The moss flora of Europe and Macaronesia comprises 278 genera, 1292 species, 46 subspecies and 118 varieties. Of the total 1292 species, 53 are confined to Macaronesia and 21 are thought to be non-native. The checklist was derived from those for the various component countries and regions. It is based on results published up to the end of 2005. Subspecies and varieties are included; hybrids are omitted. The taxonomic hierarchy is based on one published by Goffinet & Buck in 2004. While it has been strongly influenced by results of modern molecular methods, there are still many remaining uncertainties, even at family level. Because of these uncertainties, taxonomic innovation has generally been avoided. There are four new combinations and one change of status.

Introduction. Following on from work on the European bryophyte Red List, the taxonomically and nomenclaturally updated spreadsheets used for that project have been expanded into a new checklist for the bryophytes of Europe. Methods. A steering group of ten European bryologists was convened, and over the course of a year, the spreadsheets were compared with previous European checklists, and all changes noted. Recent literature was searched extensively. A taxonomic system was agreed, and the advice and expertise of many European bryologists sought. Key results. A new European checklist of bryophytes, comprising hornworts, liverworts and mosses, is presented. Fifteen new combinations are proposed. Conclusions. This checklist provides a snapshot of the current European bryophyte flora in 2019. It will already be out-of-date on publication, and further research, particularly molecular work, can be expected to result in many more changes over the next few years.

Earlier phylogenetic studies, including species belonging to the Neckeraceae, have indicated that this pleurocarpous moss family shares a strongly supported sister group relationship with the Lembophyllaceae, but the family delimitation of the former needs adjustment. To test the monophyly of the Neckeraceae, as well as to redefine the family circumscription and to pinpoint its phylogenetic position in a larger context, a phylogenetic study based on molecular data was carried out. Sequence data were compiled, combining data from all three genomes: nuclear ITS1 and 2, plastid trnS-rps4-trnT-trnL-trnF and rpl16, and mitochondrial nad5 intron. The Neckeraceae have sometimes been divided into the two families, Neckeraceae and Thamnobryaceae, a division rejected here. Both parsimony and Bayesian analyses of molecular data revealed that the family concept of the Neckeraceae needs several further adjustments, such as the exclusion of some individual species and smaller genera as well as the inclusion of the Leptodontaceae. Within the family three wellsupported clades (A, B and C) can be distinguished. Members of clade A are mainly non-Asiatic and nontropical. Most species have a weak costa and immersed capsules with reduced peristomes (mainly Neckera spp.) and the teeth at the leaf margins are usually unicellular. Clade B members are also mainly non-Asiatic. They are typically fairly robust, distinctly stipitate, having a single, at least relatively strong costa, long setae (capsules exserted), and the peristomes are well developed or only somewhat reduced. Members of clade C are essentially Asiatic and tropical. The species of this clade usually have a strong costa and a long seta, the seta often being mammillose in its upper part. The peristome types in this clade are mixed, since both reduced and unreduced types are found. Several neckeraceous genera that were recognised on a morphological basis are polyphyletic (e.g. Neckera, Homalia, Thamnobryum, Porotrichum). Ancestral state reconstructions revealed that currently used diagnostic traits, such as the leaf asymmetry and costa strength are highly homoplastic. Similarly, the reconstructions revealed that the 'reduced' sporophyte features have evolved independently in each of the three clades.

ABSTRACT. Phylogenetic analyses of the Hypnales usually show the same picture of poorly resolved trees with a large number of polyphyletic taxa and low support for the few reconstructed clades. One odd clade, however, consisting of three genera that are currently treated either within the Leskeaceae (Miyabea) or Neckeraceae (Homaliadelphus and Bissetia), was retrieved in a previously published phylogeny based on chloroplast rbcL. In order to elucidate the reliability of the observed Homaliadelphus -Miyabea -Bissetia -clade (HMB-clade) and to reveal its phylogenetic relationships a molecular study based on a representative set of hypnalean taxa was performed. Sequence data from all three genomes, namely the ITS1 and 2 (nuclear), the trnS-rps4-trnT-trnL-trnF cluster (plastid), the nad5 intron (mitochondrial), were analyzed. Although the phylogenetic reconstruction of the combined data set was not fully resolved regarding the backbone it clearly indicated the polyphyletic nature of various hypnalean families, such as the Leskeaceae, Hypnaceae, Hylocomiaceae, Neckeraceae, Leptodontaceae and Anomodontaceae with respect to the included taxa. In addition the results favor the inclusion of the Leptodontaceae and Thamnobryaceae in the Neckeraceae. The maximally supported HMB-clade consisting of the three genera Homaliadelphus (2-3 species), Miyabea (3 species) and Bissetia (1 species) is resolved sister to a so far unnamed clade comprising Taxiphyllum aomoriense, Glossadelphus ogatae and Leptopterigynandrum. The well-resolved and supported HMBclade, here formally described as the Miyabeaceae, fam. nov. is additionally supported by morphological characters such as strongly incrassate, porose leaf cells, a relatively weak and diffuse costa and the presence of dwarf males. The latter are absent in the Neckeraceae and the Leskeaceae. It is essentially an East Asian family, with one species occurring in North America.

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Leptodon corsicus (Neckeraceae) is described as the first endemic moss species from Corsica. It strikingly differs from the other species of the genus by the lack of a dense and pinnate to bipinnate mode of branching; about 10 times smaller shoots that do not inroll upon drying; the lack of paraphyllia; and few, occasional small pseudoparaphyllia. Due to its small size and several leaf characters, L. corsicus shares at first glance more similarities with Homalia webbiana and Neckera besseri than with Leptodon. Yet, phylogenetic analysis of chloroplast and nuclear DNA sequences unambiguously shows that L. corsicus is deeply nested within L. smithii. The numerous morphological characters that distinguish L. corsicus from L. smithii cannot be attributed to plasticity. Consequently, we interpret the phylogenetic position of L. corsicus as the result of a recent speciation process, involving mutations at one or a few coding loci or differences in gene expression, which have tremendous consequences for phenotypic appearance, and retention of ancestral polymorphism in the non-coding sequences used for phylogenetic reconstruction. Such an explanation might also apply to other species of mosses, which exhibit a striking morphology, and yet share identical non-coding sequences with the common species they derive from. The notion of species in mosses is discussed in this context.

Recent phylogenetic analyses indicated that the backbone phylogeny of the pleurocarpous moss family Neckeraceae falls into three distinct clades. Here the detailed composition and phylogenetic relationships of the two major clades (the Neckera clade and the Thamnobryum clade) are analysed. The phylogenetic analyses, based on sequence data from the plastid rpl16 intron and the rps4-trnT-trnL-trnF cluster as well as the nuclear ITS1 and 2, retained this tripartition and revealed a strong biogeographic pattern, especially inside the Neckera clade. In addition, several morphological characters that have been held as unique and characteristic to a certain group of mosses and therefore valuable in taxonomic classification, were shown to be highly homoplastic and subjected to convergent evolution. Consequently, the circumscriptions of Leptodon and Thamnobryum are amended, the new genera Exsertotheca, Echinodiopsis and Thamnomalia (each with two species), and Alleniella (with ten species) are formally described and several implied nomenclatural changes are proposed, including synonymisation of Alsia with Neckera and Cryptoleptodon with Leptodon.

The family Neckeraceae is composed of three distinct clades, of which two, i.e. the Neckera and Thamnobryum clades, are well defined. The third clade, consisting of species belonging to Caduciella, Curvicladium, Handeliobryum, Himantocladium, Homaliodendron, Hydrocryphaea, Neckera, Neckeropsis, Pinnatella, Shevockia and Taiwanobryum, is the focus of this study. Based on sequence data from the trnS-rps4-trnT-trnL-trnF plastid cluster and the rpl16 intron as well as from nuclear ITS1&2, the phylogenetic relationships of these genera are reconstructed. The nearest relatives of this clade are resolved shedding more light on the evolution of the family. The generic composition of the clade and its individual genera are discussed; polyphyly requires redefinition of Pinnatella, Neckeropsis and Homaliodendron. The positions of Touwia and Homalia within the family are addressed in an additional analysis based on more extensive sequence data, and the corresponding new combinations are made. Several further taxonomic changes are proposed, including Circulifolium gen. nov., comprising the former Homaliodendron exiguum and H. microdendron.