内河DOM降解的三维荧光、紫外光谱研究——以白马河为例

利用三维荧光光谱、紫外光谱手段,研究白马河水样中DOM在微生物作用下的分解情况,经过微生物分解204 h后DOC的浓度下降为23%.根据双指数方程拟合,水样中易分解组分占总量的63.2%,易分解组分与难分解组分的分解常数分别为0.102 h-1,0.002 57 h-1.随着培养时间的延长,水样三维荧光光谱中单位浓度有机物的荧光强度有不同程度的提高.根据水样的紫外吸收光谱分析,培养过程中SUVA254 nm有逐步升高的趋势,而溶液250 nm与365nm吸收的比值没有明显变化.     

内河DOM降解的三维荧光、紫外光谱研究——以白马河为例

利用三维荧光光谱、紫外光谱手段,研究白马河水样中DOM在微生物作用下的分解情况,经过微生物分解204 h后DOC的浓度下降为23%.根据双指数方程拟合,水样中易分解组分占总量的63.2%,易分解组分与难分解组分的分解常数分别为0.102 h-1,0.002 57 h-1.随着培养时间的延长,水样三维荧光光谱中单位浓度有机物的荧光强度有不同程度的提高.根据水样的紫外吸收光谱分析,培养过程中SUVA254 nm有逐步升高的趋势,而溶液250 nm与365 nm吸收的比值没有明显变化.     

2011夏季南极普里兹湾营养盐与浮游植物生物量的分布

利用2011南极夏季在普里兹湾获取的海水样,检测了Chla、磷酸盐、硅酸盐、硝酸盐和铵盐的含量。结果表明,普里兹湾表层海水中Chla的含量普遍具有冰架边缘>陆架区>陆坡及深海区的分布特征,海冰的消融及水体的稳定性是影响表层海水Chla分布的主要原因。Chla含量的垂直分布与光照条件相关,具有上层水体含量高,随着深度逐渐降低的分布特征。磷酸盐、硅酸盐和硝酸盐的水平及垂直分布特征都与Chla的分布格局相反。表层海水中铵盐的分布特征与磷酸盐等主要营养盐的分布格局相反,冰架边缘、陆架区铵盐的垂直分布特征与陆坡及深海区不同,在冰架边缘和陆架区有机质降解过程主导着水柱中铵盐的浓度,而浮游植物吸收作用与有机质降解过程之间的平衡控制着陆坡及深海区铵盐的垂直分布。根据Chla与营养盐的浓度及分布特征,结合温度、盐度、溶解氧等水文要素,分析探讨了Chla深层最大值现象（DCM）的成因及67.5°S以南表层海水中铵盐对硝酸盐吸收的抑制作用。     

白洋淀沉积物间隙水中的自然有机质结构特征

利用紫外—可见吸收光谱(UV-Vis)研究白洋淀沉积物间隙水中的自然有机质(NOM)的结构和来源,通过提取自然有机质的UV-Vis图谱特征参数(HIX)发现,与入河口区和水产养殖区的采样点相比,淀区出水口区域采样点的沉积物间隙水中的自然有机质腐殖化程度较高,这表明淀区出水口区域沉积物间隙水中的自然有机质具有较高的芳香碳的结构。白洋淀沉积物间隙水中的自然有机质分层分析结果显示,表层沉积物(0~3 cm深)间隙水中的自然有机质腐殖化程度较低。特征参数E2/E3(UV-Vis在波长250 nm和365 nm处吸收率的比值)显示,白洋淀自然保护区采样点沉积物间隙水中的自然有机质主要来自胡敏酸源,河口区和养殖区采样点沉积物间隙水中的自然有机质主要来自生物源,其他采样点沉积物间隙水中的自然有机质则同时受到陆源和生物源的影响。     

南极普里兹湾表层海水中铜、镉、锌的分布

利用中国第24次南极考察获得的水样,研究了普里兹湾表层海水中痕量元素铜、镉、锌的含量及其分布。原子吸收分光光度法(AAS)测得普里兹湾铜、镉、锌的浓度范围分别为0·36-2.86、0.020-0.594、2.9-20.0μg·dm-3,平均值分别为1.15、0.143、11.2μg·dm-3。发现普里兹湾表层海水中铜、镉、锌的含量与南印度洋、南极海洋气溶胶及LarsemannHills湖泊群水体中的含量近似。研究表明,表层海水中铜、镉的含量及分布受悬浮颗粒物、初级生产力及盐度等的影响,锌可能受到了一定程度的人类活动的影响。     

广州市饮用水中消毒副产物卤乙酸的毒性及其降解研究

以2012年4月初与5月初所采集的广州市自来水管网水样为样本,通过实验手段分析广州市市政供水中的水源、管网水等供水水质情况,对饮用水中卤乙酸浓度进行监测,结果表明饮用水中总卤乙酸范围在5.91~45.75μg·L~(-1),符合美国EPA环保署对总卤乙酸含量的控制标准,其中二氯乙酸浓度范围为0.88~16.69μg·L~(-1),三氯乙酸浓度范围为3.72~27.00μg·L~(-1),均符合《生活饮用水卫生标准》(GB5749—2006)对其含量的限制。对二氯乙酸、三氯乙酸、一溴乙酸、二溴乙酸进行毒性检测中,测出这4种物质的细菌半致死效应浓度分别为184.07μg·L~(-1)、193.57μg·L~(-1)、13.47 mg·L~(-1)、15.00 mg·L~(-1)。以二氯乙酸、三氯乙酸为代表物质,用Fenton试剂氧化法降解模拟水样,利用气相色谱法测定降解后的卤乙酸浓度,考察了Fenton试剂用量、p H值、模拟水样初始浓度和反应时间对卤乙酸降解效果的影响。结果表明,100μg·L~(-1)的100 m L二氯乙酸、三氯乙酸模拟水样中投加0.4 mmol·L~(-1)H2O2溶液及0.04 mmol·L~(-1)Fe2+溶液,反应时间为20 min,初始pH值为3.6,为Fenton试剂氧化法降解二氯乙酸、三氯乙酸的最佳条件,降解率分别为69.28%和71.4%。     

洪泽湖不同湖区表层沉积物对磷的吸附特征

研究了洪泽湖9 个湖区表层沉积物对磷的吸附行为和沉积物对磷的吸附/解吸平衡质量浓度, 并分析了沉积物理化性质与磷吸附特征参数的关系。结果表明, 在低磷浓度条件下(0~1 mg/L), 沉积物对磷的最大吸附量为50.67~85.17 mg/kg, 沉积物在磷酸盐初始质量浓度较低时都存在负吸附(释放)现象。各湖区沉积物的吸附/解吸平衡磷浓度(EPC0) 范围为0.06~0.11mg/L, 均小于其上覆水中磷的含量, 沉积物对其上覆水中的磷表现为吸附作用。沉积物最大磷吸附量(Q_max)、本底吸附态磷量(NAP) 和总最大吸附磷量(TQ_max) 与沉积物中活性铁和活性铝的含量显著正相关, 与沉积物中总磷、无机磷、有机磷和有机质的含量相关性不显著。吸附/解吸平衡浓度(EPC₀) 与沉积物各理化参数之间没有表现出显著相关性。     

中国边缘海沉积物中239+240Pu的来源与存量模型

对海水和沉积物中^239+240Pu活度、²⁴⁰Pu/²³⁹Pu比值和^239+240Pu存量的分析,可以为海洋环境中水团输运、黑潮海水入侵、颗粒物通量、颗粒清除过程、污染物堆积、沉积年代等问题的研究提供有效途径。针对中国边缘海沉积物中^239+240Pu活度分布、²⁴⁰Pu/²³⁹Pu比值特征和^239+240Pu存量进行比较讨论,发现虽然全球大气沉降和太平洋核试验场的输入是中国边缘海沉积物中^239+240Pu的2个主要来源,但是中国边缘海海洋环境中不同区域Pu的来源的比例有差异。同时,文中系统探讨了利用Pu端元法研究中国边缘海海洋沉积物中^239+240Pu存量的质量平衡模型,这对认识海洋中沉积物的源与汇以及海洋放射性环境状况具有一定意义。     

基于近红外光谱快速分析东南极湖泊沉积物化学元素含量

以东南极罗斯岛地区的3个湖泊沉积剖面为研究对象,利用紫外-可见-近红外反射光谱仪获得了沉积物样品的光谱曲线,讨论了东南极罗斯岛湖泊沉积物的光谱特征。在沉积物化学元素分析的基础上将样品分成建模集和验证集,采用偏最小二乘法建立光谱与化学元素指标的对应关系矩阵,通过验证集预测值和测定值之间的误差参数比较,发现研究的20种元素含量均能和光谱曲线建立有效的计算关系,其中,N、C、H、Mn、Ba、P、Al、Fe、K、Se、As和Hg等元素能够达到相当精确的预测水平(预测值与测量值之间的相关系数r20.90)。本研究结果表明,利用近红外反射光谱快速分析东南极湖泊沉积物中元素含量是一种潜在有效的方法。     

西南极海沉积物碘的迁移与富集

本文研究了西南极不同地理环境沉积碘的地球化学迁移和富集机制 ,结果表明海湾和深海表层沉积物碘主要与有机质结合 ,但在陆架和半深海 ,与氧化物结合和吸附态碘可占相当大的比例。碘在表层沉积物中迁移的环境特征与铁类似 ,即在还原环境中迁移 ,在氧化环境中转入固相 ,然而碘在沉积物中主要并不是作为电子接受者 ,而是随有机质分解或氧化物还原后被释放进入液相。沉积物表层 I/Corg值高于浮游生物是由于吸附和氧化过程的参与。沉积物 I/Corg值随深度的降低代表了有机质分解 ,氧化物还原 ,粘粒物质解析及间隙水碘扩散的综合效应。沉积物碘的扩散通量与沉积通量在同一数量级水平解释了沉积岩贫碘的原因。根据计算和讨论结果重新提出了海洋沉积物碘迁移和富集的地球化学模式。     

东南极拉斯曼丘陵湖泊沉积生物标志物记录及其环境气候意义

东南极拉斯曼丘陵地区莫愁湖（69°22.3’ S,76°22.0’ E）沉积柱中的有机生物标志物记录了全新世中晚期该地区气候演变过程。不饱和长链烯酮在沉积柱111-76 cm （6450-5100 cal. yr. BP）和36-30 cm（3700-3500 cal. yr. BP）深度有检出,76 cm深度以上基本消失,表明该地区在5100 cal. yr. BP前后气候开始由冷转暖,冰川消融,陆壳抬升,相对海平面下降,同时大量的冰融水使湖泊逐渐淡化。沉积柱底部长链烯酮的检出阶段与东南极相对海平面较高时期相一致,而沉积柱36-30 cm（3700-3500 cal. yr. BP）深度不饱和长链烯酮的痕量检出则揭示了一个短暂的气候干冷,湖泊盐度升高的时期。沉积物中正构烷烃反映的当地气候变化所控制的湖生植物群落演变过程与上述过程基本一致。     

西藏山南地区沉错湖泊与径流水化学特征及主控因素初探

选取枪勇冰川径流-卡鲁雄曲（河）-沉错（湖）为研究区域,开展高原湖泊及其补给河流与冰川径流的水化学特征研究,并探讨影响主离子组成的主控因素。结果表明：夏季湖水主要离子呈均匀混合状态,pH值、电导率、TDS及优势阴阳离子在整个湖泊空间上变化不显著;总体上,从上游冰川融水径流、河水至下游湖泊,离子浓度呈现上升趋势;融水径流及河水的水化学类型主要受岩石风化作用控制,表现为SO₄^2--Ca²⁺-Mg²⁺类型;沉错湖水的水化学类型主要受蒸发结晶作用控制,表现为SO₄^2--Na⁺-Ca²⁺类型,在蒸发作用下Ca²⁺逐渐沉淀析出,Na⁺浓度不断升高而成为绝对优势阳离子。     

The lacustrine depression at Annecy (France), geological setting and Quaternary evolution

The Annecy lacustrine depression lies in a tectonic transverse valley of structural origin, linking the present day towns of Annecy and Ugine and bounded by the Bauges and Bornes massifs. Only the last two major glacial periods are represented in the stratigraphic and geomorphic evidence from the area, but its successive glaciations that have been largely responsible for the form of the valley within which the present day lake lies. Of particular importance were the lobes of the Arve glacier, one shaping the depression from the south-east; the other from the north. The retreat of the glaciers left behind a more extensive precursor of the present day Lac d'Annecy, which latter constitutes the residual body of open water after lake level lowering, partial infilling and drainage diversions within the catchment. The drainage basin of the extended lake formed shortly after the last glacial maximum (LGM) in the region. Its extent can be determined from field sampling and coring and its elevation can be established at 460 m above present day sea level. The present day lake is more isolated, since the Fier river, to the north, no longer drains into it. To the southeast, the course of the Chaise river has also been diverted, leaving the lake's drainage basin reduced to half its post-LGM size. The major paleogeographical events in the Late-Quaternary evolution of the basin are described in chronological sequence.     

环青海湖地下水溶解性碳的时空变化特征

区域地下水溶解性碳的时空变化特征研究对于认识区域物质循环和能量传递及推动区域生态可持续发展具有重要意义。本研究在青海湖流域冻结期和融化期分别收集了地下水、河水和湖水样品,研究了环青海湖地下水在冻结期和融化期的溶解性碳特征,并探究了不同类型地下水的溶解性碳特征及其对不同冻融时期的响应,最后揭示了环湖区域不同水体的溶解性碳的差异特征及影响因素。结果表明：冻结期地下水、河水和湖水的溶解性无机碳（DIC）均相对高于融化期,溶解性有机碳（DOC）均相对低于融化期。地下水、河水和湖水的溶解性碳均主要以DIC为主,DIC在溶解性碳的占比高达92%。地下水的DIC平均含量在基岩裂隙水、水量中等和浅埋藏的水文地质条件下相对较高,DOC平均含量在基岩裂隙水、水量丰富和浅埋藏的水文地质条件下相对较高。地下水的DIC在湖滨平原砂砾石层、淤泥质砂层潜水和水量中等的水文地质条件下受冻融期影响较大,DOC在基岩裂隙水和水量贫乏的水文地质条件下受冻融期影响较大。湖水的DIC和DOC均远高于河水和地下水。河水的DIC在融化期和冻结期均低于地下水,DOC在融化期高于地下水,在冻结期低于地下水。     

夏季西北冰洋表层淡水分布的总碱度示踪研究

利用中国第三次北极科学考察在西北冰洋所进行的海水总碱度的测量,通过海水、海冰融化水以及河源淡水三个端元总碱度特征的显著差异计算西北冰洋夏季表层海水中淡水所占的比例。研究表明,西北冰洋海冰融化水所占比例最大区域在加拿大海盆区75°N附近,这是冰缘带位置,往北向高纬度的冰密集中逐渐增加。而河源淡水的组份则与北冰洋的环流密切相关,并且在西北冰洋水体中逐渐累积。     

西藏纳木错东部湖水及入湖河流水化学特征初步研究

对西藏纳木错东部湖区中不同点位的湖水和周边不同位置的入湖河流进行取样,水化学分析结果表明:在主要阴阳离子组成中,Na+和Ca2+分别是湖水和河水的主要阳离子,分别占其阳离子总量的72.4%和71.9%.而湖水和河水的主要阴离子都是Hco3-,分别占其阴离子总量的71.9%和91.2%.从水化学的控制影响因素来看,纳木错湖水主要受蒸发-结晶作用控制,而河水则主要受岩石风化作用影响,其中碳酸盐和硅酸盐的风化影响最为重要,其次是部分蒸发岩的溶解,而区域内湖水蒸发与大气海盐传输也有一定的贡献.     

近50 a博斯腾湖逐年水量收支估算与水平衡分析

据博斯腾湖流域1958-2010年期间主要河流开都河、黄水沟、清水河、孔雀河的逐年流量资料,结合焉耆盆地降水、蒸发要素的同期观测资料,对大湖区的逐年水量收支进行计算,并依据水量平衡原理对博湖大湖区残差水量进行了逐年分析。结果表明：（1）1958-2010年期间年均入湖水量14.34×10⁸ m³/a,其中入湖河水约占95%;年均输出水量13.96×10⁸ m³/a,其中大湖区输入孔雀河水量约占43%,湖面蒸发耗水量占57%;湖区年均蓄水量71.57±3.92×10⁸ m³10⁸ m³/a,湖水年均水位为1 047.01±0.94 m;（2）极端水文年度水量平衡分析指出：1986年为最枯年份,入湖河水是多年平均值的62%,而出湖河水量是多年平均值的153%,导致年内湖区水位下降0.94 m;2002年最丰年份入湖河水是多年平均值的2.6倍,致使年内水位上升0.80 m;（3）残差水量逐年“正负”变化指出,湖水与地下水之间存在互补关系,过去53 a间湖水补给地下水的年均水量为0.87×10⁸ m³/a。     

RIVER SYSTEM AND DISTURBANCE FACTORS IN THE LAKE TOBA

Situated at an elevation of 905 m above sea level in the Province of North Sumatra, Lake Toba and its surrounding landscapes are regarded as a natural heritage in a certain extent, as a quoted national treasure. Unfortunately degradation of the land and water resources in the watershed along Lake Toba is taking place at an alarming and totally unacceptable rate. The quality of the lake is partly depended on input the quality of the rivers. When compared to the control area the water quality that influenced by the piggeries are highly polluted. It can be concluded that the Salbe River at the downstream of the piggeries has been polluted and apparently it is a serious problem to the catchment area management. It should be noted that the polluted river would influence the water quality of the Lake Toba. Based on calculation, the permissible BOD5 according to B- river standard is 238 mg/L, it means the river still in B standard but the condition and quality are decreasing continuously. Following the Indonesian health standard the permissible BOD is - 461 mg/L. It means BOD in the river should be reduced 461 mg/L or clean program is needed.     

Sediment supply and climate change: implications for basin stratigraphy

The rate of sediment supply from erosional catchment to depositional basin depends primarily upon climate, relief, catchment slope and lithology. It varies in both time and space. Spatial changes in erosion rates due to variations in lithology are illustrated by contrasting rates of drainage divide migration away from faults of known ages. Time variations in relative sediment supply are extremely complex and vary widely according to the direction and magnitude of climate change. In many parts of the Great Basin and south-western USA, glacial maximum climates were characterized by higher effective moisture and the altitudinal downward spread of woods and forests. Sparse data from alluvial fans indicate reduced sediment supply, despite the increased runoff evident from higher lake levels. The situation in Mediterranean areas is less clear, with rival climatic scenarios for vegetation ecotypes predicting contrasting runoff. In order to test these latter we run Cumulative Seasonal Erosion Potential [CSEP] experiments for present-day and a variety of full-glacial Mediterranean candidate climates. The results indicate the likelihood of enhanced sediment supply and runoff compared to the present day during full-glacial times for a cool wet winter climate and a reduction in sediment supply and runoff for a full-glacial cool dry winter climate. We then explore the consequences of such phase differences in sediment supply, and sea and lake levels for the stratigraphy of sedimentary basins. Highstands and lowstands of sea or lake may be accompanied by greater or lesser sediment and water supply, as determined by the regional climate and the direction of climatic change. Thus marine lowstands are not necessarily periods of great transfer of coarse clastic sediments to shelves and deep water basinal environments. Unsteady sediment supply has greatest implications for alluvial systems, in particular the effect that changing relative supplies of water and sediment have upon river and fan channel incision.     

Composition, spatial distribution, and environmental significance of water ions in Pumayum Co catchment, southern Tibet

The chemistry of major cations (Mg2+, Ca2+, Na+, and K+) and anions (HCO3 ?, SO4 2?, and Cl?) in the water of Lake Pumayum Co and its inflow river was studied, revealing the obvious ionic difference among various inflow rivers and the lake. The chemical type of the lake water was Mg2+-Ca2+-HCO3 ?-SO4 2+, but the major ions of the main inflow rivers were Ca2+-Mg2+-HCO3 ?. In the lake inlet of Jiaqu River, the main inflow river, there was significant variance of water chemistry within the depth less than 2 m. However, it was almost homogeneous at other area of the lake. Therefore, with the evidence of distribution of water chemistry and oxygen isotope of lake water, a conclusion can be outlined that Jiaqu River had a distinct effect on the hydrochemistry of the water on the submerged delta, whereas this is not the case for other rivers. The Gibbs plot revealed that the dominant mechanism responsible for controlling chemical compositions of the lake water was rocks weathering in the drainage area. Ion ratios and ternary plots further explored the main processes controlling the water chemistry of the catchment, i.e., carbonate weathering, pyrite weathering, and silicate weathering. The different hydrochemistry characteristics between river water and lake water may result from the CaCO3 precipitation. The findings will benefit the explanation of the environmental significance of carbonate in paleolimnological studies in the lake.