江苏下扬子区牙形刺荧光强度与色变指标的相互关系

本文通过对江苏下扬子地区不同色变指标牙形刺的荧光强度测试,发现随牙形刺色变指标的增加,牙形刺荧光强度减弱,从而建立了牙形刺荧光强度与色变指标的相互关系,为江苏下扬子区海相地层的有机质成熟度评价提供一个新的参数。     

广西天等把荷剖面早泥盆世晚埃姆斯期的牙形刺北大核心CSCD

广西天等把荷剖面下泥盆统埃姆斯阶产较丰富的Polygnathus属牙形刺化石。经详细鉴定,共识别出Polygnathus inversus,Pol.gilberti,Pol.laticostatus,Pol.linguiformis bultyncki,Pol.nothoperbonus,Pol.perbonus,Pol.serotinus,Pol.vigierei等11种(含1个未定种和2个相似种)。根据牙形刺的特征和地层分布,自下而上划分为3个牙形刺带,即nothoperbonus带、inversus带和serotinus带。在系统分类研究的基础上,根据剖面中牙形刺产出层位及齿台口面和反口面特征分析,Pol.serotinus可能由Pol.vigierei通过外齿台边缘的抬升、外侧近脊沟的变宽变深以及齿台前缘的逐渐平行演化而来,Polygnathus属反口面基腔翻转的特征最早出现在Pol.nothoperbonus演化阶段。     

微体古生物学发展的新成果──介绍《下扬子地区牙形刺》

微体古生物学发展的新成果──介绍《下扬子地区牙形刺》由王成源教授主编,丁连生、段金英等十几位作者共同撰写的《下扬子地区牙形刺》一书即将由科学出版社出版。这是一部下扬子地区牙形刺化石的全面系统的总结。书中收集了下扬子地区７６条剖面、７８４０个牙形刺样品...     

内蒙古乌海大石门奥陶系牙形刺和Histiodella动物群发现的意义

本文描述了内蒙古乌海大石门剖面奥陶系的牙形刺动物群:下克里摩里组主要有Histiodella kristinae,H.holodentata,H.wuhaiensis sp.nov.,Polonodus newfoundlandensis和Paroistodus horridus等,应归属于中奥陶统达瑞威尔阶(Darriwilian)之Histiodella kristinae带,并在同一剖面上与笔石Pterograptus elegans带和Didymograptus murchisoni带下部相当;下克里摩里组顶部产Histiodella kristinae,Baltoplacognathus cf.reclinatus,Periodon aculeatus和Protopanderodus rectus等,所以大石门剖面的Histiodella kristinae带顶部可能已与北欧Pygodus serra带之底部相当;乌拉力克组底部的砾状灰岩透镜体产有牙形刺Pygodus anserinus?,Protopanderodus liripipus,Yangtzeplacognathus protoramosus和Dapsilodus viruensis等,其中Pygodus anserinus?Pa分子(器官种的一组成分子)的口面瘤齿列的瘤齿比较粗糙,与典型的Pygodus anserinus稍有不同,且在牙形刺十分丰富的样品中仅有一枚此种之Pa分子,所以本文尚有疑问地把这层砾状灰岩归入Pygodus anserinus带,同时不能排除把它归入Pygodus serra带顶部Yangtzeplacognathus protoramosus亚带的可能。由于此剖面牙形刺化石与丰富的笔石共生,为牙形刺带与笔石带的精确对比提供了直接证据。Histiodella动物群在此剖面的发现,不仅具有十分重要的地层意义,而且具有明显的岩相古地理意义。本文详细描述了新种Histiodella wuhaiensis并讨论了Histiodella属5个种之区别。     

吉林李家窑范家屯组中的二叠纪北温带牙形刺动物群

在吉林省九台市三台乡李家窑附近的二叠系范家屯组中采到一特殊的牙形刺动物群。多数牙形刺都较小,锯齿发育,齿脊细齿不愈合。由一些未见报道的新分子组成。本文描述了４个新种（Ｍｅｓｏｇｏｎｄｏｌｅｌｌａ ｃｈａｎｇｃｕｎｅｎｓｉｓ ｓｐ．ｎｏｖ．,Ｍ．ｊｉｌｉｎｅｎｓｉｓ ｓｐ．ｎｏｖ．,Ｍ．ｍｕｌｔｉｓｅｒｒａｔａ ｓｐ．ｎｏｖ．,Ｍ．ｐｓｅｕｄｏａｌｔｕｄａｅｎｓｉｓ ｓｐ．ｎｏｖ．）和３个未命名新种     

微体古生物学发展的新成果——介绍《下扬子地区牙形刺——生物地层与有机变质成熟度的指标》一书

由王成源教授主编、丁连生、段金英等十几位作者共同撰写的《下扬子地区牙形刺》一书即将由科学出版社出版。这是一部下扬子地区牙形刺化石的全面系统的总结。书中收集了下扬子地区76条剖面、7 840个牙形刺样品的资料;建立了从寒武纪至二叠纪的53个牙形刺化石带或组合带;依据牙形刺化石修订了传统的地层界线;并对全球二叠纪地质年表提出了新的见解,且在下扬子区首次发现了志留纪牙形刺化石。全书共约     

安徽石台奥陶纪弗洛期—大坪期牙形刺多样性的演变

基于安徽石台栗阳柳树亭下、中奥陶统紫台组牙形刺的系统研究,对该地区早奥陶世弗洛期一中奥陶世大坪期牙形刺多样性演变作了初步分析,发现牙形刺的简单分异度在弗洛晚期Oepikodusevae带达到峰值,有17属20种。之后,牙形刺分异度呈下降趋势。演变的总体趋势与湖北宜昌地区同期牙形刺的研究结果一致,其峰值出现的时间（Oepikodusevae带,相当于笔石Didymograptellus eobifidus带上部,Corymbograptusdeflexus带,及Azygograptussuecicus带下部）与华南上扬子区腕足动物宏演化趋势（首次峰值出现在Didymograptelluseob—ifidus带）大体相似,但比三叶虫多样性演变在奥陶纪的首次峰值（出现在Exigraptus clavus带）早,比扬子台地笔石多样性演变的首次峰值（在Acrograptusfiliformis带和Didymograptelluseobifidus带下部）晚。分析显示,该地区早、中奥陶世牙形刺多样性演变与海平面变化存在密切关联。     

滇西北石炭系和二叠系牙形刺序列

本文论述了云南西北部宁蒗县石炭系、二叠系尖山营剖面的牙形刺研究成果。共划分出17牙形刺带。由于采样系统,牙形刺序列连续,而且与国内外的牙形刺带可以对比,为本区生物地层的研究提供了可靠的古生物学基础。尖山营剖面牙形刺众多,同时含有丰富的珊瑚、腕足类,(竹蜓)类、菊石等化石,是研究不同化石门类生物地层对比的理想剖面;此剖面的进一步工作,将为不同相区地层对比提供更为可贵的资料。值得注意的是,本区石炭系、二叠系的界线,尚待深入研究,二叠系的底界很可能     

晚三叠世台形牙形刺分子的演化

晚三叠世台形牙形刺分子属有Ｐａｒａｇｏｎｄｏｌｅｌｌａ,Ｍｅｔａｐｏｌｙｇｎａｔｈｕｓ,Ａｎｃｙｒｏｇｏｎｄｏｌｅｌｌａ和Ｅｐｉｇｏｎｄｏｌｅｌｌａ。这些属都源于中三叠世,可能来自同一根源──Ｎｅｏｇｏｎｄｏｌｅｌｌａ,但有两个不同的演化趋向。本文认为这些台形分子分类演化上最重要的形态特征仅是一些微小的变化,如齿台下方后龙脊─基部附着面,基穴和环台面的细部变化。对Ｍｅｔａｐｏｌｙｇｎａｔｈｕｓ属台形分子的发展演化作了专门讨论,指出了晚三叠世台形牙形刺分子的演化系统。     

日本志留纪至三叠纪牙形刺生物地层

本文系统地回顾了日本志留纪至三叠纪牙形刺研究的历史和现在的成果。志留纪牙形刺只有少数零星的报道,没有建立化石带;早泥盆世已建立了５个牙形刺组合,没有中、晚泥盆世的记录;石炭纪有８个牙形刺带,其中晚石炭世３个牙形刺带;二叠纪５个牙形刺带或动物群,其中,中、晚二叠世各１个带（动物群）;三叠纪可划分出１４个牙形刺带。     

Flow system fluorescence polarization measurements on fluorescein diacetate-stained EL4 cells.

We have adapted a multiparameter cell sorter to measure the distribution of fluorescence polarization in cell populations. Measurements carried out on EL4 cells show that the percent polarization of fluorescein fluorescence decreases with increasing fluorescence intensity. This inverse relationship between polarization and intensity is shown both within the cell population and by the average values of the two quantities during both the increase and decrease of fluorescence intensity. The quantitative relation between intensity and polarization is different in hypertonic than in isotonic media. These results suggest that polarization measurements carried out at a fixed time after incubation of cells with fluorescein diacetate, which is converted to fluorescein within the cells, may depend in part on the rate of fluorescein accumulation, and that agents that have been reported to change the polarization of fluorescein in living cells may do so by changing the kinetics of fluorescein accumulation.     

ATP稳定肌浆网膜蛋白色氨酸相关构象的机理的探讨

在无ＡＴＰ存在时,带相同正电荷、但饱和不同的两种胺类两亲物,即Ｃ１８饱和的硬脂胺与单不饱和的油胺引起肌浆网蛋白内源荧光强度降低,当ＡＴＰ或一些阴离子化合物先与肌浆网作用,再加入硬脂胺或油胺,则肌浆网蛋白内源荧光下降幅度明显减小,即存在拮抗作用。腺苷对硬脂胺或油胺均无此拮抗作用。肌浆网与油胺先保温,再加入ＡＴＰ或阴离子化合物,ＡＴＰ仍有拮抗,阴离子化合物对油胺则无拮抗作用。然而在肌浆网钙泵蛋白上存在     

Dependence of Ca2+ release from intracellular stores on NADH and FAD levels in fertilized and unfertilized bovine oocytes

Relation between NADH and FAD concentrations and the quantity of calcium released from intracellular stores in fertilized and unfertilized bovine oocytes was investigated using luminescent analysis. Inhibition of Ca2+ exit from intracellular stores was detected in degenerative oocytes at metaphase II and 2-cell embryos. The intensity of both NADH and FAD fluorescence increased in 2-cell degenerated embryos, whereas the increase in only NADH fluorescence intensity occurred in degenerated oocytes at metaphase II stage. Degeneration exerted no influence on NADH fluorescence intensity or Ca2+ exit from intracellular stores, whereas a decreased FAD fluorescence intensity was noted in degenerated pronuclei. The obtained data testify that in degenerated zygotes and early embryos Ca2+ release may occur from different intracellular stores.     

Fluorescence of Tb3 complexes with metaphase chromosomes of mink fibroblasts

The fluorescence of the Tb3+ complex with metaphase chromosomes of mink fibroblasts was studied. It was shown that the fluorescence intensity of this complex is 6.5 times as high as that of the Tb3+-native DNA complex. The fluorescence of the chromosome-Tb3+ complex is predominantly determined by chromosomal DNA. The high intensity of fluorescence may be due to partial disturbances in the secondary structure of DNA during folding of the metaphasic chromosome.     

An evaluation of N-phenyl-1-naphthylamine as a probe of membrane energy state in Escherichia coli

Colicin E1 and the uncoupler of oxidative phosphorylation, trifluoromethoxy-carbonylcyanidephenylhydrazone (FCCP), cause an increase in the fluorescence intensity of N-phenyl-1-naphthylamine bound to whole cells of Escherichia coli. It has been shown elsewhere that this fluorescence increase correlates well with de-energization. Addition of glucose causes a large cyanide-sensitive decrease of intensity, tentatively associated with energization, with the emission spectrum almost returning to the original trace with a peak at 417 nm. These data suggest that there may be a measurable competition between de-energization and energization of the cell membrane, and that the probe fluorescence intensity may be a general indicator of membrane energy level.

The conclusions reached about cellular energy level from measurements of the probe fluorescence intensity correlate partly (a, b below, not c) with the energy level assayed physiologically through rates of active transport: (a) FCCP is found to be a poor inhibitor of proline transport if cells are first incubated with glucose, showing either competition between the processes of energization and de-energization or an increase in the envelope permeability barrier to FCCP caused by glucose addition. (b) Cyanide blocks the fluorescence decrease caused by glucose and inhibits proline and serine transport, consistent with the decrease in probe fluorescence intensity indicating an increase in membrane energization. However, (c) it appears that the amplitude of the fluorescence intensity decrease caused by glucose addition in the presence of FCCP and colicin E1 greatly exaggerates the extent of real membrane energization. Glucose added after uncoupler can cause only a small increase, and after colicin, a negligible increase in the proline transport rate, indicating that the magnitude of the fluorescence intensity decrease after glucose addition is not a true measure of membrane energization, but rather seems to amplify this energization greatly. Glucose addition does not cause a decrease in fluorescence intensity in cells treated with EDTA to remove lipopolysaccharide and an apparent barrier to the probe.

The rotational relaxation time of the probe in intact cells appears to correlate somewhat better with the cellular energy level than does intensity.     

Quantitative fluorescence spectrophotometry of acridine orange-stained unfixed cells. Potential for automated detection of human uterine cancer.

After staining with acridine orange (AO), the nuclei of unfixed cells from the human female genital tract exhibited the same fluorescence behavior previously observed for human and murine leukocytes and mouse ascites tumor cells. With staining conditions chosen to assure saturation of the green-fluorescing AO-nucleic acid complex in normal cells, corrected fluorescence emission spectra were recorded from the entire nucleus of 341 cells taken from 32 normal and 28 abnormal patients. Intensity of the recorded spectra was expressed in phosphor particle units, a fixed arbitrary unit of fluorescence intensity, to display intensity differences among the spectra from the various cell types. In all abnormal samples, one or more cells were found with 530-nm nuclear fluorescence intensity considerably greater than the maximum intensity recorded from normal cells. Determination of the adequacy of 530-nm nuclear fluorescence intensity as a criterion for cancer detection requires additional investigation. Additional criteria, if needed, may be supplied by the metachromasy of AO-stained unfixed cells.     

Effect of magnesium and calcium ions on photoinduced lipid peroxidation and thylakoid breakdown of cell-free chloroplasts

Aging of cell-free chloroplasts at pH 7.0 and 9.0 causes a decline in the level of photosynthetic pigments, quenching of chlorophyll a fluorescence and enhancement in fluorescence polarization. These changes are correlated with photoinduced enhancement of thylakoid lipid peroxidation. The alkaline earth metal cations, namely magnesium and calcium, show opposite actions on lipid peroxidation and modulate thylakoid disorganisation differently. Magnesium ion may stabilise thylakoid membrane by retarding lipid peroxidation. It lowers aging-induced quenching of fluorescence intensity and enhancement of fluorescence polarization. Calcium ion, on the other hand, stimulates disorganisation of thylakoid membranes. It enhances membrane lipid peroxidation, quenching of chlorophyll a fluorescence intensity and fluorescence polarization.     

Tolrestat对高糖所致肾小球系膜细胞肌动蛋白去组装的影响

研究了醛糖还原酶抑制剂Tolrestat对高浓度葡萄糖(HG)所致肾小球系膜细胞(MC)肌动蛋白(actin)组装的影响。结果证明,与正常浓度葡萄糖(NG)相比,在HG培养的MC,F-actin失去束状外观呈不规则网状,显示F-actin部分去组装;F-actin荧光强度降低,G-actin荧光强度升高和F-/G-actin荧光强度比值下降。Tolrestat加入培养后,明显防止HG引起的F-actin去组装及F-和G-actin荧光强度的变化。提示多元醇通路激活在HG引起的MCactin去组装改变中起一定作用。     

Increase in acridine orange (AO) fluorescence intensity of monocytes cultured in plastic tissue culture plates as measured by flow cytometry.

Although the green-red fluorescence of AO is an accepted measure of DNA-RNA content, respectively, it is actually a measure of the fluorescence of dye bound to nucleic acids, and may vary with changes in accessibility to the dye. It has been shown for example that extraction of nuclear proteins results in a marked increase in DNA stainability. Moreover, in certain cell systems the binding of fluorochromes correlates with structural modifications in chromatin that accompany cell differentiation. We report here that changes in green & red fluorescence intensity also occur in long-term monocyte cultures. The increased red fluorescence intensity observed in cultured monocytes may reflect ribosomal RNA synthesis and the increased green fluorescence enhanced AO accessibility to DNA due to changes in chromatin organization. We compared cultured monocytes from bladder cancer patients and healthy donors. The results indicate a small but statistically significantly greater increase in mean green & red fluorescence of cultured monocytes from the cancer patients. These fluorescence variations may indicate differences in the immunologic status of cancer patients and/or be related to disease state.     

Semi-quantitative estimation of changes in noradrenaline content and intraneuronal distribution in the rat vas deferens by fluorescence histochemistry

Summary A semi-quantitative histochemical assay for noradrenaline was developed, based on the assumption that the rate of reaction of noradrenaline with paraformaldehyde depends on transmitter concentration. Changes in organ noradrenaline content caused by drugs or cold-stress were associated with similar changes in fluorescence intensity of organ samples taken for microscopy. Differences in the fluorescence intensity of experimental and control tissues were also found when there was no change in total noradrenaline content, suggesting that fluorescence intensity is not a simple function of whole organ noradrenaline content. Changes in the relative fluorescence of experimental tissues with different paraformaldehyde exposures suggested that the intraneuronal distribution of noradrenaline may affect the rate of development of fluorescence. Analysis of the time course of the fluorescence reaction showed that this was best described by the sum of two first-order exponential components of different half-life. Further results suggested that the first, fast component represents vesicle-bound noradrenaline, while the slow component represents extragranular transmitter.