Invasive Species Compendium

Detailed coverage of invasive species threatening livelihoods and the environment worldwide


Aonidiella orientalis
(oriental yellow scale)



Aonidiella orientalis (oriental yellow scale)


  • Last modified
  • 27 March 2018
  • Datasheet Type(s)
  • Invasive Species
  • Pest
  • Natural Enemy
  • Preferred Scientific Name
  • Aonidiella orientalis
  • Preferred Common Name
  • oriental yellow scale
  • Taxonomic Tree
  • Domain: Eukaryota
  •   Kingdom: Metazoa
  •     Phylum: Arthropoda
  •       Subphylum: Uniramia
  •         Class: Insecta
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Preferred Scientific Name

  • Aonidiella orientalis (Newstead, 1894)

Preferred Common Name

  • oriental yellow scale

Other Scientific Names

  • Aonidiella cocotiphagus (Marlatt) Ferns, 1938
  • Aonidiella taprobana (Green) MacGillivray, 1921
  • Aspidiotus cocotiphagus Marlatt, 1908
  • Aspidiotus orientalis Newstead, 1894
  • Aspidiotus osbeckiae Green, 1896
  • Aspidiotus pedronis Green, 1905
  • Aspidiotus taprobanus Green, 1905
  • Chrysomphalus orientalis (Newstead) Lindinger, 1913
  • Chrysomphalus pedroniformis Cockerell & Robinson, 1915
  • Chrysomphalus pedronis (Green) Sanders, 1906
  • Evaspidiotus orientalis (Newstead) Leonardi, 1898
  • Furcaspis orientalis (Newstead) MacGillivray, 1921

International Common Names

  • English: oriental red scale; oriental scale; scale, oriental; scale, oriental red; scale, oriental yellow; scale, red

EPPO code

  • AONDOR (Aonidiella orientalis)

Taxonomic Tree

Top of page
  • Domain: Eukaryota
  •     Kingdom: Metazoa
  •         Phylum: Arthropoda
  •             Subphylum: Uniramia
  •                 Class: Insecta
  •                     Order: Hemiptera
  •                         Suborder: Sternorrhyncha
  •                             Unknown: Coccoidea
  •                                 Family: Diaspididae
  •                                     Genus: Aonidiella
  •                                         Species: Aonidiella orientalis

Notes on Taxonomy and Nomenclature

Top of page Aonidiella orientalis was first described by Newstead in 1894, as Aspidiotus orientalis, from an undetermined host in India. It has been redescribed as Aspidiotus osbeckiae Green, from Osbeckia in Sri Lanka, as Aspidiotus cocotiphagus Marlatt, from coconut in Cuba, and as Chrysomphalus pedroniformis Cockerell and Robinson, from grapes in the Philippines. This armoured scale is now located in the genus Aonidiella Berlese and Leonardi, within the tribe Aspidiotini of the subfamily Diaspidinae (McKenzie, 1938).


Top of page As with all armoured scale species (Diaspididae), adults of A. orientalis are covered with a scale or cover that is morphologically separate from the body. The adult female is less strongly reniform than typical for its genus, with less developed prosomatic lobes (McKenzie, 1938).

The adult female scale cover is circular and flat in shape, almost white to pale brown or yellow, with yellow to dark brown exuviae positioned more or less centrally. Adult female insect with prosoma pyriform, expanding to subcircular and becoming moderately sclerotized around margins at maturity. Pygidium quite well sclerotized dorsally. Median lobes distinctly larger than second lobes, with fourth lobes represented by small points on either side. Plates lateral to third lobes not fringed, each with a long fleshy process present at mesal angle. Abdominal segments 1 to 3 with a submarginal row or cluster of dorsal macroducts present on each side. Thoracic tubercles are minute. Perivulvar pores present in 4 or 5 groups, ranging from 19 to 32 in number. Prevulvar scleroses and apophyses absent. Adult females measure 1.0-1.4 mm in length when slide-mounted (Williams and Watson, 1988).

Male scales are elongate to oval in shape and similar to females, but smaller, with yellow exuviae near one end (Williams and Watson, 1988).


Top of page A. orientalis is a tropical and subtropical species with a wide distribution, including the West Indies, Middle East, India, East Africa and South Africa, southern Asia and northern Australia (CIE, 1978). It has been accidentally distributed worldwide on host plants and also occurs in greenhouses in temperate areas.

Distribution Table

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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.

Continent/Country/RegionDistributionLast ReportedOriginFirst ReportedInvasiveReferenceNotes


BangladeshPresentNHM, 1927
ChinaPresentPresent based on regional distribution.
-GuangdongPresentCIE, 1978
-Hong KongPresentNHM, 1976
IndiaPresentCIE, 1978
-Andaman and Nicobar IslandsPresentCIE, 1978
-Andhra PradeshPresentCIE, 1978
-BiharPresentCIE, 1978
-DelhiPresentNHM, 1980
-GujaratPresentNHM, undated
-Himachal PradeshPresentVerma and Dinabandhoo, 2005
-Indian PunjabPresentNHM, 1978
-KarnatakaPresentShafee and Fatma, 1984
-KeralaPresentNHM, 1983
-Madhya PradeshPresentCIE, 1978
-MaharashtraPresentCIE, 1978
-OdishaPresentNHM, 1993
-Tamil NaduPresentCIE, 1978
-Uttar PradeshPresentCIE, 1978
-West BengalPresentNHM, 1956
IranPresentCIE, 1978
IraqPresentCIE, 1978
IsraelPresentWysoki, 1997
MalaysiaPresentPresent based on regional distribution.
-Peninsular MalaysiaPresentCIE, 1978
MaldivesPresentNHM, 1994
MyanmarPresentNHM, 1918
NepalPresentCIE, 1978
OmanPresentNHM, 1992; Elwan, 2000
PakistanPresentCIE, 1978
PhilippinesPresentCIE, 1978
Saudi ArabiaPresentCIE, 1978
Sri LankaPresentCIE, 1978
ThailandPresentNHM, 1994
United Arab EmiratesPresentNHM, undated


AngolaPresentNHM, 1972
CameroonPresentNHM, 1992
EgyptPresentNHM, 1988
EthiopiaPresentCIE, 1978
KenyaPresentCIE, 1978
MaliPresentMuniappan et al., 2012
NigerPresentNHM, 1994
NigeriaPresentNHM, 1994
Saint HelenaPresentNHM, 1959
SenegalPresentMuniappan et al., 2012
SomaliaPresentCIE, 1978
South AfricaPresentCIE, 1978
SudanPresentCIE, 1978
TanzaniaPresentCIE, 1978
ZambiaPresentNHM, 1996

North America

MexicoPresentCIE, 1978; Arriola et al., 2016
USAPresentPresent based on regional distribution.
-FloridaPresentCIE, 1978

Central America and Caribbean

Antigua and BarbudaPresentNHM, 1971
BahamasPresentCIE, 1978
BarbadosPresentCIE, 1978
CubaPresentCIE, 1978
CuraçaoPresentCIE, 1978
Dominican RepublicPresentCIE, 1978
GuadeloupePresentCIE, 1978
HaitiPresentCIE, 1978; Schotman, 1989
JamaicaPresentCIE, 1978
MartiniquePresentCIE, 1978
Netherlands AntillesPresentCIE, 1978
PanamaPresentCIE, 1978
Puerto RicoPresentCIE, 1978
Saint Kitts and NevisPresentNHM, 1996
Trinidad and TobagoPresentCIE, 1978
United States Virgin IslandsPresentNHM, 1979

South America

BrazilPresentMcKenzie, 1938
-CearaPresentCosta et al., 2013
EcuadorPresentNHM, 1984


AustraliaPresentPresent based on regional distribution.
-Australian Northern TerritoryPresentCIE, 1978
-QueenslandPresentCIE, 1978
NauruPresentNHM, undated
Papua New GuineaPresentWilliams and Watson, 1988

Risk of Introduction

Top of page Diaspididae are generally of quarantine importance, as they are primarily spread on plant stock through human activity. They are regularly intercepted at plant quarantine inspection centres.

A. orientalis was reported to be relatively new to the South Pacific area by Williams and Watson (1988), and therefore to be of potential phytosanitary risk. In the Caribbean it is regarded as an economic plant pest of quarantine importance (Schotman, 1989).

Hosts/Species Affected

Top of page A. orientalis is highly polyphagous. It can attack almost any host except conifers, according to Williams and Watson (1988). It can be an economic pest of crops from diverse families. These include: species of Citrus and Ficus, mango, papaya, bananas and other fruits; palm trees, including coconut and arecanut (Areca catechu); and tea (Camellia sinensis).

The distribution map includes records based on specimens of A. orientalis from the collection in the Natural History Museum (London, UK). These are noted in the List of Countries (NHM, undated).

Host Plants and Other Plants Affected

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Plant nameFamilyContext
Acacia (wattles)FabaceaeWild host
Aegle marmelos (golden apple)RutaceaeOther
AgaveAgavaceaeWild host
Agave sisalana (sisal hemp)AgavaceaeOther
Albizia lebbeck (Indian siris)FabaceaeWild host
AnnonaAnnonaceaeWild host
Annona squamosa (sugar apple)AnnonaceaeOther
Azadirachta indica (neem tree)MeliaceaeOther
Bauhinia variegata (mountain ebony)FabaceaeOther
Calotropis gigantea (Yercum fibre)ApocynaceaeOther
Calotropis procera (apple of sodom)ApocynaceaeOther
CamelliaTheaceaeWild host
Camellia sinensis (tea)TheaceaeMain
Carica papaya (pawpaw)CaricaceaeMain
Cassia fistula (Indian laburnum)FabaceaeOther
Cocos nucifera (coconut)ArecaceaeMain
Codiaeum variegatum (croton)EuphorbiaceaeWild host
Cucurbita (pumpkin)CucurbitaceaeOther
Cycas revoluta (sago cycas)CycadaceaeOther
Dalbergia sissooFabaceaeOther
Elaeis guineensis (African oil palm)ArecaceaeOther
EugeniaMyrtaceaeWild host
FeijoaMyrtaceaeWild host
Ficus benghalensis (banyan)MoraceaeOther
Ficus benjamina (weeping fig)MoraceaeOther
Ficus carica (common fig)MoraceaeOther
Gossypium hirsutum (Bourbon cotton)MalvaceaeOther
Hedera (Ivy)AraliaceaeWild host
Hibiscus (rosemallows)MalvaceaeWild host
Litchi chinensis (lichi)SapindaceaeOther
Mangifera indica (mango)AnacardiaceaeMain
Manilkara zapota (sapodilla)SapotaceaeMain
Melia azedarach (Chinaberry)MeliaceaeOther
Morus nigra (black mulberry)MoraceaeOther
Musa (banana)MusaceaeOther
Nerium oleander (oleander)ApocynaceaeOther
Olea europaea subsp. europaea (European olive)OleaceaeOther
Persea americana (avocado)LauraceaeOther
Phoenix dactylifera (date-palm)ArecaceaeOther
Pistacia lentiscus (mastic)AnacardiaceaeOther
Plumeria (frangipani)ApocynaceaeOther
Polyphagous (polyphagous)Main
Prunus (stone fruit)RosaceaeOther
Prunus persica (peach)RosaceaeOther
Psidium guajava (guava)MyrtaceaeMain
Punica granatum (pomegranate)PunicaceaeOther
Ravenala madagascariensisStrelitziaceaeOther
RicinusEuphorbiaceaeWild host
Ricinus communis (castor bean)EuphorbiaceaeOther
Rosa (roses)RosaceaeWild host
Salix (willows)SalicaceaeWild host
Schleichera oleosa (Macassar oil tree)SapindaceaeOther
Solanum (nightshade)SolanaceaeOther
Solanum arundoSolanaceaeOther
Spondias dulcis (otaheite apple)AnacardiaceaeOther
Syzygium cumini (black plum)MyrtaceaeOther
Tamarindus indica (Indian tamarind)FabaceaeMain
Vitis (grape)VitaceaeWild host
Vitis vinifera (grapevine)VitaceaeOther
ZiziphusRhamnaceaeWild host
Ziziphus jujuba (common jujube)RhamnaceaeOther
Ziziphus mauritiana (jujube)RhamnaceaeOther

Growth Stages

Top of page Flowering stage, Fruiting stage, Seedling stage, Vegetative growing stage


Top of page Direct feeding damage on leaves and removal of plant sap reduces plant vigour. Feeding often causes depressions, discoloration and distortion of leaves. Heavy infestations can result in the yellowing of foliage and defoliation, dieback of small twigs and premature fruit drop (Rajagopal and Krishnamoorthy, 1996). Cosmetic damage may also occasionally occur to fruits.

List of Symptoms/Signs

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SignLife StagesType
Fruit / discoloration
Fruit / external feeding
Leaves / abnormal colours
Leaves / abnormal forms
Leaves / abnormal leaf fall
Leaves / external feeding
Leaves / yellowed or dead
Stems / dieback
Stems / distortion
Stems / external feeding

Biology and Ecology

Top of page The eggs are laid under the female scale cover. The larvae (forst instar crawlers) emerge from under the female, and crawl for several hours until they find suitable host plant tissue into which to insert their stylets. The females subsequently remain immobile, with successive moults adding to the size of the scale. Females have two moults before attaining maturity. The males have additional prepupal and pupal moults before attaining a winged adult stage. Adult males lack mouthparts, do not feed and are relatively short-lived. Mating and the laying of eggs is the most important route by which crawlers are produced (Rajagopal and Krishnamoorthy, 1996).

In laboratory studies, males took an average of 19.5 days to proceed from the crawler stage to adult and females took an average of 44.2 days from the crawler stage to production of the first crawler of the subsequent generation (Elder and Smith, 1995).

In Iran, five generations per year were recorded, with the maximum population density in the fourth and fifth generations. Reproduction was most frequently viviparous, but oviparous and ovoviviparous reproduction were also observed (Khalaf and Sokhansanj, 1993; Farid, 1994).

Four annual generations, two in winter and two in spring, were observed on weeping fig (Ficus benjamina) in Saudi Arabia, where populations were lowest in summer, probably due to high temperatures (Badawi and Al-Ahmed, 1990). In India, three generations a year were recorded (Glover, 1933).

Crawlers and female scales feed on dilute sap and surplus carbohydrate and nitrogen is converted into material to construct the scale cover, and not into honeydew as in other scale insect families.

Natural enemies

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Natural enemyTypeLife stagesSpecificityReferencesBiological control inBiological control on
Ablerus aonidiellae Parasite Adults/Nymphs
Anagyrus pseudococci Parasite
Aphytis aonidiae Parasite
Aphytis lingnanensis Parasite
Aphytis melinus Parasite Adults/Nymphs
Aphytis philippinensis Parasite Adults/Nymphs India; Karnataka; Tamil Nadu Calotropis gigantea; Securinega virosa
Aphytis riyadhi Parasite Adults/Nymphs
Arrhenophagus chionaspidis Parasite
Azotus bharathius Parasite Adults/Nymphs
Azotus fumipennis Parasite Adults/Nymphs
Chilocorus baileyii Predator Adults/Nymphs
Chilocorus circumdatus Predator Adults/Nymphs
Chilocorus nigrita Predator Adults/Nymphs
Chilocorus renipustulatus Predator Adults/Nymphs
Coccobius aligarhensis Parasite Adults/Nymphs
Coccobius reticulatus Parasite Adults/Nymphs
Coccophagoides orientalis Parasite Adults/Nymphs
Coccophagus ceroplastae Parasite Adults/Nymphs
Comperiella bifasciata Predator/parasite Adults/Nymphs
Comperiella indica Parasite
Comperiella lemniscata Predator/parasite Adults/Nymphs
Encarsia aurantii Parasite Adults/Nymphs
Encarsia citrina Parasite Adults/Eggs/Nymphs
Habrolepis rouxi Parasite
Marietta leopardina Parasite Adults/Nymphs
Marlattiella maculata Parasite Adults/Nymphs
Pharoscymnus horni Predator Adults/Nymphs
Pharoscymnus simmondsi Predator Adults/Nymphs
Physcus gunturensis Parasite Adults/Nymphs
Promuscidea unfasciativentris Parasite Adults/Nymphs
Sticholotis marginalis Predator Adults/Nymphs
Thomsonisca amathus Parasite

Notes on Natural Enemies

Top of page Although A. orientalis has a wide distribution, its natural enemies have only been reported from a few countries, most notably India, Pakistan and Saudi Arabia (Rajagopal and Krishnamoorthy, 1996). In India, natural enemies were identified on a range of crops by Mani and Krishnamoorthy (1996). They recorded A. orientalis being parasitized by species of Aphytis on banana and custard apple (Annona reticulata), for example, but levels of parasitism were generally low.

Hayat (1986) listed a number of other parasitoids known to attack A. orientalis in the families Encyrtidae and Aphelinidae. Comperiella bifasciata and C. lemniscata are probably the only two parasitoids that are naturally effective at checking populations of A. orientalis over most of its range (Rajagopal and Krishnamoorthy, 1996).

Coccinellid beetles and lacewings are frequent predators of A. orientalis in a variety of crops (Mani and Krishnamoorthy, 1996).

Hyperparasites of the most common parasites of A. orientalis include Ablerus spp., Azotus spp., Marietta spp. and Zaomma spp. (Ofek et al., 1997).


Top of page A. orientalis is highly polyphagous and is therefore potentially a serious pest of a wide range of crops. It is considered to be a serious pest in certain areas of the world, notably on coconut and arecanut in South India (Rajagopal and Krishnamoorthy, 1996), and on coconut in Florida, USA (Dekle and Merrill, 1976).

The greatest economic impact attributed to A. orientalis is often in areas it has recently invaded. In Australia, for example, A. orientalis first spread from the Torres Strait Islands to Queensland in 1956. It caused problems for the first time in papaya during 1988, and is now the most important pest on papaya in northern Queensland (Elder et al., 1998).

It is an important pest of tamarind trees in India (Rajagopal and Krishnamoorthy, 1996), and of species of Citrus (especially Omani lime, sweet lime and grapefruit) in Iran (Farid, 1994) and Asia (Rosen, 1990). It is also a serious pest on coconuts in Malaysia and Sri Lanka, mango in the Philippines and Israel, papaya in Malaysia and Australia, and guava in India (Rosen, 1990). In Nigeria, Niger and northern Cameroon, A. orientalis infestations damage neem (Azadirachta indica) and can kill trees (Boa, 1995).

A. orientalis disrupts lac production, a resinous secretion from the insect Laccifer lacca collected in India and Indonesia, by feeding on the same hosts and thereby decreasing the purity and yield of the product (Rajagopal and Krishnamoorthy, 1996).

Detection and Inspection

Top of page Look for circular, flat, pale-yellow to reddish-brown scales on leaves, but sometimes on branches, trunks, shoots and fruits of host plants.

Similarities to Other Species/Conditions

Top of page A. orientalis is easily distinguished from most other Aonidiella species as the adult female's body is less heavily sclerotized and fails to become strongly reniform at maturity. It also has conspicuous submarginal groups of macroducts on either side of the free abdominal segments. However, it is similar to A. simplex and A. andersoni, although both these species lack perivulvar pores, which are present in A. orientalis females (McKenzie, 1938).

Prevention and Control

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Cultural Control

The pruning of lower stalks and water management can be useful in controlling A. orientalis (Khalaf and Sokhansanj, 1993) in Iran. In India, the cutting and burning of damaged shoots can keep A. orientalis populations under control in ber (Ziziphus mauritiana), whereas the removal and destruction of damaged tree parts can aid control during the early stages of infestation in tamarind (Rajagopal and Krishnamoorthy, 1996).

Damaging infestations on neem in West Africa are associated with water stress (Boa, 1995).

Biological Control

A. orientalis has been successfully controlled by three parasitoids on papaya in Queensland, Australia. Comperiella lemniscata was introduced from Hainan Island in China and from the Torres Strait in northern Queensland, and released during 1991. Within 12 months, parasitism rates rose as high as 80% and rejection of fruit for market dropped from 20-30 to 1-2%. Aphytis melinus was also augmentatively released and rates of parasitism were increased, although this parasitoid had to be continually re-released. Encarsia citrina occurred naturally, producing levels of up to 80% parasitism, and was also therefore important in the biological control of A. orientalis (Elder et al., 1998).

C. lemniscata and two predatory coccinellids, Chilocorus circumdatus and C. baileyii, were introduced into Israel from Australia for the control of A. orientalis on mango (Ofek et al., 1997). Rajagopal and Krishnamoorthy (1996) indicated the potential of the parasite Comperiella bifasciata and the predator Chilocorus nigrita as biological control agents.

Chemical Control

The usual chemical treatment is mineral oil sprays (Khalaf and Sokhansanj, 1993), although these are not routinely recommended as they interfere with the natural biological control of pest insects in orchards and plantations. Malathion, dimethoate or diazinon have also previously been recommended for dealing with severe infestations in papaya, tamarind and other crops (Rajagopal and Krishnamoorthy, 1996).


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Arriola Padilla VJ; Estrada Martínez E; Romero Nápoles J; González Hernández H; Pérez Miranda R, 2016. Scale insects (Hemiptera: Coccomorpha) on ornamental plants in greenhouses from the central zone of the Morelos state, Mexico. (Insectos escama (Hemiptera: Coccomorpha) en plantas ornamentales en viveros de la zona centro del estado de Morelos, México.) Interciencia, 41(8):552-560.

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Boa ER, 1995. A guide to the identification of diseases and pests of neem (Azadirachta indica). RAP Publication 1995/41. Bangkok, Thailand, FAO, 16-20, 34, 71 pp.

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Costa EM; Godoy MS; Araujo EL; Silva RIR; Wolff VRdos S, 2013. First report of the infestation of Azadirachta indica A. Juss by Aonidiella orientalis (Newstead) (Hemiptera: Diaspididae) in Brazil. Bioscience Journal, 29(Supplement 1):1441-1445.

Dekle GW; Merrill GB, 1976. Florida armored scale insects. Arthropods of Florida and Neighbouring Land Areas No. 3. Gainesville, USA: Florida Department of Agriculture and Consumer Services, 32, 345 pp.

Elder RJ; Smith D, 1995. Mass rearing of Aonidiella orientalis (Newstead) (Hemiptera: Diaspididae) on butternut gramma. Journal of the Australian Entomological Society, 34(3):253-254; 6 ref.

Elder RJ; Smith D; Bell KL, 1998. Successful parasitoid control of Aonidiella orientalis (Newstead) (Hemiptera: Diaspididae) on Carica papaya L. Australian Journal of Entomology, 37(1):74-79; 11 ref.

Elwan AA, 2000. Survey of the insect and mite pests associated with date palm trees in Al-Dakhliya region, Sultanate of Oman. Egyptian Journal of Agricultural Research, 78(2):653-664.

Farid A, 1994. Study on bio-ecology and control of Aonidiella orientalis in Jiroft and Hormozgan. Applied Entomology and Phytopathology, 61(1/2):29, 96-105.

Glover PM, 1933. Aspidiotus (Furcaspis) orientalis Newstead, its economic importance in lac cultivation and its control. Indian Lac Research Institute Bulletin, 16:1-22.

Hayat M, 1986. Chalidoidea hosts. Host parasite list. Oriental Insects, 20:323-383.

Khalaf J; Sokhansanj M, 1993. Bioecological studies on orientalis yellow scale (Aonidiella orientalis New.) and its control by integrated methods in Fars province. Applied Entomology and Phytopathology, 60(1/2):53-59 (Persian), 11-12 (English).

Mani M; Krishnamoorthy A, 1996. Aonidiella orientalis (Newstead) (Diaspididae, Homoptera) and its natural enemies found on sapota, ber, custard apple and banana. Entomon, 21(3/4):273-274; 7 ref.

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Ofek G; Huberman G; Yzhar Y; Wysoki M; Kuzlitzky W; Reneh S; Inbal Z, 1997. The control of the oriental red scale, Aonidiella orientalis Newstead and the California red scale, A. aurantii (Maskell) (Homoptera: Diaspididae) in mango orchards in Hevel Habsor (Israel). Alon Hanotea, 51(5):212-218; 8 ref.

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Shalaby FF; Hafez AA; Hamed AR; Morsi GA, 2000. Description and biological studies on Aspidiotiphagus citrinus Craw. (Aphelinidae: Hymenoptera) a new record parasitoid on Aonidiella orientalis (Newst.) in Egypt. Annals of Agricultural Science, Moshtohor, 38(1):531-544.

Verma SP; Dinabandhoo CL, 2005. Armoured scales (Homoptera: Diaspididae) associated with temperate and subtropical fruit trees in Himachal Pradesh. Acta Horticulturae, 696:423-426.

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Wysoki M, 1997. Present status of arthropod fauna in mango orchards in Israel. In: Lavi U, Degani C, Gazit S, Lahav E, Pesis E, Prusky D, Tomer E, Wysoki M, eds. Proceedings of the 5th International Mango Symposium, Volume 2. Acta Horticulturae, 455:805-811.

Distribution Maps

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