The physiological age of adult males of seven mealybug species was measured in relation to the elongation of the male pair of the waxy caudal filaments. These filaments begin to emerge after eclosion and reached their maximum length from 29.4–46.6 h. The studied males were divided into three age groups, expressed as percentages of the total waxy caudal filaments length. Attraction to a sex pheromone source was significantly higher in the oldest male group (maximum filaments growth) compared with youngest one. Only the oldest male group copulated successfully; few of the younger males tested displayed 'courtship' behavior towards conspecific virgin females. The calculated duration of the sexually active phase of the adult male life cycle varied among species ranging from 34.4 to 46.6 h. There were marked variations in the strength of attraction to a pheromone source according to time of day. There was a continuous decrease in sexual activity from morning to evening. Our findings reveal clear maturation periods for adult males of the seven studied species. The long immature phase of the adult male mealybug is probably also related to several physiological processes that are needed to complete male maturation. The most noticeable change is the elongation of the waxy caudal filaments. However, mating may be performed at any time ambient conditions are suitable. Whereas male mealybug flight towards a pheromone source is restricted to a few hours, the male may continue mating activity throughout its sexually active period.

Mealybugs (Hemiptera: Pseudococcidae) are common invasive pests in Europe, causing major problems on crops and ornamental plants. However, very few data are available concerning the mealybug fauna of southern Europe. This lack of data and the difficulty of identifying mealybugs morphologically by traditional techniques currently limit the perspectives for efficient specific pest management. The aim of this study was to provide multi-criterion characterization of mealybugs surveyed in eastern Spain in order to facilitate their routine identification through DNA sequencing or the use of derived species-specific molecular tools. We characterised 33 mealybug populations infesting crops and ornamental plants in eastern Spain, using a combination of molecular and morphological techniques, including the sequencing of the universal barcode DNA region cytochrome c oxidase subunit I (COI). This characterisation has led to the identification of ten species and provides sequence data for three previously unsequenced species, contributing to the phylogenetic knowledge of the family Pseudococcidae. In addition, the intraspecific variations found in the populations of five mealybug species provide insight into their invasion history.

Although DNA barcode coverage has grown rapidly for many insect orders, there are some groups, such as scale insects, where sequence recovery has been difficult. However, using a recently developed primer set, we recovered barcode records from 373 specimens, providing coverage for 75 species from 31 genera in two families. Overall success was >90% for mealybugs and >80% for armored scale species. The G·C content was very low in most species, averaging just 16.3%. Sequence divergences (K2P) between congeneric species averaged 10.7%, while intra-specific divergences averaged 0.97%. However, the latter value was inflated by high intra-specific divergence in nine taxa, cases that may indicate species overlooked by current taxonomic treatments. Our study establishes the feasibility of developing a comprehensive barcode library for scale insects and indicates that its construction will both create an effective system for identifying scale insects and reveal taxonomic situations worthy of deeper analysis.

A survey was conducted in 47 locations in nine cotton-growing states of India to identify the composition of mealybug species occurring on cotton. Results of the taxonomic study showed that two mealybug species, the solenopsis mealybug, Phenacoccus solenopsis (Tinsley), and the pink hibiscus mealybug, Maconellicoccus hirsutus (Green), were found to infest cotton plants from all nine cotton growing states of the country. However, P. solenopsis was found to be the predominant mealybug species, comprising 95% of the samples examined. P. solenopsis, which was hitherto not reported to occur in India, now appears to be widespread on cotton in almost all cotton-growing states of the country. P. solenopsis is an exotic species originated from the USA and was reported to damage cotton and crops of 14 families. This report discusses the implications of the introduction of this exotic polyphagous pest species and the necessary steps to mitigate its potential threat to agriculture in India.

Molecular species identification is becoming more wide-spread in diagnostics and ecological studies, particularly with regard to insects for which morphological identification is difficult or time-consuming. In this study, we describe the development and application of a single-step multiplex PCR for the identification of three mealybug species (Hemiptera: Pseudococcidae) associated with grapevine in South Africa: Planococcus ficus (vine mealybug), Planococcus citri (citrus mealybug) and Pseudococcus longispinus (longtailed mealybug). Mealybugs are pests on many commercial crops, including grapevine, in which they transmit viral diseases. Morphological identification of mealybug species is usually time-consuming, requires a high level of taxonomic expertise and usually only adult females can be identified. The single-step multiplex PCR developed here, based on the mitochondrial cytochrome c oxidase subunit 1 (CO I) gene, is rapid, reliable, sensitive, accurate and simple. The entire identification protocol (including DNA extraction, PCR and electrophoresis) can be completed in approximately four hours. Successful DNA extraction from laboratory and unparasitized field-collected individuals stored in absolute ethanol was 97%. Specimens from which DNA could be extracted were always correctly identified (100% accuracy). The technique developed is simple enough to be implemented in any molecular laboratory. The principles described here can be extended to any organism for which rapid, reliable identification is needed.

From August 1988 to January 1997, natural enemies were reared from 335 colonies of Plnnococcus citri Risso (Homoptera: Pseudococcidae) sampled for 87 months from 225 randomly selected cocoa farms in the six cocoa-growing regions in Ghana. A total of 20,408 P. citri individuals was recorded, comprising adult females, third instar nymphs and mummified individuals harbouring parasitoids. Observed predators were larvae of Coccodiplosis coffeae Barnes (Diptera: Cecidomyiidae), nymphs and adults of Hyperaspis egregia Mader and Scymnus (Pullus) sp. (Coleoptera: Coccinellidae), as well as an unidentified lepidopteran. Twelve parasitic Hymenoptera were also reared, including Aenasius abengouroui (Risbec), Leptomastix dactylopii Howard, Anagyrus beneficions Compere, Tropidophryne melvillei Compere, Anagyrus amoenus Compere and Chryptochetum (Lestophonus) spp. Also recorded were a hyperparasitoid, Cheiloneurus carinatus Compere, parasitising Coc. coffeae, Xyplugaster pseudococci Risbec and six rare, undetermined parasitoids. Coccodiplosis coffeae was the commonest parasitoid, occurring throughout the year and infesting 72.8% of the P. citri colonies. Parasitism levels were generally low, the highest mean being 4.6 ± 2.6% for Aen. abengouroui. Simultaneous parasitism by more than one species was common and this gave rise to mean monthly parasitism levels ranging from 0.8 to 4.5%. Aenasius abengouroui, Ana. amoenus and H. egregia are being reported for the first time in P. citri on cocoa in Ghana, and the recovery of L. dactylopii suggests its establishment in the country, where it was introduced in 1949.

The effects of six constant temperatures ranging from 15 to 40°C on the rate of development, progeny production, sex ratio and adult longevity of the grape mealybug parasitoid, Anagyrus dactylopii (How.) were determined. It was found to complete the development in the temperature regimes of20–35°C but neither sex emerged as adults at 15 and 40°C. Developmental time of male and female decreased from 32.75 to 10 days, and from 34.50 to 11.75 days respectively, as the temperature increased from 20–35°C. Progeny production increased with the rise in temperature up to 30°C, and a maximum of 182 offspring emerged at 30°C. Sex ratio was altered considerably by different temperatures. Maximum female progeny was also obtained at 30°. Adult longevity of both sexes declined with increasing temperature. Mean longevity of male reduced from 2730 days at 15°C to 2.75 days at 40°C. The findings on the effects of temperature in relation to the rearing in the laboratory and the activity of Anagyrus dactylopii in the field are also discussed.

The striped mealybug, Ferrista virgata (Ckll.) has become a very serious pest of guava in India. Since the insecticides are ineffective, an attempt was made to suppress F. virgata with an introduced coccinellid, Cryptolaemus montrouzieri Mulsant C. montrouzieri and other local natural enemies especially Aenasius advena Comp. and Scymnus coccivora Ayyar effectively controlled F. virgata in guava orchards.

The pink mealybug Maconellicoccus (=Phenacoccus) hirsutus (Green) (Pseudococcidae: Hemiptera) occurs in more than 13 countries, but has a major pest status only in Egypt and India. Its biology, host range, ant association, natural enemies and methods of control are reviewed here.

The effect of exposing 1, 3 and 5 days old pupae to 10°C for periods of 7, 14, 21 and 28 days on the emergence, pre-oviposition and fecundity of Cryptolaemus montrouzieri Mulsant was studied. The emergence was delayed significantly when 1 and 3 days old pupae were subjected to 10°C for 28 days when compared to 5 days old pupae. The initiation of oviposition was delayed with the prolongation of holding time. The fecundity of females emerging from 5 days old pupae subjected to 10°C for 21 days was found to be significantly higher than in any other treatment.