common name: melon thrips
scientific name: Thrips palmi Karny (Thysanoptera: Thripidae)
In recent years melon thrips has spread from Southeast Asia to most of the rest of Asia, and to
many Pacific Ocean islands, North Africa, Australia, Central and South America, and the
Caribbean. In the United States it was first observed in Hawaii in 1982, Puerto Rico in 1986, and
Florida in 1990. It has the potential to infest greenhouse crops widely, but under field conditions
its distribution likely will be limited to tropical areas. In Florida, so far it is a field pest only
south of Orlando.
A complete generation may be completed in about 20 days at 30ºC, but it is
lengthened to 80 days when the insects are cultured at 15ºC. Melon thrips are able
to multiply during any season that crops are cultivated but are favored by warm weather. When
crops mature, their suitability for thrips declines, so thrips growth rate diminishes even in the
presence of warm weather. In southern Florida they are damaging on both autumn and spring
vegetable crops (Seal and Baranowski 1992, Frantz et al. 1995). In Hawaii, they also become
numerous on vegetables during the summer growing season (Johnson 1986).
thrips life cycle
Eggs: Eggs are deposited in leaf tissue, in a slit cut by the female. One end of the egg protrudes
slightly. The egg is colorless to pale white in color, and bean-shaped in form. Duration of the egg stage is about 16 days at 15ºC, 7.5 days at 26ºC, and 4.3 days at 32ºC.
Larvae: The larvae resemble the adults in general body form though they lack wings and are
smaller. There are two instars during the larval period. Larvae feed in groups, particularly along
the leaf midrib and veins, and usually on older leaves. Larval development time is determined
principally by the suitability of temperature, but host plant quality also has an influence. Larvae
require about 14, 5, and four days to complete their development at 15, 26, and 32ºC, respectively. At the completion of the larval instars the insect usually descends to the soil or leaf litter where it constructs a small earthen chamber for a pupation site.
larvae
Pupa: There are two instars during the "pupal" period. The prepupal instar is nearly inactive and
pupal instar is inactive. Both instars are nonfeeding stages. The prepupae and pupae resemble
the adults and larvae in form, except that they possess wing pads. The wing pads of the pupae
are longer than that of the prepupae. The combined prepupal and pupal development time is
about 12, 4, and 3 days at 15, 26, and 32ºC, respectively.
Adult: Adults are pale yellow or whitish in color, but with numerous dark setae on the body. A
black line, resulting from the juncture of the wings, runs along the back of the body. The
slender fringed wings are pale. The hairs or fringe on the anterior edge of the wing are
considerably shorter that those on the posterior edge. They measure 0.8 to 1.0 mm in body length,
with females averaging slightly larger than males. Unlike the larval stage, the adults tend to feed
on young growth, and so are found on new leaves. Adult longevity is 10 to 30 days for females and
seven to 20 days for males. Development time varies with temperature, with mean values of about 20,
17, and 12 days at 15, 26, and 32ºC. Females produce up to about 200 eggs, but averaging
about 50 per female. Both mated and virgin females deposit eggs.
adult
Careful examination is required to distinguish melon thrips from other common species. The
Frankliniella species are easily separated because their antennae consist of eight segments,
whereas in Thrips species there are seven antennal segments. To distinguish melon thrips from
onion thrips, Thrips tabaci Lindeman, it is helpful to examine the ocelli. There are three ocelli
on the top of the head, in a triangular formation. A pair of setae are located near this triangular
formation, but unlike the arrangement found in onion thrips, the setae do not originate within the
triangle. Also, the ocelli bear red pigment in melon thrips whereas they are grayish in onion
thrips. In general, the basic body color of adult melon thrips is yellow, but in onion thrips it is
yellowish gray to brown.
head and pronotum with setae identified
abdominal segments
metascutum and abdominal tergit II
The most complete summary of melon thrips biology and management is presented in Girling
(1992). Developmental biology is given by Tsai et al. (1995). Keys for identification of
common thrips are presented by Palmer et al. (1989) and Oetting et al. (1993).
Melon thrips is a polyphagous species, but is best known as a pest of Cucurbitaceae and
Solanaceae. Among vegetables injured are bean, cabbage, cantaloupe, chili, Chinese cabbage,
cowpea, cucumber, bean, eggplant, lettuce, melon, okra, onion, pea, pepper, potato, pumpkin,
squash, and watermelon. Tomato is reported to be a host in the Caribbean, but not in the United
States or Japan. Tsai et al. (1995) reported that cucurbits were more suitable than eggplant,
whereas pepper was less suitable than eggplant. Other crops infested include avocado, carnation,
chrysanthemum, citrus, cotton, hibiscus, mango, peach, plum, soybean, tobacco, and others.
thrips on bean
Melon thrips cause severe injury to infested plants. Leaves become yellow, white or brown, and
then crinkle and die. Heavily infested fields sometimes acquire a bronze color. Damaged
terminal growth may be discolored, stunted, and deformed. Densities from one to 10 per
cucumber leaf have been considered to be the threshold for economic damage in some Japanese
studies. However, studies in Hawaii suggested a damage threshold of 94 thrips per leaf early in
the growth of the plant (Welter et al. 1990). Feeding usually occurs on foliage, but on pepper, a
less suitable host, flowers are preferred to foliage. Because melon thrips prefer foliage, they are
reported to be less damaging to cucumber fruit than western flower thrips, Frankliniella
occidentalis (Pergande) (Rosenheim et al. 1990). Nevertheless, fruits may also be damaged;
scars, deformities, and abortion are reported. In Hawaii, thrips were observed to attain higher
densities on cucumber plants infected with watermelon mosaic virus, but it was not determined
whether the plants were more attractive to adults or suitable for survival and reproduction
(Culliney 1990).
bean leaf bronzing
bean leaf damage
eggplant leaf damage
eggplant damage
In addition to direct injury, melon thrips are capable of inflicting indirect injury by transmitting
some strains of tomato spotted wilt virus and bud necrosis virus.
Natural enemies, particularly predators, are important in the ecology of melon thrips. In fact,
there is strong indication that melon thrips abundance and damage are increased by application of
some insecticides (Etienne et al. 1990). Among the most important predators observed in Hawaii
were the predatory thrips Franklinothrips vespiformis (Crawford) (Thysanoptera:
Aeolothripidae) and especially the minute pirate bug Orius insidiosus (Say) (Hemiptera:
Anthocoridae). Other predators in Hawaii were the lady beetle Curinus coeruleus (Mulsant) (Coleoptera: Coccinellidae), Rhinacoa forticornis Reuter (Hemiptera: Miridae), and Paratriphleps laevisculus Champion (Hemiptera: Anthocoridae). Other predators and parasitoids are known in Asia (Hirose 1991, Hirose et al. 1993, Kajita 1986). The parasitoid. Ceranisus
menes Walker (Hymenoptera: Eulophidae) shows particular benefit in many Asian studies, and
this wasp has been introduced to Florida (Castineiras et al. 1996a). Fungi known to affect melon
thrips include Beauveria bassiana, Neozygites parvispora, Verticillium lecanii, and Hirsutella sp. (Castineiras et al. 1996b).
minute pirate bug
Sampling: Larvae and adults generally are found on foliage. Adults tend to move toward young
foliage, with nymphs tending to be clustered on foliage inhabited by adults several days earlier.
Adults can also be sampled with sticky and water pan traps. Blue and white are attractive colors
for thrips, and have been used to trap melon thrips. However, yellow has also been suggested to
be an attractive color (Culliney 1990).
Insecticides: Foliar insecticides are frequently applied for thrips suppression, but at times it has
been difficult to attain effective suppression. Various foliar and drench treatments, alone or
combined with oil, have achieved some success (Seal and Baranowski 1992, Seal et al. 1993,
Seal 1994) though it is usually inadvisable to apply insecticides if predators are present. The
eggs, which occur in the foliar tissue, and the pupae, which reside in the soil, are relatively
insensitive to insecticide application. For specific recommendations, see:
Insect Management Guide for vegetables
Cultural techniques: Several cultural practices apparently affect melon thrips abundance, but
few have been evaluated in the context of North American agriculture. Physical barriers such as
fine mesh and row cover material can be used to restrict entry by thrips into greenhouses, and to
reduce the rate of thrips settling on plants in the field.
Organic mulch is thought to interfere with the colonization of crops by winged thrips. Plastic
mulch also is reported to limit population growth, but it is uncertain whether this is due to
reduced rates of invasion or denial of suitable pupation sites. Crop stubble was not an effective
deterrent (Litsinger and Ruhendi 1984).
Heavy rainfall is thought to decrease thrips numbers (Etienne et al. 1990). However, there seems
to be no evidence that overhead irrigation is an important factor in survival.
Biological control: The predatory mite Neoseiulus cucumeris (Oudemans) has been investigated
for suppression of melon thrips (Castineiras et al. 1997). The mite density is correlated with
thrips density, but within-plant distribution differs among the two species, suggesting that
although the mites may increase in numerical abundance they are unlikely to drive the thrips to
extinction.
Host plant resistance: Nuessly and Nagata (1995) reported that susceptibility to injury varied
among pepper cultivars. They reported that although sweet and jalapeno types were sensitive to
foliar injury, cubanelle and cayenne types produced acceptable size and quality fruit. This is the
reverse of injury susceptibility to western flower thrips, so in areas with mixed thrips populations
growers cannot rely solely on plant selection to avoid damage.
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5: 109-166.
- Capinera JL. 2001. Handbook of Vegetable Pests. Academic Press, San Diego. 729 pp.
- Castineiras A, Baranowski RM, Glenn H. 1996a. Temperature response of tow strains of
Ceranisus menes (Hymenoptera: Eulophidae) reared on Thrips palmi (Thysanoptera: Thripidae).
Florida Entomologist 79: 13-19.
- Castineiras A, Baranowski RM, Glenn H. 1997. Distribution of Neoseiulus cucumeris
(Acarina: Phytoseiidae) and its prey, Thrips palmi (Thysanoptera: Thripidae) within eggplants in
south Florida. Florida Entomologist 80: 211-217.
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and Paecilomyces fumosoroseus (Deuteromycotina: Hyphomycetes) as biological control agents
of Thrips palmi (Thysanoptera: Thripidae). Florida
Entomologist 79: 458-461.
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cucumber infected with a mosaic virus. Proceedings of the Hawaiian Entomological Society 30: 85-89.
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precipitation on populations of Thrips palmi on aubergine (eggplant) in Guadeloupe. Florida Entomologist 73: 339-342.
- Frantz G, Parks F, Mellinger HC. 1995. Thrips population trends in peppers in
southwest Florida. Pages 111-114 In Parker BL, Skinner M, Lewis T (eds.). Thrips
Biology Management. Plenum Press, New York.
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International Institute of Biological Control, Silwood Park, Ascot, U.K. 37 pp.
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60 In N.S. Talekar (ed.). Thrips in Southeast Asia. Asian Vegetable Research and Development Center, Taipei, Taiwan.
- Hirose Y, Kajita H, Takagi M, Okajima S, Napompeth B, Buranapanichpan S. 1993.
Natural enemies of Thrips palmi and their effectiveness in the native habitat, Thailand. Biological Control 3: 1-5.
- Johnson MW. 1986. Population trends of a newly introduced species, Thrips palmi
(Thysanoptera: Thripidae), on commercial watermelon plantings in Hawaii. Journal of Economic Entomology
79: 718-720.
- Kajita H. 1986. Predation by Amblyseius spp. (Acarina: Phytoseiidae) and Orius sp.
(Hemiptera: Anthocoridae) on Thrips palmi Karny (Thysanoptera: Thripidae). Applied Entomology and Zoology 21: 484-484.
- Litsinger JA, Ruhendi. 1984. Rice stubble and straw mulch suppression of preflowering
insect pests of cowpeas sown after puddled rice. Environmental Entomology 13: 500-514.
- Nuessly GS, Nagata RT. 1995. Pepper varietal response to thrips feeding. Pages 115-118
In Parker BL, Skinner M, Lewis T (eds.), Thrips Biology and Management. Plenum
Press, New York.
- Oetting RD, Beshear RJ, Liu T-X, Braman SK, Baker JR. 1993. Biology and identification of thrips on greenhouse ornamentals. Georgia Agricultural Experiment Station Research Bulletin 414. 20 pp.
- Rosenheim JA, Welter SC, Johnson MW, Mau RFL, Gusukuma-Minuto LR. 1990. Direct feeding damage on cucumber by mixed-species infestations of Thrips palmi and Frankliniella occidentalis (Thysanoptera: Thripidae). Journal of Economic Entomology 83: 1519-1525.
- Welter SC, Rosenheim JA, Johnson MW, Mau RFL, Gusukuma-Minuto LR. 1990. Effects of Thrips palmi and western flower thrips (Thysanoptera: Thripidae) on the yield, growth, and carbon allocation pattern in cucumbers. Journal of Economic Entomology 83: 2092-2101.
- Seal DR. 1994. Field studies in controlling melon thrips, Thrips palmi Karny (Thysanoptera:
Thripidae) on vegetable crops using insecticides. Proceedings of the Florida State Horticultural Society 107: 159-162.
- Seal DR, Baranowski RM, Bishop JD. 1993. Effectiveness of insecticides in controlling Thrips palmi Karny (Thysanoptera: Thripidae) on different vegetable crops in south Florida. Proceedings of the Florida State Horticultural Society 106: 228-233.
- Tsai JH, Yue B, Webb SE, Funderburk JE, Hsu HT. 1995. Effects of host plant and
temperature on growth and reproduction of Thrips palmi (Thysanoptera: Thripidae). Environmental
Entomology 24: 1598-1603.
Author: J.L. Capinera, University of Florida
Photographs and Illustrations: John Capinera and James Castner, University of Florida; and Division of Plant Industry
Project Coordinator: Thomas R. Fasulo, University of Florida
Publication Number: EENY-135
Publication Date: June 2000. Latest revision: August 2004.
Copyright 2000-2004, University of Florida
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