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60 results for “Diaphorina citri”
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. 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.
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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High quality, chromosome-scale genome assemblies: Comparisons of three Diaphorina citri (Asian Citrus Psyllid) geographic populations
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Diaphorina citri new genome annotations and GO terms (2021)
<p>Additional genome annotations for the <em>Diaphorina citri</em> genome (Diaci_v3) including: TEs, intergenic regions and putative promotors, also additional gene ontology terms annotated using EGGnog. </p>
Fig. 1 in Feeding behavior of Diaphorina citri (Hemiptera: Liviidae) and its acquisition of 'Candidatus Liberibacter asiaticus', on huanglongbing-infected Citrus reticulata leaves of several maturity stages
Fig. 1. Sketches of citrus leaves at several maturity stages.
Infection with 'Candidatus Liberibacter asiaticus' improves the fecundity of Diaphorina citri aiding its proliferation: a win-win strategy
<p>The coevolution between insect vectors and pathogens has long been of interest in molecular ecology and evolutionary biology, and <em>Diaphorina citri</em> is the main insect vector of the bacterium, ‘<em>Candidatus</em> Liberibacter asiaticus’ (<em>C</em>Las), the putative cause of the severe Asian form of huanglongbing. <em>C</em>Las-positive <em>D. citri</em> are more fecund than their <em>C</em>Las-negative counterparts; however, the molecular mechanism underlying of increased fecundity remains unclear. Here, we found that <em>C</em>Las promoted ovarian development and increased the expression of the <em>vitellogenin</em> <em>receptor</em> (<em>Dc</em><em>VgR</em>) in ovaries. <em>Dc</em><em>VgR</em> RNAi significantly decreased fecundity and <em>C</em>Las titer in ovaries, extended the preoviposition period, shortened the oviposition period, and blocked ovarian development. Combined <em>in vivo</em> and <em>in vitro</em> experiments showed that miR-275 suppressed <em>Dc</em><em>VgR</em> expression by binding to its 3’ untranslated region. Overexpression of miR-275 resulted in a decline of <em>Dc</em><em>VgR</em> expression and <em>C</em>Las titer in ovaries and caused reproductive defects that mimicked <em>Dc</em><em>VgR</em> knockdown phenotypes. After infection with <em>C</em>Las, the juvenile hormone (JH) signaling pathway was upregulated thereby increasing <em>Dc</em><em>VgR</em> expression via the JH receptor, <em>methoprene-tolerant</em> (Met), and downstream key transcription factor <em>Krüppel homolog 1</em>. As a result, <em>C</em>Las hijacks the JH signaling pathway and host miR-275 that targets <em>Dc</em><em>VgR</em> to improve <em>D. citri</em> fecundity, while simultaneously increasing the replication of <em>C</em>Las itself, suggesting a mutualistic interaction in <em>D. citri </em>ovaries with <em>C</em>Las.</p>
Data from: Insect-microbe-fungus interplay in citrus agro-ecosystems: Cuticular symbionts mediate <em>Diaphorina citri</em> resistance to <em>Beauveria bassiana</em>
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Host Finding Disruption of Diaphorina Citri by Guava Shoot Extract and Menochilus Sexmaculatus
<div> <p>This material has presented on 2nd International Conference on Advance Research in Agriculture and Food 2023 in October 25, 2023.</p> </div>
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