Cercaria vaullegeardi Pelseneer, 1906 (Digenea: Hemiuridae); the daughter sporocyst and emergence of the cercaria

Parasitology ◽  
1980 ◽  
Vol 81 (1) ◽  
pp. 61-69 ◽  
Author(s):  
B. F. Matthews

SUMMARYThe daughter sporocyst of Cercaria vaullegeardi has hitherto been regarded as occurring within the haemocoel of the digestive gland of Gibbula umbilicalis. A re-examination has shown that an important part of the sporocyst, previously overlooked, extends from the digestive gland, through the afferent renal vein, the right kidney haemocoel and the transverse pallial vessel into the blood channel within a gill filament, thus providing a means of exit from the host directly into the mantle cavity. The sporocyst is described at light and electron microscope levels, and the emergence of the cystophorous cercariae is discussed.

Author(s):  
J.A. Eades ◽  
A. van Dun

The measurement of magnification in the electron microscope is always troublesome especially when a goniometer stage is in use, since there can be wide variations from calibrated values. One elegant method (L.M.Brown, private communication) of avoiding the difficulties of standard methods would be to fit a device which displaces the specimen a small but known distance and recording the displacement by a double exposure. Such a device would obviate the need for changing the specimen and guarantee that the magnification was measured under precisely the conditions used.Such a small displacement could be produced by any suitable transducer mounted in one of the specimen translation mechanisms. In the present case a piezoelectric crystal was used. Modern synthetic piezo electric ceramics readily give reproducible displacements in the right range for quite modest voltages (for example: Joyce and Wilson, 1969).


Author(s):  
Richard E. Hartman ◽  
Roberta S. Hartman ◽  
Peter L. Ramos

The action of water and the electron beam on organic specimens in the electron microscope results in the removal of oxidizable material (primarily hydrogen and carbon) by reactions similar to the water gas reaction .which has the form:The energy required to force the reaction to the right is supplied by the interaction of the electron beam with the specimen.The mass of water striking the specimen is given by:where u = gH2O/cm2 sec, PH2O = partial pressure of water in Torr, & T = absolute temperature of the gas phase. If it is assumed that mass is removed from the specimen by a reaction approximated by (1) and that the specimen is uniformly thinned by the reaction, then the thinning rate in A/ min iswhere x = thickness of the specimen in A, t = time in minutes, & E = efficiency (the fraction of the water striking the specimen which reacts with it).


2017 ◽  
Vol 16 (2) ◽  
pp. 174-177 ◽  
Author(s):  
Satheesha Badagabettu Nayak ◽  
Ashwini Aithal Padur ◽  
Naveen Kumar ◽  
Deepthinath Reghunathan

Abstract Variations of the testicular veins are relevant in clinical cases of varicocele and in other therapeutic and diagnostic procedures. We report herein on a unique variation of the left testicular vein observed in an adult male cadaver. The left testicular vein bifurcated to give rise to left and right branches which terminated by joining the left renal vein. There was also an oblique communication between the two branches of the left testicular vein. A slender communicating vein arose from the left branch of the left testicular vein and ascended upwards in front of the left renal vein and terminated into the left suprarenal vein. The right branch of the testicular vein received an unnamed adipose tributary from the side of the abdominal aorta. Awareness of these venous anomalies can help surgeons accurately ligate abnormal venous communications and avoid iatrogenic injuries and it is important for proper surgical management.


1979 ◽  
Vol 70 (7) ◽  
pp. 799-809
Author(s):  
Fujio Masuda ◽  
Hideo Hishinuma ◽  
Tadamasa Sakai ◽  
Yoshikazu Arai ◽  
Ryo Shoji ◽  
...  
Keyword(s):  

2018 ◽  
Vol 6 (11) ◽  
pp. 1946-1952
Author(s):  
Ali Yilmaz ◽  
Abdullah Topcu ◽  
Cagdas Erdogan ◽  
Barbaros Sahin ◽  
Gulcin Abban ◽  
...  

AIM: There are many trials concerning peripheral nerve damage causes and treatment options. Unfortunately, nerve damage is still a major problem regarding health, social and economic issues. On this study, we used vascular graft and human cord blood derived stem cells to find an alternative treatment solution to this problem. MATERIAL AND METHODS: We used 21 female Wistar rats on our study. They were anesthetized with ketamine and we studied right hind limbs. On Group 1, we did a full layer cut on the right sciatic nerve. On Group 2, we did a full layer cut on the right sciatic nerve, and we covered synthetic vascular graft on cut area. On Group 3, we did a full layer cut on right sciatic nerve, and we covered the area with stem cell applied vascular graft. RESULTS: At the end of postoperative 8. weeks, we performed EMG on the rats. When we compared healthy and degenerated areas as a result of EMG, we found significant amplitude differences between the groups on healthy areas whereas there was no significant difference on degenerated  areas between the groups. Then we re-opened the operated area again to reveal the sciatic nerve cut area, and we performed electron microscope evaluation. On the stem cell group, we observed that both the axon and the myelin sheet prevented degeneration. CONCLUSION: This study is a first on using synthetic vascular graft and cord blood derived CD34+ cells in peripheral nerve degeneration. On  the  tissues  that  were  examined  with  electron  microscope,  we  observed  that  CD34+  cells  prevented  both  axonal  and  myelin  sheath degeneration. Nerve tissue showed similar results to the control group, and the damage was minimal.


1959 ◽  
Vol 197 (5) ◽  
pp. 1093-1096
Author(s):  
Joseph H. Perlmutt

The effect of increased pressure in one kidney, produced by ligation of its vein, on contralateral renal function was investigated in eight anesthetized dogs. Kidney function was determined under the same experimental conditions in five dogs, but without renal vein ligation. For the latter group, renal function, on the average, remained reasonably stable. After left renal vein ligation, findings for the right kidney were as follows: a) decreased urine flow, amounting maximally to 9.5–41.4% of control flows; b) slight increase of questionable significance in creatinine clearance; c) inconstant changes in PAH clearance; d) increase in urine osmolality to hypertonic values; e) decrease in solute-free water clearance; f) slight rise of questionable significance in total solute clearance; and g) either no change or inconstant changes in excretion rates Na+ and K+. The data indicate that the oliguria resulted solely from increased renal tubular reabsorption of water, suggesting liberation of antidiuretic hormone as the possible mechanism. Direct nervous influences on tubular reabsorption of water cannot, however, be presently ruled out.


Three species of archaeogastropod mollusc, Monodonta lineata (da Costa), Emarginula reticulata Sowerby and Patella vulgata L. were selected as representative members of the Trochacea, Fissurellacea and Patellacea, respectively, for a comparative anatomical and ultrastructural study of the excretory system. Primary urine formation takes place by filtration of blood through the walls of the paired auricles in Monodonta and Emarginula and of the single auricle and ventricle in Patella . Urine then passes to right and left kidneys along the renopericardial canals. Contrary to earlier reports the two kidneys are different in structure and function in all three species, the larger right kidney retaining the primitive function of nitrogenous excretion, the left having a predominantly resorptive role and with a capacity to abstract from the blood solutes of larger molecular mass. The difference in the size of the two kidneys is exaggerated in Patella and Emarginula as a consequence of partial restoration of bilateral symmetry in these limpets. It has been possible to demonstrate at the ultrastructural level that the minute left kidney of Emarginula is functional. The vacuolated epithelial cells of the right kidney contain layered excretory spherules composed of purines, melanin and ferric iron in different proportions in the three genera. There is close similarity in the ultrastructural organization of these cells in Monodonta and Emarginula , but those of Patella show marked differences and their excretory spherules contain a higher proportion of melanin. The position of the left kidney in the mantle skirt, as exemplified by Monodonta , is believed to have arisen in the earliest gastropods correlated with the development of helical coiling. This was accompanied by a change in its blood vessels. It has lost its afferent renal vein, which primitively would have carried deoxygenated blood from the viscera, an arrangement which persists in the right kidney. The left efferent renal vein is reduced in Monodonta and lost in Patella and Emarginula . A new vessel has arisen linking left auricle and left kidney and there is evidence to suggest that it carries post-branchial oxygenated blood. It is believed to serve as both an afferent and major efferent route. The physiological implications of this change in the blood supply are discussed and held to be responsible for the functional differences between the two kidneys, creating conditions in the left which favour resorption of organic solutes and ions, and leaving the right kidney with the primary role of nitrogenous excretion. The evolution of the nephridial gland is examined in this context and is also believed to be correlated with the change in the blood supply to the left kidney. Ultrastructural evidence is given in support of its suggested resorptive function. The significance of the differences between right and left kidneys of archaeogastropods is discussed in relation to the evolution of the monotocardian excretory system, and the possible phylogenetic relationships of the groups of archaeogastropods are considered.


1962 ◽  
Vol 68 (3) ◽  
pp. 237-260
Author(s):  
Krishna Chandra Ghose

SynopsisOrganogenesis is completed by 15 days. A modified veliger stage is present. Torsion begins at about the sixth day. The foot rudiment is first to appear. The stomodæum appears as a new structure. The salivary glands develop from the stomodæum by evaginations. The œsophagus is stomodæal, while the crop and the primitive stomach are archenteric in origin. The digestive gland develops as two outgrowths of the primitive stomach. The hind gut is formed by the cells proliferated from the closed posterior end of the archenteron. It opens into the primitive stomach in a 2·5 mm. embryo, and the anus appears very late. The proctodæum is absent. The primordium of the pericardium with the heart, definitive kidney and gonad is mesodermal. The ureter is ectodermal and arises from the mantle cavity by evagination and subsequently communicates with the kidney. Lung and mantle are ectodermal and arise by separate invaginations. The lung fuses with the mantle and loses its separate existence from about a 4 mm. embryo. The nervous system is early to appear and the sense organs, except the statocysts are late in origin. They are ectodermal. The larval organs are: velum, podocyst, larval kidney, nuchal cells and larval digestive gland. The prototroch is the rudiment of the velum. It appears in a very early embryo from the posteroventral part and marks off the anterior border of the stomodæum. The cells of the prototroch become hyaline, vacuolate and develop cilia in a 2·25 mm. embryo, and it is transformed into velum. The velum helps in driving albumen into the larval and adult digestive glands and is resorbed in the body-wall epithelium. The rudiment of the foot first appears after the completion of gastrulation, and the podocyst is differentiated from it later. It steadily increases in size, assumes a hood-like shape, exhibits contraction and relaxation movements and begins to reduce when the embryo attains 3·25 mm. size. It is completely resorbed in the foot. The larval kidneys are mesodermal in origin, appear, in a 920 μ embryo. They begin to degenerate after the formation of the functional definitive kidney and disappear in a late larva. The kidneys are U-shaped, the cells of the closed anterior and bear pseudopodia, which are almost totally replaced by cilia afterwards. The kidney opens to the exterior posteriorly. The cells become vacuolated and excretory granules accumulate in the vacuoles. The nuchal cells first appear in a 2·5 mm. embryo and are excretory. They increase both in number and size with the growth of the embryo and persist throughout the larval period. The endoderm cells of the major portion of the archenteron except a small posterior part, enlarge in size, develop vacuoles and form a larval digestive organ for the purpose of digestion of albumen. Even after the formation of the adult digestive gland, the larval digestive gland functions for a short time, then degenerates and disappears at the end of the larval life.


2012 ◽  
Vol 94 (6) ◽  
pp. e40-e41 ◽  
Author(s):  
Ashraf El-Hinnawi ◽  
Junichiro Sageshima ◽  
Koishiro Uchida ◽  
Linda Chen ◽  
George W. Burke ◽  
...  

Excluding the isomyarian family Dimyidae, the Pectinacea comprise the families Propeamussidae, Pectinidae, Spondylidae and Plicatulidae. Present investigations are primarily concerned with species of the last two, both of which are cemented by the right valve, with secondary teeth and sockets which form ball and socket joints between the valves. Neither has previously been examined in life or the hinge and ligament critically studied. Comparing throughout with conditions in the Pectinidae, the ctenidia in Plicatula are simpler (like those of Propeamussium ) but both here and in Spondylus the ciliary pattern (type B (1a)) is more primitive. Spondylus resembles the Pectinidae in that it has elaborate arborescent lips and pallial eyes; Plicatula (and Propeamussium ) has neither, and the inner mantle folds (velum) are reduced (though enlarged in Propeamussium ). The foot is lost in Plicatula and in Spondylus has solely to do with cleansing; the Pectinidae display a range of pedal form and function - from locomotion to byssal attachment and to cleansing. The ratio of ‘quick’ to ‘catch’ muscle in the adductor is associated with habit, being greatest where need for rapid adduction is greatest, primarily in connexion with cleansing, a matter of particular urgency in horizontally disposed bivalves. Pallial eyes - as well developed in permanently attached as in swimming species - are most probably concerned with immediate response to predatory attack on pallial tissues widely exposed when the valves gape. The ligament in both Spondylus and Plicatula is surprisingly different from that in the Pectinidae (and Propeamussidae). The long anterior and posterior outer ligament layers found in the two last which unite the valves at either end of the condensed rounded inner ligament layer are replaced in Spondylus by fused periostracum . The outer ligament layers have migrated inwards and, after dividing on either side of the unchanged inner ligament layer, unite (topographically) above and below it, forming morphologically left and right areas composed equally of anterior and posterior outer ligament layers. The inward extensions of the fused periostracal grooves which form the secondary extensions to the primary ligament may well be associated with the change in nature of the hinge plate (and thus of teeth and sockets) to crossed-lamellar aragonite instead of the foliated calcite present in the Pectinidae. The combined inner and outer ligament layers produce the more powerful ligament demanded by the more massive valves; the secondary periostracal extensions serve only to unite the valves which are maintained in alinement by way of the secondary teeth and sockets. The conspicuous bilateral asymmetry in the hinge and ligament is a result of cementation; similar conditions exist in the cemented pectinid, Hinnites . In Plicatula differences are much greater. Inward growth of the mantle margins results in union above the now submarginal ligament. This is extremely compressed in the transverse plane becoming hoop-like with the right limb the longer. Basally it fractures, although the two halves remain in contact and function is unaffected. As in Spondylus, the halves of the anterior and posterior ligament layers unite on the two sides of the inner ligament layer. Owing to dorsal overgrowth by the hinge plate, the epithelia secreting the outer ligament layers form the two sides and roof of a chamber the base of which is the mantle isthmus (forming the inner ligament layer). Contact with the valves is exclusively by way of the outer ligament layers. The periostracum fuses in the mid-line dorsally and does not contribute to the ligament from which it is separated. Owing to the division of the inner ligament layer into right and left halves, union of the valves is effectively by way of the secondary teeth, here more dorsally extended than in Spondylus but, as there, composed of crossed-lamellar aragonite. Evolution of these four families starts in Palaeozoic stocks with modifications of organs in the mantle cavity - ctenidia, lips, pallial eyes, etc. - proceeding along lines distinct from those involving modifications in the ligament. The former particularly concern the primitive Propeamussidae, largely confined to deep water, and the universally distributed Pectinidae, the latter the Spondylidae and the Plicatulidae. Modifications of the foot have to do with final habit which is invariable freedom in the Propeamussidae, byssal attachment, freedom or cementation in the Pectinidae, and invariable cementation in the Spondylidae and Plicatulidae, the process occurring earlier in the latter and involving loss of the foot. Separation of the Spondylidae from the Pectinidae is more fully established with the present demonstration of the totally different ligamental structure; the difference is so profound in the Plicatulidae as to raise the question of elevating this to superfamily status.


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