ABSTRACT Gregarine transmission depends upon the environmental encounter rate between viable infective oocysts and suitable hosts. Many factors determine the abundance and distribution of gregarine oocysts in the environment, but the primary factors are oocyst distribution, environmental persistence, and production rate. Prior studies have demonstrated factors affecting oocyst distribution and environmental persistence, but oocyst production rate is poorly understood. This study addresses the effects of gametocyst size on oocyst production. For each of 3 gregarine species, gametocyst size was determined, and the subsequent oocyst production of each gametocyst was quantified. Gregarine species with larger gametocysts produced more oocysts per gametocyst than species with smaller gametocysts. Likewise, within species, larger gametocysts produced more oocysts. The effect was stronger in larger gregarine species, probably as a reflection of the lower overall range of gametocyst size in the smaller gregarine species.

The effects of temperature change on phospholipid content in metacercariae of Posthodiplostomum minimum and their second intermediate hosts, Lepomis macrochirus , were examined to gauge similarities in the homeoviscous adaptation of host and parasite membranes to environmental thermal change. Heart, liver, and muscle tissues from individual L. macrochirus responded to environmental temperature declines with a decrease in the ratio of phosphatidylethanolamine (PE) to phosphatidylcholine (PC). Increases in membrane PE concentration increase membrane fluidity, maintaining fish membrane function as environmental temperature declines. However, the metacercariae of P. minimum exhibit changes in cholesterol levels, total lipid levels, and lipid composition (PE/PC) that contrast the normal changes for homeoviscous membrane adaptation exhibited by their fish intermediate hosts. The parasites seem to rely on their hosts for homeoviscous adaptation within normal developmental temperature ranges, pooling both cholesterol and PE as energetic stores for development and ontological transitions signaled by elevated temperatures.

Xiphocephalus triplogemmatus n. sp. and Xiphocephalus quadratogemmatus n. sp. (Apicomplexa: Eugregarinida) are described from Eleodes tricostata and Eleodes fusiformis (Coleoptera: Tenebrionidae), respectively, collected from Keith County in the sandhills of western Nebraska. Gamonts can be diagnosed with some confidence based on relative size and shape of the deutomerite, but these taxa are distinguished by differences in oocyst size, shape, and residuua number. Together with Xiphocephalus ellisi from Eleodes opacus in the same region, X. triplogemmatus and X. quadratogemmatus form a distinct Nearctic xiphocephalid group that is morphologically distinct from groups that occur in the Palearctic, Ethiopian, and Oriental regions.

Naiadocystis phykoterion n. gen., n. sp. (Apicomplexa: Eugregarinida: Hirmocystidae), is described from the Mexican pygmy grasshopper, Paratettix mexicanus (Orthoptera: Tetrigidae), collected from sandbars along Harmon Creek, Walker County, Texas, in the western edge of the Texas Big Thicket. Naiadocystis n. gen. is distinguished by the form of the epimerite complex, a simple cordoid or toroid epimerite with an interior obconoid structure resembling a funnel that tapers to a distinct axial canal bisecting the protomerite, which is conspicuous in all stages of development, and a satellite protomerite reduced to a linearly crateriform cup or sucker that receives and enfolds posterior end of primite deutomerite. Association is precocious, caudofrontal, and biassociative. Gametocysts are spherical. Sporoducts are present but vestigial and irregular in number. Oocysts are broadly elliptoid with 4 small spherical polar knobs, 1 each at 30°, 150°, 210°, and 330°, and dehisce en masse. The species described herein are differentiated by their overall size and relative proportion of cellular structures. Naiadocystis acantholobae ( Hoshide, 1952 ) n. comb., Naiadocystis acrydiinarum ( Semans, 1939 ) n. comb., and Naiadocystis tetrigis ( Corbel, 1968 ) n. comb. are recognized as members of Naiadocystis previously placed within Gregarina (Apicomplexa: Eugregarinida: Gregarinidae).

Gregarines are common parasites of insects in culture, but no effective chemotherapeutic or prophylactic control protocol has been demonstrated. Sulfadimethoxine was administered in 5- and 7-day treatments to Death's Head cockroaches ( Blaberus discoidalis ) infected with Gregarina cubensis and Protomagalhaensia granulosae to test the efficacy of this sulfonamide against gregarine infection. Sulfadimethoxine significantly reduced the mean intensity of both G. cubensis and P. granulosae . Sulfadimethoxine treatment reduced gregarine intensity by 80% to 85% but had no significant effect on gametocyst production, suggesting that sulfonamide toxicity is directed primarily at sporozoites, trophozoites, and perhaps young gamonts. The possible use of sulfadimethoxine to produce gregarine-free insect cultures and the potential utility of gregarines as target organisms for screening pharmacologically active compounds for use against other intestinal apicomplexans are discussed.

Clitellocephalus americanus n. gen., n. sp. (Apicomplexa: Eugregarinida: Gregarinidae) is described from Cratacanthus dubius (Coleoptera: Carabidae) collected from Keith County in the Sandhills of western Nebraska. Clitellocephalus ophoni n. comb. is redescribed using original type material from Ophonus pubescens (Coleoptera: Carabidae) collected in Sète, France. Clitellocephalus n. gen. is distinguished by a deltoid epimerite with an internal anterior obconoid structure and a basal toroidal vacuole, which is retained in gamonts. Protomerites are broadly elliptical to cylindrical; deutomerites are narrowly obovate. Association is precocious, caudofrontal, and biassociative, with the satellite protomerite engulfing the posterior end of the primite deutomerite to form an interlock. Gametocysts are spherical. Sporoducts are present but reduced and irregular in number. Oocysts are dolioform, dehiscing in chains. The species described herein are differentiated by their overall size and relative proportion of cellular structures.

The host–parasite interface between 2 species of damselflies and 4 species of eugregarines was examined at the ultrastructural level. Nubenocephalus nebraskensis organisms attached to the host midgut epithelium by means of a sucker-like protomerite; the space between the epicytic folds and host epithelium was filled with electron-dense material interpreted to be adhesive in nature. Actinocephalus carrilynnae organisms attached by means of the epimerite, which had no epicytic folds, and by the fluted stalk with characteristic epicytic folds; host cell and parasite membranes appeared fused at some places on the epimerite. Hoplorhynchus acanthatholius organisms attached by means of an ovoid epimerite with backward-pointing digitations; the entire epimerite was embedded in a host cell, and host cell microvilli surrounded the stalk. Steganorhynchus dunwoodyi organisms attached by means of an ovoid stalk papilla enclosed in a retractable globular sheath; the papilla was covered with epicytic folds, but the sheath was not, and the sheath had a single membrane, whereas the epicytic folds had 2 or 3 membranes. The entire apparatus was inserted between epithelial cells, and the sheath was highly folded at its surface. The ultrastructural observations suggest that actinocephalid gregarines have evolved 2 general strategies for attaching to the host epithelium, that is, suckerlike protomerites, as in the case of N. nebraskensis, and deeply embedded epimerites inserted within or between host cells, as in the other species studied.