Abstract:Predation rate and numerical response are basic to any investigation of predatorprey relationships and key components in the selection of predators for biological control. The density-dependent predation rate and numerical response of Aphidoletes aphidimyza (Rondani) (Diptera: Cecidomyiidae) to varying densities (5, 10, 20, 40, 60 and 80) of third-instar Aphis craccivora (Koch) (Hemiptera: Aphididae), were studied in laboratory conditions [23±1°C, 70 ± 5% relative humidity (RH), and a photoperiod of 16:8 h L:D… Show more
“…First, the effects of plant traits on A. aphidimyza larval performance may be exacerbated under more variable field conditions compared with those in the laboratory. Second, A. aphidimyza is known to vary its clutch size in response to aphid density in the field (Sentis et al ., ) and the laboratory (Lucas & Brodeur, ; Madahi et al ., ), but the effect of aphid density on oviposition is much stronger on patches near plant meristems (Jandricic et al ., ). Although cumulative aphid days was not retained in our model (but see Appendix S1), cumulative leaf days did significantly predict predatory fly abundance in our field study.…”
1. Although preference-performance relationships in insects are typically studied in a bi-trophic context, it is well known that host plants can affect both the preference and performance of natural enemies of herbivorous insects.2. This study presents evidence from field and laboratory studies that two species of milkweeds, the putatively less defended Asclepias incarnata and the putatively more defended Asclepias syriaca, differentially affect adult oviposition and larval performance in Aphidoletes aphidimyza, an aphid-feeding predatory midge, independent of aphid density.3. Host plant species affected predatory fly larvae abundance by a factor of 50 in the field and a factor of 8 in the laboratory. Larval and adult emergence rates in our laboratory studies provided strong evidence for reduced performance on A. syriaca. Oviposition in choice and no-choice settings provided some evidence for preference for A. incarnata, and a potentially suppressive effect of A. syriaca.4. The results provide limited support for the hypothesis that natural selection can lead to positive correlations between adult oviposition preferences and larval performance upon various food sources, even when predatory insects oviposit onto host plants of their herbivorous prey.5. Preference and performance are not perfectly aligned in this system, however, because ovipositing females do not reject A. syriaca entirely. Potential explanations for mismatches between preference and performance in this system include the neural constraints associated with being a generalist, adaptive time-limited foraging strategies, and unique evolutionary histories of laboratory colonies compared with wild insects.
“…First, the effects of plant traits on A. aphidimyza larval performance may be exacerbated under more variable field conditions compared with those in the laboratory. Second, A. aphidimyza is known to vary its clutch size in response to aphid density in the field (Sentis et al ., ) and the laboratory (Lucas & Brodeur, ; Madahi et al ., ), but the effect of aphid density on oviposition is much stronger on patches near plant meristems (Jandricic et al ., ). Although cumulative aphid days was not retained in our model (but see Appendix S1), cumulative leaf days did significantly predict predatory fly abundance in our field study.…”
1. Although preference-performance relationships in insects are typically studied in a bi-trophic context, it is well known that host plants can affect both the preference and performance of natural enemies of herbivorous insects.2. This study presents evidence from field and laboratory studies that two species of milkweeds, the putatively less defended Asclepias incarnata and the putatively more defended Asclepias syriaca, differentially affect adult oviposition and larval performance in Aphidoletes aphidimyza, an aphid-feeding predatory midge, independent of aphid density.3. Host plant species affected predatory fly larvae abundance by a factor of 50 in the field and a factor of 8 in the laboratory. Larval and adult emergence rates in our laboratory studies provided strong evidence for reduced performance on A. syriaca. Oviposition in choice and no-choice settings provided some evidence for preference for A. incarnata, and a potentially suppressive effect of A. syriaca.4. The results provide limited support for the hypothesis that natural selection can lead to positive correlations between adult oviposition preferences and larval performance upon various food sources, even when predatory insects oviposit onto host plants of their herbivorous prey.5. Preference and performance are not perfectly aligned in this system, however, because ovipositing females do not reject A. syriaca entirely. Potential explanations for mismatches between preference and performance in this system include the neural constraints associated with being a generalist, adaptive time-limited foraging strategies, and unique evolutionary histories of laboratory colonies compared with wild insects.
“…Aphidoletes aphidimyza Rondani (Diptera: Cecidomyiidae) is widely used to control aphids in agricultural systems 13 . It is an oligophagous insect that displays remarkable voracity and targets more than 80 species of aphids, including the major pests, namely Aphis craccivora 14 , Aphis gossypii 15 , Myzus persicae 16 , and others 17 . Owing to the limited dispersal ability of larvae, adults primarily depend on oviposition near aphid colonies to facilitate the predation of their progeny and the establishment of their population 13 , 18 – 20 .…”
Aphidoletes aphidimyza is widely recognized as an effective predator of aphids in agricultural systems. However, there is limited understanding of its predation mechanisms. In this study, we generated a high-quality chromosome level of the A. aphidimyza genome by combining PacBio, Illumina, and Hi-C data. The genome has a size of 192.08 Mb, with a scaffold N50 size of 46.85 Mb, and 99.08% (190.35 Mb) of the assembly is located on four chromosomes. The BUSCO analysis of our assembly indicates a completeness of 97.8% (n = 1,367), including 1,307 (95.6%) single-copy BUSCOs and 30 (2.2%) duplicated BUSCOs. Additionally, we annotated a total of 13,073 protein-coding genes, 18.43% (35.40 Mb) repetitive elements, and 376 non-coding RNAs. Our study is the first time to report the chromosome-scale genome for the species of A. aphidimyza. It provides a valuable genomic resource for the molecular study of A. aphidimyza.
“…The numerical response of insect predators is modelled by assuming that the daily oviposition rate of adult females increases with their daily predation rate (Crawley, 1975). This is approximated using a linear relationshipevery prey eaten results in a constant increase in the predator's daily oviposition rate up to a maximum value (prey required for satiation) (Crawley, 1975;Rahman et al, 2012;Madahi et al, 2015;Nasreen et al, 2021;Loko et al, 2022). Hence, the daily oviposition rate (eggs/female/day) of an adult Orius female (e o a ) is formulated as…”
Section: The Relationship Between Predator Oviposition Rate and The N...mentioning
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