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Axio cam erc 5 s imaging system

Manufactured by Zeiss
Sourced in Germany

The Axio Cam ERc 5 s is a digital microscope camera system developed by Zeiss. It is designed for high-quality image capture and documentation of microscopic samples. The camera features a 5-megapixel CMOS sensor and supports a wide range of imaging modes, including brightfield, phase contrast, and fluorescence. The Axio Cam ERc 5 s is intended to provide reliable and accurate image data for various scientific and industrial applications.

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6 protocols using axio cam erc 5 s imaging system

1

Lichen Specimen Examination and Imaging

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The samples collected from South Korea were preserved in Korean Lichen Research Institute. Specimen examination and hand-sectioning was conducted under a dissecting microscope (SMZ 745T; Nikon, Tokyo, Japan). All anatomical descriptions are based on observations of these preparations under an Olympus BX 50 microscope (Tokyo, Japan) and photos were acquired under a Carl Zeiss MicroImaging microscope with Axio Cam ERc 5s imaging system (Jena, Germany). All measurements of the sections were conducted in water. The dimension range of ascospores was determined by measuring 30–50 ascospores.
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2

Morphological and Metabolite Characterization of Lichens

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All newly collected specimens included in this study were deposited in Sunchon National University, Korean Lichen Research Institute (KoLRI). The morphology examination and anatomical characteristics were recorded under a dissecting microscope (Model SMZ 745 T; Nikon, Tokyo, Japan) and Olympus BX 50 microscope (Olympus, Tokyo, Japan), and photographs were taken using a HD-Measure LTHS-300 (Leetech Co., Seoul, South Korea) microscope and Carl Zeiss MicroImaging with Axio Cam ERc 5 s imaging system (Carl Zeiss, Gottingen, Germany). The minimum (min.) and maximum values (max.) of the thallus width, soredia, apothecia, and ascospore size are recorded. The number (N) and mean values (in italics) were measured. Secondary metabolites were studied by a spot test and thin layer chromatography in solvent C, as described in [22 ] and [23 ]. UV test was performed with a UV Chamber (VL-6.LC; Viber Lourmat, Collégien, France) under a long (366 nm) wavelength.
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3

Morphological and Anatomical Characterization of Lichens

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The morphological and anatomical characteristics of the specimens were examined under a dissecting microscope (Nikon SMZ 745 T; Tokyo, Japan) and Olympus BX 50 microscope (Olympus, Tokyo, Japan). Photos were taken under HD-Measure LTHS-300 (Leetech Co., Seoul, South Korea) microscope and Carl Zeiss MicroImaging with Axio Cam ERc 5 s imaging system (Carl Zeiss MicroImaging, GmbH, Gottingen, Germany). All measurements based on the sections from thallus and apothecia were made in the water. Minimum-maximum values and the maximum value are recorded for granule, asci, and ascospores size. The number (N) of granules, asci, and spores were measured, and mean values (in italics), standard deviations (S.D.), quotient of length and width (Q), and average quotient [Q (m)] were calculated. The terminology to describe leprose lichens follows Lendemer [13 ].
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4

Lichen Specimen Collection and Analysis

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Three specimens in this study were collected from South Korea and deposited at Sunchon National University, Korean Lichen Research Institute (KoLRI). Morphological and anatomical characters were recorded under a dissecting microscope (Nikon SMZ 745 T, Tokyo, Japan) and an Olympus BX 50 microscope (Olympus, Tokyo, Japan), and images were captured using an HD-Measure LTHS-300 (Leetech Co., Seoul, South Korea) microscope and a Carl Zeiss MicroImaging with Axio Cam ERc 5 s imaging system (Carl Zeiss MicroImaging, GmbH 37081, Gottingen, Germany). The secondary metabolites were studied using the spot test (K = 10% aqueous KOH solution; C = saturated aqueous Ca(ClO)2; KC = 10% aqueous KOH solution followed by saturated aqueous Ca(ClO)2; PD = 5% alcoholic p-phenylenediamine solution) and thin-layer chromatography (TLC) in solvent C [15 ,16 ]. UV tests were performed using a UV Chamber (CE07 21470) under long (366 nm) wavelength.
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5

Lichen Specimen Collection and Morphological Analysis

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Specimens in this study were collected from South Korea and deposited in Sunchon National University, Korean Lichen Research Institute (KoLRI). Tracing observations of field growth status on the population of S. sinensis in Yeosu were conducted biweekly. Morphology examination and anatomical characters were recorded under a dissecting microscope (Nikon SMZ 745 T; Nikon, Tokyo, Japan) and Olympus BX 50 microscope (Olympus, Tokyo, Japan), and photographs were taken under HD-Measure LTHS-300 (Leetech Co., Seoul, Korea) microscope and Carl Zeiss MicroImaging with Axio Cam ERc 5 s imaging system (Carl Zeiss MicroImaging, Gottingen, Germany).
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6

Lichen Morphology and Anatomy Analysis

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All the specimens in this study were collected from South Korea and deposited in Sunchon National University, Korean Lichen Research Institute (KoLRI). Specimens morphology, and spot test were examined under a dissecting microscope (Nikon SMZ 745 T, Tokyo, Japan), and the anatomical characters were recorded under Olympus BX 50 microscope (Olympus, Tokyo, Japan) and photos under Carl Zeiss MicroImaging with Axio Cam ERc 5 s imaging system (Carl Zeiss MicroImaging, Göttingen, Germany). All measurements based on the sections from the thalli and apothecia were made in the water or KOH solution (5–10%). The ranges of ascospore dimensions were calculated from 30 to 50 ascospore size measurements of a single apothecium per specimen.
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