Reptiles and Birds

The amniotes—reptiles, birds, and mammals—are distinguished from amphibians by their terrestrially adapted (shelled) egg and an embryo protected by amniotic membranes. The evolution of amniotic membranes meant that the embryos of amniotes could develop within an aquatic environment inside the egg. This led to less dependence on a water environment for development and allowed the amniotes to invade drier areas. This was a significant evolutionary change that distinguished them from amphibians, which were restricted to moist environments due to their shell-less eggs. Although the shells of various amniotic species vary significantly, they all allow retention of water. The membranes of the amniotic egg also allowed gas exchange and sequestering of wastes within the enclosure of an eggshell. The shells of bird eggs are composed of calcium carbonate and are hard and brittle, but possess pores for gas and water exchange. The shells of reptile eggs are more leathery and pliable. Most mammals do not lay eggs; however, even with internal gestation, amniotic membranes are still present.

In the past, the most common division of amniotes has been into classes Mammalia, Reptilia, and Aves. Birds are descended, however, from dinosaurs, so this classical scheme results in groups that are not true clades. We will discuss birds as a group distinct from reptiles with the understanding that this does not reflect evolutionary history.

Reptiles

Reptiles are tetrapods. Limbless reptiles—snakes—may have vestigial limbs and, like caecilians, are classified as tetrapods because they are descended from four-limbed ancestors. Reptiles lay shelled eggs on land. Even aquatic reptiles, like sea turtles, return to the land to lay eggs. They usually reproduce sexually with internal fertilization. Some species display ovoviviparity, with the eggs remaining in the mother’s body until they are ready to hatch. Other species are viviparous, with the offspring born alive.

Characteristics of Reptiles

One of the key adaptations that permitted reptiles to live on land was the development of their scaly skin, containing the protein keratin and waxy lipids, which reduced water loss from the skin. A number of keratinous epidermal structures have emerged in the descendants of various reptilian lineages and some have become defining characters for these lineages: scales, claws, nails, horns, feathers, and hair. Their occlusive skin means that reptiles cannot use their skin for respiration, like amphibians, and thus all amniotes breathe with lungs. All reptiles grow throughout their lives and regularly shed their skin, both to accommodate their growth and to rid themselves of ectoparasites. Snakes tend to shed the entire skin at one time, but other reptiles shed their skins in patches.

Reptiles ventilate their lungs using various muscular mechanisms to produce negative pressure (low pressure) within the lungs that allows them to expand and draw in air. In snakes and lizards, the muscles of the spine and ribs are used to expand or contract the rib cage. Since walking or running interferes with this activity, the squamates cannot breathe effectively while running. Some squamates can supplement rib movement with buccal pumping through the nose, with the mouth closed. In crocodilians, the lung chamber is expanded and contracted by moving the liver, which is attached to the pelvis. Turtles have a special problem with breathing, because their rib cage cannot expand. However, they can change the pressure around the lungs by pulling their limbs in and out of the shell, and by moving their internal organs. Some turtles also have a posterior respiratory sac that opens off the hindgut that aids in the diffusion of gases.

Reptiles are ectotherms, that is, animals whose main source of body heat comes from the environment. Behavioral maneuvers, like basking to heat themselves, or seeking shade or burrows to cool off, help them regulate their body temperature.

Evolution of Reptiles

Reptiles originated approximately 300 million years ago during the Carboniferous period. One of the oldest known amniotes is Casineria, which had both amphibian and reptilian characteristics. One of the earliest undisputed reptile fossils was Hylonomus, a lizardlike animal about 20 cm long. Soon after the first amniotes appeared, they diverged into three groups—synapsids, anapsids, and diapsids—during the Permian period. The Permian period also saw a second major divergence of diapsid reptiles into stem archosaurs (predecessors of thecodonts, crocodilians, dinosaurs, and birds) and lepidosaurs (predecessors of snakes and lizards). These groups remained inconspicuous until the Triassic period, when the archosaurs became the dominant terrestrial group possibly due to the extinction of large-bodied anapsids and synapsids during the Permian-Triassic extinction. About 250 million years ago, archosaurs radiated into the pterosaurs and both saurischian “lizard hip” and ornithischian “bird-hip” dinosaurs (see below).

Dinosaurs (“fearfully-great lizard”) include the Saurischia (“lizard-hipped”) with a simple, three-pronged pelvis, and Ornithischia (“bird-hipped”) dinosaurs with a more complex pelvis, superficially similar to that of birds. However, it is a fact that birds evolved from the saurischian “lizard hipped” lineage, not the ornithischian “bird hip” lineage. Dinosaurs and their theropod descendants, the birds, are remnants of what was formerly a hugely diverse group of reptiles, some of which like Argentinosaurus were nearly 40 meters (130 feet) in length and weighed at least 80,000 kg (88 tons). They were the largest land animals to have lived, challenging and perhaps exceeding the great blue whale in size, but probably not weight—which could be greater than 200 tons. Both the ornithischian and saurischian dinosaurs provided parental care for their broods, just as crocodilians and birds do today. The end of the age of dinosaurs came about 65 million years ago, during the Mesozoic, coinciding with the impact of a large asteroid (that produced the Chicxulub crater) in what is now the Yucatan Peninsula of Mexico. Besides the immediate environmental disasters associated with this asteroid impacting the Earth at about 45,000 miles per hour, the impact may also have helped generate an enormous series of volcanic eruptions that changed the distribution and abundance of plant life worldwide, as well as its climate.

Although they are sometimes mistakenly called dinosaurs, the pterosaurs were distinct from true dinosaurs. Pterosaurs had a number of adaptations that allowed for flight, including hollow bones (birds also exhibit hollow bones, a case of convergent evolution). Their wings were formed by membranes of skin that attached to the long, fourth finger of each arm and extended along the body to the legs. More than 200 species of pterosaurs have been described, and in their day, beginning about 230 million years ago, they were the undisputed rulers of the Mesozoic skies for over 170 million years. Recent fossils suggest that hundreds of pterosaur species may have lived during any given period, dividing up the environment much like birds do today. Pterosaurs came in amazing sizes and shapes, ranging in size from that of a small song bird to that of the enormous Quetzalcoatlus northropi, which stood nearly 6 meters (19 feet) high and had a wingspan of nearly 14 meters (40 feet). This monstrous pterosaur, named after the Aztec god Quetzalcoatl, the feathered flying serpent that contributed largely to the creation of humankind, may have been the largest flying animal that ever evolved!

In contrast to the aerial pterosaurs, the dinosaurs were a diverse group of terrestrial reptiles with more than 1,000 species classified to date. Paleontologists continue to discover new species of dinosaurs. Some dinosaurs were quadrupeds; others were bipeds. Some were carnivorous, whereas others were herbivorous. Dinosaurs laid eggs, and a number of nests containing fossilized eggs, with intact embryos, have been found. It is not known with certainty whether dinosaurs were homeotherms or facultative endotherms. However, given that modern birds are endothermic, the dinosaurs that were the immediate ancestors to birds likely were endothermic as well. Some fossil evidence exists for dinosaurian parental care, and comparative biology supports this hypothesis since the archosaur birds and crocodilians both display extensive parental care.

Dinosaurs dominated the Mesozoic era, which was known as the “Age of Reptiles.” The dominance of dinosaurs lasted until the end of the Cretaceous, the last period of the Mesozoic era. The Cretaceous-Tertiary extinction resulted in the loss of most of the large-bodied animals of the Mesozoic era. Birds are the only living descendants of one of the major clades of theropod dinosaurs.

Diversity of Modern Reptiles

Class Reptilia includes diverse species classified into four living clades. These are the Crocodilia, Sphenodontia, Squamata, and Testudines.

The Crocodilia (“small lizard”) arose approximately 84 million years ago, and living species include alligators, crocodiles, and caimans. Crocodilians (Figure 15.59a) live throughout the tropics of Africa, South America, the southeastern United States, Asia, and Australia. They are found in freshwater habitats, such as rivers and lakes, and spend most of their time in water. Crocodiles are descended from terrestrial reptiles and can still walk and run well on land. They often move on their bellies in a swimming motion, propelled by alternate movements of their legs. However, some species can lift their bodies off the ground, pulling their legs in under the body with their feet rotated to face forward. This mode of locomotion takes a lot of energy, and seems to be used primarily to clear ground obstacles.

The Sphenodontia (“wedge tooth”) arose in the Mesozoic Era and includes only one living genus, Tuatara, with two species that are found in New Zealand. There are many fossil species extending back to the Triassic period (250–200 million years ago). Although the tuataras resemble lizards, they are anatomically distinct and share characteristics that are found in birds and turtles.

Squamata (“scaly”) arose in the late Permian; living species include lizards and snakes, which are the largest extant clade of reptiles. Both are found on all continents except Antarctica. Lizards and snakes are most closely related to tuataras, both groups having evolved from a lepidosaurian ancestor.

Most lizards differ from snakes by having four limbs, although these have often been lost or significantly reduced in at least 60 lineages. Snakes lack eyelids and external ears, which are both present in lizards. There are about 6,000 species of lizards, ranging in size from tiny chameleons and geckos, some of which are only a few centimeters in length, to the Komodo dragon, which is about 3 meters in length.

Some lizards are extravagantly decorated with spines, crests, and frills, and many are brightly colored. Some lizards, like chameleons (Figure 15.59b), can change their skin color by redistributing pigment within chromatophores in their skins. Chameleons change color both for camouflage and for social signaling. Lizards have multiple-colored oil droplets in their retinal cells that give them a good range of color vision. Lizards, unlike snakes, can focus their eyes by changing the shape of the lens. The eyes of chameleons can move independently. Several species of lizards have a “hidden” parietal eye, similar to that in the tuatara. Both lizards and snakes use their tongues to sample the environment and a pit in the roof of the mouth, Jacobson’s organ, is used to evaluate the collected sample.

Most lizards are carnivorous, but some large species, such as iguanas, are herbivores. Some predatory lizards are ambush predators, waiting quietly until their prey is close enough for a quick grab. Others are patient foragers, moving slowly through their environment to detect possible prey. Lizard tongues are long and sticky and can be extended at high speed for capturing insects or other small prey. Traditionally, the only venomous lizards are the Gila monster and the beaded lizard. However, venom glands have also been identified in several species of monitors and iguanids, but the venom is not injected directly and should probably be regarded as a toxin delivered with the bite.

Specialized features of the jaw are related to adaptations for feeding that have evolved to feed on relatively large prey (even though some current species have reversed this trend). Snakes are thought to have descended from either burrowing or aquatic lizards over 100 million years ago (Figure 15.59c). They include about 3,600 species, ranging in size from 10 centimeter-long thread snakes to 10 meter-long pythons and anacondas. All snakes are legless, except for boids (e.g., boa constrictors), which have vestigial hindlimbs in the form of pelvic spurs. Like caecilian amphibians, the narrow bodies of most snakes have only a single functional lung. All snakes are carnivorous and eat small animals, birds, eggs, fish, and insects.

Most snakes have a skull that is very flexible, involving eight rotational joints. They also differ from other squamates by having mandibles (lower jaws) without either bony or ligamentous attachment anteriorly. Having this connection via skin and muscle allows for great dynamic expansion of the gape and independent motion of the two sides—both advantages in swallowing big prey. Most snakes are nonvenomous and simply swallow their prey alive, or subdue it by constriction before swallowing it. Venomous snakes use their venom both to kill or immobilize their prey, and to help digest it.

Although snakes have no eyelids, their eyes are protected with a transparent scale. Their retinas have both rods and cones, and like many animals, they do not have receptor pigments for red light. Some species, however, can see in the ultraviolet, which allows them to track ultraviolet signals in rodent trails. Snakes adjust focus by moving their heads. They have lost both external and middle ears, although their inner ears are sensitive to ground vibrations. Snakes have a number of sensory structures that assist in tracking prey. In pit vipers, like rattlesnakes, a sensory pit between the eye and nostrils is sensitive to infrared (“heat”) emissions from warm-blooded prey. A row of similar pits is located on the upper lip of boids. As noted above, snakes also use Jacobson’s organ for detecting olfactory signals.

Turtles are members of the clade Testudines (“having a shell”) (Figure 15.59d). Turtles are characterized by a bony or cartilaginous shell, made up of the carapace on the back and the plastron on the ventral surface, which develops from the ribs. Turtles arose approximately 200 million years ago, predating crocodiles, lizards, and snakes. Turtles lay eggs on land, although many species live in or near water. Turtles range in size from the speckled padloper tortoise at 8 centimeters (3.1 inches) to the leatherback sea turtle at 200 centimeters (over 6 feet). The term “turtle” is sometimes used to describe only those species of Testudines that live in the sea, with the terms “tortoise” and “terrapin” used to refer to species that live on land and in fresh water, respectively.

Birds

With over 10,000 identified species, the birds are the most speciose of the land vertebrate classes. Abundant research has shown that birds are really an extant clade that evolved from maniraptoran theropod dinosaurs about 150 million years ago. Thus, even though the most obvious characteristic that seems to set birds apart from other extant vertebrates is the presence of feathers, we now know that feathers probably appeared in the common ancestor of both ornithischian and saurischian lineages of dinosaurs. Feathers in these clades are also homologous to reptilian scales and mammalian hair, according to the most recent research. While the wings of vertebrates like bats function without feathers, birds rely on feathers, and wings, along with other modifications of body structure and physiology, for flight, as we shall see.

Characteristics of Birds

Birds are endothermic, and more specifically, homeothermic—meaning that they usually maintain an elevated and constant body temperature, which is significantly above the average body temperature of most mammals. This is, in part, due to the fact that active flight—especially the hovering skills of birds such as hummingbirds—requires enormous amounts of energy, which in turn necessitates a high metabolic rate. Like mammals (which are also endothermic and homeothermic and covered with an insulating pelage), birds have several different types of feathers that together keep “heat” (infrared energy) within the core of the body, away from the surface where it can be lost by radiation and convection to the environment.

Modern birds produce two main types of feathers: contour feathers and down feathers. Contour feathers have a number of parallel barbs that branch from a central shaft. The barbs in turn have microscopic branches called barbules that are linked together by minute hooks, making the vane of a feather a strong, flexible, and uninterrupted surface. In contrast, the barbules of down feathers do not interlock, making these feathers especially good for insulation, trapping air in spaces between the loose, interlocking barbules of adjacent feathers to decrease the rate of heat loss by convection and radiation. Certain parts of a bird’s body are covered in down feathers, and the base of other feathers has a downy portion, whereas newly hatched birds are covered almost entirely in down, which serves as an excellent coat of insulation, increasing the thermal boundary layer between the skin and the outside environment.

Feathers not only provide insulation, but also allow for flight, producing the lift and thrust necessary for flying birds to become and stay airborne. The feathers on a wing are flexible, so the feathers at the end of the wing separate as air moves over them, reducing the drag on the wing. Flight feathers are also asymmetrical and curved, so that air flowing over them generates lift. Two types of flight feathers are found on the wings, primary feathers and secondary feathers (Figure 15.60). Primary feathers are located at the tip of the wing and provide thrust as the bird moves its wings downward, using the pectoralis major muscles. Secondary feathers are located closer to the body, in the forearm portion of the wing, and provide lift. In contrast to primary and secondary feathers, contour feathers are found on the body, where they help reduce form drag produced by wind resistance against the body during flight. They create a smooth, aerodynamic surface so that air moves swiftly over the bird’s body, preventing turbulence and creating ideal aerodynamic conditions for efficient flight.

Feathers not only permitted the earliest birds to glide, and ultimately engage in flapping flight, but they insulated the bird’s body, assisting the maintenance of endothermy, even in cooler temperatures. Powering a flying animal requires economizing on the amount of weight carried. As body weight increases, the muscle output and energetic cost required for flying increase. Birds have made several modifications to reduce body weight, including hollow or pneumatic bones (Figure 15.60b) with air spaces that may be connected to air sacs and cross-linked struts within their bones to provide structural reinforcement. Parts of the vertebral skeleton and braincase are fused to increase its strength while lightening its weight. Most species of bird only possess one ovary rather than two, and no living birds have teeth in their jaw, further reducing body mass.

Birds possess a system of air sacs branching from their primary airway that divert the path of air so that it passes unidirectionally through the lung, during both inspiration and expiration. Unlike mammalian lungs in which air flows in two directions as it is breathed in and out, air flows continuously through the bird’s lung to provide a more efficient system of gas exchange.

All these unique and highly derived characteristics make birds one of the most conspicuous and successful groups of vertebrate animals, filling a range of ecological niches, and ranging in size from the tiny bee hummingbird of Cuba (about 2 grams) to the ostrich (about 140,000 grams). Their large brains, keen senses, and the abilities of many species to imitate vocalization and use tools make them some of the most intelligent vertebrates on Earth.