31 research outputs found

    Below ground efficiency of a parasitic wasp for Drosophila suzukii biocontrol in different soil types

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    The parasitoid wasp Trichopria drosophilae is promising as a biocontrol agent for controlling the ubiquitous pest Drosophila suzukii (Matsumura). Crucial for the successful implementation of any biocontrol agent is a high parasitisation rate by the parasitoid. Most studies investigating the parasitisation rate of D. suzukii pupae have focused on parasitisation in the fruit or in a petri dish. However, the predominant pupation site of D. suzukii in the field is the soil. Unfortunately, little is known on how well parasitoid wasps can detect and parasitise pupae of D. suzukii buried in the soil. Therefore, we conducted soil parasitisation experiments of T. drosophilae on D. suzukii pupae using two pupation depths in three different soil types (loamy sand, loam, and clay). In all three soil types, we found generally low D. suzukii pupae parasitisation rate by T. drosophilae, independent of the pupation depth. The pupation behaviour of D. suzukii and the parasitisation behaviour of T. drosophilae are discussed in detail. For pest control in most soil types, our results mean that the number of D. suzukii larvae pupating in the soil should be reduced, e.g., by adding a layer of sandy soil or covering the soil with plastic mulch. This might increase the probability of success when using T. drosophilae as a biocontrol agent

    The role of pollinator attracting scent in the sexually deceptive orchids Ophrys chestermanii, O. normanii and O. tenthredinifera

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    Sexual deception of male bees is one of the most remarkable mechanisms of pollination (Ackermann 1986, Proctor & al. 1996). Flowers of the orchid genus Ophrys mimic females of their pollinator species, usually bees and wasps, to attract males, which try to copulate with the flowers. During this so-called “pseudocopulation” the male removes the pollinia and transfers them to another flower to ensure pollination. Apart from visual and tactile cues, floral scent was shown to be most important for eliciting mating behaviour in males (Kullenberg 1961, Schiestl & al. 1999, Ayasse & al. 2003). Pollination in Ophrys is highly specific and usually each Ophrys species attracts only one pollinator species (Paulus & Gack 1990). The high degree of specialization provides the means of reproductive isolation between the intercrossable Ophrys-species (Ehrendorfer 1980). The complex odour-bouquets released by the flowers are species-specific and often consist of more than 100 different chemical compounds (Borg-Karlson & al. 1985, Ayasse 2006). Speciation in Ophrys-orchids may be brought about by changes in the pollinator attracting floral scent. The attraction of a new pollinator may act as a pre-zygotic isolation barrier (Stebbins 1970, Paulus & Gack 1990, Soliva & al. 2001). We investigated three sympatrically occuring Ophrys-species on Sardinia. O. chestermanii and O. normanii are endemic and are both pollinated by males of the bumblebee B. vestalis. O. tenthredinifera is pollinated by Eucera nigrilabris. There are different opinions concerning the taxonomic status of O. normanii. It has been described as an actual hybrid between O. chestermanii and O. tenthredinifera (Wood 1983). Paulus & Gack (1995) suggested that it is an own species, that either has developed from a hybrid between O. chestermanii and O. normanii or that has evolved by radiation from O. tenthredinifera. By conducting behavioural-tests with B. vestalis males, performing gas chromatographic analyses and electrophysiological studies we wanted to identify pollinator attracting scent and to clarify the taxonomic status of O. normanii.SexualtĂ€uschorchideen der Gattung Ophrys (Orchidaceae) imitieren die Weibchen ihrer BestĂ€uber in Duft, Form und Farbe. InsektenmĂ€nnchen versuchen mit dem Labellum der BlĂŒte zu kopulieren und transportieren den Pollen von BlĂŒte zu BlĂŒte, wodurch die Orchidee bestĂ€ubt wird. In dieser Arbeit untersuchten wir die BestĂ€uber anlockenden Duftstoffe der beiden endemisch auf Sardinien vorkommenden Arten O. normanii und O. chestermanii, die beide von Bombus vestalis MĂ€nnchen (Hymenoptera: Apidae) bestĂ€ubt werden und von O. tenthredinifera, die Eucera nigrilabris (Hymenoptera: Apidae) zur BestĂ€ubung anlockt. O. normanii wurde von Wood (1983) als PrimĂ€rhybride beschrieben. Nach Paulus und Gack (1995) handelt es sich um eine hybridogene Art oder um eine Art die durch Abspaltung von O. tenthredinifera entstanden ist. Das Ziel der Untersuchungen war die Identifizierung MĂ€nnchen-anlockender Verbindungen. Die AttraktivitĂ€t der drei Arten fĂŒr B. vestalis MĂ€nnchen sollte Hinweise auf den Artstatus von O. normanii geben. In Biotests mit B. vestalis-MĂ€nnchen lösten BlĂŒtenextrakte von O. normanii und O. chestermanii ebenso wie B. vestalis-Weibchen Kopulationsverhalten der MĂ€nnchen aus, nicht jedoch Extrakte von O. tenthredinifera. Folglich handelt es sich bei O. normanii nicht um einen aktuellen Hybriden zwischen O. chestermanii und O. tenthredinifera. Ein Vergleich der GC-EAD-aktiven Duftbouquets mittels Diskriminanzanalyse ergab große Ähnlichkeiten zwischen O. normanii und O. chestermanii fĂŒr die Substanzklassen der Ester, Alkohole und FettsĂ€uren, die daher vermutlich eine SchlĂŒsselfunktion bei der BestĂ€uberanlockung haben

    Pollinator driven radiation in sexually deceptive orchids of the genus Ophrys

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    Reproductive isolation of sexually deceptive orchid species of the genus Ophrys is based on the specific attraction of a single pollinator species by mimicking the female sex-pheromone of its pollinator. The attraction of a new pollinator caused by changes in the flower odour by drift or hybridization could lead to sympatric speciation. I investigated putative hybrid swarms of Ophrys on Sardinia and Majorca using behavioural experiments, electrophysiology, chemical analysis, and molecular markers (AFLP). On Sardinia I investigated hybrid swarms between O. lupercalis and O. iricolor. In behavioural experiments I found cross attraction of pollinators between species, as well as flowers that were attractive to both pollinators. The analysis of the EAD-active odour compounds showed a significant difference in the flower odour between both parental species, but with a huge overlap between species. AFLP data of the same plant specimen clearly showed the hybridization between O. lupercalis and O. iricolor. A different situation was found on Majorca, where O. lupercalis, O. bilunulata, and O. fabrella bloom consecutively. In the genetic analyses O. bilunulata did not form a distinct group, due to hybridization with both other species. In contrast to this, the analysis of flower odour shows a distinct odour for each species. My results show that reproductive isolation in Ophrys is not as complete as thought so far and that pollinator shifts may have played an important role in the evolution of this group

    Morphology and ultrastructure of the allomone and sex-pheromone producing mandibular gland of the parasitoid wasp Leptopilina heterotoma (Hymenoptera: Figitidae)

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    Chemical communication by the parasitoid wasp Leptopilina heterotoma is based largely on (-)-iridomyrmecin. The female wasps use (-)-iridomyrmecin as a defensive allomone, a chemical cue to avoid competition with con- and heterospecific females, and as a major component of their sex pheromone to attract males. Males of L heterotoma produce (+)-isoiridomyrmecin, which is also used for chemical defense. In this study we show that females and males of L. heterotoma produce the iridomyrmecins in a pair of mandibular glands. Each gland consists of a secretory part composed of class 3 gland cells and their accompanying duct cells, as well as a reservoir bordered by a thin intima. The gland discharges between the mandible base and the clypeus. Males have considerably smaller glands than females, which corresponds to the lower amount of iridomyrmecins produced by males. Chemical analyses of the mandibular gland contents showed that the gland of females contained mainly (-)-iridomyrmecin, as well as low amounts of the other previously described iridoid pheromone compounds, while the glands of males contained only (+)-isoiridomyrmecin. The morphology and sizes of the mandibular glands of males and females of L. heterotoma have evolved to the multi-functional use of iridomyrmecin. (C) 2016 Elsevier Ltd. All rights reserved

    Interference of chemical defence and sexual communication can shape the evolution of chemical signals

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    Abstract According to current evolutionary theory, insect pheromones can originate from extant precursor compounds being selected for information transfer. This is exemplified by females of the parasitoid wasp Leptopilina heterotoma whose defensive secretion consisting mainly of (−)-iridomyrmecin has evolved secondary functions as cue to avoid other females during host search and as female sex pheromone. To promote our understanding of pheromone evolution from defensive secretions we studied the chemical ecology of Leptopilina clavipes. We show here that L. clavipes also produces a defensive secretion that contains (−)-iridomyrmecin as major component and that females use it to detect and avoid host patches occupied by other females. However, the female sex pheromone of L. clavipes consists solely of cuticular hydrocarbons (CHCs) and males did not respond to female CHCs if presented in combination with the defensive secretion containing (−)-iridomyrmecin. This is in contrast to other species of Leptopilina, in which the iridoid compounds have no inhibiting effect or even function as sex pheromone triggering courtship behaviour. This indicates that Leptopilina species differ in the cost-benefit ratio for males searching for females, which might explain the strong divergence in the composition of the sex pheromone in the genus
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