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FIGURES 21a–e. Halictus pulvereus Morawitz, 1874 in The type specimens of bees (Hymenoptera, Apoidea) deposited in the Zoological Institute of the Russian Academy of Sciences, St. Petersburg. Contribution III Family Halictidae, genera Halictus Latreille, 1804, and Sphecodes Latreille, 1804
FIGURES 21a–e. Halictus pulvereus Morawitz, 1874. Lectotype, female: a—habitus, lateral view; b—metasoma, dorsal view; c—mesosoma, dorsal view; d—head, frontal view; e—labels.
FIGURES 39a–e in The type specimens of bees (Hymenoptera, Apoidea) deposited in the Zoological Institute of the Russian Academy of Sciences, St. Petersburg. Contribution III Family Halictidae, genera Halictus Latreille, 1804, and Sphecodes Latreille, 1804
FIGURES 39a–e. Sphecodes turanicus Astafurova & Proshchalykin, 2017. Holotype, female: a—habitus, lateral view; b—mesosoma, dorsal view; c—head, frontal view; d—metasoma, dorsal view; e—labels.
FIGURES 37a–f in The type specimens of bees (Hymenoptera, Apoidea) deposited in the Zoological Institute of the Russian Academy of Sciences, St. Petersburg. Contribution III Family Halictidae, genera Halictus Latreille, 1804, and Sphecodes Latreille, 1804
FIGURES 37a–f. Sphecodes pesenkoi Astafurova & Proshchalykin, 2018. Holotype, male: a—habitus, lateral view; b—metasoma, dorsal view; c—head, frontal view; d—mesosoma, dorsal view; e—labels; f—genitalia, dorsal view.
FIGURES 25a–e in The type specimens of bees (Hymenoptera, Apoidea) deposited in the Zoological Institute of the Russian Academy of Sciences, St. Petersburg. Contribution III Family Halictidae, genera Halictus Latreille, 1804, and Sphecodes Latreille, 1804
FIGURES 25a–e. Halictus tataricus Blüthgen, 1933. Lectotype, female: a—habitus, lateral view; b—metasoma, dorsal view; c—mesosoma, dorsal view; d—head, frontal view; e—labels.
FIGURES 33a–e. Sphecodes gracilior Morawitz, 1893 in The type specimens of bees (Hymenoptera, Apoidea) deposited in the Zoological Institute of the Russian Academy of Sciences, St. Petersburg. Contribution III Family Halictidae, genera Halictus Latreille, 1804, and Sphecodes Latreille, 1804
FIGURES 33a–e. Sphecodes gracilior Morawitz, 1893. Lectotype, male: a—habitus, lateral view; b—metasoma, dorsal view; c—mesosoma, dorsal view; d—head, frontal view; e—labels.
FIGURES 36a–f in The type specimens of bees (Hymenoptera, Apoidea) deposited in the Zoological Institute of the Russian Academy of Sciences, St. Petersburg. Contribution III Family Halictidae, genera Halictus Latreille, 1804, and Sphecodes Latreille, 1804
FIGURES 36a–f. Sphecodes orientalis Astafurova & Proshchalykin, 2014. Holotype, male: a—habitus, lateral view; b—metasoma, dorsal view; c—mesosoma, dorsal view; d—head, frontal view; e—genitalia, dorsal view; f—labels.
FIGURES 31a–e. Seladonia leleji Pesenko, 2006 in The type specimens of bees (Hymenoptera, Apoidea) deposited in the Zoological Institute of the Russian Academy of Sciences, St. Petersburg. Contribution III Family Halictidae, genera Halictus Latreille, 1804, and Sphecodes Latreille, 1804
FIGURES 31a–e. Seladonia leleji Pesenko, 2006. Holotype, male: a—habitus, lateral view; b—head, frontal view; c—metasoma, dorsal view; d—labels; e—mesosoma, dorsal view.
FIGURES 32a–f. Seladonia nikolskayae Pesenko, 2006 in The type specimens of bees (Hymenoptera, Apoidea) deposited in the Zoological Institute of the Russian Academy of Sciences, St. Petersburg. Contribution III Family Halictidae, genera Halictus Latreille, 1804, and Sphecodes Latreille, 1804
FIGURES 32a–f. Seladonia nikolskayae Pesenko, 2006. Holotype, male: a—habitus, lateral view; b—head, frontal view; c—labels; d—metasoma, dorso-lateral view; e—mesosoma, dorsal view; f—genitalia, dorsal view.
FIGURES 1–23 in Types of Thyatirinae (Lepidoptera: Drepanidae) in the collection of the Zoological Institute of the Russian Academy of Sciences
FIGURES 1–23. Types of Thyatirinae. 1, holotype of Cymatophora albicostata Bremer, 1861 (ZISP); 2, its reproduction from Mémoires de l'Académie impériale des sciences de St.-Pétersbourg 8(1): pl. 5, fig. 6; 3, lectotype of Cymatophora octogesima var. caucasica Krulikowsky, 1901 (ZMKU: courtesy I. Kostjuk); 4, lectotype of Gonophora dieckmanni Graeser, 1888 (ZISP); 5, correct lectotype of Thyatira hedemanni Christoph, 1885 (ZISP); 6, its reproduction from the original description (pl. 2, fig. 3); 7, holotype of Thyatira derasa var. intermedia Bremer, [1864] (ZISP); 8, holotype of Tethea ocularis ssp. opa Zolotuhin, 1997 (ZISP); 9, lectotype of Thyatira moellendorfi Fixsen, 1887 (ZISP); 10—its reproduction from the original description (pl. 15, fig. 12); 11, false lectotype of Asphalia nigrofascicula Graeser, 1888 (NHML); 12, correct lectotype of A. nigrofascicula Graes. (ZISP); 13, so-called 'type' of Cymatophora tancrei Graeser, 1888, from ZMHU; 14, labels of C. tancrei enlarged and cover page of the publication issue; 15, false holotype of Cymatophora or var. terrosa Graeser, 1888 (ZMHU); 16, correct lectotype of C. or var. terrosa Graes. (ZISP); 17, lectotype of Thyatira violacea Fixsen, 1887 (ZISP); 18, its reproduction from the original description (pl. 15, fig. 11); 19, paratype of Nothoploca nigripunctata ssp. zolotarenkoi Dubatolov, 1987 (ZISP); 20, holotype of Cymatophora trifolium Alphéraky, 1895 (ZISP); 21, lectotype of Thyatira opalescens Alphéraky, 1897 (ZISP); 22, its reproduction from the original description (pl. 9, fig. 7); 23, location of Pung-Tung village on the map by Fixsen (1887).
Figure 3 in Optimizing biodiversity informatics to improve information flow, data quality, and utility for science and society
Figure 3. Examples of ways in which aggregators can make uncertainties and biases visually available to users of Primary Biodiversity Data. Such information can be employed to filter data and to quantify and correct for biases in sampling effort, respectively. (a) Georeferenced localities of a given species are simply plotted in geographic space (black dots; current practice). (b) Those same localities appear using symbologies that provide additional information; a hazy cloud indicates the radius of error for localities holding information regarding uncertainty of the georeference, and localities lacking such data appear only as hollow black circles. (c) Information appears that reflects the results of sampling effort, by showing in gray the georeferenced localities for all species belonging to a more inclusive target group (i.e., all species detected with the same techniques as the species of interest; conventions the same as in b). Note that the right-hand side of the study region lacks records for any species of the target group, suggestive of very low sampling effort there.
Figure 2 in Optimizing biodiversity informatics to improve information flow, data quality, and utility for science and society
Figure 2. Use of individual and collective Stable Unique Identifiers (e.g., DOIs) in biodiversity informatics. (a) Individual Stable Unique Identifier (I-SUI) allows linking diverse data domains for a given organism. In this example, an I-SUI links the voucher specimen and associated Primary Biodiversity Data (e.g., date and locality) of an individual mammal to information regarding various aspects of molecular- to population-level biology. (b) Collective Stable Unique Identifier (C-SUI) denotes a set (i.e., a list) of individual identifiers. For example, a C-SUI could indicate the n individual records used in a given analysis.
Figure 1 in Optimizing biodiversity informatics to improve information flow, data quality, and utility for science and society
Figure 1. Simplified overview of the interactions and flow of data among providers, aggregators, and users in biodiversity informatics. Numbers indicate the typical order of actions: 1. Aggregator receives data uploads (and periodic updates) from providers; 2. User makes a data query to aggregator's online portal; 3. Aggregator responds to query by making data available on portal (for viewing and/or download). Note that by querying a single aggregator, a user can receive data from multiple providers. Additionally, multiple intermediate aggregators typically exist, feeding into the largest ones most commonly consulted by users (e.g., GBIF).
UC Irvine's Social Science Tower
I spent too much time here ugh I miss UCI :-/ Source: Objaverse 1.0 / Sketchfab
Dataset for 'Phylogenetic Diversity vs H-Index – does genetics or culture lead conservation science?'
Open the record for dataset details and reuse information.
Data from: Revealing biases in insect observations a comparative analysis between academic and citizen science data
<p>Data and code used in the article "Revealing biases in insect observations a comparative analysis between academic and Citizen Science data".</p>
FIGURE 12. Melitturga caucasica Morawitz, 1877 in The type specimens of bees (Hymenoptera, Apoidea) deposited in the Zoological Institute of the Russian Academy of Sciences, St. Petersburg. Contribution VIII. Family Andrenidae, subfamily Panurginae
FIGURE 12. Melitturga caucasica Morawitz, 1877. Lectotype, female: a—habitus, lateral view and labels; b—head, frontal view; c—head and mesosoma, dorsal view; d—metasoma, dorsal view. Scale bar: 1 mm.
FIGURE 19. Panurginus flavipes Morawitz, 1894 in The type specimens of bees (Hymenoptera, Apoidea) deposited in the Zoological Institute of the Russian Academy of Sciences, St. Petersburg. Contribution VIII. Family Andrenidae, subfamily Panurginae
FIGURE 19. Panurginus flavipes Morawitz, 1894. Holotype, female: a—habitus, lateral view and labels; b—head, frontal view; c—labrum, dorsal view; d—head and mesosoma, dorsal view; e—metasoma, dorsal view. Scale bar: 1 mm.
FIGURE 4 in On two goby-associated snapping shrimps from the Red Sea, one of them new to science (Malacostraca: Decapoda: Alpheidae: Alpheus)
FIGURE 4. Alpheus karplusi sp. nov., shrimps in life: A, B—holotype male (cl 10.5 mm) from the Farasan Islands, Saudi Arabia (FLMNH UF 37011, left side of the carapace damaged during collection), general dorsal view (A) and detail of frontal region (B); C—paratype male (cl 11.4 mm) from the same locality (FLMNH UF 37016), major (right) cheliped, mesial view; D—male from Eilat, Israel (not deposited), dorso-frontal view of cephalothorax with chelipeds and other appendages; E, F, G—shrimps associated with Lotilia graciliosa Klausewitz, 1960, photographed in situ in Nuweiba (E), Naama Bay near Sharm-el-Sheikh (F) and Safaga (G), Egypt (not collected). Photographs by the author [A–C], Dr. Ilan Karplus [D], Sonja Ooms [E], Andrey Ryanskiy [F] and Indra Günther [G].
FIGURES 30–33 in A catalogue of the types of rove beetles (Coleoptera: Staphylinidae) deposited in the collection of Johan Heinrich Hochhuth in the National Museum of Natural History of the National Academy of Sciences of Ukraine
FIGURES 30–33. Bolitobius flavicollis (Figs 30a–30b), Xantholinus flavocinctus (Figs. 31a–31b), Oxypoda funicularis (Figs 32a–e), Gyrophaena strictula (Figs 33a–b): 30a, 31a, 32a, 33a—habitus, 32b—aedeagus, 32c–d—apical segments of aedeagus, 30b, 31b, 32e, 33b—labels. Scale bars: 1.0 mm (Figs 30a, 31a, 32a), 0.5 mm (Figs 32b–d, 33a).
FIGURE 8 in Unearthing the diversity of Japanese Magelona (Annelida: Magelonidae); three species new to science, and a redescription of Magelona japonica
FIGURE 8. Magelona japonica (NMW.Z.2022.001.0001, A–B, stained with Methyl Green; C–G, putative syntypes ZIHU 2789). A, chaetigers 6–15, dorsal view; B, chaetigers 7–15, ventral view; C, potential syntype drawn by Okuda (1937a), lateral view; D, dissected anterior fragment, dorsal view; E, prostomium and thorax, dorsal view; F, prostomium and thorax, ventral view; G, posterior fragment, lateral view. Ab = abdomen, Ach = achaetous region, BO = burrowing organ, Pg = pygidium, PH = prostomial horns, Pp = palp, Pr = prostomium, Th = thorax, numbers indicate chaetiger.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.