Diameters of microtubules change during rotation of the lipotubuloids of Ornithogalum umbellatum stipule epidermis as a result of varying protofilament monomers sizes and distance between them

Microtubules in lipotubuloids of the Ornithogalum umbellatum stipule epidermis cells change their diameters depending on the motion of the cytoplasmic domains rich in microtubules and lipid bodies. Microtubules fixed during rotary and progressive motion of the lipotubuloids composed of the same number of protofilaments fall into two populations – wide (43–58 nm) and narrow (24–39 nm) in size. Following blockage of the motion with 2,4-dinitrophenol (DNP), the range of this diversity is smaller, microtubules become a medium-sized population (34–48 nm). When DNP is removed and the motion reactivated, 2 populations of microtubules reappear. Analysis of the structure of the microtubule wall revealed that changes in the microtubule diameters resulted from varying distances between the adjacent protofilaments, and stretching and compression of tubulin subunits in the protofilaments.A supposition has been put forward that the changes in the sizes of O. umbellatum microtubule diameters: 1) are connected with the interactions between microtubules and actin microfilaments lying along these microtubules; 2) can be the driving force of the rotary motion of lipotubuloids.     

Immunogold method evidences that kinesin and myosin bind to and couple microtubules and actin filaments in lipotubuloids of Ornithogalum umbellatum ovary epidermis

Lipotubuloids in ovary epidermis of Ornithogalum umbellatum which are a domain of cytoplasm containing a lot of lipid bodies, microtubules and actin filaments, ribosomes, endoplasmic reticulum as well as scarce mitochondria, microbodies, dictyosomes, autolytic vacuoles, exhibit progressive-rotary motion. The immunogold method demonstrated that microtubules and actin filaments of lipotubuloids might be connected with one another by myosin and kinesin. It was supposed that collaboration of motor proteins with actin filaments and microtubules makes autonomic high peripheral speed rotary motion of lipotubuloids in epidermis cells possible. Moreover, myosin was also detected in Golgi bodies in lipotubuloid. In lipotubuloids, the immunogold method demonstrated immunosignals after the use of an antibody to dynein light chains but spectroscopy mass analysis showed that in O. umbellatum epidermis lacked dynein heavy chains.     

Variations in mental performance under moderate cold stress

Effects of moderate cold stress on reasoning ability, associative learning and critical flicker frequncy of Indian subjects were studied by exposing them to 25C,. 20C, 15C and 10C for three hours. A second set of experiments was also conducted to confirm the conclusions of the first by using the same temperatures and duration of exposure. However, not only the sample used in the second case was larger and different but also the mental functions tested were numerical ability, running memory and mental alertness. It has been concluded that there is a significant impairment of simple cognitive functions at 15C which is 10C lower than their most comfortable temperature of 25C.     

The effect of ambient temperature on diurnal rhythm in heat production and activity in pigs kept in groups

The effect of ambient temperature on diurnal rhythm of metabolic rate and activity was studied in group housed pigs in two trials. Two climate controlled respiration chambers were used, one for each trial. Each chamber contained two groups of 8 pigs. During the experiment of 31 days the mean live weight of the animals increased from 28 to 40 kg. Feeding level was kept constant at 93 kg^–0.75. d^–1. Feed contained 12 kJ of metabolizable energy per g. Temperature treatment started with 20C for two days. After that it was lowered in stepwise fashion by 4K to 16, 12 and 8C. Each temperature treatment lasted two days. After that temperature it was increased in steps to 20C in 8 days. The whole procedure was repeated once. Metabolic rate and activity were measured continuously during the 24 hrs of every second day of the temperature treatment.Metabolic rate increased at temperatures below 16C. Activity was associated with ambient temperature. At low temperature, the total activity related heat production was increased, especially during day time. Variation in metabolic rate within a day was not reduced by low ambient temperature. Thermal requirement, calculated as lower critical temperature, was about 14C as averaged over the day, (16.1C during day time and 13.6C during night time). Extra thermal heat production below thermoneutrality was affected by time of day and activity.     

Variations cardio-respiratoires et metaboliques à l'effort sous-maximal (P=40% Pmax) et maximal (Vita Max) en conditions thermiques froide (0‡C) et neutre (20‡C)

Resume Cette étude a pour but d'étudier les variations physiologiques et métaboliques tant au repos, qu'au cours d'efforts physiques de longue durée (2h) à 40% de la puissance maximale et d'efforts exhaustifs dans des conditions d'hypothermie ambiante (0C) en comparaison de valeurs recueillies en conditions thermiques neutres (20C). L'ensemble des épreuves furent exécutées en chambre climatique par: d'une part 11 sujets mâles pour l'effort exhaustif et d'autre part 8 sujets mâles pour l'exercice sous-maximal. Nous avons observé une légère bradycardie à 0C pour nos deux groupes à la fin de l'effort. La VO₂ et la ventilation pulmonaire sont plus élevées à 0C lors de l'effort maximal, nous observons toutefois le phénomène inverse lors de l'exercice sousmaximal. Les concentrations plasmatiques en acide lactique sons moins élevées et les bicarbonates plus élevés en ambiance thermique froide pour les deux conditions expérimentales. Le pH et la température rectale demeurent stables. Le RQ ne présente pas de différences significatives à la fin de chacun des deux efforts à 20C et 0C.

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The purpose of this study is to investigate the responses on cardiorespiratory and metabolic level measured at rest, during a long-term (2 h) submaximal exercise (P=40% Pmax) and during an exhaustive exercise (Vita Max) and recovery time in normal (20C) and in hypothermic (0C) conditions. The ergometric exercises were performed by 11 male subjects (Vita Max) and 8 male subjects (submaximal exercise) in a climatic room. We have observed a slight but mostly not significant (P<.05) bradycardia for both groups at the end of the exercise. VO₂ and pulmonary ventilation are higher at the end of the maximal exercise performed at 0C, this phenomenon is reversed for the submaximal exercise. The lactate concentrations are lower at 0C. For the same temperature the bicarbonates are higher. pH and T rect are not different in both experimental conditions and RQ is not significantly affected by temperature variations.

     

Chromosomal location of esterase,peroxidase and phosphoglucomutase isozyme structural genes in cultivated rye (Secale cereale L.)

Summary Isoelectric focusing of esterase (EST), peroxidase (PRX), and phosphoglucomutase (PGM) isozymes in Chinese Spring wheat, Imperial rye and several Chinese Spring/Imperial and Holdfast/King II addition, translocation and substitution lines revealed the chromosomal location of nine Est loci previously described and of one Prx and Pgm locus. Loci Est1, Est2, Est3, Est5, Est6 and Est7 were found on chromosome arm 5RL, Est8 and Est9 on chromosome 6R in Imperial rye, and the Est10 locus on chromosome arm 4RL in Imperial rye and King II rye. A discrepancy was found between the chromosomal location of the Prx locus in Imperial where chromosome 2R was responsible for the expression of the peroxidase enzyme, and King II with chromosome 1R carrying the Prx gene. As a possible explanation, the occurrence of translocation events during the production of wheat/rye aneuploid lines is discussed. The rye Pgm locus could be associated with chromosome 4RS in Imperial and King II rye. Except for the location of Est loci on chromosome 5RL, the results reported in this paper lend further evidence for the assumed homoeology relationships between the chromosomes of Triticinae and for the conservation of gene synteny groups during the evolution of the Triticeae tribe.     

Transport of rRNA into cytoplasm required for initiation of S phase in root meristem cells inHelianthus annuus L.

Summary Cold treatment (10C) of root meristem during a period longer than duration of the cell cycle in 20C causes a blocking of most cells in G₁. One of the causes of cell cycle blockade is the decrease of rRNA synthesis and inhibition of rRNA transport into cytoplasm. Transfer of seedlings to 20C results in increase of rRNA synthesis and its transport to cytoplasm as well as transition of almost all cells from G₁ to S during 3 hours. Synchronization of DNA replication, comprising cells within rows of cells, is preceded by similar transport patter of rRNA to cytoplasm.This work was supported by the Polish Academy of Sciences within the project 09.7.1.4.4.     

Supraoptimal growth-temperature reduces the heat-shock sensitivity of the chrysophycean flagellatePoterioochromonas malhamensis

Summary The chrysophycean flagellatePoterioochromonas malhamensis shows some characteristic alterations after a sublethal heat-shock (42 C, 16 minutes). Most cells round up and retract their cytoplasmic tail. The lorica formation is affected and, in nearly all cells, flagellar activity. Most membrane systems, especially the dictyosome, are severely damaged. In contrast the flagellar root apparatus and the cortical microtubules seem to be unaffected.After growth at a supraoptimal temperature of 33 C and a subsequent heat-shock (42 C, 16 minutes) the cells do not show the heat injuries reported above. The ability to form the lorica becomes also adapted to higher temperatures.Possible adaptation mechanisms are discussed.     

Intraspecific variation in the water relations of Salix arctica,an arctic-alpine dwarf willow

Summary The seasonal and diurnal water relations were investigated within arctic and alpine populations of the dwarf willow Salix arctica. Marked differences that were habitat dependent (e.g. xeric vs. mesic) occured both within and between the populations. The environmental variables that most affected plant water balance and the bulk tissue water relations were soil water potential (_soil) and the leafto-air water vapor pressure gradient (w), however, low soil temperature (<4.0° C) also had a marked effect in the wet to mesic habitats. The effects of declining _soil and increased w were most pronounced in the plants growing in xiric habitats in both populations. Stomatal response to increased w was two-fold greater in alpine versus arctic plants and is hypothesized to have arisen in response to more frequent exposure to the higher evaporative conditions of alpine existance. Seasonal fluctuations in the osmotic potential closely followed changes in _soil, suggesting that these were active rather that passive changes. Additionally, plants from xeric habiats had a lower bulk tissue elastic modulus (more elastic tissues) in both arctic and alpine populations. The osmotic and elastic properties enhanced turgor maintenance over a broad range of leaf water potentials and during periods when w was high. Turgor maintenance also correlated to continued transpiration despite fluctuations in soil and atmospherically induced water deficits. Arctic habitats have a shorter growing season, lower soil temperatures due to the presence of permafrost, but higher soil water potentials and lower leaf-to-air vapor pressure gradients than alpine habitats. The observed variation in patterns of stomatal conductance and in values of tissue water relations characteristics between arctic and alpine populations of S. arctica is hypothesized to have arisen in response to these different environmental regimes which represent different selective regimes that occur along the arctic-alpine environmental continuum inhabited by this wide ranging species.     

Mapping of β-glucan content and β-glucanase activity loci in barley grain and malt

Genetic study of -glucan content and -glucanase activity has been facilitated by recent developments in quantitative trait loci (QTL) analysis. QTL for barley and malt -glucan content and for green and finished malt -glucanase activity were mapped using a 123-point molecular marker linkage map from the cross of Steptoe/Morex. Three QTL for barley -glucan, 6 QTL for malt -glucan, 3 QTL for -glucanase in green malt and 5 QTL for -glucanase in finished malt were detected by interval mapping procedures. The QTL with the largest effects on barley -glucan, malt glucan, green malt -glucanase and finished malt glucanase were identified on chromosomes 2,1,4 and 7, respectively. A genome map-based approach allows for dissection of relationships among barley and malt glucan content, green and finished malt -glucanase activity, and other malting quality parameters.     

Spectroscopy of non-photochemical and photochemical quenching of chlorophyll fluorescence in leaves; evidence for a role of the light harvesting complex of Photosystem II in the regulation of energy dissipation

Dissipation of absorbed excitation energy as heat, measured by its effect on the quenching of chlorophyll fluorescence, is induced under conditions of excess light in order to protect the photosynthetic apparatus of plants from light-dependent damage. The spectral characteristics of this quenching have been compared to that due to photochemistry in the Photosystem II reaction centre using leaves of Guzmania monostachia. This was achieved by making measurements at 77K when fluorescence emission bands from each type of chlorophyll protein complex can be distinguished. It was demonstrated that photochemistry and non-photochemical dissipation preferentially quench different emission bands and therefore occur by dissimilar mechanisms at separate sites. It was found that photochemistry was associated with a preferential quenching of emission at 688 nm whereas the spectrum for rapidly reversible non-photochemical quenching had maxima at 683 nm and 698 nm, suggesting selective quenching of the bands originating from the light harvesting complexes of Photosystem II. Further evidence that this was occurring in the light harvesting system was obtained from the fluorescence excitation spectra recorded in the quenched and relaxed states.Abbreviations pH transthylakoid pH gradient - F_o minimum level of chlorophyll fluorescence when Photosystem II reaction centres are open - F_m maximum level of fluorescence when Photosystem II reaction centres are closed - F_v variable fluorescence F_m minus F_o - F'_o F_o in any quenched state - F_m F_m in any quenched state - LHCII light harvesting complexes of Photosystem II - PSI Photosystem I - PS II Photosystem II - qN non-photochemical quenching of chlorophyll fluorescence - qE non-photochemical quenching of chlorophyll fluorescence that occurs in the presence of a pH     

Detrimental effects of high ambient temperature on fertility and early embryo survival in sheep

Percent of ova fertilized was significantly (P<0.01)lower in ewes exposed to 32C temperature on the twelfth day of the cycle before breeding (40.7.% vs 94.2% for controls). The average rectal temperature of the ewes was increased 1.7C within 24 hr after exposure to the elevated temperature. Morphologically abnormal ova were increased from 3.8% in control ewes to 55.6% in treated ewes. In ewes exposed to the 32C one day after breeding all ova were cleaved,but 30.8% were morphologically abnormal. In control ewes 87.5% lambed,but none of the ewes exposed to 32C before or at time of breeding lambed. In ewes exposed to 32C at 1, 3,5 or 8 days after breeding, 20%, 35%, 40% and 70%, respectively, lambed.Embryo mortality was significantly (P<0.01) higher for all treated ewes except those in the 8-day group.The sheep zygote is most sensitive to the harmful effects of high ambient temperature during the initial stages of cleavage before it enters the uterus.

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Zusammenfassung Die Zahl befruchteter Eier von Schafen, die vor dem Decken am 12. Tage des Zyklus einer Temperatur von 32C exponiert wurden, war signifikant niedriger(40,7%)als bei Kontrolltieren (94,2%) 24 Stunden nach übergang in die höhere Temperatur war die Rektaltemperatur 1,7C höher als vorher.Der Anteil morphologisch abnormaler Eier bei den Kontrollen betrug 3,8%, bei den exponierten Tieren 55,6%. Bei Tieren,die einen Tag nach dem Decken 32C exponiert wurden, zeigten alle Eier Teilung,doch davon waren 30,8% morphologisch abnormal. Von den exponierten Tieren lammte keines, von den Kontrolltieren 87,5%. Von Schafen, die 1, 3, 5 oder 8 Tage nach dem Decken 32C exponiert wurden, trugen 20, 35, 40 und 70% aus. In allen exponierten Gruppen war die MortalitÄt signifikant höher (P<0,01) — ausser in der 8-Tage Gruppe — als bei Kontrollen. Die Zygote des Schafes ist Äusserst empfindlich gegen hohe Temperatur wÄhrend der Initialstadien der Teilung, ehe sie in den Uterus gelangt.

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Resume La proportion d'ovules fécondés a été trouvée significativement moindre (P<0,01) chez des brebis exposées à une température de 32C lors du 12ème jour du cycle précédant l'insémination que chez des animaux-témoins (40,7% contre 94,2%).Pendant les 24 heures consécutives à l'exposition à la chaleur, la température rectale des brebis dépassait de 1,7C sa valeur au cours de la période précédente.La proportion d'ovules morphologiquement anormaux était de 3,8% chez les animaux-témoins contre 55,6% chez les animaux exposés à la chaleur. Chez des animaux qui avaient été exposés à une température de 32C le lendemain de l'insémination, tous les oeufs étaient segmentés, pourtant 30,8% d'entre eux présentaient des anomalies morphologiques.Desbrebis ainsi exposées, aucune n'a conduit sa gestation à terme alors que 87,5% des animaux-témoins ont agnelé. Des brebis exposées à la chaleur 1, 3, 5 ou 8 jours après l'insémination, respectivement 20, 35, 40 et 70% ont mené leur gestation à terme. Dans tous les groupes exposés, la mortalité embryonnaire a été significativement plus élevée (P<0,01) que chez les témoins, à l'exception toutefois du groupe exposé 8 jours après l'insémination. Dans l'espèce ovine, le produit de la fécondation est très sensible à 1'hyperthermie pendant les premiers stades de la segmentation qui précèdent son entrée dans l'utérus.

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The investigation reported in this paper is in connection with a project of the Kentucky Agricultural Experiment Station and is published with the approval of the Director.     

Effect of protons and cations on chloroplast membranes as visualized by the bound ANS fluorescence

Structural changes in the chloroplast membranes caused by acidification and heat-treatment are studied by observing the changes in the fluorescence of ANS bound to thylakoid membranes. On addition of acids to buffered suspension of isolated pea chloroplasts, the fluorescence intensity of bound ANS shows a sigmoidal rise on reaching a pH value of about 4.5. A part of the fluorescence enhancement of bound ANS brought about by protons is not reversible on back titration with alkali. The reversible part of acid induced rise in ANS fluorescence possibly reflects structural changes expected to be associated with photophosphorylation. Divalent cations enhance the fluorescence of ANS bound to chloroplasts between a pH range 4.5–7.0 but diminish it if the pH is below 4.5.Addition of acid to heat-treated chloroplasts shows similar sigmoidal rise in ANS fluorescence intensity on lowering the pH to about 4.5. On addition of acid upto a pH of 3.1, the ANS fluorescence is greater than that of untreated chloroplasts, however, at pH below 3.1, the fluorescence of bound ANS is lower than the control chloroplasts. This observation indicates that heat-treatment caused some alteration of the microstructure of thylakoid membranes of chloroplasts besides the usual loss in the O₂ evolving capacity.This is further confirmed from the studies of Hill-activity and ANS binding to chloroplasts incubated at various temperatures in the absence and presence of aliphatic alcohol. Hill-activity (DCPIP reduction) of chloroplasts incubated at temperatures between 25 C and 55 C first increases reaching a maximum at 45 C and then declines rather sharply, when the chloroplasts are heated beyond 45 C (Tmax). The presence of 200 mM n-butyl alcohol or 40 mM n-amyl alcohol during the warming treatment lowers the temperature by 8 C at which the decline in the Hill-activity is observed. An enhancement in the fluorescence intensity and a blue shift of the emission spectrum of bound ANS are noted if the chloroplasts are heated beyond the Tmax either in absence or presence of alcohol. The changes in the fluorescence of ANS bound to heat-treated chloroplasts plausibly reflect the nature of the structural changes in chloroplasts during the heating upto 55 C.Abbreviations ANS 1-anilino-8-naphthalene sulphonate - DCPIP 2,6-dichlorophenol indophenol     

Thermal stability of soluble mitochondrial H+-ATPase

ATPase melting has been studied by circular dichroism and differential scanning microcalorimetry. Decomposition of the -helix of H⁺-ATPase (in which about 80% of the peptide groups of the enzyme are involved) following thermal treatment is shown to proceed gradually, beginning with room temperature. Effect of nucleotides upon melting is detected in the range of 20–40 C. Above 40 C, the pattern of thermal decomposition of the three-dimensional structure of H⁺-ATPase is independent of the nature of nucleotides present. Highly stable -helical sites have been found in the enzyme molecule. Possible mechanism of formation of such sites is discussed, and the results obtained are compared with data on thermal stability of ATPase from thermophilic bacteria. Structural changes in the molecule following thermal treatment are compared with ATPase activity changes under similar experimental conditions.     

Replicon fusion mediated by a single-ended derivative of transposon Tn1721

Summary Tn17221K, a derivative of transposon Tn1721 lacking one terminal inverted repeat (IR) and conferring kanamycin resistance, promotes transposition of the resistance marker to a target replicon at about 100-fold lower frequency than the wild-type element. A study involving restriction analysis of 16 independent Tn17221K-mediated events led to the following results: (i) Tn17221K mediates fusions of the donor (pRU506) and target (RSF1010) replicons; the fused entities are non-permuted. (ii) Tn17221K promotes insertions of donor DNA at many different sites in the target replicon. (iii) The analyzed fusion plasmids contain the entire target and various lengths of donor DNA. Eleven products contain the entire donor plasmid plus a duplication of the IR (class A), whereas five products contain only portions adjacent to the single IR (class B). (iv) In each case the two replicons are joined at (or very close to) the single IR. The second junction is located shortly beyond the duplicated IR in class A and at different sites within the donor plasmid in class B. These results are interpreted in terms of asymmetric replicative transposition.     

Colchicine and microfibril orientation

Summary Investigations on the mechanism of orientation of the cellulose microfibrils of the green algaOocystis solitaria have been carried out. This organism demonstrates easily observable and highly ordered microfibrils in its wall, which are arranged parallel to one another and regularly alternate at 90 from layer to layer of which there are approximately 30. During the entire wall development, and always parallel to one of the microfibril directions, are microtubules lying in the cortical cytoplasm. In the presence of 10^–2 M colchicine, microtubules are no longer detected and the typical cell wall pattern is not developed. The possible role of microtubules in the orientation of cellulose microfibrils is briefly discussed.     

Growth temperature acclimation byAmoeba proteus: Effects on cytoplasmic organelle morphology

Summary The effects on subcellular morphology of maintaining amoebae at temperatures other than 20 C (the routine culture temperature) were assessed. Estimations of cycling potential at each temperature confirmed that acclimation had affected gross cell functioning. Generation times ranged from no division at 6 C, to an optimal minimum of 2 days at 22 C.Organelle morphology changes were studied after 5 days of growth at the new temperatures; alterations were most evident at the extremes of 6 and 28 C. The main mitochondrial alteration resulted in changes to the ratio of Type I: Type II organelles; with a decrease in Type I forms away from the optimal range of 20–22 C. Extended culturing at 6 C generated mitochondrial matrical inclusions. Ribosomal attachment to the endoplasmic reticulum, a common feature of 20 C-grown cells, decreased at the temperature extremes, where an increase in free ribosomes occurred. Upon extended culture at 6 C helical structures, usually observed in groups only within the nucleus, were also present in the cytoplasm. Golgi complexes were less common in cells maintained at extreme temperatures and often showed differences in shape. These changes were all reversible on a return to culturing at 20 C.The possible functional significance of these findings is discussed.     

Effects of hyperthermia on enzymes and electrolytes in blood and cerebrospinal fluid in dogs

The effects of exposure to various degrees of heat stress on serum glutamate—oxaloacetate transaminase (SGOT), serum glutamate-pyruvate transaminase (SGPT), alkaline phosphatase (ALK-P-ase), calcium and chlorides have been studied on 75 dogs. Rectal temperature (T_re) was recorded before and after exposure to heat stress. These dogs were divided into 5 groups, according to the T_re level attained after exposure to heat stress. Rectal temperature was raised from normal to 39.45±0.47C in the first group, to 40.93±0.17C in the second group, to 41.87±0.22C in the third group, to 42.90 ± 0.21C in the fourth group and to 43.93±0.19C in the fifth group. The concentration of enzymes SGOT, SGPT and ALK-P-ase in blood and cerebrospinal fluid (CSF) increased significantly with hyperthermia. Calcium and chlorides concentrations in blood and in CSF tended to increase in hyperthermia. The integrity of the blood brain barrier for these enzymes and calcium is maintained under mild hyperthermia but it breaks down partially under influence of more severe hyperthermia. Core temperature above 41C results in damage to tissues and consequential rise of plasma enzymes. This degree of hyperthermia also seems to mark the beginning of injury to blood brain barrier. Critical core temperature tolerated by 50% of animals was 44C.     

Use of foliar <Superscript>15</Superscript>N and <Superscript>13</Superscript>C abundance to evaluate effects of microbiotic crust on nitrogen and water utilization in <Emphasis Type="Italic">Pinus massoniana</Emphasis> in deteriorated pine stands of south China

We compared the foliar ¹⁵N and ¹³C values of Pinus massoniana growing on soils with and without microbiotic crust to examine the influence of the microbiotic crust on N and water use in plants in deteriorated watersheds in southern China. At our study site, litterfall and undergrowth had been intensively removed for fuel and soil N concentration was extremely low. Microbiotic crust covered the lower slope within the watersheds and pine trees were taller here than on the middle and upper slopes, although the crust reduced the amount of rainfall that could penetrate the soil. The foliar ¹⁵N values were greater (closer to zero) in pine trees growing on soil covered with microbiotic crust on the lower slope than on the middle and upper slopes, which lacked the microbiotic crust. These data suggest that P.massoniana may depend on N fixed by the microbiotic crust on the lower slope, and on N carried by precipitation on the middle and upper slopes. The microbiotic crust did not influence foliar ¹³C, an index for water use efficiency, in P.massoniana. The fact that P.massoniana biomass was greater on the lower slope, which is less permeable to rainfall, suggests that P.massoniana growth may be limited by the amount of available N rather than by water. The microbiotic crust may improve plant productivity by increasing N availability, despite its negative effect on water availability.     

Physiological characteristics of cold acclimatization in man

Studies were conducted on 15 healthy young soldiers to evaluate the effect of a cold acclimatization schedule on the thermoregulatory and metabolic activity on exposure to acute cold stress. These men were exposed to cold (10C) for 4 h daily wearing only shorts for 21 days, in a cold chamber. They were subjected to a standard cold test at 10 ± 1C the day 1, 6, 11 and 21. The subjects were made to relax in a thermoneutral room (26–28C) for 1 h and their heart rate, blood pressure, oxygen consumption, oral temperature, mean skin temperature, mean body temperature, peripheral temperatures, and shivering activity were recorded. Then they were exposed to 10C and measurements were repeated at 30 min intervals, for 2 h. The cold induced vasodilatation (CIVD), cold pressor response and thermoregulatory efficiency tests were measured initially and at the end of acclimatization schedule. The data show that the procedure resulted in elevated resting metabolism, less fall in body temperature during acute cold stress, reduction in shivering, improvement in CIVD and thermoregulatory efficiency and less rise in BP and HR during cold pressor response. The data suggest the possibility of cold acclimatization in man by repeated exposure to moderately severe cold stress.