Research Article
Anemonoides × lipsiensis
comb. nov. (Ranunculaceae), new for the Italian flora
Giovanni Astuti‡,
Giancarlo Marconi§,
Paolo Pupillo|,
Lorenzo Peruzzi‡
‡ Università di Pisa, Pisa, Italy
§ Associazione Pangea, Bologna, Italy
| University of Bologna, Bologna, Italy
Corresponding author:
Giovanni Astuti
(
gastuti@biologia.unipi.it
)
Academic editor: Fabrizio Bartolucci
© 2019 Giovanni Astuti, Giancarlo Marconi, Paolo Pupillo, Lorenzo Peruzzi. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Astuti G, Marconi G, Pupillo P, Peruzzi L (2019) Anemonoides × lipsiensis comb. nov. (Ranunculaceae), new for the Italian flora. Italian Botanist 7: 101-105. https://doi.org/10.3897/italianbotanist.7.35004
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Abstract
The hybrid Anemonoides nemorosa × A. ranunculoides is recorded for the first time in Italy at the southern periphery of Bologna (N Italy, Emilia-Romagna). Its status is supported by both morphological features and chromosome number (2n = 31). For this taxon, a new nomenclatural combination is proposed.
Keywords
chromosome number, hybrid, vascular flora
Introduction
Anemonoides nemorosa (L.) Holub is a circumboreal species, quite common in woods and clearings throughout the Alps and peninsular Italy. Anemonoides ranunculoides (L.) Holub occurs in Europe and the Caucasus area, and is widespread in the forests of northern Italy, but increasingly rare to the south (Pignatti 2017; Bartolucci et al. 2018).
Natural hybrids among these species have been described since the first half of the nineteenth century for several areas of Austria, Germany, Denmark, and Sweden (Pritzel 1841; Beck von Mannagetta 1890; Camus 1898; Hegi 1912; Bernström 1946).
Since 2012, morphologically intermediate individuals have been known at the southern periphery of Bologna, N Italy (Fig. 1), where A. nemorosa and A. ranunculoides co-exist. Given that the first species shows typically 2n = 30 and the second 2n = 32 chromosomes (Mlinarec et al. 2012), we expect that putatively F1 hybrid plants should show 2n = 31, as reported by Bernström (1946) for Sweden.
Material and methods
Specimens seen
Italy. Anemonoides × lipsiensis (Beck) Peruzzi & G.Astuti, Bologna, lungo la strada di Roncrio (UTM WGS84: 44.462742N, 11.336363E), margine di bosco, 120 m, 25 March 2017, G. Astuti, G. Marconi, L. Peruzzi, P. Pupillo (PI, n. 019279). Anemonoides nemorosa (L.) Holub, ibidem (PI, n. 019277). Anemonoides ranunculoides (L.) Holub, ibidem (PI, n. 019278).
Morphological observations
Based on Brennenstuhl (2004), we measured the following characters on three dried individuals for each taxon: number of flowers per shoot, flower colour, flower diameter, number of petals, peduncle length.
Chromosome number
Squash preparations were made on root-tips taken from plants native to the Bologna site and grown in the Botanical Garden of Pisa. Root-tips were pretreated with 0.4% colchicine for 3 hours and then fixed in Carnoy fixative solution for 1 hour. After hydrolysis in HCl 1N at 60 °C, the tips were stained in leuco-basic fuchsine.
Results
Results of morphological observations are reported in Table 1. For all the features evaluated, the putative hybrid shows intermediate values between those of putative parental species.
Floral morphological features of Anemonoides nemorosa, A. × lipsiensis, and A. ranunculoides in the investigated site.
|
A. nemorosa
|
A. × lipsiensis
|
A. ranunculoides
|
Number of flowers per shoot |
1 |
1–2 |
2 |
Flower colour |
white |
pale yellow |
yellow |
Flower diameter (cm) |
4.0–4.5 |
3.0–3.5 |
2.0–2.5 |
Number of petals |
7 |
5–7 |
5 |
Peduncle length (cm) |
6.5–8.0 |
4.5–6.0 |
3.0–4.0 |
The putatively hybrid plants show 2n = 31 chromosomes.
Discussion
The morphological features of the plants studied agree perfectly with those reported for the hybrid A. nemorosa ×A. ranunculoides from Saxony-Anhalt, NE Germany, ca. 200 km N-NW to Leipzig (Brennenstuhl 2004). Our chromosome count carried out on the Italian population, 2n = 31, also agrees with previous counts based on extra-Italian material (Bernström 1946).
The circumscription of tribe Anemoninae has been much controversial in recent years, and a wide array of taxonomic solutions were proposed, ranging from the inclusion of a number of morphologically well-established genera in a large and highly heterogeneous Anemone (Hoot et al. 2012), to the disintegration of the traditional concept of Anemone in a number of smaller genera (e.g., Mosyakin 2016; Bartolucci et al. 2018; Christenhusz et al. 2018) to allow the recognition of monophyletic groups. Among the scholars favouring this latter approach, the taxonomic independence of the genus Anemonoides Mill. (= Anemone sect. Anemonanthea DC.) is disputed by some authors preferring a wider concept of Anemone (e.g., Ziman et al. 2008; Mosyakin 2016; Pignatti 2017). On the contrary, other authors as Starodubtsev (1991), Banfi et al. (2005), and Bartolucci et al. (2018) recognize it as a distinct genus, an option we also follow here. Under Anemonoides, the hybrid A. nemorosa × A. ranunculoides has been named A. × seemenii (E.G.Camus) Holub so far (Holub 1983). However, the name holding priority at (notho-)species level is Anemone × lipsiensis Beck, so that the following new combination is needed under that genus:
Anemonoides
×
lipsiensis
(Beck) Peruzzi & G.Astuti, comb. nov.
Anemone × lipsiensis
Beck, Fl. Nieder-Österreich 1: 407. 1890 (Basionym)
= Anemone × vindobonensis Beck, Fl. Nieder-Österreich 1: 407. 1890
= Anemone × seemenii E.G.Camus, J. Bot. (Morot) 12: 101. 1898 ≡ Anemonoides × seemenii (E.G.Camus) Holub, Folia Geobot. Phytotax. 18(2): 206. 1983
– Anemone intermedia M.Winkl. ex Pritz., Linnaea 15: 652. 1842, nom. nud.
Note
Beck von Mannagetta (1890) lists A. lipsiensis and A. vindobonensis as “6a” and “6b” respectively, “6” representing the same hybrid formula “A. nemorosa × ranunculoides” (Beck von Mannagetta 1890: 406). This guarantees that he considered both these taxa as nothospecies (from the Preface at pag. V: “...sämmtliche Kreutzungen zweier Arten wurden unter einer Nummer vereinigt und die einzelnen Hybriden, insoweit deren Unterscheidung überhaupt möglich ist, unter den gemeinsamen Nummer mit fortlaufenden Buchstaben bezeichnet.” [“...all the crosses between two species are united under the same number and the single hybrids, unless they can be differentiated, are indicated by that number followed by consecutive letters”]). Consequently, both names are legitimate (Art. H.4 of ICN, Turland et al. 2018) and of equal priority (Art. 11.5 of ICN), so that we select here A. lipsiesis as priority name.
References
-
Beck von Mannagetta GR (1890) Flora von Nieder-Österreich 1. Carl Gerold’s Sohn, Wien, 430 pp.
-
Banfi E, Galasso G, Soldano A (2005) Notes on systematics and taxonomy for the Italian vascular flora. 1. Atti della Società Italiana di Scienze Naturali, Museo Civico di Storia Naturale di Milano 146(2): 219–244.
-
Bartolucci F, Peruzzi L, Galasso G, Albano A, Alessandrini A, Ardenghi NMG, Astuti G, Bacchetta G, Ballelli S, Banfi E, Barberis G, Bernardo L, Bouvet D, Bovio M, Cecchi L, Di Pietro R, Domina G, Fascetti S, Fenu G, Festi F, Foggi B, Gallo L, Gubellini L, Gottschlich G, Iamonico D, Iberite M, Jinénez-Mejías P, Lattanzi E, Martinetto E, Masin RR, Medagli P, Passalacqua NG, Peccenini S, Pennesi R, Pierini B, Poldini L, Prosser F, Raimondo FM, Marchetti D, Roma-Marzio F, Rosati L, Santangelo A, Scoppola A, Scortegagna S, Selvaggi A, Selvi F, Soldano A, Stinca A, Wagensommer RP, Wilhalm T, Conti F (2018) An updated checklist of the vascular flora native to Italy. Plant Biosystems 152(2): 179–303. https://doi.org/10.1080/11263504.2017.1419996
-
Brennenstuhl G (2004) Anemone × lipsiensis G.Beck im Bürgerholz bei Salzwedel. Mitteilungen zur floristischen Kartierung Sachsen-Anhalts 9: 27–31.
-
Camus MEG (1898) Statistique ou catalogue des plantes hybrides spontanées de la flore européenne. Journal de Botanique 12: 97–103.
-
Christenhusz MJM, Fay MF, Byng JW (Eds) (2018) The Global Flora. Vol. 4: Special Edition, GLOVAP Nomenclature Part 1. Plant Gateway Ltd. , Bradford, United Kingdom, 155 pp.
-
Hegi G (1912) Illustrierte Flora von Mittel-Europa. Band III. A. Pichler’s Witwe & John, Wien, 607 pp.
-
Hoot SB, Meyer KM, Manning JC (2012) Phylogeny and reclassification of Anemone (Ranunculaceae), with an emphasis on Austral species. Systematic Botany 37: 139–152. https://doi.org/10.1600/036364412X616729
-
Mlinarec J, Šatović Z, Mihelj D, Malenica N, Besendorfer W (2012) Cytogenetic and phylogenetic studies of diploid and polyploid members of Tribe Anemoninae (Ranunculaceae). Plant Biology 14: 525–536. https://doi.org/10.1111/j.1438-8677.2011.00519.x
-
Mosyakin SL (2016) Nomenclatural notes on North American taxa of Anemonastrum and Pulsatilla (Ranunculaceae), with comments on the circumscription of Anemone and related genera. Phytoneuron 2016–79: 1–12.
-
Pignatti S (2017) Flora d’Italia. Vol. 1, ed. 2. Edagricole-New Business Media, Milano, 1064 pp.
-
Starodubtsev VN (1991) Anemones: Systematics and Evolution. Nauka, Leningrad. [In Russian]
-
Turland NJ, Wiersema JH, Barrie FR, Greuter W, Hawksworth DL, Herendeen PS, Knapp S, Kusber W-H, Li D-Z, Marhold K, May TW, McNeill J, Monro AM, Prado J, Price MJ, Smith GF (Eds) (2018) International Code of Nomenclature for algae, fungi, and plants (Shenzhen Code) adopted by the Nineteenth International Botanical Congress Shenzhen, China, July 2017. Regnum Vegetabile 159: 1–254. https://doi.org/10.12705/Code.2018
-
Ziman SN, Bulakh EV, Kadota Y, Keener CS (2008) Modern view on the taxonomy of the genus Anemone L. sensu stricto (Ranunculaceae). Journal of Japanese Botany 83: 127–155.