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Pinnaspis strachani (Cooley)

Hibiscus Snow Scale
Hosts Distribution Damage Biology Behavior Management Reference


Victoria L. Tenbrick, Research Associate

Arnold H. Hara, Entomologist

Beaumont Research Center

Hilo, Hawaii

Updated by: J.M. Diez April 2007


Hosts include asparagus, avocado, bird of paradise, carambola, cherimoya, chinaberry, citrus, coconut palm, croton, cycads, dracaena, ferns, geranium, hala, hi'aloa, hibiscus, jacaranda, Iychee, mango. Mexican creeper, native cotton, oleander, pikake, plumeria, poinciana, red pepper, sweet potato, ti and wisteria. This is a short list out of over 150 plant hosts listed for hibiscus snow scale (Deckle 1965).


Widespread. An immigrant to the Hawaiian Islands, hibiscus snow scale was first recorded in 1910 (Zimmerman 1948).


The first sign of hibiscus snow scale is the presence of armor on upper and lower leaf surfaces, fruits, and stems of plants. The female armor is about 1.5 to 2 5 mm long (1/16 to 1/8th inch). The adult female armor is flat, irregularly oyster sheIl or pear-shaped, tough, white or dirty white. The cast skins of the nymph form a yellowish-brown spot, called a terminal exuvium, at the narrow end of the armor (Dekle 1965). Male armor is also white, but smaller (1 mm, which is less than l/16 inch). Males are long and narrow with three ridges running lengthwise. The armor must be pried off to reveal the insect. Females and feeding nymphs are attached to the plant by hair-like mouthparts. The female body is a flat, elongated oval shape without wings, legs, or eyes, Dead ones are dark brown and are dried rather than plump. Armored scales feed on plant juices and cause loss of vigor, deformation of infested plant parts, yellowish spots on leaves, loss of leaves, and even death of the plant (Dekle 1965, Beardsley & Gonzalez 1975). Since scales are spread by introduction of infested material and are difficult to identify to species outside of the lab, scales of the genus Pinnaspis are a quarantine problem on exported potted plants, cut flowers, and cut foliage.


The number of days for each developmental stage and the number of generations per year depend on temperature, humidity, and rainfall (Beardsley & Gonzalez 1975) Based on a generalized life history of other tropical species, 30 days is the approximate time to complete the life cycle from egg to reproducing adult.


Eggs are laid under the armor of the female where they develop and hatch.


The first stage after hatching is the only nymphal stage with legs, so the insects are called crawlers. Crawlers may stay under the maternal armor several hours until outside conditions, especially temperature and humidity, are good. After they leave the cover, they wander for a period ranging from minutes to days, but usually a few hours. At the end of the wandering period they flatten against the leaf or stem and begin to secrete their armor (Beardsley and Gonzalez, 1975).


Newly settled nymphs insert their piercing. sucking mouth parts into plant tissue and start feeding on plant juices. Female nymphs shed their skin twice as they grow and develop. Males have five stages, feeding and building armor only in the first two stages. The cast skins, called exuviae, are incorporated into the armor at the narrow end forming a dot. The armor is non-living and is made of cast skins, threads, and liquid, all produced by the insect (Beardsley and Gonzalez 1975).


Female hisbiscus snow scales appear larvae-like. They remain under armor in one place throughout their lives to feed and reproduce. Males are very different in appearance and behavior from females. They are tiny, winged creatures with eyes and legs. When mature they emerge from the armor in the late afternoon, living only a few hours to mate. Mate-finding is probably aided by pheromones secreted by females Beardsley & Gonzalez 1975). Because of the late emergence and short life of males, it is unlikely to find them in the field.


Since female armored scales are not capable of wandering once they have settled and started feeding, long range dispersal happens by passive transport of infested plant material. Short range dispersal happens as crawlers search out places to settle and feed (Beardsley & Gonzalez 1975). It is the crawler stage that can be carried directly from place to place by people, animals, birds, ants, and wind currents (Deckle 1965, Beardsley and Gonzalez 1975). Wind is an agent of dispersal and also one of mortality, since crawlers dislodged by wind may not land on suitable host plants. Adult males are capable of only weak flight or wind transport. Living only a few hours, they do not feed.


Cultural control

Since armored scales are spread chiefly through movement of nursery stock, only propagative material that is free of scales should be planted. Adequate plant spacing is important because armored scales seldom spread from plant to plant unless the crowns of the plants are in contact (Beardsley & Gonzalez, 1975). As plants grow,. pruning maintains spacing and allows maximum coverage when using insecticides.

Biological control -- Predators

Ladybird beetles, or ladybugs, have been introduced and become established in Hawaii to control armored scales. Some of these, such as Telsimia nitida Chapin, (Coleoptera: Coccinellidae) have become established on the major islands. These beetle adults and larvae are carnivorous, eating soft-bodied insects. Scale covers that look chewed and have no insect underneath are signs that predators have been feeding on the scales.

Biological control -- Parasites

Tiny wasps lay eggs in developing scales. They are parasites that absorb food from the scale body. Instead of an adult scale under the cover, an adult wasp emerges. These can be very effective in controlling armored scales (Dekle, 1965). In Hawaii The wasp Aspidiotiphagus citnnus Crawford (Hymenoptera: Aphelinidae) parasitizes hibiscus snow scale (Zimmerman 1948).

Mechanical Control

Scraping and scrubbing to remove scale from plants are effective mechanical control tactics. Removing scales is especially important on exported plan; materials, since intact armor is a sign of scale infestation.


Insecticide mode of action and formulation are important because the armor covers and protects all stages but the crawler and the adult male. Contact insecticides target the crawlers stage; systemics target adult females and nymphs, as well as male nymphs. Since scales have natural enemies, care must be taken to conserve these. Populations of other pests, such as white flies and other scales, may rise if their natural enemies are affected by chemical control. Spraying should be determined by presence of scales in the field rather than by the calendar. Scales are best detected by regularly inspecting all areas of the fields for scales. When detected, directing spray at hot spots rather than uninfested areas helps conserve natural enemies and also delay pesticide resistance.

In the packing house, insecticidal soaps can be used in the cleaning water to kill crawlers while scrubbing off adults. Dipping without scrubbing in a soap-pyrethroid solution for five minutes is only 70% effective against adults and nymphs (Hansen et al. 1992). Even though scales are killed, it takes several days for the body to dry, so removal of the armor is required to assure inspectors that the plant material is insect free.


Beardsley, J. W. Jr. and R. H. Gonzalez. 1975. The biology and ecology of armored scales. Annual Review of Entomology. 20: 47-73.

Dekle, G. W. 1965. Arthropods of Florida Vol. 3, Florida Armored Scale Insects. Division of Plant Industry, Florida Department of Agriculture, Gainesville. 265 pages.

Hansen, J. D., A. H. Hara and V. L. Tenbrink. 1992. Insecticidal dips for disinfesting commercial tropical cut flowers and foliage. Tropical Pest Management 38: 245-249

Zimmerrnan, E. C. 1948. Insects of Hawaii Vol. S Homptera: Sternorhyncha University of Hawaii Press, Honolulu. 464 pp.






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