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62 results for “Chrysoperla”
Fig. 2 in Lethal and sub-lethal effects of Beauveria bassiana (Cordycipitaceae) strain NI8 on Chrysoperla rufilabris (Neuroptera: Chrysopidae)
Fig. 2. Cumulative mortality of Chrysoperla rufilabris females at 3, 5, and 10 d exposed to Beauveria bassiana strain NI8 at different concentrations (spores per mm2) under laboratory conditions. Insects were fed with a Lygus species solid diet afer being sprayed with fungus. Columns within the group labeled with a different letter were significant different at P = 0.05 (Tukey Honest Significant Difference test).
Fig. 1 in Effect of Mexican Hirsutella citriformis (Hypocreales: Ophiocordycipitaceae) strains on Diaphorina citri (Hemiptera: Liviidae) and the predators Chrysoperla rufilabris (Neuroptera: Chrysopidae) and Hippodamia convergens (Coleoptera: Coccinellidae)
Fig. 1. Overall mean mortality of Diaphorina citri adults caused by conidia of 8 Hirsutella citriformis strains applied by contact (3 separate bioassays) under controlled conditions (26 ± 1 °C, 76 ± 4% RH, 16:8 h L:D photoperiod). Error bars represent the standard error (n = 7).
Fig. 3 in Effect of Mexican Hirsutella citriformis (Hypocreales: Ophiocordycipitaceae) strains on Diaphorina citri (Hemiptera: Liviidae) and the predators Chrysoperla rufilabris (Neuroptera: Chrysopidae) and Hippodamia convergens (Coleoptera: Coccinellidae)
Fig. 3. Mean mortality of Diaphorina citri caused by blastospores of 5 Hirsutella citriformis strains under controlled conditions (26 ± 1 °C, 76 ± 4% RH, 16:8 h L:D photoperiod) during 26 d post inoculation. Different letters indicate significant differences (Tukey's test, α = 0.05). Error bars represent the standard error (n = 7).
Figure 3 in Compatibility between the predators Cryptolaemus montrouzieri (Coleoptera: Coccinellidae) and Chrysoperla externa (Neuroptera: Chrysopidae) in the control of Planococcus citri (Hemiptera: Pseudococcidae) associated with rose crop
Figure 3 Behavior of Chrysoperla externa and Cryptolaemus montrouzieri acting in combination, against adult females of Planococcus citri. *Time averages (%) followed by the same letters do not differ by Tukey's Test, P <0.05. Lowercase letters compare predators within each category; uppercase letters compare each predator individually across categories.
Figure 2 in Compatibility between the predators Cryptolaemus montrouzieri (Coleoptera: Coccinellidae) and Chrysoperla externa (Neuroptera: Chrysopidae) in the control of Planococcus citri (Hemiptera: Pseudococcidae) associated with rose crop
Figure 2Behavior of Chrysoperla externa against nymphs and adult females of Planococcus citri. Time averages (%) followed by the same letter do not differ by Tukey's test, P <0.05.
Figure 4 in Compatibility between the predators Cryptolaemus montrouzieri (Coleoptera: Coccinellidae) and Chrysoperla externa (Neuroptera: Chrysopidae) in the control of Planococcus citri (Hemiptera: Pseudococcidae) associated with rose crop
Figure 4 Behavior of Chrysoperla externa and Cryptolaemus montrouzieri acting in combination, against first instar nymphs of Planococcus citri. *Time averages (%) followed by the same letters do not differ by Tukey's Test, P <0.05. Lowercase letters compare predators within each category; uppercase letters compare each predator individually across categories.
Fig. 2 in Susceptibility of first instar Hippodamia convergens (Coleoptera: Coccinellidae) and Chrysoperla rufilabris (Neuroptera: Chrysopidae) to the insecticide sulfoxaflor
Fig. 2. Proportion of mortality (A) and developmental time (B) of Hippodamia convergens life stages afer exposure of first instars to dried insecticide residues. Afer exposure, individuals were reared to adults (L1, L2, L3, and L4 represent first, second, third, and fourth instars, respectively, and total represents first instar to adult). Within life stages, treatment means with the same letter are not significantly different (Tukey HSD, P> 0.05). FR = field rate of insecticide. Asterisks (*) indicate zeros.
Figure 2 in Inter - and intraspecific relationships between Macrosiphum rosae (Hemiptera: Aphididae) and Chrysoperla externa (Neuroptera: Chrysopidae)
Figure 2 Accumulated predatory efficiency and survival of Chrysoperla externa larvae fed aphids at different ages (A) (I - 2nd and 3rd instars; II - 4th instar and adults) of Macrosiphum rosae, according to the predator:prey ratio (Ra) and aphid density 24 (a, b), 48 (c, d), and 72 hours (e, f) after the release of the species. Different letters indicate significant differences between treatments according to Tukey's multicomparison test (p <0.05) (GLM, quasibinomial).
Figure 1 in Inter - and intraspecific relationships between Macrosiphum rosae (Hemiptera: Aphididae) and Chrysoperla externa (Neuroptera: Chrysopidae)
Figure 1 Mean daily number (± SE) of younger (second- and third-instar) and older (fourth-instar and adult) Macrosiphum rosea specimens consumed by first-, second-, and third-instar larvae of Chrysoperla externa. Different letters above the columns, uppercase for the larval stages of the chrysopid and lowercase for the aphid ages, indicate significant differences between the treatments according to Tukey's multicomparison test (p <0.05). L1, L2, and L3 = larvae of the first, second, and third instars of the chrysopid; N2-3 = second- and third-instar nymphs of the aphid; N4-Adult = fourth-instar and adult aphids.
Figure 3 in Trophic relationship between Chrysoperla externa (Neuroptera: Chrysopidae) and Planococcus citri (Hemiptera: Pseudococcidae) associated with rose bushes
Figure 3 Proportion of second-instar larvae of Chrysoperla externa survivors as a function of the density of second-instar nymphs of Planococcus citri supplied as prey and as a function of the predator:prey ratio after 24 (A) and 48 hours (B) of interaction between species. Different letters indicate significant differences by Tukey's multicomparison test (p <0.05).
Figure 2 in Trophic relationship between Chrysoperla externa (Neuroptera: Chrysopidae) and Planococcus citri (Hemiptera: Pseudococcidae) associated with rose bushes
Figure 2 Proportion of second-instar nymphs of Planococcus citri consumed by second-instar larvae of Chrysoperla externa as a function of the nymph density of the mealybug and predator:prey ratio. Different letters at the end of the curves indicate significant differences by Tukey's multicomparison test (p <0.05).
Figure 1 in Trophic relationship between Chrysoperla externa (Neuroptera: Chrysopidae) and Planococcus citri (Hemiptera: Pseudococcidae) associated with rose bushes
Figure 1 Mean (A) and total (B) number of second-instar nymphs of Planococcus citri consumed by first-, second-, and third-instar larvae of Chrysoperla externa (mean ± SE). Different letters in a column indicate significant differences by Dunn's multicomparison test (p <0.05).
Fig. 2 in Predation capability of Hippodamia convergens (Coleoptera: Coccinellidae) and Chrysoperla carnea (Neuroptera: Chrysopidae) feeding of Melanaphis sacchari (Hemiptera: Aphididae)
Fig. 2. Average of consumption rate (in %) of aphids by larvae and adults of Hippodamia convergens when allowed to freely forage 100 aphids for a period of 30 or 60 min. Larvae had a higher consumption rate, compared to adults, only for the 30-min period (t = −2.99; P = 0.0400).
Fig. 1 in Predation capability of Hippodamia convergens (Coleoptera: Coccinellidae) and Chrysoperla carnea (Neuroptera: Chrysopidae) feeding of Melanaphis sacchari (Hemiptera: Aphididae)
Fig. 1. Average consumption rate by adult males and females of the convergent ladybeetle (Hippodamia convergens) when allowed to freely forage for 24 h at different prey densities (4, 8, 16, 32, 64, or 128 aphids). The only statistical difference was found at density of 64 aphids (t = 3.625; P = 0.0222).
Figure 6 in Courtship song of the South African lacewing Chrysoperla zastrowi (Esben-Petersen) (Neuroptera: Chrysopidae): evidence for a trans-equatorial geographic range?
Figure 6. Scatterplot of the first two roots of a discriminant function analysis of nine song features (see text) of Cc5, C. zastrowi, C. lucasina, C. mediterranea and C. agilis. Each data point represents a single individual, coded by taxon.
Figure 2 in Courtship song of the South African lacewing Chrysoperla zastrowi (Esben-Petersen) (Neuroptera: Chrysopidae): evidence for a trans-equatorial geographic range?
Figure 2. Oscillograms (volts on y-axis) and sonagrams (Hertz on y-axis) of typical solo (non-dueting) vibrational songs. (A) Cc5, five volleys or shortest repeated units (SRUs); (B) Cc5, detail of a single volley/SRU; (C) C. zastrowi, five volleys or shortest repeated units (SRUs), drawn to same time scale as A. Song features discussed in the text are labeled.
Figure 4 in Courtship song of the South African lacewing Chrysoperla zastrowi (Esben-Petersen) (Neuroptera: Chrysopidae): evidence for a trans-equatorial geographic range?
Figure 4. Two key morphological features of lacewing taxa. (A) Fore wing of Cc5 (above) and C. zastrowi (beneath). Note the contrasting perpendicular versus oblique orientation of the Rs-M crossvein in the two taxa. (B) Lateral view of the lip/chin of sternite 8+9 of the male abdominal apex. Letters A–G represent landmarks used to determine relative shapes and sizes of the lip and chin. All specimens of both Cc5 and C. zastrowi showed line segment AB.BC, indicating a relatively broad, protruding lip.
Figure 3 in Courtship song of the South African lacewing Chrysoperla zastrowi (Esben-Petersen) (Neuroptera: Chrysopidae): evidence for a trans-equatorial geographic range?
Figure 3. Oscillograms comparing typical heterosexual duets, drawn to the same time scale. (A) Cc5; (B) C. zastrowi. Note the presence of occasional transient volley breaks (arrows) in the songs of both taxa.
Figure 1 in Courtship song of the South African lacewing Chrysoperla zastrowi (Esben-Petersen) (Neuroptera: Chrysopidae): evidence for a trans-equatorial geographic range?
Figure 1. Map of Africa and Middle East showing collecting localities of Cc5, C. zastrowi and specimens closely resembling those taxa.
Figure 7 in Courtship song of the South African lacewing Chrysoperla zastrowi (Esben-Petersen) (Neuroptera: Chrysopidae): evidence for a trans-equatorial geographic range?
Figure 7. Dorsal view of left half of third-instar larval head capsules. (A)–(C) Cc5 from Eilat, Israel; (D) C. zastrowi from Cedarberg, South Africa. Head markings discussed in the text are labeled. In Cc5, the most common condition for head markings is shown in B.
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