胶州湾浮游植物水华期群落结构特征

根据2001年8月对胶州湾海域进行的为期2d的大面积调查资料,对浮游植物的群落结构进行了初步研究,结果表明,浮游植物群落主要由沿岸暖水性种类组成,以硅藻为主,共34种;还有少量的甲藻7种和绿藻1种,湾中央水域出现的物种数最多,为37种;湾边缘最少,仅出现10种,细胞数量的密集区出现在湾东部边缘水域,最高值为6．96×10⁸个cell·m^-3;低值区出现在湾口,最低值仅为3．18×10⁶个cell·m^-3调查期间浮游植物的物种多样性及其均匀度的最低值均出现在湾东部边缘水域;高值区出现在湾口和湾中央水域,胶州湾海域水团运动和水体富营养化程度是影响浮游植物群落分布的主要环境因素。     

太湖蓝藻滤液的遗传毒性研究

蓝藻爆发是环境污染引发的重要事件之一,随之产生的蓝藻毒素又直接危及区域水安全.该论文采用蚕豆和大蒜根尖微核试验研究了太湖蓝藻暴发期间蓝藻滤液的遗传毒性.结果表明,同阴性对照相比,所有试验处理对蚕豆根尖细胞微核发生率的影响显著增加;对大蒜根尖细胞微核发生率而言除蓝藻滤液8倍稀释液的影响不显著外,其它水平效应显著高于阴性对照,而且表现出一定的剂量效应.暴发期蓝藻滤液原液对蚕豆根尖细胞微核发生率影响显著高于阳性对照(0.8mg·mL^-1环磷酰胺)的效应,从而说明蓝藻暴发时期蓝藻滤液具有较强的遗传毒性.通过微核试验效果分析,蚕豆作为植物监测系统的敏感性和稳定性都优于大蒜材料.     

Fluorescence characteristics of cyanobacteria (blue-green algae)

The fluorescence characteristics of the cyanobacteria Synechocystisaquatilis Sauv., Microcystis firma (Breb. et Lenorm.) Schmidleand Synechococcus leopoliensis (Racib.) Kom. and the green algaScenedesmus quadricauda (Turp.) Breb. were examined. In thethree cyanobacteria, phycocyanin is the main accessory pigment.Phycoerythrin is not present in our investigated strains ofcyanobacteria. The highest excitation of the chlorophyll a (Chla) fluorescence of cyanobacteria resulted from light with wavelengthsof 620–630 nm. A definite ‘Kautsky’ effectis also evident at this wavelength. However, excitation withblue light (420–520 nm) produced only very slight fluorescence.The Kautsky effect is not evident at these wavelengths, evenat high photon flux densities. For Scenedesmus, fluorescencecharacteristics typical of green algae were found. The fluorescenceexcitation of cyanobacteria at 620 nm corresponds to a photosynthesispeak in the action spectrum measured in terms of O₂ production.The results underline the necessity of fluorescence measurementsat several wavelengths whenever mixed populations are involved.Such measurements also present possibilities for more accurateestimation of biomass and potential photosynthetic productionin mixed populations.     

Mesosomes in blue-green algae

Summary Mesosome-like, unit-membrane structures are clearly defined in the blue-green algae, Spirulina and three strains of Synechococcus, after osmium or potassium permanganate fixation and observation with the electron microscope. The membranous structures are distinct from the photosynthetic membranes and, in the case of Spirulina, are frequently observed in cells and can occur in large volume within the cell.     

Morphology-habitat associations in blue-green algae

Morphological and habitat features have been recorded on punchcards for three genera in the Oscillatoriaceae and two in the Nostocaceae. As a result it is concluded that generic divisions in the Oscillatoriaceae are arbitrary and artificial, but that in the Nostocaceae, Cylindrospermum represents a grouping of distinct forms to a greater degree than does the amorphous genus Anabaena.

Some morphological comparisons between the two groups are attempted and detectable associations between morphological and habitat features are suggested : together these may contribute to an eventual separation of taxa on a more logical basis than at present.     

Nitrogen chlorosis in blue-green algae

Summary Nitrogen deficient Anacystis nidulans contained normal levels of chlorophyll-a and carotenoids but did not contain any phycocyanin. These organisms also contained large amounts of polysaccharide. The addition of nitrate to a deficient culture resulted in the recovery of normal pigmentation over a period of several hours.The relation between these changes and growth was established by a kinetic study of the changes in cell composition during pigment loss and recovery. Loss of phycocyanin commenced with the cessation of growth due to nitrogen limitation and was complete after 15 hours. In contrast there were only minor changes in chlorophyll-a and carotenoid. After growth had ceased polysaccharide continued to increase and viability dropped sharply although total cell counts did not change. These trends were reversed by the addition of nitrate to deficient cultures. Phycocyanin was detected after a short lag and normal levels of phycobiliprotein were present within 8 hours. Cell division did not begin until normal levels of phycocyanin had been restored. During the recovery of normal pigmentation there was a decrease in reducing sugar content and a sharp rise in viability. Qualitative studies with 9 additional blue-green algae suggest that loss of phycocyanin is a characteristic feature of nitrogen deficiency in blue-green algae.     

Relation between pigment content and photosynthetic characteristics in a blue-green algae

1. The blue-green alga Anacystis nidulans was cultured under steady state conditions at 25 and 39°C. and under several different light intensities to give five different types of cells. 2. Cells were submitted to pigment analysis based upon acetone extracts and aqueous extracts obtained by sonic disintegration. The different cell types show a threefold range of chlorophyll content and a fourfold range of phycocyanin content with only minor changes in the chlorophyll/phycocyanin ratio. Cells of highest pigment content were estimated to contain 2.8 per cent chlorophyll a and 24 per cent phycocyanin, the latter on a total chromoproteid basis. 3. Light intensity curves of photosynthesis were obtained for each of the cell types at 25 and at 39°C. The slopes of the light-limited regions of the curves are approximately linear functions of chlorophyll and phycocyanin contents. Maximum light-saturated rates of photosynthesis at 25 and 39° show no simple relation to pigment content.     

The influence of daylength,light intensity and temperature on the growth rates of planktonic blue-green algae

The in vitro growth rates under continuous light of the four dominant blue-green algae in Lough Neagh, Anabaena flos-aquae Bréb., Aphanizomenon flos-aquae Ralfs fa. gracile Lemm., Oscillatoria agardhii Gom. and Oscillatoria redekei van Goor were slower than in situ rates from Lough Neagh that had been corrected for hours of light received by the algae. However, by culturing on a 6: 18 light-dark cycle in vitro growth rates were obtained that were similar to the in situ rates. Under continuous light small species showed the fastest growth with Oscillatoria redekei the dominant species. However, this pattern was almost completely reversed under the light-dark cycle with Oscillatoria redekei only exhibiting the fastest growth rate under low light conditions. This observation showed agreement with Lough Neagh field data which showed that Oscillatoria redekei reached its maximum crop in April while the other three species were dominant during the summer months. Compared to the generally assumed high thermal tendency of blue-green algae the temperature maxima of the four species were low. No growth was observed at 35°C for any species while Anabaena flos-aquae was severely inhibited at 25°C.     

The taxonomy of blue-green algae

The conventions at present used in the classification of blue-green algae frequently prove unsatisfactory. A solution is suggested which requires the simultaneous use of two different approaches. When a binomial is essential the flora of Geitler (1932) should be adequate for most purposes, but any long term attempt to sort out the present chaos will require the use of numerical taxonomy. This dual approach will necessitate various practical changes in current methods of naming and reporting on blue-green algae.     

The carotenoids of blue-green algae

The carotenoid compositions of Phormidium persicinum, P. luridum, P. faveolarum and Anabaena flos-aquae have been studied, both quantitatively and qualitatively. β-Carotene is the major carotenoid in all species. The xanthophylls comprise zeaxanthin, echinenone, canthaxanthin and the furanoid mutatochrome. Phormidium persicinum lacks glycosidic carotenoids. Myxoxanthophyll (myxol-2′-rhamnoside) and a 4-ketomyxol-2′-methylpentoside (tentatively 4-keto-myxoxanthophyll) are present in the other species. These distribution patterns are compared with those observed in other blue-green algae and some correlations with taxonomy are apparent.     

Hydrocarbons in green and blue-green algae

Liquid column chromatography and thin-layer chromatography were used to determine the total content of hydrocarbons and gas chromatography was used to evaluate composition of hydrocarbons in green algae (Chlorella kessleri, C. vulgaris, Chlorella sp.,Scenedesmus acutus, S. acuminatus, S. obliquus) and the blue-green alga (Spirulina platensis) cultivated under autotrophic or heterotrophic conditions. InC. kessleri cultivated under heterotrophic conditions the content of hydrocarbons was found to be about 10^-2 % (per dry mass), whereas under autotrophic conditions it was about 10^-3 % (per dry mass). The highest content of hydrocarbons was detected in species of the genusScenedesmus cultivated autotrophically (10^-1 %). Heptadecane and hexacosane were found as major alkanes, 1-heptadecene was detected among alkenes.     

Heterocyst division in two blue-green algae

Bacteriophage 16-6-12 of Rhizobium lupini has a long, non-contractile tail and a head which is hexagonal in outline. The tail is 140 nm in length, 11 nm in diameter, and carries a short terminal fiber. Analysis of the tail structure by optical diffraction indicates that it is of the helical “stacked disc” type. After phenol-extraction from purified particles, the DNA of phage 16-6-12 can circularize in vitro. No significant difference in contour length was observed between the linear (14.34±0.28 μm) and circular (14.44±0.24 μm) forms of molecules. After partial denaturation with alkali an AT-GC-map was constructed, which shows an asymmetric distribution of AT- and GC-rich regions. It is concluded that this phage DNA can circularize due to the presence of cohesive ends and that it is not circularly permuted.     

The program of protein synthesis during heterocyst differentiation in nitrogen-fixing blue-green algae

The program of protein synthesis that accompanies cellular differentiation following transfer of the blue-green alga Nostoc muscorum from nitrogen-containing to nitrogen-free medium has been determined by polyacrylamide gel electrophoresis of whole cell proteins labeled with ³⁵SO₄⁼ during successive intervals of the differentiation. Differentiating cells (proheterocysts, which become heterocysts) are distinguished from vegetative cells on the basis of the latter's susceptibility to lysis with lysozyme.At least ten sets of proteins can be distinguished on the basis of the time at which they are synthesized or the type of cell in which they are located. Regulation of most of these sets can be accounted for by classical induction or repression involving NH₄⁺ or a simple derivative of NH₄⁺. An additional mechanism is required to explain how the synthesis of several sets of proteins is initiated in all cells following transfer to nitrogen-free medium, but is permitted to continue only in developing proheterocysts. The structural polypeptides of the nitrogenase enzyme complex are members of the latter set.In differentiated filaments, very few proteins are synthesized in both vegetative cells and heterocysts. The qualitatively different pattern of protein synthesis is established very early, within the first 9 hr after transfer. Moreover, the proteins present in proheterocysts at that time are already qualitatively different from those of vegetative cells. Rapid turnover of vegetative cell proteins appears to be a characteristic of the early development of proheterocysts.