2016
DOI: 10.1002/lno.10360
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Cellular characteristics and growth behavior of iron‐limited Microcystis aeruginosa in nutrient‐depleted and nutrient‐replete chemostat systems

Abstract: Cellular responses of Fe‐limited Microcystis aeruginosa were investigated under nutrient‐depleted and ‐replete conditions. Cellular growth, Fe quota and Fe uptake kinetics were examined in chemostat systems using nutrient‐replete Fraquil* (where all nutrients except for Fe are present at sufficient level to achieve optimal growth) and nutrient‐deplete Fraquil* (where some nutrients in addition to Fe are potentially growth‐limiting factors). For both nutrient conditions, cellular Fe quota increased with increas… Show more

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Cited by 7 publications
(4 citation statements)
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References 64 publications
(105 reference statements)
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“…This study joins a growing list that have observed an important role of micronutrients in structuring phytoplankton communities and increasing cyanobacterial growth in physically and chemically diverse freshwater systems. For example, Downs et al (2008) noted a stimulation of the cyanobacterium Anabaena flos-aquae upon addition of cobalt, copper, manganese and a trace metal mixture, while a number of studies have observed iron limitation of cyanobacteria growth (Wever et al 2008;Molot et al 2010;Harland et al 2013;Fujii et al 2016).…”
Section: Discussionmentioning
confidence: 99%
“…This study joins a growing list that have observed an important role of micronutrients in structuring phytoplankton communities and increasing cyanobacterial growth in physically and chemically diverse freshwater systems. For example, Downs et al (2008) noted a stimulation of the cyanobacterium Anabaena flos-aquae upon addition of cobalt, copper, manganese and a trace metal mixture, while a number of studies have observed iron limitation of cyanobacteria growth (Wever et al 2008;Molot et al 2010;Harland et al 2013;Fujii et al 2016).…”
Section: Discussionmentioning
confidence: 99%
“…Dissolved unchelated Fe(II) (Fe(II)') arising from the photoreductive dissociation of Fe(III)-EDTA has been shown to be the major Fe substrate in EDTA-buffered culture medium at pH 8 (Fujii et al, 2011b;Dang et al, 2012;Fujii et al, 2016). Here, the steady-state concentration of Fe(II)' was calculated using the same kinetic model and assuming that Fe(II)' is the major form of Fe available for uptake by R. raciborskii (SI4 and Table S2 in the Supporting Information respectively).…”
Section: Discussionmentioning
confidence: 99%
“…A growing body of literature demonstrates the impact of trace metals (alone or in combination with macronutrients) on phytoplankton growth [34,69,70,71,72]. For example, Downs et al [35] observed that the addition of Cu, Mo or Co during a cyanobacterial bloom in a eutrophic lake stimulated primary productivity by up to 40%, indicating a large contribution of micronutrients to eutrophication.…”
Section: Importance Of Trace Metalsmentioning
confidence: 99%
“…Culture-based experiments form most of the literature on cyanobacteria–metal interactions (≈63% of the studies from Table 1). While culture experiments often demonstrate unambiguous relationships between a single species growth and a given micronutrient, as demonstrated by Fujii et al [70], it is also important to examine these relationships under field conditions which take into account environmentally relevant concentrations of trace metals, particularly as selective pressures and behaviours of culture-raised organisms can differ from those in natural systems [94]. Nutrient amendment bioassays are a useful tool in bridging the gap between culture and field studies, and have been used effectively in studies such as de Wever et al [64] and Zhang et al [37].…”
Section: Knowledge Gapsmentioning
confidence: 99%