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Fig. 2 in Molecular and physiological characterization of the chitin synthase B gene isolated from CUlex pipieNS palleNS (Diptera: Culicidae)
Fig. 2 Expression profiles of CpCHSB in different tissues of fourth-instar C. pipiens pallens larvae. Tissues include head (HE), foregut (FG), midgut (MG), hindgut (HG), Malpighian tubules (MT) and carcass (CA). Relative expression levels were calculated based on the lowest expression value, which was ascribed an arbitrary value of 1. Results are shown as the mean ± SE
Fig. 1 in Molecular and physiological characterization of the chitin synthase B gene isolated from CUlex pipieNS palleNS (Diptera: Culicidae)
Fig. 1 Alignment of the conserved catalytic domain of chitin synthases from three mosquito species Seven characteristic motifs (M1–M7) in insect chitin synthases are highlighted. Dashes are used to denote gaps introduced to maximise alignment. Abbreviations: Ae, Aedes aegypti; Ag, Anopheles gambiae; Cp, Culex pipiens pallens
Fig. 4 in Isolation of infectious Theileria parva sporozoites secreted by infected Rhipicephalus appendiculatus ticks into an in vitro tick feeding system
Fig. 4 Demonstration of infectivity of secreted T. parva sporozoites collected from the in vitro tick feeding system. a Flow cytometric detection of cultured T. parva-infected lymphocytes. b Immunocytochemistry demonstrating T. parva schizont formation in bovine lymphocytes. Lymphocytes were probed with monoclonal antibodies: left panel, isotype control; right panel, anti-PIM. Red indicates antibody-specific reactivity to T. parva within bovine lymphocytes. Scale bar: 20 µm
Fig. 3 in Isolation of infectious Theileria parva sporozoites secreted by infected Rhipicephalus appendiculatus ticks into an in vitro tick feeding system
Fig. 3 Immunohistochemical detection of T. parva salivary gland acinus colonization in adult ticks. Tick sections were probed with monoclonal antibodies: a anti-PIM; b anti-p67; c isotype control. Red indicates antibody-specific reactivity to T. parva colonies. Scale bar: 50 µm
Fig. 1 in Isolation of infectious Theileria parva sporozoites secreted by infected Rhipicephalus appendiculatus ticks into an in vitro tick feeding system
Fig. 1 Infection of R. appendiculatus via acquisition feeding on a T. parva-infected calf. a Calf was infected via subcutaneous inoculation with T. parva salivary gland stabilate. The calf developed severe fever beginning 10 days post-infection. Red arrow indicates nymphal tick application and green arrows indicate collection of replete nymphs. b Detection of T. parva via p104 PCR. Amplicons were visualized in 2% agarose gel
Figure 1 in Amazonian soil fungi are efficient degraders of glyphosate herbicide; novel isolates of Penicillium, Aspergillus, and Trichoderma
Figure 1. Mass spectrum resulting from the HPLC-MS of the isolated Penicillium 4A21 filtered. The filtrate presents possible peaks of glyphosate (170.07), AMPA (112.13) and sarcosine (89).
Figure 3 in Filtrates from cultures of endophytic fungi isolated from leaves of Copaifera oblongifolia (Fabaceae) affect germination and seedling development differently
Figure 3. Variations (mean ± standard error) of aerial mass (A), root mass (B) and total seedling mass (C) of Copaifera oblongifolia as a function of treatments with inoculation of different species of endophytic fungi. Different letters on the bars indicate statistical variations between treatments (P <0.05) according contrast analysis
Figure 1 in Filtrates from cultures of endophytic fungi isolated from leaves of Copaifera oblongifolia (Fabaceae) affect germination and seedling development differently
Figure 1. Variations (mean ± standard error) of the germination percentage (A) and the time required for germination (B) of Copaifera oblongifolia seeds as a function of treatments with inoculation of different species of endophytic fungi. Different letters on the bars indicate statistical variations between treatments (P <0.05) according contrast analysis.
Figure 4 in Filtrates from cultures of endophytic fungi isolated from leaves of Copaifera oblongifolia (Fabaceae) affect germination and seedling development differently
Figure 4. The relationship between aerial mass (A), root mass (B) and total seedling mass (C) with seed mass of Copaifera oblongifolia.
SI Figure 2: Compositional differences among bacterial microinvertebrate external and internal microbiomes as well as mats they were isolated from using Bray Curtis distance matrix visualized with a NMDS ordination. Circles indicate each community and stars show centroids of microbiome types for each animal host. All host microbiomes (internal and external) are distinct from mat communities (P<0.05), but external microbiomes are more similar to mats than internal microbiomes are to mats. in External and internal microbiomes of Antarctic nematodes are distinct, but more similar to each other than the surrounding environment
SI Figure 2: Compositional differences among bacterial microinvertebrate external and internal microbiomes as well as mats they were isolated from using Bray Curtis distance matrix visualized with a NMDS ordination. Circles indicate each community and stars show centroids of microbiome types for each animal host. All host microbiomes (internal and external) are distinct from mat communities (P<0.05), but external microbiomes are more similar to mats than internal microbiomes are to mats.
Figure 5 in Delatylus andersoni n. gen., n. sp. (Nematoda: Neotylenchidae) Isolated from White Pine (Pinus monticola) Lumber from USA and Intercepted in Ningbo, China
Figure 5: Phylogeny of Delatylus andersoni n. gen., n. sp. and closely related inferred from partial 18 S rRNA gene sequences by Bayesian analysis. Phylogeny was inferred under a GTR + I + G model (−lnL = 6333.834; AIC = 12687.668; freqA = 0.2384; freqC = 0.2036; freqG = 0.267; freqT = 0.2911; R(a) = 1.1233; R(b) = 3.698; R(c) = 2.4739; R(d) = 0.7402; R(e) = 5.1375; R(f) = 1; Pinva = 0.6096; Shape = 0.8015). Posterior probability values exceeding 50% are given on appropriate clades.
Figure 2 in Delatylus andersoni n. gen., n. sp. (Nematoda: Neotylenchidae) Isolated from White Pine (Pinus monticola) Lumber from USA and Intercepted in Ningbo, China
Figure 2: Micrographs of females of Delatylus andersoni n. gen., n. sp: (A) entire body; (B) head region, (C) pharynx (arrow showing the position of excretory pore and hemizonid), (D) pharynx with anterior part of the gonad, (E) posterior part of the female body, (F, G) female tail (arrow showing the position of vulva and anus), H: lateral lines. (scale bars = 10 μm).
Figure 6 in Delatylus andersoni n. gen., n. sp. (Nematoda: Neotylenchidae) Isolated from White Pine (Pinus monticola) Lumber from USA and Intercepted in Ningbo, China
Figure 6: Phylogeny of Delatylus andersoni n. gen., n. sp. and closely related inferred from 28 S D2/D3 rRNA gene sequences by Bayesian analysis. Phylogeny was inferred under a TrN+G model (−lnL = 2644.97; AIC = 5301.9399; freqA = 0.2103; freqC = 0.1993; freqG = 0.3249; freqT = 0.2655; R(a) = 1; R(b) = 3.0953; R(c) = 1; R(d) = 1; R(e) = 7.2585; R(f) = 1; Pinva = 0; Shape = 0.3542). Posterior probability values exceeding 50% are given on appropriate clades.
Figure 4 in Delatylus andersoni n. gen., n. sp. (Nematoda: Neotylenchidae) Isolated from White Pine (Pinus monticola) Lumber from USA and Intercepted in Ningbo, China
Figure 4: SEM of Delatylus andersoni n. gen., n. sp. (A, B) En face view of head and lip (aa arrows point to the amphid aperture; oa arrows point to the oral aperture; op arrows point to outer labial papillae; (C) vulva, anus, and tail; (D) lateral fields.
Figure 3 in Delatylus andersoni n. gen., n. sp. (Nematoda: Neotylenchidae) Isolated from White Pine (Pinus monticola) Lumber from USA and Intercepted in Ningbo, China
Figure 3: Micrographs of valve at the pharyngeal–intestinal junction of females of Delatylus andersoni n. gen., n. sp.
Fig. 7 in Evaluating the utility of linear measurements to identify isolated tooth loci of extinct Hyracoidea
Fig. 7. Simulated and observed values of Borges et al.'s (Borges et al. 2019) δ values for simulated trait distributions on the tree in Fig. 1 for sets of traits (A, m1: m2 length; B, M1: M2 length; C, M2: M3 length) that show phylogenetic signal (red triangles) and phylogenetic retention (gray circles).
Fig. 2 in Evaluating the utility of linear measurements to identify isolated tooth loci of extinct Hyracoidea
Fig. 2. Illustration of measurements taken on lower (m1–m3, A–C) and upper (M1–M3, D–F) teeth in occlusal views to calculate potentially diagnostic traits. Measurements are illustrated on specimen UMZC H5101A, Procavia capensis. Abbreviations: LE, length; MW, width of the crown at metaloph; PW width of the crown at paraloph.
Fig. 6 in Evaluating the utility of linear measurements to identify isolated tooth loci of extinct Hyracoidea
Fig. 6. Overlap in potentially diagnostic trait values for upper molar loci of three example hyracoid taxa (A1, B1, Procavia capensis; A2, B2, Saghatherium bowni; A3, B3, Thyrohyrax meyeri). A. Length vs. proportional frequency, showing how a single trait, length, would be modeled in a univariate discriminant analysis using observed means and variances. Colored sections of the distributions show length values that are within 95% confidence intervals of the means of more than one tooth locus, indicating regions of ambiguous lengths. B. Length vs. relative width, showing scatter plots overlaid on 2D density diagrams showing the distribution of values for individual teeth.
Fig. 8 in Evaluating the utility of linear measurements to identify isolated tooth loci of extinct Hyracoidea
Fig. 8. Overlap in potentially diagnostic trait values for a case study of isolated molars of Meroehyrax kyongoi. In contrast to Fig. 4, molar locus identifications are based on occupation of space in this scatterplot. Question marks are overlaid over two specimens whose inferred tooth position conflicts with published diagnoses. In parentheses original identification in publication.
Fig. 1 in Evaluating the utility of linear measurements to identify isolated tooth loci of extinct Hyracoidea
Fig. 1. Phylogenetic tree and tooth size distribution in hyracoids (topology from Cooper et al. 2014). Taxa are time-scaled along the x-axis of the tree to reflect fossil occurrences based on the literature, with branches rescaled between these tip dates and a root age estimated at 70.1 million years. Taxa in bold text were included in analyses. Minimum monophyletic clade including taxa in bold indicates the range of the phylogenetic bracket applied for both length and width measures (base of clade indicated by black star). Minimum monophyletic clade for length measures from the literature is indicated by a white star at the base of the clade. Shapes to the right of tips indicate whether there is a significant fit with a model of ascending (increasing) tooth size down the molar row. Abbreviations: M, upper molars; m, lower molars.
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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.