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Morphology of Bertiella studeri (Blanchard, 1891) sensu Stunkard (1940) (Cestoda: Anoplocephalidae) of human origin and a proposal of criteria for the specific diagnosis of bertiellosis.

Human material of an African specimen of Bertiella studeri (Blanchard, 1891), a typical intestinal cestode of monkeys, is described. Mature, postmature and gravid proglottides, and eggs, previously inadequately figured, are illustrated and photographed. The description of the species agrees with that provided by Stunkard (1940). A comparative study with other descriptions of the species is made in an attempt to clarify previous findings. The morphological differences reported in various earlier descriptions of the species suggest that B. studeri should be regarded as a "B. studeri species complex" Improvements are required in the descriptions of new future findings in order to clarify the specific diagnosis of human bertiellosis. Evidence suggests that a generalised diagnosis exclusively based on egg size and geographical distribution is insufficient to differentiate B. studeiri and Bertiella mucronata (Meyner, 1895), or additional species may be affecting humans.

Animals↗

Ultrastructure of the scolex, rhyncheal system and bothridial pits of Otobothrium mugilis (Cestoda: Trypanorhyncha).

The ultrastructure of the scolex tegument, bothridial pits (=ciliated pits) and rhyncheal system of Otobothrium mugilis Hiscock, 1954 is described from plerocerci collected from the teleosts Arius graeffei Kner et Steindachner and Mugil cephalus Linnaeus. Scanning electron microscopy revealed that filamentous microtriches with shortened caps are abundant across the entire surface of the tegument. Palmate microtriches are dominant on the bothridia and their margins. The surfaces of bothridial pits were covered with large bifid microtriches. The bothridial pits are strongly muscularised invaginations of the tegument. Nervous tissues were not observed within the pits and it is probable that these structures function as accessory attachment structures. The wall of each tentacle sheath consists of one to three bands of fibrils, lined internally by a thin cytoplasmic layer. The tentacular walls are cellular, containing myofilaments. The fibrils of the tentacular walls are arranged into discrete blocks of parallel fibrils and appear to be intracellular. Tentacular walls are lined externally by a modified membrane with an external glycocalyx. Tentacular hooks are solid, bound externally by a membrane. The body of the hook contains numerous longitudinal canaliculi and an electron-opaque medulla lies at the centre of the hook.

Animals↗

Chimaerula bonai sp. n. (Cestoda: Dilepididae) from the bare-faced ibis, Phimosus infuscatus (Lichtenstein) (Aves: Threskiornithidae) in Paraguay.

Chimaerula bonai sp. n. is described from the small intestine of Phimosus infuscatus (Lichtenstein) in Paraguay. The new species differs from the other two species of Chimaerula Bona, 1994, i.e., Chinmaerula woodlandi (Prudhoe, 1960) and Chinmaerula leonovi (Belogurov et Zueva, 1968), mainly by the intermediate number of rostellar hooks (30-34 compared to 42-46 in the former and 20-22 in the latter), longer rostellar hooks (31-34 microm versus 26 microm and 19-21 microm, respectively), shorter cirrus sac (58-82 microm versus 158-201 microm and 134-183 microm, respectively) and the absence of rosethorn spines in the cirrus armament. Modifications in the generic diagnosis of Chimaerula are proposed in order to conform it with some peculiarities of the new species (i.e., the relatively small and thin cirrus, the absence of rosethorn spines in its armament and the small cirrus sac).

Animals↗

Grillotia borealis sp. n. (Cestoda: Trypanorhyncha) from five species of Bathyraja (Rajiformes: Arhynchobatidae) in the North Pacific Ocean with comments on parasite enteric distribution.

A new trypanorhynch cestode, Grillotia borealis sp. n., is described from the spiral intestines of softnose skates of the genus Bathyraja collected from subarctic waters of the North Pacific Ocean: B. parmifera (Bean) (type host), B. aleutica (Gilbert) and B. interrupta (Gill et Townsend) from the Bering Sea and B. minispinosa Ishiyama et Ishihara and B. sminovi (Soldatov et Pavlenko) from the Sea of Okhotsk off Japan. The new species is distinguished from other species of Grillotia by possession of the following combination of characters: four hooks per principal row, hooks 4(4') distinctly separated from hooks 3(3') of principal row, principal rows separated by 13-15 intercalary hooks in 2-3 rows, hooks 2(2') and 3(3') change in form along their respective files, hooks 1(1') do not change in form along the file, a broad band of microhooks on the external tentacular face, intermediary hooks are lacking, absence of a special basal armature, origin of the retractor muscle near middle of the bulb, average scolex ratio of 1:3:2:0.1, and a hermaphroditic sac. Grillotia borealis consistently favoured the most anterior regions of the spiral intestine. Seventy-one per cent of 21 attached worms occupied the most anterior chamber of the spiral valve and 52 per cent were embedded in the anterior surface of the spiral valve whorls. Factors which may limit the distribution of G. borealis within the spiral intestine of its host are discussed. Statistically significant differences occur in the mucosal morphology of B. aleutica and B. parmifera for villus length, diameter, spatial arrangement and number per unit area along the antero-posterior axis of the spiral intestine.

Animals↗