Ludovic Giuge

INVADING PARASITOIDS SUFFER NO ALLEE EFFECT: A MANIPULATIVE FIELD EXPERIMENT

One frequent explanation for the failure of biological invasions is the Allee effect: due to positive density dependence, initially small invading populations may fail to establish and spread. Populations released for biological control are similar to fortuitous invading populations and may therefore suffer from Allee effects. However, unlike fortuitous invasions, biological control allows the experimental manipulation of initial population size and, thus, offers a unique opportunity to test for the occurrence of Allee effects. We manipulated the initial size of 45 populations of a parasitoid wasp introduced for the biological control of a phytophagous insect and followed the population dynamics of both parasitoids and hosts during three years. Our results suggest an absence of Allee effects but clear negative density dependence instead: (1) the probability of establishment after three years was not affected by initial population size; (2) net reproductive rate was highest at low parasitoid density and high host density; (3) the sex ratio, reflecting the proportion of virgin females, did not increase at low density, suggesting that low densities did not impede mate-finding; (4) the depression of host populations did not depend upon the number of parasitoids introduced. This is, to our knowledge, the first experimental test of the Allee effect in an invading parasitoid. It leads us to propose that a number of behavioral and life-history features of many parasitoids could protect them from Allee effects.

A natural flightless mutation in the ladybird, Harmonia axyridis

A homozygous flightless strain, obtained by selection from a laboratory population of Harmonia axyridis Pallas (Coleoptera, Coccinellidae), has been reared under controlled conditions since 1982 after sampling in China. The adults of this flightless strain have normal elytra and wings but drop almost vertically when they attempt to fly. The origin of this mutation, whether laboratory or natural, is discussed. As the mutation does not affect the fitness of the beetles, this flightless strain can be used in biological control. Releasing flightless adults rather than larvae should provide the potential for more continuous control of aphids by both larvae and adults.

Locomotory behavior of flightless Harmonia axyridis Pallas (Col., Coccinellidae).

To improve the efficiency of the lady beetle H. axyridis as a biological control agent against aphids, a flightless population was obtained by feeding adults with a mutagen and selecting their progeny for nonflying but otherwise morphologically normal individuals. These flightless adults attempted to fly but immediately fell. They softened their fall by opening their elytrae and wings. The inability to fly could result from change in their flying behavior compared to control adults. The flight duration was very much shorter, and the wing beat frequency and, more particularly, the amplitude of the wing beats were clearly lower. More time was spent in the other components of the flight behavior such as wing rotation, wing immobility, and wing folding. The sequence of these patterns differed slightly, due mainly to change in their frequency. The locomotor behavior was not modified by the mutation, which affected only the wing muscles. Searching behavior of mutant adults differed from that of control adults only in that they took longer to encounter and ingest aphids. Nevertheless, the larval growth and reproductive rate remained unchanged. The behavioral and biological features of these flightless adults indicate that it should be possible to use them in biological control programs.

RETRACTED: Locomotory behavior of flightless Harmonia axyridis Pallas (Col., Coccinellidae)

To improve the efficiency of the ladybeetle Harmonia axyridis as a biological control agent against aphids, a flightless population was produced by feeding adults with a mutagen and selecting their progeny for non-flying but otherwise morphologically normal individuals. The inability to fly could result from a change in their flying behavior compared with control adults. Flight duration was very much shorter, wing beat frequency and more particularly the amplitude of the wing beats were clearly lower. More time was spent on the other components of flight behavior such as wing rotation, wing immobility and wing folding. The sequence of these patterns differed slightly mainly due to changes in their frequency. The locomotory behavior was not modified by the mutation, which only affected the wing muscles. The searching behavior of mutant adults differed from that of control adults only in that they took longer to encounter and ingest aphids. As this difference is not important, it should be possible to use this flightless population in biological control programs.