Bettina Reitner

Role of ultraviolet-B radiation on bacterioplankton and the availability of dissolved organic matter

Attenuation of ultraviolet (UV)-radiation into the water column is highly correlated with the concentration of the dissolved organic matter (DOM). Thus UV penetrates deeper into marine waters than into freshwater systems. DOM is efficiently cleaved by solar surface radiation levels consuming more oxygen than bacterial metabolism. This photolytically cleaved DOM exhibits higher absorbance ratios (250/365 nm) than untreated DOM. Natural bacterioplankton reach higher abundance if inoculated in previously solar-exposed DOM than in untreated DOM; during bacterial growth the absorbance ratio declines steadily indicating the utilization of the photolytically cleaved DOM. On the other hand, bacterioplankton are greatly reduced in their activity if exposed to surface solar radiation levels. Photoenzymatic repair of DNA induced by UV-A radiation, however, leads to an efficient recovery of bacterial activity once the UV-B stress is released. Turbulent mixing of the upper layers of the water column leads to a continuous alteration of the UV exposure regime. Close to the surface, bacteria and DOM are exposed to high levels of UV-B leading to a reduction in bacterial activity and to photolysis of DOM. Once mixed into deeper layers where UV-B is attenuated, but sufficient UV-A is remaining to allow photoenzymatic repair, the photolytically cleaved DOM is efficiently taken up by bacterioplankton leading to even higher bacterial activity than prior to the exposure. Thus, the overall effect of UV on bacterioplankton is actually an enhancement of bacterial activity despite their lack of protective pigments.

Rapid Growth of Planktonic Vibrio cholerae Non-O1/Non-O139 Strains in a Large Alkaline Lake in Austria: Dependence on Temperature and Dissolved Organic Carbon Quality

ABSTRACT Vibrio cholerae non-O1/non-O139 strains have caused several cases of ear, wound, and blood infections, including one lethal case of septicemia in Austria, during recent years. All of these cases had a history of local recreational activities in the large eastern Austrian lake Neusiedler See. Thus, a monitoring program was started to investigate the prevalence of V. cholerae strains in the lake over several years. Genetic analyses of isolated strains revealed the presence of a variety of pathogenic genes, but in no case did we detect the cholera toxin gene or the toxin-coregulated pilus gene, both of which are prerequisites for the pathogen to be able to cause cholera. In addition, experiments were performed to elucidate the preferred ecological niche of this pathogen. As size filtration experiments indicated and laboratory microcosms showed, endemic V. cholerae could rapidly grow in a free-living state in natural lake water at growth rates similar to those of the bulk natural bacterial population. Temperature and the quality of dissolved organic carbon had a highly significant influence on V. cholerae growth. Specific growth rates, growth yield, and enzyme activity decreased markedly with increasing concentrations of high-molecular-weight substances, indicating that the humic substances originating from the extensive reed belt in the lake can inhibit V. cholerae growth.

Microbial activity under the ice cover of the shallow Neusiedler See (Austria, Central Europe)

In an attempt to assess bacterioplankton production and growth yieldunder low temperature conditions and to compare bacterioplankton withphytoplankton production in the ice-covered water column of the shallowNeusiedler See, outdoor measurements under near in situ conditions wereperformed during the winter of 1995/96. During the investigation period,mean chlorophyll (Chl) a concentration was 21.03 ± 14.95 µg Chla l-1. Phytoplankton primary production integrated over thewater column ranged from 1.35 to production integrated over the water columnranged from 1.35 to 4.23 mg C m-2 d-1 (mean± SD = 2.46 ± 1.06 mg C m-2d-1). Bacterial abundance varied from 20 to 40×105 ml-1 for most of the investigationperiod and increased by the end of March concomitantly with the increase intemperature from 1.3 to 6.3 °C within 5 days. Mean bacterial productionwas 15.3 ± 12.8 µg C l-1 d-1(range: 3.0 to 41.7 µg C l-1 d-1) and meanbacterial growth rate 0.23 ± 0.16 d-1 following closelythe pattern in bacterial production. DOC concentration declined linearlyfrom 20.7 mg C l-1 to 16.45 mg C l-1 over the 4months period of ice cover. The contribution of humic substances to thetotal DOC pool declined from 43.6% at the end of November to37.3% at the end of March. Calculated on an area basis, phytoplanktonproduction amounted to only 16% of bacterial production which makesit unlikely that phytoplankton supply substrate for bacterioplankton growthin significant quantities when the lake is ice covered. From the observeddecline in DOC over the investigation period and assuming only negligibleinput of DOC from other sources we calculated an average DOC uptake by thebacterioplankton community of 47.5 µg C l-1d-1 resulting in a bacterial growth efficiency of 15.9%for the ice covered conditions. Based on the growth efficiency we estimatethat pelagic primary production amounts to 2.8% of the bacterialcarbon demand. This might indicate that the bacterioplankton in NeusiedlerSee sustain their high growth rates at low temperatures (<2°C formost of the investigation period) by using probably the DOC originating fromthe previous season. This DOM stems most likely from the decay of the reedPhragmites australis and its epiphytes and, probably of minor importance,from phytoplankton leachates.