(Received 10 June 1950)

Size: px
Start display at page:

Download "(Received 10 June 1950)"

Transcription

1 459 J. Physiol. (I95I) II2, THE LOSS OF HEAT FROM THE HANDS AND FROM THE FINGERS IMMERSED IN COLD WATER BY A. D. M. GREENFIELD, J. T. SHEPHERD AND R. F. WHELAN From the Department of Physiology, The Queen's University of Belfast (Received 10 June 1950) The calorimetric method has recently been applied (Greenfield & Shepherd, 1950) to the study of the vasodilatation induced in the finger tip by immersion in cold water (Lewis, 1930). In the course of these observations it was found that the heat loss from the terminal 2X8 cm. of the index finger (hereafter called the finger tip) immersed in water at 0-6 C. varied in different subjects from 1100 to 3400 small calories (cal.)/100ml. of tissue/min. at the height of cold vasodilatation. During the first hour of immersion the total heat loss was as much as 3X8 large calories (kg.cal.). If, when the whole hand is immersed, the heat loss were proportional to that from the finger tip, it would in some persons amount to as much as 840 kg.cal./hr. However, there are reasons, considered later, for expecting the heat loss from the whole hand to be proportionately less than that from a single finger tip. The experiments now described show that this is in fact the case. Observations have been made on the heat loss from the whole hand, and also from the four fingers. METHODS The calorimeters used were of the vacuum jar type described by Greenfield & Scarborough (1949). The calorimeter employed in the 06 C. range had the electric heating coil disconnected; that employed in the C. range had the coil in operation. In experiments where the whole hand was observed no other modifications were made. When the fingers onlv were observed, a transverse shelf was arranged 9 cm. below the under surface of the lid of the calorimeter (Fig. 1). A post, 8 cm. high, was erected on this shelf. The calorimeter was filled to the top of the post, a volume equal to that of the fingers to be immersed was removed, and the fingers inserted until- the tip of the middle one rested on the shelf. The position of this finger tip on the shelf was maintained by a wire ring. When the fingers were in cold water and sensation numbed, this ring prevented the finger slipping off the shelf. The temperature of the calorimeter contents, registered by a thermo meter graduated in hundredths of a degree C., was recorded at intervals of 1 min. On the scale 10 C. measured 7-5 cm., and an attempt was made to estimate the temperature to a thousandth of a degree Centigrade. Observations of the heating rate of the calorimeter showed that our readings agreed within ±2 milli C. of the average rate. It was only necessary to measure differences of temperature with great accuracy. The actual temperatures could not, of course, be measured with comparable confidence.

2 460 A. D. M. GREENFIELD, J. T. SHEPHERD AND R. F. WHELAN Measurement of volumes offingers and hand. The volume of the fingers was measured by inserting them into a narrow oval vessel until the middle finger touched the bottom. The vessel was then filled to a depth of 8 cm., the fingers removed and the volume of water needed to restore the depth to 8 cm. was measured. The volume of the hand was measured by the method of Greenfield & Scarborough (1949). This method is accurate to ± 10 ml. (McCorry, 1950). Wall of Shelf Ring for 'thermos' suspended from finger tip jar top of jar Fig. 1. A section through the top of the calorimeter to show the four fingers in position, the middle finger resting on a shelf 8 cm. below the water level. The thermometer and stirrer are not shown. Mea8urement of the surface area of immersed tissue. Two methods were used: (a) A comfortably fitting rubber glove was marked at the various levels of immersion. It was then cut up and the parts which had been immersed were weighed. These weights were then compared with the weight of a known area from the same glove. The weights of equal areas from different parts of the glove agreed to within 5 %. (b) Adhesive plaster was carefully applied, and while in position marked at the various levels of immersion. It was then removed, cut up, and the parts weighed. A measured area of the same plaster was also weighed. In both cases areas were deduced from the weight of material.

3 HEAT LOSS FROM THE HAND 461 RESULTS Heat loss from the hands to water at 0-60 C. The standard procedure was to immerse the hand in a water-bath at 290 C. for at least 20 min. and then to dry it and transfer it to a calorimeter, the contents of which were at about 10 C. The other hand was similarly treated, but was inserted about 5 min. earlier into another calorimeter containing water at about 290 C. The measurements on this hand indicated the general level of vasomotor tone. Heat lossfrom a hand with the circulation arrested. The immersion of a hand with the circulation arrested in water at about 10 C. is extremely painful, and observations were made on two occasions only. The results of one of these experiments in which the subject kept his hand in the water for 11 min. are shown in Table 1. The rate of heat loss had fallen in the 8th min. to less than one-tenth of its value in the 1st min. The heating rate of the calorimeter was 12 milli C./min. in the period before immersion of the hand (Table 2, column 3). A constant correction of -12 milli' C. has been applied to the remaining figures in the column to obtain the temperature rise due to the immersed hand (column 4). No serious error is involved in assuming a constant heating correction. The results of this experiment, which are similar to those of the other comparable experiment, have been employed to arrive at the heat loss from the circulating blood in the main series of experiments. There are five difficulties in so employing these results: (1) Although the hands in this and in the other experiments were equilibrated with water at 29 C. for at least 20 mm., it is unlikely that at the end of this time the internal temperature of the hands was 290 C. (Barcroft & Edholm, 1943). It cannot even be assumed that the internal temperature was the same on different occasions, as it must have depended on the state of the circulation at the time. (2) Results obtained in this way on one person may not in fact be strictly applicable to other persons' hands. It is thought unlikely, however, that the thermal conductivities and specific heats of different hands vary enough to make this objection important. (3) No figures are available after the 11th min. when the heat output from the hand with the circulation arrested was 31 cal./100 ml./min. We have assumed that the heat loss continued at this rate, although in fact it must have fallen further. (4) In our calculations it is assumed that the hand cools to the calorimeter temperature. In fact it does not do so if the circulation is free. Even with the circulation arrested, the hand takes a long time to come into equilibrium with cold water in a calorimeter. For example, by the 6th min. (Table 1) the total heat output from 100 ml. of hand was 1126 cal., and by the 10th min cal. Assuming a specific heat of 0-71 and a specific gravity of 1-13 (Stewart, 1911), one would expect 385 ml. of hand at 29 C., when inserted into 4000 g. of water

4 462 A. D. M. GREENFIELD, J. T. SHEPHERD AND R. F. WHELAN at C., to come into equilibrium at a final temperature of C., the hand releasing 2031 cal./100 ml. in so doing. It follows that at the 6th min. the hand had given up only 55-4 % and at the 10th min. only 64-4% of the TABLE 1. Calorimetric observations on the left hand of R. F. W., with the circulation arrested. At - 1 min. the hand was removed from a water-bath at 29GC. with which it had been equilibrated for 20 min. and dried. At min. a cuff was inflated on the left arm to 250 mm. Hg. At 0 min. the hand was inserted in the calorimeter. Hand vol. 385 ml. Water equivalent of calorimeter and contents (other than immersed hand) 4000 g. Temperature rise Heat output from Calorimeter due to immersed immersed hand temperature Temperature rise hand (cal./100 ml. Time in min. (O C.) (milli C./min.) (milli C./min.) hand/min.) Observations discontinued at the 11th minute because of very severe pain. TABLE 2. Calorimetric observations on the left hand of R. F. W., with the circulation free. At - 1 min. the left hand was removed from a water-bath at 290 C. with which it had been equilibrated for 30 min. and dried. At 0 min. it was inserted in the calorimeter. Hand vol. 450 ml. Water equivalent of calorimeter and contents (other than immersed hand) 4000 g. Time in min Calorimeter temperature (O C.) Heat output Heat output Temperature from immersed due to blood Temperature rise due to hand (cal./ flow (cal./ rise immersed hand 100 ml. hand/ 100 ml. hand/ (milli C./min.) (mill C./min.) min.) min.) ( -58) 12 ( -5) expected total. The average internal temperature of the hand at the 6th and at the 10th min. were, by calculation, 14-9 and C. respectively. Thus the hand equilibrates much more slowly than the finger tip, which was found by

5 HEAT LOSS FROM THE HAND 463 Greenfield, Shepherd & Whelan (1950) to come within 2% of equilibrium by the 7th min. It follows from this that the heating of the hand by warm blood commences at a time when the hand is still considerably above the calorimeter temperature. The amount of heat derived from the cooling of the hand with the circulation free (omitting any heat from circulating blood) is therefore less than that derived from the cooling of the hand with the circulation arrested; in the former case the hand does not cool to so low a temperature as in the latter R.F.W ~~ ~~~~~~0 0 U Soo o co 10 ~ Minutes Minutes Fig. 2. The heat loss from the left hand of R. F. W. into a calorimeter in the 0-6' C. range (left rectangle) and from the right hand into a calorimeter in the 29-32O C. range (right rectangle). The left hand was transferred from water at 290 C. to the calorimeter at 0 min. On the left side, the upper line represents the total heat loss, and the black area the deduced heat loss from the circulating blood. Heat loss is expressed in cal./100 ml./min. The calorie scales differ on the two sides, but have been chosen so that the scales of minimum blood flow correspond. The minimum blood flows have been calculated as described in the text and are expressed in ml./100 ml./min. Pain is shown on a roughly quantitative scale at the top of the figure. The deduction we have made (Table 2, columns 5 and 6) for the heat due to the cooling of the hand is therefore too large, and it follows that on this count we underestimate the amount of heat derived from the circulating blood. (5) We do not know the amount of metabolic heat formed under the condition of our experiments. If we accept Stewart's (1911) figure of 5 cal./min. for the whole hand, it is clear that the metabolic heat is very small compared with the heat losses observed in our experiments. It is unlikely that the errors mentioned seriously upset our estimate of the heat derived from the circulating blood. They in no way affect our figures for the total heat loss from the hands.

6 O-60 C C. A.D.M.G. 060 C C. R. F.W. IN,i i J.T.S. M.F.R. Fig. 3. The heat loss from the hand of four normal subjects into water in the 0 60 C. range. The experiment on R. F. W. is the same as that shown with the scales fully marked in Fig. 2. The conventions in the other figures are the same. That is, on the 0 60 C. side the marks are at 500 and 1000 cal./100 ml. hand/min. and on the C. side at 100 and 200 cal./100 ml. hand/min. In every case the full width of each rectangle represents 45 min. 0-6'C C. Fig. 4. The heat loss from the distal 2-8 cm. of the index fingers of M. F. R. into water in the 0)60 C. range (left figure) and into water in the C. range (right figure). The heat loss has been expressed in the same way as in Fig. 3 and the scales are identical.

7 HEAT LOSS FROM THE HAND 465 Heat loss from hands with the circulation free. In all experiments one hand was observed in a calorimeter at C. (Cooper, Cross, Greenfield, Hamilton & Scarborough, 1949) before and during observations of the other hand in 0-60 C C C. 0-6 C. R. F.W. 1~A'YL k~uul I. I A.R. Fig. 5. The heat loss from the four fingers of six normal subjects into water in the 06 C. range. The conventions are as in Figs. 2 and 3. A. D. M. G., R. F. W., J. T. S., left fingers cold; M. F. R., J. H. C., A. R., right fingers cold. a calorimeter at 0-6 C. The observations on the cold side in the initial period of a typical experiment are shown in Table 2. It can be seen that in the first 4 min. of immersion in the cold water, the amount of heat given off per 100 ml. of immersed hand was little different whether the circulation was free or arrested.

8 466 A. D. M. GREENFIELD, J. T. SHEPHERD AND R. F. WHELAN In the 1st and 3rd min. more heat was given off with the circulation arrested; it is difficult to explain these discrepancies, which were greater in this experiment than in most of the others. Clearly the blood flow must have been negligible during this period. After the 5th min. an increasingly large amount of heat was lost when the circulation was free, reaching a peak at 10 min. and then slowly declining. The experiment was terminated at the 28th min. because the calorimeter temperature had risen above 60 C., the limit of the thermometer scale. The results of this experiment are shown in Fig. 2. We do not know the temperature of the arterial blood arriving at the hand or of the venous blood leaving it. It is impossible therefore to calculate accurately the hand blood flow from the heat exchange. If we assume that the blood arrives at 370 C. and leaves at 00 C., we can arrive at a figure which we call the 'minimum blood flow' and which we are certain is less than the real blood flow (Greenfield & Shepherd, 1950). The second scale in Fig. 2 shows the minimum blood flow calculated on this basis. The results of this and three similar experiments are shown in Fig. 3. After immersing the hand in cold water the heat elimination from the circulating blood was small or negligible for about 5 min. and then rapidly increased. It reached a maximum by the 7th-lOth min. and then either declined slowly or remained fairly steady. All these experiments had to be ended when the temperature of the water in the calorimeter had reached 60 C. Pain started almost immediately after immersing the hand and was very severe until the heat elimination began to rise. Occasionally pain was absent during the remainder of the experiment, but more often a dull ache persisted or came on towards the end. The changes in heat loss on the control side in a calorimeter at C. often reflected the changes on the cold side. The initial insertion of the hand into the cold water caused a transient decrease in the heat loss from the opposite hand, which we interpreted as being due to reflex vasoconstriction. The heat loss from unit volume of hand is much less than from unit volume of finger tip. Fig. 4 shows the heat loss from the finger tip of M.F.R. measured by the method of Greenfield & Shepherd (1950). This result is typical for a finger tip immersed in water at 0-6 C., and when compared with the result obtained for the whole hand of this subject (Fig. 3) shows that the maximum heat loss from the finger tip in cal./100 ml./min. was over 10 times greater than the maximum from the hand. The heat eliminationfrom thefingers to water at 0-6 C. The standard procedure was similar to that employed in the case of the hand. The hands were immersed in a water-bath at 290 C. for at least 20 min., dried, and the fingers inserted into a calorimeter containing water at about 10 C.

9 HEAT LOSS FROM THE HAND 467 The other hand was similarly treated, but the fingers were inserted about 5 min. earlier into another calorimeter containing water at about 290 C. TABLE 3. Calorimetric observations on the left fingers of A. D. M. G. with the circulation arrested. At - 2 min. a cuff was inflated on the left arm to 220 mm. Hg. At -1 min. the hand was removed from a water-bath at 290 C. with which it had been equilibrated for 20 min. and dried. At 0 min. the fingers were inserted into the calorimeter. Finger vol. 64 ml. Water equivalent of the calorimeter and contents (other than immersed fingers) 4170 g. Temperature Heat output from Calorimeter rise due to immersed fingers temperature Temperature rise immersedfingers (cal./100 ml. Time in min. (O C.) (milli C./min.) (milli C./min.) finger/min.) Observations discontinued at the 8th minute because of severe pain. TABLE 4. Calorimetric observations on the left fingers of A. D. M. G. with the circulation free. At - 1 min. the left hand was removed from a water-bath at 29 C. with which it had been equilibrated for 20 min. and dried. At 0 min. it was inserted in the calorimeter. Finger vol. 64 ml. Water equivalent of calorimeter and contents (other than immersed hand) 4170 g. Temperature Heat output Heat output rise due to from immersed due to blood Calorimeter Temperature immersed fingers (cal./ flow (cal. temperature rise fingers 100 ml. 100 ml. Time in min. (O C.) (milli0 C./min.) (milli C./min. finger/min.) finger/min.) Heat loss from the fingers with the circulation arrested. It is nearly as painful to immerse the fingers in water at about 10 C. as it is to immerse the whole hand. Observations were made on one occasion only, and the results are shown PH. CXII. 30

10 468 A. D. M. GREENFIELD, J. T. SHEPHERD AND R. F. WHELAN in Table 3. The temperature rise due to the immersed fingers was 152 milli' C. in the 1stmi., but only 7 milli' C. in the 8th min., by which time it is estimated that the heat lost was 96% of the expected total quantity lost in attaining equilibrium. These figures have been used to calculate, in this and other subjects, the heat loss from the circulating blood. After the 8th min. it was assumed that all the heat lost from the fingers came from the circulating blood. The errors involved in the calculation are similar to those already discussed in the case of the hand. They are, however, relatively much smaller. They in no way affect our figures for the total heat loss from the fingers. Heat loss from the fingers with the circulation free. The fingers of one hand were observed in a calorimeter at C. before and during observations on the other hand in a calorimeter at 0-6 C. The observations on the cold side in the initial period of a typical experiment are shown in Table 4. Experiments of this kind were carried out on six subjects and the results are shown in Fig. 5. Observations were usually continued until the temperature of the calorimeter had reached the limit of the thermometer scale, but in one case (A. R.) they were stopped because of a vasovagal attack after immersion in the cold water for 17 min. The heat loss from circulating blood was negligible for the first 5 min. A very rapid increase in the rate of heat loss followed in all cases, and reached a peak at about the 10th min. The subsequent pattern varied from subject to subject. Usually there was a slow decrease in heat loss interspersed with temporary increases. As in the hand, pain was severe when the rate of heat loss was low, and absent or slight when it was high. The initial insertion of the fingers into the cold water caused a transient decrease in the heat loss from the fingers of the opposite hand. Heat loss from thefingers under different environmental conditions The heat loss from the fingers of one of these subjects (J. T. S.) was determined on three separate occasions under three different environmental conditions. These were: (a) Almost naked in a cold room with two electric fans directed towards the body and with both feet and calves in iced water. The whole length of each arm down to the fingers was protected with heavy wool scarves in order to prevent extra pre-cooling of the arterial blood. (b) Normally clothed in a room at 210 C. (c) Wrapped in blankets in a room at 230 C. with the feet and calves in a stirred water-bath at 440 C. The results of these three experiments are shown in Fig. 6. With the subject generally cold (upper rectangles, Fig. 6), while there was practically no heat loss from the fingers in a calorimeter at C., indicating a state of peripheral vasoconstriction, a slight transient vasodilatation still occurred in the opposite fingers immersed in a calorimeter at 0-6' C. This was only sufficient, however, to cause a temporary reduction in the severe pain, and the experiment had to

11 0-60C. HEAT LOSS FROM THE HAND C C 0-6 C. 469 J.T.S. A.D.M.G. I Fig C. 0-60C. Fig. 6. Fig. 8. Fig. 6. The heat loss from the four fingers of J. T. S. into water in the 0-6 C. range under three different environmental conditions. Top figure: almost naked in a cold room with two electric fans directed towards the body and with both feet and calves in iced water. The whole length of each arm down to the fingers was wrapped in heavy wool scarves. Middle figure: normally clothed in a room at 210 C. Lower figure: wrapped in blankets in a room at 230 C. with the feet and calves in a stirred water-bath at 440 C. The conventions are as in Figs. 2 and 3, but the height of the lower figure has been increased without changing the scales. Fig. 7. Simultaneous observations of the heat Joss from the four fingers of the right and left hands into water in the 06 C. range. The conventions are as in Figs. 2 and 3. Fig. 8. Simultaneous observations of the heat loss from the hands of A. D. M. G. into water in the 0 60 C. range. The conventions are as in Figs. 2 and

12 470 A. D. M. GREENFIELD, J. T. SHEPHERD AND R. F. WHELAN be terminated after the 19th min. The maximum heat loss was 350 cal./100 ml. finger/mmn. With the subject comfortably warm (middle rectangles, Fig. 6) the heat loss following the initial decrease reached 460 cal./100 ml. finger/min., and varied between 300 and 480 throughout the remainder of the experiment. Under these conditions the fingers were painful for the first eleven minutes only. When the subject was very warm (lower rectangles, Fig. 6) the heat loss from the circulating blood was high in the first 5 min. It then fell, but never to zero, and at the 9th min. began to increase rapidly, reaching a value of 1580 cal./100 ml. finger/min. by the 16th min. The limit of the thermometer scale was reached at the 25th min. The pain was only severe in the 7th and 8th mins. and disappeared completely at the 10th min. From the 12th min. onwards the fingers on the cold side felt warmer than the opposite fingers which were in water at C. Simultaneous observations of the heat loss on the two sides In two subjects the heat losses from the fingers of the right and left hands were compared simultaneously at 0-6o C. (Fig. 7). While there were slight dcwerences, the general behaviour was symmetrical. The response of the two hands of these subjects was also compared in the same temperature range (Figs. 8, 9) with similar results. In all these experiments, when the cold vasodilatation started, the pain in the fingers or hand became less severe or disappeared. At the same time a sensation of cold, and often of pain, was felt just above the water level, and mainly on the dorsum of the hand or wrist. This gradually spread up the arm; the pain usually subsided in a few minutes, but the sensation of cold usually persisted. The rate of heat loss showed that the circulation was completely or almost completely arrested for the first 5 min. Little or no cold blood would therefore return in the veins during this time. When the vasodilatation started, very cold blood would flow up the veins in large quantities. It seemed likely that this was th-e explanation of the sensations. To test this hypothesis the temperature of the skin over a prominent dorsal vein, about 5 cm. above the water level, was measured with a thermoelectric junction held in place by one layer of adhesive plaster; one junction was on the side with the fingers or hand in water at 0-6O C. and another on the control side at C. In seven experiments on six subjects the temperature on the control side remained at a more or less constant level about 290 C. throughout the experiment. On the side with the fingers or hand in the calorimeter at 0-6 C., the temperature remained nearly constant at about 290 C. during the initial period, when the measurements of heat loss showed that blood flow was very small. It then dropped sharply to C. over the next 5-11 min. as the cold vasodilatation started and the calorie output increased. This drop in temperature was ac-

13 HEAT LOSS FROM THE HAND 471 companied by a sensation of cold and often of pain in the dorsum of the hand. During the remainder of the experiment the temperature fell a further 2-3' C. In one of the two experiments in which both hands were immersed in calorimeters at 0-6' C. recordings were made of the oesophageal temperature as well Time in minutes Fig. 9. Simultaneous observations of the heat loss in cal./100 mj./min. from the two hands of R. F. W. into water at 046 C. The temperature of a thermoelectric junction applied to the skin over a vein on the dorsum of each wrist is shown below the graph of heat loss from the corresponding hand. The temperature of a thermoelectric junction in the oesophagus 40 cm. from the incisor teeth is shown at the bottom. as of the skin temperature over a large wrist vein on each side. The former was measured by a thermoelectric junction in the end of a Ryle's tube 40 cm. from the incisor teeth. Readings were accurate to C., and the system was calibrated before and after the experiment. The results are shown in Fig. 9. During the initial period, when the pain was at its maximum and the heat loss

14 472 A. D. M. GREENFIELD, J. T. SHEPHERD AND R. F. WHELAN from circulating blood negligible, the skin and oesophageal temperatures remained unchanged. At the 5th min., when the heat loss indicated vasodilatation, the pain left the hands and moved into the wrists and arms which now felt cold. At the same time the temperature of the skin over the wrist veins began to drop, falling 100 C. in 4 min. At the 7th min. the oesophageal temperature began to fall from C., reaching C. 8 min. later. This shows that a large volume of cold blood was returning to the body. The oesophageal temperature rose from the 15th min. until the end of the experiment, when it was C. There was no shivering, but the subject felt an involuntary increase in muscle tension which may have contributed to this small rise in temperature. A comparison of the heat elimination from the finger tip, fingers and hand at the height of cold vasodilatation Fig. 10 shows the heat losses in calories per minute from the whole hand, the four fingers of one hand and one finger tip when immersed in a calorimeter at 0-6 C. All figures refer to heat loss at the height of cold vasodilatation. The values for the finger tip are taken from a previous paper (Greenfield & Shepherd, 1950). Little more heat is lost from the whole hand than from the four fingers, but the whole hand loses about eight times as much heat as does a single finger tip. In Fig. 11 the same results are shown, but the heat loss has been expressed in cal./100 ml. tissue/min. It is clear that the finger tip loses more heat per unit of volume than do the four fingers. The four fingers in turn lose more heat than does the whole hand. In one subject (J. T. S.) the surface areas of the immersed parts have been measured by the two methods already described. These showed respectively that the distal 2 8 cm. of index finger was 2-85 or 2 7 % of the total area of the hand, and that the area of the immersed parts of the four fingers was 30 or 27-7 % of the total area of the hand. The averaged results by the two methods were, for the finger tip 14-5 sq.cm., for the four fingers 151 sq.cm., and for the whole hand 523 sq.cm. The heat losses to water at 0-60 C. at the height of cold vasodilatation in this subject were for the finger tip 6-9, for the four fingers 2-45, and for the whole hand 141 cal./sq.cm./min. The finger tip, therefore, loses more heat per unit of area, as well as per unit of volume, than do the four fingers; these in turn lose more heat than does the whole hand. DISCUSSION The heat loss from the terminal 2-8 cm. of the index finger immersed in water at 0-6' C. varies at the height of cold vasodilatation from 1100 to 3400 cal./ 100 ml./min. (Greenfield & Shepherd, 1950). If, when the whole hand is immersed, the heat loss were proportional to that of the finger tip, it would amount on the average to 530, and in some persons to as much as 840 kg.cal./hr.

15 HEAT LOSS FROM THE HAND 473 In fact, however, at the height of cold vasodilatation we find that the average heat loss from the four fingers is only 36, and from the whole hand only 90 c 4) L- o u 1V 60 ' -) v 4A 30.~ 0 v e 30 A.D.M.G. J.T.S. R.F.W. M.F.R. J.H.C. A.R. Fig. 10. The heat losses from (a) the whole hand (black columns), (b) the four fingers (oblique hatching) and (c) the distal 2*8 cm. of the index finger (clear columns) of six normal subjects. Heat loss is expressed in small cal./min. (not small cal./100 ml. tissue/min.) and in kg.cal./hr. A.D.M.G. J.T.S. R.F.W. M.F.R. J.H.C. A.R. Fig. 11. The heat losses from (a) the whole hand (black columns), (b) the four fingers (oblique hatching) and (c) the distal 2-8 cm. of index finger (clear columns) of six normal subjects. Heat loss is expressed in small cal./100 ml. of tissue/min. 48 kg.cal./hr. There are two main reasons for these differences. First, the circulation through the fingers is capable of passing a great deal more blood

16 474 A. D. M. GREENFIELD, J. T. SHEPHERD AND R. F. WHELAN per unit volume per minute than that through the whole hand (Wilkins, Doupe & Newman, 1938). Secondly, more heat may be lost from unit volume of blood passing through the finger than through the hand. The absolute quantity of heat lost from a single finger tip is only about one-eighth of that lost from the whole hand (Fig. 10). The returning venous blood from a single finger tip may therefore be expected to cause less cooling of the arm and hence less pre-cooling of the arterial blood. There is no doubt that the fingers and the whole hand are capable of cold vasodilatation. The extent of the response is modified by the level of peripheral vasodilatation or constriction as judged by the heat loss from the control side. It still occurs, however, in spite of marked general vasoconstriction due to cooling of the body as a whole (Fig. 6). Without an accurate knowledge of the temperature of the blood entering and leaving the hand when immersed in water at 0-6 C. we cannot translate figures for heat loss into actual blood flow. The minimum figures we have calculated (Fig. 2) on the basis of blood arriving at 370 C. and leaving at 00 C. are almost certainly much too small. Bazett, Love, Newton, Eisenberg, Day & Forster (1948) have recorded temperatures as low as C. in the radial artery of a subject in a room at 90 C. This suggests that in our experiments the temperature in the radial artery on the cold side may have been well below 370 C. The temperature of the skin over the dorsal veins (Fig. 9) suggests that the temperature of the blood leaving the hand was considerably above 00 C. Measurements of heat loss when the hands or the fingers are immersed in water at 0-60 C. suggest that there is initially almost complete arrest of the circulation, followed, after 5-7 min., by a large flow of blood. This deduction is supported by observation of the oesophageal temperature and of the skin temperature over the dosal veins proximal to the immersed area. Because of the thermal lag of the system, the actual rate of change in blood flow is probably much greater than would appear from the figures. The thermal lag is mainly in the immersed tissues. The calorimeter and thermometer settle within one minute at a new temperature after a suddenly imposed temperature change. The release of heat from the hand (Table 1) or from the fingers (Table 3) is much slower. The pain on immersing the whole hand in cold water was worse but not very much worse than when one finger tip was immersed. It still bore the same relationship to the heat loss from circulating blood as it did in the case of the tip of the index finger (Greenfield & Shepherd, 1950). That is, pain was felt when the loss was low and not when it was high. SUMMARY 1. A method is described for measuring the heat loss from the fingers or from the whole hand into water between 0 and 60 C.

17 HEAT LOSS FROM THE HAND A comparison of the heat loss with the circulation free and arrested enables the heat loss from the circulating blood to be calculated. The uncertainties in the calculation are discussed. 3. There is very little heat loss from circulating blood during the first 5 min. of immersion; the heat loss then rapidly rises to a high value, averaging at the height of cold vasodilatation, 200 cal./100 ml./min. in the hand and 877 cal./ 100 ml./min. in the fingers. The corresponding figure for the distal 2-8 cm. of the index finger has previously been found to be 2200 cal./100 ml./min. 4. The average heat loss from one hand at the height of cold vasodilatation is at the rate of 48 kg.cal./hr., and from the fingers of one hand, 36 kg.cal./hr. Previous observations have shown that the average loss from the distal 2-8 cm. of the index finger is 6 kg.cal./hr. 5. In one subject, heat loss per sq.cm. was calculated at the height of cold vasodilatation from the tip of one finger (6.9 cal./min.), the four fingers (2.45 cal./min.) and the whole hand (1.1 cal./min.). 6. The heat loss is reduced when the subject is generally cold, and increased when he is hot. 7. The heat loss from the hands or fingers of a subject is symmetrical. 8. The returning venous blood during cold vasodilatation may reduce the temperature of the skin overlying veins proximal to the immersed part by as much as 100 C. in 4 min. When both hands are immersed, the oesophageal temperature may fall C. in 8 min. 9. The relationship of pain to these events is described. 10. The results show that, at the height of cold vasodilatation, the blood flow must be not less than 5.5 ml./100 ml. hand/min. and not less than 24 ml./100 ml. fingers/min. The flows are probably much greater than this, but the available information does not permit a quantitative comparison with the maximum blood flow obtainable by other methods of vasodilatation. We wish to thank the students who acted as subjects for some of the experiments. The thermometers were supplied by Messrs B. Black and Son Ltd., 180 Goswell Road, London, E.C. 1. REFERENCES Barcroft, H. & Edhoim, 0. G. (1943). J. Physiol. 102, 5. Bazett, H. C., Love, L., Newton, M., Eisenberg, L., Day, R. & Forster, R. (1948). J. appl. Phy8iol. 1, 3. Cooper, K. E., Cross, K. W., Greenfield, A. D. M., Hamilton, D. McK. & Scarborough, H. (1949). Clin. Sci. 8, 217. Greenfield, A. D. M. & Scarborough, H. (1949). Clin. Sci. 8, 211. Greenfield, A. D. M. & Shepherd, J. T. (1950). Clin. Sci. 9, 323. Greenfield, A. D. M., Shepherd, J. T. & Whelan, R. F. (1950). Clin. Sci. 9, 349. Lewis, T. (1930). Heart, 15, 177. McCorry, R. L. (1950). Personal communication. Stewart, G. N. (1911). Heart, 3, 33. Wilkins, R. W., Doupe, J. & Newman, H. W. (1938). Clin. Sci. 3, 403.

(E.M.I.), age years. In the main series of experiments, twenty-four in all,

(E.M.I.), age years. In the main series of experiments, twenty-four in all, 63 J. Physiol. (I95I) II3, 63-72 THE PROPORTION OF THE TOTAL HAND BLOOD FLOW PASSING THROUGH THE DIGITS A. D. M. GREENFIELD, J. T. SHEPHERD AND R. F. WHELAN From the Department of Physiology, The Queen's

More information

plethysmographic methods that when the subject was pinched on the upper

plethysmographic methods that when the subject was pinched on the upper 24 J. Physiol. (I95I) II2, 24-2I 6I2.I5.6II.976 THE DECREASE IN HAND BLOOD FLOW FOLLOWING INFLATION OF AN ARTERIAL OCCLUSION CUFF ON THE OPPOSITE ARM BY IAN C. RODDIE From the Department of Physiology,

More information

(fig. 3) must be at the same temperature as the water in this chamber CALORIMETRIC STUDIES OF THE EXTREMITIES

(fig. 3) must be at the same temperature as the water in this chamber CALORIMETRIC STUDIES OF THE EXTREMITIES CALORIMETRIC STUDIES OF THE EXTREMITIES II. EXPERIMENTAL APPARATUS AND PROCEDURES' By ROY KEGERREIS (Received for publication July 1, 1926) The calorimeter used in these experiments is a modification of

More information

(Received 27 July 1955)

(Received 27 July 1955) 277 J. Physiol. (I956) I3I, 277-289 THE REACTIONS OF THE BLOOD VESSELS OF THE HAND DURING INCREASES IN TRANSMURAL PRESSURE BY D. R. COLES AND A. D. M. GREENFIELD From the Department of Physiology, The

More information

transients' of large amplitude can be imposed on the arterial, cardiac and Since both coughing and the Valsalva manoeuvre raise intrathoracic pressure

transients' of large amplitude can be imposed on the arterial, cardiac and Since both coughing and the Valsalva manoeuvre raise intrathoracic pressure 351 J. Physiol. (I953) I22, 35I-357 EFFECTS OF COUGHING ON INTRATHORACIC PRESSURE, ARTERIAL PRESSURE AND PERIPHERAL BLOOD FLOW BY E. P. SHARPEY-SCHAFER From the Department of Medicine, St Thomas's Hospital

More information

Medical Center, San Francisco, Cal.,

Medical Center, San Francisco, Cal., 628 J. Phy8iol. (1966), 183, 628-636 With 4 text-figure8 Printed in Great Britain THE INTERRELATION OF THERMOREGULATORY AND BARORECEPTOR REFLEXES IN THE CONTROL OF THE BLOOD VESSELS IN THE HUMAN FOREARM

More information

APPENDIX. working blood volume was also rather large; Evans, Grande, and. equilibrated to the new mixture is partially dependent upon the rate

APPENDIX. working blood volume was also rather large; Evans, Grande, and. equilibrated to the new mixture is partially dependent upon the rate 612.172-5 APPENDIX A SIMPLIFIED HEART OXYGENATOR CIRCUIT FOR BLOOD- FED HEARTS. By J. YULE BOG-UE and R. A. GREGORY.' SINCE 1934 studies on the carbohydrate metabolism of the blood-fed heart without lungs

More information

(Received 25 November 1957)

(Received 25 November 1957) 281 J. Physiol. (958) 14, 28-29 THE EFFECTS OF HEXAMETHONUM BROMDE ON TEMPERATURE REGULATON N MAN BY A. C. L. HSEH From the Department of Physiology, University of Hong Kong (Received 25 November 1957)

More information

Experiment 13: Make-Up Lab for 1408/1420

Experiment 13: Make-Up Lab for 1408/1420 Experiment 13: Make-Up Lab for 1408/1420 This is only for those that have approval. Students without approval will not be allowed to perform the lab. The pre-lab must be turned in at the beginning of lab.

More information

A SIMPLE TITRATION METHOD FOR DETERMINING THE SPECIFIC GRAVITY ON ONE DROP OF URINE

A SIMPLE TITRATION METHOD FOR DETERMINING THE SPECIFIC GRAVITY ON ONE DROP OF URINE J. clin. Path. (1951), 4, 491. A SIMPLE TITRATION METHOD FOR DETERMINING THE SPECIFIC GRAVITY ON ONE DROP OF URINE BY From the Pathological Laboratory, the Peace Memorial Hospital, Watford (RECEIVED FOR

More information

(Bayliss, 1902; Folkow, 1949). The reaction, according to its strength and the

(Bayliss, 1902; Folkow, 1949). The reaction, according to its strength and the 614 J. Physiol. (1959), 149, pp. 614-62-5) With 4 text-figure8 Printed in Great Britain THE INCREASE IN TONE IN FOREARM RESISTANCE BLOOD VESSELS EXPOSED TO INCREASED TRANSMURAL PRESSURE BY D. A. BLAIR,

More information

BASIC LABORATORY TECHNIQUES (Revised )

BASIC LABORATORY TECHNIQUES (Revised ) BASIC LABORATORY TECHNIQUES (Revised 1-2-16) (See Appendix II: Summary for making Spreadsheets and Graphs with Excel and Appendix III parts C, C1 and C2: Significant figures, scientific notation and rounding)

More information

Gas Laws. Introduction

Gas Laws. Introduction Gas Laws Introduction In 1662 Robert Boyle found that, at constant temperature, the pressure of a gas and its volume are inversely proportional such that P x V = constant. This relationship is known as

More information

BASIC LABORATORY TECHNIQUES (Revised )

BASIC LABORATORY TECHNIQUES (Revised ) BASIC LABORATORY TECHNIQUES (Revised 1-6-13) A. WEIGHING The determination of the quantity of matter in a sample is most directly determined by measuring its mass. The process by which we determine the

More information

(Received 9 September 1940)

(Received 9 September 1940) 257 J. Physiol. (I 94I) 99, 257-264 6I2.2II A METHOD OF RECORDING THE RESPIRATION BY J. H. GADDUM From the College of the Pharmaceutical Society, 17 Bloomsbury Square, London, W.C. 2 (Received 9 September

More information

Lung Volumes and Capacities

Lung Volumes and Capacities Lung Volumes and Capacities Normally the volume of air entering the lungs during a single inspiration is approximately equal to the volume leaving on the subsequent expiration and is called the tidal volume.

More information

IN experimental plant physiology the problem of the control of

IN experimental plant physiology the problem of the control of [ 119 ] THE CONTROL OF ATMOSPHERIC HUMIDITY IN A CLOSED SYSTEM BY B. D. BOLAS From the Department of Plant Physiology and Pathology, Imperial College of Science and Technology, London (With 4 figures in

More information

Module No GETTING ACQUAINTED GENERAL GUIDE TIMEKEEPING

Module No GETTING ACQUAINTED GENERAL GUIDE TIMEKEEPING Module No. 2196 2196-1 GETTING ACQUAINTED Congratulations upon your selection of this CASIO Pressure Monitor Watch (BP-1B, Module No. 2196). To get the most out of your purchase, be sure to carefully read

More information

USE OF TIRE PRESSURE TO IMPROVE THE CALIBRATION OF THE BICYCLE W...

USE OF TIRE PRESSURE TO IMPROVE THE CALIBRATION OF THE BICYCLE W... Page 1 of 8 PROPOSED USE OF TIRE PRESSURE TO IMPROVE THE CALIBRATION OF THE BICYCLE WHEEL IN THE MEASUREMENT OF ROAD-RACING COURSES ABSTRACT NEVILLE F WOOD nfwood@hotmail.com Revised 6/3/05 I have shown

More information

CONTENTS SPECIFICATIONS GENERAL INFORMATION RECOMMENDED USE OPERATING PRINCIPLE TIPS ON TAKING YOUR BLOOD PRESSURE 3-4 BATTERY INSTALLATION

CONTENTS SPECIFICATIONS GENERAL INFORMATION RECOMMENDED USE OPERATING PRINCIPLE TIPS ON TAKING YOUR BLOOD PRESSURE 3-4 BATTERY INSTALLATION IFU SBPMON107 CONTENTS SPECIFICATIONS GENERAL INFORMATION RECOMMENDED USE OPERATING PRINCIPLE TIPS ON TAKING YOUR BLOOD PRESSURE BATTERY INSTALLATION CORRECT POSITION FOR MEASUREMENT POSITIONING THE CUFF

More information

THERMALLING TECHNIQUES. Preface

THERMALLING TECHNIQUES. Preface DRAFT THERMALLING TECHNIQUES Preface The following thermalling techniques document is provided to assist Instructors, Coaches and Students as a training aid in the development of good soaring skills. Instructors

More information

Lab #2: Blood pressure and peripheral circulation

Lab #2: Blood pressure and peripheral circulation Lab #2: Blood pressure and peripheral circulation Vertebrates have a closed circulatory system where the blood is always enclosed within blood vessels or the heart. Blood is pumped from the heart (the

More information

J. Physiol. (I941) I00, I98-21I 6I :6I2.825

J. Physiol. (I941) I00, I98-21I 6I :6I2.825 198 J. Physiol. (I941) I00, I9821I 6I2.22.02:6I2.825 THE EFFECT OF OXYGEN LACK ON THE CEREBRAL CIRCULATION BY F. C. COURTICE From the Departments of Physiology and of Surgery, Oxford (Received 24 March

More information

Characterizers for control loops

Characterizers for control loops Characterizers for control loops By: F. G. Shinskey (May 1999) Introduction Commercial controllers such as the PID series (proportional, integral, derivative, and their combinations) are linear devices

More information

Additional Reading General, Organic and Biological Chemistry, by Timberlake, chapter 8.

Additional Reading General, Organic and Biological Chemistry, by Timberlake, chapter 8. Gas Laws EXPERIMENTAL TASK Determine the mathematical relationship between the volume of a gas sample and its absolute temperature, using experimental data; and to determine the mathematical relationship

More information

CARBOXYHAEMOGLOBIN IN A FINGER PRICK SAMPLE

CARBOXYHAEMOGLOBIN IN A FINGER PRICK SAMPLE Brit. J. industr. Med., 1965, 22, 139. A SENSITIVE METHOD FOR THE DETERMINATION OF CARBOXYHAEMOGLOBIN IN A FINGER PRICK SAMPLE OF BLOOD BY B. T. COMMINS and P. J. LAWTHER From the Medical Research Council,

More information

ConcepTest PowerPoints

ConcepTest PowerPoints ConcepTest PowerPoints Chapter 10 Physics: Principles with Applications, 6 th edition Giancoli 2005 Pearson Prentice Hall This work is protected by United States copyright laws and is provided solely for

More information

Lab 5- Cellular Respiration

Lab 5- Cellular Respiration Lab 5- Cellular Respiration Background: Many cellular processes require energy. Aerobic cellular respiration supplies energy by the oxidation of glucose. This is a complex process involving a number of

More information

that, as a means of progression, walking is suitable for lower speeds

that, as a means of progression, walking is suitable for lower speeds 2 6I2 744.22 ENERGY EXPENDITURE IN WALKING AND RUNNING. BY M. OGASAWARA. (From the Department of Industrial Physiology, London School of Hygiene and Tropical Medicine.) (Received February 28, 1934.) IT

More information

General Accreditation Guidance. User checks and maintenance of laboratory balances

General Accreditation Guidance. User checks and maintenance of laboratory balances General Accreditation Guidance User checks and maintenance of laboratory balances January 2018 Copyright National Association of Testing Authorities, Australia 2010 All intellectual property rights in

More information

PROBLEM SET 7. Assigned: April 1, 2004 Due: April 9, 2004

PROBLEM SET 7. Assigned: April 1, 2004 Due: April 9, 2004 Harvard-MIT Division of Health Sciences and Technology HST.542J: Quantitative Physiology: Organ Transport Systems Instructors: Roger Mark and Jose Venegas MASSACHUSETTS INSTITUTE OF TECHNOLOGY Departments

More information

A Hare-Lynx Simulation Model

A Hare-Lynx Simulation Model 1 A Hare- Simulation Model What happens to the numbers of hares and lynx when the core of the system is like this? Hares O Balance? S H_Births Hares H_Fertility Area KillsPerHead Fertility Births Figure

More information

OXYGEN POWER By Jack Daniels, Jimmy Gilbert, 1979

OXYGEN POWER By Jack Daniels, Jimmy Gilbert, 1979 1 de 6 OXYGEN POWER By Jack Daniels, Jimmy Gilbert, 1979 Appendix A Running is primarily a conditioning sport. It is not a skill sport as is basketball or handball or, to a certain extent, swimming where

More information

THE EFFECT OF LOCAL COOLING ON THE FILTRATION AND ABSORPTION OF FLUID IN THE HUMAN FOREARM

THE EFFECT OF LOCAL COOLING ON THE FILTRATION AND ABSORPTION OF FLUID IN THE HUMAN FOREARM THE EFFECT OF LOCAL COOLING ON THE FILTRATION AND ABSORPTION OF FLUID IN THE HUMAN FOREARM By ELLEN BROWN,' CHARLES S. WISE,2 AND EDWIN 0. WHEELER 8 (From the Department of Physiology, Harvard Medical

More information

EXERCISE 8: BLEEDING TIME

EXERCISE 8: BLEEDING TIME EXERCISE 8: BLEEDING TIME Skills: 20 points Objectives: 1. Properly prepare patient prior to performance of the bleeding time procedure. 2. Ascertain prior to performance of the procedure whether or not

More information

Cell Respiration Laboratory PSI Biology

Cell Respiration Laboratory PSI Biology Cell Respiration Laboratory PSI Biology Name Objective Students will understand the relationship between temperature, pressure, and gas volume and will predict the effect of temperature and germination

More information

II. MATERIALS REQUIRED FOR PERFORMANCE TESTING

II. MATERIALS REQUIRED FOR PERFORMANCE TESTING TSP-016 P/N L038-058 4-001 Rev. D February 8, 2000 Page 1 of 14 DISTRIBUTION: VistaLab Technologies Customers EQUIPMENT: MLA Pipettes SUBJECT: Pipette Performance Verification Protocol PURPOSE: To evaluate

More information

Working Efficiency, Department of Human Anatomy, University of Oxford

Working Efficiency, Department of Human Anatomy, University of Oxford 1 J. Physiol. (I953) I2I, I-27 THE MEASUREMENT OF VOLUME CHANGES IN HUMAN LIMBS BY R. J. WHITNEY From the Medical Research Council Unit for Research on Climate and Working Efficiency, Department of Human

More information

counterweighting there is freedom from the skin deformation incident capsule with no membrane but attached to the skin around its periphery

counterweighting there is freedom from the skin deformation incident capsule with no membrane but attached to the skin around its periphery A CELLULOID CAPSULE FOR MEASURING VENOUS PRESSURES By A. KROGH, A. H. TURNER IAD E. M. LANDIS 2 (From the Laboratory of Zoophysiology, University of Copenhagen, Copenhagen, Denmark) (Received for publication

More information

CHE 4115 Chemical Processes Laboratory 2 Experiment 1. Batch Distillation

CHE 4115 Chemical Processes Laboratory 2 Experiment 1. Batch Distillation CHE 4115 Chemical Processes Laboratory 2 Experiment 1 Batch Distillation BACKGROUND Distillation is one of the most commonly used unit operations in chemical engineering. In general, a distillation operation

More information

12. School travel Introduction. Part III Chapter 12. School travel

12. School travel Introduction. Part III Chapter 12. School travel 12. School travel 12.1 Introduction This chapter presents the evidence on changes in travel patterns for the journey to school in the three towns over the period of the Sustainable Travel Town project.

More information

THE literature on this subject, which was reviewed recently (CAMPBELL, doses of amytal, and in addition received A.C.E. mixture during the

THE literature on this subject, which was reviewed recently (CAMPBELL, doses of amytal, and in addition received A.C.E. mixture during the -~~ -v GAS TENSIONS IN THE MUCOUS MEMBRANE OF THE STOMACH AND SMALL INTESTINE. By J. ARGYLL CAMPBELL. From the National Institute for Medical Research, Hampstead. (With six figures in the text.) (Received

More information

THE BODY TEMPERATURE OF WOODLICE

THE BODY TEMPERATURE OF WOODLICE [2 7 I THE BODY TEMPERATURE OF WOODLICE BY E. B. EDNEY From the Zoology Department, University of Birmingham {Received 17 November 1950) (With Four Text-figures) INTRODUCTION The present work forms part

More information

Recitation question # 05

Recitation question # 05 Recitation and Lab # 05 The goal of this recitations / labs is to review material related to the CV and respiratory lectures for the second test of this course. Info required to answer this recitation

More information

A Fair Target Score Calculation Method for Reduced-Over One day and T20 International Cricket Matches

A Fair Target Score Calculation Method for Reduced-Over One day and T20 International Cricket Matches A Fair Target Score Calculation Method for Reduced-Over One day and T20 International Cricket Matches Rohan de Silva, PhD. Abstract In one day internationals and T20 cricket games, the par score is defined

More information

Deflate Gate : Preliminary Tests and Possible Science Explanations Introduction:

Deflate Gate : Preliminary Tests and Possible Science Explanations Introduction: Deflate Gate : Preliminary Tests and Possible Science Explanations Introduction: The following two preliminary tests were run to assess whether ball preparation and temperature would explain the deflate-gate

More information

reported that the pulmonary ventilation of a man could be predicted from his alveolar pco2 and deep body temperature, and anticipated that CO2 would

reported that the pulmonary ventilation of a man could be predicted from his alveolar pco2 and deep body temperature, and anticipated that CO2 would THE RESPIRATORY AND CARDIOVASCULAR RESPONSE TO IMMERSION IN COLD AND WARM WATER. By W. R. KEATINGE and M. EVANS. From the Department of Experimental Medicine, University of Cambridge. (Received for publication

More information

Objective To identify a pure liquid substance using the physical properties of solubility, density, and boiling point.

Objective To identify a pure liquid substance using the physical properties of solubility, density, and boiling point. Chemistry 1020 Identification of an Unknown Liquid Objective To identify a pure liquid substance using the physical properties of solubility, density, and boiling point. Text reference solubility, density,

More information

Homeostasis and Negative Feedback Concepts and Breathing Experiments 1

Homeostasis and Negative Feedback Concepts and Breathing Experiments 1 Homeostasis and Negative Feedback Concepts and Breathing Experiments 1 I. Homeostasis and Negative Feedback Homeostasis refers to the maintenance of relatively constant internal conditions. For example,

More information

Aerobic reoxidation in marine sediments

Aerobic reoxidation in marine sediments Aerobic reoxidation in marine sediments This exercise consists of three small experiments\demonstrations that should be run in parallel. Read the whole description and divide the work between the members

More information

Name. Lab Partners. The Dive Response. In this lab exercise, you will be designing and conducting your own experiments!

Name. Lab Partners. The Dive Response. In this lab exercise, you will be designing and conducting your own experiments! Name Lab Partners The Dive Response In this lab exercise, you will be designing and conducting your own experiments! Note: A formal report is due for this lab (see handout). Objectives 1. Characterize

More information

The physiological functions of respiration and circulation. Mechanics. exercise 7. Respiratory Volumes. Objectives

The physiological functions of respiration and circulation. Mechanics. exercise 7. Respiratory Volumes. Objectives exercise 7 Respiratory System Mechanics Objectives 1. To explain how the respiratory and circulatory systems work together to enable gas exchange among the lungs, blood, and body tissues 2. To define respiration,

More information

AP Biology Lab - Cell Respiration

AP Biology Lab - Cell Respiration AP Biology Lab - Cell Respiration This investigation uses respirometry techniques to calculate the rate of oxygen consumption (cellular respiration) in germinating pea seeds. The effect of temperature

More information

3 1 PRESSURE. This is illustrated in Fig. 3 3.

3 1 PRESSURE. This is illustrated in Fig. 3 3. P = 3 psi 66 FLUID MECHANICS 150 pounds A feet = 50 in P = 6 psi P = s W 150 lbf n = = 50 in = 3 psi A feet FIGURE 3 1 The normal stress (or pressure ) on the feet of a chubby person is much greater than

More information

BLOOD PRESSURE SENSOR 0377i

BLOOD PRESSURE SENSOR 0377i BLOOD PRESSURE SENSOR 0377i USER S GUIDE CENTRE FOR MICROCOMPUTER APPLICATIONS http://www.cma-science.nl Short description The Blood Pressure sensor 0377i is used to measure arterial blood pressure in

More information

The over-ventilated cat shows a similar adjustment to diminished. being over-ventilated, and he considered that on that account there was

The over-ventilated cat shows a similar adjustment to diminished. being over-ventilated, and he considered that on that account there was 6I2.235:6I2.26I THE SOURCE OF COa EXPIRED AND THE SITE OF ITS RETENTION. BY LAURENCE IRVING, J. K. W. FERGUSON AND F. B. PLEWES. (From the Department of Physiology, University of Toronto.) AFTER evisceration

More information

Douglas and Haldane(2) has shown that the oxygen determinations. since it forms the basis of the "Coefficient of Utilisation" (Krrogh) and

Douglas and Haldane(2) has shown that the oxygen determinations. since it forms the basis of the Coefficient of Utilisation (Krrogh) and THE MEASUREMENT OF THE OXYGEN CONTENT OF THE MIXED VENOUS BLOOD, AND OF THE VOLUME OF BLOOD CIRCULATING PER MINUTE. BY J. BARCROFT, F. J. W. ROUGHTON AND R. SHOJI. (From the Physiological Laboratory, Cambridge.)

More information

partial pressure is to be applied to the dissociation curve of fully oxygenated

partial pressure is to be applied to the dissociation curve of fully oxygenated 6I2. I27. I THE DETERMINATION OF THE CARBON DIOXIDE CONTENT OF THE MIXED VENOUS BLOOD. Part I. The effect of oxygenation and the critical oxygen tension. BY M. C. G. ISRAELS (Platt Physiological Scholar)

More information

Aug 17, 2001 LAB MANUAL MAXIMUM SPECIFIC GRAVITY (RICE VOIDS TEST) OF PAVING MIXTURES AASHTO Designation T 209 (Mn/DOT Modified))

Aug 17, 2001 LAB MANUAL MAXIMUM SPECIFIC GRAVITY (RICE VOIDS TEST) OF PAVING MIXTURES AASHTO Designation T 209 (Mn/DOT Modified)) Aug 17, 2001 LAB MANUAL 1807.0 1807 MAXIMUM SPECIFIC GRAVITY (RICE VOIDS TEST) OF PAVING MIXTURES AASHTO Designation T 209 (Mn/DOT Modified)) 1807.1 SCOPE This test method covers the determination of the

More information

Oxygen convulsions are believed by many workers to be caused by an accumulation

Oxygen convulsions are believed by many workers to be caused by an accumulation 272 J. Physiol. (I949) I09, 272-280 6I2.223.II:6I2.26I THE ROLE OF CARBON DIOXIDE IN OXYGEN POISONING BY H. J. TAYLOR From the Royal Naval Physiological Laboratory, Alverstoke, Hants (Received 26 March

More information

PRE LABORATORY ASSIGNMENT: Lab Section Score: /10 READ THE LAB TEXT BEFORE ATTEMPTING THESE PROBLEMS!

PRE LABORATORY ASSIGNMENT: Lab Section Score: /10 READ THE LAB TEXT BEFORE ATTEMPTING THESE PROBLEMS! EXPERIMENT # 6 Name: PRE LABORATORY ASSIGNMENT: Lab Section Score: /10 READ THE LAB TEXT BEFORE ATTEMPTING THESE PROBLEMS! 1. Calculate the height of a corresponding column of mercury (in mm) that is at

More information

ASTM D86 - Procedural Outline

ASTM D86 - Procedural Outline ASTM D86 - Procedural Outline Standard Test Method for Distillation of Petroleum Products and Liquid Fuels at Atmospheric Pressure The following summarizes the procedural steps required for performing

More information

University of Oxford. physiological relationship between them. However, oxygen consumption and

University of Oxford. physiological relationship between them. However, oxygen consumption and 144 J. Physiol. (I959) I49, I44-I53 BRATHING AND TH THRMAL NVIRONMNT IN YOUNG RABBITS BY K. ADAMSONS, JR.* From the Nuffield Institute for Medical Research, (Received 29 June 1959) University of Oxford

More information

AIRFLOW GENERATION IN A TUNNEL USING A SACCARDO VENTILATION SYSTEM AGAINST THE BUOYANCY EFFECT PRODUCED BY A FIRE

AIRFLOW GENERATION IN A TUNNEL USING A SACCARDO VENTILATION SYSTEM AGAINST THE BUOYANCY EFFECT PRODUCED BY A FIRE - 247 - AIRFLOW GENERATION IN A TUNNEL USING A SACCARDO VENTILATION SYSTEM AGAINST THE BUOYANCY EFFECT PRODUCED BY A FIRE J D Castro a, C W Pope a and R D Matthews b a Mott MacDonald Ltd, St Anne House,

More information

RESPIRATION OF MUSCLE. By W. M. FLETCHER, M.A., M.B., Fellow of Trinity College, Cambrtidge. (Three Figures

RESPIRATION OF MUSCLE. By W. M. FLETCHER, M.A., M.B., Fellow of Trinity College, Cambrtidge. (Three Figures THE INFLUENCE OF OXYGEN UPON THE SURVIVAL RESPIRATION OF MUSCLE. By W. M. FLETCHER, M.A., M.B., Fellow of Trinity College, Cambrtidge. (Three Figures in Text.) (From the Physiologial Laboratory, Cambridge.)

More information

Retinal vascular response to breathing increased carbon dioxide and oxygen concentrations. Regina Frayser and John B. Hickam

Retinal vascular response to breathing increased carbon dioxide and oxygen concentrations. Regina Frayser and John B. Hickam Retinal vascular response to breathing increased carbon dioxide and oxygen concentrations Regina Frayser and John B. Hickam The retina has a high rate of oxygen consumption, and the retinal vessels are

More information

11/22/ (4) Harmonization: <846> SPECIFIC SURFACE AREA

11/22/ (4) Harmonization: <846> SPECIFIC SURFACE AREA BRIEFING 846 Specific Surface Area, USP 27 page 2385. The European Pharmacopoeia is the coordinating pharmacopeia for the international harmonization of the Specific Surface Area General Chapter, as part

More information

Preliminary design of a high-altitude kite. A flexible membrane kite section at various wind speeds

Preliminary design of a high-altitude kite. A flexible membrane kite section at various wind speeds Preliminary design of a high-altitude kite A flexible membrane kite section at various wind speeds This is the third paper in a series that began with one titled A flexible membrane kite section at high

More information

of Carbon Dioxide (CO 2

of Carbon Dioxide (CO 2 CHAPTER 10 Phase Changes of Carbon Dioxide (CO 2 ) Objectives This experiment is an introduction to phase changes of pure substances and an introduction to some simple microtechniques for doing experiments

More information

The Variation of Muscle Oxygen Consumption With Velocity of Shortening

The Variation of Muscle Oxygen Consumption With Velocity of Shortening The Variation of Muscle Oxygen Consumption With Velocity of Shortening R.J. BASKIN From the Department of Zoology, University of California, Davis ABSTRACT Total oxygen consumption following contraction

More information

ATMOSPHERIC PRESSURE

ATMOSPHERIC PRESSURE ATMOSPHERIC PRESSURE 3.1 Air weight 3.2 Torricelli s experience 3.3 Pressure measuring unit 3.1 AIR WEIGHT Solid bodies have their own weight, and gaseous bodies such as air also have their own weight.

More information

Physical Chemistry of Gases: Gas Exchange Linda Costanzo, Ph.D.

Physical Chemistry of Gases: Gas Exchange Linda Costanzo, Ph.D. Physical Chemistry of Gases: Gas Exchange Linda Costanzo, Ph.D. OBJECTIVES: After studying this lecture, the student should understand: 1. Application of the gas laws to pulmonary physiology. 2. How to

More information

Respiration. Figure 22: Schematic representation of the respiratory system

Respiration. Figure 22: Schematic representation of the respiratory system Respiration One of the seven characteristics of something which is living is respiration. Strictly speaking, respiration is the process that takes place at cellular level and is one of three different

More information

From Bombe stops to Enigma keys

From Bombe stops to Enigma keys From Bombe stops to Enigma keys A remarkably succinct description of the Bombe written many years ago, reads as follows:- The apparatus for breaking Enigma keys, by testing a crib and its implications

More information

THE BIOLOGY OF THE PRAWN, PALAEMON

THE BIOLOGY OF THE PRAWN, PALAEMON J. mar. bio!. Ass. U.K. (1959) 38 621-627 Printed in Great Britain 621 THE BOLOGY OF THE PRAWN PALAEMON (=LEANDER) SERRA TU S (PENNANT) BY G. R. FORSTER The Plymouth Laboratory n a recent paper Cole (1958)

More information

of the Skin of Extremities

of the Skin of Extremities III. Oxygen Tension of Tissues by the Polarographic Method The Effect of Local Heat on the Oxygen Tension of the Skin of Extremities By ORVILLE HoRWITz, MI)., GEORGE PEIRCE, M.S., AND HUGH MONTGOMERY,

More information

HAP e-help. Obtaining Consistent Results Using HAP and the ASHRAE 62MZ Ventilation Rate Procedure Spreadsheet. Introduction

HAP e-help. Obtaining Consistent Results Using HAP and the ASHRAE 62MZ Ventilation Rate Procedure Spreadsheet. Introduction Introduction A key task in commercial building HVAC design is determining outdoor ventilation airflow rates. In most jurisdictions in the United States, ventilation airflow rates must comply with local

More information

ALVEOLAR - BLOOD GAS EXCHANGE 1

ALVEOLAR - BLOOD GAS EXCHANGE 1 ALVEOLAR - BLOOD GAS EXCHANGE 1 Summary: These notes examine the general means by which ventilation is regulated in terrestrial mammals. It then moves on to a discussion of what happens when someone over

More information

Gas Laws: Boyle s and Amonton s Laws Minneapolis Community and Technical College v.9.08

Gas Laws: Boyle s and Amonton s Laws Minneapolis Community and Technical College v.9.08 Gas Laws: Boyle s and Amonton s Laws Minneapolis Community and Technical College v.9.08 I. Introduction The purpose of this experiment is to test the extent real gases (to the limits of our measurements)

More information

Chapter 4: Ventilation Test Bank MULTIPLE CHOICE

Chapter 4: Ventilation Test Bank MULTIPLE CHOICE Instant download and all chapters Test Bank Respiratory Care Anatomy and Physiology Foundations for Clinical Practice 3rd Edition Will Beachey https://testbanklab.com/download/test-bank-respiratory-care-anatomy-physiologyfoundations-clinical-practice-3rd-edition-will-beachey/

More information

Circulation and Respiration: Vital Signs Student Version

Circulation and Respiration: Vital Signs Student Version Circulation and Respiration: Vital Signs Student Version In this lab, you will learn about the circulatory and respiratory systems. You will test the capacity of your lungs, measure your blood pressure

More information

GEOTHERMAL WELL COMPLETION TESTS

GEOTHERMAL WELL COMPLETION TESTS GEOTHERMAL WELL COMPLETION TESTS Hagen Hole Geothermal Consultants NZ Ltd., Birkenhead, Auckland, New Zealand. ABSTRACT This paper reviews the measurements that are typically made in a well immediately

More information

Respiratory Pulmonary Ventilation

Respiratory Pulmonary Ventilation Respiratory Pulmonary Ventilation Pulmonary Ventilation Pulmonary ventilation is the act of breathing and the first step in the respiratory process. Pulmonary ventilation brings in air with a new supply

More information

BLOOD PRESSURE SENSOR BT17i USER S GUIDE

BLOOD PRESSURE SENSOR BT17i USER S GUIDE BLOOD PRESSURE SENSOR BT17i USER S GUIDE CENTRE FOR MICROCOMPUTER APPLICATIONS http://www.cma-science.nl Short description The Blood Pressure sensor BT17i allows measuring arterial blood pressure. The

More information

VOLUNTARY BREATHHOLDING. I. PULMONARY GAS

VOLUNTARY BREATHHOLDING. I. PULMONARY GAS VOLUNTARY BREATHHOLDING. I. PULMONARY GAS EXCHANGE DURING BREATHHOLDING'1 By CHARLES D. STEVENS, EUGENE B. FERRIS, JOSEPH P. WEBB, GEORGE L. ENGEL, AND MYRTLE LOGAN (From the Departments of Internal Medicine

More information

Pulmonary Circulation

Pulmonary Circulation Pulmonary Circulation resin cast of pulmonary arteries resin cast of pulmonary veins Blood Flow to the Lungs Pulmonary Circulation Systemic Circulation Blood supply to the conducting zone provided by the

More information

Chapter 15 Fluids. Copyright 2010 Pearson Education, Inc.

Chapter 15 Fluids. Copyright 2010 Pearson Education, Inc. Chapter 15 Fluids Density Units of Chapter 15 Pressure Static Equilibrium in Fluids: Pressure and Depth Archimedes Principle and Buoyancy Applications of Archimedes Principle Fluid Flow and Continuity

More information

6833_INSTRUCTIONS MANUAL DIGITAL WIRST BLOOD PRESSURE

6833_INSTRUCTIONS MANUAL DIGITAL WIRST BLOOD PRESSURE 6833_INSTRUCTIONS MANUAL DIGITAL WIRST BLOOD PRESSURE PURCHASE ACKNOWLEDGEMENT JOCCA thanks you for the trust placed in the purchase of our product and we are certain that you will always be satisfied

More information

Exponent's Fundamentally Flawed Research

Exponent's Fundamentally Flawed Research Exponent's Fundamentally Flawed Research By Mike Greenway July 19, 2015 A fundamental flaw in Exponent's experiments invalidates their conclusion that the Patriot's deflated footballs. Many of Exponent's

More information

Inquiry Investigation: Factors Affecting Photosynthesis

Inquiry Investigation: Factors Affecting Photosynthesis Inquiry Investigation: Factors Affecting Photosynthesis Background Photosynthesis fuels ecosystems and replenishes the Earth's atmosphere with oxygen. Like all enzyme-driven reactions, the rate of photosynthesis

More information

Exploring the Properties of Gases

Exploring the Properties of Gases Computer 30 The purpose of this investigation is to conduct a series of experiments, each of which illustrates a different gas law. You will be given a list of equipment and materials and some general

More information

Calculating Total Uncertainty of Temperature Calibration with a Dry Block. Calibration White Paper. Beamex.

Calculating Total Uncertainty of Temperature Calibration with a Dry Block. Calibration White Paper. Beamex. Beamex Calibration White Paper info@beamex.com Calculating Total Uncertainty of Temperature Calibration with a Dry Block World-class calibration solutions Calculating Total Uncertainty of Temperature Calibration

More information

Tioga ISD Athletic Department Heat Policy

Tioga ISD Athletic Department Heat Policy Tioga ISD Athletic Department Heat Policy Practice of competition in hot and humid environmental conditions poses special problems for student-athletes. Heat stress and resulting heat illness is a primary

More information

Mitos Fluika Pressure and Vacuum Pumps Datasheet

Mitos Fluika Pressure and Vacuum Pumps Datasheet Unit 1, Anglian Business Park, Orchard Road, Royston, Hertfordshire, SG8 5TW, UK T: +44 (0)1763 242491 F: +44 (0)1763 246125 E: sales@dolomite-microfluidics.com W: www.dolomite-microfluidics.com Dolomite

More information

Objectives. Materials TI-73 CBL 2

Objectives. Materials TI-73 CBL 2 . Objectives Activity 18 To model the cooling rate of different sizes of animals To determine the effect of skin surface area on the cooling rate of animals Materials TI-73 Body Cooling Rate of Animals

More information

Projections of road casualties in Great Britain to 2030

Projections of road casualties in Great Britain to 2030 5 Projections of road casualties in Great Britain to 2030 C G B (Kit) Mitchell and R E Allsop Published March 2014 Contents Section 1 Introduction 4 Section 2 Trends in road casualty rates 6 Section 3

More information

G622. APPLIED SCIENCE Monitoring the Activity of the Human Body ADVANCED SUBSIDIARY GCE. Thursday 27 May 2010 Afternoon. Duration: 1 hour 30 minutes

G622. APPLIED SCIENCE Monitoring the Activity of the Human Body ADVANCED SUBSIDIARY GCE. Thursday 27 May 2010 Afternoon. Duration: 1 hour 30 minutes ADVANCED SUBSIDIARY GCE APPLIED SCIENCE Monitoring the Activity of the Human Body G622 *OCE/17533* Candidates answer on the Question Paper OCR Supplied Materials: None Other Materials Required: Electronic

More information

Calcimeter Instruction Manual

Calcimeter Instruction Manual Hohner (UK - Canada - Texas) Calcimeter Instruction Manual The Hohner Calcimeter is based on industry standard versions, and is used to measure the calcium carbonate and magnesium carbonate in samples.

More information

Laboratory practice. Preparation and use of an ice point bath as a reference temperature. Document number TE-LP-001. Version: 07

Laboratory practice. Preparation and use of an ice point bath as a reference temperature. Document number TE-LP-001. Version: 07 Approval and Calibration Services Laboratory technical manual Laboratory practice Preparation and use of an ice point bath as a reference temperature Document number TE-LP-001 Version: 07 File name: TE-LP-001

More information

Runs Solution Temp. Pressure zero reset

Runs Solution Temp. Pressure zero reset IAEA-SM-367/8/02/P High Quality Tank Calibration Study JSGO H.Higuchi, S.Takeda NMCC--S. Uchikoshi, Y. Watanabe, K. Kaieda IAEA--D. Sellinschegg, R.Binner 1. INTRODUCTION: The Japanese Nuclear Material

More information