ON THE MORPHOLOGY AND LIFE HISTORY OF PHOCANEMA DECIPIENS (KRABBE, 1878) MYERS, 1959 (NEMATODA:ANISAKIDAE)

1960 ◽  
Vol 38 (2) ◽  
pp. 331-344 ◽  
Author(s):  
B. J. Myers

Phocanema (synonyms: Porrocaecum, Terranova) decipiens is described in detail and its probable life cycle outlined. Eggs deposited in salt water develop and hatch in 7 to 14 days at between 10 °C and 24 °C, even after previous freezing. Temperatures over 24 °C are lethal. Larvae fed to a large variety of invertebrates passed quickly through their intestines still alive; fed to fish, they disappeared within 24 hours but in one case a larva was found ensheathed in the intestine. No larvae were found in 'wild' invertebrates although many were infected with free-living nematodes. It is concluded that, while numerous invertebrates may act as 'transport' hosts for the larva to a fish, none acts as a true intermediate host. While larvae infective to seals occur commonly in the muscles of cod, a large variety of other fish are also infected and are a more probable source of infection. Development to maturity in the seal takes approximately three weeks, and it is probable that the main source of the infection in the Gulf of St, Lawrence is the harp seal, although harbor and grey seals also contribute to it.

2005 ◽  
Vol 79 (2) ◽  
pp. 169-176 ◽  
Author(s):  
J.A. Shears ◽  
C.R. Kennedy

AbstractPrevious studies on the life history of the nematode eel specialist Paraquimperia tenerrima (Nematoda: Quimperiidae) have failed to determine whether an intermediate host is required in the life cycle. In the laboratory, eggs failed to hatch below 10°C, hatching occurring only at temperatures between 11 and 30°C. Survival of the free-living second stage larvae (L2) was also temperature dependent, with maximal survival between 10 and 20°C. Total survival of the free-living stages (eggs and L2) is unlikely to exceed a month at normal summer water temperatures, confirming that parasite could not survive the 6 month gap between shedding of eggs in spring and infection of eels in early winter outside of a host. Eels could not be infected directly with L2, nor could a range of common freshwater invertebrate species. Third stage larvae (L3) resembling P. tenerrima were found frequently and abundantly in the swimbladder of minnows Phoxinus phoxinus from several localities throughout the year and were able to survive in this host in the laboratory for at least 6 months. Third stage larvae identical to these larvae were recovered from minnows experimentally fed L2 of P. tenerrima, and eels infected experimentally with naturally and experimentally infected minnows were found to harbour fourth stage larvae (L4) and juvenile P. tenerrima in their intestines. Finally, the whole life cycle from eggs to adult was completed in the laboratory, confirming that minnows are an obligate intermediate host for P. tenerrima.


1972 ◽  
Vol 46 (1) ◽  
pp. 35-46 ◽  
Author(s):  
S. C. Dutt ◽  
H. D. Srivastava

The life cycle of Gastrodiscoidcs hominis has been described using Helicorbis coenosus as the experimental intermediate host and the pig as the definitive host.The morphology of the miracidium, redia and metacercaria has been described. Data have been furnished on the infection and longevity, of and production of cercariae by the snail host, and the growth and development of the adult-fluke in the definitive host.


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.


1978 ◽  
Vol 52 (3) ◽  
pp. 251-259 ◽  
Author(s):  
R. Madhavi

ABSTRACTThe life cycle of Genarchopsis goppo a hemiurid trematode found in the stomach of Channa punctata has been worked out in detail. The egg contains a fully developed miracidium at the time of liberation. The miracidium contains a ciliated covering, a long apical gland and a crown of spines at the anterior end. The snail Amnicola travancorica acts as the first intermediate host inside which the miracidium passes through sporocyst and redial generations. The cercaria is of cystophorous type and is identical to Cercariae Indicae Sewell XXXV. Metacercaria occurs in the ostracods Stenocypris malcolmsoni and Eucyoris capensis. The fish Aplocheilus panchax serves as the paratenic host. The entire developmental cycle from egg to egg producing adult takes 3 months.


Parasitology ◽  
1932 ◽  
Vol 24 (2) ◽  
pp. 210-224 ◽  
Author(s):  
Cecil A. Hoare

This paper contains a report on a collection of parasitic protozoa from the blood of some vertebrate animals of Uganda.Seven new species and a number of parasites recorded for new hosts are described. New observations on some known parasites are also recorded.An account is given of the life history of the crocodile haemogregarine. It is shown that the schizogony of Hepatozoon pettiti (nomen novum for Haemogregarina pettiti) occurs in the liver of the crocodile, while the sporogony takes place in Glossina palpalis, its intermediate host.A list of all the blood parasites found, together with their hosts, is given.


Author(s):  
J. B. Brown-Gilpin

The wide variety of reproductive patterns and behaviour in the many species of Nereidae already studied clearly justifies further research. But the life history of Nereis fucata (Savigny) is not only of interest from the comparative point of view. Its commensal habit (it occurs within shells occupied by hermit crabs) immediately gives it a special importance. This alone warrants a detailed study, particularly as no commensal polychaete has yet been reared through to metamorphosis and settlement on its host (Davenport, 1955; Davenport & Hickok, 1957). The numerous interesting problems which arise, and the experimental methods needed to study them, are, however, beyond the range of a paper on nereid development. It is therefore proposed to confine the present account to the reproduction and development up to the time when the larvae settle on the bottom. The complete life cycle, the mechanism of host-adoption, and related topics, will be reported in later papers.


1953 ◽  
Vol 31 (4) ◽  
pp. 351-373 ◽  
Author(s):  
Liang-Yu Wu

A cause of swimmer's itch in the lower Ottawa River is Trichobilharzia cameroni sp. nov. Its life cycle has been completed experimentally in laboratory-bred snails and in canaries and ducks, and the various stages are described. The eggs are spindle-shaped. The sporocysts are colorless and tubular. Mother sporocysts become mature in about a week. The younger daughter sporocyst is provided with spines on the anterior end and becomes mature in about three weeks. The development in the snail requires from 28 to 35 days. A few cercariae were found to live for up to 14 days at 50 °C., although their life at 16° to 18 °C. was about four days. Cercariae kept at room temperature for 60 to 72 hr. were found infective. The adults become mature in canaries and pass eggs in about 12 to 14 days. Physa gyrina is the species of snail naturally infected. It was found in one case giving off cercariae for five months after being kept in the laboratory. Domestic ducks were found to become infected until they were at least four months old, with the parasites developing to maturity in due course; no experiments were made with older ducks. Furthermore, miracidia were still recovered from the faeces four months after the duck had been experimentally infected, and it is suggested that migratory birds are the source of the local infection.


1938 ◽  
Vol s2-80 (319) ◽  
pp. 459-478
Author(s):  
CATHERINE HAYES

1. A large free-living amoeba found by Mr. Harry Watkinson in the tropical fish tanks of Mr. Albert Sutcliffe of Grimsby has been identified as Amoeba discoides (Schaeffer, 1916) = Metachaos discoides (Schaeffer, 1926). 2. From the inoculation material obtained from these tanks Amoeba discoides has been successfully cultivated in the Notre Dame Training College Laboratory by a technique similar to that used for the cultivation of Amoeba proteus: wheat being the pabulum employed. In contrast to what obtains in the cultivation of Amoeba proteus , however, Amoeba discoides flourishes more luxuriantly in shallow Petri dishes, than in deeper troughs. 3. The nucleus in the resting and dividing stages is described; division is amitotic. 4. The more important cytoplasmic contents, including nutritive spheres, and crystals are likewise described. 5. The life-history has been worked out. The adult amoeba becomes an agamont giving rise to agametes which eventually grow into adult amoebae, the life-cycle occupying roughly about four months. 6. Descriptions of the nucleus of the newly hatched and developing amoebae are deferred. I wish to offer my sincerest thanks to Professor Graham Kerr under whom this work was begun, and who has continued from afar to watch over it with ever kindly interest and encouragement and who has read the paper in typescript. My thanks are also extended to Professor Hindle, under whom the work was completed, for his kind advice and for reading the paper in typescript. In conclusion I would like to express my appreciation of her skill and of the care and trouble bestowed by Miss Brown Kelly in the execution of the original drawing of fig. 1, PI. 31.


Parasitology ◽  
1953 ◽  
Vol 42 (3-4) ◽  
pp. 244-258 ◽  
Author(s):  
J. F. A. Sprent

The development of Ascaris devosi, a parasite of the fisher and marten, was followed from the egg to the adult stage using the white mouse and the ferret as the intermediate and final hosts respectively. The eggs contained motile 1st stage larvae 6 days after cleavage and were infective at 12 days, the 1st moult having already occurred. The eggs remained infective for at least 1 year. The 2nd stage larva after hatching from the egg in the intestine of the mouse passes through the intestinal wall to the liver and mesenteric tissues. At 3 days after infection they were recovered from the heart, lungs, brain, kidneys and from the carcass. The larvae grow and store food material during the 2nd stage and between 8 and 12 days after infection they undergo the 2nd moult. The mouse shows the most severe pulmonary symptoms on the 3rd and 4th days after infection, the lungs showing complete red hepatization at this time. The 3rd stage larva is relatively inactive and becomes encapsulated in various tissues, particularly in the muscular and subcutaneous tissues of the neck, shoulders and thorax. The chief developmental changes, apart from growth, which occur in the 2nd and 3rd stage larvae are: (i) the intestine develops from a single row of cells to a multi-cellular tube; (ii) the body cavity appears; (iii) the excretory lobes appear, the nucleus on the left side becoming prominent at the end of the 2nd stage; (iv) the cuticle shows transverse striations at the end of the 2nd stage; (v) the lateral lines become prominent.The encapsulated 3rd stage larvae remained alive for at least six months in the tissues of mice and at 25 days after infection of the mouse they were able to develop in the young ferret following killing and ingestion of the mouse. No infection of ferrets was obtained through oral administration of embryonated eggs or 3rd stage larvae digested from mouse tissues.The 3rd moult occurred in the intestine of the young ferret 3–4 days after infection; in adult ferrets the 3rd stage larvae were evidently unable to gain a hold and were passed out in the faeces. In the next 2–3 weeks the larva grew from about 2 to 16 mm. the 4th moult occurring between 2 and 3 weeks after infection. During the 4th stage the lips develop into the adult form and sexual differentiation occurs. In the female the genital rudiment moves forward and becomes differentiated into the vagina, uteri and ovaries. The vulva remains closed throughout the 4th stage.The adult parasites had developed to sexual maturity by 56 days after infection, but they continued to grow and were considerably longer at 6 months after infection. The position of the vulva relative to the body length was found to move from about midway along the body in the 4th stage larva to a position at the junction of the anterior and middle third of the body in the mature adult.The life history of this parasite is discussed in relation to that of A. lumbricoides and other species. It is considered that the life history of A. devosi, requiring as it does a true intermediate host for its completion, provides further information on the evolutionary development of the ascaris group. This work accordingly supports the hypothesis that the earliest members of this group utilized an intermediate host and does not support that which supposes that ascaris parasites are descended from skin-penetrating forms.During this investigation the writer has benefited considerably from correspondence with Dr J. D. Tiner, Department of Zoology, University of Illinois, Urbana, Illinois, U.S.A. His thanks are also due to Dr H. B. Speakman and Dr A. M. Fallis for their encouragement, guidance and help.This work was supported by the Province of Ontario on the recommendation of the Research Council of Ontario.Grateful acknowledgement is made to Mr Cliff Smith of the Connaught Medical Research Laboratories of the University of Toronto for photographic work.


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