Coelacanths are lobe-finned fishes known from the Devonian to Recent that were long considered extinct, until the discovery of two living species in deep marine waters of the Mozambique Channel and Sulawesi. Despite extensive studies, the pulmonary system of extant coelacanths has not been fully investigated. Here we confirm the presence of a lung and discuss its allometric growth in Latimeria chalumnae, based on a unique ontogenetic series. Our results demonstrate the presence of a potentially functional, well-developed lung in the earliest known coelacanth embryo, and its arrested growth at later ontogenetic stages, when the lung is clearly vestigial. The parallel development of a fatty organ for buoyancy control suggests a unique adaptation to deep-water environments. Furthermore, we provide the first evidence for the presence of small, hard, flexible plates around the lung in L. chalumnae, and consider them homologous to the plates of the ‘calcified lung’ of fossil coelacanths.
Coelacanths form a clade of predatory sarcopterygian fishes known from the early Devonian (−410 Myr) to Recent, with the iconic species Latimeria chalumnae1 and L. menadoensis2,3. Fossil coelacanths are morphologically and taxonomically diverse (with more than 130 species), and globally distributed in various aquatic environments (fresh, brackish to marine waters)4. The evolutionary history of coelacanths is long and complex, and the living coelacanths cannot be considered as living fossils. There is a large gap of ∼70 Myr between the extant Latimeria and the youngest fossil coelacanth remains, Megalocoelacanthus dobei and an isolated angular of a mawsoniid coelacanth, both from the Upper Cretaceous5,6,7. This absence from the Cenozoic fossil record caused this group to be long considered as extinct since the Cretaceous/Palaeogene (K/Pg) environmental crisis. The discovery in 1938 of the extant species L. chalumnae offshore South Africa in the Indian Ocean1 was followed by numerous articles on the anatomy, physiology and phylogeny of this group, turning it into either an iconic ‘living fossil’ or a ‘Lazarus taxon’; that is, a born-again member of a reputedly extinct group1,4,8,9,10,11.
Latimeria is a heavily built fish living in rocky environments between 110 and 400 m deep in the coastal waters of the Mozambique Channel and of Sulawesi12,13,14. This large animal (up to 2 m long) is ovoviviparous15. The young develop in the oviduct of the female, which can give birth to 26 live pups of about 35 cm long16. Juvenile coelacanths (below 80 cm long) are rarely observed or caught17.
The presence of a large calcified sheath in the abdominal cavity of fossil coelacanths has been known since the 19th century18,19 but was previously regarded as either an ‘internal osseous viscus’ (unknown internal organ), a bladder or swimbladder. Only recently this organ has been formally described in Palaeozoic and Mesozoic coelacanths as a pulmonary organ composed of large and rounded calcified plates, positioned ventrally relative to the gut, and with a single anterior opening under the opercle20.
Although the anatomy of living coelacanth has been extensively studied, little is known about its lung. L. chalumnae does not possess a calcified organ in its abdominal cavity, but a short oesophageal diverticulum surrounded by a fatty organ. Many aspects of the anatomy and the development of these structures in Latimeria remain unclear, as well as their homology to the calcified organ of many fossil coelacanths.
Here we confirm the presence of a lung in L. chalumnae and present its allometric growth based on a unique ontogenetic series. We also propose the first evidence of the homology between this lung and the ‘calcified lung’ of fossil coelacanths, based on the presence of small plates around the lung in the extant species. The parallel development of a fatty organ for buoyancy control suggests a unique adaptation to deep water.
The lung of Latimeria
The pulmonary complex of L. chalumnae comprises a vestigial lung (oesophageal diverticulum) derived from the ventral portion of the oesophagus (Fig. 1). The presence of an oesophageal diverticulum in a medio-ventral position relative to the oesophagus, its non-obliterated opening (Fig. 2a), its internal cavity (Fig. 2b), as well as invaginations in the anterior part of its internal wall (Fig. 2b,c) characterizes this structure as a lung.
The vestigial lung of L. chalumnae is included in the anteriormost part of a large, closed and tubular sheath filled with fat (Fig. 1). This so-called ‘fatty organ’10,20, previously referred in the literature as a swimbladder21, air bladder4, fatty lung20 and modified lung or bladder22, has a ventral position relative to the oesophagus, turns dorsally relative to the stomach and reaches the posterior wall of the abdominal cavity10. This organ in Latimeria is structurally different from the swimbladder of many actinopterygians that is, in the latter group, an air sac with, or without, an anterior opening located on the dorsal side of the oesophagus.
Dissections, three-dimensional reconstructions and histological analyses have revealed small, hard, but flexible plates scattered around the vestigial lung in adult specimens but not around the fatty organ (Fig. 3a–e). These plates correspond to the misinterpreted ‘artères involuées’10, and are quite similar in shape and position to the bony plates found in many fossil coelacanth taxa20.
The lung development in Latimeria
There is a marked allometric growth of the lung compared with the growth of the fatty organ (Fig. 1). While the fatty organ’s proportions relative to the total length (TL) increase proportionally according to the ontogenetic stages of individuals, the relative proportions between the lung and the TL of the specimens decrease in the juvenile (Supplementary Fig. 1) before stabilizing in the adult stage (Fig. 1i–l).
Moreover, the ratio between lung’s length and the fatty organ’s length is much higher in embryos (Fig. 1a–h) than in the juvenile (Supplementary Fig. 1) and adult (Fig. 1i–l) specimens. In the earliest embryo CCC 202.1 (4 cm TL), the lung’s length corresponds to more than half of the length of the fatty organ, whereas this ratio decreases considerably in the juvenile specimen (Supplementary Fig. 1).
The oesophageal diverticulum of the earliest embryo is inflated throughout its length, which likely foreshadows a normal developmental stage towards a functional organ (Fig. 1d). In the following successive ontogenetic stages (CCC 29.5, CCC 162.21) the oesophageal diverticulum is markedly reduced to become a very thin and long filament here called the ‘residual filament’, the inflated part being restricted to the anteriormost region (Fig. 1h; Supplementary Fig. 2).
Our discovery of hard but flexible plates around the vestigial lung (oesophageal diverticulum) of adult specimens of L. chalumnae documents the first evidence of the homology between its lung and the long debated ‘calcified lung’ of fossil coelacanths (Supplementary Figs 3 and 4), questioning previous hypothesis of the fatty organ as part of the pulmonary complex10. In the Cretaceous coelacanth Axelrodichthys, the ossified plates surrounding the lung most probably had a function in lung volume regulation, with the plates moving over each other to accommodate volumetric changes20, while in L. chalumnae these plates are a rudimentary anatomical structure.
Here we demonstrate also the presence of a well-developed, potentially functional, lung in the earliest known L. chalumnae embryo, suggesting the presence of a functional lung in early fossil coelacanths. These animals lived in shallow brackish, fresh or marine environments and, like in some extant lungfishes and polypteriforms, air breathing might have been an essential respiratory need. The presence of a lung in Latimeria confirms that this organ is a general character for all osteichthyans, as it is also present in basal actinopterygians, lungfishes and tetrapods, notably land vertebrates23,24.
The extant coelacanth L. chalumnae has no functional air-breathing organ10, and the main oxygen supply is provided through the gills25. However, the low surface area of the Latimeria gills and the thick tissue barrier separating water from blood in the gill filaments26 could be evidence for a low branchial oxygen intake capacity in fossil coelacanths, which required a supplementary air-breathing supply, especially in shallow-water hypoxic conditions. In the Mesozoic Era, adaptation of some coelacanths to deep marine water, an environment with very low variations of oxygen pressure, may have triggered the total loss of pulmonary respiration, the marked reduction of the lung and the increase of the fatty organ as a buoyancy adaptation to deeper environments.
This adaptation to deep water may help explain the survival of some coelacanths throughout the Cretaceous/Palaeogene (K/Pg) environmental crisis, whereas Late Cretaceous coelacanths inhabiting shallow waters disappeared. Therefore, the apparent absence of coelacanths in the fossil record since the end of the Mesozoic is merely due to a lack of Cenozoic fossil coelacanths so far, and scarce preservation of Cenozoic deep-water sediments. Although we cannot know whether the fatty organ ever existed in fossil forms, due to its unique soft-tissue constitution, this organ in Latimeria has a function in buoyancy control. Such an organ seems to be functionally analogous to the liver of sharks27,28, the fat-invested string of tissue of some deep-water ray-finned fishes29 or the spermaceti of some cetaceans30,31.
The five different ontogenetic stages of L. chalumnae imaged using X-ray tomography come from Tanzania, Comoro Islands and Mozambique: CCC 202.1 (SAIAB 76199) is an early embryo of 4 cm TL, discovered inside the female CCC 202 fished in Tanzania in 2005. CCC 29.5 (MNHN 26.5) is a late embryo with a yolk sac, 32.3 cm TL, discovered inside the female CCC 29, fished in Comoro Islands in 1962. CCC 162.21 (ZSM 28409) is a late embryo without a yolk sac, 35.6 cm TL, discovered inside the female CCC 126 fished in Mozambique in 1991. CCC 94 (MNHN C79) is a young female, 42.5 cm TL, fished in Comoro Islands in 1974. The adult specimens are the following: CCC 22 (MNHN C20), male, 130 cm TL, Comoro Islands, 1960. CCC 28 (MNHN C25), male, 130 cm TL, Comoro Islands, 1962 (isolated viscus). Direct anatomical observations were made from new dissections of specimens CCC 28 and CCC 3 (MNHN C3, isolated viscus from an adult male of 129 cm TL, fished in Comoro Islands in 1953). Histological observations were made from unpublished thin sections prepared from specimen CCC 5 (MNHN C5, adult male of 127 cm TL, Comoro Islands, 1954) by Millot, Anthony and Robineau. More details on the information inventory of these specimens are provided elsewhere17,32. The histological material is deposited in the Collection of Comparative Anatomy of the Muséum national d’Histoire naturelle (France). The fossil adult specimen of Macropoma mantelli Agassiz, 1843 NHMUK PV P 2051, was recovered from Cretaceous Chalk Formation, Sussex (England).
Institutional abbreviations: SAIAB, South African Institute for Aquatic Biodiversity, Grahamstown (South Africa); MNHN, Muséum national d’Histoire naturelle; ZSM, Zoologische Staatssammlung, München (Germany); NHMUK, Natural History Museum United Kingdom, London (UK). CCC, Coelacanth Conservation Council.
The specimens CCC 202.1, CCC 29.5, CCC 162.21 and CCC 94 were scanned using long propagation phase-contrast synchrotron X-ray microtomography at the ID19 beamline of the European Synchrotron Radiation Facility, Grenoble (France). CCC 202.1 was imaged supported in a glass cylinder vase filled with ethanol (resulting in a negative contrast agent effect), voxel size 6.5 μm, with a high-quality pink beam using the ID19 W150 wiggler at a gap of 50 mm filtered by 2 mm of aluminium, 0.25 mm of copper and 0.2 mm of gold. The scintillator was a 250-μm-thick LuAG:Ce (lutetium–aluminium–garnet) crystal. The resulting detected spectrum was then centred on 77 keV, with a bandwidth of 17 keV FWHM (full width at half maximum). The detector was a FreLoN 2K charge coupled device (CCD) camera33 mounted on a lens system. To obtain a sufficient propagation phase-contrast effect, a distance of 3 m between the sample and the detector was used. The final reconstruction (13 μm) was obtained after binning. CCC 162.21 was scanned in a plastic tube filled with water, voxel size 30.45 μm, using the ID19 W150 wiggler at a gap of 50 mm filtered by 2 mm of aluminium, 0.25 mm of copper and 0.25 mm of tungsten. The scintillator, detector and distance between the sample and the detector were the same as for CCC 202.1. The final reconstruction (60.90 μm) was obtained after binning. Specimens CCC 29.5 and CCC 94 were scanned in a plastic tube filled with water, voxel size 28.43 μm, using a propagation distance of 13 m to maximize the phase-contrast effect. For CCC 94, the beam produced by the wiggler at a gap of 30 mm was filtered by 2 mm of aluminium and 15 mm of copper, resulting in an average detected energy of 170 keV with a bandwidth of 85 keV FWHM. For CCC 29.5, a lower energy was used: wiggler at a gap of 45 mm filtered by 2 mm of aluminium and 6 mm of copper. The resulting spectrum had an average detected energy of 120 keV with a bandwidth of 57 keV FWHM. For both specimens the detector camera was a FreLoN 2K charge coupled device33 mounted on a lens system composed of a 750-μm-thick LuAG:Ce scintillator. The final reconstructions (113.72 μm for CCC 29.5 and 85.29 μm for CCC 94) were obtained after binning. In all cases, the slices were reconstructed using a filtered back-projection algorithm coupled with a single distance phase-retrieval process34,35. For each sample, all the sub-scans were reconstructed separately, converted into 16-bit TIFF stacks and then concatenated to generate a single complete scan of each specimen. The ring artefacts were corrected on the reconstructed slices using a specific tool developed at the European Synchrotron Radiation Facility36. A high-resolution computerized axial tomography scanning (CAT scan) was performed for the specimen CCC 22 in a Parisian Hospital (France) using the following scanning parameters: effective energy 120 kV, current 158 mA, voxel size 742 μm and 1,807 views. For the specimen CCC 28, a CAT scan was acquired at the Platform AST-RX of the Muséum national d’Histoire naturelle, using an effective energy of 245 kV, current 430 mA, voxel size 54.24 μm, and 2,550 views. Images were reconstructed and exported into 16-bit TIFF stacks using the phoenix datos|x 2.0 reconstruction software, and exported into 16-bit TIFF stacks. For all the specimens, segmentation and three-dimensional rendering were realized at the Palaeontology Imaging Unit of the MNHN Département Histoire de la Terre/UMR 7207 CR2P CNRS/MNHN/UPMC using the software MIMICS Innovation Suite 16.0 (Materialise).
How to cite this article: Cupello, C. et al. Allometric growth in the extant coelacanth lung during ontogenetic development. Nat. Commun. 6:8222 doi: 10.1038/ncomms9222 (2015).
Smith, J. L. B. A living fish of Mesozoic type. Nature 143, 455–456 (1939).
Erdmann, M. V., Caldwell, R. L. & Kasim Moosa, M. Indonesian ‘king of the sea’ discovered. Nature 395, 335 (1998).
Pouyaud, L. et al. Une nouvelle espèce de coelacanthe: preuves génétiques et morphologiques. CR. Acad. Sci. III-VIE 322, 261–267 (1999).
Forey, P. L. History of the Coelacanth Fishes Chapman and Hall (1998).
Schwimmer, D. R., Stewart, J. D. & Williams, G. D. Giant fossil coelacanths of the Late Cretaceous in the eastern United States. Geology 22, 503–506 (1994).
Cavin, L., Forey, P. L., Buffetaut, E. & Tong, H. Latest European coelacanth shows Gondwanan affinities. Biol. Lett. 1, 176–177 (2005).
Dutel, H. et al. The giant Cretaceous coelacanth (Actinistia, Sarcopterygii) Megalocoelacanthus dobiei Schwimmer, Stewart & Williams, 1994, and its bearing on Latimerioidei interrelationships. PLoS ONE 7, e49911 (2012).
Millot, J. & Anthony, J. Anatomie de Latimeria chalumnae I CNRS (1958).
Millot, J. & Anthony, J. Anatomie de Latimeria chalumnae II CNRS (1965).
Millot, J., Anthony, J. & Robineau, D. Anatomie de Latimeria chalumnae III CNRS (1978).
Amemiya, C. T. et al. The African coelacanth genome provides insights into tetrapod evolution. Nature 496, 311–316 (2013).
Fricke, H. et al. Habitat and population size of the coelacanth Latimeria chalumnae at Grand Comoro. Environ. Biol. Fish. 32, 287–300 (1991).
Fricke, H. et al. Biogeography of the Indonesian coelacanths. Nature 403, 38 (2000).
Hissmann, K. et al. The South African coelacanths– an account of what is known after three submersible expeditions. S. Afr. J. Sci. 102, 491–500 (2006).
Smith, C. L., Rand, C. S., Schaeffer, B. & Atz, J. W. Latimeria, the living coelacanth, is ovoviviparous. Science 190, 1105–1106 (1975).
Bruton, M. N., Cabral, A. J. P. & Fricke, H. First capture of a coelacanth, Latimeria chalumnae (Pisces, Latimeriidae), off Mozambique. S. Afr. J. Sci. 88, 225–227 (1992).
Nulens, R., Scott, L. & Herbin, M. An Updated Inventory of all Known Specimens of the Coelacanth Latimeria spp. South African Institute for Aquatic Biodiversity3, 1–52 (2011).
Williamson, W. C. On the microscopic structure of the scales and dermal teeth of some ganoid and placoid fish. Philos. Trans. R. Soc. Lond. 139, 435–475 (1849).
Woodward, A. S. Catalogue of Fossil Fishes in the British Museum (Natural History) British Museum (Natural History) (1891).
Brito, P. M., Meunier, F. J., Clément, G. & Geffard-Kuriyama, D. The histological structure of the calcified lung of the fossil coelacanth Axelrodichthys araripensis (Actinistia: Mawsoniidae). Palaeontology 53, 1281–1290 (2010).
Cloutier, R. Patterns, trends, and rates of evolution within the Actinistia. Environ. Biol. Fish. 32, 23–58 (1991).
Forey, P. Coelacanth: Portrait of a Living Fossil Forrest Text (2009).
Janvier, P. Early Vertebrates Oxford Univ. Press (1996).
Longo, S., Riccio, M. & McCune, A. R. Homology of lungs and gas bladders: insights from arterial vasculature. J. Morphol. 274, 687–703 (2013).
Millot, J. Le Troisième Coelacanthe Le Naturaliste Malgache. Premier Supplément (1954).
Hughes, G. M. The gills of the coelacanth Latimeria chalumnae Latimeriidae. What can they teach us? Ital. J. Zool. 65, 425–429 (1998).
Corner, E. D. S., Denton, E. J. & Forster, G. R. On the buoyancy of some deep-sea sharks. Proc. R. Soc. Lond. B Biol. Sci. 171, 415–429 (1969).
Helfman, G. S., Collette, B. B. & Facey, D. E. in The Diversity of Fishes eds Helfman G. S., Collette B. B., Facey D. E. 205–230Wiley-Blackwell (1997).
Norman, J. R. A History of Fishes Ernest Benn Ltd. (1975).
Ridgway, S. H. Buoyancy regulation in deep diving whales. Nature 232, 133–134 (1971).
Clarke, M. R. Buoyancy control as a function of the spermaceti organ in the sperm whale. J. Mar. Biol. Assoc. UK 58, 27–71 (1978).
Bruton, M. N. & Coutouvidis, S. E. An inventory of all known specimens of the coelacanth Latimeria chalumnae, with comments on trends in the catches. Environ. Biol. Fish. 32, 371–390 (1991).
Labiche, J.-C. et al. The fast readout low noise camera as a versatile X-ray detector for time resolved dispersive extended X-ray absorption fine structure and diffraction studies of dynamic problems in materials science, chemistry, and catalysis. Rev. Sci. Instrum. 78, 091301 (2007).
Paganin, D., Mayo, S. C., Gureyev, T. E., Miller, P. R. & Wilkins, S. W. Simultaneous phase and amplitude extraction from a single defocused image of a homogeneous object. J. Microsc. 206, 33–40 (2002).
Sanchez, S., Ahlberg, P. E., Trinajstic, K., Mirone, A. & Tafforeau, P. Three dimensional synchrotron virtual paleohistology: a new insight into the world of fossil bone microstructures. Microsc. Microanal. 18, 1095–1105 (2012).
Lyckegaard, A., Johnson, G. & Tafforeau, P. Correction of ring artifacts in X-ray tomographic images. Int. J. Tomo. Stat. 18, 1–9 (2011).
The synchrotron experiments were performed on the ID19 beamline at the European Synchrotron Radiation Facility (ESRF), Grenoble, France. We are grateful to P. Tafforeau at ESRF for providing assistance in using beamline ID19. We thank M. García Sanz at the X-ray Tomography Imagery Platform AST-RX of the UMS2700, MNHN, Paris, France (funded by MNHN, CNRS, Institut de France, Région Ile-de-France) for the X-ray tomography scans and F. Goussard (UMR 7207 CR2P CNRS–MNHN-UPMC-Paris6) for providing 3D imaging facilities. Thanks to P. Loubry and L. Cazes (UMR CR2P MNHN/CNRS/UPMC) for the photographs of specimens CCC 29.5 and CCC 94. We warmly thank R. Bills and A. Paterson (SAIAB, Grahamstown, South Africa), D. Neumann (München, Germany) and M. Richter (London, UK) for the loans of the valuable specimens SAIAB 76199, ZSM 28409 and NHMUK PV P 2051, respectively. This research has been partially supported by the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES/Ciência sem Fronteiras), Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro and the UMR 7207 CR2P (MNHN/CNRS/UPMC). This paper is a contribution to the ANR TERRES 2010-BLAN-607-03 project.
The authors declare no competing financial interests.
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Cupello, C., Brito, P., Herbin, M. et al. Allometric growth in the extant coelacanth lung during ontogenetic development. Nat Commun 6, 8222 (2015). https://doi.org/10.1038/ncomms9222
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