Organic and inorganic matter in Louisiana coastal waters: Vermilion, Atchafalaya, Terrebonne, Barataria, and Mississippi regions

Chromophoric dissolved organic matter (CDOM) spectral absorption, dissolved organic carbon (DOC) concentration, and the particulate fraction of inorganic (PIM) and organic matter (POM) were measured in Louisiana coastal waters at Vermilion, Atchafalaya, Terrebonne, Barataria, and Mississippi River locations, in 2007-2008. The range of CDOM was 0.092 m⁻¹ at Barataria in June 2008 to 11.225 m⁻¹ at Mississippi in February 2008. An indicator of organic matter quality was predicted by the spectral slope of absorption coefficients from 350 to 412 nm which was between 0.0087 m⁻¹ at Mississippi in May 2008 and 0.0261 m⁻¹ at Barataria in June 2008. CDOM was the dominant component of light attenuation at Terrebonne and Barataria. Detritus and CDOM were the primary components of light attenuation at Vermilion, Atchafalaya, and Mississippi. DOC ranged between 65 and 1235 μM. PIM ranged between 1.1 and 426.3 mg L⁻¹ and POM was between 0.3 and 49.6 mg L⁻¹.     

太湖冬季有色可溶性有机物吸收荧光特性及遥感算法

基于2006年和2007年1月两次太湖采样,对50个点位的有色可溶性有机物(CDOM)光谱吸收、荧光、溶解性有机碳(DOE)浓度及遥感反射率进行测定与分析,探讨冬季太湖CDOM的吸收荧光特性及空间分布,建立CDOM吸收系数的遥感反演算法.结果表明,太湖冬季CDOM在355nm处吸收系数a(355)变化范围和均值分别为1...     

淮河流域周村水库夏季CDOM吸收光谱特征、空间分布及其来源分析

基于2015年8月采集的24个淮河流域以周村水源水库为代表的表层水样的有色溶解性有机物(CDOM)吸收系数数据,研究了CDOM吸收光谱的空间分布特征,考察了CDOM的吸收系数与水质参数的相关关系,同时探讨了周村水库夏季CDOM的潜在来源.结果显示:依据CDOM的吸收光谱空间分布特性及采样点分布特征,周村水库分为入库口、过渡区和主库区3个特征水域;CDOM的吸收系数沿入库口到主库区依次递减,S值呈现相反的趋势;分析发现S240~500与a(355)和a*(355)呈极显著负相关(R~2=0.98、0.88);CDOM吸收系数a(355)与溶解性有机碳(DOC)浓度具有良好的线性相关,有利于建立DOC遥感反演模型;同时,CDOM吸收系数a(355)与a_(ph)(440)存在极显著正线性相关,表明浮游植物的新陈代谢及其降解产物是夏季周村水库CDOM的潜在来源.综上,通过对夏季周村水库水体CDOM的研究,丰富了关于水源水体CDOM的调查资料,可为日后水库的管理提供技术支撑.     

基于CDOM吸收特性的东北地区水库DOC浓度遥感估算

有色溶解性有机物(CDOM)广泛存在于水体中,占溶解有机碳(DOC)10%～90%,其浓度影响水环境碳循环过程、污染物质迁移以及水生生物群落的结构和功能。为分析东北地区水库DOC碳循环情况,本文于2015—2020年对第二松花江流域典型水库白山水库和丰满水库进行5次现场观测和室内实验,在分析CDOM吸收特性的基础上,基于Landsat系列卫星利用波段比值法建立CDOM浓度反演模型(R²=0.82),根据实测值CDOM与DOC的强相关性(R²=0.78),进而估算水库DOC浓度。结果表明：(1)利用野外实测数据和Landsat系列卫星能够对东北内陆水库CDOM浓度进行良好反演,(2)2000—2020年白山水库和丰满水库年际CDOM和DOC浓度变化不大,在2010年之后表现出轻微上升趋势,CDOM浓度从支流和干流的汇入到主库区呈现逐渐减少趋势,(3)白山水库和丰满水库M值(CDOM在250和365 nm处吸收系数比值)和S_275～295(CDOM在275～295 nm波段处的吸收光谱的斜率)较小、SUVA_254<...     

Origin of Dissolved Organic Carbon Studied by UV‐vis Spectroscopy

Dissolved organic carbon (DOC) distributions in water from Lake Ipê, MS, Brazil, were investigated. The samplings were performed monthly (surface, 1 m depth, and bottom) from June 1999 to June 2000. Absorbance at 285 nm and DOC concentrations in mg dm^—3, p(DOC), were highly correlated for the three depths. 77% of the surface, 85% for 1 m and bottom samples presented a variation between 20 dm³ g^—1 cm^—1 and 50 dm³ g^—1 cm^—1 of A(285 nm)/p(DOC), that characterizes the dissolved organic matter in lake water as essentially fulvic. The ratio A(254 nm)/p(DOC) was also sensitive for fulvic matter, and an A(250 nm)/A(365 nm) = 4 ratio was characteristic of strongly colored waters. The ratios A(436 nm)/p(DOC) for the three depths also showed a significant correlation. The predominance of fulvic acid is explained by environmental characteristics such as the tropical climate, temperatures above 18 °C, and the lake environment. It was demonstrated that the variation in the water carbon content due to different compartments in the lake can be monitored by UV‐vis spectroscopy ratios.     

抚仙湖秋、冬季光衰减特征及其与有色可溶性有机物的关系

为了研究抚仙湖紫外辐射(UVR)和光合有效辐射(PAR)衰减的时空特征及其与有色可溶性有机物(CDOM)、悬浮物(SS)、浮游植物(叶绿素a表征)等因子的关系,于2014年10月(秋季)、2015年1月(冬季)开展现场调查,结果显示:秋季不同波长(段)的漫射衰减系数Kd(305)、Kd(340)和Kd(PAR)分别为1.27±0.12、0.68±0.11和0.32±0.13 m-1,冬季分别为1.13±0.10、0.63±0.07和0.36±0.07 m-1;秋季CDOM的不同波长吸收系数ag(254)、ag(305)和ag(340)分别为4.09±0.26、1.18±0.09和0.57±0.05 m-1,冬季分别为2.95±0.24、0.61±0.11和0.11±0.07 m-1,秋季ag(254)、ag(305)和ag(340)显著高于冬季;秋季Kd(305)显著大于冬季,这与秋季(雨季)较高的CDOM丰度、浮游植物生物量(及SS浓度)有关.秋季ag(305)/Kd(305)、ag(340)/Kd(340)均显著高于冬季;秋季及秋冬季整体而言,ag(254)与Kd(305)、Kd(340)呈显著正相关,各多元逐步回归方程中均包含ag(254),说明CDOM吸收对UVR的衰减有重要贡献.空间差异方面,秋季北部的ag(254)、Kd(305)和Kd(340)显著高于南部,冬季南北部无明显差异,或与雨旱季北岸河流输入的CDOM和SS的情况有关.此外,浮游植物对UV-B衰减的影响和SS(与CDOM的交互作用)对UV-A衰减的影响更在于季节变化方面,而影响UVR、PAR衰减的各因子的相对贡献有待进一步量化.     

官厅水库秋季悬浮颗粒物和CDOM吸收特性

利用2012年9月5日在官厅水库采集的水体吸收系数数据,对总悬浮颗粒物、浮游植物色素颗粒物、非色素颗粒物和有色可溶性有机物的吸收特性进行研究.结果表明:秋季官厅水库的颗粒物吸收以浮游植物色素吸收为主,总颗粒物吸收光谱与浮游藻类吸收光谱相似;非色素颗粒物和有色可溶性有机物的吸收系数随波长的增大接近指数规律衰减;a_d(440)、a_d(675)与C_Chl.a呈显著相关,表明官厅水库秋季的非色素颗粒物主要来源于浮游藻类降解产物,陆源性输入较少;a ph(440)、a ph(675)与C_Chl.a存在显著线性关系,但其比吸收系数较为恒定,与C_Chl.a基本无关;不同采样点的不同组分吸收系数对总吸收系数的贡献不同,大致有4种表现类型.在富营养程度较高的妫库区,浮游植物色素是水体光谱吸收的主导因子;在富营养程度较低的中库区,颗粒物与有色可溶性有机物共同主导水体光谱吸收.     

兴凯湖春季水体悬浮颗粒物和CDOM吸收特性

为了分析兴凯湖水体光学活性物质的吸收特性、来源和空间分布以及对400~700 nm范围内总吸收的贡献,于2013年5月对该水体进行野外实验,对水体中浮游藻类、非藻类颗粒物和有色可溶性有机物的吸收特性和水质参数进行测定.结果表明:总悬浮颗粒物的吸收光谱与非藻类颗粒物相似,色素颗粒物含量较少且单一,非藻类颗粒物在总悬浮颗粒物吸收中占主导地位,其贡献率始终在50%以上.CDOM吸收曲线的拟合函数斜率值Sg均高于其它水体.440 nm处总悬浮颗粒物和非藻类颗粒物的吸收系数ap(440)、ad(440)与总悬浮颗粒物、无机悬浮颗粒物和有机悬浮颗粒物浓度相关性均较好,与叶绿素a(Chl.a)浓度的相关性较差.兴凯湖与其它Ⅱ类水体的差异性表现在440 nm处CDOM吸收系数ag(440)与Chl.a浓度、溶解性有机碳(DOC)浓度均无显著相关性,说明DOC以无色部分为主.总体上,大兴凯湖各吸收系数和水质参数均值均低于小兴凯湖,后者水质受农耕区退水及周围渔业、旅游业的影响较大.     

青藏高原典型湖库光学吸收特性与光合有效辐射衰减系数初步研究

青藏高原地区分布的湖泊数量众多、面积较大、分布范围广泛.受制于恶劣的自然条件,对该地区湖泊的光学吸收特性以及光合有效辐射衰减系数(Kd(PAR))的研究鲜有成果.本文依据2014和2015年间采集的13个典型高海拔、湖泊面积较大的湖库的现场实测数据和实验室测定数据,分析了采样湖库各个采样点的Kd(PAR)特征以及有色可溶性有机物(CDOM)、藻类颗粒物吸收及非色素颗粒物吸收特性,计算并分析了Kd(PAR)与透明度以及光学活性物质的关系.研究结果表明:青藏高原地区各湖库平均各项颗粒物吸收系数均较低,总颗粒物吸收系数在400~700 nm波段内不超过0.14 m~(-1)、CDOM吸收系数在355 nm波长处最高,为1.23 m~(-1)、最低接近于0、藻类颗粒物吸收特性不明显;实验数据完整的巴木错、格仁错和班公错的主导吸收组分各异,其中巴木错为CDOM吸收主导,格仁错与班公错为非色素颗粒物吸收主导;青藏高原采样湖泊总体Kd(PAR)平均值较小,仅为0.26 m~(-1),样点最大值出现在可鲁克湖(1.17 m~(-1)),最小值出现在普莫雍错(0.10 m~(-1));在采样湖泊中Kd(PAR)与透明度呈显著相关;Kd(PAR)与CDOM的相关性最强,叶绿素a浓度次之,与总悬浮颗粒物浓度的相关性最不显著.     

抚仙湖有色可溶性有机物的来源组成与时空变化

基于2017年1-12月在抚仙湖开展的逐月观测,利用紫外-可见吸收光谱和三维荧光光谱技术探讨该湖有色可溶性有机物（CDOM）的来源组成及时空变化特征.12个月CDOM吸收值a（254）的均值为3.47±0.57 m^-1,范围为1.82~5.22 m^-1,说明CDOM丰度较低.平行因子分析结果给出了2种类酪氨酸荧光组分（C1和C3）、1种类色氨酸荧光组分（C2）、1种类腐殖质荧光组分（C4）,12个月内源组分（C1+C3）对总荧光强度的平均贡献为65.81%±15.38%,外源组分（C2+C4）的平均贡献为34.19%±15.38%;荧光指数FI的均值为1.73±0.14,腐殖化指数HIX的均值为1.02±0.37,生源化指数BIX的均值为1.23±0.27,说明CDOM主要为微生物内源产生.时空变化方面,春（3-5月）、夏（6-8月）、秋（9-11月）和冬（1、2、12月）季的a（254）分别为3.20±0.47、3.76±0.64、3.67±0.50和3.23±0.38 m^-1,夏季和秋季均显著高于冬季和春季;CDOM丰度及内外源组分的空间分布具有季节异质性,可能与流域土地利用、河流输入、降雨、温度、光辐射等因素有关.     

Variations in light absorption properties during a phytoplankton bloom in the Pearl River estuary

From 15 to 28 August in 2007, a Chaetoceros socialis bloom was detected in the Pearl River Estuary water with chlorophyll a concentration (Chl a) up to 30 mg m⁻³ and cell density up to 10⁶ cells L⁻¹. Time series of bio-optical measurements was obtained at a single site (114.29°E, 22.06°N) with the mooring of marine optical buoy. Light absorption properties of seawater experienced large variability throughout the algal bloom. Absorption by colored dissolved organic matter (CDOM) was one of the dominant optical components of the light absorption (30–70%) especially for pre- and post-bloom waters, and it tended to decrease with Chl a during the algal bloom. Absorption by phytoplankton was another dominant optical component (18–50%) and increased rapidly with Chl a. Phytoplankton and accompanying material played dominant roles in light absorption as indicated by the relationship between absorption coefficient and Chl a. At high pigment concentrations, water samples showed significantly lower specific phytoplankton absorption, compared with pre- and post-bloom conditions, with the specific phytoplankton concentration at 443 nm varied between 0.011 and 0.022 m² mg⁻¹ and that at 676 nm between 0.007 and 0.018 m² mg⁻¹; small values of blue-to-red ratio of phytoplankton were also observed. These lower values were associated with variations in phytoplankton size structure. Spectral variability of phytoplankton absorption and total absorption (not including the fixed background absorption by pure water itself) could be expressed as simple linear functions linking absorption at one wavelength to the absorption at the other wavelengths, with the slope of the relationship changing with wavelength. The absorption coefficients by non-algal particles and CDOM follow the general exponential functions with remarkably limited variability in the exponent with means of 0.0105 and 0.0166 nm⁻¹, respectively. These spectral dependencies of absorption coefficients provide useful information for retrieving inherent optical properties from reflectance data in a remote-sensing context.     

Seasonal controls on DOC dynamics in nested upland catchments in NE Scotland

Spatial and temporal variability of hydrological responses affecting surface water dissolved organic carbon (DOC) concentrations are important for determining upscaling patterns of DOC export within larger catchments. Annual and intra‐annual variations in DOC concentrations and fluxes were assessed over 2 years at 12 sites (3·40–1837 km²) within the River Dee basin in NE Scotland. Mean annual DOC fluxes, primarily correlated with catchment soil coverage, ranged from 3·41 to 9·48 g m^?2 yr^?1. Periods of seasonal (summer–autumn and winter–spring) DOC concentrations (production) were delineated and related to discharge. Although antecedent temperature mainly determined the timing of switchover between periods of high DOC in the summer‐autumn and low DOC in winter‐spring, inter‐annual variability of export within the same season was largely dependent on its associated water flux. DOC fluxes ranged from 1·39 to 4·80 g m^?2 season^?1 during summer–autumn and 1·43 to 4·15 g m^?2 season^?1 in winter–spring.Relationships between DOC areal fluxes and catchment scale indicated that mainstem fluxes reflect the averaging of highly heterogeneous inputs from contrasting headwater catchments, leading to convergent DOC fluxes at catchment sizes of ca 100 km². However, during summer–autumn periods, in contrast to winter–spring, longitudinal mainstem DOC fluxes continue to decrease, most likely because of increasing biological processes. This highlights the importance of considering seasonal as well as annual changes in DOC fluxes with catchment scale. This study increases our understanding of the temporal variability of DOC upscaling patterns reflecting cumulative changes across different catchment scales and aids modelling of carbon budgets at different stages of riverine systems. Copyright © 2010 John Wiley & Sons, Ltd.     

Behaviour of Different Molecular-weight Fractions of DOC of Elbe River Water during River Bank Infiltration

This paper reports changes in dissolved organic carbon concentration β(DOC) and the relation between UV-active and non-UV-active components determined for Elbe river water and river bank infiltrate in the Torgau river basin between 1992 and 1994. Using an ultrafiltration method, the fractionation of the DOC content was obtained for the fractions > 10 000 g/mol, 1 000…10 000 g/mol, and < 1 000 g/mol. The spectral absorption coefficient at 254 nm a₂₅₄ of the molecular-weight fractions was also measured. The mean total DOC concentration of Elbe river water decreased from 6.0 mg/L to below 3.9 mg/L along two investigated flowpaths. Two thirds of the decrease occurred within the first few metres of the river bed and one third along the 350 m length of the groundwater flowpaths. The a₂₅₄ values showed a significant decrease from 14.8 1/m in Elbe river water to 7.8 1/m in the aquifer. Along a flowpath, the proportion of low-molecular weight fraction of DOC increased, the proportion of high-molecular weight fraction decreased, and the proportion of the 1 000…10 000 g/mol molecular-weight fraction remained relatively stable. The Elbe river water contained the main portion of UV-active compounds in the fraction 1 000…10 000 g/mol, and this was also the case for samples of river infiltrate. For the high-molecular weight fraction, mainly non-UV-active compounds were attenuated in the river bed sediment.     

Hydrograph separation to improve understanding of Dissolved Organic Carbon Dynamics in Headwater catchments

Dissolved organic carbon (DOC) is a key component of the global carbon cycle, but, to date, large uncertainties still exist on its source and fate in first‐order streams. In a 23 ha rangeland and steep‐slope headwater of South Africa, our aim was to quantify the contribution of overland flow (OF), soil water (SW) and ground water (GW) to DOC fluxes (DOC_F), and to interpret the results in terms of DOC sources and fate. The average 2010–2011 DOC concentration (DOC_C) at the catchment outlet was 4.7 mg C l^?1 with a standard error of ±2.5 mg C l^?1, which was significantly lower than in SW (15.2 ± 1.6 mg C l^?1) and OF (11.9 ± 0.8 mg C l^?1), but higher than in GW (2.3 ± 0.6 mg C l^?1). Based on end‐member mixing using Si and Na concentration in the water compartments, the average SW contribution to DOC_F was 66.4%, followed by OF (30.0%) and GW (3.6%). The resulting estimated DOC_F at the catchment outlet was 8.05 g C m² y^?1. This was much higher than the observed value of 2.80 g C m² y^?1, meaning that 5.25 g C m² y^?1 or 65% of the DOC is lost during its downslope and/or downstream transport to the catchment outlet. Complementary investigations revealed that the DOC_C in SW dropped from 15.2 ± 1.6 to 2.6 ± 0.3 mg C l^?1 during its downslope transport to the river system, which corresponded to a net loss of 5.10 g C m² y^?1, or 97% of the catchment DOC losses. These results on DOC sources and potential fate in headwaters are expected to improve our understanding of the impact of hydrology on the global C‐cycle. Copyright © 2013 John Wiley & Sons, Ltd.     

Water balance,nutrient and carbon export from a heath forest catchment in central Amazonia,Brazil

Carbon storage values in the Amazon basin have been studied through different approaches in the last decades in order to clarify whether the rainforest ecosystem is likely to act as a sink or source for carbon in the near future. This water balance, dissolved organic carbon (DOC) and nutrient export study were carried out in a micro‐scale heath forest (Campina) catchment in central Amazonia, Brazil. For a 1‐year study period (18 March 2007 until 19 March 2008), rainfall amounted to 3054 mm; of which, 1532 mm was evaporated by the forest (4.1 mm day^?1). Rainfall interception loss amounted to 15.6% of gross rainfall. Surface runoff amounted to 485 mm, whereas another 1071 mm was discharged as regional groundwater outflow. Accumulated DOC exports in surface runoff amounted to 15.3 g m^?2 year^?1, whereas the total carbon exported was 55.9 g m^?2. This is much higher than that observed for a nearby tall rainforest catchment in central Amazonia (DOC export < 20 g m^?2). As Campina heath forest areas cover a significant proportion of the Amazon Basin, these differences in ecosystem hydrological carbon exports should be taken into account in future studies assessing the carbon budget for the Amazon Basin. Macro‐nutrient exports were low, but those of calcium and potassium were higher than those observed for tall rainforest in the Amazon, which may be caused by a lower retention capacity of the heath forest ecosystem. Copyright © 2015 John Wiley & Sons, Ltd.     

Effect of sediment resuspension on underwater light field in shallow lakes in the middle and lower reaches of the Yangtze River: A case study in Longgan Lake and Taihu Lake

Based on three continuous in situ underwater light field measurement under different wind waves conditions in Longgan Lake, Meiliang Bay of Taihu Lake in July 2003 and littoral zone near TLLER in July 2004, respectively, the effects of sediment resuspension caused by wind waves on PAR diffuse attenuation, absorption coefficients and euphotic depths are analyzed. In Longgan Lake, PAR diffuse attenuation coefficients during small, middle and large wind waves were 1.74, 2.02 and 2.45 m^?1, respectively, and the corresponding PAR spectral diffuse attenuations ranged from 0.98 to 2.97, 1.34 to 3.95 and 1.80 to 5.40 m^?1, respectively. In Meiliang Bay, PAR diffuse attenuation coefficients were 2.63, 3.72, 4.37 m^?1 during small, middle and large wind waves. PAR diffuse attenuation coefficients increased by 41% and 66% from small to middle, large wind waves, respectively. Absorption coefficients integrated over the range of PAR of CDOM, phytoplankton were 0.26, 0.28 m^?1; 0.76, 0.49 m^?1, respectively during middle and large wind waves. Absorption coefficients integrated over the range of PAR of non-algal particulate matter and total suspended particulate matter increased from 0.94 to 1.73 m^?1, and from 1.70 to 2.22 m^?1, respectively during middle and large wind waves. Relative contributions of absorption coefficients of non-algal particulate matter to total absorption coefficient integrated over the range of PAR were 44.14%, 65.05%, respectively, during middle and large wind waves. PAR euphotic depths decreased by 0.40, 0.19, 0.20 m from middle to large wind waves in Longganhu Lake, Meliang Bay and littoral zone near TLLER. Significant correlations were found between transparency, PAR diffuse attenuation coefficients, euphotic depths and total suspended particulate matter, wind velocity, wave height. Most significant correlations were found between transparency, PAR diffuse attenuation coefficients, euphotic depths and inorganic suspended particulate matter but low correlations for chlorophyll a, dissolved organic carbon. Increase of total suspended particulate matter, especially inorganic suspended particulate matter caused by wind waves was the dominant factor affecting underwater light field in shallow lakes in the middle and lower reaches of the Yangtze River based on observations at three stations.     

Distribution and photoreactivity of chromophoric dissolved organic matter in northern Gulf of Mexico shelf waters

The distribution and photoreactivity of chromophoric dissolved organic matter (CDOM) in the northern Gulf of Mexico along the Louisiana coastal shelf were examined during three cruises in summer 2007, fall 2007, and summer 2008. The influence of the Mississippi River plume was clearly evident as CDOM levels (defined as a₃₀₅) and dissolved organic carbon (DOC) concentrations were well-correlated with salinity during all cruises. Elevated CDOM and CDOM:DOC ratios of surface samples collected offshore of Atchafalaya Bay and the Breton-Chandeleur Sound complex indicated emanations of organic-rich waters from coastal wetlands are also an important source to nearshore shelf waters. Generally, CDOM and DOC levels were highest in surface waters and decreased with depth, but during summer 2007 and summer 2008, CDOM levels in near-bottom samples were occasionally higher than at mid-depths without concomitant increases in DOC. CDOM photobleaching was measured during 24 irradiations using a SunTest XLS+ solar simulator with photobleaching rate coefficients (k₃₀₅) ranging from 0.011 to 0.32 h⁻¹. For fall 2007 and summer 2008, higher k₃₀₅ values were generally observed in samples with higher initial CDOM levels. However, samples collected during summer 2007 did not exhibit a similar pattern nor were there differences in photobleaching rates between surface and bottom samples. Spectral slope coefficients (S_275-295 or S_350-400) and DOC levels were largely unchanged after 24 h irradiations. Modeled CDOM photobleaching for northern Gulf of Mexico mid-shelf waters predicts that during the summer when solar irradiance is high and the water column becomes stratified, nearly 90% of the CDOM in the upper 1 m may be lost to photobleaching, with losses up to 20% possible even at 10 m depth.     

Sensitivity analysis of CDOM spectral slope in artificial and natural samples: an application in the central eastern Mediterranean Basin

In the past two decades, optical properties of chromophoric dissolved organic matter (CDOM) in marine environments have been extensively studied. Many of these studies report CDOM properties for the offshore environment where this complex mixture of optically active compounds is strongly diluted. Nevertheless, autochthonous and allochthonous sources have been identified and sinks related to photodegradation and bacterial activity have been demonstrated. The calculation of the spectral slope of the CDOM absorption curve has been proven to be useful and is often reported. However, a rigorous uncertainty analysis of the slope calculation is rarely reported. In this paper, we propose a method to evaluate the uncertainty of CDOM spectral slope calculated between 270 and 400 nm, using both naturally sampled and artificial solutions. We use these results to study the ultra-oligotrophic waters of the Mediterranean Sea (central eastern basin), where little is known about CDOM spatial distribution. We show that dilutions of both artificial and natural samples produce a Gaussian distribution of spectral slopes, indicating that consistent values may be determined, with a typical uncertainty of ±0.0004 nm⁻¹ when absorption at 300 nm was greater then 0.1 m⁻¹ (0.1 m pathlength). Comparing the distribution of spectral slopes from central eastern basin samples to a Gaussian distribution, we show differences between measurements that were significantly different. These values allow us to distinguish possible sources (algal derived CDOM), sinks (e.g. photo-bleaching) at different depths. We propose a subdivision of CDOM compounds into refractory and semilabile/refractory pools and evaluate the CDOM spectral slope of algal derived CDOM released at or near deep chlorophyll maximum.     

龙感湖水体光学特性的观测

基于2002—2003年秋、夏季原位水下光场巡测及连续定点观测资料分析了龙感湖不同湖区及不同风浪条件下水体的光学特性,探讨了光衰减系数、辐照度比的光谱分布、空间差异及不同风浪条件对水下光场的影响.结果表明,水下光谱在紫光波段衰减最强烈,其次是蓝光,红、绿光衰减最弱,并且向下辐照度衰减系数一般要大于向上辐照度衰减系数.秋季L1-L3点向下辐照度400—700nm波段衰减系数的变化范围分别为0.71—3.60、1.06—3.72、0.78—2.89m-1;光衰减系数的空间分布是位于湖中心的12点要略大于两边的L1、L3点;辐照度比的变化趋势极为一致,最低值出现在短波蓝光波段,最高值出现在550—600nm之间;从小风浪到中风浪、大风浪其PAR衰减系数分别是1.74、2.02、2.45m-1;透明度、衰减系数与悬浮物浓度相关性最好,决定系数在0.7以上,但其变化除受悬浮物影响外还要受制于溶解性有机物和浮游植物;440nm波长衰减系数(Kd(440))与悬浮物(SS)、溶解性有机碳(DOC)、叶绿素a(Chl.a)的多元线性回归方程为:Kd(440)=0.514—0.075SS 0.125DOC 0.100Chl.a(R2=0.87,N=8,P≤0.05)