Twenty years of numerical syntaxonomy

The development of numerical syntaxonomy during its first 20 yr is reviewed. The use of methods of numerical classification and ordination is the dominating feature of the development. National and local phytosociological data banks were established, large data sets handled and many important vegetation monographs were methodically based on multivariate data analysis. Particularly the development in Italy, the Netherlands, Czechoslovakia, and Sweden contributed to new theoretical elements of numerical syntaxonomy. Ordination became a common tool of searching for reticulate synsystematic relations between community types. The most popular ordination techniques have been Principal Components Analysis and Detrended Correspondence Analysis. Hierarchical agglomerative techniques of clustering still prevail in classification, although the divisive strategy of TWINSPAN has also become an effective tool for phytosociological clustering and table sorting. Extensive program packages, also for personal computers have now become standard equipment for many vegetation scientists.     

Effects of detrending and rescaling on correspondence analysis: solution stability and accuracy

Detrending and non-linear axis rescaling potentially improve the accuracy of gradient recovery in correspondence analyses but also reduce the stability or consistency of solutions. Variation among bootstrapped ordination solutions was compared across methods in analyses of both field and simulated data. Solution accuracy, measured with mean squared errors from Procrustes analysis, was compared using simulated data with known structure.Standard detrending-by-segments combined with non-linear rescaling entailed some cost in solution stability, but could improve the accuracy of solutions for long gradients. Without non-linear rescaling these solutions were usually less stable and less accurate. Although detrending-by-polynomials might be preferable on other grounds, it did not produce more accurate or stable solutions than detrending-by-segments.Abbreviations CA = correspondence analysis - DCA = detrended correspondence analysis - MSE = Procrustes mean squared error statistic - SD = standard deviation units of species turnover - SRV = scaled variance in species ranks     

Analysis of variations of handling-time inTrichogramma maidis

Variation in handling-time is studied in the association betweenTrichogramma maidis Pintureau & Vœgelé [Hym.: Trichogrammatidae] and one of its factitious hosts: the eggs of the Mediterranean flour mothEphestia kuehniella Zeller [Lep.: Pyralidae]. It is shown that the duration of egg laying behaviour decreases exponentially from the first host egg encountered onwards. This decreasing kinetic, which corresponds to a learning ability, shows a high variability between females, but a mother-daughter regression analysis fails to demonstrate any genetic transmissibility of this learning ability over 2 successive generations. Once the learning is over, there remains a residual variability which is, in part, under genetic control. The possible consequences of these results on the stability of host-parasite associations are discussed.      

Effects of Solar Radiation on Photoorientation,Motility and Pigmentation in a Freshwater Cryptomonas

The effects of solar radiation on motility, photoorientation and pigmentation have been studied in a freshwater Cryptomonas species. The diaphototactic orientation performed by the cells is impaired within about 90 min of solar radiation. Likewise, the percentage of motile cells within the population and the average velocity of the swimming cells decreases within about the same exposure time. This effect is not due to a thermal stress but rather seems to be caused by the solar UV-B component, since decreasing short wavelength UV radiation by means of an artificial ozone filter or UV cut-off filters increased the tolerated exposure time. Solar radiation also bleached the photosynthetic pigments of the cells as shown by absorption difference spectra.     

Principles and applications of luminescence spectrometry coupled to liquid chromatographic techniques

An overview is presented of the physicochemical basis of luminescence, and its application to the detection of chemicals (drugs, biomedically important compounds, environmentally active substances) in liquid chromatographic systems.     

水稻、小麦、油菜和烟草细胞质雄性不育系统中组分Ⅰ蛋白的比较分析

组分Ⅰ蛋白(RuBP羧化酶/加氧酶)的生物合成系由叶绿体基因和细胞核基因共同控制,所以,被作为研究细胞质遗传的标记。本实验用免疫化学和氨基酸成分分析等方法,对水稻(珍汕97)、小麦(繁7)、油菜(湘矮早)和烟草(G28)的细胞质雄性不育系及其保持系的组分Ⅰ蛋白作了比较,同时对不同作物的组分Ⅰ蛋白也作了免疫鉴定。结果表明,细胞质雄性不育系及其保持系的组分Ⅰ蛋白差异不大,但是,四种不同作物的组分Ⅰ蛋白之间有明显差异。     

小麦再生植株的变异研究 Ⅱ.再生植株当代(R_1代)的细胞学和形态学变异

再生植株具有高频率的染色体异常,其中有20.61％表现为染色体数量变异,最常见的为2n—1类型,其次为2n—2类型,也有2n 1、2n—3个体以及染色体数嵌合株。再生植株减数分裂各期均有染色体异常行为,可以见到的有落后染色体、染色体桥、断片、二分体延迟、微核,还有粗线期十字型配对等结构变异,以及五分体、六分体和畸型四分体等异常现象。微核率随培养时间延长而增加,可用作染色体伤害的一个指标。再生植株R_1代存在着许多形态学变异。性状变异与染色体数目变异没有明显关系。     

Effects of platelet-derived growth factor and fibroblast growth factor on free intracellular calcium and mitogenesis

Although increased free intracellular calcium (Cai) may be one of the main regulators of cell growth and differentiation, studies in cell populations have implied that not all growth factors produce Cai increases. In order to examine in more detail whether Cai increases were related to mitogenesis, we used digital image analysis of intracellular Fura-2 fluorescence to measure Cai in individual BALB/c 3T3 cells stimulated with either platelet-derived growth factor (PDGF) or fibroblast growth factor (FGF). We found that PDGF induced larger and more prolonged Cai increases than FGF did, but that both growth factors induced an initial rapid increase in Cai (less than 2 min) followed by a later sustained increase (greater than 20 min). Only the prolonged Cai increase required extracellular calcium. Following PDGF treatment (1-8 units/ml), the percentage of cells with a large peak Cai increase (greater than twofold) correlated with the percentage of cells made competent (subsequent growth in 1% platelet-poor-plasma). In contrast, purified bovine basic FGF (200-800 pg/ml) and recombinant human acidic FGF (10-300 ng/ml) produced peak Cai increases that were not directly correlated with mitogenesis. In addition, concentrations of intracellular Quin 2 that inhibited Cai transients also inhibited PDGF stimulation but not FGF stimulation of mitogenesis. Thus, Cai increases are necessary for mitogenesis in BALB/c 3T3 cells stimulated by PDGF, but not that stimulated by FGF.     

Image analysis of rat satellite cell proliferation in vitro

Myogenic cells were isolated from adult rat skeletal muscles and cultured in vitro. Cell proliferation was analyzed between days 1 and 14. The cell cycle phases were determined by examining Feulgen-stained cultures with a cell image processor. The nuclei were automatically analyzed by calculating 18 parameters relating to the texture and densitometry of chromatin and the shape of each nucleus. Cell cycle phases were characterized (Moustafa and Brugal, 1984). The recognition methods made it possible to analyse the nuclei of the myogenic cell populations which were either involved in each phase of the mitotic cycle, or left out of the cycle after fusion into myotubes.After 3 hr of culture 10% of the cell population was involved in the cell cycle. In the presence of foetal calf serum, this percentage increased until day 3 after plating. At that time, the DNA content of 28.2% of the cell population was higher than 3C, whereas it is 2C in G1 or G0 nuclei; image analysis showed that 42% of these cells were in S or G2 phase. From day 4, the proliferation rate gradually slowed down until day 8. After day 8, when numerous myotubes differentiated, the percentage of S and G2 phase cells had diminished to between 3 and 8%. The percentage of nuclei in G0 increased when the first myotubes differentiated around day 5. Myotube nuclei were largely in G0. When horse serum was added to the culture medium on day 4 to enhance myotube differentiation, significant cell proliferation was observed before cell fusion.These methods of analysis give the first daily pattern of myogenic cell proliferation and fusion in a cell population isolated from adult muscles.