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Biomedical subjects

K Schmidt-Nielsen

Publications and source records attributed to K Schmidt-Nielsen.

At least 37 records · Page 2Linked to original sources

Effect of arterial carbon dioxide on cerebral blood flow in ducks.

The purpose of this study was to determine the effect of arterial PCO2 on blood flow to the avian brain. Cerebral blood flow was measured on curarized, artificially ventilated Pekin ducks by the rate at which intra-arterially injected xenon-133 was cleared from the duck's brain. A two-component clearance curve resulted: the blood flow calculated from the fast and slow components was similar to the blood flow to mammalian grey and white matter, respectively. Hypercapnia markedly increased the fast component of blood flow, whereas hypocapnia had no effect on this component. These effects were not due to changes in blood pressure, which was independent of arterial PCO2. Blood flow calculated from the slow component was independent of arterial PCO2. We conclude that the lack of response to hypocapnia may contribute to the exceptional tolerance of birds to high altitude by maintaining normal cerebral blood flow.

Animals↗

Heat loss from feet of herring gulls at rest and during flight.

The role of the feet of herring gulls (Larus argentatus) in heat dissipation was estimated during rest and wind-tunnel flight. We determined the blood flow to the feet and the arteriovenous temperature difference and thus estimated heat loss from the feet. Determinations of oxygen consumption and respiratory water loss at rest gave a heat production of about 8 W; 37-56% of this heat was lost from the feet (air temp = 10-35 degrees C). During flight heat production was estimated to be about 57 W and heat loss from the feet was 46 W, about 80% of the heat production in flight. Thus the webbed feet are an important avenue of heat loss in the herring gull.

Animals↗

Energy expenditure for thermoregulation and locomotion in emperor penguins.

During the antarctic winter emperor penguins (Aptenodytes forsteri) spend up to four mo fasting while they breed at rookeries 80 km or more from the sea, huddling close together in the cold. This breeding cycle makes exceptional demands on their energy reserves, and we therefore studied their thermoregulation and locomotion. Rates of metabolism were measured in five birds (mean body mass, 23.37 kg) at ambient temperatures ranging from 25 to -47 degrees C. Between 20 and -10 degrees C the metabolic rate (standard metabolic rate (SMR)) remained neraly constant, about 42.9 W. Below -10 degrees C metabolic rate increased lineraly with decreasing ambient temperature and at -47 degrees C it was 70% above the SMR. Mean thermal conductance below -10 degrees C was 1.57 W m-2 degrees C-1. Metabolic rate during treadmill walking increased linearly with increasing speed. Our data suggest that walking 200 km (from the sea to the rookery and back) requires less than 15% of the energy reserves of a breeding male emperor penguin initially weighing 35 kg. The high energy requirement for thermoregulation (about 85%) would, in the absence of huddling, probably exceed the total energy reserves.

Animals↗

Scaling in biology: the consequences of size.

A review of major ideas pertaining to the importance of the body size of animals. It discusses the size range of living organisms and the possibilities and constraints that result from the design of animals and the materials used in their supporting structures. The change in size of similarly organized animals is considered in the light of the principles of scaling, with examples chosen both from morphology and physiology. The mechanical consequences of body size in relation to locomotion is also discussed.

Animals↗

A model of respiratory heat transfer in a small mammal.

A steady-state model of the heat and water transfer occurring in the upper respiratory tract of the kangaroo rat, Dipodomys spectabilis, is developed and tested. The model is described by a steady-state energy balance equation in which the rate of energy transfer from a liquid stream (representing the flow of heat and blood from the body core to the nasal region) is equated with the rate of energy transfer by thermal conduction from the nose tip to the environment. All of the variables in the equation except the flow rate of the liquid stream can be either measured directly or estimated from physiological measurements, permitting the solution of the equation for the liquid stream flow rate. After solving for the liquid stream flow rate by using data from three animals, the energy balance equation is used to compute values of energy transfer, expired air temperature, rates of water loss, and efficiency of vapor recovery for a variety of ambient conditions. These computed values are compared with values measured or estimated from physiological measurements on the same three animals, and the equation is thus shown to be internally consistent. To evaluate the model's predictive value, calculated expired air temperatures are compared with measured expired air temperatures of eight additional animals. Finally, the model is used to examine the general dependence of expired air temperature, of rates of water loss, and of efficiency of vapor recovery on ambient conditions.

Animals↗