Scientific name:
Hydrellia philippina Ferino
Common name: Rice whorl maggot

Translucent larva of rice whorl maggot, Hydrellia philippina Ferino

Feeding damage of rice whorl maggot with yellow spots, streaks, and deformations

Stunted plants caused by feeding of whorl maggot

Whorl maggot adult

Single, banana-shaped, white eggs of whorl maggot

Pupa of whorl maggot

Elongated egg of whorl maggot
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Taxonomy:
| Class |
Insecta |
| Order |
Diptera |
| Family |
Ephydridae |
Economic importance
Reports about the economic importance of the
whorl maggot are conflicting. Some suggest that infestation could lead to losses
of 30%, whereas others claim that even when crops are severely damaged there is
no reduction in yield. Recent investigations showed that the yield loss recorded
artifacts or loopholes. Whorl maggot damage can be compensated by plant growth.
Insecticide control is not recommended.
Geographical distribution
Bangladesh, Cambodia, India, Indonesia, Lao PDR,
Malaysia, Philippines, Thailand, Vietnam.
Morphology
Egg
The eggs are whitish and elongate. They are
banana-shaped with a hard shell as covering. A single egg measures 0.65-0.85 mm
long and 0.15-0.20 mm wide.
Larva
Larvae of the rice whorl maggot are legless.
Newly hatched larvae are transparent to light cream. Mature larvae are
yellowish. A mature larva is cylindrical with a pair of pointed spiracles found
posteriorly. It is 4.4-6.4 mm long and 0.5-0.7 mm wide.
Pupa
The pupa is dark brown and subcylindrical. Its
posterior end is tapering and has two terminal respiratory spines. The pupa is
4.8 mm long.
Adult
The gray adults have transparent wings. They
have a silvery white frons and cheeks. Their antennae are dark gray with a
silvery tinge in the inner portion of the second segment and 7-10 aristal hairs.
They have a grayish mesonotum with silvery white and brown tinges, whereas their
scutellum is silvery white to gray. Their abdomen is silvery white to gray with
blackish brown in the middle of the three basal segments. They have yellow legs
except for the femora.
The females are usually bigger than the males
and are 1.5-3.0 mm long.
Symptoms
Heavily damaged plants are stunted with few
tillers. The leaves have white or transparent patches. They easily break from
the wind. Slightly damaged leaves have pinholes.
Biology and ecology
H. philippina is a semi-aquatic whorl
maggot. It is common in irrigated fields and feeds on the central whorl leaf of
the vegetative stage of the rice plant. Direct-seeded fields and seedbeds are
not preferred by H. philippina. The adults are active during the day and
rest on rice leaves near the water. They prefer thick vegetation and are
attracted to open standing water around seedbeds.
The female adult lays 20 individual eggs. Eggs
are laid until 8 days. Individual eggs are laid on the leaf surface. They stick
to the leaves because of a gluey substance secreted by the female. Egg
incubation is 2-6 days. Neonate maggots feed on the unopened central leaves
where larval development is completed in 10-12 days. Before pupation, the mature
maggots leave the feeding site and pupate inside older tillers. Pupation is 5-10 days.
Host range
The rice whorl maggot’s primary host is rice.
It also feeds on grasses such as Brachiaria sp., Cynodon sp., Echinochloa
sp., Leersia sp., Leptochloa sp., Panicum sp., and wild
rice.
Detection and inspection
The damage symptoms of the whorl maggot are
visible as white or transparent patches and pinholes. At the maximum tillering
stage, these symptoms usually disappear.
Management
Cultural control
Since research has shown that the whorl maggot
does not cause economic losses, no control is needed.
Biological control
The eggs are parasitized by Opius sp., Tetrastichus
sp., and Trichogramma sp., and preyed upon by Dolichopus sp., Medetera
sp., and Syntormon sp. The adults are hosts to Lycosa
pseudoannulata (Boesenberg & Strand), Neoscona theisi (Walckenaer),
Ochthera brevitibialis de Meijere, and Oxyopes javanus (Thorell).
Chemical control
Insecticide control for whorl maggot damage is
not recommended. Damage symptoms often disappear in the crop’s maximum
tillering stage and are compensated by crops.
Selected references
Bandong JP, Litsinger JA. 1986. Oviposition of
rice whorl maggot (RWM) in wet seedbeds. Int. Rice Res. Newsl. 11(1):16-17.
Barrion AT, Litsinger JA. 1986. Ephydrid flies (Diptera: Ephydridae) of rice in the Philippines. Int. Rice Res.
Newsl. 11(4):29-30.
Barrion AT, Litsinger JA. 1994. Taxonomy of rice
insect pests and their arthropod parasites and predators. In: Biology and
management of rice insects. Manila (Philippines): International Rice Research
Institute. p 13-362.
Pathak MD, Khan ZR. 1994. Insect pests of rice.
Manila (Philippines): International Rice Research Institute. 89 p.
Reissig WH, Heinrichs EA, Litsinger JA, Moody K,
Fiedler L, Mew TW, Barrion AT. 1986. Illustrated guide to integrated pest
management in rice in tropical Asia. Manila (Philippines): International Rice
Research Institute. 411 p.
Shepard BM, Barrion AT, Litsinger JA. 1995.
Rice-feeding insects of tropical Asia. Manila (Philippines): International Rice
Research Institute. 228 p.
Shepard BM, Justo HD Jr., Rubia EG, Estaño DB.
1990. Response of the rice plant to damage by the rice whorl maggot Hydrellia
philippina Ferino (Diptera: Ephydridae). J. Plant Protect. Trop.
17(3):173-177.
Viajante VD, Heinrichs EA. 1986. Rice growth and
yield as affected by the whorl maggot Hydrellia philippina Ferino (Diptera:
Ephydridae). Crop Protect. 5(3):176-181.
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