Polyphagotarsonemus latus (broad mite)
Index
- Pictures
- Identity
- Summary of Invasiveness
- Taxonomic Tree
- Description
- Distribution Table
- Hosts/Species Affected
- Host Plants and Other Plants Affected
- Growth Stages
- Symptoms
- List of Symptoms/Signs
- Biology and Ecology
- Natural enemies
- Notes on Natural Enemies
- Impact
- Prevention and Control
- References
- Distribution Maps
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Top of pageIdentity
Top of pagePreferred Scientific Name
- Polyphagotarsonemus latus Banks
Preferred Common Name
- broad mite
Other Scientific Names
- Hemitarsonemus latus Banks
- Hemitarsonemus translucens
- Polyphagotarsonemus translucens
- Tarsonemus latus
- Tarsonemus phaseoli
- Tarsonemus translucens (Green)
International Common Names
- English: chilli mite; citrus silver mite; jute white mite; rubber leaf mite; tropical mite; yellow tea mite
- Spanish: acaro amarillo; acaro blanco tropical; acaro tostador de los cítricos; aranuela blanca
- French: acarien jaune; tarsoneme du cottonnier; tarsoneme trapu
Local Common Names
- Brazil: acaro branco do mamdeiro; acaro tropical
- Denmark: skudtopmide; topskudmide
- Germany: breit-milbe; gelbe tee-milbe; weisse milbe
- Italy: acaro giallo
- Netherlands: begoniamijt; theemijt geele
- Norway: skottopmidd
- Sweden: skott-toppkvalster
EPPO code
- HEMTLA (Polyphagotarsonemus latus)
Summary of Invasiveness
Top of pageThe broad mite P. latus is spread worldwide. In the tropics and subtropics it reproduces the whole year round and has a wide host range. In temperate climates it is a serious pest on vegetables and ornamental plants in glasshouses. Due to its high reproductive potential, it can reach damaging densities within a very short time.
Taxonomic Tree
Top of page- Domain: Eukaryota
- Kingdom: Metazoa
- Phylum: Arthropoda
- Subphylum: Chelicerata
- Class: Arachnida
- Subclass: Acari
- Superorder: Acariformes
- Suborder: Prostigmata
- Family: Tarsonemidae
- Genus: Polyphagotarsonemus
- Species: Polyphagotarsonemus latus
Description
Top of page
Adult females of P. latus are small (ca 200 µm) and have an unornamented dorsal shield. The prodorsal shield is not enlarged to cover the stigmata. Trichobothria on the prodorsum are capitate. Dorsal idiosomal setae are short. There are four pairs of setae on the dorsum of propodosoma in the male. Tibia and tarsus IV of the male are fused and bear a button-like claw.
Lindquist (1986) provided a detailed description and illustration of this species.
Distribution Table
Top of pageThe 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: 21 Jul 2022Continent/Country/Region | Distribution | Last Reported | Origin | First Reported | Invasive | Reference | Notes |
---|---|---|---|---|---|---|---|
Africa |
|||||||
Benin | Present | ||||||
Burkina Faso | Present | ||||||
Burundi | Present | ||||||
Cameroon | Present | ||||||
Central African Republic | Present | ||||||
Chad | Present | ||||||
Côte d'Ivoire | Present | ||||||
Ethiopia | Present | ||||||
Kenya | Present | ||||||
Liberia | Present | ||||||
Mali | Present | ||||||
Mauritius | Present | ||||||
Morocco | Present | ||||||
Mozambique | Present | ||||||
Nigeria | Present | ||||||
Senegal | Present | ||||||
South Africa | Present | ||||||
Sudan | Present | ||||||
Tanzania | Present | ||||||
Uganda | Present | ||||||
Asia |
|||||||
Bangladesh | Present | ||||||
China | Present | ||||||
-Fujian | Present | ||||||
-Guangdong | Present | Original citation: Zhang et al. (1980) | |||||
-Hainan | Present | ||||||
-Shanghai | Present | ||||||
-Sichuan | Present | ||||||
India | Present | ||||||
-Andhra Pradesh | Present | ||||||
-Bihar | Present | ||||||
-Gujarat | Present | ||||||
-Himachal Pradesh | Present | ||||||
-Jharkhand | Present | ||||||
-Karnataka | Present | ||||||
-Maharashtra | Present | ||||||
-Odisha | Present | ||||||
-Punjab | Present | ||||||
-Rajasthan | Present | ||||||
-Tamil Nadu | Present | ||||||
-Uttar Pradesh | Present | ||||||
-West Bengal | Present | ||||||
Indonesia | Present | ||||||
-Java | Present | ||||||
-Sumatra | Present | ||||||
Iran | Present | ||||||
Japan | Present | ||||||
-Honshu | Present | ||||||
-Kyushu | Present | ||||||
Malaysia | Present | ||||||
Myanmar | Present | ||||||
Oman | Present | ||||||
Pakistan | Present | ||||||
Philippines | Present | ||||||
Saudi Arabia | Present | ||||||
Singapore | Present | ||||||
South Korea | Present | ||||||
Sri Lanka | Present | ||||||
Taiwan | Present | ||||||
Thailand | Present | ||||||
Turkey | Present | ||||||
Vietnam | Present | Original citation: Duong-Nguyen Hai et al. (1998) | |||||
Europe |
|||||||
Belgium | Present | ||||||
France | Present | ||||||
Germany | Present | ||||||
Greece | Present | ||||||
Hungary | Present | ||||||
Italy | Present | ||||||
Montenegro | Present | Introduced | Invasive | ||||
Netherlands | Present | ||||||
Norway | Present | ||||||
Poland | Present | Original citation: Labanowski (1999) | |||||
Portugal | Present | ||||||
Romania | Present | ||||||
Serbia | Present | ||||||
Spain | Present | ||||||
Sweden | Present | ||||||
Switzerland | Present | ||||||
United Kingdom | Present | ||||||
North America |
|||||||
Bermuda | Present | ||||||
Canada | Present | Present based on regional distribution. | |||||
-Ontario | Present | ||||||
Costa Rica | Present | ||||||
Cuba | Present | ||||||
Guadeloupe | Present | ||||||
Jamaica | Present | ||||||
Martinique | Present | ||||||
Mexico | Present | ||||||
Nicaragua | Present | ||||||
Panama | Present | ||||||
Puerto Rico | Present | ||||||
Trinidad and Tobago | Present | ||||||
U.S. Virgin Islands | Present | ||||||
United States | Present | ||||||
-Arkansas | Present | ||||||
-California | Present | ||||||
-Connecticut | Present | ||||||
-Florida | Present | ||||||
-Hawaii | Present | ||||||
-Illinois | Present | ||||||
-Louisiana | Present | ||||||
-Maryland | Present | ||||||
-New York | Present | ||||||
-Pennsylvania | Present | ||||||
-Virginia | Present | ||||||
-Washington | Present | ||||||
Oceania |
|||||||
Australia | Present | ||||||
-New South Wales | Present | ||||||
-Queensland | Present | ||||||
-Western Australia | Present | ||||||
Fiji | Present | ||||||
Guam | Present | ||||||
New Zealand | Present | ||||||
Papua New Guinea | Present | ||||||
Samoa | Present | ||||||
Solomon Islands | Present | ||||||
South America |
|||||||
Argentina | Present | ||||||
Brazil | Present | ||||||
-Bahia | Present | ||||||
-Ceara | Present | ||||||
-Distrito Federal | Present | ||||||
-Espirito Santo | Present | ||||||
-Pernambuco | Present | ||||||
-Rio de Janeiro | Present | ||||||
-Rio Grande do Sul | Present | ||||||
-Santa Catarina | Present | ||||||
-Sao Paulo | Present | ||||||
Colombia | Present | ||||||
Guyana | Present | ||||||
Peru | Present | ||||||
Venezuela | Present |
Hosts/Species Affected
Top of pageHost Plants and Other Plants Affected
Top of pageSymptoms
Top of pageP. latus symptoms vary on different plants (Gerson, 1992). Edges of damaged young leaves usually curl. The foliage often becomes rigid and appears bronzed or scorched. Feeding of mites on the under surface of young leaves causes Gerbera to become rigid and rolled under at the edges. As leaves age, they may split, producing a ragged appearance of different shapes. Infested young potato leaves initially have oily black spots on the under surface, which later turn reddish. The plants become rosetted and then die back. Symptoms on red chilli pepper (Capsicum sp.) are similar. On lemons, this species produces multiple buds on citrus seedlings and discoloration on the skin of fruit. Damage on cucumber, aubergines and Solanum laciniatum includes crinkling, cracking, discoloration and malformations similar to those caused by a hormonal weedkiller. When grapevine is attacked, young leaf edges turn downwards, followed by browning and necrosis.
When chilli leaves are attacked, the leaf tissues disintegrate and the epidermal layer of the infested leaves thickens, with both the pallisade and spongy parenchymatous tissues becoming irregular and the cell nuclei enlarged in severely infested leaves (Karmakar, 1997).
List of Symptoms/Signs
Top of pageSign | Life Stages | Type |
---|---|---|
Fruit / abnormal shape | ||
Fruit / discoloration | ||
Growing point / distortion | ||
Inflorescence / discoloration panicle | ||
Inflorescence / twisting and distortion | ||
Inflorescence / wilt | ||
Leaves / abnormal colours | ||
Leaves / abnormal forms | ||
Leaves / abnormal forms | ||
Leaves / necrotic areas | ||
Leaves / necrotic areas | ||
Leaves / wilting | ||
Stems / stunting or rosetting | ||
Whole plant / plant dead; dieback |
Biology and Ecology
Top of page
The generation time of P. latus is short. On chilli pepper (Capsicum sp.) the developmental period from egg to adult at 25°C averages 4.1 days for both males and females. Adult female and male longevity is 11.4 and 15.3 days, respectively. Each female lays 25 eggs. The female/male sex ratio is 2.8 in the laboratory, and 2.3 on seedlings in the greenhouse (Ho, 1991).
P. latus eggs are laid on the underside of leaves, tender stems, fruits, flower peduncles and flowers. Attack occurs during a short period of time. Discoloration of tissues is produced by mite feeding; fruits become deformed or fail to develop. Severely infected fruits fall. Leaves of attacked plants are stunted and yield is significantly reduced. Symptoms remain for a long period of time after control.
P. latus disperses by various means. Short-distance movement may be accomplished by walking. Mites may reach far-away uninfested plants by wind. Human transport of infested plants is another way of dispersal for this mite.
There is also evidence that P. latus disperses through insects living on plants. Females of P. latus were observed to have a phoretic relationship with Bemisia tabaci on Phaseolus vulgaris in Colombia and on watermelons in Venezuela. Females of P. latus were found attached to the tarsi and tibiae of B. tabaci (Flechtmann et al., 1990) and B. argentifolii (Fan and Petitt, 1998). The phoretic association between P. latus and insects is quite specific; whiteflies are most attractive to P. latus but other insects such as thrips and aphids are rarely used (Palevsky et al., 2001).
Natural enemies
Top of pageNatural enemy | Type | Life stages | Specificity | References | Biological control in | Biological control on |
---|---|---|---|---|---|---|
Amblyseius agrestis | Predator | |||||
Amblyseius barkeri | Predator | Florida | ||||
Amblyseius degenerans | Predator | |||||
Amblyseius delhiensis | Predator | |||||
Amblyseius largoensis | Predator | |||||
Amblyseius limonicus | Predator | |||||
Amblyseius nicholsi | Predator | |||||
Amblyseius peregrinus | Predator | |||||
Amblyseius victoriensis | Predator | Australia; Queensland | Citrus | |||
Beauveria bassiana | Pathogen | |||||
Euseius concordis | Predator | |||||
Euseius hibisci | Predator | |||||
Euseius ovalis | Predator | Eggs; Arthropods|Larvae | ||||
Euseius stipulatus | Predator | |||||
Galendromus annectens | Predator | |||||
Hirsutella thompsonii | Pathogen | |||||
Metaseiulus occidentalis | Predator | |||||
Neoseiulus californicus | Predator | |||||
Neoseiulus cucumeris | Predator | |||||
Paecilomyces fumosoroseus | Pathogen | |||||
Typhlodromus porresi | Predator | |||||
Typhlodromus rickeri | Predator |
Notes on Natural Enemies
Top of pageWaterhouse and Norris (1987) discussed the natural enemy records and pointed out that none are specific to P. latus. They recommended biological control experiments using Typhlodromus stipulatus and Amblyseius ovalis on chilli peppers.
Impact
Top of pageP. latus is a serious pest of tea, chilli pepper and aubergines in China (Li et al., 1985). It was reported to have destroyed 50% of the bean crop in New Guinea and of the lemon crop in parts of South Africa. It is a pest of cotton in tropical Africa and Brazil. It has a worldwide distribution on many crops (Gerson, 1992).
Damage by P. latus was 100% on sweet peppers (Capsicum sp.) grown in a screenhouse in Taiwan, while aubergines, Datura, chilli pepper and Gerbera were severely damaged (Liu et al., 1991).
Prevention and Control
Top of pageDue 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.
Chemical Control
P. latus may be difficult to control on certain plants. On the curly leaves of Psophocarpus tetragonolobus, dicofol, bromopropylate, azocyclotin and abamectin were not effective (Heungen and Degheele, 1986), presumably because the mites were protected in curly leaves; chinomethionat was more effective. On the more easily treated leaves of castor, all five pesticides tested virtually eliminated the mite population in 2 weeks, and abamectin remained effective for up to 3 weeks.
Dicofol and wettable sulphur were effective against all life stages of P. latus on chilli (Karmakar et al., 1996).
In Sao Paulo, Brazil, abamectin was the most efficient acaricide against P. latus in 12 applications at a range of rates and one application at a higher rate; the higher rate application maximized the production of beans (Scarpellini, 1999). Chlorfenapyr is recommended for the control of P. latus on cotton in Sao Paulo (Santos et al., 1999).
Greenhouse tests in China showed that liuyangmycin (an antibiotic preparation from Streptomyces griseolus) gave the most effective and economical control of P. latus on green chilli peppers (Capsicum). Introduction of female adults or nymphs to plants 5 days after treatment with liuyangmycin resulted in 71.1 and 83% mortality, respectively. The effect declined after 7 days, but mite control for the 3 weeks after treatment remained >98%, which was equivalent to a control by dicofol (Xie et al., 1992). Three applications liuyangmycin to Capsicum in the greenhouse in September-April gave satisfactory control of the pest, with no side-effects.
In India, leaf extracts of Lippia nodiflora and Aloe sp. were shown to significantly reduce the population density of P. latus on chilli when sprayed as 5% aqueous extracts (Palaniswamy and Ragini, 2000). In Brazil, Manipueira, a liquid extract from cassava roots, provided 100% control of P. latus on papaya plants when it was diluted in water (1:3) and sprayed three times at weekly intervals (Ponte, 1996).
Biological Control
In laboratory tests with chilli (Capsicum annuum) leaves, Amblyseius ovalis [Euseius ovalis] at predator-prey ratios of 1:25, 1:50 and 1:100 eliminated P. latus after 9, 12 and 17 days, respectively. Moutia (1958) reported similar results from Mauritius.
In the greenhouses in the 'Land' section of the EPCOT Center, Walt Disney World Vacation Resort, Florida, P. latus was controlled by releasing Neoseiulus barkeri. Fan and Petitt (1994) showed that releasing 10 or more predatory mites per plant of Capsicum cv. Hungarian Wax effectively reduced populations of P. latus from more than 100 mites per leaf to zero in a week. Influx experiments, in which there was continuous immigration of P. latus, showed that a single release of five N. barkeri adults per plant significantly reduced populations of P. latus, but failed to prevent all plants from mite injury, and that three releases of five predatory mites per main stem every 7 days provided adequate protection from mite injury for over 7 weeks.
On beans (Phaseolus vulgaris) and limes in greenhouses in Florida, USA, Neoseiulus californicus was more effective than N. barkeri. In the field, N. californicus, together with a complex of indigenous predaceous mites, kept the density of P. latus below economically damaging levels on lime fruits (Pena and Osborne, 1996).
In greenhouses in China, the release of predatory mites of Neoseiulus cucumeris successfully controlled P. latus on sweet pepper (Wang et al., 2000).
Several species of fungi were tested as possible biocontrol agents against P. latus (Pena et al., 1996). Mortality of P. latus caused by Beauveria bassiana occurred fastest at densities fluctuating between 65 and 125 mites per leaf.
Host-Plant Resistance
Plant resistance is not yet employed as a component in broad mite (P. latus) control, but there is some evidence that the potential exists (Gerson, 1992). In Cuba, a double haploid of sweet pepper (Capsicum sp.) that has higher mean fruit weight and yield per plant was tolerant of P. latus (Depestre and Gomez, 1995). Several chilli cultivars in India are resistant to P. latus (Rao and Ahmed, 2001).
References
Top of pageBulut E, Gocmen H, Albajes R, Sekeroglu E, 2000. Pests and their natural enemies on greenhouse vegetables in Antalya. Bulletin OILB SROP, 23:33-37
Cho MR, Jeon HY, La SY, Kim DS, Yiem MS, 1996. Damage of broad mite, Polyphagotarsonemus latus (Banks), on pepper growth and yield and its chemical control. Korean Journal of Applied Entomology, 35:326-331
CIE, 1986. Distribution Maps of Plant Pests, No. 191. Wallingford, UK: CAB International
Das LK, Singh B, 1998. Integrated management of jute pests. Environment and Ecology, 16:218-219
Depestre T, Gomez O, 1995. New sweet pepper cultivars for Cuban off season production. Capsicum & Eggplant Newsletter. No. 14, 47-49
Dhandapani N, Kumaraswami T, 1985. Persistence of toxicity in some foliar insecticides against sucking pests in chillies. Indian Journal of Plant Protection, 11:20-23
Gupta SK, 1985. Handbook on Mites of India. Calcutta, India: Zoological Survey of India
Kalshoven LGE, 1950. The Pests of Cultivated Plants in Indonesia. Part 1. The Hague, Netherlands: W. van Hoeve
Kalshoven LGE, 1950. The Pests of Cultivated Plants in Indonesia. Part 1. The Hague, Netherlands: W. van Hoeve
Moutia LA, 1958. Contribution to the study of some phytophagous Acarina and their predators in Mauritius. Bulletin of Entomological Research, 49:59-75
Rao PP, Ahmed K, 2001. Resistance in chilli cultivars to yellow mite, Polyphagotarsonemus latus banks. Indian Journal of Agricultural Research, 35:95-99
Song, S., Qi, S., 1995. Investigation of Tetranychus cuspidatum Pest Damage on Tea Plant and Pharmacological Control Experiment. Fujian Agricultural Science and Technology, 6
Wang DS, Kuang KY, Wu SC, Zhu ZY, Yuan YD, Chen YL, Yang XQ, 2000. The occurrence and control of dominant insect pests and diseases on sweet pepper in advanced greenhouses. Acta Agriculturae Shanghai, 16(Supplement):10-16
Waterhouse DF, Norris KR, 1987. Biological control: Pacific prospects. viii + 454pp
Yang QH, Chen CX, 1982. A study on Polyphagotarsonemus latus Banks. Kunchong Zhishi, 19(2):24-26
Distribution References
CABI, Undated. Compendium record. Wallingford, UK: CABI
CABI, Undated a. CABI Compendium: Status inferred from regional distribution. Wallingford, UK: CABI
CABI, Undated b. CABI Compendium: Status as determined by CABI editor. Wallingford, UK: CABI
Dhandapani N, Kumaraswami T, 1985. Persistence of toxicity in some foliar insecticides against sucking pests in chillies. In: Indian Journal of Plant Protection, 11 20-23.
Gupta SK, 1985. Handbook Plant Mites of India., Calcutta, India: Zoological Survey of India.
Song S, Qi S, 1995. Investigation of Tetranychus cuspidatum Pest Damage on Tea Plant and Pharmacological Control Experiment. Fujian Agricultural Science and Technology.
Distribution Maps
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