Staining Tomato Fruit Cuticle and Exocarp Tissues

Immature fruit of tomato, Lycopersicon esculentum (Celebrity), was examined to observe the cuticle, its interface with the epidermis, and the general histology of the outer exocarp. Paraffin sections were stained first with Bismarck brown Y. Structures already stained in various hues of brown were stained again with either azure B, aluminum hematoxylin and alcian blue 8GX, or the periodic acid-Schiff (PAS) reaction. Bismarck brown-azure B displayed the cuticle in strong contrast with subjacent tissue; however, nuclei were not easily identified at low magnification. Bismarck brown-hematoxylinalcian blue produced a sharply contrasted combination of yellow cuticle, bright blue cell walls and purple nuclei. Nuclei stained purple with hematoxylin were easily identified at × 100. Bismarck brown-PAS stained the cuticle golden brown and subjacent tissues magenta red. Surprisingly, epidermal cells stained specifically and intensely with PAS while pretreatment with an aldehyde blockade and omission of periodic acid prevented staining of all other tissues.     

Iodine as an Aid in Identification of Asci and Ascospores of Schizosaccharomyces octosporus

Transverse paraffin sections of mature greenwood stems of rose (Rosa x hybrida) and flowering dogwood (Cornus florida L.) were stained with Bismarck brown followed by azure B or tolnidine blue O. The Bismarck brown was replaced by thiazin dye metachromasia in all structures except the cuticle which remained brown or yellow. The interface between the cuticle and exterior cell walls of the epidermis was delineated clearly.     

Oil Blue N or Na as a Fat Stain for Animal Histology

Oil blue N or NA gives precise dark blue staining of fatty substances in animal tissues when supersaturated solutions in dilute isopropanol are used. A stock saturated solution in 60% isopropanol, when diluted to 40 or 50% isopropanol, gives good staining in 5 to 10 minutes, without appreciable precipitate.

Suitable counterstains are 1:1000 solutions of Janus green B, Bismarck brown Y and Bismarck brown R. These require about 5 minutes and should be followed by one-minute differentiation in 5% acetic acid. Of the three, Bismarck brown R gives the best contrast.     

The Use of Bismarck Brown Y in some new Stain Schedules

The staining quality of Bismarck brown Y may be improved and sterility maintained by adding 5% phenol to a 1% aqueous solution. Use the phenolic Bismarck brown in combination with iron alum hematoxylin except for stripped epidermis in the following procedures:

Stem and Root Schedule: Mordant sections from water in 4% iron alum for 10 minutes. Rinse in distilled water and stain in 0.5% aqueous hematoxylin for 1 minute or until darkly stained. Rinse in distilled water and destain in 2% iron alum until a gray color appears. Rinse thoroly in distilled water and intensify hematoxylin by transferring sections to 0.5% aqueous lithium carbonate until the desired black color appears. Rinse thoroly in distilled water and stain for 1-5 minutes in phenolic Bismarck brown. Rinse in distilled water, dehydrate successively in 30, 50, 70, 95 and 100% alcohol. Clear in methyl salicylate for 5 minutes, then to xylene for 3-5 minutes, and mount in balsam.

Middle Lamellae in Wood: Destain more thoroly in 2% iron alum than for the general stem and root schedule, and intensify in lithium carbonate for a longer period (about 1 hour).

White Potato Tuber Sections: Modify above schedule by reducing time of destaining in 2% iron alum to about 30-60 seconds and intensify hematoxylin until starch grains appear bluish in color. Stain in phenolic Bismarck brown for 1-2 minutes.

Wheat Grain Sections: Fix grain for sectioning when in “dough” stage. Use schedule the same as for potato tuber except for reducing time of staining in phenolic Bismarck brown to about 45 seconds.

Tradescantia zebrina Epidermis: Strip epidermis from leaf while submerged in water. Fix in 100% alcohol 10 minutes, pass thru 95, 70, 50, 30, and 10% alcohol to water. Stain in phenolic Bismarck brown for 10-20 minutes. Dehydrate, clear in methyl salicylate and mount in balsam.     

Staining of plant Materials Cleared in NaOH

Stains are listed which have proved suitable for staining the epidermis, mesophyll, and sclerenchyma and tracheary elements, respectively, of cleared leaf material of Mouriri and Linociera. Too rapid leaching is avoided by overstaining high in the dehydration series, destaining briefly in the same solvent, and moving through to xylene. Twenty to thirty minutes staining time is generally sufficient. Concentrations and solvents can be varied widely. If destained too much, the material can usually be replaced in the dye with no ill effects. A double stain schedule (Bonnett) of five to ten minutes in 1% Bismarck brown Y in 95% alcohol followed by one to two minutes in 1% fast green FCF in 100% alcohol may be advantageous for thin-walled cells in thick material. It may be preferable to treat thinner material with tannic-acid-iron-chloride followed by safranin (Foster). The effects of bleaches and clearing compounds other than NaOH on staining have not been investigated; however, Dr. Bonnett finds that lactic acid used after NaOH improves clearing and also improves the staining of his combination (above). Mordants can doubtless be used to advantage.     

松属针叶角质层微形态特征在分类学中的应用

角质层是表皮细胞壁表面的一层不透水的脂肪性物质。角质层与表皮细胞紧密结合,植物表皮细胞形态和排列方式、气孔器的形态结构等微形态特征均能在角质层上反映出来。利用光学显微镜和扫描电镜对松属（Pinus）12种植物针叶角质层微形态特征进行观察和比较,详细描述20个性状,其中12个性状来自角质层内表面,8个性状来自角质层外表面。结果表明,这些特征可为该属属下分类和相似种的鉴别提供有用信息,具有重要的分类学意义：①表皮细胞长度、表皮毛长度、角质层外表面起伏程度、表皮细胞轮廓、有无气孔塞和针絮状物质等角质层微形态特征具有自身特异性,在属下可作为松属组级水平上的分类依据。角质层微形态 特征不支持将五针松组（P. Section Cembra）和白皮松组（P. Section Parrya）合并为P. Section Quinquefolius的观点,亦不支持将油松组（P. Section Pinus）分成P. Section Pinus和P. Section Trifolius的看法。②白皮松（P. bungeana）针叶角质层微形态特征既与五针松组有相同之处,又与油松组有相似之处,还有部分特征显示出不同于松属其他种类的独特性,可为白皮松亚属（P. Subgenus Parrya）的建立提供新依据。③扫描电镜下表皮细胞垂周壁纹路,气孔塞有无和外表面气孔形状等特征可为形态相似种火炬松（P. taeda）和湿地松（P. elliottii）提供种间界定依据。     

Bismarck Brown As A Stain For Mucoproteins

Bismarck brown has been used for many years as a stain for mucin. But some types of mucoprotein are so water-labile that they cannot be demonstrated by the aqueous or weak alcoholic solutions usually employed. It has been found that Bismarck brown in slightly acidified, strong alcoholic, solution stains mucin. A simple method is given for using this solution for staining water-stable mucoproteins. Another method is included in which full precautions are given for avoidance of water at all stages subsequent to fixation. This method must be used for the more water-labile mucoproteins. By the use of these methods, it has been possible to demonstrate a wide range of mucoproteins including those of the mast cells of Hardie and that of the zona pellucida of the graafian follicle.     

中国罗汉松属叶角质层微形态结构及其分类意义

利用扫描电镜对罗汉松属8种2变种植物叶角质层内外表面进行了细致观察。发现罗汉松属植物叶角质层结构具有许多相似特征,表皮细胞较为规则,长方形或多边形,边缘波状弯曲;气孔器排列成带状,长轴均与叶脉一致,气孔器具较为明显的气孔塞和伏罗林环,气孔器保卫细胞极延伸明显,通常具有2~4个副卫细胞、不具极副卫细胞。但罗汉松属叶角质层结构也具有明显的种间差异,镰叶罗汉松和洛杉矶罗汉松同其它种类差异最大,这两种植物叶两面均具气孔器,角质层内表面垂周壁直,角质层凸缘不明显;贺氏罗汉松最为显著的特征是近轴面和远轴面表皮细胞的垂周壁角质层厚且凸缘均极其发达;小叶罗汉松近轴面表皮细胞排列较为规则,多数为方形,长轴与叶脉垂直,垂周壁之间的角质层突起较为显著,延伸到皮下层;兰屿罗汉松近轴面表皮细胞排列较不规则,多边形,细胞的角端比较钝,没有棱角;大理罗汉松气孔带间隔较小,有时两条气孔带挤在一起,使副卫细胞紧连,近轴面表皮细胞较短,方形或长方形,垂周壁之间的角质层较不发达;海南罗汉松角质层气孔带间隔较宽,气孔器形状为阔椭圆形,近轴面表皮细胞均为细长方形;变种短叶罗汉松和狭叶罗汉松与罗汉松也具有明显差异,短叶罗汉松近轴面表皮细胞排列不规则,垂周壁深波状弯曲,凸缘极为明显,但原种罗汉松近轴面表皮细胞排列较为规则,垂周壁浅波状弯曲,凸缘不明显,而狭叶罗汉松近轴面表皮细胞方形或长方形,比罗汉松的表皮细胞短,垂周壁直或略弯曲,角质层极厚。这些角质层微形态特征差异可以作为罗汉松属内种类分类鉴定的依据。     

Characterization of tyrosine hydroxylase from Manduca sexta

In insects, 3,4-dihydroxyphenylalanine (DOPA) is required for tanning of newly formed cuticle and the production of melanin during some types of immune responses. DOPA is produced by the hydroxylation of tyrosine, and this reaction can be catalyzed by two types of enzymes: tyrosine hydroxylase (TH) and phenoloxidase (PO). TH is required for cuticle tanning in Drosophila melanogaster and for cuticle pigmentation in other insect species, but additional functions of TH have been uncertain. In contrast, an immune function for PO has been well documented. The goal of this study was to characterize TH from Manduca sexta with a focus on its possible contribution to cuticle tanning and immune-associated melanization. We cloned a full-length TH cDNA, purified recombinant TH, and confirmed that MsTH and MsPO have tyrosine hydroxylating activity. To determine possible functions, we analyzed TH expression profiles. TH mRNA and protein were present in eggs at the stage when the pharate larval cuticle begins to tan and also in the integument of molting larvae. The amount of TH in the integument was correlated with the degree of cuticle tanning. Unlike PO, which was found to be constitutively expressed by hemocytes and was present in plasma, TH was upregulated in hemocytes and the fat body in response to an immune challenge and remained intracellular. These data suggest that TH is required for cuticle tanning and immunity in M. sexta. Based on the collective information from many studies, we propose a model in which TH is a major producer of the DOPA required for both cuticle tanning and immune-associated melanization.     

Inter- and intra-specific cuticle variation between amphimictic and parthenogenetic species of root-knot nematode (Meloidogyne spp.) as revealed by a bacterial parasite (Pasteuria penetrans)

Specific host–parasite interactions exist between species and strains of plant parasitic root-knot nematodes and the Gram-positive bacterial hyperparasite Pasteuria penetrans. This bacterium produces endospores that adhere to the cuticle of migrating juveniles, germinate and colonise the developing female within roots. Endospore attachment of P. penetrans populations to second-stage juveniles of the root-knot nematode species Meloidogyne incognita and Meloidogyne hapla showed there were interactive differences between bacterial populations and nematode species. Infected females of M. incognita produced a few progeny which were used to establish two nematode lines from single infective juveniles encumbered with either three or 26 endospores. Single juvenile descent lines of each nematode species were produced to test whether cuticle variation was greater within M. hapla lines that reproduce by facultative meiotic parthenogenesis than within lines of M. incognita, which reproduces by obligate parthenogenesis. Assays revealed variability between broods of individual females derived from single second-stage juvenile descent lines of both M. incognita and M. hapla suggesting that progeny derived from a single individual can differ in spore adhesion in both sexual and asexual nematode species. These results suggest that special mechanisms that produced these functional differences in the cuticle surface may have evolved in both sexually and asexually reproducing nematodes as a strategy to circumvent infection by this specialised hyperparasite.     

Hornet cuticle: effects of short-term UV irradiation

Effects of short-term UV irradiation were investigated on various cuticular parts of workers and queens of the Oriental hornet, to wit: brown strip, yellow strip and wing. On each preparation of the afore-mentioned, a reading of the relative optical density (ROD) was taken prior to, immediately following, and 15-30 minutes after its irradiation as compared to white light irradiation. The results showed that brief UV irradiation causes changes in the ROD of hornet cuticle, and that these changes in ROD are different in brown than in yellow cuticle. Those in yellow strip are induced by the presence or absence of the active yellow pigment, whose quantity in worker cuticle is different than in queen cuticle, probably due to the various activities in which they are involved during the active season.     

Distribution of cuticular protein mRNAs in silk moth integument and imaginal discs

The distributions of mRNAs for two cuticular proteins of Hyalophora cecropia were examined with RT-PCR and in situ hybridization. For major regions of larval and pupal cuticle, there was a strong correspondence between the type of cuticle and the predominant cuticular protein message found. Epidermal cells underlying soft cuticle had mRNA for HCCP12, with a RR-1 consensus attributed to soft cuticle, while the epidermal cells associated with hard cuticle had predominantly mRNA for HCCP66, a protein with the RR-2 consensus attributed to hard cuticle. Both messages were found in all areas of the pupal fore- and hind-wings, with modest area-specific difference in concentration being much less than differences in the relative abundance of these cuticular proteins.

mRNA for HCCP12 was present in imaginal discs of feeding larvae of H cecropia. Data from Bombyx mori available at SilkBase (http://www.ab.a.u-tokyo.ac.jp/silkbase/) revealed that imaginal discs from feeding larvae had abundant mRNA for RR-1 cuticular proteins, representing six distinct gene products. Only discs from spinning larvae had mRNAs that coded for RR-2 proteins arising from 10 distinct genes. Thus, lepidopteran wing imaginal discs can no longer be regarded as inactive in larval cuticle production.     

The thermo-photoelectric (TPE) properties of the hornet cuticle: correlation with the morphological structure

The present study investigated thermoelectric phenomena in the cuticle of the Oriental hornet Vespa orientalis (Hymenoptera, Vespinae). This was done in dependence on the pigment extant at various cuticular region, that is, the brown cuticle in which the primary pigment is melanin and embedded within the cuticle, and the yellow stripes in which the yellow pigment is comprised of purines and pteridines that are located in special pockets between the upper part of the cuticle and the basement membrane. The yellow pigment could be separated from the cuticle proper, but the brown pigment was not thus separable. We found that all cuticular regions of the gaster evinced a thermoelectric response, in that with rise in temperature there was a rise in the thermoelectric current, and vice versa. Additionally, the intact hornet displayed a negative photoelectric response in each of its yellow segments, so that upon illumination with UV light, the maximal current dropped by about 40-50%. Measurements taken on individual stripes in the gaster segments revealed that the photoelectric response is elicited only in the yellow stripes. In all the latter the photoelectric response persists but the maximal current level is lower than in the intact whole hornet. If the yellow pigment is detached mechanically or by bacterial incubation, the photoelectric property of the cuticle is abrogated. Likewise the photoelectric property is abrogated upon immersion of the cuticle in alcohol, even though the yellow pigment is still retained. The specific heat of the yellow stripes in the cuticle is about twice as high as that of the same stripes that had been depleted of their yellow pigment, amounting to 1.8-1.9 J/g.K vs. 0.8 J/g.K.     

Multiple Staining of Isopropanol Prepared Tissues with Phloxine B and Bismarck Brown Y

Two methods employing phioxine B and Bismarck brown Y followingdehydration and infiltration using a graded series of isopropylalcohol-paraffin combinations are presented: (1) a five-componentstain combination for highly differentiated plant tissues inwhich orange G is included to differentiate between the otherdyes and (2) a triple stain combination especially useful forgeneral differentiation. Both methods are uniformly successfuland result in colour-fast sections. Advantages of the isopropylalcohol technique are: diminished distortion and less hardeningof the material, ready availability, and low cost. Brief detailsof some of the stains used and their advantages are discussed. Phloxine B, organge G, Bismarck brown Y, isopropanol, Metasequoia glyptostroboides, dawn redwood, Polystichum tsus-Simense, Holly fern, histology     

我国主栽食用菌茶薪菇的物种概念

茶薪菇是我国广泛栽培的一种食药用菌,由于其形态特征与柱状环伞十分相似,分类地位至今尚不明确.本研究采用形态学和多基因分子系统发育分析相结合的方法,研究茶薪菇和柱状环伞的分类问题,结果表明:茶薪菇和柱状环伞是两个不同但亲缘关系密切的物种;在形态上,茶薪菇菌盖颜色浅褐色至深褐色,油茶味浓,菌环较薄易脱落,褶缘囊状体柱状、烧...     

Additional Schiff-Type Reagents for Use in Cytochemistry

Twenty-four new Schiff-type reagents were discovered in a survey of 140 different dyes. These dyes include acid fuchsin, acridine yellow, acriflavine hydrochloride, azure C., Bismarck brown R, Bismarck brown Y, celestine blue B, chrysoidine 3R, chrysoidine Y extra, cresyl violet, crystal violet, gentian violet, methylene blue, neutral violet, phenosafranin, phosphine GN, proflavine, toluidine blue O, and toluylene blue. Positive results obtained with crystal violet and a few samples of methylene blue are considered due to impurities. Various chemical extractions, aldehyde blocking reagents, and enzymatic treatments were used to verify the aldehyde specificity of the above dye-SO₂, reagents as well as azure A, brilliant cresyl blue, neutral red, safranin O, and thionin which have been mentioned by other workers. These reagents were tested in the Feulgen reaction for DNA and the PAS reaction for polysaccharides. Absorption curves were obtained from individual nuclei stained for DNA. The absorption peaks ranged from 450 mμ, to 630 mμ. depending on the dye studied. The Feulgen reaction could be followed by the PAS reaction or vice versa in mouse intestine using reactive dyes of complementary colors. The evidence indicates that a potential Schiff-type reagent must have at least one free NH₂ group on the dye molecule.     

Phosphotungstic Acid-Eosin Combined with Hematoxylin as A Stain for Negri Bodies in Paraffin Sections

Experimentation with the Papanicolaou stain in this laboratory led to the discovery that the eosin, combined with phosphotungstic acid, was responsible for differential staining of Negri bodies. Eosin prepared as in EA 36 was used, but without the light green and Bismarck brown. Paraffin sections of hippocampus from brains of animal affected with rabies were fixed in 10% formol or in a mixture of 2 volumes of saturated aqueous HgCl₂ and 1 volume of absolute alcohol. They were stained first with hematoxylin and then with eosin. This procedure gave better results than staining with other types of eosin or by the original EA 36 mixture. The Negri bodies were well stained and their structure easily visible. The best results were obtained from material fixed with the HgCl₂ solution.     

Isolation of Cuticle and Vascular Bundles of Leaves by Maceration in Rumen Fluid

We report a new macerating technique for plant leaves which permits the isolation of cuticle and vascular bundles. The maceration medium is rumen fluid, a complex mixture of interacting microorganisms, used full strength or diluted with a nutrient buffer solution in the ratio of 2:5. An incubation period of up to 72 hours at 39 C permits cuticle and vascular-bundle networks to be isolated. The technique is illustrated with fresh leaf samples from pearl millet, Pennisetum typhoides; orchardgrass, Dactylis glomerata; and alfalfa, Medicago sativa.