Intransitivity and coexistence in four species cyclic games

Intransitivity is a property of connected, oriented graphs representing species interactions that may drive their coexistence even in the presence of competition, the standard example being the three species Rock-Paper-Scissors game. We consider here a generalization with four species, the minimum number of species allowing other interactions beyond the single loop (one predator, one prey). We show that, contrary to the mean field prediction, on a square lattice the model presents a transition, as the parameter setting the rate at which one species invades another changes, from a coexistence to a state in which one species gets extinct. Such a dependence on the invasion rates shows that the interaction graph structure alone is not enough to predict the outcome of such models. In addition, different invasion rates permit to tune the level of transitiveness, indicating that for the coexistence of all species to persist, there must be a minimum amount of intransitivity.Comment: Final, published versio

Integrating ecosystem services into conservation strategies for freshwater and marine habitats: a review

Over the last two decades, there has been increasing public and political recognition of society's dependency upon natural habitat complexity and ecological processes to sustain provision of crucial ecosystem services, ranging from supplying potable water through to climate regulation. How has the ecosystem-services perspective been integrated into strategies for aquatic habitat conservation? Literature on conservation of diverse freshwater and marine habitats was reviewed to assess the extent to which past and current strategies specifically targeted ecosystem services, and considered ecosystem functions, potential trade-offs and social issues when formulating protection measures for conserving aquatic habitats. Surprisingly few published examples exist where comprehensive assessment of ecosystem services supported development of conservation plans. Seldom were aquatic habitat conservation objectives framed in terms of balancing trade-offs, assessing social values and evaluating suites of ecosystem services under different strategies. Time frames for achieving these objectives were also rarely specified. There was no evidence for fundamental differences between marine and freshwater habitats with respect to their ecosystem services that should be considered when setting targets for their conservation. When an ecosystem-service perspective is used for setting objectives in aquatic habitat conservation, the following actions are recommended: (1) explicitly listing and evaluating full suites of ecosystem services to be conserved; (2) identifying current and future potential trade-offs arising from conservation; (3) specifying time frames within which particular strategies might protect or enhance desired services; and (4) predicting how different proposed strategies might affect each ecosystem function, service flow and public benefit. This approach will help ensure that less-apparent ecosystem services (e.g. regulating, supporting) and their associated ecosystem functions receive adequate recognition and protection in aquatic conservation of freshwater and marine habitats. However, conservation objectives should not focus solely on protecting or enhancing ecosystem services but complement current strategies targeting biodiversity and other conservation goals.Peer Reviewe

Social relationships in a group of horses without a mature stallion

1. The social relationships in a group of Icelandic horses without a mature stallion were studied. The horses were all familiar to each other. Mutual grooming and play relationships, spatial associations, dominance-subordinate relations and the effect of kinship on these relationships were analysed. 2. The social structure was clearly dominated by the behaviour of the adult mares. The horses preferred to form bonds within their social class (sex/age) and they kept close proximity with their friends. The group was effectively divided into two social subgroups, adult mares as one group and adult geldings and sub-adults as another group. The sub-adults and adult geldings formed associations, which were based on mutual grooming and play, while the adult mares did not play. Differences between the sexes were evident. Males played more than the females, had more playing partners and were more popular as playmates. 3. Aggression rates were low. The dominance hierarchy was linear. Adult mares ranked higher than adult geldings, sub-adults and the foals. Rank was significantly correlated with age. The closer the adult mares were in rank, the more they groomed with each other. Such relationships were not found amongst the other social group. 4. Kinship was calculated between all pairs of animals for up to 4 or 5 generations. Allogrooming and play frequencies and proximity were all positively correlated with kinship. Adult mares, which were close in the dominance hierarchy, were on average more related than those further apart. 5. The social relationships in the Icelandic herd were, to some extent, different from relationships reported from unmanaged and feral horse-herds with mature stallions and bachelors. Our results suggest that adult mares groom more in groups without a stallion. Furthermore, they have more preferred partners than in natural harems and their partners are other adult mares, not their weaned offspring as seems to be the case in feral herds. The sub-adults also seem to be more socially active in the absence of stallions. Interestingly, in the Icelandic group, the adult mares showed stallion like behaviours, like mounting and protecting foals. Only by studying the behaviour and the nature of the relationships of horses in groups of different compositions, can we expect to gain a comprehensive understanding about individual social strategies and cognitive capabilities of the species. Such knowledge is valuable for management and welfare of the horse

Decades of Recovery From Sheep Grazing Reveal No Effects on Plant Diversity Patterns Within Icelandic Tundra Landscapes

Tundra plant communities are often shaped by topography. Contrasting wind exposure, slopes of different inclination and landforms of different curvature affect habitat conditions and shape plant diversity patterns. The majority of tundra is also grazed by ungulates, which may alter topographically induced plant diversity patterns, but such effects may depend on the spatial scales of assessments. Here we ask whether topographically induced patterns of within (alpha) and between (beta) plant community diversity are different in contrasting grazing regimes. We studied plant communities within tundra landscapes that were located in the North and Northwest of Iceland. Half of the studied landscapes were grazed by sheep, whereas the other half was currently un-grazed and recovering for several decades (up to 60 years). Alpha and beta diversity were assessed on explicitly defined, nested spatial scales, which were determined by topographical units. Although we contrasted currently grazed vegetation to vegetation that witnessed several decades of grazing recovery, we found no statistically significant differences in plant diversity patterns. We relate these findings to the low resilience of our study system toward grazing disturbances, which has important implications for management practices in the tundra. Effects of topography on species richness were only found for specific spatial scales of analyses. Species rich topographical units were associated with relatively large biomass of plant growth forms that promote nutrient availability and potential plant productivity in the tundra, such as forbs. This suggests that biomass of such plant growth forms within habitats can be a useful proxy of potential plant productivity and may predict spatial patterns of plant species richness in tundra

75% success rate after open debridement, exchange of tibial insert, and antibiotics in knee prosthetic joint infections.

Background and purpose - Prosthetic joint infection (PJI) is a leading cause of early revision after total knee arthroplasty (TKA). Open debridement with exchange of tibial insert allows treatment of infection with retention of fixed components. We investigated the success rate of this procedure in the treatment of knee PJIs in a nationwide material, and determined whether the results were affected by microbiology, antibiotic treatment, or timing of debridement. Patients and methods - 145 primary TKAs revised for the first time, due to infection, with debridement and exchange of the tibial insert were identified in the Swedish Knee Arthroplasty Register (SKAR). Staphylococcus aureus was the most common pathogen (37%) followed by coagulase-negative staphylococci (CNS) (23%). Failure was defined as death before the end of antibiotic treatment, revision of major components due to infection, life-long antibiotic treatment, or chronic infection. Results - The overall healing rate was 75%. The type of infecting pathogen did not statistically significantly affect outcome. Staphylococcal infections treated without a combination of antibiotics including rifampin had a higher failure rate than those treated with rifampin (RR = 4, 95% CI: 2-10). In the 16 cases with more than 3 weeks of symptoms before treatment, the healing rate was 62%, as compared to 77% in the other cases (p = 0.2). The few patients with a revision model of prosthesis at primary operation had a high failure rate (5 of 8). Interpretation - Good results can be achieved by open debridement with exchange of tibial insert. It is important to use an antibiotic combination including rifampin in staphylococcal infections