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1.
The absorption of anthropogenic CO2 and atmospheric deposition of acidity can both contribute to the acidification of the global ocean. Rainfall pH measurements and chemical compositions monitored on the island of Bermuda since 1980, and a long-term seawater CO2 time-series (1983–2005) in the subtropical North Atlantic Ocean near Bermuda were used to evaluate the influence of acidic deposition on the acidification of oligotrophic waters of the North Atlantic Ocean and coastal waters of the coral reef ecosystem of Bermuda. Since the early 1980's, the average annual wet deposition of acidity at Bermuda was 15 ± 14 mmol m− 2 year− 1, while surface seawater pH decreased by 0.0017 ± 0.0001 pH units each year. The gradual acidification of subtropical gyre waters was primarily due to uptake of anthropogenic CO2. We estimate that direct atmospheric acid deposition contributed 2% to the acidification of surface waters in the subtropical North Atlantic Ocean, although this value likely represents an upper limit. Acidifying deposition had negligible influence on seawater CO2 chemistry of the Bermuda coral reef, with no evident impact on hard coral calcification.  相似文献   

2.
Strong seasonal patterns in upper ocean total carbon dioxide (TCO2), alkalinity (TA) and calculated pCO2 were observed in a time series of water column measurements collected at the US Joint Global Ocean Flux Study (JGOFS) BATS site (31 °50′N, 64 °10′W) in the Sargasso Sea. TA distribution was a conservative function of salinity. However, in February 1992, a non-conservative decrease in TA was observed, with maximum depletion of 25–30 μmoles kg−1 occuring in the surface layer and at the depth of the chlorophyll maximum (˜ 80–100 m). Mixed-layer TCO2 also decreased, while surface pCO2 increased by 25–30 μatm. We suggest these changes in carbon dioxide species resulted from open-ocean calcification by carbonate-secreting organisms rather than physical processes. Coccolithophore calcification is the most likely cause of this event although calcification by foraminifera or pteropods cannot be ruled out. Due to the transient increase in surface pCO2, the net annual transfer of CO2 into the ocean at BATS was reduced. These observations demonstrate the potential importance of open-ocean calcification and biological community structure in the biogeochemical cycling of carbon.  相似文献   

3.
The ‘International Intercomparison Exercise of fCO2 Systems’ was carried out in 1996 during the R/V Meteor Cruise 36/1 from Bermuda/UK to Gran Canaria/Spain. Nine groups from six countries (Australia, Denmark, France, Germany, Japan, USA) participated in this exercise, bringing together 15 participants with seven underway fugacity of carbon dioxide (fCO2) systems, one discrete fCO2 system, and two underway pH systems, as well as systems for discrete measurement of total alkalinity and total dissolved inorganic carbon. Here, we compare surface seawater fCO2 measured synchronously by all participating instruments. A common infrastructure (seawater and calibration gas supply), different quality checks (performance of calibration procedures for CO2, temperature measurements) and a common procedure for calculation of final fCO2 were provided to reduce the largest possible amount of controllable sources of error. The results show that under such conditions underway measurements of the fCO2 in surface seawater and overlying air can be made to a high degree of agreement (±1 μatm) with a variety of possible equilibrator and system designs. Also, discrete fCO2 measurements can be made in good agreement (±3 μatm) with underway fCO2 data sets. However, even well-designed systems, which are operated without any obvious sign of malfunction, can show significant differences of the order of 10 μatm. Based on our results, no “best choice” for the type of the equilibrator nor specifics on its dimensions and flow rates of seawater and air can be made in regard to the achievable accuracy of the fCO2 system. Measurements of equilibrator temperature do not seem to be made with the required accuracy resulting in significant errors in fCO2 results. Calculation of fCO2 from high-quality total dissolved inorganic carbon (CT) and total alkalinity (AT) measurements does not yield results comparable in accuracy and precision to fCO2 measurements.  相似文献   

4.
The interannual variations of CO2 sources and sinks in the surface waters of the Antarctic Ocean (south of 50°S) were studied between 1986 and 1994. An existing, slightly modified one-dimensional model describing the mixed-layer carbon cycle was used for this study and forced by available satellite-derived and climatological data. Between 1986 and 1994, the mean Antarctic Ocean CO2 uptake was 0.53 Pg C year−1 with an interannual variability of 0.15 Pg C year−1.Interannual variation of the Antarctic Ocean CO2 uptake is related to the Antarctic Circumpolar Wave (ACW), which affects sea surface temperature (SST), wind-speed and sea-ice extent. The CO2 uptake in the Antarctic Ocean has increased from 1986 to 1994 by 0.32 Pg C. It was found that over the 9 years, the surface ocean carbon dioxide fugacity (fCO2) increase was half that of the atmospheric CO2 increase inducing an increase of the air–sea fCO2 gradient. This effect is responsible for 60% of the Antarctic Ocean CO2 uptake increase between 1986 and 1994, as the ACW effect cancels out over the 9 years investigated.  相似文献   

5.
In order to construct monthly fields of sea surface fugacity of carbon dioxide (fCO2) on a large scale in the Indian Ocean, we use a one-dimensional model which takes into account the main physical and biogeochemical processes controlling fCO2 variations in the ocean. Physical and biogeochemical processes are constrained by the monthly variations of sea surface temperature, salinity, chlorophyll concentration, wind speed and mixed-layer depth. The model is applied to four locations in the Indian Ocean and it well predicts observed temporal variations in fCO2 at these locations. Regarding to monthly fCO2 observations, the model also well simulates the fCO2 distribution and its temporal variations along a track located between 20 ° and 50 °S with a maximal error of + 10 μatm. The model is also used to predict fCO2 for 2 ° × 2 ° grids over the entire Indian Ocean and simulates seasonal cycles that are consistent with observations. The monthly fCO2 fields derived from the model are used to estimate a global air-sea CO2 flux over the Indian Ocean basin. We estimate a net sink of 0.5 Gt/yr C for the Indian Ocean (20 °N-50 °S), with the main sink located between 20 ° and 50 °S.  相似文献   

6.
Carbon dioxide flux techniques performed during GasEx-98   总被引：2，自引：0，他引：2  
A comprehensive study of air–sea interactions focused on improving the quantification of CO2 fluxes and gas transfer velocities was performed within a large open ocean CO2 sink region in the North Atlantic. This study, GasEx-98, included shipboard measurements of direct covariance CO2 fluxes, atmospheric CO2 profiles, atmospheric DMS profiles, water column mass balances of CO2, and measurements of deliberate SF6–3He tracers, along with air–sea momentum, heat, and water vapor fluxes. The large air–sea differences in partial pressure of CO2 caused by a springtime algal bloom provided high signals for accurate CO2 flux measurements. Measurements were performed over a wind speed range of 1–16 m s−1 during the three-week process study. This first comparison between the novel air-side and more conventional water column measurements of air–sea gas transfer show a general agreement between independent air–sea gas flux techniques. These new advances in open ocean air–sea gas flux measurements demonstrate the progress in the ability to quantify air–sea CO2 fluxes on short time scales. This capability will help improve the understanding of processes controlling the air–sea fluxes, which in turn will improve our ability to make regional and global CO2 flux estimates.  相似文献   

7.
Dissolved oxygen (DO) in the ocean is a tracer for most ocean biogeochemical processes including net community production and remineralization of organic matter which in turn constrains the biological carbon pump. Knowledge of oxygen dynamics in the North Atlantic Ocean is mainly derived from observations at the Bermuda Atlantic Time-series Study (BATS) site located in the western subtropical gyre which may skew our view of the biogeochemistry of the subtropical North Atlantic. This study presents and compares a 15 yr record of DO observations from ESTOC (European Station for Time-Series in the Ocean, Canary Islands) in the eastern subtropical North Atlantic with the 20 yr record at BATS. Our estimate for net community production of oxygen was 2.3±0.4 mol O2 m−2 yr−1 and of oxygen consumption was −2.3±0.5 mol O2 m−2 yr−1 at ESTOC, and 4 mol O2 m−2 yr−1 and −4.4±1 mol m−2 yr−1 at BATS, respectively. These values were determined by analyzing the time-series using the Discrete Wavelet Transform (DWT) method. These flux values agree with similar estimates from in-situ observational studies but are higher than those from modeling studies. The difference in net oxygen production rates supports previous observations of a lower carbon export in the eastern compared to the western subtropical Atlantic. The inter-annual analysis showed clear annual cycles at BATS whereas longer cycles of nearly 4 years were apparent at ESTOC. The DWT analysis showed trends in DO anomalies dominated by long-term perturbations at a basin scale for the consumption zones at both sites, whereas yearly cycles dominated the production zone at BATS. The long-term perturbations found are likely associated with ventilation of the main thermocline, affecting the consumption and production zones at ESTOC.  相似文献   

8.
Diurnal changes in seawater temperature affect the amount of air–sea gas exchange taking place through changes in solubility and buoyancy-driven nocturnal convection, which enhances the gas transfer velocity. We use a combination of in situ and satellite derived radiometric measurements and a modified version of the General Ocean Turbulence Model (GOTM), which includes the National Oceanic and Atmospheric Administration Coupled-Ocean Atmospheric Response Experiment (NOAA-COARE) air–sea gas transfer parameterization, to investigate heat and carbon dioxide exchange over the diurnal cycle in the Tropical Atlantic. A new term based on a water-side convective velocity scale (w*w) is included, to improve parameterization of convectively driven gas transfer. Meteorological data from the PIRATA mooring located at 10°S10°W in the Tropical Atlantic are used, in conjunction with cloud cover estimates from Meteosat-7, to calculate fluxes of longwave, latent and sensible heat along with a heat budget and temperature profiles during February 2002. Twin model experiments, representing idealistic and realistic conditions, reveal that over daily time scales the additional contribution to gas exchange from convective overturning is important. Increases in transfer velocity of up to 20% are observed during times of strong insolation and low wind speeds (<6 m s−1); the greatest enhancement from w*w to the CO2 flux occurs when diurnal warming is large. Hence, air–sea fluxes of CO2 calculated using simple parameterizations underestimate the contribution from convective processes. The results support the need for parameterizations of gas transfer that are based on more than wind speed alone and include information about the heat budget.  相似文献   

9.
Changes in patterns of undetectability and molar ratios of dissolved nutrients in the euphotic zone of the oligotrophic western North Atlantic Ocean were investigated utilizing the Bermuda Atlantic Time-series Study (BATS) data set of the US Joint Global Ocean Flux Study (JGOFS). Our aim was to examine the temporal dynamics of nutrient stocks over a decade (1989∼1998) and to gain insight into the interactions between the different biotic and abiotic factors underlying BATS. Patterns of nutrient undetectability clearly revealed the depleted nature of the nutrients in surface water at the BATS location, particularly phosphorous. The N:P ratio was consistently far above the nominal Redfield ratio (mean, 38.5) but was significantly lower during the 1993∼1994 period (22.1). Over the same period the proportion of samples depleted in N only increased while the proportion of samples depleted in P only decreased. This indicates an overall reduction of N relative to P in the surface water at BATS during the 1993∼1994 period, the reasons for this anomaly, though, are not clear. The correlation analysis between the biotic and abiotic variables at BATS has indicated some interesting relationships that can help understand some of the parameters affecting nutrient stocks in the euphotic zone and their consequent impacts on marine biota. Although nutrient stocks in the oligotrophic environment are limited, they might be subject to interannual variation that may become anomalous in some cases. These variations might underlay significant feedback mechanisms by affecting marine productivity, the prime factor controlling the sequestration of atmospheric CO2 by the oceans. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

10.
This paper evaluates whether a thermodynamic ocean-carbon model can be used to predict the monthly mean global fields of the surface-water partial pressure of CO2 (pCO2SEA) from sea surface salinity (SSS), temperature (SST), and/or nitrate (NO3) concentration using previously published regional total inorganic carbon (CT) and total alkalinity (AT) algorithms. The obtained pCO2SEA values and their amplitudes of seasonal variability are in good agreement with multi-year observations undertaken at the sites of the Bermuda Atlantic Timeseries Study (BATS) (31°50’N, 60°10’W) and the Hawaiian Ocean Time-series (HOT) (22°45’N, 158°00’W). By contrast, the empirical models predicted CT less accurately at the Kyodo western North Pacific Ocean Time-series (KNOT) site (44°N, 155°E) than at the BATS and HOT sites, resulting in greater uncertainties in pCO2SEA predictions. Our analysis indicates that the previously published empirical CT and AT models provide reasonable predictions of seasonal variations in surface-water pCO2SEA within the (sub) tropical oceans based on changes in SSS and SST; however, in high-latitude oceans where ocean biology affects CT to a significant degree, improved CT algorithms are required to capture the full biological effect on CT with greater accuracy and in turn improve the accuracy of predictions of pCO2SEA.  相似文献   

11.
We compared in-situ and satellite-derived measures of the biological carbon pump efficiency at the two seemingly similar subtropical North Atlantic gyre time series sites, the Bermuda time series (BATS, Bermuda Atlantic time-series study and OFP, ocean flux program) in the western gyre and the ESTOC time series (European station for time-series in the ocean, Canary Islands) in the eastern gyre. Satellite-derived surface chlorophyll a was slightly lower at Bermuda compared to ESTOC (annual average of 0.10±0.04 vs. 0.14±0.05-mg-m?3), as was satellite-derived primary production (annual average of 380±77 vs. 440±80-mg C-m?2 d?1). However, export production normalized to primary production (export ratio) was higher at Bermuda by a factor of 2–3 when estimated using mesopelagic traps moored at 500-m depth and by a factor of 3–4 when estimated using surface-tethered drifting traps. When averaged seasonally, flux at BATS was highest in spring (March, April, May) at all depths followed by summer (June, July, August) and decreasing towards fall, but this seasonality was less visible at ESTOC. Seasonal comparison showed the fastest flux attenuation at Bermuda in winter and spring, coinciding with the highest POC flux. POC/PIC ratios derived from the moored traps were significantly higher at BATS than at ESTOC in fall and winter, but this difference was not significant in spring (p>0.05). This study shows that while the western and eastern Atlantic subtropical gyres have similar rates of primary production, the biological carbon pump differs between the two provinces. Higher new nutrient input observed at Bermuda compared to ESTOC might explain part of the difference in export ratio but alone is insufficient. Greater winter mixed-layer depths and higher mesoscale eddy activity at Bermuda resulting in pulsed production events of labile organic matter might explain both the higher export flux and export ratios found at Bermuda.  相似文献   

12.
Temporal variability of acoustically estimated zooplankton biomass at the Bermuda Testbed Mooring (BTM) site in the Sargasso Sea (at 31°43′N, 64°10′W) is described for time scales from less than an hour to the seasonal cycle primarily using data obtained between August 1996 and November 2000, and from May 10 to November 13, 2003. Concurrent high frequency BTM observations of meteorological, physical, and bio-optical variables are used to interpret processes contributing to the zooplankton variability. Zooplankton biomass estimates are derived from regressions of backscatter intensity data measured with an upward looking 153-kHz acoustic Doppler current profiler (ADCP) and zooplankton net tow data collected near the BTM site as part of the Bermuda Atlantic Time-series Study (BATS). Our data show clear event-scale variations. Peaks are associated with annual spring blooms involving mixed layer shoaling and in some cases passages of mesoscale eddy features. Biomass peaks are often coincident with maxima seen in BTM chlorophyll fluorescence measurements (inferred phytoplankton biomass). Some storm events do not appear to manifest in significant perturbations of zooplankton distributions; however, Hurricane Fabian (2003) greatly impacted these distributions. Estimates of zooplankton biomass and relative vertical velocity show the vertical structure of daily migration patterns. Seasonal variations in migration patterns are also evident, with diel changes in zooplankton biomass most pronounced in spring and least pronounced in winter. In summary, our high temporal resolution time series of estimated zooplankton biomass in the open ocean provide information on scales inaccessible through conventional monthly ship-based sampling. These data have implications for upper ocean ecology and the vertical transport of carbon and nitrogen through the diel migration of zooplankton.  相似文献   

13.
The Earth’s most extensive biomes – the oceanic subtropical gyres – are considered to be expanding with current surface ocean warming. Although it is well established that microbial communities control gyre biogeochemistry, comparisons of their metabolic activities between gyres are limited. In order to estimate metabolic activities including production of microbial communities, the uptake rates of amino acids leucine, methionine and tyrosine at ambient concentrations were estimated in surface waters of the Atlantic Ocean using radioisotopically labelled tracers. Data were acquired during six research cruises covering main oceanic provinces herein termed: North and South Atlantic Gyres, Bermuda Atlantic Time-series Study site (BATS), Equatorial region, and Mauritanian Upwelling (off Cape Blanc). Data were divided between provinces, the extents of which were identified by ocean colour data, in order to achieve provincial mean uptake rates. Leucine and methionine uptake rates did not differ between sampling periods, and were comparable between the North and South subtropical gyres. Furthermore, variation in uptake rates measured throughout the two oligotrophic gyres, where sampling covered ∼4 × 106 km2, was considerably lower than that measured within the Mauritanian Upwelling and Equatorial regions, and even at the BATS site. Tyrosine was generally the slowest of the amino acids to be taken up, however, it was assimilated faster than methionine within the Mauritanian Upwelling region. Thus, we propose that one value for leucine (12.6 ± 3.2 pmol L−1 h−1) and methionine (10.0 ± 3.3 pmol L−1 h−1) uptake could be applied to the oligotrophic subtropical gyres of the Atlantic Ocean. However, with the significantly lower uptake rates observed at the BATS site, we would not advise extrapolation to the Sargasso Sea.  相似文献   

14.
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   

15.
Monthly seawater pH and alkalinity measurements were collected between January 1996 and December 2000 at 10°30′N, 64°40′W as part of the CARIACO (CArbon Retention In A Colored Ocean) oceanographic time series. One key objective of CARIACO is to study temporal variability in Total CO2 (TCO2) concentrations and CO2 fugacity (fCO2) at this tropical coastal wind-driven upwelling site. Between 1996 and 2000, the difference between atmospheric and surface ocean CO2 concentrations ranged from about − 64.3 to + 62.3 μatm. Physical and biochemical factors, specifically upwelling, temperature, primary production, and TCO2 concentrations interacted to control temporal variations in fCO2. Air–sea CO2 fluxes were typically depressed (0 to + 10 mmol C m− 2 day− 1) in the first few months of the year during upwelling. Fluxes were higher during June–November (+ 10 to 20 mmol C m− 2 day− 1). Fluxes were generally independent of the slight changes in salinity normally seen at the station, but low positive flux values were seen in the second half of 1999 during a period of anomalously heavy rains and land-derived runoff. During the 5 years of monthly data examined, only two episodes of negative air–sea CO2 flux were observed. These occurred during short but intense upwelling events in March 1997 (−10 mmol C m− 2 day− 1) and March 1998 (− 50 mmol C m− 2 day− 1). Therefore, the Cariaco Basin generally acted as a source of CO2 to the atmosphere in spite of primary productivity in excess of between 300 and 600 g C m− 2 year− 1.  相似文献   

16.
A novel shipboard gas tension device (GTD) that measures total dissolved air pressure in ocean surface waters is described and demonstrated. In addition, an improved method to estimate dissolved N2 levels from simultaneous measurements of gas tension, dissolved O2, water temperature, and salinity is described. Other than a flow-through plenum, the shipboard GTD is similar to the previously described moored-mode GTD (McNeil et al., 1995, Deep-Sea Research I 42, 819–826). The plenum has an integrated water-side screen to protect the membrane, and prevent the membrane from flexing in super-saturated near surface waters. The sampling scheme uses a well mixed and thermally insulated 15 L container that is flushed by the ship's seawater intake at a rate of 3–15 L min−1. Dissolved gas sensors are placed inside this container and flushed with a small recirculation pump. Laboratory data that characterize the response of the modified GTD are presented. The modified GTD has a constant, isothermal, characteristic (e-folding) response time of typically 11±2 min at 20 °C. The response time decreases with increasing temperature and varies by ±35% over a temperature range of 5–35 °C. Results of field measurements, collected on the R.V. Brown between New York and Puerto Rico during September 2002, are presented, and provide the first look at co-variability in surface ocean N2, O2, and CO2 levels over horizontal length scales of several kilometers. Dissolved N2 concentrations decreased by approximately 16% as the ship sailed from the colder northern continental shelf waters, across the Gulf Stream, and into the warmer northwestern Atlantic Ocean. Historical database measurements, buoy time series, and satellite imagery, are used to aid interpretation of the dissolved gas levels.  相似文献   

17.
A global ocean carbon cycle model based on the ocean general circulation model POP and the improved biogeochemical model OCMIP-2 is employed to simulate carbon cycle processes under the historically observed atmospheric CO 2 concentration and different future scenarios (called Rep- resentative Concentration Pathways, or RCPs). The RCPs in this paper follow the design of Inter- governmental Panel on Climate Change (IPCC) for the Fifth Assessment Report (AR5). The model results show that the ocean absorbs CO 2 from atmosphere and the absorbability will continue in the 21st century under the four RCPs. The net air-sea CO 2 flux increased during the historical time and reached 1.87 Pg/a (calculated by carbon) in 2005; however, it would reach peak and then decrease in the 21st century. The ocean absorbs CO 2 mainly in the mid latitude, and releases CO 2 in the equator area. However, in the Antarctic Circumpolar Current (ACC) area the ocean would change from source to sink under the rising CO 2 concentration, including RCP4.5, RCP6.0, and RCP8.5. In 2100, the anthropogenic carbon would be transported to the 40 S in the Atlantic Ocean by the North Atlantic Deep Water (NADW), and also be transported to the north by the Antarctic Bottom Water (AABW) along the Antarctic continent in the Atlantic and Pacific oceans. The ocean pH value is also simulated by the model. The pH decreased by 0.1 after the industrial revolution, and would continue to decrease in the 21st century. For the highest concentration sce- nario of RCP8.5, the global averaged pH would decrease by 0.43 to reach 7.73 due to the absorption of CO 2 from atmosphere.  相似文献   

18.
The seasonal and interannual variability of the air–sea CO2 flux (F) in the Atlantic sector of the Barents Sea have been investigated. Data for seawater fugacity of CO2 (fCO2sw) acquired during five cruises in the region were used to identify and validate an empirical procedure to compute fCO2sw from phosphate (PO4), seawater temperature (T), and salinity (S). This procedure was then applied to time series data of T, S, and PO4 collected in the Barents Sea Opening during the period 1990–1999, and the resulting fCO2sw estimates were combined with data for the atmospheric mole fraction of CO2, sea level pressure, and wind speed to evaluate F.The results show that the Atlantic sector of the Barents Sea is an annual sink of atmospheric CO2. The monthly mean uptake increases nearly monotonically from 0.101 mol C m− 2 in midwinter to 0.656 mol C m− 2 in midfall before it gradually decreases to the winter value. Interannual variability in the monthly mean flux was evaluated for the winter, summer, and fall seasons and was found to be ± 0.071 mol C m− 2 month− 1. The variability is controlled mainly through combined variation of fCO2sw and wind speed. The annual mean uptake of atmospheric CO2 in the region was estimated to 4.27 ± 0.68 mol C m− 2.  相似文献   

19.
Considerable attention has recently been focused on the role of eddies in affecting biogeochemical fluxes and budgets of the Sargasso Sea. In late November 1996, the Bermuda Testbed Mooring (BTM) and Bermuda Atlantic Time Series (BATS) shipboard sampling evidenced a fall phytoplankton bloom at the Bermuda time-series site which was strongly forced by the interplay between seasonal mixed layer destratification and perturbation of mixed layer dynamics due to passage of a warm mesoscale feature. The feature was characterized by clockwise current vector rotation from near the surface to about 200 m and a thick, warm, low salinity isothermal layer >180 m in depth. Nutrients, chlorophyll fluorescence and pigment profiles indicated high primary production stimulated by enhancement of nutrient entrainment and intermittent deep mixing down to the base of the feature's isothermal layer. Nearly coincident with the arrival of this productive feature at the BTM site, the Oceanic Flux Program (OFP) sediment traps recorded an abrupt, factor of 2.5 increase in mass flux at 3200 m depth. Even more dramatic was the observed increase in flux of labile bioreactive organic matter. Fluxes of primary phytoplankton-derived compounds increased by factors of 7–30, bacteria-derived compounds by 6–9, and early degradation products of sterols by a factor of 10. The covariation of early degradation products and bacteria-derived compounds with phytoplankton-derived compounds indicated that the settling phytoplankton bloom material contained elevated bacterial populations and was undergoing active degradation when it entered the 3200 m trap cup.The increase in the flux of bulk components, especially the residual silicate fraction, and refractory organic compounds clearly preceded the main pulse of the labile, surface-derived phytoplankton organic material. The coincident increase in the flux of refractory and zooplankton-derived compounds suggests that in the initial stage of the deep flux event, the mass flux increased largely as a result of an increase in the flux of refractory materials scavenged from the water column and repackaged into sinking particles and increased zooplankton inputs. These results imply that biological reprocessing of flux material within the water column acts to enhance the coupling between the surface and deep ocean environments.Our results show that transient, upper ocean forcing associated with variable upper ocean physical structure—which includes but is not limited to eddies—and variable meteorological forcing can have an enormous effect on the export flux of bioreactive organic material. The importance of pulsed fluxes of bioreactive material arising from transient physical forcing to the long-term average is not presently known. However, the occurrence of episodic high flux events throughout the OFP time-series record (also inferred from BTM time-series) suggests that such forcing, regardless of specific dynamics, may be responsible for a significant fraction of the total export flux of bioreactive carbon and associated elements to the deep oligotrophic ocean.  相似文献   

20.
Remote sensing and surface POC concentration in the South Atlantic   总被引：1，自引：0，他引：1  
Several SeaWiFS products have been compared with shipboard data to assess the possibility of using remote sensing to estimate particulate organic carbon (POC) concentration in surface waters. Transmissometer data were collected during six South Atlantic Ventilation Experiment (SAVE) hydrographic expeditions conducted between November 1987 and March 1989 from R/V Knorr, and Melville. A total of 361 beam attenuation profiles were made with a SeaTech transmissometer interfaced with a CTD/rosette. In order to calculate the POC concentration from transmissometer profiles, a regression between beam attenuation and POC for open Atlantic Ocean waters derived from our research in the North Atlantic (North Atlantic Bloom Experiment, NABE) and enhanced by data from the Bermuda Atlantic Time Series Station (BATS) was applied. The profiles were processed and examined as vertical sections of the surface 250 m. The data were collected in two successive years, during the same season, which allowed us to compile a combined data set over the austral summer for examination. Beam attenuation/POC concentrations were integrated down to one attenuation depth with the intent of making comparisons with satellite optical data. No satellite optical data were available for 1987–1989, so the only option was to compare our integrated data with SeaWiFS-derived variables from later years averaged over the same season as SAVE data. Analysis of four SeaWiFS products acquired from 1997 to 2002 demonstrated very low variations from year to year for seasonally averaged data, suggesting that making comparisons of the beam attenuation/POC fields with averaged satellite optical products from later years is a valid (though not optimal) approach for this area. The highest correlation between beam attenuation/POC concentration and remotely derived products was found with normalized water-leaving radiance at 555 nm. Other SeaWiFS-derived variables—chlorophyll concentration, diffuse attenuation coefficient at 490 nm and integral chlorophyll (integrated over one attenuation depth)—were also compared but showed a slightly less satisfactory correlation.  相似文献   

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