Generation of high resolution sea surface temperature using multi-satellite data for operational oceanography

In the present article, we introduce a high resolution sea surface temperature(SST) product generated daily by Korea Institute of Ocean Science and Technology(KIOST). The SST product is comprised of four sets of data including eight-hour and daily average SST data of 1 km resolution, and is based on the four infrared(IR) satellite SST data acquired by advanced very high resolution radiometer(AVHRR), Moderate Resolution Imaging Spectroradiometer(MODIS), Multifunctional Transport Satellites-2(MTSAT-2) Imager and Meteorological Imager(MI), two microwave radiometer SSTs acquired by Advanced Microwave Scanning Radiometer 2(AMSR2), and Wind SAT with in-situ temperature data. These input satellite and in-situ SST data are merged by using the optimal interpolation(OI) algorithm. The root-mean-square-errors(RMSEs) of satellite and in-situ data are used as a weighting value in the OI algorithm. As a pilot product, four SST data sets were generated daily from January to December 2013. In the comparison between the SSTs measured by moored buoys and the daily mean KIOST SSTs, the estimated RMSE was 0.71°C and the bias value was –0.08°C. The largest RMSE and bias were 0.86 and –0.26°C respectively, observed at a buoy site in the boundary region of warm and cold waters with increased physical variability in the Sea of Japan/East Sea. Other site near the coasts shows a lower RMSE value of 0.60°C than those at the open waters. To investigate the spatial distributions of SST, the Group for High Resolution Sea Surface Temperature(GHRSST) product was used in the comparison of temperature gradients, and it was shown that the KIOST SST product represents well the water mass structures around the Korean Peninsula. The KIOST SST product generated from both satellite and buoy data is expected to make substantial contribution to the Korea Operational Oceanographic System(KOOS) as an input parameter for data assimilation.     

Development of the Operational Oceanographic System of Korea

Ocean Science Journal - The Korea Operational Oceanographic System (KOOS) was developed at the Korea Institute of Ocean Science and Technology (KIOST) to produce real-time forecasting and...     

碘化钾碱性高锰酸钾法测量海水化学需氧量不确定度的研究

葡萄糖与谷氨酸以1:1的比例配制成标准物质,用人工海水和标准物质配制成系列标准溶液,根据碘化钾碱性高锰酸钾法对系列标准溶液的测量结果,获得了海水COD测量不确定度在全量程范围内的分布规律,即测量不确定度在高端大不恒定,在低端小恒定。     

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.     

海水中铯-137的γ能谱测量不确定度评估

为科学评价测量结果的可靠性,对海水中137Cs γ能谱分析方法的不确定度进行了评估。根据《化学分析中不确定度的评估指南》,分析不确定度的来源并逐一对各不确定度分量进行了量化,最终计算了合成相对标准不确定度。结果表明,影响海水中137Cs γ能谱测量不确定度的因素分别为样品源137Cs峰区计数、标准源活度、取样体积、化学回收率、本底137Cs峰区计数及标准源137Cs峰区计数,其中样品源137Cs峰区计数的不确定度贡献最为突出。对于137Cs活度浓度为1.28 mBq/L的海水样品,其合成相对标准不确定度为9.78%。     

碱性高锰酸钾法测量海水化学耗氧量(COD)不确定度的研究

以葡萄糖 谷氨酸为海水COD的标准物质。用人工海水和标准物质配制成系列标准溶液。根据对系列标准溶液的测量结果,获得了碱性高锰酸钾法海水COD测量不确定度的分布规律。     

Permeability measurements in mudrocks using gas-expansion methods on plug and crushed-rock samples

Permeability is an important parameter relative to the production of hydrocarbons in shale oil/gas plays; however, the measurement of permeability in these nano-to microdarcy rocks remains a challenge. Results from different methods or from different laboratories are not consistent, and reasons are not fully understood. In the present study, permeability is measured for both plug and crushed-rock samples with different plug diameter or crushed-sample particle size to systematically investigate the permeability measurement to better understand and apply the measured results. A modified gas-expansion (MGE) method, which can measure permeability for plug samples under confining pressures, was established and applied to several Eagle Ford and Barnett Shale (mudrock) samples. Permeability results from this method are in fair agreement with those from the pulse-decay method. The traditional Gas Research Institute (GRI) method was applied to crushed-rock Eagle Ford Shale samples. The results were comparable to reported permeability for an Eagle Ford Shale sample. Particle or plug size has significant influence on permeability measurement. In general, permeability increases with increasing particle or plug size. For crushed sample with GRI method, the reason of increasing permeability is related to the limitation of the GRI technique and the data analysis method. Estimate of the permeability based on Kozeny–Carman Equation was conducted, and the results were used to evaluate the GRI permeability measurement. Particle size of 2–4 mm (5–10 meshes) is considered as an appropriate size for GRI permeability measurement. For plug sample, larger permeability with larger plug diameter is most likely caused by the artificial fractures. Higher confining pressure can reduce the influence of the fractures, but cannot fully remove it. A range of permeability, defined by the GRI permeability with 2–4 mm particles as the lower boundary and permeability of 1-in plug under high confining pressure (>5000 psi) as the upper boundary, can be a more reliable measures to represent the shale matrix permeability. The range of the permeability also highlights the uncertainty in matrix permeability measurement for shale.     

Automatic colorimetric analyzer prototype for high frequency measurement of nutrients in seawater

This paper describes the characteristics of a prototype of a modular multiparametric analyzer (MicroMAC FAST MP3) for automatic monitoring of seawater and analytical methods for nutrients.The MicroMAC FAST reactor is an evolution of the basic LFA (Loop Flow Analysis) reactor. It has been conceived to assay ammonium, nitrate–nitrite and orthophosphate at low concentration in seawater samples. A sample analysis is 3–4 times faster than that obtainable with a standard LFA reactor. With respect to the previous analyzer a temperature control (30–52 °C) on the measurement cell has been added (only for modules NH₄ and PO₄), while the colorimeter and the related links for transporting the sample have been moved beyond the Loop and form a hydraulic-optical set almost completely independent from the main LFA. All the steps of a wet-chemical colorimetric analysis method are carried out in an analysis cycle sequentially. The hermetic closed Loop provides full protection against background interference, which is a basic requirement for stable trace analysis. At the start of a cycle the loop is washed and filled with sample. The sample color is measured for compensation. Small amounts of concentrated reagents are added and mixed with high intensity. This new technique allows the preparation of two products of reaction which can be introduced at intervals of 150 s in the measurement cell. The intensity of the color of the reaction product is measured on the colorimeter using a monochromatic light beam of specific wavelength. The statistical test shows that the results of automated and manual analyses agree for all the examined parameters. Precision of all three analyses is ≤ 4% RSD.Multiparametric online analyzer: it is possible to connect the analytical modules to a data logger with analogue and digital signals, in order to have online simultaneous analysis of the sample. A typical application is used during research at sea which vessel does not require an operator.     

Reexamination of the fractionation of total dissolved phosphorus in seawater using a modified UV-irradiation procedure,and its application to samples from Suruga Bay and Antarctic Ocean

Application of a modified UV-irradiation procedure to the fractionation of total dissolved phosphorus (TDP) in seawater was examined. By using a peristaltic pump, a sample solution was passed through a quartz column which was coiled around the three Hg-lamps and thus consistently exposed to a controlled UV-irradiation flux. The UV-flux was much lower than that historically employed to hydrolyze total dissolved organic phosphorus (DOP). Before and after the UV-irradiation, colorimetric measurements of soluble reactive phosphorus (SRP) were made by the method of Murphy and Riley (1962) to determine the liberation rate of orthophosphate from P-compounds in the sample. Experiments using 19 different P-compounds indicated that organic phosphate-esters containing only monomers of phosphate were readily decomposed by a 20-minute UV-irradiation period. Release of SRP from organic polyphosphates was minimal. The P released by this procedure is operationally referred to as UV-P. The procedure described herein was employed for fractionation of TDP in seawater. These studies defined several classes of dissolved P: (1) PO₄–P(inorganic phosphate-P), (2) UV-P (Photodecomposable organic-P, most of which consists of organic monophosphate-P), and (3) Org-Poly-P (organic polyphosphate-P). Vertical profiles of DOP and UV-P observed in the oligotrophic regions of Suruga Bay and Antarctic Ocean indicated that UV-P was a major part of total dissolved phosphorus (TDP) in euphotic layers, where inorganic nutrients were probably limiting the active growth of phytoplankton. It is probable that UV-P can be utilized as a source of nutrient-P, in place of PO₄–P.     

Data-based forecasting of beach volumes on monthly to yearly timescales

Data-based methods for forecasting beach volumes are tested using ground-measured bathymetry from Duck, North Carolina, comprising 26 profiles, 20 year duration and one-month resolution. Derived beach volume time series show weak seasonal and strong event signals. The forecasting methods used are: Holt–Winters (standard and modified), three types of linear regression, and a default forecast in which the latest measurement persists unchanged into the future. Improved forecast accuracies are obtained by two modifications to Holt–Winters, involving an autocorrelation correction and long-term trend-damping, and by smoothing the fitting data using running medians or wavelet approximations. Beach volume forecasts are tested mainly at monthly intervals up to 12 months ahead, with further tests at up to 36 months ahead. Overall, modified Holt–Winters performs best and the default forecast second-best. With an added artificial seasonal signal, modified Holt–Winters outperforms the other methods more substantially.     

Coastal environmental assessment and management by ecological simulation in Yeoja Bay, Korea

An eco-hydrodynamic model was used to estimate the carrying capacity of pollutant loads and response of water quality to environmental change in Yeoja Bay, Korea. An energy-system model also was used to simulate the fluctuation in nutrients and organic matter in the bordering wetland. Most water quality factors showed a pulsed pattern, and the concentrations of nutrients and organic matter of seawater increased when input loads of nutrients increased due to freshwater discharge. The well-developed tidal zones and wetlands in the northern area of the bay were highly sensitive to input loads. Residence times of water, chemical oxygen demand (COD), and dissolved inorganic nitrogen (DIN) within the bay were estimated to be about 16 days, 43.2 days, and 50.2 days, respectively. Water quality reacted more sensitively to the effects of nitrogen and phosphorus input than to COD. A plan to reduce the present levels of COD and dissolved inorganic phosphorus (DIP) by 20–30% and DIN by at least 50% in pollutant loads is needed for satisfying the target water quality criteria. The natural removal rate of nutrients in wetlands by reeds was assessed to be approximately 10%.     

Molecular phylogeny of the families Pleuronectidae and Poecilopsettidae (PISCES,Pleuronectiformes) from Korea,with a Proposal for a new classification

A new classification of the Korean pleuronectids was proposed based on a molecular phylogeny using specimens collected from Korea (including some Japanese specimens) between 2008 and 2013. A molecular phylogeny based on partial sequences of the two mitochondrial DNA regions (COI and 16S rRNA) supported the reciprocal monophyly of the three genera, Cleisthenes, Pleuronectes and Pseudopleuronectes. We also found that the genus Poecilopsetta is clearly distinct from Pleuronectidae at the family level. Therefore, the previous classification of the Korean pleuronectids should be changed as follows; two families (Pleuronectidae and Poecilopsettidae), 18 genera, and 26 species. Further research is required to resolve the taxonomic uncertainty of the five species in the genus Limanda, which clustered into two clades in our analysis.     

东海近海水质活性磷测定的不确定度探讨

采用国际通用的方法研究了东海近海水质活性磷测定中的不确定度,分析了现场特定环境、测量标准、取样体积、摩尔质量等因素对测量不确定度的影响,评估了各参数的标准不确定度、合成标准不确定度和扩展不确定度.结果表明,现场特定环境是影响东海近海水质活性磷测定中不确定度的主要因素;东海近海水质活性磷测定中的相对合成标准不确定度约为0.067.     

Doubling the production and precision of the MBTH spectrophotometric assay for dissolved carbohydrates in seawater

Extensive use of the three step 3-methyl-2-benzothiazolinone hydrazone hydrochloride (MBTH) method for determining concentrations of both free and combined dissolved carbohydrate occurring in diverse marine environments has shown its suitability for studies of carbohydrate dynamics. Modification of the analytical sequence to extend over 2 working days to eliminate a confusing and error producing overlap of analytical operations allows a single analyst to determine 15 instead of 8 samples in the same 2-day period. This modification also permits an increase in the number of blank plus replicate determinations from 5 to 7 per sample so that a total of 105 reaction tubes can be assayed every 2 days compared to 40–50 for the original procedure. For a series of 7 Narragansett Bay samples, the standard deviation of the method serendipitously decreased by 50% (from ±5.3 to ±2.7 μg C l⁻¹) when the original procedure was compared with the modified procedure. Postponing the final analytical step for a day when the analyses can be completed with an autoprocessor will free the analyst for the processing of more samples, causing an additional doubling in productivity.     

东海近海水质无机氮类测定中的不确定度探讨

分析探讨了东海近海水质无机氮类测定中不确定度的影响因素。其中,考虑到海洋环境监测的一些特殊性,在建立评定不确定度分量的数学模型时,引入了重复性实验校正因子f,并选取2004年东海区海洋环境监测中不同海域的试样进行原始平行性测定资料,以A类方式评定量化重复性实验校正因子f的不确定度分量;同时,以A类或B类的方式对近海水质无机氮类测定中的其它各个不确定度分量进行了评定。结果表明,NH_4~ 测定的相对合成标准不确定度分量最大,重复性实验校正因子f是近海水质无机氮类测定不确定度的主要来源。在此基础上,计算了东海近海水质无机氮类(NO_2~-、NO_3~-、NH_4~ )测定中的相对合成标准不确定度分别约为0.080,0.034,0.10。     

Optimisation of a catalytic procedure for the determination of total iodine in seawater

A precise method for the determination of total iodine in seawater, which uses a Technicon Auto-Analyser II system and is based on Truesdale and Spencer's (1974) and Truesdale and Smith's (1975) earlier works with a catalytic procedure, is described. The procedure operates over a range of 30–80 μg1^?1 of iodine. As requested by Mark (1973), the way in which the procedure can be varied to suit other applications, and therefore ranges, is explained in detail. The standard deviation at the 50 μg1^?1 level was found to be 0.12 μ1^?1 showing that the method's precision exceeds most, if not all, previously published procedures for this variable. This high degree of resolution makes the procedure suitable for oceanic investigations. The effects of varying the reaction time, the temperature at which the reaction proceeds and the salinity of samples and standards are described. The advantages of using a Technicon Auto-Analyser II system rather than an Auto-Analyser I system are discussed. With slight modification the procedure can also be used in the measurement of river flow where sodium iodide is used as tracer in the dilution method.     

Comparison of anchovy biomass estimates measured by trawls,egg production methods and hydro-acoustics in the Chesapeake Bay and the Korea Strait

We compared estimates of anchovy biomass derived from trawl surveys, egg production method (EPM) and acoustic surveys, conducted in two remote regions. Biomass density of bay anchovy Anchoa mitchilli was estimated in Chesapeake Bay, USA, by trawls, EPM and acoustics from 1989 to 2000. Biomass density of Pacific anchovy Engraulis japonicus was estimated in the Korea Strait using EPM, simulation-based daily cohort analysis and acoustics from 1984 to 2006. Most of the existing estimates already had considered body-size-dependent gear selectivity, highlyvariable instantaneous natural mortality of anchovy eggs, and avoidance of trawl nets by adult anchovy. Despite great variability in the ratio of trawl to acoustic biomass estimates (0.034–8.35), annually-averaged biomass density of young-ofthe-year individuals derived by the two methods were similar for bay anchovy in Chesapeake Bay and Pacific anchovy in the Korea Strait (0.83 and 0.70 g m^?3, respectively). Results suggested that, despite substantial uncertainty, anchovy biomass estimates are generally compatible between EPM and acoustics. However, reported estimates of biomass density derived from the two acoustic surveys in the Korea Strait differed by a factor of 28, suggesting that further improvements in calibrations are required to reliably estimate anchovy biomass. The comparisons suggested that all biomass estimates could be biased and will require comparison and validation by other, independent sampling methods.     

碱性高锰酸钾法海水化学耗氧量(COD)在线测量仪的研制

一种新型的海水COD在线测量仪已经研制出来,其采用了碱性高锰酸钾法和流动注射分析技术,仪器的测量结果与标准方法有很好的一致性,它们的相关系数超过0.98。     

Th isotopes in the Santa Monica basin: Temporal variation,long-term mass balance and model rate constants

Distribution and flux of²³⁴Th,²³²Th and²³⁰Th in the water column of central Santa Monica basin observed over a period of seven years show seasonal and interannual variabilities. A steady-state model is applied to the integrated data to calculate long term average flux and model rate constants of Th isotopes. Mass balance calculations show that the basin acts like a closed system for short-lived²³⁴Th, but not for the long-lived isotopes²³⁰Th and²³²Th. Most²³⁰Th in the basin is transported from elsewhere. Of the incoming Th, 40–55% of the²³⁰Th and 14–26% of the²³²Th enter the surface water in dissolved form. In the upper 100 m, the residence time of dissolved Th with respect to adsorption onto suspended particulates, 70–80 days, is about one order of magnitude higher than the residence time of suspended particles with respect to aggregation into sinking particles, 7–10 days.     

A simple indirect method for the determination of organic-carbon in marine particles

A simple indirect method for the determination of organic carbon in marine particulate matter is proposed. The recommended procedure is as follows: The dried sample is ashed at 450°C for about 24 hr. The ashed sample is put into a Teflon vessel followed by a mixed solution of nitric acid, perchloric acid and hydrofluoric acid. The vessel is sealed and allowed to stand at 150°C for 5 hr. The concentrations of Si and Al in the digested solution are determined. The organic carbon content (Cal-C, %) is calculated by the following equation: Cal-C=0.52 ([CF]–0.10 [Opal]–0.03 [A-Si]), where [CF] is the combustible fraction (%), [Opal] is the biogenic-SiO₂(%), and [A-Si] is the content of aluminosilicate mineral (%).