Congruence between breeding and wintering biodiversity hotspots: A case study in farmlands of Western Poland

Farmland landscapes are recognized as important ecosystems, not only for their rich biodiversity but equally so for the human beings who live and work in these places. However, biodiversity varies among sites (spatial change) and among seasons (temporal change). In this work, we tested the hypothesis that bird diversity hotspots distribution for breeding is congruent with bird diversity hotspots for wintering season, focusing also the representation of protected areas for the conservation of local hotspots. We proposed a framework based on the  use of species richness, functional diversity, and evolutionary distinctiveness to characterize avian communities. Although our findings show that the spatial distribution of local bird hotspots differed slightly between seasons, the protected areas’ representation was similar in both seasons. Protected areas covered 65% of the most important zones for breeding and 71% for the wintering season in the farmland studied. Functional diversity showed similar patterns as did bird species richness, but this measure can be most effective for highlighting differences on bird community composition. Evolutionary distinctiveness was less congruent with species richness and functional diversity, among seasons. Our findings suggest that inter-seasonal spatial congruence of local hotspots can be considered as suitable areas upon which to concentrate greater conservation efforts. However, even considering the relative congruence of avian diversity metrics at a local spatial scale, simultaneous analysis of protected areas while inter-seasonally considering hotspots, can provide a more complete representation of ecosystems for assessing the conservation status and designating priority areas

Hemi-field memory for attractiveness

In order to determine whether or not facial attractiveness plays a role in hemispheric facial memory, 35 right-handed participants first assigned attractiveness ratings to faces and then performed a recognition test on those faces in the left visual half-field (LVF) and right visual half-field (RVF). We found significant interactions between the experimental factors and visual half- field. There were significant differences in the extreme ends of the rating scale, that is, the very unattractive versus the very attractive faces: Female participants remembered very attractive faces of both women and men, with memory being superior in the RVF than in the LVF. In contrast, the male participants remembered very unattractive faces of both women and men; RVF memory was better than the LVF for women faces while for men faces memory was superior in the LVF. The interactions with visual half-field suggest that hemispheric biases in remembering faces are influenced by degree of attractiveness

Global divergence of microbial genome sequences mediated by propagating fronts

We model the competition between recombination and point mutation in microbial genomes, and present evidence for two distinct phases, one uniform, the other genetically diverse. Depending on the specifics of homologous recombination, we find that global sequence divergence can be mediated by fronts propagating along the genome, whose characteristic signature on genome structure is elucidated, and apparently observed in closely-related {\it Bacillus} strains. Front propagation provides an emergent, generic mechanism for microbial "speciation", and suggests a classification of microorganisms on the basis of their propensity to support propagating fronts

Hedging our bets: the expected contribution of species to future phylogenetic diversity

If predictions for species extinctions hold, then the `tree of life' today may be quite different to that in (say) 100 years. We describe a technique to quantify how much each species is likely to contribute to future biodiversity, as measured by its expected contribution to phylogenetic diversity. Our approach considers all possible scenarios for the set of species that will be extant at some future time, and weights them according to their likelihood under an independent (but not identical) distribution on species extinctions. Although the number of extinction scenarios can typically be very large, we show that there is a simple algorithm that will quickly compute this index. The method is implemented and applied to the prosimian primates as a test case, and the associated species ranking is compared to a related measure (the `Shapley index'). We describe indices for rooted and unrooted trees, and a modification that also includes the focal taxon's probability of extinction, making it directly comparable to some new conservation metrics.Comment: 19 pages, 2 figure

Computing evolutionary distinctiveness indices in large scale analysis

Abstract We present optimal linear time algorithms for computing the Shapley values and 'heightened evolutionary distinctiveness' (HED) scores for the set of taxa in a phylogenetic tree. We demonstrate the efficiency of these new algorithms by applying them to a set of 10,000 reasonable 5139-species mammal trees. This is the first time these indices have been computed on such a large taxon and we contrast our finding with an ad-hoc index for mammals, fair proportion (FP), used by the Zoological Society of London's EDGE programme. Our empirical results follow expectations. In particular, the Shapley values are very strongly correlated with the FP scores, but provide a higher weight to the few monotremes that comprise the sister to all other mammals. We also find that the HED score, which measures a species' unique contribution to future subsets as function of the probability that close relatives will go extinct, is very sensitive to the estimated probabilities. When they are low, HED scores are less than FP scores, and approach the simple measure of a species' age. Deviations (like the Solendon genus of the West Indies) occur when sister species are both at high risk of extinction and their clade roots deep in the tree. Conversely, when endangered species have higher probabilities of being lost, HED scores can be greater than FP scores and species like the African elephant Loxondonta africana, the two solendons and the thumbless bat Furipterus horrens can move up the rankings. We suggest that conservation attention be applied to such species that carry genetic responsibility for imperiled close relatives. We also briefly discuss extensions of Shapley values and HED scores that are possible with the algorithms presented here.</jats:p

Cognitive consequences of perceiving social exclusion

Although a great deal is now known about how people mentally represent individuals and groups, less attention has been paid to the question of how interpersonal relationships are represented in memory. Drawing on principles of categorization, this paper reports an investigation into how we mentally represent the relationships of others. In three experiments, evidence for assimilation effects following social exclusion (and subsequent categorization) is found. Experiment 1 uses a judgment paradigm to demonstrate that social exclusion influences the perception of interpersonal closeness. Experiments 2 and 3 employ a memory confusion paradigm to establish that representations of relationship partners are assimilated following the exclusion of a third party. © 2008 Elsevier Inc. All rights reserved

Do partnered women discriminate men's faces less along the attractiveness dimension?

Romantic relationships can have positive effects on health and reproductive fitness. Given that attractive potential alternative mates can pose a threat to romantic relationships, some researchers have proposed that partnered individuals discriminate opposite-sex individuals less along the physical attractiveness dimension than do unpartnered individuals. This effect is proposed to devalue attractive (i.e., high quality) alternative mates and help maintain romantic relationships. Here we investigated this issue by comparing the effects of men's attractiveness on partnered and unpartnered women's performance on two response measures for which attractiveness is known to be important: memory for face photographs (Study 1) and the reward value of faces (Study 2). Consistent with previous research, women's memory was poorer for face photographs of more attractive men (Study 1) and more attractive men's faces were more rewarding (Study 2). However, in neither study were these effects of attractiveness modulated by women's partnership status or partnered women's reported commitment to or happiness with their romantic relationship. These results do not support the proposal that partnered women discriminate potential alternative mates along the physical attractiveness dimension less than do unpartnered women