The ultrastructure of dormant,germinating, and photo-inhibited uredospores of the rust fungusPuccinia graminis f. sp.tritici

Summary A comparison was made of fixed and non-fixed uredospores of the wheat stem rust fungusPuccinia graminis f. sp.tritici, using thin sectioning and freeze-etching. The latter technique yielded new information on the ultrastructure of dormant, germinating, and photo-inhibited uredospores, although the distribution of intramembranous particles (IMPs) was similar in each case. A stereological analysis of thin sectioned specimens provided quantitative data on organelle volumetric densities complementing the qualitative information. Evidence suggests that light acts by preventing the dissolution of wall material in the germ pore regions. Methylcis-ferulate, the uredospore self-inhibitor, is also believed to act at this stage in the germination process, and possible links between photo-inhibition and self-inhibition are discussed.     

Confocal scanning optical microscopy and three-dimensional imaging

Summary— Confocal scanning optical microscopy has significant advantages over conventional fluorescence microscopy: it rejects the out-of-locus light and provides a greater resolution than the wide-field microscope. In laser scanning optical microscopy, the specimen is scanned by a diffraction-limited spot of laser light and the fluorescence emission (or the reflected light) is focused onto a photodetector. The imaged point is then digitized, stored into the memory of a computer and displayed at the appropriate spatial position on a graphic device as a part of a two-dimensional image. Thus, confocal scanning optical microscopy allows accurate non-invasive optical sectioning and further three-dimensional reconstruction of biological specimens. Here we review the recent technological aspects of the principles and uses of the confocal microscope, and we introduce the different methods of three-dimensional imaging.     

The last few milliseconds in the life of a secretory granule

We have monitored single vesicles (granules) in bovine adrenal chromaffin cells using an optical sectioning technique, total internal reflection fluorescence microscopy (TIRFM). With TIR, fluorescence excitation is limited to an optical slice near a glass/water interface. In cells located at the interface, granules loaded with fluorescent dye can be visualized near to or docked at the plasma membrane. Here we give evidence that (1) TIRFM resolves single vesicles and (2) the fluorescence signal originates from vesicles of roughly 350 nm diameter, presumably large dense core vesicles (LDCVs). (3) Diffusional spread of released vesicle contents can be resolved and serves as a convenient criterion for a fusion event. (4) We give details on vesicle properties in resting cells, such as lateral mobility of chromaffin granules, number density, and frequency of spontaneous fusion or withdrawal into the cytoplasm. (5) Upon stimulation with high extracellular potassium, TIRFM reports depletion of the `visible pool' of vesicles closest to the plasma membrane within hundreds of milliseconds, consistent with previous concepts of a release-ready pool. We conclude that TIRFM constitutes an independent assay for pool depletion. TIRFM will allow us to study aspects of secretion that have previously been inaccessible in living cells, in particular the spatial relations and dynamics of vesicles prior to and during exocytosis and re-supply of the near-membrane pool of vesicles. Received: 26 June 1997 / Accepted: 26 September 1997     

水稻成熟花药和花粉的结构和组织化学研究

用乙二醇甲基丙烯酸脂(简称GMA)和环氧树脂Epon812包埋的薄切片方法对水稻成熟花药和花粉的结构进行了观察,并对各种结构的性质和细胞中的后含物做了细胞化学的分析.对成熟花药的绒毡层膜及乌氏体的研究采用了分离技术,做了显微和超微观察.证明水稻成熟花药壁和花粉除具一般禾本科植物特征外,还揭示了花药壁表皮上可能有硅质,药壁表皮细胞内含有脂类颗粒,药室内壁具纤维素质的纤维状加厚;发现花粉粒中除了贮存有大量淀粉颗粒外,还含有脂类,成熟花粉中营养核与两个精细胞及两个精细胞间联系紧密;并讨论了薄切片的优越性,绒毡层膜的意义及其上细胞印迹的来源.     

粗茎鳞毛蕨原叶体细胞有丝分裂过程中微管列阵的变化

应用Steedman‘s wax切片法,间接免疫荧光标记技术和激光共聚焦扫描显微镜技术研究了粗茎鳞毛蕨（Dryopteris crassirhizoma Nakai)原叶体大液泡化细胞和分生组织细胞有丝分裂过程中微管列阵的变化。结果显示：应用高浓度的多聚甲醛（8%）可以很好地保持大液泡化细胞的结构和微管的抗原性。结果也显示Steedman‘s wax切片法和间接免疫荧光标记技术的优点;（1）避免在微管标记过程中酶解细胞壁;（2）在乙醇脱水过程中样品中叶绿素的自发荧光被减到最小;（3）能够详细观察到有丝分裂过程中微管骨架的变化。因此,这种方法可以被广泛用来调查简单植物体和复杂植物体中细胞的有丝分裂过程以及发育过程中微管骨架的变化。     

Raising the speed limits for 4D fluorescence microscopy

Three-dimensional time-lapse (4D) fluorescence microscopy is becoming a routine experimental tool. This article summarizes current technologies, and describes a new method for speeding image acquisition during 4D confocal microscopy.     

IncrementR: Analysing height growth of trees and shrubs in R

Dendrochronology mostly deals with secondary (radial) growth and attention to primary (height) growth has so far been limited. However, tree-ring widths might not adequately represent stem volume increments, net primary productivity and the size of the tree stem carbon sink. The main reason for the prevailing focus on radial growth is that establishing height growth chronologies requires time-consuming and destructive methods. However, for certain ecological applications, less laboriously acquired data on height growth averaged over several successive years are satisfactory. Here we present an R package that contains a set of tools for the analysis of height growth. The tools have been developed for input data of tree-ring widths extracted from series of successive stem height levels. Tree-ring widths ideally represent four directions in each cross section to capture potential changes in stem eccentricity between various height levels. The main computed parameters provided by the package include height growth along the stem, changes of stem eccentricity and stem taper. Accurate determination of average height growth depends on the correct estimation of the number of tree rings at different stem height levels, which might be complicated by missing rings in off-pith cores. The presented package therefore also contains functions implementing common procedures for the estimation of the number of missing tree rings near to the pith. Most outputs can be visualized graphically. The package is useful for estimating height growth in ecological and dendrogeomorphological studies, especially in situations where both primary and secondary growth is influenced by different environmental factors. It is also useful for analysing tree-ring chronologies assembled using serial sectioning, which typically applies to shrubs.     

Optical sectioning and high resolution visualization of trabecular meshwork using Bessel beam assisted light sheet fluorescence microscopy

Glaucoma, one of the leading causes of blindness, is an eye disease caused by irregularities in the ocular aqueous outflow system causing an elevated intraocular pressure. High resolution imaging of the aqueous outflow system comprising trabecular meshwork is immensely valuable to vision analysts and clinicians in comprehending the disease state for the efficacious analysis and treatment of glaucoma. Currently available ocular imaging devices are unable to deliver high resolution images for the visualization of the trabecular meshwork. A method to obtain high resolution (sub‐micrometer) images of the trabecular meshwork using Bessel‐Gauss beam scanned light sheet fluorescence microscopy is presented and the optical sectioning capability of this technique to obtain three‐dimensional volumetric images of the trabecular meshwork of an intact eye without any physical dissection is demonstrated. Figure: Three‐dimensional visualization of trabecular meshwork of porcine eye.      

A novel tight cylindrical mold for epoxy resin embedding allows enhanced microscopic analysis of microcores extracted from woody plants

A novel mold was devised to embed microcores extracted from stems of trees in epoxy resin, which has been widely used for optical and electron microscopic analysis of xylem formation. The embedding mold of a tight cylindrical shaped tube was designed to avoid displacement of microcores from the right position during the process of resin embedding. Microcores of a ring-porous hardwood species, Quercus crispula, with higher wood density and much larger differentiating vessel elements laid down on the boundary between the current xylem and the previous one, which generally cause difficulty in thin sectioning and breaks in sections, respectively, were embedded in the cylindrical molds full of epoxy resin. Locations of the three principal planes of wood anatomy could be determined in cylindrical resin-embedded microcores as follows: the transverse plane could be found on their side of cylinder, the radial one was vertical to the transverse, and the tangential ones were their circular ends of cylinder. The present embedding mold, therefore, can provide all three principal sections for microscopic wood anatomy from the side or ends of the same cylindrical microcore in principle. To confirm the usefulness of the resin-embedded microcores, we examined the differentiation of vessel elements during the period of earlywood formation on their transverse sections under microscopes, consequently could observe cell division in the cambial zone and sequential stages of vessel element differentiation, including cell expansion and deposition of the secondary cell wall. The present embedding mold for epoxy resin is simple but highly useful and innovative for a wide range of applications of microcores in microscopy for studies on tree-ring formation.