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FIG. 2 in Presence of the foraminifer Chapmanina gassinensis Silvestri, 1931, in the Eocene (Lutetian) of the Grignon "falunière" (Yvelines, Paris Basin). The genus Chapmanina, its species and world distribution

FIG. 2. — The "Falunière" of Grignon section, after Guernet et al. (2012) for the section profile, lithologic units and sub-units and descriptions, Gély (1996) for the sequential units and Huyghe et al. (2012) for the correlation of sequential and lithologic units. Section profile modified from Sanders et al. 2015.

opencc-zeroAug 2018View details →

FIG. 1 in Presence of the foraminifer Chapmanina gassinensis Silvestri, 1931, in the Eocene (Lutetian) of the Grignon "falunière" (Yvelines, Paris Basin). The genus Chapmanina, its species and world distribution

FIG. 1. — Chapmanina gassinensis Silvestri, 1931 (Lutetian, Grignon falunière, Yvelines), in lateral (A) and apical (B) views (MNHN.F.F62410). Scale bars: 200 µm.

Fig. 5 in Benstonea Callm. & Buerki (Pandanaceae): characterization, circumscription, and distribution of a new genus of screw-pines, with a synopsis of accepted species

Fig. 5. – Infructescences and details of stigmas of species of Benstonea Callm. & Buerki. A. Benstonea parva (Ridl.) Callm. & Buerki; B. Benstonea pectinata (Martelli) Callm. & Buerki; C. Benstonea rupestris (. C. Stone) Callm. & Buerki; D. Benstonea thomissophylla (. C. Stone) Callm. & Buerki. [Photos: M. W. Callmander]

Fig. 6 in Benstonea Callm. & Buerki (Pandanaceae): characterization, circumscription, and distribution of a new genus of screw-pines, with a synopsis of accepted species

Fig. 6. – Infructescence of Benstonea thurstonii (C. H. Wright) Callm. & Buerki with details of stigmas in frame. [Photo: M. W. Callmander]

Fig. 2 in Benstonea Callm. & Buerki (Pandanaceae): characterization, circumscription, and distribution of a new genus of screw-pines, with a synopsis of accepted species

Fig. 2. – Plastid maximum likelihood phylogenetic tree of Pandanaceae inferred using RAxML and based on matK, trnL-trnF and trnQ-rps16. Bootstrap support values are represented below branches. This figure is adapted from the figure S1 in BUERKI & al. (2012).

Fig. 1 in Benstonea Callm. & Buerki (Pandanaceae): characterization, circumscription, and distribution of a new genus of screw-pines, with a synopsis of accepted species

Fig. 1. – General habit, infructescences and details of stigmas of species of Pandanus sect. Epiphytica Martelli (A-B) and Pseudoacrostigma B. C. Stone (C-D). A-B. Pandanus epiphyticus Martelli; C. Pandanus platystigma Martelli; D. Pandanus pugnax B. C. Stone. [Photos: M. W. Callmander]

Fig. 3 in Benstonea Callm. & Buerki (Pandanaceae): characterization, circumscription, and distribution of a new genus of screw-pines, with a synopsis of accepted species

Fig. 3. – Distribution map of Benstonea Callm. & Buerki showing the number of species and the level of endemicity per geographical region.

Fig. 22 in The tribe Anthocorini in Japan (Hemiptera: Anthocoridae): descriptions of new species, review of distribution and bionomics

Fig. 22. Distribution of Anthocoris miyamotoi Hiura, 1959 (circles) and A. venustus sp. nov. (triangles) in Japan. Filled symbols represent records based on specimens examined by us, open symbols represent literature records.

Fig. 20 in The tribe Anthocorini in Japan (Hemiptera: Anthocoridae): descriptions of new species, review of distribution and bionomics

Fig. 20. Distribution of Anthocoris chibi Hiura, 1959 (circles) and A. confusus Reuter, 1884 (squares) in Japan. Filled symbols represent records based on specimens examined by us, open symbols represent literature records.

Fig. 21 in The tribe Anthocorini in Japan (Hemiptera: Anthocoridae): descriptions of new species, review of distribution and bionomics

Fig. 21. Distribution of Anthocoris takahashii Hiura, 1959 (circles), A. japonicus Poppius, 1909 (triangles), and A. kalopanacis Kerzhner, 1977 (squares) in Japan. Filled symbols represent records based on specimens examined by us, open symbols represent literature records.

Fig. 18 in The tribe Anthocorini in Japan (Hemiptera: Anthocoridae): descriptions of new species, review of distribution and bionomics

Fig. 18. Distribution of Temnostethus distans Kerzhner, 1973 (circles), T. mirificus sp. nov. (triangles), and Elatophilus nipponensis Hiura, 1966 (squares) in Japan. Filled symbols represent records based on specimens examined by us, open symbols represent literature records.

Fig. 11 in The tribe Anthocorini in Japan (Hemiptera: Anthocoridae): descriptions of new species, review of distribution and bionomics

Fig. 11. Scanning electron micrographs of male genitalia of Anthocoris spp. A–B – A. miyamotoi Hiura, 1959; C–D – A. venustus sp. nov., paratype. A, C – pygophore with paramere, dorsal (A) and lateral (C) views; B, D – paramere, dorsal (B) and lateral (D) views. Abbreviations: prm ‒ paramere; pyg ‒ pygophore.

Fig. 12. Abdominal sterna II in The tribe Anthocorini in Japan (Hemiptera: Anthocoridae): descriptions of new species, review of distribution and bionomics

Fig. 12. Abdominal sterna II–III of Anthocoris spp., male, ventral view (setae omitted). A – A. chibi Hiura, 1959; B – A. confusus Reuter, 1884; C – A. japonicus Poppius, 1909; D – A. nemoralis (Fabricius, 1794); E – A. takahashii Hiura, 1959; F – A. miyamotoi Hiura, 1959; G – A. venustus sp. nov., paratype. Abbreviations: ma ‒ membranous area; st2–3 ‒ abdominal sternum II to III. Scale bars: 0.2 mm.

Fig. 14 in The tribe Anthocorini in Japan (Hemiptera: Anthocoridae): descriptions of new species, review of distribution and bionomics

Fig. 14. Male genitalia of Anthocoris spp. A–C – A. miyamotoi Hiura, 1959; D–F – A. venustus sp. nov., paratype. A, D – pygophore with paramere (ejaculatory bulb omitted), dorsal view; B–C, E–F – paramere, two different views. Abbreviations: prm ‒ paramere; pyg ‒ pygophore. Scale bars: 0.1 mm.

Fig. 17 in The tribe Anthocorini in Japan (Hemiptera: Anthocoridae): descriptions of new species, review of distribution and bionomics

Fig. 17. Habitats, overwintering individuals, and mating pair of Anthocoris spp. A–B – Field survey on hibernating anthocorids under bark-flakes of Zelkova serrata at urbanized zone of Nagasaki City (Kawaguchi Park) in early February; C – A. japonicus Poppius, 1909, overwintering adults under the bark-flake of Z. serrata; D–E – same, mating pair; F – A. miyamotoi Hiura, 1959, adult males and final instar immature (right), overwintering individuals under the bark of Z. serrata; G – same, active male adult on flower of Camellia sasanqua in winter (observed on Jan. 4, 2020).

Fig. 3 in The tribe Anthocorini in Japan (Hemiptera: Anthocoridae): descriptions of new species, review of distribution and bionomics

Fig. 3. Male (A–C, E–G, I–K) and female (D, H, L) genitalia. A–D –Temnostethus distans Kerzhner, 1973; E–H – T. mirificus sp. nov., paratype; I–L – Elatophilus nipponensis Hiura, 1966.A, E, I – pygophore with paramere (ejaculatory bulb omitted), dorsal view; B–C, F–G, J–K – paramere, two different views; D, H, L – copulatory tube and sperm pouch (D, L, sperm pouch broken off), dorsal view. Abbreviations: ct ‒ copulatory tube; prm ‒ paramere; pyg ‒ pygophore; sp ‒ sperm pouch. Scale bars: 0.1 mm.

Fig. 10 in The tribe Anthocorini in Japan (Hemiptera: Anthocoridae): descriptions of new species, review of distribution and bionomics

Fig. 10. Scanning electron micrographs of male genitalia of Anthocoris spp. A–B – A. chibi Hiura, 1959; C–D – A. confusus Reuter, 1884 (from India); E–F – A. japonicus Poppius, 1909. A, C, E – pygophore with paramere, dorsal (A, C) and laterodorsal (E) views; B, D, F – paramere, dorsal (B, D) and laterodorsal (F) views. Abbreviations: end ‒ endosoma; prm ‒ paramere; pyg ‒ pygophore.

Fig. 2 in The tribe Anthocorini in Japan (Hemiptera: Anthocoridae): descriptions of new species, review of distribution and bionomics

Fig. 2. Scanning electron micrographs of diagnostic characters of Japanese anthocorids. A – Temnostethus distans Kerzhner, 1973, female; B, D – T. mirificus sp. nov., female (B) and male (D), paratypes; C – Elatophilus nipponensis Hiura, 1966, female. A–C – ostiolar peritreme and evaporatorium, left lateroventral view; D – pygophore with paramere, lateral view. Abbreviations: eva ‒ evaporatorium; mf ‒ median furrow; op ‒ ostiolar peritreme; prm ‒ paramere; pyg ‒ pygophore.

Fig. 6 in The tribe Anthocorini in Japan (Hemiptera: Anthocoridae): descriptions of new species, review of distribution and bionomics

Fig. 6. Male (A–C, E–G) and female (D, H) genitalia. A–D – Acompocoris brevirostris Kerzhner, 1979; E–H – Tetraphleps aterrima (J. Sahlberg, 1878). A, E – pygophore with paramere (ejaculatory bulb omitted), dorsal view; B–C, F–G – paramere, two different views; D, H – copulatory tube and sperm pouch, dorsal view. Abbreviations: ct ‒ copulatory tube; ism ‒ intersegmental membrane; prm ‒ paramere; pyg ‒ pygophore; sp ‒ sperm pouch. Scale bars: 0.1 mm.

Fig. 9 in The tribe Anthocorini in Japan (Hemiptera: Anthocoridae): descriptions of new species, review of distribution and bionomics

Fig. 9. Scanning electron micrographs of ostiolar peritreme and evaporatorium of Anthocoris spp, left lateroventral view. A – A. chibi Hiura, 1959, female; B – A. confusus Reuter, 1884, male (from India); C – A. japonicus Poppius, 1909, female; D – A. kalopanacis Kerzhner, 1977, female; E – A. takahashii Hiura, 1959, female; F – A. miyamotoi Hiura, 1959, female; G – A. venustus sp. nov., paratype, male. Abbreviations: eva ‒ evaporatorium; mf ‒ median furrow; op ‒ ostiolar peritreme; sca ‒ supracoxal area.