Cell death in phytoplankton: correlation between changes in membrane permeability, photosynthetic activity, pigmentation and growth

By M. Veldhuis, G. Kraay, K. Timmermans. 2001

239 citations recorded by the source corpus.

Subfields: Ecology, Environmental Chemistry, Molecular Biology

View Paper: https://www.semanticscholar.org/paper/6acd4be5834038a8acb0a17f43564c9fe25d30a2

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Citations in the corpus

Dissolved organic matter (DOM) release by phytoplankton in the contemporary and future ocean (2014, background): “These processes include sloppy feeding by predators (Møller et al., 2003; Møller, 2007), lytic viral infections (Bratbak et al., 1993; Gobler et al., 1997, Bettarel et al., 2005), and cell death (Veldhuis et al., 2001).”
What is the role and nature of programmed cell death in phytoplankton ecology? (2006, background): “…activity assays has provided indirect evidence of mass lysis in phytoplankton communities (Brussaard et al., 1995; Agustı́ et al., 1998), whilst evidence from other physiological studies indicate that a considerable portion of cells in nature may not be viable (Veldhuis et al., 2001; Agustı́ 2004).”
Picophytoplankton - a comparative study of their biochemical composition and photosynthetic properties (2005, background): “not capable of cell division (Veldhuis et al., 2001).”
Dead or alive? Viability assessment of micro- and mesoplankton (2012, methodology): “SYTOXw Green has been predominantly used as a viability stain for phytoplankton species (e.g. Veldhuis et al., 1997, 2001) with only two studies related to zooplankton (Gill et al., 2003; Buttino et al., 2004).”
Physiological Structure and Single‐Cell Activity in Marine Bacterioplankton (2008, background): “Cell injury and damage results in increased membrane permeability that can be assessed using exclusion stains that bind to nucleic acids, such as propidium iodide (PI), TOPRO, or SYTOX Green (Veldhuis et al. 2001; Roth et al. 1997; Maranger et al. 2002).”
NUTRIENT LIMITATION AND HIGH IRRADIANCE ACCLIMATION REDUCE PAR AND UV‐INDUCED VIABILITY LOSS IN THE ANTARCTIC DIATOM CHAETOCEROS BREVIS (BACILLARIOPHYCEAE) 1 (2005, methodology): “Veldhuis et al. (2001) demonstrated that up to 50% of a population of small eukaryotes in samples from the North Atlantic was nonviable in the upper part of the photic zone, in contrast to samples from greater depths where the nonviable fraction comprised only 10% of the population.”
Growth physiology and fate of diatoms in the ocean: a review (2005, background): “Veldhuis et al. (2001) pub- lished detailed results of viability and cell death of, amongst others, Chaetoceros calcitrans.”
Determining the viability of marine protists using a combination of vital, fluorescent stains (2011, background): “First, chlorophyll molecules may remain intact within a dead cell for up to 2 weeks (Veldhuis et al. 2001; Garvey et al. 2007).”
Growth phase-specific release of polyunsaturated aldehydes by the diatom Skeletonema marinoi (2008, background): “late process in the cell death of diatoms, followed within one day by the destruction of the cell (Veldhuis et al., 2001), a massive PUA release due to autolysis would therefore likely be correlated with a decrease in the living cell density of the culture within the same day.”
GROWTH INHIBITION AND TOXICITY OF THE DIATOM ALDEHYDE 2‐TRANS, 4‐TRANS‐DECADIENAL ON THALASSIOSIRA WEISSFLOGII (BACILLARIOPHYCEAE) 1 (2005, methodology): “This process can be triggered both exogenously (bacterial or viral attack, nutrient limitation; Agustı́ and Duarte 2000) and/or endogenously (cell damage, senescence, death, genetically based automortality; Veldhuis et al. 2001).”
Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, unknown): “, 2012), and natural communities (Veldhuis et al., 2001).”