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Linked collectors and determiners for: A revision of the Myopsalta crucifera (Ashton) species group (Hemiptera: Cicadidae: Cicadettini) with 14 new species from mainland Australia.
Natural history specimen data linked to collectors and determiners held within, "A revision of the Myopsalta crucifera (Ashton) species group (Hemiptera: Cicadidae: Cicadettini) with 14 new species from mainland Australia". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/3f7df4de-b7dc-4376-b808-e479925a5ee4">https://bionomia.net/dataset/3f7df4de-b7dc-4376-b808-e479925a5ee4</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/3f7df4de-b7dc-4376-b808-e479925a5ee4">https://gbif.org/dataset/3f7df4de-b7dc-4376-b808-e479925a5ee4</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: Revision of Chassalia (Rubiaceae-Rubioideae-Palicoureeae) in Borneo, with 14 new species.
Natural history specimen data linked to collectors and determiners held within, "Revision of Chassalia (Rubiaceae-Rubioideae-Palicoureeae) in Borneo, with 14 new species". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/02cf5931-b18e-4d58-a6ff-9c7b1e37e68d">https://bionomia.net/dataset/02cf5931-b18e-4d58-a6ff-9c7b1e37e68d</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/02cf5931-b18e-4d58-a6ff-9c7b1e37e68d">https://gbif.org/dataset/02cf5931-b18e-4d58-a6ff-9c7b1e37e68d</a>. Formatted as a Frictionless Data package.
FIG. 14 in New Cenozoic Muricidae (Mollusca: Gastropoda) from Europe
FIG. 14. — Spiral cords and internal denticles of the outer lip in Timbellus crenulatus tricarinatus (Lamarck, 1803) (A-C) and T. curvispina n. sp. (D-H): A, original figure of Lamarck (1816: pl. 418, fig. 5a), Thiverval-Grignon, Yvelines, Paris Basin, France, middle Eocene (Lutetian); B, C, neotype designated herein, MNHN.F.A90547 (MNHN coll.), Thiverval-Grignon (Falunière); D, paratype, MNHN.F.A73848 (Pons coll.), Fontenay-en-Vexin (Bois-du-But), Eure, Paris Basin, France, middle Eocene (Lutetian); E, F, holotype, MNHN.F.A90541 (MNHN coll.), Parnes, Oise, middle Eocene (Lutetian); G, H, paratype, MNHN.F.A90543 (Pons coll.), Fontenay-en-Vexin. Scale bars: B-H, 10 mm. Credits: P. Loubry.
Fig. 14 in Stick insects from Vietnam: The new genus Mycovartes gen. nov., with two new species and two new species of Neooxyartes Ho, 2018 (Phasmida: Lonchodidae: Necrosciinae)
Fig. 14. Mycovartes montanus gen. et sp. nov., eggs (RBINS). A. Lateral view. B. Dorsal view. C. Operculum. D. Ventral view. E. Dorsolateral view. F. Anterolateral view. G. Posterodorsal view. H. Polar area. I. Variation.
Fig. 14. a–c. Iris senegalensis Beier, 1931 in An annotated type catalogue of praying mantises (Mantodea) in the Zoological Museum Hamburg (ZMH)
Fig. 14. a–c. Iris senegalensis Beier, 1931, holotype, ♂ (ZMH 841110). a. Labels. b. Dorsal view. c. Ventral view. d–g. Oxyelaea heteromorpha Beier, 1930, paratype, ♀ (ZMH 833031). d. Labels. e. Dorsal view. f. Ventral view. g. Lateral view. Scale bars = 10 mm.
Fig. 14 in On new genera and species of crack-leg spiders (Araneae, Udubidae) from Madagascar
Fig. 14. Zorascar pasunepipe gen. et sp. nov., holotype male (BE_RMCA_ARA.Ara.247343; RMCA). A. Male right palp (mirrored), retrolateral view. B. Idem, ventral view. C. Idem, dorsal view. D. Idem, bulbus, retrolateral view. E. Idem, ventral view. F. Idem, prolateral view. Abbreviations: C = conductor; CE = cymbial retrobasal extension; E = embolus; MA = median apophysis; Pc = paraconductor; RTA = retrolateral tibial apophysis; SL = subtegular locking lobe; TL = tegular locking lobe. Scale bars: A–C = 0.5mm; D–F = 0.2 mm. Stacked microphotographs by Arnaud Henrard and Rudy Jocqué.
Figure 14. A, B in giant, spike-toothed salmon, Oncorhynchus rastrosus and the "Proto-Tuolumne River" (early Pliocene) of Central California
Figure 14. A, B. Measurements of O. rastrosus premaxillary teeth (31 specimens total), freshwater (pink/red) vs. coastal marine (grey/black). A. Average lengths of osseous bases. B. Average lengths of tooth cusps. Freshwater specimens are from the Mehrten Formation (pink) and Pinole Formation (red). Coastal marine specimens are from the Monterey, Santa Margarita, and Capistrano formations. How measurements were taken is shown in Fig. 10).
FIG. 14 in Horses in the suburbs of a medieval city - a case study from Brno (Czech Republic)
FIG. 14. — Robusticity Comparison of the ratio of measurements SD/GL*100 on horse metacarpals (left) and metatarsals (right) from Brno with the mean ratios of horses from Czech Medieval sites and modern specimens of Arabian horse, heavy horse, and Equus caballus przewalskii Poliakov, 1881. Abbreviations:GL, greatest length; SD, smallest width of the diaphysis.
Monthly precipitation intensity maxima for 14 aggregation times at 132 stations in Germany
<p>This dataset contains monthly precipitation intensity maxima for 14 aggregation times at 132 stations in Germany that serve as the basis of the study<em> Modeling seasonal variations of extreme rainfall on different time scales in Germany.</em></p> <p> </p> <p><strong>Generation of the dataset:</strong><br> We use precipitation measurements at 132 stations in Germany that provide a temporal resolution of one minute. The majority (129) of these stations are operated by the German Meteorological Service (DWD) and were obtained via ftp://ftp-cdc.dwd.de/climate_environment/CDC/observations_germany/climate. The available time series at these stations range from 19 to 28 years. Additionally we use three stations operated by the Wupperverband (https://www.wupperverband.de) with time series of more than 43 years.</p> <p>The observations were accumulated to the following durations: <span class="math-tex">\(d \in 2^{\left\lbrace 0,1,2,..,13 \right\rbrace}\,\text{min} = \left\lbrace 1,2,4,...,8192 \right\rbrace\,\text{min}\)</span>. Thus, resulting in 14 time series per station.</p> <p> </p> <p><strong>Files and variables</strong></p> <p>meta_data_seasonal_variations_IDF_germany.csv</p> <ul> <li>Meta information about the stations</li> <li>Variables: station name, station id (as provided by DWD), position (longitude, latitude), length of timeseries available</li> <li>Variable names: "StationName", "StationID", "Longitude", "Latitude", "NumberYears"</li> </ul> <p>monthly_maxima_seasonal_variations_IDF_germany.csv</p> <ul> <li>Monthly maxima for different durations (aggregation times)</li> <li>Variables: station id (as in meta file), year and month of observation, duration [h], observed monthly intensity maximum [mm/h]</li> <li>Variable names: "StationID", "Year", "Month", "Duration [h]", "MonthlyIntensityMaximum [mm/h]"</li> </ul> <p> </p> <p><strong>Abstract of the study</strong></p> <p>We model monthly precipitation maxima at 132 stations in Germany for a wide range of durations from one minute to about six days using a duration-dependent generalized extreme value (d-GEV) distribution with monthly varying parameters. This allows for the estimation of both monthly and annual intensity--duration--frequency (IDF) curves:<br> (1) The monthly IDF curves are steeper in summer and exhibit higher intensities for short durations than in the rest of the year. Thus, everywhere in Germany short convective extreme events occur very likely in summer. In contrast, extreme events with a duration of several hours up to about one day are more likely to occur within a longer period or even spread throughout the whole year, depending on the station. There are major differences within Germany with respect to the months in which long-lasting stratiform extreme events are more likely to occur. At some stations the IDF curves (for a given quantile) for different months intersect. The meteorological interpretation of this intersection is that the season at which a certain extreme event is most likely to occur shifts from summer towards autumn or winter for longer durations.<br> (2) We compare the annual IDF curves resulting from the monthly model with those estimated conventionally, that is, based on modeling annual maxima. We find that adding information in the form of smooth variations during the year leads to a considerable reduction of uncertainties. We additionally observe that at some stations, the annual IDF curves obtained by modeling monthly maxima deviate from the assumption of scale invariance, resulting in a flattening in the slope of the IDF curves for long durations.</p> <p> </p> <p><strong>Acknowledgements</strong></p> <p>The authors would like to thank the Wupperverband, and in particular Marc Scheibel, as well as the Climate Data Center of the DWD, for providing and maintaining the precipitation time series.</p>
Fig. 14 in Quaternary time scales for the Pontocaspian domain: Interbasinal connectivity and faunal evolution
Fig. 14. The successive mollusc faunas in the Pontocaspian region provide clear insights into basin connection and isolation. Age and MIS zonation from Cohen et al. (2013). H = Holocene; LP = Late Pleistocene. Regional phases: CN = Chernomorian; Ne = Neoeuxinian; Ka = Karangatian; Uz = Uzunlarian; Ch= Chaudian; Gu = Gurian; Ku = Kujalnikian; NC = Novocaspian; Kv = Khvalynian; Hi = Hircanian; u-Kz = upper or late Khazarian; l-Kz = lower or early Khazarian; Ba = Bakunian; Ap = Apsheronian; Ak = Akshagylian. Representative bivalve species: (1) Flexopecten glaber; (2) Didacna pseudocrassa; (3) Didacnocatilus guriensis; (4) Submonodacna pleistopleura; (5) Avicardium rariiferum; (6) Avimactra subcaspia; (7) Apsheronia raricostata s.l.; (8) Apsheronia propinqua s.l.; (9) Didacna subpyramidata (1) from Büyükmeriç et al., 2016; (2) from Nevesskaya, 2007; (5-8) from Kolesnikov, 1940.
Fig. 14 in Taxonomy of Micronectidae (Heteroptera: Nepomorpha) from Vietnam, with descriptions of 11 new species
Fig. 14. Morphological features of species of Micronecta Kirkaldy, 1897, ♂♂. A–D. M. ornitheia Nieser, Chen & Yang, 2005 (ZVNU). E–G. M. tuwanoni Nieser, Chen, Leksawasdi, Thanyakam & Duangsupa, 2004 (ZVNU). A = median lobe of sternite VII; B, E = free lobe; C, F = right paramere; D, G = left paramere.
Fig. 14. Plesiastropecten hallovensis Peyer, 1944. A in The fossil record of the family Benthopectinidae (Echinodermata, Asteroidea), a reappraisal
Fig. 14. Plesiastropecten hallovensis Peyer, 1944. A. Holotype (MZA L13a), the original of Peyer (1944: pl. 7) and Blake (1984: fig. 1a–h). B. Enlargement of distal arm. C–F. Line drawings of MZA L 13b/32a–e. C. Ossicle distribution of entire individual; note large, stellate abactinal ossicles which each carry a large boss for attachment of a single spine. D. Ambulacral ossicle, in abactinal view, and two abactinal ossicles. E. Adambulacral ossicle with spines attached. F. Two marginal ossicles, with serrated spines attached. Provenance: Lower Jurassic (Hettangian, liasicus ammonite Zone) of Hallau, Canton Schaffhausen, Switzerland. Scale bars: A = 10 mm; B–C = 5 mm; D–G = 2 mm.
Fig. 14 in Revision of the genus Exosehirus (Heteroptera: Cydnidae), with the description of two new species
Fig. 14. Female terminalia of Exosehirus elamensis sp. nov. A – terminalia in dorsal view (female with folded gynatrial cone); B – straight gynatrial cone of another female, in dorsoposterior view. Scale bar: 0.25 mm.
Fig. 14 in Revision of the intertidal rove beetle genus Bryothinusa from Japan (Coleoptera: Staphylinidae: Aleocharinae)
Fig. 14. Bryothinusa aikoae sp. nov. A – labrum; B – mandible, dorsal view; C – lacinia, dorsal view; D – labium; E – mentum; F – female sternite VIII; G – spermatheca. Scale bars: 0.1 mm.
Fig. 14 in Review of the genus Cavelerius (Heteroptera: Blissidae) with descriptions of three new species from China and Southeast Asia
Fig. 14. Cavelerius nigrivena sp. nov. a – female abdominal dorsum, dorsal view; b – basal part of female abdominal dorsum, enlarged; c – pygophore, posterodorsal view; d–g – left paramere, four different aspects; h–j – phallus, three different aspects; k – sperm reservoir and adjoining portion of phallus, dorsal view.
Fig. 14 in The family Epimetopidae (Coleoptera: Hydrophiloidea): review of current knowledge, genus-level phylogeny, and taxonomic revision of Eupotemus
Fig. 14. Habitus photographs of the known species of Eumetopus Balfour-Browne, 1949. A – E. acutimontis Ji & Jäch, 1998, paratype from China: Hainan (NHMW); B – E. asperatus (Champion, 1919), specimen from Nepal: Koshi Valley (NMPC); C – E. bullatus (Sharp, 1875), specimen from India: Maharashtra, Sawantwadi (NMPC); D – E. flavidulus (Sharp, 1890), specimen from India: Meghalaya, Bagmara (NHMW); E – E. maindroni (Régimbart, 1903), specimen from India: Maharashtra, Sawantwadi (NHMW); F – E. schuelkei Jäch, 2002, paratype from central Laos; G – E. tibialis Ji & Jäch, 1998 from Thailand, Ban Na env. (NMPC); H – E. weigeli Skale & Jäch, 2003, holotype from Nepal (NHMW). Scale bars: 1 mm.
Figures 14–26 in Synopsis of the tribe Platynini in New Zealand (Coleoptera: Carabidae)
Figures 14–26. Mentum: 14) medial tooth bifid; 15) emarginate; 16) subtruncate; 17) subtriangular; 18) acute; 19) circular foveae large; 20) small; 21) with numerous short setae; 22) without short setae. Metacoxae: 23) with 3–4 posteroventral setae; 24) with 2 setae. Cleaning organ of protibia: 25) with 2 clip setae; 26) with 3 clip setae.
Figures 13–14. Xestipyge skelleyi, male. 13 in A brief review of the New World Xestipyge Marseul (Coleoptera: Histeridae: Dendrophilinae: Paromalini) with description of a new species from the southwestern USA
Figures 13–14. Xestipyge skelleyi, male. 13) Pygidia and elytral apices, apicodorsal view. 14) Lateral habitus.
Figuras 14–16 in Especies nuevas de Lasioglossum Curtis de las altas montañas de las Antillas Mayores y estado actual del conocimiento del taxon Habralictellus Moure y Hurd (Hymenoptera: Apoidea: Halictidae)
Figuras 14–16. Lasioglossum darlingtoni sp. nov. Terminalia del macho. 14) Genitales en vista ventral. 15) Genitales en vista dorsal. 16) Esternos 7 y 8 fusionados. Escala = 0,3 mm.
Figures 12–17. Phyllophaga benwarneri tarsal claws, lateral view. 12, 13, 14 in Two new scarab beetles from the southwestern USA (Coleoptera: Scarabaeidae: Melolonthinae and Aphodiinae)
Figures 12–17. Phyllophaga benwarneri tarsal claws, lateral view. 12, 13, 14) Male pro-, meso- and metatarsi, respectively. 15, 16, 17) Female pro-, meso- and metatarsi, respectively.
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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.