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Optical materials composed of Ba9–3(m+n)/2ErmYbnY2Si6O24 (m = 0.005–0.2, n = 0–0.3) were prepared using a solid‐state reaction. The X‐ray diffraction patterns of the obtained phosphors were examined to index the peak positions. The photoluminescence (PL) excitation and emission spectra of the Er3+‐activated phosphors and the critical emission quenching as a function of Er3+ content in the Ba9–3m/2ErmY2Si6O24 structure were monitored. The spectral conversion properties of Er3+ and Er3+–Yb3+ ions doped in Ba9Y2Si6O24 phosphors were elucidated under diode‐laser irradiation at 980 nm. Up‐conversion emission spectra and the dependence of the emission intensity on pump power for the Ba8.55Er0.1Yb0.2Y2Si6O24 phosphor were investigated. The desired up‐conversion of the emitted light, which passed through the green, yellow, orange and red regions of the spectrum, was achieved through the use of appropriate Er3+ and/or Yb3+ concentrations in the host structure and 980 nm excitation light. The up‐conversion mechanism in the phosphors is described by an energy‐level schematic. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

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Salvia × westerae is described and illustrated, its floral characteristics being contrasted with those of its parents. The characteristics and distribution of the parent species, Salvia haenkei and S. orbignaei, are discussed and short biographies of their eponymous discoverers, Haenke and D'Orbigny are provided. Pollination syndromes in American Salvia are briefly discussed and the rare occurrence of natural hybrids in the Americas is noted.  相似文献   

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Species diagnosis is of the utmost importance to both pest management and plant quarantine services. Because of difficulties in the morphological diagnosis of spider mites, molecular techniques are of great value to rapidly and accurately diagnose closely related species. We examined four species of genus Tetranychus (the green and red forms of T. urticae, and T. kanzawai, T. phaselus and T. truncatus), which are found in Korea and are of significance to plant quarantine services. DNA samples isolated from a single egg, larva or adult weighed 64–188 ng. We designed species‐specific primers by performing sequence alignment for 107 sequences of the ribosomal internal transcribed spacer 2 (ITS2) region, which we obtained from GenBank, and sequences generated in this study. Specific nucleotides of each species were selected for designing primers specific for each species. Each species‐specific primer pair, when used to perform PCR analyses, detected only the species from which it originated. However, a T. urticae‐specific primer pair did not discriminate between the green and red forms of this species. These species‐specific primers can be applied in practice for the rapid and accurate diagnosis of spider mite species in plant quarantine and in agricultural fields.  相似文献   

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