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89 results for “Longidorus”
Figure 2 in Morphological and Molecular Characterization of Paralongidorus sali Siddiqi, Hooper, and Khan, 1963 with a Description of the First-Stage Juvenile and Male of Longidorus jonesi Siddiqi, 1962 from China
Figure 2: Light micrographs of ParalONgidOrUS Sali (Siddiqi et al., 1963). A–D, lip region of 1st, 2nd, and 3rd stage juveniles and female; E–H, Tail region of 1st, 2nd, and 3rd stage juveniles and female (Scale bars: A–H = 10 μm).
Figure 1 in Morphological and Molecular Characterization of Paralongidorus sali Siddiqi, Hooper, and Khan, 1963 with a Description of the First-Stage Juvenile and Male of Longidorus jonesi Siddiqi, 1962 from China
Figure 1: Light micrographs of ParalONgidOrUS Sali (Siddiqi et al., 1963). Female: A, Pharynx; B–D, Lip region arrow showing amphid; E, Gonad; F, Tail region arrow showing position of anus G, Tail region arrows showing position of caudal pores; H, Ventral view of vulva; I, Vulval region (Scale bars: A = 50 μm; B–D= 10 μm; E= 50 μm; F–I= 10 μm).
Figure 11 in Morphological and Molecular Characterization of Paralongidorus sali Siddiqi, Hooper, and Khan, 1963 with a Description of the First-Stage Juvenile and Male of Longidorus jonesi Siddiqi, 1962 from China
Figure 11: Phylogenetic relationships within LONgidOrUS and ParalONgidOrUS. Bayesian 50% majority rule consensus tree as inferred from 18S rRNA gene sequence alignment under a transitional of invariable sites model with invariable sites and a gamma-shaped distribution (TIM2 + I + G: – lnL= 6866.9821; AIC = 14129.9643; freqA = 0.2626; freqC = 0.2109; freqG = 0.2668; freqT = 0.2597; R(a) = 1.8892; R(b) = 3.9662; R(c) = 1.8892; R(d) = 1.0000; R(e) = 7.1009; R(f) = 1.0000; Pinva = 0.7060; and Shape = 0.6020). Posterior probabilities greater than 0.70 are given for appropriate clades. Newly obtained sequences in this study are shown in bold. Scale bar = expected changes per site.
Figure 7 in Morphological and Molecular Characterization of Paralongidorus sali Siddiqi, Hooper, and Khan, 1963 with a Description of the First-Stage Juvenile and Male of Longidorus jonesi Siddiqi, 1962 from China
Figure 7: Light micrographs of LONgidOrUS JONeSi (Siddiqi, 1962). A–D, lip region of 1st, 2nd, 3rd, and 4th stage juveniles; E–H, Tail region of 1st, 2nd, 3rd, and 4th stage juveniles (Scale bars: A–H = 10 μm).
Figure 5 in Morphological and Molecular Characterization of Paralongidorus sali Siddiqi, Hooper, and Khan, 1963 with a Description of the First-Stage Juvenile and Male of Longidorus jonesi Siddiqi, 1962 from China
Figure 5: Light micrographs of LONgidOrUS JONeSi (Siddiqi, 1962). Female: A, Pharynx; B–E, Lip regions; F, Gonad; G–H, Pharyngeal bulb; I, Entire female body; J–K, Vulval regions; L, ventral view of tail; M–O, Female tails (Scale bars: A = 50 μm; B–E, G–H, J–O = 10 μm; F = 20 μm; I = 500 μm) am = amphid; bp = body pores; v = vulva; svn = subventrolateral nuclei; dn = dorsal nuclei; a = anus).
Figure 4 in Morphological and Molecular Characterization of Paralongidorus sali Siddiqi, Hooper, and Khan, 1963 with a Description of the First-Stage Juvenile and Male of Longidorus jonesi Siddiqi, 1962 from China
Figure 4: Relationship of body length to length of functional and replacement odontostyle (= Odontostyle and • = replACement ODOntOStyle); length in three developmental stages and mature females of ParalONgidOrUS Sali.
FIGURE 1 in Past and present distribution and hosts of Longidorus (Nematoda: Dorylaimida) in mainland China
FIGURE 1. The geographical distribution of Longidorus species occurring in China. —location of Longidorus samples (samples from different hosts were frequently obtained from the same location).
FIGURE 4 in Past and present distribution and hosts of Longidorus (Nematoda: Dorylaimida) in mainland China
FIGURE 4. Photomicrographs of Longidorus. A–E) female anterior region, L. jonesi, L litchii, L. macromucronatus, L. fursti, L. camelliae, respectively. F–J) female posterior region, L. jonesi, L.litchii, L. macromucronatus, L. fursti, L. camelliae, respectively.
FIGURE 3 in Past and present distribution and hosts of Longidorus (Nematoda: Dorylaimida) in mainland China
FIGURE 3. Photomicrographs of Longidorus. A–D) female anterior region, L. hangzhouensis, L. henanus, L. fangi, L. pisi, respectively. F–I) female posterior region, L. hangzhouensis, L. henanus, L. fangi, L. pisi, respectively. E: male anterior region of L. pisi. J: male posterior region of L. pisi.
FIGURE 2 in Past and present distribution and hosts of Longidorus (Nematoda: Dorylaimida) in mainland China
FIGURE 2. Occurrence and distribution of Longidorus henanus and Longidorus litchii in China.): L. henanus): L. litchii.
Supplementary material 3 from: Gutiérrez-Gutiérrez C, Teixeira Santos M, Inácio ML, Eisenback JD, Mota M (2020) Description of Longidorus bordonensis sp. nov. from Portugal, with systematics and molecular phylogeny of the genus (Nematoda, Longidoridae). Zoosystematics and Evolution 96(1): 175-193. https://doi.org/10.3897/zse.96.49022
Table S1
Supplementary material 2 from: Gutiérrez-Gutiérrez C, Teixeira Santos M, Inácio ML, Eisenback JD, Mota M (2020) Description of Longidorus bordonensis sp. nov. from Portugal, with systematics and molecular phylogeny of the genus (Nematoda, Longidoridae). Zoosystematics and Evolution 96(1): 175-193. https://doi.org/10.3897/zse.96.49022
Figure S2
Supplementary material 4 from: Gutiérrez-Gutiérrez C, Teixeira Santos M, Inácio ML, Eisenback JD, Mota M (2020) Description of Longidorus bordonensis sp. nov. from Portugal, with systematics and molecular phylogeny of the genus (Nematoda, Longidoridae). Zoosystematics and Evolution 96(1): 175-193. https://doi.org/10.3897/zse.96.49022
Table S2
Supplementary material 1 from: Gutiérrez-Gutiérrez C, Teixeira Santos M, Inácio ML, Eisenback JD, Mota M (2020) Description of Longidorus bordonensis sp. nov. from Portugal, with systematics and molecular phylogeny of the genus (Nematoda, Longidoridae). Zoosystematics and Evolution 96(1): 175-193. https://doi.org/10.3897/zse.96.49022
Figure S1
Figure 5 from: Gutiérrez-Gutiérrez C, Teixeira Santos M, Inácio ML, Eisenback JD, Mota M (2020) Description of Longidorus bordonensis sp. nov. from Portugal, with systematics and molecular phylogeny of the genus (Nematoda, Longidoridae). Zoosystematics and Evolution 96(1): 175-193. https://doi.org/10.3897/zse.96.49022
Figure 5 Phylogenetic relationships of Longidorus bordonensis sp. nov., L. wicuolea Archidona-Yuste, Navas-Cortés, Cantalapiedra-Navarrete, Palomares-Rius & Castillo, L. vinearum Bravo & Roca and L. vineacola Sturhan & Weischer, 1964 within the genus Longidorus. Bayesian 50% majority rule consensus trees as inferred from ITS1 rRNA sequences alignments under the SYM model. Posterior probabilities more than 70% are given for appropriate clades. Newly obtained sequences in this study are coloured in green. Scale bar: expected changes per site.
Figure 4 from: Gutiérrez-Gutiérrez C, Teixeira Santos M, Inácio ML, Eisenback JD, Mota M (2020) Description of Longidorus bordonensis sp. nov. from Portugal, with systematics and molecular phylogeny of the genus (Nematoda, Longidoridae). Zoosystematics and Evolution 96(1): 175-193. https://doi.org/10.3897/zse.96.49022
Figure 4 Phylogenetic relationships of Longidorus bordonensis sp. nov. and L. vineacola Sturhan & Weischer, 1964 within the genera Longidorus and Paralongidorus. Bayesian 50% majority rule consensus trees as inferred from 18S rRNA sequences alignments under the SYM model. Posterior probabilities more than 70% are given for appropriate clades. Newly obtained sequences in this study are coloured in light blue. Scale bar: expected changes per site.
Supplementary material 5 from: Gutiérrez-Gutiérrez C, Teixeira Santos M, Inácio ML, Eisenback JD, Mota M (2020) Description of Longidorus bordonensis sp. nov. from Portugal, with systematics and molecular phylogeny of the genus (Nematoda, Longidoridae). Zoosystematics and Evolution 96(1): 175-193. https://doi.org/10.3897/zse.96.49022
Table S3
Figure 3 from: Gutiérrez-Gutiérrez C, Teixeira Santos M, Inácio ML, Eisenback JD, Mota M (2020) Description of Longidorus bordonensis sp. nov. from Portugal, with systematics and molecular phylogeny of the genus (Nematoda, Longidoridae). Zoosystematics and Evolution 96(1): 175-193. https://doi.org/10.3897/zse.96.49022
Figure 3 Phylogenetic relationships of Longidorus bordonensis sp. nov., L. wicuolea Archidona-Yuste, Navas-Cortés, Cantalapiedra-Navarrete, Palomares-Rius & Castillo, L. lusitanicus Macara, 1986, L. vinearum Bravo & Roca and L. vineacola Sturhan & Weischer, 1964 within the genus Longidorus. Bayesian 50% majority rule consensus trees as inferred from D2–D3 expansion segments of 28S rRNA sequences alignments under the SYM model. Posterior probabilities more than 70% are given for appropriate clades. Newly obtained sequences in this study are coloured in purple. Scale bar: expected changes per site.
Figure 1 from: Gutiérrez-Gutiérrez C, Teixeira Santos M, Inácio ML, Eisenback JD, Mota M (2020) Description of Longidorus bordonensis sp. nov. from Portugal, with systematics and molecular phylogeny of the genus (Nematoda, Longidoridae). Zoosystematics and Evolution 96(1): 175-193. https://doi.org/10.3897/zse.96.49022
Figure 1 Line drawings of Longidorus bordonensis sp. nov. paratypes from the rhizosphere of grass (unknown species) at São Pedro do Sul, Viseu district, northern Portugal (1–7). 1. Female anterior end. 2. Female lip region. 3. Female tail region. 4. Spicule and lateral guiding piece of gubernaculum. 5. Vulva region. 6. Male tail region. 7. Detail of basal pharyngeal bulb. Scale bars: 23 μm (1–3); 24 μm (4, 6); 29 μm (5); 15 μm (7).
Supplementary material 6 from: Gutiérrez-Gutiérrez C, Teixeira Santos M, Inácio ML, Eisenback JD, Mota M (2020) Description of Longidorus bordonensis sp. nov. from Portugal, with systematics and molecular phylogeny of the genus (Nematoda, Longidoridae). Zoosystematics and Evolution 96(1): 175-193. https://doi.org/10.3897/zse.96.49022
Table S4
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