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1.
The distribution of species is shifting in response to recent climate change. Changes in the abundance and distributions of habitat‐forming species can have knock‐on effects on community structure, biodiversity patterns and ecological processes. We empirically examined temporal changes in the abundance of the warm‐water kelp Laminaria ochroleuca at its poleward range edge in the Western English Channel. Resurveys of historical sites indicated that the abundance of L. ochroleuca has increased significantly in recent decades. Moreover, examination of historical records suggested that L. ochroleuca has extended its distribution from sheltered coasts on to moderately wave‐exposed open coasts, where it now co‐exists and competes with the assemblage dominant Laminaria hyperborea. Proliferation of L. ochroleuca at its poleward range edge corresponds with a period of rapid warming in the Western English Channel. Preliminary comparisons between L. ochroleuca and L. hyperborea highlighted some subtle but ecologically significant differences in structure and function. In summer, the average biomass of epiphytic stipe assemblages on L. hyperborea was 86 times greater than on L. ochroleuca whereas, on average, L. ochroleuca had a greater stipe length and its blade supported 18 times as many gastropod grazers (Gibbula cineraria). Differences in summer growth rates were also recorded, with L. ochroleuca being more productive than L. hyperborea throughout July. Comprehensive seasonally replicated comparisons are needed to examine the wider implications of proliferation of L. ochroleuca at its poleward range edge, but our study suggests that local biodiversity patterns and ecological processes (e.g. timing of productivity and trophic pathways) on shallow subtidal reefs may be altered by shifts in the relative abundances of habitat‐forming kelp species.  相似文献   

2.
Toward assessing the biogeochemical significance of seaweeds in relation to dissolved iodine in seawater, the effect of whole seaweeds (Laminaria digitata and Fucus serratus) upon iodide and iodate, at essentially natural concentrations, has been studied. The weeds were carefully removed from the sub-littoral zone of the Menai Straits and exposed to iodide and iodate at their natural temperature (6 °C), but under continuous illumination. Laminaria digitata was found to decrease the concentration of iodate with an exponential rate constant of 0.008–0.24 h−1. This is a newly discovered process which, if substantiated, will require an entirely new mechanism. Generally, apparent iodide concentration increased except in a run with seawater augmented with iodide, where it first decreased. The rate constant for loss of iodide was 0.014–0.16 h−1. Meanwhile, F. serratus was found not to decrease iodate concentrations, as did L. digitata. Indeed, after ∼30 h iodate concentrations increased, suggesting that the weed may take in iodide before oxidising and releasing it. If substantiated, this finding may offer a way into one of the most elusive of processes within the iodine cycle – iodide oxidation. With both seaweeds sustained long-term increases of apparent iodide concentration are most easily explained as a secretion by the weeds of organic matter which is capable of reducing the Ce(IV) reagent used in determination of total iodine. Modelling of the catalytic method used is provided to support this contention. The possibility of developing this to measure the strain that seaweeds endure in this kind of biogeochemical flux experiment is discussed. A Chemical Oxygen Demand type of approach is applied using Ce(IV) as oxidant. The results of the iodine experiments are contrasted with the several investigations of 131I interaction with seaweeds, which have routinely used discs of weed cut from the frond. It is argued that experiments conducted with stable iodine may measure a different variable to that measured in radio-iodine experiments.  相似文献   

3.
A number of field and laboratory studies on the impact of marine macroalgae on dissolved inorganic iodine speciation are presented. Within tidally isolated rock pools, the brown macroalga Fucus serratus was found to both release stored iodide and to facilitate the reduction of iodate to iodide. In contrast, no discernible changes in iodine speciation were observed in rock pools containing green macroalgae of the genus Ulva. Incubation experiments confirmed that the macroalgae Laminaria digitata, F. serratus and Kallymenia antarctica release iodide, though the rate of release varied between species and between specimens of the same species. Application of oxidative stress by treatment with cell wall derived oligoguluronate elicitors increased the efflux of iodide by L. digitata approximately 20-fold. The release of iodide by macroalgae may impact upon the formation of volatile iodine species (molecular iodine and iodocarbons) that are of importance in the coastal atmosphere.  相似文献   

4.
Physiology of Laminaria   总被引：1，自引：0，他引：1  
Abstract. Sporophytes of Laminaria digitata and L. saccharina were collected from the shore at different times of year. Intact sporophytes of both species, and discs cut from L. digitata lamina tissue were maintained for several weeks in laboratory cultures under various nitrate, phosphate, temperature and daylength regimes. Substrate-saturated uptake rates of approximately 24 μgN g dry weight-1 h-1 from 20 μM nitrate and 8 μgP g dry weight-1 h-1 from 10 μM phosphate were more than sufficient to account for internal nitrogen and phosphorus accumulation. Other nitrogen sources - nitrite, ammonium and urea - were also taken up, independently of each other, and supported growth. During the late spring decline of ambient nutrient levels, when growth rates on the shore also decline markedly, enrichment with nitrate (15 μM) and phosphate (3μ) together prevented this decline and also maintained peak photosynthetic rates (net photosynthesis = 10.4 μlO2 cm-2 h-1) which otherwise dropped to 4.5 μO2 cm-2 h-1 over 47 days at ambient nutrient levels (0.5 μM nitrate and phosphate). Slow summer growth rates in June/July were enhanced to greater than spring peak values by combined nitrate (7.5 μM) and phosphate (1.8 μM) enrichment; neither was sufficient alone, although the individual nutrients were accumulated internally. A lesser, but significant enhancement was also achieved in September. In midwinter, nutrient enhancement itself (10.5 μM nitrate and 3.0 μM phosphate) had a small effect on growth rates only if summer water temperature (15°C) was used, but the dramatic effect of an increased photoperiod (7.5 to 17.5 h) was in excess of that expected for the increased radiant energy available. This was found to be due, at least in L. digitaia discs, to the re-establishment of a surface meristoderm in the dormant winter tissue; this was particularly active with high phosphate supply. Growth of the new lamina in January on the shore was much reduced if the old lamina was removed, although the time of initiation of new growth remained unchanged. In the laboratory, the old lamina was found to be a source of nitrogen for new lamina but not of fixed carbon or phosphorus. New lamina photosynthesis, manifest as mannitol accumulation, was directly proportional to phosphate supply up to at least 7.5 μM phosphate. Mannitol accumulation was then suppressed by a nitrate supply above 12 um, presumably by diversion of fixed carbon to other biosynthetic pathways.  相似文献   

5.
Iodide oxidation to iodate in near-surface waters of the open oceans is an elusive process, and an unequivocal demonstration of it would simplify modelling of the marine iodine system. In the open ocean, the upward advection of iodate complicates any mathematical treatment of the problem. In this context, the high concentration (0.1 μM) of iodate in the Black Sea surface waters suggested that this Sea might be a place where oxidation might be demonstrated. Hydrologically, the surface waters of the Black Sea appear to be downstream of the deeper waters and, given the latter's anoxicity, the surface waters seemed likely to gain most of their iodine as iodide by upward advection. To test this further, prior to experimentation, an iodine budget for the near-surface waters, based upon the latest hydrological model of the Sea was prepared; this predicts a minimum oxidation flux of 3.89×10−4 mol I m−2 a−1. The chemistry of this oxidation is discussed in the light of existing knowledge of the sulfide system. It is argued that as the redox potential of the IO3−/I− and I2/I− couples at pHs typical of the Black Sea (7.75) are much higher than that of the sulfate–sulfide couple, iodide is probably oxidized in the near-surface domain. This contrasts with sulfide oxidation in the suboxic zone. The possible role of nitrifying bacteria in the oxidation is discussed.  相似文献   

6.
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7.
Photochemical production rates of hydrogen peroxide (H2O2) were determined in Antarctic waters during two research cruises. The first cruise was from mid-October to mid-November, 1993, in the confluence of the Weddell and Scotia Seas, and the second cruise was in December, 1994, along the coast of the Antarctic Peninsula. During these cruises, midday sea-surface production rates ranged from 2.1 to 9.6 nM h−1, with an average rate of 4.5 nM h−1. Production rates were consistently smaller than rates determined at lower latitudes (>9 nM h−1), primarily due to the colder temperatures and lower ultraviolet irradiances in polar waters. In situ production rates were determined with a free-floating drifter that was deployed for 12–14 h. Production rates, averaged over the deployment time, were highest at or near the surface (ca. 2.4–3.5 nM h−1) and decreased rapidly with depth to 0.1–0.7 nM h−1 at 10–20 m. The decrease in production rates with depth generally paralleled the decrease in ultraviolet irradiance in the water column. Production rates of hydrogen peroxide in Antarctic seawater were largely controlled by the ultraviolet irradiance in the water column, although there was some evidence for production in the blue region of the solar spectrum. A laboratory study was conducted to determine the wavelength dependence of the apparent quantum yield for the photochemical formation of hydrogen peroxide in Antarctic waters. Apparent quantum yields determined at 0°C decreased from 0.74×10−3 mol einstein−1 at 290 nm to 1.0×10−5 mol einstein−1 410 nm. At 20°C, apparent quantum yields for the photochemical production of hydrogen peroxide were within a factor of two of apparent quantum yields determined in temperate waters at 20–25°C. Sunlight-normalized H2O2 production rates were determined as a function of wavelength using noontime irradiance data from Palmer Station, Antarctica. A decrease in stratospheric ozone from 336 to 151 Dobson units resulted in a predicted 19–42% increase in the photoproduction of H2O2 at the sea surface in Antarctic waters. The magnitude of this increase depends on the concentration and absorbance characteristics of dissolved organic matter in the photic zone, as well as on other factors such as cloudiness and decreasing solar zenith angle that tend to lower photochemical rates offsetting increases due to stratospheric ozone depletion.  相似文献   

8.
Denitrification, anammox (Anx) and di-nitrogen fixation were examined in two mangrove ecosystems- the anthropogenically influenced Divar and the relatively pristine Tuvem. Stratified sampling at 2 cm increments from 0 to 10 cm depth revealed denitrification as the main process of N2 production in mangrove sediments. At Divar, denitrification was ∼3 times higher than at Tuvem with maximum activity of 224.51 ± 6.63 nmol N2 g−1 h−1 at 0–2 cm. Denitrifying genes (nosZ) numbered up to 2 × 107 copies g−1 sediment and belonged to uncultured microorganisms clustering within Proteobacteria. Anammox was more prominent at deeper depths (8–10 cm) mainly in Divar with highest activity of 101.15 ± 87.73 nmol N2 g−1 h−1 which was 5 times higher than at Tuvem. Di-nitrogen fixation was detected only at Tuvem with a maximum of 12.47 ± 8.36 nmol N2 g−1 h−1. Thus, in these estuarine habitats prone to high nutrient input, N2-fixation is minimal and denitrification rather than Anx serves as an important mechanism for counteracting N loading.  相似文献   

9.
以黄海绿潮暴发的主要漂浮种类浒苔 (Ulva prolifera)为材料,在实验室条件下研究了浒苔光合参数、固碳速率及提升海水pH的作用,结果表明:浒苔光合作用半饱和常数Km为0.25 mmol/dm3,光合作用饱和时海水溶解无机碳(DIC)浓度也只需1.2 mmol/dm3,为正常海水DIC浓度(2.4 mmol/dm3)一半,故黄海绿潮暴发时藻体可以一直保持光合作用饱和与旺盛生长状态。水生条件下浒苔藻体主要吸收海水中的DIC,0.5 g/dm3培养密度下,1个光周期内净光合固碳速率为10.92 mg /(g·d)(鲜重)。连续培养5 d,0.5,1.0和2.5 g/dm3培养密度组的DIC浓度从22 mg/dm3分别降为4.85,2.62和0.66 mg/dm3,表明DIC去除率随藻体培养密度提高而增强,分别可达77.78%,88.00%,96.98%;藻体吸收海水中无机碳的同时可使海水pH升高,0.5 g/dm3培养密度下,1个光周期内净提升pH速率高达0.96/(dm3·g·d)。连续培养5 d,0.5,1.0和2.5 g/dm3培养密度组第1天其pH分别可达到9.1,9.2和9.7,表明藻体密度越高pH提升越快,而且第5天pH均可稳定在9.9左右。浒苔暴露在空气中可直接吸收空气中CO2,1个光周期内其光合固碳速率约为46.14 mg/(g·d),而在海水中的光合固碳速率为10.92 mg/(g·d),可见浒苔在空气中的光合固碳速率是水中的4.23倍。水生和气生时单位质量藻体的固碳效率因藻体间相互遮蔽而下降。结果可为今后黄海绿潮暴发机制及CO2减排和防止海洋酸化作用的评估提供技术支撑。  相似文献   

10.
This study aimed at establishing the trophic significance of the kelp Laminaria digitata for consumers inhabiting two rocky shores of Northern Brittany (France), displaying contrasted ecological conditions. The general trophic structure did not vary between these two sites, with a wide diversity of filter-feeders and predators, and only 14% of the species sampled belonging to the grazers' trophic group. The diversity of food sources fueling the food web appeared also similar. The food webs comprised four trophic levels and the prevalence of omnivory appeared relatively low compared to previous studies in the same area. Conversely, to the food web structure, which did not differ, the biochemical composition of L. digitata differed between the two sites, and was correlated to a larger diversity of grazers feeding on this kelp in sheltered conditions. This indicated that the spatial variability occurring in the nutritive value of L. digitata is likely to deeply affect the functioning of kelp-associated food webs. The contribution of L. digitata-derived organic matter to the diet of filter-feeders inhabiting these two environments was assessed using the mixing model Isosource, which showed the higher contribution of kelp matter in sheltered conditions. These results highlight the spatial variability that may occur in the functioning of kelp-associated food webs. Moreover, this suggests that hydrodynamics is likely to control the availability of kelp-derived organic matter to local filter-feeders, probably through an increase of detritus export in exposed areas.  相似文献   

11.
Highly sensitive STOX O2 sensors were used for determination of in situ O2 distribution in the eastern tropical north and south Pacific oxygen minimum zones (ETN/SP OMZs), as well as for laboratory determination of O2 uptake rates of water masses at various depths within these OMZs. Oxygen was generally below the detection limit (few nmol L−1) in the core of both OMZs, suggesting the presence of vast volumes of functionally anoxic waters in the eastern Pacific Ocean. Oxygen was often not detectable in the deep secondary chlorophyll maximum found at some locations, but other secondary maxima contained up to ~0.4 µmol L−1. Directly measured respiration rates were high in surface and subsurface oxic layers of the coastal waters, reaching values up to 85 nmol L−1 O2 h−1. Substantially lower values were found at the depths of the upper oxycline, where values varied from 2 to 33 nmol L−1 O2 h−1. Where secondary chlorophyll maxima were found the rates were higher than in the oxic water just above. Incubation times longer than 20 h, in the all-glass containers, resulted in highly increased respiration rates. Addition of amino acids to the water from the upper oxycline did not lead to a significant initial rise in respiration rate within the first 20 h, indicating that the measurement of respiration rates in oligotrophic Ocean water may not be severely affected by low levels of organic contamination during sampling. Our measurements indicate that aerobic metabolism proceeds efficiently at extremely low oxygen concentrations with apparent half-saturation concentrations (Km values) ranging from about 10 to about 200 nmol L−1.  相似文献   

12.
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   

13.
The life-histories and the secondary production of four dominant peracarid crustaceans (the mysids Boreomysis arctica and Parapseudomma calloplura, the amphipod Rhachotropis caeca, and the isopod Ilyarachna longicornis) in bathyal depths of the Bay of Biscay (NE Atlantic; between 383 and 420 m) and the Catalan Sea (Northwestern Mediterranean; between 389 and 1355 m) were established. Both the Atlantic and the Mediterranean populations of the major part of the target-species had two generations/year with mean cohort-production intervals (CPI) ranging from 5.5 mo for Ilyarachna longicornis to 6.3 mo for Parapseudomma calloplura. The Hynes method showed secondary production to vary in the Bay of Biscay between 0.113 mg DW m−2 yr−1 for I. longirostris and 3.069 mg DW m−2 yr−1 for P. calloplura, with P/B ratios between 4.57 (I. longirostris) and 7.93 (Boreomysis arctica). In the Catalan Sea, production varied between 0.286 mg DW m−2 yr−1 for I. longirostris and 1.096 mg DW m−2 yr−1 for P. calloplura, with P/B between 5.72 (I. longirostris) and 6.66 (P. calloplura). Application of two different empiric models to the whole peracarid assemblage gave similar levels of secondary production in both study areas (between 29.26 and 32.14 mgDWm−2 yr−1 in the Bay of Biscay; between 26.23 and 26.54 mg DW m−2 yr−1 in the Catalan Sea). From the analysis of gut contents of 22 species the dominant species in each study area were assigned to two basic trophic levels, detritus feeders and predators. Also, cumulative curves of dominance showed high diversity (low dominance) for peracarid assemblages distributed at mid-bathyal depths (524–693 m) both in the Bay of Biscay off Arcachon and in the Catalan Sea off Barcelona. We also discuss and compare, both within and between areas, how environmental features may explain the observed diversity patterns, the trophic structure, and the production results obtained for the suprabenthos assemblages.  相似文献   

14.
The oxidation and reduction of nanomolar levels of copper in air-saturated seawater and NaCl solutions has been measured as a function of pH (7.17–8.49), temperature (5–35 °C) and ionic strength (0.1–0.7 M). The oxidation rates were fitted to an equation valid at different pH and ionic strength conditions in sodium chloride and seawater solutions:
The reduction of Cu(II) was studied in both media for different initial concentrations of copper(II). When the initial Cu(II) concentration was 200 nM, the copper(I) productions were 20% and 9% for NaCl and seawater, respectively. The effect of speciation of copper(I) reduced from Cu(II) on the rates was studied. The Cu(I) speciation is dominated by the CuCl2− species. On the other hand, the neutral chloride CuCl species dominates the Cu(I) oxidation in the range of 0.1 M to 0.7 M chloride concentrations.  相似文献   

15.
《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   

16.
The precision of spectrophotometric measurements of indicator absorbance ratios is sufficient to allow evaluation of small isotopically induced differences in the dissociation constant of boric acid (KB). The quotient of 11KB and 10KB, obtained using isotopically ⩾99% pure borate/boric acid buffers, provides an equilibrium constant for the reaction 10B(OH)3+11B(OH)4−⇔11B(OH)3+10B(OH)4− which heretofore had not been experimentally determined. Previous theoretical and semi-empirical evaluations of this equilibrium, which is important for assessments of the paleo-pH of seawater and the paleo-pCO2 of the atmosphere, have yielded constants, 11–10KB=10KB/11KB, that have ranged between 1.0194 and approximately 1.033. The experimentally determined value 11–10KB=1.0285±0.0016 (mean±95% confidence interval) obtained at 25 °C and 0.63 molal (mol kg−1 H2O) ionic strength is in much better agreement with recent theoretical assessments of 11–10KB that have ranged between 1.026 and 1.033, than the much-cited original estimate (1.0194) of Kakihana et al. (1977) [Fundamental studies on the ion-exchange separation of boron isotopes. Bulletin of Chemical Society of Japan 50, 158–163]. Since the activity quotient for the fractionation reaction is almost equal to unity, it is expected that the 11–10KB value obtained in this study will be applicable over a wide range of solution compositions and ionic strengths.  相似文献   

17.
We studied the seasonal, diel, and vertical distribution of phytoplankton N2 fixation to understand the relative contributions of unicellular and filamentous nitrogen fixers (diazotrophs) to N2 fixation and nitrogen recycling in the northern South China Sea (SCS) and the neighboring upstream Kuroshio. N2-fixation rates were measured by the 15N2 tracer technique (addition by bubble) on unicellular (<10 or 20 µm) and the filamentous diazotrophs (>10 or 20 µm, mostly Trichodesmium and Richelia) fractionated by 10- or 20-µm mesh sizes. The mean depth-integrated total (unicellular+filamentous) N2-fixation rates in the SCS (51.7±6.2 µmol N m−2 d−1) averaged 1/3 of that in the Kuroshio (142.7±29.6 µmol N m−2 d−1), with higher rates in the winter than in other seasons in the SCS and the opposite seasonal pattern in the Kuroshio. Unicellular diazotrophs contributed 65% of the total N2 fixation in the SCS, which were negatively correlated with surface temperature and, as for total N2 fixation, were higher in the winter when Trichodesmium spp. were scarce. In comparison, the unicellular diazotrophs contributed 50% of total N2 fixation in the Kuroshio, and their contributions were not significantly correlated with surface temperature. In both the SCS and the Kuroshio, the unicellular N2 fixation was more important during the night than during the day, and in the deep euphotic layer than in the surface layer, even in the daytime. Our results show that the unicellular diazotrophs were important N2 fixers and contributed significantly to N2 fixation in the tropical marginal seas, more so in the SCS than the Kuroshio.  相似文献   

18.
日本真海带对硒的积累和生物转化   总被引：4，自引：0，他引：4  
在海水中添加亚硒酸盐(Na2SeO3)及不同浓度的氮磷营养盐(NaNO3+NaHO2PO4),研究海带对硒的积累,通过分离测定海带富硒前后各生化组分的含硒量来探讨硒的生物转化问题.结果表明天然海带含硒量(鲜重)为0.451~0.596μg/g,海带富硒最佳的Na2SeO3浓度为200mg/dm3,培养56h后的富硒倍率约为50.在天然海带中,硒主要以有机态存在,有机硒占总硒含量的86.22%;在含有200mg/dm3NaO2SeO3的海水中培养56h后测得海带的总硒为24.481μg/g,其中有机硒含量为16.703μg/g,无机硒为4.714μg/g;在添加氮磷营养盐的含硒海水中,海带的富硒能力得到进一步的提高,在适宜的氮磷条件下(150mg/dm3NaNO3和25mg/dm3NaHO2PO4)总硒含量达到33.649μg/g,而无机硒含量基本不变,为4.497μg/g,因此提高部分转化为有机硒,有机硒含量达到24.678μg/g.这说明海带具有通过自身代谢将无机硒转化为有机硒的较强的能力.  相似文献   

19.
The bivalve molluscs Mytilus californianus and Crassostrea gigas were exposed to filtered seawater containing the isotope 95mTc added as pertechnetate (TcO4?) to study the biokinetic behaviour of this element. Whole body concentration factors for both organisms at equilibrium were small (CF = 1·3–1·5); individual organ concentration factors were highest for the visceral mass in both. Loss rates determined both in the laboratory and under field conditions were biphasic for both molluscs; initial loss of Tc was rapid with slightly more than 50 % of the initial label being lost within 10 days. Thereafter, loss rates decreased and whole body biological half-lives ranged from 80 to 134 days. Neither I? nor IO3? affected the uptake of Tc by M. californianus even when concentrations of these anions exceeded those normally present in seawater by two orders of magnitude.  相似文献   

20.
《Marine Chemistry》2007,103(1-2):1-14
We succeeded in determining the Ce isotopic composition (138Ce/142Ce) in seawater with an error of 2σm = 0.3–0.7 of ε unit. In this study, 1000–3000 L of seawater samples were passed through MnO2 fibers to concentrate Ce and Nd for precise measurement of their isotope ratios. Four surface seawater samples of the northwestern Pacific and a coastal sample in Tokyo Bay were analyzed. Most Ce isotope ratios in the surface water showed positive εCe values (+ 0.8 to + 1.4) in the northwestern Pacific Ocean. These values indicate that Ce in the surface water originates from the continental crust preferentially over mantle-derived materials. We examined binary mixing model between the continental crust and mid-ocean ridge basalt. However the model could not explain both isotopic compositions and concentrations, which implies that the atmospheric input was a possible pathway for Ce into the ocean. A negative εCe value was observed in Tokyo Bay, suggesting mantle-derived sources.  相似文献   

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