119 research outputs found

    Trophic Interactions Between Two Herbivorous Insects, \u3cem\u3eGalerucella calmariensis\u3c/em\u3e and \u3cem\u3eMyzus lythri\u3c/em\u3e, Feeding on Purple Loosestrife, \u3cem\u3eLythrum salicaria\u3c/em\u3e, and Two Insect Predators, \u3cem\u3eHarmonia axyridis\u3c/em\u3e and \u3cem\u3eChrysoperla carnea\u3c/em\u3e

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    The effects of two herbivorous insects, Galerucella calmariensis Duftschmid and Myzus lythri L. (Coleoptera: Chrysomelidae), feeding on purple loosestrife, Lythrum salicaria L. (Myrtiflorae: Lythraceae), were measured in the presence of two insect predators, Harmonia axyridis Pallas (Coleoptera: Coccinellidae) and Chrysoperla carnea (Stephens) (Neuroptera: Chrysopidae). A greenhouse cage experiment examined the direct effects of these predators on these herbivores, and indirect effects of predation on aboveground biomass, defoliation, number of leaves, and internode length. Eight treatment combinations with G. calmariensis, M. lythri, H. axyridis and C. carnea were applied to caged L. salicaria. The experiment ended when G. calmariensis adults were observed, 11 to 13 days after release of first instar G. calmariensis. G. calmariensis larvae alone removed significant amounts of leaf tissue and reduced the number of L. salicaria leaves. Predators did not reduce levels of defoliation by G. calmariensis. C. carnea had no effect on G. calmariensis survival, but H. axyridis reduced G. calmariensis survival in the presence of M. lythri. Both predators reduced the survival of M. lythri. This short duration greenhouse study did not demonstrate that predator-prey interactions altered herbivore effects on L. salicaria

    Trophic Interactions Between Two Herbivorous Insects, Galerucella calmariensis and Myzus lythri, Feeding on Purple Loosestrife, Lythrum salicaria, and Two Insect Predators, Harmonia axyridis and Chrysoperla carnea

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    The effects of two herbivorous insects, Galerucella calmariensis Duftschmid and Myzus lythri L. (Coleoptera: Chrysomelidae), feeding on purple loosestrife, Lythrum salicaria L. (Myrtiflorae: Lythraceae), were measured in the presence of two insect predators, Harmonia axyridis Pallas (Coleoptera: Coccinellidae) and Chrysoperla carnea (Stephens) (Neuroptera: Chrysopidae). A greenhouse cage experiment examined the direct effects of these predators on these herbivores, and indirect effects of predation on aboveground biomass, defoliation, number of leaves, and internode length. Eight treatment combinations with G. calmariensis, M. lythri, H. axyridis and C. carnea were applied to caged L. salicaria. The experiment ended when G. calmariensis adults were observed, 11 to 13 days after release of first instar G. calmariensis. G. calmariensis larvae alone removed significant amounts of leaf tissue and reduced the number of L. salicaria leaves. Predators did not reduce levels of defoliation by G. calmariensis. C. carnea had no effect on G. calmariensis survival, but H. axyridis reduced G. calmariensis survival in the presence of M. lythri. Both predators reduced the survival of M. lythri. This short duration greenhouse study did not demonstrate that predator-prey interactions altered herbivore effects on L. salicaria

    Purple Loosestrife: History, Management, and Biological Control in Iowa

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    Purple loosestrife (Lythrum salicaria) is an invasive plant species infesting wetlands in North America. Biodiversity and wetland habitat quality are reduced following purple loosestrife establishment. Several management tactics, including cultural, mechanical, and chemical controls, have had limited success in reducing the spread of purple loosestrife. Beginning in the 1990s, a biological control program has introduced several species of natural enemies from Europe that feed on purple loosestrife. Since 1994, Iowa State University has reared and released two species of beetles that feed on purple loosestrife, Galerucella calmariensis and G. pusilla. Biological control is one component of an integrated purple loosestrife management and education program that is needed to reduce the spread and densities of purple loosestrife

    Quantifying Aphid Predation Rates of Generalist Predators in the Field

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    The community of predators within agroecosystems has the potential to restrict aphid populations, especially early in the season before exponential increases in density and prior to the arrival of specialist natural enemies. Although direct observations of predation, laboratory feeding trials and manipulative field studies have been used to estimate levels of biological control exerted by different species (or potentially negative interactions between them), it is often difficult to extrapolate results to naturally occurring interactions in the field. Over 100 investigations have utilized gut-content analysis to estimate aphid predation rates by predators. Throughout the last century, gut dissection, which enables the visual identification of aphid body parts, has been used in over 50% of studies although accurate identification and quantification of predation is difficult. Other techniques have included radio-labelling of prey, dissection of faecal samples, electrophoresis, stable isotope analysis and use of polyclonal antisera. In recent studies of invertebrate predation, monoclonal antibodies have been the most frequently applied technique but advances in molecular biology have enabled the detection of species-specific DNA sequences. The use of these applications to quantify predation by aphidophagous predators will be reviewed, with emphasis on potential sources of error and difficulties of quantitative interpretation. Despite the considerable focus currently directed towards molecular approaches, antibody-based techniques are likely to remain an important tool for studying predation rates of pests in the field, especially when antibodies have already been developed. However, the study of multiple predation events within complex generalist predator food webs is only likely through the detection of species-specific DNA sequences using molecular techniques
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