The life-cycle of Bucephaloides gracilescens (Rudolphi, 1819) Hopkins, 1954 (Digenea: Gasterostomata)

Parasitology ◽  
1974 ◽  
Vol 68 (1) ◽  
pp. 1-12 ◽  
Author(s):  
R. A. Matthews

The cercaria and sporocyst of Bucephaloides gracilescens are described from Abra alba (Wood). Observations were made on the behaviour of the cercaria and the mechanism of release from the first intermediate host. The metacercaria was obtained experimentally for the first time using Ciliata mustela (L.), a species of Gadidae from rock pools, as second intermediate host. It has not previously been recorded from this fish. Unsuccessful attempts were made to infect species of fishes from three other families, namely, Bothidae, Pleuronectidae and Gobiidae, confirming the high degree of host specificity of the metacercaria to Gadidae. The metacercaria, its development and effect on the host are briefly discussed. It was linked with the adult on the basis of comparative morphology and ecology of the hosts.

1992 ◽  
Vol 66 (1) ◽  
pp. 53-61 ◽  
Author(s):  
K. Ando ◽  
H. Tokura ◽  
H. Matsuoka ◽  
D. Taylor ◽  
Y. Chinzei

ABSTRACTThe life cycle of Gnathostoma nipponicum was examined by field survey and by experimental infection of animals with the larvae. Naturally infected larval G. nipponicum were found in loaches, catfish, and snakes. Experimentally, loaches, killifishes, frogs, salamanders, mice, and rats were successfully infected with the early third-stage larvae of G. nipponicum obtained from copepods (the first intermediate host), whereas snakes, quails, and weasels were not. Frogs, snakes, quails, and rats were experimentally infected with the advanced third-stage larvae (AdL3) from loaches. These results reveal that some species of fishes, amphibians and mammals can act as the second intermediate host and that some species of reptiles, birds and mammals can act as a paratenic host. The life cycle was completed in weasels, the definitive host, which were infected with AdL3 from loaches and started to evacuate eggs of G. nipponicum in faeces on days 65–90 postinfection.


1944 ◽  
Vol 22d (1) ◽  
pp. 6-16 ◽  
Author(s):  
Thomas W. M. Cameron

A trematode, widely distributed in Canada, and occurring in man and other fish-eating mammals, is described and its taxonomy discussed. Its life cycle has been worked out and it is shown to involve a snail, Amnicola limosa porata as first intermediate host and a fish, the common sucker (Catostomus commersonii) as the second intermediate host. The larval stages are described.


1999 ◽  
Vol 73 (2) ◽  
pp. 103-113 ◽  
Author(s):  
H.E.M. El-Darsh ◽  
P.J. Whitfield

A detailed examination of the abundant flatfish speciesPlatichthys flesus, the flounder, in the tidal Thames has revealed the presence of four digenean metacercarial parasites,Cryptocotyle concava(Creplin, 1825),Timoniella imbutiforme(Molin, 1859),T. praeterita(Looss, 1901) andLabratrema minimus(Stossich, 1887). Flounders were recorded as a new second intermediate host forT. praeteritaandL. minimus. They were also recorded as second intermediate hosts for the first time in British waters forT. imbutiforme. The temporal and spatial characteristics of these infections were examined and were believed to provide indirect parasitological evidence of the movement patterns of flounders during their utilization of the Thames Estuary as a nursery ground. From these data it was also surmised that the first intermediate host ofT. imbutiforme,T. praeteritaandC. concavawas probably the molluscan speciesHydrobia ulvaein the lower Thames Estuary, whereasL. minimuswas most likely to occur in the molluscan hostCerastoderma edule, also present in the lower estuary.


1985 ◽  
Vol 33 (5) ◽  
pp. 715 ◽  
Author(s):  
TH Cribb

Opecoelus variabilis, sp. nov., is described from the intestine of 17 species of Australian freshwater fish. The highly variable anatomy of this species highlights the closeness of Opecoelus and Opegaster. Opegaster is made a synonym of Opecoelus and a new diagnosis is proposed for Opecoelus. The first intermediate host of O. variabilis is the prosobranch snail Posticobia brazieri, and the second intermediate hosts are five species of atyid, palaemonid and parastacid Crustacea. Features of the life cycle are the production of daughter sporocysts by the mother sporocyst when only one-quarter of its full size, and the further development of the metacercaria in the second intermediate host after becoming infective to the definitive host.


Author(s):  
Miriam Rothschild

If the number of infections with (a) trematode parthenitae and cercariae using Littorina neritoides as first intermediate host only, and (b) encysted metacercariae using L. neritoides as second intermediate host only, are plotted against the size of the snails, two different curves result. The first shows a low rate of infection in the small size groups, but a steep upward slope rising to 91% in the large size groups. The second shows a curve increasing uniformly to 87% infection.Possible interpretations are discussed, and it is concluded that the difference is probably due to the fact that primary infections cause accelerated growth in the host.


1987 ◽  
Vol 65 (10) ◽  
pp. 2491-2497 ◽  
Author(s):  
Murray J. Kennedy ◽  
L. M. Killick ◽  
M. Beverley-Burton

Life cycle studies of Paradistomum geckonum (Dicrocoeliidae) were attempted experimentally. The pulmonate gastropod Lamellaxis gracilis served as the first intermediate host; geckonid lizards (Cosymbotus platyurus, Gehyra mutilata, and Hemidactylus frenatus) served as definitive hosts. The life cycle of Mesocoelium sociale (Mesocoeliidae) was studied in naturally infected first intermediate hosts (L. gracilis, Huttonella bicolor) and experimentally in geckonid definitive hosts (C. platyurus, G. mutilata, and H. frenatus). Some naturally infected L. gracilis were infected concurrently with larval stages of both digeneans. Second intermediate hosts, presumed to be arthropods, were experimentally unnecessary. Metacercariae of P. geckonum were not found. Cercariae of M. sociale formed encysted metacercariae in the same individual snails.


1972 ◽  
Vol 46 (2) ◽  
pp. 125-137 ◽  
Author(s):  
R. C. Chhabra ◽  
Kunwar Suresh Singh

The development of the preinfective stages of S. lupi has been described and illustrated and the details of morphology given for the first time.The sex of the first stage juveniles can be distinguished by locating the position of the genital primordium. On an average, the first stage juveniles measure 0·39 mm. in length and 0·036 mm. in breadth, early second stage 0·78 and 0·044 mm. and the advanced second stage 1·40 mm. and 0·63 mm. respectively. The second stage juveniles obtained from beetles were not infective to dogs.


2020 ◽  
Vol 94 ◽  
Author(s):  
D. Krupenko ◽  
A. Uryadova ◽  
A. Gonchar ◽  
G. Kremnev ◽  
V. Krapivin

Abstract Few digeneans of the family Fellodistomidae are known from the Russian Arctic seas. The taxonomic status of these species, their life cycles and host range raised recurrent questions, some of which remain unanswered. To revise the species composition and life cycles of fellodistomids in the White Sea, we searched for them in several known and suspected hosts: wolffish, flatfishes (definitive), gastropods of the family Buccinidae (second intermediate) and protobranch bivalves (first intermediate). Species identification was based both on morphology and 28S ribosomal RNA gene sequences. We found Fellodistomum agnotum in the White Sea for the first time. Buccinum undatum was proved to be intermediate host of both F. agnotum and Fellodistomum fellis, and metacercariae of F. fellis were registered from two more buccinid species: Buccinum scalariforme and Neptunea despecta. We also found metacercariae of F. agnotum and F. fellis producing eggs in the second intermediate host. Two fellodistomids were found in protobranch bivalves: sporocysts and cercariae of Steringophorus furciger in Nuculana pernula, and sporocysts with large furcocercous cercariae in Ennucula tenuis. The latter were identified as F. agnotum by molecular analysis; thus, the entire life cycle of this species was reconstructed.


Parasitology ◽  
1973 ◽  
Vol 67 (3) ◽  
pp. 341-350 ◽  
Author(s):  
R. A. Matthews

Bucephalus haimeanus is shown to be an estuarine species. The cercaria from Cardium edule is briefly redescribed to include details of the nephridial system. The metacercaria is described for the first time, having been obtained experimentally in Pomatoschistus microps and Pleuronectes platessa. In Pomatoschistus microps it survives at least 10 months, development within this host being completed within 2 months. The main site of infection is the liver. Migration is completed within 1 h and in some instances within 10 min. During this period the metacercaria actively feeds on host tissue, the gut being greatly distended with food on encystment. A hyaline cyst wall is maintained throughout the remaining life of the metacercaria. ‘O’ group plaice are highly susceptible to invasion by B. haimeanus during early summer and 100% infections were recorded in catches from Ynys-las, Dovey Estuary, in June. Experiments showed that only 2% of the metacercariae survived more than two weeks and that ‘l’ group plaice were non-susceptible to infection. Plaice are therefore considered accidental hosts. The metacercaria was linked with the adult stage from Morone labrax on the basis of comparative morphology and the ecology of the hosts, the bass entering the estuarine habitat during the summer months. The adult is considered synonymous with Bucephalus minimus Stossich, 1887.


Parasitology ◽  
1982 ◽  
Vol 84 (1) ◽  
pp. 131-135 ◽  
Author(s):  
R. Vanoverschelde

SUMMARYThe influence of temperature and salinity on miracidial longevity and miracidial infectivity of the digenean,Himasthla militaris, has been examined. At 14, 25 and 30 °C the half-life of the miracidia was 1200, 630 and 420 min respectively, and infection of the first intermediate host,Hydrobia ventrosa, only occurred at 25 and 30 °C, for both temperatures 52% became infected. In the range 2·1 to 34‰ (2·1, 4·2, 8·5, 17 and 34‰) the miracidia had a minimal and maximal half-life of 60 and 630 min in water with a salinity of 2·1 and 17‰ respectively, while the infection of the snail host was possible only in water with a salinity of 8·5 and 17‰.


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