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301 results for “170”
FIGURES 170, 171. Callodicopus floridanus Huber, paratype. 70 in Illustrated key to genera and catalogue of Mymaridae (Hymenoptera) in America north of Mexico
FIGURES 170, 171. Callodicopus floridanus Huber, paratype. 70, head–base of metasoma, lateral; 171, apex of mesosoma + metasoma, lateral showing mesophragma and ovipositor. Scale bars=100 μm.
FIGURES 170–189 in Revision of the genus Bioramix Bates, 1879 (Coleoptera: Tenebrionidae: Platyscelidini) from China
FIGURES 170–189. Parameres of male aedeagus in dorsal and lateral view. 170–171. Bioramix riwoqeica; 172–173. B. rubripes; 174–175. B. rufipalpis; 176–177. B. darbukensis (= B. rufipalpis); 178–179. B. rugelytra; 180–181. B. seidlitzi; 182– 183. B. subcarinata; 184–185. B. tiani; 186–187. B. yushuana; 188–189. B. pamirensis.
FIGS. 170–172. Brunsonia chelanoparva. Fig. 170. Anterior gonopods, posterior view. Fig. 171 in The millipede family Conotylidae in northwestern North America, with a complete bibliography of the family (Diplopoda, Chordeumatida, Heterochordeumatidea, Conotyloidea)
FIGS. 170–172. Brunsonia chelanoparva. Fig. 170. Anterior gonopods, posterior view. Fig. 171. Detail of right anterior gonopod, ventral view. Fig. 172. Right posterior gonopod coxite, posterior view.
finals_2020_11_170
Log and boot files of game 170
FIGURES 163–170 in Taxonomic review of Tipula (Vestiplex Bezzi) crane flies (Diptera: Tipulidae) in Mongolia
FIGURES 163–170. Hypopygium of male T. (Vestiplex) longitudinalis. 163. Tergite 9, dorsal view; 164. Gonocoxite, lateral view; 165. Left outer gonostylus, lateral view; 166. Left inner gonostylus, lateral view; 167. Gonocoxal fragment, dorsal view; 168. Aedeagal guide, lateral view; 169. Sperm pump, dorsal view; 170. Distal part of aedeagus, lateral view. Scale of 163–169 = 0.5 mm, 170 = 0.25 mm.
FIGURE 170 in Generic relationships of New World Jerusalem crickets (Orthoptera: Stenopelmatoidea:Stenopelmatinae), including all known species of Stenopelmatus
FIGURE 170. First drawing of S. talpa to appear in the literature, this from Biologia Centrali-Americana (Saussure & Pictet 1897).
Data from: Rates of dinosaur body mass evolution indicate 170 million years of sustained ecological innovation on the avian stem lineage
Large-scale adaptive radiations might explain the runaway success of a minority of extant vertebrate clades. This hypothesis predicts, among other things, rapid rates of morphological evolution during the early history of major groups, as lineages invade disparate ecological niches. However, few studies of adaptive radiation have included deep time data, so the links between extant diversity and major extinct radiations are unclear. The intensively studied Mesozoic dinosaur record provides a model system for such investigation, representing an ecologically diverse group that dominated terrestrial ecosystems for 170 million years. Furthermore, with 10,000 species, extant dinosaurs (birds) are the most speciose living tetrapod clade. We assembled composite trees of 614–622 Mesozoic dinosaurs/birds, and a comprehensive body mass dataset using the scaling relationship of limb bone robustness. Maximum-likelihood modelling and the node height test reveal rapid evolutionary rates and a predominance of rapid shifts among size classes in early (Triassic) dinosaurs. This indicates an early burst niche-filling pattern and contrasts with previous studies that favoured gradualistic rates. Subsequently, rates declined in most lineages, which rarely exploited new ecological niches. However, feathered maniraptoran dinosaurs (including Mesozoic birds) sustained rapid evolution from at least the Middle Jurassic, suggesting that these taxa evaded the effects of niche saturation. This indicates that a long evolutionary history of continuing ecological innovation paved the way for a second great radiation of dinosaurs, in birds. We therefore demonstrate links between the predominantly extinct deep time adaptive radiation of non-avian dinosaurs and the phenomenal diversification of birds, via continuing rapid rates of evolution along the phylogenetic stem lineage. This raises the possibility that the uneven distribution of biodiversity results not just from large-scale extrapolation of the process of adaptive radiation in a few extant clades, but also from the maintenance of evolvability on vast time scales across the history of life, in key lineages.
FIGURES 158–170 in Review of Empoasca (Distantasca) Dworakowska (Hemiptera: Cicadellidae: Typhlocybinae: Empoascini), with description of two new species from China
FIGURES 158–170. Heads and thoraxes, dorsal view. 158, Empoasca (Distantasca) terminalis Distant, 1918; 159, Empoasca (Distantasca) faciata (Dworakowska, 1972); 160, Empoasca (Distantasca) riora Dworakowska, 1977; 161, Empoasca (Distantasca) tna Dworakowska, 1980; 162, Empoasca (Distantasca) latava Dworakowska, 1981; 163, Empoasca (Distantasca) rokasa Dworakowska, 1981; 164, Empoasca (Distantasca) atika Dworakowska, 1982; 165, Empoasca (Distantasca) tiaca Dworakowska, 1994; 166, Empoasca (Distantasca) bulbosa Dworakowska, 1994; 167, Empoasca (Distantasca) paraterminalis Qin & Zhang; 168, Empoasca (Distantasca) serratipenis Qin & Zhang; 169, Empoasca (Distantasca) tuberculata Zhang & Liu sp. n.; 170, Empoasca (Distantasca) latibasis Zhang & Liu sp. n.
FIGURES 164–170. Female genitalia. 164. Odontodes aleuca. 165. Lophoptera anthyalus. 166 in A taxonomic revision of the Stictopterinae (Lepidoptera, Noctuoidea, Noctuidae) in China
FIGURES 164–170. Female genitalia. 164. Odontodes aleuca. 165. Lophoptera anthyalus. 166. Lophoptera hamata sp. nov. 167. Lophoptera coangulata. 168. Lophoptera stipata. 169. Lophoptera nama. 170. Lophoptera brunnama. Scale bars = 1 mm.
FIGURES 170–174. Chimarra obscurella Banks, 1924, holotype. 170 in Revision of the Fijian Chimarra (Trichoptera, Philopotamidae) with description of 24 new species
FIGURES 170–174. Chimarra obscurella Banks, 1924, holotype. 170—genitalia, left lateral view; 171—genitalia, dorsal view; 172—genitalia, ventral view; 173—phallic apparatus, left lateral view; 174—phallic apparatus, ventral view.
FIGURES 159–170 in Revision of Chinese Oretinae (Lepidoptera, Drepanidae)
FIGURES 159–170. Female genitalia of Oretinae (Scale bar =1 mm). 159, Oreta vatama acutula; 160, O. andrema; 161, O. obtusa dejeani; 162, O. speciosa; 163, O. loochooana loochooana; 164, O. loochooana timutia; 165, O. turpis; 166, O. hoenei hoenei; 167, O. hoenei inangulata; 168, O. paki; 169, O. trispina; 170, O. pavaca pavaca (Paratype of O. zigzaga).
FIGURES 169–170 in A revision of the species of the pseudoscorpion subgenus Chthonius (Ephippiochthonius) (Arachnida, Pseudoscorpiones, Chthoniidae) from Italy and neighbouring areas
FIGURES 169–170. Chthonius (E.) nanus Beier, 1953 (Liguria, Isola di Rovegno). 169, male, right chela, lateral view; 170, female, id. (Scale bar 0.1 mm).
FIGURES 163–170 in A review of the genera Cleigastra Macquart, Gonarcticus Becker, Gonatherus Rondani, Hexamitocera Becker, Nanna Strobl, Orthacheta Becker and Spathephilus Becker (Diptera, Scathophagidae) of Russia
FIGURES 163–170. Nanna tibiella (Zetterstedt) (163–165) and Orthacheta cornuta (Loew) (166–170): 163—end of female abdomen, ventral view; 164—same, dorsal view; 165—same, lateral view; 166—male sternite 5; 167—epandrium, cerci and surstyli, lateral view; 168—same, dorsal view; 169—male sternite 4; 170—distribution map.
FIGURES 165–170 in Review of the Blastobasinae of Costa Rica (Lepidoptera: Gelechioidea: Blastobasidae)
FIGURES 165–170. Male genitalia of Blastobasinae. 165–166, Hypatopa dolo (slide 2136). 167–168, Hypatopa cyane (slide 2398). 169–170, Hypatopa manus (slide 2566).
FIGURES 170–178. Opeatocerata stubbsi Smith, 1989 in Revision of Opeatocerata Melander, 1928 (Diptera: Empididae: Empidinae)
FIGURES 170–178. Opeatocerata stubbsi Smith, 1989, holotype ♂. 170. habitus, lateral view; 171. wing; 172. tergite 8 and terminalia, lateral view; 173. tergites 4-8, dorsal view; 174. terminalia; 175. lobes of cerci, dorsal view; 176. descendant plate of anterior cercus, posterior view; 177. subepandrial sclerite and bacilliform sclerite, dorsal view; 178. ejaculatory apodeme, phallus and hypandrium, lateral view.
PLATE 170. Syntomodrillia hesperia, new species. Figs. 1–3 in Taxonomic review of tropical western Atlantic shallow water Drilliidae (Mollusca: Gastropoda: Conoidea) including descriptions of 100 new species
PLATE 170. Syntomodrillia hesperia, new species. Figs. 1–3: holotype, Tambor Cay, Panama (USNM 1291369). Fig. 1: ventral, lateral & dorsal views; Fig. 2: enlarged view of protoconch (not to scale); Fig. 3: apical view, V = varix, L = edge of outer lip. Figs. 4–7: paratypes, all ventral views. Fig. 4: off Escudo de Veraguas I., (P. Stahlschmidt coll.); Fig. 5: off Escudo de Veraguas I., (ANSP 464997); Fig. 6: off Panama (ANSP 464962); Fig. 7: off Roatan I., Honduras (ANSP 464961).
FIGURES 167–170 in Diversity of Scydmaeninae (Coleoptera: Staphylinidae) in Upper Eocene Rovno amber
FIGURES 167–170.?Rovnoscydmus sp. specimen 2 (K-8971). Laterodorsal (167, 169) and ventrolateral (168, 170) views.
FIGURES 170–177 in Notes on the genus Ceruchus MacLeay from China, with the description of a new species (Coleoptera: Scarabaeoidea: Lucanidae)
FIGURES 170–177. Male genitalia of Ceruchus niger, Yunshanping, Yulongxueshan, Yunnan (same specimen as Fig. 245). 170 — Ninth abdominal segment in ventral view; 171 — Ninth abdominal segment in dorsal view; 172 —whole genitalia in ventral view with penis removed; 173 — whole genitalia in dorsal view with penis removed; 174 — whole genitalia in lateral view with penis removed; 175 — penis detached in lateral view; 176 — penis detached in lateral view; 177 — penis detached in dorsal view. Scale bar 1 mm for all.
FIGURE 170 in The Caucasus as a major hotspot of biodiversity: Evidence from the millipede family Anthroleucosomatidae (Diplopoda, Chordeumatida)
FIGURE 170. Distribution of the Caucasian Anthroleucosomatidae: the Dentatosoma, the Herculina, the Ratcheuma and the Vegrandosoma complexes.
FIGURES 166–170 in Taxonomy and molecular phylogeny of the Platystictidae of Sri Lanka (Insecta: Odonata)
FIGURES 166–170. Coloration in life: Platysticta apicalis—(166) male; (167) female; Platysticta maculata—(168) male; (169) female; Platysticta secreta sp. nov.—(170) male [photos: M. Bedjanič].
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.