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3,484 results for “Plastics”
Figure 1 in Observation of Megachile saulcyi (Guérin-Méneville, 1844) (Hymenoptera: Megachilidae) using plastic for nest construction in Chile
Figure 1. Site where Megachile saulcyi was found in central Chile. / Sitio donde se encontró a Megachile saulcyi en Chile central.
Figure 1 in Limited thermal plasticity in high mountain tropical water bears
Figure 1. The environmental temperature is depicted in black while the moss temperature is shown in green. Temperatures were recorded every minute from October 18th to November 16th, 2023. Throughout the day, temperatures were not stable. The average environmental temperature was 14.7 °C, ranging from a minimum of 9.3 °C to a maximum of 25.6 °C. The average moss temperature was 14.6 °C, ranging from a minimum of 9.6 °C to a maximum of 23.1 °C.
Fig. 1 in Evaluation of plastic packaging for prevention of damage to wheat by Trogoderma granarium (Coleoptera: Dermestidae), and suitability of phosphine fumigation
Fig. 1. Damage (holes and scratches) with openings created by Trogoderma granarium in plastic packaging: Lengths of openings in holes, (A) measurement line = 2,495 μm in opaque polyethylene, and (B) measurement line = 1,943 μm in polypropylene. Lengths of openings in scratches, (C) measurement line = 688 μm in opaque polyethylene, and (D) measurement line = 146 μm in polypropylene.
Fig. 1 in Influence of feeding plasticity on the fitness of small Neotropical characids
Fig. 1. Study area in the Pantanal of Mato Grosso do Sul State, Brazil. A and B indicate the sampling sites in lagoons associated with the Miranda River.
Fig. 2 in Influence of feeding plasticity on the fitness of small Neotropical characids
Fig. 2. Food resources (% IAi) consumed by Hyphessobrycon eques, Odontostilbe pequira, Psellogrammus kennedyi and Serrapinnus calliurus, in the lagoons A and B (Ain, aquatic invertebrates; Tin, terrestrial invertebrates; Tes, Testacea; FSc, fish scale; Pla, plant; Alg, algae; Det, detritus).
Fig. 11 in Three-dimensional elasto-plastic soil modelling and analysis of sauropod tracks
Fig. 11. Vertical displacement after circular and pressure-shaped curvilinear quadrilateral. A. Vertical displacement after a circular pressure. B. Vertical displacement after a pressure-shaped curvilinear quadrilateral with concave and convex alternate sides.
Fig. 10 in Three-dimensional elasto-plastic soil modelling and analysis of sauropod tracks
Fig. 10. Deformed mesh and vertical displacement in layer 1, scaled 20 times. A. Deformed small footprint, mesh after footfall (surface of layer 1); scaled up 20 times. B. Vertical displacements after footfall (surface of layer 1); scale in mm. C. Vertical displacements after footfall (surface of layer 2); scale in mm. D. Deformed mesh after the footfall (surface of layer 1); at true scale.
Fig. 9 in Three-dimensional elasto-plastic soil modelling and analysis of sauropod tracks
Fig. 9. Deformed mesh and vertical displacement in layer 2. A. Deformed big footprint, mesh after footfall (surface of layer 2); at true scale. B. Vertical displacements after the footfall (surface of layer 2); scale in mm.
Fig. 8 in Three-dimensional elasto-plastic soil modelling and analysis of sauropod tracks
Fig. 8. Deformed mesh and vertical displacement in layer 1. A. Deformed mesh after a footfall in a plastic layer 1; at true scale. B. Vertical displacement after the footfall (surface of the plastic layer 1); scale in mm.
Fig. 7 in Three-dimensional elasto-plastic soil modelling and analysis of sauropod tracks
Fig. 7. Results of the calculation model. A. Calculation model for big footprint after the footfall. B. Deformed mesh (at true scale) after the footfall (surface of layer 1). C. Detail of simulation model with phreatic level. D. Vertical displacement after the footfall (surface of layer 1); scale in mm. E. Position of the vertical section. F. Vertical displacements of the section shown in E.
Fig. 5. Track 95 in Three-dimensional elasto-plastic soil modelling and analysis of sauropod tracks
Fig. 5. Track 95 in layer VIII-B of the Miraflores I tracksite, Berriasian (Early Cretaceous), Soria, Spain, showing footprint section. Scale 120 mm.
Fig. 4. Tracks 86 and 95 in Three-dimensional elasto-plastic soil modelling and analysis of sauropod tracks
Fig. 4. Tracks 86 and 95 in the Miraflores I tracksite. A. Plan view of the autopod, without toe marks, that formed tracks 86 and 95; horizontal line indicates the zone where the section was made. B. Section of the track/ footprint to be reproduced, with mean values of the vertical displacements and measurements of thickness, both in mm.
Fig. 3. Scheme showing traces from layer VIII-B in Three-dimensional elasto-plastic soil modelling and analysis of sauropod tracks
Fig. 3. Scheme showing traces from layer VIII-B of Miraflores I tracksite and view of the tracks 86 and 95.
Fig. 2 in Three-dimensional elasto-plastic soil modelling and analysis of sauropod tracks
Fig. 2. Stratigraphic column of the Miraflores I tracksite, showing the layers containing dinosaur tracks (Roman numerals).
Fig. 9 in Ecophenotypic plasticity versus evolutionary trends-morphological variability in Upper Jurassic bivalve shells from Portugal
Fig. 9. Scatter plot of resilifer number over ligament length in Isognomon. The two groups that correspond to lithostratigraphy are clearly visible. Numbers in squared brackets refer to Fig. 2.
Fig. 8 in Ecophenotypic plasticity versus evolutionary trends-morphological variability in Upper Jurassic bivalve shells from Portugal
Fig. 8. Box plots of size for the three target taxa. A. Size of Arcomytilus based on log transformed geometric means of length and height. B. Size of Isognomon based on log transformed ligament length. C. Size of Eomiodon based on log transformed shell length. Arrangement of boxes corresponding more or less to their stratigraphic succession, from left to right. Numbers in squared brackets refer to Fig. 2.
Fig. 12 in Ecophenotypic plasticity versus evolutionary trends-morphological variability in Upper Jurassic bivalve shells from Portugal
Fig. 12. PCA plot of shell shape in Arcomytilus, grouped according to rib number in steps of 25 ribs and displayed as convex hulls.
Fig. 7 in Ecophenotypic plasticity versus evolutionary trends-morphological variability in Upper Jurassic bivalve shells from Portugal
Fig. 7. Scatter plots of log transformed values of height over length for the three target taxa. A. Arcomytilus. B. Isognomon. C. Eomiodon. Numbers in squared brackets refer to Fig. 2.
Fig. 6 in Ecophenotypic plasticity versus evolutionary trends-morphological variability in Upper Jurassic bivalve shells from Portugal
Fig. 6. Measured distances in the three target taxa. A. Arcomytilus. B. Isognomon. C. Eomiodon. Abbreviations: H, height; L, length; LL, ligament length. Arrow indicates turning point of growth.
Fig. 5 in Ecophenotypic plasticity versus evolutionary trends-morphological variability in Upper Jurassic bivalve shells from Portugal
Fig. 5. Specimens of neomiodontid bivalve Eomiodon securiformis (Sharpe, 1850) from the Upper Jurassic of Portugal. A–C. Sobral member, Late Kimmeridgian, E Arranhó. A. Hinge plates of left and right valve. GML 25915. B. Interior of right valve, showing hinge arrangement and parts of the muscle scars. GML 25916. C. Left valve view of articulated specimen. GML 25917. D. Articulated, strongly elongated, gerontic specimen. Sobral member, Late Kimmeridgian, Santa Cruz. GML 25918. E. Small articulated specimen with clearly visible commarginal lamellae. Alcobaça formation, Early Kimmeridgian, Vestiaria. GML 25919. F. Articulated gerontic specimen with ventrally elongated shell. Alcobaça formation, Early Kimmeridgian, Salgados. GML 25920. G. Short, rounded, articulated specimen. Sobral member, Late Kimmeridgian, E Arranhó. GML 25921. H. Large, high, and short specimen. Sobral member, Late Kimmeridgian, Porto das Barcas. GML 25922.
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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.