Catálogo de publicaciones - revistas

<jats:p>Laanisto and Hutchings claim that the local species pool is a more important predictor of local plant species richness than biomass and that when the species pool is considered, there is no hump-backed relationship between biomass and richness. However, we show that by calculating a more appropriate measure of species pool, community completeness, both regional and local processes shape local richness.</jats:p>

<jats:p> Fraser <jats:italic>et al</jats:italic> . (Reports, 17 July 2015, p. 302) report that a hump-backed model describes the worldwide relationship between productivity and plant species richness in grassland communities. We reanalyze their data from a larger-scale perspective, using local species pool. This influences richness far more strongly than productivity, and, when this is taken into account, the hump-backed richness-productivity relationship disappears. </jats:p>

<jats:p>Cats and dogs are revealing some surprising insights into how animals age.</jats:p>

<jats:p>Pushing the limits of life span in animals could someday help lengthen our own.</jats:p>

<jats:p>In the race to find a biological clock, there are plenty of contenders.</jats:p>

<jats:p>Age is the greatest risk factor for nearly every major cause of mortality in developed nations. Despite this, most biomedical research focuses on individual disease processes without much consideration for the relationships between aging and disease. Recent discoveries in the field of geroscience, which aims to explain biological mechanisms of aging, have provided insights into molecular processes that underlie biological aging and, perhaps more importantly, potential interventions to delay aging and promote healthy longevity. Here we describe some of these advances, along with efforts to move geroscience from the bench to the clinic. We also propose that greater emphasis should be placed on research into basic aging processes, because interventions that slow aging will have a greater effect on quality of life compared with disease-specific approaches.</jats:p>

<jats:p>Telomeres are the protective end-complexes at the termini of eukaryotic chromosomes. Telomere attrition can lead to potentially maladaptive cellular changes, block cell division, and interfere with tissue replenishment. Recent advances in the understanding of human disease processes have clarified the roles of telomere biology, especially in diseases of human aging and in some aging-related processes. Greater overall telomere attrition predicts mortality and aging-related diseases in inherited telomere syndrome patients, and also in general human cohorts. However, genetically caused variations in telomere maintenance either raise or lower risks and progression of cancers, in a highly cancer type–specific fashion. Telomere maintenance is determined by genetic factors and is also cumulatively shaped by nongenetic influences throughout human life; both can interact. These and other recent findings highlight both causal and potentiating roles for telomere attrition in human diseases.</jats:p>

<jats:p>Research into stem cells and aging aims to understand how stem cells maintain tissue health, what mechanisms ultimately lead to decline in stem cell function with age, and how the regenerative capacity of somatic stem cells can be enhanced to promote healthy aging. Here, we explore the effects of aging on stem cells in different tissues. Recent research has focused on the ways that genetic mutations, epigenetic changes, and the extrinsic environmental milieu influence stem cell functionality over time. We describe each of these three factors, the ways in which they interact, and how these interactions decrease stem cell health over time. We are optimistic that a better understanding of these changes will uncover potential strategies to enhance stem cell function and increase tissue resiliency into old age.</jats:p>