| Beyond clay: towards an improved set of variables for predicting soil organic matter content |
61 |
| Calcium-mediated stabilisation of soil organic carbon |
60 |
| Multiple models and experiments underscore large uncertainty in soil carbon dynamics |
30 |
| Minerals in the rhizosphere: overlooked mediators of soil nitrogen availability to plants and microbes |
25 |
| Two decades of tropical cyclone impacts on North Carolina's estuarine carbon, nutrient and phytoplankton dynamics: implications for biogeochemical cycling and water quality in a stormier world |
24 |
| The Millennial model: in search of measurable pools and transformations for modeling soil carbon in the new century |
23 |
| The impact of flooding on aquatic ecosystem services |
19 |
| Nitrogen oligotrophication in northern hardwood forests |
17 |
| Long-term nitrogen addition suppresses microbial degradation, enhances soil carbon storage, and alters the molecular composition of soil organic matter |
16 |
| River network saturation concept: factors influencing the balance of biogeochemical supply and demand of river networks |
14 |
| Dinitrogen emissions: an overlooked key component of the N balance of montane grasslands |
13 |
| The effect of a freeze-thaw cycle on dissolved nitrogen dynamics and its relation to dissolved organic matter and soil microbial biomass in the soil of a northern hardwood forest |
12 |
| Soil C:N:P stoichiometry responds to vegetation change from grassland to woodland |
12 |
| Growing season warming and winter freeze-thaw cycles reduce root nitrogen uptake capacity and increase soil solution nitrogen in a northern forest ecosystem |
12 |
| Rapid warming and salinity changes in the Gulf of Maine alter surface ocean carbonate parameters and hide ocean acidification |
12 |
| Watershed chemical cocktails': forming novel elemental combinations in Anthropocene fresh waters |
11 |
| Groundwater nitrate removal in riparian buffer zones: a review of research progress in the past 20 years |
10 |
| Soil carbon dioxide and methane fluxes from forests and other land use types in an African tropical montane region |
10 |
| Order from disorder: do soil organic matter composition and turnover co-vary with iron phase crystallinity? |
10 |
| Microbial and plant-derived compounds both contribute to persistent soil organic carbon in temperate soils |
10 |
| Faster redox fluctuations can lead to higher iron reduction rates in humid forest soils |
9 |
| River beads as a conceptual framework for building carbon storage and resilience to extreme climate events into river management |
9 |
| Methane oxidation kinetics in northern freshwater lakes |
9 |
| Three years of soil respiration in a mature eucalypt woodland exposed to atmospheric CO2 enrichment |
9 |
| DOM composition alters ecosystem function during microbial processing of isolated sources |
9 |
| Wetland flux controls: how does interacting water table levels and temperature influence carbon dioxide and methane fluxes in northern Wisconsin? |
9 |
| Factors controlling dissimilatory nitrate reduction processes in constructed stormwater urban wetlands |
9 |
| Multi-scale temporal variation of methane flux and its controls in a subtropical tidal salt marsh in eastern China |
9 |
| Improving understanding of soil organic matter dynamics by triangulating theories, measurements, and models |
9 |
| Spatial variability of organic matter properties determines methane fluxes in a tropical forested peatland |
8 |
| Homogenization of dissolved organic matter within a river network occurs in the smallest headwaters |
8 |
| Incorporation of shoot versus root-derived C-13 and N-15 into mineral-associated organic matter fractions: results of a soil slurry incubation with dual-labelled plant material |
8 |
| The sources and distribution of carbon (DOC, POC, DIC) in a mangrove dominated estuary (French Guiana, South America) |
8 |
| Episodic salinization and freshwater salinization syndrome mobilize base cations, carbon, and nutrients to streams across urban regions |
8 |
| Restored floodplains enhance denitrification compared to naturalized floodplains in agricultural streams |
7 |
| Freeze-thaw processes and intense rainfall: the one-two punch for high sediment and nutrient loads from mid-Atlantic watersheds |
7 |
| Salinity effects on greenhouse gas emissions from wetland soils are contingent upon hydrologic setting: a microcosm experiment |
7 |
| Silicon in tropical forests: large variation across soils and leaves suggests ecological significance |
7 |
| Denitrification under lake ice |
7 |
| Methane fluxes from tree stems and soils along a habitat gradient |
7 |
| Evaluating soil microbial carbon use efficiency explicitly as a function of cellular processes: implications for measurements and models |
7 |
| Shining light on the storm: in-stream optics reveal hysteresis of dissolved organic matter character |
7 |
| Interactive effects of land-use change and topography on asymbiotic nitrogen fixation in the Brazilian Atlantic Forest |
7 |
| Climate change may alter mercury fluxes in northern hardwood forests |
6 |
| Carbon biogeochemistry of a flooded Pantanal forest over three annual flood cycles |
6 |
| Aluminum effects on marine phytoplankton: implications for a revised Iron Hypothesis (Iron-Aluminum Hypothesis) |
6 |
| Historical soil drainage mediates the response of soil greenhouse gas emissions to intense precipitation events |
6 |
| Denitrification in a meromictic lake and its relevance to nitrogen flows within a moderately impacted forested catchment |
6 |
| Stable calcium isotope speciation and calcium oxalate production within beech tree (Fagus sylvatica L.) organs |
6 |
| Differential effects of chronic and acute simulated seawater intrusion on tidal freshwater marsh carbon cycling |
6 |
