Lag and mixing during sediment transfer across the Tian Shan piedmont caused by climate-driven aggradation-incision cycles

Transient sediment storage and mixing of deposits of various ages during transport across alluvial piedmonts alter the clastic sedimentary record. We quantify buffering and mixing during cycles of aggradation–incision in the north piedmont of the Eastern Tian Shan. We complement existing chronologic data with 20 new luminescence ages and one cosmogenic radionuclide age of terrace abandonment and alluvial aggradation. Over the last 0.5 Myr, the piedmont deeply incised and aggraded many times per 100 kyr. Aggradation is driven by an increased flux of glacial sediment accumulated in the high range and flushed onto the piedmont by greater water discharge at stadial–interstadial transitions. After this sediment is evacuated from the high range, the reduced input sediment flux results in fluvial incision of the piedmont as fast as 9 cm year−1 and to depths up to 330 m. The timing of incision onset is different in each river and does not directly reflect climate forcing but the necessary time for the evacuation of glacial sediment from the high range. A significant fraction of sediments evacuated from the high range is temporarily stored on the piedmont before a later incision phase delivers it to the basin. Coarse sediments arrive in the basin with a lag of at least 7–14 kyrs between the first evacuation from the mountain and later basinward transport. The modern output flux of coarse sediments from the piedmont contains a significant amount of recycled material that was deposited on the piedmont as early as the Middle Pleistocene. Variations in temperature and moisture delivered by the Westerlies are the likely cause of repeated aggradation–incision cycles in the north piedmont instead of monsoonal precipitation. The arrival of the gravel front into the proximal basin is delayed relative to the fine-grained load and both are separated by a hiatus. This work shows, based on field observations and data, how sedimentary systems respond to climatic perturbations, and how sediment recycling and mixing can ensue

Implicating Calpain in Tau-Mediated Toxicity In Vivo

Alzheimer's disease and other related neurodegenerative disorders known as tauopathies are characterized by the accumulation of abnormally phosphorylated and aggregated forms of the microtubule-associated protein tau. Several laboratories have identified a 17 kD proteolytic fragment of tau in degenerating neurons and in numerous cell culture models that is generated by calpain cleavage and speculated to contribute to tau toxicity. In the current study, we employed a Drosophila tauopathy model to investigate the importance of calpain-mediated tau proteolysis in contributing to tau neurotoxicity in an animal model of human neurodegenerative disease. We found that mutations that disrupted endogenous calpainA or calpainB activity in transgenic flies suppressed tau toxicity. Expression of a calpain-resistant form of tau in Drosophila revealed that mutating the putative calpain cleavage sites that produce the 17 kD fragment was sufficient to abrogate tau toxicity in vivo. Furthermore, we found significant toxicity in the fly retina associated with expression of only the 17 kD tau fragment. Collectively, our data implicate calpain-mediated proteolysis of tau as an important pathway mediating tau neurotoxicity in vivo

Predicting major bleeding in patients with noncardioembolic stroke on antiplatelets

Objective: To develop and externally validate a prediction model for major bleeding in patients with a TIA or ischemic stroke on antiplatelet agents. Methods: We combined individual patient data from 6 randomized clinical trials (CAPRIE, ESPS-2, MATCH, CHARISMA, ESPRIT, and PRoFESS) investigating antiplatelet therapy after TIA or ischemic stroke. Cox regression analyses stratified by trial were performed to study the association between predictors and major bleeding. A risk prediction model was derived and validated in the PERFORM trial. Performance was assessed with the c statistic and calibration plots. Results: Major bleeding occurred in 1,530 of the 43,112 patients during 94,833 person-years of follow-up. The observed 3-year risk of major bleeding was 4.6% (95% confidence interval [CI] 4.4%–4.9%). Predictors were male sex, smoking, type of antiplatelet agents (aspirin-clopidogrel), outcome on modified Rankin Scale ≥3, prior stroke, high blood pressure, lower body mass index, elderly, Asian ethnicity, and diabetes (S2TOP-BLEED). The S2TOP-BLEED score had a c statistic of 0.63 (95% CI 0.60–0.64) and showed good calibration in the development data. Major bleeding risk ranged from 2% in patients aged 45–54 years without additional risk factors to more than 10% in patients aged 75–84 years with multiple risk factors. In external validation, the model had a c statistic of 0.61 (95% CI 0.59–0.63) and slightly underestimated major bleeding risk. Conclusions: The S2TOP-BLEED score can be used to estimate 3-year major bleeding risk in patients with a TIA or ischemic stroke who use antiplatelet agents, based on readily available characteristics. The discriminatory performance may be improved by identifying stronger predictors of major bleeding

Uncoupling neuronal death and dysfunction in Drosophila models of neurodegenerative disease

Common neurodegenerative proteinopathies, such as Alzheimer’s disease (AD) and Parkinson’s disease (PD), are characterized by the misfolding and aggregation of toxic protein species, including the amyloid beta (Aß) peptide, microtubule-associated protein Tau (Tau), and alpha-synuclein (αSyn) protein. These factors also show toxicity in Drosophila; however, potential limitations of prior studies include poor discrimination between effects on the adult versus developing nervous system and neuronal versus glial cell types. In addition, variable expression paradigms and outcomes hinder systematic comparison of toxicity profiles. Using standardized conditions and medium-throughput assays, we express human Tau, Aß or αSyn selectively in neurons of the adult Drosophila retina and monitor age-dependent changes in both structure and function, based on tissue histology and recordings of the electroretinogram (ERG), respectively. We find that each protein causes a unique profile of neurodegenerative pathology, demonstrating distinct and separable impacts on neuronal death and dysfunction. Strikingly, expression of Tau leads to progressive loss of ERG responses whereas retinal architecture and neuronal numbers are largely preserved. By contrast, Aß induces modest, age-dependent neuronal loss without degrading the retinal ERG. αSyn expression, using a codon-optimized transgene, is characterized by marked retinal vacuolar change, progressive photoreceptor cell death, and delayed-onset but modest ERG changes. Lastly, to address potential mechanisms, we perform transmission electron microscopy (TEM) to reveal potential degenerative changes at the ultrastructural level. Surprisingly, Tau and αSyn each cause prominent but distinct synaptotoxic profiles, including disorganization or enlargement of photoreceptor terminals, respectively. Our findings highlight variable and dynamic properties of neurodegeneration triggered by these disease-relevant proteins in vivo, and suggest that Drosophila may be useful for revealing determinants of neuronal dysfunction that precede cell loss, including synaptic changes, in the adult nervous system

[Postural balance following stroke: towards a disadvantage of the right brain-damaged hemisphere].

International audienceIn the light of studies published in the last ten years, we have suspected a differential influence of the sides of hemispheric cerebral lesions on posture and balance. A study was aimed at verifying this hypothesis, the method of which being original because many possible confounding factors such as age, sex as well as topography and size of the brain lesion have been taken into account in the statistical analysis. Inclusion criteria were: right-handed patients, first stroke, no previous disease which might have affected balance. Their postural abilities (ranging from 0 to 36) were assessed 90 +/- 3 days after stroke onset on a clinical scale. This clinical assessment was used here because it could be easily performed in all patients, irrespective of the severity of their impairment. Lesion locations were determined using the Atlas by Talairach and Tournoux and the number of cerebral areas altered gave an estimation of the lesion size. The first fifty patients consecutively admitted to rehabilitation and responding to the inclusion criteria were thus examined (25 with a right and 25 with a left hemispheric lesion; 14 women and 36 men; mean age 57.2 = yrs). The main result was lower postural performances in right brain-damaged patients than in left brain damaged patients (21.5 vs 29.4; p = 0.01). Postural abilities were also inversely related to age (r = -0.28; p = 0.04), lesion size (r = -0.41; p = 0.003) and were lower in women than in men (22.1 vs 28.8; p = 0.02). This study therefore confirms the existence of a right hemispheric dominance for postural control. The existence of inverse correlation between postural abilities and the number of omitted targets in cancellation task on one hand (r = -0.63, p < 0.001), the ipsilesional bias in line bissection on the other hand (r = -0.36; p = 0.01), argued for a relationship between the main result of this study and the well known cerebral organization of spatial information processing, based on a right hemisphere dominance for spatial attention and/or representation. The 'postural neglect' concept is discussed

Revisiting the andean tropical glacier behavior during the Antarctic cold reversal

International audienc