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2,516 results for “Seri”
Raw time series of GNSS sites used in the manuscript 'South China plate motion modified by 2008 Mw7.9 great Wenchuan earthquake'
<p>The *.pre.*.neu files are raw position time series before the Wenchuan earthquake (from July 2001 to December 2004) and the *.aft.*.neu files are the raw position time series after the Wenchuan earthquake (from July 2014 to December 2017). The file 'breaks' contains the epochs of breaks due to equipment changes or that are identified visually.</p>
3D ED tilt series of PPEA
<p>Data recorded with EPU-D Glacios TEM (Thermofisher) operating at 200 kV in continuous diffraction mode. The tilt sequence starts at -60°, tilt increment 1°, rotation speed 1° per second. Pixel size within the diffraction frames is 0.00098 Å-1, electron beam dimeter on the sample 1.5 µm (nano-electron diffraction mode). Electron dose rate during data collection was 6.016e/nm<sup>2</sup>s, liquid nitrogen temperature was used.</p> <p>2022-06-16-151539_sh_176.3457.mrc - the same dataset, centered and rotated to make the tilt axis run horizontally.</p> <p>2022-06-16-151539_sh_176.3457_SMV.7z, tar - the same dataset in SMV format.</p> <p>MRC2SMV_BS.exe - MRC to SMV converter, written in MatLab, compiled with mcc. Works with the current version (20140?) of EPU-D MRC files. MRC2SMV_BS.exe requires MATLAB Runtime R2018b (9.5), which can be downloaded free of charge from https://de.mathworks.com/products/compiler/matlab-runtime.html</p> <p> </p>
Shape coordinates and centroid size for adults and ontogenetic series analyzed in predictable complexity of evolutionary allometry
<p>Allometry has been a paradigm of constraints, including intrinsic constraints on the evolvability of allometry, as a source of developmental and genetic constraints on the evolution of form, and of functional constraints, maintaining functional equivalence as body size evolves. Yet, allometry may be the simplest case of varied constraints, and of morphological integration, even though allometry itself is not simple. Evolutionary allometry may be especially complex because it depends not only on the developmental origins of allometry and determinants of allometric variation but also on the evolutionary dynamics of size and shape. It should also depend on the ecological opportunity for size-dependent ecomorphological specialization. We predict that lineages that converge in those would exhibit similar evolutionary allometries but otherwise, evolutionary allometries would be heterogeneous. Countering this expectation are familiar craniofacial evolutionary allometries, often ascribed to developmental bias. To test both those hypotheses, we compare evolutionary allometries of mandibles across lineages of squirrels and evolutionary to growth allometries. As expected, lineages that converge on size-dependent specializations exhibit similar evolutionary allometries, but otherwise, their allometries are no more similar than expected by chance. Growth allometries of squirrels (and a cricetid rodent) slightly resemble the evolutionary allometry of one lineage, but growth allometries of species from other lineages are orthogonal to their own lineages' evolutionary allometry. We would expect that craniofacial allometries that are not brain-driven would, like mandibular evolutionary allometries, be predictable only from size-dependent ecological specializations.</p>
Public Profile Settings (TRIPLE Video Tutorial Series)
<p>In this tutorial series, researcher Agnieszka Szulińska and Research Infrastructure Coordinator Edward Gray discuss gotriple.eu. This episode explores the opportunities GoTriple offers for the creation of a public profile.</p> <p>Video recorded and edited by Fabian Fess.</p>
Sub-analysis results of pre- and post-intervention surveys of respondents who completed the educational lecture series
<p>Sub-analysis results of pre- and post-intervention surveys of respondents who completed the educational lecture series.</p>
Mean wind and stability time series at FINO1 between June and July 2015 (from OBLEX-F1)
<p>Data collected from a sonic anemometer mounted at 15m above the mean sea level at the geographical location of FINO1 offshore met-mast. Time series cover yeardays between 160 and 210, 2015.</p> <p>% % Datasets are as follows:</p> <p>% % time15: mean time at each 30-min burst of 15m sonic data.</p> <p>% % umean15: mean wind speed at 15m height from average of each sonic 30-min segment at 15m sonic.</p> <p>% % UU10: wind at 10m heigh from umean15 using logarithmic wind profile.</p> <p>% % ti_ref: reference time - first of January 2015.</p> <p>% % wdir: wind direction at 15m measured from high freq. sonic data.</p> <p>% % wa: wave age data estimated from sonic data and wave phase speed (see OBLEX-F1 data).</p> <p>% % L15: Moninnon-Obukhov length scale measured by 25Hz sonic data at 15m height.</p> <p>% %</p> <p>% % Mostafa Bakhoday Paskyabi, 10 Dec. 2022</p> <p>% % Mostafa.Bakhoday-Paskyabi@uib.no</p> <p> </p> <p> </p>
FIGURE 2. Pleurothallis mark-wilsonii J.S in Pleurothallis mark-wilsonii a new species from the subsection Acroniae series Amphigyae from the Western Andes of Colombia
FIGURE 2. Pleurothallis mark-wilsonii J.S.Moreno, Gal-Tar & Sierra-Ariza. A. Habit. B. Flower. C. Dissected perianth. D. Column and lip, lateral view and longitudinal section of the column. E. front and side view of lip. F. Column, ventral and side view. Anther cap and pollinia. LCDP by J.S. Moreno based on the holotype.
FIGURE 1. Pleurothallis mark-wilsonii J.S in Pleurothallis mark-wilsonii a new species from the subsection Acroniae series Amphigyae from the Western Andes of Colombia
FIGURE 1. Pleurothallis mark-wilsonii J.S.Moreno, Gal-Tar & Sierra-Ariza. A. Habit. B. Flower. C. Dissected perianth. D. Column and lip, lateral view and longitudinal section of the column. E. front and side view of lip. F. Column, ventral and side view. Drawing by J.S. Moreno based on the holotype.
FIGURE 10. Neocarus paraplatensis n in Redescription of Neocarus platensis Silvestri, 1905 (Acari: Opilioacaridae) and a new species from the syntype series
FIGURE 10. Neocarus paraplatensis n. sp. Male. (A) Palp ventral and dorsal view (tarsus omitted), (B) details of palp tarsus.
FIGURE 9. Neocarus paraplatensis n in Redescription of Neocarus platensis Silvestri, 1905 (Acari: Opilioacaridae) and a new species from the syntype series
FIGURE 9. Neocarus paraplatensis n. sp. Male. (A) Dorsal shield, (B) lateral view of chelicera, (C) sternitogenital area, (D) ventral view of subcapitulum, (E) anal region. Abbreviations: oc = ocelli; sv = sternal verrucae, pgc = pregenital capsule, pg = pregenital area; g = genital area.
FIGURE 3 in Redescription of Neocarus platensis Silvestri, 1905 (Acari: Opilioacaridae) and a new species from the syntype series
FIGURE 3. Neocarus platensis. (A) Female dorsal shield, (B) female sternitogenital region and ovipositor, (C) male sternitogenital region; anal regions, (D) female, (E) male. Abbreviations: oc = ocelli; sv = sternal verrucae, pgc = pregenital capsule, pg = pregenital area; g = genital area; eug = eugenital setae; ov = ovipositor; ogc = orifice of cheliceral gland.
FIGURE 6. Neocarus paraplatensis n in Redescription of Neocarus platensis Silvestri, 1905 (Acari: Opilioacaridae) and a new species from the syntype series
FIGURE 6. Neocarus paraplatensis n. sp. Female (A) dorsal shield, (B) anal region, (C) dissected sternitogenital region, (D) dissected sternitogenital region with ovipositor. Abbreviations: oc = ocelli; sv = sternal verrucae, pgc = pregenital capsule, pg = pregenital area; g = genital area; eug = eugenital setae; ov = ovipositor; ly = lyrifissure.
FIGURE 1 in Redescription of Neocarus platensis Silvestri, 1905 (Acari: Opilioacaridae) and a new species from the syntype series
FIGURE 1. Collection sites of N. platensis, N. paraplatensis n. sp., N. entrerios, N. misiones and undescribed Neocarus species.
FIGURE 2 in Redescription of Neocarus platensis Silvestri, 1905 (Acari: Opilioacaridae) and a new species from the syntype series
FIGURE 2. (A) Previous condition of the Neocarus platensis syntypes slides before remounting; (B) Neocarus platensis syntype slide manual process of Canadian Balsam removal.
FIGURE 8. Neocarus paraplatensis n in Redescription of Neocarus platensis Silvestri, 1905 (Acari: Opilioacaridae) and a new species from the syntype series
FIGURE 8. Neocarus paraplatensis n. sp. Female (A) Phase contrast microscopy of sternitogenital region, (B) detail of ovipositor projections; differential interference contrast of (C) ovipositor, (D) palp tarsus. Arrows: ovipositor projections.
FIGURE 7. Neocarus paraplatensis n in Redescription of Neocarus platensis Silvestri, 1905 (Acari: Opilioacaridae) and a new species from the syntype series
FIGURE 7. Neocarus paraplatensis n. sp. Female. (A) Ventral view of subcapitulum, (B) dorsal and ventral view of palp tarsus, (C) dorsal and ventral view of palp (tarsus omitted).
FIGURE 5 in Redescription of Neocarus platensis Silvestri, 1905 (Acari: Opilioacaridae) and a new species from the syntype series
FIGURE 5. Neocarus platensis. Palp (dorsal and ventral view). Female, (A) trochanter to tibia, (B) detail of the tarsus; male, (C) genu and tibia, (D) detail of the tarsus.
Aphanomerus americanus Brues, syntype series
<p><em>Aphanomerus americanus</em> Brues, syntype series, </p> <p>©Milwaukee Public Museum</p> <p> </p>
Shallow Slow Slip Events Identified Offshore the Osa Peninsula in Southern Costa Rica from GNSS Time Series
<p>Using new continuous GNSS time series from the region, we identify 5 distinct shallow SSEs that occurred immediately offshore and beneath the Osa peninsula: an event detected by one site in 2013, and two events occurring in close succession in both 2018 and 2022 detected by multiple stations, indicating a preliminary recurrence interval of ~4-5 years. While SSEs have been observed to the north at Nicoya, this is their first documentation in southern Costa Rica. Modeled slip distributions of the 2018 and 2022 events indicate that they ruptured the same or overlapping patches of the plate interface, nearly at the trench, updip of historic earthquakes including the 1983 Mw 7.4 Osa event. Immediately offshore, the estimated cumulative slip from the 2018 and 2022 events is sufficient to close the slip deficit from tectonic loading over the recurrence interval, likely influencing the magnitude and spatial slip distribution of future large ruptures.</p>
FIGURE 51 in First cladistic analysis of Toxotarsinae (Diptera: Calliphoridae), with insights on the evolution of the group and on the transformation series of some historically controversial characters
FIGURE 51. Cladistic analysis of Toxotarsinae. Single most parsimonious tree recovered with TNT in the equal weighting analysis, with characters and character states mapped to each branch. Black dots represent non-ambiguous synapomorphies and white dots represent non-ambiguous homoplasies, with character numbers given above the branches and state numbers for the respective characters given below the branches.
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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.