Optimal Dredge Fleet Scheduling Within Environmental Work Windows

The U. S. Army Corps of Engineers oversees dredging in hundreds of navigation projects annually, through its fleet of government equipment and through individual contracts with private industry. The research presented here sought to examine the decision to allocate dredge resources to projects systemwide under necessary constraints. These constraints included environmental restrictions on when dredging could take place in response to the migration patterns of turtles, birds, fish, and other wildlife; dredge equipment resource availability; and varying equipment productivity rates that affected project completion times. The paper discusses problem definition and model formulation of optimal dredge fleet scheduling within environmental work windows. In addition, a sensitivity analysis was conducted to provide decision makers with quantitative insights into dredging program efficiency gains that could be realized systemwide if environmental restrictions were relaxed. Opportunities exist to provide decision makers with quantitative insights into how efficiencies might be obtained if targeted research were to show that particular restricted periods could be relaxed without adverse consequences to sensitive and endangered species

Development of a new SonovueTM contrast-enhanced ultrasound approach reveals temporal and age-related features of muscle microvascular responses to feeding

Compromised limb blood flow in aging may contribute to the development of sarcopenia, frailty, and the metabolic syndrome. We developed a novel contrast-enhanced ultrasound technique using Sonovue™ to characterize muscle microvasculature responses to an oral feeding stimulus (15 g essential amino acids) in young (~20 years) and older (~70 years) men. Intensity-time replenishment curves were made via an ultrasound probe “fixed” over the quadriceps, with intermittent high mechanical index destruction of microbubbles within muscle vasculature. This permitted real-time measures of microvascular blood volume (MBV), microvascular flow velocity (MFV) and their product, microvascular blood flow (MBF). Leg blood flow (LBF) was measured by Doppler and insulin by enzyme-linked immunosorbent assay. Steady-state contrast concentrations needed for comparison between different physiological states were achieved <150 sec from commencing Sonovue™ infusion, and MFV and MBV measurements were completed <120 sec thereafter. Interindividual coefficients of variation in MBV and MFV were 35–40%, (N = 36). Younger men (N = 6) exhibited biphasic vascular responses to feeding with early increases in MBV (+36%, P < 0.008 45 min post feed) reflecting capillary recruitment, and late increases in MFV (+77%, P < 0.008) and MBF (+130%, P < 0.007 195 min post feed) reflecting more proximal vessel dilatation. Early MBV responses were synchronized with peak insulin but not increased LBF, while later changes in MFV and MBF occurred with insulin at post absorptive values but alongside increased LBF. All circulatory responses were absent in old men (N = 7). Thus, impaired postprandial circulation could impact age-related declines in muscle glucose disposal, protein anabolism, and muscle mass

Synchronous deficits in cumulative muscle protein synthesis and ribosomal biogenesis underlie age-related anabolic resistance to exercise in humans

Ageing is associated with impaired hypertrophic responses to resistance exercise training (RET). Here we investigated the aetiology of ‘anabolic resistance’ in older humans. Twenty healthy male individuals, 10 younger (Y; 23 ± 1 years) and 10 older (O; 69 ± 3 years), performed 6 weeks unilateral RET (6 × 8 repetitions, 75% of one repetition maximum (1-RM), 3 times per week). After baseline bilateral vastus lateralis (VL) muscle biopsies, subjects consumed 150 ml D2O (70 atom%; thereafter 50 ml week−1), further bilateral VL muscle biopsies were taken at 3 and 6 weeks to quantify muscle protein synthesis (MPS) via gas chromatography–pyrolysis–isotope ratio mass spectrometry. After RET, 1-RM increased in Y (+35 ± 4%) and O (+25 ± 3%; P < 0.01), while MVC increased in Y (+21 ± 5%; P < 0.01) but not O (+6 ± 3%; not significant (NS)). In comparison to Y, O displayed blunted RET-induced increases in muscle thickness (at 3 and 6 weeks, respectively, Y: +8 ± 1% and +11 ± 2%, P < 0.01; O: +2.6 ± 1% and +3.5 ± 2%, NS). While ‘basal’ longer term MPS was identical between Y and O (∼1.35 ± 0.1% day−1), MPS increased in response to RET only in Y (3 weeks, Y: 1.61 ± 0.1% day−1; O: 1.49 ± 0.1% day−1). Consistent with this, O exhibited inferior ribosomal biogenesis (RNA:DNA ratio and c-MYC induction: Y: +4 ± 2 fold change; O: +1.9 ± 1 fold change), translational efficiency (S6K1 phosphorylation, Y: +10 ± 4 fold change; O: +4 ± 2 fold change) and anabolic hormone milieu (testosterone, Y: 367 ± 19; O: 274 ± 19 ng dl−1 (all P < 0.05). Anabolic resistance is thus multifactorial

Latitudinal and Longitudinal Adaptation of Switchgrass Populations

Switchgrass (Panicum virgatum L.) is a warmseason native grass, used for livestock feed, bioenergy, soil and wildlife conservation, and prairie restoration in a large portion of the USA. The objective of this research was to quantify the relative importance of latitude and longitude for adaptation and agronomic performance of a diverse group of switchgrass populations. Six populations, chosen to represent remnant prairie populations on two north–south transects, were evaluated for agronomic traits at 12 locations ranging from 36 to 47°N latitude and 88 to 101°W longitude. Although the population × location interactions accounted for only 10 to 31% of the variance among population means, many significant changes in ranking and adaptive responses were observed. Ground cover was greater for northern-origin populations evaluated in hardiness zones 3 and 4 and for southern-origin populations evaluated in hardiness zones 5 and 6. There were no adaptive responses related to longitude (ecoregion). Switchgrass populations for use in biomass production, conservation, or restoration should not be moved more than one hardiness zone north or south from their origin, but some can be moved east or west of their original ecoregion, if results from field tests support broad longitudinal adaptation

Human skeletal muscle is refractory to the anabolic effects of leucine during the postprandial muscle-full period in older men

Leucine modulates muscle protein synthesis (MPS), with potential to facilitate accrual/maintenance of muscle mass. Animal models suggest that leucine boluses shortly after meals may prolong MPS and delay onset of a “muscle-full” state. However, the effects of nutrient “top-ups” in humans, and particularly older adults where deficits exist, have not been explored. We determined the effects of a leucine top-up after essential amino acid (EAA) feeding on anabolic signaling, MPS, and muscle energy metabolism in older men. During 13C6-phenylalanine infusion, 16 men (∼70 years) consumed 15 g of EAA with (n=8, FED + LEU) or without (n=8, FED) 3 g of leucine top-up 90 min later. Repeated blood and muscle sampling permitted measurement of fasting and postprandial plasma EAA, insulin, anabolic signaling including mTOR complex 1 (mTORC1) substrates, cellular ATP and phosphorylocreatine, and MPS. Oral EAA achieved rapid insulinemia (12.5 iU·ml−1 25 min post-feed), essential aminoacidemia (3000 μM, 45–65 min post-feed), and activation of mTORC1 signaling. Leucine top-up prolonged plasma EAA (2800 μM, 135 min) and leucine availability (1050 μM, 135 min post-feed). Fasting FSRs of 0.046 and 0.056%·h-1 (FED and FED + LEU respectively) increased to 0.085 and 0.085%·h-1 90–180 min post-feed and returned to basal rates after 180 min in both groups. Phosphorylation of mTORC1 substrates returned to fasting levels 240 min post-feed in both groups. Feeding had limited effect on muscle elongation factor 2 (eEF2) phosphorylation. We demonstrate the refractoriness of muscle to nutrient-led anabolic stimulation in the postprandial period; thus, leucine supplements should be taken outside of meals, or with meals containing suboptimal protein in terms of either amount or EAA composition

CIRCE: Coordinated Ionospheric Reconstruction Cubesat Experiment

The Coordinated Ionospheric Reconstruction Cubesat Experiment (CIRCE) is a collaborative space mission between the UK Defence Science and Technology Laboratory (Dstl), and the US Naval Research Laboratory (NRL) in developing small satellite ionospheric physics capability. CIRCE will characterise space weather effects on a regional scale in the ionosphere/thermosphere system. Properly characterising the dynamic ionosphere is important for a wide range of both civil and defence applications such as GPS, communications, and sensing technology. Consisting of two near-identical 6U (2x3U) CubeSat buses, the CIRCE nanosatellites will fly in a lead-follow tandem configuration in co-planar near-polar orbits at 500km altitude. Provided by Blue Canyon Technologies (BCT), the two buses will use differential drag to achieve and maintain an in-track separation of between 250 and 500km, allowing short time-scale dynamics to be observed in-situ. These nanosatellites each carry a complement of 5 individual scientific instruments, contributed from academic, industrial, and government partners across the UK and US. Scheduled to launch in 2021 via the US Department of Defence Space Test Program, the two CIRCE satellites will provide observations to enable a greater understanding of the driving processes of geophysical phenomena in the ionosphere/thermosphere system, distributed across a wide range of latitudes, and altitudes, as the mission progresses

Lunar Surface Engineering Properties Experiment Definition

The objectives of the research under this contract are to define geological and engineering problems associated with lunar exploration that depend on the knowledge of the mechanical properties of soil and rock for solution and to perform critical evaluation of available information relating to the composition, structure, and engineering properties of lunar surface materials.Submitted to : National Aeronautics and Space Administration, George C. Marshall Space Flight Center. Contract Number NAS 8-21432. Control Number DCN l-8-28-00056(IF)By James K. Mitchell, Richard E. Goodman, William N. Houston, Paul A. WitherspoonLunar soil simulation / W. N. Houston, L. I. Narniq, and J. K. Mitchell -- Friction angle of lunar surface soils estimated from boulder tracks / H. J. Hovland and J. K. Mitchell -- Trafficability of the lunar surface / J. B. Thompson and J. K. Mitchell -- Chemical impregnation techniques as related to lunar engineering applications / T. s. Vinson and J. K. Mitchell -- Failure of a borehole in soil or rock under dilatometer loading and under borehole jack loading / T. K. Van and R. E. Goodman -- Appendix - Detailed description of model studies / K. Drozd, T. K. Van, and R. E. Goodman -- Studies on fluid conductivity of lunar surface materials / D. F. Katz, D. R. Willis, and P. A. Witherspoon.Second quarterly repor

Btla signaling in conventional and regulatory lymphocytes coordinately tempers humoral immunity in the intestinal mucosa

The Btla inhibitory receptor limits innate and adaptive immune responses, both preventing the development of autoimmune disease and restraining anti-viral and anti-tumor responses. It remains unclear how the functions of Btla in diverse lymphocytes contribute to immunoregulation. Here, we show that Btla inhibits activation of genes regulating metabolism and cytokine signaling, including Il6 and Hif1a, indicating a regulatory role in humoral immunity. Within mucosal Peyer\u27s patches, we find T-cell-expressed Btla-regulated Tfh cells, while Btla in T or B cells regulates GC B cell numbers. Treg-expressed Btla is required for cell-intrinsic Treg homeostasis that subsequently controls GC B cells. Loss of Btla in lymphocytes results in increased IgA bound to intestinal bacteria, correlating with altered microbial homeostasis and elevations in commensal and pathogenic bacteria. Together our studies provide important insights into how Btla functions as a checkpoint in diverse conventional and regulatory lymphocyte subsets to influence systemic immune responses