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Fig. 2 in Influence of plant direction, layer, and spacing on the infestation levels of Anthonomus eugenii (Coleoptera: Curculionidae) in open jalapeño pepper fields in North Florida
Fig. 2. Infestation and larval density of pepper weevil in 2017. Vertical bars are standard errors of the means.
Fig. 5 in Influence of plant direction, layer, and spacing on the infestation levels of Anthonomus eugenii (Coleoptera: Curculionidae) in open jalapeño pepper fields in North Florida
Fig. 5. Relationship between the infestation level and the fruit wall thickness (A) and single weight (B). Each data point represents the number of infested fruits per plant in each fruit wall thickness or weight (means ± SE). Line was fitted using linear regression analysis.
Fig. 1 in Influence of plant direction, layer, and spacing on the infestation levels of Anthonomus eugenii (Coleoptera: Curculionidae) in open jalapeño pepper fields in North Florida
Fig. 1. (a) Adult pepper weevil feeding on the stalk of a pepper fruit; (b) young and full grown larvae inside a pepper fruit; (c) pupa inside the fruit; and (d) adult weevil exit holes in pepper fruits.
Fig. 6 in Multiple infestations induce direct defense of maize to Tetranychus urticae (Acari: Tetranychidae)
Fig. 6. Number (mean ± SE) of live females (A, C2 = 7.39; df = 37; P <0.001), immature individuals (B, C2 = 2.14; df = 36; P <0.001), eggs (C, C2 = 2.14; df = 36; P <0.001), and dead females (D, C2 = 7.7; df = 36; P <0.001) of the two-spotted spider mite Tetranychus urticae on conspecific plus Spodoptera frugiperda infested conventional (white bars) and Bt (gray bars) maize plants. M = mite, C = caterpillar. *** = statistically significant (P <0.01).
Fig. 5 in Multiple infestations induce direct defense of maize to Tetranychus urticae (Acari: Tetranychidae)
Fig. 5. Number (mean ± SE) of live females (A, C2 = 29.5; df =37; P = 0.195), immature individuals (B, C2 = 39.1; df = 36; P = 0.670), eggs (C, C2 = 31.7; df = 36; P = 0.326), and dead females (D, C2 = 22.0; df = 37; P = 0.024) of the two-spotted spider mite Tetranychus urticae on conspecific (white bars) and conspecific plus Spodoptera frugiperda infested (gray bars) Bt maize plants. M = mite, C = caterpillar. ns = statistically insignificant, * = statistically significant (P <0.05).
Fig. 4 in Multiple infestations induce direct defense of maize to Tetranychus urticae (Acari: Tetranychidae)
Fig. 4. Number (mean ± SE) of live females (A, C2 = 7.65; df = 37; P <0.001), immature individuals (B, C2 = 2.60; df = 36; P <0.001), eggs (C, C2 = 2.14; df = 36; P <0.001), and dead females (D, C2 = 5.38; df = 37; P <0.001) of the two-spotted spider mite Tetranychus urticae on conspecific (white bars) and conspecific plus Spodoptera frugiperda infested (gray bars) conventional maize plants. M = mite, C = caterpillar. *** = statistically significant (P <0.01).
Fig. 3 in Multiple infestations induce direct defense of maize to Tetranychus urticae (Acari: Tetranychidae)
Fig. 3. Number (mean ± SE) of live females (A, C2 = 31.11; df = 37; P = 0.259), immature individuals (B, C2 = 27.67; df = 37; P = 0.133), eggs (C, C2 = 27.67; df = 36; P = 0.240), and dead females (D, C2 = 23.58; df = 37; P = 0.042) of the two-spotted spider mite Tetranychus urticae on infested conventional (30F35) (white bars) and Bt (30F35Hx) (gray bars) maize plants. ns = statistically insignificant, * = statistically significant (P <0.05).
Fig. 1 in Multiple infestations induce direct defense of maize to Tetranychus urticae (Acari: Tetranychidae)
Fig. 1. Number (mean ± SE) of live females (A, C2 = 45.2; df = 36; P = 0.861), immature individuals (B, C2 = 38.7; df = 37; P = 0.608), eggs (C, C2 = 38.1; df = 36; P = 0.624), and dead females (D, C2 = 29.7; df = 37; P = 0.203) of the two-spotted spider mite Tetranychus urticae on clean (white bars) and co-specific re-infested (gray bars) conventional maize plants (30F35). ns = statistically insignificant.
Fig. 7 in Multiple infestations induce direct defense of maize to Tetranychus urticae (Acari: Tetranychidae)
Fig. 7. Projection to principal component analysis based on the ions detected by electrospray ionization mass spectrometry of uninfested (C = o) and infested with Tetranychus urticae (C + Tu = ●) conventional maize; uninfested (Bt = Z) and infested with T. urticae (Bt + Tu = ■) Bt maize; infested with T. urticae and Spodoptera frungiperda (C + Tu + Sf = Δ) conventional maize; and infested with T. urticae and S. frungiperda (Bt + Tu + Sf = ▲) Bt maize, using the first 2 principal components (Dim) with explained variance in brackets
Fig. 2 in Multiple infestations induce direct defense of maize to Tetranychus urticae (Acari: Tetranychidae)
Fig. 2. Number (mean ± SE) of live females (A, C2 = 21.9; df = 37; P = 0.02), immature individuals (B, C2 = 40.9; df = 37; P = 0.698), eggs (C, C2 = 30.5; df = 37; P = 0.235), and dead females (D, C2 = 21.9; df = 37; P = 0.383) of the two-spotted spider mite, Tetranychus urticae, on clean (light gray bars) and co-specific re-infested (dark gray bars) Bt maize plants (30F35Hx). ns = statistically insignificant, * = statistically significant (P <0.05).
Figure 2 in Scientific Opinion on a notification (reference C/NL/09/02) for the placing on the market of the genetically modified carnation IFD-26407-2 with a modified colour, for import of cut flowers for ornamental use, under Part C of Directive 2001/18/EC from Florigene
Figure 2. - Neobythites bimarginatus. Pelvic-fin length and horizontal eye diameter showing negative allometric growth.
Figure 1 in Scientific Opinion on a notification (reference C/NL/09/02) for the placing on the market of the genetically modified carnation IFD-26407-2 with a modified colour, for import of cut flowers for ornamental use, under Part C of Directive 2001/18/EC from Florigene
Figure 1. - Neobythites bimarginatus Fourmanoir & Rivaton, 1979. SAIAB 189024, SL 122 mm. From off Madagascar (photo M. Krag, ZMUC).
Figure 6 in Human induced trauma and directed take inhibits sea turtle recovery in the Commonwealth of the Northern Mariana Islands
Figure 6. Locations of opportunistic sea turtle stranding recoveries on Tinian, CNMI from July 2009 to July 2016.
Figure 4 in Human induced trauma and directed take inhibits sea turtle recovery in the Commonwealth of the Northern Mariana Islands
Figure 4. Examples of trauma, predation, impact, and entanglement in CNMI: A) butchered green turtle carapace and head; B) spear piercing neck of live juvenile green turtle; C) three-prong spear impact to cranium; D) large stainless steel hook embedded in ventral neck; E) rubber (inner tube) straps binding front flippers; F) nesting female immobilized by flipping onto carapace; G) hatchling retained as pet; H) shark predation; I) marine debris entanglement (note marked disfigurement due to debris); and J) boat strike (photo depicts carapace repair-arrow). Photos taken under USFWS recovery permit no. TE017352-17.
Figure 5 in Human induced trauma and directed take inhibits sea turtle recovery in the Commonwealth of the Northern Mariana Islands
Figure 5. Locations of sea turtle stranding recoveries on Saipan, CNMI from April 2005 to September 2016.
Figure 3 in Human induced trauma and directed take inhibits sea turtle recovery in the Commonwealth of the Northern Mariana Islands
Figure 3. Primary causes of injury and mortality of dead and live stranded sea turtles in Saipan and Tinian from 2005-2016 (n = 89). Trauma includes butchery, spear/bullet damage, rubber inner tube binding & improper husbandry. Nutritional refers to emaciation, predation is from sharks, entanglement sources include marine debris, lines and nets. Infectious damage is evidenced by inflammation.
Figure 1 in Human induced trauma and directed take inhibits sea turtle recovery in the Commonwealth of the Northern Mariana Islands
Figure 1. Map of the Mariana Islands Archipelago showing the study site locations (denoted by stars) of the islands of Saipan and Tinian, CNMI.
The optical absorption in semiconductor to semimetal PtSe2 arises from direct transitions - Supporting data
<p>Data supporting the findings of the work:</p> <p>M. Tharrault, S. Ayari, M. Arfaoui, E. Desgué, R. Le Goff, P. Morfin, J. Palomo, M. Rosticher, S. Jaziri, B. Plaçais, P. Legagneux, F. Carosella, C. Voisin, R. Ferreira and E. Baudin, <strong>The optical absorption in semiconductor to semimetal PtSe2 arises from direct transitions</strong><em>, <a href="https://doi.org/10.48550/arXiv.2311.01847">arXiv:2311.01847 [cond-mat.mtrl-sci]</a></em>.</p> <p> </p> <p>The sample names in this study match those used in the <strong>Raman spectroscopy focused study</strong> <a href="https://doi.org/10.1088/2053-1583/ad1e79">https://doi.org/10.1088/2053-1583/ad1e79</a>. Data from that study can be accessed at <a href="https://doi.org/10.5281/zenodo.8256907">https://doi.org/10.5281/zenodo.8256907</a>.</p> <p>See the Supplemental Material for extra details.</p> <p> </p> <p>Files available:</p> <p><strong>Optical absorption spectroscopy.zip:</strong> reflectance, transmittance, real and imaginary 2D optical conductivity for exfoliated and MBE samples.</p> <p><strong>Differential reflectance with temperature.zip:</strong> differential reflectance Delta R / R pour 4 exfoliated thin samples and temperatures from 290K to 440K.</p> <p><strong>Layers label attribution.txt:</strong> number of layers for each sample.</p> <p><strong>Selected samples fig1.txt: </strong>list of samples displayed in the figure 1 of the publication.</p> <p><strong>Band diagrams.zip:</strong> Band diagrams for GGA-computed 1-12L and AB stacked bilayers as well as GW and HSE06 computed 1L and the k-points path used for the diagrams.</p> <p><strong>Optical conductivity DFT.zip:</strong> real 2D optical conductivity and jDOS computed using GGA-IPA for 1-12L and AB stacked bilayers.</p> <p><strong>Optical absorption 1L different models.csv:</strong> GGA-IPA, GW-IPA, GW-BSE and HSE06-IPA real 2D optical conductivities for the monolayer.</p> <p><strong>1L optical absorption with temperature DFT.csv</strong>: 2D real optical conductivity of 1L PtSe2 computed with EPW/ZG Quantum Espresso package for T = 0 K to 450 K.</p> <p><strong>1L electronic spectral function with temperature.zip:</strong> electronic spectral function for 1L PtSe2 for T = 0, 300 and 450 K.</p> <p><strong>Atomic orbitals decomposition.zip:</strong> band diagrams and the corresponding orbital components, as displayed in Supplemental Material.</p> <p><strong>Electronic bandgap correction.txt:</strong> GGA computed bandgaps and corrected by the energy shift.</p>
FIGURE 2 in First direct archosauromorph remains from the Early-Middle Triassic transition of the Iberian Peninsula
FIGURE 2. Geological map and stratigraphic profile of the Port del Cantó locality where IPS-73757 and IPS-90188 were collected.
FIGURE 1 in First direct archosauromorph remains from the Early-Middle Triassic transition of the Iberian Peninsula
FIGURE 1. Map of Catalonia showing the geographic occurrence of the archosauromorph teeth described here. Dashed lines indicate the boundary of each mountain range.
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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.