Benjamin G. Freeman

Aim The exceptional turnover in biota with elevation and number of species coexisting at any elevation makes tropical mountains hotspots of biodiversity. However, understanding the historical processes through which species arising in geographical isolation (i.e. allopatry) assemble along the same mountain slope (i.e. sympatry) remains a major challenge. Multiple models have been proposed including (1) the sorting of already elevationally divergent species, (2) the displacement of elevation upon secondary contact, potentially followed by convergence, or (3) elevational conservatism, in which ancestral elevational ranges are retained. However, the relative contribution of these processes to generating patterns of elevational overlap and turnover is unknown. Location Tropical mountains of Central‐ and South‐America. Time Period The last 12 myr. Major Taxa Studied Birds. Methods We collate a dataset of 165 avian sister pairs containing estimates of phylogenetic age, geographical and regional elevational range overlap. We develop a framework based on continuous‐time Markov models to infer the relative frequency of different historical pathways in explaining present‐day overlap and turnover of sympatric species along elevational gradients. Results We show that turnover of closely related bird species across elevation can predominantly be explained by displacement of elevation ranges upon contact (81%) rather than elevational divergence in allopatry (19%). In contrast, overlap along elevation gradients is primarily (88%) explained by conservatism of elevational ranges rather than displacement followed by elevational expansion (12%). Main Conclusions Bird communities across elevation gradients are assembled through a mix of processes, including the sorting, displacement and conservatism of species elevation ranges. The dominant role of conservatism in explaining co‐occurrence of species on mountain slopes rejects more complex scenarios requiring displacement followed by expansion. The ability of closely related species to coexist without elevational divergence provides a direct and faster pathway to sympatry and helps explain the exceptional species richness of tropical mountains.

Aim The biotic interactions hypothesis predicts that interactions between species are stronger at lower elevations compared to higher elevations. We tested whether this prediction is met by examining elevational patterns in avian haemosporidian infections in New Guinean birds. Location YUS Conservation Area, Papua New Guinea. Taxon Birds and haemosporidia. Methods We collected blood samples from 2268 individuals of 66 bird species along a reef‐to‐ridgetop tropical elevational gradient covering ~3000 m of elevation. We used molecular methods to screen samples for haemosporidian parasites, and sequenced 70% of positive infections to determine the identity of parasite genera. We fit a phylogenetic generalized mixed‐effects model to test whether infection prevalence was higher at low elevations, as predicted by the biotic interactions hypothesis. Finally, we tested for phylogenetic signal in parasite prevalence and in host elevational distribution using Pagel's λ . Results Overall parasite prevalence was 45% . Infection prevalence decreased with elevation, though prevalence remained above ~30% even for high‐elevation communities between 2000 and 3000 m. We found strong phylogenetic signal in infection prevalence, but no phylogenetic signal in host elevational distribution. Nearly all sequenced infections (97%) were of Haemoproteus. Main Conclusions Our results are consistent with predictions arising from the biotic interactions hypothesis. However, phylogenetic relationships among hosts are a much better predictor of infection prevalence than is elevational position: closely related bird species tend to have similar infection prevalence regardless of the elevations where they live.