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Dragons of the Air

<h2>CHAPTER VIII THE PLAN OF THE SKELETON</h2> While these animals are incontestably nearer to birds than to any other animals in their plan of organisation, thus far no proof has been found that they are birds, or can be included in the same division of vertebrate life with feathered animals. It is one of the oldest and soundest teachings of Linnæus that a bird is known by its feathers; and the record is a blank as to any covering to the skin in Pterodactyles. There is the strongest probability against feathers having existed such as are known in the Archæopteryx, because every Solenhofen Ornithosaur appears to have the body devoid of visible or preservable covering, while the two birds known from the Solenhofen Slate deposit are well clothed with feathers in perfect preservation. We turn from the skin to the skeleton. The plan on which the skeleton is constructed remains as evidence of the animal's place in nature, which is capable of affording demonstration on which absolute reliance would have been placed, if the brain and pneumatic foramina had remained undiscovered. With the entire skeleton before us, it is inconceivable that anatomical science should fail to discover the[Pg 59] true nature of the animal to which it belonged, by the method of comparing one animal with another. There is no lack of this kind of evidence of Pterodactyles in the three or four scores of skeletons, and thousands of isolated or associated bones, preserved in the public museums of Europe and America. I may recall the circumstance that the discovery of skeletons of fossil animals has occasionally followed upon the interpretation of a single fragment, from which the animal has been well defined, and sometimes accurately drawn, before it was ever seen. So I propose, before drawing any conclusions from the skeletons in the entirety of their construction, to examine them bone by bone, and region by region, for evidence that will manifest the nature of this brood of Dragons. Their living kindred, and perhaps their extinct allies, assembled as a jury, may be able to determine whether resemblances exist between them, and whether such similarity between the bones as exists is a common inheritance, or is a common acquisition due to similar ways of life, and no evidence of the grade of the organism among vertebrate animals. The bones of these Ornithosaurs, when found isolated, first have to be separated from the organisms with which they are associated and mixed in the geological strata. This discrimination is accomplished in the first instance by means of the texture of the surface. The density and polish of the bones is even more marked than in the bones of birds, and is usually associated with a peculiar thinness of substance of the bone, which is comparable to the condition in a bird, though usually a little stouter, so that the bones resist crushing better. Pterodactyle[Pg 60] bones in many instances are recognised by their straightness and comparatively uniform dimensions, due to the exceptional number of long bones which enter into the structure of the wing as compared with birds. When the bones are unerringly determined as Ornithosaurian, they are placed side by side with all the bones which are most like them, till, judged by the standard of the structures of living animals, the fossil is found to show a composite construction as though it were not one animal but many, while its individual bones often show equally composite characters, as though parts of the corresponding bone in several animals had been cunningly fitted together and moulded into shape. <h4>THE PLAN OF THE HEAD IN ORNITHOSAURS</h4> The head is always the most instructive part of an animal. It is less than an inch long in the small Solenhofen skeleton named Pterodactylus brevirostris, and is said to be three feet nine inches long in the toothless Pterodactyle Ornithostoma from the Chalk of Kansas. Most of these animals have a long, slender, conical form of head, tapering to the point like the beak of a Heron, forming a long triangle when seen from above or from the side. Sometimes the head is depressed in front, with the beak flattened or rounded as in a Duck or Goose, and occasionally in some Wealden and Greensand species the jaws are truncated in front in a massive snout quite unlike any bird. The back of the head is sometimes rounded as among birds, showing a smooth pear-shaped posterior convexity in the region of the brain. Sometimes the back of the head is square and vertical or oblique. Occasionally a great crest of cellular[Pg 61] tissue is extended backward from above the brain case over the spines of the neck bones. There are always from two to four lateral openings in the skull. First, the nostril is nearest to the extremity of the beak. Secondly, the orbits of the eyes are placed far backward. These two openings are always present. The nostril may incline upward. The orbits of the eyes are usually lateral, though their upper borders sometimes closely approximate, as in the woodpecker-like types from the Solenhofen Slate named Pterodactylus Kochi, now separated as another genus. In most genera there is an opening in the side of the head, between the eye hole and the nostril, known as the antorbital vacuity; and another opening, which is variable in size and known as the temporal vacuity, is placed behind the eye. The former is common in the skulls of birds, the latter is absent from all birds and found in many reptiles. The palate is usually imperfectly seen, but English and American specimens have shown that it has much in common with the palate in birds, though it varies greatly in form of the bones in representatives from the Lias, Oolites, and Cretaceous rocks. From the scientific aspect the relative size of the head, its form, and the positions and dimensions of its apertures and processes, are of little importance in comparison with its plan of construction, as evidenced by the positions and relations to each other of the bones of which it is formed. There usually is some difficulty in stating the limits of the bones of the skull, because in Pterodactyles, as among birds, they usually blend together, so that in the adult animal the sutures between the bones are commonly obliterated.[Pg 62] Bones have relations to each other and places in the head which can only change as the organs with which they are associated change their positions. No matter what the position of a nostril may be—at the extremity of a long snout, as in an ant-eater, or far back at the top of the head in a porpoise, or at the side of the head in a bird—it is always bordered by substantially the same bones, which vary in length and size with the changing place of the nostril and the form of the head. Every region of the head is defined by this method of construction; so that eye holes and nose holes, brain case and jaw bones, palate and teeth, beak, and back of the skull are all instructive to those who seek out the life-history of these animals. We may briefly examine the head of an Ornithosaurian. <h4>BONES ABOUT THE NOSTRIL</h4> No matter what its form may be, the head of an Ornithosaur always terminates in front in a single bone called the intermaxillary. It sends a bar of bone backward above the visible nostrils, between them; and a bar on each side forms the margin of the jaw in which teeth are implanted. The bone varies in depth, length, sharpness, bluntness, slenderness, and massiveness. As the bone becomes long the jaw is compressed from side to side, and the openings of the nostrils are removed backward to an increasing distance from the extremity of the beak. The outer and hinder border of the nostril is made by another bone named the maxillary bone, which is usually much shorter than the premaxillary. It contains the hindermost teeth, which rarely differ [Pg 63] from those in front, except in sometimes being smaller. The nasal bones, which always make the upper and hinder border of the nostrils, meet each other above them, in the middle line of the beak. <div class="figcenter"> FIG. 20 <ANTIMG src="images/i_080.jpg" width-obs="594" height-obs="480" alt="FIG. 20" title="FIG. 20" /> Showing that the extremity of the jaws in Rhamphorhynchus was sheathed in horn as in the giant Kingfisher, since the jaws similarly gape in front. The hyoid bones are below the lower jaw in the Pterodactyle. </div> The nostrils are unusually large in the Lias genus named Dimorphodon, and small in species of the genus Rhamphorhynchus from Solenhofen. Such differences result from the relative dimensions and proportions of these three bones which margin the nasal vacuity, and by varying growth of their front margins or of their hinder margins govern the form of the snout. The jaws are most massive in the genera known from the Wealden beds to the Chalk. The palatal surface is [Pg 64] commonly flat or convex, and often marked by an elevated median ridge which corresponds to a groove in the lower jaw, though the median ridge sometimes divides the palate into two parallel concave channels. The jaw is margined with teeth which are rarely fewer than ten or more than twenty on each side. They are sharp, compressed from side to side, curved inward, and never have a saw-like edge on the back and front margins. No teeth occur upon the bones of the palate. In most birds there is a large vacuity in the side of the head between the nostril and the orbit of the eye, partly separated from it by the bone which carries the duct for tears named the lachrymal bone. The same preorbital vacuity is present in all long-tailed Pterodactyles, though it is either less completely defined or absent in the group with short tails. It affords excellent distinctive characters for defining the genera. In the long-tailed genus Scaphognathus from Solenhofen this preorbital opening is much larger than the nostril, while in Dimorphodon these vacuities are of about equal size. Rhamphorhynchus is distinguished by the small size of the antorbital vacuity, which is placed lower than the nostril on the side of the face. The aperture is always imperfectly defined in Pterodactylus, and is a relatively small vacuity compared with the long nostril. In Ptenodracon the antorbital vacuity appears to have no existence separate from the nostril which adjoins the eye hole. And so far as is known at present there is no lateral opening in advance of the eye in the skull in any Ornithosaur from Cretaceous rocks, though the toothless Ornithostoma is the only genus with the skull complete. When a separate [Pg 65] antorbital vacuity exists, it is bordered by the maxillary bone in front, and by the malar bone behind. The prefrontal bone is at its upper angle. That bone is known in a separate state in reptiles and, I think, in monotreme mammals. Its identity is soon lost in the mammal, and its function in the skull is different from the corresponding bone in Pterodactyles. <h4>BONES ABOUT THE EYES</h4> <div class="figcenter"> FIG. 21.   UPPER SURFACE OF SKULL OF THE HERON Compared with the same aspect of the skull of Rhamphorhynchus <ANTIMG src="images/i_082.jpg" width-obs="492" height-obs="480" alt="FIG. 21." title="FIG. 21." /></div> The third opening in the side of the head, counting from before backward, is the orbit of the eye. In this vacuity is often seen the sclerotic circle of overlapping bones formed in the external membrane of the eye, like those in nocturnal birds and some reptiles. The [Pg 66] eye hole varies in form from an inverted pear-shape to an oblique or transverse oval, or a nearly circular outline. It is margined by the frontal bone above; the tear bone or lachrymal, and the malar or cheek bone in front; while the bones behind appear to be the quadrato-jugal and post-frontal bones, though the bones about the eye are somewhat differently arranged in different genera. The eyes were frequently, if not always, in contact with the anterior walls of the brain case, as in many birds, and are always far back in the side of the head. In Dimorphodon they are in front of the articulation of the lower jaw; in Rhamphorhynchus, above that articulation; while in Ornithostoma they are behind the articulation for the jaw. This change is governed by the position of the quadrate bone, which is vertical in the Lias genus, inclined obliquely forward in the fossils from the Oolites, and so much inclined in the Chalk fossil that the small orbit is thrown relatively further back. Thus far the chief difference in the Pterodactyle skull from that of a bird is in the way in which the malar arch is prolonged backward on each side. It is a slender bar of bone in birds, without contributing ascending processes to border vacuities in the side of the face, while in these fossil animals the lateral openings are partly separated by the ascending processes of these bones. This divergence from birds, in the malar bone entering the orbit of the eye is approximated to among reptiles and mammals, though the conditions, and perhaps the presence of a bone like the post-orbital bone, are paralleled only among Reptiles. The Pterodactyles differ among themselves enough for the head to make a near [Pg 67] approach to Reptiles in Dimorphodon, and to Birds in Pterodactylus. In the Ground Hornbill and the Shoebill the lachrymal bones in front of the orbits of the eyes grow down to meet the malar bars without uniting with them. The post-frontal region also is prolonged downward almost as far as the malar bar, as though to show that a bird might have its orbital circle formed in the same way and by the same bones as in Pterodactylus. Cretaceous Ornithosaurs sometimes differ from birds apparently in admitting the quadrato-jugal bone into the orbit. It then becomes an expanded plate, instead of a slender bar as in all birds. <h4>THE TEMPORAL FOSSA</h4> A fourth vacuity is known as the temporal fossa. When the skull of such a mammal as a Rabbit, or Sheep, is seen from above, there is a vacuity behind the orbits for the eyes, which in life is occupied by the muscles which work the lower jaw. It is made by the malar bone extending from the back of the orbit and the process of bone, called the zygomatic process, extending forward from the articulation of the jaw, which arches out to meet the malar bone. In birds there is no conspicuous temporal fossa, because the malar bar is a slender rod of bone in a line with the lower end of the quadrate bone. Reptile skulls have sometimes one temporal vacuity on each side, as among tortoises, formed by a single lateral bar. These vacuities, which correspond to those of mammals in position, are seen from the top of the head, as lateral vacuities behind the orbits of the eyes, and are termed superior temporal vacuities. In addition to these there is often in other [Pg 68] reptiles a lateral opening behind the eye, termed the inferior temporal vacuity, seen in Crocodiles, in Hatteria, and in Lizards; and in such skulls there are two temporal bars seen in side view, distinguished as superior and inferior. The superior arch always includes the squamosal bone, which is at the back of the single bar in mammals. The lower arch includes the malar bone, which is in front in the single arch of mammals. The circumstance that both these arches are connected with the quadrate bone makes the double temporal arch eminently reptilian. In Ornithosaurs the lateral temporal vacuity varies from a typically reptilian condition to one which, without becoming avian, approaches the bird type. In skulls from the Lias, Dimorphodon and Campylognathus, there is a close parallel to the living New Zealand reptile Hatteria, in the vertical position of the quadrate bone and in the large size of the vacuity behind and below the eye, which extends nearly the height of the skull. In the species of the genus Pterodactylus, the forward inclination of the quadrate bone recalls the Curlew, Snipe, and other birds. The back of the head is rounded, and the squamosal bone, which appears to enter into the wall of the brain case as in birds and mammals, is produced more outward than in birds, but less than in mammals, so as to contribute a little to the arch which is in the position of the post-frontal bone of reptiles. It is triangular, and stretches from the outer angle of the frontal bone at the back of the orbit to the squamosal behind, where it also meets the quadrate bone. Its third lower branch meets the quadratojugal, which rests upon the front of the quadrate bone, as in Iguanodon, and is unlike Dimorphodon [Pg 69] in its connexions. In that genus the supra-temporal bone, or post-orbital bone, appears to rest upon the post-frontal and connect it with the quadrato-jugal. In Dimorphodon the malar bone is entirely removed from the quadrate, but in Pterodactylus it meets its articular end. Between the post-frontal bone above and the quadrato-jugal bone below is a small lunate opening, which represents the lateral temporal vacuity; and so far, this is a reptilian character. But if the thin post-frontal bone were absorbed, Pterodactylus would resemble birds. There is no evidence that the quadrate bone is free in any Ornithosaurs, as it is in all birds, while in Dimorphodon it unites by suture with the squamosal bone. In Ornithostoma the lateral temporal vacuity is little more than a slit between the quadrate bone below, the quadrato-jugal in front, and what may be the post-frontal bone behind (see Fig. 2, p. 12). <h4>BONES ABOUT THE BRAIN</h4> The bones containing the brain appear to be the same as form the brain case in birds. The form of the back of the skull varies in two ways. First it may be flat above and flat at the back, when the back of the head appears to be square. This condition is seen in all the long-tailed genera, such as Campylognathus from the Lias and Rhamphorhynchus, and is associated with a high position for the upper temporal bar. Secondly, the back of the head may be rounded convexly, both above and behind. That condition is seen in the short-tailed genera, such as Pterodactylus. But in the large Cretaceous types, such as Ornithocheirus and Ornithostoma, the superior longitudinal ridge which runs back in [Pg 70] the middle line of the face becomes elevated and compressed from side to side at the back of the head as a narrow deep crest, prolonged backward over the neck vertebræ for some inches of length. All these three types are paralleled more or less in birds which have the back of the head square like the Heron, or rounded like the Woodpecker; or crested, though the crest of the Cormorant is not quite identical with Ornithocheirus, being a distinct bone at the back of the head in the bird which never blends with the skull. In so far as the crest is reptilian it suggests the remarkable crest of the Chameleon. In the structure of the back of the skull the bones are a modification of the reptilian type of Hatteria in the Lias genus Campylognathus, but the reptilian characters appear to be lost in the less perfectly preserved skulls of Cretaceous genera. The palate is well known in the chief groups of Ornithosaurs, such as Campylognathus, Scaphognathus, and Cycnorhamphus. Mr. E. T. Newton, F.R.S., has shown that in the English skull from the Lias of Whitby, the forms of the bones are similar to the palate in birds and unlike the conditions in reptiles. There is one feature, however, which may indicate a resemblance to Dicynodon and other fossil reptiles from South Africa. A slender bone extends from the base of the brain case, named the basi-sphenoid bone, outward and forward to the inner margin of the quadrate bone (Fig. 22). A bone is found thus placed in those South African Reptiles, which show many resemblances to the Monotreme and Marsupial Mammals. It is not an ordinary element of the skeleton and is unknown in living animals of any kind in that position. It has been [Pg 71] thought possible that it may represent one of the bones which among mammals are diminutive and are included in the internal ear. The resemblance may have some interest hereafter, as helping to show that certain affinities of the Ornithosaurs may lie outside the groups of existing reptiles. Instead of being directed transversely outward, as in the palatal region of Dicynodon lacerticeps, they diverge outward and forward to the inner border of the articulation for the lower jaw which is upon the quadrate bone. <div class="figcenter"> FIG. 22 <ANTIMG src="images/i_088.jpg" width-obs="635" height-obs="480" alt="FIG. 22" title="FIG. 22" /></div> <h4>BONES OF THE PALATE</h4> There is a pair of bones which extend forward from these inner articular borders of the quadrate bones, and converge in a long V-shape till they merge in the hard palate formed by the bones of the front of the beak, named intermaxillary and maxillary bones. The limits of the bones of the palate are[Pg 72] not distinct, but there can be no doubt that the front of the V is the bone named vomer, that the palatine bones are at its sides, and that its hinder parts are the pterygoid bones as in birds. There is a long, wide, four-sided, open space in the middle of the palate, between the vomer and the basi-sphenoid bone, unlike anything in birds or other animals. Professor Marsh, in a figure of the palate in the great skull of the toothless Pterodactyle named Ornithostoma (Pteranodon), from the Chalk of Kansas, found a large oval vacuity in this region of the palate. In that genus the pterygoid bones meet each other between the quadrate bones as in Dicynodon (Fig. 73, p. 182). Hence the great palatal vacuity here seen in the Ornithosaur is paralleled by the small vacuity in the South African reptile, which is sometimes distinct and sometimes partly separated from the anterior part of the vacuity which forms the openings of the nostrils on the palate. The Solenhofen skulls which give any evidence of the palate are exposed in side view only, and the bones, imperfectly seen through the lateral vacuities, are displaced by crushing. They include long strips like the vomerine bones in the Lias fossil, and they diverge in the same way as they extend back to the quadrate bones. The oblique division into vomer in front and pterygoid bone behind is shown by Goldfuss in his original figure of Scaphognathus. Thus there is some reason for believing that all Ornithosaurs have the palate formed upon the same general plan, which is on the whole peculiar to the group, especially in not having the palatal openings of the nares divided in the middle line. It would appear probable that the short-tailed animals have the pterygoid bones[Pg 73] meeting in the middle line and triangular; and that they are slender rods entirely separate from each other in the long-tailed genera. <h4>THE TEETH</h4> The teeth are all of pointed, elongated shape, without distinction into the kinds seen in most mammals and named incisors, canines, and grinders. They are organs for grasping, like the teeth of the fish-eating Crocodile of India, and are not unlike the simple teeth of some Porpoises. They are often implanted in oblique oval sockets with raised borders, usually at some distance apart from each other, and have the crown pointed, flattened more on the outer side than on the inner side, usually directed forward and curved inward. As in many extinct animals allied to existing reptiles, the teeth are reproduced by germs, which originate on the inner side of the root and grow till they gradually absorb the substance of the old tooth, forming a new one in its place. Frequently in Solenhofen genera, like Scaphognathus and Pterodactylus, the successional tooth is seen in the jaw on the hinder border of the tooth in use. There is some variation in the character of bluntness or sharpness of the crowns in the different genera, and in their size. The name Dimorphodon, given to the animal from the Lias of Lyme Regis, expresses the fact that the teeth are of two kinds. In the front of the jaw three or four large long teeth are found in the intermaxillary bone on each side, as in some Plesiosaurs, while the teeth found further back in the maxillary bone are smaller, and directed more vertically downward. This difference is more marked in the lower jaw than in the upper jaw. In Rhamphorhynchus the teeth are all[Pg 74] relatively long and large, and directed obliquely forward, but absent from the extremities of the beak, as in the German genus from the Lias named Dorygnathus, in which the bone of the lower jaw (which alone is known) terminates in a compressed spear. In Scaphognathus the teeth are few, more vertical, and do not extend backward so far as in Rhamphorhynchus, but are carried forward to the extremity of the blunt, deep jaw. In the short-tailed Pterodactyles the teeth are smaller, shorter, wider at the base of the crown, closer together, and do not extend so far backward in the jaw. In Ornithocheirus two teeth always project forward from the front of the jaw. Ornithostoma is toothless. <h4>SUPPOSED HORNY BEAK</h4> Sometimes a horny covering has been suggested for the beak, like that seen in birds or turtles, but no such structure has been preserved, even in the Solenhofen Slate, in which such a structure would seem as likely to be preserved as a wing membrane, though there is one doubtful exception. There are marks of fine blood vessels on some of the jaws, indicating a tough covering to the bone. In Rhamphorhynchus the jaws appear to gape towards their extremities as though the interspace had originally been occupied by organic substance like a horny beak. <h4>LOWER JAW</h4> The lower jaw varies in relative length with the vertical or horizontal position of the quadrate bone in the skull. In Dimorphodon the jaw is as long as the skull; but in the genera from the Oolitic rocks the[Pg 75] mandible is somewhat shorter, and in Ornithostoma the discrepancy reaches its maximum. The hinder part of the jaw is never prolonged backward much beyond the articulation, differing in this respect from Crocodiles and Plesiosaurs. The depth of the jaw varies. It is slender in Pterodactylus, and is probably stronger relatively to the skull in Scaphognathus than in any other form. It fits between the teeth and bones of the alveolar border in the skull, in all the genera. In Dimorphodon its hinder border is partly covered by the descending edge of the malar process which these animals develop in common with some Dinosaurs, and some Anomodont reptiles, and many of the lower mammals. In this hinder region the lower jaw is sometimes perforated, in the same way as in Crocodiles. That condition is observed in Dimorphodon, but is not found in Pterodactylus. The lower jaw is always composite, being formed by several bones, as among reptiles and birds. The teeth are in the dentary bone or bones, and these bones are almost always blended as in most birds and Turtles, and not separate from each other as among Crocodiles, Lizards, and Serpents. An interesting contour for the lower border of the jaw is seen in Ornithostoma, as made known in figures of American examples by Professors Marsh and Williston. It deepens as it extends backwards for two-thirds its length, stops at an angle, and then the depth diminishes to the articulation with the skull. This angle of the lower jaw is a characteristic feature of the jaws of Mammals. It is seen in the monotreme Echidna, and is characteristic of some Theriodont Reptiles from South Africa, which in [Pg 76] many ways resemble Mammals. The character is not seen in the jaws of specimens from the Oolitic rocks, but is developed in the toothed Ornithocheirus from the Cambridge Greensand, and is absent from the jaws of existing reptiles and birds. <div class="figcenter"> FIG. 23.   COMPARISON OF THE LOWER JAW IN ECHIDNA AND ORNITHOSTOMA <ANTIMG src="images/i_093.jpg" width-obs="640" height-obs="417" alt="FIG. 23." title="FIG. 23." /></div> <h4>SUMMARY OF CHARACTERS OF THE HEAD</h4> Taken as a whole, the head differs from other types of animals in a blending of characters which at the present day are found among Birds and Reptiles, with some structures which occur in extinct groups of animals with similar affinities, and perhaps a slight indication of features common to the lowest mammals. It is chiefly upon the head that the diverse views of earlier writers have been based. Cuvier was impressed with the reptilian aspect of the teeth; but in later times discoveries were made of Birds with teeth—Archæopteryx, Ichthyornis, Hesperornis. The teeth are quite reptilian, being not unlike miniature teeth [Pg 77] of Mosasaurus. If those birds had been found prior to the discovery of Pterodactyles, the teeth might have been regarded as a link with the more ancient birds, rather than a crucial difference between birds and reptiles. All the specimens show a lateral temporal hole in the bones behind the eye, and this is found in no bird or mammal, and is typical of such reptiles as Hatteria. The quadrate bone may not be so decisive as Cuvier thought it to be, for its form is not unlike the quadrate of a bird, and different, so far as I have seen, from that of living reptiles. This region of the head is reptilian, and if it occurred in a bird the character would be as astonishing as was the discovery of teeth in extinct birds. These characters of the head are also found in fossil animals named Dinosaurs, in association with many resemblances to birds in their bones. The palate might conceivably be derived from that of Hatteria by enlarging the small opening in the middle line in that reptile till it extended forward between the vomera; but it is more easily compared with a bird, which the animal resembles in its beak, and in the position of the nares. Excepting certain Lizards, all true existing Reptiles have the nostrils far forward and bordered by two premaxillary bones instead of one intermaxillary, as in Birds and Ornithosaurs. If nothing were known of the animal but its head bones, it would be placed between Reptiles and Birds. <hr style="width: 65%;" /> [Pg 78] <div style="break-after:column;"></div>

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