We consider two classes of irreducible Markovian arrival processes specified by the matrices C and D: the Markov-modulated Poisson process (MMPP) and the Markov-switched Poisson process (MSPP). The former exhibits a diagonal matrix D while the latter exhibits a diagonal matrix C. For these two classes we consider the following four statements: (I) the counting process is overdispersed; (II) the hazard rate of the event-stationary interarrival time is nonincreasing; (III) the squared coefficient of variation of the event-stationary process is greater than or equal to one; (IV) there is a stochastic order showing that the time-stationary interarrival time dominates the event-stationary interarrival time. For general MSPPs and order two MMPPs, we show that (I)–(IV) hold. Then for general MMPPs, it is easy to establish (I), while (II) is shown to be false by a counter-example. For general simple point processes, (III) follows from (IV). For MMPPs, we conjecture that (IV) and thus (III) hold. We also carry out some numerical experiments that fail to disprove this conjecture. Importantly, modelling folklore has often treated MMPPs as “bursty”, and implicitly assumed that (III) holds. However, to the best of our knowledge, proving this is still an open problem.

Many seed quality tests are conducted by first randomly assigning seeds into replicates of a given size. The replicate results are then used to check whether or not any problems occur in the realization of the test. The two main tools developed for this verification are the ratio of the observed variance of the replicate results to a theoretical variance and the tolerance for the range of the results. In this paper, we derive the theoretical distribution and its related properties of the sequence of numbers of seeds with a given quality attribute present in the replicates. From these theoretical results, we revisit the two quality checking tools widely used for the germination test. We show a precaution to be taken when relying on the variance ratio to check for under- or over-dispersion of the replicate results. This has led to the development of tables providing credible intervals of the variance ratio. The International Seed Testing Association tolerance tables for the range of the results are also compared with tolerances computed from the exact theoretical distribution of the range, leading us to recommend a revision of these tables.

Mortality data are often classified by age at death and year of death. This classification results in a heterogeneous risk set and this can cause problems for the estimation and forecasting of mortality. In the modelling of such data, we replace the classical assumption that the numbers of claims follow the Poisson distribution with the weaker assumption that the numbers of claims have a variance proportional to the mean. The constant of proportionality is known as the dispersion parameter and it enables us to allow for heterogeneity; in the case of insurance data the dispersion parameter also allows for the presence of duplicates in a portfolio. We use both the quasi-likelihood and the extended quasi-likelihood to estimate models for the smoothing and forecasting of mortality tables jointly with smooth estimates of the dispersion parameters. We present three main applications of our method: first, we show how taking account of dispersion reduces the volatility of a forecast of a mortality table; second, we smooth mortality data by amounts, ie, when deaths are amounts claimed and exposed-to-risk are sums assured; third, we present a joint model for mortality by lives and by amounts with the property that forecasts by lives and by amounts are consistent. Our methods are illustrated with data from the Continuous Mortality Investigation.

This paper describes patterns of infection with Opisthorchis viverrini within a human community assessed by egg count, parasite-specific antibody levels and worm burden determined by expulsion chemotherapy. All three measurements increased significantly with age, reaching a plateau in young adults. There were no significant sex-associated differences in the prevalence or intensity of infection, antibody levels, or in the frequency of heavy worm burdens. A striking 81·5% of the total Opisthorchis population and 74% of the total egg output were expelled by the most heavily infected 10% of the humans sampled. This extreme over-dispersion, together with recent findings that hepatobiliary disease frequently accompanies heavy infections, argues that the priority for community-based parasite control programmes should be to maximize treatment and health promotion efforts toward heavily infected individuals.