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18,820 results for “northing”
Linked collectors and determiners for: Review of the tribes Sogdini and Leiodini from Japan and North Chishima Islands. Part II. Genera Hydnobius and Leiodes (Coleoptera: Leiodidae).
Natural history specimen data linked to collectors and determiners held within, "Review of the tribes Sogdini and Leiodini from Japan and North Chishima Islands. Part II. Genera Hydnobius and Leiodes (Coleoptera: Leiodidae)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/59fc10fe-e8c3-4537-abb9-049fbda4c7ed">https://bionomia.net/dataset/59fc10fe-e8c3-4537-abb9-049fbda4c7ed</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/59fc10fe-e8c3-4537-abb9-049fbda4c7ed">https://gbif.org/dataset/59fc10fe-e8c3-4537-abb9-049fbda4c7ed</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: Bombus johanseni, a valid North American bumble bee species.
Natural history specimen data linked to collectors and determiners held within, "Bombus johanseni, a valid North American bumble bee species". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/90d8babc-685f-449e-a4ec-7275ca7655c7">https://bionomia.net/dataset/90d8babc-685f-449e-a4ec-7275ca7655c7</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/90d8babc-685f-449e-a4ec-7275ca7655c7">https://gbif.org/dataset/90d8babc-685f-449e-a4ec-7275ca7655c7</a>. Formatted as a Frictionless Data package.
Linked collectors and determiners for: The millipede family Conotylidae in northwestern North America, with a complete bibliography of the family (Diplopoda, Chordeumatida, Heterochordeumatidea, Conotyloidea).
Natural history specimen data linked to collectors and determiners held within, "The millipede family Conotylidae in northwestern North America, with a complete bibliography of the family (Diplopoda, Chordeumatida, Heterochordeumatidea, Conotyloidea)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/f7974bcf-11e7-4d1b-b09d-530dc2dbd54f">https://bionomia.net/dataset/f7974bcf-11e7-4d1b-b09d-530dc2dbd54f</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/f7974bcf-11e7-4d1b-b09d-530dc2dbd54f">https://gbif.org/dataset/f7974bcf-11e7-4d1b-b09d-530dc2dbd54f</a>. Formatted as a Frictionless Data package.
North Atlantic average sea-surface temperature in a CMIP6 multi-model ensemble of historical and ssp585/ssp245 simulations
<p>This dataset contains North Atlantic average sea-surface temperatures and derived indices calculated for a multi-model ensemble of historical and future scenario (ssp585, ssp245) simulations contributing to the Coupled Model Intercomparison Project phase 6. A detailed description of the dataset is provided by Zanchettin, D., and Rubino, A., Accelerated North Atlantic surface warming reshapes the Atlantic Multidecadal Variability, Communications Earth & Environment, 2024, doi:10.1038/s43247-024-01804-x.</p> <p><br>The data are provided as netcdf files.</p> <p>The name of each file is structured as {model}_r{realization}_historical_{scenario}.nc where {model} is the model name, {realization} is a number corresponding to the historical realization, and {scenario} is either of the two scenarios considered (ssp585 and ssp245).</p> <p>Each file contains data for the following one dimensional variables:</p> <ul> <li>year: the sequence of years for which the data are provided</li> <li>NASST: annual-average spatially averaged North Atlantic sea-surface temperature</li> <li>state: slowly variable component of NASST obtained from a dlm decomposition of NASST</li> <li>strend: stochastic trend of NASST obtained from a dlm decomposition of NASST</li> <li>AMV: Atlantic Multidecadal Varibility index obtained as difference between NASST and state</li> </ul> <p> </p>
Data for "Temporal and vertical variability in phytoplankton primary production and microbial community respiration in the North Pacific Subtropical Gyre"
<p>This ALOHA_GOP&R.xslx data set provides measurements of biological rates conducted between April 2015 and July 2020 at different depths in the euphotic zone at or in the vicinity of Station ALOHA (22° 45' N, 158° W), the long-term sampling site of the Hawaii Ocean Time-series (HOT) program, within the North Pacific Subtropical Gyre. </p> <p>The file ALOHA_GOP&R.xslx contains incubation-based measurements of gross oxygen production and community respiration that were measured in the same incubation bottles by applying the <sup>18</sup>O-water method and tracking net changes in oxygen to argon ratios during dawn to dusk in situ incubations, following Ferrón et al. (2016). The samples were measured using membrane inlet mass spectrometry. Rates were measured at 6 depths within the euphotic zone: 5, 25, 45, 75, 100, 125 m, except in a few occasions in which there were no measurements made at 125 m.</p> <p>Data description</p> <table> <tbody> <tr> <td> <p>Variable</p> </td> <td> <p>Description</p> </td> <td> <p>Units</p> </td> </tr> <tr> <td> <p>Date </p> </td> <td> <p>Date of sampling and start of incubation (UTC -10 hours)</p> </td> <td> <p> </p> </td> </tr> <tr> <td> <p>Cruise ID</p> </td> <td> <p>Cruise identification</p> </td> <td> <p>#</p> </td> </tr> <tr> <td> <p>Latitude</p> </td> <td> <p>Latitude</p> </td> <td> <p>degrees N</p> </td> </tr> <tr> <td> <p>Longitude</p> </td> <td> <p>Longitude</p> </td> <td> <p>degrees E</p> </td> </tr> <tr> <td>Stn ALOHA </td> <td>Whether the data are from Station ALOHA (yes/no)</td> <td> </td> </tr> <tr> <td>IncT</td> <td> <p>Incubation time</p> </td> <td> <p>hours</p> </td> </tr> <tr> <td> <p>Depth</p> </td> <td>Nominal depth of sampling and incubation </td> <td> <p>meters</p> </td> </tr> <tr> <td>GOP</td> <td>Gross oxygen production </td> <td>mmol O<sub>2</sub> m<sup>-3</sup> d<sup>-1</sup></td> </tr> <tr> <td>CR</td> <td>Estimate of community respiration </td> <td>mmol O<sub>2</sub> m<sup>-3</sup> d<sup>-1</sup></td> </tr> <tr> <td> <p>Flag GOP</p> </td> <td>Flag identification for gross oxygen production (good=1,questionable=2)</td> <td> <p>#</p> </td> </tr> <tr> <td> <p>Flag CR</p> </td> <td> <p>Flag identification for community respiration (good=1,questionable=2)</p> </td> <td> <p>#</p> </td> </tr> </tbody> </table> <p> </p> <p>The Light-dark_ALOHA_rates.xlsx file contains metabolic rates measured by the ligth-dark oxygen method between June 2005 and June 2007 at different depths in the euphotic zone at Station ALOHA (22° 45' N, 158° W). Rates of net community production, communnity respiration, and gross oxygen production were measured at 6 depths within the euphotic zone (5, 25, 45, 75, 100, 125 m) in dawn to dawn incubations, following Williams et al. (2004). </p> <p>Data description</p> <table> <tbody> <tr> <td> <p>Variable</p> </td> <td> <p>Description</p> </td> <td> <p>Units</p> </td> </tr> <tr> <td> <p>HOT</p> </td> <td>HOT cruise number</td> <td> <p>#</p> </td> </tr> <tr> <td> <p>Date</p> </td> <td>Date of sampling and start of incubation (UTC -10)</td> <td> <p> </p> </td> </tr> <tr> <td> <p>Depth</p> </td> <td>Nominal depth of sampling and incubation </td> <td> <p>meters</p> </td> </tr> <tr> <td>GOP</td> <td>Gross oxygen production, average of 8 replicates</td> <td>mmol O<sub>2</sub> m<sup>-3</sup> d<sup>-1</sup></td> </tr> <tr> <td>GOP SE</td> <td>Gross oxygen production standard error </td> <td>mmol O<sub>2</sub> m<sup>-3</sup> d<sup>-1</sup></td> </tr> <tr> <td>CR</td> <td> <p>Dark community respiration, average of 8 replicates</p> </td> <td> <p>mmol O<sub>2</sub> m<sup>-3</sup> d<sup>-1</sup></p> </td> </tr> <tr> <td> <p>CR SE</p> </td> <td>Dark community respiration standard error</td> <td> <p>meters</p> </td> </tr> <tr> <td>NCP</td> <td>Net community production,average of 8 replicates </td> <td>mmol O<sub>2</sub> m<sup>-3</sup> d<sup>-1</sup></td> </tr> <tr> <td>NCP SE</td> <td>Net community production standard error </td> <td>mmol O<sub>2</sub> m<sup>-3</sup> d<sup>-1</sup></td> </tr> </tbody> </table> <p> </p>
Figure 3 in The first in situ collection of a mosasaurine from the marine Breien Member of the Hell Creek Formation in south-central North Dakota, USA
Figure 3. Right articular-prearticular complex, NDGS 2729. A. Dorsal view. B. Medial view. Specimen oriented anterior to the left. Abbreviations: ac, adhered concretion; gf, glenoid fossa; rp, retroarticular process; sas, articulation surface for the surangular.
Figure 2 in The first in situ collection of a mosasaurine from the marine Breien Member of the Hell Creek Formation in south-central North Dakota, USA
Figure 2. Stratigraphic description of the study site, NDGS L301. The original thickness of the Breien Member is not preserved at the site, with the upper prairie surface situated within the upper portion of the Breien Member. Burrows within the Breien Member are largely referable to Ophiomorpha sp., while those in the underlying "Undifferentiated Hell Creek Formation" are small (~3.0–4.0 mm thick) terrestrial burrows and root traces within an organic-rich paleosol.
Figure 1 in The first in situ collection of a mosasaurine from the marine Breien Member of the Hell Creek Formation in south-central North Dakota, USA
Figure 1. Geographic distribution of outcrops of the Breien Member of the Hell Creek Formation in south-central North Dakota. Surficial outcrops of the Hell Creek Formation shaded gray. Locations of measured sections shown by open circles, while published fossil localities are indicated with black diamonds. Study site is marked by a white star. Abbreviations: A, University of North Dakota paleontological locality number; Crowghost, Crowghost Cemetery Reference Section (Hoganson and Murphy); F, measured section from Frye (); FR, Fort Rice reference section; H, measured section from Hoganson and Murphy (); L, North Dakota Geological Survey (NDGS) paleontological locality number (Hoganson and Murphy); LM, measured section from Laird and Mitchell (); N, north; State, State Butte Reference Section (Hoganson and Murphy); Stumpf, Stumpf Composite Reference Section (Hoganson and Murphy).
Figure 7 in Epiplastral and geographic variation in Echmatemys, a geoemydid turtle from the Eocene of North America: A multi-tiered analysis of epiplastral shape complexity
Figure 7. Results of sliding semilandmark process from 3D data, and specimens warped along Principal Component 1 (PC1). A. Thin plate spline deformation grid showing transformation of Echmatemys callopyge mean type along PC1. B. 3D image of Echmatemys callopyge showing the positions of landmarks along the curve indicated in A, specimen no.UNMN.VP.27621. C. 3D image of Echmatemys uintensis showing the positions of landmarks along the curve indicated in D, UMNH.VP.27429. D. Thin plate spline deformation grid showing transformation of E. uintensis mean type along PC1.
Figure 5 in Epiplastral and geographic variation in Echmatemys, a geoemydid turtle from the Eocene of North America: A multi-tiered analysis of epiplastral shape complexity
Figure 5. Principal components plots from geometric morphometric analyses of 2D epiplastral shape data. A. Dorsal epiplastral shape: PC1 (49.3% variance) versus PC2 (16.7% variance). B. Ventral epiplastral shape: PC 1 (47.7% variance) versus PC2 (20.8%) variance.
Figure 4 in Epiplastral and geographic variation in Echmatemys, a geoemydid turtle from the Eocene of North America: A multi-tiered analysis of epiplastral shape complexity
Figure 4. Plot of Tooth-Midline versus Tooth-Lip (TM/TL) values for each specimen. The correlation between these two variables is significant (R2=0.403). Correlation coefficients do not differ significantly between any pair of taxa.
Figure 1 in Epiplastral and geographic variation in Echmatemys, a geoemydid turtle from the Eocene of North America: A multi-tiered analysis of epiplastral shape complexity
Figure 1. Morphological differences in dorsal epiplastral shape between Uintan Echmatemys species. A. Echmatemys callopyge (UMNH.VP.27220). B. Echmatemys uintensis (UMNH.VP.26558). The gular scale is indicated in grey.
Figure 2. A in Epiplastral and geographic variation in Echmatemys, a geoemydid turtle from the Eocene of North America: A multi-tiered analysis of epiplastral shape complexity
Figure 2. A. Standard linear measurements for quantifying the dimensions of the gular scale on the epiplastron of Echmatemys species depicted on UMNH.VP.27220. TM=tooth-midline: Distance between the epiplastral tooth and the anatomical midline. TL=tooth-lip: Distance between the epiplastral tooth and the caudal lip of the gular-humeral sulcus. B. Two-dimensional epiplastral landmarks and semilandmarks used in 2D geometric morphometric comparisons of this study: Ventral surface. Data points were digitized from digital photographs. C. Three-dimensional epiplastral landmarks and semilandmarks used in 3D geometric morphometric analyses in this study. All data points were obtained from 3D NextEngine laser scans. Scale bar=2 cm.
Fig. 8 in The history and nomenclatural significance of herbarium collections made by Alexander A. Tatarinow in North China and Mongolia in 1841-1850
Fig. 8. Herbarium labels used in the third set of Tatarinow's collections. Main text written by an unknown copyist, retouched or corrected in black ink by Tatarinow (A–F); identification added by P. Horaninow (C); curatorially identified (D, F) and annotated by V. Komarov (B); misattributed to P. Kirilov by V. Komarov (B, D, F); correctly attributed by V. Grubov (C). A, Prenanthes tatarinowii Maxim. (LE01024562); B, Plectranthus pekinensis Maxim. (LE01043049); C, Chionanthus chinensis Maxim. (LE01012808); D, Abelia biflora Turcz. (LE01043186); E, Leptodermis oblonga Bunge (LE01016141); F, Galium gracile Bunge (LE01016162).
Fig. 4 in The history and nomenclatural significance of herbarium collections made by Alexander A. Tatarinow in North China and Mongolia in 1841-1850
Fig. 4. Herbarium label forms printed by the Imperial Academy of Sciences in Saint Petersburg for Tatarinow's collections. A, Acquisition year 1851; B, Acquisition year 1856; taxonomic annotation and label data copied by C. Maximowicz. A, Spiraea kirilowii Regel (LE01015029); B, Pedicularis tatarinowii Maxim. (LE01034792).
Fig. 7 in The history and nomenclatural significance of herbarium collections made by Alexander A. Tatarinow in North China and Mongolia in 1841-1850
Fig. 7. Handwriting samples of Friedrich Körnicke from herbarium specimens at LE. A, C & E. Curatorial annotations; B & F, Identifications and curatorial annotations; D, Complete label. Note the shapes of P, k and H[er]b. Fischer. A, Acorus tatarinowii Schott (LE01182329); B, Banisteria fischeriana Regel & Körn. (LE00002995); C, Arisaema tatarinowii Schott (LE01205149); D, Banisteria fischeriana Regel & Körn. (LE00002997); E, Pinellia pedatisecta Schott (LE01169555); F, Paepalanthus lanuginosus (Bong.) Körn. (LE00001140).
Fig. 5 in The history and nomenclatural significance of herbarium collections made by Alexander A. Tatarinow in North China and Mongolia in 1841-1850
Fig. 5. Holotype specimen of Pedicularis tatarinowii Maxim., collected by A. Tatarinow in 1847 (LE01034792). Note (from top to bottom) an analytical drawing with the species name made by A. Maximowicz; an original label belonging to the second set of Tatarinow's collections; a revision label written by Tatarinow; a curatorial label with the species name and the label data translated into Latin by Maximo-wicz. A curatorial label on the right side belongs to V. Grubov.
Fig. 1 in The history and nomenclatural significance of herbarium collections made by Alexander A. Tatarinow in North China and Mongolia in 1841-1850
Fig. 1. Portrait of Alexander A. Tatarinow, presumably from 1880s. Original photograph deposited in the Penza State Museum of Local Studies.
Fig. 2 in The history and nomenclatural significance of herbarium collections made by Alexander A. Tatarinow in North China and Mongolia in 1841-1850
Fig. 2. Herbarium labels used in the first set of Tatarinow's collections. Complete text, including Chinese script (B) and additions (C), was written by A. Tatarinow. A, Oxytropis mandshurica Bunge (LE01024695); B, Pedicularis tatarinowii Maxim. (LE01034792); C, Orobanche mongolica Beck (LE01042560); D, Astragalus capillipes Bunge (LE01024141); E, Mitrosicyos racemosus Maxim. (LE01042541); F, Prenanthes tatarinowii Maxim. (LE01024560).
Fig. 3 in The history and nomenclatural significance of herbarium collections made by Alexander A. Tatarinow in North China and Mongolia in 1841-1850
Fig. 3. Contemporary identification labels used in Tatarinow's collections. A, B, E & F, First set; C, D & G, Second set. A, B, E & F, Revision labels written by A. Tatarinow; annotated by P. Horaninow (A, E); misattributed to Horaninow by V. Grubov (B). C, D & G, Identification labels written by Horaninow; label text added by Tatarinow (C). A, Mitrosicyos racemosus Maxim. (LE01042541); B, Astragalus capillipes Bunge (LE01024141); C & G, Prenanthes tatarinowii Maxim. (LE01024562); D, Chionanthus chinensis Maxim. (LE01012808); E, Oxytropis mandshurica Bunge (LE01024695); F, Pedicularis tatarinowii Maxim. (LE01034792).
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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OpenNeuro
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