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1.
阎雪姣  王江涛 《海洋科学》2012,36(5):103-108
对测量海水中总溶解氮(TDN)的两种常用方法——高温燃烧法和过硫酸钾氧化法进行了比较。结果表明,两种方法在空白、精密度和准确度实验中不存在显著差异。对不同化合物的回收率均在92%~107%之间,加标回收实验回归曲线的斜率分别为0.93和0.92。对于现场海水样品的测定结果,两个断面拟合的斜率分别为0.92和0.97。HTC法比PO法对实际海水样品的氧化效率略高,在操作上也更方便、快捷。因此,高温燃烧法更适合海水中总溶解氮(TDN)的测定。  相似文献   

2.
采用显微镜细胞计数和麻痹性贝毒的高效液相色谱分析方法,通过对比磷酸二氢钾、磷酸甘油和三磷酸腺苷(ATP)等含磷营养物质对微小亚历山大藻生长和毒素产生的影响,研究了微小亚历山大藻对不同类型含磷营养物质的利用情况.结果表明,在磷限制条件下,加入磷酸二氢钾、磷酸甘油和ATP均能促进微小亚历山大藻的生长,所获得的最大藻细胞密度分别为22700、28400和27800藻细胞/ml,对数期生长速率分别为0.12/d、0.14/d和0.15/d,溶解态有机磷对藻生长的促进作用稍好于溶解态无机磷.三种含磷营养物质对毒素产生的效应没有明显差别,稳定期藻细胞毒素含量分别为22.87、23.98和21.80fmol/cell.磷限制对毒素组成的影响很大,磷限制条件下膝沟藻毒素GTX1/4的含量占绝对优势,GTX2/3含量很少.在添加含磷营养物质后,GTX1/4所占比例降低,GTX2/3比例增加,说明磷限制显著改变了微小亚历山大藻的毒素组成.对藻体碱性磷酸酶活性分析的结果显示,磷限制组具有最高的碱性磷酸酶活性,添加有机磷化合物实验组的碱性磷酸酶活性显著高于添加无机磷化合物的实验组.研究结果表明,微小亚历山大藻可以利用实验中采用的无机磷化合物和有机磷化合物,但其利用溶解态有机磷化合物的机制尚不清楚,可能是通过诱导合成碱性磷酸酶来水解培养基中的溶解态含磷有机物,从而释放无机磷酸盐用于藻细胞的生长.  相似文献   

3.
海水中总氮和总磷的同时测定   总被引:24,自引:0,他引:24  
早期总氮和总磷的过硫酸钾法氧化分析分别是在碱性和酸性介质中进行[1,2],样品分别保存,然后分别氧化测定,工作较繁琐。1977年Koroleff用过硫酸钾氧化法同时氧化水体中的总氮和总磷,使样品的保存和氧化分析工作简化。1981年Valderrama对该方法测定天然海水中的总氮和总磷做了进一步研究,总氮和总磷同时氧化后,水样中的硝酸盐和磷酸盐用手工分别进行分析。Walsh1989年和Karl等1993年曾采用UV光氧化法对海水中总溶解氮和总溶解磷进行同时氧化后,用自动分析对氧化后的无机氮和磷进行…  相似文献   

4.
海水化学需氧量(COD)是海水水质的重要检测指标,然而在河口及近岸海域的低盐环境下,由于受到Cl~-的干扰,其实测值无法准确反映近岸盐度较低海域的有机污染程度。本文研究了不同盐度条件下,Cl~-对以葡萄糖为底物的COD测定的影响过程,对比分析了Cl~-对COD和淡水碱性高锰酸盐指数(COD_(Mn))测定的影响程度,以期获得这两种方法测定结果可对应的依据。结果表明:海水COD测定方法在S≈25~35区间内是稳定的,但在S≈0~25区间,测定方法的氧化率随Cl~-浓度的降低而下降,而且有机物浓度越低氧化效率越低。Cl~-对海水COD测定的影响发生在碱性KMnO_4加热氧化有机物阶段。淡水碱性COD_(Mn)测定方法在S≈0~10区间内的氧化效率与海水COD方法在S≈25~35区间内的氧化率相当,并初步提出了以葡萄糖为底物的低盐区COD测定值的校正式,这对于准确认识盐度较低的河口及近岸海域有机污染程度是非常有益的。  相似文献   

5.
依据国内外最新研究成果,初步讨论了氧化还原敏感性微量元素(RSE)Re、Cd、Mo、U、V等的地球化学行为,其中包括海洋沉积物中RSE的来源、RSE在缺氧和无氧海区的沉淀富集机理及其环境指示意义。在此基础上讨论了利用RSE研究氧化还原环境时应注意的一些问题。RSE的沉淀富集机制不尽相同,但具有以下共同特点:①对底层海水的溶解氧浓度敏感。在正常溶解氧条件下,氧化还原敏感性微量元素在海水中呈溶解态稳定存在,而当底层海水处于缺氧或无氧条件时容易发生还原。②当底层海水处于缺氧或无氧条件时,经过沉积物—海水界面过程,受缺氧程度不同的制约,海水中呈溶解态的RSE依次在沉积物中沉淀,出现不同程度的富集。③持续还原条件下,RSE在沉积物中稳定存在;受氧化作用后,容易在沉积物中发生二次迁移和重新富集。不同的RSE其氧化还原电位不同,在氧化还原序列中的位置不同,Re在U之后Mo之前发生还原。因此,RSE在海洋沉积物中的不同富集特征和富集程度可作为还原程度指标研究底层海水的缺氧程度和底质的氧化还原环境。研究RSE的氧化还原环境指示意义,必须对RSE陆源碎屑来源组分进行剔除,同时,还应充分注意到还原沉积区发生氧化后,RSE在沉积物中会发生重新迁移和二次富集。  相似文献   

6.
以酶学分析方法研究了不同温度、pH及摄食后不同时间扁额原细首纽虫蛋白酶活性的变化.结果表明,扁额原细首纽虫蛋白酶活力在pH为3和10时出现2个峰值,酸性条件下其蛋白酶的活性明显高于碱性条件.在20~80 ℃温度范围内,纽虫酸性和碱性蛋白酶活性表现出2种不同的变化趋势.酸性蛋白酶活力在50 ℃达到最大值;而碱性蛋白酶活力在40 ℃达到最大值,50 ℃酶活性急剧下降,对高温比较敏感.扁额原细首纽虫在摄食后,酶活力有明显变化,酸性蛋白酶在摄食后2 h达到最大值,之后下降,摄食后8 h达到最低水平,之后又有所回升.而碱性蛋白酶活性在摄食后8 h达到最大值,16 h后维持在较低水平.  相似文献   

7.
海水溶解有机物(dissolvedorganicmatter,DOM)中含有的生物活性物质在海洋生态系统中作用巨大,但因缺乏适合的分离提取方法而严重阻碍了对其不同组分在生态系统中作用的探索。固相萃取法对富集提取海水DOM十分有效,在用其提取海水DOM时,海水pH对活性物质提取效果的影响很大,但目前针对海水的这种影响尚存在很大争议。本文以天然近海海水作为基质,探究不同pH条件下用亲水-疏水平衡(hydrophilic-lipophilicbalanced,HLB)固相萃取小柱萃取海水中活性分子的提取效率,并使用高效液相色谱-四极杆飞行时间质谱(HPLC-Q-TOF-MS)在负离子(ESI-)模式下检测解析提取物的组成。研究结果表明,当海水样品pH为中性和强酸性时都能获得较好的提取效率,随着pH的降低,提取物质谱的整体响应值降低,但可识别的谱峰数目增加,提取出有机物的分子量和性质差异都更广泛。分析提取物分子在范克雷维伦(van Krevelen)图和质荷比-氢碳比(m/z-H/C)图上的分布发现,中性条件适合提取饱和度较高的小分子化合物,而具有生物活性的带有不饱和基团的化合物及蛋白质、糖类等生物大分子在强酸性提取条件时提取效果和分辨率更好。综合提取效率、有效峰数目和分子组成特征考虑,用HLB固相萃取小柱提取近海海水中的小分子活性物质时,将海水样品pH调节为2较为适宜。  相似文献   

8.
高温燃烧法测定海水中的溶解有机碳   总被引:5,自引:2,他引:3  
1997年5月在莱州湾,1997年7月在东海,1997年11月在胶州湾采集了海水样品,高温燃烧法测定了这些水样中的溶解有机碳浓度,了系统空白和标准曲线的选择对高温燃烧法测定结果的影响,并与紫外/硫酸钾法的测定进行了比较。  相似文献   

9.
制备了活性半焦催化剂用于在低温下将NO氧化为NO2。通过水热活化、高温活化、酸活化、碱活化以及组合活化等多种活化方法对原半焦进行活化改性,以提高半焦的催化氧化性能。利用酸碱滴定、Boehm滴定、SEM、BET、FT-IR等方法对活性半焦的物化性质进行了表征。采用固定床反应器测定活性半焦催化氧化NO的能力,其反应条件为:温度70℃、空速600 h-1、O2和NO浓度分别为5%和443 mg/m3。将活性半焦催化氧化NO的催化性能与其物化性质进行了关联,结果表明:半焦上的羰基官能团和碱性官能团共同作用于NO的吸附氧化过程,NO在羰基上被吸附并氧化,碱性官能团则协助氧化产物NO2迁移出羰基活性位并将NO2储存在碱性官能团上,使羰基活性恢复。根据以上理论所制备的经过碱活化和高温活化的催化剂硝容最大,可达1.01%。  相似文献   

10.
海水中痕量DMS和DMSP分析方法的研究   总被引:7,自引:1,他引:6       下载免费PDF全文
二甲基硫(DMS)是海洋排放的占优势地位的生源硫气体,其在大气中的氧化产物能够影响到环境酸化和世界的气候变化.因此, 测定海水中的DMS对于准确地评价其在全球硫循环所起的重要作用具有重要意义.本文中作者研究了海水中DMS的痕量分析技术.海水中的DMS首先采用气提-冷阱捕集技术进行预浓缩, 然后用带有火焰光度检测器的气相色谱(GC-FPD)进行分析.该方法的精确度在5%以内, 平均回收率为85.6% (82.8%-90.5%), 最小检出限为0.15 ng S.β-二甲基巯基丙酸内盐(DMSP)的分析是通过将其在碱性溶液中分解成DMS来进行.作者采用此方法实测了黄海中DMS和DMSP的含量, 获得了理想的结果.  相似文献   

11.
Several methods for analysis of dissolved total phosphorus in seawater were reviewed. Discussions were focused on UV irradiation and persulphate oxidation methods which are the most popular dissolved organic phosphorus determination methods presently. The compounds used for the phosphorus recovery test were categorized into three groups according to their chemical structure. It was found that low power UV irradiation can decompose P-O-C or P-C bonds efficiently but may be inefficient for P-O-P bonds. Heating-bath in acid condition is useful for decomposing P-O-P bonds. Using the continuous flow analysis system (Auto-analyzer Ⅱ), UV digestion and heating-bath, series experiments were carried out based on the above analysis. Eleven model compounds were employed for the phosphorus recovery test and the factors influencing the decomposition efficiency of dissolved compounds containing phosphorus were clarified. Finally, the optimal design for determination of dissolved total phosphorus in seawater based on the routine continuous flow analysis system was presented. For the organic mono-phosphate, the recovery is more than 90% and a recovery of 33%~51% was obtained for inorganic or organic polyphosphates. Up to now, this is the highest decomposition efficiency for dissolved phosphorus based on the continuous flow analysis system.  相似文献   

12.
We developed a simple and reliable method which allows simultaneous determination of organic forms of carbon (DOC), nitrogen (DON) and phosphorus (DOP) dissolved in seawater. Conversion of dissolved organic matter (DOM) to inorganic products (carbon dioxide, nitrate+nitrite and soluble reactive phosphate) is performed by a persulfate wet-oxidation in low alkaline condition. After oxidation, the concentration of the inorganic products dissolved in the sample was measured automatically by colorimetry using a 3-channel Technicon AutoAnalyzer system. A number of pure organic compounds were tested in the concentration range encountered in coastal and open ocean, indicating a high efficiency of the digestion procedure. The recovery range is similar to that obtained by other wet-oxidation procedures and by high-temperature catalytic oxidation techniques. Direct comparisons with usual methods used for separate determination of DOC, DON and DOP indicated a high efficiency of the procedure. Reproducibility tests demonstrated a very good precision (around 5%) for lagoonal and coastal waters, while precision was sometimes around 10–25% in oligotrophic oceanic waters, especially for DOP where values approached limits of detection for measuring phosphate. This method is highly suitable for routine analysis and especially appropriate for shipboard work.  相似文献   

13.
Three methods for the determination of dissolved organic carbon in seawater were compared. Samples were analysed using persulphate oxidation, high-temperature combustion, and ultraviolet photo-oxidation. The dissolved organic carbon content of the seawater samples ranged from 0.6 to 1.6 mg C/I. This study shows that results of high-temperature oxidation and photo-oxidation procedures differ by less than 5%, whereas results with persulphate oxidation are about 15% less than those obtained with the high-temperature oxidation. The relative merits of each of the oxidation techniques for the determination of organic matter in seawater are discussed.  相似文献   

14.
对紫外(UV)光降解-过硫酸钾方法分析溶解有机磷的条件进行比较分析,在UV/加热条件下溶解有机磷的氧化率最高.进一步考察氧化剂的酸碱性和浓度对溶解有机磷氧化率的影响.Cl-和海水介质可以使溶解有机磷的氧化率显著降低.可以通过改变UV灯的功率、反应时间、反应温度、氧化剂等条件提高溶解有机磷的氧化率.  相似文献   

15.
利用切向超滤(cross-flow ultrafiltration)技术对海水中胶体有机碳(COC)和真溶解有机碳(UOC)进行了分离,并分别用高温燃烧法和紫外/过硫酸钾法对胶体有机碳和真溶解有机碳进行了测定。测定结果表明,切向超滤能定量分离海水中的胶体有机碳,高温燃烧法和紫外/过硫酸钾法对胶体有机碳和真溶解有机碳的测定结果没有明显的系统误差,表明这两种方法的氧化效率基本相同,胶体粒子的存在,对紫外/过硫酸钾法的氧化效率没有显着影响。  相似文献   

16.
We measured tissue phosphorus content of high and low intertidal Hormosira banksii to test the hypothesis that tissue phosphorus content would be greater in individuals from the low intertidal because of greater total uptake associated with longer immersion in seawater. Moreover, we predicted that tissue phosphorus would be greater at sites where the seawater contained higher phosphate concentrations. There was a positive, linear relationship between local seawater phosphate concentrations and tissue phosphorus content of H. banksii from high and low intertidal zones at six different sites in winter. However, there were no comparable relationships in summer, even though the range of seawater phosphate concentration was similar in both seasons. The phosphorus contents of low intertidal H. banksii were significantly greater than high intertidal H. banksii in winter, but not in summer. Reasons for these differences may be related to greater access to seawater phosphate in low intertidal algae (than those in the high intertidal) in winter, followed by greater utilisation of the internal phosphorus between winter and summer, due to faster growth rates in the low intertidal.  相似文献   

17.
We describe an investigation into the reactivity of dissolved organic carbon (DOC), produced from marine algae, to conventional persulphate and ultraviolet (UV) oxidation methods. Marine algae were grown in batch culture in the presence of 14C bicarbonate and filtered samples of the phytoplankton dissolved organic carbon (PDOC) were oxidized with persulphate and UV techniques. The amount of fixed label found in solution after the oxidation procedures was compared with the initial amount of labelled DOC. Marine algae examined in this way included: the diatoms, Chaetoceros gracilis, Skeletonema costatum, Phaeodactylum tricornutum; the flagellate, Isochrysis galbana; and the cyanobacterium, Synechococcus strain DC2. It was found that 5–18% of the DOC produced by these phytoplankton resisted persulphate oxidation. Samples were also measured for their resistance to UV oxidation by an autoanalyzer method. It was found that 15–27% of these samples resisted UV oxidation. However, 95% of PDOC was oxidized after exposure for 6 h to high intensity UV irradiation using a variable exposure time system. P. tricornutum and Synechococcus PDOC samples were ultrafiltered into low molecular weight (< 10 000 Da) and colloidal (> 10 000 Da) size fractions. Both species produced mainly (> 68%) low molecular weight material. Slightly greater resistance to persulphate oxidation was generally found for the colloidal Synechococcus PDOC (15–22%) than for the low molecular weight material (14–17%). However, the opposite was found for the P. tricornutum PDOC which generally showed less resistance for the colloidal fraction (5–12%) than for the low molecular weight fraction (10–15%).Experiments were also conducted to determine the effects of short-term (days) and long-term (months) ageing of PDOC solutions in the presence of microbial populations from coastal seawater. Long-term ageing decreased the amount of PDOC that resisted oxidation in all cases. However, the fraction of PDOC resisting persulphate oxidation increased by small amounts over a short-term experiment. Increased resistance was attributed to preferential degradation of biologically and chemically labile components of PDOC by bacteria.The percentages of phytoplankton-produced (and microbially aged) DOC found in this study to resist UV or persulphate oxidation were low (5–27%), compared with those values (50–65%) reported for DOC in surface seawater on the basis of recent high temperature catalytic oxidation analyses.  相似文献   

18.
河口潮滩沉积物磷的季节性累积和生物有效性   总被引:2,自引:0,他引:2       下载免费PDF全文
对长江口潮滩表层沉积生磷的赋存形态和含量的研究表明,碎屑态磷为沉积物中磷的主要形态,约占总磷的62.52%;铁结合态磷和有机磷次之,分别占总磷的18.06%和14.69%;自生磷灰石加钙结合态磷和吸附态磷最少。综合研究区内的各种理化条件,指出弱吸附态磷、铁结合态磷和有机磷是长江口潮滩潜在生物可利用磷,约占总磷的33.16%,是导致水体富营养化的潜在因素。上覆水的盐度效应是影响沉积物铁结合态磷含量的关键性因子;而自生磷灰石加钙结合态磷的含量变化则与上覆水的温度、溶氧量及沉积物有机质的分解有关;有机磷在时间和空间尺度上都存在较大变化,主要与潮滩生物动态过程,即磷的再矿化有关。  相似文献   

19.
南海海域海水中各形态磷的化学分布特征   总被引:6,自引:0,他引:6  
根据1998年7月和1999年1月两个航次的调查资料,对南海水体中磷的含量分布以及夏、冬季变化规律进行了探讨.结果表明,南海表层水体中磷酸盐夏季含量明显低于冬季,夏季平均含量为0.004μmol/dm3,而冬季为0.35 μmol/dm3;有机磷含量夏季高于冬季,含量分别为0.12,0.04 μmol/dm3;总磷含量的季节变化与无机磷酸盐类似,夏、冬季含量分别为0.22,0.61 μmol/dm3.在垂向分布上表层50 m水柱中PO43--P,总溶解态磷和总磷含量最小,随水深增加基本上呈线性快速增加,至500 m增加减缓,1 000 m左右为最大含量,然后随着水深略有下降.在夏季垂直分布比较典型,不同站位在一水深的含量离散性小,而冬季PO43--P,总溶解态磷和总磷的垂直分布则显得离散性大,尤其是PO43--P分布在200 m左右出现最大值,说明当年冬季南海各区域存在着较大水文、生物差异,很大的影响了化学环境的变化.在南海表层水中通常以有机磷占优势,在150 m深处以下的水中则以无机磷为主.深水中溶解的有机磷含量一般随水深减少.夏季的有机磷明显高于冬季,表明夏季的生物作用强烈.  相似文献   

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