Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
302
datasets available to search
ShareScore release 0.9.0
Dataset results
302 results for “entomopathogen”
Figure 7 in Indiscriminate ingestion of entomopathogenic nematodes and their symbiotic bacteria by Aedes aegypti larvae: a novel strategy to control the vector of Chikungunya, dengue and yellow fever
Figure 7. Aedes aegypti larval mortality when exposed to supernatants and cell suspensions of Xenorhabdus nematophila (X. n.) and Photorhabdus laumondii (P. l.) in 24 well plates. Different uppercase or lower letters above error bars indicate statistical significance (Tukey's test p ≤ 0.05).
Figure 3 in Indiscriminate ingestion of entomopathogenic nematodes and their symbiotic bacteria by Aedes aegypti larvae: a novel strategy to control the vector of Chikungunya, dengue and yellow fever
Figure 3. Different stages of Heterorhabditis bacteriophora colonization of Aedes aegypti larvae (3rd instar). H. bacteriophora within larvae at 2-day post inoculation (a), H. bacteriophora emerging out of larvae upon larval dissection at 7-day post inoculation) (b), adult H. bacteriophora within larvae along with large number of infective juveniles (IJs) released from another adult H. bacteriophora (c). Black arrows indicate adult H. bacteriophora, whereas green arrows indicate newly emerged IJs.
Figure 7 in Basic laboratory and field manual for conducting research with the entomopathogenic nematodes, Steinernema and Heterorhabditis, and their bacterial symbionts
Figure 7. Scanning electron microscopy images of Steinernema beitlechemi infective juvenile and female. A–D: Infective juvenile. A: Head region with four papillae, amphid openings (a) and excretory pore (ep); B: Lateral field in mid-body (ridges numbered 1–6); C: Lateral field in tail region with anus and phasmid opening (arrow); D: Tail region with anus and phasmid openings (arrows), ventral view. E, F: First generation female. E: Vulva; F: Tail with mucron (m), ventro-lateral.
Figure 6 in Basic laboratory and field manual for conducting research with the entomopathogenic nematodes, Steinernema and Heterorhabditis, and their bacterial symbionts
Figure 6. Storage of entomopathogenic nematodes in clear tissue culture flasks on the left and Tetrapak containers on the right.
Figure 3 in Basic laboratory and field manual for conducting research with the entomopathogenic nematodes, Steinernema and Heterorhabditis, and their bacterial symbionts
Figure 3. White trap system with entomopathogenic nematode-infected Galleria mellonella and Tenebrio molitor cadavers. Color change of infected cadavers is observed a few days after death. Heterorhabdid- infected cadaver generally turns red (A and C); steinernematids- infected are brown, tan or even black (C and D).
Figure 4 in New insights on the impact of earthworm extract on the growth of beneficial soil fungi: species-specific alteration of the nematophagous fungal growth and limitation of an entomopathogenic fungus
Figure 4. Growth of Purpureocillium lilacinum after 20 days postexposer to two different earthworm based media: fresh earthworms (FE) (four concentration C1, C2, C3, and C4), and earthworms devoid of gut contents (EDG) (four concentration C1, C2, C3, and C4), C1 = 40 g/L, C2 = 20 g/L, C3 = 10 g/L, C4 = 5 g/L, and two rich media: potato dextrose agar (PDA), and brain heart infusion (BHI).
Figure 5 in New insights on the impact of earthworm extract on the growth of beneficial soil fungi: species-specific alteration of the nematophagous fungal growth and limitation of an entomopathogenic fungus
Figure 5. Evaluation of conidial germination of the fungus Beauveria bassiana exposed to two different earthworm extracts: fresh earthworms (FE) and earthworms without gut contents, EDG, and two conventional media: potato dextrose agar (PDA), and brain heart infusion agar (BHI). A. Percentage germination on conventional and earthworm-based media. B. Percent germination as a function of concentration and earthworm-based medium. Concentrations are equivalent to C1 = 40 g/L, C2 = 20 g/L, C3 = 10 g/L, and C4 = 5 g/L. Results of one-way ANOVA (A) or two-way ANOVA (B), and differences are significant according to Tukey's test (HSD) and groups "a", "b" and "c".
Figure 3 in New insights on the impact of earthworm extract on the growth of beneficial soil fungi: species-specific alteration of the nematophagous fungal growth and limitation of an entomopathogenic fungus
Figure 3. Evaluation of vegetative growth, conidial production and germination in the fungus Purpureocillium lilacinum exposed to two earthworm extracts: fresh earthworm (FE), earthworms devoid of intestinal contents (EDG) and two conventional media: potato dextrose agar (PDA), and brain heart infusion agar (BHI). A. Cumulative growth from 3 to 18 days according to conventional and earthworm-based media. B. Cumulative growth as a function of concentration and earthworm-based medium. C. Conidia production (×10⁵ conidia/mL) according to conventional and earthworm-based media. D. Conidia production (×10⁵ conidia/mL) according to concentration and earthworm-based medium. E. Percent germination on conventional and earthworm-based media. F. Percent germination as a function of concentration and earthworm-based medium. Concentrations are equivalent to C1 = 40 g/L, C2 = 20 g/L, C3 = 10 g/L, and C4 = 5 g/L. Results of one-way ANOVA (A, C, E) or two-way ANOVA (B, D, F), and differences are significant at Tukey's test (HSD) and groups "a", "b" and "c".
Figure 1 in New insights on the impact of earthworm extract on the growth of beneficial soil fungi: species-specific alteration of the nematophagous fungal growth and limitation of an entomopathogenic fungus
Figure 1. Evaluation of vegetative growth, conidial production and germination in the fungus Arthrobotris musiformis exposed to two earthworms' extracts: fresh earthworm (FE), earthworms devoid of intestinal contents (EDG) and two conventional media: potato dextrose agar (PDA), and brain heart infusion agar (BHI). A. Cumulative growth from 3 to 18 days according to conventional and earthworm-based media. B. Cumulative growth as a function of concentration and earthworm-based medium. C. Conidia production (×10⁵ conidia/mL) according to conventional and earthworm-based media. D. Conidia production (×10⁵ conidia/mL) according to concentration and earthworm-based medium. E. Percent germination on conventional and earthworm-based media. F. Percent germination as a function of concentration and earthworm-based medium. Concentrations are equivalent to C1 = 40 g/L, C2 = 20 g/L, C3 = 10 g/L, and C4 = 5 g/L. Results of one-way ANOVA (A, C, E) or two-way ANOVA (B, D, F), and differences are significant at Tukey's test (HSD) and groups "a", "b" and "c".
Fig. 2 in A new methodology to evaluate entomopathogenic fungi and formulated insecticides to control adults of Aedes aegypti (Diptera: Culicidae)
Fig. 2. The mortality proportion of Aedes aegypti females caused by isolates of Beauveria spp. at 20 d afer application. Error bars represent 95% confidence intervals back-transformed from the logistic scale. An asterisk (*) indicates that the treatment was significantly different from the control.
Fig. 1 in A new methodology to evaluate entomopathogenic fungi and formulated insecticides to control adults of Aedes aegypti (Diptera: Culicidae)
Fig. 1. Adults of Aedes aegypti L. contained inside a Petri dish covered with tulle: (a) Petri dish; (b) tulle; (c) straw; (d) natural rubber band.
Fig. 2. Adult spotted wing drosophila emergence from berries 2 in Efficacy of entomopathogenic fungal products for biological control of spotted wing drosophila (Diptera: Drosophilidae) under laboratory conditions
Fig. 2. Adult spotted wing drosophila emergence from berries 2 wk afer re- moval from the arenas. Bars with the same letter are not significantly different from each other (P> 0.05). Error bars represent standard error of the mean.
Fig. 1 in Efficacy of entomopathogenic fungal products for biological control of spotted wing drosophila (Diptera: Drosophilidae) under laboratory conditions
Fig. 1. Percent mortality of spotted wing drosophila afer 24, 48, 72, and 168 h in each treatment (Untrt = deionized water treated control, BotL = BotaniGard low rate, BotH = BotaniGard high rate, PFRL = PFR 97 low rate, and PFRH = PFR 97 high rate). Bars with the same letter are not significantly different from each other (P> 0.05). N. S. = no significant differences (P> 0.05). Error bars represent standard error of the mean.
Fig. 2 in Evaluation of isolates of entomopathogenic fungi in the genera Metarhizium, Beauveria, and Isaria, and their virulence to Thaumastocoris peregrinus (Hemiptera: Thaumastocoridae)
Fig. 2. Daily mean survival curves for adult Thaumastocoris peregrinus exposed to entomopathogenic fungal isolates of the genera Beauveria, Metarhizium, and Isaria for a period of 10 d. The horizontal dotted line indicates insect mortality of 50%.
Fig. 1 in Evaluation of isolates of entomopathogenic fungi in the genera Metarhizium, Beauveria, and Isaria, and their virulence to Thaumastocoris peregrinus (Hemiptera: Thaumastocoridae)
Fig. 1. Percentage of confirmed mortality of Thaumastocoris peregrinus, treat- ed with suspensions of 1 × 108 conidia per mL of entomopathogenic fungal isolates. Different letters above the bars indicate differences between treatments by Tukey's test (P <0.05). Bars represent the error ± 1 × SEM (df = 100).
Fig. 3 in Isolation of native strains of entomopathogenic fungi from agricultural soils of northeastern Mexico and their virulence on Spodoptera exigua (Lepidoptera: Noctuidae)
Fig. 3. Changes in the metamorphosis of Spodoptera exigua caused by isolates (HEB1, HIB-12) and collection strains (GHA, Ma) of entomopathogenic fungi under laboratory conditions (26 °C, 65 ± 5% RH, 14:10 h [L:D] photoperiod). (A) HEB1 (Beauveria bassiana); (B) GHA (Beauveria bassiana); (C) HIB-12 (Metharizium anisopliae); (D) Ma (Metharizium anisopliae). Lines in the bars indicate the standard error.
Fig. 2 in Isolation of native strains of entomopathogenic fungi from agricultural soils of northeastern Mexico and their virulence on Spodoptera exigua (Lepidoptera: Noctuidae)
Fig. 2. Interruption of the metamorphosis of Spodoptera exigua caused by isolates (HEB1, HIB-12) and collection strains (GHA, Ma) of entomopathogenic fungi under laboratory conditions (26 °C, 65 ± 5% RH, 14:10 h [L:D] photoperiod). Lines in the bars indicate the standard error.
Fig. 1 in Isolation of native strains of entomopathogenic fungi from agricultural soils of northeastern Mexico and their virulence on Spodoptera exigua (Lepidoptera: Noctuidae)
Fig. 1. Phylogenetic tree reconstructed from internal transcribed spacer sequences of the isolates compared with referenced internal transcribed spacer sequences deposited in the NCBI GenBank. The phylogram size bar represents a 1% sequence divergence. Labelled branches represent referenced internal transcribed spacer sequences.
Fig. 3 in Carrier and vector of Pectobacterium carotovorum subsp. carotovorum and its handling through a base of entomopathogenic fungi in Agave sp.
Fig. 3. Massive growth of the Metarhizium anisopliae fungus on the Pectobacterium carotovora bacterium.
Fig. 2 in Carrier and vector of Pectobacterium carotovorum subsp. carotovorum and its handling through a base of entomopathogenic fungi in Agave sp.
Fig. 2. Countable growth of the Pectobacterium carotovora bacterium in a BD Bioxion cultivation medium (MacConkey agar).
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.