M Lionel Cavin

Since the discovery of Latimeria chalumnae, coelacanths have provided a critical comparative framework for reconstructing ancestral sarcopterygian anatomy. However, the function of several anatomical features in both extant and fossil coelacanths remains unresolved. Among these, the presence of large ossified chambers in the body cavity of fossil coelacanths has remained enigmatic, with different studies proposing respiratory or auditory functions. Here, we examine lung and inner ear anatomy based on new observations from synchrotron phase-contrast microCT scans of two 240-million-year-old latimerioid coelacanths, alongside multiple developmental stages of the extant L. chalumnae. These data, combined with archival histological sections of L. chalumnae and 3D reconstructions of a Devonian coelacanth, suggest that extinct coelacanths possessed an ossified lung capable of transmitting sound pressure to auditory sensory epithelia in the inner ear via a perilymphatic system. We propose that the lung of extinct coelacanths supported both respiratory and auditory functions.

This study conducted a spatiotemporal review of the coelacanth fossil record and explored its distribution and diversity patterns. Coelacanth research can be divided into two distinct periods: the first period, which is based solely on the fossil record, and the second period following the discovery of extant taxa, significantly stimulating research interest. The distribution and research intensity of coelacanth fossils exhibit marked spatial heterogeneity, with Europe and North America being the most extensively studied regions. In contrast, Asia, South America, and Oceania offer substantial potential for future research. Temporally, the coelacanth fossil record also demonstrates significant variation across geological periods, revealing three diversity peaks in the Middle Devonian, Early Triassic, and Late Jurassic, with the Early Triassic peak exhibiting the highest diversity. With the exception of the Late Devonian, Carboniferous, and Late Cretaceous, most periods remain understudied, particularly the Permian, Early Jurassic, and Middle Jurassic, where the record is notably scarce. Integrating the fossil record with phylogenetic analyses enables more robust estimations of coelacanth diversity patterns through deep time. The diversity peak observed in the Middle Devonian is consistent with early burst models of diversification, whereas the Early and Middle Triassic peaks are considered robust, and the Late Jurassic peak may be influenced by taphonomic biases. The low population abundance and limited diversity of coelacanths reduce the number of specimens available for fossilization. The absence of a Cenozoic coelacanth fossil record may be linked to their moderately deep-sea habitat. Future research should prioritize addressing gaps in the fossil record, particularly in Africa, Asia, and Latin America; employing multiple metrics to mitigate sampling biases; and integrating a broader range of taxa into phylogenetic analyses. In contrast to the widespread distribution of the fossil record, extant coelacanths exhibit a restricted distribution, underscoring the urgent need to increase conservation efforts.

The discovery in 1938 of a living coelacanth, Latimeria chalumnae, triggered much research and discussion on the evolutionary history and phylogeny of these peculiar sarcopterygian fishes. Indeed, coelacanths were thought to represent the 'missing link' between fishes and tetrapods, a phylogenetic position which is now dismissed. Since the first analyses using a phylogenetic approach were carried out three decades ago, a relatively similar data matrix has been consistently used by researchers for running analyses, with no significant changes aside from the addition of new taxa and characters, and minor corrections to the states' definition and scorings. Here, we investigate the phylogeny of Actinistia with an updated data matrix based on a list of partially new or modified characters. From the initial list of characters available in the most recent studies, we removed 16 characters, modified 16 other characters' definition and added 18 new characters, resulting in a list of 112 characters. We also revised the data matrix by correcting 171 miscoding found for 37 taxa. Based on the new phylogeny, we propose a new classification of coelacanths including 46 coelacanth genera, part of them allocated within nine families and four sub-families. Most of these groups were already named but were not recognised as clades, or poorly or not diagnosed in previous phylogenetic analyses. We provide several new or emended diagnoses for each clade. For the first time, a set of Palaeozoic coelacanth genera are found gathered within a clade, namely the Diplocercidae. All Mesozoic coelacanths, including extant Latimeria, are resolved as members of the order Coelacanthiformes, a clade that arose in the Permian, with Coelacanthus diverging first. We also found that most Mesozoic coelacanths are gathered into a clade, the Latimerioidei, itself divided into the Latimeriidae and the Mawsoniidae, each of which is divided into two subfamilies. Although these important changes, the new phylogeny of the Actinistia shows no significant alteration, and it remains relatively similar compared to previous studies. This demonstrates that the coelacanth phylogeny is now rather stable despite the weak support for most nodes in the phylogeny, and despite the difficulty of defining relevant morphological characters to score in this relatively slowly evolving lineage.

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Libanissus bkassinensis Azar, Maksoud & Nel, gen. et sp. nov. is illustrated and described from the Lower Cretaceous dysodile (oil papershales) of Bkassine, South Lebanon, and its taxonomic position discussed. Libanissus bkassinensis Azar, Maksoud & Nel, gen. et sp. nov. is characterized by its banded legs and body, a hind wing with two lobes, RA and RP very short, M with only two very short apical branches, CuA with two branches, and a small but distinct apical furcation of PCu close to the incision of the wing margin. Libanissus bkassinensis Azar, Maksoud & Nel, gen. et sp. nov. represents the earliest record (lower Barremian) of the Issidae. Prior to this discovery, the oldest known record was from the Paleocene of France.

Although the split of coelacanths from other sarcopterygians is ancient, around 420 million years ago, the taxic diversity and the morphological disparity of the clade have remained relatively low, with a few exceptions. This supposedly slow evolutionary pace has earned the extant coelacanth Latimeria the nickname "living fossil". This status generated much interest in both extinct and extant coelacanths leading to the production of numerous anatomical studies. However, detailed descriptions of extinct taxa are made difficult due to the quality of the fossil material which generally prevents fine comparisons with the extant Latimeria. Here we describe a new genus and species of coelacanth, Graulia branchiodonta gen. et sp. nov. from the Middle Triassic of Eastern France, based on microtomographical imaging using synchrotron radiation. Through exquisite 3D preservation of the specimens, we reconstructed the skeletal anatomy of this new species at an unprecedented level of detail for an extinct coelacanth, and barely achieved for the extant Latimeria. In particular, we identified a well-developed trilobed ossified lung whose function is still uncertain. The skeletal anatomy of G. branchiodonta displays the general Bauplan of Mesozoic coelacanths and a phylogenetic analysis resolved it as a basal Mawsoniidae, shedding light on the early diversification of one of the two major lineages of Mesozoic coelacanths. However, despite its exquisite preservation, G. branchiodonta carries a weak phylogenetic signal, highlighting that the sudden radiation of coelacanths in the Early and Middle Triassic makes it currently difficult to detect synapomorphies and resolve phylogenetic interrelationships among coelacanths in the aftermath of the great Permo-Triassic biodiversity crisis.

The lungfish, the extant sister group of the tetrapods, have an evolutionary history illustrated by a fossil record extending for ∼420 million years. The post-Paleozoic fossil record of the clade is almost exclusively restricted to sediments deposited in freshwater paleoenvironments and is characterized by an abundance of highly mineralized tooth plates, whereas cranial and postcranial remains are scarce. Here, we report a sample of isolated tooth plates found in the Upper Triassic Pebbly Arkose Formation of the Mid-Zambezi Basin, Zimbabwe. It consists of pterygoid and prearticular tooth plates from adult individuals, plus some dental plates referred to juvenile individuals, which we refer to a new species of Ferganoceratodus. This discovery provides an opportunity to review briefly the tooth plates of the ‘ptychoceratodontid morphotype’ reported from around the world. We discuss how various occurrences previously referred to Ptychoceratodus may be more appropriately referred, with caution, to Ferganoceratodus. We also describe the histology of the tooth plates of the new species and note similarities with other Mesozoic taxa. The scarcity of histological data for Mesozoic lungfish tooth plates compounds the problem of assigning isolated tooth plates to genus and species level. Ferganoceratodus and closely related taxa arose in the Early Triassic in southern Gondwana and diversified worldwide in the Late Triassic. The genus then became more common in Laurasia during the Jurassic and Early Cretaceous and declined thereafter with relict Late Cretaceous occurrences in Madagascar and South America.

Fossil evidence suggests that ray-finned fishes (Actinopterygii) diversified greatly after the largest mass extinction event at the Permian–Triassic boundary. This radiation resulted in a diversity peak in the Middle Triassic, which is manifested in diverse feeding specializations, especially among small-bodied Neopterygii. We present new material from an early Spathian (Early Triassic) outcrop in northern Dobrogea, southeast Romania. The material includes isolated jaw and palatal bones that evidently belong to a single individual, a durophagous actinopterygian, and isolated scales referred to the same taxon. A systematic evaluation of this material indicates affinities with †Polzbergiidae, and provides a first glimpse of internal aspects of the feeding apparatus of that group. A pair of ectopterygoids with crushing dentition show a well-developed lateral process, a feature that was previously proposed to be a synapomorphy uniting Cladistia (bichirs) with the Triassic †Scanilepiformes. The recognition of this structure in various Triassic ray-fins (summarized herein) indicates that it was probably widespread among stem neopterygians. The new material belongs to a large individual with a heterodont dentition, therefore representing the earliest large, specialized, durophagous neopterygian. It increases the group's morphological diversity in the Spathian, and hints at an earlier trophic diversification after the mass extinction. Based on new data, we analyse changes in body size of bony fishes through the Early and Middle Triassic. Current evidence suggests that body size distribution remained skewed towards larger sizes in the late Early Triassic, and that the diversification of small-bodied stem neopterygians had not yet been in full swing.

This work presents the first record of bony fish from the Maastrichtian of the Marília Formation (Bauru Group) in Goiás State, Brazil. A fragment of a pectoral spine, recovered by screen-washing, clearly represents an important catfish (Siluriformes) record from the Late Cretaceous of South America. The material possesses similarities with forms from the Campanian - early-Maastrichtian of the Adamantina Formation and the Maastrichtian of the Marília (São Paulo State) and El Molino (Bolivia) formations. Inclusion of the new material from Goiás in the dataset for the aforementioned areas within a paleoenvironmental setting provides evidence that Late Cretaceous catfish had a wider distribution than previously known.

The vertebrate skull varies widely in shape, accommodating diverse strategies of feeding and predation. The braincase is composed of several flat bones that meet at flexible joints called sutures. Nearly all vertebrates have a prominent 'coronal' suture that separates the front and back of the skull. This suture can develop entirely within mesoderm-derived tissue, neural crest-derived tissue, or at the boundary of the two. Recent paleontological findings and genetic insights in non-mammalian model organisms serve to revise fundamental knowledge on the development and evolution of this suture. Growing evidence supports a decoupling of the germ layer origins of the mesenchyme that forms the calvarial bones from inductive signaling that establishes discrete bone centers. Changes in these relationships facilitate skull evolution and may create susceptibility to disease. These concepts provide a general framework for approaching issues of homology in cases where germ layer origins have shifted during evolution.