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1.
In addition to previously analyzed sediments of Cenomanian to Santonian age in the Tarfaya Sondage No. 2 well, this study presents the results of a stratigraphically younger interval of Santonian to Early Campanian age in the adjacent well Tarfaya Sondage No. 1. This interval is part of the oceanic anoxic event 3 (OAE3), which occurred mainly in the Atlantic realm. Due to known high quality source rocks related to OAEs (i.e. Cenomanian–Turonian), the investigated sample section was tested for the quality, quantity and kind of organic matter (OM), describing also the depositional environment. The study was carried out by means of (i) elemental analysis (Corg, CaCO3, TS), (ii) Rock–Eval pyrolysis, (iii) vitrinite reflectance measurements, (iv) gas chromatography-flame ionization detection (GC-FID) and (v) GC-mass spectrometry (GC–MS). Total content of organic carbon (Corg), values for the hydrogen index (HI) (mainly in the range 500–700 mg/g Corg) and S2 values (10–40 mg/g rock), support the assumption of a high petroleum generation potential in these Upper Cretaceous sediments. TS/Corg ratios as well as pristane/phytane ratios indicate variable oxygen contents during sediment deposition, representing a typical depositional setting for the Late Cretaceous and are in good agreement with previously analyzed data in the Tarfaya Basin. Phyto- and zoo-plankton were identified as marine sourced. All of the investigated Early Campanian and Santonian samples are immature with some tendencies to early maturation. These results are based on vitrinite reflectance (0.3–0.4% VRr), Tmax values (409–425 °C), production indices (PI; S1/(S1 + S2)< 0.1) and n-alkane ratios (i.e. carbon preference index). As the deposition of these sediments is time related to OAE3, the depositional environment was characterized by oxygen-deficiency or even anoxic bottom water conditions. This situation was favored during the Cretaceous greenhouse climate by limited oxygen solubility in the then warmer ocean water. Furthermore, local factors related to nutrient supply and primary bioproductivity led to the exceptionally thick, Upper Cretaceous organic matter-rich sedimentary sequence of the Tarfaya Basin.  相似文献   

2.
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   

3.
Sediments were sampled and oxygen profiles of the water column were determined in the Indian Ocean off west and south Indonesia in order to obtain information on the production, transformation, and accumulation of organic matter (OM). The stable carbon isotope composition (δ13Corg) in combination with C/N ratios depicts the almost exclusively marine origin of sedimentary organic matter in the entire study area. Maximum concentrations of organic carbon (Corg) and nitrogen (N) of 3.0% and 0.31%, respectively, were observed in the northern Mentawai Basin and in the Savu and Lombok basins. Minimum δ15N values of 3.7‰ were measured in the northern Mentawai Basin, whereas they varied around 5.4‰ at stations outside this region. Minimum bottom water oxygen concentrations of 1.1 mL L?1, corresponding to an oxygen saturation of 16.1%, indicate reduced ventilation of bottom water in the northern Mentawai Basin. This low bottom water oxygen reduces organic matter decomposition, which is demonstrated by the almost unaltered isotopic composition of nitrogen during early diagenesis. Maximum Corg accumulation rates (CARs) were measured in the Lombok (10.4 g C m?2 yr?1) and northern Mentawai basins (5.2 g C m?2 yr?1). Upwelling-induced high productivity is responsible for the high CAR off East Java, Lombok, and Savu Basins, while a better OM preservation caused by reduced ventilation contributes to the high CAR observed in the northern Mentawai Basin. The interplay between primary production, remineralisation, and organic carbon burial determines the regional heterogeneity. CAR in the Indian Ocean upwelling region off Indonesia is lower than in the Peru and Chile upwellings, but in the same order of magnitude as in the Arabian Sea, the Benguela, and Gulf of California upwellings, and corresponds to 0.1–7.1% of the global ocean carbon burial. This demonstrates the relevance of the Indian Ocean margin off Indonesia for the global OM burial.  相似文献   

4.
We study fish scales as a proxy of fish abundance and preservation biases together with phosphorus from fish remains (Pfish) in a sediment core retrieved off Callao, Peru (12°1′S, 77°42′W; water depth=179 m; core length=52 cm). We interpret our results as a function of changing redox conditions based on ratios of redox-sensitive trace elements (Cu/Al, Mo/Al, Ni/Al, Zn/Al, V/Al), terrigenous indicators (Fe in clays, Ti, Al), and biogenic proxies (CaCO3, biogenic opal, total nitrogen, organic carbon, barite Ba). The core covers roughly 700 years of deposition, based on 210Pb activities extrapolated downcore and 14C dating at selected intervals. Our fish-scale record is dominated by anchovy (Engraulis ringens) scales followed by hake (Merluccius gayii) scales.The core presented an abrupt lithological change at 17 cm (corresponding to the early 19th century). Above that depth, it was laminated and was more organic-rich (10–15% organic carbon) than below, where the core was partly laminated and less organic-rich (<10%). The lithological shift coincides with abrupt changes in dry bulk density and in the contents of terrigenous and redox-sensitive trace elements, biogenic proxies, and fish scales. The remarkable increase in redox-sensitive trace elements in the upper 17 cm of the core suggests more reducing conditions when compared with deeper and older horizons, and is interpreted as an intensification of the oxygen minimum zone off Peru beginning in the early 19th century. Higher fish-scale contents and higher Pfish/Ptotal ratios were also observed within the upper 17 cm of the core. The behavior of biogenic proxies and redox-sensitive trace elements was similar; more reduced conditions corresponded to higher contents of CaCO3, Corg, total nitrogen and fish scales, suggesting that these proxies might convey an important preservation signal.  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.
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   

7.
《Marine Chemistry》2007,103(1-2):30-45
The chemistry of dissolved Fe(III) was studied in the Scheldt estuary (The Netherlands). Two discrete size fractions of the dissolved bulk (< 0.2 μm and < 1 kDa) were considered at three salinities (S = 26, 10 and 0.3).Within the upper estuary, where fresh river water meets seawater, the dissolved Fe concentration decreases steeply with increasing salinity, for the fraction < 0.2 μm from 536 nM at S = 0.3 to 104 nM at S = 10 and for the fraction < 1 kDa from 102 nM to 36 nM Fe. Further downstream, in the middle and lower estuary, this decrease in the Fe concentration continues, but is far less pronounced. For all samples, the traditionally recognised dissolved strong organic Fe-binding ligand concentrations are lower than the dissolved Fe concentrations.Characteristics of dissolved Fe-binding ligands were determined by observing kinetic interactions with adsorptive cathodic stripping voltammetry. From these kinetic experiments we concluded that apart from the well-known strong Fe-binding organic ligands (L, logK′ = 19–22) also weak Fe-binding ligands (P) existed with an α value (binding potential = K′ · [P]) varying between 1011.1 and 1011.9. The presence of this relatively weak ligand explained the high concentrations of labile Fe present in both size fractions in the estuary. This weak ligand can retard or prevent a direct precipitation after an extra input of Fe.The dissociation rate constants of the weak ligand varied between 0.5 × 10− 4 and 4.3 × 10− 4 s− 1. The rate constants of the strong organic ligand varied between kd = 1.5 × 10− 3–17 × 10− 2 s− 1 and kf = 2.2 × 108–2.7 × 109 M− 1 s− 1. The dissociation rate constant of freshly amorphous Fe-hydroxide was found to be between 4.3 × 10− 4 and 3.7 × 10− 3 s− 1, more labile or equal to the values found by Rose and Waite [Rose, A.L., Waite, T.D., 2003a. Kinetics of hydrolysis and precipitation of ferric iron in seawater. Environ. Sci. Technol., 37, 3897–3903.] for freshly precipitated Fe in seawater.Kinetic rate constants of Fe with the ligand TAC (2-(2-Thiazolylazo)-p-cresol) were also determined. The formation rate constant of Fe(TAC)2 varied between 0.1 × 108 and 3.6 × 108 M− 1 s− 1, the dissociation rate constant between 0.2 × 10− 5 and 17 × 10− 5 s− 1 for both S = 26 and S = 10. The conditional stability constant of Fe(TAC)2 (βFe(TAC)2′) varied between 22 and 23.4 for S = 10 and S = 26 more or less equal to that known from the literature (logβFe(TAC)2′ = 22.4; [Croot, P.L., Johansson, M., 2000. Determination of iron speciation by cathodic stripping voltammetry in seawater using the competing ligand 2-(2-Thiazolylazo)-p-cresol (TAC). Electroanalysis, 12, 565–576.]). However, at S = 0.3 the logβFe(TAC)2′ was 25.3, three orders of magnitude higher. Apparently the application of TAC to samples of low salinity can only be done when the correct βFe(TAC)2′ is known.  相似文献   

8.
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   

9.
Determinations of the activity of the respiratory electron transport system (ETS), during the FRAM III expedition permit us to estimate oxygen utilization rates (RO2) from the surface to 2000 m under the polar pack ice in the Nansen Basin just north of Svalbard (83°N, 7°E) during April 1981. We found RO2 at in situ temperatures ranging from 20 pM O2 min−1 just below the ice to 0.2 pM O2 min−1 at 2000 m. These rates are low compared to most other ocean regions, but they could decrease particulate organic carbon and nitrogen by 76% and 74%, respectively, over a period of ∼6 months. The RO2 calculations based on measurements made at 0 °C yielded a power function of RO2 vs. depth (Z) of RO2=67Z−0.5534. When this RO2 profile was superimposed on a more recent oxygen utilization rate profile made using the 3He–3H–AOU method (OUR), in the same vicinity of the Nansen Basin during 1987 (OUR=52Z–0.4058, [Zheng, Y., Schlosser, P., Swift, J.W., Jones, E.P., 1997. Oxygen utilization rates in the Nansen Basin, Arctic Ocean: implications for new production. Deep Sea Research I 44, 1923–1943]), the agreement of the two profiles was close. On one hand, this was to be expected because RO2 is the biological basis of OUR, on the other hand, it was a surprise because the methodologies are so different. Nitrate mineralization obtained from ETS activities also compared favorably with calculations based on the data of Zheng et al. [1997. Oxygen utilization rates in the Nansen Basin, Arctic Ocean: implications for new production. Deep Sea Research I 44, 1923–1943]. Chlorophyll ranged from 6 ng L−1 at 5 m to 0.06 ng L−1 at 2000 m. Particulate organic carbon (POC) decreased from 0.93 μM C just below the ice to less than 0.4 μM C at 500 m. Particulate organic nitrogen (PON) was not detectable below 70 m, however in the upper 70 m it ranged from 0.16 to 0.04 μM N. The C/N mass ratio over these depths ranged from 5.8 to 11.3. Annual carbon productivity as calculated to balance the total water column respiration was 27 g C m−2 y−1. The integrated respiration rate between 50 and 4000 m suggests that exported production and carbon flux from the 50 m level was 24 g C m−2 y−1. These are minimal estimates for the southern Nansen Basin because they are based on measurements made at the end of the Arctic winter.  相似文献   

10.
Mass fluxes of diatom opal, planktonic foraminifera carbonate and coccolithophorid carbonate were measured with time-series sediment traps at six sites in the Arabian Sea, Bay of Bengal and Equatorial Indian Ocean (EIOT). The above fluxes were related to regional variations in salinity, temperature and nutrient distribution. Annual fluxes of diatom opal range between 3 and 28 g m−2 yr−1, while planktonic foraminifera carbonate fluxes range between 6 and 23 g m−2 yr−1 and coccolithophorid carbonate fluxes range between 4 and 24 g m−2 yr−1. Annual planktonic foraminifera carbonate to coccolithophorid carbonate ratios range between 0.8 and 2.2 and coccolithophorid carbonate to diatom opal ratios range between 0.5 and 3.3.In the western Arabian Sea, coccolithophorids are the major contributors to biogenic flux during periods of low nutrient concentrations. Coccolithophorid carbonate fluxes decrease and planktonic foraminiferal carbonate and diatom opal fluxes increase when nutrient-rich upwelled waters are advected over the trap site. In the oligotropic eastern Arabian Sea, coccolithophorid carbonate fluxes are high throughout the year. Planktonic foraminiferal carbonate fluxes are the major contributors to biogenic flux in the EIOT. In the northern and central Bay of Bengal, when surface salinity values drop sharply during the SW monsoon, there is a drastic reduction in planktonic foraminiferal carbonate fluxes, but coccolithophorid carbonate and diatom opal fluxes remain steady or continue to increase. Distinctly higher annual molar Sibio/Cinorg (>1) and Corg/Cinorg (>1.5) ratios are observed in the northern and central Bay of Bengal mainly due to lower foraminiferal carbonate production as a result of sharp salinity variations. We can thus infer that the enhanced freshwater supply from rivers should increase oceanic CO2 uptake. Its silicate supply favours the production of diatoms while the salinity drop produces conditions unfavourable for most planktonic foraminifera species.  相似文献   

11.
Temporal and spatial variations in the composition of particulate organic matter (POM) from Florida Bay, USA were examined. The predominance of short-chain homologues for n-alkanes, n-alcohols and n-fatty acids as well as relatively high abundance of C27 and C28 sterols suggested that an autochthonous/marine source of OM was dominant bay-wide. Several biomarker proxies such as Paq [(C23 + C25)/(C23 + C25 + C29 + C31) n-alkanes], short/long chain n-alkanes, (C29 + C31) n-alkanes and taraxerol indicated a spatial shift in OM sources, where terrestrial OM rapidly decreased while seagrass and microbial OM markedly increased along a northeastern to southwestern transect. Regarding seasonal variations, POM collected during the dry season was enriched in terrestrial constituents relative to the wet season, likely as a result of reduced primary productivity of planktonic species and seagrasses during the dry season. Principal component analysis (PCA) classified the sample set into sub-groups based on PC1 which seemed to be spatially controlled by OM origin (terrestrial-mangrove vs. marine-planktonic/seagrass). The PC2 seemed to be more seasonally controlled suggesting that hydrological fluctuations and seasonal primary productivity are the drivers controlling the POM composition in Florida Bay.  相似文献   

12.
The distribution of transparent exopolymer particles (TEP) was investigated during a coccolithophorid bloom in the northern Bay of Biscay (North Atlantic Ocean) in early June 2006. MODIS chlorophyll-a (Chl-a) and reflectance images before and during the cruise were used to localize areas of important biological activity and high reflectance (HR). TEP profiles along the continental margin, determined using microscopic (TEPmicro) and colorimetric (TEPcolor) methods, showed abundant (6.1×106–4.4×107 L?1) and relatively small (0.5–20 μm) particles, leading to a low total volume fraction (0.05–2.2 ppm) of TEPmicro and similar vertical profiles of TEPcolor. Estimates of carbon content in TEP (TEP-C) derived from the microscopic approach yielded surface concentration of 1.50 μmol C L?1. The contribution of TEP-C to particulate organic carbon (POC) was estimated to be 12% (molar C ratio) during this survey. Our results suggest that TEP formation is a probable first step to rapid and efficient export of C during declining coccolithophorid blooms.  相似文献   

13.
Pinna nobilis is the largest endemic bivalve of the Mediterranean Sea, declared protected since 1992. Although hydrodynamic stress induced by waves is known to influence density, size and orientation of P. nobilis, the effect of other hydrological features is unknown. This paper considers a P. nobilis population living within a Posidonia oceanica meadow in the Gulf of Oristano (Sardinia, Italy). We hypothesize that spatial differences in density and orientation of P. nobilis may be related to significant wave height (HS), wave direction (DW), bottom current direction (DBC) and bottom current speed (SBC). A population of P. nobilis was investigated at different sites and its distribution was correlated to hydrodynamics by means of a numerical modeling approach. The spatial distribution was patchy, with a density of 0.06–6.7 ind. 100 m− 2. A non-uniform distribution of shell orientations (OS) was demonstrated in 4 sites out of 6. DBC and SBC were the main factors affecting OS, while waves had little influence. A SBC of 0.07 m s− 1 appears to be the threshold for inducing specimen directionality with shells aligned to the current and the ventral side exposed to the flow. This suggests that feeding strategy is a key factor in determining OS, in addition to drag minimization. We also highlighted the role of adjacent lagoons in supporting high densities as a result of high food availability. These findings demonstrate the usefulness of modeling techniques in explaining the spatial distribution pattern of P. nobilis and in contributing to our knowledge of its ecological traits.  相似文献   

14.
Remineralization ratios (–O2:P, Corg.:P, N:P) in the ocean are estimated from ocean tracer data using a new approach, which takes into account the effects of local exchange across neutral surfaces. This approach is applied to temperature, salinity, phosphate, nitrate, dissolved oxygen, alkalinity, and dissolved inorganic carbon data from the low- and mid-latitude Pacific, Indian, and South Atlantic Oceans. The consideration of local exchange effects tends to reduce the –O2:P and Corg.:P remineralization estimates above 1500 m compared to earlier estimates. Below 1500 m, exchange effects can be neglected (except in the South Atlantic) and earlier estimates appear robust. In the deep South Atlantic, the consideration of these effects leads to increased –O2:P and Corg.:P remineralization ratio estimates, bringing them more in line with the robust deep ocean estimates. For reasonable, open ocean mixing coefficient values and several choices for phosphate remineralization rate profiles, –O2:P (Corg.:P) remineralization ratios in the ocean increase from about 140 (100) at 750 m depth to about 170 (130) at 1500 m and remain so deeper down. Such an increase down through the upper ocean thermocline implies significant fractionation during remineralization of organic matter—nutrients are released higher in the water column than inorganic carbon. These results also argue for a –O2:P (Corg.:P) uptake ratio in new production of about 140–150 (100–110). N:P remineralization ratios decrease from about 15 at 750 m to about 12 at 1500–2000 m. This may reflect a “true” N:P remineralization (and uptake) ratio of about 16, modified by denitrification.These results imply that applications of derived, quasi-conservative tracers, based on the assumption of constant remineralization ratios, may be subject to significant error for depths less than 1500 m. In addition, present Ocean General Circulation Models of the natural carbon cycle in the ocean–atmosphere system assume remineralization to occur without fractionation but have problems simulating observed, pre-industrial levels of atmospheric pCO2, given observed ocean inventories of alkalinity and dissolved inorganic carbon. Implementation of uptake and (depth-dependent) remineralization ratios estimated here would likely reduce this problem considerably. Furthermore, calculations with a simple global carbon cycle model show that fractionation in the modern ocean, as estimated in the present work, has reduced atmospheric pCO2 by more than 20 ppm below the level it would have had without fractionation.  相似文献   

15.
Benthic fluxes of dissolved inorganic carbon, total alkalinity, oxygen, nutrients, nitrous oxide and methane were measured in situ at three sites of Río San Pedro salt marsh tidal creek (Bay of Cádiz, SW Spain) during three seasons. This system is affected by the discharges of organic carbon and nutrients from the surrounding aquaculture installations. Sediment oxygen uptake rates and inorganic carbon fluxes ranged respectively from 16 to 79 mmol O2 m? 2 d? 1 and from 48 to 146 mmol C m? 2 d? 1. Benthic alkalinity fluxes were corrected for the influence of NH4+ and NO3? + NO2? fluxes, and the upper and lower limits for carbon oxidation rates were inferred by considering two possible scenarios: maximum and minimum contribution of CaCO3 dissolution to corrected alkalinity fluxes. Average Cox rates were in all cases within ± 25% of the upper and lower limits and ranged from 40 to 122 mmol C m? 2 d? 1. Whereas carbon mineralization did not show significant differences among the sites, Cox rates varied seasonally and were correlated with temperature (r2 = 0.72). During winter and spring denitrification was estimated to account for an average loss of 46% and 75%, respectively, of the potentially recyclable N, whereas during the summer no net removal was observed. A possible shift from denitrification to dissimilatory nitrate reduction to ammonium (DNRA) during this period is argued. Dissolved CH4 and N2O fluxes ranged from 5.7 to 47 μmol CH4 m? 2 d? 1 and 4.3 to 49 μmol N–N2O m? 2 d? 1, respectively, and represented in all cases a small fraction of total inorganic C and N flux. Overall, about 60% of the total particulate organic matter that is discharged into the creek by the main fish farm facility is estimated to degrade in the sediments, resulting in a significant input of nutrients to the system.  相似文献   

16.
Seawater samples were collected for microbial analyses between 55 and 235 m depth across the Arctic Ocean during the SCICEX 97 expedition (03 September–02 October 1997) using a nuclear submarine as a research platform. Abundances of prokaryotes (range 0.043–0.47×109 dm−3) and viruses (range 0.68–11×109 dm−3) were correlated (r=0.66, n=150) with an average virus:prokaryote ratio of 26 (range 5–70). Biomass of prokaryotes integrated from 55 to 235 m ranged from 0.27 to 0.85 g C m−2 exceeding that of phytoplankton (0.005–0.2 g C m−2) or viruses (0.02–0.05 g C m−2) over the same depth range by an order of magnitude on average. Using transmission electron microscopy (TEM), we estimated that 0.5% of the prokaryote community on average (range 0–1.4%) was visibly infected with viruses, which suggests that very little of prokaryotic secondary production was lost due to viral lysis. Intracellular viruses ranged from 5 to >200/cell, with an average apparent burst size of 45±38 (mean±s.d.; n=45). TEM also revealed the presence of putative metal-precipitating bacteria in 8 of 13 samples, which averaged 0.3% of the total prokaryote community (range 0–1%). If these prokaryotes are accessible to protistan grazers, the Fe and Mn associated with their capsules might be an important source of trace metals to the planktonic food web. After combining our abundance and mortality data with data from the literature, we conclude that the biomass of prokaryoplankton exceeds that of phytoplankton when averaged over the upper 250 m of the central Arctic Ocean and that the fate of this biomass is poorly understood.  相似文献   

17.
The macrotidal bay of Marennes-Oléron is the most important French site for shellfish production (oysters and mussels); yet the primary productivity of the phytoplankton compartment in this system is not well known. In this study, photosynthetic parameters were determined using 14C incubations of bottom and surface water samples, during fall, winter and summer (2001–2002), along a north–south transect in the bay. Estimates of primary productivity showed that water column primary production is light-limited in the bay and that a BZpI0 type model can be applied. Spatial differences existed in the bay, with a more productive northern zone and less productive river area. With a water column primary production of 185 g C m−2 yr−1, Marennes-Oléron Bay lies in the mean range for phytoplankton primary production capacity among European and North American estuaries.  相似文献   

18.
Distribution coefficients, iKFe, were measured for sorption of yttrium and the rare earth elements (YREEs) on hydrous ferric oxide (HFO) in 0.5 M NaCl solutions over the pH range 3.9–8.4 (T = 25 °C). An existing, non-electrostatic model [Quinn, K.A., Byrne, R.H., Schijf, J., 2006. Sorption of yttrium and rare earth elements by amorphous ferric hydroxide: influence of pH and ionic strength. Mar. Chem. 99, 128–150] was modified to account for sorption of YREE–chloride complexes, as well as YREE–hydroxide complexes at elevated pH. The extended model, which allows calculation of iKFe as a function of [H+], contains two parameters, SK1 and SK2, to describe the equilibrium between positive, neutral, and negative forms of the hydroxyl functional groups on the HFO surface. In addition, it contains several composite, conditional stability constants, An, that represent YREE bonding to the neutral groups with release of n protons and/or to the negatively charged groups with release of n ? 1 protons.In 0.5 M NaCl solutions, YREE sorption on HFO is weaker and less pH dependent, yielding only 0.7–0.9 protons per YREE cation on average, vs. about 1.5 at low ionic strength. This is due to enhanced deprotonation of the HFO surface (SK1 ~ 0, pSK2 = 6.16), leading to an increase in the proportion of negatively charged groups, which release fewer protons per YREE cation sorbed. On a logarithmic scale, iKFe is a nearly linear function of pH, except at pH > 8 where cumulative sorption of YREE–hydroxide complexes causes it to rise more rapidly, especially for the heavy REEs. Both our own data and prior results from the literature are well described by the extended model, using only three adjustable parameters, A1–A3. The constant A3, representing YREE bonding to the negatively charged groups with release of two protons, shows an excellent linear free-energy relation when plotted against the first YREE hydrolysis constant, β1*. There is no evidence for YREE bonding to the positively charged groups (i.e., A0 = 0).  相似文献   

19.
The giant diatom Ethmodiscus was examined along an east–west transect at 28–30°N during 2002 and 2003 to determine if abundance, chemical composition or physiological status of this largest of diatoms varied on the scale of 100's–1000's of km in North Pacific gyre. Abundance ranged from <0.1–>2.0 cells m−3 and supported the notion of an abundance mosaic reported previously. However, there was only minimal support for the relationship between abundance and nutrient concentration at 125 m reported previously. Cellular chlorophyll varied little along the transect (7.3–10.9 ng chl cell−1) except at the westernmost station. Cellular N and P quotas co-varied 3–4.5 fold (mean=50.8±3.7 and 3.7±0.8 nmol N and P cell−1) and yielded N:P ratios that closely clustered around the Redfield ratio (average=14.6±1.1). Only low levels of chlorophyll-normalized alkaline phosphatase (APase) activity were observed (0.4–2.5 nmol P μg chl−1 h−1) with APase activity lower than that in either the bulk water, or co-occurring Trichodesmium spp. and Pyrocystis noctiluca. The active fluorescence parameter Fv:Fm, a property sensitive to Fe stress, was uniformly high at all stations (average=0.73±0.04 for 2003, and 0.69±0.05 for 2002), indicating sufficient Fe for optimum photosynthetic competence. These results contrasted sharply with results from Rhizosolenia mats reported along the same transect where there was a significant decline westward in Fv:Fm. Both ferredoxin (Fd) and flavodoxin accumulated in cells of Ethmodiscus, resulting in Fd Index values of<0.6. Iron cell quotas ranged from 0.7–5.1 pmol Fe cell−1. When normalized to cytoplasmic volume, the Fe μm−3 was comparable to that of Escherichia coli. We note that the disproportionate contribution of the vacuole (with its high organic content) to total volume typical of large diatoms is a potentially significant source of error in Fe:C ratios and suggest that Fe should be normalized to cytoplasmic volume whenever possible to permit valid intercomparisons between studies. The composition, Fv:Fm data and Fe:C ratio suggest a relatively uniform population experiencing little N, P or Fe stress. The uncoupling of the Fd Index from these measures is consistent with previous findings showing that the expression of flavodoxin can be characterized as an early stress response and that its accumulation is not necessarily correlated with physiological deficit. Ethmodiscus appears to be well adapted to some of the most oligotrophic waters in the ocean. Because it is an important sedimentary marker, the biology of living Ethmodiscus provides insights into the source of extensive Ethmodiscus oozes. Mass sedimentation after frontal accumulation has been suggested as a source for these oozes. Our data contain no evidence that the flux is linked directly to Fe, N or P stress.  相似文献   

20.
This one-year survey conducted in the macrotidal estuary of Penzé (Brittany, Western part of the Channel, France) was aimed at examining the variations of the various dissolved and particulate copper species. Ten field stations along the whole freshwater–seawater mixing zone were sampled each month. Different biogeochemical parameters (SPM, chl-a, pH and DOC) were also measured. The levels in total dissolved and total particulate copper ranged from 1.8 to 9.5 nM and from 5 to 98 μg g−1, respectively; such amounts are indicative of a pollution-free system. Extractable C18 copper (non-polar hydrophobic organic copper species), in winter and spring, accounted for 30–40% of the total dissolved copper. In summer, this contribution rapidly rose to 60% in the salinity range 20–30; over the same period of time, total particulate copper decreased. The change in dissolved copper speciation and the lowering of particulate copper concentrations were attributed to the release of strong organic ligands by phytoplankton. Our field data evidenced a highly variable behaviour for the various copper species over the seasonal cycle, and then led us to identify the following mechanisms: (i) metal desorption from organic river-flown particles (winter and spring), (ii) metal desorption from resuspended sediment in the upstream section (summer), (iii) competition between particles, non-extractable C18 organic ligands and phytoplankton-released extractable C18 organic ligands to complex copper in the downstream section (summer), and (iv) removal of non-extractable C18 organic copper by adsorption (autumn). Dissolved copper species fluxes were assessed: most of metal inputs to the estuary (60–74%) corresponded to non-extractable C18 organic copper. Winter and spring metal output fluxes were mainly constituted of non-extractable C18 organic complexes; on the other hand, extractable C18 organic complexes were predominant in summer and autumn output fluxes.  相似文献   

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