In this paper, we compare the entropy of the original distribution and its corresponding compound distribution. Several results are established based on convex order and relative log-concave order. The necessary and sufficient condition for a compound distribution to be log-concave is also discussed, including compound geometric distribution, compound negative binomial distribution and compound binomial distribution.

This paper studies a special type of binomial splitting process. Such a process can be used to model a high dimensional corner parking problem as well as determining the depth of random PATRICIA (practical algorithm to retrieve information coded in alphanumeric) tries, which are a special class of digital tree data structures. The latter also has natural interpretations in terms of distinct values in independent and identically distributed geometric random variables and the occupancy problem in urn models. The corresponding distribution is marked by a logarithmic mean and a bounded variance, which is oscillating, if the binomial parameter p is not equal to ½, and asymptotic to one in the unbiased case. Also, the limiting distribution does not exist as a result of the periodic fluctuations.

For several pairs (P, Q) of classical distributions on ℕ0, we show that their stochastic ordering P ≤stQ can be characterized by their extreme tail ordering equivalent to P({k*})/Q({k*}) ≥ 1 ≥ limk→k*P({k})/Q({k}), with k* and k* denoting the minimum and the supremum of the support of P + Q, and with the limit to be read as P({k*})/Q({k*}) for finite k*. This includes in particular all pairs where P and Q are both binomial (bn1,p1 ≤stbn2,p2 if and only if n1 ≤ n2 and (1 - p1)n1 ≥ (1 - p2)n2, or p1 = 0), both negative binomial (b−r1,p1 ≤stb−r2,p2 if and only if p1 ≥ p2 and p1r1 ≥ p2r2), or both hypergeometric with the same sample size parameter. The binomial case is contained in a known result about Bernoulli convolutions, the other two cases appear to be new. The emphasis of this paper is on providing a variety of different methods of proofs: (i) half monotone likelihood ratios, (ii) explicit coupling, (iii) Markov chain comparison, (iv) analytic calculation, and (v) comparison of Lévy measures. We give four proofs in the binomial case (methods (i)-(iv)) and three in the negative binomial case (methods (i), (iv), and (v)). The statement for hypergeometric distributions is proved via method (i).

Field experiments were conducted in Chile and western Canada to measure short-distance (0 to 100 m) outcrossing from transgenic safflower (Carthamus tinctorius L.) intended for plant molecular farming to non-transgenic commodity safflower of the same variety. The transgenic safflower used as the pollen source was transformed with a construct for seed-specific expression of a high-value protein and constitutive expression of a gene conferring resistance to the broad-spectrum herbicide glufosinate. Progeny of non-transgenic plants grown in plots adjacent to the transgenic pollen source were screened for glufosinate resistance to measure outcrossing frequency. Outcrossing frequency differed among locations: values closest to the transgenic pollen source (0 to 3 m) ranged from 0.48 to 1.67% and rapidly declined to between 0.0024 to 0.03% at distances of 50 to 100 m. At each location, outcrossing frequency was spatially heterogeneous, indicating insects or wind moved pollen asymmetrically. A power analysis assuming a binomial distribution and a range of alpha values (type 1 error) was conducted to estimate an upper and lower confidence interval for the probable transgenic seed frequency in each sample. This facilitated interpretation when large numbers of seeds were screened from the outcrossing experiments and no transgenic seeds were found. This study should aid regulators and the plant molecular farming industry in developing confinement strategies to mitigate pollen mediated gene flow from transgenic to non-transgenic safflower.

We present a method to obtain both exact values and sharp estimates for the total variation distance between binomial and Poisson distributions with the same mean λ. We give a simple efficient algorithm, whose complexity order is to compute exact values. Such an algorithm can be further simplified for moderate sample sizes n, provided that λ is neither close to from the left nor close to from the right. Sharp estimates, better than other known estimates in the literature, are also provided. The 0s of the second Krawtchouk and Charlier polynomials play a fundamental role.

Nanosystems are devices that are in the size range of a billionth of a meter (1 x 10-9) and therefore are built necessarily from individual atoms. The one-dimensional nanosystems or linear nanosystems cover all the nanosized systems which possess one dimension that exceeds the other two dimensions, i.e. extension over one dimension is predominant over the other two dimensions. Here only two of the dimensions have to be on the nanoscale (less than 100 nanometers). In this paper we consider the structural relationship between a linear nanosystem and its atoms acting as components of the nanosystem. Using such information, we then assess the nanosystem's limiting reliability which is, of course, probabilistic in nature. We consider the linear nanosystem at a fixed moment of time, say the present moment, and we assume that the present state of the linear nanosystem depends only on the present states of its atoms.

When detecting the adventitious presence of transgenic plants (AP), it is important to use an appropriate testing method in the laboratory. Dorfman's group testing method is effective for reducing the number of laboratory analyses, but does not consider the case where AP is diluted below the sensitivity of the analyses, which causes the rate of false negatives to increase. The objective of this study is to propose binomial and negative binomial probabilistic models for determining the required sample size (n), number of pools (g), and size of the pool (k) for detecting individuals possessing AP with a probability ≥ (1 − α) (for a small α) given: (1) pool size (k); (2) estimated proportion of individuals with AP in the population (p); (3) concentration of the trait of interest (AP) in individual seeds (w); and (4) detection limit of the test (c) (AP concentration in a pool below which it cannot be detected). The proposed models consider the different rates of false positives (δ) and false negatives (λ), and the assessment of consumer and producer risks. Results have shown that when using the negative binomial, a required sample size n can be determined that guarantees a high probability that m individuals or g pools containing AP will be found. The pools formed have an optimum size, such that one element with AP will be detected at a low cost. The negative binomial distribution should be used when it is known that the proportion of individuals with AP in the population is p < 0.1; thus, it is guaranteed that m individuals or g pools of individuals with AP will be detected with high probability.

Recently, several authors have studied the transient and the equilibrium behaviour of stochastic population processes with total catastrophes. These models are reasonable for modelling populations that are exposed to extreme disastrous phenomena. However, under mild disastrous conditions, the appropriate model is a stochastic process subject to binomial catastrophes. In the present paper we consider a special such model in which a population evolves according to a compound Poisson process and catastrophes occur according to a renewal process. Every individual of the population survives after a catastrophe with probability p, independently of anything else, i.e. the population size is reduced according to a binomial distribution. We study the equilibrium distribution of this process and we derive an algorithmic procedure for its approximate computation. Bounds on the error of this approximation are also included.

Stratified and simple random sampling (or testing) are two common methods used to investigate the number or proportion of items in a population with a particular attribute. Although it is known that cost factors and information about the strata in the population are often crucial in deciding whether to use stratified or simple random sampling in a given situation, the stochastic precedence ordering for random variables can also provide the basis for an interesting criteria under which these methods may be compared. It may be particularly relevant when we are trying to find as many special items as possible in a population (for example individuals with a disease in a country). Properties of this total stochastic order on the class of random variables are discussed, and necessary and sufficient conditions are established which allow the comparison of the number of items of interest found in stratified random sampling with the number found in simple random sampling in the stochastic precedence order. These conditions are compared with other results established on stratified and simple random sampling (testing) using different stochastic-order-type criteria, and applications are given for the comparison of sums of Bernoulli random variables and binomial distributions.

In this paper, we consider the total variation distance between the distributions of two random sums SM and SN with different random summation indices M and N. We derive upper bounds, some of which are sharp. Further, bounds with so-called magic factors are possible. Better results are possible when M and N are stochastically or stop-loss ordered. It turns out that the solution of this approximation problem strongly depends on how many of the first moments of M and N coincide. As approximations, we therefore choose suitable finite signed measures, which coincide with the distribution of the approximating random sum SN if M and N have the same first moments.

We examine how the binomial distribution B(n,p) arises as the distribution Sn = ∑i=1nXi of an arbitrary sequence of Bernoulli variables. It is shown that B(n,p) arises in infinitely many ways as the distribution of dependent and non-identical Bernoulli variables, and arises uniquely as that of independent Bernoulli variables. A number of illustrative examples are given. The cases B(2,p) and B(3,p) are completely analyzed to bring out some of the intrinsic properties of the binomial distribution. The conditions under which Sn follows B(n,p), given that Sn-1 is not necessarily a binomial variable, are investigated. Several natural characterizations of B(n,p), including one which relates the binomial distributions and the Poisson process, are also given. These results and characterizations lead to a better understanding of the nature of the binomial distribution and enhance the utility.

In applied probability, the distribution of a sum of n independent Bernoulli random variables with success probabilities p1,p2,…, pn is often approximated by a Poisson distribution with parameter λ = p1 + p2 + pn. Popular bounds for the approximation error are excellent for small values, but less efficient for moderate values of p1,p2,…,pn.

Upper bounds for the total variation distance are established, improving conventional estimates if the success probabilities are of medium size. The results may be applied directly, e.g. to approximation problems in risk theory.

Some characterizations of continuous and discrete exponential families of distributions are given. These characterizations are used to obtain some limit theorems.