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Figure 1 in A Damage-Limiting Method for Extracting Bark and Ambrosia Beetles (Coleoptera: Curculionidae: Scolytinae) from Their Tunnels in Host Plants of Conservation Concern
Figure 1. Use of sticky cockroach traps to extract the Hawaiian endemic bark beetle Xyleborus mauiensis Perkins, 1900, from a Hawaiian endemic olapa (Cheirodendron trigynum) tree on the island of Lanai. a: Section of sticky trap ready for action; note the glue pushed to one side of the strip to form a globule; b: Beetle stuck to the glue and extracted from the wood.
Fig. 2 in Insecticidal activity of three plant extracts against adult Ips typograpgus L. under laboratory conditions
Fig. 2. Concentration–mortality response curves from the probit analyses testing insecticide effects of plant extracts against adults ofIps typographus in laboratory bioassays.
Fig. 1 in Insecticidal activity of three plant extracts against adult Ips typograpgus L. under laboratory conditions
Fig. 1. Mean cumulative mortality* of Ips typographus adults four days after treatments with different concentrations of three plant extracts in laboratory bioassays. The error bars represent the standard errors of means. (*corrected for a natural mortality in the control)
Fig. 3 in Insecticidal activity of three plant extracts against adult Ips typograpgus L. under laboratory conditions
Fig. 3. Kaplan-Meier estimates of the survival curves for Ips typographus adults treated with the plant extracts (2.5%) in laboratory bioassays.
Figure 1. DNA extraction with two different protocols from different noninvasive samples. Lines 1, 3, 5 in Evaluation of methods for molecular sex-typing of three heron species from different DNA sources
Figure 1. DNA extraction with two different protocols from different noninvasive samples. Lines 1, 3, 5, and 7: DNA extraction with commercial kit; Lines 2, 4, 6, and 8: DNA extracted with modified standard protocol. Lines 1–2: eggshells (Grey Heron); lines 3–4: eggshell swabs (Grey Heron); lines 5–6: pin feathers (Purple Heron); lines 7–8: contour feathers (Great Egret); 9: negative control; M: molecular marker.
Figure 5 in Ecotoxicological investigation of cyanobacterial crude extracts to Daphnia magna under subchronic test conditions
Figure 5. Filtration (A) and ingestion (B) rates of Daphnia magna after exposing to cyanobacterial crude extracts. Asterisks indicate significant differences by the Kruskal-Wallis test, followed by the Wilcoxon rank-sum test for multiple comparison (*P ≤.05).
Figure 2 in Ecotoxicological investigation of cyanobacterial crude extracts to Daphnia magna under subchronic test conditions
Figure 2. The degradation of eggs and neonates (red arrows) of the Daphnia magna gravid females exposed to cyanobacterial crude extracts. A: dead eggs, B: dead neonate, C: malformation of the tail, and D: normal tail of control Daphnia magna.
Figure 1 in Ecotoxicological investigation of cyanobacterial crude extracts to Daphnia magna under subchronic test conditions
Figure 1. The effects of cyanobacterial crude extracts on the brood size. A: the first brood, B: the second brood. Asterisks indicate significant differences by the Kruskal-Wallis test, followed by the Wilcoxon rank-sum test for multiple comparison (*P <.05, **P <.01, ***P <.001).
Figure 3 in Ecotoxicological investigation of cyanobacterial crude extracts to Daphnia magna under subchronic test conditions
Figure 3. Regression equations and correlation coefficients (R2) describing the highest correlations between the number of neonates per female (as mean) and CCE concentrations. The red color indicates the microcystin-containing crude extract and the green color indicates the microcystin-free crude extract.
Figure 4 in Ecotoxicological investigation of cyanobacterial crude extracts to Daphnia magna under subchronic test conditions
Figure 4. The effects of cyanobacterial crude extracts on somatic growth of Daphnia magna. Asterisks indicate significant differences by the Kruskal-Wallis test, followed by the Wilcoxon rank-sum test for multiple comparison (*P <.05, **P <.01, ***P <.001).
Figure 2 in Larvicidal, and cytoxicity of Lepidium sativum L. seed extract against Culex pipiens L. (Diptera: Culicidae)
Figure 2. Percentage hatchability and activity of the ethyl acetate extract of Lepidium sativum against Culex pipiens third instar larvae treated with different concentrations. Significant differences were assessed using one-way ANOVA followed by Tukey's test, with p <0.05 considered to indicate significant differences. Different letters indicate significant differences.
Figure 4 in Larvicidal, and cytoxicity of Lepidium sativum L. seed extract against Culex pipiens L. (Diptera: Culicidae)
Figure 4. Effect of ethyl acetate extract of L. sativum on the morphology of human umbilical vein endothelial cells. The morphological and nuclear features were observed after 24 h incubation and imaged under an inverted microscope (200× magnification). The arrows point to the fragmented DNA.
Figure 1 in Compatibility of entomopathogenic nematodes with plant extracts and post-exposure virulence test under laboratory condition
Figure 1. Percentage survival of the EPN Species in aqueous and ethanol extracts of A. amatymbica and E. elephantina after 72 h exposure. Different lower-case characters represent significant differences at p <0.05.
Figure 3 in Larvicidal, and cytoxicity of Lepidium sativum L. seed extract against Culex pipiens L. (Diptera: Culicidae)
Figure 3. Photomicrographs of midguts of Cx. pipiens larvae demonstrating: (Chouin-Carneiro et al., 2016). Longitudinal sections in the midguts (MG) of control larvae with normal and healthy epithelial cells (Ec), microvilli (Mv), nuclei (n), and regenerative cells (Rc). Notice absence of the lesions. H&E stain. (C-D): Longitudinal sections in midguts of AzE-treated larvae, with blebbing (Bc) and protruding (Pc) of the epithelial cells into the lumen (Lu) of midgut of the larvae and degraded microvilli (DMv). H&E stain.
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. 1 in The effects of non-host plant extracts on the oviposition deterrent and ovicidal activity of Conopomorpha sinensis Bradley (Lepidoptera: Gracillariidae)
Fig. 1. The effect of 5 plant extracts on oviposition activity index (OAI) values of Conopomorpha sinensis in the choice test. Plant extracts with oviposition activity indexes of ≥ 0.3 are considered as attractants, whereas those of ≤ −0.3 are considered to be deterrents. Negative values indicate that more eggs were deposited in the control group than those in groups receiving treatment with plant extracts.
Fig. 3. Energy dispersive x in Extraction and elemental composition of meconium in Polistes dominulus (Hymenoptera: Vespidae)
Fig. 3. Energy dispersive x-ray spectra of Polistes dominulus meconia samples according to locality number: (1) Hatay, Payas; (2) Hatay, Erzin, YeŞiltepe; (3) İÇel, Mezitli; (4) İÇel, Tarsus, Kaleburcu; (5) İÇel, Tarsus, Çamtepe; (6) Osmaniye, Kadirli; (7) Osmaniye, Toprakkale; (8) Adana, Yüreğir; (9) Adana, SarıÇam; (10) Adana, Kozan, Anavarza; (11) Adana, Ceyhan; (12) Adana, İmamoglu.
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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.