Physiological Structure and Single‐Cell Activity in Marine Bacterioplankton
By Paul A. del Giorgio, J. Gasol. 2008
158 citations recorded by the source corpus.
Subfields: Ecology, Endocrinology, Oceanography
View Paper: https://www.semanticscholar.org/paper/6d7898665eaab884a9d1fdfdd91bd390c89632a8
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Citations in the corpus
- Microbial Respiration, the Engine of Ocean Deoxygenation (2019, background): “…rates (Table 2) tend not to be correlated with temperature due to the ∼50-fold variability in cell specific respiration rates (0.1 to 5 fmol C cell−1 day−1; Baltar et al., 2009a,b) related to the lack of a strong relationship between cell abundance and cell activity (del Giorgio and Gasol, 2008).”
- Xenobiotics shape the physiology and gene expression of the active human gut microbiome (2013, unknown): “Bacterial Physiology Bacterial physiology was assessed with three fluorescent stains (Figure 1A): propidium iodide (Pi), bis-(1,3-dibutylbarbituric acid)trimethine oxonol [DiBAC4(3)], and SybrGreen I, allowing the observation of cells with loss of membrane integrity and membrane polarity and with di”
- Microbial oceanography of the dark ocean's pelagic realm (2009, result): “…16–20% of the heterotrophic prokary- otic community of the meso- and bathypelagic North Atlantic is taking up leucine and can be considered as metabolically active (Herndl et al. 2005; Teira et al. 2006a), a percentage similar to that reported for epipelagic waters (del Giorgio and Gasol 2008).”
- Fundamentals of Microbial Community Resistance and Resilience (2012, background): “Evidence suggests that microorganisms may use dormancy in a variety of other situations as well, for example when challenged by unfavorable temperatures (Whitesides and Oliver, 1997), starvation (del Giorgio and Gasol, 2008), or predator-induced mortality (Pearl et al., 2008).”