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Article

The Uniform Poisson–Ailamujia Distribution: Actuarial Measures and Applications in Biological Science

1
Department of Mathematics & Statistics, College of Science, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia
2
Department of Statistics, Faculty of Science, Selçuk University, Konya 42250, Turkey
3
Departamento de Estatística, Universidade Federal de Pernambuco, Recife 50710-165, Brazil
4
Department of Statistics, Mathematics and Insurance, Benha University, Benha 13511, Egypt
*
Author to whom correspondence should be addressed.
Symmetry 2021, 13(7), 1258; https://doi.org/10.3390/sym13071258
Submission received: 10 June 2021 / Revised: 9 July 2021 / Accepted: 12 July 2021 / Published: 13 July 2021

Abstract

:
We propose a new asymmetric discrete model by combining the uniform and Poisson–Ailamujia distributions using the binomial decay transformation method. The distribution, named the uniform Poisson–Ailamujia, due to its flexibility is a good alternative to the well-known Poisson and geometric distributions for real data applications in public health, biology, sociology, medicine, and agriculture. Its main statistical properties are studied, including the cumulative and hazard rate functions, moments, and entropy. The new distribution is considered to be suitable for modeling purposes; its parameter is estimated by eight classical methods. Three applications to biological data are presented herein.

1. Introduction

Discrete distributions are quite useful for modeling discrete lifetime data in many situations. Recently, several continuous distributions have been discretized for modeling lifetime data, such as those summarized in Table 1.
On the other hand, a natural discrete analog of the continuous Lindley model, called natural discrete Lindley (NDL), was introduced by [8] as a mixture of the negative binomial and geometric distributions. Several reliability properties of the NDL were explored by [9].
Let N and X be two discrete random variables denoting the numbers of particles entering and leaving an attenuator, with their probability mass functions (pmfs) p ( n ) and P ( X = x ) that are connected by the binomial decay transformation introduced by Hu et al. [10]
P ( X = x ) = n = x n x ( 1 p ) n x p x p ( n ) , x = 0 , 1 , ,
where 0 p 1 is the attenuating coefficient. Hu et al. [10] defined p ( n ) as a pmf of a Poisson distribution with rate parameter λ > 0 and illustrated that P ( X = x ) is also a Poisson distribution with rate λ p . They investigated the quantitative relation between the input and output distributions after the attenuation. In recent studies, new discrete models have been constructed by compounding two discrete distributions. For example, Déniz [11] defined the uniform Poisson, Akdoğan et al. [12] proposed the uniform geometric, and Kuş et al. [13] introduced the binomial discrete Lindley.
In this paper, we introduce the asymmetric uniform Poisson–Ailamujia (UPA) distribution using the methodology of Hu et al. [10]. This distribution is a competitor to the Poisson–Ailamujia (PA) model, and it is suitable for fitting datasets with excesses of ones. We estimate the parameter α of the UPA distribution using eight classical methods and provide detailed simulations to explore the behavior of the estimators.
The rest of the paper is organized as follows. Section 2 defines the new one-parameter distribution and some of its properties. Two actuarial measures are calculated in Section 3. The estimation methods are discussed in Section 4. In Section 5, the efficiency of the estimators is studied via Monte Carlo simulations. Section 6 provides three real applications of the new distribution. Section 7 offers some conclusions.

2. The Discrete UPA Distribution

The PA distribution was derived from the Poisson compounding scheme based on the continuous Ailamujia distribution by Lv et al. [14]. It was pioneered by Hassan et al. [15] for modeling count data, offering a new alternative to the Poisson and the negative binomial, among other models. Its pmf has the form (for α > 0 ).
P X = x = 4 α 2 ( 1 + x ) ( 1 + 2 α ) x + 2 , x N .
Equation (2) can be expressed as
P X = x = n = x P N = n P X = x N = n ,
where X | N = n has the binomial B ( n , p ) model. Now, let X | N = n have the discrete uniform U n with parameter n 0 , and let N have a PA distribution with parameter α > 0 . Then, the pmf of the UPA random variable ( r v ), say, X UPA α , is as follows (for x = 0 , 1 , ):
f x = P X = x = n = x 1 ( n + 1 ) 4 α 2 ( 1 + n ) ( 1 + 2 α ) n + 2 = 2 α ( 1 + 2 α ) x + 1 .
Figure 1 displays plots of the pmf of X, which is unimodal. The probabilities of P ( X = x ) decrease when x increases.

2.1. Properties

The survival function (sf) of the UPA distribution is as follows (for x = 0 , 1 , ):
S x = P X x = 1 P X x 1 = 1 i = 0 x 1 2 α ( 1 + 2 α ) i + 1 = 1 ( 1 + 2 α ) x .
The cumulative distribution function (cdf) of X reduces to
F x = P X x = i = 0 x 2 α ( 1 + 2 α ) i + 1 = 1 1 ( 1 + 2 α ) x + 1 , x = 0 , 1 ,
The hazard rate function (hrf) of X can be defined as h x = P X = x X x = P X = x / P X x , where P X x > 0 . Then, the hrf of the UPA distribution follows from Equations (4) and (5) as
h ( x ) = 2 α ( 1 + 2 α ) .
The moment generating function of X is
M X t = E e tX = x = 0 e tx 2 α ( 1 + 2 α ) x + 1 = 2 α 1 + 2 α e t .
The first fourth ordinary moments of X are
E X = 1 2 α , E ( X 2 ) = 1 + α 2 α 2 ,
E ( X 3 ) = 3 + 6 α + 2 α 2 4 α 3 and E ( X 4 ) = 3 + 9 α + 7 α 2 + α 3 2 α 4 .
The variance, skewness, and kurtosis of X are obtained from these expressions as
V a r X = 2 α + 1 4 α 2 , γ 1 X = 2 ( 1 + α ) 1 + 2 α > 0 and γ 2 X = 4 α 2 + 18 α + 9 1 + 2 α > 0 .
We note that the new distribution is over-dispersed since the index of dispersion (ID)
I D = V a r X E X = 2 α 2 α + 1 4 α 2 = 2 α + 1 2 α > 1 .
Hence, the UPA distribution can be used for modeling over-dispersed data. In addition, it is right-skewed and leptokurtic, since γ 1 X   >   0 and γ 2 X   >   0 , respectively. The UPA distribution is a heavy-tailed distribution.
Table 2 gives some moments, variances, and IDs in terms of α . Figure 2 displays the plots of the skewness and kurtosis versus α . The ID decreases monotonically in α , whereas the skewness and kurtosis monotonically increase for α 0 , .

2.2. Stochastic Orders of the Parameter α

Shaked and Shanthikumar [16] showed that some stochastic orders exist and have several applications. Theorem 1 shows that the UPA distribution is ordered according to the strongest stochastic order, namely, the likelihood ratio ( l r ) order.
Definition 1.
Consider the two random variables X and Y with respective pmfs f X ( · ) and f Y ( · ) . Then, X is said to be smaller than Y in the l r order, denoted by X l r Y , if  f X ( x ) / f Y ( x ) is non-decreasing in x.
Theorem 1.
Let X UPA α 1 and Y UPA α 2 . Then X l r Y for all α 1 > α 2 .
Proof. 
We have
L x = f X ( x ) f Y ( x ) = α 1 α 2 1 + 2 α 2 1 + 2 α 1 x + 1
and
L x + 1 = f X ( x + 1 ) f Y ( x + 1 ) = α 1 α 2 1 + 2 α 2 1 + 2 α 1 x + 2 .
Clearly, one can note that
L x + 1 L x = 1 + 2 α 2 1 + 2 α 1 < 1 , α 1 > α 2 .
 □

2.3. Entropy

The Shannon entropy of X can be expressed as
H ( X ) = x = 0 P ( X = x ) log [ P ( X = x ) ] = x = 0 2 α ( 2 α + 1 ) x + 1 log 2 α x + 1 log ( 2 α + 1 ) = 2 α 1 log 2 α + 1 + log 2 α + 1 log 2 α = log 2 α + 1 1 2 α + 1 log 2 α .
Table 3 gives some values of H ( X ) in terms of the parameter α . Figure 3 displays the plot of H ( X ) versus α . The entropy H ( X ) is monotonically decreasing for α 0 , , and it proceeds to zero when α becomes larger.

2.4. Quantile Function

The quantile function (qf) of the UPA distribution is determined by inverting (6) as
Q u = 1 log 1 u log 1 + 2 α .
The ath quantile x a of X can be expressed from Equation (17) as
x a = 1 log 1 u log 1 + 2 α + 1 , Q a Q a 1 log 1 u log 1 + 2 α , 1 log 1 u log 1 + 2 α + 1 , Q a = Q a ,
where x denotes the integer part of x. The quantity x a satisfies F x a p F x a , where F ( x ) is the cdf given in (6). The median of the UPA α distribution is x 0.5 .

3. Actuarial Measures

In this section, we determine the value at risk (VaR) and tail value at risk (TVaR) of the UPA α distribution.

3.1. VaR Measure

Let X denote a loss r v . The VaR p of X at the 100 p % level, say, π p , is the 100 p percentile of the distribution of X, namely,
P X > π p = 1 p , and then π p = F 1 p ,
where p 0 , 1 , and F ( x ) is the cdf of the UPA distribution given in (6). The quantity VaR p of the UPA distribution comes from the qf (17) as follows:
π p = 1 log 1 p log 1 + 2 α .

3.2. TVaR Measure

The TVaR of X at the 100 p % security level, say, TVAR p , has the form
TVAR p = E X X > π p = x = π p x f x 1 F π p .
The TVaR p measure for the UPA α model follows from Equations (4) and (6).
TVAR p = 1 + 2 α 1 + log 1 u log 1 + 2 α 1 2 α log 1 + 2 α 2 α log 1 p 2 α 1 p log 1 + 2 α .
Some VaR p and TVaR p values for the UPA distribution are listed in Table 4.
The figures in Table 4 and the plots in Figure 4 indicate that the VaR and TVaR measures are increasing functions of α .

4. Estimation

In this section, the parameter α is estimated by eight methods, and their performances are investigated via Monte Carlo simulations. The proposed estimators are determined from the maximum likelihood, moments, proportions, ordinary and weighted least-squares, Cramér–von Mises, right-tail Anderson–Darling, and percentiles methods. For all methods, let x 1 , , x n be n independent observations from the UPA distribution.

4.1. Maximum Likelihood

The log-likelihood function for α comes from (4) as follows:
n ( α ) = i = 0 n log [ f ( x i ; α ) ] = n log ( 2 α ) i = 0 n ( x i + 1 ) log ( 1 + 2 α ) .
Then, the maximum likelihood estimate (MLE) of α , say, α ^ , is determined by maximizing n ( α ) with respect to this parameter as the solution of
d n ( α ) d α = n α 2 1 + 2 α i = 0 n ( x i + 1 ) = 0 ,
which gives α ^ = 1 / ( 2 x ¯ ) if x ¯ > 0 , where x ¯ = n 1 i = 1 n x i .
Under some regularity conditions, the distribution of α ^ can be approximated by the N ( α , 1 / I α ^ ) distribution, where I α is the observed Fisher information.
I ( α ) = d 2 n ( α ) d α 2 = n α 2 4 1 + 2 α 2 i = 0 n ( x i + 1 ) .
An asymptotic confidence interval for α at the level ( 1 γ ) 100 % with γ ( 0 , 1 ) has the form
α ^ z γ / 2 1 / I α ^ , α ^ + z γ / 2 1 / I α ^ ,
where z γ / 2 is the ( 1 γ / 2 ) -quantile of the normal N ( 0 , 1 ) distribution.

4.2. Moments

The moment estimate (MOE) α ˜ of α follows from E X given in Section 2.1 as
α ˜ = 1 2 x ¯ ,
if x ¯ > 0 . From the central limit theorem,
n X ¯ μ d N 0 , σ 2 ,
where
μ = 1 2 α and σ 2 = 2 α + 1 4 α 2 .
Based on the delta method,
n p ˜ p d N 0 , 2 α + 1 .
For any 0 < γ < 1 , an approximate 100 1 γ confidence interval for the parameter α comes from (30) as
P α ˜ z γ / 2 S n < α < α ˜ + z γ / 2 S n = 1 γ ,
where S = 2 α ˜ + 1 .

4.3. Proportions

We define the indicator function ν ( · ) (for i = 1 , , n ) as
ν x i = 1 , x i = 0 , 0 , x i > 0 .
Clearly, the proportion y = n 1 i = 1 n ν x i refers to the proportion of zeros in the sample, and it is an unbiased and consistent estimate of the probability
f 0 = 2 α 1 + 2 α .
Then, the proportions estimate (POE) of α [17] follows by solving
y = 2 α 1 + 2 α ,
which leads to the estimate α ^ = y / [ 2 ( y 1 ) ] .

4.4. Ordinary and Weighted Least-Squares

Let X j : n be the jth-order statistic in a sample of size n. We adopt lower cases for sample values. It is well-known that E F ( X j : n ) = j 1 + n and V F ( X j : n ) = j ( n j + 1 ) ( n + 1 ) 2 ( n + 2 ) .
The least-squares estimate (LSE) of α , α ^ , follows by minimizing
j = 1 n 1 1 ( 1 + 2 α ) x j : n + 1 j n + 1 2 ,
in relation to α .
The weighted least-squares estimate (WLSE) of α , α ˜ , is determined by minimizing
j = 1 n ϕ j 1 1 ( 1 + 2 α ) x j : n + 1 j n + 1 2 ,
in relation to α , where the weight function is ϕ j = [ ( n + 1 ) 2 ( n + 2 ) ] / [ j ( n j + 1 ) ] .

4.5. Cramér-von Mises

The Cramér–von Mises estimate (CVME) (see [18,19]) is based on the difference between the estimate of the cdf and its empirical cdf [20]. The CVME of α follows by minimizing
C ( α ) = 1 12 n + j = 1 n 1 1 ( 1 + 2 α ) x j : n + 1 2 j 1 2 n 2 ,
with respect to α . Further, the CVME of α is also obtained by solving
j = 1 n 1 1 ( 1 + 2 α ) x j : n + 1 2 j 1 2 n 2 x j : n + 1 ( 1 + 2 α ) x j : n + 2 = 0 .

4.6. Right-Tail Anderson–Darling

The right-tail Anderson–Darling estimate (RADE) of α follows by minimizing
R ( α ) = n 2 2 j = 1 n 1 1 ( 1 + 2 α ) x j : n + 1 1 n j = 1 n 2 j 1 log 1 1 ( 1 + 2 α ) x n + 1 j : n ,
in relation to α . The RADE of α is also found by solving the equation
4 j = 1 n x j : n + 1 ( 1 + 2 α ) x j : n + 2 + 2 n j = 1 n 2 j 1 x n + 1 j : n + 1 ( 1 + 2 α ) 2 = 0 .

4.7. Percentiles

The percentile estimate (PCE) is obtained by equating the sample percentile point to the population percentile. If p j denotes an estimate of F ( x j : n ; α ) , the PCE of α , say α ^ P C E , follows by minimizing
P ( α ) = j = 1 n x j Q ( p j ) 2 ,
where p j = j 1 + n is an unbiased estimator of F ( x j : n ; α ) and
Q ( p j ) = log 1 + 2 α 1 p j log 1 + 2 α .

5. Simulation Study

We conducted a simulation study to evaluate the accuracy of the eight estimators discussed before. We generated samples of sizes n = 30 , 75 , 100 , 150 , 200 , and 300 from the UPA distribution and then calculated the average values of the MLE, MOE, POE, LSE, WLSE, CVME, RADE, and PCE of α (AVEs), mean square errors (MSEs), average absolute biases (ABBs), and mean relative errors (MREs) when α = 0.35 , 0.5 , 1.5 , and 3.0 . The ABBs, MSEs and MREs are given by
A B B s α ^ = 1 N i = 1 N α ^ α ,
M S E α ^ = 1 N i = 1 N α ^ α 2
and
M R E α ^ = 1 N i = 1 N α ^ α / α .
We repeated the simulation 5000 times to calculate these measures for MLE, MOE, POE, LSE, WLSE, CVME, RADE, and PCE from the previous settings. The results reported in Table 5, Table 6, Table 7 and Table 8 were found using the optim-CG routine of R software.
The numbers in Table 5, Table 6, Table 7 and Table 8 reveal that the AVEs became closer to the true values of α when the sample size n increased, as expected. Further, the ABBs, MREs, and MSEs for all estimators decreased when n increased. Moreover, the MLE and MOE were the best estimators under these criteria. The MLE and MOE were almost identical in terms of the ABBs, MSEs, and MREs, and both had better performances than the other estimators. Additionally, the biases and MSEs of all estimators decayed toward zero when n increased. In summary, the performance ordering of the proposed estimators, from best to worst, was MLE, MOE, WLSE, LSE, POE, PCE, RADE, and CVME. Hence, maximum likelihood was adopted for the work in the next section.

6. Modeling Biological Data

In this section, the UPA distribution is fitted to three real biological datasets and compared with the discrete Burr–Hatke (DBH) [21], discrete Poisson Lindley (DPL) [22], natural discrete Lindley (NDL) [8], discrete Pareto (DP) [5], PA and Poisson distributions according to the model’s ability. The first dataset (Catcheside et al. [23]) refers to numbers of chromatid aberrations, and it was adopted by Hassan et al. [15] for comparing the Poisson and PA distributions. We aimed to test whether the UPA model is a more reasonable choice for these data based on the chi-squared test. Under the null hypothesis, the estimated probabilities were
α i ^ = P ^ ( X = i ) = 2 α ^ ( 1 + 2 α ^ ) i + 1 , i = 0 , 1 .
The estimated expected frequencies were e i ^ = n α i ^ . The results of the chi-square test were reported in Table 9 considering five cells, where
χ 2 = i = 1 5 ( o i e i ^ ) 2 e i ^ = 4.2507 < χ 0.95 2 ( 4 ) = 9.4877 ,
where e i ^ and o i are, respectively, the expected and observed frequencies for x = i . Thus, we cannot reject H 0 at the 5% significance level, and then the UPA distribution is quite suitable for these data.
We also report in Table 9 the results of the χ 2 test for the UPA and other distributions based on the MLE of α . The UPA distribution provided the best fit since it resulted in the smallest χ 2 value. This conclusion can also be confirmed by the log-likelihood test. Figure 5 displays the empirical pmf and seven pmfs fitted to the first dataset, which confirm that the new distribution yielded the best fit to the current data.
The second dataset (Catcheside et al. [23]) represents the number of mammalian cytogenetic dosimetry lesions in rabbit lymphoblasts induced by streptonigrin (NSC-45383) exposure—70 3bc g/kg. We fitted the UPA and other distributions to these data.
Table 10 reports the results of the χ 2 test for seven fitted distributions, and Figure 6 displays the empirical pmf and seven pmfs fitted to these data. We have
χ 2 = i = 1 5 ( o i e i ^ ) 2 e i ^ = 4.9000 < χ 0.95 2 ( 4 ) = 9.4877 .
Then, the hypothesis H 0 : X UPA ( α ) cannot be rejected at the 5% significance level. Thus, the UPA distribution is a reasonable model for these data.
Based on the χ 2 tests, log-likelihood values, and Figure 6, we conclude that the UPA model provided a better fit for the second dataset than the other distributions.
The third dataset refers to counts of daily new COVID-19 deaths of Switzerland between 1 March to 30 June 2021 available at https://github.com/owid/COVID-19-data/tree/master/public/data/ (accessed on 6 July 2021). We adopt these data to show the flexibility of the UPA model comparing to other models based on three criteria: Akaike information criterion (AIC), Bayesian information criterion (BIC), and −maximized log-likelihood ( ^ ). These daily new deaths are: 22, 17, 9, 8, 19, 5, 2, 8, 9, 17, 8, 14, 4, 4, 6, 29, 16, 20, 20, 0, 10, 26, 8, 29, 8, 14, 1, 1, 5, 17, 15, 13, 1, 0, 2, 24, 26, 29, 13, 5, 2, 1, 13, 6, 16, 10, 7, 0, 3, 13, 11, 14, 9, 11, 28, 13, 8, 26, 8, 7, 1, 1, 21, 12, 18, 10, 7, 2, 2, 9, 6, 4, 3, 2, 0, 1, 13, 8, 4, 4, 8, 7, 1, 3, 7, 3, 9, 3, 4, 1, 4, 16, 0, 2, 3, 1, 0, 9, 3, 7, 2, 6, 0, 0, 2, 5, 2, 0, 1, 0, 0, 7, 0, 0, 4, 2, 0, 0, 3, 2, 4. The Kolmogorov–Smirnov statistic for the UPA model is 0.1132 with a p-value of 0.0920 .
Table 11 reports the estimates of α , and the values of AIC, BIC and ^ for the UPA and other distributions. According to the figures in this table, the UPA distribution is more adequate for these data than the DPL, NDL, DPL, PA, DP, DBH, and Poisson distributions. This conclusion is also supported by Figure 7.
Some useful probabilities can be easily calculated from the estimated cdf. For example, a researcher would like to know the risk that more than ten deaths occur in Switzerland in just one day during that coronavirus period.

7. Conclusions

New discrete distributions are very important for modeling real-life scenarios since the traditional ones have limited applications in failure times, reliability, counts, etc. We proposed and studied the uniform Poisson–Ailamujia (UPA) distribution, which can give better fits than other discrete distributions, especially when modeling over-dispersed count data. Seven methods were discussed to estimate its parameter, and Monte Carlo simulations showed that the maximum likelihood and moments are the best ones. The flexibility of the UPA model was proven empirically by means of three real biological datasets. Furthermore, the UPA distribution can be extended in some ways. For example, the transmuted UPA, exponentiated UPA, Beta UPA, Kumaraswamy UPA can be defined to provide more flexibility with two and three parameters and to increase the potential applicability of the UPA distribution. It is difficult, sometimes, to measure lifetimes or counts on a continuous scale. In practice, we come across situations, where lifetimes are discrete random variables. For example, the number of days that COVID-19 patients stay in hospital beds, the number of hospital beds occupied by coronavirus patients in a hospital, the number of comorbidities in these patients, etc. We point out examples of epidemiology, but it can be applied in several other areas.

Author Contributions

Conceptualization, Y.A. and G.M.C.; methodology, Y.A. and A.Z.A.; software, Y.A.; writing—original draft preparation, Y.A. and A.Z.A.; writing—review and editing, H.M.A., G.M.C. and A.Z.A.; project administration, H.M.A. and A.Z.A.; funding acquisition, H.M.A. All authors have read and agreed to the published version of the manuscript.

Funding

This study was funded by Taif University Researchers Supporting Project number (TURSP-2020/279), Taif University, Taif, Saudi Arabia.

Acknowledgments

The authors would like to thank the Editorial Board and three anonymous reviewers for their constructive comments that greatly improved the final version of the paper.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Pmf of the UPA α distribution for some values of α .
Figure 1. Pmf of the UPA α distribution for some values of α .
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Figure 2. Skewness and kurtosis of the UPA α distribution.
Figure 2. Skewness and kurtosis of the UPA α distribution.
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Figure 3. Entropy of the UPA α distribution.
Figure 3. Entropy of the UPA α distribution.
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Figure 4. Plots of the VaR and TVaR measures for the UPA α distribution.
Figure 4. Plots of the VaR and TVaR measures for the UPA α distribution.
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Figure 5. Fitted and empirical distributions for the first dataset.
Figure 5. Fitted and empirical distributions for the first dataset.
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Figure 6. Fitted and empirical distributions for the second dataset.
Figure 6. Fitted and empirical distributions for the second dataset.
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Figure 7. Empirical and estimated cdf of the UPA distribution for the third dataset.
Figure 7. Empirical and estimated cdf of the UPA distribution for the third dataset.
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Table 1. Some discretized continuous distributions.
Table 1. Some discretized continuous distributions.
Continuous DistributionDiscrete DistributionAuthor
WeibullDiscrete WeibullNakagawa and Osaki [1]
Inverse WeibullDiscrete inverse WeibullStein and Dattero [2]
Normal and RayleighDiscrete normal and RayleighRoy [3,4]
Burr XII and ParetoDiscrete Burr XII and ParetoKrishna and Pundir [5]
GammaDiscrete gammaChakraborty and Chakravarty [6]
ChenDiscrete ChenNoughabi et al. [7]
Table 2. Moments and ID of the UPA α distribution.
Table 2. Moments and ID of the UPA α distribution.
α MeanB E X 2 E X 3 E X 4 ID
0.252.00006.000010.000074.0000730.00003.0000
0.750.66671.11111.55555.111122.29631.6667
1.000.50000.75001.00002.750010.00001.5000
1.250.40000.56000.72001.74405.55841.4000
1.500.33330.44440.55551.22223.51851.3333
1.750.28570.36730.44900.91542.42811.2857
2.000.25000.31250.37500.71871.78121.2500
2.250.22220.27160.32100.58441.36721.2222
2.500.20000.24000.28000.48801.08641.2000
2.750.18180.21490.24790.41620.88721.1818
3.250.15380.17750.20110.31770.62971.1538
3.750.13330.15110.16890.25420.47511.1333
4.500.11110.12340.13580.19340.33701.1111
5.500.09090.09920.10740.14500.23531.0909
7.500.06670.07110.07550.09510.14001.0667
9.500.05260.05540.05820.07010.09681.0526
10.000.05000.05250.05500.06570.08961.0500
50.000.01000.01010.01020.01060.01141.0100
75.000.00670.00670.00670.00690.00731.0067
100.000.00500.00500.00500.00510.00531.0050
Table 3. Entropy of the UPA α distribution.
Table 3. Entropy of the UPA α distribution.
α H ( X ) α H ( X ) α H ( X )
3.50.430670.2624
0.51.386340.39247.50.2494
10.95484.50.361280.2377
1.50.749850.33518.50.2272
20.62555.50.312990.2176
2.50.540760.29389.50.2090
30.47856.50.2771100.2010
Table 4. The VaR and TVaR measures for the UPA α model.
Table 4. The VaR and TVaR measures for the UPA α model.
α Security Level VaR p TVaR p
0.250.80 2.9694 7.4074
0.85 3.6789 7.9012
0.90 4.6789 9.2181
0.95 6.3884 10.5350
0.99 10.3577 15.0293
0.50.80 1.3219 4.6338
0.85 1.7369 5.4739
0.90 2.3219 6.6438
0.95 3.3219 8.6438
0.99 5.6438 13.2877
1.50.80 0.1610 1.9772
0.85 0.3685 2.8073
0.90 0.6610 3.9772
0.95 1.1610 5.9772
0.99 2.3219 10.6210
Table 5. Simulation results of the UPA model for α = 0.35 .
Table 5. Simulation results of the UPA model for α = 0.35 .
n MLEPOEMOELSEWLSECVMERADEPCE
30AVEs0.35710.33330.35710.36330.36350.37540.37420.3724
MSEs0.30310.00760.00310.00390.00400.02050.01980.0764
ABSs0.05540.08750.05540.06260.06310.08630.07890.2624
MREs0.15830.25040.15830.17880.18040.24150.14280.8639
75AVEs0.35050.35230.35050.35550.35570.34950.34650.3639
MSEs0.00130.00270.00130.00170.00180.01010.00870.0458
ABSs0.03660.05210.03660.04150.04210.07740.07120.2139
MREs0.10460.14890.10460.11840.12040.22120.07120.6112
100AVEs0.35210.34740.35210.35250.35210.33940.34160.3480
MSEs0.00100.00190.00100.00130.00130.00570.00500.0065
ABSs0.03150.04350.03150.03550.03600.06020.05570.0634
MREs0.09010.12440.09080.10170.10290.17190.05570.1812
150AVEs0.35050.35230.35050.35240.35240.33970.34030.3478
MSEs0.00060.00180.00060.00080.00080.00450.00390.0049
ABSs0.02500.04280.02500.02910.02940.05370.04980.0556
MREs0.07140.12240.07140.08320.08410.15350.04980.1589
200AVEs0.35090.34740.35080.35250.35250.33540.33890.3418
MSEs0.00050.00120.00050.00060.00060.00230.00200.0024
ABSs0.02170.03490.02170.02470.02480.03920.03600.0393
MREs0.06210.09990.06210.07070.07100.11210.03600.1123
300AVEs0.35050.35220.35050.35190.35160.34630.34650.3488
MSEs0.00030.00070.00030.00040.00040.00100.00080.0009
ABSs0.01760.02720.01760.02030.02040.02610.02260.0236
MREs0.05040.07770.05040.05790.05830.07450.02260.0673
Table 6. Simulation results of the UPA model for α = 0.5 .
Table 6. Simulation results of the UPA model for α = 0.5 .
n MLEPOEMOELSEWLSECVMERADEPCE
30AVEs0.51720.51270.51720.51460.51550.47570.47850.4898
MSEs0.00690.01380.00690.00890.00890.01670.01470.0217
ABBs0.08330.11760.08330.09430.09440.10280.09670.1136
MREs0.16670.23530.16670.18860.18880.20500.19340.2273
75AVEs0.51450.48680.51450.50200.50160.46530.47130.4848
MSEs0.00290.00510.00290.00370.00380.00730.00600.0077
ABBs0.05360.07140.05360.06120.06150.07030.06340.0704
MREs0.10710.14290.10710.12240.12300.14070.12670.1408
100AVEs0.51260.48680.51270.50200.50160.46190.45880.4871
MSEs0.00240.00410.00240.00290.00290.00560.00450.0059
ABBs0.04950.06380.04950.05420.05420.06200.05620.0615
MREs0.09890.12770.09890.10850.10850.12410.11240.1230
150AVEs0.50980.50570.50970.50230.50190.45880.46780.4894
MSEs0.00160.00320.00160.00200.00190.00450.00360.0040
ABBs0.03960.05630.03960.04470.04410.05620.04970.0508
MREs0.07910.11270.07910.08940.8830.11240.09930.1016
200AVEs0.50440.50050.50450.50110.50080.46000.46650.4906
MSEs0.00110.00230.00110.00140.00140.00370.00300.0030
ABBs0.03270.04760.03270.03790.03790.05100.04560.0442
MREs0.06540.09520.06540.07550.07580.10210.09110.0883
300AVEs0.50050.50040.50040.50030.50030.45730.46670.4914
MSEs0.00080.00150.00080.00100.00100.00310.00240.0019
ABBs0.02820.03850.02820.03120.03150.04800.04060.0354
MREs0.05630.07690.05630.06250.06300.09610.08130.0708
Table 7. Simulation results of the UPA model for α = 1.5 .
Table 7. Simulation results of the UPA model for α = 1.5 .
n MLEPOEMOELSEWLSECVMERADEPCE
30AVEs1.54211.64291.55211.60691.60441.18871.20151.5306
MSEs0.14060.25000.14060.20600.20290.23160.22031.0837
ABBs0.37500.50240.37500.45380.45040.41600.40450.4863
MREs0.25000.33330.25010.30250.30030.27730.26960.3241
75AVEs1.52151.47371.52571.49921.49411.13891.16121.4721
MSEs0.04280.08730.04280.06040.06170.17500.15940.1434
ABBs0.20690.29550.20690.24570.24830.37800.35980.2931
MREs0.13790.19700.13790.16380.16560.25200.23990.1954
100AVEs1.51521.52471.51521.50291.50281.13371.16411.4760
MSEs0.04750.04590.04750.04690.04700.16760.14500.1075
ABBs0.21790.21430.21790.21660.21690.37480.34710.2555
MREs0.14530.14290.14530.14440.14460.24990.23140.1703
150AVEs1.51581.52701.52471.51101.51201.13051.16001.4791
MSEs0.02780.04240.02780.03480.03470.15750.13640.0069
ABBs0.16670.20590.16670.18650.18620.37140.34310.2073
MREs0.11110.13730.11110.12430.12410.24760.228801382
200AVEs1.51521.51231.51521.50001.49951.12111.15221.4794
MSEs0.02210.03020.02200.02650.02650.15900.13060.0494
ABBs0.14860.17390.14860.16270.16290.37950.34790.1778
MREs0.09910.11590.09910.10840.10860.25300.23300.1186
300AVEs1.50451.50571.50981.50321.50281.12051.15221.4813
MSEs0.01270.01560.01270.01600.01590.15430.13060.0329
ABBs0.11290.12500.11290.12650.12600.37660.34790.1452
MREs0.07530.08330.07520.08440.08400.25310.23190.0968
Table 8. Simulation results of the UPA model for α = 3.0 .
Table 8. Simulation results of the UPA model for α = 3.0 .
n MLEPOEMOELSEWLSECVMERADEPCE
30AVEs3.42703.25003.23473.23663.28662.50012.50303.4441
MSEs0.73471.01240.73471.04171.02481.57881.59041.8639
ABBs0.85711.01470.85711.02061.01231.13591.12751.4804
MREs0.28570.33330.28570.34020.33740.37860.37580.4935
75AVEs3.12502.90913.12502.93392.93642.88592.91323.0907
MSEs0.43070.44440.43070.43020.43041.40551.33841.2770
ABBs0.65620.66670.65630.65600.65611.12361.09630.7931
MREs0.21880.22220.21880.21870.21870.37450.36540.2644
100AVEs3.12503.07143.12503.07113.07112.86422.89883.0839
MSEs0.32650.31220.32650.33180.32891.40621.32430.8779
ABBs0.57140.55880.57140.57600.57351.13881.10450.6850
MREs0.19050.18630.19050.19200.19120.37960.36810.2283
150AVEs3.07853.07143.06733.06503.06562.85132.88923.0408
MSEs0.17120.20010.17120.20260.20311.39061.30210.5301
ABBs0.41380.44740.41380.45020.45071.14871.11090.5437
MREs0.13790.14910.13790.15000.15020.38290.37030.1819
200AVEs3.03033.07143.03033.05783.05622.84702.88043.0547
MSEs0.13570.14060.13570.14390.14491.38201.30470.3779
ABBs0.36840.37500.36840.37940.38071.15301.11970.4726
MREs0.12280.12500.12280.12650.12690.38440.37320.1576
300AVEs3.01592.98843.01582.99232.99172.84122.87653.0507
MSEs0.10330.11980.10330.11780.11831.37851.29450.2502
ABBs0.32140.34620.32140.34320.34391.15881.12350.3854
MREs0.10710.11540.10710.11440.11460.38630.37450.1285
Table 9. Results of the χ 2 test for the first dataset.
Table 9. Results of the χ 2 test for the first dataset.
CountObservedExpected
UPADBHNDLPoissonParetoPADPL
0268264.03282.33258.76238.99292.41252.96262.44
18789.7571.5295.87123.0957.68103.6091.61
22630.5125.7931.5731.7020.9731.8230.92
3910.3710.789.755.449.988.6910.19
4103.534.892.890.705.542.223.30
Total n = 400
Parameters α ^ 0.97090.58830.75300.51500.15041.94172.5012
χ 2 5.336.497.5429.4115.1711.375.94
^ 388.44389.76390.99408.63405.12392.55388.74
Table 10. Results of the χ 2 test for the second dataset.
Table 10. Results of the χ 2 test for the second dataset.
CountObservedExpected
UPADBHNDLPoissonParetoPADPL
0200195.80209.55190.60174.83216.88186.00193.45
15768.3154.0973.0794.4043.8979.0969.82
23024.9619.9224.9025.4916.2025.2224.34
378.418.517.964.597.807.158.28
4≥63.063.952.440.624.371.902.76
Total n = 300
Parameters α ^ 0.92590.60300.74440.54000.15701.85182.4002
χ 2 4.905.028.0834.0411.3213.106.15
^ 299.31301.70300.16314.23312.94302.41302.41
Table 11. Estimates, AIC, BIC, and ^ for the third dataset.
Table 11. Estimates, AIC, BIC, and ^ for the third dataset.
Model α ^ AIC BIC
UPA0.0585757.2386757.3214377.6193
DPL0.2318765.8140765.8968381.9070
NDL0.1901767.1740767.2568382.5870
PA0.1275778.3318778.4146388.1659
DP0.5857849.9678850.0506423.9839
DBH0.9920909.8294910.0438452.9147
Poisson7.84301260.36501260.4478629.1825
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Aljohani, H.M.; Akdoğan, Y.; Cordeiro, G.M.; Afify, A.Z. The Uniform Poisson–Ailamujia Distribution: Actuarial Measures and Applications in Biological Science. Symmetry 2021, 13, 1258. https://doi.org/10.3390/sym13071258

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Aljohani HM, Akdoğan Y, Cordeiro GM, Afify AZ. The Uniform Poisson–Ailamujia Distribution: Actuarial Measures and Applications in Biological Science. Symmetry. 2021; 13(7):1258. https://doi.org/10.3390/sym13071258

Chicago/Turabian Style

Aljohani, Hassan M., Yunus Akdoğan, Gauss M. Cordeiro, and Ahmed Z. Afify. 2021. "The Uniform Poisson–Ailamujia Distribution: Actuarial Measures and Applications in Biological Science" Symmetry 13, no. 7: 1258. https://doi.org/10.3390/sym13071258

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Aljohani, H. M., Akdoğan, Y., Cordeiro, G. M., & Afify, A. Z. (2021). The Uniform Poisson–Ailamujia Distribution: Actuarial Measures and Applications in Biological Science. Symmetry, 13(7), 1258. https://doi.org/10.3390/sym13071258

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