Diorhabda carinata

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Diorhabda carinata
DiorhabdacarinataAshgTurkm.jpg
Scientific classification
Kingdom:
Animalia
Phylum:
Arthropoda
Class:
Insecta
Order:
Coleoptera
Family:
Chrysomelidae
Subfamily:
Galerucinae
Genus:
Diorhabda
Species:
D. carinata
Binomial name
Diorhabda carinata
(Faldermann, 1837)  [1]
Synonyms
  • Galeruca carinataFaldermann, 1837
  • Diorhabda elongata carinata(Faldermann, 1837)

Diorhabda carinata is a species of leaf beetle known as the larger tamarisk beetle (larger tamarisk beetle) which feeds on tamarisk trees from Ukraine, eastern Turkey and Syria east to northwest China, Kyrgyzstan and Pakistan, extending as far south as southern Iran. [Note 1] It is used in North America as a biological pest control agent against saltcedar or tamarisk ( Tamarix spp.), an invasive species in arid and semi-arid ecosystems (where the larger tamarisk beetle and its closely related sibling species also may be less accurately referred to as the 'saltcedar beetle', 'saltcedar leaf beetle', 'salt cedar leaf beetle', or 'tamarisk leaf beetle'). [2]

Contents

Taxonomy

The larger tamarisk beetle was first described from the Transcaucasus (Georgia and Azerbaijan) as Galeruca carinata Faldermann, 1837. [1] Reiche and Saulcy placed G. carinata as a junior synonym to the sibling species G. elongata Brullé (the Mediterranean tamarisk beetle, Diorhabda elongata ). [3] Weise created the genus Diorhabda in 1893 and proposed the color variant Diorhaba elongata var. carinata (Faldermann), [4] and he also placed the sibling species Galeruca carinulata Desbrochers (the northern tamarisk beetle, Diorhabda carinulata ) as a junior synonym of this variant. Jan Bechyné (1961) proposed the subspecies D. e. carinata listing specimens from Afghanistan. [5] Berti and Rapilly (1973) recognized D. carinata and D. carinulata as separate species from one another, and, by implication, as separate species from D. elongata, based on detailed morphology of the endophallus of the male genitalia. [6] Tracy and Robbins (2009) [2] confirmed the 1973 findings of Berti and Rapilly, [6] further characterized the male and female genitalia of D. carinata, and provided illustrated taxonomic keys separating the larger tamarisk beetle from the four other sibling species of the D. elongata (Brullé) species group: Diorhabda elongata , Diorhabda sublineata (Lucas), Diorhabda carinulata , and Diorhabda meridionalis Berti and Rapilly. In literature prior to 2009, D. carinata was usually also referred to as D. elongata, or subspecies of D. elongata.

Host plants

Field collections in Eurasia reveal that the larger tamarisk beetle feeds on at least nine species of tamarisks, including Tamarix ramosissima which is widely invasive in western North America. The larger tamarisk beetle will severely defoliate tamarisk in Turkmenistan and Tajikistan. [2] Extensive laboratory host range studies verified that larger tamarisk beetle is a specialist feeder on tamarisks, feeding only on plants of the tamarisk family, Tamaricaceae. In laboratory and field cage studies, the larger tamarisk beetle will also feed and complete development on Frankenia shrubs, distant relatives of tamarisks in the same plant order Caryophyllales, but larger tamarisk beetle greatly prefer to lay eggs upon tamarisk. [7]

Life cycle

The larger tamarisk beetle overwinters as adults on the ground. Adults become active and begin feeding and mating in the early spring when tamarisk leaves are budding. Eggs are laid on tamarisk leaves and bark and hatch in about a week in warm weather. Three larval stages feed on tamarisk leaves for about two and a half weeks when they crawl to the ground and spend about 5 days as a C-shaped inactive prepupa before pupating about one week. Adults emerge from pupae to complete the life cycle in about 4–5 weeks in the summer. Five generations of larger tamarisk beetle occur through spring and fall in central Texas. [8] Similar to the northern tamarisk beetle, adults begin to enter diapause in the late summer and early fall, ceasing reproduction and feeding to build fat bodies before seeking a protected place to overwinter. [9] Larvae and adults are sensitive to shorter daylengths as the summer progresses that signal the coming of winter and induce diapause. [10] Robert Bartelt and Allard Cossé (USDA-ARS, Peoria, Illinois) found that male larger tamarisk beetle emit a putative aggregation pheromone, similar to that found in Diorhabda carinulata, [11] that could serve to attract both males and females to certain tamarisk trees.

Biological control agent

The larger tamarisk beetle is currently weakly established as a biological control agent for tamarisk in west Texas. Populations of larger tamarisk beetle from around 39°N latitude near Qarshi, Uzbekistan were initially released by the USDA Agricultural Research Service in west Texas in 2006. By 2008, the larger tamarisk beetle had defoliated about 0.2 hectares of tamarisk near Seymour, Texas. The larger tamarisk beetle may be better adapted to warm temperate grassland and desert habitats of west Texas than other Old World tamarisk beetles that are being introduced, such as the Mediterranean tamarisk beetle, Diorhabda elongata . The northern tamarisk beetle, Diorhabda carinulata , is probably better adapted to northern cold deserts in North America where it is widely established, and the subtropical tamarisk beetle, Diorhabda sublineata , may be better adapted to subtropical deserts. [2]

Tamarisk does not usually die from a single defoliation from tamarisk beetles, and it can resprout within several weeks of defoliation. Repeated defoliation of individual tamarisk trees can lead to severe dieback the next season and death of the tree within several years. [12] Tamarisk beetle defoliation over the course of at least one to several years can severely reduce the nonstructural carbohydrate reserves in the root crowns of tamarisk. [13] Biological control of tamarisk by the larger tamarisk beetle will not eradicate tamarisk but it has the potential to suppress tamarisk populations by 75–85%, after which both larger tamarisk beetle and tamarisk populations should reach equilibrium at lower levels. [12] [14]

A primary objective of tamarisk biological control with the larger tamarisk beetle is to reduce competition by exotic tamarisk with a variety of native riparian flora, including trees (willows, cottonwoods, and honey mesquite), shrubs (wolfberry, saltbush, and baccharis), and grasses (alkali sacaton, saltgrass, and vinemesquite). Unlike expensive chemical and mechanical controls of tamarisk that often must be repeated, tamarisk biological control does not harm native flora and is self-sustaining in the environment. Recovery of native riparian grasses can be quite rapid under the once closed canopy of repeatedly defoliated tamarisk. However, tamarisk beetle defoliation can locally reduce nesting habitat for riparian woodland birds until native woodland flora are able to return. In some areas, tamarisk may be replaced by grasslands or shrublands, resulting in losses of riparian forest habitats for birds (Tracy and DeLoach 1999). Releases of tamarisk beetles in southern California, Arizona, and along the Rio Grande in western New Mexico, are currently delayed until concerns can be resolved regarding safety of tamarisk biological control to nesting habitats of the federally endangered southwestern willow flycatcher, Empidonax traillii Audubon subspecies extimus Phillips, which will nest in tamarisk. [15]

Notes

  1. ↑ Tracy and Robbins (2009) [2] provide a detailed review of the distribution, biogeography, biology, and taxonomy of D. carinata.

Related Research Articles

Willow flycatcher

The willow flycatcher is a small insect-eating, neotropical migrant bird of the tyrant flycatcher family. There are four subspecies of the willow flycatcher currently recognized, all of which breed in North America. Empidonax flycatchers are almost impossible to tell apart in the field so biologists use their songs to distinguish between them. The binomial commemorates the Scottish zoologist Thomas Stewart Traill.

<i>Tamarix</i> Genus of plants

The genus Tamarix is composed of about 50–60 species of flowering plants in the family Tamaricaceae, native to drier areas of Eurasia and Africa. The generic name originated in Latin and may refer to the Tamaris River in Hispania Tarraconensis (Spain).

<i>Aphthona</i> Genus of beetles

Aphthona is a genus of beetle, in the leaf beetle family Chrysomelidae, native to Europe and Asia. More specifically, Aphthona are flea beetles, meaning they have enlarged hind legs for jumping away from potential danger. There are 135 species known from the Palaearctic region.

<i>Ulmus changii</i>

Ulmus changiiW. C. Cheng, occasionally known as the Hangzhou elm, is a small deciduous tree found across much of China in forests at elevations of up to 1800 m. Owing to its increasing scarcity, U. changii was added to the Hainan Province Protected Plants List in 2006.

The American Elm cultivar Ulmus americana 'Littleford' was cloned from a tree in Hinsdale, Illinois, circa 1915 and first released in 1927.

Aphthona czwalinae is a species of leaf beetle known as the black leafy spurge flea beetle. It is used as an agent of biological pest control against the noxious weed leafy spurge.

<i>Cassida</i> Genus of beetles

Cassida is a large Old World genus of tortoise beetles in the subfamily Cassidinae. Several species of Cassida are important agricultural pests, in particular C. vittata and C. nebulosa on sugar beet and spinach. The thistle tortoise beetle has been used as a biological control agent against Canada thistle.

<i>Northern tamarisk beetle</i> Species of beetle

Diorhabda carinulata is a species of leaf beetle known as the northern tamarisk beetle, which feeds on tamarisk trees from southern Russia and Iran to Mongolia and western China. This beetle is used in North America as a biological pest control agent against saltcedar or tamarisk, an invasive species in arid and semiarid ecosystems.

<i>Diorhabda elongata</i> Species of beetle

Diorhabda elongata is a species of leaf beetle known as the Mediterranean tamarisk beetle (MTB) which feeds on tamarisk trees from Portugal and Algeria east to southern Russia. The MTB is used in North America as a biological pest control agent against saltcedar or tamarisk, an invasive species in arid and semi-arid ecosystems.

<i>Diorhabda sublineata</i> Species of beetle

Diorhabda sublineata is a leaf beetle known as the subtropical tamarisk beetle (STB). The species was first described by Hippolyte Lucas in 1849. It feeds on tamarisk trees from Portugal, Spain and France to Morocco, Senegal, Algeria, Tunisia, Egypt, Yemen, and Iraq. It is used in North America as a biological pest control agent against saltcedar or tamarisk, an invasive species in arid and semi-arid ecosystems.

<i>Diorhabda meridionalis</i> Species of beetle

Diorhabda meridionalis is a species of leaf beetle known as the southern tamarisk beetle (SoTB) which feeds on tamarisk trees from Syria to western and southern Iran and southern Pakistan. The SoTB may have potential for use in North America as a biological pest control agent against saltcedar or tamarisk, an invasive species in arid and semi-arid ecosystems.

Aphthona lacertosa is a root-feeding flea beetle of the genus Aphthona. It is one of 5 Aphthona spp. that has been used in Alberta, Canada to control leafy spurge, an invasive plant that reduces pasture quality and degrades natural habitats.

<i>Gratiana boliviana</i> Species of beetle

Gratiana boliviana is a species of beetle in the leaf beetle family, Chrysomelidae. Its common name is tropical soda apple leaf beetle. It is native to South America, where its distribution includes Argentina, Brazil, and Paraguay. It specializes on tropical soda apple, an invasive plant species. It has been released as an agent of biological pest control against the weedy plant in Florida and other parts of the United States.

Chloropterus politus is a species of leaf beetle from Iran and Oman. It was first described from Minab by Berti & Rapilly in 1973.

<i>Zygogramma suturalis</i> Species of beetle

Zygogramma suturalis, commonly known as the ragweed leaf beetle, is a species of leaf beetle belonging to the genus Zygogramma. Native to North America, it has been introduced into Russia and China for the biological pest control of ragweed.

<i>Paropsis charybdis</i> Species of beetle

Paropsis charybdis, commonly known as the Eucalyptus tortoise beetle, is a species of leaf beetle belonging to the genus Paropsis. It is consider a pest of some species of Eucalyptus.

Cleorina is a genus of leaf beetles in the subfamily Eumolpinae. It is known from Australia and Asia.

Stethotes is a genus of leaf beetles in the subfamily Eumolpinae.

Aulexis is a genus of leaf beetles in the subfamily Eumolpinae. It is distributed in East and Southeast Asia. The related genus Goniopleura is sometimes included as a subgenus.

<i>Trachymela sloanei</i> Species of beetle

Trachymela sloanei, known generally as the Australian tortoise beetle or small eucalyptus tortoise beetle, is a species of leaf beetle in the family Chrysomelidae.

References

  1. 1 2 Faldermann, F. 1837: Fauna entomologica Trans-Caucasica, II: Coleoptera. Nouveaux Mémoires de la Société Impériale des Naturalistes de Moscou, 5: 1–433. (In Latin)
  2. 1 2 3 4 Tracy, J. L.; Robbins, T. O. 2009: Taxonomic revision and biogeography of the Tamarix-feeding Diorhabda elongata (Brullé, 1832) species group (Coleoptera: Chrysomelidae: Galerucinae: Galerucini) and analysis of their potential in biological control of Tamarisk. Zootaxa , 2101: 1-152. (PDF)
  3. ↑ Reiche, L.; Saulcy, F. 1858: Espèces nouvelles ou peu connues de Colèoptères, recueillies par M.F. de Saulcy, member de l’Institute, dans son voyage en Orient, et dècrites par M. M. L. Reiche et Fèlicien de Saulcy. Annales de la Société Entomologique de France, Sér., 3, 6: 5–60. (In French)
  4. ↑ Weise, J. 1893: Chrysomelidae. In: W. Erichson (ed.), Naturgeschichte der Insecten Deutschland, 61 (73): 961–1161. (In German)
  5. ↑ Bechyné, J. 1961: Ergebnisse der Deutschen Afghanistan–Expedition 1956: Chrysomelidae, Galerucidae und Alticidae. Beiträge zur Naturkunde Forschung Südwestdeutschland, Karlsruhe, 19 (3): 255–257. (In German)
  6. 1 2 Berti, N.; Rapilly, M. 1973: Contribution a la faune de l’Iran; Voyages de MM. R. Naviaux et M. Rapilly (Col. Chrysomelidae). Annales de la Société Entomologique de France , 9 (4): 861–894. (In French)
  7. ↑ Milbrath, L.; DeLoach, C. J. 2006: Host specificity of different populations of the leaf beetle Diorhabda elongata (Coleoptera: Chrysomelidae), a biological control agent of saltcedar (Tamarix spp.). Biological Control , 36: 32–48. (PDF)
  8. ↑ Milbrath, L.; DeLoach, C. J.; Tracy, J. L; 2007: Overwintering survival, phenology, voltinism, and reproduction among different populations of the leaf beetle Diorhabda elongata (Coleoptera: Chrysomelidae). Environmental Entomology , 36 (6): 1356–1364. (PDF)
  9. ↑ Lewis, P. A.; DeLoach, C. J.; Knutson, A. E.; Tracy, J. L.; Robbins, T. O. 2003: Biology of Diorhabda elongata deserticola (Coleoptera: Chrysomelidae), an Asian leaf beetle for biological control of saltcedars (Tamarix spp.) in the United States. [ permanent dead link ] Biological Control , 27: 101–116. (PDF)
  10. ↑ Bean, D. W.; Keller, J. C. in prep.: Characteristics of diapause induction in populations of Diorhabda elongata collected from sites in Europe, Africa and Asia: Implications for tamarisk (Tamarix spp) biocontrol in North America. For publication in Biological Control .
  11. ↑ Cossé, A. A.; Bartelt, R. J.; Zilkowski, B. W.; Bean, D. W.; Petroski, R. J. 2005: The aggregation pheromone of Diorhabda elongata, a biological control agent of saltcedar (Tamarix sp.): identification of two behaviorally active components. Journal of Chemical Ecology , 31 (3): 657–670. (PDF)
  12. 1 2 DeLoach, C. J.; Carruthers, R. 2004: Biological control programs for integrated invasive plant management. In: Proceedings of Weed Science Society of America Meeting, Kansas City, MO. Weed Science Society of America (CD-ROM). 17 pp. (PDF)
  13. ↑ Hudgeons, J. L.; Knutson, A. E.; Heinz, K. M.; DeLoach, C. J.; Dudley, T. L.; Pattison, R. R.; Kiniry, J. R. 2007: Defoliation by introduced Diorhabda elongata leaf beetles (Coleoptera: Chrysomelidae) reduces carbohydrate reserves and regrowth of Tamarix (Tamaricaceae). Biological Control , 43: 213–221. (PDF)
  14. ↑ Tracy, J. L.; DeLoach, C. J. 1999: Biological control of saltcedar in the United States: Progress and projected ecological effect. Archived 2011-07-23 at the Wayback Machine In: C. E. Bell (ed.), Arundo and Saltcedar: The Deadly Duo, Proceedings of the Arundo and Saltcedar Workshop, 17 June 1998. Ontario, California, 111–154. (PDF)
  15. ↑ Dudley, T. L. DeLoach, C. J. 2004: Saltcedar (Tamarix spp.), endangered species, and biological weed control-can they mix? Weed Technology , 18 (5): 1542–1551. (PDF)
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