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洱海沉积物有色可溶性有机物(CDOM)三维荧光空间分布特性及指示意义 总被引：1，自引：0，他引：1
采用荧光光谱区域体积积分法定量研究洱海沉积物有色可溶性有机物（CDOM）三维荧光空间分布特性，结果表明，洱海沉积物CDOM中类腐殖酸组分占比最高（44.5%~74.2%），其次为溶解性微生物代谢产物（10.7%~20.4%）和类富里酸物质（8.19%~19.7%），而类蛋白组分占比最低，类腐殖酸占比与H/C和N/C均呈显著负相关；南部湖心平台区域沉积物类富里酸和类蛋白组分占比较高，其CDOM自生源占比较高；北部水生植物分布区溶解性微生物代谢产物占比较高，CDOM陆源性较强；中部深水区及南北湖湾区域类腐殖酸占比较高，随水深增加沉积物CDOM自生源特征增强.随沉积物深度增加类腐殖酸和溶解性微生物代谢产物占比呈下降趋势，类富里酸占比呈上升趋势，CDOM自生源特征增强，脂肪化程度增高.随湖泊富营养化程度增加沉积物CDOM受微生物代谢产物影响增强，陆源性增加，而自生源性降低，湖泊沉积物CDOM具有富营养化指示意义. 相似文献
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长江口盐度梯度下不同形态碳的分布、来源与混合行为 总被引：1，自引：0，他引：1
河口碳的生物地球化学过程是全球碳循环的重要组成。通过测定溶解无机碳（DIC）及其稳定同位素丰度（δ13CDIC），溶解有机碳（DOC），有色溶解有机物（CDOM），颗粒有机碳（POC）及其稳定同位素丰度（δ13CPOC）与元素比值（N/C）及相关指标，研究了2014年7月长江口盐度梯度下不同形态碳的分布、来源和混合行为。结果表明，DIC浓度、DOC浓度、POC含量分别为1 583.2~1 739.6 μmol/L，128.4~369.4 μmol/L和51.2~530.8 μmol/L，这些不同形态碳及CDOM的荧光组分的分布模式相似，均是从口内到口外，整体呈现先增大后减小的趋势，并与盐度呈现非保守混合行为。添加作用主要发生在在口门处最大浑浊带附近。与含量相反，从口内到口外，δ13CDIC和δ13CPOC均呈现逐渐减小再增大的趋势，在口门附近达到最低值，分别为-9.7‰和-26.7‰。在口门附近不同形态碳含量上升及δ13CDIC、δ13CPOC的降低可能主要与沉积物再悬浮及微生物作用有关。基于蒙特卡洛模拟的三端元混合模型的结果显示，河口内外POC来源变化明显，口内POC以陆源有机碳贡献为主，平均为62.3%，口外海源贡献逐渐增加。CDOM相关参数结果表明长江口CDOM主要来自陆源输入，海源及人类活动等也对其产生影响。 相似文献
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根据2017年7月和9月在山东威海褚岛北部海域现场测量的COD_(Mn)(Chemical oxygen demand)值和水体表观光学量,结合COMS(Communication,OceanMeteorological Satellite)上搭载的传感器GOCI(Geostationary Ocean Color Imager)所提供的有色可溶性有机物(Chromophoric dissolved organic matter,CDOM)产品,利用星地同步观测数据对现有的基于遥感反射比反演CDOM的模式进行验证,确定适合该海域的CDOM浓度遥感反演模式;通过对测试海域化学需氧量与遥感反演的水体CDOM浓度相关性分析,建立利用CDOM反演COD_(Mn)的遥感模式,并将该模式应用于测试海域LANDSAT 8/OLI(Operational Land Imager)遥感图像上,获取该海域COD_(Mn)浓度专题图,基于这些专题图分析了测试海域COD_(Mn)时空分布特征。结果表明:(1)基于GOCI产品的CDOM浓度值随时间和站点动态变化大,离岸越近数值越高,同一地点水体前后相差近1 h的数值变化也较大;(2)基于LANDSAT 8/OLI遥感数据反演的COD_(Mn)浓度时间动态变化大,总体来看褚岛附近水体的COD_(Mn)含量相对较低,褚岛以北海域水体COD_(Mn)含量有所增加,褚岛西侧水体的COD_(Mn)含量较东侧水体COD_(Mn)含量来说整体偏高。 相似文献
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厦门湾有色溶解有机物的光吸收特性研究 总被引：3，自引：0，他引：3
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。 相似文献
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High-resolution measurements of chromophoric dissolved organic matter in the Mississippi and Atchafalaya River plume regions 总被引：4，自引：0，他引：4
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. 相似文献
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Simultaneous acquisition of water samples, radiance and irradiance measurements were carried out from 40 stations in the Mandovi–Zuari estuaries during February to May 2002. From the samples collected, inherent and apparent optical properties (IOP and AOP) such as absorption coefficient (a), upwelling diffuse attenuation coefficient (ku) and subsurface reflectance (R) were derived. Using these optical properties, radiative transfer at each water column is examined. On the basis of the radiative transfer outcome, band-ratio algorithms are derived for three optically active substances (OAS), viz, chlorophyll-a, suspended sediment and coloured dissolved organic matter (CDOM). The respective algorithms are 670/555, 490/670 and 412/670 nm for chlorophyll-a, suspended sediment and CDOM. These algorithms are applied to Ocean Colour Monitor (OCM), onboard Indian Remote Sensing Satellite (IRS)-Polar Satellite Launch Vehicle (P4), scenes (digital data), to synoptically analyze these OAS. The synoptic analysis of OAS revealed different hydrodynamic characteristics of the estuaries during non-monsoon seasons. 相似文献
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Coloured dissolved organic matter (CDOM) in Southern North Sea waters: Optical characterization and possible origin 总被引：1，自引：0，他引：1
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, aCDOM(375), and the slope of the absorption curve, S. aCDOM(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 aCDOM(375) and S variations evidenced different origins of CDOM in the BCZ. The Scheldt estuarine waters showed decreasing aCDOM(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 aCDOM(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 aCDOM(375) and the decay phase characterized by low S (∼0.013 nm−1) and high aCDOM(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. 相似文献
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Apparent oxygen utilization (AOU), dissolved organic carbon (DOC), coloured dissolved organic matter (CDOM) absorption spectra, and CDOM fluorescence characteristic of aromatic amino acids (excitation/emission 280 nm/320 nm; F(280/320)) and marine-humic like substances (320 nm/410 nm; F(320/410)) were measured in full depth during a cruise in the temperate Eastern North Atlantic (ENA). An optimum multi-parameter (OMP) inverse method was run to calculate water mass proportion-weighted average (archetypal) concentrations of these chemical parameters for all water masses and samples. Archetypal concentrations retain the variability due to water mass mixing and basin scale mineralization from the water mass formation sites to the study area. Conversely, the difference between measured and archetypal concentrations, retain the variability due to dissimilarities in mineralization processes within the study area. Our analysis indicates that DOC supported 26±3% of the AOU in the dark temperate ENA and that basin scale processes occurring at and from the formation area of the water masses explained 63% of the total DOC variability. Our data also suggests that DOC remineralized at the basin scale was of lower molecular weight, and with a lower proportion of fluorescent aromatic amino acids than found within the study area. The relationship between the absorption coefficient at 254 nm (aCDOM(254)) and AOU indicates that aCDOM(254) was consumed during organic matter remineralization in the dark ocean, with 55% of the variability being explained by basin scale processes. The relationships of F(320/410) with AOU and DOC confirmed that marine humic-like substances are produced by microbial degradation processes, at a rate of 6.1±0.9×10−3 mg equivalents of QS mol AOU−1. Our results also indicate that basin-scale remineralization processes account for 85% of the total variability of F(320/410), emphasizing that large scale processes control the formation of humic-like substance in the dark ENA. 相似文献