Seasonal and spatial variability in plankton production and respiration in the Subtropical Gyres of the Atlantic Ocean

Euphotic zone plankton production (P) and respiration (R) were determined from the in vitro flux of dissolved oxygen during six latitudinal transects of the Atlantic Ocean, as part of the Atlantic Meridional Transect (AMT) programme. The transects traversed the North and South Atlantic Subtropical Gyres (N gyre, 18–38°N; S gyre, 11–35°S) in April–June and September–November 2003–2005. The route and timing of the cruises enabled the assessment of the seasonal variability of P, R and P/R in the N and S gyres, and the comparison of the previously unsampled N gyre centre with the more frequently sampled eastern edge of the gyre. Mean euphotic zone integrated rates (±SE) were P=63±23 (n=31), R=69±22 (n=30) mmol O₂ m⁻² d⁻¹ in the N gyre; and P=58±26 (n=30), R=62±24 (n=30) mmol O₂ m⁻² d⁻¹ in the S gyre. Overall, the N gyre was heterotrophic (R>P) and it was more heterotrophic than the S gyre, but the metabolic balance of both gyres changed with season. Both gyres were net heterotrophic in autumn, and balanced in spring. This seasonal contrast was most pronounced for the S gyre, because it was more autotrophic than the N gyre during spring. This may have arisen from differences in nitrate availability, because spring sampling in the S gyre coincided with periods of deep mixing to the nitracline, more frequently than spring sampling within the N gyre. Our results indicate that the N gyre is less heterotrophic than previous estimates suggested, and that there is an apparent decrease in R from the eastern edge to the centre of the N gyre, possibly indicative of an allochthonous organic carbon source to the east of the gyre.     

Natural air–sea flux of CO2 in simulations of the NASA-GISS climate model: Sensitivity to the physical ocean model formulation

Results from twin control simulations of the preindustrial CO₂ gas exchange (natural flux of CO₂) between the ocean and the atmosphere are presented here using the NASA-GISS climate model, in which the same atmospheric component (modelE2) is coupled to two different ocean models, the Russell ocean model and HYCOM. Both incarnations of the GISS climate model are also coupled to the same ocean biogeochemistry module (NOBM) which estimates prognostic distributions for biotic and abiotic fields that influence the air–sea flux of CO₂. Model intercomparison is carried out at equilibrium conditions and model differences are contrasted with biases from present day climatologies. Although the models agree on the spatial patterns of the air–sea flux of CO₂, they disagree on the strength of the North Atlantic and Southern Ocean sinks mainly because of kinematic (winds) and chemistry (pCO₂) differences rather than thermodynamic (SST) ones. Biology/chemistry dissimilarities in the models stem from the different parameterizations of advective and diffusive processes, such as overturning, mixing and horizontal tracer advection and to a lesser degree from parameterizations of biogeochemical processes such as gravitational settling and sinking. The global meridional overturning circulation illustrates much of the different behavior of the biological pump in the two models, together with differences in mixed layer depth which are responsible for different SST, DIC and nutrient distributions in the two models and consequently different atmospheric feedbacks (in the wind, net heat and freshwater fluxes into the ocean).     

Distribution of the CO2 partial pressure along an Atlantic meridional transect

Atmospheric and oceanic pCO₂ were measured continuously along an Atlantic Meridional transect (50°N–50°S) in September–October 1995 and 1996 (U.K. to the Falklands Islands) and in April–May 1996 (Falklands Islands to the UK). The Atlantic ocean was a net sink for atmospheric CO₂ for all 3 transects. The largest sinks were located at high latitudes, in regions of high wind speed, where strong CO₂ undersaturations, associated with high biological activity, were observed. In these regions the partial pressure difference between the ocean and the atmosphere reached −110 μatm. A CO₂ source occurred in the equatorial region between 0° and 10°S, where ΔpCO₂ of up to 40 μatm was found. Another source was in the northern subtropical gyre where its extension varied according to the season. Along the whole transect the October cruises exhibited similar pCO₂ distributions suggesting a dominance of the seasonal variability and small year to year changes.     

Prediction of surface ocean pCO2 from observations of salinity, temperature and nitrate: The empirical model perspective

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 (pCO_2SEA) from sea surface salinity (SSS), temperature (SST), and/or nitrate (NO₃) concentration using previously published regional total inorganic carbon (C_T) and total alkalinity (A_T) algorithms. The obtained pCO_2SEA 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 C_T 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 pCO_2SEA predictions. Our analysis indicates that the previously published empirical C_T and A_T models provide reasonable predictions of seasonal variations in surface-water pCO_2SEA within the (sub) tropical oceans based on changes in SSS and SST; however, in high-latitude oceans where ocean biology affects C_T to a significant degree, improved C_T algorithms are required to capture the full biological effect on C_T with greater accuracy and in turn improve the accuracy of predictions of pCO_2SEA.     

Seasonal and interannual variability of oceanic carbon cycling in the western and central tropical-subtropical pacific: A physical-biogeochemical modeling study

The oceanic carbon cycle in the tropical-subtropical Pacific is strongly affected by various physical processes with different temporal and spatial scales, yet the mechanisms that regulate air-sea CO₂ flux are not fully understood due to the paucity of both measurement and modeling. Using a 3-D physical-biogeochemical model, we simulate the partial pressure of CO₂ in surface water (pCO_2sea) and air-sea CO₂ flux in the tropical and subtropical regions from 1990 to 2004. The model reproduces well the observed spatial differences in physical and biogeochemical processes, such as: (1) relatively higher sea surface temperature (SST), and lower dissolved inorganic carbon (DIC) and pCO_2sea in the western than in the central tropical-subtropical Pacific, and (2) predominantly seasonal and interannual variations in the subtropical and tropical Pacific, respectively. Our model results suggest a non-negligible contribution of the wind variability to that of the air-sea CO₂ flux in the central tropical Pacific, but the modeled contribution of 7% is much less than that from a previous modeling study (30%; McKinley et al., 2004). While DIC increases in the entire region SST increases in the subtropical and western tropical Pacific but decreases in the central tropical Pacific from 1990 to 2004. As a result, the interannual pCO_2sea variability is different in different regions. The pCO_2sea temporal variation is found to be primarily controlled by SST and DIC, although the role of salinity and total alkalinity, both of which also control pCO_2sea, need to be elucidated by long-term observations and eddy-permitting models for better estimation of the interannual variability of air-sea CO₂ flux.     

Similarity in microbial amino acid uptake in surface waters of the North and South Atlantic (sub-)tropical gyres

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.     

Interannual variability in the wintertime air–sea flux of carbon dioxide in the northern North Atlantic, 1981–2001

Gridded fields of sea surface temperature (SST), sea level pressure (SLP), and wind speed were used in combination with data for the atmospheric mole fraction of CO₂ and an empirical relationship between measured values of the fugacity of carbon dioxide in surface water and SST, to calculate the air–sea CO₂ flux in the northern North Atlantic. The flux was calculated for each of the months October–March, in the time period 1981 until 2001, allowing for an assessment of the interannual variations in the region. Locally and on a monthly time scale, the interannual variability of the flux could be as high as ±100% in regions seasonally covered by sea ice. However, in open-ocean areas the variability was normally between ±20% and ±40%. The interannual variability was found to be approximately halved when fluxes averaged over each winter season were compared. Summarised over the whole northern North Atlantic, the air to sea carbon flux over winter totalled 0.08 Gton, with an interannual variability of about ±7%. On a monthly basis the interannual variations were slightly higher, about ±8% to ±13%. Changes in wind speed and atmospheric fCO₂ (the latter directly related to SLP variations) accounted for most of the interannual variations of the computed air–sea CO₂ fluxes. A tendency for increasing CO₂ flux into the ocean with increasing values of the NAO index was identified.     

Plankton communities of the South Atlantic anticyclonic gyre

Data collected during cruises of the Former Soviet Union (in 1963–1989) and the British Atlantic meridional transect program (in 1995–1999) were used to analyse macroscale patterns in phyto- and zooplankton biomass, size structure, species diversity, chlorophyll a, and plankton bioluminescence in the macroscale anticyclonic gyre of the South Atlantic Ocean. The spatial pattern of bioluminescence intensity was in good agreement with that of remotely sensed (CZCS) chlorophyll a, phosphate, salinity, and copepod species diversity index distributions especially in terms of geographic inclinations of the isolines, both associated with the north-westward pattern off the South equatorial current. Among the 416 copepod species recorded in samples, 51 species were noted throughout the whole gyre. On the other hand, there were a number of species found only in one of the currents. The mesozooplankton biomass size spectra (calculated in carbon units), exhibited a fairly stable slope of the curve from the eastern periphery of the gyre to its centre. The British Atlantic meridional transect program meridional transect through the western part of the gyre showed mesozooplankton size spectra in greater detail between the equator and 50° S. Although the spectra change slowly along the transect as far as 36° S, there is a general trend toward increasing slopes from the equatorial region to the oligotrophic central gyre. The calculated phyto-to-zooplankton ratio indicated that for the tropical anticyclonic gyres, the mesozooplankton carbon biomass could be represented as the exponential function of the phytoplankton carbon.     

Atlantic meridional overturning circulation and phosphate-classified bottom-up control of Atlantic pelagic ecosystems through the 20th century

Both the Atlantic Meridional Overturning Circulation (AMOC) and the North Atlantic Ocean (NA) biosphere have recognized associations with the North Atlantic Oscillation (NAO). These multidecadal physical–biological affinities inspired a closer look at AMOC influences on bottom-up control of NA and South Atlantic Ocean (SA) pelagic ecosystem variability. Various ocean models associate changes in the AMOC with sea surface temperature (SST) differences in the western subpolar NA and SA represented as the Atlantic Dipole SST Anomaly (ADSA) index. The Extended Reconstructed SST version 2 (ERSSTv2) dataset for 2° quadrangles from 1890 to 2007 was used here to represent Atlantic Ocean SST patterns and to gauge 20th century AMOC variability using an Atlantic Dipole SST (ADS) index, an un-normalized version of ADSA index. Temperature–phosphate (T–PO₄) linear regressions were used to convert temperature to phosphate concentration ([PO₄]). The interannual stability of T–PO₄ linear regressions first was examined using 26 Bermuda area T–PO₄ datasets between 1958 and 2001. Within the constraints provided by the Bermuda analysis, climatological T–PO₄ linear regressions based on GEOSECS-derived slopes and NODC-derived X-intercepts supported the conversion of monthly Atlantic Ocean ERSSTv2 temperatures for each 2° quadrangle to monthly surface [PO₄]. A representative annual surface phosphate utilization (SPU) was calculated for each 2° quadrangle by subtracting monthly minimum surface [PO₄] from monthly maximum surface [PO₄] to determine the annual surface [PO₄] ranges from 1890 to 2007. Annual average SST tended to increase and overall annual average SPU tended to decrease through the 20th century in both the NA and SA, but the NA exhibited more temporal variability. An Atlantic Dipole Phosphate Utilization (ADPU) index related to the ADS index was calculated for each year from 1890 to 2007. The ADS and ADPU indices were inversely correlated with about 57% of the variability in the ADPU index explained by the ADS index. The ADPU index exhibited three distinct cycles through the 20th century. Cross-correlation analysis showed that the NAO led the ADS and ADPU indices by about 14 years. Differences in annual average SPU for each Atlantic Ocean 2° quadrangle between the three high and four low years of the ADPU cycles yielded six maps that, when averaged, clearly exhibited reversed east–west patterns distributed in alternating latitudinal bands in both the NA and SA. The east–west patterns spatially corresponded to the NA and SA surface circulation and temporally resembled NA patterns previously associated with the NAO. AMOC variability, mediated by Kelvin and Rossby waves associated with changes in both deep and surface arm circulation, likely contributed to meridional continuity of phosphate-classified, NA, and SA pelagic ecosystem variability, including fisheries, through the 20th century. Based on the results, future global warming influences on the AMOC, well short of shutdown, likely will have complex pelagic ecosystem impacts throughout the Atlantic Ocean.     

North Pacific Intermediate Water: Progress in SAGE (SubArctic Gyre Experiment) and Related Projects

We survey the recent progress in studies of North Pacific Intermediate Water (NPIW) in SAGE (SubArctic Gyre Experiment), including important results obtained from related projects. Intensive observations have provided the transport distributions relating to NPIW and revealed the existence of the cross-wind-driven gyre Oyashio water transport that flows directly from the subarctic to subtropical gyres through the western boundary current as well as the diffusive contribution across the subarctic front. The anthropogenic CO₂ transport into NPIW has been estimated. The northern part of NPIW in the Transition Domain east of Japan is transported to the Gulf of Alaska, feeding the mesothermal (intermediate temperature maximum) structure in the North Pacific subarctic region where deep convection is restricted by the strong halocline maintained by the warm and salty water transport originating from NPIW. This heat and salt transport is mostly balanced by the cooling and freshening in the formation of dense shelf water accompanied by sea-ice formation and convection in the Okhotsk Sea. Intensive observational and modeling studies have substantially altered our view of the intermediate-depth circulation in the North Pacific. NPIW circulations are related to diapycnal-meridional overturning, generated around the Okhotsk Sea due to tide-induced diapycnal mixing and dense shelf water formation accompanied by sea-ice formation in the Okhotsk Sea. This overturning circulation may possibly explain the direct cross-gyre transport through the Oyashio along the western boundary from the subarctic to subtropical gyres. This revised version was published online in July 2006 with corrections to the Cover Date.     

The contribution of atmospheric acid deposition to ocean acidification in the subtropical North Atlantic Ocean

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.     

On the total geostrophic circulation of the pacific ocean: flow patterns, tracers, and transports

The large-scale circulation of the Pacific Ocean consists of two great anticyclonic gyres that contract poleward at increasing depth, two high-latitude cyclonic gyres, two westward flows along 10° to 15° north and south that are found from the surface to abyssal depths, and an eastward flow that takes place just north of the equator at the surface and at about 500m, but lies along the equator at all other depths.This pattern is roughly symmetric about the equator except for the northward flow across the equator in the west and the southward flow in the east.As no water denser than about 26.8 in σ₀ is formed in the North Pacific, the denser waters of the North Pacific are dominated by the inflow from the South Pacific. Salinity and oxygen in the deeper water are higher in the South Pacific and the nutrients are lower. These characteristics define recognizable paths as they move northward across the equator in the west and circulate within the North Pacific. Return flow is seen across the equator in the east. Part of it turns westward and then southward with the southward limb of the extended cyclonic gyre, and part continues southward along the eastern boundary and through the Drake Passage.The important differences from earlier studies are that the equatorial crossings and the deep paths of flow are defined, and that there are strong cyclonic gyres in the tropics on either side of the equator.     

Hydrography of chromophoric dissolved organic matter in the North Atlantic

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.     

Argo floats revealing bimodality of large-scale mid-depth circulation in the North Atlantic

Analysis of Argo float trajectories at 1 000 m and temperature at 950 m in the North Atlantic between November 2003 and January 2005 demonstrates the existence of two different circulation modes with fast transition between them. Each mode has a pair of cyclonic - anticyclonic gyres. The difference is the location of the cyclonic gyre. The cyclonic gyre stretches from southeast to northwest in the first mode and from the southwest to the northeast in the second mode. The observed modes strongly affect the heat and salt transport in the North Atlantic. In particular, the second mode slows down the westward transport of the warm and saline water from the Mediterranean Sea.     

High-resolution measurement of Southern Ocean CO2 and O2/Ar by membrane inlet mass spectrometry

This paper evaluates the simultaneous measurement of dissolved gases (CO₂ and O₂/Ar ratios) by membrane inlet mass spectrometry (MIMS) along the 180° meridian in the Southern Ocean. The calibration of pCO₂ measurements by MIMS is reported for the first time using two independent methods of temperature correction. Multiple calibrations and method comparison exercises conducted in the Southern Ocean between New Zealand and the Ross Sea showed that the MIMS method provides pCO₂ measurements that are consistent with those obtained by standard techniques (i.e. headspace equilibrator equipped with a Li–Cor NDIR analyser). The overall MIMS accuracy compared to Li–Cor measurements was 0.8 μatm. The O₂/Ar ratio measurements were calibrated with air-equilibrated seawater standards stored at constant temperature (0 ± 1 °C). The reproducibility of the O₂/Ar standards was better than 0.07% during the 9 days of transect between New Zealand and the Ross Sea.The high frequency, real-time measurements of dissolved gases with MIMS revealed significant small-scale heterogeneity in the distribution of pCO₂ and biologically-induced O₂ supersaturation (ΔO₂/Ar). North of 65°S several prominent thermal fronts influenced CO₂ concentrations, with biological factors also contributing to local variability. In contrast, the spatial variation of pCO₂ in the Ross Sea gyre was almost entirely attributed to the biological utilization of CO_2, with only small temperature effects. This high productivity region showed a strong inverse relationship between pCO₂ and biologically-induced O₂ disequilibria (r² = 0.93). The daily sea air CO₂ flux ranged from − 0.2 mmol/m² in the Northern Sub-Antarctic Front to − 6.4 mmol/m² on the Ross Sea shelves where the maximum CO₂ influx reached values up to − 13.9 mmol/m². This suggests that the Southern Ocean water (south of 58°S) acts as a seasonal sink for atmospheric CO₂ at the time of our field study.     

Thermostads and circulation in the upper layer of the Atlantic Ocean

There are three major permanent thermostads with roughly the same potential densities in the upper layer of the Atlantic Ocean. One is the thermostad of the 13°C Water in the equatorial Atlantic. The original type of the 13°C Water is formed in the thermocline in the eastern sector of the South Atlantic subtropical gyre by vertical mixing of dense, low-salinity water from the winter outcrop farther south and overlying less dense, high-salinity water. There might also be a lateral contribution of relatively high-salinity water from the Indian Ocean. The original 13°C Water thus formed is transported northwestward along the northern edge of the subtropical gyre and fed into the North Brazilian Current, which flows equatorward along the coast of Brazil. In the region of the equator, the Equatorial Undercurrent and the subsurface North and South Equatorial countercurrents branch off from the North Brazilian Current and carry the 13°C Water eastward to the thermostad region. Vertical mixing does not explain the development of the thermostad, but is found to be essential in determining the ultimate characteristics of the 13°C Water. The other two thermostads are those of the 18°C Water in the Sargasso Sea and the Subantarctic Mode Water in the western South Atlantic. Unlike the 13°C Water, both of these mode waters are formed as thermostads in the surface layer by winter convection, but vertical mixing in the subtropical gyres may play a role in determining their characteristics. All the three thermostads appear to be required to balance the system of flows in opposing directions.     

The continental shelf pump for CO2 in the North Sea—evidence from summer observation

Data on the distribution of dissolved inorganic carbon (DIC) and partial pressure of CO₂ (pCO₂) were obtained during a cruise in the North Sea during late summer 2001. A 1° by 1° grid of 97 stations was sampled for DIC while the pCO₂ was measured continuously between the stations. The surface distributions of these two parameters show a clear boundary located around 54°N. South of this boundary the DIC and pCO₂ range from 2070 to 2130 μmol kg⁻¹ and 290 to 490 ppm, respectively, whereas in the northern North Sea, values range between 1970 and 2070 μmol kg⁻¹ and 190 to 350 ppm, respectively. The vertical profiles measured in the two different areas show that the mixing regime of the water column is the major factor determining the surface distributions. The entirely mixed water column of the southern North Sea is heterotrophic, whereas the surface layer of the stratified water column in the northern North Sea is autotrophic. The application of different formulations for the calculation of the CO₂ air–sea fluxes shows that the southern North Sea acts as a source of CO₂ for the atmosphere within a range of +0.8 to +1.7 mmol m⁻² day⁻¹, whereas the northern North Sea absorbs CO₂ within a range of −2.4 to −3.8 mmol m⁻² day⁻¹ in late summer. The North Sea as a whole acts as a sink of atmospheric CO₂ of −1.5 to −2.2 mmol m⁻² day⁻¹ during late summer. Compared to the Baltic and the East China Seas at the same period of the year, the North Sea acts a weak sink of atmospheric CO₂. The anticlockwise circulation and the short residence time of the water in the North Sea lead to a rapid transport of the atmospheric CO₂ to the deeper layer of the North Atlantic Ocean. Thus, in late summer, the North Sea exports 2.2×10¹² g C month⁻¹ to the North Atlantic Ocean via the Norwegian trench, and, at the same period, absorbs from the atmosphere a quantity of CO₂ (0.4 10¹² g C month⁻¹) equal to 15% of that export, which makes the North Sea a continental shelf pump of CO₂.     

全球海洋环流模式中上层海洋对表面强迫的响应和调整Ⅱ.年代际变率

利用一个较高分辨率的全球海洋环流模式在COADS 1945～1993年逐月平均资料的强迫下对海温和环流场进行了模拟,分析了北太平洋海温和环流场的年代际变化特征,同时诊断了1976-77年代际跃变过程中海温场变化的机制.模式模拟出了北太平洋海温年代际异常的主要模态以及1976-77年跃变前后的演变特征,模拟的北太平洋中部、加州沿岸和KOE区的海温异常的强度和演变趋势均和观测比较一致;同时,模式重现了分别始于20世纪70和80年代的中纬度海温异常信号沿等密度面向低纬地区的两次潜沉过程.在表层,流场的异常主要表现为与风应力异常基本符合Ekman关系的一个异常海洋涡旋,而整个上层海洋平均的流场异常则表现为两个海洋涡旋的异常,其中副热带海洋涡旋的异常的强度要显著于副极地海洋涡旋的异常,而副极地海洋涡旋异常出现的时间比副热带海洋涡旋晚3a左右的时间.对1976-77年前后3个区域上层海温各贡献项的诊断结果表明,北太平洋中部变冷主要是水平平流和热通量异常贡献的结果;而加州沿岸变暖主要归因于热通量的贡献;在KOE区,垂直平流、热通量和水平平流三者都起了重要作用,其中水平平流异常对这一区域海温年代际跃变出现的时间起了至关重要的作用.     

Primary production and chlorophyll distributions in the subtropical and tropical waters of the Atlantic Ocean in the autumn of 2002

In October and November 2002, high and relatively high values of the chlorophyll a concentration at the sea surface (C _chl) were observed in the English Channel (0.47 mg/m³), in the waters of the North Atlantic Current (0.25 mg/m³), in the tropical and subtropical anticyclonic gyres (0.07–0.42 mg/m³), and also in the southwestern region of the southern subtropical anticyclonic gyre (usually 0.11–0.23 mg/m³). The central regions of the southern subtropical anticyclonic gyre (SATG) and the North Atlantic tropical gyre (NATR) were characterized by lower values of C _chl (0.02–0.08 mg/m³ for the SATG and 0.07–0.14 mg/m³ for the NATR). At most of the SATG stations, the values of the surface primary production (C _phs) varied from 2.5 to 5.5 mg C/m³ per day and were mainly defined by the fluctuations of C _chl (r = +0.78) rather than by those of the assimilation number (r = +0.54). The low assimilation activity of phytoplankton in these waters (1.3–4.6 mg chl a per hour) pointed to a lack of nutrients. An analysis of the variability of their concentration and the composition of photosynthetic pigments showed that, in the waters north of 30° N, the growth of phytoplankton was mostly restricted by the deficiency of nitrogen, while, in more southern areas, at the majority of stations (about 60%), the phosphorus concentrations were the minimum. At the low concentrations of nitrates and nitrites, ammonium represented itself as a buffer that prevented planktonic algae from extreme degrees of nitric starvation. In the tropical waters and in the waters of the SATG, the primary production throughout the water column varied from 240 to 380 mg C/m² 30° per day. This level of productivity at stations with low values of C _chl (<0.08 mg/m³) was provided by a well-developed deep chlorophyll maximum and a high transparency of the water. The light curves of photosynthesis based on in situ measurements point to the high efficiency of utilizing the penetrating solar radiation by phytoplankton on cloudy days.     

Latitudinal Distribution of CO2 Fugacity along 175°E in the North Pacific in 1992–1996

In order to examine latitudinal distribution and seasonal change of the surface oceanic fCO₂, we analyzed the data obtained in the North Pacific along 175°E during the NOPACCS cruises in spring and summer of 1992–1996. Except for around the equator where the fCO₂ was significantly affected by the upwelling of deep water, the latitudinal distribution of fCO₂ showed distinctive seasonal variation. In the spring, the fCO₂ decreased and then increased going southward with the minimum value of about 300 µatm around 35°N, while in the summer, the fCO₂ displayed high variability, showing minimum and maximum values at latitudes of around 44° and 35°N, respectively. It was also found that the fCO₂ was well correlated with the SST, but the relationship between the two was different for different hydrographic regions. In the subpolar gyre, the frontal regions between the Water-Mass Front and the Kuroshio bifurcation front, and between the Kuroshio bifurcation front and the Kuroshio Extension current, SST, DIC and TA influenced the seasonal fCO₂ change through seasonally-dependent biological activities and vertical mixing and stratification of seawater. In the central subtropical gyre and the North Equatorial current, the seasonal fCO₂ change was found to be produced basically by changes in SST and DIC. The summertime oceanic fCO₂ generally increased with time over the period covered by this study, but the increased rate was clearly higher than those expected from other measurements in the western North Pacific.