Mapping annual forest cover by fusing PALSAR/PALSAR-2 and MODIS NDVI during 2007–2016

Advanced Land Observing Satellite (ALOS) Phased Arrayed L-band Synthetic Aperture Radar (PALSAR) HH and HV polarization data were used previously to produce annual, global 25 m forest maps between 2007 and 2010, and the latest global forest maps of 2015 and 2016 were produced by using the ALOS-2 PALSAR-2 data. However, annual 25 m spatial resolution forest maps during 2011–2014 are missing because of the gap in operation between ALOS and ALOS-2, preventing the construction of a continuous, fine resolution time-series dataset on the world's forests. In contrast, the MODerate Resolution Imaging Spectroradiometer (MODIS) NDVI images were available globally since 2000. This research developed a novel method to produce annual 25 m forest maps during 2007–2016 by fusing the fine spatial resolution, but asynchronous PALSAR/PALSAR-2 with coarse spatial resolution, but synchronous MODIS NDVI data, thus, filling the four-year gap in the ALOS and ALOS-2 time-series, as well as enhancing the existing mapping activity. The method was developed concentrating on two key objectives: 1) producing more accurate 25 m forest maps by integrating PALSAR/PALSAR-2 and MODIS NDVI data during 2007–2010 and 2015–2016; 2) reconstructing annual 25 m forest maps from time-series MODIS NDVI images during 2011–2014. Specifically, a decision tree classification was developed for forest mapping based on both the PALSAR/PALSAR-2 and MODIS NDVI data, and a new spatial-temporal super-resolution mapping was proposed to reconstruct the 25 m forest maps from time-series MODIS NDVI images. Three study sites including Paraguay, the USA and Russia were chosen, as they represent the world's three main forest types: tropical forest, temperate broadleaf and mixed forest, and boreal conifer forest, respectively. Compared with traditional methods, the proposed approach produced the most accurate continuous time-series of fine spatial resolution forest maps both visually and quantitatively. For the forest maps during 2007–2010 and 2015–2016, the results had greater overall accuracy values (>98%) than those of the original JAXA forest product. For the reconstructed 25 m forest maps during 2011–2014, the increases in classifications accuracy relative to three benchmark methods were statistically significant, and the overall accuracy values of the three study sites were almost universally >92%. The proposed approach, therefore, has great potential to support the production of annual 25 m forest maps by fusing PALSAR/PALSAR-2 and MODIS NDVI during 2007–2016

Shoulder muscle activity in sport climbing in naturally chosen and corrected shoulder positions

Objective: The aim of the study was to determine electromyographic activity of the scapula stabilizing muscles in naturally chosen and corrected shoulder positions in typical static climbing postures. Methods: Six male participants undertook surface electromyography measurement in four climbing postures for two different shoulder positions. The activity of the lower, middle and upper trapezius, serratus anterior, pectoralis major, and sternocleidomastoid was recorded. Electromyographic activity was expressed as the percentage of maximal voluntary contraction (MVC) for each muscle. Results: Climbing postures induced higher activation of middle and lower trapezius in corrected shoulder positions (35.3 ± 11.8 and 61.7 ± 15.4% MVC respectively) than in naturally chosen shoulder positions (18.4 ± 8.9 and 30.1 ± 13.8% MVC respectively). The highest activity of the middle and lower trapezius was found in postures with the arm in external rotation and 90° abduction and in an overhanging posture. Low activation was stated for the other muscles in both shoulder conditions. Conclusion: Results showed that climbers naturally elevate the shoulder during typical static postures. Corrected shoulder positions induce higher activation of the scapula stabilizing muscles than naturally chosen shoulder positions.N/

Observation and Modeling of the Solar-Cycle Variation of the Meridional Flow

We present independent observations of the solar-cycle variation of flows near the solar surface and at a depth of about 60 Mm, in the latitude range $\pm45^\circ$. We show that the time-varying components of the meridional flow at these two depths have opposite sign, while the time-varying components of the zonal flow are in phase. This is in agreement with previous results. We then investigate whether the observations are consistent with a theoretical model of solar-cycle dependent meridional circulation based on a flux-transport dynamo combined with a geostrophic flow caused by increased radiative loss in the active region belt (the only existing quantitative model). We find that the model and the data are in qualitative agreement, although the amplitude of the solar-cycle variation of the meridional flow at 60 Mm is underestimated by the model.Comment: To be published in Solar Physcis Topical Issue "Helioseismology, Asteroseismology, and MHD Connections

Time--Distance Helioseismology Data Analysis Pipeline for Helioseismic and Magnetic Imager onboard Solar Dynamics Observatory (SDO/HMI) and Its Initial Results

The Helioseismic and Magnetic Imager onboard the Solar Dynamics Observatory (SDO/HMI) provides continuous full-disk observations of solar oscillations. We develop a data-analysis pipeline based on the time-distance helioseismology method to measure acoustic travel times using HMI Doppler-shift observations, and infer solar interior properties by inverting these measurements. The pipeline is used for routine production of near-real-time full-disk maps of subsurface wave-speed perturbations and horizontal flow velocities for depths ranging from 0 to 20 Mm, every eight hours. In addition, Carrington synoptic maps for the subsurface properties are made from these full-disk maps. The pipeline can also be used for selected target areas and time periods. We explain details of the pipeline organization and procedures, including processing of the HMI Doppler observations, measurements of the travel times, inversions, and constructions of the full-disk and synoptic maps. Some initial results from the pipeline, including full-disk flow maps, sunspot subsurface flow fields, and the interior rotation and meridional flow speeds, are presented.Comment: Accepted by Solar Physics topical issue 'Solar Dynamics Observatory

Measurement of the branching fraction for Υ(1S)→τ+τ−\Upsilon (1S) \to \tau^+ \tau^-

We have studied the leptonic decay of the $\Upsilon (1S)$ resonance into tau pairs using the CLEO II detector. A clean sample of tau pair events is identified via events containing two charged particles where exactly one of the particles is an identified electron. We find $B(\Upsilon(1S) \to \tau^+ \tau^-) = (2.61~\pm~0.12~{+0.09\atop{-0.13}})$. The result is consistent with expectations from lepton universality.Comment: 9 pages, RevTeX, two Postscript figures available upon request, CLNS 94/1297, CLEO 94-20 (submitted to Physics Letters B

Subsurface Meridional Circulation in the Active Belts

Temporal variations of the subsurface meridional flow with the solar cycle have been reported by several authors. The measurements are typically averaged over periods of time during which surface magnetic activity existed in the regions were the velocities are calculated. The present work examines the possible contamination of these measurements due to the extra velocity fields associated with active regions plus the uncertainties in the data obtained where strong magnetic fields are present. We perform a systematic analysis of more than five years of GONG data and compare meridional flows obtained by ring-diagram analysis before and after removing the areas of strong magnetic field. The overall trend of increased amplitude of the meridional flow towards solar minimum remains after removal of large areas associated with surface activity. We also find residual circulation toward the active belts that persist even after the removal of the surface magnetic activity, suggesting the existence of a global pattern or longitudinally-located organized flows.Comment: 12 pages, 6 figures, Submitted to Solar Physics. Accepted (08/25/2008

Methotrexate-related central neurotoxicity: clinical characteristics, risk factors and genome-wide association study in children treated for acute lymphoblastic leukemia

Symptomatic methotrexate-related central neurotoxicity (MTX neurotoxicity) is a severe toxicity experienced during acute lymphoblastic leukemia (ALL) therapy with potential long-term neurologic complications. Risk factors and long-term outcomes require further study. We conducted a systematic, retrospective review of 1,251 consecutive Australian children enrolled on Berlin-Frankfurt-Münster or Children's Oncology Group-based protocols between 1998-2013. Clinical risk predictors for MTX neurotoxicity were analyzed using regression. A genome-wide association study (GWAS) was performed on 48 cases and 537 controls. The incidence of MTX neurotoxicity was 7.6% (n=95 of 1,251), at a median of 4 months from ALL diagnosis and 8 days after intravenous or intrathecal MTX. Grade 3 elevation of serum aspartate aminotransferase (P=0.005, odds ratio 2.31 [range, 1.28–4.16]) in induction/consolidation was associated with MTX neurotoxicity, after accounting for the only established risk factor, age ≥10 years. Cumulative incidence of CNS relapse was increased in children where intrathecal MTX was omitted following symptomatic MTX neurotoxicity (n=48) compared to where intrathecal MTX was continued throughout therapy (n=1,174) (P=0.047). Five-year central nervous system relapse-free survival was 89.2±4.6% when intrathecal MTX was ceased compared to 95.4±0.6% when intrathecal MTX was continued. Recurrence of MTX neurotoxicity was low (12.9%) for patients whose intrathecal MTX was continued after their first episode. The GWAS identified single-nucletide polymorphism associated with MTX neurotoxicity near genes regulating neuronal growth, neuronal differentiation and cytoskeletal organization (P<1x10-6). In conclusion, increased serum aspartate aminotransferase and age ≥10 years at diagnosis were independent risk factors for MTX neurotoxicity. Our data do not support cessation of intrathecal MTX after a first MTX neurotoxicity event.Marion K. Mateos, Glenn M Marshall, Pasquale M. Barbaro, Michael C.J. Quinn, Carly George, Chelsea Mayoh, Rosemary Sutton, Tamas Revesz, Jodie E Giles, Draga Barbaric, Frank Alvaro, Françoise Mechinaud, Daniel Catchpoole, John A. Lawson, Georgia Chenevix-Trench, Stuart MacGregor, Rishi S.Kotecha, Luciano Dalla-Pozza, and Toby N. Traha

Genome-wide association meta-analysis of single-nucleotide polymorphisms and symptomatic venous thromboembolism during therapy for acute lymphoblastic leukemia and lymphoma in caucasian children

Symptomatic venous thromboembolism (VTE) occurs in five percent of children treated for acute lymphoblastic leukemia (ALL), but whether a genetic predisposition exists across different ALL treatment regimens has not been well studied.MethodsWe undertook a genome-wide association study (GWAS) meta-analysis for VTE in consecutively treated children in the Nordic/Baltic acute lymphoblastic leukemia 2008 (ALL2008) cohort and the Australian Evaluation of Risk of ALL Treatment-Related Side-Effects (ERASE) cohort. A total of 92 cases and 1481 controls of European ancestry were included.ResultsNo SNPs reached genome-wide significance (p -8) in either cohort. Among the top 34 single-nucleotide polymorphisms (SNPs) (p -6), two loci had concordant effects in both cohorts: ALOX15B (rs1804772) (MAF: 1%; p = 3.95 × 10-7) that influences arachidonic acid metabolism and thus platelet aggregation, and KALRN (rs570684) (MAF: 1%; p = 4.34 × 10-7) that has been previously associated with risk of ischemic stroke, atherosclerosis, and early-onset coronary artery disease.ConclusionThis represents the largest GWAS meta-analysis conducted to date associating SNPs to VTE in children and adolescents treated on childhood ALL protocols. Validation of these findings is needed and may then lead to patient stratification for VTE preventive interventions. As VTE hemostasis involves multiple pathways, a more powerful GWAS is needed to detect combination of variants associated with VTE.Marion K. Mateos, Morten Tulstrup, Michael CJ Quinn, Ruta Tuckuviene, Glenn M. Marshall, Ramneek Gupt

Hadronic contributions to (g−2)(g-2) of the leptons and to the effective fine structure constant α(MZ2)\alpha(M_Z^2)

The hadronic contributions to the anomalous magnetic moments of the leptons and to the effective fine structure constant at the Z-mass are reevaluated using all presently available $e^+ e^-$ data.Comment: 36 pages, 11 Postscript figures, available at ftp://129.129.40.58/pub/preprints/vapogm2.ps.g

Genetically Determined Height and Risk of Non-hodgkin Lymphoma

Although the evidence is not consistent, epidemiologic studies have suggested that taller adult height may be associated with an increased risk of some non-Hodgkin lymphoma (NHL) subtypes. Height is largely determined by genetic factors, but how these genetic factors may contribute to NHL risk is unknown. We investigated the relationship between genetic determinants of height and NHL risk using data from eight genome-wide association studies (GWAS) comprising 10,629 NHL cases, including 3,857 diffuse large B-cell lymphoma (DLBCL), 2,847 follicular lymphoma (FL), 3,100 chronic lymphocytic leukemia (CLL), and 825 marginal zone lymphoma (MZL) cases, and 9,505 controls of European ancestry. We evaluated genetically predicted height by constructing polygenic risk scores using 833 height-associated SNPs. We used logistic regression to estimate odds ratios (OR) and 95% confidence intervals (CI) for association between genetically determined height and the risk of four NHL subtypes in each GWAS and then used fixed-effect meta-analysis to combine subtype results across studies. We found suggestive evidence between taller genetically determined height and increased CLL risk (OR = 1.08, 95% CI = 1.00\u20131.17, p = 0.049), which was slightly stronger among women (OR = 1.15, 95% CI: 1.01\u20131.31, p = 0.036). No significant associations were observed with DLBCL, FL, or MZL. Our findings suggest that there may be some shared genetic factors between CLL and height, but other endogenous or environmental factors may underlie reported epidemiologic height associations with other subtypes