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Cardillo, M.

Publications and source records attributed to Cardillo, M..

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The ecological drivers of variation in global language diversity

Language diversity is distributed unevenly over the globe. Why do some areas have so many different languages and other areas so few? Intriguingly, patterns of language diversity resemble biodiversity patterns, leading to suggestions that similar mechanisms may underlie both linguistic and biological diversification. Here we present the first global analysis of language diversity that identifies the relative importance of two key ecological mechanisms suggested to promote language diversification - isolation and ecological risk - after correcting for spatial autocorrelation and phylogenetic non-independence. We find significant effects of climate on language diversity consistent with the ecological risk hypothesis that areas of high year-round productivity lead to more languages by supporting human cultural groups with smaller distributions. Climate has a much stronger effect on language diversity than landscape features that might contribute to isolation of cultural groups, such as altitudinal variation, river density, or landscape roughness. The association between biodiversity and language diversity appears to be an incidental effect of their covariation with climate, rather than a causal link between the two. While climate and landscape provide strong explanatory signal for variation in language diversity, we identify a number of areas of high unexplained language diversity, with more languages than would be predicted from environmental features alone; notably New Guinea, the Himalayan foothills, West Africa, and Mesoamerica. Additional processes may be at play in generating higher than expected language diversity in these regions.

ecology

Habitat loss is information loss: Species distribution models are compromised in anthropogenic landscapes

Species distribution models (SDMs) are valuable tools to estimate species distributions, but are vulnerable to biases in the probability of a species being observed. One such bias is habitat loss, which has affected a substantial and increasing proportion of the Earth. In regions of severe habitat loss, data on a species occurrence may represent a small, non-random subset of sites it once occupied. This could cause distorted reconstructions of species distributions, and misleading inferences of evolutionary and ecological processes. We present a statistical approach for quantifying the influence on SDMs of habitat loss, and generating distribution predictions that are robust to these biases. We explored some of the effects of accounting for habitat loss on inferences from common downstream biogeographic and ecological analysis methods.\n\nWe used herbarium record data to model the distribution of 325 plant species in the genera Banksia and Hakea across Australia, using point process models. We accounted for biases in the models by including a proxy variable representing habitat loss, and compared the fit of models without this variable to those with it. We explored the influence of habitat loss by mapping biodiversity patterns predicted with and without accounting for it.\n\nGenerally, accounting for habitat loss in SDMs led to increases in the mean area of modelled species distributions of ~10% for Banksia and ~12% for Hakea across Australia (in some cases, up to several 100,000 km2 increases in predicted range), with somewhat greater average increases (11% and 15%) for species in the southwest Australian biodiversity hotspot. Accounting for habitat loss leads to an increase in predicted species richness (Alpha and Gamma diversity), but a decrease in compositional turnover (Beta diversity), across most of Australia. Accounting for habitat loss in SDMs had minimal influence on a downstream macroevolutionary analysis (Age-Range Correlation) that utilizes species distributions, seemingly because exposure to habitat loss did not show a phylogenetic pattern in this taxonomic group.\n\nThe influence of habitat loss on species distributions estimated with SDM is likely to be context-dependent and difficult to generalize, but will tend to cause underestimates of range sizes. This may have consequences for mapping spatial patterns of diversity and for some downstream analyses of biogeographic, evolutionary, or ecological processes, based on species distributions, as well as conservation measures that rely on accurate species mapping.

ecology

Larger legume plants host a greater diversity of symbiotic nitrogen-fixing bacteria

A major goal in microbial ecology is to understand the factors that structure bacterial communities across space and time. For microbes that have symbiotic relationships with plants, an important factor that may influence their communities is host size or age, yet this has received little attention.\n\nUsing tree diameter size as a proxy for age, we quantified the diversity of rhizobia that associate with an endemic legume, Acacia acuminata, of variable size across a climate gradient in southwest Australia. We examined the 16S rRNA diversity (V1-V3 hypervariable region) of rhizobia at the taxonomic level and at higher sequence level diversity within taxonomic groups.\n\nWe identified 3 major taxonomic clades that associated with Acacia acuminata: Bradyrhizobiaceae, Rhizobiaceae, and Burkholderiaceae. Within these groups, we found extensive genetic variability, especially within Bradyrhizobiaceae. Using binomial multivariate statistical models that controlled for other factors that affect plant size and rhizobia community structure (climate and local soil characteristics), we determined that soil sampled at the base of larger Acacia trees was much more likely to contain a greater number of taxonomic clades and cryptic genetic variants within the Rhizobiaceae clade.\n\nDespite strong influences of climate and highly heterogeneous soil conditions on rhizobial diversity, our results show that host tree size is a prominent factor in structuring nitrogen-fixing symbionts diversity across a large landscape. The identification of a positive relationship between plant host size and microbial diversity raise interesting questions about the role of plant host size in driving ecological processes that govern microbial community assembly. Specifically, our results suggest that hosts may modify the habitat of their surrounding soil to enhance growth (niche construction hypothesis) or that symbiotic microbes have large differences in dispersal capability. Our results also suggest that host plants may be analogous to islands, where larger legume hosts may accumulate diversity over time, through migration opportunities or in situ diversification. From a practical perspective, including plant size as an additional variable may assist sampling and analyses designs of future soil microbial studies.

ecology