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ABSTRACT AimStudies assessing large‐scale patterns of microbial diversity have predominantly focused on free‐living microorganisms, often failing to link observed patterns to established theories regarding the maintenance of global diversity patterns. We aimed to determine whether foliar fungi on two closely related grass hosts—Heteropogon contortusandThemeda triandra—display a commonly observed latitudinal gradient in species richness and determine whether host identity, energy (temperature and precipitation), climate seasonality, fire frequency and grass evolutionary history drive the observed patterns in species richness and composition. LocationPaleotropical. Time PeriodContemporary. Major Taxa StudiedFoliar fungi. MethodsFoliar fungal diversity was quantified from 201 leaf samples ofT. triandraandH. contortuscollected across the distributional range of these species. Mixed effects models were used to quantify patterns of diversity and their correlates among and within continents. Ordinations were used to assess drivers of composition. ResultsFoliar fungi displayed consistent latitudinal diversity gradients in richness. Energy was a strong driver of richness at inter‐continental and continental scales, while other factors had inconsistent impacts on richness among scales, hosts and guilds. Globally, richness was higher in regions of higher growing season temperatures and where hosts were present for longer periods. Composition was primarily structured by geographic region at the global scale, indicating that distance was a dominant driver of community composition. Within Australia, temperature and rainfall seasonality and the amount of growing season rainfall, were the dominant drivers of both richness and composition. Main ConclusionsWe find some support for the idea that foliar fungal species diversity is governed by the same factors as many macro‐organisms (energy availability and evolutionary history) at inter‐continental scales, but also that fungal diversity and composition in the highly seasonal continent of Australia were driven by factors that shape tropical grassy ecosystems, namely climate seasonality and fire. 

Abstract Angiosperms are the cornerstone of most terrestrial ecosystems and human livelihoods^1,2. A robust understanding of angiosperm evolution is required to explain their rise to ecological dominance. So far, the angiosperm tree of life has been determined primarily by means of analyses of the plastid genome^3,4. Many studies have drawn on this foundational work, such as classification and first insights into angiosperm diversification since their Mesozoic origins^5–7. However, the limited and biased sampling of both taxa and genomes undermines confidence in the tree and its implications. Here, we build the tree of life for almost 8,000 (about 60%) angiosperm genera using a standardized set of 353 nuclear genes⁸. This 15-fold increase in genus-level sampling relative to comparable nuclear studies⁹provides a critical test of earlier results and brings notable change to key groups, especially in rosids, while substantiating many previously predicted relationships. Scaling this tree to time using 200 fossils, we discovered that early angiosperm evolution was characterized by high gene tree conflict and explosive diversification, giving rise to more than 80% of extant angiosperm orders. Steady diversification ensued through the remaining Mesozoic Era until rates resurged in the Cenozoic Era, concurrent with decreasing global temperatures and tightly linked with gene tree conflict. Taken together, our extensive sampling combined with advanced phylogenomic methods shows the deep history and full complexity in the evolution of a megadiverse clade.