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Data for study "Direct Answers in Google Search Results"
<p>The goal of this research is to examine <strong>direct answers</strong> in Google web search engine. Dataset was collected using Senuto (<a href="https://www.senuto.com/">https://www.senuto.com/</a>). Senuto is as an online tool, that extracts data on websites visibility from Google search engine.</p> <p>Dataset contains the following elements:</p> <ol> <li>keyword,</li> <li>number of monthly searches,</li> <li>featured domain,</li> <li>featured main domain,</li> <li>featured position,</li> <li>featured type,</li> <li>featured url,</li> <li>content,</li> <li>content length.</li> </ol> <p>Dataset with visibility structure has <strong>743 798 keywords</strong> that were resulting in SERPs with direct answer.</p>
Supporting Information for Publication "Multi-band study of a bi-directional jet occurred in the upper chromosphere"
<p>This supporting information provides three observational movies from SDO/AIA, SDO/HMI, and IRIS. The evolution of the jet and the evolution of the line-of-sight magnetograms in the corresponding region can be tracked in these movies. The caption of each movie is included in 'AGUSupporting-Information_Movie.pdf'.</p>
Text-fig. 3. Distribution of main types of volcanoes in the NearShore Volcanic Belt of Eastern Sikhote-Alin' (Eocene–Neogene). 1 – Central volcanoes (partly preserved); 2 – Central volcanoes (destructed); 3 – Shield and gentle sloping volcanoes with a dolerite or trachy-basaltic neck on the top; 4 – Lava and scoria cones; 5 – Pyroclastic, tuffaceous coarse- and fine-grained terrigenous sedimentary rocks, partly with plant-bearing levels; 6 – Eruption centers of plateau-basalts and the direction of lava flows; 7 – Main Late Cenozoic basaltic plateaus; 8 – Fumarol fields; 9 – Hot springs. in Mid-Latitude Palaeogene Floras Of Eurasia Bound To Volcanic Settings And Palaeoclimatic Events - Experience Obtained From The Far East Of Russia (Sikhote-Alin') And Central Europe (Bohemian Massif)
Text-fig. 3. Distribution of main types of volcanoes in the NearShore Volcanic Belt of Eastern Sikhote-Alin' (Eocene–Neogene). 1 – Central volcanoes (partly preserved); 2 – Central volcanoes (destructed); 3 – Shield and gentle sloping volcanoes with a dolerite or trachy-basaltic neck on the top; 4 – Lava and scoria cones; 5 – Pyroclastic, tuffaceous coarse- and fine-grained terrigenous sedimentary rocks, partly with plant-bearing levels; 6 – Eruption centers of plateau-basalts and the direction of lava flows; 7 – Main Late Cenozoic basaltic plateaus; 8 – Fumarol fields; 9 – Hot springs.
Text-fig. 7. Projection of the declinations and inclinations of primary component of the DRM vectors and a mean direction based on Fisher statistics A – samples with normal polarity (down - projection on the lower hemisphere), B – samples with reversed polarity (up - projection on the upper hemisphere). in New Updated Results Of Paleomagnetic Dating Of Cave Deposits Exposed In Za Hájovnou Cave, Javoříčko Karst
Text-fig. 7. Projection of the declinations and inclinations of primary component of the DRM vectors and a mean direction based on Fisher statistics A – samples with normal polarity (down - projection on the lower hemisphere), B – samples with reversed polarity (up - projection on the upper hemisphere).
Figure 3 in The effects of various lake typologies on the distribution of Chironomus spp. (Diptera), and arguments on optional factors of Water Framework Directive in Türkiye
Figure 3. CCA ordination of the sampled lakes (L1 to L20, except L2), significant environmental variables and species. Environmental variables ranging over (VIF> 10) were omitted from the ordination. A total of 56.62% variance was expressed in the first two axes. Groups (Grp I–IV) spotted by using K-means algorithm were mapped on the biplot. ORP: oxidation and reduction potential.
Figure 4 in The effects of various lake typologies on the distribution of Chironomus spp. (Diptera), and arguments on optional factors of Water Framework Directive in Türkiye
Figure 4. CCA ordination of the sampled lakes (L1 to L20, except L2) based on national altitude class boundaries (R1: <800 m, R2: 800–1600 m, R3:>1600 m). A total of 62.06% variance was expressed in the first two axes. The distinction of the three groups was found to be statistically significant (p <0.05). For the significance levels of the typological factors, see Table 1.
Figure 2 in The effects of various lake typologies on the distribution of Chironomus spp. (Diptera), and arguments on optional factors of Water Framework Directive in Türkiye
Figure 2. Pearson's correlation heatmap of the 20 environmental variables and 2 taxa metrics (H` and J). Color intensity and the size of the circle are proportional to the correlation coefficients: red spectrum indicates a negative correlation, and blue spectrum indicates a positive correlation.
Figure 4 in Іnfluence of some heavy metals to the pulmonary and direct diffusive respiration of the great ramshorn Planorbarius corneus allospecies (Mollusca: Gastropoda: Planorbidae) from the Ukrainian river system
Figure 4. Photo of habitat Planorbarius corneus from Sula River (Romny, Sumy region) in 2021 (Photos: Yuliia V. Babych).
Figure 2 in Іnfluence of some heavy metals to the pulmonary and direct diffusive respiration of the great ramshorn Planorbarius corneus allospecies (Mollusca: Gastropoda: Planorbidae) from the Ukrainian river system
Figure 2. Map showing the type localities of Planorbarius corneus s. lato allospecies: black triangle – «western»; black square – «eastern».
Figure 3 in Іnfluence of some heavy metals to the pulmonary and direct diffusive respiration of the great ramshorn Planorbarius corneus allospecies (Mollusca: Gastropoda: Planorbidae) from the Ukrainian river system
Figure 3. Photo of habitat Planorbarius corneus from Hnyla River (Horodnytsia village, Ternopil region) in 2021 (Photos: Yuliia V. Babych).
Figure 1 in Іnfluence of some heavy metals to the pulmonary and direct diffusive respiration of the great ramshorn Planorbarius corneus allospecies (Mollusca: Gastropoda: Planorbidae) from the Ukrainian river system
Figure 1. Shells of Planorbarius corneus s. lato. (A – allospecies "western", B – allospecies "eastern"): 1 – top view; 2 – bottom view; 3 – side view. Scale bars: 10 mm. (Photos: Yuliia V. Babych).
Figure 11 in Paracossulus thrips (Hübner, 1818) (Cossidae) and Lignyoptera fumidaria (Hübner, 1825) (Geometridae) - two Lepidoptera genera new for Serbia with a review of the distribution of these two Habitats Directive species in the Balkan Peninsula
Figure 11. Distribution of Lignyoptera fumidaria in the Balkan Peninsula. Red dots represent the new localities; black dots – recently published localities; yellow dots – old published localities.
Figure 9 in Paracossulus thrips (Hübner, 1818) (Cossidae) and Lignyoptera fumidaria (Hübner, 1825) (Geometridae) - two Lepidoptera genera new for Serbia with a review of the distribution of these two Habitats Directive species in the Balkan Peninsula
Figure 9. Lignyoptera fumidaria male from Vidlič Mt., above Krupac Village, 525 m. Scale bar = 1 cm.
Figure 7 in Paracossulus thrips (Hübner, 1818) (Cossidae) and Lignyoptera fumidaria (Hübner, 1825) (Geometridae) - two Lepidoptera genera new for Serbia with a review of the distribution of these two Habitats Directive species in the Balkan Peninsula
Figure 7. Paracossulus thrips male from Vidlič Mt., above Gulenovci Village, 967 m. Scale bar = 1 cm.
Fig. 1. Pelomedusa galeata from the Ratelfontein farm near Calvinia observed directly after rainfall, 16 February 2019 in Mind the gap-Is the distribution range of Pelomedusa galeata really disjunct in western South Africa?
Fig. 1. Pelomedusa galeata from the Ratelfontein farm near Calvinia observed directly after rainfall, 16 February 2019. For the location of the farm, see Fig. 2 (locality 1). Photos: C.A. van Niekerk.
Fig. 3 in Relationship between host searching and wind direction in Ophraella communa (Coleoptera: Chrysomelidae)
Fig. 3. Mean numbers (± SE) of Ophraella communa eggs and adults at various cardinal directions from the center of each plot on common ragweed plants in the concentric bands. Data represented by columns bearing the same letters were not significantly different (LSD, a = 0.05). The dominant direction of the wind during the period of the entire experiment was from the south.
Fig. 1 in Relationship between host searching and wind direction in Ophraella communa (Coleoptera: Chrysomelidae)
Fig. 1. Plot design to study the location of host plants by Ophraella communa adults in relation to wind direction. This diagram displays the planting pattern for 1 m wide concentric plots of the host, common ragweed, separated by 1 m wide concentric barriers of a non-host, sunflower.
Fig. 2 in Relationship between host searching and wind direction in Ophraella communa (Coleoptera: Chrysomelidae)
Fig. 2. Wind roses at different dates observed by Changsha Meteorological Observatory from 5 Jul to 15 Aug 2010. The letters a, b, c, d, and e in each small figure represented general wind roses on 5–10 Jul, 11–20 Jul, 21–31 Jul, 1–10 Aug, and 11–15 Aug 2010, respectively.
Fig. 3 in Influence of plant direction, layer, and spacing on the infestation levels of Anthonomus eugenii (Coleoptera: Curculionidae) in open jalapeño pepper fields in North Florida
Fig. 3. Number of infested fruits and presence of weevil larvae in different jalapeño plant parts (means ± SE). Number of infested fruits in 5 directions (A), in 3 layers (C), and at 5 spacings (E). Number of larval A. eugenii within infested fruits in 5 directions (B), in 3 layers (D), and at 5 spacings (F). Different letters indicate significant differences among the treatments (means separated by Tukey's HSD, P <0.05).
Fig. 4 in Influence of plant direction, layer, and spacing on the infestation levels of Anthonomus eugenii (Coleoptera: Curculionidae) in open jalapeño pepper fields in North Florida
Fig. 4. Fruit wall thickness and single weight in different jalapeño plant parts (means ± SE). Fruit wall thickness (A) and single weight (B) in 5 directions, fruit wall thickness (C) and single weight (D) in 3 layers, fruit wall thickness (E) and single weight (F) at 5 spacings. Different letters indicate significant differences among the treatments (means separated by Tukey's HSD, P <0.05).
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.