Abstract:A synthetic sex pheromone trapping survey of the leaf skeletonizer Uraba lugens Walker (Lepidoptera: Nolidae) demonstrated the unexpectedly widespread distribution of the insect across > 40,000 ha of urban Auckland, New Zealand. A survey of eucalyptus trees planted in parks and other public areas showed a significant spatial correlation between trap catch and breeding populations, validating the trap survey results. Traps in trees showing damage had four-fold higher catches than traps placed in undamaged or no… Show more
“…This species, native to Australia, invaded into New Zealand around 1995 and is now well established in the northern area of New Zealand (Suckling et al, 2005). Some other non-eucalypt tree species including the unrelated Betula pendula Roth (Betulaceae) and Liquidambar have also been identified as 'novel hosts' in New Zealand although being utilized only occasionally (Berndt unpublished data).…”
“…This species, native to Australia, invaded into New Zealand around 1995 and is now well established in the northern area of New Zealand (Suckling et al, 2005). Some other non-eucalypt tree species including the unrelated Betula pendula Roth (Betulaceae) and Liquidambar have also been identified as 'novel hosts' in New Zealand although being utilized only occasionally (Berndt unpublished data).…”
“…An estimate of rates of spread and changes in the distribution range from the initial point of infestation of the non-indigenous insect pest is an essential part of the pest management process. To enable the detection, and to monitor rates of spread, particularly of non-indigenous Lepidopteran pests, pheromone traps have typically been used with a considerable degree of success (Myers & Hosking, 2002;Sharov et al ., 2002;Suckling et al ., 2005;Tobin et al ., 2007). One of the key factors that often influences trap capture rates is the positioning of the trap in the tree canopy (Cardé & Elkinton, 1984).…”
Section: Discussionmentioning
confidence: 99%
“…(2003) note that traps were more efficient at capturing male OPM when placed at this height in the upper canopy, and were less efficient when placed at 2 or 6-8 m. Studies on pine processionary moth (PPM), a close relative of OPM, have also shown that higher numbers of adult males are captured when pheromone traps are placed in the crowns of pine trees (Einhorn et al ., 1983;Jactel et al ., 2006). For many other Lepidoptera species as well, pheromone trap catches are greater when the traps are placed in the upper part of the tree canopy (Sower & Daterman, 1977;Hanula et al ., 1984;Liebhold & Volney, 1984;Bhardwaj & Chander, 1992;Barrett, 1995;Suckling et al ., 2005;Kovanci et al ., 2006). The present study indicated that male OPM captures in traps did not reach a maximum, and continued to rise with an increasing height positioning of the pheromone trap in the canopy.…”
Section: Discussionmentioning
confidence: 99%
“…Pheromone trapping for monitoring populations and dispersal of Lepidopteran pests is a well established technique and has been exploited for use with numerous non-indigenous invasive species worldwide (Sharov et al ., 2002;Myers & Hosking, 2002;Suckling et al ., 2005;Tobin et al ., 2007). It is particularly effective for detecting insect pests at low population densities, although trap captures are influenced by a wide range of factors.…”
1 A field trial conducted in the summer of 2011 evaluated three key parameters that might be influential for determining the number of adult male oak processionary moths (OPM) Thaumetopoea processionea (L.) caught in pheromone traps. Two types of traps (Delta and funnel; Oecos, U.K.) containing one of three different commercially available pheromone lures for OPM were placed out in the lower (3-5 m), mid (5-10 m) and upper (10-15 m) canopy of 72 individual oak trees in Richmond Park, in London, U.K. 2 The traps were placed out for 8 weeks covering the main flight period of OPM, and significantly more male moths were captured in traps positioned in the upper canopy (76.6%) compared with either mid-canopy (18.6%) or lower canopy (4.8%) positions. Funnel traps caught significantly more male OPM than Delta traps, catching almost six times as many moths over the trapping period. 3 Traps containing one of the commercially available pheromone lures did not catch any moths, whereas traps with the other two lures caught similar numbers of moths. Chemical analysis revealed considerable differences between the three pheromone lures used in the trial in terms of the initial starting concentration of the primary component (Z ,Z )-11,13-hexadecadienyl acetate and its dissipation over a 28-day period. 4 The results obtained in the present study indicate some of the main factors that need to be taken into account when using pheromone traps to monitor OPM populations and also contribute to the establishment of a standardized monitoring system for this recently established insect pest.
“…Pheromone baited traps are widely used for biosecurity surveillance to detect new incursions of unwanted organisms, and to delimit their ranges (Augustin et al., 2004; Suckling et al., 2005a,b; Bogich et al., 2008; Liebhold & Tobin, 2008). They have been used for several decades in pest management for monitoring to alert land managers to the presence of a pest in time and space, providing insight into phenology as well as geographic distribution (Suckling et al., 2005b). Pheromone traps have also been used to delimit populations for pest risk modelling (Kriticos et al., 2007).…”
Modelling moth dispersal in relation to wind direction and strength could greatly enhance the role of pheromone traps in biosecurity and pest management applications. Anemotaxis theory, which describes moth behaviour in the presence of a pheromone plume and is used as a framework for such models. Currently, however, that theory includes only three components: upwind, zigzagging, and sideways casting behaviour. We test anemotaxis theory by analysing the data from a series of mark–release–recapture experiments where the wind direction was known and the insects were trapped using an irregular grid of pheromone traps. The trapping results provide evidence of a downwind component to the flight patterns of the released insects. This active or passive downwind dispersal is likely to be an appetitive behaviour, occurring prior to the elicitation of pheromone‐oriented flight patterns (pheromone anemotaxis). Given the potential for significant displacement during downwind dispersal, this component will have impact on final trap captures and should be considered when constructing moth dispersal models.
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