Working Group Members: Dick Barber , Jim Bishop, Mary-Elena Carr, Francisco Chavez , Ellen Druffel, Dick Feely, Dave Karl, Tony Michaels, Jim Murray, Paul Robbins
We seek to identify dominant uncertainties in our knowledge of the variability of carbon fluxes in the Pacific Ocean on seasonal, decadal and centennial time scales, and to determine what effort will yield the greatest reduction in these uncertainties. The most clearly defined time scales of physical variability in the Pacific basin are ENSO (3 - 7 y) and PDO (~30 y). The goal is to understand how these natural variations and those associated with anthropogenic effects influence the structure and dynamics of biogeochemical cycles and carbon fluxes between the ocean and atmosphere.
The enormous increase in our knowledge of oceanographic processes in the Pacific Ocean over the past decade has documented large temporal variations in the carbon cycle. For example, chlorophyll concentration in the Equatorial Pacific underwent factor of 20 changes associated with the 1997-1998 El Niño and subsequent recovery to La Nina conditions. The ecosystem in this region is now believed to shift states abruptly depending on the availability of iron. Studies at the subtropical Pacific time-series station suggest the food web dynamics and productivity in this location shifted to one strongly influenced by nitrogen fixation and phosphorus limitation sometime in the 1980s. SeaWifs ocean color observations from 1997 and 1998 show the presence of meso-scale coccolithophore blooms in the Bearing sea that were never noted in older Coastal Zone Color Scanner data (1978-1986). Forcings that control these changes and the mechanisms that link them to carbon fluxes must be understood and incorporated into basin-scale coupled biological and physical models to accurately predict the response to natural and anthropogenically induced variability.
The questions listed below have all grown out of the synthesis of
existing data and summarize our view of the most important unknowns
in the processes that control variability in Pacific Ocean carbon
fluxes.
Nitrogen fixation creates reactive nitrogen which is then available to the rest of the life in the sea. Denitrification removes this reactive nitrogen as part of the metabolism of a specific group of micro-organisms. The balance of these two processes controls the total pool of reactive nitrogen, primarily nitrate, in the ocean. The Pacific Ocean contains one of the largest areas of water column and sediment denitrification in the world. Nitrogen fixation is widespread over the oligotrophic surface waters of the Pacific and apparently fluctuates on interannual and decadal time-scales, although the absolute rates over the whole basin are unclear. The creation of reactive nitrogen by diazotrophs will result in the net uptake of atmospheric CO2, and denitrification will cause the return of CO2 to the atmosphere, modulated by the residence time of the nitrate in the ocean. If these two rates are exactly in balance, the net exchange of CO2 with the atmosphere will be zero; imbalances between these two rates will result in a net ocean uptake or outgassing of CO2.
The nitrogen fixation-denitrification balance has the potential to
have an effect on the concentration of carbon in the atmosphere.
Current estimates of the global denitrification rate are over 300
Tg/y, and Pacific rates may be greater than half of this total.
Estimates of the global rates of nitrogen fixation are only about 100
Tg/y, again with approximately half of this in the Pacific Ocean.
Given these estimates, either the ocean is wildly out of balance or
one or both of the rates is in error. An imbalance implies a
concomitant trend in atmospheric CO2 change. Ice core data
indicate that since about 8000 years before the industrial revolution
the atmospheric pCO2 increased slowly by about 20 ppm. One
of the goals of nitrogen cycle studies is to determine its role in
the air-sea partitioning and variability in atmospheric
CO2.
Observations of nitrate draw-down, 14C primary
productivity and 15N uptake incubation experiments in the
Canadian and Japanese JGOFS time-series sites indicate that the rates
of carbon export and new production in the western subarctic Pacific
are about twice that of the eastern part of this basin. The reasons
for this difference are unknown given that both sides of this basin
are nutrient replete, year-round. Since the western subarctic Pacific
has been identified by global surface CO2 maps as one of
the important regions of net CO2 flux into the oceans, an
investigation into the reasons for this asymmetry is warranted. Key
possibilities for the difference are: (1) differences in Fe flux
between the eastern and the western basin because of prevailing wind
patterns; (2) physical processes of seasonal mixed layer deepening
and mechanisms controlling exchange between the euphotic zone and
nutrient-enriched upper thermocline; and (3) hydrological cycle
differences in the two basins with emphasis on the influence of
freshwater input to the upper ocean on physical mixing processes. To
understand the effect of natural decadal-scale oscillations and
anthropogenically-induced climate changes on the rates of physically
and biologically induced CO2 exchanges, one must know the
importance of these mechanisms in the subarctic Pacific
ocean.
Many lines of evidence exist that show past variability in the
ventilation of the upper ocean on interannual to decadal time scales.
For example decadal variability of the climate mean state shift
occurred abruptly in 1976. After this time, more frequent, severe El
Niño events occurred. These changes in the climate mean state
are associated with large variability of the wind field and regional
heat storage in the upper ocean. This significant variation from year
to year in the ventilation of the Pacific waters is large and likely
affects carbon fluxes in profound ways. Local manifestations of the
decadal shifts likely include changes in mixing, convection, gas
exchange and upwelling. All would contribute to the changes in the
solubility pump. Further, each has an impact on nutrient supply and
productivity leading to changes in the biological pump. Given the
grand size of the North Pacific basin, interannual (ENSO) and decadal
(PDO) scale variability in ventilation is likely important in upper
ocean control of atmospheric pCO2. Whether recent changes
are a result of global warming or natural variability due to
atmospheric forcing or interactions between circulation in the
tropical and extratropical Pacific can be resolved with a combination
of paleoceanographic and instrumental data. A boost in the number and
location of moorings and/or the use of drifters or ships of
opportunity are strategies to be considered for increasing spatial
and temporal instrumental data coverage.
Margin processes are not marginal in the context of global carbon cycling on decadal to centennial time scales. Continental margins provide Fe both to the overlying water and to the open ocean, are sites of a major portion of global denitrification, and are the gateway for terrestrial carbon input to the ocean. Primary productivity measurements, from S. California, central California, and the Washington margin indicate strong seasonality in primary productivity, and average values are >100 mmolC/m2d. New production is on the order of 50 mmolC/m2d which is 10 times greater than new production at BATS, HOT and Sta. P and 7 times greater than new production in the Equatorial Pacific (JGOFS EqPac). Margins represent approximately 10% of the area of ocean basins, hence global new production should be about evenly divided between the margins and the open ocean.
Important reasons to study continental margins in carbon cycle
research are mainly their role in carbon export and preservation and
their susceptibility to anthropogenic perturbations. Variability in
the recycling of exported carbon and its remineralization length
scales should affect global CO2 budgets on decadal to
centennial time scales. Carbon burial in margin environments is a
much more important removal term than burial in the deep ocean
because of the high flux and relatively shallow water column. Burial
rates on river-dominated and narrow margins are not well documented.
Organic mater preservation rates in margin areas are subject to large
variations in time and space because of physical (floods, coastal
erosion) and anthropogenic (eutrophication) forcing. Margins are
particularly sensitive to anthropogenic perturbations (trawling,
pollution, coastal building) and many elements of coastal ecosystems
have been documented to track changes in physical forcing (PDO,
ENSO).
Iron is now considered to play a crucial role in oceanic nutrient
cycles. It may control the biological activity in high-nutrient, low
chlorophyll areas like the North Pacific, Equatorial Pacific and the
Southern Ocean. It may also control the rate of nitrogen fixation in
the oligotrophic gyres. Both of these processes may influence the
air-sea partitioning of CO2, and they determine the
ecosystem structure of these basins. The sources of iron are much
more diverse than previously thought, and an understanding of each is
required to determine the overall controls on biogeochemistry. In
open ocean areas, atmospheric deposition of dust is the primary
source of iron. These fluxes are closely tied to terrestrial sources
and their dynamics and tend to decline with distance from the source.
Upwelling of subsurface, regenerated iron is important in areas where
the primary macronutrients are brought up from below. This cycle
operates in rough concert with the macronutrient cycles. Near land,
margin sediments are a third source of iron, both as a dissolved flux
and a particulate, resuspended flux. As iron is mobilized from
sediments, it spreads into the interior and becomes available through
upwelling. Finally, active volcanoes emit large amounts of iron and
phosphate and could be local airborne sources.
Upwelling of waters enriched in nutrients and carbon dioxide creates a tongue of cold surface water along the equator, from the coast of South America to the international dateline in the equatorial Pacific Ocean. The vast area involved makes this region the largest natural oceanic source of atmospheric CO2. Physical processes and biological production determine the strength of this source. During normal or cool conditions, high concentrations of nitrate in the equatorial Pacific lead to unexpectedly small increases in chlorophyll. This low productivity contributes directly to the loss of upwelled CO2 to the atmosphere. Small-scale iron fertilization experiments have shown that the low productivity can result from iron limitation. The upwelled water originates from the EUC, which flows eastward across the basin at a depth of 20 to 200m and is enriched in iron.
Every 3 to 7 years the central and eastern equatorial Pacific
warms dramatically as El Niño develops. On decadal scales the
Pacific Decadal Oscillation (PDO) is an important source of
variability. Early conceptual models suggested that during El
Niño, Kelvin waves were the primary agents affecting
biological productivity, since upwelling-favorable winds were
maintained in the eastern Pacific. The waters upwelled were low in
nutrients and degassing of CO2 to the atmosphere, and
productivity was hence reduced. During weak to moderate events, zonal
wind anomalies are restricted to the western Pacific. However, during
the strong 1997-98 event the zonal wind anomalies extended into the
eastern equatorial Pacific, shutting down local upwelling and
degassing of CO2 to the atmosphere in the central
equatorial Pacific for several months. After recovery from the
1997-98 El Niño the equatorial Pacific again became a source
of CO2 to the atmosphere and an unprecedented large bloom
was observed, presumably the result of an enhanced supply of iron.
While most think that the equatorial Pacific air-sea flux of
CO2 is physically driven, the role of the biological pump
has yet to be adequately resolved for both particulate and dissolved
organic carbon and particulate inorganic carbon. Further, the
available field data is from the warm phase of the PDO. How the
equatorial Pacific will respond to the projected cool phase of the
PDO or to global warming is uncertain.
Organic matter respiration below the sun-lit surface ocean is a dominant factor controlling chemical transformations and biological communities of the subsurface ocean. The rate of respiration and downward transport of organic material (both particulate and dissolved) influence the depth scales of the chemical and biological changes, which determines the response time of sequestration of carbon in the ocean by the biological pump and ocean circulation. Tracers in the euphotic zone (including 13C, the three oxygen isotopes, and N isotopes) can make a big impact on our understanding of production rates and hence also export processes. Rates of respiration in the sub-euphotic zone have been determined by modeling apparent oxygen utilization and transient and short-lived tracers, because they are too slow to measure directly in most cases. A more complete understanding of the rates of respiration and transport processes will help oceanographers determine the response time of the carbon cycle to climate change, should help close the mass balance inferred from upper ocean tracers, and bear on questions of spatial variability of inputs. A better understanding of these processes will also aid in our attempt to use tracers of metabolic processes as indicators of decadal scale changes in the strength of the carbon pump. Specific areas that are ripe for improved understanding are: (1) the rates and mechanisms of particulate and dissolved organic matter degradation, including the differing rates of remineralization of micronutrients, P, N, and C; (2) the rates and mechanisms of particulate inorganic carbon (PIC) production and dissolution; (3) rates of mixing and subduction in the upper ocean, and (4) the influence of different amounts and types of organic mater ballast (in the form of calcium carbonate and opal) on its sinking and degradation characteristics.