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Fig. 21 in Revision of Phoenicocoris Reuter with Descriptions of Three New Species from North America and a New Genus from Japan (Heteroptera: Miridae: Phylinae)

Fig. 21. Scanning electron micrographs of Phoenicocoris dissimilis (Reuter), Huntsville, Pennsylvania (A–C) and Semium subglaber Knight, Tucson, Arizona (D). A. Hind femora, dorsodistal view. B. Pretarsus, apical view. C. Pretarsus, lateral view. D. Pretarsus, apical view. Scales as indicated.

Fig. 8 in Revision of Phoenicocoris Reuter with Descriptions of Three New Species from North America and a New Genus from Japan (Heteroptera: Miridae: Phylinae)

Fig. 8. Scanning electron micrographs of Phoenicocoris australis (Blatchley), Columbia Co., Florida. A. Scalelike setae, dorsal view. B. Hind femora, dorsodistal view. C. Pretarsus, lateral view. Scales as indicated.

Fig. 14 in Revision of Phoenicocoris Reuter with Descriptions of Three New Species from North America and a New Genus from Japan (Heteroptera: Miridae: Phylinae)

Fig. 14. Scanning electron micrographs of Phoenicocoris nevadensis, n.sp., Carroll Summit, Nevada. A. Head and thorax, lateral view. B. Scalelike setae, dorsal view. C. Hind femora, dorsodistal view. D. Pretarsus, apical view. Scales as indicated.

Fig. 12 in Revision of Phoenicocoris Reuter with Descriptions of Three New Species from North America and a New Genus from Japan (Heteroptera: Miridae: Phylinae)

Fig. 12. Scanning electron micrographs of Phoenicocoris minusculus (Knight), Huyck Preserve, New York. A. Head and thorax, lateral view. B. Scalelike setae, dorsal view. C. Pretarsus, ventral view. D. Hind femora, dorsodistal view.

Text-fig. 4. Neogene generic diversity in rodents for the three study areas separately and combined. in Generically Speaking, A Survey On Neogene Rodent Diversity At The Genus Level In The Now Database

Text-fig. 4. Neogene generic diversity in rodents for the three study areas separately and combined.

Text-fig. 3 Ternary diagram of the relative abundance (in %) of juvenile, prime adult, and old adult specimens in samples of Castor fiber (data from Table 3). The red dots indicate the Pleistocene samples of Bilzingsleben II (B), Weimar- Ehringsdorf (E), and Weimar-Taubach (T), the black dot represents an extant population from Telemark in Norway (data from Campbell 2009). Abbreviations of zones (after Discamps and Costamagno 2015): JOP – Juveniles-Old-Prime dominated zone, JPO – Juveniles-Prime-Old dominated zone, O – Old dominated zone, P – Prime dominated zone. The diagram shows the position of all three fossil samples in the prime dominated zone. in Mortality Profiles Of Castor And Trogontherium (Mammalia: Rodentia, Castoridae), With Notes On The Site Formation Of The Mid-Pleistocene Hominin Locality Bilzingsleben Ii (Thuringia, Central Germany)

Text-fig. 3 Ternary diagram of the relative abundance (in %) of juvenile, prime adult, and old adult specimens in samples of Castor fiber (data from Table 3). The red dots indicate the Pleistocene samples of Bilzingsleben II (B), Weimar- Ehringsdorf (E), and Weimar-Taubach (T), the black dot represents an extant population from Telemark in Norway (data from Campbell 2009). Abbreviations of zones (after Discamps and Costamagno 2015): JOP – Juveniles-Old-Prime dominated zone, JPO – Juveniles-Prime-Old dominated zone, O – Old dominated zone, P – Prime dominated zone. The diagram shows the position of all three fossil samples in the prime dominated zone.

Text-fig. 5. Macroevolutionary trends related to the IC model in the first three teeth of the six families of extinct sloths, as well as specimens of the "basal Megatherioidea", Pseudoglyptodon, and Bradypus. Dashed line (- -) shows the regression including all data; solid line shows the regression after the exclusion of Octodontotherium (shown in the plot as a filled triangle). in Unexpected Inhibitory Cascade In The Molariforms Of Sloths (Folivora, Xenarthra): A Case Study In Xenarthrans Honouring Gerhard Storch'S Open-Mindedness

Text-fig. 5. Macroevolutionary trends related to the IC model in the first three teeth of the six families of extinct sloths, as well as specimens of the "basal Megatherioidea", Pseudoglyptodon, and Bradypus. Dashed line (- -) shows the regression including all data; solid line shows the regression after the exclusion of Octodontotherium (shown in the plot as a filled triangle).

Text-fig. 4. Macroevolutionary trends related to the IC model in the last three teeth of the six families of extinct sloths, as well as specimens of the "basal Megatherioidea", Pseudoglyptodon, and Bradypus. Dash-dot line (-.-) shows the regression including all data; solid line shows the regression after the exclusion of Octodontotherium (shown in the plot as a filled triangle). in Unexpected Inhibitory Cascade In The Molariforms Of Sloths (Folivora, Xenarthra): A Case Study In Xenarthrans Honouring Gerhard Storch'S Open-Mindedness

Text-fig. 4. Macroevolutionary trends related to the IC model in the last three teeth of the six families of extinct sloths, as well as specimens of the "basal Megatherioidea", Pseudoglyptodon, and Bradypus. Dash-dot line (-.-) shows the regression including all data; solid line shows the regression after the exclusion of Octodontotherium (shown in the plot as a filled triangle).

Fig. 49 in Phylogeny, Taxonomic Revision, And Character Evolution Of The Genera Chiasmocleis And Syncope (Anura, Microhylidae) In Amazonia, With Descriptions Of Three New Species

Fig. 49. Optimization of absence (gray) and presence (black) of dermal spines (A, three steps) and of the amount of webbing in males (B, four steps) of Chiasmocleis. Optimizations of both characters required three and four steps, respectively for dermal spines and amount of webbing. Presence of spines is the plesiomorphic state, and they were lost three times independently, while the absence of webbing is the plesiomorphic state and it appears four times independently. Taxonomy updated to the one proposed in the present work. Chiasmocleis devriesi is nested within C. anatipes and is not shown.

Fig. 50 in Phylogeny, Taxonomic Revision, And Character Evolution Of The Genera Chiasmocleis And Syncope (Anura, Microhylidae) In Amazonia, With Descriptions Of Three New Species

Fig. 50. Optimization of absence (gray) and presence (black) of the femoral line in Chiasmocleis. Four equally parsimonious alternative explanations, with four steps each. Scenario (A) shows a single appearance of the femoral line, with three reversals; scenarios (B) and (C) depicts alternative scenarios, involving appearances and reversals to absence; scenario (D) postulates four independent appearances of the femoral line. Taxonomy updated to the one proposed in the present work. Chiasmocleis devriesi is nested within C. anatipes and is not shown.

Fig. 48 in Phylogeny, Taxonomic Revision, And Character Evolution Of The Genera Chiasmocleis And Syncope (Anura, Microhylidae) In Amazonia, With Descriptions Of Three New Species

Fig. 48. Advertisement call of Chiasmocleis royi. (A) Oscillogram and (B) spectrogram of a series of nine consecutive notes emitted by a calling male from the type locality, at Tambopata, Madre de Dios, Peru; recorded on 12 December 1990, at 23.4° C air temperature (USNM 343268, paratype; recorded by R.B. Cocroft; recording number USNM tape 269, cut 13).

Fig. 46 in Phylogeny, Taxonomic Revision, And Character Evolution Of The Genera Chiasmocleis And Syncope (Anura, Microhylidae) In Amazonia, With Descriptions Of Three New Species

Fig. 46. Holotype of Chiasmocleis royi, sp. nov. (USNM 343266), in (A) dorsal and (B) ventral views. SVL 5 20.6 mm.

Fig. 45 in Phylogeny, Taxonomic Revision, And Character Evolution Of The Genera Chiasmocleis And Syncope (Anura, Microhylidae) In Amazonia, With Descriptions Of Three New Species

Fig. 45. Holotype of Chiasmocleis papachibe, sp. nov. (MPEG 30683), in (A) dorsal and (B) ventral views. SVL 5 24.8 mm.

Fig. 44 in Phylogeny, Taxonomic Revision, And Character Evolution Of The Genera Chiasmocleis And Syncope (Anura, Microhylidae) In Amazonia, With Descriptions Of Three New Species

Fig. 44. Advertisement call of Chiasmocleis haddadi. (A) Oscillogram and (B) spectrogram of two consecutive multipulsed notes. Recorded at the type locality, Montagne Kotika, French Guiana (recording number FNJV 30718).

Fig. 47 in Phylogeny, Taxonomic Revision, And Character Evolution Of The Genera Chiasmocleis And Syncope (Anura, Microhylidae) In Amazonia, With Descriptions Of Three New Species

Fig. 47. Variation of ventral color pattern in Chiasmocleis royi, sp. nov. (A) Male, from Parque Ambiental Chico Mendes, Rio Branco, Acre, Brazil (UFAC-RB 3539). (B) Male, paratype, from Puerto Maldonado, Madre de Dios, Peru (USNM 343268, paratype). (C–D) Females, Guajará-Mirim, Rondônia, Brazil (CHUNB 23547, 25555, respectively).

Fig. 42 in Phylogeny, Taxonomic Revision, And Character Evolution Of The Genera Chiasmocleis And Syncope (Anura, Microhylidae) In Amazonia, With Descriptions Of Three New Species

Fig. 42. Holotype of Chiasmocleis haddadi, sp. nov. (MNHNP 2011.0139), in (A) dorsal and (B) ventral views. SVL 5 14.4 mm.

Fig. 41 in Phylogeny, Taxonomic Revision, And Character Evolution Of The Genera Chiasmocleis And Syncope (Anura, Microhylidae) In Amazonia, With Descriptions Of Three New Species

Fig. 41. Distribution of Chiasmocleis ventrimaculata and C. royi. Crosses 5 examined specimens of C. ventrimaculata. Dashed area refers to the extension of the Río Pastaza (5 Pastaza River), inside the territory of Ecuador, given as the type locality of C. ventrimaculata by Andersson (1945). Star 5 type locality of C. royi; circles 5 additional examined specimens of C. royi.

Fig. 40 in Phylogeny, Taxonomic Revision, And Character Evolution Of The Genera Chiasmocleis And Syncope (Anura, Microhylidae) In Amazonia, With Descriptions Of Three New Species

Fig. 40. Variation of ventral color pattern in Chiasmocleis ventrimaculata. (A) Cantadera Tacaná, Letícia, Colombia (ICN 50245). (B) Reserva Extrativista do Alto Juruá, Cruzeiro do Sul, Acre, Brazil (UFAC RB 2252). (C–D) Reserva Extrativista Riozinho da Liberdade, Tarauacá, Acre, Brazil (UFACF 641, and UFACF 910, respectively).

Fig. 36 in Phylogeny, Taxonomic Revision, And Character Evolution Of The Genera Chiasmocleis And Syncope (Anura, Microhylidae) In Amazonia, With Descriptions Of Three New Species

Fig. 36. Distribution of Chiasmocleis supercilialba. Star 5 type locality; circle 5 additional specimens examined; cross 5 specimens from Rondônia, Brazil, tentatively labeled as C. cf. supercilialba.

Fig. 35 in Phylogeny, Taxonomic Revision, And Character Evolution Of The Genera Chiasmocleis And Syncope (Anura, Microhylidae) In Amazonia, With Descriptions Of Three New Species

Fig. 35. Paratype of Chiasmocleis supercilialba Morales and McDiarmid, 2009 (USNM 342862), paratype in (A) dorsal, and (B) ventral views. SVL 5 18.8 mm.