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1,419 results for “Eulophidae”
Figure 1 in Horismenus cupreus (Hymenoptera: Eulophidae) parasitizing Bedellia somnulentella (Lepidoptera: Bedelliidae) in Ipomoea batatas
Figure 1. Horismenus cupreus (Ashmead, 1894) (Hymenoptera: Eulophidae) parasitoid of Bedellia somnulentella Zeller, 1847 (Lepidoptera: Bedelliidae) pupae.
Fig. 2 in Susceptibility of Eucalyptus spp. (Myrtales: Myrtaceae) and clones to Leptocybe invasa (Hymenoptera: Eulophidae) in Paraná, Brazil
Fig. 2. Percentage of leaves and stems with galls caused by Leptocybe invasa in plants in each stratum (lower, middle, upper) of approx. 2-m-tall Eucalyptus spp. and clones at Umuarama, PR, Brazil, in 2013.
Fig. 1B in Reproduction of Tetrastichus howardi (Hymenoptera: Eulophidae) in Diatraea saccharalis (Lepidoptera: Crambidae) pupae at different temperatures
Fig. 1B). The maximum longevity of T. howardi was 50 d at 16 °C and the minimum was 2 d at 31 °C. The longevity of this parasitoid was 21 d at 25 °C. Tetrastichus howardi females began to oviposit on the same day they had contact with the host pupae. Parasitoid progeny production was greater when parasitism occurred during the 1st day of exposure to host pupae at all temperatures. About 90% of the offspring was pro-
Fig. 2 in Parasitism and emergence of Tetrastichus howardi (Hymenoptera: Eulophidae) on Diatraea saccharalis (Lepidoptera: Crambidae) larvae, pupae and adults
Fig. 2. Larvae, pupae and adults of Tetrastichus howardi (Hymenoptera: Eulophidae) in pupae of Diatraea saccharalis(Lepidoptera: Crambidae) (A, B, C); D. saccharalis adult parasitized by T. howardi (D).
Fig. 2 in Development of Thripastichus gentilei (Hymenoptera: Eulophidae) in the thrips Gynaikothrips uzeli (Thysanoptera: Phlaeothripidae)
Fig. 2. Survivorship function [S(t)] for Thripistichus gentilei adults provisioned with a sugar water solution, distilled water, or no food (starved) along with thrips hosts. Median survival time was greater for wasps provided sugar water compared with survival for those given either water or starved. Bars represent the standard error [SE S(t)].
Fig. 1 in Development of Thripastichus gentilei (Hymenoptera: Eulophidae) in the thrips Gynaikothrips uzeli (Thysanoptera: Phlaeothripidae)
Fig. 1. Two immatures of Gynaikothrips uzeli: the upper individual is a normal larva, and the lower one displays the transparent, swollen appearance of a parasitized larva. The parasitoid, Thripistichus gentilei, develops with a polarity that is reverse relative to the host.
Fig. 1 in Can the choice behavior and fitness of Tamarixia radiata (Hymenoptera: Eulophidae) be affected by the citrus (Sapindales: Rutaceae) variety used to rear the Asian citrus psyllid (Hemiptera: Liviidae)?
Fig. 1. Mean percentage (± SE) of parasitism of Tamarixia radiata on nymphs of Diaphorina citri reared on 4 citrus varieties. Means do not differ by Tukey's test (P> 0.05).
Fig. 2 in Foraging activity of Palmistichus elaeisis (Hymenoptera: Eulophidae) at various densities on pupae of the eucalyptus defoliator Thyrinteina arnobia (Lepidoptera: Geometridae)
Fig. 2. (A) Duraton of life cycle (egg to adult) and (B) numbers of Palmistichus elaeisis progeny with a density of 1, 3, 6, 9, 12, 15, 18, or 21 ovipositng females per Thyrinteina arnobia pupa at 25 ± 2 °C, 70 ± 10% RH, and a 12:12 h L:D photoperiod.
Fig. 1 in Foraging activity of Palmistichus elaeisis (Hymenoptera: Eulophidae) at various densities on pupae of the eucalyptus defoliator Thyrinteina arnobia (Lepidoptera: Geometridae)
Fig. 1. Percentage of pupae parasitzed and percentage of emergence of Palmistichus elaeisis with a density of 1, 3, 6, 9, 12, 15, 18, or 21 ovipositng females per Thyrinteina arnobia pupa at 25 ± 2 °C, 70 ± 10% RH, and a 12:12 h L:D photoperiod. Statstcal significance: parasitsm, P = 0.3770; emergence, P = 0.034.
Fig. 3 in Laboratory evaluations of the foraging success of Tamarixia radiata (Hymenoptera: Eulophidae) on flowers and extrafloral nectaries: potential use of nectar plants for conservation biological control of Asian citrus psyllid (Hemiptera: Liviidae)
Fig. 3. Choice of cups with either unscented sucrose solution or with bananascented sucrose solution made by Tamarixia radiata following a pre-test exposure to either 1.0 M sucrose solution or 1.0 M sucrose solution and banana flavor extract (G-test; ** = P ≤ 0.01; NS = not significant).
Fig. 1 in Laboratory evaluations of the foraging success of Tamarixia radiata (Hymenoptera: Eulophidae) on flowers and extrafloral nectaries: potential use of nectar plants for conservation biological control of Asian citrus psyllid (Hemiptera: Liviidae)
Fig. 1. Diagrammatic representation of nectary architectures presented to Tamarixia radiata in foraging evaluations. Location of nectaries shown in red. A. Cy- athium of euphorbiaceous species with exposed nectaries. B. Partially exposed nectaries as found in buckwheat. C. Partially hidden nectaries as found in alyssum. D. Partially exposed nectaries covered with trichomes as found in marjoram. E. Hidden nectaries as found in composites. Drawings are only indicative of size and spatial relationships and are not to scale.
Fig. 2 in Laboratory evaluations of the foraging success of Tamarixia radiata (Hymenoptera: Eulophidae) on flowers and extrafloral nectaries: potential use of nectar plants for conservation biological control of Asian citrus psyllid (Hemiptera: Liviidae)
Fig. 2. Mean (± SE) feeding time of Tamarixia radiata when presented with different concentrations of sugars commonly occurring in nectar (sucrose, fructose, glucose) and honeydew (melizitose, raffinose). Bars within the same concentration having different letters are different at P ≤ 0.05 (ANOVA).
Fig. 1 in Selitrichodes neseri (Hymenoptera: Eulophidae) recovered from Leptocybe invasa (Hymenoptera: Eulophidae) galls afer initial release on Eucalyptus (Myrtaceae) in Brazil, and data on its biology
Fig. 1. Municipality of Rio Real, Bahia State, where Selitrichodes neseri (Hymenoptera: Eulophidae) adults were released for the first time in Brazil.
Fig. 3 in Development and morphological characterization of the immature stages of Tetrastichus giffardianus Silvestri (Hymenoptera: Eulophidae)
Fig. 3. Immature stages of Tetrastichus giffardianus. Egg (A); first-instar larva (B, C); second-instar larva (D); third-instar larva (E); pre-pupa (F); pupa at three different stages of melanization (G, H, I). Scale bar = 0.1 mm.
Fig. 1 in Development and morphological characterization of the immature stages of Tetrastichus giffardianus Silvestri (Hymenoptera: Eulophidae)
Fig. 1. Tetrastichus giffardianus larvae (A) and pupae (B) inside a Ceratitis capitata puparium; (C) emergence of adults; (D) C. capitata puparium with T. giffardianus emergence hole.
Figure 3. L in Records of Elasmus species (Hymenoptera: Chalcidoidea: Eulophidae) from different States of India with thirteen new state records
Figure 3. L -Elasmus longiventris; M - Elasmus neoflavocorpus; N - Elasmus pulchellus; O - Elasmus punensis; P - Elasmus queenslandicus.
Figure 2. G in Records of Elasmus species (Hymenoptera: Chalcidoidea: Eulophidae) from different States of India with thirteen new state records
Figure 2. G - Elasmus homonae; H - Elasmus hyblae; I - Elasmus indicus; J - Elasmus jhonstoni; K - Elasmus longicornis.
Fig. 1 in Potential Global Range Expansion Of A New Invasive Species, The Erythrina Gall Wasp, Quadrastichus Erythrinae Kim (Insecta: Hymenoptera: Eulophidae)
Fig. 1. Potential global range of erythrina gall wasp. The gray shadow indicates the potential expanding range, and the white blank areas indicate where infestation is unlikely.
Fig. 1 in Threshold temperatures and thermal requirements of Psyllaphycus diaphorinae (Hymenoptera: Encyrtidae), a hyperparasitoid of Diaphorencyrtus aligarhensis (Hymenoptera: Encyrtidae) and Tamarixia radiata (Hymenoptera: Eulophidae)
Fig. 1. Predicted rate of total development as a function of temperature for Psyllaphycus diaphorinae (pooled males and females) at different constant and fluctuating temperatures using linear (a), Performance-2 (b), and Ratkowsky (c) models. In the linear and Perfomance-2 charts, the ordinate is the rate of development (1/D, per d), and the abscissa is temperature (°C). In the Ratkowsky chart (c) the ordinate is the square root of development rate (, per d), and the abscissa is temperature (°C). Symbols represent mean observed data. Solid lines represent model predictions for fluctuating temperatures and dashed lines for constant temperatures. For linear regression (a), data values for 32 °C were omitted because of significant deviation from rectilinearity.
Figs 1, 2 in Phenotypic matching in ovipositor size in the parasitoid Galeopsomyia sp. (Hymenoptera, Eulophidae) attacking different gall inducers
Figs 1, 2. Phenotic matching between the parasitoid Galeopsomyia sp. (Eulophidae) and its galling hosts, five species of Bruggmania (Cecidomyiidae, B. elongata, B. robusta, B. acaudata, and Bruggmania sp. 1 and sp. 2) in Guapira opposita (Nyctaginaceae): Fig. 1, gall thickness (dimension between the outer wall of the gall and the larval chamber); Fig. 2, female ovipositor length of parasitoid in the different hosts.
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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.