ISSN: 2644-1381
Elettreby MF and Ahmed E*
Received: April 22, 2020; Published: May 01, 2020
*Corresponding author: E Ahmed, Mathematics department, Faculty of Science, Mansoura 35516, Egypt
DOI: 10.32474/CTBB.2020.02.000143
Extremal optimization is applied in honeybee foraging and solving medical goods supply needed in Covid-19 management.
Extremal optimization (EO) [1] is a metaheuristic method [2] which is quite similar to the way the immune system (IS) renews its cells. This dynamic is called extremal dynamics [3]. It can explain the long-range memory of the immune system even without the persistence of antigens. The reason is that if a system evolves according to such dynamics then the annihilation probability for a clone (a type of cells) that has already survived for time t is proportional to 1/(1+ tc) , where c is a positive constant. Therefore, the longer it lives the higher the probability that it will continue to survive. This is the memory effect observed in the immune system. Consider a system of N elements, each element assigned a single scalar variable x(i), i = 1,2, . . ., N drawn from the fixed probability distribution function p(x). For every time step, the element with the smallest value in the system is selected and renewed by assigning a new value which is drawn from p(x). It is assumed that no two x(i) can take the same value.
For the above system the typical values of x(i) increase monotonically in time. This means that any renewed element is likely to have a smaller x(i) than the bulk, and hence a shorter than average lifespan until it is again renewed. Corresponding, elements that have not been renewed for some time will have a longer than average life expectancy. This separation between the shortest and the longest-lived elements will become more pronounced as the system evolves and the average x(i) in the bulk increases. This phenomenon is called long-time memory.
Extremally driven systems can generally be expected to exhibit long-term memory [1].
In Bee foraging [4] neither do the foragers compare different
nectar sources to determine the relative profitability of any one
source, nor do the food storers compare different nectar loads
and indicate the relative profitability of each load to the foragers.
Instead, each forager knows only about its particular nectar source
and independently calculates the absolute profitability of its source.
Even though each of a colony’s foragers operates with extremely
limited information about the colony’s food sources, together they
will generate a coherent colony level response to different food
sources in which better ones are heavily exploited and poorer ones
are abandoned. This is similar to the idea of extremal optimization.
Proposed algorithm:
a. Every site i has a fitness f(i)=e(i)/n(i) where e(i) is energy
efficiency (energy gained per energy spent ) from it and n(i) is
number of foragers using it.
b. If f(i)>=rnd, where rnd is a random number uniform ally
distributed between [0,1], then n(i) remain the same.
c. If f(i)
We have simulated this algorithm and obtained the following result:
f .070 .228 1 1 1 1 1 1 1 1
n 0 0 1 1 2 3 4 4 4 4
Although the result is mainly monotonic, but some deviations are expected due to the random element of the process. Our results agree with the results of [5].
Recently Covid-19 [6] has caused a problem in medical supplies e.g. masks. This problem is similar to the one studied in sec.2. The flowers correspond to the medical goods suppliers and the bees correspond to their consumers e.g. medical workers and patients. The objective is to reach equitable distribution of users (bees) on producers (flowers). The algorithm in sec. 2 solves this problem
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