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611 results for “eastern North America”
Figure 8 in Two unusual new species of Caleremaeus (Acari: Oribatida) from eastern North America, with redescription of C. retractus and reevaluation of the genus
Figure 8 Caleremaeus arboricolusn. sp., adult: A – dorsal view (legs mostly omitted); B – ventral view (legs omitted). Scale bar: 50 µm.
Figure 1 in Two unusual new species of Caleremaeus (Acari: Oribatida) from eastern North America, with redescription of C. retractus and reevaluation of the genus
Figure 1 Caleremaeus retractus(Banks), adult: A – dorsal view (legs mostly omitted); B – lateral view (gnathosoma, legs and anal, genital plates omitted); C – subcapitulum, ventral view (adoral lips and palps omitted); D – palp, abaxial view. Scale bars: 50 µm (A, B); 10 µm (C, D).
Figure 2 in Two unusual new species of Caleremaeus (Acari: Oribatida) from eastern North America, with redescription of C. retractus and reevaluation of the genus
Figure 2 Caleremaeus retractus(Banks), transmitted-light micrographs of near-topotypical adults: A – dorsolateral view; B – posterior view; C – cerotegument separated from notogaster, lateral view; D – same, dorsal view (face-on); E – bothridium and bothridial seta (head face-on); F – optical sections of bothridium; upper image focused fine circular striations of inner chamber, lower image on longitudinal striations of deepest part of inner chamber; G – anterior region of prodorsum, dorsal view (insert = enlargement of seta le, arrow to break in seta emphasizing surrounding cerotegument nodule); H – same, different specimen, showing cusp variation; I – anterior region of specimen in G, deeper focus showing rostral bulge and submarginal crest; J – prodorsum, dorsolateral view (gnathosoma removed; setaele and ro represented only by birefringent core); K – specimen in J, deeper focus on rostral bulge (arrowhead to transverse striae of embossed pattern on inner surface of rostral bulge; L – rostral region of dissected specimen, anterior view (black arrow to central ridge of embossed pattern on inner face of rostral bulge); M – parasagittal section of prodorsum and anterior hysterosoma (insert = enlarged base of rostral bulge and rostrophragma). Scale bars: 50 µm (A, B); 20 µm (J, M); 10 µm (E, G-I, K, L); 5 µm (C, D, F).
Figure 9 in Two unusual new species of Caleremaeus (Acari: Oribatida) from eastern North America, with redescription of C. retractus and reevaluation of the genus
Figure 9 Caleremaeus arboricolusn. sp., transmitted-light micrographs of adult: A – anterior third, dorsal view; B – transverse ridge and setae le; C – same, different specimen; D – bothridium and setabs; E – posterolateral area of prodorsum, dorsal view; F – head of bothridial seta; G – prodorsum, lateral view; H – same, deep focus optical section (insert on left = enlarged base of rostral bulge and rostrophragma); I – middle third of body, lateral view; J – notogastral seta h2; K – notogastral seta lp; L – notogastral setae p1 and p3; M – posterior view (setae h1, p1 broken from alveolus). Scale bars: 20 µm (A, G-I, M); 10 µm (B, C); 5 µm (D-F, J-L).
Figure 7 in Two unusual new species of Caleremaeus (Acari: Oribatida) from eastern North America, with redescription of C. retractus and reevaluation of the genus
Figure 7 Caleremaeus retractus(Banks), transmitted-light micrographs of near-topotypical juveniles: A – protonymph, dorsal view (setae h1 incomplete); B – same, lateral view of posterior hysterosoma; C – deutonymph, lateral view of hysterosoma; D – tritonymph, dorsal view (insert = right lamellar seta and cusp); E – same, lateral view of hysterosoma; F – tritonymph, ventral view of prodorsal margin and partial gnathosoma (upper right insert = enlarged seta ro); G – gastronotic cornicle of tritonymph (scalps removed); H – bothridial seta of deutonymph; I – gastronotal seta lm from tritonymph (arrow to basal cerotegument nodule); J – same, but seta h2; K – same, but seta p2; L – dorsodistal process of tibia I, tritonymph, distal to left (φ1 rising out of focus; insert = opposite side of seta d, showing faint barbs); M – tibia, genu and distal part of femur I from tritonymph, adaxial view; N – coupled seta d and solenidion on tibia II (distal to left). Dots in B, C, E indicate that labeled seta (or its insertion) is on exuvial scalp of larva (.), protonymph (..) or deutonymph (…). Scale bars: 50 µm (D); 20 µm (A-C, E); 10 µm (M); 5 µm (F-H, L, N); 2 µm (I-K).
Data and code associated with "Evaluating the definition and distribution of spring ephemeral wildflowers in eastern North America"
<p>Data and code associated with a paper by Yancy et al titled "Evaluating the definition and distribution of spring ephemeral wildflowers in eastern North America". Metadata is included in files when possible.</p>
Figures 22–23 in Bees of the genera Dufourea and Dieunomia of Michigan (Hymenoptera: Apoidea: Halictidae), with a key to the Dufourea of eastern North America
Figures 22–23. Lateral habitus of Dieunomia heteropoda (Say). 22. Female. 23. Male. Images courtesy of Laurence Packer.
Figures 10–15 in Bees of the genera Dufourea and Dieunomia of Michigan (Hymenoptera: Apoidea: Halictidae), with a key to the Dufourea of eastern North America
Figures 10–15. Males of Dufourea novaeangliae (Robertson) (10–12) and D. monardae (Viereck) (13–15). 10, 13. Propodea. 11, 14. Metatrochanters. 12, 15. Metasomal sterna six. Modified from Dumesh & Sheffield (2012).
Figures 6–9 in Bees of the genera Dufourea and Dieunomia of Michigan (Hymenoptera: Apoidea: Halictidae), with a key to the Dufourea of eastern North America
Figures 6–9. Females of Dufourea novaeangliae (Robertson) (6, 7) and D. monardae (Viereck) (8, 9). 6, 8. Head and mouthparts in lateral view. 7, 9. Mesobasitarsi. Modified from Dumesh & Sheffield (2012).
Figures 4–5 in Bees of the genera Dufourea and Dieunomia of Michigan (Hymenoptera: Apoidea: Halictidae), with a key to the Dufourea of eastern North America
Figures 4–5. Faces of female Dufourea Lepeletier de Saint Fargeau. 4. Dufourea novaeangliae (Robertson). 5. D. harveyi (Cockerell). Modified from Dumesh & Sheffield (2012).
Figures 2–3 in Bees of the genera Dufourea and Dieunomia of Michigan (Hymenoptera: Apoidea: Halictidae), with a key to the Dufourea of eastern North America
Figures 2–3. Lateral habitus of male Dufourea Lepeletier de Saint Fargeau. 2. Dufourea maura (Cresson). 3. D. harveyi (Cockerell). Modified from Dumesh & Sheffield (2012).
Figure 1 in Bees of the genera Dufourea and Dieunomia of Michigan (Hymenoptera: Apoidea: Halictidae), with a key to the Dufourea of eastern North America
Figure 1. Face of female Dufourea maura (Cresson). Modified from Dumesh & Sheffield (2012). Scale bar = 1 mm.
WRF output. Resolution: 12 km. Domain: Eastern North America
<p>Derived products from WRF simulations at 12 km resolution. LBC: ERA-Interim. Output every 10-min. Output level: 3rd model level </p> <p>Details given in: Pryor S.C. et al. (2018): Inter-annual variability of wind climates and wind turbine annual energy production. Manuscript published in Wind Energy Science.</p> <p>5 netcdf files;</p> <p>Pryoretal_WES2018_part1.nc contains information shown in Figure 3. Included variables; lat, lng, medianWSHH, CI(medianWSHH), vectors of data in WT grid cells and in grid cells without WT.</p> <p>Pryoretal_WES2018_part2.nc contains information shown in Figure 4. Included variables; Weibull distribution fits by wind speed bin and year, and FFT of output from TX, IA, and NY.</p> <p>Pryoretal_WES2018_part3.nc contains information shown in Figure 5. Included variables; lat, lng, 50th and 90th percentile WI, AEP and difference, vectors of data in WT grid cells and in grid cells without WT.</p> <p>Pryoretal_WES2018_part4.nc contains information shown in Figure 6.Included variables; lat, lng, 50th and 90th percentile AEP and difference, vectors of data in WT grid cells and in grid cells without WT.</p> <p>Pryoretal_WES2018_part5.nc contains information shown in Figure 7. Included variables; lat, lng, time of minimum, time of maximum.</p> <p> </p>
WRF-Chem output. Resolution: 24 km. Domain: Eastern North America
<p>Derived products from WRF-Chem simulations at 24 km resolution.</p> <p>Details given in: Crippa P. et al. (2019): Sensitivity of simulated aerosol properties over eastern North America to WRF-Chem parameterizations. Manuscript published in the Journal of Geophysical Research.</p> <p>14 netcdf files:</p> <p>Crippaetal_JGR2019_AOD.nc contains monthly mean AOD cloud screened for each ensemble member.</p> <p>Crippaetal_JGR2019_net_radiation.nc contains monthly mean surface net radiation for each ensemble member.</p> <p>Crippaetal_JGR2019_NO3_fine.nc contains monthly mean NO3 in the fine aerosol mode for each ensemble member.</p> <p>Crippaetal_JGR2019_SO4_fine.nc contains monthly mean SO4 in the fine aerosol mode for each ensemble member.</p> <p>Crippaetal_JGR2019_PM25_daily.nc contains daily PM<sub>2.5 </sub>concentrations for each ensemble member.</p> <p>Crippaetal_JGR2019_O3_daily.nc contains daily mean surface ozone concentrations in the fine aerosol mode for each ensemble member.</p> <p>Crippaetal_JGR2019_PBLH.nc contains monthly mean planetary boundary layer height for each ensemble member regridded on the MERRA-2 resolution</p> <p>Crippaetal_JGR2019_T2.nc contains monthly mean surface temperature at 2m for each ensemble member regridded on the MERRA-2 resolution</p> <p>Crippaetal_JGR2019_QPBL.nc contains monthly mean specific humidity in the PBL for each ensemble member regridded on the MERRA-2 resolution</p> <p>Crippaetal_JGR2019_PPT.nc contains monthly total precipitation for each ensemble member regridded on the MERRA-2 resolution</p> <p>Crippaetal_JGR2019_lat_WRF-Chem.nc contains the latitude coordinates of the WRF-Chem grid</p> <p>Crippaetal_JGR2019_lon_WRF-Chem.nc contains the longitude coordinates of the WRF-Chem grid</p> <p>Crippaetal_JGR2019_lat_MERRA2.nc contains the latitude coordinates of the MERRA2 grid</p> <p>Crippaetal_JGR2019_on_MERRA2.nc contains the longitude coordinates of the MERRA2 grid</p>
Fig.2. A in Post-extinction survivor fauna from the lowermost Famennian of eastern North America
Fig.2. A.StratigraphicintervalinupperHanoverShaleatGladeCreekthatcontainsUpperKellwasserInterval,Frasnian–Famennianboundary,andbrachiopod bed. Rose diagram is orientation of long axis of lingulid (Barroisella) valves on the bedding surface. Numbers to the right of the stratigraphic section denote bad thickness (in cm). B. Photograph of brachiopod−bearing bedding surface showing partially exfoliated ventral valves of the chonetid brachiopod Retichonetes aff. R. obscurus. C. Cross section of brachiopod−rich horizon. The dark band in the center of the cross section is pyrite−rich.
Fig. 4 in Post-extinction survivor fauna from the lowermost Famennian of eastern North America
Fig. 4. Brachiopods from the shell bed in the Hanover Shale Member of the Java Formation. A–D. Retichonetes aff. S. obscurus Cooper and Dutro, 1982. A. Internal mold of dorsal valve, NYSM 15704 with low medial myophragm, simple sockets flanking the pit near base of cardinal process, × 5.4. B. Upper exteriorviewofdorsalvalve,NYSM15710,×4.8. C.Internalmoldofdorsalvalve,NYSM15705,×7. D.Ventralvalveshowingcostellaewithcrushedand distorted ventral valve of Ambocoelia cf. A. gregaria in upper left, NYSM 15718, × 3.3. E. Tylothyris mesacostalis (Hall, 1867), view of dorsal valve showing centric lamellose ornament and central groove on fold, NYSM 15711, × 2.3. F, G. Praewaagenoconcha speciosa (Hall, 1867). F. Internal mold of dorsal valve with impression of medial myophragm and rugae along the postero−lateral margin, NYSM 15706, × 1.7. G. External mold of dorsal valve showing radial spine bases with some exfoliated shell material, NYSM 15695, × 1.5. H, I. Cyrtospirifer hornellensis Greiner, 1957. H. Exfoliated dorsal valve showing extended postero−lateral extremity, NYSM 15692. I. Ventral valve, NYSM 15691; both × 1.8. J. Ambocoelia cf. A. gregaria Hall, 1867, upper view of flattened dorsal valve showing dorsal groove, NYSM 15719 × 3.5.
Fig. 3 in Post-extinction survivor fauna from the lowermost Famennian of eastern North America
Fig. 3. Brachiopod fauna of the shell bed in upper Hanover Shale Member of the Java Formation. A. Schizophoria (S.) sp. upper view of exfoliated ventral valve, NYSM 15701, × 1.7. B–D. Thiemella leonensis (Hall, 1867). B. Dorsal valve of juvenile specimen, NYSM 15722, × 4.6. C. Ventral valve, NYSM 15694,×2. D.Ventralviewofnearlycompleteshellextractedfrommoldiccavitytoleft,NYSM15699,×2.2.E, F. Ripidiorhynchus?sp. E.Upperviewofventralvalvewithplicaextendingfromanteriormargintobeakofvalve,NYSM15723,×2. F.Partialventralvalveshowingmedialandleftlateralflankplications, NYSM15724,×2. G. Chapinella?sp.,ventralvalvewithlateralplicationsnearshellmargin,NYSM15727,×2. H.Genusandspeciesuncertain,ventralvalve withradialplicaextendingfromanteriorandlateralmarginstobeakofNYSM15728,×4. I, J. Praewaagenoconcha speciosa (Hall,1867). I.Interiorofdorsal valve showing bilobed cardinal process, NYSM 15696, × 2. J. Upper view of ventral valve showing quincuncially arranged spines, NYSM 15697, × 2.
Table 1 in Two unusual new species of Caleremaeus (Acari: Oribatida) from eastern North America, with redescription of C. retractus and reevaluation of the genus
<p><b>Table 1</b> Ontogeny of leg setae and solenidia in <i>Caleremaeus</i> species 1, 2.</p><table><tbody><tr><th></th><th>Trochanter</th><th>Femur</th><th>Genu</th><th>Tibia</th><th>Tarsus</th></tr><tr><th>Leg I</th></tr></tbody><tbody><tr><th>Larva</th><td><i>-</i></td><td><i>d, bv"</i></td><td><i>(l), dσ</i></td><td><i>(l), v', dφ</i> 1</td><td><i>(ft), (tc), (p), (u), (a), s, (pv), (pl), e, ω</i> 1</td></tr><tr><th>Protonymph</th><td><i>-</i></td><td><i>-</i></td><td><i>-</i></td><td><i>-</i></td><td><i>ω</i> 2</td></tr><tr><th>Deutonymph</th><td><i>-</i></td><td><i>(l)</i></td><td><i>-</i></td><td><i>φ</i> 2</td><td><i>-</i></td></tr><tr><th>Tritonymph</th><td><i>v'</i></td><td><i>-</i></td><td><i>v'</i></td><td><i>v"</i></td><td><i>(it)</i></td></tr><tr><th>Adult</th><td><i>-</i></td><td><i>-</i></td><td>[<i>d</i> lost]</td><td>[<i>d</i> lost]</td><td><i>v', l"</i></td></tr><tr><th>Leg II</th><td></td><td></td><td></td><td></td><td></td></tr><tr><th>Larva</th><td><i>-</i></td><td><i>d, bv"</i></td><td><i>(l), dσ</i></td><td><i>l', v', dφ</i></td><td><i>(ft), (tc), (p), (u), (a), s, (pv), ω</i></td></tr><tr><th>Protonymph</th><td><i>-</i></td><td><i>-</i></td><td><i>-</i></td><td><i>-</i></td><td><i>-</i></td></tr><tr><th>Deutonymph</th><td><i>-</i></td><td><i>(l)</i></td><td><i>-</i></td><td><i>l"</i></td><td><i>-</i></td></tr><tr><th>Tritonymph</th><td><i>v'</i></td><td><i>-</i></td><td><i>-</i></td><td><i>v"</i></td><td><i>-</i></td></tr><tr><th>Adult</th><td><i>-</i></td><td><i>-</i></td><td>[<i>d</i> lost]</td><td>[<i>d</i> lost]</td><td><i>l"</i>, (<i>it</i>)</td></tr><tr><th>Leg III</th><td></td><td></td><td></td><td></td><td></td></tr><tr><th>Larva</th><td><i>-</i></td><td><i>d, ev'</i></td><td><i>l’, dσ</i></td><td><i>v', dφ</i></td><td><i>(ft), (tc), (p), (u), (a), s, (pv)</i></td></tr><tr><th>Protonymph</th><td><i>-</i></td><td><i>-</i></td><td><i>-</i></td><td><i>-</i></td><td><i>-</i></td></tr><tr><th>Deutonymph</th><td><i>v', l’</i></td><td><i>l'</i></td><td><i>-</i></td><td><i>l'</i> 3</td><td><i>-</i></td></tr><tr><th>Tritonymph</th><td><i>-</i></td><td><i>-</i></td><td><i>-</i></td><td><i>l'</i> 3, <i>v"</i></td><td><i>-</i></td></tr><tr><th>Adult</th><td><i>-</i></td><td><i>-</i></td><td>[<i>d</i> lost]</td><td>[<i>d</i> lost]</td><td><i>it"</i></td></tr><tr><th>Leg IV</th><td></td><td></td><td></td><td></td><td></td></tr><tr><th>Protonymph</th><td><i>-</i></td><td><i>-</i></td><td><i>-</i></td><td><i>-</i></td><td><i>ft", (p), (u), (pv)</i></td></tr><tr><th>Deutonymph</th><td><i>-</i></td><td><i>d, ev'</i></td><td><i>d, l'</i></td><td><i>v', dφ</i></td><td><i>(瑣), a",</i></td></tr><tr><th>Tritonymph</th><td><i>v'</i></td><td><i>-</i></td><td><i>-</i></td><td><i>l', v"</i></td><td><i>-</i></td></tr><tr><th>Adult</th><td><i>-</i></td><td><i>-</i></td><td><i>-</i></td><td>[<i>d</i> lost]</td><td>-</td></tr></tbody></table><p><sup>1</sup> Adult data are based on all studied species and populations, including <i>C. monilipes</i> from Sweden, Germany and Spain. Ontogenetic data are from <i>C. arboricolus</i> <b>n. sp.</b> (topotypical population), <i>C. retractus</i> (near-topotypical population), a species in the ‘retractus group’ (New York population; see text), and <i>C. monilipes</i> (Norwegian population; see Seniczak and Seniczak 2019 and corrections in R12); from each population all instars were studied, except no larva was available from the <i>C. retractus</i> near-topotypical population.</p><p><sup>2</sup> Setae (Roman letters) and solenidia (<i>σ, φ, ω</i>) are shown where they are first added and are assumed present through the rest of ontogeny, unless noted in brackets. Setae in parentheses represent pseudosymmetrical pairs; dash indicates no addition; underline indicates solenidion is coupled to seta <i>d</i>, in same alveolus.</p><p><sup>3</sup> Seta <i>l'</i> of tibia III is invariably deutonymphal in <i>C. arboricolus</i>, <i>C. retractus</i> and the ‘retractus group’ from New York. By contrast, in <i>C. monilipes l'</i> first forms along with <i>v"</i> in the tritonymph, according to Seniczak and Seniczak (2019); appropriately, <i>l'</i> is absent from both tibiae III of our single deutonymph from Sweden.</p>
Linked collectors and determiners for: Japeaeiella dollŋpartoniana, a New Widespread Lichen in the Appalachian Mountains of Eastern North America.
Natural history specimen data linked to collectors and determiners held within, "Japeaeiella dollŋpartoniana, a New Widespread Lichen in the Appalachian Mountains of Eastern North America". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/feb4164b-2c9c-4da6-acb3-326e2a5a34f2">https://bionomia.net/dataset/feb4164b-2c9c-4da6-acb3-326e2a5a34f2</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/feb4164b-2c9c-4da6-acb3-326e2a5a34f2">https://gbif.org/dataset/feb4164b-2c9c-4da6-acb3-326e2a5a34f2</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: New Syrphidae (Diptera) of North-eastern North America.
Natural history specimen data linked to collectors and determiners held within, "New Syrphidae (Diptera) of North-eastern North America". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/dfc600bf-7410-4aa9-81c2-b3cc9415c989">https://bionomia.net/dataset/dfc600bf-7410-4aa9-81c2-b3cc9415c989</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/dfc600bf-7410-4aa9-81c2-b3cc9415c989">https://gbif.org/dataset/dfc600bf-7410-4aa9-81c2-b3cc9415c989</a>. Formatted as a Frictionless Data package.
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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.