| Terrestrial carbon inputs to inland waters: A current synthesis of estimates and uncertainty |
47 |
| Greenhouse gas emissions from lakes and impoundments: Upscaling in the face of global change |
42 |
| Interactions between sunlight and microorganisms influence dissolved organic matter degradation along the aquatic continuum |
23 |
| Increasing dominance of terrigenous organic matter in circumpolar freshwaters due to permafrost thaw |
21 |
| Stoichiometry of carbon, nitrogen, and phosphorus through the freshwater pipe |
20 |
| Nitrogen transformations differentially affect nutrient-limited primary production in lakes of varying trophic state |
17 |
| The study of carbon in inland waters-from isolated ecosystems to players in the global carbon cycle |
15 |
| Extreme isomeric complexity of dissolved organic matter found across aquatic environments |
15 |
| Anthropogenic influences on riverine fluxes of dissolved inorganic carbon to the oceans |
15 |
| Climate warming response of mountain lakes affected by variations in snow |
13 |
| A synthesis of carbon dioxide and methane dynamics during the ice-covered period of northern lakes |
13 |
| Dissolved black carbon in aquatic ecosystems |
12 |
| Nutrient limitation constrains thermal tolerance in freshwater phytoplankton |
12 |
| Seasonal ecosystem metabolism across shallow benthic habitats measured by aquatic eddy covariance |
12 |
| Landscape process domains drive patterns of CO2 evasion from river networks |
12 |
| Beyond respiration: Controls on lateral carbon fluxes across the terrestrial-aquatic interface |
11 |
| Carbon dioxide and methane emissions of Swedish low-order streams-a national estimate and lessons learnt from more than a decade of observations |
11 |
| Consequences of lake and river ice loss on cultural ecosystem services |
9 |
| Highest plasticity of carbon-concentrating mechanisms in earliest evolved phytoplankton |
8 |
| Sediment respiration drives circulation and production of CO2 in ice-covered Alaskan arctic lakes |
8 |
| Pipes or chimneys? For carbon cycling in small boreal lakes, precipitation matters most |
8 |
| Hot tops, cold bottoms: Synergistic climate warming and shielding effects increase carbon burial in lakes |
7 |
| Carbon sink and source dynamics of a eutrophic deep lake using multiple flux observations over multiple years |
7 |
| Evidence for regional aeolian transport of freshwater micrometazoans in arid regions |
7 |
| Response of a fringing reef coastline to the direct impact of a tropical cyclone |
6 |
| Catch and release: Hyporheic retention and mineralization of N-fixing Nostoc sustains downstream microbial mat biomass in two polar desert streams |
6 |
| Hydrologic controls on pCO(2) and CO2 efflux in US streams and rivers |
6 |
| Biogeochemical tools for characterizing organic carbon in inland aquatic ecosystems |
6 |
| A geography of lake carbon cycling |
5 |
| Marine microbial community responses related to wetland carbon mobilization in the coastal zone |
5 |
| Tree-DOM: Dissolved organic matter in throughfall and stemflow |
5 |
| Copepod respiration increases by 7% per degrees C increase in temperature: A meta-analysis |
5 |
| Toward a more integrative perspective on carbon metabolism across lentic and lotic inland waters |
4 |
| Elemental content and stoichiometry of SAR11 chemoheterotrophic marine bacteria |
4 |
| Dynamic processing of DOM: Insight from exometabolomics, fluorescence spectroscopy, and mass spectrometry |
4 |
| Engineered headwaters can act as sources of dissolved organic matter and nitrogen to urban stream networks |
4 |
| Velocity-amplified microbial respiration rates in the lower Amazon River |
4 |
| Marine bacterial richness increases towards higher latitudes in the eastern Indian Ocean |
4 |
| Recovery of reef-scale calcification following a bleaching event in Kane'ohe Bay, Hawai'i |
4 |
| Wind and trophic status explain within and among-lake variability of algal biomass |
4 |
| Emergent productivity regimes of river networks |
4 |
| Particulate inorganic to organic carbon production as a predictor for coccolithophorid sensitivity to ongoing ocean acidification |
3 |
| Motility drives bacterial encounter with particles responsible for carbon export throughout the ocean |
3 |
| In the wake of a major hurricane: Differential effects on early vs. late successional seagrass species |
3 |
| Urea as a source of nitrogen to giant kelp (Macrocystis pyrifera) |
3 |
| Fluorescent organic exudates of corals and algae in tropical reefs are compositionally distinct and increase with nutrient enrichment |
3 |
| Oxygen dynamics control the burial of organic carbon in a eutrophic reservoir |
3 |
| Hydrologic setting constrains lake heterotrophy and terrestrial carbon fate |
3 |
| Vegetation transitions drive the autotrophy-heterotrophy balance in Arctic lakes |
3 |
| Phosphonate utilization by eukaryotic phytoplankton |
3 |
