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2,001 results for “Orders”
Enumeration of Williamson Sequences of Even Order
<p>These files contain an enumeration of all inequivalent Williamson sequences of even orders n < 65 as defined in the paper "A SAT+CAS Method for Enumerating Williamson Matrices of Even Order" by Bright, Kotsireas, and Ganesh. This paper has been accepted to appear at AAAI-18, the thirty-second AAAI conference on artificial intelligence.</p> <p>Every line in each file contains exactly one Williamson sequence, with spaces separating the members A, B, C, and D of the Williamson sequences. The sequence entries are encoded using the characters + for 1 and - for −1.</p>
Position in the laying order has sex-specific consequences for reproductive success in adult black-headed gulls
<p><span>Mothers who produce multiple offspring within one reproductive attempt often allocate resources differentially; some maternally-derived substances are preferentially allocated to last-produced offspring and others to first-produced offspring. The combined effect of these different allocation regimes on the overall fitness of offspring produced early or late in the sequence is not well understood, partly because production order is often coupled with birth order, making it difficult to separate effects of pre-natal maternal allocation from those of post-natal social environments. In addition, very little is known about the influence of laying order on fitness in later-life. In this study, we used a semi-natural captive colony of black-headed gulls to test whether an offspring's position in the laying order affected its early life survival and later life reproductive success, independent of its hatching order. Later-laid eggs were less likely to hatch, but among those that did, survival to adulthood was greater than that of first-laid eggs. In adulthood, the laying order of females did not affect their likelihood of breeding in the colony, but male offspring hatched from last-laid eggs were significantly less likely to gain a breeding position than earlier-laid males. In contrast, later-laid female parents hatched lower proportions of their clutches than first-laid females, but hatching success was unrelated to the laying order of male parents. Our results indicate that gull mothers induce complex and sex-specific effects on both the early survival of their offspring and on long-term reproductive success through laying order effects among eggs of the same breeding attempt.<strong> </strong></span></p>
Figure data to "Quantitative description of long-range order in the spin-1/2 XXZ antiferromagnet on the square lattice"
<p>This collection contains the data of the figures shown in the publication "Quantitative description of long-range order in the spin-1/2 XXZ antiferromagnet on the square lattice" as txt files.</p> <p>The CST datasets "Fig1_Gap_CST.txt", "Fig1_Energy_CST.txt" and "Fig3_CST.txt" are already published in https://doi.org/10.5281/zenodo.7528316 and included here for the sake of completeness.</p>
FIG. 2. — C in Homogeneity of photosynthetic features in canopy-forming macroalgae of the order Fucales from shallow and sheltered environments
FIG. 2. — C:N, C:P, N:P ratios in tissues for each of the studied species. Names are abbreviations from those in Figure 1.
FIG. 1. — A in Homogeneity of photosynthetic features in canopy-forming macroalgae of the order Fucales from shallow and sheltered environments
FIG. 1. — A, photosynthesis/PFD curves for the tested algae, error bars refer to SE; B, lineal fitting of the Photosynthesis/PFD data for the tested algae at the lineal part of the curve. Cystoseira compressa stands for Cystoseira compressa subsp. pustulata (Ercegovic) Verlaque and Cystoseira foeniculacea for Cystoseira foeniculacea f. tenuiramosa (Ercegovic) A.Gómez Garreta, M.C.Barceló, M.A.Ribera & J.Rull Lluch.
Figure 4 in A new order of fishes as hosts of blood flukes (Aporocotylidae); description of a new genus and three new species infecting squirrelfishes (Holocentriformes, Holocentridae) on the Great Barrier Reef
Figure 4. Relationships between species of Holocentricola and other members of the Aporocotylidae based on phylogenetic analysis of the 28S dataset. Bayesian inference posterior probabilities values are shown above the nodes and maximum likelihood bootstrap support shown below; values of <85 and <0.85 not shown. The scale-bar indicates expected number of substitutions per site.
Figure 3 in A new order of fishes as hosts of blood flukes (Aporocotylidae); description of a new genus and three new species infecting squirrelfishes (Holocentriformes, Holocentridae) on the Great Barrier Reef
Figure 3. Species of Holocentricola from Great Barrier Reef Holocentridae, terminal genitalia, dorsal views; spines illustrated are ventral. (A) Holocentricola rufus n. sp. ex Sargocentron rubrum from off Heron Island (paratype, QM G239440); (B) Holocentricola exilis n. sp. ex Neoniphon sammara from off Lizard Island (paratype, QM G239119); (C) Holocentricola coronatus n. sp. ex Sargocentron diadema from off Lizard Island (paratype, QM G239126). Abbreviations: CS, cirrus-sac; ER, egg reservoir; FGP, female genital pore; MGP, male genital pore; Od, oviduct; Oö, oötype; Ov, ovary; PP, pars prostatica; SV, seminal vesicle; Ut, uterus; VD, vas deferens; VitD, vitelline duct. Scale-bars: A–C, 100 µm.
Figure 2 in A new order of fishes as hosts of blood flukes (Aporocotylidae); description of a new genus and three new species infecting squirrelfishes (Holocentriformes, Holocentridae) on the Great Barrier Reef
Figure 2. Species of Holocentricola from Great Barrier Reef Holocentridae, whole worms, ventral views. (A) Holocentricola rufus n. sp. ex Sargocentron rubrum from off Heron Island (holotype, QM G239429); (B) Holocentricola exilis n. sp. ex Neoniphon sammara from off Lizard Island (paratype, QM G239111); (C) Holocentricola coronatus n. sp. ex Sargocentron diadema from off Lizard Island (holotype, QM G239125). Scale-bars: A–C, 200 µm.
Forest microclimate data from 2nd order sites
<div> <h1>Description</h1> <p>Microclimate records collected from SAFE Project 2nd order sitesfrom 2013-2019</p> <h1>Projects</h1> <p> This dataset was collected as part of the following projects: </p><ul> <li><a href="https://safeproject.net/projects/project_view/111">https://safeproject.net/projects/project_view/111</a> </li> </ul> <p></p> <h1>Files</h1> <p>This dataset consists of 3 files: Hardwick_microclimate_2ndOrder.xlsx, Microclimate1319.csv, Microclimate1319.Rdata</p> <h2>Hardwick_microclimate_2ndOrder.xlsx</h2> <p>This file only contains dataset metadata.</p> <h2>Microclimate1319.csv</h2> <p>CSV file containing microclimate data </p> <p>This file contains 1 data tables:</p> <h3>Forest microclimate data from 2nd order sites</h3> <ul> <li>Worksheet: Data</li> <li>Description: Microclimate records collected from SAFE Project 2nd order sitesfrom 2013-2019</li> <li>Number of fields: 7</li> <li>Number of data rows: Unavailable (table metadata description only).</li> <ul> <li>Plot: Location of record (type: location)</li> <li>time: Date and time of record (type: datetime)</li> <li>Temp: Air temperature 1 m above ground (type: numeric)</li> <li>RH: Relative humidity. (type: numeric)</li> <li>DewTemp: Dewpoint temperature. (type: numeric)</li> <li>LoggerType: Make of datalogger that was used (Lascar or iButton) (type: id)</li> <li>LoggerID: Unique reference number for the datalogger (type: id)</li> </ul> </ul> <h2>Microclimate1319.Rdata</h2> <p>RData file containing object 'microclimate' that stores the data</p> <h1>Extents</h1> <ul> <li>Date range: 2013-05-08 to 2019-12-24</li> <li>Latitudinal extent: 4.632° to 4.771°</li> <li>Longitudinal extent: 116.948° to 117.703°</li> </ul> </div>
Fig. 3 in A report on 24 unrecorded bacterial species of Korea isolated in 2016, belonging to the orders Rhizobiales and Sphingomonadales in the class Alphaproteobacteria
Fig. 3. Neighbor-joining phylogenetic tree based on 16S rRNA gene sequences showing the relationship between the strains isolated in this study and their relatives in the Sphingomonadales of the Alphaproteobacteria. Bootstrap values (expressed as percentages of 1000 replications) over 70% are shown at nodes for neighbour-joining, maximum parsimony, and maximum likelihood methods, respectively. Filled circles and open circles indicate that the corresponding nodes were recovered by all treeing methods and by two treeing methods, respectively. Bootstrap values (>70%) are shown at nodes. Bar, 0.02 substitutions per nucleotide position.
Fig. 1 in A report on 24 unrecorded bacterial species of Korea isolated in 2016, belonging to the orders Rhizobiales and Sphingomonadales in the class Alphaproteobacteria
Fig. 1. Transmission electron micrographs of the strains isolated in this study. Strains: 1, HMF4680; 2, Gsoil 1041; 3, YC4-26; 4, 16_S3_ F7; 5, HMF4666; 6, SG2-5; 7, Gsoil 531; 8, KH7a; 9, Gsoil 3034-1; 10, 16_S4_T9; 11, CAU 1113; 12, IMCC25650; 13, IMCC25649; 14, JMS-19; 15, HMF8222; 16, HMF6028; 17, MMS16-CNU530; 18, HMF6507; 19, CAU 1116; 20, EMML2331-1; 21, Gsoil 130; 22, Gsoil 187; 23, CAU 1064; 24, IMCC25648.
Dataset for "Finding order in chaos: Quantitative predictors of chaos terrain morphology on Europa"
<p>Dataset S1 contains two shapefiles containing the chaos borders (ChaosBordersShapefiles.zip) and each block mapped (AllBlocksShapefiles.zip), and a text file that contains the total area (km<sup>2</sup>) of each mapped chaos terrain and the area (km<sup>2</sup>) of every block we mapped within each chaos terrain in the manuscript "Finding order in chaos: Quantitative predictors of chaos terrain morphology on Europa".</p>
FIGURE 3 in Revised Evolutionary And Taxonomic Synthesis For Parrots (Order: Psittaciformes) Guided By Phylogenomic Analysis
FIGURE 3. Species-level topology of Psittacinae. Support values come from the maximum likelihood tree. Nodes have ultrafast bootstrap values of ≥95% otherwise noted.
FIGURE 8 in Revised Evolutionary And Taxonomic Synthesis For Parrots (Order: Psittaciformes) Guided By Phylogenomic Analysis
FIGURE 8. Photographs (not to scale) of Calyptomena hosii (left photo: Dubi Shapiro) a suboscine passerine of Borneo (Brunei, Indonesia) and Triclaria malachitacea (right photo: Marcos Eugênio) of southeastern Brazil showing presumably convergent evolution in ventral coloring. See text for discussion. Photographs reproduced with permission from the photographers.
FIGURE 16 in Revised Evolutionary And Taxonomic Synthesis For Parrots (Order: Psittaciformes) Guided By Phylogenomic Analysis
FIGURE 16. Dorsal view of specimens of Glossopsitta concinna from the Australian National Wildlife Collection (ANWC) showing variation within and between sexes and within and between mainland southeastern Australia versus Tasmania. Note the bluer coronal color in mainland males. Registration numbers from the bird collection at ANWC are shown. Photograph: Gordon Gullock.
Fig. 5. Phylogenetic relationships between jellyfishes within the order Semaeostomeae inferred from nearly complete 18S in Comprehensive Analysis of the Jellyfish (Goette, 1886) (Semaeostomeae: Pelagiidae) with Description of the Complete rDNA Sequence.
Fig. 5. Phylogenetic relationships between jellyfishes within the order Semaeostomeae inferred from nearly complete 18S rDNA (A) and partial 28S rDNA sequences (B) with maximum-likelihood (ML) algorithms. ML analyses of 18S and 28S were used as the nucleotide substitution model of GTR+G. Two hydrozoans (Hydractinia echinata and Podocoryne carnea for 18S rDNA; Astrohydra japonica and Melicertissa sp. for 28S) were included as the outgroups. Additional Bayesian analysis generated similar topology of the tree compared with the ML tree. Posterior probabilities (PP) from the analyses were incorporated into the ML tree to support the strength of each branch. The first and second numbers at the nodes display bootstrap proportions (BP) (> 50%) in ML and PP (> 0.50) in Bayesian, respectively. Branch lengths are proportional to the scale given. *Represents controversial species names, because they were suspected as different species by Bayha et al. (2017).
Fig. 3. A Neighbor-joining phylogenetic tree reconstructed from a in Isolation and characterization of two unrecorded yeast species in the order Filobasidiales
Fig. 3. A Neighbor-joining phylogenetic tree reconstructed from a comparative analysis of 26S rRNA gene sequences showing the rela- tionships of strain PG1-1-10C with closely related species. Bootstrap values (>70%) based on neighbor-joining methods are shown at the branch nodes. Bar, 0.01 substitutions per nucleotide position.
Fig. 2. A Neighbor-joining phylogenetic tree reconstructed from a in Isolation and characterization of two unrecorded yeast species in the order Filobasidiales
Fig. 2. A Neighbor-joining phylogenetic tree reconstructed from a comparative analysis of 26S rRNA gene sequences showing the relation- ships of strains GW1-3 with closely related species. Bootstrap values (>70%) based on neighbor-joining methods are shown at the branch nodes. Bar, 0.01 substitutions per nucleotide position.
Figure 4. After merging, overview is more transparent. Tens of persons were merged together into clusters in order to clarify the visualization. Firms and persons are recognized based on their icons.-Browsing Semantic Data in Slovakia
<p>The usefulness of such visualization has its key points regarding connections. Thanks to SBR browsing module, we were able to get 22 firm records for “Váhostav” query. Between any 2 companies, connections may be (and often are) not bidirectional, so, in order to navigate through connections, we have refined all 22 records. Although, even being filtered, graph is still complex. And it is possible to further navigate and search for outgoing connections, for example firm “MERLIN TRADE, a.s.” on Fig.4 contains item on “Ján Kato”, which is already included in our graph and connected to “VÁHOSTAV&SK&DEVELOPEMENT” on bottom left side and “VÁHOSTAV&SK, a.s.” in the center. Edge coloring and drawing is helpful with overlapped edges. For methods of visualization, including coloring, we refer to studies of H. Omote and K. Sugiyama (2006), and I. Herman, G. Melanon, and M. S. Marshall (2000) or our study on graph clutter filtering and connectivity distance (Mojzis & Laclavik, 2014).</p>
BRAIN Journal-The Presence and Activity on Facebook of the Informative Travel Organizations in Romania-Figure 1. Selected Romanian counties in order to strengthen the target group of tourism organizations with informative role
<p>In this regard, we analysed the current state of presence and communication on Facebook for<br> 109 informative tourism entities located in 25 Romanian counties, selected on the basis of tourist<br> traffic indicators for the period between 2007 and 2013. The structure of the 109 organizations<br> analysed is: 43 tourist information centers (39.45%), 44 entities with the name of the association for<br> tourism promotion, ecotourism promotion, mountaineering promotion etc. (40.36%), 18 tourism<br> clubs (16.51%) and 4 tourist information points/offices (3.67%)</p>
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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)
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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.