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Figure 2 in Variation in leukocyte indices and immunoglobulin levels according to host density, sex, flea burden and tularemia prevalence in the common vole Microtus arvalis
Figure 2: Relationship between the neutrophil-to-lymphocyte (N:L) ratio and vole density index according to sex. Vole density was estimated as the number of captured voles/100 traps/24 h. Grey shaded areas show the 95 % confidence intervals of the predicted curves.
Figure 1 in Variation in leukocyte indices and immunoglobulin levels according to host density, sex, flea burden and tularemia prevalence in the common vole Microtus arvalis
Figure 1: Relationship between the a) neutrophil-to-lymphocyte (N:L) ratio and immunoglobulin (Ig) levels according to vole sex, and between the b) proportion of eosinophils and Ig levels. Grey shaded areas show the 95 % confidence intervals of the predicted curves.
TABLE 1. Host species and morphological measurements for the 13 in A new species of the fish louse genus Dipteropeltis Calman, 1912 (Crustacea: Branchiura) from Peru
<p><b>TABLE 1.</b> Host species and morphological measurements for the 13 specimens collected. Groups correspond to <i>Dipteropeltis longicaudatus</i> <b>sp. nov.</b> adults (I) and juveniles (II), as well as <i>Dipteropeltis hirundo</i> (III). Specimen I.2 is the holotype (MUSM 5128). Specimen II.1 was found on host <i>Brycon amazonicus</i>; no measurements were taken before its loss. Gravid specimens denoted with asterisk (*). Measurements and ratios are based on Neethling <i>et al</i>. 2014: abdomen length (AL), abdomen split length (ASL), carapace split length (CSL), distance from head to abdominal lobe end (HA), distance from head to carapace lobe end (HC), and sucker diameter (SD). Units are in millimeters (mm).</p><table><tbody><tr><th><b>Specimen ID</b></th><th><b>Host species</b></th><th><b>AL</b></th><th><b>ASL</b></th><th><b>CSL</b></th><th><b>HA</b></th><th><b>HC</b></th><th><b>SD</b></th><th><b>HC/HA</b></th><th><b>HA/HC</b></th><th><b>CSL/HC</b></th><th><b>ASL/AL</b></th><th><b>AL/HA</b></th><th><b>AL/HC</b></th><th><b>SD/HA</b></th><th><b>SD/HC</b></th></tr></tbody><tbody><tr><th><b>I.1*</b></th><td><i>Triportheus albus</i></td><td>11.3</td><td>10.4</td><td>6.3</td><td>19.0</td><td>9.5</td><td>1.0</td><td>0.50</td><td>2.00</td><td>0.66</td><td>0.92</td><td>0.59</td><td>1.19</td><td>0.05</td><td>0.11</td></tr><tr><th><b>I.2*</b></th><td><i>Triportheus albus</i></td><td>11.0</td><td>9.5</td><td>7.0</td><td>17.5</td><td>10.0</td><td>1.0</td><td>0.57</td><td>1.75</td><td>0.70</td><td>0.86</td><td>0.63</td><td>1.10</td><td>0.06</td><td>0.10</td></tr><tr><th><b>I.3</b></th><td><i>Brycon amazonicus</i></td><td>8.0</td><td>7.0</td><td>6.5</td><td>14.0</td><td>8.5</td><td>1.0</td><td>0.61</td><td>1.65</td><td>0.76</td><td>0.88</td><td>0.57</td><td>0.94</td><td>0.07</td><td>0.12</td></tr><tr><th><b>I.4*</b></th><td><i>Triportheus albus</i></td><td>22.0</td><td>20.5</td><td>12.5</td><td>31.5</td><td>16.0</td><td>1.0</td><td>0.51</td><td>1.97</td><td>0.78</td><td>0.93</td><td>0.70</td><td>1.38</td><td>0.03</td><td>0.06</td></tr><tr><th><b>I.5</b></th><td><i>Brycon amazonicus</i></td><td>12.5</td><td>10.5</td><td>5.5</td><td>19.5</td><td>7.5</td><td>0.8</td><td>0.38</td><td>2.60</td><td>0.73</td><td>0.84</td><td>0.64</td><td>1.67</td><td>0.04</td><td>0.10</td></tr><tr><th><b>I.6</b></th><td><i>Brycon amazonicus</i></td><td>7.0</td><td>6.5</td><td>5.0</td><td>11.0</td><td>7.5</td><td>0.8</td><td>0.68</td><td>1.47</td><td>0.67</td><td>0.93</td><td>0.64</td><td>0.93</td><td>0.07</td><td>0.10</td></tr><tr><th><b>I.7</b></th><td><i>Triportheus albus</i></td><td>7.0</td><td>5.5</td><td>5.0</td><td>13.0</td><td>7.5</td><td>0.8</td><td>0.58</td><td>1.73</td><td>0.67</td><td>0.79</td><td>0.54</td><td>0.93</td><td>0.06</td><td>0.10</td></tr><tr><th><b>II.2</b></th><td><i>Brycon amazonicus</i></td><td>1.5</td><td>1.3</td><td>1.5</td><td>4.5</td><td>3.0</td><td>0.5</td><td>0.67</td><td>1.50</td><td>0.50</td><td>0.83</td><td>0.33</td><td>0.50</td><td>0.11</td><td>0.17</td></tr><tr><th><b>II.3</b></th><td><i>Brycon amazonicus</i></td><td>1.5</td><td>1.0</td><td>2.0</td><td>5.0</td><td>3.5</td><td>0.5</td><td>0.70</td><td>1.43</td><td>0.57</td><td>0.67</td><td>0.30</td><td>0.43</td><td>0.10</td><td>0.14</td></tr><tr><th><b>II.4</b></th><td><i>Brycon amazonicus</i></td><td>0.8</td><td>0.5</td><td>0.8</td><td>3.0</td><td>2.0</td><td>0.3</td><td>0.67</td><td>1.50</td><td>0.38</td><td>0.67</td><td>0.25</td><td>0.38</td><td>0.08</td><td>0.13</td></tr><tr><th><b>II.5</b></th><td><i>Brycon amazonicus</i></td><td>1.3</td><td>1.0</td><td>2.0</td><td>4.5</td><td>3.3</td><td>0.5</td><td>0.72</td><td>1.38</td><td>0.62</td><td>0.80</td><td>0.28</td><td>0.38</td><td>0.11</td><td>0.15</td></tr><tr><th><b>II.6</b></th><td><i>Triportheus albus</i></td><td>1.0</td><td>0.8</td><td>1.0</td><td>3.5</td><td>2.5</td><td>0.5</td><td>0.71</td><td>1.40</td><td>0.40</td><td>0.75</td><td>0.29</td><td>0.40</td><td>0.14</td><td>0.20</td></tr><tr><th><b>III.1*</b></th><td><i>Brycon amazonicus</i></td><td>4.7</td><td>4.0</td><td>11.0</td><td>13.5</td><td>14.7</td><td>0.75</td><td>1.09</td><td>0.92</td><td>0.75</td><td>0.85</td><td>0.35</td><td>0.32</td><td>0.05</td><td>0.05</td></tr></tbody></table>
Table 3 in New record of endoparasitic Pseudempleurosoma haywardi (Monogenea: Dactylogyridae) in sillaginid fishes from Thailand, with updates on host range, zoogeography, and morphological variation
<p>Table 3. Measurement characteristics of the <i>Pseudempleurosoma haywardi</i> from the original description and current study. All measurements are given in micrometres (µm).</p><table><tbody><tr><th></th><th><b>Theisen et al. (2017)</b></th><th><b>Theisen et al. (2017)</b></th><th><b>Present study</b></th></tr></tbody><tbody><tr><th>Fish host</th><td><i>Nibea soldado</i> (Sciaenidae)</td><td><i>Otolithes ruber</i> (Sciaenidae)</td><td><i>Sillago aeolus</i> (Sillaginidae)</td></tr><tr><th>Site of infection</th><td>oesophagus/proximal stomach</td><td>oesophagus/proximal stomach</td><td>stomach</td></tr><tr><th>Study area</th><td>Pacific: off South Central Java, Indonesia</td><td>Pacific: off South Central Java, Indonesia</td><td>upper Gulf of Thailand</td></tr><tr><th>Bodya</th><td>588–1295 (971) × 181–361 (289)</td><td>582–937 (757) × 161–305 (230)</td><td>1000–2112 (1468) × 221–362 (294)</td></tr><tr><th>Opisthaptora</th><td>53–84 (66) × 101–142 (116)</td><td>58–88 (71) × 87–137 (119)</td><td>80–103 (91) × 139–167 (147)</td></tr><tr><th>Pharynxa</th><td>40–67 (52) × 40–63 (48)</td><td>44–64 (53) × 42–55 (47)</td><td>58–79 (73) × 54–88 (75)</td></tr><tr><th>Ovarya</th><td>44–101 (77) × 32–74 (55)</td><td>40–64 (52) × 28–62 (39)</td><td>60–99 (86) × 56–71 (61)</td></tr><tr><th>Testisa</th><td>39–95 (76) × 26–57 (41)</td><td>45–68 (56) × 29–47 (34)</td><td>58–100 (73) × 34–57 (40)</td></tr><tr><th>Dorsal anchorb</th><td>59–61 (60)</td><td>58–64 (61)</td><td>57–68 (61)</td></tr><tr><th>Dorsal bara</th><td>12–21(19) × 12–17 (15)</td><td>19–20 (20) × 12–17 (15)</td><td>17–22 (19) × 10–21 (14)</td></tr><tr><th>Ventral anchorb</th><td>14–16 (15)</td><td>14–18 (16)</td><td>15–17 (16)</td></tr><tr><th>Attached ventral barb</th><td>8–18 (11)</td><td>10–16 (13)</td><td>14–18 (16)</td></tr><tr><th>Detached ventral barb</th><td>17–21 (19)</td><td>13–20 (17)</td><td>20–22 (21)</td></tr><tr><th>Marginal hooksb</th><td>13–16 (15)</td><td>13–16 (15)</td><td>11–18 (14)</td></tr><tr><th>Male copulatory organ (MCO)b</th><td>29–51 (42)</td><td>33–52 (45)</td><td>53–57 (55)</td></tr><tr><th>Accessory piece of MCOb</th><td>14–23 (20)</td><td>5–19 (17)</td><td>20–23 (22)</td></tr><tr><th>Muscular genital atriuma</th><td>21–39 (29) × 20–31 (25)</td><td>20–26 (22) × 17–24 (20)</td><td>34–41 (37) × 30–32 (31)</td></tr><tr><th>Egga</th><td>56–72 (67) × 39–59 (50)</td><td>49–78 (68) × 33–59 (50)</td><td>57–97 (71) × 51–84 (64)</td></tr><tr><th>Egg’s filament</th><td>Absent</td><td>Absent</td><td>Absent</td></tr></tbody></table><p><sup>ashown</sup> as length × width</p><p><sup>bshown</sup> as length</p>
Table 2 in New record of endoparasitic Pseudempleurosoma haywardi (Monogenea: Dactylogyridae) in sillaginid fishes from Thailand, with updates on host range, zoogeography, and morphological variation
<p>Table 2. Sequence data of 28S rRNA region of current monogeneans and their related monogeneans acquired from the NCBI database. Taxa with asterisks (*) denote their categorisation in the family Ancyrocephalidae according to the NCBI database.</p><table><tbody><tr><th><b>Species</b></th><th><b>Accession number</b></th><th><b>Reference</b></th></tr><tr><th><b>Family Dactylogyridae</b></th></tr></tbody><tbody><tr><th><i>Actinocleidus recurvatus</i> *</th><td>AJ969951</td><td>Šimková et al. (2006)</td></tr><tr><th><i>Anacanthorus lepyrophallus</i></th><td>MH843718</td><td>Moreira et al. (unpublished)</td></tr><tr><th><i>Bravohollisia tecta</i> *</th><td>KJ571012</td><td>Sun et al. (unpublished)</td></tr><tr><th><i>Cichlidogyrus arthracanthus</i> *</th><td>HQ010022</td><td>Mendlová et al. (2010)</td></tr><tr><th><i>Dactylogyrus bicornis</i></th><td>KY629345</td><td>Šimková et al. (2017)</td></tr><tr><th><i>Dactylogyrus extensus</i></th><td>AJ969944</td><td>Mendlová et al. (2010)</td></tr><tr><th><i>Demidospermus mortenthaleri</i></th><td>KP056245</td><td>Mendoza-Palmero et al. (2015)</td></tr><tr><th><i>Diaphorocleidus magnus</i> *</th><td>MZ408903</td><td>Zago et al. (2021)</td></tr><tr><th><i>Diaphorocleidus neotropicalis</i> *</th><td>MZ408906</td><td>Zago et al. (2021)</td></tr><tr><th><i>Enterogyrus coronatus</i> *</th><td>HQ010030</td><td>Mendlová et al. (2010)</td></tr><tr><th><i>Enterogyrus malmbergi</i> *</th><td>MN152976</td><td>Zhang (unpublished)</td></tr><tr><th><i>Euryhaliotrema pirulum</i> *</th><td>AY820618</td><td>Plaisance et al. (2005)</td></tr><tr><th><i>Haliotrematoides guttata</i> *</th><td>HQ615993</td><td>Soler-Jimenez et al. (unpublished)</td></tr><tr><th><i>Haliotrematoides spinatus</i> *</th><td>HQ615995</td><td>Soler-Jimenez et al. (unpublished)</td></tr><tr><th><i>Heteropriapulus simplex</i></th><td>MF116372</td><td>Acosta et al. (2017)</td></tr><tr><th><i>Ligophorus imitans</i> *</th><td>JN996813</td><td>Blasco-Costa et al. (2012)</td></tr><tr><th><i>Ligophorus vanbenedenii</i> *</th><td>JN996801</td><td>Blasco-Costa et al. (2012)</td></tr><tr><th><i>Metahaliotrema subancistroides</i> *</th><td>EU836210</td><td>Sun & Yang (unpublished)</td></tr><tr><th><i>Mexicana rubra</i></th><td>KY553147</td><td>Camargo (2017)</td></tr><tr><th><i>Nanayella fluctuatrium</i></th><td>MG001327</td><td>Acosta et al. (2018)</td></tr><tr><th><i>Onchocleidus similis</i> *</th><td>AJ969938</td><td>Šimková et al. (2006)</td></tr><tr><th><i>Paradiplectanotrema klimpeli</i></th><td>MG763101</td><td>Theisen et al. (2018)</td></tr><tr><th><i>Protogyrodactylus hainanensis</i></th><td>DQ157653</td><td>Wu et al. (2006)</td></tr><tr><th><i>Pseudempleurosoma haywardi</i></th><td>MF115715</td><td>Theisen et al. (2017)</td></tr><tr><th><i>Pseudempleurosoma haywardi</i> (MN28-1)</th><td>ON969400</td><td>Present study</td></tr><tr><th><i>Pseudempleurosoma haywardi</i> (MN28-3)</th><td>ON969401</td><td>Present study</td></tr><tr><th><i>Sciadicleithrum bravohollisae</i></th><td>KY305879</td><td>Wu et al. (2006)</td></tr><tr><th><i>Sciadicleithrum meekii</i></th><td>KY305889</td><td>Mendoza-Palmero et al. (2017)</td></tr><tr><th><i>Scutogyrus longicornis</i> *</th><td>HQ010035</td><td>Mendlová et al. (2010)</td></tr><tr><th><i>Tetrancistrum indicum</i> *</th><td>MN179335</td><td>Al-Jufaili (unpublished)</td></tr><tr><th><i>Urocleidoides digitabulum</i></th><td>MT556796</td><td>Zago et al. (2020)</td></tr><tr><th><i>Vancleaveus janauacaensis</i></th><td>KP056247</td><td>Mendoza-Palmero et al. (2015)</td></tr><tr><th><b>Family Diplectanidae</b> (outgroup)</th></tr><tr><th><i>Dolicirroplectanum lacustre</i></th><td>MK937579</td><td>Kmentová et al. (2020)</td></tr><tr><th><i>Paradiplectanum sillagonum</i></th><td>AY553626</td><td>Wu et al. (2005)</td></tr><tr><th><i>Pseudorhabdosynochus grouperi</i></th><td>AY553628</td><td>Wu et al. (2005)</td></tr></tbody></table>
genomic sequencies of phages (prokaryotic vriuses) and their hosts
<p>This repository contains data relevant to the reserach <a href="https://github.com/yoheyokubo/MCL4PHI">Multi-Instance Contrastive Learning with Binomial K-Mers for Phage Host Interaction Prediction</a>. It is comprised of the preprocessed data (<em>data_preprocessed.zip</em>) to quickly reproduce our results and the raw genomic sequencies (<em>data_raw.zip</em>) of phages and hosts, originally from <a href="https://github.com/KennthShang/CHERRY">CHERRY's dataset</a>.</p>
FIGURE 4. Immature stages. A, first instar. B, second instar. C, third instar. D, fourth instar. E in A new species of Coelidiana Oman (Hemiptera: Cicadellidae: Neocoelidiinae) from Brazil with key to Brazilian species, description of immature stages, and notes about parasitoids and host plant
FIGURE 4. Immature stages. A, first instar. B, second instar. C, third instar. D, fourth instar. E, fifth instar. Scale bar in mm
FIGURE 2 in A new species of Coelidiana Oman (Hemiptera: Cicadellidae: Neocoelidiinae) from Brazil with key to Brazilian species, description of immature stages, and notes about parasitoids and host plant
FIGURE 2. Coelidiana aroeira sp. nov., paratype female. A, posterior portion of abdomen, ventral view. B, posterior portion of abdomen, lateral view. C, sternite VII and inner sternite VIII, ventral view. D, pygofer and anal tube, lateral view. E, first valvifer and first valvula of ovipositor, lateral view. F, apex of first valvula, lateral view. G, second valvifer and second valvula of ovipositor, lateral view. H, apex of second valvula, lateral view. I, gonoplac, lateral view. J, apex of gonoplac, lateral view. Scale bars in mm.
FIGURE 1 in A new species of Coelidiana Oman (Hemiptera: Cicadellidae: Neocoelidiinae) from Brazil with key to Brazilian species, description of immature stages, and notes about parasitoids and host plant
FIGURE 1. Coelidiana aroeira sp. nov., holotype male. A, head and thorax, dorsal view. B, head, frontal view. C, head and thorax, lateral view. D, forewing. E, genital capsule. F, pygofer and anal tube, lateral view. G, valve and subgenital plates, ventral view. H, valve and subgenital plate, lateral view. I, styles and connective, dorsal view. J, style, lateral view. K, aedeagus, lateral view. L, aedeagus, posterior view. Scale bars in mm.
FIGURE 6 in A new species of Coelidiana Oman (Hemiptera: Cicadellidae: Neocoelidiinae) from Brazil with key to Brazilian species, description of immature stages, and notes about parasitoids and host plant
FIGURE 6. Tree of Schinus terebinthifolia (Aroeira-Pimenteira) studied at Curitiba (Paraná) and detail of growing fruits.
FIGURE 5 in A new species of Coelidiana Oman (Hemiptera: Cicadellidae: Neocoelidiinae) from Brazil with key to Brazilian species, description of immature stages, and notes about parasitoids and host plant
FIGURE 5. Fifth instar nymph terminalia of Coelidiana aroeira sp. nov. A, Male plates. B, Female plates.
FIGURES 78–83 in Exploring the diversity of Gracillariidae (Lepidoptera) in South Africa: host plants, distribution, and DNA barcoding analysis, with the description of nine new species
FIGURES 78–83. Immature stages of South African Gracillariidae. 78, Phodoryctis tephrosiella, mines on Tephrosia rhodesica (Fabaceae). Gauteng, Tshwane, A. Sharp leg. 79, Conopobathra carbunculata, mines on Peltophorum africanum (Fabaceae), Limpopo, York, A. & I. Sharp leg. 80, Phyllonorycter grewiella, mine on Grewia hexamita (Malvaceae), A. & I. Sharp leg. 81, P. pseudogrewiella sp. nov., mines on Grewia flavescens (Malvaceae), Limpopo, Hoedspruit, A. & I. Sharp leg. 82, P. pseudogrewiella sp. nov., larva, ibidem. 83, P. pseudogrewiella sp. nov., mines and pupae, ibidem.
FIGURES 67–72 in Exploring the diversity of Gracillariidae (Lepidoptera) in South Africa: host plants, distribution, and DNA barcoding analysis, with the description of nine new species
FIGURES 67–72. Immature stages of South African Gracillariidae. 67, Conopomorphina aptata, mine on Schotia brachypetala (Fabaceae), Limpopo, Hoedspruit, A. & I. Sharp leg. 68, Acrocercops syzygiena, mine on Syzygium cordatum (Myrtaceae), Gauteng, Tshwane, A. & I. Sharp leg. 69, A. syzygiena, larva, ibidem. 70, A. combreticola, mine on Combretum zeyheri (Combretaceae) Gauteng, Tshwane, A. Sharp leg. 71, Cryptolectica capnodecta, larva on Syzygium cordatum (Myrtaceae), Limpopo, Hoedspruit, A. & I. Sharp leg. 72, C. terminalina, mine on Terminalia sericea (Combretaceae), A. & I. Sharp leg.
FIGURES 84−88 in Exploring the diversity of Gracillariidae (Lepidoptera) in South Africa: host plants, distribution, and DNA barcoding analysis, with the description of nine new species
FIGURES 84−88. Immature stages of South African Gracillariidae species. 84, Cameraria melhaniella sp. nov., larva on Melhania acuminata (Malvaceae), Limpopo, Hoedspruit, A. & I. Sharp leg. 85, Metriochroa pergulariae, mine on Pergularia daemia (Apocynaceae), Limpopo, Hoedspruit, A. & I. Sharp leg. 86, Phyllocnistis allisonae, mine on Protea rubropilosa (Proteaceae), Limpopo, Lopez Vaamonde leg. 87, Phyllocnistis magalismontani sp. nov., mine on Englerophytum magalismontanum (Sapotaceae), Limpopo, Hoedspruit, leg. A. & I. Sharp. 88, Phyllocnistis faureae, mine on Faurea saligna (Proteaceae), Gauteng, Tshwane, leg. A. Sharp.
FIGURES 61−66 in Exploring the diversity of Gracillariidae (Lepidoptera) in South Africa: host plants, distribution, and DNA barcoding analysis, with the description of nine new species
FIGURES 61−66. Immature stages of South African Gracillariidae. 61, Caloptilia sp., larva on Cryptocarya transvaalensis (Lauraceae), Limpopo, Lekgalameetse N. R., A. & I. Sharp leg. 62, C. cataractias, larva on Rhynchosia minima (Fabaceae), Limpopo, Hoedspruit, A. & I. Sharp leg. 63, Macarostola noellineae, larva on Syzygium cordatum (Myrtaceae), Limpopo, Hoedspruit, A. & I. Sharp leg. 64, Ectropina spirostachydis sp. nov., larva on Spirostachys africana (Euphorbiaceae), Limpopo, Hoedspruit, A. & I. Sharp leg. 65, Cuphodes melanostola, mine on Euclea divinorum (Ebenaceae), Limpopo, Hoedspruit, A. & I. Sharp leg. 66, Conopomorphina ochnivora, Gauteng, Magaliesburg, on Ochna pretoriensis, (Ochnaceae), H. Staude leg.
FIGURES 58–60 in Exploring the diversity of Gracillariidae (Lepidoptera) in South Africa: host plants, distribution, and DNA barcoding analysis, with the description of nine new species
FIGURES 58–60. Female genitalia of South African Gracillariidae. 58-59, Phyllocnistis magalismontani sp. nov., paratype: 58, lateral view; 59, signa. 60, P. allisonae sp. nov., holotype: ventral view. (All scale bar 190 μm).
FIGURES 56–57 in Exploring the diversity of Gracillariidae (Lepidoptera) in South Africa: host plants, distribution, and DNA barcoding analysis, with the description of nine new species
FIGURES 56–57. Female genitalia of South African Gracillariidae. 56, Telamoptilia cordati sp. nov., paratype: ventral view. 57, Phyllonorycter pseudogrewiella sp. nov., holotype: lateral view. (All scale bar 190 μm).
FIGURES 44–46 in Exploring the diversity of Gracillariidae (Lepidoptera) in South Africa: host plants, distribution, and DNA barcoding analysis, with the description of nine new species
FIGURES 44–46. Male genitalia of South African Gracillariidae. Phodoryctis tephrosiella sp. nov.: 44, holotype, ventral view; 45, phallus with bulbus ejaculatorius; 46, segment VIII in ventral view (ae: aedeagus; pb: phallobase; be: bulbus ejaculatorius). (All scale bars 190 μm).
FIGURES 25−30 in Exploring the diversity of Gracillariidae (Lepidoptera) in South Africa: host plants, distribution, and DNA barcoding analysis, with the description of nine new species
FIGURES 25−30. Forewing pattern of South African Gracillariidae. 25, Leucocercops curatellifoliae sp. nov., Limpopo. 26, Phodoryctis tephrosiella sp. nov., Gauteng. 27, Telamoptilia cordati sp. nov., South Africa, Limpopo. 28, Telamoptilia sp., Madagascar. 29, Cameraria melhaniella sp. nov., Limpopo. 30, Phyllonorycter pseudogrewiella sp. nov., Limpopo.
FIGURES 13–18 in Exploring the diversity of Gracillariidae (Lepidoptera) in South Africa: host plants, distribution, and DNA barcoding analysis, with the description of nine new species
FIGURES 13–18. Adults of South African Gracillariidae. 13, Cryptolectica capnodecta, Limpopo, Hoedspruit, A. & I. Sharp leg. 14, C. terminalina, Limpopo, Hoedspruit, A. & I. Sharp leg. 15, Dialectica pyramidota, Limpopo, Hoedspruit, A. & I. Sharp leg. 16, Amblyptila cynanchi, Western Cape, Knysna, S. Mecenero leg. 17, Leucocercops dasmophora, Gauteng, Tshwane, A. & I. Sharp leg. 18, L. curatellifoliae sp. nov. Limpopo, Hoedspruit, A. & I. Sharp leg.
ScienceDex guides
Understand access before you commit
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.