首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 31 毫秒
1.
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   

2.
Measurements of 234Th/238U disequilibria and particle size-fractionated (1, 10, 20, 53, 70, 100 μm) organic C and 234Th were made to constrain estimates of the export flux of particulate organic C (POC) from the surface waters of the Ligurian, Tyrrhenian and Aegean Seas in March–June 2004. POC exported from the surface waters (75–100 m depth) averaged 9.2 mmol m−2 d−1 in the Ligurian and Tyrrhenian Seas (2.3±0.5–14.9±3.0 mmol m−2 d−1) and 0.9 mmol m−2 d−1 in the Aegean Sea. These results are comparable to previous measurements of 234Th-derived and sediment-trap POC fluxes from the upper 200 m in the Mediterranean Sea. Depth variations in the POC/234Th ratio suggest two possible controls. First, decreasing POC/234Th ratios with depth were attributed to preferential remineralization of organic C. Second, the occurrence of maxima or minima in the POC/234Th ratio near the DCM suggests influence by phytoplankton dynamics. To assess the accuracy of these data, the empirical 234Th-method was evaluated by quantifying the extent to which the 234Th-based estimate of POC flux, PPOC, deviates from the true flux, FPOC, defined as the p-ratio (p-ratio=PPOC/FPOC=STh/SPOC, where S=particle sinking rate). Estimates of the p-ratio made using Stokes’ Law and the particle size distributions of organic C and 234Th yield values ranging from 0.93–1.45. The proximity of the p-ratio to unity implies that differences in the sinking rates of POC- and 234Th-carrying particles did not bias 234Th-normalized POC fluxes by more than a factor of two.  相似文献   

3.
《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   

4.
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   

5.
The phase partitioning of 234Th between dissolved (<10-kiloDalton, kD), colloidal (10 kD—0.4 μm), and particulate (⩾0.5 μm) matter across a horizontal transect, from a coastal station to the deep Canada Basin, and a vertical profile in the deep Canada Basin of the western Arctic Ocean was investigated. Concentrations of suspended particulate matter (SPM), dissolved, colloidal and particulate organic carbon, particulate organic nitrogen and nutrients (silicate, phosphate and nitrate) were also measured to assess transport and scavenging processes.Total 234Th (colloidal+particulate+dissolved) indicated deficiencies relative to secular equilibrium with its parent, 238U in the upper 100 m, which suggests active scavenging of 234Th onto particle surfaces. In contrast, at depths >200 m, general equilibrium existed between total 234Th and 238U. The inventory of SPM and the specific activity of particulate 234Th in the Canada Basin was about an order of magnitude higher than the profile reported for the Alpha Ridge ice camp station. This higher concentration of SPM in the southwestern Canada Basin is likely derived from ice-rafted sedimentary particles. Inventories of nutrients, and dissolved organic carbon and nitrogen in the upper 100 m of the Canada Basin are comparable to the other estimates for the central Arctic Ocean. Comparison of the mass concentrations of colloidal and filter-retained particulate matter as well as the activity of 234Th in these phases indicates that only a very small component of the colloidal material is actively involved in Th scavenging. Lower values of the conditional partition coefficient between the colloidal and dissolved phase indicate that the Arctic colloids are less reactive than colloidal material from other regions. The conditional partition coefficient between the filter-retained and dissolved phases (Kf) is generally higher than that for other regions, which is attributed to the higher complexation capacity of glacio-marine sedimentary particles in these waters. The 234Th-derived export of POC for the shelf and deep Canada Basin ranges between 5.6 and 6.5 mmol m−2 d−1, and is in agreement with other estimates reported for the central Arctic Ocean and Beaufort Sea.  相似文献   

6.
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   

7.
An extensive 234Th data set was collected at two sites in the North Pacific: ALOHA, an oligotrophic site near Hawaii, and K2, a mesotrophic HNLC site in the NW Pacific as part of the VERTIGO (VERtical Transport In the Global Ocean) study. Total 234Th:238U activity ratios near 1.0 indicated low particle fluxes at ALOHA, while 234Th:238U ~0.6 in the euphotic zone at K2 indicated higher particle export. However, spatial variability was large at both sites—even greater than seasonal variability as reported in prior studies. This variability in space and time confounds the use of single profiles of 234Th for sediment trap calibration purposes. At K2, there was a decrease in export flux and increase in 234Th activities over time associated with the declining phase of a summer diatom bloom, which required the use of non-steady state models for flux predictions. This variability in space and time confounds the use of single profiles of 234Th for sediment trap calibration purposes. High vertical resolution profiles show narrow layers (20–30 m) of excess 234Th below the deep chlorophyll maximum at K2 associated with particle remineralization resulting in a decrease in flux at depth that may be missed with standard sampling for 234Th and/or with sediment traps. Also, the application of 234Th as POC flux tracer relies on accurate sampling of particulate POC/234Th ratios and here the ratio is similar on sinking particles and mid-sized particles collected by in-situ filtration (>10–50 μm at ALOHA and >5–350 μm at K2). To further address variability in particle fluxes at K2, a simple model of the drawdown of 234Th and nutrients is used to demonstrate that while coupled during export, their ratios in the water column will vary with time and depth after export. Overall these 234Th data provide a detailed view into particle flux and remineralization in the North Pacific over time and space scales that are varying over days to weeks, and 10's–100's km at a resolution that is difficult to obtain with other methods.  相似文献   

8.
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   

9.
Dynamics of the natural radioactive particle tracer 234Th (half-life: 24.1 days) within the abyssal water column up to 1000 m above bottom and within surface sediments of the northeast Atlantic (Porcupine Abyssal Plain; depth: ≈4845 m) were investigated. Distributions of transmissometer voltages and potential temperature indicated a subdivision of the near-bottom water column into a benthic mixed layer (BML; thickness: ≈10–65 m) and the layer above the BML up to the upper boundary of the bottom nepheloid layer (BNL; thickness: ≈1000 m). Comparison of 234Th fluxes (dpm m−2d−1) in sediment traps, vertical fluxes derived from 234Th/238U-disequilibrium in the near-bottom water column and excess 234Th inventories in the surface sediment provided evidence for lateral advection of 234Th-depleted water and a ‘missing sink’ for 234Th. A simple one-dimensional steady-state box-model approach was applied to investigate 234Th dynamics. Estimated residence times suggest the BML and the resuspension zone of the surface sediment to be highly dynamic systems with respect to particle cycling and sorptive reactions on a time scale of weeks. Model results indicate that, through the chemical forcing of changing particle concentration, a thickening BML results in (1) increasing residence times of particulate 234Th in the BML with respect to the net fluxes across the upper boundary of the BML and into the surface sediment; (2) declining adsorption rate constants in the BML; (3) increasing desorptive fluxes in the BML resulting in (4) enhanced 234Th decay in the BML; (5) decreasing net fluxes of particulate 234Th from the BML to the upper BNL above the BML and to the sediment. Potential consequences for carbon cycling in the water column of the deep ocean are discussed.  相似文献   

10.
Depth profiles of total 234Th (dissolved+particulate) were collected at Station ALOHA (22°45N, 158°00W) in the North Pacific Subtropical Gyre during 9 cruises from April 1999 to March 2000. Samples were collected and processed by a new 2 L technique that enables more detailed depth resolution then previous 234Th studies. Significant zones of particle export (234Th deficiency) and particle remineralization (234Th excess) were measured both temporally and with depth. 234Th derived particulate carbon (PC) and nitrogen (PN) fluxes were determined with steady-state and non-steady-state models and PC/234Th and PN/234Th ratios measured with both in situ pumps and free-drifting particle interceptor traps deployed at 150 m. 234Th based export estimates of 4.0±2.3 mmol C m−2 d−1 and 0.53±0.19 mmol N m−2 d−1, were approximately 60% higher than those measured in PIT style sediment traps from the same time period, 2.4±0.2 mmol C m−2 d−1 and 0.32±0.08 mmol N m−2 d−1. Most of this difference is attributable to two large export events that occurred during October and December 1999, when traps undercollected for 234Th by a factor of 2 to 4. 234Th export (ThE) ratios based on 234Th derived PC flux/14C based primary production ranged from 4% to 22% (average=8.8%). Our results confirm the recent estimates of C export by Emerson et al. (Nature 389 (1997) 951) and Sonnerup et al. (Deep-Sea Research I 46 (1999) 777) and indicate that C export from the oligotrophic ocean must be considered when discussing C sequestration in global climate change.  相似文献   

11.
Seasonal changes in Th scavenging and particle aggregation were determined along two shelf-basin transects in the western Arctic Ocean during the spring (May–June) and summer (July–August) of 2002 and 2004. Measurements of dissolved and particulate 234Th and 228Th activities were used to quantify Th residence times and reversible rates of Th sorption and particle aggregation. Prior to the spring bloom in 2002, 234Th and 228Th residence times were equal and Th scavenging was concordant, indicating predominately steady-state conditions. In contrast, scavenging of 234Th and 228Th in the summer of 2002 and the spring and summer of 2004 was discordant, indicating a departure in scavenging rates from steady-state conditions during periods of seasonally high biological activity and particle export. Rates of particle aggregation and disaggregation were calculated using a one-dimensional reversible exchange model and 234Th and 228Th activities in small (1–53 μm) and large (>53 μm) particles. Maximum rates were determined coincident with the chlorophyll maximum (25–100 m) and increased by an order of magnitude between periods of low and high productivity. These Th measurements provide evidence that seasonally enhanced rates of particle aggregation might increase the magnitude of the particulate organic carbon (POC) flux in this Arctic regime.  相似文献   

12.
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   

13.
Sinking particles were collected every 4 h with drifting sediment traps deployed at 200 m depth in May 1995 in a 1-D vertical system during the DYNAPROC observations in the northwestern Mediterranean sea. POC, proteins, glucosamine and lipid classes were used as indicators of the intensity and quality of the particle flux. The roles of day/night cycle and wind on the particle flux were examined. The transient regime of production from late spring bloom to pre-oligotrophy determined the flux intensity and quality. POC fluxes decreased from, on average, 34 to 11 mg m−2 d−1, representing 6–14% of the primary production under late spring bloom conditions to 1–2% under pre-oligotrophic conditions. Total protein and chloroplast lipid fluxes correlated with POC and reflected the input of algal biomass into the traps. As the season proceeded, changes in the biochemical composition of the exported material were observed. The C/N ratio rose from 7.8 to 12. Increases of serine (10–28% of total proteins), total lipids (7–9 to 14–28% of POC) and reserve lipids (1–5 to 5–22% of total lipids) were noticeable, whereas total protein content in POC decreased (20–27 to 18–7%). N-acetyl glucosamine, a tracer of fecal pellet flux, showed that zooplankton grazing was a major vector of downward export during the decaying bloom. Against this background pattern, episodic events specifically increased the flux, modifying the quality and the settling velocity of particles. Day/night signals in biotracers (POC, N-acetyl glucosamine, protein and chloroplast lipids) showed that zooplankton migrations were responsible for sedimentation of fresh material through fast sinking particles (V=170–180 m d−1) at night. Periodic signatures of re-processed material (high lipolysis and bacterial biomass indices) suggested that other zooplankton fecal pellets or small aggregates, probably of lower settling velocities (V<170 m d−1), contributed to the flux during calm periods. At the beginning of the experiment, during the development of a prymnesiophyte bloom in the upper layers, the sterol signal with no periodicity enabled us to estimate high particle settling velocities (⩾600 m d−1) likely related to large aggregate formation. A wind event increased biotracer fluxes (POC, protein, chloroplast lipids). The rapid transmission of surface signals through extremely fast sinking particles could be a general feature of particle fluxes in marine areas unaffected by horizontal advection.  相似文献   

14.
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   

15.
234Th (T1/2=24.1 d) and 210Po (T1/2=138.4 d) are particle reactive radioisotopes that are used as tracers for particle cycling in the upper ocean. Particulate organic carbon (POC) export has frequently been estimated using 234Th/238U disequilibrium. Recent evidence suggests that 210Po/210Pb disequilibrium may be used as an additional tool to examine particle export, given the direct biological uptake of 210Po into cellular material. Differences in these two radioisotope pairs with regard to their half-lives, particle reactivity and scavenging affinity in seawater should provide complementary information to be obtained on the processes occurring in the water column. Here, we review eight different studies that have simultaneously used both approaches to estimate POC export fluxes from the surface ocean. Our aim is to provide a complete “dataset” of all the existing POC flux data derived from the coupled use of both 234Th and 210Po and to evaluate the advantages and limitations of each tracer pair. Our analysis suggests that the simultaneous use of both radiotracers provides more useful comparative data than can be derived from the use of a single tracer alone. The difference in half-lives of 234Th and 210Po enables the study of export production rates over different time scales. In addition, their different biogeochemical behaviour and preferred affinity for specific types of particles leads to the conclusion that 234Th is a better tracer of total mass flux, whereas 210Po tracks POC export more specifically. The synthesis presented here is also intended to provide a basis for planning future sampling strategies and promoting further work in this field to help reveal the more specific application of each tracer under specific water column biogeochemistries.  相似文献   

16.
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   

17.
We utilized 234Th, a naturally occurring radionuclide, to quantify the particulate organic carbon (POC) export rates in the northern South China Sea (SCS) based on data collected in July 2000 (summer), May 2001 (spring) and November 2002 (autumn). Th-234 deficit was enhanced with depth in the euphotic zone, reaching a subsurface maximum at the Chl-a maximum in most cases, as commonly observed in many oceanic regimes. Th-234 was in general in equilibrium with 238U at a depth of ∼100 m, the bottom of the euphotic zone. In this study the 234Th deficit appeared to be less significant in November than in July and May. A surface excess of 234Th relative to 238U was found in the summer over the shelf of the northern SCS, most likely due to the accumulation of suspended particles entrapped by a salinity front. Comparison of the 234Th fluxes from the upper 10 m water column between 2-D and traditional 1-D models revealed agreement within the errors of estimation, suggesting the applicability of the 1-D model to this particular shelf region. 1-D model-based 234Th fluxes were converted to POC export rates using the ratios of bottle POC to 234Th. The values ranged from 5.3 to 26.6 mmol C m−2d−1 and were slightly higher than those in the southern SCS and other oligotrophic areas. POC export overall showed larger values in spring and summer than in autumn, the seasonality of which was, however, not significant. The highest POC export rate (26.6 mmol C m−2d−1) appeared at the shelf break in spring (May), when Chl-a increased and the community structure changed from pico-phytoplankton (<2 μm) dominated to nano-phytoplankton (2–20 μm) and micro-phytoplankton (20–200 μm) dominated.  相似文献   

18.
The natural isotope 234Th is used in a small-scale survey of particle transport and exchange processes at the sediment–water interface in the Benguela upwelling area. Results from water and suspended particulate matter (SPM) samples from the uppermost and lowermost water column as well as the underlying sediment of three stations are compared. The stations are situated in different sedimentological environments at 1200–1350 m water depth at the continental slope off Namibia. Highly differing extent and particle content of the bottom nepheloid layer (BNL) are determined from transmissometer data. Three models are presented, all explaining the 234Th depletion of the BNL and 234Th excess of the surface sediment that were observed. While the first model is based solely on local resuspension of surface sediment particles, the second evaluates the influence of vertical particle settling from the surface waters on the 234Th budget in the BNL. The third model explains 234Th depletion in the BNL by sedimentation of particles that were suspended in the BNL during long-range transport. Particle inventory of the BNL is highest at a depocenter of organic matter at 25.5°S, where strong deposition is presently taking place and lateral particle transport is suggested to predominate sediment accumulation. This is supported by the high settling flux of particles out of the BNL into the sediments of the depocenter, exceeding the vertical particle flux into sediment traps at intermediate depth in the same area by up to an order of magnitude. High particle residence/removal times in the BNL above the depocenter in the range of 5–9 weeks support this interpretation. Comparison with carbon mineralization rates that are known from the area reveals that, notwithstanding the large fraction of advected particles, organic carbon flux into the surface sediment is remineralized to a large extent. The deployment of a bottom water sampler served as an in situ resuspension experiment and provided the first data of 234Th activity on in situ resuspended particles. We found a mean specific activity of 86 disintegrations per minute (dpm) g−1 (39–339 dpm g−1), intermediate between the high values for suspended particles (in situ pump: 580–760 dpm g−1; CTD rosette: 870–1560 dpm g−1) and the low values measured at the sediment surface (26–37 dpm g−1). This represents essential information for the modeling of 234Th exchange processes at the sediment–water interface.  相似文献   

19.
The West Spitsbergen Current, flowing northward through Fram Strait, causes a benthic nepheloid layer (BNL) on the western slope of the Yermak Plateau. This BNL is weaker on the eastern side of the Plateau and absent on the Greenland side of the Fram Strait, where the East Greenland Current flows south. In this BNL we find throughout a depletion of 234Th relative to its parent 238U, and we use this to study the particle dynamics in the BNL. The export flux from the ice-covered surface ocean and from a young bloom found in the ice-free waters off NE Greenland is shown to be negligible, allowing us to explain the 234Th depletion by interaction with the sediment alone. The depletion, balanced by a similar excess in the surface layer of the sediment, implies the existence of a settling-resuspension loop with an average particle residence time of 1–2 months. The asymmetry with a stronger resuspension loop on the western (80–120 mg m−2 d−1) than on the eastern side of the Yermak Plateau (1–15 mg m−2 d−1) is reflected in the numbers of species and individuals of suspension feeders in box core samples, and in epifauna densities estimated from video observations. The suspension feeders thus contribute to deposition of particles that are advected from more productive ice-free regions. This explanation is in agreement with the east–west asymmetry in the input of organic material to the sediments of the Yermak Plateau, which has been concluded from the distribution of pigments, bacterial activity and meiofauna abundances, observed in a concurrent study at the same stations. On the West Spitsbergen shelf, a very intensive BNL was monitored over 1 month with a moored filtration system. A part of the sustained high suspended load may be advected over long distances. This study illustrates how the tracer 234Th can help to determine the extent to which suspended particles are in continuous exchange with the seafloor, and where biological mediation and chemical modification can be expected.  相似文献   

20.
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   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号