A persistent puzzle in vertebrate paleontology concerns the extraordinary taxonomic diversity achieved by pterosaurs — the flying reptiles that dominated Mesozoic skies — during the Late Cretaceous, a period when birds, their volant competitors, were simultaneously undergoing a rapid evolutionary radiation. An early and influential hypothesis attributed this co-flourishing to niche partitioning by body size: pterosaurs, it was argued, occupied the large-bodied aerial predator and scavenger roles, while birds diversified into small-bodied insectivorous and granivorous niches, thereby minimizing direct competition. The discovery of several giant azhdarchid pterosaur specimens from the Maastrichtian of Romania, with estimated wingspans exceeding ten meters, was long taken as compelling vindication of this size-partitioning model, since no contemporaneous bird approached such dimensions. Subsequent analysis of the Romanian fossil assemblages, however, has yielded a more complicated picture. The same deposits contain abundant small-bodied pterosaur taxa, including juvenile azhdarchids and diminutive pterodactyloids, whose jaw mechanics and dental microwear indicate diets — soft-bodied arthropods, small vertebrates — that overlap substantially with those of enantiornithine birds from the same strata. More tellingly, sedimentological evidence from the Hațeg Basin reveals that during the Maastrichtian, the region was an isolated island archipelago, an ecological setting in which resource limitation would have intensified, not relaxed, competitive pressures. The current understanding is that pterosaur-bird coexistence in these insular environments may have been facilitated not by clean niche separation but by the extreme ecological instability of the island system itself, which repeatedly disrupted community assembly and prevented any one clade from achieving lasting competitive exclusion.
1. The author discusses the giant azhdarchid pterosaur specimens from the Maastrichtian of Romania chiefly in order toA. identify the ecological mechanism that accounts for the prolonged coexistence of pterosaurs and birds during the Late Cretaceous
B. draw attention to an empirical finding that poses a difficulty for the niche-partitioning hypothesis
C. advance the claim that competitive exclusion cannot be the process responsible for pterosaur extinction at the end of the Cretaceous
D. recognize a body of evidence that appeared to corroborate a hypothesis the author goes on to complicate
E. present data that is fundamentally incompatible with the size-partitioning model of pterosaur-bird co-flourishing
2. The passage implies that the author would be most sympathetic to which of the following assessments of the size-partitioning hypothesis?A. It rests on a flawed presupposition about the temporal range over which pterosaurs and birds overlapped ecologically.
B. Its core contention is borne out by the discovery of giant azhdarchid specimens that vastly exceed contemporaneous birds in body size.
C. It offers an overly tidy account of the mechanisms by which volant vertebrate communities were structured during the Mesozoic.
D. It provides a persuasive explanation for pterosaur-bird coexistence on continental landmasses but fails to account for patterns observed in island ecosystems.
E. It exaggerates the significance of body-size divergence as a factor permitting the coexistence of ecologically similar taxa.