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1.
Measurements of gas-, particle- and precipitation-phases of atmospheric mercury (Hg) were made in the South and equatorial Atlantic Ocean as part of the 1996 IOC Trace Metal Baseline Study (Montevideo, Uruguay to Barbados). Total gaseous mercury (TGM) ranged from 1.17 to 1.99 ng m−3, with a weighted mean of 1.61±0.09 ng m−3. These values compare well with Pacific Ocean data and earlier results from the Atlantic. The open-ocean samples recorded a distinctive inter-hemispheric gradient, which is consistent with a long-lived trace gas emitted to a greater extent from the Northern than from the Southern Hemisphere. Correlations with surface 222Rn measurements indicate an influence of regional terrestrial sources on open-ocean TGM concentrations. Total Hg in precipitation ranged from 10 to 99 pM (volume-weighted average: 17.8±2.9 pM). On average, about 72% of the total Hg was “reactive” (i.e., reducible by SnCl2). The data showed an apparent rapid nonlinear decrease in concentration with event size (“washout curve”). The wet depositional flux was estimated at 18–36 nmol m−2 yr−1 (4–7 μg m−2 yr−1), which is slightly lower than that found in mid-continental locations of North America (6–12 μg m−2 yr−1). 210Pb analyses indicate a strong impact of particles on rain Hg concentrations. Particle-phase Hg (range 5–25 fmol m−3; mean 12±1 fmol m−3; 66% “reactive”) was comparable to values over the equatorial Pacific. The dry depositional flux is ca. 0.4 nmol m−2 yr−1, or 0.4–1.0% of the wet flux. Particle-phase Hg concentrations did not change significantly when African dust was present during sampling. However, the Hg/Al ratios were consistent with crustal values during the dust periods. The residence time of TGM was calculated to be 1.3–3.4 yr in this region, based on standing stock estimates. Incubation of rainwater added to surface seawater gave reduction rates [i.e., production of elemental Hg (Hg°); 1.6–4.3% d of total Hg added] comparable to additions of inorganic ionic standards, indicating that Hg+2 from precipitation is reduced in a similar manner in surface waters. Thus, precipitation-phase Hg is generally available for evasion to the atmosphere following deposition to the surface ocean, effectively enhancing the mobility and residence time of Hg at the Earth's surface.  相似文献   

2.
A 2-yr record of downward particle flux was obtained with moored sediment traps at several depths of the water column in two regions characterized by different primary production levels (mesotrophic and oligotrophic) of the eastern subtropical North Atlantic Ocean. Particle fluxes, of ∼71–78% biogenic origin (i.e. consisting of CaCO3, organic matter and opal) on average, decrease about six-fold from the mesotrophic site (highest fluxes in the North Atlantic) nearer the Mauritanian margin (18°30′N, 21°00′W) to the remote, open-ocean, oligotrophic site (21°00′N, 31°00′W). This decrease largely reflects the difference in total primary production between the two sites, from ∼260 to ∼110 g organic C m−2 yr−1. At both sites, temporal variability of the downward particle flux seems to be linked to westward surface currents, which are likely to transport seaward biomass-rich water masses from regions nearer the coast. The influence of coastal upwelling is marked at the mesotrophic site. The large differences between the 1991 and 1992 records at that site, where carbon export is large, underscore the interest of long-term studies for export budget estimates. The different productivity regimes at the two sites seem to induce contrasting downward modes of transport of the particulate matter, as shown in particular by the faster settling rates and the higher E ratio (particulate organic carbon export versus total primary production) estimated at the mesotrophic site.  相似文献   

3.
In order to characterize our study area and to provide reference values to be used in the future to measure the changes produced by an increase in contamination, the concentrations of chlorinated hydrocarbons have been investigated in fifty-one samples of seawater, taken at four different depths: air-sea interface, surface, one metre and bottom waters, and in twenty-three samples of surface sediments from Blanca Bay, Argentina. Of eleven organochlorine compounds we were looking for (α BHC, lindane, heptachlor, δ BHC. aldrin, heptachlor epoxide, dieldrin, o-p′DDD, p-p′DDD, o-p′DDT and p-p′DDT), seven could be detected in seawater and three in surface sediments with the following mean concentrations: α-BHC=48·2 ng l?1; lindane=54·2 ng l?1; heptachlor=45·0 ng l?1; δ BHC=12·5 ng l?1; aldrin=61·8 ng l?1 and ΣDDT=67·0 ng l?1; and δ BHC=3·2 ng g?1; lindane=4·2 ng g?1 and heptachlor=1·0 ng g?1 for seawater, regarding the surface waters, and sediment samples, respectively.Concentration factors among the different water layers were also studied to see if there was any correlation between chlorinated hydrocarbon contents and the water depths from which the samples were taken. As a mean value, the air-sea interface water contains 18 times more of these compounds than that of the water near the bottom. A comparison of the values corresponding to seawater and surface sediments from our study area with those levels measured in samples from other geographic locations is also presented.With the purpose to detect a relationship between chlorinated hydrocarbon concentrations and the contents of particulate matter (PM) on the one hand, and particulate organic material (POM) on the other hand, four groups of samples containing different amounts of PM and POM, respectively were formed. From a comparison of the results obtained, lindane, heptachlor and δ BHC showed a tendency to lower concentrations in those samples containing little PM whereas α BHC and aldrin remained without important changes. No significant correlation was found between organochlorine levels and contents of POM.  相似文献   

4.
Nitrogen uptake rates, and physical, chemical and biological characteristics of the euphotic zone were studied in winter, spring and late summer during the period 1992–1994 along a transect (Line P) extending from the continental slope off the southwest corner of Vancouver Island (British Columbia, Canada; station P4; 49°N, 127°W) to open waters in the NE Pacific (OSP; 50°N, 145°W). Nitrate (NO3−) and silicic acid (Si(OH)4) concentrations increased offshore during every season. Lowest NO3− and Si(OH)4 values were observed during late summer and spring, and highest during winter throughout the euphotic zone. For spring and late summer, surface depletion of NO3− was observed at the inshore end of the transect, while offshore concentrations were never limiting for phytoplankton growth. Silicic acid was never depleted at any depth or station during the period covered by this study. Ammonium (NH4+) and urea concentrations exhibited a patchy distribution along the transect, with no seasonal variations. Chlorophyll a and particulate nitrogen did not show a consistent longitudinal pattern from year to year. In general, the highest concentrations of chlorophyll a and particulate nitrogen were measured during the late summer cruises, with lower values in spring and lowest in winter. Phytoplankton assemblages were numerically dominated by flagellates <5 μm throughout the water column on each cruise transect. Ammonium, urea and NO3− uptake rates represented on average 55, 24 and 21% of the depth-integrated total nitrogen uptake, both longitudinally and seasonally; hence, phytoplankton utilized nitrogen in the following order: NH4+>urea>NO3− along Line P. Ammonium may have inhibited the uptake rates of NO3− and urea. Urea uptake rates were lower than those of NH4+, but higher values were occasionally observed at a few depths along the transect, particularly during the spring of 1993. Depth-integrated NH4+ uptake rates were generally higher inshore, while NO3− uptake rates showed higher values offshore during most seasons. In contrast, urea uptake rates did not exhibit a consistent longitudinal trend. The depth-integrated f-ratio ranged from 0.05 to 0.37 with an average of 0.21 for all stations and cruises, and was overestimated on average by 36% when urea was excluded from the calculation. On a yearly basis, primary productivity in the NE subarctic Pacific was based on regenerated nitrogen.  相似文献   

5.
A total of 150 samples were collected at a 10-days' anchor station in the Bornholm basin (55° 31.1′N, 15° 32.1′E) and analyzed for dissolved (< 0.4 μm) and particulate trace metals. For dissolved Mn, large gradients have been found in the vertical distribution with minimum concentrations (< 0.2 μgl?1) in the halocline zone and considerably higher values in the deep waters (up to 50 μgl?1). Ultrafiltration studies indicate that dissolved Mn is probably present as Mn2+ in the oxygenated bottom layer. The primary production process was not evident in the particulate Mn profile; the suspended particulate material (SPM), however, shows a considerable enrichment with depth, apparently due to Mn-oxide precipitation.The distribution of dissolved Fe was rather homogeneous, with average concentrations throughout the water column between 0.86 and 1.1 μgl?1, indicating that the oxidation of Fe2+ ions released from the sediments must already be complete in the very near oxidation boundary layer. Relatively high concentrations of particulate Fe were actually measured in the bottom layer, with the maximum mean of 11.2 μgl?1 at 72 m. Similarly to Mn, the profile of particulate Fe does not reflect the SPM curve of the eutrophic layer. On average, about 70% of the total Fe in surface waters was found to be particulate.The average concentrations of dissolved Zn, Cd and Cu were found to be rather homogeneous in the water column but showed a relatively high variability with time. A simplified model on trace-metal uptake by phytoplankton indicates no significant change in dissolved metal concentrations during the period of investigation. On average, only 1.7% Zn, 3.3% Cd and 9.8% Cu of the total metal concentrations were found in particulate form. SPM analyses showed significant correlations of Zn, Cd and Cu with Fe, indicating that particulate iron is an important carrier for particulate trace metals in Baltic waters.  相似文献   

6.
《Oceanologica Acta》1998,21(4):533-542
Seawater samples collected in the northeast Pacific from 112° 50′W to 126° 36′W along a latitudinal band (21–25° N) have been analysed for 228RA and 226Ra. Both nuclides exhibit their characteristic distributions. In the surface water, the exponential-like decrease of 228 Ra away from Baja California can be interpreted by horizontal water mixing with eddy diffusion coefficients (Kx) of 1 × 106 cm2 s−1 and 5 × 107 cm2 S−1 for scale lengths of 200 km and 1000 km, respectively. In the bottom waters, the decrease of 228Ra away from bottom sediments can be modeled by vertical eddy diffusivities (Kz) of 15–30 cm2 s−1 except at one station (24° 16.9′ N, 115° 8.9′ W) where a value of 120 cm2 s−1 is obtained. The 228Ra-derived diffusivities were used to compute the mass balance of 226Ra using a two-box model. The model results show a mean mixing coefficient of 3.8 cm2 s−1 for the thermocline and a mean upwelling velocity of 7.7 m y−1 in the study area, both are about two or three times higher than those generally quoted for the Pacific.  相似文献   

7.
Decomposition experiments were conducted on cultured phytoplankton (Skeletonema costatum) in seawater containing decomposer and consumer of size less than 500 μm. We determined the decomposition rates of bulk particulate organic matter (POM), the ratio of labile to semi-refractory fractions in the POM, and the POM carbon/ nitrogen (C/N) ratio during decomposition. To identify the kinetic mechanisms involved in the reactions of different order (e.g., first- and second-order), we studied the sensitivity of reaction rates to the initial concentration of POM, ranging from 2.4 to 71 mg-C L−1. The results showed that decomposition consists of two first-order reactions: decomposition of labile and of semi-refractory particulate organic carbon (POC). The decomposition rate constants found for labile (0.13 day−1 at 20°C), and semi-refractory POC (0.008 day−1 at 20°C), and the carbon weight ratio of semi-refractory POC (13% at 20°C), were insensitive to the initial organic matter concentration. The time-dependence of the C/N ratio was also independent of this initial concentration. The decomposition rate constants and the content of semi-refractory POC did not change, regardless of the absence or presence of 25–500 μm organisms in natural seawater. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

8.
A modified version of the Coomassie Brilliant Blue dye binding protein assay has been developed for oceanographic samples and intercalibrated with the widely used Lowry assay. Particulate protein measurements were made at seven stations in the Gulf of Maine using the method. Measurements were made on cell-free homogenates. Protein concentration ranged from 2 to 212 μg l?1 (0.02–0.68 μg at N l?1) and averaged 58 μg l?1. ETS activity, chlorophyll and particulate nitrogen were significantly correlated with protein concentrations.  相似文献   

9.
We analyzed the stable nitrogen isotope composition of an extensive set of samples of particulate matter (PM) and seawater nitrate collected during October/November 1997 along the Mexican coastline from 24° to 11.5°N. At the northern and southern end of our study area, the δ15N of PM ranged between 5 and 7‰ in the upper 200 m of the water column with higher values at intermediate depths. These data are very similar to those reported from other parts of the open ocean. In the oxygen minimum zone (OMZ), we found significantly higher δ15N values for suspended particles. Furthermore, the δ15N of nitrate (NO3) was elevated within the OMZ and we found a strong relationship between the oxygen concentration, nitrate deficit and the 15N content of the nitrate. The core of the OMZ between 22°N, 105°W and 15°N, 110°W coincided with higher nitrate deficits and δ15N values relative to the stations near the boundaries. The δ15N of nitrate was highest, with values up to 18.7‰, where oxygen concentrations were below 1–2 μmol/l. This pattern is consistent with an overall nitrogen isotopic enrichment factor of 22.5‰ for denitrification in the core of the OMZ using the Rayleigh equation (closed-system approach). Results from a diffusion model (open-system approach), however, gave a fractionation factor of 30±7.5‰, implying that the Rayleigh formula only gives a lower estimate of the fractionation factor ε. The vertical flux of particles collected in short-term deployments (ca. 35 h) of a drifting sediment trap was not significantly correlated with the water column nitrate deficit. The isotopic signature of the nitrate within the gradient is very similar to the δ15N value of sedimenting particles, suggesting that there might be a strong link between the production and sedimentation of particles. Upward flux of nitrate across the thermocline can account for less than half of the particle flux leaving the mixed layer. Mixing and transport of nitrate across the lower boundary of the OMZ can lead to significant enrichment in the 15N content of deep waters, and our isotopic data imply that at least 14% of the nitrate in the waters below the OMZ originates from this source.  相似文献   

10.
Dissolved and labile particulate Zr, Hf, Nb, Ta, Mo and W were determined at stations K1 (51°N, 165°E), K2 (47°N, 160°E), KNOT (44°N, 155°E) and 35N (35°N, 160°E) in the western North Pacific Ocean. A portion of seawater for dissolved species (D) was passed through a 0.2 μm Nuclepore filter and acidified to pH 2.2 with HCl and HF. A portion of seawater for acid-dissolvable species (AD) was acidified without filtration. Labile particulate (LP) species is defined as AD minus D, which represents a chemically labile fraction of particulate species. D-Zr, Hf and Ta increase with depth, Nb shows a slight depletion in surface water, whereas Mo and W have a conservative vertical profile. The concentration range of D-Zr, Hf, Nb, Ta and W is 31–275, 0.14–0.95, 4.0–7.2, 0.08–0.29 and 40–51 pmol kg−1, respectively, whereas that of Mo is 97–105 nmol kg−1. LP-species of Zr, Hf and Ta account for 10–14% of AD in average and increase up to 25% below 4000 m, whereas those for Mo and W are negligible. In contrast, LP-Nb shows maxima (up to 27%) in surface water. We also found that D-Zr/Hf, Nb/Ta and Mo/W mole ratios generally increase in the order continental crust < river water < coastal sea < open ocean.  相似文献   

11.
The concentrations of suspended matter and particulate Cd, Cu, Pb and Zn were determined for 36 samples collected at 6 stations in the Antarctic Ocean during December, 1970 and January, 1971 using membrane filters. The concentration of suspended matter was determined gravimetrically and trace metal levels were determined using anodic stripping voltammetry. For waters deeper than 100 m the concentration of suspended matter was < 100 μg l?1. Concentrations up to 542 μg l?1 were recorded between surface and 100 m. Individual concentrations of the metals were scattered with depth. Average concentrations of particulate metals were: Cd, 3.5 ng l?1; Cu, 100 ng l?1; Pb, 35 ng l?1; and Zn, 230 ng ;l?1 These measurements represent non-steady state conditions of early Antarctic summer as the ice pack disintegrates and biological activity increases.  相似文献   

12.
《Marine Chemistry》2002,80(1):11-26
Profiles of particulate and dissolved 234Th (t1/2=24.1 days) in seawater and particulate 234Th collected in drifting traps were analyzed in the Barents Sea at five stations during the ALV3 cruise (from June 28 to July 12, 1999) along a transect from 78°15′N–34°09′E to 73°49′N–31°43′E. 234Th/238U disequilibrium was observed at all locations. 234Th data measured in suspended and trapped particles were used to calibrate the catchment efficiency of the sediment traps. Model-derived 234Th fluxes were similar to 234Th fluxes measured in sediment traps based on a steady-state 234Th model. This suggests that the sediment traps were not subject to large trapping efficiency problems (collection efficiency ranges from 70% to 100% for four traps). The export flux of particulate organic carbon (POC) can be calculated from the model-derived export flux of 234Th and the POC/234Th ratio. POC/234Th ratios measured in suspended and trapped particles were very different (52.0±9.9 and 5.3±2.2 μmol dpm−1, respectively). The agreement between calculated and measured POC fluxes when the POC/234Th ratio of trapped particles was used confirms that the POC/234Th ratio in trap particles is representative of sinking particles. Large discrepancies were observed between calculated and measured POC fluxes when the POC/234Th ratio of suspended particles was used. In the Barents Sea, vertical POC fluxes are higher than POC fluxes estimated in the central Arctic Ocean and the Beaufort Sea and lower than those calculated in the Northeast Water Polynya and the Chukchi Sea. We suggest that the latter fluxes may have been strongly overestimated, because they were based on high POC/234Th ratios measured on suspended particles. It seems that POC fluxes cannot be reliably derived from thorium budgets without measuring the POC/234Th ratio of sediment trap material or of large filtered particles.  相似文献   

13.
《Marine Chemistry》2006,98(2-4):210-222
This study presents concentrations of dimethylsulphide (DMS) and its precursor compound dimethylsulphoniopropionate (DMSP) in a variety of sea ice and seawater habitats in the Antarctic Sea Ice Zone (ASIZ) during spring and summer. Sixty-two sea ice cores of pack and fast ice were collected from twenty-seven sites across an area of the eastern ASIZ (64°E to 110°E; and the Antarctic coastline north to 62°S). Concentrations of DMS in 81 sections of sea ice ranged from < 0.3 to 75 nM, with an average of 12 nM. DMSP in 60 whole sea ice cores ranged from 25 to 796 nM and showed a negative relationship with ice thickness (y = 125x− 0.8). Extremely high DMSP concentrations were found in 2 cores of rafted sea ice (2910 and 1110 nM). The relationship of DMSP with ice thickness (excluding rafted ice) suggests that the release of large amounts of DMSP during sea ice melting may occur in discrete areas defined by ice thickness distribution, and may produce ‘hot spots’ of elevated seawater DMS concentration of the order of 100 nM. During early summer across a 500 km transect through melting pack ice, elevated DMS concentrations (range 21–37 nM, mean 31 nM, n = 15) were found in surface seawater. This band of elevated DMS concentration appeared to have been associated with the release of sea ice DMS and DMSP rather than in situ production by an ice edge algal bloom, as chlorophyll a concentrations were relatively low (0.09–0.42 μg l− 1). During fast ice melting in the area of Davis station, Prydz Bay, sea ice DMSP was released mostly as extracellular DMSP, since intracellular DMSP was negligible in both hyposaline brine (5 ppt) and in a melt water lens (4–5 ppt), while extracellular DMSP concentrations were as high as 149 and 54 nM, respectively in these habitats. DMS in a melt water lens was relatively high at 11 nM. During the ice-free summer in the coastal Davis area, DMS concentrations in surface seawater were highest immediately following breakout of the fast ice cover in late December (range 5–14 nM), and then remained at relatively low concentrations through to late February (< 0.3–6 nM). These measurements support the view that the melting of Antarctic sea ice produces elevated seawater DMS due to release of sea ice DMS and DMSP.  相似文献   

14.
The concentration of dimethylsulfide (DMS) and supporting parameters were determined in surface seawater and vertical profiles at 26 stations in the South China Sea. The concentrations of DMS in surface seawater ranged from 61 to 148 ng S/l, with a mean of 82 ng S/l. High concentrations of DMS were found in the productive regions. The vertical profiles of DMS were characterized by a maximum at depths typically between 20 and 75 m. The concentrations of DMS were correlated with the levels of chlorophyll a both in the surface seawater and in the vertical distribution. The concentrations of DMS were higher than expected for this chlorophyll-poor tropical sea, as indicated by markedly high DMS (ng S/l)/chlorophyll a (μg/l) ratios ranging from 315 to 3524 with a mean of 1768 for all the surface seawater samples. DMS concentration was significantly correlated with seawater temperature and dissolved oxygen, but it showed an inverse relationship to nutrients (including nitrate, phosphate and silicate). On the basis of sea surface concentrations of DMS and gas exchange calculations, the mean flux of DMS from the South China Sea to the atmosphere was estimated to be 5.5 μmol m−2 d−1.  相似文献   

15.
九龙江河口区稀土元素地球化学特征   总被引：1，自引：0，他引：1  
用电感耦合等离子体质谱（ICP-MS）对2007年10月航次采集的九龙江河口区溶解态、悬浮颗粒态、沉积物样品中的稀土元素（REEs）进行了测定,对REEs的地球化学特征进行研究.结果表明,REEs在各相态中的含量范围如下：溶解态的为0.1 ng/dm^3（Eu）～1.96μg/dm^3（Ce）,悬浮颗粒态的为0.28（Tm）～142.83（Ce）mg/kg,沉积物的为0.25（Tm）～99.65（Ce）mg/kg;溶解态、悬浮颗粒态及沉积物中REEs球粒陨石标准化配分曲线均表现为负斜率型,九龙江河口为LREE相对HREE富集型河口.九龙江河口溶解态、悬浮颗粒态、沉积物三相态中REEs含量受流域土壤、地表径流等源区因素影响较大.Ce异常值在各相态中表现为负异常.  相似文献   

16.
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   

17.
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   

18.
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   

19.
The abundance of tintinnid ciliates in lower Narragansett Bay was measured at weekly intervals over the period 1980–1982. Twenty-nine species representing nine genera ranged in abundance from 101 to 105 tintinnids l−1. Tintinnopsis was the most numerous genus in terms of numbers of species and individuals. Total abundance increased with water temperature above 6°C, and with nanoplankton chlorophyll a (<10 μm and <5 μm chl a) averaged over the water column. Exceptions occurred during blooms of phytoplankton previously demonstrated to be poor food for tintinnids (Olisthodiscus, Thalassiosira). Tintinnids aggregated near the bottom during periods of low nanoplankton chl a. Abundances and distributions were not correlated with particulate organic carbon. Seasonal changes in length and oral diameter of loricas of individual species were inversely related to temperature. Oral diameter was a more constant feature of lorica morphology than length. Seasonal patterns in the mean oral diameter of the lorica of all species reflected decreases in the oral diameter of individual species with increasing temperature, and changes from small to large species coincident with similar shifts in the size of phytoplankton. The production rate of tintinnids was 3·3 mgCl−1 year−1, equivalent to the ingestion of 26% of total annual net primary production and 52% of the estimated production of <10 μm phytoplankton.  相似文献   

20.
Seventy percent of 342 seawater samples collected in the Bering Sea, North and South Pacific, Japan Sea, East and South China Seas, and Indian Ocean had concentrations of “total” mercury ranging from 3 to 6 ng Hg l?1 with an arithmetic mean of 5.3 ng l?1 and a geometric mean of 5.0 ng l?1. In some cases, a higher concentration was observed at the surface, at the halocline or thermocline, or in the bottom water. But in general, there was no consistent correlation between mercury concentration and depth, except for a statistical tendency for mercury concentration to be slightly higher in the surface water. This tendency suggests that mercury in the ocean is supplied from the atmosphere by rain washout. The latitudinal variation of surface mercury concentrations showed that the maximum concentration at each latitude decreased from 40°N to 30°S. This variation provides evidence that atmospheric mercury is emitted mainly from continental areas naturally or anthropogenically.  相似文献   

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