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Figure 3 in Bacterial community associated with Culex quinquefasciatus Say, 1823 (Diptera: Culicidae) from an urban area in the Amazon, Brazil

Figure 3 Phylogenetic tree based on maximum likelihood method using MEGA 11. The numbers shown next to the branches correspond to the percentage of replicate trees that the taxa were clustered together in the bootstrap test (1000 replicates).

opencc-by-4.0May 2024View details →
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Figure 2 in Bacterial community associated with Culex quinquefasciatus Say, 1823 (Diptera: Culicidae) from an urban area in the Amazon, Brazil

Figure 2 Heatmap of sequences with taxonomic assignment to genus level. The color gradient (yellow to purple) represents abundance. Yellow: higher bacterial abundance. Purple: lowest bacterial abundance. Abundance legend corresponds log10(%).

opencc-by-4.0May 2024View details →
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Figure 1 in Bacterial community associated with Culex quinquefasciatus Say, 1823 (Diptera: Culicidae) from an urban area in the Amazon, Brazil

Figure 1 Bar chart of the relative abundance of each bacterial genus per sample. The black bar comprises the genera that show relative abundance of less than 1%.

opencc-by-4.0May 2024View details →
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Figure. Food preferences of Chinese mole shrew (Anourosorex squamipes) from an urban area. a, b, c, d. Mean relative consumption along six trials for each food set are shown in a, b, c, d, respectively. (see materials and methods for details on the calculation of relative consumption). in Natural animal food preference of Chinese mole shrew (Anourosorex squamipes) from an urban area: a laboratory study

Figure. Food preferences of Chinese mole shrew (Anourosorex squamipes) from an urban area. a, b, c, d. Mean relative consumption along six trials for each food set are shown in a, b, c, d, respectively. (see materials and methods for details on the calculation of relative consumption).

opencc-by-4.0Dec 2020View details →
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Figure 5 in Effect of urban habitats on colony size of ants (Hymenoptera, Formicidae) In memory of Professor A. A. Zakharov (Russian Academy of Sciences, Moscow)

Figure 5. Colony size of species per different geographic area. A – Crematogaster subdentata; B – Lasius neglectus.

opencc-by-4.0Dec 2021View details →
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Figure 4 in Effect of urban habitats on colony size of ants (Hymenoptera, Formicidae) In memory of Professor A. A. Zakharov (Russian Academy of Sciences, Moscow)

Figure 4. Colony size of 9 species of ants in several habitats of the same geographic area (calculated according to (A. Zakharov, 1978, 2015). A – Lasius fuliginosus; B – Camponotus vagus; C – Lasius emarginatus; D – Lasius niger; E – Formica cinerea; F - Dolichoderus quadripunctatus; G – Lasius brunneus; H – Crematogaster subdentata; I – Lasius neglectus.

opencc-by-4.0Dec 2021View details →
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Figure 2 in Effect of urban habitats on colony size of ants (Hymenoptera, Formicidae) In memory of Professor A. A. Zakharov (Russian Academy of Sciences, Moscow)

Figure 2. Calculated curve of the size of the ant colony by the intensity of movement of foragers per 1 min along the trail (counting only in one direction, Zakharov, 1979; 2015). Within 14–140 - according to A. Zakharov (1979), from 184 to 307 - our data, with an additional calculation formula in this range of values.

opencc-by-4.0Dec 2021View details →
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Figure 3 in Effect of urban habitats on colony size of ants (Hymenoptera, Formicidae) In memory of Professor A. A. Zakharov (Russian Academy of Sciences, Moscow)

Figure 3. Colony size in 21 ant species, calculated by the formula of A. Zakharov (1979; 2015). Ukraine: A – Kyiv region, deciduous (Kd) and coniferous (Kp) forests, natural habitats; B – Kyiv, suburban habitats (Ks); C – Kyiv city, urban habitats; D – natural habitats in Crimea (C1 – mountain steppes, C2 – mountain meadows) and in the Carpathians (Carp, mountain meadows); Crimea, steppe areas, natural habitats (C_aet); suburban and urban habitats in Crimea (L_neg, C_sub); Crimea, oak-pistachio-juniper forests, natural habitats (P_tau; F_gag; C_sch); Russian Federation: E, F – Rostov-on-Don, suburban (L_neg_R2) and urban (L_neg_R1; C_sub_R1) habitats; Uzbekistan: G – natural (riparian forests, C_sub_tu) and urban (Tashkent city, everything else) habitats; Russian Federation: H – Ural, natural habitats (taiga). Ant species: L_pla – Lasius platythorax; Dol – Dolichoderus quadripunctatus; L_ful – Lasius fuliginosus; L_ema – Lasius emarginatus; L_bru – Lasius brunneus; F_ruf – Formica rufa; L_nig – Lasius niger; F_cin – Formica cinerea; C_vag – Camponotus vagus; C_aet – Camponotus aethiops; F_tru – Formica truncorum; F_pol – Formica polyctena; L_neg – Lasius neglectus; F_pra – Formica pratensis; P_tau – Plagiolepis tauricus; F_gag – Formica gagates; C_sch – Crematogaster schmidti; C_sub – Crematogaster subdentata; M_ber – Myrmica bergi; P_pal – Plagiolepis pallescens; F_aqu – Formica aquilonia.

opencc-by-4.0Dec 2021View details →
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Figure 1. D in Effect of urban habitats on colony size of ants (Hymenoptera, Formicidae) In memory of Professor A. A. Zakharov (Russian Academy of Sciences, Moscow)

Figure 1. D Locations of the study. Ukraine: 1 – Crimea (the Main ridge of the Mountainous Crimea and the South Coast, Saki region), 2 – Kyiv and Kyiv region, 3 – Carpathians; Uzbekistan: 4 – Tashkent city, tugai forests; Russian Federation: 5 – Ural, 6 – Rostov-on-Don city and region. Habitats. a – natural, b – suburban, c – urban.

opencc-by-4.0Dec 2021View details →
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Figure 2. The adult female with a in Different shades of snake: Peculiar coloration in an urban population of the Grass Snake, Natrix natrix (Linnaeus, 1758

Figure 2. The adult female with a peculiar blue coloration. From the top to bottom: blue coloration present at the margin of the last row of dorsal scales and ventral scales. The white underside of the throat is clearly visible; Dorsal view of the individual; The ventral color switches from white to black towards the tail and the blue color intensifies.

opencc-by-4.0Feb 2021View details →
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Figure 1. A in Different shades of snake: Peculiar coloration in an urban population of the Grass Snake, Natrix natrix (Linnaeus, 1758

Figure 1. A melanistic individual (top) and an individual from the subspecies N. n. persa (middle). A common occurring individual with black spots behind the head (bottom) captured at the locality.

opencc-by-4.0Feb 2021View details →
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Fig. 1 in Borrelia miyamotoi infection in Apodemus spp. mice populating an urban habitat (Warsaw, Poland)

Fig. 1. Scheme of the study area (city of Warsaw, Poland) showing the arrangement of mice-trapping locations. Black points – locations where B. miyamotoi infected mice were present; White points – locations where none of the captured mice were B. miyamotoi infected; N1–N3 – locations within northern suburbs; C1–C5 - locations within city centre; S1–S2 – locations within southern suburbs; numbers in boxes – B. miyamotoi prevalence in mice inhabiting respective areas.

opencc-by-4.0Apr 2021View details →
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Fig. 6 in Diversity and microhabitat use of benthic invertebrates in an urban forest stream (Southeastern Brazil)

Fig. 6. NMDS ordination (stress = 0.18) of each microhabitat type (litter, sand, and stone) sampled at the Tijuca River, located at the Tijuca Forest, Rio de Janeiro, Brazil.

opencc-by-4.0Oct 2021View details →
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Fig. 4. Rarefaction curves with extrapolations and 95 in Diversity and microhabitat use of benthic invertebrates in an urban forest stream (Southeastern Brazil)

Fig. 4. Rarefaction curves with extrapolations and 95% of confidence intervals for both the total sampling and each type of microhabitat of benthic invertebrates of Tijuca River, located at the Tijuca Forest, Rio de Janeiro, Brazil.

opencc-by-4.0Oct 2021View details →
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Fig. 5 in Diversity and microhabitat use of benthic invertebrates in an urban forest stream (Southeastern Brazil)

Fig. 5. Boxplot of the ecological descriptors calculated for each microhabitat type (litter, sand, and stone) with the one-way repeated measure ANOVA results and the Tukey pairwise post hoc test (letters). Different letters denote significant difference results (p <0.001).

opencc-by-4.0Oct 2021View details →
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Figs 1-3 in Diversity and microhabitat use of benthic invertebrates in an urban forest stream (Southeastern Brazil)

Figs 1-3. Sampled stretches of the Tijuca River, Tijuca Forest, Rio de Janeiro, Brazil: Figs 1, 2, first stretch located at 380 meters of altitude; and Fig. 3, second stretch located at 420 meters of altitude.

opencc-by-4.0Oct 2021View details →
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Figs 1, 2 in Nesting biology of the oil-collecting bee Epicharis (Hoplepicharis) fasciata (Hymenoptera: Apidae) in an urban area of Rio de Janeiro, RJ, Brazil

Figs 1, 2. Construction and nests of Epicharis (Hoplepicharis) fasciata Lepeletier & Serville, 1828 at the Jardim Botânico of Rio de Janeiro:1, female constructing her nest; 2, female inside her nest and another flying in the nesting area.

opencc-by-4.0Oct 2020View details →
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Figs 6, 7 in Nesting biology of the oil-collecting bee Epicharis (Hoplepicharis) fasciata (Hymenoptera: Apidae) in an urban area of Rio de Janeiro, RJ, Brazil

Figs 6, 7. Insects associated with Epicharis (Hoplepicharis) fasciata Lepeletier & Serville, 1828: 6, female of the cleptoparasitic bee Rhathymus bicolor Lepeletier & Serville, 1828 leaving a nest;7, female of Pseudomethoca sp. walking through the nesting area.

opencc-by-4.0Oct 2020View details →
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Figs 4, 5 in Nesting biology of the oil-collecting bee Epicharis (Hoplepicharis) fasciata (Hymenoptera: Apidae) in an urban area of Rio de Janeiro, RJ, Brazil

Figs 4, 5. Brood cells and larva of Epicharis (Hoplepicharis) fasciata Lepeletier & Serville, 1828: 4, lateral view (scale bar 1 cm); 5, brood cell with pre-defecating larva eating the pollen mass (scale bar 1 cm).

opencc-by-4.0Oct 2020View details →
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Fig. 3 in Nesting biology of the oil-collecting bee Epicharis (Hoplepicharis) fasciata (Hymenoptera: Apidae) in an urban area of Rio de Janeiro, RJ, Brazil

Fig. 3. Nests of Epicharis (Hoplepicharis) fasciata Lepeletier & Serville, 1828 showing the position of the brood cells.

opencc-by-4.0Oct 2020View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record