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 46 毫秒
1.
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   

2.
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   

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.
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   

5.
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   

6.
Organic carbon fluxes through the sediment/water interface in the high-latitude North Atlantic were calculated from oxygen microprofiles. A wire-operated in situ oxygen bottom profiler was deployed, and oxygen profiles were also measured onboard (ex situ). Diffusive oxygen fluxes, obtained by fitting exponential functions to the oxygen profiles, were translated into organic carbon fluxes and organic carbon degradation rates. The mean Corg input to the abyssal plain sediments of the Norwegian and Greenland Seas was found to be 1.9 mg C m−2 d−1. Typical values at the seasonally ice-covered East Greenland continental margin are between 1.3 and 10.9 mg C m−2 d−1 (mean 3.7 mg C m−2 d−1), whereas fluxes on the East Greenland shelf are considerably higher, 9.1–22.5 mg C m−2 d−1. On the Norwegian continental slope Corg fluxes of 3.3–13.9 mg C m−2 d−1 (mean 6.5 mg C m−2 d−1) were found. Fluxes are considerably higher here compared to stations on the East Greenland slope at similar water depths. By repeated occupation of three sites off southern Norway in 1997 the temporal variability of diffusive O2 fluxes was found to be quite low. The seasonal signal of primary and export production from the upper water column appears to be strongly damped at the seafloor. Degradation rates of 0.004–1.1 mg C cm−3 a−1 at the sediment surface were calculated from the oxygen profiles. First-order degradation constants, obtained from Corg degradation rates and sediment organic carbon content, are in the range 0.03–0.6 a−1. Thus, the corresponding mean lifetime of organic carbon lies between 1.7 and 33.2 years, which also suggests that seasonal variations in Corg flux are small. The data presented here characterize the Norwegian and Greenland Seas as oligotrophic and relatively low organic carbon deep-sea environments.  相似文献   

7.
Whereas diatoms (class Bacillariophyceae) often dominate phytoplankton taxa in the Amazon estuary and shelf, their contribution to phytoplankton dynamics and impacts on regional biogeochemistry are poorly understood further offshore in the western tropical Atlantic Ocean (WTAO). Thus, relative contribution of diatoms to phytoplankton biomass and primary production rates and associated environmental conditions were quantified during three month-long cruises in January–February 2001, July–August 2001, and April–May 2003. The upper water column was sampled at 6 light depths (100%, 50%, 25%, 10%, 1% and 0.1% of surface irradiance) at 64 stations between 3° and 14°N latitude and 41° and 58°W longitude. Each station was categorized as ‘oceanic’ or ‘plumewater’, based on principal component analysis of eight physical, chemical and biological variables. All stations were within the North Brazil Current, and plumewater stations were characterized by shallower mixed layers with lower surface salinities and higher dissolved silicon (dSi) concentrations than oceanic stations. The major finding was a much greater role of diatoms in phytoplankton biomass and productivity at plumewater stations relative to oceanic stations. Mean depth-integrated bSi concentrations at the plumewater and oceanic stations were 14.2 and 3.7 mmol m−2, respectively. Mean depth-integrated SiP rates at the plumewater and oceanic stations were 0.17 and 0.02 mmol m−2 h−1, respectively. Based on ratios of SiP and PP rates, and typical Si:C ratios, diatoms contributed on average 29% of primary productivity at plumewater stations and only 3% of primary productivity at oceanic stations. In contrast, phytoplankton biomass (as chlorophyll a concentrations) and primary production (PP) rates (as 14C uptake rates) integrated over the euphotic zone were not significantly different at plumewater and oceanic stations. Chlorophyll a concentrations ranged from 8.5 to 42.4 mg m−2 and 4.0 to 38.0 mg m−2 and PP rates ranged from 2.2 to 11.2 mmol m−2 h−2 and 1.8 to 10.8 mmol m−2 h−2 at plumewater and oceanic stations, respectively. A conservative estimate of annual integrated SiP in offshore waters of Amazon plume between April and August is 0.59 Tmol Si, based on mean SiP rates in plumewaters and satellite-derived estimates of the area of the Amazon plume. In conclusion, river plumewaters dramatically alter the silicon dynamics of the WTAO, forming extensive diatom-dominated phytoplankton blooms that may contribute significantly to the global Si budget as well as contributing to energy and matter flow off of the continental shelf.  相似文献   

8.
The total organic carbon (TOC) and total inorganic carbon (CT) exchange between the Atlantic Ocean and the Mediterranean Sea was studied in the Strait of Gibraltar in September 1997. Samples were taken at eight stations from western and eastern entrances of the Strait and at the middle of the Strait (Tarifa Narrows). TOC was analyzed by a high-temperature catalytic oxidation method, and CT was calculated from alkalinity–pHT pairs and appropriate thermodynamic relationships. The results are used in a two-layer model of water mass exchange through the Strait, which includes the Atlantic inflow, the Mediterranean outflow and the interface layer in between. Our observations show a decrease of TOC and an increase of CT concentrations from the surface to the bottom: 71–132 μM C and 2068–2150 μmol kg−1 in the Surface Atlantic Water, 74–95 μM C and 2119–2148 μmol kg−1 in the North Atlantic Central Water, 63–116 μM C and 2123–2312 μmol kg−1 in the interface layer, and 61–78 μM C and 2307–2325 μmol kg−1 in the Mediterranean waters. However, within the Mediterranean outflow, we found that the concentrations of carbon were higher at the western side of the Strait (75–78 μM C, 2068–2318 μmol kg−1) than at the eastern side (61–69 μM C, 2082–2324 μmol kg−1). This difference is due to the mixing between the Atlantic inflow and the Mediterranean outflow on the west of the Strait, which results in a flux of organic carbon from the inflow to the outflow and an opposite flux of inorganic carbon. We estimate that the TOC input from the Atlantic Ocean to the Mediterranean Sea through the Strait of Gibraltar varies from (0.97±0.8)104 to (1.81±0.90)104 mol C s−1 (0.3×1012 to 0.56×1012 mol C yr−1), while outflow of inorganic carbon ranges from (12.5±0.4)104 to (15.6±0.4)104 mol C s−1 (3.99–4.90×1012 mol C yr−1). The high variability of carbon exchange within the Strait is due to the variability of vertical mixing between inflow and outflow along the Strait. The prevalence of organic carbon inflow and inorganic carbon outflow shows the Mediterranean Sea to be a basin of active remineralization of organic material.  相似文献   

9.
Benthic fluxes of O2, titration alkalinity (TA), total inorganic carbon (TIC), Ca2+, NO3, NH4+, PO43−, and Si(OH)4 were measured by in situ benthic flux chamber incubations at 13 locations on the North Carolina continental slope. The majority of measurements were made at water depths of approximately 700–850 m, in the previously identified upper slope depocenter. This region is characterized by extremely high organic matter deposition rates and near saturation bottom water oxygen concentrations. Measured benthic fluxes of TA are reasonably correlated with O2 benthic fluxes. Because bottom waters are supersaturated with respect to calcite and aragonite at these shallow water depths, these results demonstrate the importance of metabolically driven dissolution in this region. Subtraction of the calcium carbonate dissolution contributions from the TIC benthic fluxes suggests rates of organic matter remineralization ranging from 0.97 to 3.9 mol C m−2 yr−1 at the depocenter sites, a factor of 3–10 greater than estimated for the adjacent continental rise and upper slope areas. Because biological primary production in the overlying waters does not follow this pattern, these extremely high values are most likely supported by lateral inputs of highly reactive organic matter. Mass balance calculations indicate that despite the oxygenated bottom water conditions, 68% of the organic nitrogen released during organic matter remineralization processes is ultimately denitrified. The release of PO43− from the depocenter sediments is equivalent to or larger than that predicted from the remineralization of Redfield organic matter. This implies either that PO43− is preferentially released in this setting and that the accumulating sediments must be depleted in PO43− relative to organic carbon or that another, non-organic, phase is contributing PO43− to the system. The molar ratio of the Si benthic flux and organic carbon remineralization rate ranges from 0.30 to 0.86. This is significantly greater than the ratio reported for most pelagic diatoms. Possible reasons for this high ratio include the deposition of benthic diatoms that may have a larger Si : C ratio than pelagic diatoms, the near-bottom lateral input of partially reworked organic matter that may have an elevated Si : C ratio relative to fresh diatoms, preferential loss of carbon in sinking particulates or the release of Si from non-opaline materials.  相似文献   

10.
Dissolved oxygen (DO) in the ocean is a tracer for most ocean biogeochemical processes including net community production and remineralization of organic matter which in turn constrains the biological carbon pump. Knowledge of oxygen dynamics in the North Atlantic Ocean is mainly derived from observations at the Bermuda Atlantic Time-series Study (BATS) site located in the western subtropical gyre which may skew our view of the biogeochemistry of the subtropical North Atlantic. This study presents and compares a 15 yr record of DO observations from ESTOC (European Station for Time-Series in the Ocean, Canary Islands) in the eastern subtropical North Atlantic with the 20 yr record at BATS. Our estimate for net community production of oxygen was 2.3±0.4 mol O2 m−2 yr−1 and of oxygen consumption was −2.3±0.5 mol O2 m−2 yr−1 at ESTOC, and 4 mol O2 m−2 yr−1 and −4.4±1 mol m−2 yr−1 at BATS, respectively. These values were determined by analyzing the time-series using the Discrete Wavelet Transform (DWT) method. These flux values agree with similar estimates from in-situ observational studies but are higher than those from modeling studies. The difference in net oxygen production rates supports previous observations of a lower carbon export in the eastern compared to the western subtropical Atlantic. The inter-annual analysis showed clear annual cycles at BATS whereas longer cycles of nearly 4 years were apparent at ESTOC. The DWT analysis showed trends in DO anomalies dominated by long-term perturbations at a basin scale for the consumption zones at both sites, whereas yearly cycles dominated the production zone at BATS. The long-term perturbations found are likely associated with ventilation of the main thermocline, affecting the consumption and production zones at ESTOC.  相似文献   

11.
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   

12.
The fluxes of total mass, organic carbon (OC), biogenic opal, calcite (CaCO3) and long-chain C37 alkenones (ΣAlk37) were measured at three water depths (275, 455 and 930 m) in the Cariaco Basin (Venezuela) over three separate annual upwelling cycles (1996–1999) as part of the CARIACO sediment trap time-series. The strength and timing of both the primary and secondary upwelling events in the Cariaco Basin varied significantly during the study period, directly affecting the rates of primary productivity (PP) and the vertical transport of biogenic materials. OC fluxes showed a weak positive correlation (r2=0.3) with PP rates throughout the 3 years of the study. The fluxes of opal, CaCO3 and ΣAlk37 were strongly correlated (0.6<r2<0.8) with those of OC. The major exception was the lower than expected ΣAlk37 fluxes measured during periods of strong upwelling. All sediment trap fluxes were significantly attenuated with depth, consistent with marked losses during vertical transport. Annually, strong upwelling conditions, such as those observed during 1996–1997, led to elevated opal fluxes (e.g., 35 g m−2 yr−1 at 275 m) and diminished ΣAlk37 fluxes (e.g., 5 mg m−2 yr−1 at 275 m). The opposite trends were evident during the year of weakest upwelling (1998–1999), indicating that diatom and haptophyte productivity in the Cariaco Basin are inversely correlated depending on upwelling conditions.The analyses of the Cariaco Basin sediments collected via a gravity core showed that the rates of OC and opal burial (10–12 g m−2 yr−1) over the past 5500 years were generally similar to the average annual water column fluxes measured in the deeper traps (10–14 g m−2 yr−1) over the 1996–1999 study period. CaCO3 burial fluxes (30–40 g m−2 yr−1), on the other hand, were considerably higher than the fluxes measured in the deep traps (∼10 g m−2 yr−1) but comparable to those obtained from the shallowest trap (i.e. 38 g m−2 yr−1 at 275 m). In contrast, the burial rates of ΣAlk37 (0.4–1 mg m−2 yr−1) in Cariaco sediments were significantly lower than the water column fluxes measured at all depths (4–6 mg m−2 yr−1), indicating the large attenuation in the flux of these compounds at the sediment–water interface. The major trend throughout the core was the general decrease in all biogenic fluxes with depth, most likely due to post-depositional in situ degradation. The major exception was the relatively low opal fluxes (∼5 g m−2 yr−1) and elevated ΣAlk37 fluxes (∼2 mg m−2 yr−1) measured in the sedimentary interval corresponding to 1600–2000 yr BP. Such compositions are consistent with a period of low diatom and high haptophyte productivity, which based on the trends observed from the sediment traps, is indicative of low upwelling conditions relative to the modern day.  相似文献   

13.
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   

14.
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   

15.
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   

16.
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   

17.
Particulate organic carbon (POC) concentrations from 0 to 1000 m were quantified in size-fractionated particulate matter samples obtained by the multiple unit large volume in situ filtration system (MULVFS) in 1996 and 1997 along the 1600 km long “line P” transect from continental slope waters near southern Vancouver Island to Ocean Station PAPA (OSP, 50°N, 145°W). Regression of in situ POC vs. beam attenuation coefficient, c, from a simultaneously deployed 1-m pathlength SeaTech transmissometer gave slope, intercept and r2 values of 6.15±0.19×10−5 m−1 (nmol C l−1)−1, 0.363±0.003 m−1, and 0.951 (n=145), respectively. This result agreed within several percent of calibrations obtained from two 2600-km-long transects of the equatorial Pacific in 1992 (Bishop, 1999). Data from other, more frequently deployed transmissometers were standardized against the 1-m instrument, and the combined optical data set was used to document POC variability at finer spatial and temporal scales than could be sampled directly using either conventional water bottle casts or MULVFS. Published bottle POC vs. c relationships show much more variability and remain problematic. Along the line P transect in the salinity-stratified upper 100 m, POC isolines shoaled from winter to summer in concert with seasonal stratification. At the same time, POC was progressively enriched in subeuphotic zone waters to depths greater than 500 m. Near-surface POC fields sampled in the winter time showed strong temporal POC variability over time scales of days as well as between years. POC concentrations at OSP in February 1996 were higher than those found at any other time of year. Less variability was found along line P in other seasons. In May 1996, kilometer-scale spatial variability of POC at OSP was small; dawn vs. dusk variations of c were used to calculate 0–100 m POC turnover times shorter than 6 d. Calculations also suggest that 25–50% of primary productivity was expressed as dissolved organic carbon at OSP in May 1996.  相似文献   

18.
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   

19.
Satellite remote sensing offers new means of quantifying particulate organic carbon, POC, concentration over large oceanic areas. From SeaWiFS ocean color, we derived 10-year data of POC concentration in the surface waters of the global ocean. The 10-year time series of the global and basin scale average surface POC concentration do not display any significant long-term trends. The annual mean surface POC concentration and its seasonal amplitude are highest in the North Atlantic and lowest in the South Pacific, when compared to other ocean basins. POC anomalies in the North Atlantic, North Pacific, and global concentrations seem to be inversely correlated with El Niño index, but longer time series are needed to confirm this relationship. Quantitative estimates of POC reservoir in the oceanic surface layer depend on the choice of what should represent this layer. Global average POC biomass is 1.34 g m?2 if integrated over one optical depth, 3.62 g m?2 if integrated over mixed layer depth, and up to 6.41 g m?2 if integrated over 200-m layer depth (when assumed POC concentration below MLD is 20 mg m?3). The global estimate of total POC reservoir in the surface 200-m layer of the ocean is 228.61×1013 g. We expect that future estimates of POC reservoir may be even larger, when more precise calculations account for deep-water organic-matter maxima in oligotrophic regions, and POC biomass located just below the seasonal mixed layer in spring and summer in the temperate regions.  相似文献   

20.
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   

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