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opennotspecifiedFeb 2024View details →

FIGURES 38–43. 38 in Studies in the New World tribe Anisoscelini Laporte, 1832 (Heteroptera: Coreidae: Coreinae): updated distributions, nomenclatural changes, and keys to the genera of the tribe and the species of Anisoscelis Latreille, 1829 and Bitta Osuna, 1984

FIGURES 38–43. 38. Kalinckascelis bambusae Brailovsky; 39. Mamurius mopsus Stål; 40. Sephinioides ugaldei Brailovsky; 41. Malvanaioides intrincata Brailovsky; 42. Leptopelios ventus Brailovsky; 43. Coribergia declivicollis (Berg).

Fig. 6 in Three new tribes in Myrtaceae and reassessment of Kanieae

Fig. 6. Vascularisation in skeletonised fruits. (a) Kania sp., scale bar: 1 mm; and (b, c) Tristaniopsis collina, scale bars: 2 mm.

Fig. 5 in Three new tribes in Myrtaceae and reassessment of Kanieae

Fig. 5. Cuticles of several species from the tribe Kanieae. (a–f) SEM images. (a) Kania eugenioides; scale bar: 50 μm. (b) Barongia lophandra; scale bar: 50 μm. (c) Kania urdanetensis (Elmer) Peter G.Wilson; scale bar: 50 μm. (d) Metrosideros robusta; scale bar: 50 μm. (e) Tristaniopsis laurina; scale bar: 20 μm. Note cuticular striations radiating from the water stomata and the papillose texture in a–e (but not as well developed in Metrosideros and Tristaniopsis). (f) Xanthomyrtus montivaga; scale bar: 20 μm. The cuticles of Xanthomyrtus lack water stomata entirely, as well as any associated cuticle striations.

Fig. 4 in Three new tribes in Myrtaceae and reassessment of Kanieae

Fig. 4. Examples of the most common forms of stomatal distribution in cuticles from across the Myrtaceae. Light microscopy. (a) Cuticle of Metrosideros (Carpolepis) laurifolia, showing an even distribution of stomata, and (b) Lophostemon confer-tus, showing separation of stomata by major and minor leaf venation into vein islets or areolae. Scale bars: 500 μm.

Fig. 3 in Three new tribes in Myrtaceae and reassessment of Kanieae

Fig. 3. Examples of variation in stomatal distribution. Light microscopy. (a) Cuticle of Kania eugenioides, showing 'clumping' of stomata with no clear distribution into vein islets or areolae; scale bar: 200 μm. and (b) A close up of the clumped stomata, showing a disorganised distribution in K. eugenioides. (c) Xanthomyrtus montivaga, showing an alternative form of aggregation of stomata into distinct zones, with large non-stomatal areas between zones, with no clear relation to underlying venation; scale bar: 200 μm. (d) A close up of the aggregated stomata. There are no spaces between any of the subsidiary cells of stomata in Xanthomyrtus species, and stomata are approximately half the size (~5 μm).

Fig. 2. Bayesian 50 in Three new tribes in Myrtaceae and reassessment of Kanieae

Fig. 2. Bayesian 50% majority rule consensus tree of combined nuclear data. Values shown on tree indicate clade support from Bayesian posterior probabilities (PP, above branches) and jackknife values from maximum parsimony analysis of>50% (jk, below). Thick lines received strong support 1.00 PP and jk ≥ 90%. New or revised tribal assignments are indicated in bold.

Fig. 1. Bayesian 50 in Three new tribes in Myrtaceae and reassessment of Kanieae

Fig. 1. Bayesian 50% majority-rule consensus tree of combined plastid data. Values shown on tree indicate clade support from Bayesian posterior probabilities (PP, above branches) and jackknife values from maximum parsimony analysis of>50% (jk, below). Thick lines received strong support 1.00 PP and jk ≥ 90%. New or revised tribal assignments are indicated in bold.

opennotspecifiedMar 2022View details →

Figs 20–27 in The longicorn beetle tribe Cerambycini Latreille, 1802 (Coleoptera: Cerambycidae: Cerambycinae) in the fauna of Asia. 17. A new species of the genus Spinidymasius Miroshnikov, 2017 from Borneo, with the description of the female of S. huedepohli (Vives, 2005) and new synonymy

Figs 20–27. Spinidymasius spp., genitalia: 20, 22, 24, 26 — S. pseudohuedepohli sp.n. (20, 22, 24 — holotype, male; 26 — paratype, female); 21, 23, 25, 27 — S. huedepohli (21, 23, 25 — holotype, male; 27 — female); 20–21 — apical part of tegmen, ventral view; 22– 23 — apical part of penis, ventral view; 24–25 — apical part of male tergite 8, dorsal view; 26–27 — coxites and styles, dorsal view. Рис. 20–27. Spinidymasius spp., гениталии: 20, 22, 24, 26 — S. pseudohuedepohli sp.n. (20, 22, 24 — голотип, самец; 26 — паратип, самка); 21, 23, 25, 27 — S. huedepohli (21, 23, 25 — голотип, самец; 27 — самка); 20–21 — верШиннаЯ часть тегмена, сниЗу; 22– 23 — верШиннаЯ часть пениса, сниЗу; 24–25 — верШиннаЯ часть 8-го тергита самца, сверху; 26–27 — кокситы и стилусы, сверху.

opennotspecifiedMar 2022View details →

Figs 1–7 in The longicorn beetle tribe Cerambycini Latreille, 1802 (Coleoptera: Cerambycidae: Cerambycinae) in the fauna of Asia. 17. A new species of the genus Spinidymasius Miroshnikov, 2017 from Borneo, with the description of the female of S. huedepohli (Vives, 2005) and new synonymy

Figs 1–7. Spinidymasius spp., habitus and labels: 1–2 — S. pseudohuedepohli sp.n.; 3–7 — S. huedepohli (4, 7 — photographs by Daniel Heffern); 1, 5–6 — holotypes; 2 — paratype; 1, 4–5 — males; 2–3, 7 — females. Рис. 1–7. Spinidymasius spp., обЩий вид и Этикетки: 1–2 — S. pseudohuedepohli sp.n.; 3–7 — S. huedepohli (4, 7 — фотографии Д. Хефферна); 1, 5–6 — голотипы; 2 — паратип; 1, 4–5 — самцы; 2–3, 7 — самки.

opennotspecifiedMar 2020View details →

Fig. 11 in Protopectinus pseudoparatinus - a new genus and species of soft winged flower beetle of the tribe Apalochrini (Coleoptera: Malachiidae) from East Africa

Fig. 11. Protopectinus pseudoparatinus Tshrernyshev gen. et sp.n., distribution map. Рис. 11. Protopectinus pseudoparatinus Tshrernyshev gen. et sp.n., карта распространениЯ.

opennotspecifiedMar 2020View details →

Figs 1–10 in Protopectinus pseudoparatinus - a new genus and species of soft winged flower beetle of the tribe Apalochrini (Coleoptera: Malachiidae) from East Africa

Figs 1–10. Protopectinus pseudoparatinus Tshrernyshev gen. et sp.n., holotype, male: 1 — external appearance, dorsal view; 2 — external appearance, lateral view; 3 — left antenna; 4 — left anterior tarsus; 5 — tibia and tarsus of left intermediate leg; 6 — femur of right intermediate leg; 7 — pygidium; 8 — ultimate abdominal ventrite; 9 — aedeagus, dorsal view; 10 — tegmen. Scale bars: 0.5 mm. Рис. 1–10. Protopectinus pseudoparatinus Tshrernyshev gen. et sp.n., голотип, самец: 1 — внеШний вид, дорЗально; 2 — внеШний вид латерально; 3 — левый усик; 4 — леваЯ переднЯЯ лапка; 5 — голень и лапка левой средней ноги; 6 — бедро правой средней ноги; 7 — пигидий (апикальный тергит); 8 — восьмой терминальный абдоминальный вентрит (апикальный стернит); 9 — Эдеагус, дорЗально; 10 — тегмен. МасШтаб: 0,5 мм.

opennotspecifiedMar 2022View details →

Figs 8–19 in The longicorn beetle tribe Cerambycini Latreille, 1802 (Coleoptera: Cerambycidae: Cerambycinae) in the fauna of Asia. 17. A new species of the genus Spinidymasius Miroshnikov, 2017 from Borneo, with the description of the female of S. huedepohli (Vives, 2005) and new synonymy

Figs 8–19. Spinidymasius spp.: 8, 10, 12, 14, 18 — S. pseudohuedepohli sp.n.; 9, 16–17 — S. ochraceovittatus; 11, 13, 15, 19 — S. huedepohli; 8–9, 12–13, 16, 18–19 — holotypes; 10, 14, 17 — paratypes; 8–9, 12–13, 16–19 — males; 10–11, 14–15 — females; 8, 10– 11 — habitus, ventral view; 9 — habitus, dorsal view; 12–17 — elytral apex; 18–19 — last (visible) abdominal sternite of male. Рис. 8–19. Spinidymasius spp.: 8, 10, 12, 14, 18 — S. pseudohuedepohli sp.n.; 9, 16–17 — S. ochraceovittatus; 11, 13, 15, 19 — S. huedepohli; 8–9, 12–13, 16, 18–19 — голотипы; 10, 14, 17 — паратипы; 8–9, 12–13, 16–19 — самцы; 10–11, 14–15 — самки; 8, 10– 11 — обЩий вид, сниЗу; 9 — обЩий вид, сверху; 12–17 — верШина надкрылий; 18–19 — последний (видимый) брЮШной стернит самца.

opennotspecifiedNov 2023View details →

TABLE 1 in On a new tribe, genus and species of Cypricercinae McKenzie, 1971 (Crustacea, Ostracoda, Cyprididae) from New Caledonia (Pacific Ocean)

TABLE 1. Non-marine ostracod species known from the New Caledonian archipelago (adapted from Kisseih et al. 2020—only published records shown). There are 14 accepted species and 4 uncertain species, indicated as “(?)”.<table><thead><tr><th>Species</th><th>Locality</th><th>Reference</th></tr><tr><th colspan="3">Family Darwinulidae Brady & Roberston, 1885</th></tr></thead><tbody><tr><th>1. Penthesilenula brasiliensis (Pinto & Kotzian, 1961)</th><td>Hienghène, Mt. Panié (Grande Terre)</td><td>Martens & Rossetti (2002)</td></tr><tr><th>2. Vestalenula marmonieri Rossetti & Martens, 1999</th><td>River Diahot, Ouegoa (Grande Terre)</td><td>Rossetti & Martens (1999)</td></tr><tr><th colspan="3">Family Cytherideidae Sars, 1925</th></tr><tr><th>3. Cyprideis australiensis Hartmann, 1978</th><td>Grande Terre</td><td>Hoibian et al. (2000, 2002)</td></tr><tr><th>4. Cyprideis consobrina (Brady, 1890)</th><td>Nouméa (Grande Terre)</td><td>Brady (1890), Maddocks (2007)</td></tr><tr><th colspan="3">Family Notodromadidae Kaufmann, 1900</th></tr><tr><th>5. Kennethia major (Méhes, 1939)</th><td>Canala (Grande Terre)</td><td>De Deckker (1979)</td></tr><tr><th>Syn.: Notodromas major Méhes, 1939</th><td></td><td>Méhes (1939)</td></tr><tr><th colspan="3">Family Cyprididae Baird, 1845</th></tr><tr><th colspan="3">Subfamily Cypricercinae McKenzie, 1971</th></tr><tr><th>6. Lithocypris peyia gen. et spec. nov.</th><td>Tribu du Peyia (Grande Terre)</td><td>Present paper</td></tr><tr><th>(?) Strandesia rouxi Méhes, 1939</th><td>Koné, Canala, La Foa (Grande Terre)</td><td>Méhes (1939)</td></tr><tr><th>7. Strandesia sanoamuangae Savatenalinton & Martens, 2010</th><td>several localities (Grande Terre)</td><td>Kisseih et al. (2020)</td></tr><tr><th>8. Strandesia mehesi Kisseih et al., 2020</th><td>several localities (Grande Terre)</td><td>Kisseih et al. (2020)</td></tr><tr><th colspan="3">Subfamily Herpetocypridinae Kaufmann, 1900</th></tr><tr><th>9. Caledromus robinsmithi Martens et al., 2023</th><td>Poindimié (Grande Terre)</td><td>Martens et al. (2023)</td></tr><tr><th>10. Candonocypris novaezelandiae (Baird, 1843)</th><td>La Foa (Grande Terre)</td><td>Martens et al. (2019)</td></tr><tr><th>Syn.: Candonopsis (sic) caledonica</th><td></td><td>Meisch et al. (2007)</td></tr><tr><th>Syn.: Herpetocypris caledonica Méhes, 1939</th><td></td><td>Méhes (1939)</td></tr><tr><th>Syn.: Candonocypris caledonica (Méhes, 1939)</th><td></td><td>De Deckker (1981)</td></tr><tr><th>Syn.: Herpetocypris caledonica var. minor Méhes, 1939</th><td></td><td>Méhes (1939)</td></tr><tr><th>11. Stenocypris major (Baird, 1859)</th><td>Canala, Koné (Grande Terre)</td><td>Martens et al. (2019)</td></tr><tr><th>Syn.: Stenocypris malcolmsoni Brady, 1886</th><td></td><td>Méhes (1939)</td></tr><tr><th>12. Stenocypris marginata Daday, 1910</th><td>Koné, Canala, La Foa (Grande Terre)</td><td>Méhes (1939)</td></tr><tr><th colspan="3">Subfamily Cyprinotinae Bronstein, 1947</th></tr><tr><th>(?) Cyprinotus cingalensis Brady, 1886</th><td>Loyalty Isl., Ovéa</td><td>Neale (1979)</td></tr><tr><th>13. Cyprinotus drubea Martens et al., 2019</th><td>Paita (Grande Terre)</td><td>Martens et al. (2019)</td></tr><tr><th colspan="3">Subfamily Cypridinae Baird, 1845</th></tr><tr><th>14. Cypris granulata (Daday, 1898)</th><td>Paita (Grande Terre)</td><td>Martens et al. (2019)</td></tr><tr><th colspan="3">Subfamily Eucypridinae Bronstein, 1947</th></tr><tr><th>(?) Eucypris wolffhugeli Méhes, 1914</th><td>Loyalty Isl., Ovéa</td><td>Méhes (1939)</td></tr><tr><th colspan="3">Subfamily Cypridopsinae Kaufmann, 1900</th></tr><tr><th>(?) Cypridopsis sarasini Méhes, 1939</th><td>Loyalty Isl., Ovéa</td><td>Méhes (1939)</td></tr></tbody></table>

FIGURE 5 in A new Potamocypridini genus of Cypridopsinae (Crustacea, Ostracoda) from Thailand, with a discussion on taxonomic characters and morphological evolution in the tribe

FIGURE 5. Neopotamocypris indivisa gen. nov. sp. nov. A. T2 (MSU-ZOC.405). B. T3 (MSU-ZOC.405). C. Terminal part of T3 (MSU-ZOC.405). D. CR (MSU-ZOC.409). E. Female genital hook (MSU-ZOC.409). Scale bars: A–B, D = 50 µm, C, E = 20 µm

FIGURE 2 in A new Potamocypridini genus of Cypridopsinae (Crustacea, Ostracoda) from Thailand, with a discussion on taxonomic characters and morphological evolution in the tribe

FIGURE 2. Neopotamocypris indivisa gen. nov. sp. nov. (MSU-ZOC.409). A. Detail of the posterior part of LVi. B. Detail of the anterior part of LVi. C. Detail of the anterior part of RVi. D. Detail of the posterior part of RVi. Scale bars: A–D = 50 µm.

FIGURE 4 in A new Potamocypridini genus of Cypridopsinae (Crustacea, Ostracoda) from Thailand, with a discussion on taxonomic characters and morphological evolution in the tribe

FIGURE 4. Neopotamocypris indivisa gen. nov. sp. nov. A. Md palp (MSU-ZOC.405). B. Detail of α, β and γ setae (MSUZOC.405). C. Ventral subapical seta, S1 and S2 setae (MSU-ZOC.405). D. Mx1 (MSU-ZOC.405). E. Lateral subapical seta on basal segment of the palp (MSU-ZOC.405). F. Third endite with lateral subapical setae (MSU-ZOC.406). G. T1 (MSUZOC.406). Scale bars: A–F = 20 µm, G = 50 µm.

FIGURE 3 in A new Potamocypridini genus of Cypridopsinae (Crustacea, Ostracoda) from Thailand, with a discussion on taxonomic characters and morphological evolution in the tribe

FIGURE 3. Neopotamocypris indivisa gen. nov. sp. nov. A. A1 (MSU-ZOC.405). B. A2 (MSU-ZOC.405). C. Aesthetasc Y of A2 (MSU-ZOC.405). D. Md coxa (MSU-ZOC.406). E. Rake-like organ ((MSU-ZOC.409). Scale bars: A–B, D = 50 µm, C = 20 µm.

FIGURE 6 in A new Potamocypridini genus of Cypridopsinae (Crustacea, Ostracoda) from Thailand, with a discussion on taxonomic characters and morphological evolution in the tribe

FIGURE 6. Distribution map of Neopotamocypris indivisa gen. nov. sp. nov., numbers see Table 1. (Modified from NordNordWest, Thailand adm location map.svg - https://commons.wikimedia.org/wiki/File:BlankMap-Thailand-provinces. svg)

FIGURE 1 in A new Potamocypridini genus of Cypridopsinae (Crustacea, Ostracoda) from Thailand, with a discussion on taxonomic characters and morphological evolution in the tribe

FIGURE 1. Neopotamocypris indivisa gen. nov. sp. nov. A. CpL from left side (MSU-ZOC.412). B. CpD (MSU-ZOC.411). C. Detail of surface of LVe (MSU-ZOC.412). D. LVi (MSU-ZOC.409). E. RVi (MSU-ZOC.409). F. Detail of muscle scars of RVi (MSU-ZOC.409). Scale bars: A–B, E–F = 100 µm, C = 10 µm, D = 20 µm.