2008
DOI: 10.3354/ame01187
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Effects of temperature on photosynthetic parameters and TEP production in eight species of marine microalgae

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Cited by 181 publications
(174 citation statements)
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References 39 publications
(61 reference statements)
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“…In line with this, the analysis of the composition of the dcCHO pool for the AQ2 experiment showed a predominant accumulation of combined glucose )that is a main storage component of algal cells. While a stimulating effect of warming on primary production and the release of carbonrich compounds has also been reported from other studies (Verity 1981;Davison 1991;Wolfstein et al 2002;Morán et al 2006;Claquin et al 2008), the here determined rates of dissolved PP, however, either showed a negative (AQ2; Fig. 2) or no response to rising temperature (AQ5, AQ6; Fig.…”
Section: Temporal Dynamics Of Bloom Developmentmentioning
confidence: 58%
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“…In line with this, the analysis of the composition of the dcCHO pool for the AQ2 experiment showed a predominant accumulation of combined glucose )that is a main storage component of algal cells. While a stimulating effect of warming on primary production and the release of carbonrich compounds has also been reported from other studies (Verity 1981;Davison 1991;Wolfstein et al 2002;Morán et al 2006;Claquin et al 2008), the here determined rates of dissolved PP, however, either showed a negative (AQ2; Fig. 2) or no response to rising temperature (AQ5, AQ6; Fig.…”
Section: Temporal Dynamics Of Bloom Developmentmentioning
confidence: 58%
“…2). Similarly, a stimulation of TEP production and aggregation by rising temperature has been previously reported for various monoalgal cultures (Thornton and Thake 1998;Claquin et al 2008). In AQ5, this first peak was followed by a decline in TEP under in situ temperature conditions, whereas the concentration further increased in the postbloom phase of the elevated temperature treatments, thus yielding an overall significant temperature response (Table 5; Fig.…”
Section: Tep Dynamicsmentioning
confidence: 78%
“…Field observations showed that cyanobiont cells concentrate in the center of Trichodesmium colonies, and cell motility would indicate that the hetDA cells preferentially inhabits this niche within the colony. It is well known that algae can release significant amounts of recently fixed carbon as molecules and polymers that fall into both the dissolved or particulate phases, and Trichodesmium is no exception (e.g., Nagata, 2000;Berman-Frank et al, 2007;Claquin et al, 2008). In Trichodesmium, this carbon (and presumably N) supports a wide array of heterotrophic organisms (Paerl and Bebout, 1989;Hmelo et al, 2012) with activities so significant that the center of the colonies can go anoxic (Paerl and Bebout, 1988) and even allow the growth of active denitrifying bacteria (Wyman et al, 2013).…”
Section: Discussionmentioning
confidence: 99%
“…Aggregate formation at elevated temperature has been hypothesized to be due to sticky polymers on the surface of the diatoms (Thornton & Thake, 1998) or the production of TEP . Seven of eight phytoplankton species studied by Claquin et al (2008) produced more TEP with increasing temperature when grown in batch culture. The trend continued until a maximum TEP production rate was reached, with higher temperatures resulting in lower TEP production rates.…”
Section: Temperature and Stratificationmentioning
confidence: 99%
“…Exudation by phytoplankton plays a significant role in the formation of TEP (Passow, 2002b;Gärdes et al, 2011). Numerous studies have shown that exopolymer particles accumulate in phytoplankton cultures (Passow, 2002b;Claquin et al, 2008;Fukao et al, 2010) and during blooms (Passow et al, 1994;Engel et al, 2002;Engel, 2004;Harlay et al, 2009) (Figs 3,5). Generally, TEP are not exuded directly by phytoplankton cells; they form abiotically from precursors released by cells.…”
Section: 4mentioning
confidence: 99%