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Fig. 5 in Integrative approach to resolve the Calotes mystaceus Duméril & Bibron, 1837 species complex (Squamata: Agamidae)

Fig. 5. Calotes bachae Hartmann et al., 2013. A. Holotype (ZFMK 88935, adult male), general view from above. B. Holotype, lateral view. C. Living holotype from Cat Tien National Park, Vietnam.

Fig. 3 in Integrative approach to resolve the Calotes mystaceus Duméril & Bibron, 1837 species complex (Squamata: Agamidae)

Fig. 3. Principal component analyses results for the morphologically examined specimens. Details of Eigenvalues and explained variance are given in Table 3.

Fig. 2. The Bayesian consensus tree basedon 988 in Integrative approach to resolve the Calotes mystaceus Duméril & Bibron, 1837 species complex (Squamata: Agamidae)

Fig. 2. The Bayesian consensus tree basedon 988 bp of mitochondrial DNA (12S rRNA and COI) shows six distinctlineages within Calotes mystaceus. Node support in terms of Bayesian posterior probabilities is indicated by circles at nodes (nodes with a BPP ≥ 0.90 are white, BPP ≥ 0.95 are grey, BPP ≥ 0.99 are black, values <0.90 arenot marked). Outgroup (Calotes versicolor) notshown for clarity. Numbers in parentheses behind taxa refer to localities mapped in Fig. 1.

Fig. 1 in Integrative approach to resolve the Calotes mystaceus Duméril & Bibron, 1837 species complex (Squamata: Agamidae)

Fig. 1. Geographic distribution of examined specimens of the Calotes mystaceus complex. Colors correspond to the identified OTUs. Diamonds mark the type localities of the species described herein. Records with a bold margin were also included in the phylogenetic analyses. Imprecise (i.e., country-level) records are marked with a question mark. Detailed localities are: Calotes bachae: Vietnam: Dong Nai Prov.: Cat Tien National Park (1); Dong Nai Nature Reserve (2); Bu Gia Map National Park (3); Kon Tum (4); Trung Khanh (5); Cambodia: Banlung (7); Calotes goetzi sp. n.: Cambodia: Phnom Kulen National Park (8); Kulen Promtep Wildlife Sanctuary (9); Laos: Muang Phon Hong (10); Luang Prabang (11); Muang Pak Lay (12); Thailand: Sakon Nakhon Prov. (13); Lam Dom Noi River (14); Khon Buri (15); Nakhon Ratchasima (16); Dilang (17); Ban Nam Len (18); Lom Sak (19); Ban Bueng (20); Khlong Luang (21); Cha-am (22); Ban Phai (23); Kwai River bridge (24); Ban Dong Noi (25); Phitsanulok Prov. (26); Nan Prov. (27); Chiang Mai Prov. (28); Fang (33); Myanmar: Kawkareik (30); Mudon (31); Karen Hills (32); Parsa Wildlife Sanctuary (29); Kyaitong Township (34, 35); Inle Lake Wetland Sanctuary (36, 37); Taunggyi (38); Pindaya (39); Panlaung and Padalin Cave Wildlife Sanctuary (40); Mandalay-Yangon road (41); Minsontaung Wildlife Sanctuary (42); Popa Mountain Park (43); Mandalay (44); Shwebo (45); Bhamo (46); Indawgyi Lake (47); "Pegu" (54, see discussion in text); China: Baihualing (48); Longyang (49, 50); Liuku-Longling road (51); Liuku (52); Liuku-Fugong road (53); Calotes mystaceus: Myanmar: "Pegu" (54; see discussion in text); Kyaiktiyo Pagoda (56, 57); Taungoo (58); Letpein village (59); Hlawga National Park (60); Ngapudaw township (61); Ngayokekaung village (62); Calotes vindumbarbatus sp. n.: Myanmar: Gat Shang Yang village (63); Hepu village (64); Linpha village (65); Swekawngaw (66); Calotes geissleri sp. n.: Myanmar: Alaungdaw Kathapa National Park (67, 68); Mauk village (69, 70); Natzang village (71); Simggial village (72); India: Nagaland: Kohima (73).

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Seismic source location with a match field processing approach during the RESOLVE dense seismic array experiment on the Glacier d'Argentiere

This deposit contains the data set we used in our paper ‘Dynamic imaging of glacier structures at high-resolution using source localization with a dense seismic array’. The paper is in review for GRL and a preprint can be found here: <a href="http://dx.doi.org/10.1002/essoar.10507953.1">10.1002/essoar.10507953.1</a>. The dataset present here contains 34 files named ‘beam_15423_jd***.h5’. These files correspond to the output of the matched field processing for each day. They are in .h5 format and we provide a matlab code (read_MFP_data.m) to read these files. These files can be read with any other language since they are in . h5. In linux you can use h5dump –A filename.h5 and you can see the content of each files.   More information on how the MFP process is conducted can be found in on the <a href="https://lecoinal.gricad-pages.univ-grenoble-alpes.fr/resolve/">website </a>dedicated to this aspect or on our paper. The whole procedure and associated codes is provided on the <a href="http://lecoinal.gricad-pages.univ-grenoble-alpes.fr/resolve/">lecoinal.gricad-pages.univ-grenoble-alpes.fr/resolve/</a>. We also deliver with this deposit one day of seismic data  <a href="https://zenodo.org/api/files/873ccbe8-814d-4202-90ae-e115aab1942d/ZO_2018_121.h5?versionId=c59d2014-a6e1-43c5-96a6-91ee9a6b89ce">ZO_2018_121.h5 </a>that can be used to test our MFP process. The data corresponds to the signal measured for 24 hours at each of the 98 sensors with a sampling rate of 500 Hz. More information on these seimsic signals can be found on our <a href="https://lecoinal.gricad-pages.univ-grenoble-alpes.fr/resolve/">website </a>and the whole seimsic dataset can be found here <a href="https://seismology.resif.fr/networks/#/ZO__2018">https://seismology.resif.fr/networks/#/ZO__2018</a>. Detailed for downloading the dataset should be search on our website.   Other dataset linked to this project are: <ul> <li>Nanni, Ugo, Gimbert, Florent, Roux, Phillipe, & Lecointre, Albanne. (2020). DATA of "Resolving the 2D temporal evolution of subglacial water flow with dense seismic array observations." [Data set]. Zenodo. <a href="https://doi.org/10.5281/zenodo.4024660">https://doi.org/10.5281/zenodo.4024660 </a></li> <li>Nanni, Gimbert, Roux, Helmstetter, Garambois, Lecointre, Walpersdorf, Jourdain, Langlais, Laarman, Lindner, Sergenat, Vincent, & Walter. (2020). DATA of the RESOLVE Project (https://resolve.osug.fr/) [Data set]. In Seismological Research Letters (Version v0). Zenodo. <a href="https://doi.org/10.5281/zenodo.3971815">https://doi.org/10.5281/zenodo.3971815 </a></li> </ul> This dataset is also linked to two other study: Observing the subglacial hydrology network and its dynamics with a dense seismic array:  <a href="https://doi.org/10.1073/pnas.2023757118">https://doi.org/10.1073/pnas.2023757118</a> A Multi‐Physics Experiment with a Temporary Dense Seismic Array on the Argentière Glacier, French Alps: The RESOLVE Project <a href="https://doi.org/10.1785/0220200280">https://doi.org/10.1785/0220200280</a>         Do not hesitate to contact us if you would like to try this approach an another dataset.

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Reference data and analysis software for "Four-color single-molecule imaging with engineered tags resolves the molecular architecture of signaling complexes in the plasma membrane"

Reference data set for the single molecule co-tracking analysis presented in "Four-color single-molecule imaging with engineered tags resolves the molecular architecture of signaling complexes in the plasma membrane". Corresponding author for further inquiries: Prof. Dr. Jacob Piehler University of Osnabrück, Department of Biology/Chemistry, Division of Biophysics, Barbarastr. 11, 49076 Osnabrück, Germany https://www.biophysik.uni-osnabrueck.de/

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Time-Resolved Photoionization Detection of a Single Er3+ Ion in Silicon

The data used for generating the plots in the manuscript and supporting information.

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Wall Resolved Fluid-Structure Interaction Numerical Simulation of a Modern Wind Turbine Blade

Wall-resolved fluid-structure interaction (FSI) numerical simulations of the NREL 5 MW wind turbine blade are compared using two FSI approaches. The first method is based on high-fidelity Nektar++/SHARPy FSI framework, where the fluid governing equations are solved using high-order spectral/hp element method and the turbulent flow is resolved using Large Eddy Simulation (LES) on thick strips, while large-deformation dynamics of the structure are mod- elled using a geometrically exact nonlinear composite beam finite-element model. Thick strip method for the fluid reduces the computational cost by considering a series of smaller domains, each of which has a finite thickness in the spanwise direction. Hence, the overall flow over the blade is treated with a sectional approach, where in each of these sections, strips, the 3D flow is reconstructed locally. Tip-loss correction is used to compensate for the sectional approach over the blade. The second FSI approach is based on OpenFoam/Calculix coupling, where the second-order unstructured finite volume method approach is used for solving the three-dimensional flow equations and the flow turbulence is captured us- ing the k-ω SST model. The structural dynamics are modeled via second-order finite element method using standard solid elements. Effects of the solution fidelity on the prediction of aerodynamic forces as well as on the full three-dimensional flow modelling over the blade versus sectional representation of flow over the blade while incorporating the local three- dimensionality in each section and tip-correction are discussed. Further, significance of two approaches on modelling the slender blade, one using the beam mode and the other utilizing the full 3D solution of structure is addressed. Finally, assessment of computational cost and scalability of the two approaches are presented and discussed.

Fig. 11 in UCE Phylogenomics Resolves Major Relationships Among Ectaheteromorph Ants (Hymenoptera: Formicidae: Ectatomminae, Heteroponerinae): A New Classification For the Subfamilies and the Description of a New Genus

Fig. 11. Lateral view of propodeum, showing: A) Propodeal spiracle separated from declivity margin by a distance longer than its diameter (Typhlomyrmex lavra); B) Propodeal spiracle close to the declivous face of propodeum (Holcoponera relicta—USNMENT00412058). Photos by Gabriela Camacho (A) and Jeffrey Sosa-Calvo; available from www.antweb.org (Antweb 2021).

Fig. 10 in UCE Phylogenomics Resolves Major Relationships Among Ectaheteromorph Ants (Hymenoptera: Formicidae: Ectatomminae, Heteroponerinae): A New Classification For the Subfamilies and the Description of a New Genus

Fig. 10. Lateral view of gaster, showing: A) Second gastric segment (IV abdominal) relatively straight (Gnamptogenys acuminata—USNMENT00441095); B) Second gastric segment (IV abdominal) slightly arched ventrally (Poneracantha mecotyle—CASENT0281530). Photos by Jeffrey Sosa-Calvo (A) and Zach Lieberman (B); available from www.antweb.org (Antweb 2021).

Fig. 8 in UCE Phylogenomics Resolves Major Relationships Among Ectaheteromorph Ants (Hymenoptera: Formicidae: Ectatomminae, Heteroponerinae): A New Classification For the Subfamilies and the Description of a New Genus

Fig. 8. Lateral view of gaster, showing: A) Second gastral (IV abdominal) sternite not strongly reduced in relation to the tergite; dorsal profile of gaster gently convex, so that the apex of gaster is only discretely directed ventrally (Gnamptogenys acuminata—USNMENT00441095); B) Second gastral (IV abdominal) sternite strongly reduced in relation to the tergite; dorsal profile of gaster extremely convex, so that the gaster is strongly directed ventrally and anterad (Alfaria minuta—CASENT0281213). Photos by Jeffrey Sosa-Calvo (A) and Estella Ortega (B); available from www.antweb.org (Antweb 2021).

Fig. 5 in UCE Phylogenomics Resolves Major Relationships Among Ectaheteromorph Ants (Hymenoptera: Formicidae: Ectatomminae, Heteroponerinae): A New Classification For the Subfamilies and the Description of a New Genus

Fig. 5. Lateral view of pronotum, showing: A) Pronotal tubercles present; mesonotum prominent, separated from propodeum by a deep transversal suture (Ectatomma tuberculatum—CASENT0173380); B) Pronotal tubercles or projections absent; mesonotum not prominent, forming a continuous profile with propodeum (Holcoponera striatula—CASENT0173386). Photos by April Nobile; available from www.antweb.org (Antweb 2021).

Fig. 7 in UCE Phylogenomics Resolves Major Relationships Among Ectaheteromorph Ants (Hymenoptera: Formicidae: Ectatomminae, Heteroponerinae): A New Classification For the Subfamilies and the Description of a New Genus

Fig. 7. Frontal view of head, showing: A) Expanded frontal lobes (Alfaria falcifera—CASENT0179971); B) Occipital lobes absent (Gnamptogenys continua— CASENT0173383). Photos by Erin Prado (A) and April Nobile (B); available from www.antweb.org (Antweb 2021).

Fig. 1 in UCE Phylogenomics Resolves Major Relationships Among Ectaheteromorph Ants (Hymenoptera: Formicidae: Ectatomminae, Heteroponerinae): A New Classification For the Subfamilies and the Description of a New Genus

Fig. 1. In lateral view, workers of the Ectatomminae genera, showing the morphological diversity within the clade. (A) Acanthoponera mucronata (CASENT0173540), (B) Alfaria minuta (CASENT0281213), (C) Ectatomma planidens (CASENT0173379), (D) Gnamptogenys acuminata (USNMENT00441095), (E) Heteroponera panamensis (CASENT0106021), (F) Holcoponera ammophila (CASENT0281512), (G) Poneracantha mecotyle (CASENT0281530), (H) Rhytidoponera metallica (CASENT0172345), (I) Stictoponera biroi (CASENT0172380), (J) Typhlomyrmex rogenhoferi (CASENT0173390). See Fig. 3 for images of Boltonia microps. Images by April Nobile, Estella Ortega, Michael Branstetter, Zach Lieberman, and Jeffrey Sosa-Calvo; available from www.antweb.org (Antweb 2021).

Fig. 3 in UCE Phylogenomics Resolves Major Relationships Among Ectaheteromorph Ants (Hymenoptera: Formicidae: Ectatomminae, Heteroponerinae): A New Classification For the Subfamilies and the Description of a New Genus

Fig. 3. Worker of Boltonia microps in A) frontal view; B) dorsal view; and C) lateral view. Images by April Nobile (CASENT0173544); available from www.antweb. org (Antweb 2021).

Fig. 2 in UCE Phylogenomics Resolves Major Relationships Among Ectaheteromorph Ants (Hymenoptera: Formicidae: Ectatomminae, Heteroponerinae): A New Classification For the Subfamilies and the Description of a New Genus

Fig. 2. Phylogeny of the subfamily Ectatomminae based on phylogenomic analyses of the UCE 90% complete data set (150 taxa). Figure is based on IQ-Tree besttree searches with ultrafast bootstrap (UFB) frequencies of less than 100% mapped onto the respective nodes. UFB searches consisted of 1000 replicates.The eleven larger ectatommine lineages are indicated. Branch color indicates the biogeographical range of the species.Taxa marked with asterisk (*) were classified in Gnamptogenys prior to this revision and those with double asterisk (**) were included in Heteroponera prior to this revision. See Supplementary material for the 75% complete matrix (Supp Fig. S1 [online only]). Ant photos show heads in frontal view of, from top to bottom:Gnamptogenys acuminata (USNMENT00441095), Typhlomyrmex rogenhoferi (CASENT0004700), Holcoponera striatula (CASENT0106042), Alfaria simulans (CASENT0603729), Poneracantha rastrata (CASENT0281223), Stictoponera biroi (CASENT0281519), Rythidoponera metallica (CASENT0172345), Ectatomma lugens (USNMENT00445341), Heteroponera brounii (CASENT0172105), Acanthoponera mucronata (CASENT0173540), and Boltonia microps (CASENT0173544). Images by April Nobile, Jeffrey Sosa-Calvo, Zach Lieberman,Will Ericson, Michael Branstetter, and Estella Ortega; available from www.antweb.org (Antweb 2021).

Fig. 4 in UCE Phylogenomics Resolves Major Relationships Among Ectaheteromorph Ants (Hymenoptera: Formicidae: Ectatomminae, Heteroponerinae): A New Classification For the Subfamilies and the Description of a New Genus

Fig. 4. Dorsal view of head, showing: A) Cephalic median longitudinal carina present, extending from the anterior clypeal margin to the vertex (Acanthoponera minor—CASENT0178699); B) Cephalic median longitudinal carina not extending from the anterior clypeal margin to the vertex (Ectatomma tuberculatum— CASENT0173380); C) Cephalic median longitudinal carina absent (Holcoponera striatula—CASENT0173386). Photos by April Nobile; available from www. antweb.org (Antweb 2021).

Fig. 9 in UCE Phylogenomics Resolves Major Relationships Among Ectaheteromorph Ants (Hymenoptera: Formicidae: Ectatomminae, Heteroponerinae): A New Classification For the Subfamilies and the Description of a New Genus

Fig. 9. Dorsal view of mesosoma, showing: A) Promesonotal suture absent (Gnamptogenys acuminata—USNMENT00441095); B) Promesonotal suture feeble, never interrupting dorsal mesosomal sculpture (Poneracantha banksi—INBIOCRI001281007); C) Promesonotal suture well marked, totally interrupting dorsal mesosomal sculpture (Holcoponera moelleri—CASENT0173384). Photos by Jeffrey Sosa-Calvo (A), Estella Ortega (B), and April Nobile (C); available from www. antweb.org (Antweb 2021).

Fig. 6 in UCE Phylogenomics Resolves Major Relationships Among Ectaheteromorph Ants (Hymenoptera: Formicidae: Ectatomminae, Heteroponerinae): A New Classification For the Subfamilies and the Description of a New Genus

Fig. 6. Dorsal view of pronotum, showing: A) Pronotum and mesonotum separated by a distinct suture (Rhytidoponera abdominalis—CASENT0281333); B) Pronotum and mesonotum continuous with a discrete groove (Gnamptogenys stellae—CASENT0281227). Photos by Cerise Chen (A) and Estella Ortega (B) available from www.antweb.org (Antweb 2021).