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Evolutionary structure and timing of major habitat shifts in Crocodylomorpha


Extant crocodylomorphs are semiaquatic ambush predators largely restricted to freshwater or estuarine environments, but the group is ancestrally terrestrial and inhabited a variety of ecosystems in the past. Despite its rich ecological history, little effort has focused on elucidating the historical pattern of ecological transitions in the group. Traditional views suggested a single shift from terrestrial to aquatic in the Early Jurassic. However, new fossil discoveries and phylogenetic analyses tend to imply a multiple-shift model. Here we estimate ancestral habitats across a comprehensive phylogeny and show at least three independent shifts from terrestrial to aquatic and numerous other habitat transitions. Neosuchians first invade freshwater habitats in the Jurassic, with up to four subsequent shifts into the marine realm. Thalattosuchians first appear in marine habitats in the Early Jurassic. Freshwater semiaquatic mahajangasuchids are derived from otherwise terrestrial notosuchians. Within nearly all marine groups, some species return to freshwater environments. Only twice have crocodylomorphs reverted from aquatic to terrestrial habitats, both within the crown group. All living non-alligatorid crocodylians have a keratinised tongue with salt-excreting glands, but the lack of osteological correlates for these adaptations complicates pinpointing their evolutionary origin or loss. Based on the pattern of transitions to the marine realm, our analysis suggests at least four independent origins of saltwater tolerance in Crocodylomorpha.


Living crocodylomorphs (crown-group Crocodylia) are semiaquatic ambush predators largely restricted to freshwater or estuarine environments. However, the group is ancestrally terrestrial1 and has filled a wide variety of ecological niches in the past, in some ways comparable to Cenozoic mammals. Extinct crocodylomorphs include large fully marine taxa analogous to modern toothed whales (e.g., refs2,3), small terrestrial herbivores (e.g., refs4,5,6), and large terrestrial apex predators (e.g., refs7,8,9). Despite this ecological diversity, little is known about the timing or pattern of major habitat shifts within Crocodylomorpha.

Traditional views on crocodylomorph evolution posit a terrestrial origin, followed by a shift to a freshwater semiaquatic habitat early in the history of the group (e.g., refs10,11,12,13). From this freshwater semiaquatic phylogenetic core – what von Huene11 called the “fertile Stamm” – numerous crocodylomorph lineages moved into marine realms or shifted back onto land (Fig. 1). This traditional view established a single-shift model, with the transition from a terrestrial to an aquatic mode of life occurring early in the group’s history. For the purpose of this study our use of the term “aquatic” refers to taxa inhabiting either freshwater and marine habitats.

Figure 1
figure 1

Traditional hypotheses of crocodylomorph habitat transition underpinning the single-shift model. (a) The “fertile Stamm” – a freshwater, semiaquatic phylogenetic core from which multiple lineages independently shift to terrestrial or marine ecosystems (adapted from ref.11). (b) Spindle diagram of Langston12, depicting a single shift to the aquatic realm from “Protosuchia” to “Mesosuchia” in the Early Jurassic (adapted from ref.12). Green represents terrestrial habitats, gray/black represents freshwater semiaquatic, blue represents marine.

Decades of fossil discoveries and modern phylogenetic hypotheses call the single-shift model into question. While some disagreement among phylogenetic hypotheses remains, nearly all imply more than one transition from terrestrial to aquatic. The highly marine-adapted clade Thalattosuchia may either be deeply nested among other marine neosuchians or represent a group of very early diverging crocodylomorphs14,15,16,17,18. If thalattosuchians diverged early, this suggests at least two separate shifts from terrestrial to aquatic ecologies. Additionally, a number of Cretaceous Gondwanan crocodyliforms (e.g., Mahajangasuchus, Kaprosuchus, Stolokrosuchus) exhibit cranial adaptations typically found in definitively semiaquatic taxa such as elongate platyrostral or tube-like snouts, orbits located dorsally on the skull, and/or dorsally-facing external nares19,20,21. While the exact placement of these taxa can vary among competing phylogenetic hypotheses, they are generally recovered as part of the largely terrestrial notosuchian radiation22,23,24,25,26. These advances collectively suggest that a multiple-shift model better explains the pattern and timing of ecological shifts within Crocodylomorpha.

In addition to shifts from terrestrial to aquatic, some crocodylomorphs nested within aquatic clades appear to have reverted to non-aquatic habitats, and shifts from freshwater to marine environments potentially occurred numerous times. The ability to utilize marine environments is predicated on adaptations for saltwater tolerance. All living non-alligatorid crocodylians have a keratinised tongue with salt-excreting glands27,28,29, facilitating the use of marine habitats (even if some extant species are entirely restricted to freshwater environments today). Unfortunately, these adaptations in extant taxa do not leave osteological correlates, confounding attempts to pinpoint their origin in the fossil record. However, the persistent presence of certain fossil crocodylomorph taxa in marine sediments implies some type of adaptation for salt tolerance. Estimating where in crocodylomorph phylogeny these marine transitions occurred will help constrain when adaptations related to saltwater tolerance evolved.

Modern, large-scale analyses of crocodylomorph phylogeny are becoming increasingly common (e.g., refs18,23,30,31,32,33). By combining comprehensive phylogenetic hypotheses with habitat data, we reconstruct the evolutionary sequence of habitat shifts within Crocodylomorpha. Understanding this sequence of transitions is an important first step towards understanding the related morphological adaptations that accompany transitions to novel environments.


Tree Building and Time Calibration

We performed a new phylogenetic analysis based on the dataset of Wilberg34. Taxon sampling was increased to 100 taxa (8 outgroup and 92 ingroup) and character sampling increased to 407 (the phylogenetic data matrix, character descriptions, and materials referenced for character scoring are available in the Supplementary Information). The dataset was analyzed with TNT v1.535,36 using equally weighted parsimony. A heuristic search included 1000 replicates of Wagner trees using random addition sequences followed by TBR (tree bisection and reconnection) branch swapping holding 10 trees per replication. The shortest trees obtained from these replicates were subjected to a final round of TBR branch swapping to ensure all minimum length trees were discovered. Zero-length branches were collapsed if they lacked support under any of the minimal length trees (Rule 1 of Coddington and Scharff37).

To increase our coverage of Eusuchia for the ancestral habitat reconstruction analysis, we constructed an informal supertree by grafting of the topology of Eusuchia (based on refs31,38) onto the appropriate portion of the tree, resulting in a tree with 144 terminal taxa (including 49 crown-group taxa). To estimate branch lengths, we first compiled geological ages for all ingroup taxa. Ages for fossil occurrences were either set at stratigraphic midpoint values (typically at Stage level) or taken from absolute values of radioisotopic dates if available. These were obtained from the literature and/or via the Paleobiology Database (; stratigraphic data utilized in this study are available in Supplementary Information). Boundary ages follow Gradstein et al.39. The phylogeny was time-calibrated and branch lengths were generated using the geological age of the terminal taxa and temporally smoothed ghost lineage analysis, as outlined in Ruta et al.40 and subsequently used by various authors41,42,43,44. Time-calibrated trees were generated using the R45 software library ‘paleotree’46 with the “equal” option in the function TimePaleoPhy. Under the “equal” option, a value (vartime) must be provided that controls for the amount of time added to the root that will be used to smooth time along the unconstrained internodes. We chose a value corresponding to 5 million years. Choice of “vartime” value had little to no effect on reconstructed node ages. Our time-calibrated tree file is available in the Supplementary Information.

Ancestral Habitat Reconstruction

Each crocodylomorph species was assigned one of three broad habitat categories: terrestrial, freshwater semiaquatic, or marine. Most extant crocodylians are restricted to freshwater habitats. While some species of Crocodylus frequent marine environments (e.g. C. porosus), they inhabit predominantly freshwater and brackish environments. Thus, we chose to classify all extant crocodylians as freshwater. Habitat assignments of fossil crocodylomorphs were based on a combination of the depositional environment in which the fossils were found and their morphology. Taxa from terrestrial deposits (e.g. fluvial; lacustrine) were assigned as freshwater if they showed gross morphological similarity to extant semiaquatic crocodylians, or terrestrial if they possessed morphological features posited to correlate with terrestriality (e.g., dorsoventrally tall cranium, elongate limbs, well-developed 4th trochanter of the femur; refs9,22,47,48,49,50). Taxa found exclusively in marine sediments were assigned to the marine habitat category. Within the marine category, some taxa show adaptations for a fully pelagic lifestyle (e.g. hypocercal tail fin, paddle-like limbs; refs2,3,18). However, for this study we have chosen to group these taxa with semiaquatic coastal marine species. Ancestral states were reconstructed in Mesquite v3.1051 using maximum likelihood (ML) under a Mk model.

Sensitivity Analyses

Assignment of habitat to the Early Jurassic Calsoyasuchus valliceps is somewhat difficult. Calsoyasuchus is found in fluvial deposits of the Kayenta Formation of Arizona, which contain both terrestrial and river-dwelling vertebrates52. The skull of Calsoyasuchus is broadly similar to those of freshwater semiaquatic crocodyliforms (elongate snout, orbits relatively dorsally positioned), yet it also possesses several features characteristic of terrestrial forms, such as a dorsoventrally tall cranium and serrated dentition. To test the impact of the habitat assignment of this taxon on our results we ran separate analyses with Calsoyasuchus designated as terrestrial and as freshwater semiaquatic.

To test the effect of phylogenetic uncertainty on the pattern of habitat shifts, we also performed a number of analyses based on alternative tree topologies. Our phylogenetic analysis recovered Calsoyasuchus as the sister taxon to Hsisosuchus – to our knowledge, a novel topology. All prior published analyses recovered Calsoyasuchus as a goniopholidid. Thus, we also reran our analysis with Calsoyasuchus as the basal-most member of Goniopholididae (as in refs30,32). As noted earlier, the phylogenetic position of Thalattosuchia is contentious. To test the robustness of our results to the phylogenetic position of Thalattosuchia, we also performed our analyses on trees in which Thalattosuchia is sister to other marine neosuchians (Tethysuchia), or as basal mesoeucrocodylians (sister-group to Metasuchia as in refs3,21). Stolokrosuchus is sometimes recovered as more closely related to Neosuchia than to Notosuchia. Thus, we ran our analyses on a tree in which Stolokrosuchus is the sister-taxon to Neosuchia (as in ref.20). Finally, molecular analyses of crocodylian phylogeny consistently recover Gavialis as sister to Tomistoma, rather than as the basal-most lineage of the group. To test the effect of the molecular hypothesis on our results, we ran analyses in which Gavialis and Tomistoma are extant sister taxa, one excluding thoracosaurs and another including them. Exclusion of thoracosaurs reflects the temporal results of most molecular analyses; Late Cretaceous through Paleocene thoracosaurs predate the divergence time between Gavialis and Tomistoma supported by most molecular analyses (e.g., refs53,54,55). Combined analyses of molecular and morphological data (e.g., refs56,57) support a gavialoid affinity for thoracosaurs. Time calibrated tree files for sensitivity analyses are available in the Supplementary Information.


For ancestral state reconstructions, only the most likely state will be noted unless its likelihood is less than 90%. See Supplementary Information for node by node likelihood scores.

Ancestral habitat reconstruction

Reconstructing ancestral habitats across the tree results in a large number of independent transitions between environments (Fig. 2). Crocodylomorphs made the transition from terrestrial to aquatic habitats at least three times: (1) at the origin of Thalattosuchia in the Early Jurassic; (2) at the origin of Neosuchia in the Middle/Late Jurassic; (3) at the origin of the clade Stolokrosuchus + Mahajangasuchidae (within the otherwise terrestrial clade Notosuchia) in the Cretaceous. If Calsoyasuchus is, in fact, freshwater semiaquatic, this would require a fourth transition from terrestrial to freshwater in the Early Jurassic.

Figure 2
figure 2

Phylogenetic and temporal pattern of habitat shifts within Crocodylomorpha. Colored arrows within circles indicate habitat transitions. Horizontal arrows indicate habitat transitions that occurred within collapsed groups. Combined green and black coloring of Calsoyasuchus represents uncertainty regarding its assigned habitat. Note that internal branches are scaled to make the figure legible, not according to the chronograms we employed in the analysis.

At least nine shifts between freshwater and marine habitats occur throughout Crocodylomorpha (five from freshwater to marine; four from marine to freshwater; Fig. 2). These will be discussed on a clade-by-clade basis. Thalattosuchia is reconstructed with a habitat shift from terrestrial to marine at its origin (Fig. 3). A later shift from marine to freshwater occurred in the common ancestor of the Peipehsuchus + Phu Noi teleosaurid clade in the Early Jurassic.

Figure 3
figure 3

Phylogenetic and temporal pattern of habitat shifts within Thalattosuchia. Colored arrows within circles indicate habitat transitions. Ancestral state reconstructions at all nodes >0.9 in favor of one habitat. Note that internal branches are scaled to make the figure legible, not according to the chronograms we employed in the analysis.

The pattern of transitions within Tethysuchia is more complex, with multiple shifts from freshwater to marine habitats and one shift from marine back to freshwater (Fig. 4). Tethysuchia is reconstructed as ancestrally freshwater, with the common ancestor of Dyrosauridae reconstructed as making the transition to a marine habitat (86.0% marine; 13.3% freshwater). Within Dyrosauridae, a clade of South American taxa (Cerrejonisuchus + Anthracosuchus) reverted to a freshwater habitat. Pholidosaurids are ancestrally freshwater, and the two marine taxa (Oceanosuchus, Terminonaris) represent independent invasions of the marine realm (Fig. 4).

Figure 4
figure 4

Phylogenetic and temporal pattern of habitat shifts within Tethysuchia. Colored arrows within circles indicate habitat transitions. Pie chart at Dyrosauridae node indicates relative support for each habitat (shown only for nodes where ancestral state is reconstructed with a likelihood <0.9). Note that internal branches are scaled to make the figure legible, not according to the chronograms we employed in the analysis.

Within Crocodylia, two independent transitions from freshwater to marine habitats occur: one at the base of Gavialoidea in the Late Cretaceous and one at the base of Tomistominae in the Eocene (Fig. 5). The two living representatives of these clades, Gavialis gangeticus and Tomistoma schlegelii, are limited to freshwater, representing separate reversions from marine environments.

Figure 5
figure 5

Phylogenetic and temporal pattern of habitat shifts within Crocodylia. Colored arrows within circles indicate habitat transitions. Ancestral state reconstructions at all nodes >0.9 in favor of one habitat. Note that internal branches are scaled to make the figure legible, not according to the chronograms we employed in the analysis.

Only twice have crocodylomorphs reverted from an aquatic to a highly terrestrial habit, both instances occurring within the crown group (Fig. 5). The planocraniids appear to have become terrestrial predators in the early Paleogene (though our phylogenetic hypothesis requires them to diverge from other crocodylian lineages in the Late Cretaceous). The second shift back to the terrestrial realm involves the Miocene mekosuchine Quinkana. Interestingly, we see no shifts from terrestrial back to aquatic within Neosuchia.

The terrestriality of Notosuchia is reconstructed as an ancestral characteristic retained from earlier crocodylomorphs (75.9% terrestrial; 23.9% freshwater; Figs 2, 6). Within Notosuchia, a single transition to freshwater occurred (at the base of the Mahajangasuchidae + Stolokrosuchus clade) in the Early Cretaceous (Aptian).

Figure 6
figure 6

Phylogenetic and temporal pattern of habitat shifts within Notosuchia. Colored arrows within circles indicate habitat transitions. Pie chart at basal node indicates relative support for each habitat (shown only for nodes where ancestral state is reconstructed with a likelihood <0.9). Note that internal branches are scaled to make the figure legible, not according to the chronograms we employed in the analysis.

Sensitivity Analyses

Results of the sensitivity analyses support the multiple-shift model (i.e. multiple shifts from terrestrial to aquatic). The alternative phylogenetic hypotheses tested result in slight differences in the timing and pattern of shifts, but only one supports the single-shift model (while implying additional aquatic to terrestrial shifts). For full results of the topological sensitivity analyses, including node-by-node likelihood scores, see the Supplementary Information.

To test the impact of habitat assignment for Calsoyasuchus, we ran separate analyses for terrestrial and freshwater. Scoring Calsoyasuchus as freshwater semiaquatic impacted some nearby nodes. The node bounding Mesoeucrocodylia + Calsoyasuchus/Hsisosuchus was still reconstructed as terrestrial, but with lower likelihood (78.8% terrestrial; 21.1% freshwater). The freshwater semiaquatic habitat assignment of Calsoyasuchus also affected the node bounding Neosuchia + Notosuchia, reducing the previously strong level of confidence in the inference of terrestriality for the node, but maintaining terrestrial as most likely (58.7% terrestrial; 41.1% freshwater).

Placing Calsoyasuchus as a goniopholidid results in only one major change – an additional transition from freshwater semiaquatic to terrestrial (if Calsoyasuchus is considered terrestrial). This would represent the only transition from freshwater to terrestrial outside of the crown group. This placement of Calsoyasuchus also reduces confidence in the reconstruction of a freshwater habitat at the base of Neosuchia (30.7% terrestrial; 67.3% freshwater), at the basal node of Goniopholididae (29.8% terrestrial; 70.2% freshwater), and at the node joining Goniopholididae with other neosuchians (27.6% terrestrial; 72. 4% freshwater).

If thalattosuchians are basal mesoeucrocodylians (sister to Notosuchia + Neosuchia), the number of transitions from terrestrial to aquatic is reduced to two: once at the base of the clade containing Thalattosuchia + other mesoeucrocodlyians (reconstructed as a terrestrial to marine transition) and once in mahajangasuchids. This renders habitat reconstruction at the node bounding Notosuchia + Neosuchia ambiguous, with a slight lean towards freshwater (25.7% terrestrial; 43.9% freshwater; 30.4% marine). Placing thalattosuchians as sister to other marine neosuchians (Tethysuchia) also reduces the number of terrestrial to aquatic transitions to two (one at the origin of Neosuchia and one at the origin of the Stolokrosuchus + Mahajangasuchidae clade). The habitat reconstruction for the node bounding Notosuchia + Neosuchia is ambiguous between terrestrial and freshwater (47.8% terrestrial; 51.8% freshwater), and confidence in the terrestriality of the common ancestor of Notosuchia is also reduced (67.8% terrestrial; 32.1% freshwater). If the common ancestor of Notosuchia inhabited freshwater, this would make the freshwater habitat of Stolokrosuchus + Mahajangasuchidae a retention of the ancestral notosuchian habitat, which would require the peirosaurids to make an independent transition from freshwater to terrestrial. This scenario reduces the overall number of transitions from terrestrial to freshwater to one and increases the number of aquatic to terrestrial transitions to three (one outside the crown group).

Positioning Stolokrosuchus as a basal neosuchian, rather than as sister to Mahajangasuchidae, has little impact on our results. The terrestriality of Notosuchia is even more strongly reconstructed as the retention of an ancestral habitat preference (88.4% terrestrial; 21.5% freshwater), and mahajangasuchids are still recovered as making an independent transition from terrestrial to freshwater.

Trees in which tomistomines and thoracosaurs are gavialoids reduce the number of freshwater to marine transitions in the crown group to one, but have no significant impact on any other reconstructed transitions. If tomistomines are gavialoids but thoracosaurs are not, we still reconstruct two independent transitions from freshwater to marine within or near the crown group (one in thoracosaurs and one at the root of Gavialidae). Under both scenarios, the freshwater habitat of modern Gavialis and Tomistoma represents the result of two independent transitions.


Crocodylomorphs are well known for exhibiting extensive convergent evolution, especially with respect to the cranium11,12,13,34,58. Unsurprisingly, much of this convergence accompanies ecological shifts, when relatively distantly related lineages adapt to the same habitats. Repeated invasion of the aquatic realm produced broadly convergent skull and body shapes – though each group elaborated or reduced features independently. When ancestrally semi-aquatic crocodylians (e.g., Planocraniidae) shifted back into the terrestrial realm, they developed cranial adaptations reminiscent of the large, predatory notosuchians (e.g., Baurusuchidae, Sebecidae) such as dorsoventrally tall snouts, mediolaterally compressed, serrated dentitions, and enlarged caniniform teeth.

The five crocodylomorph groups that independently transitioned into the marine realm (Thalattosuchia, Dyrosauridae, Pholidosauridae, Gavialoidea, and Tomistominae) share similar morphological adaptations primarily related to snout shape (i.e. an elongate slender snout). Interestingly, these groups are involved in two of the largest phylogenetic controversies in Crocodylomorpha: the Gavialis/Tomistoma debate57,59,60,61 and the “longirostrine problem” involving the phylogenetic relationship between thalattosuchians and tethysuchians15,17,18,60,62. This suggests potential morphological convergence related to marine adaptation may be obscuring phylogenetic signal.

Within each of the marine groups (with the possible exception of Pholidosauridae) some species returned to freshwater environments. This includes the extant Gavialis gangeticus and Tomistoma schlegelii. Although found only in freshwater settings today, both are derived independently from ancestors found in marginal marine deposits (Fig. 5). This is true whether they are distantly related (e.g., refs59,63,64) or living sister lineages, as supported by molecular and some morphometric data (e.g., refs57,61,65). Both gavialoids and tomistomines have geographic distributions that only make sense if marine barriers were crossed multiple times, including a crossing of the Atlantic during the late Paleogene by close Gavialis relatives58,66. Gavialoids may have made the transition from marine to freshwater twice, as Gavialis and some Neotropical gharials related to Gryposuchus (not included in our analysis) must have been separately derived from marginal marine ancestors67.

Only twice in crocodylomorph history have groups reverted from an aquatic to a terrestrial habit, both occurring within the crown group - the planocraniids and the mekosuchine Quinkana. The planocraniid excursion to the terrestrial realm occurs in the early Cenozoic, possibly in response to open niches provided by the end-Cretaceous mass extinction. Quinkana inhabited Australia and persisted until the early Quaternary in the absence of terrestrial placental predators.

Among notosuchians, only one major habitat shift occurred (terrestrial to freshwater semiaquatic). However, an additional major ecological transition occurred in terrestrial members of this clade in the absence of a habitat shift – a transition from terrestrial carnivore to omnivore/herbivore. A number of notosuchian taxa exhibit tightly occluding heterodont dentitions reminiscent of mammals (e.g., Pakasuchus5, sphagesaurids6). Others possessed dentitions mimicking herbivorous reptiles (e.g., Simosuchus4,68). These excursions into omnivory and herbivory occurred in the Cretaceous of Gondwana and may represent the filling of vacant ecological niches due to the relative paucity of mammals and small ornithischian dinosaurs in Gondwana during this time period6.

While we can infer saltwater tolerance in fossil lineages found in marine and estuarine deposits, the lack of good osteological correlates makes the assignment of said adaptations to a particular node of the tree difficult. The exception to this may be Thalattosuchia. Some metriorhynchids preserve three-dimensional endocasts of large antorbital structures interpreted as hypertrophied salt glands69,70,71,72,73. Osteological correlates related to these putative antorbital salt glands include an enlarged internal carotid system and a preorbital foramen, presumably for drainage of the gland72,73. Enlarged internal carotid systems exist in some form across Thalattosuchia, suggesting that salt tolerance is ancestral for the clade74,75, though a preorbital foramen is unique to derived metriorhynchoids (see76 for additional discussion of this topic).

Only two published thalattosuchians are known from freshwater deposits: Peipehsuchus and an unnamed taxon from Phu Noi, Thailand. Martin et al.77 performed strontium isotope ratio analyses on the undescribed fossils from Phu Noi to test the habitat of these teleosaurids. The Phu Noi teleosaurids fell within the range of other continental vertebrates, suggesting that they were long-term residents of continental freshwater environments and did not migrate between marine and freshwater habitats. Peipehsuchus, another Asian teleosaurid, is also reported from freshwater lacustrine deposits78. In our analysis, these two taxa form a clade nested well within Teleosauridae, and are thus derived from a marine ancestor (Fig. 3). This nested position of freshwater forms suggests that thalattosuchians are either ancestrally marine, skipping over an intermediate freshwater semiaquatic stage during their transition from the terrestrial to marine realm, or that specimens preserving a freshwater stage exist, but are yet to be recovered.

Our results indicate that salinity tolerance likely evolved independently in dyrosaurids and the marine pholidosaurids Oceanosuchus and Terminonaris (Fig. 4). However, it is also possible that salinity tolerance may have arisen once in their last common ancestor and that basal pholidosaurids, like modern crocodylids, possessed adaptations for salt tolerance but generally preferred freshwater habitats.

Within Crocodylia, all living non-alligatorids, including the gharials, have a keratinised tongue with salt-excreting glands. Alligatorid historical biogeography suggests a much smaller number of dispersal events across marine barriers than occurred in other crocodylian groups, consistent with the diminished salinity tolerance observed in living forms79. That close outgroups to Crocodylia tend to be geographically restricted80 suggests that the alligatorid condition is plesiomorphic. If true, this requires that salinity tolerance evolved at least twice within the crown group – once in the common ancestor of Gavialoidea and once along the stem of Crocodyloidea. Unfortunately, the lack of osteological correlates for the keratinised tongue and lingual salt glands precludes determination of whether freshwater semiaquatic stem crocodyloid taxa such as Prodiplocynodon or Brachyuranochampsa possessed these features. Salt tolerance must have evolved at least by the common ancestor of tomistomines and crocodylines.


The long evolutionary history of Crocodylomorpha includes a number of independent major transitions between terrestrial, freshwater, and marine habitats. These transitions are not unidirectional. With the exception of marine to terrestrial, all possible transitions occurred at least once in the group’s history. Elucidating where these transitions occurred in the phylogenetic history of the group represents an important first step to investigating the associated phenotypic changes that accompany major habitat shifts.

Data Availability

All data generated or analysed during this study are included in this published article (and its Supplementary Information files).


  1. Parrish, J. M. The origin of crocodilian locomotion. Paleobiology 13, 396–414 (1987).

    Article  Google Scholar 

  2. Young, M. T. et al. The cranial osteology and feeding ecology of the metriorhynchid crocodylomorph genera Dakosaurus and Plesiosuchus from the Late Jurassic of Europe. PLoS One 7, e44985, (2012a).

    ADS  CAS  Article  PubMed  PubMed Central  Google Scholar 

  3. Young, M. T., Brusatte, S. L., Beatty, B. L., Andrade, M. B. & Desojo, J. B. Tooth-on-tooth interlocking occlusion suggests macrophagy in the Mesozoic marine crocodylomorph Dakosaurus. Anat. Rec. 295, 1147–1158 (2012b).

    Article  Google Scholar 

  4. Buckley, G. A., Brochu, C. A., Krause, D. W. & Pol, D. A pug-nosed crocodyliform from the Late Cretaceous of Madagascar. Nature 405, 941–944 (2000).

    ADS  CAS  Article  Google Scholar 

  5. Marinho, T. S. & Carvalho, I. S. An armadillo-like sphagesaurid crocodyliform from the Late Cretaceous of Brazil. J. S. Am. Earth Sci. 27, 36–41 (2009).

    Article  Google Scholar 

  6. O’Connor, P. M. et al. The evolution of mammal-like crocodyliforms in the Cretaceous period of Gondwana. Nature 466, 748–751 (2010).

    ADS  Article  Google Scholar 

  7. Carvalho, I. S., Campos, A. C. A. & Nobre, P. H. Baurusuchus salgadoensis, a new Crocodylomorpha from the Bauru Basin (Cretaceous), Brazil. Gondwana Res. 8, 11–30 (2005).

    ADS  Article  Google Scholar 

  8. Zanno, L. E., Drymala, S., Nesbitt, S. J. & Schneider, V. P. Early crocodylomorph increases top tier predator diversity during rise of dinosaurs. Sci. Rep.-UK 5, 9276 (2015).

    ADS  CAS  Article  Google Scholar 

  9. Godoy, P. L. et al. Postcranial anatomy of Pissarrachampsa sera (Crocodyliformes, Baurusuchidae) from the Late Cretaceous of Brazil: insights on lifestyle and phylogenetic significance. PeerJ 4, e2075, (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  10. Fraas, E. Die Meer-Krocodilier (Thalattosuchia) des oberen Jura unter specieller Berücksichtigung von Dacosaurus und Geosaurus. Palaeontographica 49, 1–72 (1902).

    Google Scholar 

  11. Huene, F. von. Ein Versuch zur Stammesgeschichte der Krokodile. Centralblatt für Mineralogie, Geologie und Paläontologie, Abteilung B. 11, 577–585 (1933).

    Google Scholar 

  12. Langston, W. The crocodilian skull in historical perspective. Biology of the Reptilia. Vol. 4. (eds Gans, C. & Parsons, T.) 263–284 (Academic Press, 1973).

  13. Buffetaut, E. Radiation évolutive, paléoécologie et biogéographie des crocodiliens mésosuchiens. Mém. S. Géo. F. 142, 1–88 (1982).

    Google Scholar 

  14. Clark, J. M. Phylogenetic relationships of the crocodylomorph archosaurs. Unpublished Ph.D. Dissertation. 556 pp (University of Chicago, 1986).

  15. Clark J. M. Patterns of evolution in Mesozoic Crocodyliformes. In the Shadow of the Dinosaurs. Early Mesozoic Tetrapods. (eds Fraser, N. C. & Sues, H.-D.) 84–97 (Cambridge University Press, 1994).

  16. Jouve, S. The skull of Teleosaurus cadomensis (Crocodylomorpha; Thalattosuchia), and phylogenetic analysis of Thalattosuchia. J. Vertebr. Paleontol. 29, 88–102 (2009).

    Article  Google Scholar 

  17. Pol, D. & Gasparini, Z. Skull anatomy of Dakosaurus andiniensis (Thalattosuchia: Crocodylomorpha) and the phylogenetic position of Thalattosuchia. J. Syst. Palaeontol. 7, 163–197 (2009).

    Article  Google Scholar 

  18. Wilberg, E. W. What’s in an outgroup? The impact of outgroup choice on the phylogenetic position of Thalattosuchia (Crocodylomorpha) and the origin of Crocodyliformes. Syst. Biol. 64, 621–637 (2015a).

    CAS  Article  Google Scholar 

  19. Larsson, H. C. E. & Gado, B. A new Early Cretaceous crocodyliform from Niger. Neues Jahrb. Geol P.-A. 217, 131–141 (2000).

    Google Scholar 

  20. Turner, A. H. & Buckley, G. A. Mahajangasuchus insignis (Crocodyliformes: Mesoeucrocodylia) cranial anatomy and new data on the origin of the eusuchian-style palate. J. Vertebr. Paleontol. 28, 382–408 (2008).

    Article  Google Scholar 

  21. Sereno, P. C. & Larsson, H. C. E. Cretaceous crocodyliforms from the Sahara. Zookeys 28, 1–143 (2009).

    Article  Google Scholar 

  22. Pol, D., Leardi, J. M., Leucona, A. & Krause, M. Postcranial anatomy of Sebecus icaeorhinus (Crocodyliformes, Sebecidae) from the Eocene of Patagonia. J. Vertebr. Paleontol. 32, 328–354 (2012).

    Article  Google Scholar 

  23. Pol, D. et al. A new notosuchian from the Late Cretaceous of Brazil and the phylogeny of advanced notosuchians. PLoS One 9, e93105, (2014).

    ADS  CAS  Article  PubMed  PubMed Central  Google Scholar 

  24. Sertich, J. J. W. & O’Connor, P. M. A new crocodyliform from the middle Cretaceous Galula Formation, southwestern Tanzania. J. Vertebr. Paleontol. 34, 576–596 (2014).

    Article  Google Scholar 

  25. Leardi, J. M., Pol, D., Novas, F. E. & Riglos, M. S. The postcranial anatomy of Yacarerani boliviensis and the phylogenetic significance of the notosuchian postcranial skeleton. J. Vertebr. Paleontol. (2015).

  26. Fiorelli, L. E. et al. A new Late Cretaceous crocodyliform from the western margin of Gondwana (La Rioja Province, Argentina). Cretaceous Res. 60, 194–209 (2016).

    Article  Google Scholar 

  27. Taplin, L. E. & Grigg, G. C. Salt glands on the tongue of the estuarine crocodile. Science 212, 1045–1047 (1981).

    ADS  CAS  Article  Google Scholar 

  28. Taplin, L. E. & Grigg, G. C. Historical zoogeography of the eusuchian crocodilians: a physiological perspective. Am. Zool. 29, 885–901 (1989).

    Article  Google Scholar 

  29. Grigg, G. & Kirshner, D. Biology and Evolution of Crocodylians. (Cornell University Press, 2015).

  30. Andrade, M. B., Edmonds, R., Benton, M. J. & Schouten, R. A new Berriasian species of Goniopholis (Mesoeucrocodylia, Neosuchia) from England, and a review of the genus. Zool. J. Linn. Soc.-Lond. 163, S66–S108 (2011).

    Article  Google Scholar 

  31. Brochu, C. A. Phylogenetic relationships of Palaeogene ziphodont eusuchians and the status of Pristichampsus Gervais, 1853. Earth Env. Sci. T. R. So. 103, 521–550 (2013).

    Google Scholar 

  32. Turner, A. H. & Pritchard, A. C. The monophyly of Susisuchidae (Crocodyliformes) and its phylogenetic placement in Neosuchia. PeerJ 3, e759, (2015).

    Article  PubMed  PubMed Central  Google Scholar 

  33. Young, M. T., Hastings, A. K., Allain, R. & Smith, T. J. Revision of the enigmatic crocodyliform Elosuchus felixi de Lapparent de Broin, 2002 from the Lower-Upper Cretaceous boundary of Niger: potential evidence for an early origin of the clade Dyrosauridae. Zool. J. Linn. Soc. 179, 377–403 (2016).

    Google Scholar 

  34. Wilberg, E. W. Investigating patterns of crocodyliform cranial disparity through the Mesozoic and Cenozoic. Zool. J. Linn. Soc. 181, 189–208 (2017).

    Article  Google Scholar 

  35. Goloboff, P. A., Farris, J. & Nixon, K. TNT: a free program for phylogenetic analysis. Cladistics 24, 774–786 (2008).

    Article  Google Scholar 

  36. Goloboff, P. A. & Catalano, S. A. TNT version 1.5, including a full implementation of phylogenetic morphometrics. Cladistics 32, 221–238, (2016).

    Article  Google Scholar 

  37. Coddington, J. A. & Scharff, N. Problems with zero-length branches. Cladistics 10, 415–423 (1994).

    Article  Google Scholar 

  38. Brochu, C. A., Njau, J., Blumenschine, R. J. & Densmore, L. D. A new horned crocodile from the Plio-Pleistocene hominid sites at Olduvai Gorge, Tanzania. PLoS ONE 5, e9333, (2010).

    ADS  CAS  Article  PubMed  PubMed Central  Google Scholar 

  39. Gradstein, F. M., Ogg, J. G., Schmitz, M. D. & Ogg, G. M. The Geologic Time Scale 2012 (Elsevier, 2012)

  40. Ruta, M., Wagner, P. J. & Coates, M. I. Evolutionary patterns in early tetrapods. I. Rapid intitial diversification followed by decrease in rates of character change. P. Roy. Soc. Lond. B. Bio. 273, 2107–2111 (2006).

    Article  Google Scholar 

  41. Brusatte, S. L., Benton, M. J., Ruta, M. & Lloyd, G. T. Superiority, competition, and opportunism in the evolutionary radiation of dinosaurs. Science 321, 1485–1488 (2008).

    ADS  CAS  Article  Google Scholar 

  42. Nesbitt, S. et al. A complete skeleton of a Late Triassic saurischian and the early evolution of dinosaurs. Science 326, 1530–1533 (2009).

    ADS  CAS  Article  Google Scholar 

  43. Turner, A. H. & Nesbitt, S. J. Body size evolution during the Triassic archosauriform radiation. Anatomy, Phylogeny and Palaeobiology of Early Archosaurs and their Kin. (eds Nesbitt, S. J., Desojo, J. B. & Irmis, R. B.) 573–597 (The Geological Society), (2013).

  44. Turner, A. H., Pritchard, A. C. & Matzke, N. J. Empirical and Bayesian approaches to fossil-only divergence times: A study across three reptile clades. PLoS One 12, e0169885 (2017).

    Article  Google Scholar 

  45. R Core Team. R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria. (2015).

  46. Bapst, D. A. paleotree: an R package for paleontological and phylogenetic analyses of evolution. Methods Ecol. Evol. 3, 803–807 (2012).

    Article  Google Scholar 

  47. Gasparini, Z., Fernández, M. & Powell, J. New Tertiary sebecosuchians (Crocodylomorpha) from SouthAmerica: phylogenetic implications. Hist. Biol. 7, 1–19 (1993).

    Article  Google Scholar 

  48. Busbey, A. B. The structural consequences of skull flattening in crocodilians. Functional Morphology in Vertebrate Paleontology (ed. Thomason, J.) 173–92 (Cambridge University Press, 1995).

  49. Rossmann, T. Studien an känozoischen Krokodilen: 5. Biomechanische Untersuchung am poskranialen Skelett des paläogenen Krokodils Pristichampsus rollinatii (Eusuchia: Pristichampsidae). Neues Jahrb. Geol P.-A. 217, 289–330 (2000).

    Google Scholar 

  50. Farlow, J. O., Hurlburt, G. R., Elsey, R. M., Britton, A. R. C. & Langston, W. J. Femoral dimensions and body size of Alligator mississippiensis: estimating the size of extinct mesoeucrocodylians. J. Vertebr. Paleontol. 25, 354–369 (2005).

    Article  Google Scholar 

  51. Maddison, W. P. & Maddison, D. R. Mesquite: A modular system for evolutionary analysis. Version 3.04. (2015).

  52. Tykoski, R. S., Rowe, T. B., Ketcham, R. A. & Colbert, M. W. Calsoyasuchus valliceps, a new crocodyliform from the Early Jurassic Kayenta Formation of Arizona. J. Vertebr. Paleontol. 22, 593–611 (2002).

    Article  Google Scholar 

  53. Hass, C. A., Hoffman, M. A., Densmore, L. D. & Maxson, L. R. Crocodilian evolution: insights from immunological data. Mol. Phylogenet. Evol. 1, 193–201 (1992).

    CAS  Article  Google Scholar 

  54. Roos, J., Aggarwal, R. K. & Janke, A. Extended mitogenomic phylogenetic analyses yield new insight into crocodylian evolution and their survival of the Cretaceous-Tertiary boundary. Mol. Phylogenet. Evol. 45, 663–673 (2007).

    CAS  Article  Google Scholar 

  55. Oaks, J. R. A time-calibrated species tree of Crocodylia reveals a recent radiation of the true crocodiles. Evolution 65, 3285–3297 (2011).

    Article  Google Scholar 

  56. Brochu, C. A. & Densmore, L. D. Crocodile phylogenetics: A review of current progress Crocodilian Biology and Evolution. (eds Grigg, G., Seebacher, F. & Franklin, C. E.) 3–8 (Surrey Beatty and Sons, 2001).

  57. Gatesy, J., Amato, G., Norell, M. A., DeSalle, R. & Hayashi, C. Combined support for wholesale taxic atavism in gavialine crocodylians. Syst. Biol. 52, 403–22 (2003).

    Article  Google Scholar 

  58. Brochu, C. A. Crocodylian snouts in space and time: phylogenetic approaches toward adaptive radiation. Am. Zool. 41, 564–585 (2001).

    Google Scholar 

  59. Brochu, C. A. Morphology, fossils, divergence timing, and the phylogenetic relationships of Gavialis. Syst. Biol. 46, 479–522 (1997).

    CAS  Article  Google Scholar 

  60. Brochu, C. A. Future directions in archosaur phylogenetics. J.Paleontol. 75, 1185–1201 (2001).

    Article  Google Scholar 

  61. Gold, M. E. L., Brochu, C. A. & Norell, M. A. An Expanded Combined Evidence Approach to the Gavialis Problem Using Geometric Morphometric Data from Crocodylian Braincases and Eustachian Systems. PLoS ONE 9, e105793, (2014).

    ADS  CAS  Article  PubMed  PubMed Central  Google Scholar 

  62. Jouve, S., Iarochéne, M., Bouya, B. & Amaghzaz, M. A new species of Dyrosaurus (Crocodylomorpha, Dyrosauridae) from the early Eocene of Morocco: phylogenetic implications. Zool. J. Linn. Soc.-Lond. 148, 603–656 (2006).

    Article  Google Scholar 

  63. Norell, M. A. The higher level relationships of the extant Crocodylia. J. Herpetol. 23, 325–335 (1989).

    Article  Google Scholar 

  64. Jouve, S., Bouya, B., Amaghzaz, M. & Meslouh, S. Maroccosuchus zennaroi (Crocodylia: Tomistominae) from the Eocene of Morocco: phylogenetic and palaeobiogeographical implications of the basalmost tomistomine. J. Syst. Palaeontol. 13, 421–445 (2015).

    Article  Google Scholar 

  65. Densmore, L. D. Biochemical and immunological systematics of the order Crocodylia. Evol. Biol. 15, 397–465 (1983).

    Article  Google Scholar 

  66. Velez-Juarbe, J., Brochu, C. A. & Santos, H. A gharial from the Oligocene of Puerto Rico: transoceanic dispersal in the history of a non-marine reptile. Proc. R. Soc. B 274, 1245–1254, (2007).

    Article  PubMed  Google Scholar 

  67. Salas-Gismondi, R. et al. A new 13 million year old gavialoid crocodylian from proto-Amazonian mega-wetlands reveals parallel evolutionary trends in skull shape linked to longirostry. PLoS One 11, e0152453 (2016).

    Article  Google Scholar 

  68. Kley, N. J. et al. Craniofacial morphology of Simosuchus clarki (Crocodyliformes: Notosuchia) from the Late Cretaceous of Madagascar. J. Vertebr. Paleontol. 30, 13–98 (2010).

    Article  Google Scholar 

  69. Fernández, M. & Gasparini, Z. Salt glands in a Tithonian metriorhynchid crocodyliform and their physiological significance. Lethaia 33, 269–276 (2000).

    Article  Google Scholar 

  70. Fernández, M. S. & Gasparini, Z. Salt glands in the Jurassic metriorhynchid Geosaurus: implications for the evolution of osmoregulation in Mesozoic marine crocodyliforms. Naturwissenshaften 95, 79–84 (2008).

    ADS  Article  Google Scholar 

  71. Gandola, R., Buffetaut, E., Monaghan, N. & Dyke, G. Salt glands in the fossil crocodile Metriorhynchus. J.Vertebr. Paleontol. 26, 1009–1010 (2006).

    Article  Google Scholar 

  72. Fernández, M. S. & Herrera, Y. Paranasal sinus system of Geosaurus araucanensis and the homology of the antorbital fenestra in metriorhynchids (Thalattosuchia: Crocodylomorpha). J. Vertebr. Paleontol. 29, 702–714 (2009).

    Article  Google Scholar 

  73. Herrera, Y., Fernández, M. S. & Gasparini, Z. The snout of Cricosaurus araucanensis: a case study in novel anatomy of the nasal region of metriorhynchids. Lethaia 46, 331–340 (2013).

    Article  Google Scholar 

  74. Wilberg, E. W. A new metriorhynchoid (Crocodylomorpha, Thalattosuchia) from the Middle Jurassic of Oregon and the evolutionary timing of marine adaptations in thalattosuchian crocodylomorphs. J. Vertebr. Paleontol. 35, e902846, (2015b).

    Article  Google Scholar 

  75. Brusatte, S. L. et al. The braincase and neurosensory anatomy of an Early Jurassic marine crocodylomorph: implications for crocodylian sinus evolution and sensory transitions. Anat. Rec. 299, 1511–30 (2016).

    Article  Google Scholar 

  76. Pierce, S. E., Williams, M. & Benson, R. B. J. Virtual reconstruction of the endocranial anatomy of the early Jurassic marine crocodylomorph Pelagosaurus typus (Thalattosuchia). PeerJ 5, e3225, (2017).

    Article  PubMed  PubMed Central  Google Scholar 

  77. Martin, J. E. et al. Strontium isotopes and the long-term residency of thalattosuchians in the freshwater environment. Paleobiology 42, 143–56 (2015).

    Article  Google Scholar 

  78. Wang, Q. -W. et al. Paleoenvironmental reconstruction of Mesozoic dinosaur faunas in Sichuan Basin. 189 pp. (Geology Press, Beijing, 2008).

  79. Tarailo, D. A., Hester, D. & Brochu, C. A. Oceanic dispersal rates within Crocodylia and their significance to the development of salt tolerance in crocodyloids. J. Vertebr. Paleontol. Program and Abstracts, 2017, 203 (2017).

    Google Scholar 

  80. Narváez, I., Brochu, C. A., Escaso, F., Pérez-García, A. & Ortega, F. New crocodyliforms from southwestern Europe and definition of a diverse clade of European Late Cretaceous basal eusuchians. PLoS One 10, e0140679, (2015).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

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We thank the Stony Brook Evolutionary Biology Discussion Group for providing valuable feedback and criticism of an earlier version of this work. AHT was supported by NSF DEB 1257485 and NSF DEB 1754596. CAB was supported by NSF DEB 1257786-125748. EWW was supported by NSF Doctoral Dissertation Improvement Grant DEB 1011097 and by NSF DEB 1754596.

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E.W.W. designed the project, analyzed the data, and wrote the manuscript. A.H.T. analyzed the data and wrote the manuscript. C.A.B. provided data and wrote the manuscript.

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Correspondence to Eric W. Wilberg.

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Wilberg, E.W., Turner, A.H. & Brochu, C.A. Evolutionary structure and timing of major habitat shifts in Crocodylomorpha. Sci Rep 9, 514 (2019).

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