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Fig. 5 in Laboratory feeding responses of Euthyrhynchus floridanus and Podisus maculiventris (Hemiptera: Pentatomidae) to the kudzu bug, Megacopta cribraria (Hemiptera: Plataspidae)

Fig. 5. Mean percent predation of Megacopta cribraria by Podisus maculiventris (I) without and (II) with alternative preya.

Fig. 4 in Laboratory feeding responses of Euthyrhynchus floridanus and Podisus maculiventris (Hemiptera: Pentatomidae) to the kudzu bug, Megacopta cribraria (Hemiptera: Plataspidae)

Fig. 4. Mean percent predation of Megacopta cribraria by Euthyrhynchus floridanus (I) without and (II) with alternative preya.

Fig. 3 in Effects of dietary intake of volcanic ash from Puyehue Cordon Caulle on Tenebrio molitor (Coleoptera: Tenebrionidae) larvae under laboratory conditions

Fig. 3. Mean body weight of larvae (mg) fed 30,000 and 50,000 ppm of volcanic ash treated flour disks afer 15 d. Bars with the same letter are not significantly different α = 0.05. Bioassay endpoint = 15 d, n = 10, substrate = treated and control insect food (ANOVA: F = 93.67; df = 2; P <0.0001).

Fig. 1 in Effects of dietary intake of volcanic ash from Puyehue Cordon Caulle on Tenebrio molitor (Coleoptera: Tenebrionidae) larvae under laboratory conditions

Fig. 1. Chemical composition of ash from Puyehue Cordon Caulle eruption collected in Collón Curá, Neuquén, Argentina (40.0400°S, 70.2405°W) 15 Jun 2011, determined by energy dispersive spectroscopy. Previously published in Buteler et al. (2011), Revista de la Sociedad Entomológica Argentina 70 (3–4), Figure 3, copyright RSEA, reproduced with permission.

Fig. 6 in Effects of dietary intake of volcanic ash from Puyehue Cordon Caulle on Tenebrio molitor (Coleoptera: Tenebrionidae) larvae under laboratory conditions

Fig. 6. Molting rate of Tenebrio molitor larvae feed on flour disks treated with sub-lethal concentrations (500, 1,000, 5,000 ppm) of volcanic ash. Molting rate = number of molts per incubation period of 27 d.

Fig. 5 in Effects of dietary intake of volcanic ash from Puyehue Cordon Caulle on Tenebrio molitor (Coleoptera: Tenebrionidae) larvae under laboratory conditions

Fig. 5. Larval body length (cm) of Tenebrio molitor larvae fed on flour disks treated with sub-lethal concentrations (500, 1,000, 5,000 ppm) of volcanic ash. Bars with the same letter are not significantly different α = 0.05. Bioassay endpoint = 27 d, n = 10, substrate = treated and control insect food (ANOVA: F = 95.15; df = 3; P <0.0001).

Fig. 4 in Effects of dietary intake of volcanic ash from Puyehue Cordon Caulle on Tenebrio molitor (Coleoptera: Tenebrionidae) larvae under laboratory conditions

Fig. 4. Mean body weight of larvae (mg) fed on sub lethal concentrations (500, 1,000, 5,000 ppm) of volcanic ash treated flour disks. Bars with the same letter are not significantly different at α = 0.05. Bioassay endpoint = 27 d, n = 10, substrate = treated and control insect food (ANOVA: F = 133.97; df = 3; P <0.0001).

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.

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Fig. 3. Proportions and 95 in Metamasius callizona (Coleoptera: Curculionidae): fertility and larval survival to the third instar in the laboratory

Fig. 3. Proportions and 95% confidence intervals for egg eclosion per 10 d from eggs laid inside leaves by Metamasius callizona. Confidence intervals were calculated using Wilson score intervals (α = 0.05; Wilson 1927).

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Fig. 2 in Metamasius callizona (Coleoptera: Curculionidae): fertility and larval survival to the third instar in the laboratory

Fig. 2. Average number of eggs laid by Metamasius callizona inside, outside, and inside + outside the leaf by Metamasius callizona, with 95% confidence intervals for the first half and second half of the female reproductive periods.

opencc-by-4.0Jun 2019View details →

Fig. 1 in Metamasius callizona (Coleoptera: Curculionidae): fertility and larval survival to the third instar in the laboratory

Fig. 1. Average number of eggs laid per leaf per Metamasius callizona female per 10 d (± SE) inside and outside leaves over time.

opencc-by-4.0Apr 2020View details →

Fig. 1 in The effects of laboratory rearing diet on recruitment behavior of Wasmannia auropunctata (Hymenoptera: Formicidaea)

Fig. 1. Mean ± SE difference in recruitment rates of laboratory raised Wasmannia auropunctata to non-toxic baits: Hawaii Ant Lab gel bait, 50% gelled sucrose solution, and tuna between pre- and post-treatment measurements of the multi-choice laboratory experiment (n = 5 colonies). Bars in each group with different letters above have statistically different means (P <0.05). Colonies were exposed to their respective dietary treatment (buffet plus crickets: n=5, vegetable oil wick plus crickets: n=5, 25% sucrose solution plus crickets: n=5, and pureed tuna plus crickets: n=5) for 49 d. Means represented in this chart are based on raw data for visualization and are not the reported marginal means.

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Fig. 2 in The effects of laboratory rearing diet on recruitment behavior of Wasmannia auropunctata (Hymenoptera: Formicidaea)

Fig. 2. Recruitment rates (mean number of ants ± SE) of wild Wasmannia auropunctata to the Hawaii Ant Lab gel bait, 50% gelled sucrose solution, and tuna for multi-choice (n = 6 per treatment) and no-choice (n = 6 per treatment) field experiments. Bars within clusters with different letters above have statistically different means (P <0.05). Means represented in this chart are based on raw data for visualization and not proportional results from the Poisson distributed generalized linear mixed model as reported.

opencc-by-4.0Sep 2020View details →

Fig. 2 in Laboratory rearing of Bagrada hilaris (Hemiptera: Pentatomidae) under quarantine conditions in Florida, USA

Fig. 2. Mean number of eggs oviposited by 10 Bagrada hilaris females on dental wicks, cotton balls, or Kimwipes in no-choice and choice tests. There was a significant effect of substrate type on the number of eggs oviposited in both the no-choice (F = 7.981; df = 2; P <0.001) and choice (F = 28.61; df = 2; P <0.001) tests.

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Fig. 1 in Laboratory rearing of Bagrada hilaris (Hemiptera: Pentatomidae) under quarantine conditions in Florida, USA

Fig. 1. Large cages for no-choice and choice tests for evaluating the preference of Bagrada hilaris for 3 artificial oviposition substrates: dental wicks, cotton balls, or Kimwipes.

Fig. 4 in Assessment of the predatory capacity on mosquito larvae of Jenynsia multidentata (Anablepidae) in presence of vegetation under laboratory conditions

Fig. 4. Daily consumption (mean ±SD) of Jenynsia multidentata (Jenyns, 1842) on 120 Culex pipiens Linnaeus, 1758 fourth-stage larvae. (T1) 20 stems, (TC) without stems, for 5 days.

Fig. 2 in Assessment of the predatory capacity on mosquito larvae of Jenynsia multidentata (Anablepidae) in presence of vegetation under laboratory conditions

Fig. 2. Daily consumption (mean ±SD) of Jenynsia multidentata (Jenyns, 1842) on 60 Culex pipiens Linnaeus, 1758 fourth-stage larvae at different densities of vegetation: (T1) 20 stems, (T2) 10 stems and (TC) without stems, for 5 days.

Fig. 1 in Assessment of the predatory capacity on mosquito larvae of Jenynsia multidentata (Anablepidae) in presence of vegetation under laboratory conditions

Fig. 1. Jenynsia multidentata (Jenyns, 1842) consumption of 60 Culex pipiens Linnaeus, 1758 fourth-stage larvae at different vegetation densities: (T1) 20 stems, (T2) 10 stems and (TC) without stems. Each circle represents the daily consumption of a female specimen and the horizontal bars indicate the average consumption. The letters (a, b) at the top of the figure indicate significant differences between treatments (p <0.05).

Fig. 3 in Assessment of the predatory capacity on mosquito larvae of Jenynsia multidentata (Anablepidae) in presence of vegetation under laboratory conditions

Fig. 3. Jenynsia multidentata (Jenyns, 1842) consumption of 120 Culex pipiens Linnaeus, 1758 fourth-stage larvae at different vegetation densities: (T1) 20 stems and (TC) without stems. Each circle represents the daily consumption of a female specimen and the horizontal bars indicate the average consumption.