·
Various
satellite time series were used to evaluate the large-scale space-time
variability in the North Pacific.
·
As shown by
several authors (Esaias et al. 1999; Behrenfeld et al., 2005) one way to
differentiate between various oceanographic provinces is to use the standard
deviation of surface chlorophyll. Different levels of variability tend to
characterize functionally different oceanic regions.

·
Fig. 1. Standard
deviation of the merged (OCTS-SeaWiFS-MODIS-Aqua) monthly Chl time series. Different
oceanographic regions such as the oligotrophic gyres (blue), highly variable
upwelling or seasonal production cycle areas (red) and intermediate variability
areas (green to yellow) are evident. By thresholding the standard deviation
value we can create coarse masks for different oceanographic regions.

·
Fig. 2. One
possible partition of the North Pacific into five different regions according
to their surface Chl variability. The smaller separate patches may be treated
separately or merged with their large neighboring areas.
·
Another way to
find characteristic spatio-temporal domains is to use the EOF analysis. First,
monthly anomalies were created for the merged Chl time series and then EOF
analysis was applied to the monthly anomalies. The following figure shows the
results.

·
Fig. 3. First
principal component of the monthly Chl anomalies time series in North Pacific. Yellow
and red show positive values and blue show negative areas. The patterns on this
image are quite different from the standard deviation patterns of Fig. 1. For
example, while the Bering Sea and the

·
Fig. 4. The temporal
evolution of the first principal component (EOF1) shows close resemblance with
the Extratropical Northern Oscillation index (NOI, Schwing et al., 2002). Note the strong El Nino event of 1997-1998,
and the weak events of 2003 and 2005 corresponding to the minima.
·
The previous
area of interest covered the whole Northern Pacific. We now concentrate on the
eastern North Pacific.

·
Fig. 5. Chlorophyll
anomaly during the height of the 1997/1998 El Niño. Red shows significant
positive anomalies and blue shoes significant negative anomalies. The increased
chlorophyll-a concentration off
·
We now apply EOF
analysis on Chl anomalies in the eastern North Pacific. The results are very
similar to the EOF analysis as applied to the whole North Pacific.

·
Fig. 6. First
principal component of the monthly Chl anomalies time series in eastern North
Pacific. Green to yellow to red show positive values and blue to purple show
negative areas. Positive values in this
mode mean decreased Chl and negative values mean increased Chl during El Niño. These patterns are very similar to patterns in
Fig. 3 but show more detail in Eastern Pacific. For example, we see that the
near-shore zone of Baja California behaves differently from offshore Baja
(first noted in Kahru and Mitchell, 2000). The increased Chl during El Niño
occurs only offshore while the near-shore Chl is suppressed.
·
We now select the
following characteristics areas (masks) according to PC1 of Chl anomalies in
Fig. 3 in order to show time series of Chl in these characteristic domains:
o
1. The northern part of the oligotrophic gyre
(orange)
o
2.
o
3.
o
4.

·
Fig. 7. Selected
characteristics areas (masks) according to PC1 of Chl anomalies in Fig. 3.
·
Time series of
export flux (EF) in these 4 contrasting areas shows opposite response to El
Nino. While areas 1 and 3 have increased net production (NPP) and EF during the
El Nino, areas 2 and 4 have suppressed NPP and EF. It is interesting that the
nearby areas off

·
Fig. 5. Export
flux in the 4 areas (see above) calculated from satellite detected Chl, SST and
PAR and using the VGPM model of Behrenfeld and Falkowski (1997) and the export
flux model of Laws (2004). As predicted by the selection of the areas according
to their contrasting PC1 values, they show opposite responses to El Nino. While
El Nino suppresses Chl, NPP and EF off the
References
Behrenfeld,
M.J., and P.G. Falkowski. 1997. Photosynthetic rates derived from
satellite-based chlorophyll concentration. Limnol. Oceanogr. 42: 1-20.
Behrenfeld,
M.J., E. Boss, D.A. Siegel, D.M. Shea, Carbon-based ocean productivity and
phytoplankton physiology from space, Global Biogeochemical Cycles, 19, GB1006,
doi:10.1029/2004GB002299, 2005.
Esaias
W.E., R.L. Iverson, K.Turpie, Ocean province classification using ocean colour
data: Observing biological signatures of vaiation in physical dynamics, Global Change
Biol., 6, 39-55, 1999.
Kahru,
M., Mitchell, B.G., Influence of the 1997-98 El Niño on the surface chlorophyll
in the
Kahru,
M., B.G. Mitchell, Influence of the El Niño – La Niña cycle on
satellite-derived primary production in the
Laws, E.A. 2004. Export flux and
stability as regulators of community composition in pelagic marine biological communities: Implications for
regime shifts. Prog. Oceanogr. 60: 343-354.
Schwing,
F.B., Murphree, T., Green, P.M., The Northern Oscillation Index (NOI): a new
climate index for the northeast Pacific. Progress in Oceanography, 53, 115-139,
2002.