Greenhouse gas emissions from two rewetted peatlands previously managed for forestry

The aim of this study was to investigate the controls on carbon dioxide (CO2), methane (CH4) and nitrous oxide (N2O) dynamics on a blanket bog (at Pollagoona) and a raised bog (at Scohaboy) in Ireland after felling of plantation forestry and rewetting, and to produce annual balances for each gas at both sites. Gas fluxes were measured during a twelve-month period using the chamber method. Microsite types reflecting the dominant plant species at the chamber plots were identified and classified as Eriophorum-Sphagnum, Cladonia-Calluna and Molinia at Pollagoona and Eriophorum-Sphagnum, Cladonia-mosses, Eriophorum and brash (logging residues) at Scohaboy. The relationships between gas fluxes and environmental variables were assessed, and regression models were used to estimate annual CO2 and CH4 gas balances for each microsite type. Annual estimates of N2O exchange were calculated using seasonal means. Over the course of the study both sites acted as CO2 and CH4 sources. Although Pollagoona was an overall net source of CO2-C (131.6 ± 298.3 g m-2 yr-1), one microsite type (Cladonia-Calluna) acted as a strong sink for CO2-C (-142.8 g m-2 yr-1). Molinia microsites exhibited the highest CH4-C emissions (2.53 ± 1.01 g m-2 yr-1). Nitrous oxide emissions at Pollagoona were calculated as 12 μg m-2 yr-1. Scohaboy acted as a large CO2-C source (585.3 ± 241.5 g m-2 yr-1) (all microsite types) despite re-vegetation of non-brash plots, due to the availability of fresh organic matter across the site. Scohaboy was also a CH4-C source, emitting 3.25 ± 0.58 g m-2 yr-1. Emissions of both CO2-C (819.31 ± 57.7 g m-2 yr-1) and CH4-C (4.76 ± 0.98 g m-2 yr-1) were highest from the brash plots. Annual N2O-N emissions were small over the study period (72 μg m-2 yr-1). Our results indicate that, despite remedial work being conducted on both peatlands to raise the water table, the C sink function has not yet been restored at either site

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function

Reduced glomerular filtration rate defines chronic kidney disease and is associated with cardiovascular and all-cause mortality. We conducted a meta-analysis of genome-wide association studies for estimated glomerular filtration rate (eGFR), combining data across 133,413 individuals with replication in up to 42,166 individuals. We identify 24 new and confirm 29 previously identified loci. Of these 53 loci, 19 associate with eGFR among individuals with diabetes. Using bioinformatics, we show that identified genes at eGFR loci are enriched for expression in kidney tissues and in pathways relevant for kidney development and transmembrane transporter activity, kidney structure, and regulation of glucose metabolism. Chromatin state mapping and DNase I hypersensitivity analyses across adult tissues demonstrate preferential mapping of associated variants to regulatory regions in kidney but not extra-renal tissues. These findings suggest that genetic determinants of eGFR are mediated largely through direct effects within the kidney and highlight important cell types and biological pathways