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1 June 2017 Ceratothripoides brunneus (Thysanoptera: Thripidae) Recorded from Florida
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Abstract

The African thrips Ceratothripoides brunneus Bagnall (Thysanoptera: Thripidae) is reported for the first time from North America, collected from flowers of Asystasia gangetica (L.) T. Anderson (Acanthaceae) in Miami-Dade County, Florida. The affinity of C. brunneus for solanaceous plants in other regions of the world suggests that future detection in Florida commercial tomato, pepper, and eggplant production areas is possible. A literature summary of geographic distribution and biology and a morphological description of adults are provided.

The African thrips Ceratothripoides brunneus Bagnall (Thysanoptera: Thripidae) is widely distributed throughout Sub-Saharan Africa, where it is an important pest of tomatoes, eggplant, peppers, and other Solanaceae (Moritz et al. 2016). Historical specimens from various museum collections examined by Mound & Nickle (2009) suggested that the original range of C. brunneus was confined to the Afrotropical region. However, more recent reports include specimens collected from Puerto Rico (Mound & Nickle 2009), Malaysia (Mound & Azidah 2009), Cuba (Suris & Rodriguez-Romero 2011), Indonesia (Sartiami & Mound 2013), and Guadeloupe (Etienne et al. 2015), indicating that C. brunneus has moved beyond its native range, presumably transported by the horticultural trade (Mound & Azidah 2009). In North America, C. brunneus was intercepted at U.S. ports of entry (Nickle 2003, 2009) but has not been reported outside of quarantine environs. Here we report for the first time the collection of C. brunneus from vegetation in North America.

Little is published about the biology of C. brunneus (Macharia et al. 2015). The species was identified as a likely pollinator of Napoleonaea vogelii Hook. & Planch. (Napoleonaceae) trees in Gabon, Africa (Frame & Durou 2001). Adults of C. brunneus were collected from a variety of plant species, including cultivated crops and weeds (Table 1). Macharia et al. (2015) recorded C. brunneus as the most abundant thrips species in 4 major tomato production areas in Kenya. There are no reports of larvae collected in association with adults on host plants that would demonstrate a host-plant relationship (sensu Mound 2013: a plant on which an insect rears its young), but according to Moritz et al. (2016), C. brunneus breeds mostly on leaves. Identification of host plants not only provides a quantitative measure of a plant's suitability for completion of the insect's life cycle but also indicates the source of the pest population (Terry 1997). Ceratothripodes brunneus is not known to transmit tospoviruses but, given that the congener C. claratris (Shumsher) (Thysanoptera: Thripidae) is a vector of Capsicum chlorosis virus in tomatoes (Premachandra et al. 2005), the potential of C. brunneus as a vector should be investigated in more detail (Macharia et al. 2015).

Table 1.

Plant taxa with collected adults of Ceratothripoides brunneus from published reports.

t01_495.gif

Mound & Nickle (2009) provided a complete morphological diagnosis of the genus Ceratothripoides and the 5 species currently included, all of which previously were confined to the Old World tropics (ThripsWiki 2016). Four Neotropical species originally placed in Ceratothripoides were re-assigned to the genus Retanathrips, based on 3 synapomorphies not shared with the Old World forms. Other morphologically similar genera include Pezothrips, Megalurothrips, Odontothrips, and Odontothripiella (Mound & Nickle 2009).

Females and males of C. brunneus were collected in Miami-Dade County, Florida (25.63955°N, 80.29462°W), from the flowers of Asystasia gangetica (L.) T. Anderson (Acanthaceae) (chinese violet, ganges primrose), an invasive and widely distributed weed in south Florida (Langeland et al. 2008). Specimens were slide prepared, identified using dichotomous keys (Mound & Marullo 1996; Mound & Nickle 2009; Masumoto 2010), and compared with voucher specimens from quarantine inspections of the United States Department of Agriculture- Animal and Plant Health Inspection Service-Plant Protection and Quarantine. Voucher specimens were deposited in the Florida State Collection of Arthropods (FSCA), Gainesville, Florida. An abbreviated morphological description and diagnosis relative to co-occurring species in Florida is provided.

Figs. 1–5.

Ceratothripoides brunneus: 1. female habitus; 2. female forewing scale; 3. female head; 4. male habitus; 5. male abdominal sternites II–VIII.

f01_495.jpg

A combination of characters and states distinguish females of C. brunneus from those of other common flower-inhabiting Thripidae in Florida. Body brown, forewings and scale shaded brown (Fig. 1). Forewing scale with 6–8 marginal setae and discal setae absent (Fig. 2). Antenna 8-segmented. Head with 3 pairs of ocellar setae. Ocellar setae pair I usually arranged longitudinally (Fig. 3). Metanotal campaniform sensilla absent. Abdominal tergal ctenidia absent, but tergite VIII possesses scattered microtrichia sublaterally that may be interpreted as ctenidia. Posteromarginal comb tergite VIII complete and composed of long, evenly spaced microtrichia.

The male, similar in color to the female (Fig. 4), is differentiated from other Thripidae males encountered in Florida by the presence of irregular transverse rows of round to oval pore plates on sternites III– VII (Fig. 5). The pore plates are visible on alcohol preserved specimens under the dissecting microscope.

References Cited

  1. Azidah AA. 2011. Thripidae (Thysanoptera) species collected from common plants and crops in Peninsular Malaysia. Scientific Research and Essays 6: 5107–5113. Google Scholar

  2. Etienne J, Ryckewaert P, Michel B. 2015. Thrips (Insecta: Thysanoptera) of Guadeloupe and Martinique: updated check-list with new information on their ecology and natural enemies. Florida Entomologist 98: 298–304. Google Scholar

  3. Frame D, Durou S. 2001. Morphology and biology of Napoleonaea vogelii (Lecythidaceae) flowers in relation to the natural history of insect visitors. Biotropica 33: 458–471. Google Scholar

  4. Langeland KA, Cherry HM, McCormick CM, Craddock Burk KA. 2008. Identification and biology of non-native plants in Florida's natural areas. Publication SP 257. University of Florida, Institute of Food and Agricultural Sciences, Gainesville, Florida. Google Scholar

  5. Macharia I, Backhouse D, Skilton R, Ateka E, Wu SB, Njahira M, Maina S, Harvey J. 2015. Diversity of thrips species and vectors of Tomato spotted wilt virus in tomato production systems in Kenya. Journal of Economic Entomology 108: 20–28. Google Scholar

  6. Masumoto M. 2010. Key to genera of the subfamily Thripinae (Thysanoptera: Thripidae) associated with Japanese plant quarantine. Research Bulletin of the Plant Protection Service Japan 46: 25–59. Google Scholar

  7. Moritz G, Brandt S, Triapitsyn S, Subramanian S. 2016. Identification and information tools for thrips in East Africa,  http://thripsnet.zoologie.uni-halle.de/key-server-neu/data/03030c05-030b-4107-880b-0a0a0702060d/media/Html/index.html (last accessed 23 Nov 2016). Google Scholar

  8. Mound LA. 2013. Homologies and host-plant specificity: recurrent problems in the study of thrips. Florida Entomologist 96: 318–322. Google Scholar

  9. Mound LA, Azidah AA. 2009. Species of the genus Thrips (Thysanoptera) from peninsular Malaysia, with a checklist of recorded Thripidae. Zootaxa 2023: 55–68. Google Scholar

  10. Mound LA, Marullo R. 1996. The thrips of Central and South America: an introduction (Insecta: Thysanoptera). Memoirs on Entomology, International 6: 1–487. Google Scholar

  11. Mound LA, Nickle DA 2009. The Old-World genus Ceratothripoides (Thysanoptera: Thripidae) with a new genus for related New-World species. Zootaxa 2230: 57–63. Google Scholar

  12. Nickle DA. 2003. A checklist of commonly intercepted thrips (Thysanoptera) from Europe, the Mediterranean, and Africa at U.S. ports-of-entry (1983– 1999). Part I. Key to genera. Proceedings of the Entomological Society of Washington 105: 80–99. Google Scholar

  13. Nickle DA. 2009. Commonly intercepted thrips at U.S. ports-of-entry from Africa, Europe, and the Mediterranean. IV. Miscellaneous thripine genera excluding Frankliniella, Iridothrips, and Thrips (Thysanoptera, Thripidae). Proceedings of the Entomological Society of Washington 111: 215–238. Google Scholar

  14. Premachandra WT, Borgemeister C, Maiss E, Knierim D, Poehling HM. 2005. Ceratothripoides claratris, a new vector of a Capsicum chlorosis virus isolate infecting tomato in Thailand. Phytopathology 95: 659–663. Google Scholar

  15. Sartiami D, Mound LA. 2013. Identification of the terebrantian thrips (Insecta, Thysanoptera) associated with cultivated plants in Java, Indonesia. ZooKeys 306: 1–21. Google Scholar

  16. Suris M, Rodriguez-Romero A. 2011. Correction of Ceratothripoides claratris reports to Ceratothripoides brunneus (Thysanoptera: Thripidae) in Cuba. Revista de Protección Vegetal 26: 134. Google Scholar

  17. Terry I. 1997. Host selection, communication and reproductive behavior, pp. 65–118 In Lewis T [ed.], Thrips as Crop Pests. CAB International, Oxfordshire, United Kingdom. Google Scholar

  18. ThripsWiki. 2016. ThripsWiki contributors,  http://thrips.info/wiki/Ceratothripoides (last accessed 7 Nov 2016). Google Scholar

Thomas Skarlinsky, Joe Funderburk, and Felipe Soto-Adames "Ceratothripoides brunneus (Thysanoptera: Thripidae) Recorded from Florida," Florida Entomologist 100(2), (1 June 2017). https://doi.org/10.1653/024.100.0245
Published: 1 June 2017
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