15 Sep 2022
| Highlight paper
Observation-constrained estimates of the global ocean carbon sink from Earth system models
Biogeosciences, 19, 4431–4457,
2022 15 Sep 2022
The influence of near-surface sediment hydrothermalism on the TEX86 tetraether-lipid-based proxy and a new correction for ocean bottom lipid overprinting
Biogeosciences, 19, 4459–4477,
2022 16 Sep 2022
Observed and projected global warming pressure on coastal hypoxia
Biogeosciences, 19, 4479–4497,
2022 16 Sep 2022
Allometric equations and wood density parameters for estimating aboveground and woody debris biomass in Cajander larch (Larix cajanderi) forests of northeast Siberia
Biogeosciences, 19, 4499–4520,
2022 19 Sep 2022
Effect of the presence of plateau pikas on the ecosystem services of alpine meadows
Biogeosciences, 19, 4521–4532,
2022 21 Sep 2022
Do bacterial viruses affect framboid-like mineral formation?
Biogeosciences, 19, 4533–4550,
2022 21 Sep 2022
High-resolution vertical biogeochemical profiles in the hyporheic zone reveal insights into microbial methane cycling
Biogeosciences, 19, 4551–4569,
2022 22 Sep 2022
Dissolved organic matter concentration and composition discontinuity at the peat–pool interface in a boreal peatland
Biogeosciences, 19, 4571–4588,
2022 27 Sep 2022
A Numerical reassessment of the Gulf of Mexico carbon system in connection with the Mississippi River and global ocean
Biogeosciences, 19, 4589–4618,
2022 28 Sep 2022
Mediterranean seagrasses as carbon sinks: methodological and regional differences
Biogeosciences, 19, 4619–4637,
2022 29 Sep 2022
Diversity and assembly processes of microbial eukaryotic communities in Fildes Peninsula Lakes (West Antarctica)
Biogeosciences, 19, 4639–4654,
2022