Effects of rising temperature on the formation and microbial degradation of marine diatom aggregates

Effects of elevated temperature on the formation and subsequent degradation of diatom aggregates were studied in a laboratory experiment with a natural plankton community from the Kiel Fjord (Baltic Sea). Aggregates were derived from diatom blooms that developed in indoor mesocosms at 2.5 and 8.5 degrees C, corresponding to the 1993 to 2002 mean winter in situ temperature of the Western Baltic Sea and the projected sea surface temperature during winter in 2100, respectively. Formation and degradation of diatom aggregates at these 2 temperatures in the dark were promoted with roller tanks over a period of 11 d. Comparison of the 2 temperature settings revealed an enhanced aggregation potential of diatom cells at elevated temperature, which was likely induced by an increased concentration of transparent exopolymer particles (TEP). The enhanced aggregation potential led to a significantly higher proportion of particulate organic matter in aggregates at 8.5 degrees C. Moreover, the elevated temperature favoured the growth of bacteria, bacterial biomass production, and the activities of sugar- and protein-degrading extracellular enzymes in aggregates. Stimulating effects of rising temperature on growth and metabolism of the bacterial community resulted in an earlier onset of aggregate degradation and silica dissolution. Remineralization of carbon in aggregates at elevated temperature was partially compensated by the formation of carbon-rich TEP during dark incubation. Hence, our results suggest that increasing temperature will affect both formation and degradation of diatom aggregates. We conclude that the vertical export of organic matter through aggregates may change in the future, depending on the magnitude and vertical depth penetration of warming in the ocean.

[1]  U. Sommer,et al.  Climate warming in winter affects the coupling between phytoplankton and bacteria during the spring bloom : a mesocosm study , 2008 .

[2]  O. Ragueneau,et al.  Evidence for reduced biogenic silica dissolution rates in diatom aggregates , 2007 .

[3]  J. Iriberri,et al.  Influence of age of aggregates and prokaryotic abundance on glucose and leucine uptake by heterotrophic marine prokaryotes. , 2007, International microbiology : the official journal of the Spanish Society for Microbiology.

[4]  H. Maske,et al.  Marine Heterotrophic Bacteria in Continuous Culture, the Bacterial Carbon Growth Efficiency, and Mineralization at Excess Substrate and Different Temperatures , 2007, Microbial Ecology.

[5]  O. Ragueneau,et al.  Si and C interactions in the world ocean: Importance of ecological processes and implications for the role of diatoms in the biological pump , 2006 .

[6]  U. Sommer,et al.  An indoor mesocosm system to study the effect of climate change on the late winter and spring succession of Baltic Sea phyto- and zooplankton , 2006, Oecologia.

[7]  C. Arnosti Speed bumps and barricades in the carbon cycle: Substrate structural effects on carbon cycling , 2004 .

[8]  U. Riebesell,et al.  Polysaccharide aggregation as a potential sink of marine dissolved organic carbon , 2004, Nature.

[9]  B. Paulsen,et al.  RELATIVE INCREASE OF DEOXY SUGARS DURING MICROBIAL DEGRADATION OF AN EXTRACELLULAR POLYSACCHARIDE RELEASED BY A TROPICAL FRESHWATER THALASSIOSIRA SP. (BACILLARIOPHYCEAE) 1 , 2003 .

[10]  H. Grossart,et al.  Microbial dynamics on diatom aggregates in Øresund, Denmark , 2003 .

[11]  A. Engel,et al.  Chemical and Biological Composition of Suspended Particles and Aggregates in the Baltic Sea in Summer (1999) , 2002 .

[12]  H. Grossart,et al.  Microbial ecology of organic aggregates in aquatic ecosystems , 2002 .

[13]  T. Kiørboe Formation and fate of marine snow: small-scale processes with large- scale implications , 2001 .

[14]  F. Azam,et al.  Bacterial control of silicon regeneration from diatom detritus: Significance of bacterial ectohydrolases and species identity , 2001 .

[15]  U. Passow,et al.  Carbon and nitrogen content of transparent exopolymer particles (TEP) in relation to their Alcian Blue adsorption , 2001 .

[16]  H. Grossart,et al.  Microbial degradation of organic carbon and nitrogen on diatom aggregates , 2001 .

[17]  W. Wiebe,et al.  Temperature and substrates as interactive limiting factors for marine heterotrophic bacteria , 2001 .

[18]  H. Grossart,et al.  Bacterial growth and grazing on diatom aggregates: Respiratory carbon turnover as a function of aggregate size and sinking velocity , 2000 .

[19]  A. Engel The role of transparent exopolymer particles (TEP) in the increase in apparent particle stickiness (α) during the decline of a diatom bloom , 2000 .

[20]  G. Herndl,et al.  Production of exopolymer particles by marine bacterioplankton under contrasting turbulence conditions , 1999 .

[21]  D. Thornton,et al.  Effect of temperature on the aggregation of Skeletonema costatum (Bacillariophyceae) and the implication for carbon flux in coastal waters , 1998 .

[22]  D. Karl,et al.  ECTOAMINOPEPTIDASE SPECIFICITY AND REGULATION IN ANTARCTIC MARINE PELAGIC MICROBIAL COMMUNITIES , 1998 .

[23]  H. Dam,et al.  Sedimentation of phytoplankton during a diatom bloom : Rates and mechanisms , 1996 .

[24]  G. Herndl,et al.  Ultrastructure of marine snow. II. Microbiological considerations , 1996 .

[25]  Alice L. Alldredge,et al.  A dye-binding assay for the spectrophotometric measurement of transparent exopolymer particles (TEP) , 1995 .

[26]  J. Rath,et al.  Characteristics and Diversity of β-d-Glucosidase (EC 3.2.1.21) Activity in Marine Snow , 1994, Applied and environmental microbiology.

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

[28]  C. Duarte,et al.  Patterns in decomposition rates among photosynthetic organisms: the importance of detritus C:N:P content , 1993, Oecologia.

[29]  Bruce E. Logan,et al.  The abundance and significance of a class of large, transparent organic particles in the ocean , 1993 .

[30]  B. Karrasch,et al.  Evidence for dependency of bacterial growth on enzymatic hydrolysis of particulate organic matter in the mesopelagic ocean , 1993 .

[31]  David C. Smith,et al.  Intense hydrolytic enzyme activity on marine aggregates and implications for rapid particle dissolution , 1992, Nature.

[32]  M. Karner,et al.  Extracellular enzymatic activity and secondary production in free-living and marine-snow-associated bacteria , 1992 .

[33]  W. Wiebe,et al.  Bacterial Growth in the Cold: Evidence for an Enhanced Substrate Requirement , 1992, Applied and environmental microbiology.

[34]  David M. Karl,et al.  VERTEX: carbon cycling in the northeast Pacific , 1987 .

[35]  M. Brzezinski,et al.  THE Si:C:N RATIO OF MARINE DIATOMS: INTERSPECIFIC VARIABILITY AND THE EFFECT OF SOME ENVIRONMENTAL VARIABLES 1 , 1985 .

[36]  A. Kamatani Dissolution rates of silica from diatoms decomposing at various temperatures , 1982 .

[37]  J. Fuhrman,et al.  Thymidine incorporation as a measure of heterotrophic bacterioplankton production in marine surface waters: Evaluation and field results , 1982 .

[38]  Thomas D. Brock,et al.  Calculating solar radiation for ecological studies , 1981 .

[39]  K. Porter,et al.  The use of DAPI for identifying and counting aquatic microflora1 , 1980 .

[40]  H. Grossart,et al.  Comparison of cell-specific activity between free-living and attached bacteria using isolates and natural assemblages. , 2007, FEMS microbiology letters.

[41]  J. Greenwood,et al.  Biogenic silica dissolution in seawater — in vitro chemical kinetics , 2001 .

[42]  W Ogana,et al.  Contribution of Working Group 1 to the Third Assessment Report of the Intergovernmental Panel on Climate Change , 2001 .

[43]  H. Ducklow,et al.  Oceanic Bacterial Production , 1992 .

[44]  U. Riebesell Particle aggregation during a diatom bloom. II. Biological aspects , 1991 .

[45]  R. Chróst Environmental Control of the Synthesis and Activity of Aquatic Microbial Ectoenzymes , 1991 .

[46]  A. Decho,et al.  Microbial exopolymer secretions in ocean environments: their role(s) in food webs and marine processes , 1990 .

[47]  G. Herndl Ecology of amorphous aggregations (marine snow) in the Northern Adriatic Sea. II. Microbial density and activity in marine snow and its implication to overall pelagic processes , 1988 .

[48]  Alice L. Alldredge,et al.  Characteristics, dynamics and significance of marine snow , 1988 .

[49]  Vernon L. Asper,et al.  Measuring the flux and sinking speed of marine snow aggregates , 1987 .

[50]  D. Caron,et al.  Production of heterotrophic bacteria inhabiting macroscopic organic aggregates (marine snow) from surface waters , 1986 .

[51]  S. Fowler,et al.  Role of large particles in the transport of elements and organic compounds through the oceanic water column , 1986 .

[52]  V. Smetácek Role of sinking in diatom life-history cycles: ecological, evolutionary and geological significance , 1985 .

[53]  H. Hoppe Significance of exoenzymatic activities in the ecology of brackish water: measurements by means of methylumbelliferyl-substrates , 1983 .

[54]  J. Strickland A practical hand-book of seawater analysis , 1972 .

[55]  T. Parsons,et al.  A practical handbook of seawater analysis , 1968 .

[56]  F. A. Richards,et al.  The influence of organisms on the composition of sea-water , 1963 .

[57]  J. Lewin The dissolution of silica from diatom walls , 1961 .