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Mammals are exposed to a diverse array of parasites and infectious diseases, many of which affect host survival and reproduction. Species that live in dense populations, large social groups, or with promiscuous mating systems may be especially vulnerable to infectious diseases owing to the close proximity and higher contact rates among individuals. We review the effects of host density and social contacts on parasite spread and the importance of promiscuity and mating structure for the spread and evolution of sexually transmitted diseases. Host social organization and mating system should influence not only parasite diversity and prevalence but may also determine the fitness advantages of different transmission strategies to parasites.

JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact support@jstor.org. Summary1 In laboratory microcosm experiments, co-occurring plant species were found to support very different rates of sporulation of arbuscular mycorrhizal (AM) fungi. These differences were not affected by the time of harvest, suggesting that they reflect host-dependent differences in fungal growth rates, rather than host-dependent timing of sporulation. 2 Spore counts in field soil and estimates from sorghum trap cultures showed that the association of AM fungi with particular host plants in the field was positively correlated with the sporulation rates observed on those hosts in the microcosm experiments. 3 The AM fungal species richness observed at the field site was high relative to estimates made in previous studies. 23 distinct species of AM fungi were found, seven of which have not been previously described. 4 The host-dependence of the relative growth rates of fungal populations may play an important role in the maintenance of fungal species diversity.

Sexually transmitted diseases (STDs) have been generally thought of as a small subset of infectious diseases, rather than as an important group of diseases that occur in numerous species. In this paper, we have (1) briefly reviewed theoretical studies on the dynamics of STDs; (2) documented the distribution of STDs in the animal kingdom; and (3) investigated whether STDs have characteristics which distinguish them from other infectious diseases. The dynamics of STDs should differ from those of ordinary infectious diseases because their transmission depends on the frequency rather than density of infectives. With this type of transmission, there is no threshold density for disease spread, and the conditions for host-pathogen coexistence are more restrictive. Nevertheless, a wide variety of disease characteristics may allow a sexually transmitted pathogen to coexist with its host. We found over 200 diseases for which there was evidence of sexual transmission. They occurred in groups as diverse as mammals, reptiles, arachnids, insects, molluscs and nematodes. Sexually transmitted pathogens included protozoans, fungi, nematodes, helminths, and cancerous cell lines, as well as bacteria and viruses. Detailed comparison of the characteristics of sexually transmitted mammalian diseases with those that are transmitted by non-sexual means, showed that STDs cause less mortality, are longer-lived in their hosts, are less likely to invoke strong immune responses, have narrower host-ranges, and show less fluctuation in prevalence over time. These shared features are related to mode of transmission rather than either host or pathogen taxonomic affiliation. This suggests an evolutionary explanation based on shared ecologies rather than one based on phylogenetic history.

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Insufficient genetic variability and the swamping effects of gene flow are inadequate explanations of limits to natural selection. Comparison of evolutionary responses in different populations subjected to similar selective forces, comparison of rare and widespread species, and comparison of marginal and central populations are all neglected research areas that bear on the nature of limits to natural selection. Plant populations provide us with well-defined, operationally viable systems for addressing these comparisons. Several possible constraints on range extension of ecologically marginal populations are considered in detail. Selection on fitness components that are themselves negatively correlated will be ineffective: such negative correlations are to be expected in natural populations. Small size of marginal populations will reduce severely the probability of obtaining appropriate character combinations; it will increase the swamping effects of gene flow; and it may lead to inbreeding depression effects. Gene flow will have different effects depending on whether the genes concerned are effectively neutral, advantageous, or deleterious in the population into which they migrate. Gene flow will spread beneficial genes rapidly, but may retard divergence if density of marginal populations is low and swamping effects are high. Finally a population entering a new habitat is likely to meet new competitors and predators: the revolutionary responses of the latter may counteract adaptive responses by the species undergoing range extension. All these factors are likely to interact in important ways in marginal populations. The study of limits to natural selection is likely to be a fruitful future research area, and one in which the detailed documentation of the systematist will provide invaluable baseline information.

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Pathogens that infect multiple hosts are commonly transmitted by vectors, and their transmission rate is often thought to depend on the proportion of hosts or vectors infected (i.e., frequency dependence). A model of a two-host, one-pathogen system with frequency-dependent transmission is used to investigate how sharing a pathogen with an alternative host influences pathogen-mediated extinction. The results show that if there is frequency-dependent transmission, a host can be rescued from pathogen-mediated extinction by the presence of a second host with which it shares a pathogen. The study provides an important conceptual counterexample to the idea that shared pathogens necessarily result in apparent competition by showing that shared pathogens can mediate apparent mutualism. We distinguish two types of dilution effect (pathogen reduction with increasing host diversity), each resulting from different underlying pathogen transmission processes and host density effects. These results have important consequences for understanding the role of pathogens in species interactions and in maintaining host species diversity.