The life distribution of a device subject to shocks governed by a homogeneous Poisson process is shown to have a bathtub failure rate average (BFRA) when the probabilities $\bar{P}_k$ of surviving k shocks possess the corresponding discrete property. We prove closure under the formation of weak limits for BFRA distributions and explore related moment convergence issues within the BFRA family. Similar results for increasing and decreasing failure rate average distributions are obtained either independently or as consequences of our results. We also establish some results outlining the positions of various non-monotonic ageing classes such as bathtub failure rate, increasing initially then decreasing mean residual life, new worse then better than used in expectation, and increasing initially then decreasing mean time to failure in the hierarchy. Finally, an open problem is posed and a partial solution provided.

Phylogenetic relationships within the Capsalidae (Monogenea) were examined using large subunit ribosomal DNA sequences from 17 capsalid species (representing 7 genera, 5 subfamilies), 2 outgroup taxa (Monocotylidae) plus Udonella caligorum (Udonellidae). Trees were constructed using maximum likelihood, minimum evolution and maximum parsimony algorithms. An initial tree, generated from sequences 315 bases long, suggests that Capsalinae, Encotyllabinae, Entobdellinae and Trochopodinae are monophyletic, but that Benedeniinae is paraphyletic. Analyses indicate that Neobenedenia, currently in the Benedeniinae, should perhaps be placed in a separate subfamily. An additional analysis was made which omitted 3 capsalid taxa (for which only short sequences were available) and all outgroup taxa because of alignment difficulties. Sequence length increased to 693 bases and good branch support was achieved. The Benedeniinae was again paraphyletic. Higher-level classification of the Capsalidae, evolution of the Entobdellinae and issues of species identity in Neobenedenia are discussed.

Schistosomes are digenean flukes, parasitic of birds, mammals and crocodiles. The family Schistosomatidae contains species of considerable medical and veterinary importance, which cause the disease schistosomiasis. Previous studies, both morphological and molecular, which have provided a good deal of information on the phylogenetics of this group, have been limited in the number of species investigated or the type or extent of molecular data used. This paper presents the most comprehensive phylogeny to date, based on the sequences of 3 genes, complete ribosomal small subunit rRNA and large ribosomal subunit rRNA, and mitochondrial cytochrome oxidase 1, sequenced from 30 taxa including at least 1 representative from 10 of the 13 known genera of the Schistosomatidae and 17 of the 20 recognized Schistosoma species. The phylogeny is examined using morphological characters, intermediate and definitive host associations and biogeography. Theories as to the origins and spread of Schistosoma are also explored. The principal findings are that Ornithobilharzia and Austrobilharzia form a sister group to the Schistosoma; mammalian schistosomes appear paraphyletic and 2 Trichobilharzia species, T. ocellata and T. szidati, seem to be synonymous. The position of Orientobilharzia within the Schistosoma is confirmed, as is an Asian origin for the Schistosoma, followed by subsequent dispersal through India and Africa.

Several interrelationships are apparent between egg weight, chick weight, chick growth and other parameters. The hatchability of intermediate size eggs is better than that of very large or very small eggs. Decreased hatchability, hatchling weight, chick growth and chick viability have been associated with the first few eggs produced by young pullets. Incubation time is positively correlated with egg size. Embryo weight is not correlated with egg weight during the first half of the incubation period. Thereafter the correlation increases and reaches a maximum at the time of hatching (0.5–0.95). Chick weight is primarily determined by initial egg weight, normally being 62–78% of egg weight, and is secondarily determined by weight loss during incubation, shell and residue weight, strain, incubation time and conditions, breeder age and chick sex. The correlation of egg weight to posthatching chick weight decreases with increasing age of the chick. A 1 g change in egg weight has been shown to result in a corresponding change of 2–13 g in broiler weight at 6 to 8 weeks of age. This effect is much greater in eggs from young breeders than in those from old breeders. The effects of egg weight on chick feed conversion have been variable with no clear conclusion. Improved growth and uniformity may be obtained by growing chicks separately according to hatchling size. Therefore, sorting eggs by weight prior to incubation might be advantageous in some production operations to improve broiler or pullet uniformity and efficiency.