1,016 research outputs found

    The 2016 Southeastern U.S. Drought: An Extreme Departure From Centennial Wetting and Cooling

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    The fall 2016 drought in the southeastern United States (SE U.S.) appeared exceptional based on its widespread impacts, but the current monitoring framework that only extends from 1979 to present does not readily facilitate evaluation of soil-moisture anomalies in a centennial context. A new method to extend monthly gridded soil-moisture estimates back to 1895 is developed, indicating that since 1895, October–November 2016 soil moisture (0–200 cm) in the SE U.S. was likely the second lowest on record, behind 1954. This severe drought developed rapidly and was brought on by low September–November precipitation and record-high September–November daily maximum temperatures (Tmax). Record-high Tmax drove record-high atmospheric moisture demand, accounting for 28% of the October–November 2016 soil-moisture anomaly. Drought and heat in fall 2016 contrasted with 20th century wetting and cooling in the region but resembled conditions more common from 1895–1956. Dynamically, the exceptional drying in fall 2016 was driven by anomalous ridging over the central United States that reduced south-southwesterly moisture transports into the SE U.S. by approximately 75%. These circulation anomalies were partly promoted by a moderate La Niña and warmth in the tropical Atlantic, but these processes accounted for very little of the SE U.S. drying in fall 2016, implying a large role for internal atmospheric variability. The extended analysis back to 1895 indicates that SE U.S. droughts as strong as the 2016 event are more likely than indicated from a shorter 60 year perspective and continued multidecadal swings in precipitation may combine with future warming to further enhance the likelihood of such events

    Strip‐Bark Morphology and Radial Growth Trends in Ancient Pinus sibirica Trees From Central Mongolia

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    Some of the oldest and most important trees used for dendroclimatic reconstructions develop strip‐bark morphology, in which only a portion of the stem contains living tissue. Yet the ecophysiological factors initiating strip bark and the potential effect of cambial dieback on annual ring widths and tree‐ring estimates of past climate remain poorly understood. Using a combination of field observations and tree‐ring data, we investigate the causes and timing of cambial dieback events in Pinus sibirica strip‐bark trees from central Mongolia and compare the radial growth rates and trends of strip‐bark and whole‐bark trees over the past 515 years. Results indicate that strip bark is more common on the southern aspect of trees, and dieback events were most prevalent in the 19th century, a cold and dry period. Further, strip‐bark and whole‐bark trees have differing centennial trends, with strip‐bark trees exhibiting notably large increases in ring widths at the beginning of the 20th century. We find a steeper positive trend in the strip‐bark chronology relative to the whole‐bark chronology when standardizing with age‐dependent splines. We hypothesize that localized warming on the southern side of stems due to solar irradiance results in physiological damage and dieback and leads to increasing tree‐ring increment along the living portion of strip‐bark trees. Because the impact of cambial dieback on ring widths likely varies depending on species and site, we suggest conducting a comparison of strip‐bark and whole‐bark ring widths before statistically treating ring‐width data for climate reconstructions

    Comparing a Novel Neuroanimation Experience to Conventional Therapy for High-Dose Intensive Upper-Limb Training in Subacute Stroke: The SMARTS2 Randomized Trial

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    BACKGROUND Evidence from animal studies suggests that greater reductions in poststroke motor impairment can be attained with significantly higher doses and intensities of therapy focused on movement quality. These studies also indicate a dose-timing interaction, with more pronounced effects if high-intensity therapy is delivered in the acute/subacute, rather than chronic, poststroke period. OBJECTIVE To compare 2 approaches of delivering high-intensity, high-dose upper-limb therapy in patients with subacute stroke: a novel exploratory neuroanimation therapy (NAT) and modified conventional occupational therapy (COT). METHODS A total of 24 patients were randomized to NAT or COT and underwent 30 sessions of 60 minutes time-on-task in addition to standard care. The primary outcome was the Fugl-Meyer Upper Extremity motor score (FM-UE). Secondary outcomes included Action Research Arm Test (ARAT), grip strength, Stroke Impact Scale hand domain, and upper-limb kinematics. Outcomes were assessed at baseline, and days 3, 90, and 180 posttraining. Both groups were compared to a matched historical cohort (HC), which received only 30 minutes of upper-limb therapy per day. RESULTS There were no significant between-group differences in FM-UE change or any of the secondary outcomes at any timepoint. Both high-dose groups showed greater recovery on the ARAT (7.3 ± 2.9 points; P = .011) but not the FM-UE (1.4 ± 2.6 points; P = .564) when compared with the HC. CONCLUSIONS Neuroanimation may offer a new, enjoyable, efficient, and scalable way to deliver high-dose and intensive upper-limb therapy

    SARS-CoV-2 omicron BA.5 and XBB variants have increased neurotropic potential over BA.1 in K18-hACE2 mice and human brain organoids

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    The reduced pathogenicity of the omicron BA.1 sub-lineage compared to earlier variants is well described, although whether such attenuation is retained for later variants like BA.5 and XBB remains controversial. We show that BA.5 and XBB isolates were significantly more pathogenic in K18-hACE2 mice than a BA.1 isolate, showing increased neurotropic potential, resulting in fulminant brain infection and mortality, similar to that seen for original ancestral isolates. BA.5 also infected human cortical brain organoids to a greater extent than the BA.1 and original ancestral isolates. In the brains of mice, neurons were the main target of infection, and in human organoids neuronal progenitor cells and immature neurons were infected. The results herein suggest that evolving omicron variants may have increasing neurotropic potential
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