Chapter 1: Assessing a planet in transformation: Rationale and approach of the IPBES Global Assessment on Biodiversity and Ecosystem Services

The challenges of mitigating and adapting to climate change, achieving inclusive food, water, energy and health security, addressing urban vulnerabilities, and the unequal burdens of nature deterioration, are not only predicaments on their own right. Because they interact, often exacerbating each other, they create new risks and uncertainties for people and nature. It is now evident that the rapid deterioration of nature, including that of the global environmental commons on land, ocean, atmosphere and biosphere, upon which humanity as a whole depends, are interconnected and their cascading effects compromise societal goals and aspirations from local to global levels. Growing efforts to respond to these challenges and awareness of our dependence on nature have opened new opportunities for action and collaboration towards fairer and more sustainable futures.The global assessment on biodiversity and ecosystem services (GA) has been designed to be a comprehensive and ambitious intergovernmental integrated assessment of recent anthropogenic transformations of Earth?s living systems, the roots of such transformations, and their implications to society. In the chapters that follow, our mandate is to critically assess the state of knowledge on recent past (from the 1970s), present and possible future trends in multi-scale interactions between people and nature, taking into consideration different worldviews and knowledge systems, including those representing mainstream natural and social sciences and the humanities, and indigenous and local knowledge systems. In doing so, the GA also assesses where the world stands in relation to several international agreements related to biodiversity and sustainable development.Fil: Brondizio, Eduardo. No especifíca;Fil: Díaz, Sandra Myrna. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; ArgentinaFil: Settele, Josef. No especifíca;Fil: Ngo, Hien. No especifíca;Fil: Guèze, Maximilien. No especifíca;Fil: Aumeeruddy-Thomas, Y. No especifíca;Fil: Bai, Xuemei. No especifíca;Fil: Geschke, Arne. No especifíca;Fil: Molnár, Zsolt. No especifíca;Fil: Niamir, Aidin. No especifíca;Fil: Pascual, Unai. No especifíca;Fil: Simcock, Alan. No especifíca;Fil: Jaureguiberry, Pedro. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto Multidisciplinario de Biología Vegetal. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas Físicas y Naturales. Instituto Multidisciplinario de Biología Vegetal; ArgentinaFil: Hien, Ngo,. No especifíca;Fil: Brancalion, Pedro. No especifíca;Fil: Chan, Kai M. A.. No especifíca;Fil: Dubertret, Fabrice. No especifíca;Fil: Hendry, Andrew. No especifíca;Fil: Liu, Jianguo. No especifíca;Fil: Martin, Adrian. No especifíca;Fil: Martín López, Berta. No especifíca;Fil: Midgley, Guy F.. No especifíca;Fil: Obura, David. No especifíca;Fil: Oliver, Tom. No especifíca;Fil: Scheffran, Jürgen. No especifíca;Fil: Seppelt, Ralf. No especifíca;Fil: Strassburg, Bernardo. No especifíca;Fil: Spangenberg, Joachim H.. No especifíca;Fil: Stenseke, Marie. No especifíca;Fil: Turnhout, Esther. No especifíca;Fil: Williams, Meryl J.. No especifíca;Fil: Zayas, Cynthia. No especifíca

Lack of Respiratory Chain Complex I Impairs Alternative Oxidase Engagement and Modulates Redox Signaling during Elicitor-Induced Cell Death in Tobacco

Alternative oxidase (AOX) functions in stress resistance by preventing accumulation of reactive oxygen species (ROS), but little is known about in vivo partitioning of electron flow between AOX and the cytochrome pathway. We investigated the relationships between AOX expression and in vivo activity in Nicotiana sylvestris and the complex I–deficient CMSII mutant in response to a cell death elicitor. While a specific AOX1 isoform in the active reduced state was constitutively overexpressed in CMSII, partitioning through the alternative pathway was similar to the wild type. Lack of correlation between AOX content and activity indicates severe metabolic constraints in nonstressed mutant leaves. The bacterial elicitor harpin N(Ea) induced similar timing and extent of cell death and a twofold respiratory burst in both genotypes with little change in AOX amounts. However, partitioning to AOX was increased twofold in the wild type but remained unchanged in CMSII. Oxidative phosphorylation modeling indicated a twofold ATP increase in both genotypes. By contrast, mitochondrial superoxide dismutase activity and reduced forms of ascorbate and glutathione were higher in CMSII than in the wild type. These results demonstrate genetically programmed flexibility of plant respiratory routes and antioxidants in response to elicitors and suggest that sustained ATP production, rather than AOX activity by itself or mitochondrial ROS, might be important for in planta cell death

Comparative study of stress and quality of life in outpatients consulting for different dermatoses in 5 academic departments of dermatology.

International audienceIn this study, perceived stress and quality of life were measured with PCV-Metra and SF-12 scales in outpatients consulting for different dermatoses in 5 academic dermatology departments for 5 consecutive days. 658 patients were enrolled in the study. Perceived stress was higher in women and the mental component of their quality of life was more altered. Perceived stress was higher in Paris than in other areas and was respectively 11.4, 10.4, 9.2 and 8.9 for psoriasis, acne, atopic dermatitis and pigmented tumours. Perceived stress was correlated to mental quality of life. Stress was more elevated in people with inflammatory dermatoses than in those with tumours. To our knowledge, this is the first comparative study of both stress and quality of life levels in different dermatoses. Stress levels were lower in people with pigmented tumours, suggesting that they can be used as controls in comparative studies because they can be considered as healthy subjects. On the contrary, patients with psoriasis had a very high level of perceived stress and a deeply altered quality of life

Family-based association study of common variants, rare mutation study and epistatic interaction detection in HDAC genes in schizophrenia

International audienceBACKGROUND: Histone deacetylases (HDACs) are key enzymes of histone acetylation, and abnormalities in histone modifications and in the level of HDAC proteins have been reported in schizophrenia. The objective of the present study was to systematically test the HDAC genes for its association with schizophrenia. METHODS: A family-based genetic association study (951 Caucasian subjects in 313 nuclear families) using 601 tag-single nucleotide polymorphisms in HDAC genes was conducted followed by a replication study of top-ranked markers in a sample of 1427 Caucasian subjects from 241 multiplex families and 176 trios. Epistasis interaction was tested by using the pedigree-based generalized multifactor dimensionality reduction (GMDR). Furthermore, we analyzed exome sequencing data of 1134 subjects for detection of rare mutations in HDAC genomic regions. RESULTS: In the exploratory study, ten markers were in significant association with schizophrenia (P\textless0.01). One maker rs14251 (HDAC3) was replicated (P=0.04) and remained significant in the whole sample (P=0.004). GMDR identified that a significant three-locus interaction model was detected involving rs17265596 (HDAC9), rs7290710 (HDAC10) and rs7634112 (HDAC11) with a good testing accuracy (0.58). No rare mutations were found associated with schizophrenia. CONCLUSION: This first exploratory systematic study of the HDAC genes provides consistent support for the involvement of the HDAC3 gene in the etiology of schizophrenia. A statistical epistatic interaction between HDAC9, HDAC10, and HDAC11 was detected and seems biologically plausibl