268 results on '"Grossart, H-P"'
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102. Overview of a mesocosm experiment investigating the impact of phytoplankton on the microbial loop
103. Microbial dynamics in autotrophic and heterotrophic seawater mesocosms. III. Organic matter fluxes
104. Microbial dynamics in autotrophic and heterotrophic seawater mesocosms. I. Effect of phytoplankton on the microbial loop
105. Overview of a mesocosm experiment investigating the impact of phytoplankton on the microbial loop
106. Interactions between marine snow and heterotrophic bacteria: aggregate formation and microbial dynamics.
107. Testing the effect of CO2 concentration on dynamics of marine heterotrophic bacterioplankton
108. Response of <i>Nodularia spumigena</i> to <i>p</i>CO<sub>2</sub> – Part 1: Growth, production and nitrogen cycling
109. Response of Nodularia spumigena to pCO2 – Part I: Growth, production and nitrogen cycling
110. Microbe-particle interactions in the plankton: flagellate colonization and grazing on attached bacteria.
111. Bacterial dynamics on particles: Colonization, interaction and growth.
112. Particle associated flagellates: swimming patterns, colonization rates, and grazing on attached bacteria.
113. The effect of different CO2 concentrations on bacterial abundances and activity in the course of a diatom bloom
114. Hydrolysis rates of specific polysaccharides in mesocosms with high or low atmospheric CO2 concentrations
115. Pelagic Ecosystems in a High CO2 Ocean: the Mesocosm Approach
116. Microbial dynamics on marine snow: colonization, growth, detachment, and mortality of attached bacteria.
117. Bacterial Colonization of Marine Snow Particles: Growth and Inter-Specific Interactions
118. Microbial dynamics on natural diatom aggregates in Øresund, Denmark.
119. Intractable, and here's why
120. Effects of sea surface warming on the production and composition of dissolved organic matter during phytoplankton blooms: results from a mesocosm study
121. Mechanisms and rates of bacterial colonization of sinking aggregates.
122. Microbial Ecology of Organic Aggregates in Aquatic Ecosystems.
123. Flow and diffusion around suspended particles and aggregates implications for colonization, growth and predation by attached biota.
124. Microbial degradation of organic carbon and nitrogen on diatom aggregates.
125. Bacterial motility in the sea and its ecological implications
126. Coupling of heterotrophic bacteria to phytoplankton bloom development at different <i>p</i>CO<sub>2</sub> levels: a mesocosm study
127. Availability of phosphate for phytoplankton and bacteria and of glucose for bacteria at different <i>p</i>CO<sub>2</sub> levels in a mesocosm study
128. Competition for inorganic and organic forms of nitrogen and phosphorous between phytoplankton and bacteria during an <i>Emiliania huxleyi</i> spring bloom
129. Mesocosm CO2 perturbation studies: from organism to community level
130. Coupling of heterotrophic bacteria to phytoplankton bloom development at different pCO2 levels: a mesocosm study
131. Bacterial growth and respiratory carbon turnover on suspended organic aggregates.
132. Particulate Combined Amino Acids: A Key Factor of Microbial Degradation on Aggregates?
133. Bacterial Production and Growth Efficiencies: Direct Measurements on Riverine Aggregates.
134. Bacterial growth and grazing on diatom aggregates: Respiratory carbon turnover as a function of aggregate size and sinking velocity.
135. Availability of phosphate for phytoplankton and bacteria and of labile organic carbon for bacteria at different pCO2 levels in a mesocosm study
136. Competition for inorganic and organic forms of nitrogen and phosphorous between phytoplankton and bacteria during an Emiliania huxleyi spring bloom (PeECE II)
137. Effects of CO2 perturbation on phosphorus pool sizes and uptake in a mesocosm experiment during a low productive summer season in the northern Baltic Sea.
138. Photosynthesis, respiration, and carbon turnover in sinking marine snow from surface waters of Southern California Bight: Implications for the carbon cycle in the ocean.
139. Photosynthesis, respiration, and carbon turnover in marine snow in oligotrophic water.
140. Corrigendum to: The global Microcystis interactome.
141. Increasing addition of autochthonous to allochthonous carbon in nutrient-rich aquatic systems stimulates carbon consumption but does not alter bacterial community composition.
142. Response of Nodularia spumigena to pCO2 -- Part 1: Growth, production and nitrogen cycling.
143. Response of Nodularia spumigena to pCO2 -- Part I: Growth, production and nitrogen cycling.
144. Coupling of heterotrophic bacteria to phytoplankton bloom development at different pCO2 levels: a mesocosm study.
145. Availability of phosphate for phytoplankton and bacteria and of glucose for bacteria at different pCO2 levels in a mesocosm study.
146. Competition for inorganic and organic forms of nitrogen and phosphorous between phytoplankton and bacteria during an Emiliania huxleyi spring bloom.
147. Availability of phosphate for phytoplankton and bacteria and of labile organic carbon for bacteria at different pCO2 levels in a mesocosm study.
148. Dynamics of extracellular enzyme activities in seawater under changed atmospheric pCO2: a mesocosm investigation
149. Marine snow particles in the oligotrophic Sargasso Sea as analysed by amplicon sequencing: composition and linkage to the plankton
150. Methanogenic archaea associated to Microcystis sp. in field samples and in culture.
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