Dung removal increases under higher dung beetle functional diversity regardless of grazing intensification

Dung removal by macrofauna such as dung beetles is an important process for nutrient cycling in pasturelands. Intensification of farming practices generally reduces species and functional diversity of terrestrial invertebrates, which may negatively affect ecosystem services. Here, we investigate the effects of cattle-grazing intensification on dung removal by dung beetles in field experiments replicated in 38 pastures around the world. Within each study site, we measured dung removal in pastures managed with low- and high-intensity regimes to assess between-regime differences in dung beetle diversity and dung removal, whilst also considering climate and regional variations. The impacts of intensification were heterogeneous, either diminishing or increasing dung beetle species richness, functional diversity, and dung removal rates. The effects of beetle diversity on dung removal were more variable across sites than within sites. Dung removal increased with species richness across sites, while functional diversity consistently enhanced dung removal within sites, independently of cattle grazing intensity or climate. Our findings indicate that, despite intensified cattle stocking rates, ecosystem services related to decomposition and nutrient cycling can be maintained when a functionally diverse dung beetle community inhabits the human-modified landscape

Global distribution patterns provide evidence of niche shift by the introduced African dung beetle Digitonthophagus gazella

The establishment of cattle ranches throughout the world has prompted the release of dung beetles as biological control agents that reduce pasture fouling and control dung‐breeding flies. One of these beetles, Digitonthophagus gazella (Fabricius) (Coleoptera: Scarabaeidae), that is native to southeast Africa, has been introduced into the Americas, Australia, and New Zealand. Distribution records for this species have been used to develop climate models of potential future establishment. Recent studies, however, identify D. gazella as a complex of seven species. Taking into account this revision, and the clear identification of the records belonging to the actual D. gazella, we developed environmental models to identify factors that have contributed to the establishment of this species across regions and habitats. We compared the environmental conditions of D. gazella in its native range against those in the regions where the species has or has not established. Our results indicate that D. gazella is still absent in certain parts of Central and South America and parts of Africa where it could potentially establish. We speculate that its distribution in Africa is limited by competitive exclusion. The introduction of D. gazella in America is relatively recent, such that the full extent of its distribution has probably yet to be realized. In Australia and North America, D. gazella is present in regions not predicted according to its native environmental conditions. This discrepancy may reflect a lack of competitive exclusion, phenotypic plasticity, and/or genetic adaptation. Our analyses suggest that the species has the ability to adapt to a wide range of environmental conditions that are extremely different from those in their native region. The species represents a useful case study to indicate that an introduced species may expand its realized niche beyond what is expected based on apparent environmental limits in the species native range.Appendix S1. Digitonthophagus gazella geographical records included in the analysis.Appendix S2. Explanatory variables deleted in the various phases of the screening analysis and those finally selected. Variance inflation factor (V): variables deleted by having a V value <5 in the geographical background (GB) of the native area of Digitonthophagus gazella. Index (I): variables deleted after applying the instability index to identify those with the highest capacity to discriminate between the environmental conditions in the presence cells against those prevailing in the GB area. F: finally selected variables.The data from New Zealand are courtesy of the Dung Beetle Release Strategy Group (DBRSG) and Landcare Research Manaaki Whenua.A Colciencias Ph.D. scholarship.https://onlinelibrary.wiley.com/journal/157074582021-08-11hj2021Zoology and Entomolog

Mapping the human genetic architecture of COVID-19

The genetic make-up of an individual contributes to the susceptibility and response to viral infection. Although environmental, clinical and social factors have a role in the chance of exposure to SARS-CoV-2 and the severity of COVID-191,2, host genetics may also be important. Identifying host-specific genetic factors may reveal biological mechanisms of therapeutic relevance and clarify causal relationships of modifiable environmental risk factors for SARS-CoV-2 infection and outcomes. We formed a global network of researchers to investigate the role of human genetics in SARS-CoV-2 infection and COVID-19 severity. Here we describe the results of three genome-wide association meta-analyses that consist of up to 49,562 patients with COVID-19 from 46 studies across 19 countries. We report 13 genome-wide significant loci that are associated with SARS-CoV-2 infection or severe manifestations of COVID-19. Several of these loci correspond to previously documented associations to lung or autoimmune and inflammatory diseases3,4,5,6,7. They also represent potentially actionable mechanisms in response to infection. Mendelian randomization analyses support a causal role for smoking and body-mass index for severe COVID-19 although not for type II diabetes. The identification of novel host genetic factors associated with COVID-19 was made possible by the community of human genetics researchers coming together to prioritize the sharing of data, results, resources and analytical frameworks. This working model of international collaboration underscores what is possible for future genetic discoveries in emerging pandemics, or indeed for any complex human disease