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1.
In January and February 1998, when an unprecedented fourth repetition of the zonal hydrographic transect at 24.5°N in the Atlantic was undertaken, carbon measurements were obtained for the second time in less than a decade. The field of total carbon along this section is compared to that provided by 1992 cruise which followed a similar path (albeit in a different season). Consistent with the increase in atmospheric carbon levels, an increase in anthropogenic carbon concentrations of 8±3 μmolkg−1 was found in the surface layers. Using an inverse analysis to determine estimates of absolute velocity, the flux of inorganic carbon across 24.5° is estimated to be −0.74±0.91 and −1.31±0.99 PgCyr−1 southward in 1998 and 1992, respectively. Estimates of total inorganic carbon flux depend strongly upon the estimated mass transport, particularly of the Deep Western Boundary Current. The 1998 estimate reduces the large regional divergence in the meridional carbon transport suggested by previous studies and brings into question the idea that the tropical Atlantic constantly outgasses carbon, while the subpolar Atlantic sequesters it. Uncertainty in the carbon transports themselves, dominated by the uncertainty in the total mass transport estimates, are a hindrance to determining the “true” picture.The flux of anthropogenic carbon (CANTH) across the two transects is estimated as northward at 0.20±0.08 and 0.17±0.06 PgCyr−1 for the 1998 and 1992 sections, respectively. The net transport of CANTH across 24.5°N is strongly affected by the difference in concentrations between the northward flowing shallow Florida Current and the mass balancing, interior return flow. The net northward transport of CANTH is opposite the net flow of total carbon and suggests, as has been found by others, that the pre-industrial southward transport of carbon within the Atlantic was stronger than it is today. Combining these flux results with estimates of atmospheric and riverine inorganic carbon input, it is determined that today's oceanic carbon system differs from the pre-industrial system in that today there is an uptake of anthropogenic carbon to the south that is advected northward and stored within the North Atlantic basin.  相似文献   

2.
Budgets for conservative tracers are used to determine the flow through the Irish Sea and combined with available data on nutrient distributions and inputs to estimate non-conservative nutrient fluxes. Steady state salinity and caesium-137 balances yield consistent estimates of the flow through the Irish Sea of Φ≈6×104 m3s−1. Using both tracers together with a mass balance allows the inclusion of separate diffusive flux terms and results in a diffusivity estimate ofK≈450 m2s−1and a reduced flow of Φ≈4×104 m3s−1. These values are, however, sensitive to the gradients of salinity and caesium-137 concentration, which are not well defined by the observations.Following the LOICZ procedures, salinity and mass balances were combined with analogous statements for dissolved inorganic phosphorus (DIP) and dissolved inorganic nitrogen (DIN), in order to assess the non-conservative process rates. With regard to phosphorus it was found that the Irish Sea is close to balance with a slight net uptake of dissolved inorganic phosphorus, but the implied excess of uptake over release is not significant on account of uncertainties in the observations of boundary values and inputs. The DIN budget is subject to comparable uncertainties in the input data but does, however, indicate a significant imbalance with an average rate of denitrification of the order 0·3 mol N m−2y−1.The implications of these budget results and their limitations are considered in relation to the application of the budgeting approach to areas with sparse data coverage. While the application of box model disciplines to conservative tracers can lead to satisfactory estimates of advective transport, the extension to non-conservative components requires extensive data to adequately specify the boundary values and input parameters averaged over the seasonal cycle.  相似文献   

3.
Uptake of inorganic carbon and ammonium by the plankton community of three North Carolina estuaries was measured using 14C and 15N isotope methods. At 0% light, C appeared to be lost via respiration, and at increasing light levels uptake of inorganic carbon increased linearly, saturated (mean Ik = 358±30 μEin m−2 s−1), and frequently showed inhibition at the highest light intensities. At 0% light NH4+ uptake was significantly greater than zero and was frequently equivalent to uptake in the light (light independent); at increasing light levels NH4+ uptake saturated (mean Ik = 172±44 μEin m−2 s−1) and frequently indicated strong inhibition. Light-saturated uptake rates of inorganic carbon and NH4+ were a function of chlorophyll a (r2 = 0·7−0·9); average assimilation numbers were 625 nmol CO2 (μg chl. a)−1 h−1 and 12·9 nmol NH4+ (μg chl. a)−1 h−1 and were positively correlated with temperature (r2 = 0·3−0·7). The ratio of dark to light-saturated NH4+ uptake tended to be near 1·0 for large algal populations at low NH4+ concentrations, indicating near light independence of uptake; whereas the ratio was lower for the opposite conditions. These data are interpreted as indicative of nitrogen stress, and it is suggested that uptake of NH4+ deep in the euphotic zone and at night are mechanisms for balancing the C:N of cellular pools. A 24-h study using summed short-term incubations confirmed this; the cumulative C:N of CO2 and NH4+ uptake during the daylight period was 10–20, whereas over the 24-h period the ratio was 6 due to dark NH4+ uptake. Annual carbon and nitrogen primary productivity were respectively estimated as 24 and 4·0 mol m−2 year−1 for the South River estuary, 42 and 7·3 mol m−2 year−1 for the Neuse River estuary, and 9·6 and 1·6 mol m−2 year−1 for the Newport River estuary.  相似文献   

4.
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   

5.
The potential of the North Atlantic as a sink for atmospheric CO2 was investigated by studying the carbonic system using data obtained during the spring of 1991. The air-sea flux of CO2 was related to chlorophyll and other environmental variables, and the regeneration of carbon in the mid-ocean studied by examining vertical sections representative of the study area.Poor correlations were found between pCO2 and chlorophyll throughout much of the study area, although a good correlation was found along 16°W. The highest air-sea fluxes of CO2 were calculated for areas where chlorophyll was highest (45°13′N, 16°04′W), and where the greatest wind speeds occurred (47°51′N, 28°18′W). The mean CO2 flux from the atmosphere to the ocean during the study period (May) was calculated as 0.65mmol m−2d−1, which compares well with other studies. Regression equations were developed to predict total inorganic carbon from nutrients; errors were typically less than 1 μmol kg−1. Regeneration of carbon in the mid-ocean occurred in two principal stages: 0–1000m and>2300m. Regeneration in the upper zone was dominated by soft tissue carbon (86%), with skeletal carbon (calcite) contributing only 14%. The fraction of regenerated carbon of skeletal origin increased to 51% in the>2300m zone.  相似文献   

6.
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   

7.
Rates of net nitrification were calculated for four large (13 m3) estuarine-based microcosms that had been subjected to inorganic nutrient enrichment. Calculated rates were based on two years of weekly nitrate and nitrite measurements and ranged from a maximum of 0·55 μmol NO2+3 produced l−1 day−1 in the control tank (no enrichment) to over 13 μmol NO2+3 produced l−1 day−1 in the most enriched tank (receiving 18·6 μmol NH4 l−1 day−1). Almost all NO2+3 production was pelagic, little was benthic. Net NO3 production or net NO2 production dominated the net nitrification rates during different seasons. Good correlations were found between various oxidation rates and substrate concentrations. The calculated net nitrite production rates were 10 to 1000 times higher than previously reported rates for open ocean systems, demonstrating the potential importance of nitrification to estuarine systems.  相似文献   

8.
Macroalgae biomass and concentrations of nitrogen, phosphorus and chlorophyll a were determined weekly or biweekly in water and sediments, during the spring-summer of 1985 in a hypertrophic area of the lagoon of Venice. Remarkable biomass production (up to 286 g m−2 day−1, wet weight), was interrupted during three periods of anoxia, when macroalgal decomposition (rate: up to 1000 g m−2 day−1) released extraordinary amounts of nutrients. Depending on the macroalgae distribution in the water column, the nutrients released in water varied from 3·3 to 19·1 μg-at litre−1 for total inorganic nitrogen and from 1·8 to 2·7 μg-at litre−1 for reactive phosphorus. Most nutrients, however, accumulated in the surficial sediment (up to 0·640 and to 3·06 mg g−1 for P and N respectively) redoubling the amounts already stored under aerobic conditions, Phytoplankton, systematically below 5 mg m−3 as Chl. a, sharply increased up to 100 mg m−3 only after the release of nutrients in water by anaerobic macroalgal decomposition. During the algal growth periods, the N:P atomic ratio in water decreased to 0·7, suggesting that nitrogen is a growth-limiting factor. This ratio for surficial sediment was between 6·6 and 13·1, similar to that of macroalgae (8·6–12·0).  相似文献   

9.
Rates of transformation, recycling and burial of nitrogen and their temporal and spatial variability were investigated in deep-sea sediments of the Porcupine Abyssal Plain (PAP), NE Atlantic during eight cruises from 1996 to 2000. Benthic fluxes of ammonium (NH4) and nitrate (NO3) were measured in situ using a benthic lander. Fluxes of dissolved organic nitrogen (DON) and denitrification rates were calculated from pore water profiles of DON and NO3, respectively. Burial of nitrogen was calculated from down core profiles of nitrogen in the solid phase together with 14C-based sediment accumulation rates and dry bulk density. Average NH4 and NO3-effluxes were 7.4 ± 19 μmol m−2 d−1 (n = 7) and 52 ± 30 μmol m−2 d−1 (n = 14), respectively, during the period 1996–2000. During the same period, the DON-flux was 11 ± 5.6 μmol m−2 d−1 (n = 5) and the denitrification rate was 5.1 ± 3.0 μmol m−2 d−1 (n = 22). Temporal and spatial variations were only found in the benthic NO3 fluxes. The average burial rate was 4.6 ± 0.9 μmol m−2 d−1. On average over the sampling period, the recycling efficiency of the PON input to the sediment was 94% and the burial efficiency hence 6%. The DON flux constituted 14% of the nitrogen recycled, and it was of similar magnitude as the sum of burial and denitrification. By assuming the PAP is representative of all deep-sea areas, rates of denitrification, burial and DON efflux were extrapolated to the total area of the deep-sea floor (>2000 m) and integrated values of denitrification and burial of 8 ± 5 and 7 ± 1 Tg N year−1, respectively, were obtained. This value of total deep-sea sediment denitrification corresponds to 3–12% of the global ocean benthic denitrification. Burial in deep-sea sediments makes up at least 25% of the global ocean nitrogen burial. The integrated DON flux from the deep-sea floor is comparable in magnitude to a reported global riverine input of DON suggesting that deep-sea sediments constitute an important source of DON to the world ocean.  相似文献   

10.
Spring profiles of microbial production derived from the dark incorporation of tritiated leucine and tritiated thymidine in the northwest Mediterranean show an exponential decline with depth. Assuming this to represent a steady-state balance between microbial respiration and the downward flux of carbon, the downward flux is estimated as (1−/)p/b, where p is the microbial production, their gross growth efficiency and b the coefficient of exponential decline with depth. Summer profiles, ranging over about 3° of latitude and 4° of longitude, were well fitted by a two-component exponential decline, suggesting two distinct microbial substrates. Values of b for the more rapidly declining component varied between 0.01 and 0.06 m−1 according to location. In the case of the slower component, b was estimated as 0.002 m−1, and did not vary significantly over the region. Estimated fluxes of carbon at the surface are 123–335 mg m−2 d−1 for the fast and 95 mg m−2 d−1 for the slow component. Below about 200 m, carbon flux is dominated by the slow component. Flux estimates are compatible with flux estimates from sediment traps in the same region. The observed changes between the spring and summer profiles, combined with the horizontal homogeneity of the summer profiles below 200 m, are consistent with a downward transport of about 5–10 m d–1, implying a significant dispersive component to the observed fluxes.  相似文献   

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