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814 results for “Routing”
FIGURE 8 in Morphological and molecular data reveal the cryptic diversity among populations of Aegla paulensis (Decapoda, Anomura, Aeglidae), with descriptions of four new species and comments on dispersal routes and conservation status
FIGURE 8. Types of Aegla Leach, 1820 male sexual tubes. A, long and narrow (A. lancinhas Bond-Buckup & Buckup in Santos et al., 2015, MZUSP 34403). B, short and wide (A. leptochela Bond-Buckup & Buckup, 1994, MZUSP 34491).
FIGURE 1 in Morphological and molecular data reveal the cryptic diversity among populations of Aegla paulensis (Decapoda, Anomura, Aeglidae), with descriptions of four new species and comments on dispersal routes and conservation status
FIGURE 1. Distribution of the species of Aegla in four main hydrographic basins of southern Brazil: Rio Grande, Rio Tietê (Upper Paraná system), Rio Paraíba do Sul and Ribeira de Iguape. Indications L 1 through L 7 refer to the locations mentioned under “ sampling area ” in the Material & Methods section.
Data from : Metabolic footprint of Vero E6 cells highlights the key metabolic routes associated with SARS-CoV-2 infection and response to drug combinations
<p>This dataset contains representative 1D 1H NMR spectra and data used in the manuscript " Metabolic footprint of Vero E6 cells highlights the key metabolic routes associated with SARS-CoV-2 infection and response to drug combinations " . </p><p> </p><p>The present study used Nuclear Magnetic Resonance-based metabolic footprinting to characterize the secreted cellular metabolite levels (exometabolomes) of Vero E6 cells in response to SARS-CoV-2 infection and to two candidate drugs (Remdesivir, RDV and Azithromycin, AZI). </p><p> </p><p><strong>Supplementary File 1.zip = </strong>Representative 1D 1H NMR profiles of examined VE6 esometabolomes, </p><p> </p><p><strong>Supplementary File 2.xlsx</strong> = Average Mean ± Standard Deviations of NMR relative quantified data (integrals, a.u.) from examined VE6 esometabolomes. </p><p> </p><p><strong>Supplementary File 3.csv = </strong>p–values and associated False Discover Rate (FDR) derived from univariate ANOVA with Fischer's LDS post-hoc test comparisons carried out on NMR relative quantified data.</p><p> </p><p><strong>List of Supplementary Files derived from Metabolite Set Enrichment Analysis (MSEA) : </strong></p><p> </p><p><strong>Supplementary File 4.csv </strong>= Tabular Results from MSEA performed on VE6+ VE6- comparison.</p><p><strong>Supplementary File 5.csv </strong>= Tabular Results from MSEA performed on VE6+ RDV vs. VE6+ comparison.</p><p><strong>Supplementary File 6.csv </strong>= Tabular Results from MSEA performed on VE6+ AZI vs. VE6+ comparison.</p><p><strong>Supplementary File 7.csv</strong> = Tabular Results from MSEA performed on VE6+ R+A vs. VE6+ comparison.</p><p> </p>
A checklist of the spiders (Arachnida, Araneae) of the Garden Route National Park
<p>An annotated species list of spiders from the Garden Route National Park (GRNP) is provided. The checklist was compiled from data collected from the South African National Survey of Arachnida (SANSA) database. A total of 245 species from 52 families and 166 genera are presently protected in the park. The most species-rich families are the Thomisidae (34 spp.), Salticidae (28 spp.) and Araneidae (22 spp.), while 15 families are represented by singletons. The global distribution, endemicity and conservation status for each species is provided. A large percentage (83.2%) of the species have a wide distribution range and are of Least Concern while 17 species are Data Deficient and 10 species are of special concern. Seven species are known only from the Garden Route National</p>
Radiation hardness of ultrabroadband spintronic terahertz emitters: En-route to a space-qualified terahertz time-domain gas spectrometer
<p>Data for the publication "Radiation hardness of ultrabroadband spintronic terahertz emitters: En-route to a space-qualified terahertz time-domain gas spectrometer" accepted for publication in Applied Physics Letters. The following datasets are provided: time-domain raw data (dry vs ambient conditions) and corresponding Fourier amplitude spectra as well as the impedance of the spintronic THz emitter vs frequency, THz transmission Fourier amplitude spectra from a spintronic THz emitter propagating through a gas cell with CO2 and N2, CO2 absorption coefficient vs frequency from THz transmission measurements through the gas cell, electro-optic THz signals and corresponding Fourier amplitude spectra for gamma and proton irradiated spintronic THz emitters as well as THz amplitudes vs irradiation dose/proton fluence.</p>
CLDF dataset derived from Grollemund et al.'s "Bantu expansion shows habitat alters the route and pace of human dispersals" from 2015
<p>Cite the source of the dataset as:</p> <blockquote> <p>Grollemund, Rebecca, Branford, Simon, Bostoen, Koen, Meade, Andrew, Venditti, Chris, & Pagel, Mark (2015) Bantu expansion shows habitat alters the route and pace of human dispersals. Proc Natl Acad Sci USA. doi:10.1073/pnas.1503793112.</p> </blockquote>
Incidents of death and missing people on migratory routes around the world
<pre>Dataset with data on incidents of people dead or missing on international migratory routes in different regions, from the website https://missingmigrants.iom.int/, from the Missing Migrants Project of the International Organisation for Migration (IOM). </pre>
Maritime routes and vessel tracklet dataset for vessel-to-route association
<p>With an ever-increasing number of vessels at sea, the modelling, analysis and visualisation of maritime traffic are of paramount importance to support the monitoring tasks of maritime stakeholders. Sensors have been developed in this respect to track vessels and capture the maritime traffic at the global scale. The Automatic Identification System (AIS) is transmitting maritime positional and nominative information at highest frequency rate, making it a valuable source for maritime traffic modelling. From an original AIS dataset covering the area of Brest, France, we extracted a set of 17 maritime routes, connecting ports in this area. Two different representations for the routes are provided: (1) clusters of AIS contacts, and (2) route prototypes, representing the nominal trajectory of the vessels following the route. Additionally, a set of tracklets (built by five consecutive AIS contacts from the same vessel trajectory) has been extracted from the set of routes and the original dataset, and labelled either with the route name to which they belong or as off-route tracklets. This dataset provides thus some ground truth on the routes followed by vessels and is aimed at testing and validating vessel-to-route or track-to-route association algorithms.</p>
Ontario Lake-River Routing Product version 1.0
<p>Thank you for your interest in our lake-river routing product. Please go to this <a href="https://lake-river-routing-products-uwaterloo.hub.arcgis.com/">website </a>to download and learn more about the Routing product and BasinMaker. </p> <p>In your publication using the version v1.0 of the routing product, please cite the following paper:</p> <p>BasinMaker: a GIS toolbox for distributed watershed delineation of complex lake and river routing networks. Han, M., H. Shen, B. A. Tolson, J. R. Craig, J. Mai, S. Lin, N. Basu, F. Awol, submitted April 2021 to Environmental Modelling and Software.</p> <p>(But please also check BasinMaker website where you downloaded this for the most up to date citation)</p> <p>Note that version 1.0 of this product covered only Canada and used a different DEM and is described in the following paper:</p> <p>Han, M., J. Mai, B. A. Tolson, J. R. Craig, E. Gaborit, H. Liu, K. Lee, Subwatershed-based lake and river routing products for hydrologic and land surface models applied over Canada, Canadian Water Resources Journal, 45(3), doi.org/10.1080/07011784.2020.1772116.</p> <p> </p> <p>The lake-river routing product provides a routing structure (which here refers to both the topology of the stream network and the contributing areas to individual lakes and stream reaches), to correctly represent lakes and be easily customized based on various user requirements.</p> <p>BasinMaker, which is a GIS toolbox to delineate watersheds with lakes, was used to develop this routing product. In this routing product, each lake is represented by a lake catchment. A lake catchment is defined by the following rules:1) The extent of the lake catchment will fully cover the lake; 2) the outlet of the lake catchment is the same as the outlet of the lake; 3) each lake’s inlets are treated as a catchment outlet. In this way, both inflow and outflow of each lake can be explicitly simulated by hydrologic routing models.</p> <p>Support for BasinMaker and the Ontario lake-river routing product development came from the Ontario Ministry of Northern Development, Mines, Natural Resources and Forestry.</p>
Data from: Hidden in plain sight: migration routes of the elusive Anadyr bar-tailed godwit revealed by satellite tracking
<p><strong>Abstract</strong></p> <p>Satellite and GPS tracking technology continues to reveal new migration patterns of birds which enables comparative studies of migration strategies and distributional information useful in conservation. Bar-tailed godwits in the East Asian–Australasian Flyway <em>Limosa lapponica baueri </em>and <em>L. l. menzbieri</em> are known for their long non-stop flights, however these populations are in steep decline. A third subspecies in this flyway, <em>L. l. anadyrensis</em>, breeds in the Anadyr River basin, Chukotka, Russia, and is morphologically distinct from <em>menzbieri</em> and <em>baueri</em> based on comparison of museum specimens collected from breeding areas. However, the non-breeding distribution, migration route and population size of <em>anadyrensis </em>are entirely unknown. Among 24 female bar-tailed godwits tracked in 2015–2018 from northwest Australia, the main non-breeding area for <em>menzbieri</em>, two birds migrated further east than the rest to breed in the Anadyr River basin, i.e. they belonged to the <em>anadyrensis </em>subspecies. During pre-breeding migration, all birds staged in the Yellow Sea and then flew to the breeding grounds in the eastern Russian Arctic. After breeding, these two birds migrated southwestward to stage in Russia on the Kamchatka Peninsula and on Sakhalin Island en route to the Yellow Sea. This contrasts with the other 22 tracked godwits that followed the previously described route of <em>menzbieri</em>, i.e. they all migrated northwards to stage in the New Siberian Islands before turning south towards the Yellow Sea, and onwards to northwest Australia. Since the Kamchatka Peninsula was not used by any of the tracked <em>menzbieri</em> birds, the 4 500 godwits counted in the Khairusova–Belogolovaya estuary in western Kamchatka may well be <em>anadyrensis</em>. Comparing migration patterns across the three bar-tailed godwits subspecies, the migration strategy of <em>anadyrensis </em>lies between that of <em>menzbieri </em>and <em>baueri</em>. Future investigations combining migration tracks with genomic data could reveal how differences in migration routines are evolved and maintained.</p> <p> </p> <p><strong>Data set</strong></p> <p>Stopping sites and migration timing of satellite-tracked bar-tailed godwits in the East Asian-Australasian Flyway</p> <p>file name: Chan et al. 2022 BARG_Stops_Timing.xlsx</p> <p>The sheet 'stopping_sites' contains stopping sites of bar-tailed godwits tracked with solar Argos satellite transmitters, and their respective arrival and departure times at each site. The sheet 'timing' contains departure and arrival times at the non-breeding and breeding sites in 2017. The transmitters were deployed in Roebuck Bay and Eighty Mile Beach, Australia, and were operating on an 8 h on and 25 h off duty cycle. </p> <p> </p> <p>Measurements of satellite-tracked bar-tailed godwits in the East Asian-Australasian Flyway</p> <p>file name: Chan et al. 2022 BARG_measurements.csv</p> <p>The datafile contains bill, wing and tarsus lengths and sex of bar-tailed godwits tracked with solar Argos satellite transmitters. The birds were captured in Roebuck Bay and Eighty Mile Beach, Australia. </p> <p> </p> <p><strong>Journal Article</strong></p> <p>Chan, Y.-C., Tibbitts, T. L., Dorofeev, D., Hassell, C. J. and Piersma T. (2022) Hidden in plain sight: migration routes of the elusive Anadyr bar-tailed godwit revealed by satellite tracking. J Avian Biol e02988. <a href="https://doi.org/10.1111/jav.02920">https://doi.org/10.1111/jav.02988</a></p>
Initial relevant routes and geospatial objects for refugees and asylum seekers in MS
<p>Open geospatial dataset with an initial collection of routes, landmarks, and decision and confirmation points relevant for young refugees and asylum seekers arriving to Münster (MS), Germany. The information here collected were the results of participatory workshops done with young forced migrants in 2016.</p> <p>The information of the routes, landmarks (reference objects), points (origin, destination, decision, and confirmation points) and the relationship between points and reference objects is available in .JSON format. It has as an example, the images collected for one of the relevant routes (R2) identified by the group of young forced migrants. This route is the one from the main mall downtown (Arkaden) MS to the central train station. The pictures are available in .zip format.</p> <p> </p>
Source Location Privacy Aware Routing Protocols Selection Results
<p>This is the dataset used to generate the results for the journal paper " A Decision Theoretic Framework for Selecting Source Location Privacy Aware Routing Protocols in Wireless Sensor Networks" at Future Generation Computer Systems (FGCS) 2018.</p> <p> </p> <p> </p>
Data for a publication "The role of the preparation route on microstructure and mechanical properties of AlCoCrFeNi high entropy alloy"
<p>A dataset containing data for the published article "The role of the preparation route on microstructure and mechanical properties of AlCoCrFeNi high entropy alloy".</p> <p> </p> <p>For more details, please read the <strong>README Description of data and analysis.txt</strong> file.</p> <p> </p> <p> </p>
Рис. 3. Остров ЗавьяΛова, виΑ от п-ова Старицкого Fig. 3. Zavyalov island, a view from Staritsky Peninsula in Brown bear (Ursus arctos) of Zavyalov Island (Sea of Okhotsk): Abundance and possible migration routes
Рис. 3. Остров ЗавьяΛова, виΑ от п-ова Старицкого Fig. 3. Zavyalov island, a view from Staritsky Peninsula
Рис. 1. Αиния маршрута; цифры — места, гΑе быΛи отмечены особи бурого меΑвеΑя во время учетов с вертоΛета 22.05.2018. РезуΛьтаты учетов бурого меΑвеΑя на о. ЗавьяΛова с вертоΛета «Еврокоптер 120». 11:55 выΛет с нефтепирса г. МагаΑана, 12:14 поΑΛет к острову, 12:20 (1) отмечен первый моΛоΑой меΑвеΑь на террасе, 12:52 (2) отмечен оΑин взросΛый меΑвеΑь, 13:06 (3, 4) отмечены Αва взросΛых меΑвеΑя, 13:08 (5, 6, 7) отмечены три взросΛых меΑвеΑя, 13:18 (8) отмечен оΑин взросΛый меΑвеΑь. 13:56 переΛет в гороΑ МагаΑан Fig. 1. Route line; the figures indicate areas where brown bears were seen during the helicopter surveys on 22 May 2018. The results of the brown bear surveys on Zavyalov island from the Eurocopter 120 helicopter. 11:55 departure from the oil pier of Magadan, 12:14 hovering near the island, 12:20 (1) the first young bear identified on the terrace, 12:52 (2) one adult bear identified, 13:06 (3, 4) two adult bears identified, 13:08 (5, 6, 7) three adult bears identified, 13:18 (8) one adult bear identified, 13:56 Flight to Magadan in Brown bear (Ursus arctos) of Zavyalov Island (Sea of Okhotsk): Abundance and possible migration routes
Рис. 1. Αиния маршрута; цифры — места, гΑе быΛи отмечены особи бурого меΑвеΑя во время учетов с вертоΛета 22.05.2018. РезуΛьтаты учетов бурого меΑвеΑя на о. ЗавьяΛова с вертоΛета «Еврокоптер 120». 11:55 выΛет с нефтепирса г. МагаΑана, 12:14 поΑΛет к острову, 12:20 (1) отмечен первый моΛоΑой меΑвеΑь на террасе, 12:52 (2) отмечен оΑин взросΛый меΑвеΑь, 13:06 (3, 4) отмечены Αва взросΛых меΑвеΑя, 13:08 (5, 6, 7) отмечены три взросΛых меΑвеΑя, 13:18 (8) отмечен оΑин взросΛый меΑвеΑь. 13:56 переΛет в гороΑ МагаΑан Fig. 1. Route line; the figures indicate areas where brown bears were seen during the helicopter surveys on 22 May 2018. The results of the brown bear surveys on Zavyalov island from the Eurocopter 120 helicopter. 11:55 departure from the oil pier of Magadan, 12:14 hovering near the island, 12:20 (1) the first young bear identified on the terrace, 12:52 (2) one adult bear identified, 13:06 (3, 4) two adult bears identified, 13:08 (5, 6, 7) three adult bears identified, 13:18 (8) one adult bear identified, 13:56 Flight to Magadan
FIG. 1 in Sighting of Saccorhiza polyschides (Lightfoot) Batters (Phaeophyceae, Stramenopiles) in Algeria (Mediterranean Sea): an insight into range expansion routes
FIG. 1. — Mediterranean records of Saccorhiza polyschides (Lightfoot) Batters. The date is that of the sighting and, if unknown, that of the publication. TABLE 1. — Mediterranean records of Saccorhiza polyschides (Lightfoot) Batters. Records from the Alboran Sea, close to the Straits of Gibraltar, are not reported.
Data from: Ontogeny of migration destination, route and timing in a partially migratory bird
<p><strong>Abstract</strong></p> <ol> <li>In migratory animals, the developmental period from inexperienced juveniles to breeding adults could be a key life stage in shaping population migration patterns. Nevertheless, the development of migration routines in early life remains underexplored. While age-related changes in migration routes and timing have been described in obligate migrants, most investigations into the ontogeny of partial migrants only focused on age-dependency of migration as a binary tactic (migrant or resident), and variations in routes and timing among individuals classified as ‘migrants’ is rarely considered. </li> <li>To fill this gap, we study the ontogeny of migration destination, route and timing in a partially migratory red kite (<em>Milvus milvus</em>) population. Using an extensive GPS-tracking dataset (292 fledglings and 38 adults, with 1 – 5 migrations tracked per individual), we studied how 9 different migration characteristics changed with age and breeding status in migrant individuals, many of which become resident later in life.</li> <li>Individuals departed later from and arrived earlier at the breeding areas as they aged, resulting in a gradual prolongation of stay in the breeding area by two months from the first to the fifth migration. Individuals delayed southward migration in the year prior to territory acquirement, and they further delayed it after occupying a territory. Migration routes became more direct with age. Individuals were highly faithful to their wintering site. Migration distance shortened only slightly with age and was more similar among siblings than among unrelated individuals.</li> <li>The large gradual changes in northward and southward migrations suggest a high degree of plasticity in temporal characteristics during the developmental window. However, the high wintering site fidelity points towards large benefits of site familiarity, prompting spatial migratory plasticity to be expressed through a switch to residency. </li> <li>The contrasting patterns of trajectories of age-related changes between spatial and temporal migration characteristics might reflect different mechanisms underlying the expression of plasticity. Investigating such patterns among species along the entire spectrum of migration tactics would enable further understanding of the plastic responses exhibited by migratory species to rapid environmental changes.</li> </ol>
Combining Bayesian optimization and automation to simultaneously optimize reaction conditions and routes
<p>Yield and Conversion measurements for iodoalkylation reaction of four different terminal alkynes. The reaction conditions as well as the equivalent of the reactants and reagents for each of the three optimizers are listed in the corresponding JSON file. </p>
Fig. 2 in Molecular Identification, Fatty Acid Profile and Trace Elements in a Stranded Fin Whale in Sabah (Borneo, Malaysia): Implications on Migration Routes and Trophic Ecology of Southern Fin Whales.
Fig. 2. (a) The phylogenetic tree showing the stranded baleen whale (Baleen whale KP/Sabah/02082012) clustered together with the fin whale Balaenoptera physalus (U13103, Z18633 and X61145). (b) The phylogenetic analysis of the cytochrome b gene sequence indicating that the stranded fin whale (Baleen whale KP/Sabah/02082012) is closely related to the specimen of fin whales from the southern hemisphere with accession number KC572845, which represents Balaenoptera physalus quoi.
Fig. 1 in Molecular Identification, Fatty Acid Profile and Trace Elements in a Stranded Fin Whale in Sabah (Borneo, Malaysia): Implications on Migration Routes and Trophic Ecology of Southern Fin Whales.
Fig. 1. Stranding site (red-filled triangle) of the fin whale at the Sitompok River (Lat. 05°34'672"N; Long.115°39'710"E) near Kuala Penyu (KP), a coastal town overlooking the South China Sea on the western shores of Sabah (Borneo, Malaysia) (inset map). The approximate location of the sighting of possible fin whales reported by De Boer (2000) is marked with a blue-filled circle. The distribution ranges of rorquals species, including fin whales, in the Philippine waters reported by Slijper et al. (1964) and Acebes (2014) are marked with green-filled circles. The locations of fin whales' migration ranges in Australian waters according to Aulich et al. (2019) are shown using red-filled circles. The stranding site of the unconfirmed fin whale species at Pulau Sugi (Junge 1950) is indicated by a yellow-filled circle.
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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