Translator Disclaimer
1 September 2016 Host Specificity Evaluation for Gynaikothrips uzeli (Thysanoptera: Phlaeothripidae) on Ornamental Ficus (Rosales: Moraceae)
Author Affiliations +

The weeping fig thrips Gynaikothrips uzeli Zimmerman (Thysanoptera: Phlaeothripidae) is an invasive pest that is being spread via shipments of ornamental Ficus (Rosales: Moraceae). We tested 50 Ficus cultivars from 12 species for their suitability as hosts for G. uzeli under greenhouse conditions. Results showed that G. uzeli reproduced well only on F. benjamina L.; other species were much less suitable. Plants of F. benjamina sustained folded leaf galls in new growth within 2 to 3 d of being exposed to adult thrips. In subsequent tests, we noted some differences among 27 F. benjamina cultivars in terms of the degree of infestation (number of leaves galled) and reproductive output of G. uzeli over 1 to 2 generations. Plant variegation did neither affect the number of galled leaves nor the number of thrips recovered in our studies. Our results suggest that genetic variation exists among F. benjamina cultivars in resistance to G. uzeli infestation. Additionally, Ficus species other than F. benjamina may be substituted in cases where G. uzeli is potentially troublesome.

Gynaikothrips (Thysanoptera: Phlaeothripidae) comprises approximately 40 species of dark brown to black thrips that originate in Southeast Asia and that induce galls on developing leaf tissues of Ficus species (Rosales: Moraceae) (Dang et al. 2014). These galls cause aesthetic impacts to ornamental Ficus, although they are otherwise not harmful, and provide habitat for other arthropods (inquilines), including natural enemies of Gynaikothrips (Mound & Morris 2005; Tree & Walter 2009). In recent years, Gynaikothrips species have colonized Asia, Africa, and Central America, probably through international trade in Ficus plants. For example, the weeping fig thrips G. uzeli Zimmerman was discovered in the United States in Florida in 2003 and spread rapidly throughout the southeastern states via shipments of ornamental weeping fig (F. benjamina L.) originating from nurseries in southern Florida (Held et al. 2005). This pest has since been reported from at least 10 states in the contiguous United States, as well as Hawaii and Puerto Rico (Cabrera-Asencio et al. 2008; Held & Boyd 2008a; Dara & Hodel 2015), and from Brazil (Cavalleri et al. 2011), Australia (Tree 2012), India (Tyagi 2012), Panama (Goldarazena et al. 2012), and Syria (Ali 2014).

Weeping fig thrips is very similar to the earlier-described Cuban laurel thrips, G. ficorum Marchal, which has been known from the continental United States since at least 1887 (Denmark 1967). The only known difference between G. uzeli and G. ficorum is the length of the pronotal setae (Mound et al. 1995). However, these species are associated with different hosts. Whereas G. uzeli is known to infest F. benjamina, G. ficorum is primarily associated with Chinese Banyan, F. microcarpa L.f., and has established a pantropical distribution wherever this plant occurs (Mound et al. 1995; ThripsWiki 2015).

Although host plant is thought to be a good indicator to differentiate G. uzeli and G. ficorum, identification of Ficus species by entomologists may not be entirely reliable. A recent study reported that G. ficorum was able to produce leaf galls on both F. benjamina and F. microcarpa under greenhouse conditions, whereas G. uzeli was able to induce galls only on F. benjamina (Tree et al. 2015). However, the ability of G. uzeli to feed upon or reproduce on other Ficus species is unclear. Furthermore, preferences of G. uzeli among cultivars of F. benjamina have not been reported. We therefore conducted host specificity tests of G. uzeli among various Ficus species and on various cultivars of F. benjamina.

Materials and Methods


All experiments were conducted in research greenhouses at the Mid-Florida Research and Education Center, Apopka, Florida. Fifty cultivars of Ficus from 12 species were collected and maintained in a germplasm conservation greenhouse (Fang et al. 2007) and propagated through stem cutting. Propagated plants were grown as stocks in pots (11.4 L) with a sphagnum peat-sand based substrate and fertilized periodically with 10 g of controlled-release granules (15-9-12 Osmocote Plus, the Scotts Co., Marysville, Ohio) per pot. Thrips (G. uzeli) were collected from natural infestations on F. benjamina ‘Midnight' and used to start a colony that was cultured in a separate greenhouse on the same cultivar.


The 50 cultivars were tested in the 1st experiment for their suitability as hosts for G. uzeli under greenhouse conditions. Cuttings were made from stock plants, and rooted cuttings were transplanted into 10 cm diameter pots fertilized with 15-7-15 (Multicote 8 at 3 g per pot + 1.2 mg minors). Plants were approximately 6 mo old (post transplanting) and 30 cm tall when used. Plants were placed individually in cages, and each cage also had F. benjamina ‘Midnight' as a known positive (susceptible) control. There were 3 replicates per cultivar. Cages were maintained under greenhouse conditions. Five adults thrips removed from the colony were placed in each cage. Cages were examined after 3 d and again after 60 d, when approximately 2 generations of thrips may have occurred. All cultivars with leaf galls containing reproducing populations of G. uzeli were noted.


Because F. benjamina was clearly the most susceptible species to G. uzeli, we conducted 2 further choice tests to more thoroughly evaluate various cultivars of F. benjamina to determine their relative susceptibility to this insect under greenhouse conditions. Some cultivars were variegated with yellow or pale green coloration. Rooted cuttings were transplanted as before, when new growth suitable for galling behavior of G. uzeli was available.

A choice study was conducted to evaluate feeding preferences among 23 cultivars. Four plants of each cultivar in 15 cm diameter pots were similarly pruned and placed in a randomized block design inside a greenhouse bay in late summer (Aug). Two hundred G. uzeli adults were added to the center of the greenhouse bay on 3 occasions (after 22, 29, and 36 d) when new growth was appearing on plants. Plants were about 40 cm tall at this time. The number of thrips-galled leaves was counted from test plants on 3 subsequent occasions (days 52, 69, and 92 after the initial infestation). The numbers of thrips were evaluated at the end of the study by collecting plant terminals and extracting thrips in the laboratory in 70% ethanol and counting life stages under a binocular microscope.

A 2nd study was conducted the following year to evaluate feeding preferences among 27 cultivars. Young plants (2 mo old in 10 cm diameter pots) were pruned to 15 cm prior to tests and used when approximately 3 new leaves were available. A single plant of each variety was placed in a random order in a nylon mesh cage (60 × 60 × 60 cm), and 100 adults of G. uzeli were added in a vial in the center of the cage and allowed to distribute naturally (Fig. 1). The study was conducted (replicated) on 3 separate occasions, based on the availability of plants. In each case, the number of leaf galls per plant was counted at 2, 4, and 6 wk after infestation. Thrips were counted at the final assessment by placing galled leaves in 70% ethanol and by extracting thrips in the laboratory.


Plant injury (galled leaves) and the number of thrips recovered in the tests were compared among all cultivars with 1-way ANOVA, with means separated via Tukey's HSD test following a log(n + 1) transformation to control for data normality. The same response variables were similarly compared between cultivars that exhibited variegation and those that did not.



Gynaikothrips uzeli was recovered from all 27 cultivars of F. benjamina in these tests, but was not generally recovered from other Ficus species (Table 1). The first leaf galls were observed with 3 d of introduction of thrips. Of the 454 leaf galls counted at day 60, we noted only a single leaf gall on an F. carica L. and F. neriifolia Smith plant, but we did not confirm that thrips were able to complete their reproduction on these species.


In the 1st study, leaf galls were observed on 22 of the 23 F. benjamina cultivars tested; only the variegated ‘Dwarf Nina' did not become infested in this test. The proportion of galled leaves increased over time, reaching more than 30 leaves per plant for some varieties and with >1,000 thrips recovered (Table 2). Overall, the majority (about 60%) of recovered thrips were larvae. The infestation degree (at the end of the study) varied among cultivars in terms of both the number of galled leaves (F22,69 = 10.5; P < 0.001) and the number of thrips recovered (F22,69 = 8.8; P < 0.001). Plant variegation did not affect the number of galled leaves (F1,90 = 1.4; P = 0.25) or the number of thrips recovered (F1,90 = 1.6; P = 0.21)

In the 2nd study, leaf galls were recovered from 26 of the 27 varieties of F. benjamina; only ‘Midnight Princess' did not become infested (Table 3). However, compared with the previous study, the number of leaf galls was relatively low (average of 1.4 per plant at week 6) and neither the overall injury level at the end of the study (F26,54 = 0.58; P = 0.94) nor the total number of thrips recovered from plant extractions at week 6 (F26,54 = 0.6; P = 0.92) varied among cultivars. Plant variegation affected neither the number of galled leaves (F1,79 = 0.12; P = 0.70) nor the number of thrips recovered (F1,79 = 0.24, P = 0.63).


There is little information concerning host preference of G. uzeli on Ficus species. Our studies documented the apparent host specificity of G. uzeli for F. benjamina when exposed to young plants under greenhouse conditions in central Florida. As reported earlier (Tree et al. 2015), we found that G. uzeli was unable to reproduce on F. microcarpa; however, we extended this observation to several other Ficus species. Although it appeared that adult thrips can feed sporadically on other Ficus species, they did not induce galling or lay eggs. There is a report of G. uzeli infesting tomato in India, although no reproduction was observed (Chavan et al. 2014).

Fig 1.

Cage setup for Ficus benjamina variety choice test with Gynaikothrips uzeli in the greenhouse (year 2).


We also documented some differences among cultivars of F. benjamina. In general, all cultivars appeared to be susceptible; however, we noted differences in the 2nd study, with some varieties such as ‘Profit Compacta' and ‘Dwarf Nina' having fewer thrips than others. A possible explanation is that genetic variation in resistance to G. uzeli infestation exists among cultivated F. benjamina (Fang et al. 2007), particularly for those adapted to Florida environmental conditions, such as ‘Dwarf Nina', ‘Pandora', ‘Profit Compacta', and ‘Silver Cloud'. The use of more pest resistant cultivars in production may reduce economic loss in Ficus production. Differences also may have reflected host plant growth, because the generation of new leaves available for galling was not always consistent among species or cultivars. We noted lower overall density of thrips in the final study, which may have affected their dispersal and host selection behavior.

Our studies confirmed the inability of G. uzeli to initiate galls in fully expanded leaves; only leaves under differentiation could be induced to gall. We noted that adult thrips selected young expanding leaves, apparently causing rapid cell differentiation on the upper surface, and causing the leaf to fold along the mid-vein and purplish spots to develop inside the gall within 2 to 3 d. Females deposited white cylindrical eggs in batches of 100 or more, and a generation of thrips developed inside each gall over approximately 4 wk. We observed that the galls were relatively persistent and did not immediately fall off plants once the new generation of thrips had departed. Galls made by G. uzeli can be inhabited by inquilines, including other members of the Phlaeothripidae, as well as mealybugs, scales, whiteflies, and various natural enemies (Mound et al. 1995; Held et al. 2005).

Ficus benjamina and F. microcarpa are among the most widely cultivated ornamental figs (Fang et al. 2007). The ‘leaf-fold' galls made by G. uzeli in F. benjamina contrast the ‘leaf-roll' galls made by G. ficorum in F. microcarpa (Mound et al. 1995). However, the ability of G. ficorum to induce leaf galls on F. benjamina (Tree et al. 2015) suggests the possibility for inter-specific competition in areas where both thrips species are sympatric. The fact that G. ficorum is rarely reported from F. benjamina in the field suggests that G. uzeli might be a superior competitor on this host, although this remains to be confirmed experimentally.

Due to its cryptic habitat, control of G. uzeli with contact insecticides is not effective (Held & Boyd 2008b). In established landscapes, natural enemies can prevent large outbreaks of this pest. In southern Florida, the predatory pirate bug Montandoniola confusa Streito and Matocq (Hemiptera: Anthocoridae) is an effective predator (Arthurs et al. 2011). Desiccated (fed upon) eggs inside old leaf galls are the most common sign of M. confusa activity in the landscape (authors' personal observations). Other natural enemies of G. uzeli include the predatory thrips Liothrips takahashii Moulton (Tree et al. 2015) and Androthrips ramachandrai Karny (de Melo et al. 2013) (Thysanoptera: Phlaeo thripidae), as well as generalist predators including green lacewings and spiders, and at least 2 eulophid parasitoid species that specialize on phlaeothripine thrips (LaSalle 1994; Held et al. 2005). Preserving the activity of these natural enemies will help reduce the need for insecticides.

Table 1.

Species and cultivars of Ficus in which leaf galls initiated by Gynaikothrips uzeli were recovered (+) at 3 and 60 d post infestation under greenhouse conditions.


In conclusion, this study provides new information on the host selection of G. uzeli. It appears that this species can complete its life cycle only on F. benjamina, not on other Ficus species. Among the 27 F. benjamina cultivars tested, variation existed in response to G. uzeli infestation. The recent (2014) detection of this pest in Los Angeles County, California (Dara & Hodell 2015) confirms that this invasive species is still spreading and that further efforts to improve its detection and management are warranted.

Table 2.

Mean numbers of curled leaves observed at 3 points in time and numbers of adult and larval Gynaikothrips uzeli thrips at the end of the study for 23 Ficus benjamina cultivars (year 1).


Table 3.

Mean numbers of curled leaves observed at 3 points in time and numbers of Gynaikothrips uzeli life stages at the end of the study for 27 Ficus benjamina cultivars in greenhouse cages (year 2).



We are grateful to Robert Leckel, Rosie Fowler, and Mary Brennan for help with the experiments.

References Cited


Ali AY. 2014. Gynaikothrips uzeli (Thysanoptera: Phlaeothripidae), new record from Tartous, Syria. Journal of Insect Science 14: 273. Google Scholar


Arthurs S, Chen J, Dogramaci M, Ali AD, Mannion C. 2011. Evaluation of Montandoniola confusa Streito and Matocq sp. nov. and Orius insidiosus Say (Heteroptera: Anthocoridae), for control of Gynaikothrips uzeli Zimmerman (Thysanoptera: Phlaeothripidae) on Ficus benjamina. Biological Control 57: 202–207. Google Scholar


Cabrera-Asencio I, Ramirez A, Saez L, Velez AL. 2008. Gynaikothrips uzeli Zimmerman (Thysanoptera: Phlaeothripidae) y Montandoniola moraguezi Puton (Hemiptera: Anthocoridae): neuvos records para Puerto Rico. Journal of Agriculture of the University of Puerto Rico 92: 111–113. Google Scholar


Cavalleri A, Lima MGA, Melo FS, Mendonça Jr MS. 2011. New records of thrips (Thysanoptera) species in Brazil. Neotropical Entomology 40: 628–630. Google Scholar


Chavan VM, Chandrashekar K, Bhosle AB. 2014. Occasional occurrence of Gynaikothrips uzeli Zimmerman on tomato. Current Biotica 8: 86–88. Google Scholar


Dang LH, Mound LA, Qiao GX. 2014. Conspectus of the Phlaeothripinae genera from China and Southeast Asia (Thysanoptera, Phlaeothripidae). Zootaxa 3807: 1–82. Google Scholar


Dara SK, Hodel DR. 2015. Weeping fig thrips (Thysanoptera: Phlaeothripidae) in California and a review of its biology and management options. Journal of Integrated Pest Management 6: 4 pp. Google Scholar


de Melo FS, Cavalleri A, de Souza Mendonca Jr M. 2013. Predation of Gynaikothrips uzeli (Thysanoptera: Phlaeothripidae) by Androthrips ramachandrai (Thysanoptera: Phlaeothripidae). Florida Entomologist 96: 859–863. Google Scholar


Denmark HA. 1967. Cuban laurel thrips, Gynaikothrips ficorum, in Florida. Florida Department of Agriculture Entomological Circular 59: 1–2. Google Scholar


Fang J, Chen J, Henny RJ, Chao CCT. 2007. Genetic relatedness of ornamental Ficus species and cultivars analyzed by amplified fragment length polymorphism markers. Journal of the American Society for Horticultural Science 132: 807–815. Google Scholar


Goldarazena A, Gattesco F, Atencio R, Korytowski C. 2012. An updated checklist of the Thysanoptera of Panama with comments on host associations. Check List 8: 1232–1247. Google Scholar


Held DW, Boyd DW. 2008a. New records of Gynaikothrips uzeli (Zimmerman) (Thysanoptera: Phlaeothripidae) on Ficus benjamina in Texas and O'ahu, Hawaii, USA. Pan-Pacific Entomologist 84: 77–80. Google Scholar


Held DW, Boyd D. 2008b. Evaluation of sticky traps and insecticides to prevent gall induction by Gynaikothrips uzeli (Zimmerman) (Thysanoptera: Phlaeothripidae) on Ficus benjamina. Pest Management Science 64: 133–140. Google Scholar


Held DW, Boyd D, Lockley T, Edwards GB. 2005. Gynaikothrips uzeli (Thysanoptera: Phlaeothripidae) in the southeastern United States: distribution and review of biology. Florida Entomologist 88: 538–540. Google Scholar


LaSalle J. 1994. North American genera of Tetrastichinae (Hymenoptera: Eulophidae). Journal of Natural History 28: 109–236. Google Scholar


Mound LA, Morris DC. 2005. Gall-inducing thrips: an evolutionary perspective, pp. 59–72 In Raman A, Schaefer CW, Withers TM [eds.], Biology, Ecology, and Evolution of Gall-Inducing Arthropods. Science Publishers, Inc., Enfield, New Hampshire. Google Scholar


Mound LA, Wang C-L, Okajima S. 1995. Observations in Taiwan on the identity of the Cuban laurel thrips (Thysanoptera, Phlaeothripidae). Journal of the New York Entomological Society 103: 185–190. Google Scholar


ThripsWiki 2015. ThripsWiki-Providing Information on the World's Thrips. (last accessed 1 Oct 2015). Google Scholar


Tree DJ. 2012. First record of Gynaikothrips uzeli (Zimmermann) (Thysanoptera: Phlaeothripidae) from Australia. Australian Entomologist 39: 105–108. Google Scholar


Tree DJ, Walter GH. 2009. Diversity of host plant relationships and leaf galling behaviours within a small genus of thrips-Gynaikothrips and Ficus in south east Queensland, Australia. Australian Journal of Entomology 48: 269–275. Google Scholar


Tree DJ, Mound LA, Field AR. 2015. Host specificity studies on Gynaikothrips (Thysanoptera: Phlaeothripidae) associated with leaf galls of cultivated Ficus (Rosales: Moraceae) trees. Florida Entomologist 98: 880–883. Google Scholar


Tyagi K. 2012. New records of Tubulifera (Thysanoptera: Phlaeothripidae) from the state of Karnataka, India. Journal of Threatened Taxa 4: 2596–2602. Google Scholar
Steven P. Arthurs, Guixin Chen, and Jianjun Chen "Host Specificity Evaluation for Gynaikothrips uzeli (Thysanoptera: Phlaeothripidae) on Ornamental Ficus (Rosales: Moraceae)," Florida Entomologist 99(3), 481-486, (1 September 2016).
Published: 1 September 2016

Back to Top