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Figure 1 in Changes in galling insect community on Caryocar brasiliense trees mediated by soil chemical and physical attributes
Figure 1. Principal components regressions among: (A) abundance of galling insects (A.G.I.) with phosphorus-Mehlich 1 (mg dm-3) contents (P.C.) and sand (dag kg-1) (Sa.); (B) species richness of galling insects (S.R.G.I.) with capacity of cationic exchange (cmol dm-3) c (C.C.E.); (C) diversity of galling insects (D.G.I.) with C.C.E. and Sa.; (D) percentage of galled leaflet by all galls (P.G.L.) with pH in water and clay (dag kg-1) (Cl.); and (E) percentage of leaflet area taken by all galls (P.L.A.G.) with aluminum (cmol dm-3) contents (A.C.) and c C.C.E. on Caryocar brasiliense trees in three years. The symbols represent the averages and the bars the standard errors. n = 111.
Figure 4 in Changes in galling insect community on Caryocar brasiliense trees mediated by soil chemical and physical attributes
Figure 4. Principal components regressions among: (A) abundance of predators (A.Pr.) with phosphorus-Mehlich 1 (mg dm-3) contents (P.C.) and clay (dag kg-1) (Cl.); (B) species richness of predators (S.R.Pr.) with number of Hymenoptera discoid galls (H.D.G.), species richness of parasitoids (S.R.P.), and Cl.; (C) diversity of predators (D.Pr.) with diversity of parasitoids (D.P.) and Cl.; (D) number of Zelus armillatus (Zar.) with P.C., percentage of soil base saturation of the capacity of cationic exchange to pH 7.0 (S.B.S.), silt (dag kg-1) (Si.), numbers of Eurytoma sp. glodoid galls (E.G.G.), and capacity of cationic exchange (cmol dm-3) (C.C.E.); (E) number of Epipolops sp. (Epi.) c with protocooperanting ants (Ants), Cl., and pH in water; and (F) number of spiders (Spi.) with Ants, P.C., and Si. on Caryocar brasiliense trees in three years. The symbols represent the averages and the bars the standard errors. n = 111.
Figure 3 in Relations between soil attributes and the abundance of Bacillus thurigiensis in the Cerrado of Maranhão state, Brazil
Figure 3. Similarity dendrogram between iBt, chemical and physical soil attributes in the Maranhão eastern Cerrado. Notes: A: Group 1 (G1) in the red line cluster, Group 2 (G2) in the green line cluster, Group 3 (G3) in the purple line cluster. B: Legend of the abbreviations SM: São Mateus do Maranhão; AT: Alto Alegre; CT: Coroatá; TB: Timbiras; CD: Codó. Source: Authors.
Figure 2 in Relations between soil attributes and the abundance of Bacillus thurigiensis in the Cerrado of Maranhão state, Brazil
Figure 2. Biplot showing the association between iBt, chemical and physical attributes in soil samples in the Maranhão eastern Cerrado. Note: High Cos2 values are associated with a color scale and proximity to the circle of correlations; the warmer the color (red) and closer to the circle of correlation the greater the importance of these variables for the interpretation of these components. iBt: index of Bacillus thuringiensis; OM: organic matter; P: phosphorus; K: potassium; Na: sodium; Ca: calcium; Mg: magnesium; Al: aluminum; H+Al: potencial acidity; SB: sum of bases; CEC: cation exchange capacity; BS: base saturation; m: aluminum saturation.
Figure 5 in Effect of season and housing systems on various physiobehavioral attributes of local breed of rabbits (Oryctolagus cuniculus) in Southern Punjab, Pakistan
Figure 5. Effect of seasons on TSL of male rabbits under cage system. Data is mean (± SE) and different letters on the bars depict statistical difference at (p ≤ 0.05) for seasons.
Figure 4 in Effect of season and housing systems on various physiobehavioral attributes of local breed of rabbits (Oryctolagus cuniculus) in Southern Punjab, Pakistan
Figure 4. Effect of housing system on various physiological attributes of rabbits. Data is mean (± SE). Similar letters on the bars indicate non-significant (p ≥ 0.05) difference within caged and colony reared rabbits for rectal temperature. Different letters on the bars indicate significant (p ≤ 0.05) difference within caged and colony reared rabbits for respiration rate.
Figure 5. B in Phytochemical and biological attributes of Bauhinia variegata L. (Caesalpiniaceae)
Figure 5. B. variegata extracts result forα-amylase inhibition assay. The standard drug used is Acarbose IC50 33.43 ± 0.28 µg/mL. All procedures are repeated three times and results are mentioned as mean ± SD. nH = n-hexane; EA = ethyl acetate; MeOH = methanol; DW = distilled water; IC 50 = concentration for 50% inhibition; (S) = stem; (L) = leaf; (F) = flower; (B) = bark; (R) = root.
Figure 4 in Phytochemical and biological attributes of Bauhinia variegata L. (Caesalpiniaceae)
Figure 4. Brine shrimp lethality assay of B. variegata extracts. Doxorubicin is used as a standard with an LC50 5.63 ± 0.25 µg/ mL. All values are obtained thrice and shown as mean ± SD. nH = n-hexane; EA = ethyl acetate; MeOH = methanol; DW = distilled water; LC50 = concentration for 50% lethality; (S) = stem; (L) = leaf; (F) = flower; (B) = bark; (R) = root.
Figure 3 in Population attributes of Littoraria angulifera (Gastropoda: Littorinidae) in mangroves in Bahia State, northeastern Brazil
Figure 3. Total specimens of Littoraria angulifera collected monthly throughout 2018 on the grass Spartina alterniflora in a mangrove (M1) in Ilhéus, Bahia State, northeastern Brazil, distributed by size classes (shell height), being: C1 (less than 2.99 mm), C2 (3-5.9 mm), C3 (6-8.99 mm), C4 (9-11.99 mm), C5 (12-14.99 mm), C6 (15-17.99 mm) and C7 (18-20.99 mm); A-L: January to December.
Figure 1 in Population attributes of Littoraria angulifera (Gastropoda: Littorinidae) in mangroves in Bahia State, northeastern Brazil
Figure 1. Map of northeastern Brazil showing the location of the Bahia State and the sampling stations (M1 and M2).
Figure 2 in Population attributes of Littoraria angulifera (Gastropoda: Littorinidae) in mangroves in Bahia State, northeastern Brazil
Figure 2. Monthly absolute frequency of males and females of Littoraria angulifera collected throughout 2018 on trunks of Rhizophora mangle in two localities (A = M1; B = M2) in the coast of the Bahia State, northeastern Brazil.
Figure 9. NHMUK R9832 in New shell information and new generic attributions for the Egyptian podocnemidid turtles "Podocnemis" fajumensis (Oligocene) and "Podocnemis" aegyptiaca (Miocene)
Figure 9. NHMUK R9832, entoplastron of an indeterminate representative of Erymnochelyini (Pleurodira, Podocnemididae), from the lower or middle Eocene, found 25 km north-northeast of InTasit (Gao Region, Mali). (a) Ventral view. (b) Dorsal view.
Figure 1. AMNH 5086 in New shell information and new generic attributions for the Egyptian podocnemidid turtles "Podocnemis" fajumensis (Oligocene) and "Podocnemis" aegyptiaca (Miocene)
Figure 1. AMNH 5086, neotype of the podocnemidid turtle Shetwemys fajumensis comb. nov. (Erymnochelyini), from the lower Oligocene (Rupelian) of the Fayum Depression (Fayum Governorate, northern Egypt), in ventral (a) and dorsal (b) views.
Figure 4 in New shell information and new generic attributions for the Egyptian podocnemidid turtles "Podocnemis" fajumensis (Oligocene) and "Podocnemis" aegyptiaca (Miocene)
Figure 4. Plastral remains of the podocnemidid turtle Shetwemys fajumensis comb. nov. (Erymnochelyini), from the lower Oligocene (Rupelian) of the Fayum Depression (Fayum Governorate, northern Egypt). (a–b) NHMUK R3435, anterior plastral lobe, in ventral (a) and dorsal (b) views. (c–d) NHMUK R8441, plaster cast of the specimen CGM C8509, anterior plastral lobe, in ventral (c) and dorsal (d) views. (e–f) AMNH 5093, articulated epiplastra and entoplastron, in ventral (e) and dorsal (f) views. (g–h) SMNS 11233/6, anterior plastral lobe, in ventral (g) and dorsal (h) views. (i–j) NHMUK R3103, partial anterior plastral lobe, in ventral (i) and dorsal (j) views. (k–l) SMNS 11233/5, right hypoplastron, in ventral (k) and dorsal (l) views. (m–n) SMNS 11233/3, articulated left hypoplastron and xiphiplastron, in dorsal (m) and ventral (n) views, and detail of the outer ornamental pattern (o).
Figure 8 in New shell information and new generic attributions for the Egyptian podocnemidid turtles "Podocnemis" fajumensis (Oligocene) and "Podocnemis" aegyptiaca (Miocene)
Figure 8. Geographical (a) and stratigraphic (b) position of the type localities of all extinct representatives of Erymnochelyini (Pleurodira, Podocnemididae) currently known (1–6), and region where the only extant representative of this lineage lives (7): (1) JonquiŁres, Aude, France, Europe. Early Eocene. Type locality of Eocenochelus lacombiana. (2) Saint-Germain-en-Laye, Yvelines, France, Europe. Middle Eocene. Type locality of Eocenochelus eremberti. (3) Osona, Catalonia, Spain, Europe. Late Eocene. Type locality of Eocenochelus farresi. (4) North of Lake Qarun, Fayum Depression, Fayum Governorate, Egypt, Africa. Early Oligocene. Type locality of Shetwemys fajumensis comb. nov. (5) Moghra Oasis, Qattara Depression, Matruh Governorate, Egypt, Africa. Early Miocene. Type locality of Apeshemys aegyptiaca comb. nov. (6) Lothagam, southwest of Lake Turkana, Kenya, Africa. Late Miocene. Type locality of Kenyemys williamsi and Turkanemys pattersoni. (7) Western Madagascar, Africa, where the extant Erymnochelys madagascariensis lives. The identification of each taxon through the shell or through both the skull and the shell is indicated in (b). Panel (b) is modified from the fig. 1 of PØrez-García et al. (2017).
Figure 3 in New shell information and new generic attributions for the Egyptian podocnemidid turtles "Podocnemis" fajumensis (Oligocene) and "Podocnemis" aegyptiaca (Miocene)
Figure 3. Shell remains of the podocnemidid turtle Shetwemys fajumensis comb. nov. (Erymnochelyini), from the lower Oligocene (Rupelian) of the Fayum Depression (Fayum Governorate, northern Egypt). (a–c) SMNS 11233/2, partial carapace, in dorsal (a), ventral (b), and left lateral (c) views. (d) Ventral view of the anterior lobe the holotype of the species, currently lost, based on the fig. 2C in plate 8 of Andrews (1903). (e–g) SMNS 12647, plastron, in ventral (e), dorsal (f), and left lateral (g) views. (g') corresponds to an enlarged photograph of the posterior plastral lobe, in left lateral view, in which the thickness in the regions close to the hypo-xiphiplastral suture (in blue), between the pelvic scars (in green), and at the level of the anal notch (in red), have been represented by arrows (h–i), SMNS 12646, plastron, in ventral (h) and dorsal (i) views.
Figure 2 in New shell information and new generic attributions for the Egyptian podocnemidid turtles "Podocnemis" fajumensis (Oligocene) and "Podocnemis" aegyptiaca (Miocene)
Figure 2. Shell remains of the podocnemidid turtle Shetwemys fajumensis comb. nov. (Erymnochelyini), from the lower Oligocene (Rupelian) of the Fayum Depression (Fayum Governorate, northern Egypt). (a–f) AMNH 5087, carapace and partial plastron, in dorsal (a), ventral (b), anterior (c), posterior (d), left lateral (e), and right lateral (f) views. (g–h) SMNS 11233/1, partial carapace, in dorsal (g) and ventral (h) views.
Figure 6 in New shell information and new generic attributions for the Egyptian podocnemidid turtles "Podocnemis" fajumensis (Oligocene) and "Podocnemis" aegyptiaca (Miocene)
Figure 6. Plastron of the podocnemidid turtle Apeshemys aegyptiaca comb. nov. (Erymnochelyini), from the lower Miocene (Burdigalian) of the Qattara Depression (Matruh Governorate, northern Egypt). (a–d) Type specimen. (a) Drawing of the ventral view of the plastron, corresponding to fig. 2 on plate 1 of Andrews (1900). (b–c) Plastron of the plaster cast NHMUK R2927, corresponding to the holoplastotype of the specimen, in ventral (b) and dorsal (c) views. (d) Drawing of the dorsal view of the posterior area of the posterior plastral lobe, corresponding to fig. 3 on plate 1 of Andrews (1900). (e) Ventral view of the partial plastron of another shell, currently lost, based on fig. 21 of Fourteau (1920).
Fig. 2 in New remains attributable to the holotype of the sauropod dinosaur Neuquensaurus australis, with implications for saltasaurine systematics
Fig. 2. Holotypic sacrum of the sauropod Neuquensaurus australis (Lydekker, 1893), MLP Ly 1 and 7, from the Late Cretaceous of Neuquén, Argentina. Stereophotographs and line drawings in ventral view. The abbreviations (s1–s7) indicate sacral vertebral identity. Dashed lines indicate missing bone, and dotted lines indicate intervertebral sutures.
Fig. 1 in New remains attributable to the holotype of the sauropod dinosaur Neuquensaurus australis, with implications for saltasaurine systematics
Fig. 1. Holotypic sacrum of the sauropod Neuquensaurus australis (Lydekker, 1893), MLP Ly 1 and 7, from the Late Cretaceous of Neuquén, Argentina. Posterior view of sixth sacral vertebra and anterior view of seventh sacral vertebra showing corresponding matrix, which snaps together when the vertebrae are articulated. The abbreviations (s6–s7) indicate sacral vertebral identity. Dashed lines indicate missing bone.
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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.