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3,427 results for “Nematoda”
Figure 3 in A new species of the genus Ethmolaimus de Man, 1880 (Nematoda, Ethmolaimidae) from intertidal zone of the Yellow Sea, China
Figure 3. Ethmolaimus multispiralis sp. nov. A. Lateral view of entire female; B. Anterior end of female, showing amphidial fovea (arrow) and cuticle punctation; C. Pharyngeal region of female, showing buccal cavity, anterior and posterior pharyngeal bulbs, and excretory system (arrows). Scale bars: A = 50 µm; B = 10 µm; C = 20 µm.
Figure 9 in Meloidogyne paramali n. sp. (Nematoda: Meloidogyninae) and First Report of M. marylandi in maple and yacca tree from Japan
Figure 9: Phylogenetic relationships of the Melodidogyne paramali n. sp. within the genus Meloidogyne as inferred from Bayesian analysis of the intergenic region between CO II and 16S rDNA sequences using the GTR + G model (ln L = −9,869.8599; freqA = 0.3676; freqC = 0.0265; freqG = 0.0939; freqT = 0.5121; R(a) = 3.2156; R(b) = 5.9094; R(c) = 1.5251; R(d) = 2.6383; R(e) = 13.9890; R(f) = 1.0000; Shape = 0.6340). Posterior probabilities are given in clades node. Newly obtained sequences are indicated in bold and the sequence codes are given in specimen-clone.
Figure 6 in Meloidogyne paramali n. sp. (Nematoda: Meloidogyninae) and First Report of M. marylandi in maple and yacca tree from Japan
Figure 6: Phylogenetic relationships of the Melodidogyne paramali n. sp. within the genus Meloidogyne as inferred from Bayesian analysis of the 18S rDNA sequences using the SYM + I + G model (ln L = −9,656.5775; freqA = 0.2500; freqC = 0.2500; freqG = 0.2500; freqT = 0.2500; R(a) = 1.1490; R(b) = 2.9493; R(c) = 1.9703; R(d) = 0.5777; R(e) = 4.7703; R(f) = 1.0000; Pinva = 0.4140; Shape = 0.4400). Posterior probabilities are given in clades node. Newly obtained sequences are indicated in bold and the sequence codes are given in specimen-clone.
Figure 4 in Meloidogyne paramali n. sp. (Nematoda: Meloidogyninae) and First Report of M. marylandi in maple and yacca tree from Japan
Figure 4: Light photomicrographs of host plant roots infected by Meloidogyne paramali n. sp. and female. A: Root-knot; B: Female.
Figure 5 in Meloidogyne paramali n. sp. (Nematoda: Meloidogyninae) and First Report of M. marylandi in maple and yacca tree from Japan
Figure 5: Light photomicrographs of Meloidogyne marylandi J2. A: Entire body; B, C: Anterior region; D: Lateral region; E–H: Tail region. (Scale bars = 10 μm).
Figure 3 in Meloidogyne paramali n. sp. (Nematoda: Meloidogyninae) and First Report of M. marylandi in maple and yacca tree from Japan
Figure 3: Light photomicrographs of Meloidogyne paramali n. sp. male and female. A: Male head region; B: Male lateral region; C: Male tail region; D–H: Female perineal patterns. (Scale bars = 10 μm).
Figure 2 in Meloidogyne paramali n. sp. (Nematoda: Meloidogyninae) and First Report of M. marylandi in maple and yacca tree from Japan
Figure 2: Light photomicrographs of Meloidogyne paramali n. sp. J2. A: Entire body; B: Anterior region; C: Post median bulb region; D: Lateral region; E–K: Tail region. (Scale bars = 10 μm).
Figure 1 in Meloidogyne paramali n. sp. (Nematoda: Meloidogyninae) and First Report of M. marylandi in maple and yacca tree from Japan
Figure 1: Meloidogyne paramali n. sp. A: J2; B: Anterior region of J2; C: Anterior region of male; D: Lateral region of male; E: Lateral region of J2; F: Male tail region; G: Variations of J2 tail; H, I: Female perineal patterns. (Scale bars = 10 μm).
Figure 7 in Meloidogyne paramali n. sp. (Nematoda: Meloidogyninae) and First Report of M. marylandi in maple and yacca tree from Japan
Figure 7: Phylogenetic relationships of the Melodidogyne paramali n. sp. within the genus Meloidogyne as inferred from Bayesian analysis of the ITS region of rDNA sequences using the GTR+ G model (ln L = –15,611.9209; freqA = 0.2778; freqC = 0.1784; freqG = 0.2084; freqT = 0.3354; R(a) = 1.1160; R(b) = 2.3301; R(c) = 1.4759; R(d) = 0.7128; R(e) = 2.9133; R(f) = 1.0000; Shape = 0.5730). Posterior probabilities are given in clades node. Newly obtained sequences are indicated in bold and the sequence codes are given in specimen-clone.
Figure 8 in Meloidogyne paramali n. sp. (Nematoda: Meloidogyninae) and First Report of M. marylandi in maple and yacca tree from Japan
Figure 8: Phylogenetic relationships of the Melodidogyne paramali n. sp. within the genus Meloidogyne as inferred from Bayesian analysis of the D2–D3 region of the 28S rDNA sequences using the TVM + I + G model (ln L = –9,976.1624; freqA = 0.2157; freqC = 0.1943; freqG = 0.2737; freqT = 0.3163; R(a) = 1.1061; R(b) = 3.8613; R(c) = 1.8155; R(d) = 0.4745; R(e) = 3.8613; R(f) = 1.0000; Pinva = 0.2180; Shape = 0.7340). Posterior probabilities are given in clades node. Newly obtained sequences are indicated in bold and the sequence codes are given in specimen-clone.
Figure 4 in Morphological and Molecular Characterization of Punctodera stonei Brzeski, 1998 (Nematoda: Heteroderidae) from Virginia, USA
Figure 4: Phylogenetic relationships within the genus Punctodera: Bayesian 50% majority rule consensus tree from two runs, as inferred from analysis of the COI gene sequence alignment under the GTR + I + G model. Posterior probabilities and bootstrap values ≥70% are given for appropriate clades. New sequences are indicated by bold font.
Figure 1 in Morphological and Molecular Characterization of Punctodera stonei Brzeski, 1998 (Nematoda: Heteroderidae) from Virginia, USA
Figure 1: Photomicrographs of cysts, vulval cones, and J2 of P. stonei from Virginia. A, B: Anterior ends of J2s; C: Excretory pore and hemizonid with arrow pointing toward hemizonid; D, E: Entire cysts with D showing both fenestra in the middle; F: Cyst posterior part showing vulval and anal fenestrae; G: Lateral field with four incisures for J2; H, I: Tails of J2s with arrow pointing toward the anal area in I.J2, second-stage juveniles.
Figure 5 in Rotylenchus wimbii n. sp. (Nematoda: Hoplolaimidae) associated with finger millet in Kenya
Figure 5: BI phylogenetic tree generated from the analysis of COI of mtDNA sequences using GTR + G + I nucleotide substitution model. Bayesian posterior probabilities are given next to each node and sequences of Rotylenchus wimbii n. sp. are in bold.
Figure 3 in Rotylenchus wimbii n. sp. (Nematoda: Hoplolaimidae) associated with finger millet in Kenya
Figure 3: BI phylogenetic tree generated from the analysis of D2-D3 of 28S rDNA sequences using GTR + G + I nucleotide substitution model. Bayesian posterior probabilities are given next to each node and sequences of Rotylenchus wimbii n. sp. are in bold.
Figure 4 in Rotylenchus wimbii n. sp. (Nematoda: Hoplolaimidae) associated with finger millet in Kenya
Figure 4: BI phylogenetic tree generated from the analysis of ITS of rDNA sequences using GTR + G + I nucleotide substitution model. Bayesian posterior probabilities are given next to each node and sequences of Rotylenchus wimbii n. sp. are in bold.
Figure 1 in Description of Laimaphelenchus sinensis n. sp. (Nematoda: Aphelenchoididae) from declining Chinese pine, Pinus tabuliformis in Beijing, China
Figure 1: Line drawings of LaimaphelenChus sinensis n. sp. A: Entire female; B: Entire male; C: Anterior region; D: Female posterior region showing vulva and post-uterine sac; E: Lateral lines F, G: Female tail terminus; H: Male tail; I: Spicule. (Scale bars = A, B = 20µ m; C-I = 10µ m).
Figure 3 in Description of Laimaphelenchus sinensis n. sp. (Nematoda: Aphelenchoididae) from declining Chinese pine, Pinus tabuliformis in Beijing, China
Figure 3: Phylogenetic relationships of LaimaphelenChus sinensis n. sp. and aphelenchid nematodes based on full length of 18 S rDNA. The 100001st Bayesian tree inferred from 18 S rDNA under TVM + I + G model. AphelenChus avenae (JQ348399) served as the outgroup species. Posterior probability values exceeding 50% are given on appropriate clades.
Figure 3 in Morphological and Molecular Characterization of Punctodera stonei Brzeski, 1998 (Nematoda: Heteroderidae) from Virginia, USA
Figure 3: Phylogenetic relationships within the genus Punctodera: Bayesian 50% majority rule consensus tree from two runs, as inferred from analysis of the ITS rRNA gene sequence alignment under the GTR + I + G model. Posterior probabilities and bootstrap values ≥70% are given for appropriate clades. New sequences are indicated by bold font. *Identified as P. punctata in the GenBank and by Sabo et al. (2002).
Figure 2 in Description of Laimaphelenchus sinensis n. sp. (Nematoda: Aphelenchoididae) from declining Chinese pine, Pinus tabuliformis in Beijing, China
Figure 2: Light photomicrographs of LaimaphelenChus sinensis n. sp. A: Entire female; B: Entire male; C: Lateral lines; D: Anterior region; E: Female posterior region showing vulva and postuterine sac; F, G: Vulval regions; H: Female tail; I-K: Female tail terminus; L-N: Male tails arrows showing position of caudal papillae (Scale bars = A, B = 20 µm; C-N = 10µ m; Abbreviations: ex, excretory pore).
Figure 7 in A new rare nematode Nothocriconemoides hangzhouensis n. sp. (Nematoda: Criconematidae) from Hangzhou, China
Figure 7: Phylogenetic relationships of Nothocriconemoides hangzhouensis n. sp. with other criconematids species as inferred from Bayesian analysis using the ITS rRNA gene sequence dataset with the GTR + I + G model (−lnL=7727.9982; AIC = 15603.9963; freqA=0.2067; freqC=0.2560; freqG=0.2814; freqT=0.2559; R(a)=1.5781; R(b)=2.9918; R(c)=1.7856; R(d)=0.6423; R(e)=2.8799; R(f)=1.0000; Pinva=0.0460; and Shape=0.6180). Posterior probability more than 70% is given for appropriate clades. Newly obtained sequences are indicated in bold.
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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.