Three-dimensional seismic structure of the Mid-Atlantic Ridge : an investigation of tectonic, magmatic, and hydrothermal processes in the Rainbow Area

Author Posting. © American Geophysical Union, 2017. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research: Solid Earth 122 (2017): 9580–9602, doi:10.1002/2017JB015051.To test models of tectonic, magmatic, and hydrothermal processes along slow-spreading mid-ocean ridges, we analyzed seismic refraction data from the Mid-Atlantic Ridge INtegrated Experiments at Rainbow (MARINER) seismic and geophysical mapping experiment. Centered at the Rainbow area of the Mid-Atlantic Ridge (36°14'N), this study examines a section of ridge with volcanically active segments and a relatively amagmatic ridge offset that hosts the ultramafic Rainbow massif and its high-temperature hydrothermal vent field. Tomographic images of the crust and upper mantle show segment-scale variations in crustal structure, thickness, and the crust-mantle transition, which forms a vertical gradient rather than a sharp boundary. There is little definitive evidence for large regions of sustained high temperatures and melt in the lower crust or upper mantle along the ridge axes, suggesting that melts rising from the mantle intrude as small intermittent magma bodies at crustal and subcrustal levels. The images reveal large rotated crustal blocks, which extend to mantle depths in some places, corresponding to off-axis normal fault locations. Low velocities cap the Rainbow massif, suggesting an extensive near-surface alteration zone due to low-temperature fluid-rock reactions. Within the interior of the massif, seismic images suggest a mixture of peridotite and gabbroic intrusions, with little serpentinization. Here diffuse microearthquake activity indicates a brittle deformation regime supporting a broad network of cracks. Beneath the Rainbow hydrothermal vent field, fluid circulation is largely driven by the heat of small cooling melt bodies intruded into the base of the massif and channeled by the crack network and shallow faults.NSF Grant Numbers: OCE-0961151, OCE-09616802018-06-2

Magnetic phase diagram of antiferroquadrupole ordering in HoB2C2

The magnetic phase diagram for antiferro-quadrupole (AFQ) ordering in tetragonal HoB$_2$C$_2$ has been investigated by measurements of elastic constants $C_{11}$, $C_{44}$ and $C_{66}$ in fields along the basal $x$-$y$ plane as well as the principal [001]-axis. The hybrid magnet (GAMA) in Tsukuba Magnetic Laboratory was employed for high field measurements up to 30 T. The AFQ phase is no longer observed above 26.3 T along the principal [001] axis in contrast to the relatively small critical field of 3.9 T in fields applied along the basal [110] axis. The quadrupolar intersite interaction of $O_{xy}$ and/or $O_2^2$ is consistent with the anisotropy in the magnetic phase diagram of the AFQ phase in HoB$_2$C$_2$.Comment: Phys. Rev. B. (2005) in press. approx 8 pages, 10 figure

Imaging of membrane concentration polarization by NaCl using 23Na nuclear magnetic resonance

Forward osmosis (FO) and reverse osmosis (RO) membrane processes differ in their driving forces: osmotic pressure versus hydraulic pressure. Concentration polarization (CP) can adversely affect both performance and lifetime in such membrane systems. In order to mitigate against CP, the extent and severity of it need to be predicted more accurately through advanced online monitoring methodologies. Whilst a variety of monitoring techniques have been used to study the CP mechanism, there is still a pressing need to develop and apply non-invasive, in situ techniques able to produce quantitative, spatially resolved measurements of heterogeneous solute concentration in, and adjacent to, the membrane assembly as caused by the CP mechanism. To this end, 23Na magnetic resonance imaging (MRI) is used to image the sodium ion concentration within, and near to, both FO and RO composite membranes for the first time; this is also coupled with 1H MRI mapping of the corresponding water distribution. As such, it is possible to directly image salt accumulation due to CP processes during desalination. This was consistent with literature expectations and serves to confirm the suitability of 23Na MRI as a novel non-invasive technique for CP studies

An in vivo MRI Template Set for Morphometry, Tissue Segmentation, and fMRI Localization in Rats

Over the last decade, several papers have focused on the construction of highly detailed mouse high field magnetic resonance image (MRI) templates via non-linear registration to unbiased reference spaces, allowing for a variety of neuroimaging applications such as robust morphometric analyses. However, work in rats has only provided medium field MRI averages based on linear registration to biased spaces with the sole purpose of approximate functional MRI (fMRI) localization. This precludes any morphometric analysis in spite of the need of exploring in detail the neuroanatomical substrates of diseases in a recent advent of rat models. In this paper we present a new in vivo rat T2 MRI template set, comprising average images of both intensity and shape, obtained via non-linear registration. Also, unlike previous rat template sets, we include white and gray matter probabilistic segmentations, expanding its use to those applications demanding prior-based tissue segmentation, e.g., statistical parametric mapping (SPM) voxel-based morphometry. We also provide a preliminary digitalization of latest Paxinos and Watson atlas for anatomical and functional interpretations within the cerebral cortex. We confirmed that, like with previous templates, forepaw and hindpaw fMRI activations can be correctly localized in the expected atlas structure. To exemplify the use of our new MRI template set, were reported the volumes of brain tissues and cortical structures and probed their relationships with ontogenetic development. Other in vivo applications in the near future can be tensor-, deformation-, or voxel-based morphometry, morphological connectivity, and diffusion tensor-based anatomical connectivity. Our template set, freely available through the SPM extension website, could be an important tool for future longitudinal and/or functional extensive preclinical studies

Seismic imaging of magma sills beneath an ultramafic-hosted hydrothermal system

Author Posting. © The Author(s), 2017. This is the author's version of the work. It is posted here under a nonexclusive, irrevocable, paid-up, worldwide license granted to WHOI. It is made available for personal use, not for redistribution. The definitive version was published in Geology 45 (2017): 451-454, doi:10.1130/G38795.1.Hydrothermal circulation at mid-ocean ridge volcanic segments extracts heat from crustal magma bodies. However, the heat source driving hydrothermal circulation in ultramafic outcrops, where mantle rocks are exhumed in low-magma-supply environments, has remained enigmatic. Here we use a three-dimensional P-wave velocity model derived from active-source wide-angle refraction-reflection ocean bottom seismometer data and pre-stack depth-migrated images derived from multichannel seismic reflection data to investigate the internal structure of the Rainbow ultramafic massif, which is located in a non-transform discontinuity of the Mid-Atlantic Ridge. Seismic imaging reveals that the ultramafic rocks composing the Rainbow massif have been intruded by a large number of magmatic sills, distributed throughout the massif at depths of ∼2–10 km. These sills, which appear to be at varying stages of crystallization, can supply the heat needed to drive high-temperature hydrothermal circulation, and thus provide an explanation for the hydrothermal discharge observed in this ultramafic setting. Our results demonstrate that high-temperature hydrothermal systems can be driven by heat from deep-sourced magma even in exhumed ultramafic lithosphere with very low magma supply.This research was funded by National Science Foundation (NSF) grants OCE-0961680 and OCE-0961151

Comparison of gait event detection from shanks and feet in single-task and multi-task walking of healthy older adults

Automatic and objective detection algorithms for gait events from MEMS Inertial Measurement Units data have been developed to overcome subjective inaccuracy in traditional visual observation. Their accuracy and sensitivity have been verified with healthy older adults, Parkinson's disease and spinal injured patients, using single-task gait exercises, where events are precise as the subject is focusing only on walking. Multi-task walking instead simulates a more realistic and challenging scenario where subjects perform secondary cognitive task while walking, so it is a better benchmark. In this paper, we test two algorithms based on shank and foot angular velocity data in single-task, dual-task and multi-task walking. Results show that both algorithms fail when the subject slows extremely down or pauses due to high cognitive and attentional load, and, in particular, the first stride detection error rate of the foot-based algorithm increases. Stride time is accurate with both algorithms regardless of walking types, but the shank-based algorithm leads to an overestimation on the proportion of swing phase in one gait cycle. Increasing the number of cognitive tasks also causes this error with both algorithms

Squid adjust their body color according to substrate

Coleoid cephalopods camouflage on timescales of seconds to match their visual surroundings. To date, studies of cephalopod camouflage-to-substrate have been focused primarily on benthic cuttlefish and octopus, because they are readily found sitting on the substrate. In contrast to benthic cephalopods, oval squid (Sepioteuthis lessoniana species complex) are semi-pelagic animals that spend most of their time in the water column. In this study, we demonstrate that in captivity, S. lessoniana Sp.2 (Shiro-ika, white-squid) from the Okinawa archipelago, Japan, adapts the coloration of their skin using their chromatophores according to the background substrate. We show that if the animal moves between substrates of different reflectivity, the body patterning is changed to match. Chromatophore matching to substrate has not been reported in any loliginid cephalopod under laboratory conditions. Adaptation of the chromatophore system to the bottom substrate in the laboratory is a novel experimental finding that establishes oval squid as laboratory model animals for further research on camouflage

ISSAID/EMQN Best Practice Guidelines for the Genetic Diagnosis of Monogenic Autoinflammatory Diseases in the Next-Generation Sequencing Era

Abstract Background Monogenic autoinflammatory diseases are caused by pathogenic variants in genes that regulate innate immune responses, and are characterized by sterile systemic inflammatory episodes. Since symptoms can overlap within this rapidly expanding disease category, accurate genetic diagnosis is of the utmost importance to initiate early inflammation-targeted treatment and prevent clinically significant or life-threatening complications. Initial recommendations for the genetic diagnosis of autoinflammatory diseases were limited to a gene-by-gene diagnosis strategy based on the Sanger method, and restricted to the 4 prototypic recurrent fevers (MEFV, MVK, TNFRSF1A, and NLRP3 genes). The development of best practices guidelines integrating critical recent discoveries has become essential. Methods The preparatory steps included 2 online surveys and pathogenicity annotation of newly recommended genes. The current guidelines were drafted by European Molecular Genetics Quality Network members, then discussed by a panel of experts of the International Society for Systemic Autoinflammatory Diseases during a consensus meeting. Results In these guidelines, we combine the diagnostic strength of next-generation sequencing and recommendations to 4 more recently identified genes (ADA2, NOD2, PSTPIP1, and TNFAIP3), nonclassical pathogenic genetic alterations, and atypical phenotypes. We present a referral-based decision tree for test scope and method (Sanger versus next-generation sequencing) and recommend on complementary explorations for mosaicism, copy-number variants, and gene dose. A genotype table based on the 5-category variant pathogenicity classification provides the clinical significance of prototypic genotypes per gene and disease. Conclusions These guidelines will orient and assist geneticists and health practitioners in providing up-to-date and appropriate diagnosis to their patients

The My Active and Healthy Aging (My-AHA) ICT platform to detect and prevent frailty in older adults: Randomized control trial design and protocol

[EN] Introduction Frailty increases the risk of poor health outcomes, disability, hospitalization, and death in older adults and affects 7%¿12% of the aging population. Secondary impacts of frailty on psychological health and socialization are significant negative contributors to poor outcomes for frail older adults. Method The My Active and Healthy Aging (My-AHA) consortium has developed an information and communications technology¿based platform to support active and healthy aging through early detection of prefrailty and provision of individually tailored interventions, targeting multidomain risks for frailty across physical activity, cognitive activity, diet and nutrition, sleep, and psychosocial activities. Six hundred adults aged 60 years and older will be recruited to participate in a multinational, multisite 18-month randomized controlled trial to test the efficacy of the My-AHA platform to detect prefrailty and the efficacy of individually tailored interventions to prevent development of clinical frailty in this cohort. A total of 10 centers from Italy, Germany, Austria, Spain, United Kingdom, Belgium, Sweden, Japan, South Korea, and Australia will participate in the randomized controlled trial. Results Pilot testing (Alpha Wave) of the My-AHA platform and all ancillary systems has been completed with a small group of older adults in Europe with the full randomized controlled trial scheduled to commence in 2018. Discussion The My-AHA study will expand the understanding of antecedent risk factors for clinical frailty so as to deliver targeted interventions to adults with prefrailty. Through the use of an information and communications technology platform that can connect with multiple devices within the older adult's own home, the My-AHA platform is designed to measure an individual's risk factors for frailty across multiple domains and then deliver personalized domain-specific interventions to the individual. The My-AHA platform is technology-agnostic, enabling the integration of new devices and sensor platforms as they emerge.This project has received funding from the European Union's Horizon 2020 research and innovation program under grant agreement No 689582 and the Australian National Health and Medical Research Council (NHRMC) European Union grant scheme (1115818). M.J.S. reports personal fees from Eli Lilly (Australia) Pty Ltd and grants from Novotech Pty Ltd, outside the submitted work. All other authors report nothing to disclose.Summers, MJ.; Rainero, I.; Vercelli, AE.; Aumayr, GA.; De Rosario Martínez, H.; Mönter, M.; Kawashima, R. (2018). 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