3种海洋硅藻不同培养阶段挥发性成分的比较分析

本文应用顶空固相微萃取气相色谱-质谱联用技术,对威氏海链藻Thalassiosira weissflogii、小新月菱形藻Nitzschia closterium、角毛藻Chaetoceros calcitrons 3种硅藻的挥发性成分进行分析。结果表明,在3种硅藻的培养过程中,其挥发性成分除了壬醛及醇类呈现先增后降的趋势外,大多数不饱和醛类的含量在不断增加,烷烯烃类物质在不断减少,而乙酸乙酯、2-甲基-2-丙酸甲酯这类酯类化合物在角毛藻衰败期会显著富集。通过对代表性饵料硅藻的挥发性成分进行研究,可为海水养殖过程中微藻投喂种类、投喂时机的选择提供理论依据,并为海洋硅藻的进一步开发奠定基础。     

壳寡糖对番茄叶挥发性抗真菌物质及植保素日齐素的诱导效应

研究了 0 .3 %壳寡糖诱导番茄 (Lycopersiconesculentum )叶 12 0h后 ,其挥发性物质对番茄枯萎病菌 (Fusariumoxysporum )孢子萌发和菌丝生长的影响 ;采用气相色谱 质谱联用技术 ,检测诱导后番茄叶挥发性物质及植保素日齐素质和量的变化。结果表明 :经壳寡糖诱导后 ,番茄叶挥发性物质对病菌的抑制率较对照组的提高。番茄叶挥发性抗真菌物质总含量为对照组的 1.49倍 ;氧合脂类、萜类及芳香类化合物的含量分别提高了 61% ,10 %和 69%。其中 (E) 2 乙烯醛含量增加了 64 % ,水杨酸甲酯含量增加了 3 8% ,壳寡糖不能诱导番茄植保素日齐素的合成。     

色谱／质谱（GC／MS）联用技术分析测定海藻中的石油烃和多环芳烃

本文介绍了ＧＣ－ＭＳ联用技术－特征离子选择法测定海藻中石油烃和多一并主烃的分析方法。     

三种扇贝挥发性风味物质指纹图谱分析

为探究海湾扇贝(Argopecten irradians)、栉孔扇贝(Chlamys farreri)、虾夷扇贝(Patinopecten yessoensis)三种扇贝闭壳肌的挥发性风味物质差异,采用气相色谱-离子迁移谱(gas chromatography-ion mobility spectroscopy,GC-IMS)技术,对三种扇贝闭壳肌在新鲜(40℃)和加热(100℃)情况下进行挥发性成分分析。结果表明:在新鲜状态下,海湾扇贝(HWSB-F)、栉孔扇贝(ZKSB-F)、虾夷扇贝(XYSB-F)闭壳肌中,共定性出27种挥发性风味物质,其中醛类8种,醇类5种,酮类5种,酯类3种,以及醚类、苯类、酸类、烯类和噻唑等。在加热情况下,海湾扇贝(HWSB-C)、栉孔扇贝(ZKSB-C)、虾夷扇贝(XYSB-C)闭壳肌中共定性出52种挥发性风味物质,其中醛类20种,酯类5种,酮类7种,醇类8种,烯类4种,酸类2种,醚类2种,还包括吡嗪、胺类、苯类、含氧杂环等物质。对三种扇贝闭壳肌新鲜组和加热组指纹图谱进行分析,发现新鲜扇贝原有的挥发性风味物质加热后减少,且产生了新的其他种类的挥发性风味物质。扇贝闭壳肌加热组的挥发性风味物质种类较多,组成比较复杂,新鲜组的扇贝闭壳肌挥发性风味物质种类较少,组成简单。通过主成分分析,可在新鲜状态和加热状态下,有效区分三种扇贝闭壳肌组织。三种扇贝闭壳肌挥发性风味物质指纹图谱的建立,丰富了不同扇贝呈味物质的组成成分研究内容,证明GC-IMS技术可快速鉴别三种去壳扇贝闭壳肌的种类,为不同种扇贝闭壳肌以次充好提供检测依据。     

海藻糖类的气相色谱分析 Ⅱ.红藻及红藻多糖中D-半乳糖和3, 6-内醚半乳糖的测定

红藻中的糖类主要以多糖形式存在(琼胶、卡拉胶等)，其中主要的单糖组分是D-半乳糖和3, 6-内醚半乳糖，除此之外还含有少晕的木糖、葡萄糖及甘露糖等成分。由于各单糖的相互干扰，难以用比色等着通化学分析方法对每一种单糖准确地定性定量。作者曾研究过褐藻中单糖的气相色谱测定法, 但该法不能测定3, 6-内醚半乳糖，囚为这种内醚糖对酸水解不稳定。据Dutton和Nozawa等人报道, 将多糖经甲醇分解后进行气相色谱分析，结果令人满意。本文用琼胶(Difco bacto-agar)作代表，研究探讨了红藻胶甲醇-HCI分解的条件，确定了红藻胶中D-半乳糖和3, 6-内醚半乳糖的气相色谱分析方法，并将其应用于红藻中D-半乳糖和3, 6-内醚半乳糖的分析。     

红树植物木榄叶中挥发油的化学成分

以正己烷为溶剂,采用回流提取法提取红树植物木榄叶中的挥发油,运用毛细管气相色谱-质谱联用技术分离检测得到40个峰,鉴定了其中的32种成分,被鉴定成分占挥发油总量的91.92%,其主要成分为烷烃类(30.31%)、萜类化合物(25.22%)、芳香化合物(14.07%)、酸(10.60%)、酯(5.36%)和烯(3.49%).     

PAEs类环境激素在草鱼（Ctenopharyngodonidellus）脏器中代谢研究

利用GC-FID建立了草鱼血清、肝胰脏、小肠及肝细胞培养液中邻苯二甲酸二乙酯（DEP）、邻苯二甲酸二丁酯（DBP）、邻苯二甲酸丁基苄酯（BBP）和邻苯二甲酸二乙基己基酯（DEHP）同时检测方法,并利用LC-MS／MS方法进行了DEP、DBP、BBP及DEHP在草鱼脏器中的代谢规律研究,以揭示邻苯二甲酸酯类（Phthal...     

紫菜特征挥发性物质分析

应用顶空固相微萃取和气相色谱-质谱联用技术,对坛紫菜(Porphyra haitanensis)、条斑紫菜(Porphyra yezoensis)与其一个突变品系的生长藻体挥发性物质进行分析,共分离鉴定出66种挥发性组分,3个紫菜试样中分别含有36、44和45种.鉴定组分中有21种为紫菜共有挥发性物质,其中8-十七烯和...     

海藻主要药用成分的研究和展望

对海藻主要药用成分的研究进行了综述。海藻内含有大量有益于人类健康的药用活性成分 ,其多糖、不饱和脂肪酸、蛋白质、氨基酸、多肽、牛磺酸、多萜、甾类和酶等成分具有抗凝血、降血压、降血脂、抗肿瘤等独特功能 ,可用于预防和治疗高脂血症、动脉硬化、肿瘤等多种疾病 ,改善人体微循环 ,并可用于生产中、老年人抗衰老、抗疲劳及增强免疫力的保健品 ,现已在医药、食品、工业等各个领域得到广泛的应用 ,并有着广阔的开发前景。     

蕾二歧灯芯柳珊瑚克生活性筛选及其低极性成分GC/MS分析

采用卤虫致死和细胞毒活性筛选模型,对蕾二歧灯芯柳珊瑚Dichotella gemmacea (valenciennes)乙醇提取物及各有机相进行了克生活性测定.结果表明,克生活性物质主要集中在石油醚相中.采用GC/MS技术对石油醚相进行了分析,鉴定了20个低极性化合物,主要为甾醇类、脂肪类化合物.推测甾醇类化合物是蕾二歧灯芯柳珊瑚的主要克生活性物质.     

天然海藻场沿岸表层沉积物有机质的分布特征与来源

海藻场是生物多样性最高的生态系统之一, 其内部的沉积物有机质是支撑海藻场生物多样性的重要物质基础之一。本研究以浙江省嵊山岛北部无人村沿岸的天然海藻场为研究对象, 在大型海藻凋落期6~8月采集沉积物和端元生物样本, 分析了沉积物样本的粒径组成、总有机碳 (TOC)、总氮(TN)、碳氮比值(C/N)和碳氮稳定同位素(δ¹³C和δ¹⁵N), 通过贝叶斯稳定同位素混合模型评估了沉积物有机质的来源及变化规律。结果显示, 1)海藻场沿岸沉积物中粉砂占比最大, 砂的占比最低, 沉积物类型为黏土质粉砂; 2)沉积物TOC、TN、C/N、δ¹³C和δ¹⁵N范围分别为0.70%~2.41%、0.11%~0.41%、5.53~6.48、–21.79‰~–19.60‰和1.56‰~4.26‰, 在空间分布上, TOC与TN含量均随离岸距离增加而下降; 3)沉积物粒径组成、C/N比值、δ¹³C和δ¹⁵N之间的关系显示沉积物有机质主要来源于大型海藻和浮游植物的混合贡献; 4)根据贝叶斯同位素混合模型计算结果显示, 大型海藻对沉积物有机质贡献率在2.30%~45.60%, 在空间分布上, 大型海藻对沉积物有机质的贡献率随离岸距离增加而下降; 5)海藻碎屑产生量和沉积物有机碳沉积量评估结果显示, 大型海藻产生的碎屑有机质中有11.98%进入海藻场及沿岸海域的表层沉积物中。本研究为评估海藻场碎屑的产生规模和时空分布, 以及渔业资源养护功能提供了数据支撑。     

养殖迁移对菲律宾蛤仔挥发性有机物质组成变化的影响

环境条件变化是造成贝类挥发性有机物质(VOCs)组成变化的主要原因。菲律宾蛤仔养殖生产中,常进行从开放式自然滩涂迁移至人工围塘养殖的活动。本文研究了这一过程前后菲律宾蛤仔(Ruditapes philippinarum)肌肉组织的VOCs组成特征、变化及其与环境因子相关性。结果显示:基于固相微萃取和气质联用技术,共鉴定出52种VOCs,分别属于醛、醇、酯、烃、呋喃、烷烃、烯、芳香烃、含硫和含氮化合物等。迁移前样本中,检出41种化合物,迁移至人工围塘养殖20 d后,检出32种。迁移造成了化合物种类数量降低、种类发生变化。醛、醇类的相对含量最高、迁移前后的变化尤为显著,呈现由醛高醇低的组成逆转为醇高醛低的特点。溶氧是影响VOCs组成变化及其醇、醛类差别的重要因子。饵料生物量、相对丰度和多样性与VOCs的组成具有显著相关性:自然滩涂微型真核生物多样性高但生物量和丰度相对低,人工围塘多样性低但生物量和丰度高,是VOCs组成差异的关键影响因子。本研究建立了贝类VOCs与关键环境因子的直接联系,为进一步解析贝类品质的环境关系、优化和调控养殖环境等研究提供了参考。     

一种短指软珊瑚Sinularia sp.克生活性筛选及其低极性成分GC/MS分析

采用卤虫致死和细胞毒活性筛选模型,对1种中国南海短指软珊瑚Sinularia sp.的乙醇提取物及各有机相进行了克生活性测定。结果表明,克生活性物质主要集中在石油醚相中。采用GC/MS技术,对石油醚相进行了分析,鉴定了15个化合物,主要为脂类和甾体类化合物;从石油醚相的甾醇部分鉴定了6个化合物,主要为麦角甾醇衍生物,占总甾醇含量的75.7%。推测甾醇类化合物是短指软珊瑚Sinularia sp.的主要克生活性物质。     

海水中大分子有机质对铂族元素的吸附动力学研究

Adsorption kinetics of the interaction between Pt, Pd and Rh(defined here as platinum group elements, PGEs)ions and macromolecular organic compounds(MOCs, 10 kDa), including humic acid, carrageenan and bovine serum albumin, and different cutoff fractions of natural organic matter(1 kDa and 3 kDa) obtained from seawater using centrifugal ultrafiltration devices were investigated. For a given element, all the adsorption kinetics did not reach equilibrium except the interaction between Pt and 1 kDa cutoff, and between Pd and humic acid.For all the tested MOCs, the adsorption kinetics could be divided into two stages, a rapid adsorption process in the first 8 h and the desorption stage after the first 8 h until the equilibrium. The change trend of partition coefficient(log_(10)K_d) values with experiment time was consistent with that of the kinetic curves. However, in the interaction between PGE ions and natural dissolved organic matter(NDOM), an obvious difference in the change trends of log_(10)K_d and kinetic curves was observed. It indicated that the partition behavior of PGE ions interacting with NDOM in seawater was a combined effect of different organic constituents. The adsorption and log_(10)K_d of PGEs in the 1 kDa NDOM fraction were higher and more stable than those in the 3 kDa NDOM fraction. The results also indicated that the 1–3 kDa NDOM may dominate the interaction between PGEs ions and NDOM. Moreover, no kinetic model could perfectly simulate the adsorption process. It indicated that the colloidal struction and morphology of MOCs or NDOM in seawater might be inhomogeneous. Hence, the interaction between PGE ions and organic matter in seawater was a complicated process and needs further research.     

The effects of dissolved organic matter on the aqueous partitioning of polynuclear aromatic hydrocarbons

The partitioning of six polynuclear aromatic hydrocarbons into aqueous solutions containing dissolved organic matter from various coastal environments was investigated by liquid chromatography. Specific hydrocarbon-organic matter interactions were observed. The greatest interactions occurred with the very low solubility hydrocarbons and with organic matter of terrestrial origin. Ultrafiltration experiments suggested that it was the relatively high (greater than approximately 500) molecular weight organic matter that was interacting with the hydrocarbons.     

Copper complexing ligands and organic matter characterization in the northern Adriatic Sea

The study on dissolved organic ligands capable to complex copper ions (L_T), surface-active substances (SAS) and dissolved organic carbon (DOC) in the Northern Adriatic Sea station (ST 101) under the influence of Po River was conducted in period from 2006–2008. The acidity of surface-active organic material (Ac_r) was followed as well. The results are compared to temperature and salinity distributions. On that way, the contribution of the different pools of ligands capable to complex Cu ions could be determined as well as the influence of aging and transformation of the organic matter. The L_T values in the investigated period were in the range of 40–300 nmol l⁻¹. The range of DOC values for surface and bottom samples were 0.84–1.87 mg l⁻¹ and 0.80–1.30 mg l⁻¹, respectively. Total SAS concentrations in the bottom layer were 0.045–0.098 mg l⁻¹ in equiv. of Triton-X-100 while those in the surface layer were 0.050–0.143 mg l⁻¹ in equiv. of Triton-X-100. The majority of organic ligands responsible for Cu binding in surface water originate from new phytoplankton production promoted by river borne nutrients. Older, transformed organic matter, possessing higher relative acidity, is the main contributor to the pool of organic ligands that bind copper in the bottom samples. It was estimated that 9% of DOC in surface samples and 12% of DOC in the bottom samples are present as ligands capable to complex copper ions.     

The application of isotopic and biogeochemical markers to the study of the biochemistry of organic matter in a macrotidal estuary, the Loire, France

The biogeochemistry of organic matter in a macrotidal estuary, the Loire, France, has been studied for two years during different seasons. Both particulate matter and sediment have been sampled in the riverine zone, in the maximum turbidity zone and in the ocean near the river mouth. Two techniques have been used: carbon isotopic ratio determination and analysis of lipid-marker signatures in the n-alkane, n-alkene and fatty acid series. For the period corresponding to the output of the maximum turbidity zone in the ocean, the complete change of organic matter, continental in nature in the inner estuary, pure marine in the outer estuary is well illustrated by the decrease of δ¹³C values and of carbon preference index of n-alkanes. Input sources of organic matter by continental plants, plankton and micro-organisms are discussed from biogeochemical-marker analyses data along with the processes of accumulation of particles and their evolution with the season. Some criteria for evidencing the nature of various organic-matter pools are assessed and compared in different chemical-marker series as follows: high molecular weight n-alkanes and fatty acids, perylene for continental imprints, polyunsaturated 18-, 20- and 22-carbon fatty acids, n-C₁₇, n-alkenes and squalene for algae imprints, branched iso and anteiso fatty acids, Δ11-C_18:1 for microbial imprints.     

The fate of terrestrial organic matter in two Scottish sea lochs

Sea lochs are zones of rapid organic matter (OM) turnover. Most of this OM is of allochthonous origin, being introduced into the lochs via freshwater input. In this study the behaviour of terrestrially derived OM was elucidated using a combination of parameters which indicate OM diagenesis in the near surface sediments from two Scottish sea lochs, Loch Creran and Loch Etive. Alkaline CuO oxidation was used to determine lignin phenols which serve as biomarkers for terrestrial OM in sediments. Stable carbon isotope, total carbon and nitrogen and total OM (including the labile and refractory fractions) compositions were also determined.