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Figure 1 in Comparison of Coleoptera emergent from various decay classes of downed coarse woody debris in Great Smoky Mountains National Park, USA
Figure 1. Map of collection locations in Great Smoky Mountains National Park. Primary forest sites: 1) Laurel Falls; 2) Porters Creek; 3) Albright Grove. Secondary forest sites: 4) Tremont; 5) Sugarlands Quiet Walkway; 6) Greenbrier.
Figures 15–20. Habitus images. 15 in Comparison of Coleoptera emergent from various decay classes of downed coarse woody debris in Great Smoky Mountains National Park, USA
Figures 15–20. Habitus images. 15) Urographis fasciatus (Degeer) (Cerambycidae: Lamiinae). 16) Analeptura lineola Say (Cerambycidae: Lepturinae). 17) Trachysida mutabilis (Newman) (Cerambycidae: Lepturinae). 18) Cerylon castaneum Say (Cerylonidae). 19) Mychocerus striatus (Sen Gupta and Crowson) (Cerylonidae). 20) Philothermus glabriculus (LeConte) (Cerylonidae).
Molecular Determinants and Pharmacological Analysis for a Class of Competitive Non-transported Bicyclic Inhibitors of the Betaine/GABA Transporter BGT1: Modeling Data
<p>This archive contains the modeling data for the study <a href="https://www.frontiersin.org/articles/10.3389/fchem.2021.736457/full">"Molecular Determinants and Pharmacological Analysis for a Class of Competitive Non-transported Bicyclic Inhibitors of the Betaine/GABA Transporter BGT1"</a> (doi: 10.3389/fchem.2021.736457).</p> <p>The following data sets are available:</p> <ul> <li>Induced fit docking results of all mentioned compounds in the study: <br> ifd_hBGT1_occ_clustering_all_compounds.zip<br> </li> <li>MD simulations of bicyclo-GABA and compound 1 (100ns, 3 replica):<br> MD_simulation_bicyclo-GABA_run1.zip<br> MD_simulation_bicyclo-GABA_run2.zip<br> MD_simulation_bicyclo-GABA_run3.zip<br> MD_simulation_cmd1_run1.zip<br> MD_simulation_cmd1_run2.zip<br> MD_simulation_cmd1_run3.zip</li> </ul> <p>A detailed description of the methods is available in the aforementioned publication.</p> <p> </p> <p>The compound numbering in the uploaded files differs from the compound numbering in the mentioned study:</p> <p> </p> <p>study / upload</p> <p>bicyclo-GABA / cmd4</p> <p>1 / IIa</p> <p>2 /8-2</p> <p>3 / 8-3</p> <p>4a / 7-1</p> <p>4b / 7-2</p> <p>4c / 7-3</p> <p> </p> <p> </p> <p> </p> <p> </p> <p> </p> <p> </p>
Fig. 14 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico
Fig. 14. Additive tree (phenogram), based on Mahalanobis D2 distances (table 13), depicting meristic resemblance among nine groups of Aspidoscelis tesselata. Distances (similarities) between groups are computed by adding lengths of nodes between groups of interest. Terminal nodes represent the nine groups, and internal nodes represent horizontal distances between clusters. As an interpretation example, the resemblance between Conchas 6CE and Conchas 1CE is 7.2 + 3.2 + 2.2 + 2.8 + 5.6 = 21.0, while the resemblance between Conchas 6CE and Macho EC is 7.2 + 1.0 + 1.9 + 3.1 = 13.2.
Fig. 3 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico
Fig. 3. Electrophoretic phenotypes of sACOH, a monomeric enzyme, from liver homogenates of nine specimens of A. tesselata of pattern class CE from Conchas Lake State Park, New Mexico. Letters below gel identify allozymes based on alleles present (table 3), and the genotype of each lizard is listed on the right. Lanes for individual lizards are labeled beside their patterns on the gel. Anode is to the right.
Fig. 11 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico
Fig. 11. Pattern of multivariate morphological variation among Aspidoscelis tesselata of pattern classes C (N = 44), E (N = 32), and New Mexico D (N = 5) from the vicinity of Sumner Lake State Park, De Baca County, New Mexico. Canonical variate scores were derived from a canonical variate analysis using meristic characters identified in table 10.
Fig. 2 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico
Fig. 2. Electrophoretic phenotypes of GPI, a dimeric enzyme, from erythrocyte hemolysates of six specimens of Aspidoscelis. Letters below gel identify allozymes based on alleles present (table 3), and the genotype of each lizard is listed on the right. Note the very slight difference in migration between the products of the ballele versus callele. Lanes for individual lizards are labeled beside their patterns on the gel as follows: TESC, A. tesselata of pattern class CE from Conchas Lake State Park, New Mexico; and TESE, A. tesselata of pattern class E from Sandoval County, New Mexico. Anode is to the right.
Fig. 1 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico
Fig. 1. Geographic relationships among four northern collecting localities of Aspidoscelis tesselata of color pattern classes C, New Mexico D, and E and convenience classes CE and EC. Color patterns found at the four sites are (1) Conchas Lake State Park: CE and New Mexico D; (2) Sumner Lake State Park: C, New Mexico D, and E; (3) Puerto de Luna: E; and (4) Arroyo del Macho: EC.
Fig. 7 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico
Fig. 7. Color pattern variation in Aspidoscelis tesselata of pattern class CE from the vicinity of Conchas Lake State Park, San Miguel County, New Mexico. Morphological subgroup 6CE: A (RU 0002, 93 mm SVL); B (RU 0029, 96 mm SVL); morphological subgroup 1CE: C (RU 0013, 95 mm SVL); D (RU 0030, 89 mm SVL); E (RU 0021, 95 mm SVL); morphological subgroup 8CE: F (RU 0027, 86 mm SVL).
Fig. 4 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico
Fig. 4. Electrophoretic phenotypes of MPI, a monomeric enzyme, from liver homogenates of 11 specimens of Aspidoscelis. Letters below gel identify allozymes based on alleles present (table 3), and the genotype of each lizard is listed on the right. Lanes for individual lizards are labeled beside their patterns on the gel (with genotype) as follows: NEOTESA, B, and C, different pattern classes of the triploid A. neotesselata from Colorado; TESC and D, A. tesselata of pattern classes CE and D from Conchas Lake State Park, New Mexico; TESE, A. tesselata of pattern class EC from Arroyo del Macho, New Mexico; TESF, A. dixoni from New Mexico; TESF × PUN, triploid hybrid of A. dixoni × A. tigris punctilinealis from New Mexico; and TESG and H, A. dixoni of two pattern classes from Texas. Anode is to the right.
FIG. 54 in A revision of the supraspecific classification of the subclass Calcaronea (Porifera, class Calcarea)
FIG. 54. — Surface view of the solid calcareous skeleton of Petrobiona massiliana, showing terminal spines of the sclerodermites (sc) and partially entrapped spicules (sp) (SEM). Scale bar: 50 µm (from Vacelet 1991).
FIG. 52 in A revision of the supraspecific classification of the subclass Calcaronea (Porifera, class Calcarea)
FIG. 52. — Diagram of dissociated spicules of Tulearinia stylifera Vacelet, 1977 (light micrograph); A, superficial diactines; B, microdiactines; C, perioscular triactines; D, triactines; E, tetractines from the basal network; F, tetractine from canals. Scale bars: A, D, E, 50 µm; B, C, 15 µm; F, 20 µm (from Vacelet 1977).
FIG. 53 in A revision of the supraspecific classification of the subclass Calcaronea (Porifera, class Calcarea)
FIG. 53. — Diagram of the organization of Petrobiona massiliana Vacelet & Lévi, 1958. Abbreviations: cx, cortical skeleton; ch, choanosome; ct, tracts of storage cells; d, solid calcareous skeleton; e, parasitic excavating sponge (from Vacelet 1964).
FIG. 49 in A revision of the supraspecific classification of the subclass Calcaronea (Porifera, class Calcarea)
FIG. 49. — Transverse section of Plectroninia hindei Kirkpatrick, 1900 (light micrograph). Abbreviations: p, papilla; o, osculum; c, choanosome; cs, cortical skeleton; lt, large fused tetractines of the choanoskeleton; st, small fused tetractines of the choanoskeleton. Scale bar: 330 µm (from Pouliquen & Vacelet 1970).
FIG. 50 in A revision of the supraspecific classification of the subclass Calcaronea (Porifera, class Calcarea)
FIG. 50. — View of the choanoskeleton of Plectroninia sp., showing two layers of tetractines fused by their basal actines (SEM). Scale bar: 50 µm (from Vacelet 1991).
FIG. 46 in A revision of the supraspecific classification of the subclass Calcaronea (Porifera, class Calcarea)
FIG. 46. — Trichogypsia villosa (Carter, 1871); A, a diagram of a transverse section of the body wall, showing a pit-like cavity and a canal parallel to the external surface that bears conules containing very densely arranged parallel diactines; B, diactines of the cortical conules; C, diactines of the internal reticular skeleton; D, diactines that line the pit-like cavity.
FIG. 45 in A revision of the supraspecific classification of the subclass Calcaronea (Porifera, class Calcarea)
FIG. 45.— Diagram of pugioles and microdiactines;A, Baeria gladiator; B, Lamontia zona; C, Baeria nivea; D, Baeria ochotensis.
FIG. 43 in A revision of the supraspecific classification of the subclass Calcaronea (Porifera, class Calcarea)
FIG. 43. — Diagram of the formation of choanocyte chambers of diamorphies during the process of reconstitution from dissociat- ed cells; drawing from original micrographs by Peixinho (1980); A, pre-sycon stage of Grantia compressa; B, pre-leucon stage in Baeria nivea. Scale bar: A, 26 µm; B, 45 µm.
FIG. 44 in A revision of the supraspecific classification of the subclass Calcaronea (Porifera, class Calcarea)
FIG. 44. — Pugioles (p) in an exhalant canal (ex) of Baeria nivea (Johnston, 1842). Scale bar: 90 µm.
FIG. 40 in A revision of the supraspecific classification of the subclass Calcaronea (Porifera, class Calcarea)
FIG. 40. — Skeletal arrangement in a longitudinal section of Lelapia australis Gray, 1867. Abbreviations: a, atrium; dc, dermal cortex; dt, dermal tuft of triactines and slender diactines; fi, spicular fibres formed of tuning-fork-shaped triactines; gc, atrial cortex. Scale bar: 350 µm (from Dendy 1894).
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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.