Coralline Skeleton Biomaterial Reduces Phagocytosis in Mouse Blood in vitro

Inflammatory and immunogenic response to foreign bodies presents a challenge in the use of biomaterials as implants for tissue restoration. Therefore, there is a need to understand the interactions between such implants and the blood. One such material, currently in clinical use for bone replacement in humans, is the skeleton of corals, in the form of crystalline aragonite. This biomaterial has been shown to impart a protective and supportive influence on several types of cells ex vivo. The carbonate skeleton activates secretion in phagocytes in vitro, however its effects on these cells in the blood, and on the process of phagocytosis itself, remain unknown. Using 1–500 μm particles of coral skeleton, we show that these particles bind blood proteins and alter the leukocyte population, reducing the proportion of granulocytes by more than 3-fold with no effect on the proportion of monocytes. In addition, the presence of coral skeleton in the blood causes a reduction in phagocytosis. Specifically, we observed a decrease in the percentage of phagocytic cells by 27 % in the granulocytes and by 73 % in monocyte family, as well as a 41.6 % reduction in the MFI of granulocytes, but with no such effect on monocytes. Taken together, the results suggest that the coral skeleton biomaterial may act as a strong, promotive scaffold for tissue regeneration due to its ability to reduce its rejection by inflammatory reactions such as phagocytosis.     

High-Order Numerical Methods for 2D Parabolic Problems in Single and Composite Domains

In this work, we discuss and compare three methods for the numerical approximation of constant- and variable-coefficient diffusion equations in both single and composite domains with possible discontinuity in the solution/flux at interfaces, considering (i) the Cut Finite Element Method; (ii) the Difference Potentials Method; and (iii) the summation-by-parts Finite Difference Method. First we give a brief introduction for each of the three methods. Next, we propose benchmark problems, and consider numerical tests—with respect to accuracy and convergence—for linear parabolic problems on a single domain, and continue with similar tests for linear parabolic problems on a composite domain (with the interface defined either explicitly or implicitly). Lastly, a comparative discussion of the methods and numerical results will be given.     

Experimental analysis of the Poynting vector characteristics

The possibility of experimental measurement of the Poynting vector characteristics is shown. Under paraxial approximation, these characteristics may be obtained on the basis of local Stokes polarimetry and interferometry of electric field components. The experimental results for elliptically polarized Gaussian beam and heterogeneously polarized elementary fields are presented.     

The use of fluorescence lifetime imaging (FLIM) for in situ microbial detection in complex mineral substrates

The utility of fluorescence lifetime imaging microscopy (FLIM) for identifying bacteria in complex mineral matrices was investigated. Baseline signals from unlabelled Bacillus subtilis and Euglena gracilis, and Bacillus subtilis labelled with SYTO 9 were obtained using two-photon excitation at 730, 750 and 800 nm, identifying characteristic lifetimes of photosynthetic pigments, unpigmented cellular autofluorescence, and SYTO 9. Labelled and unlabelled B. subtilis were seeded onto marble and gypsum samples containing endolithic photosynthetic cyanobacteria and the ability to distinguish cells from mineral autofluorescence and nonspecific dye staining was examined in parallel with ordinary multichannel confocal imaging. It was found that FLIM enabled discrimination of SYTO 9 labelled cells from background, but that the lifetime of SYTO 9 was shorter in cells on minerals than in pure culture under our conditions. Photosynthetic microorganisms were easily observed using both FLIM and confocal. Unlabelled, nonpigmented bacteria showed weak signals that were difficult to distinguish from background when minerals were present, though cellular autofluorescence consistent with NAD(P)H could be seen in pure cultures, and phasor analysis permitted detection on rocks. Gypsum and marble samples showed similar autofluorescence profiles, with little autofluorescence in the yellow-to-red range. Lifetime or time-gated imaging may prove a useful tool for environmental microbiology. LAY DESCRIPTION : The standard method of bacterial enumeration is to label the cells with a fluorescent dye and count them under high-power fluorescence microscopy. However, this can be difficult when the cells are embedded in soil and rock due to fluorescence from the surrounding minerals and dye binding to ambiguous features of the substrate. The use of fluorescence lifetime imaging (FLIM) can disambiguate these signals and allow for improved detection of bacteria in environmental samples.     

Carbon fixation by the phytoplankton community across Lake Winnipeg

Lakes are important sites for carbon fixation and carbon dioxide (CO₂) exchange with the atmosphere. Carbon fixation rates have not previously been published for Lake Winnipeg but are important for quantifying the lake’s role in the regional greenhouse gas budget and the lake’s trophic structure and fish habitat. This study measured net ecosystem production (NEP), gross primary production (GPP), and gross respiration (GR) across the lake using a custom-built automated incubator connected to a ship’s water intake during a research cruise between July 31 and August 17, 2018 on Lake Winnipeg. The incubator estimated NEP, GR, and GPP every 60 min while moving along the ship’s track and at anchor, providing high-resolution data that are not obtainable through conventional incubations. The mean NEP for Lake Winnipeg during our survey was ?8.4 ± 5.6 g C m^?2 d^?1, suggesting that the lake was net heterotrophic and thus a net CO₂ source to the atmosphere during the 2018 summer cruise. The high-resolution data revealed significant spatiotemporal variability, including short-lived, highly net productive events that preceded remotely sensed chlorophyll a blooms by several days. Conversely, in regions with high chlorophyll a concentrations, we observed strong net heterotrophy and low nutrients, suggesting respiration was fueled by the degradation of mature, nutrient-limited phytoplankton blooms. The incubator system used in this study demonstrated its utility for monitoring rapid changes in NEP over short spatial scales in a lake which shows heightened regional variability in its physical, biogeochemical, and biological make-up.     

Structural Modifications in Bilayered Molecular Systems Lead to Predictable Changes in Their Electronic Properties

This study uses a novel surface engineering approach to demonstrate the influence of organic functional group substitutions on molecular electronic properties. Specifically, bilayered organic monomolecular systems immobilized on an inorganic electrode as the charge‐injecting components of organic electronic devices are compared. Recent literature reports demonstrate that structural modification in functional monolayers have unpredictable effects on their electronic properties. These studies indicate that the structure most certainly plays an important role, but its effect on the molecular resistance is diminished due to differences in other monolayer parameters. It is demonstrated that a separate control over the monolayer geometry and its chemical structure is required in order to observe predictable structure‐property relations. Here, bilayered molecular interfaces, comprising inert and functional layers whose properties can be independently controlled, are formed. It is shown that 1) the charge transfer through the bilayered system is sensitive to small structural molecular changes; 2) that it can be controlled and predicted by controlling the electron‐withdrawing or donating nature of the organic moiety; and 3) that the differences in the charge transfer dynamics of two bilayered systems can be visualized via patterned electroluminescence.