In this paper we derive from first principles the expected body sizes of the parasite communities that can coexist in a mammal of given body size. We use a mixture of mathematical models and known allometric relationships to examine whether host and parasite life histories constrain the diversity of parasite species that can coexist in the population of any host species. The model consists of one differential equation for each parasite species and a single density-dependent nonlinear equation for the affected host under the assumption of exploitation competition. We derive threshold conditions for the coexistence and competitive exclusion of parasite species using invasion criteria and stability analysis of the resulting equilibria. These results are then used to evaluate the range of parasites species that can invade and establish in a target host and identify the ‘optimal’ size of a parasite species for a host of a given body size; ‘optimal’ is defined as the body size of a parasite species that cannot be outcompeted by any other parasite species. The expected distributions of parasites body sizes in hosts of different sizes are then compared with those observed in empirical studies. Our analysis predicts the relative abundance of parasites of different size that establish in the host and suggests that increasing the ratio of parasite body size to host body size above a minimum threshold increases the persistence of the parasite population.

A major issue for the proper understanding of the evolution of life-cycle histories is the regulation of voltinism and its variation. Diapause characteristics are known to regulate voltinism, but the underlying mechanisms are poorly understood. This paper studies diapause duration and voltinism variation in a haematophagous diptera parasitizing 2 sympatric hosts with very different breeding phenologies. We hypothesize that bivoltinism will be more frequent in carnid flies parasitizing an early breeding, multi-brooded species than in flies parasitizing a late breeder, single-brooded species. We obtained evidence of the co-occurrence of uni- and bivoltinism in both clutches of the multi-brooded Spotless starling (Sturnus unicolor) as well as in clutches of the single-brooded European roller (Coracias garrulus). Unexpectedly, the proportion of bivoltine flies was similar in both host species. A remarkable degree of host-parasite synchronization at the population level was found for bivoltine flies. Our findings reveal the facultative nature of diapause in Carnus. We discuss the influence of abiotic conditions and host availability on polymorphism in life-history cycles and the consequences both for the parasite and the host.

Avian hosts may either resist the negative effects of nestling ectoparasites by minimizing the number of parasites, or tolerate parasitism by increasing their fecundity via the reproductive compensation hypothesis. Little is known about the interactions between ectoparasites and their avian hosts in the tropics. We (1) examined nestling development rates, and tested whether (2) parasitism by a subcutaneous ectoparasitic botfly (Philornis sp.) had negative effects on the condition of nestlings, and (3) these negative effects were minimized in larger broods in a tropical cavity-nesting bird, the planalto woodcreeper (Dendrocolaptes platyrostris), in primary and secondary Atlantic forests in the northern province of Misiones, Argentina. Nestling mass and ectoparasite load per nestling reached maxima when nestlings (n = 50) were between 10 and 14 d old. General linear mixed models predicted that mass at fledging declined with increasing nestling parasite load, suggesting that botflies had a negative influence on fledging condition. Parasite load per nestling declined with increasing brood size indicating that woodcreepers that increase their reproductive output minimize the negative effects of parasitism. Overall we found evidence to support the tolerance via reproductive compensation hypothesis. Future tests of the reproductive compensation hypothesis may help determine the underlying mechanism of the observed negative correlation between parasite load of nestlings and brood size.

Parasites with complex life cycles have developed numerous and very diverse adaptations to increase the likelihood of completing this cycle. For example, some parasites can abbreviate their life cycles by skipping the definitive host and reproducing inside their intermediate host. The resulting shorter life cycle is clearly advantageous when definitive hosts are absent or rare. In species where life-cycle abbreviation is facultative, this strategy should be adopted in response to seasonally variable environmental conditions. The hermaphroditic trematode Coitocaecum parvum is able to mature precociously (progenesis), and produce eggs by selfing while still inside its amphipod second intermediate host. Several environmental factors such as fish definitive host density and water temperature are known to influence the life-history strategy adopted by laboratory raised C. parvum. Here we document the seasonal variation of environmental parameters and its association with the proportion of progenetic individuals in a parasite population in its natural environment. We found obvious seasonal patterns in both water temperature and C. parvum host densities. However, despite being temporally variable, the proportion of progenetic C. parvum individuals was not correlated with any single parameter. The results show that C. parvum life-history strategy is not as flexible as previously thought. It is possible that the parasite's natural environment contains so many layers of heterogeneity that C. parvum does not possess the ability to adjust its life-history strategy to accurately match the current conditions.

Adult female survival as a potential proximate factor responsible for observed changes in southern elephant seal Mirounga leonina populations was investigated. We compared the survival rate estimates from mark–recapture data for female elephant seals from the Marion Island population (using program MARK) for two periods (pre- and post-decline) during the past 15 years and with estimates from another population in southern Argentina, which had increased steadily during the same period. Survival of prime-age adult females increased significantly by 6.2% during the latter part of the decline at Marion Island, and the survival of adult females at the colony in southern Argentina was 3.2% greater than at Marion Island after the stabilization. We thereby demonstrated the importance of adult female survival in population regulation and emphasized the importance of monitoring adult females in order to understand population changes in southern elephant seals. In addition, we investigated whether reproductive expenditure early on in life reduces future reproductive potential in the population at Marion Island. We did this by estimating and comparing future survival and breeding probabilities of females primiparous at different ages. The future annual survival and breeding probabilities of females breeding at a young age, was similar to those from females primiparous at an older age. There was also no reduced survival in the year following first breeding in young or older first time breeders. Reproductive expenditure in young primiparous females therefore did not entail future fitness costs relative to older primiparous females, and we found no evidence supporting the existence of various life-history strategies in terms of age of primiparity within a population of southern elephant seals.

Four structural types of cerrado vegetation were examined to test the following hypotheses: (1) there are predictable changes in woody plant density, species richness and life-history strategies from one structural type to another; and (2) plant species composition in the less-rich structural types represent particular and impoverished subsets of those found in the richer ones. The study was conducted at Fazenda Palmares (5°33′S, 42°37′W) Piauí State, Brazil. A 47% decrease in woody plant density between cerradão (forest) and the least-dense type of cerrado sensu stricto (scrub) was associated with a 40% decrease in species richness. The percentage of lower-layer species was reduced by 29% in the least dense type of cerrado sensu stricto compared to cerradão. The proportion of species that flower and fruit during the rainy season was also reduced by one third. Species were not distributed as impoverished subsets along the cerradão–cerrado sensu stricto gradient. It is argued that the reduction in woody plant density and richness is partly due to factors limiting the occurrence of species with particular life-history strategies. The species composition of structural types is affected by the ‘mass effect’ and also by surrounding biotas, which provide species that colonize particular types of cerrado vegetation. Both these processes reduce the likelihood that the species composition in the poorer structural types are simple subsets of those present in the richer types.

Les deux espèces de sardinelles (Surdinella aurita et Sardinella maderensis) sont présentes dans les trois régions d'upwelling de l'Ouest africain (zones sénégalo-mauritanienne, ivoiro-ghanéenne et congoangolaise). La compétition entre ces deux espèces, présentant une grande similitude de forme, à l'activité et aux régimes alimentaires très proches et occupant les mêmes zones géographiques sembleeffective. Cependant les stratégies d'occupation et d'exploitation du milieu, de croissance et de reproduction sont, pour ces deux espèces, intimement liées à la dynamique des upwellings mais elles divergent en de nombreux points. Une complémentarité spatio-temporelle semble donc exister entre la dynamique de ces deux espèces dont les stratégies démographiques diffèrent. Sardinella aurita présente une plasticité et une adaptabilité remarquable aux fluctuations du milieu dont elle tire parti.En cela, elle semble être plus sensible aux variations climatiques que Sardinella maderensis, espèce tolérant de fortes perturbations de I'environnement. Sardinella aurita possède une stratégie adaptative plus souple liée à une grande plasticité démographique. Cela lui permet une meilleure utilisation d'unaccroissement d'enrichissement temporaire du milieu, mais en retour la population subit le contrecoup de façon plus drastique lorsque les conditions deviennent défavorables.

Même si la compétition entre deux espèces de poissons pélagiques peut souvent paraître effective en écologie marine, rares sont les exemples où elle peut être mise en évidence au niveau de l'abondance respective des stocks. Les mécanismes de la compétition pour des espèces spécialisées comme lespélagiques doivent être précisés au niveau de certains paramètres du cycle vital de l'espèce. L'analyse comparée des stratégies démographiques permet de mieux comprendre la nature différente de la dynamique des stocks, notamment l'organisation du partage de ressources communes. La nécessité de gérer les stocks en considérant la stratégie de vie des espèces qui les composent est soulignée.