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Fig. 2. Eusurbus altus (Walker), 1849, ♂ (ANIC No. 29-008742): (a) dorsal; (b) lateral; (c) head, dorsal; (d) flagellum; (e) wing; (f ) head, frontal; (g) head, profile. Scale bars = 1 mm. This figure is published in colour in the online edition of this journal, which can be accessed via http://booksandjournals.brillonline. com/content/journals/1876312x.
Fig. 2. Eusurbus altus (Walker), 1849, ♂ (ANIC No. 29-008742): (a) dorsal; (b) lateral; (c) head, dorsal; (d) flagellum; (e) wing; (f ) head, frontal; (g) head, profile. Scale bars = 1 mm. This figure is published in colour in the online edition of this journal, which can be accessed via http://booksandjournals.brillonline. com/content/journals/1876312x.
Fig. 3. Eusurbus altus (Walker), 1849, ♀ (ANIC No. 29-008754): (a) dorsal; (b) lateral; (c) head, dorsal; (d) head, lateral; (e) head, frontal; (f ) head, profile. Scale bars = 1 mm. This figure is published in colour in the online edition of this journal, which can be accessed via http://booksandjournals.brillonline.com/ content/journals/1876312x. This figure is published in colour in the online edition of this journal, which can be accessed via http://booksandjournals.brillonline.com/content/journals/1876312x.
Fig. 3. Eusurbus altus (Walker), 1849, ♀ (ANIC No. 29-008754): (a) dorsal; (b) lateral; (c) head, dorsal; (d) head, lateral; (e) head, frontal; (f ) head, profile. Scale bars = 1 mm. This figure is published in colour in the online edition of this journal, which can be accessed via http://booksandjournals.brillonline.com/ content/journals/1876312x. This figure is published in colour in the online edition of this journal, which can be accessed via http://booksandjournals.brillonline.com/content/journals/1876312x.
Fig. 16. Zentamyia nigracinctus (Roberts, 1929), ♂ holotype (ANIC No. 29-009843): (a) dorsal; (b) lateral; (c) head dorsal; (d) flagellum; (e) head, frontal; (f ) head, profile. Scale bars = 1 mm. This figure is published in colour in the online edition of this journal, which can be accessed via http:// booksandjournals.brillonline.com/content/journals/1876312x.
Fig. 16. Zentamyia nigracinctus (Roberts, 1929), ♂ holotype (ANIC No. 29-009843): (a) dorsal; (b) lateral; (c) head dorsal; (d) flagellum; (e) head, frontal; (f ) head, profile. Scale bars = 1 mm. This figure is published in colour in the online edition of this journal, which can be accessed via http:// booksandjournals.brillonline.com/content/journals/1876312x.
Figure 2. Stylopallene longicauda, A, B, male dorsal and lateral views of trunk; C, male carrying juveniles, D, mating pair, male dorsal; E, swimming; F, plummeting on completion of the swimming phase.
Figure 2. Stylopallene longicauda, A, B, male dorsal and lateral views of trunk; C, male carrying juveniles, D, mating pair, male dorsal; E, swimming; F, plummeting on completion of the swimming phase.
Figure 3. Stylopallene tubirostris, A, B, male, dorsal and lateral views of trunk; C, female, anterior view of cephalon; D, scape process; E, live specimen; F, juveniles on male; G, juvenile; H, exuviae attached to male oviger.
Figure 3. Stylopallene tubirostris, A, B, male, dorsal and lateral views of trunk; C, female, anterior view of cephalon; D, scape process; E, live specimen; F, juveniles on male; G, juvenile; H, exuviae attached to male oviger.
Figure 1. Stylopallene cheilorhynchus, A, B, male, dorsal and lateral views of trunk; C, female, anterior view; D, live specimen; E, protonymphon on ovigers; F, discarded exuvia.
Figure 1. Stylopallene cheilorhynchus, A, B, male, dorsal and lateral views of trunk; C, female, anterior view; D, live specimen; E, protonymphon on ovigers; F, discarded exuvia.
FIgS. 23–25. Urodacus butleri, n. sp., holotype ♂ (WAM T85141), dextral leg illustrating spiniform macrosetae. 23. Basitarsus, ventral aspect. 24, 25. Telotarsus, ventral and lateral aspects. Scale bar = 0.5 mm.
FIgS. 23–25. Urodacus butleri, n. sp., holotype ♂ (WAM T85141), dextral leg illustrating spiniform macrosetae. 23. Basitarsus, ventral aspect. 24, 25. Telotarsus, ventral and lateral aspects. Scale bar = 0.5 mm.
FIgS. 9–14. Urodacus butleri, n. sp., holotype ♂ (WAM T85141). 9. Metasomal segment II, lateral aspect. 10, 11. Metasomal segment V, lateral and ventral aspects. 12. Metasomal segment IV, lateral aspect. 13, 14. Telson, lateral and ventral aspects. Scale bars = 0.5 mm.
FIgS. 9–14. Urodacus butleri, n. sp., holotype ♂ (WAM T85141). 9. Metasomal segment II, lateral aspect. 10, 11. Metasomal segment V, lateral and ventral aspects. 12. Metasomal segment IV, lateral aspect. 13, 14. Telson, lateral and ventral aspects. Scale bars = 0.5 mm.
Heteromudas bicolor Hardy, male genitalia: 82, ventral view; 83, dorsal view; 84, lateral view. in The American Genera of Mydidae (Diptera), with the Description of three new Genera and two new Species
Heteromudas bicolor Hardy, male genitalia: 82, ventral view; 83, dorsal view; 84, lateral view.
A Self-Adaptive Deep Learning Method for Automated Eye Laterality Detection Based on Color Fundus Photography
<p>The data for "A Self-Adaptive Deep Learning Method for Automated Eye Laterality Detection Based on Color Fundus Photography", including original image data and labels, DL model files, training logs and validation results.</p> <p><strong>Content</strong>:</p> <p>- <strong>Ex1_Preprocessing</strong> # the first experiment: preprocessing methods comparison</p> <p> - <strong>history</strong> # validation results of different metrics of models </p> <p> - <strong>log</strong> # training record of models. Read by TensorBoard</p> <p> - <strong>model</strong> # model file. Read by Keras</p> <p>- <strong>Ex2_Self-adaptive model</strong> # the second experiment: development of eye laterality detection model</p> <p> - <strong>data</strong> # serialized image data, including data and ground-truth label. Read by Python Pickle package.</p> <p> - <strong>Xy.h5</strong> # training data</p> <p> - <strong>test_Xy.h5</strong> # testing data</p> <p> - <strong>history</strong> # validation results of different metrics of models </p> <p> - <strong>log</strong> # training record of models. Read by TensorBoard</p> <p> - <strong>model</strong> # model file. Read by Keras</p> <p> - <strong>with_adaptive</strong> # with self-adaptive strategy</p> <p> - <strong>without_adaptive</strong> # without self-adaptive strategy</p> <p>For code review, please see: <a href="https://github.com/keepgallop/Eye-laterality-detection">https://github.com/keepgallop/Eye-laterality-detection</a></p> <p>For more information, please contact liuchi_email@foxmail.com</p> <p> </p> <p> </p> <p> </p>
Data: The effect of external lateral stabilization on the use of foot placement to control mediolateral stability in walking and running
<p>Data and code for Mahaki et al. (2019): The effect of external lateral stabilization on the use of foot placement to control mediolateral stability in walking and running (<a href="https://doi.org/10.7717/peerj.7939">https://doi.org/10.7717/peerj.7939</a>).</p> <p>The Gas, Force, and Optotrak data.rar folder contains three subfolders as follows:</p> <p><strong>Gasdata2</strong> - contains all oxygen data, plus a scripts to run the data.</p> <p> - Subjectxx - folder with oxygen data</p> <p> - MainMohammadRunning_EC - script to analyze the oxygen data.</p> <p> - EC_walkRun_Stat - script to statistically test the hypotheses in terms of energetic cost. The results have been presented in supplementary material (<strong>Fig. S5.</strong>)</p> <p><strong>KinData</strong> - contains all kinematic and kinetic data (one folder per subject)</p> <p> - Marker.xlsx - info on which markers were placed where</p> <p> - Pointers.xlsx - info on which pointer trials contain which virtual markers</p> <p> - Trials.xlsx - info on which files contain which conditions</p> <p> - Subjectxx - folder with all the data.</p> <p> - The *.ndf files contain the kinematics (can be read with readndf.m, available in a subfolder of the VU 3d model (see below)</p> <p> - The *.afp files contain the raw voltage data from the force plates. These can be converted to forces and moments using the function FBW_dualbelt.m, available in a subfolder of the VU 3d model (see below).</p> <p> - The _HS.mat files contain calculated events (see script A below), and are normal matlab files.</p> <p><strong>Software</strong> - contains all code used to get from the kinematic data to outcome variables, script were ran as:</p> <p> - A_Main_Heelstrikes - script which calculates heelstrikes, and prompts the user to check these. Results are saved in the same folder (and under same name, but with extension HS.mat) as original data.</p> <p> - B_Main_Calculate_step - script which was used to calculate main outcomes for each subject and condition. results of this script are stored in foot_placement_thorax.mat and used in subsequent scripts.</p> <p> - C_Combine_Test_Legs - script which was used to statistically investigate the effect of leg and speed on R<sup>2</sup> time series (lines 67-69). The results have been presented in Supplementary Material file (<strong>Fig. S1.</strong>).</p> <p> - D_main_plot_WalkRun_normalOnly - script which was used to check our second hypothesis which was the comparison between normal walking and running in terms of foot placement strategy. The results have been presented in <strong>Fig 4. & 5.</strong>.</p> <p> - E_main_plot_WalkRun - script which was used to check our third and fourth hypotheses which we investigated the effect of external lateral stabilization on R<sup>2</sup> values in walking and running (hypothesis 3) and differences of external lateral stabilization effect between walking and running (i.e. mode of locomotion X condition interaction, hypothesis 4) during swing phase. The results have been presented in <strong>Fig 5. and Fig 7.</strong>.</p> <p> - SW_SWvariability_WalkRun - script which was used to check our hypotheses in terms of step width and step width variability. The results have been presented in <strong>Fig 6</strong>.</p> <p> - F_Supplementary_main_plot_run - script which was used to compare R<sup>2</sup> values between running trials (speed effect) and the results have been presented in supplementary material (<strong>Fig .S2.</strong>).</p>
Figure. Aedeagus of Anthobium fusculum Erichson, 1839 (left – dorsal view, right – lateral view). in Updated list of the subfamily Omaliinae (Coleoptera: Staphylinidae) from Kazakhstan with some new records
Figure. Aedeagus of Anthobium fusculum Erichson, 1839 (left – dorsal view, right – lateral view).
Table I in Revisiting Potter Cove, King George Island, Antarctica, 12 years later: new observations of marine benthic diatoms
<p>Table I: (continued)</p><table><tbody><tr><th>Species</th><th>ZDDƎ</th><th>ZDIs</th></tr></tbody><tbody><tr><th><i>Grammatophora angulosa</i> Ehrenberg</th><td>r</td><td>–</td></tr><tr><th><i>Grammatophora angulosa</i> var. <i>islandica</i> (Ehrenberg)</th><td>r</td><td>–</td></tr><tr><th>Grunow</th></tr><tr><th><i>Gyrosigma arcuatum</i> (Donkin) Sterrenburg</th><td>–</td><td>r</td></tr><tr><th><b><i>Gyrosigma fasciola</i> (Ehrenberg) Grif</b> fi th <i>et</i> Henfrey</th><td>c</td><td>c</td></tr><tr><th><b><i>Gyrosigma</i> cf. <i>obscurum</i> (W. Smith) Grif</b> fi th <i>et</i> Henfrey</th><td>–</td><td>c</td></tr><tr><th><i>Halamphora holsatica</i> (Hustedt) Levkov e</th><td>vr</td><td>–</td></tr><tr><th><i>Hippodonta hungarica</i> (Grunow) Lange-Bertalot, Met-</th><td>r</td><td>–</td></tr><tr><th>zeltin <i>et</i> Witkowski</th></tr><tr><th><i>Licmophora abbreviata</i> Agardh</th><td>f</td><td>–</td></tr><tr><th><i>Licmophora antarctica</i> Carlson</th><td>f</td><td>f</td></tr><tr><th><i>Licmophora belgicae</i> Peragallo</th><td>–</td><td>f</td></tr><tr><th><i>Licmophora decora</i> Heiden</th><td>r</td><td>–</td></tr><tr><th><i>Licmophora gracilis</i> (Ehrenberg) Grunow</th><td>f</td><td>f</td></tr><tr><th><i>Licmophora luxuriosa</i> Heiden</th><td>–</td><td>r</td></tr><tr><th><i>Lyrella hennedyi</i> (W. Smith) Stickle <i>et</i> D. G. Mann</th><td>–</td><td>r</td></tr><tr><th><i>Melosira adeliae</i> Manguin</th><td>r</td><td>r</td></tr><tr><th><i>Melosira sol</i> (Ehrenberg) Kützing</th><td>–</td><td>f</td></tr><tr><th><i>Minidiscus trioculatus</i> (Taylor) Hasle</th><td>r</td><td>–</td></tr><tr><th><i>Navicula</i> cf. <i>cancellata</i> Donkin</th><td>c</td><td>f</td></tr><tr><th><i>Navicula directa</i> (Smith) Brébisson</th><td>f</td><td>c</td></tr><tr><th><i>Navicula</i> cf. <i>perminuta</i> Grunow</th><td>c</td><td><b>c</b></td></tr><tr><th><b><i>Navicula</i> sp.</b> 1</th><td>vr</td><td><b>r</b></td></tr><tr><th><b><i>Navicula</i> sp.</b> 2</th><td>–</td><td>r</td></tr><tr><th><i>Nitzschia angularis</i> W. Smith</th><td>–</td><td>f</td></tr><tr><th><i>Nitzschia</i> cf. <i>australis</i> (Peragallo) A. Mann</th><td>vr</td><td>r</td></tr><tr><th><i>Nitzschia</i> cf. <i>gelida</i> Cleve <i>et</i> Grunow</th><td>–</td><td>r</td></tr><tr><th><i>Nitzschia hybrida</i> Grunow</th><td>r</td><td>c</td></tr><tr><th><i>Nitzschia mitchelliana</i> Greenleaf</th><td>–</td><td>r</td></tr><tr><th><i>Nitzschia</i> cf. <i>obtusa</i> W. Smith</th><td>–</td><td>r</td></tr><tr><th><i>Nitzschia pellucida</i> Grunow</th><td>r</td><td>–</td></tr><tr><th><i>Nitzschia sigma</i> (Kützing) W. Smith</th><td>–</td><td>r</td></tr><tr><th><i>Nitzschia tubicola</i> Grunow</th><td>r</td><td><b>–</b></td></tr><tr><th><b><i>Nitzschia</i> sp.</b> 1</th><td>r</td><td>–</td></tr><tr><th><i>Odontella litigiosa</i> (Van Heurck) Hoban</th><td>f</td><td>c</td></tr><tr><th><i>Paralia sulcata</i> (Ehrenberg) Cleve</th><td>–</td><td>vr</td></tr><tr><th><i>Parlibellus delognei</i> (Van Heurck) E. J. Cox</th><td>r</td><td>–</td></tr><tr><th><i>Parlibellus crucicula</i> (W. Smith) Witkowski, Lange-</th><td>–</td><td>f</td></tr><tr><th><b>Bertalot <i>et</i> Metzeltin</b></th></tr><tr><th><b><i>Parlibellus</i> sp.</b> 1</th><td>vr</td><td><b>–</b></td></tr><tr><th><b><i>Parlibellus</i> sp.</b> 2</th><td>r</td><td>–</td></tr><tr><th><i>Petroneis plagiostoma</i> (Grunow) D. G. Mann</th><td>c</td><td><b>c</b></td></tr><tr><th><b><i>Petroneis</i> sp.</b> 1</th><td>r</td><td><b>c</b></td></tr><tr><th><b><i>Petroneis</i> sp.</b> 2</th><td>r</td><td>–</td></tr><tr><th><i>Pinnularia quadratarea</i> (A. Schmidt) Cleve</th><td>f</td><td>c</td></tr><tr><th><i>Planothidium lanceolatum</i> (Brébisson <i>ex</i> Kützing)</th><td>r</td><td>–</td></tr><tr><th>Lange-Bertalot</th></tr><tr><th><i>Planothidium vicentii</i> Manguin</th><td>vr</td><td>–</td></tr><tr><th><i>Pseudogomphonema kamtschaticum</i> (Grunow) Medlin</th><td>f</td><td>f</td></tr><tr><th><i>Pleurosigma diversestriatum</i> Meister</th><td>–</td><td>r</td></tr><tr><th><i>Pleurosigma eudon</i> var. <i>kerguelensis</i> Heiden <i>et</i> Kolbe</th><td>vr</td><td>vr</td></tr><tr><th><i>Pleurosigma strigosum</i> W. Smith</th><td>–</td><td>c</td></tr><tr><th><i>Podosira stelliger</i> (Bailey) A. Mann</th><td>–</td><td>vr</td></tr><tr><th><i>Porosira glacialis</i> (Grunow) JØrgensen</th><td>–</td><td>f</td></tr><tr><th><i>Rhabdonema arcuatum</i> (Lyngbye) Kützing</th><td>–</td><td>r</td></tr><tr><th><i>Rhoicosphenia abbreviata</i> (Agardh) Lange-Bertalot</th><td>r</td><td><b>–</b></td></tr></tbody></table>
Table I in Revisiting Potter Cove, King George Island, Antarctica, 12 years later: new observations of marine benthic diatoms
<p>Table I: (continued)</p><table><tbody><tr><th>Species</th><th>ZDDƎ</th><th>ZDIs</th></tr></tbody><tbody><tr><th><i>Staurophora</i> sp.</th><td>–</td><td>r</td></tr><tr><th><i>Stellarima microtrias</i> (Ehrenberg) Hasle <i>et</i> Sims</th><td>–</td><td>f</td></tr><tr><th><i>Surirella fastuosa</i> (Ehrenberg) Ehrenberg</th><td>–</td><td>vr</td></tr><tr><th><i>Surirella</i> sp.</th><td>–</td><td>r</td></tr><tr><th><i>Synedra kerguelensis</i> Heiden</th><td>r</td><td>–</td></tr><tr><th><i>Synedropsis fragilis</i> (Manguin) Hasle, Medlin <i>et</i></th><td>r</td><td>–</td></tr><tr><th><b>Syvertsen</b></th></tr><tr><th><i>Synedropsis recta</i> Hasle, Medlin <i>et</i> Syvertsen</th><td>r</td><td>–</td></tr><tr><th><i>Synedropsis</i> sp.</th><td>–</td><td>f</td></tr><tr><th><i>Tetramphora rhombica</i> (Kitton) Stepanek <i>et</i> Kociolek f</th><td>vr</td><td>–</td></tr><tr><th><i>Thalassionema nitzschioides</i> (Grunow) Mereschkowsky</th><td>r</td><td>r</td></tr><tr><th><i>Thalassiosira eccentrica</i> (Ehrenberg) Cleve</th><td>–</td><td>r</td></tr><tr><th><i>Thalassiosira gracilis</i> (Karsten) Hustedt</th><td>r</td><td>f</td></tr><tr><th><i>Thalassiosira lentiginosa</i> (Janisch) Fryxell</th><td>vr</td><td>–</td></tr><tr><th><i>Thalassiosira maculata</i> Fryxell <i>et</i> Johansen</th><td>vr</td><td>–</td></tr><tr><th><i>Thalassiosira oliveriana</i> (O’ Meara) Makarova <i>et</i></th><td>–</td><td>r</td></tr><tr><th><b>Nikolajev</b></th></tr><tr><th><i>Thalassiosira ritscheri</i> (Hustedt) Hasle</th><td>vr</td><td>–</td></tr><tr><th><i>Thalassiosira tumida</i> (Janisch) Hasle</th><td>r</td><td>–</td></tr><tr><th><i>Thalassiosira</i> sp.</th><td>–</td><td>r</td></tr><tr><th><i>Trachyneis aspera</i> (Ehrenberg) Cleve</th><td>f</td><td>f</td></tr><tr><th><i>Trachyneis</i> cf. <i>robusta</i> Petit</th><td>r</td><td>–</td></tr><tr><th><i>Triceratium favus</i> Ehrenberg</th><td>–</td><td>r</td></tr><tr><th><i>Trigonium arcticum</i> (Brightwell) Cleve</th><td>–</td><td><b>r</b></td></tr></tbody></table><p><b>vr, very rare, few cells found; r, rare,</b> 1 <b>–</b> 5 <b>%; f, frequent,</b> 5 <b>–</b> 20 <b>%; c, common,></b> 20 <b>%; –, not observed. <sup>a</sup> Reported as <i>Amphora</i> cf. <i>fogediana</i> (Grunow) Lange-Bertalot in Al-Handal and Wulff (</b>2008 <b>a). <sup>b</sup> Reported as</b> <b><i>Caloneis</i> sp.</b> 1 <b>in Al-Handal and Wulff (</b>2008 <b>a). <sup>c</sup> Reported as <i>Cocconeis schuettii</i> Van Heurck in Al-Handal and Wulff (</b>2008 <b>a). <sup>d</sup> Reported as <i>Achnanthidium exigua</i> (Grunow) Lange-Bertalot in Al-Handal and Wulff (</b>2008 <b>a). <sup>e</sup> Reported as <i>Amphora holsatica</i> Husted in Al-Handal and Wulff (</b>2008 <b>a). <sup>f</sup> Reported as <i>Amphora rhombica</i> Kitton <i>ex</i> A. Schmidt in Al-Handal and Wulff (</b>2008 <b>a).</b></p>
Table I in Revisiting Potter Cove, King George Island, Antarctica, 12 years later: new observations of marine benthic diatoms
<p><b>Table I: Comparison of the occurrence of marine benthic diatoms in Potter Cove, King George Island, Antarctica in</b> 2003 <b>(Al-Handal and Wulff</b> 2008 <b>b) and</b> 2015 (present study).</p><table><tbody><tr><th>Species</th><th>ZDDƎ</th><th>ZDIs</th></tr></tbody><tbody><tr><th><i>Achnanthes bongrainii</i> (M. Peragallo) A. Mann</th><td>r</td><td>–</td></tr><tr><th><i>Achnanthes</i> cf. <i>groenlandica</i> (Cleve) Grunow</th><td>–</td><td>f</td></tr><tr><th><i>Actinocyclus actinochilus</i> (Ehrenberg) Simonsen</th><td>r</td><td>c</td></tr><tr><th><i>Actinocyclus curvatulus</i> Janisch</th><td>r</td><td>–</td></tr><tr><th><i>Amphora</i> cf. <i>eximia</i> Carter a</th><td>r</td><td>–</td></tr><tr><th><i>Amphora gourdonii</i> M. Peragallo</th><td>–</td><td>f</td></tr><tr><th><i>Amphora marina</i> W. Smith</th><td>f</td><td>f</td></tr><tr><th><i>Amphora</i> cf. <i>laevissima</i> Gregory</th><td>r</td><td>–</td></tr><tr><th><i>Amphora spectabilis</i> Gregory</th><td>r</td><td><b>–</b></td></tr><tr><th><b><i>Amphora</i> sp.</b> 1</th><td>–</td><td><b>r</b></td></tr><tr><th><b><i>Amphora</i> sp.</b> 2</th><td>–</td><td>r</td></tr><tr><th><i>Asteromphalus parvulus</i> Karsten</th><td>–</td><td>r</td></tr><tr><th><i>Biremis ambigua</i> (Cleve) D. G. Mann <i>Caloneis</i> sp. b</th><td>– vr</td><td>f r</td></tr><tr><th><i>Campyloneis frenguellii</i> Riaux-Gobin <i>et</i> Guerrero</th><td>–</td><td>f</td></tr><tr><th><i>Cocconeis antiqua</i> Tempère <i>et</i> Brun c</th><td>f</td><td>f</td></tr><tr><th><i>Cocconeis costata</i> Gregory</th><td>r</td><td>–</td></tr><tr><th><i>Cocconeis costata</i> var. <i>antarctica</i> Manguin</th><td>r</td><td>–</td></tr><tr><th><i>Cocconeis costata</i> var. <i>hexagona</i> Grunow</th><td>–</td><td>r</td></tr><tr><th><i>Cocconeis dallmannii</i> Al-Handal, Riaux-Gobin, Romero</th><td>–</td><td><b>r</b></td></tr><tr><th><b><i>et</i> Wulff</b></th></tr><tr><th><i>Cocconeis fasciolata</i> (Ehrenberg) Brown</th><td>r</td><td>f</td></tr><tr><th><i>Cocconeis hauniensis</i> Witkowski</th><td>vr</td><td>–</td></tr><tr><th><i>Cocconeis</i> cf. <i>imperatrix</i> A. Schmidt</th><td>r</td><td>c</td></tr><tr><th><i>Cocconeis matsii</i> (Al-Handal, Riaux-Gobin <i>et</i> A.Wulff)</th><td>–</td><td>f</td></tr><tr><th><b>Riaux-Gobin, Compère, Romero <i>et</i> Williams</b></th></tr><tr><th><i>Cocconeis melchioroides</i> Al-Handal, Riaux-Gobin,</th><td>–</td><td>r</td></tr><tr><th><b>Romero <i>et</i> Wulff</b></th></tr><tr><th><i>Cocconeis moronensis</i> A. Schmidt</th><td>vr</td><td>–</td></tr><tr><th><i>Cocconeis pinnata</i> Gregory <i>ex</i> Greville</th><td>r</td><td>–</td></tr><tr><th><i>Cocconeis scutellum</i> Ehrenberg</th><td>vr</td><td><b>–</b></td></tr><tr><th><b><i>Cocconeis</i> sp.</b> 1</th><td>vr</td><td><b>–</b></td></tr><tr><th><b><i>Cocconeis</i> sp.</b> 2</th><td>vr</td><td>–</td></tr><tr><th><b><i>Corethron pennatum</i> (Grunow) Osten</b> fi eld</th><td>r</td><td>f</td></tr><tr><th><i>Coscinodiscus asteromphalus</i> Ehrenberg</th><td>vr</td><td>–</td></tr><tr><th><i>Coscinodiscus radiatus</i> Ehrenberg</th><td>–</td><td>vr</td></tr><tr><th><i>Cylindrotheca closterium</i> (Ehrenberg) Reimann <i>et</i> Lewin</th><td>–</td><td>r</td></tr><tr><th><i>Diploneis smithii</i> (Brébisson) Cleve</th><td>r</td><td>r</td></tr><tr><th><i>Diploneis weiss</i> fl ogii (Schmidt) Cleve</th><td>–</td><td>vr</td></tr><tr><th><i>Diploneis</i> sp.</th><td>–</td><td>r</td></tr><tr><th><i>Entomoneis gigantea</i> Grunow</th><td>vr</td><td>r</td></tr><tr><th><i>Entomoneis kjellmanii</i> (Cleve) Poulin <i>et</i> Cardinal</th><td>f</td><td>r</td></tr><tr><th><i>Entomoneis paludosa</i> (W. Smith) Reimer</th><td>f</td><td>c</td></tr><tr><th><i>Entopyla ocellata</i> (Arnott) Grunow</th><td>r</td><td>f</td></tr><tr><th><i>Eucampia antarctica</i> (Castracane) Mangin</th><td>vr</td><td>–</td></tr><tr><th><i>Eunotia praerupta</i> Ehrenberg</th><td>vr</td><td>–</td></tr><tr><th><i>Fogedia</i> cf. <i>giffeniana</i> (Foged) Witkowski, Lange-</th><td>r</td><td>–</td></tr><tr><th><b>Bertalot, Metzeltin <i>et</i> Bafana</b></th></tr><tr><th><i>Fragilaria striatula</i> Lyngbye</th><td>–</td><td>f</td></tr><tr><th><i>Fragilariopsis cylindrus</i> (Grunow <i>ex</i> Cleve) Helmcke <i>et</i></th><td>–</td><td>r</td></tr><tr><th><b>Krieger</b></th></tr><tr><th><i>Fragilariopsis rhombica</i> (O’ Meara) Hustedt</th><td>r</td><td>–</td></tr><tr><th><i>Gogorevia parexigua</i> (Metzeltin <i>et</i> Lange-Bertalot) Kulikovskiy <i>et</i> Kociolek d</th><td>r</td><td><b>–</b></td></tr></tbody></table>
Experimental data for Dynamic cover effects in lateral bedrock channel bank abrasion: Experiment and model comparison
<p>Experimental data for bank erosion.xlsx contains the data used for the figures in the paper, and the distribution of bedrock bank erosion in the longitudinal direction in Run 1 - Run 18.</p>
Retrieving 2D laterally varying structures from multi-station surface wave dispersion curves using multiscale window analysis
<p>Here are the waveform data used in the Geophysical Journal International paper entitled "Retrieving 2D laterally varying structures from multi-station surface wave dispersion curves using multiscale window analysis". The dataset is used for the reader who wants to reproduce the result in the paper.</p>
Supplemental material to 'A variational rigid-block modelling approach to nonlinear elastic and kinematic analysis of failure mechanisms in historic masonry structures subjected to lateral actions'
<p>This repository contains the data necessary to reproduce the content of the article:</p> <blockquote> <p>A variational rigid-block modelling approach to nonlinear elastic and kinematic analysis of failure mechanisms in historic masonry structures subjected to lateral actions (2021). Earthquake Engineering & Structural Dynamics, 1–23. <a href="https://onlinelibrary.wiley.com/doi/full/10.1002/eqe.3512">https://doi.org/10.1002/eqe.3512</a></p> </blockquote> <p>The file <strong>01_Dataset.zip</strong> contains the dataset. The companion document <strong>00_Dataset_description.pdf </strong>describes the content of the dataset, guiding the analyst to its use in order to (i) reproduce the article's results and (ii) compare the article's results to new results brought by the analyst, e.g. by comparison with other numerical models.</p> <p>Version history</p> <p>v2: updated references in 00_dataset description.pdf </p>
Growth acceleration results in faster telomere shortening later in life
<p>There is a wealth of evidence for a lifespan penalty when environmental conditions influence an individual´s growth trajectory such that growth rate is accelerated to attain a target size within a limited time period. Given this empirically demonstrated relationship between accelerated growth and lifespan, and the links between lifespan and telomere dynamics, increased telomere loss could underpin this growth-lifespan trade. We experimentally modified the growth trajectory of nestling zebra finches (<i>Taeniopygia guttata</i>), inducing a group of nestlings to accelerate their growth between 7 and 15 days of age, the main phase of body growth. We then sequentially measured their telomere length in red blood cells at various time points from 7 days to full adulthood (120 days). Accelerated growth between 7 and 15 days was not associated with a detectable increase in telomere shortening during this period compared with controls. However, only in the treatment group induced to show growth acceleration, the rate of growth during the experimental period was positively related to the amount of telomere shortening between 15 and 120 days. Our findings provide evidence of a long-term influence of growth rate on later-life telomere shortening, but only when individuals have accelerated growth in response to environmental circumstances.</p>
Figure 1-2. Temnocerus species, lateral habitus. 1 in Central American Temnocerus Thunberg, 1815 (Coleoptera: Rhynchitidae)
Figure 1-2. Temnocerus species, lateral habitus. 1) T. potosi n.sp. 2) T. abdominalis (Voss).
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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International Brain Laboratory public data
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OpenNeuro
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