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Pond Area Estimates: Nine Study Regions in Alaska for 3 time periods (1950s, 1978-1982, 1999-2001) using remotely sensed images
The data are ArcGIS shapefiles by USGS quadrangle within 9 study regions: Arctic Coastal Plain, Stevens Village area, Yukon Flats, Minto Flats, Denali Flats, Talkeetna, Innoko Flats, Tetlin Flats, and Copper River Basin. Each shapefile polygon represents the shoreline of a pond as visually interpreted from each georectified remotely sensed image. All images were rectified based on at least 25 control points from 1:63 360 USGS digital raster graphics topographic maps using a second-order polynomial with a RMS error of less than one satellite image pixel (30 meters). All closed-basin ponds greater than 0.2 hectares were visually delineated and manually traced as polygons using ArcGIS. Each pond polygon has an ID and Hectares field representing the pond ID and area in hectares for the time period of the remotely sensed image.
Chlorophyll and phytoplankton composition climatological data on the Northwest Atlantic Shelf from 1978 to 2014: post-processed model data
This dataset includes 8-day composite of surface chlorophyll and bimonthly phytoplankton size composition climatological results on the Northwest Atlantic Shelf from the Gulf of Maine to the Mid-Atlantic Bight based on the physical-biological coupled model results from 1978 to 2014. Two size classes, small phytoplankton (SP) and large phytoplankton (LP), are provided. For more details please see: Zhengchen Zang, Rubao Ji, Zhixuan Feng, Changsheng Chen, Siqi Li, and Cabell S Davis (2021) Spatially varying phytoplankton seasonality on the Northwest Atlantic Shelf: a model-based assessment of patterns, drivers, and implications. ICES Journal of Marine Science, Volume 78, Issue 5, 1920-1934, https://doi.org/10.1093/icesjms/fsab102.
Figures 17–22. Bomansius gabrieli. 17–19 in A new species of Bomansius Lacroix (Coleoptera: Lucanidae) from Vanuatu, with redescriptions of its genus and its only congener, Bomansius gabrieli Lacroix, 1978
Figures 17–22. Bomansius gabrieli. 17–19) Males. 17) Dorsal habitus. 18) Ventral habitus. 19) Lateral habitus. 20–22) Females. 20) Dorsal habitus. 21) Ventral habitus. 22) Lateral habitus.
FIG. 8 in Unexpected diversity of the genus Collarina Jullien, 1886 (Bryozoa, Cheilostomatida) in the NE Atlantic-Mediterranean region: new species and reappraisal of C. balzaci (Audouin, 1826) and C. fayalensis Harmelin, 1978
FIG. 8. — Outlines of orifice, apertural bar, avicularium and portion of costate shield and gymnocyst: A, Collarina gautieri Harmelin, n. sp.; B, C. macaronensis Harmelin, n. sp.; C, C. speluncola Harmelin, n. sp. Scale bar: 100 µm (orifices), 50 µm (avicularia).
FIG. 5 in Unexpected diversity of the genus Collarina Jullien, 1886 (Bryozoa, Cheilostomatida) in the NE Atlantic-Mediterranean region: new species and reappraisal of C. balzaci (Audouin, 1826) and C. fayalensis Harmelin, 1978
FIG. 5. — Collarina fayalensis Harmelin, 1978: A-C, non-ovicelled and ovicelled autozooids showing the structure and limited extent of the costate shield, orifice dimorphism, small spines and relatively narrow avicularia; D, non-ovicelled zooid, for marginal pores; E, drawing from Harmelin (1978: fig. 9); F, distal part of a non-ovicelled zooid from a colony edge; G, proximal half of costate shield, note the distribution of pelmata and the shape of the basal intercostal spaces. Origin: Azores - Saô Miguel, Vila Franca Is., 15 m (A-C, F, G); Formigas Is., 15 m, 'Jean Charcot' Biaçores 1971, P.43 (D); Faial, 'Jean Charcot' Biaçores 1971, P.11 (E). Scale bars: A, 200 µm; B-D, 100 µm, F, 50 µm; G, 25 µm.
FIG. 3 in Unexpected diversity of the genus Collarina Jullien, 1886 (Bryozoa, Cheilostomatida) in the NE Atlantic-Mediterranean region: new species and reappraisal of C. balzaci (Audouin, 1826) and C. fayalensis Harmelin, 1978
FIG. 3. — Collarina balzaci (Audouin, 1826), NW Mediterranean: A, B, ovicelled and non-ovicelled zooids, note the abundance of large pseudopores (pelmata) on both the spinocyst and the ooecium; C, distal portion of a non-ovicelled zooid with no adventitious avicularia; D, distal portion of an ovicelled zooid, note the broader orifice, the shape of the apertural bar and the position of the adventitious avicularium; E, structure of the costate shield and the peripheral gymnocyst; F, adventitious avicularium with rostrum finely serrated, slightly hooked tip, and broad, rounded opesia; G, ancestrula with five spines, partly covered by filamentous microphyte. Origin: Marseille, Planier Islet, on Posidonia leaf. Scale bars: A, 200 µm; B, G, 100 µm; C-E, 50 µm; F, 25 µm.
FIG. 10 in Unexpected diversity of the genus Collarina Jullien, 1886 (Bryozoa, Cheilostomatida) in the NE Atlantic-Mediterranean region: new species and reappraisal of C. balzaci (Audouin, 1826) and C. fayalensis Harmelin, 1978
FIG. 10. — Collarina gautieri Harmelin, n. sp., NE Atlantic: A, Lepralia punctata Hassall, 1841: Busk 1854, pl. 96, fig. 3; B, C, ovicelled and non-ovicelled autozooids, note the typically curved spines associated with ovicells, the orientation of the avicularia and the respective extent of costate shield and gymnocyst; D, part of a young colony including the ancestrula (right) and the colony edge with 2 ovicelled zooids (left); E, non-ovicelled zooid (right) and fertile zooid with an early stage of the ooecium formation (middle), note the typical shape of the orifices and the structure of the costate shield with large marginal pelmata; F, ancestrula. Origin: B, Devon, coll. by JDB; C, NHMUK 1973.4.6.1, Raasay Sound, Scotland: Species A, Bishop (1986); D, Galicia, Malpica; E, Galicia, Ferrol; F, Algarve, coll. by JS. Scale bars: B, D, 200 µm; E, F, 100 µm.
FIG. 7 in Unexpected diversity of the genus Collarina Jullien, 1886 (Bryozoa, Cheilostomatida) in the NE Atlantic-Mediterranean region: new species and reappraisal of C. balzaci (Audouin, 1826) and C. fayalensis Harmelin, 1978
FIG. 7. — Outlines of orifice, apertural bar, avicularium and portion of costate shield and gymnocyst: A, Collarina balzaci (Audouin, 1826); B, C. fayalensis Harmelin, 1978, C, C. denticulata Harmelin, n. sp. Scale bar: 100 µm (orifices), 50 µm (avicularia).
FIG. 12 in Unexpected diversity of the genus Collarina Jullien, 1886 (Bryozoa, Cheilostomatida) in the NE Atlantic-Mediterranean region: new species and reappraisal of C. balzaci (Audouin, 1826) and C. fayalensis Harmelin, 1978
FIG. 12. — Collarina macaronensis Harmelin, n. sp.: A, B, colony edge, general view and detail with ovicelled and non-ovicelled zooids; C, oblique view: structure of costate shield, apertural bar, paired and apical avicularia; D, G, non-ovicelled zooids with typical traits: concave orifice poster, avicularia directed disto-laterally, costate shield with lower central part and digitate margin, large pelmata also present on the gymnocyst; E, Collarina balzaci (Audouin, 1826): Harmelin (1978a, fig. 8), Azores, Faial; F, distal part of non-ovicelled zooid with typical orifice, apertural bar with large and small pseudopores, and 3 spines; H, specimen from a continental area. Origin: A, B, NHMUK 1899.7.1.2105, Madeira, J.Y. Johnson leg.; C, NHMUK 1911.10.1.705, Madeira; D, F, G, MNHN-IB-2014-1927, Madeira, Baixo Is.; H, Galicia, Sisargas Is. Scale bars: A, 400 µm; B, C, 200 µm; D, H 100 µm; F, G, 50 µm.
FIG. 15 in Unexpected diversity of the genus Collarina Jullien, 1886 (Bryozoa, Cheilostomatida) in the NE Atlantic-Mediterranean region: new species and reappraisal of C. balzaci (Audouin, 1826) and C. fayalensis Harmelin, 1978
FIG. 15. — Types of ooecia in Collarina Jullien, 1886 species: A-C, kenozooidal ooecia with and without distal avicularium (A, C. speluncola Harmelin, n. sp; B, C. fayalensis Harmelin, 1978; C, C. macaronensis Harmelin, n. sp.); D, C. denticulata Harmelin, n. sp., colony portion with two kenozooidal ooecia (left) and three ooecia incorporated in distal autozooid (right); E, C. macaronensis Harmelin, n. sp., 2 ovicelled zooids with kenozooidal ooecium (left) vs ooecium incorporated in distal autozooid (right). Origin: A, Marseille, Conger Cave; B, Azores, Saô Miguel, Vila Franca Is.; C, E, Madeira, NHMUK 1911.10.1.705; D, Catalonia, Medes Is. Scale bars: A-C, E 100 µm, D, 200 µm.
Fig. 13. Hippoporina indica Pillai, 1978. – A–D in Cheilostome Bryozoa from Penang and Langkawi, Malaysia
Fig. 13. Hippoporina indica Pillai, 1978. – A–D. Kuah jetty, Langkawi, MSL BRY017b. A. Group of zooids. B. Autozooidal orifice and avicularium. C. Autozooids with closed orifices. D. Ovicell. – E. Pulau Betong, Penang, MSL BRY022; ovicell. – F. Sungai Menghulu, Langkawi, MSL BRY023; group of ovicellate zooids. Scale bars: A, C, F = 200 μm; B, D–E = 100 μm.
Fig. 1. Hemisphaerini. A–B. Macrodaruma pertinax Fennah, 1978. A. Habitus, dorsal view. B in Nomenclatural changes in the planthopper tribe Hemisphaeriini (Hemiptera: Fulgoromorpha: Issidae), with the description of a new genus and a new species
Fig. 1. Hemisphaerini. A–B. Macrodaruma pertinax Fennah, 1978. A. Habitus, dorsal view. B. Habitus, ventral view. — C–D. Neogergithoides tubercularis Sun, Meng & Wang, 2012. C. Habitus, dorsal view. D. Metope and clypeus, facial view. — E–F. Choutagus longicephalus Zhang, Wang & Che, 2006. E. Habitus, dorsal view. F. Habitus, ventral view. — G–H. Gergithoides carinatifrons Schumacher, 1915. G. Habitus, ventral view. H. Habitus, dorsal view. — I–J. Hemisphaerius lysanias Fennah, 1978. I. Habitus, dorsal view. J. Metope and clypeus, facial view. — K–L. Rotundiforma nigrimaculata Meng, Wang & Qin, 2013. K. Habitus, dorsal view. L. Metope and clypeus, facial view. Scale bar = 1 mm.
Fig. 5 in A new green-coloured Lusitanipus Mauriès, 1978 from the Iberian Peninsula (Diplopoda: Callipodida: Dorypetalidae)
Fig. 5. Gonopod of ♂ paratype (MNCN 20.07/2071). A. Posterior view. B. Lateral view. C. Anterior view. D. Distal part of right telopodite in posterior view. E. Tip of right telopodite with tip of solenomerite visible. Scale bars: A–D = 0.4 mm, E = 0.1 mm. Abbreviations: α, β = processes of telopodite; arc = semi-circular arc of gonocoxite; c = gonocoxite; f = pseudoflagellum (or hornflagellum); l = lamella; m = membranous structures; s = solenomerite; sp = subrectangular projection of membranous structures; srp = semi-rectangular process of gonocoxite; t = telopodite.
Fig. 6 in A new green-coloured Lusitanipus Mauriès, 1978 from the Iberian Peninsula (Diplopoda: Callipodida: Dorypetalidae)
Fig. 6. Telopodite and gonocoxite of Lusitanipus alternans and Lusitanipus xanin sp. nov. A. Distal part of gonopod of Lusitanipus alternans in anterior view, redrawn after Reboleira & Enghoff (2015). B. Distal part of gonopod of Lusitanipus xanin sp. nov. in anterior view. C. Tip of telopodite of Lusitanipus alternans in lateral view, redrawn after Verhoeff (1900) (original without scale bar). D. ip of telopodite of Lusitanipus alternans in ventrolateral view, redrawn after a SEM photograph by Reboleira & Enghoff (2015). E. Tip of telopodite of Lusitanipus xanin sp. nov. in lateral view. Scale bars = 0.1 mm. Abbreviations: α, β and γ = processes of telopodite; c = gonocoxite; f = pseudoflagellum (or hornflagellum); l = lamella; s = solenomerite; t = telopodite.
Fig. 4 in A new green-coloured Lusitanipus Mauriès, 1978 from the Iberian Peninsula (Diplopoda: Callipodida: Dorypetalidae)
Fig. 4. Legs of ♂ paratype (MNCN 20.07/2071) seen by optic microscopy. A. Leg 1. B. Leg 2. C. Leg 3. D. Coxa and coxal sac of leg 4. E. Tip of tarsus and claw of leg 4. Scale bars: A–D = 0.5 mm, E =0.1 mm.
Fig. 3 in A new green-coloured Lusitanipus Mauriès, 1978 from the Iberian Peninsula (Diplopoda: Callipodida: Dorypetalidae)
Fig. 3. Morphological details of Lusitanipus xanin sp. nov. A. Head of ♂ paratype (note: colour has faded after 13 years in ethanol) (MNCN 20.07/2071). B. Last antennomeres of ♀ paratype (MNCN 20.07/2070). C. Posterodorsal part of the head of ♀ paratype and collum in dorsal view (MNCN 20.07/2070). D. Dorsal part of pleurotergites 5 (only partially visible) to 7 in lateral view (MNCN 20.07/2070). E. Detail of ventral part of first rings of ♀ in lateral view, with posterior tip of collum and pleurotergite 2 visible, four first pair of legs (second reduced) and coxal sacs (MNCN 20.07/2070). F. Telson and last rings of ♀ paratype (MNCN 20.07/2070). Scale bars = 0.5 mm.
Figs 49‒50. Plutocampa methoria Chevrizov, 1978. 49 in Asian cave-adapted diplurans, with the description of two new genera and four new species (Arthropoda, Hexapoda, Entognatha)
Figs 49‒50. Plutocampa methoria Chevrizov, 1978. 49. Sensillum of the third antennomere. 50. Left labial palp and palpiform process (pp).
Fig. 4. A‒B ‒ Maurodactylus kukuensis V. G. Putshkov, 1978 in Two new species and ten new records of Heteroptera from Turkey, including the first record of the potential alien Campylomma miyamotoi in the Western Palaearctic
Fig. 4. A‒B ‒ Maurodactylus kukuensis V. G. Putshkov, 1978: A ‒ male; B ‒ female. C ‒ Pinalitus viscicola (Puton, 1888), male. D ‒ Platycranus (Genistocapsus) alkestis Linnavuori, 1999, male. Scale bars: 1 mm.
Data from: Long-term persistence of monotypic dengue transmission in small size isolated populations, French Polynesia, 1978-2014
<p>Understanding the transition of epidemic to endemic dengue transmission remains a challenge in regions where serotypes co-circulate and there is extensive human mobility. French Polynesia, an isolated group of 72 inhabited islands, distributed among five geographically separated subdivisions, has recorded mono-serotype epidemics since 1944, with long inter-epidemic periods of circulation. Laboratory confirmed cases have been recorded since 1978, enabling exploration of dengue epidemiology under monotypic conditions in an isolated, spatially structured geographical location. A database was constructed of confirmed dengue cases, geolocated to island for a 35-year period. Statistical analyses of viral establishment, persistence and fade-out as well as synchrony among subdivisions were performed. Seven monotypic and one heterotypic dengue epidemic occurred, followed by low-level viral circulation with a recrudescent epidemic occurring on one occasion. Incidence was asynchronous among the subdivisions. Complete viral die-out occurred on several occasions with invasion of a new serotype, but also in the absence of any novel serotype. Island population size had a strong impact on the establishment, persistence and fade-out of dengue cases and endemicity was estimated achievable only at a population size in excess of 175 000. Despite island remoteness and low population size, dengue cases were observed somewhere in French Polynesia almost constantly, in part due to the spatial structuration generating asynchrony among subdivisions. Long-term persistence of dengue virus in this group of island populations may be enabled by island hopping, although could equally be explained by a reservoir of sub-clinical infections on the most populated island, Tahiti.</p>
FIGURE 1. Trischizostoma denticulatum Ledoyer, 1978 in The genus Trischizostoma (Crustacea: Amphipoda: Trischizostomidae) from the Southwest Atlantic, collected by the REVIZEE Program
FIGURE 1. Trischizostoma denticulatum Ledoyer, 1978, attached to Bathypterois phenax Parr, 1 female, 24 mm, and 1 juvenile, 6 mm, MNRJ 15146.
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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.