SIBER SPIS sept 2011.pdf - IMBER
SIBER SPIS sept 2011.pdf - IMBER
SIBER SPIS sept 2011.pdf - IMBER
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<strong>SIBER</strong><br />
Science Plan and Implementation Strategy<br />
a more concerted effort to specifically apply the insight these products can provide to the<br />
IO must be targeted. Basic characterization of the typical seasonal cycles of ecological and<br />
biogeochemical processes in equatorial waters is critical, particularly as a comparative baseline<br />
for determining how the annual variability is altered on intra- and interannual timescales (i.e.<br />
by MJO and IOD). These analyses can potentially be augmented by India’s OCM (Ocean<br />
Color Monitor) sensors on Oceansat-1 and 2 and by ESA’s MERIS sensor.<br />
Ocean color measurements have also been used in studies of regional and basinwide biological<br />
response to climate change (Goes et al., 2005; Gregg et al., 2005). Additional studies along<br />
these lines should be motivated. Presumably, climate change is differentially impacting the<br />
sub-basins of the IO; e.g. what regions of the IO are warming fastest, and how are chlorophyll<br />
concentrations and productivity responding to these changes At some level, retrospective<br />
remote sensing studies can also be focused on anthropogenic impacts in coastal waters,<br />
e.g. true color imagery can be used to characterize long-term trends in terrigenous inputs to<br />
coastal zones around the IO rim (e.g. Fig. 4, r i g h t p a n e l). In addition to chlorophyll, standard<br />
ocean color products provided by the NASA-Goddard DAAC such as diffuse attenuation,<br />
CDOM, POC and FLH (fluorescence line height) can be employed to investigate interannual<br />
to interdecadal variation in these properties that can be of particular relevance for coastal<br />
regions impacted by riverine influence.<br />
Satellite ocean color data (SeaWiFS, MODIS-Aqua and OCM) have already revealed striking<br />
contrasts in the chlorophyll distributions and seasonal cycles between the AS and the BoB<br />
(Lévy et al., 2007; Wiggert et al., 2006). However, specific comparative remote sensing<br />
studies that focus on the differences in the ocean color variability between the AS and the<br />
BoB have not been undertaken. Satellite SST, SSH and SSS measurements can/should be<br />
similarly analyzed focusing on differences in the physical variability (upwelling, filaments,<br />
eddy structures, etc.) between the two regions. Combining ocean color, SST and SSH<br />
remote sensing measurements provides potential means to study, for example, differences<br />
in upwelling signatures between the AS and the BoB, e.g. it may be possible to “see” and<br />
characterize cryptic upwelling variability in the BoB because upwelling and eddies that do not<br />
outcrop at the surface should have a strong signature in SSH but a weak signal in SST and<br />
ocean color. Remote SSS measurements can also be combined with ocean color, SST and<br />
SSH to study differences in the freshwater inputs and sea surface density variability between<br />
the AS and the BoB and how this impacts biological response. Satellite remote sensing can<br />
also be gainfully applied to study atmospheric transport, i.e. transport of dust during the SWM<br />
and anthropogenic pollutants particularly during the NEM.<br />
Atmospheric correction problems are still a significant issue for ocean color measurements,<br />
especially in the northern AS where SWM-period aeolian dust loadings are a particular concern<br />
(Banzon et al., 2004). Efforts need to be made to develop better atmospheric correction<br />
algorithms that are specific to the IO.<br />
Although it is not possible to directly detect and survey protozoan, metazoan and higher trophic<br />
level species using satellites, remote sensing can provide useful data. Satellite-derived SST<br />
data can be used to define thermal regimes for micro- and mesozooplankton species. Ocean<br />
color data are particularly useful because they provide the means to map phytoplankton<br />
distributions, i.e. the food source of zooplankton. In general, zooplankton biomass increases in<br />
proportion to phytoplankton biomass, and zooplankton composition may, with study, be found<br />
to vary with chlorophyll concentration in predictable ways. This linkage between phytoplankton<br />
and zooplankton (and often also larval fish) is particularly well defined in strongly advective<br />
regimes, e.g. in filaments where coastal water with high chlorophyll concentration is rapidly<br />
advected offshore and in eddies (e.g. Logerwell and Smith, 2001). Satellites should, in particular,<br />
be employed in combination with in situ process studies that seek to define relationships<br />
between food web parameters and large-scale physical and biological (chlorophyll) patterns.<br />
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