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1 March 2017 Seasonal Abundance of the Adventive Chinese Tallowtree Herbivore Caloptilia triadicae (Lepidoptera: Gracillariidae) and Its Parasitoids
G. S. Wheeler, K. Dyer, S. D. Hight, S. A. Wright
Author Affiliations +
Abstract

Chinese tallowtree, Triadica sebifera (L.) Small (Malpighiales: Euphorbiaceae), is an invasive weed from southern China that is invasive in the Gulf states of the southeastern USA. One significant factor that contributes to the success of this weed has been the lack of herbivore species attacking it in the invaded range. However, the leafminer species Caloptilia triadicae Davis (Lepidoptera: Gracillariidae) was discovered feeding on Chinese tallowtree in Florida in 2008 and has now been found throughout much of the plant's invaded range. We monitored the seasonal abundance of C. triadicae populations and their associated parasitoids over 2 yr in Florida. Populations of C. triadicae peaked in Jun and Jul in 2013 and 2014. Parasitism averaged about 3.3% of larvae and pupae, with a peak of 12%. The most abundant parasitoid species was Goniozus sp. (Hymenoptera: Bethylidae) (76% of all parasitoid individuals reared) and, second, Brasema sp. (Hymenoptera: Eupelmidae) (18% of parasitoids). Due to specific niche requirements and the apparent exploitation of leaf mines by these parasitoid species, it is doubtful they will attack species being considered for biological control of Chinese tallowtree.

Plant invasions have broad impacts on the composition of invaded communities (Mooney & Cleland 2001). Invasive plants are a new resource that may be exploited by local species with diverse trophic relations to the plant (White et al. 2006). Some of these interactions are direct, such as those between a plant and associated herbivores, but others might be indirect, as with invasive plant species linked to a variety of higher trophic-level species assemblages (Veldtman et al. 2011). Indigenous natural enemies may take advantage of recent introductions of exotic insects, although at reduced levels compared with their attack of native hosts (Cornell & Hawkins 1993). These new arrivals may be introduced either accidentally or intentionally as biological control agents. Natural enemy antagonists have been linked to the prevention of establishment or reduction of the effectiveness of species introduced for biological control of weeds (Goeden & Louda 1976; Hill & Hulley 1995; Paynter et al. 2010). Native parasitoids often exploit introduced biological control agents soon after the agents' release (Cornell & Hawkins 1993; Hill & Hulley 1995; Paynter et al. 2010; Boughton et al. 2012). Knowledge of the patterns of parasitoid attack before and following agent release may assist in directing selection of future agents that are less prone to attack (Paynter et al. 2010).

Chinese tallowtree, Triadica sebifera (L.) Small (Malpighiales: Euphorbiaceae) (= Sapium sebiferum) (hereafter “tallow”) is one of the most damaging invasive weeds in the southeastern USA, affecting wetlands, forests, and natural areas. Tallow is a deciduous tree that grows to 15 m tall in a wide range of forest types, on different soils, and under dry and moist conditions (Zheng et al. 2005). Currently, tallow infests 185,000 ha of southern forests, stranded swamps, flatwoods, and ruderal communities in areas of 10 states that border the Gulf of Mexico and in California (EDDMapS 2015; Invasive.org 2015). Costs of likely future timber losses and control over the next 20 yr in forestlands of Texas, Louisiana, and Mississippi range from $200 million to $400 million (Wang HH et al. 2012).

Most of the herbivores that feed on tallow in the USA are generalists, including the grasshoppers Melanoplus angustipennis (Dodge) and Orphulella pelidna Burmeister (Orthoptera: Acrididae) (Siemann & Rogers 2003; Lankau et al. 2004). Experimental plantings of tallow in Florida are routinely damaged by generalists including the larvae of Spodoptera frugiperda Smith & Abbot and Spodoptera latifascia Walker (Lepidoptera: Noctuidae), as well as by adults of the invasive weevils Myllocerus undatus Marshall, Pachnaeus litus (Germar), and Diaprepes abbreviatus (L.) (Coleoptera: Curculionidae) (G. S. W. unpublished data). The only specialist herbivore feeding on tallow known from the USA is the moth Caloptilia triadicae Davis (Lepidoptera: Gracillariidae), whose larvae mine and form blotches on the leaves (Davis et al. 2013). This adventive species has been reported from nearly all tallow-infested areas of the southeastern USA (Fox et al. 2012). Caloptilia triadicae is most likely from Asia and is thought to have arrived in the USA between 2002 and 2004 (Fox et al. 2012). Populations of C. triadicae were found in Florida in 2008 feeding on tallow trees planted to support biological control efforts of this invasive weed (Davis et al. 2013). Since this initial discovery, this insect has been found commonly in tallow-infested areas of Florida from early summer to Nov. During the early instars, larvae are sap feeding and form serpentine mines in young leaves. Later instars emerge from the mine and feed externally constructing a coiled, rosetteshaped leaf whorl (Fox et al. 2012; Davis et al. 2013). Mines occur on new growth, and some tallow saplings appear heavily damaged. Although C. triadicae was not introduced intentionally as a biological control agent, it shows narrow specificity completing development on only 1 other species besides the target weed (Duncan et al. 2016). Our goals were to document the seasonal abundance of this leafminer over 2 growing seasons on tallow in Florida and to document the diversity and abundance of any parasitoids attacking this herbivore's larvae or pupae.

Materials and Methods

SITES

To examine seasonal dynamics of C. triadicae, all instars and their parasitoids were monitored in a patch of planted tallow (hereafter “garden”) infested with C. triadicae near Ft. Lauderdale (Broward County; 26.084611°N, 80.240384°W), Florida, in 2013 and 2014. To supplement these collections, all instars and pupae of C. triadicae were collected in leaf whorls near Leesburg (Lake County; 28.93655°N, 81.79298°W), Gainesville (Alachua County; 29.58702°N, 82.36225°W), Tallahassee (Leon County; 30.475980°N, 84.182896°W, and 30.463672°N, 84.182167°W), and West Augustine (St John's County; 29.91619°N, 81.37440°W), Florida. All sites were infested with tallow trees that had been present for more than 20 yr.

PLANTS

Tallow plants were grown at the United States Department of Agriculture/Agricultural Research Service (USDA/ARS) Invasive Plant Research laboratory in Ft. Lauderdale, Florida, from seeds collected in Gainesville, Florida, in 2010. Their waxy coats were removed by soaking in water with laundry detergent (10 g/L) for 2 d. The prepared seeds were stored frozen (−10 °C) for 8 wk and then planted 1 cm deep in germinating media (Fafard Germinating Mix formula, Sun Gro Horticulture, Agawam, Massachusetts). Germination occurred in a screenhouse, under a 14:10 h L:D photoperiod produced by use of overhead lights (Spectralux T5 HO 54 Watt lights, Sun Blaze T5HO-48 fixtures, Sunlight Supply Inc., Vancouver, Washington). Daytime and nighttime temperatures averaged 25° C and 17° C, respectively. When the plants (n = 50) were approximately 30 to 45 cm tall, they were transferred to 3.7 or 11 L pots in potting media (Fafard 3B Professional formula Potting Mix, Sun Gro Horticulture, Agawam, MA) and moved to an outside garden. Drip irrigation was provided with 3.66 L per pot twice daily. Plants were fertilized every 2 wk with Peters Professional 20-20-20 (The Scotts Company LLC, Marysville, Ohio) at label rate and twice per year with controlled release fertilizer (Everris Nursery Mix, The Scotts Company LLC, Marysville, Ohio; 21-4-8, 22.5 g). No insecticides were applied to the plants. During insect collections, these plants were generally 1 to 1.5 m tall and had abundant newly flushed foliage.

INSECTS

To document field populations and seasonal dynamics of C. triadicae, leaf whorls were collected monthly as available during 2013 and 2014 in the tallow garden described above at Ft. Lauderdale, Florida. During each sampling, C. triadicae whorls were collected for 1 h by 1 collector and brought to the laboratory. The presence of live larvae or pupae was confirmed in each whorl by observation with a stereomicroscope (7.1× magnification). Whorls were set up individually in small Petri dishes (5.5 cm diameter) lined with moistened filter paper and sealed to the base of the Petri dish with a cotton string. Whorls were placed on a laboratory bench top at a 13:11 h L:D photoperiod and 25 °C temperature. Data were collected on the numbers of whorls collected and the numbers of C. triadicae adults and parasitoids that emerged.

Parasitoid species diversity was assessed by collecting C. triadicae larvae-infested whorls in bulk (about 250 g) from Ft Lauderdale, Gainesville, Tallahassee, and West Augustine, Florida. Whorls were placed in a large Petri dish (20 × 7 cm) lined with moistened paper. The species of parasitoids that emerged were collected and stored in 95% alcohol for identification.

Results

Host C. triadicae larvae were first sampled in May of 2013, and their density (as number per man-hour of collection effort) peaked during Jun and Jul of 2013 and 2014 (Fig. 1). Following these peaks, the density of C. triadicae larvae and pupae decreased until none was found in Oct 2013 or in Nov 2014. In total, 1,534 larvae and pupae were collected, 940 during 2013 and 594 in 2014 (Fig. 1). Adult leafminers emerged from 55.5% of these larvae or pupae. No larvae or pupae were found between Nov and May of each year as the deciduous tallow leaves were unavailable.

Parasitism occurred each year from Jun to Sep (Fig. 1). During the 2 yr of data collection, parasitism never exceeded 12% of collected larvae and pupae. Overall parasitism was 3.3%, and the most common parasitoids were a Goniozus sp. (Hymenoptera: Bethylidae) (76% of parasitoids), a Brasema sp. (Hymenoptera: Eupelmidae) (18% of parasitoids), and a Sympiesis sp. (Hymenoptera: Eulophidae) (6% of parasitoids) (Table 1; Fig. 2). Two additional parasitoid species noted were Zagrammosoma multilineatum (Ashmead) (Hymenoptera: Eulophidae) and either Euplectrus or Platyplectrus sp. (Hymenoptera: Eulophidae). When a host larva was parasitized by Goniozus sp., 3 parasitoids typically emerged from the host, whereas all of the other species were solitary.

Fig. 1.

Caloptilia triadicae larval and pupal population dynamics (A) and percentage of parasitism (B) from tallow grown in a garden in Ft. Lauderdale, Florida. Larvae and pupae were collected in leaf whorls.

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Discussion

We found that several parasitoids attacked a relatively new immigrant herbivore that has only been present in North America for about 10 yr (Fox et al. 2012). A similar parasitism pattern was found for the introduced biological control agent Neomusotima conspurcatalis Warren (Lepidoptera: Crambidae) on Lygodium microphyllum (Cav.) R. Br. (Schizeales: Lygodiaceae) (Kula et al. 2010; Boughton et al. 2012). In south Florida, 6 parasitoid species were discovered exploiting N. conspurcatalis parasitizing 6.8% of the field-collected larvae. Apparently, such novel hosts may expect only a brief period of enemy-free space before they are discovered and exploited by native natural enemies (Carvalheiro et al. 2008; Paynter et al. 2010). Over time, the diversity and density of parasitoid species exploiting the tallow leafminer in Florida is likely to increase due to its further spread or behavioral adaptation by local parasitoids (Grabenweger et al. 2010).

The parasitoids we found attacking this tallow leafminer were most likely generalists that occupied habitats near the tallow-invaded area (Cornell & Hawkins 1993). These parasitoids probably exploited hosts that feed as leafminers or species from other guilds with similar feeding habits, similar to that of the tallow-feeding C. triadicae larvae. Leafminers attacking cultivated citrus may be one source of these C. triadicae parasitoids in Florida as some of our collection sites were near the large citrus-growing areas that support the exotic citrus leafminer, Phyllocnistis citrella Stainton (Lepidoptera: Gracillariidae). Native generalists, primarily from the eulophids, attack the exotic citrus leafminer P. citrella in Florida (Peña et al. 1996; Amalin et al. 2002; Xiao et al. 2007). Our results show that at least 1 of the parasitoids associated with P. citrella, Z. multilineatum, was also recovered from the tallowfeeding leafminer C. triadicae. The introduced P. citrella parasitoid Ageniaspis citricola Logvinovskaya (Hymenoptera: Encyrtidae) was not recovered in our surveys.

Table 1.

Parasitoids reared from larvae and pupae of the leafminer Caloptilia triadicae collected feeding on Chinese tallowtree during 2013–2014 in Florida.

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Although all these parasitoids are thought to be native and to probably attack many species, their origin is unclear. However, they all attack hosts from similar feeding guilds. Brasema species are mostly primary or secondary larval/pupal ectoparasitoids of a wide variety of holometabolous insects in concealed situations (Gibson 2011). Goniozus species are ectoparasitoids of immature stages of microlepidopteran families (e.g., Gelechiidae, Pyralidae, and Tortricidae) (Gordh & Móczár 1990). Goniozus species are known to parasitize several species that occupy concealed feeding locations, such as Platynota idaeusalis Walker (Lepidoptera: Tortricidae) (Brown et al. 2010), and European grapevine moth, Lobesia botrana Denis & Schiffermüller (Lepidoptera: Tortricidae) (Moreau et al. 2010). Malaise trap surveys in central Florida detected 9 species of Goniozus (Evans & Fullerton 1997). Species of Sympiesis frequently exploit gracillariid leafminers (Grabenweger & Lethmayer 1999; Mafi & Ohbayashi 2006), including the citrus leafminer P. citrella (Schauff et al. 1998), or tortricid leafrollers (Cossentine et al. 2004).

The leafminer C. tridicae is not a classical biological control agent of tallow but was discovered in the tallow-invaded range during research conducted on the invasive weed. Due to distinctive morphological characteristics, C. tridicae is thought to have originated in Asia (Davis et al. 2013). Several unsuccessful attempts were made to find this species on tallow in China (G. S. W. unpublished data). At least 3 congeneric species were discovered feeding on tallow in its native range, causing the same distinct leaf damage. However, further analysis indicated they were not C. triadicae (Davis et al. 2013). Biological control efforts are currently focused on several species that show promise in terms of specificity and impact against tallow (Wheeler & Ding 2014). These include the flea beetle Bikasha collaris (Baly) (Coleoptera: Chrysomelidae) (Huang et al. 2011) and the defoliating caterpillar Gadirtha fusca Pogue (Lepidoptera: Nolidae) (Wang Y et al. 2012; Pogue 2014). Once released, biological control agents may come in contact with these C. triadicae parasitoids. However, it is unlikely that the niche-specific parasitoids found in this survey will attack these potential biological control agents as the larvae of B. collaris feed on tallow roots in soil and the G. fusca larvae are large (~350 mg dry weight) exposed foliage feeders. Considering the demonstrated niche specificity of these parasitoids, it is unlikely that they will attack the biological control agents being developed to control the invasive weed tallow.

Fig. 2.

Parasitoid species reared from larvae and pupae of Caloptilia triadicae feeding on Chinese tallow leaves in Florida. A. Sympiesis sp. female; B. Sympiesis sp. male (Hymenoptera: Eulophidae); C. Brasema sp. (Hymenoptera: Eupelmidae; D. Goniozus sp. (Hymenoptera: Bethylidae); E. Zagrammosoma multilineatum (Hymenoptera: Eulophidae); F. Euplectrus sp. or Platyplectrus sp. (Hymenoptera: Eulophidae). Horizontal scale bars represent 1 mm in A, B, and C and 0.5 mm in D, E, and F.

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Acknowledgments

We acknowledge W. Pierre, J. Lollis, S. Steininger, C. Nguyen, J. Duncan, and K. Bowers (USDA/ARS), who provided technical assistance. Caloptilia triadicae specimens were generously identified by D. Davis, Smithsonian Institute, Washington, District of Columbia. Assistance with parasitoid identification was generously provided by M. Gates (USDA/ARS/SEL, Beltsville, Maryland), J. Heraty (U.C. Riverside, Riverside, California), G.A.P. Gibson (Agriculture and Agri-Food Canada, Ottawa, Canada), and C. Tribull (American Museum of Natural History). DNA barcoding analysis was conducted by R. Hazen, Tulane University (GenBank accession numbers KF061045–KF061062). This research was partially funded by the Florida Fish and Wildlife Commission, Florida Department of Environmental Protection (to G. S. W.) and USDA/ARS.

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G. S. Wheeler, K. Dyer, S. D. Hight, and S. A. Wright "Seasonal Abundance of the Adventive Chinese Tallowtree Herbivore Caloptilia triadicae (Lepidoptera: Gracillariidae) and Its Parasitoids," Florida Entomologist 100(1), 52-56, (1 March 2017). https://doi.org/10.1653/024.100.0109
Published: 1 March 2017
KEYWORDS
adventive species
biological control of weeds
control biológico de malezas
especies adventivas
Gracillariidae
invasive weed
maleza invasora
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