2017
DOI: 10.1038/s41598-017-14109-1
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Specific eukaryotic plankton are good predictors of net community production in the Western Antarctic Peninsula

Abstract: Despite our current realization of the tremendous diversity that exists in plankton communities, we have little understanding of how this biodiversity influences the biological carbon pump other than broad paradigms such as diatoms contributing disproportionally to carbon export. Here we combine high-resolution underway O2/Ar, which provides an estimate of net community production, with high-throughput 18 S ribosomal DNA sequencing to elucidate the relationship between eukaryotic plankton community structure a… Show more

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Cited by 23 publications
(34 citation statements)
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“…Phaeocystis has previously been reported as a key component of POC export in polar waters (DiTullio et al ), as they have the ability to form aggregates that sink rapidly out of the mixed layer (Arrigo ). However, during our study this eukaryotic phytoplankton appeared to contribute little to carbon transfer efficiency, especially compared to its diatom counterparts as observed elsewhere in Antarctic waters (Lin et al ). The rapid export of Phaeocystis out of the euphotic zone is generally related to their enhanced production of transparent exopolymer polysaccharides (TEP; Passow et al ).…”
Section: Resultssupporting
confidence: 61%
“…Phaeocystis has previously been reported as a key component of POC export in polar waters (DiTullio et al ), as they have the ability to form aggregates that sink rapidly out of the mixed layer (Arrigo ). However, during our study this eukaryotic phytoplankton appeared to contribute little to carbon transfer efficiency, especially compared to its diatom counterparts as observed elsewhere in Antarctic waters (Lin et al ). The rapid export of Phaeocystis out of the euphotic zone is generally related to their enhanced production of transparent exopolymer polysaccharides (TEP; Passow et al ).…”
Section: Resultssupporting
confidence: 61%
“…gDNA standard stock solutions and dilution concentrations were measured using a Qubit 3.0 fluorometer (Thermo Fisher Scientific, Waltham, MA, USA). After spiking in internal standards, DNA extraction was performed as described previously (8).…”
Section: Methodsmentioning
confidence: 99%
“…PCRs were performed in triplicates for each sample. 18S rRNA gene PCR and library pooling were performed as described previously (8). 16S rRNA gene library construction was similar to that for 18S rRNA gene except that 2 U of Platinum Taq DNA high-fidelity polymerase (Invitrogen) was added to each reaction mixture, and the PCR annealing temperature was 60°C.…”
Section: Methodsmentioning
confidence: 99%
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