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Figures 5–8. Neotropical Eucnemidae. 5 in Descriptions of six new species of false click beetles (Coleoptera: Eucnemidae: Macraulacinae), with new identification keys for one tribe and two genera
Figures 5–8. Neotropical Eucnemidae. 5) Dromaeolus comayaguiensis (SEMC), dorsal habitus. 6) Dromaeolus comayaguiensis (SEMC), ventral habitus. 7) Asiocnemis bicolor (SEMC), dorsal view. 8) Asiocnemis bicolor (SEMC), ventral view. (Scale: 6–7 = 5.0 mm; 8–9 = 1.0 mm.)
Figures 9–14 in Two new species of stag beetles (Coleoptera: Lucanidae) from western Yunnan, China
Figures 9–14. Characters of Himaloaesalus gaoligongshanus n. sp.. 9–11) Holotype, male. 12–14) Paratype, female. 9, 12) Prosternal process in full face. 10, 13) Mentum. 11, 14) Antenna. Figures 15–20. Male genitalia of Himaloaesalus gaoligongshanus n. sp. taken from holotype under same scale. 15) Abdominal segment 9 in ventral view. 16) Aedeagus in left lateral view. 17) Aedeagus in dorsal view. 18) Aedeagus in right lateral view. 19–20) Aedeagus in ventral view on different ground. Figure 21. Female genitalia of Himaloaesalus gaoligongshanus n. sp. taken from paratype (Fig. 4–6). Abbreviations: mo, median oviduct; bc, bursa copulatrix; sd, spermathecal duct; s, spermatheca; sg, spermathecal gland; ag, accessory gland.
Figures 1–6 in Two new species of stag beetles (Coleoptera: Lucanidae) from western Yunnan, China
Figures 1–6. Habitus illustrations of Himaloaesalus gaoligongshanus n. sp. under same scale. 1–3) Holotype, male. 4–6) Paratype, female. 1, 4) Dorsal view. 2, 5) Ventral view; 3, 6) Lateral view. Figures 7–8. Head illustrations of Himaloaesalus gaoligongshanus n. sp. in dorsal view. 7) Paratype, male. 8) Paratype female.
Figures 44–46 in Two new species of stag beetles (Coleoptera: Lucanidae) from western Yunnan, China
Figures 44–46. Habitus illustrations of males under same scale. 44) Dorcus apatani from NE India. 45) Dorcus yongreni n. sp., holotype. 46) Dorcus yongreni n. sp., paratype. Figure 47. Habitus illustration of Dorcus yongreni n. sp., paratype, female. Figures 48–50. Mentum of male. 48) Dorcus apatani from NE India. 49–50) Dorcus yongreni n. sp. Figures 51–52. Aedeagus in ventral view under same scale. 51) Dorcus apatani from NE India. 52) Dorcus yongreni n. sp., holotype. Figures 53–55. Flagellum flattened in full-face view under same scale. 53) Dorcus apatani from NE India. 54–55) Dorcus yongreni n. sp. Red arrows indicating the differences between the two species.
Figures 1–8. 1–4 in Two new Eburiini from Mexico (Coleoptera, Cerambycidae, Cerambycinae)
Figures 1–8. 1–4) Susuacanga boteroi sp. nov., holotype female: 1) Dorsal habitus; 2) Ventral habitus; 3) Lateral habitus; 4) Head, frontal view. 5–8) Eburia (Eburia) girouxae sp. nov., holotype male: 5) Dorsal habitus; 6) Ventral habitus; 7) Lateral habitus; 8) Head, frontal view.
Figures 22–37 in Two new species of stag beetles (Coleoptera: Lucanidae) from western Yunnan, China
Figures 22–37. Aedeagi of Himaloaesalus species in left lateral, dorsal, right lateral and ventral views. 22–25) H. saburoi, specimen from Zhangmu, Tibet. 26–29) H. saburoi, specimen from Zhangmu, Tibet. 30–33) H. himalayicus, specimen from Yadong, Tibet. 34–37) H. satoi, specimen from Daweishan, SE Yunnan. Figures 38–43. Female genitalia of Himaloaesalus species. 38) H. himalayicus, specimen from Yadong, C Tibet. 39) H. saburoi, specimen from Zhangmu, Tibet. 40) H. zhejiangensis, specimen from Wuyishan, Fujian. 41–43) H. satoi. 41) Specimen from Fanjingshan, Guizhou. 42) Specimen from Daozhen, Guizhou. 43) Specimen from Daweishan, SE Yunnan. Abbreviations: mo, median oviduct; bc, bursa copulatrix; sd, spermathecal duct; s, spermatheca; sg, spermathecal gland; ag, accessory gland; se, sclerite at entrance of bursa copulatrix.
Figures 26–29 in Two new Vaejovis C.L. Koch 1836 from highlands of the Sierra Madre Occidental, Durango, Mexico (Scorpiones, Vaejovidae)
Figures 26–29. Vaejovis mcwesti sp. nov., from Hwy 36 near Santiago Papasquiaro, Durango, Mexico. 26) Dorsal aspect, male holotype. 27) Ventral aspect, male holotype. 28) Dorsal aspect, female paratype. 29) Ventral aspect, female paratype.
Figures 16–25 in Two new Vaejovis C.L. Koch 1836 from highlands of the Sierra Madre Occidental, Durango, Mexico (Scorpiones, Vaejovidae)
Figures 16–25. Hemispermatophores of Vaejovis sierrae sp. nov. and V. mcwesti sp. nov. 16–20, Right hemispermatophore of V. sierrae: 16) dorsal surface of hemispermatophore; 17) ectal view of midsection; 18) enlarged view of hooks; 19) ectoventral aspect of capsular disk; 20) ventral surface of hemispermatophore. 21–25, Right hemispermatophore of V. mcwesti: 21) dorsal surface of hemispermatophore; 22) ectal view of midsection; 23) enlarged view of hooks; 24) ectoventral aspect of capsular disk; 25) ventral surface of hemispermatophore.
Figures 6–15 in Two new Vaejovis C.L. Koch 1836 from highlands of the Sierra Madre Occidental, Durango, Mexico (Scorpiones, Vaejovidae)
Figures 6–15. Morphology of Vaejovis sierrae sp. nov., based on male holotype. 6) Lateral view of metasoma and telson. 7) Right pedipalp femur, dorsal. 8) Right pedipalp patella, dorsal. 9) Right pedipalp patella, external. 10) Right pedipalp patella, ventral. 11) Right pedipalp chela, dorsal. 12) Right pedipalp chela, external. 13) Right pedipalp chela, ventral. 14) Apposable dentate margin of chela fixed finger. 15) Apposable dentate margin of chela movable finger.
Figures 2–5 in Two new Vaejovis C.L. Koch 1836 from highlands of the Sierra Madre Occidental, Durango, Mexico (Scorpiones, Vaejovidae)
Figures 2–5. Vaejovis sierrae sp. nov., from near Rancho Las Margaritas, Durango, Mexico. 2) Dorsal aspect, male holotype. 3) Ventral aspect, male holotype. 4) Dorsal aspect, female paratype. 5) Ventral aspect, female paratype.
Figures 30–39 in Two new Vaejovis C.L. Koch 1836 from highlands of the Sierra Madre Occidental, Durango, Mexico (Scorpiones, Vaejovidae)
Figures 30–39. Morphology of Vaejovis mcwesti sp. nov., based on male holotype. 30) Lateral view of metasoma and telson. 31) Right pedipalp femur, dorsal. 32) Right pedipalp patella, dorsal. 33) Right pedipalp patella, external. 34) Right pedipalp patella, ventral. 35) Right pedipalp chela, dorsal. 36) Right pedipalp chela, external. 37) Right pedipalp chela, ventral. 38) Apposable dentate margin of chela fixed finger. 39) Apposable dentate margin of chela movable finger.
Figure 1 in Two new Vaejovis C.L. Koch 1836 from highlands of the Sierra Madre Occidental, Durango, Mexico (Scorpiones, Vaejovidae)
Figure 1. Type localities of species of the mexicanus group of Vaejovis C. L. Koch 1836 from the Sierra Madre Occidental: Vaejovis sierrae sp. nov., V. mcwesti sp. nov., and V. montanus Graham and Bryson 2010.
Figure 3 in A new genus and two new species of Pteroplatini Thomson from Central America (Coleoptera: Cerambycidae)
Figure 3. Map depicting the known range and localities of Nubosoplatus inbio (circles), and Corynellus
Figure 2. Corynellus lampyrimorphus, female. A in A new genus and two new species of Pteroplatini Thomson from Central America (Coleoptera: Cerambycidae)
Figure 2. Corynellus lampyrimorphus, female. A) Dorsal habitus. B) Ventral habitus. C) Lateral habitus.
Figure 1. Nubosoplatus inbio, males. A in A new genus and two new species of Pteroplatini Thomson from Central America (Coleoptera: Cerambycidae)
Figure 1. Nubosoplatus inbio, males. A) Dorsal habitus. B) Ventral habitus. C) Dorsal habitus showing color variation.
Data for: The genetic basis of floral mechanical isolation between two hummingbird-pollinated Neotropical understory herbs
<p>Floral divergence can contribute to reproductive isolation among plant lineages, and thus provides an opportunity to study the genetics of speciation, including the number, effect size, mode of action, and interactions of quantitative trait loci (QTL). Moreover, flowers represent suites of functionally interrelated traits, but it is unclear to what extent the phenotypic integration of the flower is underlain by a shared genetic architecture, which could facilitate or constrain correlated evolution of floral traits. Here, we examine the genetic architecture of floral morphological traits involved in an evolutionary switch from bill to forehead pollen placement between two species of hummingbird-pollinated Neotropical understory herbs that are reproductively isolated by these floral differences. For the majority of traits, we find multiple QTL of relatively small effect spread throughout the genome. We also find substantial colocalization and alignment of effects of QTL underlying different floral traits that function together to promote outcrossing and reduce heterospecific pollen transfer. Our results are consistent with adaptive pleiotropy or linkage of many coadapted genes, either of which could have facilitated a response to correlated selection and helped to stabilize divergent phenotypes in the face of low levels of hybridization. Moreover, our results indicate that floral mechanical isolation can be consistent with an infinitesimal model of adaptation.</p>
Figures 14-18. Snoqualmia idaho, n in Snoqualmia, a new polydesmid milliped genus from the northwestern United States, with a description of two new species (Diplopoda, Polydesmida, Polydesmidae)
Figures 14-18. Snoqualmia idaho, n. sp. 14) Nonporiferous midbody segment, dorsal view. 15) Gonopods, lateral view from left side. 16) Left gonopod, posterioventral view. 17) Gonopods, anterior view. 18) Gonopod pulvillus, lateral view.
Figures 7-8. Snoqualmia snoqualmie, n in Snoqualmia, a new polydesmid milliped genus from the northwestern United States, with a description of two new species (Diplopoda, Polydesmida, Polydesmidae)
Figures 7-8. Snoqualmia snoqualmie, n. sp., gonopods. 7) Oblique lateral view from right side. 8) Lateral view from left side.
Figure 120-129 in Systematic revision of Gonaphodiellus taxa, with description of two new genera and fourteen new species (Coleoptera: Scarabaeidae: Aphodiinae)
Figure 120-129. Gonaphodiopsis pachecoi, new species (Rancho Nuevo, San Cristobal de las Casas, Chiapas, Mexico). 120) Epipharynx. 121-122) Habitus (morphological details and length ideogram). 123-124) Aedeagus (dorsal and lateral view). Gonaphodiopsis teopiscaensis, new species (4 mi. NW Teopisca, Chiapas, Mexico). 125) Epipharynx. 126-127) Habitus (morphological details and length ideogram). 128-129) Aedeagus (dorsal and lateral view).
Figure 78-88 in Systematic revision of Gonaphodiellus taxa, with description of two new genera and fourteen new species (Coleoptera: Scarabaeidae: Aphodiinae)
Figure 78-88. Gonaphodioides columbicus (Harold, 1880) (Oberhalb Bogotá, Colombia). 78) Epipharynx. 79) Right labial palp (dorsal view). 80-81) Habitus (morphological details and length ideogram). 82-83) Aedeagus (dorsal and lateral view). Gonaphodioides newtoni, new species (3 mi. N Tlanchinol, Hidalgo, Mexico). 84) Epipharynx. 85-86) Habitus (morphological details and length ideogram). 87-88) Aedeagus (dorsal and lateral view).
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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.