common name: melonworm
scientific name: Diaphania hyalinata Linnaeus (Insecta: Lepidoptera: Pyralidae)
Distribution - Life Cycle and Description - Host Plants - Damage - Natural Enemies - Management - Selected References
Melonworm, Diaphania hyalinata Linnaeus, occurs throughout most of Central and South
America and the Caribbean. The United States is the northern limit of its permanent range, and
wintertime occurrence generally is limited to south Florida and perhaps south Texas.
Melonworm disperses northward annually. Its distribution during the summer months is
principally the southeastern states, though occasionally it disperses north to New England and
the Great Lakes region.
The melonworm can complete its life cycle in about 30 days. It is present throughout the year in
southern Florida, where it is limited mostly by availability of host plants. It disperses northward
annually, usually arriving in northern Florida in June and other southeastern states in July, where
no more than three generations normally occur before cold weather kills the host plants.
Egg: Melonworm moths deposit oval, flattened eggs in small clusters, averaging two to six eggs
per egg mass. Apparently they are deposited at night on buds, stems, and the underside of
leaves. Initially they are white or greenish, but soon become yellow in color. They measure
about 0.7 mm in length and 0.6 mm in width. Hatching occurs after three to four days.
eggs
closeup of eggs
Larva: There are five instars. Total larval development time is about 14 days, with mean (range)
duration the instars about 2.2 (2-3), 2.2 (2-3), 2.0 (1-3), 2.0 (1-3), and 5.0 (3-8) days,
respectively. Head capsule widths are about 0.22, 0.37, 0.62, 1.04, and 1.64 mm, respectively
(Smith et al. 1994). Larvae attain lengths of about 1.5, 2.6, 4.5, 10, and 16 mm in instars one
through five, respectively. Newly hatch larvae are colorless, but by the second instar larvae
assume a pale yellow-green color. They construct a loose silken structure under leaves which
serves to shelter them during the daylight hours. In the fifth instar, larvae have two subdorsal
white stripes extending the length of the body. The stripes fade or disappear just prior to
pupation, but they are the most distinctive characteristic of the larvae.
larva
Pupa: Prior to pupation, larvae spin a loose cocoon on the host plant, often folding a section of
the leaf for added shelter. The pupa is 12 to 15 mm in length, about 3 to 4 mm in width, and
fairly pointed at each end. It is light to dark brown in color. The pupal stage persists for nine to
10 days.
Adult: The moth's wingspan is about 2.5 cm. The wings are pearly white centrally, and slightly
iridescent, but are edged with a broad band of dark brown. Moths frequently display brushy
hairpencils at the tip of the abdomen when at rest. Melonworm moths remain in the crop during
the daylight hours. While they are generally inactive during the day, they will fly short distances
when disturbed. Smith (1911) provides a detailed account of melonworm biology.
adult
Melonworm is restricted to feeding on cucurbits. Both wild and cultivated cucurbits may be
attacked. Summer squash and the winter squash species are good hosts. Pumpkin is of variable
quality as a host, probably because pumpkins have been bred from several Cucurbita species.
The Cucumis species, cucumber, gerkin, and cantaloupe, are attacked but not preferred.
Watermelon is a rare host.
Melonworm feeds principally on foliage, especially if foliage of a favored host plant such as
summer or winter squash is available. Usually the leaf veins are left intact, resulting in lace-like
plant remains. However, if the available foliage is exhausted, or the plant is a less preferred
species such as cantaloupe, then the larva may feed on the surface of the fruit, or even burrow
into the fruit. Growers sometimes refer to these insects as "rindworms" because they cause scars
on the surface of melons. In a study of melonworm damage potential to summer squash
conducted in south Florida, melonworm caused a 23 % yield loss due to foliage damage (indirect
loss) and a 9 to 10% yield reduction due to fruit damage (direct loss) (McSorley and Waddill
1982). Kelsheimer (1949) considered this insect to be the most important pest of cucurbits in
Florida.
damage
Among the common natural enemies of melonworm are Apanteles sp., Hypomicrogaster
diaphaniae (Muesebeck), Pristomerus spinator (Fabricius) (all Hymenoptera: Braconidae),
Casinaria infesta (Cresson), Temelucha sp. (both Hymenoptera: Ichneumonidae), and
undetermined trichogrammatids (Hymenoptera: Trichogrammatidae) (Pena et al. 1987b,
Capinera 1994). However, additional species parasitized melonworm, including Gambrus
ultimus (Cresson), Agathis texana (Cresson) (both Hymenoptera: Ichneumonidae) and an
undetermined fly (Hymenoptera: Tachinidae). The tachinids known from melonworm are
Nemorilla pyste (Walker) and Stomatodexia cothurnata (Wiedemann). Studies conducted in
Puerto Rico (Medina-Gaud et al. 1989) reported levels of parasitism reaching 24%. Generalist
predators such as Calosoma spp. and Harpalus (both Coleoptera: Carabidae), the soldier beetle
Chauliognathus pennsylvanicus DeGeer (Coleoptera: Cantharidae), and the red imported fire ant
Solanopsis invicta Buren (Hymenoptera: Formicidae) have also been reported to be mortality
factors.
Sampling. Pheromone production by female moths peaks at about sunset (Valles and Capinera
1992). The sex pheromone has been identified (Raina et al. 1986) but is not available
commercially. Moths are not attracted to light traps. Therefore, checking plants for early stages
of leaf damage and the presence of arvae are the most effective ways to monitor crops.
Insecticides. Historically, melonworm was considered to be a very damaging pest, but because
it feeds preferentially on foliage it is easy to control with a variety of insecticides. In temperate
areas, and especially in commercial vegetable production areas, it is treated as only a minor pest.
In insecticide-free cucurbit production and in home gardens, melonworm can cause serious
damage.
Pollinators, particularly bees, are very important in cucurbit production, and insecticide
application can interfere with pollination by killing honeybees. If insecticides are to be applied
when blossoms are present, it is advisable to use insecticides with little residual activity, and to
apply insecticides late in the day, when bee activity is minimal.
Insect Management Guide for vegetables
Biological control. In addition to chemical insecticides, Bacillus thuringiensis is commonly recommended for suppression. The entomopathogenic nematode Steinernema carpocapsae
provides only moderate suppression because the nematodes do not survive long on the foliage,
where larvae are found resting and feeding (Shannag and Capinera 1995).
Cultural practices. Row covers can be used effectively to exclude melonworm adults (Webb
and Linda 1992). Intercropping of corn and beans with squash was shown to reduce damage by
melonworm (Letourneau 1986). Since melonworm prefers squash to most other cucurbits, trap
cropping has been suggested, and of course destruction of crop residue which may contain
melonworm pupae is recommended (Smith 1911). Early plantings, except in tropical areas
where melonworm overwinters, often escape serious damage.
- Capinera JL. 1994. Pickleworm and melonworm. Pages 140-145 In D. Rosen, Bennett FD,
Capinera JL (eds.). Pest Management in the Subtropics: Biological Control -- A Florida
Perspective. Intercept, Andover, United Kingdom.
-
Capinera JL. 2001. Handbook of Vegetable Pests. Academic Press, San Diego. 729 pp.
- Kelsheimer EG. 1949. Control of insect pests of cucumber and squash. Florida Agricultural Experiment Station Bulletin 465. 15 pp.
- Letourneau DK. 1986. Associational resistance in squash monocultures and polycultures in
tropical Mexico. Environmental Entomology 15: 285-292.
- Medina-Gaud S, Abreu E, Gallardo F, Franqui RA. 1989. Natural enemies of the
melonworm, Diaphania hyalinata L. (Lepidoptera: Pyralidae) in Puerto Rico. Journal of Agriculture of the University of Puerto Rico 73: 313-320.
- McSorley R, Waddill VH. 1982. Partitioning yield loss on yellow squash into nematode
and insect components. Journal of Nematology 14: 110-118.
- Pena JE, Waddill VH, Elsey KD. 1987a. Population dynamics of the pickleworm and
the melonworm (Lepidoptera: Pyralidae) in Florida. Environmental Entomology 16: 1057-1061.
- Pena JE, Waddill VH, Elsey KD. 1987b. Survey of native parasites of the pickleworm,
Diaphania nitidalis Stoll, and melonworm, Diaphania hyalinata (L.) (Lepidoptera: Pyralidae), in
southern and central Florida. Environmental Entomology 16: 1062-1066.
- Raina AK, Klun JA, Schwarz M, Day A, Leonhardt BA, Douglass LW. 1986. Female sex pheromone of the melonworm, Diaphania hyalinata (Lepidoptera: Pyralidae), and analysis of male responses to pheromone in a flight tunnel. Journal of Chemical Ecology 12: 229-237.
- Shannag HK, Capinera JL. 1995. Evaluation of entomopathogenic nematode species for
the control of melonworm (Lepidoptera: Pyralidae). Environmental Entomology 24: 143-148.
- Smith HA, Capinera JL, Pena JE, Linbo-Terhaar B. 1994. Parasitism of pickleworm
and melonworm (Lepidoptera: Pyralidae) by Cardiochiles diaphaniae (Hymenoptera:
Braconidae). Environmental Entomology 23: 1283-1293.
- Smith RI. 1910. Insect enemies of cantaloupes, cucumbers and related plants. North Carolina
Agricultural Experiment Station Bulletin 205. 40 pp.
- Smith RI. 1911. Two important cantaloupe pests. North Carolina Agricultural Experiment Station Bulletin 214: 101-146.
- Valles SM, Capinera JL. 1992. Periodicity of attraction of adult melonworm, Diaphania
hyalinata. Florida Entomologist 75: 390-392.
- Webb SE, Linda SB. 1992. Evaluation of spunbounded polyethylene row covers as a method of excluding insects and viruses affecting fall-grown squash in Florida. Journal of Economic Entomology 85: 2344-2352.
- Wilkerson JL, Webb SE, Capinera JL. (2005). Vegetable Pests III: Lepidoptera. UF/IFAS CD-ROM. SW 182.
Author: John L. Capinera, University of Florida
Photographs: Rita Duncan and John L. Capinera, University of Florida
Project Coordinator: Thomas Fasulo, University of Florida
Publication Number: EENY-163
Publication Date: October 2000. Latest revision: November 2005.
Copyright: 2000-2005 University of Florida
Featured Creatures
Department of Entomology and Nematology
Division of Plant Industry
Electronic Data Information Source