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1. The microvasculature of the lung of the duck and pigeon was studied by scanning electron microscopy of vascular casts and critical point dried preparations of the gas exchange tissue. 2. The gas-exchange cappilaries are discrete tubular vessels intimately associated with air capillaries in a three dimensional network. 3. The capillaries originate from arteries at the periphery of the parabronchus, and are collected by veins which run close to its luminal surface. 4. The capillary bed of 3-5 atria is drained by a single vein. It is suggested that the vein and its associated capillaries may form a controllable subunit of pulmonary perfusion.

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The normal pattern of breathing movements in Rana pipiens has been studied by recording pressure and volume changes in the buccal cavity and lungs, and electromyograms from the muscles involved in this activity. Two types of breathing movement were obtained, one concerned with ventilation of the buccal cavity (buccal cycles) and the other with lung ventilation (lung cycles). Only in the latter type of movement were the nares and glottis actively involved. During buccal cycles the nares remained open and the glottis closed, so although excursions of the buccal floor were some two-thirds of the magnitude of those occurring during lung cycles, only low pressures were generated. The onset of a lung cycle was signalled by activity in the laryngeal dilator muscle. When the glottis opened, lung pressure and volume decreased, and buccal cavity pressure and volume increased. After closure of the nares, the buccal floor was rapidly elevated by the activity of the breathing muscles and air was forced into the lungs from the buccal cavity. At peak pressure in the lungs and buccal cavity the glottis closed and nares opened. The recovery stroke of the buccal pump was passive. No evidence was found for large pressure differentials between the buccal cavity and lungs when the glottis was open, and air-flow recordings at the external nares showed two phases of flow during each buccal cycle and four phases with each lung ventilation cycle.

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Heart rate and breathing movements have been monitored in three unrestrained harbor seals. On voluntary submergence heart rate fell markedly in all seals, and after 2–3 s submergence stabilized at about 40–50% of the predive level. Heart rate increased before the animals broke surface at the end of the dive and, when breathing began again, a postdive tachycardia was observed. Two of the three seals frequently showed anticipation of the dive as judged from their heart-rate response. Heart rate during feeding dives was generally more variable; in fact one seal exhibited no bradycardia in 20% of its feeding dives, although another seal showed a significantly greater bradycardia than was seen in routine dives. When breathing rate was low (less than five breaths min−1) respiratory variations in the heart rate occurred, although the onset of bradycardia was much more rapid during diving than during breath-holding. Because of the flexibility of the response it is concluded that the generation of diving bradycardia in the seal is a complex phenomenon which, aside from any responses set in train by peripheral receptors, must also involve some form of associative learning.

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