Sample collection
Live specimens were collected in vertical tows within the upper 200 m using a 1 m ring net of mesh size 280 m m with a 20 liter protected cod-end. Each tow was conducted at the same MOCNESS tow location soon after the MOCNESS was retrieved. The net was hauled at 10-15 m per min. After the net was retrieved, the cod-end was immediately transported to a dark temperature-controlled room to simulate the ocean water temperature (-1° C). The cod-end content was gently poured into a 20 liter bucket filled with GF/F filtered seawater at room temperature and then subdivided in 2 size classes using 2 large diameter sieves of 303 and 500
mm. Each sieve was successively transferred to a second and then a third bucket with GF/F filtered seawater to remove any traces of phytoplankton. Sequential samples were taken at short time intervals. Samples were immediately filtered by GF/F filters, stored in petri dishes and frozen at -80°C. Incubation and sampling were conducted up to 6 hrs after the net tow.Frozen samples were transported in dry ice back to the laboratory in La Jolla, CA, and were kept frozen at -80°C until they were analyzed.
Analysis
Samples were picked by species and stages under a dissecting stereoscope. The frozen GF/F filter was placed in a petri dish refrigerated by a cold plate. Nitrogen gas was blown into the sample to avoid excessive condensation on the samples and the scope. Chlorophyll and phaeopigment were extracted in methanol and measured using a Turner fluorometer. The number of animals in the analysis is typically 2-5 individuals of large copepods (1000-2000 m m), 5-10 for medium size copepods (500-1000 m m) and 10-50 for small copepods (200-500
mm).The theoretical basis of this experiment is that we assume that the rate of ingestion to be proportional to the rate of gut evacuation. The ingestion rate (I) is obtained from:
I=k P0
where P0 is the initial concentration of gut pigment in fresh-caught field animals, and the rate of evacuation was obtained from :
Pt = P0 e-kt
where Pt is the gut pigment after time t and k the evacuation rate constant. The evacuation rate is estimated by
k=ln(P0/Pt)/t