Find research datasets worth reusing

opennotspecifiedMar 2024View details →

FIGURE 1 in Lilium shenxianjuense (Liliaceae), a new species from Zhejiang, China

FIGURE 1. Gene map of the Lilium shenxianjuense plastome. The thick lines on the outer complete circle identify the inverted repeat regions (IRa and IRb). Genes on the outside and inside of the map are transcribed in clockwise and counter directions, respectively. Dashed area in the inner circle indicates the GC content.

opennotspecifiedMar 2024View details →

FIGURE 3. Lilium shenxianjuense. A, B. Habitat. C. Habit. D. Bulb. E. Stem with leaves. F. Indumentum. G. Inflorescence. H in Lilium shenxianjuense (Liliaceae), a new species from Zhejiang, China

FIGURE 3. Lilium shenxianjuense. A, B. Habitat. C. Habit. D. Bulb. E. Stem with leaves. F. Indumentum. G. Inflorescence. H. Tepals, stamens and pistil. I. Stamens and pistil.

opennotspecifiedSep 2015View details →

FIGURE 2 in Continuous variation supports accommodating Lilium habaense and L. xanthellum within L. stewartianum (Liliaceae)

FIGURE 2. Continuous variation within one population of Lilium xanthellum or of my inclusive L. stewartianum in Xiangcheng, Sichuan.—A. Four individuals exhibiting differences in the amount of tepal spots and in filament length.—B, C. the ridges at the base of the tepal show different prominence of projections at early (B) and late (C) stages.—D, E. Two flowers showing variation in the amount of spots on tepals.

opennotspecifiedSep 2015View details →

FIGURE 1 in Continuous variation supports accommodating Lilium habaense and L. xanthellum within L. stewartianum (Liliaceae)

FIGURE 1. An illustration of features traditionally used to delimit Lilium habaense, L. stewartianum, and L. xanthellum.

opennotspecifiedJun 2015View details →

FIGURE 1 in Lilium saccatum: A new synonym of L. souliei (Liliaceae) for Flora of China

FIGURE 1. Images of type specimens of Lilium souliei (Franchet) Sealy (A) and L. saccatum S.Y. Liang (B). The right side shows each enlarged part of flora (highlighted in the black box on the types) which demonstrated both species have a basally saccate teples (indicated by the arrow).

opennotspecifiedSep 2016View details →

FIGURE 3 in Accommodating Nomocharis in Lilium (Liliaceae)

FIGURE 3. Field pictures of Lilium apertum in western Yunnan: a–c, population from Zhongdian, Yunnan showed spot variation; c–e, population of Fugong, Yunnan showed variations in tepal color; f–h, habits of L. apertum under different habitats; i–j, anatomical pictures showed two types of L. apertum from Zhongdian and Fugong, as well as a comparison of outer and inner tepals.

opennotspecifiedSep 2016View details →

FIGURE 1 in Accommodating Nomocharis in Lilium (Liliaceae)

FIGURE 1. Field pictures of western China Lilium (formerlly Nomocharis): a–c, L. basilissum; d–f, L. farreri; g–i, L. gongshanense; j–l, L. meleagrinum.

FIGURE 4 in Restore the name Lilium tenii H.Lév. (Liliaceae), which has priority over the later synonym L. lijiangense L.J.Peng

FIGURE 4. Specimen of Lilium lijiangense collected at the type locality of L. huidongense J.M.Xu (Y. D. Gao G20090729, SZ).

FIGURE 3 in Restore the name Lilium tenii H.Lév. (Liliaceae), which has priority over the later synonym L. lijiangense L.J.Peng

FIGURE 3. Pictures from the field of Lilium lijiangense L.J.Peng. A, habit; B, flower; C, stem and leaves; D, enlarged leaves showed seven to nine veins and white hairs at the leaf base (highlight by white circles).

FIGURE 1 in Restore the name Lilium tenii H.Lév. (Liliaceae), which has priority over the later synonym L. lijiangense L.J.Peng

FIGURE 1. One of the syntypes of Lilium tenii collected by Father Siméon Ten on 15 August 1907 (Ten P.S. 435, E00381814) from Dongchuan (Tong-Tchouan) of Yunnan Province, China.

FIGURE 2 in Restore the name Lilium tenii H.Lév. (Liliaceae), which has priority over the later synonym L. lijiangense L.J.Peng

FIGURE 2. One of syntypes of Lilium primulinum var. ochraceum collected by Delavay on 1 September 1882 (Delavay J.M. 369, P00730975) from Yunnan, China.

opennotspecifiedJun 2014View details →

FIGURE 2 in Taxonomic notes on Chinese Lilium L. (Liliaceae) with proposal of three nomenclatural revisions

FIGURE 2. Flowers of Lilium taliense Franchet from NW Yunnan showng continuous morphological variations in tepal spots andcolor i.e., white to yellow). Materials representing populations from A, Wengshui, Yunnan (Kham Expedition 10-56, PE) showing variability of spot tepal spots; B, Gezan, Yunnan (Kham Expedition 10-10, PE) showing variability of tepal color on a single individual; C, Jinfo Mountain, the type locality of L. jinfushanense exhibiting yellow inner tepals.

opennotspecifiedJun 2014View details →

FIGURE 1 in Taxonomic notes on Chinese Lilium L. (Liliaceae) with proposal of three nomenclatural revisions

FIGURE 1. Bulbs of Lilium brownii from different populations showing variable segmentation of the scales. A-B, Materials representing populations from Nanchuan, Chongqing (Gao G2010001, SZ) showing segmented (A) and unsegmented (B) scales, respectively; C, Jiangyou, Sichuan (WJ10051401, SZ); D, Lushui, Yunnan (Gao G2009002, SZ).

Fig. 4 in Molecular cloning, characterization and expression analysis of LoTPS2 and LoTPS4 involved in floral scent formation in oriental hybrid Lilium variety 'Siberia'

Fig. 4. Product analysis of LoTPS4 produced from GGPP and FPP. (a) GC-MS analysis (ion chromatogram) of the LoTPS4 enzyme product from GGPP. (b) GC-MS analysis (ion chromatogram) of products obtained from assays with LoTPS4 and FPP. (c, d, e, f) Mass spectra of Peak 1, Peak 2, Peak 3 and Peak 4. Di-epi-α-cedrene (Peak 1), α-cubebene (Peak 2): trans-α-bergamotene (Peak 3) and (E)-β-farnesene (Peak 4).

Fig. 3 in Molecular cloning, characterization and expression analysis of LoTPS2 and LoTPS4 involved in floral scent formation in oriental hybrid Lilium variety 'Siberia'

Fig. 3. (a) GC-MS analysis of products produced from assays with extracts of the empty vector and GPP. (b) Analysis (total ion chromatogram) of the product of the LoTPS4 enzyme generated from GPP (c) Total ion chromatogram of the D-limonene authentic standard. (d) Mass spectrum of the Peak 3 (e) Mass spectrum of Dlimonene in the floral scent of Lilium 'Siberia' (f) Mass spectrum of the D-limonene authentic standard (g, h, I and j) Mass spectra of Peak 1, Peak 2, Peak 4 and Peak 5. β-Phellandrene (Peak 1), β-myrcene (Peak 2), D-limonene (Peak 3), 3-Carene (Peak 4) and (+)-4-Carene (Peak 5).

Fig. 10 in Molecular cloning, characterization and expression analysis of LoTPS2 and LoTPS4 involved in floral scent formation in oriental hybrid Lilium variety 'Siberia'

Fig. 10. Subcellular localization of LoTPS2 and LoTPS4. Confocal laser scanning microscopy of LoTPS2 and LoTPS4 was performed by using EGFP fusion proteins in Arabidopsis protoplasts. The full-length coding region and the N-terminal 80 amino acids of the coding region of LoTPSs were fused to the GFP reporter gene in the p35 S vector to generate the p35 S-LoTPSs/GFP construct. The red column shows chlorophyll autofluorescence; the green column shows GFP fluorescence; the merged columns show combined GFP fluorescence and chlorophyll autofluorescence; and the BF columns represent bright field images. The names of the constructs are given on the left. HcTPS7 from H. coronarium was used as a marker. Scale bars: 5 μm. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Fig. 2 in Molecular cloning, characterization and expression analysis of LoTPS2 and LoTPS4 involved in floral scent formation in oriental hybrid Lilium variety 'Siberia'

Fig. 2. GC-MS analysis of products generated by LoTPS2. (a) GC-MS analysis (total ion chromatogram) of the products obtained by incubating extracts of the empty vector (control) with geranyl pyrophosphate. (b) GC-MS analysis (total ion chromatogram) of the LoTPS2 enzyme with GPP. (c) GC–MS analysis (total ion chromatogram) of the LoTPS2 enzyme with farnesyl pyrophosphate showing (E, E)-α- farnesene as the sole product. (d) Mass spectrum of the peak. (e) Mass spectrum of (E, E)-α-farnesene in the NIST08 library.

Fig. 7 in Molecular cloning, characterization and expression analysis of LoTPS2 and LoTPS4 involved in floral scent formation in oriental hybrid Lilium variety 'Siberia'

Fig. 7. Relative expression analysis of LoTPS2 and LoTPS4 during different flower development performed by quantitative real-time PCR. (a, b) Transcript levels of the LoTPS2 and LoTPS4 genes during flower development. (c, d) Relative expression analysis of LoTPS2 and LoTPS4 at different flower developmental stages. Flower development was divided into 5 different stages: D1 (bud stage), D2 (little open), D3 (half open), D4 (full-bloom), D5 (senescence). GAPDH was used as an internal control. The root was set as 1. Data are presented as the mean ± SEM (n = 3).

Fig. 8 in Molecular cloning, characterization and expression analysis of LoTPS2 and LoTPS4 involved in floral scent formation in oriental hybrid Lilium variety 'Siberia'

Fig. 8. Relative expression analysis of LoTPS genes and the emission of (E, E)-α-farnesene and D-limonene from Lilium 'Siberia' at different time intervals. (a, b) Expression pattern of LoTPS2 and LoTPS4 for 3 days postanthesis. (c) Emission pattern of (E, E)-α-farnesene from Lilium 'Siberia' (d) Emission pattern of D-limonene from Lilium 'Siberia' flowers over 3 days after full-bloom. The plants were kept under a 12 h light, 12 h dark photoperiod. GAPDH was used as an internal control. Each point is the average of 3 replicates.

Fig. 6 in Molecular cloning, characterization and expression analysis of LoTPS2 and LoTPS4 involved in floral scent formation in oriental hybrid Lilium variety 'Siberia'

Fig. 6. (a) A labeled diagram of a fullbloom Lilium 'Siberia' flower. (b) Pictorial view of Lilium 'Siberia' flowers at different flower developmental stages.