207 research outputs found

    Quantifying the slip rates, spatial distribution and evolution of active normal faults from geomorphic analysis: Field examples from an oblique-extensional graben, southern Turkey

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    Quantifying the extent to which geomorphic features can be used to extract tectonic signals is a key challenge in the Earth Sciences. Here we analyse the drainage patterns, geomorphic impact, and long profiles of bedrock rivers that drain across and around normal faults in a regionally significant oblique-extensional graben (Hatay Graben) in southern Turkey that has been mapped geologically, but for which there are poor constraints on the activity, slip rates and Plio-Pleistocene evolution of basin-bounding faults. We show that drainage in the Hatay Graben is strongly asymmetric, and by mapping the distribution of wind gaps, we are able to evaluate how the drainage network has evolved through time. By comparing the presence, size, and distribution of long profile convexities, we demonstrate that the northern margin of the graben is tectonically quiescent, whereas the southern margin is bounded by active faults. Our analysis suggests that rivers crossing these latter faults are undergoing a transient response to ongoing tectonic uplift, and this interpretation is supported by classic signals of transience such as gorge formation and hill slope rejuvenation within the convex reach. Additionally, we show that the height of long profile convexities varies systematically along the strike of the southern margin faults, and we argue that this effect is best explained if fault linkage has led to an increase in slip rate on the faults through time from ∼ 0.1 to 0.45 mm/yr. By measuring the average length of the original fault segments, we estimate the slip rate enhancement along the faults, and thus calculate the range of times for which fault acceleration could have occurred, given geological estimates of fault throw. These values are compared with the times and slip rates required to grow the documented long-profile convexities enabling us to quantify both the present-day slip rate on the fault (0.45 ± 0.05 mm/yr) and the timing of fault acceleration (1.4 ± 0.2 Ma). Our results have substantial implications for predicting earthquake hazard in this densely populated area (calculated potential Mw = 6.0-6.6), enable us to constrain the tectonic evolution of the graben through time, and more widely, demonstrate that geomorphic analysis can be used as an effective tool for estimating fault slip rates over time periods > 106 years, even in the absence of direct geodetic constraints. © 2008 Elsevier B.V. All rights reserved

    Geomorphic and geological constraints on the active normal faulting of the Gediz (AlaÅŸehir) Graben, Western Turkey.

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    The Gediz (Alaşehir) Graben is located in the highly tectonically active region of Western Turkey. Extension due to regional geodynamic controls has resulted in a broadly two-phase evolution of the graben; firstly, low-angle normal faulting relating to the exhumation of the Menderes Massif metamorphic core complex took place between 16 - 2.6 Ma. Secondly, high-angle normal faulting initiated ~ 2 Ma forming the Gediz and other E-W trending grabens in the region. Here we quantify the throw rate along the fault array over the last 2.6, 2 and 0.7 Ma using structural and geological constraints, along with analysis of topographic relief as a proxy for footwall uplift. We derive, for the first time, time averaged rates of fault motion from 0.4 mm/yr to 1.3 mm/yr along the strike of the Gediz Graben, with variation in throw-rate associated with the geometry of individual fault strands. Patterns in throw-rate along strike of the graben bounding fault array also suggest that the fault segments have become linked during the last 2.6 - 2 Ma, possibly at 0.8 – 0.7 Ma. Furthermore, these data suggest that an earthquake occurring along the graben bounding fault could have a maximum predicted Mw of 6.3 - 7.6

    Normal fault growth and linkage in the Gediz (Alasehir) Graben, Western Turkey, revealed by transient river long-profiles and slope-break knickpoints

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    The Gediz (Alaşehir) Graben is located in the highly tectonically active and seismogenic region of Western Turkey. The rivers upstream of the normal fault-bounded graben each contain a non-lithologic knickpoint, including those that drain through inferred fault segment boundaries. Knickpoint heights measured vertically from the fault scale with footwall relief and documented fault throw (vertical displacement). Consequently, we deduce these knickpoints were initiated by an increase in slip rate on the basin-bounding fault, driven by linkage of the three main fault segments of the high-angle graben bounding fault array. Fault interaction theory and ratios of channel steepness suggest that the slip rate enhancement factor on linkage was a factor of 3. We combine this information with geomorphic and structural constraints to estimate that linkage took place between 0.6 Ma and 1 Ma. Calculated pre- and post-linkage throw rates are 0.6 and 2 mm/yr respectively. Maximum knickpoint retreat rates upstream of the faults range from 4.5 to 28 mm/yr, faster than for similar catchments upstream of normal faults in the Central Apennines and the Hatay Graben of Turkey, and implying a fluvial landscape response time of 1.6 to 2.7 Myr. We explore the relative controls of drainage area and precipitation on these retreat rates, and conclude that while climate variation and fault throw rate partially explain the variations seen, lithology remains a potentially important but poorly characterised variable

    What has finite element analysis taught us about diabetic foot disease and its management?:a systematic review

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    Over the past two decades finite element (FE) analysis has become a popular tool for researchers seeking to simulate the biomechanics of the healthy and diabetic foot. The primary aims of these simulations have been to improve our understanding of the foot's complicated mechanical loading in health and disease and to inform interventions designed to prevent plantar ulceration, a major complication of diabetes. This article provides a systematic review and summary of the findings from FE analysis-based computational simulations of the diabetic foot.A systematic literature search was carried out and 31 relevant articles were identified covering three primary themes: methodological aspects relevant to modelling the diabetic foot; investigations of the pathomechanics of the diabetic foot; and simulation-based design of interventions to reduce ulceration risk.Methodological studies illustrated appropriate use of FE analysis for simulation of foot mechanics, incorporating nonlinear tissue mechanics, contact and rigid body movements. FE studies of pathomechanics have provided estimates of internal soft tissue stresses, and suggest that such stresses may often be considerably larger than those measured at the plantar surface and are proportionally greater in the diabetic foot compared to controls. FE analysis allowed evaluation of insole performance and development of new insole designs, footwear and corrective surgery to effectively provide intervention strategies. The technique also presents the opportunity to simulate the effect of changes associated with the diabetic foot on non-mechanical factors such as blood supply to local tissues.While significant advancement in diabetic foot research has been made possible by the use of FE analysis, translational utility of this powerful tool for routine clinical care at the patient level requires adoption of cost-effective (both in terms of labour and computation) and reliable approaches with clear clinical validity for decision making

    CDK targets Sae2 to control DNA-end resection and homologous recombination

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    DNA double-strand breaks (DSBs) are repaired by two principal mechanisms: non-homologous end-joining (NHEJ) and homologous recombination (HR)1. HR is the most accurate DSB repair mechanism but is generally restricted to the S and G2 phases of the cell cycle, when DNA has been replicated and a sister chromatid is available as a repair template2-5. By contrast, NHEJ operates throughout the cell cycle but assumes most importance in G1 (refs 4​, ​6). The choice between repair pathways is governed by cyclin-dependent protein kinases (CDKs)2,3,5,7, with a major site of control being at the level of DSB resection, an event that is necessary for HR but not NHEJ, and which takes place most effectively in S and G2 (refs 2​, ​5). Here we establish that cell-cycle control of DSB resection in Saccharomyces cerevisiae results from the phosphorylation by CDK of an evolutionarily conserved motif in the Sae2 protein. We show that mutating Ser 267 of Sae2 to a non-phosphorylatable residue causes phenotypes comparable to those of a sae2Δ null mutant, including hypersensitivity to camptothecin, defective sporulation, reduced hairpin-induced recombination, severely impaired DNA-end processing and faulty assembly and disassembly of HR factors. Furthermore, a Sae2 mutation that mimics constitutive Ser 267 phosphorylation complements these phenotypes and overcomes the necessity of CDK activity for DSB resection. The Sae2 mutations also cause cell-cycle-stage specific hypersensitivity to DNA damage and affect the balance between HR and NHEJ. These findings therefore provide a mechanistic basis for cell-cycle control of DSB repair and highlight the importance of regulating DSB resection

    Early warning signals of simulated Amazon rainforest dieback

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    Copyright © The Author(s) 2013. This article is published with open access at Springerlink.comWe test proposed generic tipping point early warning signals in a complex climate model (HadCM3) which simulates future dieback of the Amazon rainforest. The equation governing tree cover in the model suggests that zero and non-zero stable states of tree cover co-exist, and a transcritical bifurcation is approached as productivity declines. Forest dieback is a non-linear change in the non-zero tree cover state, as productivity declines, which should exhibit critical slowing down. We use an ensemble of versions of HadCM3 to test for the corresponding early warning signals. However, on approaching simulated Amazon dieback, expected early warning signals of critical slowing down are not seen in tree cover, vegetation carbon or net primary productivity. The lack of a convincing trend in autocorrelation appears to be a result of the system being forced rapidly and non-linearly. There is a robust rise in variance with time, but this can be explained by increases in inter-annual temperature and precipitation variability that force the forest. This failure of generic early warning indicators led us to seek more system-specific, observable indicators of changing forest stability in the model. The sensitivity of net ecosystem productivity to temperature anomalies (a negative correlation) generally increases as dieback approaches, which is attributable to a non-linear sensitivity of ecosystem respiration to temperature. As a result, the sensitivity of atmospheric CO2 anomalies to temperature anomalies (a positive correlation) increases as dieback approaches. This stability indicator has the benefit of being readily observable in the real world.NERCJoint DECC/Defra Met Office Hadley Centre Climate ProgrammeUniversity of Exete

    Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes

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    Mitochondrial DNA (mtDNA) deletions are a common cause of mitochondrial disorders. Large mtDNA deletions can lead to a broad spectrum of clinical features with different age of onset, ranging from mild mitochondrial myopathies (MM), progressive external ophthalmoplegia (PEO), and Kearns-Sayre syndrome (KSS), to severe Pearson syndrome. The aim of this study is to investigate the molecular signatures surrounding the deletion breakpoints and their association with the clinical phenotype and age at onset. MtDNA deletions in 67 patients were characterized using array comparative genomic hybridization (aCGH) followed by PCR-sequencing of the deletion junctions. Sequence homology including both perfect and imperfect short repeats flanking the deletion regions were analyzed and correlated with clinical features and patients' age group. In all age groups, there was a significant increase in sequence homology flanking the deletion compared to mtDNA background. The youngest patient group (<6 years old) showed a diffused pattern of deletion distribution in size and locations, with a significantly lower sequence homology flanking the deletion, and the highest percentage of deletion mutant heteroplasmy. The older age groups showed rather discrete pattern of deletions with 44% of all patients over 6 years old carrying the most common 5 kb mtDNA deletion, which was found mostly in muscle specimens (22/41). Only 15% (3/20) of the young patients (<6 years old) carry the 5 kb common deletion, which is usually present in blood rather than muscle. This group of patients predominantly (16 out of 17) exhibit multisystem disorder and/or Pearson syndrome, while older patients had predominantly neuromuscular manifestations including KSS, PEO, and MM. In conclusion, sequence homology at the deletion flanking regions is a consistent feature of mtDNA deletions. Decreased levels of sequence homology and increased levels of deletion mutant heteroplasmy appear to correlate with earlier onset and more severe disease with multisystem involvement

    Bias and heteroscedastic memory error in self-reported health behavior: an investigation using covariance structure analysis

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    BACKGROUND: Frequent use of self-reports for investigating recent and past behavior in medical research requires statistical techniques capable of analyzing complex sources of bias associated with this methodology. In particular, although decreasing accuracy of recalling more distant past events is commonplace, the bias due to differential in memory errors resulting from it has rarely been modeled statistically. METHODS: Covariance structure analysis was used to estimate the recall error of self-reported number of sexual partners for past periods of varying duration and its implication for the bias. RESULTS: Results indicated increasing levels of inaccuracy for reports about more distant past. Considerable positive bias was found for a small fraction of respondents who reported ten or more partners in the last year, last two years and last five years. This is consistent with the effect of heteroscedastic random error where the majority of partners had been acquired in the more distant past and therefore were recalled less accurately than the partners acquired more recently to the time of interviewing. CONCLUSIONS: Memory errors of this type depend on the salience of the events recalled and are likely to be present in many areas of health research based on self-reported behavior
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