Lungs of the first amniotes: why simple if they can be complex?
Authors:
Lambertz et al
Abstract:
We show—in contrast to the traditional textbook contention—that the first amniote lungs were complex, multichambered organs and that the single-chambered lungs of lizards and snakes represent a secondarily simplified rather than the plesiomorphic condition. We combine comparative anatomical and embryological data and show that shared structural principles of multichamberedness are recognizable in amniotes including all lepidosaurian taxa. Sequential intrapulmonary branching observed during early organogenesis becomes obscured during subsequent growth, resulting in a secondarily simplified, functionally single-chambered lung in lepidosaurian adults. Simplification of pulmonary structure maximized the size of the smallest air spaces and eliminated biophysically compelling surface tension problems that were associated with miniaturization evident among stem lepidosaurmorphs. The remaining amniotes, however, retained the multichambered lungs, which allowed both large surface area and high pulmonary compliance, thus initially providing a strong selective advantage for efficient respiration in terrestrial environments. Branched, multichambered lungs instead of simple, sac-like organs were part and parcel of the respiratory apparatus of the first amniotes and pivotal for their success on dry land, with the sky literally as the limit.
Showing posts with label lungs. Show all posts
Showing posts with label lungs. Show all posts
Wednesday, January 28, 2015
Were Amniote Lungs Basally Complex?
Labels:
amniotes,
embryos,
evolution,
lungs,
paleobiology
Tuesday, November 18, 2014
Unidirectional Lungs Basal to Diapsids: Green Iguanas Breathe Like Birds
Whether birds are breathing in or out, air flows in a one-directional loop through their lungs. This pattern was unexpected and for decades, biologists assumed it was unique to birds, a special adaptation driven by the intense energy demands of flight.
But that view is wrong, according to University of Utah scientists who now have shown that bird-like breathing also developed in green iguanas - reptiles not known for high-capacity aerobic fitness. The finding bolsters the case that unidirectional bird-like flow evolved long before the first birds, arising nearly 300 million years ago in a common ancestor of lizards, snakes, crocodiles and dinosaurs including birds.
"We thought we understood how these lungs work, but in fact most of us were completely wrong," says Colleen Farmer, an associate professor of biology at the U and lead author of the new study published today in Proceedings of the National Academy of Sciences. "People have made a lot of assumptions about how lungs work in animals such as reptiles and crocodiles but they never actually measured flow," she says.
In humans and other mammals, lungs have airways with a tree-like branching structure. A main trunk in each lung splits into branches and twigs. Air flows in and out in a tidal fashion. Oxygen and carbon dioxide pass to and from blood in tiny air sacs, called alveoli, at the tips of the smallest airway branches.
In bird lungs, air loops in one direction through a series of tubes lined with blood vessels for gas exchange. Aerodynamic forces act like valves to sustain the one-way flow through cycles of inhalation and exhalation.
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