Growth and respiration throughout the life-cycle of Nematospiroides dubius Baylis, 1926 (Nematoda: Heligmosomidae)

Parasitology ◽  
1973 ◽  
Vol 67 (3) ◽  
pp. 245-251 ◽  
Author(s):  
Victoria Bryant

The growth of the three free-living stages of N. dubius was measured in terms of dry and fresh weight. Changes in body water content during moulting were demonstrated by variations in dry weight when expressed as a percentage of fresh weight. The respiration rate of the larvae increased until they became infective, after which time it decreased until five days later no oxygen consumption could be recorded. The inability of all larval stages to withstand anaerobic conditions indicated that their metabolism was essentially aerobic. The relationship between body size and metabolic rate was established for each stage and its significance in relation to the life-cycle discussed.

Parasitology ◽  
1974 ◽  
Vol 69 (1) ◽  
pp. 97-106 ◽  
Author(s):  
Victoria Bryant

The growth of male and female parasitic stages of Nematospiroides dubius from male and female ASH/CS1 mice was measured in terms of dry weight. No sex-linked resistance of mice to infection with N. dubius was apparent, as growth was the same in both sexes of host. The growth rate did not alter when moulting occurred.All parasitic stages of N. dubius consumed oxygen in vitro and oxygen was also shown to be necessary for motility and survival.The relationship between body size and metabolic rate was established for male and female parasitic N. dubius and the b values indicated that aerobic metabolism is of functional importance to this species.The size/metabolism relationship for the whole life-cycle was established.


1982 ◽  
Vol 60 (8) ◽  
pp. 1945-1950 ◽  
Author(s):  
Thierry Pilorge

The diet of Lacerta vivipara was estimated in the laboratory by determining the relationship between fecal production and food intake. Transposed to free-living individuals, this relationship between the daily consumption C in milligrams of dry weight and the total fresh weight of lizards in grams becomes C = 20.4 W0,85. By knowing the number of days during which lizards can eat, the assimilation rate, the weight increase, the mean weight of the tail, the rate of autotomy, and the weight of a brood, the individual energy budget has been established for each sex according to age. The proportion of the assimilated biomass used for growth reaches a peak in young lizards, then decreases regularly to a negligible degree in older animals. The energy used for reproduction is low at first in primiparous females but becomes three times as great in older females.[Traduit par le journal]


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.


Author(s):  
G. M. Hughes ◽  
N. K. Al-Kadhomiy

Relationships between respiratory area, oxygen consumption, and body mass have been examined during the development of water- and air-breathing fish. It is concluded that there is at least one stage at which the slope of the relationship between log gill area and log body weight changes during fish development. This usually occurs in the weight range 0.05–1.0 g and is often associated with a distinct metamorphosis, but no common functional significance can be attached to them. However, the change in slope does not appear to be associated with a comparable inflexion in the corresponding relationship between body mass and oxygen consumption (routine). It seems probable that other surfaces are important during these transitions and that the total gas-exchange surface of the fish shows a more constant change throughout the life history. Further analyses of a wider range of species is required to test this hypothesis.


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.


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.


2002 ◽  
Vol 76 (3) ◽  
pp. 189-192 ◽  
Author(s):  
F. Audebert ◽  
H. Hoste ◽  
M.C. Durette-Desset

AbstractThe chronology of the life cycle ofTrichostrongylus retortaeformis(Zeder, 1800) (Nematoda, Trichostrongyloidea) is studied in its natural hostOryctolagus cuniculus. The free living period lasted 5 days at 24°C. Worm-free rabbits were each infectedper oswithT. retortaeformislarvae. Rabbits were killed at 12 h post-infection (p.i.) and every day from one day to 13 days p.i. By 12 h p.i., all the larvae were exsheathed and in the small intestine. The third moult occurred between 3 and 5 days p.i. and the last moult between 4 and 7 days p.i. The prepatent period lasted 12 to 13 days. The patent period lasted five and a half months. The four known life cycles of species ofTrichostrongylusin ruminants were compared with that ofT. retortaeformis. No significant difference was found except in the duration of the prepatent period. These similarities in the life cycles confirm the previously formulated hypotheses on the relationship between the parasites of the two host groups ().


1973 ◽  
Vol 59 (1) ◽  
pp. 255-266
Author(s):  
H. J. ATKINSON

1. The rate of oxygen consumption of individual males of Enoplus brevis and E. communis was measured at 15 °C and at each of four oxygen tensions, 135, 75, 35, and 12 Torr, after at least 12 h experience of these conditions. 2. It was clearly demonstrated that the level of oxygen consumption of both species was reduced by each lowering of the imposed oxygen tension. 3. In all cases the oxygen consumption of each species fell with increasing body size. On a unit dry-weight basis the oxygen consumption of E. brevis is greater than that of the larger E. communis, but after allowing for the difference of body size the two species have more or less similar oxygen uptakes at all oxygen tensions. 4. In E. brevis oxygen tension influenced the relationship of body size and metabolism, the slope relating oxygen consumption and body weight becomes steeper with decreasing oxygen tension. This effect was not shown by E. communis. 5. Some general factors influencing the availability of oxygen to nematodes are considered.


2004 ◽  
Vol 82 (10) ◽  
pp. 1655-1666 ◽  
Author(s):  
A Baud ◽  
C Cuoc ◽  
J Grey ◽  
R Chappaz ◽  
V Alekseev

The gut structure and ultrastructure of Neoergasilus japonicus (Harada, 1930), a copepod from the family Ergasilidae (Copepoda, Poecilostomatoida) and a parasite of fish, were compared at different periods of the life cycle: in free-living specimens in October and after attaching to fish in January and June. Differences in the depth of the intestinal epithelium were prominent and other cellular characteristics appeared seasonally variable. We relate these to changes in the physiological activity. Preliminary data from stable-isotope analyses of attached specimens suggest nutritional contribution from parasitism. The possibility of a diapause in the life cycle, as well as the relationship between the morphology of the gut and early evolutionary parasitism of N. japonicus, are discussed.


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