Translator Disclaimer
1 December 2015 First Report of an Egg Parasitoid Reared from Neomusotima conspurcatalis (Lepidoptera: Crambidae), A Biological Control Agent of Lygodium microphyllum (Schizaeales: Lygodiaceae)
Author Affiliations +

Native predators and parasitoids within the introduced range of a biological control agent often find and attack the agent, a novel resource (Hill & Hulley 1995; Paynter et al. 2010; Christensen et al. 2011). Biotic interference or resistance can decrease the efficacy of a biological control agent, and may even prevent biological control agents from establishing in the introduced range (Goeden & Louda 1976; Van Driesche et al. 2008 and references therein; Paynter et al. 2010). For example, predation by the generalist Plagiognathus politis Uhler (Hemiptera: Miridae) decreased the effectiveness of Galerucella calmariensis L. (Coleoptera: Chrysomelidae), on Lythrum salicaria L. (Myrtales: Lythraceae), purple loosestrife, and predation by spiders, fire ants, and birds contributed to the failure of Spodoptera pectinicornis Hampson (Lepidoptera: Noctuidae) to establish on Pistia stratiotes L. (Alismatales: Araceae), waterlettuce (Dray et al. 2001; Hunt-Joshi & Blossey 2005).

Old World climbing fern, Lygodium microphyllum (Cavanilles) R. Brown (Schizaeales: Lygodiaceae), is native to tropical and subtropical regions of the Old World (Pemberton 1998; Smith et al. 2006). It escaped cultivation in Florida and was first reported as naturalized in 1965 (Beckner 1968; Pemberton & Ferriter 1998). Lygodium microphyllum is now widespread in wetland and mesic habitats in south and central Florida, with several isolated populations in north Florida (EDDMaps 2015). This aggressive indeterminate vine can climb 20 m or more into trees and can extend horizontally, smothering native vegetation and reducing plant diversity and ecosystem services (Gordon 1998; Pemberton & Ferriter 1998). Lygodium microphyllum produces vast numbers of spores that are windborne and opportunistically selfcompatible (Lott et al. 2003; Volin et al. 2004).

The rapid spread of L. microphyllum, its impact on native communities, and the lack of effective long-term control using conventional management techniques prompted the start of a classical biological control program in 1997 (Goolsby et al. 2003; Hutchinson et al. 2006). The ongoing search for potential biological control agents has focused on Asia and Australia (Pemberton 1998; Goolsby et al. 2003).

The moth Neomusotima conspurcatalis Warren (Lepidoptera: Crambidae) was approved for release as a biological control agent of L. microphyllum in 2007 (Boughton & Pemberton 2009). Field releases began in 2008 and large populations developed quickly at some sites causing “brown out” events where heavy defoliation by the larvae caused large areas of L. microphyllum to turn brown (Boughton & Pemberton 2009). Field collections of N. conspurcatalis larvae to check for parasitism began approximately 8 mo after the first release (Boughton et al. 2012). In total, 1,100 N. conspurcatalis larvae were collected from Jonathan Dickinson State Park, Hobe Sound, Florida, USA, between 2008 and 2010 (Boughton et al. 2012). Four species of hymenopteran and one species of dipteran parasitoids were reared from these larvae (Kula et al. 2010; Boughton et al. 2012).

Here we report the first egg parasitoid reared from N. conspurcatalis in its introduced range. This is the first recorded egg parasitoid for Neomusotima at the generic level (Noyes 2015). Neomusotima conspurcatalis females lay eggs singly or in clutches of 20 or more eggs, usually on the underside of L. microphyllum foliage (Solis et al. 2004; Boughton & Pemberton 2012; personal observation). The eggs are relatively flat, may overlap like shingles, and are translucent pale yellow in color (Solis et al. 2004; Boughton & Pemberton 2012; personal observation). The egg turns more yellow as the larva develops, and the dark head capsule becomes visible before the 2 mm long larva emerges. Healthy egg masses are difficult to see with the naked eye due to their color and small size. In contrast, parasitized egg masses are more visible because the chorion of parasitized eggs turns a grayish color with black spots, making these egg masses stand out against the L. microphyllum foliage. In Mar 2013, a dark N. conspurcatalis egg mass was observed on L. microphyllum collected from a field site in Martin County, Florida, USA. This egg mass was held in the laboratory and microhymenopterans emerged.

Parasitized egg masses have since been recovered at multiple sites located up to 125 km apart in southeast Florida. These egg masses were found by observers searching foliage in the field or were detected in the laboratory on field-collected L. microphyllum that was examined visually prior to use in the N. conspurcatalis mass rearing operation. Individual parasitized egg masses were left in situ on foliage of L. microphyllum and held in a plastic vial (Thorton Plastics CO, Salt Lake City, Utah, USA) at approximately 24 °C until parasitoids emerged. The microhymenopterans and remains of the egg mass were then preserved in 95% ethanol and sent to the U.S. Department of Agriculture, Agricultural Research Service, Systematic Entomology Labora tory for identification. Males were identified by antennal features, and slide mounts were made using the methods outlined by Platner et al. (1999). Specimens collected from 2 sites in south Florida (26.070815°N, 80.277655°W; 25.958249°N, 80.340957°W) were identified as Trichogramma sp. (Hymenoptera: Trichogrammatidae) using Pinto (1997).

Subsequently, specimens were keyed through the revision of North American species of Trichogramma (Pinto 1999), but a satisfactory result was not obtained. Additional males are needed, particularly larger specimens, in order to observe the ridges and processes of the genital capsule (via scanning electron microscopy) that are difficult to discern with slide mounted material (Pinto 1999). Further, additional slide mounts will allow for accurate determination of the presence of basiconic peg sensilla on the flagellum (Pinto 1999). With the continued efforts outlined above, we hope to arrive at a positive identification. However, it may be that this species is extralimital or, possibly, new. In either case, the results would be reported separately.

Trichogrammatid wasps are egg parasitoids and the genus Trichogramma includes numerous biological control agents (Triplehorn & Johnson 2005). Multiple eggs within a single N. conspurcatalis egg mass are often parasitized and parasitism rates can reach 100%. Parasitism rates by Trichogramma species can vary depending on environmental conditions, such as temperature and humidity, and by host density (Bourchier & Smith 1996; Quayle et al. 2003; Kalyebi et al. 2005). Romeis et al. (2005) reviewed additional factors that can alter parasitism rates by Trichogramma, including habitat type and host food plant species and structure. Further research is needed to determine how these factors influence the interaction between N. conspurcatalis and its Trichogramma sp. parasitoid. It also remains unclear how parasitism affects the population dynamics of N. conspurcatalis and its efficacy as a biological control agent of L. microphyllum.

We thank the many land managers who permitted us to conduct research on their L. microphyllum populations. Tracey Wasylik, Alex Chapman, and Cristina Martinez provided assistance in the field and laboratory. Mention of trade names or commercial products in this publication is solely for the purpose of providing specific information and does not imply recommendation or endorsement by the U.S. Department of Agriculture (USDA). USDA is an equal opportunity provider and employer. Funding was provided by the South Florida Water Management District and the U.S. Army Corps of Engineers as part of the Comprehensive Everglades Restoration Plan (CERP).

Summary

Neomusotima conspurcatalis Warren (Lepidoptera: Crambidae) was first released in Florida, USA, as a biological control agent of Lygodium microphyllum (Cavanilles) R. Brown (Schizaeales: Lygodiaceae), Old World climbing fern, in 2008. The first egg parasitoid, a Trichogramma sp. (Hymenoptera: Trichogrammatidae), was reared from N. conspurcatalis in 2013. The parasitoid is widely distributed in south Florida, where its egg mass parasitism rates can reach 100%.

Key Words: egg parasitism; Trichogramma; Old World climbing fern; weed biological control

Sumario

Neomusotima conspurcatalis Warren (Lepidoptera: Crambidae) fue liberado por primera vez en la Florida, EE.UU., como un agente de control biológico de Lygodium microphyllum (Cavanilles) R. Brown (Polypodiales: Lygodiaceae), el helecho trepador del Viejo Mundo, en 2008. El primer parasitoide de huevos, un Trichogramma sp., fue criado de N. conspurcatalis en 2013. El parasitoide se distribuye ampliamente en el sur de Florida, donde sus tasas de parasitismo de masas de huevos pueden llegar al 100%.

Palabras Clave: parasitismo de huevos; Trichogramma; helecho trepador de Viejo Mundo; control biológico de malezas

References Cited

1.

J Beckner . 1968. Lygodium microphyllum, another fern escaped in Florida. American Fern Journal 55: 93–94. Google Scholar

2.

AJ Boughton , RW Pemberton . 2009. Establishment of an imported natural enemy, Neomusotima conspurcatalis (Lepidoptera: Crambidae) against an invasive weed, Old World climbing fern, Lygodium microphyllum, in Florida. Biological Control Science and Technology 19: 769–772. Google Scholar

3.

AJ Boughton , RW Pemberton . 2012. Biology and reproductive parameters of the brown lygodium moth, Neomusotima conspurcatalis—a new biological control agent of Old World climbing fern in Florida. Environmental Entomology 41: 308–316. Google Scholar

4.

AJ Boughton , RR Kula , M Gates , Y Zhang , M Nunez , J O'Connor , JB Whitfield , TD Center . 2012. Parasitoids attacking larvae of a recently introduced weed biological control agent, Neomusotima conspurcatalis (Lepidoptera: Crambidae): key to species, natural history, and integrative taxonomy. Annals of the Entomological Society of America 105: 753–767. Google Scholar

5.

RS Bourchier , SM Smith . 1996. Influence of environmental conditions and parasitoid quality on field performance of Trichogramma minutum. Entomologia Experimentalis et Applicata 80: 461–468. Google Scholar

6.

RM Christensen , PD Pratt , SL Costello , MB Rayamajhi , TD Center . 2011. Acquired natural enemies of the weed biological control agent Oxyops vitiosa (Coleoptera: Curculionidae). Florida Entomologist 94: 1–8. Google Scholar

7.

FA Dray Jr , TD Center , GS Wheeler . 2001. Lessons from unsuccessful attempts to establish Spodoptera pectinicornis (Lepidoptera: Noctuidae), a biological control agent of waterlettuce. Biocontrol Science and Technology 11: 301–316. Google Scholar

8.

EDDMaps. 2015. Center for Invasive Species and Ecosystem Health: Early Detection and Distribution Mapping System, University of Georgia,  https://www.eddmaps.org/distribution/viewmap.cfm?sub=3046 (last accessed 29 Jun 2015). Google Scholar

9.

RD Goeden , SM Louda . 1976. Biotic interference with insects imported for weed control. Annual Review of Entomology 21: 325–342. Google Scholar

10.

JA Goolsby , AD Wright , RW Pemberton . 2003. Exploratory surveys in Australia and Asia for natural enemies of Old World climbing fern, Lygodium microphyllum: Lygodiaceae. Biological Control 28: 33–46. Google Scholar

11.

DR Gordon . 1998. Effects of invasive, non-indigenous plant species on ecosystem processes: lessons from Florida. Ecological Applications 8: 975–989. Google Scholar

12.

MP Hill , PE Hulley . 1995. Host-range extension by native parasitoids to weed biocontrol agents introduced to South Africa. Biological Control 5: 297–302. Google Scholar

13.

TR Hunt-Joshi , B Blossey . 2005. Interactions of root and leaf herbivores on purple loosestrife (Lythrum salicaria). Oecologia 142: 554–563. Google Scholar

14.

JA Hutchinson , A Ferriter , K Serbesoff-King , K Langeland , L Rodgers [eds.]. 2006. Old World Climbing Fern (Lygodium microphyllum) Management Plan for Florida, 2nd edition. Florida Exotic Pest Plant Council Lygodium Task Force, Florida, USA. Google Scholar

15.

A Kalyebi , WA Overholt , F Schulthess , JM Mueke , SA Hassan , S Sithanantham . 2005. Functional response of six indigenous trichogrammatid egg parasitoids (Hymenoptera: Trichogrammatidae) in Kenya: the influence of temperature and relative humidity. Biological Control 32: 164–171. Google Scholar

16.

RR Kula , AJ Boughton , RW Pemberton . 2010. Stantonia pallida (Ashmead) (Hymenoptera: Braconidae) reared from Neomusotima conspurcatalis Warren (Lepidoptera: Crambidae), a classical biological control agent of Lygodium microphyllum (Cav.) R. Br. (Polypodiales: Lygodiaceae). Proceedings of the Entomological Society of Washington 112: 61–68. Google Scholar

17.

MS Lott , JC Volin , RW Pemberton , DF Austin . 2003. The reproductive biology of the invasive ferns Lygodium microphyllum and L. japonicum (Schizaeaceae): implications for invasive potential. American Journal of Botany 90: 1144– 1152. Google Scholar

18.

JS Noyes . 2015. Universal Chalcidoidea Database,  http://www.nhm.ac.uk/chalcidoids (last accessed 7 Jul 2015). Google Scholar

19.

Q Paynter , SV Fowler , AH Gourlay , R Groenteman , PG Peterson , L Smith , CJ Winks . 2010. Predicting parasitoid accumulation on biological control agents of weeds. Journal of Applied Ecology 47: 575–582. Google Scholar

20.

RW Pemberton . 1998. The potential of biological control to manage Old World climbing fern (Lygodium microphyllum), an invasive weed in Florida. American Fern Journal 88: 176–182. Google Scholar

21.

RW Pemberton , AP Ferriter . 1998. Old World climbing fern (Lygodium microphyllum), a dangerous invasive weed in Florida. American Fern Journal 88: 165–175. Google Scholar

22.

JD Pinto . 1997. Trichogrammatidae, pp. 726–752 In GAP Gibson , JT Huber , JB Woolley [eds.], Annotated Keys to the Genera of Nearctic Chalcidoidea (Hymenoptera). National Research Council Canada, NRC Research Press, Ottawa, Ontario, Canada. Google Scholar

23.

JD Pinto . 1999. Systematics of the North American species of Trichogramma Westwood (Hymenoptera: Trichogrammatidae). Memoirs of the Entomological Society of Washington 22: 287. Google Scholar

24.

GR Platner , RK Velten , M Planoutene , JD Pinto . 1999. Slide-mounting techniques for Trichogramma (Trichogrammatidae) and other minute parasitic Hymenoptera. Entomological News 110: 56–64. Google Scholar

25.

D Quayle , J Régnière , N Cappuccino , A Dupont . 2003. Forest composition, hostpopulation density, and parasitism of spruce budworm Choristoneura fumiferana eggs by Trichogramma minutum. Entomologia Experimentalis et Applicata 107: 215–227. Google Scholar

26.

J Romeis , D Babendreier , FL Wäcker , TG Shanower . 2005. Habitat and plant specificity of Trichogramma egg parasitoids—underlying mechanisms and implications. Basic and Applied Ecology 6: 215–236. Google Scholar

27.

AR Smith , KM Pryer , E Schuettpelz , P Korall , H Schneider , PG Wolf . 2006. A classification for extant ferns. Taxon 55: 705–731. Google Scholar

28.

MA Solis , S Yen , JH Goolsby . 2004. Species of Lygomusotima new genus and Neomusotima Yoshiyasu (Lepidoptera: Crambidae) from Australia and southeastern Asia feeding on Lygodium microphyllum (Schizaeaceae). Annals of the Entomological Society of America 97: 64–76. Google Scholar

29.

CA Triplehorn , NF Johnson . 2005. Borror and DeLong's Introduction to the Study of Insects, 7th edition. Thomson Brooks/Cole, Belmont, California, USA. Google Scholar

30.

Driesche R Van , M Hoddle , T Center . 2008. Control of Pests and Weeds by Natural Enemies: An Introduction to biological control. Blackwell Publishing Ltd., Malden, Massachusetts, USA. Google Scholar

31.

JC Volin , MS Lott , JD Muss , D Owen . 2004. Predicting rapid invasion of the Florida Everglades by Old World climbing fern (Lygodium microphyllum). Diversity and Distributions 10: 439–446. Google Scholar
Ellen C. Lake, Michael W. Gates, Melissa C. Smith, Gloria L. Witkus, and Paul D. Pratt "First Report of an Egg Parasitoid Reared from Neomusotima conspurcatalis (Lepidoptera: Crambidae), A Biological Control Agent of Lygodium microphyllum (Schizaeales: Lygodiaceae)," Florida Entomologist 98(4), 1244-1246, (1 December 2015). https://doi.org/10.1653/024.098.0436
Published: 1 December 2015
JOURNAL ARTICLE
3 PAGES


SHARE
ARTICLE IMPACT
Back to Top