Effects of temperature on microbial ethanol production. III. The influence of the temperature on the relation existing between the specific ethanol formation rate of the yeast Saccharomyces cerevisiae Sc 5 and the ethanol concentration in the culture medium

The ethanol-inhibitory behaviour of the yeast Saccharomyces cerevisiae Sc 5 was found to be characterized by a continual-linear relation between the specific ethanol formation rate and the ethanol concentration. Therefore the simple equation could be applied for it. It is shown that this model is correct only then, if all of the process parameters are in their optimum. Out of the optimum temperature range the characteristics of the function ν = f(P) change in such a way that in regard to the ethanol concentration P twc linear relations exist for each suboptimum temperature: and a non-linear equation is current for each superoptimum temperature: where b_T is also a function of the temperature and always less than 1. Taking as a basis these equations the specific ethanol formation rate of the used strain can be calculated for the whole biokinetic P/T-sphere of ethanol production.     

Survival of white-tailed deer fawns in the grasslands of the northern Great Plains

Environmental factors, such as forest characteristics, have been linked to fawn survival in eastern and southern white-tailed deer (Odocoileus virginianus) populations. In the Great Plains, less is known about how intrinsic and habitat factors influence fawn survival. During 2007–2009, we captured and radiocollared 81 fawns in north-central South Dakota and recorded 23 mortalities, of which 18 died before 1 September. Predation accounted for 52.2% of mortality; remaining mortality included human (hunting, vehicle, and farm accident; 26.1%) and hypothermia (21.7%). Coyotes (Canis latrans) accounted for 83.3% of predation on fawns. We used known-fate analysis in Program MARK to estimate summer (15 May–31 Aug) survival rates and investigated the influence of intrinsic and habitat variables on survival. We developed 2 a priori model sets, including intrinsic variables and a test of annual variation in survival (model set 1) and habitat variables (model set 2). Model set 1 indicated that summer survival varied among years (2007–2009); annual survival rates were 0.94 (SE = 0.06, n = 22), 0.78 (SE = 0.09, n = 27), and 0.54 (SE = 0.10, n = 32), respectively. Model set 2 indicated that survival was further influenced by patch density of cover habitats (Conservation Reserve Program [CRP]-grasslands, forested cover, and wetlands). Mean CRP-grassland and wetland patch density (no. patches/100 ha) were greater (P < 0.001) in home-range areas of surviving fawns ( = 1.81, SE = 0.10, n = 63; = 1.75, SE = 0.14, n = 63, respectively) than in home-range areas of fawns that died ( = 0.16, SE = 0.04, n = 18; = 1.28, SE = 0.10, n = 18, respectively). Mean forested cover patch density was less (P < 0.001) in home-range areas of surviving fawns ( = 0.77, SE = 0.10, n = 63) than in home-range areas of fawns that died ( = 1.49, SE = 0.21, n = 18). Our results indicate that management activities should focus on CRP-grassland and wetland habitats in order to maintain or improve fawn survival in the northern Great Plains, rather than forested cover composed primarily of tree plantings and shelterbelts. © 2012 The Wildlife Society.     

Buoyant densities of natural and synthetic DNA's in CsCl and Cs2SO4 considered as sequence-dependent properties

The buoyant densities of natural and synthetic DNA's can be accurately interrelated if second-neighbor influences are taken into account. We derive the following expressions, based partly on the buoyant densities of six synthetic DNA's, for the buoyant densities ρ (g/cm³) of DNA's having random sequences. In CsCl, and in Cs₂SO₄, . In these equations, H_G is the mole fraction of G : C base pairs in the DNA and the buoyant densities are calculated relative to densities for E. coli DNA of 1.703 and 1.426 (g/cm³) in CsCl and Cs₂SO₄, respectively.     

Construction of Prediction Intervals in Location-Scale Families

Let x₁ ≤x₂ ≤x₃ … ≤x_r be the r smallest observations out of n observations from a location-scale family with density $ \frac{1}{\sigma}f\left({\frac{{x - \mu}}{\sigma}} \right) $ where μ and σ are the location and the scale parameters respectively. The goal is to construct a prediction interval of the form $ \left({\hat \mu + k_1 \hat \sigma,\,\hat \mu + k_2 \hat \sigma} \right) $ for a location-scale invariant function, T(Y) = T(Y₁, …, Y_m), of m future observations from the same distribution. Given any invariant estimators $ \hat \mu $ and $ \hat \sigma $, we have developed a general procedure for how to compute the values of k₁ and k₂. The two attractive features of the procedure are that it does not require any distributional knowledge of the joint distribution of the estimators beyond their first two raw moments and $ \hat \mu $ and $ \hat \sigma $ can be any invariant estimators of μ and σ. Examples with real data have been given and extensive simulation study showing the performance of the procedure is also offered.     

Growth characteristics of a thermotolerant strain of lodderomyces elongisporus grown on sucrose

A thermotolerant yeast species of Lodderomyces elongisporus EH 60 was isolated and physiologically characterized. This yeast possesses a high specific growth rate with μ_max = 0.61 h^?1. The dependence of the specific growth rate and cell yield on temperature, dilution rate, sucrose concentration and pH-value is investigated. Sucrose concentrations greater than 10 g/l inhibit the growth velocity. The specific growth rate μ can be calculated by a simple combination equation in the form: . The total optimum values for a sucrose-based continuous growth process with regard to the optimum cell yeild are: Y_S = 0.50 g DM/g S. T_opt. = 38,6 °C and D_opt. = 0,35 h^?1. The function Y_S = f(D, T) is represented by a total model.     

Conformational aspects of polypeptides. XVII. Synthesis of oligomers and co-oligomers derived from L-alanine and L-glutamic acid

A series of oligomers was synthesized of the form: Where Z is the benzyloxycarbonyl group and n = 2, 3, 5, 10. We encountered difficulty in dissolving the decamer in any solvent except strong organic acids. We therefore prepared co-oligomers of the type: where (a) w = x = y = 1; (b) w = 0, x = y = 3; and (c) w = x = y = 3. A series of model compounds composed of glycine L -alamine and γ-methyl-L -glutamate were also prepared. We converted manyof the benzyloxycarbonyl oligopeptides into their corresponding acetyl derivatives. Some of these peptides were synthesized by mixed anhydride and active ester techniques while others were prepared via azide coupling techniques using the tert-butoxycarbonylhydrazide blocking group. All reactions proceeded with retention of configuration.     

Oxygen mass transfer and gas holdup in a bubble column bioreactor with biosynthesis liquids

The influence of the rheology of some antibiotic biosynthesis liquids produced by Streptomyces aureofaciens, Nocardia mediterranei and Penicillium chrysogenum on the volumetric liquid phase oxygen transfer coefficient, k_La, and gas holdup, ε_G, together with the influence of superficial gas velocity, were studied in a bubble column bioreactor, using samples of fermentation liquids taken from industrial stirred tank fermenters, at 30-hour intervals during fermentation batch. The results were compared to those of previous studies from literature on non-Newtonian homogeneous fluids, such as CMC-Na, xanthan and starch solutions, respectively. In the heterogeneous broths, ε_G and k_La decreased with increasing apparent viscosity of the broth and increased with increasing superficial velocity. The experimental data were correlated using non-linear regression with correlation coefficients above 0.85.     

Age and growth of pearly razorfish,Xyrichtys novacula (Linnaeus 1758), in the central Mediterranean Sea

Age and growth of pearly razorfish Xyrichtys novacula (Labridae) were determined in specimens caught on sandy bottoms by surrounding nets and lines (depth range 5–30 m) between January 2000 and December 2002. The study location was in the central Mediterranean Sea. For this purpose the annual growth increments (annuli) in sagittae were analysed. A total of 470 individuals of X. novacula, ranging from 49 to 200 mm TL (total length), were examined. Conversion between total length and standard length was calculated and represented by the relationship: . Edge analysis on otoliths was carried out to validate seasonality deposition. Seven age‐classes were determined from 0+ to 6+. The linear relationship between maximum otolith length (OL) and TL was summarized in the equation . The estimated parameters of the von Bertalanffy growth function were L = 175.05 mm, k = 0.80 year^?1, t₀ =?0.73 years and the growth performance index calculated as (Φ = 2.39). The length–weight relationship W = 0.0139 TL^2.9326 described an isometric growth for the species in this area.     

The isomerization of D-glucose into D-fructose catalyzed by whole-cell immobilized glucose isomerase. The dependence of the intrinsic rate of reaction on substrate concentration,pH, and temperature

The relation between the intrinsic rate of the glucose-fructose isomerization catalyzed by whole-cell immobilized glucose isomerase and the substrate concentration can be described with the kinetic model The numerical values of k₁, k_?1, k₂, and k_?2 have been determined from low-conversion experiments starting from pure glucose or fructose solutions, and are presented as a function of pH and temperature. The difference between the overall chemical reaction rate determined in high-conversion experiments and that calculated from the individual k₁, k_?1, k₂, and k_?2 values is less than 10%.     

Inhibition-threshold substrate concentrations

A proposed substrate inhibition model (M. C. Tseng and M. Wayman, Can. J. Microbiol., 21 , 994 (1975)), ((1)) ((2)) derived from yeast growth rates has been applied to data for bacterial growth: Pseudomonas methanica grown on methanol and Arthrobacter AK19 grown on n-butanol. The model represents the experimental data very well.     

The parabolic pattern of animal growth: determination of equation parameters and their temperature dependencies

1. Parabolic (power) growth is characteristic of many aquatic poikilothermic animals for certain stages of their development. The parabolic pattern describing growth in weight (or length) under constant ambient conditions can be expressed in the following general form: where Y is growth rate (or specific growth rate), X is animal size, and Ω and τ are coefficients. The constancy of ambient conditions is of cardinal importance in determining τ. The problem of maintaining a constant level of nutrition can be reliably solved only by the presence of food in excess of demand. Data satisfying these requirements have demonstrated that τ does not depend on factors such as temperature, and can be assumed to be independent of ambient conditions. In the growth rate-weight equation, τ ranges between 0.5 and 0.85 for animals representing a variety of taxonomic groups. 2. The coefficient Ω. is affected by ambient conditions (e. g. temperature, amount of food). Its value reflects the ‘level’ of the growth rate-size relationship under given conditions. For a specific time period, Ω can be computed from the following formula: where X₁ and X₂ are the animal sizes (weights, lengths) at time t₁ and t₂, the beginning and end of the time period. The calculated value of Ω corresponds to the average intensity of the ambient factor (F) affecting the growth during the period between the two observations. If the values of the Ω are calculated for wide range of the factor, the relationship between the Ω. and F, Ω=f(F), can be determined. The function can be then incorporated into the parabolic equation of growth, as 3. Dependence of the development rate (1/D, where D is time interval needed to complete a given stage) on temperature (T), and dependence of Ω on T, are both described by sigmoid-shape curves. The broad intermediate part of these curves, a range to which animals are adapted in nature, can be approximated by straight line functions. For two groups, pan-size sockeye salmon (Oncorhynchus nerka) and different species of chironomid larvae, it was shown that an equation combining parabolic growth and linear temperature patterns describes accurately the variability observed in growth rates under experimental and natural conditions.     

A preliminary survey of Tilapia nurseries on Lake Kariba during 1967/68

Summary Young Tilapia on Lake Kariba show a marked preference for shallow water but this is complicated by fluctuating lake levels, the floating weed Salvinia auriculata and the Tigerfish Hydrocynus vittatus. Tilapia nurseries found to date occur on shallow sloping shores predominently in the bush cleared areas and overlie Lower Karroo and Marly Sandstones. They are characterised by having a minimum of Salvinia coverage and a diversity of emergent and submerged aquatic plant growth arranged in fairly definate zones.Rising lake levels provide the most favourable conditions for young Tilapia in the shallow, temporary nurseries. Receding water levels force the fish into Cerotophyllum and Potamogeton beds of the deeper water. Tilapia do not leave cover until a length of between 17 cm and 19 cm is attained. Above this size they are considered reasonably safe from Hydrocynus. The impact on Tilapia of three nocturnal predators is considered insignificant at the present time. Salvinia has the effect of causing lower oxygen tensions and retardation of essential submerged aquatic vegetation and is considered detrimental to the Tilapia fishery. Submerged aquatic plants are highly desirable to protect young Tilapia from predation during receding water levels.Presented at the Symposium on Standing Waters, Grahamstown, South Africa, in July 1968.     

A posteriori Investigation of Spatial Arrangements in Gnathostomulida and Copepoda

Copepods at MHTL and gnathostomulids from MHTL to sublittoral sands were studied in 162 samples from Tucker's Town Cove beach, Bermuda. Species were analyzed for mean density (X̄), mean crowding ( ), and patchiness ( /X) using Lloyd's a posteriori statistic for mean crowding. Diversity was computed using the Shannon-Wiener Index (H′). Copepoda were found to be nearly three times more abundant than Gnathostomulida at the MHSL site. 74% of the copepods were found in the surface cm of sediment while 87% of the gnathostomulids were located between 1–4 cm deep and within the RPD layer. Similar gnathostomulid distributions were found at MSL and sublittorally. Mean density and mean crowding were highly variable for the numerically dominant species in each group, whereas patchiness was relatively constant with values ranging between /X̄ = 1.50 to 2.73 for P = 0.05. Such consistency in patchiness between two diverse taxa having distinctly different vertical distributions may suggest that there exists an optimum degree of patchiness for interstitial fauna and that the optimum values may lie within a range similar to that of the numerically dominant Copepoda and Gnathostomulida. Overall patchiness was slightly higher in the gnathostomulids and in the rarer species as predicted by Lloyd's statistic. Diversity was higher in the Copepoda, attributable primarily to species richness.     

Confidence Intervals on Ratios of Variance Components for the Unbalanced Two Factor Nested Model

The model considered in this article is the two-factor nested unbalanced variance component model: for p = 1, 2, …, P; q = 1, 2, …, Q_p; and r = 1, 2, …, R_pq. The random variables Y_pqr are observable. The constant μ is an unknown parameter, and A_p, B_pq and C_pqr are (unobservable) normal and independently distributed random variables with zero means and finite variances σ²_A, σ²_B, and σ²_C, respectively. Approximate confidence intervals on ?_A and ?_B using unweighted means are derived, where The performance of these approximate confidence intervals are evaluated using computer simulation. The simulated results indicate that these proposed confidence intervals perform satisfactorily and can be used in applied problems.     

A Stochastic Model for Surname Evolution

Surnames are inherited in much the same way as biological traits like alleles of one locus. Assuming the heritability of surnames, a simple stochastic model for X, the total number of occurrences of a surname, the Consul distribution defined by the probability mass function: for x = 1, 2, 3,… and zero otherwise and where either (i) m is a positive integer when 0 ≤ θ ≤ 1 such that θ ≦ mθ ≦ 1, or (ii) m≤0, θ ≤0 such that mθ 1, can be arrived at by considering the branching process mechanism. Some applications of the model to real data are also considered.     

Bayesian Bootstrap Clones for Censored Markov Chains

In this article, we consider r observations from a non‐homogeneous censored Markov chain, with transition probability matrix P. For the product estimator of P proposed by Aalen and Johansen (1978) and Phelan (1988), we investigate the behavior of Bayesian bootstrap clones to approximate the sampling distribution of , and then construct approximate confidence interval. It is shown that the approximation based on the random‐weighted distribution is first‐order consistent. The performance of the Bayesian bootstrap clones (BBC) is also discussed by small sample simulation. Finally, we illustrate the BBC procedure in the application to the WHO malaria survey data (cf. Singer and Cohen 1970).     

Effects of temperature on microbial ethanol production. II. A thermodynamic interpretation of the temperature profile curve of ethanol production

An attempt is made to give a thermodynamic interpretation of the complete temperature profile curve of ethanol formation. Taking into consideration an enhancing competition between thermal activation and thermal deactivation of ethanol formation at increasing temperatures and supposing that the ethanol production is affected by a reversible and an irreversible term of thermal deactivation of a modified ARRHENIUS equation being current for the total biokinetic sphere may be derived: . The quantities ΔH and ΔH^D_2T are identical with the temperature functions of the change of entropy caused by reversible and irreversible deactivation of ethanol formation, respectively. Accordingly for the yeast strain Saccharomyces cerevisiae Sc 5 the calculated entropy coefficients of reversible and irreversible thermal deactivation of ethanol formation amount to C = (0.245± 0.013) kJ/mol · deg.² and C = (1.657 ± 0.046) kJ/mol · deg.².     

Polarized fluorescence in an electric field. A model calculation with application to the geometry of the 2-hydroxy-4,4′-diamidinostilbene–DNA complex

Theoretical expressions are derived for the change in the polarized components of the fluorescence, resulting from the orientation of a rigid molecule bearing a chromophore with arbitrary angles for the absorption and transition moments \documentclass{article}\pagestyle{empty}\begin{document}$ \vec \mu _a $\end{document} and \documentclass{article}\pagestyle{empty}\begin{document}$ \vec \mu _e $\end{document} with respect to the molecular axis. The break in the symmetry relation H_V = V_H is related to the tilt angle between \documentclass{article}\pagestyle{empty}\begin{document}$ \vec \mu _a $\end{document} and \documentclass{article}\pagestyle{empty}\begin{document}$ \vec \mu _e $\end{document}. The theory is applied to a sonicated DNA–2-hydroxy-4,4′-diamidinostilbene complex, in the blue and red emission bands of this peculiar dye. Simultaneous measurements of linear dichroism and fluorescence lead to the determination of an angle of 47° between a fluorescent bound dye and the DNA axis, with no difference for the blue- and red-emitting species, but confirm the presence of nonfluorescent bound dye in a more perpendicular arrangement.     

Einfluß extracellulärer Kaliuminoenkonzentrationen auf die celluläre Natriumionenkonzentration von Lodderomyces elongisporus D

It was found that the cellular Na⁺-concentration (C) of Lodderomyces elongisporus D is depended on the extracellular K⁺-concentration (C). The relationship can be described by an equation in the form The function of the natrium ion seem to be to support the utilisation rate of potassium ion at lower extracellular K⁺-concentration.     

Determination of thermodynamic functions from scanning calorimetry data. II. For the system that includes self-dissociation / association process

The basic relations between the molar fractions and the scanning calorimetry data for the system that includes self-dissociation/association process such as are presented, where m_i is the stoichiometric coefficient of the ith state A_i. The relations are described for each state j as where f_j(T) is the molar fraction function of state j and ΔH_j(T) is the difference enthalpy function of the system referred to the state j, which can be obtained by scanning calorimetry; R is the gas constant; and T is the absolute temperature. By these relations, scanning calorimetry data can be deconvoluted in order to determine the thermodynamic functions by means of single and double deconvolution. The concentration dependence of the data is analyzed by a method presented in this paper. The nonlinear least squares fitting method for the determination of the functions is discussed. For an example of the application of this method to the actual scanning calorimetry data, thermodynamic data of multistate thermal transition of Vibrio parahaemolyticus hemolysin are analyzed.