Find research datasets worth reusing

Fig. 1 in A new tribe of Tropiduchidae (Hemiptera: Fulgoroidea) with revision of the genus Buca and description of asymmetric hind leg spinulation

Fig. 1. Evolution of the classification of genus Buca Walker, 1858 within Fulgoroidea since its first description.

Figs. 9 and 10. Male terminalia and genitalia. Fig. 9 in A new tribe of Tropiduchidae (Hemiptera: Fulgoroidea) with revision of the genus Buca and description of asymmetric hind leg spinulation

Figs. 9 and 10. Male terminalia and genitalia. Fig. 9. Male terminalia of Buca simplex Walker (Bolivia); A) terminalia, right lateral view (styli removed); B) dorsal view of anal tube and paraproct (distal margin downward); C) lef gonostylus (hind margin upward); D) detail view of gonostylus capitulum (in dorsal view). Fig. 10. Buca asymmetrospinata sp. nov. male genitalia (paratype); A) terminalia, right lateral view (styli removed); B) distal portion of phallus, ventral view; C) dorsal view of anal tube and paraproct (hind margin right); D) lef gonostylus (hind margin upward); E) detail view of gonostylus capitulum (in dorsal view).

Fig. 2 in A new tribe of Tropiduchidae (Hemiptera: Fulgoroidea) with revision of the genus Buca and description of asymmetric hind leg spinulation

Fig. 2. Buca simplex Walker (holotype); A) habitus, right lateral view; B) hind wing and abdomen, lef lateral view; C) metope and clypeus, frontal view; D) head and thorax, dorsal view.

Fig. 4 in A new tribe of Tropiduchidae (Hemiptera: Fulgoroidea) with revision of the genus Buca and description of asymmetric hind leg spinulation

Fig. 4. Buca asymmetrospinata sp. nov. (paratypes, Onkone Gare); A) metope and clypeus, frontal view; B) head and thorax, dorsal view; C) female genitalia in situ, ventral view; D) male genitalia in situ, ventral view.

Fig. 1. Larva I in A key to some Frankliniella (Thysanoptera: Thripidae) larvae found in Florida with descriptions of the first instar of select species

Fig. 1. Larva I of F. kelliae: dorsal setae pairs, D1–D6 of pronotum and D1–D5 of mesonotum (A); arrow indicates small sclerotized teeth between D1 setae of abdominal tergite IX (B); scale = 25 µm.

opencc-by-4.0Dec 2016View details →

Figs. 1–8 in Parasitoids (Hymenoptera: Chalcidoidea) of Toumeyella scales (Hemiptera: Coccidae) in the New World, with description of a new species from Mexico

Figs. 1–8. Coccophagus funiculatus, sp. nov., female. 1, Lateral view of body; 2, mesoscutum, dorsal view; 3, mandible; 4, antenna; 5, stigmal and postmarginal veins; 6, mid-tarsus and mid-tibial spur; 7, antenna with sensilla; 8, 1st funicular segment.

Figs. 15–19 in A detailed updated description of the morphology of the larva of Reesa vespulae (Coleoptera: Dermestidae: Megatominae: Megatomini)

Figs. 15–19. Mature larva of Reesa vespulae (Milliron): 15, pronotum (dorsal, right half; large circles represent points of insertion of large spicisetae, small circles represent points of insertion of hastisetae); 16, right foreleg (dorsal); 17, abdominal tergum I (dorsal, right half; large circles represent points of insertion of large spicisetae, small circles represent points of insertion of hastisetae); 18, abdominal tergum VII (dorsal, right half); 19, abdominal tergum VIII (dorsal, right half). Scale bar = 0.1 mm.

Figs. 4–14 in A detailed updated description of the morphology of the larva of Reesa vespulae (Coleoptera: Dermestidae: Megatominae: Megatomini)

Figs. 4–14. Mature larva of Reesa vespulae (Milliron): 4, antenna (dorso-fronto-lateral); 5, spiciseta; 6, hastiseta; 7, right mandible (dorsal); 8, mandible (latero- ventral); 9, epipharynx (ventral); 10, lacinia (dorsal); 11, lacinia (ventral); 12, maxilla (ventral); 13, labium (ventral); 14, labial palp (ventral). Scale bar = 0.1 mm.

Figs. 1–3 in A detailed updated description of the morphology of the larva of Reesa vespulae (Coleoptera: Dermestidae: Megatominae: Megatomini)

Figs. 1–3. Mature larva of Reesa vespulae (Milliron): 1, dorsal view; 2, lateral view; 3, ventral view. Scale bar = 1.0 mm.

Fig. 41 in Molecular phylogeny of Acerentomidae (Protura), with description of Acerentuloides bernardi sp. nov. from North America

Fig. 41. Molecular phylogeny of Acerentomidae inferred from concatenated COI, 18S rRNA, 28S rDNA D1–D2, and 28S rDNA D3–D6 sequences with maximum likelihood (ML). ML bootstrap values shown above the branches.

Figs. 11–15 in Molecular phylogeny of Acerentomidae (Protura), with description of Acerentuloides bernardi sp. nov. from North America

Figs. 11–15. Acerentuloides bernardi sp. nov. 11. Pronotum and mesonotum, right side; 12. lateral part of metanotum; 13. anterior part of prosternum; 14. anterolateral part of mesosternum; 15. anterolateral part of metasternum. Arrows indicate pores (al = tergal anterolateral, sl = tergal sublateral). Scale bars: 20 µm.

Figs. 1–10 in Molecular phylogeny of Acerentomidae (Protura), with description of Acerentuloides bernardi sp. nov. from North America

Figs. 1–10. Acerentuloides bernardi sp. nov. 1. Head, right side; 2. pseudoculus with seta l3; 3. cephalic seta sd5; 4. maxillary palpus; 5. labial palpus; 6. maxillary gland; 7. comb; 8. female squama genitalis; 9. foretarsus, exterior view; 10. foretarsus, interior view. Arrows indicate pores (cp = clypeal pore, fr = frontal pore). Scale bars: 20 µm.

Figs. 24–34 in Molecular phylogeny of Acerentomidae (Protura), with description of Acerentuloides bernardi sp. nov. from North America

Figs. 24–34. Acerentuloides bernardi sp. nov. scanning electron microscopy photographs. 24. Habitus; 25. labial palp (apical tuf with 4 setae broken; s = labial sensillum); 26. foretarsus, interior view: sensilla t1, t3 and a'; 27. modified seta P2a on mesonotum; 28. modified seta A2 on prosternum; 29. modified seta M2 on prosternum; 30. modified seta A5 on tergite I and P1a on sternite I; 31. abdominal leg on segment III (sa = subapical, am = apical medial, al = apical lateral setae; apical lateral seta is broken); 32. hind margin of sternite VI; 33. hind margin of sternite VII; 34. sternites VIII–XII. Scale bars = 300 µm (Fig. 24), 4 µm (Figs. 25 and 27–29), 10 µm (Fig. 31), and 20 µm (Figs. 26, 30, and 32–34).

Figs. 35–40 in Molecular phylogeny of Acerentomidae (Protura), with description of Acerentuloides bernardi sp. nov. from North America

Figs. 35–40. Acerentulus confinis (Berlese, 1908), American specimen scanning electron microscopy photographs. 35. Habitus; 36. pseudoculus and cephalic setae sd4 and l3; 37. foretarsus, exterior view: sensilla t1, t3 and a'; 38. labial palpi with apical tuf of setae and basal sensillum (s); 39. sternite VIII; 40. modified seta P4 on metanotum. Scale bars = 300 µm (Fig. 35), 20 µm (Figs. 36 and 38), and 40 µm (Figs. 37, 39, and 40).

Figs. 16–23 in Molecular phylogeny of Acerentomidae (Protura), with description of Acerentuloides bernardi sp. nov. from North America

Figs. 16–23. Acerentuloides bernardi sp. nov. 16. Tergite I, right side; 17. tergite VI, right part; 18. tergite VII, right part; 19. tergite VIII; 20. sternite II; 21. abdominal leg of sternite II; 22. sternite VI; 23. sternites VII–IX. Arrows indicate pores (psm = tergal posterosubmedial, psl = tergal posterosublateral, spsm = sternal posterosubmedial, spm = sternal posteromedial). Scale bars: 20 µm.

Fig. 4 in Unexpected absence of exo-erythrocytic merogony during high gametocytaemia in two species of Haemoproteus (Haemosporida: Haemoproteidae), including description of Haemoproteus angustus n. sp. (lineage hCWT7) and a report of previously unknown residual bodies during in vitro gametogenesis

Fig. 4. Comparison of fully grown gametocytes of Haemoproteus angustus n. sp. (lineage hCWT7) from the blood of Curruca communis (A, B), Haemoproteus sittae (unknown lineage) from the blood of Sittae europaea (C, D) and Haemoproteus dolniki (unknown lineage) from the blood of Fringilla coelebs (E, F). Note: the elongate and markedly attenuated nuclei of infected erythrocytes containing advanced gametocytes of the new species (A, B), which is not the case in other Haemoproteus parasites (C–F). All images are from type specimens of these species. Symbols are the same as in Fig. 2. Giemsa-stained thin blood films. Scale bar = 10 µm.

Fig. 7 in Unexpected absence of exo-erythrocytic merogony during high gametocytaemia in two species of Haemoproteus (Haemosporida: Haemoproteidae), including description of Haemoproteus angustus n. sp. (lineage hCWT7) and a report of previously unknown residual bodies during in vitro gametogenesis

Fig. 7. High gametocytaemia of Haemoproteus palloris (lineage hWW1) from the blood of a willow warbler Phylloscopus trochilus. Note that young gametocytes are absent, and the parasitaemia consists exclusively of mature fully grown macro- and microgametocytes, indicating a synchronous parasite development and probable absence of recent maturation of tissue meronts, which are the only source of merozoites for young gametocyte development during Haemoproteus infections. Triangle arrowhead – macrogametocytes; triangle wide arrowheads – microgametocytes. Long arrows – parasite nuclei. Giemsa-stained preparations. Scale bar = 10 µm.

Fig. 2 in Unexpected absence of exo-erythrocytic merogony during high gametocytaemia in two species of Haemoproteus (Haemosporida: Haemoproteidae), including description of Haemoproteus angustus n. sp. (lineage hCWT7) and a report of previously unknown residual bodies during in vitro gametogenesis

Fig. 2. Gametocytes of Haemoproteus angustus n. sp. (lineage hCWT7) from the blood of its type host, the common whitethroat Curruca communis: A-H – macrogametocytes, I-L – microgametocytes. Note: the markedly attenuated width of infected erythrocytes (D–G) containing advanced gametocytes, compared to uninfected erythrocytes, and the presence of predominantly oval or elongate pigment granules in fully grown gametocytes (F–H, J-L). All images are from the hapantotype. Long arrows – parasite nuclei. Short arrows – vacuoles. Arrowheads – pigment granules. Short simple wide arrow – nucleolus. Long triangle wide arrows – unfilled spaces between erythrocyte nuclei and gametocytes. Giemsa-stained thin blood films. Scale bar = 10 µm.

Fig. 6 in Unexpected absence of exo-erythrocytic merogony during high gametocytaemia in two species of Haemoproteus (Haemosporida: Haemoproteidae), including description of Haemoproteus angustus n. sp. (lineage hCWT7) and a report of previously unknown residual bodies during in vitro gametogenesis

Fig. 6. Bayesian Inference tree (A) based on partial (478 bp) cytb sequences of Haemoproteus angustus n. sp. (lineage hCWT7) and the 20 closest related Haemoproteus lineages. Bayesian posterior probabilities and Maximum Likelihood bootstrap values were indicated above and below nodes, respectively. For each lineage, representative GenBank accession numbers and MalAvi lineage codes (if available) are indicated as well as the most common bird host. The scale bar indicates the expected mean number of substitutions per site according to the model of sequence evolution applied. Images B and C show the Median-Joining DNA haplotype network of partial (478 bp) cytb sequences of H. angustus hCWT7 and the 20 closest related Haemoproteus lineages. The upper image (B) shows the host distribution, and the lower image (C) depicts the geographic distribution according to the United Nations geoscheme. Each circle represents a unique haplotype/lineage. The frequency of each lineage is indicated for all haplotypes with more than one record and roughly corresponds to the size of circles. Bars on branches indicate the number of substitutions between two haplotypes. Small white circles represent median vectors, which are hypothetical (often ancestral or unsampled) sequences required to connect existing haplotypes with maximum parsimony.

Fig. 3 in Unexpected absence of exo-erythrocytic merogony during high gametocytaemia in two species of Haemoproteus (Haemosporida: Haemoproteidae), including description of Haemoproteus angustus n. sp. (lineage hCWT7) and a report of previously unknown residual bodies during in vitro gametogenesis

Fig. 3. Comparison of fully grown gametocytes of Haemoproteus angustus n. sp. (lineage hCWT7) from the blood of Curruca communis (A–D), H. belopolskyi (lineage hHIICT1) from the blood of Hippolais icterina (E–H) as well as H. parabelopolskyi (hSYAT2) (I–L), H. pallidulus (hSYAT3) (M–P), H. homogeneae (hSYAT16) (Q–T) and H. majoris (hWW2) (U–X) from the blood of Sylvia atricapilla. Note: the markedly attenuated gametocytes of the new species (A–D), which are not present in other Haemoproteus parasites (E–X); the fully grown gametocytes of H. belopolskyi (F, H) and H. parabelopolskyi (J, L) are bigger than those of H. angustus n. sp.; the pigment granules are predominantly roundish and small in H. pallidulus (M–P); the fully grown gametocytes are small and do not reach poles of infected erythrocytes in H. homogeneae (R, T); the erythrocyte nuclei are displaced laterally by H. majoris (V, X) – all these feature are not characteristic of H. angustus sp. nov. Symbols are the same as in Fig. 2. Giemsa-stained thin blood films. Scale bar = 10 µm.