The North Atlantic Spring Phytoplankton Bloom and Sverdrup's Critical Depth Hypothesis

More than 50 years ago, Harald Sverdrup developed a simple model for the necessary conditions leading to the spring bloom of phytoplankton. Although this model has been used extensively across a variety of aquatic ecosystems, its application requires knowledge of community compensation irradiance (I C), the light level where photosynthetic and ecosystem community loss processes balance. However, reported I C values have varied by an order of magnitude. Here, I C estimates are determined using satellite and hydrographic data sets consistent with the assumptions in Sverdrup's 1953 critical depth hypothesis. Retrieved values of I C are approximately uniform throughout much of the North Atlantic with a mean value of 1.3 mol photons meter−2 day−1. These community-basedI C determinations are roughly twice typical values found for phytoplankton alone indicating that phytoplankton account for approximately one-half of community ecosystem losses. This work also suggests that important aspects of heterotrophic community dynamics can be assessed using satellite observations.

[1]  W. Esaias,et al.  Annual cycles of phytoplankton chlorophyll concentrations in the global ocean: A satellite view , 1993 .

[2]  A. Obata,et al.  Global verification of critical depth theory for phytoplankton bloom with climatological in situ temperature and satellite ocean color data , 1996 .

[3]  K. Banse,et al.  Seasonality of coastal zone color scanner phytoplankton pigment in the offshore oceans , 1994 .

[4]  V. Smetácek,et al.  Spring bloom initiation and Sverdrup's critical‐depth model , 1990 .

[5]  C. McClain,et al.  An investigation of Ekman upwelling in the North Atlantic , 1993 .

[6]  M. Follows,et al.  Interannual variability of phytoplankton abundances in the North Atlantic , 2001 .

[7]  H. Ducklow,et al.  Introduction to the JGOFS North Atlantic bloom experiment , 1993 .

[8]  B. Planque,et al.  Calanus and environment in the eastern North Atlantic. 2. Role of the North Atlantic Oscillation on Calanus finmarchicus and C. helgolandicus , 1996 .

[9]  H. Sverdrup,et al.  On Conditions for the Vernal Blooming of Phytoplankton , 1953 .

[10]  L. Iversen,et al.  Diurnal rhythm in rat pineal cyclic nucleotide phosphodiesterase activity , 1976, Nature.

[11]  A. Morel Optical modeling of the upper ocean in relation to its biogenous matter content (case I waters) , 1988 .

[12]  C. Langdon On the causes of interspecific differences in the growth-irradiance relationship for phytoplankton. II. A general review , 1988 .

[13]  Janet K. Thompson,et al.  Does the Sverdrup critical depth model explain bloom dynamics in estuaries , 1998 .

[14]  D. M. Nelson,et al.  Sverdrup revisited: Critical depths, maximum chlorophyll levels, and the control of Southern Ocean productivity by the irradiance‐mixing regime , 1991 .

[15]  James V. Gardner,et al.  Mapping U.S. continental shelves , 1998 .

[16]  M. Follows,et al.  The Ekman transfer of nutrients and maintenance of new production over the North Atlantic , 1998 .

[17]  James A. Carton,et al.  A Simple Ocean Data Assimilation Analysis of the Global Upper Ocean 1950–95. Part I: Methodology , 2000 .

[18]  W.W.C. Gieskes,et al.  The phytoplankton spring bloom in Dutch coaqtal waters of the North Sea , 1975 .

[19]  M. Follows,et al.  Estimating the convective supply of nitrate and implied variability in export production over the North Atlantic , 2000 .

[20]  Christopher B. Field,et al.  Biospheric Primary Production During an ENSO Transition , 2001, Science.

[21]  James B. Brown,et al.  Physical and biological processes in the North Atlantic during the first GARP Global Experiment , 1990 .

[22]  S. Doney Major challenges confronting marine biogeochemical modeling , 1999 .

[23]  K. Baker,et al.  Meridional variations of the springtime phytoplankton community in the Sargasso Sea , 1990 .