Image enhancement software for underwater recovery operations - user's manual

This report describes software for performing image enhancement on live or recorded video images. The software was developed for operational use during underwater recovery operations at the Naval Undersea Warfare Engineering Station. The image processing is performed on an IBM-PC/AT compatible computer equipped with hardware to digitize and display video images. The software provides the capability to provide contrast enhancement and other similar functions in real time through hardware lookup tables, to automatically perform histogram equalization, to capture one or more frames and average them or apply one of several different processing algorithms to a captured frame. The report is in the form of a user manual for the software and includes guided tutorial and reference sections. A Digital Image Processing Primer in the appendix serves to explain the principle concepts that are used in the image processing. (rrh)http://archive.org/details/imageenhancement00partApproved for public release; distribution is unlimited

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Experimental Assessment and Enhancement of Planar Laser-Induced Fluorescence Measurements of Nitric Oxide in an Inverse Diffusion Flame

We have experimentally assessed the quantitative nature of planar laser-induced fluorescence (PLIF) measurements of NO concentration in a unique atmospheric pressure, laminar, axial inverse diffusion flame (IDF). The PLIF measurements were assessed relative to a two-dimensional array of separate laser saturated fluorescence (LSF) measurements. We demonstrated and evaluated several experimentally-based procedures for enhancing the quantitative nature of PLIF concentration images. Because these experimentally-based PLIF correction schemes require only the ability to make PLIF and LSF measurements, they produce a more broadly applicable PLIF diagnostic compared to numerically-based correction schemes. We experimentally assessed the influence of interferences on both narrow-band and broad-band fluorescence measurements at atmospheric and high pressures. Optimum excitation and detection schemes were determined for the LSF and PLIF measurements. Single-input and multiple-input, experimentally-based PLIF enhancement procedures were developed for application in test environments with both negligible and significant quench-dependent error gradients. Each experimentally-based procedure provides an enhancement of approximately 50% in the quantitative nature of the PLIF measurements, and results in concentration images nominally as quantitative as LSF point measurements. These correction procedures can be applied to other species, including radicals, for which no experimental data are available from which to implement numerically-based PLIF enhancement procedures

Facets of the ecology, behaviour and evolution of ants

SIGLEAvailable from British Library Document Supply Centre- DSC:DX178611 / BLDSC - British Library Document Supply CentreGBUnited Kingdo

The influence of hydroxyapatite nanoparticles on human mesenchymal stromal cells : application in tissue engineered constructs

PhD ThesisOsteoarthritis (OA) is a debilitating disease characterised by degradation of the articular cartilage and changes in the subchondral bone. Presently the gold standard treatment for OA is total joint replacement using metal, ceramic and non-degradable polymer materials. Tissue engineering using novel bioresorbable biomaterials has the potential to stimulate regeneration of bone and cartilage for early stage intervention in OA suffers. This thesis investigates the synthesis of hydroxyapatite nanoparticles (HAp) and techniques to generate poly (lactic acid) (PLA) HAp nanocomposites. The effect of the synthesised HAp on isolated OA donor derived human mesenchymal stem cells (hMSC) was investigated in both 2D and 3D culture conditions. A highly controllable sol-gel synthesis method demonstrated control over HAp morphology and composition, with modification of titration rate, addition methodology and reaction pH. Two novel nanocomposite fabrication techniques were developed and characterised with transmission electron microscopy (TEM) demonstrating HAp dispersion at the nanoscale throughout PLA. Dip-coated HAp PLA and fibrin substrates were fabricated and demonstrated maintenance of hMSC adherence, proliferation and osteogenesis on 2D substrates. Investigations into fibrin encapsulated hMSC illustrated HAp uptake within the cell following 24 hours incubation. Further studies examining fibrin/HAp encapsulated hMSC showed increased osteogenic gene expression, peripheral matrix deposition and mineralisation following 21 days in culture. 3D printed PLA constructs infused with fibrin and fibrin/HAp encapsulated hMSC demonstrated significant osteogenic gene expression differences at day 21. However, these data were variable between cell isolations from different patients further illustrating hMSC heterogeneity and hMSC donor–donor variability in-vitro.Arthritis Research U

The isolated muscle fibre as a model of disuse atrophy: characterization using PhAct, a method to quantify f-actin

Research into muscle atrophy and hypertrophy is hampered by limitations of the available experimental models. Interpretation of in vivo experiments is confounded by the complexity of the environment while in vitro models are subject to the marked disparities between cultured myotubes and the mature myofibres of living tissues. Here we develop a method (PhAct) based on ex vivo maintenance of the isolated myofibre as a model of disuse atrophy, using standard microscopy equipment and widely available analysis software, to measure f-actin content per myofibre and per nucleus over two weeks of ex vivo maintenance. We characterize the 35% per week atrophy of the isolated myofibre in terms of early changes in gene expression and investigate the effects on loss of muscle mass of modulatory agents, including Myostatin and Follistatin. By tracing the incorporation of a nucleotide analogue we show that the observed atrophy is not associated with loss or replacement of myonuclei. Such a completely controlled investigation can be conducted with the myofibres of a single muscle. With this novel method we can identify those features and mechanisms of atrophy and hypertrophy that are intrinsic to the muscle fibre from those that include activities of other tissues and systemic agents

Atmospheric oxygen tension slows myoblast proliferation via mitochondrial activation

Mitochondrial activity inhibits proliferation and is required for differentiation of myoblasts. Myoblast proliferation is also inhibited by the ~20% oxygen level used in standard tissue culture. We hypothesize that mitochondrial activity would be greater at hyperoxia (20% O(2)) relative to more physiological oxygen (5% O(2)).Murine primary myoblasts from isolated myofibres and conditionally immortalized H-2K myoblasts were cultured at 5% and 20% oxygen. Proliferation, assayed by cell counts, EdU labeling, and CFSE dilution, was slower at 20% oxygen. Expression of MyoD in primary myoblasts was delayed at 20% oxygen, but myogenicity, as measured by fusion index, was slightly higher. FACS-based measurement of mitochondrial activity indicators and luminometric measurement of ATP levels revealed that mitochondria exhibited greater membrane potential and higher levels of Reactive Oxygen Species (ROS) at 20% oxygen with concomitant elevation of intracellular ATP. Mitochondrial mass was unaffected. Low concentrations of CCCP, a respiratory chain uncoupler, and Oligomycin A, an ATP synthase inhibitor, each increased the rate of myoblast proliferation. ROS were investigated as a potential mechanism of mitochondrial retrograde signaling, but scavenging of ROS levels by N-acetyl-cysteine (NAC) or α-Phenyl-N-tert-butylnitrone (PBN) did not rescue the suppressed rate of cell division in hyperoxic conditions, suggesting other pathways. Primary myoblasts from older mice showed a slower proliferation than those from younger adult mice at 20% oxygen but no difference at 5% oxygen.These results implicate mitochondrial regulation as a mechanistic explanation for myoblast response to oxygen tension. The rescue of proliferation rate in myoblasts of aged mice by 5% oxygen suggests a major artefactual component to age-related decline of satellite cell proliferation in standard tissue culture at 20% oxygen. It lends weight to the idea that these age-related changes result at least in part from environmental factors rather than characteristics intrinsic to the satellite cell