Dilution experiments were conducted during four “cycle” experiments on BLOOFINZ cruise RR2201. For each experiment, seawater was collected from Niskin bottles on early-morning CTD hydrocasts (~02:00 local time) at 6 depths in the euphotic zone. For each depth sampled, a two-treatment dilution experiment (Landry et al., 2008, 2011) was prepared, with one polycarbonate bottle (2.7 L) containing unfiltered seawater (100%) and the second (diluted) bottle consisting of ~33% whole seawater with filtered water from the same depth. Seawater was filtered directly from the Niskin bottles using a peristaltic pump, silicone tubing and an in-line 0.2 µm Suporcap (Pall Acro) filter capsule that had previously been acid washed (3.7% trace-metal grade HCl; Milli-Q and seawater rinses). All bottles were secured in coarse net bags clipped to the line of a drogued, satellite-tracked drifter and incubated in situ for 24 h at the depth of collection. Initial and final samples (250 mL) for FlChla were filtered onto GF/F filters and extracted with 90% acetone in a -20°C freezer for 24 h and analyzed on a Turner Designs model 10 fluorometer. Samples (2.3 L) for HPLC analyses of chlorophyll and carotenoid pigments were concentrated onto GF/F filters under low vacuum pressure, immediately frozen in liquid nitrogen and stored at -80°C. The samples were extracted for 2 h in 100% methanol, disrupted by sonication, clarified by GF/F filtration and analyzed (Agilent Technologies 1200 Series) at the analytical facility of the Institut de la Mer de Villefranche (CNRS-France).