at distances < 25 km, and in many distance classes greater than 25 km, less than expected relatedness. Similar patterns were apparent whether we used only loci in Hardy-Weinberg equilibrium (n = 7) or also included loci with potential null alleles (n = 5). We conclude that, contrary to expectations, sex-biased dispersal is not occurring in this species, possibly related to the reverse sexual dimorphism in this species, with females having brighter colors. We did, however, detect significant spatial genetic structure in males and females, separate and combined, showing philopatry within a genetic patch size of < 25 km in <em>C</em>. <em>guttata</em>, which is concerning for an endangered species whose populations are often separated by distances greater than the genetic patch size.</p>
Raw results of nanoLC-Q-TOF-MS /MS for four immunoblotting spots with elevated autoantibody levels in early ESCC.
<p>NanoLC-Q-TOF-MS/MS was used to identified the candidate autoantibodies which were detected from the serum of ESCC patients but not from healthy controls. Mascot searching engine were used to make a confirmation of the information provided by MS spectrum. In the database are the original results of the immunoblotting spots that we screened.</p>
Fig. 20 in Between areolated and band-shaped spots: a revision of Lacronia Strand, 1942 (Opiliones, Gonyleptidae)
Fig. 20. Lacronia tenuis (Roewer, 1917) comb. nov., ♂ (MNRJ 5533ꜝ), penis, distal part. A. Dorsal view. B. Left lateral view. C. Ventral view. D. Detail of stylus and ventral process, dorso-lateral view. Scale bars: A–C = 100 μm; D = 20 μm.
Fig. 4 in Between areolated and band-shaped spots: a revision of Lacronia Strand, 1942 (Opiliones, Gonyleptidae)
Fig. 4. Lacronia spp., schematic illustrations of the ♂ DS, showing the background variation and tubercles patterns of the specimens in vivo (except for L. boraceae (B. Soares, 1942) comb. nov., which information was only available in alcohol). A. L. ceci Kury & Orrico, 2006. B. L. camboriu Kury, 2003. C. L. ricardoi Kury, 2003. D. L. serripes (Mello-Leitão, 1923). E. L. boraceae comb. nov. F. L. nigra (B. Soares, 1942) comb. nov. G. L. tenuis (Roewer, 1917) comb. nov. Scale bars = 1 mm.
Fig. 1 in Between areolated and band-shaped spots: a revision of Lacronia Strand, 1942 (Opiliones, Gonyleptidae)
Fig. 1. The most frequent tree (k-values = 3, 4, 5, 6, 10, 15 and 20) retrieved using the Mendes (2011) protocol. Clade support values are indicated above the branches (Bremer index / SFq values). Clade stability is indicated below the branches by the sensitivity plots ('Navajo rugs'), which denotes the tested k-values (black squares indicate monophyly; white squares indicate non-monophyly). The k-values (= 2 and 3) retrieved two different trees, represented here as 2.1, 2.2, 3.1 and 3.2. in the Navajo rugs. Colored backgrounds indicate the following groups: Discocyrtus Holmberg, 1878 s. str. (grey), Lacronia Strand, 1942 (salmon), Mitobatinae Simon, 1879 (green), Neopachylinae Carvalho & Kury, 2020 (yellow), Pachylinae Sørensen, 1884 s. str. (purple) and Roeweriinae Carvalho & Kury, 2018 (blue). A red circle marks the DRMN-group. The unmarked groups are not members of either DRMN or Pachylinae s. str.
Wayfinding artificial intelligence to detect clinically meaningful spots of retinal diseases: Artificial intelligence to help retina specialists in real world practice
<p>Dataset related to the Ambiguity index of 300 images analyzed in the thesis.</p>
FIG. 2 in A Successful Reintroduction of Columbia Spotted Frog (Rana luteiventris) through Repatriation of Recently Hatched Larvae
FIG. 2. Total CSF egg mass counts and cumulative depositional areas at Taylors Fork.
Fig. 4 in Argyrotoxins A-C, a trisubstituted dihydroisobenzofuranone, a tetrasubstituted 2-hydroxyethylbenzamide and a tetrasubstitutedphenyl trisubstitutedbutyl ether produced by Alternaria argyroxiphii, the causal agent of leaf spot on African mahogany trees (Khaya senegalensis)
Fig. 4. Synthesis of biphenylamide 1a from argyrotoxin A (1).
Spot-Check Noninvasive Hemoglobin (SpHb) Clinical Validation of INVSENSOR00026
ClinicalTrials.gov study NCT03610269. IPD Sharing: NO. Countries: 1. Publications: 0.
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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.