Regeneration and utilization of nutrients during collapse of a Mesodinium rubrum red tide and its influence on phytoplankton species composition

[1]  Matthew D. Johnson,et al.  Jumping and overcoming diffusion limitation of nutrient uptake in the photosynthetic ciliate Mesodinium rubrum , 2017 .

[2]  Richard C. Dugdale,et al.  Pluses and minuses of ammonium and nitrate uptake and assimilation by phytoplankton and implications for productivity and community composition, with emphasis on nitrogen‐enriched conditions , 2016 .

[3]  Bo-Cai Gao,et al.  Space station image captures a red tide ciliate bloom at high spectral and spatial resolution , 2015, Proceedings of the National Academy of Sciences.

[4]  D. Anderson,et al.  Role of dissolved nitrate and phosphate in isolates of Mesodinium rubrum and toxin-producing Dinophysis acuminata. , 2015, Aquatic microbial ecology : international journal.

[5]  A. Buchan,et al.  Master recyclers: features and functions of bacteria associated with phytoplankton blooms , 2014, Nature Reviews Microbiology.

[6]  P. Glibert,et al.  Phytoplankton communities from San Francisco Bay Delta respond differently to oxidized and reduced nitrogen substrates—even under conditions that would otherwise suggest nitrogen sufficiency , 2014, Front. Mar. Sci..

[7]  A. D. Vethaak,et al.  Seasonal variability in irradiance affects herbicide toxicity to the marine flagellate Dunaliella tertiolecta , 2014, Front. Mar. Sci..

[8]  Z. Lai,et al.  Physical-biological coupling induced aggregation mechanism for the formation of high biomass red tides in low nutrient waters. , 2014, Harmful algae.

[9]  D. Morse,et al.  Putting the N in dinoflagellates , 2013, Front. Microbiol..

[10]  H. Jeong,et al.  The red-tide ciliate Mesodinium rubrum in Korean coastal waters , 2013 .

[11]  Jong Soo Park,et al.  Sequestered plastids in Mesodinium rubrum are functionally active up to 80 days of phototrophic growth without cryptomonad prey , 2013 .

[12]  P. Leavitt,et al.  Phytoplankton-Specific Response to Enrichment of Phosphorus-Rich Surface Waters with Ammonium, Nitrate, and Urea , 2013, PloS one.

[13]  J. Burkholder,et al.  Misuse of the phytoplankton-zooplankton dichotomy : the need to assign organisms as mixotrophs within plankton functional types , 2013 .

[14]  F. Wilkerson,et al.  The effect of inorganic nitrogen speciation on primary production in the San Francisco Estuary , 2012 .

[15]  Lee Ann McCue,et al.  Red Waters of Myrionecta rubra are Biogeochemical Hotspots for the Columbia River Estuary with Impacts on Primary/Secondary Productions and Nutrient Cycles , 2012, Estuaries and Coasts.

[16]  P. Leavitt,et al.  Comparative effects of urea, ammonium, and nitrate on phytoplankton abundance, community composition, and toxicity in hypereutrophic freshwaters , 2011 .

[17]  Xingyu Song,et al.  Phytoplankton biomass and production in northern South China Sea during summer: Influenced by Pearl River discharge and coastal upwelling , 2011 .

[18]  J. Raven The cost of photoinhibition. , 2011, Physiologia plantarum.

[19]  G. Saba,et al.  The effects of harmful algal species and food concentration on zooplankton grazer production of dissolved organic matter and inorganic nutrients , 2011 .

[20]  R. Sinsabaugh,et al.  Integrating resource utilization and temperature in metabolic scaling of riverine bacterial production. , 2010, Ecology.

[21]  G. Kling,et al.  Temperature controls on aquatic bacterial production and community dynamics in arctic lakes and streams. , 2010, Environmental microbiology.

[22]  K. Flynn,et al.  Modelling mixotrophy in harmful algal blooms: More or less the sum of the parts? , 2010 .

[23]  P. Qian,et al.  Is inorganic nutrient enrichment a driving force for the formation of red tides? A case study of the dinoflagellate Scrippsiella trochoidea in an embayment , 2008 .

[24]  Richard C. Dugdale,et al.  The role of ammonium and nitrate in spring bloom development in San Francisco Bay , 2007 .

[25]  F. Wilkerson,et al.  Phytoplankton blooms and nitrogen productivity in San Francisco Bay , 2006 .

[26]  T. Fenchel,et al.  Motile behaviour of the bloom-forming ciliate Mesodinium rubrum , 2006 .

[27]  Louis A. Codispoti,et al.  The Role of Eutrophication in the Global Proliferation of Harmful Algal Blooms , 2005 .

[28]  H. Jeong,et al.  Ingestion of cryptophyte cells by the marine photosynthetic ciliate Mesodinium rubrum , 2004 .

[29]  Patricia M. Glibert,et al.  Interactions of top-down and bottom-up control in planktonic nitrogen cycling , 2004, Hydrobiologia.

[30]  K. Yin Influence of monsoons and oceanographic processes on red tides in Hong Kong waters , 2003 .

[31]  J. Burkholder,et al.  Harmful algal blooms and eutrophication: Nutrient sources, composition, and consequences , 2002 .

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

[33]  M. Lomas,et al.  Ammonium release by nitrogen sufficient diatoms in response to rapid increases in irradiance , 2000 .

[34]  Matthew D. Johnson,et al.  Cryptophyte algae are robbed of their organelles by the marine ciliate Mesodinium rubrum , 2000, Nature.

[35]  M. Lomas,et al.  Temperature regulation of nitrate uptake: A novel hypothesis about nitrate uptake and reduction in cool‐water diatoms , 1999 .

[36]  I. Koike,et al.  Direct Determination of Carbon and Nitrogen Contents of Natural Bacterial Assemblages in Marine Environments , 1998, Applied and Environmental Microbiology.

[37]  D. Purdie,et al.  Recurrent Red-tides in the Southampton Water Estuary Caused by the Phototrophic CiliateMesodinium rubrum , 1997 .

[38]  Y. Qi,et al.  The abundance cycle and influence factors on red tide phenomena of Noctiluca scintillans (Dinophyceae) in Dapeng Bay, the South China Sea , 1997 .

[39]  G. Bratbak,et al.  Viral control of Emiliania huxleyi blooms , 1996 .

[40]  M. Kyle,et al.  Ratios of carbon, nitrogen and phosphorus in Pseudomonas fluorescens as a model for bacterial element ratios and nutrient regeneration , 1996 .

[41]  Andrew G. Dickson,et al.  Protocols for the Joint Global Ocean Flux Study (JGOFS) Core Measurements , 1996 .

[42]  H. Ducklow,et al.  Temperature and substrate regulation of bacterial abundance, production and specific growth rate in Chesapeake Bay, USA , 1994 .

[43]  J. Raven Physiology of inorganic C acquisition and implications for resource use efficiency by marine phytoplankton: relation to increased CO2 and temperature , 1991 .

[44]  N. M. Price,et al.  Comparison of methods for the analysis of dissolved urea in seawater , 1987 .

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

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

[47]  J. C. Goldman,et al.  Nitrogenous Nutrition of Marine Phytoplankton in Nutrient-Depleted Waters , 1979, Science.

[48]  G. Slawyk,et al.  Comparison of two automated ammonium methods in a region of coastal upwelling , 1972 .