The relative influence of urban climates on outdoor human energy budgets and skin temperature II. Man in an urban environment

Four typical urban neighborhoods or street canyon settings (including street parks) were simulated. These urban morphologies were exposed to typical summer and winter climatic scenarios for latitudes 10, 34, and 50N. The changes induced in the components of the human energy budget were examined. Resultant skin temperatures were compared with non-urban, unobstructed environments.     

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.     

The North Sea: source or sink for nitrogen and phosphorus to the Atlantic Ocean?

Annual nitrogen and phosphorus budgets for the whole North Sea taking into account the most recent data available were established. The area considered has a total surface of approximately 700,000km² and corresponds to the definition by OSPARCOM (Oslo and Paris Commission) with the exclusion of the Skagerrak and Kattegat areas. Input and output fluxes were determined at the marine, atmospheric, sediment and continental boundaries, and riverine inputs based on river flows and nutrient concentrations at the river–estuary interface were corrected for possible estuarine retention. The results showed that the North Sea is an extremely complex system subjected to large inter-annual variability of marine water circulation and freshwater land run-off. Consequently, resulting total N (TN) and P (TP) fluxes are extremely variable from 1 year to another and this has an important influence on the budget of these elements. Total inputs to the North Sea are 8870±4860kTNyear^–1 and 494±279kTPyear^–1. Denitrification is responsible for the loss of 23±7% of the TN inputs while sediment burial is responsible for the retention of only of 2±2% of the TP input. For TN, due to the large variability on marine and estuarine fluxes, and to the uncertainty related to the denitrification rate, it was concluded that the North Sea could either be a source (1930kTNyear^–1) or a sink (1700kTNyear^–1) for the waters of the North Atlantic Ocean. For TP it was concluded that the North Sea is mostly a source (–4 to 52kTPyear^–1) for the waters of the North Atlantic Ocean.     

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.     

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.     

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.     

Heterogeneity of epithelial cells in the human thymus

Summary To evaluate interrelationships among epithelial cells, and between morphology and function in the microenvironment, we studied the ultrastructural morphology of epithelial cells in sections of human thymus from donors aged 2 months to 31 years. Six types of epithelial cells were observed: subcapsular-perivascular (type 1); pale (type 2); intermediate (type 3); dark (type 4); undifferentiated (type 5); and large-medullary (type 6). Cells of types 2, 3 and 4 were found throughout the organ. The type-2 to -4 epithelial cells may represent various stages in a differentiation process. In this, type-2 cells are very active and type-4 cells are possibly degenerating elements. Type-4 cells can also contribute to Hassall's corpuscles. Type-5 cells were located mainly in the cortico-medullary region and showed the morphological characteristics of undifferentiated elements. Type-6 cells were located exclusively in the medulla and displayed characteristics of cellular activity. Small Hassall's corpuscles consisted of type-6 epithelial cells; in larger corpuscles many nuclei of type-6 cells were found. Cells of types 2 and 6 contained tubular structures (diameter approximately 20 nm).Concerning the function of thymus epithelial cells, the features associated with protein synthesis observed in cellular types 2 and 6 make them likely candidates for humoral factor-producing and/or secreting elements. In addition, type-2 and -3 cells in the cortex appear to contribute to a special pattern of epithelium-lymphocyte interaction (thymic nurse cells), as demonstrated by the intracytoplasmic location of lymphocytes in the epithelial cells. The various steps in intrathymic T-cell maturation occur at locations in a microenvironment composed of morphologically distinct epithelial cells.     

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.     

Frostbite and the significance of a temperature-sensation scale in field and laboratory conditions

The literature indicates that rapid thawing in water between 42 and 45C provides the best prognosis for frostbitten limbs.A temperature:sensation scale for the normal hand was derived and tested in laboratory and field conditions. The scale permitted the preparation of water suitable for frostbite treatment by the majority of subjects without access to a thermometer. The maximum observed inaccuracy was 1.2C outside the preferred range but was well withing the safe range for treatment.

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Zusammenfassung Die beste Prognose zur Behandlung von Erfrierungen bietet nach den Erfahrungen in der Literatur das schnelle Auftauen von erfrorenen Gliedern bei Wassertemperaturen von 42–45C. Für die gesunde Hand wurde eine Temperatur-Wahrnehmungsskala aufgestellt und unter verschiedenen Bedingungen im Laboratorium und im Freien geprüft. Ohne Zugang zu einem Thermometer gestattete die Skala in der Mehrzahl der FÄlle die ErwÄrmung von Wasser auf Temperaturen, die für die Behandlung von Erfrierungen geeignet sind. Die grösste Ungenauigkeit zwischen SchÄtzwert und Thermometerwert war 1.2C ausserhalb des gewünschten aber noch innerhalb des für die Behandlung zulÄssigen Bereiches.

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Résumé D'après les indications de plusieurs auteurs, le meilleur traitement de membres gelés consiste à les dégeler dans de l'eau à une temperature entre 42 et 45C. Une échelle température-sensation pour la main normale a été mise au point et vérifiée au laboratoire ainsi qu'en plain air.Cette méthode a permis la préparation d'eau en vue d'un traitement de gelures sans faire usage d'un thermomètre dans la plupart des cas. L'erreur maximum observée était de 1,2 C sans que les limites de l'intervalle propice à un traitement ne soient jamais dépassées.

     

Prediction of the beginning of the olive full pollen season in south-west Spain

Given the clinical and agricultural importance of the olive in SW Spain, we have carried out a study to predict the starting date of its full pollen season. The study covers 6 years of meteorological and palynological observations — the latter using a Cour sampler installed in Huelva (SW Spain). The results obtained show that olive full pollination begins when the plant has accumulated 731C of daily temperature above 5C from the end of its dormant period. The mean duration of this accumulation was 83 days. A positive relationship has been found between mean temperature of the months before the pollen season (February and March) and the date when the season starts (April). From the data available, rainfall registered between 1 September and 31 March (both before pollination), does not affect the starting date of the full pollen season, but can affect total pollen production, particularly in years with prolonged drought.     

Temperature dependent structural changes of intraphage T7 DNA

The phenomena connected with the first phase transition step of the native T7 phage at 40C–65 C have been studied using various methods. In this temperature range a) the optical melting curve shows an absorption decrease, b) the maximum of the small-angle X-ray scattering characteristic for DNA packing disappears, c) there is a drop of biological activity and d) there are changes in the structure of the difference absorption spectra of native phages versus isolated DNA. All data are interpreted assuming a structural change of the DNA due to the release of its protein coat towards the end of the first phase transition step (at 60–65 C in the case of M9 buffer). Above this temperature the intraphage DNA packing appears to be destroyed and the DNA structure seems to be similar to that in DNA solution.     

High-resolution autoradiography of nuclear modifications during and after heat treatment ofNeurospora crassa

Summary The appearance of perinucleolar electron-dense spots in the nuclei of macroconidia ofNeurospora crassa incubated at 46C and their disaggregation after shift-down to 25 C have been investigated by high-resolution autoradiography after (5-³H) uridine pulses with or without chase periods. The RNA of these ribonucleoprotein-rich dense spots has been found to originate mainly from the heatsensitive nucleolus; after return to 25 C, the nucleolar activity was recovered and the RNA material stored either in an unprocessed or a mature rRNA form in the dense spots was found to be progressively extruded into the cytoplasm.     

Thermoregulation and thermal perception in the cold and heat before and after intermittent heat adaptation

Students wearing swim suits were exposed for 30 min to neutral room temperature (T_R=28C). During the following 60 min they were subjected to gradual decreases or increases of room temperature reaching 12C or 45C, respectively. Static thermal stimuli were applied to the palms of the right (38C) and left (25C) hands. Hands and feet of all subjects were thermally isolated at 22C ambient temperature. General thermal comfort (GTC), local thermal comfort (LTC), skin blood flow (which is proportional to heat transport index ) several body temperatures, oxygen-consumption , and sweat rate (S), were measured. After moderate intermittent heat exposures (7 times for 1h at T_R=42.5C) the experiments started again. From GTC, LTC, or as functions of T_R, no new knowledge about thermoregulatory or adaptive mechanisms was available. The high in the cold stimulated left hand, however, and the oscillatory thresholds (_OSC) for rhythmic vasomotion indicated the peripheral influence of skin temperature, as well as local, mean skin temperature (¯T_s) and core temperature. When exposed to moderate temperature decreases or increases the body seems to react only with increasing thermal resistance by vasoconstriction or an increase of sweat rate, respectively. Moderate heat adaptation is only able to raise sweat rate, but not the thresholds and gain of the S-function. We assume that functional studies of adaptive modifications in humans must be conducted at temperatures greatly beyond those used in these experiments.     

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.

     

Effects of fasting on maximum thermogenesis in temperature-acclimated rats

To further investigate the limiting effect of substrates on maximum thermogenesis in acute cold exposure, the present study examined the prevalence of this effect at different thermogenic capabilities consequent to cold- or warm-acclimation. Male Sprague-Dawley rats (n=11) were acclimated to 6, 16 and 26C, in succession, their thermogenic capabilities after each acclimation temperature were measured under helium-oxygen (21% oxygen, balance helium) at –10C after overnight fasting or feeding. Regardless of feeding conditions, both maximum and total heat production were significantly greater in 6>16>26C-acclimated conditions. In the fed state, the total heat production was significantly greater than that in the fasted state at all acclimating temperatures but the maximum thermogenesis was significant greater only in the 6 and 16C-acclimated states. The results indicate that the limiting effect of substrates on maximum and total thermogenesis is independent of the magnitude of thermogenic capability, suggesting a substrate-dependent component in restricting the effective expression of existing aerobic metabolic capability even under severe stress.     

Rhodopsin phosphorylation occurs at metarhodopsin II level

Photolyzed rhodopsin was phosphorylated in bovine rod outer segments incubated at –10 C. In the experiment in which urea-treated outer segments and rhodopsin kinase were incubated with ATP in the presence of 30% glycerol, the extent of phosphate incorporation at –10 C was about 30% of that at 37 C. Separation of phosphorylated rhodopsin by isoelectric focusing indicated that a limited number of sites were phosphorylated at –10 C. The partially phosphorylated pigment incorporated more phosphates when the temperatures was raised to 37 C. This was partly due to decreased inhibition of phosphorylation by glycerol at higher temperature. Since the maximum phosphorylation at –10 C (at which metarhodopsin II is stable) occurred at a pH value (6.0) lower than the pKa for metarhodopsin I-metarhodopsin II transition, metarhodopsin II was suggested to be the preferred substrate for rhodopsin kinase at –10 C. Limited proteolysis with thermolysin of rhodopsin phosphorylated at 37 C released peptides containing about 50% of the total phosphate incorporated. In contrast, proteolytic digestion of rhodopsin phosphorylated at –10 C released negligible amounts of phosphate-containing peptides. The results were taken to suggest that the incorporation of phosphates at metarhodopsin II level under the present condition occurred in the residues other than those removed by thermolysin digestion.Based on material presented at the Fifth International Congress of Eye Research, Eindhoven, October 1982     

Extracellular amylolytic system of the yeast Lipomyces kononenkoae

Summary A strain of the yeast Lipomyces kononenkoae which converted starch into SCP with a high yield, produced three extracellular amylases which were purified from the culture fluid by Ficoll concentration, dialysis, isopropanol precipitation and DE-cellulose chromatography: an -amylase, a glucoamylase and a debranching transferase. The latter transferred -1,6-glucosyl units from panose to glucose forming maltose and appeared to have some debranching activity on amylopectin. The -amylase had the following properties: MW 38000 daltons; no effect of added calcium ions on activity; optimum temperature and pH for activity around 40°C and pH 5.5; H and S of heat inactivation 24360 cal mol^–1 and 29.2 cal deg^–1 mol^–1; range of pH stability pH 4–6.5; pI=7.1; final low molecular weight products of starch hydrolysis, maltose and glucose; K_m (40°C, pH 5.5) for starch 2.7 gl^–1, for maltotriose 109 gl^–1; uncompetitive inhibition by maltose with K_i (40°C, pH 5.5) 29.5 gl^–1. The glucoamylase had the following properties: MW 81500 daltons; optimum temperature and pH for activity around 50°C and pH 4.5: H and S of heat inactivation 20400 cal mol^–1 and 17.7 cal deg^–1 mol^–1; range of pH stability pH 4–6.5; pI=6.1; K_m (30°C, pH 4.5) for soluble starch 16.2 gl^–1, for maltose 0.36 gl^–1, for p-nitrophenyl--D-glucoside 0.35 gl^–1; competitive inhibition by glucose with K_i (30°C, pH 4.5) 4.7 gl^–1.     

On the rise time of the R1-component of the “Early receptor potential...: Evidence for a fast light-induced charge separation in rhodopsin

The rising phase of the R₁-component of the early receptor potential from isolated cattle retinas was measured with high time resolution. When the measuring capacitance was 133 pF, a latency of about 200 ns was observed. A rise time of about 0.8 s at 0 C and 1.6 s at 37 C (extrapolated to ideal measuring conditions) was found. The negative temperature dependence indicates that the rise is not directly related to the production and decay of photolysis products of rhodopsin since the latter have positive temperature coefficients. An increase of the external measuring capacitance caused a slower rise time. The analysis of this effect allowed the determination of the source impedance of the R₁-component. The experimental results can be described with a model in which it is assumed that a fast charge separation (ns or ps) takes place in the outer segment of a photoreceptor cell, and spreads passively to the inner segment via the resistance of the interconnecting cilium. The inner relaxation could be circumvented by using isolated rod outer segments which lack the passive inner segments, i.e., a rise time of 90 ns could be measured when isolated rod outer segments were attached to Millipore filters. The results suggest that the molecular event leading to the R₁-component is an early charge separation which may be as fast as the cis-trans isomerization of the retinal chromophore.     

Surface charge density estimation by 9-aminoacridine fluorescence titration: improvements and limitations

A large number of surface charge density () and surface potential (_o) estimations have been based on 1) titrations of the fluorescence of 9-aminoacridine released from the diffuse double layer adjacent to negatively charged membrane surfaces by non-adsorbing monovalent and divalent cations, and 2) calculations using experimental data from the titration curves and the Gouy-Chapman theory of the diffuse double layer. In this paper we discuss the different simplifying approximations employed in the earlier calculations and recommend modified formulas for the calculations. The latter have been derived without any simplifying approximation concerning the ionic (electrolyte) composition of the titration assays. We also show that depends, to some extent, on the concentrations of buffer and vesicles in the assays and present experimental evidence that decamethonium (decane-1,10-bis-trimethylammonium), a bulky organic divalent cation, can be satisfactorily used for the estimation of under well-defined conditions, despite its putative interaction with membranes.Abbreviations 9-AA 9-aminoacridine - (DeM)²⁺ decamethonium - (DiM)²⁺ dimethonium - EDTA ethylenediaminetetraacetic acid - EGTA ethylene glyol-bis(-aminoethyl ether) N,N,N,N-tetraacetic acid - (HeM)²⁺ hexamethonium - MES 2-(N-morpholino) ethanesulfonic acid - MOPS 4-morpholinopropanesulfonic acid - PM plasma membrane - Tris tris(hydroxymethyl)aminomethane - surface charge density - _o surface potential Correspondence to: A. Bérczi     

Evidence for a double-helically coiled toroidal chromonema in the dinoflagellate chromosome

The structure of the dinoflagellate chromosome is examined using spread whole mounts and serial sectioning. Evidence is presented that the chromosome is composed of a toroidal bundle of DNA strands which is coiled plectonemically into a tight double helix. This structure is apparent in interphase whole-mount chromosomes and by careful analysis of serial sectioning can be shown in all mitotic stages. It is particularly apparent in the arms of replicating Y shaped chromosomes which often uncoil slightly (either naturally or as a result of the fixation used). A model is presented which is based on these results and recent genetic and biochemical data.