Liriomyza huidobrensis (serpentine leafminer)
- Taxonomic Tree
- Distribution Table
- Risk of Introduction
- Habitat List
- Hosts/Species Affected
- Host Plants and Other Plants Affected
- Growth Stages
- List of Symptoms/Signs
- Biology and Ecology
- Natural enemies
- Notes on Natural Enemies
- Means of Movement and Dispersal
- Plant Trade
- Wood Packaging
- Impact Summary
- Detection and Inspection
- Similarities to Other Species/Conditions
- Prevention and Control
- Distribution Maps
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PicturesTop of page
IdentityTop of page
Preferred Scientific Name
- Liriomyza huidobrensis (Blanchard, 1926)
Preferred Common Name
- serpentine leafminer
Other Scientific Names
- Agromyza huidobrensis Blanchard, 1926
- Liriomyza cucumifoliae Blanchard, 1938
- Liriomyza decora Blanchard, 1954
- Liriomyza dianthi Frick, 1958
- Liriomyza langei Frick, 1951
International Common Names
- English: leafminer; miner, pea leaf; pea leafminer; South American leafminer
- Spanish: minador de la hoja; minador pequeño; mosca minadora
- LIRIHU (Liriomyza huidobrensis)
- LIRILA (Liriomyza langei)
Taxonomic TreeTop of page
- Domain: Eukaryota
- Kingdom: Metazoa
- Phylum: Arthropoda
- Subphylum: Uniramia
- Class: Insecta
- Order: Diptera
- Family: Agromyzidae
- Genus: Liriomyza
- Species: Liriomyza huidobrensis
DescriptionTop of page
Size 0.2-0.3 mm x 0.10-0.15 mm, off-white and slightly translucent.
A maggot up to 3.25 mm in length. First-instar larvae are colourless on hatching, turning pale yellow-orange. Later instars are yellow-orange. The ratio of the cephalopharyngeal skeletons between the first and second instars is 1.80 and between the second and third instars is 1.47 (Head et al., 2002). The posterior spiracle forms a crescent with six to nine mounted pores.
The puparium is oval, slightly flattened ventrally, 1.3-2.3 × 0.5-0.75 mm, with variable colour from light brown to almost black.
Small, greyish-black, compact-bodied, 1.3-2.3 mm in body length, 1.3-2.3 mm in wing length. Females are slightly larger than males. In general, any agromyzid of this size with a bright yellow central area of the scutellum and bright yellow areas of the head and pleura, belongs to the genus Liriomyza. The subfamily Phytomyzinae has vein Sc becoming a fold distally, but not coalescing with vein R1 before reaching C; the genus Liriomyza has orbital setulae which are not proclinate (they may be reclinate or absent); 2 pairs orbital setae; C extending to M, which end in wing apex; cross vein DM-Cu present; scutellum yellow.
L. huidobrensis may be distinguished from other Liriomyza species by the head and leg yellow parts being a darker orange-yellow, the third antennal segments very dark, sometimes almost black on top, and the mesoplura is largely black. The overall appearance is of a small dark fly.
DistributionTop of page
L. huidobrensis originates in Central and South America and was absent from other continents until the 1980s. It was first detected in Europe in 1987 in the Netherlands where it was found on glasshouse lettuces; it is presumed to have been imported directly from South America. It has since spread considerably in Europe and especially the Mediterranean region, but particularly significant is the spread in central and eastern Europe where climatic conditions would be expected to deter its presence.
The pest previously believed to be pea leaf miner in the USA is actually Liriomyza langei (NAPPO, 2009).
L. huidobrensis has been intercepted, but is not established in Australia.
There are also reports from Italy, Guam, Comoros, Seychelles, Morocco, Syria, Java (east and west) and Korea.
Records for the Canary Islands, Spain and French Guiana (IIE, 1995) have not been confirmed.
See also CABI/EPPO (1998, No. 94).
Distribution TableTop of page
The distribution in this summary table is based on all the information available. When several references are cited, they may give conflicting information on the status. Further details may be available for individual references in the Distribution Table Details section which can be selected by going to Generate Report.Last updated: 13 May 2022
|Continent/Country/Region||Distribution||Last Reported||Origin||First Reported||Invasive||Reference||Notes|
|Ethiopia||Absent, Unconfirmed presence record(s)|
|South Africa||Present, Localized|
|Tanzania||Absent, Unconfirmed presence record(s)|
|Zambia||Absent, Unconfirmed presence record(s)|
|Cambodia||Absent, Unconfirmed presence record(s)|
|Israel||Present, Widespread||Introduced||First reported: 199*|
|Laos||Absent, Unconfirmed presence record(s)|
|North Korea||Present, Few occurrences|
|Sri Lanka||Present, Localized|
|Belgium||Absent, Formerly present|
|Czechia||Present, Few occurrences||Introduced||1993|
|Estonia||Absent, Confirmed absent by survey|
|Finland||Present, Few occurrences||Introduced||1997|
|Germany||Present, Few occurrences|
|Hungary||Present, Few occurrences|
|-Canary Islands||Present, Localized|
|Sweden||Absent, Intercepted only|
|United Kingdom||Absent, Eradicated||1989|
|-Northern Ireland||Absent, Eradicated|
|Dominican Republic||Present, Localized|
|Mexico||Absent, Unconfirmed presence record(s)|
|United States||Absent, Invalid presence record(s)|
|-California||Absent, Invalid presence record(s)|
|-Florida||Absent, Invalid presence record(s)|
|-Hawaii||Absent, Invalid presence record(s)|
|-Utah||Absent, Invalid presence record(s)|
|-Virginia||Absent, Invalid presence record(s)|
|-New South Wales||Present, Localized|
|Guam||Present, Few occurrences|
|Suriname||Absent, Unconfirmed presence record(s)|
Risk of IntroductionTop of page
Habitat ListTop of page
Hosts/Species AffectedTop of page
Host Plants and Other Plants AffectedTop of page
Growth StagesTop of page
SymptomsTop of page
In potato, feeding punctures can often be seen all over the growing plant, giving the impression that a generalized outbreak of larval infestation is in process. But the development of the larval damage follows a rather fixed pattern, somewhat different from that of the adult fly population. First, the initial larval infestation and corresponding damage occur in the lower third of the plant, moving upwards to the top of the plant. At this time, practically the whole above ground part of the plant becomes necrotic and dies. Larval damage is consistently less severe during vegetative growth stages than when the plant is full grown. The occurrence of egg extrusion in the growing leaves might explain this phenomenon (Mujica and Cisneros, 1997).
List of Symptoms/SignsTop of page
|Leaves / internal feeding|
Biology and EcologyTop of page
Peak emergence of adults occurs before midday (McGregor, 1914). Males usually emerge before females. Mating takes place from 24 h after emergence and a single mating is sufficient to fertilize all eggs laid. Female flies puncture the leaves of the host plants causing wounds which serve as sites for feeding or oviposition (Mujica and Cisneros, 1997). Feeding punctures cause the destruction of a larger number of cells and are more clearly visible to the naked eye. Approximately 15% of punctures made by L. trifolii and L. sativae contain viable eggs (Parrella et al., 1981). Males are unable to puncture leaves, but have been observed feeding at punctures produced by females. Both males and females are able to survive on dilute honey (in the laboratory) and take nectar from flowers.
Eggs are inserted just below the leaf surface. The number of eggs laid varies according to temperature and host plant. Eggs hatch in 2-5 days according to the temperature. The duration of larval development is generally 4-7 days at mean temperatures above 24°C (Harris and Tate, 1933). Reductions in population levels of L. huidobrensis occurred in California, USA, when the daily maximum temperature rose to 40°C (Lange et al., 1957). There are three larval stages that feed within the leaves. The larvae predominantly feed on the plant in which the eggs are laid. Although the larvae of some species can exit one leaf and enter another, this has not been reported for L. huidobrensis. The larva leaves the plant to pupate (Parrella and Bethke, 1984). Pupae may be found in crop debris or in the soil.
Pupation takes place within the sclerotized skin of the third larva and gives rise to adult flies. Parthenogenic females have not been reported. Pupariation is adversely affected by high humidity and drought. Adult emergence occurs 7-14 days after pupariation, at temperatures between 20 and 30°C (Leibee, 1982). At low temperatures emergence is delayed. In southern USA, the life cycle is probably continuous throughout the year, although there is a noticeable first generation which reaches a peak in April (Spencer, 1973). In Israel, adults can be found from the autumn to late spring but not in summer (Weintraub and Horowitz, 1996). Adults are primarily active in early morning, shortly after sunrise, and again just before sunset (Weintraub and Horowitz, 1996). In California, USA, it completes its life cycle in 17-30 days during the summer and in 50-65 days during the winter (Lange et al., 1957). Adults generally live for 15-30 days, and females generally live longer than males. In northern Europe, L. huidobrensis is mainly a glasshouse pest, but a proportion of puparia can survive outdoors during an average Dutch winter (van der Linden, 1993).
In Peru, the life cycle is as follows: egg stage (3-4 days); first-instar larva (3-4 days); second-instar larva, 2-3 days; third instar 3-4 days; pupal stage (12- 18 days). Females had an average longevity of 3-28 days; male longevity was 2-6 days. The mean number of eggs laid per female in winter was 117 and in spring was 161 (Mujica and Cisneros, 1997).
Studies on L. huidobrensis developmental rates in lettuce at different constant temperatures (11 to 28±1°C) revealed a linear increase with temperature (Head et al., 2002). The theoretical lower threshold temperatures for development for each larval instar and pupae were 5.35, 6.30, 6.20 and 5.7°C, respectively. The calculated degree-days for each stage were 84.3, 30.1, 58.9 and 143.7, respectively.
Similar studies were performed on beans (15-30°C)(Lanzoni et al., 2002). They estimated the minimum developmental temperatures for egg, larva and pupa at 8.1, 7.7 and 7.3°C, respectively. The upper thresholds for egg, larva and pupa were calculated to be 31.1, 35.3, and 27.9°C, respectively. Their data are similar to Prando and da Cruz (1986) and Vercambre and De Crozals (1993).
L. huidobrensis is from a tropical to warm temperate region and has been found up to 3000 m and has been shown to be more cold-hardy than its near relative L. sativae (Wang et al., 2000), surviving a super cooling point of -19.55°C and a freezing point of -18.7°C compared to L. sativae with a super cooling point of -9.96°C and a freezing point of -9.06°C. This behaviour gives L. huidobrensis a far greater climatic range for survival. Indeed, Chen and Kang (2004) evaluated populations in China from 25°N to 42°N and found increasing cold tolerance with latitude. Supercooling capacity ranged down to -23.9°C. Even in severe cold, some leafminers were able to survive. Interestingly, Martin et al. (2005) found that no L. huidobrensis survived the winter in southern Ontario, Canada.
Natural enemiesTop of page
|Natural enemy||Type||Life stages||Specificity||References||Biological control in||Biological control on|
|Bracon intercessor||Civelek et al. (2002)|
|Chrysocharis phytomyzae||Parasite||Arthropods|Larvae||Argentina||Vicia faba|
|Diglyphus crassinervis||Civelek et al. (2002)|
|Halticoptera circulus||Parasite||Arthropods|Larvae||USA; Hawaii||onions; Phaseolus vulgaris|
|Opius meracus||Civelek et al. (2002)|
Notes on Natural EnemiesTop of page
Salvo and Valladares (1995) reviewed the parasite complex of L. huidobrensis on faba beans (Vicia faba) in Colombia (part of its native range) and found that larval/pupal parasitoids caused a higher level of parasitism than purely larval parasitoids and that Opius scabriventris was the dominant species (52% parasitism). They also surveyed parasitoids on leafminers in Argentina (1999). In more recent work (2002) by these authors, they looked at the effect of 12 different plants on the size of L. huidobrensis and associated parasitoids. This could lead to improvement of commercially produced parasitoids for the control of the leafminer.
In Costa Rica, Hidalgo and Carballo (1991) found that weeds acted as natural reservoirs for parasitoids and in the same area Carballo et al. (1990) found that Diglyphus sp. was of similar importance to Opius spp.
In Portugese glasshouses the mirid bug Dicyphus cerastii preyed on L. huidobrensis and was a potential control agent (Carvalho et al., 2000).
A review of natural enemies and biological control of L. huidobrensis is provided by Waterhouse and Norris (1987).
An extensive review of biological control and IPM of L. huidobrensis is provided by Murphy and LaSalle (1999).
Means of Movement and DispersalTop of page
There is no information on the natural dispersal of L. huidobrensis, and very little information on dispersal in other species. Jones and Parrella (1986) measured the dispersal of L. trifolii in a chrysanthemum greenhouse and found that females flew signigicantly farther than males. Ozawa et al. (1999) measured the height at which L. trifolii fly in a greenhouse and found that they were primarily close to the plants. L. huidobrensis is a larger and stronger fly than L. trifolii.
L. huidobrensis is not carried phoretically by any other organism. It can be wind-blown into crops from surrounding vegetation/fields.
Liriomyza spp. do not transmit any pathogens. However, they may enhance the occurrence of plant pathogens. Adult females puncture both the upper and lower leaf surfaces (up to 100 punctures daily) to feed and lay eggs, leaving wounds which can serve as portals for bacteria and fungus and reduce photosynthesis. Since Chandler (1991) showed that the occurrence of leaf punctures from L. trifolii significantly increased the incidence of Alternaria leaf blight lesions (Alternaria cucumerina) on muskmelon leaves (Cucumis melo), it is possible that other leaf pathogens may be enhanced.
Plant TradeTop of page
|Plant parts liable to carry the pest in trade/transport||Pest stages||Borne internally||Borne externally||Visibility of pest or symptoms|
|Fruits (inc. pods)||arthropods/eggs; arthropods/larvae||Yes||Pest or symptoms usually visible to the naked eye|
|Leaves||arthropods/eggs; arthropods/larvae||Yes||Pest or symptoms usually visible to the naked eye|
|Stems (above ground)/Shoots/Trunks/Branches||arthropods/eggs; arthropods/larvae||Yes||Pest or symptoms usually visible to the naked eye|
|Plant parts not known to carry the pest in trade/transport|
|Growing medium accompanying plants|
|True seeds (inc. grain)|
Wood PackagingTop of page
|Wood Packaging not known to carry the pest in trade/transport|
|Loose wood packing material|
|Processed or treated wood|
|Solid wood packing material with bark|
|Solid wood packing material without bark|
Impact SummaryTop of page
|Fisheries / aquaculture||None|
ImpactTop of page
Damage is caused by larvae mining into leaves and petioles. The photosynthetic ability of the plants is often greatly reduced as the chlorophyll-containing cells are destroyed (Parrella and Bethke, 1984). Severely infested leaves may fall, exposing plant stems to wind action, and flower buds and developing fruit to scald (Musgrave et al., 1975). The presence of unsightly larval mines and adult punctures in the leaf palisade of ornamental plants can further reduce crop value (Smith et al., 1962; Musgrave et al., 1975). In young plants and seedlings, mining may cause considerable delay in plant development, leading to plant loss.
Detection and InspectionTop of page
Similarities to Other Species/ConditionsTop of page
Menken and Ulenberg (1986) have described a method to distinguish between L. bryoniae, L. huidobrensis, L. sativae and L. trifolii, using starch gel electrophoresis and enzyme staining. This method can be used on individual insects. Improved versions have recently been published by Oudman et al. (1995) and Collins (1996).
Knodel-Montz and Poe (1982) describe a method to distinguish L. huidobrensis from L. trifolii and L. sativa by the morphology of the ovipositor.
Kox et al. (2005) used the amplification of a 790 bp fragment of mitochondrial cytochrome oxidase II (COII) DNA, followed by RFLP, to distinguished species of Liriomyza including L. huidobrensis. This analysis was possible in larval, pupal and adult life stages.
DNA barcoding (a 527 pb fragment of mitochondrial cytochrome oxidase I (COI)) has been applied to the identification of leafminer species in the Philippines (Scheffer et al., 2006). The authors concluded that these technique can lead to rapid identifications.
Prevention and ControlTop of page
Due to the variable regulations around (de)registration of pesticides, your national list of registered pesticides or relevant authority should be consulted to determine which products are legally allowed for use in your country when considering chemical control. Pesticides should always be used in a lawful manner, consistent with the product's label.
Dacnusa sibirica is used as a biocontrol agent in glasshouses in Germany, but requires three to four releases per week (Leuprecht, 1992). In Dutch glasshouses, successful control was achieved using releases of D. sibirica in combination with Opius pallipes, in conjunction with the naturally present Diglyphus isaea (van der Linden, 1991). In Austria it was found that these parasitoids could be used in combination with cyromazine (Stolz and van Lenteren, 1996).
Control using nematodes can also be successful; Williams and Macdonald (1995) used foliar applications of Steinernema feltiae and species of Heterorhabditis (strain UK 211). Williams and Walters (2000) demonstrated that all three larval instars are equally susceptible to S. feltiae. Additional work was carried out to test the effects of some insecticides on the efficacy of S. feltiae; trichlorfon and dimethoate did not affect S. feltiae, but abamectin and deltamethrin reduced the nematodes ability to locate prey (Head et al., 2000).
Some varieties of potato are resistant to Liriomyza attack (Valencia and Campos, 1980). Resistance in potatoes has be ascribed to the high density of glandular trichomes (Anon, 1993). Mou and Liu (2003) examined 46 lettuce genotypes for resistance to L. langei. Wild species had significantly fewer leafminer punctures as compared to cultivated lettuce. This suggests that genetic improvement of cultivated lettuce to produce resistant varieties is feasible.
Some insecticides, particularly abamectin (Weintraub and Horowitz, 1998; Weintraub 2001; Hidrayani et al, 2005), the growth regulator cyromazine (Veire, 1991; Staay, 1992; Leuprecht, 1993; Weintraub and Horowitz, 1998; Weintraub 2001) and spinosad (Weintraub and Mujica, 2006) provide effective control against larvae because these insecticides are translaminar, but leaf miner resistance can sometimes make control of adults difficult (Parrella et al., 1984; Macdonald, 1991).
Some botanical insecticides are also effective in controlling larvae: Banchio et al. (2003) demonstrated that extracts of the fruit from Melia azedarach are effective against larvae and are a feeding deterrent to adults, resulting in rduced oviposition rates. Neem has also been shown to be effective against larvae (Weintraub and Horowitz, 1997; Civelek et al., 2002).
Integrated Pest Management
Cisneros and Gregory (1994) and Mujioca and Cisneros (1997) describe IPM practices for potato, developed by the International Potato Center (CIP), Peru. Other measures, such as physical barriers, are also effective (Ester, 1993).
All stages are killed within a few weeks by cold storage at 0°C. Newly-laid eggs are the most resistant stage and it is recommended that cuttings of infested ornamental plants be maintained under normal glasshouse conditions for 3-4 days after lifting, to allow eggs to hatch. Subsequent storage of the plants at 0°C for 1-2 weeks should then kill off leaf miner larvae (Webb and Smith, 1970).
To avoid the introduction of L. huidobrensis (and other leaf miner species) into further European countries, EPPO (OEPP/EPPO, 1990) recommended that propagating material (except seeds) of Capsicum, carnations, celery, chrysanthemums, Cucumis, Gerbera, Gypsophila, lettuces, Senecio hybridus and tomatoes from countries where the pests occur must have been inspected at least every month during the previous 3 months and found pest-free. A phytosanitary certificate should be required for cut flowers and for vegetables with leaves.
ReferencesTop of page
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Bahlai C A, Goodfellow S A, Stanley-Horn D E, Hallett R H, 2006. Endoparasitoid assemblage of the pea leafminer, Liriomyza huidobrensis (Diptera: Agromyzidae), in Southern Ontario. Environmental Entomology. 35 (2), 351-357. DOI:10.1603/0046-225X-35.2.351
Banchio E, Valladares G, Zygadlo J, Bogino P C, Rinaudi L V, Giordano W, 2007. Changes in composition of essential oils and volatile emissions of Minthostachys mollis, induced by leaf punctures of Liriomyza huidobrensis. Biochemical Systematics and Ecology. 35 (2), 68-74. DOI:10.1016/j.bse.2006.08.007
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Mujica N, Cisneros F, 1997. Developing IPM components for leafminer fly in the Ca±ete Valley of Peru. In: Program Report 1995-96, Lima, Peru: International Potato Center (CIP). 177-184.
Mujica N, Kroschel J, 2013. Pest intensity-crop loss relationships for the leafminer fly Liriomyza huidobrensis (Blanchard) in different potato (Solanum tuberosum L.) varieties. Crop Protection. 6-16. DOI:10.1016/j.cropro.2012.12.019
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Pan LiTing, Xu YongQiang, Du SuJie, Wang Wei, Yefremova Z, Dawa, Liu WanXue, 2019. First record of Liriomyza huidobrensis (Diptera: Agromyzidae) and a survey of its parasitoids in Tibet, China. Acta Entomologica Sinica. 62 (9), 1072-1080. DOI:10.16380/j.kcxb.2019.09.008
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Shiao ShiuhFeng, 2004. Morphological diagnosis of six Liriomyza species (Diptera: Agromyzidae) of quarantine importance in Taiwan. Applied Entomology and Zoology. 39 (1), 27-39. DOI:10.1303/aez.2004.27
Shiao ShiuhFeng, Wu WenJer, 2000. Liriomyza huidobrensis (Blanchard), a newly invaded insect of economic importance to Taiwan (Diptera: Agromyzidae). Plant Protection Bulletin (Taipei). 42 (4), 249-254.
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