A comparison of future increased CO2 and temperature effects on sympatric Heterosigma akashiwo and Prorocentrum minimum

By Feixue Fu, Yaohong Zhang, Mark E. Warner, Yuanyuan Feng, Jun Sun, D. Hutchins. 2008

156 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/30242701e03ea7ed7649ee62f92a0fe54f7b49db

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In Oceanography

Citations in the corpus

Co2 and phosphate availability control the toxicity of the harmful bloom dinoflagellate Karlodinium veneficum. (2010, methodology): “Semi-continuous culturing methods were used to measure the effects of PO43– availability and/or pCO2 levels during acclimated 56 Fu et al.: CO2 and phosphate availability controls karlotoxin production steady-state growth (Hutchins et al. 2007, Fu et al. 2008).”
Harmful algal blooms and climate change: Learning from the past and present to forecast the future (2015, background): “For example exposure of the harmful algal bloom species Heterosigma akashiwo to lower pH increased its photosynthetic growth rates (Fu et al., 2008; Nimer et al., 1997) and substantially increased its swimming speed (30%) and downward velocities (46%), implying that changing pCO2 is a signaling fact”
Interactions between changing pCO2, N2 fixation, and Fe limitation in the marine unicellular cyanobacterium Crocosphaera (2008, methodology): “…(Burkhardt and Riebesell 1997; Tortell et al. 2002), cyanobacteria (Fu et al. 2007; Hutchins et al. 2007), coccolithophores (Feng et al. 2008), and harmful bloom flagellates (Fu et al. 2008), the effects of changing seawater pCO2 on unicellular N2-fixing cyanobacteria have not been examined.”
Influence of temperature, salinity and irradiance on the growth and cell yield of the harmful red tide dinoflagellate Alexandrium catenella colonizing Mediterranean waters (2011, background): “Temperature impacts many physiological processes in HABs, such as division rate, photosynthesis, toxin production and respiration (Cembella, 1998; Nagasoe et al., 2006; Fu et al., 2008; Xu et al., 2010).”
Differential effects of ocean acidification on growth and photosynthesis among phylotypes of Symbiodinium (Dinophyceae) (2011, methodology): “Values of E(l) and a(l) were measured between 40 and 750 nm with a spectroradiometer (SR-9910a, Macam) and a spectrophotometer (U-3000, Hitachi High Technologies), respectively, following Suggett et al. (2008). Values for ā were determined on the basis of the spectral output for the blue LEDs (āLED)”
Response of Antarctic, temperate, and tropical microalgae to temperature stress (2013, background): “Rising CO2 and temperature over the coming decades may stimulate the growth of the harmful raphidophyte Heterosigma more than that of the dinoflagellate Prorocentrum, possibly favoring the former in interspecific competition (Fu et al. 2008).”
Can increases in temperature stimulate blooms of the toxic benthic dinoflagellate Ostreopsis ovata (2011, background): “, 2006) and the raphidophyte Heterosigma akashiwo (Fu et al., 2008) have also been shown to be enhanced by high seawater temperatures.”
The C:N:P stoichiometry of organisms and ecosystems in a changing world: A review and perspectives (2012, background): “:P ratios of some cyanobacteria increased in response to elevated environmental [CO2] levels (Fu et al., 2007; Hutchins et al., 2007), but other studies did not observe this effect (Fu et al., 2008; Bellerby et al., 2008).”
The effect of ocean acidification on symbiont photorespiration and productivity in Acropora formosa (2010, background): “Accordingly, in free-living dinoflagellates with a CCM, such as Protoceratium reticulatum, the effect of increasing CO2 has been shown to have little effect on growth (Ratti et al., 2007; Fu et al., 2008).”
Phytoplankton in a changing world: cell size and elemental stoichiometry (2010, background): “The slope and intercept are affected by the taxonomic composition of the data set and the growth conditions for each species (see text for discussion). changes in irradiance, temperature and carbon-dioxide (Finkel et al., 2006; Fu et al., 2007; Hutchins et al., 2007; Fu et al., 2008).”
Responses of marine benthic microalgae to elevated CO2 (2011, unknown): “Experimental studies of bloom-forming cyanobacteria usually show a positive response to CO 2 enrichment (Barcelos e Ramos et al. 2007; Hutchins et al. 2007; Levitan et al. 2007; Fu et al. 2008a; Kranz et al. 2009).”