Approximation by complex Phillips–Stancu operators in compact disks under exponential growth conditions

2014 ◽  
Vol 234 ◽  
pp. 309-315 ◽  
Author(s):  
Sorin G. Gal ◽  
Vijay Gupta
Filomat ◽  
2015 ◽  
Vol 29 (5) ◽  
pp. 1007-1019 ◽  
Author(s):  
Nursel Çetin

In this paper, we establish some theorems on approximation and Voronovskaja type results for complex modified Sz?sz-Mirakjan-Stancu operators attached to analytic functions having exponential growth on compact disks. Also, we estimate the rate of convergence and the exact order of approximation.


2012 ◽  
Vol 61 (2) ◽  
pp. 153-165 ◽  
Author(s):  
Sorin G. Gal ◽  
Vijay Gupta ◽  
D. K. Verma ◽  
P. N. Agrawal

2020 ◽  
Vol 17 (166) ◽  
pp. 20190827 ◽  
Author(s):  
Ethan Levien ◽  
Jane Kondev ◽  
Ariel Amir

In isogenic microbial populations, phenotypic variability is generated by a combination of stochastic mechanisms, such as gene expression, and deterministic factors, such as asymmetric segregation of cell volume. Here we address the question: how does phenotypic variability of a microbial population affect its fitness? While this question has previously been studied for exponentially growing populations, the situation when the population size is kept fixed has received much less attention, despite its relevance to many natural scenarios. We show that the outcome of competition between multiple microbial species can be determined from the distribution of phenotypes in the culture using a generalization of the well-known Euler–Lotka equation, which relates the steady-state distribution of phenotypes to the population growth rate. We derive a generalization of the Euler–Lotka equation for finite cultures, which relates the distribution of phenotypes among cells in the culture to the exponential growth rate. Our analysis reveals that in order to predict fitness from phenotypes, it is important to understand how distributions of phenotypes obtained from different subsets of the genealogical history of a population are related. To this end, we derive a mapping between the various ways of sampling phenotypes in a finite population and show how to obtain the equivalent distributions from an exponentially growing culture. Finally, we use this mapping to show that species with higher growth rates in exponential growth conditions will have a competitive advantage in the finite culture.


2020 ◽  
Vol 29 (1) ◽  
pp. 37-44
Author(s):  
AYDIN IZGI ◽  
SEVILAY KIRCI SERENBAY

This paper presents a study on the approximation properties of the operators constructed by the composition of Chlodowsky operators and Szasz-Durrmeyer operators. We give the approximation properties and obtain a Voronovskaya-type result for these operators for analytic functions of exponential growth on compact disks. Furthermore, a numerical example with an illustrative graphic is given to compare for the error estimates of the operators.


1991 ◽  
Vol 48 (7) ◽  
pp. 1136-1144 ◽  
Author(s):  
S. S. Bates ◽  
A. S. W. de Freitas ◽  
J. E. Milley ◽  
R. Pocklington ◽  
M. A. Quilliam ◽  
...  

Nitzschia pungens f. multiseries (clone NPARL) was grown in nonaxenic batch culture under a range of growth conditions. Domoic acid (DA) was not detected during exponential growth, but production promptly started at a rate of approximately 1 pg DA∙cell−1∙d−1 at the onset of the stationary phase, in this case induced by silicate limitation. Cellular DA reached a maximum of 7 pg∙cell−1; thereafter, DA production continued at the same rate, with cellular levels remaining relatively constant due to concurrent release of DA into the culture medium. DA production ceased in the absence of nitrogen during the stationary phase, but resumed when nitrate was added back to the medium. Low irradiance slowed the division rate and consequently delayed the attainment of the stationary phase, but DA production rates were comparable with the control once stationary phase was reached. Cells during the dark period of a light–dark cycle, or placed into darkness, or in the presence of the photosynthetic inhibitor DCMU promptly ceased DA production. We conclude that at least three conditions are required for DA production by clone NPARL: cessation of cell division, availability of nitrogen during the stationary phase, and the presence of light. Growth in medium f/2 fulfils these requirements.


2019 ◽  
Vol 116 (6) ◽  
pp. 1952-1957 ◽  
Author(s):  
Rebecca Zhuo ◽  
Feng Zhou ◽  
Xiaojin He ◽  
Ruojie Sha ◽  
Nadrian C. Seeman ◽  
...  

Self-replication and exponential growth are ubiquitous in nature but until recently there were few examples of artificial self-replication. Often replication is a templated process where a parent produces a single offspring, doubling the population in each generation. Many species however produce more than one offspring at a time, enabling faster population growth and higher probability of species perpetuation. We have made a system of cross-shaped origami tiles that yields a number of offspring, four to eight or more, depending on the concentration of monomer units to be assembled. The parent dimer template serves as a seed to crystallize a one-dimensional crystal, a ladder. The ladder rungs are then UV–cross-linked and the offspring are then released by heating, to yield a litter of autonomous daughters. In the complement study, we also optimize the growth conditions to speed up the process and yield a 103increase in the growth rate for the single-offspring replication system. Self-replication and exponential growth of autonomous motifs is useful for fundamental studies of selection and evolution as well as for materials design, fabrication, and directed evolution. Methods that increase the growth rate, the primary evolutionary drive, not only speed up experiments but provide additional mechanisms for evolving materials toward desired functionalities.


2010 ◽  
Vol 76 (9) ◽  
pp. 2908-2915 ◽  
Author(s):  
Marina Muñoz-Cuevas ◽  
Pablo S. Fernández ◽  
Susan George ◽  
Carmen Pin

ABSTRACT The dynamic model for the growth of a bacterial population described by Baranyi and Roberts (J. Baranyi and T. A. Roberts, Int. J. Food Microbiol. 23:277-294, 1994) was applied to model the lag period and exponential growth of L isteria monocytogenes under conditions of fluctuating temperature and water activity (aw) values. To model the duration of the lag phase, the dependence of the parameter h 0, which quantifies the amount of work done during the lag period, on the previous and current environmental conditions was determined experimentally. This parameter depended not only on the magnitude of the change between the previous and current environmental conditions but also on the current growth conditions. In an exponentially growing population, any change in the environment requiring a certain amount of work to adapt to the new conditions initiated a lag period that lasted until that work was finished. Observations for several scenarios in which exponential growth was halted by a sudden change in the temperature and/or aw were in good agreement with predictions. When a population already in a lag period was subjected to environmental fluctuations, the system was reset with a new lag phase. The work to be done during the new lag phase was estimated to be the workload due to the environmental change plus the unfinished workload from the uncompleted previous lag phase.


1981 ◽  
Vol 27 (8) ◽  
pp. 835-840 ◽  
Author(s):  
James T. McGarrity ◽  
John B. Armstrong

During exponential growth, strain AW405 of Escherichia coli K-12 did not regulate the fatty acid composition of its lipids in response either to temperature or to the addition of NaCl, KCl, or MgCl2 to the medium. Growth was severely restricted at temperatures below 21 °C. Differential scanning calorimetry (DSC) of the isolated lipids from a culture with a typical exponential-phase composition yielded a broad transition, extending from approximately 0 to 33 °C, with a midpoint at 19 °C.During late stages of growth, the fatty acid composition changed. The percentage of palmitic acid increased and cyclopropane fatty acids replaced some of the equivalent unsaturated fatty acids. The increase in palmitate seemed largely independent of growth conditions, whereas the increase in the cyclopropane fatty acids was stimulated by the addition of salts or sucrose. Cultures grown in the presence of sucrose also had higher cyclopropane fatty acid levels during exponential growth. DSC of lipids from a sucrose culture, in which the compositional changes were most pronounced, yielded a much narrower transition with a midpoint at 27 °C.


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