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3,015 results for “occurrences”
Figure 2 in Dragonflies and damselflies (Odonata) from Flores Island, Lesser Sunda Archipelago: New occurrences in extreme environments and an island-level checklist of this group
Figure 2. Examples of extreme habitats on Flores and Kanawa islands (Lesser Sunda Archipelago, Indonesia). (A) Sano Ngoang Lake on Flores Island. This highly acidic, slightly brackish lake supports viable populations of Orthetrum sabina, Agriocnemis pygmaea, and Xiphiagrion cyanomelas. (Photo: Wiwin Windari Petersen). (B) Coastal marsh near Labuan Bajo on Flores Island. Habitat of Diplacodes trivialis, Neurothemis intermedia excelsa, N. terminata, Pantala flavescens, and Rhyothemis phyllis ixias. (Photo: Yulia S. Kolosova). (C) Dry grass savanna with Indian jujube (Ziziphus mauritiana) and tamarind (Tamarindus indica) near the foothill on Kanawa Island (waterless during dry season). Site of Pantala flavescens occurrence (vagrant specimen). (Photo: Yulia S. Kolosova).
Figure 6 in Dragonflies and damselflies (Odonata) from Flores Island, Lesser Sunda Archipelago: New occurrences in extreme environments and an island-level checklist of this group
Figure 6. Diplacodes trivialis from coastal marsh site near Labuan Bajo, Flores Island, Lesser Sunda Archipelago, Indonesia: (A, C) females (RMBH: dried specimens; scale bar = 5 mm); and (B, D) tip of abdomen of the females.
Figure 2 in Revisiting the ideas of trees as templates and the competition paradigm in pairwise analyses of ground-dwelling ant species occurrences in a tropical forest
Figure 2 Presence probabilities of ant species in each tree species only for those one involved in nonrandom pairs for the two sampling techniques and seasons. PR: pitfall,rainy season; PD: pitfall, dry season; WR: Winkler, rainy season; WD: Winkler, dry season. GG= Guarea guidonia; IE= Inga edulis; NM= Nectandra membranacea; PG= Piptadenia gonoachanta.
First observational evidence of the relationship between the tropospheric temperature and cirrus cloud occurrence over India
<p>This dataset contains the normalized relative backscatter (NRB) coefficients and cloud fractions observed using Micro Pulse Lidar over Kattankulathur (12.82<sup>o</sup>N, 80.04<sup>o</sup>E ) presented in the paper.</p> <p> </p> <p> </p>
Figure 2 in Aedes aegypti queenslandensis: first geographic occurrence in Brazil and epidemiological implications
Figure 2 Comparative table between females of Aedes aegypti aegypti and Ae. aegypti queenslandensis.
Fig. 4 in First fossil record of Varanus (Reptilia, Squamata) from Switzerland and the earliest occurrences of the genus in Europe
Fig. 4 Parsimony-based character optimization on the tooth serrations based on the phylogeny of Pyron et al. (2013)
Fig. 2 in First fossil record of Varanus (Reptilia, Squamata) from Switzerland and the earliest occurrences of the genus in Europe
Fig. 2?Varanus sp. from Hüenerbach. a–f tooth NMBHüe.1 inlingual (a), labial (b), mesial (c), distal (d), occlusal (e), andventral (f) views; g–l) tooth NMBHüe.2 inlingual (g), labial (h), proximal (i), distal (j), occlusal (k), andventral (l) views
Fig. 3 in First fossil record of Varanus (Reptilia, Squamata) from Switzerland and the earliest occurrences of the genus in Europe
Fig. 3 Pulp cavity of extant varanoids. a–b Middle right dentary tooth (reversed) of Lanthanotus borneensis SMF 336 in lingual (a) and mesial (b) views. c–d Middle left dentary tooth (reversed) of Varanus indicus AMNH 58389 in lingual (c) and mesial (d) views. e–f Middle right maxilla tooth (inverted) of Varanus salvator PIMUZ A/III 1493 in lingual (e) and mesial (f) views
Fig. 5 in First fossil record of Varanus (Reptilia, Squamata) from Switzerland and the earliest occurrences of the genus in Europe
Fig. 5 Lacertidae indet. from Hüenerbach. Posterior portion of right maxilla NMB Hüe.3 in labial (a) and ventrolingual (b) views
Fig. 1 in First fossil record of Varanus (Reptilia, Squamata) from Switzerland and the earliest occurrences of the genus in Europe
Fig. 1 Location map of Hüenerbach by the city of Langnau im Emmental (Canton of Bern, Switzerland).The Swiss molasse Basin Tertiary Formations are marked highlighting the fact that the Hüenerbach locality is at the transition between the OMM and OSM. Ba. Basel, Be. Bern, Ge. Geneva, Zu. Zurich (modified after Mennecart, 2012)
Figure 8a–b in Abundance and Seasonal Occurrence of Pest Fruit Flies (Diptera: Tephritidae) in Residential and Rural Areas of Oahu (Hawaiian Islands)
Figure 8a–b. Mean captures of female C. capitata per trap per week in torula yeast traps at different sites (a), in different habitats (a, insert graph), and as monthly means throughout the trapping periods in different habitats (b). Values with the same letter in insert graph are not significantly different at the 0.05 level (Tukey's test, post ANOVA). F = 315.75; df = 6,27535; P <0.001; r2 = 6.44%; n = 228 (coffee), 2514 (gardens), 1807 (NW Oahu), 13230 (residential), 1658 (rural), 5630 (urban), 2475 (Waialua).
Figure 4a–b in Abundance and Seasonal Occurrence of Pest Fruit Flies (Diptera: Tephritidae) in Residential and Rural Areas of Oahu (Hawaiian Islands)
Figure 4a–b. Mean captures of female B. cucurbitae per trap per week in torula yeast traps at different sites (a), in different habitats (a, insert graph), and as monthly means throughout the trapping periods in different habitats (b). Values with the same letter in insert graph are not significantly different at the 0.05 level (Tukey's test, post ANOVA). F = 2897.68; df = 5,27536; P <0.001; r2 = 34.48%; n = 2514 (gardens), 1807 (NW Oahu), 13230 (residential), 1886 (rural), 5630 (urban), 2475 (Waialua).
Figure 3a–b in Abundance and Seasonal Occurrence of Pest Fruit Flies (Diptera: Tephritidae) in Residential and Rural Areas of Oahu (Hawaiian Islands)
Figure 3a–b. Mean captures of male B. cucurbitae per trap per week in cue-lure traps at different sites (a), in different habitats (a, insert graph), and as monthly means throughout the trapping periods in different habitats (b). Values with the same letter in insert graph are not significantly different at the 0.05 level (Tukey's test, post ANOVA). F = 5453.02; df = 5,18128; P <0.001; r2 = 60.06%); n = 2514 (gardens), 1807 (NW Oahu), 8879 (residential), 1720 (rural), 739 (urban), 2475 (Waialua).
Figure 7a–b in Abundance and Seasonal Occurrence of Pest Fruit Flies (Diptera: Tephritidae) in Residential and Rural Areas of Oahu (Hawaiian Islands)
Figure 7a–b. Mean captures of male C. capitata per trap per week in trimedlure traps at different sites (a), in different habitats (a, insert graph), and as monthly means throughout the trapping periods in different habitats (b). Values with the same letter in insert graph are not significantly different at the 0.05 level (Tukey's test, post ANOVA). F = 586.20; df = 6,18127; P <0.001; r2 = 16.25%; n = 228 (coffee), 2514 (gardens), 1807 (NW Oahu), 8879 (residential), 1492 (rural), 739 (urban), 2475 (Waialua).
Figure 2a–f in Abundance and Seasonal Occurrence of Pest Fruit Flies (Diptera: Tephritidae) in Residential and Rural Areas of Oahu (Hawaiian Islands)
Figure 2a–f. Overall mean (±SE) monthly captures of male B. cucurbitae in cue-lure traps (a), female B. cucurbitae in protein traps (b), male B. dorsalis in methyl eugenol traps (c), female B. dorsalis in protein traps (d), male C. capitata in trimedlure traps (e), and female C. capitata in protein traps, based on all trapping sites maintained on Oahu between April 2009 and December 2013.
Figure 9a–c in Abundance and Seasonal Occurrence of Pest Fruit Flies (Diptera: Tephritidae) in Residential and Rural Areas of Oahu (Hawaiian Islands)
Figure 9a–c. Correlation between mean monthly captures of female flies in protein traps and males in male lure traps for B. cucurbitae (a), B. dorsalis (b), and C. capitata (c).
Figure 6a–b in Abundance and Seasonal Occurrence of Pest Fruit Flies (Diptera: Tephritidae) in Residential and Rural Areas of Oahu (Hawaiian Islands)
Figure 6a–b. Mean captures of female B. dorsalis per trap per week in torula yeast traps at different sites (a), in different habitats (a, insert graph), and as monthly means throughout the trapping periods in different habitats (b). Values with the same letter in insert graph are not significantly different at the 0.05 level (Tukey's test, post ANOVA). F = 447.43; df = 5,27536; P <0.001; r2 = 7.51%; n = 2514 (gardens), 1807 (NW Oahu), 13230 (residential), 1886 (rural), 5630 (urban), 2475 (Waialua).
Figure 5a–b in Abundance and Seasonal Occurrence of Pest Fruit Flies (Diptera: Tephritidae) in Residential and Rural Areas of Oahu (Hawaiian Islands)
Figure 5a–b. Mean captures of male B. dorsalis per trap per week in methyl eugenol traps at different sites (a), in different habitats (a, insert graph), and as monthly means throughout the trapping periods in different habitats (b). Values with the same letter in insert graph are not significantly different at the 0.05 level (Tukey's test, post ANOVA). F = 1459.54; df = 5,18128; P <0.001; r2 = 28.70%; n = 2514 (gardens), 1807 (NW Oahu), 8879 (residential), 1720 (rural), 739 (urban), 2475 (Waialua).
Data for the publication "Significant Increase in Graupel and Lightning Occurrence in a Warmer Climate Simulated by Prognostic Graupel Parameterization"
<p>This dataset includes a set of 11yr simulations using the MIROC6 global aerosol-climate model under the pre-industrial (PI, aerosol emission at the year 1850), present-day (PD, aerosol emission at the year 2000), and future warming (SST+4K, a uniform 4 K increase in sea surface temperature) conditions.</p> <p>The data are used in the manuscript entitled "Significant Increase in Graupel and Lightning Occurrence in a Warmer Climate Simulated by Prognostic Graupel Parameterization".</p>
Fig. 7 in Notes on the Occurrence of Tintinnid Ciliates, and the Nasselarian Radiolarian Amphimelissa setosa of the Marine Microzooplankton, in the Chukchi Sea (Arctic Ocean) Sampled each August from 2011 to 2020
Fig. 7. The growth in the list of tintinnid species reported from the Chukchi Sea beginning with the first sampling in 1953 up to and including our 2020 sampling. The list of the 60 species now known for Chukchi Sea, with sampling year first found for each species, and the reference, is given in the supplementary file. Data are from Bursa 1963, Matsuno et al. 2014, Li et al. 2016, Yokoi et al. 2016, Dolan et al. 2017, Xu et al. 2018, Wang et al. 2019, and this study.
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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.