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1.
Incorporation of 14C-depleted (old) dissolved organic carbon (DOC) on/into particulate organic carbon (POC) has been suggested as a possible mechanism to explain the low Δ14C-POC values observed in the deep ocean [Druffel, E.R.M., Williams, P.M., 1990. Identification of a deep marine source of particulate organic carbon using bomb 14C. Nature, 347, 172–174.]. A shipboard incubation experiment was performed in the Sargasso Sea to test this hypothesis. Finely ground dried plankton was incubated in seawater samples from the deep Sargasso Sea, both with and without a biological poison (HgCl2). Changes in parameters such as biochemical composition and carbon isotopic signatures of bulk POC and its organic compound classes were examined to study the roles of sorptive processes and biotic activity on POC character. Following a 13-day incubation, the relative abundance of the acid-insoluble organic fraction increased. Abundances of extractable lipids and total hydrolyzable amino acids decreased for both treatments, but by a greater extent in the non-poisoned treatment. The Δ14C values of POC recovered from the non-poisoned treatment were significantly lower than the value of the unaltered plankton material used for the incubation, indicating incorporation of 14C-depleted carbon, most likely DOC. The old carbon was present only in the lipid and acid-insoluble fractions. These results are consistent with previous findings of old carbon dominating the same organic fractions of sinking POC from the deep Northeast Pacific [Hwang, J., Druffel, E.R.M., 2003. Lipid-like material as the source of the uncharacterized organic carbon in the ocean? Science, 299, 881–884.]. However, the Δ14C values of POC recovered from the poisoned treatment did not change as much as those from the non-poisoned treatment suggesting that biological processes were involved in the incorporation of DOC on/into POC.  相似文献   

2.
《Marine Chemistry》2002,79(1):37-47
Profiles of dissolved organic carbon (DOC) were measured in the pore water of sediments from 1000, 2000 and 3500 m water depth in the eastern North Atlantic. A net DOC accumulation in the pore waters was observed, which followed closely the zonation of microbial respiration in these sediments. The concentration of pore water DOC in the zone of oxic respiration was elevated relative to that in the bottom ocean water. The resulting upward gradient across the sediment–water interface indicated a steady state diffusive benthic flux, FDOC, of 0.25–0.44 mmol m−2 day−1 from these sediments. Subsequent increase in the concentration of DOC in the pore water occurred only in the sediments from 1000 and 2000 m water depth that supported anoxic respiration, leading to a deep concentration maximum. By contrast, in the sediments from 3500 m water depth, a deep concentration minimum was measured, coincident with minimal postoxic respiration in this near-abyssal setting. The gradient-based FDOC represented approximately 14% of the total remineralized organic carbon (TCR=sum of FDOC and depth-integrated organic carbon oxidation rate) in the sediments from 1000 and 2000 m water depth, while it was 36% of the TCR in the sediments from 3500 m water depth. A covariance of particulate organic carbon (POC) and pore water DOC with depth in the sediments was evident, more consistently at the deepest site. While the covariance can be related to biotic processes in these sediments, an alternative interpretation suggests a possible contribution of sorption to the biotic control on sedimentary organic carbon cycling. The steady state diagenetic conditions in which this may occur can be conceivable for some organic-poor deep-sea locations, but direct evidence is clearly required to validate them.  相似文献   

3.
基于海洋环流模式POP和生物地球化学模型OCMIP-2,建立了全球海洋碳循环模式,并用于对全球海洋碳循环的模拟研究。该模式在大气CO2为283×10-6条件下,积分3 100 a,达到工业革命前的平衡态。在此基础上,用历史时期观测的大气CO2浓度进行强迫,模拟了历史时期的海洋碳循环。模拟的无机碳浓度、总碱度与基于观测得到的结果基本一致,模式能够较好地模拟全球碳循环过程。模拟结果表明,在北半球中高纬度和南半球的中纬度,海洋是大气CO2的主要汇区;在赤道南北纬20°之间和南大洋50°S以南,海洋表现为大气CO2的源区。在1980s海洋吸收CO2速率(以C计)为1.38 Pg/a,1990s为1.55 Pg/a。海洋中人为碳在北大西洋含量最大,向下到达海底并向南输运到30°N附近;在南极附近,浓度较小,深度达到3 000 m;在中纬度,人为碳被限制在温跃层以上。  相似文献   

4.
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5.
The least known component of the “biological pump” is the active transport of carbon and nutrients by diel vertical migration of zooplankton. We measured CO2 respiration and dissolved organic carbon (DOC) excretion by individual species of common vertically migrating zooplankton at the US JGOFS Bermuda Atlantic Time-series Study (BATS) station. The inclusion of DOC excretion in this study builds on published research on active transport by respiration of inorganic carbon and allows a direct assessment of the role of zooplankton in the production of dissolved organic matter used in midwater microbial processes. On average, excretion of DOC makes up 24% (range=5–42%) of the total C metabolized (excreted+respired) and could represent a significant augmentation to the vertical flux that has already been documented for respiratory CO2 flux by migrant zooplankton. Migratory fluxes were compared to other transport processes at BATS. Estimates of combined active transport of CO2 and DOC by migrators at BATS averaged 7.8% and reached 38.6% of mean sinking POC flux at 150 m, and reached 71.4% of mean sinking POC flux at 300 m. DOC export by migrator excretion averaged 1.9% and reached 13.3% of annual DOC export by physical mixing at this site. During most of the year when deep mixing does not occur, diel migration by zooplankton could provide a supply of DOC to the deeper layers that is available for use by the microbial community. A carbon budget comparing migrant zooplankton transport to the balance of fluxes in the 300–600 m depth strata at BATS shows on average that the total migrant flux supplies 37% of the organic carbon remineralized in this layer, and that migrant DOC flux is more than 3 times the DOC flux gradient by diapycnal mixing. New estimates of active transport of both organic and inorganic carbon by migrants may help resolve observed imbalances in the C budget at BATS, but the magnitude is highly dependent on the biomass of the migrating community.  相似文献   

6.
The likelihood that the carbon fluxes measured as part of the US-JGOFS field program in the equatorial Pacific ocean (EgPac) during 1992 yielded a balanced carbon budget for the surface ocean was determined. The major carbon fluxes incorporated into a surface carbon budget were: new production, particulate organic carbon (POC) and dissolved organic carbon (DOC) export, CaC03 export, C02 gas evasion, dissolved inorganic carbon (DIC) supply, and the time rate of charge. The ratio of the measured concentration gradients of DOC and DIC provided a constraint on the ratio of POC/DOC export. Uncertainties of ±30–50% for individual carbon flux measurements reduce the likelihood that a carbon balance can be measured during a JGOFS process-type study. As a benchmark, carbon fluxes were prescribed to yield a hypothetical surface carbon budget that was, on average, balanced. Given the typical errors in the individual carbon fluxes, however, there was only about a 30% chance that this hypothetical budget could be measured to be balanced to ±50%. Using this benchmark, it was determined that there was a 95 % chance that the carbon flux measurements yielded a surface DIC budget balanced (to ±50%) during El Nino conditions in boreal spring 1992, when the total organic carbon export rate was - 5 mmol C m-2 day- 1 and the POC export was 3 mmol C m−2 day−1. In boreal fall 1992, during cold period conditions, there was a 70% chance that the surface carbon DIC budget was balanced when the total organic carbon export rate was 20 mmol C m−2 day−1 and export was -13 mmol C m-2 day-'. The DOC to DIC concentration gradient ratio of - -0.15, measured in depth profiles down to 100m and in surface waters, was used as an important constraint that most (> 70%) of the organic carbon exported from the euphotic zone was POC rather than DOC. If a balanced surface DIC budget was used to test the compatibility of individual carbon fluxes measured during EgPac, then a three- to four-fold increase in total and particulate organic carbon export between spring and fall is indicated. This increase was not reflected in the POC loss rates measured by drifting sediment trap collections or estimated by234Th deficiencies coupled with the C/Th measured on suspended particles.  相似文献   

7.
Iron fertilization of nutrient-rich surface waters of the ocean is one possible way to help slow the rising levels of atmospheric CO2 by sequestering it in the oceans via biological carbon export. Here, I use an ocean general circulation model to simulate a patch of nutrient depletion in the subpolar northwest Pacific under various scenarios. Model results confirm that surface fertilization is an inefficient way to sequester carbon from the atmosphere (Gnanadesikan et al., 2003), since only about 20% of the exported carbon comes initially from the atmosphere. Fertilization reduces future production and thus CO2 uptake by utilizing nutrients that would otherwise be available later. Effectively, this can be considered as leakage when compared to a control run. This “effective” leakage and the actual leakage of sequestered CO2 cause a significant, rapid decrease in carbon retention (only 30–45% retained after 10 years and less than 20% after 50 years). This contrasts markedly with the almost 100% retention efficiency for the same duration using the same model, when carbon is disposed directly into the northwest Pacific (Matsumoto and Mignone, 2005). As a consequence, the economic effectiveness of patch fertilization is poor in two limiting cases of the future price path of carbon. Sequestered carbon in patch fertilization is lost to the atmosphere at increasingly remote places as time passes, which would make monitoring exceedingly difficult. If all organic carbon from one-time fertilization reached the ocean bottom and remineralized there, acidification would be about −0.05 pH unit with O2 depletion about −20 μmol kg−1. These anomalies are probably too small to seriously threaten deep sea biota, but they are underestimated in the model because of its large grid size. The results from this study offer little to advocate purposeful surface fertilization as a serious means to address the anthropogenic carbon problem.  相似文献   

8.
This article presents the results of long-term studies of the dynamics of carbonate parameters and air–sea carbon dioxide fluxes on the Chukchi Sea shelf during the summer. As a result of the interaction of physical and biological factors, the surface waters on the west of Chukchi Sea were undersaturated with carbon dioxide when compared with atmospheric air; the partial pressure of CO2 varied in the range from 134 to 359 μatm. The average value of CO2 flux in the Chukchi Sea per unit area varied in the range from–2.4 to–22.0 mmol /(m2 day), which is significantly higher than the average value of CO2 flux in the World Ocean. It has been estimated that the minimal mass of C absorbed by the surface of Chukchi Sea from the atmosphere during ice-free season is 13 × 1012 g; a great part of this carbon is transported to the deeper layers of sea and isolated from the atmosphere for a long period of time. The studies of the carbonate system of the Chukchi Sea, especially of its western part, will provide some new data on the fluxes of carbon dioxide in the Arctic Ocean and their changes. Our analysis can be used for an interpretation of the satellite assessment of CO2 fluxes and dissolved CO2 distribution in the upper layers of the ocean.  相似文献   

9.
Effects of CO<Subscript>2</Subscript> Enrichment on Marine Phytoplankton   总被引：1，自引：0，他引：1  
Rising atmospheric CO2 and deliberate CO2 sequestration in the ocean change seawater carbonate chemistry in a similar way, lowering seawater pH, carbonate ion concentration and carbonate saturation state and increasing dissolved CO2 concentration. These changes affect marine plankton in various ways. On the organismal level, a moderate increase in CO2 facilitates photosynthetic carbon fixation of some phytoplankton groups. It also enhances the release of dissolved carbohydrates, most notably during the decline of nutrient-limited phytoplankton blooms. A decrease in the carbonate saturation state represses biogenic calcification of the predominant marine calcifying organisms, foraminifera and coccolithophorids. On the ecosystem level these responses influence phytoplankton species composition and succession, favouring algal species which predominantly rely on CO2 utilization. Increased phytoplankton exudation promotes particle aggregation and marine snow formation, enhancing the vertical flux of biogenic material. A decrease in calcification may affect the competitive advantage of calcifying organisms, with possible impacts on their distribution and abundance. On the biogeochemical level, biological responses to CO2 enrichment and the related changes in carbonate chemistry can strongly alter the cycling of carbon and other bio-active elements in the ocean. Both decreasing calcification and enhanced carbon overproduction due to release of extracellular carbohydrates have the potential to increase the CO2 storage capacity of the ocean. Although the significance of such biological responses to CO2 enrichment becomes increasingly evident, our ability to make reliable predictions of their future developments and to quantify their potential ecological and biogeochemical impacts is still in its infancy. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

10.
We report here the non-conservative behaviour of DOC in the northwestern Indian Ocean by studying this parameter together with other carbon and nitrogen components. This contrasts with earlier reports of conservative behaviour. Concentrations of DOC, 3–4 times higher than those reported earlier, were found to decrease northward from the equator. Total carbon dioxide (TCO2) increases in proportion of the oxygen utilized, thus revealing the dominant biological role in the carbon turnover. The CO2 added through dissolution of biogenic debris is found to decrease southward, in general. Decomposition of organic material contributes at least 64% to the CO2 addition that increases southward, the rest being from dissolution of skeletal material. Evidence is provided for the utilization of oxygen and nitrate for DOC oxidative decomposition. Accumulation of DOC without its complete oxidation to CO2 could be the main reason for the TCO2 decrease in southern Arabian Sea. Relationships of DOC with nitrification and denitrification processes show that the microbial population plays a major role in regulating the DOC contents in the seawater of this region. Consumption/decomposition by denitrifying bacteria and other micro-organisms responsible for nitrogen cycling in the sea are found to be intimately related to the DOC dynamics and are responsible for decreased DOC concentrations in the north. DOC accumulation in the southern Arabian Sea seems to facilitate bacterio-particulate aggregate formation and consequent nitrification, which results in excess nitrate. Application of a one-dimensional advection-diffusion model to the present data set provides evidence for the non-conservative nature of DOC in the Arabian Sea.  相似文献   

11.
The distribution and optical absorption characteristics of chromophoric dissolved organic matter (CDOM) were systematically investigated along three meridional transects in the North Atlantic Ocean and Caribbean Sea conducted as part of the 2003 US CLIVAR/CO2 Repeat Hydrography survey. Hydrographic transects covered in aggregate a latitudinal range of 5° to 62° north along longitudes 20°W (line A16N, Leg 1), 52°W (A20), and 66°W (A22). Absorption spectra of filtered seawater samples were collected and analyzed for depths ranging from the surface to ∼6000 m, sampling all the ocean water masses in the western basin of the subtropical North Atlantic and several stations on the North and South American continental slopes. The lowest surface abundances of CDOM (< 0.1 m−1 absorption coefficient at 325 nm) were found in the central subtropical gyres while the highest surface abundances (∼0.7 m−1) were found along the continental shelves and within the subpolar gyre, confirming recent satellite-based assessments of surface CDOM distribution. Within the ocean interior, CDOM abundances were relatively high (0.1–0.2 m−1 absorption coefficient at 325 nm) except in the subtropical mode water, where a local minimum exists due to the subduction of low CDOM surface waters during mode water formation. In the subthermocline water masses of the western basin, changes in CDOM abundance are not correlated with increasing ventilation age as assessed using chlorofluorocarbon (CFC) concentrations and the atmospheric CFC history. But dissolved organic carbon (DOC) mass-specific absorption coefficients of CDOM increase with increasing ventilation age in the deep sea, indicating that CDOM is a refractory component of the DOC pool. The overall CDOM distribution in the North Atlantic reflects the rapid advection and mixing processes of the basin and demonstrates that remineralization in the ocean interior is not a significant sink for CDOM. This supports the potential of CDOM as a tracer of ocean circulation processes for subducted water masses.  相似文献   

12.
Along with meteorological observations, complementary and systematic oceanographic observations of various physical, biological and chemical parameters have been made at Ocean Station P (OSP) (50°N, 145°W) since the early 1950s. These decadal time scale data have contributed to a better understanding of the physical, biological and chemical processes in the surface layer of the northeastern subarctic region of the Pacific Ocean. These data have demonstrated the importance of the North Pacific in the global carbon cycle and, in particular, the role of biological/chemical processes in the net exchange of CO2 across the air–sea interface. Although we do not fully comprehend how climatic variations influence marine communities or marine biogeochemistry, previous studies have provided some basic understanding of the mechanisms controlling the seasonal and inter-annual variations of biological and chemical parameters (such as phytoplankton, bacteria, nitrate/ammonium concentration) at OSP, and how they affect the carbon cycling in the subarctic North Pacific. In this study, we investigate how these mechanisms might alter the seasonal variations of these parameters at OSP under a 2XCO2 condition. We examine these influences using a new biological model calibrated by the climatological data from OSP. For the 2XCO2 simulation, the biological model is driven off line (i.e., no feedback to the ocean/atmospheric model components) by the climatology plus 2XCO2−1XCO2 outputs from a global surface ocean model and the Canadian GCM. Under the 2XCO2 condition, the upper layer ocean shows an increase in the entrainment rate at the bottom of the mixed layer for OSP during the late autumn and winter seasons, resulting in an increase in the f-ratio. Although there is an overall increase in the primary production (PP) by 3–18%, a decrease in the biomass of small phytoplankton and microzooplankton (due to mesozooplankton grazing) lowers the concentration of dissolved organic matter (DOM) by 4–25%. The model also predicts a significant increase in the concentrations of nitrate and ammonium, and in bacterial production during July and August. Doubling of the atmospheric CO2 from 330 to 660 ppm forces the marine pCO2 to increase by about 63%, much of which is driven by an increased flux of CO2 from the atmosphere to the oceans.  相似文献   

13.
A preliminary study of carbon system in the East China Sea   总被引：1，自引：0，他引：1  
In the central part of the East China Sea, the activity of CO2 in the surface water and total carbonate, pH and alkalinity in the water column were determined in winter and autumn of 1993. The activity of CO2 in the continental shelf water was about 50 ppm lower than that of surface air. This decrease corresponds to the absorption of about 40 gC/m2/yr of atmospheric CO2 in the coastal zone or 1 GtC/yr in the global continental shelf, if this rate is applicable to entire coastal seas. The normalized total carbonate contents were higher in the water near the coast and near the bottom. This increase toward the bottom may be due to the organic matter deposited on the bottom. This conclusion is supported by the distribution of pH. The normalized alkalinity distribution also showed higher values in the near-coast water, but in the surface water, indicating the supply of bicarbonate from river water. The residence time of the East China Sea water, including the Yellow Sea water, has been calculated to be about 0.8 yr from the excess alkalinity and the alkalinity input. Using this residence time and the excess carbonate, we can estimate that the amount of dissolved carbonate transported from the coastal zone to the oceanic basin is about 70 gC/m2/yr or 2 GtC/yr/area-of-global-continental-shelf. This also means that the rivers transport carbon to the oceans at a rate of 30 gC/m2/yr of the coastal sea or 0.8 GtC/yr/ area-of-global shelf, the carbon consisting of dissolved inorganic carbonate and terrestrial organic carbon decomposed on the continental shelf.  相似文献   

14.
During the 1993–1995 period of minimal deep convection in the Greenland Sea, the dissolved inorganic carbon concentration within the surface waters varied dramatically on the seasonal time scale, with average summer and winter values of 2064 (±10) and 2150 (±5) μmol kg−1, respectively, indicative of a vigorous annual carbon cycle. In contrast, there was very little interannual variability throughout these three years. While primary production largely depleted the surface nutrient supplies in spring and summer, generating a strong seasonal CO2 drawdown, a combination of relatively shallow remineralization and mixed-layer deepening brought essentially all of the carbon consumed by photosynthesis back into contact with the atmosphere before winter. This re-release of the inorganic carbon that had been consumed by phytoplankton earlier in the year was more than sufficient to counteract the cooling-induced increase in the carbon carrying capacity of the water during fall and winter, reducing the potential for atmospheric carbon dioxide absorption by the Greenland Sea over the same period.  相似文献   

15.
Results from numerical experiments with an atmosphere-ocean general circulation model coupled to the carbon evolution cycle are analyzed. The model is used to carry out an experiment on the simulation of the climate and carbon cycle change in 1861–2100 under a specified scenario of the carbon dioxide emission from fossil fuel and land use. The spatial distribution of vegetation, soil, and oceanic carbon in the 20th century is generally close to available estimates from observational data. The model adequately reproduces the observed growth of atmospheric CO2 in the 20th century and the uptake of excess carbon by land ecosystems and by the ocean in the 1980s and 1990s. By 2100, the atmospheric CO2 concentration is calculated to reach 742 ppmv under emission and land-use scenario A1B. The feedback between climate change and the carbon cycle in the model is positive, with a coefficient close to the mean of all the current models. The ocean and land uptakes of the CO2 emission by 2100 in the model are 25 and 19%, which are also close to the mean over all models.  相似文献   

16.
This modeling study investigates the impacts of increasing atmospheric CO2 concentration on acidification in the East Sea. A historical simulation for the past three decades (1980 to 2010) was performed using the Hadley Centre Global Environmental Model (version 2), a coupled climate model with atmospheric, terrestrial and ocean cycles. As the atmospheric CO2 concentration increased, acidification progressed in the surface waters of the marginal sea. The acidification was similar in magnitude to observations and models of acidification in the global ocean. However, in the global ocean, the acidification appears to be due to increased in-situ oceanic CO2 uptake, whereas local processes had stronger effects in the East Sea. pH was lowered by surface warming and by the influx of water with higher dissolved inorganic carbon (DIC) from the northwestern Pacific. Due to the enhanced advection of DIC, the partial pressure of CO2 increased faster than in the overlying air; consequently, the in-situ oceanic uptake of CO2 decreased.  相似文献   

17.
Intense studies of upper and deep ocean processes were carried out in the Northwestern Indian Ocean (Arabian Sea) within the framework of JGOFS and related projects in order to improve our understanding of the marine carbon cycle and the ocean’s role as a reservoir for atmospheric CO2. The results show a pronounced monsoon-driven seasonality with enhanced organic carbon fluxes into the deep-sea during the SW Monsoon and during the early and late NE Monsoon north of 10°N. The productivity is mainly regulated by inputs of nutrients from subsurface waters into the euphotic zone via upwelling and mixed layer-deepening. Deep mixing introduces light limitation by carrying photoautotrophic organisms below the euphotic zone during the peak of the NE Monsoon. Nevertheless, deep mixing and strong upwelling during the SW Monsoon provide an ecological advantage for diatoms over other photoautotrophic organisms by increasing the silica concentrations in the euphotic zone. When silica concentrations fall below 2 μmol l−1, diatoms lose their dominance in the plankton community. During diatom-dominated blooms, the biological pathway of uptake of CO2 (the biological pump) appears to be more efficient than during blooms of other organisms, as indicated by organic carbon to carbonate carbon (rain) ratios. Due to the seasonal alternation of diatom and non-diatom dominated exports, spatial variations of the annual mean rain ratios are hardly discernible along the main JGOFS transect.Data-based estimates of the annual mean impact of the biological pump on the fCO2 in the surface water suggest that the biological pump reduces the increase of fCO2 in the surface water caused by intrusion of CO2-enriched subsurface water by 50–70%. The remaining 30 to 50% are attributed to CO2 emissions into the atmosphere. Rain ratios up to 60% higher in river-influenced areas off Pakistan and in the Bay of Bengal than in the open Arabian Sea imply that riverine silica inputs can further enhance the impact of the biological pump on the fCO2 in the surface water by supporting diatom blooms. Consequently, it is assumed that reduced river discharges caused by the damming of major rivers increase CO2 emission by lowering silica inputs to the Arabian Sea; this mechanism probably operates in other regions of the world ocean also.  相似文献   

18.
A procedure is described for the analysis of the stable carbon isotopic composition of dissolved organic carbon (DOC) in natural waters from marine and higher-salinity environments. Rapid (less than 5 min) and complete oxidation of DOC is achieved using a modification of previous photochemical oxidation techniques. The CO2 evolved from DOC oxidation can be collected in less than 10 min for isotopic analysis. The procedure is at present suitable for oxidation and collection of 1–5 μmol of carbon and has an associated blank of 0.1–0.2 μmol of carbon.Complete photochemical oxidation of DOC standards was demonstrated by quantitative recovery of CO2 as measured manometrically. Isotopic analyses of standards by photochemical and high-temperature sealed-tube combustion methods agreed to within 0.3.. Photochemical oxidation of DOC in a representative sediment pore-water sample was also quantitative, as shown by the excellent agreement between the photochemical and sealed-tube methods. The δ13C values obtained for pore-water DOC using the two methods of oxidation were identical, suggesting that the modified photochemical method is adequate for the isotopically non-fractionated oxidation of pore-water DOC.The procedure was evaluated through an analysis of DOC in pond and pore waters from a hypersaline microbial mat environment. Concentrations of DOC in the water column over the mat displayed a diel pattern, but the isotopic composition of this DOC remained relatively constant (average δ13C = −12.4.). Pore-water DOC exhibited a distinct concentration maximum in the mat surface layer, and δ13C of pore-water DOC was nearly 8. lighter at 1.5–2.0-cm depth than in the mat surface layer (0–0.5-cm depth). These results demonstrate the effectiveness of the method in elucidating differences in DOC concentration and δ13C over biogeochemically relevant spatial and temporal scales. Carbon isotopic analysis of DOC in natural waters, especially pore waters, should be a useful probe of biogeochemical processes in recent environments.  相似文献   

19.
Detection and attribution of hydrographic and biogeochemical changes in the deep ocean are challenging due to the small magnitude of their signals and to limitations in the accuracy of available data. However, there are indications that anthropogenic and climate change signals are starting to manifest at depth. The deep ocean below 2000 m comprises about 50% of the total ocean volume, and changes in the deep ocean should be followed over time to accurately assess the partitioning of anthropogenic carbon dioxide (CO2) between the ocean, terrestrial biosphere, and atmosphere. Here we determine the changes in the interior deep-water inorganic carbon content by a novel means that uses the partial pressure of CO2 measured at 20 °C, pCO2(20), along three meridional transects in the Atlantic and Pacific oceans. These changes are measured on decadal time scales using observations from the World Ocean Circulation Experiment (WOCE)/World Hydrographic Program (WHP) of the 1980s and 1990s and the CLIVAR/CO2 Repeat Hydrography Program of the past decade. The pCO2(20) values show a consistent increase in deep water over the time period. Changes in total dissolved inorganic carbon (DIC) content in the deep interior are not significant or consistent, as most of the signal is below the level of analytical uncertainty. Using an approximate relationship between pCO2(20) and DIC change, we infer DIC changes that are at the margin of detectability. However, when integrated on the basin scale, the increases range from 8–40% of the total specific water column changes over the past several decades. Patterns in chlorofluorocarbons (CFCs), along with output from an ocean model, suggest that the changes in pCO2(20) and DIC are of anthropogenic origin.  相似文献   

20.
The multiple-parameter linear regression method (Monitoring global ocean carbon inventories. Ocean Observing System Development Panel, Texas A&M University, College Station, TX, 1995, 54pp; Global Biogeochem. Cycles 13 (1999) 179) is used to compare inorganic carbon data from the GEOSECS CO2 survey in the Pacific Ocean in 1973 to the WOCE/JGOFS global CO2 survey in the 1990s. A model of total dissolved inorganic carbon (DIC) as a function of five variables (AOU, θ, S, Si, and PO4) has been developed from the recent CO2 survey data (namely CGC91 and CGC96) in the Pacific Ocean. After correcting for a systematic DIC offset of −30.3±7 μmol kg−1 from the GEOSECS data, the residual DIC based on this model as computed from GEOSECS data has been used to estimate the anthropogenic CO2 penetration in the Pacific Ocean. In the Northeast Pacific, we obtained an increase of CO2 of 21.3±7.9 mol m−2 over the period from GEOSECS in 1973 to CGC91 in 1991. This gives a mean anthropogenic CO2 uptake rate of 1.3±0.5 mol m−2 yr−1 over this 17 year time period. In the South Pacific, north of 50°S between 180° and 120°W region, the integrated anthropogenic CO2 inventory is estimated to be 19.7±5.7 mol m−2 over the period from GEOSECS in 1974 to CGC96 in 1996. The equivalent mean CO2 uptake rate is estimated to be 0.9±0.3 mol m−2 yr−1 over the 22 years. These results are compared with the isopycnal method (Nature 396 (1998) 560) to estimate the anthropogenic CO2 signal in the Northeast Pacific (30°N, 152°W) at the crossover region between CGC91 and GEOSECS. The results of the isopycnal method are consistent with those derived from the MLR method. Both methods show an increase in anthropogenic CO2 inventory in the ocean over two decades that is consistent with the increase expected if the ocean uptake has kept pace with the atmospheric CO2 increase.  相似文献   

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