The skulls of archosaurs are morphologically and functionally diverse, with clade-specific specialized features that set apart crurotarsans (extant crocodilians and their stem lineage) from avemetatarsalians (birds and non-avian dinosaurs)1,2,3,4,5,6,7, as reviewed by Brusatte et al.8. The evolution and diversification of the skull of archosaurs have been associated with changes in the patterns of phenotypic integration and modularity9,10,11,12,13. For more information on integration and modularity in shape, see the review by Klingenberg14. Different regions of the skull may act as anatomical modules that can evolve, function, and develop semi-independently from one another. Bones within a same module tend to co-vary in shape and size more with each other than with bones from other such variational modules15,16,17,18. In addition, the bones of the skull can also modify their physical articulations so that some groups of bones are more structurally integrated than others, and, hence, we can recognize them as distinct anatomical-network modules, which had been defined by Eble as a type of organizational modules15,19,20. The relationship between anatomical-network modules and variational modules is not yet fully understood, but it is thought that network anatomy constrains growth patterns and shape variation21,22,23.

Changes in the anatomical organization of the skull in archosaurs have been concomitant with a broader evolutionary trend in tetrapods toward a reduction in the number of skull bones due to loses and fusions, a phenomenon known as the Williston’s law24,25,26. Understanding how the bones are globally arranged to each other allows us to measure the anatomical complexity and organization of body parts, and explain how structural constraints might have influenced the direction of evolution25,26,27,28. Werneburg et al. compared the skull network-anatomy of a highly derived Tyrannosaurus rex, Alligator mississippiensis and Gallus gallus with that of an opossum, a tuatara, and a turtle29. They found that the tyrannosaur has the most modular skull organization among these amniotes, with a modular separation of the snout in upper and lower sub-modules and the presence of a lower adductor chamber module. However, the specific anatomical changes in the organization of the archosaur skull during their evolutionary transitions more generally have never been characterized. More recently, Plateau and Foth used anatomical network analysis to study postnatal ontogenetic changes in the skulls of crown bird and non-avian theropods30. They found that early juvenile crown birds have skulls that are less integrated and more modular than those of more derived birds, resembling their non-avian theropod ancestors.

Here, we compared the anatomical organization and modularity of the skull of archosaurs using Anatomical Network Analysis (AnNA)31 to highlight how skull topology has changed in evolutionary and developmental scales. We chose AnNA over more conventional methods, such as geometric morphometrics, to understand how major re-organizations of the skull (i.e. loss and fusion of bones) affect the overall anatomy regardless of shape. We created network models of the skull for 21 species of archosaurs, including taxa representing key evolutionary transitions from early pseudosuchians to crocodiles, from non-avian theropods to modern birds, and from paleognath birds to neognaths. Our dataset also includes a representative ornithischian, a sauropodomorph, and a basal saurischian (Supplementary Information 1) for comparison. To understand the significance of the ontogenetic transitions in archosaur skulls, we provided our dataset with juvenile skulls for extant birds and alligator. Network models of the skull were built by coding individual cranial bones and their articulations with other bones as the nodes and links of a network, respectively (Fig. 1). Network modules, defined as a group of bones with more articulations among them than to other bones outside the module, were identified heuristically using a community detection algorithm. We compared skull architectures using topological variables (i.e. network parameters) that capture whole-skull anatomical feature (modelling and analysis of anatomical networks were detailed previously20,25,31).

Figure 1
figure 1

Anatomical network models. Example of the network models for three archosaurian skulls: (A) Aetosaurus from Schoch (2007)63; (B) Plateosaurus from Prieto-Marquez and Norell (2011)107; (C) Gallus from Digimorph. The pair-wise articulations among the bones of skulls (left) are formalized as network models (middle) and later analyzed, for example, to identify the skull anatomical node-based modules (right). See “Materials and methods” for details.

Networks and network modules and their respective complexity, integration, modularity, and anisomerism could be quantified by network parameters density of connections, clustering coefficient, path length, heterogeneity of connections, and parcellation20,23,31,32. Here, complexity is defined as the relationship of bones in a skull and is associated with how abundant are the interactions that bones have with each other (i.e. density of connections), how interdependent or integrated the bones are (i.e. clustering coefficient), and proximity between nodes (i.e. path length). A more complex network would have higher density, higher clustering coefficient, and shorter path length. Anisomerism is defined as a deviation among anatomical parts33 and could be observed by the specialization of bones and measured by heterogeneity of connections, i.e. how each bone has a different number of connection25. Modularity is measured by parcellation, which is the number of modules and the consistency in the number of bones per module.

Materials and methods


We sampled extinct and extant species, and for some forms included both adults and juveniles to account for ontogenetic trends within archosaurs. Namely, adults Aetosaurus ferratus, Archaeopteryx lithographica, Citipati osmolskae, Coelophysis bauri, Compsognathus longipes, Dakosaurus andiniensis, Desmatosuchus haplocerus, Dibothrosuchus elaphros, Dilophosaurus wetherilli, Eoraptor lunensis, Ichthyornis dispar, Plateosaurus engelhardti, Psittacosaurus lujiatunensis, Riojasuchus tenuisceps, Sphenosuchus acutus, Velociraptor mongoliensis, Gallus gallus, Geospiza fortis and Nothura maculosa; and juveniles Gallus gallus, Geospiza fortis, Nothura maculosa and Alligator mississippiensis. Within our sample set, eight species represent the transition from crurotarsan archosaur ancestor to modern crocodilians and 13 species represent the transition from non-avian theropods to modern birds as described previously34,35,36,37,38,39,40,41,42,43. Due to the sample size limitation for extinct taxa, reconstructed and type forms were used to represent each taxon and intraspecific variation could not be accounted for.

Phylogenetic context

We created a phylogenetic tree (Fig. 2) based on the previous studies34,35,36,37,39,40,41,42,43,44. The tree was calibrated using the R package paleotree45 by the conservative “equal” method46,47; branching events were constrained using the minimum dates for known internal nodes based on fossil data from Benton and Donoghue48 (listed in Supplementary Table S3) and the first and last occurrences of all 21 species from the Paleobiology Database using the paleobioDB package49 in R. Because there were two extinct Nothura species in the Paleobiology Database, the last occurrence for extant Nothura species was adjusted to 0 (Supplementary Table S2).

Figure 2
figure 2

Phylogenetic framework. A phylogenetic tree was created based on the evolutionary relations among taxa as detailed in previous work34,35,36,37,38,39,40,41,42,43. Bifurcation times were calibrated based on fossil dates from Benton and Donoghue48 using the equal method in the paleotree package45,46,47. First and last occurrences were from Paleobiology Database (details listed in Supplementary Table S2). Silhouettes were from See methods for details.

Network modelling

We built anatomical network models for each archosaur skull in our sample set based on detailed literature descriptions and CT scans of complete skulls (see Supplementary Information 1). Skull bones were represented as the nodes of the network model and their pair-wise articulations (e.g. sutures and synchondroses) were represented as links between pairs of nodes (Fig. 1). Skull network models were formalized as binary adjacency matrices, in which a 1 codes for two bones articulating and a 0 codes for absence of articulation. Bones that were fused together without trace of a suture in the specimens examined were formalized as a single individual bone.

Network analysis

Following Esteve-Altava et al.28, we quantified the following topological variables for each network model: the number of nodes (N), the number of links (K), the density of connections (D), the mean clustering coefficient (C), the mean path length (L), the heterogeneity of connections (H), the assortativity of connections (A), and the parcellation (P). The morphological interpretation of these topological variables has been detailed elsewhere28. A summary is provided here. N and K represent the direct count of the number of individual bones and articulations observed in the skull. D is the number of connections divided by the maximum number of possible connections (it ranges from 0 to 1); D is a proxy measure for morphological complexity. C is the average number of neighboring bones that connect to one another in a network (i.e., actual triangles of nodes compared to the maximum possible): a value close to 1 shows all neighboring bones connect to each other while a value close to 0 shows neighboring bones do not connect to each other; C is a proxy measure for anatomical integration derived from co-dependency between bones. L measures average number of links separating two nodes (it ranges from 1 to N − 1); L is a proxy measure of anatomical integration derived from the effective proximity between bones. H measures how heterogeneous connections are in a network: skulls composed of bones with a different number of articulations have higher H values. If all bones had the same number of connections (i.e., H = 0), it means that all bones were connected in the same way and the skull had a regular shape. A measures whether nodes with the same number of connections connect to each other (it ranges from − 1 to 1); H and A are a proxy measure for anisomerism or diversification of bones. P measures the number of modules and the uniformity in the number of bones they group (it ranges from 0 to 1); P is a proxy for the degree of modularity in the skull. Calculating P requires a given partition of the network into modules (see next below).

Network parameters were quantified in R50 using the igraph package51. Networks visualization was made using the visNetwork package52 and Cytoscape53.

Principal component analysis

We performed a Principal Component Analysis (PCA) of the eight topological variables with a singular value decomposition of the centered and scaled measures. On the resulting PCs, we used a PERMANOVA (10,000 iterations) to test whether topological variables discriminate between: (1) Avialae and non-Avialae; (2) adults and juveniles; (3) extinct and extant; (4) Crurotarsi and Avemetatarsalia; (5) Neornithes and non-Neornithes; (6) early flight, can do soaring flight, can do flapping flight, gliding, and flightless (details in Supplementary Table S5); (7) Crurotarsi, non-avian Dinosauria, and Aves; and (8) carnivorous, omnivorous, and herbivorous (dietary information in Supplementary Information 4). First, we performed the tests listed above for all archosaurs. Then, we repeated these tests for a sub-sample that included all archosaurs, except for all modern birds. Next, we repeated these tests for a sub-sample that included all archosaurs, except for adult birds.

Modularity analysis

To find the optimal partition into network modules we used a node-based informed modularity strategy54. This method starting with the local modularity around every individual node, using cluster_spinglass function in igraph51, then it returns the modular organization of the network by merging non-redundant modules and assessing their intersection statistically using combinatorial theory55.

Ethical approval

All methods were carried out in accordance with relevant guidelines and regulations from Imperial College ethics committee and were approved by Imperial College.


Topological discrimination of skull bones

A Principal Component Analysis (PCA) of the eight topological variables measured in skull network models discriminates skulls with different anatomical organizations (Supplementary Figs. S1S3). When all sampled skulls are compared together, the first three principal components (PCs) explain 89.4% of the total variation of the sample. PC1 (57.5%) discriminates skulls by number of their bones (N), density of connections (D), and degree of modularity (P). PC2 (21.3%) discriminates skulls by their degree of integration (C) and anisomerism (H). Finally, PC3 (10.6%) discriminates skulls by whether bones with similar number of articulations connect with each other (A).

PERMANOVA tests confirm that different skull anatomies map onto different regions of the morphospace. Thus, we can discriminate: Avialae (Aves plus Ichthyornis and Archaeopteryx) versus non-Avialae (F1,23 = 4.124, p = 0.006699; Fig. 3B); Neornithes plus toothless archosaurs versus archosaurs with teeth (F1,23 = 6.99, p = 0.0005999; Fig. 3C); Aves (include all modern birds) versus Crurotarsi versus non-avian Dinosauria (F2,22 = 3.837, p = 0.000699; Fig. 3D); and extant and extinct species (F1,23 = 4.304, p = 0.0017; Supplementary Fig. S1C). However, we find no statistically significant difference in morphospace occupation between crurotarsans and avemetatarsalians (F1,23 = 1.46, p = 0.2002, Supplementary Fig. S1D).

Figure 3
figure 3

Principal components decomposition of topological variables. (A) Skull distribution for each taxon (see labels below). (B) Comparison of Avialae versus non-Avialae shows that non-Avialae occupy part of the Avialae morphospace. (C) Comparison of Neornithes versus non-Neornithes shows that non-Neornithes overlap with part of the Neornithes morphospace. Orange dotted arrows show the ontogenetic change in modern birds from juvenile stage to adult stage. (D) Comparison of Aves, Crurotarsi, and Dinosauria shows that they occupied different morphospace. Ellipses show a normal distribution confidence interval around groups for comparison. Labels: N, Number of nodes; K, Number of links; D, Density of Connection; C, Mean clustering coefficient; H, Heterogeneity of connection; L, Mean path length; A, Assortativity of connection; P, Parcellation. Aeto, Aetosaurus; AllA, adult Alligator; AllJ, juvenile Alligator; Arcx, Archaeopteryx; Citi, Citipati; Coel, Coelophysis; Comp, Compsognathus; Croc, Crocodylus; Dako, Dakosaurus; Desm, Desmatosuchus; Dibo, Dibothrosuchus; Dilo, Dilophosaurus; Eora, Eoraptor; GalA, adult Gallus; GalJ, juvenile Gallus; GeoA, adult Geospiza; GeoJ, juvenile Geospiza; Icht, Ichthyornis; NotA, adult Nothura; NotJ, juvenile Nothura; Plat, Plateosaurus; Psit, Psittacosaurus; Rioj, Riojasuchus; Sphe, Sphenosuchus; Velo, Velociraptor. Silhouettes were from

When all avians are excluded from the comparison, the first three PCs now explain 80.6% of the total variation (Supplementary Figs. S4S6). PC1 (38.6%) discriminates skulls by the density of their inter-bone connections (D) and effective proximity (L). PC2 (22.6%) discriminates skulls by the number of bones and their articulations (N and K). Finally, PC3 (19.5%) now discriminates skulls by their anisomerism (H) and whether bones with the same number of connections connect to each (A). PERMANOVA tests could not discriminate between Crurotarsi and non-avian Dinosauria (F1,17 = 1.235, p = 0.3022; Supplementary Fig. S4D), and between extant and extinct species (F1,17 = 2.274, p = 0.06399; Supplementary Fig. S4C).

When only adult birds are excluded, the first three PCs explain 79.7% of the topological variation (Supplementary Figs. S7S9). PC1 (35.8%), PC2 (24.5%), and PC3 (19.5%) discriminate skull similarly as when all birds are excluded (see above). PERMANOVA tests also could not discriminate between juvenile birds, crurotarsans, and non-avian dinosaurs (F2,19 = 1.682, p = 0.09649; Supplementary Fig. S7D), and between extant and extinct species (F1,20 = 2.119, p = 0.06169; Supplementary Fig. S7C).

Regardless of the sub-sample compared, we found no statistically significant difference in morphospace occupation between taxa stratified by flying ability and diet (Supplementary Fig. S1E, see Supplementary Information 4 for details). This suggests that at least for the given sample set changes in cranial network-anatomy (i.e. how bones connect to each other) are independent of both dietary adaptations and the ability to fly.

Number of network modules

The number of network modules identified in archosaur skulls ranged from one (i.e. fully integrated skull) in adult birds Nothura maculosa (the spotted tinamou) and Geospiza fortis (medium ground finch) to eight in the non-avian dinosaur Citipati (Supplementary Table S10). The number of network modules within the studied taxa decreases during evolution of both major archosaurian clades: from 6 (Riojasuchus) to 4 (Desmatosuchus,) and from 6 (Dibothrosuchus) to 4 (Dakosaurus and all adult crocodilians) modules in Crurotarsi; from 6 (Coelophysis) to 4 (Dilophosaurus and Compsognathus), and from 8 (Citipati) to 4 (Velociraptor, Archaeopteryx, Ichthyornis, and juvenile modern birds) modules in theropod-juvenile bird transition (Fig. 4A,B, Supplementary Table S10). We found no modular division of the skull in adult Nothura and Geospiza. This is most likely because these skulls are highly integrated due to the extensive cranial bone fusion in adults, which, in turn, results in a network with very few nodes. In general, skull networks are partitioned into overlapping modules.

Figure 4
figure 4

Visualizations of the module composition changes across phylogeny. The number of node-based modules ranged from 1 to 8. (A) shows the changes in module composition from Riojasuchus to Crocodylus. (B) shows the changes in module composition from Coelophysis to Gallus. (C) shows the difference in module composition among the ornithischian Psittacosaurus, the basal saurischian Eoraptor, and the sauropodomorph Plateosaurus. (D) Comparisons of the adult and juvenile stages of extant species. Adult Nothura and Geospiza are shaded in grey as one module was identified because of the small number of nodes and links due to a highly fused skull. Nodes were colored based on their modules. Composition of each module is listed in Supplementary Table 4.


Occupation of morphospace and evolution of skull architecture

The two major groups of archosaurs (Crurotarsi and Avemetatarsalia) show an analogous trend towards a reduction in the number of skull bones (Supplementary Table S8; Supplementary Information 3), in line with the Williston’s Law, which states that vertebrate skulls tend to become more specialized with fewer bones as a result of fusions of neighboring bones during evolution25,56,57. This reduction in the number of bones and articulations, together with an increase in density, is also observed within aetosaurs and sphenosuchians (Supplementary Table S8). Likewise, we observed fusion of paired bones into new unpaired ones: for example, left and right frontals, parietals, and palatines are fused through their midline suture in the more derived taxa, such as the crocodilians (Supplementary Table S6). Bone fusion in extant species produced skulls that are more densely connected than the skulls of extinct species (Supplementary Fig. S1C). It was previously suggested that the more connected skulls would have more developmental and functional inter-dependences among bones, and, hence, they would be more evolutionarily constrained22,23. Similarly, avian cranium with its strongly correlated traits has lower evolutionary rates and bird skulls are less diverse overall12.

Bhullar et al. pointed out that avian kinesis relies on their loosely integrated skulls with less contact and, thus, skulls with highly overlapping bones would be akinetic58. This contradicts our observations here in that kinetic crown birds have more complex and integrated skulls than the akinetic crurotarsans and the partially kinetic Riojasuchus59. The reason could be that Bhullar et al. factored in how much connective tissue and number of contact points each bone has, but not the total number of connections possible from the number of bones in these taxa. The total number of articulations possible is the denominator used to calculate density. More recently, Werneburg and colleagues showed Tyrannosaurus, suspected to have kinesis, also has a higher density when compared to akinetic Alligator but lower density when compared to the more derived and clearly kinetic Gallus skull29.

When compared with modules identified by Felice et al.60, the node-based modules, such as the rostral and neurocranial modules (shown as blue and red modules in Fig. 4), are composed of elements essentially similar to those described as variational modules (more details in Supplementary Information 2). The supraoccipital and basioccipital bones were part of the same topology-defined (Supplementary Information 2, Fig. 4) and shape-defined module in most taxa, likely due to its functional importance in connecting the vertebral column with the skull60.


The aetosaurs, Aetosaurus and Desmatosuchus, and the sphenosuchians, Sphenosuchus and Dibothrosuchus, show an increase in complexity within their lineages. The more derived aetosaur Desmatosuchus has a fused skull roof (parietal fused with supraoccipital, laterosphenoid, prootic and opisthotic) and toothless premaxilla that are absent in the less derived aetosaur Aetosaurus61,62,63. In contrast, basal and derived sphenosuchian are more topologically similar. Their main difference is that basipterygoid and epiotic are separate in Sphenosuchus but are fused with other bones in the more derived Dibothrosuchus64,65. When we compared aetosaurs and sphenosuchians, we found that sphenosuchians have a skull roof intermediately fused condition between Aetosaurus and Dibothrosuchus: interparietal sutures in both sphenosuchians are fused while supraoccipital, laterosphenoid, opisthotic, and prootic remain separate.

To understand cranial topology in Thalattosuchia, a clade with adaptations specialized for marine life, we included Dakosaurus andiniensis. These adaptations comprise nasal salt glands66, hypocercal tail, paddle-like forelimbs, ziphodont dentition, fusion of the inter-premaxillary suture, a fused vomer, and a short and high snout67,68. Despite these adaptations, Dakosaurus has a cranial complexity closer to that of extant crocodilians by similarly having inter-frontal and inter-parietal fusions67,68. In addition to the fused frontals and parietals, both Crocodylus and Alligator have a fused palate and a fused pterygoid bones.

In turn, crurotarsans first fuse the skull roof and skull base, followed by the fusion of the face (more details on Supplementary Table S6). Interestingly, this resonates with the pattern of sutural fusion in alligator ontogeny, which cranial (i.e. frontoparietal) has the highest degree of suture closure followed by skull base (i.e. basioccipital-exoccipital) and then the face (i.e. internasal)69 suggesting that the same mechanism may control topological changes in both ontogeny and evolution.


Avemetatarsalian transition is marked with a faster ontogenetic bone growth in more derived taxa, indicated by higher degree of vascularization, growth marks, and vascular canal arrangement (reviewed by Bailleul70), more pneumatized skulls (reviewed by Gold71), and an increase in complexity reminiscent of what is observed in crurotarsans. The basal ornithischian Psittaosaurus lujiatunensis and basal saurischian Eoraptor lunensis are relatively close to each other on the morphospace (Fig. 3), with the Psittacosaurus skull showing slightly more density because of fused palatines, a trait which is also observed in extant crocodilians and some birds, and its extra rostral bone as observed in other ceratopsians72.

The basal sauropodomorph Plateosaurus engelhardti has the lowest clustering coefficient (i.e. lower integration) of archosaurs, suggesting that skulls of sauropodmorphs are less integrated than those of saurischians31, accompanied by poorly connected bones (as seen in the network in Fig. 4C). Poorly connected bones, for example epipterygoid, and some connections, such as the ectopterygoid-jugal articulation, are later lost in neosauropods43,73.

Within theropods, the ceratosaurian Coelophysis is more derived and has a slightly more complex and specialized skull than the ceratosaurian Dilophosaurus42. Their positions on the morphospace suggest that ceratosaurians occupy a region characterized by a higher mean path length (L), when compared to other archosaurs (Fig. 3). Compsognathus is close to Riojasuchus on the morphospace with a similar mean path length (Fig. 3 and Supplementary Fig. S4, Supplementary Table S8), its facial bones are also unfused, and it has a similar composition for its facial modules (see facial modules in Compsognathus and nasal modules in Riojasuchus on Supplementary Table S4 and Supplementary Fig. S10). These observations suggest an ancestral facial topology (see Supplementary Tables S6 and S8 for more details) is concomitant to the magnitude of shape change reported for compsognathids34. Compsognathus possesses an independent postorbital that is absent from Ichthyornis to modern birds. It also has an independent prefrontal that is absent in most Oviraptorsauria and Paraves74, including Citipati, Velociraptor, and from Ichthyornis to modern birds. Despite its ancestral features, the back of the skull and the skull base of Compsognathus are fused, similarly to other Paravians and modern birds.

The oviraptorid Citipati has a skull topology that occupies a morphospace within non-avian theropods, despite its unique vertically-oriented premaxilla and short beak34,75. Citipati has an independent epipterygoid that is also present in some non-avian theropods and ancestral archosaurs, such as Plateosaurus erlenbergiensis, but which is absent in extant archosaurs75,76,77,78. Citipati also has fused skull roof (with fused interparietals), skull base, and face, marked with fused internasal and the avian-like inter-premaxillary sutures.

Like other dromaeosaurids, Velociraptor’s eyes are positioned lateral to the rostrum. Its prefrontal bone is either absent or fused with the lacrimal while it remains separate in other dromaeosaurids79,80,81. We observed a loss of the prefrontals from Citipati to modern birds, but not in more ancestral archosaurs or crurotarsans. Bones forming the Velociraptor basicranium, such as basioccipital, and basisphenoid are fused with other members of the basicranium (listed in Supplementary Table S6). Despite having a similar number of bones and articulations to Citipati, the cranial bones in Velociraptor are more integrated with each other and are more likely to connect to bones with a different number of articulations (i.e. more disparity) (Supplementary Table S8). Like Compsognathus and other primitive non-avian dinosaurs, Velociraptor has an ancestral facial topology with separate premaxilla, maxilla, and nasal bones.

Archaeopteryx and Ichthyornis as intermediates between non-avian theropods and modern birds

The skull of Archaeopteryx occupied a region of the morphospace closer to non-avian dinosaurs and crurotarsans than to juvenile birds (Fig. 3). The distance of Archaeopteryx from crown birds and its proximity in the morphospace to Velociraptor and Citipati along the PC1 axis (Fig. 3) may reflect the evolving relationship between cranial topology and endocranial volume. In fact, Archaeopteryx has an endocranial volume which is intermediate between the ancestral non-avian dinosaurs and crown birds82,83 and it is within the plesiomorphic range of other non-avian Paraves84. This makes Archaoepteryx closer to dromaeosaurid Velociraptor than to oviraptor Citipati, for both its skull anatomy and its endocranial volume84. Modifications related to the smaller endocranial volume in Archaeopteryx include the unfused bones in the braincase, the independent reappearance of a separate prefrontal after the loss in Paraves74, a separate left and right premaxilla as observed in crocodilian snouts and ancestral dinosaurs, and the presence of separate postorbitals, which might restrict the fitting for a larger brain34.

Compared to Archaeopteryx, Ichthyornis is phylogenetically closer to modern birds and occupies a region of the morphospace near the juvenile birds and extant crocodilians when adult birds are included in the analysis (Fig. 3), but closer to extant crocodilians when all birds or when adult birds are removed (Supplementary Figs. S4S9). The proximity between Ichthyornis and juvenile birds may be explained by the similar modular division (as observed in Fig. 4B,D; Supplementary Table S4, Supplementary Fig. S10), presence of anatomical features characteristic of modern birds, such as the loss of the postorbital bones, the fusion of the left and right premaxilla to form the beak, a bicondylar quadrate that form a joint with the braincase, and the arrangement of the rostrum, jugal, and quadratojugal required for a functional cranial kinetic system58,85,86,87,88. The proximity between Ichthyornis and extant crocodilians in terms of complexity (Supplementary Figs. S4S9, Supplementary Table S8) may be explained by the fused frontal and fused parietal, and separate maxilla, nasal, prootic and laterosphenoid (Supplementary Table S6).

Paleognath and neognath birds

Juvenile birds have a skull roof with relatively less fused bones with the interfrontal, interparietal, and frontoparietal sutures open, and a more fused skull base. Postorbital is already fused in all juvenile birds (i.e. after hatching). Collectively, juvenile neognaths show a skull anatomy with a fused cranial base, relatively less fused roof, and unfused face that resembles the anatomy of ancestral non-avian theropods. Unlike what is observed in non-avian theropods, frontal, parietal, nasal, premaxilla, and maxilla eventually fuse with the rest of the skull in adult modern birds. However, in the palatal region not all the sutures are completely closed: the caudal ends of the vomers remained unfused in adult Nothura, which is a characteristic common in Tinamidae89. A similar pattern of suture closure has been described in another paleognath, the emu, in which the sutures of the base of the skull close first and then the cranial and facial sutures close while palatal sutures remain open69. The only difference is that in Nothura, where closure of major cranial sutures (frontoparietal, interfrontal, and interparietal) happens after the facial sutures closure. In summary, when compared with neognaths, the skull of the paleognath Nothura is more homogeneous and complex in both juvenile and adult stages. As the skull grows, its bones fuse and both its complexity and heterogeneity increase.

Within the neognaths, the skull of Geospiza fortis is more complex and more homogenous than Gallus gallus in both juvenile and adult stages: bones in Geospiza skull are more likely to connect with bones with the same number of connections than Gallus. These two trajectories illustrate how the connectivity of each bone diversifies and becomes more specialized within a skull as sutures fuse together, as predicted by the Williston’s law.

As in crurotarsans, major transitions in Avemetatarsalia are associated with the fusion first of the skull base, then the skull roof, and, finally, with the face (more details on Supplementary Table S6). This is more similar to the temporal pattern of sutural closure during ontogeny in the emu (skull base first, skull roof second, facial third) than to the one observed in the alligator (cranial first, skull base second, facial third)69, thus suggesting that the same mechanism for ontogeny may have been co-opted in Avemetatarsalia evolution.

Ontogenetic differences in topology between birds and crocodilians

Our comparisons on network anatomy found that juvenile birds occupy a region of the morphospace that is closer to the less derived archosaurs and crurotarsans than to that occupied by adult modern birds (Supplementary Fig. S1B). Juvenile birds have a degree of anisomerism of skull bones and skull anatomical complexity closer to that in crurotarsans and non-avian dinosaurs, while their pattern of integration overlaps with that of adult birds, crurotarsans, and non-avian dinosaurs. These similarities in complexity and heterogeneity may be explained by the comparably higher number and symmetrical spatial arrangements of circumorbital ossification centres in early embryonic stages74. For example, both crown avians and A. mississippiensis have two ossification centres that fuse into one for lacrimals74,90. Meanwhile, ossification centres that form the prefrontal and postorbital, fuse in prenatal birds but remain separate in adult non-avian dinosaurs74,90,91. These ossification centres later develop into different, but overlapping, number of bones and their arrangement in juvenile birds (27–34 bones) and adult non-avian theropods (32–44 bones) with discrepancies explained by the heterochronic fusion of the ossification centres (Supplementary Table S8).

Following postnatal fusions and growth, modern bird skulls become more heterogeneous and their bones more connected and topologically closer to each other (Figs. 3C and 5; Supplementary Table S8). This makes avian skull bones more diverse and functionally integrated. Simultaneously, skull topology in birds diversifies with ontogeny within their lineage, as shown by the ontogenetic trajectories of Gallus, Nothura, and Geospiza (Figs. 3C and 5). Thus, bones (1) develop from ossification centres shared among crurotarsans and avemetatarsalians, (2) interact as modules with heterogeneity and complexity similar to basal members at juvenile stage, and (3) then fuse and diversify to produce skulls of adult birds.

Figure 5
figure 5

Overview of the evolution of archosaurian skull topology: modern birds and few non-avian dinosaurs have more heterogeneous connections than crurotarsans; extant taxa have fewer bones and articulations than the extinct ones; bones in juvenile modern birds fuse and produce a more densely connected adult skull. Modules and networks of the following taxa are shown: (1) Gallus, (2) juvenile Gallus, (3) Plateosaurus, (4) Dilophosaurus, (5) Aetosaurus, (6) adult Alligator. Morphospace of Aves is significantly different from Crurotarsi and Dinosauria when adult birds are included. Orange arrows show the ontogenetic changes from juvenile to adult stages in neornithes. Taxa on the left side of the biplot have higher density and fewer bones, such as Gallus and Alligator, than taxa on the right, such as Aetosaurus and Dilophosaurus.

The skulls of birds, crocodilians, and dinosaurs develop from ossification centres with comparable spatial locations in the embryonic head74. When both evolutionary and ontogenetic cranial shape variation was compared among crocodilians, Morris and colleagues showed that at mid- to late embryonic stages, cranial shapes originated from a conserved region of skull shape morphospace92. They suggested that crocodilian skull morphogenesis at early and late embryonic stages are controlled by signaling molecules that are important in other amniotes as well, such as Bmp4, calmodulin, Sonic hedgehog (Shh); and Indian hedgehog92,93,94,95,96,97,98,99. Then, from late prenatal stages onward, snout of crocodilians narrows100 and elongates following different ontogenetic trajectories to give the full spectrum of crocodilian cranial diversity92.

Another major transformation in archosaurian evolution is the origin of skulls of early and modern birds from the snouted theropods. This transition involved two significant heterochronic shifts34,101. First, avians evolved highly paedomorphic skull shapes compared to their ancestors by developmental truncation34. This was followed, by a peramorphic shift where primitively paired premaxillary bones fused and the resulting beak bone elongated to occupy much of the new avian face101. By comparison, the skull of Alligator undergoes extensive morphological change and closing of the interfrontal and interparietal sutures during embryogenesis is followed by the prolonged postnatal and maturation periods, with the lack of suture closure and even widening of some sutures102,103. Bailleul et al. suggested that mechanisms that inhibit suture closure, rather than bone resorption, cause the alligator sutures to remain open during ontogeny103. Nevertheless, juvenile and adult alligators share the same cranial topology featuring similar module compositions and both occupy a region of morphospace close to Crocodylus (Fig. 4D and Supplementary Fig. S10; Supplementary Tables S4 and S8). Such topological arrangement suggests that conserved molecular, cellular, and developmental genetic processes underlie skull composition and topology observed across crocodilians. Likewise, oviraptorid dinosaurs, as represented by Citipati, display their own unique skull shape and ontogenetic transformation34, while retaining a topology conserved with other theropods. Combined, this evidence suggests that developmental mechanisms controlling skull composition and interaction among skull elements are conserved among theropods.

The process of osteogenesis underlies the shape and topology of the bony skull. In chicken embryo, inhibition of FGF and WNT signaling pathways prevented fusion of the suture that separates the left and right premaxilla, disconnected the premaxilla-palatine articulation and changed their shapes giving the distal face a primitive snout-like appearance101. The site of bone fusion in experimental unfused, snout-like chicken premaxillae showed reduced expression of skeletal markers Runx2, Osteopontin, and the osteogenic marker Col I101, implying localized molecular mechanisms regulating suture closure and shape of individual cranial bones. Thus, changes in gene expression during craniofacial patterning in avians95,96,98,104,105,106, non-avian dinosaurs, and crocodilians92,101 contribute to the clade-specific differences in skull anatomical organization resulting from the similar patterns of bone fusion of bones.

Finally, we observe some network modules where some bones within the same modules in juveniles will later fuse in adult birds, but not in A. mississippiensis (Supplementary Information 5; Fig. 4E and Supplementary Fig. S10, Supplementary Table S4). For example, in Nothura, premaxilla, nasal, parasphenoid, pterygoid, vomer, and maxilla grouped in the same juvenile module will later fuse during formation of the upper beak in the adult. In A. mississippiensis, premaxilla, maxilla, nasal, lacrimal, prefrontal, jugal, frontal, and ectopterygoid are also in the same juvenile module, but remain separate structures in adult. These findings suggest that bones within the same module may be more likely to fuse together in ontogeny but doing so is a lineage-specific feature.

Comparisons of juveniles and adults for extant birds and the alligator revealed ontogenetic changes linked to the evolution of the skull organization in archosaurs. Whereas the anatomical organization of the skull of juvenile alligators resembles that of adults, the anatomy of juvenile modern birds is closer to that of non-avian dinosaurs than to that of adult avians of the same species in terms of morphological complexity and anisomerism, probably due to the spatial arrangements of ossification centres at embryonic stages74,90,91. More specifically, the differences in skull organization between crown birds and non-avian dinosaurs could be explained by postnatal fusion of bones.


A network-based comparison of the cranial anatomy of archosaurs shows that differences within and among archosaurian clades are associated with an increase of anatomical complexity, a reduction in number of bones (as predicted by the Williston’s Law), and an increase of anisomerism marked by bone fusion, for both crurotarsans and avemetatarsalians. Our findings indicate that the anatomical organization of the skull is controlled by developmental mechanisms that diversified across and within each lineage: heterotopic changes in craniofacial patterning genes, heterochronic prenatal fusion of ossification centres74,90,91, and lineage-specific postnatal fusion of sutures. Some of these mechanisms have been shown to be conserved in other tetrapods. For example, heterotopy of craniofacial patterning genes also took place between chick and mice embryos95,96,106. Hu and Marcucio showed that mouse frontonasal ectodermal zone could alter the development of the avian frontonasal process, suggesting a conserved mechanism for frontonasal development in vertebrates96. Our findings illustrate how a comparative analysis of the anatomical organization of the skull can reveal both common and disparate patterns and processes determining skull evolution in vertebrates.