ABSTRACT
The Epipactis helleborine (L.) Crantz group is one of the most taxonomically challenging species complexes within the genus Epipactis. Because of the exceptionally high levels of morphological variability and the ability to readily cross with other species, ninety different taxa at various taxonomic ranks have already been described within its nominative subspecies, but the taxonomic status of most of them is uncertain, widely disputed, and sometimes even irrelevant. The present review is based on results of the most recent research devoted to the E. helleborine group taxonomy. In addition, we analysed data about taxa belonging to this group presented in some research articles and monographs devoted directly to the genus Epipactis or to orchids in certain area(s). Based on the reviewed literature and data collected in four taxonomic databases available online, we propose an updated list of the 10 currently accepted taxa in the E. helleborine group (two species, six subspecies, and two varieties), which includes E. helleborine (L.) Crantz subsp. helleborine; E. helleborine subsp. bithynica (Robatsch) Kreutz; E. helleborine subsp. distans (Arv.-Touv.) R.Engel and P.Quentin; E. helleborine subsp. neerlandica (Verm.) Buttler; E. helleborine var. tangutica (Schltr.) S.C.Chen and G.H.Zhu; E. helleborine subsp. tremolsii (Pau) E.Klein; E. helleborine subsp. voethii (Robatsch) Jakubska-Busse, Zolubak, and Lobas, stat. nov.; E. condensata Boiss. ex D.P.Young; E. condensata var. kuenkeleana (Akhalk., H.Baumann, R.Lorenz, and Mosul.) Popovich; and E. cupaniana C.Brullo, D'Emerico, and Pulv.
ABSTRACT
Epipactis greuteri is an obligate autogamous orchid species. Due to large differences in the interpretation of the diagnosis of this species, it is often mistakenly identified by botanists, which results in erroneous information provided in the literature about its distribution in Europe. In the present paper we review its description, including flower details, gynostemium features, and papillae morphology and compare it to E. helleborine, with which it is often confused. Based on thorough study of herbarium material (including holotype and isotype) and field research in Greece, Romania, and Poland, we confirm that gynostemium of E. greuteri has strongly reduced clinandrium and does not produce viscidium. We also discuss taxonomic treatment of E. preinensis and E. flaminia, two recently described taxa related to E. greuteri. The results of genetic analyses, as well as the range of phenotypic variability of E. greuteri individuals from various regions of Europe were presented and discussed. The analysis based on the ITS (internal transcribed spacer) nuclear marker showed no differences among E. helleborine, E. purpurata, E. albensis, and E. greuteri, which probably indicates their close relationship. Based on the analysis of plastid regions, six haplotypes were detected in all investigated samples. An exhaustive description of morphological features of E. greuteri is provided.
ABSTRACT
The selection and validation of proper distinguishing characters are of crucial importance in taxonomic revisions. The modern classifications of orchids utilize the molecular tools, but still the selection and identification of the material used in these studies is for the most part related to general species morphology. One of the vegetative characters quoted in orchid manuals is leaf arrangement. However, phyllotactic diversity and ontogenetic changeability have not been analysed in detail in reference to particular taxonomic groups. Therefore, we evaluated the usefulness of leaf arrangements in the taxonomy of the genus Epipactis Zinn, 1757. Typical leaf arrangements in shoots of this genus are described as distichous or spiral. However, in the course of field research and screening of herbarium materials, we indisputably disproved the presence of distichous phyllotaxis in the species Epipactis purpurata Sm. and confirmed the spiral Fibonacci pattern as the dominant leaf arrangement. In addition, detailed analyses revealed the presence of atypical decussate phyllotaxis in this species, as well as demonstrated the ontogenetic formation of pseudowhorls. These findings confirm ontogenetic variability and plasticity in E. purpurata. Our results are discussed in the context of their significance in delimitations of complex taxa within the genus Epipactis.
