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1.
Within the framework of the EU-funded BENGAL programme, the effects of seasonality on biogenic silica early diagenesis have been studied at the Porcupine Abyssal Plain (PAP), an abyssal locality located in the northeast Atlantic Ocean. Nine cruises were carried out between August 1996 and August 1998. Silicic acid (DSi) increased downward from 46.2 to 213 μM (mean of 27 profiles). Biogenic silica (BSi) decreased from ca. 2% near the sediment–water interface to <1% at depth. Benthic silicic acid fluxes as measured from benthic chambers were close to those estimated from non-linear DSi porewater gradients. Some 90% of the dissolution occurred within the top 5.5 cm of the sediment column, rather than at the sediment–water interface and the annual DSi efflux was close to 0.057 mol Si m−2 yr−1. Biogenic silica accumulation was close to 0.008 mol Si m−2 yr−1 and the annual opal delivery reconstructed from sedimentary fluxes, assuming steady state, was 0.065 mol Si m−2 yr−1. This is in good agreement with the mean annual opal flux determined from sediment trap samples, averaged over the last decade (0.062 mol Si m−2 yr−1). Thus ca. 12% of the opal flux delivered to the seafloor get preserved in the sediments. A simple comparison between the sedimentation rate and the dissolution rate in the uppermost 5.5 cm of the sediment column suggests that there should be no accumulation of opal in PAP sediments. However, by combining the BENGAL high sampling frequency with our experimental results on BSi dissolution, we conclude that non-steady state processes associated with the seasonal deposition of fresh biogenic particles may well play a fundamental role in the preservation of BSi in these sediments. This comes about though the way seasonal variability affects the quality of the biogenic matter reaching the seafloor. Hence it influences the intrinsic dissolution properties of the opal at the seafloor and also the part played by non-local mixing events by ensuring the rapid transport of BSi particles deep into the sediment to where saturation is reached.  相似文献   

2.
Mesoscale eddies may enhance primary production (PP) in the open ocean by bringing nutrient-rich deep waters into the euphotic zone, potentially leading to increased transport of particles to depth. This hypothesis remains controversial, however, due to a paucity of direct particle export measurements. In this study, we investigated particle dynamics using 234Th–238U disequilibria within a mesoscale cold-core eddy, Cyclone Opal, which formed in the lee of the Hawaiian Islands. 234Th samples were collected along two transects across Cyclone Opal as well as during a time-series within the eddy core during a decaying diatom bloom. Particulate carbon (PC), particulate nitrogen (PN) and biogenic silica (bSiO2) fluxes at 150 m varied spatially and temporally within the eddy and strongly depended on the 234Th model formulation used (e.g., steady state versus non-steady state, inclusion of upwelling, etc.). Particle fluxes estimated from a steady state model assuming an upwelling rate of 2 m day−1 yielded the best fit to sediment-trap data. These 234Th-derived particle fluxes ranged from 332±14 to 1719±53 μmol C m−2 day−1, 27±3 to 114±12 μmol N m−2 day−1, and 33±20 to 309±73 μmol Si m−2 day−1. Although PP rates within Cyclone Opal were elevated by a factor of 2–3, PC and PN fluxes were the same, within error, inside and outside of Cyclone Opal. The ratio of PC export to PP remained surprisingly low at <0.03 and similar to those measured in surrounding waters. In contrast, bSiO2 fluxes within the eddy core were three times higher. Detailed analyses of 234Th depth profiles consistently showed excess 234Th at 100–175 m, associated with the remineralization and possible accumulation of suspended and dissolved organic matter from the surface. We suggest that strong microzooplankton grazing facilitated particulate organic matter recycling and resulted in the export of empty diatom frustules. Thus, while eddies may increase PP, they do not necessarily increase PC and PN export to deep waters. This may be a general characteristic of wind-driven cyclonic eddies of the North Pacific Subtropical Gyre and suggests that eddies may preferentially act as a silica pump, thereby playing an important role in promoting silicic-acid limitation in the region.  相似文献   

3.
The study on dissolved organic ligands capable to complex copper ions (LT), surface-active substances (SAS) and dissolved organic carbon (DOC) in the Northern Adriatic Sea station (ST 101) under the influence of Po River was conducted in period from 2006–2008. The acidity of surface-active organic material (Acr) was followed as well. The results are compared to temperature and salinity distributions. On that way, the contribution of the different pools of ligands capable to complex Cu ions could be determined as well as the influence of aging and transformation of the organic matter. The LT values in the investigated period were in the range of 40–300 nmol l−1. The range of DOC values for surface and bottom samples were 0.84–1.87 mg l−1 and 0.80–1.30 mg l−1, respectively. Total SAS concentrations in the bottom layer were 0.045–0.098 mg l−1 in equiv. of Triton-X-100 while those in the surface layer were 0.050–0.143 mg l−1 in equiv. of Triton-X-100. The majority of organic ligands responsible for Cu binding in surface water originate from new phytoplankton production promoted by river borne nutrients. Older, transformed organic matter, possessing higher relative acidity, is the main contributor to the pool of organic ligands that bind copper in the bottom samples. It was estimated that 9% of DOC in surface samples and 12% of DOC in the bottom samples are present as ligands capable to complex copper ions.  相似文献   

4.
A coupled physical–biological model was developed to simulate the low-silicate, high-nitrate, and low-chlorophyll (LSHNLC) conditions in the equatorial Pacific Ocean and used to compute a detailed budget in the Wyrtki box (5°N–5°S, 180–90°W) for the major sources and cycling of nitrogen and silicon in the equatorial Pacific. With the incorporation of biogenic silicon dissolution, NH4 regeneration from organic nitrogen and nitrification of ammonia in the model, we show that silicon recycling in the upper ocean is less efficient than nitrogen. As the major source of nutrients to the equatorial Pacific, the Equatorial Undercurrent provides slightly less Si(OH)4 than NO3 to the upwelling zone, which is defined as 2.5°N–2.5°S. As a result, the equatorial upwelling supplies less Si(OH)4 than NO3 into the euphotic zone in the Wyrtki box, having a Si/N supply ratio of about 0.85 (2.5 vs. 2.96 mmolm−2 day−1). More Si(OH)4 than NO3 is taken up with a Si/N ratio of 1.17 (2.72 vs. 2.33 mmolm−2 day−1) within the euphotic zone. The difference between upwelling supply and biological uptake is balanced by nutrient regeneration and horizontal advection. Excluding regeneration, the net silicate and nitrate uptakes are nearly equal (1.76 vs. 1.84 mmolm−2 day−1). However, biogenic silica export production is slightly higher than organic nitrogen (1.74 vs. 1.59 mmolm−2 day−1) following a 1.1 Si/N ratio. In the central equatorial Pacific, low silicate concentrations limit diatom growth; therefore non-diatom new production accounts for most of the new production. Higher silicate supply in the east maintains elevated diatom growth rates and new production associated with diatoms dominate upwelling zone. In contrast, the new production associated with small phytoplankton is nearly constant or decreases eastward along the equator. The total new production has a higher rate in the east than in the west, following the pattern of surface silicate. This suggests that silicate regulates the diatom production, total new production, and thereby carbon cycle in this area. The modeled mean primary production is 48.4 mmolCm−2 day−1, representing the lower end of direct field measurements, while new production is 15.0 mmolCm−2 day−1, which compares well with previous estimates.  相似文献   

5.
An intense diatom bloom developed within a strong meridional silicic acid gradient across the Antarctic Polar Front at 61°S, 170°W following stratification of the water column in late October/early November 1997. The region of high diatom biomass and the silicic acid gradient propogated southward across the Seasonal Ice Zone through time, with the maximum diatom biomass tracking the center of the silicic acid gradient. High diatom biomass and high rates of silica production persisted within the silicic acid gradient until the end of January 1998 (ca. 70 d) driving the gradient over 500 km to the south of its original position at the Polar Front. The bloom consumed 30 to >40 μM Si(OH)4 in the euphotic zone between about 60 and 66°S leaving near surface concentrations <2.5 μM and occasionally <1.0 μM in its wake. Integrated biogenic silica concentrations within the bloom averaged 410 mmol Si m−2 (range 162–793 mmol Si m−2). Average integrated silica production on two consecutive cruises in December 1997 and January 1998 that sampled the bloom while it was well developed were 27.5±6.9 and 22.6±20 mmol Si m−2 d−1, respectively. Those levels of siliceous biomass and silica production are similar in magnitude to those reported for ice-edge diatom blooms in the Ross Sea, Antarctica, which is considered to be among the most productive regions in the Southern Ocean. Net silica production (production minus dissolution) in surface waters during the bloom was 16–21 mmol Si m−2 d−1, which is sufficient for diatom growth to be the cause of the southward displacement of the silicic acid gradient. A strong seasonal change in silica dissolution : silica production rate ratios was observed. Integrated silica dissolution rates in the upper 100–150 m during the low biomass period before stratification averaged 64% of integrated production. During the bloom integrated dissolution rates averaged only 23% of integrated silica production, making 77% of the opal produced available for export to depth. The bloom ended in late January apparently due to a mixing event. Dissolution : production rate ratios increased to an average of 0.67 during that period indicating a return to a predominantly regenerative system.Our observations indicate that high diatom biomass and high silica production rates previously observed in the marginal seas around Antarctica also occur in the deep ocean near the Polar Front. The bloom we observed propagated across the latitudinal band overlying the sedimentary opal belt which encircles most of Antarctica implying a role for such blooms in the formation of those sediments. Comparison of our surface silica production rates with new estimates of opal accumulation rates in the abyssal sediments of the Southern Ocean, which have been corrected for sediment focusing, indicate a burial efficiency of 4.6% for biogenic silica. That efficiency is considerably lower than previous estimates for the Southern Ocean.  相似文献   

6.
During the EPOS leg 2 cruise (European Polarstern Study, November 1988–January 1989), the production rate of biogenic silica in the euphotic zone was measured by the 30Si method at stations in the Scotia and Weddell Seas.The highest integrated production rates were observed in the Scotia Sea (range: 11.2–20.6 mmol Si m−2 day−1), the marginal ice zone of the Weddell Sea exhibiting somewhat lower values (range: 6.0–20.0 mmol Si m−2day−1).Our results demonstrate that as far as biogenic silica production is concerned the marginal ice zone of the Weddell Sea is considerably less productive than that of the Ross Sea. Our results also indicate that the water of the Antarctic Circumpolar Current (ACC) could be more productive in late spring and early summer than at the beginning of spring. Possible reasons for the differences among the three subsystems (Ross Sea, Weddell Sea and ACC) are discussed.  相似文献   

7.
Samples of lake water and coastal seawater from Nova Scotia, Canada, were irradiated with natural or artificial sunlight to investigate the potential for photochemical hydrogen production. Hydrogen photo-production was observed in all natural water samples. Rates of hydrogen formation were highest in coloured lake water (range: 98–163 pmol L− 1h− 1) and lower in seawater (range: 19–45 pmol L− 1 h − 1). Dilutions of the most highly coloured lake sample (Kejimkujik Lake) showed a positive linear relationship between H2 production rates and CDOM concentration. Photo-production rates normalised to UV absorption coefficients at 350 nm indicated that the photochemical efficiency of hydrogen formation varied between samples, perhaps due to differences in the CDOM composition. Photochemical hydrogen formation was also seen in solutions of syringic acid and acetaldehyde: two low-molecular-weight carbonyl compounds found in natural waters. Photochemistry may therefore offer least a partial explanation for the persistently high levels of hydrogen observed in the low-latitude surface ocean.  相似文献   

8.
In this study, the contents, sources and accumulation rate of sedimentary organic matter (OM) in the Pearl River Estuary (PRE) and adjacent coastal area were investigated. The stable carbon isotopic composition (δ13C) is a reliable geochemical proxy and was used to indicate the OM origin here. Nevertheless, the organic carbon and nitrogen molar ratios (TOC/TN) and the stable nitrogen isotopic composition (δ15N) were affected by diagenesis and could be the supplementary indicators. The sources of OM were estimated based on the two end-member model. The results showed that in the estuary, sedimentary OM originated from terrestrial and aquatic mixing origins, whereas, OM in coastal sediments was dominantly algae-derived. The accumulation rate of sedimentary OM was analyzed based on 210Pb dating. Due to the sampling sites and the distinct hydraulic environments, the accumulation rates of TOC, aquatic and terrestrial OC were obviously higher in the estuary than in coastal area. TOC accumulation rates were 18–27 mg cm−2 y−1 in the estuary, and 0.84–3.6 mg cm−2 y−1 in coastal area. Aquatic OC accumulation rates were 7.9–11.3, 0.8–1.3, and 2.6–3.1 mg cm−2 y−1, and terrestrial OC accumulation rates were 9.7–16.3, 0.02–0.14, 0.16–0.42 mg cm−2 y−1 in cores 2, 5, 6, respectively. It could be seen from the high accumulation rate of organic matter in the estuary that, when nutrients increased in the river, phytoplankton biomass and productivity would also have increased. As a result, phytoplankton sinking and organic matter sedimentation usually increased with primary productivity, resulting in the observed accumulation rate of aquatic OC in the estuary. Furthermore, terrestrial OC accumulation rates in the estuary and coastal area showed an increasing trend with the age.  相似文献   

9.
Concentrations and sinking rates of particulate biogenic silica (BSi), chlorophyll a (chl a) and phaeopigments (phae) (< 3 μm, 3–10 μm, > 10 μm and total), as well as the abundances of the major phytoplankton species, were studied during September 1991 in the Eastern Laptev Sea and the lower Lena River (Siberian Arctic). The highest chl a concentrations were found in two major “new” production regimes of the study area: (1) a deep chl a maximum (5.8 mg chl a m−3) (formed by the diatom Chaetoceros socialis) at 30 m depth on the outer shelf of the northern Laptev Sea, and (2) in the Lena River, where the phytoplankton community was dominated by fresh water diatoms (1.5 to 4.5 mg chl a m−3). Elevated chl a concentrations were also found in the river plume phytoplankton community (dominated by brackish water diatoms), NE of the Lena delta. In the Laptev Sea, the low chl a (0.1 to 3 mg chl a m−3) and high phae concentrations (0.5 to 14 mg phae m−3) indicated that the phytoplankton community (dominated by picoplanktic algae and nanoflagellates) was already senescent and affected by grazing losses. Biogenic silica values were highest in the Lena River (4 to 17 μM) as compared to the low values found in the Laptev Sea (0.3 to 4 μM). The large chl a size fraction, phae and BSi in the Lena River samples revealed the highest measured sinking rates (1.4, 2.3, and 1.5 m d−1, respectively). The formation of a strong halocline, decreasing turbulence, and possible nutrient deficiency resulted in death, disintegration and rapid sedimentation of fresh water diatoms. This was accompanied by a decrease in the BSi concentration and growth of the picoplanktic size fraction (< 3 μm) in the estuarine mixing zone (Gulf of Buorkhaya). Only a minor part of BSi was bound to intact diatom cells (< 3%) in the surface layer, most of which being apparently associated with detrital particles. In the Lena River, approximately 12% of the total silica was bound to BSi fraction, yet elsewhere in the Laptev Sea and in the estuarine mixing zone the BSi:total silica ratio was ≤ 5%. Thus, the results reflected the successional stage of a late summer phytoplankton community, characterized by dominance of small autotrophs and patchy distribution of senescent diatoms no longer able to affect the relative high levels of dissolved silica supplied by the Lena River.  相似文献   

10.
A systematic investigation of fluxes and compositions of lipids through the water column and into sediments was conducted along the U.S. JGOFS EgPac transect from l2°N to l5°S at 140°W. Fluxes of lipids out of the euphotic zone varied spatially and temporally, ranging from ≈0.20 – 0.6 mmol lipid-C m−2 day−1. Lipid fluxes were greatly attenuated with increasing water column depth, dropping to 0.002-0.06 mmol lipid-C m−2 day−1 in deep-water sediment traps. Sediment accumulation rates for lipids were ≈ 0.0002 – 0.00003 mmol lipid-C m−2 day−1. Lipids comprised ≈ 11–23% of Corg in net-plankton, 10–30% in particles exiting the euphotic zone, 2–4% particles in the deep EgPac, and 0.1-1 % in sediments. Lipids were, in general, selectively lost due to their greater reactivity relative to bulk organic matter toward biogeochemical degradation in the water column and sediment. Qualitative changes in lipid compositions through the water column and into sediments are consistent with the reactive nature of lipids. Fatty acids were the most labile compounds, with polyunsaturated fatty acids (PUFAs) being quickly lost from particles. Branchedchain C15 and C17 fatty acids increased in relative abundance as particulate matter sank and was incorporated into the sediment, indicating inputs of organic matter from bacteria. Long-chain C39 alkenones of marine origin and long-chain C20-C30 fatty acids, alcohols and hydrocarbons derived from land plants were selectively preserved in sediments. Compositional changes over time and space demonstrate the dynamic range of reactivities among individual biomarker compounds, and hence of organic matter as a whole. A thorough understanding of biogeochemical reprocessing of organic matter in the oceanic water column and sediments is, thus, essential for using the sediment record for reconstructing past oceanic environments.  相似文献   

11.
Polycyclic aromatic hydrocarbons (PAHs) were identified and measured in surface seawater and in the tissues (gills and mantle) of indigenous black mussels, Mytilus galloprovincialis, collected from three coastal sites of Saronikos Gulf (Greece), a gulf that exhibits high levels of pollution. The total PAHs measured by spectrofluorometry in the surface seawater were found in the range of 425–459 ng L−1 at the most polluted sites 1 and 2 (Elefsis Bay–Salamis Island) and in the range of 103–124 ng L−1 at site 3 (Aegina Island). PAHs' sources in seawater were identified by application of specific PAH ratios, such as phenanthrene/anthracene and fluoranthene/pyrene. Levels of PAHs in soft tissues (gills and mantle) of indigenous mussels were much higher than those reported for seawater. Total PAH concentrations in mantle tissues were in the range of 1300–1800 ng g−1 dry weight (dw) tissue at sites 1 and 2 and approximately 380 ng g−1 dw at site 3. In gill tissues total PAH concentrations were in the range of 1480–2400 ng g−1 dw at sites 1 and 2 and approximately 430 ng g−1 dw at site 3. PAHs composition was dominated by two-, three- and four-ring compounds in seawater, where 17 different PAH compounds were identified and measured in mussel tissues. Mussels can be used as sentinel organisms to monitoring PAHs' contamination, since they concentrate PAHs from the surrounding water media and therefore making the chemical analysis simpler and less prone to error than that for water. In surface seawater possible weathering and photodegradation due to hot climates contribute to reduced PAHs concentrations.  相似文献   

12.
The Laptev Sea is a high-Arctic epicontinental sea north of Siberia (Russia) that is one of the least understood regions of the world’s ocean. It is characterized by a shallow and broad shelf plateau, high influx of river water, sediments and nutrients during summer, long-lasting sea-ice cover from October to May, and the formation of a narrow flaw-lead polynya off the fast-ice edge during winter.Here, we describe results of a German–Russian research project (1993-present), presenting the distribution patterns and dynamics of its marine flora and fauna, as well as pathways and processes of coupling between sea-ice, water-column and sea-floor biota.Three ecological zones are distinguished along a combined east–west and Lena-impact gradient, differing in the composition of pelagic and benthic communities. In general, high Chl a concentrations in the sediments indicate a tight coupling between sympagic and pelagic primary production and nutrient supply to the benthos throughout the entire Laptev Sea. However, there were pronounced regional differences between the ecological zones in magnitude of primary production and trophic dynamics. Primary production during the ice-free summer was highest in the estuarine zone most strongly influenced by the Lena River (210 mg C m−2 day−1). The western and northeastern Laptev Sea yielded 55 and 95 mg C m−2 day−1, respectively. Moreover, the zones differed in the partitioning of carbon flux between zooplankton and benthic food webs. In the Lena zone zooplankton carbon demand was about 31 mg C m−2 day−1 whereas in the western zone it was 21 mg C m−2 day−1 and in the eastern zone 4 mg C m−2 day−1. Total benthic carbon demand was 32 mg C m−2 day−1 for the Lena zone, 56 mg C m−2 day−1 in the western zone and 100 mg C m−2 day−1 in the northeastern zone.A carbon budget constructed for the Laptev Sea indicates that (1) a high proportion of primary production is channelled through the benthic trophic web, bypassing the pelagic trophic web, and (2) autochthonous primary production in the northeastern and western Laptev Sea might not be sufficient to fuel both pelagic and benthic secondary production and, hence, input of allochthonous organic carbon is required to balance the overall carbon demand.  相似文献   

13.
We have investigated the chemical forms, reactivities and transformation kinetics of Fe(III) species present in coastal water with ion exchange and filtration methods. To simulate coastal water system, a mixture of ferric iron and fulvic acid was added to filtered seawater and incubated for a minute to a week. At each incubation time, the seawater sample was acidified with hydrochloric acid and then applied to anion exchange resin (AER) to separate negatively charged species (such as fulvic acid, its complexes with iron and iron oxyhydroxide coated with fulvic acid) from positively charged inorganic ferric iron (Fe(III)′). By monitoring the acid-induced Fe(III)′ over an hour, it was found that iron complexed by fulvic acid dissociated rapidly to a large extent (86–92% at pH 2), whereas amorphous ferric oxyhydroxide particles associated with fulvic acid (AFO-L) dissociated very slowly with the first-order dissociation rate constants ranging from 6.1 × 10− 5 for pH 3 to 2.7 × 10− 4 s− 1 for pH 2. Therefore, a brief acidification followed by the AER treatment (acidification/AER method) was likely to be able to determine fulvic acid complexes and thus differentiate the complexes from the AFO-L particles (the dissolution of AFO-L was insignificant during the brief acidification). The acidification/AER method coupled with a simple filtration technique suggested that the iron–fulvic acid complexes exist in both the < 0.02 μm and 0.02–0.45 μm size fractions in our coastal water system. The truly dissolved iron (< 0.02 μm) was relatively long-lived with a life-time of 14 days, probably due to the complexation by strong ligands. Such an acid-labile iron may be an important source of bioavailable iron in coastal environments, as a significant relationship between the chemical lability and bioavailability of iron has been well recognised.  相似文献   

14.
The release of ammonium from the photochemical degradation of dissolved organic matter (DOM) has been proposed by earlier studies as a potentially important remineralisation pathway for refractory organic nitrogen. In this study the photochemical production of ammonium from Baltic Sea DOM was assessed in the laboratory. Filtered samples from the Bothnian Bay, the Gulf of Finland and the Arkona Sea were exposed to UVA light at environmentally relevant levels, and the developments in ammonium concentrations, light absorption, fluorescence and molecular size distribution were followed. The exposures resulted in a decrease in DOM absorption and loss of the larger sized fraction of DOM. Analysis of the fluorescence properties of DOM using parallel factor analysis (PARAFAC) identified 6 independent components. Five components decreased in intensity as a result of the UVA exposures. One component was produced as a result of the exposures and represents labile photoproducts derived from terrestrial DOM. The characteristics of DOM in samples from the Bothnian Bay and Gulf of Finland were similar and dominated by terrestrially derived material. The DOM from the Arkona Sea was more autochthonous in character. Photoammonification differed depending on the composition of DOM. Calculated photoammonification rates in surface waters varied between 121 and 382 μmol NH4+ L− 1 d− 1. Estimated areal daily production rates ranged between 37 and 237 μmol NH4+ m− 2 d− 1, which are comparable to atmospheric deposition rates and suggest that photochemical remineralisation of organic nitrogen may be a significant source of bioavailable nitrogen to surface waters during summer months with high irradiance and low inorganic nitrogen concentrations.  相似文献   

15.
Sulfate reduction in deep coastal marine sediments   总被引：1，自引：0，他引：1  
Sulfate reduction rates in sediments of four deep stations in the Saguenay Fjord and the Laurentian Trough, Gulf of St. Lawrence, are among the lowest reported for the coastal environment. Maximum rates were 0.4–7.0 nmol cm−3 day−1. The low rates are due to relatively low sedimentation rates and continuously low temperatures. Regional differences in both integrated and maximum sulfate reduction rates in the sediment correlate with sediment trap measurements of sedimentation rate and organic carbon flux.Sulfate reduction accounts for the degradation of 5–26% of the estimated downward flux of organic matter to these sediments. Unlike the absolute rate of sulfate reduction, the relative proportion of the carbon flux that is degraded via sulfate reduction is not directly correlated with the sedimentation rate but is a function of organic matter composition, intensity of bioturbation, and the abundance of sub-oxic electron acceptors. Thus, the lowest proportion of carbon degradation via sulfate reduction occurred at a Gulf site, where a combination of low sedimentation and bioturbation rates allowed a long residence time for organic matter near the sediment surface and, in consequence, a low flux of labile carbon into the sulfate reduction zone. The highest proportion was observed at a station with a similar organic carbon flux but with higher rates of sedimentation and bioturbation. At a third site, with the highest rates of sulfate reduction as well as the highest rates of sedimentation and bioturbation, the contribution of sulfate reduction to organic matter degradation was only intermediate. This is attributable to the exhaustion of the supply of porewater sulfate. In deep coastal environments the proportion of organic matter degraded via sulfate reduction can be highly variable both spatially and temporally.  相似文献   

16.
Tangential-flow ultrafiltration was used to isolate particulate and high-molecular-weight dissolved material from seawater collected at various depths and geographic regions of the Pacific and Atlantic Oceans. Ultrafiltration proved to be a relatively fast and efficient method for the isolation of hundreds of milligrams of material. Optical and electron microscopy of the isolated materials revealed that relatively fragile materials were recovered intact. Depth-weighted results of the size distribution of organic matter in seawater indicated that ˜ 75% of marine organic carbon was low-molecular-weight (LMW) dissolved organic carbon (< 1 nm), ˜ 24% was high-molecular-weight (HMW) dissolved organic carbon (1–100 nm), and ˜ 1% was particulate organic carbon (> 100 nm). The distribution of carbon in surface water was shifted to greater relative abundances of larger size fractions, suggesting a diagenetic sequence from macromolecular material to small refractory molecules. The average C:N ratios of particulate organic matter (POM) and HMW dissolved organic matter (DOM) were 7.7 and 16.7, respectively. Differences in C:N ratios between POM and HMW DOM were large and invariant with depth and geographic region, indicating that the aggregation of HMW DOM to form POM must be of minor significance to overall carbon dynamics. The stable carbon isotope composition (δ13C) of POM averaged −22.7%. in surface water and −25.2%. in subsurface water. Several possible explanations for the observed isotopic shift with depth were explored, but we were unable to discern the cause. The δ13C of HMW DOM samples was relatively constant and averaged −21.7%., indicating a predominantly marine origin for this material. The δ15N values of POM were highly variable (5.8–15.4%.), and the availability of nitrate in surface waters appeared to be the major factor influencing δ15N values in the equatorial Pacific. In the upwelling region nitrate concentrations were relatively high and δ15N values of POM were low, whereas to the north and south of the upwelling nitrate concentrations were low and δ15N values were high. The δ15N values of HMW DOM reflected the same trends observed in the POM fraction and provided the first such evidence for biological cycling of dissolved organic nitrogen (DON). Using the observed δ15N values and an estimate of meridional advection velocity, we estimated a turnover time of 0.3 to 0.5% day−1 for HMW DON. These results suggest a major role for DON in the upper ocean nitrogen cycle.  相似文献   

17.
The fluorescence of dissolved organic matter in seawater   总被引：3，自引：0，他引：3  
A total of 28 vertical profiles of seawater fluorescence was measured in the Sargasso Sea, the Straits of Florida, the Southern California Borderlands, and the central Pacific Ocean. In all cases, surface seawater fluorescence was low as a result of photochemical bleaching which occurs on the timescale of hours. Fluorescence of deep water was 2–2.5 times higher than that of surface waters, and was constant, implying a long residence time for fluorescent organic matter, possibly of the order of thousands of years. Fluorescence correlates well with nutrients (NO3−, PO43−) in mid-depth waters (100–1000 m) in the Sargasso Sea and the central North Pacific, consistent with results in the central Pacific and the coastal seas of Japan. This suggests that regeneration or formation of fluorescent materials accompanies the oxidation and remineralization of settling organic particles.The various sources and sinks of fluorescent organic matter in the global oceans are assessed. The major sources are particles and in situ formation; rivers, rain, diffusion from sediments, and release from organisms are minor sources. The major sink is photochemical bleaching.  相似文献   

18.
Measurements of bromoform (CHBr3), diiodomethane (CH2I2), chloroiodomethane (CH2ICl) and bromoiodomethane (CH2IBr) were made in the water column (5–100 m depth) of the Southern Ocean within 0–40 km of the Antarctic sea ice during the ANTXX1/2 transect of the German R/V Polarstern, at five locations between 70–72°S and 9–11°W in the Antarctic spring/summer of 2003–2004. Some of the profiles exhibited a very pronounced layer of surface sea-ice meltwater, as evidenced by salinity minima and temperature maxima, along with surface maxima in concentrations of CHBr3, CH2I2, CH2ICl and CH2IBr. These results are consistent with in situ surface halocarbon production by ice algae liberated from the sea ice, although production within the sea ice followed by transport cannot be entirely ruled out. Additional sub-surface maxima in halocarbons occurred between 20 and 80 m. At a station further from shore and not affected by surface sea-ice meltwater, surface concentrations of CH2I2 were decreased whereas CH2ICl concentrations were increased compared to the stations influenced by meltwater, consistent with photochemical conversion of CH2I2 to CH2ICl, perhaps during upward mixing from a layer at  70 m enhanced in iodocarbons. Mean surface (5–10 m) water concentrations of halocarbons in these coastal Antarctic waters were 57 pmol l− 1 CHBr3 (range 44–78 pmol l− 1), 4.2 pmol l− 1 CH2I2 (range 1.7–8.2 pmol l− 1), 0.8 pmol l− 1 CH2IBr (range 0.2–1.4 pmol l− 1), and 0.7 pmol l− 1 CH2ICl (range 0.2–2.4 pmol l− 1). Concurrent measurements in air suggested a sea-air flux of bromoform near the Antarctic coast of between 1 and 100 (mean 32.3, median 10.4) nmol m− 2 day− 1 and saturation anomalies of 557–1082% (mean 783%, median 733%), similar in magnitude to global shelf values. In surface samples affected by meltwater, CH2I2 fluxes ranged from 0.02 to 6.1 nmol m− 2 day− 1, with mean and median values of 1.9 and 1.1 nmol m− 2 day− 1, respectively.  相似文献   

19.
In January–February 2001, we measured microbial biomass as ATP and community respiration as ETS activity of organisms < 200 μm in the aphotic zone of the Ross Sea. Microbial respiration amounted to 2.14 mmol C m− 2 day− 1 in the depth range 200–1000 m. Our daily estimates of carbon export are close to the daily percentage of net community production (NCP), removed as sinking biogenic particles from the upper 100 m in the entire Ross Sea, but lower than those of other oceanic systems. Comparing remineralization determined in this study with that obtained by sediment traps in the Ross Sea, it appeared that about 63% of organic carbon remineralized by respiration derived from POC pool. Such evidence highlighted POC source as the main organic fuel of the biological pump in the Ross Sea.  相似文献   

20.
The dynamics of dissolved inorganic carbon (DIC) and processes controlling net community production (NCP) were investigated within a mature cyclonic eddy, Cyclone Opal, which formed in the lee of the main Hawaiian Islands in the subtropical North Pacific Gyre. Within the eddy core, physical and biogeochemical properties suggested that nutrient- and DIC-rich deep waters were uplifted by 80 m relative to surrounding waters, enhancing biological production. A salt budget indicates that the eddy core was a mixture of deep water (68%) and surface water (32%). NCP was estimated from mass balances of DIC, nitrate+nitrite, total organic carbon, and dissolved organic nitrogen, making rational inferences about the unobserved initial conditions at the time of eddy formation. Results consistently suggest that NCP in the center of the eddy was substantially enhanced relative to the surrounding waters, ranging from 14.1±10.6 (0–110 m: within the euphotic zone) to 14.2±9.2 (0–50 m: within the mixed layer) to 18.5±10.7 (0–75 m: within the deep chlorophyll-maximum layer) mmol C m−2 d−1 depending on the depth of integration. NCP in the ambient waters outside the eddy averaged about 2.37±4.24 mmol C m−2 d−1 in the mixed layer (0–95 m). Most of the enhanced NCP inside the eddy appears to have accumulated as dissolved organic carbon (DOC) rather than exported as particulate organic carbon (POC) to the mesopelagic. Our results also suggest that the upper euphotic zone (0–75 m) above the deep chlorophyll maximum is characterized by positive NCP, while NCP in the lower layer (>75 m) is close to zero or negative.  相似文献   

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