Effects of Fixation on Cell Volume of Marine Planktonic Protozoa

The effects of fixation on the cell volume of marine heterotrophic nanoflagellates and planktonic ciliates were investigated. Decreases in cell volume depended on the combination of the protozoan taxa and the particular fixative. For a particular fixative and protozoan species, degree of shrinkage was independent of physiological state. The volume of fixed cells was found to be approximately 20 to 55% lower than the cell volume of live organisms. For the heterotrophic microflagellates, the fixatives ranked, in order of decreasing effect on cell volume, as glutaraldehyde, formaldehyde, acid Lugol's solution, and modified van der Veer solution. With oligotrichous ciliates and a tintinnid ciliate, formaldehyde caused less shrinkage than glutaraldehyde or acid Lugol's solution. With the aldehyde fixatives, the microflagellates were found to shrink more than the ciliates. Differential effects of fixation on cell volumes may result in an underestimation of the biomass of certain protozoan taxa in natural samples.     

The annual cycle of planktonic ciliates in nearshore waters at Signy Island, Antarctica

The abundance and biomass of marine planktonic ciliates in BorgeBay, Signy Island, were determined at monthly intervals betweenApril 1990 and June 1991. At least 24 different ciliate taxawere recorded from samples preserved in Lugol's iodine, includingthe tintinnids Codonellopsis balechi, Cymalocylis convallaria,Laackmaniella naviculaefera and Salpingella sp., and the aloricatetaxa Didinium sp. and Mesodinium rubrum. Ciliate abundance andbiomass exhibited a clear seasonal cycle with high values duringthe austral summer and low values in the austral winter. Abundanceranged from 0.3 10³l^–1 in September to 2.3 10³l^–1in January, while biomass ranged from 0.5 µg C l^–1in October to 12.6 µg C l^–1 in December. Small ciliatesdominated abundance throughout the year, and biomass duringwinter. Larger ciliates contributed most to biomass during summer.Aloricate ciliates were common throughout the year, while tintinnidscontributed substantially to abundance and biomass only duringsummer. Salpingella sp. was the commonest tintinnid, but C.convallariacontributed most to tintinnid biomass. The seasonal patternof ciliate abundance and biomass matched that of chlorophylla concentration and bacterial biomass, suggesting tight trophiccoupling between ciliates and other components of the pelagicmicrobial community. ¹Present address: Scott Polar Research Institute, Universityof Cambridge, Lensfield Road, Cambridge CB2 1ER, UK     

Evaluation of double formalin--Lugol's fixation in assessing number and biomass of ciliates: an example of estimations at mesoscale in NE Atlantic

Ciliated protozoa are potential grazers of primary and bacterial production and act as intermediaries between picoplankton and copepods and other large suspension feeders. Accurate determination of ciliate abundance and feeding mode is crucial in oceanic carbon budget estimations. However, the impact of different fixatives on the abundance and cell volume of ciliates has been investigated in only a few studies using either laboratory cultures or natural populations. Lugol's solution and formalin are the most commonly used fixatives for the preservation of ciliates samples. In the present study, the aim was to compare 0.4% Lugol's solution and 2% borated-formalin fixation and evaluate the need of counting duplicate samples each using a different fixative. For this, a large number of samples (n = 110) from the NE Atlantic was analyzed in the frame of POMME program (Multidisciplinary Mesoscale Ocean Program). We established a statistically significant relationship (p < 0.0001) between Lugol's and formalin fixed samples for both abundance (r2 = 0.50) and biomass (r2 = 0.76) of aloricate ciliates which showed that counts were higher in Lugol's solution by a factor of 2 and a non-taxon specific cell-loss in formalin. However, loricate ciliate abundance in our samples which were represented primarily by Tintinnus spp. did not show any difference between the two treatments. Abundance and biomass of mixotrophic ciliates (chloroplast-bearing cells) were for various reasons underestimated in both treatments. Our results show that unique fixation by formalin may severely underestimate ciliates abundance and biomass although their population may not alter. For this reason, Lugol's solution is best for the estimation of their abundance and biomass. However, for counts of mixotrophs and the evaluation of the ecological role of ciliates in carbon flux, double fixation is essential. Compromises regarding the fixatives have lead to severe underestimations of mixotrophs in studies conducted by now.     

The influence of fixation and tissue preparation on the immunohistochemical demonstration of fibronectin in human tissue

The influence of fixation and tissue preparation on the immunohistochemical localization of human fibronectin in gastrointestinal tract tissue has been examined using indirect immunoperoxidase technique. The most optimal staining result with strong intensity and well defined localization was obtained on frozen sections of unfixed material. Nearly identical results with improved morphology were obtained when staining paraffin sections of tissue fixed in 96% ethanol, 96% + 1% acetic acid and absolute acetone. All other fixatives tested, 10% neutral buffered formalin. Lillie's AAF, Bouin's fixative, Clarke's fixative, 4% formaldehyde, 4% formaldehyde + 0.5% cetylpyridiniumchloride (F-CPC), 4% formaldehyde +0.1% glutaraldehyde gave unsatisfactory results. However, proteolytic digestion with pepsin of paraffin sections prior to staining of buffered formalin and F-CPCfixed material gave results comparable with those obtained on unfixed frozen sections are regards definition of the staining whereas staining intensity was decreased in some degree. No improvement was observed when using proteolytic digestion of tissue fixed in other fixatives.     

The influence of fixation and tissue preparation on the immunohistochemical demonstration of fibronectin in human tissue

Summary The influence of fixation and tissue preparation on the immunohistochemical localization of human fibronectin in gastrointestinal tract tissue has been examined using indirect immunoperoxidase technique. The most optimal staining result with strong intensity and well defined localization was obtained on frozen sections of unfixed material. Nearly identical results with improved morphology were obtained when staining paraffin sections of tissue fixed in 96% ethanol, 96%+1% acetic acid and absolute acetone. All other fixatives tested, 10% neutral buffered formalin, Lillie's AAF, Bouin's fixative, Clarke's fixative, 4% formaldehyde, 4% formaldehyde+ 0.5% cetylpyridiniumchloride (F-CPC), 4% formaldehyde +0.1% glutaraldehyde gave unsatisfactory results. However, proteolytic digestion with pepsin of paraffin sections prior to staining of buffered formalin and F-CPCfixed material gave results comparable with those obtained on unfixed frozen sections as regards definition of the staining whereas staining intensity was decreased in some degree. No improvement was observed when using proteolytic digestion of tissue fixed in other fixatives.     

Seasonal variation in the species composition of tintinnid cilates in Hiroshima Bay, the Seto Inland Sea of Japan

Seasonal changes in the species composition of tintinnid ciliateswere examined based on time-series samples taken at 2 week intervalsover a 3 year period in Hiroshima Bay, the Seto Inland Sea ofJapan. The maximum abundance of total tintinnids over the entireperiod was 5.7 x 10³ indi viduals l^– Among 32 speciesidentified, a consistent seasonal occurrence was recognizedin 22 species. The relationships between various environmentalfactors and the abundance of each species of tintinnids wereanalyzed using principal component analysis From this analysis,the abundance of many tintinnids was revealed to be associatedwith temperature, the <20 µm size fraction of chlorophylla and water column stability, but not with the <20 µmsize fraction of chlorophyll a, nor with salinity. From theseresults, tintinnid species were divided into five associationtypes: species whose abundance increased with increasing temperature,decreasing temperature, nanophytoplankton abundance, increasingwater column mixing, or increasing water stratification coupledwith low temperature.     

Comparison of the effects of two fixatives for immunolocalization of testosterone in the testes of the cynomolgus monkey, mouse and rat.

We compared the effect of two fixatives, Bouin's fixative and neutralized buffered 4% formaldehyde (10% formalin), for immunolocalization of testosterone in the testes of cynomolgus monkeys, mice and rats. In the samples fixed with Bouin's fixative, immunoreactive testosterone was detected as intense deposits in the cytoplasm of Leydig cells of monkeys and mice. Immunoreactive testosterone was detected not only in Leydig cells of rats but also moderately shown within tubules. Immunoreactive testosterone could not be detected in the testes of monkeys, mice or rats fixed with neutralized buffered formalin because of the poor morphology caused by the fixative. It is concluded that Bouin's fixative is a suitable fixative for immunolocalization of testosterone in the testes of cynomolgus monkeys, mice and rats.     

Improved utilization of tissue blocks for electron microscopy. Effect of various concentrations of formaldehyde and glutaraldehyde.

Liver tissue from miniature pig fetuses was immersion-fixed in fixative mixtures with various concentrations of formaldehyde and glutaraldehyde. The preservation quality of hepatocytes was evaluated ultrastructurally in a peripheral zone (30--130 micron below the surface) and a central zone (500 micron below the surface). In the peripheral zone the best preservation was obtained with a fixative mixture containing 2% formaldehyde and 2% glutaraldehyde and in the central zone with a fixative mixture containing 8% formaldehyde and 8% glutaraldehyde. It is concluded that a better utilization of fairly large tissue blocks for ultrastructural investigation can be obtained by division of the block and subsequent fixation in fixatives containing various concentrations of formaldehyde and glutaraldehyde.     

东海原甲藻(Prorocentrum donghaiensis)对原生动物群落结构影响的现场船基实验

2005年在长江口赤潮频发海域调查期间,分别于4月27日、5月4日和5月8日,在zzf1、zc18a和ra5站位利用现场船基培养的方法,研究了添加到赤潮密度10^6cells L^-1的东海原甲藻（Prorocentrum donghaiense）对原生动物群落结构的影响。结果发现,赤潮密度的东海原甲藻抑制了小型无壳纤毛虫的种群数量,而没有抑制中大型砂壳纤毛虫和夜光虫（Noctiluca scintillans）的种群数量,从而使得原生动物群落向中大型种类演替,这种影响的程度与原生动物本身的群落组成和浮游植物的组成密切相关。添加东海原甲藻72h后,在以小型无壳纤毛虫管游虫（Cyrtostrombidium sp．）为优势种的zzf1站位,演替为以大型原生动物夜光虫为优势种的群落;在以中大型原生动物百乐拟铃虫（Tintinnospsis beroidea）和夜光虫为优势种的zc18a站位,仍然是以此为优势种,且大型原生动物夜光虫在群落中的比例上升;在以小型无壳纤毛虫急游虫2（Strombidium sp．2）为优势种的ra5站位,演替为以中大型原生动物百乐拟铃虫和亚速岛网纹虫（Favella azorica）为优势种的群落。zzf1和ra5站位实验组中原生动物的总丰度都呈下降趋势,而zc18a站位变化不明显,这是由于前两个站位的最优势种管游虫（zzf1站位）和急游虫2（ra5站位）的丰度迅速下降,而zc18a站位的优势种百乐拟铃虫和夜光虫的丰度比较稳定造成的。在zzf1和zc18a站位,对照组和实验组中原生动物的总生物量在实验前后都没有大的变化,而在ra5站位却均呈下降的趋势。这可能与浮游植物的组成有关,zzf1和zc18a站位是以无毒的锥状斯氏藻（Scrippsiella trochoidea）和螺旋环沟藻（Gyrodinium spirale）为主,而ra5站位是以有毒的亚历山大藻（Alexandriumsp．）为主。综上可见,可预测当东海大规模赤潮爆发时,会使原生动物群落向中大型种类演替,进而可能影响海洋生态系统的结构和功能。     

Effects of Aldehyde Fixation on Adenosine Triphosphatase and Peroxidase Activities in Maize Root Tips

The effects of aldehyde fixation of excised roots and subcellularfractions of Zea mays have been studied in relation to the preservationof ATP-ase and peroxidase activities. Total peroxidase was littleaffected by either formaldehyde or glutaraldehyde whereas ATP-aseshowed considerable loss of activity, particularly with glutaraldehyde.The activity remaining after fixation was dependent on boththe concentration of fixative and the pH of fixation. Subcellularfractions differed in their response to fixation with the cellwall fraction generally showing higher retention of activitythan the mitochondrial or microsomal fractions.     

Volumetric Instillation of Fixatives and Inert Substances Into Mouse Lungs

Mouse lungs were instilled with various fixatives to establish the optimum volume necessary to fix the lung without distortion and to compare the efficacy of the fixatives. Fixation with either Stieve's or Bouin's fluid was found preferable to 2.5% and 5% glutaraldehyde, 4% neutral buffered formalin, and to a mixture of formalin and Stieve's fixative. In addition, a comparison was made between diluted Ames O.C.T. Compound and 4% aq. gelatin as supportive substances for unfixed lungs in preparation of cryostat sections and for histochemistry. A 1:2 dilution of O.C.T. was found to be superior to 4% gelatin in preparative, cutting and adhesive properties. The optimal instilled volume for mouse lungs was found to be 0.1 ml for every 7 grams of body weight, introduced at a rate of 0.1 ml per 10 seconds.     

东海原甲藻（Prorocentrum donghaiensis）对原生动物群落结构影响的现场船基实验

2005年在长江口赤潮频发海域调查期间,分别于4月27日、5月4日和5月8日,在zzf1、zc18a和ra5站位利用现场船基培养的方法,研究了添加到赤潮密度106 cells L-1的东海原甲藻（Prorocentrum donghaiense）对原生动物群落结构的影响。结果发现,赤潮密度的东海原甲藻抑制了小型无壳纤毛虫的种群数量,而没有抑制中大型砂壳纤毛虫和夜光虫（Noctiluca scintillans）的种群数量,从而使得原生动物群落向中大型种类演替,这种影响的程度与原生动物本身的群落组成和浮游植物的组成密切相关。添加东海原甲藻72 h后,在以小型无壳纤毛虫管游虫（Cyrtostrombidium sp.）为优势种的zzf1站位,演替为以大型原生动物夜光虫为优势种的群落;在以中大型原生动物百乐拟铃虫（Tintinnospsis beroidea）和夜光虫为优势种的zc18a站位,仍然是以此为优势种,且大型原生动物夜光虫在群落中的比例上升;在以小型无壳纤毛虫急游虫2（Strombidium sp.2）为优势种的ra5站位,演替为以中大型原生动物百乐拟铃虫和亚速岛网纹虫（Favella azorica）为优势种的群落。zzf1和ra5站位实验组中原生动物的总丰度都呈下降趋势,而zc18a站位变化不明显,这是由于前两个站位的最优势种管游虫（zzf1站位）和急游虫2（ra5站位）的丰度迅速下降,而zc18a站位的优势种百乐拟铃虫和夜光虫的丰度比较稳定造成的。在zzf1和zc18a站位,对照组和实验组中原生动物的总生物量在实验前后都没有大的变化,而在ra5站位却均呈下降的趋势。这可能与浮游植物的组成有关,zzf1和zc18a站位是以无毒的锥状斯氏藻（Scrippsiella trochoidea）和螺旋环沟藻（Gyrodinium spirale）为主,而ra5站位是以有毒的亚历山大藻（Alexandrium sp.）为主。综上可见,可预测当东海大规模赤潮爆发时,会使原生动物群落向中大型种类演替,进而可能影响海洋生态系统的结构和功能。     

Evaluation of fixative composition,fixative storage,and fixation duration on the fine structure and volume of root-cell nucleoli

Summary— The effect of various combinations of three fixative compositions (glutaraldehyde buffered in veronal acetate, cacodylate, and piperazine-N, N'-bis[2-ethanesulfonic acid]—PIPES], two fixative storage times (fresh vs 6 weeks), and two fixation durations (3 h vs 9 days) on nucleolar fine structure and nucleolar volume in three root cell-types of oat seedlings (Avena sativa L, cv Seger) were evaluated. All fixatives show overall good preservation of fine structure. Nucleolar components are distinct and well delineated in cells fixed in solutions buffered with either cacodylate or veronal acetate; the components are more condensed when preserved in fixative buffered with PIPES. Nucleolar volume is greatest in cells fixed in the cacodylate fixative, and smallest in those preserved in the PIPES fixative. Among the treatments tested, the PIPES fixative evidently best maintains nucleolar volume. Distracting particulate deposits are abundant on nuclei and nucleoli in cells preserved in the veronal-acetate fixative. Contrary to common assumptions, aging of buffered fixative at room temperature for 6 weeks seems to affect neither the general quality of cellular preservation nor the pH of the fixatives, although nucleolar volume is reduced by such treatment. Long-period fixation (9 days) results in destruction of membrane integrity (mitochondria, plastids, ER), and shrinkage of organelles from the cytoplasm. Nucleolar volume is reduced with prolonged fixation.     

Factors controlling pelagic populations of ciliates and heliozoans-- late summer investigations in an acidic lake before and after liming

Ciliates and heliozoans were studied in a small oligotrophicSwedish lake with the objective of investigating what controlledthe community structure and population dynamics. Enclosure experimentswere performed with five levels of inorganic nutrient concentrationsand the presence or absence of crustacean zooplankton. The experimentswere performed during the summers immediately preceding andfollowing liming of the lake. The responses of protozooplanktonto these manipulations were investigated and compared with theresponses of bacterioplankton, phytoplankton and metazooplankton.In contrast to most studies on protozoan zooplankton, ciliateswere determined to the lowest taxon possible, and biomassesand abundances were calculated for the different taxa. The protozooplanktonbiomass of the lake, expressed as summer average, did not changebetween the years. However, the community composition changedfrom smaller to larger species as the small prostomatid ciliatesUrotricha and Balanion were largely replaced by oligotrichsof the genera Strombidium and Strobilidium. The experimentssuggested that the protozooplankton community in the lake wascontrolled by metazooplankton in the acidic environment, whilefood limitation was the most important controlling factor afterliming. Before liming, Urotricha and Balanion were unaffectedby nutrient additions as well as by metazooplankton, while otherciliates and Heliozoa showed a significantly negative responseto metazooplankton. After liming, Urotricha and Balanion showeda significant positive response to nutrient addition as wellas to bacterioplankton biomass. A possible explanation for thisresponse in these algivore genera is that the response was indirectand mediated through small chrysoflagellates.     

The impact of different fixation procedures on staining of macromolecules in a microtiter system

Summary The effects of formaldehyde, glutaraldehyde, methanol, Clarke's fixative and microwave irradiation on the quantitative staining of proteins (Naphthol Yellow S) and nucleic acids (Ethyl Green—Pyronin) in a cell culture system have been investigated. Overall, glutaraldehyde rapidly yielded the highest and most consistent levels of staining when compared to all other chemical fixatives. Although microwave irradiation was found to be uneven, 4 min exposure to 700W was found to give higher levels of protein staining than those achieveable with glutaraldehyde. Time-dependent processes were observed with all procedures. In addition, dissociations in the trends of protein and nucleic acid staining were observed. It is suggested that these results domonstrate fixation events that have not previously been resolved from the effects of reagent penetration into tissue blocks.     

The effect of different fixatives and length of fixation time on subsequent AgNOR staining for frozen and paraffin-embedded tissue sections

Summary The AgNOR technique has been used extensively in studies investigating the possibility that the numbers and appearances of the intranuclear structures stained are markers of malignancy. The method has the advantage of being applicable to many different types of histological material, including paraffin-embedded tissue. However, it has been suggested that the visualization of AgNORs is dependent on the type and time of fixation employed. This study set out to measure this effect with the following commonly-used fixatives: acetone, absolute ethanol, methanol, Carnoy's fluid, Bouin's fluid, 4% glutaraldehyde, 10% neutral buffered formalin and 10% formol-saline. Both frozen sections and blocks of fresh tonsil were fixed for varying times, the blocks of tissue then being processed routinely. With the frozen sections AgNORs were easier to discern than in sections of paraffin-embedded tissue, and more intranucleolar AgNORs were visible when alcoholic fixatives were used than with aldehyde fixation. The effects of different fixatives on AgNOR appearance in paraffin sections is, however, more complex. Despite the variation caused by different fixatives, AgNORs could be demonstrated adequately with all the fixatives studied. It is concluded that fixation is not a limitation to the study of AgNORs provided that the time and type of fixative is controlled.     

The effect of formaldehyde containing fixatives on ribonuclease activity

Summary 1. The inactivation of crystalline ribonuclease by formaldehyde and formaldehyde containing fixatives (Serra's solution) is demonstrated.2. The rate of inactivation is shown to be dependent uponph, formaldehyde concentration, and time of action of the fixative.3. The effect of formaldehyde containing fixatives on the RNase activity in sections from fixed tissues is discussed, and the inactivation of that enzyme system in rat pancreas is demonstrated.With 2 Figures in the Text     

Impact of glutaraldehyde versus glutaraldehyde-formaldehyde fixative on cell organization in fish corneal epithelium

The purpose of this study was to examine the impact of a low osmolality glutaraldehyde fixative and a high osmolality glutaraldehyde-formaldehyde fixative on the structural organization of a tissue that could be exposed to low and high osmolality environments. The corneas of freshwater trout were prepared for transmission and scanning electron microscopy using either a fixative of 2% glutaraldehyde in 60 mM cacodylate buffer (pH 7.8, 260 mOsm/l) or a fixative prepared by adding 2.5% glutaraldehyde to a solution of 1% formaldehyde and buffering the solution with 0.1 M cacodylate (pH 7.6, 850 mOsm/l; Karnovsky-type fixative). The corneal epithelial cell layer thickness was greater after glutaraldehyde compared to glutaraldehyde-formaldehyde fixation (67 vs 55 mum), as was the thickness of the superficial cells (5.1 vs 3.4 mum) and basal cells (43 vs 38 mum). The intermediate (wing) cells of the epithelium were, however, less thick after glutaraldehyde fixation (15 vs 18 mum). The width of the squamous, intermediate and basal cells was greater following glutaraldehyde fixation with the effect being greatest in the superficial layers and insignificant at the level of the basal cells. The results show that chemical fixatives with extremes of osmolality cannot only produce different cell sizes in a tissue but also determine the overall organization of the cells in a positional-dependent fashion.     

Rapid quantification of planktonic ciliates: comparison of improved live counting with other methods

THE FOLLOWING EFFICIENT AND QUANTITATIVELY VALID METHOD TO FILTER CONCENTRATE AND COUNT LIVE PLANKTONIC CILIATES WAS DEVELOPED AND COMPARED WITH OTHER TREATMENTS: unconcentrated (raw) samples and centrifuged samples were counted live, and the effects of five different fixatives (HgCl(2), Lugol's iodine, formaldehyde, glutaraldehyde, and Champy-DaFano) on the counts were monitored. Samples originated from a eutrophic mountain lake (Lake Aydat, near Clermont-Ferrand, France). Overall, live filtered counts were similar to counts of raw samples, but they were significantly higher (2 to 2.3 fold, P < 0.05) by analysis of variance than counts from centrifuged samples. Nevertheless, some taxa, i.e., Halteria and Loxodes spp., were sensitive to filtration. The live filtered counts were also comparable to counts of raw HgCl(2)-fixed and settled samples. HgCl(2) and Lugol fixation consistently gave the highest total counts, while significantly lower counts were always obtained with Champy-DaFano-fixed samples. Losses due to fixation were insignificant for raw samples but were substantial and statistically significant in concentrated samples (15% after filtration and 71% after centrifugation, compared with counts from the corresponding live samples). Live counting of passively filter-concentrated ciliates has many advantages over other methods. It is two to four times quicker and more efficient. Ciliates are recognized with certainty, more species are identified, and enumeration of dead organisms (e.g., tintinnid loricas) is avoided. It should be recommended as a quantitatively valid alternative to classical methods for assessing planktonic ciliate populations.     

Evaluation of nine different fixatives. 2. Preservation of IgG, IgA and secretory component in an artificial immunohistochemical test substrate

An artificial substrate was developed for quantitative testing of the ability of various fixatives to preserve the reactivity of IgG and IgA isotypes (gamma and alpha chains) and the secretory component (SC) of secretory IgA as model antigens. Polymerized normal rabbit serum was used as matrix and defined amounts (10-0.1 g/l) of antigen were incorporated into it by diffusion before fixation and paraffin embedding. The various fixatives comprised alcohol, routine formalin, glutaraldehyde(1%)-formalin, Baker's formol calcium, formol sublimate, acetic acid(2%)-formol saline, Bouin's fluid, Susa fixative, and carbodiimide. The detection sensitivity afforded by these fixatives was defined as the immunofluorescence staining end point. Compared to the reference value obtained with alcohol (gamma and alpha chains, 0.06 g/l of IgG and IgA; SC, 0.12 g/l of colostral IgA), an antigen concentration at least 8 times higher was necessary for detection with most of the cross-linking fixatives. Bouin's and Susa fixatives were peculiar in that they required more than 150 times higher antigen concentration for detection of IgG but only 3-8 times higher for IgA. The determined sensitivities were compared with the immunofluorescence performance results obtained on human tissues prepared with the same fixatives; excepting carbodiimide (which produced unacceptable autofluorescence of the substrate matrix) a remarkably good correlation was found with regard to IgG- and IgA-producing cells (especially of the former isotype) and secretory epithelium (IgA and SC). However, the latter result depended on pronase treatment of the tissue sections to unmask epithelial antigens.(ABSTRACT TRUNCATED AT 250 WORDS)