The relationship between cirral activity and oxygen uptake in Balanus balanoides

1965 ◽  
Vol 45 (2) ◽  
pp. 387-403 ◽  
Author(s):  
R. C. Newell ◽  
H. R. Northcroft
Keyword(s):  
Body Weight ◽  
Oxygen Consumption ◽  
Oxygen Uptake ◽  
Mantle Cavity ◽  
The Body ◽  
Effect Of Temperature ◽  
Zero Rate ◽  
Rate Of Oxygen Consumption ◽  
The Relationship ◽  
Balanus Balanoides

The rate of cirral beat of Balanus balanoides is related to the logarithm of the body weight as an exponential function. In any one animal, there is little effect of temperature on cirral activity between 7·5° and 10° C. Between 10° and 20° C, however, there is a rapid increase in cirral beat with temperature followed by a fall at temperatures above 20° C.Balanus balanoides exhibits a fast, medium and zero rate of oxygen consumption. These rates of oxygen consumption correspond with (a) normal cirral beating, (b) ‘testing’ activity with no cirral movement, and (c) with the closure of the mantle cavity. Both of the possible levels of oxygen uptake are related to the logarithm of the body weight in a logarithmic fashion over the temperature range 7·5°–22·5° C. Temperature affects the two rates of oxygen consumption differently. In the slower rate (rate B) there is an increase in the rate of oxygen consumption between 7·5° and 14° C but there is no significant increase in the rate of oxygen consumption between 14° and 22·5 C°.

Heart rate as an indicator of oxygen consumption: influence of body condition in the king penguin

2001 ◽  
Vol 204 (12) ◽  
pp. 2133-2144 ◽  
Author(s):  
G. Froget ◽  
P. J. Butler ◽  
Y. Handrich ◽  
A. J. Woakes
Keyword(s):  
Heart Rate ◽  
Oxygen Consumption ◽  
Body Condition ◽  
Active Oxygen ◽  
The Body ◽  
Regression Equations ◽  
Oxygen Pulse ◽  
Rate Of Oxygen Consumption ◽  
The Impact ◽  
The Relationship

SUMMARY The use of heart rate to estimate field metabolic rate has become a more widely used technique. However, this method also has some limitations, among which is the possible impact that several variables such as sex, body condition (i.e. body fat stores) and/or inactivity might have on the relationship between heart rate and rate of oxygen consumption. In the present study, we investigate the extent to which body condition can affect the use of heart rate as an indicator of the rate of oxygen consumption. Twenty-two breeding king penguins (Aptenodytes patagonicus) were exercised on a variable-speed treadmill. These birds were allocated to four groups according to their sex and whether or not they had been fasting. Linear regression equations were used to describe the relationship between heart rate and the rate of oxygen consumption for each group. There were significant differences between the regression equations for the four groups. Good relationships were obtained between resting and active oxygen pulses and an index of the body condition of the birds. Validation experiments on six courting king penguins showed that the use of a combination of resting oxygen pulse and active oxygen pulse gave the best estimate of the rate of oxygen consumption V̇O2. The mean percentage error between predicted and measured V̇O2 was only +0.81% for the six birds. We conclude that heart rate can be used to estimate rate of oxygen consumption in free-ranging king penguins even over a small time scale (30min). However, (i) the type of activity of the bird must be known and (ii) the body condition of the bird must be accurately determined. More investigations on the impact of fasting and/or inactivity on this relationship are required to refine these estimates further.

scholarly journals Oxygen Consumption and Cell Size. A Comparison of the Rate of Oxygen Consumption of Diploid and Triploid Prepupae of Drosophila Melanogaster Meigen

1953 ◽  
Vol 30 (4) ◽  
pp. 475-491 ◽  
Author(s):  
C. ELLENBY
Keyword(s):  
Body Weight ◽  
Drosophila Melanogaster ◽  
Oxygen Consumption ◽  
Body Size ◽  
Surface Area ◽  
Cell Size ◽  
Rate Of Oxygen Consumption ◽  
The Mean ◽  
Relationship Of ◽  
The Relationship

1. The oxygen consumption and surface area of individual diploid and triploid prepupae of Drosophila melanogaster have been measured, the cells of triploid animals being larger. 2. The mean weights for the types examined are different but their ranges overlap almost completely. By covariance analysis it is shown that, after adjustment for difference in body size, there are no differences in the rates of oxygen consumption. It is concluded that, for these animals, cell size has no influence on the rate of oxygen consumption. 3. The relationships between body weight, surface area, and oxygen consumption have been further investigated. It is shown that, despite the greater inaccuracy of the method by which surface area is determined, oxygen consumption can be predicted more accurately from surface area than from body weight. 4. The results are discussed in relation to an earlier investigation of the oxygen consumption of other genotypes (Ellenby, 1945 a, b). Possible technical causes of certain differences between the two series of results in the relationship of oxygen consumption and body weight are explored; it is concluded, however, that they are almost certainly due to differences, not necessarily genetical, between the animals used in the two series.

Pulmonary function in different animals

1960 ◽  
Vol 15 (6) ◽  
pp. 1069-1072 ◽  
Author(s):  
James E. Drorbaugh
Keyword(s):  
Body Weight ◽  
Oxygen Consumption ◽  
Tidal Volume ◽  
Vital Capacity ◽  
Work Of Breathing ◽  
The Body ◽  
Small Animals ◽  
Similar Data ◽  
Body Weights ◽  
Rate Of Oxygen Consumption

Relaxation pressure-volume curves have been determined from the lungs and thorax of mice, rats, rabbits and dogs. From these data figures are obtained for body weights, vital capacity and compliance. These are compared with similar data for man and calculated values for tidal volumes and frequency of breathing obtained from the literature. Calculations were made of the elastic work of breathing per breath and per minute. All values were plotted on double log paper against body weight so that they could be expressed as proportional to some power of body weight. It was found that compliance, tidal volume, vital capacity and elastic work per breath are all nearly proportional to the first power of the body weight while the elastic work per minute, like the rate of oxygen consumption, is proportional to the 0.7 (or 0.73) power of body weight. It is concluded that lungs of large and small animals tend to have the same compliance per unit of vital capacity and require the same pressure for the intake of one tidal volume. A large lung may therefore be regarded as equivalent to many smaller lungs in parallel. Submitted on June 13, 1960

scholarly journals Body Size in Relation to Oxygen Consumption and Pleopod Beat in Ligia Oceanica L

1951 ◽  
Vol 28 (4) ◽  
pp. 492-507 ◽  
Author(s):  
C. ELLENBY
Keyword(s):  
Body Weight ◽  
Oxygen Consumption ◽  
Body Size ◽  
Body Length ◽  
Body Shape ◽  
Size Range ◽  
Total Oxygen ◽  
Rate Of Oxygen Consumption ◽  
Relationship Of ◽  
The Relationship

1. Male Ligia oceanica were used in an investigation of the relationship of body size to rate of oxygen consumption and pleopod beat. 2. Animals varied in weight from 0.04 to 1.03 g. and from 0.95 to 3.1 cm. in length. 3. Body shape does not change significantly over the size range, for length and breadth both increase at the same rate, and pleopod dimensions bear a constant relation to body length. 4. Specific gravity also is constant, for the relation of body weight to the cube of body length shows no trend with increasing size. 5. Oxygen consumption per gram decreases with increasing size and is proportional to the -0.274 Power of body weight. Total oxygen consumption is therefore proportional to the 0.726 power of body weight; but this value does not differ significantly from two-thirds. 6. As shape is constant, surface area is proportional to the square of a linear dimension. It is shown that oxygen consumption per unit of length2 is constant over the size range. Although body length was measured far less accurately than body weight it is shown that it assesses ‘body size’ more accurately. 7. Rate of pleopod beat was measured at 15 and 25°C.; it decreases with the size of the animal. At 15°C. time per beat varies as the 0.66 power of body length, and at 25°C. as the 0.59 power; neither of these values differs significantly from 0.5. Despite the fact that pleopod movement is heavily damped, the rate therefore varies like that of a pendulum. 9. The workof Fox (1936-9) and Fox et al. (1937a)on the rate of oxygen consumption of animals from cold and warmer seas and from different habitats is considered. It is suggested that many of their comparisons are invalidated by differences in body size of the animals concerned, and that, in relation to environment, no basis, theoretical or experimental, has been established for a distinction between ‘nonlocomotory’ and ‘activity’ metabolism.

scholarly journals The Respiration of some Planktonic copepods II. The Effect Of Temperature

1953 ◽  
Vol 31 (3) ◽  
pp. 447-460 ◽  
Author(s):  
D. T. Gauld ◽  
J. E. G. Raymont
Keyword(s):  
Respiratory Rate ◽  
The Body ◽  
The Other ◽  
Effect Of Temperature ◽  
Acartia Clausi ◽  
Temora Longicornis ◽  
Different Temperatures ◽  
Planktonic Copepods ◽  
The Difference ◽  
The Relationship

The respiratory rates of three species of planktonic copepods, Acartia clausi, Centropages hamatus and Temora longicornis, were measured at four different temperatures.The relationship between respiratory rate and temperature was found to be similar to that previously found for Calanus, although the slope of the curves differed in the different species.The observations on Centropages at 13 and 170 C. can be divided into two groups and it is suggested that the differences are due to the use of copepods from two different generations.The relationship between the respiratory rates and lengths of Acartia and Centropages agreed very well with that previously found for other species. That for Temora was rather different: the difference is probably due to the distinct difference in the shape of the body of Temora from those of the other species.The application of these measurements to estimates of the food requirements of the copepods is discussed.

The Oxygen Consumption of an Echiuroid, Bonellia Viridis Rolando

1968 ◽  
Vol 48 (2) ◽  
pp. 427-434
Author(s):  
A. E. BRAFIELD
Keyword(s):  
Oxygen Consumption ◽  
Body Size ◽  
Continuous Flow ◽  
Muscular Activity ◽  
Dry Weight ◽  
The Body ◽  
Body Region ◽  
Rate Of Oxygen Consumption

1. The oxygen consumption of the echiuroid Bonellia viridis has been investigated by means of a continuous-flow polarographic respirometer. 2. The general rate of oxygen consumption per unit dry weight is similar to that characteristic of polychaetes, and declines exponentially with increasing body size. 3. The rate of oxygen consumption rises in the light and falls again if darkness is restored. 4. The oxygen consumption of the isolated proboscis plus that of the isolated body region corresponds closely to that of the entire animal. 5. The oxygen consumption per unit dry weight of the proboscis is considerably higher than that of the body region. 6. The oxygen consumption of an isolated body region increases in the presence of light, but that of an isolated proboscis does not. 7. These findings are discussed in relation to the biology of the animal, observed muscular activity, and the occurrence of the pigment bonellin.

The development of the lamb with particular reference to the alimentary tract

1964 ◽  
Vol 6 (2) ◽  
pp. 169-178 ◽  
Author(s):  
R. V. Large
Keyword(s):  
Body Weight ◽  
Alimentary Tract ◽  
Live Weight ◽  
The Body ◽  
Root Transformation ◽  
Feeding Regimes ◽  
Gut Fill ◽  
Relationship Of ◽  
The Relationship

1. Thirty Suffolk × Half bred lambs were slaughtered at the following ages: two twin lambs at birth and two singles and two twins at 1, 2, 3, 4, 6, 8 and 16 weeks of age.2. The following weights were recorded: live-weight immediately before slaughter; and carcass, head, skin, feet, alimentary tract, heart, liver, kidneys, lungs and trachea, and blood immediately afterwards.3. The alimentary tract was emptied and weighed in four separate parts; reticulo-rumen, omasum-abomasum, small intestine, large intestine.4. The volumes of the reticulo-rumen and the omasum-abomasum were measured by immersing in water and filling the organs with water to 2 cm. pressure.5. The in vitro digestive efficiency of rumen liquor from lambs of 1, 2, 3 and 4 weeks of age was assessed.6. Empty body weight was considered to be valuable in comparing animals of different ages or from different feeding regimes or at different times of the year because variations in gut ‘fill’ were eliminated.7. There were no differences between singles and twins in the relationship of the fresh weights of the parts of the body to empty body weight, except that development of the liver and the blood was rather slower for singles.8. Little evidence was found of a difference in rate of development of the alimentary tract between singles an d twins, although the log an d square root transformation suggested a possible difference in reticulo-rumen size in favour of twins, significant at the 5% level.

scholarly journals The relationship between body weight and exterior measurements in domestic ostriches during the first four months after hatching

2007 ◽  
Vol 23 (1-2) ◽  
pp. 13-20
Author(s):  
Andrey Kurtenkov
Keyword(s):  
Body Weight ◽  
Detailed Analysis ◽  
The Body ◽  
The Other ◽  
Phenotypic Correlation ◽  
Other Hand ◽  
The One ◽  
The Relationship ◽  
Selection Of

It is related leg problems to the realization of the necessity of doing a detailed analysis of the phenotype correlations between body weight and exterior measurements. As a result of the study, lower coefficients have been obtained of the correlation between the girth of the tarso metatarsus on one hand, and the body weight and the girth behind the wings, on the other hand (respectively 0.563 and 0.608), compared with the one between the body weight and the girth behind the wings (0.898). It is advisable in the selection of ostriches to take into consideration the necessity of a higher phenotypic correlation between the girth of the tarso metatarsus on the one hand, and the body weight and the girth behind the wings on the other hand, with a view to preventing leg problems.

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