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Phenacoccus peruvianus (Hemiptera: Pseudococcidae) is an invasive mealybug of Neotropical origin, first reported in the Mediterranean Basin in Almeria (Spain) in 1999. In the following years the mealybug spread into other Mediterranean regions and has also been recorded in Portugal and France, as well as in Sicily, Corsica and the Balearic Islands. Phenacoccus peruvianus is a polyphagous species and damages economically important ornamental plants. Since this was a relatively unknown species, during the first years of invasion, the mealybug was managed by the application of chemical treatments with wide-spectrum pesticides. However, the latest European directive on pesticide use reduces or even forbids pesticide applications in a wide range of urban green areas, giving significant priority to biological control (European Parliament and Council 2009). This thesis sets the basis for introducing biological control into a P. peruvianus management program in urban landscapes, focusing on its characterization, sampling, biology and control. In order to facilitate the identification of this and other mealybug species, we characterised 33 mealybug populations infesting crops and ornamental plants in Eastern Spain, using a combination of molecular and morphological techniques. This characterisation led to the identification of ten mealybug species and made routine identification possible through DNA sequencing or the use of derived species-specific molecular tools. The sequences obtained also add to the phylogenetic knowledge of the Pseudococcidae family and provide insight into the invasion history of some species. Phenacoccus peruvianus populations were high in bougainvillea plants during spring and summer, declining to almost undetectable levels in autumn and winter. The mealybug was mainly found in bracts and there were no significant migrations between plant strata. Phenacoccus peruvianus showed a high aggregated distribution on bracts, leaves and twigs. We recommend a binomial sampling of 200 leaves and an action threshold of 55% infested leaves for IPM purposes in urban landscapes. Its most abundant natural enemies were found to be the primary parasitoids Acerophagus n. sp. near coccois and Leptomastix epona Walker (Hymenoptera: Encyrtidae). We also identified several predator species from the Anthocoridae, Coccinellidae, Chamaemyiidae, and Chrysopidae families. Phenacoccus peruvianus populations were lower during the second and third year of the survey, coinciding with an increase in the parasitoid Acerophagus sp. populations, which displaced the native L. epona. Differential female offspring and resource preemption are discussed as the main reasons for this displacement. To obtain further information on the biology of the new parasitoid Acerophagus sp. we determined some traits of its reproductive and feeding strategies. Acerophagus sp. egg load reached its maximum when it was 5 days old with almost 30 mature eggs. Phenacoccus peruvianus second and third nymphal instars and adults were suitable for parasitism and efficient encapsulation was low (10.76 ± 0.31 %). The parasitoid always preferred older instars when different host instars were available. Acerophagus sp. developed as a solitary parasitoid in the second instar and as a gregarious parasitoid in older instars (2¿4 parasitoids per host). Moreover, it reproduced parthenogenetically and all the emerged offspring were females. Immature development lasted between 20 and 22 days at 25°C and 65% HR. Under these conditions, adults lived for longer than 20 days when fed on honey, but fewer than 3 days when fed on naturally occurring sugar sources (host honeydew and Bougainvillea glabra flowers). / Beltrà Ivars, A. (2014). Biology and management of the invasive mealybug Phenacoccus peruvianus (Hemiptera: Pseudococcidae) in urban landscapes [Tesis doctoral no publicada]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/37233 / TESIS

An established host-parasitoid-hyperparasitoid system was used to investigate how the physiological and behavioural characteristics of parasitoids influence the outcomes of laboratory-based host specificity tests. The characteristics of the two pteromalid egg parasitoids, Enoggera nassaui (Girault) and Neopolycystus insectifurax Girault, were assessed and interpreted in regard to the particular host specificity testing methods used and the control of the eucalypt defoliating beetle Paropsis charybdis Stål (Chrysomelidae) in New Zealand. The physiology of N. insectifurax was examined to determine how to increase production of female parasitoids that were physiologically capable and motivated to parasitise P. charybdis eggs in laboratory trials. Neopolycystus insectifurax were found to be more synovigenic than E. nassaui. Provisioning them with honey and host stimuli for three days, and allowing females to parasitise hosts in isolation (i.e. in the absence of competition) was an effective means of achieving these goals. No-choice tests were conducted in Petri dish arenas with the four paropsine beetles established in New Zealand. All four were found to be within the physiological host ranges of E. nassaui and N. insectifurax, but their quality as hosts, as indicated by the percent parasitised and offspring sex ratios, varied. The results of paired choice tests between three of the four species agreed with those of no-choice tests in most instances. However, the host Trachymela catenata (Chapuis), which was parasitised at very low levels by E. nassaui in no-choice tests, was not accepted by that species in paired choice tests. A much stronger preference by N. insectifurax for P. charybdis over T. catenata was recorded in the paired choice test than expected considering the latter was parasitised at a high level in the no-choice test. The presence of the target host in paired choice tests reduced acceptance of lower ranked hosts. Both no-choice and choice tests failed to predict that eggs of the acacia feeding beetle Dicranosterna semipunctata (Chapuis) would not be within the ecological host range of E. nassaui and N. insectifurax. Behavioural observations were made of interspecific competition between E. nassaui and N. insectifurax for access to P. charybdis eggs. Two very different oviposition strategies were identified. Neopolycystus insectifurax were characterised by taking possession of, and aggressively guarding host eggs during and after oviposition. They also appeared to selectively oviposit into host eggs already parasitised by E. nassaui, but did not emerge from significantly more multi-parasitised hosts than E. nassaui. Enoggera nassaui did not engage in contests and fled when approached by N. insectifurax. Although often prohibited from ovipositing by N. insectifurax, E. nassaui were able to locate and begin ovipositing more quickly, and did not remain to guard eggs after oviposition. It is hypothesised that although N. insectifurax have a competitive advantage in a Petri dish arena, E. nassaui may be able to locate and parasitise more host eggs in the field in New Zealand, where competition for hosts in is relatively low. The biology of the newly established encyrtid Baeoanusia albifunicle Girault was assessed. It was confirmed to be a direct obligate hyperparasitoid able to exploit E. nassaui but not N. insectifurax. Field and database surveys found that all three parasitoids have become established in many climatically different parts of New Zealand. Physiological characteristics were identified that may allow B. albifunicle to reduced effective parasitism of P. charybdis by E. nassaui to below 10%. However, the fact that hyperparasitism still prevents P. charybdis larvae from emerging, and that B. albifunicle does not attack N. insectifurax, may preclude any significant impact on the biological control of P. charybdis. Overall, parasitoid ovigeny and behavioural interactions with other parasitoids were recognised as key characteristics having the potential to influence host acceptance in the laboratory and the successful biological control of P. charybdis in the field. It is recommended that such characteristics be considered in the design and implementation of host specificity tests and might best be assessed by conducting behavioural observations during parasitoid colony maintenance and the earliest stages of host specificity testing.