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113 results for “Form D”
FIGURE. Euphorbia chamaesyce: A) individual (Tuscany, Siena province, Chiusi, arable fields near the lake), B) individual (Tuscany, Arezzo province, Pieve Santo Stefano, gravel road along shores of Montedoglio Lake), C) detail of cyathium and capsule (hairy form), D) detail of tip and capsules (intermediate hairiness form), E) detail of cyathium and capsule (glabrous form). in Synopsis of Euphorbia section Anisophyllum (Euphorbiaceae) in Italy, with an insight on variation of distribution over time in Tuscany
FIGURE. Euphorbia chamaesyce: A) individual (Tuscany, Siena province, Chiusi, arable fields near the lake), B) individual (Tuscany, Arezzo province, Pieve Santo Stefano, gravel road along shores of Montedoglio Lake), C) detail of cyathium and capsule (hairy form), D) detail of tip and capsules (intermediate hairiness form), E) detail of cyathium and capsule (glabrous form).
FIGURE11. Life stages of Platynaspis variegata Crotch: a, b, d–i. larva; c. adult, nominate form; j–m. darker variant (Image credits: Dr Rojeet Thangjam, CAU, Imphal). in A review of Platynaspini (Coleoptera: Coccinellidae) of the Indian subcontinent, including description of a new genus from north-eastern India and Bangladesh
FIGURE11. Life stages of Platynaspis variegata Crotch: a, b, d–i. larva; c. adult, nominate form; j–m. darker variant (Image credits: Dr Rojeet Thangjam, CAU, Imphal).
X-Ray diffraction images from a crystal of WT, full-length D. radiodurans DdrC - Crystal form xMJ7124
<p>Full-length dimer of DNA-Damage Response Protein C from Deinococcus radiodurans. Crystal Form xMJ7124</p>
FIGURE 3. Acianthera kautskyi—A. Habit. B. Flower, lateral view. C. Flower, dorsal view. Acianthera crinita D. Habit. E. Flower, tipical form. F. Flower, dark form. G in Nomenclatural notes in miscellaneous species of Acianthera (Pleurothallidinae, Orchidaceae)
FIGURE 3. Acianthera kautskyi—A. Habit. B. Flower, lateral view. C. Flower, dorsal view. Acianthera crinita D. Habit. E. Flower, tipical form. F. Flower, dark form. G. Flower, alba form. Images by Wade L. Collier (A–E) and Eric C. Smidt (F–G) based in Toscano de Brito, A.L.V. 3640 (UPCB 101716) (A–C), Toscano de Brito, A.L.V. 3560 (UPCB 86955) (D–E) and Klingelfuss, M. sn. (unvouchered) (F–G).
X-Ray diffraction images from a crystal of D. radiodurans DdrC - PDB 7UDI - Crystal form xMJ7121
<p>Dimer of the DNA-Damage Response Protein C (DdrC) from Deinococcus radiodurans. </p><p>Crystal Form xMJ7121. </p><p>FL protein with L131M/184M mutation and derivatized with SeMet. </p><p>Collected at 0.9795 Å</p><p>Rotation about omega. 1120 frames at a width of 0.25°/frame.</p><p>Data collected in two 140° wedges.</p><p>Raw data integrated and scaled in autoPROC. </p>
Ci-contre: Instantanés sur la biologie de quelques Cigales thaïlandaises 1, Cryptotympana aquila (Walker, 1850), mâle en train de s'alimenter (objectif de 100 mm, en cage). – 2, Cryptotympana mandarina Distant, 1891, femelle achevant sa métamorphose (objectif de 135 mm, in natura, 0 h 45). – 3, Meimuna durga (Distant, 1881); mâle cymbalisant, ailes non écartées (objectif de 135 mm, in natura, 14 h 15). – 4, Meimuna durga (Distant, 1881), mâle et femelle accouplés (objectif de 135 mm, in natura, 13 h 45). – 5, Pomponia linearis (Walker, 1850), mâle au repos (objectif de 135 mm, in natura, le matin, vers 11 heures). – 6 et 7, Tanna ventriroseus n. sp., mâle cymbalisant (6); mâle s'alimentant (7); (objectif de 100 mm, en cage). – 8, Terpnosia nonusaprilis n. sp., mâle cymbalisant, ailes non écartées (objectif de 135 mm, in natura). – 9, Terpnosia nonpareil s n. sp., mâle et femelle accouplés (objectif de 300 mm, in natura, 11 h 55). – 10, Meimuna tavoyana (Distant, 1888), mâle; vue des 3/4 ventraux mettant en évidence la forme et l'écartement de ses opercules (objectif de 100 mm, en cage). – 11, Gaeana cheni Chou & Yao, 1985, mâle achevant de se métamorphoser (objectif de 135 mm, in natura, la nuit, 3 h 17). – 12, Gaeana cheni Chou & Yao, 1985, couple venant de chuter à terre (objectif de 135 mm, 14 h 35). – 13, Ambragaeana ambra Chou & Yao, 1985, mâle dans la phase finale de sa métamorphose, achevant de pigmenter sa livrée (objectif de 135 mm, in natura, au milieu d'une matinée ensoleillée). (Photographies Michel Boulard). in Éthologie sonore et statut acoustique de quelques Cigales thaïlandaises, incluant la description de deux espèces nouvelles (Hemiptera : Auchenorhyncha*, Cicadoidea, Cicadidae)
Ci-contre: Instantanés sur la biologie de quelques Cigales thaïlandaises 1, Cryptotympana aquila (Walker, 1850), mâle en train de s'alimenter (objectif de 100 mm, en cage). – 2, Cryptotympana mandarina Distant, 1891, femelle achevant sa métamorphose (objectif de 135 mm, in natura, 0 h 45). – 3, Meimuna durga (Distant, 1881); mâle cymbalisant, ailes non écartées (objectif de 135 mm, in natura, 14 h 15). – 4, Meimuna durga (Distant, 1881), mâle et femelle accouplés (objectif de 135 mm, in natura, 13 h 45). – 5, Pomponia linearis (Walker, 1850), mâle au repos (objectif de 135 mm, in natura, le matin, vers 11 heures). – 6 et 7, Tanna ventriroseus n. sp., mâle cymbalisant (6); mâle s'alimentant (7); (objectif de 100 mm, en cage). – 8, Terpnosia nonusaprilis n. sp., mâle cymbalisant, ailes non écartées (objectif de 135 mm, in natura). – 9, Terpnosia nonpareil s n. sp., mâle et femelle accouplés (objectif de 300 mm, in natura, 11 h 55). – 10, Meimuna tavoyana (Distant, 1888), mâle; vue des 3/4 ventraux mettant en évidence la forme et l'écartement de ses opercules (objectif de 100 mm, en cage). – 11, Gaeana cheni Chou & Yao, 1985, mâle achevant de se métamorphoser (objectif de 135 mm, in natura, la nuit, 3 h 17). – 12, Gaeana cheni Chou & Yao, 1985, couple venant de chuter à terre (objectif de 135 mm, 14 h 35). – 13, Ambragaeana ambra Chou & Yao, 1985, mâle dans la phase finale de sa métamorphose, achevant de pigmenter sa livrée (objectif de 135 mm, in natura, au milieu d'une matinée ensoleillée). (Photographies Michel Boulard).
Plate III. Rhinolophus simpleX group; skulls; front views f, all other figures f. Fig.. Rh. simpleX (p. 76); Lombok; type of the species. Front view. 2 a, b, c. Rh. megaphyllus f. typica (p. 79); Cooktown; B.M. no. 3.8.3.3. Upper, lateral, and front views. 3. Rh. nanus (p. 82); Goram; type. Front view. 4a, b. Rh. celebensis (p. 83); Makassar; type. Upper and front views. 5 a, 6, c. Rh. borneensis f. typica (p. 84); Labuan; topotype; B.M. no. 65.5.9.15. Upper, lateral, and front views. 6. Rh. malayanus (p. 89); Biserat; topotype; B.M. no. 3.2.6.84. Front view. 7 a, b, c. Rh. nereis (p. 90); Siantan, Anambas; type. Upper, lateral, and front views. 8 a, b. Rh. stheno (p. 91); Selangor; topotype; B.M. no. 98.3.13.2. Lateral and front views. 9 a, b, c, d. Rh. rouXi f. typica (p. 93); Ceylon. Upper, lower, lateral, and front views. 10. Rh.thomasi (p. 100); Talio, Karin Hills; topotype; B.M. no. 90.4.7.9. Upper view. 11 a, b. Rh. affinis himalayanus (p. 103); Nepal. Lower and front views. 12. Rh. a. tener (p. 103); Pegu; type. Upper view. 13. Rh. a. princeps (p. 106); Lombok; type. Upper view. in On some Bats of the Genus Rhinolophus, with Remarks on their Mutual Affinities, and Descriptions of Twenty-six new Forms.
Plate III. Rhinolophus simpleX group; skulls; front views f, all other figures f. Fig.. Rh. simpleX (p. 76); Lombok; type of the species. Front view. 2 a, b, c. Rh. megaphyllus f. typica (p. 79); Cooktown; B.M. no. 3.8.3.3. Upper, lateral, and front views. 3. Rh. nanus (p. 82); Goram; type. Front view. 4a, b. Rh. celebensis (p. 83); Makassar; type. Upper and front views. 5 a, 6, c. Rh. borneensis f. typica (p. 84); Labuan; topotype; B.M. no. 65.5.9.15. Upper, lateral, and front views. 6. Rh. malayanus (p. 89); Biserat; topotype; B.M. no. 3.2.6.84. Front view. 7 a, b, c. Rh. nereis (p. 90); Siantan, Anambas; type. Upper, lateral, and front views. 8 a, b. Rh. stheno (p. 91); Selangor; topotype; B.M. no. 98.3.13.2. Lateral and front views. 9 a, b, c, d. Rh. rouXi f. typica (p. 93); Ceylon. Upper, lower, lateral, and front views. 10. Rh.thomasi (p. 100); Talio, Karin Hills; topotype; B.M. no. 90.4.7.9. Upper view. 11 a, b. Rh. affinis himalayanus (p. 103); Nepal. Lower and front views. 12. Rh. a. tener (p. 103); Pegu; type. Upper view. 13. Rh. a. princeps (p. 106); Lombok; type. Upper view.
Side views of nose-leaves, showing the principal forms of the connecting process in the _R7z. simpleX group (a) and the Rh. lepidus group (6, c, d). a. Rh. borneensis typicus\ b. Rh. cornutus pumilus; c. Rh. monoceros; d. Rh. empusa. in On some Bats of the Genus Rhinolophus, with Remarks on their Mutual Affinities, and Descriptions of Twenty-six new Forms.
Side views of nose-leaves, showing the principal forms of the connecting process in the _R7z. simpleX group (a) and the Rh. lepidus group (6, c, d). a. Rh. borneensis typicus\ b. Rh. cornutus pumilus; c. Rh. monoceros; d. Rh. empusa.
Figure 2 from: Haelewaters D, De Kesel A (2020) Checklist of thallus-forming Laboulbeniomycetes from Belgium and the Netherlands, including Hesperomyces halyziae and Laboulbenia quarantenae spp. nov. MycoKeys 71: 23-86. https://doi.org/10.3897/mycokeys.71.53421
Figure 2 Maximum clade creditability tree of Laboulbenia isolates reconstructed from an LSU dataset, with L. bruchii as outgroup. The topology is the result of Bayesian inference performed with BEAST. For each node, ML BS (≥ 65) and Bayesian pp (≥ 0.7) are presented above/below the branch leading to that node. Isolates are color-coded by host; L. quarantenae sp. nov. is highlighted with gray shading.
Figure 1 from: Haelewaters D, De Kesel A (2020) Checklist of thallus-forming Laboulbeniomycetes from Belgium and the Netherlands, including Hesperomyces halyziae and Laboulbenia quarantenae spp. nov. MycoKeys 71: 23-86. https://doi.org/10.3897/mycokeys.71.53421
Figure 1 Maximum clade creditability tree of Hesperomyces isolates reconstructed from an ITS dataset, with H. coleomegillae as outgroup. The topology is the result of Bayesian inference performed with BEAST. For each node, ML BS (≥ 65) and Bayesian pp (≥ 0.7) are presented above/below the branch leading to that node. Hesperomyces virescens sensu lato is highlighted with light gray shading, isolates are color-coded by host; H. virescens sensu stricto and H. halyziae sp. nov. are highlighted with dark gray shading.
Figure 3 from: Haelewaters D, De Kesel A (2020) Checklist of thallus-forming Laboulbeniomycetes from Belgium and the Netherlands, including Hesperomyces halyziae and Laboulbenia quarantenae spp. nov. MycoKeys 71: 23-86. https://doi.org/10.3897/mycokeys.71.53421
Figure 3 Hesperomyces halyziae Haelew. & De Kesel from Halyzia sedecimguttataA mature thallus from slide D. Haelew. 955a, holotype B mature thallus from slide BR5020212156406V. Scale bar: 100 µm.
Figure 4 from: Haelewaters D, De Kesel A (2020) Checklist of thallus-forming Laboulbeniomycetes from Belgium and the Netherlands, including Hesperomyces halyziae and Laboulbenia quarantenae spp. nov. MycoKeys 71: 23-86. https://doi.org/10.3897/mycokeys.71.53421
Figure 4 A–ILaboulbenia quarantena De Kesel & Haelew. from Bembidion biguttatum, specimen ADK6448: A mature thallus from prothorax, slide BR5020212163329V, holotype B mature thallus from prothorax with less pigmented perithecium C mature thallus from the right mesofemur D–F mature thalli from the right protibia G immature thallus from the prothorax H mature thallus from the right mesofemur I ascospores J–K laboulbenia vulgaris Peyr: J mature thallus from prothorax of Bembidion tetracolum, specimen ADK5557 K mature thallus from mesothorax of Ocys harpaloides, specimen ADK6353. One of the diagnostic characteristics of the new species–the positioning of the insertion cell–is shown in a mature thallus of L. quarantenae (E) and one of L. vulgaris (J). Scale bar: 100 µm.
Figure 8 from: Al-Kandari M, Oliver PG, Salvi D (2021) Molecular and morphological systematics of a new, reef forming, cupped oyster from the northern Arabian Gulf: Talonostrea salpinx new species. ZooKeys 1043: 1-20. https://doi.org/10.3897/zookeys.1043.66992
Figure 8 Photographs of Talonostrea salpinx sp. nov. beds and reefs from Al-Bakri et al. 1985A–C reefs and beds in Khor Al-Subiyah D oyster field at Al-Memlahah, south-eastern end of Kuwait Bay.
Figure 7 from: Al-Kandari M, Oliver PG, Salvi D (2021) Molecular and morphological systematics of a new, reef forming, cupped oyster from the northern Arabian Gulf: Talonostrea salpinx new species. ZooKeys 1043: 1-20. https://doi.org/10.3897/zookeys.1043.66992
Figure 7 Anatomy of Talonostrea salpinx sp. nov. A gross view after removal of upper (right) valve B gross view including route of alimentary canal after removal of ctenidia, gonad and digestive diverticula C mantle edge D rectum and anus E excised labial palp F portion of ctenidium showing fine structures. Abbreviation: am, adductor muscle; an, anus; cp, ciliated pad; ct, ctenidium; ct/m, ctenidium mantle edge junction; hg, hind gut; hg loop, hind gut loop behind stomach; imf, inner mantle fold; ljct, longitudinal junction; lp, labial palp; me, mantle edge; mg, mid gut; mmf, middle mantle fold; mt, mantle; oe,oesophagus; og, oral groove; pc, pericardium; r, rectum; rods, ctenidial filaments; s, stomach; ss, style sac; tjct, transverse junction; vm, visceral mass.
Figure 6 from: Al-Kandari M, Oliver PG, Salvi D (2021) Molecular and morphological systematics of a new, reef forming, cupped oyster from the northern Arabian Gulf: Talonostrea salpinx new species. ZooKeys 1043: 1-20. https://doi.org/10.3897/zookeys.1043.66992
Figure 6 Talonostrea salpinx sp. nov. shells from Umm Al-Namil A, B external and internal views of a shell with marginal fluted spines, Paratypes NMW.Z.2021.009.006/ C, D Paratypes, NMW.Z.2021.009.006/2–3, shells of differing colours and lacking marginal fluted spines E clump of shells some with fluted spines associated with the tubeworm Spirobranchus kraussi (Baird, 1864) and the barnacle Amphibalanus amphitrite (Darwin, 1854). F, rock encrusted with irregular shaped shells mostly lacking fluted spines.
Figure 2 from: Al-Kandari M, Oliver PG, Salvi D (2021) Molecular and morphological systematics of a new, reef forming, cupped oyster from the northern Arabian Gulf: Talonostrea salpinx new species. ZooKeys 1043: 1-20. https://doi.org/10.3897/zookeys.1043.66992
Figure 2 Map of Kuwait indicating known distribution of Talonostrea salpinx sp. nov. Blue circle for field records, red diamond for cited material, red square for type locality. Details of localities are given in Table 1.
Figure 5 from: Al-Kandari M, Oliver PG, Salvi D (2021) Molecular and morphological systematics of a new, reef forming, cupped oyster from the northern Arabian Gulf: Talonostrea salpinx new species. ZooKeys 1043: 1-20. https://doi.org/10.3897/zookeys.1043.66992
Figure 5 Talonostrea salpinx sp. nov. Paratypes from Khor Al-Subiyah, NMW.Z.2021.009.005 A, B clump with and without upper valves C in situ photograph of a shell from a sheltered position D small upper valve with an array of trumpet-shaped projections along margin E Inner views of four shells showing variation in shape and internal colouration.
Figure 1 from: Al-Kandari M, Oliver PG, Salvi D (2021) Molecular and morphological systematics of a new, reef forming, cupped oyster from the northern Arabian Gulf: Talonostrea salpinx new species. ZooKeys 1043: 1-20. https://doi.org/10.3897/zookeys.1043.66992
Figure 1 Oyster beds and reefs in northern Kuwait A, B Khor Al-Subiyah C, D Ashairij E, F Boubyan Island (North Khor Al-Subiyah).
Figure 4 from: Al-Kandari M, Oliver PG, Salvi D (2021) Molecular and morphological systematics of a new, reef forming, cupped oyster from the northern Arabian Gulf: Talonostrea salpinx new species. ZooKeys 1043: 1-20. https://doi.org/10.3897/zookeys.1043.66992
Figure 4 Talonostrea salpinx sp. nov. from Ashairij A, B clump with and without upper valves, shell h is holotype C inner views of lower and upper valves of holotype, NMW.Z. 2021.009. 001 D inner views of upper valves of five paratypes showing variation in shape and colouration, NMW.Z.009.002 E upper valve with a trumpet shapes projection, arrowed F a small upper valve showing radial purple-black colour banding.
Figure 3 from: Al-Kandari M, Oliver PG, Salvi D (2021) Molecular and morphological systematics of a new, reef forming, cupped oyster from the northern Arabian Gulf: Talonostrea salpinx new species. ZooKeys 1043: 1-20. https://doi.org/10.3897/zookeys.1043.66992
Figure 3 Bayesian phylogenetic tree based on cox1 and 16S DNA sequence data. Bayesian posterior probability higher than 0.9 are reported in correspondence of the nodes.
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