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Duvall, E.

Publications and source records attributed to Duvall, E..

2 recordsLinked to original sources

Anthropogenic supply of nutrients in a wildlife reserve may compromise conservation success

In nutrient-poor wildlife reserves it has become common-place to provide supplemental mineral resources for wildlife. Yet, the impacts of anthropogenic mineral supplementation on community-wide wildlife nutrition, behaviour and subsequent impact on ecosystem processes remain poorly understood. Here, we examine the contribution of anthropogenic mineral lick provision to wildlife nutrient intake across a community of large mammals (>10kg) in the southern Kalahari Desert. Based on predicted daily nutrient requirements and a faecal nutrient assessment, large herbivores appear deficient in phosphorus (P), sodium (Na) and zinc (Zn). For these nutrients, anthropogenic salt and mineral licks constitute an important (>10%) source of nutrient intake helping to reduce or overcome requirement deficits. Larger-bodied species disproportionately consumed licks (p<0.01), acquiring more nutritional benefits. A comprehensive assessment of animal body condition indicated that in general large herbivores display good health. However, bulk grazers, hindgut fermenters and females were more likely to display signs of malnourishment. We discuss how provisioning of anthropogenic mineral licks may be inflating large herbivore populations beyond the long-term carrying capacity of the reserve, with subsequent impacts for ecosystem integrity and herbivore population instability. Based on results presented here, it is clear that anthropogenic provision of mineral licks should be considered carefully by wildlife managers aiming to conserve or restore natural processes in conservation and rewilding landscapes.

ecology↗

Single-cell Transcriptome and Accessible Chromatin Dynamics During Endocrine Pancreas Development

Delineating gene regulatory networks that orchestrate cell-type specification is an ongoing challenge for developmental biology studies. Single-cell analyses offer opportunities to address these challenges and accelerate discovery of rare cell lineage relationships and mechanisms underlying hierarchical lineage decisions. Here, we describe the molecular analysis of pancreatic endocrine cell differentiation using single-cell gene expression, chromatin accessibility assays coupled to genetic labeling and cell sorting. We uncover transcription factor networks that delineate {beta}-, - and{delta} -cell lineages. Through genomic footprint analysis we identify transcription factor-regulatory DNA interactions governing pancreatic cell development at unprecedented resolution. Our analysis suggests that the transcription factor Neurog3 may act as a pioneer transcription factor to specify the pancreatic endocrine lineage. These findings could improve protocols to generate replacement endocrine cells from renewable sources, like stem cells, for diabetes therapy.

developmental biology↗