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Fig. 6. Female P in Protostrongylus caprae Zdzitowiecki et Boev, 1971 (Nematoda: Protostrongylidae) - First record in Alpine ibex (Capra ibex Linnaeus, 1758) from Europe
Fig. 6. Female P. caprae from an Alpine ibex from Austria: 1 — anus, 2 —provagina, 3 — vulva.
Fig. 1 in The first finding of Dictyocaulus cervi and Dictyocaulus skrjabini (Nematoda) in feral fallow deer (Dama dama) in Australia
Fig. 1. Map of collection locations for feral deer examined in this study.
Table 3 in New species and new records of camallanid nematodes (Nematoda, Camallanidae) from marine fishes and sea snakes in New Caledonia
<p><b>Table 3.</b> Comparison of measurements of <i>Camallanus carangis</i> four-stage larvae from fish and reptilian hosts in New Caledonia.</p><table><tbody><tr><th>Host <i>Parupeneus</i></th><th><i>Chirocentrus</i></th><th><i>Laticauda</i></th></tr></tbody><tbody><tr><th></th><td><i>indicus</i></td><td><i>dorab</i></td><td><i>saintgironsi *</i></td></tr><tr><th>No. of specimens</th><td>1</td><td>1</td><td>1</td></tr><tr><th>Body length (in mm)</th><td>3.13</td><td>4.12</td><td>1.31</td></tr><tr><th>Body width</th><td>136</td><td>109</td><td>122</td></tr><tr><th>Buccal capsule – length</th><td>84</td><td>105</td><td>102</td></tr><tr><th>Buccal capsule – width</th><td>69</td><td>69</td><td>90</td></tr><tr><th>No. of ridges</th><td>17</td><td>?</td><td>18</td></tr><tr><th>Basal ring – length</th><td>12</td><td>21</td><td>24</td></tr><tr><th>Basal ring – width</th><td>51</td><td>51</td><td>54</td></tr><tr><th>Length of prongs</th><td>78</td><td>123</td><td>117</td></tr><tr><th>Oesoph. cup – length</th><td>18</td><td>24</td><td>18</td></tr><tr><th>Oesoph. cup – width</th><td>21</td><td>21</td><td>21</td></tr><tr><th>Musc. oesoph. – length</th><td>435</td><td>571</td><td>517</td></tr><tr><th>Musc. oesoph. – width</th><td>63</td><td>60</td><td>45</td></tr><tr><th>Gland. oesoph. – length</th><td>394</td><td>490</td><td>435</td></tr><tr><th>Gland. oesoph. – width</th><td>72</td><td>60</td><td>45</td></tr><tr><th>Musc./gland. oesoph.</th><td>1:091</td><td>1:0.86</td><td>1:0.84</td></tr><tr><th>length ratio</th><td></td><td></td><td></td></tr><tr><th>% of buc. c. and</th><td>2</td><td>28</td><td>81</td></tr><tr><th>oesoph. of body</th><td></td><td></td><td></td></tr><tr><th>Tail</th><td>72</td><td>147</td><td>54</td></tr></tbody></table><p><sup>*</sup> Sea-snake (Reptilia).</p>
Table 2 in New species and new records of camallanid nematodes (Nematoda, Camallanidae) from marine fishes and sea snakes in New Caledonia
<p><b>Table 2.</b> Comparison of measurements of <i>Camallanus carangis</i> females from marine fishes in New Caledonia.</p><table><tbody><tr><th>Host</th><th><i>Atule</i></th><th><i>Carangoides</i></th><th><i>Selar</i></th><th><i>Parupeneus</i></th><th><i>Pristipomoides</i></th><th><i>Epinephelus</i></th></tr></tbody><tbody><tr><th></th><td><i>mate</i></td><td><i>dinema</i></td><td><i>crumenophthalmus</i></td><td><i>cyclostomus</i></td><td><i>filamentosus</i></td><td><i>retouti</i></td></tr><tr><th>No. of specimens 1 (grav.)</th><td>2 (subgr.)</td><td>3 (gr., subgr.)</td><td>2 (subgr.)</td><td>1 (subgr.)</td><td>1 (subgr.)</td></tr><tr><th>Body length (in mm)</th><td>14.93</td><td>4.75 –7.00</td><td>14.63–17.00</td><td>10.23–11.13</td><td>14.89</td><td>10.95</td></tr><tr><th>Body width</th><td>340</td><td>163–245</td><td>381–517</td><td>340–408</td><td>313</td><td>354</td></tr><tr><th>Buccal capsule – length</th><td>195</td><td>159–180</td><td>186–225</td><td>159</td><td>150</td><td>183</td></tr><tr><th>Buccal capsule – width</th><td>198</td><td>144–180</td><td>204–233</td><td>144</td><td>159</td><td>195</td></tr><tr><th>No. of ridges</th><td>32</td><td>37–40</td><td>35–50</td><td>?</td><td>32</td><td>44</td></tr><tr><th>Basal ring – length</th><td>30</td><td>27</td><td>24–36</td><td>21–24</td><td>24</td><td>30</td></tr><tr><th>Basal ring – width</th><td>111</td><td>96</td><td>108–117</td><td>96–99</td><td>90</td><td>108</td></tr><tr><th>Length of tridents</th><td>141</td><td>135</td><td>195–240</td><td>105–195</td><td>141</td><td>153</td></tr><tr><th>Oesoph. cup – length</th><td>27</td><td>24–30</td><td>30–39</td><td>33</td><td>15</td><td>36</td></tr><tr><th>Oesoph. cup – width</th><td>36</td><td>30–36</td><td>39–45</td><td>36</td><td>33</td><td>30</td></tr><tr><th>Musc. oesoph. – length</th><td>1550</td><td>721–1047</td><td>1333–1850</td><td>816–979</td><td>911</td><td>1469</td></tr><tr><th>Musc. oesoph. – width</th><td>136</td><td>90</td><td>123–177</td><td>122–136</td><td>163</td><td>122</td></tr><tr><th>Gland. oesoph. – length</th><td>1333</td><td>653–911</td><td>1156–1659</td><td>775–925</td><td>993</td><td>1156</td></tr><tr><th>Gland. oesoph. – width</th><td>136</td><td>96–99</td><td>114–190</td><td>122–163</td><td>163</td><td>136</td></tr><tr><th>Musc./gland. oesoph.</th><td>1:0.86</td><td>1:0.87–0.91</td><td>1:0.87–0.98</td><td>1:0.94–0.95</td><td>1:1.09</td><td>1:0.79</td></tr><tr><th>length ratio</th></tr><tr><th>% of buc. c. and oesoph.</th><td>21</td><td>22–40</td><td>18–25</td><td>17–19</td><td>14</td><td>26</td></tr><tr><th>of body</th></tr><tr><th>Excretory pore</th><td>1401</td><td>707–911</td><td>1591</td><td>?</td><td>?</td><td>1224</td></tr><tr><th>Vulva from ant. end (in</th><td>7.51</td><td>2.56–3.93</td><td>7.13–8.80</td><td>4.92</td><td>7.00</td><td>5.74</td></tr><tr><th>mm)</th></tr><tr><th>% of vulva of body</th><td>50</td><td>54–56</td><td>49–55</td><td>48</td><td>47</td><td>52</td></tr><tr><th>Tail</th><td>272</td><td>90–136</td><td>225</td><td>144–147</td><td>177</td><td>190</td></tr></tbody></table>
Table 1 in New species and new records of camallanid nematodes (Nematoda, Camallanidae) from marine fishes and sea snakes in New Caledonia
<p><b>Table 1.</b> Comparison of measurements of <i>Camallanus carangis</i> males from marine fishes in New Caledonia.</p><table><tbody><tr><th>Host</th><th><i>Atule mate</i></th><th><i>Carangoides fulvoguttatus</i></th><th><i>Cephalopholis sonnerati</i></th><th><i>Epinephelus retouti</i></th></tr></tbody><tbody><tr><th>No. of specimens</th><td>2</td><td>1</td><td>3</td><td>1</td></tr><tr><th>Body length (in mm)</th><td>12.17–13.67</td><td>6.90</td><td>9.93–11.32</td><td>frag. 5.40</td></tr><tr><th>Body width</th><td>299–354</td><td>218</td><td>258–326</td><td>258</td></tr><tr><th>Buccal capsule – length</th><td>165–189</td><td>162</td><td>183–186</td><td>159</td></tr><tr><th>Buccal capsule – width</th><td>159–189</td><td>156</td><td>156–183</td><td>165</td></tr><tr><th>No. of ridges</th><td>33–35</td><td>38</td><td>34–35</td><td>40</td></tr><tr><th>Basal ring – length</th><td>21–24</td><td>27</td><td>27–33</td><td>27</td></tr><tr><th>Basal ring – width</th><td>90–105</td><td>90</td><td>96–102</td><td>93</td></tr><tr><th>Length of tridents</th><td>150</td><td>150</td><td>171–219</td><td>153</td></tr><tr><th>Oesoph. cup – length</th><td>21–30</td><td>30</td><td>30–36</td><td>36</td></tr><tr><th>Oesoph. cup – width</th><td>24–33</td><td>39</td><td>36–39</td><td>30</td></tr><tr><th>Musc. oesoph. – length</th><td>1183–1414</td><td>1020</td><td>1333–1170</td><td>1102</td></tr><tr><th>Musc. oesoph. – width</th><td>122–136</td><td>81</td><td>122–136</td><td>84</td></tr><tr><th>Gland. oesoph. – length</th><td>1156–1333</td><td>857</td><td>1034–1238</td><td>1673</td></tr><tr><th>Gland. oesoph. – width</th><td>136</td><td>96</td><td>122–136</td><td>90</td></tr><tr><th>Musc./gland. oesoph. length ratio</th><td>1:0.94–0.98</td><td>1:084</td><td>1:0.88–0.93</td><td>1:0.79</td></tr><tr><th>% of buc. c. and oesoph. of body</th><td>21</td><td>30</td><td>23–24</td><td>–</td></tr><tr><th>Excretory pore</th><td>1047–1387</td><td>?</td><td>1115–1251</td><td>?</td></tr><tr><th>Right spicule</th><td>306–309</td><td>300</td><td>294–312</td><td>–</td></tr><tr><th>Tail</th><td>75–81</td><td>102</td><td>84–117</td><td>–</td></tr></tbody></table>
Fig. 2 in Icosiella Neglecta (Nematoda, Onchocercidae) In Ukraine: Occurrence, Hosts, Morphological And Molecular Characterisation
Fig. 2. Icosiella neglecta in host leg (A) and throat (B) muscles.
Fig. 1 in Icosiella Neglecta (Nematoda, Onchocercidae) In Ukraine: Occurrence, Hosts, Morphological And Molecular Characterisation
Fig. 1. Studied localities in Ukraine. Numbers correspond to those in table 1.
Figure 1 in A new species of Maldivea Gerlach, 1962 (Nematoda, Oxystominidae) from Felidhoo atoll (Maldives, Indian Ocean) and an emended diagnosis of the sub-family and genus
Figure 1. Type localities of Maldivea xarifae and M. complexa n. sp.
Figure 2 in A new species of Maldivea Gerlach, 1962 (Nematoda, Oxystominidae) from Felidhoo atoll (Maldives, Indian Ocean) and an emended diagnosis of the sub-family and genus
Figure 2. Drawing of the total body of the male of Maldivea complexa n. sp. Scale bar: 100 µm.
Fig. 1 in On Some Species of Enchodelus Thorne, 1939 from India (Nematoda: Dorylaimidae)
Fig. 1. Enchodelus macrodorus (De Man, 1880): female, head end.
Data from: Phylogenomic insights into the evolution and origin of nematoda
Open the record for dataset details and reuse information.
The first phylogenetic reconstruction of Nippostrongylinae (Nematoda: Heligmonellidae) reveals 3 new genera, the polyphyletic nature of Carolinensis and Vexillata, and identifies 5 clades with varying associations with mammals
Open the record for dataset details and reuse information.
FIGURE 4 in A new species of Aoruroides Travassos & Kloss, 1958 (Nematoda: Oxyuridomorpha Thelastomatidae) parasite of the wood-burrowing cockroach Panesthia angustipennis spadica (Shiraki, 1906) (Blattodea: Blaberidae: Panesthiinae) from Japan with comments on the validity of the genus Aoruroides
FIGURE 4. Maximum likelihood (ML) tree inferred from the D2-D3 LSU rDNA for several species of the family Thelastomatidae (Nematoda: Oxyuridomorpha: Thelastomatoidea). Hystrignathus sp. (Hystrignathidae), Cameronia multiovata (Thelastomatidae) and three species of Travassosinema (Travassosinematidae) were used as outgroup taxa (in red). Values at the nodes correspond to bootstrap resampling (≥70)/posterior probability (≥0.90). Newly obtained sequences in bold.
FIGURE 3. Aoruroides chubudaigaku n in A new species of Aoruroides Travassos & Kloss, 1958 (Nematoda: Oxyuridomorpha Thelastomatidae) parasite of the wood-burrowing cockroach Panesthia angustipennis spadica (Shiraki, 1906) (Blattodea: Blaberidae: Panesthiinae) from Japan with comments on the validity of the genus Aoruroides
FIGURE 3. Aoruroides chubudaigaku n. sp. (Nematoda: Oxyuridomorpha: Thelastomatidae). SEM images. Female. A. Cephalic end. B. Cephalic end, en face view. C. Vulva, ventral view. D. Anus, ventro-lateral view. Male. E. Cephalic end. F. Cephalic end, en face view. G. Cloacal region, ventro-lateral view. H. Cloacal region, ventral view (detail of the distal end of the post-cloacal appendage at the inferior left corner of the picture). Scale bars: A, C, D. 20 µm. B, G, H. 10 µm. E, F. 5 µm. Detail of the post-cloacal appendage. 2 µm.
FIGURE 1. Aoruroides chubudaigaku n in A new species of Aoruroides Travassos & Kloss, 1958 (Nematoda: Oxyuridomorpha Thelastomatidae) parasite of the wood-burrowing cockroach Panesthia angustipennis spadica (Shiraki, 1906) (Blattodea: Blaberidae: Panesthiinae) from Japan with comments on the validity of the genus Aoruroides
FIGURE 1. Aoruroides chubudaigaku n. sp. (Nematoda: Oxyuridomorpha: Thelastomatidae). Female. A. Oesophageal region, lateral view. B. Tail, lateral view. C. Cephalic end, en face view (reconstructed from SEM images). D. Cephalic end (reconstruct- ed from SEM images). E. Vagina vera and vagina uterina, lateral view. F. Genital tract, lateral view. G. Habitus, lateral view.
FIGURES 9–18 in First description of male worms of Enterobius Colobenterobius serratus Nematoda: Oxyuridae , the pinworm parasite of proboscis monkeys
FIGURES 9–18. Esophageal region of female pinworms. 9. Enterobius (Colobenterobius) serratus; 10. E. (C.) emodensis; 11. E. (C.) pygatrichus; 12. E. (Enterobius) macaci; 13. E. (E.) vermicularis; 14. E. (E.) anthropopitheci; 15. Trypanoxyuris (Buckleyenterobius) atelis; 16. T. (Trypanoxyuris) microon; 17. Lemuricola (Protenterobius) nycticebi; 18. L. (Madoxyuris) vauceli. Arrow indicates junction between light and dark portions. Scale bar: 100 µm.
FIGURES 19–22 in First description of male worms of Enterobius Colobenterobius serratus Nematoda: Oxyuridae , the pinworm parasite of proboscis monkeys
FIGURES 19–22. Cross section near caudal extremity of male (a) and enlarged view of the boxed part (b) showing spicular pouch. 19. Enterobius (Colobenterobius) serratus; 20. E. (C.) emodensis; 21. E. (Enterobius) vermicularis; 22. Lemuricola (Protenterobius) nycticebi. Thick arrows indicate dorso-ventral height of spicular pouch; thin arrows indicate dorso-ventral height of spicule.
FIGURES 1–8 in First description of male worms of Enterobius Colobenterobius serratus Nematoda: Oxyuridae , the pinworm parasite of proboscis monkeys
FIGURES 1–8. Male adult of Enterobius (Colobenterobius) serratus Hasegawa et al., 2003, collected from the feces of Nasalis larvatus in Sabah, Malaysia. 1. Entire worm, left lateral view; 2–4. Cephalic extremity, left lateral view (2), optical frontal section (3) and apical view (4); 5. Lateral ala in cross section through midbody; 6. Caudal extremity, left lateral view; 7. Spicular pouch, cross section; 8. Caudal papillae arrangement, ventral view. Abbreviations used: am. amphidial pore; an. anus; ce. cephalic expansion; co. corpus (of esophagus); cp. cephalic papilla; dl. dorsal lip; eb. esophageal bulb; ep. excretory pore; in. intestine; is. isthmus (of esophagus); la. lateral ala; mo. mouth; nr. nerve ring; pd. phasmidial duct; p1–p4. caudal papillae arrangement; ph. pharynx; sl. slot; sp. spicule; ss. specific structure (teeth) of pharynx; sv. seminal vesicle; svl. subventral lip; t. testis; vd. vas deferens.
FIGURE 1 in Wieseria bicepes sp. nov. (Nematoda: Oxystominidae) from the South China Sea
FIGURE 1. Wieseria bicepes sp. nov. (A) anterior end of male, showing labial and cephalic setae, amphideal fovea; (B) anterior end of juvenile; (C) pharyngeal region of male; (D) spicule and precloacal spine; (E) posterior end of male, showing spicule, precloacal spine and bifurcate tail tip; (F) tail end of juvenile, showing caudal glands and bifurcate tail tip.
FIGURE 5 in Three new species of Cloacininae (Nematoda: Strongyloidea) parasitic in Dorcopsis muelleri (Schlegel, 1866) from Papua and Salawati Island, Indonesia
FIGURE 5. Cervonemela kaimanaensis sp.nov. A. Anterior end, lateral view; B. Cephalic extremity, lateral view; C. Submedian cephalic papilla, lateral view; D. Tips of two spicules, lateral view; E. Bursa, apical view; F. Gubernaculum, ventral view; G. Vagina and ovejector, lateral view; H. Female tail, lateral view; Scale bars: A: 100 µm, B: 25 µm, C: 1 µm, D, E, H: 100 µm, F: 5 µm.
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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.