Soybean HPR virulence and parasitism by Aphelinus
Data files
Apr 28, 2025 version files 16.03 KB
Abstract
Invasions by insect species that become pests are an increasing problem for agriculture. Introductions of parasitoids from the regions of pest origin and breeding plants resistant to invasive pests can reduce invasive pest abundance and impact. Whether interactions between parasitoids and plant resistance are positive or negative depends on the detailed mechanisms. We studied the effects of susceptible versus resistant soybean and avirulent versus virulent soybean aphid on the parasitoids Aphelinus certus and Aphelinus glycinis, the first with a broad host range and the second with a narrow host range. Both parasitoid species parasitized virulent aphids at least as much as avirulent aphids on susceptible and resistant soybeans. Aphelinus certus parasitized fewer avirulent aphids than virulent aphids on resistant soybean and fewer avirulent aphids on resistant versus susceptible soybean. The number of aphids parasitized by A. glycinis did not vary with the treatments. Emergence rates of parasitoid progeny were high for both parasitoids and did not vary with the treatments. Progeny sex ratios of the parasitoids did not vary with plant resistance or aphid virulence. However, for A. certus, there was a small effect of the interaction between plant resistance and aphid virulence. Body masses of female and male progeny of A. certus did not vary with the treatments. However, body masses of female progeny of A. glycinis were larger on susceptible versus resistant soybeans and on virulent versus avirulent aphids. Body masses of male progeny of A. glycinis were larger on susceptible versus resistant plants. Parasitism by A. certus is known to be density-dependent, and given that density-dependent parasitism has been found in several other species of Aphelinus, parasitism by A. glycines is very likely also to be density-dependent. Given the higher densities of virulent versus avirulent aphids on resistant soybean reported in the literature, these parasitoids should parasitize more virulent than avirulent aphids on resistant soybean and would limit the abundance of virulent soybean aphid if much of the soybean acreage had resistant plants. Little research has been published previously on the combined impacts of plant resistance and herbivore virulence on parasitoids. If our results hold true in other systems, plant resistance and biological control may be more compatible in suppressing herbivore virulence than has sometimes been proposed.
Dataset DOI: 10.5061/dryad.0cfxpnwch
Description of the data and file structure
DATA DESCRIPTION
We tested the effects of plant resistance and aphid virulence on the numbers of aphids parasitized, as well as parasitoid emergence, sex ratio, and body mass of females and males in randomized complete-block experiments separately for the two species of parasitoids. The experimental unit was a potted plant covered with a cage (10x22cm) and infested with 100 mixed-instar aphids. There were 48 units planted with susceptible soybeans and 48 planted with resistant soybeans. For each level of resistance, 24 units were infested with avirulent aphids and 24 were infested with virulent aphids, for a total of 96 experimental units. Among the experimental units, 40 were exposed to one parasitoid species, and 40 to the other parasitoid species. We added a single, female parasitoid, previously exposed to males, a day after aphid infestation, and we removed the female a day later. After two weeks, we harvested the plants and later counted the number of mummified aphids and the numbers and genders of adult parasitoid progeny. We weighed the parasitoid progeny to get mean body masses for each experimental unit with parasitoids. Because females of many parasitoid species are larger than males, we weighed females and males separately and analyzed the effects of the treatments on the masses of females and males separately. We calculated progeny emergence rates for experimental units with at least four mummified aphids, which reduced replication from 40 experimental units for each parasitoid species to 20 for A. certus and 21 for A. glycinis.
| variable | definition |
|---|---|
| wasp_species | species of parasitoid |
| country | collection country |
| city | collection city |
| site | collection site |
| year | collection year |
| biotype | Aphis glycines virulence biotype (1 = avirulent; 4 = virulent) |
| wasp_id | parasitoid indicator |
| wasp_pop | parasitoid subpopulation |
| soybean_accession | soybean accession indicator |
| alleles | resistance alleles |
| block | randomization block |
| location | location within randomization block |
| date_in | date parasitoids added aphid cage |
| time_in | date parasitoids added aphid cage |
| date_out | date parasitoids added aphid cage |
| time_out | date parasitoids added aphid cage |
| wasp_fate | whether the parasitoid was live, dead, or missing when removed from the aphid cage |
| plant_fate | whether the plant was live or dead when the mummies were harvested |
| n_mum | number of mummified aphids |
| n_emer | number of mummified aphids from which parasitoids emergec |
| n_adult | number of adult parasitoid progeny |
| n_males | number of adult male parasitoid progeny |
| n_males_weighed | number of males weighed |
| weight_males | weight of males (micrograms of dry mass) |
| n_females | number of adult female parasitoid progeny |
| n_females_weighed | number of females weighed |
| weight_females | weight of females (micrograms of dry mass) |
Access information
NA
