大亚湾颗粒有机物生化组成研究

对大亚湾海域颗粒有机物（ＰＯＭ）的生化组成与环境因子的关系进行了研究。现场采样调查分别于１９９５年５月和１１月进行,研究结果表明,环境因子对ＰＯＭ生化组成有很大的影响。核电站的运作使大亚湾海域有局部升温现象,温度升高,使经类含量升高。蛋白持含量受无机氮盐含量影响显著,由于大亚湾ＰＯＭ中蛋白质的含量不高,而且大亚湾水域呈贫氮特征,适当增加有该海区无机氮的含量对于提高大亚湾ＰＯＭ的生物营养性具有现实意     

九龙江河口区溶解态、颗粒态铀同位素的地球化学行为

对九龙江河口区枯、丰水期水体中溶解态、颗粒态铀同位素地球化学行为的研究表明,溶解态铀与盐度存在良好的正相关关系,证实枯、丰水期该河口区水体中的铀均是保守行为。在低盐度区域（Ｓ＜１０）,~２３８Ｕ主要以颗粒态形式存在,颗粒态~２３８Ｕ所占份额随盐度增加而降低。~（２３８）Ｕ之条件分配系数介于 １． ２ × １０~３～１． ５ ×１０~５ｄｍ~３／ｋｇ之间,它与盐度呈负相关关系,但与悬浮颗粒物浓度无相关关系存在。枯水期悬浮颗粒物上~２３４Ｕ／~２３８Ｕ_Ａ．Ｒ．与盐度的负相关关系为河口区悬浮颗粒物中~２３４Ｕ的优先沥取理论提供了有力的证据。     

Environmental geochemistry of Damodar River basin, east coast of India

 Water and bed sediment samples collected from the Damodar River and its tributaries were analysed to study elemental chemistry and suspended load characteristics of the river basin. Na and Ca are the dominant cations and HCO₃ is the dominant anion. The water chemistry of the Damodar River basin strongly reflects the dominance of continental weathering aided by atmospheric and anthropogenic activities in the catchment area. High concentrations of SO₄ and PO₄ at some sites indicate the mining and anthropogenic impact on water quality. The high concentration of dissolved silica, relatively high (Na+K)/TZ⁺ ratio (0.2–0.4) and low equivalent ratio of (Ca+Mg)/(Na+K) indicate that dissolved ions contribute significantly to the weathering of aluminosilicate minerals of crystalline rocks. The seasonal data show a minimum ionic concentration in the monsoon season, reflecting the influence of atmospheric precipitation on total dissolved solids contents. The suspended sediments show a positive correlation with discharge and both discharge and suspended load reach their maximum value during the monsoon season. Kaolinite is the mineral that is possibly in equilibrium with the water. This implies that the chemistry of the Damodar River water favours kaolinite formation. The concentration of heavy metals in the finer size fraction (<37 μ m) is significantly higher than the bulk composition. The geoaccumulation index values calculated for Fe, Mn, Zn, Ni and Cr are well below zero, suggesting that there is no pollution from these metals in Damodar River sediments. Received: 21 January 1998 · Accepted: 4 May 1998     

新疆博斯腾湖水体颗粒和溶解有机碳的季节变化及其来源初探

在博斯腾湖选取了13个点位,于2012年5、8、10月测定表层和底层水体中的颗粒有机碳、溶解有机碳、颗粒有机氮和叶绿素a含量.结果显示颗粒和溶解有机碳在表层水体中的浓度与底层相近.博斯腾湖水体中颗粒有机碳的季节变化十分明显,其平均浓度从春季(0.64 mg/L)到夏季(0.71 mg/L)变化不大,但在秋季变化十分显著(浓度达1.58 mg/L).其中西北湖区和湖心区颗粒有机碳的季节变化最明显,东部湖区颗粒有机碳的季节变化相对较小.博斯腾湖水体的颗粒有机碳在春、秋两季主要来自外源输入,在夏季受水体中浮游生物的影响较大.博斯腾湖水体中溶解有机碳也具有一定的季节变化,夏季浓度(平均为9.3 mg/L)略低于春、秋两季(平均为10.3 mg/L).溶解有机碳在河口区的季节变化最强,其夏季浓度明显偏低,主要是由于开都河河水的稀释作用.总体上,博斯腾湖水体中溶解有机碳浓度的变化主要受外部因素的影响.     

太湖水体吸收分解(Ⅰ):悬浮颗粒与浮游植物色素的分离

以2008年10月太湖实测数据为基础,用改进的指数函数和线性法拟合非色素颗粒物吸收和浮游植物色素吸收,根据二者的加和关系,建立总悬浮颗粒物吸收分解模型,依据参量的不同,分别构建了两个分解模型(Mod-4和Mod-5),两者都可以较好的分解出太湖水体浮游植物色素吸收和非色素颗粒物吸收,但Mod-5的拟合精度稍高于Mod-4.研究结果对于进一步探索和建立太湖区域生物光学模型,精确反演水质参数具有一定意义.     

因子分析法在水质参数反演中的应用

2008年11月、2009年4月,分别对太湖水体以及2009年6月对巢湖水体进行野外实验.对太湖水体遥感反射率进行因子分析,并利用遥感反射率的不同因子,对叶绿素和总悬浮物浓度进行反演,并对反演因子的普适性进行验证.利用第一因子反演太湖春季叶绿素浓度,平均相对误差为22.1%,均方根误差为3.48g/L,利用该方法反演巢湖、太湖秋季水体的叶绿素浓度没有取得较好的效果;利用第二因子反演太湖春季总悬浮物浓度,平均相对误差为13.9%,均方根误差为11.33mg/L,利用该因子反演巢湖、太湖秋季水体的总悬浮物浓度同样取得较好效果.结果表明:利用遥感反射率的第一因子对叶绿素浓度进行反演,该方法不具有普适性;利用遥感反射率的第二因子对总悬浮物浓度进行反演能取得较好的结果,此方法具有一定的普适性.     

基于叶绿素荧光峰特征的浑浊水体悬浮物浓度遥感反演

内陆水体光学特性复杂,其水质参数遥感反演是当前环境遥感研究的热点与难点.2004年10月在太湖实测了67个站点的遥感反射率与相应站点水质参数浓度,通过对水体反射率光谱的分析发现,秋季太湖悬浮物主导了水体光学特性,叶绿素荧光峰的特征主要体现为悬浮物浓度的变化.据此建立了基于水面实测岛光谱遥感反射率数据的叶绿素荧光峰特征与悬浮物浓度之间的拟合关系,发现二者具有很好的响应关系.具体分析了叶绿素荧光峰绝对高度、基线高度、归一化高度(分别归一化到560nm附近最大反射率波段与近红外810nm附近最大反射率波段)及荧光峰积分面积(包括积分总面积、基线以下面积与基线以上面积)等儿种光谱特征与悬浮物浓度之间的关系,其相关系数(R2)分别为0.8822、0.7483、0.8901、0.8547、0.8927、0.8877、0.8632,平均相对误差分别为27.25%、41.03%、27.11%、25.75%、24.91%、25.47%、27.54%.总体反演精度较高,其中总积分面积法效果最好,基线高度法效果最差,而叶绿索荧光峰波段的位移与悬浮物浓度之间不存在明显的相关性.研究结果表明叶绿素荧光峰特征在浑浊内陆水体悬浮物浓度信息提取中具有很好的应用前景,该方法可为浑浊的二类水体悬浮物遥感反演提供了一个新思路.     

草源型可溶性有机物降解过程中活性氧物种产生过程

活性氧物种(ROS)参与天然水体系统中的光化学反应、氧化还原反应,是影响水体中有机污染物的迁移、转化、环境归宿及生态效应的重要因素.然而目前对草源型可溶性有机物(DOM)分解过程中ROS的产生过程并不清楚.本文通过室内模拟实验首先构建了室内测定3种ROS(~3CDOM~*、~1O_2、·OH)的方法,进而分析草源植物——苔草(Carex tristachya)残体浸出液中DOM光降解过程中ROS的产生过程.结果表明:ROS累积含量的产生随着DOM的降解逐渐升高在3种自由基含量中,~3CDOM*的产生含量最多,·OH产生含量低于另外2种ROS两个数量级.CDOM含量与~3CDOM~*、~1O2、·OH浓度呈现正相关关系,尤其与~3CDOM~*和~1O_2浓度的显著性水平最高,·OH次之.ROS浓度与水质指标呈现出不同的线性相关关系,与硝态氮浓度呈负相关关系,而与亚硝态氮浓度呈现正相关关系,并且亚硝态氮对ROS浓度影响效果极显著.同时类蛋白荧光峰值强度的衰减与ROS累积含量呈现极显著负相关关系,脱明在DOM的光降解过程中蛋白质小分子的降解是产生ROS很重要的一个部分.综上通过对草源型DOM光降解过程中ROS产生过程的研究,增加了对湖泊生态系统中水生植物产生ROS的过程、迁移、转化、归宿及其作用机制的认识.     

Organic carbon fluxes of a glacier surface: A case study of Foxfonna,a small Arctic glacier

Arctic glaciers are rapidly responding to global warming by releasing organic carbon (OC) to downstream ecosystems. The glacier surface is arguably the most biologically active and biodiverse glacial habitat and therefore the site of important OC transformation and storage, although rates and magnitudes are poorly constrained. In this paper, we present measurements of OC fluxes associated with atmospheric deposition, ice melt, biological growth, fluvial transport and storage (in superimposed ice and cryoconite debris) for a supraglacial catchment on Foxfonna glacier, Svalbard (Norway), across two consecutive years. We found that in general atmospheric OC input (averaging 0.63 ± 0.25 Mg a^-1 total organic carbon, i.e. TOC, and 0.40 ± 0.22 Mg a^-1 dissolved organic carbon, i.e. DOC) exceeded fluvial OC export (0.46 ± 0.04 Mg a^-1 TOC and 0.36 ± 0.03 Mg a^-1 DOC). Early in the summer, OC was mobilised in snowmelt but its release was delayed by temporary storage in superimposed ice on the glacier surface. This delayed the export of 28.5% of the TOC in runoff. Biological production in cryoconite deposits was a negligible potential source of OC to runoff, while englacial ice melt was far more important on account of the glacier's negative ice mass balance (–0.89 and –0.42 m a^-1 in 2011 and 2012, respectively). However, construction of a detailed OC budget using these fluxes shows an excess of inputs over outputs, resulting in a net retention of OC on the glacier surface at a rate that would require c. 3 years to account for the OC stored as cryoconite debris. © 2018 John Wiley & Sons, Ltd.     

Depositional environments and maturity evaluated by biomarker analyses of sediments deposited across the Cenomanian–Turonian boundary in the Yezo Group,Tomamae area,Hokkaido, Japan

Biomarker analyses for evaluating maturity of organic matter and depositional environments such as redox conditions, were performed in sediments across the Cenomanian–Turonian boundary (CTB) in the Saku Formation of the Yezo Group distributed along the Shumarinai‐gawa River and the Omagari‐zawa River, both in the Tomamae area, Hokkaido, Japan. Maturity indicators using steranes and hopanes, show that organic matter in sediments from the Shumarinai‐gawa and Omagari‐zawa sections are of lower maturity than those from the Hakkin‐gawa section (Oyubari area). Moreover, the ββ hopane ratios clearly show that the maturity of the Shumarinai‐gawa samples is lower than that of the Omagari‐zawa samples. These variations in the maturity of organic matter presumably reflect the difference in their burial histories. The results for the pristane/phytane (Pr/Ph) ratios suggest that the Shumarinai‐gawa samples were deposited under dysoxic to anoxic environments across the CTB, while the depositional environments of the Omagari‐zawa samples were relatively oxic. By another paleoredox indicator using C₃₅ homohopanoids including a homohopene index (HHenI), higher values are observed in the Shumarinai‐gawa section, particularly in the horizons of the preceding period and an early stage of the first negative shift phase and the latest oceanic anoxic event 2 (OAE2) interval. These results suggest that the Shumarinai‐gawa samples record dysoxic to anoxic environments across the CTB. In contrast, the signals for the C₃₅ homohopanoid index values show a relatively oxic condition in the Omagari‐zawa section. The trends of stratigraphic variations in redox conditions are different from those in the OAE2 interval in the proto‐Atlantic and Tethys regions as reported previously. Hence, the redox variations in the Tomamae area were basically related to a local environmental setting rather than global anoxia. However, the prominent anoxic emphasis observed in the HHenI profile of the Shumarinai‐gawa section can be a distinctive, and possibly global, event in the North‐West Pacific just before the OAE2.