The application of a plug-flow reactor to measure the biodegradable dissolved organic carbon (BDOC) in seawater.

Most of the ambient dissolved organic carbon (DOC) is refractory to microbial degradation; bacteria can consume a minor but variable part of the DOC pool over periods of hours and days. It is important to increase our knowledge of the dynamics of the biodegradable fraction of DOC (BDOC) to understand the global carbon budget. Several methods for determining BDOC have been developed; however, the problem of most of them is the time (days/weeks) required for the colonization and/or determination. In this paper, we describe the application to seawater of a plug-flow bioreactor to measure BDOC within 3-4 h. The bioreactor was built following Søndergaard and Worm [Søndergaard, M., Worm, J., 2001. Measurement of biodegradable dissolved organic carbon (BDOC) in lake water with a bioreactor. Water Res. 35, 2505-2513.] protocols for the measurement of BDOC in lake water. We analyzed BDOC on samples collected in the Gulf of Trieste during autumn-winter and summer 2003-2004. BDOC concentrations varied from 8 to 24 microM and represented from 10.3% to 25.5% of the total DOC. To evaluate the effectiveness of this method, we compared bioreactor BDOC measurement with data obtained from batch cultures. The results indicate that BDOC in coastal seawater can be measured rapidly and reliably with this bioreactor.

Organic-matter degradative potential of Halomonas glaciei isolated from frazil ice in the Ross Sea (Antarctica).

Halomonas glaciei isolated from frazil ice in the Ross Sea (Antarctica) during austral summer 2003 was phenotypically characterized and its capability of degrading organic matter was tested. We evaluated specific bacterial growth rates (mu) to understand at which temperatures bacterial growth shows a linear and direct relationship with the available substrate (4-22 degrees C) and afterwards we tested H. glaciei growth curves and degradative potential at 0, 10 and 37 degrees C using two different media (one enriched and one depleted in PO(4)). The strain grew exponentially only at 10 degrees C. The fastest hydrolysis rates were expressed by enzymes aimed at polysaccharide degradation (alpha-D-glucosidase, beta-D-glucosidase and beta-D-galactosidase) while alkaline phosphatase and aminopeptidase activities were rather low. Our data suggest a preferential demand for carbon derived from carbohydrates rather than from proteins: ectoenzyme activities transformed into carbon mobilization from organic polymers, showed that the total carbon potentially released from polysaccharides can be almost one order of magnitude higher than the protein carbon mobilization. Principal component analysis of the enzyme affinity separated the six experimental conditions, highlighting how different physical (temperature) and chemical (PO(4) enrichment or depletion) features actively lead to a differentiation in the efficiency of the ectoenzymes produced, resulting in preferential degradation of diverse kinds of organic substrates.

Delayed fluorescence as a measure of nutrient limitation in Dunaliella tertiolecta.

The applicability of the delayed fluorescence (DF) for the purpose of distinguishing the cells growing in different nutrient conditions was researched on the marine unicellular algae Dunaliella tertiolecta Butcher (Chlorophyta). The DF intensity (DFI), as a measure of living algal biomass, was compared with other biomass measures--the cell concentration, chlorophyll a and fluorescence. The photosynthetic activity index (PhAI), a non-dimensional physiological index of photosynthesis calculated from a combination of DFI and F(0) was introduced. The nitrogen deprivation was indicated by more than 50% drop of PhAI. DF decay kinetics was measured with two different illuminations (<600 nm and >650 nm). The measured curves were divided and the resulting peak utilized for the differentiation among nutrient conditions. DF decay kinetics of D. tertiolecta differed among the cells growing in various nutrient conditions, indicating changes in the photosynthesis physiology.