Chlorofluorocarbons
Ocean distributions of anthropogenic transient tracers, such as
chlorofluorocarbons (CFCs) and radiocarbon (14C) reveal pathways, rates
and mechanisms of ocean circulation and mixing. CFC-11 is entirely man-made,
and its concentration in the atmosphere increased rapidly from the 1930s
to the 1990s. It is soluble and has been invading the oceans, marking
waters which have recently been near the surface. Here you can see an animation of the invasion of CFC-11 into the
deep North Atlantic in a one-degree resolution configuration of the
MIT ocean circulation model.
The Carbon cycle
Understanding
the circulation and CO2 biogeochemistry of the oceans is key to our
ability to understand past climates and assess the future evolution of climate.
The ocean is important in the regulation of heat and moisture fluxes, and
oceanic physical and biogeochemical processes are major regulators of natural
atmospheric carbon dioxide (as well as being an important sink of fossil fuel CO2).
The physics, chemistry and biology of the ocean are coupled since the oceanic CO2
cycle is controlled by the ocean circulation, the supply of sunlight, and major
and trace nutrients delivered by the oceanic and atmospheric circulations.
Interannual Variability of Air-Sea Carbon and Oxygen Fluxes
How do changes in ocean circulation and mixing on interannual timescales affect
the air-sea exchange of trace gases, such as carbon dioxide and oxygen? We
use numerical models of ocean circulation and biogeochemistry to examine the
possible effect of interannual changes in meteorological forcing and upper
ocean circulation on the fluxes of carbon dioxide and oxygen between the
ocean and atmosphere.
With former graduate student Galen McKinley, using global ocean circulation
estimates from the ECCO consortium we
estimated the interannual variability in the global air-sea exchange of
carbon dioxide.
The time-mean air-sea flux of carbon dioxide from a global, interannually
varying simulation made by Galen McKinley. The ocean model absorbs
carbon from the atmosphere in regions of sea surface heat loss and
biological uptake of carbon (e.g. North Atlantic). The ocean model is losing
carbon dioxide from the ocean in regions where carbon rich deep waters
upwell to the surface (e.g. Tropical Pacific).
Interannual variability in the global flux of carbon dioxide across the
model's sea surface is dominated by the role of changes in the Tropical
Pacific associated with El Nino. In that region the model's predicted
fluxes show general agreement with inferences from observed data
and atmospheric inverse models. The ocean model suggests little role
for the subtropical and subpolar oceans in modulating atmospheric CO2
on
inter-annual timescales in contrast with inferences from atmospheric inverse
models. This apparent disagreement is an outstanding scientific question
which remains to be resolved. What is the role of the extra-tropical oceans
in modulating atmospheric CO2 on interannual timescales?
Interannual Variability of the North Atlantic Spring Bloom
In collaboration with Dr. Stephanie Dutkiewicz we have examined
the relationships between regional and interannual
variations in meteorological forcing and the variability of the spring
bloom of biological productivity in the North Atlantic ocean using
remotely sensed ocean color data from SeaWiFs mission.
An animation, showing the seasonal and interannual variability of the
North Atlantic spring bloom, as observed from space by SeaWiFS, can be
seen here
(1.9Mb animated gif, images produced by Stephanie Dutkiewicz). Monthly
images are sequenced, for the two years 1998 and 1999.
We have also demonstrated the relationship between meteorological forcing
and the bloom response in a numerical model of the time dependent ocean
circulation with a highly simplified representation of the ecosystem
of the North Atlantic (a collaboration with Dr. Watson Gregg of NASA/Goddard Space Flight Center).
Modeling the Ocean Iron Cycle
With former graduate student Payal Parekh and Prof. Ed Boyle at
MIT, we have developed an explicit parameterization of the iron cycle
in the global ocean. Iron is supplied to the remote ocean by Aeolian
(wind-borne) dust deposition.
Biological processes in the upper ocean utilize iron and other nutrients,
including nitrate and phosphate, creating organic matter some of which
eventually sinks into the deep ocean where it is remineralized.
In the ocean interior iron it is scavenged onto sinking particles and
can become bound to an organic ligand, or complexed though neither of
these processes happens to nitrogen or phosphorus. Hence iron is decoupled
from the macro-nutrients. In many upwelling regions there is insufficient iron available to utilize all of the
available macro-nutrients. Hence, it
is thought that iron limits the efficiency of the biological storage of
carbon in the oceans.
In the framework of a coarse resolution ocean model we explicitly account
for the iron limitation in remote ocean regions. The figure illustrates
the modeled dissolved iron distribution (nM) at the surface and 1000m.
The distributions are generally consistent with the available, but very
sparse, observations.
The low surface iron concentrations in the Southern Ocean limit biological
production and export.
In collaboration with Stephanie Dutkiewicz, we have coupled the iron
model to an ecosystem model which resolves two functional groups
of phytoplankton and explicitly represents the cycles of the limiting
nutrients phosphorus, silica, iron and light. This is again in a
coarse resolution framework. Here we compare the mean surface
chlorophyll as observed by the SeaWiFS remote instrument and from
the numerical model.
Ocean Carbon-Cycle Model Intercomparison Project (OCMIP)
Comparing model simulations of ocean tracers with observed data can
inform us about the tracer transport circulation of our models.
We have taken participated in the Ocean Carbon Model Intercomparison Project,
OCMIP in which
a number of numerical global ocean circulation models are used to simulate
a suite of ocean tracers. Comparisons show significant differences between
models and data, and between the different models.
For the OCMIP study we used a coarse-resolution configuration of the
MIT ocean circulation model (2.8 degree horizontal resolution, 15 vertical
levels).