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62 results for “Chrysoperla”
Figure 2 in The most important lacewing species in Indian agricultural crops, Chrysoperla sillemi (Esben-Petersen), is a subspecies of Chrysoperla zastrowi (Esben-Petersen) (Neuroptera: Chrysopidae)
Figure 2. Oscillogram (volts on y-axis) and sonogram (Hertz on y-axis) of five volleys of a solo (non-duetting) vibrational song of Chrysoperla sillemi (now C. z. sillemi) from Bangalore, India. During heterosexual duets, each volley is the unit of exchange between partners (i.e. the shortest repeated unit or SRU). Song features discussed in the text are labelled.
Figure 4 in The most important lacewing species in Indian agricultural crops, Chrysoperla sillemi (Esben-Petersen), is a subspecies of Chrysoperla zastrowi (Esben-Petersen) (Neuroptera: Chrysopidae)
Figure 4. Dorsal view of left half of third-instar larval head capsule of a typical specimen of Chrysoperla sillemi (now Chrysoperla zastrowi sillemi) from Bangalore, India. Head markings discussed in the text are labelled.
Figure 1 in The most important lacewing species in Indian agricultural crops, Chrysoperla sillemi (Esben-Petersen), is a subspecies of Chrysoperla zastrowi (Esben-Petersen) (Neuroptera: Chrysopidae)
Figure 1. Map of central and southwest Asia showing collecting localities of Chrysoperla sillemi (circled numbers or letters) in India and Chrysoperla zastrowi arabica (black circles) in the Middle East, identified by song analysis. Both taxa are now assigned to Chrysoperla zastrowi sillemi stat. rev. Locality 1 = Ludhiana (Punjab); 2 = Sirsa (Haryana); 3 = Anand (Gujarat); 4 = Bangalore (Karnataka); 5 = Coimbatore (Tamil Nadu); a = Sri Ganganagar (Rajasthan); b = Udaipur (Rajasthan); c = Dharwad (Karnataka) and d = Guntur (Andhra Pradesh). Songs were analysed in detail only for specimens from the numbered (not lettered) sites on the map. Collecting localities of additional specimens exhibiting the C. z. sillemi morphotype but not verified by song are shown as black asterisks.
Figure 3 in The most important lacewing species in Indian agricultural crops, Chrysoperla sillemi (Esben-Petersen), is a subspecies of Chrysoperla zastrowi (Esben-Petersen) (Neuroptera: Chrysopidae)
Figure 3. Scatterplot of the first two factors of a principal components analysis of five song features (see text) of Chrysoperla sillemi in India (black squares) and Chrysoperla zastrowi arabica in the Middle East (open triangles). Both taxa are now assigned to Chrysoperla zastrowi sillemi stat. rev. Each data point represents a single individual.
Fig. 3 in Susceptibility of Chrysoperla externa (Hagen, 1861) (Neuroptera: Crysopidae) to insecticides used in coffee crops
Fig. 3 Survival of Chrysoperla externa exposed to insecticides used in coffee crop. a Pupal stage (df = 2, Χ2 = 100.23, p> 0.05), group 1 = azadirachtin, ethiprole and teflubenzuron; group 2 = chlorpyrifos, and group 3 = control. b Adults (df = 2, Χ2 = 224.83, p> 0.05); group 1 = azadirachtin and control; group 2 = ethiprole and teflubenzuron, and group 3 = chlorpyrifos
Fig. 4 in Susceptibility of Chrysoperla externa (Hagen, 1861) (Neuroptera: Crysopidae) to insecticides used in coffee crops
Fig. 4 Reproductive parameters of Chrysoperla externa exposed to insecticides used in coffee crop. a Mean number of eggs oviposited by females (SE) exposed to insecticides when pupae (df = 3, Χ² = 247.3, p <0.05) and adults (df = 2, F = 8.1353, p <0.05. b Total eggs layed by females exposed to insecticides when pupae (df = 3, F = 29.756, p <0.05) and adults (df = 2, F = 53.006, p <0.05). c Egg viability (SE) of females exposed to insecticides when pupae (df = 3, F = 3.4328, p <0.05) and adults (ns = the means do not differ from each other, df = 2, F = 1.5769, p> 0.05)
Fig. 2 in Susceptibility of Chrysoperla externa (Hagen, 1861) (Neuroptera: Crysopidae) to insecticides used in coffee crops
Fig. 2 Number of males and females (SE) of Chrysoperla externa adults from pupae exposed to insecticides (ns = the means do not differ from each other, df = 3, Χ2 = 0.093936, p> 0.05)
Fig. 1 a in Susceptibility of Chrysoperla externa (Hagen, 1861) (Neuroptera: Crysopidae) to insecticides used in coffee crops
Fig. 1 a Percentage of adults emergence of Chrysoperla externa from pupae exposed to insecticides (df = 4, F = 7.3237, p> 0.05). b Duration of the pupal stage in days, when insects exposed to insecticides while pupae of C. externa (ns = the means do not differ from each other, df = 4, F = 1.3462, p> 0.05)
Fig. 1 in Lethal and sub-lethal effects of Beauveria bassiana (Cordycipitaceae) strain NI8 on Chrysoperla rufilabris (Neuroptera: Chrysopidae)
Fig. 1. Fertility table data and reproductive values of Chrysoperla rufilabris females 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. A. Survival probability at age x (lx) (p = 0.05, LIFETEST of Equality over Strata); B. Net fecundity (lxmx); and C. Reproductive value (Vx).
Figuras 1a-b. Chrysoperla asoralis. a in Primer reporte de dos especies de Chrysoperla Steinmann, 1964 (Neuroptera: Chrysopidae) asociadas a cítricos en Chile
Figuras 1a-b. Chrysoperla asoralis. a. Cabeza de la larva de segundo estadio en vista dorsal. b. Cabeza del adulto en vista lateral. / 1a-b. Chrysoperla asoralis. a. Head of second instar larva in dorsal view. b. Adult head in lateral view. Figuras 1c-d. Chrysoperla argentina. c. Cabeza de la larva de segundo estadio en vista dorsal. d. Cabeza del adulto en vista lateral. / 1c-d. Chrysoperla argentina. c. Head of second instar larva in dorsal view. d. Adult head in lateral view.
Figure 1 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 1 Behavior of Cryptolaemus montrouzieri 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.
Fig. 5-6 in Description of a new species of Chrysoperla STEINMANN, 1964 of the Ch. mediterranea HÖLZEL, 1972 group from Europe (Neuropterida, Neuroptera, Chrysopidae)
Fig. 5-6: (5) Internal genitalia: Chrysoperla europaea (right, after BROOKS, 1994 erroneously labelled Chrysoperla mediterranea), gonarcus complex lateral view (left), dorsal view (middle), tignum dorsal (down); and of Ch. mediterranea (left) (after HÖLZEL, 1972). Scales not appointed; (6) male abdominal terminalia of Chrysoperla europaea (scale bar = 1 mm).
Sodalis assembly from Chrysoperla carnea
<p>Draft genome of the endosymbiont <em>Sodalis</em> in the common green lacewing (<em>Chrysoperla carnea</em>). DNA was extracted from a adult <em>Chrysoperla carnea</em> from a laboratory culture, originated from the company Sauter and Stepper. DNA was sequenced with Illumina HiSeq 2500 and the assembly was created using SPAdes.</p>
Figure 1 in Is a diet of Planococcus citri nymphs and adults suitable for Chrysoperla externa for use in biological control?
Figure 1. Duration of instars and preimaginal phases (days) of Chrysoperla externa as a function of feeding on Ephestia kuehniella eggs and/or Planococcus citri nymphs and adults. Means ± SE corresponding to the columns paired under the horizontal bar do not differ by the Dunn test (Kruskal-Wallis, p<0.05). L1= 1st instar larvae; L2= 2nd instar larvae; L3= 3rd instar larvae; PP= Prepupae; P= Pupae. EK= E. kuehniella eggs; EK + PC= E. kuehniella eggs in the first instar and P. citri in subsequent instars; PC= P. citri in all instars.
FIGURE 2 in Physiological selectivity of insecticides to eggs and larvae of predator Chrysoperla externa (HAGEN) (Neuroptera: Chrysopidae)
FIGURE 2 - Duration (days) of three larval instars and pupal stage of Chrysoperla externa, from first instar larvae treated with the pesticides. Treatments: 1: chlorpyrifos; 2: cartaphydrochloride; 3: pyriproxyfen, 4: profenofos/ lufenuron; 5: fenpropathrin; 6: deltamethrin/triazophos; 7: zetacypermethrin and 8: control.
Squash preparations and living cells showing chromosome arrangement in mitosis, meiosis I, and meiosis II in green lacewing (Chrysoperla rufilabris) males
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Figure 4 in A new lacewing species of the Chrysoperla carnea species-group from central Asia associated with conifers (Neuroptera: Chrysopidae)
Figure 4. Dorsal view of third-instar larval head capsule (left half) of Chrysoperla duellii sp. nov. The drawing represents the typical condition seen in 21 individuals raised from the eggs of adults from several populations in Kyrgyzstan. The colour insert is a typical mature third-instar larva of the species.
Figure 3 in A new lacewing species of the Chrysoperla carnea species-group from central Asia associated with conifers (Neuroptera: Chrysopidae)
Figure 3. Adult of Chrysoperla duellii sp. nov.: (a) non-diapausing green form and (b) diapausing redfaced form. Note retention of green ground colour in (b), the overwintering (diapausing) form of C. duellii.
Figure 6 in A new lacewing species of the Chrysoperla carnea species-group from central Asia associated with conifers (Neuroptera: Chrysopidae)
Figure 6. Bar graph of the probabilities of assignment to species by a Discriminant Analysis of Principal Components (DAPC) applied to individuals identified acoustically as belonging to C. duellii sp. nov., C. boltiı C. 'carnea-K', C. downesiı C. calocedrii and C. mediterranea (same species as in Figure 5). Most individuals have a very high probability of assignment to the correct species determined by morphology and bioacoustics.
Figure 1 in A new lacewing species of the Chrysoperla carnea species-group from central Asia associated with conifers (Neuroptera: Chrysopidae)
Figure 1. Oscillographs (lower of each pair of traces) and sonographs (upper traces) of (a) a solo vibrational song (shortest repeated unit or SRU) of Chrysoperla duellii sp. nov. from Kyrgyzstan in central Asia and (b) a solo vibrational song of Chrysoperla downesi from northeastern North America, illustrating convergent song phenotypes in these two completely allopatric species. Each song was recorded at 25 ± 1°C and is drawn to the same timescale of 6.25 s. For C. duellii (a), each of the four distinctly different types of volleys characteristic of this species is labelled, while for C. downesi (b), each of its two distinctive volley types is noted. Within-volley vibrational frequency declines in each type of volley of C. duellii but increases in each type of volley of C. downesi – an important diagnostic (and plainly audible) difference between the two species.
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