LAUSR

The coelacanth, Latimeria chalumnae Smith, 1939 [1] (Sarcopterygii: Actinistia), together with the closely related L. menadoensis Pouyaud et al ., 1999 [2], remains the only living representative of one of the most basally-branching primary radiations of lobe-finned fishes (Sarcopterygii). Even though extant species cannot be considered ‘primitive’ due to the inherent logic of phylogenetic theory, the coelacanth nonetheless is invaluable for understanding evolutionary transformations in basal sarcopterygians as it can help in the determination of character polarity. The appearance of one novelty during early vertebrate evolution that had major implications for the success of a huge number of species is the origin of lungs. The conventional interpretation is that lungs evolved in basal bony fishes (Osteichthyes or Osteognathostomata), were maintained in the lobe-finned fishes, and eventually were transformed into a swimbladder among the ray-finned fishes (Actinopterygii) (e.g. [3]). However, the currently available data do not rule out separate origins of lungs and swimbladders from a common ‘respiratory pharynx’, even though this would require a slightly less parsimonious course of evolution [4,5]. The coelacanth is a key species in addressing this question and for this reason the data recently provided by Cupello and colleagues [6] are a very welcome addition to the discussion. Here, I would like to add a few points pertinent to lung evolution that appear to be a consequence of these exciting data. One of the most interesting aspects of the coelacanth is that it apparently exhibits an unpaired structure of putative homology with lungs [6–8]. In the Polypteriformes (bichir and reed fish), the lungs are paired [5,9,10], as are those of the lungfishes (Dipnoi) [11], except the Australian lungfish, Neoceratodus forsteri (Krefft, 1870) …