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INTRODUCTION Inherent in traditional views of ape origins is the idea that, like living apes, early large-bodied apes lived in tropical forests. In response to constraints related to locomoting in forest canopies, it has been proposed that early apes evolved their quintessential upright torsos and acrobatic climbing and suspensory abilities, enhancing their locomotor versatility, to distribute their weight among small supports and thus reach ripe fruit in the terminal branches. This feeding and locomotor transition from a quadruped with a horizontal torso is thought to have occurred in the Middle Miocene due to an increasingly seasonal climate and feeding competition from evolving monkeys. Although ecological and behavioral comparisons among living apes and monkeys provide evidence for versions of terminal branch forest frugivory hypotheses, corroboration from the early ape fossil record has been lacking, as have detailed reconstructions of the habitats where the first apes evolved. RATIONALE The Early Miocene fossil site of Moroto II in Uganda provides a unique opportunity to test the predictions of terminal branch forest frugivory hypotheses. Moroto II documents the oldest [21 million years ago (Ma)] well-established paleontological record of ape teeth and postcranial bones from a single locality and preserves paleoecological proxies to reconstruct the environment. The following lines of evidence from Moroto II were analyzed: (i) the functional anatomy of femora and a vertebra attributed to the ape Morotopithecus ; (ii) dental traits, including molar shape and isotopic profiles of Morotopithecus enamel; (iii) isotopic dietary paleoecology of associated fossil mammals; (iv) biogeochemical signals from paleosols (ancient soils) that reflect local relative proportions of C 3 (trees and shrubs) and C 4 (tropical grasses and sedges that can endure water stress) vegetation as well as rainfall; and (v) assemblages of phytoliths, microscopic plant-derived silica bodies that reflect past plant communities. RESULTS A short, strong femur biomechanically favorable to vertical climbing and a vertebra indicating a dorsostable lower back confirm that ape fossils from Moroto II shared locomotor traits with living apes. Both Morotopithecus and a smaller ape from the site have elongated molars with well-developed crests for shearing leaves. Carbon isotopic signatures of the enamel of these apes and of other fossil mammals indicate that some mammals consistently fed on water-stressed C 3  plants, and possibly also C 4  vegetation, in a woodland setting. Carbon isotope values of pedogenic carbonates, paleosol organic matter, and plant waxes all point to substantial C 4 grass biomass on the landscape. Analysis of paleosols also indicates subhumid, strongly seasonal rainfall, and phytolith assemblages include forms from both arid-adapted C 4 grasses and forest-indicator plants. CONCLUSION The ancient co-occurrence of dental specializations for leaf eating, rather than ripe fruit consumption, along with ape-like locomotor abilities counters the predictions of the terminal branch forest frugivory hypotheses. The combined paleoecological evidence situates Morotopithecus in a woodland with a broken canopy and substantial grass understory including C 4 species. These findings call for a new paradigm for the evolutionary origins of early apes. We propose that seasonal, wooded environments may have exerted previously unrecognized selective pressures in the evolution of arboreal apes. For example, some apes may have needed to access leaves in the higher canopy in times of low fruit availability and to be adept at ascending and descending from trees that lacked a continuous canopy. Hominoid habitat comparisons. Shown are reconstructions of a traditionally conceived hominoid habitat ( A ) and the 21 Ma Moroto II, Uganda, habitat ( B ). 

Throughout the Phanerozoic, estimated CO₂levels from CO₂proxies generally correlate well with independent estimates of temperature. However, some proxy estimates of atmospheric CO₂during the Late Cretaceous and early Paleocene are low (<400 ppm), seemingly at odds with elevated sea surface temperature. Here we evaluate early Paleocene CO₂by applying a leaf gas‐exchange model toPlatanitesleaves of four early Paleocene localities from the San Juan Basin, New Mexico (65.66–64.59 Ma). We first calibrate the model on two modernPlatanusspecies,Platanus occidentalisandP. × acerifolia, where we find the leaf gas‐exchange model accurately predicts present‐day CO₂, with a mean error rate between 5% and 14%. Applying the model to the early Paleocene, we find CO₂varies between ∼660 and 1,140 ppm. These estimates are consistent with more recent CO₂estimates from boron, leaf gas‐exchange, liverwort, and paleosol proxies that all suggest moderate to elevated levels of CO₂during the Late Cretaceous and early Paleocene. These levels of atmospheric CO₂are more in keeping with the elevated temperature during this period.

 

Palaeontological deposits on Rusinga Island, Lake Victoria, Kenya, provide a rich record of floral and faunal evolution in the early Neogene of East Africa. Yet, despite a wealth of available fossil material, previous palaeoenvironmental reconstructions from Rusinga have resulted in widely divergent results, ranging from closed forest to open woodland environments. Presented here is a detailed study of the sedimentology and fauna of the early Miocene Hiwegi Formation at Waregi Hill on Rusinga Island, Kenya. New sedimentological analyses demonstrate that the Hiwegi Formation records an environmental transition from the bottom to the top of the formation. Lower in the Hiwegi Formation, satin‐spar calcite after gypsum in siltstone deposits are interpreted as evidence for open hypersaline lakes. Moving up‐section, carbonate deposits – interpreted previously as evidence of aridity – are actually diagenetic calcite cements, which preserve root systems of trees, suggesting a more closed environment; further up‐section, the uppermost palaeosol layer contains abundant root traces and tree‐stump casts, previously reported as evidence of a closed‐canopy forest. These newly interpreted environmental differences are reflected by differences in faunal composition and abundance data from Hiwegi Formation fossil sites R1 and R3. Taken together, this work suggests that divergent palaeoenvironmental reconstructions in previous studies may have been informed by time‐averaging across multiple environments. Further, results demonstrate that during the early Miocene local or regional habitat heterogeneity already existed. Rusinga’s Hiwegi Formation varied both spatially and temporally, which challenges the interpretation that a broad forested environment stretched across the African continent during the early Neogene, transitioning later to predominately open landscapes that characterize the region today. This result has important implications for interpretations of the selective pressures faced by early Miocene fauna, including Rusinga Island’s well‐preserved fossil primates.

 

The cause of the end-Cretaceous mass extinction is vigorously debated, owing to the occurrence of a very large bolide impact and flood basalt volcanism near the boundary. Disentangling their relative importance is complicated by uncertainty regarding kill mechanisms and the relative timing of volcanogenic outgassing, impact, and extinction. We used carbon cycle modeling and paleotemperature records to constrain the timing of volcanogenic outgassing. We found support for major outgassing beginning and ending distinctly before the impact, with only the impact coinciding with mass extinction and biologically amplified carbon cycle change. Our models show that these extinction-related carbon cycle changes would have allowed the ocean to absorb massive amounts of carbon dioxide, thus limiting the global warming otherwise expected from postextinction volcanism.