Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
Laboratory models have been conducted to improve our understanding of the role that the resistance of the slab to bending and its coupling to the ambient mantle play in subduction dynamics over geological time scales. Our models are set up with a viscous plate of silicone (lithosphere) subducting under negative buoyancy in a viscous layer of glucose syrup (mantle). For our study, the lithosphere/upper mantle viscosity contrast has been systematically varied, from similar to 10 to similar to 10(5) in order to explore the parameter space between weak and strong slab dynamics. We found that subduction is characterized by a retreating mode for viscosity ratios > 10(4), by the coexistence of a retreating mode and an advancing mode for viscosity ratios between similar to 10(4) and similar to 10(2), and quasi-stationary, Rayleigh-Taylor like behaviour for ratios < 10(2). By combining our experimental results and kinematic data from current subduction zones in four reference frames which differ in the amount of net rotation, we infer that a lithosphere/upper mantle viscosity contrast of 150-500 is necessary to obtain realistic trench/subducting plate velocity ratios as well as the variability of subduction styles observed in nature.
ISSN: 0012-821X

hal-00412008
https://hal.archives-ouvertes.fr/hal-00412008
DOI : 10.1016/j.epsl.2008.04.006

Éditeur(s) : HAL CCSD IOS Press
Résumé : International audience
The hematocrit-to-viscosity ratio (HVR) has been widely used has an estimate of red blood cell (RBC) oxygen transport effectiveness into the microvasculature or as an oxygen delivery index. However, no study investigated the possibility of HVR to truly reflect RBC oxygen transport effectiveness or to be an oxygen delivery index. We measured blood viscosity at high shear rate (225 s-1), hematocrit, HVR, as well as the microvascular oxyhemoglobin saturation (TOI; tissue oxygen index) by spatial resolved near-infrared spectroscopy (NIRS) at cerebral and muscle levels in three population known to have various degrees of hemorheological abnormalities: healthy subjects (AA), patients with sickle cell SC disease (SC) characterized by moderate anemia and patients with sickle cell anemia (SS) marked by severe anemia. At both the cerebral and muscle level, HVR was positively correlated with TOI (r = 0.28; p = 0.03 and r = 0.38; p = 0.003, at the cerebral and muscle level, respectively). These findings suggest that HVR probably play a key role in blood flow and hemodynamic regulation in the microvasculature, hence modulating the amount of oxygen available for tissues. Nevertheless, the strengths of the associations are weak (R2 < 0.50), suggesting that other determinants modulate microvascular blood flow and oxygenation, such as vascular geometry and vasomotor reserve.
ISSN: 1386-0291

inserm-01081701
http://www.hal.inserm.fr/inserm-01081701
http://www.hal.inserm.fr/inserm-01081701/document
http://www.hal.inserm.fr/inserm-01081701/file/2013%2C%20Waltz%20-%20Is%20there%20a%20relationship%20between%20the%20hematocrit-to-viscosity%20ratio%20and%20microvascular%20oxygenation%20in%20brain%20and%20muscle.pdf
PUBMED : 23719422

Éditeur(s) : Gauthier-Villars
Résumé : Simple thermodynamics calculations are applied to processes of a rising plume within an environment of an upward directed gradient of viscosity in the uppermost mantle. Four stages of the development of passive margins are described. Following an initial regional uplift strong lateral movements are induced at asthenospheric levels, stretching the overlying lithosphere. In the second stage plume material also enters the low viscosity lower crust, replacing continental material and forming a new, higher crust-mantle boundary by gravitational differentiation. The inital phase lag between the laterally intruding plume material and the rest of the lithosphere disappears once the continent is rifted and sea floor spreading is established (= stage 3). Finally, at stage 4, quiet subsidence, controlled by contraction, sedimentation, and possible phase changes in the lower crust, is established. The sequence described is in accordance with many observations of geology and geophysics. Rising plumes and sinking slabs are considered equivalent expressions of the heat engine earth which determines global tectonics.
Oceanologica Acta, Special issue (0399-1784) (Gauthier-Villars), 1981

Droits : info:eu-repo/semantics/openAccess
http://archimer.ifremer.fr/doc/00245/35658/34167.pdf
http://archimer.ifremer.fr/doc/00245/35658/

Éditeur(s) : Springer
Résumé : The French Atlantic coast contains large highly productive intertidal mudflats that are colonised by juveniles of numerous flatfish species, including the common sole (Solea solea, L.). These ecosystems are also heavily exploited by the shellfish farming industry. Intensive bivalve culture is associated with substantial biodeposition (1-6 t-dw ha(-1) day(-1)), which directly or indirectly contributes to increase exopolysaccharide (EPS) concentrations at the interface between water column and seabed. EPS are long-chain molecules organised into colloids, which influence rheological properties of water, particularly viscosity. Increased water viscosity had consequences for ventilatory activity of juvenile flatfish, whereby the minimal pressure required to ventilate the medium increases directly with EPS concentration. Moreover, the critical EPS concentration ([EPS](crit)) at which water was no longer able to flow through the branchial basket ranged from almost nil to over 30 mg l(-1), depending on species and size. [EPS](crit) was lower in small individuals and individuals from species with high metabolic rates (turbot and plaice). These differences may depend upon gill and bucco-branchial cavity morphometrics. The ventilatory workload of sole increased with viscosity to a maximum at 2 mg EPS l(-1). Viscosity might, therefore, be a limiting factor for flatfish post larvae, which colonise the intertidal mudflats, depending upon their size and species. EPS concentrations in the field can reach 15 mg l(-1). A selective effect is conceivable but remains to be estimated in the field.
Marine Biology (0025-3162) (Springer), 2007-09 , Vol. 152 , N. 4 , P. 803-814

Droits : 2007 Springer
http://archimer.ifremer.fr/doc/2007/publication-2801.pdf
DOI:10.1007/s00227-007-0731-z
http://archimer.ifremer.fr/doc/00000/2801/

Éditeur(s) : HAL CCSD Ferrata Storti Foundation
Résumé : International audience
BackgroundRecent evidence suggests that autonomic nervous system activity could be involved in thepathophysiology of sickle cell disease, but it is unclear whether differences in autonomic nervoussystem activity are detectable during steady state in patients with mild and severe disease.The aim of the present study was to compare the autonomic nervous system activity, bloodrheology, and inflammation in patients with sickle cell anemia according to the frequency ofacute pain crisis.Design and MethodsTwenty-four healthy volunteers, 20 patients with sickle cell anemia with milder disease, and15 patients with sickle cell anemia with more severe disease were recruited. Milder disease wasdefined as having no pain crisis within the previous year. More severe disease was defined ashaving had within the previous year three or more pain crises which were documented by aphysician and required treatment with narcotics. The autonomic nervous system activity wasdetermined by spectral analysis of nocturnal heart rate variability. Blood viscosity determinationand measurements of several inflammatory markers (interleukin-6, soluble vascular celladhesion molecule-1, soluble CD40 ligand and sL-selectin) were made on blood samples collectedin steady-state conditions.ResultsResults showed that: 1) patients who had suffered more frequent pain crises had lowerparasympathetic activity and greater sympatho-vagal imbalance than both controls andpatients with milder disease. However, when adjusted for age, no significant difference wasdetected between the two sickle cell anemia patient groups; 2) patients who had suffered morefrequent pain crises had higher blood viscosity than patients with milder disease, and this wasnot dependent on age.ConclusionsResults from the present study indicate that both the autonomic nervous system activity andblood viscosity are impaired in patients with sickle cell anemia exhibiting high frequency ofpain crisis in comparison with those who did not experience a crisis within the previous year.
ISSN: 0390-6078

hal-01163973
https://hal.univ-antilles.fr/hal-01163973
DOI : 10.3324/haematol.2011.047365

Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
The origin of plate tectonics is one of the most fundamental issues in earth and planetary sciences. Laboratory experiments indicate that the viscosity of silicate rocks is so strongly temperature-dependent that the entire surface of the Earth should be one immobile rigid plate. The rheology of oceanic lithosphere is, however, still poorly understood, and there exist few constraints on the temperature dependency of viscosity on the field scale. Here we report a new kind of observational constraint based on the geoid along oceanic fracture zones. We identify a large number of conspicuous small-scale geoid anomalies, which cannot be explained by the standard evolution model of oceanic lithosphere, and estimate their source density perturbations using a new Bayesian inversion method. Our results suggest that they are caused most likely by small-scale convection involving temperature perturbations of ∼300 K±100 K∼300 K±100 K. Such thermal contrast requires the activation energy of mantle viscosity to be as low as View the MathML source100±50 kJmol−1 in case of diffusion creep, and View the MathML source225±112 kJmol−1 in case of dislocation creep, substantially reducing the thickness of the stiffest part of oceanic lithosphere. Oceanic lithosphere may thus be broken and bent much more easily than previously thought, facilitating the operation of plate tectonics.
ISSN: 0012-821X

hal-01467827
https://hal.archives-ouvertes.fr/hal-01467827
DOI : 10.1016/j.epsl.2016.05.027

Éditeur(s) : HAL CCSD Public Library of Science
Résumé : International audience
Patients with sickle cell anemia (SCA) have usually lower diastolic, systolic and mean blood pressure (BP) than the general population. However, BP values ≥120/70 mmHg considerably increase the risk for acute and chronic complications in SCA. The aim of this study was to identify biological factors associated with relative hypertension in adults with SCA. We compared the hematological, lipid and hemolytic profiles, as well as blood viscosity, between SCA patients with normal BP (<120/70 mmHg, n = 54) and those with relative hypertension (BP≥120/70 mmHg, n = 43). Our results demonstrated that male gender (OR: 3.49; 95%CI 1.20 to 10.16, p<0.05), triglycerides (OR: 9.19; 95% CI 2.29 to 36.95, p<0.01), blood viscosity (OR: 1.35; 95% CI 1.01 to 1.81, p<0.05) and body mass index (OR: 1.37; 95% CI 1.14 to 1.64, p<0.01) were independent risks factors for relative hypertension in SCA. No association was found between the BP status and the positive history of painful vaso-occlusive crisis or acute chest syndrome. An association between triglycerides level and the occurrence of these two major acute complications was detected. Our study suggests that male gender, increased triglycerides level, BMI and blood viscosity could increase the risk for developing relative hypertension in SCA. In addition, our results support a role of moderately elevated triglycerides in the pathophysiology of vaso-occlusive events.
ISSN: 1932-6203

inserm-00838991
http://www.hal.inserm.fr/inserm-00838991
http://www.hal.inserm.fr/inserm-00838991/document
http://www.hal.inserm.fr/inserm-00838991/file/Lamarre_et_al._2013_PloS_ONE_.pdf
DOI : 10.1371/journal.pone.0066004

Résumé : Hierba anual, erguida, leñosa en la base, de hasta 3 o 4 m, no ramificada. Hojas orbiculares, de 10-30 cm, 5-7 lobadas; lóbulos lanceolados a aovados aserrados, agudos u obtusos. Cáliz de 2 cm, pétalos amarillos con manchas purpúreas en el centro, de 3-4 cm. Fruto capsular anguloso de hasta 20 cm, acuminada, viscosa.
Herbacée annuelle, ligneuse à la base, pouvant atteindre 3-4 mètres, sans ramifications. Feuilles orbiculaires, de 10 à 30 cm, 5-7 lobulées; lobules de lancéolés à ovoïdes dentelés, aigus ou obtus. Fleur à calice de 2 cm, pétales jaunes avec taches pourpres au centre, de 3-4 cm. Fruit capsulaire anguleux pouvant atteindre 20 cm, acuminé, visqueux.
Erect undershrub2-4 m high. Leaves orbicular and lobed 10-30 cm long; lanceolate to obovate, acute or obtuse; calyx 2 cm long, yellow corolla with a 3-4 cm purple area at the base; angular capsule (fruit), up to 20 cm long.
Originario del Viejo Mundo. Cultivada en las regiones tropicales y subtropicales.
Plante originaire de l';Ancien Monde; cultivée dans les régions tropicales et subtropicales.
Native to the Old World.  Cultivated in tropical and subtr

http://www.tramil.net/fototeca/plant1

Éditeur(s) : HAL CCSD Public Library of Science
Résumé : International audience
Leg ulcer is a disabling complication in patients with sickle cell anemia (SCA) but the exact pathophysiological mechanisms are unknown. The aim of this study was to identify the hematological and hemorheological alterations associated with recurrent leg ulcers. Sixty-two SCA patients who never experienced leg ulcers (ULC-) and 13 SCA patients with a positive history of recurrent leg ulcers (ULC+) - but with no leg ulcers at the time of the study - were recruited. All patients were in steady state condition. Blood was sampled to perform hematological, biochemical (hemolytic markers) and hemorheological analyses (blood viscosity, red blood cell deformability and aggregation properties). The hematocrit-to-viscosity ratio (HVR), which reflects the red blood cell oxygen transport efficiency, was calculated for each subject. Patients from the ULC+ group were older than patients from the ULC- group. Anemia (red blood cell count, hematocrit and hemoglobin levels) was more pronounced in the ULC+ group. Lactate dehydrogenase level was higher in the ULC+ group than in the ULC- group. Neither blood viscosity, nor RBC aggregation properties differed between the two groups. HVR was lower and RBC deformability tended to be reduced in the ULC+ group. Our study confirmed increased hemolytic rate and anemia in SCA patients with leg ulcers recurrence. Furthermore, our data suggest that although systemic blood viscosity is not a major factor involved in the pathophysiology of this complication, decreased red blood cell oxygen transport efficiency (i.e., low hematocrit/viscosity ratio) may play a role.
ISSN: 1932-6203

inserm-00922105
http://www.hal.inserm.fr/inserm-00922105
http://www.hal.inserm.fr/inserm-00922105/document
http://www.hal.inserm.fr/inserm-00922105/file/2013_Connes_-_Decreased_Hematocrit.pdf
DOI : 10.1371/journal.pone.0079680

Éditeur(s) : HAL CCSD IOS Press
Résumé : International audience
The hematocrit-to-viscosity ratio (HVR) has been widely used has an estimate of red blood cell (RBC) oxygen transport effectiveness into the microvasculature or as an oxygen delivery index. However, no study investigated the possibility of HVR to truly reflect RBC oxygen transport effectiveness or to be an oxygen delivery index. We measured blood viscosity at high shear rate (225 s −1), hematocrit, HVR, as well as the microvascular oxyhemoglobin saturation (TOI; tissue oxygen index) by spatial resolved near-infrared spectroscopy (NIRS) at cerebral and muscle levels in three population known to have various degrees of hemorheological abnormalities: healthy subjects (AA), patients with sickle cell SC disease (SC) characterized by moderate anemia and patients with sickle cell anemia (SS) marked by severe anemia. At both the cerebral and muscle level, HVR was positively correlated with TOI (r = 0.28; p = 0.03 and r = 0.38; p = 0.003, at the cerebral and muscle level, respectively). These findings suggest that HVR probably play a key role in blood flow and hemodynamic regulation in the microvasculature, hence modulating the amount of oxygen available for tissues. Nevertheless, the strengths of the associations are weak (R 2 < 0.50), suggesting that other determinants modulate microvascular blood flow and oxygenation, such as vascular geometry and vasomotor reserve.
ISSN: 1386-0291

hal-01163460
https://hal.univ-antilles.fr/hal-01163460
DOI : 10.3233/CH-131742

Éditeur(s) : HAL CCSD IOS Press
Résumé : International audience
Little is known about the impact of blood rheology on the occurrence of retinopathy in sickle cell disease (SCD). Fifty-nine adult SCD patients in steady-state condition participated to the study: 32 with homozygous SCD (sickle cell anemia; SCA) and 27 with sickle cell hemoglobin-C disease (SCC). The patients underwent retinal examination and were categorized according to the classification of Goldberg: 1) no retinopathy (group 1), 2) non-proliferative or proliferative stage I-II retinopathy (group 2) and 3) proliferative stage III-IV-V retinopathy (group 3). Hematological and hemorheological (whole blood viscosity, RBC deformability and aggregation properties) measurements were performed for each patient. In the whole SCD group (SCA + SCC patients) and in SCC patients, the group 3 had higher platelets count than group 2 but the difference between group 3 and group 1 did not reach statistical significance. No difference was observed for the other parameters between the three groups. SCC patients from the group 3 exhibited higher whole blood viscosity than SCC patients from the group 1. No significant difference was observed between the three groups in SCA patients. This study revealed that severe sickle proliferative retinopathy is associated with blood hyperviscosity in SCC patients but not in SCA patients.
ISSN: 1386-0291

inserm-00849032
http://www.hal.inserm.fr/inserm-00849032
http://www.hal.inserm.fr/inserm-00849032/document
http://www.hal.inserm.fr/inserm-00849032/file/inserm-00849032.pdf
DOI : 10.3233/CH-2012-1622

Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
Vascular resistance and tissue perfusion may be both affected by impaired vascular function and increased blood viscosity. Little is known about the effects of vascular function on the occurrence of painful vaso-occlusive crises (VOC) in children with sickle cell anemia (SCA). The aim of the present study was to determine which side of the balance (blood viscosity or vascular function) is the most deleterious in SCA and increases the risk for frequent hospitalized VOC. Microvascular function, microcirculatory oxygenation and blood viscosity were determined in a group of 22 SCA children/adolescents at steady state and a group of 13 healthy children/adolescents. Univariate analyses demonstrated blunted microvascular reactivity during local thermal heating test and decreased microcirculatory oxygenation in SCA children compared to controls. Multivariate analysis revealed that increased blood viscosity and decreased microcirculatory oxygenation were independent risk factors of frequent VOC in SCA. In contrast, the level of microvascular dysfunction does not predict VOC rate. In conclusion, increased blood viscosity is usually well supported in healthy individuals where vascular function is not impaired. However, in the context of SCA, microvascular function is impaired and any increase of blood viscosity or decrease in microcirculatory oxygenation would increase the risks for frequent VOC.
ISSN: 1079-9796

hal-01668335
https://hal.univ-antilles.fr/hal-01668335
DOI : 10.1016/j.bcmd.2015.10.005

Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
Although subducting slabs undergo a bending deformation that resists tectonic plate motions, the magnitude of this resistance is not known because of poor constraints on slab strength. However, because slab bending slows the relatively rapid motions of oceanic plates, observed plate motions constrain the importance of bending. We estimated the slab pull force and the bending resistance globally for 207 subduction zone transects using new measurements of the bending curvature determined from slab seismicity. Predicting plate motions Using a global mantle flow model, we constrain the viscosity of the bending slab to be at most similar to 300 times more viscous than the upper mantle: stronger slabs are intolerably slowed by the bending deformation. Weaker slabs, however, cannot transmit a pull force sufficient to explain rapid trenchward plate motions unless slabs stretch faster than seismically observed rates of similar to 10(-15) s(-1). The constrained bending viscosity (similar to 2 x 10(23) Pa s) is larger than previous estimates that yielded similar or larger bending resistance (here similar to 25% of forces). This apparent discrepancy occurs because slabs bend more gently than previously thought, with an average radius of curvature of 390 km that permits subduction Of Strong slabs. This gentle bending may ultimately permit plate tectonics on Earth.
ISSN: 0012-821X

hal-00412383
https://hal.archives-ouvertes.fr/hal-00412383
DOI : 10.1016/j.epsl.2008.05.009

Résumé : Nous avons étudié les marqueurs hémorhéologiques, hématologiques et biochimiques chez des sujets drépanocytaires homozygotes SS (HbS/HbS) et hétérozygotes composites SC (HbS/HbC) dans deux cohortes, pédiatriques et adultes, de patients drépanocytaires, et ce, à travers 7 complications récurrentes de la drépanocytose : 2 appartenant au profil hémolytique (l’ulcère de jambes et la glomérulopathie) et 5 appartenant au phénotype visqueux/vaso-occlusif (l’hypertension artérielle, le syndrome thoracique aigu (STA), la crise vaso-occlusive (CVO), la rétinopathie et l’ostéonécrose). Nous avons montré que : 1) une viscosité sanguine et une déformabilité érythrocytaire élevées sont des facteurs de risques de CVO chez les enfants homozygotes ; 2) Une viscosité sanguine élevée est associée à une hypertension artérielle systémique relative chez des adultes SS ; 3) les enfants SC présente une fonction vasculaire mieux préservée que les enfants SS pour faire face à une augmentation de la viscosité sanguine ; 4) les patients adultes SS avec une ostéonécrose présentent une déformabilité érythrocytaire plus élevée que les patients sans ostéonécrose ; 5) une viscosité sanguine élevée est associée à la présence d’une rétinopathie chez les adultes SC mais pas chez les SS ; 6) les patients adultes SS présentant une glomérulopathie ont un taux d’hémolyse élevé, une déformabilité érythrocytaire réduite et des agrégats érythrocytaires très robustes ; 7) les patients adultes SS avec des ulcères de jambes récurrents ont un taux d’hémolyse accru et une déformabilité érythrocytaire réduite. De plus, nos travaux confirment que l’-thalassémie module les propriétés de déformabilité érythrocytaire, mais montrent pour la première fois qu’elle module aussi les propriétés d’agrégation érythrocytaire, et notamment la force des agrégats érythrocytaires. En conclusion, ces travaux permettent de préciser le rôle de la rhéologie sanguine dans un certain nombre de complications de la drépanocytose et d’enrichir le modèle préexistant divisant les complications de la drépanocytose selon 2 phénotypes : hémolytique versus visqueux/vaso-occlusif. Nous montrons pour la première fois que le phénotype hémolytique est caractérisé aussi par des anomalies de la rhéologie du globule rouge : rigidité accrue et agrégats érythrocytaire robustes.
Hemorheological, hemathological, and biochemical marquers of patients with sickle cell anemia (SS) and patients with sickle cell SC disease (SC) were studied in 2 cohorts: children and adults. We focused on 7 recurrent complications: 5 belonging to the viscosity/vaso-occlusion phenotype (systemic hypertension, acute chest syndrome (ACS), vaso-occlusive crisis (VOC), retinopathy and osteonecrosis) and 2 belonging to the hemolytic phenotype (leg ulcer and glomerulopathy). Our results show that 1) high viscosity is associated with increased risk for VOC in SS children; 2) blood viscosity is increased in SS adults with systemic relative hypertension; 3) SC children have preserved vascular function compared to SS children; 4) SS adults with osteonecrosis are characterized by higher red blood cell (RBC) deformability than SS adults without osteonecrosis; 5) high blood viscosity is associated with retinopathy in SC adults but not in SS adults; 6) SS adults affected by glomerulopathy have high hemolytic rate, low RBC deformability and increased RBC aggregates strenght; 7) SS adults with recurrent leg ulcers have high hemolytic rate and reduced RBC deformability. Moreover, our studies shows that alpha-thalassemia modulate RBC deformability and RBC aggregation properties. In conclusion, this work shows for the first time that the hemolytic phenotype is characterized by an abnormal RBC rheology which may play a role in several sickle cell complications.

http://www.theses.fr/2013AGUY0684/document

Éditeur(s) : HAL CCSD European Geosciences Union
Résumé : The properties of the subduction interplate domain are likely to affect not only the seismogenic potential of the subduction area but also the overall subduction process, as it influences its viability. Numerical simulations are performed to model the long-term equilibrium state of the subduction interplate when the diving lithosphere interacts with both the overriding plate and the surrounding convective mantle. The thermomechanical model combines a non-Newtonian viscous rheology and a pseudo-brittle rheology. Rock strength here depends on depth, temperature and stress, for both oceanic crust and mantle rocks. I study the evolution through time of, on one hand, the brittle-ductile transition (BDT) depth, zBDT, and, on the other hand, of the kinematic decoupling depth, zdec, simulated along the subduction interplate. The results show that both a high friction and a low ductile strength at the asthenospheric wedge tip shallow zBDT. The influence of the weak material activation energy is of second order but not negligible. zBDT becomes dependent on the ductile strength increase with depth (activation volume) if the BDT occurs at the interplate decoupling depth. Regarding the interplate decoupling depth, it is shallowed (1) significantly if mantle viscosity at asthenospheric wedge tip is low, (2) if the difference in mantle and interplate activation energy is weak, and (3) if the activation volume is increased. Very low friction coefficients and/or low asthenospheric viscosities promote zBDT = zdec. I then present how the subducting lithosphere age affects the brittle-ductile transition depth and the kinematic decoupling depth in this model. Simulations show that a rheological model in which the respective activation energies of mantle and interplate material are too close hinders the mechanical decoupling at the down-dip extent of the interplate, and eventually jams the subduction process during incipient subduction of a young (20-Myr-old) and soft lithosphere under a thick upper plate. Finally, both the BDT depth and the decoupling depth are a function of the subducting plate age, but are not influenced in the same fashion: cool and old subducting plates deepen the BDT but shallow the interplate decoupling depth. Even if BDT and kinematic decoupling are intrinsically related to different mechanisms of deformation, this work shows that they are able to interact closely. Comparison between modelling results and observations suggests a minimum friction coefficient of 0.045 for the interplate plane, even 0.069 in some cases, to model realistic BDT depths. The modelled zdec is a bit deeper than suggested by geophysical observations. Eventually, the better way to improve the adjustment to observations may rely on a moderate to strong asthenosphere viscosity reduction in the metasomatised mantle wedge.
ISSN: 1869-9510

hal-00795559
https://hal.archives-ouvertes.fr/hal-00795559
DOI : 10.5194/se-3-467-2012, 2012

Éditeur(s) : HAL CCSD IOS Press
Résumé : International audience
Patients with hemoglobin C disease (CC) usually do not develop severe complications in comparison with individuals with sickle cell anemia (SS) or with sickle cell hemoglobin C disease (SC). The present study compared the hematological, biochemical, hemorheological and clinical characteristics of CC patients to those of SS, SC and healthy individuals (AA). Blood viscosity was measured at 225 s(-1) with a cone plate viscometer. The hematocrit-to-blood viscosity ratio (HVR), i.e. an index of red blood cell (RBC) oxygen transport effectiveness, was calculated. RBC deformability was determined at 30 Pa by ektacytometry, and RBC aggregation properties by syllectometry. CC and SC had higher blood viscosity and lower HVR than AA. Nevertheless, HVR was higher in CC compared to SS and tended to be higher than in SC. The CC group exhibited very rigid hyperchromic RBC compared to the three other groups. RBC aggregation abnormalities were observed in CC: low RBC aggregation index and high RBC aggregates strength. Despite these hemorheological abnormalities, CC never had hospitalized painful vaso-occlusive crisis or acute chest syndrome. In contrast, all of them had splenomegaly. Of note, 2 out of 7 CC developed retinopathy or otologic disorders. Whether the blood hyperviscosity and decreased RBC deformability are responsible for these complications is unknown. The higher oxygen transport effectiveness (i.e., HVR) of CC compared to SS is probably at the origin of the very low risk of medical complication in this population.
ISSN: 1386-0291

hal-01668336
https://hal.univ-antilles.fr/hal-01668336
DOI : 10.3233/CH-141906

Éditeur(s) : HAL CCSD
Résumé : International audience
As subducting plates reach the base of the upper mantle, some appear to flatten and stagnate, while others seemingly go through unimpeded. This variable resistance to slab sinking has been proposed to affect long-term thermal and chemical mantle circulation. A review of observational constraints and dynamic models highlights that neither the increase in viscosity between upper and lower mantle (likely by a factor 20–50) nor the coincident endothermic phase transition in the main mantle silicates (with a likely Clapeyron slope of –1 to –2 MPa/K) suffice to stagnate slabs. However, together the two provide enough resistance to temporarily stagnate subducting plates, if they subduct accompanied by significant trench retreat. Older, stronger plates are more capable of inducing trench retreat, explaining why backarc spreading and flat slabs tend to be associated with old-plate subduction. Slab viscosities that are ∼2 orders of magnitude higher than background mantle (effective yield stresses of 100–300 MPa) lead to similar styles of deformation as those revealed by seismic tomography and slab earthquakes. None of the current transition-zone slabs seem to have stagnated there more than 60 m.y. Since modeled slab destabilization takes more than 100 m.y., lower-mantle entry is apparently usually triggered (e.g., by changes in plate buoyancy). Many of the complex morphologies of lower-mantle slabs can be the result of sinking and subsequent deformation of originally stagnated slabs, which can retain flat morphologies in the top of the lower mantle, fold as they sink deeper, and eventually form bulky shapes in the deep mantle.
ISSN: 1553-040X

hal-01571965
https://hal.archives-ouvertes.fr/hal-01571965
DOI : 10.1130/GES01476.1

Éditeur(s) : HAL CCSD Oxford University Press (OUP)
Résumé : International audience
Two-dimensional simulations using a thermomechanical model based on a finite-difference method on a staggered grid and a marker in cell method are performed to study the plume-lithosphere interaction beneath moving plates. The plate and the convective mantle are modelled as a homogeneous peridotite with a Newtonian temperature- and pressure-dependent viscosity. A constant velocity, ranging from 5 to 12.5 cm yr−1, is imposed at the top of the plate. Plumes are generated by imposing a thermal anomaly of 150 to 350 K on a 50 km wide domain at the base of the model (700 km depth); the plate atop this thermal anomaly is 40 Myr old. We analyse (1) the kinematics of the plume as it impacts the moving plate, (2) the dynamics of time-dependent small-scale convection (SSC) instabilities developing in the low-viscosity layer formed by spreading of hot plume material at the base of the lithosphere and (3) the resulting thermal rejuvenation of the lithosphere. The spreading of the plume material at the base of the lithosphere, characterized by the ratio between the maximum down- and upstream horizontal (dimensionless) velocities in the plume-fed sublithospheric layer, Peup/Pedown depends on the ratio between the maximum plume upwelling velocity and the plate velocity, Peplume/Peplate. For fast plate velocities and sluggish plumes (low Peplume/Peplate), plate motion drags most plume material and downstream flow is dominant. As Peplume/Peplate increases, an increasing part of the plume material flows upstream. SSC systematically develops in the plume-fed sublithospheric layer, downstream from the plume. Onset time of SSC decreases with the Rayleigh number. For vigorous plumes, it does not depend on plate velocity. For more sluggish plumes, however, variations in the plume spreading behaviour at the base of the lithosphere result in a decrease in the onset time of SSCs with increasing plate velocity. In any case, SSC results in uplift of the isotherm 1573 K by up to 20 km relative to its initial equilibrium depth at the impact point.
ISSN: 0956-540X

hal-00856763
https://hal.archives-ouvertes.fr/hal-00856763
DOI : 10.1093/gji/ggt128

Éditeur(s) : HAL CCSD Elsevier
Résumé : International audience
Studies performed in the last decades have highlighted the need to better understand the contribution of the endothelium, vascular function, oxidative stress, inflammation, coagulation, hemolysis and vascular adhesion mechanisms to the pathophysiology of acute vaso-occlusive like events and chronic organ damages in sickle cell disease (SCD). Although SCD is a hemorheological disease, a few works focused on the contribution of blood viscosity, plasma viscosity, red blood cell deformability and aggregation in the pathophysiology of SCD. After a brief description of basic hemorheology, the present review focuses on the role of the hemorheological abnormalities in the causation of several SCD complications, mainly in sickle cell anemia and hemoglobin (Hb) SC disease. Several genetic and cellular modulators of blood rheology in SCD are discussed, as well as unresolved questions and perspectives.
ISSN: 0268-960X

hal-01668334
https://hal.univ-antilles.fr/hal-01668334
DOI : 10.1016/j.blre.2015.08.005

Éditeur(s) : HAL CCSD IOS Press
Résumé : International audience
The aim of the present study was to test the effects of hydroxyurea (HU) therapy on clinical, hematological and hemorheological parameters in adult patients with sickle cell anemia (SCA). Hematological and hemorheological parameters were measured in 28 SCA patients before HU therapy (i.e., baseline) and at 6, 12 and 24 months of treatment. RBC deformability was determined by ektacytometry at 30 Pa. RBC aggregation properties were investigated by light-backscatter method. Blood viscosity was measured at 225 s-1 by a cone-plate viscometer. The rates of vaso-occlusive crises and acute chest syndrome were lower at 1 and 2 years of HU therapy compared to baseline. The proportion of patients with leg ulcers tended to decrease after 2 years of treatment. Hemoglobin oxygen saturation improved with HU therapy. HU therapy induced a decrease of platelet and white blood cell counts and a rise in fetal hemoglobin level and mean cell volume. While hemoglobin concentrations increased under HU, blood viscosity remained unchanged all along the study. RBC deformability increased over baseline values at 6 months of HU therapy and continued to rise until the end of the follow-up period. In conclusion, the improvement in RBC deformability probably compensates the increase of hemoglobin on blood viscosity and participates to the improvement of the clinical status of patients.
ISSN: 1386-0291

hal-01668327
https://hal.univ-antilles.fr/hal-01668327
DOI : 10.3233/CH-170280