Description: Aggregation of algae, mainly diatoms, is an important process in marine systems leading to the settling of particulate organic carbon predominantly in the form of marine snow. Exudation products of phytoplankton form transparent exopolymer particles (TEP), which acts as the glue for particle aggregation. Heterotrophic bacteria interacting with phytoplankton may influence TEP formation and phytoplankton aggregation. This bacterial impact has not been explored in detail. We hypothesized that bacteria attaching to Thalassiosira weissflogii might interact in a yet-to-be determined manner, which could impact TEP formation and aggregate abundance. The role of individual T. weissflogii-attaching and free-living new bacterial isolates for TEP production and diatom aggregation was investigated in vitro. T. weissflogii did not aggregate in axenic culture, and striking differences in aggregation dynamics and TEP abundance were observed when diatom cultures were inoculated with either diatom-attaching or free-living bacteria. The data indicated that free-living bacteria might not influence aggregation whereas bacteria attaching to diatom cells may increase aggregate formation. Interestingly, photosynthetically inactivated T. weissflogii cells did not aggregate regardless of the presence of bacteria. Comparison of aggregate formation, TEP production, aggregate sinking velocity and solid hydrated density revealed remarkable differences. Both, photosynthetically active T. weissflogii and specific diatom-attaching bacteria were required for aggregation. It was concluded that interactions between heterotrophic bacteria and diatoms increased aggregate formation and particle sinking and thus may enhance the efficiency of the biological pump.

Description: Carbon uptake and partitioning of two globally abundant diatom species, Thalassiosira weissflogii and Dactyliosolen fragilissimus, was investigated in batch culture experiments under four conditions: ambient (15°C, 400 µatm), high CO2 (15°C, 1000 µatm), high temperature (20°C, 400 µatm), and combined (20°C, 1000 µatm). The experiments were run from exponential growth into the stationary phase (six days after nitrogen depletion), allowing us to track biogeochemical dynamics analogous to bloom situations in the ocean. Elevated CO2 had a fertilizing effect and enhanced uptake of dissolved inorganic carbon (DIC) by about 8% for T. weissflogii and by up to 39% for D. fragilissimus. This was also reflected in higher cell numbers, build-up of particulate and dissolved organic matter, and transparent exopolymer particles. The CO2 effects were most prominent in the stationary phase when nitrogen was depleted and CO2(aq) concentrations were low. This indicates that diatoms in the high CO2 treatments could take up more DIC until CO2 concentrations in seawater became so low that carbon limitation occurs. These results suggest that, contrary to common assumptions, diatoms could be highly sensitive to ongoing changes in oceanic carbonate chemistry, particularly under nutrient limitation. Warming from 15 to 20 °C had a stimulating effect on one species but acted as a stressor on the other species, highlighting the importance of species-specific physiological optima and temperature ranges in the response to ocean warming. Overall, these sensitivities to CO2 and temperature could have profound impacts on diatoms blooms and the biological pump.

Description: As part of the PeECE II mesocosm project, we investigated the effects of pCO2 levels on the initial step of heterotrophic carbon cycling in the surface ocean. The activities of microbial extracellular enzymes hydrolyzing 4 polysaccharides were measured during the development of a natural phytoplankton bloom under pCO2 conditions representing glacial (190 µatm) and future (750 µatm) atmospheric pCO2. We observed that (1) chondroitin hydrolysis was variable throughout the pre-, early- and late-bloom phases, (2) fucoidanase activity was measurable only in the glacial mesocosm as the bloom developed, (3) laminarinase activity was low and constant, and (4) xylanase activity declined as the bloom progressed. Concurrent measurements of microbial community composition, using denaturing-gradient gel electrophoresis (DGGE), showed that the 2 mesocosms diverged temporally, and from one another, especially in the late-bloom phase. Enzyme activities correlated with bloom phase and pCO2, suggesting functional as well as compositional changes in microbial communities in the different pCO2 environments. These changes, however, may be a response to temporal changes in the development of phytoplankton communities that differed with the pCO2 environment. We hypothesize that the phytoplankton communities produced dissolved organic carbon (DOC) differing in composition, a hypothesis supported by changing amino acid composition of the DOC, and that enzyme activities responded to changes in substrates. Enzyme activities observed under different pCO2 conditions likely reflect both genetic and population-level responses to changes occurring among multiple components of the microbial loop.

Description: Shifts in phytoplankton composition and productivity are anticipated in the future, because phytoplankton are frequently bottom-up controlled, and environmental conditions, like temperature, partial pressure of CO2 (pCO2), and light climate continue to change. Culture experiments revealed that whereas future (elevated) pCO2 had no effect on T. weissflogii in the absence of environmental stressors, growth rate was drastically decreased under future pCO2 if cells grew under light and temperature stress. The reduction in growth rates and a smaller decline in cellular photosynthesis under high pCO2 were associated with 2- to 3-fold increases in the production of transparent exopolymer particles (TEP), in the cell quotas of organic carbon, and the chl a:C ratios. Results suggest that under light- and temperature-stressed growth, elevated pCO2 led to increased energy requirements, which were fulfilled by increased light harvesting capabilities that permitted photosynthesis of acclimatized cells to remain relatively high. This was combined with the inability of these cells to acclimatize their growth rate to sub-optimal temperatures. As a consequence, growth rate was low and decoupled from photosynthesis. This decoupling led to large cell sizes and high excretion rates in future pCO2 treatments compared to ambient treatments if growth temperature and light were sub-optimal. Under optimal growth conditions the increased energy demands required to re-equilibrate the disturbed acid-base balance in future pCO2 treatments were likely mediated by a variety of physiological acclimatization mechanisms, individually too small to show a statistically detectable response in terms of growth rate, photosynthesis, pigment concentration, or excretion.

Description: Here we present concentrations of chlorophyll a, phaeopigments, particulate organic carbon and nitrogen from water samples collected at discrete depths with a CTD-rosette during the European Iron Fertilization Experiment (EIFEX). The experiment was carried out from February 11 to March 20, 2004 in the 60-km diameter, rotating core of an eddy, formed by a meander of the Antarctic Polar Front (centred at around 49°10' S and 2°10' E). Samples were taken within the eddy inside and outside the fertilized patch, and in a few cases outside the eddy.Chlorophyll concentrations were determined by fluorometry using a Turner Design Model 10-AU digital fluorometer. Sampling, measurements and calibration of the fluorometer was carried out following the JGOFS protocol procedure (Knap et al, 1996). Results of the fluorometer calibration diverged by 5% between beginning and end of the cruise. Chlorophyll a content was calculated using average parameter values from the two calibrations. Measurement uncertainty was estimated from triplicate water samples taken from depths ranging between 10 and 100 m depth and averaged 5% of measured values. Samples for particulate organic carbon and nitrogen (POC and PON) were filtered onto precombusted Whatman GF/F filters and processed following recommendations by Lorrain et al. (2003). Samples were measured independently on three different analysers: a CN2500 CHN Analyser (Thermo Finnigan MAT) coupled to a Delta+ mass spectrometer (Thermo Finnigan MAT) via Conflo II interface (Thermo Finnigan MAT), a Carlo-Erba NA-1500 Series II elemental analyzer coupled to a Finnegan Delta+ mass spectrometer and a Euro EA Elemental Analyser. Differences due to methods were within the range of measurement variability (below 2%). The particulate organic phosphorus (POP) content was determined colorimetrically using the method from Hansen and Koroleff (1999; measurement variability 4%). Biogenic silica (BSi) was measured following the wet alkaline digestion method according to Müller and Schneider (1993; measurement variability 2%).