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Supplementary material 7 from: Yi P, Yu P, Liu J, Xu H, Liu X (2018) A DNA barcode reference library of Neuroptera (Insecta, Neuropterida) from Beijing. ZooKeys 807: 127-147. https://doi.org/10.3897/zookeys.807.29430
Table S1. Intraspecific and interspecific divergence of Coniopterygidae based on COI barcode sequences (%) : Explanation note: The range of interspecific distance = means interspecific distance ± standard error. N/A indicates intraspecific distance not available because only one specimen was sequenced.
Supplementary material 3 from: Yi P, Yu P, Liu J, Xu H, Liu X (2018) A DNA barcode reference library of Neuroptera (Insecta, Neuropterida) from Beijing. ZooKeys 807: 127-147. https://doi.org/10.3897/zookeys.807.29430
Figure S3. Photographs of male genitalia of species of Hemerobiidae newly recorded from Beijing : Explanation note: A. Drepanepteryxalgida (Erichson, 1851); B. Hemerobiusbispinus Banks, 1940; C. Hemerobiusexoterus Navás, 1936; D. Hemerobiushumulinus Linnaeus, 1758; E. Hemerobiusjaponicus Nakahara, 1915; F. Hemerobiusmarginatus (Stephens, 1836); G. Hemerobiussubtriangulus Yang, 1987; H. Sympherobiusmanchuricus Nakahara, 1960. Scale bar: 0.5 mm.
Supplementary material 10 from: Yi P, Yu P, Liu J, Xu H, Liu X (2018) A DNA barcode reference library of Neuroptera (Insecta, Neuropterida) from Beijing. ZooKeys 807: 127-147. https://doi.org/10.3897/zookeys.807.29430
Table S4. Intraspecific and interspecific divergence of Myrmeleontidae and Ascalaphidae based on COI barcode sequences (%) : Explanation note: The range of interspecific distance = mean interspecific distance ± standard error. N/A indicates intraspecific distance not available because only one specimen was sequenced.
Supplementary material 1 from: Yi P, Yu P, Liu J, Xu H, Liu X (2018) A DNA barcode reference library of Neuroptera (Insecta, Neuropterida) from Beijing. ZooKeys 807: 127-147. https://doi.org/10.3897/zookeys.807.29430
Figure S1. Photographs of male genitalia of species of Coniopterygidae newly recorded from Beijing : Explanation note: A. Conwentziasinica Yang, 1974; B. Semidalisbicornis Liu & Yang, 1993. Scale bar 0.5 mm.
Supplementary material 2 from: Yi P, Yu P, Liu J, Xu H, Liu X (2018) A DNA barcode reference library of Neuroptera (Insecta, Neuropterida) from Beijing. ZooKeys 807: 127-147. https://doi.org/10.3897/zookeys.807.29430
Figure S2. Photographs of male genitalia of species of Chrysopidae newly recorded from Beijing : Explanation note: A. Nothochrysasinica Yang, 1986; B. Chrysopaintima McLachlan, 1893; C. Chrysoperlafurcifera (Okamoto, 1914); D. Chrysopidiaciliata (Wesmael, 1841); E. Pseudomalladacognatellus (Okamoto, 1914); F. Pseudomalladaqinlingensis (Yang & Yang, 1989); G. Ninetagrandis Navás, 1915. Scale bar: 0.5 mm.
Normalization references for LCIA methods based on ecoinvent
<p>ecoinvent version 3.5</p> <p>see the corresponding article:</p> <p>Consistent normalization approach for Life Cycle Assessment based on inventory databases</p> <p><a href="https://doi.org/10.1016/j.scitotenv.2019.134583">https://doi.org/10.1016/j.scitotenv.2019.134583</a></p>
Survival of the self: Examinations of the role of self-reference in adaptive memory - DATASET
<p>Free recall data for</p> <p>Survival of the self: </p> <p>Examinations of the role of self-reference in adaptive memory</p>
Database on 16 reinforced concrete walls with lap splices and 8 reference units with continuous reinforcement (V2 models included)
<p>Recent post-earthquake missions have shown that both old and code-compliant reinforced concrete wall buildings can experience critical damage due to lap splices, which led to a recent surge in experimental tests of walls with such constructional detail. Most of the 16 walls with lap splices described in the literature thus far were carried out in the last five years. A database with these wall tests, plus 8 reference unit walls with continuous reinforcement, is herein provided alongside with the shell element models developed in Vector2 to simulate their inelastic F-D response</p> <p><strong>If the experimental data or the models are used, please cite:</strong></p> <p>- J.P. Almeida, O. Prodan, D. Tarquini, K. Beyer, 2017. "<em>Influence of lap-splices on the cyclic inelastic response of<br> reinforced concrete walls. I: Database assembly, recent experimental data, and findings for model development</em>", ASCE<br> Journal of Structural Engineering 143 (12), DOI: 10.1061/(ASCE)ST.1943-541X.0001853.</p> <p>- D. Tarquini, J.P. Almeida, O. K. Beyer, 2017. <em>"Influence of lap-splices on the cyclic inelastic response of reinforced<br> concrete walls. II: Shell element simulation and equivalent uniaxial model</em>", ASCE Journal of Structural Engineering 143<br> (12), DOI: 10.1061/(ASCE)ST.1943-541X.0001859.</p>
Reference data for MITOS
<p>Reference data for MITOS. Contains</p> <p>- fasta databases for the BLAST searches (RefSeq release 39)</p> <p>- automatically covariance models for ncRNA searches (for tRNAs the models are taken from MiTFi http://dx.doi.org/10.1093/nar/gkv746)</p> <p>As described in http://dx.doi.org/10.1016/j.ympev.2012.08.023</p>
Plasticity in Collective Decision-Making for Robots: Creating Global Reference Frames, Detecting Dynamic Environments, and Preventing Lock-ins
<p>Swarm robots operate as autonomous agents and a swarm as a whole gets autonomous by its capability of collective decision-making.<br> Despite intensive research on models of<br> collective decision-making, the implementation in multi-robot systems is still challenging.<br> Here, we advance the state of the art by introducing more plasticity to the decision-making process and by increasing the task difficulty.<br> Most studies on large-scale multi-robot decision-making are limited to one instance of an iterated exploration-dissemination phase followed by successful and permanent convergence.<br> We investigate a dynamic environment that requires constant collective monitoring of option qualities.<br> Once a significant change in qualities is detected by the swarm, it has to collectively reconsider its previous decision accordingly.<br> This is only possible by preventing lock-ins, a global consensus state of no return.<br> In addition, we introduce a task of increased difficulty as the robots must locate themselves to assess the quality of an option.<br> Using local communication, swarm robots propagate hop-count information throughout the swarm to form a global reference frame.<br> We successfully validate our implementation in many swarm robot experiments concerning robustness to disruptions of the reference frame, scalability, and adaptivity to a dynamic environment.</p>
Reference annotations for the eQTL Catalogue
<p>Reference annotations for the eQTL Catalogue</p>
text-fig. 57. Diagrams showing the relations between age rank and clade rank and the SRC for pectinate components of the cladogram figured in Text-figure 55 and the total cladogram. Names of the diagrams refer to the terminal taxa to which the pectinate components lead. in The interrelationships and evolution of basal theropod dinosaurs
text-fig. 57. Diagrams showing the relations between age rank and clade rank and the SRC for pectinate components of the cladogram figured in Text-figure 55 and the total cladogram. Names of the diagrams refer to the terminal taxa to which the pectinate components lead.
text-fig. 16. Ventral view of the braincase, showing different states for characters 56 and 57. a, basal ornithischian Lesothosaurus diagnostics; based on Sereno (1991b). B, Syntarsus rhodesiensis based on QG 195; the postorbital processes of the laterosphenoid are broken in this specimen of Syntarsus; their attachments are placed above and slightly posterior to the trigeminal foramen. Abbreviations: boc, basioccipital; bpt, basipterygoid process; bsp, basisphenoid; bspr, basisphenoid recess; bt, basal tuber; fo, fenestra ovalis; Is, laterosphenoid; oc, occipital condyle; op, opisthotic; pop, paroccipital process; popls, postorbital process of the laterosphenoid; psp, parasphenoid; Roman numbers refer to the foramina for the exits of cranial nerves. Scale bars represent 10 mm. in The interrelationships and evolution of basal theropod dinosaurs
text-fig. 16. Ventral view of the braincase, showing different states for characters 56 and 57. a, basal ornithischian Lesothosaurus diagnostics; based on Sereno (1991b). B, Syntarsus rhodesiensis based on QG 195; the postorbital processes of the laterosphenoid are broken in this specimen of Syntarsus; their attachments are placed above and slightly posterior to the trigeminal foramen. Abbreviations: boc, basioccipital; bpt, basipterygoid process; bsp, basisphenoid; bspr, basisphenoid recess; bt, basal tuber; fo, fenestra ovalis; Is, laterosphenoid; oc, occipital condyle; op, opisthotic; pop, paroccipital process; popls, postorbital process of the laterosphenoid; psp, parasphenoid; Roman numbers refer to the foramina for the exits of cranial nerves. Scale bars represent 10 mm.
text-fig. 7. Outgroup (a) and theropod (b-g) skull reconstructions in lateral view showing different character states of several cranial characters. For sources of reconstructions and identifications of the bones see Text-figures 4-6. a, Euparkeria capensis. B, Syntarsus rhodesiensis. c, Ceratosaurus sp. D, Allosaurus fragilis. E, Gorgosaurus libratus. F, Velociraptor mongoliensis. Character state indications in this and all following illustrations are as follows: numbers refer to characters discussed in the text; the first number indicates the number of the character, the second the character state. Scale bars represent 10 mm (a-b), 50 mm (f-g) and 100 mm (c-e). in The interrelationships and evolution of basal theropod dinosaurs
text-fig. 7. Outgroup (a) and theropod (b-g) skull reconstructions in lateral view showing different character states of several cranial characters. For sources of reconstructions and identifications of the bones see Text-figures 4-6. a, Euparkeria capensis. B, Syntarsus rhodesiensis. c, Ceratosaurus sp. D, Allosaurus fragilis. E, Gorgosaurus libratus. F, Velociraptor mongoliensis. Character state indications in this and all following illustrations are as follows: numbers refer to characters discussed in the text; the first number indicates the number of the character, the second the character state. Scale bars represent 10 mm (a-b), 50 mm (f-g) and 100 mm (c-e).
text-fig. 17. Lateral view of the braincase, illustrating states for several braincase characters, a, basal ornithischian Lesothosaurus diagnosticus; redrawn from Sereno (1991Z?). B, Troödon formosus; based on Currie and Zhao (1993a); the paroccipital process of Troödon is shown in cross-section to illustrate the internal pneumatic cavity within this bone. Abbreviations: atr, anterior tympanic recess; bpt, basipterygoid process; boc, basioccipital; bsp, basisphenoid; bt, basal tuber; ep, episthotic; f, frontal; fo, fenestra ovalis; ic, foramen for the entrance of the vidian canal for the internal carotid; jf, jugular foramen; Is, laterosphenoid; mf, metotic fissure; o, orbital facet on the frontal; oc, occipital condyle; op, opisthotic; osp, orbitosphenoid; pa, parietal; pn, pneumatic openings or cavities; pop, paroccipital process; pro, prootic; ps, parasphenoid; pspc, parasphenoid capsule; ptf, posttemporal foramen; vcm, exit of the vena capitis medialis; Roman numbers refer to the foramina for the exits of cranial nerves. Scale bars represent 10 mm. in The interrelationships and evolution of basal theropod dinosaurs
text-fig. 17. Lateral view of the braincase, illustrating states for several braincase characters, a, basal ornithischian Lesothosaurus diagnosticus; redrawn from Sereno (1991Z?). B, Troödon formosus; based on Currie and Zhao (1993a); the paroccipital process of Troödon is shown in cross-section to illustrate the internal pneumatic cavity within this bone. Abbreviations: atr, anterior tympanic recess; bpt, basipterygoid process; boc, basioccipital; bsp, basisphenoid; bt, basal tuber; ep, episthotic; f, frontal; fo, fenestra ovalis; ic, foramen for the entrance of the vidian canal for the internal carotid; jf, jugular foramen; Is, laterosphenoid; mf, metotic fissure; o, orbital facet on the frontal; oc, occipital condyle; op, opisthotic; osp, orbitosphenoid; pa, parietal; pn, pneumatic openings or cavities; pop, paroccipital process; pro, prootic; ps, parasphenoid; pspc, parasphenoid capsule; ptf, posttemporal foramen; vcm, exit of the vena capitis medialis; Roman numbers refer to the foramina for the exits of cranial nerves. Scale bars represent 10 mm.
10 MHz reference CW measured same as 5 MHz WWV
<p>This is a supplement to file K4BSE 34.124 -84.203 5 MHz.csv submitted last week, just after the frequency measurement period. I'd wondered about some jumps in frequency error I saw in my earlier submission (see xlxs file attached of the original frequency measurement run), so in this test I measured frequency error in exactly the same way, except that I was measuring a 10 MHz signal from a rubidium stabilized frequency source. The receiver was still stabilized by a GPSDO. I see some similar-magnitude frequency jumps here (note change in vertical scale). Also some frequency drifts is seen between some of the jumps, consistent with frequency drift in the test data submitted previously. I presume the jumps are due to the frequency calibration jumps in the K3's local oscillator. As best I can tell, the frequency of the K3 in the locked mode is determined by measurement of the frequency of an external 10 MHz oscillator, which is then used to calculate a correction to the tuned frequency of the radio. The jumps of a fraction of a Hz are consistent with the stated frequency accuracy of the radio when locked to a good reference (eg., the GPSDO used).</p>
FIGURE 2 in A new species of Pomponema Cobb, 1917 (Nematoda: Cyatholaimidae) from Northeast of Brazil, with reference to the taxonomic status of the genera Parapomponema Ott, 1972 and Propomponema Ott, 1972
FIGURE 2. Pomponema veronicae sp. n., holotype male MNRJ-NEMA48. A: overview; B: lateral view of anterior end, showing amphideal fovea, head setae and lateral punctations of cuticle; C: buccal cavity showing dorsal tooth, pairs of small subventral teeth and pairs of denticles; D: lateral differentiation of cuticle and pharynx; E: lateral differentiation of cuticle; F: lateral view of posterior end, showing precloacal supplements, spicule, gubernaculum, caudal glands and tail; G: precloacal supplements; H: spicule and gubernaculum.
FIGURE 3 in A new species of Pomponema Cobb, 1917 (Nematoda: Cyatholaimidae) from Northeast of Brazil, with reference to the taxonomic status of the genera Parapomponema Ott, 1972 and Propomponema Ott, 1972
FIGURE 3. Pomponema veronicae sp. n., holotype male MNRJ-NEMA48. A: overview; B: lateral view of anterior end, showing head setae, buccal cavity with dorsal tooth (1) and pairs of small subventral teeth (2); C: buccal cavity showing pairs of denticles; D: lateral differentiation of cuticle; E: lateral view of posterior end, showing precloacal supplements (1), spicules and gubernaculum (2), and tail; F: precloacal supplements (1), spicules and gubernaculum (2).
FIGURE 6 in A new species of Pomponema Cobb, 1917 (Nematoda: Cyatholaimidae) from Northeast of Brazil, with reference to the taxonomic status of the genera Parapomponema Ott, 1972 and Propomponema Ott, 1972
FIGURE 6. Comparison of spicules and gubernaculum of Pomponema veronicae sp. n. with the most closely related species of Pomponema. A: Pomponema veronicae sp. n.; B: P. hastatum; C: P. macrospirale. Drawings have been modeled in the same scale on those provided in the original descriptions (Ott, 1972).
FIGURE 5 in A new species of Pomponema Cobb, 1917 (Nematoda: Cyatholaimidae) from Northeast of Brazil, with reference to the taxonomic status of the genera Parapomponema Ott, 1972 and Propomponema Ott, 1972
FIGURE 5. Pomponema veronicae sp. n., paratype female MNRJ-NEMA49. A: overview; B: lateral view of anterior end, showing amphideal fovea and lateral punctations of cuticle; C: buccal cavity showing dorsal tooth (1) and pairs of small subventral teeth (2); D: reproductive system showing vulva; E: lateral view of posterior end, showing anus.
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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.