Potential of Colorado Potato Beetle (Coleoptera: Chrysomelidae) to Adapt to Alternative Host Plants.

Twelve selected cultivated or wild solanaceae (Solanum dulcamara, Solanum nigrum, Solanum villosum, Solanum lycopersicum, Solanum muricatum, Solanum melongena, Datura innoxia, Datura metel, Physalis spp., Capsicum annuum, Nicotiana alata, and Petunia spp.) (all species Solanales: Solanaceae) were tested as potential alternative host plants against Solanum tuberosum for a local population of the Colorado potato beetle Leptinotarsa decemlineata Say (CPB) in Estonia. Some CPB populations in America and southern Europe accept most of these plants. However, geographically isolated populations of beetles can differ in their acceptance of new host plants. Migrants from the southern Europe supplement Estonian beetle population regularly, so individuals may differ in their host plant preferences. S. melongena and S. dulcamara were well accepted by the beetles, Lycopersicum spp. (Solanales: Solanaceae) and N. alata were intermediate, and S. villosum and S. nigrum were least accepted. The beetles rejected S. muricatum, Physalis spp., C. annuum, Petunia spp., and D. metel. First-instar larvae completed a full life cycle only on S. dulcamara, N. alata, S. lycopesicum, S. melongena, although their development rate was slower, mortality was higher and emerging adults were underweight relative to those that fed on S. tuberosum. The fourth-instar larvae were less sensitive in relation to food. We found that S. dulcamara as a native plant could provide resources for CPB during early and late season. At the same time, the cultivated S. melongena would be suitable plant species for further testing as dead-end crop for integrated pest management.

Dynamics of Supercooling Ability and Cold Tolerance of the Alder Beetle (Coleoptera: Chrysomelidae).

Agelastica alni L. (Coleoptera: Chrysomelidae) is a common beetle pest of alder trees (Alnus incana L.) in forests and parks across Estonia. The supercooling ability and capacity to survive low temperature exposure changes temporally. Relatively high unimodal supercooling point (SCP) levels (with a mean value of -6 to -8°C) were characteristic of the beetles in September during their diapause induction period, in April when the beetles had terminated their diapause development and in May when they started to reproduce. During their deep diapause period the SCPs of beetles had a bimodal distribution. Some beetles decreased their SCPs to -14 to -19°C while others retained a high SCP value of -6 to -8°C. Most vulnerable to low temperature were overwintered active beetles in May; after 1 h exposure their LTemp50 (median lethal temperature) was -6.3°C. In September with the onset of diapause tolerance of beetles started to increase, LTemp50 = -7.7°C. Beetles were most cold tolerant during their deep diapause period with LTemp50 < -12.0°C. A. alni beetles use one of two different strategies for overwintering, some are freeze-tolerant while others are freeze-avoidant. The freeze-avoidant beetles with low SCP (-12 to -15°C) acquired greater cold tolerance than those with higher SCP (-6 to -8°C), with LTemp50 = -13.7°C and LTemp50 = -11°C, respectively.

The opening-closing rhythms of the subelytral cavity associated with gas exchange patterns in diapausing Colorado potato beetle, Leptinotarsa decemlineata.

The opening-closing rhythms of the subelytral cavity and associated gas exchange patterns were monitored in diapausing Leptinotarsa decemlineata beetles. Measurements were made by means of a flow-through CO2 analyser and a coulometric respirometer. Under the elytra of these beetles there is a more or less tightly enclosed space, the subelytral cavity (SEC). When the cavity was tightly closed, air pressure inside was sub-atmospheric, as a result of oxygen uptake into the tracheae by the beetle. In about half of the beetles, regular opening-closing rhythms of the SEC were observed visually and also recorded; these beetles displayed a discontinuous gas exchange pattern. The SEC opened at the start of the CO2 burst and was immediately closed. On opening, a rapid passive suction inflow of atmospheric air into the SEC occurred, recorded coulometrically as a sharp upward peak. As the CO2 burst lasted beyond the closure of the SEC, we suggest that most of the CO2 was expelled through the mesothoracic spiracles. In the remaining beetles, the SEC was continually semi-open, and cyclic gas exchange was exhibited. The locking mechanisms and structures between the elytra and between the elytra and the body were examined under a stereomicroscope and by means of microphotography. We conclude that at least some of the L. decemlineata diapausing beetles were able to close their subelytral cavity tightly, and that the cavity then served as a water-saving device.

Oxygen convective uptakes in gas exchange cycles in early diapause pupae of Pieris brassicae.

Oxygen convective uptakes in gas exchange cycles were directly recorded in early diapause pupae of Pieris brassicae L. (Lepidoptera; Pieridae) by means of O2 coulometric respirometry. This method was combined with flow-through CO2 respirometry, the two systems being switchable one to the other. During recording with both systems, measurements were also taken with infrared actography. The pupae displayed short discontinuous gas exchange cycles lasting 40-70 min. No true C phase was found by flow-through measurements; instead, flutter opening of the spiracles with discrete convective O2 uptakes began shortly after the O phase whereas CO2 release was suppressed by the inward directed passive suction ventilation. The F phase was characterized by a series of small CO2 bursts (flutter events). Between these bursts, novel sub-phase `miniflutter' was observed, which consisted of six to 10 miniature inspirations without any CO2 emission. During the flow-through measurements, oxygen convective uptakes were indirectly recorded by the infrared actograph as sudden extensions (lengthening) of the abdominal segments at each spiracular microopening.