Éditeur(s) : HAL CCSD AGU and the Geochemical Society
Résumé : International audience
Numerical models show that small-scale convection (SSC) occurring atop a mantle plume is a plausible mechanism to rejuvenate the lithosphere. The triggering of SSC depends on the density contrast and on the rheology of the unstable layer underlying the stagnant upper part of the thermal boundary layer (TBL). Partial melting may change both properties. We analyze, using 2-D numerical simulations, how partial melting influences the dynamics of time-dependent SSC instabilities and the resulting thermo-mechanical rejuvenation of an oceanic plate moving atop of a plume. Our simulations show a complex behavior, with acceleration, no change, or delay of the SSC onset, due to competing effects of the latent heat of partial melting, which cools the plume material, and of the buoyancy increase associated with both melt retention and depletion of residue following melt extraction. The melt-induced viscosity reduction is too localized to affect significantly SSC dynamics. Faster SSC triggering is promoted for low melting degrees (low plume temperature anomalies, thick lithosphere, or fast moving plates), which limit both the temperature reduction due to latent heat of melting and the accumulation of depleted buoyant residue in the upper part of the unstable layer. In contrast, high partial melting degrees lead to a strong temperate decrease due to latent heat of melting and development of a thick depleted layer within the sublithospheric convecting layer, which delay the development of gravitational instabilities. Despite differences in SSC dynamics, the thinning of the lithosphere is not significantly enhanced relatively to simulations that neglect partial melting.
ISSN: 1525-2027

hal-01277175
https://hal.archives-ouvertes.fr/hal-01277175
DOI : 10.1002/2015GC005967

Éditeur(s) : HAL CCSD Landes Bioscience
Résumé : International audience
In 2008 we published the first set of guidelines for standardizing research in autophagy. Since then, research on this topic has continued to accelerate, and many new scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Accordingly, it is important to update these guidelines for monitoring autophagy in different organisms. Various reviews have described the range of assays that have been used for this purpose. Nevertheless, there continues to be confusion regarding acceptable methods to measure autophagy, especially in multicellular eukaryotes. A key point that needs to be emphasized is that there is a difference between measurements that monitor the numbers or volume of autophagic elements (e.g., autophagosomes or autolysosomes) at any stage of the autophagic process vs. those that measure flux through the autophagy pathway (i.e., the complete process); thus, a block in macroautophagy that results in autophagosome accumulation needs to be differentiated from stimuli that result in increased autophagic activity, defined as increased autophagy induction coupled with increased delivery to, and degradation within, lysosomes (in most higher eukaryotes and some protists such as Dictyostelium) or the vacuole (in plants and fungi). In other words, it is especially important that investigators new to the field understand that the appearance of more autophagosomes does not necessarily equate with more autophagy. In fact, in many cases, autophagosomes accumulate because of a block in trafficking to lysosomes without a concomitant change in autophagosome biogenesis, whereas an increase in autolysosomes may reflect a reduction in degradative activity. Here, we present a set of guidelines for the selection and interpretation of methods for use by investigators who aim to examine macroautophagy and related processes, as well as for reviewers who need to provide realistic and reasonable critiques of papers that are focused on these processes. These guidelines are not meant to be a formulaic set of rules, because the appropriate assays depend in part on the question being asked and the system being used. In addition, we emphasize that no individual assay is guaranteed to be the most appropriate one in every situation, and we strongly recommend the use of multiple assays to monitor autophagy. In these guidelines, we consider these various methods of assessing autophagy and what information can, or cannot, be obtained from them. Finally, by discussing the merits and limits of particular autophagy assays, we hope to encourage technical innovation in the field.
Autophagy

hal-00735751
https://hal.archives-ouvertes.fr/hal-00735751
PUBMED : 22966490

Résumé : Publiée dans le cadre du premier Congrès international d'histoire coloniale à Paris
Siècle(s) traité(s) : 20
Droits : Domaine public
Provenance : Ville de Pointe-à-Pitre. Réseau des bibliothèques
Permalien : http://www.manioc.org/patrimon/PAP11103
PAP11103

Éditeur(s) : Paris : Imprimerie nationale
Siècle(s) traité(s) : 19
Droits : Domaine public
Provenance : Collectivité territoriale de Martinique. Bibliothèque Schoelcher
Permalien : http://www.manioc.org/patrimon/SCH13175
SCH13175

Éditeur(s) : La Habana : Imprenta "La Universal"

Droits : Domaine public
Provenance : Institut des Hautes Études de l'Amérique latine, Bibliothèque Pierre-Monbeig
Permalien : http://www.manioc.org/patrimon/IHE14021
IHE14021

Éditeur(s) : Paris : Typographie de Firmin Didot frères
Extrait de : Dépôt Général de la marine

Droits : Domaine public
Provenance : Université de Nantes. Service commun de la documentation
Permalien : http://www.manioc.org/patrimon/NAN13016-2
NAN13016-2

Éditeur(s) : Paris : Marpon et Flammarion
Siècle(s) traité(s) : 19
Droits : Domaine public
Provenance : Ville de Pointe-à-Pitre. Réseau des bibliothèques
Permalien : http://www.manioc.org/patrimon/PAP11088
PAP11088

Éditeur(s) : Londres : P. S. King and Son
Siècle(s) traité(s) : 19
Provenance : Université Caen Normandie. Service commun de la documentation
Permalien : http://www.manioc.org/patrimon/CAE19037
CAE19037