Development of Turgida turgida (Rudolphi, 1819) (Nematoda: Physalopteroidea) in the opossum (Didelphis virginiana)

1982 ◽  
Vol 60 (6) ◽  
pp. 1265-1274 ◽  
Author(s):  
J. B. Gray ◽  
R. C. Anderson

Opossums given infective larvae of Turgida turgida were examined at various times after infection. Fifteen days after inoculation 13% of larvae recovered were undergoing the third moult. Thirty-five days after infection 20% of larvae found were moulting to the adult stage. The prepatent period was 89–105 days and the life span of worms was at least 360 days. The percentage of the inoculum recovered decreased with time. Also, development was asynchronous; i.e., third-, fourth-, and fifth-stage worms were found in individual opossums examined 40 and 160 days after infection. Second- and moulting second-stage larvae were not infective to opossums. Infections were successfully challenged. Attempts to infect cats (Felis catus), raccoons (Procyon lotor), and woodchucks (Marmota monax) were unsuccessful.

2019 ◽  
Vol 3 (1) ◽  
pp. 1
Author(s):  
Eny Coolfina Simarmata ◽  
Kusnoto Kusnoto ◽  
Mochamad Lazuardi ◽  
Setiawan Koesdarto ◽  
Endang Suprihati ◽  
...  

This study was aimed to identify the ultra structural morphology of Toxocara cati First Stage Larvae and Second Stage Larvae using Light Microscope. Toxocara cati larvae were obtained from adult worm eggs then were treated in phospat buffer saline with comparasion 1 : 1 until it reached the stage of larvae 1 and 2. The shell of egg Toxocara cati were thick and usually consist of three layers. The first layer was inner membrane, the second layer was middle layer and the third was outer layer. The results of larvae morphology that were identified using light microscope showed that the anterior part of Toxocara cati first stage larvae has a dorsal lip and esophagus and intestine on the posterior part but it could not be identified perfectly. The anterior part of Toxocara cati second stage larvae that were identified has three lips that leads directly into the oesophagus. Three lips on the anterior part of Toxocara cati larvae 2 consist of a dorsal lip and two subventral lips. Morphological of Toxocara cati larvae similar with the Toxocara cati adult worms because morphology of larvae and adult stage was difficult to differentiated.


1972 ◽  
Vol 50 (4) ◽  
pp. 437-450 ◽  
Author(s):  
Ronald C. Ko

Adults of Ackertia marmotae of groundhogs (Marmota monax) were located in lymphatics. Few microfilariae were recovered from blood but large numbers were in the reticular layer of the dermis, especially in skin of the ears. Microfilariae tended to accumulate in dermal tissue at feeding sites of Ixodes cookei.In laboratory-reared I. cookei maintained at 30C, microfilariae developed to the infective stage in about 1 month. First- and second-stage larvae were usually recovered from fat cells but some were also in epidermal cells. Infective larvae were found in the haemocoel and in ducts of salivary glands. Morphological changes of larvae during development are described; there is no "sausage-stage."One unfertilized female and one adult male A. marmotae were recovered from two groundhogs inoculated with infective larvae from laboratory-reared ticks. The prepatent period is estimated to be at least 1 year.Twenty-eight percent of 426 adult groundhogs examined in southern Ontario had adult worms. Microfilariae and adult worms were not found in 76 young of the year and 59 yearling animals.


1984 ◽  
Vol 62 (5) ◽  
pp. 965-979 ◽  
Author(s):  
Cheryl M. Bartlett

Development of Dirofilaria scapiceps (Leidy, 1886) was followed in 34 experimentally infected cottontail rabbits (Sylvilagus floridanus). Worms were recovered from all rabbits and intensity ranged from 8 to 76% of the number of infective larvae inoculated. Development to subadults occurred in subcutaneous tissues in various regions of the body; the specific region was influenced by the site of inoculation. The third and fourth moults occurred at 6 and 12 days postinoculation, respectively. Subadults migrated through the subcutaneous tissues and arrived in the ankles as early as 16 days postinoculation. Worms were sexually mature by 67 days. The prepatent period was 137–234 days and the microfilaraemia was nonperiodic. Few worms in cottontail rabbits degenerated or died and rabbits with 1-year-old infections could be reinfected. Dirofilaria scapiceps was recovered from 12 of 14 experimentally inoculated snowshoe hares (Lepus americanus) and 2 of 4 New Zealand white domestic rabbits (Oryctolagus cuniculus). Intensity in snowshoe hares and domestic rabbits ranged from 0.4 to 15% and 6 to 7%, respectively, of the number of infective larvae inoculated. Many worms in these hosts degenerated or died.


Ricercare ◽  
2020 ◽  
pp. 1-56
Author(s):  
Gilad Cohen

Firefly Elegy uses a 12-note melodic theme, which through the course of the piece undergoes a series of transformations - mirroring the metamorphosis that takes place over a firefly's brief life span. The piece comprises four sections that reflect the four life stages of the firefly. During the motionless egg stage, some types of fireflies glow dimly; the opening section of the piece (following a short fanfare of flashing-light) is likewise static and calm, while at the same time features an internal motion hinting at subdued energy. The following groovy section is at times aggressive, not unlike the firefly during its larva stage, when it is hunting and digesting insects using special enzymes. The firefly hibernates through the pupa stage - reflected in the third section of the piece by seemingly everlasting sustained chords in the strings. Like a flash of light, each new phrase begins with an ascending scale, while the harp provides groups of repeated notes, recalling the synchronized flashes that are found in groups of tropical fireflies. Firefly Elegy ends with an elegy in which the now mature firefly looks back at its life. It has gone through such an extensive journey but only long enough to mate and lay eggs, sometimes without feeding during its adult stage. In the summertime, I often watch the firefly in his lonely flutter, flashing about and looking for a mate so he can complete the sole purpose of his short life before dying away. He must sometimes look back and wonder: was it all worth it?


Parasitology ◽  
1963 ◽  
Vol 53 (1-2) ◽  
pp. 7-38 ◽  
Author(s):  
J. F. A. Sprent

The development ofAmplicaecum robertsihas been followed from the egg to the adult stage using laboratory mice and rats as intermediate hosts. The eggs were found to be resistant to desiccation and would develop under water; they were infective to mice after culturing for 18 days after removal from the uterus.Completion of the first moult occurred after hatching of the eggs in the intestine. Within 6 hr. of infection second-stage larvae had reached the liver. They also appeared in the lungs and carcass, but after 2 days were mostly confined to the liver.At 5–7 days after infection larvae underwent a period of lethargy followed by the second moult and the third-stage larvae commenced a period of growth reaching a length of 79 mm. at 28 weeks after infection in the liver of mice. In rats the growth of the larvae was slower for the first 2 months, but eventually they reached more or less the same proportions as in mice. The intestinal caecum appeared at a length of 3–4 mm., but there was no development of the reproductive organs throughout the third stage and no evidence of the third moult in rodents.Fifty carpet snakes were autopsied and searched for larvae and adults ofA. robertsi; in two snakes third-stage larvae were found in the aorta; in one snake the third moult was observed in the wall of the stomach and oesophagus; in three snakes the fourth moult was observed in the wall of the stomach; in twenty-six snakes adults were found.Experimental infection of laboratory-reared carpet snakes showed that infection with embryonated eggs resulted in second-stage larvae in the tissues which did not develop further. Infection with third-stage larvae, resulted in two distinct migratory patterns depending upon the maturity of the larvae administered. Larvae from the liver of laboratory rats which had been infected less than 12 weeks previously, migrated to various tissues, especially the aorta, of the snake, where they remained coiled in cysts filled with clotted blood for periods up to 112 days. Growth occurred within these cysts, but no evidence of moulting was observed. In contrast, larvae from the liver of laboratory rats infected 12 weeks or more previously, and from mice infected for 8 weeks or more, underwent the third moult in the wall of the oesophagus and stomach of the snake.With the onset of the fourth stage, the development of the reproductive organs became evident and continued during the fourth stage. It appeared that the fourth stage may occur in two phases, possibly depending on the size of the third-stage larva at the time of ingestion. Some experimental infections indicated that third-stage larvae may give rise to attached fourth stage larvae, probably capable of active growth. Other observations indicated that fourth-stage larvae may remain encapsulated in the wall of the stomach or oesophagus until sex differentiation is completed, after which the fourth moult occurs and the adult parasite emerges, leaving two sheaths of the same length within the capsule.The functional significance of each of the larval stages is discussed and it was concluded:—that the first-stage larva is one of tissue differentiation, whereby development proceeds to the infective stage; that the second stage represents a migratory phase without structural changes; that the third stage represents a growth phase, characterized by considerable increase in size, but without further radical changes in differentiation.In contrast, the fourth stage is characterized by absence of growth, inability to migrate, and by marked structural changes in the reproductive organs, whereby the sexes are differentiated. Evidently this development may take place while the fourth stage is attached to the wall of the stomach or oesophagus, or while the larva remains in the capsule in a state of quiescence.The fourth moult may occur in the attached state, but usually occurs within the capsule. After it is completed, the adult may remain for an indefinite period within the capsule with the two sheaths of the third and fourth stage. The emergence of the adult worms may be influenced by the arrival of food in the stomach. Once this phase is initiated, both growth and reproductive activity ensue during the adult stage.This work was financed by a research grant from the University of Queensland. The writer wishes to acknowledge the valuable assistance of Miss Ann Pritchard.


2015 ◽  
Vol 5 (3) ◽  
pp. 185-200
Author(s):  
Robert Z. Birdwell

Critics have argued that Elizabeth Gaskell's first novel, Mary Barton (1848), is split by a conflict between the modes of realism and romance. But the conflict does not render the novel incoherent, because Gaskell surpasses both modes through a utopian narrative that breaks with the conflict of form and gives coherence to the whole novel. Gaskell not only depicts what Thomas Carlyle called the ‘Condition of England’ in her work but also develops, through three stages, the utopia that will redeem this condition. The first stage is romantic nostalgia, a backward glance at Eden from the countryside surrounding Manchester. The second stage occurs in Manchester, as Gaskell mixes romance with a realistic mode, tracing a utopian drive toward death. The third stage is the utopian break with romantic and realistic accounts of the Condition of England and with the inadequate preceding conceptions of utopia. This third stage transforms narrative modes and figures a new mode of production.


2019 ◽  
Author(s):  
Lucy Armstrong ◽  
Lorna Hogg ◽  
Pamela Charlotte Jacobsen

The first stage of this project aims to identify assessment measures which include items on voice-hearing by way of a systematic review. The second stage is the development of a brief framework of categories of positive experiences of voice hearing, using a triangulated approach, drawing on views from both professionals and people with lived experience. The third stage will involve using the framework to identify any positve aspects of voice-hearing included in the voice hearing assessments identified in stage 1.


2018 ◽  
Vol 34 (02) ◽  
pp. 227-229
Author(s):  
Yi-gao Hu ◽  
Wei Ding ◽  
Jun Tan ◽  
Xin Chen ◽  
Tao Luo ◽  
...  

AbstractThis article investigates an effective method with which to reconstruct the tragus and external auditory meatus for microtia reconstruction. The external ear was reconstructed using a delayed postauricular skin flap in patients with congenital microtia. After the first stage of delaying the postauricular skin flap and the second stage of otoplasty with ear framework fabricated from autogenous rib cartilage draping with the delayed skin flap, the third stage involved tragus and external auditory meatus canaloplasty. After designing the remnant auricle flap, the lower part was trimmed and the tragus was reconstructed. The upper part was trimmed into a thin skin flap, which was rotated and used to cover the hollowed wound posterosuperior to the tragus so as to mimic the external auditory meatus. If remnant wounds were present, skin grafting was conducted. In total, 121 patients with congenital microtia were treated from March 2010 to March 2016. The reconstructed tragus and external auditory meatus were well formed, and all wounds healed well. No severe complications such as flap necrosis occurred. Six months postoperatively, the morphology of the reconstructed tragus and external auditory meatus was good. Overall, the patients and their families were satisfied. The use of remnant auricle to reconstruct the tragus and external auditory meatus is an effective auricular reconstruction technique.


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