The sexual adult of Cercaria praecox Walker, 1971 (Digenea: Fellodistomidae), with the proposal of Oceroma n. g.

A sexual adult trematode that is considered to be conspecific with the distinctive larval trematode Cercaria praecox Walker, 1971 is reported from the kyphosid fish Scorpis lineolata Kner in Moreton Bay, Queensland, Australia. The sexual adult is consistent with the cercarial body of Cercaria praecox in having a single caecum with an asymmetrical appendix, symmetrical testes immediately posterior to the ventral sucker, and the ovary and vitellarium both well posterior to the testes. This combination of characters is distinct within the Fellodistomidae Nicoll, 1909 and requires the proposal of a new genus, Oceroma n. g. Analysis of 28S rDNA sequences demonstrates that this species forms a clade with Coomera Dove & Cribb, 1995 within the Fellodistomidae. The life-cycle of the species is predicted to require two hosts and to involve the direct ingestion of the cercaria.     

Studies on Cercariae from Kuwait Bay. XI. Description and surface topography of Cercaria kuwaitae XI sp.n. (Digenea: Echinostomatidae)

A new echinostome cercaria, Cercaria kuwaitae XI sp.n., from the prosobranch gastropod Cerithidea cingulata (Gmelin) from Kuwait Bay is described. The new cercaria is characterized by 23 collar spines and primary excretory tubules with distinct diverticula. The cercaria encysts in the snail host and is similar to those of Acanthoparyphium sp. The surface topography of the redia, cercaria and metacercarial cyst wall is studied by scanning electron microscopy. This is the first echinostome cercaria to be recorded in a gastropod from the Arabian Gulf region.     

Some results of the study of trematode fauna of the freshwater mollusc Melanopsis praemorsa (L.) from Azerbaijan water bodies. Report 3. New species of stylet cercaria

The structure (illustrated by pictures) and differential diagnoses of 3 new closely related forms of stylet cercaria (Cercaria agstaphensis 8, Cercaria agstaphensis 21 and Cercaria agstaphensis 16) are given. Special attention was paid to the armament of the glandular apparatus, to the excretory and digestive systems, and to other taxonomically important structural peculiarities.     

Cercaria caribbea LVIII Cable, 1963 (Digenea: Cyathocotylidae) in the Republic of Korea and its surface ultrastructure

Cercaria caribbea LVIII Cable, 1963 (Digenea: Cyathocotylidae) was detected from a brackish water gastropod species (Cerithideopsilla cingulata) in a coatal area of Shinan-gun, Jeollanam-do (Province), the Republic of Korea, and its surface ultrastructure was studied using a scanning electron microscope. The cercariae were found freely swimming or enveloped within daughter sporocysts when the snail host was mechanically broken. They were morphologically characterized by a linguiform and ventrally concave body, a long and bifurcated tail, and the presence of a holdfast (=tribocytic) organ posterior to the ventral sucker. On the whole ventral and dorsal surfaces, peg-like tegumental spines were densely distributed. Around the oral sucker, several sensory papillae, each with a short cilium, were distributed, and on the tail, sensory papillae, each with an extensively long cilium, were observed. This is the first record describing a cyathocotylid cercaria from a brackish water gastropod in the Republic of Korea.     

Cercaria splendens Szidat--larva of the trematode Azygia lucii Looss]

The belonging of the only one "gigantic cercaria", Cercaria splendens, to the species Azygia lucii was proved experimentally. The geographic distribution of A. lucii is considerably wider than it has been indicated up to now. The distribution area of A. robusta is also confined not only to the Asiatic part of the USSR. The following characters are suggested for distinguishing the Azygia species: the shape and size of the pharynx, the spread of vitellaria beyond the posterior border of the testes and ratio between the sizes of suckers.     

A review of the currently recognised opecoelid cercariae,including the identification and emergence ecology of Cercaria capricornia XII (Digenea: Opecoelidae) from Nassarius olivaceus (Gastropoda: Nassariidae) in Central Queensland,Australia

A new opecoelid cercaria, Cercaria capricornia XII, is reported from Nassarius olivaceus in Capricornia, Central Queensland, Australia. Combined molecular and morphological data indicate that this cercaria is a member of the subfamily Opecoelinae. Cercaria capricornia XII is the first known opecoeline cercaria reported from a nassariid gastropod. Cercaria capricornia XII can be distinguished from other opecoelid cercariae by the combination of the presence of a 2-pointed stylet, body length and width, and the size of the tail. The emergence pattern for C. capricornia XII in captivity was erratic; rapid emergences of thousands of cercariae were interspersed by periods that sometimes exceeded a month in which no emergence occurred. There was no detectable pattern to or stimulus of the emergence. The molluscan host range of opecoelids is analysed in detail. Gastropods from the Buccinoidea, Cerithioidea and Rissooidea are hosts to both opecoeline and plagioporine cercariae, but the dominant subfamily infecting the Cerithioidea and Rissooidea is the Plagioporinae. The dominant marine host gastropod superfamily for opecoeline cercariae is the Buccinoidea; the family Nassariidae is contained in the Buccinoidea. The range of gastropod superfamilies known as hosts of plagioporines is much broader than that for opecoelines, which may be explained by the relative size of the two opecoelid families and perhaps by indications that the Plagioporinae is polyphyletic.     

长尾蚴吸虫幼虫在菲律宾蛤仔的寄生部位及其组织化学的研究

本文报道长尾蚴吸虫幼虫在菲律宾蛤仔的寄生部位及其组织化学的研究,长尾蚴吸虫幼虫主要寄生于哈仔的生殖腺组织中,仅少部分进入生殖腺附近的消化腺,鳃等。受感染严重的蛤仔,其生殖腺的滤泡等组织被虫体占满并被耗尽,长尾蚴吸虫子胞蚴的胞壁及尾蚴的皮导主要含碱性蛋白质和粘蛋白,子胞蚴的胚球,尾蚴的吸盘,生殖原基,单细胞腺体主要ＤＮＡ阳性物质,排泄囊含丰富的碱性蛋白质;尾蚴体的中部含有呈颗粒团的粘蛋白和抗淀粉酶的     

A histochemical study of the secretory gland cells of Cercaria shikokuensis and their role during development from cercaria to metacercaria.

The roles of secretory glands during the developmental process from an immature cercaria to a metacercaria in Cercaria shikokuensis were studied. Four types of secretory cells were identified in this species. On maturation of the cercaria in redia, the products of ventral gland cells and mucoid gland cells formed a thick surface coat on the mature cercaria, and the products of cephalic gland cells also formed a thin cover on the surface coat. In the process leading to the formation of a metacercaria, the surface coat constituted the outer layer of the cyst, mucoid gland cells secreted mucous substances inside the wall, and then cystogenous gland cells discharged their products to the inner wall. The cyst wall was composed of four layers, and it was thought that the outermost surface layer helped the cyst wall to adhere to the matrix and the intermediate layers helped to put together outer and inner walls.     

Cercaria orospinosa Encountered in the Snail Melanopsis praemorsa L. from a Mountain Stream in Turkey

Cercaria orospinosa is the only cercaria shed by Melanopsis praemorsa snails in Savanda stream, Turkey. Magnitude of infestation of snails by this cercaria was correlated with size of the snails and strength of the water current. The highest degree of infestation occurred in June, while in winter it was reduced to zero. The cercariae were released from rediae, which were found in the hepatopancreas of the snails.     

Cercaria sevillana n sp,a new cercaria (Digenea: Microphallidae) from Nassarius reticulatus (L) (Mollusca: Prosobranchia) in Portugal

Cercaria sevillana n. sp. (Digenea: Microphallidae) was discovered infecting the gonads and digestive gland of the prosobranch Nassarius reticulatus (L.) (Nassariidae) collected from the Ria de Aveiro, Portugal. Cercariae were obtained by natural emission and were studied under a differential interference contrast microscope and scanning electron microscope (SEM). C. sevillana n. sp. is identical to the cercaria found by Dolgikh (1965) in the same mollusc host from the Black Sea, but erroneously named C. misenensis Palombi, 1940, which is a parasite of Cerithium rupestre Risso, 1826 (Cerithiidae). Cercaria sevillana n. sp. can be distinguished from C. misenensis by its tail being shorter than the cercarial body, as well as by differences in the pattern of penetration glands the size and shape of the stylet and excretory vesicle, and its behavioural pattern. An unusual structure of the tail of this new cercaria was observed by SEM; it is characterised by the presence of annular folded membranes arranged as overlapping flounces around its central axis. This resembles the traditional skirts of the women of Seville. Such a morphological feature of the tail has not been previously observed, but may be a feature of many microphallid cercariae.     

Clarification of Cercaria sevillana (Digenea: Microphallidae) life cycle using morphological and molecular data

Cercaria sevillana is the cercaria larval stage that infects the gonads and the digestive gland of its first intermediate host, Nassarius reticulatus. In this study the decapodous crustacean Carcinus maenas was used to determine if it would serve as second intermediate host in the parasite's life cycle. The latter hypothesis was based on the knowledge that C. maenas is the second intermediate host of several other digenean species. After dissection, it was possible to observe encysted metacercariae in the antennal glands of the green crab. After biochemical excystment, the metacercariae were processed for light and scanning electron microscopy. The morphological features observed led us to conclude that this species was a microphallid fluke, and it was identified as Gynaecotyla longiintestinata. To establish a possible relationship between C. sevillana and this metacercariae, the ITS1 region was analyzed. Thus, DNA was extracted from C. sevillana and from the cysts isolated from the antennal glands. The ITS1 region was amplified and sequenced, and the alignment clearly demonstrated that the cercaria and the metacercariae belonged to the same species, G. longiintestinata.     

Experimental research on the biological cycle of Phyllodistomum elongatum Nybelin, 1926 (Digenea: Gorgoderidae Looss, 1901)]

Experimental infection of Tinca tinca and Carassius auratus have demonstrated that Cercaria duplicata von Baer, 1827 is the larval form of Phyllodistomum elongatum Nybelin, 1926 and that the life-cycle occurs between Anodonta cygnea (intermediate host) and Tinca tinca or Carassius auratus (final host) without a second intermediate host. The life-history experimentally completed in the laboratory occurs in the following way: -- adult in the ureters of Tinca tinca and Carassius auratus; -- mother sporocyst and daughter sporocyst of Phyllodistorum elongatum in Anodonta cygnea give rise to the large-tailed rhopalocercous cercaria; -- metacercaria encysted within transformed tail in water.     

Effects of trematode double infection on the shell size and distribution of snail hosts

Infection with larval trematodes sometimes alters the phenotypes of their snail hosts. While some trematode species have distinct effects on host phenotypes, it is still unclear how snail phenotypes are altered when they are parasitized with multiple trematode species. Here, we report that double infection with trematode species averages the effects of parasitic alteration on host phenotype. We found that snail hosts Batillaria attramentaria (Batillariidae) infected with Cercaria batillariae (Heterophyidae) have abnormally large shells and distribute in lower areas of the intertidal zone. Snails with another dominant trematode species, the renicolid cercaria I (Renicolidae), have slightly larger shells and distribute in upper areas of the intertidal zone. A number of double infections with both trematodes was observed in this study. Snails infected with both trematode species exhibited an intermediate size and inhabited a depth between those of snails solely infected with either trematode species, suggesting that the two trematodes simultaneously affected the snail phenotypes. Because altered host phenotypes are frequently beneficial to parasites, two trematode species may compete for successful transmission through alteration of host phenotypes.     

The effect of different temperatures on the development of intra-molluscan stages of

The duration of various development stages of inside the intermediate host were determined at different constant temperatures ranged from 12° to 30°C. The rate of development of sporocyst, redia, daughter redia and cercaria was accelerated as a result of increasing the temperature. Thus, an increase in the incubation temperatures from 15° to 30°C reduced the duration of sporocyst from 21 to 4 days, the redia from 37 to 11 days, daughter redia from 53 to 22 days and the cercaria from 73 to 25 days. At 12°C, the parasite developed to redial stage only and it required 51 days. Cercaria formation was observed at temperatures between 15 to 30°C. The highest cercaria output/snail was observed at 15°C and the lowest at 30°C.     

Some aspects of the biology of the cercaria and metacercaria of Stephanostomum baccatum (Nicoll, 1907) Manter, 1934 (Digenea: Acanthocolpidae)

Experimental proof is presented that Cercaria neptunae Lebour is the cercaria of Stephanostomum baccatum and that the gastropods Buccinum undatum (L.) and Neptunea antiqua (L.) both act as its first intermediate hosts in the north-east Atlantic. Heavy experimental infections were associated with mortalities of 0+plaice Pleuronectes platessa (L.). The probable effects on plaice of infections at intensities below the lethal level are discussed. Under natural conditions almost all S. baccatum infection of plaice occurs in the first year of life, but newly emerged cercariae were shown experimentally to be capable of encysting in the musculature of plaice up to three years old. The thicker epidermis of older plaice may account for their resistance to infection. Common dabs were more easily infected than plaice. The ability of S. baccatum cercariae to infect plaice and common dabs is inversely related to the length of time between emergence and contact with the host. The differences in skin structure between opposite sides of the plaice body may account for the asymmetrical distribution of metacercariae in the musculature. The potential use of S. baccatum as a biological tag is discussed.     

A new acanthocolpid cercaria (Digenea) from Cantharus dorbignyi (Prosobranchia) in the Western Mediterranean

A new cercaria is recorded from the prosobranch snail Cantharus dorbignyi from the sublittoral region off the coast of Corsica. The redia, cercaria and metacercaria (the latter experimentally developed in the labrid fishes Symphodus ocellatus and S. rostratus) are described, along with the behaviour of naturally emitted cercariae. In view of the morphology of the larval stages, the parasite is thought likely to be an acanthocolpid. The morphology of the cercaria and metacercaria are compared with both known and suspected acanthocolpid cercariae and with adult acanthocolpids known to occur in the Mediterranean. Morphological and circumstantial evidence suggests that this cercaria may be a species of the genus Tormopsolus.     

The effect of different temperatures on the development of intra-molluscan stages of Fasciola gigantica

The duration of various development stages of $\text{Fasciola gigantica}$ inside the intermediate host $\text{Lymnaea auricularia}$ were determined at different constant temperatures ranged from 12° to 30°C. The rate of development of sporocyst, redia, daughter redia and cercaria was accelerated as a result of increasing the temperature. Thus, an increase in the incubation temperatures from 15° to 30°C reduced the duration of sporocyst from 21 to 4 days, the redia from 37 to 11 days, daughter redia from 53 to 22 days and the cercaria from 73 to 25 days. At 12°C, the parasite developed to redial stage only and it required 51 days. Cercaria formation was observed at temperatures between 15 to 30°C. The highest cercaria output/snail was observed at 15°C and the lowest at 30°C.