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288 results for “corn”

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Figure 4 in Does narrow row spacing suppress weeds and increase yields in corn and soybean? A meta-analysis

Figure 4. The effect of narrow row spacing (<76 cm) on (A) weed density, (B) weed biomass, (C) weed control, and (D) weed seed production as explained by the subgroups of crop,tillage,weed type,weed management method, herbicide application frequency, and time. The vertical black dashed line indicates zero effect.The black dots represent mean effect sizes (log of response ratios [lnðRRÞ]) for each subgroup, and the black lines represent their respective 99% confidence intervals (CIs). The numbers in parentheses indicate the number of observations followed by the number of studies for each effect size. The effect sizes were considered significantly different when their 99% CIs did not overlap or contain zero.

opencc-by-4.0Sep 2023View details →
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Figure 7 in Does narrow row spacing suppress weeds and increase yields in corn and soybean? A meta-analysis

Figure 7. Density plots show the distribution of individual effect sizes (log of response ratios [ln(RR)]) of weed density,biomass,control, weed seed production, and crop yield.

opencc-by-4.0Sep 2023View details →
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Figure 1 in Microorganisms from corn stigma with biocontrol potential of Fusarium verticillioides

Figure 1. Percentage of mycelial growth inhibition of Fusarium verticillioides by endophytic and epiphytic microorganisms from maize silks collected in different Brazilian regions.

opencc-by-4.0Dec 2022View details →
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Fig. 2 in Genetically modified maize resistant to corn earworm (Lepidoptera: Noctuidae) in Sinaloa, Mexico

Fig. 2. Percentage of corn ears ear damaged by Helicoverpa zea in Agrisure® VipteraTM 3111, AgrisureTM 3000 GT, and their respective isolines at El Dorado, Culiacan, and Navolato (Sinaloa, Mexico). 2012. Genetically modified hybrids and their respective isolines followed by the same letter do not differ significantly (LSD; P> 0.05). ic = insecticide control

opencc-by-4.0Sep 2015View details →
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Fig. 1 in Genetically modified maize resistant to corn earworm (Lepidoptera: Noctuidae) in Sinaloa, Mexico

Fig. 1. Percentage of corn ears damaged by Helicoverpa zea in AgrisureTM 3000 GT, Agrisure® VipteraTM 3110, and their respective isolines at Oso Viejo, Culiacan (Sinaloa, Mexico) during 2011.Genetically modified hybrids and their respective isolines followed by the same letter do not differ significantly (LSD; P> 0.05). ic = insecticide control.

opencc-by-4.0Sep 2015View details →
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Datasets: Laser scarecrows reduce avian corn-foraging propensity but not bout length in aviary trials

<p>This archive is comprised of 3 files:</p> <p>(1) Archive Metadata: a description of the data collection, behavioral sampling, and datafile structure (variables);</p> <p>(2) An excel file containing scan sample data used in 2 analyses; and&nbsp;</p> <p>(3) An excel file containing focal foraging bout data for a 3rd analysis for the named manuscript.</p>

opencc-by-4.0Jul 2024View details →
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Raw data for: Spatial and temporal variation in farmland bird nesting ecology: Implications for effective Corn Bunting Emberiza calandra conservation

<p>These are raw data accompanying the study "<span>Spatial and temporal variation in farmland bird nesting ecology: Implications for effective Corn Bunting Emberiza calandra conservation</span>". All information on data origin, data analysis, and derived implications will be available with the original publiation.</p>

opencc-by-4.0Jul 2024View details →
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Fig. 3 in Seasonal and vertical distribution of Dalbulus maidis (Hemiptera: Cicadellidae) in Brazilian corn fields

Fig. 3. Abundance of Dalbulus maidis from yellow sticky card and yellow pan traps positioned at 2 heights in corn grown during (a, c) the rainy season and (b, d) the dry season.

opencc-by-4.0Dec 2016View details →
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Fig. 1 in Seasonal and vertical distribution of Dalbulus maidis (Hemiptera: Cicadellidae) in Brazilian corn fields

Fig. 1. Trends in capture of Dalbulus maidis, and weather variables, during the study at Teresina, Piauí, Brazil, in 2013.

opencc-by-4.0Dec 2016View details →
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Fig. 2 in Seasonal and vertical distribution of Dalbulus maidis (Hemiptera: Cicadellidae) in Brazilian corn fields

Fig. 2. Quality of fit of generalized linear mixed models used to assess the effect of trap type on capture of D. maidis at 2 heights, expressed as the ratio of values observed to values predicted by the models. Type 1 = yellow sticky card and type 2 = yellow water pan. (a) Rainy season. (b) Dry season.

opencc-by-4.0Dec 2016View details →
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Figure 3 in Insecticidal effect of diatomaceous earth and dolomite powder against Corn weevil Sitophilus zeamais Motschulsky, 1855 (Coleoptera: Curculionidae)

Figure 3. Pictures of Sitophilus zeamais control taken by scanning electron microscopy (SEM). A. Dorsal view: trichoid sensilla (Se), sensilla (S), antenna (A), rostrum (R), elytrum (E). Bar = 500 µm. B. Rostrum and antenna: trichoid sensilla (Se), sensilla (S). Bar = 100 µm. C. Antenna: trichoid sensilla (Se). Bar = 20 µm. D. Elytrum: sensilla (S), suture (Su). Bar = 20 µm. E. Elytrum: sensilla (S), suture (Su). Bar = 50 µm. F. Abdomen, ventral view: sensilla (S). Bar = 10 µm.

opencc-by-4.0Oct 2020View details →
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Figure 2 in Insecticidal effect of diatomaceous earth and dolomite powder against Corn weevil Sitophilus zeamais Motschulsky, 1855 (Coleoptera: Curculionidae)

Figure 2. Mortality at different concentrations (mg) of diatomaceous earth and dolomite powder used for control of Sitophilus zeamais Motschulsky, 1855 (Coleoptera: Curculionidae), after different exposure times. DE:Diatomaceous earth and DOL: Dolomite powder.

opencc-by-4.0Oct 2020View details →
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Figure 5 in Insecticidal effect of diatomaceous earth and dolomite powder against Corn weevil Sitophilus zeamais Motschulsky, 1855 (Coleoptera: Curculionidae)

Figure 5. Pictures of Sitophilus zeamais exposed to inert dusts taken by scanning electron microscopy (SEM). A. Elytrum (E) of insect exposed to diatomaceous earth: sensilla (S), suture (Su). Bar = 200 µm. B. Elytrum (E) of insect exposed to dolomite powder: sensilla (S), suture (Su). Barra = 20 µm. C. Leg of insect exposed to dolomite powder: sensilla (S). Bar = 100 µm. D. Claw of insect exposed to dolomite powder. Bar = 50 µm.

opencc-by-4.0Oct 2020View details →
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Figure 7 in Assessment of entomopathogenic nematodes and their symbiotic bacteria to control the stink bugs Euschistus heros and Dichelops melacanthus (Heteroptera: Pentatomidae) in the soybean-corn succession system

Figure 7. Corrected mortality (%) of Euschistus heros and Dichelops melacanthus (Abbott's formula) seven days after their exposition to Steinernema diaprepesi AM163 applied on a double layer straw-over-sand substrate, at the rate of 88.4 IJs/cm² (1000 IJs/insect) (**p &lt;0.01; Student's t test).

opencc-by-4.0Jun 2021View details →
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Figure 8 in Assessment of entomopathogenic nematodes and their symbiotic bacteria to control the stink bugs Euschistus heros and Dichelops melacanthus (Heteroptera: Pentatomidae) in the soybean-corn succession system

Figure 8. Corrected mortality (%) of Dichelops melacanthus (Abbott's formula) seven days after its exposition to Steinernema diaprepesi AM163 and Steinernema carpocapsae IP1 applied on a double layer straw-over-sand substrate, at the rate of 88.4 IJs/cm² (1000 IJs/insect) (p&gt; 0.05; Student's t test).

opencc-by-4.0Jun 2021View details →
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Figure 9 in Assessment of entomopathogenic nematodes and their symbiotic bacteria to control the stink bugs Euschistus heros and Dichelops melacanthus (Heteroptera: Pentatomidae) in the soybean-corn succession system

Figure 9. Mortality of Euschistus heros adults seven days after their exposition to the nematode Steinernema diaprepesi AM163 applied on the straw at the rate of 88.4 IJs/cm² (1000 IJs/insect), inside greenhouse (**p &lt;0.01; Student's t test).

opencc-by-4.0Jun 2021View details →
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Figure 6 in Assessment of entomopathogenic nematodes and their symbiotic bacteria to control the stink bugs Euschistus heros and Dichelops melacanthus (Heteroptera: Pentatomidae) in the soybean-corn succession system

Figure 6. Corrected mortality (%) of Euschistus heros adults (Abbott formula) seven days after their exposition to Steinernema diaprepesi AM163 applied on two substrates with two-layer thicknesses, at the rate of 88.4 IJs/cm² (1000 IJs/insect). Averages followed by the same letter in the column do not differ significantly according to the Tukey test 5%.

opencc-by-4.0Jun 2021View details →
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Figure 3 in Assessment of entomopathogenic nematodes and their symbiotic bacteria to control the stink bugs Euschistus heros and Dichelops melacanthus (Heteroptera: Pentatomidae) in the soybean-corn succession system

Figure 3. Mortality (%) of Euschistus heros adults 7 days after their inoculation with symbiotic bacteria cultures. Xn.: Xenorhabdus. Ph.: Photorhabdus. Averages followed by the same letter do not differ significantly according to the Tukey test 5%.

opencc-by-4.0Jun 2021View details →
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Figure 5 in Assessment of entomopathogenic nematodes and their symbiotic bacteria to control the stink bugs Euschistus heros and Dichelops melacanthus (Heteroptera: Pentatomidae) in the soybean-corn succession system

Figure 5. Reproduction of Steinernema diaprepesi AM163 in Euschistus heros exposed to different rates of the nematode. Averages followed by the same letter do not differ significantly according to the Tukey test 5%.

opencc-by-4.0Jun 2021View details →
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Figure 1 in Assessment of entomopathogenic nematodes and their symbiotic bacteria to control the stink bugs Euschistus heros and Dichelops melacanthus (Heteroptera: Pentatomidae) in the soybean-corn succession system

Figure 1. Mortality (%) of Euschistus heros seven days after their exposition to 16 EPNs strains applied on sand substrate, at the rate of 140 IJs/cm² (1000 IJs/insect). Sn.: Steinernema. Ht.: Heterorhabditis. Averages followed by the same letter do not differ significantly according to the Tukey test 5%.

opencc-by-4.0Jun 2021View details →

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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record