31 research outputs found

    Eastern Pacific Warm Pool paleosalinity and climate variability : 0–30 kyr

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    Author Posting. © American Geophysical Union, 2006. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Paleoceanography 21 (2006): PA3008, doi:10.1029/2005PA001208.Multi-proxy geologic records of Ύ18O and Mg/Ca in fossil foraminifera from sediments under the Eastern Pacific Warm Pool (EPWP) region west of Central America document variations in upper ocean temperature, pycnocline strength, and salinity (i.e., net precipitation) over the past 30 ky. Although evident in the paleotemperature record, there is no glacial-interglacial difference in paleosalinity, suggesting that tropical hydrologic changes do not respond passively to high-latitude ice sheets and oceans. Millennial variations in paleosalinity with amplitudes as high as ~4 PSU occur with a dominant period of ~3-5 ky during the glacial/deglacial interval and ~1.0-1.5 ky during the Holocene. The amplitude of the EPWP paleosalinity changes greatly exceeds that of published Caribbean and western tropical Pacific paleosalinity records. EPWP paleosalinity changes correspond to millennial-scale climate changes in the surface and deep Atlantic and the high northern latitudes, with generally higher (lower) paleosalinity during cold (warm) events. In addition to Intertropical Convergence Zone (ITCZ) dynamics, which play an important role in tropical hydrologic variability, changes in Atlantic-Pacific moisture transport, which is closely linked to ITCZ dynamics, may also contribute to hydrologic variations in the EPWP. Calculations of interbasin salinity average and interbasin salinity contrast between the EPWP and the Caribbean help differentiate long-term changes in mean ITCZ position and Atlantic-Pacific moisture transport, respectively.Support for this research was provided by the U.S. National Science Foundation

    Genetic disruption of 21-hydroxylase in zebrafish causes interrenal hyperplasia

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    Congenital adrenal hyperplasia is a group of common inherited disorders leading to glucocorticoid deficiency. Most cases are caused by 21-hydroxylase deficiency (21OHD). The systemic consequences of imbalanced steroid hormone biosynthesis due to severe 21OHD remains poorly understood. Therefore, we have developed a zebrafish model for 21OHD, which focuses on the impairment of glucocorticoid biosynthesis. A single 21-hydroxylase gene (cyp21a2) is annotated in the zebrafish genome based on sequence homology. Our in silico analysis of the Cyp21a2 protein sequence suggests a sufficient degree of similarity for the usage of zebrafish cyp21a2 to model aspects of human 21OHD in vivo. We determined the spatio-temporal expression patterns of cyp21a2 by whole mount in situ hybridisation and RT-PCR throughout early development. Early cyp21a2 expression is restricted to the interrenal gland (zebrafish adrenal counterpart) and the brain. To further explore the in vivo consequences of 21-hydroxylase deficiency we created several cyp21a2 null-allele zebrafish lines employing a transcription activator-like effector nuclease genomic engineering strategy. Homozygous mutant zebrafish larvae showed an upregulation of the hypothalamic-pituitary-interrrenal axis and interrenal hyperplasia. Furthermore, Cyp21A2-deficient larvae had a typical steroid profile with reduced concentrations of cortisol and increased concentrations of 17-hydroxyprogesterone and 21-deoxycortisol. Affected larvae showed an upregulation of the hypothalamic-pituitary-interrrenal axis and interrenal hyperplasia. Downregulation of the glucocorticoid-responsive genes pck1 and fkbp5 indicated systemic glucocorticoid deficiency. Our work demonstrates the crucial role of Cyp21a2 in glucocorticoid biosynthesis in zebrafish larvae and establishes a novel in vivo model allowing for studies of systemic consequences of altered steroid hormone synthesis

    Carbon isotope discrimination of arctic and boreal biomes inferred from remote atmospheric measurements and a biosphere-atmosphere model

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    Estimating discrimination against ^(13)C during photosynthesis at landscape, regional, and biome scales is difficult because of large-scale variability in plant stress, vegetation composition, and photosynthetic pathway. Here we present estimates of ^(13)C discrimination for northern biomes based on a biosphere-atmosphere model and on National Oceanic and Atmospheric Administration Climate Monitoring and Diagnostics Laboratory and Institute of Arctic and Alpine Research remote flask measurements. With our inversion approach, we solved for three ecophysiological parameters of the northern biosphere (^(13)C discrimination, a net primary production light use efficiency, and a temperature sensitivity of heterotrophic respiration (a Q10 factor)) that provided a best fit between modeled and observed ή^(13)C and CO_2. In our analysis we attempted to explicitly correct for fossil fuel emissions, remote C4 ecosystem fluxes, ocean exchange, and isotopic disequilibria of terrestrial heterotrophic respiration caused by the Suess effect. We obtained a photosynthetic discrimination for arctic and boreal biomes between 19.0 and 19.6‰. Our inversion analysis suggests that Q10 and light use efficiency values that minimize the cost function covary. The optimal light use efficiency was 0.47 gC MJ^(−1) photosynthetically active radiation, and the optimal Q10 value was 1.52. Fossil fuel and ocean exchange contributed proportionally more to month-to-month changes in the atmospheric growth rate of ή^(13)C and CO_2 during winter months, suggesting that remote atmospheric observations during the summer may yield more precise estimates of the isotopic composition of the biosphere

    L’effet de l’obĂ©sitĂ© paternelle acquise sur la biologie des spermatozoĂŻdes, la cinĂ©tique de division embryonnaire, et sur l’hĂ©rĂ©ditĂ© transgĂ©nĂ©rationelle

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    Obesity is a medical condition resulting from an excessive accumulation of adipose deposits. The pathological remodelling of the adipose tissue in obese subjects may lead to the development of several health problems. Unfortunately, the prevalence of obesity is increasing worldwide and of particular interest among young men of reproductive age. Furthermore, accumulated evidence suggests that information from paternal environment such as acquired obesity remains in the sperm epigenome and can modulate the phenotype of the offspring. Therefore, a deeper comprehension of the drawbacks of male excessive fatness on the sperm molecular composition is needed. The first aim of this thesis was to assess the impact of obesity on the molecular composition and on the physiology of the motile sperm. The semen samples were obtained from 96 men attending the A-clinic fertility center, Lebanon. Patients were categorized into three groups: normal weight, overweight, and obese. We showed that the motile sperm of obese men had abnormal levels of paternally inherited histones and hypomethylated/hypohydroxymethylated DNA as compared to normal weight men. Subsequently, the embryos derived from the motile sperm of an obese father had an altered morphokinetic patterns when compared to those derived from normal weight one. The second aim of this thesis was to evaluate the adaptive and evolutionary potential of non-genetic heritable mechanisms in experimentally controlled animal models. Using a high fat diet (HFD)-induced obesity mouse model, we have examined how feeding male mice with a high fat diet for multiple generations impacts the phenotype of the resulting miceL'obĂ©sitĂ© est une condition mĂ©dicale rĂ©sultant d'une accumulation excessive de dĂ©pĂŽts adipeux. Le remodelage pathologique du tissu adipeux chez les sujets obĂšses pourrait conduire Ă  l'Ă©laboration de plusieurs problĂšmes de santĂ©. Malheureusement, la prĂ©valence de l'obĂ©sitĂ© augmente dans le monde entier et en particulier chez les jeunes hommes en Ăąge de procrĂ©ation. En outre, plusieurs Ă©tudes ont suggĂ©rĂ© que les informations de l'environnement paternel comme l'obĂ©sitĂ© acquise restent dans l’épigĂ©nome du spermatozoĂŻde et peuvent moduler le phĂ©notype de la descendance. Pour toutes ces raisons, une comprĂ©hension plus approfondie des effets de l’obĂ©sitĂ© sur la composition molĂ©culaire des spermatozoĂŻdes est nĂ©cessaire. Le premier objectif de cette thĂšse Ă©tait d'Ă©valuer l'effet de l'obĂ©sitĂ© sur la composition molĂ©culaire et sur la physiologie des spermatozoĂŻdes mobiles. Les Ă©chantillons de sperme ont Ă©tĂ© obtenus Ă  partir de 96 hommes s’adressant au centre de fertilitĂ© ‘A-clinic’, Liban. Les patients ont Ă©tĂ© classĂ©s en trois groupes : poids normal, le surpoids, et obĂšses. Nos rĂ©sultats ont montrĂ© qu’il y a une rĂ©tention des histones plus Ă©levĂ©e, et un ADN spermatique hypomĂ©thylĂ© et hypohydroxymethylĂ©, dans les spermatozoĂŻdes mobiles des hommes obĂšses par rapport Ă  ceux des hommes non-obeses. Par consĂ©quent, les embryons issus de spermatozoĂŻdes mobiles d'un homme obĂšse avaient une cinĂ©tique de division embryonnaire altĂ©rer par rapport Ă  ceux provenant des spermatozoĂŻdes d’un homme de poids norma
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