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1 March 2007 POLYPEDILUM NUBIFER, A CHIRONOMID MIDGE (DIPTERA: CHIRONOMIDAE) NEW TO FLORIDA THAT HAS NUISANCE POTENTIAL
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In 2001, Everglades National Park (ENP), United States Department of the Interior, initiated a biomonitoring program incorporating fish and invertebrate sampling to monitor water quality entering the Park, and to detect exotic species. Midges (Diptera: Chironomidae and Ceratopogonidae) were sampled by collecting their floating pupal exuviae according to standard United States Environmental Protection Agency (USEPA) protocols (Ferrington et al. 1991). Samples collected in early Oct 2002 from two recently constructed 242-hectare and 324-hectare detention ponds along the eastern boundary of ENP (Ponds 332C and 332D, Fig. 1) yielded large numbers of pupal exuviae, larval exuviae, and spent adults of Polypedilum nubifer (Skuse). Additional pupal exuviae and adults were collected near these ponds in shallow solution depressions within ENP. This is the first record of P. nubifer in Pan-America, and is particularly noteworthy considering its capacity to reach nuisance population levels in Asia and Australia (Ali 1995; Cranston & Martin 1989; Sasa & Sublette 1980; Traylor et al. 1994; Wang 2000) and its potential for causing similar problems in Florida.

Adults of P. nubifer can be distinguished from other congenerics by the distinctive spotting pattern on the wings and the characteristic configuration of the male hypopygium (Sasa & Sublette 1980). Pupae possess an unusually large, uneven, multiple-toothed anal comb, extensive shagreen on tergites II-VI, and short, pointed cephalic tubercles (Cranston 2000; Sasa & Sublette 1980). The alternating Lauterborn organs on the larval antenna are unique for the genus.

Polypedilum nubifer is a common, eurytopic midge in tropical and subtropical waters in the Afrotropical, Palaearctic, Oriental, and Australasian regions. Populations can become extremely abundant in warm, shallow, eutrophic waters subject to seasonal drying (Cranston 2000). Consequently, emerged adults from many artificial or altered habitats such as rice fields, eel ponds, drainage channels, canals, and treatment ponds, often pose a considerable nuisance to people living nearby (Sasa & Sublette 1980; Wang 2000). The larvae are also considered a major pest of rice fields in China, damaging the roots and leaves of rice seedlings (Wang 2000). Presumably introduced into Hawaii during World War II, mass emergences of P. nubifer have become a serious problem to residents near Kealia Pond National Wildlife Refuge in Maui (M. B. Berg, Dept. of Biology, Loyola Univ. of Chicago, personal communication).

Introductions of non-native chironomid midges through air or sea transport are probably common, but instances of their occurrence are difficult to ascertain with confidence because many species are widely distributed, and our understanding of regional midge faunas and the distributions of species is generally poor. The most plausible cases of human-mediated midge introductions involve the appearance of large, pestiferous populations of previously uncollected species in a region where the midge fauna has been fairly well studied (Spies 2000). Our observations of large populations of P. nubifer from Florida, a state whose chironomid fauna has been relatively well documented (Epler 1995, 2001), lead us to suspect that it is a recent arrival to south Florida. Other extraneous species in the Nearctic include Goeldichironomus amazonicus (Fittkau) in Florida and southern California (Wirth 1979; Sublette & Mulla 1991), and Chironomus strenzkei Fittkau in southern California (Sublette & Mulla 2000). Both species are thought to be recent introductions from the Neotropics, joining other suspected earlier Neotropical migrants such as Chironomus anonymus Williston (Wülker et al. 1989), and Chironomus calligraphus Goeldi (Sublette & Mulla 2000), that have flourished in eurythermal, eutrophic, and usually human-engineered aquatic habitats in the southern Nearctic (Spies et al. 2002).

The artificial ponds where P. nubifer was collected, called detention ponds 332C and 332D, are 2 of a series of shallow infiltration basins constructed by the U.S. Army Corps of Engineers in 2001 and 2002 for maintaining suitable water levels for breeding populations of the endangered Cape Sable Seaside Sparrow (Ammodramus maritimus mirabilis) in eastern ENP. Water from the L-31N canal, which transects agricultural areas in southern Miami-Dade County, is periodically pumped into these shallow basins to a depth of approximately 1.0 m and allowed to percolate through the porous limestone bedrock. The resulting locally-elevated water table reduces the flux of groundwater eastward out of ENP. The successive cycles of flooding with water from the L-31N canal, and subsequent drydowns, concentrate nutrients in these basins during their operation period. Soil samples collected at the time of midge sampling showed total phosphorus levels (EPA 3050 method) in detention pond soils ranged from 581 ppm in 332B to 1579 ppm in 332C, whereas soils from neighboring marshes in ENP had total phosphorus concentrations from 221-288 ppm. At drydown, elevated water temperatures and solute concentrations, and accumulation of fine organic and inorganic sediments may provide ideal conditions for warm-adapted species with broad ecological requirements and environmental tolerances to thrive. The fauna of both detention ponds (Table 1) were dominated by potentially pestiferous taxa such as Apedilum elachistum Townes, A. subcinctum Townes, and P. nubifer (Table 13.1 in Ali 1995). Collections of pupal exuviae in primarily open-water habitats do not allow one to estimate the magnitude of emergence on an areal basis. However, windrows of exuviae were evident along leeward shorelines, and 10 dips with a 3-quart pot within a bed of floating macrophytes in Pond 332C yielded an estimated 24,000 chironomid pupal exuviae, 76.4% of which were P. nubifer. A similar sample from Pond 332D had an estimated 23,000 pupal exuviae, of which 1.6% were P. nubifer. Samples (about 2 m2 surface area) from vegetated solution depressions located 50 m, 250 m, and 3 km to the west of Pond 332C yielded 6, 1, and 0 pupal exuviae of P. nubifer, respectively.

The observed populations of P. nubifer are in sparsely inhabited agricultural areas 5 miles west of the City of Homestead and currently not a nuisance problem. Collections of P. nubifer pupal exuviae in solution depressions in ENP indicate that this species is capable of surviving in Everglades marshes, but their low numbers in these depressions relative to those in the detention ponds suggest that there is a low likelihood that they will flourish and displace native species under the current high water quality conditions present in ENP. Samples collected in 2003, 2004, and 2005 from ENP marshes near 332C and 332D did not yield any P. nubifer pupal exuviae. However, continued monitoring of the midge fauna along the perimeter of ENP will be necessary to confirm the non-invasive status of this species. Considering the warm climate, and the variety of intermittent, enriched, and shallow-water habitats present in south Florida, the potential exists for P. nubifer to reach nuisance levels in urban or agricultural areas in the future.

We thank Cristina Bruno, Marcos Gomes, Jeff Kline, Lorena Morales, and Florian Veau for assisting in sample collection. We thank Quan Dong, William Coffman, Richard Lobinsky, and two anonymous reviewers for commenting on earlier drafts of this manuscript. This contribution is part of a larger study of invertebrates in Everglades National Park that was funded by the Critical Ecosystems Science Initiative of the National Park Service.

Summary

We document the first record of Polypedilum nubifer in Pan-America. This eurytopic species often reaches severe nuisance population sizes in Australia, Asia, and Hawaii in warm, shallow, eutrophic waters subject to drying. A large population was discovered in newly-constructed infiltration basins and neighboring marshes along the eastern boundary of Everglades National Park. Presently, this population appears minimally invasive to Park marshes and is far removed from urban areas. However, we anticipate this species could disperse and attain nuisance population sizes in suitable urban and agricultural habitats in south Florida.

References Cited

1.

A. Ali 1995. Nuisance, economic impact and possibilities for control. pp. 339-364 In P. D. Armitage, P. S. Cranston, and L. C. V. Pinder [eds.],The Chironomidae. The Biology and Ecology of Non-biting Midges. Chapman Hall, London. 572 pp. Google Scholar

2.

P. S. Cranston 2000. Electronic identification guide to the Australian Chironomidae.  http://entomology.ucdavis.edu/chiropage/Google Scholar

3.

P. S. Cranston and J. Martin . 1989. Family Chironomidae pp. 252-74 In N. L. Evenhuis [ed.], Catalog of the Diptera of the Australasian and Oceanian Regions. Bishop Museum Press, Honolulu and E. J. Brill, Leiden. 1155 pp. Google Scholar

4.

J. H. Epler 1995. Identification Manual for the Larval Chironomidae (Diptera) of Florida. Revised edition. Florida Dept. Environmental Protection, Tallahassee, FL. 317 pp. Google Scholar

5.

J. H. Epler 2001. Identification Manual for the Larval Chironomidae (Diptera) of North and South Carolina. A Guide to the Taxonomy of the Midges of the Southeastern United States, Including Florida. Special Publication SJ2001-SP13. North Carolina Department of Environment and Natural Resources, Raleigh, NC, and St. Johns River Water Management District, Palatka, FL. 526 pp. Google Scholar

6.

L. C. Ferrington Jr., M. A. Blackwood, N. H. Crisp, J. L. Kavanaugh, and F. J. Schmidt . 1991. A protocol for using surface-floating pupal exuviae of Chironomidae for rapid bioassessment of changing water quality. pp. 181-190 In Sediment and stream water quality in a changing environment: trends and explanation. Proc. Vienna Symposium. International Association of Hydrological Sciences Publ. No. 203. Google Scholar

7.

M. Sasa and J. E. Sublette . 1980. Synonymy, distribution, and morphological notes on Polypedilum (s. s.) nubifer (Skuse) (Diptera: Chironomidae). Japanese J. Sanit. Zool 31:93–102. Google Scholar

8.

M. Spies 2000. Non-biting ‘nuisance’ midges (Diptera, Chironomidae) in urban southern California, with notes on taxonomy, ecology and zoogeography. pp. 621-628 In O. Hoffrichter [ed.], Late 20th Century Research on Chironomidae: An Anthology from the 13th International Symposium on Chironomidae. Shaker, Aachen, 661 pp. Google Scholar

9.

M. Spies, J. E. Sublette, M. F. Sublette, W. F. Wülker, J. Martin, A. Hille, M. A. Miller, and K. Witt . 2002. Pan-american Chironomus calligraphus Goeldi, 1905 (Diptera, Chironomidae): species or complex? Evidence from external morphology, karyology and DNA sequencing. Aquat. Insects 24:91–113. Google Scholar

10.

J. E. Sublette and M. S. Mulla . 1991. Goeldichironomus amazonicus (Diptera: Chironomidae), a potentially pestiferous midge recently discovered in California. Entomol. News 102:47–49. Google Scholar

11.

J. E. Sublette and M. S. Mulla . 2000. Chironomus strenzkei Fittkau--a new Pan-American distribution, with a review of recent similar additions to the Nearctic midges (Insecta, Diptera, Chironomidae). pp. 145-149 In M. Baehr and M. Spies [eds.], Contributions to Chironomid Research in Memory of Dr. Friedrich Reiss. Spixiana 23. Google Scholar

12.

K. M. Traylor, A. M. Pinder, and J. A. Davis . 1994. Evaluation of the juvenile hormone mimic pyriproxyfen (S-31183) against nuisance chironomids (Diptera: Chironomidae), with particular emphasis on Polypedilum nubifer (Skuse). J. Australian Entomol. Soc 33:127–130. Google Scholar

13.

X. Wang 2000. Nuisance chironomid midges recorded from China (Diptera). pp. 653-658 In O. Hoffrichter [ed.], Late 20th Century Research on Chironomidae: An Anthology from the 13th International Symposium on Chironomidae. Shaker, Aachen, 661 pp. Google Scholar

14.

W. W. Wirth 1979. Siolimyia amazonica Fittkau, an aquatic midge new to Florida with nuisance potential. Florida Entomol 62:134–135. Google Scholar

15.

W. Wülker, J. E. Sublette, E. Morath, and J. Martin . 1989. Chironomus columbiensis n. sp. in South America and Chironomus anonymus Williston in North America--closely related species. Stud. Neotropical Fauna and Envir 24:121–136. Google Scholar

Appendices

Fig. 1.

Locations of detention ponds 332C and 332D along the eastern boundary of Everglades National Park.

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Table 1. Percent relative abundance of chironomidae and ceratopogonidae species in pupal exuviae samples from detention ponds 332C and 332D adjacent to everglades national park on 7 oct 2002. X = rare (<0.1%), - = absent.

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Richard E. Jacobsen and Sue A. Perry "POLYPEDILUM NUBIFER, A CHIRONOMID MIDGE (DIPTERA: CHIRONOMIDAE) NEW TO FLORIDA THAT HAS NUISANCE POTENTIAL," Florida Entomologist 90(1), 264-267, (1 March 2007). https://doi.org/10.1653/0015-4040(2007)90[264:PNACMD]2.0.CO;2
Published: 1 March 2007
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