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Comparative Parasitology 67(1) 2000 - Peru State College

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Comp. Parasitol.<br />

<strong>67</strong>(1), <strong>2000</strong> pp. 107-108<br />

Research Note<br />

New Host and Distribution Record of Gordius difficilis<br />

(Nematomorpha: Gordioidea) from a Vivid Metallic Ground Beetle,<br />

Chlaenius prasinus (Coleoptera: Carabidae) from<br />

Western Nebraska, U.S.A.<br />

BEN HANELT' AND JOHN JANOVY, JR.<br />

School of Biological Sciences, University of Nebraska-Lincoln, Lincoln, Nebraska 68588-0118, U.S.A.<br />

(e-mail: bhanelt@unlserve.unl.edu; jjanovy@unlserve.unl.edu)<br />

ABSTRACT: Gordius difficilis (Montgomery, 1898)<br />

Smith, 1994 is recorded from a creek in a juniper forest<br />

in western Nebraska. Subsequent pitfall data shows<br />

Chlaenius prasinus Dejean, 1826 to be the definitive<br />

host. This represents the first report of G. difficilis from<br />

the American Midwest, of C. prasinus as a host of<br />

nematomorphs, and as a host for G. difficilis.<br />

KEY WORDS: Gordius difficilis, Chlaenius prasinus,<br />

vivid metallic ground beetles, Nematomorpha, Nebraska,<br />

U.S.A.<br />

Nematomorphs are a well-recognized, widely<br />

distributed but poorly studied phylum (Chandler,<br />

1985). Sometimes referred to as horsehair or<br />

gordian worms, freshwater nematomorphs are<br />

obligate parasites as larvae but free-living as<br />

adults.<br />

Gordius aquaticus difficilis Montgomery,<br />

1898 was originally described from a single<br />

male specimen. Although Montgomery (1898)<br />

recognized 5 structural differences between G.<br />

aquaticus difficilis and Gordius aquaticus robustus<br />

Montgomery, 1898, he assigned G. aquaticus<br />

difficilis as a subspecies rather than a distinct<br />

species. Based on this early description,<br />

Miralles (1975) synonymized G. aquaticus difficilis<br />

with G. robustus Leidy, 1851, but Chandler<br />

(1985) synonymized G. aquaticus difficilis<br />

with Gordius paraensis Camerano, 1892.<br />

More recently, Smith (1994) used scanning<br />

electron microscopy to show that G. aquaticus<br />

difficilis is distinct enough to warrant considering<br />

it as a separate species, G. difficilis. This<br />

determination was based on the presence of a<br />

parabolic line of hairlike structures anterior to<br />

the cloacal opening, as well as the presence of<br />

distinct areoles in the midbody of the female.<br />

In mid-June 1998, G. difficilis was found in<br />

1 Corresponding author.<br />

107<br />

White Gate Creek, Keith County, Nebraska<br />

(41°12'20.5"N, 101°39'86.3"W). This site consists<br />

of a first-order, spring-fed creek suirounded<br />

by juniper trees (Juniperus scopulorum Sargent,<br />

1897) and various deciduous vegetation. The<br />

creek has a sandy bottom and often contains algal<br />

blooms because of the use of the creek by<br />

cattle. Nineteen free-living individuals were collected<br />

from the creek between late June and late<br />

July, 10 males ranging in size from 68-307 mm<br />

and 9 females ranging in size from 89-208 mm.<br />

Individuals were often found entangled in the<br />

algae or attached to sticks or rocks on the banks<br />

of the creek.<br />

In late June 1998, 4 lines of 10 pitfall traps<br />

were set adjacent to White Gate Creek. Of 6<br />

trapped Chlaenius prasinus Dejean, 1826, 2<br />

were infected with 3 worms each. None of the<br />

other invertebrates trapped contained nematomorphs.<br />

One host contained 2 female worms and<br />

1 male worm; the other host contained 3 female<br />

worms. The males ranged in size from 103-297<br />

mm, and the females ranged in size from 185-<br />

203 mm. The hosts were void of gonads, fatbodies,<br />

and intestines but appeared to behave<br />

normally.<br />

Worms were killed in 70% EtOH and brought<br />

up to 100% glycerine prior to examination. All<br />

specimens were temporarily mounted in glycerine<br />

for observation. Worms were as described<br />

by Montgomery (1898) and Smith (1994). Briefly,<br />

the male posterior is bifurcated with a subterminal<br />

ventral cloacal opening (Fig. 1). A line<br />

of hairlike structures curves around the anterior<br />

end of the cloacal opening. Posterior to the cloaca<br />

is a postcloacal crescent, extending about<br />

one-fourth the length of the lobed ends. Females<br />

have entire posteriors. Cuticular areoles are<br />

more prominent in females compared with males<br />

when viewed with light microscopy.<br />

Copyright © 2011, The Helminthological Society of Washington

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