Search for: All records

Abstract Tropical elevation gradients support highly diverse assemblages, but competing hypotheses suggest either peak species richness in lowland rainforests or at mid‐elevations. We investigated scolytine beetles—phloem, ambrosia and seed‐feeding beetles—along a tropical elevational gradient in Papua New Guinea.Highly standardised sampling from 200 to 3700 m above sea level (asl) identified areas of highest and lowest species richness, abundance and other biodiversity variables.Using passive flight intercept traps at eight elevations from 200 to 3500 m asl, we collected over 9600 specimens representing 215 species. Despite extensive sampling, species accumulation curves suggest that diversity was not fully exhausted.Scolytine species richness followed a unimodal distribution, peaking between 700 and 1200 m asl, supporting prior findings of highest diversity at low‐to‐mid elevations.Alternative models, such as a monotonous decrease from lowlands to higher elevations and a mid‐elevation maximum, showed lesser fit to our data. Abundance is greatest at the lowest sites, driven by a few extremely abundant species. The turnover rate—beta diversity between elevation steps—is greatest between the highest elevations.Among dominant tribes—Dryocoetini, Xyleborini and Cryphalini—species richness peaked between 700 and 2200 m asl. Taxon‐specific analyses revealed distinct patterns:Euwallaceaspp. abundance uniformly declined with elevation, while other genera were driven by dominant species at different elevations.Coccotrypesand phloem‐feedingCryphalushave undergone evolutionary radiations in New Guinea, with many species still undescribed. Species not yet known to science are most likely to be found at lower and middle elevations, where overall diversity is highest. 

Abstract One mechanism proposed to explain high species diversity in tropical systems is strong negative conspecific density dependence (CDD), which reduces recruitment of juveniles in proximity to conspecific adult plants. Although evidence shows that plant-specific soil pathogens can drive negative CDD, trees also form key mutualisms with mycorrhizal fungi, which may counteract these effects. Across 43 large-scale forest plots worldwide, we tested whether ectomycorrhizal tree species exhibit weaker negative CDD than arbuscular mycorrhizal tree species. We further tested for conmycorrhizal density dependence (CMDD) to test for benefit from shared mutualists. We found that the strength of CDD varies systematically with mycorrhizal type, with ectomycorrhizal tree species exhibiting higher sapling densities with increasing adult densities than arbuscular mycorrhizal tree species. Moreover, we found evidence of positive CMDD for tree species of both mycorrhizal types. Collectively, these findings indicate that mycorrhizal interactions likely play a foundational role in global forest diversity patterns and structure. 

Abstract Arbuscular mycorrhizal (AM) and ectomycorrhizal (EcM) associations are critical for host-tree performance. However, how mycorrhizal associations correlate with the latitudinal tree beta-diversity remains untested. Using a global dataset of 45 forest plots representing 2,804,270 trees across 3840 species, we test how AM and EcM trees contribute to total beta-diversity and its components (turnover and nestedness) of all trees. We find AM rather than EcM trees predominantly contribute to decreasing total beta-diversity and turnover and increasing nestedness with increasing latitude, probably because wide distributions of EcM trees do not generate strong compositional differences among localities. Environmental variables, especially temperature and precipitation, are strongly correlated with beta-diversity patterns for both AM trees and all trees rather than EcM trees. Results support our hypotheses that latitudinal beta-diversity patterns and environmental effects on these patterns are highly dependent on mycorrhizal types. Our findings highlight the importance of AM-dominated forests for conserving global forest biodiversity.