A Bodian method for mounted frozen sections.

For application of the Bodian method to frozen sections, cut frozen peripheral nerve or muscle at 10 mum and mount. Fix for 4 days in 18 parts 80% ethanol, 1 part 10% formalin, and 1 part glacial acetic acid. Fix central nervous tissue in the same mixture prior to freezing and sectioning, and after mounting postfix for 4 days. Impregnate by the Bodian procedure. The results equal Bodian stains of paraffin sections. The technique is simple and reliable. The use of 10 mum frozen sections produces little artifact and allows alternate serial sections to be stained with other techniques.     

A Copper Sulfate-Silver Nitrate Method for Nerve Fibers of Planarians

For staining in toto, planarians are fixed in a mixture of 10 ml of commercial formalin, 45 ml of 95% ethanol and 2 ml of glacial acetic acid. After treatment with 70% ethanol 3-10 days, they are washed in distilled water and immersed in 10% CuSO₄. 5H₂O for 3 hr at 50° C, transferred without washing to 1% AgNO₃ for 1.0-1.5 hr at 50° C; and then developed in: 10 ml of 1% pyrogallol, 100 ml of 56% ethanol and 1 ml of 0.2% nitric acid. Gold toning, 5% Na₂S₂O₃ and dehydration follow as usual. For staining sections, material is fixed in the same fixative, embedded in paraffin and sectioned at 10 μ. After bringing sections to water, they are immersed in 20% CuSO₄. 5H₂O for 48 hr at 37° C; then rinsed briefly in distilled water and placed in 7% AgNO₃ for 24 hr at 37° C. They are washed briefly in distilled water and reduced in: hydroquincne, 1 gm; Na₂SO₃, 5 gm and distilled water 100 ml. Gold toning, followed by 5% Na₂S₂O₃ and dehydration completes the process. Any counterstaining may follow.     

Modification of maize starch by thermal processing in glacial acetic acid

Differential scanning calorimetry (DSC) and X-ray diffraction (XRD) methods were used to determine if corn starch–glacial acetic acid mixtures can be melted and thermally processed at reasonable temperatures. DSC studies showed that the melting temperature of dry starch was reduced from about 280 to 180°C in the presence of >30% acetic acid. Glass transition temperatures varied from 110 to 40°C at 15 and 45% acetic acid, respectively. XRD showed the loss of native starch crystallinity and the formation of V-type complexes. Addition of 10% water decreased the melting temperatures to 140–150°C while addition of a base (sodium acetate) had little effect. Some possible applications of processing starch in glacial acetic acid will be discussed.     

A Celloidin Infiltration-Frozen Section Sequence for Enhanced Preservation of Phosphatases in Bone

The effect of the following embedding procedures on the acid and alkaline phosphatase content of decalcified mouse tibiae has been studied: embedding in 23% gelatine for 18 hr at 37° C, embedding in paraffin wax in vacuo for 1 hr at 58° C, and impregnation with 4% celloidin in diethyl ether and ethanol at 4° C for 2-3 days. Unsupported tissues were also used to demonstrate these enzymes for comparison with the above procedures. Tibiae were first fixed in 10% neutral formalin at 4° C for 15 hr, decalcified in equal volumes of 2% formic acid and 20% sodium citrate at pH 4.9 for not more than 5 days and then washed in distilled water before carrying out the embedding schedules. The celloidin-impregnated tibiae were placed in 70% ethanol to harden the celloidin and then washed in distilled water for 1-2 hr. These tibiae and those embedded in gelatine were cast in a gelatine block which was then hardened in 10% neutral formalin at 4° C for 2 hr. Sections of these and unsupported tibiae were cut at 15 μ on a freezing microtome. Decalcified tibiae embedded and blocked in paraffin wax were sectioned at 15 μ on a base sledge microtome. The enzymes were demonstrated using the coupling azo dye method given by Pearse (Histochemistry, 1st Ed. 1954). The stable diazotates of 4 benzoyl amino 2-5 diethoxyanilene, 3 nitro toluidine and o-dianisidine were used. Of the embedding procedures paraffin wax embedding produced the greatest loss of both enzymes. Gelatine embedding and infiltration with celloidin were equally good for the demonstration of acid phosphatase but for alkaline phosphatase the celloidin method was superior. The gelatine embedded material did not produce consistently good results. Celloidin-impregnated tibiae could be stored without marked deterioration of the enzyme content for longer than gelatine-embedded tibiae.     

An Improved Pollen Grain Smear Method for Wheat

Anthers containing actively dividing pollen grains were treated 1 hour at 18-20° C. with 0.2% solution of colchicine, washed 1 hour in water, soaked in 0.002 M aqueous solution of 8-oxyquinoline at 10-14° C. for 1 hour, washed in water for 1 hour and then fixed in Carnoy's solution (alcohol, chloroform, acetic acid, 6:3:1) for 6 hours to overnight. They were washed successively in acetic-alcohol (1:1) 10-15 minutes, 70% alcohol 10-15 minutes and in water 30 minutes before hydrolysing them in bulk in 1 N HCl at 60° C. for 10-15 minutes. “Finally, they were stained in leuco-basic fuchsin for 15-30 minutes. Pollen grains were squeezed out of a stained anther in a small drop of egg albumen on a slide and the albumen smeared uniformly on the slide. The slide was dipped successively for a few seconds in glacial acetic acid and 45% acetic acid respectively. The smear was covered by a cover glass in a drop of aceto-carmine and pressed gently between folded filter papers. The cover glass was sealed with paraffin and stored overnight. To make the preparation permanent the paraffin was removed and the cover glass separated in a 1:1 mixture of acetic acid and n-butyl alcohol. The slide and the cover glass were then passed through n-butyl alcohol, 2 changes, and finally remounted in balsam.     

Low Temperature Sulfation of Tissues and the Demonstration Of Metachromasy

Sulfation of tissue sections which contained nonmetachromatic polysaccharides was done in an equivolume mixture of concentrated sulfuric acid and glacial acetic acid at 0°C. The sections were washed successively in glacial acetic acid and water. Aqueous solutions of toluidine blue, 1.5 × 10^-4 M, were used for staining. The procedure produced a metachromatic substrate in sites previously nonmetachromatic. Normal metachromasy was unaffected. There was no loss, damage or distortion of the tissue sections.     

Solid Substrate Formulations of the Mycoherbicide Colletotrichum truncatum for Hemp Sesbania ( Sesbania exaltata ) Control

Colletotrichum truncatum was grown on kernels of eight different grains for 3 or 4 weeks at room temperature (22-24°C). Fresh preparations of conidia as well as fungus-infested corn and rice suspensions resulted in 100% mortality of hemp sesbania seedlings when sprayed postemergence with a 14 h dew period. Fresh preparations of mycelia and fungus-infested sorghum suspensions resulted in 90 and 65% mortality of hemp sesbania seedlings, respectively. Lower mortality ( ≤15%) occurred with the other ground fungus-infested grain suspensions. Fresh preparations of conidia, fungus-infested corn, rice and sorghum, and mycelia, when applied to soil pre-emergence, resulted in 100, 94, 100, 83 and 71% mortality of hemp sesbania seedlings 14 days after application, respectively. Lower mortality ( ≤23%) occurred with the other ground fungus-infested grain preparations. Freshly-prepared C. truncatum at 6.25, 12.5, 25 and 50 mg fungus-formulated rice cm -2 of soil surface, applied pre-emergence or at the time of planting, killed 97, 100, 100 and 100% of hemp sesbania, respectively. After storage at 22-24°C for 6 to 24 months, the rice formulation caused 67 to 93% mortality after 6 months, 39 to 81% after 12 months, and ≤2% after 24 months, respectively. When C. truncatum was refrigerated at 4-6°C, the rice formulation retained good efficacy through 24 months, and when frozen, for up to 8 years. C. truncatum formulated on rice stored under all the above conditions contained mainly sclerotia at 2.4 x 10 5 sclerotia g -1 . C. truncatum killed hemp sesbania seedlings with a single soil application through 4 plantings on the same soil. These results indicate that rice and possibly corn are excellent solid substrates for the formulation of C. truncatum . This is a simple and effective method for enhancing the activity of C. truncatum against hemp sesbania.     

The Peracetic-Orcein-Halmi Stain: A Stain for Connective Tissues

A selective stain useful for the study of connective tissues is described. The stain demonstrates elastic and oxytalan fibers as well as fibrils in mucous connective tissues previously undescribed. Reticular fibers are not stained. The stain may be used on sections that have been fresh frozen or fixed in formalin or ethanol. Sections are deparaffinized, washed in absolute ethanol, oxidized in peracetic acid 30 min, washed in running water, stained in Taenzer-Unna orcein 15 min, 37°C, differentiated in 70% ethanol, washed in running water, stained in Lillie-Mayer alum hematoxylin 4 min, blued in running water, and counterstained 20 sec in a modified Halmi mixture of 100 ml distilled water, 0.2 gm light green SF, 1.0 gm orange G, 0.5 gm phosphotungstic acid and 1.0 ml glacial acetic acid. Sections are rinsed briefly in 0.2% acetic acid in 95% ethanol, dehydrated and mounted.     

Comparison of endogenous polyamine content in hazel leaves and buds between the annual dormancy and flowering phases of growth

Upon exposure to air at 20°C and 60% relative humidity (RH), an occlusion to water uptake developed in the basal stem segment of cut, flowering Sonia roses. The development of the occlusion was delayed by removing the leaves before storage, indicating an effect of transpiration. Placing the stem ends at 100% RH during exposure to air had no effect, which shows that water loss through the cut end is not the cause. Scanning electron microscopy did not show plant gums or tyloses in the water conducting elements.
The hypothesis by Scholander et al. (1955) that water uptake into stems held in air and then placed in water occurs through conduit walls rather than the lumen was tested by using stems of which the cut surface was covered with laboratory grease and a ring of bark was removed (girdling). Girdled stems placed in water remained fully turgid when the girdled area was about 60 mm² or more. Water uptake was strongly inhibited when the girdled stems were exposed to air for 24–36 h, as in non-girdled controls exposed to air for the same period. Inclusion of a surfactant (nonylphenoxypolyethoxy ethanol) in the vase water, however, facilitated water uptake after dry storage of normal cut flowering stems but did not improve water uptake into the girdled stem system, which is inconsistent with the hypothesis.
It is concluded that the vascular occlusion developing upon exposure to air cannot be explained by decreased flow in the wall pathway for water.     

A One-Solution Triacid General Stain Which Differentiates Oxygenated from Non-Oxygenated Red Blood Corpuscles

Tissues from representative mammals, amphibia and invertebrates were fixed for 5-24 hr in either an aqueous solution of 8% p-toluene sulfonic acid (PTSA) or in 10% formalin to which 5 gm PTSA/100 ml had been added, and processed through embedding in polyethylene glycol 400 distearate in the usual manner. Sections cut at 4-6 μ were floated on 0.2% gelatin containing 1.25% formalin, and spread and dried on slides at a temperature not exceeding 25 C. Wax was removed with xylene, and the sections brought to water through ethanol as usual. The working staining solution was made from three stock solutions: A. Chlorantine fast blue 2RLL, 0.5%; B. Cibacron turquoise blue G-E, 0.5%; C. Procion red M-P, 0.5%—each of which was dissolved in 98.5 ml of distilled water to which 0.5 ml of glacial acetic acid and 0.5 ml of propylene glycol monophenyl ether (a fungicide) had been added. For use, the three solutions were mixed in the proportions: A, 3; B, 4; and C, 3 volumes. Staining time was uncritical, 10-30 min usually sufficing for 6 μ, sections. The chief feature of the staining is the differentiation of oxygenated and nonoxygenated red blood corpuscles, in reds and blues respectively. Connective tissue stained blue or blue-green and mucin, green. Nuclei and cytoplasm stain according to their condition at the time of fixation. The mixed stain keeps well, remaining active after 2 yr of storage.     

Alcoholic Thionin Counterstaining Following Golgi Dichromate-Silver Impregnation

Brains of cats that had been fixed 2 months or longer in 10% formalin were cut into 3-6 mm. slices and impregnated by Golgi's dichromate-silver procedure (6% dichromate solution, 4-6 days; 1.5% silver nitrate solution 2 days). Sections 100 µ thick were cut after embedding in low melting point paraffin. Three changes of xylene and three of absolute alcohol were followed by staining 3-5 minutes in a saturated solution of thionin in absolute alcohol. The sections were dipped quickly in absolute alcohol and cleared in xylene, then differentiation was effected by an equal-parts mixture of absolute alcohol and xylene. A final clearing in three changes of xylene and mounting in Permount completed the process. Counter-staining was most successful when applied to freshly cut sections.     

Efficacy of diatomaceous earth to control internal infestations of rice weevil and maize weevil (Coleoptera: Curculionidae)

Densities of 10, 20, and 30 hard red winter wheat kernels, Triticum aestivum L., were infested with different life stages of the rice weevil, Sitophilus oryzae (L.), mixed with 35 g of wheat treated with 300 ppm of the Protect-It (Mississauga, Ontario, Canada) formulation of diatomaceous earth (DE), and held at 22, 27, and 32 degrees C. A similar test was conducted by exposing densities of 6, 12, and 18 corn kernels infested with different life stages of the maize weevil, Sitophilus zeamais Motschulsky, mixed with 30 g of corn, Zea mays L., treated with 300 ppm of DE. Mortality of adults emerging from kernels in wheat treated with DE was always greater than controls, and ranged from 56 to 90% at 22 degrees C and was >90% at 27 and 32 degrees C. In most treatment combinations, exposure to DE suppressed F1 progeny by 60-90% relative to untreated controls. Mortality of adult maize weevils on treated corn held at 22 and 27 degrees C was lower than mortality of rice weevils on wheat, and ranged from 4 to 84%. F1 production was low in corn held at 22 degrees C, and no F1s were produced in either the controls or the treatments at 32 degrees C. In treated corn held at 27 degrees C, exposure to the DE suppressed F1 progeny by approximately 70-80% relative to the untreated controls. Results of this study show that rice weevils and maize weevils emerging from infested kernels as adults are susceptible to DE, and these results are comparable to other studies in which adult weevils were exposed directly on wheat or corn treated with DE. Although adult weevils will be killed by exposure to DE, some oviposition could still occur and progeny suppression may not be complete; however, application of DE to commodities already infested with internal feeders, such as the rice weevil and the maize weevil, could help eliminate or suppress the infestation.     

A Plastic Embedding Medium for Thin Sectioning in Light Microscopy

Tissue blocks with surface areas up to 2 cm² can be sectioned at 1 or 2 μ after embedding in a medium consisting of: methyl methacrylate, 27 ml; polyethylene glycol distearate MW 1540, 6 gm; dibutyl phthalate, 4 ml; and Plexiglas molding powder A-100, 9 gm (added last). The methacrylate mixture is polymerized at 50° C by benzoyl peroxide, 0.8 gm/ 100 ml of methacrylate. The polymerized matrix is transparent and the blocks can be cut on a rotary microtome with a steel knife. The plastic can be removed from sections with acetone prior to staining. Artifacts caused by embedding and sectioning are negligible     

Imaging and automated detection of Sitophilus oryzae (Coleoptera: Curculionidae) pupae in hard red winter wheat

Computed tomography, an imaging technique commonly used for diagnosing internal human health ailments, uses multiple x-rays and sophisticated software to recreate a cross-sectional representation of a subject. The use of this technique to image hard red winter wheat, Triticum aestivm L., samples infested with pupae of Sitophilus oryzae (L.) was investigated. A software program was developed to rapidly recognize and quantify the infested kernels. Samples were imaged in a 7.6-cm (o.d.) plastic tube containing 0, 50, or 100 infested kernels per kg of wheat. Interkernel spaces were filled with corn oil so as to increase the contrast between voids inside kernels and voids among kernels. Automated image processing, using a custom C language software program, was conducted separately on each 100 g portion of the prepared samples. The average detection accuracy in the five infested kernels per 100-g samples was 94.4 +/- 7.3% (mean +/- SD, n = 10), whereas the average detection accuracy in the 10 infested kernels per 100-g sample was 87.3 +/- 7.9% (n = 10). Detection accuracy in the 10 infested kernels per 100-g samples was slightly less than the five infested kernels per 100-g samples because of some infested kernels overlapping with each other or air bubbles in the oil. A mean of 1.2 +/- 0.9 (n = 10) bubbles (per tube) was incorrectly classed as infested kernels in replicates containing no infested kernels. In light of these positive results, future studies should be conducted using additional grains, insect species, and life stages.     

Methacrylate Embedding and Sectioning of Calcified Bone

Twenty-five milliliter aliquots of ethyl-butyl (1:1) methacrylate were polymerized at 6 or 7 initiator concentrations using 3 polymerization temperatures, both in air and in a water bath. Duplicate series were polymerized with and without vibration, pre-polymerization, and exclusion of oxygen. Hardening times and maximum temperatures reached within the samples were recorded. Vibration and the exclusion of oxygen had no effect. Prepolymerization, increasing polymerization temperature and increasing initiator concentration all decreased the hardening time and increased the maximum temperature. Polymerizing in a water bath rather than in air reduced the maximum temperature by 25-40°C and lengthened the hardening time about 1 hr. An initiator concentration of 0.4% Luperco CDB in ethyl-butyl methacrylate and a water-bath temperature of 45°C were selected for tissue embedding. The hardening time was 8 hr and the maximum temperature during polymerization was about 60°C.

Split rat femora and tibiae were freeze-dried and vacuum-infiltrated with acetone, absolute alcohol or monomer. The acetone or alcohol-fixed specimens were subsequently infiltrated with monomer. The specimens were transferred to 1 oz bottles, prepolymerized syrup added, and polymerized. No consistent differences between specimens treated by these methods were noted. Five-micron serial sections could be cut using a Leitz sledge microtome with a modified knife if the block was coated with paraffin between sections.     

Acetic Acid as a Diluent and Dehydrant in the Preparation of Whole, Stained Helminths

Aqueous 45% acetic acid can be used successfully as a diluent for Ehrlich's haematoxylin and for Horen's trichrome stain (chromotrope 2 R, 0.6 gm; phosphotungstic acid, 0.7 gm; glacial acetic acid, 1.0 ml; water, 100 ml). Glacial acetic acid is used for dehydration of the stained helminths, and followed by a glacial acetic acid-methyl salicylate series for clearing. The whole process can be completed within 1 hr, from fixation to the cleared specimen, with helminths up to 5 mm in length. A satisfactory fixative for Monogenea, Digenea and Acanthocephala is: 85% ethanol, 85; formalin (40% HCHO), 10; and glacial acetic acid, 5—parts by volume. For Cestoda, 5% aqueous formalin is preferable because they are hardened excessively by the alcoholic fixative.     

Growth enhancement and antitranspirant activity following seed treatment with a derivative of 5-hydroxybenzimidazole (Ambiol) in four drought-stressed agricultural species

The biostimulating action of seed treatment with the synthetic antioxidant, Ambiol (2-methyl-4-Edimethylaminomethyl-5-hydroxybenzimidazole dihydrochloride) on subsequent growth and transpiration of seedlings was studied. To study growth and transpiration responses, seeds of four agricultural species, soybean ( Glycine max L.), rapeseed ( Brassica napus L.), winter wheat ( Trilicum aestivum L.) and corn ( Zea mays L.), were soaked in Ambiol for 24 h, using the following concentrations: 0, 0.01, 0.1, 1, 10 and 100 mg 1¹. The subsequent seedlings were subject to simulated soil drought, using computer-automated root misting chambers. The influence of Ambiot on transpiration rate under simulated air drought was studied by growing plants under low humidity in a controlled humidity chamber. Response to Ambiol varied, depending on its concentration, the species used and the environment. Compared to untreated plants, 10 mg 1-⁻¹ Ambiol reduced the mid-day transpiration rate and total daily water usage of soybean by approximately 25%. Under simulated soil drought in the root misting chamber, 10 and 100 mg 1-⁻¹ Ambiol increased growth of rapeseed and soybean by 25–45%, relative to the 0 mg 1-⁻¹ treatment, yielding plants comparable in size to the fully-irrigated controls. However, Ambiol failed to promote growth of two drought-stressed monocotyledons (corn and winter wheat). At 100 mg P. Ambiol inhibited growth of both well-watered wheat and rapeseed, although this inhibition was mitigated by drought.     

Interaction effects of lactic acid and acetic acid at different temperatures on ethanol production by <Emphasis Type="Italic">Saccharomyces cerevisiae</Emphasis> in corn mash

The combined effects of lactic acid and acetic acid on ethanol production by S. cerevisiae in corn mash, as influenced by temperature, were examined. Duplicate full factorial experiments (three lactic acid concentrations × three acetic acid concentrations) were performed to evaluate the interaction between lactic and acetic acids on the ethanol production of yeast at each of the three temperatures, 30, 34, and 37°C. Corn mash at 30% dry solids adjusted to pH 4 after lactic and acetic acid addition was used as the substrate. Ethanol production rates and final ethanol concentrations decreased (P<0.001) progressively as the concentration of combined lactic and acetic acids in the corn mash increased and the temperature was raised from 30 to 37°C. At 30°C, essentially no ethanol was produced after 96 h when 0.5% w/v acetic acid was present in the mash (with 0.5, 2, and 4% w/v lactic acid). At 34 and 37°C, the final concentrations of ethanol produced by the yeast were noticeably reduced by the presence of 0.3% w/v acetic acid and ≥2% w/v lactic acid. It can be concluded that, as in previous studies with defined media, lactic acid and acetic acid act synergistically to reduce ethanol production by yeast in corn mash. In addition, the inhibitory effects of combined lactic and acetic acid in corn mash were more apparent at elevated temperatures.     

Effect of Air Humidity on the Infection Potential of Hyphomycetous Fungi as Mycoinsecticides for Trialeurodes vaporariorum

Two commercial mycoinsecticides, 'Mycotal', based on Verticillium lecanii and 'Naturalis-L', on Beauveria bassiana, were used at dosages recommended by manufacturers to examine effects of a range of medium and high humidities on infection towards Trialeurodes vaporariorum. Two series of bioassays were carried out using special devices. In one series, a non-excised bean leaf was sandwiched in order to create a chamber above the whitefly-infected area. In another series, three potted whole bean plants were maintained in an airtight plastic box. In both series, conducted at 25°C, relative humidity (RH) was controlled by injecting a circulating constant flow of humidity-regulated air which had passed over a salt solution used to maintain targeted air humidity levels (ranging from 53 to 98.5 and 75 to 98.5% RH, respectively). Microclimatic measurements demonstrated that non-excised leaves significantly increased the air humidity in the air circulating in the immediate environment of the leaf surface as well as that of the whole plant. In the first series of assays under all RH conditions tested (from 70 to 98% RH after passage above the leaves), both mycoinsecticides induced high mortality rates (92-100%). The fungal effect occurred early, since at least 70% of whiteflies died as second instars, before the next molt occurred. Fungus-induced mortality appeared to be independent of the expected humidity level. In the second series of assays, mortality rates were high (98-100%) and did not depend on the ambient humidity conditions tested (from 80 to 100% RH). Mortality rates occurring during the second instar ranged from 46 to 88%. Implication of these results for microbial control of whiteflies in greenhouses and in the field is discussed in relation to plant transpiration-induced increase in air humidity prevailing in the habitat of the targeted whitefly larvae.     

An Ice-Solvent Method of Drying Frozen Tissue for Plant Cytology

A freeze-dry method where cold absolute ethanol is used as a dehydrating agent in place of vacuum dehydration has been applied to various plant materials with good cytological results. The method involves: (a) freezing rapidly small pieces of tissue 1 cubic mm or less in partly frozen isopentane cooled with liquid nitrogen, (b) transferring quickly to vials of cold absolute ethanol at -41° to -45°C, and (c) holding within this temperature range for 3 days to dissolve the ice. A simply constructed cryostat is used to maintain the vials of absolute alcohol and tissue at the cold temperature. This consists of a semi-frozen constant temperature bath of either 65% ethanol or pure diethyl oxalate in a tightly covered beaker which fits within a large dewar flask half filled with dry ice. The bath is arranged so that it will be on top of and in contact with the dry ice but properly insulated to prevent freezing completely.

The resulting dried tissue is very unstable in either water or hot absolute ethanol; therefore, to prevent loss of cytological detail during further processing, the tissue must be treated to render the proteins insoluble. Either (a) replace the cold absolute ethanol in the tissue vials with cold (approx. -40°C) 75% ethanol, warm slowly to 60°C, and hold for 1 hour, or (b) replace with cold acidulated 95% ethanol (100 ml. of 95% ethanol + 0.30 ml. of glacial acetic acid), warm to room temperature, and hold for 30 minutes. Following either treatment the tissues are dehydrated to absolute alcohol and embedded in paraffin by the usual technics. Sections are attached to slides by flattening over warm water and drying.

When epidermis from onion bulbs was used as a basis of comparison of fixed and living material with the phase-contrast microscope, the mitochondria, plastids, and other fine structures in fixed preparations appear to be nearly identical with the living. Fat droplets disappear. With larger tissues such as onion root tips, thin freehand sections must be prepared before freezing to obtain good cytological results. The application of the method to cytochemical studies is discussed and in many ways it seems to be as useful as the freeze vacuum-dry method.