Nitrogen utilization by the raphidophyte Heterosigma akashiwo: Growth and uptake kinetics in laboratory cultures
By J. Herndon, W. Cochlan. 2007
133 citations recorded by the source corpus.
Subfields: Environmental Chemistry, Oceanography, Renewable Energy, Sustainability and the Environment
View Paper: https://www.semanticscholar.org/paper/0b433f8457f23117d345b42f72eb8cba95ac0065
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Citations in the corpus
- DON as a source of bioavailable nitrogen for phytoplankton (2006, unknown): “In particular, it appears that some harmful algae species are capable of using DON for nutrition and may prefer it to inorganic sources (e.g. Lomas et al., 1996; Berg et al., 1997; Herndon and Cochlan, 2007).”
- Eutrophication and Harmful Algal Blooms: A Scientific Consensus (2008, background): “For example, assessments of specific relationships that are required in models (such as parameters of nutrient uptake and growth kinetics) are better resolved under laboratory conditions where a culture of known physiological state can be established and where environmental conditions can be rigorou”
- Mixotrophy, a major mode of nutrition for harmful algal species in eutrophic waters (2008, background): “Heterosigma akashiwo Uptake and growth on urea, glutamic acid (Zhang et al., 2006; Herndon and Cochlan, 2007)”
- 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, result): “Consistent with this hypothesis, several studies have shown that some phytoplankton species grown on NH14 or urea have higher growth rates than on NO 2 3 (e.g., Herndon and Cochlan 2007; Solomon et al. 2010 and references therein), although this is far from a universal observation.”
- Harmful algal blooms and climate change: Learning from the past and present to forecast the future (2015, background): “…nutrient conditions, due perhaps to higher physiological quota requirements; e.g., Alexandrium spp. (Collos et al., 2006), Heterosigma akashiwo (Herndon and Cochlan, 2007), Noctiluca spp. (Harrison et al., 2011), Prorocentrum spp. (Anderson et al., 2012); or perhaps it is a consequence of the…”
- Role of urea in microbial metabolism in aquatic systems: a biochemical and molecular review (2010, background): “In some cases, growth was faster on urea than NO3– and NH4+ at a lower irradiance; this pattern could be seen for Chaetoceros gracilis, Dunaliella tertiolecta, and Heterosigma akashiwo (Levasseur et al. 1993, Herndon & Cochlan 2007; Table 1).”
- Harmful algal blooms and eutrophication: Examining linkages from selected coastal regions of the United States (2008, background): “Isolates of both H. akashiwo and P. cuspidata from the Pacific Northwest can grow equally well on NH 4 + and NO 3 À when supplied as the sole N source (Auro et al., 2006; Herndon and Cochlan, 2007; Auro, 2007), so there is a potential for anthropogenic stimulation of these blooms.”
- Linking the physiology and ecology of Cochlodinium to better understand harmful algal bloom events: A comparative approach (2008, background): “88 Herndon and Cochlan (2006) Gymnodinium catenatum 207.”
- Fraser River sockeye salmon marine survival decline and harmful blooms of Heterosigma akashiwo. (2010, background): “42mg-at N L 1 for NH4 , NO3 and urea, respectively, and any of these substrates could maintain a bloom (Herndon and Cochlan, 2007).”
- Factors influencing the initiation of blooms of the raphidophyte Heterosigma akashiwo and the diatom Skeletonema costatum in a port in Japan (2008, background): “Considering the half-saturation constant of 0.40 mmol L21 for nitrate uptake of S. costatum (Eppley et al. 1969), which is much lower than the 1.47–2.45 mmol L21 for H. akashiwo (Tomas 1979; Herndon and Cochlan 2007), the same applies to the maintenance of a S. costatum bloom.”