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. 2010 Mar 23;10:23. doi: 10.1673/031.010.2301

Occurrence of the Tamarix Leafhopper, Opsius stactogalus Fieber (Hemiptera: Cicadellidae), in Argentina

Eduardo G Virla 1,a*, Guillermo A Logarzo 2,b, Susana L Paradell 3,c
PMCID: PMC3014760  PMID: 20578887

Abstract

The paleartic tamarix leafhopper, Opsius stactogalus Fieber (Hemiptera: Cicadellidae), can reduce the growth of tamarisk due to the aggregate feeding imposed by their populations. The species was mentioned for Argentina in Metcalf's catalogue (1967) without locality or region reference, and the contributions on Cicadellidae published by many authors after Metcalf omitted this distributional data. Populations of O. stactogalus on Tamarix sp. were found in 12 sites between 28° 48′ to 39° 17′ S and 64° 06′ to 70° 04′ W, located in both the Neotropical and Andean biogeographic regions.

Keywords: distribution, Tamarix, tamarisk leafhopper, invasive species

Introduction

Species of Tamarix (Caryophyallales: Tamaricaceae) are native of Eurasia and Africa and, due to their extraordinary biological features and adaptive capabilities (Fornasari 2004), have been introduced and established in 44 countries throughout the world.

At least four species of Tamarix (T. gallica, T. ramosissima, T. chinensis and T. parviflora) and their hybrids occur in Argentina (Gaskin and Schaal 2003; Natale et al. 2008). They were introduced to cover human necessities, mostly as windbreaks, to fix dunes, to control soil erosion, to supply shade, and in some desert places tamarisks are the lone surviving woody plants (León 2006).

However, tamarisk is now an alien plant that invaded the Pampean grasslands, mostly in coastal dunes or in riparian habitats, where it is more invasive, spreading over natural or semi-natural ecosystems (Zalba and Villamil 2002). In addition, tamarisk became a noxious weed in Llancanelo and Guanacache lagoons, both protected RAMSAR sites in Cuyo region, because its invasiveness produces soil salinization, water obstructions, and habitat modifications altering the riparian/wetland trophic structure (Sosa 2003). Consequences of tamarisk's invasiveness, such as water uptake and low diversity of dependent wildlife, have made it the target of classical biological control in the United States (Fornasari 1997, 2004).

Few insects are cited as affecting Tamarix spp. in Argentina: Ceroplastes sp., C. formicarius Hempel and Coccus hesperidum (L.) (Hem: Coccidae), Automeris aspersa (Felder) (Lep: Saturniidae), Oiketicus platensis Berg (Lep: Psychidae), Bostrichopsis uncinata Germ. (Col: Bostrichidae), and Praxithea deroudei (Chabrillac) (Col: Cerambicidae)(Cordo et al. 2004).

Methods and Materials

The geographic range of wild populations of Tamarix spp. cover most of Argentina, except the northeast (Natale et al. 2008). Seven out of 12 provinces where Tamarix spp occurs were surveyed. All the specimens were collected using entomological nets and manual aspirators. Specific identification was made using the keys provided by Oman (1936) and Linnavuori (1959), using both external and male genitalia's characters. Voucher specimens of O. stactogalus resulting from this study are deposited in the collections of the Museo de Ciencias Naturales de La Plata, Buenos Aires (MLPA) and Fundación e Instituto Miguel Lillo at San Miguel de Tucumán (IMLA), Argentina.

Results

Gonatocerus tuberculifemur Ogloblin (Hym: Mymaridae) is an egg parasitoid candidate for the control of Homalodisca vitripennis (Hem: Cicadellidae) in the United States (Jones et al. 2005). During the process of selecting leafhopper species for the study of their host range, abundant populations of a small leafhopper were found on Tamarix sp. in several sites in the Pampas and Monte provinces (Neotropical region, Chacoan subregion), and central and subandean patagonia provinces (Andean region, patagonian subregion) (sensu Morrone 2001); it was identified as the Holartic species Opsius stactogalus Fieber, 1866 (Hemiptera: Cicadellidae) known as the “Tamarix leafhopper”.

Opsius stactogalus (Deltocephalinae: Opsiini) is a leafhopper native to Europe and is strongly associated with the shrubby tree tamarisk (Wiesenborn 2001, 2002). The distribution is primarily Paleartic, but now nearly cosmopolitan, and always associated with tamarisk. Linnavouri & De Long (1977) found this species associated with Casuarina sp. in Chile. This species was previously mentioned by Metcalf (1967) for “Argentina” without locality or region reference, but the known distribution that was published by several authors subsequent to the Metcalf catalogue (Linnavuori 1959; Linnavouri and De Long 1977; Evans 1977; Oman et al. 1990; Zanol 2006) did not mention Argentina. The Tamarix leafhopper is a sap-feeder, and the aggregate feeding imposed by their populations can reduce tamarisk's growth (Liesner 1971, as cited by Wiesenborn 2002). Given the plant's pervasiveness and its undesirable qualities, new distributional data were obtained.

Examined material

ARGENTINA: Rio Colorado (Rio Negro province) (38° 59′ 45.1 S 64° 06′ 07.6 W, elevation: 91 MASL), 21.II.07, 3 females, 1 nymph, Virla & Logarzo cols. (MLPA); Choele Choel (Rio Negro prov.) (39° 17′ 22.6 S 65° 40′ 07.4 W, 126 MASL), 4 females, 1 male, Virla & Logarzo cols. (MLPA); Chimpay (Rio Negro prov.) (39° 10′ 08.7 S 66° 08′ 48.8 W, 154 MASL), 22.II.07, 3 females, 2 males, Virla & Logarzo cols. (MLPA); Neuquén city (Neuquén prov.) (38° 57′ 18.2 S 68° 08′ 42.9 W, 274 MASL), 22.II.07, 5 males, 3 females, 2 nymphs, Virla & Logarzo cols. (MLPA); Zapala (Neuquén prov.) (38° 59′ 4 S 70° 04′ 5 W, 1020 MASL), 10.II.08, 2 females, 4 males, 2 nymphs, Virla col. (IMLA); Villa E1 Chocón (Neuquén prov.) (39° 15′ 43.4 S 68° 46′ 39.1 W, 412 MASL), 02.II.08, 3 females, 3 nymphs, Virla col. (IMLA); Santa Isabel (La Pampa prov.) (36° 22′ 27.2 S 67° 04′ 06.8 W, 303 MASL), 18.II.08, 3 males, 10 females, Logarzo col. (IMLA); Algarrobo del Aguila (La Pampa prov.) (36° 24′ 23.9 S 67° 08′ 22.3 W, 301 MASL), 10.II.08, 2 males, 1 female, 1 nymph, Virla col. (IMLA); San Rafael (Mendoza prov.) (34° 45′ 51 S 68° 24′ 41.4 W, 674 MASL), 11–12.II.08, 8 males, 12 females, 14 nymphs, Virla col. (IMLA); Aimogasta (La Rioja prov.) (28° 34′ 18 S 66° 48′ 03 W, 847 MASL), 24.XII.07, 3 females, 3 males, 2 nymphs (IMLA), Virla col.; Villa Mazán (La Rioja) (28° 39′ 57.9 S 66° 31′ 24.2 W, 652 MASL), 10.II.08, 24 females, 65 males, 46 nymphs, Virla col. (IMLA); Chumbicha (Catamarca prov.) (28° 48′ 56 S 66° 14′ 50 W, 506 MASL), 21.XII.07, 4 females, 2 males, 3 nymphs, Virla col. (IMLA).

Discussion

Opsius stactogalus was found in all provinces sampled, except Córdoba (National Road n°7 km 526, near Gral. Levalle), in 12 out of the 13 sites surveyed. In all sites O. stactogalus was very abundant, however damage produced by this leafhopper on the sampled plants was not observed. Therefore, the potential usefulness of this hopper as a biocontrol agent for the invasive tamarisk populations established in Argentina is doubtful. Opsius stactogalus was also recorded in the United States of America, and again it did not cause significant damage to Tamarix spp. (De Loach 2001).

These findings encourage exploration for possible natural enemies of O. stactogalus, either natives of Argentina or others that arrived with this leafhopper, in order to better understand the community history of tamarisk in Argentina.

Acknowledgements

The authors would like to thank Miss G. Rios de Fanjul for review of an early draft of the manuscript. We also are grateful to the reviewers for providing valuable suggestions.

Abbreviations

IMLA

Fundación e Institute Miguel Lillo at San Miguel de Tucumán, Argentina;

MLPA

Museo de Ciencias Naturales de La Plata, Buenos Aires;

MASL

meters above sea level

References

  1. Christensen JR. Algunos Cicadelidos de la Argentina y Bolivia. Revista de la Sociedad Entomologica Argentina. 1942;11:336–339. [Google Scholar]
  2. Cordo H, Logarzo G, Braun K, Di Iorio O. Catálogo de los insectos fltófagos de la Argentina y sus plantas asociadas. . 1ra edición. Sociedad Entomológica Argentina ediciones. 2004.
  3. De Loach J. Saltcedar biocontrol: Reconciling risks. CABI Biocontrol News and Information. 2001;22(3) Available online: http://www.pestscience.com/Bni22-3/Gennews.htm. [Google Scholar]
  4. Evans JW. The leafhoppers and froghoppers of Australia and New Zealand. (Homoptera: Cicadelloidea and Cercopoidea). Part 2. Records of the Australian Museum. 1977;31(3):83–129. [Google Scholar]
  5. Fornasari L. Host specificity of Coniatus tamarisci (Coleoptera: Curculionidae) from France: potential biological control agent of Tamarix spp. in the United States. Environmental Entomology. 1997;26:349–356. [Google Scholar]
  6. Fornasari L. Ethology, field biology and host suitability of Coniatus repandus, a natural enemy of tamarisk in France. Bulletin of Insectology. 2004;57(2):117–26. [Google Scholar]
  7. Gaskin JF, Schaal BA. Molecular Phylogenetic Investigation of U.S. invasive Tamarix. Systematic Botany. 2003;28(1):86–95. [Google Scholar]
  8. Harding L. The biology of Opsius stactogalus Fieber (Homoptera: Cicadellidae). Journal of the Kansas Entomological Society. 1930;3:7–22. [Google Scholar]
  9. Jones WA, Logarzo GA, Triapitsyn SV, Casas M, Virla EG, Purcell AH. Proceedings, 12th International Auchenorrhyncha Congress and 6th International Workshop on Leafhoppers and Planthoppers of Economic Significance. University of California; Berkeley, Ca: 2005. Biology and host range of 2 South American egg parasitoids (Hymenoptera: Mymaridae), possible biocontrol agents for Glassy-Winged Sharpshooter, Homalodisca coagulata (Say) (Hemiptera: Cicadellidae; Proconiini). 7–12 August 2005. Available online: http://nature.berkeley.edu/hoppercongress/. [Google Scholar]
  10. León L. Sitios RAMSAR de la Argentina, Laguna de Llancanelo (Provincia de Mendoza). Secretaria de Ambiente y desarrollo sustentable, Ministerio de Salud y Ambiente; Argentina: 2006. Available online: http://www2.medioambiente.gov.ar/recursos_acuaticos/ramsar/llancanelo.htm. [Google Scholar]
  11. Linnavuori R. Revision of the neotropical Deltocephalinae and some related subfamilies (Homoptera). Annales Zoologici Societatis Zoologicae Botanicae Fennicae “Vanamo”. 1959;XX(1):1–370. [Google Scholar]
  12. Linnavuori R, De Long D. The leafhoppers (Homoptera: Cicadellidae) known from Chile. Brenesia. 1977;12/13:163–267. [Google Scholar]
  13. Metcalf ZP. General catalogue of the Homoptera. Fascicle VI, Cicadelloidea. Part 10, Euscelidae. Section I–III. Agricultural Research Service; USDA: 1967. [Google Scholar]
  14. Morrone JJ. Biogeografía de América Latina y el Caribe. Vol. 3. M&T — Manuales & Tesis SEA; 2001. Available online: http://www.sea-entomologia.org/. Accessed 19 March 2008. [Google Scholar]
  15. Natale ES, Gaskin J, Zalba SM, Ceballos M, Reinoso HE. Especies del género Tamarix (Tamaricaceae) invadiendo ambientes naturales y seminaturales en Argentina. Boletín de la Sociedad Argentina de Botánica. 2008;43:137–145. [Google Scholar]
  16. Oman PW. A generic revision of American Bytoscopinae and South American Jassinae. Bulletin of the University of Kansas. 1936;XXXVII(14):343–420. [Google Scholar]
  17. Oman PW, Knight WJ, Nielson MW. Leafhoppers (Cicadellidae): A bibliography, generic check-list and index to the world literature 1956–1985. CAB International Institute of Entomology. 1990:1–287. [Google Scholar]
  18. Sosa H. II Taller de capacitación sobre especies invasoras, en sitio RAMSAR Laguna Llancanelo. Compiled by Heber Sosa; 2003. Informe de resultados. . [Google Scholar]
  19. Wiesenborn W. Inverse densitydependent parasitism of Opsius stactogalus Fieber (Homoptera: Cicadellidae) by Gonatopus sp. (Hymenoptera: Dryinidae). Pan-Pacific Entomologist. 2001;77(2):61–67. [Google Scholar]
  20. Wiesenborn W. Weak dependence of Polynema saga (Girault) (Hymenoptera: Mymaridae) parasitism rate on Opsius stactogalus Fieber (Homoptera: Cicadellidae) egg density. Journal of the Kansas Entomological Society. 2002;75(2):116–22. [Google Scholar]
  21. Zalba SM, Villamil CB. Woody plant invasion in relictual grasslands. Biological Invasions. 2002;4:55–72. [Google Scholar]
  22. Zanol K. Catalogue of the Neotropical (including north of Mexico) Deltocephalinae (Hemiptera-Cicadellidae) Part I. Athysanini and Deltocephalini excluded. Acta Biológica Paranaense. 2006;35(2–4):89–161. [Google Scholar]

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