Gemological Characteristic Difference between Colorless CVD Synthetic Diamonds and Natural Diamonds

CVD synthetic diamond plays an important role in the jewelry market due to its excellent performance and low cost. In this paper, colorless CVD synthetic diamonds produced by a Chinese company were investigated in detail with their gemological, spectroscopic, and luminescent properties compared with natural colorless diamonds. Compared with natural diamonds, CVD synthetic diamonds have high-order interference color and more apparent abnormal birefringence. The results of infrared spectra indicate that all the CVD samples are classified as type IIa, while the natural samples belong to type Ia. The CVD samples show lamellar growth and mottled luminescence pattern and have blue, orange red, purple red, and blue fluorescence, respectively, while most of the natural samples show blue fluorescence. CVD diamonds show lamellar growth structure, and natural diamonds show irregular ring-like growth structure. Thus, multiple methods combined with analysis are required to distinguish synthetic diamonds from natural diamonds. This work provides an experimental basis for the identification of CVD synthetic diamonds.

Lumi-Map, a Real-Time Luciferase Bioluminescence Screen of Mutants Combined with MutMap, Reveals Arabidopsis Genes Involved in PAMP-Triggered Immunity

Plants recognize pathogen-associated molecular patterns (PAMPs) to activate PAMP-triggered immunity (PTI). However, our knowledge of PTI signaling remains limited. In this report, we introduce Lumi-Map, a high-throughput platform for identifying causative single-nucleotide polymorphisms (SNPs) for studying PTI signaling components. In Lumi-Map, a transgenic reporter plant line is produced that contains a firefly luciferase (LUC) gene driven by a defense gene promoter, which generates luminescence upon PAMP treatment. The line is mutagenized and the mutants with altered luminescence patterns are screened by a high-throughput real-time bioluminescence monitoring system. Selected mutants are subjected to MutMap analysis, a whole-genome sequencing-based method of rapid mutation identification, to identify the causative SNP responsible for the luminescence pattern change. We generated nine transgenic Arabidopsis reporter lines expressing the LUC gene fused to multiple promoter sequences of defense-related genes. These lines generate luminescence upon activation of FLAGELLIN-SENSING 2 (FLS2) by flg22, a PAMP derived from bacterial flagellin. We selected the WRKY29-promoter reporter line to identify mutants in the signaling pathway downstream of FLS2. After screening 24,000 ethylmethanesulfonate-induced mutants of the reporter line, we isolated 22 mutants with altered WRKY29 expression upon flg22 treatment (abbreviated as awf mutants). Although five flg22-insensitive awf mutants harbored mutations in FLS2 itself, Lumi-Map revealed three genes not previously associated with PTI. Lumi-Map has the potential to identify novel PAMPs and their receptors as well as signaling components downstream of the receptors. [Formula: see text] Copyright © 2020 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license .

Lumi-Map, a real-time luciferase bioluminescence screen of mutants combined with MutMap, reveals Arabidopsis genes involved in PAMP-triggered immunity

Plants recognize pathogen-associated molecular patterns (PAMPs) to activate PAMP-triggered immunity (PTI). However, our knowledge of PTI signaling remains limited. In this report, we introduce Lumi-Map, a high-throughput platform for identifying causative single nucleotide polymorphisms (SNPs) to studying PTI signaling components. In Lumi-Map, a transgenic reporter plant line is produced that contains a firefly luciferase (LUC) gene driven by a defense gene promoter, which generates luminescence upon PAMP treatment. The line is mutagenized and the mutants with altered luminescence patterns are screened by a high-throughput real-time bioluminescence monitoring system. Selected mutants are subjected to MutMap analysis, a whole genome sequencing (WGS)-based method of rapid mutation identification, to identify the causative SNP responsible for the luminescence pattern change. We generated nine transgenic Arabidopsis reporter lines expressing LUC gene fused to multiple promoter sequences of defense-related genes. These lines generate luminescence upon activation of FLAGELLIN-SENSING 2 (FLS2) by flg22, a PAMP derived from bacterial flagellin. We selected the WRKY29-promoter reporter line to identify mutants in the signaling pathway downstream of FLS2. After screening 24,000 ethylmethanesulfonate (EMS)-induced mutants of the reporter line, we isolated 22 mutants with altered WRKY29 expression upon flg22 treatment (abbreviated as awf mutants). While five flg22-insensitive awf mutants harbored mutations in FLS2 itself, Lumi-Map revealed three genes not previously associated with PTI. Lumi-Map has the potential to identify novel PAMPs and their receptors as well as signaling components downstream of the receptors.

CHATODOLUMINESCENCE MICROSCOPIC ANALYSIS TO INTERPRET THE REDOX CONDITION DURING THE FORMATION OF CARBONATE VEIN

Cathodoluminescence (CL) is generated by an electron gun coupled to an optical microscope. There are two types of chatodoluminescence, i.e., cold CL and hot CL. In the cold cathode microscopic equipment, the electrons are generated by an electric discharge between two electrodes under a low gas pressure, whereas in the hot CL microscope, the electrons are generated by heating a filament (2000–3000°C). In this paper we utilize cold CL combine with electron microprobe analysis (EMPA). The CL microscopy of carbonate shows at least three carbonate generations, i.e., rhodochrosite with dull or no luminescence, Mg-rich calcite with dark red luminescence, manganese-bearing calcite with up to 0.04 wt.% Mn with bright orange luminescence, and pure calcite and Mn-rich calcite (> 0.15 wt.% Mn) with dull or no luminescence. The result also suggests that the luminescence pattern of calcite is controlled by the amount of Mn2+. Sectoral zoning and chevron-shape growth zoning exist in some coarse-grained calcite aggregates. The sectorial zoning of calcite as reflected by dull to bright CL color indicated that slightly to more reducing environment during calcite deposition. Keywords: Chatodoluminescence, rhodochrosite, calcite, sectorial zoning

Camouflage by Disruptive Illumination in Leiognathids, a Family of Shallow-Water, Bioluminescent Fishes

Leiognathids are shallow-water, Indo-West Pacific fishes that have a circumesophageal, bacterial light organ. Visual observations of living fishes revealed a mottled ventral luminescence pattern, which was analyzed both behaviorally and morphologically. In behavioral experiments, these fishes responded to increases in intensity of downwelling light with increases in the intensity of ventral luminescence. However, while the absolute luminescence levels tracked the ambient light levels, they did not increase in direct proportion to those of increasing downwelling light; luminescence levels were closer to the intensity of downwelling light at low light levels. The tissues that intervene between the internal light organ and the external environment are responsible for the observed mottled pattern of the ventral luminescence. Furthermore, these tissues, which have been incorporated into the light organ system, are involved in the control of the intensity, spectral quality and angular distribution of the fish's luminescence. The spectral peak of the bacterial luminescence from whole fish (500 nm) was shifted about 10 nm towards the green relative to the spectral peak of cultured light organ symbionts (485–490 nm). The luminescence had the greatest intensity of outward expression at an angle of 20–25° from the ventral midline and was undetectable dorsally. The ventral illumination behavior of leiognathids, with their associated morphology, is compared and contrasted with the counterillumination systems that have been described in a number of mesopelagic fishes, shrimps and squids. Note: To whom reprint requests should be addressed at the Department of Biological Sciences, University of Southern California, Los Angeles, CA 90089–0371, USA.