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1.
Using simultaneous sampling with a commercial-sized trawl, a zooplankton net, and a sediment trap, we evaluated the contribution of vertically migrating micronekton to vertical material transport (biological pump) at two stations (3°00′N, 146°00′E and 3°30′N, 145°20′E) in the western equatorial North Pacific. The gravitational sinking particulate organic carbon flux out of the euphotic zone was 54.8 mg C m−2 day−1. The downward active carbon flux by diel migrant mesozooplankton was 23.53 and 9.97 mg C m−2 day−1, and by micronekton 4.40 and 2.26mg C m−2 day−1 at the two stations. Assuming that the micronekton sampling efficiency of the trawl was 14%, we corrected the downward carbon flux due to micronekton respiration to 29.9 and 15.2mg C m−2 day−1, or 54.6 and 27.7% of the sinking particle flux at the two stations. The corrected micronekton gut fluxes were 1.53 and 0.97mg C m−2 day−1. The role of myctophid fish fecal matter as a possible food resource for deep-sea organisms, based on its fatty acid and amino acid analysis, is discussed.  相似文献   

2.
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   

3.
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   

4.
The suspended particulate organic matter (sPOM) around two isolated NE Atlantic seamounts, Seine (33°46′N 14°21′W; summit at ∼170 m) and Sedlo (40°19′N 26°40′W; summit at ∼780 m), was studied over a period of 2 years during four 2–4-week oceanographic surveys. Elemental (C and N), chlorophyll a and lipid biomarker concentrations and N stable isotopic values were variable close to the surface (40–90 m), although some chlorophyll a enrichment above the summits was discerned sporadically. Results from near-surface waters showed a generally “fresh”, mainly phytoplankton signature in sPOM with some seasonality, which was more pronounced around Sedlo. sPOM concentrations and composition changed with depth, apparently controlled by seasonality and proximity to the seamounts. A few metres above the Seine summit, the suspended particulate organic carbon (sPOC) concentrations and labile polyunsaturated fatty acids (% of lipids) were higher than elsewhere at similar depths (∼200 m) in summer 2004. In the same season at Sedlo, polyunsaturated fatty acids were also relatively more abundant (up to 43% of total lipids) around the topographic feature throughout the water column, indicating supply of more labile sPOM, perhaps by advection, downwelling or passive sinking of locally produced phytoplankton and/or in situ production. The high-quality sPOM that seems to be present around the seamounts could provide an important food source to the biological community.  相似文献   

5.
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   

6.
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   

7.
We discuss nitrous oxide (N2O) and methane (CH4) distributions in 49 vertical profiles covering the upper ∼300 m of the water column along two ∼13,500 km transects between ∼50°N and ∼52°S during the Atlantic Meridional Transect (AMT) programme (AMT cruises 12 and 13). Vertical N2O profiles were amenable to analysis on the basis of common features coincident with Longhurst provinces. In contrast, CH4 showed no such pattern. The most striking feature of the latitudinal depth distributions was a well-defined “plume” of exceptionally high N2O concentrations coincident with very low levels of CH4, located between ∼23.5°N and ∼23.5°S; this feature reflects the upwelling of deep waters containing N2O derived from nitrification, as identified by an analysis of N2O, apparent oxygen utilization (AOU) and NO3−, and presumably depleted in CH4 by bacterial oxidation. Sea-to-air emissions fluxes for a region equivalent to ∼42% of the Atlantic Ocean surface area were in the range 0.40–0.68 Tg N2O yr−1 and 0.81–1.43 Tg CH4 yr−1. Based on contemporary estimates of the global ocean source strengths of atmospheric N2O and CH4, the Atlantic Ocean could account for ∼6–15% and 4–13%, respectively, of these source totals. Given that the Atlantic Ocean accounts for around 20% of the global ocean surface, on unit area basis it appears that the Atlantic may be a slightly weaker source of atmospheric N2O than other ocean regions but it could make a somewhat larger contribution to marine-derived atmospheric CH4 than previously thought.  相似文献   

8.
A study was carried out to assess primary production and associated export flux in the coastal waters of the western Antarctic Peninsula at an oceanographic time-series site. New, i.e., exportable, primary production in the upper water-column was estimated in two ways; by nutrient deficit measurements, and by primary production rate measurements using separate 14C-labelled radioisotope and 15N-labelled stable isotope uptake incubations. The resulting average annual exportable primary production estimates at the time-series site from nutrient deficit and primary production rates were 13 and 16 mol C m−2, respectively. Regenerated primary production was measured using 15N-labelled ammonium and urea uptake, and was low throughout the sampling period.The exportable primary production measurements were compared with sediment trap flux measurements from 2 locations; the time-series site and at a site 40 km away in deeper water. Results showed ∼1% of the upper mixed layer exportable primary production was exported to traps at 200 m depth at the time-series site (total water column depth 520 m). The maximum particle flux rate to sediment traps at the deeper offshore site (total water column depth 820 m) was lower than the flux at the coastal time-series site. Flux of particulate organic carbon was similar throughout the spring–summer high flux period for both sites. Remineralisation of particulate organic matter predominantly occurred in the upper water-column (<200 m depth), with minimal remineralisation below 200 m, at both sites. This highly productive region on the Western Antarctic Peninsula is therefore best characterised as ‘high recycling, low export’.  相似文献   

9.
234Th was used to quantify sinking fluxes and residence times of particles in surface waters of the north-western Mediterranean Sea. Measurements of dissolved and particulate 234Th were made at the DYFAMED station (43°25′N–7°51′E, JGOFS-France program). Sampling covered 1 year on four cruises in 1994 (February 9, April 29, June 3, October 1) and focused on a transition period in mid-spring with six repeated profiles collected during May 1995. 234Th was nearly in equilibrium with its parent 238U most of the year, except in spring. The intensive sampling in May shows a rapid evolution throughout the month from a moderate 234Th deficit to near-equilibrium values. The time-series of 234Th were treated with steady-state and non-steady-state models. 234Th particulate fluxes clearly indicate large variability in export, with the highest values observed in spring. Particle residence times in the upper 40 m range from <10 to >250 days, and could increase by a factor of 10 within 2 weeks. POC fluxes from the upper 40 m and export ratios (ThE: ratio of 234Th-derived POC export to primary production), derived from the 234Th/238U disequilibrium in the water column and POC/234Th ratio on trapped material, decrease from about 9.5 mmol C m−2 d−1 and >22% in early May to less than 5 mmol C m−2 d−1 and 15% after mid-May. The 234Th-derived information is in agreement with the annual variations in Mediterranean Sea productivity.  相似文献   

10.
Bio-acoustic surveys and associated zooplankton net tows have documented anomalously high concentrations of zooplankton within a 100 m layer above the hydrothermal plumes at Endeavour Segment, Juan de Fuca Ridge. These and other data suggest that congregating epi-plume zooplankton are exploiting a food substrate associated with the hydrothermal plume. Ascending, organic-rich particles could provide a connection. Consequently, two paired sequentially sampling ascending and descending particle flux traps and a current meter were deployed on each of three moorings from July 1994 to May 1995. Mooring sites included an on-axis site (OAS; 47°57.0′N, 129°05.7′W) near the main Endeavour vent field, a “down-current” site 3 km west of the main vent field (WS), and a third background station 43 km northeast of the vent field (ES). Significant ascending and descending particle fluxes were measured at all sites and depths. Lipid analyses indicated that ascending POC was derived from mid-depth and deep zooplankton whereas descending POC also contained a component of photosynthetically derived products from the sea surface. Highest ascending POC fluxes were found at the hydrothermal plume-swept sites (OAS and WS). The limited data available, however, precludes an unequivocal conclusion that hydrothermal processes contribute to the ascending flux of organic carbon at each site. Highest ascending to descending POC flux ratios were also found at WS. Observed trends in POC, PMn/PTi, and PFe/PTi clearly support a hydrothermal component to the descending flux at the plume-swept WS site (no descending data was recovered at OAS) but not at the background ES site. Alternative explanations for ascending particle data are discussed. First-order calculations for the organic carbon input (5–22 mg C m−2 d−1) required to sustain observed epi-plume zooplankton anomalies at Endeavour are comparable both to measured total POC flux to epi-plume depths (2–5 mg C m−2 d−1: combined hydrothermal and surface derived organic carbon) and to estimates of the total potential in situ organic carbon production (2–9 mg C m−2 d−1) from microbial oxidation of hydrothermal plume H2, CH4 and NH4+.  相似文献   

11.
A 1-D coupled physical-biogeochemical model is used to study the seasonal cycles of silicon and nitrogen in two High Nutrient Low Chlorophyll (HNLC) systems, the Antarctic Circumpolar Current (ACC) and the North Pacific Ocean, and a mesotrophic system, the North Atlantic Ocean. The biological model consists of nine compartments (diatoms, nano-flagellates, microzooplankton, mesozooplankton, two types of detritus, nitrate, ammonium and silicic acid) forced by irradiance, temperature, mixing and deep nitrate and silicic acid concentrations. At all sites, nanophytoplankton standing crop variations are low, in spite of variations in primary production, because of a “top–down” control by microzooplankton. Although nanophytoplankton sustain more than 60% of the annual primary production in these areas, their contribution to the export production does not exceed 1% of the total. The differences in the seasonal plankton cycle among these regions come mainly from differences in the dynamics of large phytoplankton (here diatoms). In the ACC, the chlorophyll maximum remains <1.5 mg m−3, as an unfavourable light/mixing regime and a likely trace-metal limitation keep diatoms from blooming. In the northeast Pacific, trace-metal limitation seems to keep diatoms from blooming throughout the year. In both these systems, light or iron limitations induce high Si/N uptake ratios. Incidentally these high Si/N uptake ratios lead to a net excess of silicic acid utilization over nitrate, and to a subsequent silicic acid limitation during the summertime. In the North Atlantic, under favourable light/mixing regime and nutrient-replete conditions at the onset of the growing period, diatoms outburst and sustain a bloom >3.5 mg Chl-a m−3. Thereafter, mesozooplankton grazing pressure and silicic acid limitation induce the collapse of the chlorophyll maximum and the persistence of lower chlorophyll concentrations in summer. Although the ACC and the North Pacific show HNLC features, they support a high biogenic silica production (1.9 and 1.07 mol Si m−2 yr−1) and export flux (0.79 and 0.61 mol Si m−2 yr−1), compared to the North Atlantic (production: 0.23 mol Si m−2 yr−1, export: 0.12 mol Si m−2 yr−1). The differences in Si production and export between the HNLC systems and the mesotrophic North Atlantic come from both higher Si concentrations and Si/N uptake ratios in the HNLC areas compared to the North Atlantic. Also, the low dissolution rate of biogenic silica compared to nitrogen degradation rate, and the inhibition of nitrate uptake by ammonium, reinforce the net excess of silicic acid utilization over nitrate. As a result, the model also illustrates the efficiency of the silica pump for the three sites: about 50% of the biogenic silica synthesized in the euphotic layer is exported out of the first 100 m, while only 4–11% of the particulate organic nitrogen escapes recycling in the surface layer.  相似文献   

12.
In the framework of the German contribution to the Joint Global Ocean Flux Study (JGOFS), deep-water fluxes of particle-associated trace elements were measured in the northeast Atlantic Ocean. The sinking particles were collected almost continuously from 1992 to 1996 at three time-series stations, L1 (33°N/22°W), L2 (47°N/20°W), and L3 (54°N/21°W), using sediment traps. The focus of the present study is the temporal variability of the particle-associated elemental fluxes of Al, Ca, Cd, Co, Cu, Fe, Mn, Ni, P, Pb, Ti, V, and Zn at a depth of 2000 m.A clear seasonality of the fluxes that persisted for several years was documented for the southernmost station (L1) at stable oligotrophic conditions in the area of the North Atlantic Subtropical Gyre East (NASTE). At L2 and L3, an episodic nature of the elemental fluxes was determined. Mesoscale eddies are known to frequently cause temporal and spatial variability in the flux of biogenic components in that area. These events modified the simple seasonal pattern controlled by the annual cycle at L2, in the North Atlantic Drift Region (NADR), and at L3, which was influenced by the Atlantic Arctic province (ARCT). All stations were characterized by an additional episodic lithogenic atmospheric supply reaching the deep sea.The integrated annual fluxes during the multi-year study revealed similar flux magnitudes for lithogenic elements (Al, Co, Fe, Ti, and V) at L2 and L3 and roughly twofold fluxes at L1. Biogenic elements (Cd, P, and Zn) showed the opposite trend, i.e., two to fourfold higher values at L2 and L3 than at L1. For Mn, Ni, and Cu, the spatial differences were smaller, perhaps because of the intermediate behavior, between lithogenic and biogenic, of these elements. Similarly, among the three study sites, there were no noticeable differences in the total annual flux of Pb.The respective lithogenic fractions of the deep-sea fluxes of Cd, Co, Cu, Mn, Ni, V, and Zn were subtracted based on the amount of Al, with the average composition of the continental crust as reference. This procedure allowed estimation of the labile trace element fraction (TEexc) of the particles, i.e., TE taken up or scavenged during particle production and sedimentation. The ratios of TEexc/P clearly demonstrated an enrichment of TE over labile P from biogenic surface material to the deep sea for Zn (factor 4–6), Mn (12–27), Ni (3–5), and Cu (9–25); an intermediate status for Co (0.5–2.2); and depletion for Cd vs. P (0.2–0.4). Surprisingly, the recycling behavior of excess Co was found to be similar to that of P. Hence, Coexc behaved like a biogenic element; this is in contrast to total Co, which is dominated by the refractory lithogenic fraction.Moreover, it is argued that these excess elemental fluxes caused a loss of the dissolved elements in upper waters, since their transport reaches the deep-sea waters at 2000 m, a depth far below of deep-winter mixing and upwelling. The annual amount of excess TE exported from surface waters was estimated to be 1.3×109 mol Zn y?1, 4.4×109 mol Mn y?1, 4.9×108 mol Ni y?1, 2.2×107 mol Cd y?1, 7.4×108 mol Cu y?1, and 2.7×107 mol Co y?1 for the whole North Atlantic Ocean. Important primary sources that could replenish these losses are the aeolian and fluvial supply processes.  相似文献   

13.
Studies of nitrogen and phosphorus dynamics in the oligotrophic surface waters of the western North Atlantic Ocean have been constrained because ambient concentrations are typically at or below the detection limits of standard colorometric methods, except during periods of deep vertical mixing. Here we report the application of high-sensitivity analytical methods—determinations of nitrate plus nitrite (N+N) by chemiluminescence and soluble reactive phosphorus (SRP) by the magnesium induced co-precipitation (MAGIC) protocol—to surface waters along a transect from the Sargasso Sea at 26°N through the Gulf Stream at 37°N, including sampling at the JGOFS Bermuda Atlantic Time-series Study (BATS) station. The results were compared with data from the BATS program, and the HOT station in the Pacific Ocean, permitting cross-ecosystem comparisons. Microbial populations were analyzed along the transect, and an attempt was made to interpret their distributions in the context of the measured nutrient concentrations.Surface concentrations of N+N and SRP during the March 1998 transect separated into 3 distinct regions, with the boundaries corresponding roughly to the locations of the BATS station (∼31°N) and the Gulf Stream (∼37°N). Although N+N and SRP co-varied, the [N+N] : [SRP] molar ratios increased systematically from ∼1 to 10 in the southern segment, remained relatively constant at ∼40–50 between 31°N and 37°N, then decreased again systematically to ratios <10 north of the Gulf Stream. Dissolved organic N (DON) and P (DOP) dominated (⩾90%) the total dissolved N (TDN) and P (TDP) pools except in the northern portion of the transect. The [DON] : [DOP] molar ratios were relatively invariant (∼30–60) across the entire transect.Heterotrophic prokaryotes (operationally defined as “bacteria”), Prochlorococcus, Synechococcus, ultra- and nanophytoplankton, cryptophytes, and coccolithophores were enumerated by flow cytometry. The abundance of bacteria was well correlated with the concentration of SRP, and that of the ultra- and nanophytoplankton was well correlated with the concentration of N+N. The only group whose concentration was correlated with temperature was Prochlorococcus, and its abundance was unrelated to the concentrations of nutrients measured at the surface.We combined our transect results with time-series measurements from the BATS site and data from select depth profiles, and contrasted these North Atlantic data sets with time-series of N and P nutrient measurements from a station in the North Pacific subtropical gyre near Hawaii [Hawaii Ocean Time-series (HOT) site]. Two prominent differences are readily observed from this comparison. The [N+N] : [SRP] molar ratios are much less than 16 : 1 during stratified periods in surface waters at the BATS site, as is the case at the HOT site year round. However, following deep winter mixing, this ratio is much higher than 16 : 1 at BATS. Also, SRP concentrations in the upper 100 m at BATS fall in the range 1–10 nM during stratified periods, which is at least one order of magnitude lower than at the HOT site. That two ecosystems with comparable rates of primary and export production would differ so dramatically in their nutrient dynamics is intriguing, and highlights the need for detailed cross ecosystem comparisons.  相似文献   

14.
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   

15.
Sediment traps were deployed for almost 1 yr at two sites near 178°40′E in 1996–1997 on Chatham Rise (New Zealand). These sites were either side of the Subtropical Front (STF), which is a biologically productive zone, characterised by moderate atmospheric CO2 uptake. At each site, PARFLUX sediment traps (Mk 7G–21) were deployed at 300 and 1000 m in 1500 m water depth. At 42°42′S, north of the STF, approximately 80% of the integrated total mass, POC and biogenic silica flux at 300 m occurred in a 7-day pulse in austral mid-spring (1064, 141 and 6 mg m−2 d−1, respectively, in early October). This pulse was recorded a week later in the 1000 m trap, indicating a particle sinking rate of 100 m d−1. In contrast, at 44°37′S, south of the STF, the main flux of total mass and biogenic silica occurred 3 weeks later in late spring (289 and 3 mg m−2 d−1, respectively, in early November). Organic carbon, nitrogen and phosphorus fluxes were persistently high over spring at the southern site, although total POC flux integrated over 3 months was only 60 mg m−2 d−1. Thus, up to 2–3 times more material was exported north of the STF, compared with fluxes measured <200 km away to the south. As an integrated proportion of the annual total mass flux, however, more organic carbon was exported south of the STF (17% cf. 5–14%). Furthermore, organic material exported in spring from southern waters was labile and protein-rich (C : N — 8–16, C : P — 200–450, N : P — 13–36), compared to the more refractory, diatom-dominated material sinking out north of the STF in spring (C : N 9–22, C : P 50–230, N : P 5–19). These observations are consistent with anomalously high benthic biomass and diversity observed on south Chatham Rise. Resuspension and differential particle settling are probable causes for depth increases in particulate flux. Estimated particle source areas may be up to 120 km away due to high levels of mesoscale activity and mean flow in the STF region.  相似文献   

16.
Three time-series sediment traps were deployed in the Japan Trench at 40°26′N, 144°28′E, from October 1994 to May 1995. The depths were approximately 1, 4.2 and 6.8 km and the water depth was 7150 m. There were large mass fluxes in spring at 1 and 4.2 km depths, whereas increased fluxes appeared from 27 December 1994 to 29 January 1995, at 4.2 and 6.8 km depths. The 1994 Sanriku-Oki earthquake (Mw=7.7) occurred on 28 December 1994, at 40°27′N, 143°43′E, adjacent to the study site. Distinct increases in non-biogenic material were observed at both 4.2 and 6.8 km just after the earthquake; the material seems to have originated from the surface sediments, though differing Mn/Al of particulate materials at the two depths imply a difference in their source areas. Analysis indicates that the main part of the increased particulate fluxes at 6.8 km depth derived from the sediment on the eastern slope of the Japan Trench.  相似文献   

17.
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   

18.
The effects of extreme atmospheric forcing on the export flux of particulate organic carbon (POC) in the warm oligotrophic nitrogen-limited northwest Pacific Ocean were examined in 2007 during the spring Asian dust storm period. Several strong northeast monsoon events (maximum sustained wind speeds approaching 16.7 m s? 1, and gusts up to 19.0 m s? 1) accompanied by dust storms occurred during a 1-month period. The cold stormy events decreased surface water temperature and induced strong wind-driven vertical mixing of the water column, resulting in nutrient entrainment into the mixed layer from subsurface waters. As a result, the export flux of POC ranged from 49 to 98 (average value = 71 ± 16) mg m? 2 day? 1, approximately 2–3 times greater than average values in other seasons. As dry and wet deposition of nitrogen attributable to Asian dust storm events does not account for the associated increases in POC stocks in this N-limited oligotrophic oceanic region, the enhancement of POC flux must have been caused by nutrient entrainment from subsurface waters because of the high winds accompanying the dust storm events.  相似文献   

19.
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   

20.
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   

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