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opennotspecifiedNov 2019View details →

FIGURES 117–118. FIGURE 117 in Rearrangements in some species groups of Amblycerus Thunberg, 1815 (Coleoptera: Chrysomelidae: Bruchinae) including keys, description of a new species, new host plant and distributional records

FIGURES 117–118. FIGURE 117. Map with the geographical distribution of A. crassipunctatus and A. dispar. Leaked symbols refer to bibliography data. FIGURE 118. Map with the geographical distribution of A. insuturatus and A. schwarzi. Leaked symbols refer to bibliography data.

opennotspecifiedNov 2019View details →

FIGURES 35–40 in Rearrangements in some species groups of Amblycerus Thunberg, 1815 (Coleoptera: Chrysomelidae: Bruchinae) including keys, description of a new species, new host plant and distributional records

FIGURES 35–40. Lateral. group dispar: 35. Amblycerus crassipunctatus, 36. A. dispar, 37. A. insuturatus, 38. A. schwarzi, 39. A. taeniopygus and 40. Amblycerus goianiensis Santos & Ribeiro-Costa, sp. n. Scale bars = 1.0 mm.

opennotspecifiedJun 2023View details →

Figs 15–20 in Redescription of the parasitic wasp Melittobia sosui Dahms, 1984 (Hymenoptera: Eulophidae), with records on its new hosts in Vietnam

Figs 15–20. Melittobia sosui Dahms, male: 15 — head, frontal view; 16 — mandible; 17 — antenna, ventral view; 18 — mesosoma and metasoma, dorsal view; 19 — mid leg; 20 — habitus, lateral view. Рис. 15–20. Melittobia sosui Dahms, самец: 15 — голова, вид спереди; 16 — нижнЯЯ челюсть; 17 — антенна, вид сниЗу; 18 — меЗосома и метасома, вид сверху; 19 — среднЯЯ ножка; 20 — габитус, вид сбоку.

opennotspecifiedDec 2021View details →

Figs. 1–2 in Bionomics and New Host Plant Records of the Australian Trunk-Boring Cycad Weevils (Coleoptera: Curculionidae)

Figs. 1–2. Microhabitat of Demyrsus meleoides in northern New South Wales. 1) Infested trunk of Lepidozamia peroffskyana in which adults of D. meleoides were found; 2) Adults of D. meleoides lodged between decomposed and intact parts of the trunk.

opennotspecifiedDec 2021View details →

Figs. 3–4 in Bionomics and New Host Plant Records of the Australian Trunk-Boring Cycad Weevils (Coleoptera: Curculionidae)

Figs. 3–4. Cycad host of Siraton internatus in northern inland New South Wales. 3) Natural population of Macrozamia polymorpha near Baradine (30°55′04.1′′S, 149°16′21.0′′E); 4) Fresh female cone with mucilaginous sap, in which S. internatus adults were found crawling around the base of the cone.

Fig. 7 in The lanternflies of the Penthicodes (Ereosoma) atomaria+ species group in Thailand: New records and host plants (Hemiptera: Fulgoridae)

Fig. 7. Penthicodes (Ereosoma) pulchella Guérin-Méneville, 1838 in nature (photograph by K. Jiaranaisakul). A, on Shorea obtusa (Dipterocarpaceae). B, hiding behaviour under the bark of Shorea obtusa. C, on Lagerstroemia cf. floribunda (Lythraceae). D, hiding behaviour under the bark of Lagerstroemia cf. floribunda.

Fig. 3 in The lanternflies of the Penthicodes (Ereosoma) atomaria+ species group in Thailand: New records and host plants (Hemiptera: Fulgoridae)

Fig. 3. Penthicodes (Ereosoma) spp. Male genitalia. A–D. P. (Ereosoma) atomaria. A, pygofer, anal tube and gonostyli, left lateral view. B, anal tube, posterior view. C, anal tube and pygofer, dorsal view. D, pygofer and gonostyli, posteroventral view. E–H. P. (Ereosoma) pulchella. E, pygofer, anal tube and gonostyli, left lateral view. F, anal tube, posterior view. G, anal tube and pygofer, dorsal view. H, pygofer and gonostyli, posteroventral view. I–L. P. (Ereosoma) warleti. I, pygofer, anal tube and gonostyli, left lateral view. J, anal tube, posterior view. K, anal tube and pygofer, dorsal view. L, pygofer and gonostyli, posteroventral view. An: anal tube; G: gonostyli; Py: pygofer. Scale 2 mm.

Fig. 2 in The lanternflies of the Penthicodes (Ereosoma) atomaria+ species group in Thailand: New records and host plants (Hemiptera: Fulgoridae)

Fig. 2. Penthicodes (Ereosoma) warleti Constant, 2010 in nature. A, Ratchaburi, Suan Phueng, 11.X.2011 (photograph by K. Jiaranaisakul). B, habitat in Suan Phueng, 27.X.2017 (photograph by K. Jiaranaisakul). C–D, Nakhon Ratchasima, Khao Yai National Park, 23.III.2015 (photograph by R. Hongsaeng). E, Petchabun, Nam Nao National Park, 15.IV.2012 (photograph by N. Makbun). F, Surat Thani, Khao Sok National Park, IV.2008 (photograph by A. Mommerency).

Fig. 5 in The lanternflies of the Penthicodes (Ereosoma) atomaria+ species group in Thailand: New records and host plants (Hemiptera: Fulgoridae)

Fig. 5. Penthicodes (Ereosoma) atomaria (Weber, 1801) in nature (photographs by K. Jiaranaisakul). A, on Castanopsis diversifolia (Fagaceae). B, on Lagerstroemia macrocarpa (Lythraceae).

Fig. 1 in The lanternflies of the Penthicodes (Ereosoma) atomaria+ species group in Thailand: New records and host plants (Hemiptera: Fulgoridae)

Fig. 1. Penthicodes (Ereosoma) warleti Constant, 2010. A–D, ♂. A, habitus, dorsal view. B, head and prothorax, lateral view. C, habitus, ventral view. D, head, pro- and mesonotum, dorsal view. E, ♀, habitus, dorsal view.

opennotspecifiedMar 2015View details →

Figure 1 in Interaction between Tephritidae (Insecta, Diptera) and plants of the family Asteraceae: new host and distribution records for the state of Rio Grande do Sul, Brazil

Figure 1. Localities in Rio Grande do Sul, Brazil, where the fauna of Tephritidae (Dip* tera) from capitula of Asteraceae was sampled.

FIGURE 3. A. M in First record of Monalonion velezangeli (Hemiptera: Miridae) affecting avocado and cherimoya (Annona cherimola) as new hosts in Ecuador

FIGURE 3. A. M. velezangeli adult in vivo. B. Antennae with four segments. C. Rostrum of M. velezangeli with its four segments. D and E. Coloration diversity in the M. velezangeli pronotum (P), scutellum (S). F and G. Coloration diversity in the legs of M. velezangeli and creamy white strip in the middle of the femurs (CWS). H and I. Coloration diversity in forewings in cuneus (Cu) and corium (Co), spots inside (Si) and outside the vein in the membrane (Me).

FIGURE 1. A in First record of Monalonion velezangeli (Hemiptera: Miridae) affecting avocado and cherimoya (Annona cherimola) as new hosts in Ecuador

FIGURE 1. A. Nymph of M. velezangeli on an avocado plant. B. Adult of M. velezangeli on an avocado fruit. C. M. velezangeli bites on young avocado branches. D. Damage to small fruit of 2.2 and 2.4 cm in polar diameter.

FIGURE 4 in First record of Monalonion velezangeli (Hemiptera: Miridae) affecting avocado and cherimoya (Annona cherimola) as new hosts in Ecuador

FIGURE 4. Structures of the male genitalia of M. velezangeli. A. Aedeagus: teak opening (at), teak (te), endosoma (en), seminal duct (sd), phallus base (bp), captured process. B. Left paramere: basal region (br), paramere body (pb), apical region (ar). C. Right paramere: basal region (br), paramere body (pb), apical region (ar). D. Agarose gel with PCR products for the COI fragment of five of the collected samples (MM= molecular weight marker, CN = negative control).

FIGURE 2. Confirmation test for M in First record of Monalonion velezangeli (Hemiptera: Miridae) affecting avocado and cherimoya (Annona cherimola) as new hosts in Ecuador

FIGURE 2. Confirmation test for M. velezangeli damage in avocado and cherimoya. A. Healthy fruit. B. Fruit confined with an adult M. velezangeli. C. Fruit of 6.3 cm in polar diameter with damage due to the bug's puncture. D. Fruit confined with an adult M. velezangeli. E. Fruit affected by M. velezangeli. F. Fruit with recent pitting (left) and fruit with old pitting (right) and beginnings of a saprophytic fungal infection.

opencc-by-4.0Apr 2023View details →

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

Table 3. Measurement characteristics of the Pseudempleurosoma haywardi from the original description and current study. All measurements are given in micrometres (µm).<table><tbody><tr><th></th><th>Theisen et al. (2017)</th><th>Theisen et al. (2017)</th><th>Present study</th></tr></tbody><tbody><tr><th>Fish host</th><td>Nibea soldado (Sciaenidae)</td><td>Otolithes ruber (Sciaenidae)</td><td>Sillago aeolus (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>ashown as length × widthbshown as length

opencc-by-4.0Apr 2023View details →

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

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.<table><tbody><tr><th>Species</th><th>Accession number</th><th>Reference</th></tr><tr><th>Family Dactylogyridae</th></tr></tbody><tbody><tr><th>Actinocleidus recurvatus *</th><td>AJ969951</td><td>&Scaron;imková et al. (2006)</td></tr><tr><th>Anacanthorus lepyrophallus</th><td>MH843718</td><td>Moreira et al. (unpublished)</td></tr><tr><th>Bravohollisia tecta *</th><td>KJ571012</td><td>Sun et al. (unpublished)</td></tr><tr><th>Cichlidogyrus arthracanthus *</th><td>HQ010022</td><td>Mendlová et al. (2010)</td></tr><tr><th>Dactylogyrus bicornis</th><td>KY629345</td><td>&Scaron;imková et al. (2017)</td></tr><tr><th>Dactylogyrus extensus</th><td>AJ969944</td><td>Mendlová et al. (2010)</td></tr><tr><th>Demidospermus mortenthaleri</th><td>KP056245</td><td>Mendoza-Palmero et al. (2015)</td></tr><tr><th>Diaphorocleidus magnus *</th><td>MZ408903</td><td>Zago et al. (2021)</td></tr><tr><th>Diaphorocleidus neotropicalis *</th><td>MZ408906</td><td>Zago et al. (2021)</td></tr><tr><th>Enterogyrus coronatus *</th><td>HQ010030</td><td>Mendlová et al. (2010)</td></tr><tr><th>Enterogyrus malmbergi *</th><td>MN152976</td><td>Zhang (unpublished)</td></tr><tr><th>Euryhaliotrema pirulum *</th><td>AY820618</td><td>Plaisance et al. (2005)</td></tr><tr><th>Haliotrematoides guttata *</th><td>HQ615993</td><td>Soler-Jimenez et al. (unpublished)</td></tr><tr><th>Haliotrematoides spinatus *</th><td>HQ615995</td><td>Soler-Jimenez et al. (unpublished)</td></tr><tr><th>Heteropriapulus simplex</th><td>MF116372</td><td>Acosta et al. (2017)</td></tr><tr><th>Ligophorus imitans *</th><td>JN996813</td><td>Blasco-Costa et al. (2012)</td></tr><tr><th>Ligophorus vanbenedenii *</th><td>JN996801</td><td>Blasco-Costa et al. (2012)</td></tr><tr><th>Metahaliotrema subancistroides *</th><td>EU836210</td><td>Sun & Yang (unpublished)</td></tr><tr><th>Mexicana rubra</th><td>KY553147</td><td>Camargo (2017)</td></tr><tr><th>Nanayella fluctuatrium</th><td>MG001327</td><td>Acosta et al. (2018)</td></tr><tr><th>Onchocleidus similis *</th><td>AJ969938</td><td>&Scaron;imková et al. (2006)</td></tr><tr><th>Paradiplectanotrema klimpeli</th><td>MG763101</td><td>Theisen et al. (2018)</td></tr><tr><th>Protogyrodactylus hainanensis</th><td>DQ157653</td><td>Wu et al. (2006)</td></tr><tr><th>Pseudempleurosoma haywardi</th><td>MF115715</td><td>Theisen et al. (2017)</td></tr><tr><th>Pseudempleurosoma haywardi (MN28-1)</th><td>ON969400</td><td>Present study</td></tr><tr><th>Pseudempleurosoma haywardi (MN28-3)</th><td>ON969401</td><td>Present study</td></tr><tr><th>Sciadicleithrum bravohollisae</th><td>KY305879</td><td>Wu et al. (2006)</td></tr><tr><th>Sciadicleithrum meekii</th><td>KY305889</td><td>Mendoza-Palmero et al. (2017)</td></tr><tr><th>Scutogyrus longicornis *</th><td>HQ010035</td><td>Mendlová et al. (2010)</td></tr><tr><th>Tetrancistrum indicum *</th><td>MN179335</td><td>Al-Jufaili (unpublished)</td></tr><tr><th>Urocleidoides digitabulum</th><td>MT556796</td><td>Zago et al. (2020)</td></tr><tr><th>Vancleaveus janauacaensis</th><td>KP056247</td><td>Mendoza-Palmero et al. (2015)</td></tr><tr><th>Family Diplectanidae (outgroup)</th></tr><tr><th>Dolicirroplectanum lacustre</th><td>MK937579</td><td>Kmentová et al. (2020)</td></tr><tr><th>Paradiplectanum sillagonum</th><td>AY553626</td><td>Wu et al. (2005)</td></tr><tr><th>Pseudorhabdosynochus grouperi</th><td>AY553628</td><td>Wu et al. (2005)</td></tr></tbody></table>

opennotspecifiedFeb 2021View details →

Figure 7 in New hosts and distribution records for bopyrid isopods parasitising alpheid shrimps (Decapoda, Alpheidae) in the SW Gulf of Mexico and Mexican Caribbean

Figure 7. Parabopyrella mortenseni (Nierstraz and Brender à Brandis, 1929). a) first oostegite of juvenile female (CNCR 34975) parasitising Alpheus normanni, internal view; b) juvenile female (CNCR 35023) parasitising A. cristulifrons, dorsal view; c) antenna and antennule of female CNCR 35023; d) maxilliped of female CNCR 35023. Scale bar = 0.5 mm in a; 1.0 mm in b; 0.2 mm in c-d.

opennotspecifiedFeb 2021View details →

Figure 5 in New hosts and distribution records for bopyrid isopods parasitising alpheid shrimps (Decapoda, Alpheidae) in the SW Gulf of Mexico and Mexican Caribbean

Figure 5. Capitetragonia alphei (Richardson, 1900), CNCR 34973. a) antenna and antennule of female; b) maxilliped; c) female pleon, ventral view; d) fifth pereopod of male. Scale bar = 0.5 mm in a; 1.0 mm in b-c; 0.1 mm in d.