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CITRUS
LEAFMINER, Phyllocnistis citrella Stainton (Lepidoptera:
Gracillariidae) (Contacts) Citrus Leafminer is a small
cosmopolitan leafminer that arrived in the Southern California (Imperial County)
around 2000 and has gradually moved its way northward. In Southern and
coastal California, the populations of citrus leafminer have been most severe
on the autumn terminal growth. Mature citrus trees can tolerate
leaf damage without appreciable harm to the tree or its fruit. As the
leafminer expands its range, local parasitoid species are likely to keep it
under sufficient control in mature orchards. Therefore, it is best to
avoid treating with insecticides that would disrupt those natural enemies. Young trees in the nursery
setting or newly planted trees in orchards can experience reduced tree growth
if the infestation of citrus leafminer is heavy and prolonged. At the
moment, Admire applied through the irrigation is the best method of
suppressing citrus leafminer in young trees (ca. 4 years old).
Various researchers from the University of California at Riverside, Cal Poly
San Luis Obispo, and the California Department of Food and Agriculture
Biological Control Program are studying the biological and chemical control
of this pest. Links to
Management of Citrus Leafminer View the Current Distribution of Citrus Leafminer in
California Commercial
Sources of CLM Pheromone Traps and Lures Recognizing Citrus Leafminer on Sticky Cards UC IPM Insecticide Guidelines for Citrus Leafminer How to Collect and Preserve Citrus Leafminer Parasites HISTORY The small leafmining moth, Phyllocnistis
citrella Stainton, family Gracillariidae (subfamily Phyllocnistinae), or
the citrus leafminer (CLM), was found in late May 1993 in several citrus
nurseries in Homestead, Florida, other parts of Dade County, Broward County,
and Colier County. CLM is a new world, continental United States, and Florida
resident. It is potentially a serious pest of citrus and related Rutaceae,
and some related ornamental plants (Beattie 1989; Clausen 1993; Kalshoven
1981). CLM has previously been intercepted in the United States in 1914
(ports not noted) on citrus and Atalantia sp. horticulture stock
imports from the Philippines (Sasser 1915). CLM is considered a potentially
serious threat to Florida citrus and native Rutaceae. It has not previously
been reported mining fruit rinds, but several possible cases have been
observed in
Adults of the
citrus leafminer are minute moths (4 mm wingspread) with white and silvery scales
on the forewings, with several black and tan markings, plus a black spot on
each wingtip. The hind wings and body are white, with long fringe scales
extending from the hind wing margins. In resting pose with wings folded, the
moth is much smaller in appearance (about 2mm). The head is very
smooth-scaled and white and the haustellum has no basal scales. Citrus
leafminer is most easily detected by its meandering serpentine larval mine,
usually on the ventral side of the leaf. Larvae are minute (to 3 mm),
translucent greenish yellow, and located inside the leaf mine. The pupa
characteristically is in a pupal cell at the leaf margin. Adults generally
are too minute to be easily noticed, and are active diurnally and evenings. DISTRIBUTION
A widespread Asian species
(Clausen 1931, 1993; CAB 1970), described from Calcutta, India (Stainton
1856), CLM now is known from East Africa - Sudan to Yemen (Badway 1967),
through southern Asia - Saudi Arabia to India (Fletcher 1920) and Indonesia
(Kalshoven 1981), North to Hong Kong and China, Philippines (Sasscer 1915),
Taiwan (Chiu 1985; Lo and Chiu 1988) and southern Japan (Clausen 1927). It is
also found in New Guinea and nearby Pacific Islands (CAB 1970), and Australia
(Beattie 1989; Hill 1918; Wilson 1991). CLM also occurs in South Africa and
more recently in parts of West Africa (CAB pers. comm.). The Australian
introduction occurred before 1940, and has since 1969 been reported from
northern Queensland. For the period from May to November 1993, CLM has spread
to all Florida citrus counties south of Tampa and Orlando, with isolated
sites as far north as Alachua and Wakulla Counties. The potential exists for
CLM spreading to Louisiana and Texas. HOST PLANTS
CLM is common on
species of citrus and related Rutaceae within its range (Kalshoven 1981). CLM
is most commonly found on leaves of grapefruit (Citrus X paradisi
Macfad.) and pummelo (pomelo) (Citrus maxima (Burm.) Merr. (Badawy
1967). Recorded Rutaceae include Aegle marmelos (L.) Corr. Serr. in
India (Fletcher 1920), Atalania sp. in the Philippines (Sasscer 1915),
Murraya paniculata (L.) Jack. in India (Pruthi and Mani 1945), Poncirus
trifoliata (L.) Raf. in India (Clausen 1933), and various native Rutaceae
in Indonesia (Kalshoven 1981). Other reported hosts include Jasminum
sambac (L.) Aiton (Oleaceae) in India (Fletcher 1920), mistletoes on
citrus (Loranthus spp., Loranthaceae) in the Philippines (Reinking and
Groff 1921), Pongamia pinnata (Leguminosae) in India (Margabandhu
1933), and Alseodaphne semecarpifolia Nees (Lauraceae) in India (Latif
and Yunus 1951). Florida records include various Citrus sp., Kumquat (Fortunella
crassifolia Swingle), and calamondin (X Citrofortunella microcarpa
(Bunge) D.O. Winjnands). Several other hosts have been reported for CLM but
larvae do not complete their life cycle on these incompatible hosts: Murraya
koenigii L. Sprengel (Rutaceae) in India (Fletcher 1920), Jasminum
sp. and Jasminum cinnamomum Kobuski (Oleaceae) in India (Pruthi and Mani
1945), Dalbergia sissoo Roxb. ex DC (Leguminosae) in India (Latif and
Yunus 1951), Salix sp. (Salicaceae) in India (Pruthi and Mani 1945),
and Grewia asiatica L. (Tiliaceae) in India (Latif and Yunus 1951). BIOLOGY
The biology of Citrus Leafminer has been reported on by a number of
researchers, including Badawy (1967), Beattie (1989), Clausen (1927, 1931,
1933), Fletcher (1920), Kalshoven (1981), Latif and Yunus (1951). Eggs of CLM
are laid singly on the underside of host leaves. Egg eclosion occurs within
2-10 days, whereupon larvae immediately enter the leaf and begin feeding.
Larvae make serpentine mines on young leaves (sometimes also young shoots),
resulting in leaf curling and serious injury. Leaf mines are usually on the
ventral leaf surface, except in heavy infestations when both leaf surfaces
are used. Usually only one leaf mine is present per leaf, but heavy
infestations can have 2 or 3 mines per leaf; up to 9 mines on large leaves
have been found in Florida. As with similar leafminers, larvae are protected
within the leaf during their feeding cycle. Larvae have 4 instars and
development takes from 5-20 days. Pupation is within the mine in a special
pupal cell at the leaf margin, under a slight curl of the leaf. Pupal
development takes 6-22 days. Adults emerge about dawn and are active in the
morning; other activity is at dusk or night. Females lay eggs evenings and at
night (Badawy 1967; Beattie 1989). CLM may help spread citrus canker (Hill
1918; Ando et al. 1985) because of leaf damage from the mine. Generations per
year appear to be continuous: 6 in southern Japan (Clausen 1931), 9-13 in
north central India (Lal 1950); 10 in southern India (Pandey and Pandey
1964). Development time totals about 13-52 days (Pandey and Pandey 1964),
depending on weather and temperate conditions. Adults live for only a few
days. Florida generations are produced about every 3 weeks.
Symptoms of infestation include: 1) leaves with serpentine mines, usually
on ventral surfaces; 2) curling of leaves (may harbor mealybugs); 3)
epidermis appearing as a silvery film over leaf mines; 4) pupation chamber
near leaf margin, the edge of which is rolled over, and exposed portion of
chamber with a distinct orange color; and 5) succulent branches of green
shoots may also be attacked (Beattie 1989; Pandey and Pandey 1964). CONTROL
Local species of
parasitoids adapt readily to the mines created by this insect. Thus, in time the infestations decline to
noneconomic levels unless disturbances such as insecticidal spraying
occur. Parasitoids
reported for CLM include 39 species from Southeastern Asia, Japan, and
Australia, mostly Chalcidoidea (Heppner 1993; Kalshoven 1981; Lo and Chiu
1988). A pheromone to attract males of CLM has been developed in Japan by
Ando et al. (1985), called (7Z, 11Z)-7,11-hexadecadienal. Most work has been
done using chemical control, especially in India. Various spray regimes,
timing of growth flushes, and promotion of biological control are recommended
in Australia (Beattie 1989). In Florida, chemical control recommendations are
still being evaluated, but biological control and semiochemical trapping may
be the most likely methods to help reduce populations of CLM in the long run.
REFERENCES: [Additional
references may be found at: MELVYL
Library ] LITERATURE CITED
Ando, T., K.Y Taguchi, M Uchiyama, T Ujiye, and H. Kuroko, 1985.
(7Z-11Z)-7,11-hexadecadienal: sex attractant of the citrus leafminer moth, Phyllocnistis
citrella Stainton (Lepidoptera, Phyllocnistidae). Agric.Biol. Chem. Tokyo
49:3633-3653. Badawy, A. 1967. The morphology and
biology of Phyllocnistis citrella Strait, a citrus leaf-miner in the
Sudan. Bull. Soc. Ent. Egypte 51:95-103. Beattie, G.A.C. 1989. Citrus Leaf miner. NSW Agric. and Fisheries, Agfact,
H2.AE.4:1-4. Chiu, S.C. 1985. Biological control of
citrus pests in Taiwan. Taiwan Agric. Res. Inst., Spec. Rep. 19:1-8. Clausen, C.P. 1927. The citrus insects
of Japan. USDA, Washington, D.C. Tech. Bul. 15:1-15. _______. 1931. Two citrus leaf miners
of the Far East. USDA, Washington, D.C. Tech. Bull. 252:1-13. _______. 1933. The citrus insects of tropical
Asia. USDA, Washington, D.C. Cir. 266:1-35. Commonwealth Agriculture Bureaux (CAB),
Commonwealth Institute of Entomology. 1970. Phyllocnistis
citrella Stnt. IN: Distribution maps of pests. Ser. A, Map No 274. The Eastern Press Ltd., London. Fletcher, T.B. 1920. Life histories of
Indian insects. Microlepidoptera. Mem. Dept. Agric. India 6:1-217, 68 pl. Heppner, J.B. 1993. Citrus Leafminer, Phyllocnistis citrella, in
Florida (Lepidoptera: Gracillariidae: Phyllocnistinae). Trop. Lepid.
4:49-64. Hill, G.F. 1918. History of citrus
canker in the Northern Territory (with notes of its occurrence elsewhere). N. Terr. Austr. Bull. 18:1-8. Kalshoven, L.G.E. 1981. Pests of crops in Indonesia. Jakarta: Ichtiar Baru. [reprint] Margabandhu, V. 1933. Insect pests of oranges in
the northern Circars. Madras Agric. J. 21:60-68. Lal, K.B. 1950. Insect-pests of fruit trees grown in the plains> Agric.
Anim. Husb. Uttar Pradesh 1:30-45. Latif, A., and C.M. Yunus. 1951. Food plants
of citrus leaf miner in Punjab. Bull. Ent. Res. 42:311-316. Lo, K.C., and S.C. Chiu. 1988. The
illustrations of citrus insect pests and their natural enemies in Taiwan.
Taichung: Taiwan Agric. Res. Inst. 75 p. Pandey. N.D., Y.D. Pandey. 1964. Bionomics
of Phyllocnistis citrella Stt. (Lepidoptera:
Gracillariidae). Indian J. Ent. 26:417-423. Pruthi, H.S., and M.S. Mani. 1945. Our
knowledge of the insect and mine pests of the citrus in India and their
control. Imp. Council Agric. Res. Sci. Monog. 16:1-42. Reinking, O.A., and G.W. Groff. 1921.
The kao pan seedless Siamese pummelo and its culture. Philipp. J. Sci.
19:389-437. Sasscer, E.R. 1915. Important insect pests collected on imported nursery stock
in 1914. J. Econ. Ent. 8:268-270. Stainton, H.T. 1856. Descriptions of
three species of Indian Micro-Lepidoptera. Trans. Ent. Soc. London (n.s.)
3:301-304. Wilson, C.G. 1991. Notes on Phyllocnistis
citrella Stainton (Lepidoptera: Phyllocnistidae) attacking four citrus
varieties in Darwin. J. Austr. Ent. Soc. 30:77-78. |