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1.
An extended time series of particle fluxes at 3800 m was recorded using automated sediment traps moored at Ocean Station Papa (OSP, 50°N, 145°W) in the northeast Pacific Ocean for more than a decade (1982–1993). Time-series observations at 200 and 1000 m, and short-term measurements using surface-tethered free-drifting sediment traps also were made intermittently. We present data for fluxes of total mass (dry weight), particulate organic carbon (POC), particulate organic nitrogen (PON), biogenic Si (BSi), and particulate inorganic carbon (PIC) in calcium carbonate. Mean monthly fluxes at 3800 m showed distinct seasonality with an annual minimum during winter months (December–March), and maximum during summer and fall (April–November). Fluxes of total mass, POC, PIC and BSi showed 4-, 10-, 7- and 5-fold increases between extreme months, respectively. Mean monthly fluxes of PIC often showed two plateaus, one in May–August dominated by <63 μm particles and one in October–November, which was mainly >63 μm particles. Dominant components of the mass flux throughout the year were CaCO3 and opal in equal amounts. The mean annual fluxes at 3800 m were 32±9 g dry weight g m−2 yr−1, 1.1±0.5 g POC m−2 yr−1, 0.15±0.07 g PON m−2 yr−1, 5.9±2.0 g BSi m−2 yr−1 and 1.7±0.6 g PIC m−2 yr−1. These biogenic fluxes clearly decreased with depth, and increased during “warm” years (1983 and 1987) of the El Niño, Southern Oscillation cycle (ENSO). Enhancement of annual mass flux rates to 3800 m was 49% in 1983 and 36% in 1987 above the decadal average, and was especially rich in biogenic Si. Biological events allowed estimates of sinking rates of detritus that range from 175 to 300 m d−1, and demonstrate that, during periods of high productivity, particles sink quickly to deep ocean with less loss of organic components. Average POC flux into the deep ocean approximated the “canonical” 1% of the surface primary production.  相似文献   

2.
With the aim of improving the knowledge of the open ocean carbon cycle, we present a budget of particulate organic carbon (POC) fluxes carried out in the deep central part of the Algero-Balearic Basin (ABB) at 2850 m water depth based on a single mooring equipped with five automated sediment traps deployed from April 2001 to May 2002 at depths of 250, 845, 1440, 2145 and 2820 m. Suspended particulate matter (SPM) and superficial sediments were also used as indicators of hydrodynamics and carbon burial, respectively. The data reveal that the fraction of primary production buried in the sediment, which finally leads to the sequestration of carbon dioxide from the atmosphere, is 0.16%, lower than the values found in the nearby continental margin regions such as the Alboran Sea (0.48–0.89%) but of the same order as recorded at other Mediterranean sites at similar depths, such as the Ionian Sea (0.11%). As they sink through the water column, the particles exhibit decreases in flux that are similar to those observed elsewhere, but also show variations that appear to correlate with hydrological features of the water masses present in the basin, as revealed by SPM concentrations and compositions. The input of the tyrrhenian deep water (TDW) into the ABB at 800–1500 m of water depth exhibits low suspended POC concentrations and low sinking POC fluxes were also observed in this depth range. Gulf of Lions water mass formation appears to also contribute to elevated suspended POC concentrations and perhaps POC accumulation in the traps and sediments by spreading of dense cold water along the whole ABB that supplied POC at depths higher than 2000 m.  相似文献   

3.
Time-series measurements of 234Th activities and particulate organic carbon (POC) concentrations were made at time-series stations (K1, K2, K3, and KNOT) in the northwestern North Pacific from October 2002 to August 2004. Seasonal changes in POC export fluxes from the surface layer (∼100 m) were estimated using 234Th as a tracer. POC fluxes varied seasonally from approximately 0 to 180 mg C m−2 d−1 and were higher in spring–summer than in autumn–winter. The export ratio (e-ratio) ranged from 6% to 55% and was also higher in spring–summer. Annual POC fluxes were estimated to be 31 g C m−2 y−1 in the subarctic region (station K2) and 23 g C m−2 y−1 in the region between the subarctic and subtropical gyres (station K3). POC fluxes and e-ratios in the northwestern North Pacific were much higher than those in most other oceans. The annual POC flux corresponded to 69% of annual new production estimated from the seasonal difference of the nutrient in the Western Subarctic Gyre (45 g C m−2 y−1). These results indicate that much of the organic carbon assimilated in the surface layer of the northwestern North Pacific is transferred to the deep ocean in particulate form. Our conclusions support previous reports that diatoms play an important role in the biological pump.  相似文献   

4.
The relationship between particulate organic carbon (POC) concentrations measured in modern sediment and fluxes of exported POC to the sediment surface needs to be understood in order to use POC content as a proxy of paleo-environmental conditions. The objective of our study was to compare POC concentrations, POC mineralization rates calculated from O2 consumption and POC burial rates. Benthic O2 distributions were determined in 58 fine-grained sediment cores collected at different periods at 14 stations in the southeastern part of the Bay of Biscay with depths ranging from 140 to 2800 m. Depth-dependent volume-specific oxygen consumption rates were used to assess rates of aerobic oxidation of organic matter (OM), assuming that O2 consumption solely was related to heterotrophic activity at the sediment–water interface. Heterogeneity of benthic O2 fluxes denoted changes in time and space of fresh organic material sedimentation. The most labile fraction of exported POC engendered a steep decrease in concentration in the upper 5 mm of vertical O2 profiles. The rupture in the gradient of O2 microprofile may be related to the bioturbation-induced mixing depth of fast-decaying carbon. Average diffusive O2 fluxes showed that this fast-decaying OM flux was much higher than buried POC, although diffusive O2 fluxes underestimated the total sediment oxygen demand, and thus the fast-decaying OM flux to the sediment surface. Sedimentary POC burial was calculated from sediment mass accumulation rate and the organic carbon content measured at the top of the sediment. The proportion of buried POC relative to total exported POC ranged at the most between 50% and 10%, depending on station location. Therefore, for a narrow geographic area like the Bay of Biscay, burial efficiency of POC was variable. A fraction of buried POC consisted of slow-decaying OM that was mineralized within the upper decimetres of sediment through oxic and anoxic processes. This fraction was deduced from the decrease with depth in POC concentration. At sites located below 500 m water depth, where the fast-decaying carbon did not reach the anoxic sediment, the slow-decaying pool may control the O2 penetration depth. Only refractory organic material was fossilized in sedimentary records at locations where labile OM did not reach the anoxic portion of the sediment.  相似文献   

5.
Surface concentrations and vertical fluxes of particulate organic carbon (POC) were assessed in the Amundsen Gulf (southeastern Beaufort Sea, Arctic Ocean) over the years 2004 to 2006 by using ocean color remote-sensing imagery and sequential sediment traps moored over the ca. 400 m isobath. Environmental conditions (sea ice, wind) and oceanographic variables (temperature, salinity, fluorescence and currents) were investigated to explain the variability of POC data. Annual downward POC fluxes in 2004, 2005 and 2006 cumulated, respectively, to 3.3, 4.2 and 6.0 g C m?2 yr?1 at ～100 m depth, and to 1.3, 2.2 and 3.3 g C m?2 yr?1 at ～210 m depth. The fraction of settling POC attributable to autochthonous processes occurring at or next to ice break-up was estimated to be 75–84% of the 100 m annual fluxes and to be 61–75% of the 210 m fluxes. Over the three ice-reduced seasons, distinct scenarios between ice conditions, surface POC pools and vertical POC export at 100 m were identified: (1) in 2004, despite a normal ice break-up, a weak primary production was measured and low vertical fluxes were collected as old ice moved across the region; (2) in 2005, a lengthened ice-free period allowed an extended season of surface POC production near-shore, while an intermediate increase of vertical fluxes was recorded offshore; and (3) in 2006, a late ice melt gave rise to a pulsed ice edge bloom and to large vertical fluxes also associated with extra ice-flushed material. Linear regressions of vertical POC fluxes against satellite-derived surface POC concentrations suggested that the pelagic POC retention in the upper 100 m of the Amundsen Gulf ranged from ca. 70% to 90% depending on the timing of ice cover melt. Regardless of the inter-annual variability, the estimated fraction of the surface POC reservoir reaching the 210 m water depth was reduced to ～5%. Therefore, as the Arctic Ocean warms up, our results support the expectation that the increasing extent of the seasonal ice zone will promote the POC pathways that benefit pelagic webs rather than benthic communities.  相似文献   

6.
In this study at the Bermuda Atlantic Time-series Study (BATS) site we demonstrate that the polonium–lead disequilibrium system may perform better as a tracer of organic carbon export under low-flux conditions (in this case, <2.5 mmol C m?2 d?1) than under bloom conditions in an oligotrophic setting. With very few exceptions, the POC flux predictions calculated from the water-column 210Po deficit were within a factor of 2 of the POC flux caught in surface-tethered sediment traps. However, we found higher correlation between size-fractionated particulate 210Po activity and POC concentration in November 2006 (r=0.93) than in January (r=0.79) and during the spring bloom in March 2007 (r=0.80). We suggest that this is due to the ability of polonium to distinguish between bulk mass flux and organic carbon export under oligotrophic and lithogenic-driven flux regimes. Further, we found that the POC/Po ratio on particles was largely independent of size class between 10 and 100 μm (P=0.13) during each season, supporting the notion that export in this oligotrophic system is driven by sinking aggregates of smaller cells and not by large, individual cells.  相似文献   

7.
Ectohydrolase activities of suspended microbiota were compared to those associated with sinking particles (sed-POM) retrieved from sediment traps deployed in the permanently anoxic Cariaco Basin. In shore-based assays, activities of aminopeptidase, β-glucosidase, chitinase and alkaline phosphatase were measured in samples obtained from oxic and anoxic depths using MUF- and MCA-labeled fluorogenic substrate analogs. Hydrolysis potentials for these enzymes in the seston varied widely over the nine cruises sampled (8 Nov 1996–3 May 2000) and among depths (15–1265 m); from <10 to over 1600 nM d?1 hydrolysate released, generally co-varying with one another and with suspended particulate organic carbon (POC) and particulate nitrogen (PN). Hydrolytic potentials, prokaryotic abundances and POC/PN concentrations in sinking debris were 400–1.3×107 times higher than in comparable volumes of seawater. However when normalized to PN, hydrolytic potentials in sediment trap samples were not demonstrably higher than in Niskin bottle samples. We estimate that PN pools in sediment trap samples were turned over 2–1400 times (medians=7–26x) slower by hydrolysis than were suspended PN pools. Median prokaryotic growth rates (divisions d?1) in sinking debris were also ～150 times slower than for bacterioplankton. Hydrolytic potentials in surface oxic waters were generally faster than in underlying anoxic waters on a volumetric basis (nM hydrolysate d?1), but were not significantly (p>0.05) different when normalized to PN or prokaryote abundances. Alkaline phosphatase was consistently the most active ectohydrolase in both sample types, suggesting that Cariaco Basin assemblages were adapted to decomposing phosphate esters in organic polymers. However, phosphorus limitation was not evident from nutrient inventories in the water column. Results support the hypothesis that efficiencies of polymer hydrolysis in anoxic waters are not inherently lower than in oxic waters.  相似文献   

8.
Mass, carbon, and nitrogen fluxes and carbon and nitrogen compositions were determined for particulate samples from plankton net tows, shallow floating sediment traps, intermediate and deep moored sediment traps, and sediment cores collected along 140°W in the central equatorial Pacific Ocean during the US JGOFS EqPac program. Mass, particulate organic carbon (POC), and particulate inorganic carbon (PIC) fluxes measured by the floating sediment traps during the Survey I (El Niño) and Survey II (non-El Niño) cruises follow essentially the same pattern as primary production: high near the equator and decreasing poleward. POC fluxes caught in free-floating traps were compared with alternative estimates of export fluxes, including 234Th models, new production, and other sediment trap studies, resulting in widely differing estimates. Applying 234Th corrections to the trap-based fluxes yielded more consistent results relative to primary production and new production. Despite factors of five differences in measured fluxes between different trap types, POC : 234Th ratios of trap material were generally within a factor of two and provided a robust means of converting modeled 234Th export fluxes to POC export fluxes. All measured fluxes decrease with depth. Trap compositional data suggest that mineral “ballasting” may be a prerequisite for POC settling. POC remineralization is most pronounced in the epipelagic zone and at the sediment–water interface, with two orders of magnitude loss at each level. Despite seawater supersaturation with respect to calcium carbonate in the upper ocean, 80% of PIC is dissolved in the epipelagic zone. Given the time-scale differences of processes throughout the water column, the contrasting environments, and the fact that only 0.01% of primary production is buried, sedimentary organic carbon accumulation rates along the transect are remarkably well correlated to primary production in the overlying surface waters. POC to particulate total nitrogen (PTN) ratios for all samples are close to Redfield values, indicating that POC and PTN are non-selectively remineralized. This constancy is somewhat surprising given conventional wisdom and previous equatorial Pacific results suggesting that particulate nitrogen is lost preferentially to organic carbon.  相似文献   

9.
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   

10.
The abundance, carbon isotopic composition (Δ14C and δ13C), and lipid biomarker (alkenones and saturated fatty acids) distributions of suspended particulate organic matter were investigated at three stations centered on the 2000, 3000, and 3500 m isobaths over the New England slope in order to assess particulate carbon sources and dynamics in this highly productive and energetic region. Transmissometry profiles reveal that particle abundances exhibit considerable fine structure, with several distinct layers of elevated suspended particulate matter concentration at intermediate water depths in addition to the presence of a thick bottom nepheloid layer at each station. Excluding surface water samples, the Δ14C values of particulate organic carbon (POC) indicated the presence of a pre-aged component in the suspended POC pool (Δ14C<+38‰). The Δ14C values at the 3000 m station exhibited greater variability and generally were lower than those at the other two stations where the values decreased in a more systematic matter with increasing sampling depth. These lower Δ14C values were consistent with higher relative abundances of terrigenous long-chain fatty acids at this station than at the other two stations. Two scenarios were considered regarding the potential provenances of laterally transported POC: cross-shelf transport of shelf sediment (Δ14C=?140‰) and along-slope transport of the slope sediment proximal to the sampling locations (Δ14C=?260‰). Depending on the scenario, isotopic mass balance calculations indicate allochthonous POC contributions ranging between 15% and 54% in the meso- and bathy-pelagic zone, with the highest proportions at the 3000 m station. Alkenone-derived temperatures recorded on suspended particles from surface waters closely matched in-situ temperatures at each station. However, alkenone-derived temperatures recorded on particles from the subsurface layer down to 250 m were lower than those of overlying surface waters, especially at the 3000 m station, implying supply of phytoplankton organic matter originally produced in cooler surface waters. AVHRR images and temperature profiles indicate that the stations were under the influence of a warm-core ring during the sampling period. The low alkenone-derived temperatures in the subsurface layer coupled with the lower Δ14C values for the corresponding POC suggests supply of OC on resuspended sediments underlying cooler surface waters distal to the study area, possibly further north or west. Taken together, variations in Δ14C values, terrigenous fatty acid abundances, and alkenone-derived temperatures among the stations suggest that input of laterally advected OC is a prominent feature of POC dynamics on the NW Atlantic margin, and is spatially heterogeneous on a scale smaller than the distance between the stations (<150 km).  相似文献   

11.
To gain new insights into the variability of particulate organic carbon (POC) fluxes and to better understand the factors controlling the POC/234Th ratios in suspended and sinking particulate matter, we investigated the relationships between POC/234Th ratios and biochemical composition (uronic acids, URA; total carbohydrates, TCHO; acid polysaccharides, APS; and POC) of suspended and sinking matter from the Gulf of Mexico in 2005 and 2006. Our data show that URA/POC in sediment traps (STs), APS/POC in the suspended particles, and turnover times of particulate 234Th in the water column and those of bacteria in STs inside eddies usually increased with depth, whereas particulate POC/234Th (10–50 μm) and the sediment-trap parameters (POC flux, POC/234Th ratio, bacterial biomass, and bacterial production) decreased with depth. However, this trend was not the case for most biological parameters (e.g., phytoplankton and bacterial biomass) or for the other parameters at the edges of eddies or at coastal-upwelling sites.In general, the following relationships were observed: 1) 234Th/POC ratios in STs were correlated with APS flux, and these ratios in the 10–50 μm suspended particles also correlated with URA/POC ratios; 2) neither URA fluxes nor URA/POC ratios were significantly related to bacterial biomass; 3) the sum of two uronic acids (G2, glucuronic, and galacturonic acid, which composed most of the URA pool) was positively related to bacterial biomass; and 4) the POC/234Th ratios in intermediate-sized particles (10–50 μm) were close to those in sinking particles but much lower than those in > 50 μm particles. The results indicate that acid polysaccharides, though a minor fraction (~ 1%) of the organic carbon, act more likely as proxy compound classes that might contain the more refractory 234Th-binding biopolymer, rather than acting as the original 234Th “scavenger” compound. Moreover, these acid polysaccharides, which might first be produced by phytoplankton and then modified by bacteria, also influence the on-and-off “piggy-back” processes of organic matter and 234Th, thus causing additional variability of the POC/234Th in particles of different sizes.  相似文献   

12.
《Marine Chemistry》2007,103(1-2):185-196
Large-volume sampling of 234Th and drifting sediment trap deployments were conducted as part of the 2004 Western Arctic Shelf–Basin Interactions (SBI) spring (May 15–June 23) and summer (July 17–August 26) process cruises in the Chukchi Sea. Measurements of 234Th and particulate organic carbon (POC) export fluxes were obtained at five stations during the spring cruise and four stations during the summer cruise along Barrow Canyon (BC) and along a parallel shelf-to-basin transect from East Hanna Shoal (EHS) to the Canada Basin. 234Th and POC fluxes obtained with in situ pumps and drifting sediment traps agreed to within a factor of 2 for 70% of the measurements. POC export fluxes measured with in situ pumps at 50 m along BC were similar in spring and summer (average = 14.0 ± 8.0 mmol C m− 2 day− 1 and 16.5 ± 6.5 mmol C m− 2 day− 1, respectively), but increased from spring to summer at the EHS transect (average = 1.9 ± 1.1 mmol C m− 2 day− 1 and 19.5 ± 3.3 mmol C m− 2 day− 1, respectively). POC fluxes measured with sediment traps at 50 m along BC were also similar in both seasons (31.3 ± 9.3 mmol C m− 2 day− 1 and 29.1 ± 14.2 mmol C m− 2 day− 1, respectively), but were approximately twice as high as POC fluxes measured with in situ pumps. Sediment trap POC fluxes measured along the EHS transect also increased from spring to summer (3.0 ± 1.9 mmol C m− 2 day− 1 and 13.0 ± 6.4 mmol C m− 2 day− 1, respectively), and these fluxes were similar to the POC fluxes obtained with in situ pumps. Discrepancies in POC export fluxes measured using in situ pumps and sediment traps may be reasonably explained by differences in the estimated POC/234Th ratios that arise from differences between the techniques, such as time-scale of measurement and size and composition of the collected particles. Despite this variability, in situ pump and sediment trap-derived POC fluxes were only significantly different at a highly productive station in BC during the spring.  相似文献   

13.
Quantifying relative affinities of Po and Pb in different populations of marine particulate matter is of great importance in utilizing 210Po as a tracer for carbon cycling. We collected and analyzed water samples for the concentrations of dissolved and total 210Po and 210Pb from the upper 600 m of the water column at Bermuda Time-series Study site (September 1999–September 2000) to investigate their seasonality of concentrations and their activity ratio (210Po/210Pb activity ratio, AR). Sinking particles collected in sediment traps at depths of 500 m, 1500 m, and 3200 m from the Oceanic Flux Program (OFP) time-series sediment traps were analyzed over a period of 12 months (May 1999–May 2000). The objective was to compare the deficiencies of 210Po with respect to 210Pb in the water column to that measured in the sediment traps and to assess the relative affinities of Po and Pb with different particle pools.Inventories of 210Po in the upper 500 m water column varied by a factor of 2, indicating seasonal variations of particulate flux dominated the removal of 210Po. The 210Po/210Pb ARs in the dissolved phase were generally less than the secular equilibrium value (1.0) in the upper 600 m, while were generally greater than 1.0 in the particulate phase, indicating higher removal rates of 210Po relative to 210Pb by particulate matter. The measured fluxes of 210Po and 210Pb in the 500 m, 1500 m, and 3200 m traps increased with depth, while the 210Po/210Pb ARs decreased with depth except from May–August 1999. From the measured fluxes of 210Po and 210Pb at these three traps and the concentrations of 210Po and 210Pb in the water column, this region appears to be a sink for 210Pb which is likely brought-in by lateral advection.  相似文献   

14.
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   

15.
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   

16.
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   

17.
For the investigation of organic carbon fluxes reaching the seafloor, oxygen microprofiles were measured at 145 sites in different sub-regions of the Southern Ocean. At 11 sites, an in situ oxygen microprofiler was deployed for the measurement of oxygen profiles and the calculation of organic carbon fluxes. At four sites, both in situ and ex situ data were determined for high latitudes. Based on this data set as well as on previous published data, a relationship was established for the estimation of fluxes derived by ex situ measured O2 profiles. The fluxes of labile organic matter range from 0.5 to 37.1 mg C m?2 d?1. The high values determined by in situ measurements were observed in the Polar Front region (water depth of more than 4290 m) and are comparable to organic matter fluxes observed for high-productivity, upwelling areas like off West Africa. The oxygen penetration depth, which reflects the long-term organic matter flux to the sediment, was correlated with assemblages of key diatom species. In the Scotia Sea (～3000 m water depth), oxygen penetration depths of less than 15 cm were observed, indicating high benthic organic carbon fluxes. In contrast, the oxic zone extends down to several decimeters in abyssal sediments of the Weddell Sea and the southeastern South Atlantic. The regional pattern of organic carbon fluxes derived from microsensor data suggests that episodic and seasonal sedimentation pulses are important for the carbon supply to the seafloor of the deep Southern Ocean.  相似文献   

18.
The diffusive component of the particulate organic carbon (POC) export from the ocean's surface layer has been estimated using a combination of the mixed layer model and SeaWiFS ocean color data. The calculations were carried out for several example sites located in the North Atlantic over a 10-year time period (1998–2007). Satellite estimates of surface POC derived from ocean color were applied as an input to the model driven by local surface heat and momentum fluxes. For each year of the examined period, the diffusive POC flux was estimated at a 200 m depth. The highest flux is generally observed in the spring and fall seasons, when surface waters are weakly stratified. In addition, the model results demonstrate significant interannual and geographical variability of the flux. The highest diffusive POC flux occurs in the northern North Atlantic and the lowest in the subtropical region. The interannual variability of the diffusive POC flux is associated with mixed layer dynamics and underscores the importance of atmospheric forcing for POC export from the surface layer to the ocean's interior.  相似文献   

19.
Continuous surface measurements of temperature, salinity, fluorescence and optical backscattering were made during R/V Thompson cruise no. TN053 in the northern Arabian Sea (“Bio-Optical cruise”; October–November, 1995). The cruise covered the early NE monsoon period. Optical measurements involved alternate estimates of total backscattering and acidified backscattering approximately every 1.5–2 min (measured after addition of a weak acid to dissolve calcium carbonate). The difference between total and acidified backscattering equals “acid-labile backscattering”. Total and acid-labile backscattering were converted to the concentration of particulate organic carbon (POC) and particulate inorganic carbon (PIC; calcium carbonate), respectively, and discrete samples taken along the cruise track were used for calibration. Backscattering data were frequently coherent with temperature, salinity, and density variability. Acid-labile backscattering values revealed that calcium carbonate accounted for 10–40% of the total optical backscattering in the region, and the semi-continuous records demonstrated distinct patches of coccolith-rich water. The northern Arabian Sea had the highest acid-labile backscattering. Results suggest that PIC : POC ratios can vary over about four orders of magnitude. Highest surface values of PIC : POC approached one in several places. We also report qualitative observations of phytoplankton community structure made aboard ship, on fresh samples.  相似文献   

20.
Direct measurements of new production and carbon export in the subtropical North Atlantic Ocean appear to be too low when compared to geochemical-based estimates. It has been hypothesized that episodic inputs of new nutrients into surface water via the passage of mesoscale eddies or winter storms may resolve at least some of this discrepancy. Here, we investigated particulate organic carbon (POC), particulate organic nitrogen (PON), and biogenic silica (BSiO2) export using a combination of water column 234Th:238U disequilibria and free-floating sediment traps during and immediately following two weather systems encountered in February and March 2004. While these storms resulted in a 2–4-fold increase in mixed layer NO3 inventories, total chlorophyll a and an increase in diatom biomass, the systems were dominated by generally low 234Th:238U disequilibria, suggesting limited particle export. Several 234Th models were tested, with only those including non-steady state and vertical upwelling processes able to describe the observed 234Th activities. Although upwelling velocities were not measured directly in this study, the 234Th model suggests reasonable rates of 2.2–3.7 m d?1.Given the uncertainties associated with 234Th derived particle export rates and sediment traps, both were used to provide a range in sinking particle fluxes from the upper ocean during the study. 234Th particle fluxes were determined applying the more commonly used steady state, one-dimensional model with element/234Th ratios measured in sediment traps. Export fluxes at 200 m ranged from 1.91±0.20 to 4.92±1.22 mmol C m?2 d?1, 0.25±0.08 to 0.54±0.09 mmol N m?2 d?1, and 0.22±0.04 to 0.50±0.06 mmol Si m?2 d?1. POC export efficiencies (Primary Production/Export) were not significantly different from the annual average or from time periods without storms, although absolute POC fluxes were elevated by 1–11%. This increase was not sufficient, however, to resolve the discrepancy between our observations and geochemical-based estimates of particle export. Comparison of PON export rates with simultaneous measurements of NO3? uptake derived new production rates suggest that only a fraction, <35%, of new production was exported as particles to deep waters during these events. Measured bSiO2 export rates were more than a factor of two higher (p<0.01) than the annual average, with storm events contributing as much as 50% of annual bSiO2 export in the Sargasso Sea. Furthermore it appears that 65–95% (average 86±14%) of the total POC export measured in this study was due to diatoms.Combined these results suggest that winter storms do not significantly increase POC and PON export to depth. Rather, these storms may play a role in the export of bSiO2 to deep waters. Given the slower remineralization rates of bSiO2 relative to POC and PON, this transport may, over time, slowly decrease water column silicate inventories, and further drive the Sargasso Sea towards increasing silica limitation. These storm events may further affect the quality of the POC and PON exported, given the large association of this material with diatoms during these periods.  相似文献   

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