Find research datasets worth reusing

opencc-by-4.0Jun 2016View details →

Fig. 2 in Inherited sterility in Tuta absoluta (Lepidoptera: Gelechiidae): Pest population suppression and potential for combined use with a generalist predator

Fig. 2. Population suppression by irradiated individuals and their progeny over 12 weeks at a 15:1 irradiated:untreated ratio. a) Number of eggs/cage, b) number of small larvae /cage and c) number of large larvae/cage (mean ± SE). Only 1 release of irradiated moths was made, i.e., at the beginning of the experiment. For details see text on Experiment 2.

opencc-by-4.0Sep 2016View details →

Fig. 1 in Efficacy of five insecticides targeting spring and fall populations of sugarcane beetle adults

Fig. 1. Adjusted percentage of mortality of fall and spring populations of sugarcane beetles by active ingredient at low label rate. Treatment means with different upper case letters are significantly different (P ≤ 0.05; ANOVA and LSD test) for the fall population. Treatment means with different lower case letters are significantly different (P ≤ 0.05; ANOVA and LSD test) for the spring population.

Fig. 7 in Population genetics of Oligonychus perseae (Acari: Tetranychidae) collected from avocados in Mexico and California

Fig. 7. Local aerial dispersal behavior detected in field populations of Oligonychus perseae. A. Cultivar 'Hass' avocado tree foliage from a commercial orchard in California infested with O. perseae as indicated by characteristic necrotic spots on the leaf undersurface. B. Adult O. perseae being carried by wind currents land on hand and clothes during assessment of mite infestation. C. A group of O. perseae adults (individual mites within black dashed circles) begins to disperse on a fine silk strand from a cultivar 'Hass' avocado leaf. All photographs by JRL.

opencc-by-4.0Sep 2016View details →

Fig. 2 in Efficacy of five insecticides targeting spring and fall populations of sugarcane beetle adults

Fig. 2. Adjusted percentage of mortality of spring sugarcane beetles by active ingredient at both low and high label rate. Treatment means with different upper case letters are significantly different (P ≤ 0.05; ANOVA and LSD test) at the low rate. Treatment means with different lower case letters are significantly different (P ≤ 0.05; ANOVA and LSD test) at the high rate.

Fig. 5. Sequence variation among 4 28S in Population genetics of Oligonychus perseae (Acari: Tetranychidae) collected from avocados in Mexico and California

Fig. 5. Sequence variation among 4 28S genotypes identified from Oligonychus perseae populations in California, Mexico, and Costa Rica. Genotypes are named according to 3 genetic clusters identified from cytochrome oxidase subunit 1 (COI) haplotypes (see Fig. 2).

Fig. 6 in Population genetics of Oligonychus perseae (Acari: Tetranychidae) collected from avocados in Mexico and California

Fig. 6. Divergence in the 28S rRNA region among Oligonychus perseae specimens with deeply diverged mitochondrial haplotypes (see Fig. 2). Neighborjoining tree constructed in MEGA version 6.06. Tree is drawn to scale and branch lengths represent number of base differences per site (p-distance). Bootstrap (1,000 replicates) support shown for major branches.

Fig. 3. Sequence variation among 4 internal transcribed spacer 2 in Population genetics of Oligonychus perseae (Acari: Tetranychidae) collected from avocados in Mexico and California

Fig. 3. Sequence variation among 4 internal transcribed spacer 2 (ITS2) genotypes identified from Oligonychus perseae populations in California,Mexico, and Costa Rica. Genotypes are named according to 3 genetic clusters identified from cytochrome oxidase subunit 1 (COI) haplotypes (see Fig. 2).

Fig. 4 in Population genetics of Oligonychus perseae (Acari: Tetranychidae) collected from avocados in Mexico and California

Fig. 4. Divergence in the internal transcribed spacer 2 (ITS2) rRNA region among Oligonychus perseae specimens with deeply diverged mitochondrial haplotypes (see Fig. 2). Additional sequences from Ben-David et al. (2007), Guzmán-Valencia et al. (2014), and Perez-Sayas et al. (unpublished). Neighborjoining tree constructed in MEGA version 6.06. Tree is drawn to scale and branch lengths represent number of base differences per site (p-distance). Bootstrap (1,000 replicates) support shown for major branches.

Fig. 2. Genealogical relationships among 11 cytochrome oxidase subunit 1 in Population genetics of Oligonychus perseae (Acari: Tetranychidae) collected from avocados in Mexico and California

Fig. 2. Genealogical relationships among 11 cytochrome oxidase subunit 1 (COI) haplotypes detected in Oligonychus perseae populations in California, Mexico, and Costa Rica. Additional congeneric and outgroup sequences were retrieved from GenBank. Maximum likelihood tree constructed from a 305 base pair section of COI using PhyML. Support (aLRT) for major branches is shown.

Fig. 3 in Rapid detection of insecticide resistance in Diaphorina citri (Hemiptera: Liviidae) populations, using a bottle bioassay

Fig. 3. Susceptibility of laboratory and field-collected populations of Diaphorina citri to imidacloprid tested at the diagnostic exposure time–concentration combination (A: Lake Alfred 1; B: Winter Garden; C: Lake Alfred 2; D: Frostproof; LB: laboratory strain, FL: Florida field population). Each bar represents mean ± SE. An asterisk (*) indicates significant difference between laboratory and field population at a time period based on a Bonferroni test (P ≤ 0.05).

Fig. 2 in Rapid detection of insecticide resistance in Diaphorina citri (Hemiptera: Liviidae) populations, using a bottle bioassay

Fig. 2. Susceptibility of laboratory and field-collected populations of Diaphornia citri to dimethoate tested at the diagnostic exposure time–concentration combination (A: Lake Alfred 1; B: Winter Garden; C: Lake Alfred 2; D: Frostproof; LB: laboratory strain, FL: Florida field population). Each bar represents mean ± SE. An asterisk (*) indicates significant difference between laboratory and field population based on a Bonferroni test (P ≤ 0.05).

Fig. 1 in Rapid detection of insecticide resistance in Diaphorina citri (Hemiptera: Liviidae) populations, using a bottle bioassay

Fig. 1. Susceptibility of laboratory and field-collected populations of Diaphorina citri of bifenthrin tested at the diagnostic exposure time–concentration combination (A: Lake Alfred 1; B: Winter Garden; C: Lake Alfred 2; D: Frostproof;LB:laboratory strain, FL: Florida field population). Each bar represents mean ± SE.An asterisk (*) indicates significant difference between laboratory and field population at a time period based on a Bonferroni test (P ≤ 0.05).

Fig. 4 in Rapid detection of insecticide resistance in Diaphorina citri (Hemiptera: Liviidae) populations, using a bottle bioassay

Fig. 4. Susceptibility of laboratory and field-collected populations of Diaphorina citri to fenpropathrin tested at the diagnostic exposure time–concentration combination (A: Lake Alfred 1; B: Winter Garden; C: Lake Alfred 2; Frostproof; LB: Laboratory strain, FL: Florida Field strain). Each bar represents mean ± SE. An asterisk (*) indicates significant difference between laboratory and field population at a time period based on a Bonferroni test (P ≤ 0.05).

Fig. 1 in Population genetics of Oligonychus perseae (Acari: Tetranychidae) collected from avocados in Mexico and California

Fig. 1. Map showing Oligonychus perseae collection sites (filled circles) from California (USA), Mexico, and Costa Rica (gray areas). See Table 1 for further site details.

Fig. 1 in Effect of temperature on the population growth of Tirathaba rufivena (Lepidoptera: Pyralidae) on Areca catechu (Arecaceae)

Fig. 1. Survival rates for immature stages and the entire development period (egg to adult) of Tirathaba rufivena at 5 constant temperatures. Each value represents the mean of 3 replicates for each temperature, and bars indicate the standard error.

Fig. 2 in Effect of temperature on the population growth of Tirathaba rufivena (Lepidoptera: Pyralidae) on Areca catechu (Arecaceae)

Fig. 2. Mean numbers of eggs deposited per Tirathaba rufivena female at 5 constant temperatures. Each value represents the mean of 3 replicates for each temperature, and bars indicate the standard error.

Fig. 11 in Trypanosomes genetic diversity, polyparasitism and the population decline of the critically endangered Australian marsupial, the brush tailed bettong or woylie (Bettongia penicillata)

Fig. 11. Transmission electron micrograph of an epimastigote and an amastigote of G2 (Clade A). (A) Epimastigote in culture; Ax: Axoneme showing nine doublets of microtubules surrounding a central pair; Ac: Acidocalcisomes; Arrow: Subpellicular microtubules. (B) Amastigote inside a VERO cell. Scale bars = 0.5 µm (A), 1 µm (B).

Fig. 9 in Trypanosomes genetic diversity, polyparasitism and the population decline of the critically endangered Australian marsupial, the brush tailed bettong or woylie (Bettongia penicillata)

Fig. 9. Infection of Vero (A) and L6 cells (B) with G2 (Clade A) and T. cruzi as a positive control of infection (Diff-Quick stained). (A) Intracellular amastigotes of G2. (B) Intracellular amastigotes of T. cruzi. Scale bars = 10 µm.

Fig. 8 in Trypanosomes genetic diversity, polyparasitism and the population decline of the critically endangered Australian marsupial, the brush tailed bettong or woylie (Bettongia penicillata)

Fig. 8. Epimastigotes of G1 and G2 (Clade A) arranged in rosettes in culture. (A) Diff-Quick stained rosettes. (B) Rosettes in fresh wet preparations showing numerous intracellular acidocalcisomes. Scale bars = 10 µm.

Fig. 7 in Trypanosomes genetic diversity, polyparasitism and the population decline of the critically endangered Australian marsupial, the brush tailed bettong or woylie (Bettongia penicillata)

Fig. 7. Light microscopy of Diff-Quick stained blood and culture forms of G1 and G2 (Clade A) (A) Trypomastigote in blood of a woylie naturally infected; (B) slender epimastigote in culture; (C and D) shaped epimastigote in culture; (E) spheromastigote in culture; (F) spheromastigotes dividing in culture. Scale bars = 10 µm.