The Featured Creatures collection provides in-depth profiles of insects, nematodes, arachnids and other organisms relevant to Florida. These profiles are intended for the use of interested laypersons with some knowledge of biology as well as academic audiences.
The Asian citrus psyllid, Diaphorina citri Kuwayama, is widely distributed in southern Asia. It is an important pest of citrus in several countries as it is a vector of a serious citrus disease called greening disease or Huanglongbing. This disease is responsible for the destruction of several citrus industries in Asia and Africa (Manjunath 2008). Until recently, the Asian citrus psyllid did not occur in North America or Hawaii, but was reported in Brazil, by Costa Lima (1942) and Catling (1970).
In June 1998, the insect was detected on the east coast of Florida, from Broward to St. Lucie counties, and was apparently limited to dooryard host plantings at the time of its discovery. By September 2000, this pest had spread to 31 Florida counties.
Diaphorina citri is often referred to as citrus psylla, but this is the same common name sometimes applied to Trioza erytreae (Del Guercio), the psyllid pest of citrus in Africa. To avoid confusion, T. erytreae should be referred to as the African citrus psyllid or the two-spotted citrus psyllid (the latter name is in reference to a pair of spots on the base of the abdomen in late stage nymphs). These two psyllids are the only known vectors of the etiologic agent of citrus greening disease (Huanglongbing), and are the only economically important psyllid species on citrus in the world. Six other species of Diaphorina are reported on citrus, but these are non-vector species of relatively little importance (Halbert and Manjunath 2004).
Diaphorina citri ranges primarily in tropical and subtropical Asia and is reported from the following geographical areas: Afghanistan, Caribbean (Bahamas, the Cayman Islands, Jamaica, Dominican Republic, Cuba, and Puerto Rico, plus interceptions from St. Thomas and Belize), Central America (Guadaloupe), China, Hong Kong, India, Indonesia, Malaysia, Mauritius, Mexico, Myanmar, Nepal, Pakistan, Philippine Islands, Reunion Island, Ryukyu Islands, Saudi Arabia, Sri Lanka, South America (Argentia, Brazil, Venezuela), Taiwan, Thailand, and the United States and some of its territories (Halbert and Núñez 2004a).
The discovery of D. citri in Saudi Arabia (Wooler et al. 1974) was the first record from the Near East. Trioza erytreae also occurs in Saudi Arabia, preferring the eastern and highland areas where the extremes of climate are present, whereas D. citri is widespread in the western, more temperate coastal areas.
In the U.S. and its territories, this species is present in Alabama, Arizona, California, Florida, Georgia, Guam, Hawaii, Louisiana, Mississippi, Puerto Rico, South Carolina, Texas, and the U.S. Virgin Islands. In late May 2008, specimens were discovered in Jefferson and Orleans Parishes, Louisiana. On September 2, 2008, the psyllid was first detected in San Diego County, California. On October 27, 2009, the psyllid was discovered in Yuma County, Arizona. On April 21, 2010, surveys determined that the psyllid was present in the U.S. Virgin Islands (USDA 2010a).
As of June 2010, the following U.S. areas are quarantined due to the presence of the Asian citrus psyllid (USDA 2010b):
- Alabama: entire state
- Arizona: portion of Yuma County (USDA 2010a)
- California: southern areas (USDA 2010b)
- Florida: entire state
- Georgia: entire state
- Guam: entire territory
- Hawaii: entire state
- Louisiana: entire state
- Mississippi: entire state
- Puerto Rico: entire commonwealth.
- South Carolina: southeastern area
- Texas: entire state
- Virgin Islands - entire Territory (USDA 2010a)
Description and Identification
The adults are 3 to 4 mm long with a mottled brown body. The head is light brown, whereas T. erytreae has black head. The forewing is broadest in the apical half, mottled, and with a brown band extending around the periphery of the outer half of the wing. This band is slightly interrupted near the apex (in T. erytreae, band is broadest at middle, unspotted and transparent). The antennae have black tips with two small, light brown spots on the middle segments (in T. erytreae, antennae are nearly all black). A living D. citri is covered with whitish, waxy secretion, making it appear dusty.
Diaphorina citri nymphs are 0.25 mm long during the 1st instar, and 1.5 to 1.7 mm in last (5th) instar. Their color is generally yellowish-orange. There are no abdominal spots, whereas in T. erytreae, advanced nymphs have two basal dark abdominal spots. The wing pads in D. citri are large, while T. erytreae has small pads. In D. citri, large filaments are confined to the apical plate of the abdomen (in T. erytreae, there is a fringe of fine white filaments around the whole body, including head).
The eggs of D. citri are approximately 0.3 mm long, elongate, almond-shaped, thicker at the base, and tapering toward the distal end. Newly laid eggs are pale, but then turn yellow and finally orange before hatching. The eggs are placed on plant tissue the with long axis vertical to surface. Trioza erytreae eggs are laid with the long axis horizontal to surface.
Identifications having regulatory significance should be made by taxonomists with adequate reference materials. Psyllids as a group are most likely to be confused with aphids as these latter insects are common on tender citrus leaves. But adult psyllids are active jumping insects and aphids are sluggish. In addition, aphids usually have four- to six-segmented antennae, while psyllid antennae usually have 10 segments. Most aphids have cornicles on the abdomen, while psyllids lack cornicles.
Eggs are laid on tips of growing shoots on and between unfurling leaves. Females may lay more than 800 eggs during their lives. Nymphs pass through five instars. The total life cycle requires from 15 to 47 days, depending upon the season. Adults may live for several months. There is no diapause, but populations are low in winter (the dry season). There are nine to 10 generations a year; however, 16 have been observed in field cages.
Capoor et al. (1974) described greening symptoms of citrus as trees showing stunted growth, sparsely foliated branches, unseasonal bloom, leaf and fruit drop, and twig dieback. Young leaves are chlorotic, with green banding along the major veins. Mature leaves have yellowish-green patches between veins, and midribs are yellow. In severe cases, leaves become chlorotic and have scattered spots of green. Fruits on greened trees are small, generally lopsided, underdeveloped, unevenly colored, hard, and poor in juice. The columella (the internal, central columnlike structure found in citrus and other fruits) was found to be almost always curved in sweet orange fruits and apparently is the most reliable diagnostic symptom of greening. Most seeds in diseased fruits are small and dark colored.
Mainly Citrus spp., at least two species of Murraya, and at least three other genera, all in the family Rutaceae.
Survey and Detection
The nymphs are always found on new growth, and move in a slow, steady manner when disturbed.
The adults leap when disturbed and may fly a short distance. They are usually found in large numbers on the lower sides of the leaves with heads almost touching the surface and the body raised almost to a 30° angle. The period of greatest activity of the psyllid corresponds with the periods of new growth of citrus. There are no galls or pits formed on the leaves as caused by many other kinds of psyllids. The nymphs are completely exposed, while the nymphs of T. erytreae are partially enclosed in a pit. Citrus trees in advanced stages of decline are somewhat similar to those affected by tristeza. Field recognition of greening disease in Asia from symptoms alone is difficult. Very similar leaf symptoms may be caused by a wide variety of factors varying from nutritional disorders to the presence of other diseases such as root rots and gummosis, tristeza, and exocortis.
Huanglongbing (HLB) is caused by a phloem-limited bacterium that has a true cell wall. There are at least three forms or species: Candidatus L. africanus causing African HLB; Candidatus L. asiaticus causing Asian HLB; and a new variant found in Brazil, tentatively called Candidatus L. americanus. Asian HLB is the bacterium found in Florida (Ask IFAS 2021). Capoor et al. (1974) reported a high percentage of transmission by tissue grafts. They found that 4th and 5th instar nymphs and adults could affect transmission. Diaphorina citri requires an incubation period before it can transmit the pathogen, which it retains for life following a short access feeding (15 to 30 minutes) on a diseased plant. Infectious nymphs retain their ability to vector the disease into adulthood. Adult psyllids transmit the pathogen that causes greening after feeding for as little as 15 minutes, but transmission was low. One hundred percent infection was obtained when the psyllids fed for one hour or more. Capoor et al. (1974) indicated that the pathogen multiplied in the body of the psyllid and that there was an absence of transovarial transmission. They summarized differences between D. citri and Trioza erytreae in various aspects of greening transmission.
Workers in India reported that D. citri can be controlled effectively with a wide range of modern insecticides. Injection of trees with tetracycline antibiotics to control greening disease was effective where the vector can be kept under control. In countries where greening spread over long distances, it occurred because of the movement of infected and infested nursery stock. Only clean and healthy plants should be transported. In areas with low incidence of greening disease, the any infected trees should be removed to prevent them from being reservoirs of the pathogen.
Natural enemies of D. citri include syrphids, chrysopids, at least 12 species of coccinellids, and several species of parasitic wasps, the most important of which is Tamarixia radiata (Waterston). T. radiata was introduced in Florida (intentionally) and the Rio Grande Valley of Texas (accidentally) (Michaud, personal communication).
In the United States and its territories, areas with D. citri are under quarantine (USDA 2010a). International quarantines, enacted by other countries, may also be placed on countries with D. citri.
Ask IFAS. (May 2021) Citrus Greening (Huanglongbing, HLB). https://edis.ifas.ufl.edu/entity/topic/citrus_greening.
Atwal AS, Chaudhary JP, Ramzan M. 1970. Studies on the development and field population of citrus psylla, Diaphorina citri Kuwayama (Psyllidae: Homoptera). Journal of Research Punjab Agricultural University 7: 333–338.
Bindra OS, Sohi BS, Batra RC. 1974. Note on the comparative efficacy of some contact and systemic insecticides for the control of citrus psylla in Punjab. Indian Journal of Agricultural Science 43: 1087–1088.
Capoor SP, Rao DG, Viswanath SM. 1974. Greening disease of citrus in the Deccan Trap Country and its relationship with the vector, Diaphorina citri Kuwayama. p. 43–49. In Weathers LG, Cohen M (editor). Proceedings of the 6th Conference of the International Citrus Virology, University of California, Division of Agricultural Sciences.
Catling HD. 1970. Distribution of the psyllid vectors of citrus greening disease, with notes on the biology and bionomics of Diaphorina citri. FAO Plant Protection Bulletin 18: 8–15.
Costa Lima AM. da. 1942. Homopteros. Insetos do Brazil 3: 1–327. Esc. Na. Agron. Min. Agr.
FDACS. (2005). Host plant list for Asian citrus psyllid and citrus greening. Division of Plant Industry. (16 June 2008).
Grafton-Cardwell EE, Godfrey KE, Rogers ME, Childers CC, Stansly PA. (2005). Asian citrus psyllid. https://ccpp.ucr.edu/news/PsyllidbrochureAug05.pdf (16 June 2008).
Halbert SE, Núñez CA. (2004a). Distribution of the Asian citrus psyllid, Diaphorina citri Kuwayama (Rhynchota: Psyllidae), in the Caribbean basin. Florida Entomologist 87 (3). https://journals.flvc.org/flaent/article/view/75325/72983 (1 March 2022).
Halbert SE, Manjunath KL. (2004b). Asian citrus psyllids (Sternooohyncha: Psyllidae) and greening disease of citrus: a literature review and assessment of risk in Florida. Florida Entomologist 87 (3). https://journals.flvc.org/flaent/article/view/75313/72971 (1 March 2022).
Halbert SE. (2006). Asian citrus psyllid - A serious exotic pest of FL citrus. https://www.fdacs.gov/content/download/68181/file/Pest%20Alert%20-%20Diaphorina%20citri,%20Asian%20citrus%20psyllid.pdf
Hall DG. 2006. A closer look at the vector: Controlling the Asian citrus psyllid is the key to managing citrus greening. Citrus & Vegetable Magazine 70 (5): 24–26.
Hall DG, Hentz MG, Adair Jr RC. 2008. Population ecology and phenology of Diaphorina citri (Hemiptera: Psyllidae) in two Florida citrus groves. Environmental Entomology 37: 914–924.
Hoy MA, Nguyen R, Jeyaprakash A. (1999). Classical biological control of Asian citrus psyllid in Florida. Florida IPM. https://ipm.ifas.ufl.edu/Agricultural_IPM/psyllid.shtml (15 May 2014).
Hoy MA, Nguyen R, Jeyaprakash A. (2006). Classical biological control of the citrus leafminer: release of Cirrospilus quadristriatus. Florida IPM. https://ipm.ifas.ufl.edu/Agricultural_IPM/clmhoy8.shtml (15 May 2014).
Husain MA, Nath D. 1927. The citrus psylla (Diaphorina citri, Kuw.) (Psyllidae: Homoptera) Memoirs of the Department of Agriculture India 10: 1–27.
Mangat BS. 1961. Citrus psylla (Diaphorina citri Kuway) and how to control it. Citrus Industry 42: 20.
Manjunath KL, Halbert SE, Ramadugu C, Webb S, Lee RF. (2008). Detection of 'Candidatus Liberibacter asiaticus' in Diaphorina citri and its importance in the management of citrus Huanglongbing in Florida. Phytopathology 98. https://apsjournals.apsnet.org/doi/10.1094/PHYTO-98-4-0387
Mathur RN. 1975. Psyllidae of the Indian Subcontinent. Indian Council of Agricultural Research, New Delhi. 429 pp.
Michaud JP. Personal communication. (19 October 2002).
Miyakawa T, Tanaka H, Matsui C. 1974. Studies on citrus greening disease in southern Japan. p. 40–42 In Weathers LG, Cohen M (editor). Proceedings of the 6th Conference of the International Citrus Virology, University of California, Division of Agricultural Sciences.
Moll JN, van Vuuren SP. 1977. Greening Disease in Africa. 1977 International Citrus Congress, Orlando, Florida, Program and Abstracts. 95 pp.
Pande YD. 1971. Biology of citrus psylla, Diaphorina citri Kuw. (Hemiptera: Psyllidae). Israel Journal of Entomology 6: 307-310.
Raychaudhuri SP, Nariani, Ghosh SK, Viswanath SM, Kumar D. 1974. Recent studies on citrus greening in India. p. 53-57. In Weathers LG, Cohen M (editor). Proceedings of the 6th Conference of the International Citrus Virology, University of California, Division of Agricultural Sciences.
Schwarz RE, Knorr LC, Prommintara M. 1974. Citrus greening disease in Thailand FAO Technical Document No. 93: 1-14.
USDA. 1959. Insects not known to occur in the United States. Citrus psylla (Diaphorina citri Kuwayama). No. 88 of Series. Cooperative Economic Insect Report 9: 593–594.
USDA. (2008). Citrus Greening. Plant Health. https://www.aphis.usda.gov/aphis/ourfocus/planthealth/plant-pest-and-disease-programs/pests-and-diseases/citrus/citrus-greening (March 2022).
USDA. (February 2009). Area wide control of Asian citrus psyllid (Diaphorina citri) Technical Working Group Report. Plant Health. https://swfrec.ifas.ufl.edu/hlb/database/pdf/00002462.pdf (1 March 2022).
USDA. (May 2010a). Citrus Greening - Regulatory Updates. Plant Health. https://www.aphis.usda.gov/aphis/ourfocus/planthealth/plant-pest-and-disease-programs/pests-and-diseases/citrus/citrus-federal-orders/citrus-quarantine-federal-orders?disease=hlb (May 2021)
USDA. (June 2010b). National Quarantine: Citrus Greening And Asian Citrus Psyllid. Plant Health. https://www.aphis.usda.gov/aphis/maps/plant-health/citrus-map (May 2021)
Wooler A, Padgham D, Arafat A. 1974. Outbreaks and new records. Saudi Arabia. Diaphorina citri on citrus. FAO Plant Protection Bulletin 22: 93–94.