Biology subjects

Emerson, B.

Publications and source records attributed to Emerson, B..

3 recordsLinked to original sources

bioRxiv2026

Global failure to track international biodiversity targets on islands

Islands harbour exceptional biodiversity but face severe threats, making their conservation crucial to achieving the goals and targets of the Kunming-Montreal Global Biodiversity Framework. We therefore evaluated whether existing indicators can track progress toward the Framework's 23 targets across islands worldwide. We screened 504 biodiversity and socioeconomic indicators from the official framework and other global initiatives, retaining 47 indicators. Historical time series from 1950 onward were modelled and projected to 2030. Indicators were also classified using the Driver-Pressure-State-Impact-Response (DPSIR) and Theory of Change (ToC). Results showed uneven progress: eight targets improved across all available indicators, while ten displayed conflicting trends. Nearly half of the indicators focused on policy and management responses showed improvement, whereas trends in biodiversity pressures and states were mixed. Critically, 15 of 23 targets (65%) lacked a suitable headline indicator, and five targets had no indicator at all. Notably, Targets 2 and 8, addressing ecosystem restoration and climate change impacts, respectively, lacked island indicators entirely. Over half of the available indicators (29 of 47; 62%) were reported at the national level, limiting their applicability to subnational island jurisdictions and potentially obscuring differences between mainland and island conditions. Most targets also lacked quantitative objectives, limiting evaluation of whether the rate of change is sufficient to meet the targets by 2030. We recommend island-level reporting, island-specific indicators, and quantitative benchmarks tailored to island needs.

ecology↗

bioRxiv2020

The hepatic compensatory response to elevated systemic sulfide impairs medium chain fat oxidation and promotes diabetes

Impaired hepatic glucose and lipid metabolism are hallmarks of type-2 diabetes. Increased sulfide production from cysteine, or sulfide-donor compounds, may beneficially regulate hepatic metabolism. Disposal of sulfide through the sulfide oxidation pathway (SOP) is critical for maintaining sulfide within a safe physiological range. We show that mice lacking the liver-enriched mitochondrial SOP enzyme thiosulfate sulfur-transferase (Tst-/- mice) exhibit high circulating sulfide, increased gluconeogenesis, hypertriglyceridemia and fatty liver, despite whole-body insulin-sensitisation. Unexpectedly, hepatic sulfide levels were normal in Tst-/- mice, a result of homeostatic induction of mitochondrial sulfide disposal and glutathione excretion associated with net suppression of protein persulfidation and nuclear respiratory factor-2 target proteins. Proteomic and persulfidomic profiling converged on gluconeogenesis and hepatic lipid metabolism and revealed a selective deficit in medium-chain fatty acid oxidation in Tst-/- mice. We reveal a critical role for TST in hepatic metabolism that raises implications for sulfide-donor strategies in the context of liver function and metabolic disease.

physiology↗

bioRxiv2018

An integrated model of population genetics and community ecology

AimQuantifying abundance distributions is critical for understanding both how communities assemble, and how community structure varies through time and space, yet estimating abundances requires considerable investment in field work. Community-level population genetic data potentially offer a powerful way to indirectly infer richness, abundance, and the history of accumulation of biodiversity within a community. Here we introduce a joint model linking neutral community assembly and comparative phylogeography to generate both community-level richness, abundance and genetic variation under a neutral model, capturing both equilibrium and non-equilibrium dynamics.\n\nLocationGlobal.\n\nMethodsOur model combines a forward-time individual-based community assembly process with a rescaled backward-time neutral coalescent model of multi-taxa population genetics. We explore general dynamics of genetic and abundance-based summary statistics and use approximate Bayesian computation (ABC) to estimate parameters underlying the model of island community assembly. Finally, we demonstrate two applications of the model using community-scale mtDNA sequence data and densely sampled abundances of an arachnid community on La Reunion. First, we use genetic data alone to estimate a summary of the abundance distribution, ground-truthing this against the observed abundances. Then we jointly use the observed genetic data and abundances to estimate the proximity of the community to equilibrium.\n\nResultsSimulation experiments of our ABC procedure demonstrate that coupling abundance with genetic data leads to improved accuracy and precision of model parameter estimates compared with using abundance-only data. We further demonstrate reasonable precision and accuracy in estimating a metric underlying the shape of the abundance distribution, temporal progress toward local equilibrium, and several key parameters of the community assembly process. For the insular arachnid assemblage, we find the joint distribution of genetic diversity and abundance approaches equilibrium expectations, and that the Shannon entropy of the observed abundances can be estimated using genetic data alone.\n\nMain ConclusionsThe framework that we present unifies neutral community assembly and comparative phylogeography to characterize the community-level distribution of both abundance and genetic variation through time, providing a resource that should greatly enhance understanding of both the processes structuring ecological communities and the associated aggregate demographic histories.

evolutionary biology↗