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The surface morphology of treated mild steel examined by scanning electron microscope is shown in Fig. 10 for samples treated with 1N hydrochloric acid solution, Fig. 11 for samples treated with 1N sulfuric acid solution, and Fig. 12 for sample treated with HNO3 solution.
A photograph of the pressurized chamber on the stage of an Olympus IX71 inverted optical microscope is shown in Fig. S1A.
The cell surface as seen under the scanning electron microscope is shown in Figure 1A, to contrast with subsequent images of attached spirochetes.
The setting of the flowcell within the laser scanning confocal microscope is shown in Figure 1.
The distribution of the intracellular Fe granules observed under transmission electron microscope is shown in Figures 5 e)- 5(f).
A schematic of a high-speed SRS microscope is shown in Figure 4. Key components needed for SRS imaging include a dual-color laser source, an optical modulator, a laser scanner, a detector, and an electronic demodulator.
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Reduction in the amount of fibroblast cells 3T3-A31 treated with the fresh xylem sap and fisetin visualized by inverted light microscope is showed in Figure 3.
The photographs of wet, freeze-dried, and air-dried beads, taken under an optical microscope, are shown in Figure 1.
DF image from the agglomerate and diffractions before and after heating in the column of microscope are shown in the insets Fig. 5 Composite particles in Ni49.9Ti40.3Zr0.3Cu0.1Hf9.4 powder.
In Fig. 10, TEM micrographs of the grain boundary in focus (a c) as obtained with each microscope are shown as well as the finally calculated intensity derivatives (d f) and the corresponding reconstructed phase images (g i).
Images taken by a coupled charge camera device (CCD) connected to the inverted microscope are shown in Fig. 2. As a control experiment, the excitation of a bare and conjugated ZnO NRs was first performed.
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