The diel cycle in the integrated particle load in the equatorial Pacific: A comparison with primary production

As part of the U.S. JGOFS EqPac process study beam c profiles were obtained during two time-series occupations of the equator at 14o"W ('IT008 and lTO12). CTD/transmissometer profiles were routinely performed three times a day, roughly at dawn, noon, and just prior to sunset. Additionally, 'die1 experiment' days of intensive profiling (every 3 h) were conducted twice during lTUO8 and three times during TTO12. The beam attenuation profiles clearly show a die1 cycle, with morning lows and evening highs. Transforming the beam c data into suspended particle concentration, and then integrating the particle load to the 1% and 0.1% light depths for each day yields the die1 change in the particle load. Apart from changes in scattering and effective cross section, the die1 change in the integrated particle load (IPL) represents the cycling of mass into and out of the small particle pool. The daytime increase in the integrated particle load (AIPL, defined as the IPL from the evening profile minus the IPL from the morning profile) was converted to carbon units by assuming a 0.4 particulate organic carbon (POC) to particulate matter concentration (PMC) ratio. Our estimate of the net daily POC increase to the 1% light level averaged over the TlBO8 cruise was 26 mmol C m -' day-' (n = 7, SD = 7) and 41 mmol m -' day-' (n = 15, SD = 13) for TTo12. The integration of the 0.1% light level was 29 mmol mm2 day-i during 'lTOO8, and 41 mmol mm2 day-' for lTO12. As the optical method in situ includes the effects of growth, respiration, mixing, settling, grazing and aggregation, our data are not directly comparable to 14C uptake-based primary production measurements. Rather, the difference between the optical estimates of the change in the particle pool and primary production estimates can be ascribed to removal processes in sifu, primarily grazing and aggregation.

[1]  M. Lesser,et al.  Irradiance-induced variability in light scatter from marine phytoplankton in culture , 1993 .

[2]  Timothy C. Granata,et al.  The effect of temporal undersampling on primary production estimates , 1994 .

[3]  Michael J. McPhaden,et al.  TOGA-TAO and the 1991–93 El Niño Southern Oscillation Event , 1993 .

[4]  Michael P. Lesser,et al.  Some changes in the optical properties of marine phytoplankton in response to high light intensity , 1990, Defense, Security, and Sensing.

[5]  T. Dickey,et al.  The emergence of concurrent high‐resolution physical and bio‐optical measurements in the upper ocean and their applications , 1991 .

[6]  T. Platt,et al.  Microplankton productivity in the oligotrophic ocean , 1984, Nature.

[7]  Dariusz Stramski,et al.  Diel variations in the optical properties of a marine diatom , 1993 .

[8]  M. J. Richardson,et al.  Biophysical forcing of particle production and distribution during a spring bloom in the North Atlantic , 1993 .

[9]  R. W. Austin,et al.  The effect of varying phytoplankton concentration on submarine light transmission in the Gulf of California1 , 1974 .

[10]  R. Barber,et al.  Primary productivity and trace-metal contamination measurements from a clean rosette system versus ultra-clean Go-Flo bottles , 1995 .

[11]  B. Osborne,et al.  Light and Photosynthesis in Aquatic Ecosystems. , 1985 .

[12]  M. Hamilton,et al.  Diel variations of bio-optical properties in the Sargasso Sea , 1990, Defense, Security, and Sensing.

[13]  R. Feely,et al.  EqPac: A Process Study in the Central Equatorial Pacific , 1992 .

[14]  L. Prieur,et al.  Absorption by dissolved organic matter of the sea (yellow substance) in the UV and visible domains1 , 1981 .

[15]  Dale A. Kiefer,et al.  Meridional variations in the concentration of chlorophyll and microparticles in the North Pacific Ocean , 1988 .

[16]  Tommy D. Dickey,et al.  Optical determination of particulate abundance and production variations in the oligotrophic ocean , 1989 .

[17]  Curtiss O. Davis,et al.  Photosynthetic characteristics and estimated growth rates indicate grazing is the proximate control of primary production in the equatorial Pacific , 1992 .

[18]  R. Bidigare,et al.  Seasonal variability of bio-optical and physical properties in the Sargasso sea , 1993 .

[19]  R. Olson,et al.  Pigments, size, and distributions of Synechococcus in the North Atlantic and Pacific Oceans , 1990 .

[20]  Howard R. Gordon,et al.  Introduction To Ocean Optics , 1980, Other Conferences.

[21]  T. Dickey,et al.  Variability of bio‐optical properties of the upper ocean associated with diel cycles in phytoplankton population , 1992 .