Abstract
Following the Permo–Triassic mass extinction, Archosauriformes—the clade that includes crocodylians, birds, and their extinct relatives outside crown Archosauria—rapidly diversified into many distinct lineages, became distributed globally, and, by the Late Triassic, filled a wide array of resource zones. Current scenarios of archosauriform evolution are ambiguous with respect to whether their taxonomic diversification in the Early–Middle Triassic coincided with the initial evolution of dietary specializations that were present by the Late Triassic or if their ecological disparity arose sometime after lineage diversification. Late Triassic archosauriform dietary specialization is recorded by morphological divergence from the plesiomorphic archosauriform tooth condition (laterally-compressed crowns with serrated carinae and a generally triangular lateral profile). Unfortunately, the roots of this diversification are poorly documented, with few known Early–Middle Triassic tooth assemblages, limiting characterizations of morphological diversity during this critical, early period in archosaur evolution. Recent fieldwork (2007–2017) in the Middle Triassic Manda Beds of the Ruhuhu Basin, Tanzania, recovered a tooth assemblage that provides a window into this poorly sampled interval. To investigate the taxonomic composition of that collection, we built a dataset of continuous quantitative and discrete morphological characters based on in situ teeth of known taxonomic status (e.g., Nundasuchus, Parringtonia: N = 65) and a sample of isolated teeth (N = 31). Using crown heights from known taxa to predict tooth base ratio (= base length/width), we created a quantitative morphospace for the tooth assemblage. The majority of isolated, unassigned teeth fall within a region of morphospace shared by several taxa from the Manda Beds (e.g., Nundasuchus, Parringtonia); two isolated teeth fall exclusively within a “Pallisteria” morphospace. A non-metric multidimensional scaling ordination (N = 67) of 11 binary characters reduced overlap between species. The majority of the isolated teeth from the Manda assemblage fall within the Nundasuchus morphospace. This indicates these teeth are plesiomorphic for archosauriforms as Nundasuchus exhibits the predicted plesiomorphic condition of archosauriform teeth. Our model shows that the conservative tooth morphologies of archosauriforms can be differentiated and assigned to species and/or genus, rendering the model useful for identifying isolated teeth. The large overlap in tooth shape among the species present and their overall similarity indicates that dietary specialization lagged behind species diversification in archosauriforms from the Manda Beds, a pattern predicted by Simpson’s “adaptive zones” model. Although applied to a single geographic region, our methods offer a promising means to reconstruct ecological radiations and are readily transferable across a broad range of vertebrate taxa throughout Earth history.
Highlights
Adaptive radiations, or evolutionary diversifications, play a critical role in the history of life as clades speciate and fill new ecological roles over geologically rapid time intervals (Simpson, 1944; Schluter, 1996)
We present the first quantitative description of a Middle Triassic archosauriform tooth assemblage, which reveals substantial conservation of tooth morphology at the beginning of the archosaur radiation
NMT RB187, “Pallisteria,” and Parringtonia all display low disparity, but our sample includes only elements from a single individual of each taxon, whereas the Nundasuchus sample includes in situ teeth from one lower jaw and associated isolated teeth assigned to the holotype (Fig. 4)
Summary
Evolutionary diversifications, play a critical role in the history of life as clades speciate and fill new ecological roles over geologically rapid time intervals (Simpson, 1944; Schluter, 1996). In the former case species fill the same resource zones using similar, ancestral morphological structures (e.g., identical tooth morphologies), whereas in the latter each species would be expected to have a unique, derived morphology for its resource zone at the start of the radiation (for an empirical example, see Slater & Friscia, 2019). Determining which of these competing hypotheses operated in a case requires us to reconstruct an evolutionary radiation where a species-poor, adaptively restricted clade diversifies into a species-rich, adaptively disparate clade
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