海水中沉底油的风化特性及鉴别方法研究

通过对具有代表性的两种原油和两种船用燃油进行340 d的室外模拟风化模拟实验,运用GC-FID法和同步荧光光谱法对海水中风化的漂浮油和沉底油的特性进行分析,为沉底油溯源提供相关依据,以此完善海上溢油事故的监管工作。结果表明:4种实验油品的漂浮油和沉底油荧光光谱差别不大,因此可以用荧光光谱法初步测定沉底油的风化时间;沉底油受蒸发、光解等影响弱于漂浮油,其GC可保持低碳组分峰形,并且由于生物降解,沉底油的气相谱图中均出现不可分辨的复杂混合物(UCM)的特征图谱,可以作为判断是否沉底的判据;两种方法相结合,可以建立一种确定溢油时间、风化经历及方法,以便对溢油进行更准确的溯源。     

天然海水硝酸盐氮同位素组成的蒸馏法测定

建立了测定天然海水中硝酸盐氮同位素组成的蒸馏法,该方法主要是在碱性条件下利用戴氏合金将海水中的硝酸盐还原为氨,后利用稀盐酸吸收生产的氨,将得到的氨吸收液浓缩后干燥结晶,利用同位素比值质谱仪测定所得晶体的氮同位素组成。研究中开展了戴氏合金添加量及氨吸收溶液在不同条件下干燥结晶对氮同位素测值的影响研究。结果表明,戴氏合金添加量为3.0 g及60 ℃下直接干燥结晶为最佳的实验条件。所建立的氨蒸馏法氮空白值仅为(0.90±0.19) μmol,低于此前文献报道的氮空白值;氮同位素组成(δ15N)空白值为(-14.7±4.1)×10-3。运用所建立的氨蒸馏法实测得到的硝酸盐δ15N值与氨扩散法、硝酸盐直接测定法得到的数值非常吻合,进一步证明所建立氨蒸馏法的可靠性。改进后的氨蒸馏法适用于硝酸盐浓度在2~50 μmol/dm3内的天然海水硝酸盐氮同位素组成的测定,方法的标准偏差为±0.3×10-3。     

Winkler's method overestimates dissolved oxygen in seawater: Iodate interference and its oceanographic implications

Dissolved oxygen in seawater has been determined by using the Winkler's reaction scheme for decades. An interference in this reaction scheme that has been heretofore overlooked is the presence of naturally occurring iodate in seawater. Each mole of iodate can result in an apparent presence of 1.5 mol of dissolved oxygen. At the concentrations of iodate in the surface and deep open ocean, it can lead to an overestimation of 0.52 ± 0.15 and 0.63 ± 0.05 μmol kg^− 1 of oxygen in these waters respectively. In coastal and inshore waters, the effect is less predictable as the concentration of iodate is more variable. The solubility of oxygen in seawater was likely overestimated in data sources that were based on the Winkler's reaction scheme for the determination of oxygen. The solubility equation of García and Gordon [Garcia H.E., Gordon, L.I., 1992. Oxygen solubility in seawater: Better fitting equations. Limnol. Oceanogr. 37, 1307–1312] derived from the results of Benson and Krause [Benson, F.B., Krause, D. Jr., 1984. The concentration and isotopic fractionation of oxygen dissolved in freshwater and seawater in equilibrium with the atmosphere. Limnol. Oceanogr. 29, 620–632] is free from this source of error and is recommended for general use. By neglecting the presence of iodate, the average global super-saturation of oxygen in the surface oceans and the corresponding efflux of oxygen to the atmosphere both have been overestimated by about 8%. Regionally, in areas where the degree of super-saturation or under-saturation of oxygen in the surface water is small, such as in the tropical oceans, the net air–sea exchange flux can be grossly under- or overestimated. Even the estimated direction of the exchange can be reversed. Furthermore, the presence of iodate can lead to an overestimation of the saturation anomaly of oxygen in the upper ocean attributed to biological production by 0.23 ± 0.07%. AOU may have been underestimated by 0.52 ± 0.15 and 0.63 ± 0.05 μmol kg^− 1 in the surface mixed layer and deep water, while preformed phosphate and preformed nitrate may have been overestimated by 0.004 ± 0.001 and 0.06 ± 0.02 μmol kg^− 1 in the surface mixed layer, and 0.005 ± 0.0004 and 0.073 ± 0.006 μmol kg^− 1 in the deep water. These are small but not negligible corrections, especially in areas where the values of these parameters are small. At the increasing level of sophistication in the interpretation of oxygen data, this source of error should now be taken into account. Nevertheless, in order to avoid confusion, an internationally accepted standard needs to be adopted before these corrections can be applied.     

Trophic ecology and vertical patterns of carbon and nitrogen stable isotopes in zooplankton from oxygen minimum zone regions

The unique physical and biogeochemical characteristics of oxygen minimum zones (OMZs) influence plankton ecology, including zooplankton trophic webs. Using carbon and nitrogen stable isotopes, this study examined zooplankton trophic webs in the Eastern Tropical North Pacific (ETNP) OMZ. δ¹³C values were used to indicate zooplankton food sources, and δ¹⁵N values were used to indicate zooplankton trophic position and nitrogen cycle pathways. Vertically stratified MOCNESS net tows collected zooplankton from 0 to 1000 m at two stations along a north-south transect in the ETNP during 2007 and 2008, the Tehuantepec Bowl and the Costa Rica Dome. Zooplankton samples were separated into four size fractions for stable isotope analyses. Particulate organic matter (POM), assumed to represent a primary food source for zooplankton, was collected with McLane large volume in situ pumps.The isotopic composition and trophic ecology of the ETNP zooplankton community had distinct spatial and vertical patterns influenced by OMZ structure. The most pronounced vertical isotope gradients occurred near the upper and lower OMZ oxyclines. Material with lower δ¹³C values was apparently produced in the upper oxycline, possibly by chemoautotrophic microbes, and was subsequently consumed by zooplankton. Between-station differences in δ¹⁵N values suggested that different nitrogen cycle processes were dominant at the two locations, which influenced the isotopic characteristics of the zooplankton community. A strong depth gradient in zooplankton δ¹⁵N values in the lower oxycline suggested an increase in trophic cycling just below the core of the OMZ. Shallow POM (0–110 m) was likely the most important food source for mixed layer, upper oxycline, and OMZ core zooplankton, while deep POM was an important food source for most lower oxycline zooplankton (except for samples dominated by the seasonally migrating copepod Eucalanus inermis). There was no consistent isotopic progression among the four zooplankton size classes for these bulk mixed assemblage samples, implying overlapping trophic webs within the total size range considered.     

A catalytic oxidation method for the determination of total nitrogen dissolved in seawater

A detailed examination of a high-temperature catalytic oxidation method for liquid samples in the analysis of total nitrogen dissolved in seawater is reported. The nitrogenous compounds in liquid samples are oxidized on a platinum catalyzer at 680°C under oxygen atmosphere and the generated NO₂ is absorbed into a chromogenic reagent, followed by a spectrophotometric determination. The results of this method are much higher than those of wet oxidation methods. Molecular size dependency of the results clearly indicates that the above discrepancy is caused by the low oxidation capacity of the wet oxidation method against high-polymer organic matter dissolved in seawater. The results revealed that the concentration of total nitrogen in seawater is nearly constant from surface to bottom, ranging from 30 to 40 μM 1^?1, which organic nitrogen concentration higher in the surface layer, and a rapid decrease with depth. An examination of molecular size distribution indicates that the concentration of high-polymer organic nitrogen decreases rapidly from surface to deeper layers, with molecular sizes ranging from 5 × 10³ to 3 × 10⁴. Because of the well-defined principle of the oxidation process, its reliability, ease of sample handling and of analytical procedure on board or in the land laboratory, the present method is much more suitable for the marine analytical chemistry of total and organic nitrogen than the other previous methods.     

Oxygen distribution and aerobic respiration in the north and south eastern tropical Pacific oxygen minimum zones

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 (K_m values) ranging from about 10 to about 200 nmol L⁻¹.     

Basin-scale distributions of stable nitrogen isotopes in the subtropical North Atlantic Ocean: Contribution of diazotroph nitrogen to particulate organic matter and mesozooplankton

New N inputs via biological N₂-fixation play a critical role in supporting oceanic primary production and influencing global biogeochemical cycles. Numerous studies have documented significant N₂-fixation rates in the North Atlantic, but relatively little is known of the pathways and fluxes of new N through planktonic food webs. Here, we report the natural abundance of ¹⁵N in, and contribution of diazotroph N (N_D) inputs to, suspended particles and mesozooplankton collected along two transects in the subtropical North Atlantic Ocean (STNA). Samples were collected in April-May 2000 along the two main transects to evaluate spatial trends of ¹⁵N within the Western Atlantic and across the basin. We found that N₂-fixation is a key component in supporting both primary and secondary productions throughout the STNA. N_D contribution was generally higher for suspended particles than for mesozooplankton, and we observed a high N_D contribution to suspended particles over large spatial scales in the western and central STNA. Mesozooplankton N_D incorporation suggests that diazotroph production supports oceanic food webs over longer timescales (e.g., weeks to months) than that of particle turnover (e.g., days). Larger mesozooplankton (1000-4000 ??m) generally incorporated more N_D than smaller mesozooplankton (250-1000 ??m), and thus may exert a stronger influence on an N_D movement within the water column. Spatial and vertical patterns of variation in mesozooplankton ??¹⁵N also suggest either broad geographical differences in an N_D contribution to secondary production, or temporal variations in N_D incorporation via mesozooplankton communities.     

A new dry combustion method for the simultaneous determination of total organic carbon and nitrogen in seawater

A new dry combustion method for the simultaneous determination of total organic carbon and nitrogen in seawater is presented. Concentrations of total organic carbon obtained using this method average about 2.0 mg/l in surface water and 1.5 mg/l in deep water in the Northwest Atlantic. These concentrations are significantly greater than those reported using wet oxidation and wet combustion methods, but are comparable to concentrations reported by Russian workers using a similar dry combustion method. Organic nitrogen concentrations average 0.44 mg/l in surface water and 0.12 mg/l in deep water, yielding CN ratios for total organic matter of 5 and 12 respectively.     

The alpha/beta ocean distinction: A perspective on freshwater fluxes, convection, nutrients and productivity in high-latitude seas

Stratification is perhaps the most important attribute of oceans with regards to climate and biology. Two simple aspects of the ocean's climate system appear to have a surprisingly important role in transforming waters that feed the global thermohaline circulation, dominating patterns of biogeochemical flux and establishing macroecological domains. First, largely because of meridional distillation (mainly due to the atmospheric transport of freshwater across the Isthmus of Panama) the North Pacific is fresher than the North Atlantic. Second, largely because of zonal distillation (e.g., warming and evaporation at low latitudes and poleward transport of latent heat and moisture by the atmosphere) the upper layers of subtropical seas are permanently stratified by temperature (N_T²=gαdT/dz>0; here called alpha oceans), while the upper layers of high-latitude seas are permanently stratified by salinity (N_S²=gβdS/dz>0; here called beta oceans). The physical basis for the boundary separating alpha and beta oceans is unclear, but may lie in the thermodynamical equations published by Fofonoff [1961. Energy transformations in the sea. Fisheries Research Board of Canada, Report Series 109, 82pp]. Nevertheless, it is clear that the resulting thermohaline distributions establish a ‘downhill journey’ of low-salinity (and nutrient-rich) waters from the North Pacific to the Arctic and then into the North Atlantic. The Arctic Ocean—itself—acts a double estuary, whereby waters entering from the North Atlantic become either denser through cooling (negative estuary) or lighter by freshening (positive estuary) as they circulate within the basin and then return to the North Atlantic as a variety of components of the ocean's conveyor. Intermediate and deep waters generally form within cyclonic beta oceans in close proximity to alphas systems. Similar patterns of stratification, nutrients and biogeographical boundaries persist in the Southern Hemisphere. It is thus argued that this simple distinction—alpha versus beta oceans—provides a broad, conceptual framework for simple interpretation of key physical and biological processes and rates, including the impacts of climate variability.     

A single vs. double spike approach to improve the accuracy of Th measurements in small-volume seawater samples

²³⁴Th is a particle-reactive radionuclide widely used to trace biogeochemical oceanic processes occurring over short timescales. During the last few years, small-volume techniques based on the co-precipitation of ²³⁴Th with MnO₂ coupled with beta-counting have been developed as an alternative to large volume gamma-spectrometric techniques. Here a procedure has been developed to enhance quantitative measurement of ²³⁴Th in MnO₂ precipitates. The main objectives were to obtain a purified Th fraction for beta-counting and to determine the chemical recovery of ²³⁴Th using Th spikes and alpha-spectrometry as an alternative to ICP-MS based methods. Two variations of the procedure are presented. In the first “1 spike” method a ²³⁰Th tracer is added to the sample prior to precipitation of MnO₂, and UTEVA® extraction chromatography is used to obtain a NdF₃(Th) purified source that can be used for both beta-counting of ²³⁴Th and alpha-spectrometry of ²³⁰Th. In the “2 spike” method a ²³⁰Th spike is added and the MnO₂(Th) precipitate is directly beta-counted for ²³⁴Th and subsequently spiked with ²²⁸Th or ²²⁹Th prior to UTEVA® purification and alpha-spectrometry. The results confirm the need to process small-volume seawater samples for ²³⁴Th measurement in presence of a yield tracer, and show that both the 1 spike and 2 spike methods allow an accurate and precise determination of ²³⁴Th (relative percent difference, RPD, between expected and mean measured value < 1%; CV between replicate samples < 3%). Our work also suggests that, although the combined analytical uncertainty on total ²³⁴Th measurements accomplished with both versions of the NdF₃ procedure is promising (6% for 2-L samples), the precision of the ²³⁴Th flux estimation will ultimately depend on the degree of disequilibrium between ²³⁴Th and ²³⁸U.     

基于图相似性匹配的海水溶解氧辅助评价方法

海水溶解氧评价的正确性对于维护海洋生态系统的稳定性具有重要意义。海水溶解氧数据属于非线性时间序列,可视图方法(时间序列转化为图)是分析这类数据较有效的方法,但仍存在未同时考虑数据的时间演变特性以及变量间相互影响的问题。针对现存问题,本研究提出基于图相似性匹配的海水溶解氧辅助评价方法。首先,同时考虑海温、盐度对海水溶解氧的影响以及数据的不可逆性,提出溶氧温盐-转移概率(dissolved oxygen temperature salinity-transition probability, DOTS-TP)有向可视图方法,实现了多变量时间序列到单变量溶解氧图的转化;然后,在将墨西哥湾溶解氧图作为评价参照的基础上,综合利用图的多层次信息,提出子图节点全局(subtree node global, SNG)图相似性匹配方法,通过计算SNG评价指数实现对海水溶解氧的辅助评价。实验结果表明DOTS-TP有向可视图方法能更准确地表达海水溶解氧信息,SNG图相似性匹配方法适用于所有海水溶解氧数据,并能得出正确的辅助评价结果。     

海水中总溶解氮测定的高温燃烧法和湿化学氧化法的比较

对测量海水中总溶解氮(TDN)的两种常用方法——高温燃烧法和过硫酸钾氧化法进行了比较。结果表明,两种方法在空白、精密度和准确度实验中不存在显著差异。对不同化合物的回收率均在92%～107%之间,加标回收实验回归曲线的斜率分别为0.93和0.92。对于现场海水样品的测定结果,两个断面拟合的斜率分别为0.92和0.97。HTC法比PO法对实际海水样品的氧化效率略高,在操作上也更方便、快捷。因此,高温燃烧法更适合海水中总溶解氮(TDN)的测定。     

A preliminary methods comparison for measurement of dissolved organic nitrogen in seawater

Routine determination of dissolved organic nitrogen (DON) is performed in numerous laboratories around the world using one of three families of methods: UV oxidation (UV), persulfate oxidation (PO), or high temperature combustion (HTC). Essentially all routine methods measure total dissolved nitrogen (TDN) and calculate DON by subtracting the dissolved inorganic nitrogen (DIN). While there is currently no strong suggestion that any of these methods is inadequate, there are continuing suspicions of slight inaccuracy by UV methods.This is a report of a broad community methods comparison where 29 sets (7 UV, 13 PO, and 9 HTC) of TDN analyses were performed on five samples with varying TDN and DIN concentrations. Analyses were done in a “blind” procedure with results sent to the first author. With editing out one set of extreme outliers (representing 5 out of 145 ampoules analyzed), the community comparability for analyzing the TDN samples was in the 8–28% range (coefficient of variation representing one standard deviation for the five individual samples by 28 analyses). When DIN concentrations were subtracted uniformly (single DIN value for each sample), the comparability was obviously worse (19–46% cv). This comparison represents a larger and more diverse set of analyses, but the overall comparability is only marginally better than that of the Seattle workshop of a decade ago. Grouping methods, little difference was seen other than inconclusive evidence that the UV methods gave TDN values for several of the samples higher than HTC methods. Since there was much scatter for each of the groups of methods and for all analyses when grouped, it is thought that more uniformity in procedures is probably needed. An important unplanned observation is that variability in DIN analyses (used in determining the final analyte in most UV and PO methods) is essentially as large as the variability in the TDN analyses.This exercise should not be viewed as a qualification exercise for the analysts, but should instead be considered a broad preliminary test of the comparison of the families of methods being used in various laboratories around the world. Based on many independent analyses here, none of the routinely used methods appears to be grossly inaccurate, thus, most routine TDN analyses being reported in the literature are apparently accurate. However, it is not reassuring that the ability of the international community to determine DON in deep oceanic waters continues to be poor. It is suggested that as an outgrowth of this paper, analysts using UV and PO methods experiment and look more carefully at the completeness of DIN conversion to the final analyte and also at the accuracy of their analysis of the final analyte. HTC methods appear to be relatively easy and convenient and have potential for routine adoption. Several of the authors of this paper are currently working together on an interlaboratory comparison on HTC methodology.     

Lipid and 13C signatures of submicron and suspended particulate organic matter in the Eastern Tropical North Pacific: Implications for the contribution of Bacteria

The contribution of bacterial biomass to total particulate organic matter (POM) in the ocean, including exported material, is poorly constrained. To examine potential signatures for the presence and export of bacterioplankton and their detrital remains, here we provide a detailed compound-specific ¹³C characterization of fatty acids from membrane polar lipids obtained from a water column profile in the Eastern Tropical North Pacific. POM of submicron size (0.2–0.7 μm; “X-POM”) was sampled and analyzed separately from the size class typically collected as “suspended” POM (0.7–53 μm; “L-POM”). The distributions of polar head group classes, specific fatty acid side chains, and natural ¹³C contents all vary, both between particle size classes and with depth in the water column. In general, the polar lipids in submicron material – and by inference, lipids of bacterial origin – have higher ¹³C content than polar lipids from larger POM and are equally abundant. Lipid signatures from the photic zone appear to be partially conserved in the suspended pool during transit down the water column. However, bacterial heterotrophy and possibly chemoautotrophy partially overprint these surface signatures. In addition, active metabolisms in the oxygen minimum zone (OMZ) appear to mediate the disaggregation of POM transported from the surface, thus adding complexity to the pathways of mid-water carbon flux and providing additional organic substrates to the OMZ and below. This “substrate injection” may provide important fuel for the denitrification and anammox reactions. Finally, examination of ¹³C content in polar lipids provides a basis for new interpretation of depth-related variations in δ¹³C values of bulk suspended POM.     

适用于快速远程检测海水中氰化物的方法研究

建立了一种适用于海洋远程快速检测氰化物的检测方法,设计了一体化检测装置,未来可搭载到无人艇上实现自动快速检测。针对最佳检测条件进行了一系列优化,得到最佳检测条件:对于100 mL的待测样品,加入酒石酸固体1.5 g;用1～2滴浓度为150 g/L的碳酸钠溶液浸润苦味酸试纸;加热温度80℃,加热时间10min。在最佳检测条件下,检测检出限达0.3mg/L。该方法实现了适用于海水氰化钠的远程检测,大大提高了检测效率,无需人员进入污染现场,安全性高。可广泛用于海洋危化品泄漏、湖泊污染、现场应急筛选等场合的水体样品快速检测。     

Summer phytoplankton blooms in the oligotrophic North Pacific Subtropical Gyre: Historical perspective and recent observations

The export of organic matter from the oceanic euphotic zone is a critical process in the global biogeochemical cycling of bioelements (C, N, P, Si). Much of this export occurs in the form of sinking particles, which rain down into the unlit waters of the deep sea. Classical models of oceanic production and export balance this gravitational loss of particulate bioelements with an upward flux of dissolved nutrients, and they describe reasonably well those areas of the ocean where deep winter mixing occurs. The surface waters of the North Pacific Subtropical Gyre (NPSG), however, are strongly stratified and chronically nutrient-depleted, especially in summer. Nevertheless, there is ample evidence that blooms of phytoplankton and subsequent pulses of particle export occur during the height of summer stratification in these waters, especially to the northeast of the Hawaiian Islands. These blooms impact regional bioelemental cycling and act as a food source to the deep-sea benthos. We review here numerous published observations of these events in the NPSG, and present new data collected at Station ALOHA (22.75°N, 158°W) during the first 176 cruises of the Hawaii Ocean Time-series program (1988-2005), along with results from transect cruises conducted in the region in 1996 and 2005. We suggest that the summer phytoplankton bloom can be considered a frequent, perhaps annual feature in the northeastern NPSG, and that its perceived stochastic nature is a manifestation of chronic undersampling in time and space. The bloom is typically dominated by only a few genera of large diatoms and the cyanobacterium Trichodesmium. It appears to be consistently supported by dinitrogen fixation, but the fate of the organic matter produced during the summer depends critically on the species composition of the responsible diazotrophs. We estimate that the summer bloom is responsible for up to 38% of N₂ fixation and up to 18% of N-based new production annually at Station ALOHA. We hypothesize that the spatial distribution, timing and magnitude of the bloom may be determined largely by the physical and biological processes controlling new phosphorus delivery into the euphotic zone during the summer and the preceding winter.     

A comparison of diatom colonization on natural and artificial substrata in seawater

Experiments to investigate diatom colonization on various substrata in seawater are described. No differences were found due to different methods of preparation of the substrata. Differences in the numbers of diatoms colonizing the different substrata emphasize the care needed in selecting a substratum on which to study the settlement of organisms, especially if the experiments are to be used for subsequent prediction.     

A Comparison of Simulated Particle Fluxes Using NEMURO and Other Ecosystem Models in the Western North Pacific

JGOFS has revealed the importance of marine biological activity to the global carbon cycle. Ecological models are valuable tools for improving our understanding of biogeochemical cycles. Through a series of workshops, the North Pacific Marine Science Organization (PICES) developed NEMURO (North Pacific Ecosystem Model Understanding Regional Oceanography) a model, specifically designed to simulate the lower trophic ecosystem in the North Pacific Ocean. Its ability to simulate vertical fluxes generated by biological activities has not yet been validated. Here compare NEMURO with several other lower trophic level models of the northern North Pacific. The different ecosystem models are each embedded in a common three-dimensional physical model, and the simulated vertical flux of POM and the biomass of phytoplankton are compared. The models compared are: (1) NEMURO, (2) the Kishi and Nakata Model (Kishi et al., 1981), (3) KKYS (Kawamiya et al., 1995, 2000a, 2000b), and (4) the Denman model (Denman and Peña, 2002). With simple NPZD models, it is difficult to describe the production of POM (Particulate Organic Matter) and hence the simulations of vertical flux are poor. However, if the parameters are properly defined, the primary production can be well reproduced, even though none of models we used here includes iron limitation effects. On the whole, NEMURO gave a satisfactory simulation of the vertical flux of POM in the northern North Pacific.     

A high sensitivity method for the determination of nanomolar concentrations of Nitrate and Nitrite in seawater with a technicon autoanalyzer II

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.     

Wet-oxidation and automated colorimetry for simultaneous determination of organic carbon, nitrogen and phosphorus dissolved in seawater

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.