秋季胶州湾有色溶解有机物荧光特性研究及其来源分析

利用三维荧光光谱(EEMs)-平行因子分析(PARAFAC)技术研究了秋季胶州湾有色溶解有机物(CDOM)的荧光成分组成、分布特征及来源。PARAFAC模型解析出胶州湾CDOM由2类5个荧光组分组成,即类腐殖质成分C1(355nm/430nm)、C2(320nm/390nm)、C3(380nm/465nm)、C4(420(330)nm/505nm)及类蛋白质成分C5(280/325nm)。类腐殖质成分C1、C2、C3和C4的平面分布模式基本一致,呈现由近岸海域向湾中心海域逐渐减小的趋势,而类蛋白质成分C5则是由湾东北部近岸海域向西南部海域呈逐渐减小的趋势。分析表明,秋季胶州湾CDOM类腐殖质成分C1、C2、C3和C4的主要来源为陆源输入,而类蛋白质成分C5主要受城市排污的影响。系统聚类分析表明,以团岛南端和红岛西侧连线为界,所有采样站位被分为两类,分界线西部区域站位CDOM各荧光成分相对含量分别为C1:31.8%~35.5%,C2:30.3%~33.7%,C3:17.1%~20.2%,C4:4.5%~5.2%,C5:9.6%~12.5%;分界线东部区域站位CDOM各荧光成分相对含量分别为C1:30.6%~34.6%,C2:28.8%~32.7%,C3:17.0%~19.1%,C4:3.3%~4.8%,C5:12.1%~18.2%。西部区域CDOM具有较高的C4含量和较低的C5含量,大沽河等河流的陆源输入特征明显,而东部区域CDOM则具有较高的C5含量和较低的C4含量,反映该区域受城市排污影响显著。另外,秋季胶州湾CDOM的HIX范围为1.8~3.2之间,较小的腐殖化因子值反映了秋季胶州湾CDOM的腐殖化程度高较低,在环境中存在时间较短。     

莱州湾沉积物有机质来源

应用C/N、δ13C、δ15N解析了莱州湾沉积物有机质来源,发现湾内有机质主要存在海洋、河口浮游植物以及陆地有机质3种来源。通过C/N、δ13C定量示踪,发现海洋浮游植物是湾内沉积物有机质的最主要来源,相对含量在41.6%—58.5%之间。河口浮游植物有机质、陆源有机质相对含量波动较大,分别在3.8%—43.8%、0—53.5%之间。海洋浮游植物有机质在整个海湾都表现出较高含量。近岸河口附近海域往往表现出高含量的河口浮游植物有机质特征,陆源有机质含量较高区域大都集中在黄河口周围海域,高河口浮游植物有机质以及高陆源有机质特征在黄河口周围海域均有出现。     

颗粒态有机物在长江口及其邻近海域的夏季分布和影响因素初析

利用气相色谱法对长江口及其邻近海域的表层颗粒态木质素(p-lignin)进行测定和分析,结合粒度、有机碳(OC%)、叶绿素a(Chl a)、碳稳定同位素(δ13C)等参数研究颗粒态有机物的夏季分布,并对其分布影响因素进行了初步分析。结果表明,悬浮颗粒物粒度组成以粘土和粉砂为主,平均粒径为7.9μm;OC%的值为0.57—7.41%,Chl a的值为0.35—3.71μg/L,δ13C的值为-25.7‰—–16.6‰,在口门外水华站位出现OC%、Chl a和δ13C的最大值,表明浮游生物的现场生产是主要贡献;紫丁香基酚类(S)、香草基酚类(V)和肉桂基酚类(C)8种木质素酚单体的含量Λ8(相对于总有机碳的含量)为0.0406—1.47mg/100mg OC;紫丁香基系列与香草基系列的质量比值(S/V)的分布范围较宽,为0.5—1.6之间,均值为0.8;肉桂基含量与香草基含量比值(C/V)的分布范围为0.02—0.2之间,均值为0.09;香草基酚类的酸醛比值[(Ad/Al)v]在0.24—2.30之间。盐度、总悬浮颗粒物(TSM)浓度是控制长江口内区与邻近海域颗粒态有机物来源与分布差异的重要控制因素,颗粒态木质素在向海输送过程中还会受到矿物组分、生物降解、浮游生物现场生产等各种因素的作用,使其组成成分和性质发生改变。木质素等参数表明最大浑浊带尽管对颗粒态有机物向海输送有改造作用,但是影响区域有限。     

白令海颗粒有机物碳、氮同位素组成及其生物地球化学意义

Stable carbon and nitrogen isotopic composition of particulate organic matter(POM) were measured for samples collected from the Bering Sea in 2010 summer. Particulate organic carbon(POC) and particulate nitrogen(PN) showed high concentrations in the shelf and slope regions and decreased with depth in the slope and basin, indicating that biological processes play an important role on POM distribution. The low C/N ratio and heavy isotopic composition of POM, compared to those from the Alaska River, suggested a predominant contribution of marine biogenic organic matter in the Bering Sea. The fact that δ13C and δ15N generally increased with depth in the Bering Sea basin demonstrated that organic components with light carbon or nitrogen were decomposed preferentially during their transport to deep water. However, the high δ13C and δ15N observed in shelf bottom water were mostly resulted from sediment resuspension.     

桑沟湾及附近海域表层沉积物碳氮同位素分析及有机质来源

Naturally existing stable carbon and nitrogen isotopes are important in the study of sedimentary organic matter sources. To identify the sources of sedimentary organic matter in Sanggou Bay and its adjacent areas, which is characterized by high-density shellfish and seaweed aquaculture, the grain size, organic carbon(OC), total nitrogen(TN), carbon and nitrogen isotopic composition(δ13C and δ15N) of organic matter in the surface sediment were determined. The results showed that, in August, sedimentary OC and TN ranged from 0.17% to 0.76% and 0.04% to 0.14%, respectively. In November, OC and TN ranged from 0.23% to 0.87% and 0.05% to 0.14%, respectively. There was a significant positive correlation between OC and TN(R=0.98, P0.0001), indicating that OC and TN were homologous. In August, the δ13C and δ15N of organic matter varied from-23.06‰ to-21.59‰ and 5.10‰ to 6.31‰, respectively. In November, δ13C and δ15N ranged from-22.87‰ to-21.34‰ and 5.13‰ to 7.31‰, respectively. This study found that the major sources of sedimentary organic matter were marine shellfish biodeposition, seaweed farming, and soil organic matter. Using a three-end-member mixed model, we estimated that the dominant source of sedimentary organic matter was shellfish biodeposition, with an average contribution rate of 65.53% in August and 43.00% in November. Thus, shellfish farming had a significant influence on the coastal carbon cycle.     

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.     

Tracing dissolved organic matter cycling in the eastern boundary of the temperate North Atlantic using absorption and fluorescence spectroscopy

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 (a_CDOM(254)) and AOU indicates that a_CDOM(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.     

江苏平原地区(淮河流域)潜水碘含量控制因素探讨

本文通过工作区潜水碘含量的分布特点,与所处土壤、水文地质条件、地形地貌等一起进行综合分析,对地下水中碘的控制因素有了一个全新的认识:与前人认为地下水中碘的含量与有机质成正比的观点不同的是,本文认为地下水中碘的含量与有机质含量无固定关系,但有机质有助于促进水溶性碘的增加,相似水文地质条件下成正比;地下水径流条件对潜水碘含量影响重大,径流条件较好的丘陵、岗地往往较低,地势低平、径流条件较差的洼地和泛滥沉积区往往为高碘地区;相同水文地质条件下,地下水中的碘含量与土壤中的含量成正比;碘的另一重要特征是在地下水中的浓度较为稳定,随时间、开采而变化不大。     

西藏北部舍索与拉屋铜矿床硫化物铅同位素特征

本文在系统的野外地质工作基础上,对舍索与拉屋矿床的矿石硫化物铅同位素组成进行综合分析,进而示踪其成矿物质来源。结果显示,舍索矿区矿石硫化物铅的206Pb/204Pb值为18.517~18.776,207Pb/204Pb值为15.671~15.756,208Pb/204Pb值为38.955~39.33;拉屋矿区矿石硫化物铅的206Pb/204Pb值为18.651~18.757,207Pb/204Pb值为15.707~15.823,208Pb/204Pb值为39.183~39.561。研究表明,舍索与拉屋矿床矿石硫化物铅同位素含量比值具有明显的上地壳特征,指示两个矿床成矿物质主要来自上地壳。其中舍索矿床成矿物质富集受燕山期岩浆作用影响,而拉屋矿床部分成矿物质由晚石炭纪地幔物质的喷流沉积作用提供。