101 research outputs found

    Investigating ultra-low velocity zones in the southern hemisphere using an Antarctic dataset

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    Given limited seismic coverage of the lowermost mantle, less than one-fifth of the core-mantle boundary (CMB) has been surveyed for the presence of ultra-low velocity zones (ULVZs). Investigations that sample the CMB with new geometries are therefore important to further our understanding of ULVZ origins and their potential connection to other deep Earth processes. Using core-reflected ScP waves recorded by the recently deployed Transantarctic Mountains Northern Network in Antarctica, the current study aims to expand ULVZ investigations in the southern hemisphere. Our dataset samples the CMB in the vicinity of New Zealand, providing coverage between an area to the northeast, where ULVZ structure has been previously identified, and another region to the south, where prior evidence for a ULVZ was inconclusive. This area is of particular interest because the data sample across the boundary of the Pacific Large Low Shear Velocity Province (LLSVP). The Weddell Sea region near Antarctica is also well sampled, providing new information on a region that has not been previously studied. A correlative scheme between a large database of 1-D synthetic seismograms and the observed ScP data demonstrates that ULVZs are required in both study regions. Modeling uncertainties limit our ability to definitively define ULVZ characteristics but also likely indicate more complex 3-D structure. Given that ULVZs are detected within, along the edge of, and far from the Pacific LLSVP, our results support the hypothesis that ULVZs are compositionally distinct from the surrounding mantle and are not solely related to partial melt. ULVZs may be ubiquitous along the CMB; however, they may be thinner in many regions than can be resolved by current methods. Mantle convection currents may sweep the ULVZs into thicker piles in some areas, pushing these anomalies toward the boundaries of LLSVPs

    Dynamical links between small- and large-scale mantle heterogeneity: seismological evidence

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    We identify PKP*PKP scattered waves (also known as Pā€²*Pā€²) from earthquakes recorded at small-aperture seismic arrays at distances less than 65Ā°. Pā€²*Pā€² energy travels as a PKP wave through the core, up into the mantle, then scatters back down through the core to the receiver as a second PKP. Pā€²*Pā€² waves are unique in that they allow scattering heterogeneities throughout the mantle to be imaged. We use array processing methods to amplify low amplitude, coherent scattered energy signals and resolve their incoming direction. We deterministically map scattering heterogeneity locations from the core-mantle boundary to the surface. We use an extensive dataset with sensitivity to a large volume of the mantle and a location method allowing us to resolve and map more heterogeneities than have previously been possible, representing a significant increase in our understanding of small scale structure within the mantle. Our results demonstrate that the distribution of scattering heterogeneities varies both radially and laterally. Scattering is most abundant in the uppermost and lowermost mantle, and a minimum in the mid mantle, resembling the radial distribution of tomographically derived whole-mantle velocity heterogeneity. We investigate the spatial correlation of scattering heterogeneities with large-scale tomographic velocities, lateral velocity gradients, the locations of deep-seated hotspots and subducted slabs. In the lowermost 1500 km of the mantle, small-scale heterogeneities correlate with regions of low seismic velocity, high lateral seismic gradient, and proximity to hotspots. In the upper 1000 km of the mantle there is no significant correlation between scattering heterogeneity location and subducted slabs. Between 600 and 900 km depth, scattering heterogeneities are more common in the regions most remote from slabs, and close to hotspots. Scattering heterogeneities show an affinity for regions close to slabs within the upper 200 km of the mantle. The similarity between the distribution of large-scale and small-scale mantle structures suggests a dynamic connection across scales, whereby mantle heterogeneities of all sizes may be directed in similar ways by large-scale convective currents

    Seismic evidence for Earthā€™s crusty deep mantle

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    Seismic tomography resolves anomalies interpreted as oceanic lithosphere subducted deep into Earthā€™s lower mantle. However, the fate of the compositionally distinct oceanic crust that is part of the lithosphere is poorly constrained but provides important constraints on mixing processes and the recycling process in the deep Earth. We present high-resolution seismic array analyses of anomalous P-waves sampling the deep mantle, and deterministically locate heterogeneities in the lowermost 300 km of the mantle. Spectral analysis indicates that the dominant scale length of the heterogeneity is 4 to 7 km. The heterogeneity distribution varies laterally and radially and heterogeneities are more abundant near the margins of the lowermost mantle Large Low Velocity Provinces (LLVPs), consistent with mantle convection simulations that show elevated accumulations of deeply advected crustal material near the boundaries of thermo-chemical piles. The size and distribution of the observed heterogeneities is consistent with that expected for subducted oceanic crust. These results thus suggest the deep mantle contains an imprint of continued subduction of oceanic crust, stirred by mantle convection and modulated by long lasting thermo-chemical structures. The preferred location of the heterogeneity in the lowermost mantle is consistent with a thermo-chemical origin of the LLVPs. Our observations relate to the mixing behaviour of small length-scale heterogeneity in the deep Earth and indicate that compositional heterogeneities from the subduction process can survive for extended times in the lowermost mantle

    Š”учŠ°ŃŠ½ŠøŠ¹ стŠ°Š½ і ŠæрŠ¾Š±Š»ŠµŠ¼Šø уŠæрŠ°Š²Š»Ń–Š½Š½Ń Š·Š°Š»Ń–Š·Š½ŠøчŠ½ŠøŠ¼ трŠ°Š½ŃŠæŠ¾Ń€Ń‚Š¾Š¼ Š£ŠŗрŠ°Ń—Š½Šø

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    ŠŸŃ€Š¾Š°Š½Š°Š»Ń–Š·Š¾Š²Š°Š½Š¾ стŠ°Š½ і тŠµŠ½Š“ŠµŠ½Ń†Ń–Ń— рŠ¾Š·Š²ŠøтŠŗу Š·Š°Š»Ń–Š·Š½ŠøчŠ½Š¾Š³Š¾ трŠ°Š½ŃŠæŠ¾Ń€Ń‚Ńƒ. Š Š¾Š·Š³Š»ŃŠ½ŃƒŃ‚Ń– Š¾ŃŠ½Š¾Š²Š½Ń– Š·Š°Š²Š“Š°Š½Š½Ń Š“ŠµŃ€Š¶Š°Š²Š½Š¾Š³Š¾ рŠµŠ³ŃƒŠ»ŃŽŠ²Š°Š½Š½Ń Š³Š°Š»ŃƒŠ·Ń–.ŠŸŃ€Š¾Š°Š½Š°Š»ŠøŠ·ŠøрŠ¾Š²Š°Š½Š¾ сŠ¾ŃŃ‚Š¾ŃŠ½ŠøŠµ Šø тŠµŠ½Š“ŠµŠ½Ń†ŠøŠø рŠ°Š·Š²ŠøтŠøя Š¶ŠµŠ»ŠµŠ·Š½Š¾Š“Š¾Ń€Š¾Š¶Š½Š¾Š³Š¾ трŠ°Š½ŃŠæŠ¾Ń€Ń‚Š°. Š Š°ŃŃŠ¼Š¾Ń‚Ń€ŠµŠ½Š½Ń‹ Š¾ŃŠ½Š¾Š²Š½Ń‹Šµ Š·Š°Š“Š°Š½Šøя Š³Š¾ŃŃƒŠ“Š°Ń€ŃŃ‚Š²ŠµŠ½Š½Š¾Š³Š¾ рŠµŠ³ŃƒŠ»ŠøрŠ¾Š²Š°Š½Šøя Š¾Ń‚Ń€Š°ŃŠ»Šø.The condition and trends of railway transport has been anilized. The main tasks of state regulation of railway transport has been considereted

    Clinical Significance of Cartilage Biomarkers for Monitoring Structural Joint Damage in Rheumatoid Arthritis Patients Treated with Anti-TNF Therapy

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    PURPOSE: With the current use of biologics in rheumatoid arthritis (RA), there is a need to monitor ongoing structural joint damage due to the dissociation of articular cartilage damage from disease activity of RA. This study longitudinally analyzed levels of serum cartilage biomarkers during 54 weeks of infliximab therapy, to evaluate the feasibility of biomarkers for monitoring structural joint damage. METHODS: Subjects comprised 33 patients with early RA and 33 patients with established RA. All patients received 3 mg/kg of infliximab and methotrexate for 54 weeks. Levels of the following serum cartilage markers were measured at baseline and at weeks 14, 22, and 54: hyaluronan (HA); cartilage oligometric matrix protein (COMP); type II collagen (CII)-related neoepitope (C2C); type II procollagen carboxy-propeptide (CPII); and keratin sulfate (KS). Time courses for each biomarker were assessed, and relationships between these biomarkers and clinical or radiographic parameters generally used for RA were investigated. RESULTS: Levels of CRP, MMP-3, DAS28-CRP, and annual progression of TSS were improved to similar degrees in both groups at week 54. HA and C2C/CPII were significantly decreased compared to baseline in the early RA group (p<0.001), whereas HA and COMP, but not C2C/CPII, were decreased in the established RA group. Strikingly, serum C2C/CPII levels were universally improved in early RA, regardless of EULAR response grade. Both Ī”HA and Ī”C2C/CPII from baseline to week 54 correlated significantly with not only Ī”CRP, but also Ī”DAS28 in early RA. Interestingly, when partial correlation coefficients were calculated by standardizing CRP levels, the significant correlation of Ī”HA to Ī”DAS28 disappeared, whereas correlations of Ī”C2C/CPII to Ī”DAS28, Ī”JNS, and Ī”HAQ remained significant. These results suggest a role of Ī”C2C/CPII as a marker of ongoing structural joint damage with the least association with CRP, and that irreversible cartilage damage in established RA limits restoration of the C2C/CPII level, even with tight control of joint inflammation. CONCLUSION: The temporal course of C2C/CPII level during anti-TNF therapy indicates that CII turnover shifts toward CII synthesis in early RA, but not in established RA, potentially due to irreversible cartilage damage. Ī”C2C/CPII appears to offer a useful marker reflecting ongoing structural joint damage, dissociated from inflammatory indices such as CRP and MMP-3

    Circulating levels of dickkopf-1, osteoprotegerin and sclerostin are higher in old compared with young men and women and positively associated with whole-body bone mineral density in older adults

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    Summary: Bone mineral density declines with increasing older age. We examined the levels of circulating factors known to regulate bone metabolism in healthy young and older adults. The circulating levels of dickkopf-1, osteocalcin, osteoprotegerin and sclerostin were positively associated with WBMD in older adults, despite the average WBMD being lower and circulating dickkopf-1, osteoprotegerin and sclerostin being higher in old than young. Purpose: To investigate the relationship between whole-body bone mineral density (WBMD) and levels of circulating factors with known roles in bone remodelling during 'healthy' ageing. Methods: WBMD and fasting plasma concentrations of dickkopf-1, fibroblast growth factor-23, osteocalcin, osteoprotegerin, osteopontin and sclerostin were measured in 272 older subjects (69 to 81 years; 52% female) and 171 younger subjects (18-30 years; 53% female). Results: WBMD was lower in old than young. Circulating osteocalcin was lower in old compared with young, while dickkopf-1, osteoprotegerin and sclerostin were higher in old compared with young. These circulating factors were each positively associated with WBMD in the older adults and the relationships remained after adjustment for covariates (r-values ranging from 0.174 to 0.254, all p<0.01). In multivariate regression, the body mass index, circulating sclerostin and whole-body lean mass together accounted for 13.8% of the variation with WBMD in the older adults. In young adults, dickkopf-1 and body mass index together accounted for 7.7% of variation in WBMD. Conclusion: Circulating levels of dickkopf-1, osteocalcin, osteoprotegerin and sclerostin are positively associated with WBMD in community-dwelling older adults, despite the average WBMD being lower and circulating dickkopf-1, osteoprotegerin and sclerostin being higher in old than young

    Metabolic control and bone health in adolescents with type 1 diabetes

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    <p>Abstract</p> <p>Background</p> <p>Adults with type 1 diabetes (T1D) have decreased bone mineral density (BMD) and increased fracture risk, yet the etiologies remain elusive. Early detection of derangements in bone biomarkers during adolescence could lead to timely recognition. In adolescents with T1D, we evaluated the relationships between metabolic control, BMD, and bone anabolic and turnover markers.</p> <p>Methods</p> <p>Cross-sectional study of 57 adolescent subjects with T1D who had HbA1c consistently ā‰„ 9% (Poor Control, PC n = 27) or < 9% (Favorable Control, FC n = 30) for two years prior to enrollment. Subjects had T1DM for at least three years and were without diabetes complications, known celiac disease, or other chronic diseases.</p> <p>Results</p> <p>There were no differences between HbA1c groups in BMD, components of the IGF system, or 25-hydroxyvitamin D status. The prevalence of 25-hydroxyvitamin D abnormalities was similar to that seen in the general adolescent population. Few patients met the recommended dietary allowance (RDA) for vitamin D or calcium.</p> <p>Conclusions</p> <p>These data provide no evidence of association between degree of metabolic control and BMD in adolescents with T1D. Adolescents with T1D have a high prevalence of serum 25-hydroxyvitamin D abnormalities. Longitudinal studies are needed to evaluate the predictive value of vitamin D abnormalities on fracture risk.</p

    Inflammatory Rheumatic Disorders and Bone

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    Inflammatory joint diseases such as rheumatoid arthritis, as well as other rheumatic conditions, such as systemic lupus erythematosus (SLE) and ankylosing spondylitis, comprise a heterogeneous group of joint disorders that are all associated with extra-articular side effects, including bone loss and fractures. The concept of osteoimmunology is based on growing insights into the links between the immune system and bone. The pathogenesis of osteoporosis in these patients is multifactorial. We have, more or less as an example, described this extensively for patients with SLE. High disease activity (inflammation) and immobility are common factors that substantially increase fracture risk in these patients, on top of the background fracture risk based on, among other factors, age, body mass index, and gender. Although no fracture reduction has been shown in intervention studies in patients with inflammatory rheumatic diseases, we present treatment options that might be useful for clinicians who are treating these patients

    An increase in dietary n-3 fatty acids decreases a marker of bone resorption in humans

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    Human, animal, and in vitro research indicates a beneficial effect of appropriate amounts of omega-3 (n-3) polyunsaturated fatty acids (PUFA) on bone health. This is the first controlled feeding study in humans to evaluate the effect of dietary plant-derived n-3 PUFA on bone turnover, assessed by serum concentrations of N-telopeptides (NTx) and bone-specific alkaline phosphatase (BSAP). Subjects (n = 23) consumed each diet for 6 weeks in a randomized, 3-period crossover design: 1) Average American Diet (AAD; [34% total fat, 13% saturated fatty acids (SFA), 13% monounsaturated fatty acids (MUFA), 9% PUFA (7.7% LA, 0.8% ALA)]), 2) Linoleic Acid Diet (LA; [37% total fat, 9% SFA, 12% MUFA, 16% PUFA (12.6% LA, 3.6% ALA)]), and 3) Ī±-Linolenic Acid Diet (ALA; [38% total fat, 8% SFA, 12% MUFA, 17% PUFA (10.5% LA, 6.5% ALA)]). Walnuts and flaxseed oil were the predominant sources of ALA. NTx levels were significantly lower following the ALA diet (13.20 Ā± 1.21 nM BCE), relative to the AAD (15.59 Ā± 1.21 nM BCE) (p < 0.05). Mean NTx level following the LA diet was 13.80 Ā± 1.21 nM BCE. There was no change in levels of BSAP across the three diets. Concentrations of NTx were positively correlated with the pro-inflammatory cytokine TNFĪ± for all three diets. The results indicate that plant sources of dietary n-3 PUFA may have a protective effect on bone metabolism via a decrease in bone resorption in the presence of consistent levels of bone formation
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