长江口及其邻近海域CDOM光谱吸收特性分析

研究了长江口及其邻近海域有色可溶性有机物(CDOM)的光吸收特性,分析了CDOM浓度(吸收系数a(440))、光谱斜率(S_g)与盐度的关系。结果表明:长江口及其邻近海域CDOM的a(440)变化范围为0.21~0.85 m^-1,平均值为0.44 m^-1;S_g值的范围为0.013 3~0.016 7 nm^-1,平均值为0.014 nm^-1;a(440)的水平分布表现为长江口海区比外海区高,S_g的水平分布表现为长江口海区比外海区低,反映了长江口海区CDOM中的腐殖酸成分比外海区大。研究区内a(440)与盐度、S_g与盐度明显线性相关,表明CDOM在河口混合行为中呈保守行为,CDOM具有良好的保守性质。     

西太平洋冬季上层水体有色溶解有机物的分布和转化特征

为深入解析西太平洋溶解有机碳的生物地球化学过程,本研究于2015年12月至2016年1月,开展了西太平洋上层水体有色溶解有机物（CDOM）吸收光谱和荧光光谱特征研究。研究结果表明,西太平洋上层水体CDOM吸收系数a（320）变化范围为0.01~1.07 m-1,平均值为0.18 m-1;其较高值位于100~200 m水层,表层的海水相对含量较低,主要以有机物的光化学分解为主。采用PARAFAC分析CDOM三维荧光光谱特征,得到1种类腐殖质组分C2（252（310 nm）/405 nm）及2种类蛋白组分C1（224（276 nm）/335 nm）和C3（224（260 nm）/300 nm）,其中类腐殖质荧光组分占总荧光强度的11%~22%,蛋白质荧光组分占总荧光强度的78%~89%,蛋白质荧光中类色氨酸和类络氨酸组分对荧光强度的贡献相当。洋流在大尺度上控制西太平洋CDOM的分布特征,两流交界处和环流形成区域的CDOM相对含量较高,荧光信号较强。西太上层水体CDOM相对含量和荧光信息,与温度、盐度、DO和营养盐等理化因素之间的相关分析结果表明,CDOM主要成分类蛋白质的产生主要受上层水体初级生产过程控制。     

长江口盐度梯度下有色溶解有机物的分布、来源与季节变化

通过测定有色溶解有机物（CDOM）的吸收光谱和荧光光谱研究了2015年3月和7月长江口盐度梯度下CDOM的分布、组成、来源及河口混合行为等。利用激发发射矩阵荧光光谱（EEMs）并结合平行因子分析（PARAFAC）,研究了CDOM的荧光组分特征,共识别出两类4个荧光组分组成,即类腐殖质荧光组分C1（260,375/490 nm）、C2（365/440 nm）、C3（330/400 nm）及类蛋白质荧光组分C4（295/345 nm）。结果表明,3月和7月,4种荧光组分的分布模式与总荧光强度都基本一致:从口内到口外,先升高后降低,且4种组分都在河口呈现不保守混合行为,在最大浑浊带处存在添加过程,达到峰值,在口外有去除过程。3月腐殖化指数HIX范围在1.12~7.19,而7月HIX的范围在0.87~6.71;生物指数BIX在3月范围在0.76~1.11,7月为0.62~1.15,表明3月CDOM的腐殖化程度较7月高,而自生贡献比例较7月略低。3月吸收系数α（355）的平均值为0.55 m-1 ,7月的略高,为0.61 m-1,表明7月长江口CDOM的含量略高。光谱斜率比值S_R的季节性变化不大,都是近岸低,远岸高,表明CDOM的平均分子质量从口内到口外在逐渐增加。     

厦门湾有色溶解有机物的光吸收特性研究

研究了厦门湾九龙江河口区、西海域、同安湾及东侧水道海水中有色溶解有机物(CDOM)的光吸收特性,分析了CDOM的河口行为,并讨论了CDOM光吸收特性与其荧光性质之间的关系。结果表明,厦门湾表层海水CDOM光吸收系数a(355)的水平分布表现为河口区最高、东侧水道最低、西海域和同安湾介于两者之间,底层水a(355)的分布与表层基本相似,表明陆源河流输入是厦门湾CDOM的主要来源;a(355)的垂直分布为表层高于底层,主要受水文和生物因素控制。厦门湾表层水CDOM光谱斜率S的平均值介于0.014—0.018nm-1,但河口低盐度区S值较小,反映陆源腐殖质的影响。a(355)在河口混合中呈保守行为,表明CDOM具有良好的保守性质。CDOM的吸收系数a(355)与其荧光强度之间表现为较好的相关关系,指示可以用灵敏度更高的荧光方法来研究CDOM的分布和行为。     

水体石油类信息遥感提取模式研究

石油类是水体有机污染物中的一种,其对水体吸收系数的影响主要体现在有色可溶性有机物(chromophoric dissolved organic matter,CDOM)的光吸收特性上。在水色遥感领域,CDOM光吸收特性主要用其在参考波段的吸收系数和光谱斜率来表征。利用2008年5月、2009年8月和2010年6月在辽宁省盘锦市辽河油田境内获取的CDOM吸收系数、水体表观光学特性以及石油类污染浓度等试验数据,确定表征石油类污染水体CDOM吸收光谱特性的光谱斜率;根据光谱斜率以及表征CDOM浓度的440 nm参考波段吸收系数,建立遥感反演水体石油类污染浓度的模式,并利用31个野外现场实测值对模式精度进行了验证,结果表明,该模式的相对误差为7%;将该模式应用于国产卫星环境一号遥感数据,获取双台子河及辽东湾近岸水体石油类污染空间分布图。     

西太平洋秋季130°E断面有色溶解有机物的分布特征及光降解行为研究

对2018年秋季西太平洋130°E断面上层水体有色溶解有机物(CDOM)的光学特性及光降解行为进行了研究。结果表明,西太平洋上层水体CDOM的吸收系数a(320)变化范围为0.025～0.64 m?1,平均值为(0.20±0.08) m?1;a(320)在表层相对较低,主要与表层CDOM的光漂白去除有关;在100～200 m水层较高,主要与次表层的生物活动有关。利用三维荧光光谱?平行因子分析技术,识别出两种荧光组分:类酪氨酸组分C1和海洋类腐殖质组分C2。C1主要源于棉兰老冷涡?上升流所带来的营养物质对浮游植物生产活动和微生物活动的促进作用;C2主要源于黑潮所带来的海洋类腐殖的输入。光化学降解实验发现,CDOM吸收值的损失主要发生在紫外波段;光照60 h后,类酪氨酸组分相较于海洋类腐殖质组分更易发生光降解;且光降解是西太平洋海域CDOM的重要去除途径。     

渤海近岸水体有色溶解有机物的光吸收特征及其分布

依据2011-08和2012-05的现场调查资料,分析渤海水体有色溶解有机物(CDOM)的光谱吸收特性,研究其分布变化特征及影响因素。结果表明:渤海水体a_(355)的变化范围为0.38~4.15m~(-1),均值为1.33m~(-1),表现为莱州湾渤海湾辽东湾,春季夏季的时空变化特征;表层海水a_(355)的水平分布基本呈近岸及河口区高、远岸稍低的变化规律。光谱斜率S_(275~295)和S_(350~400)的变化范围分别为0.011~0.074nm~(-1)和0.012~0.195nm~(-1),春季整体高于夏季。光谱斜率比S_R的变化范围为0.25~2.25,平均值为0.88,夏季略高于春季,其中春季渤海湾最高,莱州湾次之,辽东湾最低;夏季则莱州湾高于渤海湾。渤海春季水体CDOM主要来源于生物现场生产和底层沉积物再悬浮释放,夏季则主要受陆源径流输入的影响。不同时空条件下CDOM在咸淡水的混合过程中也有着不同的表现,春季多呈非保守行为;夏季莱州湾呈保守行为,渤海湾则呈非保守行为。     

冬季黄渤海有色溶解有机物的光学特性研究

于2016年1—2月对黄渤海海域的有色溶解有机物(CDOM)进行了现场调查,通过分析CDOM的吸收和荧光特性,研究了CDOM在黄渤海的分布、荧光组分、来源。结果表明:CDOM吸收系数a(355)的水平变化范围为0.21~0.74m-1,呈现出近岸高、远岸低的分布趋势。光谱斜率比SR的水平分布总体呈现多源头、多中心的分布特征。a(355)在35°N断面总体呈现出近岸高、远岸低,表层低、底层高的分布。利用EEMs-PARAFAC对6种组分进行分析:C1(230/295)、C3(260/315)、C6(285(230)/335)为类蛋白质荧光组分,C2(295/485)、C4(305/380)、C5(345(270)/430)为类腐殖质荧光组分。荧光组分在渤海受陆源输入影响较大,水平分布上呈现出渤海的荧光平均值高于黄海的荧光平均值,且呈近岸高、远岸低的分布趋势。     

大连港海域石油类物质比吸收系数特征分析

利用2018年8月25-27日和2019年5月15-17日在辽宁省大连港及周边海域测定的不同站点、不同时刻的遥感反射比R_(rs),以及不同深度的水体吸收系数和石油类物质浓度数据,分析了水体石油类物质比吸收系数a_o*(λ)的光谱变化规律和在参考波段440nm处的比吸收系数a_o*(440)的垂向分布特征;将基于遥感反射比R_(rs)估算有色溶解有机物CDOM(Colored Dissolved Organic Matter)吸收系数和水体油浓度C_o的模型应用于LANDSAT8卫星数据,反演出该海域a_o*(440)和油浓度专题图,并分析了两者的空间分布特征。结果表明:(1)a_o*(λ)的光谱分布特征遵循e指数衰减方程的变化规律;由于潮汐作用的影响,不同来向海水的石油类物质浓度不同,导致不同时刻不同站点的a_o*(λ)的光谱斜率有一定的差异;(2)CDOM与油物质的混合比吸收系数a_(go)*(440)随深度的垂向变化没有明显的规律,这也是由于涨落潮变化使得不同来向的海水组分有差异所致;(3)a_o*(440)水平变化具有明显的规律;在石油污染浓度C_o高的海域,a_o*(440)呈现低值,在C_o低的海域,a_o*(440)呈现高值。     

应用CDOM光学特性估算水体COD——以辽宁省盘锦市双台子河和辽东湾为例

有色可溶性有机物(chromophoric dissolved organic matter,CDOM)是水体中一类重要的光吸收物质,在水色遥感中,其光学特性主要以440 nm处的吸收系数和光谱斜率来表征,利用这些光学特性进行水环境要素遥感反演具有较广泛的应用前景.化学需氧量(chemical oxygen deman...     

南黄海和珠江口海区非色素颗粒物光谱吸收特性

文章对南黄海(ST03)和珠江口(ST07)海区不同季节的非色素颗粒物吸收光谱数据进行分析,通过分析404个站位的实测数据,得到非色素颗粒物吸收光谱的特点,结果显示两个海区夏季测量的吸收系数在特征波段(440 nm)的吸收值均小于其他季节测量的吸收值。同时,对非色素颗粒物吸收光谱经验斜率进行分析,ST03夏季Sd=0.009 1 nm-1(标准偏差=0.000 8 nm-1),ST03春季Sd=0.009 6 nm-1(标准偏差=0.000 7 nm-1),ST07夏季Sd=0.008 3 nm-1(标准偏差Sd=0.001 8 nm-1),ST07冬季Sd=0.009 7 nm-1(标准偏差=0.000 9 nm-1)。对获取的经验斜率进行验证,评价其在同一海区不同季节的适应性,结果显示经验斜率的应用效果良好。     

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.     

用三维荧光光谱-平行因子分析法研究长江口南部有色溶解有机物荧光的季节变化

The southern Changjiang River Estuary has attracted considerable attention from marine scientists because it is a highly biologically active area and is biogeochemically significant.Moreover,land-ocean interactions strongly impact the estuary,and harmful algal blooms(HABs) frequently occur in the area.In October 2010 and May 2011,water samples of chromophoric dissolved organic matter(CDOM) were collected from the southern Changjiang River Estuary.Parallel factor analysis(PARAFAC) was used to assess the samples' CDOM composition using excitation-emission matrix(EEM) spectroscopy.Four components were identified:three were humic-like(C1,C2 and C3) and one was protein-like(C4).Analysis based on spatial and seasonal distributions,as well as relationships with salinity,Chl a and apparent oxygen utilization(AOU),revealed that terrestrial inputs had the most significant effect on the three humic-like Components C1,C2 and C3 in autumn.In spring,microbial processes and phytoplankton blooms were also important factors that impacted the three components.The protein-like Component C4 had autochthonous and allochthonous origins and likely represented a biologically labile component.CDOM in the southern Changjiang River Estuary was mostly affected by terrestrial inputs.Microbial processes and phytoplankton blooms were also important sources of CDOM,especially in spring.The fluorescence intensities of the four components were significantly higher in spring than in autumn.On average,C1,C2,C3,C4 and the total fluorescence intensity(TFI) in the surface,middle and bottom layers increased by123%–242%,105%–195%,167%–665%,483%–567% and 184%–245% in spring than in autumn,respectively.This finding corresponded with a Chl a concentration that was 16–20 times higher in spring than in autumn and an AOU that was two to four times lower in spring than in autumn.The humification index(HIX) was lower in spring that in autumn,and the fluorescence index(FI) was higher in spring than in autumn.This result indicated that the CDOM was labile and the biological activity was intense in spring.     

Light absorption by phytoplankton,non-algal particles and dissolved organic matter at the Patagonia shelf-break in spring and summer

Satellite image studies and recent in situ sampling have identified conspicuous phytoplankton blooms during spring and summer along the Patagonia shelf-break front. The magnitudes and spectral characteristics of light absorption by total particulate matter (phytoplankton and detritus) and colored dissolved organic matter (CDOM) have been determined by spectrophotometry in that region for spring 2006 and late summer 2007 seasons. In spring, phytoplankton absorption was the dominant optical component of light absorption (60–85%), and CDOM showed variable and important contributions in summer (10–90%). However, there was a lack of correlation between phytoplankton biomass (chlorophyll-a concentration or [chl a]) and the non-algal compartment in both periods. A statistically significant difference was found between the two periods with respect to the CDOM spectral shape parameter (S_cdom), with means of 0.015 (spring) and 0.012 nm^?1 (summer). Nonetheless, the mean S_cdm values, which describe the slope of detritus plus CDOM spectra, did not differ between the periods (average of 0.013 nm^?1). Phytoplankton absorption values in this work showed deviations from mean parameterizations in previous studies, with respect to [chl a], as well as between the two study periods. In spring, despite the microplankton dominance, high specific absorption values and large dispersion were found (a*_ph(440)=0.04±0.03 m² mg [chl a]^?1), which could be attributed to an important influence of photo-protector accessory pigments. In summer, deviations from general trends, with values of a*_ph(440) even higher (0.09±0.02 m² mg [chl a]^?1), were due to the dominance of small cell sizes and also to accessory pigments. These results highlight the difficulty in deriving robust relationships between chlorophyll concentration and phytoplankton absorption coefficients regardless of the season period. The validity of a size parameter (S_f) derived from the absorption spectra has been demonstrated and was shown to describe the size structure of phytoplankton populations, independently of pigment concentration, with mean values of 0.41 in spring and 0.72 in summer. Our results emphasize the need for specific parameterization for the study region and seasonal sampling approach in order to model the inherent optical properties from water reflectance signatures.     

Gaussian decomposition and component pigment spectral analysis of phytoplankton absorption spectra

The absorption spectrum of phytoplankton is an important bio-optical parameter for ocean color hyperspectral remote sensing;its magnitude and shape can be aff ected considerably by pigment composition and concentration. We conducted Gaussian decomposition to the absorption spectra of phytoplankton pigment and studied the spectral components of the phytoplankton, in which the package effect was investigated using pigment concentration data and phytoplankton absorption spectra. The decomposition results were compared with the corresponding concentrations of the five main pigment groups (chlorophylls a , b , and c , photo-synthetic carotenoids (PSC), and photo-protective carotenoids (PPC)). The results indicate that the majority of residual errors in the Gaussian decomposition are <0.001 m^-1 , and R 2 of the power regression between characteristic bands and HPLC pigment concentrations (except for chlorophyll b) was 0.65 or greater for surface water samples at autumn cruise. In addition, we determined a strong predictive capability for chlorophylls a , c , PPC, and PSC. We also tested the estimation of pigment concentrations from the empirical specific absorption coeffi cient of pigment composition. The empirical decomposition showed that the Ficek model was the closest to the original spectra with the smallest residual errors.The pigment decomposition results and HPLC measurements of pigment concentration are in a high consistency as the scatter plots are distributed largely near the 1:1 line in spite of prominent seasonal variations. The Wozniak model showed a better fit than the Ficek model for Ch1 a , and the median relative error was small. The pigment component information estimated from the phytoplankton absorption spectra can help better remote sensing of hyperspectral ocean color that related to the changes in phytoplankton communities and varieties.