The prepupal Stage in Ichneumonidae, illustrated by the life-history of Exenterus abruptorius, Thb.

1937 ◽  
Vol 28 (4) ◽  
pp. 525-534 ◽  
Author(s):  
K. R. S. Morris

A full description is given of the life-history of Exenterus abruptorius, Thb., an important parasite of the pine sawfly, Diprion sertifer, Geoff.The insect is univoltine, like the host. It oviposits on the last stage larva or prepupa and only hatches after the host has spun its cocoon. Only one-quarter of the primary larvae develop immediately, the remainder resting up to two and a-half months during the summer before proceeding with their development. On the completion of feeding the parasite larva spins its cocoon within the host cocoon and enters the prepupal stage, which can be divided into two distinct phases, eonymphal and pronymphal. Hibernation is always in the eonymphal stage. In Sweden 37 per cent. of this species remained in hibernation for two winters, but in Hungary all emerged in the spring following the year of development. Further than this, in Sweden the sexes were in approximately equal proportions; in Hungary females exceeded males by four to one. This may indicate the existence of biological races.Other Ichneumonidae exhibit the prepupal stage, with eonymphal and pronymphal phases, in their development. The typical facies of this is analogous to that in the prepupal stage in Tenthredinidae, in which, however, ecdysis precedes this stage, which is then a distinct instar. It is suggested that an instar is lost in the development of the Ichneumonidae, though the facies of the prepupal stage is retained.

1917 ◽  
Vol 8 (2) ◽  
pp. 121-123 ◽  
Author(s):  
D. Keilin

It has been well known since the studies of Taschenberg (1864–1872) that the larvae of Leptohylemyia coarctata, Fall., attack wheat and rye. The damage due to this fly has been observed many times in almost all European countries, and many papers have been devoted to its life-history. Of these papers the most important are those of E. Ormerod (1882–1895), S. Rostrup (1905–1911), T. Hedlund (1906- 1907), P. Marchal (1909) and finally the recent work of Kurdjumov (1914).


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.


Parasitology ◽  
1953 ◽  
Vol 43 (1-2) ◽  
pp. 148-159 ◽  
Author(s):  
B. Jobling

At one of the meetings of the Royal Society of Tropical Medicine and Hygiene, I made a very short communication on the three blood-sucking midges (Jobling, 1929). My particular reference was to Culicoides vexans, which is the most troublesome and commonestspecies in spring, in the northern and the north-western suburbs of London. At that time I had been studying the life history of this midge, including the morphology of its eggs, larvae and the pupa, but this work was not completed.


1934 ◽  
Vol s2-77 (306) ◽  
pp. 273-304
Author(s):  
W. H. THORPE

1. In a previous paper was described the life-history of Cryptochaetum iceryae parasitic on Icerya purchasi, an Australian species introduced into California. It was shown that the genus is highly specialized for life as a parasite, and that it represents a separate and restricted line of evolution of parasitic habits among insects. The present study concerns Cryptochaetum grandicorne which is probably confined to the Mediterranean region, and which is the only species of the genus known to occur in Europe. The two species show notable differences in structure and life-history although both are highly adapted to a parasitic mode of life. 2. The very minute eggs are laid in the haemocoel of the host. The egg hatches to form a short-lived ‘embryo-larva’ at first atracheate and showing no trace of external segmentation. Mouth parts are present although the fore-gut is closed, food materials presumably being absorbed by diffusion from the blood of the host. 3. The second stage larva is tracheate but apneustic. Segmentation is complete. The fore-gut is now open but the hindgut remains closed. The food consists of the blood and fat-body of the host. 4. The third stage larva is omnivorous devouring the internal organs of the host indiscriminately and the hind-gut is open. The tracheal system is amphipneustic. A few days after the commencement of the instar the posterior spiracles pierce the skin of the host and establish connexion with the atmospheric air. The puparium is formed within the dead body of the host. 5. As in Cryptochaetum iceryae the larva is supplied with a pair of long tubular caudal filaments, lobes of the bodywall containing blood and tracheae, which arise from the posterior segment and ramify among the organs of the host. Experiments indicate that they serve to increase the surface area available for respiratory exchange between the larva and the blood of the host. They are also readily permeable to water. 6. Although a large number of eggs may be placed within a single host, only one reaches maturity. 7. The highly specialized ovipositor is described in detail since it appears to be a striking adaptation to a parasitic mode of life, and cannot be derived directly from the rasping ovipositor of the Agromyzidae. 8. In South Italy as in South France there is one generation per year, the life-history of the parasite being closely correlated with that of the host. 9. Special attention is paid to those features in which grandicorne differs from iceryae and the significance of these differences is discussed.


2019 ◽  
Vol 96 (2) ◽  
pp. 533-538
Author(s):  
Pietro Battaglia ◽  
David Smith ◽  
Giovanni Ammendolia ◽  
Mauro Cavallaro ◽  
Teresa Maggio ◽  
...  

1961 ◽  
Vol 39 (5) ◽  
pp. 579-587 ◽  
Author(s):  
S. P. Gupta

Using the ferret as an experimental host, the life cycle of Molineus barbatus was shown to be direct. All stages are described. The third-stage larva infects the host orally or percutaneously and subsequent stages develop in the mucosa of the small intestine. The male matures earlier than the female and eggs are laid in 8 to 13 days after infection. The parasite is highly pathogenic to ferrets but apparently less so to skunks and racoons.


1926 ◽  
Vol 4 (4-5) ◽  
pp. 191-198 ◽  
Author(s):  
T. Goodey

In an earlier paper (Goodey, 1924), the writer has given an account of the morphology of the adults of Œsophagostomum dentatum, the development and structure of the free-living larvæ and the biology of the ensheathed infective stage. So far, however, the parasitic larval stages have not been described. In the present paper some of the gaps in our knowledge of the complete life-history of the worm represented by these stages are filled in, not as completely as could be desired owing to the absence from the material of specimens showing the 3rd and 4th ecdyses. The worms found, however, show that the 4th stage larva has a provisional buccal capsule essentially similar to that found in 4th stage larvæ of O. radiatum (Marotel, 1908) and O. columbianum (Veglia, 1924), and in this respect is in line with certain other 4th stage larvæ of the Strongyloidea such as Ancylosloma duodenale (Looss, 1897), and Triodontophorus tenuicollis (Ortlepp, 1925), in which provisional buccal capsules built on the same general plan have been observed.


1947 ◽  
Vol 38 (1) ◽  
pp. 145-155 ◽  
Author(s):  
F. J. Simmonds

In a previous paper (Simmonds 1946*) the biology of Phytodietus pulcherrimus (Cress.), a parasite of Loxostege sticticalis, L., the sugar-beet web-worm, has been described. This paper will be devoted to the habits and life-history of another important parasite of Loxostege in North America, Bracon vulgaris (Cress.). This species appears to be confined to the American continent, all of the records being from Canada and the U.S.A. It has been reared only from Loxostege sticticalis, L., and L. commixtalis, Wlk. From the former species it has been recorded by Paddock (1912), Swenk (1918), Jones, Hoerner and Corkins (1921), Pepper and Hastings (1941), and Simmonds (1946); from the latter species by Hoerner (1933). During the present work it has been reared from L. sticticalis, material from both Montana and Alberta.


1969 ◽  
Vol 58 (3) ◽  
pp. 421-430 ◽  
Author(s):  
Dilip Kumar Dutt

An account is given of the life-history of Agrilus acutus (Thnb.) (Buprestidae), a pest of ‘mesta’ (Hibiscus cannabinus) in india. The eggs are ovate and scale like, and are laid singly on the stem, usually near a leaf scar, and when kept at 31°C. and 73 per cent. relative humidity hatched on average in 12.4 days. The larva bores through the lower surface of the egg directly into the stem and feeds under the bark forming a sprial tunnel. A raised weal develops on the surface of the stem overlying the tunnel. Before each moult, the larva bores into the wood and makes a vertical chamber in which moulting occurs. There are normally three moults in the active feeding stages, but exceptionally four, and a prepupal moult. The rate of tunnelling is at first about 56 mm. per day and later eaches about 107 mm. The larval stage lests 26 days. The fully grown larva is 21 mm. long and bores into the wood to pupate, making a pupal chamber 11 mm. long into which it fits itself by adopting an asymmetrical U-shaped posture. After a prepupal stage of 2.5 days it pupates. The pupal period occupies about 11.7 days and a further seven days are spent by the adult in the pupal chamber. The adult female mates within a day of emergence from the stem. but does not oviposit until at least seven days have elapsed.


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