Crop Protection Compendium
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Crop Protection Compendium Datasheet report for Aleurodicus destructor (coconut whitefly) Top of page Pictures Picture Title Caption Copyright Top of page Identity Preferred Scientific Name Aleurodicus destructor Mackie, 1912 Preferred Common Name coconut whitefly Other Scientific Names Aleurodes albofloccosa Froggatt, 1918 Aleyrodicus destructor Mackie, 1912 International Common Names Spanish: mosca blanca del cocotero French: aleurode du cocotier EPPO code ALEDDE (Aleurodicus destructor) Top of page Taxonomic Tree Domain: Eukaryota Kingdom: Metazoa Phylum: Arthropoda Subphylum: Uniramia Class: Insecta Order: Hemiptera Suborder: Sternorrhyncha Unknown: Aleyrodoidea Family: Aleyrodidae Genus: Aleurodicus Species: Aleurodicus destructor / Top of page Notes on Taxonomy and Nomenclature A. destructor is regarded as a typical representative of the genus Aleurodicus, which is the type genus of the subfamily Aleurodicinae. The subfamily is defined by characters occurring in the adults (relatively rich forewing venation, based on a bifurcated vein R, plus the veins M and Cu; legs with paronychium in shape of a large spine; ventral abdominal wax-producing areas usually arranged in three and four pairs, respectively in males and females) and the pupal cases (large wax-producing compound pores occurring on the subdorsum; lingula large, tongue-shaped, extending beyond the posterior margin of a vasiform orifice). It is considered that the few species of the genus Aleurodicus (including A. destructor) described from southern Asia and the western Pacific are probably not congeneric with the Neotropical representatives of the same genus (Martin, 1996). Top of page Description Egg Eggs are about 0.31 mm long, elongate in shape, and yellow to brownish, dusted with powdered wax. The stalk is short, bearing the egg in a prostrate position on the leaf. Fourth-instar nymph (pupal case) The pupal case is yellowish to brownish, subelliptical to ovate in shape, sometimes with a narrowed cephalad, 1.3-1.5 mm long and 0.8-1.0 mm wide, covered by a copious secretion of white wax. On infested leaves, specimens of A. destructor may be completely hidden by wax. The wax rods, emerging from compound pores, are unusually long, attaining in more perfect specimens a length of 12-15 mm; they are generally broken and intermingled with bands or plates of wax from the marginal tubes. The subdorsum has wax-producing compound pores; one cephalic (smaller than the other ones) and six abdominal pairs, the latter ones are similar in size (up to 90 µm in diameter). Only scattered tiny pores, without a submarginal zone of wide-rimmed pores punctuate the remainder of the dorsal surface. A vasiform orifice is subcordate, about as wide as it is long. The operculum is subrectangular, about twice as wide as it is long. The lingula is large, tongue-shaped, and extends beyond the posterior margin of the vasiform orifice and bears four setae, of which two are much reduced. This is the stage used for identification purposes. Adults The vertex is rounded. The antennae have seven segments, of which the third is the longest. Forewings have veins R1, Rs and M present, sometimes with an indication of the Cu. Legs have the paronychium represented by a large spine. Male claspers are long and narrow; the penis is recurved and short. Top of page Distribution The subfamily Aleurodicinae is mostly Neotropical in distribution. However, A. destructor remains largely restricted to its native Austro-Oriental-Pacific zoogeographical region. / Top of page Distribution Table The distribution in this summary table is based on all the information available. When several references are cited, they may give conflicting information on the status. Further details may be available for individual references in the Distribution Table Details section which can be selected by going to Generate Report. Continent/Country/Region Distribution Last Origin First Invasive Reference Notes Reported Reported Asia Brunei Darussalam Present Mound and Halsey, (/cpc/datasheet/108378) 1978; Martin, 1985; EPPO, 2014 Cambodia Absent, EPPO, 2014 (/cpc/datasheet/108472) invalid record Indonesia Present EPPO, 2014 (/cpc/datasheet/108455) -Irian Jaya Present EPPO, 2014 (/cpc/datasheet/108713) -Java (/cpc/datasheet/108714) Present EPPO, 2014 -Sulawesi Present Mound and Halsey, (/cpc/datasheet/108718) 1978; Martin, 1985; Martin, 1988; EPPO, 2014 Laos (/cpc/datasheet/108481) Absent, EPPO, 2014 invalid record Malaysia Widespread EPPO, 2014 (/cpc/datasheet/108514) -Peninsular Malaysia Present EPPO, 2014 (/cpc/datasheet/108765) -Sarawak Present Mound and Halsey, (/cpc/datasheet/108767) 1978; Martin, 1985; EPPO, 2014 Philippines Present Mound and Halsey, (/cpc/datasheet/108535) 1978; Martin, 1985; EPPO, 2014 Singapore Widespread APPPC, 1987; (/cpc/datasheet/108557) Waterhouse, 1993; AVA, 2001 Thailand Present APPPC, 1987; (/cpc/datasheet/108580) Waterhouse, 1993 Vietnam Present Waterhouse, 1993; (/cpc/datasheet/108604) EPPO, 2014 Central America and Caribbean Saint Vincent and the Present EPPO, 2014 Grenadines (/cpc/datasheet/108600) South America Brazil (/cpc/datasheet/108381) Present EPPO, 2014 / Continent/Country/Region Distribution Last Origin First Invasive Reference Notes Reported Reported Oceania Australia Restricted EPPO, 2014 (/cpc/datasheet/108362) distribution -Australian Northern Territory Present NHM, 1996 (/cpc/datasheet/108619) -New South Wales Present Mound and Halsey, (/cpc/datasheet/108620) 1978; Martin, 1985; EPPO, 2014 -Queensland Present Mound and Halsey, (/cpc/datasheet/108621) 1978; EPPO, 2014 -Victoria Present Mound and Halsey, (/cpc/datasheet/108624) 1978 -Western Australia Present NHM, 1907 (/cpc/datasheet/108625) New Caledonia Present EPPO, 2014 (/cpc/datasheet/108517) Papua New Guinea Present Mound and Halsey, (/cpc/datasheet/108534) 1978; Martin, 1985; EPPO, 2014 Solomon Islands Present Mound and Halsey, (/cpc/datasheet/108553) 1978; Martin, 1985; EPPO, 2014 Vanuatu Present EPPO, 2014 (/cpc/datasheet/108605) Top of page Risk of Introduction A. destructor is usually considered as a quarantine pest and its spread over the tropics should be limited. Quarantine authorities in Europe (for example, UK) have occasionally intercepted it, but it has not become established. Top of page Hosts/Species Affected The host range of A. destructor is less wide than that of A. cocois or A. dispersus. A. destructor is most likely to be encountered on palms. Top of page Host Plants and Other Plants Affected Plant name Family Context Acacia (wattles) (/cpc/datasheet/1994) Fabaceae Wild host Annona squamosa (sugar apple) (/cpc/datasheet/5820) Annonaceae Other Banksia (/cpc/datasheet/8403) Proteaceae Wild host Cinnamomum (/cpc/datasheet/13508) Lauraceae Other Cocos nucifera (coconut) (/cpc/datasheet/11788) Arecaceae Main Ficus microcarpa (Indian laurel tree) (/cpc/datasheet/24130) Moraceae Wild host Phyllanthus acidus (star gooseberry) (/cpc/datasheet/46048) Euphorbiaceae Main Piper nigrum (black pepper) (/cpc/datasheet/41374) Piperaceae Other / Top of page Growth Stages Flowering stage, Fruiting stage, Post-harvest, Vegetative growing stage Top of page Symptoms A. destructor almost exclusively colonizes the leaves of host plants, on which the adults oviposit and the young larvae settle after having inserted their mouth stylets. On infested leaves, the occurrence of A. destructor is evidenced by the dense tangle of white wax filaments that are abundantly secreted by the nymphs (through dorsal compound pores). Moreover, spots of sticky and transparent honeydew appear in the leaf areas where individuals of A. destructor occur, and they soon become covered in black sooty mould. In case of heavy infestations, honeydew may come to cover the whole aerial part of the plant (leaves, stems and fruits) and this may lead to the plants acquiring an almost completely black appearance. Top of page List of Symptoms/Signs Sign Life Stages Type Fruit / honeydew or sooty mould Inflorescence / honeydew or sooty mould Leaves / honeydew or sooty mould Stems / honeydew or sooty mould Top of page Biology and Ecology A. destructor is usually a polyvoltine species, having continuous cycles throughout the year, at least where conditions are optimal and host plants are available. Top of page Notes on Natural Enemies The natural enemies of A. destructor are poorly known. Neuroptera (Chrysopa sp.), Coccinellidae (Scymnus sp.) and Syrphidae (Bacca sp.) are predators of A. destructor (Costa Lima, 1968). The chalcid wasp, Coccophagus sp. is a parasitoid of A. destructor (Sorauer, 1956). / Top of page Natural enemies Natural enemy Type Life Specificity References Biological Biological stages control in control on Baccha (/cpc/datasheet/8173) Predator Chrysopa Predator (/cpc/datasheet/16448) Coccophagus Parasite (/cpc/datasheet/14716) Scymnus (/cpc/datasheet/49353) Predator Top of page Impact A. destructor is an occasional pest in tropical Australia. Top of page Diagnosis A preparation of pupal cases in a slide mount (according to the procedures of Martin (1987)) may be used to confirm diagnosis. Martin and Watson (1998) provide a key to species of Aleurodicus on coconut in the Caribbean. Top of page Detection and Inspection The leaves, and especially their undersides, must be inspected for the characteristic waxy masses that indicate the occurrence of a nymphal colony. Sooty mould and honeydew coat surfaces below the colony. Top of page Similarities to Other Species/Conditions Several species of the genus Aleurodicus are crop pests. In addition to A. destructor,