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Figure 3 in Spider diversity in Fanjing Mountain Nature Reserve, Guizhou, China, II: Clubionidae (Araneae)

Figure 3. Clubiona dichotoma Wang, Chen & Zhang ZS, sp. nov. A–B. Habitus, dorsal view. A. Holotype male; B. Paratype female. C–E. Holotype male, left pedipalp. C. Ventral view; D. Retrolateral view; E. Femur, retrolateral view. F–G. Paratype female, epigyne. F. Ventral view; G. Dorsal view. Scale bars: A–B = 1 mm; C–G = 0.2 mm.

Figure 4 in Spider diversity in Fanjing Mountain Nature Reserve, Guizhou, China, II: Clubionidae (Araneae)

Figure 4. Clubiona fanjingshan Wang, Chen & Zhang ZS, sp. nov., holotype male, left pedipalp. A. Ventral view. B. Retrolateral view. Abbreviations: Co—conductor; Em—embolus; RTA—retrolateral tibial apophysis; VTA—ventral tibial apophysis. Scale bars = 0.2 mm.

Figure 1 in Spider diversity in Fanjing Mountain Nature Reserve, Guizhou, China, II: Clubionidae (Araneae)

Figure 1. Clubiona corrugata Bösenberg & Strand, 1906. A–B. Habitus, dorsal view. A. Male; B. Female. C–D. Left male pedipalp. C. Ventral view; D. Retrolateral view. E–F. Epigyne. E. Ventral view; F. Dorsal view. Scale bars: A = 1 mm; B = 2 mm; C–F = 0.2 mm.

Figure S1 in Natural selection on various sites of ribosomal proteins: a cladistic view

Figure S1. Conserved sites of ribosomal protein 40S subunit labeling on crystal structure. The ribbons colored in red represent the synapomorphic s. str. sites of Eukaryota, the green ones represent the synapomorphic s. lat. sites of Eukaryota, and the blue ones represent the potential autapomorphic sites of clades lower than Eukaryota. The magenta ribbons represent the sites related to DBA, and the sites presented by sticks and balls are also synapomorphic sites. Because there are too many synapomorphic sites according to clades lower than Eukaryota in the RP, only the synapomorphic sites related to DBA are colored in this figure (shown in orange).

Figure S2 in Natural selection on various sites of ribosomal proteins: a cladistic view

Figure S2. Conserved sites of ribosomal protein 60S subunit labeling on crystal structure. The ribbons colored in red represent the synapomorphic s. str. sites of Eukaryota, the green ones represent the synapomorphic s. lat. sites of Eukaryota and the blue ones represent the potential autapomorphic sites of clades lower than Eukaryota. The magenta ribbons represent the sites related to DBA, and the sites shown by sticks and balls are also synapomorphic sites. Because there are too many synapomorphic sites according to clades lower than Eukaryota in the RP, only the synapomorphic sites related to DBA are colored in this figure (shown in orange).

Figure 1 in Natural selection on various sites of ribosomal proteins: a cladistic view

Figure 1. Summarized distribution of group-specific sites in the cladogram of eukaryotic diversification. The numerals shown above the line correspond to RPL, and the numerals shown below correspond to RPS. The Ecdysozoa-Neoptera and Chordata-Mammalia lineages are highlighted with blue and yellow, respectively. The amino acids with equivalent biochemical properties were not taken into account.

Figure 2 in Natural selection on various sites of ribosomal proteins: a cladistic view

Figure 2. Conserved sites in the tertiary structures of RPL11 (A) and RPS19 (B). The red ribbons represent the synapomorphic s. str. sites of Eukaryota, the green ones represent the synapomorphic sites s. lat. of Eukaryota, and the blue ones represent the potential autapomorphic sites of clades lower than Eukaryota. The ribbons with sticks and balls represent sites related to DBA. The synapomorphic sites related to DBA are shown in orange. The magenta ones represent the sites for which it is difficult to deduce the synapomorphy but appear to be related to DBA.

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FIG, 1. John William Daly (1933–2008) on the upper Río San Juan. This paper is dedicated to John Daly, our late friend and colleague, who helped collect three of the new species here described. In addition to his globally acclaimed discoveries in chemistry and pharmacology, John was an accomplished field herpetologist who contributed importantly to the systematics and natural history of dendrobatoid frogs (see Grant et al., 2006; Myers, 2009). This photograph shows John at age 37, with the upper Río San Juan behind him and branches overhead of a madroño tree (probably Garcinia magnifolia, syn. Rheedia chocoensis, Clusiaceae). When in South America, John was never far from a dendrobatid frog—this time, in the tree above his head, a tiny, undescribed semiarboreal species (also collected and later named "Dendrobates fuguritus" by our colleague Philip Silverstone). Other dendrobatids found nearby included Phyllobates aurotaenia (Boulenger, 1913), which was then being used for poisoning blowgun darts, and also the nontoxic species that we name Silverstoneia dalyi herein. (Photograph by C. W. Myers, 2 km above Playa de Oro, Chocó, February 16, 1971.) in Review of the Frog Genus Silverstoneia, with Descriptions of Five New Species from the Colombian Chocó (Dendrobatidae: Colostethinae)

FIG, 1. John William Daly (1933–2008) on the upper Río San Juan. This paper is dedicated to John Daly, our late friend and colleague, who helped collect three of the new species here described. In addition to his globally acclaimed discoveries in chemistry and pharmacology, John was an accomplished field herpetologist who contributed importantly to the systematics and natural history of dendrobatoid frogs (see Grant et al., 2006; Myers, 2009). This photograph shows John at age 37, with the upper Río San Juan behind him and branches overhead of a madroño tree (probably Garcinia magnifolia, syn. Rheedia chocoensis, Clusiaceae). When in South America, John was never far from a dendrobatid frog—this time, in the tree above his head, a tiny, undescribed semiarboreal species (also collected and later named "Dendrobates fuguritus" by our colleague Philip Silverstone). Other dendrobatids found nearby included Phyllobates aurotaenia (Boulenger, 1913), which was then being used for poisoning blowgun darts, and also the nontoxic species that we name Silverstoneia dalyi herein. (Photograph by C. W. Myers, 2 km above Playa de Oro, Chocó, February 16, 1971.)

Fig. 3 in Historical, exceptionally large skulls of saltwater crocodiles discovered at the Lee Kong Chian Natural History Museum in Singapore

Fig. 3. Measurement of head length (DCL A and B, see Fig. 2), Inter-Orbital Width (IOW), Maximum Cranial Width (MCW) and Maximum Head Width (MHW) of Edgar, Crocodylus porosus Schneider, 1801.

Fig. 1 in Historical, exceptionally large skulls of saltwater crocodiles discovered at the Lee Kong Chian Natural History Museum in Singapore

Fig. 1. Exceptionally large skulls of Crocodylus porosus Schneider, 1801 discovered at the Lee Kong Chian Natural History Museum (LKCNHM). Edgar on left and Giryu on right.

Fig. 4 in Historical, exceptionally large skulls of saltwater crocodiles discovered at the Lee Kong Chian Natural History Museum in Singapore

Fig. 4. Handwritten date on the mandible of Edgar, Crocodylus porosus Schneider, 1801. It is unknown whether this date refers to a day when the skull was obtained in the field or presented to the museum by Mr. G. Edgar.

Fig. 2 in Historical, exceptionally large skulls of saltwater crocodiles discovered at the Lee Kong Chian Natural History Museum in Singapore

Fig. 2. Measurement of Dorsal Cranial Length (DCL) A and B of Edgar, Crocodylus porosus Schneider, 1801.

Figs. 261–268 in Classification, Natural History, And Evolution Of The Genus Aphelocerus Kirsch (Coleoptera: Cleridae: Clerinae)

Figs. 261–268. Aedeagi, male internal reproductive organs and elytra. 261. Aphelocerus nitidus, aedeagus. 262–263. A. cirritus (262, aedeagus; 263, internal reproductive organs). 264. A. dispilis, aedeagus. 265. A. torosus, aedeagus. 266. A. capillus, internal reproductive organs. 267. A. torosus, elytron. 268. A. acutus, elytron.

Figs. 269–277 in Classification, Natural History, And Evolution Of The Genus Aphelocerus Kirsch (Coleoptera: Cleridae: Clerinae)

Figs. 269–277. Pronota, elytral setal patches, tegmen. 269. Aphelocerus inconstans, pronotum. 270. A. cirritus, pronotum. 271. A. nitidus, elytral setal patches. 272. A. batesi, pronotum. 273. A. bufustis, pronotum. 274. A. cirritus elytral setal patch. 275. A. torosus, pronotum. 276–277. A. olanchoensis (276, pronotum; 277, tegmen).

Figs. 248–255 in Classification, Natural History, And Evolution Of The Genus Aphelocerus Kirsch (Coleoptera: Cleridae: Clerinae)

Figs. 248–255. Pronota, pygidium, sixth visible abdominal sternum, tarsal claws. 248. Aphelocerus. cohibilis, pronotum (dorsal view). 249. A. chondrus (dorsal view). 250. A. improcerus, pronotum (dorsal view). 251. A. protenus, pronotum (dorsal view). 252–253. A. vietus, male (252, pygidium; 253, sixth visible abdominal sternum). 254. A. patulus, female pygidium. 255a. A. leucomelas, tarsal claws. 255b. A. bispineus habitus. 255c. A. ciliaris habitus.

Figs. 241–247 in Classification, Natural History, And Evolution Of The Genus Aphelocerus Kirsch (Coleoptera: Cleridae: Clerinae)

Figs. 241–247. Elytra, habitus, pronota. 241. Aphelocerus coactus, elytra (lateral view). 242. A. immarginatus, elytra (lateral view). 243. A. primigenius, habitus. 244. A. inconstans, habitus. 245. A. panus, pronotum (dorsal view). 246. A. collaris, pronotun (dorsal view). 247. A. hespenheidei, pronotum (dorsal view).

Figs. 193–214. Tegmina and phalli. 193. Aphelocerus delicatulus, tegmen. 194–195. A in Classification, Natural History, And Evolution Of The Genus Aphelocerus Kirsch (Coleoptera: Cleridae: Clerinae)

Figs. 193–214. Tegmina and phalli. 193. Aphelocerus delicatulus, tegmen. 194–195. A. bispineus (194, tegmen; 195, phallus). 196. A. aeneus, tegmen. 197. A. acuticolis, tegmen. 198. A. sculptillus, tegmen. 199. A. sabulosus, tegmen. 200–201. A. akis (200, phallus; 201, tegmen). 202–203. A. chelonus (202, tegmen; 203, phallus). 204. A. scalenus, tegmen. 205. A. ebenus, tegmen. 206. A. hespenheidei, tegmen. 207–208. A. ciliaris (207, tegmen; 208, phallus). 209. A. turnbowi, tegmen. 210. A. improcerus. 211. A. anticus, tegmen. 212. A. inbatus, tegmen. 213. A. chondrus, tegmen. 214. A. monteverde. tegmen.

Fig. 257–260. Elytral vestiture. 257. Aphelocerus leucomelas. 258. A. chiriqui. 259. A. leucomelas. 260. A in Classification, Natural History, And Evolution Of The Genus Aphelocerus Kirsch (Coleoptera: Cleridae: Clerinae)

Fig. 257–260. Elytral vestiture. 257. Aphelocerus leucomelas. 258. A. chiriqui. 259. A. leucomelas. 260. A. ciliaris.

Figs. 184–192. Internal reproductive organs. 184–186. Aphelocerus inconstans. 184–185 in Classification, Natural History, And Evolution Of The Genus Aphelocerus Kirsch (Coleoptera: Cleridae: Clerinae)

Figs. 184–192. Internal reproductive organs. 184–186. Aphelocerus inconstans. 184–185, male (184, accessory glands, testis, and ejaculatory duct; 185, base of medial accessory gland; 186, base of lateral accessory gland). 187–189. A. myrmecoides. 187–188, male (187, accessory glands, testis, and ejaculatory duct; 188, medial accessory gland). 189. Female. 190. A. leucomelas, male. 191. A. discapillus, male. 192. A. cheliferous male.

Figs. 162–183 in Classification, Natural History, And Evolution Of The Genus Aphelocerus Kirsch (Coleoptera: Cleridae: Clerinae)

Figs. 162–183. Aedeagus, habitus, elytral discal setal tufts. 162. Aphelocerus dispilis, aedeagus. 163. Weevil, Myrmex sp. 164. Aphelocerus myrmecoides, 165–183. Elytral discal setal tufts. 165. A. sagittarius. 166. A. triangulus. 167. A. cornuatus. 168. A. humerus. 169. A. acutus. 170. A. lividus. 171. A. protenus. 172. A. argus. 173. A. arenatus. 174. A. catie. 175. A. chiriqui. 176. A. yungas. 177. A. monteverde. 178. A. anticus. 179. A. batesi. 180. A. bufustis. 181. A. acanthus. 182. A. yungas. 183. A. sturnus.