Degree of oligotrophy controls the response of microbial plankton to Saharan dust

To determine the effects of Saharan dust on the abundance, biomass, community structure, and metabolic activity of oceanic microbial plankton, we conducted eight bioassay experiments between ca. 30°N and 30°S in the central Atlantic Ocean. We found that, although bulk abundance and biomass tended to remain unchanged, different groups of phytoplankton and bacterioplankton responded differently to Saharan dust addition. The predominant type of metabolic response depended on the ecosystem's degree of oligotrophy and was modulated by competition for nutrients between phytoplankton and heterotrophic bacteria. The relative increase in bacterial production, which was the dominant response to dust addition in ultraoligotrophic environments, became larger with increasing oligotrophy. In contrast, primary production, which was stimulated only in the least oligotrophic waters, became less responsive to dust as the ecosystem's degree of oligotrophy increased. Given the divergent consequences of a predominantly bacterial vs. phytoplanktonic response, dust inputs can, depending on the ecosystem's degree of oligotrophy, stimulate or weaken biological CO2 drawdown. Thus, the biogeochemical implications of changing dust fluxes might not be universal, but variable through both space and time.

[1]  J. Neff,et al.  The contemporary physical and chemical flux of aeolian dust: A synthesis of direct measurements of dust deposition , 2009 .

[2]  Sandra Martínez-García,et al.  In vivo electron transport system activity: a method to estimate respiration in natural marine microbial planktonic communities , 2009 .

[3]  E. Casamayor,et al.  Effect of Saharan dust inputs on bacterial activity and community composition in Mediterranean lakes and reservoirs , 2009 .

[4]  N. Mahowald,et al.  Toxicity of atmospheric aerosols on marine phytoplankton , 2009, Proceedings of the National Academy of Sciences.

[5]  X. Morán,et al.  Empirical Leucine-to-Carbon Conversion Factors for Estimating Heterotrophic Bacterial Production: Seasonality and Predictability in a Temperate Coastal Ecosystem , 2009, Applied and Environmental Microbiology.

[6]  Adina Paytan,et al.  Atmospheric iron deposition: global distribution, variability, and human perturbations. , 2009, Annual review of marine science.

[7]  G. Tarran,et al.  Nutrient limitation of picophytoplankton photosynthesis and growth in the tropical North Atlantic , 2008 .

[8]  J. Gasol,et al.  Linkages between bacterioplankton community composition, heterotrophic carbon cycling and environmental conditions in a highly dynamic coastal ecosystem. , 2008, Environmental microbiology.

[9]  E. Achterberg,et al.  Nitrogen and phosphorus co‐limitation of bacterial productivity and growth in the oligotrophic subtropical North Atlantic , 2008 .

[10]  E. Pulido-Villena,et al.  Bacterial response to dust pulses in the western Mediterranean: Implications for carbon cycling in the oligotrophic ocean , 2008 .

[11]  Melanie Abecassis,et al.  Ocean's least productive waters are expanding , 2008 .

[12]  E. Achterberg,et al.  Relative influence of nitrogen and phosphorous availability on phytoplankton physiology and productivity in the oligotrophic sub‐tropical North Atlantic Ocean , 2008 .

[13]  J. Gasol,et al.  Effects of resource availability and bacterivory on leucine incorporation in different groups of freshwater bacterioplankton, assessed using microautoradiography , 2006 .

[14]  Beatriz Mouriño-Carballido,et al.  Mesoscale variability in the metabolic balance of the Sargasso Sea , 2006 .

[15]  X. Morán,et al.  Seasonal dynamics of picoplankton in shelf waters of the southern Bay of Biscay , 2006 .

[16]  N. Mahowald,et al.  Atmospheric global dust cycle and iron inputs to the ocean , 2005 .

[17]  S. Bonnet,et al.  Effect of atmospheric nutrients on the autotrophic communities in a low nutrient, low chlorophyll system , 2005 .

[18]  F. Rassoulzadegan,et al.  Response of East Mediterranean surface water to Saharan dust: On-board microcosm experiment and field observations , 2005 .

[19]  M. Moran,et al.  Overview of the Marine Roseobacter Lineage , 2005, Applied and Environmental Microbiology.

[20]  S Psarra,et al.  Nature of Phosphorus Limitation in the Ultraoligotrophic Eastern Mediterranean , 2005, Science.

[21]  N. Mahowald,et al.  Global Iron Connections Between Desert Dust, Ocean Biogeochemistry, and Climate , 2005, Science.

[22]  R. Malmstrom,et al.  Contribution of SAR11 Bacteria to Dissolved Dimethylsulfoniopropionate and Amino Acid Uptake in the North Atlantic Ocean , 2004, Applied and Environmental Microbiology.

[23]  Matthew M. Mills,et al.  Iron and phosphorus co-limit nitrogen fixation in the eastern tropical North Atlantic , 2004, Nature.

[24]  Michael R. Landry,et al.  Phytoplankton growth, microzooplankton grazing, and carbon cycling in marine systems , 2004 .

[25]  M. Behrenfeld,et al.  High variability of primary production in oligotrophic waters of the Atlantic Ocean : uncoupling from phytoplankton biomass and size structure , 2003 .

[26]  William A. Siebold,et al.  SAR11 clade dominates ocean surface bacterioplankton communities , 2002, Nature.

[27]  Russ E. Davis,et al.  Robotic Observations of Dust Storm Enhancement of Carbon Biomass in the North Pacific , 2002, Science.

[28]  A. Knap,et al.  Elemental C, N, and P cell content of individual bacteria collected at the Bermuda Atlantic Time‐series Study (BATS) site , 2002 .

[29]  C. Ridame,et al.  Chemical characterization of the Saharan dust end-member: Some biogeochemical implications for the western Mediterranean Sea , 2002 .

[30]  G. Eglinton,et al.  Composition, age, and provenance of organic matter in NW African dust over the Atlantic Ocean , 2002 .

[31]  David M. Karl,et al.  Dinitrogen fixation in the world's oceans , 2002 .

[32]  Elizabeth L. Mann,et al.  Copper toxicity and cyanobacteria ecology in the Sargasso Sea , 2002 .

[33]  Katarina Vrede,et al.  Elemental Composition (C, N, P) and Cell Volume of Exponentially Growing and Nutrient-Limited Bacterioplankton , 2002, Applied and Environmental Microbiology.

[34]  C. Ridame,et al.  Saharan input of phosphate to the oligotrophic water of the open western Mediterranean Sea , 2002 .

[35]  M. Maslin,et al.  Reduced effectiveness of terrestrial carbon sequestration due to an antagonistic response of ocean productivity , 2002 .

[36]  B. Biddanda,et al.  Small Players, Large Role: Microbial Influence on Biogeochemical Processes in Pelagic Aquatic Ecosystems , 2002, Ecosystems.

[37]  P. Holligan,et al.  Patterns of phytoplankton size structure and productivity in contrasting open-ocean environments , 2001 .

[38]  Robert W. Sanders,et al.  Responses of bacterioplankton and phytoplankton to organic carbon and inorganic nutrient additions in contrasting oceanic ecosystems , 2000 .

[39]  P. Burkill,et al.  Bacterial growth and grazing loss in contrasting areas of North and South Atlantic , 2000 .

[40]  G. Tarran,et al.  Picoplanktonic community structure on an Atlantic transect from 50°N to 50°S , 1998 .

[41]  P. Quay,et al.  Experimental determination of the organic carbon flux from open-ocean surface waters , 1997, Nature.

[42]  Roger Kerouel,et al.  Fluorometric determination of ammonia in sea and estuarine waters by direct segmented flow analysis , 1997 .

[43]  R. Rivkin,et al.  Inorganic nutrient limitation of oceanic bacterioplankton , 1997 .

[44]  Paul G. Falkowski,et al.  Evolution of the nitrogen cycle and its influence on the biological sequestration of CO2 in the ocean , 1997, Nature.

[45]  F. Rassoulzadegan,et al.  Accumulation of Degradable Doc in Surface Waters: Is It Caused by a Malfunctioning Microbial Loop? , 2022 .

[46]  J. Elser,et al.  Element ratios and growth dynamics of bacteria in an oligotrophic Canadian shield lake , 1996 .

[47]  J. Montoya,et al.  A Simple, High-Precision, High-Sensitivity Tracer Assay for N(inf2) Fixation , 1996, Applied and environmental microbiology.

[48]  N. Welschmeyer Fluorometric analysis of chlorophyll a in the presence of chlorophyll b and pheopigments , 1994 .

[49]  H. Ducklow,et al.  Annual flux of dissolved organic carbon from the euphotic zone in the northwestern Sargasso Sea , 1994, Nature.

[50]  J. Wilkinson Volatile production during contact metamorphism: the role of organic matter in pelites , 1991, Journal of the Geological Society.

[51]  R. Feely,et al.  Atmospheric iron inputs and primary productivity: Phytoplankton responses in the North Pacific , 1991 .

[52]  Patrick Raimbault,et al.  Feasibility of using an automated colorimetric procedure for the determination of seawater nitrate in the 0 to 100 nM range: Examples from field and culture , 1990 .

[53]  John H. Martin glacial-interglacial Co2 change : the iron hypothesis , 1990 .

[54]  B. Osborne,et al.  Light and Photosynthesis in Aquatic Ecosystems. , 1985 .

[55]  C. Trees,et al.  Physiological responses of Sargasso Sea picoplankton to nanomolar nitrate perturbations , 2007 .

[56]  I. Joint,et al.  Competition for inorganic nutrients between phytoplankton and bacterioplankton in nutrient manipulated mesocosms , 2002 .

[57]  Sallie W. Chisholm,et al.  Phytoplankton population dynamics at the Bermuda Atlantic Time-series station in the Sargasso Sea , 2001 .

[58]  R. Chester,et al.  Saharan dust inputs to the western Mediterranean Sea: depositional patterns, geochemistry and sedimentological implications , 1997 .

[59]  David C. Smith,et al.  A simple, economical method for measuring bacterial protein synthesis rates in seawater using 3H-leucine , 1992 .

[60]  R. Vannucci,et al.  Wind-blown dusts over the Central Mediterranean , 1984 .