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85 results for “Diaphorina”
Fig. 1 in Feeding and oviposition of Diaphorina citri (Hemiptera: Liviidae) on Helietta apiculata (Sapindales: Rutaceae): a potential host?
Fig. 1. Survivorship of adults of Diaphorina citri on 2 rutaceous species. Means followed by the same letter did not differ in the glm test by quasi-binomial distribution (F = 5.126; df = 1,19; P = 0.036).
Fig. 2 in Feeding and oviposition of Diaphorina citri (Hemiptera: Liviidae) on Helietta apiculata (Sapindales: Rutaceae): a potential host?
Fig. 2. Mean number of eggs laid on 2 rutaceous species by Diaphorina citri during 72 h. Means followed by the same letter did not differ in the glm test by quasi-Poisson distribution (F = 14.723, df = 1,19; P = 0.012).
Figura 1 in Insecticidas de bajo impacto ambiental para el control de Diaphorina citri Kuwayama, 1908 (Hemiptera: Liviidae) en limón mexicano (Citrus aurantifolia (Christm.) Swingle)
Figura 1. Homogeneidad de varianzas de los datos de infestación. / Homogeneity of variances of the infestation data.
Fig. 1 in Occurrence of coccinellids that prey on Diaphorina citri (Hemiptera: Liviidae) on Euphorbia heterophylla (Euphorbiaceae) and Chamaecrista fasciculata (Fabaceae) in a south Florida residential area
Fig. 1. Nectary plants monitored for presence of coccinellids. (A) Chamaecrista fascisculata foliage. (B) Euphorbia heterophylla with adult Harmonia axyridis. Arrows show nectaries.
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.
Fig. 5 in Two parasitoids of Diaphorina citri (Hemiptera: Liviidae) have shared, stage-specific preference for host nymphs that does not impact pest mortality rates
Fig. 5. Mean (± SE) development time of parasitoid eggs to adult emergence of (A) Diaphorencyrtus aligarhensis and (B) Tamarixia radiata that developed on different Diaphorina citri instars in no-choice experiments. Treatment means with the same letters are not significantly different (P> 0.05).
Fig. 3 in Two parasitoids of Diaphorina citri (Hemiptera: Liviidae) have shared, stage-specific preference for host nymphs that does not impact pest mortality rates
Fig. 3. Mean (± SE) emergence of adult Diaphorencyrtus aligarhensis from second through fifh instar Diaphorina citri nymphs in no-choice experiments when females foraged alone or with hetero- and conspecific competitors. Foraging scenario only affected parasitoid emergence when D. aligarhensis foraged for fourth instar D. citri nymphs (means with the same letters are not significantly different; P> 0.05).
Fig. 2 in Two parasitoids of Diaphorina citri (Hemiptera: Liviidae) have shared, stage-specific preference for host nymphs that does not impact pest mortality rates
Fig. 2. The effect of foraging scenario on mean (± SE) Diaphorina citri mortality when (A) second, (B) third, (C) fourth, and (D) fifh instar Diaphorina citri nymphs were exposed to female parasitoids in no-choice experiments. In each panel, means with the same letters are not significantly different (P> 0.05).
Fig. 1 in Two parasitoids of Diaphorina citri (Hemiptera: Liviidae) have shared, stage-specific preference for host nymphs that does not impact pest mortality rates
Fig. 1. Mean (± SE) proportion of oviposition events (αi), indicating preference of female parasitoids for second through fifh instar Diaphorina citri nymphs in choice arenas. For each parasitoid species, means with the same letters are not significantly different (P> 0.05).
Fig. 4 in Two parasitoids of Diaphorina citri (Hemiptera: Liviidae) have shared, stage-specific preference for host nymphs that does not impact pest mortality rates
Fig. 4. Mean (± SE) adult Tamarixia radiata emergence from second through fifh instar Diaphorina citri nymphs in no-choice experiments. Means with the same letters are not significantly different (P> 0.05). *Only 1 F1 Tamarixia radiata emerged from second instar D. citri nymphs (mean [± SE] = 0.028 ± 0.028 F1 adults).
Fig. 6 in Two parasitoids of Diaphorina citri (Hemiptera: Liviidae) have shared, stage-specific preference for host nymphs that does not impact pest mortality rates
Fig. 6. The survival probability of adult (A) Diaphorencyrtus aligarhensis and (B) Tamarixia radiata that emerged from second, third, fourth, and fifh instar Diaphorina citri nymphs in no-choice experiments.
Figure 2-5. Diaphorina citri and tree damage. 2 in First record of Diaphorina citri Kuwayama (Hemiptera: Psyllidae) from the Sultanate of Oman
Figure 2-5. Diaphorina citri and tree damage. 2) D. citri infested tree (Barka). 3) Distorted acid lime leaves. 4) Adult of D. citri (lateral view). 5) Sooty mold on acid lime leaves.
Figure 1 in A checklist of natural enemies of Diaphorina citri Kuwayama (Hemiptera: Liviidae) in the department of Valle del Cauca, Colombia and the world
Figure 1. Natural enemies associated with Diaphorina citri in Colombia. Coleoptera: Coccinellidae: A. Azya orbigera Mulsant, B. Cheilomenes sexmaculata (Fabricius), C. Chilocorus cacti (L.), D. Curinus colombianus Chapin, E. Cycloneda sanguinea (L.), F. Harmonia axyridis (Pallas), G. Hippodamia convergens (Guerin-Meneville). H. Olla v-nigrum (Mulsant), I. Scymnus rubicundus Erichson. Diptera: Syrphidae: J. Allograpta (Fazia) CR-2 aff. hians, K. Leucopodella sp. Hemiptera: Reduviidae: L. Zelus cf. nugax Stål, Hymenoptera: Vespidae: M. Polybia sp. Eulophidae: N. Tamarixia radiata (Waterston). Neuroptera: Chrysopidae: O. Ceraeochrysa sp.
Figs 4–7 in Aphasmaphleps, a new genus of long-legged flies from Senegal, with a key to the genera of Afrotropical Diaphorinae (Diptera: Dolichopodidae)
Figs 4–7. Details of A. bandia sp. n.: (4–6) Tarsi: (4) fore tarsus, (5) mid tarsus laterally, (6) mid tarsus dorsolaterally; (7) Hypopygium, left lateral aspect. Abbreviations: cer – cercus, ep – epandrium, epl – epandrial lobe, hyp – hypandrium, ph – phallus, pgt – postgonite, dsur, vsur – surstylus (dorsal and ventral lobes). Scale bars: 0.2 mm (Figs 4–6), 0.3 mm (Fig. 7).
Figs 8, 9 in Aphasmaphleps, a new genus of long-legged flies from Senegal, with a key to the genera of Afrotropical Diaphorinae (Diptera: Dolichopodidae)
Figs 8, 9. Habitus of Falbouria acorensis (Parent, 1933) and its head, holotype. Scale bars: 1 mm (Fig. 8), 0.5 mm (Fig. 9).
Figs 1−3. A in Aphasmaphleps, a new genus of long-legged flies from Senegal, with a key to the genera of Afrotropical Diaphorinae (Diptera: Dolichopodidae)
Figs 1−3. A. bandia sp. n.: (1) habitus, (2) wing, (3) head. Scale bars: 0.5 mm (Fig. 1), 0.2 mm (Figs 2, 3).
Figs 1–5 in Unusual behaviour - unusual morphology: mutualistic relationships between ants (Hymenoptera: Formicidae) and Diaphorina enderleini (Hemiptera: Psylloidea), associated with Vernonia amygdalina (Asteraceae)
Figs 1–5. Fifth instar larva of Diaphorina enderleini: (1) habitus, dorsal surface left, ventral surface right; (2) detail of forewing pad, outer margin; (3) antenna; (4) tarsus with claws and tarsal arolium; (5) caudal plate, dorsal surface left, ventral surface right.
Figs 6–10. Ants attending D in Unusual behaviour - unusual morphology: mutualistic relationships between ants (Hymenoptera: Formicidae) and Diaphorina enderleini (Hemiptera: Psylloidea), associated with Vernonia amygdalina (Asteraceae)
Figs 6–10. Ants attending D. enderleini on V. amygdalina leaves: (6) shelter enclosing psyllid larvae and Pheidole megacephala workers; (7) psyllid females and eggs with P. megacephala workers; (8) psyllid females and larvae with Crematogaster striatula workers and carton shelter's remains; (9) psyllid females and eggs with Camponotus acvapimensis workers; (10) psyllid larvae with Myrmicaria opaciventris workers.
MS/MS proteomics from: <em>Citrus sinensis</em> leaves in response to Diaphorina citri infestation and Huanglongbing disease
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1H NMR based metabolomics from: <em>Citrus sinensis</em> leaves in response to Diaphorina citri infestation and Huanglongbing disease
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