Birds have the parts of the brain formed and arranged in a way that is equally distinctive. The cerebral lobes are relatively large and convex, and deserve the descriptive name "hemispheres." They are always smooth, as among the lower Mammals, and extend backward so as to abut against the hind brain, termed the cerebellum. This junction is brought about in a peculiar way. The cerebral hemispheres in a bird do not extend backward to override the optic lobes, and hide them, as occurs among adult mammals, but they extend back between the optic lobes, so as to force them apart and push them aside, downward and backward, till they extend laterally beyond the junction of the cerebrum with the cerebellum. The brain of a Bird is never reptilian; but in the young Mammal the brain has a very reptilian aspect, because both have their parts primarily arranged in a line. Therefore the brain appears to determine the boundary between bird and reptile exactly.
REPTILIAN BREATHING ORGANS
The breathing organs of Birds and Reptiles which are associated with these different types of brain are not quite the same. The Frog has a cellular lung which, in the details of the minute sacs which branch and cluster at the terminations of the tubes, is not unlike the condition in a Mammal. In a mammal respiration is aided by the bellows-like action of the muscles connected with the ribs, which encase the cavity where the lungs are placed, and this structure is absent in the Frog and its allies. The Frog, on the other hand, has to swallow air in much the same way as man swallows water. The air is similarly grasped by the muscles, and conveyed by them downward to the lungs. Therefore a Frog keeps its mouth shut, and the animal dies from want of air if its mouth is open for a few minutes.
Crocodiles commonly lie in the sun with their mouths widely open. The lungs in both Crocodiles and Turtles are moderately dense, traversed by great bronchial tubes, but do not differ essentially in plan from those of a Frog, though the great branches of the bronchial tubes are stronger, and the air chambers into which the lung is divided are somewhat smaller. The New Zealand Hatteria has the lungs of this cellular type, though rather resembling the amphibian than the Crocodile. The lungs during life in all these animals attain considerable size, the maximum dimensions being found in the terrestrial tortoises, which owe much of their elevated bulk to the dimensions of the air cells which form the lungs.
The lungs of Serpents and Lizards are formed on a different plan. In both those groups of reptiles the dense cellular tissue is limited to the part of the lung which is nearest to the throat. This network of blood vessels and air cells extends about the principal bronchial tube much as in other animals, but as it extends backward the blood vessels become few until the tubular lung appears in its hinder part, as it extends down the body, almost as simple in structure as the air bladder of a fish. Among Serpents only one of these tubular lungs is commonly present, and the structure has a less efficient appearance as a breathing organ than the single lung of the fish Ceratodus ([Fig. 1]). The Chameleons are a group of lizards which differ in many ways from most of their nearest kindred, and the lungs, while conforming in general plan to the lizard type in being dense at the throat, and a tubular bladder in the body, give off on both sides a number of short lateral branches like the fingers of a glove ([Fig. 18, p. 51]).
Thus the breathing organs of reptiles present two or three distinct types which have caused Serpents and Lizards to be associated in one group by most naturalists who have studied their anatomy; while Crocodiles and Chelonians represent a type of lung which is quite different, and in those groups has much in common. These characters of the breathing organs contribute to separate the cold-blooded armoured reptiles from the warm-blooded birds clothed with feathers, as well as from the warm-blooded mammals which suckle their young; for both these higher groups have denser and more elastic spongy lung tissue.
It will be seen hereafter that many birds in the most active development of their breathing organs substantially revert to the condition of the Serpent or Chameleon in a somewhat modified way. Because, instead of having one great bronchial tube expanded to form a vast reservoir of air which can be discharged from the lung in which the reptile has accumulated it, the bird has the lateral branches of the bronchial tubes prolonged so as to pierce the walls of the lung, when its covering membrane expands to form many air cells, which fill much of the cavity of the bird's body (see [Fig. 16]). Thus the bird appears to combine the characters of such a lung as that of a Crocodile, with a condition which has some analogy with the lung of a Chameleon. It is this link of structure of the breathing organs between reptiles and birds that constitutes one of the chief interests of flying reptiles, for they prove to have possessed air cells prolonged from the lungs, which extended into the bones.