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14,867 results for “Determinants”
Fig. 6 in Does prior feeding behavior by previous generations of the maize weevil (Coleoptera: Curculionidae) determine future descendants feeding preference and ovipositional suitability?
Fig. 6. Number (SE) of S. zeamais male and female (n = 200) emergence when reared on the individual host grains: corn, barley, brown rice, and white rice. Means with the same letter are not significantly different.
Fig. 5 in Does prior feeding behavior by previous generations of the maize weevil (Coleoptera: Curculionidae) determine future descendants feeding preference and ovipositional suitability?
Fig. 5. Mean (SE) number of S. zeamais (n = 8,000) attracted to corn, barley, brown rice, and white rice, with a 200 µL Eppendorf tube containing the pheromone lure placed in brown rice. Means with the same letter are not significantly different.
Fig. 2 in Does prior feeding behavior by previous generations of the maize weevil (Coleoptera: Curculionidae) determine future descendants feeding preference and ovipositional suitability?
Fig. 2. Mean (SE) number of S. zeamais (n = 8,000) attracted to corn, barley, brown rice, and white rice, with a 200 µL Eppendorf tube containing the pheromone lure placed in corn. Weevils were reared on corn, barley, brown rice, and white rice, then presented with a choice of 4 host grains. Means with the same letter are not significantly different.
Fig. 1 in Does prior feeding behavior by previous generations of the maize weevil (Coleoptera: Curculionidae) determine future descendants feeding preference and ovipositional suitability?
Fig. 1. Mean (SE) number of S. zeamais (n = 8,000) attracted to corn, barley, brown rice, and white rice. Weevils were reared on corn, barley, brown rice, and white rice, then presented with a choice of 4 host grains. Means with the same letter are not significantly different.
Fig. 4 in Does prior feeding behavior by previous generations of the maize weevil (Coleoptera: Curculionidae) determine future descendants feeding preference and ovipositional suitability?
Fig. 4. Mean (SE) number of S. zeamais (n = 8,000) attracted to corn, barley, brown rice, and white rice, with a 200 µL Eppendorf tube containing the pheromone lure placed in white rice. Means with the same letter are not significantly different.
Fig. 2 in An investigation of endoparasites and the determinants of parasite infection in European hedgehogs (Erinaceus europaeus) from Denmark
Fig. 2. Overall parasite prevalence by age. Numbers on the x-axis indicate age in years. Numbers on top of the columns indicate number of individuals, in red for hedgehogs with endoparasites, in blue for hedgehogs without endoparasites. Statistically significant differences in proportions of hedgehogs with endoparasites versus without hedgehogs, were found between juveniles (<1 year) and age classes 1–6 years, and between hedgehogs of one year versus two years of age as shown in the upper right corner of the figure. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 4 in An investigation of endoparasites and the determinants of parasite infection in European hedgehogs (Erinaceus europaeus) from Denmark
Fig. 4. Overall parasite prevalence by region. Numbers indicate number of individuals, in red for hedgehogs with parasites, in blue without. JNL denotes Jutland north of the Limfjord, and JSL abbreviates Jutland south of the Limfjord. Statistically significant differences in proportions of hedgehogs with endoparasites versus hedgehogs without endoparasites were found between Zealand and Jutland south of the Limfjord (JSL), and Zealand and Falster (p <0.05 in both cases). We removed seven individuals from the analyses (Jutland north of the Limfjord (n = 1), Jutland south of the Limfjord (n = 4), Lolland (n = 1), Bornholm (n = 1)), as they were the only individuals found in April and December, and four were only categorised as collected in "Summer 2016". (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 1. A in An investigation of endoparasites and the determinants of parasite infection in European hedgehogs (Erinaceus europaeus) from Denmark
Fig. 1. A map representing Denmark and the geographical locations of the 299 dead European hedgehogs examined. Colours indicate the different species of endoparasites detected in each individual. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 2 in CCDC 204627: Experimental Crystal Structure Determination
Fig. 2. Thaumastosaurus sulcatus, partial right squamosal (lamella alaris squamosi), paratype (MSUVP 2021). Late Eocene "Rodent Bed" of the Hordle Cliff Locality, Hampshire, England. A, B. Lateral views. C. Medial view.
Fig. 1 in CCDC 204627: Experimental Crystal Structure Determination
Fig. 1. Thaumastosaurus sulcatus sp. nov., partial left maxilla, holotype (MSUVP 1976), Late Eocene "Mammal Bed", Hordle Cliff Locality, Hampshire, England. A, B. Lingual view. C. Enlarged view of tooth indicated by arrow at B. D, E. Labial views.
Fig. 2 in CCDC 651299: Experimental Crystal Structure Determination
Fig. 2. Nemestrinid fly Ahirmoneura neimengguensis Zhang, Yang, and Ren, gen. et sp. nov., holotype CNU−B−NN2006003, from the Daohugou Village, Inner Mongolia, China; Aalenian−Bajocian Jiulongshan Formation, Middle Jurassic. A. Body with wings photograph in dorsal view. B. Camera lucida drawing, based on the original photograph, in dorsal view. C. Camera lucida drawing, base of vein C details.
Fig. 1 in CCDC 651299: Experimental Crystal Structure Determination
Fig. 1. Location of the type locality of Ahirmoneura neimengguensis Zhang, Yang, and Ren, gen. et sp. nov. Daohugou Village, Shantou Township, Ningcheng County, Inner Mongolia, China. A. Outlined location. B. Detailed location. Abbreviations: Chc, Changchougou Formation; Chch, Chuanlinggou Formation; Chd, Dahongyu Formation; Cht, Tuanshanzi Formation; J2j, Jiulongshan Formation; J2t, Tiaojishan Formation; Ky, Yixian Formation; Q, Quaternary; Dms, Dalaiyingzi erosion surface; Mgn, Maanshan gneiss.
Fig. 4 in CCDC 615855: Experimental Crystal Structure Determination
Fig. 4. Distribution of Cenozoic marsupials in North−Africa and Eurasia. Peradectidae: 1, Chambi, Tunisia (early Eocene); 2, Fayum, Egypt (early Oligocene); 3, Taqah, Oman (early Oligocene); 4, Li Basin, Thailand (middle Miocene); 5, Sonlinzhuang, China (early Miocene). Herpetotheriidae: 6, Zaissan Basin, Kazakhstan (late Eocene – early Oligocene); 7, Vastan lignite mine, India (early Eocene); 8, Bugti Hills, Pakistan (early Oligocene); 9, Shanghuang fissure fillings B and C, Jiangsu, China (middle Eocene). Localities that yielded remains of disputable marsupial affinity (see text): 7, Vastan lignite mine, India (early Eocene); 10, Kartal Formation, Turkey (Eocene).
Fig. 1 in CCDC 615855: Experimental Crystal Structure Determination
Fig. 1. Geographic location of the marsupial−bearing locality of Paali Nala−DBC2 (denoted by an asterisk), the lowermost part of the Chitarwata Formation (Bugti Member, Oligocene), in the Bugti Hills (Central Pakistan, eastern Balochistan).
Fig. 2 in CCDC 615855: Experimental Crystal Structure Determination
Fig. 2. Asiadidelphis akbarbugtii sp. nov. from Paali Nala−DBC2 (Bugti Hills, Balochistan, Pakistan). A. Holotype PMNH−DBC2−2180, left M2 in labial (A1), occlusal (A2), and mesial (A3) views. B. PMNH−DBC2−2179, left M2 in labial (B1), occlusal (B2), and mesial (B3) views. C. PMNHDBC2−2223, right M4 in occlusal view. Original drawings by Laurence Meslin, copyright CNRS−Meslin.
Fig. 3 in CCDC 615855: Experimental Crystal Structure Determination
Fig. 3. Asiadidelphis akbarbugtii sp. nov. from Paali Nala−DBC2 (Bugti Hills, Balochistan, Pakistan). A. PMNH−DBC2−2179, left M2 in occlusal view. B. PMNH−DBC2−2180 (holotype), left M2 in occlusal view. Stereo pairs.
D-PLACE dataset derived from Kreft and Jetz 2007 'Global patterns and determinants of vascular plant diversity'
<p>Cite the source of the dataset as:</p> <blockquote> <p>Kreft H, Jetz W. Global patterns and determinants of vascular plant diversity. Proc Natl Acad Sci. 2007;104: 5925–5930.</p> </blockquote>
FIGURE 1 in Taxonomic and functional turnover of Amazonian stream fish assemblages is determined by deforestation history and environmental variables at multiple scales
FIGURE 1 | Sampled sites and forest fragments in the Machado River basin, Brazil. The inset map of Brazil depicts the relative location of the study area (black) within the Madeira River basin (dark gray), inside the Amazon biome (light gray).
FIGURE 4 in Taxonomic and functional turnover of Amazonian stream fish assemblages is determined by deforestation history and environmental variables at multiple scales
FIGURE 4 | Explained variation of environmental contribution in turnover metrics partitioned by MRM and associated commonality analysis into pure local, shared and pure catchment components. RC = Raup-Crick; MPD = mean pairwise distance; MNTD = mean nearest taxon distance; all = all sampled streams; ref = streams with forested watersheds; new = streams with recently deforested watersheds; old = streams with historically deforested watersheds.
FIGURE 2 in Taxonomic and functional turnover of Amazonian stream fish assemblages is determined by deforestation history and environmental variables at multiple scales
FIGURE 2 | Distribution of sampling sites with (A) forest patches ranked according to the forest quality multimetric index and (B) effective forest cover. Non-forested area is white and is not included in the multimetric index calculation (or legend).
ScienceDex guides
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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.