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Relevant bibliographies by topics / Feeding assays

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Journal articles

Academic literature on the topic 'Feeding assays'

Author: Grafiati

Published: 27 June 2023

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Journal articles on the topic "Feeding assays"

1

Shen, Ping. "PreparingDrosophilaLarvae for Feeding Assays." Cold Spring Harbor Protocols 2012, no. 5 (2012): pdb.prot069302. http://dx.doi.org/10.1101/pdb.prot069302.

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2

Peters, Brenton C. "Xylophagous insects: developments in feeding assays." Australian Journal of Entomology 44, no. 2 (2005): 214–15. http://dx.doi.org/10.1111/j.1440-6055.2005.00477.x.

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3

Kröber, Thomas, and Patrick M. Guerin. "In vitro feeding assays for hard ticks." Trends in Parasitology 23, no. 9 (2007): 445–49. http://dx.doi.org/10.1016/j.pt.2007.07.010.

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4

Zavala H., Andrea, Emilio Hormazabal U., Gloria Montenegro R., et al. "Effects of extracts from Maytenus on Aegorhinus superciliosus (Coleoptera: Curculionidae) and Hippodamia convergens (Coleoptera: Coccinellidae)." Revista Colombiana de Entomología 43, no. 2 (2017): 233. http://dx.doi.org/10.25100/socolen.v43i2.5948.

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The insecticidal effects of five ethanolic extracts produced from three species of the genus Maytenus: M. boaria leaf (MBL), M. boaria bark (MBB), M. boaria seed (MBS), M. disticha leaf (MDL) and M. magellanica leaf (MML) were evaluated on the lady beetle Hippodamia convergens (Coleoptera: Coccinellidae) and on the pest of berry Aegorhinus superciliosus (Coleoptera: Curculionidae). The anti-feeding effects of the extracts on the latter were also evaluated. Residual application was used, with five concentrations for each species of insect and ten replications of each assay. To evaluate anti-fee

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5

TRITTEN, LUCIENNE, OLIVIER BRAISSANT, and JENNIFER KEISER. "Comparison of novel and existing tools for studying drug sensitivity against the hookworm Ancylostoma ceylanicum in vitro." Parasitology 139, no. 3 (2012): 348–57. http://dx.doi.org/10.1017/s0031182011001934.

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SUMMARYThe motility assay is the current gold standard for evaluating drug effects on hookworm larvae and adults, however, among other drawbacks the assay is time consuming, and prone to individual subjectivity. We evaluated six alternative in vitro assays, namely the feeding inhibition assay, the colourimetric AlamarBlue®, MTT formazan and acid phosphatase activity assays, as well as isothermal calorimetry and the xCELLigence System using Ancylostoma ceylanicum third-stage larvae, stimulated third-stage larvae and adults. The performances of the assays were compared to the motility assay usin

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6

Klingeman, William E. "Bagworm Survival and Feeding Preferences as Indicators of Resistance among Maples." Journal of Environmental Horticulture 20, no. 3 (2002): 138–42. http://dx.doi.org/10.24266/0738-2898-20.3.138.

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Abstract The bagworm (Thyridopteryx ephemeraeformis (Haworth)) is a polyphagous, native pest of numerous deciduous and evergreen ornamental plants. Bagworm larvae were used to investigate host plant susceptibility among ten species and cultivars of maples that are economically important and commonly encountered in landscapes in the eastern United States. Data analyses from 48-hour choice assays, conducted in the laboratory during 2000 and 2001, indicated that differences existed among maples for bagworm feeding preferences and host plant susceptibility. Results from the 48-hour trials were not

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7

Tanne, E., E. Boudon-Padieu, D. Clair, M. Davidovich, S. Melamed, and Meir Klein. "Detection of Phytoplasma by Polymerase Chain Reaction of Insect Feeding Medium and Its Use in Determining Vectoring Ability." Phytopathology® 91, no. 8 (2001): 741–46. http://dx.doi.org/10.1094/phyto.2001.91.8.741.

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A polymerase chain reaction (PCR)-based method was developed for the detection of phytoplasma in insect feeding medium (sucrose). A correlation was established between the transmissibility of Flavescence dorée phytoplasma in the experimental leafhopper vector Euscelidius variegatus and its detection by PCR in the insect feeding medium. However, phytoplasma were detected in the insects' bodies 3 weeks before they began to transmit. Hence, PCR assays of the sucrose medium reflected phytoplasma vectoring ability probably by detecting it in the insect saliva, whereas detection of phytoplasma in th

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8

Grace, J. Kenneth. "Oral Toxicity of Barium Metaborate to the Eastern Subterranean Termite (Isoptera: Rhinotermitidae)." Journal of Entomological Science 25, no. 1 (1990): 112–16. http://dx.doi.org/10.18474/0749-8004-25.1.112.

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The oral toxicity of barium metaborate monohydrate (Busan 11-Ml) to Reticulitermes flavipes (Kollar) was evaluated in no-choice assays by feeding termite workers for 15 and 30 days on filter papers treated with concentrations of 500–40,000 ppm (weight/weight). In the 15 day assay, 30,000 ppm resulted in 92 ± 17% termite mortality and a concomitant 86% reduction in paper consumption. Feeding for 30 days on 1,500 ppm resulted in 100% mortality. Reduced paper consumption was associated with termite mortality, and feeding on low concentrations did not differ from that on control papers. Concentrat

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9

Lait, Cameron G., Daniel R. Miller, Sarah L. Bates, John H. Borden, and Allison R. Kermode. "Biochemical Assay Detects Feeding Damage to Loblolly Pine Seeds Caused by the Leaffooted Pine Seed Bug (Hemiptera: Coreidae)." Journal of Entomological Science 38, no. 4 (2003): 644–53. http://dx.doi.org/10.18474/0749-8004-38.4.644.

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A large number of proteins in salivary gland extracts of the leaffooted pine seed bug, Leptoglossus corculus Say, were strongly recognized by a polyclonal antibody-based assay developed for detecting saliva of the western conifer seed bug. Leptoglossus occidentalis Heidemann, in lodgepole pine, Pinus contorta var. latifolia Engelmann, seeds. An average of approximately 85% of loblolly pine, Pinus taeda L., seeds exposed to feeding by L. corculus for 1 to 4 weeks in the laboratory contained detectable amounts of salivary proteins when the antibody assays were performed weekly on samples (n = 10

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10

Bhaskar Gollapudi, B., Rebekah J. Bruce, and Anil K. Sinha. "The role of feeding rejection in Drosophila mutation assays." Mutation Research Letters 144, no. 1 (1985): 13–17. http://dx.doi.org/10.1016/0165-7992(85)90117-4.

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