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FIGURE 13 in Acanthosaura phuketensis (Squamata: Agamidae), a new long-horned tree agamid from southwestern Thailand
FIGURE 13. Map of Thailand showing the type locality of Acanthosaura phuketensis sp. nov. (black dot). Courtesy of W. Sodob.
FIGURE 11 in Acanthosaura phuketensis (Squamata: Agamidae), a new long-horned tree agamid from southwestern Thailand
FIGURE 11. Live subadult female Acanthosaura phuketensis sp. nov. in situ at Ban Bangrong, Phuket Island, southwestern Thailand. Photo by P. Samphanthamit.
FIGURE 10 in Acanthosaura phuketensis (Squamata: Agamidae), a new long-horned tree agamid from southwestern Thailand
FIGURE 10. Live adult female Acanthosaura phuketensis sp. nov. in situ at Ban Bangrong, Phuket Island, southwestern Thailand. Photo by P. Samphanthamit.
FIGURE 9 in Acanthosaura phuketensis (Squamata: Agamidae), a new long-horned tree agamid from southwestern Thailand
FIGURE 9. Live subadult male Acanthosaura phuketensis sp. nov., eating a grasshopper on a tree in situ at Ban Bangrong, Phuket Island, southwestern Thailand. Photo by P. Samphanthamit.
FIGURE 8 in Acanthosaura phuketensis (Squamata: Agamidae), a new long-horned tree agamid from southwestern Thailand
FIGURE 8. Live adult male Acanthosaura phuketensis sp. nov., asleep on a branch in situ at Ban Bangrong, Phuket Island, southwestern Thailand. Photo by P. Samphanthamit.
FIGURE 7 in Acanthosaura phuketensis (Squamata: Agamidae), a new long-horned tree agamid from southwestern Thailand
FIGURE 7. Live adult male Acanthosaura phuketensis sp. nov. in situ at the type locality of Cyrtodactylus ranongensis in Suk Samran District, Ranong Province, southwestern Thailand. Photo by M. Sumontha.
FIGURE 5b in Acanthosaura phuketensis (Squamata: Agamidae), a new long-horned tree agamid from southwestern Thailand
FIGURE 5b. Ventral view of preserved Acanthosaura phuketensis sp. nov. subadult male paratype QSMI 1166. Photo by O. S. G. Pauwels.
FIGURE 3a in Acanthosaura phuketensis (Squamata: Agamidae), a new long-horned tree agamid from southwestern Thailand
FIGURE 3a. Dorsal view of preserved Acanthosaura phuketensis sp. nov. adult female paratype PSUZC-RT 2012.5. Photo by O. S. G. Pauwels.
FIGURE 1a in Acanthosaura phuketensis (Squamata: Agamidae), a new long-horned tree agamid from southwestern Thailand
FIGURE 1a. Lateral view of preserved Acanthosaura phuketensis sp. nov. adult male holotype. Photo by O. S. G. Pauwels. FIGURE 1b. Ventral view of preserved Acanthosaura phuketensis sp. nov. adult male holotype. Photo by O. S. G. Pauwels.
FIGURE 6b in Acanthosaura phuketensis (Squamata: Agamidae), a new long-horned tree agamid from southwestern Thailand
FIGURE 6b. Ventral view of preserved Acanthosaura phuketensis sp. nov. subadult male paratype PSUZC-RT 2012.6. Photo by O. S. G. Pauwels.
FIGURE 4a in Acanthosaura phuketensis (Squamata: Agamidae), a new long-horned tree agamid from southwestern Thailand
FIGURE 4a. Dorsal view of preserved Acanthosaura phuketensis sp. nov. adult female paratype THNHM 22543. Photo by O. S. G. Pauwels.
FIGURE 2 in Acanthosaura phuketensis (Squamata: Agamidae), a new long-horned tree agamid from southwestern Thailand
FIGURE 2. Left head side of preserved adult male paratype Acanthosaura phuketensis sp. nov. IRSNB 2681. Photo by O. S. G. Pauwels.
and metatarsal trichobothria as well as the bristles and the tibial and metatarsal bristleshaped hairs are drawn but no normal hairs; 6) retrolateral aspect of the left retroclaw IV; 7) genital area in front of the epigastral furrow in which no epiandrous gland spigots are recognizable. Not all of the hairs anteriorly of the pit are drawn; 8) outline of the anterior spinnerets, ventral aspect; 9) retrolateral aspect of the right pedipalpus; 10) prolateral aspect of the right pedipalpus. Only two of the long retrolateral bristle-shaped cymbial hairs are drawn; 11) ventral aspect of the right pedipalpus; 12) slightly different retroventral aspects of the distal part of the right pedipalpus. C = conductor, E = embolus, M = median apophysis, O = proventral-distal outgrowth of the pedipalpal tibia. Scale bars 0.5 mm in figs. 1-2 and 5, 0.05 in fig. 4 and 6, 0.1 in fig. 7, 0.2 in the remaining figs; in On European Spiders Of The Nominal Families Liocranidae, Miturgidae And Zoridae (Araneae), With Descriptions Of New Taxa
and metatarsal trichobothria as well as the bristles and the tibial and metatarsal bristleshaped hairs are drawn but no normal hairs; 6) retrolateral aspect of the left retroclaw IV; 7) genital area in front of the epigastral furrow in which no epiandrous gland spigots are recognizable. Not all of the hairs anteriorly of the pit are drawn; 8) outline of the anterior spinnerets, ventral aspect; 9) retrolateral aspect of the right pedipalpus; 10) prolateral aspect of the right pedipalpus. Only two of the long retrolateral bristle-shaped cymbial hairs are drawn; 11) ventral aspect of the right pedipalpus; 12) slightly different retroventral aspects of the distal part of the right pedipalpus. C = conductor, E = embolus, M = median apophysis, O = proventral-distal outgrowth of the pedipalpal tibia. Scale bars 0.5 mm in figs. 1-2 and 5, 0.05 in fig. 4 and 6, 0.1 in fig. 7, 0.2 in the remaining figs;
Coarse-grained Simulation data (part 2 of 2) for "Long-chain GM1 gangliosides alter transmembrane domain registration through interdigitation"
<p>Coarse-grained simulation data for the paper "Long-chain GM1 gangliosides alter transmembrane domain registration through interdigitation", Biochimica et Biophysica Acta (BBA) - Biomembrane Volume 1859, Issue 5, May 2017, Pages 870–87, DOI: 10.1016/j.bbamem.2017.01.033</p> <p>The simulations were performed using GROMACS 5.0.x [1]. The Martini force field [2,3] was employed.</p> <p>This part (2/2) of the upload contains data for the 10 replica simulations of the systems with GM1 with a normal tail and of the systems with a smaller concentration (1.5%) of GM1 with an extended tail. Trajectories, each 10 microseconds long and stored every 1ns, are given in xtc format. A common run input file for each type of system is given in the tpr format for analysis, although the initial structures of the replicas are different. These files are compatible with GROMACS 5. A common index file in ndx format and a common topology in top format are given for each system type. Simulation parameters, common for all simulated systems, are given in the mdp file. The itp files can be obtained from the Martini homepage http://cgmartini.nl/ </p> <p>The file names denote what kind of tail was used (normal vs. extended), the concentration of GM1 (1.5% (1) vs. 6% (6)), and the replica simulations are numbered from 1 to 10. For the systems without GM1 (NoGM1), the concentration is obviously not given, and there are only 8 replicas (see part 1).</p> <p>Part 1 of this upload is available at https://doi.org/10.5281/zenodo.831672.</p> <p>[1] M.J. Abraham et al., GROMACS: High performance molecular simulations through multi-level parallelism from laptops to supercomputers. SoftwareX, 2015, 1–2, pp. 19–25, DOI: 10.1016/j.softx.2015.06.001 </p> <p>[2] S.J. Marrink et al., The MARTINI Force Field:  Coarse Grained Model for Biomolecular Simulations. J. Phys. Chem. B, 2007, 111, pp 7812–7824, DOI:<strong> </strong>10.1021/jp071097f</p> <p>[3] C.A. López et al., Martini Force Field Parameters for Glycolipids. J. Chem. Theory Comput., 2013, 9, pp 1694–1708, DOI: 10.1021/ct3009655 </p>
Long-time Delays in Induced Earthquakes Caused by Low-Permeability Bodies: Insights from the Xinfengjiang Reservoir, China
<p>This version adds waveforms of the catalog earthquakes from 2014 to 2018.</p>
Datasets used in "Stomatal conductances influences interannual variability and long-term changes in regional cumulative plant uptake of ozone"
Model archived fields for surface ozone, effective stomatal conductance, and leaf area index corresponding to Clifton, O. E., Lombardozzi, D. L., Fiore, A. M., Paulot, F., & Horowitz, L. W., (2020). Stomatal conductance influences interannual variability and long-term changes in regional cumulative plant uptake, Environmental Research Letters.
Long-term climate trends and urbanization reveal human impacts and decoupling of dissolved organic carbon quantity and composition in streams
<p>This repository contains data, R code, graphical objects, and outputs in Kelley et al. (2025) entitled <strong><span lang="EN-US">Climate Change and Urbanization Decouple Dissolved Organic Carbon Quantity and Composition in Streams</span></strong><span lang="EN-US"> accepted for publication in <em>Global Biogeochemical Cycles</em></span><span lang="EN-US">. </span><a href="https://doi.org/10.1029/2025GB008534">https://doi.org/10.1029/2025GB008534</a></p> <p><span lang="EN-US">In this finalized repository, we provide a detailed meta data file (1_repository_meta_data.xlsx) containing lists and descriptions of all data files, variables, figures, and scripts within.</span> Note that previous versions contained water quality parameters for forms of nitrogen and phosphorus, which have been removed from this final version. These parameters were neither used in any analyses in this work nor underwent QA/QC protocols; thus, we suggest caution in their use from previous versions.</p> <p>Additionally, this repository contains a publication license for a graphical object created using the BioRender platform.</p>
Long-term demographic data on the red-cockaded woodpecker
<p>In cooperative breeding systems, inclusive fitness theory predicts that non-breeding helpers more closely related to the breeders should be more willing to provide costly alloparental care, and thus have more impact on breeder fitness. In the red-cockaded woodpecker (<em>Dryobates borealis</em>), most helpers are the breeders' earlier offspring, but helpers do vary within groups in both relatedness to the breeders (some even being unrelated) and sex, and it can be difficult to parse their separate impacts on breeder fitness. Moreover, most support for inclusive fitness theory has been positive associations between relatedness and behavior, rather than actual fitness consequences. We used functional linear models to evaluate the per capita effects of helpers of different relatedness on eight breeder fitness components measured for up to 41 years at three sites. In support of inclusive fitness theory, helpers more related to the breeding pair made greater contributions to six fitness components. However, male helpers made equal contributions to increasing pre-fledging survival regardless of relatedness. These findings suggest that both inclusive fitness benefits and other, direct benefits may underlie helping behaviors in the red-cockaded woodpecker. Our results also demonstrate the application of an underused statistical approach to disentangle a complex ecological phenomenon.</p>
FIGURE 11. Unornamented stomatocysts with a long collar. A. Stomatocyst 44 Pang & Wang. B. Stomatocyst 134 Duff & Smol. C–D. Stomatocyst 41 Duff & Smol. E. Stomatocyst 45 Pang & Wang. F. Stomatocyst 46 in Chrysophycean stomatocysts from the Aershan Geological Park (Inner Mongolia), China
FIGURE 11. Unornamented stomatocysts with a long collar. A. Stomatocyst 44 Pang & Wang. B. Stomatocyst 134 Duff & Smol. C–D. Stomatocyst 41 Duff & Smol. E. Stomatocyst 45 Pang & Wang. F. Stomatocyst 46 Pang & Wang. Scale bar = 2 µm.
FIGURES 2–4. Megalyra baltica Poinar and Shaw n in Megalyra baltica Poinar and Shaw n. sp. (Hymenoptera: Megalyridae), a long-tailed wasp from Baltic amber
FIGURES 2–4. Megalyra baltica Poinar and Shaw n. sp. in Baltic amber. 2. Forewing. Bar = 0.72 mm. 3. Hind wing. Bar = 0.66 mm. 4. Antenna. Bar = 0.63 mm.
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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)
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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.