Amana hejiaqingii (Liliaceae), a New Species from the Dabie Mountains, China
by
, and
Meizhen Wang
1
,
Shenglu Zhang
1,
Jing Wu
1,
Xinxin Zhu
2,
Zongcai Liu
3,
Gengyu Lu
4 and
Pan Li
1,* 1
Laboratory of Systematic & Evolutionary Botany and Biodiversity, College of Life Sciences, Zhejiang University, Hangzhou 310058, China
2
College of Life Sciences, Xinyang Normal University, Xinyang 464000, China
3
College of Life Science and Agricultural Engineering, Nanyang Normal University, Nanyang 473061, China
4
Department of Resources Science of Traditional Chinese Medicines, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 211198, China
*
Author to whom correspondence should be addressed.
Taxonomy 2022, 2(3), 279-290; https://doi.org/10.3390/taxonomy2030022
Submission received: 14 June 2022
/
Revised: 29 June 2022
/
Accepted: 30 June 2022
/
Published: 4 July 2022
Abstract
:In this paper, a new species from Central China, Amana hejiaqingii (Liliaceae), is described and illustrated. It resembles A. anhuiensis and A. tianmuensis but differs from A. anhuiensis as it has one white vein on its lower leaf and yellow anthers. It also differs from A. tianmuensis by possessing solitary pink flowers with longer and wider tepals. The principal coordinates analysis separated the three species based on morphological data. Cytological observation showed that A. hejiaqingii is diploid (2n = 2x = 24). Molecular phylogenetic analyses further supported its species delimitation.
1. Introduction
The genus Amana Honda (1935: 20; Liliaceae) is characterized by 2−3(–4) opposite or verticillate bracts at the upper part of flowering stem and a distinct beak of the fruit, which separates it from Tulipa L. (Tan et al., 2005 [1]). Amana consists of nine perennial herbaceous species and is endemic to East Asia (Ohwi and Kitagawa 1992 [2]; Chen and Mordak 2000 [3]; Shen 2001 [4]; Tan et al., 2007 [5]; Tan et al., 2008 [6]; Han et al., 2014 [7]; Li et al., 2017 [8]; Wang et al., 2019 [9]; Wang et al., 2022 [10]). Amana belongs to spring ephemerals, blooming in early spring. The above-ground tissues die after bearing fruit and become dormant underground (Struik, 1965 [11]). This genus mainly occurs in temperate deciduous or subtropical evergreen broadleaved/mixed forests. Amana is diploid, and its basic chromosome number is x = 12, except for two ploidy levels in A. edulis: diploid in northern populations and tetraploid in southern populations (Wang et al., 2022 [10]; Wu et al., 2022 [12]). This genus is confirmed to be in a monophyletic group and sister clade with Erythronium (Li et al., 2017 [8]). A suspected new species was found during fieldwork from 2016 to 2022 in the Dabie Mountains, China. Our morphological examination and phylogenetic analyses further verified that it is a new species. Therefore, we describe and illustrate it here.
2. Materials and Methods
2.1. Sampling, Sequencing and Assembly
The new species was investigated in eight localities in the Dabie Mountains bordering the Henan and Hubei provinces from 2016 to 2022 (Figure 1). Genomic DNA was extracted from silica-gel-dried leaves with modified CTAB reagent (Plant DNAzol, Shanghai, China), according to the manufacturer’s protocol. Libraries were pooled and sequenced with 150 bp paired-end reads using the Illumina HiSeq X10 platform at China National GeneBank (CNGB, Shenzhen, China). Raw reads were assembled into plastome sequences by GetOrganelle (Jin et al., 2020 [13]) with default settings. The newly generated sequences can be accessed on GenBank (Table 1). Voucher specimens were deposited at the Herbarium of Zhejiang University (HZU, acronyms according to Thiers et al., 2016 [14]).
2.2. Morphological Observation and Principal Coordinates Analysis
Morphological observations served as the basis of species description. Morphological traits of bulbs, bracts, leaves, flowers and fruits were measured and recorded. Herbarium specimens from CDBI, CSH, HHBG, HIB, HZU, IBSC, KUN, LBG, NAS, PE, WUK (acronyms according to Thiers et al., 2016 [14]) were examined for comparison. Additionally, a morphological comparison was made among Amana anhuiensis (X.S. Shen) D.Y. Tan & D.Y. Hong, Amana tianmuensis P. Li & M.Z. Wang and Amana hejiaqingii. Eleven traits were applied for principal coordinates analysis with R package vegan v.2.6.2 and ggplot2 v.3.3.6 (Wickham 2016 [15]), including the position of the widest part of lower leaf (top: 0; upper: 1), number of white veins on lower leaf, bracts length, bracts width, shape of bracts (linear: 0; lanceolate: 1), color of flowers (white: 0; pink: 1), outer tepal length, outer tepal width, inner tepal length, inner tepal width and color of anthers (yellow: 0, light-purple: 1). A total of 52 individuals (7 of A. anhuiensis from three populations, 23 of A. hejiaqingii from six populations and 22 of A. tianmuensis from eight populations) were measured for analysis (Table S1).
2.3. Cytological Analysis
Actively growing droppers were collected in the field for chromosome counting. The dropper tip materials were pretreated in 0.1% colchicine for 4.5 h and then fixed in Carnoy’s Fluid (3 absolute alcohol: 1 glacial acetic acid, v/v) for 12–24 h. Afterwards, they were converted into anhydrous ethanol and stored at −20 °C in the refrigerator for further treatment. The fixed dropper tips were bathed in 37 °C enzyme solution (a mixture of 2% cellulase and pectinase (2:1)) for 1 h. After hydrolysis, the materials were rinsed with distilled water several times. Finally, stained tips with Carbol fuchsin and chromosome compression tablets were made for observation. Photos were captured by a SOPTOP DMCX40 microscope (SOPTOP, Ningbo, China).
Karyotype formula was based on the measurement of mitotic metaphase chromosomes photos. The degree of karyotype asymmetry (As.K%, Arano 1963), karyotypic symmetry division category (KA Type, Stebbins 1971 [16]), mean centromeric asymmetry index (MCA), coefficient of variation of chromosome length (CVCL), coefficient of variation (CVCI), and total haploid karyotype length (THL) were evaluated (Paszko 2006, [17] Peruzzi et al., 2009 [18], Peruzzi and Eroğlu 2013 [19], Peruzzi and Altınordu 2014 [20]). KaryoType software was used to measure the indices of karyotype asymmetry (Altınordu et al., 2016 [21]).
2.4. Phylogenetic Analyses
A total of 28 individuals representing 13 species were included. Erythronium sibiricum (Fisch. & C.A. Mey.) Krylov, Tulipa altaica Pall. ex Spreng. and Lloydia tibetica Baker ex Oliv. were used as outgroups based on their close phylogenetic relationships with Amana (Lu et al., 2021 [22]). The 76 common plastid CDS genes were extracted and concatenated for phylogenetic analyses in Geneious v.4.8.5 (Kearse et al., 2012 [23]). Phylogenetic reconstructions were conducted using IQ-TREE 2 (Minh et al., 2020 [24]) for maximum likelihood (ML) analyses with 1000 bootstrap replicates and Modelfinder (Kalyaanamoorthy et al., 2017 [25]) for gene partitions. Finally, 16 kinds of best partition schemes were found. Bayesian inference (BI) was implemented on MrBayes v.3.2.7a (Ronquist et al., 2012 [26]) with GTR + I + G substitution model. The Markov chain Monte Carlo (MCMC) algorithm was run with two independent chains and default priors for 10,000,000 generations. Trees were sampled every 1000 generations.
3. Results
3.1. Morphological Comparisons
Amana hejiaqingii (Figure 2 and Figure 3) is similar to A. anhuiensis (Figure 4) and A. tianmuensis (Wang et al., 2022 [10]) in bulbs, leaves and flowers. However, it differs from A. anhuiensis as it has lower leaves with a grayish-white midvein (vs. with more than one white vein), and yellow anthers (vs. light-purple) at maturity. Additionally, the widest part of the lower leaf of A. hejiaqingii is usually in the 2/8–3/8 position (upper part) of the leaf, while A. anhuiensis is usually at 1/8 position (top part) of the leaf. Meanwhile, it differs from A. tianmuensis as it has a solitary pink flower (vs. mostly solitary, sometimes two, white). Moreover, the outer and inner tepals of A. hejiaqingii were mostly longer and wider than A. tianmuensis (Table 2).
3.2. Principal Coordinates Analysis
A principal coordinates analysis showed three separated clusters (Figure 5). The first principal coordinates (PCoA1) accounted for 31.77%, and the second principal coordinates (PCoA2) accounted for 13.34% of the total variance.
3.3. Cytology Observation
A total of six populations were observed, and the numbers of metaphase chromosomes were 2n = 2x = 24 = 3 m + 11 sm + 10 st. The length of chromosome varied from 5.75 to 10.05 μm. The ratio of the longest to shortest chromosome was 2.13. The total haploid length of the chromosome set (THL) was 99.10. The coefficient of variation of centromeric index (CVCI) was 18.83. The coefficient of variation of chromosome length (CVCL) was 11.60. The mean centromeric asymmetry (MCA) was 50.42. As.K% was 75.50. KA belonged to Stebbins’s—3B (Figure 6).
3.4. Molecular Phylogeny
The complete plastome sequence length of Amana hejiaqingii was 151,513–151,516 bp (large single copy (LSC) 81,862–81,864 bp, small single copy (SSC) 17,107–17,112 bp and inverted repeat (IR) 26,271 bp with 36.7%, 34.6%, 30.1% and 42% GC content; Figure S1). The total alignment was 73,033 bp with 3065 variable sites. The phylogenetic tree based on plastid genes (Figure 7) revealed that A. hejiaqingii was distantly related to A. tianmuensis with robust supports (BIPP = 1.0, MLBS = 100). This finding is congruent with our ongoing phylotranscriptomic study on the genus Amana.
4. Taxonomy
Amana hejiaqingii M.Z. Wang & P. Li, sp. nov. (大别老鸦瓣 is the Chinese name of Amana hejiaqingii. Figure 2 and Figure 3)
Type: CHINA. Henan Province: Xinyang City, Shangcheng County, Fushan Town, Liluocheng (里罗城), in deciduous broadleaf forest, 31°43′14.4″ N, 115°30′12.5″ E, 487 m, 15 February 2022, Pan Li et al. WMZ1722 (holotype HZU, isotype HZU, PE, KUN, CSH, HIB, WH, ZM).
Diagnosis: This new species resembles Amana tianmuensis P. Li & M.Z. Wang in possessing yellowish-brown, thinly papery bulb tunics, oblanceolate leaves and three verticillate linear bracts, but differs from it as it has solitary pink flower (vs. solitary, sometimes two, white) with longer wider tepals.
Description: Perennial herbs. Bulb ovoid, 0.9–2.3 cm in diameter, tunics yellowish-brown, thinly papery, glabrous, sometimes sparely villous inside. Stem 1.1–12.3 cm tall, glabrous, simple. Leaves usually two, opposite, green, adaxially middle grayish white, oblanceolate, glabrous; the lower leaf 8–26.6 × 1.0–2.8 cm, the upper 7.7–26 × 0.5–1.4 cm, and leaves can reach 34 cm long at fruiting stage. Bracts usually three, verticillate, linear, green, 1.2–4.2 × 0.1–0.3 cm, and bracts can be flat and slightly curved at fruiting stage. Scape 5.1–14.2 cm tall, glabrous, simple. Pedicel 0.5–4.1 cm. Flower solitary, funnel-shaped; tepals six, pink, with a yellowish-green blotch at the very base inside and green-yellowish or purple-red streaks on the back; outer tepals lanceolate, acute, 2.4–4.4 × 0.6–1.1 cm, inner tepals narrow elliptic, acute, 2.1–3.9 × 0.6–1.0 cm. Stamens six, two-wheeled, the inner three slightly longer than the outer; filaments yellowish-green, 3–13 mm long, proximally dilated, gradually attenuate towards apex, glabrous. Anthers yellow, 5–15 mm long. Ovaries oval, yellowish-green, constricted below the style, 0.3–0.7 cm long. Style 0.4–0.6 cm long. Fruit capsule subglobose, triquetrous, 0.7–1.4 cm in diameter, apex long beaked, 0.5–1.2 cm long. Fl. January–March, Fr. March–May.
Distribution and habitat: Up to now, Amana hejiaqingii is found in eight localities across 233.7 km in the Dabie Mountains bordering Henan and Hubei provinces. It grows in moist deciduous broad-leaf forests on mountain slopes at elevations of 70–530 m. In future investigations, we think that more populations will be found in the area in and around these localities.
Etymology: The specific epithet is named in memory of Professor Jia-qing He, a Chinese botanist who was dedicated to plant investigation in the Dabie Mountains. He walked about 12,684 km and collected nearly 10,000 specimens during a 255-day fieldtrip in the Dabie Mountains, becoming the first person ever to make a comprehensive wild plant investigation of the Dabie Mountains.
Conservation Status:Amana hejiaqingii is distributed in several places in Henan and Hubei provinces, with thousands of individuals at each site, thus we suspect that A. hejiaqingii could be categorized as Least Concern (LC) according to IUCN criteria (IUCN Standards and Petitions Committee, 2022).
Additional specimens examined (paratypes): CHINA. Henan Province: Tongbai County, Huaiyuan Town, Huaiyuan Scenic Area (淮源风景区), 249 m, 7 March 2016, Fr., Fuhe Chen LP161136 (HZU); Tongbai County, Chengjiao Town (城郊乡), 196 m, 24 February 2020, Fl., Fuhe Chen LP207883 (HZU); Tongbai County, Tayuan Temple (塔院寺), 248 m, 8 March 2021, Fr., Pan Li et al. WMZ1489 (HZU); ibidem, 139 m, 14 February 2022, Fl., Pan Li et al. WMZ1711 (HZU); Tongbai County, Yuehe Town, Mt. Bijia (笔架山), 157 m, 8 March 2021, Fr., Pan Li et al. WMZ1492 (HZU); ibidem, 105 m, 14 February 2022, Fl., Pan Li et al. WMZ1712 (HZU); Xinyang City, Shihe District, Heilongtan Waterfall (黑龙潭瀑布), 185 m, 14 February 2022, Fl., Pan Li et al. WMZ1714 (HZU); Shangcheng County, Liluocheng (里罗城), 416 m, 9 April 2017, Fr., Xinglv Xie LP173093 (HZU); ibidem, 7 March 2021, Fr., Pan Li et al. WMZ1483 (HZU). Hubei Province: Guangshui City, Wushengguan Town, Heilongtan Scenic Area (黑龙潭风景区), 529 m, 8 March 2021, Fr., Pan Li et al. WMZ1487 (HZU); ibidem, 371 m, 14 February 2022, Fl., Pan Li et al. WMZ1718 (HZU); Guangshui City, Santan Scenic Area (三潭风景区), 199 m, 14 February 2022, Fl., Pan Li et al. WMZ1716 (HZU).
Key to the Amana:
| 1. Bracts usually two, opposite. | 2 |
| 1. Bracts usually three, verticillate, or not verticillate (in this case degraded). | 3 |
| 2. Lower leaves linear; flowers 1–5; anthers yellow at maturity (before releasing pollens). | Amana edulis |
| 2. Lower leaves oblanceolate; flower mostly solitary, sometimes two; anthers purple at maturity (before releasing pollens). | Amana nanyueensis |
| 3. Bracts usually not verticillate, degraded, 1–5 mm long. | Amana wanzhensis |
| 3. Bracts verticillate, not degraded, longer than 1.2 cm. | 4 |
| 4. Lower leaves linear, or linear to oblanceolate in the same population, always with a broad white band along the midvein above. | 5 |
| 4. Lower leaves oblong or oblanceolate, sometimes with white veins or midvein, but not a broad white band. | 6 |
| 5. Leaves green, linear, 0.4–1 cm wide; purple-red on the back of outer tepals. | Amana baohuaensis |
| 5. Leaves green or brownish-green to purple, linear to oblanceolate, 1–2 cm wide; purple-red streaks on the back of outer tepals. | Amana latifolia |
| 6. Anthers purple at maturity (before releasing pollens). | 7 |
| 6. Anthers yellow at maturity (before releasing pollens). | 8 |
| 7. Leaves green, with several white veins; bulb tunic sparsely villous in-side. | Amana anhuiensis |
| 7. Leaves green, dark-green or purplish-green, without white veins; bulb tunic glabrous inside. | Amana kuocangshanica |
| 8. Leaves oblong; bulb tunic densely villous-woolly inside. | Amana erythronioides |
| 8. Leaves oblanceolate; bulb tunic glabrous or sparely villous inside. | 9 |
| 9. Flowers pink, solitary. | Amana hejiaqingii |
| 9. Flowers white, mostly solitary, sometimes two. | Amana tianmuensis |
Supplementary Materials
The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/taxonomy2030022/s1, Figure S1: The complete plastome circle diagram of Amana hejiaqingii; Table S1: Morphological data of Amana anhuiensis, A. hejiaqingii and A. tianmuensis.
Author Contributions
Conceptualization, P.L.; methodology, P.L.; investigation, P.L., M.W., S.Z., J.W., X.Z., Z.L. and G.L.; experiment, J.W.; writing—original draft preparation, M.W.; writing—review and editing, M.W. and P.L.; supervision, P.L.; funding acquisition, P.L. All authors have read and agreed to the published version of the manuscript.
Funding
The research is supported by the National Natural Science Foundation of China (Grant No. 31970225).
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Data Availability Statement
All DNA sequences used in this study are in GenBank (https://www.ncbi.nlm.nih.gov), accessed on 27 October 2021.
Acknowledgments
We sincerely thank Fuhe Chen for helping with collection, Xin-Jie Jin (Wenzhou University) for colored botanical illustration.
Conflicts of Interest
The authors declare no conflict of interest.
References
- Tan, D.Y.; Zhang, Z.; Li, X.R.; Hong, D.Y. Restoration of the genus Amana Honda (Liliaceae) based on a cladistic analysis of morphological characters. Acta Phytotax. Sin. 2005, 43, 262–270. [Google Scholar] [CrossRef]
- Ohwi, J.; Kitagawa, M. New Flora of Japan; Shibundo Co. Ltd.: Tokyo, Japan, 1992. [Google Scholar]
- Chen, X.Q.; Mordak, H.V. Tulipa Linnaeus. In Flora of China; Wu, Z.-Y., Raven, P.H., Eds.; Science Press: Beijing, China; Missouri Botanical Garden Press: St. Louis, MO, USA, 2000; Volume 24, pp. 123–126. [Google Scholar]
- Shen, X.S. A new species of Tulipa (Liliaceae) from China. Acta Bot. Yunnanica 2001, 23, 39–40. [Google Scholar] [CrossRef] [Green Version]
- Tan, D.Y.; Li, X.R.; Hong, D.Y. Amana kuocangshanica (Liliaceae) a new species from south–east China. Bot. J. Linn. Soc. 2007, 154, 435–442. [Google Scholar] [CrossRef] [Green Version]
- Tan, D.Y.; Li, X.R.; Hong, D.Y. Neotypification and Additional Description of Amana anhuiensis (X.S. Shen) D.Y. Tan & D.Y. Hong (Liliaceae) from Anhui, China. Acta Bot. Boreal. Occid. Sin. 2008, 28, 0393–0395. [Google Scholar]
- Zhang, K.; Huang, L. Amana wanzhensis (Liliaceae), a new species from Anhui, China. Phytotaxa 2014, 177, 118–124. [Google Scholar] [CrossRef] [Green Version]
- Li, P.; Lu, R.S.; Xu, W.Q.; Ohi-Toma, T.; Cai, M.Q.; Qiu, Y.X.; Fu, C.X.; MCameron, K. Comparative genomics and phylogenomics of East Asian Tulips (Amana, Liliaceae). Front. Plant Sci. 2017, 8, 451. [Google Scholar] [CrossRef] [Green Version]
- Wang, L.; Xing, Q.; Lu, G.Y.; Lu, X.; Zhao, Q.; Song, X.W.; Han, B.X. Amana baohuaensis (Liliaceae), a new species from East China. Phytotaxa 2019, 427, 43–50. [Google Scholar] [CrossRef]
- Wang, M.Z.; Fan, X.K.; Zhang, Y.H.; Wu, J.; Mao, L.M.; Zhang, S.L.; Cai, M.Q.; Li, M.H.; Zhu, Z.S.C.; Zhao, M.S.; et al. Phylogenomics and integrative taxonomy reveal two new species of Amana (Liliaceae). Pl. Diversity 2022. [Google Scholar] [CrossRef]
- Struik, G.J. Growth patterns of some native annual and perennial herbs in southern Wisconsin. Ecology 1965, 46, 401–420. [Google Scholar] [CrossRef]
- Wu, J.; Wang, M.Z.; Zhu, Z.S.C.; Cai, M.Q.; Lee, J.; Li, P. Cytogeography of the East Asian Tulips (Amana, Liliaceae). Taxonomy 2022, 2, 145–159. [Google Scholar] [CrossRef]
- Jin, J.J.; Yu, W.B.; Yang, J.B.; Song, Y.; de Pamphilis, C.W.; Yi, T.S.; Li, D.Z. GetOrganelle: A fast and versatile toolkit for accurate de novo assembly of organelle genomes. Genome. Biol. 2020, 21, 241. [Google Scholar] [CrossRef] [PubMed]
- Thiers, B.M.; Tulig, M.C.; Watson, K.A. Digitization of The New York Botanical Garden Herbarium. Brittonia 2016, 68, 324–333. [Google Scholar] [CrossRef]
- Wickham, H. Ggplot2: Elegant Graphics for Data Analysis; Springer: New York, NY, USA, 2016. [Google Scholar]
- Stebbins, G.L. Chromosomal Evolution in Higher Plants; Addison-Wesley: London, UK, 1971; pp. 87–93. [Google Scholar]
- Paszko, B. A critical review and a new proposal of karyotype asymmetry indices. Plant Syst. Evol. 2006, 258, 39–48. [Google Scholar] [CrossRef]
- Peruzzi, L.; Leitch, I.J.; Caparelli, K.F. Chromosome diversity and evolution in Liliaceae. Ann. Bot. 2009, 103, 459–475. [Google Scholar] [CrossRef]
- Peruzzi, L.; Eroğlu, H.E. Karyotype asymmetry: Again, how to measure and what to measure? Comp. Cytogen. 2013, 7, 1–9. [Google Scholar] [CrossRef] [PubMed]
- Peruzzi, L.; Altınordu, F. A proposal for a multivariate quantitative approach to infer karyological relationships among taxa. Comp. Cytogen. 2014, 8, 337. [Google Scholar] [CrossRef]
- Altınordu, F.; Peruzzi, L.; Yu, Y.; He, X.J. A tool for the analysis of chromosomes: KaryoType. Taxon 2016, 65, 586–592. [Google Scholar] [CrossRef]
- Lu, R.S.; Yang, T.; Chen, Y.; Wang, S.Y.; Cai, M.Q.; MCameron, K.; Li, P.; Fu, C.X. Comparative plastome genomics and phylogenetic analyses of Liliaceae. Bot. J. Linn. Soc. 2021, 196, 279–293. [Google Scholar] [CrossRef]
- Kearse, M.; Moir, R.; Wilson, A.; Stones-Havas, S.; Cheung, M.; Sturrock, S.; Buxton, S.; Cooper, A.; Markowitz, S.; Duran, C.; et al. Geneious Basic: An integrated and extendable desktop software platform for the organization and analysis of sequence data. Bioinformatics 2012, 28, 1647–1649. [Google Scholar] [CrossRef]
- Minh, B.Q.; Schmidt, H.A.; Chernomor, O.; Schrempf, D.; Woodhams, M.D.; von Haeseler, A.; Lanfear, R. IQ-TREE 2: New models and efficient methods for phylogenetic inference in the genomic era. Mol. Biol. Evol. 2020, 37, 1530–1534. [Google Scholar] [CrossRef] [Green Version]
- Kalyaanamoorthy, S.; Minh, B.Q.; Wong, T.K.F.; Haeseler Av Jermiin, L.S. ModelFinder: Fast model selection for accurate phylogenetic estimates. Nat. Methods 2017, 14, 587–589. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Ronquist, F.; Huelsenbeck, J.P. MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics 2003, 19, 1572–1574. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Figure 1.
Distribution of Amana hejiaqingii. The red dots represent the known populations of Amana hejiaqingii.
Figure 1.
Distribution of Amana hejiaqingii. The red dots represent the known populations of Amana hejiaqingii.
Figure 2.
(A–J) Amana hejiaqingii: (A) Habitat, (B) Individual, (C) Population with fruits, (D) Whole plant, (E) The front view of the flower, (F) The side view of the flower, (G) Anatomy of flower, (H) Bulb, (I) Leaves, (J) Fruits. The white line segment represents a length of 1 cm.
Figure 2.
(A–J) Amana hejiaqingii: (A) Habitat, (B) Individual, (C) Population with fruits, (D) Whole plant, (E) The front view of the flower, (F) The side view of the flower, (G) Anatomy of flower, (H) Bulb, (I) Leaves, (J) Fruits. The white line segment represents a length of 1 cm.
Figure 3.
Illustration of Amana hejiaqingii (A1,A2) Flowering plants, (B1) Flower, (B2) Abaxial surface of outer tepal, (B3) Abaxial surface of inner tepal, (B4) Adaxial surface of outer tepal, (B5) Adaxial surface of inner tepal, (B6) Outer stamen, (B7) Inner stamen, (C1) Fruit, (C2) Longitudinal section of ovary, (C3) Immature capsule and bracts, (C4) Transverse section of ovary, (C5) Seed, (D) Bulb. Drawn by Xin-Jie Jin.
Figure 3.
Illustration of Amana hejiaqingii (A1,A2) Flowering plants, (B1) Flower, (B2) Abaxial surface of outer tepal, (B3) Abaxial surface of inner tepal, (B4) Adaxial surface of outer tepal, (B5) Adaxial surface of inner tepal, (B6) Outer stamen, (B7) Inner stamen, (C1) Fruit, (C2) Longitudinal section of ovary, (C3) Immature capsule and bracts, (C4) Transverse section of ovary, (C5) Seed, (D) Bulb. Drawn by Xin-Jie Jin.
Figure 4.
(A–J) Amana anhuiensis: (A) Habitat, (B) Population with flowers, (C) Population with fruits, (D) Whole plant, (E) The front view of the flower, (F) The side view of the flower, (G) Anatomy of flower, (H) Bulb, (I) Leaves, (J) Fruits. The white line segment represents a length of 1 cm.
Figure 4.
(A–J) Amana anhuiensis: (A) Habitat, (B) Population with flowers, (C) Population with fruits, (D) Whole plant, (E) The front view of the flower, (F) The side view of the flower, (G) Anatomy of flower, (H) Bulb, (I) Leaves, (J) Fruits. The white line segment represents a length of 1 cm.
Figure 5.
Principal coordinates analysis plot of Amana anhuiensis, Amana hejiaqingii and Amana tianmuensis. The ellipse represents the 95% confidence interval.
Figure 5.
Principal coordinates analysis plot of Amana anhuiensis, Amana hejiaqingii and Amana tianmuensis. The ellipse represents the 95% confidence interval.
Figure 6.
Chromosome number of Amana hejiaqingii (2n = 2x = 24).
Figure 7.
Phylogenetic tree of Amana based on plastid CDS sequences. All branches have Bayesian inference posterior probability (BIPP) =1.0. The numbers on the tree represent maximum likelihood bootstrap (MLBS) values. The unmarked branches all have BIPP = 1.0, MLBS = 100%.
Figure 7.
Phylogenetic tree of Amana based on plastid CDS sequences. All branches have Bayesian inference posterior probability (BIPP) =1.0. The numbers on the tree represent maximum likelihood bootstrap (MLBS) values. The unmarked branches all have BIPP = 1.0, MLBS = 100%.
Table 1.
The plastome sequences of Amana accessions used in this research.
| Accession Name | Accession Number | Location |
|---|---|---|
| Amana anhuiensis_CMQ2015075-7 | KY401423 | Tianzhushan, Qianshan County, Anhui Province, China |
| Amana anhuiensis_LJK62-1 | MZ561649 | Tianzhushan, Qianshan County, Anhui Province, China |
| Amana baohuaensis_ LP150012 | MW929176 | Maoshan, Jurong City, Jiangsu Province, China |
| Amana baohuaensis_LJK31-1 | MZ561647 | Maoshan, Jurong City, Jiangsu Province, China |
| Amana hejiaqingii_WMZ1483 | ON764433 | Liluocheng, Shangcheng County, Xinyang City, Henan Province, China |
| Amana hejiaqingii_WMZ1495 | ON764434 | Feiyundong, Xisaishan District, Huangshi City, Hubei Province, China |
| Amana edulis_CMQ16213 | OL351567 | Xilin Temple, Jiujiang City, Jiangxi Province, China |
| Amana edulis_LJK54-1 | MW929177 | Yuxiang Village, Huangshan City, Anhui Province, China |
| Amana edulis_LP161115-1 | AB024388 | Hangzhou Botanical Garden, Hangzhou City, Zhejiang Province, China |
| Amana edulis_LP161235-1 | MW938051 | Daheishan, Dalian City, Liaoning Province, China |
| Amana edulis_LP173029 | OL351568 | Cheyu Valley, Zhouzhi County, Shaanxi Province, China |
| Amana edulis_LP173055 | OL351569 | Dushan, Nanyang City, Henan Province, China |
| Amana erythronioides_LP150068-4 | KY401421 | Simingshan, Yuyao City, Zhejiang Province, China |
| Amana erythronioides_LJK26-1 | MZ561646 | Simingshan, Yuyao City, Zhejiang Province, China |
| Amana kuocangshanica_PNLI20141039-1 | KY401426 | Kuocangshan, Linhai City, Zhejiang Province, China |
| Amana kuocangshanica_LJK22-1 | MZ561645 | Kuocangshan, Linhai City, Zhejiang Province, China |
| Amana latifolia_LJK70-1 | MZ561650 | Koshikawa Botanical Garden, Tokyo, Japan |
| Amana latifolia_LP161225-2 | KY401424 | Koishikawa Botanical Garden, Tokyo, Japan |
| Amana nanyueensis_LP173011-2 | MW876380 | Hengshan, Hengyang City, Huan Province, China |
| Amana nanyueensis_LP196219-1 | MW845753 | Hengshan, Hengyang City, Huan Province, China |
| Amana tianmuensis_LP161203-2 | MW876379 | Jinhuashan, Jinhua City, Zhejiang Province, China |
| Amana tianmuensis_LJK42-1 | MW876378 | Tianmushan, Lin’an City, Zhejiang Province, China |
| Amana tianmuensis_CMQ16198-1 | MW876377 | Tianmushan, Lin’an City, Zhejiang Province, China |
| Amana wanzhensis_LJK44-1 | MZ561648 | Xianxia Town, Ningguo City, Anhui Province, China |
| Amana wanzhensis_LP150072-11 | KY401422 | Xianxia Town, Ningguo City, Anhui Province, China |
| Erythronium sibiricum | NC_035681 | Xinjiang Province, China |
| Lloydia tibetica | MK673748 | Taibaishan, Mei County, Shaanxi Province, China |
| Tulipa altaica | NC_044780 | Tacheng, Urumqi, Xinjiang Province, China |
Table 2.
Comparison of characteristics between Amana anhuiensis, Amana hejiaqingii and Amana tianmuensis (values in parentheses are averages).
Table 2.
Comparison of characteristics between Amana anhuiensis, Amana hejiaqingii and Amana tianmuensis (values in parentheses are averages).
| Species | Amana anhuiensis | Amana hejiaqingii | Amana tianmuensis | |
|---|---|---|---|---|
| Characters | ||||
| Bulbs | Diameter | 1.13–1.72 cm | 0.93–2.3 cm | 0.7–1.8 cm |
| Tunics | yellowish-brown, thinly papery | yellowish-brown, thinly papery | yellowish-brown, thinly papery | |
| Inside | sparely villous | glabrous, sometimes sparely villous | glabrous, sometimes sparely villous | |
| Leaves | Color | green, with white veins | green, midvein grayish white | green |
| Shape | oblanceolate | oblanceolate | oblanceolate | |
| Lower-leaf length (LL) | 12.2–22.5 (17.05) cm | 8.0–33.9 (19.91) cm | 11.2–22.8 (16.5) cm | |
| Lower-leaf width (LW) | 1.7–2.6 (2.17) cm | 1.0–2.8 (1.71) cm | 0.9–2.5 (1.7) cm | |
| LL/LW | 5.5 < X < 10 | 6 < X < 20 | 5 < X < 14.5 | |
| Upper-leaf length (LL) | 11.0–21.4 (16.05) cm | 7.7–34 (19.47) cm | 9.5–23.4 (16.1) cm | |
| Upper-leaf width (LW) | 0.7–1.85 (1.16) cm | 0.5–1.4 (0.97) cm | 0.6–1.9 (1.2) cm | |
| LL/LW | 10 < X < 20 | 9 < X < 29.5 | 6.5 < X < 21 | |
| Bracts | 3, verticillate, narrowly lanceolate | 3, verticillate, linear | 3, verticillate, linear | |
| Bracts length | 2.8–4.7 (3.5) cm | 1.2–4.2 (2.6) cm | 1.8–3.5 (2.6) cm | |
| Pedicels | 2.2–5.1 cm | 0.5–4.1 cm | 1.1–5.6 cm | |
| Flowers | solitary; white or pink | solitary; pink | mostly solitary, sometimes two; white | |
| Tepals | Outer length | 2.9–4.3 (3.4) cm | 2.4–4.4 (3.4) cm | 1.8–3.4 (2.6) cm |
| Outer width | 0.4–0.6 (0.5) cm | 0.6–1.1 (0.8) cm | 0.4–0.9 (0.5) cm | |
| Inner length | 2.7–4.3 (3.3) cm | 2.1–3.9 (3.2) cm | 1.8–3.2 (2.4) cm | |
| Inner width | 0.7–1.2 (0.9) cm | 0.6–1.0 (0.8) cm | 0.4–1.1 (0.6) cm | |
| Anthers | light-purple | yellow | yellow | |
| Styles | 0.5–0.7 cm long | 0.4–0.6 cm long | 0.5–0.6 cm long | |
| Length of fruit beak | 0.5–1.0 cm long | 0.5–1.2 cm long | 0.45–1.1 cm long | |
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MDPI and ACS Style
Wang, M.; Zhang, S.; Wu, J.; Zhu, X.; Liu, Z.; Lu, G.; Li, P. Amana hejiaqingii (Liliaceae), a New Species from the Dabie Mountains, China. Taxonomy 2022, 2, 279-290. https://doi.org/10.3390/taxonomy2030022
AMA Style
Wang M, Zhang S, Wu J, Zhu X, Liu Z, Lu G, Li P. Amana hejiaqingii (Liliaceae), a New Species from the Dabie Mountains, China. Taxonomy. 2022; 2(3):279-290. https://doi.org/10.3390/taxonomy2030022
Chicago/Turabian StyleWang, Meizhen, Shenglu Zhang, Jing Wu, Xinxin Zhu, Zongcai Liu, Gengyu Lu, and Pan Li. 2022. "Amana hejiaqingii (Liliaceae), a New Species from the Dabie Mountains, China" Taxonomy 2, no. 3: 279-290. https://doi.org/10.3390/taxonomy2030022
