Activity and oxygen consumption during hypoxic exposure in high altitude and lowland sceloporine lizards

Summary Resting rates of O₂ consumption against , exercise endurance times and during recovery from vigorous exercise were measured inSceloporus occidentalis captured near sea level and inS. graciosus captured above 2850 m. Oxygen consumption against was also measured inS. occidentalis captured above 2850 m. When was recorded continuously, as ambient was slowly reduced from 155 Torr, it became directly dependent upon ambient between 110 and 120 Torr. The critical for the high altitude lizards was lower than that for the lowland lizards, which enabled the former to maintain relatively higher 's when ambient was reduced below 120 Torr. The high altitude lizards also had significantly greater endurance when stimulated to exercise at 1600 m ( 130 Torr). Both the higher under hypoxia and the greater endurance roughly parallel a significantly greater maximum in the high altitude lizards. At a simulated altitude of 3600 m ( 100 Torr), maximum and rate of recovery of the O₂ debt calculated from post active were significantly reduced in the lowland but not the high altitude lizards. The effects of simulated altitude conditions on the lowland but not the mountaine animals indicate adaptations to altitude in these sceloporine lizards. We did not find any consistent relationship between organ/body weight ratios or hematocrit and our measures of endurance or the altitude at which the lizards were captured.     

A new technique for continuous measurement of the heat of fermentation

Summary A special temperature control system has been developed and applied to continuous measuring of the heat evolved during a fermentation process. In this system, the fermentation broth was overcooled by a given constant cooling water flow. The excess heat removed from the fermentor was then made up by an immersion electrical heater. The action of the temperature controller was precisely monitored as it varied in response to the amount of heat produced by the microbial activities.The technique was used for determining the heat evolution byEscherichia coli grown on glucose. The ratio between quantities of total heat release and total oxygen consumption has been determined to be 0.556 MJ/mol O₂.The newly developed technique can be employed as an online sensor to monitor the microbial activities of either aerobic or anaerobic fermentation systems.Symbols C_c Heat capacity of cooling water (MJ/kg · °C) - C_p Heat capacity (MJ/kg · °C) - I Current of immersion heater (A) - K Constant in Equation (2) (h) - K Constant in Equation (13) (m³ · h · °C/MJ) - Q_c Flow rate of cooling water (m³/h) - Heat of agitation (MJ/m³ · h) - Heat dissipated by the bubbling gas (MJ/m³ · h) - Heat removal by the action of controller (MJ/m³ · h) - Heat of fermentation (MJ/m³ · h) - Heat loss to the surroundings (MJ/m³ · h) - Q_pass Constant average power dissipated by the immersion heater (MJ/m³ · h) - Fluctuating power dissipated by the immersion heater (MJ/m³ · h) - Power dissipated by the immersion heater (MJ/m³ · h) - T Temperature of fermentation broth (°C) - Constant average temperature of fermentation broth (°C) - Fluctuating temperature of fermentation broth (°C) - T_a Temperature of the ambient air (°C) - T_c Inlet temperature of cooling water (°C) - U₁A₁ Specific heat transfer coefficient for determination of heat loss to the surroundings (MJ/m³ · h · °C) - U₂A₂ Specific heat transfer coefficient for cooling surfaces (MJ/m³ · h · °C) - U₃A₃ Constant in Equation (16) (MJ/m³ · h · °C) - V Voltage of immersion heater (V) - V_L Liquid volume (m³) - OUR Oxygen uptake rate (mol O₂/m³ · h) Greek Letters H_fo The ratio between the total heat release and the total oxygen uptake (MJ/mol O₂) - _c Density of cooling water (kg/m³) - Time constant defined in Equation (6) (h) - _iM_iC_pi Heat capacity of system components (fermentation broth + fermentor jar + stainless steel) (MJ/m³ · °C)     

The relationship between the energetic efficiency in different micro-organisms and the rate and type of metabolite overproduced

Summary Data regarding the degree of energy conservation as determined by the and the highest rates of metabolite production reported for various micro-organisms have been collated and analysed. The results have indicated that the highest rates of metabolite production occur in micro-organisms possessing low efficiencies of energy conservation. Moreover, in the case of exopolysaccharide production the oxidation state of the polymer is inversely related to the value of the producing organism. In general, the rate of ATP turnover associated with exopolysaccharide production or the potential rate associated with over-production of other metabolites is inversely related to the value of the producing organism. Analysis of current production rates for a range of metabolites suggests that there is scope for major improvements of existing processes by careful selection of appropriate micro-organisms.     

A method for determining the maximal steady state of blood lactate concentration from two levels of submaximal exercise

The aim of this study was to estimate the characteristic exercise intensity _CL which produces the maximal steady state of blood lactate concentration (MLSS) from submaximal intensities of 20 min carried out on the same day and separated by 40 min. Ten fit male adults [maximal oxygen uptake _max 62 (SD 7) ml · min^–1 · kg^–1] exercisOed for two 30-min periods on a cycle ergometer at 67% (test 1.1) and 82% of _max (test 1.2) separated by 40 min. They exercised 4 days later for 30 min at 82% of _max without prior exercise (test 2). Blood lactate was collected for determination of lactic acid concentration every 5 min and heart rate and O₂ uptake were measured every 30 s. There were no significant differences at the 5th, 10th, 15th, 20th, 25th, or 30th min between , lactacidaemia, and heart rate during tests 1.2 and 2. Moreover, we compared the exercise intensities _CL which produced the MLSS obtained during tests 1.1 and 1.2 or during tests 1.1 and 2 calculated from differential values of lactic acid blood concentration ([1a^–]_b) between the 30th and the 5th min or between the 20th and the 5th min. There was no significant difference between the different values of _CL [68 (SD 9), 71 (SD 7), 73 (SD 6),71 (SD 11) % of _max (ANOVA test,P<0.05). Four subjects ran for 60 min at their _CL determined from periods performed on the same day (test 1.1 and 1.2) and the difference between the [la^–]_b at 5 min and at 20 min ( ([la^–]_b)) was computed. The [la^–]_b remained constant during exercise and ranged from 2.2 to 6.7 mmol · l^–1 [mean value equal to 3.9 (SD 1) mmol · l^–1]. These data suggest that the _CL protocol did not overestimate the exercise intensity corresponding to the maximal fractional utilization of _max at MLSS. For half of the subjects the _CL was very close to the higher stage (82% of _max where an accumulation of lactate in the blood with time was observed. It can be hypothesized that _CL was very close to the real MLSS considering the level of accuracy of [la^–]_b measurement. This study showed that exercise at only two intensities, performed at 65% and 80% of _max and separated by 40 min of complete rest, can be used to determine the intensity yielding a steady state of [la^–1]_b near the real MLSS workload value.     

Contribution to the genetics of serum β-lipoproteins in man

Summary The genetic behaviour of a human serum -lipoprotein factor, called Ag(a₁), was studied by agar micro-diffusion technique, utilizing an antibody detected in the serum from a transfused thalassemia patient. It behaves as an inherited, dominant, autosomal character, with complete penetrance at birth. It is controlled by a gene and is closely linked to the Ag ^x and Ag ^y genes.The existence of a gene Ag ^b , allelic to , is postulated but the Ag(b) antigen has not so far been detected by specific antisera.The frequency of the gene in a Milan population was found to be 0,43, and in a Berne population was 0,46. The frequencies of the four possible gene combinations in the sample group from Milan were: Ag ^yb =0,53; =0,22; =0,21; Ag ^xb =0,04.The observed frequencies of the factor Ag(a₁) were 0,676 and 0,713, respectively among the Milan and Berne populations.     

Influence of hyperbaric oxygen tension on the metabolism of Candida tropicalis and Rhodococcus erythropolis

Summary The effect on metabolism of hyperbaric dissolved oxygen tension in batch cultures of Candida tropicalis (Cast.) Berkhout and Rhodococcus erythropolis with three different carbon sources was studied in a 20-l bioreactor under controlled conditions. The respiratory quotient was not significantly influenced by dissolved oxygen concentrations up to 40 mg/l oxygen. Elementary cell composition and proportional contents of DNA, RNA, and protein were not markedly influenced by the various oxygen concentrations but depended mainly on the growth rate. It was found that the production of trehalose lipid by R. erythropolis was dependent on the growth rate which could be enhanced by raising the oxygen concentration. The specific activity of catalase was affected more by the nature of the carbon source than by increased oxygen concentration. On the basis of the experimental data the application of oxygen-enriched air for biotechnological processes is discussed.Symbols and abbreviations k_La Specific volumetric oxygen transfer rate - Oxygen consumption rate, grams oxygen per hour and per liter - Carbon dioxide production rate, grams carbon dioxide per hour and per liter - RQ Respiratory quotient, - t Cultivation time - Y_X/S Yield coefficient, grams cell dry weight/grams substrate - Yield coefficient, grams cell dry weight/grams oxygen consumed - Y_kJ Yield coefficient, grams cell dry weight/heat of combustion of the consumed substrate - Y_ave– Yield coefficient, grams cell dry weight/mol available electrons of the consumed substrate     

Maximal oxygen uptake,sweating and tolerance to exercise in the heat

The purpose of this experiment was to determine if tolerance to exercise in the heat is related to maximal oxygen uptake (max ₀₂) and sweating. Seven men with max ₀₂ between 42 and 66 ml/(min·kg) underwent one 2-hr exposure at 24°C T_q while working on a bicycle ergometer at rel ₀₂ of 28% ( ₀₂ = 1.23 1/min). In the hot exposures the high capacity subjects had maximal sweat rates of 800 to 1,000 g/(hr·m²) while the lower capacity men sweated 300 to 400 g/(hr·m²). These differences in sweating were not related to neuromuscular stimuli, ₀₂ (metabolic rate), T_re, T_re, _s, _s or tolerance time. Tolerance to exercise in the heat was not related to maximal ₀₂ capacity when the subjects worked at the same relative load in spite of large differences in sweating. These results question the importance of the rate of sweating for predicting work performance in hot environments.

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Zusammenfassung Das Ziel dieser Untersuchung war, zu prüfen, ob die Toleranz bei Arbeit in der Hitze in einer Beziehung steht zur maximalen O₂-Aufnahme und Schwitzen. Sieben Männer mit V₀₂ zwischen 42 – 66 ml/(min·kg) wurden belastet während 2 Stunden bei T_a 24°C und 3 × 2 Stunden bei 47°C mit Arbeit auf dem Fahrrad-Ergometer bei im Mittel von 28% V₀₂ = 1.23 1/min. Während der Hitzebelastung zeigten die leistungsfähigen Personen Schweissekretionsraten von 800 – 1000 g/(hr·m²) und die wenig leistungsfähigen 300 – 400 g/(hr·m²). Diese Unterschiede waren ohne Beziehung zu neuromuskulären Stimuli, Stoffwechselrate, T_re, T_re, _s, _s oder der Toleranzzeit. Ausdauer bei Arbeit in der Hitze war ohne Beziehung zur maximalen V₀₂-Kapazität, wenn die Personen bei der gleichen relativen Belastung arbeiteten tro grosser Unterschiede im Schwitzen. Die Ergebnisse stellen den Wert der Schweissekretionsrate zur Voraussage der Arbeitsleistung in der Hitze in Frage.

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Resume Dans cette étude, on a cherché à voir si la tolérance au travail sous contrainte de chaleur était en relation avec la possibilité maximum d'absorption de O₂ ( ₀₂) d'une part, de transpirer d'autre part. 7 hommes présentant des ₀₂ compris entre 42 et 66 ml/(min · kg) ont pédalé sur un ergomètre pendant 2 heures par une T_a de 24°C et 3 × 2 heures par 47°C et cela par une ₀₂ relative de 28% ( ₀₂ = 1,25 1/min). Durant l'effort sous contrainte de chaleur, les plus actifs ont eu des sécrétions de sueur de 800 à 1.000 g h^–1 m^–2 et les moins actifs de 300 à 400 g/h · m². Ces différences étaient sans rapport avec les stimulus neuro-musculaires, le taux de métabolisme, T_re, T_re, T_s et T_s ou la durée de tolérance. L'endurance au travail sous contrainte de chaleur n'a pas été fonction de la capacité maximum de ₀₂, lorsque les personnes travaillaient dans des conditions analogues, même si l'on a noté de grandes différences dans la transpiration. Ces résultats mettent en doute la représentativité du taux de sécrétion de sueur comme indicatif des possibilités de travailler en atmosphère chaude.

     

Energetics of the growth of Methanobacterium thermoautotrophicum and Methanococcus thermolithotrophicus on ammonium chloride and dinitrogen

Methanobacterium thermoautotrophicum was grown in continuous culture in a fermenter gassed with H₂ and CO₂ as sole carbon and energy sources, and in a medium which contained either NH₄Cl or gaseous N₂ as nitrogen source. Growth was possible with N₂. Steady states were obtained at various gas flow rates with NH₄Cl and with and the maintenance coefficient varied with the gas input and with the nitrogen source. Growth of Methanococcus thermolithotrophicus in continuous culture in a fermenter gassed with H₂, CO₂ as nitrogen, carbon and energy sources was also examined.Abbreviations molecular growth yield (g dry weight of cells per mol of CH₄ evolved) - growth rate (h^-1) - D dilution rate (h^-1) - rate (h_-1); relation of Neijssel and Tempest and of Stouthamer and Bettenhaussen - energy     

Reversed bohr and root shifts in hemocyanin of the marine prosobranch,Buccinum undatum: Adaptations to a periodically hypoxic habitat

Summary Oxygen binding properties of the hemocyanin-containing blood ofBuccinum undatum were examined in vitro and in vivo under normoxic ( 150 mmHg) and hypoxic ( 50 mmHg) conditions at 10°C. Blood pH and showed a decrease in vivo under hypoxic conditions. Oxygen uptake at high water , was about 18 ml O₂/kg·h (wet weight) and the critical oxygen tension between 25 and 50 mm Hg. In vitro the O₂ binding to hemocyanin showedn-values independent of pH, while both O₂ affinity and oxygen carrying capacity were strongly pH dependent. Oxygen affinity increased below pH=8.1 and thus showed a pronounced reversed Bohr shift in the physiological pH range (7.5<pH<8.1). The oxygen carrying capacity similarly increased markedly with falling pH in the physiological pH range (reversed Root shift). Astrup titration curves showed a metabolic and respiratory acidosis under hypoxic conditions ( 50 mm Hg). The role of hemocyanin in the transport of oxygen in relation to ambient O₂ availability is discussed.     

Aerobic metabolism of the lizardVaranus exanthematicus: Effects of activity, temperature, and size

Summary Oxygen consumption was measured at rest and during spontaneous activity at body temperatures of 25 and 35°C in 14 fasting Savanna monitor lizards,Varanus exanthematicus ranging in weight from 172 to 7500 g. The allometric relationship between metabolic rate at 25°C and body weight (W) is given by: (ml O₂ STPD·g^–1·hr^–1)=0.88W ^–0.43 (Fig. 2). Although statistical comparisons are equivocal, this intraspecific size dependence exceeds that reported for interspecific comparisons among reptiles and other vertebrate groups (Fig 3). A reproducible diurnal pattern of activity was observed in undisturbed animals with minimum values of between 2400 and 0800 h (Fig. 1). Spontaneous activity and generally reached peak values between 1200 and 2000 hrs. The average ratio of active aerobic metabolic rate (AMR) to minimum (standard) aerobic metabolic rate (SMR) was 8.2. This voluntary AMR/SMR inVaranus exceeds the AMR/SMR for most reptiles stimulated to exhaustion. The high aerobic capacity is consistent with other evidence for efficient exchange and transport of respiratory gases inV. exanthematicus; e.g., low or absent intracardiac shunt flow resulting in high arterial saturation and low ventilation and perfusion requirements.     

Energetics of vocalization by an anuran amphibian (Hyla versicolor)

Summary The metabolic demands of vocalization byHyla versicolor were determined by measuring oxygen consumption and whole body lactate content of calling animals. A stepwise multiple regression analysis identified both calling rate (calls/h) and call duration (s/call) as significant determinants of oxygen consumption during calling. These two variables accounted for 84% of the total variation in oxygen consumption observed in calling frogs. Aerobic metabolism increased linearly with calling rate and call duration, reaching a peak value of 1.7 ml O₂/(g·h) at the highest vocalization effort. For comparison, metabolic rates of the same individuals were also measured during short bouts of vigorous locomotor exercise induced by mechanical stimulation. The mean value of was only 62% of the peak , and 5 of 13 frogs had rates of oxygen consumption during calling that exceeded their . Whole body lactate levels were measured in two samples of calling frogs, one collected early in the evening (2100–2115 h) and the other 1.5 h later (2230–2245 h). The frogs in the second sample had significantly lower lactate levels (0.10 mg/g) than the frogs collected early in the evening (0.22 mg/g). Hence, vocalization does not entail the use of anaerobic metabolism, although lactate levels may be slightly elevated at the onset of an evening of calling. Calling rates of unrestrained frogs in a large chorus were measured at regular intervals during an evening. During the first half hour of calling, rates increased gradually from an initial mean value of 600 calls/h at 2030 h to nearly 1400 calls/h at 2100 h. These data indicate that acoustic advertisement byHyla versicolor is among the most energetically expensive activities regularly undertaken by any anuran, and indeed, is the most demanding yet measured in an ectothermic vertebrate.Abbreviations resting rate of oxygen consumption - maximum rate of oxygen consumption - rate of oxygen consumption during forced exercise - rate of oxygen consumption during calling     

The nucleotide sequence ofBeneckea harveyi 5S rRNA

Summary The complete sequence of the 5S rRNA from the bioluminescent bacterium,Beneckea harveyi has been determined to be p U G C U U G G C G C C A U A G C G A U U-G G A C C C A C U G A (U) C U U C A U U C C-G A A C C A G A A G U G A A C G A A U U A-G G C C G A U G G U G U G U G G G G C U-C C C C A U G U A G A G U A G G A A U C G-C C A G G U (U)_OH.Two sites of sensitivity to ribonuclease T₂ cleavage were identified; at A₄₁ and either A₅₄ or A₅₅. Comparison with existing sequence information fromEscherichia coli andPhotobacterium phosphoreum clarifies the amount of diversity among the bioluminescent bacteria and provides further insight into their phylogenetic position. Sequence heterogeneities were encountered and the importance of these in interpreting 5S rRNA data is discussed.     

Carbon dioxide desorption from fermentation broth by use of oxygen vectors

The ability of oxygen vector to extract produced carbon dioxide has been tested in an anaerobic fermentation. During the continuous culture of Clostridium acetobutylicum at pH 4.6 and at a dilution rate of 0.124 h^–1, a feed composed of an emulsion of 18.5% by volume of Forane F66E was able to extract about 9% of the total CO₂ produced under CO₂ partial pressure equal to 0.42 atm. A theoretical evaluation of the extracted amount, based on the hypothesis of total saturation of the vector by carbon dioxide, has lead to very good agreement.List of Symbols [AA] g/l acetic acid concentration - [BA] g/l butyric acid concentration - D 1/h Q _w /V dilution rate - [ETH] g/l ethanol concentration - H _w Henry constant of CO₂ for water at 37°C (=23.91 mmol/(l atm)) - H _F Henry constant of CO₂ for Forane at 37°C (=83.4 mmol/(l atm)) - H _i g/mol molar mass of componenti - P _i atm partial pressure of gasi - W _w l/h aqueous flow - Q_f 1/h Forane flow - mmol/(lh) dissolved CO₂ flow in aqueous effluent - mmol/(lh) CO₂ gas flow - mmol/(lh) CO₂ gas flow without Forane - mmol/(lh) CO₂ gas flow with Forane - mmol/(lh) total CO₂ production - r _X g/(lh) biomass production rate - r _G mmol/(lh) total gas flow - mmol/(lh) hydrogen production - mmol/(lh) nitrogen flow - r _S mmol/(lh) glucose input - V 1 fermentor volume     

Physiological mechanisms for underwater endurance: Canada goose (Branta canadensis) versus Pekin duck (Anas platyrhynchos)

Maximum submergence time of Canada geese was 18% of that of similarly sized Pekin ducks. Due to a smaller respiratory system volume the oxygen store of Canada geese was 82% of that of Pekin ducks, accounting for approximately 33% of the difference in underwater survival times. The respiratory properties and volume of the blood were similar in both species. Both species utilised approximately 79% of the respiratory oxygen store and 90% of the blood oxygen store. Therefore, most of the species difference in survival times was due to a less effective oxygen-conserving cardiovascular response (bradycardia, peripheral vasoconstriction) in Canada geese. Duck cardiac chronotropic sensitivity to hypoxia during submergence was twice that observed in geese. Furthermore, a lower hypoxic ventilatory response was observed in geese than in ducks. Density of monoamine varicosities in hindlimb artery walls was lower in geese than ducks. However, electrical stimulation of the hindlimb muscles did not cause ascending vasodilation during submergence in either species, perhaps due to higher levels of catecholamines in submerged geese. We conclude that the major difference between species is higher oxygen chemosensitivity in ducks which effects a much more rapid and efficacious oxygen-conserving response during forced submergence.Abbreviations ATPS · BTPS · STPD CNS central nervous system - EEG electroencephalogram - ECG electrocardiogram - EDTA ethylenediaminetetra-acetic acid - HPLC high performance liquid chromatography - fractional oxygen concentration of inspired air - pre-immersion fractional concentration of oxygen in the respiratory system - pre-emersion fractional concentration of oxygen in the respiratory system - [Hb] haemoglobin concentration - Hct haematocrit - HR heart rate - M _B body mass - M _b brain mass - M _h heart mass - partial pressure of carbon dioxide in arterial blood - partial pressure of oxygen in arterial blood - SPG sucrose-potassium phosphate-glyoxylic acid - t _d maximum underwater survival time - respiratory minute volume - V _pl plasma volume - V _rs respiratory system volume - accessible respiratory system oxygen store - total non-myoglobin-bound oxygen store - V _tb blood volume - blood oxygen store     

Sulfur isotope values in a forested catchment over four years: Evidence for oxidation and reduction processes

A small catchment on the Swedish West Coast has been studied over four years to determine S dynamics by using S isotope ratios. A Norway spruce dominated forest covers the catchment, and small peat areas occur in the lower parts of the catchment. The runoff values varied both during the year, and from year to year. Over the period from February 1990 to December 1993, the values ranged from — 1%. to +11%. Over the same period, the throughfall values ranged from +1%. to +15%. There was no correlation (r ²= 0.01; Pr(F)=0.57) between values in throughfall and runoff. Since the only input of S to the catchment is atmospheric deposition, the long-term runoff S mass flux is controlled by the deposition. Therefore, processes in the catchment are responsible for the variation in the runoff values. During periods with enriched runoff, bacterial dissimilatory SO ₄ ^2– reduction occurs in the catchment. After very dry periods, oxidation of this reduced S, which is³²S-enriched, can be traced in runoff. Previous studies of the catchment have not been able to distinguish between: 1) oxidation of reduced S and dry deposition, and 2) reduction and adsorption. From the current study, it can be concluded that adsorption and dry deposition cannot cause the observed variation in runoff .     

Growth and product formation of actinomycetes cultivated at increased total pressure and oxygen partial pressure

Summary Influence of pressure (P) and oxygen partial pressure ( ) on cultivation of various Streptomyces spp. and Micromonospora purpurea was examined in pressurized air-lift and stirred tank fermenters. The maximum was 2100 mbar. Growth and product formation of all cultures tested were markedly influenced by higher than 1000 mbar. There is evidence that wild strains are more oxygen tolerant than production strains. At a certain the metabolic activities of all cultures were inhibited. However, results obtained with S. aureofaciens and S. rimosus indicated an increase in specific product formation rate at elevated pressure. With increase in oxygen tension incorporation of oxygen into tetracycline molecules was enhanced. Since elevated oxygen tension can either show inhibiting effects or may be used for regulation of product formation and selectivity, the influence of should be determined in an appropriate experimental set-up for each process.Offprint requests to: U. Onken     

Oxygen controlled batch cultivations of Schizophyllum commune for enhanced production of branched β-1,3-glucans

Oxygen and shear stress are the key factors for enhanced glucan production with Schizophyllum commune. During batch cultivation control of or (specific oxygen uptake rate) was achieved by variation of the impeller speed. Biomass was modelled by using the carbon and oxygen balance derived from exhaust data. At mycel growth a of 0.042 h^–1 presents just the border before oxygen limitation arises and is simultaneously the optimum operation condition for maximum glucan formation. Related to an overall cultivation time of 72 h a maximum of both productivity (4.3 kg m^–3 d^–1) and yield (13 kg m^–3) were obtained.List of Symbols C kg m^–3 concentration - k _L a h ^–1 volume related oxygen transfer coefficient - K _s mol m^–3 substrate saturation constant - N rpm impeller speed - % oxygen partial pressure of the liquid phase - kg m^–3h^–1 oxygen uptake rate - h^–1 specific oxygen uptake rate, kg O₂ (kg biomass h)^–1 - t h time - yield coefficient (biomass formed/oxygen consumed) Greek Symbols h^–1 specific growth rate Indices O ₂ oxygen - X biomass - L liquid phase - * gas/liquid interface - S substrate (glucose) Dedicated to the 65th birthday of Professor Fritz Wagner.This work was kindly supported in parts by B. Braun Biotech International. The authors are grateful to Prof. Dr. Fritz Wagner for scientific support and appreciate the technical assistance of Detlev Rasch     

Interaction between catabolism and anabolism in the oxidative assimilation of dissolved organic carbon

Catabolism is tightly coupled to anabolism in substrate-limited cultures. However, the dissolved organic carbon (DOC) distribution between catabolism and anabolism has been hardly studied. Based on a balanced DOC reaction, the DOC distribution between catabolism and anabolism was defined using a ratio of the DOC channeled into CO₂ ( ) to that DOC converted to biomass (S _g). A /S _g-dependent growth yield model was proposed for substrate-limited cultures and was verified using the literature data obtained in the oxidative assimilation processes of different types of organic substrates. The model showed that the growth yield (Y _s) was proportional to anabolic activity, but was inversely related to catabolic activity. Results indicated that both Y _s and /S _g varied markedly with the free energy of oxidation of the organic substrate. Further, the observed phenomena were closely associated with maintenance metabolism under substrate-limited conditions.     

Thermoregulation,gas exchange,and ventilation in Adelie penguins (Pygoscelis adeliae)

Summary Adelie penguins (Pygoscelis adeliae) experience a wide range of ambient temperatures (T _a) in their natural habitat. We examined body temperature (T _b), oxygen consumption ( ), carbon dioxide production ( ), evaporative water loss ( ), and ventilation atT _a from –20 to 30 °C. Body temperature did not change significantly between –20 and 20°C (meanT _b=39.3°C).T _b increased slightly to 40.1 °C atT _a=30°C. Both and were constant and minimal atT _a between –10 and 20°C, with only minor increases at –20 and 30°C. The minimal of adult penguins (mean mass 4.007 kg) was 0.0112 ml/[g·min], equivalent to a metabolic heat production (MHP) of 14.9 Watt. The respiratory exchange ratio was approximately 0.7 at allT _a. Values of were low at lowT _a, but increased to 0.21 g/min at 30°C, equivalent to 0.3% of body mass/h. Dry conductance increased 3.5-fold between –20 and 30°C. Evaporative heat loss (EHL) comprised about 5% of MHP at lowT _a, rising to 47% of MHP atT _a=30°C. The means of ventilation parameters (tidal volume [VT], respiration frequency [f], minute volume [I], and oxygen extraction [ ]) were fairly stable between –20 and 10°C (VT did not change significantly over the entireT _a range). However, there was considerable inter- and intra-individual variation in ventilation patterns. AtT _a=20–30°C,f increased 7-fold over the minimal value of 7.6 breaths/min, and I showed a similar change. fell from 28–35% at lowT _a to 6% atT _a=30°C.Abbreviations C thermal conductance - EHL evaporative heat loss - oxygen extraction - f respiratory frequency - MHP metabolic heat production - evaporative water loss - LCT lower critical temperature - RE respiratory exchange ratio - T _a ambient temperature - T _b body temperature - rate of oxygen consumption - rate of carbon dioxide production - I inspiratory minute volume - VT tidal volume