首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 31 毫秒
1.
A high sensitivity manifold for the determination of trace quantities (nanomolar concentrations) of nitrate+nitrite and nitrite alone is described. The method uses a classical Technicon AutoAnalyzer II usually employed for shipboard analysis. A reproducibility of ± 1 nmol dm−3 for nitrate plus nitrite and nitrite alone was obtained, with an analytical rate of 40 samples h−1.  相似文献   

2.
The vestimentiferan tubeworm Riftia pachyptila derives most or all of its nutrition from intracellular chemosynthetic bacterial symbionts. Because purified preparations of symbionts respire nitrate, possibly nitrite, and oxygen, host transport of nitrate is a topic of interest. In the present study, we have developed a nitrate detection assay that utilizes a nitrite reductase-deficient Escherichia coli strain for the reduction of nitrate to nitrite, which is then determined spectrophotometrically. Nitrate and nitrite concentrations were measured in the blood and coelomic fluids of R. pachyptila collected from hydrothermal vent sites at 9°N and 13°N. The blood was shown to have nitrate concentrations up to one hundred times that of ambient sea water (40 μM). Blood nitrate levels reached concentrations of>1 mM, while nitrite was measured in the range of 400-700 μM. The concentrations of nitrate and nitrite in the coelomic fluids were 150-240 μM and <20 μM, respectively. The nitrate determination technique we present here is simple, applicable for laboratory and shipboard use on sea water or biological fluids, and works reliably within the 0.5 to 2000 μM range.  相似文献   

3.
We developed a simple and reliable method which allows simultaneous determination of organic forms of carbon (DOC), nitrogen (DON) and phosphorus (DOP) dissolved in seawater. Conversion of dissolved organic matter (DOM) to inorganic products (carbon dioxide, nitrate+nitrite and soluble reactive phosphate) is performed by a persulfate wet-oxidation in low alkaline condition. After oxidation, the concentration of the inorganic products dissolved in the sample was measured automatically by colorimetry using a 3-channel Technicon AutoAnalyzer system. A number of pure organic compounds were tested in the concentration range encountered in coastal and open ocean, indicating a high efficiency of the digestion procedure. The recovery range is similar to that obtained by other wet-oxidation procedures and by high-temperature catalytic oxidation techniques. Direct comparisons with usual methods used for separate determination of DOC, DON and DOP indicated a high efficiency of the procedure. Reproducibility tests demonstrated a very good precision (around 5%) for lagoonal and coastal waters, while precision was sometimes around 10–25% in oligotrophic oceanic waters, especially for DOP where values approached limits of detection for measuring phosphate. This method is highly suitable for routine analysis and especially appropriate for shipboard work.  相似文献   

4.
A highly sensitive laser-induced fluorescence (LIF) system has been developed to study the fluorescence of dissolved organic carbon (DOC) in the marine environment. The LIF detector has a detection limit of 10 attomoles (10 × 10−18 moles) of pterin and eliminates internal quenching in highly fluorescent samples such as anoxic porewaters encountered when using conventional fluorometry. LIF analysis is rapid, reproducible, and uses only 100 μl of a sample. This small size requirement permits fluorescence analyses of samples often available only in limited amounts, such as porewaters, hydrothermal vent waters, and rainwaters. In addition, the LIF detection system may greatly simplify extraction and separation procedures required to characterize the fluorescent components of DOC.  相似文献   

5.
传统分光光度法测定硝酸盐和亚硝酸盐含量时检测限较高,无法测定部分海洋表层及寡营养盐海域低含量的硝酸盐和亚硝酸盐浓度,急需采用一种新的测定低浓度硝酸盐和亚硝酸盐的方法.化学发光法用于测定水体中硝酸盐和亚硝酸盐含量,具有灵敏度高、检测限低、样品用量少,不受悬浮颗粒物、有色物质影响及样品批量测定等优点.本文通过探索载气流速、...  相似文献   

6.
A chemiluminescent analysis technique for the determination of nanomolar quantities of nitrate, nitrate plus nitrite or nitrite alone in seawater is described. The method depends on the selective reduction of these species to nitric oxide which is then determined by its chemiluminescent reaction with ozone, using a commercial nitrogen oxides analyzer. The necessary equipment is compact and sufficiently sturdy to allow shipboard use. A precision of ±2 nM is claimed with analytical rates of 10–12 samples h?1, and modifications are discussed to allow doubling the analytical rate.  相似文献   

7.
Uptake rates of ammonium, nitrate, urea and nitrite were measured for 1 year (1988) at a coastal station in the well-mixed waters of the western English Channel. Ammonium was the major form of nitrogen (N) utilized (48%) by phytoplankton, followed by nitrate (32%), urea (13%) and nitrite (7%). Seasonal changes of uptake of ammonium, nitrate and urea showed a broad, intense summer maximum. Nitrite uptake was low throughout the year except for a peak value in June. Uptake rates of ammonium and nitrate were independent of substrate concentrations, whereas those of urea and nitrite were not. The summer maxima of ammonium, nitrate and total N uptake, and the significant relationships of N-uptake index to ambient light, and of chlorophyll-a-specific N uptake to surface-incident light, indicate that light is the major factor controlling N uptake in these waters. This is due to the permanent vertical mixing which reduces the mean light available for N uptake to <15% of the incident light. Mixing also injects regenerated N continuously into the euphotic zone, thus alleviating nitrogen limitation and accounting for the larger proportion of regenerated N uptake in total N uptake.  相似文献   

8.
The influence of the Columbia River plume on the distributions of nitrate and iron and their sources to coastal and shelf waters were examined. In contrast to other large estuaries, the Columbia River is a unique study area as it supplies very little nitrate (5 μM) and iron (14–30 nM) at salinities of 1–2 to coastal waters. Elevated nitrate and dissolved iron concentrations (as high as 20 μM and 20 nM) were observed, however, in the near field Columbia River plume at salinities of 20. Surface nitrate concentrations were higher than observed in the Columbia River itself and therefore must be added by entrainment of higher nitrate concentrations from subsurface coastal waters. Tidal flow was identified as an important factor in determining the chemical constituents of the Columbia River plume. During the rising flood tide, nitrate and iron were entrained into the plume waters resulting in concentrations of 15 μM and 6 nM, respectively. Conversely, during the ebb tide the concentrations of nitrate and total dissolved iron were reduced to 0.3–3 μM and 1–2 nM, respectively, with a concomitant increase in chlorophyll a concentrations. As these plume waters moved offshore the plume drifted directly westward, over a nitrate depleted water mass (< 0.2 μM). The plume water was also identified to move southwards and offshore during upwelling conditions and nitrate concentrations in this far field plume were also depleted. Iron concentrations in the near-field Columbia River plume are sufficient to meet the biological demand. However, due to the low nitrate in the Columbia River itself, nitrate in the plume is primarily dependent on mixing with nitrate rich, cold, high salinity subsurface waters. Without such an additional source the plume rapidly becomes nitrate limited.  相似文献   

9.
The method of Parsonset al. (1984) for measuring dissolved free amino acids (DFAA) in coastal seawater was modified. We found considerable interference in DFAA determination from ammonia dissolved in coastal seawater, although the interference of urea could be ignored. For DFAA analysis for coastal seawater samples, ammonia determinations for the same sample are needed to correct DFAA values. For coastal surface seawater samples from all over the Seto Inland Sea, Japan, values of DFAA ranged from undetectable to 1.87 μg-at N/l when corrected for ammonia, while uncorrected values ranged from undetectable to 2.61 μg-at N/l. DFAA, urea, nitrate+nitrite, ammonia and DON concentrations in surface seawater collected in the Seto Inland Sea were analyzed simultaneously. DFAA at four seasons constituted from 1.4 to 10.1% of DON, with a mean value of 6.5%. The concentration of urea was similar to that of DFAA and often higher than that of ammonium, although generally lower than that of nitrate.  相似文献   

10.
Fine scale distribution of nitrous oxide in marine sediments   总被引：1，自引：0，他引：1  
Vertical profiles of nitrous oxide and other inorganic nitrogen compounds in the sediments in Tokyo Bay and its vicinity were measured using the whole core squeezing method. Within the bay area, vertical profiles of nitrous oxide in the interstitial waters showed one or two distinctive peaks around the depth of 2–4 cm, which corresponded to the peaks of nitrite and nitrate. In situ formation of nitrous oxide through nitrification was suggested in those sediments, which was possibly activated by the presence of benthic animals. On the other hand, at the deep sediment off Tokyo Bay the profiles of nitrous oxide, nitrite and nitrate gave a monotonous single peak, indicating less bioturbated condition. Denitrification or dissimilatory nitrate reduction might be important for the formation of nitrous oxide peaks in the latter type of sediment.  相似文献   

11.
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   

12.
Sediment samples ranging from 0.05 to 278 m below sea floor (mbsf) at a Northwest Pacific deep-water (5564 mbsl) site (ODP Leg 191, Site 1179) were analyzed for phospholipid fatty acids (PLFAs). Total PLFA concentrations decreased by a factor of three over the first meter of sediment and then decreased at a slower rate to approximately 30 mbsf. The sharp decrease over the first meter corresponds to the depth of nitrate and Mn(IV) reduction as indicated by pore water chemistry. PLFA-based cell numbers at site 1179 had a similar depth profile as that for Acridine orange direct cell counts previously made on ODP site 1149 sediments which have a similar water depth and lithology. The mole percentage of straight chain saturated PLFAs increases with depth, with a large shift between the 0.95 and 3.95 mbsf samples. PLFA stable carbon isotope ratios were determined for sediments from 0.05 to 4.53 mbsf and showed a general trend toward more depleted δ13C values with depth. Both of these observations may indicate a shift in the bacterial community with depth across the different redox zones inferred from pore water chemistry data. The PLFA 10me16:0, which has been attributed to the bacterial genera Desulfobacter in many marine sediments, showed the greatest isotopic depletion, decreasing from − 20 to − 35‰ over the first meter of sediment. Pore water chemistry suggested that sulfate reduction was absent or minimal over this same sediment interval. However, 10me16:0 has been shown to be produced by recently discovered anaerobic ammonium oxidizing (anammox) bacteria which are known chemoautotrophs. The increasing depletion in δ13C of 10me16:0 with the unusually lower concentration of ammonium and linear decrease of nitrate concentration is consistent with a scenario of anammox bacteria mediating the oxidation of ammonium via nitrite, an intermediate of nitrate reduction.  相似文献   

13.
Dissolved organic nitrogen (DON), dissolved organic carbon (DOC) and inorganic nutrient concentrations were determined in samples from an area encompassing the Northeast Water Polynya from June to August 1993. In June, still ice-covered polynya area surface waters (PySW) had significantly higher (p<0.05) DOC concentrations (110 μM, n=68) than surface water outside the polynya area (96 μM, n=6). Melting ice and ice algae are suggested as DOC sources. DOC concentrations found in this study are consistent with other studies showing higher DOC concentrations in the Arctic than in other ocean areas. As the productive season progressed, DOC concentrations in Polynya surface water (PySW) decreased (p<0.05) from 110 to 105 μM, while DON concentrations increased (p<0.05) from 5.6 to 6.1 μM, causing a significant decrease (p<0.05) in the C : N ratios of DOM from spring (C : N ratio 20) to summer (C : N ratio 17). We found a significant (p<0.05) decrease in the DOM C : N ratio in all water masses within the polynya area as the productive season progressed. DON was the largest fraction of total dissolved nitrogen (TDN) in PySW and surface waters outside the polynya area. TDN was calculated as the sum of DON, nitrate, nitrite and ammonium concentrations. DON increased (p<0.05) from 62% to 73% of TDN in PySW from spring to summer, a result of increasing DON concentrations and decreasing inorganic nitrogen concentrations over the productive season. The seasonal accumulation of DON and the corresponding decrease in nitrate concentrations in waters with primary production indicate that it is important to take the DON pool into account when estimating export production from nitrate concentration decreases in surface waters. PySW TDN concentrations decreased (p<0.05) from 9.1 (n=61) to 8.6 μM (n=60) from spring (May 25 through June 19) to summer (July 1 through July 27). The seasonal decrease in surface water TDN concentrations corresponded to increases in TDN concentrations in deeper water masses within the Polynya. Most of the TDN increase in deep water was in the form of DON. A possible explanation is that PON was dissolved (partially remineralized) in the water column at mid depths, causing increases in the DON concentration. Transfer of N from PySW (with a short residence time in the polynya area) to Polynya Intermediate Water and deep waters of the Norske and Westwind Trough with multi-year residence times keeps N from leaving the polynya area. In spring, nutrients from degradation of OM in PyIW could support primary production. The role of PyIW as an OM trap could be important in supporting primary production in the polynya area.  相似文献   

14.
1 Indroduction The coastal zone and continental shelf area is an important region in the global biogeochemical cycle of nutrients in the ocean. This portion of the global ocean interacts closely with the continents, atmosphere and the open ocean in a comp…  相似文献   

15.
Macrofauna, nutrient fluxes, porewater chemistry and sediment characteristics were measured at six intertidal mudflat sites in the Humber Estuary, U.K., during the different seasons. Nereis diversicolor , Macoma balthica and Corophium volutator were found to be the dominant macrofauna. Salinity was the baseline control on macrofauna distribution but this was overprinted by periodic impoverishment due to sediment mobilization. High resolution gel probe porewater samplers provided direct evidence for the impact of burrows on porewater chemistry. The macrofauna modified nutrient fluxes during periods of mud flat stability. Nereis caused a decrease in silicate and phosphate effluxes but enhanced ammonia release and nitrate uptake. Macoma enhanced ammonia and nitrite release. The impact of Corophium was not possible to discern. The Humber is a large, highly dynamic macrotidal estuary in which sediment resuspension has a large impact on porewater profiles, nutrient fluxes and macrofaunal communities. Simple patterns and inter-relationships which are seen in small sheltered estuaries are not observed in the Humber.  相似文献   

16.
Photochemical production rates and steady-state concentrations of the highly reactive OH radical were determined in Antarctic seawater in the Weddell-Scotia Confluence during the austral spring of 1993 and along the Antarctic Peninsula during the austral summer of 1994. OH radical photoproduction rates were 30±2 nM/day and 46±2 nM/day in surface open oceanic and coastal waters, respectively. Corresponding steady-state concentrations were 2.6×10−19 and 4.3×10−19 M which are similar to those found in tropical latitudes. In-situ irradiation experiments (drifter deployments) at different depths in the upper water column indicated that multiple sources for the OH radical existed at three Antarctic stations. Ultrafiltration studies and model calculations based on wavelength-dependent OH radical quantum yields indicated that the main sources were photochemical reactions of low molecular weight dissolved organic matter (DOM), nitrate, and nitrite. Production of the OH radical from nitrate photolysis was almost exclusively UV-B dependent, while OH radical production from nitrite photolysis was mainly UV-A dependent. OH production from DOM photolysis was both UV-A and UV-B dependent. In the upper few meters at open oceanic sites, nitrate and DOM were the dominant OH radical sources, while deeper in the water column DOM and nitrite were important because of the greater importance of UV-A with depth. During non-ozone hole conditions, nitrate contributed about 33%, while DOM plus nitrite contributed about 67% of the predicted OH radical production in open oceanic surface waters. During an ozone hole (151 Dobson units), the corresponding percentages changed to about 40 and 60% for nitrate and DOM due to the higher UV-B irradiance. Model calculations predict that during an ozone hole (151 Dobson units), OH radical production in surface waters will be enhanced by at least 20%, mostly from nitrate photolysis and to a lesser extent from DOM photochemical reactions. This study indicates that ozone hole events significantly increase OH radical production, as well as the photolysis of DOM, in Antarctic waters, and that rates can be as high or higher than those at lower latitudes, especially if differences in temperature and solar irradiance are taken into account.  相似文献   

17.
The unstable state of nitrite results in its very low concentration in seawater,which is below the limit of detection(LOD) of conventional techniques of analysis. Some sensitivity-enhanced methods have been proposed for the determination of nitrite at nanomolar level to illustrate the role of nitrite in the marine nitrogen cycle. However,most of previous reports are not widely accepted,because of their complexity and cost equipment or intensive labor requirement. In this study,a simple automatic system for the determination of nanomolar level nitrite using on-line preconcentration with spectrophotometric detection was described. An Oasis HLB cartridge was adopted to quantitatively enrich the pink-colored azo compound,formed from nitrite via Griess reaction. The cartridge was rinsed with water and ethanol(volume fraction is 55%,the same below) ,in turn,then eluted by an eluent containing 50% ethanol and 0.25 M(mol/dm 3 ) H 2 SO 4,and determined at 543 nm with a 2 cm path-length flow cell. Under the optimized experimental conditions,the calibration curve showed a good linearity in the range of 1.4-85.7 nM,and the LOD(3σ) was estimated to be 0.5 nM. The relative standard deviations of 7 measurements were 4.0% and 1.0% for the samples spiked at 7.1 and 28.6 nM,respectively. The recoveries for the different natural water samples were between 92.2%-108.4%. Each HLB cartridge could be reused for at least 50 times. As compared with other SPE methods,the advantages of this method included the free of interference from salinity variation and less sample consuming. The results of the application of the proposed method to natural water showed good agreement with liquid waveguide capillary cell detection method.  相似文献   

18.
Surface temperature, salinity, concentrations of silicate (Si) and nitrate + nitrite (N), and in vivo fluorescence (Fluor) were investigated in the marginal ice zone (MIZ) and the seasonally open oceanic zone (SOOZ) (32–40°E, 64–69°S) from February 23 to 28 1992. In the MIZ the mean Si and N were 67.8 ± 2.2 M and 32.5 ± 1.7 M, respectively. There was a trend that low N values coincided with high Fluor values. Observation conducted at one point (64°S, 38°E) revealed a diel variation pattern in Fluor. Applying this pattern of deviation from noon value, all Fluor data were normalized to value at local noon. In the MIZ a significant negative correlation was observed between the normalized Fluor and N but not Si. On the other hand, Si decreased continuously from south to north in the SOOZ and was negatively correlated with the normalized Fluor. Difference in Si concentration was about 30 M between the sea around 64°S and the MIZ, while the difference in N concentration was estimated as less than 10 M. If diatoms take up silicate and nitrogen at an approximate ratio of 1:1, additional nitrogenous nutrients other than nitrate and nitrite (e.g. ammonia, urea etc.) would be required. In this case, an f-ratio of lower than 33% is obtained. It is suggested that in the MIZ abundance of phytoplankton community dominated by non-diatom increases utilizing nitrate while in the SOOZ abundance of phytoplankton community dominated by diatoms increases consuming Si and regenerated nitrogen.  相似文献   

19.
Jian Ma  Dongxing Yuan  Ying Liang   《Marine Chemistry》2008,111(3-4):151-159
A cartridge of solid phase extraction (SPE), hydrophilic–lipophilic balance (HLB), has been used to enrich phosphomolybdenum blue (PMB) from water samples without any other additives. Based on this, the previous on-line SPE method established for the determination of nanomolar soluble reactive phosphorus (SRP) in seawater has been greatly improved. Cetyltrimethylammonium bromide (CTAB), the cationic surfactant needed for the formation of the PMB-CTAB paired compound that could be extracted on a Sep-Pak C18 cartridge using the previous method [Liang, Y., Yuan, D.X., Li, Q.L., Lin, Q.M., 2007. Flow injection analysis of nanomolar level orthophosphate in seawater with solid phase enrichment and colorimetric detection. Marine Chemistry 103, 122–130.], was not necessary. Thus the longer time and higher temperature required for the complete formation of the PMB-CTAB compound were no longer needed. In addition, with application of the sequential injection analysis technique the proposed method showed the advantages of being much faster, simpler, sample and reagent saving, as well as more convenient in operation. The PMB compound formed under room temperature was efficiently extracted on an in-line HLB cartridge, rapidly eluted by 0.15 mol/L NaOH solution, and finally determined with a laboratory-made spectrophotometer at 740 nm. Experimental parameters, including the volume of reagents added, sample loading flow rate, and eluting flow rate, were optimized. Time and temperature for the PMB reaction, and salinity effect were also studied, and these were found to have no severe effect on the detection. With variation of sample loading time at a fixed flow rate, a broadened determination range of 3.4 to 1134 nmol/L phosphate could be obtained. The recovery and the method detection limit of the proposed method were found to be 94.4% and 1.4 nmol/L, respectively. The relative standard deviation (n = 7) was 2.50% for the sample at a concentration of 31 nmol/L phosphate. Two typical seawater samples were analyzed with both the proposed method and the magnesium hydroxide-induced coprecipitation method and, using the t-test, the results of the two methods showed no significant difference.  相似文献   

20.
叶绿素荧光遥感算法为探测近岸海域二类水体叶绿素浓度开辟了新途径．基于大连湾及邻近海域的实测数据,本文研究了海水叶绿素浓度的荧光遥感算法．结果表明：随着海水叶绿素质量浓度的增高,荧光峰出现显著的红移现象,叶绿素质量浓度与荧光峰波长存在着正相关关系．此外,基于MODIS、MERIS及GLI传感器荧光波段建立的荧光基线高度算法较差,不适用于该研究海域．选择680、685、690、695、700、705nm作为荧光峰波长建立的荧光基线高度算法,随着选定波长的增大,该算法拟合的相关性逐渐增高,最大相关系数（R2）可达0．91;而以实测荧光峰波长建立的荧光基线高度算法最佳,乘幂函数拟合优于线性拟合,拟合方程为P（chl）=3．167×10^5 FLH^1.45（R2=0．93）．本研究为新一代海洋水色卫星传感器的开发、建造提供了科学依据,并为已有高光谱传感器在叶绿素荧光遥感反演方面的应用打下了基础．  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号