2017
DOI: 10.1016/j.ecss.2015.08.015
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Ocean acidification effect on prokaryotic metabolism tested in two diverse trophic regimes in the Mediterranean Sea

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Cited by 25 publications
(23 citation statements)
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“…6a), agreeing with other ocean acidification studies globally that have reported an increase in abundance of picophytoplankton at elevated CO 2 levels (e.g. Brussaard et al, 2013;Schulz et al, 2013;Biswas et al, 2015;Crawfurd et al, 2017). However, studies on phytoplankton communities in other Antarctic regions have reported shifts towards larger diatom species (Ross Sea; Feng et al, 2010;Tortell et al, 2008) or no change (Antarctic Peninsula;Young et al, 2015).…”
Section: Nano-and Picophytoplanktonsupporting
confidence: 86%
See 1 more Smart Citation
“…6a), agreeing with other ocean acidification studies globally that have reported an increase in abundance of picophytoplankton at elevated CO 2 levels (e.g. Brussaard et al, 2013;Schulz et al, 2013;Biswas et al, 2015;Crawfurd et al, 2017). However, studies on phytoplankton communities in other Antarctic regions have reported shifts towards larger diatom species (Ross Sea; Feng et al, 2010;Tortell et al, 2008) or no change (Antarctic Peninsula;Young et al, 2015).…”
Section: Nano-and Picophytoplanktonsupporting
confidence: 86%
“…Despite the apparent resilience of prokaryotes to ocean acidification, several authors suggest they may be indirectly affected by changes in substrate availability due to changes in phytoplankton composition and abundance (e.g. Piontek et al, 2010;Celussi et al, 2017). Given the critical role of heterotrophic prokaryotes in remineralisation and carbon flux, it is vital to better understand the direct and indirect effects of ocean acidification on their communities.…”
Section: Introductionmentioning
confidence: 99%
“…For the field measurement of enzymatic activities, the fluorimetric method is a widespread technique generally used in aquatic environments, even if specific knowledge about the macromolecular structure of the organic matter in the ocean is lacking. According to the Hoppe's method [30], specific artificial substrates are widely used to measure potential enzyme activities in seawater and sediments. These substrate analogues consist of a monomer [an amino acid or a monosaccharide analogue] linked to a fluorophore, such as L-leucine-7-amido-4-methylcoumarin hydrochloride (leucine-MCA), used to measure leucine aminopeptidase; 4-methylumbelliferyl-β-D-glucopyranoside (MUF-β-glucose), and methylumbelliferyl-phosphate, used to measure β-glucosidase and phosphatase activities respectively.…”
Section: Enzymatic Activitiesmentioning
confidence: 99%
“…According to the kinetic approach, it is possible to determine also the Michaelis-Menten constant (Km), which expresses the affinity of an enzyme for its substrate [6],[30].…”
Section: Enzymatic Activitiesmentioning
confidence: 99%
“…Our new data showed that in low‐latitude, oligotrophic warm waters, when the growth of phytoplankton was suppressed, the bacterioplankton community could be significantly affected by acidification in the early phases of incubation (first 6 days), while acidification had little effect in nutrient depleted conditions (postbloom). Other studies have also observed that changes to bacterial community composition after acidification may be linked to nutrient conditions (Bunse et al, ; Celussi et al, ; Hornick et al, ). We observed relatively low bacterial diversity (Figure ) and relatively simple network of microbial community (Figure ) under high CO 2 compared to the control microcosm.…”
Section: Discussionmentioning
confidence: 94%