Modern birds have markedly foreshortened tails and their body mass is centred anteriorly, near the wings. To provide stability during powered flight, the avian centre of mass is far from the pelvis, which poses potential balance problems for cursorial birds. To compensate, avians adapted to running maintain the femur subhorizontally, with its distal end situated anteriorly, close to the animal's centre of mass; stride generation stems largely from parasagittal rotation of the lower leg about the knee joint. In contrast, bipedal dinosaurs had a centre of mass near the hip joint and rotated the entire hindlimb during stride generation. Here we show that these contrasting styles of cursoriality are tightly linked to longer relative total hindlimb length in cursorial birds than in bipedal dinosaurs. Surprisingly, Caudipteryx, described as a theropod dinosaur, possessed an anterior centre of mass and hindlimb proportions resembling those of cursorial birds. Accordingly, Caudipteryx probably used a running mechanism more similar to that of modern cursorial birds than to that of all other bipedal dinosaurs. These observations provide valuable clues about cursoriality in Caudipteryx, but may also have implications for interpreting the locomotory status of its ancestors.

Analysis of the nasal region in fossils of three theropod dinosaurs ( Nanotyrannus, Ornithomimus, and Dromaeosaurus ) and one ornithischian dinosaur ( Hypacrosaurus ) showed that their metabolic rates were significantly lower than metabolic rates in modern birds and mammals. In extant endotherms and ectotherms, the cross-sectional area of the nasal passage scales approximately with increasing body mass M at M 0.72 . However, the cross-sectional area of nasal passages in endotherms is approximately four times that of ectotherms. The dinosaurs studied here have narrow nasal passages that are consistent with low lung ventilation rates and the absence of respiratory turbinates.

Reptiles and birds possess septate lungs rather than the alveolar-style lungs of mammals. The morphology of the unmodified, bellowslike septate lung restricts the maximum rates of respiratory gas exchange. Among taxa possessing septate lungs, only the modified avian flow-through lung is capable of the oxygen–carbon dioxide exchange rates that are typical of active endotherms. Paleontological and neontological evidence indicates that theropod dinosaurs possessed unmodified, bellowslike septate lungs that were ventilated with a crocodilelike hepatic-piston diaphragm. The earliest birds ( Archaeopteryx and enantiornithines) also possessed unmodified septate lungs but lacked a hepatic-piston diaphragm mechanism. These data are consistent with an ectothermic status for theropod dinosaurs and early birds.