遮阴和盐分对银叶树幼苗光合特性与叶绿素荧光参数的影响

通过比较不同光和盐水平下银叶树(Heritiera littoralis)幼苗的叶绿素含量、光合光响应参数及叶绿素荧光参数的差异,探讨了遮阴和施盐处理下银叶树幼苗的光合生理及适应能力。以银叶树盆栽幼苗为研究对象,以全光无盐为对照,设置遮阴(遮光率为80%)与2.5%盐水处理,经60 d的处理,测定其光合光响应参数、叶绿素荧光参数及叶绿素含量。结果表明,在正常环境下,银叶树光饱和点(LSP)、光补偿点(LCP)及Chla/b分别为1023、28.8μmol·m^?2·s^?1及3.65,属阳性树种。在无盐条件下,遮阴处理导致了叶片叶绿素含量、表观量子效率(AQY)、PSⅡ潜在活性(Fv/Fo)、PSII最大光化学效率(Fv/Fm)及PSⅡ有效光化学量子产量(Fv'/Fm')的升高,却降低了Chl a/b、最大净光合速率(P′max)、LSP、LCP、暗呼吸速率(Rd)、初始荧光(Fo)、PSⅡ实际光合效率(ΦPSⅡ)、表观光合量子传递效率(ETR)、光化学猝灭系数(qP)及非光化学淬灭系数(NPQ)。在全光照或80%的遮阴环境下,盐胁迫均使得叶片叶绿素含量、光合光响应参数(AQY、P′max、LSP)及叶绿素荧光参数(Fm、Fv/Fo)显著下降(P<0.05);而在全光环境下,盐胁迫同样显著降低了Fv/Fm、ΦPSⅡ、ETR(P<0.05),但在遮阴环境下,盐胁迫并没有显著降低叶片Fv/Fm、Fv′/Fm′、ΦPSⅡ及ETR(P>0.05)。盐分对叶片叶绿素含量、光合光响应参数(AQY、P′max及LSP)及叶绿素荧光参数(Fo、Fm、Fv、Fv/Fo、ΦPSⅡ、ETR及NPQ)的影响高于光照,光和盐对叶绿素含量、光合光响应参数(AQY、P′max及LSP)及叶绿素荧光参数的影响没有交互作用。研究表明,银叶树幼苗表现出较高的耐阴性及对弱光的利用能力;盐胁迫使银叶树幼苗发生了明显的光抑制,PSII的光化学活性降低,过剩光能对光系统的破坏的风险增加,光能转换效率与电子传递能力下降,光合作用效率大幅降低。     

双波长标准加入法同时测定水中硝酸盐和亚硝酸盐

本文应用双波长标准加入法同时测定了硝酸盐和亚硝酸盐，在研究硝酸盐和亚硝酸盐紫外光谱的基础上，精确选择亚硝酸盐等吸收点波长２０２．５ｎｍ，２１６．５ｎｍ为测定波长。亚硝酸盐含量回归方程经推导得Ｃ＝－３．８４１＋１５６．６Ａ，相关系Ｒ＝１．０００。将该法用于合成样品及实际水样分析，所得结果较满意。     

拟面积多波长数据线性双组合解析萘,1—萘酚和2—萘酚同步荧光光谱的研究

本文研究了Δλ（λｅｍ－λｅｘ）为１３０ｎｍ和ＰＨ１２．０条件下，萘、１－萘粉和２－萘酚混合物的同步荧光光谱，获三者同步荧光峰信息，且萘被完全分辨，另外，提出用拟面积多波长线性双组合计算解析重叠的１－萘酚和２－萘酚同步荧光光谱，解析结果的精密度、组份间浓度比范围均较多波长线性回归、双峰增配平和一阶导数解析混合物同步荧光光谱结果为优。     

原子吸收分光光度法测定植株中钙、镁的几种样品前处理方法的比较

本文比较了原子吸收分光光度法测定植株中钙、镁的三种样品前处理方法：干友化法、１ｍｏｌ／ＬＨＣｌ振荡提取法（振荡法）和１ｍｏｌ／ＬＨＣｌ静止浸泡提取法（浸泡法）．结果表明，振荡法和浸泡法对钙的测定结果平均分别为干灰化法的１０１％和９２．０％，对镁的测定结果平均分别为１０３％和９７．６％．振荡法和浸泡法与干灰化法之间不存在显著性差异（α＝０．０５），它们之间有极显著的正相关性（相关系数在０．９９以上）．因此，在大批量样品的常规分析中，１ｍｏｌ／ＬＨＣｌ提取法可代替干灰化法．     

Mosaicism for trisomy 12: Four cases with varying outcomes

Trisomy 12 observed in chorionic villus sampling (CVS) may reflect generalized mosaicism or indicate mosaicism confined to only the placenta. In this report, four cases of trisomy 12 observed in CVS or cultured placental biopsies with varying outcomes are presented. Seven dinucleotide repeat polymorphisms for chromosome 12 were used to determine the chromosome 12 origins in the fetus or child and to delineate the mechanism(s) that gave rise to the trisomy. In two cases (cases A and C), the mosaicism was confined to the placenta, resulting in normal liveborns. Although, in one case, the molecular results suggested an apparent duplication of one paternal chromosome 12 in the placenta, normal biparental inheritance was found in the diploid fetal cell line in both cases. In two other cases (cases B and D), trisomy 12 was observed in both extraembryonic and fetal tissues. In one of these pregnancies, a child was born by Caesarean section at 37 weeks because of intrauterine growth retardation and oligohydramnios, and resulted in neonatal death. Molecular markers and fluorescence in situ hybridization (FISH) revealed low-level trisomy 12 mosaicism in the spleen. In the fourth case, fetal abnormalities were detected on ultrasound and low-level trisomy 12 mosaicism was observed in amniotic fluid cells using conventional cytogenetics and FISH. Molecular markers revealed a maternal meiosis I non-disjunction of chromosome 12 in DNA from a cultured placental biopsy. Although predicting the outcomes of pregnancies involving confined placental mosaicism remains difficult, molecular techniques are valuable tools for distinguishing uniparental from biparental disomy and mechanisms of mosaicism.     

Prenatal detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridization: A prospective study

A prospective study was undertaken to evaluate the use of fluorescence in situ hybridization (FISH) for the detection of trisomy 21 in interphase nuclei of uncultured amniotic fluid cells. Five hundred cases were analysed in situ and classified as normal or abnormal; the results were subsequently checked against the cytogenetic findings. Four hundred and ninety-three were correctly identified as normal with an 86·6 per cent average frequency of scored nuclei exhibiting two signals; six cases were correctly identified as trisomic for chromosome 21 with 81·7 per cent of scored nuclei exhibiting three signals; and one abnormal case involving an unbalanced chromosome 21·21 translocation was falsely scored as normal due to poor hybridization/detection efficiency. The method has been substantially improved and simplified so that it is suitable for the rapid detection of trisomy 21. As aneuploidy detection in interphase does not identify structural chromosome aberrations, it is not a substitute for fetal chromosome analysis.     

分光光度法测定嘉陵江中总磷

采用美国HACH公司DR/5000紫外可见分光光度计,及其专用试剂测定嘉陵江(南充段)上游、下游水样中总磷含量.测定总磷含量(以PO3-4计)适用范围(0.06 mg/L～3.50 mg/L),精密度和灵敏度较好,准确度高,标准物质的回收率都近于100%.对于样品中存在的干扰因素进行了有效的消除.简化了实验操作过程,使测试方法更加简便、快捷、试剂用量少,该方法通过美国环保局(USEPA)认可.     

Comparative analysis of the structure of carbon materials relevant in combustion

The determination of the structure of carbon materials is an analytical problem that join the research scientific communities involved in the chemical characterization of heavy fuel-derived products (heavy fuel oils, coal-derived fuels, shale oil, etc.) and of carbon materials (polycyclic aromatic compounds, tar, soot) produced in many combustion processes.

The knowledge of the structure of these “difficult” fuels and of the carbon materials produced by incomplete combustion is relevant to research for the best low-environmental impact operation of combustion systems; but an array of many analytical and spectroscopic tools are necessary, and often not sufficient, to attempt the characterization of such complex products and in particular to determine the distribution of molecular masses.

In this paper the size exclusion chromatography using N-methyl-pyrrolidinone as eluent has been applied for the characterization of different carbon materials starting from typical carbon species, commercially available like polyacenaphthylene, carbon black, naphthalene pitch up to combustion products like soot and soot extract collected in fuel-rich combustion systems. Two main fractions were detected, separated and molecular weights (MWs) determined by comparison with polystyrene standards: a first fraction consisted of particles with very large molecular masses (>100 000 u); a second fraction consisted of species in a relatively small MW range (200–600 u). The distribution of these fractions changes in dependence on the carbon sample characteristics.

Fluorescence spectroscopy applied on the fractions separated by size-exclusion chromatography has been used and comparatively interpreted giving indications on the differences and similarities in chemical structure of such different materials.     

利用分子信标和EXO III放大荧光信号快速检测Ag+

设计新型的DNA探针,其主要功能区域包含适配体区域和分子信标互补区域;当无靶标存在时,羧基荧光素（FAM）的荧光被黑洞猝灭基团（BHQ）猝灭,加入靶标后,Ag⁺与适配体区域特异性结合,使得分子信标与其互补区域发生结合,加入EXO Ⅲ后,分子信标被酶解,从而释放Ag⁺/DNA探针复合物用于下一轮反应,同时产生大量的FAM,因此,可以通过荧光的增强来定量检测靶标的含量.评价了该方法的灵敏度和选择性,探究它在实际样品中的表现能力.结果表明,适配体区域与分子信标间隔2个碱基的DNA探针与分子信标结合效果最好,检测的信噪比最大.该方法对Ag⁺的检测最低下限（LOD）为0.1nmol/L,在0.5~200nmol/L范围内,荧光值与靶标浓度成线性关系（R²=0.994）.对实际样品的检测在20~200nmol/L范围内呈线性关系（R²=0.998）,且能很好的从混合样品中区分10nmol/L Ag⁺.该研究建立的快速检测Ag⁺方法具有良好的线性定量能力和操作性能,且灵敏度高、特异性强,可满足现实的需求.     

黄河干流宁蒙段溶解性有机物组分特征及其与金属离子的相关性

溶解性有机物(dissolved organic matter,DOM)是天然水体的重要组成部分,由于化学极性及所含的官能团不同,其在水体中的化学行为也不同.本研究以黄河干流宁蒙段为研究对象,于2015年4月采集了下河沿至头道拐沿程7个断面的水样,采用XAD系列树脂将DOM分为疏水性酸(hydrophobic acid,HOA)、疏水性碱(hydrophobic base,HOB)、弱疏水性酸(weak hydrophobic acid,WHOA)和亲水性物质(hydrophilic matter,HYI)这4个组分,探讨了DOM组分含量、荧光峰值及其与Pb、Zn、Cu、Cr、As这5种金属离子之间的相关性.结果表明,黄河宁蒙段DOM总量由下河沿至头道拐沿程逐渐增加.各断面DOM腐殖化程度较低,以亲水性的蛋白质类小分子物质(HYI)为主,疏水性酸(HOA)次之,这与黄河沿岸排污导致内源作用增强有关.三维荧光光谱中类腐殖质和类蛋白质荧光峰型显著,且类腐殖质峰沿程逐渐增强,进一步证实了内源污水输入的影响.SPSS相关性分析结果表明,DOM与5种金属离子呈现出不同程度的相关性,其中与Cu离子显著相关;4种组分中HYI与Cu离子的相关性最强,说明二者在迁移转化过程中存在显著相互作用.进一步研究发现,芳香蛋白类物质荧光峰强度随Cu离子浓度的升高而降低,这可能是Cu与亲水性组分中的芳香类蛋白质发生络合产生荧光淬灭效应,从而导致荧光强度降低.