前处理方法对北黄海沉积物粒度的影响

采用不同方法对北黄海底质样品进行了粒度分析前处理，以探讨有机质和碳酸盐对北黄海沉积物粒度的影响。结果表明，去除有机质或碳酸盐后，粗粒沉积物（呈双峰分布）粒度分布的峰态明显变宽，平均粒和戏及粗颗粒（＞32μm）组分含量明显增加；而细粒沉积物的粒度分布发生明显细偏，表现为众数的细化及平均粒径和粗颗粒含量的降低。北黄海底质沉积物的有机碳含量变化与沉积物的平均粒径呈明显的负相关，暗示了浅海沉积物中有机碳的输运和积聚主要是伴随着细颗粒组分发生；而碳酸盐含量同沉积物粒度的关系不甚明确，可能与沉积物物源的关系更为密切。     

酸化过程对海洋沉积物中有机碳同位素分析的影响

海洋沉积物中有机碳同位素(δ13C)可以示踪海洋生态系统中有机质来源,对环境研究具有重要意义。分析沉积物中有机物的δ13C,需要对样品进行酸化,以去除无机碳的影响。由于不同来源的沉积物中无机碳的含量和组份存在差异,需要针对样品性质,优化酸化处理过程。本研究分别选取了无机碳含量不同的温带与热带河口、海湾沉积物样品,比较了3种不同酸化过程对有机物δ13C分析的影响。研究结果表明:方法1(酸洗法)中6%H_2SO_3和1mol/L H_3PO_4对无机碳含量较高的热带河口、海湾样品去除效率较低,而2mol/L HCl去除无机碳酸盐的效果较理想。方法2(酸蒸法)并不适用于无机碳含量较高的热带河口、海湾样品;而对于无机碳含量相对较低的温带河口、海湾样品,9h酸蒸较为适宜。方法3(非原位酸洗)的结果较方法1和方法2偏正,表明其对含13C丰富的有机组分破坏较小,且方法3中残留的酸对δ13C的分析没有影响。因此,方法3是去除海洋沉积物中无机碳较理想的方法。     

渤海及北黄海河流悬浮颗粒碳氮同位素时空分布及源解析

选择流入渤海和北黄海的36条主要河流为研究对象,对比了平水期、丰水期和枯水期水体中悬浮颗粒物和河流表层沉积物的碳和氮稳定同位素的地球化学特征,并对颗粒物有机质碳和氮来源进行分析。结果表明,水体悬浮有机质碳同位素总体上表现为δ13C平水期δ13C丰水期δ13C枯水期的特点,δ15N值呈δ15N丰水期δ15N平水期δ15N枯水期的特点。渤海和北黄海的主要入海河流悬浮颗粒物有机质的来源具有明显的季节性差异,悬浮颗粒有机质碳平水期(春秋季)来源以C3植物、土壤有机质和水生藻类为主,丰水期(夏季)碳的各来源中浮游植物的贡献率明显增大,枯水期(冬季)则表现为陆源C3植物分解和水源性有机质的混合来源;悬浮颗粒态氮的来源与季节性降水量、生活污水、合成化肥及河流内源性水生植物密切相关。     

鸭绿江河口西岸潮滩沉积物有机质对流域变化的响应

河流颗粒有机质提供了陆地碳循环的重要信息以及人类活动的记录,通过河口地区沉积物有机质组成,可反映流域变化及海陆间相互作用。2010-2011年分两次于鸭绿江河口西岸潮滩采集柱样4根及表层样23个。对样品进行有机质碳氮总量(TOC、TN)、碳氮同位素(δ13C、δ15 N)及沉积物粒度测试。分析结果表明,由河口向西,有机质受改造程度加深且来源逐渐复杂化,致TOC/TN与δ13C的相关性逐渐降低,δ15 N与沉积物粒度的相关性也随之降低。文中以δ13C为主线探讨沉积物有机质的来源及运移,TOC/TN作为辅助,δ15 N则用于指示生化条件的改变。柱样的δ13 C分布与河流入海输沙密切相关,水库对入海泥沙的拦截,致河口潮滩沉积速率减缓,从而增加了沉积物中海源有机质的含量,δ13C随之增加。潮滩西侧柱样的δ15 N增加指示了生活工业污水的大量排放。此外,表层样δ13C分布的方向性,指示了西水道门口处的快速堆积及潮下带物质的向岸运移,并在西岸潮滩向岸一侧富集。     

不同预处理方法对南海东沙海域沉积物粒度的影响

通过采用不同方法对东沙沉积物样品进行了预处理,并采用综合法进行了粒度分析,以探讨东沙沉积物中碳酸盐和有机质对其粒度的影响。结果表明,去除有机质后沉积物的平均粒径和63～4μm粒径范围内的组分明显减小,有机质含量变化与平均粒径变化呈明显负相关,说明东沙沉积物中有机质的沉积是伴随细粒悬浮物质和胶体物质沉积下来的,且对细颗粒有明显的絮凝作用;去除碳酸盐后沉积物的平均粒径呈减小趋势,但粒径范围内组分含量的变化不明显,且碳酸盐含量的变化与沉积物粒径变化的关系也不甚密切。     

青海湖沉积物有机碳含量与同位素和粒度特征及其古气候意义

对青海湖沉积物中粒度参数、总有机碳（TOC）含量及其δ^13C值的形成条件与环境气候的关系进行了研究。结果表明：在暖湿时期，沉积物中有机碳含量（TOC）较高，有机质的δ^13C值较高，沉积物的平均粒径较细；反之，在冷干时期，沉积物中有机碳含量（TOC）较低，有机质的δ^13C值较低，沉积物的平均粒径较粗。反映出沉积物中TOC含量、有机质δ^13C值及粒度特征与气温具有良好的相关性。结合^14C测年，分析了湖区古气候演化序列，表明自8500aBP以来湖区气候经历了4个演化阶段：即暖湿－凉干－温湿－冷干的变化过程。     

胶州湾潮间带沉积物有机碳和叶绿素的埋藏特征

于2004年9月,在胶州湾潮间带河套和红石崖两个区域(分别代表近河和近海区域)分别采集沉积物柱状样品,并分析了样品中有机碳和叶绿素含量。结果表明:(1)胶州湾潮间带沉积物有机碳和总氮质量比分别为1.0～3.0g/kg和0.1～0.3g/kg,随沉积物埋藏深度表现为波动变化,但无明显规律性;(2)胶州湾潮间带沉积物从表层到底层叶绿素a质量比的总体趋势是逐渐降低最后趋于稳定,叶绿素a质量比变化为0.3～5.2g/kg;(3)胶州湾潮间带沉积物中的有机质应属于混源有机质。本实验结果对探讨胶州湾潮间带近河和近海区域沉积物中有机碳和叶绿素的埋藏和降解规律有重要意义。     

环渤海地区河流河口及海洋表层沉积物有机质特征和来源

2013年8月采集了环渤海地区35条主要河流河口表层沉积物样品,12月采集了渤海与北黄海24个表层沉积物样品,分析了其生物地球化学指标:总有机碳(TOC)、总氮(TN)、有机碳同位素(δ13C)和氮同位素(δ15N),探讨该区域表层沉积物有机质特征及组成。研究表明:河流河口表层沉积物有机碳同位素(δ13C)值在–26.4‰—–21.8‰,平均值为–24.5‰;渤海表层沉积物有机碳同位素(δ13C)值在–23.8‰—–21.7‰,平均值为–22.3‰。河口表层沉积物TOC含量在0.06%—3.87%,平均值为1.31%;渤海表层沉积物TOC含量在0.52%—2.09%,平均值为1.08%。河流δ13C富集较轻,偏向陆源;海洋δ13C富集较重,偏向水生有机质来源。河流河口表层沉积物的δ13C值差异较明显,最大值与最小值相差4.6‰,但是流域地理位置距离近的河流δ13C值差异不大。河流河口表层沉积物δ15N在1.5‰—10.2‰,平均值为5.5‰;渤海表层沉积物δ15N在4.4‰—5.6‰,平均值为5.0‰。河流表层沉积物δ15N范围比渤海表层沉积物δ15N范围广,原因是河流受陆源有机物影响,且陆源有机物来源差异大。海洋表层沉积物δ15N相对均一,说明海洋表层沉积物δ15N受物源影响较小,体现了水体中有机质的转化和微生物活动对氮同位素的影响。本研究中表层沉积物的δ13C与δ15N没有明显的相关性,也体现了陆源有机质输入的影响。根据经典的二元模式计算,35条河流陆源有机质的贡献比例范围为10%—90%,平均值为60%;渤海陆源贡献比例范围为10%—50%,平均值为20%。河流有机质的来源以陆源有机质为主,水生有机质为辅。渤海有机质的来源以水生有机质为主,环渤海河流的陆源输入也有重要贡献。需要指出的是,有机碳同位素(δ13C)、氮同位素(δ15N)和Corg/Ntotal对有机质来源判别有一定局限性,虽然稳定同位素有示踪性,然而其成分仍然不可避免地受到生物地球化学等过程的改造,在使用稳定同位素技术示踪物源时,须小心谨慎。     

Logatchev热液场附近表层沉积物中有机质的组成特征、来源及其影响因素

利用2005年"大洋一号"科学考察船电视抓斗采样器采集的表层沉积物样品,对大西洋洋中脊Logatchev热液场附近7个站位表层沉积物样品中的烷烃组分进行了定量分析,并结合总有机碳(TOC)及C稳定同位素(δ13C值)分析,探讨了表层沉积物中有机质的组成及可能的来源和影响因素.结果表明:表层沉积物中正构烷烃组分以低碳数化...     

珠江口外近海沉积有机质化学及稳定同位素组成的早期成岩改变

理解早期成岩过程中有机质的化学和同位素分馏对于研究海洋和湖泊环境中的生物地球化学过程是很重要的。将珠江口外近海生物成因有机质分为可水解氨基酸、碳水化合物、脂类和酸不溶四个部分,分析了有机质的化学和同位素组成(δ13C,δ15N),借以讨论沉积有机质在埋藏的早期成岩过程中所发生的化学和同位素改变,结果表明,从浮游生物→悬浮颗粒物→表层沉积物→沉积柱内部,易降解组分可水解氨基酸、碳水化合物、脂类占样品总有机碳的份额依次降低。沉积物及四个有机部分的稳定碳同位素组成在纵向上随深度保持相对恒定,而在不同有机部分之间差异明显。不同类型有机物的分解速率差异在改变有机质化学成分的同时,导致其δ13C发生小幅度负向漂移;细菌有机质的形成和分解对有机质化学成分和同位素组成演化也有重要贡献,并且在一定程度上抵消了上述δ13C的负向漂移,其结果导致沉积有机质的δ13C略低于浮游生物;另一方面,由于异养菌生长过程中的氮同位素分馏系数与可利用氮源的特征和培养基的性质等多种因素有关,导致沉积物的δ15N变化范围增大。在这里δ13C可以可靠地指示该海域沉积有机质的来源,而δ15N变化范围较大且规律不明显,难以用作沉积有机质来源的指示。     

中国鱼类名录Ⅻ--鳚亚目、(鱼衔)亚目、喉盘鱼亚目、鰕虎鱼亚目、微体鱼亚目、刺尾鱼亚目、带鱼亚目、鲭亚目、鲳亚目、金枪鱼亚目、攀鲈亚目、刺鳅亚目

鳚亚目 4 科 33 属 95 种，鰕虎鱼亚目 5 科 98 属 259 种，刺尾鱼亚目 5 科 11 属 65 种，鲈形目 19亚目 104 科 535 属 1799 种。     

The distribution of Mn,Fe, Cu,Ni, Co,Ga, Cr,V, Ba,Sr, Sn,Zn, and Pb,in some soil-sized particulates from the lower troposphere over the world ocean

Soil-sized particulates have been collected on board ship by a mesh technique from the lower troposphere of the North, Equatorial and South Atlantic Ocean, northern and southern Indian Ocean, South and East China Sea and various coastal localities.Spectrographic analysis reveals that, on average, the particulates have concentrations of Mn, Ni, Co, Ga, Cr, V, Ba, and Sr which are of the same order of magnitude as those in average crustal material. In contrast, the average concentrations of Pb, Sn, and Zn are one order of magnitude higher than those in average crustal material.Within this “world-wide” average there are significant geographical variations in the distributions of Pb, Sn, and Zn which may be related to anthropogenic sources.On the basis of trace-element distributions lower tropospheric soil-sized marine particulates have been divided into four genetic components; local, zonal, inter-zonal, and global. The proportions of these components vary geographically, and each component may have both a natural and an anthropogenic fraction.     

Distribution, abundance, and growth of larval tautog, Tautoga onitis, in Buzzards Bay, Massachusetts, USA

Tautog, Tautoga onitis, is an abundant species of fish in estuaries of the northeastern United States. Planktonic tautog larvae are abundant in summer in these estuaries, but there is little information on rates of growth of tautog larvae feeding on natural assemblages of food in the plankton. We examined abundance and growth of larval tautog and environmental factors during weekly sampling at three sites along a nearshore‐to‐offshore transect in Buzzards Bay, Massachusetts, USA during summer 1994. This is the first study of a robust sample size (336 larvae) to estimate growth rates of field‐caught planktonic tautog larvae feeding on natural diets, using the otolith daily‐growth‐increment method. The study was over the entire summer period when tautog larvae were in the plankton. The sampling sites contrasted in several environmental variables including temperature, dissolved oxygen (DO), and chlorophyll a concentration. There was a temporal progression in the abundance of tautog larvae over the summer, in relation to location and temperature. Tautog larvae were first present nearshore, with a pronounced peak in abundance occurring at the nearshore sites during the last 2 weeks in June. Larvae were absent at this time further offshore. From late June through August, larval abundance progressively decreased nearshore, but increased offshore although never approaching the abundance levels observed at the nearshore sites. The distribution and abundance of tautog larvae appeared to be related to a nearshore‐to‐offshore seasonal warming trend and a nearshore decrease in DO. Otoliths from 336 larvae ranging from 2.3 to 7.7 mm standard length had otolith increment counts ranging from 0 to 19 increments. Growth of larval tautog was estimated at 0.23 mm·day^?1, and length of larvae prior to first increment formation was estimated at 2.8 mm indicating that first increment formation occurs 3–4 days after hatching at 2.2 mm. Despite spatial and temporal differences in environmental factors, there were no significant differences in growth rates at any of three given sites over time, or between sites. Because larval presence only occurred at a narrow range of temperature (17–23.5 °C) and DO (6.5–9.3 mg·l^?1), in situ differences in growth did not appear to be because of differences in larval distribution and abundance patterns relative to these parameters.     

Arsenic,barium, germanium,tin, dimethylsulfide and nutrient biogeochemistry in Charlotte Harbor,Florida, a phosphorus-enriched estuary

Concentrations of dissolved nutrients (NO₃, PO₄, Si), germanium species, arsenic species, tin, barium, dimethylsulfide and related parameters were measured along the salinity gradient in Charlotte Harbor. Phosphate enrichment from the phosphate industry on the Peace River promotes a productive diatom bloom near the river mouth where NO₃ and Si are completely consumed. Inorganic germanium is completely depleted in this bloom by uptake into biogenic opal. The $\text{Ge}\text{Si}$ ratio taken up by diatoms is about 0·7 × 10^?6, the same as that provided by the river flux, confirming that siliceous organisms incorporate germanium as an accidental trace replacement for silica. Monomethylgermanium and dimethylgermanium concentrations are undetectable in the Peace River, and increase linearly with increasing salinity to the seawater end of the bay, suggesting that these organogermanium species behave conservatively in estuaries, and are neither produced nor consumed during estuarine biogenic opal formation or dissolution. Inorganic arsenic displays slight removal in the bloom. Monomethylarsenic is produced both in the bloom and in mid-estuary, while dimethylarsenic is conservative in the bloom but produced in mid-estuary. The total production of methylarsenicals within the bay approximately balances the removal of inorganic arsenic, suggesting that most biological arsenic uptake in the estuary is biomethylated and released to the water column. Dimethylsulfide increases with increasing salinity in the estuary and shows evidence of removal, probably both by degassing and by microbial consumption. An input of DMS is observed in the central estuary. The behavior of total dissolvable tin shows no biological activity in the bloom or in mid-estuary, but does display a low-salinity input signal that parallels dissolved organic material, perhaps suggesting an association between tin and DOM. Barium displays dramatic input behavior at mid-salinities, probably due to slow release from clays deposited in the harbor after catastrophic phosphate slime spills into the Peace River.     

Large amplitude, leaky, island-generated, internal waves around Palau, Micronesia

Three years of temperature data along two transects extending to 90 m depth, at Palau, Micronesia, show twice-a-day thermocline vertical displacements of commonly 50–100 m, and on one occasion 270 m. The internal wave occurred at a number of frequencies. There were a number of spectral peaks at diurnal and semi-diurnal frequencies, as well as intermediate and sub-inertial frequencies, less so at the inertial frequency. At Palau the waves generally did not travel around the island because there was no coherence between internal waves on either side of the island. The internal waves at a site 30 km offshore were out-of-phase with those on the island slopes, suggesting that the waves were generated on the island slope and then radiated away. Palau Island was thus a source of internal wave energy for the surrounding ocean. A numerical model suggests that the tidal and low-frequency currents flowing around the island form internal waves with maximum wave amplitude on the island slope and that these waves radiate away from the island. The model also suggests that the headland at the southern tip of Palau prevents the internal waves to rotate around the island. The large temperature fluctuations (commonly daily fluctuations ≈10 °C, peaking at 20 °C) appear responsible for generating a thermal stress responsible for a biologically depauperate biological community on the island slopes at depths between 60 and 120 m depth.     

4-溴苯甲酸-2,3,4,5,6-五溴苯酯的合成(英文)

以苯酚和4—溴苯甲酸为原料,合成一种尚未见文献记载的新化合物——4—溴苯甲酸—2,3,4,5,6—五溴苯酯,用无水三氯化铝催化苯酚的全溴化。此产物可望在阻燃剂方面得到应用。