Fig. 1. Wavelengths of fluorescent lamp ranging from 300 nm to 1,100 nm. Its maximum photoysnthetic photon flux density (PPFD) was 2.003 μmol/m2/s at 544 nm.
Fig. 2. Wavelengths of fluorescent lamp penetrated through cellophane filter ranging from 300 nm to 1,100 nm. Each light (red, green, blue) had its own wavelength in which the maximum photosynthetic photon flux density (PPFD) value was found.
Fig. 3. Photosynthetically active photon flux density (PPFD) under various wavelengths of light emitted diode (LED) lamp in far-red, red, green and blue. The maximum PPFD was at 732 nm by far-red, 650 nm by red, 520 nm by green, and 458 nm by blue.
Fig. 4. Browning of Lentinula edodes mycelial depending on existence of light. Browning occurred in the non-irradiated medium by 5% only of the colony area (left six plates), and browning occurred in the irradiated medium by 64% of the colony area (right six plates).
Fig. 5. Effects of light wavelengths on browning of Lentinula edodes mycelia cultured in potato dextrose agar (PDA) medium. A, In far-red (702~760 nm); B, Red (646~654 nm); C, Green (502~546 nm); D, Blue (442~480 nm); E, Fluorescent light (300~1,100 nm); F, Brown portion shown as black under fluorescent light.
Fig. 6. White and brown mycelia of Lentinula edodes cultured under different light wavelengths. A, White bumpy colony under red light (646~654 nm); B, Brown colony under blue light (442~480 nm); C, Enlarged white cottony colony surface, ⅹ20; D, Enlarged brown colony surface, ⅹ20; E, Soft thin wall hyaline hyphae on white colony, ⅹ600; F, Hard thick wall brown hyphae on brown colony surface, ⅹ 400.
Table 1. Wavelength and PPFD of LED sources used for browning and primordial formation of Lentinula edodes mycelial culture
Table 2. Browning area rate (%) in Lentinula edodes mycelial culture plates irradiated with various light wavelengths
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