The Global Carbon Cycle: A Test of Our Knowledge of Earth as a System Author(s): P. Falkowski, R. J. Scholes, E. Boyle, J. Canadell, D. Canfield, J. Elser, N. Gruber, K. Hibbard, P. Högberg, S. Linder, F. T. Mackenzie, B. Moore III, T. Pedersen, Y. Rosenthal, S. Seitzinger, V. Smetacek, W. Steffen Source: Science, New Series, Vol. 290, No. 5490 (Oct. 13, 2000), pp. 291-296 Published by: American Association for the Advancement of Science Stable URL: http://www.jstor.org/stable/3078125 Accessed: 08/01/2010 16:49 Your use of the JSTOR archive indicates your acceptance of JSTOR's Terms and Conditions of Use, available at http://www.jstor.org/page/info/about/policies/terms.jsp. JSTOR's Terms and Conditions of Use provides, in part, that unless you have obtained prior permission, you may not download an entire issue of a journal or multiple copies of articles, and you may use content in the JSTOR archive only for your personal, non-commercial use. Please contact the publisher regarding any further use of this work. Publisher contact information may be obtained at http://www.jstor.org/action/showPublisher?publisherCode=aaas. Each copy of any part of a JSTOR transmission must contain the same copyright notice that appears on the screen or printed page of such transmission. JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. American Association for the Advancement of Science is collaborating with JSTOR to digitize, preserve and extend access to Science. http://www.jstor.org REVIEW: CLIMATE The CHANGE Global Carbon Knowledge of Cycle: Earth A as Test a of Our System P. Falkowski,'*t R. J. Scholes,2* E. Boyle,3t J. Canadell,4t D. Canfield,5t J. Elser,6t N. Gruber,:t K. Hibbard,8: P. Hogberg,9t S. Linder,'?t F. T. Mackenzie,"1 B. Moore 111,8:T. Pedersen,'2t Y. Rosenthal,1 S. Seitzinger,': V. Smetacek,'13 W. Steffen'4: over the past 420,000 years, the climate system has operated within a relatively conMotivated by the rapid increase in atmospheric CO2due to human activities since the strained domain of atmospheric CO2 and IndustrialRevolution,several international scientific research programshave analyzed the role of individualcomponents of the Earthsystem in the global carbon cycle. Our temperature(7, 8) (Fig. 1). In the CO2-temknowledge of the carbon cycle within the oceans, terrestrial ecosystems, and the peraturephase space that characterizedthe atmosphere is sufficiently extensive to permit us to conclude that although natural preindustrial world, CO2 oscillated in processes can potentially slow the rate of increase in atmospheric COz, there is no 100,000-year cycles by approximately 100 natural "savior"waiting to assimilate all the anthropogenically produced CO2 in the partsper million by volume (ppmv), between coming century. Our knowledge is insufficient to describe the interactions between about 180 and 280 ppmv. On millennial time the components of the Earthsystem and the relationship between the carbon cycle scales, changes in CO2 recordedin ice cores and other biogeochemical and climatological processes. Overcoming this limitation are highly correlatedwith changes in temperrequires a systems approach. ature (9). Although high-resolution analysis of ice cores suggests that there are periods in Earth'shistory when temperaturecan change ver the past 200 years, human activ- generations. Given present trends in energy relatively sharply without a discernible ities have altered the global carbon demands,ample fossil fuel reserves, a lack of change in CO2 (7), the converse does not alternative concerted, global, cycle significantly. Understanding energy produc- appearto be true. the consequences of these activities in the tion strategies,andprojectionsof humanpopComparison of the present atmospheric coming decades is critical for formulating ulation growth, atmosphericCO2 concentra- concentrationof CO2with the ice core record tions appearfated to increase throughoutthe reveals that we have left the domain that economic, energy, technology, trade, and security policies that will affect civilization for coming century (1, 2). The rate of change in defined the Earth system for the 420,000 atmosphericCO2depends,however, not only years before the IndustrialRevolution (10) 'Institute of Marineand Coastal Sciences, Rutgers on humanactivities but also on biogeochemi(Fig. 1). Atmospheric CO2 concentrationis University, 71 Dudley Road, New Brunswick,NJ cal and climatological processes and their now nearly 100 ppmv higher, and has risen to 08901, USA.2Councilof Scientificand IndustrialReinteractionswith the carbon cycle. Here we thatlevel at a rateat least 10 andpossibly 100 search,Environmental Division,Post Office Box 395, examine some of the changes in biogeo- times fasterthan at any other time in the past Pretoria0001, SouthAfrica.3Earth,Atmospheric,and PlanetaryScience Department,MassachusettsInsti- chemical and climatological processes con420,000 years. We have driven the Earth tute of Technology,42 CarletonStreet, MailCode: comitant with alterations in the carbon and system from the tightly bounded domain of MA USA. 4Global E34-258,Cambridge, 02142-1324, in nutrient the world, cycles contemporary glacial-interglacial dynamics. Are we in a Change and TerrestrialEcosystems International ProjectOffice, CommonwealthScientificand Indus- and comparethese processes with our under- transitionperiod to a new, stable domain? If trialResearchOrganisationWildlifeand Ecology,Post so, what are the main forcing factors and standing of the preceding 420,000 years of OfficeBox284, Canberra, AustralianCapitalTerritory, Earth's feedbacksof this transition?What will be the history. 2601, Australia.Slnstitute of Biological Sciences, climatological features of a new domain? Odense University,5230 Odense,Denmark.6DepartWhat will be the responses and feedbacks of ment of Zoology,ArizonaState University,Temple, Entering Uncharted Waters AZ 85287-1501, USA.7lnstituteof Geophysicsand Under the auspices of the InternationalGeoEarth's ecosystems? How and when can and PlanetaryPhysics and Departmentof Atmospheric sphere-BiosphereProgramme(IGBP), severshould we returnto the preindustrialdomain? Sciences,5853 SlichterHall,Universityof California, al scientific studies have The active carbon reservoirs and their international large LosAngeles,CA90095-4996, USA.8Institutefor the focused on elucidatingvarious aspects of the strengths. Atmospheric CO2 exchanges rapStudy of Earth,Oceans, Space, Universityof New global carboncycle over the past decade (3). idly with oceans and terrestrialecosystems Hampshire,MorseHall,39 CollegeRoad,Durham,NH 03824, USA.9Departmentof ForestEcology,Swedish These programshave helped addresstwo ma(11). The ratio between the rate at which Universityof AgriculturalSciences,S-901 83 Umea, recurrentquestions in the currentdebate these two reservoirsabsorbatmosphericCO2 Sweden.'Department for ProductionEcology,Swed- jor about andthe rateof emissions determinesthe overglobal change: Can we distinguishbeish Universityof Agricultural Sciences,PostOfficeBox tween anthropogenicperturbationsand natu- all rate of change of atmosphericCO2. The 7042, S750 07 Uppsala,Sweden. "Department of sink strengthof the reservoirsdeterminesthe Oceanography,SOEST,Universityof Hawaii,Honolu- ral variability in biogeochemical cycles and lu, HI,96822, USA.'2Departmentof Earthand Ocean climate? And what is the of to absorb excess or anthropogenic sensitivity capacity Sciences,Universityof BritishColumbia,Vancouver, Earth's climate to changes in atmospheric CO2. During glacial-interglacialtransitions, BCV6T 1Z4, Canada.'3AlfredWegenerInstitutefor CO2? We consider the two questions in the for example, the atmosphereacts to transfer Polar and MarineResearch,Am Handelshafen12, 27570 Bremerhaven,Germany.'41GBPSecretariat, context of the relatively recent geological carbonbetween terrestrialecosystems andthe RoyalSwedishAcademyof Sciences,Box 50005 Lilia history of Earth, for which we have robust oceans. The remarkableconsistency of the Frescativagen4, S-10405 Stockholm,Sweden. paleoclimatologicalproxies. upperand lower limits of the glacial-intergla*Co-chairsof the InternationalGeosphere-Biosphere Arrheniusrecognized over 100 years ago cial atmosphericCO2 concentrations,and the Programme(IGBP)WorkingGroupand lead authors. that atmosphericCO2plays a criticalrole apparentfine control over periods of many tTo whom correspondenceshould be addressed.E- (4) in regulating Earth's temperature (5, 6). thousands of years aroundthose limits, sugmail:[email protected] IMembersof the IGBPWorkingGroup. Analyses of ice cores strongly suggest that gest strong feedbacks that constrainthe sink www.sciencemag.org SCIENCE VOL290 13 OCTOBER 2000 291 SCIENCE'S strengths in both the oceans and terrestrial ecosystems. The relatively rapid transition from glacial to interglacial states and the initially steep, but eventually gradual,transition into glacial periods (8) suggests that the ratesof absorptionand emission of CO2from the oceans and terrestrial ecosystems are asymmetrical.It should be noted thatbecause of this asymmetry, the average atmospheric CO2 concentrationduring the past 420,000 years was only -220 ppmv, not 280 ppmv as usually ascribed (12). How is atmospheric CO2 regulated? The total of dissolved inorganic carbon in the oceans is 50 times that of the atmosphere (Table 1), and on time scales of millennia, the oceans determineatmosphericCO2 concentrations,not vice versa. AtmosphericCO2 continuouslyexchanges with oceanic CO2 at the surface.This exchange, which amountsto -90 gigatons (Gt) of carbonper year in each direction, leads to rapid equilibrationof the atmospherewith the surfacewater.Upon dissolution in water,CO2forms a weak acid that reacts with carbonate anions and water to form bicarbonate.The capacityof the oceanic carbonate system to buffer changes in CO2 concentration is finite and depends on the addition of cations from the relatively slow weatheringof rocks. Because the rate of anthropogenicCO2 emissions is several orders of magnitudegreaterthan the supply of mineral cations, on time scales of millennia the. ability of the surface oceans to absorb CO2 will inevitably decrease as the atmospheric concentrationof the gas increases (13). The concentrationof total dissolved inor- COMPASS ganic carbonin the ocean increasesmarkedly below aboutthe upper300 m, whereit remains significantly above the surface ocean-atmosphere equilibriumvalue in all ocean basins. The higherconcentrationof inorganiccarbonin the ocean interiorresultsfroma combinationof two fundamental processes: the "solubility pump"and "biologicalpumps"(14, 15). The efficiency of the solubility pump depends on the thermohalinecirculationand on latitudinal and seasonal changes in ocean ventilation (16, 17). CO2 is more soluble in cold, saline waters, and sequestrationof atmospheric CO2 in the ocean interioris therefore controlled by the formation of cold, dense water masses at high latitudes, especially in the North Atlantic and in the Southern Ocean confluence. As these water masses sink into the ocean interiorand are transported laterally, CO2 is effectively prevented from re-equilibratingwith the atmosphereby a cap of lighter overlying waters. Re-equilibration occurs only when waters from the ocean interiorare broughtback to the surface, decades to several hundredsof years later. Coupled climate-ocean simulations (6, 18) suggest that CO2-inducedglobal warming will lead to increasedstratificationof the water column. If this occurs, the transportof carbon from the upper ocean to the deep ocean will be reduced, with a resulting decrease in the rate of sequestrationof anthropogenic carbon in the ocean (19, 20). The combined effects of progressive saturationof the buffering capacity and increased stratification will weaken two importantnegative feedbacks in the carbon-climate system, Modern 350- E 3000 =. Qs .O 250- 200 200- 13.U -10 . . . . I . .I -5 .I I. . I ?? 0 Deuterium-based TemperatureAnomalies, ?C Fig. 1. A correlationbetween atmosphericpartial pressureof CO2 (pCO2) and isotopic (8D) temperatureanomaliesas recordedin the Vostokice core.Thefigureshows that climatevariations in the past 420,000 years operatedwithin a relativelyconstraineddomain.Data are from (8). 292 13 OCTOBER 2000 VOL290 therebyreducingthe rateof oceanic uptakeof anthropogenicCO2. The magnitude of these feedbacks is critically dependent on how ocean circulationand mixing will respondto the climatic forcing. Biological processes also contributeto the absorptionof atmosphericCO2 in the ocean. Phytoplanktonphotosynthesislowers the partial pressure of CO2 in the upper ocean and therebypromotesthe absorptionof CO2from the atmosphere. Approximately 25% of the carbonfixed in the upperocean sinks into the interior(21, 22), where it is oxidized through heterotrophicrespiration,raising the concentration of dissolved inorganic carbon (DIC). The export of organic carbon from the surface to the ocean interiorpresently accounts for - 11 to 16 Gt of carbonper year (23). This process keeps atmospheric CO2 concentrations 150 to 200 ppmv lower thanthey would be if all the phytoplanktonin the ocean were to die (23, 24). In addition to the organic biological pump, several phytoplanktonand zooplankton species form CaCO3 shells that sink into the interior of the ocean, where some fraction dissolves. This inorganic carbon cycle leads to a reduction in surface ocean DIC relative to the deep ocean and is therefore sometimes called the "carbonate pump." The process of precipitatingcarbonates, however, increases the partial pressure of CO2 (25). Hence, on time scales of centuries, while the carbonatepump lowers DIC concentrationsin the upperocean, it simultaneously leads to the evasion of CO2 from the ocean to the atmosphere. Coupled climate-biogeochemical models suggest that the biological pumps tend to counteractthe decrease in uptake caused by the solubility pump (20, 26). If the biological pumps are to absorb anthropogenicCO2 in the coming century,their efficiency must increase. In principle,this can be accomplished by any or all of four processes: (i) enhancing utilization of excess nutrients in the upper ocean, (ii) adding one or more nutrientsthat limit primary production, (iii) changing the elemental ratios of the organic matter in the ocean, and (iv) increasingthe organiccarbon/ calcite ratio in the sinking flux (27). There are significant gaps in our knowledge that limit our ability to predict the magnitude of changes in oceanic uptake, but the likely changes in the biological pump are too small to counteractthe projectedCO2 emissions in the coming century. Almost certainly, however, changes in oceanic ecosystem structure will accompany changes in physical circulation (and hence changes in nutrientsupplies), lowered pH, and changes in the hydrological cycle. Our present knowledge of the factors thatdeterminethe abundanceand distribution of key groups of marine organisms is so limited that it is unlikely we will be able to predict such changes within the next decade SCIENCEwww.sciencemag.org SCIENCE'S with reasonable certainty (28). These uncertainties affect our ability to predict specific responses, but not the sign of the changes in atmosphericCO2or the impactof this change on upperocean pH. If our currentunderstanding of the ocean carboncycle is borneout, the sink strengthof the oceans will weaken, leaving a largerfractionof anthropogenicallyproduced CO2 in the atmosphere or to be absorbed by terrestrialecosystems. Terrestrialecosystems also exchange CO2 rapidlywith the atmosphere,but unlike in the oceans, there is no physicochemical pump. CO2 is removed from the atmospherethrough photosynthesis and stored in organic matter. It is returnedto the atmospherevia a number of respiratorypathways that operate on various time scales: (i) autotrophicrespirationby the plants themselves; (ii) heterotrophicrespiration,in which plant-derivedorganic matter is oxidized primarily by soil microbes; and (iii) disturbances,such as fire, in which large amountsof organic matterare oxidized in very short periods of time. On a global basis, terrestrialcarbon storage primarilyoccurs in forests (29). The sum of carbon in living terrestrialbiomass and soils is approximately three times greater thanthe CO2in the atmosphere(Table 1), but the turnovertime of terrestrialcarbon is on the orderof decades. Direct determinationof changes in terrestrial carbon storage has proven extremely difficult (30). Rather, the contributionof terrestrialecosystems to carbon storage is inferred from changes in the concentrations of atmospheric gases, especially CO2 and 02, their isotopic composition, inventories of land use change, and models (31-33). The models requireaccurate knowledge of the oceanic uptakeof CO2 (31, 34, 35). Terrestrialnet primaryproduction (NPP) (36) is not saturatedby present atmospheric CO2 concentrations (37). Consequently, as atmosphericCO2 increases, terrestrialplants are a potential sink for anthropogeniccarbon. The principalcarbon-fixingenzyme in plants is ribulose 1,5-bisphosphatecarboxylase/oxygenase (rubisco) (38). In C3 plants, the activity of rubisco increases with increasing CO2 concentrations,saturatingbetween 800 and 1000 ppmv CO2, a concentration that will probably be reached early in the next century at the present emissions rate (2). Because the saturation function decreases as CO2 increases, terrestrialplants will become less of a sink for CO2 in coming decades. Some experimental evidence suggests that because of nutrientlimitation (39), NPP may level off at only 10 to 20% above current rates, at an atmosphericCO2concentrationof 550 to 650 ppmv, or double preindustrial concentrations (40). Furthermore,increased temperaturewill probably lead to higher microbial heterotrophicrespiration,which may COMPASS counteractand even exceed the enhancement to about 5% of the present anthropogenic of NPP (41). The combined effects of higher CO emissions. There is no evidence that phosphorussigCO2concentrations,highertemperatures,and changes in disturbanceand soil moisture re- nificantly limits primaryproductionin coastgimes lead to considerableuncertaintyabout al or open oceans on a global scale (51) or the ability of terrestrialecosystems to miti- thatphosphorusloading of the coastal oceans gate againstrising CO2in the coming decades has significantly altered global primarypro(42). However, recent results from long-term duction (46). soil warming experiments in a boreal forest Iron is a micronutrientthat limits both contradictthe idea that the projected rise in primaryproduction(52) and nitrogenfixation temperatureis likely to lead to forests that are in many areas of the ocean (53). Eolian now carbon sinks becoming carbon sources (windbome) iron fluxes, a principalsource of in the foreseeable future (43). iron inputto the open ocean, are coupled both to land use and the hydrological cycle (54). Again, as in the case of marine ecosystems, we can predict that the negative feed- Episodic aridity affects eolian iron supplies, back afforded by terrestrial ecosystems in and in the coming decades, iron fluxes to the removing anthropogenic CO2 from atmo- ocean could therefore increase because of sphere will continue; however, the sink increasedevaporationof soil moisture or destrength will almost certainly weaken. The crease because of increased precipitation exact magnitude of the change in sink (55). Increases in evaporationand increases in precipitationare expected in differentparts strengthremains unclear. Interactionof the carbon cycle with other of the land surface in response to increasing biogeochemical cycles. All biotic sinks for global temperatures.Thus, although increasCO2 require other nutrients in addition to ing temperatureand its potentialinfluence on carbon.Humanshave affected virtuallyevery the availabilityof iron in the open ocean will major biogeochemical cycle (Table 2), but affect the biological uptake of carbon in the the effects of these impacts on the interac- ocean, at present we do not know the sign of tions between these elemental cycles are the changes. However, even if iron fluxes were to increase to such an extent that ocepoorly understood (44). The production of synthetic fertilizers, the cultivation of nitro- anic nitrogen fixation were stimulatedto the maximum, the maximum change in atmogen-fixing crops, and the deposition of fossil fuel-associated nitrogen are collectively of spheric CO2that could ensue would be about the same order of magnitude as naturalbio- 40 ppmv. Although not insignificant,such an logical nitrogen fixation (45). These inputs effect is unrealistic on time scales of centuwill continue to rise with the projected in- ries (56). crease in human population (46). Similarly, Eolian nitrogeninputscan also potentially there has been an approximatelyfourfold in- enhanceboth terrestrialand marineuptakeof crease in phosphorusinputs to the biosphere, anthropogenicCO2 (37). In terrestrialecoprimarilydue to mining of phosphoruscomsystems, the sink strengthresulting from eolian nitrogen deposition depends on the carpounds for fertilizer. At first glance, one might conclude that bon: nitrogenratio of the stored organic matsimultaneous increases in nitrogen fixation and phosphate production would stimulate Table 1. Carbonpools in the major reservoirson the biological sequestrationof carbon in ter- Earth. restrial and marine ecosystems. Will such stimulation provide salvation from the conQuantity Pools (Gt) tinued anthropogenicemissions of CO2to the atmosphere? 720 Atmosphere It is estimated that by 2050, the total Oceans 38,400 transport of fixed inorganic nitrogen from Total inorganic 37,400 land to the coastal zone will have increased Surface layer 670 fromthe presentvalue of -20 teragrams(Tg) 36,730 Deep layer Total organic of nitrogen to - 40 Tg of nitrogen per year 1,000 (47), concomitantwith an increase in human Lithosphere >60,000,000 population from 6 to 9 or 10 billion. AlSedimentarycarbonates 15,000,000 Kerogens though nutrientloading has resultedin coastal eutrophicationon a global scale (48), deni- Terrestrialbiosphere (total) 2,000 trification presently removes virtually all 600-1,000 Livingbiomass Dead biomass 1,200 land-derivednitrogen before it can reach the ocean Coastal denitrification 1-2 (49, 50). open Aquatic biosphere thus effectively decouples the terrestrialand Fossil fuels 4,130 Coal 3,510 oceanic nitrogencycles. However, even if no Oil 230 denitrificationoccurred,the increasedflux of Gas 140 land-derived nitrogen would sequester only Other (peat) 250 0.4 Gt of carbonper year (48), corresponding www.sciencemag.org SCIENCE VOL 290 13 OCTOBER2000 293 SCIENCE'S ter and the degree of nitrogen saturationof soils (44, 57-59). Nitrogen deposition is predicted to continue and has the potential to enhance the carbon sink in nitrogen-limited ecosystems, but it will probablybecome decreasingly effective at doing so. Futurenitrogen deposition will largely occur on already nitrogen-saturatedsoils, such as in the forests of WesternEurope,China, and India, and on agriculturallands in the tropics,whose capacity to sequester carbon is intrinsically small COMPASS and where soils are mostly limited by phosphate (57). In the context of the global carbon cycle, the eolian input of nitrogen to marine ecosystems is essentially irrelevant(59). In addition to ecophysiological considerations, land use change plays a major role in the carbon source/sink dynamics. The increased pressure in the developing world to increase food and fiber production by converting forests to agriculturaluse effectively increasesthe flux of carbonto the atmosphere while simultaneouslyreducing the land area available for active sinks. Abandonmentof agricultural land and regrowth of forests, largely in the temperate Northern Hemisphere, may be a significant terrestrialCO2 sink at present (34) but cannot be sustained indefinitely.This sink can buy some time, but unless CO2 emissions are reduced, it cannot mitigate against continued accumulation of the gas in Earth'satmospheregiven projected emission scenarios. The Need for an Integrated Systems Table 2. Examplesof humaninterventionin the globalbiogeochemicalcycles of carbon,nitrogen, Approach sulfur,water,andsediments.Dataarefor the mid-1900s. phosphorus, The global carboncycle is affected by human activities and is coupled to other climatologof flux(millions Magnitude ical and biogeochemical processes. As disof metrictons peryear) %changedue to Element Flux humanactivities cussed above, we have considerableinformation about specific aspects of the carbon cyNatural Anthropogenic cle, but many of the couplings and feedbacks C anddecayCO2 Terrestrial 61,000 respiration are poorly understood. As we drift further +13 Fossilfuel and landuse CO2 8,000 away from the domain that characterizedthe 130 N Naturalbiologicalfixation preindustrialEarth system, we severely test 140 +108 Fixationowingto ricecultivation, the limits of our understandingof how the combustionof fossilfuels,and Earthsystem will respond. of fertilizer production A look at the current understandingof Chemicalweathering 3 P CO2 changes illustrates glacial-interglacial 12 +400 Mining the problem.Perhapssurprisingly,there is no 80 S Naturalemissionsto atmosphereat consensus on the causes of these changes. Earth'ssurface There are at least 11 hypotheses (53, 60, 61), 90 +113 Fossilfuel andbiomassburning which may be grouped into three basic emissions themes: (i) physical/chemical "reorganiza111 x 1012 overland O and H Precipitation tion" of the oceans, (ii) changes in the ocean +16 18 x 1012 (as H20) Globalwaterusage carbonatesystem, and (iii) changes in ocean river 1 x 1010 SedimentsLong-term preindustrial nutrientinventories.Many of these hypothesuspendedload ses are not mutually exclusive. The interac2 x 1010 +200 Modernriversuspendedload tions between marine and terrestrialecosystems, changes in ocean circulation,radiative forcing, and greenhouse gases all probably .400 interactin a specific sequence to give rise to the natural cyclic atmospheric and climatic oscillations. These interactionsare not pres105 ently represented in detailed models of the glacial-interglacialtransitions. 104 This example illustrates three points. First, in the recent history of Earth,the carr' iu bon cycle did not operate in a vacuum and I I I I,DI 103 ......... 50 --150 -400 -300 -250 -200 510 0 -4500 -350 Q. was not constrainedto a specific reservoir. Glacial-interglacial Naturalchanges in the inventoriesof carbon, a 102as inferredfrom the ice core records of glacial-interglacialtransitions,are linked to other biogeochemical and climatological pro< 100 cesses. Those linkages continue to the present, but the quantitativeimpacts in the coming centuryare obscuredby simultaneous 10-1alterations of numerous biogeochemical cycles through human activities. Second, the 10-2 , scientific community has generally ap109 108 107 106 105 104 103 102 101 100 10-1 10-2 10-3 proached problems such as glacial-interglacial transitions from a disciplinary perspecPeriod [years] tive. This approachhas not produced comFig.2. Schematicvariancespectrumfor CO2overthe courseof Earth'shistory.Note the impactof pletely satisfactory explanations for what is humanperturbations on the decade-to-centuryscale. (Inset) Changesin atmosphericCO2overthe natural perturbationin the a past 420,000 years as recordedin the Vostokice, showingthat both the rapidrate of changeand clearly large the increasein CO2concentrationsince the IndustrialRevolutionare unprecedentedin recent global carboncycle. Because of the disciplingeologicalhistory. ary nature of research, interactionsbetween . .. 294 - 13 OCTOBER 2000 VOL290 ., SCIENCEwww.sciencemag.org SCIENCE'S components of the Earth system are not incorporated into present biogeochemical or climate models. When changes in isolated processes are considered, we usually understand the signs of feedbacks, if not the magnitudes of the responses. It is when processes interactthat we have significant problems in reproducing the phenomena quantitatively. Clearly, a systems approachis needed. Third, reconstructionsof the carbon cycle (for example, during glacial-interglacialtransitions) provide testable hypotheses about the Earth system. Consensus on how a 100-ppmv change in atmosphericCO2 can occur naturally within a 100,000-year time frame (62) would imply some understandingof the feedbacks within the Earthsystem. Knowledge of these feedbacks does not give us predictive capability for the coming decades or centuries, but it can help us develop the modeling tools needed to integrate the detailed information gathered from component studies of the contemporaryworld. Our analysis above shows that although naturalsinks can potentially slow the rate of increase in atmosphericCO2, there is no natural savior waiting to assimilate all the anthropogenic CO2 in the coming century. Although on geological time scales the anthropogenic emission of CO2 is a transientphenomenon (Fig. 2), it will affect Earth's biogeochemical cycles for hundredsof years to come (20, 63). Ourpresentimperfectmodels suggest thatthe feedbacksbetween carbon and other biogeochemical and climatological processes will lead to weakened sink strengths in the foreseeable future, and the prospects of retrieving anthropogenic CO2 from the atmosphere by enhancing natural sinks are small. This condition cannot persist indefinitely. Potential remediationstrategies, such as the purposeful manipulationof biological and chemical processes to accelerate the sequestration of atmospheric CO2, are being seriously considered by both governmental bodies and private enterprises.These mitigationstrategieswill themselves have unknown consequences and must be carefully assessed within the context of an integrated systems approachbefore any action is taken. As we rapidly enter a new Earth system domain, the "Anthropocene"Era (64), the debate about distinguishing human effects from naturalvariabilitywill inevitably abate in the face of increased understanding of climate and biogeochemical cycles. Our present state of uncertainty arises largely from lack of integrationof information.Nevertheless, scientists' abilities to predict the future will always have a component of uncertainty.This uncertaintyshould not be confused with lack of knowledge nor should it be used as an excuse to postpone prudentpolicy decisions based on the best informationavailable at the time. COMPASS References and Notes 1. M. I. Hoffert et al., Nature 395, 881 (1998). 2. J. T. Houghton, G. J. Jenkins, J. J. Ephraums,Eds., Climate Change: The IPCC Scientific Assessment (CambridgeUniv. Press, Cambridge,1996). 3. The International Geosphere-Biosphere Programme (IGBP)is an umbrella organization that coordinates (but does not fund) large multinationalresearchprograms. Several of these programs have focused on the carbon cycle in specific reservoirs:The flagship programfor terrestrialecosystems is Global Change and TerrestrialEcosystems (GCTE);for the oceans, it is the Joint GlobalOcean FluxStudy (JGOFS);for the atmosphere, it is InternationalGlobal Atmospheric Chemistry(IGAC);and for paleochemistryand paleoclimate, it is Past Global Changes (PAGES). 4. S. Arrhenius,Philos. Mag. J. Sci. (London,Edinburgh, Dublin) 41, 237 (1896). 5. M. I. Budyko, The Earth'sClimate: Past and Future (Academic Press, New York,1982). 6. J. F. B. Mitchell,T. C.Johns,J. M. Gregory,S. F. B.Tett, Science 376, 501 (1995). 7. H. J. Smith, H. Fischer,M. Wahlen, D. Mastroianni,B. Deck, Nature 400, 248 (1999). 8. J. R. Petit et al., Nature 399, 429 (1999). 9. The reconstruction of paleotemperatures from the ice cores is based on the H/D and 18/160 fractionation in the precipitation. Necessarily, the inferred temperature is that of the upper troposphere, not that at ground level. Moreover,the inferredtemperature is not a global mean but rathera value for the region, in this case, Vostok in Antarctica. Despite these caveats, the glacial-interglacial temperature trends and anomalies are highly consistent on time scales of 100,000 years for the four cycles obtained from the ice core. 10. T. Crowley,Science 289, 270 (2000). 11. On time scales of millions of years, vulcanism and weathering reactions are critical determinants of atmospheric CO2. The weathering reactions can be summarizedby the following: weathering COz+ CaSiO3? CaCO3+ SiOz 12. 13. 14. 15. 16. 17. 18. metamorphosis where Mg can substitute for Ca. CO2 is resuppliedto the atmosphere by vulcanism [J. F. Kasting, O. B. Toon, J. B. Pollack,Sci. Am. 258, 90 (1988)]. On time scales of decades, these processes are relatively insignificant in determining atmospheric CO2 as compared with the exchanges of CO2 between oceanic and terrestrialecosystems. The preindustrialconcentration of CO2 was -280 ppmv throughout the Holocene. The lower mean value is due to the fact that the glacial periods (with low CO2concentrations)were about four times longer than the interglacialperiods. In fact, most of the recent history of Earth is dominated by a glacial climate, with relatively short punctuations of interglacial phases. If the low CO2levels of glacial periods had persisted through the Holocene, plants that provided food and fiber for early human civilizationmay not have been cultivatable [R.F. Sage, Global Change Biology 1, 93 (1995)]. Given projectedrates of increase in atmosphericCO2, the pH of the surface waters will decrease by -0.2 units within this century. This decrease will significantly hinder the biological precipitationof calcium carbonates [J. Klyepas et al., Science 284, 118 (1999); C. Langdonetal., GlobalGeochem. Cycles 14, 639 (2000)]. T. Volk and M. I. Hoffert, in The Carbon Cycle and Atmospheric COz: Natural Variations Archean to Present, E.T. Sunquistand W. S. Broeker,Eds.(American Geophysical Union, Washington, DC, 1985), pp. 99-110. J. L. Sarmiento and M. Bender,Photosynth. Res. 39, 209 (1994). W. S. Broecker and T.-H. Peng, Nature 356, 587 (1992). T. Stocker and A. Schmittner, Nature 388, 862 (1998). S. Manabeand R.J. Stouffer,Nature 364, 215 (1993). www.sciencemag.org SCIENCE VOL290 19. J. L. Sarmiento, T. M. C. Hughes, R. J. Stouffer, S. Manabe,Nature 393, 245 (1998). 20. F. Joos, G.-K. Plattner, T. Stocker, O. Marchal, A. Schmittner,Science 284, 464 (1999). 21. P. G. Falkowski,R. T. Backer,V. Smetacek, Science 281, 200 (1998). 22. E. Laws, P. Falkowski,W. O. Smith, H. Ducklow, J. McCarthy,Global Biogeochem Cycles, in press. 23. This is the apparent steady-state value, not the change in the net exchange with the atmosphere. 24. This so-called "Strangelove"ocean scenario is uncertain within about a factor of 2 because we do not have better estimates of export fluxes of carbon in the oceans (22). 25. This (perhaps counterintuitive)effect is a direct outcome of the calcificationreaction,which can be summarizedas 2HCO3+ Ca <->CaCO3+ COz + H2O.The mean residencetime of Ca in the oceans is 8.5 x 105 years (it is even longer for Mg2+). On time scales of millions of years, as the Ca supply from weathering keeps pace with the precipitationof carbonates,carbonate formationand burialbecome significantsinks for COz.In fact, carbonatesare the largestreservoirof carbonon Earth(Table 1). As COzdissolvesin seawater, it forms carbonicacid, which lowers pH (13). Thus,as atmosphericCOz increases,the pH of the upperocean decreases until the bufferingcapacity of the ocean is restoredby the dissolutionof carbonates. 26. J. L. Sarmiento, T. M. C. Hughes, R. J. Stouffer, S. Manabe,Nature 393, 245 (1998). 27. J. L Sarmiento and U. Siegenthaler,PrimaryProductivity and Biogeochemical Cycles in the Sea, P. G. Falkowski,Ed. (Plenum, New York, 1992), pp. 316317. 28. Followingup on the work of the JGOFSprogram,the responses of marine ecosystems to changes in climate and CO2 in the coming century have been identified by biological oceanographersas a key research topic for the next decade in funding agency planning. 29. The storage of carbon in terrestrial ecosystems is primarilyrelated to the relative resistance of lignin and other polymeric carbon complexes to degradation or herbivory.Terrestrialplants contain, on average, substantially more organic carbon per unit of nitrogen or phosphorus than their marine counterparts, the phytoplankton,which are primarilycomposed of protein. Although lignins and other carbonrich polymers may accumulate in terrestrialecosystems on time scales of decades, on longer time scales most of these molecules are oxidized, so that the accumulationof organic carbon in soils is a miniscule fraction of the total carbon fixed by the ecosystem. Lakesmay also store substantial amounts of organic matter in sediments [W. E. Dean and E. Gorham, Geology 26, 535 (1998)]. 30. R. Myneni,C. Keeling,C. Tucker,G. Asrar,R. Nemani, Nature 386, 698 (1997). 31. P. P, Tans, I. Y. Fung,T. Takahashi,Science 247, 1431 (1990). 32. 33. 34. 35. 36. 37. 38. 39. 40. R.F. Keelingand S. R.Shertz,Nature 358, 723 (1992). M. Battle et al., Science 287, 2467 (2000). S. Fan et al., Science 282, 442 (1998). An invaluablefurtherconstraint on both oceanic and terrestrial carbon uptake is provided by following annual and interannual changes in atmospheric Oz concentrations. With this approach, it is assumed that intraannualdecreases in 0O and increases in CO2 are due to the combined effects of fossil fuel burning and deforestation. Increases in 02 with decreased COz are a consequence of terrestrial uptake, and decreases in CO2with minimal changes in 02 represent oceanic uptake of the former gas. NPPis the difference between gross primaryproduction and plant respiration. D. S. Schimel, Global Change Biol. 1, 77 (1995). S. P. Long and B. G. Drake, Crop Photosynthesis: Spatial and TemporalDeterminants,N. R. Bakerand H. Thomas, Eds. (Elsevier, Amsterdam, 1992), pp. 69-95. C. Kornerand F. Bazzaz,CarbonDioxide, Populations, and Communities(AcademicPress,New York,1996). Because the saturation function of an enzyme is not a linear function of substrate concentration, the relationship between the change in CO2 and rubisco 13 OCTOBER 2000 295 SCIENCE'S 41. 42. 43. 44. 45. 46. 47. 48. 49. 50. 51. activity is not linear. These levels of CO2 can be reached within the next 50 years. M.U. F. Kirschbaum, Soil Biol.Biochem.27, 753 (1995). F. A. Bazzaz,Annu. Rev. Ecol. Syst. 21, 167 (1990). P. Jarvisand S. Linder,Nature 405, 904 (2000). P. Vitousek, H. Mooney, J. Lubchenco,J. Melillo,Science 277, 494 (1997). J. N. Galloway, W. H. Schlesinger, H. Levy, A. Michaels,J. L.Schnoor,GlobalBiogeochem. Cycles 9, 235 (1995). R. Howarth,Ed.,Nitrogen Cyclingin the North Atlantic Ocean and Its Watersheds(KluwerAcademic,Boston, 1996). C. Kroezeand S. Seitzinger,Nutr. Cycl. Agroecosyst. 52, 195 (1998). J. J. Walsh, Nature 350, 53 (1991). J. P. Christensen, J. W. Murray,A. H. Devol, L. A. Codispoti,Global Biogeochem. Cycles 1, 97 (1987). S. P. Seitzingerand A. E. Giblin,Biogeochemistry35, 235 (1996). There are exceptions of course. Phosphoruslimitation occurs in the Mediterraneanand parts of the western 52. 53. 54. 55. 56. 57. 58. 59. 60. 61. COMPASS North Atlantic [J. Wu, W. Sunda, E. Boyle, D. Kari, Science 298, 759 (2000)]. K.Coale et al. Nature 383, 495 (1996). P. Falkowski,Nature 387, 272 (1997). I. Fung et al., Global Biogeochem. Cycles 14, 281 (2000). A. Dai, I. Fung,A. Del Genio,J. Clim. 10, 2943 (1997). The change in nitrogen inventories in the ocean may makes a substantialcontributionto the drawdownof COz on glacial-interglacialtime scales (53, 60). S. Hall and P. Matson, Nature 400, 152 (1999). K.J. Nadelhoffer et al., Nature 398, 145 (1999). The estimated annual global eolian flux of fixed inorganicnitrogen (NOy) to the ocean is 12.3 Tg, of which 9 Tg is from anthropogenic sources (45). Assuming that all that nitrogenwas used to fix CO2,the net stimulation amounts to -65 Tg of carbon per year. This is less than 1% of the global annual anthropogenic emission of CO2. W. S. Broeckerand G. M. Henderson,Paleoceanography 13, 352 (1998). R. Keelingand B. Stephens, Nature 404, 171 (2000). Mind the NEW! Science 62. The transition into glacial periods is gradual, with several phases, and occurs over several tens of thousands of years, whereas the transition to an interglacial state occurs within 10,000 years. 63. J. Sarmiento and C. Le Quere, Science 274, 1346 (1996). 64. P. Crutzen and E. Stoermer, IGBPNewsl. 41, 17 (2000). 65. This article is based on a workshop on the global carbon cycle held at the Royal Swedish Academy of Science in November 1999. The workshopwas organized by the InternationalBiosphere-GeosphereProgramme (IBGP)and the Royal Swedish Academy of Science, in collaboration with Stockholm University and the Swedish Universityof AgriculturalSciences. Financialsupport was provided by the Swedish Millennium Committee and by MISTRA(the Swedish Foundation for Strategic EnvironmentalResearch). The workshopwas the first of five Stockholm workshops contributing to the IGBPsynthesis project. Thanksto J. Raven for comments. gap. 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