@article {Stawiarski2016,
	title = {The physiological response of picophytoplankton to temperature and its model representation},
	journal = {Fronitiers in Marine Science},
	volume = {3},
	number = {164},
	year = {2016},
	note = {tex.mendeley-tags: rcc162,rcc1677,rcc212,rcc289,rcc296,rcc30,rcc361,rcc438,rcc503},
	pages = {1{\textendash}13},
	keywords = {chlorophyll a to carbon, chlorophyll a to carbon ratio, Eppley, frontiers in marine science, frontiersin, org, physiological parameterization, phytoplankton growth rates, phytoplankton size scaling, picoeukaryotes, picophytoplankton, ratio, rcc162, rcc1677, rcc212, rcc289, rcc296, rcc30, rcc361, rcc438, rcc503, temperature tolerance, www},
	issn = {2296-7745},
	doi = {10.3389/fmars.2016.00164},
	author = {Stawiarski, Beate and Buitenhuis, Erik T and Qu{\'e}r{\'e}, Corinne Le}
}
@article {Giovagnetti2012,
	title = {Growth and photophysiological responses of two picoplanktonic {\textexclamdown}i{\textquestiondown}Minutocellus species{\textexclamdown}/i{\textquestiondown}, strains RCC967 and RCC703 (Bacillariophyceae)},
	journal = {European Journal of Phycology},
	volume = {47},
	number = {4},
	year = {2012},
	note = {ISBN: 0967-0262 tex.mendeley-tags: rcc703,rcc967},
	pages = {408{\textendash}420},
	abstract = {Reaching up to 50\% of the total biomass in oligotrophic waters and armed with a set of ecological and biological properties related to their small size, picophytoplankton ({\textexclamdown}3.0 mm) are a good model to address ecophysiological questions regarding phytoplankton biodiversity. Two picoplanktonic diatoms, one isolated from an upwelling ecosystem in the Pacific Ocean (Minutocellus sp., strain RCC967), and another from oceanic waters in the Indian Ocean (Minutocellus sp., strain RCC703) were used to test hypotheses on the functional relation between ecological niche adaptation and photosynthetic regulation capacity and efficiency. Cultures were subjected to five sine light climates, each one set to peak at a different photon flux density, respectively 10, 50, 100, 250 and 500 mmol photons m(-2) s(-1). Growth rate, photosynthesis, non-photochemical fluorescence quenching, pigment composition, and particulate organic carbon and nitrogen content were followed daily for 5 days. Growth rate and physiological response curves were different in the two species, in agreement with their distinct habitats of origin. Such differences could be related to the diverse photoacclimative strategies displayed by the two species, revealing a clear adaptive divergence despite their close taxonomic relationship. Photoacclimative strategies of the two picoplanktonic diatoms are discussed in the light of functional diversity and ecosystem adaptation.},
	keywords = {carbon, diatoms, elemental stoichiometry, fluctuating light, marine-phytoplankton, non-photochemical fluorescence quenching, phaeodactylum-tricornutum, photoacclimation, photoprotection, photoregulation, Photosynthesis, picoeukaryotes, planktonic diatoms, rcc703, rcc967, RCC?o?dd, violaxanthin cycle, Xanthophyll cycle, xanthophyll-cycle activity},
	doi = {10.1080/09670262.2012.733030},
	author = {Giovagnetti, V and Cataldo, M L and Conversano, F and Brunet, C}
}
@article {Worden2006,
	title = {Picoeukaryote diversity in coastal waters of the Pacific Ocean},
	journal = {Aquatic Microbial Ecology},
	volume = {43},
	number = {2},
	year = {2006},
	note = {tex.mendeley-tags: Micromonas,RCC,rcc},
	pages = {165{\textendash}175},
	abstract = {The extraordinary molecular phylogenetic diversity of picoeukaryotes and their contributions to marine processes have been highlighted recently. Herein, picoeukaryotic diversity in the coastal Pacific Ocean is characterized for the first time, Close to full length small subunit ribosomal RNA (ssu rRNA) gene amplicons were cloned and sequenced from size fractionated samples ({\textexclamdown} 2 mu m) taken between September 2000 and October 2001. Sequences belonging to the order Mamiellales were abundant, with Micromonas pusilla-like sequences in all 5 libraries (4 operational taxonomic units, OTUs, at {\textquestiondown}= 99\% sequence similarity), Ostreococcus in 4 (1 OTU) and Bathycoccus in 2 (1 OTU). Phylogenetic reconstruction showed distinct Micromonas clades at this site (although not for other Mamiellales), supporting the idea that the designation M pusilla harbors cryptic species. In combination with picophytoplankton dynamics previously reported for the same period, the data indicates that picoplanktonic primary production at this site is likely to be dominated by prasinophytes. Furthermore, a Micromonas-clade with no cultured representatives was identified bearing highest identity to Sargasso Sea shotgun clone sequences. Comparison of the Pacific sequences with the shotgun clones showed Ostreococcus and Micromonas at 1 Sargasso site with elevated chlorophyll (chl) levels, but not at other Sargasso sites. Other Pacific clones were primarily Novel Alveolate Group II, which were highly diverse based on OTU analyses. Novel Alveolate Group 1, Ciliophora, Cercozoa-like and stramenopile sequences were also retrieved. Although picoeukaryotic diversity has been characterized in only 1 other Pacific Ocean sample (equatorial Pacific), most stramenopile and alveolate sequences corresponded to previously identified phylogenetic clades from studies conducted in other oceans and for which no cultured representatives exist.},
	keywords = {18s rdna sequences, 18S rRNA, community structure, diversity, english-channel, eukaryotic picoplankton, global dispersal, Micromonas, north-atlantic, phylogenetic analysis, picoeukaryotes, picophytoplankton, picoplankton, prasinophytes, pusilla, rcc, RIBOSOMAL-RNA GENE, sargasso sea, small subunit, vibrio-cholerae},
	doi = {10.3354/ame043165},
	author = {Worden, A Z}
}
