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3,101 results for “Historical”
FIGURE 1 in A historical review of praying mantid taxonomy and systematics in the Neotropical Region: State of knowledge and recent advances (Insecta: Mantodea)
FIGURE 1. Historical trend of mantid species descriptions, 1758–2010 (valid species only). Sudden increase in the number of species described by year 1869 corresponds to the beginning of activities of H. de Saussure on mantid taxonomy. Steady increase to 1939 was due to activities of J.O. Westwood, E. Giglio-Tos, L. Chopard, J.A.G. Rehn, M. Hebard and M. Beier (63% of all known Neotropical mantid species were described between 1869 and 1939). Interest plateaued until early 1980's when Neotropical mantid taxonomy experienced renewed interest.
FIGURE 6 in Type specimens in the Port Elizabeth Museum, South Africa, including the historically important Albany Museum collection. Part 1: Amphibians
FIGURE 6. Family Heleophrynidae and Hyperoliidae: A—Holotype of Heleophryne hewitti (PEM A11156), B—Lectotype of Heleophryne rosei (PEM A1541), C—Holotype of Kassina wealii quinque-vittata (PEM A6289).
FIGURE 2 in Type specimens in the Port Elizabeth Museum, South Africa, including the historically important Albany Museum collection. Part 1: Amphibians
FIGURE 2. Family Breviciptidae: A—Holotype of Breviceps acutirostris (PEM A1540), B—Lectotype of Breviceps fuscus (PEM A4826), C—Lectotype of Breviceps tympanifer (PEM A4811), D—Lectotype of Breviceps parvus (PEM A1534), E—Lectotype of Breviceps parvus caffer (PEM A849).
FIGURE 1. Family Pyxicephalidae I in Type specimens in the Port Elizabeth Museum, South Africa, including the historically important Albany Museum collection. Part 1: Amphibians
FIGURE 1. Family Pyxicephalidae I: A—Lectotype of Anhydrophryne rattrayi (PEM A6334), B—Lectotype of Arthroleptella bicolor villiersi (PEM A1568), C—Holotype of Arthroleptella drewesii (PEM A2319), D—Holotype of Arthroleptella landdrosia (PEM A7123).
FIGURE 5. Family Pyxicephalidae II in Type specimens in the Port Elizabeth Museum, South Africa, including the historically important Albany Museum collection. Part 1: Amphibians
FIGURE 5. Family Pyxicephalidae II: A—Holotype of Cacosternum thorini (PEM A10091), B—Holotype of Cacosternum karooicum (PEM A5459), C—Holotype of Poyntonia paludicola (PEM A1600), D—Lectotype of Natalobatrachus bonebergi (PEM A1549), E—Lectotype of Cacosternum capense (PEM A4963).
FIGURE 8 in Type specimens in the Port Elizabeth Museum, South Africa, including the historically important Albany Museum collection. Part 1: Amphibians
FIGURE 8. Family Pyxicephalidae III: A—Lectotype of Rana vertebralis (PEM A1550), B—Holotype of Strongylopus springbokensis (PEM A963), C—Holotype of Tomopterna tandyi (PEM A2283).
FIGURE 7 in Type specimens in the Port Elizabeth Museum, South Africa, including the historically important Albany Museum collection. Part 1: Amphibians
FIGURE 7. Family Hyperoliidae: A—Holotype of Hyperolius chelaensis (PEM A9223), B—Lectotype of Hyperolius horstockii semidiscus (PEM A4579), C—Holotype of Hyperolius raymondi (PEM A10049).
FIGURE 4. Family Bufonidae II in Type specimens in the Port Elizabeth Museum, South Africa, including the historically important Albany Museum collection. Part 1: Amphibians
FIGURE 4. Family Bufonidae II: A—Lectotype of Bufo regularis pardalis (PEM A837), B—Lectotype of Bufo regularis rangeri (PEM A822).
FIGURE 3. Family Bufonidae I in Type specimens in the Port Elizabeth Museum, South Africa, including the historically important Albany Museum collection. Part 1: Amphibians
FIGURE 3. Family Bufonidae I: A— Lectotype of Bufo fenoulheti rhodesianus (PEM A9079), B—Lectotye of Bufo fenoulheti (PEM A825), C— Lectotype of Bufo angusticeps amatolica (PEM A828), D—Holotype of Bufo robinsoni (PEM A2492), E— Holotype of Bufo gariepensis nubicola (PEM A2513), F—Lectotype of Bufo rosei (PEM A5132).
FIGURES 4–11 in A new species of Lilophaea Bechyné (Coleoptera, Chrysomelidae, Galerucinae) with a historical background and a checklist of the genus
FIGURES 4–11. Lilophaea sulina sp. nov., paratype male: 4, ventrite V and genitalia; 5, ventrite V; aedeagus: 6, ventral view, 7, lateral view; paratype female: 8, ventrite V and genitalia; 9, sternite VIII; 10, vaginal palpi; 11, spermatheca (ap, apodeme; bc, bursa copulatrix; e, spermatheca; i, intestine; o, basal orifice; sc, sclerite of the internal sac; sg, spiculum gastrale; t, tegmen). Scale bars: figs 1–9 = 0.25 mm; figs 10, 11 = 0.1 mm.
FIGURES 1–3 in A new species of Lilophaea Bechyné (Coleoptera, Chrysomelidae, Galerucinae) with a historical background and a checklist of the genus
FIGURES 1–3. Lilophaea sulina sp. nov., holotype male: 1, habitus, dorsal view. Length = 3.9 mm. 2, head, frontal view; 3, habitus, lateral view.
FIGURE 1 in Catalogue and Bibliography of the Hong Kong Carabidae Latreille, 1802 (Coleoptera: Adephaga), with notes on the historic boundaries of Hong Kong as related to zoological collections
FIGURE 1. Map of the Hong Kong Special Administartive region of China in 2016. Note the coastline is significantly different from that of 1841, due to reclamation.
FIGURE 1 in Historical considerations and comments on the type series of Cyrtodactylus marmoratus Gray, 1831, with an updated comparative table for the bent-toed geckos of the Sunda Islands and Sulawesi
FIGURE 1. Precloacal region of Cyrtodactylus marmoratus. (A) Lectotype of C. marmoratus (RMNH.RENA. 2710a.1; adult male) with a precloacal groove as typical for males of that species. (B) Paralectotype of C. marmoratus (RMNH.RENA. 2710.3; adult female) lacking a precloacal depression as typical for females of that species. Photographs are not to scale. Plate prepared by Max Kieckbusch based on photographs by Sven Mecke.
FIGURE 2 in Historical considerations and comments on the type series of Cyrtodactylus marmoratus Gray, 1831, with an updated comparative table for the bent-toed geckos of the Sunda Islands and Sulawesi
FIGURE 2. Precloacal regions of six Sundanese and Sulawesi species of Cyrtodactylus showing differences in the expression of a precloacal depression in adult males. (A) C. pubisulcus (AMNH R111889) possessing a slit-like precloacal groove, with the pore-bearing scales sunk deeply into the depression and not visible. (B) C. klakahensis (SMF 22476; holotype) possessing a slit-like precloacal groove, with the pore-bearing scales sunk deeply into the depression and barely visible. (C) C. fumosus (BMNH 1896.12.9.3) possessing a precloacal groove, with the enlarged pore-bearing scales arranged in the shape of an inverse 'Y' with the groove broadening posteriorly. (D) C. baluensis (MCZ.Herp R-39036) possessing a precloacal pit, with the porebearing scales from the left and right side of the posterior-most precloacal scale series arranged in the shape of an inverse 'V' and widely separated from each other, creating a depression in the form of an acute triangle. (E) C. consobrinus (MCZ.Herp R- 102031) possessing a precloacal pit in the form of an obtuse triangle. (F) C. wetariensis (AMNH R32165; holotype) lacking a precloacal depression. Photographs are not to scale. Plate prepared by Max Kieckbusch based on photographs by Sven Mecke.
Historical changes in drought characteristics and its impact on vegetation cover over Madagascar
<p>The uploaded data represent the results of our research about "Historical changes in drought characteristics and its impact on vegetation cover over Madagascar".</p>
Calgary Historical Property Assessements, 2019 (Residential Properties)
Open the record for dataset details and reuse information.
Fig. 8 in Historical and Contemporary Occurrence ofCylindera(s. str.)celeripes(LeConte) (Coleoptera: Carabidae: Cicindelinae) and Implications for Its Conservation
Fig. 8. Historical and currently known geographical occurrence of Cylindera celeripes by county. Red = last record prior to 1920; orange = last record 1941–1960 ("?" = questionable record); green = last record 1991–1996; blue = last record 2005–2011.
Figs. 2–7 in Historical and Contemporary Occurrence ofCylindera(s. str.)celeripes(LeConte) (Coleoptera: Carabidae: Cicindelinae) and Implications for Its Conservation
Figs. 2–7. Habitats of Cylindera celeripes. 2) Western Iowa (Pottawattamie Co., Hitchcock Nature Center, Badger Trail); adults were active in moderately vegetated 2-track below road cut; 3) Northwestern Oklahoma (Woodward Co., Alabaster Caverns State Park, upper Nature Trail); adults were active amongst sparse vegetation in lichen-encrusted clay/gypsum exposures; 4) Northwestern Oklahoma (Major Co., Glass Mountains State Park); adults were active amongst sparse vegetation in lichen-encrusted clay/gypsum exposures on top of butte; 5) Northwestern Oklahoma (Major Co., Glass Mountains, vic. Scenic Overlook); adults were active in sparsely vegetated clay exposures in undisturbed areas of lower talus slopes and on top of neighboring butte; 6) Northwestern Missouri (Atchison Co., Star School Hill Prairie Natural Area, south tract); adults were seen amongst rather dense vegetated on upper slopes along the center foreground path; 7) Northwestern Missouri (Atchison Co., Brickyard Hill Conservation Area, High Creek Prairie); adults were active in sparsely vegetated clay exposures on and below lower slopes.
Fig. 1 in Historical and Contemporary Occurrence ofCylindera(s. str.)celeripes(LeConte) (Coleoptera: Carabidae: Cicindelinae) and Implications for Its Conservation
Fig. 1. Cylindera celeripes adults at: a) Hitchcock Nature Center, Pottawattamie Co., IA (13 July 2008); b) Alabaster Caverns State Park, Woodward Co., OK (10 June 2009); c) Same locality as "b", note parasite (possibly Hymenoptera: Dryinidae) protruding from abdomen and ant head attached to right antenna; d) Brickyard Hill Natural Area, Atchison Co., MO (27 June 2009).
Fig. 5 in Across mountains and ocean: species delimitation and historical connectivity in Holarctic and Arctic-Alpine wolf spiders (Lycosidae, Pardosa)
Fig. 5. Introgression in P. saltuaria species group, n = 84, m = 43 datasets. P.hyper.FIN—Finnish P. hyperborea, P.hyper.GR—Greenland P. hyperborea; (a, c, e) de novo assembly; (b, d, f) reference assembly. (a, b) Fbranch D-statistics summary: dotted lines indicate internal node branches, fb—f-branch estimates of admixture; (c, d) fastsimcoal2 scenarios with the highest support: Ne effective population size of corresponding species/population (see fastsimcoal2 section in Supplementary Material for details about codes in brackets); tm—time of population/species merge (split) in generations; tadm—time of admixture in generations; adm—admixture fraction; (e, f) PhyloNetworks: colored lines and numbers indicate direction and proportion of admixture.
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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.