Abstract
Hamamelidales Griseb. (1854) order serves as a foundational group and plays a significant role in the research of evolutionary systematics of the class Rosopsida Batsch (1802) of Fructophyta D. L. Fu & H. Fu (2018). To address the ambiguities surrounding the circumscription of certain genera within this order, such as Paeonia L. (1753), Liquidambar L. (1753), and Hamamelis L. (1753), relevant chloroplast complete genome sequences from the NCBI database were retrieved, and evolutionary analyses were conducted on these sequences in this study. Notably, Lobidiscus D. L. Fu, gen. nov., a new genus endemic to America characterized by its distinctly lobed floral discs, has been separated from Paeonia L. belonging to Paeoniaceae (Bercht. & J. Presl) Rudolphi, nom. cons. (1830), and Lobidiscus californicus (Nutt.) D. L. Fu is designated as its type species. This new genus derives from Moutan Rchb. (1827), rather than Paeonia L., given that a maximum PHS value of 0.837 were observed between Lobidiscus brownii (Hook.) D. L. Fu and Moutan delavayi (Franch.) D. L. Fu based on CPCG evolutionary analyses. Meanwhile, the application of the minimum criterion PHS ≤ 0.928 (intergeneric, CPCG) for genus classification of Fructophyta D. L. Fu & H. Fu, has led to confirmation of two synonyms for Liquidambar L.: Altingia Noronha and Semiliquidambar H. T. Chang; additionally, three current synonyms for Hamamelis L., including Distylium Siebold & Zucc., Parrotia C. A. Mey., and Sycopsis Oliv., have been scientifically identified. In total, 13 novel family names like Liquidambaraceae D. L. Fu, Dianthaceae D. L. Fu, Diospyraceae D. L. Fu and Ilecaceae D. L. Fu have been established, along with two new specific epithets, Hamamelis hubeiensis D. L. Fu and Hamamelis grandifolia D. L. Fu, and 39 newly valid combinations involving Hamamelis L., Liquidambar L., Lobidiscus D. L. Fu, and Moutan Rchb. also been published, such as Hamamelis annamica (Gagnep.) D. L. Fu, Liquidambar cambodiana (Lecomte) D. L. Fu, Lobidiscus brownii (Hook.) D. L. Fu, and Moutan suffruticosus (Andrews) D. L. Fu. These contributions will effectively clarify taxonomic nomenclature confusions in a scientific manner while establishing a robust foundation for further research into the evolutionary systems within the order Hamamelidales Griseb.
Keywords
Lobidiscus, Moutan, Liquidambar, Hamamelis, New Genus, New Combination, CPCG (Chloroplast Complete Genome), Genus Minimum Criterion, Typical Algorithm
1. Introduction
The order Hamamelidales Griseb. (1854) is foundational and plays a significant role in the research of evolutionary systematics of the class Rosopsida Batsch (1802) of Fructophyta D. L. Fu & H. Fu (2018). This order encompasses families such as Hamamelidaceae R. Br., nom. cons. (1818), Vitaceae Juss., nom. cons. (1789), Penthoraceae Rydb. ex Britt., nom. cons. (1901) and Paeoniaceae (Bercht. & J. Presl) Rudolphi, nom. cons. (1830)
[1] | Fu, D. L. An evolutionary particularity principle for evolutionary system of classes of Fructophyta. Amer. J. Agric. Forest. 2019, 7(5): 191-199. https://doi.org/10.11648/j.ajaf.20190705.15 |
[2] | Fu, D. L. The theory and practice of evolutionomy. Beijing: China Forestry Publishing House; 2020, 1-158. |
[1, 2]
. However, traditional taxonomy and modern phylogenetic approaches reveal persistent taxonomic challenges
[3] | Fu, D. L., Fu, H. An evolutionary continuity principle for evolutionary system of organism divisions. Amer. J. Agric. Forest. 2018, 6(3), 25-29. https://doi.org/10.11648/j.ajaf.20180603.14 |
[4] | Fu, D. L., Fu, H., Qin, Y., Zhou, D. S., Duan, R. M. Analyses of chloroplast genomic and morphological evolutionomy of Yulania subsect. Cylindricae (Magnoliaceae). Amer. J. Agric. Forest. 2019, 7(5), 200-211. https://doi.org/10.11648/j.ajaf.20190705.16 |
[5] | Fu, D. L., Fu, H., Duan, R. M., Qin, Y. Evolutionary System of Magnoliaceae Based on Chloroplast Genomic and Morphological Evolutionomy. Amer. J. Agric. Forest. 2024, 12(1), 22-50. https://doi.org/10.11648/j.ajaf.20241201.14 |
[6] | Fu, D. L., Fu, H. New Names and New Combinations of Phyllostachys Sieb. & Zucc. (Bambusaceae). Amer. J. Agric. Forest. 2024, 12(2), 87-106. https://doi.org/10.11648/j.ajaf.20241202.14 |
[7] | Fu, D. L. New Names and New Combinations of the Genera of Bambusa, Dinochloa and Guadua (Bambusaceae). Amer. J. Agric. Forest. 2024, 12(3), 174-184. https://doi.org/10.11648/j.ajaf.20241203.14 |
[8] | Fu, D. L. New Names and New Combinations of Jarava, Cinna, Coleanthus, Sclerochloa and Graphephorum (Poales). Amer. J. Agric. Forest. 2024, 12(4), 242-259. https://doi.org/10.11648/j.ajaf.20241204.13 |
[9] | Fu, D. L. New Names and New Combinations of some genera of Aegilopaceae and Andropogonaceae (Scutellopsida). Amer. J. Agric. Forest. 2024, 12(4), 289-306. https://doi.org/10.11648/j.ajaf.20241204.17 |
[3-9]
, particularly regarding ambiguities in the circumscription of certain genera including
Paeonia L. (1753),
Liquidambar L. (1753), and
Hamamelis L. (1753) within this order.
In 1804, the species of Mudan, renowned as the "King of Flowers" in China, was officially published and named
Paeonia suffruticosa Andrews (Woody Peony). This was also the first species of
Moutan taxa to be released, in accordance with the relevant articles of the International Code of Botanical Nomenclature, the name holds absolute precedence in the names of
Moutan taxa. Consequently, the assertion that “many scholars have confirmed that
P. suffruticosa is a hybrid formed by repeated hybridization of several species of subsect.
Vaginatae, based on morphological and molecular biological evidence”
[10] | Yang, Y., Sun, M., Li, S. S., Chen, Q. H., Silva, J. A. T., Wang, A. J., Yu X. N., Wang L. S. Germplasm resources and genetic breeding of Paeonia: a systematic review. Hort. Res. 2020, 7: 107. https://doi.org/10.1038/s41438-020-0332-2 |
[10]
is wholly incorrect. In other words, as long as the type of
P. suffruticosa is authentic, regardless of whether it is collected from cultivated or wild plants, the species must be acknowledged. It implies that all other subsequent species of
Moutan taxa can be regarded as the hybrids (alternative forms of varieties) of
P. suffruticosa, yet
P. suffruticosa cannot be considered as a hybrid of these later species. In 1824, the
Paeonia sect.
Moutan DC. was published
[11] | AASE (Agendae Academiae Sinicae Edita). Flora Reipublicae Popularis Sinicae. Beijing: Science Press; 1979, vol. 27, pp. 37-59. |
[11]
, and in 1827, the genus
Moutan Rchb. was established. This was a typical course of development in plant taxonomy; however, it failed to draw the attention of taxonomists, despite the
Moutan taxa having very distinct characteristics, such as the woody stems and the envelope discs
[11] | AASE (Agendae Academiae Sinicae Edita). Flora Reipublicae Popularis Sinicae. Beijing: Science Press; 1979, vol. 27, pp. 37-59. |
[12] | Hong, T., Zhang, J. X., Li, J. J., Zhao, W. Z., Li, M. R. Study on the Chinese wild woody peonies (1): new taxa of Paeonia L. sect. Moutan DC. Bull. Bot. Res. 1992, 12, 223–234. |
[13] | Hong, T., Osti, G. L. Study on the Chinese wild woody peonies (II): new taxa of Paeonia L. sect. Moutan DC. Bull. Bot. Res. 1994, 14, 237–240. |
[14] | Hong, T., Dai, Z. L. Study on the Chinese wild woody Peonies (III): new taxa of Paeonia L. sect. Moutan DC. Bull. Bot. Res. 1997, 17, 1–5. |
[15] | Pei, Y. L., Hong, D. Y. Paeonia qiui – a new woody species of Paeonia from Hubei, China. Acta Phytotax. Sin. 1995, 33, 91–93. |
[16] | Hong, D. Y. Paeonia (Paeoniaceae) in Xizang (Tibet). Novon 1997, 7, 156–161. |
[17] | Hong, D. Y. Paeonia rockii and its one new subspecies from Mt. Taibai, Shanxi of China. Acta Phytotax. Sin. 1998, 36(6), 538–543. |
[18] | Hong, D. Y., Pan, K. Y. Paeonia cathayana, a new tree peony, with revision of P. suffruticosa subsp. yinpingmudan. Acta Phytotax. Sin. 2007, 45, 285–288. https://doi.org/10.1360/aps07043 |
[19] | Hong, D. Y. Peonies of the world: taxonomy and phytogeography. London: Royal Botanical Garden, Kew; 2010. |
[11-19]
. Subsequently, species within the
Moutan taxa such as
Paeonia delavayi Franch (1887),
Paeonia potaninii Komarov (1921), and
Paeonia decomposita Hand-Mazz. (1939), have continued to utilize the genus name
Paeonia L. Over the past three decades, Chinese
Moutan taxonomist Hong T.
[12] | Hong, T., Zhang, J. X., Li, J. J., Zhao, W. Z., Li, M. R. Study on the Chinese wild woody peonies (1): new taxa of Paeonia L. sect. Moutan DC. Bull. Bot. Res. 1992, 12, 223–234. |
[13] | Hong, T., Osti, G. L. Study on the Chinese wild woody peonies (II): new taxa of Paeonia L. sect. Moutan DC. Bull. Bot. Res. 1994, 14, 237–240. |
[14] | Hong, T., Dai, Z. L. Study on the Chinese wild woody Peonies (III): new taxa of Paeonia L. sect. Moutan DC. Bull. Bot. Res. 1997, 17, 1–5. |
[12-14]
and world-renowned
Paeonia taxonomist Hong D. Y.
[15] | Pei, Y. L., Hong, D. Y. Paeonia qiui – a new woody species of Paeonia from Hubei, China. Acta Phytotax. Sin. 1995, 33, 91–93. |
[16] | Hong, D. Y. Paeonia (Paeoniaceae) in Xizang (Tibet). Novon 1997, 7, 156–161. |
[17] | Hong, D. Y. Paeonia rockii and its one new subspecies from Mt. Taibai, Shanxi of China. Acta Phytotax. Sin. 1998, 36(6), 538–543. |
[18] | Hong, D. Y., Pan, K. Y. Paeonia cathayana, a new tree peony, with revision of P. suffruticosa subsp. yinpingmudan. Acta Phytotax. Sin. 2007, 45, 285–288. https://doi.org/10.1360/aps07043 |
[19] | Hong, D. Y. Peonies of the world: taxonomy and phytogeography. London: Royal Botanical Garden, Kew; 2010. |
[15-19]
have also maintained the use of the genus name in their publications concerning
Moutan taxa. However, contemporary phylogenic studies
[20] | Sang, T., Crawford, D. J., Stuessy, T. F. Chloroplast DNA Phylogeny, Reticulate Evolution, and Biogeography of Paeonia (Paeoniaceae). Amer. J. Bot. 1997, 84(9), 1120–1136. https://doi.org/10.2307/2446155 |
[21] | Wu, L. W., Nie, L. P., Wang, Q., Xu, Z. C., Wang, Y., He, C. N., Song, J. Y., Yao, H. Comparative and phylogenetic analyses of the chloroplast genomes of species of Paeoniaceae. Sci. Rep. 2021, 11, 14643. https://doi.org/10.1038/s41598-021-94137-0 |
[20-21]
have demonstrated that the genus
Paeonia L. can be clearly divided into three distinct taxa, now recognized as 3 subgenera or 3 sections. Further investigations are requisite to ascertain whether these two additional taxa may warrant classification as separate genera based on their unique taxonomic characteristics
[12] | Hong, T., Zhang, J. X., Li, J. J., Zhao, W. Z., Li, M. R. Study on the Chinese wild woody peonies (1): new taxa of Paeonia L. sect. Moutan DC. Bull. Bot. Res. 1992, 12, 223–234. |
[13] | Hong, T., Osti, G. L. Study on the Chinese wild woody peonies (II): new taxa of Paeonia L. sect. Moutan DC. Bull. Bot. Res. 1994, 14, 237–240. |
[14] | Hong, T., Dai, Z. L. Study on the Chinese wild woody Peonies (III): new taxa of Paeonia L. sect. Moutan DC. Bull. Bot. Res. 1997, 17, 1–5. |
[15] | Pei, Y. L., Hong, D. Y. Paeonia qiui – a new woody species of Paeonia from Hubei, China. Acta Phytotax. Sin. 1995, 33, 91–93. |
[16] | Hong, D. Y. Paeonia (Paeoniaceae) in Xizang (Tibet). Novon 1997, 7, 156–161. |
[17] | Hong, D. Y. Paeonia rockii and its one new subspecies from Mt. Taibai, Shanxi of China. Acta Phytotax. Sin. 1998, 36(6), 538–543. |
[18] | Hong, D. Y., Pan, K. Y. Paeonia cathayana, a new tree peony, with revision of P. suffruticosa subsp. yinpingmudan. Acta Phytotax. Sin. 2007, 45, 285–288. https://doi.org/10.1360/aps07043 |
[19] | Hong, D. Y. Peonies of the world: taxonomy and phytogeography. London: Royal Botanical Garden, Kew; 2010. |
[22] | Bernhardt, P., Meier, R., Vance, N. Pollination ecology and floral functions of Brown's peony (Paeonia brownii) in the Blue Mountains of northeastern Oregon. J. Poll. Ecol. 2013, 11(2), 9-20. https://doi.org/10.26786/1920-7603(2013)2 |
[12-19, 22]
.
In another instance, phylogenic analyses have revealed that
Altingia Noronha and
Semiliquidambar H. T. Chang are nested within
Liquidambar L., leading to the formal transfer of all
Altingia and
Semiliquidambar species to
Liquidambar L.
[23] | Ickert-Bond, S. M., Wen, J. Phylogeny and biogeography of Altingiaceae: Evidence from combined analysis of five non-coding chloroplast regions. Mol. Phyl. Evol. 2006, 39, 512–528. https://doi.org/10.1016/j.ympev.2005.12.003 |
[24] | Ickert-Bond, S. M., Pigg, K. B., Wen, J. Comparative Infructescence Morphology in Altingia (Altingiaceae) and Discordance between Morphological and Molecular Phylogenies. Amer. J. Bot. 2007, 94(7), 1094–1115. https://doi.org/10.3732/ajb.94.7.1094 |
[25] | Ickert-Bond, S. M., Wen, J. A taxonomic synopsis of Altingiaceae with nine new combinations. PhytoKeys 2013, 31: 21–61. https://doi.org/10.3897/phytokeys.31.6251 |
[23-25]
. The reasons for this nesting typically involve the synonymy of
Altingia and
Semiliquidambar with
Liquidambar L., or the characterization of
Liquidambar L. as a diverse genus, with exceptions arising from sampling and analysis errors. Consequently, further analyses are warranted to ascertain whether the other two genera should be considered synonyms of
Liquidambar L.
Similarly, phylogenetic analyses have indicated a close relationship between the genus
Hamamelis L. and
Distylium Siebold & Zucc.,
Parrotia C. A. Mey., and
Sycopsis Oliv.
[26] | Wang, N. J., Chen, S. F., Xie, L., Wang, L., Feng, Y. Y., Lv, T., Fang, Y. M., Ding, H. The complete chloroplast genomes of three Hamamelidaceae species: Comparative and phylogenetic analyses. Ecol. Evol. 2022, 12, e8637. https://doi.org/10.1002/ece3.8637 |
[27] | Jin, Z. C., Xu, L. S., Xu, Y. C., Chen, Y. S. Loropetalum axillare (Hamamelidaceae), a new species from Guangdong, China. Phytotaxa 2023, 622(1), 085–094. https://doi.org/10.11646/phytotaxa.622.1.6 |
[26, 27]
, some of which are nested. Therefore, further analyses are required to determine whether the other three genera should be considered synonyms of
Hamamelis L. or if
Distylium Sieb. & Zucc. represents a diverse genus.
Both traditional taxonomy and modern phylogeny encounter limitations in their objectivity and impartiality when it comes to determine whether a genus is the synonym or a diverse genus. The new science evolutionomy has been developed with the publications of the evolutionary continuity principle, the evolutionary particularity principle, the theoretical monograph as
the Theory and Practice of Evolutionomy, and so on
[1] | Fu, D. L. An evolutionary particularity principle for evolutionary system of classes of Fructophyta. Amer. J. Agric. Forest. 2019, 7(5): 191-199. https://doi.org/10.11648/j.ajaf.20190705.15 |
[2] | Fu, D. L. The theory and practice of evolutionomy. Beijing: China Forestry Publishing House; 2020, 1-158. |
[3] | Fu, D. L., Fu, H. An evolutionary continuity principle for evolutionary system of organism divisions. Amer. J. Agric. Forest. 2018, 6(3), 25-29. https://doi.org/10.11648/j.ajaf.20180603.14 |
[4] | Fu, D. L., Fu, H., Qin, Y., Zhou, D. S., Duan, R. M. Analyses of chloroplast genomic and morphological evolutionomy of Yulania subsect. Cylindricae (Magnoliaceae). Amer. J. Agric. Forest. 2019, 7(5), 200-211. https://doi.org/10.11648/j.ajaf.20190705.16 |
[5] | Fu, D. L., Fu, H., Duan, R. M., Qin, Y. Evolutionary System of Magnoliaceae Based on Chloroplast Genomic and Morphological Evolutionomy. Amer. J. Agric. Forest. 2024, 12(1), 22-50. https://doi.org/10.11648/j.ajaf.20241201.14 |
[6] | Fu, D. L., Fu, H. New Names and New Combinations of Phyllostachys Sieb. & Zucc. (Bambusaceae). Amer. J. Agric. Forest. 2024, 12(2), 87-106. https://doi.org/10.11648/j.ajaf.20241202.14 |
[7] | Fu, D. L. New Names and New Combinations of the Genera of Bambusa, Dinochloa and Guadua (Bambusaceae). Amer. J. Agric. Forest. 2024, 12(3), 174-184. https://doi.org/10.11648/j.ajaf.20241203.14 |
[8] | Fu, D. L. New Names and New Combinations of Jarava, Cinna, Coleanthus, Sclerochloa and Graphephorum (Poales). Amer. J. Agric. Forest. 2024, 12(4), 242-259. https://doi.org/10.11648/j.ajaf.20241204.13 |
[9] | Fu, D. L. New Names and New Combinations of some genera of Aegilopaceae and Andropogonaceae (Scutellopsida). Amer. J. Agric. Forest. 2024, 12(4), 289-306. https://doi.org/10.11648/j.ajaf.20241204.17 |
[1-9]
. The establishment, publication, and implementation of the minimum criterion PHS ≤ 0.928 (intergeneric, CPCG) for the classification of genus of Fructophyta D. L. Fu & H. Fu has scientifically identified 107 current genus synonyms within the class Scutellopsida D. L. Fu, and the taxonomic confusions of the class has also been scientifically resolved to a certain extent.
[4] | Fu, D. L., Fu, H., Qin, Y., Zhou, D. S., Duan, R. M. Analyses of chloroplast genomic and morphological evolutionomy of Yulania subsect. Cylindricae (Magnoliaceae). Amer. J. Agric. Forest. 2019, 7(5), 200-211. https://doi.org/10.11648/j.ajaf.20190705.16 |
[5] | Fu, D. L., Fu, H., Duan, R. M., Qin, Y. Evolutionary System of Magnoliaceae Based on Chloroplast Genomic and Morphological Evolutionomy. Amer. J. Agric. Forest. 2024, 12(1), 22-50. https://doi.org/10.11648/j.ajaf.20241201.14 |
[6] | Fu, D. L., Fu, H. New Names and New Combinations of Phyllostachys Sieb. & Zucc. (Bambusaceae). Amer. J. Agric. Forest. 2024, 12(2), 87-106. https://doi.org/10.11648/j.ajaf.20241202.14 |
[7] | Fu, D. L. New Names and New Combinations of the Genera of Bambusa, Dinochloa and Guadua (Bambusaceae). Amer. J. Agric. Forest. 2024, 12(3), 174-184. https://doi.org/10.11648/j.ajaf.20241203.14 |
[8] | Fu, D. L. New Names and New Combinations of Jarava, Cinna, Coleanthus, Sclerochloa and Graphephorum (Poales). Amer. J. Agric. Forest. 2024, 12(4), 242-259. https://doi.org/10.11648/j.ajaf.20241204.13 |
[9] | Fu, D. L. New Names and New Combinations of some genera of Aegilopaceae and Andropogonaceae (Scutellopsida). Amer. J. Agric. Forest. 2024, 12(4), 289-306. https://doi.org/10.11648/j.ajaf.20241204.17 |
[4-9]
.
To scientifically identify the circumscription of certain genera and resolve the synonyms or diverse genera leading to the taxonomic confusions within the three genera of Hamamelidales Griseb., some relevant CPCG sequences from the NCBI (National Center for Biotechnology Information, USA) database have been downloaded and the evolutionary analyses on these sequences have been conducted, and the results are as follows.
2. Materials and Methods
2.1. CPCG of Hamamelidales
Total 28 CPCG of representative species of three families of Hamamelidales Griseb. were selected from the NCBI database. Their current names, scientific names and CPCG numbers of NCBI are listed in
Table 1 to
Table 6.
2.2. Evolutionary Analyses of CPCG
The evolutionary analyses of CPCG mainly use the typical algorithm
[3] | Fu, D. L., Fu, H. An evolutionary continuity principle for evolutionary system of organism divisions. Amer. J. Agric. Forest. 2018, 6(3), 25-29. https://doi.org/10.11648/j.ajaf.20180603.14 |
[4] | Fu, D. L., Fu, H., Qin, Y., Zhou, D. S., Duan, R. M. Analyses of chloroplast genomic and morphological evolutionomy of Yulania subsect. Cylindricae (Magnoliaceae). Amer. J. Agric. Forest. 2019, 7(5), 200-211. https://doi.org/10.11648/j.ajaf.20190705.16 |
[5] | Fu, D. L., Fu, H., Duan, R. M., Qin, Y. Evolutionary System of Magnoliaceae Based on Chloroplast Genomic and Morphological Evolutionomy. Amer. J. Agric. Forest. 2024, 12(1), 22-50. https://doi.org/10.11648/j.ajaf.20241201.14 |
[6] | Fu, D. L., Fu, H. New Names and New Combinations of Phyllostachys Sieb. & Zucc. (Bambusaceae). Amer. J. Agric. Forest. 2024, 12(2), 87-106. https://doi.org/10.11648/j.ajaf.20241202.14 |
[7] | Fu, D. L. New Names and New Combinations of the Genera of Bambusa, Dinochloa and Guadua (Bambusaceae). Amer. J. Agric. Forest. 2024, 12(3), 174-184. https://doi.org/10.11648/j.ajaf.20241203.14 |
[8] | Fu, D. L. New Names and New Combinations of Jarava, Cinna, Coleanthus, Sclerochloa and Graphephorum (Poales). Amer. J. Agric. Forest. 2024, 12(4), 242-259. https://doi.org/10.11648/j.ajaf.20241204.13 |
[9] | Fu, D. L. New Names and New Combinations of some genera of Aegilopaceae and Andropogonaceae (Scutellopsida). Amer. J. Agric. Forest. 2024, 12(4), 289-306. https://doi.org/10.11648/j.ajaf.20241204.17 |
[3-9]
to determine the relative evolutionary relationships between different taxa by comparing the phylogenetic similarity (PHS) between the designated type and target taxa. The formula is as follows:
PHS = phylogenetic similarity between the type and objective taxon; SPHL = the number of same phylogenetic loci between the type and objective taxon; APHL = the number of all phylogenetic loci of the type; statistics of phylogenetic loci using Nucleotide Barcodes (17bp).
3. Results
3.1. Evolutionary System of Paeoniaceae
Using the types of
Moutan suffruticosus (Andrews) D. L. Fu,
Paeonia lactiflora Pall.,
Lobidiscus brownii (Hook.) D. L. Fu, and
Cercidiphyllum japonicum Siebold & Zucc. respectively, the PHS of CPCG of total 17 species, 16 species of Paeoniaceae and
Cercidiphyllum japonicum Siebold & Zucc. are analyzed, and the results are shown in
Table 1 to
Table 4.
Table 1. PHS of CPCG between Moutan suffruticosus and some representative species of Paeoniaceae.
No. | Scientific Names and Numbers of CPCG in NCBI | Current Names | PHL/17bp | PHS |
1 | Moutan suffruticosus_JQ952559.1 | Paeonia suffruticosa | 127105 | 1 |
2 | Moutan ostii_MK701990.1 | Paeonia ostii | 122827 | 0.966 |
3 | Moutan qiui_MT210544.1 | Paeonia qiui | 122471 | 0.964 |
4 | Moutan decompositus_NC039425.1 | Paeonia decomposita | 122355 | 0.963 |
5 | Moutan rockii_NC037772.1 | Paeonia rockii | 122242 | 0.962 |
6 | Moutan jishanensis_MT210545.1 | Paeonia jishanensis | 121976 | 0.960 |
7 | Moutan delavayi_MT210546.1 | Paeonia delavayi | 116440 | 0.916 |
8 | Moutan ludlowii_NC035623.1 | Paeonia ludlowii | 115813 | 0.911 |
9 | Paeonia anomala_MT210549.1 | Paeonia anomala | 110249 | 0.867 |
10 | Paeonia lactiflora_MN868412.1 | Paeonia lactiflora | 110210 | 0.867 |
11 | Paeonia mairei_MZ617462.1 | Paeonia mairei | 110175 | 0.867 |
12 | Paeonia intermedia_MT210547.1 | Paeonia intermedia | 110084 | 0.866 |
13 | Paeonia veitchii_NC032401.1 | Paeonia veitchii | 109600 | 0.862 |
14 | Paeonia emodi_MT210548.1 | Paeonia emodi | 109542 | 0.862 |
15 | Paeonia obovata_NC026076.1 | Paeonia obovata | 109465 | 0.861 |
16 | Lobidiscus brownii_JQ952560.1 | Paeonia brownii | 104203 | 0.820 |
17 | Cercidiphyllum japonicum_NC037940.1 | Cercidiphyllum japonicum | 44192 | 0.348 |
Table 2. PHS of CPCG between Paeonia lactiflora and some representative species of Paeoniaceae.
No. | Scientific Names and Numbers of CPCG in NCBI | Current Names | PHL/17bp | PHS |
1 | Paeonia lactiflora_MN868412.1 | Paeonia lactiflora | 126772 | 1 |
2 | Paeonia mairei_MZ617462.1 | Paeonia mairei | 126698 | 0.999 |
3 | Paeonia anomala_MT210549.1 | Paeonia anomala | 123509 | 0.974 |
4 | Paeonia veitchii_NC032401.1 | Paeonia veitchii | 121653 | 0.960 |
5 | Paeonia intermedia_MT210547.1 | Paeonia intermedia | 121049 | 0.955 |
6 | Paeonia obovata_NC026076.1 | Paeonia obovata | 120315 | 0.949 |
7 | Paeonia emodi_MT210548.1 | Paeonia emodi | 115807 | 0.914 |
8 | Moutan delavayi_MT210546.1 | Paeonia delavayi | 111923 | 0.883 |
9 | Moutan ludlowii_NC035623.1 | Paeonia ludlowii | 111508 | 0.880 |
10 | Moutan decompositus_NC039425.1 | Paeonia decomposita | 111051 | 0.876 |
11 | Moutan ostii_MK701990.1 | Paeonia ostii | 110968 | 0.875 |
12 | Moutan jishanensis_MT210545.1 | Paeonia jishanensis | 110693 | 0.873 |
13 | Moutan qiui_MT210544.1 | Paeonia qiui | 110631 | 0.873 |
14 | Moutan rockii_NC037772.1 | Paeonia rockii | 110547 | 0.872 |
15 | Moutan suffruticosus_JQ952559.1 | Paeonia suffruticosa | 110217 | 0.869 |
16 | Lobidiscus brownii_JQ952560.1 | Paeonia brownii | 103350 | 0.815 |
17 | Cercidiphyllum japonicum_NC037940.1 | Cercidiphyllum japonicum | 44551 | 0.351 |
Table 3. PHS of CPCG between Lobidiscus brownii and some representative species of Paeoniaceae.
No. | Scientific Names and Numbers of CPCG in NCBI | Current Names | PHL/17bp | PHS |
1 | Lobidiscus brownii_JQ952560.1 | Paeonia brownii | 126326 | 1 |
2 | Moutan delavayi_MT210546.1 | Paeonia delavayi | 105782 | 0.837 |
3 | Moutan ludlowii_NC035623.1 | Paeonia ludlowii | 105265 | 0.833 |
4 | Moutan ostii_MK701990.1 | Paeonia ostii | 105032 | 0.831 |
5 | Moutan decompositus_NC039425.1 | Paeonia decomposita | 104898 | 0.830 |
6 | Moutan jishanensis_MT210545.1 | Paeonia jishanensis | 104580 | 0.828 |
7 | Moutan qiui_MT210544.1 | Paeonia qiui | 104507 | 0.827 |
8 | Moutan rockii_NC037772.1 | Paeonia rockii | 104388 | 0.826 |
9 | Moutan suffruticosus_JQ952559.1 | Paeonia suffruticosa | 104209 | 0.825 |
10 | Paeonia anomala_MT210549.1 | Paeonia anomala | 103392 | 0.819 |
11 | Paeonia lactiflora_MN868412.1 | Paeonia lactiflora | 103353 | 0.818 |
12 | Paeonia mairei_MZ617462.1 | Paeonia mairei | 103345 | 0.818 |
13 | Paeonia intermedia_MT210547.1 | Paeonia intermedia | 103179 | 0.817 |
14 | Paeonia emodi_MT210548.1 | Paeonia emodi | 102903 | 0.815 |
15 | Paeonia obovata_NC026076.1 | Paeonia obovata | 102722 | 0.813 |
16 | Paeonia veitchii_NC032401.1 | Paeonia veitchii | 102721 | 0.813 |
17 | Cercidiphyllum japonicum_NC037940.1 | Cercidiphyllum japonicum | 43220 | 0.342 |
Table 4. PHS of CPCG between Cercidiphyllum japonicum and some representative species of Paeoniaceae.
No. | Scientific Names and Numbers of CPCG in NCBI | Current Names | PHL/17bp | PHS |
1 | Cercidiphyllum japonicum_NC037940.1 | Cercidiphyllum japonicum | 133181 | 1 |
2 | Moutan delavayi_MT210546.1 | Paeonia delavayi | 44789 | 0.336 |
3 | Moutan decompositus_NC039425.1 | Paeonia decomposita | 44777 | 0.336 |
4 | Moutan jishanensis_MT210545.1 | Paeonia jishanensis | 44754 | 0.336 |
5 | Moutan qiui_MT210544.1 | Paeonia qiui | 44731 | 0.336 |
6 | Moutan ostii_MK701990.1 | Paeonia ostii | 44719 | 0.336 |
7 | Moutan rockii_NC037772.1 | Paeonia rockii | 44677 | 0.336 |
8 | Moutan ludlowii_NC035623.1 | Paeonia ludlowii | 44627 | 0.335 |
9 | Paeonia lactiflora_MN868412.1 | Paeonia lactiflora | 44554 | 0.335 |
10 | Paeonia anomala_MT210549.1 | Paeonia anomala | 44539 | 0.334 |
11 | Paeonia mairei_MZ617462.1 | Paeonia mairei | 44536 | 0.334 |
12 | Paeonia emodi_MT210548.1 | Paeonia emodi | 44467 | 0.334 |
13 | Paeonia obovata_NC026076.1 | Paeonia obovata | 44415 | 0.334 |
14 | Paeonia intermedia_MT210547.1 | Paeonia intermedia | 44381 | 0.333 |
15 | Paeonia veitchii_NC032401.1 | Paeonia veitchii | 44340 | 0.333 |
16 | Moutan suffruticosus_JQ952559.1 | Paeonia suffruticosa | 44197 | 0.332 |
17 | Lobidiscus brownii_JQ952560.1 | Paeonia brownii | 43221 | 0.325 |
From
Table 1 to
Table 3, it can be concluded that using the types of
Moutan suffruticosus (Andrews) D. L. Fu,
Paeonia lactiflora Pall. and
Lobidiscus brownii (Hook.) D. L. Fu respectively, Paeoniaceae (Bercht. & J. Presl) Rudolphi obviously include 3 genera:
Moutan Rchb.,
Paeonia L., and
Lobidiscus D. L. Fu, which all have the same evolutionary boundary: PHS (17bp) ≥ 0.90 (intrageneric) or PHS (17bp) ≤ 0.89 (intergeneric). Therefore, the 3 genera system of Paeoniaceae is natural by the chloroplast complete genomic evolutionomy.
From
Table 4, it is evident that the PHL between
Cercidiphyllum japonicum Siebold & Zucc. and
Moutan delavayi (Franch.) D. L. Fu is 44789 more than other species. It means the genus
Moutan Rchb. is the most primitive genus of Paeoniaceae.
Based on
Table 1 to
Table 4, the evolutionary system of genera of Paeoniaceae is presented as
Figure 1. The figure provides a clearly evolutionary context within the family Paeoniaceae (Bercht. & J. Presl) Rudolphi, indicating that the newly established genus
Lobidiscus D. L. Fu is derived from the most primitive genus
Moutan Rchb., rather than from
Paeonia L.. This conclusion is supported by the maximum PHS value of 0.837 between
Lobidiscus brownii (Hook.) D. L. Fu and
Moutan delavayi (Franch.) D. L. Fu (
Table 3), as determined through CPCG evolutionary analyses.
Figure 1. Evolutionary system of genera of Paeoniaceae.
3.2. Synonyms of Liquidambar Genus
Using the type of
Liquidambar formosana Hance, the PHS of CPCG of 6 species of Liquidambaraceae D. L. Fu are analyzed, and the results are presented in
Table 5.
Table 5. PHS of CPCG between Liquidambar formosana and some representative species of Liquidambaraceae.
No. | Scientific Names and Numbers of CPCG in NCBI | Current Names | PHL/17bp | PHS |
1 | Liquidambar formosana_KC588388.1 | Liquidambar formosana | 133703 | 1 |
2 | Liquidambar chinensis_NC047288.1 | Altingia chinensis | 133531 | 0.999 |
3 | Liquidambar cathayensis_MN410884.1 | Semiliquidambar cathayensis | 132359 | 0.990 |
4 | Cercidiphyllum japonicum_NC037940.1 | Cercidiphyllum japonicum | 83212 | 0.622 |
5 | Exbucklandia populnea_NC065400.1 | Exbucklandia populnea | 78802 | 0.589 |
6 | Hamamelis mollis_NC037881.1 | Hamamelis mollis | 77977 | 0.583 |
From
Table 5, it is evident that using the type of
Liquidambar formosana Hance, the genera of
Altingia Noronha and
Semiliquidambar H. T. Chang are the synonyms of the genus
Liquidambar L., owing to their evolutionary relationships with the type far from reaching the minimum criterion PHS (17bp) ≤ 0.928 (intergeneric) for genus classification. Therefore, it can be confirmed that the combination of the genus
Liquidambar L. by Ickert-Bond & Wen
[24] | Ickert-Bond, S. M., Pigg, K. B., Wen, J. Comparative Infructescence Morphology in Altingia (Altingiaceae) and Discordance between Morphological and Molecular Phylogenies. Amer. J. Bot. 2007, 94(7), 1094–1115. https://doi.org/10.3732/ajb.94.7.1094 |
[24]
is scientific. However, the nine specific combinations of the genus are not validly published according to the relevant articles of International Code of Botanical Nomenclature.
3.3. Synonyms of Hamamelis Genus
Using the type of
Hamamelis mollis Oliv., the PHS of CPCG of 7 species of Hamamelidaceae R. Br. are analyzed, and the results are presented in
Table 6.
Table 6. PHS of CPCG between Hamamelis mollis and some representative species of Hamamelidaceae.
No. | Scientific Names and Numbers of CPCG in NCBI | Current Names | PHL/17bp | PHS |
1 | Hamamelis mollis_NC037881.1 | Hamamelis mollis | 133081 | 1 |
2 | Hamamelis sinensis_MT323104.1 | Sycopsis sinensis | 124249 | 0.934 |
3 | Hamamelis racemosum_MZ571522.1 | Distylium racemosum | 124146 | 0.933 |
4 | Hamamelis subaequalis_NC037243.1 | Parrotia subaequalis | 123821 | 0.930 |
5 | Eustigma oblongifolium_NC071207.1 | Eustigma oblongifolium | 114012 | 0.857 |
6 | Sinowilsonia henryi_NC036069.1 | Sinowilsonia henryi | 112888 | 0.848 |
7 | Fortunearia sinensis_NC041487.1 | Fortunearia sinensis | 112522 | 0.846 |
Table 6 indicates that using the type of
Hamamelis mollis Oliv., the genera of
Sycopsis Oliv.,
Distylium Sieb. & Zucc., and
Parrotia C. A. Mey. are the synonyms of the genus
Hamamelis L., because of their evolutionary relationships with the type not meeting the minimum criterion PHS (17bp) ≤ 0.928 (intergeneric) for genus classification. Therefore, it is scientific to combine
Hamamelis L. genus as follows.
Hamamelis L., Sp. Pl. 1: 124 (1753). Type: Hamamelis virginiana L. ─ Distylium Sieb. & Zucc., Fl. Jap. (Sieb.) 1: 178, t. 94. 1841. Type: Hamamelis racemosa (Sieb. & Zucc.) D. L. Fu. ─ Parrotia C. A. Mey., Verz. Pfl. Casp. Meer. 46. 1831. Type: Hamamelis persica DC. ─ Sycopsis Oliv., Trans. Linn. Soc. London 23(1): 83, t. 8. 1860. Type: Hamamelis sinensis (Oliv). D. L. Fu.
About 25 species, in Asia and America, including 18 new specific combinations.
4. New Genus Lobidiscus D. L. Fu
Lobidiscus D. L. Fu, gen. nov. Moutan Rchb. et Paeonia L. similis, sed herbis perennus, cespitosis et semi-decumbentus, foliolis profunde dissectis, discis carnosis, lobatis cum nectarifluis, basis carpellis circumdatis.
Perennial herbs, cespitose and semi-decumbent. Roots fleshy and large. Multi-stems semi-decumbent. Leaves 5-7, alternate, biternate; leaflets deeply dissected. Flowers large, nodding, solitary and termina on a stem, more than 4 cm in diam. Sepals 5–6, purplish green, ovate to sub-orbicular, overlapping, and cupped. Petals 5–10, orbicular, varying in color from crimson, brownish maroon to yellow on the margins. Stamens numerous, yellow. Disc fleshy, with about 12 nectariferous lobes, encircled the bases of carpels. Carpels 3-6, free; ovules numerous, borne in two rows along ventral suture. Styles short; stigmas laterally flattened, recurved. Fruit a follicle. Seeds yellowish tan to black, globose, or ovoid-globose, 6-11 mm in diam. diploid (2N = 10).
Type: Lobidiscus californicus (Nutt.) D. L. Fu.
2 species, in America. Lobidiscus californicus (Nutt.) D. L. Fu and Lobidiscus brownii (Hook.) D. L. Fu.
5. New Names of Some Families
The family name, Altingiaceae Lindl. (1846) nom. cons., fails to comply with the fundamental principles of the International Code of Botanical Nomenclature due to the inappropriate type, namely Altingia Noronha, being a synonym of Liquidambar L.. Replacing the family name with a scientific and standardized one will be an inevitable tendency in the advancement of plant taxonomy. This circumstance is not an isolated instance. Some conserved family names that employ synonyms or illegal types have been compiled, and their scientific names have been determined as follows.
Aesculaceae D. L. Fu, fam. nom. nov. Hippocastanaceae A. Rich., Bot. Méd.: 680. Jun 1823, nom. cons. Typus: Aesculus L. (Hippocastanum Mill., nom. syn.).
Amphipterygiaceae D. L. Fu, fam. nom. nov. Julianiaceae Hemsl. in J. Bot. 44: 379. Oct 1906, nom. cons. Typus: Amphipterygium Standl. (Juliania Schltdl., nom. illeg.)
Dianthaceae D. L. Fu, fam. nom. nov. Caryophyllaceae Juss., Gen. Pl.: 299. 4 Aug 1789, nom. cons. Typus: Dianthus L. (Caryophyllus Mill., nom. illeg.).
Diospyraceae D. L. Fu, fam. nom. nov. Ebenaceae Gürke in Engler & Prantl, Nat. Pflanzenfam. 4(1): 153. Dec 1891, nom. cons. Typus: Diospyros L. (Ebenus Kuntze, nom. illeg.).
Drimydaceae D. L. Fu, fam. nom. nov. Winteraceae R. Br. ex Lindl., Intr. Nat. Syst. Bot.: 26. Sep 1830, nom. cons. Typus: Drimys J. R. Forst. & G. Forst., nom. cons. (Wintera Murray, nom. illeg.).
Ilecaceae D. L. Fu, fam. nom. nov. Aquifoliaceae DC. ex A. Rich., Nouv. Elém. Bot., ed. 4: 555. 1828, nom. cons. Typus: Ilex L. (Aquifolium Mill., nom. illeg.).
Liquidambaraceae D. L. Fu, fam. nom. nov. Altingiaceae Lindl., Veg. Kingd.: 253. Jan-Mai 1846, nom. cons. Typus: Liquidambar L. (Altingia Noronha, nom. syn.)
Loniceraceae D. L. Fu, fam. nom. nov. Caprifoliaceae Adans., Fam. Pl. 2: 153. Jul-Aug 1763, nom. cons. Typus: Lonicera L. (Caprifolium Mill., nom. syn.).
Mammillariaceae D. L. Fu, fam. nom. nov. Cactaceae Juss., Gen. Pl.: 310. 4 Aug 1789, nom. cons. Typus: Mammillaria Haw., nom. cons. (Cactus L., nom. rej.).
Mirabilidaceae D. L. Fu, fam. nom. nov. Nyctaginaceae Juss., Gen. Pl.: 90. 4 Aug 1789, nom. cons. Typus: Mirabilis L. (Nyctago Juss., nom. syn.).
Oenotheraceae D. L. Fu, fam. nom. nov. Onagraceae Adans., Fam. Pl. 2: 81. Jul-Aug 1763, nom. cons. Typus: Oenothera L. (Onagra Mill., nom. syn.).
Triglochinaceae D. L. Fu, fam. nom. nov. Juncaginaceae Rich., Démonstr. Bot.: ix. Mai 1808, nom. cons. Typus: Triglochin L. (Juncago Ség., nom. syn.).
Utriculariaceae D. L. Fu, fam. nom. nov. Lentibulariaceae Rich., Fl. Paris. (Poiteau & Turpin) 1: 23 (ed. fol.), 26 (ed. qto.) 1808, nom. cons. Typus: Utricularia L. (Lentibularia Ség., nom. syn.).
6. New Specific Combinations
Hamamelis annamica (Gagnep.) D. L. Fu, sp. transl. nov. Saxifragites annamicus Gagnep., Notul. Syst. (Paris) 14: 34. 1950.
Hamamelis buxifolia (Hance) D. L. Fu, sp. transl. nov. Myrsine buxifolia Hance, Ann. Sci. Nat., Bot., sér. 4, 15: 225. 1861.
Hamamelis hubeiensis D. L. Fu, sp. nom. nov. Distylium racemosum var. chinense Franch. ex Hemsl., J. Linn. Soc., Bot. 23: 290. 1887, non Hamamelis chinensis R. Br.; Distylium chinense (Franch. ex Hemsl.) Diels, Bot. Jahrb. Syst. 29: 290. 1900.
Hamamelis chungii (F. P. Metcalf) D. L. Fu, sp. transl. nov. Sycopsis chungii F. P. Metcalf, Lingnan Sci. J. 10: 414. 1931.
Hamamelis cuspidata (H. T. Chang) D. L. Fu, sp. transl. nov. Distylium cuspidatum H. T. Chang, Acta Sci. Nat. Univ. Sunyatseni (2): 38. 1959.
Hamamelis dunniana (H. Lév.) D. L. Fu, sp. transl. nov. Distylium dunnianum H. Lév., Repert. Spec. Nov. Regni Veg. 11: 67. 1912.
Hamamelis elaeagnoides (H. T. Chang) D. L. Fu, sp. transl. nov. Distylium elaeagnoides H. T. Chang, Acta Sci. Nat. Univ. Sunyatseni (2): 37. 1959.
Hamamelis gracilis (Nakai) D. L. Fu, sp. transl. nov. Distylium gracile Nakai, J. Arnold Arbor. 5: 77. 1924.
Hamamelis indica (C. B. Clarke) D. L. Fu, sp. transl. nov. Distylium indicum Benth. ex C. B. Clarke, Fl. Brit. India [J. D. Hooker] 2(5): 427. 1878.
Hamamelis lepidota (Nakai) D. L. Fu, sp. transl. nov. Distylium lepidotum Nakai, Bot. Mag. (Tokyo) 32: 220. 1918.
Hamamelis grandifolia D. L. Fu, sp. nom. nov. Distylium macrophyllum H. T. Chang, Acta Sci. Nat. Univ. Sunyatseni (1): 39. 1960, non Hamamelis macrophylla Pursh.
Hamamelis myricoides (Hemsl.) D. L. Fu, sp. transl. nov. Distylium myricoides Hemsl. in Hooker's Icon. Pl. 29: sub t. 2835. 1907.
Hamamelis pingpienensis (Hu) D. L. Fu, sp. transl. nov. Sycopsis pingpienensis Hu, Bull. Fan Mem. Inst. Biol., Bot. 10: 149. 1940.
Hamamelis racemosa (Sieb. & Zucc.) D. L. Fu, sp. transl. nov. Distylium racemosum Sieb. & Zucc., Fl. Jap. 1: 179. 1841.
Hamamelis sinensis (Oliv.) D. L. Fu, sp. transl. nov. Sycopsis sinensis Oliv. in Hooker's Icon. Pl. 20: t. 1931. 1890.
Hamamelis stellaris (Kuntze) D. L. Fu, sp. transl. nov. Distylium stellare Kuntze, Revis. Gen. Pl. 1: 233. 1891.
Hamamelis triplinervia (H. T. Chang) D. L. Fu, sp. transl. nov. Sycopsis triplinervia H. T. Chang, Acta Sci. Nat. Univ. Sunyatseni (1): 41. 1960.
Hamamelis tsiangii (Cheng) D. L. Fu, sp. transl. nov. Distylium tsiangii Chun ex Cheng, Contr. Biol. Lab. Sci. Soc. China, Bot. Ser. viii. 142. 1932; et in J. Arnold Arbor. 25: 330. 1944.
Liquidambar cambodiana (Lecomte) D. L. Fu, sp. transl. nov. Altingia cambodiana Lecomte, Bull. Mus. Hist. Nat. Paris 30: 391. 1924.
Liquidambar caudata (H. T. Chang) D. L. Fu, sp. transl. nov. Semiliquidambar caudata H. T. Chang, Acta Sci. Nat. Univ. Sunyatseni, 39. 1962.
Liquidambar chingii (Metcalf) D. L. Fu, sp. transl. nov. Altingia chingii Metcalf, Lingnan Sc. Journ. 10: 413. 1931.
Liquidambar gracilipes (Hemsl.) D. L. Fu, sp. transl. nov. Altingia gracilipes Hemsl., in Hook. Ic. Pl. t. 2837. 1907.
Liquidambar multinervis (Cheng) D. L. Fu, sp. transl. nov. Altingia multinervis Cheng, in Notes For. Inst. Nat. Centr. Univ. Nanking, Dendrol. Ser., No. 1, 3. 1947.
Liquidambar obovata (Merrill & Chun) D. L. Fu, sp. transl. nov. Altingia obovata Merrill & Chun, in Sunyatsenia, 2: 238. 1935.
Liquidambar poilanei (Tardieu) D. L. Fu, sp. transl. nov. Altingia poilanei Tardieu, Fl. Camb., Laos & Vietn., Fasc. 4. 95. 1965.
Liquidambar siamensis (Craib) D. L. Fu, sp. transl. nov. Altingia siamensis Craib, Kew Bull. 68. 1928.
Liquidambar yunnanensis (Rehd. & Wils.) D. L. Fu, sp. transl. nov. Altingia yunnanensis Rehd. & Wils. in Sargent Pl. Wilson. I: 422. 1913.
Lobidiscus brownii (Hook.) D. L. Fu, sp. transl. nov. Paeonia brownii Douglas ex Hook., Fl. Bor.-Amer. (Hooker) 1(1): 27. 1829.
Lobidiscus californicus (Nutt.) D. L. Fu, sp. transl. nov. Paeonia californica Nutt., Fl. N. Amer. (Torr. & A. Gray) 1(1): 41. 1838.
Moutan baokangensis (Z. L. Dai & T. Hong) D. L. Fu, sp. transl. nov. Paeonia baokangensis Z. L. Dai & T. Hong, Bull. Bot. Res., Harbin 17(1): 2. 1997.
Moutan decompositus (Hand.-Mazz.) D. L. Fu, sp. transl. nov. Paeonia decomposita Hand.-Mazz., Acta Horti Gothob. 13: 39. 1939.
Moutan delavayi (Franch.) D. L. Fu, sp. transl. nov. Paeonia delavayi Franch., Bull. Soc. Bot. France 33: 382. 1887.
Moutan jishanensis (T. Hong & W. Z. Zhao) D. L. Fu, sp. transl. nov. Paeonia jishanensis T. Hong & W. Z. Zhao, Bull. Bot. Res., Harbin 12(3): 225. 1992.
Moutan ludlowii (Stern & G. Taylor) D. L. Fu, sp. comb. nov. Paeonia lutea var. ludlowii Stern & G. Taylor, J. Roy. Hort. Soc. 6: 217. 1851; Paeonia ludlowii (Stern & G. Taylor) D. Y. Hong, Novon 7(2): 157. 1997.
Moutan ostii (T. Hong & J. X. Zhang) D. L. Fu, sp. transl. nov. Paeonia ostii T. Hong & J. X. Zhang, Bull. Bot. Res., Harbin 12(3): 223. 1992.
Moutan potaninii (Komarov) D. L. Fu, sp. transl. nov. Paeonia potaninii Komarov, Bot. Mater. Gerb. Glavn. Bot. Sada R. S. F. S. R. 2: 7. 1921.
Moutan qiui (Y. L. Pei & D. Y. Hong) D. L. Fu, sp. transl. nov. Paeonia qiui Y. L. Pei & D. Y. Hong, Acta Phytotax. Sin. 33(1): 91. 1995.
Moutan rockii (S. G. Haw & Lauener) D. L. Fu, sp. comb. nov. Paeonia suffruticosa subsp. rockii S. G. Haw & Lauener, Edinburgh J. Bot. 47(3): 279. 1990; Paeonia rockii (S. G. Haw & Lauener) T. Hong & J. J. Li ex D. Y. Hong, Acta Phytotax. Sin. 36(6): 539. 1998.
Moutan rotundilobus (D. Y. Hong) D. L. Fu, sp. comb. nov. Paeonia decomposita subsp. rotundiloba D. Y. Hong, Kew Bull. 52(4): 961. 1997; Paeonia rotundiloba (D. Y. Hong) D. Y. Hong, J. Syst. Evol. 49(5): 465. 2011.
Moutan suffruticosus (Andrews) D. L. Fu, sp. transl. nov. Paeonia suffruticosa Andrews, Bot. Repos. 6: t. 373. 1804.
Moutan yananensis (T. Hong & M. R. Li) D. L. Fu, sp. transl. nov. Paeonia yananensis T. Hong & M. R. Li, Bull. Bot. Res., Harbin 12(3): 226. 1992.
7. Conclusion
The evolutionary system of the genera within Paeoniaceae (Bercht. & J. Presl) Rudolphi has been initially established, encompassing three natural genera: Moutan Rchb., Paeonia L., and Lobidiscus D. L. Fu, all sharing a common evolutionary boundary defined by PHS (17bp) ≥ 0.90 (intrageneric) or PHS (17bp) ≤ 0.89 (intergeneric). The most primitive genus in this family is Moutan Rchb. Notably, the new genus Lobidiscus D. L. Fu, gen. nov., characterized by its distinctly lobed floral discs, is described herein with Lobidiscus californicus (Nutt.) D. L. Fu designated as the type species; this new genus originates from Moutan Rchb. (1827), rather than Paeonia L., as evidenced by a maximum PHS value of 0.837 between Lobidiscus brownii (Hook.) D. L. Fu and Moutan delavayi (Franch.) D. L. Fu based on CPCG evolutionary analyses. Two synonyms of the genus Liquidambar L. (1753), Altingia Noronha and Semiliquidambar H. T. Chang, have been confirmed, while three current synonyms of the genus Hamamelis L. (1753), including Distylium Siebold & Zucc., Parrotia C. A. Mey. and Sycopsis Oliv., have also been scientifically identified. Additionally, 13 novel family names, two new specific epithets, and 39 newly valid specific combinations have been published in accordance with the scientific criterion. These contributions will provide a robust foundation for future research into the evolutionary systems within the order Hamamelidales Griseb. and serve an indicative function in subsequent investigations regarding the scientific definition of genus and scientifically resolving confusions of certain genera within the phylum Fructophyta D. L. Fu & H. Fu.
Abbreviations
CPCG | Chloroplast Complete Genomes |
PHL | Phylogenetic Loci |
PHS | Phylogenetic Similarity |
Author Contributions
Da-Li Fu is the sole author. The author read and approved the final manuscript.
Conflicts of Interest
The author declares no conflicts of interest.
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Cite This Article
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@article{10.11648/j.ajaf.20241205.14,
author = {Da-Li Fu},
title = {New Genus Lobidiscus and New Combinations of Genera of Moutan, Liquidambar and Hamamelis (Hamamelidales)
},
journal = {American Journal of Agriculture and Forestry},
volume = {12},
number = {5},
pages = {346-355},
doi = {10.11648/j.ajaf.20241205.14},
url = {https://doi.org/10.11648/j.ajaf.20241205.14},
eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajaf.20241205.14},
abstract = {Hamamelidales Griseb. (1854) order serves as a foundational group and plays a significant role in the research of evolutionary systematics of the class Rosopsida Batsch (1802) of Fructophyta D. L. Fu & H. Fu (2018). To address the ambiguities surrounding the circumscription of certain genera within this order, such as Paeonia L. (1753), Liquidambar L. (1753), and Hamamelis L. (1753), relevant chloroplast complete genome sequences from the NCBI database were retrieved, and evolutionary analyses were conducted on these sequences in this study. Notably, Lobidiscus D. L. Fu, gen. nov., a new genus endemic to America characterized by its distinctly lobed floral discs, has been separated from Paeonia L. belonging to Paeoniaceae (Bercht. & J. Presl) Rudolphi, nom. cons. (1830), and Lobidiscus californicus (Nutt.) D. L. Fu is designated as its type species. This new genus derives from Moutan Rchb. (1827), rather than Paeonia L., given that a maximum PHS value of 0.837 were observed between Lobidiscus brownii (Hook.) D. L. Fu and Moutan delavayi (Franch.) D. L. Fu based on CPCG evolutionary analyses. Meanwhile, the application of the minimum criterion PHS ≤ 0.928 (intergeneric, CPCG) for genus classification of Fructophyta D. L. Fu & H. Fu, has led to confirmation of two synonyms for Liquidambar L.: Altingia Noronha and Semiliquidambar H. T. Chang; additionally, three current synonyms for Hamamelis L., including Distylium Siebold & Zucc., Parrotia C. A. Mey., and Sycopsis Oliv., have been scientifically identified. In total, 13 novel family names like Liquidambaraceae D. L. Fu, Dianthaceae D. L. Fu, Diospyraceae D. L. Fu and Ilecaceae D. L. Fu have been established, along with two new specific epithets, Hamamelis hubeiensis D. L. Fu and Hamamelis grandifolia D. L. Fu, and 39 newly valid combinations involving Hamamelis L., Liquidambar L., Lobidiscus D. L. Fu, and Moutan Rchb. also been published, such as Hamamelis annamica (Gagnep.) D. L. Fu, Liquidambar cambodiana (Lecomte) D. L. Fu, Lobidiscus brownii (Hook.) D. L. Fu, and Moutan suffruticosus (Andrews) D. L. Fu. These contributions will effectively clarify taxonomic nomenclature confusions in a scientific manner while establishing a robust foundation for further research into the evolutionary systems within the order Hamamelidales Griseb.
},
year = {2024}
}
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TY - JOUR
T1 - New Genus Lobidiscus and New Combinations of Genera of Moutan, Liquidambar and Hamamelis (Hamamelidales)
AU - Da-Li Fu
Y1 - 2024/10/10
PY - 2024
N1 - https://doi.org/10.11648/j.ajaf.20241205.14
DO - 10.11648/j.ajaf.20241205.14
T2 - American Journal of Agriculture and Forestry
JF - American Journal of Agriculture and Forestry
JO - American Journal of Agriculture and Forestry
SP - 346
EP - 355
PB - Science Publishing Group
SN - 2330-8591
UR - https://doi.org/10.11648/j.ajaf.20241205.14
AB - Hamamelidales Griseb. (1854) order serves as a foundational group and plays a significant role in the research of evolutionary systematics of the class Rosopsida Batsch (1802) of Fructophyta D. L. Fu & H. Fu (2018). To address the ambiguities surrounding the circumscription of certain genera within this order, such as Paeonia L. (1753), Liquidambar L. (1753), and Hamamelis L. (1753), relevant chloroplast complete genome sequences from the NCBI database were retrieved, and evolutionary analyses were conducted on these sequences in this study. Notably, Lobidiscus D. L. Fu, gen. nov., a new genus endemic to America characterized by its distinctly lobed floral discs, has been separated from Paeonia L. belonging to Paeoniaceae (Bercht. & J. Presl) Rudolphi, nom. cons. (1830), and Lobidiscus californicus (Nutt.) D. L. Fu is designated as its type species. This new genus derives from Moutan Rchb. (1827), rather than Paeonia L., given that a maximum PHS value of 0.837 were observed between Lobidiscus brownii (Hook.) D. L. Fu and Moutan delavayi (Franch.) D. L. Fu based on CPCG evolutionary analyses. Meanwhile, the application of the minimum criterion PHS ≤ 0.928 (intergeneric, CPCG) for genus classification of Fructophyta D. L. Fu & H. Fu, has led to confirmation of two synonyms for Liquidambar L.: Altingia Noronha and Semiliquidambar H. T. Chang; additionally, three current synonyms for Hamamelis L., including Distylium Siebold & Zucc., Parrotia C. A. Mey., and Sycopsis Oliv., have been scientifically identified. In total, 13 novel family names like Liquidambaraceae D. L. Fu, Dianthaceae D. L. Fu, Diospyraceae D. L. Fu and Ilecaceae D. L. Fu have been established, along with two new specific epithets, Hamamelis hubeiensis D. L. Fu and Hamamelis grandifolia D. L. Fu, and 39 newly valid combinations involving Hamamelis L., Liquidambar L., Lobidiscus D. L. Fu, and Moutan Rchb. also been published, such as Hamamelis annamica (Gagnep.) D. L. Fu, Liquidambar cambodiana (Lecomte) D. L. Fu, Lobidiscus brownii (Hook.) D. L. Fu, and Moutan suffruticosus (Andrews) D. L. Fu. These contributions will effectively clarify taxonomic nomenclature confusions in a scientific manner while establishing a robust foundation for further research into the evolutionary systems within the order Hamamelidales Griseb.
VL - 12
IS - 5
ER -
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