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1.
Between 1988 and 1994, twenty time-series sediment traps were deployed at different water depths in the Canary Island region, off Cape Blanc (Mauritania), and off Cape Verde (Senegal). Lithogenic particle fluxes and grain size distributions of the carbonate-free fraction of the trapped material show a high impact of dust transported either in the northeast trade winds or the Saharan Air Layer (SAL). Highest annual mean lithogenic fluxes (31.2–56.1 mg m-2 d-1) were observed at the Cape Blanc site, and largest annual mean diameters (>6 μm) were found off Cape Verde (14.5–16.9 μm) and off Cape Blanc (15.2–16.7 μm). Lowest annual lithogenic fluxes (11.4–21.2 mg m-2 d-1 ) and smallest mean diameters (13.5–13.7 μm) occurred in the Canary Island region. A significant correlation of organic carbon and lithogenic fluxes was observed at all sites. Off Cape Blanc, fluxes and mean diameters correlated well between upper (around 1000 m depth) and lower traps (around 3500 m depth), indicating a fast and mostly undisturbed downward transport of particulate matter. In contrast, a major correlation of fluxes without correlating mean diameters occurred in the Canary Island region, which translates into a fast vertical transport plus scavenging of laterally advected material with depth at this site. The seasonality of lithogenic fluxes was highest in the Canary Island region and off Cape Verde, reflecting strong seasonal patterns of atmospheric circulation, with highest occurrence of continental winds in the trade wind layer during winter. In addition, grain size statistics reflect a dominant change of dust transport in the trade winds during winter/spring and transport in the SAL during summer 1993 at the Cape Verde site. Highest lithogenic fluxes during winter were correlated with mean diameters around 10–13 μm, whereas lower fluxes during summer consisted of coarse grains around 20 μm. Annual mean dust input wascalculated from lithogenic fluxes in the range 0.7×106–1.4×106 t yr-1, roughly confirming both sediment accumulation rates and atmospheric model calculations reported previously from this area.  相似文献   

2.
Investigations of lithogenic and biogenic particle fluxes using long-term sediment traps are still very rare in the northern high latitudes and are restricted to the arctic marginal seas and sub-arctic regions. Here data on the variability of fluxes of lithogenic matter, CaCO3, opal, and organic carbon and biomarker composition from the central Arctic Ocean are presented for a 1-year period. The study was carried out on material obtained from a long-term mooring system equipped with two multi-sampling traps, at 150 and 1550 m depth, and deployed on the southern Lomonosov Ridge close to the Laptev Sea continental margin from September 1995 to August 1996. In addition, data from surface sediments were included in the study. Annual fluxes of lithogenic matter, CaCO3, opal, and particulate organic carbon were 3.9, 0.8, 2.6, and 1.5 g m−2 y−1, respectively, in the shallow trap and 11.3, 0.5, 2.9, and 1.05 g m−2 y−1, respectively, in the deep trap.Both the shallow and the deep trap showed significant variations in vertical flux over the year. Higher values were found from mid-July to the end of October (total mass flux of 75–130 mg m−2 d−1 in the shallow trap and 40–225 mg m−2 d−1 in the deep trap). During all other months, fluxes were fairly low in both traps (most total mass flux values <10 mg m−2 d−1). The interval of increased fluxes can be separated into (1) a mid-July/August maximum caused by increased primary production as documented in high abundances of marine biomarkers and diatoms and (2) a September/October maximum caused by increased influence of Lena River discharge indicated by maximum lithogenic flux and large amounts of terrigenous/fluvial biomarkers in both traps. During September/October, total mass fluxes in the deep trap were significantly higher than in the shallow trap, suggesting a lateral sediment flux at greater depth. The lithogenic flux data also support the importance of sediment input from the Laptev Sea for the sediment accumulation on the Lomonosov Ridge on geological time scales, as indicated in sedimentary records from this region.  相似文献   

3.
The total organic carbon (TOC) and total inorganic carbon (CT) exchange between the Atlantic Ocean and the Mediterranean Sea was studied in the Strait of Gibraltar in September 1997. Samples were taken at eight stations from western and eastern entrances of the Strait and at the middle of the Strait (Tarifa Narrows). TOC was analyzed by a high-temperature catalytic oxidation method, and CT was calculated from alkalinity–pHT pairs and appropriate thermodynamic relationships. The results are used in a two-layer model of water mass exchange through the Strait, which includes the Atlantic inflow, the Mediterranean outflow and the interface layer in between. Our observations show a decrease of TOC and an increase of CT concentrations from the surface to the bottom: 71–132 μM C and 2068–2150 μmol kg−1 in the Surface Atlantic Water, 74–95 μM C and 2119–2148 μmol kg−1 in the North Atlantic Central Water, 63–116 μM C and 2123–2312 μmol kg−1 in the interface layer, and 61–78 μM C and 2307–2325 μmol kg−1 in the Mediterranean waters. However, within the Mediterranean outflow, we found that the concentrations of carbon were higher at the western side of the Strait (75–78 μM C, 2068–2318 μmol kg−1) than at the eastern side (61–69 μM C, 2082–2324 μmol kg−1). This difference is due to the mixing between the Atlantic inflow and the Mediterranean outflow on the west of the Strait, which results in a flux of organic carbon from the inflow to the outflow and an opposite flux of inorganic carbon. We estimate that the TOC input from the Atlantic Ocean to the Mediterranean Sea through the Strait of Gibraltar varies from (0.97±0.8)104 to (1.81±0.90)104 mol C s−1 (0.3×1012 to 0.56×1012 mol C yr−1), while outflow of inorganic carbon ranges from (12.5±0.4)104 to (15.6±0.4)104 mol C s−1 (3.99–4.90×1012 mol C yr−1). The high variability of carbon exchange within the Strait is due to the variability of vertical mixing between inflow and outflow along the Strait. The prevalence of organic carbon inflow and inorganic carbon outflow shows the Mediterranean Sea to be a basin of active remineralization of organic material.  相似文献   

4.
The first carbon budget constructed for the Barents Sea to study the fluxes of carbon into, out of, and within the region is presented. The budget is based on modelled volume flows, measured dissolved inorganic carbon (DIC) concentration, and literature values for dissolved organic carbon (DOC) and particulate organic carbon (POC) concentrations. The results of the budget show that ～5600±660×106 t C yr?1 is exchanged through the boundaries of the Barents Sea. If a 40% uncertainty in the volume flows is included in the error calculation it resulted in a total uncertainty of ±1600×106 t C yr?1. The largest part of the total budget flux consists of DIC advection (～95% of the inflow and ～97% of the outflow). The other sources and sinks are, in order of importance, advection of organic carbon (DOC+POC; ～3% of both in- and outflow), total uptake of atmospheric CO2 (～1% of the inflow), river and land sources (～0.2% of the inflow), and burial of organic carbon in the sediments (～0.2% of the outflow). The Barents Sea is a net exporter of carbon to the Arctic Ocean; the net DIC export is ～2500±660×106 t C yr?1 of which ～1700±650×106 t C yr?1 (～70%) is in subsurface water masses and thus sequestered from the atmosphere. The net total organic carbon export to the Arctic Ocean is ～80±20×106 t C yr?1. Shelf pumping in the Barents Sea results in an uptake of ～22±11×106 t C yr?1 from the atmosphere which is exported out of the area in the dense modified Atlantic Waters. The main part of this carbon was channelled through export production (～16±10×106 t C yr?1).  相似文献   

5.
Particulate fluxes of trace elements (Al, Cd, Co, Cu, Fe, Mn, Ni, P, Ti, V and Zn) in the northeast Atlantic Ocean (three positions at latitudes from 33°N to 54°N along ∼20°W) were measured using time-series sediment traps between March 1992 and September 1994. Significant variabilities of fluxes with season and depth (1000 m to maximum of 4000 m) were observed only for ‘biogenic elements’, such as Cd, Ni, Zn or P. On the other hand, we found a distinct large-scale increase of fluxes into the deep-sea traps to the south for Al, Co, Fe, Mn and V. We attribute this latitudinal gradient to the increasing influence of the Saharan dust plume. The biogenic flux decreased towards the south. This trend was clearly visible for Cd and P only. The fluxes of other ‘nutrient-like’ elements, such as Ni or Zn, exhibited a general decrease between 53°N and 33°N. We compared our sedimentation flux data with published data from the western North Atlantic basins. For this purpose we corrected the deep-sea fluxes of Cu, Mn, Ni and Zn for their lithogenic fractions on the basis of Al, with average crustal material and granitic rocks as references. The comparison indicates that these ‘excess’ fluxes are a factor of at least 2 higher in the western basins for the selected elements. Estimated fluxes are in good agreement with reported atmospheric deposition in the two areas. The noted imbalance between the non-lithogenic atmospheric input of Mn and the determined ‘excess flux’ in the deep northeast Atlantic indicates an additional input in the form of a lateral flux of dissolved Mn(II) species and scavenging onto sinking particles. With respect to the mechanism of sedimentation, a unique behaviour is noticed for the refractory elements Co, Fe, Mn, Ti and V, which were found to correlate with the vertical transport of Al (clay). The ‘excess’ fluxes of Cu, Ni and Zn are linearly related to Corg, whereas the overall relation of Cd to P fluxes exhibits a molar Cd/P ratio of 2.0×10-4, which is close to the ratio in the dissolved fractions in the northeast Atlantic.  相似文献   

6.
The lithogenic flux of sediment trap material was analyzed from a three year time series (February 2002–March 2005) at 2000 m depth in the Northeast Atlantic (Kiel 276, 33°N, 22°W) with regards to the seasonal and interannual variability of flux intensity and mineralogy—by applying an automated particle SEM-EDX analysis (scanning electron microscope-energy dispersive X-ray analysis). The lithogenic flux shows strong interannual variations with highest lithogenic flux rates occurring during January–February and April–March coupled to the total particle flux. Mean lithogenic flux rates for the sample years are 7.1 (2002–2003), 5.1 (2003–2004) and 16.1 mg m?2 d?1 (2004–2005). Mineral assemblages from the three sample years reveal distinct major minerals related to specific source regions. Clay minerals dominate the lithogenic fraction within the years 2002 and 2004 with illite (2002–2003) and palygorskite (2003–2004) being the major clay minerals. During the year 2004–2005, quartz is the major lithogenic mineral accompanied by smectite. The mineral assemblages hint to a mixture of North African source areas with dominant sources in Mauritania and north western parts of NW Africa for the years 2002–2004 and central Sahara (Algeria–Mali) within the year 2004–2005.  相似文献   

7.
North Atlantic sediment drifts are valuable archives for paleoceanographic reconstructions spanning various timescales. However, the short-term dynamics of such systems are poorly known, and this impinges on our ability to quantitatively reconstruct past change. Here we describe a high-resolution 319-day time-series of hydrodynamics and near-bottom (4 m) particulate matter flux variability at a 2600 m deep site with an extremely high sediment accumulation rate on the southern Gardar Drift in the North Atlantic. We compare our findings with the actual deposits at the site. The total annual particle flux amounted to ～360 g m?2 yr?1, varied from ～0.15 to >5.0 g m?2 day?1 and displayed strong seasonal compositional changes, with the highest proportion of fresh biogenic matter arriving after the spring bloom in June and July. Flux variability also depended on the changing input of lithogenic matter that had been (re)suspended for a longer time (decades). Active focussing of material from both sources is required to account for the composition and the magnitude of the total flux, which exceed observations elsewhere by an order of magnitude. The enhanced focussing or increased delivery appeared to be positively related to current velocity. The intercepted annual particle flux accounted for only 60% of the sediment accumulation rate of 600±20 g m?2 yr?1 (0.20±0.07 cm yr?1), indicating higher intra- and inter-annual variability of both the biogenic and lithogenic fluxes and/or advection of additional sediment closer to the seafloor (i.e. <4 m). This temporal variability in the composition and amount of material deposited highlights intra-annual changes in the flux of lithogenic material, but also underscores the importance of (reworked) sediment focussing and seasonality of the biogenic flux. All should be taken into account in the interpretation of the paleorecord from such depositional settings.  相似文献   

8.
Data from the first systematic survey of inorganic carbon parameters on a global scale, the GEOSECS program, are compared with those collected during WOCE/JGOFS to study the changes in carbon and other geochemical properties, and anthropogenic CO2 increase in the Atlantic Ocean from the 1970s to the early 1990s. This first data-based estimate of CO2 increase over this period was accomplished by adjusting the GEOSECS data set to be consistent with recent high-quality carbon data. Multiple Linear Regression (MLR) and extended Multiple Linear Regression (eMLR) analyses to these carbon data are applied by regressing DIC with potential temperature, salinity, AOU, silica, and PO4 in three latitudinal regions for the western and eastern basins in the Atlantic Ocean. The results from MLR (and eMLR provided in parentheses) indicate that the mean anthropogenic CO2 uptake rate in the western basin is 0.70 (0.53) mol m?2 yr?1 for the region north of 15°N; 0.53 (0.36) mol m?2 yr?1 for the equatorial region between 15°N and 15°S; and 0.83 (0.35) mol m?2 yr?1 in the South Atlantic south of 15°S. For the eastern basin an estimate of 0.57 (0.45) mol m?2 yr?1 is obtained for the equatorial region, and 0.28 (0.34) mol m?2 yr?1 for the South Atlantic south of 15°S. The results of using eMLR are systematically lower than those from MLR method in the western basin. The anthropogenic CO2 increase is also estimated in the upper thermocline from salinity normalized DIC after correction for AOU along the isopycnal surfaces. For these depths the results are consistent with the CO2 uptake rates derived from both MLR and eMLR methods.  相似文献   

9.
The distribution of transparent exopolymer particles (TEP) was investigated during a coccolithophorid bloom in the northern Bay of Biscay (North Atlantic Ocean) in early June 2006. MODIS chlorophyll-a (Chl-a) and reflectance images before and during the cruise were used to localize areas of important biological activity and high reflectance (HR). TEP profiles along the continental margin, determined using microscopic (TEPmicro) and colorimetric (TEPcolor) methods, showed abundant (6.1×106–4.4×107 L?1) and relatively small (0.5–20 μm) particles, leading to a low total volume fraction (0.05–2.2 ppm) of TEPmicro and similar vertical profiles of TEPcolor. Estimates of carbon content in TEP (TEP-C) derived from the microscopic approach yielded surface concentration of 1.50 μmol C L?1. The contribution of TEP-C to particulate organic carbon (POC) was estimated to be 12% (molar C ratio) during this survey. Our results suggest that TEP formation is a probable first step to rapid and efficient export of C during declining coccolithophorid blooms.  相似文献   

10.
An In Situ Ultraviolet Spectrophotometer (ISUS) was coupled to a benthic chamber to characterize the bisulfide flux emanating from a warm spring at the Extrovert Cliff locality within Monterey Bay, California. The chamber was periodically flushed with bottom seawater to reset chemical concentrations, which enabled deployments over multiple days. Data from several deployments, each lasting at least 10 days, were used to calculate flow rates, fluid concentrations, and fluxes over time. The bisulfide concentration of the fluid entering the chamber varied from 75 to 4500 μmol l?1. Positive temperature anomalies up to 3.5° were associated with these elevated concentrations. Linear flow rates ranged from 2 to >17 m day?1, while the bisulfide fluxes varied from 0.2 to 80 mol m?2 day?1. The bisulfide originated at depth and was not produced in the surface sediments via an anaerobic oxidation of methane coupled to sulfate reduction. Tides modulated the flow as well as the composition of the fluid entering the chamber. It appeared that a deep sourced fluid, which supplied the bisulfide, was mixed with a second, ambient seawater-like fluid before entering the flux chamber. At low tides, flow rates were at their highest and the contribution of the deep sourced fluid to the fluid entering the chamber was at a maximum.  相似文献   

11.
We observed the origin, behavior, and flux of dissolved organic carbon (DOC), dissolved organic nitrogen (DON), colored dissolved organic matter (CDOM), and dissolved inorganic nitrogen (DIN) in the subterranean estuary of a volcanic island, Jeju, Korea. The sampling of surface seawater and coastal groundwater was conducted in Hwasun Bay, Jeju, in three sampling campaigns (October 2010, January 2011, and June 2011). We observed conservative mixing of these components in this subterranean environment for a salinity range from 0 to 32. The fresh groundwater was characterized by relatively high DON, DIN, and CDOM, while the marine groundwater showed relatively high DOC. The DON and DIN fluxes through submarine groundwater discharge (SGD) in the groundwater of Hwasun Bay were estimated to be 1.3 × 105 and 2.9 × 105 mol d− 1, respectively. In the seawater of Hwasun Bay, the groundwater-origin DON was almost conservative while about 91% of the groundwater-origin DIN was removed perhaps due to biological production. The DON flux from the entire Jeju was estimated to be 7.9 × 108 mol yr− 1, which is comparable to some of the world's large rivers. Thus, our study highlights that DON flux through SGD is potentially important for delivery of organic nitrogen to further offshore while DIN is readily utilized by marine plankton in near-shore waters under N-limited conditions.  相似文献   

12.
A study of organic carbon mineralization from the Congo continental shelf to the abyssal plain through the Congo submarine channel and Angola Margin was undertaken using in situ measurements of sediment oxygen demand as a tracer of benthic carbon recycling. Two measurement techniques were coupled on a single autonomous platform: in situ benthic chambers and microelectrodes, which provided total and diffusive oxygen uptake as well as oxygen microdistributions in porewaters. In addition, sediment trap fluxes, sediment composition (Org-C, Tot-N, CaCO3, porosity) and radionuclide profiles provided measurements of, respectively input fluxes and burial rate of organic and inorganic compounds.The in situ results show that the oxygen consumption on this margin close to the Congo River is high with values of total oxygen uptake (TOU) of 4±0.6, 3.6±0.5 mmol m−2 d−1 at 1300 and 3100 m depth, respectively, and between 1.9±0.3 and 2.4±0.2 mmol m−2 d−1 at 4000 m depth. Diffusive oxygen uptakes (DOU) were 2.8±1.1, 2.3±0.8, 0.8±0.3 and 1.2±0.1 mmol m−2 d−1, respectively at the same depths. The magnitude of the oxygen demands on the slope is correlated with water depth but is not correlated with the proximity of the submarine channel–levee system, which indicates that cross-slope transport processes are active over the entire margin. Comparison of the vertical flux of organic carbon with its mineralization and burial reveal that this lateral input is very important since the sum of recycling and burial in the sediments is 5–8 times larger than the vertical flux recorded in traps.Transfer of material from the Congo River occurs through turbidity currents channelled in the Congo valley, which are subsequently deposited in the Lobe zone in the Congo fan below 4800 m. Ship board measurements of oxygen profiles indicate large mineralization rates of organic carbon in this zone, which agrees with the high organic carbon content (3%) and the large sedimentation rate (19 mm y−1) found on this site. The Lobe region could receive as high as 19 mol C m−2 y−1, 1/3 being mineralized and 2/3 being buried and could constitute the largest depocenter of organic carbon in the South Atlantic.  相似文献   

13.
The Lophelia pertusa community at Viosca Knoll (VK826) is the most extensive found to date in the Gulf of Mexico. As part of a multi-disciplinary study, the physical setting of this area was described using benthic landers, CTD transects and remotely operated vehicle observations. The site was broadly characterised into three main habitats: (1) dense coral cover that resembles biogenic reef complexes, (2) areas of sediment, and (3) authigenic carbonate blocks with sparse coral and chemosynthetic communities. The coral communities were dominated by L. pertusa but also contained numerous solitary coral species. Over areas that contained L. pertusa, the environmental conditions recorded were similar to those associated with communities in the north-eastern Atlantic, with temperature (8.5–10.6 °C) and salinity (～35) falling within the known species niche for L. pertusa. However, dissolved oxygen concentrations (2.7–2.8 ml l?1) and density (σΘ, 27.1–27.2 kg m?3) were lower and mass fluxes from sediment trap data appeared much higher (4002–4192 mg m?2 d?1). Yet, this species still appears to thrive in this region, suggesting that L. pertusa may not be as limited by lower dissolved oxygen concentrations as previously thought. The VK826 site experienced sustained eastward water flow of 10–30 cm s?1 over the 5-day measurement period but was also subjected to significant short-term variability in current velocity and direction. In addition, two processes were observed that caused variability in salinity and temperature; the first was consistent with internal waves that caused temperature variations of 0.8 °C over 5–11 h periods. The second was high-frequency variability (20–30 min periods) in temperature recorded only at the ALBEX site. A further pattern observed over the coral habitat was the presence of a 24 h diel vertical migration of zooplankton that may form part of a food chain that eventually reaches the corals. The majority of detailed studies concerning local environmental conditions in L. pertusa habitats have been conducted within the north-eastern Atlantic, limiting most knowledge of the niche of this species to a single part of an ocean basin. Data presented here show that the corals at VK826 are subjected to similar conditions in temperature, salinity, and flow velocity as their counterparts in the north-east Atlantic, although values for dissolved oxygen and density (sigma-theta: σΘ) are different. Our data also highlight novel observations of short-term environmental variability in cold-water coral habitat.  相似文献   

14.
The Amazon River Plume delivers freshwater and nutrients to an otherwise oligotrophic western tropical North Atlantic (WTNA) Ocean. Plume waters create conditions favorable for carbon and nitrogen fixation, and blooms of diatoms and their diazotrophic cyanobacterial symbionts have been credited with significant CO2 uptake from the atmosphere. The fate of the carbon, however, has been measured previously by just a few moored or drifting sediment traps, allowing only speculation about the full extent of the plume's impact on carbon flux to the deep sea. Here, we used surface (0.5 m) sediment cores collected throughout the Demerara Slope and Abyssal Plain, at depths ranging from 1800 to 5000 m, to document benthic diagenetic processes indicative of carbon flux. Pore waters were extracted from sediments using both mm- and cm-scale extraction techniques. Profiles of nitrate (NO3) and silicate (Si(OH)4) were modeled with a diffusion-reaction equation to determine particulate organic carbon (POC) degradation and biogenic silica (bSi) remineralization rates. Model output was used to determine the spatial patterns of POC and bSi arrival at the sea floor. Our estimates of POC and Si remineralization fluxes ranged from 0.16 to 1.92 and 0.14 to 1.35 mmol m−2 d−1, respectively. A distinct axis of POC and bSi deposition on the deep sea floor aligned with the NW axis of the plume during peak springtime flood. POC flux showed a gradient along this axis with highest fluxes closest to the river mouth. bSi had a more diffuse zone of deposition and remineralization. The impact of the Amazon plume on benthic fluxes can be detected northward to 10°N and eastward to 47°W, indicating a footprint of nearly 1 million km2. We estimate that 0.15 Tmol C y−1 is remineralized in abyssal sediments underlying waters influenced by the Amazon River. This constitutes a relatively high fraction (~7%) of the estimated C export from the region.; the plume thus has a demonstrable impact on Corg export in the western Atlantic. Benthic fluxes under the plume were comparable to and in some cases greater than those observed in the eastern equatorial Atlantic, the southeastern Atlantic, and the Southern Ocean.  相似文献   

15.
Previous work has shown that methane anomalies frequently occur within the rift valley of the Mid-Atlantic Ridge (MAR). The plumes appear confined within the high, steep walls of the valley, and it is not known whether methane may escape to the open ocean outside. In order to investigate this question, the concentration and 13C/12C ratio of methane together with CCl3F concentration were measured in the northeastern Atlantic including the rift valley near 50°N. This segment contained methane plumes centered several 100 m above the valley floor with δ13C values mostly between –15‰ and –10‰. A limited number of helium isotope measurements showed that δ3He increased to 17% at the bottom of the valley, which suggests the helium and methane sources may be spatially separated. In the eastern Atlantic away from the ridge (48°N, 20°W), the methane concentration decreased monotonically from the surface to the bottom, but the methane δ13C exhibited a mid-water maximum of about –25‰. The bottom water methane contained a significantly lower δ13C of about –36‰. Thus, it appears that isotopically heavy methane escapes from the MAR into North Atlantic Deep Water (NADW) that contacts the ridge crest while circulating to the east. The formation of NADW supplies isotopically light methane that dilutes the input of heavy carbon from the ridge. We employed a time-dependent box model to calculate the extent of isotope dilution and thereby the flux of MAR methane into the NADW circulation. The degree of methane oxidation, which affects the 13C/12C of methane through kinetic isotope fractionation, was estimated by comparing methane and CFC-11 model results with observations. The model calculations indicate a MAR methane source of about 0.06×10−9 mol L−1 yr−1 to waters at the depth of the ridge crest. Assuming this extends to a 500 m thick layer over half of the entire Atlantic, the amount of methane escaping from the MAR to the open ocean is estimated to be about 1×109 mol yr−1. The total production of methane within the rift valley is likely much greater than the flux from the valley to the outside because of local oxidation. This implies that serpentinization of ultramafic rocks supports much of methane production in the rift valley because the amount expected from basalt degassing in association with mantle helium (<0.6×109 mol CH4 yr−1) is less than even the net amount escaping from the valley. The model results also indicate the methane specific oxidation rate is about 0.05 yr−1 in open waters of the northern Atlantic.  相似文献   

16.
Since 2000 long-term measurements of vertical particle flux have been performed with moored sediment traps at the long-term observatory HAUSGARTEN in the eastern Fram Strait (79°N/4°E). The study area, which is seasonally covered with ice, is located in the confluence zone of the northward flowing warm saline Atlantic water with cold, low salinity water masses of Arctic origin. Current projections suggest that this area is particularly vulnerable to global warming. Total matter fluxes and components thereof (carbonate, particulate organic carbon and nitrogen, biogenic silica, biomarkers) revealed a bimodal seasonal pattern showing elevated sedimentation rates during May/June and August/September. Annual total matter flux (dry weight, DW) at ～300 m depth varied between 13 and 32 g m?2 a?1 during 2000 and 2005. Of this total flux 6–13% was due to CaCO3, 4–21% to refractory particulate organic carbon (POC), and 3–8% to biogenic particulate silica (bPSi). The annual flux of all biogenic components together was almost constant during the period studied (8.5–8.8 g m?2 a?1), although this varied from 27% to 67% of the total annual flux. The fraction was lowest in a year characterized by the longest duration of ice coverage (91 and 70 days for the calendar year and summer season, May–September, respectively). Biomarker analyses revealed that organic matter originating from marine sources was present in excess of terrigenious material in the sedimented matter throughout most of the study period. Fluxes of recognizable phyto- and protozooplankton cells amounted up to 60×106 m?2 d?1. Diatoms and coccolithophorids were the most abundant organisms. Diatoms, mainly pennate species, dominated during the first years of the investigation. A shift in the composition occurred during the last year when numbers of diatoms declined considerably, leading to a dominance of coccolithoporids. This was also reflected in a decrease in the sedimentation of bPSi. The sedimentation of biogenic matter, however, did not differ from the amount observed during the previous years. Among the larger organisms, pteropods at times contributed significantly to both the total matter and CaCO3, fluxes.  相似文献   

17.
The vertical sinking flux of particulate Al, Fe, Pb, and Ba from the upper 250 m of the Labrador Sea has been estimated from measurements of 234Th/238U disequilibrium and the respective metal/234Th ratios in >53 μm size particles. 234Th-derived particulate metal fluxes include in situ scavenged metals, labile lithogenic metals, and metals derived from external input (e.g., atmospheric supply). In contrast to the POC/234Th ratio, particle size-fractionated (0.4–10 μm, 10–53 μm, and >53 μm) Al/234Th, Fe/234Th and Pb/234Th, and Ba/234Th ratios generally increase with depth and exhibit no systematic change with particle diameter. Sinking fluxes of particulate Al (2.47–22.3 μmol m−2 d−1), Fe (2.69–16.3 μmol m−2 d−1), Pb (2.85–70 nmol m−2 d−1), and Ba (0.13–2.1 μmol m−2 d−1) at 50 m (base of the euphotic zone) and 100 m (base of the mixed layer) are largely within the range of previous sediment trap results from other ocean basins. Estimates of the upper ocean residence time of Al (0.07–0.28 yr) and Pb (0.8–2.9 yr) are short compared to previously reported values. The settling rate of >53 μm particles calculated from the 234Th data ranges from 14 to 38 m d−1.  相似文献   

18.
Coccoliths collected by sediment traps deployed on the slope of the Bay of Biscay (northeastern Atlantic), from June 1990 to August 1991, were examined to determine their contribution to the transport of carbonate on a mid-latitude continental margin. They also were used as tracers of particle transfer processes on this slope. Two traps located at 1900 m, respectively at 2300 (Mooring Site 1) and 3000 m (Mooring Site 2) water depths provided high-resolution (4–7 days) time-series samples covering a 14-month period at MS2 and a 3-month period at MS1. Coccoliths from 28 species were identified over the course of the experiment, among which Emiliania huxleyi was always dominant (relative abundance range: 59–93%). Total coccoliths number fluxes were high but variable, ranging from 390×106 to 1610×106 coccoliths m−2 day−1 at MS1, and from 58×106 to 1500×106 coccoliths m−2 day−1 at MS2. The time-weighted mean flux, calculated for the whole experiment at MS2, was 499×106 coccoliths m−2 day−1. Estimate of coccoliths minimal contribution to total carbonate flux at 1900 m depth averaged 12%, which represented a weighted mean flux of 7.3 mg m−2 day−1 (2.7 g m−2 yr−1). Lateral transport of coccoliths resuspended from shelf and/or upper slope sediments seems to be the dominant transfer process to depth on this northeastern Atlantic slope. Nevertheless, the clear seasonal succession observed in the species composition implies that the deposition/resuspension/transport sequence is rapid (presumably less than a few months). Several short and unsmoothed signals directly issued from coccoliths bloom events also were recorded in our traps, a result that indicates rapid settling rates. The overall coccolith sedimentation processes appear as being quite diversified, but quantitative and qualitative analyses of aggregates collected by the traps suggest that they are important carriers of coccoliths in this margin environment.  相似文献   

19.
Measurements of particle size-fractionated POC/234Th ratios and 234Th and POC fluxes were conducted using surface-tethered, free-floating, sediment traps and large-volume in-situ pumps during four cruises in 2004 and 2005 to the oligotrophic eastern Mediterranean Sea and the seasonally productive western Mediterranean and northwest Atlantic. Analysis of POC/234Th ratios in sediment trap material and 10, 20, 53, 70, and 100 μm size-fractionated particles indicate, for most stations, decreasing ratios with depth, a weak dependence on particle size, and ratios that converge to ～1–5 μmol dpm?1 below the euphotic zone (～100–150 m) throughout the contrasting biogeochemical regimes. In the oligotrophic waters of the Aegean Sea, 234Th and POC fluxes estimated using sediment traps were consistently higher than respective fluxes estimated from water-column 234Th–238U disequilibrium, observations that are attributed to terrigenous particle scavenging of 234Th. In the more productive western Mediterranean and northwest Atlantic, 234Th and POC fluxes measured by sediment trap and 234Th–238U disequilibrium agreed within a factor of 2–4 throughout the water column. An implication of these results is that estimates of POC export by sediment traps and 234Th–238U disequilibrium can be biased differently because of differential settling speeds of POC and 234Th-carrying particles.  相似文献   

20.
Fixed nitrogen is a key nutrient involved in regulating global marine productivity and hence the global oceanic carbon cycle. Oceanic nitrogen (N2) fixation is estimated to supply 8×1012 moles N y?1 to the ocean, approximately equal to current riverine and the atmospheric inputs of fixed N, and between 50 and 100% of current estimates of oceanic denitrification. However, the spatial and temporal variability of N2 fixation remains uncertain, mostly because of the normal low resolution sampling for diazotroph distribution and fixation rates. It is well established that N2 fixation, mediated by the enzyme nitrogenase, is a source of hydrogen (H2), but the extent to which it leads to supersaturation of H2 in oceanic waters is unresolved. Here, we present simultaneous measurements of upper ocean dissolved H2 concentration (nmol L?1), and rates of N2 fixation (μmol N m?3 d?1), determined using 15N2 tracer techniques (at 7 or 15 m), on a transect from Fiji to Hawaii. We find a significant correlation (r=0.98) between dissolved H2 and rates of N2 fixation, with the greatest supersaturation of H2 and highest rates of N2 fixation being observed in the subtropical gyres at the southern (～18°S) and northern (18°N) reaches of the transect. The lowest H2 saturation and N2 fixation were observed in the equatorial region between 8°S and 14°N. We propose that an empirical relationship between H2 supersaturations and N2 fixation measurements could be used to guide sampling for 15N fixation measurements or to aid the spatial interpolation of such measurements.  相似文献   

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