Cytology of Leidyana canadensis (apicomplexa: eugregarinida) in Lambdina fiscellaria fiscellaria larvae (lepidoptera: geometridae)

The eugregarine Leidyana canadensis infects the larval gut of the eastern hemlock looper, Lambdina fiscellaria fiscellaria. Guts of infected larvae were chemically fixed, embedded in epoxy resin, and sectioned for light and electron microscopy to describe the cytology of L. canadensis and its pathology in the larval host. Oocysts of L. canadensis are ingested by larval hemlock looper. Trophozoites emerge from the oocysts, pass through the peritrophic membrane into the ectoperitrophic space, and attach to the epithelium of the midgut by means of an apical epimerite. The epimerite does not actually penetrate the affected epithelial cell; instead, it causes an invagination of the plasma membrane of the cell. The center of the epimerite contains membrane cisternae, and mitochondria line its periphery. Microtubules and mitochondria in the host cell cytoplasm surround the epimerite. At the light microscopic level, there appeared to be septa between the epimerite and the protomerite and between the protomerite and the deutomerite; however, in the electron microscope, no septa were evident. Only differences in the concentrations and nature of the inclusions in the cytoplasms of these three regions were apparent. The deutomerite contains a single nucleus in the central-posterior area. After an undetermined period, the epimerite detaches from the host gut epithelium and is withdrawn into the protomerite, and the trophozoites float freely in the ectoperitrophic space before differentiating into gamonts. Division of the single, large nucleus into numerous small nuclei appears to occur prior to syzygy. Gamonts pair and a cyst wall is laid down around them, forming a gametocyst. Oocysts are extruded from mature gametocysts, in chains, through sporoducts.     

Two New Menosporine Gregarines, Hoplorhynchus acanthatholius N. Sp. and Steganorhynchus dunwoodyi N. G., N. Sp. (Apicomplexa: Eugregarinorida: Actinocephalidae) from Coenagrionid Damselflies (Odonata: Zygoptera)

ABSTRACT. Hoplorhynchus acanthatholius , n. sp. is described from Enallagma civile , the Civil Bluet damselfly. Trophozoites are solitary, lie in the mesenteron between the peritrophic membrane and the epithelium, and attain a maximum length of 850 μm. Epimerite ovoid to broadly ovoid; anterior margin bearing eight equidistant retroarcuate hooks; attached to protomerite by means of a vermicular stalk. Protomerite ovoid; deutomerite narrowly obvoid. Gametocysts spherical; diam 300 μm, sporulating by simple dehiscence in 48–72 h. Oocysts are characteristic of Menosporinae: smooth, biconical, crcscentic, uniform in size and shape. Steganorhynchus dunwoodyi , n. g., n. sp. is described from the damselfly Ischnura verticalis. The genus is characterized by an epimerite comprising an ovoid papilla enclosed in a retractable, globular sheath, borne on a long vermicular stalk. Trophozoites are solitary, lie in the mesenteron between the peritrophic membrane and epithelium, and attain a maximum length of 605 μm. Protomerite very broadly ovoid; deutomerite obvoid. Gametocysts spherical; diam 258 μm, sporulating by simple dehiscence in 48–72 h. Oocysts are characteristic of Menosporinae: smooth, biconical, crescentic, uniform in size and shape. The population dynamics of H. acanthatholius and S. dunwoodyi among damselfly populations in five Nebraska localities are presented.     

Gregarina coronata N. Sp. (Apicomplexa: Eugregarinida) Described from Adults of the Southern Corn Rootworm, Diabrotica undecimpunctata howardi (Coleoptera: Chrysomelidae)

ABSTRACT. Gregarina coronata n. sp. (Apicomplexa: Eugregarinida) is described from the adults of the Southern Corn Root Worm, Diabrotica undecimpunctata howardi (Coleoptera: Chrysomelidae). Measurements given are means, in micrometers, taken from mature gamonts in association. Primite: protomerite hemi-ellipsoidal with basal tumidus, length 47.6, width 44.0, with cytoplasmic granule, apical crown apparent; deutomerite elongate ellipsoidal, length 227.9, width 81.3; epimerite absorbed into anterior in gamont, globular in trophozoite. Satellite: protomerite hemi-ellipsoidal, truncated at association interface to appear trapezoidal, length 39.2, width 49.6, with cytoplasmic granule; deutomerite elongate ellipsoidal, length 240.6, width 80.2; epimerite absorbed into anterior in gamont. Association caudofrontal and often precocious, occurring during growth of trophozoites. Gametocysts spherical, 115.3 in diameter, 132.9 with hyaline coat; producing multiple oocyst chains under moist storage in 24–36 h. Oocysts very uniform in shape and size, dorsad: doliform, length 6.4, equatorial width 3.4, polar width 2.9; pleuron: dorso-ventrally flattened, corpus concave with bicondylic termina; corpus height 0.98, width 4.44; terminus height 1.96, width 0.98.     

Eugregarine trophozoite detachment from the host epithelium via epimerite retraction: Fiction or fact?

Eugregarines represent a diverse group of Apicomplexa parasitising numerous invertebrates. Their sporozoites generally develop into epicellular trophozoites attached to the host epithelium by a specialised attachment organelle known as an epimerite. They are considered peculiar protists due to their unique cell architecture and dimensions as well as their attachment strategy which is similar to that of cryptosporidia. Using electron and fluorescence microscopy, the fine structure of the epimerite with associated structures and the mechanism of trophozoite detachment from the host epithelium were studied in Gregarina polymorpha parasitising the intestine of Tenebrio molitor larvae. The epimerite appears to be a very dynamic structure whose shape dramatically changes depending on whether or not it is embedded into the host epithelium. The trophozoite’s most fragile zone is the area below the membrane fusion site at the epimerite base. The epimerite plasma membrane forms basal radial ribs which are involved in increasing its surface and strengthening the epimerite-host cell junction. FITC-phalloidin labelling demonstrated the presence of filamentous actin in trophozoites along with its accumulation at the epimerite base and in the apical end of the protomerite, as well as a patch accumulation of filamentous actin in the protomerite of maturing and mature trophozoites. Indirect immunofluorescence revealed the presence of myosin in the cortical zone of the epimerite and in the membrane fusion site area. The data obtained strongly suggest that these structures could facilitate the detachment of a mature trophozoite from the host epithelium. Supported by data presented herein and our previous observations, we propose a new hypothesis on the mechanism of trophozoite detachment from the host epithelium based on epimerite retraction into the protomerite. This is contrary to the commonly accepted hypothesis describing gradual epimerite constriction and subsequent separation facilitated by contractility of the membrane fusion site (osmiophilic ring).     

Studies on the Early Development of the Eugregarine Gregarina garnhami

SYNOPSIS. The Eugregarine Gregarina garnhami is parasitic in the mid-intestine and caecae of the desert locust Schistocerra gregaria (Forsk). The penetration oi the sporozoite and its development into a three-segmented cephalont is described. At no time in its development is the Fregarine completely intracellular; the so-called intracellular stages of other workers are shown to be the breakdoan products of the intestinal host cells themselves.
After penetrating the host intestinal cell the sporozoite grows rapidly and the anterior intracellular region outgrows the posterior estracellular region. Once the intracellular region reaches a size 13–16 μ in diameter. growth oi this region ceases and growth is now concentrated in the posterior region. When this latter region has reached 20 μ in diameter an annulus appears. This, by growing diametrically across the posterior epimerite region, divides the extracellular region into protomerite and deutomerite.
Detachment of the cephalont is considered to be a passive and not an active process and is dependent on the breakdown and extrusion of host cells. In this process the epimerite may or may not become detached from the protomerite.
A system of lonpitudinal fibres (myonemes) exists within the protomerite, and these play an important role in converting the protomerite into an adhesil-e disc prior to conjugation.
Extensive folding of the epicyte occurs in both the protomerite and deutomerite in the three-segmented cephalont; this folding could not be observed prior to the division of the gregarine into three regions. The epimerite has a dual function in the early stages of development, serving both as an attachment organelle and as an absorptive region across which iood materials may pass from the host cell.     

Chronologie des Modifications Ultrastructurales au Cours de la Croissance de Gregarina blaberae*

SYNOPSIS. In an ultrastructural study the development of the sporozoite as well as the growth and development of the trophozoite of Gregarina blaberae were followed in the course of experimental infections of larvae of the cockroach Blaberus craniifer. The spectacular growth involved the transformation within 18 days of the sporozoite, measuring 15 × 1 μm, to a cephaline—trophozoite affixed to the intestinal epithelium—of 250 μm length and 65 μm diameter. The sporozoite's ultrastructure is not different from that of sporozoites of other Sporozoa studied to date—the conoid and dense bodies are present. The pellicle consists of 3 membranes, but there are some interruptions in the internal membrane complex. The first dictyosomes are formed from the nuclear envelope. The migration of the nucleus and of the dense bodies, followed by the regression of all the structures characteristic of the sporozoites, and the establishment of a cortical zone that comes to cover the epimerite, take place within 48 hr after infection and mark the transformation of the sporozoite into the trophozoite. Development of the cephaline involves the formation of the epicytic folds, which occurs at the base of the deutomerite, starting on the 3rd day of development. A regular system of longitudinal or epicytic folds is formed over the entire surface of the gregarine. On the 4th and 5th days of development, a vacuolar system and a chondriome become differentiated in the epimerite, while a fibrillar septum separates the protomerite from the deutomerite. The next stage, starting on the 6th day, is characterized by distribution of polysaccharide reserves between these 2 segments. The model studied allows us to determine the role of the epimerite in the parasite's nutrition, as well as the development of the chondriome and of the cortical membranes in the course of the vegetative growth phase of the cephaline gregarine.     

The life cycle of Gregarina ronderosi n. sp. (Apicomplexa: Gregarinidae) in the Argentine grasshopper Dichroplus elongatus (Orthoptera: Acrididae)

Gregarina ronderosi n. sp. is described based on life cycle observations conducted on nymphs and adults of its natural host, the grasshopper Dichroplus elongatus. Following ingestion of oocysts by the host, parasite development occurs between the epithelium and the food mass in the midgut and gastric caeca. Gametocysts are liberated in the faeces. Natural prevalence in the type locality, Girondo, northwestern Buenos Aires Province, was 39.7% (n=131). The earliest trophozoites seen were small (< or = 10 microm), somewhat ovoid, unsegmented bodies. Fully developed trophozoites (the body is divided into epimerite, protomerite, and deutomerite) were slender, with conical or globular epimerites in attached or unattached forms, respectively. Trophozoites varied greatly in size [total length: 10.4-275.1 microm; mean (+/-S.E.): 126.3+/-78.9]. Gamonts, which were the most common stages observed and filled the midgut and gastric caeca in grasshoppers kept in rearing rooms, had a stocky appearance and also varied greatly in size (total length: 80-348 microm; 205+/-13). Association of gamonts was precocious, biassociative, and caudofrontal. Gametocysts were spherical and highly variable in size (96-376 microm in diameter; 202.8+/-52.5), and normally have 14 sporoduct basal discs. Everted sporoducts were up to 60 microm long. Oocysts were uniformly doliform in shape, measured (5+/-0.08 by 3.2+/-0.06 microm) and contained eight sporozoites. Wall reinforcements (carinae) were present. No infection resulted in experimentally inoculated Locusta migratoria, which is a host of Gregarina acridiorum. G. ronderosi is strikingly similar to G. acridiorum, but has larger oocysts.     

Leidyana phryganidiae and Leidyana berkeleyi: Two new species of gregarines from Phryganidia californica

Larvae of the California oakworm, Phryganidia californica, collected in August 1958 in Orcutt, California, were infected by two eugregarines, Leidyana phryganidiae n. sp. and L. berkeleyi n. sp. Both gregarines inhabit the intestine of larvae, and their sporonts are solitary. The maximum length of sporonts of L. phryganidiae is 633 μm; the ratio of length of protomerite to total length (LP:TL) ranges between 1:6.6 and 1:9.6, and the ratio of width of protomerite to width of deutomerite (WP:WD) ranges between 1:1.3 and 1:2.2. The protomerite is conical, longer than wide, and the deutomerite tapers sharply to a point. The maximum length of sporonts of L. berkeleyi is 422 μm; the ratio LP:TL ranges between 1:4.6 and 1:11.2 and WP:WD between 1:0.9 and 1:2.1. The protomerite is hemispherical, and the deutomerite is cylindrical. This is the first record of eugregarine infection in a phytophagous lepidopteran.     

Morphological analysis of the cellular interactions between the eugregarine Gregarina garnhami (Apicomplexa) and the epithelium of its host, the desert locust Schistocerca gregaria

Morphological features of the eugregarine Gregarina garnhami (Canning, 1956) parasitic in the caeca and mid-gut of the desert locust, Schistocerca gregaria, have been studied by transmission and scanning electron microscopy, with particular attention to the epimerite and the relationship between the epimerite and the host epithelium. The cytoplasmic core of the globular epimerite is overlain by a distinct cortical zone, limited on its cytoplasmic face by a membrane-like structure, with an underlying layer of mitochondria. The periphery of the cortical zone is strengthened by a mass of fine filaments, especially at its base. Fine tubular structures, apparently arising from the membrane-like structure, pass through the cortical zone and attach to the epimerite-host cell interface. The base of the cortical zone is supported by a distinct osmiophilic ring. The epimerite is separated from the rest of the gregarine body by a discontinuous septum. Maturing and mature trophozoites possess conically arranged fibrils, which arise from the epimeritic septum and continue into the protomerite region. The epimerite and associated structures are here discussed with regard to the detachment of the trophozoite from the host epithelium. In individuals already detached from the host epithelium, a central depression remained at the top of their protomerite, in the area formerly bearing the epimerite.     

Stylocephalus occidentalis n. sp. (Apicomplexa: Eugregarinida: Stylocephalidae) from Trimytis pruinosa (Coleoptera: Tenebrionidae) in the Nebraska Sandhills

Stylocephalus occidentalis n. sp. (Apicomplexa: Eugregarinida) is described from Trimytis pruinosa (Coleoptera: Tenebrionidae) collected from Keith County in the Sandhills of western Nebraska. Measurements are means in micrometers. Developing trophozoites solitary; epimerite a complex of terminal epimerite and intercalating diamerite; epimerite shallowly ovoid to transversely elliptoid, with transverse basal constriction at junction with diamerite, length 0.5-1 times width, approximately 3-4 times that of diamerite; width approximately equal to that of diamerite; diamerite roughly cylindrical to spindle-shaped, without significant anterior taper, little or no evidence of longitudinal folds, length approximately twice width. Association late, frontal, isogamontic. Gamont protomerite depressed ovoid to very broadly ovoid, length 27.3, width 35.1, anterior distance to widest point 15.4. Protomerite-deutomerite septum clearly marked and constricted, width 34.6. Deutomerite often with distinct marginal crenulation, narrowly obovoid to very narrowly obovoid, length 356.5, maximum width 57.6, anterior distance to widest point 26.3, equatorial width 35.1, +/-12.5, 29. Total length 381.5. Nucleus ellipsoid, length 32.5, width 18.8; with 0 or 2 polysomal endosomes. Gametocysts roughly spherical; diameter 205.0; wall desiccating to become paper-like, slightly papillated, dehiscing by simple rupture, releasing oocysts in coiled chains, epispore packet absent, gametocyst residuum present. Oocysts dark brown to black, axially asymmetric, broadly deltoid, gibbous in lateral aspect, slightly keeled in dorsal aspect; length 9.8, height 7.9; with slight terminal protuberances and 2 central, spherical residua.     

Ultrastructure de la Grégarine Callynthrochlamys phronimae Frenzel; Étude Comparée de son Noyau avec Celui de Thalicola salpae (Frenzel) (Eugregarina)

SYNOPSIS. The structure of the gregarine Callynthrochlamys phronimae has been studied with the electron microscope. The cuticular complex is not different from those previously described in other species of gregarines. It is composed of 2 layers of different thickness delimited by 3 unit membranes and constitutes series of oblique folds at the surface of the deutomerite. Longitudinal rods of dense material surrounded by a slight pellicle are seen under the cuticle. Pinocytic vacuoles are present under the surface of the gregarine. Cytoplasmic organelles include mitochondria, Golgi complexes, endoplasmic reticulum, vacuoles and dense bodies from different sizes. There is a connection between the different features of the cytoplasm in the protomerite and deutomerite and the corresponding cuticular organization.
A characteristic feature of the species is the peculiar differentiation of the nuclear membrane. The nucleus is surrounded by a typical double membrane of which the inner one has a dense fibrillar layer apposed to it. In mature trophozoites, tubular expansions without inner layer arise from the double membrane; the same type of nuclear membrane occurs in another species, Thalicola salpae.     

Insecticidal action of Bauhinia monandra leaf lectin (BmoLL) against Anagasta kuehniella (Lepidoptera: Pyralidae), Zabrotes subfasciatus and Callosobruchus maculatus (Coleoptera: Bruchidae)

Bruchid beetle larvae cause major losses in grain legume crops throughout the world. Some bruchid species, such as the cowpea weevil (Callosobruchus maculatus) and the Mexican bean weevil (Zabrotes subfasciatus), are pests that damage stored seeds. The Mediterranean flour moth (Anagasta kuehniella) is of major economic importance as a flour and grain feeder; it is often a severe pest in flour mills. Plant lectins have been implicated as antibiosis factors against insects. Bauhinia monandra leaf lectin (BmoLL) was tested for anti-insect activity against C. maculatus, Z. subfasciatus and A. kuehniella larvae. BmoLL produced ca. 50% mortality to Z. subfaciatus and C. maculatus when incorporated into an artificial diet at a level of 0.5% and 0.3% (w/w), respectively. BmooLL up to 1% did not significantly decrease the survival of A. kuehniella larvae, but produced a decrease of 40% in weight. Affinity chromatography showed that BmoLL bound to midgut proteins of the insect C. maculatus. 33 kDa subunit BmoLL was not digested by midgut preparations of these bruchids. BmoLL-fed C. maculatus larvae increased the digestion of potato starch by 25% compared with the control. The transformation of the genes coding for this lectin could be useful in the development of insect resistance in important agricultural crops.     

Effect of diet and mating status on ovarian development and oviposition in the polyphagous predator Macrolophus caliginosus (Heteroptera: Miridae)

The mirid bug Macrolophus caliginosus is commercially reared on eggs of Ephestia kuehniella, constituting an effective but expensive factitious food. Artificial diets can decrease the rearing costs of this natural enemy, but developing and evaluating an artificial diet is a very time-consuming activity. In the current study, development and reproduction of M. caliginosus on two artificial diets based on egg yolk were investigated. The artificial diets resulted in longer development and lower adult weights, but survival was comparable with that of control insects fed E. kuehniella eggs. Reproductive potential of the predator reared on factitious and artificial foods was assessed using a dissection method. The influence of nymphal food on fecundity was less important than that of adult food. Adults fed E. kuehniella eggs had a preoviposition period of about 4 days, whereas adults offered only plant material started laying eggs about 7 days after emergence. Ovarian scores at day 7 were higher for females fed E. kuehniella eggs than for those given access only to a tobacco leaf. Ovarian scores were not significantly affected by mating status. In a final test, a parallel comparison of two methods for assessing reproductive response to diet was made. Here, adult couples were offered one of four diets: E. kuehniella eggs, one of two artificial diets or no food. Half of the females were dissected and the other half was held for determining lifetime oviposition. Females fed E. kuehniella eggs had superior ovarian scores and laid more eggs than those fed either artificial diet or those given no extra food. A good correlation (r = 0.97) was obtained between ovarian scores and oviposition data, indicating that dissecting females after 1 week provides a reliable estimate of fecundity as affected by diet quality. Rapid reproductive assessments as used in the current study will help to increase the rate of development of artificial diets and may contribute to more cost effective production methods for augmentative biological control agents.     

Chronology of the ultrastructural modifications during the growth of Gregarina blaberae]

In an ultrastructural study the development of the sporozoite as well as the growth and development of the trophozoite of Gregarina blaberae were followed in the course of experimental infections of larvae of the cokroach Blaberus craniifer. The spectacular growth involved the transformation within 18 days of the sporozoite, measuring 15 X 1 micronm, to a cephaline--trophozoite affixed to the intestinal epithelium--of 250 micronm length and 65 micronm diameter. The sporozoite's ultrastructure is not different from that of sporozoites of other Sporozoa studies to date--the conoid and dense bodies are present. The pellicle consists of 3 membranes, but there are some interruptions in the internal membrane complex. The first dictyosomes are formed from the nuclear envelope. The migration of the nucleus and of the dense bodies, followed by the regression of all the structures characteristic of the sporozoites, and the establishment of a cortical zone that comes to cover the epimerite, take place within 48 h after infection and mark the transformation of the sporozoite into the trophozoite. Development of the cephaline involves the formation of the epicytic folds, which occurs at the base of the deutomerite, starting on the 3rd day of development. A regular system of longitudinal or epicytic folds is formed over the entire surface of the gregarine. On the 4th and 5th days of development, a vacuolar system and a chondriome become differentiated in the epimerite, while a fibrillar septum separates the protomerite from the deutomerite. The next stage, starting on the 6th day, is characterized by distribution of polysaccharide reserves between these 2 segments. The model studied allows us to determine the role of the epimerite in the parasite's nutrition, as well as the development of the chondriome and of the cortical membranes in the course of the vegetative growth phase of the cephaline gregarine.     

The Ultra‐Structural Similarities between Cryptosporidium parvum and the Gregarines

Using a transmission electron microscopy‐based approach, this study details the striking similarities between Cryptosporidium parvum and the gregarines during in vitro axenic development at high ultra‐structural resolution. C. parvum zoites displayed three unusual regions within uninucleated parasites: epimerite‐like, protomerite‐like, and the cell body; these regions exhibited a high degree of morphological similarity to gregarine‐like trophozoites. The presence of a mucron‐like bulging structure at the side of the free ovoid gregarine‐like zoites was observed after 2 h of cultivation. An irregular pattern of epicytic‐like folds were found to cover the surface of the parasites 24 h postcultivation. Some extracellular stages were paired in laterocaudal or side‐side syzygy, with the presence of a fusion zone between some of these zoites. The present findings are in agreement with phylogenetic studies that have proposed a sister relationship with gregarines. Cryptosporidium appears to exhibit tremendous variety in cell structure depending on the surrounding environment, thereby mimicking the “primitive” gregarines in terms of the co‐evolution strategy between the parasites and their environments. Given this degree of similarity, different aspects of the evolutionary biology of Cryptosporidium need to be examined, considering the knowledge gained from the study of gregarines.     

Epimerite-host epithelium relationships among eugregarines parasitizing the damselflies Enallagma civile and Ischnura verticalis.

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.     

Myosin-Like Protein (MR 175,000) In Gregarina Blaberae

ABSTRACT. A myosin-like protein (M_r 175,000) was detected in the parasitic protozoan Gregarina blaberae , by both immunofluorescence and immunoblotting of one- and two-dimensional electrophoresis gels using anti-myosin antibodies. This protein was present in the trophozoite ghost but not in the cytoplasmic extract, nor in extract from the sexual stage, suggesting a protein-stage-dependent expression. the protein tightly bound to the cortical membranes was insoluble at low ionic strength, or in detergent solutions, but could be extracted from Gregarina ghosts by 6 M urea in high ionic strength solution (0.5 M NaCI) and in the presence of reducing agents (20 mM DTT). the protein was localized by indirect immunofluorescence in the cortex of the epimerite, in the fibrillar disc (the socalled septum) separating the proto- and the deutomerite segments, in the contractile ring or sphincter at the top of the protomerite, and as longitudinal lines underlying the G. blaberae epicyte folds. the presence of both actin-like and myosin-like proteins would be consistent with a role in gliding and other cell motility processes of this parasite.     

Naiadocystis phykoterion n. gen., n. sp. (Apicomplexa: Eugregarinida: Hirmocystidae), from the Mexican pygmy grasshopper, Paratettix mexicanus (Orthoptera: Tetrigidae), in the Texas big thicket with recognition of three previously described species of Naiadocystis

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 degrees, 150 degrees, 210 degrees, and 330 degrees, 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).     

Determination of Homalodisca coagulata (Hemiptera: Cicadellidae) egg ages suitable for oviposition by Gonatocerus ashmeadi, Gonatocerus triguttatus, and Gonatocerus fasciatus (Hymenoptera: Mymaridae)

Homalodisca coagulata (Say) (Hemiptera: Cicadellidae) eggs 1–10 days of age were exposed to Gonatocerus ashmeadi Girault, Gonatocerus triguttatus Girault, and Gonatocerus fasciatus Girault (all Hymenoptera: Mymaridae) in no choice laboratory trials to investigate egg age utilization and to determine which egg ages are vulnerable to attack by these three parasitoids. The H. coagulata egg ages that were most suitable for oviposition by G. ashmeadi, G. triguttatus, and G. fasciatus were eggs 3, 4, and 2 days of age, respectively. Egg ages least suitable for parasitoid development were 6–10 days for G. ashmeadi (resulting in <50% parasitism), 1–2 and 7–10 days for G. triguttatus (resulting in <25% parasitism), and 3–10 days for G. fasciatus (resulting in <11% parasitism). Pooling parasitism data across all egg ages showed that parasitism by G. ashmeadi was 12.9 and 28.5% higher compared with G. triguttatus and G. fasciatus, respectively, and G. triguttatus resulted in 15.6% higher percentage parasitism compared with G. fasciatus. Egg age had a significant effect on the percentage of female G. ashmeadi offspring produced, but this was not significant for G. triguttatus, and low G. fasciatus parasitism prevented statistical analyses for comparisons. Results from tests where females were offered a choice for oviposition between eggs 1, 3, and 5 days of age demonstrated that G. ashmeadi and G. triguttatus showed no significant oviposition preference, while percentage parasitism by G. fasciatus was 29.4 and 7.4% higher when females were presented eggs 1 and 3 days of age, respectively, compared with eggs 5 days of age. Choice tests indicated that an overlap in egg age suitability for oviposition exists between G. ashmeadi, G. triguttatus, and G. fasciatus, and that interspecific competition for eggs 1, 2, and 3 days of age may occur in the field environment.