Predation on primates: Ecological patterns and evolutionary consequences

It has long been thought that predation has had important ecological and evolutionary effects on primates as prey. Predation has been theorized to have been a major selective force in the evolution of hominids.¹ In modern primates, behaviors such as active defense, concealment, vigilance, flight, and alarm calls have been attributed to the selective pressures of predation, as has group living itself. It is clear that primates, like other animals, have evolved ways to minimize their risk of predation. However, the extent to which they have been able to do so, given other constraints of living such as their own need to acquire food, has not yet been resolved. Perhaps most hotly debated is whether predation has been the primary selective force favoring the evolution of group living in primates. Part of the difficulty in resolving the debate lies in a paucity of direct evidence of predation. This is regrettable yet understandable since primatologists, by definition, focus on the study of primates, not predators of primates (unless these are also primates). Systematic direct evidence of the effects of predation can best be obtained by studying predators that are as habituated to observers as are their primate prey. Until this is done, we must continue to rely on opportunistic accounts of predation and predation attempts, and on systematically obtained indirect evidence. Such data reveal several interesting patterns: (1) although smaller primates may have greater predation rates than larger primates, even the largest primates are not invulnerable to predation; (2) the use by primates of unfamiliar areas can result in higher predation rates, which might be one pressure favoring philopatry, or site fidelity; (3) arboreal primates are at greater risk of predation when they are more exposed (at forest edges and tops of canopies) than in more concealed locations; (4) predation by mammalian carnivores may often be episodic; and (5) terrestrial primates may not experience greater predation than arboreal primates.     

The role of introduced species in shaping the distribution and abundance of island reptiles

Summary Species interactions, as revealed by historical introductions of predators and competitors, affect population densities and sometimes result in extinctions of island reptiles. Mongoose introductions to Pacific islands have diminished the abundance of diurnal lizards and in some cases have led to extinctions. Through these population level effects, biogeographic patterns are produced, such as the reciprocal co-occurrence pattern seen with the tuatara and its predator, the Polynesian rat, and with the tropical gecko competitorsHemidactylus frenatus andLepidodactylus lugubris in urban habitats in the Pacific. Although competition has led to changes in abundance and has caused habitat displacement and reduced colonization success, extinctions of established reptile populations usually occur only as a result of predation.These introductions, along with many manipulative experiments, demonstrate that present day competition and predation are potent forces shaping community structure and geographic distributions. The human introduction of species to islands can be viewed as an acceleration of the natural processes of range expansion and colonization. The immediate biotic consequences of these natural processes should be of the same intensity as those of the human introductions. Coevolution may subsequently act to ameliorate these interactions and reduce the dynamical response of one species to the other. The role played by coevolution in mediating interactions between competitors and predator and prey is highlighted by the susceptibility of predator-naive endemic species to introduced predators and the invalidity of species-poor communities.     

Food limitation of planktonic rotifers: field experiments in two mountain ponds

1. Resource competition is thought to be important in controlling zooplankton population dynamics and structuring zooplankton communities. Resource competition requires that resources are limiting. Ten field experiments were conducted to determine the presence and intensity of resource limitation of herbivorous planktonic rotifers in two mountain ponds. The intensity of food limitation was measured as Δ r , the difference between population growth rates in food supplemented versus control enclosures.
2. Rotifers were significantly food limited (Δ r  > 0) in most experiments. The intensity of food limitation varied between species. In Grady Lake, mean Δ r was 0.26 day⁻¹ for Polyarthra vulgaris and 0.43 day⁻¹ for an unidentified Synchaeta sp. In L1 Pond, mean Δ r was 0.07 day⁻¹ for Keratella cochlearis and 0.28 day⁻¹ for S. oblonga . The frequent and intense food limitation suggests that edible phytoplankton in both ponds were often present at low densities, were of low nutritional quality, or both. The intensity of food limitation often changed rapidly over time, indicating rapid temporal variation in resource availability.
3. For P. vulgaris , Δ r was not correlated with its population growth rate in Grady Lake. Thus, although food limitation was common, population dynamics may have been more strongly affected by other factors. For K. cochlearis , Δ r increased as population density increased, suggesting the existence of intraspecific resource competition that may regulate population dynamics.     

Rodent seed predation promotes differential recruitment among bird-dispersed trees in temperate secondary forests

We investigated the role of seed predation by rodents in the recruitment of the fleshy-fruited trees Taxus baccata, Ilex aquifolium and Crataegus monogyna in temperate secondary forests in NW Spain. We measured the densities of dispersed seeds, early emerged seedlings, established recruits and adults, at four sites over a period of 2 years. Seed predation among species was compared by seed removal experiments and analysis of rodent larder-hoards. The three species differed markedly in local regeneration patterns. The rank order in the seed rain following decreasing seed density was Ilex, Taxus and Crataegus. However, Crataegus established 3.3 times more seedlings than Taxus. For all species, there was a positive linear relationship between the density of emerged seedlings and seed density, suggesting that recruitment was seed- rather than microsite-limited. A consistent pattern of seed selection among species was exerted by rodents, which preferred Taxus and, secondarily, Ilex seeds to Crataegus seeds. Predation ranking was the inverse of that of seed protection against predators, measured as the mass of woody coat per mass unit of the edible fraction. Recruitment potential, evaluated as the ratio of seedlings to seeds, was negatively related to seed predation, with the rank order Crataegus > Ilex > Taxus. The selective early recruitment limitation exerted by predation may have a demographic effect in the long term, as judged by the positive relationship between early seedling emergence and the density of established recruits. By modulating the pre-emptive competition for seed safe sites, rodents may preclude the progressive exclusion of species that produce low numbers of seeds (i.e. Crataegus) by those dominant in seed number (i.e. Ilex, Taxus), or at least foster the evenness for site occupation among seedlings of different species.     

Infertile seeds ofYucca schottii: A beneficial role for the plant in the yucca-yucca moth mutualism?

Summary The yucca-yucca moth interaction is a classic case of obligate mutualism. Female moths pollinate and oviposit in the gynoecium of the flower; however, maturing larvae eat a fraction of the developing seeds. We studied within-fruit distributions of four seed types (fertile, infertile, eaten and uneaten seeds) in order to evaluate costs and benefits in aYucca schottii population in southeastern Arizona. We focused on how the spatial arrangement of seeds affected larval behaviour and, hence, the costs of the mutualism to the yucca. Infertile seeds were distributed throughout both infested and uninfested locules. Additionally, moth larvae feeding in a single locule preferred fertile seeds and even avoided infertile seeds and left the fruit significantly more often when they encountered infertile seeds. We suggest that, regardless of the cause of infertile seeds, they function as blocking units within seed locules and therefore reduce seed predation by moth larvae. We also suggest that, together with certain other fruit traits, the presence of infertile seeds promotes the evolutionary stability of this pollination mutualism.     

The dynamics of acute malaria infections. I. Effect of the parasite's red blood cell preference

What determines the dynamics of parasite and anaemia during acute primary malaria infections? Why do some strains of malaria reach higher densities and cause greater anaemia than others? The conventional view is that the fastest replicating parasites reach the highest densities and cause the greatest loss of red blood cells (RBCs). Other current hypotheses suggest that the maximum parasite density is achieved by strains that either elicit the weakest immune responses or infect the youngest RBCs (reticulocytes). Yet another hypothesis is a simple resource limitation model where the peak parasite density and the maximum anaemia (percentage loss of RBCs) during the acute phase of infection equal the fraction of RBCs that the malaria parasite can infect. We discriminate between these hypotheses by developing a mathematical model of acute malaria infections and confronting it with experimental data from the rodent malaria parasite Plasmodium chabaudi. We show that the resource limitation model can explain the initial dynamics of infection of mice with different strains of this parasite. We further test the model by showing that without modification it closely reproduces the dynamics of competing strains in mixed infections of mice with these strains of P. chabaudi. Our results suggest that a simple resource limitation is capable of capturing the basic features of the dynamics of both parasite and RBC loss during acute malaria infections of mice with P. chabaudi, suggesting that it might be worth exploring if similar results might hold for other acute malaria infections, including those of humans.     

The fast life of a dwarfed giant

In the first half of the 1960s, a rich paleontological site was discovered at Spinagallo caves (Eastern Sicily, Southern Italy). A very abundant fossil population (at least 104 specimens) of the dwarf elephant Elephas falconeri, the smallest elephant that ever lived, was recovered. We computed the survivorship curve for this fossil population in order to investigate both the great juvenile abundance and high calf mortality which it shows. Through the analysis of E. falconeri survivorship, of some reconstructed life-history traits, and of its ecology, and taking into account the Island rule (Foster, 1964), we concluded that E. falconeri moved somewhat toward the fast extreme of the slow-fast continuum in life-history traits in regards to its mainland ancestor E. antiquus, that is, it was somehow r-selected. In keeping with our findings, we propose a new explanation for the common occurrence of dwarfism in large mammals living on islands. We suggest the interplay of competition, resource allocation shift and feeding niche width could successfully explain this pattern.     

Thermal adaptation affects interactions between a range‐expanding and a native odonate species

1. Increasing temperature and invading species may interact in their effects on communities. In this study, we investigated how rising temperatures alter larval interactions between a naturally range‐expanding dragonfly, Crocothemis erythraea, and a native northern European species, Leucorrhinia dubia. Initial studies revealed that C. erythraea grow up to 3.5 times faster than L. dubia at temperatures above 16 °C. As a result, we hypothesised that divergent temperature responses would lead to rapid size differences between coexisting larvae and, consequently, to asymmetric intraguild predation at higher ambient temperatures. 2. Mortality and growth rates were measured in interaction treatments (with both species present) and non‐interaction controls (one species present) at four different temperature regimes: at an ambient temperature representative of central Germany, where both species overlap in distribution, and at temperatures increased by 2, 4 and 6 °C. 3. The mortality of C. erythraea did not differ between treatment and control. In contrast, mortality of L. dubia remained similar over all temperatures in the controls, but increased with temperature in the presence of the other species and was significantly higher there than in the controls. We concluded that L. dubia suffered asymmetric intraguild predation, particularly at increased temperature. Reduced growth rate of L. dubia in the interaction treatment at higher temperatures also suggested asymmetric competition for prey in the first phase of the experiment. 4. The results imply that the range expansion of C. erythraea may cause reduction in population size of syntopic L. dubia when temperature rises by more than 2 °C. The consequences for future range patterns, as well as other factors that may influence the interaction in nature, are discussed.