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1.
Photorefractive properties of Hf:Fe:LiNbO3 crystals with various [Li]/[Nb] ratios have been investigated at 488 nm wavelength based on the two-wave coupling experiment. High diffraction efficiency and large recording sensitivity are observed and explained. The decrease in Li vacancies is suggested to be the main contributor to the increase in the photoconductivity and subsequently to the induction of the improvement of recording sensitivity. The saturation diffraction efficiency is measured up to 80.2%, and simultaneously the recording sensitivity of 0.91 cm/J is achieved to in the Hf:Fe:LiNbO3 crystal grown from the melt with the [Li]/[Nb] ratio of 1.20, which is significantly enhanced as compared with those of the Hf:Fe:LiNbO3 crystal with the [Li]/[Nb] ratio of 0.94 in melt under the same experimental conditions. Experimental results definitely show that increasing the [Li]/[Nb] ratio in crystal is an effective method for Hf:Fe:LiNbO3 crystal to improve its photorefractive properties.  相似文献   

2.
Wyville Thomson Ridge Overflow Water (WTOW), which is the only part of the outflow from the Norwegian Sea not to directly enter the Iceland Basin, is shown to be a significant water mass in the northern Rockall Trough. It is found primarily at intermediate depths (600–1200 m) beneath the northward flowing warm Atlantic waters, and above recirculating Mediterranean influenced waters and Labrador Sea Water (LSW). The bottom of the WTOW layer can be identified by a mid-depth inflexion point in potential temperature–salinity plots. An analysis of historical data reveals that WTOW has been present in all but eight of the last 31 years at 57.5°N in the Rockall Trough. A denser component of WTOW below 1500 m has also been present, although it appears to be less persistent (12 out of the 31 years) and limited to the west of the section. The signature of intermediate WTOW was absent in two periods, the mid-1980s and early 1990s, both of which coincided with a freshening, and probable increase in volume, of LSW in the trough. Potential temperature–salinity diagrams from historical observations indicate that WTOW persists at least as far south as 55°N (and as far west as 20°W in the Iceland Basin) although its signature is quickly lost on leaving the Rockall Trough. We suggest that a transport of WTOW down the western side of the trough exists, with WTOW at intermediate depths entering the eastern trough either via a cyclonic recirculation, or as a result of eddy activity. Further, WTOW is seen on the Rockall–Hatton Plateau and in the deep channels connecting with the Iceland Basin, suggesting additional possible WTOW transport pathways. These suggested transport routes remain to be confirmed by further observational or modelling studies.  相似文献   

3.
Dissolved Fe, Mn and Al concentrations (dFe, dMn and dAl hereafter) in surface waters and the water column of the Northeast Atlantic and the European continental shelf are reported. Following an episode of enhanced Saharan dust inputs over the Northeast Atlantic Ocean prior and during the cruise in March 1998, surface concentrations were enhanced up to 4 nmol L− 1 dFe, 3 nmol L− 1 dMn and 40 nmol L− 1 dAl and returned to 0.6 nmol L− 1 dFe, 0.5 nmol L− 1 dMn and 10 nmol L− 1 dAl towards the end of the cruise three weeks later. A simple steady state model (MADCOW, [Measures, C.I., Brown, E.T., 1996. Estimating dust input to the Atlantic Ocean using surface water aluminium concentrations. In: Guerzoni. S. and Chester. R. (Eds.), The impact of desert dust across the Mediterranean, Kluwer Academic Publishers, The Netherlands, pp. 301–311.]) was used which relies on surface ocean dAl as a proxy for atmospheric deposition of mineral dust. We estimated dust input at 1.8 g m− 2 yr− 1 (range 1.0–2.9 g m− 2 yr− 1) and fluxes of dFe, dMn and dAl were inferred. Mixed layer steady state residence times for dissolved metals were estimated at 1.3 yr for dFe (range 0.3–2.9 yr) and 1.9 yr for dMn (range 1.0–3.8 yr). The dFe residence time may have been overestimated and it is shown that 0.2–0.4 yr is probably more realistic. Using vertical dFe versus Apparent Oxygen Utilization (AOU) relationships as well as a biogeochemical two end member mixing model, regenerative Fe:C ratios were estimated respectively to be 20 ± 6 and 22 ± 5 μmol Fe:mol C. Combining the atmospheric flux of dFe to the upper water column with the latter Fe:C ratio, a ‘new iron’ supported primary productivity of only 15% (range 7%–56%) was deduced. This would imply that 85% (range 44–93%) of primary productivity could be supported by regenerated dFe. The open ocean surface data suggest that the continental shelf is probably not a major source of dissolved metals to the surface of the adjacent open ocean. Continental shelf concentrations of dMn, dFe, and to a lesser extent dAl, were well correlated with salinity and express mixing of a fresher continental end member with Atlantic Ocean water flowing onto the shelf. This means probably that diffusive benthic fluxes did not play a major role at the time of the cruise.  相似文献   

4.
A time series of a standard hydrographic section in the northern Rockall Trough spanning 23 yr is examined for changes in water mass properties and transport levels. The Rockall Trough is situated west of the British Isles and separated from the Iceland Basin by the Hatton and Rockall Banks and from the Nordic Seas by the shallow (500 m) Wyville–Thompson ridge. It is one pathway by which warm North Atlantic upper water reaches the Norwegian Sea and is converted into cold dense overflow water as part of the thermohaline overturning in the northern North Atlantic and Nordic Seas. The upper water column is characterised by poleward moving Eastern North Atlantic Water (ENAW), which is warmer and saltier than the subpolar mode waters of the Iceland Basin, which also contribute to the Nordic Sea inflow. Below 1200 m the deep Labrador Sea Water (LSW) is trapped by the shallowing topography to the north, which prevents through flow but allows recirculation within the basin. The Rockall Trough experiences a strong seasonal signal in temperature and salinity with deep convective winter mixing to typically 600 m or more and the formation of a warm fresh summer surface layer. The time series reveals interannual changes in salinity of ±0.05 in the ENAW and ±0.04 in the LSW. The deep water freshening events are of a magnitude greater than that expected from changes in source characteristics of the LSW, and are shown to represent periodic pulses of newer LSW into a recirculating reservior. The mean poleward transport of ENAW is 3.7 Sv above 1200 dbar (of which 3.0 Sv is carried by the shelf edge current) but shows a high-level interannual variability, ranging from 0 to 8 Sv over the 23 yr period. The shelf edge current is shown to have a changing thermohaline structure and a baroclinic transport that varies from 0 to 8 Sv. The interannual signal in the total transport dominates the observations, and no evidence is found of a seasonal signal.  相似文献   

5.
A 700 km wide-angle reflection/refraction profile carried out in the central North Atlantic west of Ireland crossed the Erris Trough, Rockall Trough and Rockall Bank, and terminated in the western Hatton-Rockall Basin. The results reveal the presence of a number of sedimentary basins separated by basement highs. The Rockall Trough, with a sedimentary pile up to 5 km thick, is underlain by thinned continental crust 8–10 km thick. Some major fault block structures are identified, especially on the eastern margin of the Rockall Trough and in the adjacent Erris Trough. The Hatton-Rockall Basin is underlain by westward-thinning continental crust 22–10 km thick. Sedimentary strata are up to 5 km thick. The strata in the Rockall Trough and Hatton-Rockall Basin probably range in age from Late Palaeozoic to Cenozoic. However, the basins have different sedimentation histories and differ in structural style. The geometry of the crust and sediments suggests that the Rockall Trough originated by pure shear crustal stretching, associated with rift deposits and Cenozoic thermal sag strata. In contrast, the development of the Erris Trough, located on unthinned continental crust, was facilitated by shallow, brittle extension with little deep crustal attenuation. A two-layered crust occurs throughout the region. The lower crustal velocity in the Hatton-Rockall Basin is higher than that in the Rockall Trough. The velocity structure shows no indication of crustal underplating by upper mantle material in the region.  相似文献   

6.
We report measurements of dissolved iron (dFe, <0.4 μm) in seawater collected from the upper 300 m of the water column along the CLIVAR SR3 section south of Tasmania in March 1998 (between 42°S and 54°S) and November–December 2001 (between 47°S and 66°S). Results from both cruises indicate a general north-to-south decrease in mixed-layer dFe concentrations, from values as high as 0.76 nM in the Subtropical Front to uniformly low concentrations (<0.1 nM) between the Polar Front and the Antarctic continental shelf. Samples collected from the seasonal sea-ice zone in November–December 2001 provide no evidence of significant dFe inputs from the melting pack ice, which may explain the absence of pronounced ice-edge algal blooms in this sector of the Southern Ocean, as implied by satellite ocean-color images. Our data also allow us to infer changes in the dFe concentration of surface waters during the growing season. South of the Polar Front, a comparison of near-surface with subsurface (150 m depth) dFe concentrations in November–December 2001 suggests a net seasonal biological uptake of at least 0.14–0.18 nM dFe, of which 0.05–0.12 nM is depleted early in the growing season (before mid December). A comparison of our spring 2001 and fall 1998 data indicates a barely discernible seasonal depletion of dFe (0.03 nM) within the Polar Frontal Zone. Further north, most of our iron profiles do not exhibit near-surface depletions, and mixed-layer dFe concentrations are sometimes higher in samples from fall 1998 compared to spring 2001; here, the near-surface dFe distributions appear to be dominated by time-varying inputs of aerosol iron or advection of iron-rich subtropical waters from the north.  相似文献   

7.
The first iron (Fe) – fertilization experiment in the western North Pacific was carried out using SF6 to trace the Fe-fertilized water mass. A solution in 10,800 liters of seawater of 350 kg of Fe and 0.48 M of SF6 tracer was released into the mixed layer over a 8 × 10 km area. On the first underway transects through the patch after the Fe release, we observed a significant increase of dissolved Fe (ave. 2.89 nM). The fertilized patch was traced for 14 days by on-board SF6 analysis. A Lagrangian frame of reference was maintained by the use of a drogued GPS buoy released at the center of the patch. The patch moved westward at a rate of 6.8 km d−1. Mixed layer depth increased from 8.5 to 15 m during the experiment. Horizontal diffusivity was determined by the change of SF6 concentration in the patch. The horizontal diffusivity increased during the experiment. We evaluate here the fate of Fe in a Fe-fertilized patch using the dilution rate determined from sulphur hexafluoride (SF6) concentration. Dissolved Fe concentrations subsequently decreased rapidly to 0.15 nM on Day 13. However, the dissolved Fe half-life of 43 h was relatively longer than in previous Fe-enrichment studies, and we observed a larger increase of the centric diatom standing stock and corresponding drawdown of macro-nutrients and carbon dioxide than in the previous studies. The most important reason for the larger response was the phytoplankton species in the western North Pacific. In addition, the smaller diffusivity and shallower mixed layer were effective to sustain the higher dissolved Fe concentration compared to previous experiments. This might be one reason for the larger response of diatoms in SEEDS.  相似文献   

8.
The role of Mediterranean Overflow Water (MOW) in creating subsurface salinity anomalies within the Rockall Trough, a gateway to high latitude areas of deep convection, has been examined closely in recent years. Eulerian investigations of high latitude property fields have suggested that these subsurface anomalies are likely the result of variability in the zonal extent of the eastern limb of the subpolar gyre: when expanded into the eastern North Atlantic, the gyre is presumed to limit the extent to which MOW is able to penetrate northward to subpolar latitudes. However, though the depth of the subsurface salinity anomalies in the Rockall Trough supports the hypothesis that the intermittent presence of MOW is involved in creating the anomalies, MOW pathways to the Rockall Trough have not yet been established. Here, Lagrangian trajectories from floats released in the eastern North Atlantic between 1996 and 1997 and synthetic trajectories launched within an eddy-resolving ocean general circulation model are used to demonstrate that two main density neutral transport pathways lead to the Rockall Trough. One pathway involves the transport of relatively fresh waters as part of the North Atlantic Current and the other involves the transport of relatively salty waters from the eastern reaches of the subtropical North Atlantic. The results from this study indicate that changes in these pathways over time can explain the subsurface salinity variability in the Rockall Trough.  相似文献   

9.
The chemical speciation of dissolved mercury in surface waters of Galveston Bay was determined using the concentrations of mercury-complexing ligands and conditional stability constants of mercury-ligand complexes. Two classes of natural ligands associated with dissolved organic matter were determined by a competitive ligand exchange-solvent solvent extraction (CLE-SSE) method: a strong class (Ls), ranging from 19 to 93 pM with an average conditional stability constant (KHgLs) of 1028, and a weak class (Lw) ranging from 1.4 to 9.8 nM with an average KHgLs of 1023. The range of conditional stability constants between mercury and natural ligands suggested that sulfides and thiolates are important binding sites for dissolved mercury in estuarine waters. A positive correlation between the estuarine distribution of dissolved glutathione and that of mercury-complexing ligands supported this suggestion. Thermodynamic equilibrium modeling using stability constants for HgL, HgClx, Hg(OH)x, and HgCl(OH) and concentrations of each ligand demonstrated that almost all of the dissolved mercury (> 99%) in Galveston Bay was complexed by natural ligands associated with dissolved organic matter. The importance of low concentrations of high-affinity ligands that may originate in the biological system (i.e., glutathione and phytochelatin) suggests that the greater portion of bulk dissolved organic matter may not be important for mercury complexation in estuarine surface waters.  相似文献   

10.
Measurements of zinc and zinc complexation by natural organic ligands in the northeastern part of the Atlantic Ocean were made using cathodic stripping voltammetry with ligand competition. Total zinc concentrations ranged from 0.3 nM in surface waters to 2 nM at 2000 m for open-ocean waters, whilst nearer the English coast, zinc concentrations reached 1.5 nM in the upper water column. In open-ocean waters zinc speciation was dominated by complexation to a natural organic ligand with conditional stability constant (log KZnL′) ranging between 10.0 and 10.5 and with ligand concentrations ranging between 0.4 and 2.5 nM. The ligand was found to be uniformly distributed throughout the water column even though zinc concentrations increased with depth. Organic ligand concentrations measured in this study are similar to those published for the North Pacific. However the log KZnL′ values for the North Atlantic are almost and order of magnitude lower than those reported by Bruland [Bruland, K.W., 1989. Complexation of zinc by natural organic-ligands in the central North Pacific. Limnol. Oceanogr., 34, 269–285.] using anodic stripping voltammetry for the North Pacific. Free zinc ion concentrations were low in open-ocean waters (6–20 pM) but are not low enough to limit growth of a typical oceanic species of phytoplankton.  相似文献   

11.
The Wyville Thomson Ridge forms part of the barrier to the meridional circulation across which cold Nordic Sea and Arctic water must traverse to reach the Atlantic Ocean. Overflow rates across the ridge are variable (but can be dramatic at times), and may provide a subtle indicator of significant change in the circulation in response to climate change. In spring 2003, a series of CTD sections were conducted during a large overflow event in which Norwegian Sea Deep Water (NSDW) cascaded down the southern side of the ridge into the Rockall Trough at a rate of between 1 and 2 Sv. The NSDW was partially mixed with overlying North Atlantic Water (NAW), and comprised about 1/3rd of the cascading water. The components of NAW and NSDW in the overflow were sufficiently large that there must have been a significant divergence of the inflow through the Faroe-Shetland Channel, and of the outflow through the Faroe Bank Channel.As the plume descended, its temperature near the sea bed warmed by over 3 °C in about a day. Although the slope was quite steep (0.03), the mean speed of the current (typically 0.36 m s−1) was too slow for significant entrainment of NAW to occur (the bulk Richardson number was of order 5). However, very large overturns (up to 50 m) were evident in some CTD profiles, and it is demonstrated from Thorpe scale estimates that the warming of the bottom waters was due to mixing within the plume. It is likely that some of the NSDW had mixed with NAW before it crossed the ridge. The overflow was trapped in a gully, which caused it to descend to great depth (1700 m) at a faster rate, and with less modification due to entrainment, than other overflows in the North Atlantic. The water that flowed into the northern part of the Rockall Trough had a temperature profile that ranged from about 3 to 8 °C. Water with a temperature of >6 °C probably escaped into the Iceland Basin, between the banks that line the north-western part of the Trough. Colder water (< 6 °C) must have travelled down the eastern side of the Rockall Bank, and may have had a volume flux of up to 1.5 Sv.  相似文献   

12.
Between 1996 and the mid-2000s the upper waters (200–700 m) of the Rockall Trough became warmer (+0.72 °C), saltier (+0.088) and reduced in nitrate and phosphate (−2.00 µM and −0.14 µM respectively). These changes, out-with calculated errors, can be explained by the varying influence of southern versus subpolar water masses in the basin as the Subpolar Gyre weakened and contracted. Upper water properties strongly correlate with a measure of the strength of the Subpolar Gyre (the first principal component of sea surface height over the Subpolar North Atlantic) prior to the mid-2000s. As the gyre weakens, the upper layers of the trough become warmer (r−0.85), more saline (r−0.86) and reduced in nitrate and phosphate (r+0.81 and r+0.87 respectively). Further the proportion of subpolar waters in the basin decreases from around 50% to less than 20% (r+0. 88). Since the mid−2000s the Subpolar Gyre has been particularly weak. During this period temperatures decreased slightly (−0.21 °C), salinities remained near constant (35.410±0.005) and phosphate levels low and stable (0.68±0.02 µM). These relative lack of changes are thought to be related to the maximum proportion of southern water masses within the Rockall Trough having been reached. Thus the upper water properties are no longer controlled by changes in the relative importance of different water masses in the basin (as prior to the mid-2000s), but rather a different process. We suggest that when the gyre is particularly weak the interannual changes in upper water properties in the Rockall Trough reflect changes in the source properties of the southern water masses. Since the early-2000s the Subpolar Gyre has been weaker than observed since 1992, or modelled since 1960–1970. Hence upper waters within the Rockall Trough may be warmer, saltier and more depleted in nitrate and phosphate than at any time in the last half century.  相似文献   

13.
The saturation of calcite and aragonite in the Arctic Ocean   总被引：1，自引：0，他引：1  
We report on the chemical saturation of CaCO3 in the waters of the Arctic Ocean calculated from total alkalinity (AT) and total dissolved inorganic carbon (CT). Data based on four different expeditions are presented: International Arctic Ocean Expedition (IAOE-91), Arctic Ocean Section 94 (AOS94), Polarstern Arctic '96 expedition (ACSYS 96), and Joint Ocean Ice Study 97 (JOIS 97). The results show a lysocline at around 3500 m for aragonite and that most of the Arctic Ocean sea floor lies above the lysocline for calcite. The only anomaly is the low degree of saturation at the shelf break depth in the Canadian Basin seen in the sections of the AOS94 and JOIS 97 cruises, correlated with nutrient maxima and very low O2 concentration, suggesting decomposition of organic matter. The insignificant variability in degree of saturation between the deep waters of the different basins in the Arctic Ocean indicates a very low sedimentation/remineralisation of organic soft matter.  相似文献   

14.
Iron (Fe) is the limiting nutrient for primary productivity in the Southern Ocean, with much of the dissolved iron (dFe) bound to organic ligands or colloids. A Fe model for the Southern Ocean (SOFe) is developed to understand the role of bacteria and organic ligands in controlling Fe cycling and productivity. The model resolves the classical food web and microbial loop, including three types of nutrients (N, Si, Fe) and two types of Fe ligands. Simulations of the zero-dimensional (0-D) model are calibrated with detailed results of shipboard grow-out incubation experiments conducted with Antarctic Peninsula phytoplankton communities during winter 2006 to provide the best estimate of key biological parameters. Then a one-dimensional (1-D) model is developed by coupling the biological model with the Regional Oceanic Modeling System (ROMS) for a site on the Antarctic Peninsula shelf, and the model parameters are further calibrated with data collected from two surveys (summer 2004 and winter 2006) in the area. The results of the numerical simulations agree reasonably well with observations. An analysis of the 1-D model results suggests that bacteria and organic ligands may play an important role in Fe cycling, which can be categorized into a relatively fast mode within the euphotic zone dominated by photo-reactions (summer d Fe residence time about 600 days) and complexation and a slow mode below with most of the dFe biologically complexed (summer dFe residence time >10 years). The dFe removal from the euphotic zone is dominated by colloidal formation and further aggregations with additional contribution from biological uptake, and an increase of organic ligands would reduce Fe export. The decrease of Fe removal rate over depth is due to the continuous dissolution and remineralization of particulate Fe. A number of sensitivity experiments are carried out for both 0-D and 1-D models to understand the importance of photo-reactive processes in primary productivity, bacterial activity, Fe speciation, and dFe residence time within the euphotic zone. The bio-availability of ligand-bound Fe (FeL) is critical to modeled high primary productivity, which is consistent with both shipboard measurements and field observations. In addition, model productivity is sensitive to photoreaction rates if FeL is not directly available for phytoplankton uptake.  相似文献   

15.
Dissolved Fe and ligand concentrations and the Fe-binding strength of the organic ligands were measured in samples from the upper water column (150 m) of the oligotrophic waters of the Canary Basin (eastern North Atlantic Ocean). Concentrations of major nutrients, phytoplankton abundance and photosynthetic characteristics were also measured in the same samples.The concentrations of dissolved Fe and dissolved organic ligands were low with mean values of 0.31 ± 0.18 nM Fe and 1.79 ± 0.73 nEq of M Fe(n = 47), respectively. The conditional binding constant varied between 1019.8–1022.7 (n = 47). The largest variation with depth in the ligand concentrations (between 4.78 and 1.1 nEq of M Fe) was observed in the upper layer, above the Deep Chlorophyll Maximum (DCM located between 80 and 100 m), with high surface values in stations at 18 and 34.At the DCM where Fe was depleted, the ligand concentrations were still relatively high showing the same trend with depth as the amount of phytoplankton cells. Here 62% of the vertical variation in ligand concentrations can be explained by parameters describing phytoplankton cell abundance or biomass and orthosilicic acid concentration, which could reflect diatom growth. Ligand concentrations below the maximum of the DCM (n = 4) showed good linear positive relationships with the total phytoplankton biomass as well as with 2 out of 4 distinguished groups of phytoplankton (Synechococcus and pico-eukaryote I).In the maximum of the DCM and below this maximum the phytoplankton origin of the dissolved organic ligands of Fe is very probable. Data suggest a release of ligands by cell lysis and not by an active production. However, the origin in the surface layer is more difficult to explain. Although the amount of phytoplankton cells in the surface layer is reduced, it is still  25% of the cell concentration observed in the DCM. High concentrations of organic ligands could then be a remnant of past blooms or present production under nutrient depleted conditions. Input of Sahara dust can be another source of ligands.  相似文献   

16.
The speciation of lead at a site in the South San Francisco Bay was determined using a combination of physical size fractionation and electrochemical analyses. The ‘ total dissolvable ’ Pb was 8·1 nM from analysis of an acidified unfiltered sample. The ‘ dissolved ’ Pb was equal to 0·20 nM (41 ng l−1), only 2·5% of the ‘ total dissolvable ’ Pb. The difference yielded the ‘ particulate ’ Pb equal to 7·9 nM (1·6 μg l−1). Results from crossflow ultrafiltration indicated that almost all (0·19 nM) of the dissolved Pb was ‘ in solution ’ [<10K nominal molecular weight (MW)] and that colloidal Pb (10K MW to 0·2 μm)accounted for onlyc. 1% of the dissolved Pb at this station. This small concentration (0·01 nM) of colloidal Pb may be attributed to the low amount of organic carbon associated with colloid size fraction as determined by dissolved organic carbon analyses.The chemical speciation of lead was determined in the dissolved sample and ultrafiltered sub-sample. Differential pulse anodic stripping voltammetry (DPASV) on a thin mercury film (TMF) rotating glassy carbon disk electrode (RGCDE) was used to distinguish the kinetically labile inorganic species (Pb′) from the Pb-chelated by organic ligands (PbLi). Lead titration results were similar for both samples revealing that Pb′, PbLiand excess unbound ligands were present primarily in the ultrafiltrate, rather than in the colloidal phase. The titration data can be interpreted as dissolved Pb being influenced by two classes of Pb-binding ligands. In the dissolved sample, the concentration of the stronger class of ligands was [L1]=0·89±0·35 nM, with a conditional stability constant ofKcondL1,Pb′=3±1×1010M−1. The weaker class was [L2]=12·8±1·9 nM, withKcondL1,Pb′=4±1×108 M−1. The presence of these ligands, in excess of the dissolved Pb, resulted in [Pb′]=7±2 pM and [Pb2+]=0·3 pM (62 pg l−1). While less than 2·4% of the ambient Pb was ‘ in solution ’, it existed chiefly in the form of organic complexes with [PbL1]=0·15 nM and [PbL2]=0·03 nM. More significantly, there were large concentrations of unchelated Pb-binding ligands, (Li′), available to buffer the free Pb2+concentration in the event of perturbations in dissolved Pb.  相似文献   

17.
Concentrations of dissolved Al and Fe in the surface mixed layer were measured during five cruises of the 1995 US JGOFS Arabian Sea Process Study, Concentrations of both Al and Fe were relatively uniform between January and April, the NE Monsoon and the Spring Intermonsoon period, ranging from 2 to 11 nM Al (mean 5.3 nM) and 0.5 to 2.4 nM Fe (mean 1.0 nM). In July/August, after the onset of the SW Monsoon, surface water Al and Fe concentrations increased significantly (Al range 4.5–20.1 nM; mean=10 nM, Fe range 0.57–2.4 nM; mean=1.3 nM), particularly in the NE part of the Arabian Sea, as the result of the input and partial dissolution of eolian dust. Using the enrichment of Al in the surface waters, we estimate this is the equivalent to the deposition of 2.2–7.4 g m−2 dust, which is comparable to values previously estimated for this region. Approximately one month later (August/September), surface water concentrations of both Al and Fe were found to have decreased significantly (mean Al 7.4 nM, mean Fe 0.90 nM) particularly in the same NE region, as the result of export of particulate material from the euphotic zone. Fe supply to the surface waters is also affected by upwelling of sub-surface waters in the coastal region of the Arabian Sea during the SW Monsoon. Despite the proximity of high concentrations of Fe in the shallow sub-oxic layer, freshly upwelled water is not drawn from this layer and the NO3/Fe ratio in the initially upwelled water is below the value at which Fe limitation is through to occur. Continued deposition of eolian Fe into the upwelled water as it advects offshore provides the Fe required to raise this ratio above the Fe limitation value.  相似文献   

18.
In the Eastern North Atlantic Ocean iron (Fe) speciation was investigated in three size fractions: the dissolvable from unfiltered samples, the dissolved fraction (<0.2 μm) and the fraction smaller than 1000 kDa (<1000 kDa). Fe concentrations were measured by flow injection analysis and the organic Fe complexation by voltammetry. In the research area the water column consisted of North Atlantic Central Water (NACW), below which Mediterranean Overflow Water (MOW) was found with the core between 800 and 1000 m depth. Below 2000 m depth the North Atlantic Deep Water (NADW) proper was recognised. Dissolved Fe and Fe in the <1000 kDa fraction showed a nutrient like profile, depleted at the surface, increasing until 500–1000 m depth below which the concentration remained constant. Fe in unfiltered samples clearly showed the MOW with high concentrations (4 nM) compared to the overlying NACW and the underlying NADW, with 0.9 nM and 2 nM Fe, respectively. By using excess ligand (Excess L) concentrations as parameter we show a potential to bind Fe. The surface mixed layer had the highest excess ligand concentrations in all size fractions due to phytoplankton uptake and possible ligand production. The ratio of Excess L over Fe proved to be a complementary tool in revealing the relative saturation state of the ligands with Fe. In the whole water column, the organic ligands in the larger colloidal fraction (between 0.2 μm and 1000 kDa) were saturated with Fe, whereas those in the smallest fraction (<1000 kDa) were not saturated with Fe, confirming that this fraction was the most reactive one and regulates dissolution and colloid aggregation and scavenging processes. This regulation was remarkably stable with depth since the alpha factor (product of Excess L and K′), expressing the reactivity of the ligands, did not vary and was 1013. Whereas, in the NACW and the MOW, the ligands in the particulate (>0.2 μm) fraction were unsaturated with Fe with respect to the dissolved fraction, thus these waters had a scavenging potential.  相似文献   

19.
The concentration level of cadmium (Cd) and the regeneration related to phosphate (PO4) were examined at two stations (CM10, CM12) in the eastern Japan Basin in July 1998. The observed Cd concentrations were around 0.2–0.3 nM and 0.5–0.6 nM in the surface and deep layers (Japan Sea Proper Water; JSPW), respectively; the concentration of Cd in the JSPW was much lower than that in the Pacific deep water, which is attributed to its specific formation system (which driven by the winter convection of the surface layer within the Japan Sea, thereafter descending to the deep layer) connected with the relatively active vertical mixing in the Japan Sea. A plot of Cd against PO4 showed good linearity with positive y-intercept values, suggesting that the excess Cd was apparently not available in the biogeochemical cycle. The molecular ratios of consumed O2 to regenerated Cd and PO4 in the JSPW were 688,000, 140 and 881,000, 146 for CM10 and CM12, respectively, and a lower preformed Cd concentration (around 0.37 nM) was also estimated in the JSPW, different from that of the North Pacific deep water (613,000 for Cd, 170 for PO4, and 0.64 nM of preformed Cd).  相似文献   

20.
Aerosol (soluble and total) iron and water-column dissolved (DFe, < 0.2 μm) and total dissolvable (TDFe, unfiltered) iron concentrations were determined in the Canary Basin and along a transect towards the Strait of Gibraltar, in order to sample across the Saharan dust plume. Cumulative dust deposition fluxes estimated from direct aerosol sampling during our one-month cruise are representative of the estimated deposition fluxes based on near surface water dissolved aluminium concentrations measured on board. Iron inventories in near surface waters combined with flux estimates confirmed the relatively short residence time of DFe in waters influenced by the Saharan dust plume (6–14 months). Enhanced near surface water concentrations of DFe (5.90–6.99 nM) were observed at the Strait of Gibraltar mainly due to inputs from metal-rich rivers. In the Canary Basin and the transect towards Gibraltar, DFe concentrations (0.07–0.76 nM) were typical of concentrations observed in the surface North Atlantic Waters, with the highest concentrations associated with higher atmospheric inputs in the Canary Basin. Depth profiles showed that DFe and TDFe were influenced by atmospheric inputs in this area with an accumulation of aeolian Fe in the surface waters. The sub-surface minimum of both DFe and TDFe suggests that a simple partitioning between dissolved and particulate Fe is not obvious there and that export may occur for both phases. At depths of around 1000–1300 m, both regeneration and Meddies may explain the observed maximum. Our data suggest that, in deep waters, higher particle concentrations likely due to dust storms may increase the scavenging flux and thus decrease DFe concentrations in deep waters.  相似文献   

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