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Figure 3 from: El-Sherbiny MM, Al-Harbi MA (2020) New morphological and molecular data on the little-known pontellid Calanopia media Gurney, 1927 (Crustacea, Copepoda, Calanoida) from the Red Sea, with notes on its diel vertical distribution. ZooKeys 922: 13-33. https://doi.org/10.3897/zookeys.922.46977
Figure 3 Calanopia media female from the Red Sea A mandible B maxillule C maxilla D maxilliped. Scale bars in mm.
Figure 6 from: El-Sherbiny MM, Al-Harbi MA (2020) New morphological and molecular data on the little-known pontellid Calanopia media Gurney, 1927 (Crustacea, Copepoda, Calanoida) from the Red Sea, with notes on its diel vertical distribution. ZooKeys 922: 13-33. https://doi.org/10.3897/zookeys.922.46977
Figure 6 SEM micrograph of Calanopia media male from the Red Sea A rostrum, ventral view B prosomal end with abdomen, ventral view (medial notch indicated by arrow) C enlarged segments XX–XXIII D male leg 5, posterior view.
Figure 7 from: El-Sherbiny MM, Al-Harbi MA (2020) New morphological and molecular data on the little-known pontellid Calanopia media Gurney, 1927 (Crustacea, Copepoda, Calanoida) from the Red Sea, with notes on its diel vertical distribution. ZooKeys 922: 13-33. https://doi.org/10.3897/zookeys.922.46977
Figure 7 Neighbor Joining phylogenetic tree based on the mtCOI genes of Calanopia elliptica, C. media, C. minor and C. thompsoni from the Red Sea (indicated by *). Calanopia thompsoni sequences (indicated by +) from GenBank were used for comparative analysis.
Figure 5 from: El-Sherbiny MM, Al-Harbi MA (2020) New morphological and molecular data on the little-known pontellid Calanopia media Gurney, 1927 (Crustacea, Copepoda, Calanoida) from the Red Sea, with notes on its diel vertical distribution. ZooKeys 922: 13-33. https://doi.org/10.3897/zookeys.922.46977
Figure 5 Calanopia media male from the Red Sea A habitus, dorsal view B rostrum, lateral view C enlarged rostral filaments (rudimentary rostral notch indicated by arrow) D abdomen, ventral view (knob indicated by arrow) E right antennule F enlarged segments XVIII–XXIII G leg 5, posterior view. Scale bars in mm.
Figure 1 from: El-Sherbiny MM, Al-Harbi MA (2020) New morphological and molecular data on the little-known pontellid Calanopia media Gurney, 1927 (Crustacea, Copepoda, Calanoida) from the Red Sea, with notes on its diel vertical distribution. ZooKeys 922: 13-33. https://doi.org/10.3897/zookeys.922.46977
Figure 1 Calanopia media female from the Red Sea A habitus, dorsal view B habitus, lateral view C rostrum, lateral view (rudimentary rostral notch indicated by arrow) D abdomen, ventral view E abdomen, dorsal view F–G antennule H antenna. Scale bars in mm.
Figure 4 from: El-Sherbiny MM, Al-Harbi MA (2020) New morphological and molecular data on the little-known pontellid Calanopia media Gurney, 1927 (Crustacea, Copepoda, Calanoida) from the Red Sea, with notes on its diel vertical distribution. ZooKeys 922: 13-33. https://doi.org/10.3897/zookeys.922.46977
Figure 4 Calanopia media female from the Red Sea A leg 1, anterior view B leg 2, anterior view C leg 3, anterior view D leg 4, posterior view E leg 5, posterior view. Scale bars in mm.
Figure 2 from: El-Sherbiny MM, Al-Harbi MA (2020) New morphological and molecular data on the little-known pontellid Calanopia media Gurney, 1927 (Crustacea, Copepoda, Calanoida) from the Red Sea, with notes on its diel vertical distribution. ZooKeys 922: 13-33. https://doi.org/10.3897/zookeys.922.46977
Figure 2 SEM micrographs of Calanopia media female from the Red Sea A rostrum, ventral view B abdomen, dorsal view C abdomen, ventral view D leg 5, posterior view.
Precise distances, masses, ages and 3D velocities of ~140000 red clump stars
<p>We present a sample of $\sim$\,140,000 primary red clump (RC) stars of spectral signal-to-noise ratios higher than 20 from the LAMOST Galactic spectroscopic surveys, selected based on their positions in the metallicity-dependent effective temperature--surface gravity and color--metallicity diagrams, supervised by high-quality $Kepler$ asteroseismology data.<br> The stellar masses and ages of those stars are further determined from the LAMOST spectra, using the Kernel Principal Component Analysis method, trained with thousands of RCs in the LAMOST-$Kepler$ fields with accurate asteroseismic mass measurements. <br> The purity and completeness of our primary RC sample are generally higher than 80\,per cent.<br> For the mass and age, a variety of tests show typical uncertainties of 15 and 30\,per cent, respectively.<br> Using over ten thousand primary RCs with accurate distance measurements from the parallaxes of Gaia\,DR2, we re-calibrate the $K_{\rm s}$ absolute magnitudes of primary RCs by, for the first time, considering both the metallicity and age dependencies.<br> With the the new calibration, distances are derived for all the primary RCs, with a typical uncertainty of 5--10\,per cent, even better than the values yielded by the Gaia parallax measurements for stars beyond 3--4\,kpc.<br> The sample covers a significant volume of the Galactic disk of $4\,\leq\,R\,\leq\,16$\,kpc, $|Z|\,\leq\,5$\,kpc, and $-20\,\leq\,\phi\,\leq\,50^{\circ}$.<br> Stellar atmospheric parameters, line-of-sight velocities and elemental abundances derived from the LAMOST spectra and proper motions of Gaia\,DR2 are also provided for the sample stars.<br> Finally, the selection function of the sample is carefully evaluated in the color-magnitude plane for different sky areas.</p> <p>Details about the table:</p> <p> RA: Right ascension (degrees)<br> DEC: Declination (degrees)<br> GLON: Galactic longitude l (degrees)<br> GLAT: Galactic latitude b (degrees)<br> RV: Line-of-sight velocity (km/s)<br> ERR_RV: Uncertainty of line-of-sight velocity (km/s)<br> TEFF: Effective temperature (K)<br> ERR_TEFF: Uncertainty of effective temperature (K)<br> LOGG: Surface gravity<br> ERR_LOGG: Uncertainty of surface gravity<br> FEH: Metallicity<br> ERR_FEH: Uncertainty of metallicity<br> AFE: Alpha-to-iron abundance<br> ERR_AFE: Uncertainty of apha-to-iron abundance<br> AGE: Stellar age (Gyr)<br> ERR_AGE: Uncertainty of stellar age (Gyr)<br> MASS: Stellar mass (solar mass)<br> ERR_MASS: Uncertainty of stellar mass (solar mass)<br> J: 2MASS J band magnitude<br> ERR_J: Uncertainty of 2MASS J band magnitude<br> H: 2MASS H band magnitude<br> ERR_H: Uncertainty of 2MASS H band magnitude<br> KS: 2MASS Ks band magnitude<br> ERR_KS: Uncertainty of 2MASS Ks band magnitude<br> G: Gaia DR2 G band magnitude<br> ERR_G: Uncertainty of Gaia DR2 G band magnitude<br> BP: Gaia DR2 BP band magnitude<br> ERR_BP: Uncertainty of Gaia DR2 BP band magnitude<br> RP: Gaia DR2 RP band magnitude<br> ERR_RP: Uncertainty of Gaia DR2 RP band magnitude<br> EBV: E (B - V) (mag)<br> MKS: Absolute magnitude in Ks band<br> DISTANCE: distance (kpc)<br> ERR_DISTANCE: Uncertainty of distance (kpc)<br> PARALLAX: Gaia DR2 parallax (mas)<br> ERR_PARALLAX: Uncertainty of Gaia DR2 parallax (mas)<br> PMRA: Proper motion in R.A. (mas/yr)<br> ERR_PMRA: Uncertainty of proper motion in R.A. (mas/yr)<br> PMDEC: Proper motion in Dec. (mas/yr)<br> ERR_PMDEC: Uncertainty of proper motion in Dec. (mas/yr)<br> F_CMD: Selection fraction in color-magnitude diagram</p>
Figure 5 from: Orsenigo S, Bernardo L, Cambria S, Gargano D, Laface VLA, Musarella CM, Passalacqua NG, Spampinato G, Tavilla G, Fenu G (2020) Global and Regional IUCN Red List Assessments: 9. Italian Botanist 9: 111-123. https://doi.org/10.3897/italianbotanist.9.55223
Figure 5 Soldanella calabrella Kress, at Materazzelli (Cosoleto, Reggio Calabria). Photograph by V.L.A. Laface.
Figure 3 from: Orsenigo S, Bernardo L, Cambria S, Gargano D, Laface VLA, Musarella CM, Passalacqua NG, Spampinato G, Tavilla G, Fenu G (2020) Global and Regional IUCN Red List Assessments: 9. Italian Botanist 9: 111-123. https://doi.org/10.3897/italianbotanist.9.55223
Figure 3 Romulea variicolor in the rocky coast near Sampieri (Ragusa, Sicily). Photograph by S. Cambria.
Figure 1 from: Orsenigo S, Bernardo L, Cambria S, Gargano D, Laface VLA, Musarella CM, Passalacqua NG, Spampinato G, Tavilla G, Fenu G (2020) Global and Regional IUCN Red List Assessments: 9. Italian Botanist 9: 111-123. https://doi.org/10.3897/italianbotanist.9.55223
Figure 1 Luzula pindica at Piani di Pollino (Terranova di Pollino, Potenza, Basilicata), a locality included in the Pollino National Park. Photograph by Liliana Bernardo.
Figure 2 from: Orsenigo S, Bernardo L, Cambria S, Gargano D, Laface VLA, Musarella CM, Passalacqua NG, Spampinato G, Tavilla G, Fenu G (2020) Global and Regional IUCN Red List Assessments: 9. Italian Botanist 9: 111-123. https://doi.org/10.3897/italianbotanist.9.55223
Figure 2 Left side: area of occupancy of Luzula pindica in the southern Italian peninsula; right side: location of the AOO cells with respect to the boundaries of the Pollino National Park (light shaded area).
Figure 4 in Zoeal stages of Hiplyra variegata (Rüppell, 1830) (Crustacea: Brachyura: Leucosiidae) reared in the laboratory and collected from plankton at Al-Kharrar creek, central Red Sea
Figure 4. Hiplyra variegata (Rüppell, 1830), pleopod: (a) zoea II; (b) zoea III. Pereiopod: (c) zoea II; (d) zoea III. Dorsal view of pleon: (e) zoea I; (f) zoea II; (g) zoea III. Dorsal view of telson: (h) zoea III.
Figure 3 in Zoeal stages of Hiplyra variegata (Rüppell, 1830) (Crustacea: Brachyura: Leucosiidae) reared in the laboratory and collected from plankton at Al-Kharrar creek, central Red Sea
Figure 3. Hiplyra variegata (Rüppell, 1830), first maxilliped: (a) zoea I; (b) zoea II; (c) zoea III. Second maxilliped: (d) zoea I; (e) zoea II; (f) zoea II; Third maxilliped: (g) zoea III.
Figure 1 in Zoeal stages of Hiplyra variegata (Rüppell, 1830) (Crustacea: Brachyura: Leucosiidae) reared in the laboratory and collected from plankton at Al-Kharrar creek, central Red Sea
Figure 1. Hiplyra variegata (Rüppell, 1830), lateral view of carapace: (a) zoea I; (b) zoea II; (c) zoea III. Dorsal view of rostrum spine: (d) zoea I; (e) zoea II; (f) zoea III. Antennule: (g) zoea I; (i) zoea II; (k) zoea III. Antenna: (h) zoea I; (j) zoea II; (l) zoea III.
Figure 2 in Helminth fauna of the invasive American red-eared slider Trachemys scripta in eastern Spain: potential implications for the conservation of native terrapins
Figure 2. Parasites found in the American red-eared slider, Trachemys scripta in eastern Spain. (A) Telorchis solivagus; (B) Serpinema microcephalus (anterior part detail); (C) Neopolystoma orbiculare (immature); (D) Neopolystoma orbiculare (adult). Scale bars: A, B, D, 1 mm; C, 0.5 mm.
Hidden introductions of freshwater red algae via the aquarium trade exposed by DNA barcodes
<p>The global aquarium trade can introduce alien freshwater invaders, potentially impacting local aquatic ecosystems and their biodiversity. The role of the aquarium trade in spreading freshwater red macroalgae that hitchhike on ornamental aquatic plants and animals is unassessed. We investigated this human-mediated phenomenon via a broad biodiversity survey and genetic analysis of freshwater red algae in the field and aquarium shops in East Asia.</p> <p><b>Results</b><br> We found 26 molecular operational taxonomic units (mOTUs) in Taiwan, some of which are cryptic. Phylogeographical analysis revealed three potential introduced mOTUs in Taiwan, which exhibit no local genetic variation in Taiwan and are distributed across continents. Also, we posit that some presumably endangered freshwater red algae may be preserved in aquaria, an unintentional <i>ex situ</i> conservation site for these organisms that are vulnerable to water pollution from anthropogenic disturbances.</p> <p><b>Main Conclusions</b><br> Collectively, these data suggest that freshwater red algae have been hitchhiking and dispersed via the aquarium trade, an important and overlooked mechanism of introduction of these organisms across the globe.</p>
Figure 2 in Phylogeography of the Eurasian red squirrel (Sciurus vulgaris orientis) on the boreal island of Hokkaido, Japan
Figure 2. Sampling localities of Sciurus vulgaris orientis in two regions (southern and northern) in Hokkaido Island, Japan. Each locality is labelled with numbers corresponding to those identified in Appendix 1. Symbols indicate phylogroups.
Figure 1 in Phylogeography of the Eurasian red squirrel (Sciurus vulgaris orientis) on the boreal island of Hokkaido, Japan
Figure 1. Vegetation zones in Hokkaido Island, Japan: A) present; B) during the last glacial period (after Dobson 1994).
Figure 5 from: Abdel-Dayem MS, Abu El-Ghiet UM, Elsheikh TM, Elgharbawy AA, Al-Fifi ZIA, Aldhafer HM (2020) The first survey of the beetles (Coleoptera) of the Farasan Archipelago of the southern Red Sea, Kingdom of Saudi Arabia. ZooKeys 959: 17-86. https://doi.org/10.3897/zookeys.959.51224
Figure 5 Zoogeographical composition of the beetle fauna of Farasan Archipelago, southern Red Sea, KSA, based on their general distribution. AFR, Afrotropical; AUS, Australian; COS, Cosmopolitan; MAD, Madagascan; ORR, Oriental; PAL, Palaearctic; SAR, Saharo-Arabian; SCO, Subcosmopolitan; SJP, Sino_Japanese.
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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.