The bionomics and parasitic development of Tripius sciarae (Bovien) (Sphaerulariidae: Aphelenchoidea), a nematode parasite of sciarid flies (Sciaridae: Diptera)

Parasitology ◽  
1965 ◽  
Vol 55 (3) ◽  
pp. 559-569 ◽  
Author(s):  
George O. Poinar

After penetrating through the body wall into the haemocoel of Bradysia paupera, the fertilized female of Tipius sciarae increased in size and slowly expelled the enlarging uterine cells through the vulva.Within 7 days of penetration, the females were mature and began laying eggs into the haemocoel of the host. The eggs hatched in 3 days and, within 2 weeks, the host–s body was swarming with juvenile nematodes. The juveniles moulted three times in the body cavity of the host and 4th-stage forms emerged through ruptures in the intestine or body wall (in larval hosts) or were deposited on the surface of the soil (by adult female flies). They then moulted to adult forms while remaining ensheathed in their last juvenile cuticle, mated, and the fertilized infective females were ready to enter a new host.Most parasitized fly larvae died before reaching the pupal stage but some emerged as adults, still carrying the nematodes within them. All parasitized adult flies were sterile. Infested larvae had smaller fat bodies and adult histoblasts than normal larvae and took twice as long to develop.Preliminary tests suggested that this nematode may be useful in controlling sciarid gnats in glasshouses.T. sciarae (Bovien) and T. gibbosus (Leuckart) were compared.This work was done at Rothamsted Experimental Station, Harpenden, Herts, England, while the author held a postdoctoral grant from the National Institutes of Health, Bethesda, Maryland. I thank Mr F. G. W. Jones for a place in the Nematology Department, Dr Audrey Shepherd for supplying the New Blue R stain, Dr J. B. Goodey for advice, and Dr K. Lindhardt, Denmark, for the loaning of the late Dr Bovien–s slides of T. sciarae.

1986 ◽  
Vol 125 (1) ◽  
pp. 137-155 ◽  
Author(s):  
Timothy Z. Vitalis ◽  
William K. Milsom

Measurements of pulmonary mechanics on anaesthetized specimens of the aquatic turtle Pseudemys scripta (Schoepff) indicate that the static pulmonary mechanics of the total respiratory system are determined primarily by the mechanics of the body wall rather than those of the lungs. This is also true under the dynamic conditions of pump ventilation at low pump frequencies. As pump frequency increases, the work required to inflate the multicameral lungs of the turtle begins to contribute an increasing portion to the total mechanical work required to produce each breath as measured from pressure volume loops. The rise in the work performed on the lungs results from an increase in the non-elastic, flow-resistive forces which must be overcome during ventilation. The primary bronchus to each lung is the most likely site of flow resistance. There is also a small elastic component to the work required to ventilate the lungs associated with movement of the intrapulmonary septa and the striated muscle surrounding the lungs. The contribution of the work required to distend the body cavity as a percentage of the total mechanical work required to generate each breath remains relatively unchanged with increasing ventilation frequency, indicating that the majority of the forces to be overcome in the body wall are elastic in nature. For a constant rate of minute pump ventilation, as frequency increases, the work done per minute to overcome elastic forces decreases, while that done to overcome non-elastic forces begins to rise. These opposing trends produce an optimum combination of pump volume and frequency at which the rate of mechanical work is minimum.


Parasitology ◽  
1970 ◽  
Vol 61 (1) ◽  
pp. 111-126 ◽  
Author(s):  
P. J. Whitfield

An adult female Polymorphus minutus releases only mature eggs into the intestine of its final host. These eggs come from the pool of eggs in the body cavity of the worm which contains only about 30% of mature eggs, the rest being immature. An analysis of the age structures of the egg populations in the body cavity and the uterus shows that an assortment of mature and immature eggs has taken place as the eggs pass from the body cavity to the uterus. The uterus contains only mature eggs and these are the eggs which are about to be released. The only pathway whereby eggs can enter the uterus from the body cavity is through the uterine bell. This suggests that it is the uterine bell which is able to select mature eggs from the mixture of eggs in the body cavity.A uterine bell in vitro engages in precisely patterned muscular activity which propels eggs through its branching lumen. In one part of the bell (the grooves between the median wall cells and the lappets of the uterine duct cells), the patterned muscular activity passes mature eggs into the uterus and immature eggs back into the body cavity to complete their development. The greater length of mature eggs seems to be the character which enables them to be ‘recognized‘ by the uterine bell.


Author(s):  
Andreas Schmidt-Rhaesa ◽  
Gerhard Pohle ◽  
Julien Gaudette ◽  
Victoria Burdett-Coutts

Nectonema species are parasites of decapod crustaceans and the only known representatives of the otherwise freshwater/terrestrial taxon Nematomorpha. We report the American lobster, Homarus americanus, as a new host for Nectonema agile, a first record among astacidean decapods. A female, about 590 mm long, was found in the body cavity of one female lobster specimen. We assume lobster to be a very rare host for Nectonema.


1881 ◽  
Vol 32 (212-215) ◽  
pp. 1-11 ◽  

In Holothuria the polian vesicle opens freely into a wide circular canal a short distance from the termination of the stone canal. From this circular canal five lozenge-shaped sinuses project forwards, and from each of these two large oval sinuses run forward parallel with each other─the ten oval sinuses becoming continuous with the hollow stems of the tentacles. Injection of the polian vesicle shows that it forms one continuous tube system with the circular canal and its sinuses, oval sinuses and tentacles, ampullæ and pedicels. Unless the pressure is kept up for a considerable time there is no penetration of the injected fluid into the stone canal, and either the ring, the vesicle, or a sinus gives way before the fluid reaches the madreporic plate. Specimens injected with a gelatine mass show that each canal sinus opens into a cæcal tube, which runs forwards internal to the sinuses of the tentacles as far as a wide circum-oral space. This space communicates by well-defined apertures with that portion of the body cavity which lies between the sinuses and the œsophagus, and which is reached through the circular apertures between the sinuses of the circular canal. Each canal sinus has three other apertures in its walls. It opens by a small round aperture into a radial canal, and the two other apertures occur as minute slits, one at each side of the orifice of the radial canal leading into the adjacent tentacle sinuses. When the tentacle into which the sinus opens is protruded, there is no constriction between the sinus and the tentacle ; but when the ten­tacle is retracted, there is a well-marked constriction at the junction of the sinus with the tentacle. The eversion of the perisome and the protrusion of the tentacles are effected chiefly by the shortening of the polian vesicle and the constriction of the longitudinal muscular bands, which run from the inner surface of the body wall between each two adjacent tentacle-sinuses ; but the circular fibres of the body wall also assist in the process by contracting immediately behind the group of sinuses, so as to act on them by direct pressure, and also indirectly by forcing the body fluid against them.


Parasitology ◽  
1933 ◽  
Vol 25 (3) ◽  
pp. 342-352 ◽  
Author(s):  
Mary E. Fuller

The life history of Onesia accepta Mall. is described. This species is parasitic on the earthworm Microscolex dubius Fletcher. The first and second larval instars are passed under the skin and the third instar in the body cavity of the host. The feeding period of the maggot is approximately 20 days, and the pupal stage about 12 days.The external morphology of the three larval instars and of the puparium is described in detail.


Plastron-bearing spiracular gills have been independently evolved in two groups of the Psephenidae, the Psephenoidinae and one genus of the Eubriinae. The spiracular gills of the pupae are exclusively spiracular structures. The plastron is on the spiracle rather than on the body wall adjacent to the spiracle, as in the pupae of flies. In some species the spiracular gills are borne at the end of projections from the body wall. In one genus of Eubriinae, epidermal cells that remain in good condition are isolated in the projections from the body wall in such a way that they are completely separated by a thick wall of cuticle from the remaining tissues of the body in both the pupal stage and in the pharate adult stage. The origin of plastron respiration in the Psephenidae is discussed. Non-aquatic pupae are found near the edges of streams where they are apt to be flooded by rises in stream level. The water/air interface of normal spiracles is too small (400 to 1100 μm 2 /mg) to satisfy oxygen demands by extracting oxygen from the ambient water when they are flooded. The water/air interface of the least well-developed plastrons in insects is equivalent to about 15000 μm 2 /mg of body weight. It is suggested that every increase in the length of the spiracles has a selective advantage in that it enables the pupa to utilize atmospheric oxygen when covered by correspondingly thicker layers of water. At some stage in this process, plastron respiration through the spiracles becomes significant in satisfying oxygen demands. When this stage is reached, selective pressures begin to operate directly to increase the water/air interface of the spiracles. It is shown that if all spiracles of some forms, such as Metaeopsephenus , were like its longest spiracles, the linear dimensions of the spiracles would only have to be increased by a factor of 2*2 for these to have a water/air interface per mg of body weight equivalent to that of some insects with plastrons. Spiracles that do not function in gas exchanges between the insect and the ambient environment nevertheless persist because they subserve two other functions: ( a ) when they are first formed their chambers or ecdysial tubes provide a lumen through which the old tracheae of the previous instar may be withdrawn, and ( b ) after the appearance of the new instar their chambers, now collapsed, are the means by which the tracheae of the previous instar are anchored to the cuticle that is to be shed. Spiracles that do not function in gas exchanges and have their orifices closed are known as non-functional spiracles. Once a spiracle becomes non-functional in a particular instar it remains non-functional in that instar despite the fact that it is temporarily open between the moult and the ecdysis. The loss of functional spiracles is irreversible irrespective of changes in the habits or environment of the group. Examples of irreversible losses of functional spiracles are cited that concern more than one million cases. In some Psephenidae the spiracles of the first abdominal segment are non-functional. The spiracular atrium and the regulatory apparatus of such spiracles may nevertheless persist and be more or less identical in structure to those of functional spiracles. The evidence suggests that in the subfamily Eubriinae such non-functional structures have persisted since at least the Eocene. Plastron-bearing spiracular gills are polyphyletic in origin. They have been independently evolved at least nine times in the Diptera and twice in the Goleoptera. In the Diptera spiracular gills are modifications of the body wall adjacent to the spiracle (e.g. Tanyderidae, Deuterophlebiidae, and Simuliidae) or of both the body wall and the spiracle (e.g. Tipulidae). In the Coleoptera they are modifications of the spiracle only although the spiracle may be borne on a long projection from the body wall (e.g. Psephenoides volatilis Champ). Because in each group of insects the spiracular gills are independently evolved, a phylogenetic classification of these gills is excluded, but a classification of convenience is proposed.


1924 ◽  
Vol s2-68 (269) ◽  
pp. 147-186
Author(s):  
H. R. MEHRA

1. The genital organs of Stylaria lacustris are described in detail. The vas deferens opens into the atrium on the anterior face near the opening of the ejaculatory duct and not at the top as described by all the previous authors. The prostate surrounds not only the atrium but also the vas deferens in segment 6. 2. The prostate secretion passes through the atrial epithelium, which consequently hypertrophies and disappears 3. The development of the genital organs proceeds with great rapidity when the sexual phase appears, which occurs only once a, year from the end of September to the beginning of December. There is no long intervening period between the development of the gonads, and other genital organs. 4. The order of development seems to be connected with the time or order of their functioning. 5. The gonads are peritoneal in origin. The sperm-sac and orisac are large portions of the body-cavity enclosed by the extension backwards of septa ⅚ and 6/7 respectively. The yolk-mass is formed by a process of metabolic change in the cytoplasm of some of the ova. 6. The sperm-duct is partly peritoneal in origin and partly an ectodermal invagination. The funnel and the vas deferens rudiments arise by a proliferation of the peritoneal cells on the anterior face of septum ⅚, which assumes the form of a deeply shining plate of columnar cells with prominent nuclei. This after the funnel rudiment becomes the sperm-cord and penetrates the septum in front of the ovary, reaching near the body-wall the atrial rudiment, which is soon formed as an ec todermal invagination. The prostate cells arise from the peritoneum near the rentral body-wal1 of the sixth segment in the neighbourhood of the atrial rudiment. 7. The rudimentary female funnel, which opens ont at the female opening, arises as, an outgrowth from the peritoneum at the base of septum 6/7. 8. The spermatheca srises as an invagination from the ectoderm. I agree with Bergh that the sperm, zthecae are to be considered as new structures, and not phylogenetically connected with the genital ducts as Gatenby supposes to be the case in Tubifex rivulorum. 9. A fern stages obtained showing the development of these organs in Nais e1inguis confirm the above observntions.


Parasitology ◽  
1966 ◽  
Vol 56 (4) ◽  
pp. 657-664 ◽  
Author(s):  
Trond Bråten

Investigations on the host specificity of plerocercoids of Schistocephalus solidus were carried out using the technique of surgically transferring plerocercoids from the body cavity of Gasterosteus aculeatus to various other fish. Plerocercoids survived in all cases when transferred from G. aculeatus to other G. aculeatus; when tranferred to Pungitius pungitius the worms survived for long periods but failed to grow. Plerocercoids transferred to Coitus gobio, Nemacheilus barbatula, Phoxinus phoxinus, Salmo trutta, Coregonus clupeoides, Perca fluviatilis, Rutilus rutilus and Esox lucius always died within 2–10 days after being transferred. Electron-microscopic examinations of the tegument of plerocercoids transferred to new hosts showed: in G. aculeatus normal appearance throughout the experiment; in P. pungitius degeneration of the microtrichs after 6 days; and in S. trutta complete destruction of the tegument in 7 days.Plerocercoids of the genus Diphyllobothrium survived the transfer from Gasterosteus aculeatus to Salmo trutta and continued to grow in their new host.Infection of fish with S. solidus by feeding infected copepods and by aspetic injection of procercoids into the body cavity of the fish were also tried. Gasterosteus aculeatus became infected using both these methods but it was not possible to infect Pungitius pungitius.


Parasitology ◽  
1974 ◽  
Vol 69 (3) ◽  
pp. 417-427 ◽  
Author(s):  
J. W. Lewis ◽  
D. R. Jones ◽  
J. R. Adams

Using biomedical techniques experimental determinations of the hydrostatic pressure in the pseudocoel of adult female Philonema oncorhynchi indicated that the rate of increase in pressure (dP/dT) and absolute pressure values (cm/H2O) shown by bursting worms in distilled water are correlated with the diameter of the nematode. At bursting pressures, wall tension in a wide size range of worms was virtually identical, indicating that the bursting process is independent of muscular contraction. That the generation of the hydrostatic pressure was an osmotic phenomenon was confirmed by measuring dP/dT in prelarvigerous and larvigerous female worms subjected to different concentrations of sodium chloride, ranging from 89 to 800 m-osmol/kg, and also to a variety of solutions of similar osmolarity (155–175 m-osmol/kg), e.g. magnesium sulphate, urea, potassium chloride, sodium chloride and sucrose. The overall rate of uptake was faster in the larger worms but, per unit surface area, small worms had an uptake rate three times that of the large individuals.The prediction that the body wall of female P. oncorhynchi is permeable to ions such as Na+ was confirmed using radiolabelled 22Na and by bringing about changes in the osmolarity of worms subjected, for 5 min periods, to hyperosmotic solutions of sodium chloride and sucrose. The survival of P. oncorhynchi in the body cavity of sockeye salmon, Oncorhynchus nerka, is dependent upon the permeable nature of the body wall of P. oncorhynchi allowing the worm to function as an ‘osmometer', because as the anadromous O. nerka enters fresh water, the osmolarity of its blood plasma is known to decrease by about 15%. At the time of spawning in Cultus Lake, British Columbia, the body fluids of both female P. oncorhynchi and O. nerka are isosmotic, indicating that the worms are able to equilibrate to the above changes and at the same time preventing premature bursting in the body cavity of its host. However, osmotic invasion of water must occur far quicker than ionic exchange since complete release of larvae does take place when female worms pass out into the redd along with the eggs of the fish and burst.


1985 ◽  
Vol 33 (2) ◽  
pp. 153 ◽  
Author(s):  
WG Inglis

Concordant patterns of embryology, morphology and functional anatomy delimit grades of animal phyla, each of which contains a 'Major Phylum': PARACOELOMATA (nom.nov.) = acoelomates + pseudocoelomates, flexible hydrostatic skeleton, Nematoda; DEUTEROSTOMIA (including lophophorates) = enterocoelic coelom, rigid internal skeleton, Chordata; and PROTOSTOMIA with two subgrades, MONOMERIC P. = unsegmented, single coelom, molluscan blastular cross, partial rigid exoskeleton, Molluscs; and POLYMERIC P. = segmented, multiple coelom, annelid cross, rigid exoskeleton, Uniramia. Such groups are usually treated as arbitrary stages in mono- and limited-branch phylogenies, but recent studies show them to be real and significant because the only phylogenetic links are from each Paracoelomata and Protostomia Phylum to Turbellaria; and each Deuterostomia Phylum to Cnidaria-Ctenophora and/or enteropneust Hemichordata. Similar grades have often been explained by hypothetical common ancestors, which are unnecessary if the phyla arose during 'evolutionary waves'. These attribute the origin of each grade to the likelihood that its constituent phyla arose independently, about the same time, from the same ciliary powered ancestral stock which was preadapted to enabling a potential body cavity to be actualized while evolving a cylindrical, wholly muscle-powered, body with a hydrostatic skeleton. Because such a skeleton is functionally dependent upon other structural modifications, particularly of the body wall, it could appear only when these were also available. If the latter could be supplied in a number of ways, all opportunities would be exploited and a body cavity would appear several times. The morphology suggests that this did happen, so that a pseudocoelom and coelom evolved independently in each phylum where they occur. Because of evidence that Protostomia and Deuterostomia were never linked during evolution, the origin of the coeloms in the former are explained by the Gonocoelic Theory and in the latter by the Enterocoelic. This, with the recognition of the monomeric protostomes as a distinct group, establishes that segmentation arose at the same time as the coeloms, so that their origins are one problem and not two as usually thought. Finally, protistan data suggest that Turbellaria, and so Paracoelomata and Protostomia, arose from 'close mitosis' flagellates, as did Fungi; while Cnidaria, and so Deuterostomia, arose from 'open mitosis' flagellates. as did Plantae. Thus, the classic Animalia division into Protostomia and Deuterostomia may represent a Protista division such that the animal groups are closer to fungi and plants respectively than they are to each other.


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