The effect of temperature on host patch exploitation by an egg parasitoid

The effect of temperature during host patch exploitation by parasitoids remains poorly understood, despite its importance on female reproductive success. Under laboratory conditions, we explored the behaviour of Anaphes listronoti, an egg parasitoid of the carrot weevil, Listronotus oregonensis, when foraging on a host patch at five temperatures. Temperature had a strong effect on the female tendency to exploit the patch: A. listronoti females parasitized more eggs at intermediate temperature (20 to 30°C) compared to those foraging at the extreme of the range (15.9°C and 32.8°C). However, there was no difference in offspring sex-ratio and clutch size between temperature treatments. Mechanisms of host acceptance within a patch differed between temperatures, especially at 32.8°C where females used ovipositor insertion rather than antennal contact to assess whether a host was already parasitized or not, suggesting that host handling and chemical cues detection were probably constrained at high temperature. Females spent less time on the host patch with increasing temperatures, but temperature had no effect on patch-leaving rules. Our results show that foraging A. listronoti females behave better than expected at sub-optimal temperatures, but worse than expected at supra-optimal temperatures. This could impair parasitoid performance under ongoing climate change.

Degree-day models to predict carrot weevil (Coleoptera: Curculionidae) emergence and oviposition in Nova Scotia, Canada

Carrot weevil, Listronotus oregonensis (LeConte) (Coleoptera: Curculionidae), is a pest of carrot (Daucus carota var. sativus Hoffmann; Apiaceae) throughout eastern Canada. Carrot weevil emergence and oviposition were monitored in commercial carrot fields in Nova Scotia. Cumulative degree days were calculated using a base temperature of 7 °C (DD7), and models were developed to predict cumulative emergence and oviposition using nonlinear regression. Cumulative emergence and oviposition were adequately explained as functions of DD7 by a three-parameter sigmoidal Hill equation. Our emergence model predicted initial and peak adult emergence at 35 and 387 DD7, respectively, with oviposition on carrot baits occurring as early as 42 DD7. Models were then validated to evaluate how well they performed. Oviposition on carrot plants began at the fourth true-leaf stage (342 DD7) and continued until eleventh true-leaf stage. Growers using these models can identify their window of opportunity to manage their carrot weevil populations targeting the majority of emerged adults before oviposition begins in the field.

Prevalence of a nematode castrator of the carrot weevil and impact on fecundity and survival

Bradynema listronoti is a parasitic nematode described from infected specimens of the carrot weevil Listronotus oregonensis. Prevalence of infection by B. listronoti under field conditions was followed over a period of 16 years in an untreated carrot field. Susceptibility of different carrot weevil life stages was evaluated as well as the impact of infection on fecundity and mortality. Gene expression in infected and uninfected carrot weevils was also compared to evaluate the impact of the parasite on the host transcriptome. Prevalence of B. listronoti in carrot weevil populations was sustained over the years ranging from 20 to 63%. All the weevil stages exposed to B. listronoti inoculum were susceptible to infection, larvae being more vulnerable (59 ± 8% infected) compared with pupae (4 ± 3% infected) and adults (7 ± 3% infected). The fecundity of infected female weevils was greatly reduced (60-fold) due to an inhibition of the maturation of the reproductive system. Transcriptomic analyses revealed that this parasitic castration may have been triggered by the inhibition of reproductive hormone production. The B. listronoti–L. oregonensis interaction represents a case of parasitic castration with a unique potential for biological control of an important pest of carrots.

Population variability of a native and an introduced herbivore of carrots (Apiaceae)

Long-term, twice weekly, trap catches of the native carrot weevil, Listronotus oregonensis (LeConte) (Coleoptera: Curculionidae), and the introduced carrot rust fly, Psila rosae (Fabricius) (Diptera: Psilidae), were used to test the hypothesis that native populations fluctuate less from year-to-year than those of introduced species, because the native species has had more time to adapt to temporal variability in its habitat than an introduced species. Variability in annual abundance was estimated for 33 years, and for 11-year or 16–17-year subsets of the 33-year time series. Temporal population variability was quantified as PV, a proportion between 0 and 1. The native carrot weevil had a PV of 0.39, less than that of the introduced carrot rust fly with a PV of 0.67, supporting the hypothesis. Generation 1 for both species showed a decline in PV over three decades consistent with the hypothesis that adaptation to variability in the habitat leads to lower PV. Over 33 years, the carrot weevil developed a second generation with a PV of 0.70, higher than that of the first generation, which is consistent with the hypothesis that adaptation is required to stabilise population dynamics in a new habitat, in this case a new temporally defined habitat.

NAnnotated checklist of the tribe Listroderini (Coleoptera: Curculionidae: Cyclominae)

The weevil tribe Listroderini (Curculionidae: Cyclominae) was originally recognized for a group of New World taxa. During the last decades its concept was expanded, and additional new taxa were described from the Americas, Australia, New Zealand, and the Tristan da Cunha-Gough islands. This checklist evaluates the nomenclatural status of all the generic and specific names applied to listroderines. A total of 407 species classified into 36 genera are recognized. The following synonymies are established: Gromilus insularis robustus Brookes, 1951 and G. insularis antipodarum Kuschel, 1964 = G. insularis Blanchard, 1853; Gromilus veneris setarius Broun, 1909 = G. veneris (Kirsch, 1877); and Listronotus oregonensis tessellatus Casey, 1895 = L. oregonensis (LeConte, 1876). Two secondary homonyms were detected and replacement names are proposed: Gromilus brounii for G. setosus (Broun, 1917 non Broun, 1893), and Gromilus kuschelii for G. striatus (Broun, 1921 non Broun, 1915).