Early Stages of Some Copepods (Crustacea) Parasitic on Marine Fishes of British Columbia

1976 ◽  
Vol 33 (11) ◽  
pp. 2507-2525 ◽  
Author(s):  
Z. Kabata

Detailed descriptions and illustrations are presented of the nauplii (the only, or the first nauplius stage) of Bomolochus cuneatus, Holobomolochus spinulus, Chondracanthus gracilis, Ergasilus turgidus, Eudactylina similis, Pseudocharopinus dentatus, and Haemobaphes diceraus, and the copepodid stages of H. diceraus, P. dentatus, and Nectobrachia indivisa.The naupliar morphology of Ergasilus is similar to that of free-living Cyclopidae but differs in significant details from that of supposedly related Bomolochus. The nauplii of poecilostome and siphonostome copepods are similar. The morphology of the free-living larval stages might offer valuable clues to intrafamilial relationships of Lemaeopodidae. Differences were observed between copepodids of two species of Haemobaphes.

2001 ◽  
Vol 31 (5) ◽  
pp. 839-842 ◽  
Author(s):  
Clóvis de Paula Santos ◽  
Terezinha Padilha ◽  
Maria de Lurdes de Azevedo Rodrigues

The effect of different temperatures on the predatory activity of Arthrobotrys oligospora and Duddingtonia flagrans on the free-living larval stages of cyathostomes were evaluated in an experiment where feces of horses containing the parasites’ eggs were treated with these fungi and incubated under different constant temperatures (10°C, 15°C, 20°C, 25°C and 30°C ). The results indicated that the optimum temperature for egg development was 25°C. At 10°C the number of L3 recovered was practically zero, and at 15°C and 20°C, the percentage of larvae recovered was less than 3% of the total number of eggs per gram of feces. When these cultures subsequently were incubated for an additional period of 14 days at 27°C, they allowed the development of L3. In all the cultures inoculated with fungi a significant reduction in the number of larvae was observed. When incubated at 25°C or 30°C, the fungi caused reductions above 90%, in the number of L3. The samples cultivated at 10°C, 15°C, 20°C, 25°C and 30°C, when incubated for an additional period of 14 days at 27°C the reduction percentage of larvae was above 90% for A. oligospora. However, the same did not occur for D. flagrans. Here a reduction percentage between 47.5% and 41.8% was recorded when the cultures were incubated at 10°C and 20°C, respectively. The two species of fungi tested showed to be efficient in reducing the number of L3 when mixed with equine feces and maintained at the same temperature for the development of larval pre-parasitic stages of cyathostomes.


Author(s):  
Jan A. Pechenik

I have a Hardin cartoon on my office door. It shows a series of animals thinking about the meaning of life. In sequence, we see a lobe-finned fish, a salamander, a lizard, and a monkey, all thinking, “Eat, survive, reproduce; eat, survive, reproduce.” Then comes man: “What's it all about?” he wonders. Organisms live to reproduce. The ultimate selective pressure on any organism is to survive long enough and well enough to pass genetic material to a next generation that will also be successful in reproducing. In this sense, then, every morphological, physiological, biochemical, or behavioral adaptation contributes to reproductive success, making the field of life cycle evolution a very broad one indeed. Key components include mode of sexuality, age and size at first reproduction (Roff, this volume), number of reproductive episodes in a lifetime, offspring size (Messina and Fox, this volume), fecundity, the extent to which parents protect their offspring and how that protection is achieved, source of nutrition during development, survival to maturity, the consequences of shifts in any of these components, and the underlying mechanisms responsible for such shifts. Many of these issues are dealt with in other chapters. Here I focus exclusively on animals, and on a particularly widespread sort of life cycle that includes at least two ecologically distinct free-living stages. Such “complex life cycles” (Istock 1967) are especially common among amphibians and fishes (Hall and Wake 1999), and within most invertebrate groups, including insects (Gilbert and Frieden 1981), crustaceans, bivalves, gastropods, polychaete worms, echinoderms, bryozoans, and corals and other cnidarians (Thorson 1950). In such life cycles, the juvenile or adult stage is reached by metamorphosing from a preceding, free-living larval stage. In many species, metamorphosis involves a veritable revolution in morphology, ecology, behavior, and physiology, sometimes taking place in as little as a few minutes or a few hours. In addition to the issues already mentioned, key components of such complex life cycles include the timing of metamorphosis (i.e., when it occurs), the size at which larvae metamorphose, and the consequences of metamorphosing at particular times or at particular sizes. The potential advantages of including larval stages in the life history have been much discussed.


2019 ◽  
Vol 94 ◽  
Author(s):  
Y. Kuzmin ◽  
V.V. Tkach ◽  
F.T.V. Melo

Abstract Serpentirhabdias mussuranae n. sp. is described from the lungs of the mussurana, Clelia clelia (Daudin, 1803), from vicinities of Lábrea, Amazonas State, Brazil. The species is characterized by the triangular oral opening, the presence of teeth (onchia) in the oesophastome, the excretory glands longer than the oesophagus and the tail abruptly narrowing in its anterior half and gradually tapering in posterior half. Among the Neotropical representatives of the genus, three species are known to possess the onchia in the oesophastome: S. atroxi, S. moi and S. viperidicus. Serpentirhabdias mussuranae n. sp. differs from S. atroxi and S. viperidicus by its triangular shape of the oral opening and the oesophastome in apical view, vs. round in the latter two congeners. Additionally, S. viperidicus has a larger oesophastome, 13–22 micrometers wide and 13–23 micrometers deep. The new species has relatively longer excretory glands than S. moi. The new species is morphologically and genetically close to S. atroxi, S. moi and S. viperidicus, all parasitic in Brazilian snakes, based on the presence of onchia and the comparison of nucleotide sequences of nuclear ribosomal DNA and mitochondrial cox1 gene (differences varied between 3.8% and 7.1%). Data on the life cycle of S. mussuranae n. sp. is provided, and the life cycle is typical of the genus Serpentirhabdias, with the combination of direct development and heterogony. Free-living larval stages and the adults of amphimictic free-living generation are described. The results of molecular phylogenetic analysis based on nuclear ribosomal internal transcribed spacer (ITS) + partial 28S region and partial mitochondrial cox1 gene are provided.


2010 ◽  
Vol 79 (2) ◽  
pp. 79-84 ◽  
Author(s):  
Junzeng Xue ◽  
Yan Liu ◽  
Neil Cumberlidge ◽  
Huixian Wu

This paper focuses on the developmental changes that take place inside the eggs of the semi-terrestrial freshwater crab, Sinopotamon yangtsekiense, from Qiantang River in Zhejiang Province, China. The egg consists of two layers, a thick outer membrane and a thin inner membrane that encloses the fluidfilled embryonic sac. Development in this species took up to 77 days, after which the free-living juvenile hatchling crab emerged from the egg. During development the embryo underwent a series of morphological changes that corresponded to the free-living larval stages of marine crabs, and the yolk mass decreased in size and changed color (from creamy pale yellow, to orange, and finally grey). The eggs remained attached to the pleopods in the female’s abdominal brood pouch during development and showed a great deal of independence from water. Embryos developed normally whether they were immersed in water or in air. The implications of this adaptation for freshwater crab evolution are discussed.


Parasitology ◽  
1968 ◽  
Vol 58 (3) ◽  
pp. 641-651 ◽  
Author(s):  
J. Barrett

The development of the free-living infective larvae of a homogonic strain Strongyloides ratti is described.The larvae develop only between 15 and 34 °C. Transfer experiments show the temperature block to be in the preparation for the second moult.Within the temperature range 15–34 °C, increasing the temperature speeds up the rate of development of all the larval stages equally, the Q10 for development being 2·5.The maximum percentage development occurs at 20 °C. The percentage development is highest in faeces–peat culture (95% development at 20 °C), whilst the percentage development in charcoal and vermiculite cultures is about the same (75% development at 20 °C.).Larvae grown on charcoal cultures are larger than those grown on vermiculite, which are larger than those grown on peat. No significant difference was found in the length:oesophagus and length:width ratios or in the variability of larvae grown at different temperatures or on different culture media.Different worm densities in the cultures of from 2000 to 10000 larvae per g of culture did not affect either the size of the infective larve or the percentage development.The optimum temperature for survival is 15 °C. Worms grown at 20 °C lived longer than worms grown at any other temperature. There was no evidence of temperature adaptation by the larvae.The infective larvae are positively thermotactic, and show maximum activity at 37 °C.I should like to thank my supervisor, Dr Tate, for his advice and encouragement. The work was carried out during the tenure of a Medical Research Council Scholarship.


2001 ◽  
Vol 79 (7) ◽  
pp. 1125-1170 ◽  
Author(s):  
Larry R McEdward ◽  
Benjamin G Miner

We review the literature on larval development of 182 asteroids, 20 crinoids, 177 echinoids, 69 holothuroids, and 67 ophiuroids. For each class, we describe the various larval types, common features of a larval body plan, developmental patterns in terms of life-cycle character states and sequences of larval stages, phylogenetic distribution of these traits, and infer evolutionary transitions that account for the documented diversity. Asteroids, echinoids, holothuroids, and ophiuroids, but not crinoids, have feeding larvae. All five classes have evolved nonfeeding larvae. Direct development has been documented in asteroids, echinoids, and ophiuroids. Facultative planktotrophy has been documented only in echinoids. It is surprising that benthic, free-living, feeding larvae have not been reported in echinoderms. From this review, we conclude that it is the ecological and functional demands on larvae which impose limits on developmental evolution and determine the associations of larval types and life-cycle character states that give rise to the developmental patterns that we observe in echinoderms. Two factors seriously limit analyses of larval and life-cycle evolution in echinoderms. First is the limited understanding of developmental diversity and second is the lack of good phylogenies.


Author(s):  
Thomas Bartolomaeus

It is generally believed that lecithotrophic larvae of annelids do not possess functional excretory organs. However, as in certain annelids the planktotrophic trochophora larva has been secondarily modified into a lecithotrophic developmental stage and because protonephridia are characteristic for the trochophora, lecithotrophic developmental stages should also possess such organs. To test this assumption hatchlings of the orbiniidan Scoloplos armiger, which develops directly without a free-living larval stage, were investigated ultrastrucrurally. Each hatchling possesses a pair of protonephridia which lie caudal to the eyes and almost level with the frontal margin of the foregut. Each organ consists of three multiciliated cells, a terminal cell, a duct cell and a nephropore cell. The terminal cell bears a distally oriented hollow cytoplasmic cylinder, which surrounds the cilia. Adherens junctions connect this structure to the duct cell. Several clefts and pores perforate the wall of the hollow cylinder. Extracellular material covers the pores and clefts and thus may function as a molecular sieve during filtration. A comparison with the protonephridia of other annelid larvae reveals: (1) that one pair of protonephridial head kidneys consisting of a terminal cell, a duct cell and a nephropore cell must be assumed for the trochophore in the ground pattern of annelids and (2) that these organs are preserved when lecithotrophic larval stages evolved within the Annelida


Parasitology ◽  
1964 ◽  
Vol 54 (1) ◽  
pp. 1-41 ◽  
Author(s):  
B. L. James

1. Parvatrema homoeotecnum sp.nov. from the oystercatcher, Haematopus ostralegus occidentalis Neumann at Aberystwyth is described and compared with other species of the genus.2. The life cycle of this species is unique. The larval stages occur in the gastropod, Littorina saxatilis (Olivi) subsp. tenebrosa (Montagu) and include germinal sacs which have a structure and development similar to an adult digenean. There are no free-living stages and only one intermediate host.3. The significance of this unique life cycle is discussed.4. The family Gymnophallidae Morozov, 1955, is reviewed. Emended definitions are given for the family, subfamilies and genera. Keys, diagnostic features and brief notes of the species are included.I am very grateful to Dr Gwendolen Rees, who suggested the investigation which led to the discovery of this species, for her advice and indispensable assistance throughout the work and the preparation of this paper. I am also grateful to the late Professor T. A. Stephenson for his interest and for the provision of working facilities; to Mr W. A. Ballantine, Mr A. H. Clarke, Jr., Mr C. Curtis, Miss G. P. F. Evans, Dr V. Fretter, Professor L. A. Harvey, Mr D. H. Jones and Dr J. Lewis who sent me specimens of Littorina saxatilis; to Professor R. M. Cable and Emerit. Professor G. R. La Rue for helpful suggestions; to Mr J. R. Hirst and Mr D. Hemingway Jones for photographic and technical assistance and to the Department of Scientific and Industrial Research for a grant which made the work possible.


1923 ◽  
Vol 1 (1) ◽  
pp. 21-28 ◽  
Author(s):  
A.J. Hesse

The only account of the larval stages of Bunostomum trigonocephalum (Rud.) which I have been able to find is a brief note by Baillet (1866), in which he states that the larvæ of Uncinaria cernua Crep. = B. trigonocephalum (Rud.), develop in water and hatch within four or six days. The newly hatched larvæ are “rhabditiform,” .35 to .4 mm. long and ·23 to .3 mm. broad, and the tail is very thin and filiform.


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