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256 results for “Locality records”
FIGURES 2–8. 2 in The Braconinae (Hymenoptera: Braconidae) of Turkey, with new locality records and descriptions of two new species of Bracon Fabricius, 1804
FIGURES 2–8. 2—head in frontal view; 3—antenna; 4—mesosoma in lateral view; 5—foerwing; 6—hind wing, 7—hind leg; 8—metasoma. Scale: 1 mm (Fig 2), 0.8 mm (Fig. 4), 1.4 mm (Fig. 3), 1.3 mm (Figs. 5, 6, 7), 1.2 mm (Fig. 8).
FIGURE1. Breeding, migrating and wintering distributions of Palearctic Anthus [rubescens] japonicus and Nearctic Anthus rubescens rubescens/alticola subspecies groups (from BirdLife International 2022; illustration @Andrew Birch). Circles indicate origins of sequenced individuals and triangles indicate origins of analysed recordings of calls. Localities outside of the usual range of the species complex (e.g., Ireland, Oman and Israel) are not figured here. in --Molecular--and--acoustic--evidence--support--the--species--status--of--Anthus rubescens rubescens and--Anthus [rubescens] japonicus--(Passeriformes:--Motacillidae)
FIGURE1. Breeding, migrating and wintering distributions of Palearctic Anthus [rubescens] japonicus and Nearctic Anthus rubescens rubescens/alticola subspecies groups (from BirdLife International 2022; illustration @Andrew Birch). Circles indicate origins of sequenced individuals and triangles indicate origins of analysed recordings of calls. Localities outside of the usual range of the species complex (e.g., Ireland, Oman and Israel) are not figured here.
FIGURE 2. Cryptothele ceylonica O in Redescription and new locality records of Cryptothele ceylonica O. Pickard-Cambridge, 1877 from Sri Lanka (Araneae: Zodariidae)
FIGURE 2. Cryptothele ceylonica O. Pickard-Cambridge, 1877. A. Male right palp, retrolateral; B, epigynum, ventral; C, vulva, ventral view. Abbreviations: C, conductor; E embolus; Lp, lateral pocket; Se, septum. Scale lines = 0.2 mm (A, B), 0.1 mm (C, D).
FIGURE 1. Cryptothele ceylonica O in Redescription and new locality records of Cryptothele ceylonica O. Pickard-Cambridge, 1877 from Sri Lanka (Araneae: Zodariidae)
FIGURE 1. Cryptothele ceylonica O. Pickard-Cambridge, 1877. A–C. Male left palp; D–E. Juvenile holotype female (OUM- NH); F. Male habitus (IFS_Zod_006); G. Female habitus (IFS_Zod_007); A. Prolateral; C. Retrolateral; D, F–G. Dorsal; B, E, H. Ventral. Abbreviations: C, conductor; Cp, cephalic pit; E embolus; Lp, lateral pocket; Se, septum; T, tegulum, Te, tegular extension. Scale lines = 0.2 mm (C, H), 0.5 mm (A, B), 1 mm (F), 2.0 mm (D, G, E).
FIGURES 4‒8. Localities L1 in Rediscovery and redescription of Oxycheila buestani Wiesner with the first female record and new methodology for observation of Oxycheila Dejean and Oxygonia Mannerheim (Coleoptera: Cicindelidae)
FIGURES 4‒8. Localities L1 (Figs 4‒6) and L2 (Figs 7,8). 4, 8: habitat; 5: drinking water construction at L1; 6, 7: window trap instalations.
Characterization of Complex Pulse Shapes in Deep Brain Stimulation for Movement Disorders Using EEG and Local Field Potential Recordings
ClinicalTrials.gov study NCT04658641. IPD Sharing: NO. Countries: 1. Publications: 3.
Data from: Resource specialists lead local insect community turnover associated with temperature – analysis of an 18-year full-seasonal record of moths and beetles
Insect responses to recent climate change are well documented, but the role of resource specialization in determining species vulnerability remains poorly understood. Uncovering local ecological effects of temperature change with high-quality, standardized data provides an important first opportunity for predictions about responses of resource specialists, and long-term time series are essential in revealing these responses. Here, we investigate temperature-related changes in local insect communities, using a sampling site with more than a quarter-million records from two decades (1992–2009) of full-season, quantitative light trapping of 1543 species of moths and beetles. We investigated annual as well as long-term changes in fauna composition, abundance and phenology in a climate-related context using species temperature affinities and local temperature data. Finally, we explored these local changes in the context of dietary specialization. Across both moths and beetles, temperature affinity of specialists increased through net gain of hot-dwelling species and net loss of cold-dwelling species. The climate-related composition of generalists remained constant over time. We observed an increase in species richness of both groups. Furthermore, we observed divergent phenological responses between cold- and hot-dwelling species, advancing and delaying their relative abundance, respectively. Phenological advances were particularly pronounced in cold-adapted specialists. Our results suggest an important role of resource specialization in explaining the compositional and phenological responses of insect communities to local temperature increases. We propose that resource specialists in particular are affected by local temperature increase, leading to the distinct temperature-mediated turnover seen for this group. We suggest that the observed increase in species number could have been facilitated by dissimilar utilization of an expanded growing season by cold- and hot-adapted species, as indicated by their oppositely directed phenological responses. An especially pronounced advancement of cold-adapted specialists suggests that such phenological advances might help minimize further temperature-induced loss of resource specialists. Although limited to a single study site, our results suggest several local changes in the insect fauna in concordance with expected change of larger-scale temperature increases.
Data from: The critical role of local refugia in postglacial colonization of Chinese pine: joint inferences from DNA analyses, pollen records, and species distribution modeling
The importance of long-distance migration from low to high latitudes relative to local spread from northern refugia after the Last Glacial Maximum (LGM) remains a focus of debate for many temperate tree species. We assessed the dynamics of Chinese pine (Pinus tabulaeformis), a widespread species endemic to northern China, since the LGM by integrating cytoplasmic DNA data, mapped pollen records and ecological niche modeling. Genetic variation among 544 individuals from 50 populations spanning the entire natural species range revealed eight genetic clusters with distinct geographic distribution, indicating glacial lineages likely originating from multiple local microrefugia. Palynological evidence suggested that the northernmost part of the natural distribution originated from local postglacial spread. Niche modeling indicated high probability of the species being present in the area of the Loess Plateau and coastal areas north of the Yangtze River during the LGM. The three lines of evidence jointly suggest that the species persisted through the last glaciation in the mountains surrounding the Loess Plateau of northern China and that the current distribution of the species originated primarily from the spread of local refugial populations, instead of long-distance migration. These results cast doubt on the notion that Chinese pine migrated from areas south of the Yangtze River and underscore the importance of northern refugia.
FIGURES 12–13. Anacroneuria singularis adult. 12 in Description of the nymph of Anacroneuria singularis Righi-Cavallaro & Lecci (Plecoptera: Perlidae) and a new locality record for northern Brazil
FIGURES 12–13. Anacroneuria singularis adult. 12. Female; 13. Male (Photos: J.M.F. Ribeiro).
FIGURE 2 in A new species and locality record for Pseudopsyra katydid (Orthoptera: Phaneropterinae)
FIGURE 2. Pseudopsyra taksini sp. nov. male living habitus in profile view.
FIGURE 1 in A new species and locality record for Pseudopsyra katydid (Orthoptera: Phaneropterinae)
FIGURE 1. Distribution of all known species of Pseudopsyra.
Distribution. Recorded only from two localities in S Somalia. in Soricidae
Distribution. Recorded only from two localities in S Somalia.
Figure 6 from: Branch WR, Haacke W, Vaz Pinto P, Conradie W, Baptista N, Verburgt L, Verisimmo L (2017) Loveridge's Angolan geckos, Afroedura karroica bogerti and Pachydactylus scutatus angolensis (Sauria, Gekkonidae): new distribution records, comments on type localities and taxonomic status. Zoosystematics and Evolution 93(1): 157-166. https://doi.org/10.3897/zse.93.10915
Figure 6 - Regional variation in colouration of Pachydactylus angolensis from Angola. A Pachydactylus angolensis – inland form (Serra da Tchivira: photo P. Vaz Pinto) B Pachydactylus angolensis – coastal form (Chimalavera Regional Natural Park: photo WR Branch) .
Figure 3 from: Branch WR, Haacke W, Vaz Pinto P, Conradie W, Baptista N, Verburgt L, Verisimmo L (2017) Loveridge's Angolan geckos, Afroedura karroica bogerti and Pachydactylus scutatus angolensis (Sauria, Gekkonidae): new distribution records, comments on type localities and taxonomic status. Zoosystematics and Evolution 93(1): 157-166. https://doi.org/10.3897/zse.93.10915
Figure 3 - Geographical distribution of Afroedura bogerti. Insert (left) shows the polygon that encompasses the area from which the type specimen was collected. The problematic Namibian specimen is included.
Figure 4 from: Branch WR, Haacke W, Vaz Pinto P, Conradie W, Baptista N, Verburgt L, Verisimmo L (2017) Loveridge's Angolan geckos, Afroedura karroica bogerti and Pachydactylus scutatus angolensis (Sauria, Gekkonidae): new distribution records, comments on type localities and taxonomic status. Zoosystematics and Evolution 93(1): 157-166. https://doi.org/10.3897/zse.93.10915
Figure 4 - Regional variation in colouration and habitus of Afroedura bogerti from Angola A Omauha Lodge, Namibe Province B 52 km N Caraculo, Namibe Province C Praia do Meva, Benguela Province (P Vaz Pinto). D Candumbo Rocks, Huambo Province (L Verburgt). All photos by WR Branch, except where noted.
Figure 5 from: Branch WR, Haacke W, Vaz Pinto P, Conradie W, Baptista N, Verburgt L, Verisimmo L (2017) Loveridge's Angolan geckos, Afroedura karroica bogerti and Pachydactylus scutatus angolensis (Sauria, Gekkonidae): new distribution records, comments on type localities and taxonomic status. Zoosystematics and Evolution 93(1): 157-166. https://doi.org/10.3897/zse.93.10915
Figure 5 - Distribution of Pachydactylus angolensis and Pachydactylus scutatus in Angola. Stars = type localities. For additional Namibian localities for Pachydactylus scutatus, see Bauer et al. (2002).
Figure 2 from: Branch WR, Haacke W, Vaz Pinto P, Conradie W, Baptista N, Verburgt L, Verisimmo L (2017) Loveridge's Angolan geckos, Afroedura karroica bogerti and Pachydactylus scutatus angolensis (Sauria, Gekkonidae): new distribution records, comments on type localities and taxonomic status. Zoosystematics and Evolution 93(1): 157-166. https://doi.org/10.3897/zse.93.10915
Figure 2 - The ruins of farm Monte Verde, surrounded by eucalyptus trees (middle distance), overlay those of William Chapman's farm Monte Victoria-Verdun. Viewed from an intrusive rock outcrop on the lower northern slopes of Sandula Hill.
Figure 1 from: Branch WR, Haacke W, Vaz Pinto P, Conradie W, Baptista N, Verburgt L, Verisimmo L (2017) Loveridge's Angolan geckos, Afroedura karroica bogerti and Pachydactylus scutatus angolensis (Sauria, Gekkonidae): new distribution records, comments on type localities and taxonomic status. Zoosystematics and Evolution 93(1): 157-166. https://doi.org/10.3897/zse.93.10915
Figure 1 - A: (left) Photograph of the original "Titulo de Concessao" (28 January 1930) confirming William Chapman's ownership of the farm that was purchased by the Kath-Brock family. B: (right) the farm map from the "Titulo de Concessao" showing 'Alengo Sandula' at middle of lower boundary.
Рис. 3. Точки нахоΔок Orthosia ariuna: 1 — МонгоΛия, аймак БуΛган, 64 км З ЭрΔэнэсанта (типовая местность); 2 — Россия, РеспубΛика Тыва, Эрзин; 3 — Россия, ЗабайкаΛьский край, Нижний Цасучей; 4 — Россия, Хабаровск (новая нахоΔка);? — Россия, Приморский край, Уссурийск (сомнитеΛьное указание) Fig. 3. Distribution records of Orthosia ariuna: 1 — Mongolia, Bulgan aimak, 64 km W of Erdenesant (type locality); 2 — Russia, Republic of Tyva, Erzin; 3 — Russia, Zabaykalsky Krai, Nizhny Tsasuchey; 4 — Russia, Khabarovsk (new record);? — Russia, Primorsky Krai, Ussuriisk (questionable record) in The First Reliable Record Of A Little-Known Species Orthosia Ariuna Hreblay, 1991 (Lepidoptera, Noctuidae) From The Far East Of Russia
Рис. 3. Точки нахоΔок Orthosia ariuna: 1 — МонгоΛия, аймак БуΛган, 64 км З ЭрΔэнэсанта (типовая местность); 2 — Россия, РеспубΛика Тыва, Эрзин; 3 — Россия, ЗабайкаΛьский край, Нижний Цасучей; 4 — Россия, Хабаровск (новая нахоΔка);? — Россия, Приморский край, Уссурийск (сомнитеΛьное указание) Fig. 3. Distribution records of Orthosia ariuna: 1 — Mongolia, Bulgan aimak, 64 km W of Erdenesant (type locality); 2 — Russia, Republic of Tyva, Erzin; 3 — Russia, Zabaykalsky Krai, Nizhny Tsasuchey; 4 — Russia, Khabarovsk (new record);? — Russia, Primorsky Krai, Ussuriisk (questionable record)
Fig. 1. The map showing the localities where the examined materials were collected from 1981 in A new species and new record of Pacificincolidae (Bryozoa: Cheilostomata) from Korea
Fig. 1. The map showing the localities where the examined materials were collected from 1981 to 2020. 1, Geojin Port (Goseong-gun); 2, Jodo Island (Yangyang-gun); 3, Namae Port (Yangyang-gun); 4, Jumunjin Port (Gangneung-si); 5, Gyeongpodae (Gangneung-si); 6, Neunggeol (Ulleungdo Island); 7, Deoksan Port (Samcheok-si); 8, Ganggu Port (Yeongdeok-gun); 9, Guryongpo Port (Pohang-si); 10, Yangpo Port (Pohang-si); 11, Gampo Port (Gyeongju-si); 12, Bangeojin Port (Ulsan); 13, Jangsaengpo Port (Ulsan); 14, Daebyeon Port (Busan); 15, Mipo Port (Busan); 16, Suyabangdo Island (Geoje-si); 17, Gujora Port (Geoje-si); 18, Daetseom Island (Geoje-si); 19, Daegueulbido Island (Tongyeong-si); 20, Hongdo Island (Tongyeong-si); 21, Tongyeong Consignment Market (Tongyeong-si); 22, Sindo Island (Tongyeong-si); 23, Yokjido Island (Tongyeong-si); 24, Sangju-ri (Namhae-gun); 25, Gwangyang Port (Gwangyang-si); 26, Almado Island (Yeosu-si); 27, Gyedo Island (Goheung-gun); 28, Jeju Port (Jeju-do); 29, Seogwipo Port (Jeju-do); 30, Munseom Island (Jeju-do); 31, Gangjeong (Jeju-do); 32, Gapado Island (Jeju-do); 33, Hauido Island (Sinan-gun); 34, Hoenggyeongdo Island (Gunsan-si); 35, Cheongpodae Beach (Taean-gun); 36, Sinjindo (Taean-gun); 37, Hagampo Beach (Taean-gun); 38, Incheon Port (Incheon); 39, Baengnyeongdo Island (Incheon). ●, Pacificincola perforata; ■, Primavelans glabricollaris n. sp.; ★, Pacificincola perforata + Primavelans glabricollaris n. sp.
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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.