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Inputs of terrestrially derived dissolved organic matter (DOM) are increasing in alpine lakes due to multiple drivers such as climate change, tree line advancement, and insect epidemics. A 21 d micro...
We examined the role of physical dispersal in regulating patterns of diversity of marine phytoplankton in the context of global ocean simulations at eddy-permitting and coarse resolutions. Swifter cu...
Dissolved nitrogen (N) as urea ([NH2 ]2CO), nitrate (NO{ 3 ), and ammonium (NHz 4 ) was added to naturally phosphorus (P)-rich lake water (up to 175 mg P L21 ) to test the hypotheses that pollu...
In the high-nutrient, low-chlorophyll waters of the Gulf of Alaska, microcosm manipulation experiments were used to assess the effect of CO2 on growth and primary production under iron-limited and iro...
A cross-ecosystem comparison of data obtained from 92 coastal zone ecosystems worldwide revealed a strong positive response of marine phytoplankton biomass to nutrient enrichment that is highly consi...
A set of eight large (20 m3 ) mesocosms were moored in Johnson’s Dock (62839.5769S, 60822.4089W, Livingston Island, Antarctica) to experimentally generate a gradient of phytoplankton biomass and pro...
Phytoplankton growth and stoichiometry depend on the availability of multiple nutrients. We use a mathematical model of phytoplankton with flexible stoichiometry to explain patterns of phytopla...
Measurements of the phytoplankton absorption coefficient, aph (l), at the Bermuda Atlantic Times-series Study (BATS) site demonstrated a seasonal pattern of absorption in the ultraviolet (UV) ...
In oligotrophic lakes and oceans, the deep chlorophyll maximum may form independently of a maximum of phytoplankton biomass, because the ratio of chlorophyll to phytoplankton biomass (in units of car...
Freshwater dinoflagellates may form dense blooms during winter in ice-covered lakes. Unlike their marine counterparts, freshwater dinoflagellates are rarely considered to be potential toxi...

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