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3,427 results for “Nematoda”
Figure 8 in A new rare nematode Nothocriconemoides hangzhouensis n. sp. (Nematoda: Criconematidae) from Hangzhou, China
Figure 8: Phylogenetic relationships of Nothocriconemoides hangzhouensis n. sp. with other criconematids species as inferred from Bayesian analysis using the coxI gene sequence dataset with the GTR + I + G model (−lnL=13,473.0592; AIC=27,198.1184; freqA=0.3715; freqC=0.0509; freqG=0.0477; freqT=0.5299; R(a)=0.7544; R(b)=36.5547; R(c)=1.6680; R(d)=51.5187; R(e)=20.3538; R(f)=1.0000; Pinva=0.2510; and Shape=0.3470). Posterior probability more than 70% is given for appropriate clades. Newly obtained sequences are indicated in bold.
Figure 5 in A new rare nematode Nothocriconemoides hangzhouensis n. sp. (Nematoda: Criconematidae) from Hangzhou, China
Figure 5: Phylogenetic relationships of Nothocriconemoides hangzhouensis n. sp. with other criconematids species as inferred from Bayesian analysis using the 18 S rRNA gene sequence dataset with the GTR + I + G model (−lnL=7,315.8130; AIC = 14,859.6260; freqA=0.2371; freqC=0.2413; freqG=0.2833; freqT=0.2384; R(a)=1.5166; R(b)=2.2509; R(c)=09364; R(d)=0.7246; R(e)=6.0997; R(f)=1.0000; Pinva=0.6630; and Shape=0.6070). Posterior probability more than 70% is given for appropriate clades. Newly obtained sequences are indicated in bold.
Figure 6 in A new rare nematode Nothocriconemoides hangzhouensis n. sp. (Nematoda: Criconematidae) from Hangzhou, China
Figure 6: Phylogenetic relationships of Nothocriconemoides hangzhouensis n. sp. with other criconematids species as inferred from Bayesian analysis using the D2-D3 of 28 S rRNA gene sequence dataset with the GTR + I + G model (−lnL=8,382.1334; AIC=16,972.2669; freqA=0.1451; freqC=0.2354; freqG=0.3515; freqT=0.2681; R(a)=0.8404; R(b)=2.5613; R(c)=1.6924; R(d)=0.4616; R(e)=4.7092; R(f)=1.0000; Pinva=0.2730; and Shape=0.8370). Posterior probability more than 70% is given for appropriate clades. Newly obtained sequences are indicated in bold.
Figure 4 in A new rare nematode Nothocriconemoides hangzhouensis n. sp. (Nematoda: Criconematidae) from Hangzhou, China
Figure 4: Scanning electron microscopy of Nothocriconemoides hangzhouensis n. sp. Female. A: Entire body; B-D: En face view; E: Cuticle markings; F-H: tail regions arrows pointing on vulva (v) and anus (a) (Scale bars, A = 100 µm; B, C = 10µ m; D, H = 20 µ m; G-F = 30µ m).
Figure 3 in A new rare nematode Nothocriconemoides hangzhouensis n. sp. (Nematoda: Criconematidae) from Hangzhou, China
Figure 3: Light photomicrographs of Nothocriconemoides hangzhouensis n. sp. Juvenile A: Entire body; B: Cepahlic region; C,D: Esophageal regions: E: Crenation on cuticle; F, G: Tail regions, arrows pointing on anus (a). (Scale bars=A=50 µm, B-I=10µ m).
Figure 4 in Description of Laimaphelenchus sinensis n. sp. (Nematoda: Aphelenchoididae) from declining Chinese pine, Pinus tabuliformis in Beijing, China
Figure 4: Phylogenetic relationships of LaimaphelenChus sinensis n. sp. and aphelenchid nematodes based on D2-D3 expansion segments of 28 S rDNA. The 100001st Bayesian tree inferred from 28 S rDNA under TIM2 + I + G model. AphelenChus avenae (JQ348400) served as the outgroup species. Posterior probability values exceeding 50% are given on appropriate clades.
Figure 1 in A new rare nematode Nothocriconemoides hangzhouensis n. sp. (Nematoda: Criconematidae) from Hangzhou, China
Figure 1: Line drawings of Nothocriconemoides hangzhouensis n. sp. Female A: esophageal region; B: Cepahlic region; C: En face view: D-F: Cuticle markings; G: Tail region under SEM; H: Tail region under LM; I: Cepahlic region of juvenile: J: Crenation on cuticle of juvenile; K: Tail region of juvenile. (Scale bars = A =50µ m, B-I = 10 µ m).
Figure 2 in A new rare nematode Nothocriconemoides hangzhouensis n. sp. (Nematoda: Criconematidae) from Hangzhou, China
Figure 2: Light photomicrographs of Nothocriconemoides hangzhouensis n. sp. Female A: Entire body; B-E: Cepahlic regions; F-H: Esophageal regions, arrow pointing on the excretory pore (exp): I-K: Cuticle markings; L-O: Tail regions, arrows pointing on vulva (v) and anus (a). (Scale bars=A=50 µm, B-I=10µ m).
Figure 2 in Rotylenchus wimbii n. sp. (Nematoda: Hoplolaimidae) associated with finger millet in Kenya
Figure 2: Illustrations of Rotylenchus wimbii n. sp. female. A, B: Anterior part of the body showing lip and neck region; C: En face view; D, E: Lip region; F: Whole body; G to J: Tail region; K: Vulva region. Scales are given in µm.
Figure 2 in Morphological and Molecular Characterization of Punctodera stonei Brzeski, 1998 (Nematoda: Heteroderidae) from Virginia, USA
Figure 2: Phylogenetic relationships within the genus Punctodera: Bayesian 50% majority rule consensus tree from two runs, as inferred from analysis of the D2–D3 of 28S 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.
Figure 1 in Rotylenchus wimbii n. sp. (Nematoda: Hoplolaimidae) associated with finger millet in Kenya
Figure 1-: Light microscopy and scanning electron microscopy images of Rotylenchus wimbii n. sp. female. A to C: En face view; D to I: Anterior part of the body showing lip and neck region; J: Whole female body; K to N: Vulva region; O to V: Tail region.
Figure 6 in Description of a new dagger nematode, Xiphinema barooghii n. sp. (Nematoda: Longidoridae) and additional data on the three known species of the genus from northwest of Iran
Figure 6: (A–E) Xiphinema index Thorne and Allen, 1950, (A) Anterior end; (B) Tubular part of uterus; (C) Vagina; (D) Pars dilatata oviductus; (E) Tail, (F–H) X. pachtaicum (Tulaganov, 1938) Kirjanova, 1951, (F) Anterior end; (G) Anterior genital branch; (H) Tail, (I–N) X. vuittenezi Luc, Lima, Weischer and Flegg, 1964, (I) Anterior end; (J, L) Uterine differentiation spines; (K) Vagina; (M, N) Tail. (Scale bars =10 μm).
Figure 5 in Description of a new dagger nematode, Xiphinema barooghii n. sp. (Nematoda: Longidoridae) and additional data on the three known species of the genus from northwest of Iran
Figure 5: Bayesian tree inferred under the GTR + I + G model from 28S rDNA D2–D3 expansion domains of X. barooghii n. sp. and X. index (−lnL = 9,085.8555; AIC = 18,191.7109; freqA = 0.2402; freqC = 0.2341; freqG = 0.2885; freqT = 0.2373; R (a) = 1.0503; R (b) = 2.8325; R (c) = 2.6784; R (d) = 0.5047; R (e) = 4.0878; R (f) = 1.0000). Posterior probabilities are given for appropriate clades. Newly obtained sequences are indicated by bold letters.
Figure 1 in Description of a new dagger nematode, Xiphinema barooghii n. sp. (Nematoda: Longidoridae) and additional data on the three known species of the genus from northwest of Iran
Figure 1: Xiphinema barooghii n. sp. (A) Amphidial pouch; (B) Entire body; (C) Neck region; (D) Female tail; (E) Anterior end; (F) Posterior genital branch; (G–J) Tail of juveniles from J1–J4, respectively.
Figure 3 in Description of a new dagger nematode, Xiphinema barooghii n. sp. (Nematoda: Longidoridae) and additional data on the three known species of the genus from northwest of Iran
Figure 3: Juvenile stages of Xiphinema barooghii n. sp. Anterior region and tail shape of (A, B) first; (C, D) second; (E, F) third and (G, H) fourth juvenile stages, respectively (Scale bars =10 μm).
Figure 2 in Description of a new dagger nematode, Xiphinema barooghii n. sp. (Nematoda: Longidoridae) and additional data on the three known species of the genus from northwest of Iran
Figure 2: Xiphinema barooghii n. sp. Female (A, B) anterior end; (C, G) uterine differentiation spines; (D) entire body; (E) reproductive system; (F) vagina; (H) tail; (I) caudal pores in lateral optical view; (J) amphidial pouch; (K) pharyngeal expansion. (Scale bars: A–K = 10 μm, D = 70 μm).
Figure 4 in Description of a new dagger nematode, Xiphinema barooghii n. sp. (Nematoda: Longidoridae) and additional data on the three known species of the genus from northwest of Iran
Figure 4: Xiphinema barooghii n. sp. Graph of correlation of functional and replacement odontostyle to body length in all developmental stages from Jl to mature females.
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.
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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)
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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.