Evidence for grazing-mediated production of dissolved surface-active material by marine protists

Abstract Surface-active organic compounds or surfactants play important roles in a variety of upper ocean processes, including surface microlayer physics and gas exchange and the aggregation of colloidal material. Although surfactants are presumed to be produced primarily by phytoplankton, production by protozoan grazers has not been investigated. In general, the processes controlling surfactant abundance in the field are poorly understood. In this study, a two-phase laboratory system containing protists and prey was used to examine the possibility of surfactant production during protozoan grazing. Three protist species were examined, a scuticociliate, Uronema sp. (10–15 μm), and two flagellates, Cafeteria sp. (2–4 μm), and Paraphysomonas imperforata (4–8 μm). For all experimental cultures, protozoan inocula were added to rinsed bacterial suspensions ( Halomonas halodurans ) in sterile seawater. Surfactants, dissolved organic carbon (DOC) and population dynamics were monitored until protists had reached stationary growth. Surfactant activities increased during protozoan exponential growth. Surfactant production in the ciliate cultures was significantly higher than in either of the flagellate cultures. Bacterial controls maintained low DOC concentrations and surfactant activities. Estimates of protozoan surfactant production rates range from 10 −8 to 10 −9 mg protist −1 h −1 (Triton X-100 equivalents). Under non-bloom conditions (10 3 protozoan cells ml −1 ), we estimated a surfactant production rate of 10 −5 –10 −6 mg h −1 (within 1 ml of seawater), which is comparable to estimates of phytoplankton production of surface-active material during blooms. Thus, protozoan grazers constitute a potentially significant source of surface-active material in areas where protists are abundant, such as the sediment–water interface and microbial loop-dominated oligotrophic regimes.

[1]  J. Moffett,et al.  Remineralization and recycling of iron, thorium and organic carbon by heterotrophic marine protists in culture , 2001 .

[2]  B. Frost EFFECTS OF SIZE AND CONCENTRATION OF FOOD PARTICLES ON THE FEEDING BEHAVIOR OF THE MARINE PLANKTONIC COPEPOD CALANUS PACIFICUS1 , 1972 .

[3]  J. Shine,et al.  The formation of surface-active organic complexes of copper in coastal marine waters , 1995 .

[4]  Agneta Andersson,et al.  Potential importance of protozoan grazing on the accumulation of polychlorinated biphenyls (PCBs) in the pelagic food web , 1997, Hydrobiologia.

[5]  P. Liss,et al.  Polarographic measurement of surface-active material in natural waters , 1981 .

[6]  B. Gašparović,et al.  Electrochemical estimation of the dominant type of surface active substances in seawater samples using o-nitrophenol as a probe , 1994 .

[7]  V. Z̆utić,et al.  Surfactant production by marine phytoplankton , 1981 .

[8]  H. Dam,et al.  The role of surface-active carbohydrates in the flocculation of a diatom bloom in a mesocosm , 1995 .

[9]  D. Kirchman,et al.  Filtration-induced release of dissolved free amino acids: application to cultures of marine protozoa , 1990 .

[10]  J. Moffett,et al.  Dissolution of iron oxides by phagotrophic protists : Using a novel method to quantify reaction rates , 1998 .

[11]  E. Sherr,et al.  Bacterivory and herbivory: Key roles of phagotrophic protists in pelagic food webs , 1994, Microbial Ecology.

[12]  E. Kujawinski The effect of protozoan grazers on the cycling of polychlorinated biphenyls (PCBs) in marine systems , 2000 .

[13]  M. Perry,et al.  Closing the microbial loop: dissolved carbon pathway to heterotrophic bacteria from incomplete ingestion, digestion and absorption in animals , 1989 .

[14]  B. Ćosović,et al.  Adsorption behaviour of the hydrophobic fraction of organic matter in natural waters , 1989 .

[15]  F. Rassoulzadegan,et al.  Particulate and Dissolved Organic Carbon Production by the Heterotrophic Nanoflagellate Pteridomonas danica Patterson and Fenchel , 1999, Microbial Ecology.

[16]  D. Caron,et al.  Grazing and utilization of chroococcoid cyanobacteria and heterotrophic bacteria by protozoa in laboratory cultures and a coastal plankton community. , 1991 .

[17]  E. Delong,et al.  Application of rRNA-based probes for observing marine nanoplanktonic protists , 1993, Applied and environmental microbiology.

[18]  J. Iriberri,et al.  Influence of bacterial density and water temperature on the grazing activity of two freshwater ciliates , 1995 .

[19]  E. Peltzer,et al.  Some practical aspects of measuring DOC — sampling artifacts and analytical problems with marine samples , 1993 .

[20]  B. Ćosović,et al.  Fractionation of surface active substances on the XAD-8 resin: Adriatic Sea samples and phytoplankton culture media , 1996 .

[21]  L. Tranvik Colloidal and Dissolved Organic Matter Excreted by a Mixotrophic Flagellate during Bacterivory and Autotrophy , 1994, Applied and environmental microbiology.

[22]  H. Sakugawa,et al.  Isolation and chemical characterization of dissolved and particulate polysaccharides in Mikawa Bay , 1985 .

[23]  T. Nagata Release of macromolecular organic complexes by heterotrophic marine flagellates , 1992 .

[24]  J. Heinbokel Studies on the functional role of tintinnids in the Southern California Bight. I. Grazing and growth rates in laboratory cultures , 1978 .

[25]  J. G. Field,et al.  The Ecological Role of Water-Column Microbes in the Sea* , 1983 .

[26]  Bruce E. Logan,et al.  The role of particulate carbohydrate exudates in the flocculation of diatom blooms , 1994 .

[27]  U. Passow,et al.  The role of surface‐active carbohydrates in the formation of transparent exopolymer particles by bubble adsorption of seawater , 1998 .

[28]  L. Pomeroy The Ocean's Food Web, A Changing Paradigm , 1974 .

[29]  J. Moffett,et al.  Laboratory and field studies of colloidal iron oxide dissolution as mediated by phagotrophy and photolysis , 2000 .

[30]  E. Sherr,et al.  Role of microbes in pelagic food webs: a revised concept , 1988 .

[31]  T. Pleše,et al.  Determination of surfactant activity and anionic detergents in seawater and sea surface microlayer in the Mediterranean , 1985 .

[32]  D. Kirchman,et al.  Protection of protein from bacterial degradation by submicron particles , 1999 .

[33]  D. Scavia On the role of bacteria in secondary production , 1988 .

[34]  R. Iturriaga,et al.  Interactions of bactivorous grazers and heterotrophic bacteria with dissolved organic matter , 1985 .

[35]  J. C. Goldman,et al.  Impact of phytoplankton-generated surfactants on air-sea gas exchange , 1990 .