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Videos of Gold Nanorods Etching in Graphene Liquid Cell Transmission Electron Microscopy- 34 mM FeCl3
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Feret diameter (mm), area (mm2), and circularity of microplastic debris collected by manta net aboard the Scripps Environmental Accumulation of Plastic Expedition (SEAPLEX) cruise, August 2009, and NOAA Okeanos Explorer expedition, 2010.
Microplastic was collected using a standard manta net tow. Each sample was sorted at 6-12x magnification under a Wild M-5 dissecting microscope, and plastic particles and H. sericeus removed for further analysis. Plastic particles were soaked in deionized water to remove salts, dried at 60°C, and stored in a desiccator. Particles were then digitally imaged with a Zooscan digital scanner (Gilfillan et al. 2009, Gorsky et al. 2010)
Ci-contre: Instantanés sur la biologie de quelques Cigales thaïlandaises 1, Cryptotympana aquila (Walker, 1850), mâle en train de s'alimenter (objectif de 100 mm, en cage). – 2, Cryptotympana mandarina Distant, 1891, femelle achevant sa métamorphose (objectif de 135 mm, in natura, 0 h 45). – 3, Meimuna durga (Distant, 1881); mâle cymbalisant, ailes non écartées (objectif de 135 mm, in natura, 14 h 15). – 4, Meimuna durga (Distant, 1881), mâle et femelle accouplés (objectif de 135 mm, in natura, 13 h 45). – 5, Pomponia linearis (Walker, 1850), mâle au repos (objectif de 135 mm, in natura, le matin, vers 11 heures). – 6 et 7, Tanna ventriroseus n. sp., mâle cymbalisant (6); mâle s'alimentant (7); (objectif de 100 mm, en cage). – 8, Terpnosia nonusaprilis n. sp., mâle cymbalisant, ailes non écartées (objectif de 135 mm, in natura). – 9, Terpnosia nonpareil s n. sp., mâle et femelle accouplés (objectif de 300 mm, in natura, 11 h 55). – 10, Meimuna tavoyana (Distant, 1888), mâle; vue des 3/4 ventraux mettant en évidence la forme et l'écartement de ses opercules (objectif de 100 mm, en cage). – 11, Gaeana cheni Chou & Yao, 1985, mâle achevant de se métamorphoser (objectif de 135 mm, in natura, la nuit, 3 h 17). – 12, Gaeana cheni Chou & Yao, 1985, couple venant de chuter à terre (objectif de 135 mm, 14 h 35). – 13, Ambragaeana ambra Chou & Yao, 1985, mâle dans la phase finale de sa métamorphose, achevant de pigmenter sa livrée (objectif de 135 mm, in natura, au milieu d'une matinée ensoleillée). (Photographies Michel Boulard). in Éthologie sonore et statut acoustique de quelques Cigales thaïlandaises, incluant la description de deux espèces nouvelles (Hemiptera : Auchenorhyncha*, Cicadoidea, Cicadidae)
Ci-contre: Instantanés sur la biologie de quelques Cigales thaïlandaises 1, Cryptotympana aquila (Walker, 1850), mâle en train de s'alimenter (objectif de 100 mm, en cage). – 2, Cryptotympana mandarina Distant, 1891, femelle achevant sa métamorphose (objectif de 135 mm, in natura, 0 h 45). – 3, Meimuna durga (Distant, 1881); mâle cymbalisant, ailes non écartées (objectif de 135 mm, in natura, 14 h 15). – 4, Meimuna durga (Distant, 1881), mâle et femelle accouplés (objectif de 135 mm, in natura, 13 h 45). – 5, Pomponia linearis (Walker, 1850), mâle au repos (objectif de 135 mm, in natura, le matin, vers 11 heures). – 6 et 7, Tanna ventriroseus n. sp., mâle cymbalisant (6); mâle s'alimentant (7); (objectif de 100 mm, en cage). – 8, Terpnosia nonusaprilis n. sp., mâle cymbalisant, ailes non écartées (objectif de 135 mm, in natura). – 9, Terpnosia nonpareil s n. sp., mâle et femelle accouplés (objectif de 300 mm, in natura, 11 h 55). – 10, Meimuna tavoyana (Distant, 1888), mâle; vue des 3/4 ventraux mettant en évidence la forme et l'écartement de ses opercules (objectif de 100 mm, en cage). – 11, Gaeana cheni Chou & Yao, 1985, mâle achevant de se métamorphoser (objectif de 135 mm, in natura, la nuit, 3 h 17). – 12, Gaeana cheni Chou & Yao, 1985, couple venant de chuter à terre (objectif de 135 mm, 14 h 35). – 13, Ambragaeana ambra Chou & Yao, 1985, mâle dans la phase finale de sa métamorphose, achevant de pigmenter sa livrée (objectif de 135 mm, in natura, au milieu d'une matinée ensoleillée). (Photographies Michel Boulard).
Supplementary material 1 from: Galasso G, Domina G, Andreatta S, Angiolini C, Ardenghi NMG, Aristarchi C, Arnoul M, Azzella MM, Bacchetta G, Bartolucci F, Bodino S, Bommartini G, Bonari G, Buono S, Buono V, Caldarella O, Calvia G, Corti E, D'Antraccoli M, De Luca R, De Mattia F, Di Natale S, Di Turi A, Esposito A, Ferretti G, Fiaschi T, Fogu MC, Forte L, Frigerio J, Gubellini L, Guzzetti L, Hofmann N, Laface VLA, Laghetti G, Lallai A, La Rosa A, Lazzaro L, Lodetti S, Lonati M, Luchino F, Magrini S, Mainetti A, Marignani M, Maruca G, Medagli P, Mei G, Menini F, Mezzasalma V, Misuri A, Mossini S, Mugnai M, Musarella CM, Nota G, Olivieri N, Padula A, Pascale M, Pasquini F, Peruzzi L, Picella G, Pinzani L, Pirani S, Pittarello M, Podda L, Enri SR, Rifici CD, Roma-Marzio F, Romano R, Rosati L, Scafidi F, Scarici E, Scarici M, Spampinato G, Stinca A, Wagensommer RP, Zanoni G, Nepi C (2019) Notulae to the Italian alien vascular flora: 8. Italian Botanist 8: 63-93. https://doi.org/10.3897/italianbotanist.8.48621
: Data type: species data
Figure 4 from: Hofmann MM, Renner SS (2020) One-year-old flower strips already support a quarter of a city's bee species. Journal of Hymenoptera Research 75: 87-95. https://doi.org/10.3897/jhr.75.47507
Figure 4 The percentage of bee species recorded at each flower strip that is also found in the surrounding area at distances of 500, 1000, and 1500 m.
Supplementary material 3 from: Hofmann MM, Renner SS (2020) One-year-old flower strips already support a quarter of a city's bee species. Journal of Hymenoptera Research 75: 87-95. https://doi.org/10.3897/jhr.75.47507
: Data type: species data
Figure 2 from: Hofmann MM, Renner SS (2020) One-year-old flower strips already support a quarter of a city's bee species. Journal of Hymenoptera Research 75: 87-95. https://doi.org/10.3897/jhr.75.47507
Figure 2 The flower strip at Fockensteinstraße as an example of the urban context of the flower strips studied here.
Figure 1 from: Hofmann MM, Renner SS (2020) One-year-old flower strips already support a quarter of a city's bee species. Journal of Hymenoptera Research 75: 87-95. https://doi.org/10.3897/jhr.75.47507
Figure 1 The nine flower strips monitored for this study (modified from https://www.openstreetmap.org, using QGIS 3.8.2 (QGIS Development Team 2019) and Munich's bee records (sightings and/or specimens) between 1997 and 2017.
Figure 3 from: Hofmann MM, Renner SS (2020) One-year-old flower strips already support a quarter of a city's bee species. Journal of Hymenoptera Research 75: 87-95. https://doi.org/10.3897/jhr.75.47507
Figure 3 Numbers of species and individuals recorded between 1997 and 2017 within a radius of 500, 1000, and 1500 m from the centre of the respective flower strip (compare Fig. 1). For details of how past recordings were made see Materials and Methods.
Supplementary material 1 from: Hofmann MM, Renner SS (2020) One-year-old flower strips already support a quarter of a city's bee species. Journal of Hymenoptera Research 75: 87-95. https://doi.org/10.3897/jhr.75.47507
: Data type: species data
Supplementary material 2 from: Hofmann MM, Renner SS (2020) One-year-old flower strips already support a quarter of a city's bee species. Journal of Hymenoptera Research 75: 87-95. https://doi.org/10.3897/jhr.75.47507
: Data type: accession numbers
METHODS. Bovine ilia were used in the simulations because their histological structure (a fibrolamellar cortex overlying cancellous bone26) was found to match that of the Triceratops ilium. Bone sections 10 x 50 x 縠 3.0 cm with cortices ranging from 0.5 to 5.5 mm in depth (the range of initial cortical-thickness estimates based on gross morphology) were mounted on a servohydraulic mechanical loading frame (MTS Bionix, Minneapolis) and penetrated with an aluminium-bronze T. rex tooth replica. The replica was cast from an actual adult T. rex maxillary tooth, after casts made from some ofthe deeper bite marks revealed the size and shape of the teeth that had impacted the pelvis8 • The replica was penetrated into the ilia sections at 1 mm s-1 to a depth of 11.5 mm, equivalent to the maximum depth of the deepest ilium bite mark8 • Forces were measured with an MTS 25 N strain-gauge-based axial load cell accurate to 0.2%. The forces increased with increasing penetration depth even after the cortical layer had been perforated and the underlying cancellous bone was being crushed. The increase in force with penetration depth is attributed to a greater cortical surface area coming into contact with the semi-conical penetrator tooth as it descended through the ilia. in Bite-force estimation for Tyrannosaurus rex from tooth-marked bones
METHODS. Bovine ilia were used in the simulations because their histological structure (a fibrolamellar cortex overlying cancellous bone26) was found to match that of the Triceratops ilium. Bone sections 10 x 50 x 縠 3.0 cm with cortices ranging from 0.5 to 5.5 mm in depth (the range of initial cortical-thickness estimates based on gross morphology) were mounted on a servohydraulic mechanical loading frame (MTS Bionix, Minneapolis) and penetrated with an aluminium-bronze T. rex tooth replica. The replica was cast from an actual adult T. rex maxillary tooth, after casts made from some ofthe deeper bite marks revealed the size and shape of the teeth that had impacted the pelvis8 • The replica was penetrated into the ilia sections at 1 mm s-1 to a depth of 11.5 mm, equivalent to the maximum depth of the deepest ilium bite mark8 • Forces were measured with an MTS 25 N strain-gauge-based axial load cell accurate to 0.2%. The forces increased with increasing penetration depth even after the cortical layer had been perforated and the underlying cancellous bone was being crushed. The increase in force with penetration depth is attributed to a greater cortical surface area coming into contact with the semi-conical penetrator tooth as it descended through the ilia.
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.
FIGURE1. Lateral view of Siphamia guttulata (CSIRO H 6930-02, 25 mm SL). Scale bar = 5 mm. in Redescription and distributional range extension of the Speckled Siphonfish, Siphamia guttulata (Pisces: Apogonidae)
FIGURE1. Lateral view of Siphamia guttulata (CSIRO H 6930-02, 25 mm SL). Scale bar = 5 mm.
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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.