Release of dissolved organic matter during oxic and anoxic decomposition of salt marsh cordgrass

Chromophoric dissolved organic matter (CDOM), as the light absorbing fraction of bulk dissolved organic matter (DOM), plays a number of important roles in the global and local biogeochemical cycling of dissolved organic carbon (DOC) and in controlling the optical properties of estuarine and coastal waters. Intertidal areas such as salt marshes can contribute significant amounts of the CDOM that is exported to the ocean, but the processes controlling this CDOM source are not well understood. In this study, we investigate the production of DOM and CDOM from the decomposition of two salt marsh cordgrasses, Spartina patens, a C₄ grass, and Typha latifolia, a C₃ grass, in well-controlled laboratory experiments. During the seven-week incubation period of the salt marsh grasses in oxic and anoxic seawater, changes in dissolved organic carbon (DOC) concentrations, dissolved nitrogen (DN) concentrations, stable carbon isotopic composition of DOC (DOC-δ¹³C), and CDOM fluorescence demonstrate a significant contribution of DOC and CDOM to estuarine waters from salt marsh plants, such as Spartina and Typha species. In the natural environment, however, the release processes of CDOM from different cordgrass species could be controlled largely by the in situ oxic and anoxic conditions present during degradation which affects both the production and decomposition of DOC and CDOM, as well as the optical properties of CDOM in estuarine and coastal waters.     

Spatial and Temporal Distribution of Coloured Dissolved Organic Matter (CDOM) in Narragansett Bay,Rhode Island: Implications for Phytoplankton in Coastal Waters

One indicator of health in estuarine and coastal ecosystems is the ability of local waters to transmit sunlight to planktonic, macrophytic, and other submerged vegetation for photosynthesis. The concentration of coloured dissolved organic matter (CDOM) is a primary factor affecting the absorption of incident sunlight in coastal and estuarine waters. In estuaries, CDOM concentrations vary due to changes in salinity gradients, inflows of industrial and domestic effluents, and the production of new dissolved organic matter from marine biologic activity. CDOM absorption data have been collected from a variety of waters. However, there are a limited number of measurements along the US east coast and a general lack of data from New England waters.This study characterized the temporal and spatial variability of CDOM absorption over an annual cycle in Narragansett Bay and Block Island Sound (Rhode Island). Results suggested that, in Narragansett Bay, the magnitude of CDOM absorption is related to the seasonal variability of freshwater input from surrounding watersheds and new CDOM production from in situ biologic activity. The data show that the average CDOM absorption coefficient at 412 nm was 0·45 m⁻¹ and the average spectral slope was 0·020 nm⁻¹.     

High-resolution measurements of chromophoric dissolved organic matter in the Mississippi and Atchafalaya River plume regions

Chromophoric dissolved organic matter (CDOM) was measured in the spring and summer in the northern Gulf of Mexico with the ECOShuttle, a towed, instrumented, undulating vehicle. A submersible pump mounted on the vehicle supplied continuously flowing, uncontaminated seawater to online instruments in the shipboard laboratory and allowed discrete samples to be taken for further analysis. CDOM in the northern Gulf of Mexico was dominated by freshwater inputs from the Mississippi River through the Birdfoot region and to the west by discharge from the Atchafalaya River. CDOM was more extensively dispersed in the high-flow period in the spring but in both time periods was limited by stratification to the upper 12 m or so. Thin, subsurface CDOM maxima were observed below the plume during the highly stratified summer period but were absent in the spring. However, there was evidence of significant in situ biological production of CDOM in both seasons.The Mississippi River freshwater end member was similar in spring and summer, while the Atchafalaya end member was significantly higher in the spring. In both time periods, the Atchafalaya was significantly higher in CDOM and dissolved organic carbon (DOC) than the Mississippi presumably due to local production and exchange within the coastal wetlands along the lower Atchafalaya which are absent along the lower Mississippi. Nearshore waters may also have higher CDOM due to outwelling from coastal wetlands. High-resolution measurements allow the differentiation of various water masses and are indicative of rapidly varying (days to weeks) source waters. Highly dynamic but conservative mixing between various freshwater and marine end members apparently dominates CDOM distributions in the area with significant in situ biological inputs (bacterial degradation of phytoplankton detritus), evidence of flocculation, and minor photobleaching effects also observed. It is clear that high-resolution measurements and adaptive sampling strategies allow a more detailed examination of the processes that control CDOM distributions in river-dominated systems.     

Correlation of the absorption coefficient with a reduction in mean mass for dissolved organic matter in southwest Florida river plumes

Results are presented from an investigation of the relationship between molecular mass distribution and optical properties for colored dissolved organic matter (CDOM); a complex assembly of organic macromolecules of marine and freshwater origin found throughout the surface ocean. Unique data are derived from the application of a new technique, a combination of a hydrophilic–lipophilic copolymer-based solid phase extraction (SPE) with electrospray ionization (ESI) continuous flowing ion trap mass spectrometry (cf-MS), for the direct determination of CDOM mass distribution. An evaluation of this copolymer-based extraction technique for the analysis of Suwannee River Natural Organic Matter (SRNOM) reference material revealed that the current method compares favorably with C₁₈ modified silica or XAD resin-based extraction methods reported in the literature when considering extraction efficiency or low extraction bias for CDOM. The mass distribution of CDOM in several freshwater to marine transition zones along coastal southwestern Florida has been determined with this technique. All rivers in the study region had a bimodal distribution of masses. A case study of the Caloosahatchee River outflow CDOM mass distribution data are presented as an example of the modification in mass distributions. The lower mass mode of the bimodal distribution was observed to have a relatively stable mean throughout the study region at 406±9 Da, while decreasing in concentration in a non-conservative manner with salinity. In contrast, the upper mass mode of the bimodal distribution was observed to have a variable mean, reaching 1408 Da in the least saline waters and decreasing by 174 Da through the transect toward higher salinity coastal waters. Coinciding with this reduction in mean mass for the upper distribution is a non-conservative reduction in concentration when compared with salinity. We define apparent organic carbon (AOC) as a function of the cf-MS determined total integrated area and use this value to determine concentration of the total extracted CDOM. Unique correlations between the CDOM fluorescence (350-nm excitation/450-nm emission) and the AOC for these coastal samples have been observed for each of three rivers in the study region. The steepest slope and highest correlation between optical and mass spectral properties are observed in rivers with strongly absorbing waters originating in the Florida Everglades and lowest in rivers draining clearer waters from widely variable and anthropogenic influenced regions. The trends in molecular mass distribution and corresponding optical properties support the theory that CDOM in coastal zones is environmentally processed material from terrestrial sources. Probable cause of the reduction in mean mass and suggestions for further investigation of sources and transformations of CDOM are discussed.     

大洋河河口海域有色溶解性有机物的光学特性及遥感反演模型

有色溶解性有机物(CDOM)在河口混合过程中近似呈保守行为,可作为水团运动的示踪剂.基于2009年5月6日大洋河河口海域水体调查的实测数据,对该区域CDOM光学特性及遥感反演模型进行了研究,结果表明:研究区域CDOM主要来自河流输入,成分相对较稳定,属于典型的近岸二类水体区域;波长275～295 nm的光谱斜率和波长4...     

An optical model for the remote sensing of coloured dissolved organic matter in coastal/ocean waters

An optical model is developed for the remote sensing of coloured dissolved organic matter (CDOM) in a wide range of waters within coastal and open ocean environments. The absorption of CDOM (denoted as a_g) is generally considered as an exponential form model, which has two important parameters – the slope S and absorption of CDOM at a reference wavelength a_g(λ₀). The empirical relationships for deriving these two parameters are established using in-situ bio-optical datasets. These relationships use the spectral remote sensing reflectance (R_rs) ratio at two wavelengths R_rs(670)/R_rs(490), which avoids the known atmospheric correction problems and is sensitive to CDOM absorption and chlorophyll in coastal/ocean waters. This ratio has tight relationships with a_g(412) and a_g(443) yielding correlation coefficients between 0.77 and 0.78. The new model, with the above parameterization applied to independent datasets (NOMAD SeaWiFS match-ups and Carder datasets), shows good retrievals of the a_g(λ) with regression slopes close to unity, little bias and low mean relative and root mean square errors. These statistical estimates improve significantly over other inversion models (e.g., Linear Matrix-LM and Garver-Siegel-Maritorena-GSM semi-analytical models) when applied to the same datasets. These results demonstrate a good performance of the proposed model in both coastal and open ocean waters, which has the potential to improve our knowledge of the biogeochemical cycles and processes in these domains.     

Coloured dissolved organic matter (CDOM) in Southern North Sea waters: Optical characterization and possible origin

The variability and origin of the Coloured Dissolved Organic Matter (CDOM) were studied in the Belgian coastal and adjacent areas including offshore waters and the Scheldt estuary, through the parameters: absorption at 375 nm, a_CDOM(375), and the slope of the absorption curve, S. a_CDOM(375) varied between 0.20 and 1.31 m⁻¹ and between 0.97 and 4.30 m⁻¹ in the marine area and Scheldt estuary, respectively. S fluctuated between 0.0101 and 0.0203 nm⁻¹ in the marine area and between 0.0167 and 0.0191 nm⁻¹ in the Scheldt estuary. The comparative analysis of a_CDOM(375) and S variations evidenced different origins of CDOM in the BCZ. The Scheldt estuarine waters showed decreasing a_CDOM(375) values with increasing salinity but constant S value of ∼0.018 nm⁻¹ suggesting a dominant terrestrial origin of CDOM. On the contrary, samples collected in the marine domain showed a narrow range of a_CDOM(375) but highly variable S suggesting the additional presence of autochthonous sources of CDOM. This source was evidenced based on the sorting of the marine offshore data according to the stage of the phytoplankton bloom when they were collected. A clear distinction was made between CDOM released during the growth stage characterized by high S (∼0.017 nm⁻¹) and low a_CDOM(375) and the decay phase characterized by low S (∼0.013 nm⁻¹) and high a_CDOM(375). This observation was supported by CDOM measurements performed on pure phytoplankton cultures which showed increased CDOM release along the wax and wane of the bloom but decreasing S. We concluded that the high variability of the CDOM signature in offshore waters is explained by the local biological production and processing of CDOM.     

Spatial and temporal distribution of chromophoric dissolved organic matter (CDOM) fluorescence and its contribution to light attenuation in UK waterbodies

Vertical attenuation of light through the water column (K_d) is attributable to the optically active components of phytoplankton, suspended particulate material (SPM) and chromophoric dissolved organic matter (CDOM). Of these, CDOM is not routinely monitored and was the main focus of this study. Concentrations and spatio-temporal patterns of CDOM fluorescence were investigated between August 2004 and March 2006, to quantify the correlation coefficient between CDOM and salinity and to better characterise the contribution of CDOM to K_d. Sampling was conducted at a broad range of UK and Republic of Ireland locations; these included more than 15 estuaries, 30 coastal and 70 offshore sites in the southern North Sea, Irish Sea, Liverpool Bay, Western Approaches and the English Channel.An instrument package was used; a logger with multi-sensor array was deployed vertically through the water column and concurrent water samples were taken to determine salinity, CDOM fluorescence and SPM. Surface CDOM fluorescence values ranged between 0.05 and 16.80 S.Fl.U. (standardised fluorescence units). A strong, negative correlation coefficient of CDOM to salinity (r² = 0.81) was found. CDOM absorption (aCDOM_λ) was derived from fluorescence measurements and was in the range 0.02–2.2 m⁻¹ with mean 0.15 m⁻¹. These results were comparable with direct measurements of aCDOM_λ in the same geographic regions, as published by other workers.Spatial differences in CDOM fluorescence were generally explicable by variation in salinity, in local conditions or catchment areas; e.g. CDOM at the freshwater end was 3.54–11.30 S.Fl.U., reflecting the variety of rivers sampled and their different catchments. Temporal changes in CDOM fluorescence were related to salinity. A significant and positive correlation was found between CDOM and K_d, and although CDOM was found to be less influential than SPM on K_d, it was still of significance particularly in coastal and offshore waters of lower turbidity.     

Photobleaching of chromophoric dissolved organic matter in natural waters: kinetics and modeling

The effects of monochromatic and polychromatic UV and visible (VIS) radiation on the optical properties (absorption and fluorescence) of chromophoric dissolved organic matter (CDOM) were examined for a Suwannee River fulvic acid (SRFA) standard and for water from the Delaware and Chesapeake Bays. The primary (direct) loss of absorption and fluorescence occurred at the irradiation wavelength(s), with smaller secondary (indirect) losses occurring outside the irradiation wavelength(s). The efficiency of both direct and indirect photobleaching decreased monotonically with increasing wavelength. Exposure to polychromatic light increased the CDOM absorption spectral slope (S), consistent with previous field measurements. An analysis of the monochromatic photobleaching kinetics argues that a model based on a simple superposition of multiple chromophores undergoing independent photobleaching cannot apply; this conclusion further implies that the absorption spectrum of CDOM cannot arise solely from a simple superposition of the spectra of numerous independent chromophores. The kinetics of CDOM absorption loss with the monochromatic irradiation were employed to create a simple, heuristic model of photobleaching. This model allowed us to examine the importance of the indirect photobleaching losses in determining the overall photobleaching rates as well as to model the photobleaching of natural waters under polychromatic light fields. Application of this model to natural waters closely predicted the change in the CDOM spectral shape caused by photodegradation. The time scale of this process was consistent with field observations acquired during the summertime for coastal waters in the Middle Atlantic Bight (MAB). The results indicate that the ratio of the photodegradation depth to the mixed layer depth is a key parameter controlling the rate of the photobleaching in surface waters.     

Behaviour of the optical properties of coloured dissolved organic matter under conservative mixing

The optical properties of coloured dissolved organic matter (CDOM) can be used, in some environments, to trace water masses and provide information about the dynamics of the dissolved organic fraction in natural waters. This work presents the results from a modelling exercise, laboratory experiment and field data, which describe the variations in the optical properties of CDOM during mixing. The exponential slope coefficient (S) is frequently used to characterise different CDOM pools; however, its behaviour during conservative mixing of two different CDOM types is often misunderstood. Identification of a theoretical conservative mixing line allows the rapid identification of non-conservative processes (e.g. in situ production, flocculation and degradation) acting on the pool during mixing. The results suggest that some of the patterns reported in the literature could purely be a result of conservative mixing rather than a product of non-conservative processes.     

Seasonal and spatial variations in the partial pressure of carbon dioxide in a eutrophic brackish lake,Lake Hamana,Japan

The dissolved inorganic carbon and total alkalinity in the surface brackish waters of Lake Hamana were investigated monthly from October 2017 to September 2019 at 14 stations. The partial pressure of carbon dioxide (pCO₂) in the surface water ranged from 29 to 1476 μatm and was undersaturated for atmospheric CO₂ during the observation periods, although most coastal waters were net source areas because of the large amount of terrestrial organic and inorganic carbon input. Since there was a strong negative correlation between pCO₂ and the dissolved oxygen, seasonal and temporal variations in pCO₂ were mainly derived from phytoplankton activity. The high phytoplankton activity induced by the effluents from sewage treatment plants, which was low in carbon and high in nitrogen. Therefore, in urbanized coastal waters with sewage treatment plants, such as the coastal waters of Japan, there is a possibility of shifting from weaker carbon dioxide source areas to sink areas. However, pCO₂ was oversaturated at the polluted river mouth, especially after high precipitation events due to the large carbon supply.

     

Seasonal dynamics of light absorption by chromophoric dissolved organic matter (CDOM) in the NW Mediterranean Sea (BOUSSOLE site)

We analyze a two-year time-series of chromophoric dissolved organic matter (CDOM) light absorption measurements in the upper 400 m of the water column at the BOUSSOLE site in the NW Mediterranean Sea. The seasonal dynamics of the CDOM light absorption coefficients at 440 nm (a_cdom(440)) is essentially characterized by (i) subsurface maxima forming in spring and progressively reinforcing throughout summer, (ii) impoverishment in the surface layer throughout summer and (iii) vertical homogeneity in winter. Seasonal variations of the spectral dependence of CDOM absorption, as described by the exponential slope value (S_cdom), are characterized by highest values in summer and autumn at the surface and low values at the depths of a_cdom(440) subsurface maxima or just below them. Variations of a_cdom(440) are likely controlled by microbial digestion of phytoplankton cells, which leads to CDOM production, and by photochemical destruction (photobleaching), which leads to CDOM degradation. Photobleaching is also the main driver of S_cdom variations. Consistently with previous observations, a_cdom(440) for a given chlorophyll a concentration is higher than expected from Case I waters bio-optical models. The total non-water light absorption budget shows that surface waters at the BOUSSOLE site are largely dominated by CDOM during all seasons but the algal bloom in March and April. These results improve the knowledge of CDOM absorption dynamics in the Mediterranean Sea, which is scarcely documented. In addition, they open the way to improved algorithms for the retrieval of CDOM absorption from field or satellite radiometric measurements.     

基于遥感反演的浒苔绿潮暴发对有色溶解有机物与叶绿素时空分布特征的影响

浒苔的暴发会对水体生态环境产生巨大的影响, 对此进行遥感监测具有十分重要的意义。本文基于现场同步实测的有色溶解有机物(colored dissolved organic matter, CDOM)吸收系数、叶绿素浓度以及光谱数据建立遥感反演模型,再结合MODIS卫星影像提取山东半岛南侧近岸海域在各年份浒苔暴发前后CDOM与叶绿素浓度的时空分布特征。结果表明, 浒苔的消亡分解会在水体中产生大量的CDOM, 但浒苔的生长繁殖同样会消耗CDOM, 此外CDOM还受到浒苔暴发时期强烈的光降解作用。在各种因素的综合作用下, 研究区海域CDOM浓度在浒苔暴发时期微弱升高, 浒苔消亡后CDOM浓度则开始回落。浒苔在暴发期会抑制其他浮游微藻的生长, 使研究区海域叶绿素浓度有所降低, 而浒苔消亡后叶绿素浓度有所上升。水体中的叶绿素受多种生物地球化学因素的影响, 因此叶绿素浓度的降低与浒苔的暴发强度之间没有明确的相关性。遥感反演可以大范围快速地提取水体中各种要素的分布情况, 但就浒苔的暴发对海水中各要素的影响机制而言, 还需要结合各种生态环境因子进行综合分析。     

Chromophoric dissolved organic matter and dissolved organic carbon in Chesapeake Bay

Chromophoric dissolved organic matter (CDOM) is the light absorbing fraction of dissolved organic carbon (DOC). The optical properties of CDOM potentially permit remote sensing of DOC and CDOM, and correction for CDOM absorption is essential for remote sensing of chlorophyll a (chl a) in coastal and estuarine waters. To provide data for this purpose, we report the distributions of CDOM, DOC, and chl a from seven cruises in Chesapeake Bay in 1994–1997. We observed non-conservative distributions of chl a and DOC in half of the cruises, indicating net accumulations within the estuary; however, there were no net accumulations or losses of CDOM, measured as absorption at 355 nm or as fluorescence. Freshwater end member CDOM absorption varied from 2.2 to 4.1 m⁻¹. Coastal end member CDOM absorption was considerably lower, ranging over 0.4–1.1 m⁻¹. The fluorescence/absorption ratio was similar to those reported elsewhere for estuarine and coastal waters; however, in the lower salinity/high CDOM region of the Bay, the relationship was not constant, suggestive of the mixing of two or more CDOM sources. Chl a was not correlated with the absorption for most of the cruises nor for the data set as a whole; however, CDOM and DOC were significantly correlated, with two groups evident in the data. The first group had high CDOM concentrations per unit DOC and corresponded to the conservative DOC values observed in the transects. The second group had lower CDOM concentrations per unit DOC and corresponded to the non-conservative DOC values associated with net DOC accumulation near the chl a maximum on the salinity gradient. This indicates the production of non-chromophoric DOC in the region of the chl a maximum of Chesapeake Bay. In terms of remote sensing, these data show that (1) the retrieval of the absorption coefficient of CDOM from fluorescence measurements in the Bay must consider the variability of the fluorescence/absorption relationship, and (2) estimates of DOC acquired from CDOM absorption will underestimate DOC in regions with recent, net accumulations of DOC.     

CDOM and its contribution to the underwater light climate of a shallow, microtidal estuary in south-western Australia

Light attenuation (K_d) of photosynthetically active radiation (PAR) by chromophoric dissolved organic matter (CDOM), total suspended solids (TSS) and chlorophyll a (Chl a) were measured at nine stations along an estuarine gradient in the Swan River, Western Australia, over 15 months. There were strong spatial gradients associated with the marine-freshwater transition along the 32 km of estuary sampled, as well as seasonal gradients mainly associated with rainfall, 80% of which occurs between May and September. CDOM absorbances at 440 nm reached a maximum of 10.9 m⁻¹ with the freshwater inflow but concentrations of suspended matter remained low throughout the sampling period (1.0–21.0 mg l⁻¹) under the diurnal tides of the estuary. CDOM was the dominant constituent of K_d and a stepwise multiple regression showed that 66% (p < 0.0001) of the variation in K_d can be explained by CDOM and an additional 8% (p < 0.0001) by TSS. As a consequence of this result, analysis into the influence of river discharge rates on CDOM absorbance levels was examined for 2002 using data collected during this study, and for 2000 and 2001 using historical dissolved organic carbon (DOC) and river discharge data. The outcome of this analysis infers that greater river discharge rates result in increased CDOM absorbances in the Swan River estuary.     

珠江口溶解有机物的遥感动态监测

河口有色溶解有机物（colored dissolved organic matter,CDOM）的分布是各种物理-生物地球化学过程共同作用的结果。为实现河口高动态变化CDOM的监测,遥感是一种重要的手段。由珠江口四个不同季节的航次获得的实测数据,本文构建了一个遥感算法以反演CDOM在400 nm的吸收系数（a_CDOM （400））。该算法使用以波段反射率比值R_rs （667）/R_rs （443）和R_rs （748）/R_rs （412）为自变量。将构建的算法应用于2002-2014年的MODIS/Aqua数据,本文计算了珠江口不同季节的a_CDOM （400）气候态分布。CDOM的分布主要受珠江径流量和区域水下地形特征的影响。沿着垂直于水深梯度的断面,气候态a_CDOM （400）呈指数减少（y=ae^bx,b<0）,但不同季节差异很大。珠江口CDOM主要是河流淡水输运而来。其中,富里酸比例随盐度的增加而降低。基于构建的算法、CDOM保守混合方程和径流量,本文由MODIS/Aqua数据进一步估算了2002-2014年夏季和冬季珠江DOC的有效入海浓度和有效入海通量。珠江的有效入海浓度和有效入海通量都与流量存在正相关关系,且在夏季的相关性更明显,R2分别为0.698和0.9657。     

Characterization of dissolved organic matter fluorescence in the South Atlantic Bight with use of PARAFAC model: Interannual variability

Systematic water sampling for characterization of chromophoric dissolved organic matter (CDOM) in the coastal South Atlantic Bight, was conducted as part of the long term Coastal Ocean Research and Monitoring Program (CORMP). Water samples were collected during a 3.5 year period, from October 2001 until March 2005, in the vicinity of the Cape Fear River (CFR) outlet and in adjacent Onslow Bay (OB). During this study there were two divergent hydrological and meteorological conditions in the CFR drainage area: a severe drought in 2002, followed by the very wet year of 2003. CDOM was characterized optically by the absorption coefficient at 350 nm, the spectral slope coefficient (S), and by Excitation Emission Matrix (EEM) fluorescence. Parallel Factor Analysis (PARAFAC) was used to assess CDOM composition from EEM spectra and six components were identified: three terrestrial humic-like components, one marine humic-like component and two protein-like components. Terrestrial humic-like components contributed most to dissolved organic matter (DOM) fluorescence in the low salinity plume of the CFR. The contribution of terrestrial humic-like components to DOM fluorescence in OB was much smaller than in the CFR plume area. Protein-like components contributed significantly to DOM fluorescence in the coastal ocean of OB and they dominated DOM fluorescence in the Gulf Stream waters. Hydrological conditions during the observation period significantly impacted both concentration and composition of CDOM found in the estuary and coastal ocean. In the CFR plume, there was an order of magnitude difference in CDOM absorption and fluorescence intensity between samples collected during the drought compared to the wet period. During the drought, CDOM in the CFR plume was composed of equal proportions of terrestrial humic-like components (ca. 60% of the total fluorescence intensity) with a significant contribution of proteinaceous substances (ca. 20% of the total fluorescence). During high river flow, CDOM was composed mostly of humic substances (nearly 75% of total fluorescence) with minor contributions by proteinaceous substances. The impact of changes in fresh water discharge patterns on CDOM concentration and composition was also observed in OB, though to a lesser degree.     

The variations in optical properties of CDOM throughout an algal bloom event

For studies in bio-optical oceanography, visible light properties by classes of dissolved organic matter should be characterized. The regional adjustment of model parameters is one approach which is being widely used to refine bio-optical models. In the present study, buoy and laboratory data were acquired, and during the 15-day observation period an algal bloom event occurred. The absorption coefficient of CDOM at 443 nm, a_g(443), changed in the range of 0.09–0.35 m⁻¹ and 0.1–0.34 m⁻¹ for two depths, 0.32 m and 2.3 m., respectively, throughout the entire period. CDOM absorption was larger for bloom conditions than for non-bloom conditions. In addition, the fraction of CDOM in total absorption was higher during the bloom event than that of non-bloom conditions. The spectral slope of CDOM absorption, S_g, regressed over 400–500 nm, ranged from 0.015 to 0.0185 nm⁻¹ with an average of 0.0166 nm⁻¹. CDOM fluorescence intensity (Fcdom) was obtained using an internal Raman standard and varied over the range of 467.44–1538.23 in relative units. Variations in Fcdom showed a similar pattern to that of CDOM absorption. A robust non-linear relationship between Fcdom and CDOM absorption was found, with a correlation coefficient of 0.893, throughout the whole observation. An attempt to describe S_g with absorption showed a promising consequence that can be described with a negative correlation during the bloom, however, without any distinguishable tendency for non-bloom time span. A two-band ratio algorithm was also carried out for retrieving CDOM absorption. The variations in optical properties of CDOM may be related to the complicated environment in the estuarine waters, which may result from different sources of CDOM.     

南海北部上层鱼类浮游生物多样性和丰度的季节变化

The objective of this study was to investigate the seasonal variations of ichthyoplankton diversity and abun-dance in the northern South China Sea based on the data collected during summer, winter and spring. In total, 95 taxa of larval fishes were identified. The greatest number of species was recorded in spring, followed by summer and winter. The number of species was distributed mainly in the coastal waters from the east of Leizhou Peninsula to the southeast of Hainan Island during the surveyed periods of summer and spring, but in the offshore waters during winter. The abundance of larval fish was lowest in winter, increased in spring, and reached the maximum in summer. High abundance of larval fish was generally restricted to coastal waters with the isobaths less than 50 m. Seasonal variations of larval fish richness, abundance and diversity index were significant （P〈0.001）. Carangidae was the most common and abundant taxon in summer and winter, whileSardinella sp.,Thrissa mystax andLeiognathus sp. were dominant in spring. High diversity and abundance of larval fish might be attributed to increased temperature and coastal upwelling in spring and summer.     

Initial validation of GOCI water products against in situ data collected around Korean peninsula for 2010–2011

This paper provides initial validation results for GOCI-derived water products using match-ups between the satellite and ship-borne in situ data for the period of 2010?C2011, with a focus on remote-sensing reflectance (R _rs ). Match-up data were constructed through systematic quality control of both in situ and GOCI data, and a manual inspection of associated GOCI images to identify pixels contaminated by cloud, land and inter-slot radiometric discrepancy. Efforts were made to process and quality check the in situ R _rs data. This selection process yielded 32 optimal match-ups for the R _rs spectra, chlorophyll a concentration (Chl_a) and colored dissolved organic matter (CDOM), and with 20 match-ups for suspended particulate matter concentration (SPM). Most of the match-ups are located close to shore and thus the validation should be interpreted limiting to near-shore coastal waters. The R _rs match-ups showed the mean relative errors of 18?C33% for the visible bands with the lowest 18?C19% for the 490 nm and 555 nm bands and 33% for the 412 nm band. Correlation for the R _rs match-ups was high in the 490?C865 nm bands (R²=0.72?C0.84) and lower in the 412 nm band (R²=0.43) and 443 nm band (R²=0.66). The match-ups for Chl_a showed a low correlation (<0.41) although the mean absolute percentage error was 35% for the GOCI standard Chl_a. The CDOM match-ups showed an even worse comparison with R²<0.2. These match-up comparison for Chl_a and CDOM would imply the difficulty to estimate Chl_a and CDOM in near-shore waters where the variability in SPM would dominate the variability in R _rs . Clearly, the match-up statistics for SPM was better with R²=0.73 and 0.87 for two evaluated algorithms, although GOCI-derived SPM overestimated low concentration and underestimated high concentration. Based on this initial match-up analysis, we made several recommendations -1) to collect more offshore under-water measurements of the R _rs data, 2) to include quality flags in level-2 products, 3) to introduce an ISRD correction in the GOCI processing chain, 4) to investigate other types of in-water algorithms such as semianalytical ones, and 5) to investigate vicarious calibration for GOCI data and to maintain accurate and consistent calibration of field radiometric instruments.